chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64364919	64364920	T	C	22	GENIC	homozygous	116941610
10	64365280	64365281	T	C	19	GENIC	homozygous	116941612
10	64365297	64365298	T	C	21	GENIC	possibly homozygous	116941614
10	64367055	64367056	T	C	27	GENIC	homozygous	116941616
10	64367189	64367190	C	T	20	GENIC	homozygous	116941618
10	64367721	64367722	A	G	21	GENIC	homozygous	116941622
10	64367745	64367746	T	C	26	GENIC	homozygous	116617318
10	64371454	64371455	T	C	30	GENIC	homozygous	116941624
10	64371649	64371650	T	C	31	GENIC	homozygous	116941626
10	64372522	64372523	G	C	15	GENIC	homozygous	116941628
10	64373183	64373184	T	C	20	GENIC	homozygous	116941630
10	64374709	64374710	G	C	32	GENIC	homozygous	116941632
10	64374933	64374934	T	C	23	GENIC	homozygous	116941634
10	64375031	64375032	C	T	23	GENIC	homozygous	116941635
10	64375326	64375327	A	T	25	GENIC	homozygous	116941637
10	64375449	64375450	A	G	22	GENIC	homozygous	116941639