chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	103721917	103721918	G	A	9	GENIC	homozygous	141038031
10	103888802	103888803	A		19	GENIC	heterozygous	403296712
10	103888802	103888803	A	T	19	GENIC	homozygous	403296713
10	103949170	103949171	T	A	14	GENIC	possibly homozygous	403296714
10	103949170	103949171	T		14	GENIC	heterozygous	403296715
10	104080708	104080709	C	T	8	GENIC	homozygous	138866001
10	104080709	104080710	T	C	8	GENIC	homozygous	138866002
10	104080715	104080716	A	C	7	GENIC	homozygous	138866003
10	104082667	104082668	C	T	20	GENIC	possibly homozygous	403296724
10	104082667	104082668	C		20	GENIC	heterozygous	403296725
10	104091213	104091214	C		16	GENIC	heterozygous	403296732
10	104091213	104091214	C	G	16	GENIC	homozygous	403296733
10	104091217	104091218	C		14	GENIC	heterozygous	403296734
10	104091217	104091218	C	G	14	GENIC	homozygous	403296735
10	104091223	104091224	C		12	GENIC	heterozygous	403296736
10	104091223	104091224	C	G	12	GENIC	homozygous	403296737
10	104091231	104091232	C	G	13	GENIC	homozygous	403296738
10	104091231	104091232	C		13	GENIC	heterozygous	403296739
10	104091237	104091238	C	G	12	GENIC	homozygous	403296740
10	104091237	104091238	C		12	GENIC	heterozygous	403296741
10	104091247	104091248	C	G	12	GENIC	homozygous	403296742
10	104091247	104091248	C		12	GENIC	heterozygous	403296743
10	104157022	104157023	C	T	2	GENIC	homozygous	140905252
10	103997150	103997152	AC		12	GENIC	heterozygous	147830843
10	104038128	104038134	CTCAGC		16	GENIC	homozygous	144857946