chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X10376601037661TG9GENIChomozygous108437026
X10423231042324AG10GENICheterozygous125127607
X10423571042358CA5GENICheterozygous125097932
X10430541043055TA11GENICheterozygous108437029
X10440951044096GT3GENICheterozygous108215745
X10442701044271GT6GENICheterozygous108215748
X10444271044428TA7GENICheterozygous125147479
X10449531044954GA4GENICheterozygous125147480
X10452311045232AC5GENIChomozygous125147481
X10473781047379CT13GENICheterozygous125127608
X10473961047397CT9GENICheterozygous125127609
X10548621054863AT7GENICheterozygous125097933
X10554801055481GT6GENIChomozygous108215765
X10574341057435AC11GENIChomozygous108681932
X10585131058514AT4GENICheterozygous120782913
X10585141058515TA4GENICheterozygous125147482
X10596271059628TG3GENICheterozygous125147483
X10604951060496GC4GENICheterozygous125097936
X10608251060826TC7GENIChomozygous108215773
X10617111061712AC3GENICheterozygous125147484
X10624711062472CT14GENIChomozygous108215778
X10640321064033TC11GENIChomozygous108215781
X10644991064500TA6GENICheterozygous125097938
X10717081071709CT13GENIChomozygous108215788
X10724641072465GT6GENIChomozygous108215790
X10729431072944TG13GENIChomozygous108215793
X10729841072985GA4GENIChomozygous108437035
X10753391075340GA7GENIChomozygous108437039
X10793011079302TA4GENIChomozygous125147485
X10824511082452AT5GENICheterozygous125147486
X10912981091299GA7GENIChomozygous108215795
X10918821091883CA14GENIChomozygous108215798
X10923561092357AG4GENIChomozygous108215801
X10945551094556AG9GENIChomozygous108215806
X10963401096341GA13GENICheterozygous108630385
X10989761098977GA36GENICheterozygous125097941
X10989971098998TA46GENICheterozygous125097942
X10990211099022TA16GENICheterozygous125097943
X11016791101680AC12GENIChomozygous108215809
X11040871104088GA10GENIChomozygous108215811
X11069061106907TC11GENIChomozygous108215814
X11097441109745AC9GENIChomozygous108215816
X11097531109754AC6GENIChomozygous108215818