Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151763326-151763624 | Common:3; Rare:130 | ||||
chr1:151790470-151790885 | Common:3; Rare:98 | ||||
chr1:153535933-153536088 | Common:1; Rare:35 | ||||
chr1:153545756-153545863 | Rare:18 | ||||
chr1:153609344-153609467 | Common:2; Rare:18 | ||||
chr1:153628236-153628494 | Common:1; Rare:59 | ||||
chr1:153633974-153634153 | Common:1; Rare:54 | ||||
chr1:153658868-153659008 | Rare:53 | ||||
chr1:153670916-153671247 | Rare:112 | ||||
chr1:153963504-153963697 | Common:1; Rare:50 | ||||
chr1:153967306-153967508 | Common:1; Rare:40 | ||||
chr1:153967624-153967908 | Common:1; Rare:52 | ||||
chr1:154172906-154173203 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182986-154183035 | Rare:14 | ||||
chr1:154220340-154220399 | Rare:17 |