chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108955698889556989CT32GENIChomozygous573534176
108955804489558046TT--8GENICheterozygous712995016
108955814789558148GGTT7GENIChomozygous712995017
108955815689558157GT6GENIChomozygous573534177
108955848289558483CCTGTG25GENICpossibly homozygous712995018
108955891289558958ATATATATATATATATATATATATATATATATATATATACACACAC----------------------------------------------20GENICpossibly homozygous712995019
108955906189559062TA20GENIChomozygous573534178
108955921989559220AG26GENIChomozygous573534179
108955969189559692CA19GENIChomozygous573534180
108956009289560093GGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACA6GENICheterozygous712995020
108956012289560123CT13GENIChomozygous573534181
108956031289560313CT35GENIChomozygous573534182
108956072289560723GA41GENIChomozygous573534183
108956090289560903AG32GENIChomozygous573534184