| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101697599-101697981 | Common:5; Rare:127 | ||||
| chr12:102061934-102062241 | Common:1; Rare:84 | ||||
| chr12:102120060-102120263 | Rare:83 | ||||
| chr12:102958745-102958934 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr12:103929990-103930509 | Common:9; Rare:170 | ||||
| chr12:103957110-103957346 | Common:7; Rare:65 | ||||
| chr12:103965664-103965990 | Common:2; Rare:79 | ||||
| chr12:104064103-104064622 | Common:3; Rare:119 | ||||
| chr12:104138152-104138411 | Common:1; Rare:71 | ||||
| chr12:104288817-104288956 | Rare:66 | ||||
| chr12:104958235-104958380 | Common:3; Rare:43 | ||||
| chr12:104986184-104986355 | Common:3; Rare:58 | ||||
| chr12:105107612-105107803 | Common:1; Rare:91; Clinvar:1 | ||||
| chr12:105176948-105177158 | Common:1; Rare:62 | ||||
| chr12:105236041-105236294 | Common:2; Rare:110 |