chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41255881	41255882	T	G	47	GENIC	homozygous	118270774
12	41255902	41255903	C	T	54	GENIC	possibly homozygous	118270775
12	41256357	41256358	G	A	41	GENIC	homozygous	115486374
12	41256578	41256579	C	T	52	GENIC	homozygous	118270776
12	41256936	41256937	A	G	68	GENIC	homozygous	118270777
12	41257272	41257273	G	A	85	GENIC	heterozygous	118270778
12	41258120	41258121	G	A	57	GENIC	homozygous	118270779
12	41260475	41260476	A	G	37	GENIC	possibly homozygous	115477949
12	41261674	41261675	G	A	45	GENIC	homozygous	115329744
12	41258274	41258275	G	A	63	GENIC	homozygous	115329740
12	41260044	41260045	A	G	56	GENIC	homozygous	115329742
12	41262170	41262171	G	C	48	GENIC	heterozygous	118305263
12	41262370	41262371	A	G	37	GENIC	homozygous	115329746
12	41262599	41262600	G	A	52	GENIC	homozygous	115329748
12	41262851	41262852	C	G	62	GENIC	possibly homozygous	118270780
12	41263559	41263560	C	T	35	GENIC	homozygous	118270781
12	41263750	41263751	A	G	50	GENIC	homozygous	118270782
12	41263810	41263811	A	G	35	GENIC	homozygous	118270783
12	41263850	41263851	A	C	58	GENIC	homozygous	118270784
12	41263918	41263919	C	G	80	GENIC	possibly homozygous	115704368
12	41264102	41264103	C	T	55	GENIC	possibly homozygous	115329750
12	41264327	41264328	C	T	54	GENIC	homozygous	115329752