| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44885415-44885812 | Common:7; Rare:125 | ||||
| chr20:45363366-45363527 | Common:1; Rare:40 | ||||
| chr20:45416038-45416159 | Rare:33 | ||||
| chr20:45791920-45791996 | Rare:29 | ||||
| chr20:45812351-45812698 | Common:3; Rare:103 | ||||
| chr20:45857350-45857633 | Common:3; Rare:73 | ||||
| chr20:45891291-45891379 | Rare:35; Clinvar:2 | ||||
| chr20:45912143-45912175 | Rare:7 | ||||
| chr20:45934564-45934707 | Common:1; Rare:73 | ||||
| chr20:45935045-45935333 | Rare:113 | ||||
| chr20:46118131-46118344 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:46364362-46364588 | Common:1; Rare:85 | ||||
| chr20:46406571-46406782 | Common:2; Rare:52 | ||||
| chr20:46513485-46513620 | Common:1; Rare:42 | ||||
| chr20:47356678-47356899 | Rare:55 |