chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157333509	157333510	C	T	27	GENIC	homozygous	126027691
4	157333552	157333553	C	T	12	GENIC	homozygous	126027692
4	157334536	157334537	T	C	15	GENIC	homozygous	126027693
4	157335019	157335020	C	A	14	GENIC	homozygous	126027694
4	157336302	157336303	T	C	25	GENIC	homozygous	126027695
4	157336622	157336623	A	C	20	GENIC	homozygous	126027696
4	157336830	157336831	C	T	15	GENIC	homozygous	126027697
4	157337844	157337845	G	A	13	GENIC	homozygous	126027698
4	157340118	157340119	G	A	13	GENIC	homozygous	126027699
4	157340128	157340129	A	C	18	GENIC	homozygous	126027700
4	157340656	157340657	T	C	11	GENIC	homozygous	126027701
4	157341749	157341750	T	C	13	GENIC	homozygous	113184496
4	157341839	157341840	T	C	18	GENIC	homozygous	112905917
4	157342669	157342670	A	G	25	GENIC	homozygous	112905921
4	157342693	157342694	A	G	15	GENIC	homozygous	112905923
4	157343043	157343044	C	T	22	GENIC	homozygous	112905925
4	157345115	157345116	T	C	15	GENIC	homozygous	112905929
4	157345228	157345229	G	T	18	GENIC	homozygous	112905931
4	157345309	157345310	T	C	25	GENIC	homozygous	112905933
4	157345444	157345445	T	G	20	GENIC	homozygous	112905935
4	157347302	157347303	C	T	6	GENIC	homozygous	113062866