chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39898254	39898255	C	CCAGGG	13	GENIC	homozygous	50202053
12	39899350	39899351	C	T	20	GENIC	homozygous	50421974
12	39901800	39901801	T	C	17	GENIC	homozygous	50202055
12	39902085	39902086	T	TG	20	GENIC	homozygous	50202057
12	39902097	39902098	T	C	17	GENIC	homozygous	50202059
12	39903494	39903495	G	GCCCC	2	GENIC	homozygous	50543404
12	39904376	39904378	CA	--	8	GENIC	homozygous	50543405
12	39904571	39904572	G	A	23	GENIC	homozygous	50693597
12	39908814	39908815	G	-	25	GENIC	homozygous	50202073
12	39909075	39909076	T	C	31	GENIC	homozygous	50202078
12	39918294	39918295	A	G	29	GENIC	homozygous	50693600
12	39919930	39919931	C	CA	21	GENIC	possibly homozygous	50629186
12	39923376	39923377	C	A	5	GENIC	heterozygous	50543408