chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	9912721	9912722	T	C	25	GENIC	possibly homozygous	109631745
19	9912935	9912936	C	T	21	GENIC	homozygous	109631747
19	9912962	9912963	C	A	27	GENIC	homozygous	109631749
19	9913482	9913483	C	T	17	GENIC	homozygous	109631751
19	9913909	9913910	C	T	29	GENIC	homozygous	109631753
19	9913934	9913935	T	A	36	GENIC	homozygous	109631755
19	9917201	9917202	T	G	19	GENIC	homozygous	109631757
19	9919298	9919299	T	C	27	GENIC	homozygous	109631759
19	9920175	9920176	G	C	18	GENIC	homozygous	109631761
19	9920626	9920627	C	A	18	GENIC	homozygous	109631765
19	9921861	9921862	C	T	27	GENIC	homozygous	109631767
19	9921912	9921913	G	A	31	GENIC	homozygous	109631769
19	9920181	9920182	G	C	17	GENIC	homozygous	109764397
19	9922044	9922045	C	A	27	GENIC	homozygous	109631771
19	9922149	9922150	C	T	22	GENIC	homozygous	109631773
19	9922173	9922174	T	C	26	GENIC	homozygous	109631775
19	9923292	9923293	G	A	26	GENIC	possibly homozygous	109631777
19	9923712	9923713	G	A	20	GENIC	homozygous	109631779
19	9920335	9920336	T	C	4	GENIC	homozygous	109850024
19	9920346	9920347	T	C	2	GENIC	homozygous	110005364
19	9923878	9923879	T	C	27	GENIC	homozygous	109631781
19	9923939	9923940	A	G	21	GENIC	homozygous	109631783
19	9923952	9923953	G	A	21	GENIC	homozygous	109631785
19	9924921	9924922	C	G	37	GENIC	homozygous	109631787
19	9926472	9926473	G	A	18	GENIC	homozygous	109631789
19	9927358	9927359	T	C	20	GENIC	homozygous	109631791
19	9931347	9931348	G	A	17	GENIC	homozygous	109631793
19	9931500	9931501	G	T	20	GENIC	homozygous	109631795