chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10736563	10736564	A	G	26	GENIC	homozygous	109634852
19	10736742	10736743	G	A	10	GENIC	homozygous	109634854
19	10738752	10738753	T	G	29	GENIC	homozygous	109634858
19	10738773	10738774	T	C	26	GENIC	homozygous	109634860
19	10739626	10739627	C	T	23	GENIC	homozygous	109634862
19	10739631	10739632	T	G	23	GENIC	homozygous	109634864
19	10739661	10739662	A	G	21	GENIC	homozygous	109634866
19	10739963	10739964	C	T	7	GENIC	homozygous	109634868
19	10740587	10740588	T	C	19	GENIC	homozygous	109634870
19	10740877	10740878	C	T	23	GENIC	homozygous	109634872
19	10742577	10742578	G	A	17	GENIC	homozygous	109634874
19	10742765	10742766	T	G	34	GENIC	homozygous	109634876
19	10744600	10744601	G	A	23	GENIC	homozygous	109634878
19	10746332	10746333	A	G	24	GENIC	homozygous	109634880
19	10747389	10747390	G	A	17	GENIC	homozygous	109634882
19	10748023	10748024	A	G	26	GENIC	homozygous	109634884
19	10749601	10749602	C	A	17	GENIC	homozygous	109634886
19	10752571	10752572	G	A	12	GENIC	homozygous	109634888
19	10748661	10748662	A	T	12	GENIC	homozygous	109764656