chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263849527263849528GA26GENIChomozygous109217514
1263849931263849932GA18GENIChomozygous109217516
1263852685263852686AC25GENIChomozygous108634230
1263854925263854926GA28GENIChomozygous109217518
1263856252263856253GA31GENIChomozygous108634231
1263857028263857029GA15GENIChomozygous109217520
1263857120263857121CT19GENIChomozygous109217522
1263857996263857997CT35GENIChomozygous109217524
1263858010263858011TC33GENIChomozygous108634235
1263860023263860024CA24GENIChomozygous109217526
1263863064263863065TC23GENICpossibly homozygous108634243
1263863424263863425GA27GENIChomozygous109217530
1263865531263865532AT21GENIChomozygous109217532
1263866911263866912CT23GENICpossibly homozygous109217534
1263868167263868168AC18GENIChomozygous108634248
1263868804263868805GT8GENIChomozygous108634258
1263868870263868871GA12GENIChomozygous120904989
1263869043263869044AC25GENIChomozygous109217536
1263869995263869996CT14GENIChomozygous108634262
1263873064263873065TA28GENIChomozygous108634264
1263874361263874362TC19GENIChomozygous108634267
1263877375263877376GA37GENIChomozygous109217540
1263877639263877640TC27GENIChomozygous108634273
1263878839263878840AG27GENICpossibly homozygous108634275
1263879592263879593GA18GENIChomozygous108634277
1263881256263881257AG33GENIChomozygous108634279
1263883303263883304TA31GENIChomozygous109217542