chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	81222395	81222396	G		29	GENIC	heterozygous	403978901
2	81222395	81222396	G	C	29	GENIC	heterozygous	403978902
2	81295357	81295358	G		6	GENIC	heterozygous	403007645
2	81295357	81295358	G	C	6	GENIC	heterozygous	403007646
2	81295359	81295360	G		9	GENIC	heterozygous	403007647
2	81295359	81295360	G	C	9	GENIC	heterozygous	403007648
2	81295361	81295362	G		10	GENIC	heterozygous	403007649
2	81295361	81295362	G	C	10	GENIC	heterozygous	403007650
2	81312059	81312060	G		24	GENIC	heterozygous	403007657
2	81312059	81312060	G	C	24	GENIC	heterozygous	403007658
2	81312059	81312060	G	A	24	GENIC	heterozygous	403007659
2	81378917	81378918	T	G	11	GENIC	heterozygous	153969631
2	81378917	81378918	T		11	GENIC	homozygous	404594806
2	81423811	81423812	G	A	21	GENIC	homozygous	136171328
2	81483871	81483872	C		7	GENIC	heterozygous	403007688
2	81483871	81483872	C	T	7	GENIC	heterozygous	403007689
2	81487030	81487031	A		13	GENIC	heterozygous	403555751
2	81487030	81487031	A	T	13	GENIC	heterozygous	403555752
2	81487032	81487033	A		13	GENIC	heterozygous	403555753
2	81487032	81487033	A	T	13	GENIC	heterozygous	403555754
2	81519978	81519979	A	G	38	GENIC	homozygous	136171620
2	81519986	81519987	A	G	41	GENIC	homozygous	136171621
2	81519991	81519992	A	G	42	GENIC	homozygous	136171622
2	81520021	81520022	A		23	GENIC	heterozygous	403007699
2	81520021	81520022	A	G	23	GENIC	homozygous	403007700
2	81551832	81551833	C	A	26	GENIC	homozygous	136171732
2	81678785	81678786	A	G	31	GENIC	possibly homozygous	136172091
2	81812393	81812394	C		16	GENIC	heterozygous	140969065
2	81519998	81520002	AAAG		22	GENIC	homozygous	140969064
2	81812393	81812394	C	T	16	GENIC	heterozygous	403763089
2	81812395	81812396	C		16	GENIC	heterozygous	140969066
2	81871692	81871693	C		29	GENIC	heterozygous	403555776
2	81941746	81941747	C	T	33	GENIC	heterozygous	153975297
2	81941746	81941747	C		33	GENIC	heterozygous	403007789
2	81993970	81993971	T	C	45	GENIC	possibly homozygous	136172803
2	81871692	81871693	C	A	29	GENIC	possibly homozygous	140979441