chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	139476227	139476228	A	C	18	GENIC	homozygous	114250247
5	139476272	139476273	G	T	24	GENIC	homozygous	114250249
5	139476332	139476333	T	C	29	GENIC	homozygous	114250251
5	139476895	139476896	A	G	25	GENIC	homozygous	114250253
5	139477825	139477826	A	G	20	GENIC	homozygous	114250255
5	139479020	139479021	A	G	28	GENIC	homozygous	114028838
5	139480290	139480291	G	T	31	GENIC	homozygous	114028840
5	139483434	139483435	T	C	14	GENIC	homozygous	114250257
5	139486714	139486715	G	C	25	GENIC	homozygous	114250259
5	139489733	139489734	A	G	26	GENIC	homozygous	114250261
5	139489926	139489927	A	G	27	GENIC	homozygous	114028843
5	139490840	139490841	T	A	31	GENIC	homozygous	114250263
5	139494618	139494619	A	G	31	GENIC	homozygous	114028845
5	139496389	139496390	T	C	37	GENIC	homozygous	114028847
5	139496695	139496696	T	A	40	GENIC	possibly homozygous	114028848
5	139499202	139499203	A	C	17	GENIC	homozygous	114250265
5	139500148	139500149	G	A	19	GENIC	homozygous	114250267
5	139500337	139500338	A	G	10	GENIC	homozygous	114250269
5	139500649	139500650	A	G	9	GENIC	homozygous	114250271
5	139500752	139500753	C	T	16	GENIC	heterozygous	114028849
5	139501768	139501769	A	G	11	GENIC	homozygous	114250275
5	139502271	139502272	T	G	9	GENIC	homozygous	114028850
5	139502895	139502896	T	C	11	GENIC	homozygous	114028851
5	139504040	139504041	C	T	17	GENIC	homozygous	114028856
5	139504610	139504611	A	G	21	GENIC	homozygous	114028857
5	139504655	139504656	T	C	26	GENIC	homozygous	114028858