chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21047793	21047794	G	C	36	GENIC	homozygous	47329448
16	21048336	21048337	G	C	25	GENIC	homozygous	47329450
16	21049296	21049297	T	-	6	GENIC	homozygous	47882589
16	21049480	21049481	C	CCCG	10	GENIC	homozygous	47329452
16	21049919	21049920	A	G	30	GENIC	homozygous	47329454
16	21050445	21050446	A	-	12	GENIC	possibly homozygous	47329456
16	21053434	21053436	AA	--	6	GENIC	homozygous	47329458
16	21053445	21053446	A	C	6	GENIC	homozygous	47972067
16	21053758	21053759	A	ACTG	14	GENIC	homozygous	47329460
16	21053930	21053931	C	A	27	GENIC	homozygous	47329462
16	21053943	21053944	C	A	23	GENIC	homozygous	47329464
16	21055032	21055034	GG	--	16	GENIC	homozygous	47329470
16	21055358	21055359	G	GA	8	GENIC	heterozygous	47950595
16	21055359	21055360	A	-	8	GENIC	heterozygous	47329474
16	21057933	21057934	T	-	18	GENIC	possibly homozygous	47329476
16	21058277	21058278	G	A	21	GENIC	homozygous	47329478
16	21058706	21058707	C	CT	13	GENIC	heterozygous	47329480
16	21058913	21058914	C	-	28	GENIC	homozygous	47329484
16	21059561	21059563	TC	--	4	GENIC	homozygous	47999172
16	21062154	21062155	A	-	11	GENIC	homozygous	47329490
16	21064808	21064809	C	-	31	GENIC	homozygous	47329492
16	21065452	21065453	G	GA	12	GENIC	heterozygous	47329494
16	21065453	21065454	A	-	12	GENIC	heterozygous	47993047
16	21068501	21068502	C	CAA	2	GENIC	homozygous	47329496
16	21074404	21074405	G	GT	6	GENIC	homozygous	47329498