chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10736563	10736564	A	G	40	GENIC	homozygous	109634852
19	10736742	10736743	G	A	47	GENIC	homozygous	109634854
19	10737895	10737896	C	T	41	GENIC	homozygous	109634856
19	10738752	10738753	T	G	44	GENIC	homozygous	109634858
19	10738773	10738774	T	C	43	GENIC	homozygous	109634860
19	10739626	10739627	C	T	45	GENIC	homozygous	109634862
19	10739631	10739632	T	G	46	GENIC	homozygous	109634864
19	10739661	10739662	A	G	50	GENIC	homozygous	109634866
19	10739963	10739964	C	T	33	GENIC	homozygous	109634868
19	10740587	10740588	T	C	38	GENIC	homozygous	109634870
19	10740877	10740878	C	T	30	GENIC	homozygous	109634872
19	10742577	10742578	G	A	43	GENIC	homozygous	109634874
19	10742765	10742766	T	G	33	GENIC	homozygous	109634876
19	10744600	10744601	G	A	36	GENIC	homozygous	109634878
19	10746332	10746333	A	G	53	GENIC	homozygous	109634880
19	10747389	10747390	G	A	30	GENIC	homozygous	109634882
19	10748023	10748024	A	G	37	GENIC	homozygous	109634884
19	10749601	10749602	C	A	41	GENIC	possibly homozygous	109634886
19	10752571	10752572	G	A	42	GENIC	homozygous	109634888
19	10737908	10737912	TTTA		32	GENIC	homozygous	129583689
19	10748744	10748744		GA	9	GENIC	homozygous	129583690
19	10748779	10748779		GTGG	1	GENIC	homozygous	129583691
19	10748807	10748807		GTGGGTGGGTGT	1	GENIC	homozygous	129583692
19	10751516	10751516		TACTAGGTCCGTGGA	32	GENIC	homozygous	129583693
19	10748661	10748662	A	T	21	GENIC	homozygous	109764656