| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573478-109573813 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109880323-109880673 | Common:1; Rare:111 | ||||
| chr12:109996212-109996457 | Common:2; Rare:70 | ||||
| chr12:110468721-110468909 | Rare:52 | ||||
| chr12:110502058-110502156 | Common:1; Rare:43 | ||||
| chr12:111685776-111686110 | Rare:127 | ||||
| chr12:111841867-111842028 | Common:2; Rare:49 | ||||
| chr12:112013129-112013472 | Common:1; Rare:120 | ||||
| chr12:112108755-112108902 | Common:1; Rare:38 | ||||
| chr12:112906831-112907000 | Rare:30 | ||||
| chr12:112938458-112938541 | Common:2; Rare:19 | ||||
| chr12:112978389-112978610 | Rare:38 | ||||
| chr12:113185388-113185769 | Common:10; Rare:149 | ||||
| chr12:113966306-113966462 | Common:3; Rare:49 | ||||
| chr12:118103889-118104099 | Common:1; Rare:50 |