chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	50111996	50111997	C	T	14	GENIC	homozygous	47672581
16	50112006	50112007	T	C	15	GENIC	possibly homozygous	47672582
16	50112187	50112189	AA	--	20	GENIC	homozygous	47672583
16	50112437	50112438	A	G	21	GENIC	homozygous	47444633
16	50113809	50113810	C	A	13	GENIC	homozygous	47672584
16	50114684	50114685	C	T	17	GENIC	homozygous	47672585
16	50119989	50119990	T	C	33	GENIC	homozygous	47444649
16	50122688	50122689	G	A	13	GENIC	homozygous	47444651
16	50125528	50125529	C	T	16	GENIC	homozygous	47672586
16	50125552	50125553	A	-	16	GENIC	homozygous	47444665
16	50125797	50125798	C	A	26	GENIC	homozygous	47672587
16	50126038	50126039	G	A	27	GENIC	possibly homozygous	47672588
16	50127275	50127276	T	C	35	GENIC	homozygous	47444670
16	50128473	50128474	G	T	22	GENIC	homozygous	47444678
16	50128557	50128558	C	T	18	GENIC	homozygous	47672589
16	50128760	50128761	C	CCATGTGGA	15	GENIC	homozygous	47444680
16	50129862	50129863	T	C	36	GENIC	homozygous	47444685
16	50130726	50130727	C	T	29	GENIC	homozygous	47444689
16	50130985	50130986	T	C	26	GENIC	homozygous	47444691
16	50132329	50132330	C	T	28	GENIC	homozygous	47672590
16	50133083	50133084	A	C	23	GENIC	homozygous	47444693
16	50133216	50133217	T	C	28	GENIC	homozygous	47672591
16	50133330	50133331	T	TGA	8	GENIC	possibly homozygous	47444695
16	50133332	50133333	A	T	14	GENIC	possibly homozygous	47444697
16	50133348	50133350	AA	--	15	GENIC	possibly homozygous	47444699
16	50133355	50133356	G	C	17	GENIC	possibly homozygous	47672592
16	50133367	50133368	G	C	19	GENIC	heterozygous	47672593
16	50133377	50133378	C	G	15	GENIC	homozygous	47444703
16	50133749	50133750	C	T	22	GENIC	homozygous	47672594
16	50134101	50134102	C	T	26	GENIC	homozygous	47672595
16	50134583	50134584	A	G	19	GENIC	homozygous	47444705
16	50135094	50135095	A	G	41	GENIC	homozygous	47444707
16	50135907	50135908	A	G	25	GENIC	homozygous	47444711
16	50136149	50136150	G	A	25	GENIC	homozygous	47444713
16	50136435	50136436	C	CT	18	GENIC	homozygous	47672596