chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53106794	53106795	A	G	25	GENIC	homozygous	109756954
2	53106928	53106929	T	C	21	GENIC	homozygous	109756955
2	53107137	53107138	A	G	29	GENIC	homozygous	109756956
2	53107509	53107510	G	T	19	GENIC	homozygous	109756957
2	53107735	53107736	T	C	35	GENIC	homozygous	109756958
2	53107824	53107825	T	C	30	GENIC	homozygous	109756959
2	53108341	53108342	A	G	21	GENIC	homozygous	110526720
2	53108834	53108835	T	C	25	GENIC	homozygous	109756960
2	53110799	53110800	C	T	22	GENIC	homozygous	110526722
2	53111521	53111522	C	T	9	GENIC	homozygous	109756961
2	53112110	53112111	A	T	17	GENIC	homozygous	109756962
2	53112190	53112191	G	A	22	GENIC	possibly homozygous	110526724
2	53112660	53112661	G	A	19	GENIC	homozygous	109756963
2	53115650	53115651	C	T	15	GENIC	homozygous	109756964
2	53116196	53116197	A	G	18	GENIC	possibly homozygous	109756966