| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9769845-9770031 | Common:1; Rare:50 | ||||
| chr3:9792362-9792611 | Rare:69 | ||||
| chr3:9792625-9792673 | Common:1; Rare:12 | ||||
| chr3:9792685-9793123 | Common:3; Rare:155 | ||||
| chr3:9810202-9810394 | Common:1; Rare:73 | ||||
| chr3:9843865-9844132 | Common:4; Rare:119 | ||||
| chr3:9917023-9917202 | Common:2; Rare:31 | ||||
| chr3:9933455-9934087 | Common:3; Rare:221; Clinvar:4 | ||||
| chr3:9943027-9943147 | Rare:38 | ||||
| chr3:9952303-9952663 | Common:1; Rare:68 | ||||
| chr3:9986720-9987163 | Common:4; Rare:125 | ||||
| chr3:10011065-10011457 | Common:2; Rare:107 | ||||
| chr3:10026295-10026480 | Rare:62 | ||||
| chr3:10115491-10115807 | Common:4; Rare:103 | ||||
| chr3:10141675-10142009 | Common:1; Rare:157; Clinvar:39; Clinvar (benign):34 |