| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48635356-48635721 | Common:3; Rare:191 | ||||
| chr3:48662876-48663002 | Rare:23 | ||||
| chr3:48662904-48663017 | Rare:21 | ||||
| chr3:48716951-48717751 | Common:9; Rare:270 | ||||
| chr3:48847646-48847973 | Common:2; Rare:171 | ||||
| chr3:48898817-48899051 | Rare:132; Clinvar:12 | ||||
| chr3:48918754-48918938 | Common:4; Rare:198 | ||||
| chr3:49007148-49007572 | Common:4; Rare:289 | ||||
| chr3:49007690-49008170 | Common:5; Rare:211 | ||||
| chr3:49021491-49021746 | Rare:117; Clinvar:2 | ||||
| chr3:49029365-49029467 | Common:1; Rare:73 | ||||
| chr3:49093440-49093743 | Common:1; Rare:169 | ||||
| chr3:49093988-49094262 | Rare:102 | ||||
| chr3:49104691-49105001 | Common:1; Rare:205; Clinvar:1; Clinvar (benign):8 | ||||
| chr3:49120745-49121001 | Rare:75 |