chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	41393440	41393441	T	A	28	GENIC	possibly homozygous	116571508
10	41393603	41393604	G	A	46	GENIC	homozygous	116928627
10	41393616	41393617	C	T	39	GENIC	homozygous	116571510
10	41401500	41401501	A	G	41	GENIC	homozygous	116571528
10	41401617	41401618	A	G	27	GENIC	homozygous	116571530
10	41401882	41401883	G	A	44	GENIC	homozygous	116571532
10	41402075	41402076	G	A	31	GENIC	homozygous	116571534
10	41402135	41402138	TAG		31	GENIC	homozygous	128810450
10	41402138	41402139	A	C	31	GENIC	homozygous	116571536
10	41402337	41402338	T	C	33	GENIC	homozygous	116571538
10	41402786	41402787	T	C	52	GENIC	homozygous	116571544
10	41403325	41403326	G	A	48	GENIC	homozygous	116571546
10	41404173	41404174	G	T	35	GENIC	homozygous	116571550
10	41404699	41404700	C	T	47	GENIC	homozygous	116571556
10	41404967	41404968	T	C	29	GENIC	homozygous	116571558
10	41405525	41405526	G	C	39	GENIC	homozygous	116571560
10	41406347	41406348	A	C	30	GENIC	homozygous	116571566
10	41405446	41405446		G	35	GENIC	homozygous	133227464
10	41403351	41403352	A	G	50	GENIC	homozygous	117005994
10	41403847	41403848	G	A	30	GENIC	homozygous	117005996
10	41404027	41404028	G	A	38	GENIC	homozygous	117005998
10	41405424	41405425	C	T	40	GENIC	homozygous	117006000