chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62472534	62472535	C	CA	13	GENIC	heterozygous	52669006
8	62472535	62472537	AA	--	13	GENIC	heterozygous	53124709
8	62474490	62474491	C	T	19	GENIC	homozygous	52991157
8	62474494	62474495	C	T	19	GENIC	homozygous	52991158
8	62476550	62476551	T	A	21	GENIC	homozygous	52991159
8	62476989	62476990	G	GGT	11	GENIC	heterozygous	52991160
8	62476989	62476990	G	GGTGT	11	GENIC	heterozygous	52991161
8	62478915	62478916	A	AT	13	GENIC	heterozygous	52991162
8	62478915	62478916	A	ATT	13	GENIC	heterozygous	52991163
8	62479631	62479632	A	G	31	GENIC	homozygous	53300579
8	62479698	62479699	T	G	21	GENIC	homozygous	52991164
8	62480536	62480537	G	T	32	GENIC	homozygous	52991165
8	62480564	62480565	G	GAA	15	GENIC	possibly homozygous	52991166
8	62480570	62480571	G	A	28	GENIC	homozygous	53300580
8	62482591	62482592	G	GA	9	GENIC	homozygous	52669009
8	62482597	62482598	A	AG	9	GENIC	homozygous	52669011
8	62482602	62482603	A	G	8	GENIC	homozygous	52991168
8	62482606	62482607	C	CG	9	GENIC	homozygous	52669013
8	62482622	62482623	G	C	8	GENIC	homozygous	52669015
8	62482633	62482634	T	C	10	GENIC	homozygous	52669017
8	62482639	62482640	G	C	10	GENIC	homozygous	52669019
8	62482645	62482646	T	TG	8	GENIC	homozygous	52669021
8	62482651	62482652	G	A	9	GENIC	homozygous	52669023
8	62482656	62482657	A	G	9	GENIC	homozygous	52669025
8	62482659	62482660	G	-	9	GENIC	homozygous	52669027
8	62483033	62483037	TCAG	----	25	GENIC	homozygous	52991169
8	62483688	62483689	A	-	6	GENIC	homozygous	52991170
8	62483808	62483813	AAAAA	-----	10	GENIC	heterozygous	52991172
8	62483827	62483828	T	G	16	GENIC	heterozygous	52669029
8	62485822	62485823	C	T	8	GENIC	homozygous	52991174
8	62486439	62486440	T	G	28	GENIC	homozygous	53300581
8	62486859	62486862	AAA	---	13	GENIC	heterozygous	53274219
8	62486860	62486862	AA	--	13	GENIC	heterozygous	52991175
8	62487979	62487980	G	C	12	GENIC	homozygous	52991177
8	62489496	62489497	G	A	25	GENIC	homozygous	53300582
8	62490541	62490542	A	G	21	GENIC	homozygous	52991179