| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:17742596-17742767 | Common:3; Rare:53 | ||||
| chr3:19946966-19947393 | Common:5; Rare:159 | ||||
| chr3:20186173-20186415 | Common:2; Rare:77 | ||||
| chr3:21751140-21751413 | Common:3; Rare:86 | ||||
| chr3:23916911-23917214 | Rare:115 | ||||
| chr3:24494740-24494903 | Rare:44 | ||||
| chr3:25428107-25428277 | Rare:33 | ||||
| chr3:25783388-25783641 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr3:25789932-25790118 | Common:4; Rare:71 | ||||
| chr3:27722705-27722947 | Common:3; Rare:35 | ||||
| chr3:28349041-28349179 | Common:2; Rare:43 | ||||
| chr3:29280909-29281081 | Common:2; Rare:33 | ||||
| chr3:31532291-31532608 | Common:3; Rare:99 | ||||
| chr3:32106418-32106697 | Common:4; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502795-32502889 | Rare:25 |