Tag | Content |
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EnhancerAtlas ID | HS176-38623 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:131286800-131288230 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr7:131286856-131286871 | AGGTCAGAGAGACCT | + | 6.44 | NFYB | MA0502.1 | chr7:131287250-131287265 | CTGATTGGCTCAGGT | - | 6.87 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_32786 | chr7:131286677-131288403 | H1 | SE_55996 | chr7:131287062-131288353 | u87 | SE_68730 | chr7:131286207-131288383 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I131602 | chr7 | 131287140 | 131293439 |
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Enhancer Sequence | CTCAGGCACA TAAAGGAACT TCAGCTTCTT TGGGAGAGAC AGTGGGGGTG GAGGAAAGGT 60 CAGAGAGACC TTGAGGCTTC TACAGTTCGG CATGTCGCCT CGCCATAATT TGGGGTATCA 120 GTTTCTGAGC CCCCAAAATG CAAGAAGGTG TTTCAGGAAC CCATCCAGGC ACCATTTAAC 180 AGGATTTATC AGTAACCCAA TGTGTCCTGT GGCACCTGCT AGGTAGGGGT GCAGAGAAGC 240 ACTGTGACAG AGCCTGGGGC TGTACAGCCT TGTACCTGCA GCTTCTCATT CTGGGGAGAG 300 GACTGAGCCT CCTCTGCTTT GCGGCCTCAT AGCTCCATCC CTCCCGTCCC TGCTTGCCTT 360 CCAGGGCCAT TCTCTGCTTT TCTTCCAGGG CCATTCTGCT TCTCTGCCAA CCACCACATG 420 GGTCCCCCTG GGCATTGGCT GCAGGAGAAC CTGATTGGCT CAGGTAATCA CCAGCTCTTG 480 GACACTGGCC AACCAATAGA GCGGCAGCAT CCAGGTCAGG TGCCCACCCT TGGTCCAATC 540 AGCTGTGGCC CAACTGCCGT AGGGCCCATG GTGCAGGTGG TGTTTTTAAA GGGGGCTGCA 600 GGTGAGCCAG GTCTTGCGGT GTCAACTACA CGAAAAAAGC GACCCTTTCA GAAGAATTCT 660 AATGAGAGAG CCATGTCGTC TACCCGGGAC GTGTGATTGA ATTTTTGTGG TGCGATGGGG 720 TATGGGATAA AATCTCTCTT GTGTCATCCT GTGGAGACTT GGTGAAAGGC TCATCACCCA 780 CACATCCTCC TGGCATTGGA CTTGTGTTTT GGAGGGAGTT TGGCTGTGCT GACTCAGGCT 840 TCCCGGGAAG GCACAGGTTT AGAAAAGAGG CTGCTCCTGG GGGCCAAGCC ACCACTGGTT 900 ACCTACAGAA AAACTTGAAA TTTGGCAGTG AATGGAAAGG GAAAGTGGGC TGACTCTATT 960 GGAGTAACAG GAGCATCTGT GTACAGACGC AGAGAGACCT GTGCGGATGG AGAGACAAAC 1020 ACGCCAACAC ATGCCTAGAC AAACAGTGCG GGGCAGAGAG AGAGGCTCTG AGAGCCACAG 1080 AGAGCCACAT GCAGGGAGAT AAGCACAGAG CCAGAGAGAT AGAGACTCAG ACACAGAGAT 1140 AAACACTCAT ATGAAGCAAC ACACCCAGTG GCACACTCAT TCACCCAAGC AAGCAGAGGG 1200 CTGTAGGGAG CTTGCAGCTC AAGTGGAGCC AGGCTACTGG AAGTGAACAT TGCATTGTCC 1260 CTTGATGTGG GAAGCTGAAG CCGTCTACTA CAAAAAGGAA AAGGCCATTT TCCCAAAGAT 1320 CAGGATTTCA TTGTAAAGGA GTTGCTGGGC TCATCTCAAG AAAGGAGGGG CTGACACAAG 1380 TCAATATAAT CCATTTTCAG AGGAAACTGT GTTTTCTAAA TTTGAATCAG 1430
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