chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160394685	160394686	G	A	44	GENIC	homozygous	114074195
5	160394781	160394782	T	C	44	GENIC	homozygous	114074196
5	160395004	160395005	T	C	47	GENIC	homozygous	114074197
5	160395013	160395014	C	T	51	GENIC	homozygous	114074198
5	160395804	160395805	C	T	56	GENIC	homozygous	114074199
5	160395890	160395891	C	G	47	GENIC	homozygous	114074200
5	160395896	160395897	T	C	50	GENIC	homozygous	114074201
5	160396095	160396096	A	G	29	GENIC	possibly homozygous	114074202
5	160396109	160396110	G	A	27	GENIC	possibly homozygous	114074203
5	160396143	160396144	A	C	18	GENIC	homozygous	114074204
5	160396145	160396146	G	A	19	GENIC	homozygous	114074205
5	160396166	160396167	C	T	16	GENIC	possibly homozygous	114074206
5	160396506	160396507	A	C	50	GENIC	homozygous	114074207
5	160396734	160396735	A	G	23	GENIC	heterozygous	114074208
5	160396961	160396962	T	C	62	GENIC	homozygous	114074209
5	160397071	160397072	G	A	57	GENIC	homozygous	114074210
5	160398250	160398251	A	G	60	GENIC	homozygous	114074211
5	160398632	160398633	T	C	43	GENIC	possibly homozygous	114074212
5	160398679	160398680	C	G	51	GENIC	heterozygous	114074213
5	160399256	160399257	T	A	8	GENIC	homozygous	114074214
5	160399800	160399801	C	T	50	GENIC	homozygous	114074215
5	160401780	160401781	A	C	19	GENIC	homozygous	114074216
5	160401873	160401874	A	G	38	GENIC	homozygous	114074217