| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651144-58651295 | Common:2; Rare:30; Clinvar (benign):1 | ||||
| chr20:58909115-58909421 | Common:3; Rare:82; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:58909681-58910401 | Common:1; Rare:157; Clinvar (pathogenic):2 | ||||
| chr20:59940212-59940481 | Rare:106 | ||||
| chr20:62143273-62143752 | Common:6; Rare:199 | ||||
| chr20:62182959-62183049 | Rare:20 | ||||
| chr20:62238232-62238583 | Common:1; Rare:97 | ||||
| chr20:62386974-62387136 | Common:3; Rare:67 | ||||
| chr20:62937883-62938193 | Common:2; Rare:114 | ||||
| chr20:63498181-63498444 | Common:4; Rare:62 | ||||
| chr20:63499056-63499353 | Common:2; Rare:70 | ||||
| chr20:63626974-63627243 | Rare:105 | ||||
| chr20:63653380-63653645 | Common:2; Rare:33 | ||||
| chr20:63658242-63658355 | Common:2; Rare:36 | ||||
| chr20:63707834-63708118 | Rare:83 |