| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70403940-70404197 | Common:1; Rare:97 | ||||
| chr10:70478624-70479009 | Common:1; Rare:128 | ||||
| chr10:70815783-70815999 | Common:1; Rare:78 | ||||
| chr10:70816297-70816471 | Rare:39 | ||||
| chr10:70887871-70888121 | Common:1; Rare:53 | ||||
| chr10:70888549-70888733 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:71319057-71319344 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71773442-71773673 | Common:3; Rare:77 | ||||
| chr10:71851164-71851440 | Common:5; Rare:117; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:71964089-71964236 | Common:1; Rare:43 | ||||
| chr10:72215902-72216176 | Rare:96 | ||||
| chr10:72216206-72216427 | Rare:82 | ||||
| chr10:72273642-72274107 | Rare:131 | ||||
| chr10:72274400-72274707 | Common:2; Rare:89 | ||||
| chr10:72354528-72354802 | Common:1; Rare:84 |