ID   MMU_12902_Cr2 standard; DNA; ROD; 1100 BP.
XX
AC   12902;
XX
DT   08-Sep-2005 (Created)
XX
DE   Cr2: complement receptor 2
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.1 195069923..195071022 (REVERSE)
CC   Score Points: 2 (66.7%)
CC   Chromosomal Location: 1 H6 / 1 106.6 cM
XX
CC   Database Reference MGI: 88489; Cr2
CC   Database Reference ENTREZGENE: 12902
CC   Database Reference UNIGENE: Mm.235387
CC   Database Reference UNIGENE: Mm.1226
CC   Database Reference ENSEMBL: ENSMUSG00000026616
CC   Database Reference REFSEQ: NM_007758
CC   Database Reference REFSEQ: NP_031784
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:102289_r_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:235387
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:Msa.549.0_s_at
CC   Database Reference TRANSFAC GENE: G005468; Cr2
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="1"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 195069923..195071022"
FT                   /note="Genomic Strand: REVERSE"
FT   prim_transcript 947..>947
FT                   /db_xref="ENSEMBL:ENSMUST00000082321"
FT   prim_transcript 1056..>1056
FT                   /db_xref="ENSEMBL:ENSMUST00000027917"
XX
SQ   Sequence 1100 BP; 306 A; 177 C; 248 G; 369 T; 0 other;
     gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtac gtgtgtgtgt        60
     gtggaggatg agggtttcta gaaaaagttt aatttctttc tctgtacctt tgatttatat       120
     attgtgactt cacacctatc aaaacaataa gaatagtacg gcattgtttc taataactct       180
     ataagtagtt ttgaacttct gtcatttttt aatacttttt gatggaatgg ttataatcac       240
     agaacattaa ctagtaaaat gatatcaata taacaggaat aaaaatcctt tatgtgtaat       300
     tttatgaatt tcttctctat ttacagacat taaataaatt tttcagtctt tattgttaat       360
     gtattgtgtt aacatatcag ttttatatat gaaaatatat agaaatatta atatatctct       420
     attgtaaaga ttttataatt gtaaatcttt tggggaaatg tcaatatgtc tttaaacttt       480
     aaagtgacaa atgtgatctc atttttctaa cattacggtc cgtcacaata aagacttaaa       540
     ggtgaaattc attttattcg acaaaagagt ttgactctca actaatgtaa ttaccccaaa       600
     ctttgactta attgaccttg ttttggggtt tgtccaaatt tcttatgtta tgacatttaa       660
     tcgtatagta tgctagtcat ccgtactcat aataaaacac tttaagaaca aagtctacat       720
     ccccccaccc ttgctctttc aattacatga accgacgagt tagttgtttt atatcctttc       780
     ggtccgcagc gtcttgggtc ggacttggtt ttcgtctgaa gggcccctgg cggggagaga       840
     cggagaaggc ggggatcagt ggacgtcaac acgaagtgtt tagaagtcat gggtcgcggt       900
     ggcgcgcctc ggctacgata aattcccaga cgaggggtga cgaatgtcgg tcggcgtccg       960
     tcggtcgggg cgtccgtcgg tcggggcagg agaaggagag gaacgatgtc cgagtgttga      1020
     gtgtctcgcg ttggacggta acctgacgac gtgtgtaccc taggaaccca agcgagaccc      1080
     aaaagaagtg agagtagtga                                                  1100
//
ID   MMU_12981_Csf2 standard; DNA; ROD; 1100 BP.
XX
AC   12981;
XX
DT   08-Sep-2005 (Created)
XX
DE   Csf2: colony stimulating factor 2 (granulocyte-macrophage)
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.11 53889284..53890383 (REVERSE)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 11 B1.3 / 11 29.5 cM
XX
CC   Database Reference MGI: 1339752; Csf2
CC   Database Reference ENTREZGENE: 12981
CC   Database Reference UNIGENE: Mm.4922
CC   Database Reference ENSEMBL: ENSMUSG00000018916
CC   Database Reference REFSEQ: NP_034099
CC   Database Reference REFSEQ: NM_009969
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:4922
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:GMCSF_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:92948_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:x03019_s_at
CC   Database Reference TRANSFAC GENE: G000517; GM-CSF
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="11"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 53889284..53890383"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     895..905
FT                   /note="TRANSFAC Site R00605"
FT   misc_signal     911..922
FT                   /note="TRANSFAC Site R01733"
FT   misc_signal     912..921
FT                   /note="TRANSFAC Site R00606"
FT   misc_signal     943..970
FT                   /note="TRANSFAC Site R05095"
FT                   /note="TRANSFAC Site R05096"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP11138"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: HSA [1437]; Alignment"
FT   prim_transcript 1003..>1003
FT                   /db_xref="ENSEMBL:ENSMUST00000019060"
XX
SQ   Sequence 1100 BP; 272 A; 260 C; 316 G; 252 T; 0 other;
     gcgcgcgcgt gtgcgtgtgt gcgtgcctgg ttattgtgtt acagctagtt actatgttac        60
     agccagcctc agagacccag gtatcccata atggtacaga tagcagtaat gtgtcctttt       120
     tgaatggcag gctgctctga agagggtaaa gaggctcaca taactcaaag gaagagtcgc       180
     ttggcaaagg gggagggcag aatcagcagt caaatgggag tagccttacc tgccccagcc       240
     agaagctcta gccatgctgt gaatttttag gattgaacat gcctttgtaa ctgggattgt       300
     agcagtcagt tgggatggta tcataagaga acatggtata gtctgcctgg cttctatacc       360
     cattgctgtc attctcactg ctcccaaggt ggcaggggtg gggcttggct gggcagagtt       420
     tgcccagaat ggtctcctca gtgggagtct gtggagacca ttatagaatt gtgtcattgg       480
     gctggacctt atttaattag ataatgaggt ggacttgtga gaagtgtata tctcagaagg       540
     tggctggaaa gagaacgggc caggactggg gctggaatga gccaccagag taggtagagc       600
     ttgcccaaag gcctccagga acagcaggtg ctatggaagc aagagcccca ctcagtatct       660
     cccaaacccc gccccagcca ctccaggcca ggaaatccaa atatgcctgg aggcccctca       720
     aaaaggagag gctagccaga ggctgggtca gactgcccag gcagggtggg aaaggccttt       780
     aaagcagccc gcaggtgggc tgccagttct tggaagggct tattaatgaa aaccccccaa       840
     gcctgacaac ctgggggaag gctcactggc cccatgtata gctgataagg gccaggagat       900
     tccacaactc aggtagttcc cccgcccccc tggagttctg tggtcaccat taatcatttc       960
     ctctaactgt gtatataaga gctcttttgc agtgagccca gtactcagag agaaaggcta      1020
     aggtcctgag gaggatgtgg ctgcagaatt tacttttcct gggcattgtg gtctacagcc      1080
     tctcagcacc cacccgctca                                                  1100
//
ID   MMU_14103_Fasl standard; DNA; ROD; 1100 BP.
XX
AC   14103;
XX
DT   09-Sep-2005 (Created)
XX
DE   Fasl: Fas ligand (TNF superfamily, member 6)
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.1 161800649..161801748 (REVERSE)
CC   Score Points: 2 (100.0%)
CC   Chromosomal Location: 1 H2.1 / 1 85.0 cM
XX
CC   Database Reference MGI: 99255; Fasl
CC   Database Reference ENTREZGENE: 14103
CC   Database Reference UNIGENE: Mm.3355
CC   Database Reference ENSEMBL: ENSMUSG00000000817
CC   Database Reference REFSEQ: NM_010177
CC   Database Reference REFSEQ: NP_034307
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:3355
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:97113_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubA:u06948_s_at
CC   Database Reference TRANSFAC GENE: G004128; Tnfsf6
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="1"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 161800649..161801748"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     744..755
FT                   /note="TRANSFAC Site R14691"
FT   misc_signal     938..959
FT                   /note="TRANSFAC Site R14661"
FT                   /note="TRANSFAC Site R14662"
FT   prim_transcript 976..>976
FT                   /db_xref="ENSEMBL:ENSMUST00000000834"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: HSA [356]; Alignment"
FT   misc_signal     1006..1027
FT                   /note="TRANSFAC Site R14663"
FT                   /note="TRANSFAC Site R14686"
FT   prim_transcript 1027..>1027
FT                   /db_xref="ENSEMBL:ENSMUST00000074892"
FT   misc_signal     1047..1057
FT                   /note="TRANSFAC Site R14690"
XX
SQ   Sequence 1100 BP; 302 A; 190 C; 310 G; 298 T; 0 other;
     aggcagcaga aaaataacac tttgggagtt gttttggcat aggtgagagg ggtagggtgc        60
     tcatcccaga aatcccaaag catgagataa aaaaaataaa accacttaaa atgtagagtc       120
     tgccaaaaag gtggaatata ggaacttatt gggatttata tggtttatat gggaaagtaa       180
     tgggaaccga gactgagttc ttagaggtta ttagacataa atggtgtgtg tgtgtgtgtg       240
     tgtgtggcca gaagacttgt gtgtgtgtgt gtgtgtgtgt gtgtgtggcc agaagacttg       300
     tgtgtgtgtg tgtgtgtgtg tggccagaag actgaagtca aacctaaggc agagtggtcg       360
     gttttataaa ggcataagat atatacttaa atttgttgta aatgttgaat aatgttttag       420
     tatgtgctgt gtgatggtta aggcacactt gctataaaaa tgctatttat tgcttatctc       480
     aaactcttct gaattaggca cctcagtttt catctggtga ccagaagaga gattgcaaag       540
     ttaaatgatt acagaggagg aaggctacat ttcccagggg aagtgggatg gatagggggc       600
     aggcacagtg gggggttagg gcagccttga acacctggca cacattcctg gttgcagctg       660
     gctgatgttc agggaaggga cttcaacaga ggattcaact ccctatgctc agatgtggag       720
     atatcttctc tagccgaact ccttggtctt ttccccatgc ctcagcacca acaggcctct       780
     caggacacac cccagagctg cggaagagct aatgtcctca aggggtatcc agcgctgact       840
     tgctgagttg gacctcaggc aggcaagcct ggtttaccag ccttctcagt tagcacagag       900
     acgccaattg gaacttcgaa gacttgtcgt cagaaatttc tgggcggaaa cttcctgggg       960
     ttgctgtgag ctttttgagg cttctcagct tcagatgcaa gtgagtgggt gtctcacaga      1020
     gaagcaaaga gaagagaaca ggagaaaggt gtttcccttg actgcggaaa ctttataaag      1080
     aaaacttagc ttctctggag                                                  1100
//
ID   HSA_1437_CSF2 standard; DNA; HUM; 1100 BP.
XX
AC   1437;
XX
DT   06-Sep-2005 (Created)
XX
DE   CSF2: colony stimulating factor 2 (granulocyte-macrophage)
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.5 131436381..131437480 (FORWARD)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 5q31.1
XX
CC   Database Reference HGNC: 2434; CSF2
CC   Database Reference ENTREZGENE: 1437
CC   Database Reference UNIGENE: Hs.1349
CC   Database Reference ENSEMBL: ENSG00000164400
CC   Database Reference REFSEQ: NP_000749
CC   Database Reference REFSEQ: NM_000758
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1400_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:210229_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210229_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1401_g_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210229_s_at
CC   Database Reference TRANSFAC GENE: G000272; GM-CSF
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="5"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 131436381..131437480"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     900..919
FT                   /note="TRANSFAC Site R00601"
FT                   /note="TRANSFAC Site R00602"
FT   misc_signal     929..958
FT                   /note="TRANSFAC Site R05031"
FT   misc_signal     936..965
FT                   /note="TRANSFAC Site R04957"
FT   misc_signal     938..942
FT                   /note="TRANSFAC Site R00603"
FT   misc_signal     942..965
FT                   /note="TRANSFAC Site R05033"
FT   misc_signal     947..970
FT                   /note="TRANSFAC Site R05034"
FT   misc_signal     952..956
FT                   /note="TRANSFAC Site R00603"
FT                   /note="TRANSFAC Site R00604"
FT   misc_signal     959..963
FT                   /note="TRANSFAC Site R00604"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP11137"
FT   misc_feature    1002
FT                   /note="SECONDARY ANCHOR: MMU [12981]; Alignment"
FT   prim_transcript 1004..>1004
FT                   /db_xref="ENSEMBL:ENST00000296871"
XX
SQ   Sequence 1100 BP; 237 A; 308 C; 326 G; 229 T; 0 other;
     cattgtgaaa atcaaacact tgtcagcccc tcaagagcct ttagatttcc tacttccaca        60
     cttccacaga aaggcctctg gagttggggg atgctggggt tatgtaggaa attaagcctg       120
     gagggccttg ctggggaagc cattgtccct gtacctgaga tggatgcagc cacagccctg       180
     gagccagcct gaagctcctg gtgtcttctg ggggctacat ataggagtgt agtccgaacc       240
     tcagaggggc aaacctgctc tgcagaggga atcaaggttc acataaccag agaggggagt       300
     cactcaggaa ggtggctcca gagccaagag tcagactctg ggtcccgact tgacccagcc       360
     acaccccctc tgaagcttgc tgagagtggc tgcagtctcg ctgctggatg tgcacatggt       420
     ggtcattccc tctgctcaca ggggcagggg tcccccctta ctggactgag gttgccccct       480
     gctccaggtc ctgggtggga gcccatgtga actgtcagtg gggcaggtct gtgagagctc       540
     ccctcacact caagtctctc acagtggcca gagaagagga aggctggagt cagaatgagg       600
     caccagggcg ggcatagcct gcccaaaggc ccctgggatt acaggcagga tggggagccc       660
     tatctaagtg tctcccacgc cccaccccag ccattccagg ccaggaagtc caaactgtgc       720
     ccctcagagg gagggggcag cctcaggccc attcagactg cccagggagg gctggagagc       780
     cctcaggaag gcgggtgggt gggctgtcgg ttcttggaaa ggttcattaa tgaaaacccc       840
     caagcctgac cacctaggga aaaggctcac cgttcccatg tgtggctgat aagggccagg       900
     agattccaca gttcaggtag ttcccccgcc tccctggcat tttgtggtca ccattaatca       960
     tttcctctgt gtatttaaga gctcttttgc cagtgagccc agtacacaga gagaaaggct      1020
     aaagttctct ggaggatgtg gctgcagagc ctgctgctct tgggcactgt ggcctgcagc      1080
     atctctgcac ccgcccgctc                                                  1100
//
ID   MMU_16160_Il12b standard; DNA; ROD; 1100 BP.
XX
AC   16160;
XX
DT   08-Sep-2005 (Created)
XX
DE   Il12b: interleukin 12b
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.11 44038798..44039897 (FORWARD)
CC   Score Points: 1 (100.0%)
CC   Chromosomal Location: 11 A5-B2 / 11 19.0 cM
XX
CC   Database Reference MGI: 96540; Il12b
CC   Database Reference ENTREZGENE: 16160
CC   Database Reference UNIGENE: Mm.997
CC   Database Reference UNIGENE: Mm.239707
CC   Database Reference ENSEMBL: ENSMUSG00000004296
CC   Database Reference REFSEQ: NP_032378
CC   Database Reference REFSEQ: NM_008352
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:100779_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubA:M86671_s_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:IL12_P40_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:239707
CC   Database Reference TRANSFAC GENE: G002345; IL-12 p40
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="11"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 44038798..44039897"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     859..894
FT                   /note="TRANSFAC Site R14483"
FT   misc_signal     891..932
FT                   /note="TRANSFAC Site R14479"
FT   misc_signal     913..938
FT                   /note="TRANSFAC Site R14477"
FT   misc_signal     924..955
FT                   /note="TRANSFAC Site R14475"
FT                   /note="TRANSFAC Site R14476"
FT   misc_signal     929..943
FT                   /note="TRANSFAC Site R14488"
FT   prim_transcript 1001..>1001
FT                   /db_xref="ENSEMBL:ENSMUST00000004407"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: RNO [64546]; Alignment"
FT   misc_feature    1015
FT                   /note="SECONDARY ANCHOR: HSA [3593]; Alignment"
XX
SQ   Sequence 1100 BP; 294 A; 254 C; 269 G; 283 T; 0 other;
     tcccaggagg cgggaaccca ggccagggac aggaatggag aagcggcggg ttgtgtccct        60
     tgcgtcccaa ccgcgaggat gtcctcgctt cgcgccctct atcggcggct ctgagagtgg       120
     ctctcatctg tatgcgaact ggatgtgcaa gaagagctaa tatttctgag cacggatgag       180
     gaagggaggt aacatcaact tacaggattg cacacctctt tgcaatttta aactcctcaa       240
     gaagagaaac tacaaagggt ttataggacc acagacacgt tattactgaa gtgagaatat       300
     agtatgggta cccaaaagag tgacctttga atcatctgta cgcttgccta tgtctagctc       360
     agttcatgct gctatcaatc catgagtaag gacctataag cataagagac gccctcaaaa       420
     cactatgact tttattagtt attcacctcc ccagagctgt ccctggatac agacaacata       480
     ggtatgaggt agggggtacg tggagccaaa caggaggtaa taccttctga atttagatgc       540
     taacaagaaa acatggggaa aggtggccca gatacactag gccctttatt ctttgggcct       600
     gtaacaccta cttatttgat tgtggcatga accatgaact cggtttgggg caagtccttc       660
     ctttttctgc agtctgtgga atcgggagag gttagccatt gccgcctcta ttcaccttag       720
     gcatgatgta aacagaaatt agtatctctg cctccttcct ttttccacac cccgaagtca       780
     tttcctctta acctgggatt tcgacgtcta tattccctct gtatgataga tgcactcagg       840
     gaggcaaggg ggggagggag gaacttctta aaattccccc agaatgtttt gacactagtt       900
     ttcagtgttg caattgagac tagtcagttt ctactttggg tttccatcag aaagttctgt       960
     aggagtagag tatataagca ccaggagcag ccaaggcagc agaaggaaca gtgggtgtcc      1020
     aggcacatca gaccaggcag ctcgcagcaa agcaaggtaa gttctctcct cttccctgtc      1080
     gctaactccc tgcatctaga                                                  1100
//
ID   MMU_16183_Il2 standard; DNA; ROD; 1100 BP.
XX
AC   16183;
XX
DT   08-Sep-2005 (Created)
XX
DE   Il2: interleukin 2
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.3 36927598..36928697 (REVERSE)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 3 B-C / 3 19.2 cM
XX
CC   Database Reference MGI: 96548; Il2
CC   Database Reference ENTREZGENE: 16183
CC   Database Reference UNIGENE: Mm.14190
CC   Database Reference ENSEMBL: ENSMUSG00000027720
CC   Database Reference REFSEQ: NM_008366
CC   Database Reference REFSEQ: NP_032392
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubA:m16762_s_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:102705_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:AFFX-MurIL2_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Bv2:AFFX-MurIL2_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Cv2:AFFX-MurIL2_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:IL2_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:14190
CC   Database Reference TRANSFAC GENE: G000533; IL-2
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="3"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 36927598..36928697"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     146..175
FT                   /note="TRANSFAC Site R13237"
FT   misc_signal     183..212
FT                   /note="TRANSFAC Site R13238"
FT   misc_signal     721..737
FT                   /note="TRANSFAC Site R02348"
FT                   /note="TRANSFAC Site R05036"
FT                   /note="TRANSFAC Site R14645"
FT   misc_signal     781..790
FT                   /note="TRANSFAC Site R03696"
FT   misc_signal     791..815
FT                   /note="TRANSFAC Site R02951"
FT   misc_signal     833..842
FT                   /note="TRANSFAC Site R03697"
FT   misc_signal     840..865
FT                   /note="TRANSFAC Site R02952"
FT                   /note="TRANSFAC Site R05049"
FT   misc_signal     868..885
FT                   /note="TRANSFAC Site R02349"
FT                   /note="TRANSFAC Site R05050"
FT   misc_signal     910..942
FT                   /note="TRANSFAC Site R02953"
FT   misc_signal     911..927
FT                   /note="TRANSFAC Site R05051"
FT                   /note="TRANSFAC Site R05052"
FT   misc_signal     953..963
FT                   /note="TRANSFAC Site R05053"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP11136"
FT   prim_transcript 1006..>1006
FT                   /db_xref="ENSEMBL:ENSMUST00000029275"
XX
SQ   Sequence 1100 BP; 375 A; 257 C; 176 G; 292 T; 0 other;
     aaggtgacag gagagaagtt actagcaaga gttggtctct gacctccaca ggtgtactgt        60
     ggcacacaca cacacacaca ctcataatac atgtgcacaa atgcatgtac acatacatac       120
     acacatgcat acatgcacac acacacactc atatacacac gcacataaac atgctcacac       180
     acacatacat gtgcacgcac atgcacatac tcatacacac atgaacacat gtgtgtgtac       240
     acacgtgaaa atatttttta aaaatgaaag tgcaactaga gacatataaa ataacaccaa       300
     catccttaga tgcaaccctt cctgagaatt tgttggacat catactcttt ttaaaaagca       360
     taataaacat caagacactt acacaaaata tgttaaatta aatttaaaac aacaacgaca       420
     aaatagtacc tcaagctcaa caagcatttt aggtgtcctt agcttactat ttctctggct       480
     aactgtatga agccatctat caccctgtgt gcaattagct cattgtgtag ataagaaggt       540
     aaaaccatct tgaaacagga aaccaatatc cttcctgtct aatcaacaaa tctaaaagat       600
     ttattctttt catctatctc ctcttgcgtt tgtccaccac aacaggctgc ttacaggttc       660
     aggatggttt tgacaaagag aacattttca tgagttactt ttgtgtctcc accccaaaga       720
     ggaaaatttg tttcatacag aaggcgttca ttgtatgaat taaaactgcc acctaagtgt       780
     gggctaaccc gaccaagagg gatttcacct aaatccattc agtcagtgta tgggggttta       840
     aagaaattcc agagagtcat cagaagagga aaaacaaagg taatgctttc tgccacacag       900
     gtagactctt tgaaaatatg tgtaatatgt aaaacatcgt gacaccccca tattattttt       960
     ccagcattaa cagtataaat tgcctcccat gctgaagagc tgcctatcac ccttgctaat      1020
     cactcctcac agtgacctca agtcctgcag gcatgtacag catgcagctc gcatcctgtg      1080
     tcacattgac acttgtgctc                                                  1100
//
ID   MMU_16189_Il4 standard; DNA; ROD; 1100 BP.
XX
AC   16189;
XX
DT   08-Sep-2005 (Created)
XX
DE   Il4: interleukin 4
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.11 53258309..53259408 (REVERSE)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 11 B1.3 / 11 29.0 cM
XX
CC   Database Reference MGI: 96556; Il4
CC   Database Reference ENTREZGENE: 16189
CC   Database Reference UNIGENE: Mm.371
CC   Database Reference UNIGENE: Mm.276360
CC   Database Reference ENSEMBL: ENSMUSG00000000869
CC   Database Reference REFSEQ: NM_021283
CC   Database Reference REFSEQ: NP_067258
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:92286_g_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:276360
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubA:m13238_s_at
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:IL4_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:AFFX-MurIL4_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:92283_s_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Bv2:AFFX-MurIL4_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Cv2:AFFX-MurIL4_at
CC   Database Reference TRANSFAC GENE: G000534; IL-4
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="11"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 53258309..53259408"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     840..852
FT                   /note="TRANSFAC Site R08172"
FT   misc_signal     909..944
FT                   /note="TRANSFAC Site R05081"
FT   misc_signal     913..922
FT                   /note="TRANSFAC Site R05079"
FT   misc_signal     926..940
FT                   /note="TRANSFAC Site R05080"
FT   misc_signal     937..951
FT                   /note="TRANSFAC Site R04080"
FT   misc_signal     941..972
FT                   /note="TRANSFAC Site R04775"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP15039"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: HSA [3565]; Alignment"
FT   prim_transcript 1026..>1026
FT                   /db_xref="ENSEMBL:ENSMUST00000000889"
XX
SQ   Sequence 1100 BP; 279 A; 259 C; 261 G; 301 T; 0 other;
     ctgctggtgg ggggcaatga gtacctcgac agggcctgca ttcgttagat taaggcagtg        60
     ggctgggggc agggtgctga ctgagagggt gagagagggc tgtttcctgg ttagtgaagg       120
     atatgtttta agttcattga aaaggcagcc agccattctt gggccaatga gatggctcag       180
     gagggaaggt gcttgccgcc aagcttgtga gtctgagttc aaggatccac acggtgcaaa       240
     gagagacccg gtctcctgac ctccacactg atgctgtagt gcacatagat acacacatgc       300
     tcacatgaag taatttaaaa aaattttttt ttaaatcagc catttctcag gcttctgtct       360
     aaggtaggaa aaatcttcaa cctagcccag aacctccata taggtaaagc ctcattccat       420
     ggtcctgcct gccccactcc atgtcacctc tctgtctcca aagaccacaa acttgtaaga       480
     tcagctggtc taggatgcga gaaggtctgc ctccatcatc cttctatgag gtaagacccc       540
     agagtcagct ttcccaagat atcagagttt ccaaggggcc cccatagcag gaagcagcta       600
     ggcccaggtg tgctcaaggc agactttctt gatattactc tgtctttccc cagggcgaca       660
     ccagcaccct cggacacctg tgacctcttc cttctctgca ggaggagagc cagtggcaac       720
     cctacgctga taagattagt ctgaaaggcc gattatggtg taatttccta tgctgaaact       780
     ttgtagattt aaaaaaaaag gggggggagg ggtgtttcat tttccaattg gtctgatttc       840
     acaggaaaat ttacctgttt ctcttttttc tcctggaaga gaggtgctga ttggcccaga       900
     ataactgaca atctggtgta ataaaatttt ccaatgtaaa ctcattttcc cttggtttca       960
     gcaactttaa ctctatatat agagagacct ctgccagcat tgcattgtta gcatctcttg      1020
     ataaacttaa ttgtctctcg tcactgacgg cacagagcta ttgatgggtc tcaaccccca      1080
     gctagttgtc atcctgctct                                                  1100
//
ID   MMU_16191_Il5 standard; DNA; ROD; 1100 BP.
XX
AC   16191;
XX
DT   08-Sep-2005 (Created)
XX
DE   Il5: interleukin 5
XX
OS   Mus musculus (mouse)
XX
CC   Build MMU_May2004: Chr.11 53359533..53360632 (FORWARD)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 11 A5 / B1 / 11 29.2 cM
XX
CC   Database Reference MGI: 96557; Il5
CC   Database Reference ENTREZGENE: 16191
CC   Database Reference UNIGENE: Mm.4461
CC   Database Reference ENSEMBL: ENSMUSG00000036117
CC   Database Reference REFSEQ: NM_010558
CC   Database Reference REFSEQ: NP_034688
CC   Database Reference AFFYMETRIX: AFFY_MG_U74Av2:98374_at
CC   Database Reference AFFYMETRIX: AFFY_MG_U74:4461
CC   Database Reference AFFYMETRIX: AFFY_Mu11KsubB:x06271_s_at
CC   Database Reference TRANSFAC GENE: G000535; IL-5
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="11"
FT                   /organism="Mus musculus (mouse)"
FT                   /note="Genomic Sequence Build: MMU_May2004"
FT                   /note="Genomic Positions: 53359533..53360632"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     883..908
FT                   /note="TRANSFAC Site R05097"
FT                   /note="TRANSFAC Site R05098"
FT   misc_signal     911..922
FT                   /note="TRANSFAC Site R08263"
FT   misc_signal     926..945
FT                   /note="TRANSFAC Site R08264"
FT   misc_signal     946..960
FT                   /note="TRANSFAC Site R04079"
FT   misc_signal     970..984
FT                   /note="TRANSFAC Site R08262"
FT   misc_feature    1000
FT                   /note="SECONDARY ANCHOR: HSA [3567]; Alignment"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP25045"
FT                   /db_xref="ENSEMBL:ENSMUST00000048605"
XX
SQ   Sequence 1100 BP; 310 A; 241 C; 232 G; 317 T; 0 other;
     caggagtcct gttgtcaccc tggagcaccc ctcatacaca cagtaagctg cttgaaaagt        60
     gggtcaaggc caagccacca aagcagtaca ggaaggagcc tctgccctgc actttttgtc       120
     ataggaacca agaagcatcc tcttatctcc actcagtctg ggttggcctt ttagtaacag       180
     acaggatgct gatcaaaaac ctacatcatg caactcaact ctgtcagacc agctgcttta       240
     ataaatgtct ttcccagaga gttttcaatt ctttttttct tttctttttt taagcacaga       300
     taagtctagc taccgccaat atagaaaaaa aaacaccccc tttccctttt ctctttggca       360
     gtttggagca gggtcttgtg tgttccagat tgaactcacc tttgctgtac acacaaaaaa       420
     gccaaagatg ctgtcacctc ttgatcctcc tgactgtacc tcccacatct gctggtgtgt       480
     accaccacac ctagtaagat attctcaaca tttatgtatt ttagcctaac cctgttggag       540
     gtatacattt gaatacattt tttctcactt tatcaggaat tgagtttaac acatattaaa       600
     gcaggtgtgg ggcagggagg gggggataaa aaagaaggtg ctcaagaaaa gccgatcacg       660
     ctcccaagag tgtgagcatg ggcgtctcta gagagatccg ccatatatgc acaactttta       720
     aagagaaatt caataaccag aatggagtgt aaatgtggat caaagttgta gaaacattct       780
     tttatgttat agaaaatgct ttttaagcag gggtgggggt caagatgtta actattatta       840
     aagagcaaaa aaaaaaaaat gcattttgtt tgaagaccca gggcactgga aaccctgagt       900
     ttcaggactc gcctttatta ggtgtcctct atctgattgt tagcaattat tcatttcctc       960
     agagagagaa taaattgctt ggggattcgg ccctgctctg cgctcttcct ttgctgaagg      1020
     ccagcgctga agacttcaga gtcatgagaa ggatgcttct gcacttgagt gttctgactc      1080
     tcagctgtgt ctgggccact                                                  1100
//
ID   HSA_1960_EGR3 standard; DNA; HUM; 1100 BP.
XX
AC   1960;
XX
DT   05-Sep-2005 (Created)
XX
DE   EGR3: early growth response 3
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.8 22606661..22607760 (REVERSE)
CC   Score Points: 1 (33.3%)
CC   Chromosomal Location: 8p23-p21
XX
CC   Database Reference HGNC: 3240; EGR3
CC   Database Reference ENTREZGENE: 1960
CC   Database Reference UNIGENE: Hs.534313
CC   Database Reference ENSEMBL: ENSG00000179388
CC   Database Reference REFSEQ: NP_004421
CC   Database Reference REFSEQ: NM_004430
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206115_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206115_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40375_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:206115_at
CC   Database Reference TRANSFAC GENE: G004597; Egr3
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="8"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 22606661..22607760"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     689..715
FT                   /note="TRANSFAC Site R13414"
FT   prim_transcript 1001..>1001
FT                   /db_xref="ENSEMBL:ENST00000317216"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: MMU [13655]; Alignment"
FT                   /note="PRIMARY ANCHOR: RNO [25148]; Alignment"
XX
SQ   Sequence 1100 BP; 184 A; 360 C; 319 G; 237 T; 0 other;
     tcattctttc ctcttcacca cgaaaaccgc acatcctcga ccccatatgg atggggctct        60
     tgtctttggc gcaactgctg gggtgctccg aatctcctcg ccactgcgct cagcctagag       120
     tcagcgccgg gtcaggggcc cagggagggg caggggcggc gaatcagagt gaagttggca       180
     caaaagttct tgggatattg gaccaaggaa ttctgacaag ttgaaacacc cccccaaccc       240
     tgcgcgcacc cctccttccc cccacaaagg gaagcactcc ctttctctta atctcggata       300
     ggatcccgaa cgctggagcc gctgaggtag caggggcgca acgcacgcct tccgggttcc       360
     ccagcagttc ccgggctgca aagggatttc gccagatgtt ttcaactctc tttctaactg       420
     ctggggtgtt ggagaccact tgcaaacaac cccaccccac cgcccacctc tccccaatgc       480
     gctctcctaa cgcaaacctc aaataaacac acacaatgag ttactggtgt ttcgactcca       540
     cgctacgcgc tttgcgcttt gcatgcagct gtatccttct ttcctctctc ttctcgcatt       600
     cttcttgttt cttctcccct tctctttttt tcaagagccg cgagcggtgc gggcgccgca       660
     cgttggctgc ggcccgcttc ctgctttcta atgttccatt gtgaggagct tccattgtga       720
     cgtcgcgccc cttcggctgg gctttgtctg tccatatatg ggcagctacg tcacggagct       780
     ttcccggggc tcagataaat aggctggtgg agttccctgg ctgggagctt ttgggcagca       840
     gtgagcttgc taggaagcgg cggggctggt ggtggtggta gcagcggcgg cagcggcggc       900
     agaggcggcg gcggcggcgg cggcggcggc ggcggtggcg gtggcggtgg cggtggcaga       960
     tcggggggcg ggggggcggc gggcgcgtgt ctgtttgtga gatcaatact gaggccgcgt      1020
     ccgaccccct tgagccgaga tcccccccca gcccagcccc caccccaccc cccgcacacg      1080
     ccccaccccc cccacgaccc                                                  1100
//
ID   RNO_24505_Ins1 standard; DNA; ROD; 1100 BP.
XX
AC   24505;
XX
DT   05-Sep-2005 (Created)
XX
DE   Ins1: insulin 1
XX
OS   Rattus norvegicus (rat)
XX
CC   Build RNO_Nov2004: Chr.1 258000122..258001221 (FORWARD)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 1q54-q55
XX
CC   Database Reference RGNC: 2915; Ins1
CC   Database Reference ENTREZGENE: 24505
CC   Database Reference UNIGENE: Rn.962
CC   Database Reference ENSEMBL: ENSRNOG00000012052
CC   Database Reference REFSEQ: NM_019129
CC   Database Reference REFSEQ: NP_062002
CC   Database Reference AFFYMETRIX: AFFY_RG_U34B:rc_C07167_f_at
CC   Database Reference TRANSFAC GENE: G000760; ins-1
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="1"
FT                   /organism="Rattus norvegicus (rat)"
FT                   /note="Genomic Sequence Build: RNO_Nov2004"
FT                   /note="Genomic Positions: 258000122..258001221"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     671..693
FT                   /note="TRANSFAC Site R08705"
FT   misc_signal     684..690
FT                   /note="TRANSFAC Site R00898"
FT   misc_signal     702..710
FT                   /note="TRANSFAC Site R13243"
FT   misc_signal     753..803
FT                   /note="TRANSFAC Site R08849"
FT   misc_signal     761..770
FT                   /note="TRANSFAC Site R00902"
FT   misc_signal     762..769
FT                   /note="TRANSFAC Site R00900"
FT   misc_signal     778..792
FT                   /note="TRANSFAC Site R00901"
FT   misc_signal     778..794
FT                   /note="TRANSFAC Site R00903"
FT   misc_signal     810..824
FT                   /note="TRANSFAC Site R00905"
FT   misc_signal     832..847
FT                   /note="TRANSFAC Site R00907"
FT   misc_signal     885..896
FT                   /note="TRANSFAC Site R00910"
FT   misc_signal     887..895
FT                   /note="TRANSFAC Site R00908"
FT   misc_signal     888..895
FT                   /note="TRANSFAC Site R00909"
FT   misc_signal     944..966
FT                   /note="TRANSFAC Site R04623"
FT   prim_transcript 998..>998
FT                   /db_xref="EPD:EP11131"
FT   misc_feature    998
FT                   /note="PRIMARY ANCHOR: MMU [16333]; Alignment"
FT                   /note="SECONDARY ANCHOR: RNO [24506]; Alignment"
FT                   /note="SECONDARY ANCHOR: MMU [16333]; Alignment"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: MMU [16333]; Alignment"
FT                   /note="SECONDARY ANCHOR: RNO [24506]; Alignment"
XX
SQ   Sequence 1100 BP; 303 A; 248 C; 241 G; 308 T; 0 other;
     ttttaaaagc tttcatggat ggcactggag aagttaaatt tttttgctgt ataacctatg        60
     tttattttat accataagga cttcacaaac taacttaacg ttattggacc agtacaaacc       120
     tactttcttt aatggcttct gagttacttg aagacaagta acgtgtctac tttattatgg       180
     cgcctacatt ggaacccact gcgcatcacc agagattttt ctcagcaaat gtttgttgac       240
     ttaattgaat gctgtcattg acagaaagtc tggtttgcat ttcctctcaa ctccttgaaa       300
     atagctacct ttcctaattg accctgttgg cagatgttta aactggggtg aacgctgtgc       360
     tactgaggcc tgatgctttg tggaaaatca attagaatga gaccaaatgt tccacctaat       420
     tcaaatggtt gtcaaaaaat agaatttgag tatctatatt tcgtcccagc tgacccctga       480
     gtgggctatg ggtttgtgga agtagagata gaggagaagg gaccattaca tgtcctgctg       540
     cctgagttct gctttccttc tccctttgaa ggtgagctgg ggtctcagct gagctaagaa       600
     tccagctatc aatagaaact atgaaacagt tccagggaca aagataccag gtccccaaca       660
     actgcaactt tctgggaaat gaggtggaaa atgctcagcc aaggaaaaag agggccttac       720
     cctctctggg acaatgattg tgctgtgaac tgcttcatca ggccatctgg ccccttgtta       780
     ataatctaat taccctaggt ctaagtagag ttgttgacgt ccaatgagcg ctttctgcag       840
     acttagcact aggcaagtgt ttggaaatta cagcttcagc ccctctcgcc atctgcctac       900
     ctacccctcc tagagccctt aatgggccaa acggcaaagt ccagggggca gagaggaggt       960
     gctttggact ataaagctag tggagaccca gtaactccca accctaagtg accagctaca      1020
     atcatagacc atcagcaagc aggtatgtac tctcctgggt gagcccggtt cccccagcca      1080
     aaactctagg gactttagga                                                  1100
//
ID   RNO_24952_Gcg standard; DNA; ROD; 1100 BP.
XX
AC   24952;
XX
DT   05-Sep-2005 (Created)
XX
DE   Gcg: glucagon
XX
OS   Rattus norvegicus (rat)
XX
CC   Build RNO_Nov2004: Chr.3 44440955..44442054 (REVERSE)
CC   Score Points: 50 (98.0%)
CC   Chromosomal Location: 3q22-q24
XX
CC   Database Reference RGNC: 2668; Gcg
CC   Database Reference ENTREZGENE: 24952
CC   Database Reference UNIGENE: Rn.54383
CC   Database Reference ENSEMBL: ENSRNOG00000005498
CC   Database Reference REFSEQ: NM_012707
CC   Database Reference REFSEQ: NP_036839
CC   Database Reference TRANSFAC GENE: G000741; GLUC
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="3"
FT                   /organism="Rattus norvegicus (rat)"
FT                   /note="Genomic Sequence Build: RNO_Nov2004"
FT                   /note="Genomic Positions: 44440955..44442054"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     697..718
FT                   /note="TRANSFAC Site R02456"
FT   misc_signal     733..763
FT                   /note="TRANSFAC Site R14770"
FT                   /note="TRANSFAC Site R14771"
FT   misc_signal     733..764
FT                   /note="TRANSFAC Site R00580"
FT   misc_signal     736..756
FT                   /note="TRANSFAC Site R08704"
FT   misc_signal     736..770
FT                   /note="TRANSFAC Site R08703"
FT   misc_signal     801..836
FT                   /note="TRANSFAC Site R00581"
FT                   /note="TRANSFAC Site R13436"
FT   misc_signal     900..937
FT                   /note="TRANSFAC Site R00582"
FT   misc_signal     901..949
FT                   /note="TRANSFAC Site R08777"
FT   misc_signal     906..932
FT                   /note="TRANSFAC Site R15435"
FT   misc_signal     928..952
FT                   /note="TRANSFAC Site R08875"
FT                   /note="TRANSFAC Site R15436"
FT   misc_signal     941..965
FT                   /note="TRANSFAC Site R15432"
FT   misc_signal     975..979
FT                   /note="TRANSFAC Site R00583"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP17066"
XX
SQ   Sequence 1100 BP; 337 A; 238 C; 218 G; 307 T; 0 other;
     gctgtggtga tcttgtcata tagaatatga gtttcatttt aaacaaatgt ttacacaaat        60
     caatgcttct cacaaatcag caacagagtc ccaaagactg tgtggcttgg ccacggtctc       120
     atagcctatt gatgatagca gggaagaaaa atctacttat gatccccgga gtttcttgct       180
     gtctgttcac acatcctggt tatttcccaa ttttatttcc ttctgttgaa atggccagaa       240
     ttgtatctgc tacatactat aattagtaag gacctatata cgtgctggaa gttacagaaa       300
     gtaacagcat gcatctcaga ccaatagttt gcctcccatg tctttctttg tattctaatg       360
     tcacacccct tctcagtgaa attagattta aaacatttcg aaagatgaaa aagaaataat       420
     agaccctttg ctatcagcat cagtgacgtt gggtattctc attttgcctt ctgtgtctca       480
     ttaacatagt gcacattaca ttttaattga catttaaaat ctccccacaa agagagtaca       540
     aattcattcc atacaaagta gatgagtggg ttattgatat gtgtgcactg ggtgagcgat       600
     ttgtttgcct agatgaatgg tccatcagtt attcaggaac tcaggatggc caaatagcac       660
     atcaagggac aagaccctca aatgactcct ctaggctcat ttgacgtcaa aattcacttc       720
     agagagctga agtagttttt cacgcctgac tgagattgaa gggtgtattt ccaaactacc       780
     ctttccattc ccaaacagaa aggcacaaga gtaaataaaa agtttccggg cctctgaggt       840
     ctcaccccgg tatcagcgtg aggagcagat gagcagagtg ggcgagtgaa atcatttgaa       900
     caaaacccca ttatttacag atgagaaatt tatattgtca gcgtaatatc tgcaaggcta       960
     aacagcctgg agactatata aaagcacagc accctggtgc agaagggcag agcttgggcg      1020
     cagaacacac tcaaagttcc caaaggagct ccacctgtct acacctcctc tcagctcagt      1080
     cccacaaggt aagaggcaca                                                  1100
//
ID   HSA_3383_ICAM1 standard; DNA; HUM; 1100 BP.
XX
AC   3383;
XX
DT   05-Sep-2005 (Created)
XX
DE   ICAM1: intercellular adhesion molecule 1 (CD54), human rhinovirus
DE   receptor
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.19 10241789..10242888 (FORWARD)
CC   Score Points: 97 (89.8%)
CC   Chromosomal Location: 19p13.3-p13.2
XX
CC   Database Reference HGNC: 5344; ICAM1
CC   Database Reference ENTREZGENE: 3383
CC   Database Reference UNIGENE: Hs.515126
CC   Database Reference ENSEMBL: ENSG00000090339
CC   Database Reference REFSEQ: NM_000201
CC   Database Reference REFSEQ: NP_000192
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202638_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207194_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215485_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:215485_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:202637_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35078_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:202638_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32640_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:215485_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207194_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202637_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207194_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202638_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202637_s_at
CC   Database Reference TRANSFAC GENE: G001071; ICAM-1
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="19"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 10241789..10242888"
FT                   /note="Genomic Strand: FORWARD"
FT   prim_transcript 729..>729
FT                   /db_xref="dbTSS:SYN09326"
FT   misc_signal     805..822
FT                   /note="TRANSFAC Site R08087"
FT   misc_signal     817..837
FT                   /note="TRANSFAC Site R08088"
FT                   /note="TRANSFAC Site R13475"
FT   prim_transcript 882..>882
FT                   /db_xref="dbTSS:LFL02065"
FT   prim_transcript 902..>902
FT                   /db_xref="dbTSS:LFL09295"
FT                   /note="Number of reported TSSs: 3"
FT   prim_transcript 970..>970
FT                   /db_xref="dbTSS:T3R05169"
FT   prim_transcript 977..>977
FT                   /db_xref="ENSEMBL:ENST00000264832"
FT   prim_transcript 998..>998
FT                   /db_xref="dbTSS:SPL05195"
FT                   /note="Number of reported TSSs: 5"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: MMU [15894]; Alignment"
FT                   /note="PRIMARY ANCHOR: RNO [25464]; Alignment"
FT   prim_transcript 1005..>1005
FT                   /db_xref="dbTSS:MPG01568"
FT   prim_transcript 1007..>1007
FT                   /db_xref="dbTSS:CAS10961"
FT                   /note="Number of reported TSSs: 2"
FT   prim_transcript 1008..>1008
FT                   /db_xref="EPD:EP73783"
FT   misc_feature    1008
FT                   /note="PRIMARY ANCHOR: MMU [15894]; Alignment"
FT                   /note="PRIMARY ANCHOR: RNO [25464]; Alignment"
FT   prim_transcript 1009..>1009
FT                   /db_xref="dbTSS:LFL03104"
FT                   /note="Number of reported TSSs: 3"
FT   prim_transcript 1028..>1028
FT                   /db_xref="dbTSS:LFL05106"
FT   misc_feature    1046
FT                   /note="SECONDARY ANCHOR: RNO [25464]; Alignment"
FT   misc_feature    1048
FT                   /note="SECONDARY ANCHOR: MMU [15894]; Alignment"
XX
SQ   Sequence 1100 BP; 189 A; 345 C; 360 G; 206 T; 0 other;
     tttagtgcat gagcctgggt tcgagttgcc ggagcctcgc gcgtagggca ggggttcgag        60
     cgccccttct ccctgcctcg cctctgcgcc tgggggctgc tgcctcagtt tcccagcgac       120
     aggcagggat ttcgagcgtc cccctcccct ccctcgtcaa gatccaagct agctgcctca       180
     gtttccccgc ggagcctggg acgccagcgg aggggctcgg cgcgtaggga tcacgcagct       240
     tccttccttt ttctgggagc tgtaaagacg cctccgcggc caaggccgaa aggggaagcg       300
     aggaggccgc cggggtgagt gccctcgggt gtagagagag gacgccgatt tccccggacg       360
     tggtgagacc gcgcttcgtc actcccacgg ttagcggtcg ccgggaggtg cctggctctg       420
     ctctggccgc ttctcgagaa atgcccgtgt cagctaggtg tggacgtgac ctagggggag       480
     gggcatccct cagtggaggg agcccgggga ggattcctgg gcccccaccc aggcaggggg       540
     ctcatccact cgattaaaga ggcctgcgta agctggagag ggaggacttg agttcggacc       600
     ccctcgcagc ctggagtctc agtttaccgc tttgtgaaat ggacacaata acagtctcca       660
     ctctccgggg aagttggcag tatttaaaag tacttaataa accgcttagc gcggtgtaga       720
     ccgtgattca agcttagcct ggccgggaaa cgggaggcgt ggaggccggg agcagccccc       780
     ggggtcatcg ccctgccacc gccgcccgat tgctttagct tggaaattcc ggagctgaag       840
     cggccagcga gggaggatga ccctctcggc ccgggcaccc tgtcagtccg gaaataactg       900
     cagcatttgt tccggagggg aaggcgcgag gtttccggga aagcagcacc gccccttggc       960
     ccccaggtgg ctagcgctat aaaggatcac gcgccccagt cgacgctgag ctcctctgct      1020
     actcagagtt gcaacctcag cctcgctatg gctcccagca gcccccggcc cgcgctgccc      1080
     gcactcctgg tcctgctcgg                                                  1100
//
ID   HSA_3458_IFNG standard; DNA; HUM; 1100 BP.
XX
AC   3458;
XX
DT   05-Sep-2005 (Created)
XX
DE   IFNG: interferon, gamma
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.12 66839691..66840790 (REVERSE)
CC   Score Points: 51 (100.0%)
CC   Chromosomal Location: 12q14
XX
CC   Database Reference HGNC: 5438; IFNG
CC   Database Reference ENTREZGENE: 3458
CC   Database Reference UNIGENE: Hs.856
CC   Database Reference ENSEMBL: ENSG00000111537
CC   Database Reference REFSEQ: NP_000610
CC   Database Reference REFSEQ: NM_000619
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:210354_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210354_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1611_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40702_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1021_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210354_at
CC   Database Reference TRANSFAC GENE: G001174; IFN-gamma
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="12"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 66839691..66840790"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     209..225
FT                   /note="TRANSFAC Site R13473"
FT   misc_signal     222..237
FT                   /note="TRANSFAC Site R13474"
FT   misc_signal     715..734
FT                   /note="TRANSFAC Site R08184"
FT                   /note="TRANSFAC Site R13472"
FT   misc_signal     757..792
FT                   /note="TRANSFAC Site R04952"
FT   misc_signal     793..817
FT                   /note="TRANSFAC Site R04951"
FT   misc_signal     835..847
FT                   /note="TRANSFAC Site R08183"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP07113"
FT                   /db_xref="ENSEMBL:ENST00000229135"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: MMU [15978]; Alignment"
FT                   /note="PRIMARY ANCHOR: RNO [25712]; Alignment"
XX
SQ   Sequence 1100 BP; 333 A; 229 C; 203 G; 335 T; 0 other;
     ccaccttctg ggttcaagcc attctcctgc ctcagcctcc ctagtagctg agattacagg        60
     catacaccac catgcctggc taattttttt gtatttttag tagagatggg gtttcaccat       120
     attggctagg ctggtctcaa actcctgacc ttgtgatcca cccgcctcaa cctcccaaag       180
     tgctgggatt acaggtgtga gccactgcgt ctggaactcc ccctgggaat attctctaca       240
     ctgtatttca aggatttaat atgacaaaaa gaatgtcaaa taccttatta acaatgtagt       300
     atattgatgc atactgaagt actatttggg atatattggt ttaaatacaa tatattttaa       360
     aattatattt accttttaaa aaaactttta ttaatgaggc tactagatca tttaaattta       420
     cctgtgtggc ttgtattgta tttctactgg gcagtgctga tctagagcaa tttgaaactt       480
     gtggtagata ttttactaac caactctgat gaaggacttc ctcaccaaat tgttctttta       540
     accgcattct ttccttgctt tctggtcatt tgcaagaaaa attttaaaag gctgcccctt       600
     tgtaaaggtt tgagaggccc tagaatttcg tttttcactt gttcccaacc acaagcaaat       660
     gatcaatgtg ctttgtgaat gaagagtcaa cattttacca gggcgaagtg gggaggtaca       720
     aaaaaatttc cagtccttga atggtgtgaa gtaaaagtgc cttcaaagaa tcccaccaga       780
     atggcacagg tgggcataat gggtctgtct catcgtcaaa ggacccaagg agtctaaagg       840
     aaactctaac tacaacaccc aaatgccaca aaaccttagt tattaataca aactatcatc       900
     cctgcctatc tgtcaccatc tcatcttaaa aaacttgtga aaatacgtaa tcctcaggag       960
     acttcaatta ggtataaata ccagcagcca gaggaggtgc agcacattgt tctgatcatc      1020
     tgaagatcag ctattagaag agaaagatca gttaagtcct ttggacctga tcagcttgat      1080
     acaagaacta ctgatttcaa                                                  1100
//
ID   HSA_3558_IL2 standard; DNA; HUM; 1100 BP.
XX
AC   3558;
XX
DT   05-Sep-2005 (Created)
XX
DE   IL2: interleukin 2
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.4 123735159..123736258 (REVERSE)
CC   Score Points: 52 (100.0%)
CC   Chromosomal Location: 4q26-q27
XX
CC   Database Reference HGNC: 6001; IL2
CC   Database Reference ENTREZGENE: 3558
CC   Database Reference UNIGENE: Hs.89679
CC   Database Reference ENSEMBL: ENSG00000109471
CC   Database Reference REFSEQ: NP_000577
CC   Database Reference REFSEQ: NM_000586
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207849_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207849_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1538_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34021_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207849_at
CC   Database Reference TRANSFAC GENE: G000312; IL-2
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="4"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 123735159..123736258"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     702..724
FT                   /note="TRANSFAC Site R13412"
FT                   /note="TRANSFAC Site R13413"
FT   misc_signal     721..754
FT                   /note="TRANSFAC Site R00930"
FT   misc_signal     723..755
FT                   /note="TRANSFAC Site R09813"
FT   misc_signal     726..755
FT                   /note="TRANSFAC Site R00931"
FT                   /note="TRANSFAC Site R05035"
FT   misc_signal     755..773
FT                   /note="TRANSFAC Site R00932"
FT   prim_transcript 765..>765
FT                   /db_xref="ENSEMBL:ENST00000226730"
FT                   /note="Number of reported TSSs: 2"
FT   misc_signal     806..818
FT                   /note="TRANSFAC Site R00933"
FT   misc_signal     827..834
FT                   /note="TRANSFAC Site R00934"
FT   misc_signal     848..872
FT                   /note="TRANSFAC Site R03673"
FT   misc_signal     850..859
FT                   /note="TRANSFAC Site R00935"
FT   misc_signal     855..871
FT                   /note="TRANSFAC Site R03522"
FT   misc_signal     859..889
FT                   /note="TRANSFAC Site R04298"
FT   misc_signal     900..913
FT                   /note="TRANSFAC Site R02304"
FT   misc_signal     933..942
FT                   /note="TRANSFAC Site R00936"
FT   misc_signal     980..983
FT                   /note="TRANSFAC Site R00938"
FT   prim_transcript 1007..>1007
FT                   /db_xref="EPD:EP07114"
XX
SQ   Sequence 1100 BP; 384 A; 208 C; 165 G; 343 T; 0 other;
     acaaggactc tctctgagac aggatctcct caagtgtccc caggttaaat tagaagtata        60
     tatccgtaca attgttcagc cagtttgtgc actgtactga ggatgaatga acacctatcc       120
     taaatatcct agtcttctga ctaaaaacaa gatcatattt cataacgatt attgttacat       180
     tcatagtgtc ccaggtgatt tagaggataa ataaaaatcc attaaagagg taaagacata       240
     aaaacgagaa acatggactg gtttacacat aacacataca aagtctatta taaaactagc       300
     atcagtatcc ttgaatgcaa acctttttct gagtatttaa caatcgcacc ctttaaaaaa       360
     tgtacaatag acattaagag acttaaacag atatataatc attttaaatt aaaatagcgt       420
     taaacagtac ctcaagctca ataagcattt taagtattct aatcttagta tttctctagc       480
     tgacatgtaa gaagcaatct atcttattgt atgcaattag ctcattgtgt ggataaaaag       540
     gtaaaaccat tctgaaacag gaaaccaata cacttcctgt tttatcaaca aatctaaaca       600
     tttattcttt tcatctgttt actcttgctc ttgtccacca caatatgcta ttcacatgtt       660
     cagtgtagtt ttatgacaaa gaaaattttc tgagttactt ttgtatcccc acccccttaa       720
     agaaaggagg aaaaactgtt tcatacagaa ggcgttaatt gcatgaatta gagctatcac       780
     ctaagtgtgg gctaatgtaa caaagaggga tttcacctac atccattcag tcagtctttg       840
     ggggtttaaa gaaattccaa agagtcatca gaagaggaaa aatgaaggta atgttttttc       900
     agacaggtaa agtctttgaa aatatgtgta atatgtaaaa cattttgaca cccccataat       960
     atttttccag aattaacagt ataaattgca tctcttgttc aagagttccc tatcactctc      1020
     tttaatcact actcacagta acctcaactc ctgccacaat gtacaggatg caactcctgt      1080
     cttgcattgc actaagtctt                                                  1100
//
ID   HSA_356_FASLG standard; DNA; HUM; 1100 BP.
XX
AC   356;
XX
DT   07-Sep-2005 (Created)
XX
DE   FASLG: Fas ligand (TNF superfamily, member 6)
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.1 169358965..169360064 (FORWARD)
CC   Score Points: 3 (100.0%)
CC   Chromosomal Location: 1q23
XX
CC   Database Reference HGNC: 11936; FASLG
CC   Database Reference ENTREZGENE: 356
CC   Database Reference UNIGENE: Hs.2007
CC   Database Reference ENSEMBL: ENSG00000117560
CC   Database Reference REFSEQ: NM_000639
CC   Database Reference REFSEQ: NP_000630
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211333_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210865_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1851_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210865_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:210865_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211333_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:211333_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1858_at
CC   Database Reference TRANSFAC GENE: G001424; TNFSF6
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="1"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 169358965..169360064"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     138..159
FT                   /note="TRANSFAC Site R09922"
FT   misc_signal     236..272
FT                   /note="TRANSFAC Site R14704"
FT   misc_signal     750..773
FT                   /note="TRANSFAC Site R14693"
FT                   /note="TRANSFAC Site R14705"
FT   misc_signal     805..836
FT                   /note="TRANSFAC Site R14703"
FT   misc_feature    816
FT                   /note="SECONDARY ANCHOR: MMU [14103]; Alignment"
FT   prim_transcript 878..>878
FT                   /db_xref="ENSEMBL:ENST00000305730"
FT   misc_signal     894..906
FT                   /note="TRANSFAC Site R08191"
FT   misc_feature    947
FT                   /note="SECONDARY ANCHOR: RNO [25385]; Alignment"
FT   prim_transcript 977..>977
FT                   /db_xref="ENSEMBL:ENST00000340030"
XX
SQ   Sequence 1100 BP; 315 A; 228 C; 260 G; 297 T; 0 other;
     acttatgcct ataatcccag ctactcagga ggccaaggca agaggattgc ttgagcccag        60
     gagtttgagg ctgcagttaa ctacgatagc accactgcac tccagcctgg gtgacagagt       120
     gagactctgt ctctatttaa ataaataagt aaataaataa actgggcaaa caatgaaaat       180
     gaaaacattg cgaaatacaa agcagctctg tgggttccac tggtttgcag cctctgatct       240
     aatttctaaa gtgggtgtag caggttttta acctgtaaat tatggtgatc ggcaggtcag       300
     ggtaaatggt agttgtgtgt ggggaagaga tgatggcaac agatgttttc ctcctgcaaa       360
     aactaaaatg tgggagtgac ttctctggcc atgactccat ggtctctccc ctcagagcca       420
     ttttcagtaa aatttttata gtttaaaaaa tacggttctg aacaattttt gttagagtta       480
     ttttgggatt tttaaatagt tttttggttg tgtatatggt agaattctta aaattataca       540
     attataatgt ataaaaaagc atgcaattat aattcataaa attatagccc cactgaccat       600
     tctcctgtag ctgggagcag ttcacactaa cagggctata cccccatgct gacctgctct       660
     gcaggatccc aggaaggtga gcatagccta ctaacctgtt tgggtagcac agcgacagca       720
     actgaggcct tgaaggctgt tatcagaaaa ttgtgggcgg aaacttccag gggtttgctc       780
     tgagcttctt gaggcttctc agcttcagct gcaaagtgag tgggtgtttc tttgagaagc       840
     agaatcagag agagagagat agagaaagag aaagacagag gtgtttccct tagctatgga       900
     aactctataa gagagatcca gcttgcctcc tcttgagcag tcagcaacag ggtcccgtcc       960
     ttgacacctc agcctctaca ggactgagaa gaagtaaaac cgtttgctgg ggctggcctg      1020
     actcaccagc tgccatgcag cagcccttca attacccata tccccagatc tactgggtgg      1080
     acagcagtgc cagctctccc                                                  1100
//
ID   HSA_3562_IL3 standard; DNA; HUM; 1100 BP.
XX
AC   3562;
XX
DT   05-Sep-2005 (Created)
XX
DE   IL3: interleukin 3 (colony-stimulating factor, multiple)
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.5 131423246..131424345 (FORWARD)
CC   Score Points: 1 (100.0%)
CC   Chromosomal Location: 5q31.1
XX
CC   Database Reference HGNC: 6011; IL3
CC   Database Reference ENTREZGENE: 3562
CC   Database Reference UNIGENE: Hs.694
CC   Database Reference ENSEMBL: ENSG00000164399
CC   Database Reference REFSEQ: NM_000588
CC   Database Reference REFSEQ: NP_000579
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1263_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207906_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207906_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207906_at
CC   Database Reference TRANSFAC GENE: G000314; IL-3
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="5"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 131423246..131424345"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     701..707
FT                   /note="TRANSFAC Site R02734"
FT   misc_signal     743..751
FT                   /note="TRANSFAC Site R02735"
FT   misc_signal     847..862
FT                   /note="TRANSFAC Site R02736"
FT   misc_signal     857..875
FT                   /note="TRANSFAC Site R05026"
FT   misc_signal     876..893
FT                   /note="TRANSFAC Site R02682"
FT   misc_signal     887..897
FT                   /note="TRANSFAC Site R05027"
FT   misc_signal     926..953
FT                   /note="TRANSFAC Site R04907"
FT   misc_signal     949..954
FT                   /note="TRANSFAC Site R05028"
FT   prim_transcript 1001..>1001
FT                   /db_xref="ENSEMBL:ENST00000296870"
XX
SQ   Sequence 1100 BP; 240 A; 367 C; 270 G; 223 T; 0 other;
     tcacatcccc tctctgcaaa ccttgcctac tgggcctgca cctggcaaat ccatgctcag        60
     cacagacggg gatcaagacc tctcaataca actgtctcct gccaatccct gccccagcag       120
     cctgaggccc agtctgaaac cagggagttg ctctcctttc tcctcccttg acctcacccc       180
     tcagaccatg ccaattctgc ctcctaaacc tcccaggcca gcccctcccc cagctcccag       240
     tgacagtgtc ctcaggtacc tgagctcagc tctcggtgct accagaggga ctgccagggg       300
     ctgcagccgg gcctcctgca gaggctgagt cccacacgca gggaacagcc atgccactgc       360
     tagcagacca gtaagagaat ggccacctgg ggcctgagcg ccctcggcca tccaccagaa       420
     acaaagtgtc aaggagaagc tgcccgaagc ccatgggaca aaccactggg gactggaaca       480
     ccagtaattc tgtattggga agcggcacca agagatgtgc ttctcagagc ctgaggctga       540
     acgtggatgt ttagcagcgt gaccggctac cagacaaact ctcatctgtt ccagtggcct       600
     cctggccacc caccaggacc aagcagggcg ggcagcagag ggccagggta gtccaggtga       660
     tggcagatga gatcccactg ggcaggaggc ctcagtgagc tgagtcaggc ttccccttcc       720
     tgccacaggg gtcctctcac ctgctgccat gcttcccatc tctcatcctc cttgacaaga       780
     tgaagtgata ccgtttaagt aatctttttt cttgtttcac tgatcttgag tactagaaag       840
     tcatggatga ataattacgt ctgtggtttt ctatggaggt tccatgtcag ataaagatcc       900
     ttccgacgcc tgccccacac caccacctcc ccccgccttg cccggggttg tgggcacctt       960
     gctgctgcac atataaggcg ggaggctgtt gccaactctt cagagcccca cgaaggacca      1020
     gaacaagaca gagtgcctcc tgccgatcca aacatgagcc gcctgcccgt cctgctcctg      1080
     ctccaactcc tggtccgccc                                                  1100
//
ID   HSA_3565_IL4 standard; DNA; HUM; 1100 BP.
XX
AC   3565;
XX
DT   05-Sep-2005 (Created)
XX
DE   IL4: interleukin 4
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.5 132036571..132037670 (FORWARD)
CC   Score Points: 52 (100.0%)
CC   Chromosomal Location: 5q31.1
XX
CC   Database Reference HGNC: 6014; IL4
CC   Database Reference ENTREZGENE: 3565
CC   Database Reference UNIGENE: Hs.73917
CC   Database Reference ENSEMBL: ENSG00000113520
CC   Database Reference REFSEQ: NP_758858
CC   Database Reference REFSEQ: NM_000589
CC   Database Reference REFSEQ: NP_000580
CC   Database Reference REFSEQ: NM_172348
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207538_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1574_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207538_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207538_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207539_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207539_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207539_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33981_at
CC   Database Reference TRANSFAC GENE: G001214; IL-4
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="5"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 132036571..132037670"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     635..667
FT                   /note="TRANSFAC Site R14628"
FT   prim_transcript 702..>702
FT                   /db_xref="ENSEMBL:ENST00000231449"
FT                   /note="Number of reported TSSs: 2"
FT   misc_signal     759..791
FT                   /note="TRANSFAC Site R14631"
FT   misc_signal     806..838
FT                   /note="TRANSFAC Site R14630"
FT   misc_signal     840..852
FT                   /note="TRANSFAC Site R08171"
FT   misc_signal     922..946
FT                   /note="TRANSFAC Site R08170"
FT                   /note="TRANSFAC Site R13438"
FT   misc_signal     938..971
FT                   /note="TRANSFAC Site R14629"
FT   prim_transcript 1007..>1007
FT                   /db_xref="EPD:EP26038"
FT   misc_feature    1007
FT                   /note="SECONDARY ANCHOR: MMU [16189]; Alignment"
XX
SQ   Sequence 1100 BP; 309 A; 251 C; 238 G; 302 T; 0 other;
     atgtgtttag gttccattca aaaagtgggc attcctggcc aggcatggtg gctcacacct        60
     gtaatctcag agctttggga gactgaggta ggaggatcac ttgagcccag gaatttgaga       120
     tgagcctagg caacatagtg agactcttat ctctatcaaa aaataaaaat aaaaatgagc       180
     caggcatggt gcggtggcac gcacctactg ctaggggggc tgaggtggga ggatcacttg       240
     agcctgggag gttgaggctg cagtgatccc tgatcacaac attgcatttc agcctgggtg       300
     acagagtgag accctgtctc agaaaaaaaa aaaaaaaagt cattcctgaa acctcagaat       360
     agacctacct tgccaagggc ttccttatgg gtaaggacct tatggacctg ctgggaccca       420
     aactaggcct cacctgatac gacctgtcct tctcaaaaca cctaaacttg ggagaacatt       480
     gtcccccagt gctggggtag gagagtctgc ctgttattct gcctctatgc agagaaggag       540
     ccccagatca gcttttccat gacaggacag tttccaagat gccacctgta cttggaagaa       600
     gccaggttaa aatacttttc aagtaaaact ttcttgatat tactctatct ttccccagga       660
     ggactgcatt acaacaaatt cggacacctg tggcctctcc cttctatgca aagcaaaaag       720
     ccagcagcag ccccaagctg ataagattaa tctaaagagc aaattatggt gtaatttcct       780
     atgctgaaac tttgtagtta attttttaaa aaggtttcat tttcctattg gtctgatttc       840
     acaggaacat tttacctgtt tgtgaggcat tttttctcct ggaagagagg tgctgattgg       900
     ccccaagtga ctgacaatct ggtgtaacga aaatttccaa tgtaaactca ttttccctcg       960
     gtttcagcaa ttttaaatct atatatagag atatctttgt cagcattgca tcgttagctt      1020
     ctcctgataa actaattgcc tcacattgtc actgcaaatc gacacctatt aatgggtctc      1080
     acctcccaac tgcttccccc                                                  1100
//
ID   HSA_5468_PPARG standard; DNA; HUM; 1100 BP.
XX
AC   5468;
XX
DT   05-Sep-2005 (Created)
XX
DE   PPARG: peroxisome proliferative activated receptor, gamma
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.3 12304589..12305688 (FORWARD)
CC   Score Points: 1 (50.0%)
CC   Chromosomal Location: 3p25
XX
CC   Database Reference HGNC: 9236; PPARG
CC   Database Reference ENTREZGENE: 5468
CC   Database Reference UNIGENE: Hs.162646
CC   Database Reference ENSEMBL: ENSG00000132170
CC   Database Reference REFSEQ: NP_619726
CC   Database Reference REFSEQ: NM_138711
CC   Database Reference REFSEQ: NP_619725
CC   Database Reference REFSEQ: NM_138712
CC   Database Reference REFSEQ: NM_015869
CC   Database Reference REFSEQ: NP_005028
CC   Database Reference REFSEQ: NP_056953
CC   Database Reference REFSEQ: NM_005037
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:208510_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:208510_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:208510_s_at
CC   Database Reference TRANSFAC GENE: G004022; PPARG
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="3"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 12304589..12305688"
FT                   /note="Genomic Strand: FORWARD"
FT   prim_transcript 1001..>1001
FT                   /db_xref="ENSEMBL:ENST00000309576"
XX
SQ   Sequence 1100 BP; 173 A; 293 C; 450 G; 184 T; 0 other;
     gcgcggaggg ctggggccga gggtctgggg gctagggccg aggaaacggg aactgacggg        60
     gtcccagacg gatgagagct ggggagaagg gggtctcggc tgaggggtcc ggggctgagg       120
     cagggtcatg gtccggcagg acccggactg acgggtcgcg ggcgggcggc tcacgggtga       180
     ccgggtgaag gggtcttggg ctgagggcac ccgggctgag ggtcgcgtct accggagcgc       240
     gcactagggg cggagggcgc gggcacagag agccgcggcc ggtgccgact cgagtggacg       300
     cgagccggtg cgtcccggct tccaggacag cccccctcgg gagagcgccg ggtgggcgcg       360
     gagccgggga cacggggacc tccgcgtccc cggcggaggt gcgcaagcgt cgggagccgc       420
     tccgggggaa ctttggagca gggtgtctgg acccggggaa gcgaagatcc gcgtgcgtcc       480
     gtcctgaggc cgcgcggcac ccctgctgag gaggaggtcc cgttcgctgt ccagagccca       540
     ggggcgaccg ccgcttgggg accgggggac cgttcagcga ggggcgcgct tgtagctggc       600
     caggccctgt gccctgacgc gttgtgctgg ccctacgccc ggcggagggg ctggggacgg       660
     ggactgggtg cctccgtgcc tccgcggatg gagcgcgcag ccaggacccc cagccgcacc       720
     ccggggggct ggaaaggcga agtcgctgct ttgtgggctc ctgcaagtgc caggcgctga       780
     ccactcctcc tgggagccta actgaggggg gtagaggcag cagaggttaa cagaaatctc       840
     aggtcccttg gtggaaggtg ggtgtgtagt cgtggtactt tacgcctcgg tgtttaggga       900
     ggagcctaag gtaaggagtc agaaacgggg agtaaccgag ctgcggcttt tatataaggt       960
     cagtggtagg taaggaaggg gccttaacct ctgctggtga ccagaagcct gcatttctgc      1020
     attctgctta attccctttc cttaggtgag ttggctcact ctcattgcat tttgttggaa      1080
     tgtgttggtg ataggtccga                                                  1100
//
ID   HSA_5743_PTGS2 standard; DNA; HUM; 1100 BP.
XX
AC   5743;
XX
DT   06-Sep-2005 (Created)
XX
DE   PTGS2: prostaglandin-endoperoxide synthase 2 (prostaglandin G/H
DE   synthase and cyclooxygenase)
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.1 183381112..183382211 (REVERSE)
CC   Score Points: 7 (41.2%)
CC   Chromosomal Location: 1q25.2-q25.3
XX
CC   Database Reference HGNC: 9605; PTGS2
CC   Database Reference ENTREZGENE: 5743
CC   Database Reference UNIGENE: Hs.196384
CC   Database Reference ENSEMBL: ENSG00000073756
CC   Database Reference REFSEQ: NP_000954
CC   Database Reference REFSEQ: NM_000963
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1554997_a_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1069_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204748_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:204748_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204748_at
CC   Database Reference TRANSFAC GENE: G001237; PES2
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="1"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 183381112..183382211"
FT                   /note="Genomic Strand: REVERSE"
FT   misc_signal     859..883
FT                   /note="TRANSFAC Site R08091"
FT   misc_signal     882..912
FT                   /note="TRANSFAC Site R14626"
FT   misc_signal     917..941
FT                   /note="TRANSFAC Site R14627"
FT   misc_signal     930..956
FT                   /note="TRANSFAC Site R08092"
FT   prim_transcript 999..>999
FT                   /db_xref="ENSEMBL:ENST00000186982"
FT   prim_transcript 1000..>1000
FT                   /db_xref="dbTSS:SMR09283"
FT                   /note="Number of reported TSSs: 5"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: MMU [19225]; Alignment"
FT                   /note="PRIMARY ANCHOR: RNO [29527]; Alignment"
FT   prim_transcript 1007..>1007
FT                   /db_xref="dbTSS:SMR04184"
XX
SQ   Sequence 1100 BP; 295 A; 275 C; 278 G; 252 T; 0 other;
     ttaccagtat ctcctatgaa gggctagtaa ccaaaataat ccacgcatca gggagagaaa        60
     tgccttaagg catacgtttt ggacatttag cgtccctgca aattctggcc atcgccgctt       120
     cctttgtcca tcagaaggca ggaaacttta tattggtgac ccgtggagct cacattaact       180
     atttacaggg taactgctta ggaccagtat tatgaggaga atttaccttt cccgcctctc       240
     tttccaagaa acaaggaggg ggtgaaggta cggagaacag tatttcttct gttgaaagca       300
     acttagctac aaagataaat tacagctatg tacactgaag gtagctattt cattccacaa       360
     aataagagtt ttttaaaaag ctatgtatgt atgtgctgca tatagagcag atatacagcc       420
     tattaagcgt cgtcactaaa acataaaaca tgtcagcctt tcttaacctt actcgcccca       480
     gtctgtcccg acgtgacttc ctcgaccctc taaagacgta cagaccagac acggcggcgg       540
     cggcgggaga ggggattccc tgcgcccccg gacctcaggg ccgctcagat tcctggagag       600
     gaagccaagt gtccttctgc cctcccccgg tatcccatcc aaggcgatca gtccagaact       660
     ggctctcgga agcgctcggg caaagactgc gaagaagaaa agacatctgg cggaaacctg       720
     tgcgcctggg gcggtggaac tcggggagga gagggaggga tcagacagga gagtggggac       780
     taccccctct gctcccaaat tggggcagct tcctgggttt ccgattttct catttccgtg       840
     ggtaaaaaac cctgccccca ccgggcttac gcaatttttt taaggggaga ggagggaaaa       900
     atttgtgggg ggtacgaaaa ggcggaaaga aacagtcatt tcgtcacatg ggcttggttt       960
     tcagtcttat aaaaaggaag gttctctcgg ttagcgacca attgtcatac gacttgcagt      1020
     gagcgtcagg agcacgtcca ggaactcctc agcagcgcct ccttcagctc cacagccaga      1080
     cgccctcaga cagcaaagcc                                                  1100
//
ID   HSA_7124_TNF standard; DNA; HUM; 1100 BP.
XX
AC   7124;
XX
DT   07-Sep-2005 (Created)
XX
DE   TNF: tumor necrosis factor (TNF superfamily, member 2)
XX
OS   Homo sapiens (human)
XX
CC   Build HSA_May2004: Chr.6 31650317..31651416 (FORWARD)
CC   Score Points: 52 (100.0%)
CC   Chromosomal Location: 6p21.3
XX
CC   Database Reference HGNC: 11892; TNF
CC   Database Reference ENTREZGENE: 7124
CC   Database Reference UNIGENE: Hs.241570
CC   Database Reference ENSEMBL: ENSG00000111956
CC   Database Reference REFSEQ: NP_000585
CC   Database Reference REFSEQ: NM_000594
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1852_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U95Av2:259_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A:207113_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207113_s_at
CC   Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207113_s_at
CC   Database Reference TRANSFAC GENE: G000400; TNF-alpha
XX
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1100
FT                   /chromosome="6"
FT                   /organism="Homo sapiens (human)"
FT                   /note="Genomic Sequence Build: HSA_May2004"
FT                   /note="Genomic Positions: 31650317..31651416"
FT                   /note="Genomic Strand: FORWARD"
FT   misc_signal     103..128
FT                   /note="TRANSFAC Site R13135"
FT   misc_signal     103..130
FT                   /note="TRANSFAC Site R13135"
FT   misc_signal     479..494
FT                   /note="TRANSFAC Site R14424"
FT   misc_signal     815..827
FT                   /note="TRANSFAC Site R14422"
FT   misc_signal     827..841
FT                   /note="TRANSFAC Site R14423"
FT   misc_signal     829..851
FT                   /note="TRANSFAC Site R14632"
FT   misc_signal     841..858
FT                   /note="TRANSFAC Site R08185"
FT   misc_signal     876..919
FT                   /note="TRANSFAC Site R03186"
FT   misc_signal     880..894
FT                   /note="TRANSFAC Site R08186"
FT   misc_signal     881..893
FT                   /note="TRANSFAC Site R14625"
FT   misc_signal     889..909
FT                   /note="TRANSFAC Site R14470"
FT   misc_signal     897..914
FT                   /note="TRANSFAC Site R08187"
FT   misc_signal     913..925
FT                   /note="TRANSFAC Site R14624"
FT   misc_signal     917..934
FT                   /note="TRANSFAC Site R08188"
FT   misc_signal     923..932
FT                   /note="TRANSFAC Site R14623"
FT   misc_signal     941..957
FT                   /note="TRANSFAC Site R14708"
FT   misc_signal     941..975
FT                   /note="TRANSFAC Site R14622"
FT   prim_transcript 1001..>1001
FT                   /db_xref="EPD:EP11158"
FT   misc_feature    1001
FT                   /note="PRIMARY ANCHOR: RNO [24835]; Alignment"
FT   misc_feature    1005
FT                   /note="SECONDARY ANCHOR: MMU [21926]; Alignment"
FT   prim_transcript 1007..>1007
FT                   /db_xref="dbTSS:CCR05083"
FT   prim_transcript 1013..>1013
FT                   /db_xref="ENSEMBL:ENST00000229681"
XX
SQ   Sequence 1100 BP; 274 A; 322 C; 299 G; 205 T; 0 other;
     gggtcaggga gctcctggga gatatggcca catgtagcgg ctctgaggaa tgggttacag        60
     gagacctctg gggagatgtg accacagcaa tgggtaggag aatgtccagg gctatggaag       120
     tcgagtatgg ggaccccccc ttaacgaaga cagggccatg tagagggccc cagggagtga       180
     aagagcctcc aggacctcca ggtatggaat acaggggacg tttaagaaga tatggccaca       240
     cactggggcc ctgagaagtg agagcttcat gaaaaaaatc agggacccca gagttccttg       300
     gaagccaaga ctgaaaccag cattatgagt ctccgggtca gaatgaaaga agaaggcctg       360
     ccccagtggg gtctgtgaat tcccgggggt gatttcactc cccggggctg tcccaggctt       420
     gtccctgcta cccccaccca gcctttcctg aggcctcaag cctgccacca agcccccagc       480
     tccttctccc cgcagggacc caaacacagg cctcaggact caacacagct tttccctcca       540
     accccgtttt ctctccctca aggactcagc tttctgaagc ccctcccagt tctagttcta       600
     tctttttcct gcatcctgtc tggaagttag aaggaaacag accacagacc tggtccccaa       660
     aagaaatgga ggcaataggt tttgaggggc atggggacgg ggttcagcct ccagggtcct       720
     acacacaaat cagtcagtgg cccagaagac ccccctcgga atcggagcag ggaggatggg       780
     gagtgtgagg ggtatccttg atgcttgtgt gtccccaact ttccaaatcc ccgcccccgc       840
     gatggagaag aaaccgagac agaaggtgca gggcccacta ccgcttcctc cagatgagct       900
     catgggtttc tccaccaagg aagttttccg ctggttgaat gattctttcc ccgccctcct       960
     ctcgccccag ggacatataa aggcagttgt tggcacaccc agccagcaga cgctccctca      1020
     gcaaggacag cagaggacca gctaagaggg agagaagcaa ctacagaccc cccctgaaaa      1080
     caaccctcag acgccacatc                                                  1100
//