| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62952551-62953127 | Common:14; Rare:337; Clinvar (pathogenic):2 | ||||
| chr20:62962841-62963796 | Common:12; Rare:407 | ||||
| chr20:63216057-63216421 | Common:4; Rare:231 | ||||
| chr20:63235577-63235933 | Common:3; Rare:86 | ||||
| chr20:63272688-63272931 | Common:8; Rare:143 | ||||
| chr20:63283832-63284586 | Common:5; Rare:268 | ||||
| chr20:63284625-63285031 | Common:5; Rare:300 | ||||
| chr20:63520623-63520784 | Common:2; Rare:72 | ||||
| chr20:63574217-63574363 | Common:1; Rare:37 | ||||
| chr20:63619251-63619801 | Common:3; Rare:245 | ||||
| chr20:63626722-63626889 | Rare:140 | ||||
| chr20:63627011-63627298 | Rare:206 | ||||
| chr20:63652376-63652874 | Common:1; Rare:125 | ||||
| chr20:63653330-63653627 | Common:2; Rare:79 | ||||
| chr20:63657636-63657846 | Common:14; Rare:77 |