| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10434130-10434288 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr20:10434645-10434721 | Common:1; Rare:35 | ||||
| chr20:10434987-10435487 | Rare:136 | ||||
| chr20:10673931-10674549 | Common:5; Rare:189; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:13638830-13639093 | Common:2; Rare:84 | ||||
| chr20:13784802-13785128 | Common:3; Rare:142; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13785320-13785393 | Rare:30 | ||||
| chr20:15985271-15985568 | Common:5; Rare:58 | ||||
| chr20:15985985-15986214 | Common:1; Rare:39 | ||||
| chr20:16573300-16573597 | Common:2; Rare:87 | ||||
| chr20:16729795-16730116 | Common:3; Rare:99 | ||||
| chr20:17569971-17570167 | Common:3; Rare:83 | ||||
| chr20:17682171-17682673 | Common:5; Rare:163 | ||||
| chr20:17968414-17969119 | Common:9; Rare:274 | ||||
| chr20:17969265-17969458 | Rare:43 |