| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3159821-3159944 | Rare:42 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3682002-3682188 | Common:3; Rare:43 | ||||
| chr20:3767730-3768077 | Common:5; Rare:109 | ||||
| chr20:3820435-3820567 | Common:1; Rare:55 | ||||
| chr20:3846705-3846893 | Rare:57 | ||||
| chr20:4148575-4148907 | Rare:90 | ||||
| chr20:4686229-4686485 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr20:5112883-5113194 | Common:1; Rare:122 | ||||
| chr20:5119874-5120174 | Common:1; Rare:101 | ||||
| chr20:5610865-5611170 | Common:2; Rare:106 | ||||
| chr20:5950414-5950695 | Common:8; Rare:86 | ||||
| chr20:13638904-13639003 | Common:1; Rare:24 | ||||
| chr20:13784893-13785080 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr20:16573308-16573567 | Common:1; Rare:73 |