chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37557057	37557058	C	T	28	GENIC	homozygous	51849801
10	37557314	37557316	AA	--	17	GENIC	possibly homozygous	51849804
10	37557333	37557334	C	T	23	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	35	GENIC	homozygous	51849812
10	37559535	37559537	AC	--	26	GENIC	homozygous	51417904
10	37560054	37560055	A	G	20	GENIC	homozygous	51849815
10	37560361	37560362	T	G	15	GENIC	homozygous	51417924
10	37561579	37561580	C	T	34	GENIC	homozygous	51849818
10	37562531	37562532	G	GCCTGAGCATC	22	GENIC	homozygous	51849821
10	37564234	37564235	G	GT	12	GENIC	homozygous	51417936
10	37561748	37561749	T	C	28	GENIC	homozygous	51417930
10	37561970	37561971	T	C	36	GENIC	homozygous	51417932
10	37562233	37562234	G	C	36	GENIC	homozygous	51417934
10	37566171	37566172	A	ATGTGTGTGTGTGTGTGTGTG	4	GENIC	homozygous	52493886
10	37566264	37566266	CC	--	13	GENIC	homozygous	51849828
10	37566527	37566528	T	C	19	GENIC	homozygous	51849831
10	37568127	37568128	C	T	31	GENIC	homozygous	51849834