chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	48276270	48276271	C	T	21	GENIC	possibly homozygous	113787697
5	48276509	48276510	T	C	24	GENIC	homozygous	114199433
5	48276711	48276712	A	G	37	GENIC	homozygous	113787698
5	48277436	48277437	T	G	26	GENIC	homozygous	113787702
5	48277896	48277897	T	C	31	GENIC	homozygous	114199434
5	48278203	48278204	A	G	17	GENIC	homozygous	113787704
5	48280482	48280483	C	T	38	GENIC	homozygous	114199435
5	48280498	48280499	G	T	38	GENIC	homozygous	114115572
5	48280499	48280500	T	G	38	GENIC	homozygous	114115573
5	48283906	48283907	G	A	20	GENIC	homozygous	114199436
5	48283963	48283964	T	C	21	GENIC	homozygous	113787718
5	48285490	48285491	T	G	35	GENIC	homozygous	114587046
5	48287313	48287314	T	C	25	GENIC	homozygous	113787725
5	48288063	48288064	C	A	32	GENIC	homozygous	113787729
5	48288249	48288250	C	T	24	GENIC	homozygous	114199437
5	48288405	48288406	C	T	27	GENIC	homozygous	113787732
5	48290671	48290672	T	C	41	GENIC	homozygous	113787740
5	48290730	48290731	G	A	36	GENIC	homozygous	114199438
5	48291093	48291094	T	C	25	GENIC	homozygous	113787742
5	48292006	48292007	C	T	25	GENIC	homozygous	114199439
5	48292056	48292057	T	C	35	GENIC	possibly homozygous	114199440