chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	95761358	95761359	C	T	11	GENIC	homozygous	61478279
1	95761691	95761692	A	T	18	GENIC	possibly homozygous	61478280
1	95761948	95761949	C	T	36	GENIC	homozygous	61952602
1	95762173	95762174	G	A	16	GENIC	homozygous	61952603
1	95762325	95762326	T	C	25	GENIC	possibly homozygous	61478283
1	95762519	95762520	C	T	18	GENIC	possibly homozygous	61952604
1	95763560	95763561	T	A	10	GENIC	possibly homozygous	61952605
1	95763562	95763563	A	C	11	GENIC	homozygous	61478284
1	95763740	95763741	C	T	12	GENIC	homozygous	61952606
1	95763746	95763747	T	TGGATA	10	GENIC	possibly homozygous	61952607
1	95764640	95764641	T	C	15	GENIC	homozygous	61478285
1	95765198	95765199	A	G	23	GENIC	possibly homozygous	61478287
1	95765887	95765888	A	G	23	GENIC	homozygous	61478288
1	95765938	95765939	A	G	26	GENIC	possibly homozygous	61478289
1	95767033	95767034	A	G	19	GENIC	possibly homozygous	61478291
1	95767756	95767757	C	T	16	GENIC	possibly homozygous	61952608
1	95768139	95768140	G	A	25	GENIC	possibly homozygous	61952609
1	95768523	95768524	T	C	16	GENIC	homozygous	61478295
1	95768538	95768539	A	ATG	5	GENIC	heterozygous	61478296
1	95769069	95769070	T	C	8	GENIC	heterozygous	61478297