| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48600460-48600500 | Rare:15 | ||||
| chr3:48634829-48634984 | Common:1; Rare:39 | ||||
| chr3:48847396-48847534 | Rare:49 | ||||
| chr3:48847660-48847989 | Common:1; Rare:92 | ||||
| chr3:48918810-48918992 | Common:2; Rare:100 | ||||
| chr3:48926807-48926940 | Common:2; Rare:25 | ||||
| chr3:48989731-48989946 | Rare:52 | ||||
| chr3:49007078-49007483 | Common:2; Rare:153 | ||||
| chr3:49007487-49007634 | Rare:37 | ||||
| chr3:49007838-49008100 | Common:2; Rare:71 | ||||
| chr3:49021503-49021791 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49022011-49022174 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49028175-49028499 | Rare:93 | ||||
| chr3:49044479-49044770 | Rare:54 | ||||
| chr3:49092887-49093153 | Common:1; Rare:66 |