| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501714-47502015 | Common:1; Rare:107 | ||||
| chr20:49046171-49046354 | Common:3; Rare:54 | ||||
| chr20:49188304-49188591 | Common:2; Rare:95 | ||||
| chr20:49812712-49812925 | Common:2; Rare:56 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50115932-50116092 | Common:2; Rare:36 | ||||
| chr20:50510248-50510427 | Common:3; Rare:72 | ||||
| chr20:50958510-50958853 | Common:1; Rare:111; Clinvar (benign):2 | ||||
| chr20:51801552-51801739 | Common:2; Rare:43 | ||||
| chr20:51802278-51802781 | Common:2; Rare:133; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:53593783-53593937 | Common:1; Rare:59 | ||||
| chr20:56392153-56392465 | Common:1; Rare:96 | ||||
| chr20:56392564-56392692 | Common:1; Rare:32 | ||||
| chr20:56468374-56468700 | Rare:115 | ||||
| chr20:58388989-58389277 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):1 |