chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	107704022	107704023	C	A	43	GENIC	heterozygous	134869199
13	107704024	107704025	G	A	44	GENIC	heterozygous	134869200
13	107704025	107704026	T	C	44	GENIC	heterozygous	134869201
13	107704029	107704030	C	A	43	GENIC	heterozygous	134869202
13	107704037	107704038	C	G	41	GENIC	heterozygous	134869203
13	107704042	107704043	A	T	41	GENIC	heterozygous	134869204
13	107704043	107704044	A	G	40	GENIC	heterozygous	134869205
13	107704054	107704055	T	G	40	GENIC	heterozygous	134869206
13	107704055	107704056	T	C	40	GENIC	heterozygous	134869207
13	107704072	107704073	C	G	42	GENIC	heterozygous	134377560
13	107704266	107704267	G	A	56	GENIC	heterozygous	123801663
13	107704275	107704276	A	G	53	GENIC	heterozygous	123801664
13	107714074	107714078	AAAT		31	GENIC	homozygous	132716387
13	107787626	107787627	T	G	14	GENIC	possibly homozygous	114859110
13	107787608	107787609	T	G	20	GENIC	possibly homozygous	118468078
13	107787614	107787615	T	G	20	GENIC	possibly homozygous	118468079
13	107871275	107871278	AGA		43	GENIC	heterozygous	129094584