chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	63003134	63003135	G	A	29	GENIC	homozygous	116838225
8	63003388	63003389	T	C	21	GENIC	homozygous	117143433
8	63003552	63003553	C	T	19	GENIC	homozygous	117143435
8	63003949	63003950	A	C	26	GENIC	homozygous	117143437
8	63003960	63003961	C	T	30	GENIC	homozygous	117143439
8	63004431	63004432	G	A	43	GENIC	homozygous	117143441
8	63004622	63004623	G	A	31	GENIC	homozygous	117143443
8	63006629	63006630	C	G	26	GENIC	homozygous	117143445
8	63006750	63006751	T	G	21	GENIC	homozygous	116838239
8	63007014	63007015	G	A	28	GENIC	possibly homozygous	117143447
8	63007337	63007338	T	C	24	GENIC	homozygous	116838241
8	63007596	63007597	G	A	23	GENIC	homozygous	117143449
8	63007991	63007992	A	G	32	GENIC	homozygous	117143451
8	63008033	63008034	A	G	20	GENIC	homozygous	116838243
8	63008754	63008755	G	A	32	GENIC	homozygous	117143453
8	63009492	63009493	A	G	24	GENIC	homozygous	117143455
8	63010565	63010566	T	C	48	GENIC	homozygous	116838263
8	63010668	63010669	C	T	33	GENIC	homozygous	117143457
8	63015530	63015531	C	T	31	GENIC	homozygous	116838269
8	63016382	63016383	G	T	15	GENIC	homozygous	117143459
8	63020917	63020918	T	C	32	GENIC	homozygous	116838275
8	63022459	63022460	G	C	19	GENIC	homozygous	116838277
8	63024335	63024336	T	A	19	GENIC	homozygous	116838283
8	63026246	63026247	T	A	28	GENIC	homozygous	117158499
8	63026247	63026248	A	G	27	GENIC	homozygous	117944192
8	63029091	63029092	T	C	19	GENIC	homozygous	116838289
8	63029484	63029485	A	G	20	GENIC	homozygous	116838291
8	63030373	63030374	T	C	8	GENIC	homozygous	117143461
8	63031705	63031706	G	A	25	GENIC	homozygous	117143463
8	63031749	63031750	C	T	21	GENIC	homozygous	117143465
8	63032099	63032100	C	G	33	GENIC	homozygous	117143467
8	63032387	63032388	C	G	28	GENIC	homozygous	117143469
8	63032945	63032946	C	G	10	GENIC	homozygous	117143471
8	63033151	63033152	G	A	13	GENIC	homozygous	117143473
8	63034111	63034112	A	G	45	GENIC	homozygous	117143475