chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17472601	17472602	C	A	41	GENIC	homozygous	115273904
12	17474504	17474505	G	A	25	GENIC	homozygous	115273906
12	17474640	17474641	A	G	39	GENIC	homozygous	115273908
12	17475603	17475604	G	A	29	GENIC	homozygous	115483545
12	17477373	17477374	C	T	29	GENIC	homozygous	115273910
12	17477962	17477963	A	T	29	GENIC	homozygous	115273912
12	17478031	17478032	C	G	39	GENIC	homozygous	115273914
12	17479122	17479123	T	C	30	GENIC	homozygous	115273916
12	17479246	17479247	C	T	15	GENIC	homozygous	115273918
12	17479720	17479721	C	T	30	GENIC	homozygous	115273920
12	17479752	17479753	C	T	37	GENIC	homozygous	115273922
12	17480137	17480138	G	A	23	GENIC	homozygous	115483546
12	17480995	17480996	T	C	44	GENIC	homozygous	115273924
12	17481068	17481069	C	T	31	GENIC	homozygous	115483547
12	17481114	17481115	T	C	34	GENIC	homozygous	115273926
12	17481346	17481347	G	A	37	GENIC	homozygous	115273928
12	17481569	17481570	C	T	29	GENIC	homozygous	115273930
12	17481703	17481704	T	A	32	GENIC	homozygous	115273932
12	17481763	17481764	C	T	24	GENIC	homozygous	115273934
12	17482073	17482074	G	A	31	GENIC	homozygous	115273936
12	17482465	17482466	A	G	27	GENIC	homozygous	115273938
12	17482496	17482497	T	C	22	GENIC	homozygous	115273940
12	17483298	17483299	C	T	26	GENIC	homozygous	115273942
12	17483666	17483667	A	C	28	GENIC	possibly homozygous	115273944
12	17483859	17483860	A	G	31	GENIC	homozygous	115273946
12	17483925	17483926	T	C	35	GENIC	homozygous	115273948
12	17484408	17484409	C	A	35	GENIC	homozygous	115273950
12	17484428	17484429	C	T	35	GENIC	homozygous	115273952
12	17485627	17485628	T	C	41	GENIC	homozygous	115273954
12	17485640	17485641	A	G	38	GENIC	homozygous	115273956
12	17485723	17485724	T	A	26	GENIC	homozygous	115273958
12	17486297	17486298	A	G	34	GENIC	homozygous	115273960