chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	104280522	104280523	T	C	19	GENIC	homozygous	113529610
14	104281061	104281062	T	C	19	GENIC	homozygous	113529612
14	104281077	104281078	G	A	29	GENIC	homozygous	113529614
14	104281222	104281223	A	C	25	GENIC	homozygous	113529616
14	104281526	104281527	C	A	22	GENIC	homozygous	113529618
14	104284593	104284594	C	T	24	GENIC	homozygous	113529620
14	104284980	104284981	A	G	35	GENIC	homozygous	113529622
14	104288943	104288944	T	C	16	GENIC	homozygous	113529626
14	104289568	104289569	G	C	19	GENIC	homozygous	113529628
14	104289586	104289587	C	T	23	GENIC	homozygous	113529630
14	104290066	104290067	T	C	18	GENIC	possibly homozygous	113529632