chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199665283199665283CCCA23GENIChomozygous127472907
1199665328199665329AG29GENIChomozygous108501364
1199665459199665460TG25GENIChomozygous108501366
1199665825199665826AG24GENIChomozygous108501368
1199666088199666089TC20GENIChomozygous108501370
1199666108199666109GC21GENIChomozygous108501372
1199666141199666142T22GENIChomozygous127472908
1199666142199666143TC22GENIChomozygous120475414
1199666291199666292GA27GENIChomozygous108501374
1199666306199666307TC25GENIChomozygous108501376
1199666982199666983AG21GENIChomozygous108501378
1199667303199667303GAACTCA30GENIChomozygous127472909
1199667454199667455AG25GENIChomozygous108501380
1199667470199667471TC21GENIChomozygous108501382
1199667996199667997CT22GENIChomozygous108501384
1199668073199668074GA16GENIChomozygous108501386
1199668416199668417CT25GENIChomozygous108501388
1199668676199668676A24GENIChomozygous127472910
1199668765199668766CT17GENIChomozygous108501390
1199668816199668828AAGCAAACAAAC19GENIChomozygous127472911
1199668932199668933AG18GENIChomozygous108501392
1199669089199669090TC21GENIChomozygous108501394
1199669161199669162CA18GENIChomozygous108501396
1199669413199669414TC18GENIChomozygous108501398
1199670235199670236TC29GENIChomozygous108501400
1199670416199670417CT19GENIChomozygous108501402
1199670567199670567GGCCTACCCGAGTAGTGTAAG12GENIChomozygous127472912
1199670665199670666AT17GENICpossibly homozygous108501404
1199670930199670931CG16GENIChomozygous108501406