Tag | Content |
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EnhancerAtlas ID | HS002-07397 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr4:55451900-55453550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr4:55451942-55451953 | TGTGACTCATT | + | 6.62 | FOSL1 | MA0477.1 | chr4:55452623-55452634 | CATGAGTCACC | - | 6.62 | Gata4 | MA0482.1 | chr4:55451960-55451971 | AGGAGATAAGA | - | 6.14 | JUND | MA0491.1 | chr4:55452623-55452634 | CATGAGTCACC | - | 6.02 | NKX2-5 | MA0063.2 | chr4:55452552-55452562 | ACCACTTGAG | + | 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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| Number: 1 | ID | Chromosome | Start | End |
GH04I054585 | chr4 | 55451900 | 55453279 |
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Enhancer Sequence | CTCATGCTGA AATTAGCTAC CAAGAAACAT CACTAGGACT CCTGTGACTC ATTACTGTTG 60 AGGAGATAAG AATGTGGGCT TTGGAGTCAT CAAGACAGAG TTGGAAATTC AGCTCCACCA 120 CTAAATGTGG CTCTTCATGC AAACTACTGC ACCTCTCTAA GCCTCGATTC TTCATTCATG 180 AAATGAGAAT GATGTGTGTG TAGTTCCTAA CAGACTGTTA GCAGTAGCGG ATTCTTACAG 240 GTCTGCAGCA ACCTGGATTC TTGCCTCAAG TTTTGTTGAG AGGTTGTGTG GTTGATTTCT 300 GACCTTCTTA AATTATAAGT ACAGGTATAT AAAATGTAGG CTAGCTACAG CATAGCCAAA 360 GCCCAGGAGC TGATTAATTA GCCTCAGTTG ACCCAGCAAA TAGCCTTGAT AGAGTTTTCA 420 TTTAGGCTTG TTGATAGCAC TGCAAGAGGC TATTCATCAG AAGCGTGTCA ATCCTGATAC 480 TTGGTTGCAT TGGTTCCAGT GCTGGAGACA AGAAAGCTGA TCAACATGGG TTTCATAGAT 540 TCAACAAGGT GGTCTCTGGT GTTTTCCTTT CCTTGGTCAC ATTGCAGTTC CAGTTCCTAT 600 TGAGAAGGGT CTGAATGCTG TCCTTTCCTG CTCTCTGCCT TGCTGTTTGC TTACCACTTG 660 AGAAGCGATG GGAGCTAGTG CTGTGACCTC CAGCTCTTTG CAATGTAATT GAGTCTATAA 720 AACCATGAGT CACCAGGACC ACATGAGCTA CAGAAAGCTC ACACAGTCCA AGTATATAAA 780 ATGTAGACTA ACTAAAGCAT AGCCAAAGGC AAGTCTTAGA GCAGGAGTGA AAGTTCGTTA 840 AAAAGTATTA GAGCAGGAAT GAAAGGAAGT AAAGTATGCT TGGAAGAGGG CCAAGCAGGA 900 GACCTGAGAA ATCAAAGTGC CCTGTTTGAC TTTTGACTTG GGGTTTCATA CGTTGGCATG 960 CTTCTGGGGT GTTGCATCCG TTCTCCCTTG ATTCTTCCCT TGGGGTGGGC TGTCTCCATG 1020 TGCAGTGGCC TGCCAGTACT TGGGAGGAGC CACATGTGCA GTGTGTTTAC TGAAATTGTG 1080 TACATGCTCA CTTGAGGCAT TCTTCCTTTA TCAGTCAAGT GTTTCTAGAG GAAGGTCATA 1140 TACCAGTTAA ACTCCACCAT TTTGCCTCTT AGTGTACATG CTCAAGCCCA CTCGCCCAAC 1200 TCCTGAGATC CTATCAGGAA GCTTCTGATC ACTAACTTTC GGTGTTTTCT ATTTACTGGG 1260 AGACTGCATT TCCCTGGCAC TGGCTGTGAC CAATTGTTAT TTTAGAGAGA TAGTTTTGAC 1320 AGCCACCTGA CCATCACATG ATGGTTATCT GACATTCCTG GGATCGGGGC ACCTCTCCTA 1380 CCCTGTGCAT ATTTGCCTTA CTATCTATTG TAATAAGATC ATAATATAAT CGCAGTAATT 1440 ATTAGGATGT TTATTATTCC AGGGAAATTT GTATTTATTC AAGCCTCCTG AGGACAAACA 1500 GCCAGAAGAG TCACAAAAGC AAGGATTTCC CTGACTTTGC AAATTGCCCT ACATAGAAAG 1560 CCACTCCCAG CCTGGCTTTA GTATGCATAT TTTGAGAGCC CAGTTTATTG ATGTATAATC 1620 ACTCCATATA GGTGGGTAGG AAGTTGGTTT 1650
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