chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	44524268	44524269	A	T	18	GENIC	homozygous	126109546
13	44524345	44524346	T	C	19	GENIC	homozygous	126109547
13	44525870	44525871	A	G	16	GENIC	homozygous	126109548
13	44528715	44528716	C	T	14	GENIC	homozygous	126109549
13	44529170	44529171	G	A	18	GENIC	homozygous	126109550
13	44530702	44530703	G	A	14	GENIC	homozygous	126109551
13	44531377	44531378	A	G	16	GENIC	homozygous	126109552
13	44532363	44532364	C	T	25	GENIC	homozygous	126109553
13	44534379	44534380	A	G	9	GENIC	homozygous	126109554
13	44535770	44535771	T	A	11	GENIC	homozygous	126109555
13	44536602	44536603	A	G	18	GENIC	homozygous	126109556
13	44536628	44536629	A	G	19	GENIC	homozygous	126109557
13	44536670	44536671	A	G	10	GENIC	homozygous	126109558
13	44536913	44536914	T	C	21	GENIC	homozygous	126109559
13	44536963	44536964	C	T	18	GENIC	homozygous	126109560
13	44536976	44536977	T	G	11	GENIC	homozygous	126109561
13	44537551	44537552	C	T	10	GENIC	homozygous	126065647
13	44539694	44539695	T	A	10	GENIC	homozygous	126109562
13	44540847	44540848	C	T	17	GENIC	homozygous	126109563
13	44543690	44543691	C	T	5	GENIC	homozygous	126109564
13	44545435	44545436	A	T	18	GENIC	homozygous	126109565
13	44546004	44546005	C	G	13	GENIC	heterozygous	126065649
13	44546094	44546095	T	C	8	GENIC	homozygous	126065650
13	44549324	44549325	G	A	16	GENIC	homozygous	126109566
13	44550006	44550007	T	C	19	GENIC	homozygous	126109567
13	44550007	44550008	T	C	19	GENIC	homozygous	126109568
13	44550108	44550109	C	G	22	GENIC	homozygous	126109569
13	44550613	44550614	G	C	28	GENIC	homozygous	126065651
13	44550785	44550786	A	T	10	GENIC	homozygous	126109570
13	44550892	44550893	G	A	7	GENIC	heterozygous	126109571
13	44552583	44552584	C	A	25	GENIC	homozygous	126109572
13	44553178	44553179	C	A	20	GENIC	homozygous	126109573