| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:114405697-114405865 | Common:1; Rare:30 | ||||
| chr12:114405984-114406277 | Common:1; Rare:61 | ||||
| chr12:114408000-114408198 | Common:1; Rare:36; Clinvar (benign):2 | ||||
| chr12:118103846-118104128 | Common:1; Rare:70 | ||||
| chr12:118135977-118136237 | Common:2; Rare:73 | ||||
| chr12:119179120-119179171 | Rare:9 | ||||
| chr12:120116747-120116924 | Common:2; Rare:55 | ||||
| chr12:120194693-120194804 | Rare:42 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120250007-120250217 | Common:2; Rare:30 | ||||
| chr12:120446353-120446470 | Common:1; Rare:53 | ||||
| chr12:120469509-120469895 | Common:4; Rare:134 | ||||
| chr12:120495900-120496226 | Common:6; Rare:104 | ||||
| chr12:120581348-120581586 | Common:1; Rare:81 | ||||
| chr12:120649817-120650075 | Common:8; Rare:55 |