| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49278039-49278278 | Rare:67 | ||||
| chr20:50113115-50113241 | Common:5; Rare:61 | ||||
| chr20:50958490-50958840 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593797-53593894 | Common:1; Rare:35 | ||||
| chr20:56392182-56392692 | Common:6; Rare:134 | ||||
| chr20:56629062-56629320 | Common:1; Rare:75 | ||||
| chr20:58388987-58389277 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58515353-58515507 | Common:3; Rare:29 | ||||
| chr20:58651080-58651305 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:59032220-59032598 | Common:4; Rare:161; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042735-59042970 | Common:1; Rare:84 | ||||
| chr20:59835845-59836051 | Rare:47 | ||||
| chr20:59933630-59933779 | Common:4; Rare:58 | ||||
| chr20:59940129-59940481 | Common:1; Rare:138 | ||||
| chr20:62143307-62143812 | Common:6; Rare:214 |