chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	103578245	103578246	T	C	37	GENIC	homozygous	112630352
15	103580229	103580230	C	T	40	GENIC	homozygous	112630354
15	103581543	103581544	G	T	56	GENIC	homozygous	112630356
15	103581721	103581722	T	C	51	GENIC	homozygous	112630358
15	103581945	103581946	T	C	33	GENIC	homozygous	112630360
15	103582491	103582492	T	G	47	GENIC	homozygous	112630362
15	103582583	103582584	A	G	42	GENIC	homozygous	112630364
15	103583347	103583348	C	T	47	GENIC	homozygous	112630366
15	103583379	103583380	T	C	37	GENIC	homozygous	112630368
15	103583590	103583591	A	G	53	GENIC	homozygous	112630371
15	103584931	103584932	T	A	36	GENIC	homozygous	112630373
15	103585919	103585920	G	C	31	GENIC	homozygous	112630375
15	103586107	103586108	C	A	45	GENIC	possibly homozygous	112630377
15	103587372	103587373	A	G	42	GENIC	homozygous	112630379
15	103588386	103588387	A	T	34	GENIC	homozygous	112630381