chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10159228	10159229	T	C	26	GENIC	homozygous	117803776
9	10160705	10160706	T	C	28	GENIC	homozygous	117244133
9	10160859	10160860	G	A	34	GENIC	homozygous	117803777
9	10161673	10161674	G	T	21	GENIC	homozygous	117803778
9	10161839	10161840	A	G	22	GENIC	homozygous	117790002
9	10162227	10162228	G	A	18	GENIC	homozygous	117803779
9	10163412	10163413	G	T	42	GENIC	homozygous	117244140
9	10163563	10163564	T	C	34	GENIC	homozygous	117244141
9	10163566	10163567	T	C	35	GENIC	homozygous	117803780
9	10164379	10164380	G	A	25	GENIC	homozygous	117803781
9	10166899	10166900	C	T	31	GENIC	heterozygous	117790006
9	10166959	10166960	T	C	59	GENIC	heterozygous	117790007
9	10168721	10168722	A	G	39	GENIC	homozygous	117803782
9	10168766	10168767	T	C	35	GENIC	homozygous	117803783
9	10168895	10168896	C	T	44	GENIC	homozygous	117803784
9	10168900	10168901	T	C	46	GENIC	homozygous	117803785
9	10169250	10169251	G	T	16	GENIC	homozygous	117803786
9	10170912	10170913	C	T	49	GENIC	homozygous	117803787
9	10171475	10171476	G	A	20	GENIC	homozygous	117244147
9	10171539	10171540	T	A	22	GENIC	homozygous	117244148
9	10172228	10172229	T	C	29	GENIC	homozygous	117244149
9	10172250	10172251	C	T	29	GENIC	homozygous	117803788
9	10173390	10173391	C	T	44	GENIC	homozygous	117803789
9	10174810	10174811	T	C	37	GENIC	homozygous	117244151
9	10175363	10175364	C	T	29	GENIC	homozygous	117803790
9	10175917	10175918	A	G	31	GENIC	homozygous	117244155
9	10176188	10176189	G	C	31	GENIC	homozygous	117803791
9	10176926	10176927	T	C	32	GENIC	homozygous	117244156
9	10181781	10181782	T	C	31	GENIC	homozygous	117244158
9	10184126	10184127	T	C	24	GENIC	homozygous	117244160
9	10184196	10184197	G	A	33	GENIC	homozygous	117803792
9	10184841	10184842	C	T	34	GENIC	homozygous	117803793