chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	18445469	18445470	C	G	36	GENIC	homozygous	115587183
7	18446479	18446480	T	C	42	GENIC	possibly homozygous	115587184
7	18451547	18451548	T	C	49	GENIC	homozygous	115587185
7	18454670	18454671	G	A	70	GENIC	homozygous	115587186
7	18456106	18456107	T	A	56	GENIC	homozygous	115587187
7	18458163	18458164	A	G	53	GENIC	homozygous	115587188
7	18459893	18459894	A	G	41	GENIC	homozygous	115587189
7	18463135	18463136	C	T	44	GENIC	homozygous	115587190
7	18464530	18464531	C	T	47	GENIC	homozygous	115587191
7	18468215	18468216	G	A	56	GENIC	homozygous	115587192
7	18472383	18472384	A	T	41	GENIC	homozygous	115587193
7	18473432	18473433	G	A	55	GENIC	homozygous	115587194
7	18474332	18474333	C	T	81	GENIC	homozygous	115587195
7	18474671	18474672	T	C	56	GENIC	homozygous	115587196
7	18481232	18481233	T	A	62	GENIC	homozygous	115587197
7	18482177	18482178	C	T	49	GENIC	possibly homozygous	115587198
7	18482853	18482854	G	A	57	GENIC	possibly homozygous	115587199
7	18487458	18487459	T	C	69	GENIC	heterozygous	116007932
7	18487470	18487471	A	C	82	GENIC	heterozygous	115587200
7	18487494	18487495	A	T	94	GENIC	heterozygous	116007933
7	18487704	18487705	T	A	53	GENIC	homozygous	115587201
7	18489814	18489815	A	G	48	GENIC	homozygous	115587202