Tag | Content |
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EnhancerAtlas ID | HS091-12353 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr14:21163680-21166750 | SNPs | Number: 3 | 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 |
GH14I020697 | chr14 | 21165760 | 21166292 |
| Enhancer Sequence | ATCTACAGAC TCAGTGGTTA GCTTCCTGTT AACTAATTTC TGTTGACAGG TACTTGGATA 60 TTTTATTTAG AAAGTGGTTG CCAATAAATT AGTTATAAGT CGCCAGTTTC ACTGCCTTGT 120 GAACACATAA TTATTGTGGT CTCAGTATTC CCTATGGTGG CTTCTCCTGC TCCTGGTATT 180 GCCCTGAAAT GGGCCAAAAG CCGTGGCTCC CCAATACTCA GGTTATAGAA CATTGTCCAG 240 GTACCACCTA GGAGAGCCCA GCCTCACTGA AAGTATTCAA ATTTAGGAAT GGGTTTGAGA 300 AGTAGGTAGC TGGTATGTGC TTAGCACAAG AATCTCTCTT CCTTGGGTTA GTCTGTTTCA 360 AAACTGAAAA CACTGTCATT CCTTAAGAAA ATAGGAAAAA GTATTCCAAA CCTCTGTCAC 420 TAGAAAATTT GCCATATTAC CAAATCTCAA AAACCTCTCA GGAAATGAGA AAGTCCCAGT 480 TTCTGGTAAA CTATTTGGGC CCTTTTCTCA AGTTCTCCAA CCAGTGCTAT TTCCTTGAGG 540 TGAGGCAAAG TTACTCAAGA TCATCGCTGC CACTCAAGGC CTTGATAGGG CAAGTGAAAG 600 GCATGGACCA TTATTATATT GATCACAGCA TAAGCTGTGA AAACCCACAT CTTCTCCAAA 660 CATCTGCTTG GAGCATTATC ATCGCATAGT TTGCTCTGGT GTTCAGGGAA ATCGCTGTTT 720 CATAGGAAAT CACATGGCAG TGGGATGGGA GTGTTTCCTG ACCTGCCGAT GGTACTGGCA 780 CCTGAGCAAG CATTCCTAGT CCTTTTTGGT CTGGGCCTCT TGTTCTATCA CAACCACAAG 840 CTGTTTAAAA TAAAACGTCA AGTCACAGGC AGGTCATTTT ATCCTGCGTG AATCAATTGA 900 AGAATTGAAG TCCTGGTCAG CTGTGATTGT TGGCTTTGCA AGGAAAAAGA AGGAACACTC 960 CAAAATGCTA AATGCTTTGA AGAATAGTGA CATGCAAGGA AGAAAATTCC ATGCAATTTG 1020 GAGAAGAAAC ATTTTTCTAG GAATCTAGTA GCTGAGATAT TTTATAGTTT AAAAACAGAC 1080 TTCCAATATC TTGAGAATAC AGTTAGCTCT ACGAAATAAA GAGGAGTCAA TAATATATGC 1140 AACTCTGTAG TCATTCATTA TTTTATCCAG ATTGACAGAA GCAGAGGAAA CCAAGAAAAA 1200 TGGAAGTGGT AAAAAAAAAA AAATGCAGTA ATTGCCAATA TTTACTGAGC ATTTACCCTG 1260 TGCTAGGCCT TGTTATAGGC GCTTAGATTG ATTTTCTTTT CATAACATCC CTAAGAGGTA 1320 GGTATTACAT GCTCATTTTG CTTATGAGGA AATCTGCTGA GAGAGATTAA GTAATTTTCT 1380 CATGGTCACA GCCTCAGTCT TTTAGACCAC GGTGTCAAAA GAAGTTCTTA CTGTGAGTCA 1440 GGGTGGTGCA GTGGAGAAAG CGTTTGGGGA AAATCCTGAC CCAAAAGTGT GCGTTGGGAT 1500 GATGTGGAGA TCATTCAATT TTCTCTTGTA GCTACAGCTT TGAGATGCAC CCATTGGTAT 1560 CCACACTGGC CTGCTGTCCT CAAATATTTC TCTATGTCTT GTTTACTTGA GTAGTGCAGA 1620 AAAGCTGACG TCCTGGGTCT GCTCTCGCAT GCATAGGTGA GGTTTTCTCT GTAGCTAGTC 1680 ATCTTGCTAA ACCATATTTT TGGTCACAAA GAATCAGGAT GAGAGAAAGT AGATAAAACC 1740 ATGGAAACTC GAGGTGCCAC CGGAAGAGCA AACCAAAGTA TATTGATCTG CTGAAGCTAT 1800 AATCCAAGTA CTAAGTATAC CTTCAGAAGT TGTATGCATT GTTCTTGGGG CAAAAAGGAA 1860 ATCAAACATC TGCCCTTCCT CCCACAACCT CTTTACTTCC CTCTCTTCCT AACACTGTAT 1920 CTCACATCTA CAGCTGCAGG CACACAGATA TGACATACAG CTTGATATCT TTATGTGCAA 1980 AGGCAAAAGA TGGCTATGGA TATAGGAGGT GGCATTTAAA AGAACAATAT CCATGTTTGA 2040 TACTGCTTTC ATTATCAATA ATGAAAAGGT AGCCTTTCAG CAGAACAAAG TAAGGTACAG 2100 GTCGTTTGGA AGCCATTTCA GTCATTCACA CAGTGTGATC CACCATTACG AAGCAGAATT 2160 TGAAATCAAA AGACAATAGT ACCCATATAC ATCAAACTAG GAGTTCAACT GGGGTCAGTC 2220 CTTGGACTGC ACATACAGAG TTGGGCTGCC TGACTCTCAA AACATTGCCC TTGCTAATTT 2280 GCGTTGCTCA CTTCCTATTG AATCAGGGAT GATTTTTCTT TGCTGTAGTG AATCAGCCCT 2340 GCTACACTGC AAGAATCAAG CCGATTCACA ATTCACATCA ATTCCAGGAG TGACGGCCAG 2400 ATGGCAGCAT CTGGCTAGTC AGTTGGTGAG TGAGTCCACC TCCAGTCTTG ATTAAACTCT 2460 GCTGCTGGGA AGTAGCAATT CTGAGCATAA ATGTCTTTGA TATCCTGAAT ATTTTGGGTG 2520 TGGGATGAGA GAGGCAGTAG ATAGTGGAAA GAGCACAGGG TGTAGACTAA GATAGGCCTG 2580 GATTCCTTTC TTTAATCTGT CAATGAAAGC AATGAATGTT CTGAAACTAC ATGGCAATGC 2640 TTTTTTTGTT GCCACTCTGG CTTTTTTTTT TAATGCTATA AAATATATGC CTATTTTTCA 2700 CTGCCAAGAG GTGACAACAC AATGATGCTG CAACCAGAGA AGACAGACAG CTACCAACAA 2760 CTATTGACAA GACAGAAGGA ACATCAAGAA TAGATGCAAG ACAAAGCAAT GTATCTCCAT 2820 GGCCTAGATT TTTTAGGTTA TGCATAGAAA CAGCAAGGAG AAGAAGACAC AATCCAAGTT 2880 TTCTTTTGAG AATATTGTGC TGTTTAAATT TATTTTTTAA ACATTTCTTA GCTTTTCTTA 2940 TTAGTCAATT TCATAAGCCT GGGAAACATC TTTACTCTAT CCATTTAATT GCATTTGTTC 3000 ATTAGCTTAC TCATTTCACT TATTAGTTCA TTCAAACAGT AGCTATTATC AACTGTCTTC 3060 TAAGAACTGT 3070
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