| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45934536-45934730 | Common:1; Rare:92 | ||||
| chr20:46406565-46406793 | Common:2; Rare:62 | ||||
| chr20:47318993-47319024 | Rare:8 | ||||
| chr20:47356675-47356882 | Rare:47 | ||||
| chr20:47501710-47502000 | Common:1; Rare:100 | ||||
| chr20:49046115-49046379 | Common:3; Rare:83 | ||||
| chr20:49278037-49278256 | Rare:58 | ||||
| chr20:49812645-49812925 | Common:2; Rare:72 | ||||
| chr20:49915468-49915829 | Common:4; Rare:110 | ||||
| chr20:50113124-50113292 | Common:6; Rare:72 | ||||
| chr20:50794853-50795099 | Common:1; Rare:90 | ||||
| chr20:50958515-50958853 | Common:1; Rare:107; Clinvar (benign):1 | ||||
| chr20:51802338-51802781 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:56392123-56392696 | Common:6; Rare:154 | ||||
| chr20:58650926-58651313 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):1 |