chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57480092274800923AG41GENIChomozygous137508894
57480148874801489CT40GENIChomozygous137508895
57480174574801746GA29GENIChomozygous137508896
57480183174801832AT19GENIChomozygous137508897
57480209074802091CT36GENIChomozygous137508898
57480210374802104A20GENICpossibly homozygous403146241
57480210374802104AG20GENICheterozygous403146242
57480210774802108A20GENICpossibly homozygous403146243
57480210774802108AG20GENICheterozygous403146244
57480236674802367AC35GENIChomozygous137508899
57480249374802494CT41GENIChomozygous137508900
57480254774802548GA45GENIChomozygous137508901
57480279574802796TA40GENIChomozygous137508902
57480284374802844TC39GENIChomozygous137508903
57480342774803428CT40GENIChomozygous137508904
57480357274803573CT48GENIChomozygous137508905
57480361874803619CT42GENIChomozygous137508906
57480362874803629TC44GENIChomozygous137508907
57480374074803741CT42GENIChomozygous137508908
57480450074804501GC45GENIChomozygous137508909
57480510874805109CT44GENIChomozygous137508910
57480510974805110TC44GENIChomozygous137508911
57480520274805203GC13GENIChomozygous403146245
57480520274805203G13GENICheterozygous403146246
57480520474805205GC13GENIChomozygous403146247
57480520674805207GC17GENICheterozygous140885828
57480524374805244A13GENIChomozygous403146248
57480524374805244AT13GENICheterozygous403146249
57480546274805463CT49GENIChomozygous137508912
57480564974805650AC40GENIChomozygous137508913
57480571174805712TC43GENIChomozygous137508914
57480607074806071CT48GENIChomozygous137508915
57480749474807495GC67GENIChomozygous137508916
57480799274807993CA81GENIChomozygous137508917
57480290474802904AAAC43GENIChomozygous137317484
57480436574804365G57GENIChomozygous137317485
57480574674805746TAGTA49GENIChomozygous137317486