chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107514996475149965T62GENIChomozygous128831371
107515014775150148CG60GENIChomozygous116638399
107515043775150439AA58GENICpossibly homozygous128831372
107515044075150441A58GENICpossibly homozygous128831373
107515044375150443TG58GENICpossibly homozygous128831374
107515059275150595TTG27GENICpossibly homozygous128831375
107515060675150610TTTG27GENIChomozygous128831376
107515062875150628G29GENIChomozygous128831377
107515064075150641T27GENIChomozygous128831378
107515117575151176TG41GENIChomozygous116638401
107515242375152424CT53GENIChomozygous116638403
107515270375152704CG53GENIChomozygous116638405
107515356675153567AG52GENIChomozygous116638407
107515430675154307GA50GENIChomozygous116638409
107515519575155196GA52GENIChomozygous116638411
107515537175155372CG47GENIChomozygous116638413
107515542975155430TC48GENIChomozygous116638414
107515672775156727AAGG50GENIChomozygous128831379
107515848775158488GA65GENIChomozygous116638416
107515890875158912TATA54GENIChomozygous128831380
107515891675158917CG55GENIChomozygous116638418
107515899475158995TC62GENIChomozygous116638420
107515967475159675TC55GENIChomozygous116638422
107516046875160469AG55GENIChomozygous116638424
107515866375158664CT33GENIChomozygous117065589
107515586775155868GT41GENIChomozygous116800210
107515587775155878AT36GENIChomozygous116800212
107515602575156026A47GENICpossibly homozygous130682069
107515862575158626GA41GENIChomozygous117065587