chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250711935	250711936	T	A	21	GENIC	homozygous	110850746
2	250713684	250713685	C	G	27	GENIC	homozygous	110379613
2	250714444	250714445	T	G	41	GENIC	homozygous	110850748
2	250719517	250719518	T	C	18	GENIC	heterozygous	110850749
2	250719561	250719562	T	C	18	GENIC	heterozygous	110379619
2	250724143	250724144	T	C	18	GENIC	homozygous	110379621
2	250724390	250724391	C	T	20	GENIC	homozygous	110379623
2	250725150	250725151	C	T	29	GENIC	homozygous	110850751
2	250725211	250725212	A	G	27	GENIC	homozygous	110379625
2	250728211	250728212	A	G	22	GENIC	homozygous	110379633
2	250729247	250729248	T	C	17	GENIC	homozygous	110850753
2	250729654	250729655	G	A	24	GENIC	homozygous	110379635
2	250729893	250729894	G	C	32	GENIC	homozygous	110379637
2	250730274	250730275	G	A	25	GENIC	homozygous	110379639
2	250730508	250730509	T	C	26	GENIC	homozygous	110379643
2	250731668	250731669	T	C	19	GENIC	homozygous	110379647
2	250730986	250730987	C	A	29	GENIC	homozygous	110379645
2	250732254	250732255	G	C	20	GENIC	homozygous	110635630
2	250733489	250733490	C	T	29	GENIC	homozygous	110379649
2	250734415	250734416	T	C	27	GENIC	homozygous	110850755
2	250734722	250734723	A	G	25	GENIC	homozygous	110379651
2	250734870	250734871	A	C	17	GENIC	homozygous	110379653
2	250735468	250735469	T	C	17	GENIC	homozygous	110379655
2	250736582	250736583	T	C	26	GENIC	homozygous	110850757
2	250737293	250737294	G	A	19	GENIC	homozygous	110379657
2	250737658	250737659	C	T	21	GENIC	homozygous	110379659
2	250737991	250737992	A	C	19	GENIC	homozygous	110379661
2	250738043	250738044	G	T	14	GENIC	homozygous	110379663
2	250742339	250742340	T	A	23	GENIC	homozygous	110850759
2	250742657	250742658	C	G	18	GENIC	homozygous	110850761
2	250743253	250743254	C	A	27	GENIC	homozygous	110850763
2	250743360	250743361	T	G	31	GENIC	homozygous	110850765