Tag | Content |
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EnhancerAtlas ID | HS113-05467 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr10:114751080-114752690 |
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) |
IRF1 | MA0050.2 | chr10:114752517-114752538 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | IRF1 | MA0050.2 | chr10:114751266-114751287 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | MYC | MA0147.3 | chr10:114751555-114751567 | GGGCACGTGGGG | - | 6.07 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I112991 | chr10 | 114751297 | 114752537 |
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Enhancer Sequence | GATCGAAACC ATCCTGGCTA ACACGATGAA ACCCCGTCTC TATGTGCGTG GTGGCTGGCA 60 CCTGTAGTCC CAGCTGCTCG GGAGTCTGAG GCAGGAGAAT GGCGTGAACC CGGGAGGCGG 120 AGCTTGCAGT GAGCCGAGAT CGCCCCACTG CACTCCAGCC TGGGCGACAG AGCGAGACTC 180 CATCTCAAAA AAAAAAAGAA AGAAAAAAAA AGAAAGTGGG GAACCCCTCC CCCAGGATGA 240 GAAGAGCCAT GGGGTGAGTC TCTGCCACCG CCAAGGGGAG TCAGGCTCAG AGGCTGCTAC 300 AGGGACAGCC AGCTCTCTTT AGATGGTCCC CACCATCTAG TCAGGGCTTG TTACATATGG 360 AGCAGAGACA GCGCAGGCTG CTGCTGTTTT CCTGGAGAAG GCCCCTGTCG GTCTGTTCAG 420 CTGTAGCTGA CCTTTCCTCC TTGTGCTTTT TGGGGAGGGA GCCTTGGAAG GAGTAGGGCA 480 CGTGGGGCAC TCTGCTTCCC GGCCCCACAC TGGCGAACCT ATGGATTCTG CCTCTGATTC 540 CTGAGGAAAC ATCACTGTGA AGGTGGAATG AGCCACATAC AGAGGTGGCT GTTGGGGCCG 600 GGGAGGGGTG AAACGCCCCC AGGGTGTACA TTGCACCAAA AGCCAGGCTG CATATAGACC 660 TCAGGATGGG CTGGCTTTTC TATTTATTTA GAAGTATTTC CAGAGGGTAA CCTCATTGGC 720 TACAAAGCAT GTCTGAACAA GAGCTCCGTT GTTCATTCCC AGCCCTGTTA CCCTGGCAGG 780 ATGCAGACTC CAGGCGGCCT GTTGGTCAGG CCTTGGACTC AGAGAGCAGT GAAGCCTGAG 840 GAGGGGTGGG GGGCAGAGGC GTGAGTGGTC TAGGGCCTCA GTCCCTCCAG GACACCCCTT 900 GCCAAGCGCA GAGAAAGCTC TGCCCATCCG TCCCCTCAGG CAGTGGGATT GGGCAACCTG 960 GGAAGCAGTG AATGTGCGTC GGTAGCATAG ATTCCATTCC GCACGCCACC CTCGCCTCCG 1020 CCCCCCAGCC CTGGGAGGGA TGCATGCCCT CCGGGAGACA CCCAGACCCG ACAGAGAGGC 1080 CTTTGTTGGA GCTGGAGGTG AGAATCTGTG GGCGTTGGGA TTCCTGGGTT CGAGTTCCAG 1140 CTCACTGCCA ATTGCCCGAG TGCTGGGCGA ACATTTCTGG AATCAAAAGG AGTGCAGCCT 1200 GCCCAGCAGG GCCTACGGGA GCCGGAGGCT GCAGGGTGCT AAGATTGCGT TATCTTTACC 1260 AAGTGCCCGG AGCTCCTGGG AGGGAAGAGA GAGTCCTAGG ACTCAGGATA GGAGGTGGTT 1320 GGAGTTTCTC GAGGAAGACT CCATGCTTTG GTTCTGGCCC CTGGAAACCC CTCCTGAGGA 1380 CTGGACCTCC AAGCAGACCC CCTCTGTGAC TCCGGAATGC AGTGTTACTC TCTTATATTT 1440 TTCTTTCTTT TTTTTTTTTT GAGACGGAGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT 1500 GGCACGATCT CGGCTCACTG CAACCTCCGC CCTCCGAGTT CAAGCGATTC TCCTGCCTCA 1560 GCCTCCCAAG TAGCTGGGAT TACAGGTGCC TGACACCGCG CCTGGCTAAT 1610
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