chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	943154	943155	T	G	34	GENIC	possibly homozygous	115230863
12	945889	945890	G	C	56	GENIC	homozygous	115230865
12	946158	946159	G	C	37	GENIC	homozygous	115230867
12	946208	946209	C	G	52	GENIC	possibly homozygous	115230869
12	946304	946305	C	T	62	GENIC	homozygous	115230872
12	946707	946708	G	C	33	GENIC	homozygous	115577842
12	950788	950789	A	C	23	GENIC	homozygous	115230874
12	957597	957598	T	C	41	GENIC	homozygous	115230876
12	957827	957828	A	C	20	GENIC	homozygous	115230878
12	958581	958582	T	C	45	GENIC	homozygous	115230880
12	962630	962631	C	A	43	GENIC	homozygous	115230882
12	964186	964187	G	A	17	GENIC	homozygous	115230885
12	964829	964830	G	T	31	GENIC	homozygous	115230887
12	971499	971500	G	T	41	GENIC	homozygous	115230889
12	971982	971983	G	A	27	GENIC	homozygous	115230891
12	955628	955629	A	G	50	GENIC	homozygous	118234586
12	955777	955778	G	A	37	GENIC	heterozygous	118234587
12	955784	955785	C	T	38	GENIC	heterozygous	118234588
12	955800	955801	G	A	35	GENIC	heterozygous	118234589
12	956012	956013	T	G	51	GENIC	possibly homozygous	118234590
12	959845	959846	G	A	40	GENIC	heterozygous	118234591
12	969189	969190	T	A	14	GENIC	homozygous	115480950
12	971713	971714	G	C	64	GENIC	possibly homozygous	115436552
12	972181	972182	C	A	14	GENIC	homozygous	118234592
12	972504	972505	G	A	49	GENIC	homozygous	115436555
12	985224	985225	G	A	27	GENIC	possibly homozygous	115230894
12	986051	986052	T	C	54	GENIC	possibly homozygous	115230896