chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109251327	109251328	T	G	21	GENIC	homozygous	51598955
10	109251526	109251529	CGG	---	16	GENIC	homozygous	51598956
10	109251765	109251766	A	G	20	GENIC	homozygous	51598957
10	109253473	109253474	C	T	27	GENIC	homozygous	51598958
10	109253550	109253551	C	T	31	GENIC	homozygous	51598959
10	109253913	109253914	G	A	27	GENIC	homozygous	51598960
10	109254408	109254409	T	A	16	GENIC	homozygous	51598961
10	109254420	109254421	T	C	11	GENIC	homozygous	51598962
10	109254475	109254476	T	TC	3	GENIC	homozygous	51598963
10	109254490	109254491	A	AAAC	10	GENIC	possibly homozygous	52814473
10	109254497	109254499	GC	--	9	GENIC	homozygous	51598966
10	109255130	109255131	C	-	33	GENIC	homozygous	51598967
10	109255397	109255398	A	C	24	GENIC	homozygous	51598968