| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:72997832-72998102 | Rare:87 | ||||
| chr3:75785495-75785724 | Common:4; Rare:33 | ||||
| chr3:79018070-79018176 | Rare:24 | ||||
| chr3:79018812-79018841 | Common:1; Rare:11 | ||||
| chr3:79018961-79019131 | Rare:49 | ||||
| chr3:79019343-79019575 | Common:4; Rare:72 | ||||
| chr3:81761003-81761914 | Common:10; Rare:307; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:87227096-87227377 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:87227703-87227743 | Rare:6 | ||||
| chr3:88058575-88058809 | Common:1; Rare:71 | ||||
| chr3:88058896-88059374 | Common:3; Rare:183 | ||||
| chr3:88149561-88150207 | Common:7; Rare:196 | ||||
| chr3:88150329-88150536 | Common:1; Rare:43 | ||||
| chr3:93979916-93980261 | Common:4; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:93980388-93980455 | Rare:34; Clinvar:2 |