chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5113261	5113262	G	A	7	GENIC	homozygous	109076943
20	5113349	5113350	C	T	10	GENIC	homozygous	109076945
20	5113767	5113768	T	G	11	GENIC	homozygous	109076947
20	5114216	5114217	G	A	22	GENIC	homozygous	109076949
20	5114217	5114218	A	T	23	GENIC	homozygous	109076951
20	5114245	5114246	C	A	20	GENIC	homozygous	109076953
20	5114246	5114247	C	G	22	GENIC	homozygous	109076955
20	5114250	5114251	T	G	23	GENIC	homozygous	109076957
20	5114354	5114355	C	T	19	GENIC	homozygous	109076959
20	5114692	5114693	T	C	21	GENIC	homozygous	109076961
20	5114766	5114767	G	T	16	GENIC	homozygous	109076963
20	5114828	5114829	T	C	12	GENIC	homozygous	109076965
20	5114850	5114851	G	A	17	GENIC	homozygous	109076967
20	5115053	5115054	C	T	10	GENIC	homozygous	109296829
20	5115664	5115665	A	G	19	GENIC	homozygous	109076971
20	5115871	5115872	G	A	18	GENIC	homozygous	109076973
20	5115932	5115933	G	A	15	GENIC	homozygous	109076975
20	5116049	5116050	A	G	26	GENIC	homozygous	109076977