chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95188461	95188462	C	T	11	GENIC	possibly homozygous	52056468
9	95188487	95188488	T	-	2	GENIC	homozygous	52281374
9	95188739	95188740	T	C	19	GENIC	heterozygous	52056471
9	95189670	95189671	A	G	25	GENIC	possibly homozygous	52056473
9	95189943	95189944	A	C	23	GENIC	homozygous	52056475
9	95190174	95190175	T	A	29	GENIC	possibly homozygous	52281375
9	95190434	95190435	G	A	19	GENIC	homozygous	52281376
9	95190768	95190769	G	C	19	GENIC	possibly homozygous	52281377
9	95194895	95194896	C	CAG	9	GENIC	homozygous	52056486
9	95195170	95195171	A	T	21	GENIC	homozygous	52056492
9	95195422	95195423	A	T	20	GENIC	homozygous	52056494
9	95200402	95200403	C	T	26	GENIC	homozygous	52281380
9	95200708	95200709	T	A	11	GENIC	heterozygous	52056506
9	95201597	95201598	C	T	33	GENIC	possibly homozygous	52281381
9	95202948	95202949	T	C	7	GENIC	heterozygous	52056516
9	95203464	95203465	G	A	18	GENIC	homozygous	52281382
9	95205135	95205136	A	G	21	GENIC	heterozygous	52281383
9	95205240	95205241	C	CCATAT	2	GENIC	homozygous	52056518
9	95205553	95205554	T	TCA	1	GENIC	homozygous	52056522
9	95205557	95205558	C	CAT	4	GENIC	heterozygous	52056524
9	95207367	95207368	C	T	27	GENIC	possibly homozygous	52281384