chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37556800	37556801	G	A	62	GENIC	homozygous	51417882
10	37557313	37557314	T	TAA	20	GENIC	heterozygous	51417884
10	37557313	37557314	T	TA	20	GENIC	heterozygous	51417886
10	37557333	37557334	C	T	44	GENIC	possibly homozygous	51417888
10	37557830	37557831	C	T	59	GENIC	homozygous	51417890
10	37558491	37558492	A	T	50	GENIC	homozygous	51417892
10	37558656	37558657	G	A	39	GENIC	homozygous	51417894
10	37558672	37558673	C	T	41	GENIC	homozygous	51417896
10	37558683	37558684	G	A	37	GENIC	homozygous	51417898
10	37558706	37558707	T	G	46	GENIC	homozygous	51417900
10	37559469	37559489	ACAGTCACACACAGTCACAT	--------------------	30	GENIC	homozygous	51417902
10	37559535	37559537	AC	--	29	GENIC	homozygous	51417904
10	37559562	37559563	T	G	31	GENIC	homozygous	51417906
10	37559620	37559621	C	-	14	GENIC	heterozygous	51417908
10	37559620	37559621	C	CA	14	GENIC	heterozygous	51417910
10	37559643	37559644	C	G	20	GENIC	heterozygous	51417912
10	37559653	37559654	C	G	22	GENIC	heterozygous	51417914
10	37559919	37559920	T	-	48	GENIC	homozygous	51417916
10	37560152	37560153	C	T	71	GENIC	homozygous	51417918
10	37560280	37560285	TGGTG	-----	32	GENIC	homozygous	51417920
10	37560313	37560314	C	T	32	GENIC	homozygous	51417922
10	37560361	37560362	T	G	35	GENIC	homozygous	51417924
10	37560953	37560954	G	A	41	GENIC	homozygous	51417926
10	37561661	37561662	T	A	43	GENIC	homozygous	51417928
10	37561748	37561749	T	C	46	GENIC	homozygous	51417930
10	37561970	37561971	T	C	57	GENIC	homozygous	51417932
10	37562233	37562234	G	C	62	GENIC	homozygous	51417934
10	37566458	37566459	T	TG	8	GENIC	heterozygous	51417942
10	37564234	37564235	G	GT	71	GENIC	homozygous	51417936
10	37565311	37565315	AAAA	----	1	GENIC	homozygous	51417938
10	37565770	37565771	C	CGT	23	GENIC	possibly homozygous	51417940
10	37567660	37567661	G	GTT	10	GENIC	homozygous	51417944
10	37566458	37566459	T	TGG	8	GENIC	heterozygous	51634522