| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107612-105107837 | Common:1; Rare:100; Clinvar:1 | ||||
| chr12:105330829-105330933 | Rare:20 | ||||
| chr12:106247370-106247568 | Common:2; Rare:53 | ||||
| chr12:106955725-106955966 | Rare:82 | ||||
| chr12:107685705-107685950 | Rare:82 | ||||
| chr12:108561137-108561488 | Common:4; Rare:87 | ||||
| chr12:109458141-109458263 | Common:4; Rare:20 | ||||
| chr12:109458973-109459096 | Rare:20 | ||||
| chr12:109477275-109477688 | Common:3; Rare:110 | ||||
| chr12:109573483-109573819 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:109880396-109880668 | Common:1; Rare:82 | ||||
| chr12:109999066-109999259 | Rare:36 | ||||
| chr12:110280902-110281338 | Common:1; Rare:159; Clinvar (benign):1 | ||||
| chr12:110455588-110455878 | Common:1; Rare:74 | ||||
| chr12:110468711-110468915 | Rare:55 |