chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	64115017	64115018	C	A	17	GENIC	homozygous	118023047
8	64118842	64118843	A	G	18	GENIC	homozygous	118023049
8	64119158	64119159	T	C	21	GENIC	homozygous	116840291
8	64122095	64122096	T	C	19	GENIC	homozygous	118023051
8	64124883	64124884	A	G	13	GENIC	homozygous	118023053
8	64125771	64125772	T	C	19	GENIC	homozygous	116840297
8	64127670	64127670		CAGACTTAAAGAGTCC	22	GENIC	homozygous	130363962
8	64127789	64127790	T	C	9	GENIC	homozygous	116840299
8	64127812	64127813	A	C	9	GENIC	homozygous	122982615
8	64128417	64128417		A	17	GENIC	homozygous	134292970
8	64129272	64129273	T	G	14	GENIC	homozygous	117159995
8	64129273	64129274	A	T	14	GENIC	homozygous	117184850
8	64132530	64132531	A	G	20	GENIC	homozygous	116840305
8	64133776	64133777	G	A	15	GENIC	homozygous	118023055
8	64134758	64134759	C	T	22	GENIC	homozygous	118023057
8	64136695	64136696	G	A	24	GENIC	possibly homozygous	118023059
8	64136809	64136810	G	A	27	GENIC	homozygous	118023061
8	64136987	64136988	T	C	18	GENIC	homozygous	116840315
8	64138576	64138576		AACCCTT	20	GENIC	homozygous	130363964
8	64139126	64139127	A	G	22	GENIC	homozygous	116840319
8	64141871	64141872	T	A	12	GENIC	homozygous	116840325
8	64146042	64146043	G	T	23	GENIC	homozygous	116840327
8	64146442	64146442		T	20	GENIC	homozygous	130363966
8	64146814	64146815	C	A	19	GENIC	homozygous	116840329
8	64146861	64146862	A	T	19	GENIC	homozygous	116840331
8	64146970	64146970		T	21	GENIC	homozygous	130363968
8	64147149	64147150	A	T	16	GENIC	homozygous	116840333
8	64149704	64149705	T	G	19	GENIC	homozygous	116840337
8	64154222	64154223	A	C	11	GENIC	homozygous	116840339