| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110449816-110449964 | Common:1; Rare:29 | ||||
| chr12:110450048-110450493 | Common:3; Rare:136 | ||||
| chr12:110450808-110450891 | Common:3; Rare:16 | ||||
| chr12:110468079-110468585 | Common:3; Rare:167 | ||||
| chr12:110468675-110468941 | Rare:73 | ||||
| chr12:110469120-110469433 | Common:1; Rare:56 | ||||
| chr12:110501483-110501617 | Common:1; Rare:39 | ||||
| chr12:110501644-110501796 | Rare:57 | ||||
| chr12:110501881-110502424 | Common:1; Rare:219 | ||||
| chr12:110502527-110502624 | Common:1; Rare:22 | ||||
| chr12:110582902-110582959 | Common:2; Rare:25 | ||||
| chr12:110583180-110583522 | Rare:98 | ||||
| chr12:110613935-110614223 | Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110689101-110689347 | Common:1; Rare:54 | ||||
| chr12:110742298-110742510 | Common:2; Rare:61 |