chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110304427	110304428	A	G	16	GENIC	homozygous	111672649
3	110304693	110304694	C	T	8	GENIC	possibly homozygous	111672651
3	110305015	110305016	A	T	5	GENIC	homozygous	119702344
3	110306725	110306726	A	G	16	GENIC	possibly homozygous	111672652
3	110307794	110307795	T	A	13	GENIC	homozygous	111672654
3	110308975	110308976	A	G	9	GENIC	homozygous	111672660
3	110310946	110310947	G	C	13	GENIC	homozygous	111672661
3	110311445	110311446	A	T	20	GENIC	homozygous	111672663
3	110312754	110312755	G	A	16	GENIC	homozygous	111672667
3	110314044	110314045	C	T	30	GENIC	homozygous	111672670
3	110314183	110314184	T	C	13	GENIC	homozygous	112138823
3	110315945	110315946	A	G	22	GENIC	homozygous	112138824
3	110317183	110317184	A	G	13	GENIC	homozygous	111672674
3	110317206	110317207	T	G	12	GENIC	homozygous	111672676
3	110317230	110317231	G	A	13	GENIC	homozygous	111672678
3	110317784	110317785	C	T	29	GENIC	homozygous	111672684
3	110317964	110317965	G	C	26	GENIC	homozygous	111672686
3	110318079	110318080	C	T	20	GENIC	homozygous	111672688
3	110320626	110320627	G	A	19	GENIC	homozygous	111672690
3	110320719	110320720	T	G	20	GENIC	homozygous	111672691
3	110323285	110323286	C	T	15	GENIC	homozygous	112138826
3	110323714	110323715	T	G	12	GENIC	homozygous	111672693
3	110323869	110323870	C	T	8	GENIC	homozygous	112292161