chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130396062	130396063	T	G	44	GENIC	homozygous	115890102
7	130396596	130396597	A	C	54	GENIC	homozygous	115890104
7	130396890	130396898	TTCATGTG		50	GENIC	homozygous	128520307
7	130397005	130397006	A	G	43	GENIC	homozygous	115890106
7	130397241	130397242	T	A	51	GENIC	homozygous	115890110
7	130397283	130397284	G	A	51	GENIC	homozygous	115890112
7	130398928	130398930	GT		40	GENIC	homozygous	128520308
7	130402216	130402217	T	C	52	GENIC	homozygous	115890118
7	130400135	130400136	G	A	52	GENIC	homozygous	115890114
7	130402213	130402214	C	T	53	GENIC	homozygous	115890116
7	130403077	130403078	A	T	47	GENIC	homozygous	115890120
7	130403512	130403513	C	T	56	GENIC	homozygous	115890122