chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51908703	51908704	C	T	9	GENIC	homozygous	115355736
12	51908767	51908768	A	G	14	GENIC	homozygous	115355737
12	51909927	51909928	C	G	8	GENIC	homozygous	115355738
12	51910914	51910915	C	G	17	GENIC	homozygous	115355739
12	51911918	51911919	C	T	11	GENIC	homozygous	115355740
12	51912497	51912498	A	G	19	GENIC	homozygous	115404448
12	51913581	51913582	G	A	5	GENIC	homozygous	126222611
12	51913809	51913810	T	A	17	GENIC	homozygous	115404450
12	51915430	51915431	A	T	22	GENIC	homozygous	115355741
12	51915839	51915840	G	A	10	GENIC	homozygous	115355742
12	51918077	51918078	T	C	19	GENIC	homozygous	115355743
12	51919580	51919581	C	A	26	GENIC	homozygous	115355744
12	51919707	51919708	C	A	19	GENIC	homozygous	115355745
12	51919785	51919786	G	A	25	GENIC	homozygous	115355746
12	51920677	51920678	C	T	22	GENIC	homozygous	115355747
12	51920935	51920936	A	C	10	GENIC	homozygous	115355748
12	51921195	51921196	C	T	13	GENIC	homozygous	115355749
12	51921429	51921430	G	A	27	GENIC	homozygous	115355750
12	51923222	51923223	C	T	17	GENIC	homozygous	115355751
12	51923452	51923453	T	G	22	GENIC	homozygous	115355752
12	51924480	51924481	G	A	14	GENIC	homozygous	115355754
12	51926557	51926558	A	G	19	GENIC	homozygous	115355755
12	51926652	51926653	C	T	10	GENIC	homozygous	115355756
12	51927793	51927794	A	G	13	GENIC	homozygous	115355757
12	51929385	51929386	T	G	8	GENIC	homozygous	126175808
12	51929470	51929471	G	A	20	GENIC	homozygous	115355759
12	51929731	51929732	T	C	12	GENIC	homozygous	115355760
12	51930838	51930839	G	A	15	GENIC	homozygous	115355763
12	51930999	51931000	T	C	9	GENIC	homozygous	115355764
12	51932453	51932454	C	T	19	GENIC	homozygous	115355765
12	51933789	51933790	C	T	11	GENIC	homozygous	126224926
12	51934221	51934222	A	G	22	GENIC	homozygous	115355766