| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12759208-12759400 | Common:1; Rare:45 | ||||
| chr3:13479993-13480334 | Common:3; Rare:88 | ||||
| chr3:13548974-13549177 | Common:1; Rare:64 | ||||
| chr3:14124728-14125186 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178870 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402306-14402632 | Common:1; Rare:88 | ||||
| chr3:14525980-14526153 | Common:2; Rare:29 | ||||
| chr3:14651468-14651830 | Rare:111 | ||||
| chr3:14947236-14947563 | Common:4; Rare:149 | ||||
| chr3:14948105-14948197 | Rare:39 | ||||
| chr3:15065213-15065359 | Common:2; Rare:61 | ||||
| chr3:15205935-15206278 | Rare:119 | ||||
| chr3:15427471-15427652 | Common:1; Rare:67 | ||||
| chr3:15601512-15601810 | Common:4; Rare:127; Clinvar:2 | ||||
| chr3:15797793-15797870 | Common:1; Rare:10 |