chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	117040660	117040661	G	A	17	GENIC	homozygous	57619133
3	117040898	117040899	A	T	6	GENIC	homozygous	57619135
3	117040915	117040916	T	A	2	GENIC	homozygous	57619137
3	117040918	117040919	G	T	1	GENIC	homozygous	57619139
3	117043799	117043800	C	-	9	GENIC	heterozygous	58178068
3	117044329	117044330	C	-	2	GENIC	homozygous	57619169
3	117044375	117044376	T	C	1	GENIC	homozygous	58178070
3	117045634	117045635	A	T	10	GENIC	possibly homozygous	58178072
3	117045840	117045841	G	A	19	GENIC	homozygous	58178074
3	117046378	117046379	T	C	14	GENIC	possibly homozygous	58009087
3	117046621	117046622	C	T	18	GENIC	possibly homozygous	57619171
3	117046737	117046738	T	C	12	GENIC	homozygous	58009090
3	117047987	117047988	G	T	23	GENIC	possibly homozygous	58178076
3	117050638	117050639	G	A	16	GENIC	heterozygous	58009101
3	117051087	117051088	A	T	18	GENIC	homozygous	58009104
3	117051484	117051485	G	A	11	GENIC	heterozygous	57619176
3	117052758	117052759	A	G	18	GENIC	possibly homozygous	58009109
3	117053965	117053966	C	G	16	GENIC	possibly homozygous	57619178
3	117055777	117055778	G	A	20	GENIC	homozygous	58178080
3	117055825	117055826	G	C	19	GENIC	homozygous	58009115
3	117056117	117056118	G	C	23	GENIC	homozygous	58009121
3	117057521	117057522	C	T	19	GENIC	possibly homozygous	58178082
3	117057850	117057851	T	C	7	GENIC	possibly homozygous	58009127