| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100573601-100573763 | Rare:50 | ||||
| chr12:101407646-101408035 | Common:3; Rare:97 | ||||
| chr12:102120065-102120251 | Rare:71 | ||||
| chr12:103587066-103587285 | Common:1; Rare:56 | ||||
| chr12:103930282-103930557 | Common:7; Rare:112 | ||||
| chr12:103957160-103957332 | Common:5; Rare:51 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064451-104064555 | Rare:27 | ||||
| chr12:104138164-104138422 | Common:1; Rare:76 | ||||
| chr12:104958254-104958477 | Common:4; Rare:62 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236090-105236298 | Common:1; Rare:95 | ||||
| chr12:106956582-106956781 | Common:1; Rare:28 | ||||
| chr12:107685709-107685895 | Rare:66 | ||||
| chr12:108562438-108562706 | Common:9; Rare:115; Clinvar:2; Clinvar (benign):6 |