| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97821939-97822084 | Rare:53 | ||||
| chr3:97972385-97972511 | Common:3; Rare:50 | ||||
| chr3:98522851-98523034 | Common:1; Rare:63 | ||||
| chr3:98732445-98732532 | Rare:15 | ||||
| chr3:98732578-98732698 | Rare:21 | ||||
| chr3:98901106-98901211 | Common:2; Rare:43 | ||||
| chr3:98901638-98902016 | Common:1; Rare:144 | ||||
| chr3:99638472-99638616 | Common:1; Rare:33 | ||||
| chr3:99817578-99817972 | Rare:123 | ||||
| chr3:100260688-100261034 | Rare:94 | ||||
| chr3:100401383-100401592 | Common:1; Rare:44 | ||||
| chr3:100492431-100492619 | Common:2; Rare:65 | ||||
| chr3:100709214-100709721 | Common:9; Rare:154; Clinvar (benign):1 | ||||
| chr3:101513126-101513365 | Common:8; Rare:60 | ||||
| chr3:101561759-101561955 | Common:2; Rare:73 |