chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	30161084	30161085	A	G	51	GENIC	homozygous	115304028
12	30164486	30164487	A	C	35	GENIC	homozygous	115304030
12	30165458	30165459	G	T	43	GENIC	homozygous	115304033
12	30165889	30165890	G	A	48	GENIC	homozygous	115304035
12	30166404	30166405	C	T	52	GENIC	homozygous	115304037
12	30166449	30166450	C	T	47	GENIC	homozygous	115304039
12	30171217	30171218	T	C	44	GENIC	homozygous	115304047
12	30163764	30163765	G	A	52	GENIC	homozygous	134861444
12	30166307	30166308	T		54	GENIC	possibly homozygous	128980229
12	30169181	30169181		AA	12	GENIC	heterozygous	128980230
12	30169435	30169435		AAT	29	GENIC	homozygous	128980231
12	30169531	30169541	CAGCGAGTTC		48	GENIC	homozygous	128980232
12	30166464	30166465	C	A	44	GENIC	homozygous	115304041
12	30167445	30167446	A	G	33	GENIC	homozygous	115304043
12	30170287	30170288	A	G	52	GENIC	homozygous	115304045
12	30168240	30168241	C	A	40	GENIC	homozygous	118263945
12	30171243	30171244	G	A	43	GENIC	homozygous	115304049
12	30171317	30171320	CTC		45	GENIC	homozygous	128980233
12	30171627	30171628	G	A	45	GENIC	homozygous	115304051
12	30171980	30171981	T		15	GENIC	homozygous	128980234
12	30172688	30172689	T	G	40	GENIC	homozygous	115304053
12	30172829	30172830	A	C	42	GENIC	homozygous	115304055
12	30174633	30174634	C	T	23	GENIC	homozygous	115304057
12	30175005	30175006	G	A	43	GENIC	homozygous	115304059
12	30175099	30175100	C	T	47	GENIC	homozygous	115304061
12	30176130	30176131	G	A	36	GENIC	homozygous	115304063
12	30176322	30176323	T	G	36	GENIC	homozygous	115304065
12	30177099	30177100	T	C	37	GENIC	homozygous	115304067
12	30177139	30177140	C	T	32	GENIC	homozygous	118263949
12	30177201	30177202	T	C	48	GENIC	possibly homozygous	115304069
12	30177318	30177319	G	A	41	GENIC	possibly homozygous	115304071
12	30177452	30177453	G	C	44	GENIC	homozygous	115304073
12	30177454	30177455	T	A	44	GENIC	homozygous	115304075
12	30177583	30177584	T	C	50	GENIC	possibly homozygous	115304077