| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:147844126-147844574 | Common:7; Rare:146 | ||||
| chr2:147845186-147845412 | Common:1; Rare:64 | ||||
| chr2:148020670-148021109 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr2:148644659-148644814 | Rare:41 | ||||
| chr2:148645130-148645480 | Rare:138 | ||||
| chr2:148874992-148875278 | Common:3; Rare:59 | ||||
| chr2:149330365-149330674 | Common:2; Rare:127 | ||||
| chr2:149587279-149587496 | Common:2; Rare:49 | ||||
| chr2:149587675-149587954 | Common:1; Rare:77; Clinvar:1 | ||||
| chr2:150485215-150485365 | Rare:30 | ||||
| chr2:150486340-150486740 | Rare:151 | ||||
| chr2:150487589-150487897 | Common:1; Rare:64 | ||||
| chr2:151261711-151262111 | Common:5; Rare:140 | ||||
| chr2:151409761-151409969 | Common:4; Rare:63 | ||||
| chr2:151410197-151410901 | Common:5; Rare:256 |