| Tag | Content |
|---|
EnhancerAtlas ID | HS147-07582 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr10:126889000-126890700 |
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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I125200 | chr10 | 126889221 | 126891270 |
|
Enhancer Sequence | GAGCTGGGAT CTGAAGTTAC AGCCGAGAGC CTCTTGGAAG GAGCTGGGAG CATCAGGGTG 60
GTGTCTGATG GGAGCTTGAG CTACGTACAG CAGAGGTTCA ATCACTGCCA GAGATGCTGC 120
AGGAAGCACA GAGGGAGGCA GAGACATGCC CGACTCACTC CATCTGCCCT TCAATCCTCC 180
ATCAGTGCCT CCCATTGGCT GAACTCCCTA GAATCCTGGG AACTGCAGTT CTCTGAAACA 240
AGGCAGAGCA GAGAATGGAG CTGAGAGCAA ATGGGCAGTT GACCCTACCC ATCACACTAA 300
GGATGGCATG GCAGAAAGAC AGAGGGCCCT GTGGCTTTAG TGATGATATT GTTAAAACAT 360
GGACAAGTCC ATATCTCACC CGTTGCTGGA TATCTCCTTC TGGGGATGGG AAAAATCTGA 420
AGGCTGGATG TGGTGGCTCA TACCTATAAT TCCAGCGCTT TGGGAGGCTG ATGTGTGAGG 480
ATCACTTGAG CCCAGGAGTT TGAGGTTGCG GTGAGCTATG ATCACACCAC TGCATTACGG 540
ATGGGGCAAC AGAGTGCAAC CCTGTCTCAA AAAAAAAAAA TCTGAATTCA TAAAGCCTCC 600
TGGGCTTGGG CATTTTGTTC TTGTAGGTTA ATGGTCTCAG TGCTGCACCA GGTCTGAGTC 660
AGACCCATGT CTTTCAACTG CCAGTCCTGA GCCTGGGCCA CTGCACCTGC AGACAGTGAC 720
AGAGGCCAGA AACCTGAATC TTTGTCCACT CTGCAGGTGA AGGAGTTCAC TTTGACAGAG 780
CAGAGAAACA GAATGAGTCA GCAGCAGGTC CACACGCTCC TTGTTCTACA ACAGAAAAGC 840
TGCTCTGAGT AACTCATGCA CAGAGTGAGA GAAAGAGGAA GGACCTGGGC AGCCCCCATG 900
ACCAGCCCCC ATGAACCACT GACACGGTTC CACGTCAATG GAACCATGGA CAGAGGTGCC 960
CACGGGGCTA AATCCCAGGT TTTTCCTGGG GCCAATGTGT GAAAGCCGAG AGTTCAGCTG 1020
AATGAGTCAC CTGAGCCTGT GGTTTTTACA CTTTGTTTAG ACTCAGAATC CAAGAACACT 1080
TTGCTCAGAA GCCCAACGTG GGGTTGGGAA CCCCAGGTAT CCCCCTCCAT CCTATCCCCC 1140
AGCCTGTGGG TCTTCCCAGT GCTCTGGAGG CAGTTTGAAA ACAGCTGATC TCAGCCTGGC 1200
CAAGATGGTG AAACCCCGTC TCTACTAAAA ATAAAAATAA AAAAAAAATT AGCCAGGCGT 1260
GGTGGTGGGT GCCTGTAATC TCAGCTATGA GGGAGACTGA GGCAGAGAAT TGCTTGAACC 1320
CAGGAGGCGG AGCTTGCAGT GAGCCGAGAT CGTGCCACTG CACTCCAGCC TGGGCAACAG 1380
AGCGAGACTC TTTCTCAAAA ACAAAACAAA ACAAAACAAA AACCAGCTGA TCTCATCTCC 1440
CTAAGTTAGT TTATAAATGA GGAAACTGAG ACTTCGGTTC TGTTACTTGG TTGCAGTGAC 1500
AGAAACCCTA CTCAAGCTAG CCTGGGTGGC CGGGGGACTT ACTGGCATAG GCAGGGATGG 1560
AGCTGGCCCC AGGGATCAGG GGCATCATCA GCTTGGCAGT TGTTGTCTCT TGTTCCCCTC 1620
CTCACACCCA CACTTCACCC CACATCTGCT GGCTTCTCTG CATGCTGGTG TCGCCACCTC 1680
CTACCGCAGG CCAAATTCTC 1700
|
