Tag | Content |
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EnhancerAtlas ID | HS060-10851 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:103039810-103040510 |
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 | chr14:103040352-103040373 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | MEF2A | MA0052.3 | chr14:103039829-103039841 | TTTATTTTTAGA | - | 6.07 | SPI1 | MA0080.4 | chr14:103040052-103040066 | AGAAAGAGGAAGTG | + | 6.51 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I102573 | chr14 | 103039803 | 103042777 |
|
Enhancer Sequence | TTTTTTTTTT TCAATTGACT TTATTTTTAG AGCAGTTTTA GGTTCACAGC AAAATTAAGT 60 GGAGGGTACA GAGAGCTCCC GTCCACCCTC CTGTGCTCAT TTTGTAATGG TGCAACAGCA 120 CAAAAGTCTG GTCATGGATG CTAGCTTCAT GCCCATCACA GGTGGCAGTG AGTGCTCCTG 180 CTCCAAACGT CCTCACTCCG GGACACACGC TGATGAAGTT TCTCTTCTAT GGCATGGGGA 240 AGAGAAAGAG GAAGTGGCAG GTTCCCCACT GACTATTTAA GCCTTCAGCC AGAGATAACA 300 GGTCACCTCT ACTCACATTT TAGTCGCAAA GCAAGTCATT CAGCAATTCC TAACTTTAAG 360 GGGGTGTGAA ATTCTCCCGT GATCCTGGAG GAGAGGGTCT GAATATATGT GGCCACCCCT 420 AAAGACTCAC GGGAGTTAAA TAAGGTTCTT TTGTGCAGGA CTTGTCACTG CATTTCCTGG 480 GCCACCTGGC AGGTGGCAGG TGGAGTAGCG CCGACATACT TGACTGGGGA ACCCTTCTCT 540 TTTTTTTCTT TCTTTTTTTT TTTGAGATGG AGTATCGCTC TGTCACCTAG GCTGGAGTGC 600 AGTGGCGCGA TCTCGGCTCA CTGCACCTCT GCCTTCTGGG TTCAAGCGAT TCTCCTGCCT 660 CGGCCTCCTG AGTAGCTGGG ATTACAGGCG CGCGCCACCA 700
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