| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104958202-104958380 | Common:3; Rare:52 | ||||
| chr12:105107612-105107824 | Common:1; Rare:98; Clinvar:1 | ||||
| chr12:105236018-105236271 | Common:2; Rare:107 | ||||
| chr12:106357635-106357823 | Common:3; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357988-106358132 | Common:3; Rare:57 | ||||
| chr12:106955622-106955960 | Rare:123 | ||||
| chr12:107685709-107685934 | Rare:74 | ||||
| chr12:108515051-108515319 | Common:1; Rare:79 | ||||
| chr12:108561141-108561486 | Common:4; Rare:84 | ||||
| chr12:108562394-108562699 | Common:9; Rare:126; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109052538-109052672 | Common:2; Rare:47 | ||||
| chr12:109097961-109098302 | Common:5; Rare:104 | ||||
| chr12:109131840-109131971 | Common:2; Rare:32 | ||||
| chr12:109154557-109154691 | Common:1; Rare:35 | ||||
| chr12:109477275-109477653 | Common:3; Rare:96 |