| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45934618-45934707 | Rare:46 | ||||
| chr20:46363926-46364055 | Common:1; Rare:23 | ||||
| chr20:46364369-46364570 | Common:1; Rare:75 | ||||
| chr20:46406565-46406790 | Common:2; Rare:61 | ||||
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:47501761-47502002 | Common:1; Rare:83 | ||||
| chr20:49046141-49046358 | Common:3; Rare:64 | ||||
| chr20:49219200-49219481 | Common:1; Rare:126 | ||||
| chr20:49915521-49915575 | Common:2; Rare:15 | ||||
| chr20:49936246-49936410 | Rare:64 | ||||
| chr20:50113124-50113226 | Common:5; Rare:49 | ||||
| chr20:50115926-50116077 | Common:1; Rare:35 | ||||
| chr20:50794824-50795106 | Common:2; Rare:97 | ||||
| chr20:50958509-50958845 | Common:1; Rare:106; Clinvar (benign):2 | ||||
| chr20:56392187-56392678 | Common:6; Rare:128 |