chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	219971103	219971104	C	T	35	GENIC	heterozygous	108994091
1	219971114	219971115	T	G	34	GENIC	heterozygous	108542019
1	219971327	219971328	C	T	21	GENIC	homozygous	108542021
1	219971328	219971329	A	G	21	GENIC	homozygous	108542023
1	219980924	219980925	T	C	27	GENIC	homozygous	108994092
1	219986129	219986130	C	T	23	GENIC	heterozygous	108994093
1	219986133	219986134	C	T	24	GENIC	heterozygous	108994094
1	219990376	219990377	C	T	23	GENIC	homozygous	108542048
1	219991660	219991661	C	T	18	GENIC	homozygous	108542050
1	219991700	219991701	A	G	21	GENIC	homozygous	108542052
1	219994005	219994006	C	T	30	GENIC	homozygous	108542054
1	219994143	219994144	T	C	29	GENIC	homozygous	108542056
1	219994428	219994429	A	G	20	GENIC	homozygous	108542058
1	219994528	219994529	T	A	19	GENIC	homozygous	108542060
1	219994728	219994729	C	T	23	GENIC	homozygous	108542062
1	219995509	219995510	C	T	37	GENIC	homozygous	108542064
1	219995980	219995981	A	G	22	GENIC	homozygous	108542066
1	219996213	219996214	A	G	15	GENIC	homozygous	108542068
1	219996288	219996289	T	A	21	GENIC	homozygous	108542070
1	219996375	219996376	T	C	20	GENIC	homozygous	108542072
1	219996482	219996483	A	G	12	GENIC	possibly homozygous	108542077
1	219996934	219996935	T	C	16	GENIC	homozygous	108542079
1	219997058	219997059	G	A	23	GENIC	homozygous	108542081
1	219997867	219997868	A	G	13	GENIC	homozygous	108542083
1	219998528	219998529	T	C	16	GENIC	homozygous	108542085
1	219999881	219999882	G	A	32	GENIC	homozygous	108542087
1	220000709	220000710	G	A	20	GENIC	possibly homozygous	108542089