chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94261039	94261040	C	T	71	GENIC	homozygous	116826196
10	94261354	94261355	C	T	60	GENIC	homozygous	116826198
10	94262555	94262556	T		46	GENIC	homozygous	128847350
10	94262564	94262565	G	A	45	GENIC	homozygous	116826200
10	94262925	94262926	G	T	59	GENIC	homozygous	116826202
10	94266930	94266931	T		69	GENIC	homozygous	128847354
10	94266946	94266946		A	76	GENIC	homozygous	128847355
10	94266986	94266986		A	85	GENIC	homozygous	128847356
10	94266990	94266990		A	87	GENIC	homozygous	128847357
10	94266991	94266991		C	86	GENIC	homozygous	128847358
10	94267025	94267026	T		86	GENIC	homozygous	128847359
10	94267033	94267034	T		87	GENIC	homozygous	128847360
10	94267036	94267037	T		88	GENIC	homozygous	128847361
10	94267225	94267226	T	C	68	GENIC	homozygous	116826204
10	94267259	94267260	A	C	70	GENIC	homozygous	116684998
10	94267259	94267259		C	70	GENIC	homozygous	128847362
10	94267264	94267265	G		70	GENIC	homozygous	128847363
10	94268070	94268071	G	A	76	GENIC	homozygous	116826206
10	94266769	94266770	T	C	1	GENIC	homozygous	117228240
10	94266768	94266769	C	T	2	GENIC	homozygous	117228238