chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	21527930	21527930		T	10	GENIC	homozygous	136551861
3	21528092	21528093	C	T	22	GENIC	homozygous	136653674
3	21528200	21528201	T	G	25	GENIC	homozygous	136653675
3	21528773	21528774	T	C	11	GENIC	homozygous	136653676
3	21528858	21528859	G	C	9	GENIC	heterozygous	404411605
3	21528856	21528857	G		7	GENIC	heterozygous	404411602
3	21528856	21528857	G	C	7	GENIC	heterozygous	404411603
3	21528858	21528859	G		9	GENIC	heterozygous	404411604
3	21528854	21528855	G	C	7	GENIC	possibly homozygous	403059143
3	21528860	21528861	G		9	GENIC	heterozygous	403059144
3	21528860	21528861	G	C	9	GENIC	heterozygous	403059145
3	21528902	21528902		AGCAA	7	GENIC	homozygous	136551862
3	21530761	21530762	A	G	16	GENIC	homozygous	136653677
3	21531615	21531616	C	T	15	GENIC	homozygous	136653678
3	21531805	21531806	C	T	4	GENIC	homozygous	136653679
3	21531878	21531879	A	T	16	GENIC	homozygous	136653680
3	21532252	21532253	T	C	18	GENIC	homozygous	136653681
3	21532326	21532327	C	A	19	GENIC	homozygous	136653682
3	21532708	21532709	T	C	20	GENIC	homozygous	136653683
3	21533043	21533044	A	C	23	GENIC	homozygous	136653684
3	21533230	21533230		T	12	GENIC	homozygous	136551863
3	21533821	21533822	A	G	19	GENIC	homozygous	136653685
3	21528854	21528855	G		7	GENIC	heterozygous	403059142