| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56468329-56468761 | Rare:133 | ||||
| chr20:57709883-57710301 | Common:1; Rare:118 | ||||
| chr20:58309418-58309819 | Common:3; Rare:167 | ||||
| chr20:58515390-58515507 | Common:2; Rare:21 | ||||
| chr20:58652313-58652429 | Common:2; Rare:50 | ||||
| chr20:58888773-58888836 | Rare:22 | ||||
| chr20:58890930-58891445 | Common:6; Rare:214 | ||||
| chr20:58891913-58892171 | Common:5; Rare:126 | ||||
| chr20:58903523-58903771 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:58909126-58909219 | Common:1; Rare:29; Clinvar:1 | ||||
| chr20:58909331-58909802 | Rare:103; Clinvar (pathogenic):6 | ||||
| chr20:58909929-58910405 | Rare:111 | ||||
| chr20:59933632-59933798 | Common:4; Rare:66 | ||||
| chr20:59940238-59940507 | Rare:104 | ||||
| chr20:62065867-62066054 | Common:2; Rare:79 |