| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107612-105107806 | Common:1; Rare:92; Clinvar:1 | ||||
| chr12:105236068-105236307 | Common:2; Rare:109 | ||||
| chr12:106247370-106247525 | Common:2; Rare:36 | ||||
| chr12:106357570-106357823 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357945-106358139 | Common:3; Rare:90 | ||||
| chr12:107093510-107093619 | Rare:43 | ||||
| chr12:107318068-107318492 | Common:7; Rare:94 | ||||
| chr12:107320233-107320438 | Rare:40 | ||||
| chr12:107685709-107685971 | Rare:86 | ||||
| chr12:108515054-108515313 | Common:1; Rare:78 | ||||
| chr12:108561120-108561488 | Common:4; Rare:97 | ||||
| chr12:108562396-108562670 | Common:8; Rare:117; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:108730192-108730430 | Common:1; Rare:48 | ||||
| chr12:108731456-108731686 | Common:2; Rare:85 | ||||
| chr12:109093368-109093524 | Rare:59 |