chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	240588006	240588007	A	T	22	GENIC	homozygous	110334534
2	240588232	240588233	T	C	13	GENIC	heterozygous	110334536
2	240588874	240588875	A	G	15	GENIC	homozygous	110334538
2	240589176	240589177	G	A	17	GENIC	homozygous	110334540
2	240589561	240589562	T	C	14	GENIC	homozygous	110334543
2	240590210	240590211	T	C	22	GENIC	possibly homozygous	110334545
2	240590530	240590531	A	G	14	GENIC	homozygous	110334547
2	240590794	240590795	A	G	13	GENIC	homozygous	110334549
2	240597333	240597334	T	C	14	GENIC	homozygous	110334557
2	240597497	240597498	G	T	21	GENIC	homozygous	110334559
2	240597782	240597783	C	G	25	GENIC	homozygous	110334561
2	240599162	240599163	T	C	23	GENIC	homozygous	110334565
2	240599643	240599644	C	A	27	GENIC	homozygous	110334567
2	240600002	240600003	C	T	15	GENIC	homozygous	110334569
2	240601493	240601494	G	A	10	GENIC	possibly homozygous	110334571
2	240601781	240601782	T	C	17	GENIC	homozygous	110334573
2	240603011	240603012	A	G	26	GENIC	homozygous	110334575
2	240603954	240603955	G	A	15	GENIC	homozygous	110334579
2	240604236	240604237	A	G	31	GENIC	homozygous	110334581
2	240604383	240604384	T	G	25	GENIC	homozygous	110334583
2	240604969	240604970	A	G	25	GENIC	homozygous	110334585
2	240605200	240605201	G	A	33	GENIC	homozygous	110334587
2	240605740	240605741	C	T	25	GENIC	possibly homozygous	110334589
2	240606636	240606637	G	C	29	GENIC	possibly homozygous	110334591
2	240608294	240608295	C	A	32	GENIC	homozygous	110334595
2	240608560	240608561	C	G	14	GENIC	homozygous	110334597
2	240608629	240608630	A	C	19	GENIC	possibly homozygous	110334599
2	240610255	240610256	A	G	26	GENIC	homozygous	110334601