| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752940-6753208 | Common:6; Rare:85 | ||||
| chr12:6867355-6867561 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873282-6873479 | Common:2; Rare:56 | ||||
| chr12:6951250-6951756 | Common:2; Rare:139; Clinvar:1 | ||||
| chr12:6959946-6960066 | Rare:43 | ||||
| chr12:6970262-6970986 | Common:5; Rare:237; Clinvar (benign):1 | ||||
| chr12:7108472-7108701 | Common:1; Rare:63 | ||||
| chr12:7936024-7936069 | Rare:8 | ||||
| chr12:8066313-8066569 | Rare:35 | ||||
| chr12:8540850-8541076 | Common:1; Rare:36 | ||||
| chr12:9869262-9869649 | Common:3; Rare:57 | ||||
| chr12:9971295-9971585 | Common:1; Rare:58 | ||||
| chr12:10130045-10130352 | Common:3; Rare:62 | ||||
| chr12:10167576-10167829 | Common:4; Rare:40 | ||||
| chr12:10172043-10172270 | Rare:57 |