chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47127173	47127174	T	TTCTG	16	GENIC	heterozygous	50390582
13	47127174	47127178	TCTG	----	16	GENIC	possibly homozygous	49751035
13	47131193	47131197	GTGT	----	11	GENIC	homozygous	49751036
13	47132021	47132022	G	GGT	11	GENIC	homozygous	49751037
13	47133276	47133277	C	G	20	GENIC	homozygous	49751040
13	47135289	47135290	G	A	6	GENIC	heterozygous	49751041
13	47135291	47135292	C	A	5	GENIC	heterozygous	49751042
13	47136412	47136413	T	G	4	GENIC	homozygous	49751043
13	47143364	47143365	A	AGT	17	GENIC	homozygous	49751044
13	47143469	47143470	A	T	13	GENIC	possibly homozygous	49751045
13	47144903	47144905	TG	--	11	GENIC	homozygous	49751046
13	47145289	47145290	G	GCA	9	GENIC	heterozygous	49751047
13	47146349	47146350	C	T	17	GENIC	homozygous	49751049
13	47148024	47148025	T	TACACACAC	19	GENIC	heterozygous	50357804
13	47148272	47148273	T	TAC	12	GENIC	heterozygous	49751050
13	47148272	47148273	T	TACAC	12	GENIC	heterozygous	49751051
13	47148504	47148505	G	C	40	GENIC	homozygous	49751052
13	47148523	47148524	T	A	39	GENIC	homozygous	49751053
13	47148707	47148708	G	A	30	GENIC	homozygous	49751054
13	47148886	47148887	G	-	12	GENIC	homozygous	49751055
13	47149215	47149216	T	C	21	GENIC	homozygous	49751056
13	47149231	47149232	G	A	22	GENIC	homozygous	49751057
13	47149659	47149660	A	G	18	GENIC	homozygous	49751058