chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88357344	88357345	C	G	19	GENIC	homozygous	116901396
10	88357671	88357672	A	G	22	GENIC	possibly homozygous	116901398
10	88360060	88360061	A	G	16	GENIC	homozygous	116901400
10	88360512	88360513	G	A	24	GENIC	homozygous	116901402
10	88361494	88361495	G	T	39	GENIC	homozygous	116901406
10	88362458	88362459	C	T	25	GENIC	homozygous	116901408
10	88364088	88364089	G	A	37	GENIC	homozygous	116673660
10	88364542	88364543	A	G	25	GENIC	homozygous	116901410
10	88367387	88367388	A	G	14	GENIC	homozygous	116818859
10	88367433	88367434	G	A	14	GENIC	homozygous	116901414
10	88367904	88367905	T	G	28	GENIC	homozygous	116673666
10	88367983	88367984	T	G	24	GENIC	homozygous	116818861
10	88367989	88367990	T	C	21	GENIC	homozygous	116673668
10	88368068	88368069	T	G	24	GENIC	homozygous	116818863
10	88368219	88368220	A	G	6	GENIC	homozygous	116673672
10	88368623	88368624	A	G	28	GENIC	homozygous	116673674
10	88368735	88368736	T	C	29	GENIC	homozygous	116673676
10	88368830	88368831	T	G	19	GENIC	homozygous	116673678
10	88369071	88369072	T	G	20	GENIC	homozygous	116673680
10	88369298	88369299	T	A	32	GENIC	homozygous	116982442
10	88369299	88369300	T	A	32	GENIC	homozygous	116982444
10	88369338	88369339	C	G	32	GENIC	homozygous	116818877
10	88370833	88370834	A	C	30	GENIC	homozygous	116673684
10	88372436	88372437	C	T	29	GENIC	homozygous	116901418