| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51842833-51843216 | Common:1; Rare:113 | ||||
| chr4:52038240-52038431 | Rare:72; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659172-52659420 | Common:1; Rare:86 | ||||
| chr4:52862152-52862322 | Common:7; Rare:76 | ||||
| chr4:52862546-52862615 | Rare:23 | ||||
| chr4:53366037-53366134 | Rare:18 | ||||
| chr4:53377434-53377718 | Common:3; Rare:86 | ||||
| chr4:53591484-53591686 | Rare:40 | ||||
| chr4:54064567-54064880 | Common:4; Rare:103 | ||||
| chr4:55125549-55125734 | Common:3; Rare:47 | ||||
| chr4:55346169-55346332 | Common:3; Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546807-55546998 | Common:2; Rare:66 | ||||
| chr4:56387423-56387571 | Rare:53 | ||||
| chr4:56435371-56435406 | Rare:11 | ||||
| chr4:56435458-56435973 | Common:6; Rare:169 |