Tag | Content |
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EnhancerAtlas ID | HS091-45158 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr7:148923500-148925120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr7:148923532-148923549 | AGATCATGGAAAGGTCA | + | 6.57 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAGCATAT GCACGAAGTA TTTTCCTAAT CTAGATCATG GAAAGGTCAG AATGTCTTTT 60 GGTTGCAGGA GTGTGAGGAG AGGGGAGACG TCACTTGAGA CATGGGTTTA AAACACCTGG 120 CCGGGCGCGG TGGCTCACAC CTGTATTCCC AGCACTGGGA GGCCGAGGCG GACGGATCCC 180 GAGGTCAGGA ATTTGAGACC AGTCTGACGA AAATGGTGAA ATCCCGTCTC TACCAAAAAT 240 ACAAAAATCA GCCGGGCGTG GTGGCGGGTG TCTGTAATCC CAGCTACTCA GGAGGCTGAG 300 ACAGGAGAAT CGCTTGAACC CAGGAGGTGG AGATTGCAGT GAGCGGAGAT CGCACCACTG 360 CACTCCAGCC AGGGCGACAG AGCGAGACCC CGACTCAAAA ACAAAAAAAC ACCTGAGCAC 420 AAGGCTCAGT GTGATCCCTT TATTTTACCT TCAAGGGGCT GATTCCCAAG GAGACCTAGG 480 GACTGAGCTA GTGAGAGCCA AGCCTCTCTG CTTTCCTGTA TCCTAGGCTG GTGGATACCA 540 CTGCACCAAG TACCCCTCAG CTACACCATG AGTCGCCCCA AGCCCTGGCA CAGGTTGCTG 600 GAGCATCCCA TAGTGAGCCT CATCCCCAGA GCTGATCGGG GATGGTGACA CTCAGGATGT 660 TAGCCTCTGC TGGCTCCCAG GCAGCGAAGA TCCTCAGTGA AGACCCTGGA GTCCACATCC 720 TGAAGCAGAA CAGGGGTTTT GCTTTGGGGG TGGATTTTTA TTTTCCTTCT GAGAAAATGT 780 AGTTTATGTA GAGACAAAGT CTTGCTCTGC CATTCAGGCT GAGTGCAGTG GTGCAATCTT 840 GGCTTACTGC AGCCTTGACC TCTGGAGCTG AAGCAATCCG GTTGGGCGTG GTGGCTCATT 900 CATGTAACCC CAGCACTTTG GGAGGCTGAG GTGGGAGGAT TGCTTGAGAC CAGGAGTTTC 960 AGACTGCCCT TCCAACATAG TGAGACCCCT GTCTCTAGAG TAAAGAAAAA AATTTTAAAA 1020 ACAGAGACAG GCCAGGCATG GTGGCTCACA CCTGTAATCC CAGCGCTTTG GGAGGCCAAG 1080 GTGGATGGAT TGCCTGAGTT CAGGAGTTTG AGACCAGCCT GGGCAACATG GTGAAACCCC 1140 ATCTGTACTG AAATACAAAA AATTACCCGG CCGTGATAGT GGGTGCCTGT AATCCCAGCT 1200 ACTTGGGAGG CTGAGGCAGG AGAATCGCTT GAACCCGGGA GGCAAAGGTT GCAGTGAGCC 1260 GAAATGGCAC CACTGCACTC CAGCCTGGGC GACAGAGCGG GACTCCTCAA AAAAAGAGAG 1320 AGATAGGATT TCACTCTGTT GTCCAGGCTG AAGTGCAATG ATTCAATCAT TGCTCATTGC 1380 AGCCACGAAC TCCTGGGCTC AAGCAGTCTC TTGCCTCAGC CTCCCCAGTG GCTGGGACTA 1440 TAGGCATGCA TGCATCACCA CACCTGGCTA TTTTGTTTTT CTTTACTTTT TGTAGAGATA 1500 GGGTCTTGCT ATGTTGCCCA GGCTGGGCTT GAACTCCTGA GCTCAAGCAA CCCTCCCACC 1560 TCAGCCTCCC AAAGTGCTGA GATTACAGAT GTGAACTGCT GCACCTGGCC TTTTATTTAT 1620
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