| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4648992-4649149 | Common:2; Rare:52; Clinvar (benign):1 | ||||
| chr12:6451775-6452120 | Common:4; Rare:62 | ||||
| chr12:6493234-6493380 | Common:6; Rare:41 | ||||
| chr12:6493700-6494001 | Common:2; Rare:93 | ||||
| chr12:6534616-6534859 | Common:3; Rare:98 | ||||
| chr12:6723858-6724182 | Common:1; Rare:69 | ||||
| chr12:6766590-6766745 | Rare:36 | ||||
| chr12:6851226-6851486 | Rare:63 | ||||
| chr12:6867376-6867534 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr12:6970569-6971076 | Common:9; Rare:159; Clinvar (benign):2 | ||||
| chr12:7108532-7108701 | Common:1; Rare:37 | ||||
| chr12:11171607-11171638 | Rare:8 | ||||
| chr12:12357001-12357325 | Common:6; Rare:141 | ||||
| chr12:14803430-14803674 | Common:1; Rare:60 | ||||
| chr12:15882363-15882814 | Common:1; Rare:144 |