Tag | Content |
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EnhancerAtlas ID | HS133-19191 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:44844300-44845460 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:44844316-44844334 | GAAAGGAAGGAGGAAAGG | + | 6.63 | EWSR1-FLI1 | MA0149.1 | chr20:44844320-44844338 | GGAAGGAGGAAAGGAATG | + | 7.33 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33635 | chr20:44842417-44845470 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I046215 | chr20 | 44844329 | 44845395 |
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Enhancer Sequence | AAGACGGAAA GAAAAAGAAA GGAAGGAGGA AAGGAATGAC GAGCAGGAAA GCAAACCTTC 60 TGGGGGCCCT GGCCTCCTCT CTGCTCTGCC CCACCCCTTC CAGTTCAGAG CTCATTCAGA 120 GCCTGGCACA AGTGGGCAGA AGACTGGGTG GGGGTGCGTC CCACCCATGC CACCCGTCTG 180 CATGGGGCTG CCTTCAGGGG CTGGGGCTGG GCTGGGAGAT TGGGCAGTGG GATGGCTTCT 240 GTGCCAGGCT CCCTGGCACC GGGAAGCCGG TTGGTGAGCT CAGCTCACTC CGCTCTGTGT 300 CTGAGCTGAG GCTGTAGGCC ACAATGATGC TGCGCTCTCA GCTAAGGGAT TGGATTCCCT 360 TATCTCTCGG GGGTCAGTCC CCTGTGGCGG GGCCTAATGT GAGAGCAGCA GACCTCAAGT 420 AATGACTCAC CCGATAGGAA TCAGCCCAGC TCCTGCGGCA TTTAGTCCCT GCCAGCTTTG 480 GTGGCTTCCC TGTAGTGGCT CTCGGCCTGA GCCTGGGACA GAGGGGTTGG CTGGGCTGAT 540 AGGGAGCTGG GAGGCTGGGC CGGAGACATC CCCCAACCCC CGCTGTGCCA GCAGAGGCAG 600 AGGGTGGAAA GGCCTCCTAA TTCAGAAGCA CAGAGTCGCG CTACCCAGGC TCAGAGGAGG 660 AGGGAAATGC CTGTCACTCA GACTTAGTTT TTCTCTGCAC AACCTCTATC TGTCTGGGGG 720 CTGAGCTGCC TCTGCCTAGA TCCCTGGGTG CCCCCTTTCT CCCCAGTACC TTCCCTCTGC 780 AAGCCTAGGT CAGCGGCATG GGATGGCCCA ACAAGTGGCT AGGGGAGTGG GCAGGGGCCA 840 GTGAGGGGTT GGAGGATGGA CGGAAGGGTG GATGGGTGGG GCTCCCCCTC TGCCGGAAGC 900 AAGAGGAGGT CTGGGAAGGT GATGGTGTGT TACTTGGCTC TGTGGAGCAT CGGACAGCCC 960 TGGGGTCTTC CTTGGTAGGA AGCATGGTTG GAGGGGGGCT GGGGGATAGC TGGTGGCTTG 1020 GGAGGACAGA CAGACAGACA GAAAGAGAGG GGGAAGCCCT TCTTTTGGTG GGAAGTCTAA 1080 AGGGAAGCTG GGGTCAGCAG GTGGCTTGGA TGGGGTAACA GACAGACACA CAGACGCGCC 1140 TTCCTCTGGG AAGGCCTCAC 1160
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