chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	50111996	50111997	C	T	43	GENIC	homozygous	47672581
16	50112006	50112007	T	C	44	GENIC	homozygous	47672582
16	50112187	50112189	AA	--	62	GENIC	homozygous	47672583
16	50112437	50112438	A	G	78	GENIC	homozygous	47444633
16	50113809	50113810	C	A	66	GENIC	homozygous	47672584
16	50114684	50114685	C	T	65	GENIC	homozygous	47672585
16	50119989	50119990	T	C	50	GENIC	homozygous	47444649
16	50122688	50122689	G	A	64	GENIC	possibly homozygous	47444651
16	50125528	50125529	C	T	57	GENIC	possibly homozygous	47672586
16	50125552	50125553	A	-	51	GENIC	homozygous	47444665
16	50125797	50125798	C	A	80	GENIC	homozygous	47672587
16	50126038	50126039	G	A	50	GENIC	possibly homozygous	47672588
16	50127275	50127276	T	C	47	GENIC	homozygous	47444670
16	50128473	50128474	G	T	58	GENIC	homozygous	47444678
16	50128557	50128558	C	T	67	GENIC	possibly homozygous	47672589
16	50128760	50128761	C	CCATGTGGA	24	GENIC	homozygous	47444680
16	50129862	50129863	T	C	75	GENIC	possibly homozygous	47444685
16	50130726	50130727	C	T	59	GENIC	homozygous	47444689
16	50130985	50130986	T	C	54	GENIC	homozygous	47444691
16	50132329	50132330	C	T	70	GENIC	homozygous	47672590
16	50133083	50133084	A	C	69	GENIC	homozygous	47444693
16	50133216	50133217	T	C	72	GENIC	homozygous	47672591
16	50133330	50133331	T	TGA	24	GENIC	heterozygous	47444695
16	50133332	50133333	A	T	38	GENIC	heterozygous	47444697
16	50133348	50133350	AA	--	33	GENIC	possibly homozygous	47444699
16	50133355	50133356	G	C	38	GENIC	heterozygous	47672592
16	50133367	50133368	G	C	33	GENIC	heterozygous	47672593
16	50133377	50133378	C	G	29	GENIC	homozygous	47444703
16	50133749	50133750	C	T	67	GENIC	homozygous	47672594
16	50134101	50134102	C	T	50	GENIC	homozygous	47672595
16	50134583	50134584	A	G	61	GENIC	homozygous	47444705
16	50135094	50135095	A	G	58	GENIC	homozygous	47444707
16	50135907	50135908	A	G	68	GENIC	homozygous	47444711
16	50136149	50136150	G	A	57	GENIC	homozygous	47444713
16	50136435	50136436	C	CT	29	GENIC	homozygous	47672596