| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:892520-893001 | Common:5; Rare:155 | ||||
| chr5:1799778-1799993 | Common:8; Rare:101 | ||||
| chr5:1801295-1801473 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:10249872-10250445 | Common:19; Rare:265; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353590-10353910 | Common:3; Rare:119 | ||||
| chr5:16465715-16465895 | Rare:32 | ||||
| chr5:31532045-31532356 | Common:3; Rare:87 | ||||
| chr5:32174267-32174389 | Common:1; Rare:46 | ||||
| chr5:32444662-32444988 | Common:1; Rare:112 | ||||
| chr5:33440632-33441117 | Common:7; Rare:139 | ||||
| chr5:34008027-34008231 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656144-34656462 | Common:3; Rare:82 | ||||
| chr5:34915218-34915348 | Rare:37 | ||||
| chr5:34915483-34915744 | Common:1; Rare:63 |