chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51398407	51398408	G	A	15	GENIC	possibly homozygous	52973359
8	51398551	51398552	C	T	22	GENIC	homozygous	52973360
8	51400720	51400721	T	A	15	GENIC	possibly homozygous	52973362
8	51400959	51400960	T	C	7	GENIC	homozygous	52973363
8	51401407	51401408	A	G	18	GENIC	homozygous	52973364
8	51401432	51401433	T	C	15	GENIC	homozygous	52973365
8	51401787	51401788	A	AG	17	GENIC	possibly homozygous	52973366
8	51402397	51402398	A	-	1	GENIC	homozygous	52973367
8	51402668	51402669	A	T	13	GENIC	possibly homozygous	52973368
8	51403077	51403078	G	GTTCCTAAACTTTATT	3	GENIC	heterozygous	53363698
8	51404035	51404036	C	-	4	GENIC	heterozygous	53386505
8	51404195	51404196	T	G	11	GENIC	homozygous	52973371
8	51404218	51404219	G	A	8	GENIC	homozygous	52973372
8	51404644	51404645	G	A	17	GENIC	heterozygous	52973373
8	51404705	51404706	T	C	25	GENIC	possibly homozygous	52973374
8	51405073	51405075	TT	--	8	GENIC	homozygous	52973375
8	51405258	51405259	G	A	22	GENIC	homozygous	52973376
8	51405608	51405609	A	ATG	5	GENIC	homozygous	52973378