| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40822 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:170733750-170734720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:170734007-170734022 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27743 | chr3:170731261-170747526 | Fetal_Intestine | | SE_28704 | chr3:170726524-170747601 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I171013 | chr3 | 170731221 | 170738602 |
|
Enhancer Sequence | CATTCCTCTC AATGATGATT TGGTCACTAT TTAGCATCAG TGAGCTGGGA GGGTACTCTC 60
TGAAAAGGAC CTGGAATGCA GCTGCTCTGG GTTACTAGTT ATGGGCAAAG GCCTGTTTGG 120
TAATGCCAGC TGAGGGAGGG GAAGAATTGA GCATCCTCTT ATAAAAGAAG TCTGATCAAG 180
ACATTTGTCT CAGACTGGGT GCCGTAGCTC ATGCCTGTAA TCTAGCACTT TGGGAGGCCA 240
AGGTGGGCAG ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGGCCAACG TGGCAAAACC 300
CTGTCTCTAC TAAAGATACA ATAAATTAGC CAGGCATTGT GGCTGGAGCC TGTAATCTCA 360
GCTACTTGGG AGGCTGAGGC AAGAGAATTG CTTGAACTCA GGAGGCAGAG GTTGAAGTGA 420
AAATCTCCAG CCTGGATGAC AGAGTGAGAC TTTGTCTCAA AAAACTAAAA CAAAAACATT 480
TGCCTCACTA GAAGGCTGCC TTATATGAAT AATATGCATA GAAAAAAAAG CTGAAGGAAA 540
TATCCAAAAT GTTCTCAGCA AATAATTATG GGTATTTTTT TTTCTAATAC TGTCTTCAGT 600
AGGCATGTGT AATTTTCATA ACCATATGAA AGTGTGATTT TAAAATCCTT CCAAATAATC 660
CCAAATGTCA TTCAGCTGAT TAAAAAAAGG CTTAAAAAAT CATTCTTATG TAATGGTGTT 720
TCAGCAGCTC TTTAAATACA AAAGGAAGGG CCTATATAGA GAGAGAGCAC TAACCTGGAC 780
GCCAGTATGG GGATCGCTGT TTTCAGCTCT GGCTCTGGGA CTTGGATTGA AGGAGGTGAA 840
ACCTTAGCCT AAGCTTCCGT CTAAGACTGG AGGGGATGGT TTAATTTTTT CTTTTTTTTT 900
TTTTTTTTTG AGATGGAGTT TTGCTCTTGT TGCCCAGGCT GAAGTGCAAT GTGCGATTGC 960
AGCTCATCGC 970
|
