| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88580432-88580556 | Common:2; Rare:43 | ||||
| chr12:89524756-89524869 | Common:1; Rare:21 | ||||
| chr12:92929285-92929492 | Rare:59 | ||||
| chr12:93377746-93377929 | Rare:45 | ||||
| chr12:93441866-93442147 | Common:2; Rare:90 | ||||
| chr12:93571737-93571912 | Common:7; Rare:67 | ||||
| chr12:94459833-94460018 | Common:2; Rare:53 | ||||
| chr12:95003627-95003820 | Common:3; Rare:76; Clinvar (benign):4 | ||||
| chr12:95217427-95217769 | Common:3; Rare:92 | ||||
| chr12:96400559-96400875 | Rare:99 | ||||
| chr12:96907180-96907285 | Rare:40 | ||||
| chr12:98644997-98645327 | Common:2; Rare:98 | ||||
| chr12:100573569-100573740 | Rare:60 | ||||
| chr12:101407662-101408020 | Common:3; Rare:85 | ||||
| chr12:102061948-102062179 | Common:1; Rare:66 |