chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	30161084	30161085	A	G	34	GENIC	homozygous	115304028
12	30163214	30163215	C	A	35	GENIC	heterozygous	118341777
12	30164486	30164487	A	C	33	GENIC	homozygous	115304030
12	30165458	30165459	G	T	39	GENIC	homozygous	115304033
12	30166404	30166405	C	T	29	GENIC	homozygous	115304037
12	30166449	30166450	C	T	47	GENIC	homozygous	115304039
12	30166464	30166465	C	A	51	GENIC	homozygous	115304041
12	30166939	30166940	T	A	28	GENIC	homozygous	115562029
12	30166941	30166942	A	C	27	GENIC	homozygous	115562031
12	30167445	30167446	A	G	29	GENIC	homozygous	115304043
12	30168373	30168374	G	A	25	GENIC	possibly homozygous	115562033
12	30169455	30169456	C	T	26	GENIC	homozygous	118263946
12	30170287	30170288	A	G	35	GENIC	homozygous	115304045
12	30171217	30171218	T	C	38	GENIC	homozygous	115304047
12	30172688	30172689	T	G	27	GENIC	homozygous	115304053
12	30172829	30172830	A	C	29	GENIC	homozygous	115304055
12	30173055	30173056	C	T	22	GENIC	heterozygous	118263947
12	30173065	30173066	C	T	25	GENIC	heterozygous	118263948
12	30173075	30173076	C	T	29	GENIC	heterozygous	118303216
12	30176130	30176131	G	A	28	GENIC	homozygous	115304063
12	30176322	30176323	T	G	31	GENIC	homozygous	115304065
12	30177010	30177011	T	C	40	GENIC	homozygous	115562035
12	30177099	30177100	T	C	34	GENIC	homozygous	115304067
12	30177201	30177202	T	C	38	GENIC	homozygous	115304069
12	30177264	30177265	A	G	37	GENIC	homozygous	115562037
12	30177318	30177319	G	A	38	GENIC	homozygous	115304071
12	30177583	30177584	T	C	32	GENIC	homozygous	115304077