chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	245812198	245812199	C	CA	2	GENIC	heterozygous	57191810
4	245812409	245812410	C	A	12	GENIC	homozygous	57191812
4	245812860	245812861	C	G	18	GENIC	homozygous	57191814
4	245812888	245812889	T	C	20	GENIC	possibly homozygous	57191816
4	245813096	245813097	C	T	15	GENIC	possibly homozygous	57191818
4	245813396	245813397	C	A	15	GENIC	homozygous	57191820
4	245813611	245813612	G	-	15	GENIC	homozygous	57191822
4	245813613	245813618	TGATG	-----	2	GENIC	homozygous	57191824
4	245813620	245813621	G	A	2	GENIC	homozygous	57684340
4	245817567	245817568	G	A	22	GENIC	possibly homozygous	57191828
4	245818210	245818211	C	T	30	GENIC	homozygous	57191830
4	245818639	245818640	G	A	19	GENIC	possibly homozygous	57191832
4	245819189	245819190	C	A	18	GENIC	possibly homozygous	57191834
4	245819313	245819314	T	G	20	GENIC	possibly homozygous	57191836
4	245819692	245819693	T	A	9	GENIC	heterozygous	57191838
4	245819887	245819888	A	C	20	GENIC	possibly homozygous	57191840
4	245820266	245820268	AA	--	2	GENIC	homozygous	57191842
4	245820417	245820418	A	T	4	GENIC	homozygous	57191846
4	245820619	245820620	A	G	24	GENIC	homozygous	57191848
4	245821305	245821306	C	T	23	GENIC	homozygous	57191852