chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108955698889556989CT28GENICpossibly homozygous653822790
108955804489558046TT--10GENICheterozygous759355070
108955814789558148GGTT7GENIChomozygous759355071
108955815689558157GT8GENIChomozygous653822791
108955848289558483CCTGTG23GENIChomozygous759355072
108955891289558958ATATATATATATATATATATATATATATATATATATATACACACAC----------------------------------------------18GENICpossibly homozygous759355073
108955906189559062TA23GENIChomozygous653822792
108955921989559220AG25GENIChomozygous653822793
108955969189559692CA29GENIChomozygous653822794
108956009289560093GGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACA19GENICheterozygous759355074
108956012289560123CT20GENIChomozygous653822795
108956031289560313CT25GENICpossibly homozygous653822796
108956072289560723GA29GENIChomozygous653822797
108956090289560903AG31GENIChomozygous653822798