| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1930905-1931224 | Common:3; Rare:81 | ||||
| chr5:8457556-8457741 | Common:2; Rare:63 | ||||
| chr5:14358159-14358192 | Rare:11 | ||||
| chr5:43041491-43041755 | Common:3; Rare:44 | ||||
| chr5:43065741-43066036 | Common:3; Rare:48 | ||||
| chr5:43066889-43067043 | Rare:64 | ||||
| chr5:55354716-55354967 | Common:2; Rare:54 | ||||
| chr5:59771276-59771407 | Common:1; Rare:18 | ||||
| chr5:61360116-61360328 | Common:2; Rare:38 | ||||
| chr5:65925573-65925955 | Rare:147 | ||||
| chr5:66989714-66990037 | Common:1; Rare:44 | ||||
| chr5:67015318-67015443 | Rare:18 | ||||
| chr5:67257550-67257786 | Common:2; Rare:42 | ||||
| chr5:67646790-67647053 | Common:1; Rare:31 | ||||
| chr5:87369530-87369847 | Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 |