chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64373953743739538CT22GENIChomozygous114778380
64374213543742136AG22GENIChomozygous114778382
64374584643745847CG36GENICpossibly homozygous114778384
64374629043746291TC18GENIChomozygous114778386
64374791743747918AG26GENIChomozygous114778388
64374822343748224TG19GENIChomozygous114778390
64374824143748242TA15GENIChomozygous114778392
64374887443748875CT48GENIChomozygous114778394
64374897543748976GT38GENIChomozygous114778396
64374976243749763AG23GENIChomozygous114778398
64375041643750417TC41GENICpossibly homozygous114778400
64375119543751196TC36GENIChomozygous114778402
64375143943751440AT37GENIChomozygous114778404
64375444943754450AG32GENIChomozygous114778406
64376829643768297CG38GENIChomozygous118553153
64376829743768298GC38GENIChomozygous115057633
64376830643768307AG38GENIChomozygous114778408
64377460543774606TC32GENIChomozygous114778414
64377572043775721TC42GENIChomozygous114778418
64377576043775761GA37GENIChomozygous114778420
64377614443776145AG36GENIChomozygous114778422
64377676843776769TC19GENIChomozygous114778424
64377921843779219TC34GENIChomozygous114778426
64378018643780187CA21GENIChomozygous114778428
64378109743781098GA36GENIChomozygous114778430
64378701743787018GA32GENIChomozygous114778438
64378737043787371AG33GENIChomozygous114778440
64378808443788085CT39GENIChomozygous114778442
64378981643789817CG31GENIChomozygous114778444
64379242743792428CT29GENIChomozygous114778446
64379556943795570GA23GENIChomozygous114778448