chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219872613	219872614	C	CA	23	GENIC	homozygous	59402045
2	219872991	219872992	G	A	28	GENIC	homozygous	59402046
2	219873795	219873796	C	T	36	GENIC	homozygous	60683662
2	219874267	219874268	G	T	24	GENIC	homozygous	59402048
2	219874301	219874302	C	A	32	GENIC	homozygous	59402049
2	219875510	219875511	C	CATGG	24	GENIC	homozygous	59402050
2	219876048	219876049	G	A	20	GENIC	homozygous	59402051
2	219877051	219877052	G	A	24	GENIC	homozygous	60683664
2	219877288	219877289	A	G	24	GENIC	homozygous	59402054
2	219878708	219878709	T	C	38	GENIC	homozygous	59402059
2	219879040	219879041	C	T	33	GENIC	homozygous	59402060
2	219879683	219879684	G	A	32	GENIC	homozygous	60683666
2	219880699	219880700	G	A	43	GENIC	homozygous	59402065
2	219881186	219881187	A	T	33	GENIC	homozygous	59402068
2	219881509	219881510	A	-	45	GENIC	homozygous	60683668
2	219881934	219881935	G	A	37	GENIC	homozygous	60683670
2	219883037	219883038	G	A	19	GENIC	homozygous	60683672
2	219883238	219883239	C	CGT	21	GENIC	homozygous	59402076
2	219883643	219883644	T	G	32	GENIC	homozygous	59402079
2	219883985	219883986	A	-	23	GENIC	possibly homozygous	60161716
2	219884245	219884246	T	C	20	GENIC	homozygous	59402081
2	219885394	219885395	A	G	50	GENIC	homozygous	59402085
2	219885501	219885502	A	G	42	GENIC	homozygous	59402086
2	219875591	219875592	G	C	14	GENIC	homozygous	61774706
2	219883301	219883311	GTGTGTGCGC	----------	22	GENIC	possibly homozygous	61774708