chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94104305	94104306	A	G	17	GENIC	heterozygous	51746290
10	94106576	94106577	G	A	20	GENIC	possibly homozygous	51746292
10	94106666	94106667	C	T	34	GENIC	homozygous	51746294
10	94109148	94109149	C	T	32	GENIC	homozygous	51548075
10	94109268	94109269	C	A	8	GENIC	homozygous	51746296
10	94109977	94109978	C	A	33	GENIC	possibly homozygous	51746298
10	94110757	94110758	C	T	21	GENIC	homozygous	51746300
10	94110867	94110868	A	T	15	GENIC	homozygous	51548077
10	94111288	94111289	T	G	15	GENIC	possibly homozygous	51548079
10	94111357	94111358	T	C	14	GENIC	possibly homozygous	51746302
10	94112025	94112026	C	A	21	GENIC	possibly homozygous	51746304
10	94112152	94112153	A	G	28	GENIC	homozygous	51548082
10	94114232	94114233	A	C	23	GENIC	homozygous	51746306
10	94114386	94114387	T	C	24	GENIC	possibly homozygous	51746308
10	94114615	94114616	G	A	23	GENIC	possibly homozygous	51746310
10	94115169	94115170	C	CAAAA	1	GENIC	homozygous	51746312
10	94115915	94115916	C	A	24	GENIC	homozygous	51746316
10	94116796	94116797	G	A	19	GENIC	homozygous	51548091
10	94117055	94117056	G	C	17	GENIC	possibly homozygous	51548092
10	94120334	94120336	AA	--	4	GENIC	homozygous	51746318
10	94125613	94125614	T	-	3	GENIC	homozygous	51548098