chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	234676088	234676089	C	T	13	GENIC	homozygous	109010812
1	234679895	234679896	T	C	35	GENIC	homozygous	109010814
1	234683777	234683778	G	T	29	GENIC	homozygous	109010816
1	234689203	234689204	A	G	27	GENIC	homozygous	120492313
1	234689204	234689205	T	A	27	GENIC	homozygous	120492314
1	234689793	234689794	A	G	26	GENIC	homozygous	108567265
1	234690348	234690349	G	A	32	GENIC	homozygous	109010818
1	234694555	234694556	T	G	41	GENIC	homozygous	109010819
1	234696971	234696972	C	A	43	GENIC	homozygous	109010820
1	234701288	234701289	C	A	35	GENIC	homozygous	109010821
1	234701464	234701465	T	C	34	GENIC	homozygous	109010822
1	234702126	234702127	C	A	28	GENIC	homozygous	109010823
1	234702598	234702599	G	C	37	GENIC	homozygous	109010824
1	234703570	234703571	G	A	39	GENIC	homozygous	109010826
1	234703603	234703604	A	G	52	GENIC	homozygous	109010827
1	234704652	234704653	A	G	11	GENIC	homozygous	108567275
1	234686648	234686649	G	A	28	GENIC	homozygous	109202229
1	234704302	234704303	T	C	23	GENIC	homozygous	109202231