chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67773535877735359CT7GENIChomozygous114865086
67773552777735528TC15GENIChomozygous114865087
67773577177735772GT21GENIChomozygous115260344
67773632577736326CT17GENIChomozygous114865090
67773651577736516TC20GENIChomozygous114865091
67773696977736970TC19GENIChomozygous115260346
67773729777737298TC11GENIChomozygous114865093
67773731977737320TC8GENIChomozygous114865094
67773783777737838CT31GENIChomozygous115260348
67773811177738112TG27GENIChomozygous114865096
67773921877739219AC17GENIChomozygous115260350
67773982677739827CT20GENIChomozygous115260352
67774079077740791AC20GENIChomozygous115260354
67774092377740924TC20GENIChomozygous115260356
67774130877741309CT11GENIChomozygous114865102
67774217577742176GA16GENIChomozygous114865108
67774229477742295AC5GENIChomozygous118574273
67774280977742810TG17GENIChomozygous115260360
67774301977743020CT16GENIChomozygous115260362
67774372277743723CT17GENIChomozygous115260364
67774421477744215CT16GENIChomozygous114865112
67774474977744750CT16GENIChomozygous115260366
67774529677745297TA32GENIChomozygous115260368
67774562277745623AG16GENIChomozygous115260370
67774623177746232AT16GENIChomozygous115260372
67774746277747463TC20GENIChomozygous115260374
67774862377748624GA25GENICpossibly homozygous114865121
67774953977749540GA14GENIChomozygous115260376
67774956077749561GA14GENIChomozygous115260378
67774972077749721AG20GENICpossibly homozygous114865122
67774996877749969CT19GENIChomozygous115260382
67775102677751027AC12GENIChomozygous115260384