Tag | Content |
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EnhancerAtlas ID | HS116-02087 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:153478840-153480020 |
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) |
ZNF263 | MA0528.1 | chr1:153479529-153479550 | TGAAGAGGGGAAGGGGGAAGA | + | 6.03 | ZNF263 | MA0528.1 | chr1:153479781-153479802 | CCCTCCTCCCACCCATCTTCC | - | 6.16 | ZNF263 | MA0528.1 | chr1:153479784-153479805 | TCCTCCCACCCATCTTCCTCC | - | 6.53 | ZNF263 | MA0528.1 | chr1:153479769-153479790 | CCCCCCATGTCTCCCTCCTCC | - | 6.86 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_02992 | chr1:153478832-153481149 | Bladder | SE_28418 | chr1:153478695-153480927 | Fetal_Intestine | SE_36529 | chr1:153479156-153480743 | HMEC | SE_52579 | chr1:153478743-153481142 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I153506 | chr1 | 153478735 | 153481271 |
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Enhancer Sequence | TATCACATGG TCTCTAAACT GTCTTTAGGA AACCATATCA CCTGGATCCA ACCTCTGGGT 60 TCCAAATTCA ATTTCTTCTC AGCTACAAAA TCCTTCTTGC TACATCACCC CTGTACGCAC 120 AGCCACATGG CACCCAGGTC CACATGGGCA GTGAGCCACC ACCTCTCATC TGCTTCCTCT 180 GTCACAGGAC TACAAGGGGC TGAGCAAGGT AGGCATGGTC AGGGTGCCAG GCATCAAGGG 240 ACAGGGCTAT CGGATCAGCC GGGCCTGTGC TGTGACAGGT AGGAGTGAGG CAGTATGATT 300 GGGAGCACCA CCAGCACCAC TAAAAATGGG GAGAGAAAGT TCCGCTAGGA ATGGGGTTAT 360 CAGAAATGGG AAGAGACGGT GGTCAGACCT GTGTGGGTGA AAATGAATGC AGGAATGACA 420 CCAAAGACCG GCTAGCTTCC ACAGCCCTTT GCAGGATGCT CTGAACTTGC TGAGCCCTTT 480 CACACCCGCC ACCTGGTCCC TGTTGACCCA CCAGCTGTAT GCAGCTGACT ATCTTCACCA 540 GCTCCTTGAA CAAGAATTTC CATTTCCAAG GCCAGGGTGG GGGAGGCTGC AACATTTTTT 600 GCCAGAGAAT CCAAAGAGCA CATGAGTCAG CTGCCTGGGT CAAGGCCCAG ATCCCTGTGG 660 CGGGTCAGCC AGAGAGCAGG AGCTGGCCCT GAAGAGGGGA AGGGGGAAGA AAGAAACCCA 720 GAGGGCTCAG AGAGCACAGG ACCCTGCCCA CGTGGGCCAC TCTGCAGAGG CCAGGCCCAA 780 GGCTGAGTTG GGCCTCCCAC ACAGACATGG AATGAGAAGG CTGTCAGTGC AGGACAGGGT 840 GAGGACACAC TCAGCGGGCA CGGCTTTCTC CCCTAACAGC CACTCCACCC AGGGGCCAGA 900 AACTGACTTC ACCTCTGCAC TGAATTCCTC CCCCCATGTC TCCCTCCTCC CACCCATCTT 960 CCTCCTGGTG CTTCCAGCAG AGCCAAGAAG GCTTCGCCCC ACCTACTCCC CTCCTGCTGA 1020 CACGGACCCC CCACACACAC ACCCAAGGAA CAGGAATACC AAAAATGATA CTACCAGAGT 1080 GAAGCGTGTC CTGCAGACAT TATCTCTTTA ATCCTAACTA TAATAGTCCC TATTTCAGAG 1140 ATGAGGCAAA TGTGAGAGAA CAAGTAACTT TCCCAAGAAC 1180
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