Tag | Content |
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EnhancerAtlas ID | HS133-23751 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:6728430-6729350 |
Target genes | |
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) |
ZNF263 | MA0528.1 | chr4:6728662-6728683 | GGAGGAGGAGAGAAGGAAGAC | + | 6.29 | ZNF263 | MA0528.1 | chr4:6728659-6728680 | GGGGGAGGAGGAGAGAAGGAA | + | 6.94 |
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| Number: 2 | ID | Chromosome | Start | End |
GH04I006727 | chr4 | 6728901 | 6729050 | GH04I006728 | chr4 | 6729081 | 6729328 |
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Enhancer Sequence | TGAGCCACCA CATCCAGCCT CCTGTACCAT TATTTTACTA GCTGTGAATT TGGGCAAGTT 60 ACTGGTGCTC TCTGACCCTC AGTCTTTTTA TCTGCAGAAT GGGGTTACTC AAGGCACCTA 120 CTTTCTGAAA TTGTTGGAGA GTCCTTGAGC TCAGGGGGCG AGGAGGACAG AGTTTTGTGA 180 GGCACTATTC ACCTTTCAGT GGAAACATTT TTAATTTTGT TTCTGTCCTG GGGGAGGAGG 240 AGAGAAGGAA GACTGGGGGT AAGTTCTCCC ACGTAAGACA GCTTCCTATG GACGATGAAT 300 TTAGACTCGC CGCATCTGTG CATGCTCGTG TGGCCTCCCA GAGCCCGGGT GGCAGATGGG 360 TGGCCTGGCG TGAGCATTCT TCGTTTCAGG CTGTGCCGGG CCTCCCCTTA ATAAAGACCT 420 GTTTCTTCCC GGCTGCACTC TTGGCCCAGC CACCAAGGCT CAATGAGCTA TTCTGAGCTC 480 CCGGCCTGCC CGCCGTGGAC ACACTCGGGC CTTCTGTTTG CCCACGGCCG CCCTGTGGGG 540 CTTTCATAAA GCAGCCCTGT TCTCTCTCCC ACCGCGCAGC CGCCTGCTCC TTGGGGCCTT 600 CTTAGGGAGG AGGCCGTGCC AGCCCGGGAG CCGGGGGCGT GGGGAGGCTG CGCTTTGCTG 660 GCTTCCAGGA AGACGCACAC GCTGTGTGTG GCCAGAGACC GGGGCACCTC TTTGTTGGCG 720 GCCCCATTGA CTTAGGGGCG ATTTGTTAGG GGTAAGACAC GTGTTCGGCG AGCAGGCTGC 780 TGCTGCTCAC TCCCTTGAGA GAGGGCAGGC CTCCCTCTGG GATGCACGCT CACCAAGGCC 840 ACAGGGTGCC GGGCCTTTGC ACGAGCTGTT CCTCTGATCT TCCTGGGGTG GCCTCCTCCT 900 CGTTCCCCCA CTCCCCTCCT 920
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