chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199665283199665283CCCA52GENIChomozygous127472907
1199665328199665329AG54GENIChomozygous108501364
1199665459199665460TG60GENIChomozygous108501366
1199665825199665826AG70GENIChomozygous108501368
1199666088199666089TC55GENIChomozygous108501370
1199666108199666109GC54GENIChomozygous108501372
1199666141199666142T52GENIChomozygous127472908
1199666142199666143TC52GENIChomozygous120475414
1199666291199666292GA75GENIChomozygous108501374
1199666306199666307TC73GENIChomozygous108501376
1199666982199666983AG52GENIChomozygous108501378
1199667303199667303GAACTCA56GENIChomozygous127472909
1199667454199667455AG52GENICpossibly homozygous108501380
1199667470199667471TC57GENICpossibly homozygous108501382
1199667996199667997CT48GENIChomozygous108501384
1199668073199668074GA47GENIChomozygous108501386
1199668416199668417CT60GENIChomozygous108501388
1199668676199668676A58GENIChomozygous127472910
1199668765199668766CT61GENIChomozygous108501390
1199668816199668828AAGCAAACAAAC60GENIChomozygous127472911
1199668932199668933AG62GENIChomozygous108501392
1199669089199669090TC60GENIChomozygous108501394
1199669161199669162CA60GENIChomozygous108501396
1199669413199669414TC60GENIChomozygous108501398
1199670235199670236TC73GENIChomozygous108501400
1199670416199670417CT58GENIChomozygous108501402
1199670567199670567GGCCTACCCGAGTAGTGTAAG70GENIChomozygous127472912
1199670665199670666AT64GENIChomozygous108501404
1199670930199670931CG56GENIChomozygous108501406