chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	17125514	17125515	C	T	30	GENIC	homozygous	117682042
9	17127801	17127802	G	A	38	GENIC	homozygous	117682044
9	17127836	17127837	A	C	37	GENIC	homozygous	117270154
9	17128167	17128168	C	G	26	GENIC	homozygous	117270155
9	17128513	17128514	A	G	34	GENIC	homozygous	117682046
9	17128541	17128542	G	T	39	GENIC	homozygous	117682048
9	17128544	17128545	G	A	40	GENIC	homozygous	117682050
9	17131897	17131898	T	A	39	GENIC	homozygous	117270157
9	17135260	17135261	G	C	44	GENIC	homozygous	117270159
9	17135524	17135525	G	A	33	GENIC	homozygous	117682052
9	17135565	17135566	G	A	32	GENIC	possibly homozygous	117270160
9	17141804	17141805	G	A	24	GENIC	homozygous	117682054
9	17145093	17145094	G	A	21	GENIC	homozygous	117682056
9	17147795	17147796	G	A	18	GENIC	homozygous	117682058
9	17147834	17147835	G	T	17	GENIC	homozygous	117270163
9	17150229	17150230	G	A	24	GENIC	homozygous	117462723
9	17150230	17150231	A	G	24	GENIC	homozygous	117462724
9	17153426	17153427	T	G	27	GENIC	homozygous	117682062
9	17156128	17156129	T	C	34	GENIC	homozygous	117270170
9	17156286	17156287	A	G	27	GENIC	homozygous	117270171
9	17160584	17160585	A	G	16	GENIC	homozygous	120362523
9	17161137	17161138	A	G	30	GENIC	possibly homozygous	117270173
9	17162247	17162248	T	C	18	GENIC	possibly homozygous	117270174
9	17162774	17162775	G	A	16	GENIC	homozygous	117270175