chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82171790	82171791	T	C	14	GENIC	homozygous	51516821
10	82173847	82173848	C	T	12	GENIC	homozygous	51516822
10	82174937	82174938	A	G	9	GENIC	homozygous	51516824
10	82175305	82175306	A	-	19	GENIC	homozygous	51516825
10	82175825	82175826	A	C	23	GENIC	homozygous	51516826
10	82179931	82179932	C	T	27	GENIC	homozygous	51516827
10	82180114	82180115	A	C	33	GENIC	homozygous	51516828
10	82182402	82182403	G	C	12	GENIC	homozygous	51516829
10	82182408	82182409	C	G	15	GENIC	heterozygous	51516830
10	82182423	82182424	G	GT	5	GENIC	homozygous	51516831
10	82182796	82182797	G	GA	14	GENIC	possibly homozygous	51516832
10	82184776	82184777	T	TCATAC	24	GENIC	homozygous	51516833
10	82185481	82185482	C	CA	28	GENIC	homozygous	51516834
10	82182797	82182798	A	-	14	GENIC	heterozygous	51991930