| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1890861-1891207 | Rare:131 | ||||
| chr1:2391529-2391892 | Common:2; Rare:134 | ||||
| chr1:3069081-3069190 | Rare:17 | ||||
| chr1:3624738-3625021 | Common:1; Rare:94 | ||||
| chr1:3796482-3796770 | Common:5; Rare:73 | ||||
| chr1:3857190-3857508 | Common:1; Rare:83 | ||||
| chr1:5992383-5992704 | Common:4; Rare:110; Clinvar:6 | ||||
| chr1:6026149-6026396 | Common:1; Rare:51 | ||||
| chr1:6206000-6206088 | Common:2; Rare:18 | ||||
| chr1:6208680-6208925 | Common:1; Rare:72 | ||||
| chr1:6602857-6603117 | Common:3; Rare:93 | ||||
| chr1:6613692-6613779 | Common:1; Rare:36 | ||||
| chr1:7771152-7771366 | Common:4; Rare:93 | ||||
| chr1:7954104-7954293 | Rare:48 | ||||
| chr1:7961457-7961758 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):3 |