| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915450-34915744 | Common:1; Rare:72 | ||||
| chr5:35230329-35230351 | Rare:6 | ||||
| chr5:35617739-35617989 | Common:1; Rare:61 | ||||
| chr5:35856725-35856933 | Rare:31 | ||||
| chr5:36151874-36152120 | Rare:68 | ||||
| chr5:36241571-36241961 | Common:5; Rare:138; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36606411-36606668 | Rare:45 | ||||
| chr5:36876636-36876914 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371062-37371389 | Common:2; Rare:75 | ||||
| chr5:38556440-38556809 | Common:3; Rare:126 | ||||
| chr5:38557225-38557375 | Rare:40 | ||||
| chr5:38557436-38557533 | Rare:19 | ||||
| chr5:38845718-38846096 | Common:2; Rare:98 | ||||
| chr5:39074333-39074489 | Common:1; Rare:74 | ||||
| chr5:39424929-39425322 | Common:3; Rare:80 |