| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:232805318-232805425 | Common:2; Rare:61 | ||||
| chr1:232950488-232950658 | Common:3; Rare:58 | ||||
| chr1:234373424-234373554 | Common:1; Rare:73; Clinvar (benign):3 | ||||
| chr1:234373666-234373766 | Rare:40; Clinvar (benign):2 | ||||
| chr1:235128674-235129025 | Rare:144 | ||||
| chr1:235328804-235329042 | Common:1; Rare:79 | ||||
| chr1:235866858-235867184 | Common:3; Rare:105 | ||||
| chr1:236065058-236065294 | Common:2; Rare:97; Clinvar (pathogenic):1 | ||||
| chr1:236281924-236282193 | Common:5; Rare:75 | ||||
| chr1:236523602-236523734 | Common:1; Rare:29 | ||||
| chr1:236523835-236524060 | Common:3; Rare:58 | ||||
| chr1:236604436-236604645 | Common:4; Rare:67 | ||||
| chr1:236795000-236795453 | Common:6; Rare:177; Clinvar:3 | ||||
| chr1:239386540-239386672 | Rare:17 | ||||
| chr1:241519674-241519963 | Common:2; Rare:94; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 |