| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10434130-10434239 | Common:2; Rare:44; Clinvar (benign):1 | ||||
| chr20:13784878-13785100 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995246-13995603 | Rare:102 | ||||
| chr20:16573299-16573540 | Common:1; Rare:66 | ||||
| chr20:17569973-17570202 | Common:3; Rare:100 | ||||
| chr20:17968442-17968579 | Common:3; Rare:60 | ||||
| chr20:17968784-17969129 | Common:3; Rare:122 | ||||
| chr20:18467010-18467109 | Rare:25 | ||||
| chr20:18467137-18467439 | Common:1; Rare:64 | ||||
| chr20:18497158-18497308 | Common:1; Rare:56 | ||||
| chr20:18567303-18567499 | Common:2; Rare:71 | ||||
| chr20:20017242-20017399 | Rare:57 | ||||
| chr20:21303261-21303368 | Rare:46 | ||||
| chr20:23350589-23350861 | Common:1; Rare:93 | ||||
| chr20:23421400-23421630 | Common:4; Rare:100 |