chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53317613933176140CT43GENIChomozygous793822689
53317653933176540TC34GENICheterozygous793822690
53317705133177052AC35GENIChomozygous793822691
53317727233177273CT55GENICheterozygous793822692
53317740033177401TC39GENICheterozygous793822693
53317758533177586TC58GENICheterozygous793822694
53317764233177643GA62GENICheterozygous793822695
53317766833177669CA63GENICheterozygous793822696
53317775133177752GT82GENICheterozygous793822697
53317777633177777TC89GENICheterozygous793822698
53317785333177854AG57GENICheterozygous793822699
53317799433177995GA60GENICheterozygous793822700
53317800733178008GA59GENICheterozygous793822701
53317807633178077CA66GENICheterozygous793822702
53317808033178081GA64GENICheterozygous793822703
53317808333178084GA64GENICheterozygous793822704
53317811233178113GA60GENICheterozygous793822705
53317815933178160CT49GENICheterozygous793822706
53317867833178679GC88GENICheterozygous793822707
53317867933178680GT87GENICheterozygous793822708
53317875833178759TC61GENICheterozygous793822709
53317964433179645AG39GENIChomozygous793822710
53318003433180035CT33GENIChomozygous793822711
53318044233180443CT39GENIChomozygous793822712
53318066033180661TC34GENIChomozygous793822713