| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97747309-97747547 | Rare:46 | ||||
| chr3:97764491-97764569 | Rare:11 | ||||
| chr3:97764700-97764833 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821931-97822251 | Common:2; Rare:109 | ||||
| chr3:97972370-97972497 | Common:3; Rare:52 | ||||
| chr3:98522591-98522739 | Rare:34 | ||||
| chr3:98522851-98523050 | Common:1; Rare:67 | ||||
| chr3:98523057-98523174 | Rare:26 | ||||
| chr3:98732438-98732508 | Rare:14 | ||||
| chr3:98732677-98732711 | Rare:11 | ||||
| chr3:98901128-98901346 | Common:4; Rare:90 | ||||
| chr3:98901581-98902012 | Common:1; Rare:161 | ||||
| chr3:99817555-99817986 | Rare:133 | ||||
| chr3:99876085-99876304 | Common:2; Rare:62 | ||||
| chr3:100260691-100260868 | Rare:44 |