| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241637570-241637704 | Common:1; Rare:77 | ||||
| chr2:241686781-241687173 | Common:4; Rare:117 | ||||
| chr20:381196-381354 | Common:2; Rare:40 | ||||
| chr20:1118458-1118671 | Common:3; Rare:68 | ||||
| chr20:2652430-2652635 | Common:6; Rare:66 | ||||
| chr20:3209438-3209530 | Rare:30 | ||||
| chr20:3846736-3846893 | Rare:46 | ||||
| chr20:3889156-3889419 | Common:1; Rare:139; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:5119884-5120185 | Common:1; Rare:100 | ||||
| chr20:5126569-5126759 | Common:2; Rare:53 | ||||
| chr20:13784894-13785062 | Common:2; Rare:69; Clinvar (benign):2 | ||||
| chr20:17968403-17968589 | Common:4; Rare:74 | ||||
| chr20:17968762-17969119 | Common:4; Rare:130 | ||||
| chr20:23086289-23086503 | Rare:47 | ||||
| chr20:25195601-25195780 | Common:2; Rare:60 |