| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:693041-693209 | Rare:55 | ||||
| chr6:2245418-2245829 | Common:1; Rare:137 | ||||
| chr6:2902810-2902892 | Rare:14 | ||||
| chr6:2971251-2971681 | Common:6; Rare:108 | ||||
| chr6:2988484-2988741 | Common:2; Rare:40 | ||||
| chr6:2999621-2999990 | Common:10; Rare:79 | ||||
| chr6:3063809-3063967 | Common:1; Rare:62 | ||||
| chr6:3118581-3118750 | Common:2; Rare:57 | ||||
| chr6:3157407-3157629 | Common:6; Rare:75; Clinvar (benign):1 | ||||
| chr6:3227513-3227966 | Rare:111 | ||||
| chr6:3231729-3231881 | Rare:25 | ||||
| chr6:3258825-3259184 | Rare:129 | ||||
| chr6:3456034-3456198 | Rare:49 | ||||
| chr6:3849160-3849426 | Common:3; Rare:72 | ||||
| chr6:4021193-4021449 | Rare:110 |