chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41638342	41638343	G	A	7	GENIC	homozygous	115385544
12	41639041	41639042	T	A	11	GENIC	homozygous	115330976
12	41639316	41639317	G	T	8	GENIC	homozygous	115385546
12	41639321	41639322	A	T	9	GENIC	homozygous	115330978
12	41639322	41639323	T	A	9	GENIC	homozygous	115330980
12	41639604	41639605	A	C	15	GENIC	homozygous	115330982
12	41639605	41639606	C	A	13	GENIC	homozygous	115330984
12	41639833	41639834	C	T	11	GENIC	homozygous	115330986
12	41639834	41639835	T	C	10	GENIC	homozygous	115330988
12	41640806	41640807	C	G	5	GENIC	homozygous	115385548
12	41640845	41640846	G	A	9	GENIC	homozygous	115385550
12	41642447	41642448	C	T	9	GENIC	homozygous	115385552
12	41642508	41642509	T	C	15	GENIC	homozygous	115385554
12	41643842	41643843	A	C	9	GENIC	homozygous	115330992
12	41646090	41646091	G	C	9	GENIC	homozygous	115385556
12	41646188	41646189	T	C	7	GENIC	homozygous	115330998
12	41646445	41646446	T	C	10	GENIC	homozygous	115385558