| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2840653-2840766 | Common:1; Rare:49 | ||||
| chr20:3173526-3173722 | Common:1; Rare:66 | ||||
| chr20:3209432-3209542 | Common:1; Rare:37 | ||||
| chr20:3767716-3768052 | Common:4; Rare:107 | ||||
| chr20:3846684-3846886 | Rare:60 | ||||
| chr20:4148559-4148861 | Rare:83 | ||||
| chr20:5112838-5113178 | Common:2; Rare:121 | ||||
| chr20:5950408-5950696 | Common:8; Rare:89 | ||||
| chr20:11890641-11890897 | Common:2; Rare:95 | ||||
| chr20:13784893-13785080 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr20:16573293-16573556 | Common:1; Rare:75 | ||||
| chr20:17968429-17968590 | Common:4; Rare:66 | ||||
| chr20:17968784-17969118 | Common:3; Rare:120 | ||||
| chr20:18288438-18288564 | Rare:34 | ||||
| chr20:18467065-18467448 | Common:1; Rare:79 |