chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51090633	51090634	T	A	24	GENIC	homozygous	52972653
8	51090689	51090690	G	A	28	GENIC	homozygous	52972654
8	51091937	51091938	A	G	8	GENIC	homozygous	52972655
8	51093135	51093136	C	G	25	GENIC	homozygous	52972658
8	51093240	51093241	A	G	27	GENIC	homozygous	52972659
8	51093629	51093630	A	G	34	GENIC	homozygous	52972660
8	51094146	51094147	T	A	33	GENIC	homozygous	52972661
8	51095513	51095514	T	C	23	GENIC	homozygous	53116935
8	51095515	51095516	C	T	23	GENIC	homozygous	53363670
8	51096260	51096261	T	TTATCCTCC	25	GENIC	homozygous	52972662
8	51096330	51096331	A	C	31	GENIC	homozygous	52972663
8	51096385	51096386	C	T	36	GENIC	homozygous	52972664
8	51096886	51096887	T	C	33	GENIC	homozygous	52972665
8	51097076	51097077	G	A	25	GENIC	homozygous	52972666
8	51097635	51097636	C	CA	21	GENIC	homozygous	52972667
8	51100180	51100181	G	GTAGTGT	20	GENIC	homozygous	52626226