chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5124775	5124776	C	T	60	GENIC	homozygous	109077074
20	5127041	5127042	T	A	34	GENIC	homozygous	109077092
20	5127630	5127631	T		31	GENIC	homozygous	129653163
20	5128383	5128384	T	C	44	GENIC	homozygous	109077100
20	5128409	5128410	G	C	47	GENIC	homozygous	109077102
20	5129526	5129527	T	G	46	GENIC	homozygous	109077111
20	5130003	5130004	T	G	44	GENIC	possibly homozygous	109420100
20	5127137	5127138	T	G	23	GENIC	homozygous	109233853
20	5129465	5129466	G	C	47	GENIC	homozygous	109233855
20	5127410	5127411	T	C	56	GENIC	homozygous	109420094
20	5127632	5127633	A	C	32	GENIC	homozygous	109420096
20	5128024	5128025	G	A	54	GENIC	homozygous	109420098
20	5127978	5127978		TT	41	GENIC	homozygous	131227935
20	5128096	5128098	AG		46	GENIC	homozygous	131227936
20	5130038	5130039	G	A	56	GENIC	homozygous	109420102
20	5132607	5132608	C	T	58	GENIC	homozygous	109420104
20	5134146	5134147	G	A	63	GENIC	homozygous	109420106
20	5134830	5134831	C	T	62	GENIC	homozygous	109420108
20	5136543	5136544	G	A	60	GENIC	homozygous	109077165
20	5137299	5137300	A	G	58	GENIC	homozygous	109420110
20	5137727	5137728	T		48	GENIC	homozygous	131227937