chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	96259700	96259701	T	C	1	GENIC	homozygous	64791687
17	96259893	96259894	C	A	13	GENIC	homozygous	64791691
17	96270994	96270995	A	C	11	GENIC	homozygous	64791699
17	96265011	96265012	A	G	19	GENIC	homozygous	64662763
17	96262563	96262564	T	C	23	GENIC	homozygous	64662760
17	96260713	96260714	G	A	8	GENIC	homozygous	64981215
17	96272490	96272491	T	G	11	GENIC	homozygous	64662772
17	96274995	96274996	A	G	30	GENIC	homozygous	64662775
17	96277559	96277560	C	T	30	GENIC	homozygous	64981216
17	96278864	96278865	T	C	22	GENIC	homozygous	64791705
17	96280638	96280639	T	C	38	GENIC	homozygous	64662778
17	96282588	96282589	A	G	23	GENIC	homozygous	64981218
17	96284614	96284615	C	T	13	GENIC	homozygous	64981219
17	96285770	96285771	C	T	25	GENIC	homozygous	64981220
17	96288754	96288755	C	T	21	GENIC	homozygous	64981221
17	96292262	96292263	T	C	23	GENIC	homozygous	64981222
17	96294168	96294169	A	G	26	GENIC	homozygous	64662789
17	96294235	96294236	C	T	16	GENIC	homozygous	64981223
17	96294616	96294617	T	A	24	GENIC	homozygous	64981224
17	96298344	96298345	A	G	36	GENIC	homozygous	64791737
17	96309640	96309641	T	G	29	GENIC	homozygous	64981225
17	96315813	96315814	G	A	24	GENIC	homozygous	64981226
17	96321720	96321721	G	A	17	GENIC	homozygous	64981227
17	96302609	96302610	C	T	21	GENIC	possibly homozygous	65050293