chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62708046	62708047	A	G	30	GENIC	homozygous	113236008
4	62717445	62717446	A	G	19	GENIC	homozygous	112673079
4	62725345	62725346	G	C	23	GENIC	homozygous	113236009
4	62727808	62727809	G	A	19	GENIC	homozygous	112673085
4	62734504	62734505	G	A	22	GENIC	homozygous	112673089
4	62737854	62737855	C	A	19	GENIC	homozygous	113236010
4	62739427	62739428	T	C	24	GENIC	homozygous	112673099
4	62739549	62739550	C	T	26	GENIC	homozygous	113236011
4	62739704	62739705	G	T	20	GENIC	homozygous	112673101
4	62740486	62740487	C	A	23	GENIC	homozygous	112673103
4	62742678	62742679	A	C	21	GENIC	homozygous	113236012
4	62745428	62745429	T	C	20	GENIC	homozygous	113236013
4	62745463	62745464	C	T	22	GENIC	homozygous	113236014
4	62747794	62747795	C	A	12	GENIC	homozygous	113236015
4	62748271	62748272	T	C	24	GENIC	homozygous	112673105
4	62750469	62750470	G	A	19	GENIC	homozygous	112673109
4	62750484	62750485	T	C	16	GENIC	homozygous	112673111
4	62755419	62755420	G	A	21	GENIC	homozygous	112673115
4	62757953	62757954	C	T	26	GENIC	homozygous	113236016
4	62758656	62758657	G	A	11	GENIC	homozygous	112673117
4	62759721	62759722	A	G	24	GENIC	homozygous	113236017
4	62766585	62766586	T	C	26	GENIC	homozygous	112673121
4	62769465	62769466	T	G	8	GENIC	homozygous	112673131
4	62772474	62772475	T	C	14	GENIC	homozygous	112673137
4	62772774	62772775	A	G	16	GENIC	homozygous	113236018