chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82053838	82053839	C	T	12	GENIC	homozygous	51516469
10	82053839	82053840	C	G	13	GENIC	homozygous	51516470
10	82053840	82053841	C	A	13	GENIC	homozygous	52322202
10	82053842	82053843	C	T	12	GENIC	homozygous	51516471
10	82053843	82053844	C	T	11	GENIC	homozygous	51516472
10	82053845	82053846	C	T	11	GENIC	homozygous	51516473
10	82053846	82053847	C	G	11	GENIC	homozygous	51516474
10	82064694	82064696	CA	--	9	GENIC	heterozygous	52390696
10	82073860	82073861	T	-	12	INTERGENIC	heterozygous	52390700
10	82087938	82087939	A	G	8	INTERGENIC	possibly homozygous	51516577
10	82099378	82099379	A	C	19	GENIC	homozygous	51516594
10	82100621	82100622	C	CA	22	INTERGENIC	homozygous	51516601
10	82108869	82108870	C	CA	12	GENIC	heterozygous	51516618
10	82110458	82110462	ACAC	----	7	GENIC	heterozygous	52390710
10	82110460	82110462	AC	--	7	GENIC	heterozygous	52390712
10	82116609	82116611	AG	--	5	GENIC	heterozygous	52390714
10	82116790	82116791	G	-	9	GENIC	heterozygous	52390716
10	82108871	82108872	A	-	12	GENIC	heterozygous	52506274
10	82116788	82116791	GGG	---	9	GENIC	heterozygous	52506276