chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108955698889556989CT21GENIChomozygous664804585
108955804489558046TT--6GENICheterozygous766035327
108955814789558148GGTT7GENIChomozygous766035328
108955815689558157GT9GENIChomozygous664804586
108955848289558483CCTGTG27GENICpossibly homozygous766035329
108955891289558958ATATATATATATATATATATATATATATATATATATATACACACAC----------------------------------------------26GENICpossibly homozygous766035330
108955906189559062TA22GENIChomozygous664804587
108955921989559220AG20GENIChomozygous664804588
108955969189559692CA19GENIChomozygous664804589
108956009289560093GGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACA5GENICheterozygous766035331
108956012289560123CT5GENIChomozygous664804590
108956031289560313CT16GENIChomozygous664804591
108956072289560723GA32GENIChomozygous664804592
108956090289560903AG31GENIChomozygous664804593