chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86600184	86600185	C		42	GENIC	homozygous	128842068
10	86601304	86601305	T	G	49	GENIC	possibly homozygous	116816589
10	86602054	86602055	A	C	48	GENIC	possibly homozygous	116816591
10	86604676	86604678	GA		59	GENIC	homozygous	131902378
10	86604737	86604738	A	T	51	GENIC	homozygous	116816595
10	86605234	86605235	A	C	12	GENIC	homozygous	117328681
10	86605248	86605249	A	C	13	GENIC	homozygous	117328683
10	86605269	86605269		CCCTGT	13	GENIC	homozygous	131902379
10	86605282	86605283	C	A	13	GENIC	homozygous	131906253
10	86605288	86605289	T	C	13	GENIC	homozygous	131906254
10	86605291	86605297	CCCTGA		13	GENIC	homozygous	131902380
10	86605711	86605712	A	G	54	GENIC	homozygous	116816599
10	86607810	86607811	A	G	39	GENIC	homozygous	116816603
10	86607990	86607991	T	C	52	GENIC	homozygous	116816605
10	86609793	86609798	GGATG		15	GENIC	homozygous	131902381
10	86609801	86609802	G	T	16	GENIC	homozygous	131906255
10	86610373	86610373		GATGGAT	21	GENIC	possibly homozygous	131902382