| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16146200-16146610 | Common:9; Rare:149 | ||||
| chr1:16155958-16156144 | Rare:80; Clinvar:4 | ||||
| chr1:16206450-16207290 | Common:15; Rare:384 | ||||
| chr1:16352415-16352580 | Common:4; Rare:174 | ||||
| chr1:16366967-16367269 | Common:2; Rare:163 | ||||
| chr1:16440522-16440785 | Common:3; Rare:145 | ||||
| chr1:16613433-16613663 | Common:3 | ||||
| chr1:17011871-17012057 | Common:1; Rare:53; Clinvar:2 | ||||
| chr1:17053961-17054375 | Common:4; Rare:200; Clinvar:17; Clinvar (benign):12 | ||||
| chr1:17439629-17439887 | Rare:162 | ||||
| chr1:17580003-17580191 | Common:2; Rare:43 | ||||
| chr1:17580323-17580586 | Common:2; Rare:86 | ||||
| chr1:18902729-18903051 | Common:11; Rare:135 | ||||
| chr1:18956607-18956967 | Common:6; Rare:188 | ||||
| chr1:19210132-19210559 | Common:2; Rare:273 |