chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	106231088	106231089	T	C	63	GENIC	homozygous	136782883
3	106231514	106231515	G	C	74	GENIC	homozygous	136782885
3	106232970	106232971	C	G	53	GENIC	homozygous	141524557
3	106233310	106233311	T	C	48	GENIC	homozygous	136782888
3	106233450	106233451	A		31	GENIC	heterozygous	403072903
3	106233448	106233449	A	G	31	GENIC	heterozygous	403072902
3	106233450	106233451	A	G	31	GENIC	possibly homozygous	403072904
3	106233461	106233462	T		31	GENIC	possibly homozygous	403072905
3	106233461	106233462	T	G	31	GENIC	heterozygous	403072906
3	106234662	106234663	T	C	24	GENIC	homozygous	403072907
3	106234662	106234663	T	G	24	GENIC	heterozygous	403072908
3	106234662	106234663	T		24	GENIC	heterozygous	403072909
3	106236387	106236388	C	T	32	GENIC	homozygous	145422624
3	106240579	106240580	A		13	GENIC	homozygous	403072910
3	106240579	106240580	A	T	13	GENIC	heterozygous	403072911
3	106240628	106240629	T	C	13	GENIC	homozygous	136782898
3	106240631	106240632	T	C	13	GENIC	homozygous	136782899
3	106233575	106233576	T	C	51	GENIC	homozygous	147348101
3	106233446	106233447	A		31	GENIC	heterozygous	403072899
3	106233446	106233447	A	G	31	GENIC	heterozygous	403072900
3	106233448	106233449	A		31	GENIC	heterozygous	403072901
3	106242821	106242823	GA		65	GENIC	homozygous	141478461