chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24720579	24720580	T	C	28	GENIC	homozygous	50135970
12	24720595	24720596	T	C	33	GENIC	homozygous	50135972
12	24720623	24720624	G	A	33	GENIC	homozygous	50135974
12	24720627	24720628	A	C	32	GENIC	homozygous	50135976
12	24720643	24720644	T	C	36	GENIC	homozygous	50135978
12	24720670	24720671	C	T	40	GENIC	homozygous	50135980
12	24720675	24720676	A	G	41	GENIC	homozygous	50135982
12	24720856	24720857	A	AACAC	7	GENIC	possibly homozygous	50135984
12	24720905	24720906	T	C	29	GENIC	homozygous	50135986
12	24721172	24721176	TGAT	----	40	GENIC	homozygous	50135988
12	24721182	24721183	G	A	41	GENIC	homozygous	50135990
12	24721524	24721525	A	G	40	GENIC	homozygous	50135992