chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	121884366	121884367	G	A	27	GENIC	homozygous	56889335
5	121884517	121884519	TT	--	21	GENIC	heterozygous	56617963
5	121884518	121884519	T	-	21	GENIC	heterozygous	56573369
5	121884603	121884604	C	T	29	GENIC	homozygous	57274895
5	121884604	121884605	A	G	28	GENIC	homozygous	57274898
5	121885178	121885179	A	G	30	GENIC	possibly homozygous	57274901
5	121885564	121885565	C	T	22	GENIC	possibly homozygous	57274904
5	121885953	121885954	C	T	21	GENIC	homozygous	57274907
5	121886073	121886074	A	T	12	GENIC	homozygous	57274910
5	121886497	121886498	T	C	28	GENIC	homozygous	57274913
5	121887249	121887250	T	C	23	GENIC	homozygous	57274916
5	121887492	121887493	G	T	28	GENIC	possibly homozygous	57274918
5	121887525	121887526	C	T	30	GENIC	possibly homozygous	57274921
5	121887564	121887565	T	C	28	GENIC	possibly homozygous	57274924
5	121887806	121887807	A	T	32	GENIC	homozygous	57274927
5	121888103	121888104	T	A	26	GENIC	homozygous	57274930
5	121888568	121888569	G	A	33	GENIC	homozygous	57274933
5	121889316	121889317	A	AAAAAG	13	GENIC	possibly homozygous	57274936
5	121889386	121889387	C	T	19	GENIC	homozygous	57274939
5	121886496	121886497	G	T	28	GENIC	homozygous	56185346