chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62472548	62472549	A	AAAAG	16	GENIC	possibly homozygous	53646692
8	62472597	62472598	G	A	16	GENIC	homozygous	53274212
8	62476372	62476373	T	-	16	GENIC	possibly homozygous	52669007
8	62476550	62476551	T	A	21	GENIC	homozygous	52991159
8	62476989	62476990	G	GGT	13	GENIC	heterozygous	52991160
8	62476989	62476990	G	GGTGT	13	GENIC	heterozygous	52991161
8	62478916	62478917	T	-	13	GENIC	homozygous	53182211
8	62479698	62479699	T	G	28	GENIC	homozygous	52991164
8	62480536	62480537	G	T	17	GENIC	homozygous	52991165
8	62480564	62480565	G	GAA	16	GENIC	heterozygous	52991166
8	62480564	62480565	G	GA	16	GENIC	possibly homozygous	53389496
8	62482591	62482592	G	GA	29	GENIC	homozygous	52669009
8	62482597	62482598	A	AG	28	GENIC	homozygous	52669011
8	62482600	62482601	A	G	26	GENIC	homozygous	53389497
8	62482602	62482603	A	G	26	GENIC	homozygous	52991168
8	62482606	62482607	C	CG	26	GENIC	homozygous	52669013
8	62482622	62482623	G	C	21	GENIC	homozygous	52669015
8	62482633	62482634	T	C	18	GENIC	homozygous	52669017
8	62482639	62482640	G	C	21	GENIC	homozygous	52669019
8	62482645	62482646	T	TG	23	GENIC	homozygous	52669021
8	62482651	62482652	G	A	25	GENIC	homozygous	52669023
8	62482656	62482657	A	G	25	GENIC	homozygous	52669025
8	62482659	62482660	G	-	29	GENIC	homozygous	52669027
8	62483302	62483303	A	AGTGTGTGTGT	7	GENIC	homozygous	53364095
8	62477604	62477605	T	-	27	GENIC	possibly homozygous	53701048
8	62479631	62479632	A	G	35	GENIC	homozygous	53300579
8	62480570	62480571	G	A	18	GENIC	homozygous	53300580
8	62482664	62482665	C	T	27	GENIC	homozygous	53364093
8	62482665	62482666	T	C	27	GENIC	homozygous	53364094
8	62483688	62483689	A	-	19	GENIC	homozygous	52991170
8	62483908	62483909	A	C	13	GENIC	homozygous	53701049
8	62486861	62486862	A	-	9	GENIC	possibly homozygous	52991176
8	62487979	62487980	G	C	26	GENIC	homozygous	52991177
8	62488695	62488696	G	A	32	GENIC	homozygous	53701050
8	62487301	62487303	TG	--	9	GENIC	homozygous	53605198