| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108850956-108851182 | Common:5; Rare:34 | ||||
| chr12:108851210-108851288 | Common:2; Rare:17 | ||||
| chr12:108851352-108851617 | Common:1; Rare:42 | ||||
| chr12:108851719-108851837 | Rare:23 | ||||
| chr12:108851916-108851957 | Rare:10 | ||||
| chr12:108851978-108852196 | Common:1; Rare:47 | ||||
| chr12:108852638-108853034 | Common:1; Rare:97 | ||||
| chr12:108854531-108854703 | Rare:45 | ||||
| chr12:108943554-108943821 | Common:3; Rare:38 | ||||
| chr12:109102539-109102926 | Common:3; Rare:86; Clinvar:1 | ||||
| chr12:109452568-109452824 | Common:1; Rare:54 | ||||
| chr12:109453037-109453226 | Common:1; Rare:25 | ||||
| chr12:109455069-109455420 | Common:3; Rare:64 | ||||
| chr12:109463222-109463476 | Common:3; Rare:38 | ||||
| chr12:109903868-109904006 | Rare:49 |