| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149330333-149330670 | Common:2; Rare:138 | ||||
| chr2:149330703-149330784 | Rare:17 | ||||
| chr2:149587169-149587546 | Common:3; Rare:80 | ||||
| chr2:149587659-149587970 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150485225-150485535 | Common:1; Rare:60 | ||||
| chr2:150486079-150486417 | Common:1; Rare:80 | ||||
| chr2:150486977-150487029 | Rare:4 | ||||
| chr2:150487553-150487743 | Rare:31 | ||||
| chr2:151261400-151261526 | Common:3; Rare:46 | ||||
| chr2:151261645-151261949 | Common:3; Rare:72 | ||||
| chr2:151289359-151289490 | Common:1; Rare:30 | ||||
| chr2:151289546-151289773 | Common:1; Rare:54 | ||||
| chr2:151409668-151410027 | Common:4; Rare:102 | ||||
| chr2:151410083-151410453 | Common:1; Rare:121 | ||||
| chr2:151410494-151410765 | Common:2; Rare:74 |