chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161909741119097412GA43GENIChomozygous971024245
161909779819097799CT34GENIChomozygous971024246
161909817519098176GT29GENIChomozygous971024247
161909930319099304TA50GENIChomozygous971024248
161909955919099560AG19GENIChomozygous971024249
161909976019099761AG31GENIChomozygous971024250
161909977219099773TC34GENIChomozygous971024251
161909983319099834TC54GENIChomozygous971024252
161909990219099903GA51GENIChomozygous971024253
161910008019100081CT29GENIChomozygous971024254
161910008119100082AG29GENIChomozygous971024255
161910045619100457CT29GENIChomozygous971024256
161910090719100908TG22GENIChomozygous971024257
161910156819101569GA29GENIChomozygous971024258
161910184519101846TC40GENIChomozygous971024259
161910255019102551TG35GENIChomozygous971024260
161910344019103441CA22GENIChomozygous971024261
161910530319105304TC23GENIChomozygous971024262
161911392519113926CT21GENIChomozygous971024263
161911547419115475TC30GENIChomozygous971024264
161911558019115581GA18GENIChomozygous971024265
161911899219118993CT26GENIChomozygous971024266
161911913719119138GA46GENIChomozygous971024267
161912265619122657TA45GENIChomozygous971024268
161912367519123676AC39GENIChomozygous971024269