chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62528876	62528877	G	A	35	GENIC	homozygous	117110005
8	62529025	62529026	A	G	31	GENIC	homozygous	117110006
8	62529916	62529917	G	A	19	GENIC	homozygous	117110007
8	62529935	62529936	G	T	19	GENIC	homozygous	116836795
8	62530353	62530355	TG		26	GENIC	homozygous	130363513
8	62530382	62530383	T	C	31	GENIC	homozygous	117110008
8	62530481	62530483	TT		30	GENIC	possibly homozygous	130363514
8	62530669	62530670	C		11	GENIC	homozygous	130363515
8	62531406	62531407	T	C	24	GENIC	homozygous	117110009
8	62531825	62531826	T	G	28	GENIC	homozygous	117110010
8	62532475	62532476	A	G	21	GENIC	homozygous	117110011
8	62532655	62532656	A	G	25	GENIC	homozygous	117110012
8	62533899	62533900	C	G	21	GENIC	heterozygous	117110013
8	62533899	62533899		G	21	GENIC	heterozygous	130363516
8	62534605	62534606	A	G	33	GENIC	homozygous	117110014
8	62537427	62537428	T	G	27	GENIC	homozygous	116836799
8	62537660	62537661	A		18	GENIC	homozygous	130363517
8	62537841	62537842	A	G	30	GENIC	homozygous	116836801
8	62539036	62539037	T	G	35	GENIC	homozygous	116836805
8	62539431	62539432	A	G	24	GENIC	homozygous	116836807
8	62539815	62539816	T	A	23	GENIC	homozygous	116836809
8	62539952	62539953	G	A	37	GENIC	homozygous	116836811
8	62541787	62541788	C	T	33	GENIC	homozygous	117158239