Tag | Content |
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EnhancerAtlas ID | HS091-09347 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:9260240-9261910 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr12:9261744-9261759 | AAAATAAAAATAGAA | + | 6.21 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 9261137 | 9261267 | chr12 | 9261323 | 9261373 |
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Enhancer Sequence | CTGTCATGAG AACATTCCCA AAGGAATCAG AGCAGACACT GAACCTCCCC ATTTTCTAGC 60 TATTTATATC TCCCCTTTAG CTACAGTATA TTCCCTGTCT GTACTTCCCT CTGCTCTCTG 120 CTGGGCTCAC ACAATATTGA AGACAAGAGT CACTAATGGC TCTTATAGAA ATCTCCATTG 180 CAACATGCTG AAATTTACAT TCTTCTTTTA TCATTTCTTT TTTTTCCTCG TTTTTTTTTA 240 GTTTTATCTT AAAAAAGTCT TTCTTATTAT AAAACTTAAA CCCGTTCTTA AAAGAGAAAC 300 AATACCAGCA AGACGAAACA AACAAAACAA AACAGAACAA AAAAAACCCA AACGCCCTCA 360 AGTCTACCTA GGAATACAAA CTATTAGTAC GATAGTGTCT CTTCTTCCAT CATCCTCTCC 420 CCATGTGCAG CCATCTCTAT ATCGAGTTTC ACTTGTTTAT TTTATTTTAT TTTATTTTAT 480 TTTATTTTAT TTTATTTTTG AGATGGAGTC TCGCTCTGTC GCCCAGGCTG GAGTGCAGTG 540 GTGCGATCTT GGCTCACTGC AACCTCCACC TCCTGGGTTC ATGCCATTCT CCTGCCTCAG 600 CTTCCCAAGT AGCTGGGACT ACAGGCGCTG GCCACCATGC CTGGCTAATT TTTTGTATTT 660 TTTAGTAGAG ACGGGGTTTC ACCATGTTAG CCAGGATGGT CTTGATCTCC TGACCTCGTG 720 ATCTGCCCAC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC CACGCCGGGC 780 CTGTTTACTT TTTTACAAAA GTGGGATTGT GTCGTAAATA TGTCATAGAC AATTGCTGGG 840 TTTCCAAGTG CATTTGTCTC CTTTCCTATT TGAGAATGTC CTCTGTATGT CTATTTGCAA 900 GATCACACCA GTTATGAGGA ACCAGGAACT TGGCCATCAC TGTGAGACAG AACTGGAGCA 960 GGGGCCTAGC TGAATAGTAG GTGTATTACA TGTGTGATCT TTGGACAGGA CTATACCTGC 1020 TCTTCCTGCT ACTGCTACTG TGTGCCACCA TGGATGGGAA CATAAGATCC AGGAAACAAG 1080 ACTTTTCAAG GTTGGAACAG ACTGTCTTGA GAAATCACGT TCAGTCTCTT CGTAAAAATG 1140 TCAGTGCAGA CAGGTATGTA GACCCGCCTT AGGTGGACTA GTGAGTTAGA TGAGATTTCA 1200 GTTGTATGCC TATCTCTACA AATTCTGAAT CTAAGTGATT TTTCCAGTAA GCATGCAAGG 1260 TCAGGTAAAT GATCTGTTGA TGATTGAATT TCCCCTATAG CCATGTGTTA ATTATCTCCC 1320 TAATATACGT TTGGTTATTT TTGGTTAAGG CAGAACCAAT ACCCTTCAAC ACTATCCACC 1380 CTTCCCATTT TGTGTGTGTG TGTGTGTGCA GTTTTGTCAC TTTCAGAATC AATCCTATTA 1440 GCATAACCTC TCTAGAAACA GTTTCTTACC TCATGATAGA ATAATACTGA TAAGAACGTG 1500 AAAGAAAATA AAAATAGAAA AGCAACAGGA GAATAACATT CTACAGATGA GGATGCTGTC 1560 AAAGCACTTA AAATTTTTGT GTTGCCACTG CTCCCGGAGA GAGTAGTTAA AATATCCCAA 1620 ATGGTGAGTC TCTTTTAAAT AATCCCCCAC AAAAGATTTT TAAAAAATGA 1670
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