chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	51517615	51517616	C	T	31	GENIC	homozygous	109279215
1	51518070	51518071	T	C	38	GENIC	homozygous	109279217
1	51518299	51518300	T	G	37	GENIC	homozygous	109279219
1	51518491	51518492	T	G	27	GENIC	homozygous	109279221
1	51518579	51518580	C	G	25	GENIC	homozygous	109279223
1	51519293	51519294	T	C	26	GENIC	homozygous	109279225
1	51520529	51520530	G	C	30	GENIC	homozygous	109279228
1	51520582	51520583	T	C	30	GENIC	homozygous	109279230
1	51521636	51521637	C	A	31	GENIC	possibly homozygous	108095750
1	51521880	51521881	C	A	29	GENIC	homozygous	109279232
1	51520540	51520541	A	G	29	GENIC	homozygous	108847664
1	51523441	51523442	G	C	31	GENIC	homozygous	108847667
1	51523455	51523456	T	C	32	GENIC	homozygous	108847668
1	51526033	51526034	T	C	30	GENIC	homozygous	108847672