| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45416362-45416673 | Rare:156; Clinvar (pathogenic):4 | ||||
| chr20:45791878-45792018 | Common:2; Rare:102 | ||||
| chr20:45812296-45812797 | Common:8; Rare:247 | ||||
| chr20:45833709-45833852 | Common:6; Rare:60 | ||||
| chr20:45833855-45834207 | Common:4; Rare:102 | ||||
| chr20:45857302-45857639 | Common:8; Rare:190 | ||||
| chr20:45881009-45881264 | Common:4; Rare:112 | ||||
| chr20:45891197-45891435 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):2 | ||||
| chr20:45910750-45911320 | Common:10; Rare:229 | ||||
| chr20:45934190-45934520 | Common:6; Rare:120 | ||||
| chr20:45934613-45934753 | Rare:137 | ||||
| chr20:45934937-45935400 | Common:3; Rare:343 | ||||
| chr20:45971716-45972073 | Common:6; Rare:168 | ||||
| chr20:45972130-45972750 | Common:6; Rare:303 | ||||
| chr20:46363660-46364120 | Common:2; Rare:135 |