Tag | Content |
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EnhancerAtlas ID | HS060-04910 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:126889530-126890200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr10:126890020-126890031 | AATGAGTCACC | - | 6.02 | Nfe2l2 | MA0150.2 | chr10:126889788-126889803 | CAGAATGAGTCAGCA | + | 7.26 | TFAP4 | MA0691.1 | chr10:126890179-126890189 | AACAGCTGAT | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I125200 | chr10 | 126889221 | 126891270 |
|
Enhancer Sequence | TGCATTACGG ATGGGGCAAC AGAGTGCAAC CCTGTCTCAA AAAAAAAAAA TCTGAATTCA 60 TAAAGCCTCC TGGGCTTGGG CATTTTGTTC TTGTAGGTTA ATGGTCTCAG TGCTGCACCA 120 GGTCTGAGTC AGACCCATGT CTTTCAACTG CCAGTCCTGA GCCTGGGCCA CTGCACCTGC 180 AGACAGTGAC AGAGGCCAGA AACCTGAATC TTTGTCCACT CTGCAGGTGA AGGAGTTCAC 240 TTTGACAGAG CAGAGAAACA GAATGAGTCA GCAGCAGGTC CACACGCTCC TTGTTCTACA 300 ACAGAAAAGC TGCTCTGAGT AACTCATGCA CAGAGTGAGA GAAAGAGGAA GGACCTGGGC 360 AGCCCCCATG ACCAGCCCCC ATGAACCACT GACACGGTTC CACGTCAATG GAACCATGGA 420 CAGAGGTGCC CACGGGGCTA AATCCCAGGT TTTTCCTGGG GCCAATGTGT GAAAGCCGAG 480 AGTTCAGCTG AATGAGTCAC CTGAGCCTGT GGTTTTTACA CTTTGTTTAG ACTCAGAATC 540 CAAGAACACT TTGCTCAGAA GCCCAACGTG GGGTTGGGAA CCCCAGGTAT CCCCCTCCAT 600 CCTATCCCCC AGCCTGTGGG TCTTCCCAGT GCTCTGGAGG CAGTTTGAAA ACAGCTGATC 660 TCAGCCTGGC 670
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