chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	144942587	144942588	C	T	34	GENIC	homozygous	115946160
7	144944071	144944072	C	T	11	GENIC	homozygous	115946162
7	144944613	144944614	C	T	23	GENIC	homozygous	115946163
7	144944617	144944618	C	T	21	GENIC	homozygous	115946165
7	144944663	144944664	A	G	19	GENIC	homozygous	115946167
7	144944913	144944914	G	A	23	GENIC	homozygous	115946169
7	144945531	144945532	G	T	17	GENIC	homozygous	115946171
7	144945850	144945851	C	T	17	GENIC	homozygous	115946175
7	144953382	144953383	C	T	21	GENIC	homozygous	115946189
7	144953638	144953639	C	A	23	GENIC	homozygous	115946191
7	144954095	144954096	G	A	22	GENIC	homozygous	115946193
7	144955952	144955953	C	T	16	GENIC	homozygous	115946197
7	144958429	144958430	C	T	19	GENIC	homozygous	115946199
7	144961041	144961042	A	G	11	GENIC	homozygous	115946205
7	144964293	144964294	T	C	16	GENIC	homozygous	115946209
7	144964894	144964895	C	T	12	GENIC	homozygous	115946211
7	144965636	144965637	C	G	16	GENIC	homozygous	115946213