| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:188947591-188947778 | Rare:61 | ||||
| chr3:190321987-190322149 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:190322157-190322577 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:190513902-190514162 | Common:2; Rare:67 | ||||
| chr3:190615137-190615321 | Common:1; Rare:29 | ||||
| chr3:190862634-190862809 | Rare:47 | ||||
| chr3:191329256-191329723 | Common:4; Rare:144 | ||||
| chr3:193593088-193593404 | Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194135851-194136235 | Common:1; Rare:95 | ||||
| chr3:194351253-194351542 | Common:2; Rare:53 | ||||
| chr3:194486994-194487191 | Common:3; Rare:81 | ||||
| chr3:196082043-196082262 | Common:2; Rare:91 | ||||
| chr3:196228608-196228875 | Rare:70 | ||||
| chr3:196232949-196233107 | Common:4; Rare:34 | ||||
| chr3:196287613-196287812 | Common:1; Rare:62 |