chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41393603	41393604	G	A	11	GENIC	homozygous	116928627
10	41393616	41393617	C	T	15	GENIC	homozygous	116571510
10	41394023	41394024	A	T	6	GENIC	homozygous	116571512
10	41394970	41394971	C	T	20	GENIC	homozygous	116571514
10	41396202	41396203	G	A	19	GENIC	homozygous	116872525
10	41396939	41396940	A	G	22	GENIC	possibly homozygous	116571518
10	41397460	41397461	A	G	7	GENIC	homozygous	116571520
10	41397679	41397680	T	C	12	GENIC	homozygous	116571522
10	41398705	41398706	A	G	15	GENIC	homozygous	116872527
10	41400001	41400002	G	T	19	GENIC	homozygous	116571524
10	41400305	41400306	A	G	24	GENIC	homozygous	116571526
10	41402337	41402338	T	C	11	GENIC	homozygous	116571538
10	41402751	41402752	A	G	16	GENIC	homozygous	116571540
10	41402767	41402768	C	T	13	GENIC	homozygous	116571542
10	41402786	41402787	T	C	15	GENIC	homozygous	116571544
10	41403325	41403326	G	A	13	GENIC	homozygous	116571546
10	41403987	41403988	C	T	13	GENIC	homozygous	116571548
10	41404173	41404174	G	T	26	GENIC	homozygous	116571550
10	41404385	41404386	T	A	11	GENIC	homozygous	116571554
10	41404568	41404569	T	C	8	GENIC	heterozygous	116872529
10	41404699	41404700	C	T	21	GENIC	homozygous	116571556
10	41404967	41404968	T	C	24	GENIC	homozygous	116571558
10	41405525	41405526	G	C	17	GENIC	homozygous	116571560
10	41405861	41405862	C	G	20	GENIC	homozygous	116571562
10	41406034	41406035	G	A	11	GENIC	homozygous	116571564
10	41406347	41406348	A	C	24	GENIC	homozygous	116571566