chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21048685	21048686	T	TTTTTG	16	GENIC	homozygous	47741285
16	21049010	21049011	T	TCACACACA	18	GENIC	homozygous	47741289
16	21049296	21049297	T	-	11	GENIC	homozygous	47882589
16	21049480	21049481	C	CCCG	10	GENIC	homozygous	47329452
16	21050445	21050446	A	-	22	GENIC	possibly homozygous	47329456
16	21051271	21051272	G	T	29	GENIC	homozygous	47741291
16	21053435	21053436	A	-	29	GENIC	homozygous	47741293
16	21053758	21053759	A	ACTG	39	GENIC	homozygous	47329460
16	21055032	21055034	GG	--	20	GENIC	possibly homozygous	47329470
16	21055358	21055359	G	GA	10	GENIC	heterozygous	47950595
16	21055359	21055360	A	-	10	GENIC	heterozygous	47329474
16	21058706	21058707	C	CT	28	GENIC	possibly homozygous	47329480
16	21058805	21058806	C	CT	20	GENIC	heterozygous	47627458
16	21058913	21058914	C	-	22	GENIC	homozygous	47329484
16	21062153	21062154	G	GA	11	GENIC	heterozygous	47924427
16	21062154	21062155	A	-	11	GENIC	heterozygous	47329490
16	21062288	21062289	C	T	20	GENIC	homozygous	47741295
16	21068501	21068502	C	CAA	5	GENIC	heterozygous	47329496
16	21074404	21074405	G	GT	24	GENIC	possibly homozygous	47329498