| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42924266-42924461 | Common:1; Rare:60 | ||||
| chr1:42929699-42929929 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr1:43119963-43120174 | Common:7; Rare:70 | ||||
| chr1:68881202-68881430 | Common:1; Rare:73 | ||||
| chr1:75678114-75678380 | Common:3; Rare:79 | ||||
| chr1:81803093-81803264 | Common:3; Rare:40 | ||||
| chr1:83182542-83182749 | Common:6; Rare:67 | ||||
| chr1:90851606-90851757 | Common:2; Rare:39 | ||||
| chr1:112849807-112849877 | Common:1; Rare:12 | ||||
| chr1:114023423-114023618 | Common:2; Rare:26 | ||||
| chr1:116418544-116418728 | Common:2; Rare:61 | ||||
| chr1:120850983-120851265 | Rare:18 | ||||
| chr1:120942306-120942598 | Common:2; Rare:100 | ||||
| chr1:144412281-144412576 | Common:4; Rare:85 | ||||
| chr1:144524013-144524313 | Common:1; Rare:77 |