| Tag | Content |
|---|
EnhancerAtlas ID | HS197-13605 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr21:38090700-38092120 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr21:38091109-38091122 | TTCTAGAACATTC | + | 7.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26793 | chr21:38089754-38092580 | Esophagus | | SE_32017 | chr21:38090453-38092619 | Gastric |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I036718 | chr21 | 38090908 | 38092610 |
|
Enhancer Sequence | TGTTGTCTCT CCTCTGATGG AGAGCCACAG GCTCCCAGCG ACACCTGCAG CAAGACACAC 60
CTAAAAATAA CAAGGGGGTG GCTCGGGACA AGACACACCA TGAGCCTCCT TTTGTTATCT 120
TGAGTTACCC TCTCTCCTTC CGGCAGGGTC AAGAAGGAAT TCTCCAGACC TACCCAAGAT 180
CCTTCGCCAC CCAAGGACGG TTTCCCACAT GCTTTGAGTT TCTTCTCAGG CTGGGCACTG 240
GGACTCCCCT TGGTGGTGGA GGAAGTCCTA CCACTGCCCC TGGGCCTCCC CTGAACAATG 300
CTGGGGTTCA CCGACTCACT GTCCTTGTCT GCCACCCTCA GCACTATTGA TTATAGCTCT 360
AAAAATAGGA TCCACCCACC ACTGCTCAGA AGGCTGCTCT GCTAGTCATT TCTAGAACAT 420
TCTGTGCCAC TGTCCATCTT AAGGTGGGTG GGGGCCCAGG TGTTGAGACT CTATCATATC 480
CTCTCCTGGT GCTTATGTTT GAGAGAACAT TCGAAAGATT CTCAAGTTCG GGAATTTGGG 540
CCTCCAGGGA CCTCTGTGTA AAAATTGTAA CTATGATGGG TATTTTCCTG GGGCCATCCA 600
TTCCTGCAAA GTGACATGGA TGTGCTGTCC TCTGTGGGCT GTGTCTGGAA ATAGGTAGCG 660
TCGGACTGTT GAGGCAGCAA CCCCAGGACA TAATCCCCAT ATAACGTGGC TCTCTGGAGC 720
AGGCCCAGAC CCTCCCGCAG GGCACGCACA GCCCCAGCCA CACCCCTGGG CGGGAGCCAC 780
AGAATTAGCA CAGTCATCTC GGACTGGGAG GGCCAGAGAC TCATTGCTGG TAATGTGAGA 840
GAGGCCTGGC AGCGCCTGAG GGGCACAGCT CAGAGTCGAC GAAGAAAGGG CCTTTGTCTG 900
AGTTCATGTC CTCCTCGGGC GCAGTGGCGC CCCTGCCGTG GACGGCTGGT CGGCCTCGGA 960
GTGGACAACA CTTCCACAGG GAGCACTATG TGGACAGGAC AGCTGGCCTT CTGGCCACCC 1020
AGTCCCCTCA GATCGCCAGC AAGGGAAGGA CAGAGACCCT GGCCTGGGTC TGTTTCAAGC 1080
CCTCTTCTGT ATGAAGGATG CTGCCCAGGC CAGCAGCGCC GCCCACCTCT GGTGCCCACC 1140
TTTTCCACCC TTTGCTTTCT GGTCCTTCCT GCTAAGGGTT CTCTTGGCTG CAAGCTCAAG 1200
CCTCAGTGCC ATGGCCTTTT TAGACAGTGT GGGAGACAGT TCAGAGCTCT GAGCTCTGTT 1260
GAGAAAAGAA AACTGTTTCT GCGTTTGGCA AAGGTGTGGG TTGTCAGCAG AGATCAAAGT 1320
TCTGTTCCTG GCAGGGTGAG CACCTGTGAC ACACCTTGCC CCTCCCCCTG CGCCAATCCC 1380
AGAGAGGCGG TGGCATTTCT GACCCTTCCC TTCCACGGCA 1420
|
