chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9706579	9706580	T	A	25	GENIC	homozygous	111230152
17	9707844	9707845	G	A	29	GENIC	homozygous	111295049
17	9708277	9708278	C	G	45	GENIC	homozygous	111230154
17	9710540	9710541	G	T	49	GENIC	homozygous	111230156
17	9711253	9711254	C	T	36	GENIC	homozygous	111230158
17	9711851	9711852	G	A	34	GENIC	possibly homozygous	111230160
17	9712492	9712493	A	G	27	GENIC	homozygous	111230162
17	9712829	9712830	A	G	32	GENIC	homozygous	110952917
17	9712921	9712922	T	C	25	GENIC	homozygous	110952919
17	9713310	9713311	A	C	11	GENIC	homozygous	111230165
17	9713484	9713485	C	T	32	GENIC	homozygous	111230167
17	9713666	9713667	G	A	32	GENIC	homozygous	110952923
17	9715894	9715895	G	A	36	GENIC	homozygous	111230169
17	9716580	9716581	A	G	25	GENIC	homozygous	111230171
17	9717572	9717573	C	T	27	GENIC	homozygous	111295050
17	9717793	9717794	A	C	29	GENIC	homozygous	111230173
17	9718053	9718054	G	A	43	GENIC	homozygous	111230175
17	9718142	9718143	T	C	40	GENIC	homozygous	111230177
17	9718836	9718837	T	C	30	GENIC	homozygous	111230179
17	9719959	9719960	C	T	27	GENIC	homozygous	111230181
17	9720368	9720369	G	A	34	GENIC	homozygous	110952927