chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	1721786	1721787	G	A	15	GENIC	homozygous	139061479
12	1721786	1721787	G		15	GENIC	heterozygous	403844900
12	1721791	1721792	C	T	15	GENIC	homozygous	139061480
12	1721792	1721793	A	G	15	GENIC	homozygous	139061481
12	1722108	1722109	T	C	37	GENIC	homozygous	139061482
12	1722635	1722636	A	G	53	GENIC	homozygous	139061483
12	1722687	1722688	G	C	49	GENIC	homozygous	139061484
12	1722748	1722749	C	A	46	GENIC	homozygous	139061485
12	1722912	1722913	C	T	48	GENIC	homozygous	139061486
12	1723273	1723274	C	T	30	GENIC	homozygous	139061487
12	1723410	1723411	T	A	29	GENIC	homozygous	139061488
12	1723603	1723604	T	G	48	GENIC	possibly homozygous	139061489
12	1723912	1723913	T	C	60	GENIC	homozygous	139061490
12	1725303	1725304	T	C	47	GENIC	homozygous	139061491
12	1725867	1725868	C	T	39	GENIC	homozygous	139061492
12	1727332	1727333	G	T	58	GENIC	homozygous	139061493
12	1723337	1723338	A	C	15	GENIC	homozygous	154753818
12	1722834	1722834		T	49	GENIC	homozygous	139035731