chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141614109	141614110	G	A	30	GENIC	homozygous	109327679
1	141614630	141614631	C	A	31	GENIC	homozygous	109327682
1	141614795	141614796	C	T	30	GENIC	homozygous	109327683
1	141614809	141614810	G	A	33	GENIC	homozygous	109327684
1	141614821	141614822	T	C	34	GENIC	homozygous	108937013
1	141615466	141615467	C	T	41	GENIC	homozygous	109327685
1	141615671	141615672	C	A	33	GENIC	homozygous	109327686
1	141616415	141616416	T	A	42	GENIC	homozygous	109327687
1	141616974	141616975	C	T	17	GENIC	homozygous	108937023
1	141618503	141618504	G	A	39	GENIC	homozygous	109327688
1	141621204	141621205	G	A	29	GENIC	homozygous	109327689
1	141622163	141622164	T	A	21	GENIC	homozygous	109327690
1	141622662	141622663	T	C	30	GENIC	homozygous	108937038
1	141622879	141622880	G	A	29	GENIC	homozygous	109327691
1	141623775	141623776	G	A	32	GENIC	homozygous	109327692
1	141624426	141624427	T	C	40	GENIC	homozygous	108937041
1	141630931	141630932	C	T	30	GENIC	homozygous	108261386
1	141633222	141633223	A	G	29	GENIC	homozygous	109327693
1	141654417	141654418	G	A	29	GENIC	homozygous	108261406