chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37557057	37557058	C	T	31	GENIC	homozygous	51849801
10	37557314	37557316	AA	--	16	GENIC	homozygous	51849804
10	37557333	37557334	C	T	24	GENIC	homozygous	51417888
10	37558475	37558476	C	T	26	GENIC	homozygous	51849807
10	37559000	37559001	C	T	21	GENIC	homozygous	51849810
10	37559316	37559317	T	C	38	GENIC	homozygous	51849812
10	37559535	37559537	AC	--	27	GENIC	homozygous	51417904
10	37559620	37559621	C	-	24	GENIC	heterozygous	51417908
10	37559620	37559621	C	CA	24	GENIC	heterozygous	51417910
10	37560054	37560055	A	G	21	GENIC	homozygous	51849815
10	37560361	37560362	T	G	16	GENIC	homozygous	51417924
10	37561579	37561580	C	T	35	GENIC	homozygous	51849818
10	37561748	37561749	T	C	29	GENIC	homozygous	51417930
10	37561970	37561971	T	C	36	GENIC	homozygous	51417932
10	37562233	37562234	G	C	36	GENIC	homozygous	51417934
10	37562531	37562532	G	GCCTGAGCATC	13	GENIC	homozygous	51849821
10	37564234	37564235	G	GT	13	GENIC	homozygous	51417936
10	37566172	37566173	C	T	22	GENIC	homozygous	51849825
10	37566264	37566266	CC	--	12	GENIC	homozygous	51849828
10	37566527	37566528	T	C	24	GENIC	homozygous	51849831
10	37568127	37568128	C	T	31	GENIC	homozygous	51849834
10	37566277	37566278	C	A	27	GENIC	possibly homozygous	51984941