chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	2587365	2587366	A	C	18	GENIC	possibly homozygous	111698332
16	2589362	2589363	C		20	GENIC	homozygous	129326836
16	2589369	2589370	C		20	GENIC	homozygous	129326837
16	2589380	2589381	C		17	GENIC	homozygous	129326838
16	2589389	2589390	C		17	GENIC	homozygous	129326839
16	2589402	2589403	C		13	GENIC	homozygous	129326840
16	2589425	2589426	C	T	14	GENIC	homozygous	111921278
16	2589441	2589442	C	T	14	GENIC	homozygous	111921280
16	2589488	2589489	C	T	17	GENIC	homozygous	111698334
16	2589491	2589492	C	T	18	GENIC	homozygous	111698336
16	2589497	2589497		T	18	GENIC	homozygous	129326841
16	2589498	2589499	C	T	20	GENIC	homozygous	111698338
16	2589501	2589502	C	T	21	GENIC	homozygous	111698340
16	2589507	2589507		A	21	GENIC	homozygous	129326842
16	2589512	2589513	C	A	21	GENIC	homozygous	111698342
16	2589515	2589516	C	A	21	GENIC	homozygous	111698344
16	2589515	2589515		A	21	GENIC	homozygous	129326843
16	2589524	2589525	C		23	GENIC	homozygous	129326844
16	2589535	2589536	T	C	22	GENIC	homozygous	111698346
16	2592553	2592553		A	10	GENIC	homozygous	129326845
16	2592563	2592564	T	C	11	GENIC	homozygous	111921282
16	2592564	2592565	C	A	11	GENIC	homozygous	111921284
16	2592566	2592566		A	11	GENIC	homozygous	129326846
16	2592583	2592583		A	13	GENIC	homozygous	129326847
16	2592588	2592589	G	A	12	GENIC	homozygous	111921286
16	2592598	2592599	G	A	13	GENIC	homozygous	111921288