chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	186872843	186872844	T	C	51	GENIC	homozygous	110166730
2	186873747	186873748	C	T	72	GENIC	possibly homozygous	110166731
2	186876262	186876263	A	G	58	GENIC	homozygous	110166732
2	186876448	186876449	T	C	44	GENIC	possibly homozygous	110166733
2	186876868	186876869	C	A	54	GENIC	homozygous	110166734
2	186878686	186878687	G	A	66	GENIC	homozygous	110166735
2	186879750	186879751	A	G	76	GENIC	homozygous	110166736
2	186882059	186882060	A	G	76	GENIC	homozygous	110166737
2	186882119	186882120	T	C	54	GENIC	homozygous	110166738
2	186885039	186885040	T	C	66	GENIC	homozygous	110166739
2	186885435	186885436	T	C	52	GENIC	homozygous	110166740
2	186885613	186885614	G	A	83	GENIC	possibly homozygous	110166741
2	186885877	186885878	T	C	48	GENIC	possibly homozygous	110166742
2	186885988	186885989	T	C	30	GENIC	homozygous	110166743
2	186886027	186886028	A	G	63	GENIC	homozygous	110166744
2	186886039	186886040	T	C	67	GENIC	homozygous	110166745
2	186886225	186886226	C	T	59	GENIC	homozygous	110166746
2	186886246	186886247	C	G	56	GENIC	possibly homozygous	110166747
2	186886253	186886254	A	G	59	GENIC	homozygous	110166748