chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110304427	110304428	A	G	54	GENIC	possibly homozygous	111672649
3	110304693	110304694	C	T	44	GENIC	homozygous	111672651
3	110306725	110306726	A	G	58	GENIC	homozygous	111672652
3	110307794	110307795	T	A	40	GENIC	homozygous	111672654
3	110307945	110307946	C	A	34	GENIC	heterozygous	111672656
3	110308975	110308976	A	G	39	GENIC	homozygous	111672660
3	110310946	110310947	G	C	47	GENIC	homozygous	111672661
3	110311445	110311446	A	T	61	GENIC	homozygous	111672663
3	110312754	110312755	G	A	61	GENIC	homozygous	111672667
3	110312870	110312871	G	A	42	GENIC	possibly homozygous	111672668
3	110314044	110314045	C	T	52	GENIC	homozygous	111672670
3	110314630	110314631	G	A	77	GENIC	homozygous	111672672
3	110317183	110317184	A	G	14	GENIC	possibly homozygous	111672674
3	110317206	110317207	T	G	19	GENIC	possibly homozygous	111672676
3	110317230	110317231	G	A	28	GENIC	heterozygous	111672678
3	110317260	110317261	A	G	44	GENIC	heterozygous	111672680
3	110317784	110317785	C	T	47	GENIC	homozygous	111672684
3	110317964	110317965	G	C	74	GENIC	homozygous	111672686
3	110318079	110318080	C	T	72	GENIC	homozygous	111672688
3	110320626	110320627	G	A	49	GENIC	homozygous	111672690
3	110320719	110320720	T	G	52	GENIC	homozygous	111672691
3	110321573	110321574	T	C	62	GENIC	homozygous	112003537
3	110322755	110322756	T	C	70	GENIC	homozygous	112003539
3	110323403	110323404	A	T	19	GENIC	possibly homozygous	112003541
3	110323415	110323416	A	G	18	GENIC	possibly homozygous	112003543
3	110323433	110323434	A	G	11	GENIC	heterozygous	112003545
3	110323714	110323715	T	G	45	GENIC	homozygous	111672693
3	110323829	110323830	C	T	59	GENIC	possibly homozygous	112003547