chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	25339515	25339516	T	C	42	GENIC	homozygous	113695192
5	25339712	25339713	A	G	76	GENIC	homozygous	113695194
5	25340581	25340582	G	T	44	GENIC	homozygous	113695196
5	25340839	25340840	T	C	44	GENIC	homozygous	113695202
5	25342564	25342565	C	T	48	GENIC	homozygous	113695204
5	25342613	25342614	G	A	66	GENIC	homozygous	113695206
5	25342729	25342730	T	C	54	GENIC	possibly homozygous	113695208
5	25342732	25342733	G	A	56	GENIC	homozygous	113695210
5	25345151	25345152	G	T	46	GENIC	homozygous	113695212
5	25345231	25345232	A	G	54	GENIC	homozygous	113695214
5	25346326	25346327	C	T	48	GENIC	possibly homozygous	114110080
5	25346872	25346873	T	A	20	GENIC	homozygous	113695216
5	25346879	25346880	C	A	23	GENIC	homozygous	113695218
5	25346914	25346915	A	G	38	GENIC	homozygous	113695220
5	25347714	25347715	A	C	46	GENIC	homozygous	113695222
5	25347793	25347794	C	T	52	GENIC	possibly homozygous	113695224
5	25348037	25348038	C	T	42	GENIC	homozygous	113695226
5	25348210	25348211	G	A	45	GENIC	homozygous	113695228
5	25348576	25348577	A	G	51	GENIC	homozygous	113695230
5	25350039	25350040	A	G	54	GENIC	homozygous	113695232
5	25352982	25352983	C	T	59	GENIC	homozygous	113695234
5	25353419	25353420	G	T	59	GENIC	homozygous	113695236