chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	16150559	16150560	C	T	46	GENIC	homozygous	142043806
8	16150593	16150594	T	G	45	GENIC	homozygous	142043807
8	16150602	16150603	A	G	45	GENIC	homozygous	142043808
8	16150637	16150638	G	A	42	GENIC	homozygous	142043809
8	16150779	16150780	G	C	43	GENIC	homozygous	142043810
8	16151057	16151058	C	T	51	GENIC	homozygous	142043811
8	16151144	16151145	T	C	47	GENIC	homozygous	142043812
8	16151181	16151182	G	A	43	GENIC	homozygous	142043813
8	16151350	16151351	C	T	51	GENIC	homozygous	142043814
8	16151946	16151947	G	A	66	GENIC	homozygous	142043815
8	16152254	16152255	G	A	40	GENIC	homozygous	142043816
8	16152296	16152297	A	G	38	GENIC	possibly homozygous	142043817
8	16152364	16152365	C	T	38	GENIC	possibly homozygous	142043818
8	16152572	16152573	A	G	31	GENIC	homozygous	142043819
8	16156089	16156090	G	A	38	GENIC	homozygous	142043844
8	16155117	16155118	T	G	50	GENIC	homozygous	142043836
8	16155575	16155576	G	T	35	GENIC	possibly homozygous	142043840
8	16159592	16159593	C	T	48	GENIC	homozygous	142043850
8	16159342	16159343	T	C	50	GENIC	homozygous	143389149
8	16152195	16152198	AAG		35	GENIC	homozygous	142018596
8	16154418	16154418		T	48	GENIC	homozygous	143375345
8	16155760	16155761	A	C	10	GENIC	homozygous	154502158
8	16155768	16155769	C	A	11	GENIC	homozygous	154502159
8	16155768	16155769	C		11	GENIC	heterozygous	403230438