chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35644604	35644605	C	A	18	GENIC	homozygous	51408523
10	35644877	35644878	G	A	18	GENIC	homozygous	51408525
10	35645595	35645596	A	G	9	GENIC	homozygous	51408527
10	35645648	35645649	G	A	27	GENIC	possibly homozygous	51408529
10	35645753	35645754	C	CT	16	GENIC	homozygous	51408531
10	35646249	35646250	T	TA	23	GENIC	possibly homozygous	51408533
10	35646456	35646457	C	A	12	GENIC	homozygous	51408535
10	35646465	35646466	C	A	10	GENIC	homozygous	51408537
10	35646626	35646627	C	CT	4	GENIC	homozygous	51408539
10	35646862	35646863	C	CT	7	GENIC	heterozygous	51408541
10	35647810	35647811	C	T	11	GENIC	possibly homozygous	51408543
10	35647960	35647961	C	CATCA	7	GENIC	homozygous	51408545
10	35648059	35648060	A	C	18	GENIC	possibly homozygous	51408549
10	35648391	35648392	T	C	4	GENIC	homozygous	51408555
10	35648422	35648423	A	G	7	GENIC	homozygous	51408557
10	35649061	35649062	C	T	12	GENIC	homozygous	51408559
10	35649071	35649072	C	T	10	GENIC	homozygous	51408561
10	35649108	35649109	T	C	13	GENIC	heterozygous	51408563
10	35649202	35649203	C	A	15	GENIC	homozygous	51408565
10	35649915	35649916	G	GT	5	GENIC	heterozygous	51408567
10	35650183	35650184	C	CTT	3	GENIC	homozygous	51408569
10	35650199	35650200	C	CT	2	GENIC	homozygous	51408571
10	35650512	35650513	A	G	18	GENIC	possibly homozygous	51408575