chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	16866358	16866359	G	C	25	GENIC	homozygous	117269806
9	16866526	16866527	T	A	42	GENIC	homozygous	117269807
9	16866861	16866862	A	G	24	GENIC	homozygous	117269809
9	16867216	16867217	C	A	37	GENIC	homozygous	117269810
9	16867698	16867699	G	A	15	GENIC	homozygous	117269812
9	16868233	16868234	C	T	40	GENIC	homozygous	117269813
9	16872237	16872238	C	T	37	GENIC	homozygous	117269814
9	16872782	16872783	C	A	62	GENIC	homozygous	117269815
9	16874550	16874551	T	C	50	GENIC	homozygous	117269816
9	16874912	16874913	C	T	59	GENIC	homozygous	117269817
9	16875120	16875121	T	C	30	GENIC	homozygous	117269818
9	16877866	16877867	C	G	49	GENIC	homozygous	117269819
9	16877890	16877891	A	G	47	GENIC	homozygous	117269820
9	16880667	16880668	C	G	40	GENIC	homozygous	117462488
9	16882638	16882639	A	G	39	GENIC	homozygous	117269822
9	16884995	16884996	G	A	36	GENIC	homozygous	117269823
9	16885839	16885840	T	C	22	GENIC	possibly homozygous	117269824
9	16885842	16885843	G	A	23	GENIC	possibly homozygous	117269825
9	16886161	16886162	T	C	50	GENIC	homozygous	117269826
9	16891731	16891732	G	A	26	GENIC	homozygous	117269827
9	16897331	16897332	C	T	31	GENIC	homozygous	117269829
9	16897646	16897647	C	T	41	GENIC	homozygous	117269830
9	16899009	16899010	C	T	17	GENIC	homozygous	117269831