chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	29082388	29082389	T	C	36	GENIC	homozygous	113001826
4	29082410	29082411	T	G	30	GENIC	homozygous	113001828
4	29083423	29083424	A	G	33	GENIC	possibly homozygous	113001830
4	29083892	29083893	G	A	15	GENIC	homozygous	113001832
4	29083969	29083970	A	C	29	GENIC	homozygous	113001834
4	29084163	29084164	T	C	25	GENIC	homozygous	113001836
4	29084208	29084209	G	C	21	GENIC	homozygous	113001838
4	29085426	29085427	T	C	17	GENIC	homozygous	113001840
4	29085919	29085920	C	T	30	GENIC	homozygous	113001842
4	29086948	29086949	T	C	26	GENIC	homozygous	113001858
4	29087518	29087519	T	C	31	GENIC	homozygous	113001860
4	29088661	29088662	C	A	23	GENIC	homozygous	113001862
4	29089386	29089387	T	C	29	GENIC	homozygous	113001864
4	29089608	29089609	G	T	18	GENIC	possibly homozygous	113001866
4	29090029	29090030	T	C	17	GENIC	heterozygous	113001868
4	29090602	29090603	T	A	26	GENIC	homozygous	113001872
4	29091315	29091316	G	A	24	GENIC	possibly homozygous	113001874
4	29091422	29091423	C	T	26	GENIC	possibly homozygous	113001876
4	29091458	29091459	A	G	29	GENIC	possibly homozygous	113001878