| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15002116-15002505 | Common:2; Rare:158 | ||||
| chr4:15004072-15004361 | Common:2; Rare:109 | ||||
| chr4:15469806-15469912 | Common:1; Rare:19 | ||||
| chr4:15655227-15655473 | Common:2; Rare:97 | ||||
| chr4:15681526-15681884 | Common:4; Rare:126 | ||||
| chr4:15962925-15963371 | Common:7; Rare:129 | ||||
| chr4:16080679-16080761 | Common:1; Rare:18 | ||||
| chr4:16083722-16083800 | Common:1; Rare:21 | ||||
| chr4:17512064-17512173 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17577074-17577567 | Common:7; Rare:214 | ||||
| chr4:17614539-17614697 | Common:2; Rare:86 | ||||
| chr4:17810560-17811080 | Common:4; Rare:154 | ||||
| chr4:18021722-18021889 | Common:2; Rare:68 | ||||
| chr4:20700313-20700506 | Common:1; Rare:82 | ||||
| chr4:21304414-21304519 | Common:2; Rare:26 |