chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	30161084	30161085	A	G	19	GENIC	homozygous	115304028
12	30164486	30164487	A	C	14	GENIC	homozygous	115304030
12	30165458	30165459	G	T	19	GENIC	homozygous	115304033
12	30165889	30165890	G	A	16	GENIC	homozygous	115304035
12	30166404	30166405	C	T	18	GENIC	homozygous	115304037
12	30166449	30166450	C	T	19	GENIC	homozygous	115304039
12	30166464	30166465	C	A	20	GENIC	homozygous	115304041
12	30167445	30167446	A	G	14	GENIC	homozygous	115304043
12	30169531	30169541	CAGCGAGTTC		20	GENIC	homozygous	128980232
12	30166307	30166308	T		10	GENIC	homozygous	128980229
12	30169181	30169181		AA	4	GENIC	homozygous	128980230
12	30169435	30169435		AAT	15	GENIC	homozygous	128980231
12	30168240	30168241	C	A	19	GENIC	possibly homozygous	118263945
12	30170287	30170288	A	G	28	GENIC	homozygous	115304045
12	30171217	30171218	T	C	22	GENIC	homozygous	115304047
12	30171243	30171244	G	A	25	GENIC	homozygous	115304049
12	30171317	30171320	CTC		21	GENIC	homozygous	128980233
12	30171627	30171628	G	A	19	GENIC	homozygous	115304051
12	30171980	30171981	T		22	GENIC	homozygous	128980234
12	30172688	30172689	T	G	18	GENIC	homozygous	115304053
12	30172829	30172830	A	C	19	GENIC	homozygous	115304055
12	30174633	30174634	C	T	16	GENIC	homozygous	115304057
12	30175005	30175006	G	A	19	GENIC	homozygous	115304059
12	30175099	30175100	C	T	13	GENIC	homozygous	115304061
12	30176130	30176131	G	A	17	GENIC	homozygous	115304063
12	30176322	30176323	T	G	19	GENIC	homozygous	115304065
12	30177318	30177319	G	A	30	GENIC	homozygous	115304071
12	30177099	30177100	T	C	28	GENIC	homozygous	115304067
12	30177139	30177140	C	T	27	GENIC	homozygous	118263949
12	30177201	30177202	T	C	27	GENIC	homozygous	115304069
12	30177452	30177453	G	C	21	GENIC	homozygous	115304073
12	30177454	30177455	T	A	21	GENIC	homozygous	115304075
12	30177583	30177584	T	C	22	GENIC	homozygous	115304077