chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	162741012	162741013	T	C	32	GENIC	homozygous	108345798
1	162742509	162742510	C	T	34	GENIC	homozygous	108345802
1	162743102	162743103	C	T	19	GENIC	homozygous	108345804
1	162743140	162743141	C	T	14	GENIC	homozygous	108345806
1	162743541	162743542	G	A	15	GENIC	homozygous	108952044
1	162746434	162746435	G	C	24	GENIC	homozygous	108345815
1	162746643	162746644	A	G	27	GENIC	homozygous	108345821
1	162747752	162747753	G	A	37	GENIC	homozygous	108345823
1	162747848	162747849	C	T	29	GENIC	homozygous	108345825
1	162748554	162748555	C	G	23	GENIC	homozygous	108345827
1	162748564	162748565	T	C	25	GENIC	homozygous	108345829
1	162749901	162749902	C	A	29	GENIC	homozygous	108345837
1	162750559	162750560	A	C	22	GENIC	homozygous	108345839
1	162751365	162751366	T	A	27	GENIC	homozygous	120487110
1	162753363	162753364	C	T	26	GENIC	homozygous	108952049
1	162753398	162753399	T	C	32	GENIC	homozygous	108345843
1	162753594	162753595	A	C	27	GENIC	homozygous	108345845
1	162753748	162753749	A	C	30	GENIC	homozygous	108345849
1	162760943	162760944	C	A	29	GENIC	homozygous	108345861
1	162761152	162761153	A	G	24	GENIC	homozygous	108345865
1	162761190	162761191	T	G	24	GENIC	homozygous	108345867
1	162762160	162762161	C	G	27	GENIC	homozygous	108345869
1	162764130	162764131	C	T	37	GENIC	homozygous	108952057
1	162764675	162764676	C	T	28	GENIC	homozygous	108345873
1	162764783	162764784	T	G	29	GENIC	homozygous	108345875
1	162765291	162765292	C	T	33	GENIC	homozygous	108345879
1	162766141	162766142	A	G	26	GENIC	homozygous	108345883