| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236348196-236348302 | Common:2; Rare:26 | ||||
| chr1:236523878-236524080 | Common:2; Rare:57 | ||||
| chr1:236524532-236524608 | Common:1; Rare:13 | ||||
| chr1:236541385-236541702 | Common:13; Rare:77 | ||||
| chr1:236604447-236604593 | Common:4; Rare:50 | ||||
| chr1:236795151-236795519 | Common:5; Rare:153; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:237799946-237800052 | Common:4; Rare:27 | ||||
| chr1:239386462-239386603 | Rare:22 | ||||
| chr1:239408035-239408193 | Common:3; Rare:37 | ||||
| chr1:241519628-241519977 | Common:3; Rare:112; Clinvar:14; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr1:241639557-241639892 | Common:5; Rare:86 | ||||
| chr1:241652132-241652317 | Rare:27 | ||||
| chr1:241848038-241848280 | Common:3; Rare:54 | ||||
| chr1:243163283-243163424 | Common:1; Rare:15 | ||||
| chr1:243255045-243255463 | Common:1; Rare:99 |