| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:5422366-5422710 | Common:2; Rare:116 | ||||
| chr5:6632982-6633460 | Common:8; Rare:154; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868987-7869209 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr5:10353445-10353920 | Common:4; Rare:166 | ||||
| chr5:10761127-10761411 | Common:9; Rare:94 | ||||
| chr5:14581643-14581855 | Rare:89 | ||||
| chr5:16616964-16617218 | Common:2; Rare:72; Clinvar (benign):6 | ||||
| chr5:31532002-31532341 | Common:3; Rare:90 | ||||
| chr5:32174252-32174428 | Common:2; Rare:65 | ||||
| chr5:33440624-33441058 | Common:6; Rare:114 | ||||
| chr5:34915491-34915764 | Common:1; Rare:72 | ||||
| chr5:34929585-34929908 | Rare:114 | ||||
| chr5:36876650-36876887 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371053-37371421 | Common:2; Rare:92 | ||||
| chr5:40679697-40679960 | Common:1; Rare:59 |