chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106495185	106495186	G	A	31	GENIC	homozygous	52407326
10	106495556	106495557	T	TCTCAATTTCTGC	31	GENIC	homozygous	51765779
10	106497138	106497139	T	C	25	GENIC	homozygous	52407328
10	106497212	106497213	C	CTTTTT	5	GENIC	homozygous	52407330
10	106497798	106497799	T	C	20	GENIC	homozygous	51765819
10	106498120	106498124	TGTC	----	14	GENIC	possibly homozygous	52407332
10	106498608	106498609	T	C	11	GENIC	homozygous	52407334
10	106498614	106498615	C	T	11	GENIC	homozygous	52407336
10	106498810	106498811	C	T	24	GENIC	homozygous	52407338
10	106498875	106498876	G	A	40	GENIC	homozygous	51765835
10	106499991	106499992	G	T	25	GENIC	homozygous	52407340
10	106500272	106500273	C	T	41	GENIC	homozygous	52407342
10	106500273	106500274	C	T	42	GENIC	homozygous	52407344
10	106500625	106500626	C	CT	9	GENIC	possibly homozygous	52407346
10	106500778	106500779	C	CTT	8	GENIC	homozygous	52407347
10	106500836	106500840	TTTA	----	7	GENIC	homozygous	52407349
10	106501026	106501027	T	-	8	GENIC	homozygous	51765872
10	106501354	106501355	G	A	27	GENIC	homozygous	52407351
10	106501407	106501408	C	CT	16	GENIC	possibly homozygous	52407352
10	106502188	106502189	C	T	45	GENIC	homozygous	51765888
10	106502641	106502642	C	T	37	GENIC	homozygous	52407354
10	106502820	106502821	A	G	27	GENIC	homozygous	51765900
10	106502967	106502968	G	C	25	GENIC	homozygous	52407355
10	106503027	106503028	T	C	25	GENIC	homozygous	51765901