| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48269770-48269996 | Common:2; Rare:56 | ||||
| chr4:48341114-48341581 | Common:2; Rare:189 | ||||
| chr4:48341795-48341977 | Rare:57 | ||||
| chr4:48780172-48780475 | Common:3; Rare:103 | ||||
| chr4:48906690-48906825 | Rare:36 | ||||
| chr4:51843369-51843545 | Rare:59 | ||||
| chr4:52659191-52659439 | Common:1; Rare:83 | ||||
| chr4:53365983-53366107 | Rare:25 | ||||
| chr4:54229220-54229406 | Common:1; Rare:32; Clinvar (benign):2 | ||||
| chr4:54230782-54230988 | Rare:46 | ||||
| chr4:55546500-55546739 | Common:4; Rare:45 | ||||
| chr4:55546801-55546996 | Common:2; Rare:69 | ||||
| chr4:55853457-55853844 | Rare:115 | ||||
| chr4:56387409-56387553 | Rare:48 | ||||
| chr4:56435473-56435973 | Common:6; Rare:164 |