| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101877426-101877775 | Common:4; Rare:92 | ||||
| chr12:102120069-102120235 | Rare:64 | ||||
| chr12:102480457-102480758 | Rare:38 | ||||
| chr12:103930033-103930563 | Common:9; Rare:178 | ||||
| chr12:103943582-103943881 | Rare:57 | ||||
| chr12:103965705-103965941 | Common:2; Rare:55 | ||||
| chr12:104064451-104064669 | Rare:58 | ||||
| chr12:104128425-104128690 | Rare:48 | ||||
| chr12:104138153-104138418 | Common:1; Rare:76 | ||||
| chr12:104287204-104287368 | Rare:42 | ||||
| chr12:104958254-104958454 | Common:3; Rare:60 | ||||
| chr12:105107621-105107797 | Common:1; Rare:83 | ||||
| chr12:105236078-105236269 | Common:2; Rare:89 | ||||
| chr12:106357660-106357812 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:107685685-107685929 | Rare:78 |