| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:753874-754311 | Common:2; Rare:148; Clinvar:7; Clinvar (benign):5 | ||||
| chr12:2797446-2797769 | Common:1; Rare:77 | ||||
| chr12:2800236-2800561 | Common:1; Rare:69 | ||||
| chr12:3278934-3279060 | Rare:32 | ||||
| chr12:3752430-3752564 | Common:1; Rare:26 | ||||
| chr12:6031519-6031835 | Common:3; Rare:78; Clinvar:1 | ||||
| chr12:6142829-6142991 | Common:2; Rare:53 | ||||
| chr12:6182257-6182585 | Common:4; Rare:62 | ||||
| chr12:6326257-6326555 | Common:5; Rare:75 | ||||
| chr12:6335614-6335849 | Common:1; Rare:45 | ||||
| chr12:6340697-6340985 | Rare:55 | ||||
| chr12:6450332-6450591 | Rare:66; Clinvar (benign):1 | ||||
| chr12:6450626-6451013 | Rare:103; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6927584-6927675 | Rare:32 | ||||
| chr12:6934029-6934278 | Rare:67 |