chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102320055	102320056	G	A	15	GENIC	homozygous	143470797
10	102330174	102330175	T	C	13	GENIC	homozygous	143470798
10	102330537	102330538	G	A	13	GENIC	homozygous	143470799
10	102330544	102330545	G	T	14	GENIC	homozygous	143470800
10	102330626	102330627	C	T	14	GENIC	homozygous	143470801
10	102332497	102332498	C	T	20	GENIC	homozygous	143470802
10	102332497	102332498	C		20	GENIC	heterozygous	404017541
10	102333283	102333284	A	T	19	GENIC	homozygous	143470803
10	102334487	102334488	T	G	26	GENIC	homozygous	143470804
10	102336400	102336401	T	G	23	GENIC	homozygous	143470805
10	102338497	102338498	A	G	23	GENIC	homozygous	143470806
10	102340194	102340195	C	A	20	GENIC	homozygous	143470807
10	102340243	102340244	A	T	16	GENIC	homozygous	143470808
10	102340244	102340245	T	C	16	GENIC	homozygous	143470809
10	102340254	102340255	C	T	17	GENIC	homozygous	143470810
10	102340332	102340333	C	T	13	GENIC	homozygous	143470811
10	102340898	102340899	A	G	22	GENIC	homozygous	143470812
10	102341115	102341116	C	T	9	GENIC	homozygous	143470813
10	102342183	102342184	T	C	21	GENIC	homozygous	143470814
10	102343907	102343908	C	T	15	GENIC	homozygous	143470815
10	102343995	102343996	G	A	13	GENIC	homozygous	143470816
10	102346476	102346477	C	T	17	GENIC	homozygous	143470817
10	102347301	102347302	A	G	27	GENIC	homozygous	143470818
10	102347670	102347670		CTC	21	GENIC	homozygous	143436947
10	102340297	102340297		C	13	GENIC	homozygous	143436944
10	102341073	102341077	CCTG		8	GENIC	homozygous	143436945
10	102344443	102344443		AG	16	GENIC	homozygous	143436946
10	102347989	102347990	G	T	27	GENIC	homozygous	143470819
10	102354672	102354673	C	T	15	GENIC	homozygous	143470820
10	102360767	102360768	T		18	GENIC	possibly homozygous	143436948
10	102363901	102363902	G	A	25	GENIC	homozygous	143470821
10	102365093	102365094	C	T	16	GENIC	homozygous	143470822