chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109112820891128209TA19GENIChomozygous117088139
109112835291128353G10GENICheterozygous131902786
109112859791128598A12GENICheterozygous130394240
109112944891129449AG10GENIChomozygous117020662
109113023591130236GT15GENIChomozygous117088141
109113188291131883GA13GENIChomozygous117088143
109113234591132346TC18GENIChomozygous117088145
109113993191139932GA26GENIChomozygous117088151
109113439291134393AG26GENIChomozygous116905425
109113571691135717AG25GENIChomozygous116905431
109114030391140304AT24GENIChomozygous116905435
109114030491140305GA24GENIChomozygous116905437
109114123991141240TC12GENIChomozygous116905439
109114148591141486GC15GENIChomozygous118117212
109114192191141931CCCCACCCCA8GENIChomozygous131902787
109114211791142118GT21GENIChomozygous117088153
109114240191142402CT22GENIChomozygous117088155
109114292391142929TCCTCG12GENIChomozygous131902788
109114514691145147AG16GENIChomozygous117088157
109114600091146001GA15GENIChomozygous117088159
109114655491146555TC16GENIChomozygous116905441
109114673091146731CT23GENIChomozygous117088161
109114736291147363AG18GENIChomozygous116905443
109114806891148069CT19GENIChomozygous117088163
109114947091149471AG23GENIChomozygous116905445
109114955991149560AT24GENIChomozygous116905447
109114957991149580TC22GENIChomozygous116905449
109115073591150736TC24GENIChomozygous116905451
109115767991157681CG17GENIChomozygous131902789
109115948491159485GA22GENIChomozygous117105270
109115370791153708CT21GENIChomozygous117088165
109115411991154120TC36GENIChomozygous117088167
109115413391154134TC37GENIChomozygous117088169
109115863391158634TC18GENIChomozygous117088171
109115611291156113GC11GENIChomozygous118007841
109115980191159802GA15GENIChomozygous116905459
109116001091160011CT25GENIChomozygous116951768
109116031191160312AG20GENIChomozygous116905461