| Tag | Content |
|---|
EnhancerAtlas ID | HS187-01966 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:183163740-183164790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35834 | chr1:183163338-183165417 | HMEC | | SE_64350 | chr1:183163237-183165340 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I183194 | chr1 | 183163373 | 183169370 |
|
Enhancer Sequence | AATTAGAATC TCCTTTTTAA CTTCTCTTTA TTCAGACACA TCATAGAAGG TTTCTTTCCT 60
TTTGGTCCTC TTTGCTTCAG GTATTTACCT CTGGCATCCC TGGAATCTCT GATTCCCTTT 120
ATTTCAACTG CTTCTTAGAG GGGCATAGGA TACCTTTTTC TAGGCCATGC AAGAAATGTC 180
CAGAGAACAC TATGCTCTTT GAATAACAGT TAAATGTCCT TTCTATGCTG GAATGCTTTT 240
CTTTGTAGGT AACTTCACAG AAATGTATAA CCCTTTATTT CTGTGGTCAG AAGAGTGTGG 300
AGTTCCATGG AGGTGGTTGC TGTCATATAG AATCTTACCA CAATCACTTC CTGAGTCTAT 360
GCTGCAGCTG ACAGCAGCTG TCTTGCGGTA GAGCCTTTGA CAGTGCCAGC TATAACTCTA 420
ATGTCCTCAG TTTGCCTTCC CTTTCACCTG TGAGCTTACT CAGACTGAAC CCTCAGTTTT 480
ACCTTTACCC TCCACTCCTT TGCTAGTCAG ACAAAACTTG GTGTCCCCAG TTTCCCTGTT 540
CACTGGGACT TTCTTCCCCC TCCTCATTGT CTGCCTGGGC ACTGGTGTCC CAGTGGAGTG 600
TCAGGGGAAG ACATCTCCAG GTGTGAACTC CTGATGGAGT CCTCACCAGG CTGAGTCATC 660
TACAGTTCAC ACGGGTACAT TCCCAAGTCT AGGCTGTGAT ATAATGTACT ATGAACTCTC 720
GGTGAAACAG GTGTCTCCTC TGAAGCCATA ATCATTCAAA AGGAAATGGC AGTGATCTGA 780
GTTTCACTGA CTCTTGATGA CTTTGGAGTA TTCAGAGTTG AAAAAACTGA CCCATACTTT 840
ATGATTCAAA ATTGCCTGTG AGATTAGAGA ACTGAGCTCT GTCATTCCTC TCATCCTAGC 900
ACTTCCTGCC TCAGCCTTAC TCACATTGCT TGGACATTTA AATGTCAACT GGTGCCGTGC 960
CCTTTATTTA AATGAAACAA ATGGATCAGG CAGGATATGG TATCAGTTTT CTGGCTGTGG 1020
TGGCTTAAAA TGTGGCTATG AAAAATTTGC 1050
|
