| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48898890-48899053 | Rare:52; Clinvar:3 | ||||
| chr3:48918667-48918874 | Common:2; Rare:100 | ||||
| chr3:48989732-48989892 | Rare:41 | ||||
| chr3:48990038-48990248 | Rare:48 | ||||
| chr3:48990908-48991014 | Rare:23 | ||||
| chr3:49007129-49007455 | Common:2; Rare:134 | ||||
| chr3:49007797-49008734 | Common:5; Rare:275 | ||||
| chr3:49020211-49020522 | Common:1; Rare:67 | ||||
| chr3:49020690-49020812 | Common:1; Rare:37 | ||||
| chr3:49021475-49021764 | Common:1; Rare:69; Clinvar:1 | ||||
| chr3:49021993-49022183 | Rare:66; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029392-49029578 | Common:2; Rare:130 | ||||
| chr3:49093088-49093743 | Common:1; Rare:225 | ||||
| chr3:49093988-49094293 | Rare:73 | ||||
| chr3:49094323-49094437 | Rare:30 |