chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	135465924	135465925	T	A	13	GENIC	homozygous	113386812
4	135466280	135466281	G	C	20	GENIC	possibly homozygous	113386814
4	135466418	135466419	A	C	23	GENIC	possibly homozygous	113386816
4	135466667	135466668	T	C	9	GENIC	possibly homozygous	113386818
4	135466772	135466773	G	T	23	GENIC	homozygous	113386820
4	135466907	135466908	T	C	22	GENIC	possibly homozygous	113386822
4	135467006	135467007	G	A	19	GENIC	possibly homozygous	113386824
4	135467071	135467072	A	G	17	GENIC	homozygous	113386826
4	135467321	135467322	T	G	15	GENIC	heterozygous	113386828
4	135467032	135467033	A	T	21	GENIC	homozygous	112837008
4	135468099	135468100	A	G	15	GENIC	possibly homozygous	113386830
4	135468125	135468126	T	C	24	GENIC	possibly homozygous	113386832
4	135468148	135468149	G	A	25	GENIC	possibly homozygous	113386834
4	135468362	135468363	G	C	18	GENIC	homozygous	113386836
4	135468511	135468512	T	G	23	GENIC	possibly homozygous	113386838
4	135469761	135469762	T	C	28	GENIC	homozygous	113386840
4	135469848	135469849	A	G	10	GENIC	homozygous	113386842
4	135469902	135469903	G	C	10	GENIC	homozygous	113386844
4	135469948	135469949	C	T	16	GENIC	homozygous	113386846
4	135470013	135470014	G	A	18	GENIC	homozygous	113386848