chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94203861	94203862	T	C	37	GENIC	homozygous	51548257
10	94204870	94204871	A	G	47	GENIC	heterozygous	51548258
10	94206345	94206346	C	T	28	GENIC	homozygous	51548259
10	94207676	94207677	A	T	37	GENIC	homozygous	51548260
10	94207678	94207679	G	T	39	GENIC	homozygous	51548261
10	94207713	94207714	G	A	39	GENIC	homozygous	52167448
10	94207970	94207971	T	G	32	GENIC	homozygous	51548262
10	94208061	94208065	CCCC	----	33	GENIC	homozygous	51548263
10	94208594	94208595	T	C	44	GENIC	homozygous	51548264
10	94209458	94209459	A	C	38	GENIC	homozygous	51548265
10	94209473	94209474	C	T	39	GENIC	homozygous	51548266
10	94209916	94209917	G	A	38	GENIC	homozygous	51548267
10	94209997	94209999	AG	--	38	GENIC	homozygous	51548268