| Tag | Content |
|---|
EnhancerAtlas ID | HS129-23561 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr21:38090640-38092120 |
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 | GGCTGGGTTG TCCTGTTGCG TGAGGTGGCA CCGTCAGGAT GGCCACTTTG CAGATAATCA 60
TGTTGTCTCT CCTCTGATGG AGAGCCACAG GCTCCCAGCG ACACCTGCAG CAAGACACAC 120
CTAAAAATAA CAAGGGGGTG GCTCGGGACA AGACACACCA TGAGCCTCCT TTTGTTATCT 180
TGAGTTACCC TCTCTCCTTC CGGCAGGGTC AAGAAGGAAT TCTCCAGACC TACCCAAGAT 240
CCTTCGCCAC CCAAGGACGG TTTCCCACAT GCTTTGAGTT TCTTCTCAGG CTGGGCACTG 300
GGACTCCCCT TGGTGGTGGA GGAAGTCCTA CCACTGCCCC TGGGCCTCCC CTGAACAATG 360
CTGGGGTTCA CCGACTCACT GTCCTTGTCT GCCACCCTCA GCACTATTGA TTATAGCTCT 420
AAAAATAGGA TCCACCCACC ACTGCTCAGA AGGCTGCTCT GCTAGTCATT TCTAGAACAT 480
TCTGTGCCAC TGTCCATCTT AAGGTGGGTG GGGGCCCAGG TGTTGAGACT CTATCATATC 540
CTCTCCTGGT GCTTATGTTT GAGAGAACAT TCGAAAGATT CTCAAGTTCG GGAATTTGGG 600
CCTCCAGGGA CCTCTGTGTA AAAATTGTAA CTATGATGGG TATTTTCCTG GGGCCATCCA 660
TTCCTGCAAA GTGACATGGA TGTGCTGTCC TCTGTGGGCT GTGTCTGGAA ATAGGTAGCG 720
TCGGACTGTT GAGGCAGCAA CCCCAGGACA TAATCCCCAT ATAACGTGGC TCTCTGGAGC 780
AGGCCCAGAC CCTCCCGCAG GGCACGCACA GCCCCAGCCA CACCCCTGGG CGGGAGCCAC 840
AGAATTAGCA CAGTCATCTC GGACTGGGAG GGCCAGAGAC TCATTGCTGG TAATGTGAGA 900
GAGGCCTGGC AGCGCCTGAG GGGCACAGCT CAGAGTCGAC GAAGAAAGGG CCTTTGTCTG 960
AGTTCATGTC CTCCTCGGGC GCAGTGGCGC CCCTGCCGTG GACGGCTGGT CGGCCTCGGA 1020
GTGGACAACA CTTCCACAGG GAGCACTATG TGGACAGGAC AGCTGGCCTT CTGGCCACCC 1080
AGTCCCCTCA GATCGCCAGC AAGGGAAGGA CAGAGACCCT GGCCTGGGTC TGTTTCAAGC 1140
CCTCTTCTGT ATGAAGGATG CTGCCCAGGC CAGCAGCGCC GCCCACCTCT GGTGCCCACC 1200
TTTTCCACCC TTTGCTTTCT GGTCCTTCCT GCTAAGGGTT CTCTTGGCTG CAAGCTCAAG 1260
CCTCAGTGCC ATGGCCTTTT TAGACAGTGT GGGAGACAGT TCAGAGCTCT GAGCTCTGTT 1320
GAGAAAAGAA AACTGTTTCT GCGTTTGGCA AAGGTGTGGG TTGTCAGCAG AGATCAAAGT 1380
TCTGTTCCTG GCAGGGTGAG CACCTGTGAC ACACCTTGCC CCTCCCCCTG CGCCAATCCC 1440
AGAGAGGCGG TGGCATTTCT GACCCTTCCC TTCCACGGCA 1480
|
