| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53608821-53608943 | Rare:20 | ||||
| chr20:54207814-54207829 | Rare:4 | ||||
| chr20:54207838-54208447 | Common:2; Rare:164 | ||||
| chr20:56392140-56392708 | Common:6; Rare:153 | ||||
| chr20:56468397-56468700 | Rare:107 | ||||
| chr20:56524584-56524802 | Common:1; Rare:49 | ||||
| chr20:56533107-56533278 | Common:3; Rare:25 | ||||
| chr20:57329619-57329939 | Common:1; Rare:151 | ||||
| chr20:57351429-57351580 | Rare:43 | ||||
| chr20:57525075-57525459 | Common:5; Rare:86 | ||||
| chr20:58150865-58150973 | Rare:47 | ||||
| chr20:58228504-58228824 | Common:3; Rare:95 | ||||
| chr20:58309418-58309687 | Common:2; Rare:105 | ||||
| chr20:58388998-58389277 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651113-58651390 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 |