chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	16900295	16900296	A	G	57	GENIC	homozygous	139095253
12	16906400	16906400		T	1	GENIC	homozygous	144098329
12	16910006	16910007	G	C	5	GENIC	heterozygous	403318270
12	16909982	16909983	G	C	5	GENIC	heterozygous	154743542
12	16908684	16908684		TCTGTGTGTGTGCGTGGGTGTGGGTG	54	GENIC	homozygous	139043501
12	16908704	16908704		TG	40	GENIC	possibly homozygous	139043502
12	16909982	16909983	G		5	GENIC	heterozygous	403318266
12	16909990	16909991	G		5	GENIC	heterozygous	403318267
12	16909990	16909991	G	C	5	GENIC	heterozygous	403318268
12	16910006	16910007	G		5	GENIC	heterozygous	403318269
12	16909998	16909999	G		5	GENIC	heterozygous	403737670
12	16909998	16909999	G	C	5	GENIC	heterozygous	403737671
12	16910002	16910003	G		5	GENIC	heterozygous	403845820
12	16910002	16910003	G	C	5	GENIC	heterozygous	403845821
12	16910014	16910015	G		5	GENIC	heterozygous	404020571
12	16909975	16910079	ATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATACATAGATACATAGATACATAGATAGATACATAGATACATAGATACATAGATACATAGATAG		5	GENIC	heterozygous	145216854
12	16910014	16910015	G	C	5	GENIC	heterozygous	404020572