chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62353111	62353112	T	A	49	GENIC	homozygous	51472191
10	62353116	62353117	C	A	53	GENIC	homozygous	51472192
10	62354582	62354583	T	C	40	GENIC	homozygous	51472193
10	62354667	62354668	A	AG	6	GENIC	heterozygous	51472194
10	62354700	62354701	A	T	31	GENIC	homozygous	51472195
10	62354872	62354873	C	T	42	GENIC	homozygous	51472196
10	62357013	62357014	T	G	24	GENIC	heterozygous	51472197
10	62358398	62358399	C	-	5	GENIC	heterozygous	51472198
10	62359304	62359305	G	-	29	GENIC	homozygous	51472199
10	62359322	62359323	A	ACG	17	GENIC	homozygous	51472200
10	62359353	62359355	CT	--	33	GENIC	homozygous	51472201
10	62359366	62359367	A	C	43	GENIC	possibly homozygous	51472202
10	62359416	62359417	G	C	61	GENIC	homozygous	51472203
10	62359519	62359520	G	A	59	GENIC	homozygous	51472204
10	62359892	62359893	G	A	67	GENIC	possibly homozygous	51472205