chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	50326033	50326034	A	T	30	GENIC	heterozygous	154096342
3	50326033	50326034	A		30	GENIC	possibly homozygous	403063410
3	50326035	50326036	A	T	30	GENIC	heterozygous	403063411
3	50326035	50326036	A		30	GENIC	possibly homozygous	403063412
3	50326037	50326038	A	T	30	GENIC	heterozygous	403063413
3	50326037	50326038	A		30	GENIC	possibly homozygous	403063414
3	50344129	50344130	G		14	GENIC	heterozygous	403984651
3	50344129	50344130	G	C	14	GENIC	heterozygous	403984652
3	50344131	50344132	G		14	GENIC	heterozygous	403984653
3	50344131	50344132	G	C	14	GENIC	heterozygous	403984654
3	50347929	50347931	AT		22	GENIC	heterozygous	140985746
3	50347931	50347932	A	C	22	GENIC	heterozygous	403063420
3	50347931	50347932	A		22	GENIC	heterozygous	403063421
3	50347933	50347934	G	C	22	GENIC	heterozygous	403063422
3	50347933	50347934	G		22	GENIC	heterozygous	403063423
3	50347935	50347936	G		23	GENIC	heterozygous	403063424
3	50347935	50347936	G	C	23	GENIC	heterozygous	403063425
3	50436945	50436946	T		30	GENIC	heterozygous	403063449
3	50436945	50436946	T	G	30	GENIC	possibly homozygous	403063450