chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	209496435	209496436	C	T	10	GENIC	homozygous	109189738
1	209496479	209496480	C	T	13	GENIC	homozygous	109189740
1	209496532	209496533	C	T	8	GENIC	homozygous	109189742
1	209496533	209496534	A	G	8	GENIC	homozygous	109189744
1	209496568	209496569	A	G	14	GENIC	homozygous	109189746
1	209496588	209496589	T	A	8	GENIC	homozygous	109189747
1	209501396	209501397	G	A	10	GENIC	homozygous	125307918
1	209501710	209501711	G	A	21	GENIC	homozygous	125307919
1	209502511	209502512	C	T	7	GENIC	homozygous	125307920
1	209507327	209507328	G	A	12	GENIC	homozygous	125307923
1	209508906	209508907	A	G	7	GENIC	homozygous	125307925
1	209509050	209509051	T	C	8	GENIC	homozygous	125307926
1	209509489	209509490	G	A	9	GENIC	homozygous	125307927
1	209509539	209509540	A	G	22	GENIC	homozygous	125307928
1	209509637	209509638	G	C	9	GENIC	homozygous	125307929
1	209510073	209510074	A	G	7	GENIC	homozygous	125307930
1	209510977	209510978	C	T	16	GENIC	homozygous	125378070
1	209511009	209511010	T	C	19	GENIC	homozygous	125307932
1	209511455	209511456	A	G	16	GENIC	homozygous	125307933
1	209511480	209511481	C	T	8	GENIC	homozygous	125307934
1	209511554	209511555	C	T	14	GENIC	homozygous	125378071
1	209512042	209512043	T	C	9	GENIC	heterozygous	125378072
1	209512102	209512103	T	C	18	GENIC	homozygous	125307935
1	209512288	209512289	T	C	28	GENIC	homozygous	125307936