chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199665283199665283CCCA6GENIChomozygous127472907
1199665328199665329AG8GENIChomozygous108501364
1199665459199665460TG16GENIChomozygous108501366
1199666141199666142T21GENIChomozygous127472908
1199666142199666143TC21GENIChomozygous120475414
1199665825199665826AG12GENIChomozygous108501368
1199666088199666089TC17GENIChomozygous108501370
1199666108199666109GC14GENIChomozygous108501372
1199666291199666292GA18GENIChomozygous108501374
1199666306199666307TC18GENIChomozygous108501376
1199666982199666983AG17GENIChomozygous108501378
1199667303199667303GAACTCA21GENIChomozygous127472909
1199667454199667455AG17GENIChomozygous108501380
1199667470199667471TC17GENIChomozygous108501382
1199667996199667997CT14GENIChomozygous108501384
1199668073199668074GA15GENIChomozygous108501386
1199668416199668417CT20GENIChomozygous108501388
1199668676199668676A20GENIChomozygous127472910
1199668765199668766CT22GENIChomozygous108501390
1199668816199668828AAGCAAACAAAC21GENIChomozygous127472911
1199668932199668933AG26GENIChomozygous108501392
1199669089199669090TC16GENIChomozygous108501394
1199669161199669162CA22GENIChomozygous108501396
1199669413199669414TC18GENIChomozygous108501398
1199670235199670236TC30GENIChomozygous108501400
1199670416199670417CT18GENIChomozygous108501402
1199670567199670567GGCCTACCCGAGTAGTGTAAG18GENIChomozygous127472912
1199670665199670666AT16GENIChomozygous108501404
1199670930199670931CG11GENIChomozygous108501406