| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493785-6494126 | Common:2; Rare:103 | ||||
| chr12:6534256-6534569 | Common:6; Rare:127 | ||||
| chr12:6568253-6568382 | Rare:48 | ||||
| chr12:6688843-6689239 | Rare:118 | ||||
| chr12:6689266-6689748 | Common:3; Rare:135 | ||||
| chr12:6723830-6724286 | Common:1; Rare:101 | ||||
| chr12:6752932-6753189 | Common:6; Rare:78 | ||||
| chr12:6851902-6852191 | Rare:76 | ||||
| chr12:6873334-6873526 | Common:1; Rare:53 | ||||
| chr12:6970510-6970996 | Common:4; Rare:154; Clinvar (benign):1 | ||||
| chr12:7018420-7018563 | Common:1; Rare:47 | ||||
| chr12:7108497-7108600 | Common:1; Rare:30 | ||||
| chr12:7109149-7109398 | Rare:74 | ||||
| chr12:7128885-7128990 | Rare:17 | ||||
| chr12:7130256-7130415 | Common:4; Rare:42 |