chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122204909	122204910	G	A	29	GENIC	homozygous	116225921
7	122205070	122205071	T	A	21	GENIC	homozygous	116225922
7	122205357	122205358	A	G	25	GENIC	homozygous	116225923
7	122205845	122205846	T	C	18	GENIC	homozygous	116225924
7	122206392	122206393	G	A	17	GENIC	homozygous	116225925
7	122206413	122206414	G	A	14	GENIC	homozygous	116225926
7	122207899	122207900	T	G	15	GENIC	homozygous	115860320
7	122207900	122207901	C	G	15	GENIC	homozygous	115860322
7	122208086	122208087	T	C	28	GENIC	homozygous	116225927
7	122209496	122209497	G	C	11	GENIC	homozygous	115860332
7	122209514	122209515	G	C	10	GENIC	homozygous	115860334
7	122209526	122209527	G	C	11	GENIC	homozygous	115860336
7	122212538	122212539	G	A	24	GENIC	homozygous	116225930
7	122216161	122216162	T	A	17	GENIC	homozygous	116225931
7	122223933	122223934	T	C	21	GENIC	homozygous	116225932
7	122224644	122224645	C	T	33	GENIC	homozygous	116225933
7	122225043	122225044	G	A	26	GENIC	homozygous	116225934
7	122225715	122225716	T	C	25	GENIC	homozygous	116225935
7	122229390	122229391	A	G	36	GENIC	homozygous	116225937
7	122229412	122229413	T	C	29	GENIC	homozygous	116225938
7	122229684	122229685	A	G	24	GENIC	homozygous	116225939
7	122231302	122231303	T	C	30	GENIC	homozygous	116225940