Tag | Content |
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EnhancerAtlas ID | HS080-02640 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:183163730-183164750 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I183194 | chr1 | 183163373 | 183169370 |
|
Enhancer Sequence | TTTTAGTACA AATTAGAATC TCCTTTTTAA CTTCTCTTTA TTCAGACACA TCATAGAAGG 60 TTTCTTTCCT TTTGGTCCTC TTTGCTTCAG GTATTTACCT CTGGCATCCC TGGAATCTCT 120 GATTCCCTTT ATTTCAACTG CTTCTTAGAG GGGCATAGGA TACCTTTTTC TAGGCCATGC 180 AAGAAATGTC CAGAGAACAC TATGCTCTTT GAATAACAGT TAAATGTCCT TTCTATGCTG 240 GAATGCTTTT CTTTGTAGGT AACTTCACAG AAATGTATAA CCCTTTATTT CTGTGGTCAG 300 AAGAGTGTGG AGTTCCATGG AGGTGGTTGC TGTCATATAG AATCTTACCA CAATCACTTC 360 CTGAGTCTAT GCTGCAGCTG ACAGCAGCTG TCTTGCGGTA GAGCCTTTGA CAGTGCCAGC 420 TATAACTCTA ATGTCCTCAG TTTGCCTTCC CTTTCACCTG TGAGCTTACT CAGACTGAAC 480 CCTCAGTTTT ACCTTTACCC TCCACTCCTT TGCTAGTCAG ACAAAACTTG GTGTCCCCAG 540 TTTCCCTGTT CACTGGGACT TTCTTCCCCC TCCTCATTGT CTGCCTGGGC ACTGGTGTCC 600 CAGTGGAGTG TCAGGGGAAG ACATCTCCAG GTGTGAACTC CTGATGGAGT CCTCACCAGG 660 CTGAGTCATC TACAGTTCAC ACGGGTACAT TCCCAAGTCT AGGCTGTGAT ATAATGTACT 720 ATGAACTCTC GGTGAAACAG GTGTCTCCTC TGAAGCCATA ATCATTCAAA AGGAAATGGC 780 AGTGATCTGA GTTTCACTGA CTCTTGATGA CTTTGGAGTA TTCAGAGTTG AAAAAACTGA 840 CCCATACTTT ATGATTCAAA ATTGCCTGTG AGATTAGAGA ACTGAGCTCT GTCATTCCTC 900 TCATCCTAGC ACTTCCTGCC TCAGCCTTAC TCACATTGCT TGGACATTTA AATGTCAACT 960 GGTGCCGTGC CCTTTATTTA AATGAAACAA ATGGATCAGG CAGGATATGG TATCAGTTTT 1020
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