chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	29701110	29701111	G	T	13	GENIC	homozygous	46238464
19	29701341	29701342	C	T	25	GENIC	homozygous	46238465
19	29701396	29701397	T	C	27	GENIC	homozygous	46238466
19	29701402	29701403	T	C	28	GENIC	homozygous	46238467
19	29701562	29701563	C	G	23	GENIC	homozygous	46238468
19	29701649	29701650	A	G	30	GENIC	homozygous	46238469
19	29701846	29701847	G	T	29	GENIC	homozygous	46238470
19	29701853	29701854	T	TCCGTA	26	GENIC	homozygous	46238471
19	29702179	29702180	C	CATGTGTGT	19	GENIC	heterozygous	46429256
19	29702638	29702639	A	C	32	GENIC	homozygous	46238473
19	29702933	29702934	G	A	32	GENIC	homozygous	46238474
19	29703195	29703196	A	C	36	GENIC	homozygous	46238475
19	29703321	29703322	G	T	25	GENIC	homozygous	46238476
19	29702179	29702180	C	CATGTGAGT	19	GENIC	possibly homozygous	46677316