chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95188461	95188462	C	T	46	GENIC	homozygous	52056468
9	95188739	95188740	T	C	40	GENIC	homozygous	52056471
9	95189670	95189671	A	G	61	GENIC	possibly homozygous	52056473
9	95189943	95189944	A	C	77	GENIC	homozygous	52056475
9	95190174	95190175	T	A	63	GENIC	homozygous	52281375
9	95190434	95190435	G	A	38	GENIC	possibly homozygous	52281376
9	95190557	95190558	C	CTT	19	GENIC	homozygous	52056477
9	95190768	95190769	G	C	43	GENIC	homozygous	52281377
9	95193762	95193763	T	TTC	15	GENIC	heterozygous	52056481
9	95193763	95193765	TC	--	15	GENIC	heterozygous	52056482
9	95194895	95194896	C	CAG	20	GENIC	homozygous	52056486
9	95194940	95194946	ACACAC	------	15	GENIC	possibly homozygous	52056488
9	95195170	95195171	A	T	44	GENIC	homozygous	52056492
9	95195422	95195423	A	T	61	GENIC	homozygous	52056494
9	95197147	95197149	CA	--	40	GENIC	heterozygous	52056500
9	95198496	95198498	AA	--	38	GENIC	heterozygous	52281378
9	95198518	95198519	A	AC	42	GENIC	heterozygous	52436734
9	95200072	95200073	A	AACAC	17	GENIC	heterozygous	52056504
9	95200072	95200073	A	AAC	17	GENIC	heterozygous	52281379
9	95200402	95200403	C	T	61	GENIC	homozygous	52281380
9	95200708	95200709	T	A	26	GENIC	homozygous	52056506
9	95201597	95201598	C	T	50	GENIC	possibly homozygous	52281381
9	95201760	95201761	T	TC	4	GENIC	homozygous	52056512
9	95202948	95202949	T	C	52	GENIC	homozygous	52056516
9	95203464	95203465	G	A	39	GENIC	homozygous	52281382
9	95205135	95205136	A	G	63	GENIC	possibly homozygous	52281383
9	95205240	95205241	C	CCATAT	37	GENIC	homozygous	52056518
9	95205552	95205558	ATTACC	------	34	GENIC	heterozygous	52056520
9	95205553	95205554	T	TCA	34	GENIC	homozygous	52056522
9	95205557	95205558	C	CAT	37	GENIC	homozygous	52056524
9	95207367	95207368	C	T	62	GENIC	homozygous	52281384