| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45406541-45406732 | Rare:49 | ||||
| chr20:45791879-45792014 | Common:1; Rare:51 | ||||
| chr20:45833292-45833603 | Common:1; Rare:53 | ||||
| chr20:45857343-45857634 | Common:3; Rare:77 | ||||
| chr20:45891194-45891387 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912138-45912281 | Common:3; Rare:32 | ||||
| chr20:45934369-45934731 | Common:2; Rare:151 | ||||
| chr20:45935045-45935333 | Rare:113 | ||||
| chr20:45971717-45971998 | Common:3; Rare:81 | ||||
| chr20:46364377-46364551 | Rare:66 | ||||
| chr20:46406565-46406790 | Common:2; Rare:61 | ||||
| chr20:47318703-47318874 | Rare:51 | ||||
| chr20:47319034-47319166 | Common:1; Rare:51 | ||||
| chr20:47356662-47356853 | Rare:42 | ||||
| chr20:47501752-47502009 | Common:1; Rare:90 |