| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36548914-36549147 | Common:1; Rare:52 | ||||
| chr20:36611923-36612046 | Rare:31 | ||||
| chr20:36898449-36898629 | Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:36950860-36950945 | Rare:15 | ||||
| chr20:40686338-40686509 | Common:1; Rare:32; Clinvar (benign):2 | ||||
| chr20:40686549-40686720 | Rare:32; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:40687514-40687573 | Rare:9; Clinvar:1 | ||||
| chr20:40687576-40687739 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:40687752-40687836 | Rare:13; Clinvar (benign):1 | ||||
| chr20:40687899-40687986 | Rare:30 | ||||
| chr20:40688548-40688566 | Rare:5 | ||||
| chr20:41100992-41101352 | Common:1; Rare:71 | ||||
| chr20:41121458-41121788 | Common:1; Rare:73 | ||||
| chr20:41138669-41138915 | Common:1; Rare:47 | ||||
| chr20:44618008-44618323 | Common:4; Rare:54 |