chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207109353	207109354	A	G	5	GENIC	homozygous	59354733
2	207112895	207112901	TGTATA	------	1	GENIC	homozygous	59354741
2	207113473	207113474	T	-	7	GENIC	homozygous	59354748
2	207113672	207113673	C	A	6	GENIC	heterozygous	59354750
2	207114345	207114346	C	T	18	GENIC	possibly homozygous	59354754
2	207114639	207114640	A	G	22	GENIC	possibly homozygous	59354756
2	207115216	207115217	G	-	1	GENIC	homozygous	59354760
2	207116575	207116576	T	C	12	GENIC	homozygous	59354769
2	207116747	207116748	C	T	3	GENIC	heterozygous	59354771
2	207116760	207116761	A	G	12	GENIC	heterozygous	59354773
2	207117080	207117081	G	C	9	GENIC	possibly homozygous	59354774
2	207117197	207117198	T	TCA	1	GENIC	homozygous	59354776
2	207117212	207117213	T	C	7	GENIC	homozygous	59354778
2	207119422	207119423	A	G	21	GENIC	heterozygous	60301105
2	207120039	207120041	TT	--	1	GENIC	homozygous	59354793
2	207121145	207121146	A	AG	9	GENIC	possibly homozygous	59354795
2	207121806	207121807	G	A	13	GENIC	heterozygous	59354797
2	207123577	207123578	G	T	4	GENIC	heterozygous	59354799
2	207123627	207123628	G	-	11	GENIC	possibly homozygous	59354801
2	207124236	207124237	T	G	31	GENIC	possibly homozygous	59354802
2	207124836	207124837	G	T	6	GENIC	homozygous	59354806
2	207125139	207125140	C	G	18	GENIC	homozygous	59354808
2	207125638	207125639	C	G	17	GENIC	heterozygous	59354810
2	207126131	207126139	GATTGATG	--------	10	GENIC	possibly homozygous	59354811
2	207126495	207126496	T	C	22	GENIC	homozygous	59354813
2	207126780	207126781	A	T	22	GENIC	homozygous	59354814
2	207127920	207127921	A	G	8	GENIC	homozygous	59354816