| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:892607-892941 | Common:5; Rare:109 | ||||
| chr5:1799756-1799996 | Common:8; Rare:112 | ||||
| chr5:1801281-1801460 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422184-5422677 | Common:3; Rare:166 | ||||
| chr5:6378476-6378694 | Rare:92 | ||||
| chr5:6449067-6449134 | Rare:11 | ||||
| chr5:7851014-7851173 | Common:2; Rare:31 | ||||
| chr5:7868991-7869194 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr5:9545977-9546303 | Common:9; Rare:80 | ||||
| chr5:10249869-10250445 | Common:19; Rare:266; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353553-10353970 | Common:4; Rare:160 | ||||
| chr5:10441782-10441962 | Common:1; Rare:50 | ||||
| chr5:10761054-10761137 | Common:1; Rare:37 | ||||
| chr5:11588809-11588938 | Common:2; Rare:23 | ||||
| chr5:11903178-11903548 | Rare:65 |