chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	45024852	45024853	A	G	59	GENIC	homozygous	130117595
20	45025806	45025807	C	T	50	GENIC	homozygous	148988079
20	45027925	45027925		A	12	GENIC	homozygous	130001196
20	45027994	45027995	G	A	39	GENIC	homozygous	130117599
20	45028744	45028745	G	A	51	GENIC	homozygous	149192911
20	45029066	45029067	G	A	24	GENIC	homozygous	148988082
20	45029120	45029122	TG		35	GENIC	homozygous	148983457
20	45029210	45029211	A	T	34	GENIC	possibly homozygous	130117601
20	45029211	45029212	T	C	35	GENIC	possibly homozygous	130117602
20	45032234	45032234		TATTT	63	GENIC	homozygous	130001198
20	45032995	45032996	C	T	57	GENIC	homozygous	149192913
20	45029317	45029318	T	G	36	GENIC	possibly homozygous	130117603
20	45029532	45029533	T	G	54	GENIC	possibly homozygous	149192912