| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:163988852-163989018 | Common:1; Rare:29 | ||||
| chr4:164383330-164383625 | Common:3; Rare:72 | ||||
| chr4:164383855-164384174 | Common:1; Rare:69 | ||||
| chr4:164956894-164957025 | Common:2; Rare:40 | ||||
| chr4:165112819-165113015 | Common:1; Rare:57 | ||||
| chr4:165327287-165327876 | Common:4; Rare:173 | ||||
| chr4:165378777-165379478 | Common:3; Rare:166 | ||||
| chr4:168831954-168832103 | Common:2; Rare:45 | ||||
| chr4:169010227-169010509 | Common:2; Rare:88 | ||||
| chr4:169270866-169271168 | Common:2; Rare:95 | ||||
| chr4:169612547-169612666 | Common:4; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:169620406-169620725 | Common:2; Rare:106 | ||||
| chr4:169660034-169660572 | Common:2; Rare:104 | ||||
| chr4:169757831-169758117 | Common:2; Rare:88 | ||||
| chr4:170089285-170089544 | Common:1; Rare:62 |