| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169010236-169010459 | Common:1; Rare:64 | ||||
| chr4:169612570-169612644 | Common:3; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620358-169620723 | Common:2; Rare:128 | ||||
| chr4:169660089-169660275 | Rare:37 | ||||
| chr4:169757869-169758101 | Rare:66 | ||||
| chr4:171812484-171812742 | Common:2; Rare:41 | ||||
| chr4:173168714-173168851 | Common:2; Rare:54 | ||||
| chr4:173333498-173333883 | Common:2; Rare:99 | ||||
| chr4:173334257-173334775 | Rare:132 | ||||
| chr4:173369744-173369971 | Common:1; Rare:75 | ||||
| chr4:173370690-173370975 | Common:2; Rare:73 | ||||
| chr4:173530173-173530462 | Common:2; Rare:65 | ||||
| chr4:174283138-174283332 | Rare:29 | ||||
| chr4:174283601-174283689 | Rare:23 | ||||
| chr4:174283694-174284017 | Common:1; Rare:65 |