chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41024735	41024736	A	G	42	GENIC	homozygous	114768830
6	41025684	41025685	A	G	55	GENIC	homozygous	114768832
6	41026772	41026773	G	T	58	GENIC	homozygous	114768834
6	41028519	41028520	G	A	28	GENIC	heterozygous	114768836
6	41028521	41028522	G	A	28	GENIC	heterozygous	114768838
6	41029522	41029523	G	A	35	GENIC	possibly homozygous	114768840
6	41029834	41029835	C	T	40	GENIC	homozygous	114768842
6	41030649	41030650	G	A	40	GENIC	homozygous	114768844
6	41030931	41030932	G	C	55	GENIC	homozygous	114768846
6	41030942	41030943	G	A	56	GENIC	possibly homozygous	114768848
6	41031539	41031540	T	C	43	GENIC	homozygous	114768850
6	41031547	41031548	G	A	41	GENIC	homozygous	114768852