chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	92025498	92025499	C	T	36	GENIC	homozygous	116952584
10	92026302	92026303	C	T	48	GENIC	homozygous	116952586
10	92026777	92026778	C	T	49	GENIC	homozygous	116952588
10	92028059	92028060	T	A	49	GENIC	homozygous	116679089
10	92028106	92028107	A	G	44	GENIC	homozygous	116952590
10	92029769	92029770	A	G	43	GENIC	homozygous	116679093
10	92029782	92029783	G	A	44	GENIC	homozygous	116906399
10	92029897	92029898	A	G	42	GENIC	homozygous	116679097
10	92029899	92029900	G	T	42	GENIC	homozygous	116679099
10	92030733	92030734	T	C	54	GENIC	homozygous	116906403
10	92031000	92031001	T	A	52	GENIC	possibly homozygous	117328733
10	92031020	92031021	C	T	52	GENIC	homozygous	117020966
10	92031036	92031037	C	A	51	GENIC	possibly homozygous	118008159
10	92031353	92031354	A	T	40	GENIC	homozygous	118008160
10	92031467	92031468	G	C	52	GENIC	homozygous	116679107
10	92031653	92031654	T	C	54	GENIC	possibly homozygous	116822910
10	92032722	92032723	C	A	36	GENIC	homozygous	116952592
10	92032794	92032795	C	T	34	GENIC	homozygous	116679109
10	92033006	92033007	T	C	60	GENIC	homozygous	116679111
10	92034140	92034141	C	G	51	GENIC	homozygous	116679113
10	92034438	92034439	C	T	51	GENIC	homozygous	116952598
10	92035331	92035332	C	G	48	GENIC	homozygous	116822912
10	92037326	92037327	C	T	42	GENIC	homozygous	116952600
10	92037519	92037520	T	C	41	GENIC	homozygous	116679115
10	92039540	92039541	G	T	42	GENIC	possibly homozygous	116679121
10	92040134	92040135	C	T	54	GENIC	homozygous	116952602
10	92031231	92031232	G	A	51	GENIC	homozygous	117133888