chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	2274967	2274968	G	A	46	GENIC	homozygous	142803610
1	2275150	2275151	G	A	46	GENIC	homozygous	146010601
1	2276434	2276435	C	A	50	GENIC	possibly homozygous	142803611
1	2288319	2288320	T	C	45	GENIC	homozygous	146010602
1	2288667	2288668	T		37	GENIC	possibly homozygous	146003461
1	2288830	2288831	A	G	48	GENIC	homozygous	146010603
1	2289109	2289110	A	G	39	GENIC	homozygous	142803613
1	2289987	2289988	C	T	42	GENIC	homozygous	142803614
1	2296138	2296139	G	A	54	GENIC	homozygous	142803616
1	2299936	2299937	T	C	49	GENIC	homozygous	142803617
1	2300078	2300079	T	A	54	GENIC	homozygous	142803618
1	2300994	2300994		GTATGTAT	42	GENIC	homozygous	146003462
1	2276529	2276530	A	G	52	GENIC	homozygous	135482931
1	2288667	2288668	T	A	37	GENIC	heterozygous	153786563
1	2286623	2286624	T		42	GENIC	possibly homozygous	142782026
1	2293952	2293952		A	51	GENIC	homozygous	142782027
1	2301380	2301381	T		18	GENIC	possibly homozygous	146331501
1	2301405	2301406	T		20	GENIC	heterozygous	402938835
1	2301405	2301406	T	C	20	GENIC	heterozygous	402938836
1	2301407	2301408	T		22	GENIC	heterozygous	402938837
1	2301407	2301408	T	C	22	GENIC	heterozygous	402938838
1	2301550	2301551	G	A	59	GENIC	homozygous	142803619
1	2303546	2303547	G	A	39	GENIC	homozygous	146010604