| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45416035-45416159 | Rare:34 | ||||
| chr20:45791854-45792014 | Common:1; Rare:61 | ||||
| chr20:45812951-45813024 | Common:1; Rare:12 | ||||
| chr20:45857342-45857639 | Common:3; Rare:80 | ||||
| chr20:45891020-45891387 | Common:3; Rare:109; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45934644-45934725 | Rare:39 | ||||
| chr20:46406571-46406787 | Common:2; Rare:57 | ||||
| chr20:47318384-47318587 | Rare:45 | ||||
| chr20:47318997-47319114 | Common:1; Rare:31 | ||||
| chr20:47356661-47356913 | Rare:62 | ||||
| chr20:47501730-47502009 | Common:1; Rare:98 | ||||
| chr20:49046179-49046363 | Common:3; Rare:56 | ||||
| chr20:49278031-49278241 | Rare:56 | ||||
| chr20:50113112-50113221 | Common:5; Rare:53 | ||||
| chr20:50115899-50116104 | Common:3; Rare:51 |