chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141434565	141434566	G	T	19	GENIC	homozygous	108260665
1	141435037	141435038	A	G	20	GENIC	homozygous	108936824
1	141435056	141435057	T	C	17	GENIC	homozygous	108936825
1	141436965	141436966	C	T	33	GENIC	homozygous	108260667
1	141437185	141437186	G	A	33	GENIC	homozygous	108936826
1	141437869	141437870	C	T	36	GENIC	homozygous	108936827
1	141439321	141439322	G	A	18	GENIC	homozygous	109327570
1	141439743	141439744	A	G	18	GENIC	homozygous	108936828
1	141439881	141439882	G	A	16	GENIC	homozygous	108936829
1	141440026	141440027	T	C	19	GENIC	homozygous	108936830
1	141440771	141440772	C	T	16	GENIC	homozygous	108936831
1	141440963	141440964	C	T	18	GENIC	homozygous	108936832
1	141441083	141441084	A	G	20	GENIC	homozygous	108936833
1	141441834	141441835	T	C	23	GENIC	homozygous	108936835
1	141441858	141441859	T	A	18	GENIC	homozygous	108936836
1	141444612	141444613	C	T	21	GENIC	homozygous	108936839
1	141444667	141444668	G	A	23	GENIC	homozygous	108936840
1	141445107	141445108	A	G	16	GENIC	homozygous	108936841
1	141446953	141446954	A	G	14	GENIC	homozygous	108936842
1	141447513	141447514	C	T	37	GENIC	homozygous	108936843
1	141447726	141447727	C	T	40	GENIC	homozygous	108936844
1	141447906	141447907	A	G	43	GENIC	homozygous	108936845
1	141447997	141447998	G	A	21	GENIC	homozygous	108936846
1	141449657	141449658	G	T	10	GENIC	homozygous	108936852
1	141448002	141448003	T	G	21	GENIC	homozygous	108936847
1	141449015	141449016	G	A	19	GENIC	homozygous	108936850
1	141449575	141449576	C	T	23	GENIC	homozygous	108936851
1	141449659	141449660	G	T	10	GENIC	homozygous	108936853
1	141450278	141450279	A	T	34	GENIC	possibly homozygous	109327572
1	141451151	141451152	T	G	18	GENIC	homozygous	108936855
1	141451983	141451984	G	T	36	GENIC	homozygous	108260671