Tag | Content |
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EnhancerAtlas ID | HS133-19501 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:52768280-52769680 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:52769407-52769425 | GGAAGGAAGCAAGAGAGG | + | 6.69 | ZNF263 | MA0528.1 | chr20:52768938-52768959 | GCTTCTTTCCCTTCCTCATCC | - | 6.34 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_34280 | chr20:52768097-52769961 | HCT-116 | SE_36154 | chr20:52768655-52769915 | HMEC | SE_64506 | chr20:52768648-52769956 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I054148 | chr20 | 52764817 | 52769776 |
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Enhancer Sequence | TTAGTAGAGA TGAGCAGTAC ATGACGTGCA TCCCACAGGT CCGGGAACCA ATCTATCTTT 60 GTTGGAATCC TGGCTTCCCT ACATACTAAC TGTGATTCTA AGGAGATTAC TGAGCACCTC 120 TGTGCCTCAG TTTCCCCAGG TGTGAAATGG GAAGAATGAT CACATCTACT TACAGGGCAG 180 TGACAAGGAT TTGTGAATTC ATATGTAGCA AGTGCACAGA GGAGAGACTG GGGCAGCAAG 240 ATCAGTCAAT AAATATTATT ATCATCATGA CCACATTGGC CATGTCAGTG TCGGCTCCAG 300 GCAACCTGCT CAGGGAGGTG AGGGGCAGCA GACGTGGCCC TTGCTCCACC CTGTGCTCCT 360 CACACCCATT TGCCGGTCTT TGTGCCCTTC GCCCAGGTTT TTCATGCTTT GCTCCTCATG 420 GCTGGCACCT GCAGCCTTCT TCAAAGACTA CCTTCTGGCT ACTATAGCCA TTTTGCCTGG 480 ACATGTAAAG TCTAGAAGTA TCTTAGAGTT TATACCCCAA GGTGCAGCCT GAACTGAAGG 540 AGTGTGGAAG CCCTGCTCCC TGGGCACAAG GAGAACAAAC TGAGCTGCAA TGTACACTCC 600 AGAGCTCCCA GAGATCAGGC TGAGGCTGGA ACTTCACTCA AAACCACACG CTTGTTTGGC 660 TTCTTTCCCT TCCTCATCCT GCTGTCCCCA CAGTCGCACA GGTCTCCTTG GGAATCACAA 720 CCCTAATGAA TCCCGGTGCT GGGGACAGCC CCTGTGGGAT CTAAGTCATC AAGGAAGATT 780 TCCTTCAGGA AATGAAAGCT GGGTGGACGT AGATGGTGCG TAGGAGAAGA ACAGGCAGAG 840 AAAGAGCATG CCGGGAGGGA GACGGTGGGA AGAACCCTCT TGCTAGCATT TAAGGAACAG 900 CAGAAACTGG CAGAAGCCAC TGTGGCCTGG TTCCAGAGGC CTCTGGGGGT GGATGATGTG 960 GGCTGAGGCC TGGGGGATCA GTGGGACCTC AGTTGATAGG GCCTGGAAGT GTGGATTGCA 1020 GAATCGGATC TTTACGTAAG AGCAATGGGA AGCCCCAGAG GCAGGATGAG GCATGATCAG 1080 GTTTGGGTTT GAAAAGACCA GTAAGGCAAG TGTGCAAAGA ACAGAGGGGA AGGAAGCAAG 1140 AGAGGACTGA GATCAGCTGG GAGCTCCTGC AGAGACTAGA GATATTAGTG GTCCAGGCAA 1200 GAGATTGTCA GTATTGCTCC CAGCCACGGA AAATTTGGCT GTTGTAGGTC TTTCATTGTG 1260 AAATGTAAAC TTATTCTTGG GAATTAAGTA TTCAAACAGT GAATGTGGTA GGCAGGGGCT 1320 GAAATGGTTC GTAACCTCTA CCTGACTGCC AAGTGCCAGC CTCCCTTTCA TGTCATGAAA 1380 GATACAAGAG AGAACAGGCT 1400
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