chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12918464	12918465	T	C	23	GENIC	homozygous	109099019
20	12918661	12918662	G	A	38	GENIC	homozygous	109492484
20	12919106	12919107	G	A	29	GENIC	homozygous	109492486
20	12920203	12920204	T	G	18	GENIC	homozygous	109099023
20	12920388	12920389	C	G	43	GENIC	homozygous	109240340
20	12920922	12920923	G	A	30	GENIC	homozygous	109527796
20	12921041	12921042	C	T	37	GENIC	homozygous	109240341
20	12922560	12922561	T	C	33	GENIC	possibly homozygous	109099025
20	12922762	12922763	A	T	38	GENIC	homozygous	109099027
20	12923503	12923504	C	T	30	GENIC	homozygous	109394080
20	12923706	12923707	G	A	40	GENIC	homozygous	109099031
20	12923990	12923991	T	C	32	GENIC	possibly homozygous	109099033
20	12924236	12924237	T	C	51	GENIC	homozygous	109099035