chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	135734991	135734992	T	G	31	GENIC	homozygous	56939133
4	135735084	135735085	A	G	24	GENIC	homozygous	56939134
4	135735246	135735247	A	C	25	GENIC	homozygous	56939135
4	135735588	135735589	A	G	32	GENIC	homozygous	56939136
4	135735718	135735719	A	C	18	GENIC	homozygous	56939137
4	135735729	135735730	T	G	22	GENIC	homozygous	56939138
4	135735735	135735736	T	-	17	GENIC	homozygous	56939139
4	135736298	135736299	C	T	18	GENIC	homozygous	56939140
4	135736667	135736668	G	GTTCA	16	GENIC	homozygous	56939141
4	135737462	135737463	A	G	28	GENIC	homozygous	56939142
4	135737827	135737828	A	-	10	GENIC	heterozygous	56939143
4	135739096	135739097	A	G	20	GENIC	homozygous	56939144
4	135739431	135739432	A	G	32	GENIC	homozygous	56939145
4	135739527	135739528	T	C	23	GENIC	homozygous	56939146
4	135740048	135740049	A	G	30	GENIC	homozygous	56939147
4	135742352	135742353	A	G	22	GENIC	homozygous	56939148
4	135742719	135742720	G	T	22	GENIC	homozygous	56939149
4	135742823	135742824	T	C	25	GENIC	homozygous	56939150
4	135742945	135742946	T	C	28	GENIC	homozygous	56939151
4	135745185	135745197	AGCTCCTACTAA	------------	10	GENIC	homozygous	56939152
4	135745668	135745669	C	T	14	GENIC	homozygous	56939153
4	135746059	135746060	G	GA	17	GENIC	homozygous	56939154
4	135749126	135749127	G	A	11	GENIC	homozygous	56939155
4	135749448	135749449	A	G	19	GENIC	homozygous	56939156
4	135749604	135749605	G	T	19	GENIC	homozygous	56939157
4	135751572	135751574	AT	--	18	GENIC	homozygous	56939158
4	135752014	135752015	C	T	24	GENIC	homozygous	56939159
4	135752494	135752495	C	A	31	GENIC	homozygous	56939160
4	135754695	135754696	C	T	31	GENIC	homozygous	56939161
4	135756056	135756057	T	A	14	GENIC	heterozygous	56939162
4	135758406	135758407	A	ATG	10	GENIC	homozygous	56939163
4	135758690	135758691	A	AAAAT	2	GENIC	heterozygous	56939164