Tag | Content |
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EnhancerAtlas ID | HS139-30021 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr2:127982420-127983700 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 127982512 | 127982840 | chr2 | 127982879 | 127983060 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I127224 | chr2 | 127982503 | 127985235 |
| Enhancer Sequence | GAAAACACTG TCCATTTATT TGTTCCTTTC CCTTCCAGCG TGCAAGAAAA ACGGAAGTGA 60 GATTCCAACA GGAGGGCACC ACTGTCCCTG TCTGACCTTA AACCAGGAGA TTTTGTACAG 120 ATGTATTCCT TCAAGAAAAC CAGCTTGTTG GCAGTAATAG AGAAGAAATG AGCTTCTCCC 180 AACAACAGCC AACAACAGCC AATGACAACA GCAAAATAGG AAAAAGGGTT GCCCTCTGAA 240 AGGTAAATAA ACTCTATACA CAATAAATGA CCATCTGTGG AAGTAAAACC GAGAGACAGG 300 CTTTACCACC TCCCAGAACT CCAATCCAGA TGACCACGGA TAAATCTCTA GCACGCGGAA 360 TAGAGATGTC ACGGCTGTTA GGTAAGCAGA GAGTAATGCA GGGTATATAT TCCTGGAAGA 420 GAACAGGGTT AGTCAAACTG GATCTCAGAA AAGGGAGCTG CTGTACAAGA CATTCTAGGA 480 AGCAAGCCTC TGAATTCTGA AACCCAGACC TGCTGGTCAC GGTGGGGCAG GGATGATCTT 540 CCAAGCTTCC CTGCGGTCTG CATGAAATTC TCTCACCCAC ACCAGCTTCC TGTGCTCCAA 600 TTCCATGCCT CTGACTGGTT TCCACTTAAG AATTAATGGG TAAAAAGGAA AAAGAATTAG 660 TAGTATGATC TTGTTGCTTC CCCAGAGTCA TCAATAAAAA GGCAGAACAG AGAGAAAACA 720 AAACAAAACA AAGTTATACC AGGAGACAGA ACTGGGAGAT CTCAGATCGT CTTCTCTGTG 780 AATCGGGTGT TGCTACTGAA GCCGTGATAA TCCTGGTCAC CTGAGGCAGA AAATAAACAT 840 TTCTTCCTAC AAAGAATGTG GGCATTTTCC AGTGGGATTT GTGAGCCAGC AAAGACTTAG 900 CAGCAGTTTC TTCACTGCCA AAAATCTCTA ACTTTCCATG ATGAAAAACT ATTGTTGTCA 960 TTGACCGGCT TTACGAAATA TTGGCTTACG TTTTAATCAT CTGTTGAGCA TCAGGCACTA 1020 TCCTGGGCAC CTGTGAATCC ATTTGGTCCT CGCAGCTATT CTATGACATG GGCACATTAT 1080 CCTCCTTCAC AGATGAAGAA ACAAGTTAAA GAGATGTTCC CAAAAGAGTT AAGTTAGGAG 1140 CAAAGTTAAT ACTTGAACCC AAATCTGTTT CCAGGGTTTT TATGCCTTTC ACTACACCTG 1200 CTTTGCAGGA AAGTGATGAG AATTTCTAGT AGACGCTGAG TAGGGGCGGT GCTGCACGGC 1260 ACTCACTGTT TCTGAGATAC 1280
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