chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51908703	51908704	C	T	21	GENIC	homozygous	115355736
12	51908767	51908768	A	G	23	GENIC	homozygous	115355737
12	51909927	51909928	C	G	45	GENIC	homozygous	115355738
12	51910914	51910915	C	G	30	GENIC	homozygous	115355739
12	51911918	51911919	C	T	14	GENIC	homozygous	115355740
12	51912497	51912498	A	G	24	GENIC	homozygous	115404448
12	51913809	51913810	T	A	34	GENIC	homozygous	115404450
12	51915430	51915431	A	T	17	GENIC	homozygous	115355741
12	51915839	51915840	G	A	17	GENIC	homozygous	115355742
12	51918077	51918078	T	C	33	GENIC	homozygous	115355743
12	51919580	51919581	C	A	39	GENIC	homozygous	115355744
12	51919707	51919708	C	A	49	GENIC	homozygous	115355745
12	51919785	51919786	G	A	42	GENIC	homozygous	115355746
12	51920677	51920678	C	T	28	GENIC	homozygous	115355747
12	51920935	51920936	A	C	34	GENIC	homozygous	115355748
12	51921195	51921196	C	T	44	GENIC	homozygous	115355749
12	51921429	51921430	G	A	34	GENIC	homozygous	115355750
12	51923452	51923453	T	G	48	GENIC	homozygous	115355752
12	51924161	51924162	T	C	36	GENIC	homozygous	115355753
12	51924480	51924481	G	A	29	GENIC	homozygous	115355754
12	51926557	51926558	A	G	37	GENIC	homozygous	115355755
12	51926652	51926653	C	T	22	GENIC	homozygous	115355756
12	51927793	51927794	A	G	32	GENIC	homozygous	115355757
12	51929118	51929119	C	T	37	GENIC	homozygous	115355758
12	51929470	51929471	G	A	21	GENIC	homozygous	115355759
12	51929731	51929732	T	C	26	GENIC	homozygous	115355760
12	51929858	51929859	C	T	25	GENIC	homozygous	115355761
12	51930052	51930053	C	T	32	GENIC	homozygous	115355762
12	51930838	51930839	G	A	28	GENIC	homozygous	115355763
12	51930999	51931000	T	C	32	GENIC	homozygous	115355764
12	51932453	51932454	C	T	35	GENIC	homozygous	115355765
12	51934221	51934222	A	G	45	GENIC	homozygous	115355766