chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52270929	52270930	G	A	2	GENIC	homozygous	119632696
19	52271010	52271011	T		6	GENIC	homozygous	132236318
19	52271017	52271018	T	A	6	GENIC	homozygous	124591345
19	52271247	52271248	C		18	GENIC	homozygous	132236319
19	52274803	52274804	G	A	24	GENIC	homozygous	109824655
19	52271589	52271590	G	A	20	GENIC	homozygous	109824647
19	52273402	52273403	G	T	28	GENIC	homozygous	109824649
19	52274299	52274300	T	C	22	GENIC	homozygous	109824651
19	52274457	52274458	A	G	24	GENIC	homozygous	109824653
19	52274816	52274817	A	C	25	GENIC	homozygous	109824657
19	52275436	52275437	A	G	19	GENIC	homozygous	109824659
19	52275767	52275767		T	19	GENIC	homozygous	132236320
19	52276553	52276554	A	G	24	GENIC	homozygous	109824661
19	52277331	52277332	C	T	20	GENIC	homozygous	109824663
19	52281065	52281066	C	G	28	GENIC	homozygous	109824665
19	52281698	52281699	T		24	GENIC	possibly homozygous	132236321
19	52281805	52281806	T	C	23	GENIC	homozygous	109824667
19	52281937	52281938	T	C	24	GENIC	homozygous	109824669
19	52282694	52282695	C	T	26	GENIC	homozygous	109824671
19	52282815	52282816	C	T	22	GENIC	homozygous	109824673
19	52278912	52278913	C	T	17	GENIC	homozygous	110014151