Tag | Content |
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EnhancerAtlas ID | HS091-30560 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:31885400-31887700 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr20:31887101-31887120 | CACCGCCACCTGGCGGCCA | - | 7.29 | Klf12 | MA0742.1 | chr20:31886335-31886350 | GGCCACGCCCTCCCG | + | 6.05 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH20I033299 | chr20 | 31887021 | 31887190 |
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Enhancer Sequence | GCTCTGCTCT CTCTCCCACT TTTTCCTTTA CTACGGAGCT GGCCTCCAGA CCCTGACTCC 60 ACCAAGGGAA GGCCTCCCCA AGTCAGGCCT GAGCTGCAAC TCAGGCCCAG AAGCAGGTGA 120 GACAAGCATC AGTTGATCCC TGCCCCAGAC GCGCAGACAG AAATTCGCCA CGACTAGGAC 180 TTCATGAGCT CTTACTATTT GTGCAGTTGT CAGGTCAGTG GATGCCCCAA GTTCAAATCC 240 CAGCTCTGCC CCTGACTTGC TCCATGACTT TGGGAAAGCT AATTTACCTC CTCATCCTCG 300 GTTTCCTCAT CCATAAAATG GGGCTTAACC ATCCCTACAA CATAGGATTG TTAGTGAGGA 360 ATAAAAGTCT ACAGGAAAGT TCTGGGCACA TAGCAGGTGT CCCTCTTGGC ACAGAGAAGC 420 ACTTACAAAT GCATGCTAAA TGGATGGATG GATAGATGGA TGGATGGATG GATGGACAGA 480 CAGAAGATGC TAAGATTACA AGCATGAGCC ATCACACGCA GCCCCCGGAC TAGTTTTTAT 540 GGATACTTTA GAAAACTGCA GCATCAAATA GTTCTATCCA TCTCGTTGCA GTTTCAAATT 600 TTCCCTCCAT CCAAAGGGTT TGAGGTATCT GAGAAATTAA AGCATGGGTT AAAAACTGAG 660 ATATCTGGTT TAAAAAATAA AAATCAGAGA TGATTCGAAG GGCAAAGACG GAAGGAAGTC 720 ATTTCTCCCT CCCCCAGCAT AGCAGATACG GGAGGGCACA GGCTCCTGCC CCCACATCAG 780 AACTCTGCCA TGCTCAGGCC CCCAGAGTGG AAACTGGCGG AGAAGAAGAA AAGTCTACCA 840 ACTGCACTTT GGGATCAGAA GAGGCTCATT CCAAGGGCGA CCAGAGAGGA GAAGGGAGAG 900 CAGCATGCAC TGAGCGCCAC AGGGCATCTG CCATGGGCCA CGCCCTCCCG CTGGGTGTTT 960 TGTATAGGCA CATCTCACTG ACTCCTCAGA CAACTCCATG AGGTGGCAGT CATGACCCCC 1020 CTTCACTGTG ATGAAAGAGG CTCCGAGCAA TGAAGTCACT GTCCAAGTTC ACAGAGGCAG 1080 TTGGTGATAG AGGAAGACTT GAGTTCTGAG CGAGTGTCAT TCGGATTGAG CCGTTACTAG 1140 GTGCCAGTTG TATACATGAA GCAGGAATTA CTATTCTACC GCCGTTTCTT TCCTTTTTTC 1200 TTTTTTTTTT TTTTAATTCC CAAAGAGTTC TTCCAATCGT CAGATATTTG GTCAGTATTC 1260 AGAGTAGGAT CCAGAGTTCA CACATTACAT TTTGTTGACA AGTCTGTAGA TTTCTCTTTG 1320 TAAATCACAT TTTTTTGTTG TTGTTATAGC CATTTTCGGG GACCTTATTG ACTTTAATAT 1380 ACTTTTTTTT TTTTTTTGGA GACGGACCTT TTTTCTTTTT TTAAAGTAAT TTTTACAGGA 1440 GTCATGCTCA TCGTCTCTAT GTCCTTCCGA TTTTAGTACA TGTGCTGCCC TGGCGGGCAC 1500 TATACCCTCA TTTTAAGACG AGGAAACAGA TTCAGACGCG AGAAGAGACC AGCCAAGGTC 1560 ACTGGGGCTC AAACCGAAGT CCAGCTGGCT CCTCCGCTGC CCCGAGGACG GGCCCGGAGG 1620 TCTCCCTGGA GCGGTAGGCG GCCGGTCCCT GGCCCTCCAG CACTCCCCAT CCTCGGCCAT 1680 ACACCGGGGC AGGTGACACA CCACCGCCAC CTGGCGGCCA AGTGGGGAAT TCTGACGCGA 1740 ACACGAGATC TTTGGGGGGA GCAGAGGAGC CAGTTTGGAT TTCAGAGTAG ATGTTACCAG 1800 GCCTCTGGCT TCCAGCCTAA GCTTCCTTGA GATCCAGGTG CTCATAGGGT GTCCAGACCC 1860 AGAACCACCT GCATGGGGGA CGCGGCTTTC AGTCTGGTAG GGGCGGTGGA GTGTTACATA 1920 CAATAGTTCA GTTCCGTTCC AAACCGGGAC TTTGGCATAA AACCGACTGG GTTCCCATGC 1980 TCTCATAGTA TGGCTTTGAA CAGGTCATTT CCCTTTCCTC AGACTTGGTT TCACCATCTG 2040 TAAAAGGGGG TAATAATAAG ACCTACTTCC TAACGTTATC ATGCAGATGA ACCAGCTGAC 2100 ATGCAGAGGC CTGGCACTTA GTGGATGCTC GATAAATGTC ACTGTCATCA CTGTTTGCAT 2160 CATTATTATC AACATCATTA TTACCTGCTC CTCCCTACCT GCCCCCCCAT GCAACAGTAC 2220 AGCTCCACCT GGAAGCAGCC CCCCAACTTC CCCCTCCAAT ACTGCCCTCC ACCCTCACAG 2280 AACTTTCTTC TTGTCCTTGA 2300
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