| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5126538-5126814 | Common:3; Rare:78 | ||||
| chr20:5610904-5611188 | Common:2; Rare:103 | ||||
| chr20:5950328-5950695 | Common:8; Rare:112 | ||||
| chr20:6053901-6054199 | Common:3; Rare:45 | ||||
| chr20:8019759-8019930 | Rare:52 | ||||
| chr20:10034834-10035097 | Common:5; Rare:101 | ||||
| chr20:10218716-10218830 | Rare:23 | ||||
| chr20:10640791-10641185 | Rare:114; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:13784871-13785131 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:14337508-14337679 | Rare:39 | ||||
| chr20:16573278-16573540 | Common:1; Rare:75 | ||||
| chr20:17569949-17570210 | Common:3; Rare:115 | ||||
| chr20:17682061-17682307 | Common:2; Rare:72 | ||||
| chr20:17968398-17968594 | Common:4; Rare:77 | ||||
| chr20:17968770-17969129 | Common:4; Rare:127 |