chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12400663624006636T27GENIChomozygous127366123
12400665224006653CT29GENIChomozygous120470930
12400665324006654TA30GENIChomozygous120470931
12400666224006663G26GENIChomozygous127366124
12401797824017978A10GENIChomozygous127366135
12402443524024436C10GENIChomozygous127366141
12402450724024508A14GENIChomozygous127366144
12402451524024516G14GENIChomozygous127366145
12402452724024528C16GENIChomozygous127366146
12402453524024535T17GENIChomozygous127366147
12402453824024539T17GENIChomozygous127366148
12402454124024542CA17GENIChomozygous108056224
12402454424024546AA19GENIChomozygous127366149
12402458024024580T20GENIChomozygous127366150
12402459624024597G19GENIChomozygous127366151
12402461324024614A24GENIChomozygous127366152
12402461824024619C23GENIChomozygous127366153
12402462724024628A23GENIChomozygous127366154
12402464724024648GT19GENIChomozygous108056225
12402469424024694GT17GENIChomozygous127366155
12402471824024719GT16GENIChomozygous108056226
12402473324024733G19GENIChomozygous127366157
12402473724024738G19GENIChomozygous127366158
12402451224024513AT14GENIChomozygous109409831
12402466124024662AC21GENIChomozygous120478690
12402466224024663TA21GENIChomozygous120552970