Tag | Content |
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EnhancerAtlas ID | HS002-03195 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr14:101539320-101540310 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr14:101539709-101539722 | ATGACATCATTAC | - | 6.48 | JUND(var.2) | MA0492.1 | chr14:101539708-101539723 | AATGACATCATTACC | - | 6.2 | NR2C2 | MA0504.1 | chr14:101539588-101539603 | AGGGGGCAGAGGCCA | + | 6.05 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101070 | chr14 | 101537262 | 101542129 |
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Enhancer Sequence | AGGTTTAACA ACGGAGGCCA TCTGCCTTCA GCAGGGATTC GCACAGAATG TCACTGGCCT 60 TCGCCCAACA AGCACTTTGC AGGGAGCAAC CTCCTGAAGT CGGGGCTCAC TCCTGGGTCC 120 CCCTCCACTG CATGCGAGCC CCCCGTTCCA AGGCAGGAGC CAGGGTCACG AAAATGCATG 180 CTTCTTCATC AATCCGAGGT CTCAAACGGC TCCCCCAGCC CCACTGCCTG CCCGTTCCAG 240 GCCTGGGGCT GGCAGCCTGG GCCCCACGAG GGGGCAGAGG CCAGAGCCCG GCGGCAGAGC 300 CCGTGCCCAC GCCTCGCTGC TGCCAGCCTC CGCTTGGTCA CGACACAGCC AGGCTGACTC 360 AGACACAGCC CCAAGCGGGA GCCTCATAAA TGACATCATT ACCTATGAAA CCTGCCGTGT 420 AGTGCGCTAG CAGGGAAGGA CACACTCTGG CCGCCCGGTG ACTCACACTG TTTTCCCCAG 480 AGCCTTCCTG CTCCACCGCC TGGGTCTGAG CTGGCTGGGC AGGGGGAGGG GGCACTCAGC 540 TTGGCCTCAC TCCCCCGCTC TGCTGCAAAT GCAAAAGCAA TCGGCCAGGC AGCCACCATC 600 CTGCTGAGGG CTGTGTGTGG GGGTGGCGGG GAGGAGGGGG GGCACCATCT CTCCGGCCTC 660 CCTCTGCAGC CCCAGTGGCG CTCCAGAGGG ACTGTCAGTT GCCTATGACA GGGGAGGAAA 720 CTGAGGCCTA AAGAGGCCCA ATGCCTGGCC TCACAGATCC CACAGGGGAG GGTGGCTTCG 780 GCTCATGCTG GGAACCCCCA GGGAGACCCT TCGGCGAACC CAGCCGCTGG GCAAAGCTGC 840 AAAACCTCTG GCTGTTCCTG CTGGGCCTGA GACTCCAGCT TCTCCTGAGC TCCTTTGGTG 900 CAGCCAACTC CTCCTGCTGA AAAACACTTC TACTCTTGAA AGTGGTGGCC TTGCCAACCC 960 AAGATGTCCC CACCAGGTGG GGGGCACTGT 990
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