chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43533476	43533477	G	A	17	GENIC	possibly homozygous	51435772
10	43535033	43535034	C	CT	18	GENIC	heterozygous	51435778
10	43535373	43535374	A	G	38	GENIC	homozygous	51435779
10	43536510	43536511	T	A	32	GENIC	possibly homozygous	51435780
10	43537189	43537190	T	C	22	GENIC	homozygous	52047474
10	43537313	43537314	A	G	27	GENIC	homozygous	51435781
10	43539488	43539489	G	GGAA	42	GENIC	homozygous	52147987
10	43539734	43539735	C	CTG	56	GENIC	homozygous	52147989
10	43540824	43540825	G	A	54	GENIC	homozygous	52147993
10	43541629	43541630	T	C	48	GENIC	homozygous	52147995
10	43541719	43541732	TAAAAAAAAAAAA	-------------	21	GENIC	homozygous	51435783
10	43541997	43541998	C	A	47	GENIC	homozygous	52147997
10	43542175	43542176	T	G	43	GENIC	homozygous	52147999
10	43542341	43542342	T	TG	23	GENIC	heterozygous	51435784
10	43543532	43543533	T	G	33	GENIC	heterozygous	51435786
10	43535219	43535220	T	TA	22	GENIC	heterozygous	52243983
10	43535337	43535338	T	G	43	GENIC	heterozygous	52243985
10	43540636	43540637	A	G	39	GENIC	homozygous	52243987
10	43540704	43540705	C	T	64	GENIC	possibly homozygous	52243989
10	43542341	43542342	T	TGG	23	GENIC	heterozygous	51435785
10	43543742	43543743	T	C	66	GENIC	homozygous	51435787