chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5170783627170783628AG11GENIChomozygous56089058
5170787571170787572CT8GENICpossibly homozygous56089062
5170788918170788919CT25GENICpossibly homozygous56089066
5170789083170789084GA23GENICpossibly homozygous56089067
5170790811170790812TC13GENICpossibly homozygous56089071
5170791119170791120CG16GENIChomozygous56089072
5170791770170791771TTG2GENIChomozygous55838751
5170791775170791776TTG2GENIChomozygous55838752
5170791779170791780TTG2GENIChomozygous55838753
5170791855170791856GGT1GENIChomozygous55838760
5170792043170792044GT1GENIChomozygous55838762
5170792045170792046AT1GENIChomozygous55838763
5170792047170792048GT1GENIChomozygous55838764
5170792676170792677CCT2GENICheterozygous56089076
5170792844170792845TG7GENIChomozygous56089077
5170792856170792857TG3GENIChomozygous56089078
5170792867170792868T-2GENIChomozygous55838766
5170793339170793340TC8GENICheterozygous56089080
5170793972170793973GA13GENIChomozygous56089081
5170797620170797621GA17GENICpossibly homozygous56089088
5170797879170797880T-2GENIChomozygous56089089
5170797993170797994AG7GENIChomozygous56089090
5170798073170798074GT11GENICheterozygous56089091
5170798180170798181AG7GENIChomozygous56089094
5170798189170798190TA8GENIChomozygous56089095
5170799684170799685AG13GENIChomozygous56089096
5170799981170799982TG2GENIChomozygous56089098
5170803831170803832CT11GENICpossibly homozygous56089104
5170804075170804076AT22GENICheterozygous56194425
5170804468170804469AG15GENICpossibly homozygous56194426
5170805745170805746TC16GENICpossibly homozygous56365137
5170792038170792039A-1GENIChomozygous56365135
5170793338170793339GT8GENICheterozygous56365136
5170807176170807177TA19GENIChomozygous56365138
5170807186170807187AG21GENIChomozygous56365139
5170807351170807352GT5GENIChomozygous55838778
5170807358170807359TTC3GENIChomozygous55838779
5170807940170807941GA9GENIChomozygous56194456
5170808054170808055AG7GENICheterozygous56089106