chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59610596	59610597	A	T	8	GENIC	homozygous	53272617
8	59611246	59611247	C	T	12	GENIC	homozygous	53272618
8	59611273	59611274	C	T	14	GENIC	homozygous	53272619
8	59611322	59611323	T	C	14	GENIC	homozygous	52664114
8	59611657	59611658	T	A	37	GENIC	heterozygous	53272620
8	59611783	59611784	T	G	28	GENIC	possibly homozygous	53272621
8	59611887	59611888	G	A	34	GENIC	heterozygous	53272622
8	59617634	59617635	C	T	16	GENIC	homozygous	53272623
8	59617697	59617698	A	G	10	GENIC	possibly homozygous	53272624
8	59617787	59617788	T	C	13	GENIC	homozygous	53272625
8	59618190	59618192	AA	--	13	GENIC	homozygous	53272626
8	59621917	59621918	G	GA	15	GENIC	homozygous	53272627
8	59623745	59623746	C	CT	17	GENIC	homozygous	53272628
8	59624960	59624961	C	T	16	GENIC	heterozygous	52664118
8	59625431	59625432	T	C	8	GENIC	homozygous	53272629
8	59626332	59626333	G	GA	8	GENIC	possibly homozygous	52664120
8	59627299	59627300	T	G	10	GENIC	homozygous	53272630
8	59628168	59628169	C	T	6	GENIC	homozygous	53272631
8	59628386	59628387	C	A	13	GENIC	homozygous	53272632
8	59628711	59628712	G	A	22	GENIC	homozygous	53272633
8	59621901	59621902	T	TA	10	GENIC	heterozygous	52983297