chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21047946	21047947	T	C	9	GENIC	homozygous	47993037
16	21049011	21049013	CA	--	13	GENIC	homozygous	47993038
16	21049296	21049297	T	-	13	GENIC	possibly homozygous	47882589
16	21049480	21049481	C	CCCG	5	GENIC	homozygous	47329452
16	21049792	21049793	A	G	19	GENIC	homozygous	47993040
16	21050445	21050446	A	-	9	GENIC	heterozygous	47329456
16	21050577	21050578	C	T	10	GENIC	homozygous	47993041
16	21053435	21053436	A	-	13	GENIC	homozygous	47741293
16	21053758	21053759	A	ACTG	19	GENIC	homozygous	47329460
16	21054827	21054828	C	T	18	GENIC	homozygous	47993042
16	21055359	21055360	A	-	7	GENIC	heterozygous	47329474
16	21058706	21058707	C	CT	6	GENIC	heterozygous	47329480
16	21058913	21058914	C	-	22	GENIC	homozygous	47329484
16	21059557	21059558	T	TC	5	GENIC	heterozygous	47993043
16	21059562	21059563	C	T	8	GENIC	homozygous	47993044
16	21064345	21064346	C	CGCCTGGGCCTGG	6	GENIC	homozygous	47993045
16	21064607	21064608	G	C	9	GENIC	homozygous	47993046
16	21065453	21065454	A	-	7	GENIC	homozygous	47993047
16	21066259	21066260	C	T	26	GENIC	homozygous	47993048
16	21072973	21072974	T	C	6	GENIC	homozygous	47993049
16	21073141	21073142	G	A	15	GENIC	homozygous	47993050
16	21074138	21074139	G	A	7	GENIC	homozygous	47993051
16	21074405	21074406	T	G	14	GENIC	homozygous	47993053
16	21074418	21074421	TTT	---	15	GENIC	homozygous	47993054
16	21075460	21075461	G	A	25	GENIC	homozygous	47993055
16	21075489	21075490	C	T	26	GENIC	homozygous	47993056
16	21078054	21078055	G	A	23	GENIC	homozygous	47993057
16	21058805	21058806	C	CT	6	GENIC	heterozygous	47627458
16	21062153	21062154	G	GA	5	GENIC	heterozygous	47924427