| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34112206-34112441 | Rare:70 | ||||
| chr20:34303281-34303495 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34363110-34363352 | Rare:69 | ||||
| chr20:34516303-34516451 | Common:3; Rare:58 | ||||
| chr20:34558532-34558760 | Common:1; Rare:59 | ||||
| chr20:34677074-34677320 | Rare:64 | ||||
| chr20:34704110-34704354 | Common:1; Rare:80 | ||||
| chr20:34872817-34872931 | Rare:42 | ||||
| chr20:34876271-34876648 | Common:3; Rare:104 | ||||
| chr20:34955720-34955841 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147074-35147437 | Common:2; Rare:129 | ||||
| chr20:35171765-35172140 | Common:2; Rare:82 | ||||
| chr20:35226444-35226664 | Rare:49 | ||||
| chr20:35284464-35284889 | Common:3; Rare:127 | ||||
| chr20:35411945-35412087 | Rare:53 |