chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10555351	10555352	G	A	36	GENIC	homozygous	116493268
10	10555353	10555354	T	C	35	GENIC	homozygous	116493270
10	10555618	10555619	A	G	45	GENIC	homozygous	116493272
10	10555624	10555625	G	A	46	GENIC	homozygous	116493274
10	10555632	10555633	A	G	47	GENIC	homozygous	116493276
10	10556032	10556033	C	T	38	GENIC	homozygous	116493278
10	10556058	10556059	C	T	54	GENIC	homozygous	116493280
10	10556108	10556109	T	C	63	GENIC	possibly homozygous	116493282
10	10556377	10556378	A	G	43	GENIC	homozygous	116493284
10	10557026	10557027	C	A	19	GENIC	homozygous	116493286
10	10557062	10557063	C	A	22	GENIC	homozygous	116493288
10	10558088	10558089	A	G	53	GENIC	homozygous	116493290
10	10559200	10559201	A	G	50	GENIC	homozygous	116493292
10	10560589	10560590	A	C	33	GENIC	homozygous	116493294
10	10561882	10561883	A	G	50	GENIC	homozygous	116493295
10	10562248	10562249	C	T	48	GENIC	homozygous	116493297
10	10562747	10562748	A	G	50	GENIC	homozygous	116493299