| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141332602-141332786 | Rare:46 | ||||
| chr4:143350219-143350410 | Common:2; Rare:35 | ||||
| chr4:150579887-150580061 | Common:1; Rare:38 | ||||
| chr4:153684143-153684314 | Common:1; Rare:58 | ||||
| chr4:168924941-168925282 | Common:5; Rare:95; Clinvar:3; Clinvar (benign):7 | ||||
| chr4:173416187-173416408 | Common:3; Rare:37 | ||||
| chr4:173509555-173509675 | Common:1; Rare:34 | ||||
| chr4:173518134-173518251 | Rare:38 | ||||
| chr4:174005549-174005855 | Common:1; Rare:54 | ||||
| chr4:184815085-184815254 | Common:2; Rare:41 | ||||
| chr4:185645938-185646213 | Rare:35 | ||||
| chr4:185665977-185666035 | Rare:13 | ||||
| chr4:185878676-185878947 | Common:2; Rare:40 | ||||
| chr4:188455514-188455581 | Common:2; Rare:13 | ||||
| chr5:784685-784870 | Common:4; Rare:56 |