chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5448799	5448800	G	A	26	GENIC	homozygous	109077996
20	5450404	5450405	C	A	25	GENIC	homozygous	109077998
20	5450473	5450474	T	C	33	GENIC	possibly homozygous	109234051
20	5450833	5450834	G	C	39	GENIC	homozygous	109078000
20	5450982	5450983	C	G	40	GENIC	heterozygous	109420400
20	5450985	5450986	G	C	41	GENIC	heterozygous	109420402
20	5450986	5450987	G	A	41	GENIC	heterozygous	109420404
20	5450990	5450991	T	A	42	GENIC	heterozygous	109420406
20	5451044	5451045	G	C	38	GENIC	homozygous	109078002
20	5452122	5452123	A	G	35	GENIC	homozygous	109078008
20	5452571	5452572	G	A	31	GENIC	homozygous	109234052
20	5453607	5453608	A	G	16	GENIC	homozygous	109078010
20	5453658	5453659	C	T	30	GENIC	homozygous	109234053
20	5453690	5453691	A	G	31	GENIC	homozygous	109078012
20	5453850	5453851	T	C	39	GENIC	homozygous	109078014
20	5455065	5455066	A	G	18	GENIC	homozygous	109234054
20	5455171	5455172	G	A	28	GENIC	homozygous	109234055
20	5455320	5455321	G	A	15	GENIC	homozygous	109234056
20	5455619	5455620	T	C	12	GENIC	homozygous	109078038