chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111423384111423385CT24GENIChomozygous949467131
3111425983111425984GC12GENIChomozygous949467132
3111427053111427054GC22GENIChomozygous949467133
3111428965111428966AG10GENIChomozygous949467134
3111429442111429443TC6GENIChomozygous949467135
3111429609111429610AC9GENIChomozygous949467136
3111430237111430238GA12GENIChomozygous949467137
3111431398111431399GA20GENIChomozygous949467138
3111432156111432157GA15GENIChomozygous949467139
3111432680111432681GA19GENIChomozygous949467140
3111434551111434552CA17GENICpossibly homozygous949467141
3111436304111436305AG19GENIChomozygous949467142
3111437233111437234TG17GENIChomozygous949467143
3111439159111439160CT15GENIChomozygous949467144
3111439677111439678CT17GENIChomozygous949467145
3111440006111440007AG3GENIChomozygous949467146
3111441752111441753CT21GENIChomozygous949467147
3111442247111442248TC23GENIChomozygous949467148
3111444789111444790CT24GENIChomozygous949467149
3111445266111445267AG23GENIChomozygous949467150
3111445739111445740GA19GENIChomozygous949467151
3111446036111446037TC15GENIChomozygous949467152
3111446091111446092TG24GENIChomozygous949467153
3111446383111446384TC11GENIChomozygous949467154
3111446447111446448TC23GENIChomozygous949467155
3111446875111446876AT12GENIChomozygous949467156
3111451135111451136TC17GENIChomozygous949467157