Tag | Content |
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EnhancerAtlas ID | HS179-10066 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr12:132673770-132675850 |
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) |
KLF5 | MA0599.1 | chr12:132674180-132674190 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr12:132674249-132674259 | GGGGCGGGGC | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I132190 | chr12 | 132675528 | 132676831 |
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Enhancer Sequence | GTGCCTCCGG GGTCTGTCTC CCGGCATTTT TCATATTCCA CGGGGTTCTG TCATCCTGAC 60 TGTGAAGGGC ACACGGAGCC GGGTCCTGGC CCATTTGACC GGCTCGGCTC ACCCCTGCGC 120 TGCCTGTTCG CCTGTGTCCG TCTGTCCGTC CATCTGTCTG CTGGCCACAG CTCTTCCACC 180 CTCGGGGAGG TGTTCTTCCC CCTCTGCTGA GCCTGCATGA AGACGCGTGC GCTCAGGCCG 240 GCGTCTGCAG TGTAGACACA GCTGCCTAGG CTCACTTGTG GTGTGGACGC TGTGCTGTGC 300 CGGTGTTGCG CTGTGTCCGG TGCAGGCGCC GTCCTCTGGC TTCTCTGGGG TGTGTGCAGC 360 GTCGACGCTG TCCCGGCGGG GCTCGGAGGG AACCGCCCGG CGTAGTGTGA GGGGCGGGGC 420 CGCTCCTGCG GAGTCCACGG AGCTCGGCCG GCCGCGGGGG CCTCTTCGCC GAGGGAGTCG 480 GGGCGGGGCC CGTCTTTCCG GGGACGGAGC ACGGAGGAGA CGCAGCGACG GAGGAGTCGA 540 GGGCGGGGCC TGGGGCGGCC CTTCGCCCTT TTAAGTCACT GCGCGCGGGT CCCAGGCGGC 600 GCCCGTCTCG GGGGCAGGTC CGCGGGGTGT GACGAATGTT CCCGCGGCGT CTCCCCGCCC 660 TCCCCGGCGC CTCCCCCGGC CTCGGGCAGC CGCTTTCTGC ACGGCACCTC CGAAGCCGCT 720 GGGCGTCTGT AACCAACCTG CACGTTGTGC GCATGTGCCC CAGAAATTAA AGTAGAATAA 780 ACAACAACAA AACCAAAAGA CCTTTTTACT TTGACGCAGT TTTAGATTCC CAGGACGTTG 840 CACAGAAAAT CCGGACGGAT CCTGTGCCCT CCGCCCAGCT CCCGGGGTCA CAGGCAGCCT 900 CGGCTCCGAC CCCGCCGGGC GCGCGGTGAC CGGCTGTGCG GGTTCCAGGG GCGGATGTGC 960 GCTTTGCCCG GCCCCTCTCC CGCCGCGCGG CCGCTCCTCC TCTCCGCCAA GGGCCGGTTC 1020 AGGCACAGGC CCCGCCGAGG CTGCCCCTGA CTTGAGGGCT CACGCACCGG GCTGCTTGCG 1080 GCTCTGGACT ATTGTGAATA AGGCCGGTGT GAGTATTTTA CTGTAAGTCT TTGGGGACGT 1140 GTCTTCATGC CCCTTGGGTG AATCCAGGTG TGAGATTGCC GGGCCGGGGT GCTGTGAGTT 1200 ACCTTTGGTT ATAGGGAGGT GGTGACCCAT GGTGGCTCCA AGTGCCCGTG GCCTTTCGTG 1260 ACCCCGCCAG CAGCGGGTGG GCCTTTGGGG CGCTCCGAGG CTCGCCCGTG CTGCCCGTGG 1320 GTGCTTCAGC CAGTCCGGCC GCCGTGGCTT TCCTCTGCAG CCCCCGGTGC CTGCTGGCGT 1380 CGTGCCTTTC CGTGTGCTCG TTGGCCACGC ACATGTCGAG GGGCCGTTCT GACGATGGAC 1440 TGAGGGGCTC GGGGATAGCA CGTGTCCAGC GGGGCAGGTC AGCCTTTCTC TTCTCCCCAC 1500 AGACCTCAGC ACAGCTCTGC ACCTCGGAGG ACTCGGGGAA GTTTCTGGGC CTATTTGGGC 1560 AATAGGAGAA GGTCATGGGC TGTCTTTCCA AAATTCACGT CCACCCAGAA CCCCCGAATG 1620 AGACCTATTT AAAGAGAAGG CCTTAGCTGA TGGAACATTA AGATGAGGCC ACCCTGGAGC 1680 AGGGTGGGCC CTGAATCCGA GGCTGCTGTC CCTGCAAGGT GACGAGAGGG TGCAGGCGTG 1740 GAGGAGACAC ATGGGGGTGG GGTGAGGAAC AGGCCACCGG CAGCAGAGAC GGGTCAGGCC 1800 CAGCGAGGGA GGAGGTGGGA GGAGCCCCGG AGCCCTCGGA GGAAGCCGGG CTGGCACCTG 1860 GGCCTTGGAC TCTGGGACTG TGAGGGAATC AATTCTGCCA TCTGAAGCCA CCTGCTGTGG 1920 TCCTGTGTTA CAGCAGCGCT GGGCACAAAC ATGGGAGGGC CTCGTGATTG GGACTGGGGC 1980 ATTCACAGGC CCGGCAGGCT GGTGAGCCGG TGCCTGGCAG GTGGGGAGGA CATGGTGTGA 2040 GAGGCGGCCT GCGGGCCGGC CAGTGAGCTC CAGCACGGGG 2080
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