Tag | Content |
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EnhancerAtlas ID | HS133-11897 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:84569920-84572480 |
Target genes | Number: 14 | 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 | chr16:84571477-84571495 | TCTTCTTCGCTTCCTTCC | - | 6.22 | Mafb | MA0117.2 | chr16:84570915-84570927 | AGTCAGCAGTTT | - | 6.22 | SOX10 | MA0442.2 | chr16:84571193-84571204 | AAAACAAAGCA | + | 6.02 | STAT1 | MA0137.3 | chr16:84570951-84570962 | TTTCCAGGAAA | + | 6.62 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I084536 | chr16 | 84569823 | 84572575 |
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Enhancer Sequence | AGACAACATA GCCATTTCAA TGCCTTTCCT TCACACGGGA AGGCCACCTT TCCAAACAGG 60 ACAGTCTTGC TCAAGGTTCT TTTGGTTGCA GCCGACATAA ACCCACGGCG GCCTCCACGG 120 GCACGCAAGC TACCAGCCGC ACAGGCTCGC ATTCAGAATG GCTTCATGCT TTGTTTCGGG 180 TTCTGCTGCT GCCATATTGA AATTCTTAAC ACATTTTGAA CAAAAGGCCC CACCATTTCC 240 TTTTGCATTA AGCCTCTAAG TTCTGTAGTT GGCCCTGCAT AAAGCCATTC TGGTAACTTG 300 GATTACCAAG GGGAGATTTA CGAGAAGGAC AAGGGGTGTC TCTCAGAACC CAAAGGTGAG 360 AACTGGAAGC AGGGCCTGGA AAACCAGAGT CCAGGAGGCC GGTACTCGCT CACAGTCTCT 420 CTCTCCCTCT GTCTCTACTT GTGCTTCATT TGTCTTATTC TGTTTTTTTT TTTTTTTTTT 480 TTTTTTTTTT TTAGATGATG TCTTGCTCTG TCGCCCAGGC TGCAATGCAG TAGCGTGATC 540 TCGGCTCACT GCAACCTCCG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCATCCCGA 600 GTAGCTGGGA CTACAGGCAC ACACCACCAT GCTCGATCAA TTTTTGTATT TTTAGTAGAG 660 ATGGGGTTTC ACCATGTTGG CCAGGCTGAT CTCGAACTCC TGACCTCAGG TGATCCGCCC 720 ACCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCGTGCCTG GCCCATTTCT 780 GTCTTATTTT CTCTCTGAGA GAGACAACAC GGCTGCTGGC CCCACCCAAG ACTCCATCTC 840 CTTTGTCCCA GATATCAGAC CCAATGGCAA TTTCATGAGA CAGAGACTCT GATTAGCCCA 900 GCTTGGGTCA GGTGTCCAGC CCTGGTCCAA TCAGCTCCAC CCCACGGGGC AGGGTCCCAT 960 AGTGCCAACA GGGCGCCCAT ATGGAAGCAG GAAACAGTCA GCAGTTTGCA AAAAACAGAT 1020 TCGCCTTGAA GTTTCCAGGA AACACATTTA GCCAGGCCCC ACCCCACCCG CTGCAGCAGC 1080 CCCAGACTCA CTGCCCAGCC ATCTCATGCT GACTATCCTA TGGGCGCCCC TTCTAGAAAT 1140 GCCCTCAAAA TGTGTTTGGT GATTGATTAA TTGACCATTG GCCTCAAGCC CATTTCTAGC 1200 TGAGCTATTG ACTTTTGTGC TGGGGGTTTA GAGAAAATCC TATCCTCTAT TGTCATTTTC 1260 TTTCTCCTGT TTAAAAACAA AGCAAAGCAA ACAAACAAAA CTCCTTCACA AGGAGGCTGG 1320 GAGGGCGCAC AATATAGACA GCTGTGAAAA AGGCTGGTGT GGGGAGAAGC TTCTCTCTCT 1380 CTCTCCATGC ACACAATGTA TATTATCTAA GGCTGTGTCA GCAAGCTATA TATCTTTGAC 1440 CCTTCAAAGT CTGGCTCTTT GTAACTCATT GCAAAGAATT CTCTTGGGGG CACTCAGTTC 1500 TGTGAGGGAC AGATAGCCGC CTCTCCCAAG GAAGCGGATT CGACTCTGGG AGATAAATCT 1560 TCTTCGCTTC CTTCCTCTCT GAGACGATTA TGAAGAAAGT GCTCCCATAG TCCTGGCAGG 1620 AACAAAGGCC CTGTGTCCAG AGAGGCTCCC CCACCCGACC TCTCATGCAT TATGAATGGG 1680 GCCTCAAGAT CATTTCACAA GCTTTTCACG CTCCGAAATG GCCACTCCCC AGCCTTAGGC 1740 TGCCCAGCTG TCGGAGACCC CTTGGCCCCT TCAGGGCTAT GTCCCCCATG GCTCCTTCAC 1800 GCCAGCCCCA GGGGACTGAC AACCTCTCAG CCATAAATGT CAGCCAGGCC TTCTGCCGAT 1860 GCCACCGGGG GATGCGGAGG GTAATCGGGA CATGCTCTGT TGTCCCATCA GTAAAATTAT 1920 TAGGAATTTC AAAGAATTAA ATCCCAAGCA CAGGCCCTTC TGAGTGCAGG GCCCTTGGCT 1980 GCTGCCCTGG GAGATAATTA CCCACGAGAC TGGCCCTGAC TGTAGCTATA ATTTCAACTT 2040 ATCCATCACC CTGATTCTTT GACTCAGGAA AGTTATTCAT TAAATAAATA TTTTTCTAAG 2100 AATTTCAGAG CATCCACTAA AGCAGACCAT AGATCTGCAC CATAACCCAG CATTTTCACT 2160 GTGTATACAC CCAGAAGGGG GATGTGTGTG GATAAGGAGT TGAACTAGAA TGTTCTTTGC 2220 AACACTGTTC ACAATAGCCC CACATTGGAA ACCACCCAAA TGCCCATCAA TAGTAGAATG 2280 GCTAAATAAA TGTGGTCTGT CCAAGTGATG GAAAACCACA CAGAAAGAAG AATGGCTTCA 2340 AACTACACAC AATATGGCCG ACTCTCACAA ACAATACGGA ATGAAAGAAG CCAGACACAA 2400 CAGCGTACAC AGCATATGGT TCTGTGCTGT TGGAAGTTCG AGTCACGCTT ACTGTTGAGG 2460 GTGACTCAAT AGGGGGCATG AAGTGGGGCT TGGGGGCTGA CACTAGTGTG TTATTGACCT 2520 GAATGCCATT GCATGGTTGT GCTTAGTGTG TGAGTGTTCT 2560
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