chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102320055	102320056	G	A	24	GENIC	homozygous	143470797
10	102330174	102330175	T	C	34	GENIC	homozygous	143470798
10	102330537	102330538	G	A	32	GENIC	homozygous	143470799
10	102330544	102330545	G	T	29	GENIC	homozygous	143470800
10	102330626	102330627	C	T	13	GENIC	homozygous	143470801
10	102332497	102332498	C	T	35	GENIC	homozygous	143470802
10	102332497	102332498	C		35	GENIC	heterozygous	404017541
10	102333283	102333284	A	T	35	GENIC	homozygous	143470803
10	102334487	102334488	T	G	58	GENIC	homozygous	143470804
10	102336400	102336401	T	G	48	GENIC	homozygous	143470805
10	102338497	102338498	A	G	58	GENIC	homozygous	143470806
10	102340194	102340195	C	A	38	GENIC	homozygous	143470807
10	102340243	102340244	A	T	46	GENIC	homozygous	143470808
10	102340244	102340245	T	C	46	GENIC	homozygous	143470809
10	102340254	102340255	C	T	45	GENIC	homozygous	143470810
10	102340297	102340297		C	44	GENIC	homozygous	143436944
10	102340332	102340333	C	T	38	GENIC	homozygous	143470811
10	102340898	102340899	A	G	44	GENIC	homozygous	143470812
10	102341073	102341077	CCTG		21	GENIC	homozygous	143436945
10	102341115	102341116	C	T	21	GENIC	homozygous	143470813
10	102342183	102342184	T	C	58	GENIC	homozygous	143470814
10	102343907	102343908	C	T	36	GENIC	homozygous	143470815
10	102343995	102343996	G	A	26	GENIC	homozygous	143470816
10	102344443	102344443		AG	46	GENIC	homozygous	143436946
10	102346476	102346477	C	T	37	GENIC	homozygous	143470817
10	102347301	102347302	A	G	54	GENIC	homozygous	143470818
10	102347670	102347670		CTC	55	GENIC	homozygous	143436947
10	102347989	102347990	G	T	46	GENIC	homozygous	143470819
10	102354672	102354673	C	T	23	GENIC	homozygous	143470820
10	102360767	102360768	T		20	GENIC	homozygous	143436948
10	102363901	102363902	G	A	45	GENIC	homozygous	143470821
10	102365093	102365094	C	T	40	GENIC	homozygous	143470822