chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24160250	24160251	T	C	17	GENIC	homozygous	50131913
12	24161030	24161031	C	A	44	GENIC	homozygous	50439047
12	24161094	24161095	T	A	34	GENIC	homozygous	50131915
12	24161097	24161098	C	T	34	GENIC	homozygous	50131917
12	24161815	24161816	T	TCG	11	GENIC	homozygous	50439049
12	24161816	24161817	A	ATCTC	11	GENIC	heterozygous	50538426
12	24161988	24161989	T	C	42	GENIC	homozygous	50131923
12	24162402	24162403	T	A	54	GENIC	homozygous	50131927
12	24162708	24162709	T	A	56	GENIC	homozygous	50439051
12	24163590	24163591	A	G	57	GENIC	homozygous	50131929
12	24163771	24163772	C	T	42	GENIC	homozygous	50131931
12	24164446	24164447	T	C	66	GENIC	homozygous	50131933
12	24164471	24164472	C	T	64	GENIC	homozygous	50131935
12	24164597	24164598	G	A	40	GENIC	homozygous	50131937
12	24164618	24164619	T	C	53	GENIC	homozygous	50131939
12	24165085	24165086	A	AACAC	11	GENIC	heterozygous	50292652
12	24165085	24165086	A	AAC	11	GENIC	heterozygous	50538427
12	24165123	24165124	T	C	21	GENIC	homozygous	50538428
12	24165125	24165126	T	C	21	GENIC	homozygous	50538429
12	24165385	24165386	A	G	58	GENIC	homozygous	50131943
12	24165574	24165575	T	A	56	GENIC	homozygous	50131946
12	24165815	24165816	A	G	37	GENIC	homozygous	50131948
12	24166349	24166350	C	T	39	GENIC	homozygous	50131952
12	24166688	24166689	G	C	30	GENIC	homozygous	50131954
12	24167215	24167216	G	A	69	GENIC	homozygous	50131956
12	24167418	24167419	C	T	29	GENIC	homozygous	50439053
12	24167535	24167536	C	T	19	GENIC	homozygous	50131958
12	24167707	24167708	A	G	41	GENIC	homozygous	50131960
12	24167748	24167749	A	G	38	GENIC	homozygous	50131962
12	24168004	24168005	G	A	27	GENIC	homozygous	50131965
12	24168915	24168916	T	TTGTC	39	GENIC	homozygous	50131968
12	24168952	24168953	T	C	64	GENIC	homozygous	50131970
12	24169403	24169404	T	C	66	GENIC	homozygous	50131972
12	24170307	24170308	G	A	28	GENIC	homozygous	50131974
12	24170354	24170355	C	T	26	GENIC	homozygous	50131977
12	24170518	24170519	G	A	35	GENIC	homozygous	50131983