chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	186872804	186872805	G	A	41	GENIC	possibly homozygous	110803607
2	186872843	186872844	T	C	33	GENIC	homozygous	110166730
2	186874400	186874401	A	G	50	GENIC	homozygous	110803608
2	186876262	186876263	A	G	38	GENIC	homozygous	110166732
2	186876868	186876869	C	A	35	GENIC	homozygous	110166734
2	186878686	186878687	G	A	48	GENIC	possibly homozygous	110166735
2	186879750	186879751	A	G	69	GENIC	homozygous	110166736
2	186882059	186882060	A	G	56	GENIC	homozygous	110166737
2	186882119	186882120	T	C	49	GENIC	homozygous	110166738
2	186884719	186884720	C	T	49	GENIC	homozygous	110803609
2	186885039	186885040	T	C	36	GENIC	homozygous	110166739
2	186885435	186885436	T	C	39	GENIC	homozygous	110166740
2	186885877	186885878	T	C	44	GENIC	homozygous	110166742
2	186885988	186885989	T	C	42	GENIC	homozygous	110166743
2	186886027	186886028	A	G	50	GENIC	homozygous	110166744
2	186886246	186886247	C	G	36	GENIC	homozygous	110166747
2	186886253	186886254	A	G	36	GENIC	homozygous	110166748
2	186886262	186886263	T	C	36	GENIC	possibly homozygous	110803610
2	186886570	186886571	A	G	42	GENIC	homozygous	110803611
2	186887279	186887280	G	A	48	GENIC	possibly homozygous	110803612