| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48609502-48609902 | Common:1; Rare:286 | ||||
| chr3:48634700-48635100 | Common:4; Rare:192 | ||||
| chr3:48635337-48635744 | Common:9; Rare:594 | ||||
| chr3:48635750-48636120 | Rare:131 | ||||
| chr3:48662580-48663157 | Rare:299 | ||||
| chr3:48685766-48686100 | Common:5; Rare:266 | ||||
| chr3:48686047-48686447 | Rare:106 | ||||
| chr3:48716951-48717750 | Common:21; Rare:573 | ||||
| chr3:48739901-48740317 | Common:9; Rare:233 | ||||
| chr3:48846830-48847560 | Rare:425 | ||||
| chr3:48847570-48848130 | Common:3; Rare:506 | ||||
| chr3:48898112-48898512 | Common:1; Rare:104 | ||||
| chr3:48898493-48899301 | Rare:579; Clinvar:38; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr3:48918313-48918545 | Rare:77 | ||||
| chr3:48918570-48919150 | Common:16; Rare:1002 |