chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	12878565	12878566	A	T	32	GENIC	homozygous	115259372
12	12881219	12881220	G	A	27	GENIC	heterozygous	118245253
12	12881230	12881231	C	T	26	GENIC	heterozygous	118245254
12	12884576	12884577	C	T	44	GENIC	homozygous	115259374
12	12885777	12885778	A	G	44	GENIC	heterozygous	118292283
12	12885791	12885792	A	G	66	GENIC	heterozygous	118245255
12	12885881	12885882	T	C	46	GENIC	heterozygous	118292284
12	12893252	12893253	C	T	39	GENIC	homozygous	115259376
12	12897665	12897666	A	G	32	GENIC	homozygous	115259378
12	12899459	12899460	C	T	52	GENIC	possibly homozygous	115259380
12	12899874	12899875	G	A	47	GENIC	homozygous	115259382
12	12900142	12900143	C	A	55	GENIC	possibly homozygous	115259384
12	12900231	12900232	G	A	20	GENIC	homozygous	115259386
12	12900241	12900242	C	T	15	GENIC	homozygous	115259388
12	12900791	12900792	T	G	38	GENIC	homozygous	115259390
12	12905762	12905763	A	G	39	GENIC	homozygous	115259392
12	12905800	12905801	C	T	41	GENIC	homozygous	115259394