chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219672785	219672786	T	TA	12	GENIC	homozygous	59401573
2	219672839	219672840	C	A	9	GENIC	homozygous	59401574
2	219672840	219672841	C	G	10	GENIC	homozygous	59401575
2	219674206	219674207	T	-	3	GENIC	homozygous	59401576
2	219702938	219702939	A	-	6	GENIC	heterozygous	60302090
2	219707405	219707406	A	-	8	GENIC	heterozygous	60302092
2	219712809	219712810	G	GT	19	GENIC	possibly homozygous	59401659
2	219712854	219712855	C	-	1	GENIC	homozygous	59401660
2	219712892	219712893	G	GT	2	GENIC	homozygous	59401663
2	219712911	219712912	C	-	10	GENIC	homozygous	59401664
2	219714349	219714350	G	-	18	GENIC	homozygous	59401667
2	219714353	219714354	T	TTA	19	GENIC	possibly homozygous	59401668
2	219734058	219734059	G	GT	3	GENIC	heterozygous	59401722
2	219755970	219755974	AATG	----	2	GENIC	heterozygous	60549144
2	219764643	219764644	C	CTG	3	GENIC	heterozygous	59401757
2	219765228	219765229	T	-	2	GENIC	heterozygous	59774584