| Tag | Content |
|---|
EnhancerAtlas ID | HS133-20556 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:38091080-38092120 |
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 | ACTGCTCAGA AGGCTGCTCT GCTAGTCATT TCTAGAACAT TCTGTGCCAC TGTCCATCTT 60
AAGGTGGGTG GGGGCCCAGG TGTTGAGACT CTATCATATC CTCTCCTGGT GCTTATGTTT 120
GAGAGAACAT TCGAAAGATT CTCAAGTTCG GGAATTTGGG CCTCCAGGGA CCTCTGTGTA 180
AAAATTGTAA CTATGATGGG TATTTTCCTG GGGCCATCCA TTCCTGCAAA GTGACATGGA 240
TGTGCTGTCC TCTGTGGGCT GTGTCTGGAA ATAGGTAGCG TCGGACTGTT GAGGCAGCAA 300
CCCCAGGACA TAATCCCCAT ATAACGTGGC TCTCTGGAGC AGGCCCAGAC CCTCCCGCAG 360
GGCACGCACA GCCCCAGCCA CACCCCTGGG CGGGAGCCAC AGAATTAGCA CAGTCATCTC 420
GGACTGGGAG GGCCAGAGAC TCATTGCTGG TAATGTGAGA GAGGCCTGGC AGCGCCTGAG 480
GGGCACAGCT CAGAGTCGAC GAAGAAAGGG CCTTTGTCTG AGTTCATGTC CTCCTCGGGC 540
GCAGTGGCGC CCCTGCCGTG GACGGCTGGT CGGCCTCGGA GTGGACAACA CTTCCACAGG 600
GAGCACTATG TGGACAGGAC AGCTGGCCTT CTGGCCACCC AGTCCCCTCA GATCGCCAGC 660
AAGGGAAGGA CAGAGACCCT GGCCTGGGTC TGTTTCAAGC CCTCTTCTGT ATGAAGGATG 720
CTGCCCAGGC CAGCAGCGCC GCCCACCTCT GGTGCCCACC TTTTCCACCC TTTGCTTTCT 780
GGTCCTTCCT GCTAAGGGTT CTCTTGGCTG CAAGCTCAAG CCTCAGTGCC ATGGCCTTTT 840
TAGACAGTGT GGGAGACAGT TCAGAGCTCT GAGCTCTGTT GAGAAAAGAA AACTGTTTCT 900
GCGTTTGGCA AAGGTGTGGG TTGTCAGCAG AGATCAAAGT TCTGTTCCTG GCAGGGTGAG 960
CACCTGTGAC ACACCTTGCC CCTCCCCCTG CGCCAATCCC AGAGAGGCGG TGGCATTTCT 1020
GACCCTTCCC TTCCACGGCA 1040
|
