| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46363926-46364087 | Common:1; Rare:31 | ||||
| chr20:46364362-46364551 | Rare:72 | ||||
| chr20:46406546-46406818 | Common:4; Rare:75 | ||||
| chr20:46513485-46513620 | Common:1; Rare:42 | ||||
| chr20:46651301-46651396 | Rare:32 | ||||
| chr20:46689184-46689299 | Rare:46; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr20:46709392-46709695 | Common:2; Rare:84; Clinvar:1 | ||||
| chr20:47348067-47348307 | Common:1; Rare:32 | ||||
| chr20:47355600-47355893 | Rare:55 | ||||
| chr20:47356646-47356872 | Rare:50 | ||||
| chr20:47501737-47502132 | Common:1; Rare:129 | ||||
| chr20:47786530-47786570 | Common:1; Rare:9 | ||||
| chr20:48921575-48921856 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:49046104-49046423 | Common:3; Rare:94 | ||||
| chr20:49046665-49046860 | Common:3; Rare:68 |