| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47356646-47356892 | Rare:60 | ||||
| chr20:47501752-47502009 | Common:1; Rare:90 | ||||
| chr20:47786514-47786827 | Common:7; Rare:54 | ||||
| chr20:49046179-49046421 | Common:3; Rare:74 | ||||
| chr20:49219197-49219454 | Common:1; Rare:115 | ||||
| chr20:49278026-49278269 | Rare:65 | ||||
| chr20:49915470-49915582 | Common:3; Rare:41 | ||||
| chr20:50113117-50113263 | Common:5; Rare:70 | ||||
| chr20:50115926-50116080 | Common:1; Rare:36 | ||||
| chr20:50153634-50153893 | Common:2; Rare:102 | ||||
| chr20:50510159-50510454 | Common:3; Rare:116 | ||||
| chr20:50958471-50958892 | Common:1; Rare:163; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593797-53593926 | Common:1; Rare:51 | ||||
| chr20:56392187-56392465 | Common:1; Rare:82 | ||||
| chr20:58651040-58651305 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 |