| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45416038-45416159 | Rare:33 | ||||
| chr20:45792456-45792521 | Common:1; Rare:10 | ||||
| chr20:45812306-45812616 | Common:3; Rare:76 | ||||
| chr20:45834076-45834213 | Rare:52 | ||||
| chr20:45857342-45857639 | Common:3; Rare:80 | ||||
| chr20:45891010-45891432 | Common:3; Rare:127; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45896739-45897022 | Common:1; Rare:71; Clinvar:1 | ||||
| chr20:45897433-45897800 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr20:45912143-45912209 | Common:1; Rare:14 | ||||
| chr20:45934612-45934774 | Common:1; Rare:81 | ||||
| chr20:45935050-45935351 | Rare:117 | ||||
| chr20:45971717-45971992 | Common:3; Rare:80 | ||||
| chr20:45972172-45972257 | Rare:38 | ||||
| chr20:46008603-46009062 | Common:8; Rare:122; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:46363890-46364099 | Common:1; Rare:45 |