chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5458677	5458678	C	T	28	GENIC	homozygous	109390297
20	5459469	5459470	G	A	22	GENIC	homozygous	109390298
20	5459525	5459526	G	A	15	GENIC	homozygous	109390299
20	5459584	5459585	A	C	26	GENIC	homozygous	109078066
20	5460329	5460330	G	A	33	GENIC	homozygous	109390300
20	5461226	5461227	T	C	25	GENIC	homozygous	109078074
20	5461370	5461371	T	G	29	GENIC	homozygous	109078076
20	5461632	5461633	C	T	23	GENIC	homozygous	109390301
20	5461924	5461925	T	C	29	GENIC	homozygous	109078078
20	5463884	5463885	G	A	18	GENIC	homozygous	109390302
20	5464192	5464193	A	G	20	GENIC	homozygous	109390303
20	5464254	5464255	T	A	26	GENIC	homozygous	109078080
20	5464507	5464508	T	C	22	GENIC	homozygous	109078084
20	5464640	5464641	T	G	24	GENIC	homozygous	109390304
20	5464900	5464901	C	T	17	GENIC	homozygous	109390305
20	5465595	5465596	G	A	12	GENIC	homozygous	109390306
20	5465641	5465642	G	A	26	GENIC	homozygous	109390307