| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:49550450-49550689 | Rare:51 | ||||
| chr6:52284676-52285094 | Common:2; Rare:140 | ||||
| chr6:52420101-52420385 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671031-52671219 | Rare:47 | ||||
| chr6:52995609-52995813 | Rare:96 | ||||
| chr6:53065344-53065614 | Common:1; Rare:86 | ||||
| chr6:53348882-53349211 | Common:2; Rare:127 | ||||
| chr6:56542776-56542999 | Common:1; Rare:37 | ||||
| chr6:57046511-57046758 | Rare:87 | ||||
| chr6:57172502-57172758 | Common:1; Rare:80 | ||||
| chr6:57222266-57222362 | Rare:36 | ||||
| chr6:57317539-57317667 | Rare:39 | ||||
| chr6:63572259-63572596 | Rare:128 | ||||
| chr6:63636045-63636140 | Rare:32 | ||||
| chr6:69796867-69797135 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):2 |