chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2134525	2134526	A	C	11	GENIC	homozygous	115436611
12	2138417	2138418	G	A	33	GENIC	homozygous	115357237
12	2139024	2139025	A	G	25	GENIC	homozygous	115233693
12	2140624	2140625	G	A	26	GENIC	homozygous	115357238
12	2141214	2141215	A	G	30	GENIC	homozygous	115233699
12	2141539	2141540	A	T	14	GENIC	homozygous	115233701
12	2141547	2141548	G	C	13	GENIC	homozygous	115233703
12	2141555	2141556	G	C	14	GENIC	homozygous	115233705
12	2141889	2141890	G	A	24	GENIC	homozygous	115357239
12	2142477	2142478	C	A	21	GENIC	homozygous	115357240
12	2143569	2143570	T	C	16	GENIC	homozygous	115357241
12	2148813	2148814	G	C	26	GENIC	homozygous	115233721
12	2150734	2150735	T	A	18	GENIC	homozygous	115233723
12	2151632	2151633	C	T	27	GENIC	possibly homozygous	115461233
12	2149465	2149466	C	T	26	GENIC	homozygous	115461229
12	2150387	2150388	C	A	28	GENIC	homozygous	115461231
12	2149554	2149555	G	C	25	GENIC	homozygous	115678295
12	2151958	2151959	C	T	19	GENIC	homozygous	115461236
12	2152096	2152097	G	A	17	GENIC	homozygous	115461238
12	2152114	2152115	T	C	20	GENIC	homozygous	115233727
12	2152729	2152730	C	T	16	GENIC	possibly homozygous	115461241
12	2154357	2154358	T	G	18	GENIC	homozygous	115233733
12	2154595	2154596	G	T	20	GENIC	possibly homozygous	115233735
12	2154754	2154755	T	C	15	GENIC	homozygous	115233737
12	2157173	2157174	C	G	27	GENIC	possibly homozygous	115461247