| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185152878-185153087 | Common:4; Rare:71 | ||||
| chr3:185282855-185283027 | Common:1; Rare:42 | ||||
| chr3:185498237-185498461 | Rare:48 | ||||
| chr3:185498874-185499195 | Rare:114 | ||||
| chr3:185586017-185586358 | Common:1; Rare:75 | ||||
| chr3:186567289-186567441 | Common:3; Rare:38 | ||||
| chr3:186783248-186783610 | Common:1; Rare:147 | ||||
| chr3:188152902-188153109 | Common:1; Rare:32 | ||||
| chr3:188153761-188154250 | Common:1; Rare:117 | ||||
| chr3:191329551-191329719 | Common:2; Rare:50 | ||||
| chr3:192917809-192917963 | Common:1; Rare:71 | ||||
| chr3:193593101-193593402 | Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486988-194487146 | Common:3; Rare:72 | ||||
| chr3:194672133-194672471 | Common:1; Rare:110 | ||||
| chr3:195543123-195543483 | Common:4; Rare:122 |