| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46406578-46406727 | Common:1; Rare:32 | ||||
| chr20:46513523-46513602 | Common:1; Rare:27 | ||||
| chr20:46709592-46709713 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:47319034-47319140 | Common:1; Rare:36 | ||||
| chr20:47356664-47356927 | Rare:64 | ||||
| chr20:47501698-47501993 | Common:1; Rare:103 | ||||
| chr20:49219258-49219518 | Common:1; Rare:118 | ||||
| chr20:49278036-49278288 | Rare:70 | ||||
| chr20:49812542-49812870 | Common:2; Rare:69 | ||||
| chr20:49915487-49915574 | Common:2; Rare:30 | ||||
| chr20:49936278-49936429 | Rare:63 | ||||
| chr20:50112820-50113244 | Common:6; Rare:152 | ||||
| chr20:50115899-50116117 | Common:3; Rare:53 | ||||
| chr20:50153639-50153893 | Common:2; Rare:100 | ||||
| chr20:50958461-50958857 | Common:1; Rare:148; Clinvar:4; Clinvar (benign):4 |