| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151881-36152174 | Rare:91 | ||||
| chr5:36241632-36241765 | Rare:35; Clinvar (benign):1 | ||||
| chr5:36242163-36242334 | Common:1; Rare:44 | ||||
| chr5:36876636-36876889 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877103-36877161 | Rare:22 | ||||
| chr5:37371053-37371132 | Rare:32 | ||||
| chr5:37379080-37379386 | Common:3; Rare:83 | ||||
| chr5:38556472-38556841 | Common:3; Rare:127 | ||||
| chr5:38557183-38557428 | Rare:66 | ||||
| chr5:38557452-38557488 | Rare:7 | ||||
| chr5:38595396-38595532 | Common:1; Rare:12 | ||||
| chr5:38845712-38846053 | Common:2; Rare:89 | ||||
| chr5:39074363-39074541 | Common:1; Rare:84 | ||||
| chr5:40679678-40679929 | Common:2; Rare:55 | ||||
| chr5:40755831-40756089 | Rare:64 |