chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	117355168	117355169	C	T	20	GENIC	homozygous	115846989
7	117361416	117361417	G	A	13	GENIC	homozygous	115846993
7	117363624	117363625	T	C	39	GENIC	homozygous	115846995
7	117364060	117364061	C	T	24	GENIC	homozygous	115846997
7	117364954	117364955	C	T	13	GENIC	possibly homozygous	115846999
7	117365417	117365418	A	G	29	GENIC	homozygous	115847001
7	117367176	117367177	T	A	40	GENIC	homozygous	115847003
7	117368242	117368243	C	G	41	GENIC	possibly homozygous	115847005
7	117369218	117369219	T	C	17	GENIC	homozygous	115847007
7	117369343	117369344	T	G	17	GENIC	homozygous	115847009
7	117369468	117369469	G	A	24	GENIC	homozygous	115847011
7	117369487	117369488	C	T	28	GENIC	homozygous	115847013
7	117372226	117372227	T	C	20	GENIC	homozygous	115847025
7	117373159	117373160	A	G	33	GENIC	homozygous	115847027
7	117377283	117377284	G	C	35	GENIC	homozygous	115847031
7	117377925	117377926	A	G	33	GENIC	homozygous	115847033
7	117380870	117380871	A	G	24	GENIC	homozygous	115847037
7	117380871	117380872	C	T	24	GENIC	homozygous	115847039
7	117382430	117382431	T	C	28	GENIC	homozygous	115847043
7	117383180	117383181	C	T	27	GENIC	possibly homozygous	115847045
7	117383204	117383205	G	A	22	GENIC	homozygous	115847047
7	117383237	117383238	C	T	28	GENIC	homozygous	115847049
7	117383258	117383259	G	A	32	GENIC	homozygous	115847051
7	117383490	117383491	C	T	32	GENIC	possibly homozygous	115847053
7	117384333	117384334	A	G	30	GENIC	homozygous	115847055
7	117384827	117384828	C	T	20	GENIC	homozygous	115847057
7	117385028	117385029	A	T	27	GENIC	homozygous	115847059
7	117386355	117386356	A	G	22	GENIC	possibly homozygous	115847065
7	117391662	117391663	T	G	16	GENIC	homozygous	115847069
7	117393881	117393882	G	A	12	GENIC	homozygous	115847073