| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161749608-161749850 | Rare:81 | ||||
| chr1:161766125-161766546 | Common:5; Rare:123; Clinvar (pathogenic):1 | ||||
| chr1:162023625-162023969 | Common:1; Rare:98 | ||||
| chr1:162497756-162497867 | Common:1; Rare:41 | ||||
| chr1:162561346-162561734 | Common:4; Rare:148 | ||||
| chr1:162631093-162631377 | Common:5; Rare:55 | ||||
| chr1:162632256-162632563 | Rare:60 | ||||
| chr1:162790447-162790781 | Common:4; Rare:87 | ||||
| chr1:163202854-163203054 | Rare:36 | ||||
| chr1:163321706-163322013 | Common:1; Rare:82 | ||||
| chr1:164558917-164559185 | Common:1; Rare:74 | ||||
| chr1:164590134-164590375 | Common:3; Rare:54 | ||||
| chr1:165630791-165630910 | Common:1; Rare:39 | ||||
| chr1:165698367-165698633 | Common:2; Rare:128 | ||||
| chr1:165768690-165769055 | Common:2; Rare:138; Clinvar:1 |