chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82053838	82053839	C	T	11	GENIC	homozygous	51516469
10	82053839	82053840	C	G	11	GENIC	homozygous	51516470
10	82053840	82053841	C	A	11	GENIC	homozygous	52322202
10	82053842	82053843	C	T	11	GENIC	homozygous	51516471
10	82053843	82053844	C	T	11	GENIC	homozygous	51516472
10	82053845	82053846	C	T	13	GENIC	homozygous	51516473
10	82053846	82053847	C	G	13	GENIC	homozygous	51516474
10	82064694	82064696	CA	--	8	GENIC	heterozygous	52390696
10	82073860	82073861	T	-	11	INTERGENIC	heterozygous	52390700
10	82087337	82087338	G	GT	9	INTERGENIC	heterozygous	52444006
10	82087339	82087340	T	-	9	INTERGENIC	heterozygous	52461985
10	82087938	82087939	A	G	9	INTERGENIC	possibly homozygous	51516577
10	82099378	82099379	A	C	15	GENIC	homozygous	51516594
10	82100621	82100622	C	CA	5	INTERGENIC	homozygous	51516601
10	82103815	82103817	GT	--	18	INTERGENIC	heterozygous	52461986
10	82108869	82108870	C	CA	10	GENIC	heterozygous	51516618
10	82110460	82110462	AC	--	4	GENIC	heterozygous	52390712
10	82108870	82108872	AA	--	10	GENIC	heterozygous	52650355
10	82108871	82108872	A	-	10	GENIC	heterozygous	52506274