| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383272-39383422 | Rare:28; Clinvar:1 | ||||
| chr3:40309522-40309819 | Common:7; Rare:103 | ||||
| chr3:40457204-40457370 | Common:2; Rare:79 | ||||
| chr3:40524821-40524960 | Common:1; Rare:32 | ||||
| chr3:42581909-42582137 | Common:3; Rare:70 | ||||
| chr3:42600533-42600709 | Common:1; Rare:70 | ||||
| chr3:42600794-42600952 | Rare:47 | ||||
| chr3:42804434-42804635 | Common:2; Rare:59 | ||||
| chr3:43690817-43690939 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477646-44477780 | Common:1; Rare:27 | ||||
| chr3:44624851-44625087 | Common:2; Rare:69 | ||||
| chr3:44761590-44761804 | Common:3; Rare:77 | ||||
| chr3:44861757-44861919 | Common:2; Rare:73 | ||||
| chr3:44976126-44976278 | Common:2; Rare:65 | ||||
| chr3:45689180-45689468 | Common:1; Rare:97 |