| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50267382-50267546 | Common:4; Rare:28 | ||||
| chr20:50276131-50276342 | Common:1; Rare:40 | ||||
| chr20:50292582-50292765 | Common:2; Rare:40 | ||||
| chr20:50346652-50346782 | Common:1; Rare:23 | ||||
| chr20:50389604-50389699 | Rare:15 | ||||
| chr20:50415681-50415940 | Common:1; Rare:76 | ||||
| chr20:52973333-52973634 | Rare:82 | ||||
| chr20:53077650-53077941 | Common:1; Rare:49 | ||||
| chr20:56003981-56004265 | Common:1; Rare:85 | ||||
| chr20:57629413-57629688 | Common:2; Rare:70 | ||||
| chr20:58905182-58905475 | Common:2; Rare:54; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:62306373-62306733 | Common:3; Rare:132 | ||||
| chr20:63832246-63832552 | Common:2; Rare:80 | ||||
| chr20:63873485-63873686 | Common:2; Rare:42 | ||||
| chr21:15444154-15444462 | Common:3; Rare:52 |