chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	70737465	70737466	G	A	26	GENIC	possibly homozygous	59816355
2	70738071	70738072	G	A	19	GENIC	homozygous	59816356
2	70738453	70738454	G	A	27	GENIC	homozygous	59816357
2	70738698	70738699	A	G	25	GENIC	homozygous	59816358
2	70738847	70738848	T	C	21	GENIC	homozygous	59816359
2	70739682	70739683	T	G	32	GENIC	homozygous	59816360
2	70739730	70739731	G	A	19	GENIC	homozygous	59816361
2	70739829	70739830	C	T	33	GENIC	homozygous	59816362
2	70740498	70740499	A	AC	31	GENIC	homozygous	59816363
2	70740515	70740516	T	TC	31	GENIC	homozygous	59816364
2	70740597	70740598	G	A	27	GENIC	homozygous	62152015
2	70740945	70740946	A	G	26	GENIC	homozygous	59816365
2	70740978	70740979	A	G	24	GENIC	homozygous	59816366
2	70741164	70741165	C	T	18	GENIC	homozygous	59816367
2	70741310	70741311	G	T	23	GENIC	homozygous	59816368
2	70741673	70741674	T	A	32	GENIC	homozygous	59816369
2	70741974	70741975	T	C	30	GENIC	homozygous	59816370
2	70742145	70742146	A	G	32	GENIC	homozygous	59816371
2	70742441	70742442	T	C	29	GENIC	homozygous	59816372
2	70742473	70742474	T	C	19	GENIC	possibly homozygous	59720819