chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	187162200	187162201	T	A	10	GENIC	homozygous	111278050
2	187162356	187162357	T	C	7	GENIC	homozygous	111278052
2	187162932	187162933	G	A	9	GENIC	homozygous	111278054
2	187163386	187163387	A	T	9	GENIC	homozygous	110803641
2	187163719	187163720	T	C	8	GENIC	homozygous	110803642
2	187164064	187164065	T	G	10	GENIC	homozygous	110166992
2	187164868	187164869	T	C	7	GENIC	homozygous	110166993
2	187164913	187164914	G	A	7	GENIC	homozygous	111278056
2	187165065	187165066	A	G	11	GENIC	homozygous	110166994
2	187165764	187165765	G	A	9	GENIC	homozygous	110803645
2	187166445	187166446	C	T	7	GENIC	homozygous	111278058
2	187167603	187167604	A	G	4	GENIC	homozygous	110166997
2	187168259	187168260	G	A	15	GENIC	homozygous	111278060
2	187168914	187168915	A	G	9	GENIC	homozygous	110166998
2	187169697	187169698	T	G	4	GENIC	homozygous	110167001
2	187170415	187170416	A	G	9	GENIC	homozygous	111278062
2	187170663	187170664	A	C	10	GENIC	homozygous	110167002
2	187171916	187171917	A	G	9	GENIC	homozygous	110167004
2	187172861	187172862	A	G	13	GENIC	homozygous	110167005
2	187173979	187173980	C	T	10	GENIC	homozygous	111278064
2	187176239	187176240	T	C	13	GENIC	homozygous	110167010
2	187177411	187177412	G	A	6	GENIC	homozygous	111278065
2	187180169	187180170	A	T	13	GENIC	homozygous	110167020
2	187181292	187181293	A	G	7	GENIC	homozygous	110167025