| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45812339-45812794 | Common:5; Rare:134 | ||||
| chr20:45833576-45833852 | Common:4; Rare:60 | ||||
| chr20:45834076-45834180 | Rare:38 | ||||
| chr20:45857320-45857633 | Common:3; Rare:88 | ||||
| chr20:45891069-45891200 | Common:2; Rare:35; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:45891204-45891410 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45896227-45896269 | Common:2; Rare:30 | ||||
| chr20:45897017-45897201 | Common:1; Rare:35 | ||||
| chr20:45910893-45911250 | Common:4; Rare:109 | ||||
| chr20:45934654-45934724 | Rare:31 | ||||
| chr20:45935045-45935329 | Rare:113 | ||||
| chr20:46364366-46364520 | Rare:56 | ||||
| chr20:46406571-46406787 | Common:2; Rare:57 | ||||
| chr20:46513536-46513596 | Common:1; Rare:18 | ||||
| chr20:47356660-47356849 | Rare:43 |