| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:778591-778805 | Common:5; Rare:93 | ||||
| chr1:827520-827617 | Common:1; Rare:31 | ||||
| chr1:9182288-9182494 | Common:2; Rare:58 | ||||
| chr1:9687460-9687635 | Common:1; Rare:41 | ||||
| chr1:10361539-10361739 | Common:1; Rare:48; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:12713782-12714038 | Common:1; Rare:42 | ||||
| chr1:15834891-15835158 | Common:2; Rare:116 | ||||
| chr1:16644637-16644779 | Common:1; Rare:2 | ||||
| chr1:16914003-16914100 | Common:4; Rare:16 | ||||
| chr1:16976532-16976747 | Common:1; Rare:54 | ||||
| chr1:18298323-18298658 | Common:4; Rare:63 | ||||
| chr1:19787043-19787208 | Common:2; Rare:21 | ||||
| chr1:22025331-22025515 | Common:6; Rare:50 | ||||
| chr1:23082014-23082347 | Rare:54 | ||||
| chr1:23082445-23082484 | Rare:4 |