chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141439321	141439322	G	A	21	GENIC	homozygous	109327570
1	141439743	141439744	A	G	11	GENIC	homozygous	108936828
1	141440771	141440772	C	T	5	GENIC	homozygous	108936831
1	141440963	141440964	C	T	12	GENIC	homozygous	108936832
1	141441834	141441835	T	C	11	GENIC	homozygous	108936835
1	141441858	141441859	T	A	7	GENIC	homozygous	108936836
1	141444612	141444613	C	T	12	GENIC	homozygous	108936839
1	141444667	141444668	G	A	9	GENIC	homozygous	108936840
1	141445107	141445108	A	G	7	GENIC	homozygous	108936841
1	141447513	141447514	C	T	19	GENIC	homozygous	108936843
1	141447726	141447727	C	T	17	GENIC	homozygous	108936844
1	141447906	141447907	A	G	10	GENIC	homozygous	108936845
1	141448281	141448282	T	C	13	GENIC	homozygous	108936849
1	141449015	141449016	G	A	10	GENIC	homozygous	108936850
1	141449575	141449576	C	T	19	GENIC	homozygous	108936851
1	141449657	141449658	G	T	6	GENIC	heterozygous	108936852
1	141449659	141449660	G	T	6	GENIC	heterozygous	108936853
1	141449674	141449675	C	A	7	GENIC	homozygous	108936854
1	141450278	141450279	A	T	15	GENIC	homozygous	109327572
1	141451983	141451984	G	T	17	GENIC	homozygous	108260671
1	141448716	141448717	A	C	8	GENIC	heterozygous	125369076