| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:326967-327766 | Common:10; Rare:224 | ||||
| chr20:327834-327943 | Common:1; Rare:21 | ||||
| chr20:328168-328662 | Common:14; Rare:100 | ||||
| chr20:427061-427475 | Rare:79; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr20:489783-489990 | Common:1; Rare:32 | ||||
| chr20:2658344-2658450 | Rare:28 | ||||
| chr20:2796373-2796577 | Common:1; Rare:58 | ||||
| chr20:2836992-2837181 | Common:1; Rare:31 | ||||
| chr20:3035683-3035871 | Rare:60 | ||||
| chr20:3221084-3221200 | Common:2; Rare:15 | ||||
| chr20:3784400-3784662 | Rare:53 | ||||
| chr20:3785100-3785273 | Common:2; Rare:79 | ||||
| chr20:3811533-3811587 | Common:2; Rare:6 | ||||
| chr20:3916953-3917178 | Rare:58; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:4090859-4091039 | Common:1; Rare:23 |