chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	56892522	56892523	T	G	19	GENIC	homozygous	118452684
13	56892542	56892543	C	G	18	GENIC	homozygous	118452686
13	56892543	56892544	A	G	19	GENIC	homozygous	115025065
13	56892726	56892727	C	G	29	GENIC	homozygous	118452688
13	56892768	56892769	A	C	34	GENIC	homozygous	118452689
13	56892791	56892792	C	T	26	GENIC	homozygous	115025066
13	56892802	56892803	A	T	26	GENIC	homozygous	118452691
13	56892857	56892858	C	G	29	GENIC	homozygous	114359215
13	56892925	56892926	C	A	37	GENIC	homozygous	118452692
13	56892963	56892964	C	T	35	GENIC	homozygous	118452694
13	56893099	56893100	A	G	14	GENIC	homozygous	118452695
13	56893350	56893351	C	T	30	GENIC	homozygous	118452696
13	56893357	56893358	A	G	29	GENIC	homozygous	118452698
13	56893408	56893409	T	G	28	GENIC	homozygous	118452699
13	56893471	56893472	G	A	37	GENIC	homozygous	118452701
13	56893623	56893624	G	C	21	GENIC	homozygous	115010835
13	56892947	56892948	A	G	36	GENIC	homozygous	114768038
13	56893021	56893022	C	G	30	GENIC	homozygous	114677913
13	56893166	56893167	A	G	14	GENIC	homozygous	114554204
13	56893190	56893191	G	A	20	GENIC	homozygous	114554205
13	56893300	56893301	C	A	30	GENIC	homozygous	115100871
13	56893308	56893309	G	A	30	GENIC	homozygous	115100873