| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34008020-34008214 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656164-34656473 | Common:3; Rare:79 | ||||
| chr5:34686787-34686945 | Common:1; Rare:28 | ||||
| chr5:34839264-34839420 | Common:2; Rare:47 | ||||
| chr5:34929501-34929845 | Rare:129 | ||||
| chr5:35617569-35617928 | Common:1; Rare:65 | ||||
| chr5:36151794-36152145 | Rare:84 | ||||
| chr5:36241565-36241875 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36876623-36876915 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877047-36877173 | Rare:44; Clinvar:1 | ||||
| chr5:37371031-37371197 | Rare:62 | ||||
| chr5:37379084-37379498 | Common:3; Rare:122 | ||||
| chr5:38557204-38557308 | Rare:26 | ||||
| chr5:38557436-38557484 | Rare:9 | ||||
| chr5:38845739-38846053 | Common:2; Rare:83 |