| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169010223-169010339 | Common:1; Rare:43 | ||||
| chr4:169156677-169156685 | Rare:5 | ||||
| chr4:169270866-169271162 | Common:2; Rare:95 | ||||
| chr4:169612547-169612827 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:169620260-169620707 | Common:2; Rare:152 | ||||
| chr4:169660035-169660272 | Common:1; Rare:43 | ||||
| chr4:173168190-173168345 | Common:1; Rare:37 | ||||
| chr4:173168708-173168851 | Common:2; Rare:57 | ||||
| chr4:173370690-173370999 | Common:2; Rare:79 | ||||
| chr4:174283618-174284046 | Common:1; Rare:93 | ||||
| chr4:176319720-176320210 | Common:5; Rare:144 | ||||
| chr4:177442372-177442508 | Rare:83; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143789-182144098 | Common:3; Rare:70 | ||||
| chr4:182144111-182144219 | Common:3; Rare:32 | ||||
| chr4:182144399-182144743 | Common:4; Rare:116 |