Tag | Content |
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EnhancerAtlas ID | HS062-16118 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr8:130693640-130694780 |
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 | chr8:130694326-130694337 | CAGCAGCTGTC | - | 6.14 | Tcf12 | MA0521.1 | chr8:130694326-130694337 | CAGCAGCTGTC | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40042 | chr8:130694212-130695113 | K562 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I129681 | chr8 | 130693842 | 130696246 |
|
Enhancer Sequence | ATAGTAAAAC TCCGTCTCTA CTAAAAATAC AGAAATTAGC CAGGCATGGT GCCTGTAATC 60 CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TTACTTGAAC CCGGGAGACG GAGGTTACAA 120 GATCATACCA CTGCACTCCA ACCTGGGTGG CAGAGCAAGG CTCCATCAAT ACATACATAC 180 ATACATACAT ACATACATAC ATGACTTGGG TTTGAGTTCT GATCACCACA TTAGAGCAGG 240 CTGACTTGAA AAAACCACTT TCCCATTTAC CCTGAGACTC TGCATCCTCA TCTGCCGAAA 300 CTGACAATTT TGCTTCTACC GAACTGAAAG GGTAGTTTCA AAGATGAAAT GAATCAATGT 360 GTATGAAAGC TCTTTTAAAA CCATCATGTG CAAATATAAA TTCCTCCGAG AAATTGGTCT 420 TGTCCTAAAG ATGGCCCGGG TTGCCCTCTT ACCCTAAAAG TCTCCTTATT CACTCCCAGC 480 CCGCCTCACT CGTTCATCAT TGCAGGAAAA TGTGCCAAAG ATCAAAAACA GGTGAGATCC 540 GACCCCAGGG ACAGAGCAAA GAAGTAACTG GACTGTAGGC ACCAGCTGGT CCTGTTCTGC 600 CCTGCCCTCG TAGAACTGTG AACAGCTAAG AAGTGCTGTT CCTTTAAACT TTGCCCCTTT 660 GTGGCTCACA GATGAGTAGA TTCAGGCAGC AGCTGTCAGC TCTGCAGGCA GCAGAGAATC 720 TTTCCAGAGC AGCATTCCCA GCAGTGTCAG GATGGGAGGA TGAAATTAGG TGAGCCAAGC 780 AACCTGAAAG TCCTCATTCA AAAGCCTCTA CTGCCATCTA CTGCCTCTCT GAAGAACTCA 840 TTGGCAAAAA GCCAAGAAAA GACTGCAATG GAGGTGGGGT AGAGAGAAGC CTTAGCAATA 900 GACTGAATTG TCTGGATCAA TTAGTCCACC CTTCATTCTC CAGCTGGGGA AAATGAGACC 960 CAAAGAGGTA AAGAGGCTTG TCTGAAGTCA CTCTGCTAGC CCACGGCAGC CCATCATCTC 1020 TTGGATACAC ATATTAGCTC TGCCCCACAA CACACTGTTT CTGTCTGAAT ATATAAACTA 1080 TCAATAAAGC TGGCTTAGAG CAAAGAGGTT TGTGTGGTTG TTATTATTGA GACAGGGTCT 1140
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