chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121287705612877057AC19GENIChomozygous650190987
121287713912877140TTA19GENIChomozygous757229457
121287720212877203TC25GENIChomozygous650190988
121287748312877484AG17GENICheterozygous650190989
121287774912877750TA10GENIChomozygous650190990
121287861312878614AC20GENICpossibly homozygous650190991
121287907012879073AAT---12GENIChomozygous757229458
121288253212882533TA10GENICheterozygous650190992
121288318712883188TTCATACATACATA7GENIChomozygous757229459
121288381312883814C-28GENICheterozygous757229460
121288384812883896GGGCATGAGGAGAAAATCATAGGTCATGTCAGGAGGGACCATCACAGA------------------------------------------------43GENICheterozygous757229461
121288394212883945TGG---23GENICheterozygous757229462
121288514512885146CG31GENIChomozygous650190993
121288517712885178CA37GENICheterozygous650190994
121288523412885235AG22GENICheterozygous650190995
121288524012885241TA21GENICheterozygous650190996
121288524212885243CT21GENICheterozygous650190997
121288527612885278AT--19GENICheterozygous757229463
121288528312885284TTGC20GENICheterozygous757229464
121288532012885321AAT30GENICheterozygous757229465
121288533612885337GGT28GENICheterozygous757229466
121288535812885361GGG---24GENICheterozygous757229467
121288536112885362GGAT23GENICheterozygous757229468
121288548812885489CA39GENICheterozygous650190998
121288549212885493GA40GENICheterozygous650190999
121288579912885817CTTTATGTTAAGAGCAAA------------------34GENICheterozygous757229469
121288602712886028TTG33GENICheterozygous757229473
121288611812886119AG29GENIChomozygous650191000
121288616012886161AAG30GENICheterozygous757229474
121288624212886243GGTA33GENICheterozygous757229475
121288624312886244GA34GENICheterozygous650191001
121288639212886393A-28GENICheterozygous757229476