chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64364919	64364920	T	C	34	GENIC	homozygous	116941610
10	64365297	64365298	T	C	19	GENIC	homozygous	116941614
10	64366762	64366763	G	T	21	GENIC	homozygous	117151271
10	64367055	64367056	T	C	18	GENIC	homozygous	116941616
10	64367189	64367190	C	T	30	GENIC	homozygous	116941618
10	64367642	64367643	G	A	16	GENIC	homozygous	116941620
10	64367721	64367722	A	G	25	GENIC	homozygous	116941622
10	64370122	64370123	G	T	29	GENIC	homozygous	117151272
10	64370126	64370127	G	A	29	GENIC	homozygous	117151273
10	64371454	64371455	T	C	43	GENIC	homozygous	116941624
10	64371649	64371650	T	C	34	GENIC	homozygous	116941626
10	64367702	64367703	G	T	28	GENIC	homozygous	116617316
10	64367745	64367746	T	C	21	GENIC	homozygous	116617318
10	64372522	64372523	G	C	17	GENIC	homozygous	116941628
10	64373146	64373147	T	C	22	GENIC	homozygous	117151274
10	64373183	64373184	T	C	28	GENIC	homozygous	116941630
10	64374933	64374934	T	C	29	GENIC	homozygous	116941634
10	64375326	64375327	A	T	30	GENIC	homozygous	116941637
10	64375449	64375450	A	G	21	GENIC	homozygous	116941639