chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	15653132	15653133	G	A	63	GENIC	homozygous	64688224
17	15655663	15655664	G	C	61	GENIC	homozygous	64298111
17	15660626	15660627	G	A	46	GENIC	possibly homozygous	64688226
17	15664932	15664933	T	C	52	GENIC	homozygous	64688228
17	15665187	15665188	T	C	44	GENIC	homozygous	64298123
17	15665474	15665475	G	T	46	GENIC	homozygous	64298125
17	15665543	15665544	C	G	69	GENIC	possibly homozygous	64298127
17	15665551	15665552	C	T	65	GENIC	homozygous	64298129
17	15665573	15665574	G	T	59	GENIC	homozygous	64298131
17	15665653	15665654	A	G	58	GENIC	homozygous	64298133
17	15665709	15665710	C	T	59	GENIC	possibly homozygous	64298135
17	15665764	15665765	G	C	61	GENIC	homozygous	64298137
17	15666513	15666514	G	A	53	GENIC	homozygous	64298139
17	15666543	15666544	A	G	50	GENIC	homozygous	64298141
17	15666712	15666713	G	A	45	GENIC	homozygous	64298143
17	15666751	15666752	T	G	40	GENIC	homozygous	64298145
17	15666893	15666894	G	A	50	GENIC	possibly homozygous	64298151
17	15666960	15666961	C	T	66	GENIC	homozygous	64298153
17	15667040	15667041	T	C	46	GENIC	homozygous	64298155
17	15667214	15667215	T	G	51	GENIC	homozygous	64298157
17	15667370	15667371	T	C	44	GENIC	homozygous	64298159
17	15667445	15667446	A	G	41	GENIC	homozygous	64298161
17	15667492	15667493	G	T	51	GENIC	homozygous	64298163
17	15667569	15667570	A	G	58	GENIC	homozygous	64298165
17	15667653	15667654	G	T	55	GENIC	homozygous	64298167
17	15667743	15667744	A	G	43	GENIC	possibly homozygous	64298169
17	15667852	15667853	A	G	44	GENIC	homozygous	64298171
17	15667955	15667956	G	A	44	GENIC	possibly homozygous	64298173
17	15668478	15668479	T	C	25	GENIC	possibly homozygous	64298175