| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6632982-6633367 | Common:8; Rare:124; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868987-7869227 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:9546003-9546366 | Common:9; Rare:92 | ||||
| chr5:10249856-10250445 | Common:19; Rare:275; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10307570-10307666 | Common:1; Rare:21 | ||||
| chr5:10307670-10307715 | Rare:11 | ||||
| chr5:10353560-10353975 | Common:4; Rare:160 | ||||
| chr5:10761040-10761465 | Common:14; Rare:146 | ||||
| chr5:14581643-14581896 | Rare:110 | ||||
| chr5:14664572-14664914 | Common:4; Rare:141 | ||||
| chr5:16465694-16465915 | Common:1; Rare:47 | ||||
| chr5:31532032-31532359 | Common:3; Rare:93 | ||||
| chr5:32174247-32174421 | Common:1; Rare:65 | ||||
| chr5:32710533-32710768 | Common:1; Rare:54 | ||||
| chr5:32711128-32711321 | Rare:29 |