chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	4902929	4902930	C	T	56	GENIC	homozygous	115199649
6	4904346	4904347	T	G	32	GENIC	homozygous	115199652
6	4905032	4905033	T	C	40	GENIC	homozygous	115199654
6	4905035	4905036	C	T	39	GENIC	homozygous	115199656
6	4905041	4905042	A	G	44	GENIC	homozygous	115199659
6	4906426	4906427	T	A	39	GENIC	possibly homozygous	115199661
6	4907228	4907229	T	C	39	GENIC	homozygous	114709712
6	4907247	4907248	G	T	36	GENIC	homozygous	115199666
6	4907888	4907889	A	T	36	GENIC	homozygous	115199668
6	4909611	4909612	T	C	49	GENIC	heterozygous	115199671
6	4910085	4910086	A	G	12	GENIC	possibly homozygous	115199673
6	4911144	4911145	A	T	39	GENIC	homozygous	115199676
6	4912066	4912067	G	T	49	GENIC	possibly homozygous	115199678
6	4912067	4912068	C	T	50	GENIC	possibly homozygous	115199681
6	4912208	4912209	T	G	54	GENIC	homozygous	115199683
6	4912655	4912656	A	C	49	GENIC	homozygous	115199686
6	4909662	4909663	T	G	74	GENIC	heterozygous	115488324