Tag | Content |
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EnhancerAtlas ID | HS040-02416 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:153478860-153480020 |
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 | GTCTTTAGGA AACCATATCA CCTGGATCCA ACCTCTGGGT TCCAAATTCA ATTTCTTCTC 60 AGCTACAAAA TCCTTCTTGC TACATCACCC CTGTACGCAC AGCCACATGG CACCCAGGTC 120 CACATGGGCA GTGAGCCACC ACCTCTCATC TGCTTCCTCT GTCACAGGAC TACAAGGGGC 180 TGAGCAAGGT AGGCATGGTC AGGGTGCCAG GCATCAAGGG ACAGGGCTAT CGGATCAGCC 240 GGGCCTGTGC TGTGACAGGT AGGAGTGAGG CAGTATGATT GGGAGCACCA CCAGCACCAC 300 TAAAAATGGG GAGAGAAAGT TCCGCTAGGA ATGGGGTTAT CAGAAATGGG AAGAGACGGT 360 GGTCAGACCT GTGTGGGTGA AAATGAATGC AGGAATGACA CCAAAGACCG GCTAGCTTCC 420 ACAGCCCTTT GCAGGATGCT CTGAACTTGC TGAGCCCTTT CACACCCGCC ACCTGGTCCC 480 TGTTGACCCA CCAGCTGTAT GCAGCTGACT ATCTTCACCA GCTCCTTGAA CAAGAATTTC 540 CATTTCCAAG GCCAGGGTGG GGGAGGCTGC AACATTTTTT GCCAGAGAAT CCAAAGAGCA 600 CATGAGTCAG CTGCCTGGGT CAAGGCCCAG ATCCCTGTGG CGGGTCAGCC AGAGAGCAGG 660 AGCTGGCCCT GAAGAGGGGA AGGGGGAAGA AAGAAACCCA GAGGGCTCAG AGAGCACAGG 720 ACCCTGCCCA CGTGGGCCAC TCTGCAGAGG CCAGGCCCAA GGCTGAGTTG GGCCTCCCAC 780 ACAGACATGG AATGAGAAGG CTGTCAGTGC AGGACAGGGT GAGGACACAC TCAGCGGGCA 840 CGGCTTTCTC CCCTAACAGC CACTCCACCC AGGGGCCAGA AACTGACTTC ACCTCTGCAC 900 TGAATTCCTC CCCCCATGTC TCCCTCCTCC CACCCATCTT CCTCCTGGTG CTTCCAGCAG 960 AGCCAAGAAG GCTTCGCCCC ACCTACTCCC CTCCTGCTGA CACGGACCCC CCACACACAC 1020 ACCCAAGGAA CAGGAATACC AAAAATGATA CTACCAGAGT GAAGCGTGTC CTGCAGACAT 1080 TATCTCTTTA ATCCTAACTA TAATAGTCCC TATTTCAGAG ATGAGGCAAA TGTGAGAGAA 1140 CAAGTAACTT TCCCAAGAAC 1160
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