chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59805031	59805032	T	C	41	INTERGENIC	homozygous	51466310
10	59809502	59809503	T	C	43	INTERGENIC	possibly homozygous	51466311
10	59811017	59811018	C	A	10	INTERGENIC	heterozygous	51466312
10	59811315	59811316	G	A	25	INTERGENIC	homozygous	51466313
10	59812386	59812387	G	T	40	INTERGENIC	homozygous	51466314
10	59813202	59813203	G	A	42	INTERGENIC	possibly homozygous	51466315
10	59813660	59813661	T	C	38	INTERGENIC	possibly homozygous	51466316
10	59814653	59814654	C	G	23	GENIC	homozygous	51466317
10	59814956	59814957	C	CAT	13	GENIC	homozygous	51466318
10	59820239	59820240	G	A	39	GENIC	heterozygous	51466319
10	59820257	59820258	T	A	41	GENIC	heterozygous	51466320
10	59820306	59820307	T	TC	36	GENIC	homozygous	51466321
10	59820410	59820411	T	G	19	INTERGENIC	homozygous	51466322
10	59820416	59820417	T	TA	18	INTERGENIC	homozygous	51466323
10	59821435	59821436	T	C	28	INTERGENIC	homozygous	51466324
10	59821864	59821865	C	T	12	INTERGENIC	homozygous	51466325
10	59822463	59822464	C	G	29	INTERGENIC	possibly homozygous	51466326
10	59823741	59823742	A	C	28	INTERGENIC	homozygous	51466327