chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47034220	47034221	C	T	17	GENIC	homozygous	118066586
10	47034761	47034762	A	T	12	GENIC	homozygous	116587129
10	47034997	47034998	G	A	21	GENIC	homozygous	116878167
10	47035552	47035553	T	G	21	GENIC	homozygous	116977640
10	47037307	47037308	A	T	25	GENIC	homozygous	116878169
10	47038321	47038322	C	A	28	GENIC	homozygous	116931638
10	47038446	47038447	T	C	25	GENIC	homozygous	116587131
10	47040071	47040072	A	T	27	GENIC	homozygous	116587133
10	47043065	47043066	A	T	22	GENIC	homozygous	116931640
10	47044561	47044562	G	A	23	GENIC	heterozygous	118066587
10	47044632	47044633	C	T	20	GENIC	homozygous	116931642
10	47045318	47045319	C	A	21	GENIC	homozygous	116587135
10	47045482	47045483	C	T	23	GENIC	homozygous	116931644
10	47050456	47050457	A	G	13	GENIC	homozygous	116587137
10	47051521	47051522	G	C	21	GENIC	homozygous	116587139
10	47053807	47053808	G	A	16	GENIC	homozygous	116587149
10	47054618	47054619	C	T	18	GENIC	homozygous	116878182
10	47054924	47054925	A	G	22	GENIC	homozygous	116773104
10	47055572	47055573	A	G	21	GENIC	homozygous	116587155
10	47056003	47056004	A	G	25	GENIC	homozygous	116587157
10	47057905	47057906	A	T	23	GENIC	homozygous	116587159
10	47058122	47058123	C	T	7	GENIC	homozygous	118066588
10	47058394	47058395	T	G	20	GENIC	homozygous	116878194
10	47058664	47058665	C	A	20	GENIC	homozygous	116931646
10	47058904	47058905	C	T	24	GENIC	homozygous	116931648