chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	101012053	101012054	T	C	17	GENIC	homozygous	57933259
3	101012109	101012110	C	G	20	GENIC	homozygous	58532847
3	101012178	101012179	T	C	29	GENIC	possibly homozygous	57933261
3	101013031	101013032	C	T	25	GENIC	heterozygous	58532848
3	101013065	101013066	T	C	24	GENIC	possibly homozygous	58532849
3	101013404	101013405	A	G	8	GENIC	possibly homozygous	57933263
3	101013993	101013994	C	T	21	GENIC	homozygous	58532850
3	101014127	101014128	T	-	10	GENIC	possibly homozygous	57933265
3	101016003	101016004	A	C	15	GENIC	possibly homozygous	58532855
3	101016195	101016196	G	A	8	GENIC	homozygous	58532856
3	101016254	101016255	A	G	5	GENIC	homozygous	58532857
3	101016588	101016589	G	A	17	GENIC	possibly homozygous	58532858
3	101016680	101016684	CAGG	----	5	GENIC	homozygous	58532859
3	101017491	101017492	C	T	26	GENIC	possibly homozygous	58532861