chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
592347909234790T20GENIChomozygous130949913
592379389237938AC9GENIChomozygous130949914
592383779238378TG37GENICheterozygous119051035
592383789238379AT37GENICheterozygous113640771
592412989241299GT31GENIChomozygous114170569
592431209243120T18GENIChomozygous128149043
592436929243693GA21GENIChomozygous114170570
592441549244155A19GENICpossibly homozygous128149044
592443019244301CAATCTTTATCA20GENIChomozygous130949915
592448089244809G8GENIChomozygous130949916
592448219244825TTTA8GENICheterozygous130949917
592450099245010T18GENIChomozygous128149045
592450139245014TA18GENIChomozygous118941821
592457879245787T9GENICheterozygous130949918
592458139245814CT15GENIChomozygous114170571
592459319245932CT23GENIChomozygous114170572
592466539246655TG22GENICheterozygous131377557
592502469250247A20GENIChomozygous130949919
592512209251221T17GENIChomozygous128149046
592531339253133TT22GENIChomozygous130949920
592537889253789GA20GENIChomozygous113640779
592559989255999CG4GENIChomozygous114170573
592560099256010GT5GENIChomozygous113640781
592560129256013TC5GENIChomozygous113640783
592565129256512T19GENIChomozygous128149047