chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94203861	94203862	T	C	38	GENIC	homozygous	51548257
10	94204870	94204871	A	G	57	GENIC	possibly homozygous	51548258
10	94207676	94207677	A	T	33	GENIC	homozygous	51548260
10	94207678	94207679	G	T	33	GENIC	homozygous	51548261
10	94207970	94207971	T	G	39	GENIC	homozygous	51548262
10	94208061	94208065	CCCC	----	42	GENIC	homozygous	51548263
10	94208594	94208595	T	C	36	GENIC	homozygous	51548264
10	94209458	94209459	A	C	24	GENIC	homozygous	51548265
10	94209473	94209474	C	T	28	GENIC	homozygous	51548266
10	94209916	94209917	G	A	41	GENIC	homozygous	51548267
10	94209997	94209999	AG	--	43	GENIC	homozygous	51548268
10	94211632	94211633	G	T	20	GENIC	homozygous	51746431