chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17055975	17055976	C	A	9	GENIC	homozygous	117983027
10	17055979	17055980	G	A	8	GENIC	homozygous	117983028
10	17056085	17056086	A	C	40	GENIC	homozygous	117983029
10	17056255	17056256	G	C	3	GENIC	homozygous	117983030
10	17056315	17056316	T	G	18	GENIC	homozygous	117983031
10	17056414	17056415	G	T	17	GENIC	possibly homozygous	117983032
10	17062681	17062682	A	G	28	GENIC	homozygous	116500124
10	17060894	17060895	A	T	74	GENIC	homozygous	116500118
10	17062021	17062022	C	T	63	GENIC	possibly homozygous	116500120
10	17062061	17062062	C	A	52	GENIC	possibly homozygous	116500122
10	17062869	17062870	T	A	43	GENIC	homozygous	116500126
10	17063714	17063715	T	C	51	GENIC	possibly homozygous	116500128
10	17064815	17064816	G	T	40	GENIC	homozygous	116500130
10	17064871	17064872	A	C	29	GENIC	homozygous	116500132
10	17065542	17065543	G	A	42	GENIC	homozygous	116500134
10	17066175	17066176	G	A	43	GENIC	homozygous	116500136
10	17066770	17066771	C	T	50	GENIC	homozygous	117983033
10	17067098	17067099	T	C	47	GENIC	homozygous	116500138
10	17068065	17068066	G	A	22	GENIC	homozygous	116500140
10	17068411	17068412	T	C	45	GENIC	homozygous	116500142
10	17070925	17070926	G	A	41	GENIC	homozygous	116500150
10	17068423	17068424	G	T	47	GENIC	homozygous	116500144
10	17070257	17070258	T	C	52	GENIC	homozygous	116500146
10	17070526	17070527	G	A	54	GENIC	homozygous	116500148
10	17070937	17070938	A	G	41	GENIC	homozygous	116500152
10	17071105	17071106	G	A	54	GENIC	possibly homozygous	116500154
10	17072333	17072334	C	T	70	GENIC	homozygous	116500156
10	17072373	17072374	G	A	61	GENIC	homozygous	116500158
10	17072769	17072770	G	A	41	GENIC	homozygous	116500162
10	17073304	17073305	T	C	51	GENIC	homozygous	116500164
10	17073593	17073594	G	A	55	GENIC	possibly homozygous	116500166
10	17071368	17071369	C	G	40	GENIC	homozygous	117294339