chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6465094	6465095	C	T	70	GENIC	homozygous	130037396
20	6465146	6465147	A	T	68	GENIC	homozygous	130037397
20	6495758	6495759	T		20	GENIC	homozygous	129980604
20	6501703	6501704	A	G	60	GENIC	homozygous	130037400
20	6511877	6511878	G	C	19	GENIC	heterozygous	147763788
20	6521352	6521353	A	C	62	GENIC	homozygous	130037403
20	6545545	6545546	A	G	52	GENIC	homozygous	145088093
20	6521257	6521258	A		34	GENIC	heterozygous	403462708
20	6521257	6521258	A	C	34	GENIC	heterozygous	403462709
20	6505194	6505195	G	T	60	GENIC	homozygous	145088090
20	6508295	6508296	C	A	68	GENIC	possibly homozygous	145088091
20	6511337	6511338	G	A	49	GENIC	homozygous	145088092
20	6528031	6528033	TG		33	GENIC	homozygous	145084203
20	6562812	6562813	A	T	47	GENIC	heterozygous	155134908
20	6565755	6565760	TCTAC		25	GENIC	homozygous	145084204
20	6566391	6566392	T	A	34	GENIC	homozygous	130037422
20	6566675	6566676	A	G	42	GENIC	homozygous	130037424
20	6566856	6566857	C	G	63	GENIC	homozygous	145088094
20	6570554	6570555	A	G	54	GENIC	homozygous	130037427
20	6571440	6571441	C	T	57	GENIC	homozygous	130037428
20	6562812	6562813	A		47	GENIC	heterozygous	403680814
20	6573153	6573154	A	G	66	GENIC	homozygous	130037429
20	6574459	6574460	G		38	GENIC	homozygous	129980609
20	6574598	6574599	A		48	GENIC	homozygous	129980610