Tag | Content |
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EnhancerAtlas ID | HS187-22145 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr6:158676070-158677510 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I158256 | chr6 | 158677046 | 158677848 |
| Enhancer Sequence | TCCAGCCTGG GTGACAGAGT GAGACTCTGT CTCAAAAACA AAACAAAACA AAAGCAACAG 60 AAAAACTCTG TGTCCCTTGT CTTACTCCCT CACCCCCACC CTGTGGCCTC CCTCTGCATG 120 GATCCTGTCA TGTTTATGAA TCCCCCTGCA GGTGTTGCTG GAGGGGGCTT TCTCTTGGCA 180 GTTGTAGACA CTGTTGGGGA CCAGAGCATG TACCCTAAAT TGATAACCGG CAGACCCTGT 240 CGAGTGCATA TCTAATGTTC TTTCTTCCCT TCTTTCTAAG TAGAATTGGA ATTTTGTTTA 300 GAGAGCCTCT TGTCTCCTGT GTGACTCTGG GGAAGGTGAT CTTATCCCTA GCACTGGGGT 360 AAATCCTGAC TGGTTTCAGC TAGTCACATG GGTCCCATTC TCCGTAGGTG ATGACTGTAG 420 GGGTGAGCCA GAGACCTAGT TCTGGTCAGT GAGATTAGTG GGAGGTCTGT CCAGAGGTTC 480 TGGAAAACTC AGCCTTACAG CAACAACTCT AAGAATGGTG GCCTTTTCTT CCTCTGAAAG 540 TTGTCATGTC TGGGTGTGGT GCCTGGAACT GTTACAATTG TTTTGCTACT GGTCTGAGCA 600 TGAAGCCAAC ATCAGGTTAA GGACTGAGCC AAGCCAACAG CAGAGAGAAC TCTGCAGAGC 660 CCCAGTGCAC CATGCTTGGC ACCCACTAAC CTTGGACTTG TTCTGTGAAA TAAATTTTCT 720 TATTGTTTAC ACCAATTTAA GTTAGGGTTA TCTGTTATTT GCAACCGAAG ATGTGCTAAC 780 TGATGCAATA GCTGTCATTC TTTCCCTCAT TGCATGAAGA AGTACAGGGT ATAAAGGCAG 840 AATTGATCTA GTCAGAAGGT CAGAGGTGGC TTCCCTGGGG AAATGCAGAG GCCTTGGTGG 900 GAGAGATCCC TTTTCTTGCT GGGCCTCGTG TGCCACATTT AAGGATTTTG GTCTTTATCG 960 CAAGAGCAGA GCCTGTTATA GGTTTAAGTA CTGGGCTATG GCATGAATGC AGTGAACTCT 1020 TACTATTTAA AGTAACTCTC TAGTTACTTA AGCTACTCCT CCTGAAGAAC ACCTTGGCTT 1080 AACATTCCAG AGTTGAGTTT GATTTGCTGA GCAGGCAAGG AGCAGTCAGT GGTTAAGGCT 1140 TTGGTGATTA GTAGGTGTGT CCAGAAAGCA CAGAAGAGCA TCTTTGCTTG GAATCTGATG 1200 AAGTGAACAG CCCAGATTGT TTTCTTTTTT CTTTGCCAGT GCGTGCATGT GTGTATGTGT 1260 TTCTGTATGT ATGTATATAT ATAACTTCTG TGTGTGTGTG TATACGTGGT ATGTATACTA 1320 ACATGTACAC ACATATACCA CACTCACACA GGCAGCTTTC ATGTTTTCTA CTTTAAGGGT 1380 AACTTGTGAA CATCCTGTTG TTCTCTAAGT CTTTGATCAC TTCAATAAAA AAGTTGCAGC 1440
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