chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	96051873	96051874	C	T	55	GENIC	homozygous	147253823
2	96053468	96053469	A	G	53	GENIC	homozygous	147253824
2	96053657	96053658	T	G	53	GENIC	homozygous	147253825
2	96053672	96053673	T	C	54	GENIC	homozygous	136225945
2	96053824	96053825	T		45	GENIC	possibly homozygous	135929786
2	96055334	96055335	A	G	50	GENIC	homozygous	136225948
2	96055640	96055641	C	T	56	GENIC	homozygous	136225949
2	96057312	96057313	G	A	59	GENIC	homozygous	146048227
2	96057550	96057551	G	A	60	GENIC	homozygous	136225951
2	96057773	96057774	T	C	61	GENIC	homozygous	136225952
2	96058574	96058575	A	G	34	GENIC	homozygous	136225953
2	96058666	96058667	T	G	51	GENIC	homozygous	136225954
2	96059255	96059256	A	G	57	GENIC	homozygous	136225955
2	96060348	96060349	C	T	55	GENIC	homozygous	136225957
2	96060469	96060470	C	G	51	GENIC	homozygous	136225958
2	96060584	96060585	C	G	61	GENIC	homozygous	136225959
2	96063061	96063062	G	A	57	GENIC	homozygous	136225961
2	96063560	96063561	A	T	52	GENIC	homozygous	147253826
2	96063892	96063893	C	G	49	GENIC	homozygous	147253827
2	96067191	96067192	T	G	41	GENIC	homozygous	136225966
2	96064197	96064198	G	A	56	GENIC	homozygous	147253828
2	96065800	96065801	C	T	48	GENIC	homozygous	147253829
2	96066626	96066627	G	A	49	GENIC	homozygous	147253830
2	96067749	96067750	T	A	44	GENIC	homozygous	147253831
2	96068238	96068239	A	G	41	GENIC	homozygous	136225967
2	96070648	96070649	T	C	34	GENIC	homozygous	136225971
2	96070705	96070706	G	A	45	GENIC	homozygous	136225972
2	96070833	96070833		T	46	GENIC	possibly homozygous	135929788
2	96071045	96071046	G	A	52	GENIC	homozygous	147253832
2	96071083	96071084	T	C	60	GENIC	homozygous	136225974
2	96071325	96071326	C	T	47	GENIC	homozygous	136225975