chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47453551	47453552	C	T	10	GENIC	homozygous	114668591
13	47456371	47456372	C	T	36	GENIC	homozygous	114668593
13	47456739	47456740	T	G	33	GENIC	homozygous	114614722
13	47456740	47456741	T	A	34	GENIC	homozygous	114614723
13	47456752	47456753	C	T	34	GENIC	homozygous	114668595
13	47457070	47457071	A	C	34	GENIC	homozygous	114668597
13	47457766	47457767	G	C	32	GENIC	homozygous	114614724
13	47457991	47457992	T	A	23	GENIC	homozygous	114668599
13	47458280	47458281	C	T	32	GENIC	homozygous	114668601
13	47459764	47459765	T	C	31	GENIC	homozygous	114614725
13	47459829	47459830	C	T	19	GENIC	homozygous	114668603
13	47460306	47460307	T	C	18	GENIC	homozygous	114668605
13	47461808	47461809	T	C	17	GENIC	homozygous	114668609
13	47462191	47462192	A	C	15	GENIC	homozygous	114668611
13	47462193	47462194	G	A	16	GENIC	homozygous	114614726
13	47462760	47462761	G	A	14	GENIC	homozygous	114668613
13	47462840	47462841	C	T	20	GENIC	homozygous	114668615
13	47463182	47463183	C	T	20	GENIC	homozygous	114668617
13	47463514	47463515	C	T	29	GENIC	homozygous	114668619
13	47463982	47463983	C	T	24	GENIC	homozygous	114668621
13	47464191	47464192	A	G	17	GENIC	homozygous	114614727
13	47464517	47464518	G	T	24	GENIC	homozygous	114614728
13	47464652	47464653	C	T	29	GENIC	homozygous	114614729
13	47466184	47466185	A	T	21	GENIC	homozygous	114668623
13	47466484	47466485	C	T	17	GENIC	homozygous	114668625