chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263849527263849528GA20GENIChomozygous109217514
1263849931263849932GA22GENIChomozygous109217516
1263852685263852686AC20GENIChomozygous108634230
1263854925263854926GA22GENIChomozygous109217518
1263856252263856253GA19GENIChomozygous108634231
1263857028263857029GA14GENIChomozygous109217520
1263857120263857121CT8GENIChomozygous109217522
1263857996263857997CT27GENIChomozygous109217524
1263858010263858011TC24GENIChomozygous108634235
1263860023263860024CA18GENIChomozygous109217526
1263863064263863065TC21GENIChomozygous108634243
1263863424263863425GA25GENIChomozygous109217530
1263865531263865532AT19GENIChomozygous109217532
1263866911263866912CT23GENIChomozygous109217534
1263868167263868168AC18GENIChomozygous108634248
1263868212263868213GC16GENIChomozygous108634256
1263868804263868805GT8GENIChomozygous108634258
1263869043263869044AC20GENIChomozygous109217536
1263869995263869996CT16GENIChomozygous108634262
1263873064263873065TA30GENIChomozygous108634264
1263874361263874362TC12GENIChomozygous108634267
1263877375263877376GA7GENIChomozygous109217540
1263877639263877640TC19GENIChomozygous108634273
1263878839263878840AG20GENIChomozygous108634275
1263879592263879593GA22GENIChomozygous108634277
1263881256263881257AG26GENIChomozygous108634279
1263883303263883304TA27GENIChomozygous109217542
1263884191263884192GA11GENIChomozygous109217544