| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17975582-17975704 | Rare:40; Clinvar (benign):1 | ||||
| chr20:18295446-18295478 | Rare:9 | ||||
| chr20:18300657-18300841 | Rare:30 | ||||
| chr20:18388884-18389122 | Common:1; Rare:38 | ||||
| chr20:18489952-18490138 | Common:3; Rare:48 | ||||
| chr20:18782772-18782880 | Rare:13 | ||||
| chr20:19714386-19714399 | Rare:2 | ||||
| chr20:19757478-19757716 | Common:3; Rare:69 | ||||
| chr20:19757975-19758121 | Common:1; Rare:53 | ||||
| chr20:19758179-19758314 | Common:2; Rare:36 | ||||
| chr20:19786341-19786660 | Common:2; Rare:60 | ||||
| chr20:19815504-19815826 | Common:2; Rare:58 | ||||
| chr20:19817102-19817364 | Common:3; Rare:45 | ||||
| chr20:19888655-19888727 | Common:1; Rare:8 | ||||
| chr20:19890201-19890669 | Common:2; Rare:66 |