| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:610366-610444 | Rare:9 | ||||
| chr12:1690862-1691064 | Common:2; Rare:71 | ||||
| chr12:1811699-1811856 | Common:1; Rare:43; Clinvar:1 | ||||
| chr12:3753064-3753259 | Common:1; Rare:47 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4648998-4649141 | Common:2; Rare:44; Clinvar (benign):1 | ||||
| chr12:6451809-6452170 | Common:4; Rare:68 | ||||
| chr12:6470672-6470891 | Rare:53 | ||||
| chr12:6493245-6493394 | Common:5; Rare:40 | ||||
| chr12:6534329-6534594 | Common:5; Rare:112 | ||||
| chr12:6550415-6550784 | Common:2; Rare:81 | ||||
| chr12:6568251-6568393 | Rare:55 | ||||
| chr12:6678453-6678698 | Common:1; Rare:68 | ||||
| chr12:6723858-6724177 | Common:1; Rare:68 | ||||
| chr12:6724223-6724291 | Rare:13 |