| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663433-97663638 | Common:2; Rare:57 | ||||
| chr2:97663982-97664367 | Rare:107 | ||||
| chr2:97995031-97995537 | Common:6; Rare:142 | ||||
| chr2:97995726-97995985 | Common:3; Rare:87 | ||||
| chr2:97996191-97996497 | Common:2; Rare:96 | ||||
| chr2:98444670-98444956 | Common:1; Rare:114 | ||||
| chr2:98608414-98608689 | Common:1; Rare:114; Clinvar (benign):1 | ||||
| chr2:98609180-98609263 | Common:1; Rare:18 | ||||
| chr2:98730915-98731359 | Common:5; Rare:144 | ||||
| chr2:99140891-99141045 | Rare:30 | ||||
| chr2:99141105-99141356 | Common:1; Rare:99 | ||||
| chr2:99154803-99155168 | Common:7; Rare:139; Clinvar (benign):3 | ||||
| chr2:99155432-99155525 | Common:1; Rare:29 | ||||
| chr2:99180940-99181275 | Common:2; Rare:100 | ||||
| chr2:99336010-99336394 | Common:1; Rare:113 |