chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81336581813365819CT31GENIChomozygous116924120
81336601113366012CT34GENIChomozygous116924121
81336634513366346TC26GENIChomozygous116924123
81336847913368480TC30GENIChomozygous116924125
81336849213368493GA36GENIChomozygous116924127
81337043813370439GA36GENIChomozygous116924129
81337064813370649CT27GENIChomozygous116924131
81337100813371009AG20GENIChomozygous116924133
81337162113371622TG21GENIChomozygous116924135
81337162513371626TC22GENIChomozygous116924136
81337180713371808GA36GENIChomozygous116924138
81337230913372310TC22GENIChomozygous116924140
81337282513372826GC24GENIChomozygous116924142
81337307413373075GA28GENIChomozygous116924144
81337347513373476TC27GENIChomozygous116924146
81337375113373752CT29GENIChomozygous116924147
81337446913374470CT22GENIChomozygous116924149
81337512513375126TA23GENIChomozygous116924151
81337517713375178TA18GENIChomozygous116924153
81337526213375263TC27GENIChomozygous116924155