chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	73316526	73316527	C	T	38	GENIC	heterozygous	52676503
8	73317698	73317699	A	AT	40	GENIC	homozygous	52676504
8	73317703	73317704	A	-	37	GENIC	homozygous	52676505
8	73324305	73324306	A	-	6	GENIC	heterozygous	52676506
8	73329845	73329846	A	AG	34	GENIC	homozygous	52676507
8	73338312	73338313	A	ATT	14	GENIC	heterozygous	52676508
8	73345020	73345021	C	T	49	GENIC	homozygous	52676509
8	73347486	73347493	TTGTCAT	-------	16	GENIC	heterozygous	52676510
8	73347498	73347499	G	GCATCA	15	GENIC	heterozygous	52676511
8	73350554	73350555	G	-	5	GENIC	homozygous	52676512
8	73350560	73350561	G	GC	9	GENIC	homozygous	52676513
8	73357913	73357914	T	-	26	GENIC	heterozygous	52676514
8	73362013	73362014	C	T	17	GENIC	heterozygous	52676515
8	73364663	73364664	T	TGAG	20	GENIC	homozygous	52676516
8	73365544	73365546	CT	--	20	GENIC	homozygous	52676517
8	73365549	73365550	T	-	20	GENIC	homozygous	52676518
8	73365553	73365554	T	-	19	GENIC	homozygous	52676519
8	73365558	73365559	T	-	15	GENIC	homozygous	52676520
8	73365561	73365564	TAT	---	15	GENIC	homozygous	52676521
8	73365569	73365570	T	-	15	GENIC	homozygous	52676522
8	73365574	73365575	T	-	27	GENIC	homozygous	52676523
8	73365587	73365588	T	-	28	GENIC	homozygous	52676524