| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:1491333-1491633 | Common:2; Rare:72 | ||||
| chr20:1588640-1588826 | Rare:1 | ||||
| chr20:1895295-1895448 | Common:1; Rare:43 | ||||
| chr20:2101701-2101845 | Rare:35 | ||||
| chr20:2102068-2102273 | Common:3; Rare:61 | ||||
| chr20:2508872-2509213 | Common:1; Rare:67 | ||||
| chr20:2652400-2652655 | Common:9; Rare:94 | ||||
| chr20:2652980-2653297 | Common:4; Rare:97; Clinvar (benign):1 | ||||
| chr20:2664175-2664284 | Common:3; Rare:46 | ||||
| chr20:2840624-2840777 | Common:1; Rare:62 | ||||
| chr20:2873357-2873477 | Common:1; Rare:38 | ||||
| chr20:3209244-3209342 | Common:1; Rare:15 | ||||
| chr20:3209424-3209542 | Common:1; Rare:41 | ||||
| chr20:3407901-3408024 | Rare:33 | ||||
| chr20:3732552-3732780 | Rare:50 |