| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44746226-44746402 | Common:1; Rare:36 | ||||
| chr20:44960345-44960564 | Common:1; Rare:85 | ||||
| chr20:44966357-44966588 | Common:2; Rare:91 | ||||
| chr20:45348332-45348595 | Common:2; Rare:82 | ||||
| chr20:45363357-45363595 | Common:2; Rare:65 | ||||
| chr20:45406541-45406938 | Rare:97 | ||||
| chr20:45407067-45407337 | Common:1; Rare:42 | ||||
| chr20:45407404-45407489 | Rare:17 | ||||
| chr20:45416038-45416189 | Rare:56; Clinvar:1 | ||||
| chr20:45791913-45792014 | Common:1; Rare:39 | ||||
| chr20:45833278-45833477 | Common:1; Rare:34 | ||||
| chr20:45834044-45834249 | Rare:75 | ||||
| chr20:45857286-45857634 | Common:4; Rare:102 | ||||
| chr20:45891227-45891387 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912136-45912314 | Common:3; Rare:39 |