chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2134525	2134526	A	C	14	GENIC	homozygous	115436611
12	2138452	2138453	C	T	24	GENIC	homozygous	115233687
12	2139024	2139025	A	G	22	GENIC	homozygous	115233693
12	2138576	2138577	T	A	20	GENIC	homozygous	115233689
12	2138577	2138578	T	A	20	GENIC	homozygous	115233691
12	2140671	2140672	T	A	18	GENIC	homozygous	115233695
12	2140814	2140815	T	C	15	GENIC	homozygous	115233697
12	2141214	2141215	A	G	16	GENIC	homozygous	115233699
12	2141539	2141540	A	T	22	GENIC	homozygous	115233701
12	2141547	2141548	G	C	24	GENIC	homozygous	115233703
12	2141555	2141556	G	C	21	GENIC	homozygous	115233705
12	2142897	2142898	T	C	19	GENIC	homozygous	115233707
12	2143245	2143246	C	T	19	GENIC	homozygous	115233709
12	2143561	2143562	C	T	18	GENIC	homozygous	115436612
12	2143758	2143759	G	A	31	GENIC	homozygous	115233711
12	2146877	2146878	T	C	24	GENIC	homozygous	115233713
12	2146949	2146950	T	C	28	GENIC	homozygous	115233715
12	2146994	2146995	C	G	31	GENIC	homozygous	115233717
12	2148341	2148342	C	T	18	GENIC	homozygous	115233719
12	2148813	2148814	G	C	19	GENIC	homozygous	115233721
12	2150734	2150735	T	A	27	GENIC	homozygous	115233723
12	2151151	2151152	C	T	22	GENIC	homozygous	115233725
12	2152114	2152115	T	C	15	GENIC	homozygous	115233727
12	2154299	2154300	C	T	25	GENIC	homozygous	115233731
12	2154357	2154358	T	G	27	GENIC	homozygous	115233733
12	2154595	2154596	G	T	14	GENIC	homozygous	115233735
12	2154754	2154755	T	C	21	GENIC	homozygous	115233737
12	2155125	2155126	A	G	9	GENIC	homozygous	115233739
12	2156303	2156304	T	C	20	GENIC	homozygous	115233741