Tag | Content |
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EnhancerAtlas ID | HS133-11130 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:24620890-24622490 |
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 | chr16:24622060-24622081 | CTCTCTCTATCTTACTCCTCC | - | 6 |
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| Number: 2 | ID | Chromosome | Start | End |
GH16I024609 | chr16 | 24621122 | 24621330 | GH16I024610 | chr16 | 24621481 | 24622121 |
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Enhancer Sequence | GAGAGAGAGA GAGACAGAGA GAGAGAGAGA GAGAGAGACA GAAGGGAAAT ATCTGCAGAG 60 AGAACAGAGC TATGATCACT AAGTAGAACA GAGGCAGCCT AATCGCCTAA TCAGATACCC 120 AGTCGGGGCC CCACCTGACT CCTACTGCAG CTGGGGGGTG GAGGGACTAG AAGGTTCAGC 180 TGGAGTGGTC TCCCCTTCTG CAGCTCCAGT CTCCCCACCT CCAACCCCCA CTGCCACTGC 240 CCCGTGAGGA GGCTTGGAAG CTGTGGGGAG GGGAGGCAGC CGAGTTGGGC TTCTAGAACG 300 AGGCGGGATG GTGTGAGCTC AAACGCCCTG CAATTGCTGG AGCAACAGCG GCGACACTTG 360 AGTTATTCAC AAAGGCTGGA ATTCAAATGA GGCTGGCACC GCTCCAAGTC GCAATAGCTT 420 AGGAGGAGAG AGAAAGGCAT ATTAACTATT CATCAAGGTC TTCGCGTTGC ATGGGCTCTG 480 AGGGTTCTCC ATCTGCGTCC CTCCCTCTGT CACTGACTGG GGGTAGGGGG CGGGGGGTCC 540 CCCAGAAGCA CTTTATCTGT CAGTCTGTGA GCGGGGGCTG GGGGTGGGGG ACTGAAGTTA 600 GGCAGATTTG TCTCATCACA TGATGGGGGA CCTGTATCAT GTGATGGCTC CGGTGATGTT 660 GGAGGCGGCA TGTGACTCCC AGGGCTACGT GGGTTCAAAA ACAATTTAAT ACAAAAACAC 720 AAGCAGGTTC CCCTCCTCTC CTTTGCCTTT GGTCTGGCTC TCCCCATCGC TGGGTTCAGT 780 GCCTGACTGA ATGGAAAACC CGTCGTCTTG CAGCCACTAA CCTGTGAGCG CCGGGTACCT 840 GGAGACCAGG CCCCTCTGCT GGGGGCCCCC AGGAGCGGTG CCCCATCATT TTGCAGCCCA 900 CTGACTCCCA GCCTGGTAAG TTACTGCACA CTTTCAGCAA TTATCTGCGA AGCTTTCCTC 960 AACTGCCTCA TTAGCATGCG CAGGGCACCC TCGCTGGGCC CGTTGGAAGG GAAGTGCCTG 1020 CCGGCTCTGG GGAGCTGCGG CTCTCGGGCC CTGCCAAACA GACGCAGCCT TCCTAAGGAG 1080 CAGCGCTGCG CTGGCTCTGC TGGGGTGGAA GGAGCTTCTC CTTCGCTGTC CTCCCTCTCC 1140 CTTCCCAGCC CATCTTATTC CGAGCCTCTC CTCTCTCTAT CTTACTCCTC CTAACCTCTC 1200 TCACCTCTCA CCTTCCCCCT TTCCACCCCC TGCCCTCAGA TTTATTTATT TATTTATTTA 1260 TGACAGAATC TCGCTCCGTC GCCCAGGCTG GAGTGCAGTG GCGCAATCTC GGCTCGCTGC 1320 AACCTCTGCC TTCCGGGTTC AAGCGATTCT CCTGTCTCAG CCTCCCGAAT AGCTGGGATT 1380 AGAGGCGCCC ACCGCCACAC CCGTCTAATT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC 1440 ACCATGTTGG CCAGGCTGGT TTCGAACTCC TGACCTCCGG TGATCTCCCC GCCTTGGCCT 1500 CCGAAAGAGC TGGGATTACA GGCATCAACC CCTGAGTCCA GCTGGATTTT CTTTTTTATT 1560 CACATACCTT TCTGTCTCCC ACTGATTTTT CTTAGGAGTT 1600
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