chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	165190190	165190192	GT		55	GENIC	possibly homozygous	130826409
1	165190354	165190355	G	A	63	GENIC	homozygous	108954221
1	165190647	165190648	C	T	64	GENIC	homozygous	108954222
1	165191345	165191346	G	C	51	GENIC	homozygous	108954224
1	165192122	165192123	T	C	53	GENIC	homozygous	108954226
1	165192177	165192178	C	T	63	GENIC	homozygous	108954227
1	165192291	165192292	C		57	GENIC	homozygous	130826410
1	165192295	165192296	A	C	56	GENIC	homozygous	108954228
1	165192330	165192330		GTCA	53	GENIC	homozygous	130826411
1	165191196	165191197	G	C	30	GENIC	homozygous	130847424
1	165193080	165193081	G	A	67	GENIC	homozygous	108954229
1	165193885	165193886	C	T	49	GENIC	homozygous	108954230
1	165194351	165194352	C	T	48	GENIC	homozygous	108954231
1	165195657	165195658	C	T	52	GENIC	homozygous	108954232