chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	9912721	9912722	T	C	42	GENIC	possibly homozygous	109631745
19	9912935	9912936	C	T	50	GENIC	homozygous	109631747
19	9912962	9912963	C	A	48	GENIC	possibly homozygous	109631749
19	9913482	9913483	C	T	51	GENIC	homozygous	109631751
19	9913909	9913910	C	T	44	GENIC	homozygous	109631753
19	9913934	9913935	T	A	46	GENIC	homozygous	109631755
19	9917201	9917202	T	G	42	GENIC	homozygous	109631757
19	9919298	9919299	T	C	67	GENIC	homozygous	109631759
19	9920175	9920176	G	C	35	GENIC	homozygous	109631761
19	9920626	9920627	C	A	29	GENIC	homozygous	109631765
19	9921861	9921862	C	T	45	GENIC	homozygous	109631767
19	9921912	9921913	G	A	55	GENIC	homozygous	109631769
19	9922044	9922045	C	A	49	GENIC	homozygous	109631771
19	9922149	9922150	C	T	45	GENIC	homozygous	109631773
19	9922173	9922174	T	C	51	GENIC	homozygous	109631775
19	9923292	9923293	G	A	44	GENIC	homozygous	109631777
19	9923712	9923713	G	A	51	GENIC	homozygous	109631779
19	9923878	9923879	T	C	65	GENIC	homozygous	109631781
19	9923939	9923940	A	G	67	GENIC	homozygous	109631783
19	9923952	9923953	G	A	67	GENIC	homozygous	109631785
19	9924921	9924922	C	G	59	GENIC	homozygous	109631787
19	9926472	9926473	G	A	36	GENIC	homozygous	109631789
19	9927358	9927359	T	C	52	GENIC	homozygous	109631791
19	9931347	9931348	G	A	43	GENIC	homozygous	109631793
19	9931500	9931501	G	T	46	GENIC	possibly homozygous	109631795
19	9925920	9925921	T	G	46	GENIC	heterozygous	119715955