chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52270929	52270930	G	A	14	GENIC	possibly homozygous	119632696
19	52271589	52271590	G	A	45	GENIC	homozygous	109824647
19	52273402	52273403	G	T	46	GENIC	possibly homozygous	109824649
19	52274299	52274300	T	C	48	GENIC	homozygous	109824651
19	52274457	52274458	A	G	63	GENIC	homozygous	109824653
19	52274803	52274804	G	A	61	GENIC	homozygous	109824655
19	52274816	52274817	A	C	60	GENIC	homozygous	109824657
19	52275436	52275437	A	G	33	GENIC	possibly homozygous	109824659
19	52276553	52276554	A	G	64	GENIC	homozygous	109824661
19	52277331	52277332	C	T	58	GENIC	homozygous	109824663
19	52281065	52281066	C	G	43	GENIC	homozygous	109824665
19	52281805	52281806	T	C	33	GENIC	homozygous	109824667
19	52281937	52281938	T	C	38	GENIC	homozygous	109824669
19	52282694	52282695	C	T	40	GENIC	homozygous	109824671
19	52282815	52282816	C	T	35	GENIC	homozygous	109824673
19	52278912	52278913	C	T	39	GENIC	homozygous	110014151