Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:43409145-43409450 | Common:3; Rare:101 | ||||
chr10:45727164-45727273 | Rare:42 | ||||
chr10:45972392-45972554 | Rare:50 | ||||
chr10:49539028-49539175 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr10:49941950-49942081 | Rare:31 | ||||
chr10:50739919-50739962 | Rare:9 | ||||
chr10:52314058-52314294 | Common:1; Rare:57 | ||||
chr10:68331916-68332111 | Common:1; Rare:85 | ||||
chr10:68407256-68407382 | Common:3; Rare:40 | ||||
chr10:68721090-68721259 | Common:1; Rare:52 | ||||
chr10:68901049-68901336 | Common:3; Rare:114 | ||||
chr10:68956093-68956222 | Rare:58 | ||||
chr10:71851204-71851422 | Common:5; Rare:97; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273653-72273942 | Rare:74 | ||||
chr10:73167988-73168142 | Rare:33 |