chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122207896	122207897	T		40	GENIC	homozygous	128513210
7	122207899	122207900	T	G	42	GENIC	homozygous	115860320
7	122207900	122207901	C	G	42	GENIC	homozygous	115860322
7	122209198	122209207	CCCCCCGCA		23	GENIC	homozygous	128513211
7	122209207	122209208	C	T	23	GENIC	homozygous	122851673
7	122209211	122209211		AAAGATTTAT	27	GENIC	homozygous	128513212
7	122209221	122209221		T	33	GENIC	homozygous	128513213
7	122209314	122209314		T	22	GENIC	homozygous	128513214
7	122209347	122209348	G	C	16	GENIC	homozygous	115860324
7	122209349	122209350	A	C	14	GENIC	homozygous	115860326
7	122209366	122209367	A	C	12	GENIC	homozygous	115860328
7	122209370	122209371	G	C	12	GENIC	homozygous	115860330
7	122209496	122209497	G	C	27	GENIC	homozygous	115860332
7	122209514	122209515	G	C	26	GENIC	homozygous	115860334
7	122209526	122209527	G	C	28	GENIC	homozygous	115860336
7	122224125	122224129	CATC		47	GENIC	possibly homozygous	128513215
7	122230734	122230735	C	T	76	GENIC	homozygous	115860338