| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177441886-177442316 | Common:10; Rare:504; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr4:177442340-177442730 | Common:1; Rare:720; Clinvar:12; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr4:182916534-182917147 | Common:13; Rare:367 | ||||
| chr4:182917176-182917679 | Common:22; Rare:639 | ||||
| chr4:182917900-182918390 | Common:3; Rare:142 | ||||
| chr4:183098302-183098924 | Common:3; Rare:166 | ||||
| chr4:183098939-183099532 | Common:27; Rare:995 | ||||
| chr4:183443995-183444104 | Rare:23 | ||||
| chr4:183444259-183444783 | Common:10; Rare:812 | ||||
| chr4:183444843-183445384 | Common:9; Rare:305 | ||||
| chr4:183504067-183505102 | Common:31; Rare:1360 | ||||
| chr4:183505257-183505880 | Common:4; Rare:286 | ||||
| chr4:183505890-183506152 | Common:1; Rare:260 | ||||
| chr4:183506252-183506510 | Common:11; Rare:277 | ||||
| chr4:183659018-183659761 | Common:8; Rare:686 |