chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10645703	10645704	G	A	21	GENIC	homozygous	110954702
17	10645896	10645897	G	A	30	GENIC	homozygous	110954704
17	10646352	10646353	G	A	17	GENIC	homozygous	110954706
17	10646814	10646815	A	G	17	GENIC	homozygous	111295107
17	10646952	10646953	C	G	18	GENIC	homozygous	111332287
17	10646956	10646957	G	T	18	GENIC	possibly homozygous	111332290
17	10647119	10647120	C	G	31	GENIC	homozygous	111231053
17	10647925	10647926	A	C	30	GENIC	possibly homozygous	119264032
17	10648004	10648005	T	G	29	GENIC	heterozygous	119264033
17	10648141	10648142	A	C	21	GENIC	heterozygous	111332294
17	10648166	10648167	A	G	17	GENIC	heterozygous	119264037
17	10648209	10648210	C	A	13	GENIC	possibly homozygous	111479557
17	10649195	10649196	T	C	20	GENIC	homozygous	111332297
17	10649494	10649495	G	A	18	GENIC	homozygous	119264040
17	10649498	10649499	C	T	16	GENIC	homozygous	119264041
17	10649513	10649514	A	G	13	GENIC	homozygous	119264042
17	10651417	10651418	C	A	31	GENIC	homozygous	110954708
17	10653576	10653577	G	A	26	GENIC	homozygous	110954710
17	10653719	10653720	G	A	12	GENIC	homozygous	119264046
17	10654030	10654031	G	T	21	GENIC	homozygous	110954712
17	10654031	10654032	C	T	21	GENIC	homozygous	110954714
17	10655656	10655657	A	G	20	GENIC	homozygous	110954715
17	10657097	10657098	G	A	14	GENIC	homozygous	110954717