chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	80207977	80207978	A	G	23	GENIC	homozygous	138831420
10	80208290	80208291	G	T	22	GENIC	homozygous	138831421
10	80208561	80208562	A	G	17	GENIC	homozygous	138831422
10	80208835	80208836	A	G	20	GENIC	homozygous	138831423
10	80209086	80209087	C	G	16	GENIC	homozygous	138831424
10	80209888	80209889	T		12	GENIC	homozygous	138693364
10	80209941	80209941		CG	9	GENIC	possibly homozygous	138693365
10	80209987	80209988	A	C	8	GENIC	homozygous	138831425
10	80212931	80212932	T	C	17	GENIC	heterozygous	403733917
10	80212927	80212928	T		17	GENIC	homozygous	403733914
10	80212927	80212928	T	C	17	GENIC	heterozygous	403733915
10	80212929	80212930	T	C	17	GENIC	heterozygous	154647936
10	80212931	80212932	T		17	GENIC	homozygous	403733916
10	80212929	80212930	T		17	GENIC	homozygous	403637277
10	80212933	80212934	T	C	17	GENIC	heterozygous	154647937
10	80212933	80212934	T		17	GENIC	homozygous	403637278
10	80212935	80212936	T		17	GENIC	homozygous	403733918
10	80212935	80212936	T	C	17	GENIC	heterozygous	403733919
10	80212937	80212938	T		17	GENIC	homozygous	403637279
10	80212937	80212938	T	C	17	GENIC	heterozygous	403637280
10	80212941	80212942	T		17	GENIC	homozygous	403637281
10	80212941	80212942	T	C	17	GENIC	heterozygous	403637282
10	80212943	80212944	T		17	GENIC	homozygous	403637283
10	80212943	80212944	T	C	17	GENIC	heterozygous	403637284
10	80212945	80212946	T		17	GENIC	homozygous	403637285
10	80212945	80212946	T	C	17	GENIC	heterozygous	403637286
10	80213703	80213704	C	T	19	GENIC	homozygous	138831426
10	80214163	80214164	C	T	14	GENIC	homozygous	138831427