chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141434565	141434566	G	T	30	GENIC	homozygous	108260665
1	141435037	141435038	A	G	24	GENIC	homozygous	108936824
1	141435056	141435057	T	C	28	GENIC	homozygous	108936825
1	141436965	141436966	C	T	23	GENIC	homozygous	108260667
1	141437185	141437186	G	A	31	GENIC	homozygous	108936826
1	141437869	141437870	C	T	35	GENIC	homozygous	108936827
1	141439321	141439322	G	A	24	GENIC	possibly homozygous	109327570
1	141439743	141439744	A	G	26	GENIC	possibly homozygous	108936828
1	141439881	141439882	G	A	26	GENIC	possibly homozygous	108936829
1	141440026	141440027	T	C	14	GENIC	homozygous	108936830
1	141440771	141440772	C	T	15	GENIC	homozygous	108936831
1	141440963	141440964	C	T	21	GENIC	possibly homozygous	108936832
1	141441083	141441084	A	G	16	GENIC	possibly homozygous	108936833
1	141441834	141441835	T	C	27	GENIC	homozygous	108936835
1	141441858	141441859	T	A	25	GENIC	homozygous	108936836
1	141444612	141444613	C	T	15	GENIC	possibly homozygous	108936839
1	141444667	141444668	G	A	19	GENIC	possibly homozygous	108936840
1	141445107	141445108	A	G	24	GENIC	possibly homozygous	108936841
1	141446575	141446576	C	T	14	GENIC	possibly homozygous	109327571
1	141446953	141446954	A	G	14	GENIC	homozygous	108936842
1	141447513	141447514	C	T	31	GENIC	possibly homozygous	108936843
1	141447726	141447727	C	T	32	GENIC	possibly homozygous	108936844
1	141447906	141447907	A	G	29	GENIC	possibly homozygous	108936845
1	141449015	141449016	G	A	16	GENIC	homozygous	108936850
1	141449575	141449576	C	T	30	GENIC	homozygous	108936851
1	141449657	141449658	G	T	31	GENIC	possibly homozygous	108936852
1	141449659	141449660	G	T	31	GENIC	possibly homozygous	108936853
1	141449674	141449675	C	A	33	GENIC	possibly homozygous	108936854
1	141450278	141450279	A	T	24	GENIC	homozygous	109327572
1	141451151	141451152	T	G	14	GENIC	homozygous	108936855
1	141451983	141451984	G	T	39	GENIC	homozygous	108260671