chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94715645	94715646	C	T	21	GENIC	possibly homozygous	51748382
10	94716019	94716020	T	A	21	GENIC	possibly homozygous	51748384
10	94716268	94716269	T	C	16	GENIC	homozygous	51748387
10	94716359	94716360	C	T	3	GENIC	homozygous	51748390
10	94718701	94718702	T	C	15	GENIC	possibly homozygous	51748402
10	94718933	94718934	G	C	2	GENIC	homozygous	51748404
10	94718939	94718940	A	G	1	GENIC	homozygous	51549680
10	94719766	94719767	C	G	17	GENIC	possibly homozygous	51748407
10	94719976	94719977	G	A	8	GENIC	possibly homozygous	51748410
10	94720571	94720572	T	C	23	GENIC	homozygous	51748413
10	94721303	94721304	T	TGG	1	GENIC	homozygous	51748416
10	94722059	94722060	G	A	24	GENIC	possibly homozygous	51748421
10	94722172	94722173	C	G	23	GENIC	homozygous	51748424
10	94723954	94723955	A	-	1	GENIC	homozygous	52264417
10	94724635	94724636	A	-	9	GENIC	possibly homozygous	51748438