| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3239152-3239329 | Common:1; Rare:64 | ||||
| chr20:3239557-3239719 | Common:1; Rare:47 | ||||
| chr20:3407565-3407742 | Common:3; Rare:48 | ||||
| chr20:3470883-3471039 | Common:2; Rare:69 | ||||
| chr20:3767720-3767906 | Common:1; Rare:57 | ||||
| chr20:3820468-3820576 | Rare:45 | ||||
| chr20:3889160-3889396 | Common:1; Rare:121; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4148615-4148867 | Rare:71 | ||||
| chr20:5112862-5113161 | Common:1; Rare:109 | ||||
| chr20:5119914-5120138 | Common:1; Rare:75 | ||||
| chr20:5126546-5127081 | Common:4; Rare:172 | ||||
| chr20:5950372-5950695 | Common:8; Rare:100 | ||||
| chr20:6122931-6123133 | Common:3; Rare:53; Clinvar:4; Clinvar (benign):3 | ||||
| chr20:8019759-8019884 | Rare:40 | ||||
| chr20:10218727-10218857 | Rare:28 |