| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231412421-231412576 | Common:2; Rare:24 | ||||
| chr2:231514362-231514574 | Common:5; Rare:84 | ||||
| chr2:241868164-241868327 | Common:2; Rare:31 | ||||
| chr2:241902607-241902926 | Common:2; Rare:63 | ||||
| chr2:242088415-242088721 | Common:13; Rare:114 | ||||
| chr20:3200062-3200425 | Common:1; Rare:101 | ||||
| chr20:3203935-3204064 | Common:2; Rare:31 | ||||
| chr20:3340552-3340736 | Common:2; Rare:57 | ||||
| chr20:3784849-3784993 | Rare:49 | ||||
| chr20:3785731-3786039 | Rare:90 | ||||
| chr20:3935468-3935666 | Rare:29 | ||||
| chr20:4822531-4822806 | Common:5; Rare:61 | ||||
| chr20:4936919-4937243 | Common:3; Rare:56 | ||||
| chr20:5823224-5823589 | Common:4; Rare:63 | ||||
| chr20:6079451-6079719 | Common:4; Rare:52; Clinvar:1; Clinvar (pathogenic):1 |