Tag | Content |
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EnhancerAtlas ID | HS187-05017 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:118575270-118576530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 118576200 | 118576395 | chr11 | 118575800 | 118575951 | chr11 | 118575311 | 118575627 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I118704 | chr11 | 118575433 | 118576432 |
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Enhancer Sequence | ACTGAATAAA CATAAACATT TTAGTTTATT CCTTTTTTTC TTACAGACAG CGCTGGGGAG 60 AATGAACGCC TGAGTACTCA TGTCTTTATG CACTGTAGTA TTATTTCCTT ACAACAGACT 120 CCTGAACCTG GAACGGCAGT GTCAAAGGGT TCACAAAATG TTAGACTTCT GAAGCAAATC 180 AGATGGCACC TTTTTTGAAT AATGAAGAAT CTTTACCCCT GGCATGAGGA GCTGAGGACA 240 ACTCCCACTC CACGATGTGA AGCCACAGAG TTTCGAGGTA GTGGTTAATG GTGGTTGTGA 300 TTTTTTTGTT TTTGTTTTTG AGACAGAGTC TCTGTCACCC AGGCTGGGAG TGCAGTGGCA 360 CAATCTTGGC TCACCACAAC CTCTGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT 420 CCTGAGTAGC TGGGACAGGT GCCCGCCACC ATGCCTGGCT AATTTTTGTA TCTTTAGTAG 480 AGACGAGGTT TCACCATGTT TGCCAGGCTG GTCTCGAACT CCTGACCTCA GGTGATCCAC 540 CCGCCTTGGC CTCCCAAAGT GCTGGAATTA CAGGCGTTGA GCCACCACGC CCAGCTGGTT 600 GTGATGTTCT AATTTGGACT TGGAAGTCAA ATAATCGCCC CATGCCCTGT GGTTGCTGTG 660 GTTGCATGCC CTGCCCCGGT GGAAGCTGGG GAAGTGTTTC CTGTCTGTCA TCCCACCCAT 720 TCACGTGTCC TTATTATGGG TGAAGCCCAG AGAGCGAGAG CTCTCATTGT GGCCAAGGCT 780 GCAGCCTTGC CACTGTCACG GAGCACAGCT CACGTCTCCT CTGAGCCGTT ATTTTGTTTG 840 TATGAACCCA GAATGTATGT AAATTCTGAT GGGGTAAGCG GGCAGACAAA AAGGTCACTG 900 AAGTGTCCCA AACAGAATCT CATTGTGTAC TGGAGAGGAG GCAAAATAAT CACTTGCCAG 960 AGGGCGGAGC TTGGTTTTGT GGGACCTGAA GCTTAAATAA TTTGGGGAGG CCTCTTTAAG 1020 AAAAAGAATC AAATTATGAA TACAAAATTA GGATGAGGGT GTTTGAAGGG CCTCATGCAA 1080 GTGCGGTGCC TGGGACTTCA GCTTCATTAA CTTCGCGTTC AGTCTACGCC TGCTTGCCAG 1140 TGGACTGGGT TTGTCCTGCT TGGAGTCTGG TTTTGTTTGT TTCCAAACTT ATAAAATTAG 1200 ATGTCTTTTC TTCTTTCCTT TTGCATTTGC AAGTGTATTA ACATTTAAGA ATTGAGCAGG 1260
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