chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141873135318731354GA62GENIChomozygous113367616
141873136018731361T65GENIChomozygous129131089
141873166318731664AC18GENIChomozygous113367618
141873179218731793CT48GENIChomozygous113367620
141873190218731903CT53GENIChomozygous113367622
141873196318731965CT50GENIChomozygous129131090
141873196818731969GA50GENIChomozygous113367624
141873201518732016CT51GENIChomozygous113367626
141873207118732072CT51GENIChomozygous113367628
141873209618732097CT46GENIChomozygous113367630
141873211118732112AG42GENIChomozygous113367632
141873217718732178CA45GENIChomozygous113367634
141873225218732253CT52GENIChomozygous113367636
141873234818732349GC62GENIChomozygous113367638
141873238618732387TA63GENIChomozygous113367640
141873244718732448GA65GENIChomozygous113367642
141873246518732466AC62GENICpossibly homozygous113367644
141873250718732508TA53GENIChomozygous113367646
141873255418732555GA56GENIChomozygous113367648
141873269618732697AC80GENIChomozygous113367650
141873273018732731GA73GENIChomozygous113367652
141873281518732816GA61GENIChomozygous113367654
141873321818733219TC84GENIChomozygous113367656
141873338118733382TA56GENICpossibly homozygous113367658
141873235618732357T62GENIChomozygous129131091
141873242018732420A65GENIChomozygous129131092
141873251718732517CT55GENIChomozygous129131093