chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	168098342	168098350	TCCTTCCT	--------	16	GENIC	possibly homozygous	57774480
3	168098420	168098421	C	T	61	GENIC	possibly homozygous	57774481
3	168098747	168098748	G	A	47	GENIC	heterozygous	58522113
3	168098786	168098787	T	A	47	GENIC	possibly homozygous	57774482
3	168101124	168101125	G	A	34	GENIC	heterozygous	57774483
3	168101812	168101813	G	A	46	GENIC	possibly homozygous	57774484
3	168102099	168102100	C	T	52	GENIC	homozygous	57774485
3	168102173	168102177	TCAT	----	39	GENIC	homozygous	57774486
3	168102917	168102918	A	G	37	GENIC	homozygous	57774487
3	168104266	168104267	A	G	44	GENIC	possibly homozygous	57774488
3	168104790	168104791	A	T	52	GENIC	heterozygous	57774489
3	168104891	168104895	CCAT	----	38	GENIC	possibly homozygous	57774490
3	168105144	168105145	C	-	55	GENIC	homozygous	57774491
3	168105318	168105322	ATCT	----	58	GENIC	heterozygous	57774492
3	168105321	168105322	T	TATCC	43	GENIC	homozygous	57774493
3	168106158	168106159	A	G	17	GENIC	homozygous	57774494
3	168107145	168107146	T	A	52	GENIC	possibly homozygous	57774495
3	168107712	168107715	CCA	---	28	GENIC	heterozygous	57774496
3	168107716	168107717	C	-	29	GENIC	heterozygous	57774497
3	168110870	168110871	G	T	46	GENIC	homozygous	57774498