chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54090250	54090251	G	A	19	GENIC	homozygous	52636157
8	54091079	54091080	T	-	15	GENIC	homozygous	52636159
8	54091857	54091858	A	G	20	GENIC	homozygous	53119792
8	54092158	54092159	A	AG	12	GENIC	homozygous	52636161
8	54092404	54092405	T	G	18	GENIC	possibly homozygous	52636163
8	54092559	54092560	A	AT	21	GENIC	homozygous	53698284
8	54094390	54094391	C	CAT	7	GENIC	heterozygous	52636165
8	54094390	54094391	C	CATAT	7	GENIC	possibly homozygous	52976724
8	54095405	54095406	A	AT	15	GENIC	homozygous	52636169
8	54095483	54095484	A	G	15	GENIC	homozygous	53119794
8	54095487	54095488	T	C	14	GENIC	homozygous	52636171
8	54096081	54096082	A	G	20	GENIC	homozygous	52636173
8	54096644	54096645	A	C	15	GENIC	homozygous	53698285
8	54096970	54096971	A	G	11	GENIC	homozygous	52636175
8	54097033	54097034	A	G	13	GENIC	homozygous	52636177
8	54097565	54097584	TCTATCTCAGTGGCCTCTT	-------------------	4	GENIC	homozygous	53387439
8	54098461	54098462	G	A	25	GENIC	homozygous	53698286
8	54098594	54098595	C	T	19	GENIC	homozygous	53698287
8	54098605	54098606	C	T	18	GENIC	homozygous	53119795
8	54099370	54099371	C	A	11	GENIC	homozygous	53698288
8	54099419	54099420	C	A	10	GENIC	homozygous	53119796
8	54100027	54100029	AC	--	1	GENIC	homozygous	53340038
8	54100276	54100277	T	TAA	8	GENIC	homozygous	53119798
8	54100334	54100335	G	GT	19	GENIC	possibly homozygous	53698289
8	54100335	54100336	T	-	19	GENIC	heterozygous	52636191
8	54100639	54100640	G	C	10	GENIC	homozygous	53698290
8	54101108	54101112	AAAC	----	11	GENIC	homozygous	52636201
8	54101664	54101667	AAA	---	4	GENIC	homozygous	53119799
8	54102657	54102658	T	C	11	GENIC	homozygous	52636207
8	54103175	54103176	A	G	21	GENIC	homozygous	52636215
8	54103278	54103279	C	CTTTT	2	GENIC	homozygous	52636217