chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51090633	51090634	T	A	21	GENIC	homozygous	52972653
8	51090689	51090690	G	A	27	GENIC	homozygous	52972654
8	51091937	51091938	A	G	14	GENIC	homozygous	52972655
8	51091956	51091958	AA	--	2	GENIC	heterozygous	53386376
8	51093135	51093136	C	G	18	GENIC	homozygous	52972658
8	51093240	51093241	A	G	24	GENIC	homozygous	52972659
8	51093629	51093630	A	G	14	GENIC	homozygous	52972660
8	51094146	51094147	T	A	25	GENIC	homozygous	52972661
8	51094309	51094310	C	T	17	GENIC	homozygous	53697508
8	51095513	51095514	T	C	22	GENIC	homozygous	53116935
8	51095515	51095516	C	T	21	GENIC	homozygous	53363670
8	51096260	51096261	T	TTATCCTCC	24	GENIC	homozygous	52972662
8	51096330	51096331	A	C	20	GENIC	homozygous	52972663
8	51096385	51096386	C	T	25	GENIC	homozygous	52972664
8	51097076	51097077	G	A	26	GENIC	homozygous	52972666
8	51097097	51097098	C	T	23	GENIC	possibly homozygous	53386383
8	51098436	51098437	T	A	40	GENIC	homozygous	53697509
8	51098789	51098791	AT	--	28	GENIC	homozygous	53697510
8	51099074	51099075	C	T	38	GENIC	homozygous	53697511
8	51099112	51099113	T	G	28	GENIC	homozygous	53697512
8	51100015	51100016	G	GAA	10	GENIC	heterozygous	53697513
8	51100180	51100181	G	GTAGTGT	26	GENIC	homozygous	52626226
8	51100542	51100543	C	T	40	GENIC	homozygous	53697514
8	51101514	51101515	A	G	18	GENIC	homozygous	53116941
8	51101818	51101819	C	T	17	GENIC	homozygous	53697515