| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149812969-149813306 | Common:2; Rare:112 | ||||
| chr3:149813706-149813975 | Common:1; Rare:47 | ||||
| chr3:149969946-149970346 | Rare:147 | ||||
| chr3:149970829-149971105 | Common:1; Rare:118 | ||||
| chr3:149971161-149971318 | Common:3; Rare:66 | ||||
| chr3:149971452-149971958 | Common:1; Rare:144 | ||||
| chr3:150407926-150408421 | Common:3; Rare:143 | ||||
| chr3:150408828-150408992 | Rare:50 | ||||
| chr3:150545826-150546256 | Common:9; Rare:175 | ||||
| chr3:150546403-150546815 | Common:2; Rare:147 | ||||
| chr3:150603120-150603389 | Common:2; Rare:103 | ||||
| chr3:150703844-150704283 | Common:3; Rare:110 | ||||
| chr3:150763370-150763820 | Common:3; Rare:106 | ||||
| chr3:150972500-150972970 | Common:3; Rare:162; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr3:151085545-151085712 | Rare:60 |