| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184248868-184249008 | Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249459-184249777 | Common:1; Rare:93 | ||||
| chr3:184298944-184299283 | Common:3; Rare:106 | ||||
| chr3:184314428-184314672 | Common:3; Rare:73 | ||||
| chr3:184315408-184315495 | Rare:27 | ||||
| chr3:184711787-184712243 | Common:2; Rare:150 | ||||
| chr3:185282868-185283060 | Common:1; Rare:54 | ||||
| chr3:185498968-185499155 | Rare:66 | ||||
| chr3:185582127-185582651 | Common:2; Rare:100 | ||||
| chr3:185586000-185586326 | Common:1; Rare:72 | ||||
| chr3:185824805-185824919 | Rare:26 | ||||
| chr3:186783272-186783613 | Common:1; Rare:141 | ||||
| chr3:186806391-186806547 | Rare:48 | ||||
| chr3:186930333-186930760 | Common:3; Rare:107 | ||||
| chr3:187180725-187181252 | Common:7; Rare:125 |