chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	40302072	40302073	G	A	71	GENIC	homozygous	140115073
17	40302604	40302605	C	T	52	GENIC	homozygous	140115074
17	40302936	40302937	T		42	GENIC	heterozygous	403413578
17	40303348	40303349	T	C	61	GENIC	homozygous	140115075
17	40303359	40303360	G	A	52	GENIC	homozygous	140115076
17	40303417	40303418	T	C	57	GENIC	homozygous	140115077
17	40303544	40303545	T	A	66	GENIC	homozygous	140115078
17	40304451	40304452	C	T	39	GENIC	homozygous	140115079
17	40305110	40305111	T	C	41	GENIC	homozygous	140115080
17	40305347	40305348	A	G	56	GENIC	homozygous	140115081
17	40305638	40305639	G	A	58	GENIC	homozygous	140115082
17	40305840	40305841	G	A	58	GENIC	homozygous	140115083
17	40306731	40306732	G	A	63	GENIC	possibly homozygous	140115084
17	40307279	40307280	A	G	61	GENIC	homozygous	140115085
17	40307359	40307360	G	A	72	GENIC	homozygous	140115086
17	40307449	40307450	A	G	66	GENIC	homozygous	140115087
17	40307976	40307977	T	C	50	GENIC	homozygous	140115088
17	40308546	40308547	G	A	49	GENIC	homozygous	140115089
17	40309341	40309342	G	C	38	GENIC	homozygous	140115090
17	40302936	40302937	T	G	42	GENIC	heterozygous	403413579
17	40304754	40304754		TA	52	GENIC	homozygous	140022448
17	40304018	40304019	T		60	GENIC	possibly homozygous	140022447
17	40304791	40304792	T		55	GENIC	possibly homozygous	140022449