| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45891258-45891379 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934622-45934730 | Rare:54 | ||||
| chr20:45935056-45935358 | Rare:117 | ||||
| chr20:45972172-45972444 | Rare:110 | ||||
| chr20:46364362-46364523 | Rare:61 | ||||
| chr20:46406578-46406782 | Common:1; Rare:50 | ||||
| chr20:47356668-47356927 | Rare:63 | ||||
| chr20:47501717-47502005 | Common:1; Rare:101 | ||||
| chr20:48921575-48921826 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:49046166-49046358 | Common:3; Rare:57 | ||||
| chr20:49046650-49046873 | Common:3; Rare:80 | ||||
| chr20:49219191-49219482 | Common:1; Rare:128 | ||||
| chr20:49278037-49278259 | Rare:59 | ||||
| chr20:49812765-49812927 | Common:3; Rare:44 | ||||
| chr20:49936255-49936412 | Rare:64 |