chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21104188	21104189	A	G	28	GENIC	homozygous	47329604
16	21106616	21106617	T	TC	13	GENIC	homozygous	47329616
16	21107468	21107469	C	CTTGTCATGTA	10	GENIC	homozygous	47329622
16	21106538	21106539	A	G	8	GENIC	homozygous	48181970
16	21111728	21111729	A	G	24	GENIC	homozygous	47329649
16	21112075	21112076	T	-	10	GENIC	heterozygous	48181971
16	21112921	21112922	T	A	23	GENIC	homozygous	47329653
16	21113137	21113138	G	T	25	GENIC	possibly homozygous	48181972
16	21114342	21114343	T	C	11	GENIC	homozygous	48181973
16	21116028	21116029	G	T	8	GENIC	homozygous	48181974
16	21116457	21116458	C	T	15	GENIC	homozygous	47329671
16	21116592	21116593	C	T	19	GENIC	homozygous	47329673
16	21119076	21119077	C	T	12	GENIC	homozygous	47993109
16	21119895	21119896	T	A	9	GENIC	homozygous	48181975
16	21119912	21119913	C	T	9	GENIC	homozygous	48181976
16	21123497	21123498	A	G	17	GENIC	homozygous	47329709
16	21124382	21124383	G	A	15	GENIC	homozygous	48181977
16	21124867	21124868	A	G	19	GENIC	homozygous	47329713
16	21125551	21125552	C	G	11	GENIC	homozygous	48181978
16	21126534	21126535	G	T	17	GENIC	homozygous	47329722
16	21127020	21127022	TT	--	9	GENIC	homozygous	48181979
16	21127224	21127225	A	C	21	GENIC	homozygous	47329734
16	21128489	21128490	T	A	12	GENIC	homozygous	48181980
16	21128912	21128913	C	T	9	GENIC	homozygous	47329748
16	21129590	21129591	G	A	17	GENIC	homozygous	48181981