chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5448799	5448800	G	A	25	GENIC	homozygous	109077996
20	5450404	5450405	C	A	19	GENIC	homozygous	109077998
20	5450833	5450834	G	C	12	GENIC	homozygous	109078000
20	5451044	5451045	G	C	26	GENIC	homozygous	109078002
20	5451408	5451409	C	T	13	GENIC	homozygous	109078004
20	5451520	5451521	T	C	17	GENIC	homozygous	109078006
20	5452122	5452123	A	G	6	GENIC	homozygous	109078008
20	5452999	5453000	C	T	7	GENIC	homozygous	119835988
20	5453103	5453104	A	G	5	GENIC	homozygous	119835989
20	5453291	5453292	T	C	21	GENIC	homozygous	119835991
20	5453292	5453293	G	A	21	GENIC	homozygous	124628365
20	5453690	5453691	A	G	13	GENIC	homozygous	109078012
20	5453856	5453857	G	A	7	GENIC	homozygous	109078016
20	5454019	5454020	T	C	4	GENIC	heterozygous	109078018
20	5454030	5454031	G	T	6	GENIC	heterozygous	109078022
20	5454060	5454061	A	G	15	GENIC	homozygous	109078024
20	5454121	5454122	C	T	12	GENIC	homozygous	109078026
20	5454206	5454207	T	C	11	GENIC	homozygous	109078028
20	5454211	5454212	C	T	11	GENIC	homozygous	109078030
20	5455019	5455020	A	G	7	GENIC	homozygous	109078032
20	5455349	5455350	C	T	7	GENIC	homozygous	109078034
20	5455619	5455620	T	C	16	GENIC	homozygous	109078038