chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88121187	88121188	G	A	14	GENIC	heterozygous	52205793
10	88121196	88121197	T	C	17	GENIC	homozygous	52205795
10	88121289	88121290	C	T	8	GENIC	homozygous	52205797
10	88121663	88121664	C	A	9	GENIC	possibly homozygous	52205799
10	88121676	88121677	G	A	10	GENIC	homozygous	52205801
10	88121834	88121835	C	CT	1	GENIC	homozygous	51924808
10	88122441	88122442	A	G	18	GENIC	heterozygous	52205807
10	88122707	88122711	TACA	----	7	GENIC	homozygous	52205809
10	88122754	88122755	C	CTTT	2	GENIC	homozygous	52205811
10	88122857	88122858	C	A	10	GENIC	possibly homozygous	52205813
10	88123107	88123108	A	G	23	GENIC	heterozygous	52205815
10	88123268	88123269	T	C	3	GENIC	homozygous	52205817
10	88123271	88123273	CA	--	1	GENIC	homozygous	52205819
10	88123347	88123348	T	C	7	GENIC	possibly homozygous	52205821
10	88123689	88123693	AGAA	----	8	GENIC	homozygous	52205835
10	88123812	88123813	T	C	11	GENIC	homozygous	52205837
10	88126403	88126404	T	C	10	GENIC	homozygous	52205839
10	88126420	88126423	TTG	---	3	GENIC	heterozygous	52393618
10	88126426	88126427	T	G	3	GENIC	heterozygous	52393620
10	88126515	88126516	A	G	7	GENIC	homozygous	52205845
10	88126926	88126927	C	G	2	GENIC	homozygous	52205851
10	88128019	88128020	A	T	4	GENIC	heterozygous	52205853
10	88130348	88130349	C	T	20	GENIC	possibly homozygous	52205857
10	88130546	88130547	C	T	27	GENIC	possibly homozygous	52205859
10	88130882	88130883	G	A	16	GENIC	homozygous	52205861