chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51849000	51849001	T	C	12	GENIC	homozygous	115355674
12	51849068	51849069	T	C	12	GENIC	homozygous	115355675
12	51850532	51850533	A	G	10	GENIC	homozygous	115355676
12	51852971	51852972	A	G	5	GENIC	homozygous	115355677
12	51853044	51853045	T	A	8	GENIC	homozygous	115355678
12	51854050	51854051	T	C	13	GENIC	homozygous	115355679
12	51856640	51856641	T	C	5	GENIC	homozygous	115355680
12	51856868	51856869	T	C	7	GENIC	homozygous	115355681
12	51860390	51860391	G	A	8	GENIC	homozygous	115355684
12	51860923	51860924	T	C	5	GENIC	homozygous	115355685
12	51861486	51861487	C	T	8	GENIC	homozygous	115355686
12	51861798	51861799	A	G	5	GENIC	homozygous	115355687
12	51862054	51862055	A	C	10	GENIC	homozygous	115355688
12	51862789	51862790	G	A	11	GENIC	homozygous	115355689
12	51862800	51862801	G	T	11	GENIC	homozygous	115355690
12	51863177	51863178	T	C	11	GENIC	homozygous	115355691
12	51864692	51864693	C	T	8	GENIC	homozygous	115355692
12	51866918	51866919	T	G	12	GENIC	homozygous	115355694
12	51867975	51867976	C	T	12	GENIC	homozygous	115355695
12	51869033	51869034	C	T	10	GENIC	homozygous	115355696
12	51869559	51869560	G	A	14	GENIC	homozygous	115355697
12	51870110	51870111	C	T	7	GENIC	homozygous	115355698
12	51871523	51871524	G	A	9	GENIC	homozygous	115355699
12	51873047	51873048	G	A	21	GENIC	homozygous	115404432
12	51874995	51874996	C	A	12	GENIC	homozygous	115355700
12	51874996	51874997	C	A	12	GENIC	homozygous	115355701
12	51875010	51875011	T	G	10	GENIC	homozygous	115355702
12	51876012	51876013	T	C	14	GENIC	homozygous	115355703
12	51876517	51876518	T	C	12	GENIC	homozygous	115355704
12	51876946	51876947	G	C	14	GENIC	homozygous	115355705
12	51877011	51877012	C	T	18	GENIC	homozygous	115355706
12	51877998	51877999	G	C	7	GENIC	homozygous	115355707