chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122206546	122206547	G		16	GENIC	homozygous	131433910
7	122206547	122206548	G	T	16	GENIC	homozygous	118418333
7	122207651	122207652	T	C	14	GENIC	homozygous	118418334
7	122209207	122209208	C	T	10	GENIC	homozygous	122851673
7	122209221	122209221		T	10	GENIC	homozygous	128513213
7	122207896	122207897	T		18	GENIC	homozygous	128513210
7	122209198	122209207	CCCCCCGCA		10	GENIC	homozygous	128513211
7	122209211	122209211		AAAGATTTAT	11	GENIC	homozygous	128513212
7	122207899	122207900	T	G	18	GENIC	homozygous	115860320
7	122207900	122207901	C	G	18	GENIC	homozygous	115860322
7	122209496	122209497	G	C	7	GENIC	homozygous	115860332
7	122209514	122209515	G	C	8	GENIC	homozygous	115860334
7	122209526	122209527	G	C	8	GENIC	homozygous	115860336
7	122209754	122209755	T	C	1	GENIC	homozygous	131440517
7	122212538	122212539	G	A	15	GENIC	homozygous	116225930
7	122213905	122213906	C	T	18	GENIC	homozygous	118418337
7	122214100	122214101	G	A	21	GENIC	homozygous	118418338
7	122216161	122216162	T	A	18	GENIC	homozygous	116225931
7	122217233	122217233		T	7	GENIC	homozygous	131433912
7	122220891	122220892	G	C	14	GENIC	homozygous	118418339
7	122221714	122221715	A	G	25	GENIC	homozygous	118418340
7	122222709	122222710	G	A	19	GENIC	homozygous	118418342
7	122223476	122223477	C		19	GENIC	homozygous	131433913
7	122223634	122223635	C	T	13	GENIC	homozygous	118418343
7	122223933	122223934	T	C	14	GENIC	homozygous	116225932
7	122225715	122225716	T	C	21	GENIC	homozygous	116225935
7	122227870	122227871	T	C	17	GENIC	homozygous	116225936
7	122227933	122227934	A	G	12	GENIC	homozygous	118418344
7	122229390	122229391	A	G	19	GENIC	homozygous	116225937
7	122229412	122229413	T	C	19	GENIC	homozygous	116225938
7	122229684	122229685	A	G	18	GENIC	homozygous	116225939
7	122231302	122231303	T	C	25	GENIC	homozygous	116225940
7	122217259	122217261	TT		2	GENIC	homozygous	133674696