| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112647049-112647466 | Common:4; Rare:211 | ||||
| chr2:112720770-112721100 | Common:9; Rare:148 | ||||
| chr2:112763896-112764331 | Common:8; Rare:311 | ||||
| chr2:112764530-112765090 | Common:22; Rare:710; Clinvar (pathogenic):6 | ||||
| chr2:112765146-112765546 | Common:2; Rare:81 | ||||
| chr2:112784314-112784801 | Common:2; Rare:263 | ||||
| chr2:113157097-113157198 | Rare:27 | ||||
| chr2:113157130-113157646 | Common:14; Rare:358 | ||||
| chr2:113173750-113174050 | Common:9; Rare:189 | ||||
| chr2:113174445-113174845 | Common:1; Rare:63 | ||||
| chr2:113219939-113220339 | Common:2; Rare:175; Clinvar:9 | ||||
| chr2:113235060-113235992 | Common:14; Rare:1137; Clinvar:14; Clinvar (benign):7 | ||||
| chr2:113240934-113241334 | Rare:72 | ||||
| chr2:113241647-113242131 | Common:2; Rare:242; Clinvar:1 | ||||
| chr2:113437560-113437880 | Common:4; Rare:201 |