| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:40687838-40687986 | Rare:53; Clinvar:1 | ||||
| chr20:40688188-40688580 | Rare:122; Clinvar:2 | ||||
| chr20:43682044-43682378 | Common:3; Rare:55 | ||||
| chr20:44585660-44585867 | Common:1; Rare:45 | ||||
| chr20:44598537-44598701 | Common:2; Rare:24 | ||||
| chr20:44671685-44671816 | Common:2; Rare:33 | ||||
| chr20:45899002-45899315 | Rare:66 | ||||
| chr20:45902265-45902543 | Common:1; Rare:95 | ||||
| chr20:45971552-45971638 | Rare:24 | ||||
| chr20:46010622-46010953 | Common:1; Rare:90 | ||||
| chr20:46011737-46011976 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr20:46399489-46399680 | Rare:32 | ||||
| chr20:47317356-47317528 | Common:1; Rare:35 | ||||
| chr20:47352505-47352602 | Rare:16 | ||||
| chr20:47357542-47357663 | Common:1; Rare:19 |