chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55804124858041249AG26GENIChomozygous114205895
55804317258043173TC23GENIChomozygous114205896
55804397958043980GT24GENIChomozygous113816734
55804418958044190TC28GENIChomozygous114205897
55804437058044371GT17GENIChomozygous114205898
55804449058044491TC16GENIChomozygous113816736
55804606358046064CT19GENIChomozygous114205899
55804624158046242TC15GENIChomozygous114205900
55804667258046673CT20GENIChomozygous114205901
55804724458047245CT21GENIChomozygous114205902
55804726558047266AG16GENIChomozygous114205903
55804763758047638GA17GENIChomozygous114205904
55805000458050005CT15GENIChomozygous114205905
55805117858051179AG23GENIChomozygous113816742
55805301958053020AC19GENIChomozygous114205906
55805375158053752CT23GENIChomozygous114205907
55805530558055306GA16GENIChomozygous114205908
55805690458056905AG24GENIChomozygous113816752
55805746458057465CA16GENIChomozygous113816754
55805816858058169CT19GENICheterozygous114205909
55805850458058505CT17GENIChomozygous114205910
55805951058059511AT19GENIChomozygous113816756
55806062158060622GA13GENIChomozygous113816760
55806438458064385CT29GENIChomozygous114205911
55807171658071717AG17GENIChomozygous113816772
55807274358072744CT20GENIChomozygous114205912
55807291158072912GA15GENIChomozygous114205913
55807339758073398GT16GENIChomozygous113816778
55807364658073647AG20GENIChomozygous113816780
55807495358074954GA19GENIChomozygous113816782
55807619658076197TC20GENIChomozygous113816788
55807652958076530CT25GENIChomozygous113816790
55807658158076582AG28GENIChomozygous113816792
55807675558076756CT7GENIChomozygous113816794
55807746158077462TG5GENIChomozygous113816798
55807754558077546CT16GENIChomozygous113816800
55807796958077970AT31GENICheterozygous114205914