| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48473010-48473249 | Common:1; Rare:54 | ||||
| chr3:48847663-48847962 | Common:1; Rare:81 | ||||
| chr3:48918758-48918895 | Common:2; Rare:81 | ||||
| chr3:49007181-49007432 | Common:2; Rare:98 | ||||
| chr3:49018552-49018630 | Rare:28 | ||||
| chr3:49021502-49021720 | Rare:55; Clinvar:1 | ||||
| chr3:49028299-49028527 | Rare:67 | ||||
| chr3:49029353-49029564 | Common:2; Rare:153 | ||||
| chr3:49104615-49104880 | Common:1; Rare:108; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49132912-49133093 | Rare:32; Clinvar:1 | ||||
| chr3:49339994-49340127 | Common:2; Rare:63 | ||||
| chr3:49358025-49358509 | Common:4; Rare:245 | ||||
| chr3:49411557-49411734 | Common:1; Rare:52 | ||||
| chr3:49411839-49412427 | Common:2; Rare:210 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 |