chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	83996498	83996499	G	A	28	GENIC	homozygous	403292527
10	83996498	83996499	G		28	GENIC	heterozygous	403292528
10	83996502	83996502		T	15	GENIC	homozygous	138695373
10	83997237	83997239	CT		55	GENIC	homozygous	138695374
10	83999236	83999237	T	C	47	GENIC	homozygous	138836626
10	83997398	83997399	T	G	62	GENIC	homozygous	138836623
10	83998364	83998365	C	T	49	GENIC	homozygous	138836624
10	83999222	83999223	G	A	43	GENIC	homozygous	138836625
10	83999893	83999894	C	G	25	GENIC	homozygous	138836627
10	84000489	84000490	A	G	40	GENIC	homozygous	138836628
10	84000531	84000532	A		24	GENIC	possibly homozygous	138695375
10	84000572	84000573	C		32	GENIC	homozygous	138695376
10	84000574	84000576	AC		32	GENIC	homozygous	138695377
10	84002196	84002197	C		43	GENIC	homozygous	138695378
10	84002859	84002860	C	T	57	GENIC	homozygous	138836629
10	84002987	84002988	T	C	56	GENIC	homozygous	138836630
10	84003908	84003909	G	A	31	GENIC	homozygous	138836631
10	84004039	84004040	A	G	46	GENIC	homozygous	138836632
10	84004783	84004783		TATC	49	GENIC	possibly homozygous	138695379
10	84006456	84006456		TCA	46	GENIC	homozygous	138695380
10	84004058	84004059	G	A	43	GENIC	homozygous	138836633
10	84005895	84005896	T	G	39	GENIC	homozygous	138836634
10	84007140	84007141	C	T	41	GENIC	homozygous	138836635
10	84007168	84007169	T	A	43	GENIC	homozygous	138836636