chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14078321	14078322	T	C	55	GENIC	homozygous	142218460
10	14079875	14079876	G	A	44	GENIC	homozygous	142218461
10	14081563	14081564	C	T	45	GENIC	homozygous	142218462
10	14082066	14082067	A	G	55	GENIC	homozygous	142218463
10	14082158	14082159	A	T	51	GENIC	homozygous	142218464
10	14082352	14082353	T	C	54	GENIC	homozygous	142218465
10	14082818	14082831	GGTTCGGTCCCCA		29	GENIC	homozygous	142196907
10	14082904	14082908	AACA		38	GENIC	homozygous	142196908
10	14084033	14084034	T	C	59	GENIC	homozygous	138725967
10	14084854	14084855	T	G	23	GENIC	homozygous	142218466
10	14085082	14085083	G		63	GENIC	homozygous	142196909
10	14085964	14085965	C	T	43	GENIC	homozygous	142218467
10	14086285	14086286	A	G	51	GENIC	homozygous	142218468
10	14087935	14087936	C	T	45	GENIC	homozygous	142218469
10	14088089	14088090	A	G	56	GENIC	homozygous	142218470
10	14090832	14090833	A	G	50	GENIC	homozygous	142218471
10	14090856	14090857	A	C	58	GENIC	homozygous	142218472
10	14091852	14091857	TGGTT		29	GENIC	possibly homozygous	142196910
10	14093881	14093882	T	G	48	GENIC	homozygous	142218473
10	14094352	14094353	A	C	47	GENIC	homozygous	142218474
10	14100523	14100524	C	T	68	GENIC	homozygous	142218475
10	14103380	14103382	AA		53	GENIC	homozygous	142196911
10	14103652	14103653	T	C	64	GENIC	homozygous	142218476
10	14104112	14104113	T	C	48	GENIC	homozygous	142218477