chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42480898	42480899	G	A	28	GENIC	homozygous	115331360
12	42481446	42481447	T	C	32	GENIC	homozygous	115331362
12	42482185	42482186	C	A	6	GENIC	homozygous	115331364
12	42487728	42487729	T	C	26	GENIC	homozygous	115331366
12	42489556	42489557	C	T	16	GENIC	homozygous	115331368
12	42490416	42490417	A	G	19	GENIC	homozygous	115331370
12	42492457	42492458	T	C	16	GENIC	possibly homozygous	115331372
12	42493812	42493813	T	A	21	GENIC	homozygous	115331374
12	42494137	42494138	C	G	41	GENIC	homozygous	115331376
12	42494398	42494399	C	T	35	GENIC	homozygous	115331378
12	42494466	42494467	A	G	42	GENIC	homozygous	115331380
12	42494491	42494492	A	G	39	GENIC	homozygous	115331382