| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12548 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:49092060-49092630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:49092315-49092334 | CGGCGCCCTCTGGCGGTCA | - | 7.08 | | ZNF263 | MA0528.1 | chr19:49092577-49092598 | AGGGGAGCAGGCGGGGGAGGA | + | 6.05 | | ZNF263 | MA0528.1 | chr19:49092565-49092586 | AGGGGAGGAGGGAGGGGAGCA | + | 6.56 | | ZNF263 | MA0528.1 | chr19:49092580-49092601 | GGAGCAGGCGGGGGAGGAAGA | + | 7.84 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27310 | chr19:49091844-49093429 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I048588 | chr19 | 49091858 | 49093070 |
|
Enhancer Sequence | TTTCAGGCAA GAGGGAAAAG CAGGTGCAAA GGCCCTGAGG TGGGTGTATC TGAGGTGCAA 60
GAGGGAGGTC GGTGTGGCCG GAGCCAAGTG AGCAAGTGGG GAAAGGAGTG GAGATGAGGT 120
CCGGGTGGGG AGGCAACAGG GGCCAAAATG TGCAGGGCCG CGTGGGCCCG GTGCGGACTT 180
GAGCTCTGAC CGAGTGACGA GGCAGCGCGG CAGGGATCGC AGCAGAGGAG GAGCCCGAGC 240
GGGCTTAGGC TTCACCGGCG CCCTCTGGCG GTCAGATGGG GACCGACTGT CGAGAGAGCA 300
GAAGCCGGGA AGCCCGAGAG GCGGCGCTGG CCGGGGTCCA GGGGAGGGGA CGGTGGCTGG 360
ACTAGGGTGA TGGTCACGGA GGTATTTTGA AGGTGAGACC GGGAGGATTT GCTGACAGAC 420
TGGATGTGGG TGTGAGAGAA GGGGATGAGT CAAGGGTGAC TCCAAGGTTT CGGCGGAAGC 480
AACTGTCAGG GTGGGGCAAC TGGGAAGGGG AGGAGGGAGG GGAGCAGGCG GGGGAGGAAG 540
ACACGGGCTC TGCGGCGGCC CATCCCACGT 570
|
