| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915215-34915381 | Rare:48 | ||||
| chr5:34915448-34915875 | Common:2; Rare:128 | ||||
| chr5:35617642-35617930 | Common:1; Rare:55 | ||||
| chr5:36151874-36152203 | Rare:104 | ||||
| chr5:36241591-36241759 | Rare:50; Clinvar (benign):1 | ||||
| chr5:36242133-36242334 | Common:1; Rare:53 | ||||
| chr5:36876625-36876889 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877103-36877154 | Rare:20 | ||||
| chr5:37248949-37249084 | Common:2; Rare:27 | ||||
| chr5:37249284-37249480 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371011-37371379 | Common:2; Rare:100 | ||||
| chr5:37379059-37379368 | Common:3; Rare:75 | ||||
| chr5:38845712-38846133 | Common:2; Rare:105 | ||||
| chr5:39074346-39074566 | Common:1; Rare:100 | ||||
| chr5:40679177-40679423 | Common:3; Rare:49 |