| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31674988-31675124 | Rare:24 | ||||
| chr20:32141659-32141889 | Common:3; Rare:67 | ||||
| chr20:32453422-32453650 | Common:1; Rare:61 | ||||
| chr20:32475287-32475628 | Common:1; Rare:77 | ||||
| chr20:34090572-34090626 | Rare:7 | ||||
| chr20:34093707-34093807 | Rare:25 | ||||
| chr20:34096748-34096913 | Rare:36 | ||||
| chr20:34103460-34103713 | Common:1; Rare:43 | ||||
| chr20:34540869-34541129 | Rare:55 | ||||
| chr20:34709157-34709309 | Common:2; Rare:64 | ||||
| chr20:34932001-34932267 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:35007852-35007980 | Common:1; Rare:28 | ||||
| chr20:35263732-35263825 | Rare:14 | ||||
| chr20:35476201-35476506 | Rare:56 | ||||
| chr20:35490972-35491241 | Common:2; Rare:57 |