| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11720695-11720772 | Rare:8 | ||||
| chr3:12158844-12158970 | Rare:42 | ||||
| chr3:12545475-12545557 | Common:1; Rare:22 | ||||
| chr3:12585221-12585536 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:12663979-12664311 | Common:2; Rare:91; Clinvar:2; Clinvar (benign):7 | ||||
| chr3:12759192-12759444 | Common:1; Rare:60 | ||||
| chr3:12759536-12759643 | Common:2; Rare:15 | ||||
| chr3:13479993-13480334 | Common:3; Rare:88 | ||||
| chr3:14124690-14125179 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14125182-14125196 | Rare:7; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178468-14178870 | Common:3; Rare:194; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402282-14402765 | Common:5; Rare:115 | ||||
| chr3:14651423-14651818 | Common:1; Rare:116 | ||||
| chr3:14947203-14947569 | Common:4; Rare:162 | ||||
| chr3:14948019-14948131 | Rare:57 |