| Tag | Content |
|---|
EnhancerAtlas ID | HS052-09942 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr12:124425700-124427290 | | | 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 |
| GH12I123941 | chr12 | 124425866 | 124428205 |
| Enhancer Sequence | ACACGGGTAG CTCCTTTCCC AAGGCTTCAG TGCTGGCAGG TGTGGACGCT GGAGGTCCCT 60
AGTGTCAGGC TGAAATCCTG TTCCTCTGCA TTCCCACAGG CCCAGCTCCC AGTCCCAGGG 120
CTTCGGGGGA GGTCCCTGGT ATCCCTCCAC AGGGAGACTT CTGAGGACAG GCTCCCATTC 180
CACCACCCCA AGAAGCCCAC GGCGCCTTCC CTACCACACG CAGACAAAAA GATGTCTGGG 240
CTCCTGGGTG GCGCACTCAG GAGGCTGTAA TATGAGCAAT GCAAATGGAA AAAAATCAGT 300
GCTCGGTAAT CCACTAAGGC TTGGTGGAAA TGGTCTGTGT CTTTTACAAG GAACTGGACA 360
CTCTCATGAA TAGTAACTGC CATTGTGAGG CCTGTTTAGA AAAAGGCATT GTGGGGAATG 420
GAGAAGTTCT TCAAAGTTTC TTGAAACCAT AAAGAGCTTG TCATTTCCTT GCTCTATGTA 480
TATCTCTATA TATGTTCCAG TGTAGCTGCT CCGCCTTGCC CCGGCACGCC TGCGCAGGGC 540
TGAGCGAGCC CTGGACCATA GTGCATGCTC TTCCTTATTT GGAAACTCTC CTGACCCTCT 600
CATGACTAGC TTCCTCTTTT CTTTGTCCTC TTTCCCTTTT GCCTATTTAG GAAAGTTTCA 660
AGCTGTTAGC CAATCGGGTC AAGCTTAGAA TGTGAGGTCC CATTCCAGTC AATGGAAACT 720
GGACACAGTC ATAGGGCAAT TGCATCAGGT TATGAAGATT ATAAATGTCC TCGTCTCCTT 780
TGTTTGAGTG TGCTCTCGTG GTAAGACTGC TGGCGAGTTG CACCCTTTCT GCAGAAAGTA 840
AACTAGCCTT GCTGAGCCAT CCATTGCCTT CCCGACGTGA TAAACCCGTT TCCAACAGGT 900
GTCTCTGCAC AAACATGGAT TCAGCACTTT CCAAACACCC ACCCTGTTTT AGGGAGCAGG 960
CTCTTTGCAG CAGGCACAGA GGGCCCTGGG AAGGCCTGGG TTTCTGTCTC TTCTCTGGCG 1020
GCCAGCAGGC AGCTGCCCTT TGGGGTTTCC TGAGGTCCTG GAGGATTCTG GTTTGGGGAG 1080
GGTTCTGGGG CTGTAGTCCA GAGAAAGCCC CAGATCCTCA GGGAGCTGTC TAGTAATGTG 1140
ACCACTCGCC CGCCAGCATT TAGCAAGCTG CTGCTCTGTG CCAGGCCCAT GCTAGGCGGC 1200
AGCGACACGG AGGAGCGGGG GCGGTTCTGC CCAATGCTGC TGCTGCTGTT ACTCCTCCTT 1260
TTGGGTTTAA CTCACGTCTA TTTTTATGTC CTGATTACAC AAGGAACACA TGTTCATTGT 1320
AGGAAAATCA GAAAAACATA TAATAGGCAT TCCAAATATA TGTGTCATTC AAAAGAAAAC 1380
AAAATCACTC ATCCCCCTGC CCACTAATAA CCACTTGCAA CACGGAGGGA TCCAAACATC 1440
CTTCTCATCT TCTCTTAGAG AGCTCAGGCC ACACGCATAA CTCTTCCCAG CAAGAGCATT 1500
TTCTCCTAAG TGTGTGACTA GTGAAAACGG CACCAACACG TACCACAAAG GGAAACCTAC 1560
TGTCATTTAC TTCTGGGGAG GAGTTCTTAC 1590
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