Tag | Content |
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EnhancerAtlas ID | HS184-15590 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:43959440-43960280 |
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) |
Nr2f6(var.2) | MA0728.1 | chr19:43959449-43959464 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr19:43960180-43960201 | CTCTCTTCCCTTTCTTTCTCC | - | 6.06 | Zfx | MA0146.2 | chr19:43959474-43959488 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26835 | chr19:43959213-43960600 | Esophagus |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I043455 | chr19 | 43959468 | 43960352 |
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Enhancer Sequence | GGATGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCGGCCTCCC AAAGTGCTGG 60 GATTACAAGC GTGAACCACT GCACCTAGCT CATTTTATTT TTATAATGCC CATAAAGCAT 120 CAAACTGTGT GAGCACACCA TCATAAGCAT AACCAGTTCC CTCCTGATAA ACATTTAGGT 180 TATTCCTAAT GTTTTGTTAT TCCAAACACT ACTGCAATTA ACATCCTGGA GCAGACCTGA 240 CATCAGCCTC AGGCGTCCAT GTCTACATGT GAGATAAATT CCTGAGAGAA AAACCTGCCA 300 AGTCAGAAGC GATCTGCATT TGTCATTTAG AAAGACGTTT CCAAATTGCA CCCCAATTTC 360 CCTCCCCTGC AACTGATTGA CCAACCATTT CTCAAAAGGG CTTTTTGAGC ACTCTCTCTC 420 TCTCTCTCTC TTGCTGTCTC TGTATTTTTT TAATGTTTGA CAGCAAGAAG ATAGTCATGT 480 CTTGCTTATG TAATTAAAAT TAAACAAGCC CTTCGTTAAA AACACACAAA CCCAGGAAGA 540 AGAGAAACCA GCAAGGCCAG TTCAGGCAGA TCCACCCTGC CCCTTGTCAC ACCTGCCTTG 600 TCCCCAGCAA GCCCTGAAAA AGAGGCTGAA ATCAATTTCT CACACATGGA CCTCAGACAT 660 CAAACCTTGG AAAAAATACA GGAAAGAGAT TTTGTAACTT TCCCCCTCTG TGGCTTTTCG 720 TACGGCTAAA CCCTCTCACT CTCTCTTCCC TTTCTTTCTC CTCGTCCTTT TTCTTCTTTC 780 TCTCACTTCT GTTTTGGTGA GCTGTCATTA AAAACACTTT AAAGCCGTGT CCAGTCTAAT 840
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