chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	159318277	159318278	T		13	GENIC	homozygous	127947647
3	159318305	159318310	GTCCC		14	GENIC	homozygous	127947648
3	159318313	159318314	G		14	GENIC	homozygous	127947649
3	159318321	159318322	G	T	13	GENIC	homozygous	119915027
3	159318325	159318325		C	13	GENIC	homozygous	127947650
3	159318333	159318333		GC	11	GENIC	homozygous	127947651
3	159318338	159318338		C	10	GENIC	homozygous	127947652
3	159318356	159318356		G	9	GENIC	homozygous	127947653
3	159318361	159318361		G	8	GENIC	homozygous	127947654
3	159318371	159318371		A	7	GENIC	homozygous	127947655
3	159318379	159318380	A		4	GENIC	homozygous	127947656
3	159318606	159318607	G		5	GENIC	homozygous	127947657
3	159318642	159318645	CAG		7	GENIC	homozygous	127947658
3	159318654	159318655	G		8	GENIC	homozygous	127947659
3	159318664	159318664		G	8	GENIC	homozygous	127947660
3	159318667	159318667		A	8	GENIC	homozygous	127947661
3	159318684	159318684		A	8	GENIC	homozygous	127947662
3	159318727	159318727		G	8	GENIC	homozygous	127947663
3	159318793	159318794	A		8	GENIC	homozygous	127947664
3	159318795	159318796	C		8	GENIC	homozygous	127947665
3	159318833	159318834	G	A	15	GENIC	homozygous	111789514
3	159318918	159318919	G		15	GENIC	homozygous	127947666
3	159318957	159318957		C	16	GENIC	homozygous	127947667
3	159318975	159318976	G		11	GENIC	homozygous	127947668
3	159319013	159319014	T	C	12	GENIC	homozygous	112045325
3	159319014	159319015	G	T	12	GENIC	homozygous	112045326
3	159319017	159319018	G		11	GENIC	homozygous	127947669
3	159325938	159325938		G	9	GENIC	homozygous	127947670
3	159325940	159325941	T	A	9	GENIC	homozygous	111789516