chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100849165	100849166	C	T	36	GENIC	homozygous	120283413
9	100849876	100849877	C	T	62	GENIC	homozygous	117400469
9	100849923	100849924	A	C	57	GENIC	homozygous	117400470
9	100850066	100850067	G	A	70	GENIC	homozygous	120283414
9	100850507	100850508	A	G	53	GENIC	homozygous	117620189
9	100851536	100851537	G	A	27	GENIC	homozygous	120283415
9	100851661	100851662	C	T	29	GENIC	homozygous	120283416
9	100853680	100853681	G	A	42	GENIC	homozygous	120283417
9	100854684	100854685	G	A	62	GENIC	homozygous	117764437
9	100857003	100857004	G	A	56	GENIC	homozygous	117620200
9	100858535	100858536	T	A	57	GENIC	homozygous	120283418
9	100860210	100860211	G	C	61	GENIC	possibly homozygous	120283419
9	100861713	100861714	G	A	29	GENIC	homozygous	120283420
9	100863695	100863696	C	T	60	GENIC	homozygous	120283421
9	100864124	100864125	T	C	45	GENIC	homozygous	117620206
9	100865863	100865864	A	G	76	GENIC	possibly homozygous	117620208
9	100867520	100867521	A	T	26	GENIC	homozygous	117400484
9	100875115	100875116	C	T	39	GENIC	homozygous	117620224
9	100875529	100875530	A	C	44	GENIC	homozygous	117620226
9	100876814	100876815	A	C	44	GENIC	possibly homozygous	120283422
9	100876818	100876819	A	C	45	GENIC	possibly homozygous	117620228
9	100878239	100878240	C	T	31	GENIC	heterozygous	117400495
9	100878674	100878675	C	T	54	GENIC	homozygous	117620230
9	100879200	100879201	T	A	51	GENIC	homozygous	117620232
9	100881759	100881760	T	C	41	GENIC	homozygous	117620234
9	100884477	100884478	G	A	42	GENIC	homozygous	117620236
9	100885091	100885092	T	C	46	GENIC	homozygous	117620238
9	100885551	100885552	G	T	55	GENIC	homozygous	117400502
9	100885856	100885857	C	T	35	GENIC	possibly homozygous	120283423
9	100886289	100886290	A	G	36	GENIC	homozygous	117620240
9	100887509	100887510	A	G	25	GENIC	homozygous	117620242
9	100887843	100887844	G	A	18	GENIC	homozygous	120283424