| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35699096-35699719 | Rare:266; Clinvar (benign):6 | ||||
| chr20:35740865-35741910 | Common:16; Rare:580 | ||||
| chr20:35742160-35742675 | Common:12; Rare:333 | ||||
| chr20:35772123-35772523 | Common:1; Rare:178 | ||||
| chr20:36154434-36154882 | Rare:149 | ||||
| chr20:36236393-36236542 | Common:1; Rare:66 | ||||
| chr20:36461144-36461513 | Common:2; Rare:186 | ||||
| chr20:36541391-36541555 | Common:4; Rare:84 | ||||
| chr20:36573196-36573749 | Common:4; Rare:386 | ||||
| chr20:36574394-36574630 | Rare:141 | ||||
| chr20:36605484-36606051 | Common:5; Rare:327 | ||||
| chr20:36746044-36746223 | Common:4; Rare:134 | ||||
| chr20:36773707-36773978 | Common:5; Rare:142 | ||||
| chr20:36863834-36864161 | Common:1; Rare:85 | ||||
| chr20:36951576-36951925 | Common:2; Rare:202; Clinvar:3; Clinvar (benign):8 |