| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17968376-17968646 | Common:5; Rare:117 | ||||
| chr20:17968699-17969581 | Common:5; Rare:248 | ||||
| chr20:18137787-18138103 | Common:3; Rare:119 | ||||
| chr20:18467148-18467492 | Common:3; Rare:81 | ||||
| chr20:18507346-18507616 | Common:1; Rare:76; Clinvar:1 | ||||
| chr20:18567497-18567601 | Rare:32 | ||||
| chr20:19886466-19886589 | Rare:33 | ||||
| chr20:19889001-19889230 | Common:1; Rare:38 | ||||
| chr20:20017211-20017418 | Rare:76 | ||||
| chr20:21303118-21303472 | Rare:112 | ||||
| chr20:21303703-21303846 | Rare:44 | ||||
| chr20:23350456-23350890 | Common:4; Rare:137 | ||||
| chr20:23361832-23362198 | Common:4; Rare:124 | ||||
| chr20:23421400-23421630 | Common:4; Rare:100 | ||||
| chr20:23637892-23638085 | Common:5; Rare:63; Clinvar (benign):1 |