| Tag | Content |
|---|
EnhancerAtlas ID | HS147-07471 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr10:122999390-123000210 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr10:122999488-122999498 | ACCACTTGAA | + | 6.02 | | NR2C2 | MA0504.1 | chr10:122999809-122999824 | TGCCCTCTGACCCCC | - | 7.23 | | RREB1 | MA0073.1 | chr10:122999947-122999967 | CCCCCAACCACCACTACCGA | + | 6.71 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I121239 | chr10 | 122998915 | 123000601 |
|
Enhancer Sequence | CTCCACTAGT AGGAGTTTGG GGCAGTTGAA GTATAACTCT TCTATTTTCA AATTCATCCA 60
AATCACAGAA CAAGAAAAAA AAAAAAAAAC CTAACCAAAC CACTTGAAAG AAAAAAAAAA 120
AAAACAGTTC CCCAGAGAAG GCAGTTTCTT TTTGGGCCAG TGGTCACTGA CCCTCAGGCA 180
GGGGCTCTCA GTATACAGGG TCTGCTGGCC CTAGCCCCTG ACACTCTACC TAGTGACCCT 240
TGCCCCATGG CCAGCTGGCC TGTAGAAGGA AGTCACAACT CTGGCAGAGG CTCAAGGCGG 300
CAGCCGGGCT TCTTTGTGGC TGCCTTCTCT CCCAGCTCCA CCCCAGTGTC TTCTGACTCA 360
CCCCAACTCC CTAGAGCAAA GAGCTCTCCT CCATAACTCA GAACCCCATG ACTGGGAGGT 420
GCCCTCTGAC CCCCTCTTAT TCTGCAGCTC ATTGGAACCT CTCCCTGCTC AGGAGACCGG 480
ACCTCCACTC TTCCCAAATC ACGGTCAGGC CTGTCATCCT GGATACCCTT TCCTGTAGGT 540
AGACTTTCTC CCATTCGCCC CCAACCACCA CTACCGAGAT GGGAAGTAGG AGGGGTTCAG 600
CACCCAGCAA CACCCTTGGA TTTAGACCTC AATTTTGGAA AGTTCCTTAT TGCAACTAAA 660
CCCCTCACCT TAATCCCCTC CTAGACCCTG CCCCTCCTGG TACCTGCCAC GTGTCAAAAG 720
ACAGCATTTA TTCTCCTGTT TGTCTTTTCA CCCTGATTTG CTGTGTGGCC TTTTCCTTGT 780
TATTAAATAA CCAGGATATG TATTTGTTTT GCTCTGGCTG 820
|
