chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9418372	9418373	G	A	31	GENIC	homozygous	63356264
20	9418477	9418478	G	A	26	GENIC	homozygous	63356266
20	9419309	9419310	C	G	35	GENIC	homozygous	63356268
20	9419538	9419539	C	T	35	GENIC	homozygous	63356270
20	9419719	9419720	T	C	36	GENIC	homozygous	63356272
20	9420706	9420707	A	G	27	GENIC	homozygous	63356274
20	9420984	9420985	C	T	20	GENIC	homozygous	63356276
20	9421452	9421453	G	A	35	GENIC	homozygous	63356278
20	9422294	9422295	C	T	32	GENIC	homozygous	63356280
20	9422415	9422416	G	A	24	GENIC	possibly homozygous	63356282
20	9422475	9422476	G	T	35	GENIC	homozygous	63356284
20	9422582	9422583	G	T	26	GENIC	homozygous	63356286