chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17381095	17381096	C	T	29	GENIC	possibly homozygous	50925329
12	17381621	17381622	A	G	30	GENIC	homozygous	50085125
12	17381746	17381747	C	CA	19	GENIC	homozygous	50823250
12	17381912	17381913	C	CAA	14	GENIC	possibly homozygous	50535178
12	17381912	17381913	C	CAAA	14	GENIC	heterozygous	50748308
12	17382014	17382015	A	G	24	GENIC	homozygous	50925332
12	17382118	17382119	C	CA	11	GENIC	homozygous	50880892
12	17382312	17382313	G	T	24	GENIC	homozygous	50718512
12	17382617	17382618	A	G	27	GENIC	homozygous	50823252
12	17383278	17383279	A	-	18	GENIC	homozygous	50718514
12	17385317	17385318	A	G	27	GENIC	homozygous	50823256
12	17385411	17385412	G	A	30	GENIC	homozygous	50925335
12	17385553	17385554	C	T	21	GENIC	possibly homozygous	50925338
12	17385796	17385797	G	A	28	GENIC	homozygous	50925341
12	17386401	17386402	G	-	21	GENIC	homozygous	50880904
12	17386492	17386493	C	T	28	GENIC	homozygous	50880906
12	17386526	17386527	C	CAAA	21	GENIC	homozygous	50557345
12	17387385	17387386	T	G	22	GENIC	homozygous	50718523
12	17387415	17387416	T	C	21	GENIC	homozygous	50718525
12	17387650	17387651	C	G	24	GENIC	homozygous	50925344