chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	6880432	6880433	T	A	59	GENIC	homozygous	141801302
6	6880459	6880460	A	G	64	GENIC	homozygous	141801303
6	6880980	6880980		CA	54	GENIC	homozygous	141774121
6	6881245	6881246	T	C	71	GENIC	homozygous	141801304
6	6881758	6881759	A	T	55	GENIC	homozygous	141801305
6	6881813	6881814	A	G	61	GENIC	homozygous	141801306
6	6882528	6882529	G	C	46	GENIC	homozygous	141801307
6	6883768	6883769	G	A	59	GENIC	homozygous	141801308
6	6884590	6884591	A	G	50	GENIC	homozygous	141801309
6	6884886	6884887	A	G	52	GENIC	homozygous	141801310
6	6888491	6888492	C	T	43	GENIC	homozygous	141801311
6	6889896	6889897	A	G	44	GENIC	homozygous	141801312
6	6890574	6890575	A	G	15	GENIC	heterozygous	141801313
6	6890576	6890577	A	G	19	GENIC	homozygous	141801314
6	6890578	6890579	A	G	19	GENIC	homozygous	141801315
6	6890580	6890581	A	G	18	GENIC	homozygous	141801316
6	6891384	6891385	G	A	49	GENIC	possibly homozygous	141801317
6	6892200	6892201	C	T	46	GENIC	homozygous	141801318
6	6894346	6894350	TTTG		34	GENIC	possibly homozygous	141774122
6	6895660	6895661	G	A	44	GENIC	homozygous	141801319
6	6895709	6895710	C	T	49	GENIC	homozygous	141801320
6	6888455	6888456	G	A	49	GENIC	heterozygous	145141840
6	6881758	6881759	A		55	GENIC	heterozygous	403165838
6	6894331	6894332	G		44	GENIC	heterozygous	403165839
6	6888460	6888461	T	C	46	GENIC	heterozygous	145141841
6	6888464	6888465	A	G	46	GENIC	heterozygous	145141842
6	6894331	6894332	G	T	44	GENIC	homozygous	154340988
6	6895803	6895804	T	C	49	GENIC	homozygous	141801321