chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17060894	17060895	A	T	29	GENIC	homozygous	116500118
10	17062021	17062022	C	T	22	GENIC	homozygous	116500120
10	17062061	17062062	C	A	28	GENIC	homozygous	116500122
10	17062681	17062682	A	G	24	GENIC	possibly homozygous	116500124
10	17062869	17062870	T	A	26	GENIC	homozygous	116500126
10	17063714	17063715	T	C	29	GENIC	homozygous	116500128
10	17064815	17064816	G	T	13	GENIC	possibly homozygous	116500130
10	17064871	17064872	A	C	20	GENIC	homozygous	116500132
10	17065542	17065543	G	A	16	GENIC	homozygous	116500134
10	17066175	17066176	G	A	28	GENIC	homozygous	116500136
10	17067098	17067099	T	C	21	GENIC	homozygous	116500138
10	17068065	17068066	G	A	14	GENIC	homozygous	116500140
10	17068411	17068412	T	C	27	GENIC	homozygous	116500142
10	17068423	17068424	G	T	27	GENIC	homozygous	116500144
10	17070257	17070258	T	C	20	GENIC	homozygous	116500146
10	17070526	17070527	G	A	28	GENIC	homozygous	116500148
10	17070925	17070926	G	A	28	GENIC	homozygous	116500150
10	17070937	17070938	A	G	30	GENIC	homozygous	116500152
10	17071105	17071106	G	A	31	GENIC	homozygous	116500154
10	17072333	17072334	C	T	34	GENIC	homozygous	116500156
10	17072373	17072374	G	A	34	GENIC	homozygous	116500158
10	17072726	17072727	T	C	26	GENIC	homozygous	116500160
10	17072769	17072770	G	A	20	GENIC	homozygous	116500162
10	17073304	17073305	T	C	29	GENIC	homozygous	116500164
10	17073593	17073594	G	A	31	GENIC	homozygous	116500166