Tag | Content |
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EnhancerAtlas ID | HS133-23538 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:194800280-194801920 |
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) |
RUNX1 | MA0002.2 | chr3:194801156-194801167 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr3:194801313-194801324 | AAACCACAGAG | - | 6.14 | ZNF263 | MA0528.1 | chr3:194801271-194801292 | GGGGGTGGGGGGGATGGGGGA | + | 6.26 | Zfx | MA0146.2 | chr3:194801793-194801807 | CAGGCCCAGGCCCC | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_49978 | chr3:194799439-194803358 | RPMI-8402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I195079 | chr3 | 194800281 | 194803228 |
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Enhancer Sequence | AAACAAGGTA GGTACTATGA TTTCCATGTT CTAGATGAGG AAGCTGAGGC AGAGAGCTCT 60 AAAACGCTTG CCCGAGGTCA GCAAGGGGAG AATTGCCAGG CAGAAGAGCT GTCCGGGAAG 120 AGGGAACCCT GGGATGTGGC TGGGAGCAGA GAGGGACAGA AGCGAGGACA GCAGCAGTTC 180 TGAGAGGTCA GGAAAGGAAG ACATGAAGTC ATCTAAGGAG GAGGAGGGGC TGGGTGTGAG 240 AAGGGTTTGA GAAAGAGAGA ATCTGTTTAC AAGGGGCTCT GTGTAATACA ATCGGGAATG 300 AATAACAGGC AAATAAAGGG TGAGGGTGTG GGCAGAGTCA GGTGACTCTG GGACTGATAA 360 GGGGAAGTGT CCCGCTCATC TTCATGTCTG GAGGGCCTGG CGTGGGCATC TGATTCACAG 420 AAGGGCCCCC AGAACTGTTA GTTTCAAATG GATGGATTAA TGAAGGAAGG CATAAGAGAT 480 TCTAAAGCTA GATGGCAGGA ATTTAGGAGA ATGTTGGATG AAGGCAGTGG CACAACCGTT 540 CAGAAAGGCA GGGGCGGGAG GAGAACGTGC CTCGGGCCCA GTCACTAGAG GGAAGTGAAG 600 ACAGAGAAGG TGAGGCAGAA AAGTTGGCTC CCCAAGCCCA GGAATCCACA TCTGTGACGA 660 AGTGCTCAGT GTGACAAAGA CTAGGAAGGA AGGGGCCCAG ATGGTGACCT GACCTGGGGA 720 TGCCCACAGC CCTCTGGACA ACACCCTTCC TAGCGCTGGC CCTGGAAGGC ACCCAGCCTC 780 CAGTACTGGG GCTTGTAGAG GGAGCAGCTG TTCAAGCCCC AGTACTTGTC ACAGGGAGCA 840 GTTCAATTCT AGTGGGAGCC CCAGGACCCA ACCAGGAAAC CACAGAGCCG GCAGCCAAAG 900 CTGGTGAGGA CCCACATGCA CCTGGCCCAG CTGGGCAGCC AGGCCCCAGC TCAGCTCCAC 960 AACCCTCCTC TTTCCCTGAA TTTAAGGGAG CGGGGGTGGG GGGGATGGGG GAGGGTTTGT 1020 CAGAGTGAAG ACAAAACCAC AGAGGGTCAC CTTCAGAATC GGCTCACTGT CCCCGACAGC 1080 CTCATGGCGC TGGAGGTCAC AGGAGAGAGT GCCAGGACAC ATGGTGGGGT GTTTTCCGGG 1140 ACAGCGAGCA GAGTGCAGCC AGGTGTGGGA AAGGCGGCAG GGAGGGTATG TGTGGAATTT 1200 AACCTTGTGT CCCCAGTTAG ACTCCATCAA TCCGCACCAG CGCCCTTCAC CCTCATGGGA 1260 GGGGGTGTTC CAACCCAGGA GCCAGAGGTG GCAGAGACTC CGTGGACGTG GCTCACCCAG 1320 GCACGAAGGT GCTGGGCAGT ATGACCCCCG GCTGCAAACT GTGTTACTTC TCAAGATCAG 1380 AAAAAGTGGA GCGCCCTCCC ATTCCATGTA AGGGCCCCCA CCTTTGGCTG TCCCTGATCG 1440 CTGTCCTACA CAATGTGGCA TGGATCTTGG CCAAGGCAAA AATAGTAATT GGCACGGTGA 1500 CAGTGTGATG GGCCAGGCCC AGGCCCCGCC TGCAGGAGCC TGTCATGCTG AGGTGGGCAG 1560 CCCTTCTCAG ATGTCACTGT GCCTGGGCTC ACCTGGGAGC TCGTCAGCCA CTGCATTTCT 1620 GACAAGCCCC CAGGGATCGC 1640
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