chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	64326894	64326897	AGA		49	GENIC	possibly homozygous	133190167
8	64327272	64327273	G	C	52	GENIC	homozygous	117944588
8	64327278	64327279	A	T	53	GENIC	homozygous	122982762
8	64327347	64327349	TG		57	GENIC	possibly homozygous	133190168
8	64327350	64327350		AT	62	GENIC	possibly homozygous	133190169
8	64327368	64327369	G	C	58	GENIC	heterozygous	133201481
8	64327329	64327330	C	A	52	GENIC	homozygous	133201478
8	64327337	64327338	C	T	52	GENIC	heterozygous	133201479
8	64327344	64327345	T	C	55	GENIC	homozygous	133201480
8	64327388	64327389	A	C	53	GENIC	heterozygous	122982764
8	64327389	64327390	G	A	53	GENIC	heterozygous	122982765
8	64327394	64327395	G	T	52	GENIC	heterozygous	133201482
8	64327426	64327427	G	A	47	GENIC	homozygous	116840858
8	64327439	64327440	A	C	50	GENIC	heterozygous	133201483
8	64327464	64327465	C	T	55	GENIC	heterozygous	133201484
8	64327475	64327476	T	C	53	GENIC	heterozygous	133201485
8	64327484	64327485	C	G	51	GENIC	heterozygous	133201486
8	64327575	64327576	C	G	55	GENIC	homozygous	133201487
8	64327596	64327597	C	T	47	GENIC	homozygous	133201488
8	64327616	64327617	G	A	45	GENIC	homozygous	116840860
8	64327622	64327623	C	T	46	GENIC	homozygous	116840862
8	64327623	64327624	C	G	47	GENIC	homozygous	116840864
8	64327817	64327818	T	C	48	GENIC	homozygous	117944589
8	64330886	64330887	A	G	42	GENIC	homozygous	116840872
8	64332222	64332223	C	T	37	GENIC	homozygous	117944590
8	64332296	64332297	G		50	GENIC	homozygous	130364049
8	64327642	64327642		ACACTA	47	GENIC	homozygous	130364047
8	64334873	64334874	C	T	42	GENIC	homozygous	116840878
8	64334905	64334906	G	A	48	GENIC	homozygous	117944591
8	64337881	64337882	T	C	53	GENIC	homozygous	116840882
8	64340406	64340407	G	C	54	GENIC	homozygous	116840886
8	64344661	64344662	G	A	58	GENIC	homozygous	116840895
8	64345827	64345828	C	T	47	GENIC	homozygous	117944592
8	64350039	64350040	G	T	47	GENIC	homozygous	116840907