chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	17239009	17239010	C	T	17	GENIC	homozygous	117682222
9	17239882	17239883	T	C	25	GENIC	possibly homozygous	117682224
9	17239889	17239890	T	C	26	GENIC	possibly homozygous	117682226
9	17239914	17239915	A	G	24	GENIC	possibly homozygous	117270258
9	17240034	17240035	T	C	23	GENIC	possibly homozygous	117270259
9	17241227	17241228	C	G	41	GENIC	homozygous	117682228
9	17242236	17242237	C	T	20	GENIC	homozygous	117682230
9	17243579	17243580	T	G	28	GENIC	possibly homozygous	117682232
9	17244765	17244766	A	C	24	GENIC	homozygous	117682234
9	17247453	17247454	A	C	20	GENIC	possibly homozygous	117768340
9	17247910	17247911	T	C	21	GENIC	homozygous	117682236
9	17252553	17252554	T	G	21	GENIC	homozygous	117682238
9	17252950	17252951	G	T	36	GENIC	homozygous	117682240
9	17252965	17252966	T	C	36	GENIC	homozygous	117682242
9	17253148	17253149	G	C	33	GENIC	homozygous	117682244
9	17253343	17253344	A	G	33	GENIC	homozygous	117682246
9	17253351	17253352	A	G	32	GENIC	homozygous	117682248
9	17253589	17253590	T	A	17	GENIC	homozygous	117682250
9	17254115	17254116	C	T	31	GENIC	homozygous	117682252
9	17254180	17254181	G	T	26	GENIC	homozygous	117682254
9	17254181	17254182	C	T	26	GENIC	homozygous	117682256