chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55949076359490764AG20GENIChomozygous954983103
55949103459491035GA30GENIChomozygous954983104
55949108759491088AC18GENICheterozygous954983105
55949225259492253GA29GENIChomozygous954983106
55949242559492426AG19GENIChomozygous954983107
55949329359493294TC26GENIChomozygous954983108
55949334459493345CT37GENIChomozygous954983109
55949402159494022GT31GENIChomozygous954983110
55949502159495022AG26GENIChomozygous954983111
55949624259496243AG32GENIChomozygous954983112
55949727059497271GA34GENIChomozygous954983113
55950017959500180AG30GENIChomozygous954983114
55950082859500829GC29GENIChomozygous954983115
55950087359500874GA41GENIChomozygous954983116
55950087559500876CT40GENIChomozygous954983117
55950220759502208CA31GENIChomozygous954983118
55950224359502244CT28GENIChomozygous954983119
55950230059502301GA30GENIChomozygous954983120
55950234059502341CT31GENIChomozygous954983121
55950246859502469CT35GENIChomozygous954983122
55950268359502684TC31GENIChomozygous954983123
55950323259503233CT32GENIChomozygous954983124
55950324559503246CT38GENIChomozygous954983125
55950345359503454CT37GENIChomozygous954983126
55950351459503515TC32GENIChomozygous954983127
55950372059503721TC31GENIChomozygous954983128
55950411659504117TC19GENIChomozygous954983129
55950448859504489AG24GENIChomozygous954983130
55950488859504889TC32GENIChomozygous954983131
55950514059505141CT29GENIChomozygous954983132
55950546359505464TC27GENIChomozygous954983133
55950571859505719GA30GENIChomozygous954983134