chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64364919	64364920	T	C	28	GENIC	homozygous	116941610
10	64365280	64365281	T	C	19	GENIC	homozygous	116941612
10	64365297	64365298	T	C	21	GENIC	homozygous	116941614
10	64367055	64367056	T	C	26	GENIC	homozygous	116941616
10	64367189	64367190	C	T	27	GENIC	homozygous	116941618
10	64367642	64367643	G	A	17	GENIC	homozygous	116941620
10	64367702	64367703	G	T	25	GENIC	homozygous	116617316
10	64367721	64367722	A	G	25	GENIC	homozygous	116941622
10	64367745	64367746	T	C	25	GENIC	homozygous	116617318
10	64371454	64371455	T	C	29	GENIC	homozygous	116941624
10	64371649	64371650	T	C	13	GENIC	homozygous	116941626
10	64372522	64372523	G	C	19	GENIC	homozygous	116941628
10	64373183	64373184	T	C	27	GENIC	homozygous	116941630
10	64374709	64374710	G	C	28	GENIC	homozygous	116941632
10	64374933	64374934	T	C	18	GENIC	homozygous	116941634
10	64375031	64375032	C	T	25	GENIC	homozygous	116941635
10	64375326	64375327	A	T	26	GENIC	homozygous	116941637
10	64375449	64375450	A	G	13	GENIC	homozygous	116941639