chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230302898	230302899	T	C	12	GENIC	homozygous	60084911
2	230303030	230303031	C	A	15	GENIC	homozygous	59431654
2	230304195	230304196	G	GAA	10	GENIC	possibly homozygous	59431655
2	230304195	230304196	G	GA	10	GENIC	heterozygous	59431656
2	230304206	230304207	G	GAAAAAAAAAAA	8	GENIC	heterozygous	60520629
2	230304514	230304515	G	A	21	GENIC	homozygous	60084912
2	230304700	230304701	A	G	23	GENIC	homozygous	59431657
2	230305038	230305039	C	T	35	GENIC	homozygous	60084913
2	230305068	230305069	G	A	40	GENIC	homozygous	60084914
2	230305144	230305145	T	G	32	GENIC	homozygous	60084915
2	230306189	230306190	G	A	26	GENIC	homozygous	60084916
2	230306357	230306358	A	AAG	12	GENIC	heterozygous	60084917
2	230307158	230307159	A	G	19	GENIC	homozygous	59431664
2	230307400	230307401	A	G	29	GENIC	homozygous	59431665
2	230307530	230307531	A	T	24	GENIC	homozygous	59431666
2	230307630	230307636	TGGGGA	------	19	GENIC	heterozygous	60550442
2	230307866	230307867	T	C	37	GENIC	homozygous	60084918