chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479627	42479627		TTG	30	GENIC	homozygous	131118910
12	42479664	42479665	T		27	GENIC	homozygous	128991452
12	42482004	42482006	AC		22	GENIC	possibly homozygous	131118911
12	42482185	42482186	C	A	11	GENIC	homozygous	115331364
12	42482242	42482248	GGGGTG		8	GENIC	homozygous	132167282
12	42487728	42487729	T	C	23	GENIC	homozygous	115331366
12	42489556	42489557	C	T	42	GENIC	homozygous	115331368
12	42489562	42489563	C	T	45	GENIC	homozygous	115428295
12	42483540	42483541	G	A	46	GENIC	homozygous	115428291
12	42483935	42483936	G	C	41	GENIC	homozygous	115428293
12	42489806	42489807	G	A	41	GENIC	homozygous	115428297
12	42490416	42490417	A	G	22	GENIC	homozygous	115331370
12	42490647	42490648	G	A	3	GENIC	homozygous	115428301
12	42490889	42490890	G	A	36	GENIC	homozygous	115428303
12	42491162	42491163	T	C	30	GENIC	homozygous	115428305
12	42491373	42491374	A	G	41	GENIC	homozygous	115428307
12	42491814	42491815	G	A	45	GENIC	homozygous	115428309
12	42492971	42492972	G	C	39	GENIC	homozygous	115428311
12	42493115	42493115		A	33	GENIC	homozygous	131118913
12	42493684	42493685	A	G	41	GENIC	homozygous	115428313
12	42494006	42494007	C	T	38	GENIC	homozygous	115428315
12	42494398	42494399	C	T	32	GENIC	homozygous	115331378
12	42494466	42494467	A	G	38	GENIC	homozygous	115331380