| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102120069-102120254 | Rare:73 | ||||
| chr12:102480487-102480565 | Rare:11 | ||||
| chr12:103930305-103930536 | Common:5; Rare:98 | ||||
| chr12:103957109-103957277 | Common:3; Rare:50 | ||||
| chr12:103965624-103965941 | Common:2; Rare:85 | ||||
| chr12:104064103-104064173 | Rare:13 | ||||
| chr12:104064435-104064555 | Rare:29 | ||||
| chr12:104138164-104138415 | Common:1; Rare:73 | ||||
| chr12:104958235-104958380 | Common:3; Rare:43 | ||||
| chr12:104986208-104986346 | Common:2; Rare:41 | ||||
| chr12:105107609-105107786 | Common:1; Rare:79 | ||||
| chr12:105236058-105236279 | Common:2; Rare:96 | ||||
| chr12:106357730-106357823 | Common:2; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:106955488-106955832 | Common:1; Rare:121 | ||||
| chr12:107685685-107685856 | Rare:57 |