chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	250756689	250756690	T	C	5	GENIC	homozygous	110850802
2	250756690	250756691	G	A	5	GENIC	homozygous	110850804
2	250756734	250756735	T	G	7	GENIC	homozygous	110850806
2	250757209	250757210	G	A	21	GENIC	homozygous	110850809
2	250759109	250759110	G	A	19	GENIC	homozygous	110850811
2	250759297	250759298	T	C	26	GENIC	homozygous	110850813
2	250760584	250760585	A	G	14	GENIC	homozygous	110850817
2	250761408	250761409	A	T	12	GENIC	homozygous	110850819
2	250761434	250761435	T	C	14	GENIC	homozygous	110850821
2	250763008	250763009	A	G	19	GENIC	homozygous	110850823
2	250763966	250763967	G	C	12	GENIC	heterozygous	110850825
2	250764258	250764259	C	T	7	GENIC	homozygous	110850827
2	250764635	250764636	T	C	17	GENIC	homozygous	110379704
2	250764750	250764751	C	A	23	GENIC	homozygous	110379714
2	250764845	250764846	A	T	19	GENIC	homozygous	110379721
2	250765003	250765004	C	T	23	GENIC	homozygous	110379722
2	250765178	250765179	G	A	16	GENIC	homozygous	110379724
2	250772060	250772061	G	C	17	GENIC	homozygous	111292786