| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383258-39383466 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383537-39383709 | Rare:40; Clinvar:2 | ||||
| chr3:39406369-39406881 | Common:7; Rare:188 | ||||
| chr3:39809337-39809624 | Common:1; Rare:93 | ||||
| chr3:40309382-40309861 | Common:9; Rare:150 | ||||
| chr3:40457164-40457424 | Common:4; Rare:121 | ||||
| chr3:40457537-40457609 | Rare:23 | ||||
| chr3:40476887-40476909 | Rare:3 | ||||
| chr3:40477038-40477317 | Common:2; Rare:65 | ||||
| chr3:40505609-40505817 | Rare:37 | ||||
| chr3:40505889-40506159 | Rare:65 | ||||
| chr3:40524734-40525192 | Common:2; Rare:115 | ||||
| chr3:41199274-41199558 | Common:1; Rare:132 | ||||
| chr3:41962053-41962417 | Common:4; Rare:88 | ||||
| chr3:41962428-41962603 | Common:3; Rare:41 |