chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	140222794	140222795	T	C	21	GENIC	heterozygous	69178729
7	140222806	140222807	T	C	20	GENIC	heterozygous	69178730
7	140222833	140222834	A	G	23	GENIC	homozygous	69178731
7	140223570	140223571	A	G	7	GENIC	homozygous	69178733
7	140223615	140223616	C	T	14	GENIC	homozygous	69388196
7	140223642	140223643	C	T	21	GENIC	heterozygous	69178734
7	140223648	140223649	T	A	21	GENIC	heterozygous	69178735
7	140224339	140224340	C	T	13	GENIC	homozygous	69178736
7	140224801	140224802	T	C	11	GENIC	homozygous	69178737
7	140224940	140224941	T	A	17	GENIC	homozygous	69178739
7	140225035	140225036	G	A	17	GENIC	homozygous	69178740
7	140225370	140225371	G	C	13	GENIC	heterozygous	69388197
7	140225383	140225384	C	G	11	GENIC	homozygous	69178742
7	140225588	140225589	T	C	37	GENIC	homozygous	69178743
7	140225994	140225995	C	A	28	GENIC	heterozygous	69178744
7	140227280	140227281	G	C	18	GENIC	possibly homozygous	69178745
7	140227647	140227648	A	G	12	GENIC	heterozygous	81975699