chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39898254	39898255	C	CCAGGG	10	GENIC	homozygous	50202053
12	39901800	39901801	T	C	9	GENIC	homozygous	50202055
12	39902085	39902086	T	TG	3	GENIC	homozygous	50202057
12	39902097	39902098	T	C	5	GENIC	homozygous	50202059
12	39903394	39903395	G	-	7	GENIC	homozygous	50381013
12	39903494	39903495	G	GCCCC	1	GENIC	homozygous	50543404
12	39904376	39904378	CA	--	4	GENIC	homozygous	50543405
12	39906747	39906748	C	T	21	GENIC	homozygous	50381014
12	39907081	39907082	T	C	28	GENIC	homozygous	50381015
12	39907602	39907603	T	C	20	GENIC	homozygous	50381016
12	39907932	39907933	G	A	32	GENIC	homozygous	50381017
12	39908838	39908846	TGGAGGCA	--------	17	GENIC	homozygous	50202075
12	39909075	39909076	T	C	18	GENIC	homozygous	50202078
12	39911917	39911918	A	ATGTG	3	GENIC	heterozygous	50604470
12	39920933	39920934	G	A	22	GENIC	homozygous	50381020
12	39923376	39923377	C	A	9	GENIC	homozygous	50543408