| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47914503-47914668 | Common:1; Rare:54 | ||||
| chr4:48016635-48016782 | Common:1; Rare:43 | ||||
| chr4:48341251-48341581 | Common:2; Rare:134 | ||||
| chr4:48780236-48780572 | Common:2; Rare:101 | ||||
| chr4:48830977-48831258 | Rare:82 | ||||
| chr4:48906704-48906829 | Rare:36 | ||||
| chr4:51843370-51843564 | Rare:67 | ||||
| chr4:52038240-52038381 | Rare:56; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659234-52659606 | Common:1; Rare:116 | ||||
| chr4:52862180-52862317 | Common:5; Rare:60 | ||||
| chr4:53365953-53366134 | Rare:34 | ||||
| chr4:54064579-54064820 | Common:4; Rare:81 | ||||
| chr4:54228957-54229337 | Common:1; Rare:82; Clinvar (benign):4 | ||||
| chr4:55346175-55346332 | Common:3; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546805-55547032 | Common:2; Rare:80 |