| Tag | Content |
|---|
EnhancerAtlas ID | HS040-05405 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr10:122999520-123000550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr10:122999809-122999824 | TGCCCTCTGACCCCC | - | 7.23 | | RREB1 | MA0073.1 | chr10:122999947-122999967 | CCCCCAACCACCACTACCGA | + | 6.71 | | ZNF263 | MA0528.1 | chr10:123000443-123000464 | TCCCCTTCATTTTTCTCCTTC | - | 6.33 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I121239 | chr10 | 122998915 | 123000601 |
|
Enhancer Sequence | CCCAGAGAAG GCAGTTTCTT TTTGGGCCAG TGGTCACTGA CCCTCAGGCA GGGGCTCTCA 60
GTATACAGGG TCTGCTGGCC CTAGCCCCTG ACACTCTACC TAGTGACCCT TGCCCCATGG 120
CCAGCTGGCC TGTAGAAGGA AGTCACAACT CTGGCAGAGG CTCAAGGCGG CAGCCGGGCT 180
TCTTTGTGGC TGCCTTCTCT CCCAGCTCCA CCCCAGTGTC TTCTGACTCA CCCCAACTCC 240
CTAGAGCAAA GAGCTCTCCT CCATAACTCA GAACCCCATG ACTGGGAGGT GCCCTCTGAC 300
CCCCTCTTAT TCTGCAGCTC ATTGGAACCT CTCCCTGCTC AGGAGACCGG ACCTCCACTC 360
TTCCCAAATC ACGGTCAGGC CTGTCATCCT GGATACCCTT TCCTGTAGGT AGACTTTCTC 420
CCATTCGCCC CCAACCACCA CTACCGAGAT GGGAAGTAGG AGGGGTTCAG CACCCAGCAA 480
CACCCTTGGA TTTAGACCTC AATTTTGGAA AGTTCCTTAT TGCAACTAAA CCCCTCACCT 540
TAATCCCCTC CTAGACCCTG CCCCTCCTGG TACCTGCCAC GTGTCAAAAG ACAGCATTTA 600
TTCTCCTGTT TGTCTTTTCA CCCTGATTTG CTGTGTGGCC TTTTCCTTGT TATTAAATAA 660
CCAGGATATG TATTTGTTTT GCTCTGGCTG AAGAGTATGA CACACATAAC AAAACAATAA 720
AAGCACCAAA GAGCACCTGT TACCTTTCCT GCCCAACCAT GCTTAACTAT ATTGCCCACA 780
CATTCAAGGA ATGATCATCT TGTCCAGATA TGACAGCATC TGGCCCTTGG CGCTTATCTG 840
CCTTTATGGA TCCTTTTCTG TTGCTTGCCA CCTACCAGCT TCCTTTATCA ATACCAGGAA 900
GCTCTCTACA CATCCTTCTG TGTTCCCCTT CATTTTTCTC CTTCACCAAT GCACTTTATA 960
AGGAAGGTAA ATGCCTCAAA AGTCTTGTGG AAAAAGCTGT GTAGGAATCC AAATCTCCAT 1020
TTTGCAGACA 1030
|
