chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82053838	82053839	C	T	7	GENIC	homozygous	51516469
10	82053839	82053840	C	G	7	GENIC	homozygous	51516470
10	82053840	82053841	C	A	7	GENIC	homozygous	52322202
10	82053842	82053843	C	T	7	GENIC	homozygous	51516471
10	82053843	82053844	C	T	7	GENIC	homozygous	51516472
10	82053845	82053846	C	T	7	GENIC	homozygous	51516473
10	82053846	82053847	C	G	7	GENIC	homozygous	51516474
10	82056986	82056990	CTCT	----	10	GENIC	heterozygous	52444004
10	82064694	82064696	CA	--	3	GENIC	heterozygous	52390696
10	82068697	82068698	A	AGAGAGAG	12	GENIC	heterozygous	52390698
10	82087337	82087338	G	GT	14	INTERGENIC	heterozygous	52444006
10	82087938	82087939	A	G	9	INTERGENIC	possibly homozygous	51516577
10	82099378	82099379	A	C	15	GENIC	homozygous	51516594
10	82100621	82100622	C	CA	3	INTERGENIC	homozygous	51516601
10	82103815	82103817	GT	--	18	INTERGENIC	heterozygous	52461986
10	82106997	82106998	G	GAA	11	GENIC	heterozygous	51516611
10	82106997	82106998	G	GA	11	GENIC	heterozygous	51919839
10	82111384	82111385	C	-	6	GENIC	heterozygous	51516627
10	82116608	82116609	C	CAGAGAG	6	GENIC	heterozygous	53028258
10	82116609	82116611	AG	--	6	GENIC	heterozygous	52390714