| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169660040-169660261 | Common:1; Rare:42 | ||||
| chr4:169757869-169758075 | Rare:59 | ||||
| chr4:170026305-170026599 | Common:4; Rare:113 | ||||
| chr4:173168114-173168286 | Common:3; Rare:39 | ||||
| chr4:173333498-173333870 | Common:2; Rare:94 | ||||
| chr4:173369732-173369935 | Common:1; Rare:64 | ||||
| chr4:173370184-173370305 | Rare:27 | ||||
| chr4:173370690-173370982 | Common:2; Rare:74 | ||||
| chr4:173371253-173371395 | Common:2; Rare:48 | ||||
| chr4:173530195-173530462 | Common:2; Rare:61 | ||||
| chr4:174283075-174283332 | Rare:37 | ||||
| chr4:174283553-174283977 | Common:1; Rare:82 | ||||
| chr4:174522423-174522619 | Rare:62; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:176195558-176195711 | Common:1; Rare:58 | ||||
| chr4:176319721-176320176 | Common:5; Rare:136 |