| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93677277-93677381 | Rare:22 | ||||
| chr12:94459811-94460003 | Common:3; Rare:50 | ||||
| chr12:98515353-98515774 | Common:1; Rare:143; Clinvar:2 | ||||
| chr12:101407731-101408005 | Common:2; Rare:67 | ||||
| chr12:102120065-102120257 | Rare:76 | ||||
| chr12:103930089-103930438 | Common:6; Rare:107 | ||||
| chr12:103965706-103965990 | Common:2; Rare:61 | ||||
| chr12:104138170-104138394 | Common:1; Rare:58 | ||||
| chr12:104958245-104958425 | Common:3; Rare:53 | ||||
| chr12:105107571-105107785 | Common:1; Rare:97 | ||||
| chr12:107685685-107685895 | Rare:71 | ||||
| chr12:109573466-109573845 | Common:3; Rare:114; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:110468211-110468491 | Common:3; Rare:88 | ||||
| chr12:110502037-110502244 | Common:1; Rare:72 | ||||
| chr12:112013137-112013490 | Common:1; Rare:129 |