| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013862-43014287 | Common:2; Rare:96 | ||||
| chr6:43171101-43171316 | Rare:67 | ||||
| chr6:43427783-43427902 | Rare:29 | ||||
| chr6:43477486-43477600 | Rare:25 | ||||
| chr6:43516861-43517112 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575983-43576185 | Rare:70; Clinvar:4 | ||||
| chr6:43625460-43625768 | Rare:69 | ||||
| chr6:43635740-43635876 | Common:1; Rare:35 | ||||
| chr6:44127369-44127629 | Common:4; Rare:73 | ||||
| chr6:44246904-44247199 | Common:4; Rare:124 | ||||
| chr6:45377810-45378183 | Common:2; Rare:122 | ||||
| chr6:47477589-47477789 | Rare:63 | ||||
| chr6:49463178-49463430 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420143-52420342 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671039-52671174 | Rare:43 |