| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233462538-233462735 | Common:1; Rare:72 | ||||
| chr2:233468186-233468319 | Common:4; Rare:25 | ||||
| chr2:233485903-233486083 | Common:2; Rare:46 | ||||
| chr2:233488289-233488566 | Common:3; Rare:60 | ||||
| chr2:233706203-233706430 | Common:1; Rare:36 | ||||
| chr2:236989056-236989111 | Rare:10 | ||||
| chr2:237326675-237326744 | Rare:10 | ||||
| chr2:237354897-237354963 | Common:1; Rare:22; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:237502165-237502480 | Common:8; Rare:45 | ||||
| chr2:237513366-237513534 | Rare:34 | ||||
| chr2:237515480-237515712 | Common:4; Rare:49 | ||||
| chr2:237577348-237577645 | Common:2; Rare:78 | ||||
| chr2:238250665-238250853 | Rare:44 | ||||
| chr2:239267498-239267637 | Rare:32 | ||||
| chr2:240456694-240456807 | Rare:28 |