Tag | Content |
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EnhancerAtlas ID | HS133-00498 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:17880500-17881380 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:17881051-17881069 | CCCTCCCTCCCTCCTTTC | - | 6.17 | EWSR1-FLI1 | MA0149.1 | chr1:17881056-17881074 | CCTCCCTCCTTTCCTTCC | - | 6.72 | EWSR1-FLI1 | MA0149.1 | chr1:17881064-17881082 | CTTTCCTTCCTTCCTTTT | - | 7.36 | EWSR1-FLI1 | MA0149.1 | chr1:17881060-17881078 | CCTCCTTTCCTTCCTTCC | - | 7.79 | ZNF263 | MA0528.1 | chr1:17881052-17881073 | CCTCCCTCCCTCCTTTCCTTC | - | 6.31 | ZNF263 | MA0528.1 | chr1:17881047-17881068 | GCCTCCCTCCCTCCCTCCTTT | - | 6.76 | ZNF263 | MA0528.1 | chr1:17881056-17881077 | CCTCCCTCCTTTCCTTCCTTC | - | 7.18 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_01537 | chr1:17876984-17882768 | Aorta | SE_03096 | chr1:17880648-17881152 | Bladder | SE_26573 | chr1:17877125-17882739 | Esophagus | SE_34117 | chr1:17880087-17881321 | HCC1954 | SE_65277 | chr1:17880439-17881339 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I017553 | chr1 | 17879916 | 17881108 |
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Enhancer Sequence | ATGAAAGCTG GACTTCAAAG ACCAGAGGAA GTGCAGAGGA TACGTTTGCT AGGTGCTTCC 60 TTGTGGGGGT GGGTACGGCC TCTCTACCTC ACGTCCCATC ACTTGGAGCT CTCTGCAAAA 120 CCCGTTCTCC CGGGCCCTAG ATGCAAAAAT CCACCCAGTT CATCCGCCCT TGAGAAATGA 180 TGTTGAGTCA GATCTGGAAA CACTAAATGG GTGAGTCACA GTGAGGATGG TGAGGGGCTG 240 GGCAGGGAGG AACAGTGCTT AGCCCACCAT TGGCCAGAGC TCAGCCTTGC CAAGGAGCCC 300 AGCCCAGGGG GCAGGCCTCA GCTATTTACA GAGAAGGGGA CTTGGGAGCA GAGAGAGGAT 360 GCGGCTGGCA GGGAGGGAGA CAGAGGAGCT GAGGGTCAGA CAGCAGAGCT AGAAGAGTTT 420 TCAGGGATCA TCTAGTCCAC ACATAGGACA TCTCAGTCCC AGAGAGGGGC TGGGACTTAC 480 CCTAGGTCAC ACAGCCCATG ATGCCAGACC CAGCAATAGA AGGGGATTTT GGGAGGCTGA 540 ATCCTCAGCC TCCCTCCCTC CCTCCTTTCC TTCCTTCCTT TTTTTTTTTT TTTTTTTTTT 600 GACAGGGTCT TGCTCTGTCG CCCAGGCTGG AACACAGTGG CATGATTACA GCTCACTGCA 660 GCCTTGATTT CCTGGGCTCA GGTGATCCTT CAACCCACCT CAGCGTACCG AGTAACTGGA 720 GCTACAGGCA CATGCCAACA TGCTAAGCTA GTTTTTGCAT TTTTTTGTAG AGATGGGGTT 780 TTGCCACGTT GCCCAGGCTG GTCTCAAACT CCTGCGTTCA AGCGGTCTTT CTGCCTTGGC 840 CTCCCAAAGT GCCTGGATTA GAGGCATGAG CCACTGTGCC 880
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