| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383268-39383443 | Common:2; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383508-39383692 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39406555-39406771 | Common:6; Rare:88 | ||||
| chr3:39406921-39407075 | Common:3; Rare:62 | ||||
| chr3:40309456-40309891 | Common:9; Rare:142 | ||||
| chr3:40457185-40457410 | Common:3; Rare:110 | ||||
| chr3:40505940-40506153 | Rare:45 | ||||
| chr3:40524795-40525013 | Common:1; Rare:63 | ||||
| chr3:41962032-41962308 | Common:4; Rare:66 | ||||
| chr3:42160063-42160221 | Common:1; Rare:33 | ||||
| chr3:42581877-42582143 | Common:3; Rare:82 | ||||
| chr3:42582256-42582359 | Rare:30 | ||||
| chr3:42590685-42590985 | Common:4; Rare:98 | ||||
| chr3:42600320-42600778 | Common:3; Rare:175 | ||||
| chr3:42600907-42601004 | Rare:39 |