chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54151344	54151345	G	A	58	GENIC	homozygous	109732908
19	54152259	54152260	T	G	55	GENIC	homozygous	109732910
19	54155704	54155705	A	G	50	GENIC	homozygous	109732912
19	54156044	54156045	T	C	65	GENIC	homozygous	109732914
19	54156720	54156721	G	A	70	GENIC	homozygous	109732916
19	54156735	54156736	C	T	66	GENIC	homozygous	109732919
19	54157813	54157814	C	T	47	GENIC	homozygous	109732921
19	54158418	54158419	A	G	77	GENIC	homozygous	109732923
19	54158538	54158539	G	A	83	GENIC	possibly homozygous	109732925
19	54159390	54159391	C	T	74	GENIC	homozygous	109732927
19	54160283	54160284	C	T	57	GENIC	homozygous	109732929
19	54160987	54160988	T	C	39	GENIC	homozygous	109875779
19	54163253	54163254	G	A	54	GENIC	homozygous	109732933
19	54163483	54163484	C	A	43	GENIC	homozygous	109732935
19	54154037	54154038	G	A	58	GENIC	homozygous	119633211
19	54157344	54157345	A	G	24	GENIC	homozygous	119633212
19	54160527	54160544	AAAAAAAAGAACCAAAA		21	GENIC	heterozygous	132365234
19	54160557	54160558	A	G	17	GENIC	heterozygous	132367446