chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	29385343	29385344	G	T	36	GENIC	homozygous	54561142
7	29385559	29385560	T	A	41	GENIC	homozygous	53853912
7	29385870	29385871	T	A	39	GENIC	homozygous	53853913
7	29385998	29385999	A	G	35	GENIC	homozygous	53853915
7	29386291	29386292	A	ACC	19	GENIC	possibly homozygous	53853916
7	29386291	29386292	A	AC	19	GENIC	heterozygous	53853917
7	29387580	29387581	C	T	38	GENIC	possibly homozygous	54561144
7	29387754	29387755	A	ATT	18	GENIC	homozygous	54561146
7	29389060	29389061	A	T	39	GENIC	homozygous	53853925
7	29390499	29390500	G	GT	31	GENIC	homozygous	54561148
7	29390739	29390740	T	C	44	GENIC	possibly homozygous	53853934
7	29391500	29391501	C	T	50	GENIC	homozygous	54561150
7	29391593	29391594	G	GC	38	GENIC	homozygous	53853936
7	29392158	29392159	G	GT	23	GENIC	possibly homozygous	53853940
7	29392159	29392160	G	T	35	GENIC	heterozygous	53853941
7	29392160	29392161	G	GGTTGCGGGCA	22	GENIC	homozygous	53853942
7	29392296	29392297	G	T	32	GENIC	possibly homozygous	53853943
7	29392538	29392540	TT	--	20	GENIC	homozygous	53853946
7	29392748	29392749	C	T	35	GENIC	homozygous	53853947
7	29393034	29393042	CTAGGCTA	--------	17	GENIC	homozygous	54561152
7	29393492	29393493	C	T	13	GENIC	homozygous	54561155
7	29393689	29393690	C	G	23	GENIC	heterozygous	53853955
7	29393993	29393994	C	CA	30	GENIC	homozygous	54561157
7	29394789	29394790	C	T	18	GENIC	homozygous	53853958
7	29395200	29395201	T	G	52	GENIC	homozygous	53853961
7	29388112	29388113	C	T	39	GENIC	heterozygous	54819734
7	29390173	29390174	C	T	42	GENIC	homozygous	54819736
7	29391604	29391606	GT	--	4	GENIC	heterozygous	54189019
7	29393685	29393686	C	G	23	GENIC	heterozygous	54189020