| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:20410072-20410362 | Common:3; Rare:43 | ||||
| chr12:20477740-20478050 | Common:2; Rare:53 | ||||
| chr12:20527878-20528278 | Rare:98 | ||||
| chr12:20588035-20588435 | Common:1; Rare:96 | ||||
| chr12:21773178-21773578 | Common:1; Rare:101; Clinvar:5; Clinvar (benign):6 | ||||
| chr12:21832074-21832474 | Common:2; Rare:156 | ||||
| chr12:22255175-22255516 | Rare:69 | ||||
| chr12:22255619-22256019 | Common:1; Rare:90 | ||||
| chr12:22262218-22262618 | Common:4; Rare:161 | ||||
| chr12:22333139-22333539 | Common:4; Rare:117 | ||||
| chr12:22625901-22626104 | Common:1; Rare:42 | ||||
| chr12:22626660-22627514 | Common:7; Rare:194 | ||||
| chr12:22787603-22787864 | Rare:47 | ||||
| chr12:22831043-22831443 | Common:3; Rare:147 | ||||
| chr12:22979894-22980549 | Common:3; Rare:163 |