chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16663258	16663259	C	T	12	GENIC	homozygous	139094901
12	16663280	16663280		CT	21	GENIC	possibly homozygous	139043378
12	16663758	16663759	C	T	41	GENIC	homozygous	139094902
12	16663770	16663771	G	A	41	GENIC	homozygous	139094903
12	16663860	16663861	T	C	43	GENIC	homozygous	139094904
12	16664184	16664185	A	G	55	GENIC	homozygous	139094905
12	16664225	16664226	G	A	56	GENIC	homozygous	139094906
12	16665044	16665045	T	C	27	GENIC	homozygous	139094907
12	16665102	16665102		T	36	GENIC	homozygous	139043379
12	16665433	16665433		AAAAA	35	GENIC	homozygous	139043380
12	16665728	16665734	TAGGTT		40	GENIC	homozygous	139043381
12	16666141	16666142	C		21	GENIC	homozygous	139043382
12	16666620	16666621	T	C	18	GENIC	homozygous	139094908
12	16666814	16666815	C	T	34	GENIC	homozygous	139094909
12	16667636	16667637	A	T	55	GENIC	possibly homozygous	139094910
12	16668238	16668239	T	C	38	GENIC	homozygous	139094911
12	16668868	16668869	C	T	36	GENIC	homozygous	139094912
12	16669012	16669012		T	37	GENIC	homozygous	139043383
12	16669511	16669512	G	A	27	GENIC	homozygous	139094913
12	16669943	16669944	G	T	37	GENIC	possibly homozygous	139094914