chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	99092275	99092275		T	17	GENIC	possibly homozygous	131136043
13	99092853	99092853		CTT	69	GENIC	homozygous	131136044
13	99093282	99093283	C	T	58	GENIC	homozygous	114651306
13	99094116	99094116		C	54	GENIC	homozygous	131136045
13	99094934	99094934		TCT	41	GENIC	homozygous	131136046
13	99095012	99095013	A	G	54	GENIC	homozygous	118547983
13	99095017	99095018	A	T	54	GENIC	homozygous	118547984
13	99095019	99095020	A	T	54	GENIC	homozygous	118547985
13	99095173	99095174	C	T	46	GENIC	homozygous	114437294
13	99095176	99095177	C	T	49	GENIC	homozygous	114437296
13	99095190	99095191	G	C	52	GENIC	homozygous	114437298
13	99095265	99095266	G	A	49	GENIC	homozygous	114437300
13	99096167	99096168	A	G	55	GENIC	homozygous	118547986
13	99096319	99096319		A	43	GENIC	homozygous	131136047
13	99096402	99096402		AACTATGTACTTTAAAGAAAAGATGAATTTTT	32	GENIC	homozygous	131136048
13	99098327	99098328	A	C	29	GENIC	homozygous	118547988
13	99098366	99098367	A	G	40	GENIC	homozygous	126105640
13	99098811	99098812	G	A	53	GENIC	homozygous	114651308
13	99099693	99099694	A	G	59	GENIC	homozygous	118547989
13	99101301	99101302	A	C	25	GENIC	homozygous	114651310
13	99101682	99101682		TTGGA	57	GENIC	homozygous	131136050
13	99099735	99099736	T	C	61	GENIC	homozygous	131140618