| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98645020-98645316 | Common:2; Rare:85 | ||||
| chr12:100573554-100573714 | Rare:55 | ||||
| chr12:101407713-101408092 | Common:3; Rare:98 | ||||
| chr12:102120065-102120257 | Rare:76 | ||||
| chr12:103930098-103930509 | Common:8; Rare:144 | ||||
| chr12:103965698-103965941 | Common:2; Rare:58 | ||||
| chr12:104064449-104064555 | Rare:27 | ||||
| chr12:104138164-104138371 | Rare:51 | ||||
| chr12:105107659-105107796 | Common:1; Rare:68 | ||||
| chr12:105236072-105236331 | Common:2; Rare:123 | ||||
| chr12:106955598-106955925 | Rare:120 | ||||
| chr12:107093513-107093634 | Rare:47 | ||||
| chr12:109477293-109477641 | Common:3; Rare:81 | ||||
| chr12:109573443-109573813 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:110502060-110502239 | Common:1; Rare:60 |