Tag | Content |
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EnhancerAtlas ID | HS091-16698 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:21290280-21292440 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr16:21290635-21290646 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr16:21290636-21290646 | TCAAGGTCAT | + | 6.02 | MEF2C | MA0497.1 | chr16:21291720-21291735 | GAACTAAAAATAAAA | + | 6.07 | Nr5a2 | MA0505.1 | chr16:21290632-21290647 | TAGTTCAAGGTCATC | + | 6.87 | Sox3 | MA0514.1 | chr16:21291701-21291711 | CCTTTGTTTT | + | 6.02 |
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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 | CCTGAGATGG GGAAATAAAA TCGGAAAGGA ATGATGTAAA GCTTAAGGCA ATAAATCCTA 60 GTCATCAAAT CAGTGATAGG AAAAGTAAGT TAATTCAAAG AAAAGAGAGA TGATTTTGAC 120 CTGGAGTGGT TAGATAAGGG CTTCATGAAA GAGTGGGGAG AAACCAAGGT CTGAAATAAT 180 AATAGTGACG ACAACAATGA TAACATCAGG TTATTGATCT TTACTATGTA CCAGATACTG 240 CACCATGCAC TTTATGTATA TTATCTCATT TAATTATACA ACAACCTCTA AGGTAGGGAG 300 GTGTTGTTAT TAGTTTTACT GTCCATTGGA GGCTCTGAGA AGGGAAGAAA TTTAGTTCAA 360 GGTCATCCAC CAAGTCAGCA GAGGAGCTGG CTTTGCCCAT GGTTGGACTT CAGAATTATA 420 TTCCTAATCA TTAAGCTACT TTGGCAGAAA GAGAGGAAGA GGGCATTACA GGCCAAGTAA 480 AGCCCTGAGG TGGAAGGCAT GTTGAATAGC TCTGGGAACA GTGAGTTGCC AGATGTGTTA 540 GGCTGGAATA AGGTGCTGAG GTCTAGGAGC ATCAGAAGAT AAAACTGAGA ACGATTCTTG 600 GAGTCAGGCA GCTGAGAATG GTGATTCCTA GGAAAGAAAT TACATGCTCC AAGAGAGTAA 660 GCATTTAGAA AGATGGGTCT TCTGCCAATG CAAAGGATGG AACAGATGAG CGAGAGCAGA 720 GCCTGGGAGA AGGTCAAGAG GCAGGACTGC TGAAGTTGTG CTTTGTGGTA TTTTGGTTGG 780 AAGCTACATA GGGCATTTTG TAGGAAATGG TCACATCATG ATAAAAGACA GTGGATGAGT 840 AAGTGTCAAA ATCAGTACCA ATGAAATGAG AAATTGTACA TAATGTGTTT AGCAACAGTG 900 CTTGGCACAG AGTAGCCATG TAATAAGTGA ACACTGAGAG AGAAAGAGAG AGAGAGAGAA 960 GACACTGGTG GTTGGGAAAA GCTGATTTCA ATGACACAAT TTTGTTTCTT CGGTTCACCA 1020 TCCCTAGAAA TTTATGCCCA GAGCCGCTGG GCTTATAGAA ATGTTTCTGG CCCATCACGT 1080 GTGCTGTTAG CATTAATATT ACATCACATT TATTGGGTTT AGAAAGCACA GACATATAGC 1140 CCTGGCATGA TAGTTCACGC CTGTAATCCT AGCACTTTGG GAGGCCCAAG TGGGTGGATT 1200 ACCTGAGGTG AGGAGTTCGA GACCAGCCTG GCCAACATGG TAAAATCTTC TCTCTACTAA 1260 AAATACAAAA ATTAGCTGGG TGTGGTGGCG GGTGCCTGTA ATCCCAGCTA CCCAGGAGGC 1320 TGAGGCAGGA GAATTGCTGG AACCCGGGAG ATGGAGGCTG CAATGAGCCA AGATTGCACC 1380 ACTGCACTCC AGCCTGTGTG ACACAGTAAG ACTTTTTTGG CCCTTTGTTT TTGTGAATGT 1440 GAACTAAAAA TAAAATCCTA TGCCCCCCAC CTACTGAATG AACCCCCTCT GGGCCAAGCA 1500 GACCCCAGAA AAACCTTAAA GACTTAGTTT CCAGCCATGA TGGGATGGCA AATCAGATAT 1560 GCCTCATTAC ATCCTCTCCC TTTTAGAGTT TAGACACAAC TGAGCAGCCT TAATGTTAAT 1620 ACAGAGATCA CAAGACTGAC AGAACAGACT CTTTGTGGCA ATACGATAAC AAATTATAAA 1680 CAGGATCTAA GGCCATGCCA GGAAGGGTTA AGTCACGCAC CCTTACACTT AAAGAAAAAA 1740 GCTATGTTCT AACTGCCACA GAGTTTTTGT TTTCTCCAGC AGCTAAACAA GCACTGGCTT 1800 GAAGATAAGC AATATTTTTG TTTTTGTTTT CCCCAGCCCT GCTCAGAGAA GATAGGGAAC 1860 ATGGCTTGGG CACAGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCGGGC 1920 GGATCATGTG AGGTCAGGAG TTTGAGACCA GCCTGGCCAA CGTGATGAAA CCCCATCTCT 1980 ACAAAAAGTA CAAAAATTAG CCAGGTGTGG TAGCATGTGC CTGTAATCCC AGCTACTCAG 2040 GAGGCTGAGG CAGGAGAATT GCTTGAACCA GGGAGGTGGA GGTTGCAGTG AGCCGAGATC 2100 GTGCCACTGC ACTCCAGCCT GGACAACAGA GTGATTCTCT CTCTCTCTCA CTCTCTCTCT 2160
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