chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	72960158	72960159	G	T	16	GENIC	homozygous	120124845
2	72960159	72960160	G	T	16	GENIC	homozygous	120124846
2	72960160	72960161	C	T	16	GENIC	homozygous	120124847
2	72960178	72960179	G	T	13	GENIC	homozygous	120124848
2	72960322	72960323	T	G	10	GENIC	homozygous	120124849
2	72960566	72960567	G	C	16	GENIC	homozygous	120124850
2	72961051	72961052	T	C	21	GENIC	homozygous	109828250
2	72961115	72961116	C	T	19	GENIC	homozygous	109828251
2	72961119	72961120	C	T	18	GENIC	homozygous	109828252
2	72961190	72961191	A	T	13	GENIC	homozygous	109828253
2	72961242	72961243	T	A	16	GENIC	homozygous	109828254
2	72961717	72961718	T	A	18	GENIC	homozygous	109828256
2	72961988	72961989	A	T	15	GENIC	homozygous	109828257
2	72962005	72962006	T	C	16	GENIC	homozygous	109828258
2	72962087	72962088	A	G	14	GENIC	homozygous	109828259
2	72962144	72962145	A	G	9	GENIC	homozygous	109828260
2	72963431	72963432	A	C	39	GENIC	homozygous	109828261
2	72963520	72963521	C	T	58	GENIC	homozygous	109828262