chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89007612	89007613	C	T	57	GENIC	homozygous	116902154
10	89010491	89010492	A	T	50	GENIC	homozygous	116674956
10	89012417	89012418	C	T	71	GENIC	homozygous	116674964
10	89013868	89013869	C	T	61	GENIC	homozygous	116674966
10	89015542	89015543	A	G	62	GENIC	homozygous	116674970
10	89015704	89015705	A	T	48	GENIC	heterozygous	117144492
10	89015764	89015765	C	T	46	GENIC	homozygous	116674972
10	89016465	89016466	G	C	51	GENIC	homozygous	116674974
10	89017372	89017373	C	T	48	GENIC	homozygous	116902156
10	89017527	89017528	G	A	54	GENIC	homozygous	116674976
10	89017988	89017989	G	A	38	GENIC	homozygous	116902158
10	89020574	89020575	C	T	80	GENIC	heterozygous	118007471
10	89020919	89020920	T	C	26	GENIC	heterozygous	118048790
10	89023158	89023159	T	A	41	GENIC	homozygous	116819456
10	89023532	89023533	T	G	69	GENIC	homozygous	116674978
10	89025114	89025115	G	A	44	GENIC	homozygous	116674980
10	89025328	89025329	T	C	48	GENIC	homozygous	116819460
10	89025848	89025849	A	T	21	GENIC	homozygous	118007472
10	89025896	89025897	G	A	33	GENIC	heterozygous	116819464
10	89027198	89027199	C	T	40	GENIC	possibly homozygous	117180003
10	89021563	89021564	A	G	24	GENIC	heterozygous	117197713
10	89025846	89025847	A	G	22	GENIC	possibly homozygous	117227875
10	89029885	89029886	C	A	71	GENIC	homozygous	116674982