| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45935056-45935345 | Rare:111 | ||||
| chr20:45971710-45972167 | Common:4; Rare:135 | ||||
| chr20:46363930-46364084 | Common:1; Rare:29 | ||||
| chr20:46364354-46364551 | Rare:73 | ||||
| chr20:46406565-46406801 | Common:2; Rare:63 | ||||
| chr20:46513501-46513604 | Common:1; Rare:34 | ||||
| chr20:46709518-46709720 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:47318723-47319082 | Common:1; Rare:111 | ||||
| chr20:47356646-47356873 | Rare:51 | ||||
| chr20:47501575-47501733 | Common:1; Rare:39 | ||||
| chr20:47501735-47502121 | Common:1; Rare:127 | ||||
| chr20:48921595-48921903 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:49046148-49046391 | Common:3; Rare:76 | ||||
| chr20:49188119-49188277 | Common:1; Rare:49 | ||||
| chr20:49219200-49219541 | Common:1; Rare:143 |