| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108730403-108730458 | Rare:17 | ||||
| chr12:109093626-109093903 | Common:2; Rare:62 | ||||
| chr12:109097512-109097654 | Rare:57; Clinvar:2 | ||||
| chr12:109097847-109098223 | Common:5; Rare:119 | ||||
| chr12:109477287-109477667 | Common:3; Rare:96 | ||||
| chr12:109573421-109573840 | Common:5; Rare:140; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880689 | Common:1; Rare:95 | ||||
| chr12:109900198-109900360 | Rare:63 | ||||
| chr12:109996215-109996439 | Common:2; Rare:65 | ||||
| chr12:109999096-109999223 | Rare:21 | ||||
| chr12:110450253-110450444 | Common:2; Rare:72 | ||||
| chr12:110468185-110468503 | Common:3; Rare:104 | ||||
| chr12:110468659-110468944 | Rare:81 | ||||
| chr12:110502058-110502241 | Common:1; Rare:64 | ||||
| chr12:110742658-110742678 | Common:1; Rare:3 |