chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140845519140845520A17GENIChomozygous128085276
4140855546140855547A14GENIChomozygous129904458
4140855588140855589G13GENIChomozygous129904460
4140855591140855591A13GENIChomozygous129904461
4140855596140855596T13GENIChomozygous129904462
4140855619140855619G8GENIChomozygous129904463
4140855638140855639A7GENIChomozygous129904464
4140855646140855646A5GENIChomozygous129904465
4140855648140855649A5GENIChomozygous129904466
4140855669140855670CA5GENIChomozygous112858130
4140855674140855677CTA5GENIChomozygous129904467
4140855720140855721CA12GENIChomozygous112858132
4140855741140855741A8GENIChomozygous128085279
4140855755140855756T6GENIChomozygous128085280
4140855762140855762G6GENIChomozygous128085281
4140855764140855764C6GENIChomozygous128085282
4140855785140855785A5GENIChomozygous128085283
4140855787140855788AT4GENIChomozygous122131880
4140855790140855791AT4GENIChomozygous122131881
4140855791140855792CA4GENIChomozygous122131882
4140855795140855795A4GENIChomozygous128085284
4140855805140855806G3GENIChomozygous128085285
4140855808140855809C3GENIChomozygous128085286
4140855811140855813CT3GENIChomozygous128085287
4140855800140855801AT3GENIChomozygous119477011
4140857065140857066CT28GENICheterozygous129910688
4140857086140857087CT26GENICheterozygous113471138
4140857100140857101TC29GENICheterozygous113057505
4140857115140857116CT25GENICheterozygous112858142
4140857132140857133TA28GENICheterozygous112858144
4140857139140857140T26GENICheterozygous129904468
4140857155140857156GT29GENICheterozygous112858146
4140857160140857160TATT31GENICheterozygous129904469
4140857183140857184AT29GENICheterozygous113307136
4140857188140857189TC29GENICheterozygous113307137
4140857191140857193TT29GENICheterozygous129904470
4140863675140863675AC23GENIChomozygous128085290
4140864721140864721A17GENIChomozygous128085291
4140875612140875613CA27GENICheterozygous130549743
4140875628140875629GC29GENICheterozygous130549744