| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10218732-10218929 | Rare:42 | ||||
| chr20:13784884-13785091 | Common:2; Rare:96; Clinvar (benign):3 | ||||
| chr20:13995225-13995610 | Rare:112 | ||||
| chr20:16573308-16573540 | Common:1; Rare:63 | ||||
| chr20:17968426-17968589 | Common:4; Rare:66 | ||||
| chr20:17968786-17968956 | Common:2; Rare:73 | ||||
| chr20:18467121-18467428 | Rare:66 | ||||
| chr20:21303070-21303372 | Rare:104 | ||||
| chr20:23086314-23086490 | Rare:36 | ||||
| chr20:25247761-25248078 | Common:1; Rare:94 | ||||
| chr20:25696772-25697062 | Common:3; Rare:85 | ||||
| chr20:31475202-31475300 | Rare:22 | ||||
| chr20:31547280-31547438 | Rare:40 | ||||
| chr20:31739109-31739362 | Common:1; Rare:63 | ||||
| chr20:32207694-32207921 | Common:2; Rare:86 |