| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1801300-1801463 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422316-5422665 | Common:3; Rare:113 | ||||
| chr5:6378479-6378674 | Rare:81 | ||||
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr5:10249874-10250170 | Common:16; Rare:141 | ||||
| chr5:10353573-10353925 | Common:3; Rare:134 | ||||
| chr5:11903170-11903322 | Rare:28 | ||||
| chr5:11903367-11903548 | Rare:26 | ||||
| chr5:16465715-16465895 | Rare:32 | ||||
| chr5:16713600-16713770 | Common:1; Rare:39 | ||||
| chr5:16741844-16741996 | Common:1; Rare:26 | ||||
| chr5:17216215-17216365 | Rare:25 | ||||
| chr5:17217001-17217058 | Rare:8 | ||||
| chr5:24644684-24644898 | Common:5; Rare:39 | ||||
| chr5:27038501-27038755 | Rare:44 |