chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35644604	35644605	C	A	44	GENIC	homozygous	51408523
10	35644877	35644878	G	A	42	GENIC	homozygous	51408525
10	35645595	35645596	A	G	34	GENIC	homozygous	51408527
10	35645648	35645649	G	A	26	GENIC	homozygous	51408529
10	35645753	35645754	C	CT	29	GENIC	homozygous	51408531
10	35646249	35646250	T	TA	26	GENIC	homozygous	51408533
10	35646456	35646457	C	A	27	GENIC	homozygous	51408535
10	35646465	35646466	C	A	26	GENIC	homozygous	51408537
10	35646626	35646627	C	CT	20	GENIC	homozygous	51408539
10	35646862	35646863	C	CT	27	GENIC	possibly homozygous	51408541
10	35647810	35647811	C	T	48	GENIC	homozygous	51408543
10	35647960	35647961	C	CATCA	38	GENIC	homozygous	51408545
10	35648059	35648060	A	C	32	GENIC	homozygous	51408549
10	35648144	35648147	TTA	---	45	GENIC	homozygous	51408551
10	35648149	35648150	A	-	42	GENIC	homozygous	51408553
10	35648364	35648368	CAAA	----	24	GENIC	possibly homozygous	52435365
10	35648368	35648369	C	CGTTT	23	GENIC	possibly homozygous	52435367
10	35648391	35648392	T	C	26	GENIC	homozygous	51408555
10	35648422	35648423	A	G	29	GENIC	homozygous	51408557
10	35649061	35649062	C	T	43	GENIC	homozygous	51408559
10	35649071	35649072	C	T	41	GENIC	homozygous	51408561
10	35649108	35649109	T	C	41	GENIC	homozygous	51408563
10	35649202	35649203	C	A	43	GENIC	homozygous	51408565
10	35649915	35649916	G	GT	32	GENIC	possibly homozygous	51408567
10	35650183	35650184	C	CTT	33	GENIC	homozygous	51408569
10	35650199	35650200	C	CT	34	GENIC	homozygous	51408571
10	35650512	35650513	A	G	28	GENIC	homozygous	51408575