chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	224854547	224854548	G	A	19	GENIC	homozygous	57112597
4	224854874	224854875	C	G	6	GENIC	homozygous	57112600
4	224854882	224854883	C	T	11	GENIC	possibly homozygous	57112602
4	224857816	224857817	C	T	17	GENIC	heterozygous	57112625
4	224858318	224858319	T	C	5	GENIC	homozygous	57112627
4	224858530	224858531	A	C	21	GENIC	homozygous	57112629
4	224858803	224858804	A	G	23	GENIC	homozygous	57112631
4	224859155	224859156	C	T	16	GENIC	heterozygous	57112633
4	224859712	224859713	A	G	31	GENIC	possibly homozygous	57112636
4	224860556	224860557	C	T	33	GENIC	possibly homozygous	57112638
4	224860679	224860680	T	C	14	GENIC	possibly homozygous	57112639
4	224861526	224861527	T	C	9	GENIC	homozygous	57112641
4	224861563	224861564	C	T	24	GENIC	homozygous	57112643
4	224861932	224861933	A	G	12	GENIC	homozygous	57112645
4	224861996	224861997	T	C	1	GENIC	homozygous	57112647
4	224862369	224862370	T	C	15	GENIC	possibly homozygous	57112651
4	224862844	224862845	G	A	35	GENIC	possibly homozygous	57112653
4	224863155	224863156	G	A	17	GENIC	heterozygous	57112655
4	224863771	224863772	T	C	11	GENIC	homozygous	57112656
4	224864670	224864671	G	A	16	GENIC	heterozygous	57112672
4	224864907	224864908	G	A	12	GENIC	heterozygous	57112673
4	224865416	224865417	C	T	22	GENIC	homozygous	57112675
4	224867581	224867582	C	T	15	GENIC	homozygous	57112677
4	224868401	224868402	T	C	12	GENIC	possibly homozygous	57112678
4	224868507	224868508	C	T	9	GENIC	homozygous	57112680
4	224871043	224871044	T	G	17	GENIC	homozygous	57112682
4	224871413	224871414	A	G	33	GENIC	possibly homozygous	57112684
4	224871987	224871988	A	-	3	GENIC	heterozygous	58023890
4	224873382	224873386	TCTG	----	2	GENIC	homozygous	57112687