chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	50090589	50090590	A	G	16	GENIC	homozygous	109725972
19	50090604	50090605	A	G	15	GENIC	homozygous	109725974
19	50090609	50090610	A	G	16	GENIC	homozygous	109725976
19	50090610	50090611	G	A	16	GENIC	homozygous	109725978
19	50090619	50090620	A	G	12	GENIC	homozygous	109725980
19	50090620	50090621	G	A	13	GENIC	homozygous	109725982
19	50110874	50110875	T	C	11	GENIC	homozygous	109788434
19	50110877	50110878	T	C	12	GENIC	homozygous	109788436
19	50112795	50112796	T	G	18	GENIC	homozygous	109788438
19	50112798	50112799	T	A	18	GENIC	homozygous	109788440
19	50112830	50112831	C	G	24	GENIC	homozygous	109788442
19	50112880	50112881	G	A	26	GENIC	homozygous	109726044
19	50112886	50112887	G	A	27	GENIC	homozygous	109726046
19	50112890	50112891	C	A	27	GENIC	homozygous	109726048
19	50112900	50112901	T	A	24	GENIC	homozygous	109726050
19	50112911	50112912	G	A	21	GENIC	homozygous	109726052
19	50112917	50112918	G	C	18	GENIC	homozygous	109726054
19	50116322	50116323	C	A	24	GENIC	homozygous	109788444
19	50165407	50165408	G	C	5	GENIC	homozygous	109726305