chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39991688	39991689	A	G	30	GENIC	homozygous	52963587
8	39992389	39992390	T	TTG	27	GENIC	homozygous	52963588
8	39992851	39992852	G	A	29	GENIC	homozygous	52963589
8	39992885	39992886	G	T	25	GENIC	homozygous	52963590
8	39993319	39993320	C	T	28	GENIC	homozygous	52963591
8	39993456	39993457	A	G	23	GENIC	homozygous	52963592
8	39995070	39995071	T	TAA	12	GENIC	heterozygous	52963593
8	39995070	39995071	T	TA	12	GENIC	possibly homozygous	52963594
8	39995334	39995335	C	A	42	GENIC	homozygous	52963595
8	39995688	39995689	A	G	29	GENIC	homozygous	52963596
8	39995751	39995752	G	A	33	GENIC	homozygous	52963597