| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98522851-98523135 | Common:1; Rare:83 | ||||
| chr3:98532145-98532315 | Rare:58; Clinvar:1 | ||||
| chr3:98532391-98532685 | Common:2; Rare:105 | ||||
| chr3:98732304-98732369 | Rare:16 | ||||
| chr3:98732427-98732519 | Rare:15 | ||||
| chr3:98732617-98733257 | Common:2; Rare:157 | ||||
| chr3:98901647-98901872 | Rare:86 | ||||
| chr3:99817529-99817956 | Common:1; Rare:137 | ||||
| chr3:99876136-99876287 | Common:1; Rare:38 | ||||
| chr3:100260677-100261028 | Rare:93 | ||||
| chr3:100334658-100334786 | Common:1; Rare:57 | ||||
| chr3:100401068-100401198 | Rare:36 | ||||
| chr3:100401369-100401634 | Common:1; Rare:57 | ||||
| chr3:100709207-100709714 | Common:9; Rare:151; Clinvar (benign):1 | ||||
| chr3:101513089-101513358 | Common:8; Rare:68 |