| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671830-158672435 | Common:5; Rare:160; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723211-158723463 | Common:2; Rare:108 | ||||
| chr4:159103805-159104165 | Common:4; Rare:128 | ||||
| chr4:163166856-163166946 | Common:2; Rare:26 | ||||
| chr4:165112786-165113015 | Common:1; Rare:75 | ||||
| chr4:165327346-165327911 | Common:4; Rare:166 | ||||
| chr4:168318681-168318823 | Rare:32 | ||||
| chr4:168318831-168318856 | Rare:4 | ||||
| chr4:168480363-168480546 | Common:1; Rare:35 | ||||
| chr4:168893757-168893993 | Common:1; Rare:50 | ||||
| chr4:169010227-169010468 | Common:1; Rare:75 | ||||
| chr4:169620360-169620725 | Common:2; Rare:128 | ||||
| chr4:169620842-169621003 | Rare:39 | ||||
| chr4:170026282-170026619 | Common:4; Rare:130 | ||||
| chr4:173167967-173168272 | Common:3; Rare:56 |