| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45891206-45891387 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:46364381-46364551 | Rare:64 | ||||
| chr20:46406571-46406793 | Common:2; Rare:59 | ||||
| chr20:46709589-46709681 | Rare:26; Clinvar:1 | ||||
| chr20:47318731-47318989 | Common:1; Rare:82 | ||||
| chr20:47318997-47319092 | Rare:26 | ||||
| chr20:47356664-47356863 | Rare:43 | ||||
| chr20:47501555-47501940 | Common:2; Rare:119 | ||||
| chr20:49046183-49046363 | Common:3; Rare:54 | ||||
| chr20:49219200-49219464 | Common:1; Rare:119 | ||||
| chr20:49278039-49278220 | Rare:50 | ||||
| chr20:50113118-50113254 | Common:5; Rare:65 | ||||
| chr20:50115926-50116087 | Common:2; Rare:38 | ||||
| chr20:50153651-50153881 | Common:2; Rare:93 | ||||
| chr20:50958503-50958851 | Common:1; Rare:113; Clinvar (benign):2 |