| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45363394-45363527 | Common:1; Rare:35 | ||||
| chr20:45406541-45406697 | Rare:41 | ||||
| chr20:45791890-45791998 | Rare:45 | ||||
| chr20:45857343-45857616 | Common:3; Rare:70 | ||||
| chr20:45891252-45891360 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:45912150-45912314 | Common:3; Rare:37 | ||||
| chr20:46364354-46364535 | Rare:67 | ||||
| chr20:46406571-46406782 | Common:2; Rare:52 | ||||
| chr20:46709471-46709668 | Rare:53 | ||||
| chr20:47318731-47319004 | Common:1; Rare:87 | ||||
| chr20:47501720-47502000 | Common:1; Rare:96 | ||||
| chr20:49219281-49219455 | Rare:90 | ||||
| chr20:49278039-49278269 | Rare:64 | ||||
| chr20:50113124-50113272 | Common:6; Rare:67 | ||||
| chr20:50958497-50958834 | Common:1; Rare:107; Clinvar:1; Clinvar (benign):3 |