chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	122814567	122814568	C	T	32	GENIC	homozygous	116691789
8	122814606	122814607	A	G	33	GENIC	homozygous	116691791
8	122815009	122815010	G	A	27	GENIC	homozygous	116691793
8	122815113	122815114	G	A	22	GENIC	homozygous	116691795
8	122815954	122815955	G	A	16	GENIC	homozygous	116691797
8	122816266	122816267	C	T	29	GENIC	homozygous	116691799
8	122816525	122816526	T	C	24	GENIC	homozygous	116691801
8	122816707	122816708	A	G	12	GENIC	homozygous	116691803
8	122817407	122817408	C	T	33	GENIC	homozygous	116691805
8	122818122	122818123	T	C	14	GENIC	homozygous	116691809
8	122818945	122818946	G	C	26	GENIC	homozygous	116691811
8	122821353	122821354	C	A	25	GENIC	homozygous	116691817
8	122824327	122824328	T	A	30	GENIC	homozygous	116691819
8	122825482	122825483	A	G	19	GENIC	homozygous	116691823
8	122826235	122826236	G	A	22	GENIC	homozygous	116691825
8	122826258	122826259	G	A	27	GENIC	homozygous	116691827
8	122831533	122831534	G	A	24	GENIC	homozygous	116691831
8	122831599	122831600	C	T	30	GENIC	homozygous	116691833
8	122832344	122832345	T	C	10	GENIC	homozygous	116691835
8	122832399	122832400	C	T	22	GENIC	homozygous	116691837
8	122834667	122834668	A	G	18	GENIC	homozygous	116691839
8	122834734	122834735	A	G	34	GENIC	homozygous	116691841
8	122837179	122837180	G	C	20	GENIC	homozygous	116691843
8	122839358	122839359	A	G	29	GENIC	possibly homozygous	116691845
8	122840218	122840219	G	A	17	GENIC	homozygous	116691857
8	122839486	122839487	G	C	22	GENIC	homozygous	116691847
8	122839918	122839919	C	T	26	GENIC	homozygous	116691851
8	122840136	122840137	T	A	21	GENIC	homozygous	116691853
8	122840178	122840179	A	G	17	GENIC	homozygous	116691855
8	122840277	122840278	A	C	16	GENIC	homozygous	116691859
8	122840756	122840757	A	T	13	GENIC	homozygous	116691861
8	122840765	122840766	G	T	9	GENIC	homozygous	116691863
8	122840994	122840995	C	G	12	GENIC	homozygous	116691865
8	122840995	122840996	A	G	12	GENIC	homozygous	116691867
8	122841008	122841009	C	G	11	GENIC	homozygous	116691869