| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99732076-99732335 | Rare:95; Clinvar:3 | ||||
| chr10:100185920-100186091 | Rare:68 | ||||
| chr10:100267613-100267779 | Common:2; Rare:51 | ||||
| chr10:100286335-100286717 | Common:4; Rare:137 | ||||
| chr10:100346928-100347438 | Common:3; Rare:117 | ||||
| chr10:100912751-100913031 | Common:1; Rare:86 | ||||
| chr10:100987228-100987573 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031130-101031264 | Rare:33 | ||||
| chr10:101588211-101588333 | Rare:49 | ||||
| chr10:102395558-102395735 | Common:1; Rare:49 | ||||
| chr10:102432546-102432703 | Common:1; Rare:40 | ||||
| chr10:102714194-102714643 | Common:2; Rare:149 | ||||
| chr10:103396411-103396699 | Rare:103 | ||||
| chr10:103918111-103918436 | Common:4; Rare:87 | ||||
| chr10:104268949-104269193 | Common:3; Rare:59 |