chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104618280246182803AG37GENIChomozygous116877594
104618538346185384AG44GENICpossibly homozygous117410415
104618589246185893GA49GENIChomozygous116877596
104618698446186985CA51GENIChomozygous116877598
104618962646189627AG54GENIChomozygous116585224
104618469746184698CT33GENIChomozygous116585214
104618503546185036AG53GENIChomozygous116585218
104618457846184578T36GENIChomozygous128814161
104618848946188491CA52GENIChomozygous128814163
104618575046185751TC48GENIChomozygous116585220
104618741246187413CA49GENIChomozygous116585222
104619034446190345AT51GENIChomozygous116877600
104619051546190516TC66GENIChomozygous116585226
104619458146194582TC60GENICpossibly homozygous116585230
104619492246194923TG71GENIChomozygous116585232
104619529846195299GT52GENICpossibly homozygous116585234
104619623846196238AAAAC46GENIChomozygous128814166
104620004846200049A63GENIChomozygous128814171
104620087146200872TG53GENIChomozygous116877602
104620111346201114AG49GENIChomozygous116585236
104620127946201280GA52GENIChomozygous116877604
104620226346202266TTA18GENICheterozygous132145267
104620286146202861CAGGGCTA63GENIChomozygous128814172
104620301746203018AG70GENIChomozygous116877606
104618969346189703TATATGTGTA44GENIChomozygous131092518
104620373246203733TC55GENIChomozygous116585238
104620481346204814TG53GENIChomozygous116585240
104619564946195651AC48GENICheterozygous131092519