chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	1721789	1721789		CA	31	GENIC	homozygous	144912116
12	1721819	1721819		CG	32	GENIC	homozygous	144912117
12	1722108	1722109	T	C	57	GENIC	homozygous	139061482
12	1722635	1722636	A	G	62	GENIC	homozygous	139061483
12	1722687	1722688	G	C	58	GENIC	homozygous	139061484
12	1722769	1722770	A	G	51	GENIC	homozygous	144915428
12	1722912	1722913	C	T	42	GENIC	homozygous	139061486
12	1723254	1723254		TT	39	GENIC	homozygous	144912118
12	1723273	1723274	C	T	40	GENIC	homozygous	139061487
12	1723337	1723338	A	C	19	GENIC	homozygous	154753818
12	1723410	1723411	T	A	19	GENIC	homozygous	139061488
12	1723603	1723604	T	G	49	GENIC	homozygous	139061489
12	1723774	1723775	G	A	72	GENIC	homozygous	144915429
12	1723955	1723956	G	A	56	GENIC	homozygous	144915430
12	1725303	1725304	T	C	41	GENIC	possibly homozygous	139061491
12	1725867	1725868	C	T	53	GENIC	homozygous	139061492