| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3179653-3179906 | Common:3; Rare:93; Clinvar:3 | ||||
| chr3:3799819-3799853 | Rare:11 | ||||
| chr3:4303540-4303648 | Common:1; Rare:37 | ||||
| chr3:4467243-4467326 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9249624-9249750 | Common:1; Rare:35 | ||||
| chr3:9362988-9363105 | Rare:45 | ||||
| chr3:9397426-9397873 | Common:1; Rare:146 | ||||
| chr3:9749779-9749983 | Rare:68 | ||||
| chr3:9769886-9770031 | Common:1; Rare:40 | ||||
| chr3:9792376-9792524 | Rare:44 | ||||
| chr3:9792777-9793136 | Common:3; Rare:125 | ||||
| chr3:9933697-9933847 | Common:1; Rare:58 | ||||
| chr3:10026334-10026482 | Rare:42 | ||||
| chr3:10115520-10115722 | Common:3; Rare:74 | ||||
| chr3:10141678-10141855 | Common:1; Rare:81; Clinvar:11; Clinvar (benign):17 |