chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41203868	41203869	G	T	33	GENIC	homozygous	115384703
12	41204070	41204071	T	C	29	GENIC	homozygous	115329620
12	41204188	41204189	G	A	27	GENIC	homozygous	115384705
12	41204228	41204229	G	A	28	GENIC	possibly homozygous	115384707
12	41204242	41204243	G	A	30	GENIC	homozygous	115329624
12	41204347	41204348	G	T	27	GENIC	homozygous	115384709
12	41204603	41204604	T	C	37	GENIC	homozygous	115384711
12	41204753	41204754	T	C	35	GENIC	homozygous	115329626
12	41204785	41204786	T	A	35	GENIC	homozygous	115329628
12	41204978	41204979	G	A	29	GENIC	homozygous	115329630
12	41205974	41205975	T	C	27	GENIC	homozygous	115384715
12	41206413	41206414	G	C	42	GENIC	homozygous	115329634
12	41207136	41207137	T	C	29	GENIC	homozygous	115384717
12	41207177	41207178	A	G	22	GENIC	homozygous	115384719
12	41207508	41207509	G	A	23	GENIC	homozygous	115384723
12	41207558	41207559	T	C	30	GENIC	homozygous	115384725
12	41207590	41207591	A	G	34	GENIC	homozygous	115384727
12	41207676	41207677	A	G	18	GENIC	homozygous	115384729
12	41207702	41207703	A	T	20	GENIC	homozygous	115384731
12	41207885	41207886	T	G	24	GENIC	homozygous	115384737
12	41207899	41207900	T	C	22	GENIC	homozygous	115384739
12	41208371	41208372	A	G	19	GENIC	homozygous	115477909
12	41208380	41208381	T	C	18	GENIC	homozygous	115477911
12	41208529	41208530	T	A	28	GENIC	homozygous	115384745