chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	62871149	62871150	G	C	38	GENIC	possibly homozygous	109789339
2	62874061	62874062	G	A	52	GENIC	homozygous	109789341
2	62874440	62874441	T	C	51	GENIC	homozygous	109789343
2	62875726	62875727	G	A	86	GENIC	homozygous	109789345
2	62875741	62875742	G	A	85	GENIC	homozygous	109789347
2	62875781	62875782	C	T	75	GENIC	homozygous	109789349
2	62875814	62875815	C	T	73	GENIC	homozygous	109789351
2	62875821	62875822	G	A	72	GENIC	homozygous	109789353
2	62876042	62876043	C	T	65	GENIC	homozygous	109789355
2	62876108	62876109	C	T	50	GENIC	homozygous	109789357
2	62876771	62876772	A	G	72	GENIC	homozygous	109789359
2	62876984	62876985	T	C	50	GENIC	homozygous	109789361
2	62877170	62877171	C	T	50	GENIC	possibly homozygous	109789363
2	62878600	62878601	C	T	54	GENIC	homozygous	109789365
2	62880994	62880995	T	C	28	GENIC	homozygous	109789367
2	62882228	62882229	C	T	76	GENIC	homozygous	109789369
2	62884586	62884587	C	T	61	GENIC	homozygous	109789371
2	62885082	62885083	C	T	58	GENIC	homozygous	109789373
2	62885177	62885178	A	C	61	GENIC	homozygous	109789375
2	62885431	62885432	G	T	59	GENIC	homozygous	109789377