chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51569350	51569351	T	C	25	GENIC	homozygous	114343549
13	51570456	51570457	G	C	4	GENIC	homozygous	118592050
13	51570492	51570493	A	T	21	GENIC	possibly homozygous	118592051
13	51570955	51570956	G	T	49	GENIC	possibly homozygous	114948165
13	51571484	51571485	G	T	52	GENIC	possibly homozygous	114948167
13	51571700	51571701	G	A	31	GENIC	possibly homozygous	114948171
13	51571801	51571802	A	G	43	GENIC	homozygous	114948173
13	51572378	51572379	G	A	41	GENIC	possibly homozygous	114948175
13	51572704	51572705	T	C	38	GENIC	homozygous	114948177
13	51572797	51572798	C	T	38	GENIC	possibly homozygous	114948179
13	51572840	51572841	C	T	45	GENIC	homozygous	114948181
13	51572967	51572968	C	T	43	GENIC	possibly homozygous	114948183
13	51573243	51573244	A	G	54	GENIC	homozygous	114948185
13	51573704	51573705	C	T	58	GENIC	possibly homozygous	114948187
13	51576416	51576417	T	C	51	GENIC	possibly homozygous	114343551
13	51577010	51577011	T	C	45	GENIC	possibly homozygous	114343553
13	51577397	51577398	C	T	61	GENIC	homozygous	114948189
13	51577537	51577538	C	T	65	GENIC	homozygous	114948191