chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63664778	63664779	T	C	14	GENIC	homozygous	116940595
10	63666343	63666344	A	G	26	GENIC	homozygous	116616342
10	63666795	63666796	C	T	19	GENIC	possibly homozygous	117219630
10	63666799	63666800	C	G	19	GENIC	possibly homozygous	118041271
10	63667125	63667126	T	C	27	GENIC	homozygous	116940597
10	63667658	63667659	G	A	28	GENIC	homozygous	116791495
10	63669171	63669172	T	C	23	GENIC	homozygous	116616344
10	63672834	63672835	A	T	26	GENIC	homozygous	117130906
10	63674014	63674015	C	T	37	GENIC	homozygous	116616346
10	63682057	63682058	T	C	8	GENIC	homozygous	116616358
10	63675161	63675162	A	G	16	GENIC	homozygous	117013222
10	63675236	63675237	A	G	17	GENIC	homozygous	117013223
10	63676355	63676356	T	G	15	GENIC	homozygous	116616348
10	63677706	63677707	A	T	17	GENIC	homozygous	116940601
10	63683053	63683054	G	A	17	GENIC	homozygous	116940603