| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71752803-71753732 | Common:5; Rare:330 | ||||
| chr3:71753731-71754349 | Common:8; Rare:339 | ||||
| chr3:72447111-72447322 | Rare:75 | ||||
| chr3:72847880-72848751 | Common:10; Rare:523 | ||||
| chr3:72996600-72996862 | Common:3; Rare:102 | ||||
| chr3:72997325-72998052 | Common:3; Rare:238 | ||||
| chr3:73624937-73625097 | Common:4; Rare:43 | ||||
| chr3:75785533-75785709 | Common:4; Rare:19 | ||||
| chr3:77038839-77039523 | Common:1; Rare:158 | ||||
| chr3:77039819-77039930 | Rare:38 | ||||
| chr3:77039940-77040230 | Common:3; Rare:80; Clinvar:2 | ||||
| chr3:77040521-77041387 | Common:3; Rare:322; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:79017954-79019012 | Common:3; Rare:300 | ||||
| chr3:79019430-79019880 | Common:4; Rare:105 | ||||
| chr3:84958690-84959090 | Common:7; Rare:177 |