chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25264915	25264916	T	A	11	GENIC	homozygous	115369535
12	25266185	25266186	G	A	12	GENIC	homozygous	115290074
12	25267327	25267328	A	G	11	GENIC	homozygous	115290078
12	25267395	25267396	T	C	9	GENIC	homozygous	115290080
12	25267455	25267456	C	T	8	GENIC	homozygous	115290082
12	25267677	25267678	C	T	16	GENIC	homozygous	115447281
12	25267678	25267679	C	A	17	GENIC	homozygous	115447283
12	25267731	25267732	G	A	16	GENIC	homozygous	115447285
12	25268181	25268182	T	C	23	GENIC	homozygous	115290084
12	25268250	25268251	C	G	24	GENIC	homozygous	115290086
12	25269854	25269855	A	G	11	GENIC	homozygous	115290090
12	25270816	25270817	G	A	22	GENIC	homozygous	115290092
12	25270904	25270905	T	C	21	GENIC	homozygous	115290094
12	25270991	25270992	T	G	11	GENIC	homozygous	115290096
12	25271023	25271024	G	A	9	GENIC	homozygous	115290098
12	25271229	25271230	A	T	14	GENIC	homozygous	115290100
12	25271754	25271755	T	G	11	GENIC	homozygous	115290102
12	25272145	25272146	T	C	13	GENIC	homozygous	115290104
12	25272741	25272742	C	T	22	GENIC	homozygous	115290106
12	25274006	25274007	T	C	13	GENIC	homozygous	115290108
12	25274250	25274251	C	A	13	GENIC	homozygous	115290110
12	25274599	25274600	G	A	13	GENIC	homozygous	115290112