chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	401905	401906	G	T	35	GENIC	homozygous	110568465
18	402029	402030	A	C	35	GENIC	homozygous	110238775
18	402045	402046	T	C	40	GENIC	homozygous	110238777
18	402070	402071	A	G	36	GENIC	homozygous	110238779
18	402400	402401	C	T	24	GENIC	homozygous	110238784
18	403232	403233	A	G	9	GENIC	homozygous	110238786
18	403406	403407	A	G	27	GENIC	homozygous	110238788
18	403431	403432	C	T	25	GENIC	homozygous	110238790
18	404064	404065	T	C	38	GENIC	homozygous	110568471
18	404195	404196	A	G	36	GENIC	homozygous	110568474
18	404307	404308	G	A	29	GENIC	homozygous	110568477
18	404475	404476	T	G	34	GENIC	homozygous	110238792
18	404598	404599	T	C	33	GENIC	homozygous	110238794
18	404635	404636	G	C	31	GENIC	homozygous	110238796
18	404830	404831	T	C	10	GENIC	homozygous	110238798
18	404851	404852	T	C	8	GENIC	homozygous	110238800
18	404888	404889	C	T	4	GENIC	homozygous	110238802
18	404891	404892	G	A	4	GENIC	homozygous	110238804
18	405078	405079	G	A	6	GENIC	homozygous	110238806
18	405617	405618	G	A	14	GENIC	homozygous	110238809
18	405675	405676	C	T	18	GENIC	homozygous	110238811
18	405683	405684	A	G	18	GENIC	homozygous	110238813
18	405869	405870	A	G	21	GENIC	homozygous	110238815
18	406106	406107	T	A	34	GENIC	homozygous	110238817
18	406136	406137	T	C	27	GENIC	homozygous	110238819
18	406184	406185	C	T	31	GENIC	homozygous	110238821
18	406344	406345	G	T	32	GENIC	homozygous	110238823
18	406360	406361	G	A	27	GENIC	homozygous	110568479
18	406728	406729	A	G	43	GENIC	homozygous	110238825
18	406825	406826	A	C	31	GENIC	homozygous	110238827
18	406828	406829	G	A	28	GENIC	homozygous	110238829
18	407014	407015	A	G	26	GENIC	homozygous	110238831
18	407228	407229	T	C	21	GENIC	homozygous	110238835
18	407533	407534	C	T	2	GENIC	homozygous	110619407
18	407703	407704	C	T	24	GENIC	homozygous	110568482