chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51090633	51090634	T	A	24	GENIC	homozygous	52972653
8	51090910	51090911	C	T	21	GENIC	possibly homozygous	53116927
8	51091723	51091724	C	G	20	GENIC	homozygous	53116928
8	51091835	51091836	T	C	20	GENIC	homozygous	53116929
8	51091937	51091938	A	G	13	GENIC	homozygous	52972655
8	51093135	51093136	C	G	15	GENIC	homozygous	52972658
8	51093240	51093241	A	G	26	GENIC	homozygous	52972659
8	51093946	51093947	A	G	29	GENIC	homozygous	53116931
8	51094073	51094074	A	G	35	GENIC	homozygous	53116932
8	51094093	51094094	G	A	33	GENIC	homozygous	53116933
8	51094146	51094147	T	A	24	GENIC	homozygous	52972661
8	51094777	51094778	T	C	19	GENIC	homozygous	53116934
8	51095513	51095514	T	C	17	GENIC	homozygous	53116935
8	51097658	51097659	T	C	25	GENIC	homozygous	53116936
8	51097815	51097816	A	G	15	GENIC	homozygous	53116937
8	51097960	51097961	A	G	22	GENIC	homozygous	53116938
8	51099090	51099091	G	A	17	GENIC	homozygous	53116939
8	51100180	51100181	G	GTAGTGT	22	GENIC	homozygous	52626226
8	51101225	51101226	G	-	15	GENIC	possibly homozygous	53116940
8	51101514	51101515	A	G	17	GENIC	homozygous	53116941
8	51101647	51101648	C	T	25	GENIC	homozygous	53116942
8	51101899	51101900	A	C	12	GENIC	homozygous	53116946