chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	121010384	121010385	G	C	24	GENIC	heterozygous	109130937
1	121010395	121010396	T	A	27	GENIC	heterozygous	108739729
1	121010412	121010413	C	T	26	GENIC	heterozygous	109322390
1	121010435	121010436	G	A	27	GENIC	heterozygous	108202134
1	121010446	121010447	C	T	28	GENIC	heterozygous	108202136
1	121010416	121010417	T	C	25	GENIC	heterozygous	108202132
1	121010423	121010424	G	T	29	GENIC	heterozygous	108202133
1	121010441	121010442	T	A	28	GENIC	heterozygous	108202135
1	121010474	121010475	G	A	23	GENIC	heterozygous	108739732
1	121010491	121010492	C	A	22	GENIC	heterozygous	108202137
1	121010497	121010498	C	A	22	GENIC	heterozygous	108202138
1	121010509	121010510	A	C	22	GENIC	heterozygous	108202139
1	121010517	121010518	T	G	22	GENIC	heterozygous	108739733
1	121011742	121011743	C	A	18	GENIC	homozygous	109322391
1	121013170	121013171	T	A	26	GENIC	heterozygous	109047521
1	121013280	121013281	A	G	17	GENIC	homozygous	109322392
1	121014293	121014294	T	A	35	GENIC	homozygous	109322393
1	121015379	121015380	A	G	25	GENIC	homozygous	109322394
1	121015636	121015637	A	G	11	GENIC	homozygous	108202141