chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141542402515424026CA54GENICheterozygous795631821
141542409115424092GA65GENICheterozygous795631822
141542409615424097CA61GENICheterozygous795631823
141542409715424098CG61GENICheterozygous795631824
141542415215424153TC83GENICheterozygous795631825
141542421115424212CT131GENICheterozygous795631826
141542425015424251GC117GENICheterozygous795631827
141542426415424265CT105GENICheterozygous795631828
141542427015424271TC109GENICheterozygous795631829
141542427615424277AG114GENICheterozygous795631830
141542430515424306CT145GENICheterozygous795631831
141542431415424315GT145GENICheterozygous795631832
141542433615424337AT155GENICheterozygous795631833
141542435915424360GT161GENICheterozygous795631834
141542436115424362GA161GENICheterozygous795631835
141542439315424394GA133GENICheterozygous795631836
141542442815424429AC89GENICheterozygous795631837
141542442915424430GT88GENICheterozygous795631838
141542444915424450TG70GENICpossibly homozygous795631839
141542446715424468GA65GENICheterozygous795631840
141542450215424503CG55GENICheterozygous795631841
141542451215424513TG53GENICheterozygous795631842