Tag | Content |
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EnhancerAtlas ID | HS147-04237 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:201998240-201999260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr1:201998401-201998415 | ATGACTCATCTATT | - | 6.04 | JUN(var.2) | MA0489.1 | chr1:201998396-201998410 | AAAGTATGACTCAT | + | 6.14 | RUNX1 | MA0002.2 | chr1:201998600-201998611 | AAACCACAGAG | - | 6.14 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_24689 | chr1:201998537-201999104 | Colon_Crypt_3 | SE_26730 | chr1:201998431-201999363 | Esophagus | SE_27624 | chr1:201998627-201999568 | Fetal_Intestine | SE_28545 | chr1:201998471-201999537 | Fetal_Intestine_Large | SE_33417 | chr1:201998080-201999564 | H2171 | SE_33792 | chr1:201997988-201999604 | HCC1954 | SE_34304 | chr1:201998273-201999620 | HCT-116 | SE_34741 | chr1:201997167-201999725 | HeLa | SE_52354 | chr1:201998461-201999352 | Small_Intestine | SE_56834 | chr1:201998555-201999441 | VACO_400 | SE_57376 | chr1:201998654-201999322 | VACO_503 | SE_65333 | chr1:201998512-201999617 | Pancreatic_islets | SE_67013 | chr1:201998080-201999564 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I202028 | chr1 | 201997608 | 201999492 |
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Enhancer Sequence | CAGATATTTT TCTGATTTTT TTTTCTTTAA ATTAAAATTG GTGTTTCCTC GGGGGAAAAA 60 AAAAGAAGAA AATTCTTCCT TCGTTTTGAA AAATAAACAT TAGTAATTCA AAAAAAGTAA 120 AATAAACAAC ATGTCTATAT TTGGAATGAG TTAACCAAAG TATGACTCAT CTATTTCTAC 180 TATGGAATAC TATGCCTTCA TTAAAAATGA TGATTCATTG AAGAATCTGC TTTGTGCCAG 240 GCATTGATGA TATAAAAGAA ACCAAGATGA GGACTCTCCC CTCTTGAGGT TATATGAGTA 300 AACAGATGCT TAACACATAA TGGGAATAAT TGTATGACAA AAGTATCTAT AGTGACACTG 360 AAACCACAGA GAAGAACACA GACTCTGGAA CCAGGTGCGC GGGGGTTCTG GGAAGATAAG 420 TAGGAACTCA CCAGGGCACA GAGATGGGGG TCACCTAGGC AGAAAGAACA TCACGTGCAA 480 AGGTCAAGAT GCATGAAATG GTACGATTTA AACAGAGGAC AGGAAGAAAT TGAATAGGAT 540 AGGAGCCTAG CATTTCAGGC AGGAGTGGCC AAAAATGAGG CTGAGAGATT TGTAGATCAT 600 GAAATGTAAG GTAACAGAGT CAAAATAGCT TTTTGGTAAT GTCTCACTGA TGGCAATGTG 660 GAGGGTAGCA TGATGGGATA GTATTAAAGA AAGGACACCA CCCAGAAAGC TGTTACAGTT 720 CCCAAGAAAA GGGGATGAGG GCCTGAGTGG CAGCAATGAC AGTGGAGATG AGGACTGGAG 780 TGGAGCAAAG GGTCAGGAGA CATCACAGAG GTCTAAAGGG CAGGACTTGG TGAGAGGTTA 840 AGGGGAGGGC AGAGTCAAGA TAACACAGAG AGTCTGACAT GTGGCTGGGT AGGCCAGGCT 900 CCGGTCCTTA GGAGGAAGAA CAGATTGGGG GCTGGATCTG ATTACTGCGC TTTGAGGGGC 960 CTGAGATATT CTGTAGGCAG ATATGTTCAG AGGGAGGCTT GGGTCAAAAA GTAGCTTTTA 1020
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