| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95526652-95526886 | Common:1; Rare:76 | ||||
| chr2:95641921-95642185 | Rare:24 | ||||
| chr2:96010432-96010605 | Rare:42 | ||||
| chr2:96297483-96297708 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:96321869-96322035 | Common:1; Rare:41 | ||||
| chr2:96842651-96842904 | Rare:43 | ||||
| chr2:97637243-97637434 | Common:1; Rare:23 | ||||
| chr2:100819096-100819215 | Common:1; Rare:16 | ||||
| chr2:101008130-101008454 | Common:2; Rare:107 | ||||
| chr2:101983629-101983783 | Common:1; Rare:21 | ||||
| chr2:102037761-102037923 | Common:2; Rare:30 | ||||
| chr2:107529317-107529544 | Common:1; Rare:44 | ||||
| chr2:107531602-107531822 | Common:1; Rare:43 | ||||
| chr2:108492278-108492642 | Common:1; Rare:84 | ||||
| chr2:108637468-108637604 | Rare:23 |