chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57480092274800923AG10GENIChomozygous137508894
57480148874801489CT11GENIChomozygous137508895
57480174574801746GA16GENIChomozygous137508896
57480183174801832AT9GENIChomozygous137508897
57480209074802091CT8GENIChomozygous137508898
57480210374802104A9GENICpossibly homozygous403146241
57480210374802104AG9GENICheterozygous403146242
57480210774802108A9GENICpossibly homozygous403146243
57480210774802108AG9GENICheterozygous403146244
57480236674802367AC16GENIChomozygous137508899
57480249374802494CT21GENIChomozygous137508900
57480254774802548GA18GENIChomozygous137508901
57480279574802796TA16GENIChomozygous137508902
57480284374802844TC16GENIChomozygous137508903
57480342774803428CT15GENIChomozygous137508904
57480357274803573CT14GENIChomozygous137508905
57480361874803619CT12GENIChomozygous137508906
57480362874803629TC11GENIChomozygous137508907
57480374074803741CT10GENIChomozygous137508908
57480450074804501GC14GENIChomozygous137508909
57480510874805109CT15GENIChomozygous137508910
57480510974805110TC15GENIChomozygous137508911
57480546274805463CT10GENIChomozygous137508912
57480564974805650AC7GENIChomozygous137508913
57480571174805712TC10GENIChomozygous137508914
57480290474802904AAAC18GENICpossibly homozygous137317484
57480436574804365G15GENIChomozygous137317485
57480574674805746TAGTA8GENIChomozygous137317486
57480607074806071CT12GENIChomozygous137508915
57480749474807495GC16GENIChomozygous137508916
57480799274807993CA14GENIChomozygous137508917