| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459831-94460028 | Common:2; Rare:56 | ||||
| chr12:95003665-95003833 | Common:3; Rare:63; Clinvar (benign):3 | ||||
| chr12:95473913-95474319 | Common:3; Rare:155 | ||||
| chr12:95996295-95996460 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96194158-96194496 | Common:6; Rare:113 | ||||
| chr12:96907168-96907262 | Common:1; Rare:28 | ||||
| chr12:98515432-98515659 | Rare:79; Clinvar:1 | ||||
| chr12:101407731-101408061 | Common:2; Rare:83 | ||||
| chr12:101877403-101877559 | Common:1; Rare:37 | ||||
| chr12:102120055-102120256 | Rare:79 | ||||
| chr12:103965705-103965910 | Common:2; Rare:53 | ||||
| chr12:103966134-103966208 | Common:3; Rare:23 | ||||
| chr12:104138170-104138362 | Rare:44 | ||||
| chr12:104456813-104457027 | Rare:80 | ||||
| chr12:105107612-105107815 | Common:1; Rare:94; Clinvar:1 |