| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48017216-48017491 | Common:2; Rare:55 | ||||
| chr4:48269816-48269971 | Common:1; Rare:30 | ||||
| chr4:48341098-48341558 | Common:2; Rare:183 | ||||
| chr4:48780236-48780572 | Common:2; Rare:101 | ||||
| chr4:48906690-48906869 | Rare:42 | ||||
| chr4:52659172-52659449 | Common:1; Rare:95 | ||||
| chr4:52862152-52862322 | Common:7; Rare:76 | ||||
| chr4:53365980-53366164 | Rare:40 | ||||
| chr4:53591476-53591768 | Common:2; Rare:56 | ||||
| chr4:54064554-54064912 | Common:4; Rare:115 | ||||
| chr4:54228937-54229409 | Common:1; Rare:94; Clinvar (benign):4 | ||||
| chr4:55395818-55395957 | Common:2; Rare:36; Clinvar:2 | ||||
| chr4:55398664-55398790 | Common:2; Rare:14 | ||||
| chr4:55546801-55547011 | Common:2; Rare:73 | ||||
| chr4:55948717-55948928 | Common:1; Rare:42 |