| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44187095-44187373 | Common:3; Rare:65 | ||||
| chr20:44210745-44211020 | Common:4; Rare:97 | ||||
| chr20:44522015-44522243 | Common:2; Rare:70 | ||||
| chr20:44960366-44960444 | Common:1; Rare:32 | ||||
| chr20:44966341-44966531 | Common:1; Rare:75 | ||||
| chr20:45406519-45406717 | Rare:53 | ||||
| chr20:45791916-45792014 | Common:1; Rare:37 | ||||
| chr20:45812302-45812692 | Common:4; Rare:110 | ||||
| chr20:45827210-45827557 | Common:2; Rare:61 | ||||
| chr20:45827565-45827595 | Rare:5 | ||||
| chr20:45833250-45833386 | Common:1; Rare:18 | ||||
| chr20:45834014-45834200 | Rare:66 | ||||
| chr20:45857350-45857633 | Common:3; Rare:73 | ||||
| chr20:45890998-45891387 | Common:4; Rare:121; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45934548-45934725 | Common:1; Rare:85 |