chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1637556903755691CT47GENIChomozygous112197683
1637558443755845GA50GENIChomozygous112197685
1637560603756061TC49GENIChomozygous112197687
1637562743756275CT50GENIChomozygous112197689
1637563743756375GT44GENIChomozygous112197691
1637568683756869T50GENIChomozygous133029156
1637569433756944CT47GENIChomozygous112197693
1637572973757298CT47GENIChomozygous112197695
1637575493757550GT55GENIChomozygous112197697
1637582443758245GA31GENIChomozygous112197699
1637589343758934GCCAGAGACAGAGAGCAAGC39GENIChomozygous133029157
1637601693760172TTG24GENIChomozygous133029158
1637584803758481CT48GENIChomozygous112197701
1637585423758543CT46GENIChomozygous112197703
1637586423758643CT50GENIChomozygous112197705
1637589073758908GA43GENIChomozygous112197707
1637603933760394AC54GENIChomozygous112197709
1637607133760714GA48GENIChomozygous112197711
1637607433760744CT46GENIChomozygous112197713
1637609643760965AG48GENIChomozygous112197715
1637610123761012A50GENIChomozygous133029159
1637610143761015TA50GENIChomozygous112197717
1637612093761210CA23GENIChomozygous112197719
1637614703761471GA16GENICpossibly homozygous112197721
1637616733761674GA59GENIChomozygous112197723
1637623143762315TC48GENIChomozygous112197725
1637623493762350TC54GENIChomozygous112197727
1637630323763033A46GENIChomozygous133029160
1637630383763039CT48GENIChomozygous112197729
1637631633763178CCCTCTCCCTCTCCC25GENIChomozygous133029161
1637638973763905CCAAGAAG42GENIChomozygous133029162
1637640203764021AG47GENIChomozygous112197731
1637642943764295GA52GENIChomozygous111702014
1637649443764945TA50GENIChomozygous111702016
1637651063765107GC48GENIChomozygous112197733
1637653293765330TA33GENIChomozygous112197735
1637653383765339AT33GENIChomozygous112197737
1637654553765456CT36GENIChomozygous112197739
1637609623760963A48GENIChomozygous129327859
1637631413763142CA28GENICpossibly homozygous133031377
1637631503763151TA28GENIChomozygous133031378
1637632283763229CT21GENIChomozygous133031379