| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95474006-95474185 | Common:2; Rare:82 | ||||
| chr12:95548791-95548914 | Common:2; Rare:43 | ||||
| chr12:95551361-95551570 | Common:3; Rare:36 | ||||
| chr12:95858797-95859033 | Common:2; Rare:66 | ||||
| chr12:96907185-96907295 | Rare:41 | ||||
| chr12:98515402-98515675 | Common:1; Rare:92; Clinvar:1 | ||||
| chr12:98593481-98593765 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:100267060-100267267 | Common:1; Rare:99 | ||||
| chr12:101407731-101408035 | Common:2; Rare:73 | ||||
| chr12:102120058-102120257 | Rare:79 | ||||
| chr12:103965705-103965947 | Common:2; Rare:56 | ||||
| chr12:104138152-104138421 | Common:1; Rare:77 | ||||
| chr12:107093527-107093665 | Rare:47 | ||||
| chr12:107685689-107685860 | Rare:58 | ||||
| chr12:108561150-108561463 | Common:4; Rare:75 |