| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38165489-38165813 | Common:1; Rare:112 | ||||
| chr3:39051924-39052050 | Common:1; Rare:44 | ||||
| chr3:39107562-39107653 | Common:1; Rare:35 | ||||
| chr3:39383288-39383432 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383582-39383676 | Rare:20; Clinvar:1 | ||||
| chr3:39406531-39406787 | Common:6; Rare:106 | ||||
| chr3:40309465-40309919 | Common:9; Rare:152 | ||||
| chr3:40457201-40457470 | Common:6; Rare:123 | ||||
| chr3:40477059-40477184 | Common:1; Rare:32 | ||||
| chr3:40505932-40506120 | Rare:43 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41962045-41962240 | Common:2; Rare:45 | ||||
| chr3:41962298-41962562 | Common:3; Rare:66 | ||||
| chr3:42581898-42582132 | Common:3; Rare:72 | ||||
| chr3:42590645-42590958 | Common:3; Rare:95 |