chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	54005570	54005571	T	A	22	GENIC	homozygous	65114235
15	54006031	54006032	G	A	19	GENIC	homozygous	66067546
15	54006384	54006385	T	G	27	GENIC	homozygous	65114237
15	54006710	54006711	A	C	36	GENIC	homozygous	65566786
15	54007550	54007551	G	A	9	GENIC	homozygous	65566787
15	54007997	54007998	C	T	61	GENIC	possibly homozygous	65566788
15	54008163	54008164	C	T	56	GENIC	homozygous	65566789
15	54008420	54008421	C	A	42	GENIC	homozygous	65566790
15	54008969	54008970	T	C	29	GENIC	homozygous	65566791
15	54009909	54009910	A	C	34	GENIC	homozygous	65566792
15	54009910	54009911	G	T	34	GENIC	homozygous	65566793
15	54010257	54010258	A	G	15	GENIC	homozygous	65114243
15	54011844	54011845	G	A	31	GENIC	homozygous	65566794
15	54012186	54012187	G	A	40	GENIC	homozygous	65566795
15	54012485	54012486	C	T	22	GENIC	homozygous	65114245
15	54012769	54012770	C	T	31	GENIC	homozygous	65566796
15	54012846	54012847	T	C	29	GENIC	homozygous	65566797
15	54012922	54012923	C	T	28	GENIC	homozygous	65566798
15	54014361	54014362	G	A	20	GENIC	homozygous	65114247
15	54015224	54015225	T	C	18	GENIC	homozygous	65114250
15	54015571	54015572	C	T	28	GENIC	homozygous	65566799
15	54015803	54015804	T	C	19	GENIC	homozygous	65114253
15	54016014	54016015	C	T	22	GENIC	homozygous	65566800
15	54014562	54014563	T	C	17	GENIC	homozygous	65969760
15	54014563	54014564	C	A	17	GENIC	homozygous	84112619
15	54016665	54016666	A	T	29	GENIC	homozygous	65114257
15	54021071	54021072	C	T	25	GENIC	homozygous	65114264
15	54023586	54023587	C	T	26	GENIC	homozygous	65566801
15	54024095	54024096	A	G	24	GENIC	homozygous	65114269
15	54024254	54024255	G	A	40	GENIC	homozygous	65566802
15	54024271	54024272	T	G	38	GENIC	homozygous	65566803
15	54024436	54024437	G	C	31	GENIC	homozygous	65566804
15	54024983	54024984	T	C	22	GENIC	homozygous	65566805
15	54025907	54025908	C	T	20	GENIC	homozygous	65114272
15	54026803	54026804	A	T	22	GENIC	homozygous	65114273
15	54026806	54026807	A	T	24	GENIC	possibly homozygous	65566806