chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	52200591	52200592	T	G	12	GENIC	possibly homozygous	116884953
10	52210673	52210674	T	C	29	GENIC	homozygous	116779218
10	52210674	52210675	C	A	30	GENIC	homozygous	116779220
10	52210699	52210700	G	A	30	GENIC	homozygous	116779222
10	52210707	52210708	C	A	33	GENIC	homozygous	116779224
10	52210713	52210714	T	A	30	GENIC	homozygous	116779226
10	52210720	52210721	T	A	29	GENIC	homozygous	116779228
10	52210728	52210729	G	A	29	GENIC	homozygous	116779230
10	52210736	52210737	G	A	28	GENIC	homozygous	116596137
10	52284208	52284209	G	A	21	GENIC	homozygous	116596336