chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47127174	47127178	TCTG	----	29	GENIC	homozygous	49751035
13	47131193	47131197	GTGT	----	10	GENIC	homozygous	49751036
13	47132021	47132022	G	GGT	12	GENIC	possibly homozygous	49751037
13	47133276	47133277	C	G	40	GENIC	homozygous	49751040
13	47135289	47135290	G	A	49	GENIC	heterozygous	49751041
13	47135291	47135292	C	A	45	GENIC	heterozygous	49751042
13	47135305	47135306	G	A	49	GENIC	heterozygous	49944901
13	47136412	47136413	T	G	58	GENIC	possibly homozygous	49751043
13	47143364	47143365	A	AGT	43	GENIC	homozygous	49751044
13	47143469	47143470	A	T	59	GENIC	homozygous	49751045
13	47144903	47144905	TG	--	9	GENIC	possibly homozygous	49751046
13	47145289	47145290	G	GCA	9	GENIC	heterozygous	49751047
13	47145290	47145292	CA	--	9	GENIC	heterozygous	49751048
13	47146349	47146350	C	T	43	GENIC	homozygous	49751049
13	47148272	47148273	T	TACAC	6	GENIC	heterozygous	49751051
13	47148504	47148505	G	C	53	GENIC	homozygous	49751052
13	47148523	47148524	T	A	58	GENIC	homozygous	49751053
13	47148707	47148708	G	A	61	GENIC	homozygous	49751054
13	47148886	47148887	G	-	43	GENIC	homozygous	49751055
13	47149215	47149216	T	C	59	GENIC	possibly homozygous	49751056
13	47149231	47149232	G	A	56	GENIC	homozygous	49751057
13	47149659	47149660	A	G	40	GENIC	homozygous	49751058