| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10026347-10026482 | Rare:38 | ||||
| chr3:10115512-10115702 | Common:4; Rare:69 | ||||
| chr3:10141675-10141839 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):16 | ||||
| chr3:11225904-11225976 | Rare:11 | ||||
| chr3:11272227-11272413 | Common:1; Rare:38 | ||||
| chr3:11643875-11644075 | Common:2; Rare:62 | ||||
| chr3:12484336-12484511 | Common:4; Rare:53; Clinvar (benign):1 | ||||
| chr3:12664084-12664309 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13420208-13420466 | Common:1; Rare:78 | ||||
| chr3:14124736-14125068 | Common:4; Rare:95; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178872 | Common:2; Rare:153; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402447-14402636 | Rare:49 | ||||
| chr3:14651468-14651808 | Rare:100 | ||||
| chr3:14947421-14947602 | Common:2; Rare:84 | ||||
| chr3:15065233-15065389 | Common:2; Rare:54 |