chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	8628348	8628349	C	T	63	GENIC	homozygous	111873061
3	8628574	8628575	T	C	81	GENIC	homozygous	111441976
3	8630186	8630187	A	T	63	GENIC	possibly homozygous	111873063
3	8630406	8630407	G	T	53	GENIC	possibly homozygous	111873065
3	8630634	8630635	G	C	57	GENIC	possibly homozygous	111873067
3	8634494	8634495	C	T	76	GENIC	homozygous	111873069
3	8636271	8636272	T	C	68	GENIC	homozygous	111441978
3	8639335	8639336	G	A	64	GENIC	homozygous	111873071
3	8639517	8639518	C	T	69	GENIC	homozygous	111873073
3	8639816	8639816		TTC	59	GENIC	homozygous	132038365
3	8640641	8640641		TG	62	GENIC	homozygous	132038366
3	8641722	8641722		CTT	77	GENIC	homozygous	131325016
3	8643092	8643093	A	G	53	GENIC	homozygous	111441982
3	8644708	8644709	T	G	70	GENIC	homozygous	111873075
3	8633061	8633061		C	17	GENIC	homozygous	127847957
3	8637940	8637941	A		47	GENIC	possibly homozygous	127847958
3	8645858	8645859	C	T	73	GENIC	homozygous	111873077
3	8647843	8647844	C	A	71	GENIC	possibly homozygous	111873079
3	8647933	8647934	T	C	77	GENIC	homozygous	111441983
3	8648439	8648440	G	A	73	GENIC	homozygous	111873081
3	8649053	8649054	A	G	46	GENIC	homozygous	111873083
3	8649121	8649122	C	A	34	GENIC	homozygous	111873085
3	8649238	8649248	TGTGTGTGTC		24	GENIC	homozygous	132038367
3	8649322	8649322		TGTC	31	GENIC	possibly homozygous	131325018
3	8650209	8650210	A	G	83	GENIC	homozygous	111873087
3	8651076	8651077	C		31	GENIC	homozygous	132038368
3	8651201	8651202	A	G	50	GENIC	homozygous	111873089
3	8651868	8651868		TT	41	GENIC	homozygous	132038369
3	8652632	8652635	TTC		73	GENIC	homozygous	132038370
3	8651078	8651079	A	G	33	GENIC	homozygous	132045865
3	8652393	8652394	A	G	76	GENIC	homozygous	111873091
3	8652466	8652467	A	G	70	GENIC	homozygous	111873093
3	8653020	8653021	A	T	86	GENIC	homozygous	111873095
3	8654535	8654536	A	G	59	GENIC	homozygous	111441988
3	8656321	8656322	T	C	83	GENIC	homozygous	111441990