chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41393440	41393441	T	A	21	GENIC	homozygous	116571508
10	41393603	41393604	G	A	21	GENIC	homozygous	116928627
10	41393616	41393617	C	T	23	GENIC	homozygous	116571510
10	41401500	41401501	A	G	38	GENIC	homozygous	116571528
10	41401617	41401618	A	G	27	GENIC	homozygous	116571530
10	41402337	41402338	T	C	22	GENIC	homozygous	116571538
10	41402786	41402787	T	C	17	GENIC	homozygous	116571544
10	41403325	41403326	G	A	13	GENIC	homozygous	116571546
10	41403351	41403352	A	G	14	GENIC	homozygous	117005994
10	41403847	41403848	G	A	17	GENIC	homozygous	117005996
10	41404027	41404028	G	A	26	GENIC	homozygous	117005998
10	41404173	41404174	G	T	26	GENIC	homozygous	116571550
10	41404568	41404569	T	C	15	GENIC	homozygous	116872529
10	41404699	41404700	C	T	20	GENIC	homozygous	116571556
10	41404967	41404968	T	C	20	GENIC	homozygous	116571558
10	41405424	41405425	C	T	15	GENIC	homozygous	117006000
10	41405525	41405526	G	C	22	GENIC	homozygous	116571560
10	41406347	41406348	A	C	9	GENIC	homozygous	116571566