Tag | Content |
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EnhancerAtlas ID | HS091-33478 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:50989830-50992350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr22:50990785-50990796 | AATGTATCAAT | + | 6.62 | PLAG1 | MA0163.1 | chr22:50990841-50990855 | GAGGCCAAGGGGGG | + | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | ACTGCAACAA GCAGACAGGA CTGGTCAGGC CACAGGGAGG GGCTGCAGCT CTGGGGTGCC 60 CCAGAAGGGT CAGATGCCTC CAGCTGGGCT CAGCATCTGG AGGCCCAGAT CCTGCTGAGG 120 CACCCAATTA CTCTAGGGAG AGACAGCTGG TAGGCTACTT GTTACAGGCT CATAAAAACT 180 CCCTACAAAC ATCCATAGTG ACGCTTCCTA GTCTCATGCA AGGCATAACT TCTGGATACA 240 CCAGACATGA TGTAAAAAAC TAGAGGCTGG TCTGATACGA AATGTGAGGA GAATTAGAGC 300 AAACCGCAGC TCCTTACCTA CAAGCAGTTC ACAGCCAATG GCTGCAGGTG ACCCCTAAGG 360 AGTCATCCAC CCAAGCTCAC ACACTCAGGT AGAGTTGATT GTTTCCAGTC CTGCAAGACC 420 CAAACCTCAT GTCACCTTAT GTTCAGTGGC CTGGGATGCC TGCCCACCTC CACCTGGGCA 480 CCTCTATGCT TTCGTTGAGG CCCAGGCCTG GGGCTTCTCC TCTTGGGAAG GTGTCCTTGA 540 CCATCTACCA ATGCACTGAT GGGCTCTCTT GCTCTTTCCC TCTGACAGCA ACTCGAAGGT 600 AGCATTCCCT GGGCCTATAG GTGAACACAT GCTTCTTGTG TGAACTCAAA GAAGTGTGTG 660 CAGAAATCCC ACCTCCAACT TTTTCTCTGC ATAGTCCACC GGCTGGTGTG GTTCAGCCCT 720 CTGCAACTAT ACAGAACAAA GGTCATCTCC CCTCTGCATG ACAACCAACT GTACATAGCA 780 AACACATCCC CTTAAAATTC CTCTTTGTGG AATCCTCACA AGCATCCCAG ATCGTTCCGG 840 TGCAGGGAGG CCGCAGACTA CCTGGACAGC AGGTGCAGCA GGGACCTGGG GCCAGAGCAG 900 AGTACGCCTC CCAGCTCCCC ACCTGACGAC TCTGTGACCT GGAACAAGTG TCTGCAATGT 960 ATCAATCTCG GCCGGGTGCG GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCAAG 1020 GGGGGTAGAT CACGAGATCA AGAGATTGAG ACCATCCTGG CCAACATGGC CAGTGTTCCT 1080 GGCCCATCTC TACTAAAAAT ATAAAAATTA GCCGGGTGTG GTGGTGGGTG CCTGTAGTCC 1140 CAGCTACTAG AGAGGCTGAG GCAGGAGAAT CGCTTGAACC CAGAAGGTGG AGGTTATATA 1200 TACATAAATC TCAGTCTCCT CATCTTTGGA GACCCTACCA ATCTCATGGC TTACTGTGAG 1260 AATTAAATGG GTGATATATG TAAACTGCCT GGCACACATG TTATGGACTG AATGTGTCCC 1320 TCCCACATTC ACCTGTTGAA ATCCTAACCC CCGACGTGAT GGTATTAGGA GGTCGGGTCT 1380 TTTGGAGATG ATTAGGTCCT AAGGGTAGAC CCTCCTGAAT GGGATTAGCA CCCCTTAAAG 1440 AAGAGACACA AGAGCTCACT CTCACTCTAT GCAAGGATAT GTGAGGCTCT ATGTGAGGAT 1500 ACAAGAAGGT GGCTGGCCGG GCAAGGTGGC TGGTACCTAT AATCCCAGCA CTTTGGGAGG 1560 CTGAGGTGGG TGGATCACTT GAGCTCAGAA GTTTGAGATC AGACTGGGCA ACATGTTGAA 1620 ACCCTGTCTT TACAGAAAAT ACAAAATTTA GCTGGGCATG GTGGTGTGCA CCTGTAGTTG 1680 CAACTACTCA GGAGGCTGAG ATGAAAAAAA GGATCCCTTG AGCCTGGGAG GTGGAGGTTG 1740 CAGTGAGCCA AGATTGCACT ACTGCACTCC AGTTTGGGTG ACAGAGTATG ACCCTGTCTC 1800 AAAATAAATA AATAAATAAA TAAAATCCCA AAGTGCTGGG ATTACAGGCC ACTGCGCCCA 1860 GCCATAACGT TTTTTTGAGT GCAAATTAAA TCATTGTTTC TTGGCTACAA TAATCCTCTA 1920 GAGAGGACCA GATTGTAACT TTTCCTCATA TTTTTCGTTG GTGCCCTAAT GGAATAGGTT 1980 CCTTTTTCTG TTCTAATGCA CAAATTACTC TTATAATTGT CAAACTTATC TCCCCTCATT 2040 TTGCTTCCAA GGAAACTAAA ATCATGGTAT TCTGCAGATG ACCAAAGATA TGAATCTCCC 2100 TCATTTGGCA TCGCACTGGG CCCGGATCTG TTACACTGCA AATGCCCTGC TGCTAAAACG 2160 ATACAAACAC CCTCCCTCTA TGCCCAGGGA CTATCACAGA AGAGAGAGTC TCGCTCCGTC 2220 ACCCAGGCTG CAGTGCAATG GTATGATCTC GGCTCACTGC AAGTTCCGTC TCCTGGGTTC 2280 AAGTGATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGATT CCAGGCATCC ACCAACACGC 2340 CCAGCTAATT TTTGTATTTT TATTAGAGAT GGAGTTTCAC CATATTGCCC AGGCTGGTCT 2400 CAAACTCCTG ACCTTGTGAT CCTCCTGCCT CGGCTTCCCA AAGTGCTGGG TTTACAGGTG 2460 TGAGCCACCG TGCCCAGCCT GTAGCAGATT TATATAAAAA TGCAATATGC GGCTGGGTGC 2520
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