| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185504480-185504664 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:282743-282852 | Common:1; Rare:9 | ||||
| chr5:784685-784880 | Common:5; Rare:61 | ||||
| chr5:912447-912565 | Common:3; Rare:33 | ||||
| chr5:1042794-1043085 | Common:32; Rare:103 | ||||
| chr5:1052411-1052529 | Common:1; Rare:43 | ||||
| chr5:1474559-1474778 | Rare:78 | ||||
| chr5:1475093-1475107 | Rare:3 | ||||
| chr5:1476435-1476760 | Common:2; Rare:63 | ||||
| chr5:1477289-1477494 | Common:1; Rare:64 | ||||
| chr5:1516442-1516454 | Rare:1 | ||||
| chr5:1548294-1548555 | Common:1; Rare:45 | ||||
| chr5:1551561-1551750 | Common:2; Rare:46 | ||||
| chr5:1555263-1555486 | Common:1; Rare:46 | ||||
| chr5:1578267-1578424 | Common:3; Rare:29 |