chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	44736650	44736651	C	T	29	GENIC	homozygous	111552944
3	44737063	44737064	C	T	36	GENIC	homozygous	111552945
3	44737272	44737273	T	C	28	GENIC	homozygous	111552946
3	44737433	44737434	G	A	19	GENIC	homozygous	111552947
3	44737453	44737454	A	G	19	GENIC	possibly homozygous	111552948
3	44737464	44737465	G	A	22	GENIC	possibly homozygous	111552949
3	44737470	44737471	C	T	19	GENIC	heterozygous	111552950
3	44737475	44737476	C	T	19	GENIC	heterozygous	111552951
3	44737478	44737479	T	C	19	GENIC	heterozygous	111552952
3	44737481	44737482	A	G	20	GENIC	heterozygous	111552953
3	44737509	44737510	T	C	23	GENIC	possibly homozygous	111552954
3	44737510	44737511	G	C	23	GENIC	possibly homozygous	111552955
3	44737516	44737517	T	C	24	GENIC	possibly homozygous	111552956
3	44737571	44737572	A	G	23	GENIC	homozygous	111552957
3	44737576	44737577	G	A	27	GENIC	possibly homozygous	111552958
3	44737616	44737617	A	G	40	GENIC	homozygous	111552959
3	44737676	44737677	G	T	26	GENIC	homozygous	111552960
3	44737722	44737723	A	T	36	GENIC	heterozygous	111552961
3	44737829	44737830	G	A	41	GENIC	possibly homozygous	111552962
3	44737832	44737833	T	C	39	GENIC	homozygous	111552963
3	44737848	44737849	C	T	37	GENIC	possibly homozygous	111552964
3	44737886	44737887	T	C	34	GENIC	homozygous	111552965
3	44737981	44737982	C	T	43	GENIC	homozygous	111552966
3	44738246	44738247	T	C	33	GENIC	homozygous	111552967
3	44738412	44738413	T	A	27	GENIC	homozygous	111552968
3	44738480	44738481	G	A	12	GENIC	homozygous	111552969
3	44738481	44738482	C	T	12	GENIC	homozygous	111552970