chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86202713	86202714	C	T	45	GENIC	homozygous	144416437
10	86203643	86203643		C	24	GENIC	homozygous	138696983
10	86204239	86204245	GAGGGA		41	GENIC	homozygous	144412380
10	86204985	86204986	T	C	50	GENIC	possibly homozygous	144416438
10	86205194	86205195	C		42	GENIC	homozygous	138696984
10	86205683	86205684	A	G	66	GENIC	homozygous	144416439
10	86207529	86207530	C	G	38	GENIC	homozygous	144416440
10	86208239	86208240	C	T	53	GENIC	homozygous	144416441
10	86209969	86209969		TG	43	GENIC	homozygous	144412381
10	86210040	86210041	C		28	GENIC	homozygous	138696986
10	86210400	86210401	T	C	57	GENIC	homozygous	144416442
10	86210953	86210954	C	T	46	GENIC	homozygous	144416443
10	86215373	86215374	C	T	39	GENIC	homozygous	144416444
10	86216035	86216036	T	A	41	GENIC	homozygous	144416445
10	86216574	86216575	C	A	23	GENIC	homozygous	144416446
10	86216636	86216637	C		16	GENIC	homozygous	144412382
10	86217136	86217137	T	C	45	GENIC	homozygous	144416447
10	86218272	86218273	A	G	45	GENIC	homozygous	144416448
10	86206246	86206247	C		41	GENIC	possibly homozygous	403293736
10	86206246	86206247	C	A	41	GENIC	heterozygous	403293737