| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190890915-190891060 | Common:1; Rare:25 | ||||
| chr2:190897572-190897861 | Common:1; Rare:41 | ||||
| chr2:190899104-190899342 | Rare:52 | ||||
| chr2:190901677-190902027 | Rare:82 | ||||
| chr2:190905061-190905535 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
| chr2:190912065-190912368 | Common:1; Rare:35 | ||||
| chr2:190912976-190913245 | Common:1; Rare:41 | ||||
| chr2:190913907-190914195 | Rare:57 | ||||
| chr2:190925095-190925224 | Common:1; Rare:24 | ||||
| chr2:190942949-190943194 | Rare:47 | ||||
| chr2:190948700-190948909 | Common:1; Rare:40 | ||||
| chr2:190950518-190950796 | Common:2; Rare:53 | ||||
| chr2:190953369-190953642 | Common:2; Rare:60 | ||||
| chr2:190954161-190954403 | Common:2; Rare:39 | ||||
| chr2:190954414-190954818 | Common:1; Rare:81 |