Tag | Content |
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EnhancerAtlas ID | HS061-18496 | Organism | Homo sapiens | Tissue/cell | GM12892 | Coordinate | chr4:917630-918980 | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 918356 | 918962 | chr4 | 918576 | 918805 | chr4 | 917889 | 918311 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I000921 | chr4 | 915595 | 919617 |
| Enhancer Sequence | ACATAAGACC TGTATCCAGA GTAAGCAGAA ACTCCCTGCC CAATAAAAAA TGGACAAAAA 60 GGCCAGGCGC CGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCAA GGCCGGCGGG 120 TGACCTGAGG TCAGGAGTTT GAGACCAGCC TGACCAACAT AGTGACACCC CATTTCTACT 180 AAAAAATACA AAATTAGCTG GGCATGGTGG TGCATGCCTT TAATCCCAGC TAGTTGGGAG 240 GCTGAGGCAG GAGAATTGTT TGAACCTGGG AGGTGGAGCT TGCCGTGAGC CAAGATGGAG 300 CCACTGCACT CCAGCCTGGG CAAGACTCCC TCTCAAAAAA AAAAAAAAAA AAAAATTGCT 360 GAACATCATC ATCAGGGAAA TTCCAATGAA ATCACAATGA GATCGACACC ACTGCACACT 420 CACAAGAATG GATGTAATCA AAATGAGAGA CCACAAGAAA TGCTGGTGAG GAAGTGGAGA 480 GCCAGGAACT CTCCACTGCA GCTGGTGGAA ATGTAAAATG GTGCAGCTAC CGTGGAAGGA 540 GGTTTGGTTG TTTCATGTGA AGTTCAACCT AAATCCAACC TGTAAATCAG CAATCCTACT 600 CCTTGGTATT TTTTACCCAA GACAAAGAAA AACACACGTC CACAAAAAGA CTTGAAAAAA 660 AATGTTCTCG GCACCTTTAT TCATAACAGC GGATACGGTT TGGATCTTTA TTCATAACAG 720 CGGACACGGT TTGGATCTTT ATTCATAACA GCACATACGG TTTGGATCTG CGTCCCCATG 780 CAAATCTCAT GTTCACTTGT GACCCTCAAT GTTGGAGGAG GGGCCTGGTG GGAGGTGACC 840 GGATTATGGG GCGGAGTTCC CCATGGCGTG GCTGCTCTCA GGATAGTGAG ATCTGACTGG 900 GCCATGGGTG TGGAGTTCCT CCCGGGGCTG CTCTCAGGAT AGTGAGTGCT CTCCTGTGAG 960 ATCTGATTGG GTCGTGGGGG TGGAGTTCCC CCGGGGGGCT GCTCTCAGGA TAGTGAGTGC 1020 TCTCCTGTGA GATCTGATTG GGTTGTGGTG GTGGAGTTCC CCCAGGGGCT GCTCTCAGGA 1080 TAGTGAGTGC TCTCCTGTGA GATCTGATTG GGTCATGGGG GTGGAGTTCT GCCCGGGGGC 1140 TGCTCTCAGG AGGAGGTTGC CAGGATCTGA GATCACACCC CTGTACTACA GCCTGGGCAA 1200 CACAACAAGA CTCTATCTCA AAAAAATAAG AATAAAAAAA TAACAGGCAC AGGATATGAA 1260 TGTGCAATGC CAGAAGGGGA GGCTGAGCAG CAAATAAGCA TTACCAAACT CGCTACTCAG 1320 AAAGGCACAA ATCAAAGCTT GACACTTTTT 1350
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