Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151993750-151993988 | Common:4; Rare:85 | ||||
chr1:153633851-153634103 | Common:4; Rare:78 | ||||
chr1:153727763-153728097 | Common:1; Rare:101 | ||||
chr1:153963477-153963698 | Common:2; Rare:58 | ||||
chr1:153967619-153967945 | Common:1; Rare:57 | ||||
chr1:153986207-153986418 | Rare:56 | ||||
chr1:154172914-154173157 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182986-154183277 | Rare:93 | ||||
chr1:154220519-154220973 | Common:1; Rare:154 | ||||
chr1:154627881-154628005 | Common:3; Rare:65 | ||||
chr1:154970693-154970869 | Rare:33 | ||||
chr1:154974337-154974738 | Rare:105 | ||||
chr1:154983097-154983418 | Common:2; Rare:67; Clinvar (benign):2 | ||||
chr1:155135710-155135903 | Common:3; Rare:82 | ||||
chr1:155173831-155173873 | Rare:8 |