chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54090117	54090118	G	A	22	GENIC	homozygous	52636155
8	54090250	54090251	G	A	24	GENIC	homozygous	52636157
8	54090789	54090790	G	A	21	GENIC	homozygous	52976723
8	54091079	54091080	T	-	16	GENIC	homozygous	52636159
8	54092158	54092159	A	AG	35	GENIC	homozygous	52636161
8	54094390	54094391	C	CATAT	6	GENIC	homozygous	52976724
8	54095022	54095023	T	A	14	GENIC	homozygous	52976725
8	54095405	54095406	A	AT	35	GENIC	possibly homozygous	52636169
8	54095541	54095542	T	G	31	GENIC	homozygous	52976726
8	54096081	54096082	A	G	24	GENIC	homozygous	52636173
8	54096433	54096434	A	C	26	GENIC	homozygous	52976727
8	54096970	54096971	A	G	17	GENIC	homozygous	52636175
8	54097033	54097034	A	G	28	GENIC	homozygous	52636177
8	54098606	54098607	G	T	27	GENIC	homozygous	52976728
8	54100012	54100013	T	TAC	9	GENIC	heterozygous	52976729
8	54100027	54100029	AC	--	9	GENIC	heterozygous	53340038
8	54100049	54100050	G	A	17	GENIC	possibly homozygous	52976730
8	54100276	54100277	T	TA	10	GENIC	heterozygous	52636189
8	54100276	54100277	T	TAA	10	GENIC	heterozygous	53119798
8	54101095	54101096	A	AC	19	GENIC	homozygous	52976731
8	54101107	54101108	A	AAAAC	15	GENIC	homozygous	52976732
8	54101486	54101487	C	T	21	GENIC	homozygous	52976733
8	54102494	54102495	C	CTTTT	14	GENIC	homozygous	52976734
8	54102657	54102658	T	C	24	GENIC	homozygous	52636207
8	54102781	54102791	GTTGTGTGCA	----------	10	GENIC	homozygous	52636209
8	54103175	54103176	A	G	22	GENIC	homozygous	52636215
8	54103211	54103212	A	C	20	GENIC	homozygous	52976735
8	54101663	54101664	C	CAAA	4	GENIC	heterozygous	53431420
8	54103288	54103289	T	TTTTTTTTTTGC	6	GENIC	heterozygous	53431422
8	54103288	54103289	T	TTTTTTTTTGC	6	GENIC	heterozygous	53507868