chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106719900	106719901	G	A	39	GENIC	homozygous	403297299
10	106719900	106719901	G		39	GENIC	heterozygous	403297300
10	106722574	106722575	T		42	GENIC	homozygous	138703833
10	106722207	106722207		G	50	GENIC	homozygous	138703830
10	106722560	106722560		T	43	GENIC	homozygous	138703831
10	106722566	106722567	T		43	GENIC	homozygous	138703832
10	106725165	106725165		T	40	GENIC	homozygous	138703834
10	106721624	106721625	T	C	42	GENIC	homozygous	138869447
10	106722558	106722559	T	C	43	GENIC	homozygous	138869448
10	106725191	106725191		T	38	GENIC	homozygous	138703835
10	106735226	106735227	C		65	GENIC	homozygous	138703836
10	106769003	106769004	C		7	GENIC	homozygous	403297319
10	106769003	106769004	C	T	7	GENIC	heterozygous	403297320
10	106789733	106789734	G		17	GENIC	heterozygous	403297327
10	106789733	106789734	G	A	17	GENIC	heterozygous	403297328
10	106800048	106800049	T		19	GENIC	heterozygous	403297331
10	106800048	106800049	T	C	19	GENIC	heterozygous	403297332
10	106828508	106828508		A	43	GENIC	possibly homozygous	138703837
10	106836781	106836781		G	55	GENIC	homozygous	138703838
10	106836894	106836894		G	44	GENIC	homozygous	138703839
10	106839814	106839815	A		74	GENIC	homozygous	138703840
10	106842568	106842569	T		48	GENIC	homozygous	138703841
10	106842580	106842580		G	52	GENIC	homozygous	138703842
10	106843189	106843190	G		54	GENIC	homozygous	138703843
10	106843254	106843254		C	46	GENIC	homozygous	138703844
10	106852316	106852316		A	51	GENIC	homozygous	138703845
10	106852396	106852397	T		47	GENIC	homozygous	138703846
10	106852893	106852894	T		14	GENIC	homozygous	138703847