| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70576012-70576684 | Common:7; Rare:172 | ||||
| chr10:70683252-70683908 | Common:6; Rare:133 | ||||
| chr10:70816490-70816929 | Rare:220 | ||||
| chr10:70981673-70982815 | Common:19; Rare:277 | ||||
| chr10:71217980-71218480 | Common:2; Rare:86 | ||||
| chr10:71266290-71266730 | Common:3; Rare:103 | ||||
| chr10:71333200-71333570 | Common:5; Rare:65 | ||||
| chr10:71372772-71373330 | Common:6; Rare:147 | ||||
| chr10:71377265-71377647 | Common:9; Rare:131 | ||||
| chr10:71643870-71644230 | Rare:99 | ||||
| chr10:71644298-71644664 | Rare:106 | ||||
| chr10:71644809-71645209 | Common:3; Rare:78 | ||||
| chr10:71645140-71645410 | Common:1; Rare:54 | ||||
| chr10:71666767-71667167 | Common:7; Rare:143 | ||||
| chr10:71693780-71695040 | Common:19; Rare:535; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 |