| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102917110-102917416 | Common:8; Rare:183; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
| chr12:103841154-103841444 | Common:8; Rare:196 | ||||
| chr12:103930041-103930565 | Common:12; Rare:276 | ||||
| chr12:103938026-103938851 | Common:9; Rare:251 | ||||
| chr12:103957112-103957324 | Common:9; Rare:101 | ||||
| chr12:103965645-103965986 | Common:2; Rare:82 | ||||
| chr12:104064433-104064592 | Rare:68 | ||||
| chr12:104138030-104138520 | Common:1; Rare:195 | ||||
| chr12:104286645-104287138 | Common:6; Rare:159 | ||||
| chr12:104288720-104288938 | Common:2; Rare:175 | ||||
| chr12:104958208-104958482 | Common:8; Rare:137 | ||||
| chr12:104958590-104958890 | Common:1; Rare:61 | ||||
| chr12:104986001-104986443 | Common:13; Rare:216 | ||||
| chr12:105107612-105107809 | Common:2; Rare:163; Clinvar:1 | ||||
| chr12:105236025-105236338 | Common:4; Rare:265 |