chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171698171216981713AAT4GENIChomozygous757604144
171698180316981804AT6GENIChomozygous650850919
171698183916981840TA11GENICpossibly homozygous650850920
171698184716981848GA11GENIChomozygous650850921
171698186616981867CT5GENIChomozygous650850922
171698192716981928CT5GENICheterozygous650850923
171698192916981930CT5GENICheterozygous650850924
171698193116981932TTG5GENIChomozygous757604145
171698239116982393TG--15GENICpossibly homozygous757604146
171698329216983293T-16GENICheterozygous757604147
171698331116983312GA19GENIChomozygous650850925
171698348816983489TTTTC21GENICheterozygous757604148
171698362516983641TTTATTTATTTATTTA----------------17GENIChomozygous757604149
171698455916984560C-27GENICheterozygous757604150
171698461116984612GT27GENIChomozygous650850926
171698463016984631TG28GENIChomozygous650850927
171698486516984866AAGGG16GENIChomozygous757604151
171698487116984872T-20GENICheterozygous757604152
171698508116985082GGT34GENICheterozygous757604153
171698562916985630CCT37GENICheterozygous757604154
171698569416985695TA31GENIChomozygous650850928
171698579616985797TC47GENIChomozygous650850929
171698594816985949GGGAATGTTGA24GENICheterozygous757604155
171698595116985952C-25GENICheterozygous757604156
171698595316985954GGACAGTATATTTACTAAAGGGTCATGGAAAT21GENICheterozygous757604157
171698598916985990CG7GENIChomozygous650850930
171698599016985991TG7GENIChomozygous650850931
171698605016986057TTTCCTC-------13GENIChomozygous757604158
171698630516986306TG20GENIChomozygous650850932
171699243516992436TC10GENIChomozygous650850933
171699255316992554CT6GENIChomozygous650850934
171699258616992587TA7GENIChomozygous650850935
171699264216992643TG14GENIChomozygous650850936
171699288016992881AG18GENIChomozygous650850937
171699293516992936AT14GENIChomozygous650850938
171699345116993452TTG19GENICheterozygous757604159
171699365716993658TTA29GENICheterozygous757604160
171699457316994574AC11GENIChomozygous650850939
171699537916995380GC13GENIChomozygous650850940