chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95188461	95188462	C	T	41	GENIC	homozygous	52056468
9	95188664	95188665	G	C	49	GENIC	homozygous	52056469
9	95188739	95188740	T	C	53	GENIC	homozygous	52056471
9	95189670	95189671	A	G	55	GENIC	homozygous	52056473
9	95189943	95189944	A	C	61	GENIC	homozygous	52056475
9	95190557	95190558	C	CTT	20	GENIC	homozygous	52056477
9	95190936	95190937	G	A	41	GENIC	homozygous	52056479
9	95193762	95193763	T	TTC	6	GENIC	heterozygous	52056481
9	95193763	95193765	TC	--	6	GENIC	heterozygous	52056482
9	95194782	95194783	G	A	24	GENIC	heterozygous	52056484
9	95194895	95194896	C	CAG	20	GENIC	homozygous	52056486
9	95194940	95194946	ACACAC	------	16	GENIC	homozygous	52056488
9	95195095	95195096	C	T	40	GENIC	homozygous	52056490
9	95195170	95195171	A	T	29	GENIC	possibly homozygous	52056492
9	95195422	95195423	A	T	30	GENIC	homozygous	52056494
9	95196381	95196382	G	GT	40	GENIC	homozygous	52056496
9	95196697	95196698	G	A	49	GENIC	homozygous	52056498
9	95197147	95197149	CA	--	29	GENIC	heterozygous	52056500
9	95198111	95198112	C	T	57	GENIC	homozygous	52056502
9	95200072	95200073	A	AACAC	9	GENIC	possibly homozygous	52056504
9	95200708	95200709	T	A	28	GENIC	homozygous	52056506
9	95200914	95200915	G	GGA	13	GENIC	homozygous	52056508
9	95201736	95201737	T	G	8	GENIC	homozygous	52056510
9	95201760	95201761	T	TC	1	GENIC	homozygous	52056512
9	95201991	95201992	A	G	41	GENIC	homozygous	52056514
9	95202948	95202949	T	C	41	GENIC	homozygous	52056516
9	95205240	95205241	C	CCATAT	9	GENIC	homozygous	52056518
9	95205552	95205558	ATTACC	------	17	GENIC	heterozygous	52056520
9	95205553	95205554	T	TCA	17	GENIC	homozygous	52056522
9	95205557	95205558	C	CAT	13	GENIC	homozygous	52056524
9	95205584	95205585	C	CG	15	GENIC	possibly homozygous	52056526
9	95206020	95206021	G	-	39	GENIC	homozygous	52056528
9	95206066	95206067	C	T	58	GENIC	homozygous	52056530