| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70403965-70404210 | Rare:89 | ||||
| chr10:70404748-70404830 | Common:1; Rare:16 | ||||
| chr10:70478469-70478951 | Rare:146 | ||||
| chr10:70815786-70816059 | Rare:98 | ||||
| chr10:70887852-70888052 | Common:1; Rare:39 | ||||
| chr10:70888186-70888319 | Common:1; Rare:27 | ||||
| chr10:70888525-70888718 | Common:2; Rare:60; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:71319048-71319361 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71773429-71773711 | Common:4; Rare:87 | ||||
| chr10:71851150-71851506 | Common:5; Rare:134; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:72215841-72216415 | Rare:198 | ||||
| chr10:72216422-72216544 | Common:3; Rare:22 | ||||
| chr10:72217095-72217179 | Rare:24 | ||||
| chr10:72273649-72274131 | Common:1; Rare:133 | ||||
| chr10:72274372-72274715 | Common:2; Rare:101 |