chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	4556912	4556913	T	A	50	GENIC	homozygous	112447677
15	4563865	4563866	C	G	38	GENIC	homozygous	112447679
15	4563866	4563867	C	T	37	GENIC	homozygous	112447681
15	4563867	4563868	C	G	38	GENIC	homozygous	112447683
15	4563983	4563984	C	G	24	GENIC	homozygous	112447689
15	4563870	4563871	C	G	38	GENIC	homozygous	112447685
15	4563909	4563910	C	G	34	GENIC	homozygous	112447687
15	4573096	4573097	G	T	18	GENIC	homozygous	112447691
15	4574420	4574421	T	A	31	GENIC	homozygous	112447693
15	4574444	4574445	T	C	38	GENIC	homozygous	112447695
15	4574584	4574585	T	C	31	GENIC	homozygous	112447697
15	4574699	4574700	T	C	47	GENIC	homozygous	112447699
15	4574711	4574712	A	C	49	GENIC	homozygous	112447701
15	4574712	4574713	T	A	49	GENIC	homozygous	112447703
15	4574867	4574868	A	T	22	GENIC	homozygous	112447705
15	4591332	4591333	G	C	39	GENIC	homozygous	112447707
15	4591337	4591338	C	G	41	GENIC	homozygous	112447709
15	4591338	4591339	A	T	41	GENIC	homozygous	112447711
15	4591380	4591381	C	G	34	GENIC	homozygous	112447713