chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86600184	86600185	C		23	GENIC	homozygous	128842068
10	86601304	86601305	T	G	21	GENIC	homozygous	116816589
10	86602054	86602055	A	C	21	GENIC	homozygous	116816591
10	86604676	86604678	GA		27	GENIC	homozygous	131902378
10	86604737	86604738	A	T	32	GENIC	homozygous	116816595
10	86605234	86605235	A	C	6	GENIC	homozygous	117328681
10	86605248	86605249	A	C	8	GENIC	homozygous	117328683
10	86605269	86605269		CCCTGT	8	GENIC	homozygous	131902379
10	86605282	86605283	C	A	8	GENIC	homozygous	131906253
10	86605288	86605289	T	C	8	GENIC	homozygous	131906254
10	86605291	86605297	CCCTGA		8	GENIC	homozygous	131902380
10	86605711	86605712	A	G	37	GENIC	homozygous	116816599
10	86607810	86607811	A	G	22	GENIC	homozygous	116816603
10	86607990	86607991	T	C	34	GENIC	homozygous	116816605
10	86608635	86608636	A	G	23	GENIC	heterozygous	118047314
10	86608620	86608621	C	T	24	GENIC	heterozygous	118047312
10	86608632	86608633	C	T	24	GENIC	heterozygous	118047313
10	86608673	86608674	C	T	20	GENIC	heterozygous	118005203
10	86608653	86608654	G	C	21	GENIC	heterozygous	118005200
10	86608664	86608665	G	C	20	GENIC	heterozygous	118005201
10	86608667	86608668	G	A	20	GENIC	heterozygous	118005202
10	86609793	86609798	GGATG		14	GENIC	homozygous	131902381
10	86609801	86609802	G	T	15	GENIC	homozygous	131906255
10	86610373	86610373		GATGGAT	16	GENIC	homozygous	131902382