chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	122951734	122951735	C	G	17	GENIC	homozygous	111691754
3	122952291	122952292	C	T	32	GENIC	homozygous	111691755
3	122953647	122953648	A	G	32	GENIC	homozygous	111691756
3	122953884	122953885	T	C	32	GENIC	homozygous	111691757
3	122954412	122954413	G	T	25	GENIC	homozygous	111691758
3	122954414	122954415	A	C	26	GENIC	homozygous	111691759
3	122955655	122955656	G	A	34	GENIC	homozygous	111691761
3	122955860	122955861	G	A	39	GENIC	possibly homozygous	111691762
3	122957114	122957115	C	T	34	GENIC	homozygous	111691763
3	122957999	122958000	G	A	11	GENIC	homozygous	111691764
3	122958697	122958698	A	C	22	GENIC	homozygous	111691765
3	122958771	122958772	T	C	24	GENIC	homozygous	111691766
3	122962268	122962269	G	A	13	GENIC	homozygous	111691768
3	122962737	122962738	A	C	29	GENIC	homozygous	111691769
3	122962959	122962960	A	C	26	GENIC	homozygous	111691770
3	122965992	122965993	C	T	13	GENIC	homozygous	111691771
3	122966923	122966924	G	A	34	GENIC	homozygous	111691772
3	122967867	122967868	T	C	27	GENIC	homozygous	111691773