| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106357519-106357856 | Common:6; Rare:141; Clinvar:8; Clinvar (benign):2 | ||||
| chr12:106357869-106358200 | Common:12; Rare:350; Clinvar:1 | ||||
| chr12:106774057-106774424 | Common:9; Rare:262 | ||||
| chr12:106774477-106774778 | Common:4; Rare:201 | ||||
| chr12:106774843-106774969 | Rare:53 | ||||
| chr12:106955621-106955993 | Common:3; Rare:379 | ||||
| chr12:106956010-106956420 | Common:3; Rare:142 | ||||
| chr12:106956574-106956990 | Common:1; Rare:123 | ||||
| chr12:106986966-106987322 | Common:15; Rare:238 | ||||
| chr12:107093458-107093725 | Common:1; Rare:181 | ||||
| chr12:107093750-107094117 | Common:6; Rare:276 | ||||
| chr12:107318178-107318520 | Common:15; Rare:169 | ||||
| chr12:107320174-107320500 | Common:1; Rare:120 | ||||
| chr12:107685602-107685966 | Common:6; Rare:305 | ||||
| chr12:107686010-107686153 | Rare:42 |