Tag | Content |
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EnhancerAtlas ID | HS062-03582 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:13068850-13069980 |
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) |
CTCF | MA0139.1 | chr12:13069331-13069350 | TTTCCACTAGATGGCGCTG | + | 7.32 | EWSR1-FLI1 | MA0149.1 | chr12:13069501-13069519 | CTTTGCTTCCTCCCTCCC | - | 6.42 | EWSR1-FLI1 | MA0149.1 | chr12:13069794-13069812 | GCTTCCTTCCTTCATTTC | - | 7.16 | TEAD1 | MA0090.2 | chr12:13069117-13069127 | ATGGAATGTG | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38847 | chr12:13067670-13071234 | HUVEC |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I012915 | chr12 | 13067982 | 13070805 |
|
Enhancer Sequence | GCTCATTTGA GCAGTACCTG TCACCCCTCC TCCCACTGCT GCGGCTGTTA ACTCATCTTC 60 AGGTCTCACA CCTTCTGCAC ATAAATAAGC TATTTTTAAA AGTTATTATT TTTTTACTCT 120 TTCTTTTCTT TGGAGAGGGT ACCAAAGGAT AGCTGTTCTG TTTAAGTAGG GACCTCTCAT 180 GGCCTACAGG CTTTGACATC TGAGAATCAA ACTGGAGAAC ATTCCGAAGC CGTTCTTATA 240 AGTGTCTCCA TCTCTACCTG GGCTGAAATG GAATGTGCAA ATGTAGCCCA GCCTGGTCCT 300 TGGGTGTTGC CAGTTGATTG ATGACTGGGA GCCAAAGTGG CATCTCCTTT GACCTAAACG 360 GGCGATGATG AAATAAAACT CAACAGCCTT TCTCTCATCT TGCATTGTGA GATGCGAAAT 420 AGAGCGTGTC TCTCTGCCTC TCATTTTAGG CTGAGGCCGT CCAAAGCGGC CATGCCCCAT 480 GTTTCCACTA GATGGCGCTG ACACTTCAGG CATCAACCCT CATGGCCTCT CAGCCTTGCA 540 AAGGCAGCCA CTTAAAGTCG GTGTCCTGTG TGGGGCACCA AGCTGAGCTG CAGACACCCA 600 GTAGGCGCGA GGCAAATGCG TCCCATTTTA AGAGGCTTGT ATTTATGAGC TCTTTGCTTC 660 CTCCCTCCCA CTAACTTTAA AGAATTGCTC TCCATCTCCT TTGGCAAAGT TCCTTTGCCC 720 TTTGTCTTAT TTTTGTGAAA CCCTCCAAGG TATTTCCAGT CCATTTGCAT CCAATCTGGC 780 ATCTTTACGG AGAGCGGTCT CATATGCTAT TGTTGTTAAC GTGGACTAGT ATTTATGTGT 840 TGAGAACACT GGCTGTTTGT CAGGAAAAGT GTGCCAAAAC AAAGAGTACG GCCGGCCCTG 900 GAAATGCATC AGCAAAACCC ATTTCCCCCG TGCACTCATT CTGAGCTTCC TTCCTTCATT 960 TCTGTCATTA CTGCTGAGAA CTGGACTGTG CCCAGCTGAC CTTTCCCTTC CTTGCCCTCA 1020 TCTTGCTGCC AGGGTCTGCA GGTTTGCCAC CGTCCCGGCC CCAGTCTGAA ACATGGGATT 1080 ATTTCAGAAT TGGAGGTGGC AGCTTCAGAA AAAAATCCTT CTCGTGTGTT 1130
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