| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98522844-98523243 | Common:1; Rare:111 | ||||
| chr3:98593553-98593901 | Common:4; Rare:119; Clinvar (benign):3 | ||||
| chr3:98733784-98734184 | Common:11; Rare:97 | ||||
| chr3:98901010-98901410 | Common:5; Rare:192 | ||||
| chr3:98901660-98902054 | Common:1; Rare:146 | ||||
| chr3:99638310-99638840 | Common:1; Rare:114 | ||||
| chr3:99817552-99817985 | Rare:134 | ||||
| chr3:99876137-99876281 | Common:1; Rare:34 | ||||
| chr3:100260691-100261033 | Rare:91 | ||||
| chr3:100334622-100334786 | Common:1; Rare:69 | ||||
| chr3:100401034-100401237 | Rare:64 | ||||
| chr3:100401386-100401642 | Common:2; Rare:52 | ||||
| chr3:100492106-100492206 | Rare:30 | ||||
| chr3:100492390-100492648 | Common:2; Rare:90 | ||||
| chr3:100709183-100709377 | Common:4; Rare:65 |