chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	64965286	64965287	A	G	43	GENIC	homozygous	46187746
19	64965914	64965915	C	T	25	GENIC	homozygous	46187747
19	64966182	64966183	G	A	22	GENIC	homozygous	46187748
19	64966275	64966276	T	A	15	GENIC	homozygous	46187749
19	64967071	64967072	C	T	32	GENIC	homozygous	46187750
19	64967666	64967667	T	C	32	GENIC	homozygous	46187751
19	64968361	64968362	C	G	34	GENIC	homozygous	46187752
19	64968569	64968573	GTAT	----	19	GENIC	homozygous	46187753
19	64968715	64968716	C	T	19	GENIC	homozygous	46187754
19	64968738	64968739	G	A	10	GENIC	possibly homozygous	46187755
19	64968972	64968973	T	-	21	GENIC	homozygous	46187756
19	64968991	64968992	A	G	26	GENIC	homozygous	46187757
19	64969071	64969072	A	G	34	GENIC	homozygous	46187758
19	64969193	64969194	A	G	39	GENIC	homozygous	46187759
19	64969706	64969707	C	T	24	GENIC	homozygous	46187760
19	64969810	64969811	A	G	41	GENIC	homozygous	46187761
19	64969905	64969906	C	T	49	GENIC	heterozygous	46187762
19	64970329	64970330	G	A	26	GENIC	homozygous	46187763
19	64970502	64970503	T	A	32	GENIC	homozygous	46187764
19	64971160	64971161	C	T	31	GENIC	homozygous	46187765
19	64971399	64971400	G	A	36	GENIC	heterozygous	46187766
19	64971497	64971498	T	C	34	GENIC	heterozygous	46187767