chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47739400	47739401	A	C	20	GENIC	possibly homozygous	49751928
13	47739623	47739624	T	C	18	GENIC	homozygous	49751929
13	47739655	47739656	T	C	18	GENIC	possibly homozygous	49751930
13	47740088	47740089	C	T	19	GENIC	possibly homozygous	49751931
13	47740313	47740314	G	A	34	GENIC	homozygous	49751932
13	47740358	47740359	A	G	20	GENIC	possibly homozygous	49751933
13	47740374	47740375	A	G	10	GENIC	homozygous	49751934
13	47740376	47740377	G	A	9	GENIC	homozygous	49751935
13	47740526	47740527	T	C	13	GENIC	homozygous	49751936
13	47740529	47740530	A	C	13	GENIC	homozygous	49751937
13	47740787	47740788	A	G	16	GENIC	possibly homozygous	49751938
13	47741003	47741004	C	T	17	GENIC	homozygous	49751940
13	47741031	47741032	T	C	17	GENIC	possibly homozygous	49751941
13	47741227	47741228	G	A	16	GENIC	homozygous	49751942
13	47741503	47741504	C	A	16	GENIC	possibly homozygous	49751943
13	47741734	47741735	G	T	30	GENIC	homozygous	49751944
13	47741902	47741903	G	A	17	GENIC	possibly homozygous	49751945
13	47742333	47742355	GTGTGTGTGTATGTGTGTGTGT	----------------------	10	GENIC	heterozygous	49751946
13	47742862	47742863	T	C	20	GENIC	possibly homozygous	49751950
13	47742872	47742873	G	A	15	GENIC	possibly homozygous	49751951
13	47742883	47742884	A	G	13	GENIC	possibly homozygous	49751952
13	47742951	47742952	G	A	20	GENIC	possibly homozygous	49751953
13	47743067	47743068	C	-	12	GENIC	homozygous	49751954
13	47743269	47743270	G	T	20	GENIC	possibly homozygous	49751955
13	47743348	47743349	A	G	17	GENIC	homozygous	49751956
13	47743355	47743356	A	C	14	GENIC	possibly homozygous	49751957