Tag | Content |
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EnhancerAtlas ID | HS091-00778 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:23289710-23291780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:23290864-23290883 | CACTGCCACCTTGTGGACA | - | 7 | Nr2f6(var.2) | MA0728.1 | chr1:23290648-23290663 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH01I022964 | chr1 | 23290781 | 23290970 |
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Enhancer Sequence | TGGAGGGAAC ATCACATGGT GAGGAGGGGA CAGAGATCAG GATAGGAATC TAGGGGGAAA 60 GTGGCAGCAA AGGCCAGAGC AGTGCCTCAA GGACAGCCCT CCCCAGCCGA GCCGAGCCGG 120 GGGATATCAG GGTCCAGAGA CCAGCCCTAG CCCCTGAGGG GCCTAGGGAG CAAAGTGTGC 180 CCTTGGGGAG GAGGCACAGC CCTGCAGGCC ACAGCTCCTG GTTGGTGGTC ACTGTACTCC 240 CCTCTCTCTT GCTTAACCAG CTTCCCATCT CCTGTGGTCA GTGGACTTAG ACCATTCTGG 300 CTGCGTGGGG CAGGCTCAGC CACATCTGTC TGTCTGACCT GCTGTCGTCC TGATTATGTG 360 TTTGGGTGGA CTTCGAGCCC CACTTAGGAC CCAGGCCTAA ACCACAGCGA CAACTCATTC 420 TCTCACCAGA GCTGAGCATC AGGGCTTTGG GGGCCTGAGT CTGTTCTGCC TTTGTCCGGG 480 TGTGTGGCTT CCTCGGCACC TCAGGCGAGA AGGTGAAGTG CTGGCAGGAC AGGATTCAGG 540 CTGTGATATC ATCACAGCAG CACCCAAGCC TCTTCCTCTA AGGCTGGAGT GGGGTGTGAA 600 GGGGGATGAG CATCCTCCAG GACTATTAAT ACATCCTCCT CGTCTTCCAC TGTGCCCTGA 660 GACTCCACCC CAAAACTGAG ACAAGGTCCC TGCGGTAGGT TTCATATGAC CATAAATTCT 720 TGAGACAGAG TCTCACCCTG TTGCCCAGGC TGGAGTACAA TGGTGCGATC TCAGCTCACT 780 GCGATCTCAG CTCACTTCAA CCTCTGCCTC CCGGGTTCAA GCGATTCTCC TGCCTCAGCC 840 TCCCGAGTAG CTGGGACTAC AGGCGTCCAC CACCACGCCC GGCTCATTTT TGTATTTTTA 900 GTAAAGCCAA GGTTTCACTA TGTTGGTCAG GCTAGTCTTG AACTCCTGAC CTCAGGTGAT 960 CCACCTGCCT CGGCCTCCCA AAGTGCTGAG ATTACAGGCA TGAGCCACCG TGCTCAGCCA 1020 TAAGACCATA AATTCTGTCA GCTCCTTCCA CCTTCGAAGC TGGCTGGCTT TGTGACTTGC 1080 TTTGGCCAAA AGAATGAGGC GGAACAAATT GCGACCTTTC TAGGCTAAAC CTTAAGGGGC 1140 TTACTCCCTG CGAACACTGC CACCTTGTGG ACAGGTCTGG GATAGCGGTC TTGAGAGCAG 1200 GAGTCCACGC TGAGGGAGAC ACCGCCCCCC TCAACCCGAC CCCCAAGCCG ACTTGCCCAG 1260 TGCACCAGAG AGAGCCCAAG CTAGACCAGC AGCAGAGCTG CCAGCCAGCC CACAGAATCA 1320 TGGGAAATAA TCACTTGCTT TGTCTGAAGC CAGTAGGCTT TGGGGTGGTT TGTTACTTAA 1380 CAATAGATAA CTGACGCAGA CCCAAACAGG AAAATTACAA ACCTTAGGGA GGATTTCTCA 1440 ACAACCCCAT GACATGGGTT TCACAGAATA GGGTGGTCCC AGCTAGAGCC TAGGCTTTGC 1500 TCAGCCTGGG ACCCAGGTAG GGGCTAGTGT CCACAGTGGT GCTCCTCCTG CTTTAATTGG 1560 CAAACAAAGG GCCTGGTAGT TATCACTGTC AGTGGTGGCT CCTTTATTGG GCCTTGACCC 1620 GTTCAGGAAG GAGAGGCTCC AAGGCTTGGC AGCTGCTGCC CCTGAACACC TGTGAGTTGT 1680 TCCTATTGAG GTCTTAGATA CAGCTGCAGG AAGGTCTTGA AAGGGGGCTG GAGCCTGGAG 1740 ATTCCATCAT GGTGGCCAAA GGCAGAGGAA GGGAAACACC GTTTGCTCTT CCTTTGGTGT 1800 CCTTGAATTT TACCCCCAAA CTGGGTGTCT TGAAGAAACC CCAGTGGCAT CAGGATCCTC 1860 ATTTTATACA CGAGGACATC GAGGCACAGA GAGGCAACAA GACTGTCCCA AAGATGCACA 1920 GCTAGTGAGA GCTGGACTCA GAATGGAGTC CAGAGCTTCT GAGTCTAAAT CTTATGGTCC 1980 TCCCCTACAC ACTAGAATCA GGGGTGGCAG CTCAAAGCCC AGGAGGACCC AGGGGGCTAT 2040 GGGGAGGAAC TCAAGGCTGT CTCTGCACTC 2070
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