| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47837421-47837542 | Common:1; Rare:18 | ||||
| chr4:47837725-47837806 | Rare:15 | ||||
| chr4:47837921-47838212 | Common:1; Rare:61; Clinvar:1 | ||||
| chr4:48016624-48016774 | Common:1; Rare:41 | ||||
| chr4:48269807-48269989 | Common:1; Rare:37 | ||||
| chr4:48341275-48341581 | Common:1; Rare:126 | ||||
| chr4:48780197-48780605 | Common:3; Rare:125 | ||||
| chr4:52038228-52038331 | Rare:47; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr4:52659172-52659439 | Common:1; Rare:91 | ||||
| chr4:52751393-52751524 | Rare:31 | ||||
| chr4:52862180-52862322 | Common:5; Rare:63 | ||||
| chr4:53365997-53366184 | Rare:41 | ||||
| chr4:53652423-53652708 | Common:2; Rare:45 | ||||
| chr4:55346159-55346337 | Common:3; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395845-55395957 | Common:1; Rare:30; Clinvar:2 |