| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5950391-5950689 | Common:8; Rare:89 | ||||
| chr20:10034838-10035097 | Common:5; Rare:100 | ||||
| chr20:13784871-13785080 | Common:2; Rare:93; Clinvar (benign):3 | ||||
| chr20:16573300-16573546 | Common:1; Rare:69 | ||||
| chr20:17569949-17570210 | Common:3; Rare:115 | ||||
| chr20:17968431-17968590 | Common:4; Rare:65 | ||||
| chr20:17968770-17969129 | Common:4; Rare:127 | ||||
| chr20:17969530-17969554 | Rare:3 | ||||
| chr20:18466997-18467109 | Rare:28 | ||||
| chr20:18467148-18467448 | Common:1; Rare:59 | ||||
| chr20:18507464-18507624 | Rare:41; Clinvar:1 | ||||
| chr20:19212459-19212539 | Common:1; Rare:30 | ||||
| chr20:19889289-19889584 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr20:19935023-19935140 | Common:3; Rare:34; Clinvar (benign):3 | ||||
| chr20:20017242-20017388 | Rare:52 |