chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143455563234555633TC50GENIChomozygous113419762
143455567634555677CT55GENIChomozygous113419763
143455575334555754CT65GENIChomozygous113419764
143455592934555930AC42GENIChomozygous113419765
143455646634556467AT38GENIChomozygous113419766
143455708034557081CT49GENIChomozygous113419767
143455778034557781TC19GENIChomozygous113419768
143455814834558149GA38GENIChomozygous113419769
143455828134558282TC46GENIChomozygous113419770
143455858934558590CT47GENIChomozygous113419771
143455912534559126GA57GENIChomozygous113419772
143455925734559258TG51GENIChomozygous113419773
143455989034559891CT46GENIChomozygous113419774
143455989134559892TG45GENIChomozygous113419775
143456224934562250GA36GENIChomozygous113419776
143456233234562333AG32GENIChomozygous113419777
143455792434557924T30GENIChomozygous129144859
143455984034559840ACAGCC52GENIChomozygous129144860
143456595134565955TTCT25GENIChomozygous129144861
143456692434566924AC44GENIChomozygous129144862
143456775734567758GA48GENIChomozygous113419778
143456854734568548TC57GENIChomozygous113419779
143456880334568804CG48GENIChomozygous113419780
143456911134569112AG52GENIChomozygous113419781
143457041734570418CT54GENICpossibly homozygous113419782
143456966834569668GC10GENICheterozygous132724089