| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:164956901-164957025 | Common:2; Rare:39 | ||||
| chr4:164977591-164977734 | Rare:37 | ||||
| chr4:165112761-165113015 | Common:1; Rare:86 | ||||
| chr4:165327400-165327835 | Common:2; Rare:126 | ||||
| chr4:165378843-165379526 | Common:3; Rare:165 | ||||
| chr4:168318676-168318890 | Rare:44 | ||||
| chr4:168480289-168480522 | Common:1; Rare:57 | ||||
| chr4:168631480-168631833 | Common:1; Rare:90 | ||||
| chr4:168893983-168893988 | |||||
| chr4:168894492-168894675 | Rare:48; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:168921354-168921741 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169010051-169010494 | Common:6; Rare:140 | ||||
| chr4:169270853-169271183 | Common:2; Rare:102 | ||||
| chr4:169612547-169612771 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:169620358-169620776 | Common:2; Rare:138 |