chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	219872613	219872614	C	CA	8	GENIC	heterozygous	59402045
2	219872991	219872992	G	A	6	GENIC	homozygous	59402046
2	219873944	219873945	A	C	7	GENIC	heterozygous	59402047
2	219874267	219874268	G	T	14	GENIC	homozygous	59402048
2	219874301	219874302	C	A	12	GENIC	homozygous	59402049
2	219875510	219875511	C	CATGG	3	GENIC	homozygous	59402050
2	219876048	219876049	G	A	12	GENIC	homozygous	59402051
2	219876774	219876775	G	A	7	GENIC	possibly homozygous	59402052
2	219876898	219876899	C	T	13	GENIC	homozygous	59402053
2	219877288	219877289	A	G	6	GENIC	heterozygous	59402054
2	219878353	219878354	G	GTCTGTCTGTC	4	GENIC	heterozygous	59402057
2	219878708	219878709	T	C	15	GENIC	possibly homozygous	59402059
2	219879040	219879041	C	T	10	GENIC	homozygous	59402060
2	219879547	219879548	T	C	14	GENIC	homozygous	59402061
2	219879575	219879576	A	G	12	GENIC	heterozygous	59402062
2	219879890	219879891	T	G	15	GENIC	homozygous	59402063
2	219879908	219879909	C	T	8	GENIC	homozygous	59402064
2	219881186	219881187	A	T	12	GENIC	homozygous	59402068
2	219881254	219881255	A	AT	3	GENIC	homozygous	59402069
2	219881535	219881536	C	G	7	GENIC	homozygous	59402070
2	219881838	219881839	G	T	6	GENIC	homozygous	59402071
2	219883325	219883326	G	T	6	GENIC	heterozygous	59402078
2	219883643	219883644	T	G	15	GENIC	homozygous	59402079
2	219884055	219884056	C	T	5	GENIC	homozygous	59402080
2	219884245	219884246	T	C	11	GENIC	heterozygous	59402081
2	219884451	219884452	T	C	5	GENIC	homozygous	59402082
2	219885394	219885395	A	G	15	GENIC	homozygous	59402085
2	219885501	219885502	A	G	9	GENIC	possibly homozygous	59402086