| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98901217-98901397 | Common:2; Rare:62 | ||||
| chr3:98901567-98902351 | Common:6; Rare:235 | ||||
| chr3:99638397-99638634 | Common:1; Rare:60 | ||||
| chr3:99817562-99818038 | Rare:143 | ||||
| chr3:99876124-99876256 | Rare:33 | ||||
| chr3:100401035-100401198 | Rare:46 | ||||
| chr3:100401289-100401591 | Common:1; Rare:67 | ||||
| chr3:100492379-100492676 | Common:2; Rare:102 | ||||
| chr3:100709216-100709739 | Common:8; Rare:159; Clinvar (benign):1 | ||||
| chr3:100993394-100993613 | Common:3; Rare:40 | ||||
| chr3:101513126-101513217 | Common:6; Rare:27 | ||||
| chr3:101561773-101561986 | Common:2; Rare:74 | ||||
| chr3:101574142-101574276 | Common:1; Rare:54 | ||||
| chr3:101677096-101677178 | Rare:36 | ||||
| chr3:101686482-101686894 | Common:2; Rare:163 |