chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57480092274800923AG48GENIChomozygous137508894
57480148874801489CT36GENIChomozygous137508895
57480174574801746GA28GENIChomozygous137508896
57480183174801832AT28GENIChomozygous137508897
57480209074802091CT28GENIChomozygous137508898
57480210774802108AG20GENICheterozygous403146244
57480210374802104A20GENICpossibly homozygous403146241
57480210374802104AG20GENICheterozygous403146242
57480210774802108A20GENICpossibly homozygous403146243
57480236674802367AC39GENIChomozygous137508899
57480249374802494CT49GENIChomozygous137508900
57480254774802548GA40GENIChomozygous137508901
57480279574802796TA49GENIChomozygous137508902
57480284374802844TC49GENIChomozygous137508903
57480342774803428CT46GENIChomozygous137508904
57480357274803573CT43GENIChomozygous137508905
57480361874803619CT33GENIChomozygous137508906
57480362874803629TC35GENIChomozygous137508907
57480374074803741CT34GENIChomozygous137508908
57480450074804501GC56GENIChomozygous137508909
57480510874805109CT43GENIChomozygous137508910
57480510974805110TC43GENIChomozygous137508911
57480546274805463CT40GENIChomozygous137508912
57480564974805650AC47GENIChomozygous137508913
57480571174805712TC38GENIChomozygous137508914
57480607074806071CT40GENIChomozygous137508915
57480749474807495GC59GENIChomozygous137508916
57480799274807993CA43GENIChomozygous137508917
57480290474802904AAAC43GENIChomozygous137317484
57480436574804365G43GENIChomozygous137317485
57480574674805746TAGTA36GENIChomozygous137317486