Tag | Content |
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EnhancerAtlas ID | HS116-17533 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:2849670-2851440 |
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) |
POU2F2 | MA0507.1 | chr2:2851060-2851073 | TACATTTGCATAT | + | 7.12 | ZNF263 | MA0528.1 | chr2:2851195-2851216 | GAAGGAAGTAGAGAAGGGAGA | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33649 | chr2:2847186-2856385 | H2171 | SE_66981 | chr2:2847186-2856385 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I002846 | chr2 | 2849874 | 2851350 |
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Enhancer Sequence | GCCCTCCTCT CTGACAGGAT CCTTCCCTGG GAGGTTTTCT CTCAACTTCT ACACCCAGAA 60 CTGTCTCCAA AACGGGAAGC GTGTTAGCTG GAAACGACTC GTTCCTAGCA AGGCTGCTCC 120 ATCTGCATGG GCTCGGCGCT GCTGGGATCT GGGATCCGTC CTGACTTGTG ATTCTGGTGC 180 TGTTGCCTTG GGATCCTCGC TGAAATGCCA GCCACTACGT TGGCTCCCTT ATAATCACCT 240 CTTGCCCACT AGGGAAGGTA AAATAGCATC GAATCAGGAG GAGGAGGCAT CGGAAGCACT 300 GTGATGGGGA CGTGGTTAGG TTTTCTTCCT CCAGCCCTGA ACAGGAGCCT CTGAATTTTT 360 CAACAGCTGT CTTTGCCCCT CTTGGAGAAA GCCCCGTCTG TTCCCCCTTC CTCACTGCGT 420 AATCCTTCCC ATACGCCCCT GCTCGCTGCC ATTTCTGAAG GACACAGGGG GCTTCTGTTA 480 CCTGAGCCCT TTTTCCCTCA CAGATGCCTG CAGGCTGAGG CTTGCTGGGG AGGCCTCTTC 540 AAGGGACGCC TAGCCCCTGG ACATCATCCA AGTTGGCAGC TTCACCACAG AGCTGCTGAG 600 AGAAAGGCGC GGGGGGCAGC CTGGGCTGGC CTGCTGAGCC AAGATAAAGC TGCAGGAACC 660 TGCTGCTGCC AGAAGGGATG TTTGCTGGGT TCCCACAGGT GACCAATGCA GGCAGAGACC 720 AGCCAGGACT CCAGCTCAGG GACAGTGATG GGCACAGGGT CACGCAGGGC TCTAGGCTTG 780 GCCCAGGTTT TGAGCCAACA ACACCAGCTG CCTGGTGGTG GGAACAGACA CAAGCACCAG 840 GCTCAGTTTT CAAAGCTCTC CTCCTCCTTC TCCTGTTATT TAAGGTCATA CCACATTGGA 900 AGTGAGTCAG GCAGGTGGAG CCCTTTATGT CCATGAGGCA GGTGCAGCAG CCCAGGGAGG 960 CAGGGTGGCC TTTCCCAGGA ATAGCCAGCG TCACCTGGAG GCAGAGCCAG GCGAGGGCTG 1020 TGTGGGTGGC TCCCAGCCAT GTGGACAGCA GGCCTGACTG TCCCTGTCCC CATGAGCCTC 1080 ATGAAGGTGC CGCGGATCCG TCCAGGCGTG GGTGTTGTTC TCTTCCGGCC CAGCCTTCTC 1140 CCTCTTTCCA CACACACGAT TGGGCCAGCA TCTCCCGTCT GCTGCCATCT CCTCTGCTGG 1200 TGGGGGTGCG TCAGCTGACC CTGTGCCCTC TGGCCTCATT TTTCATGGGT GTTGCCACTG 1260 TCTGGCTGTC TGCCCCTTCC CACATTAACT CTCACCCTCT GGCGGCAGAG ACCTTGTCTT 1320 GCCCATCTCT GTATCTCCAG CCCCCAGTGG CCCTCAGTGC GCATTTGCCA AGGGAAATAT 1380 ATGCAAAAAG TACATTTGCA TATCACAGCC CTGTGAGGCA GACACACCCA GAATCATTGC 1440 TCCTGCTTTG CAGAGAGGGT CTGTCCCTGG ACCCCGTCTT TGACTGCTGG GGCCTGAGGG 1500 TGTGGGCGGA CAATGAGGCA CATCAGAAGG AAGTAGAGAA GGGAGAGTGA GAGCCTGTCT 1560 TTCGTCCAGC TCCCTCCCTG CAGGGCCACC CCTGGCCAGC CTTAGACCAA AGGACACAGA 1620 TGCCAGCAAA TGTCTCTGCC AGCCCCCGGG GCTGGCAGGT GGCCTCCCTC CCAGCCACAC 1680 TCAGATGCCA TGGCTGTGAT TACAAAGAAC ACAGGGACCA GGGCACTTGG GCTCTGTGTG 1740 ACAACCCTGT GCAGCTGGGG ACACACACAC 1770
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