chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182470913824709139AG13GENIChomozygous110309042
182471123124711232GA10GENIChomozygous110309044
182471235324712354TA20GENIChomozygous110309046
182471520424715205GA16GENICpossibly homozygous110309057
182471569824715699TC34GENIChomozygous110309059
182471603824716039CA29GENIChomozygous110309061
182471891424718915GT18GENIChomozygous110309063
182472100024721001AG30GENIChomozygous110309065
182472246624722467AG31GENIChomozygous110309067
182472905424729055AG52GENICpossibly homozygous110309069
182473044524730446CT28GENIChomozygous110309071
182473241424732415TC23GENIChomozygous110309073
182473264624732647AG19GENIChomozygous110309075
182473281924732820AG17GENIChomozygous110309077
182473299524732996GA31GENIChomozygous110309079
182473520324735204GA21GENIChomozygous110309085
182473328624733287GA29GENIChomozygous110309081
182473361724733618GA24GENIChomozygous110309083
182473587024735871AG24GENIChomozygous110309087
182473616724736168CT25GENIChomozygous110309089
182473668724736688TC21GENIChomozygous110309091
182474030224740303AT33GENIChomozygous110309093
182474129524741296CT27GENIChomozygous110309095
182474296424742965TA23GENIChomozygous110309097
182474485124744852CT26GENIChomozygous110309099
182474493524744936CT31GENIChomozygous110309101
182474553424745535CT19GENIChomozygous110309103