| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:443120-443269 | Common:8; Rare:61 | ||||
| chr5:693293-693586 | Common:6; Rare:87 | ||||
| chr5:892540-892586 | Rare:9 | ||||
| chr5:892653-892917 | Common:5; Rare:90 | ||||
| chr5:1799791-1799993 | Common:4; Rare:94 | ||||
| chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422388-5422689 | Common:2; Rare:99 | ||||
| chr5:6378479-6378686 | Rare:87 | ||||
| chr5:6632996-6633407 | Common:8; Rare:135; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7851092-7851272 | Common:1; Rare:42 | ||||
| chr5:7869000-7869223 | Common:2; Rare:114; Clinvar (benign):2 | ||||
| chr5:9546042-9546360 | Common:7; Rare:73 | ||||
| chr5:9546444-9546469 | Rare:5 | ||||
| chr5:10353564-10353901 | Common:4; Rare:133 | ||||
| chr5:14581651-14581856 | Rare:90 |