chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10592748	10592749	T	C	9	GENIC	homozygous	46059340
19	10592826	10592827	C	T	7	GENIC	homozygous	46059341
19	10593333	10593334	A	G	7	GENIC	homozygous	46279838
19	10594152	10594153	C	T	15	GENIC	homozygous	46059345
19	10596356	10596357	G	A	15	GENIC	homozygous	46059348
19	10596493	10596496	AGG	---	10	GENIC	homozygous	46279839
19	10596517	10596518	C	T	13	GENIC	homozygous	46279840
19	10596627	10596628	C	G	24	GENIC	homozygous	46059349
19	10596954	10596955	C	G	20	GENIC	homozygous	46059351
19	10597306	10597307	T	C	7	GENIC	homozygous	46059352
19	10597405	10597406	T	C	19	GENIC	homozygous	46059353
19	10597665	10597666	T	C	8	GENIC	homozygous	46397392
19	10597666	10597667	C	T	8	GENIC	homozygous	46279841
19	10598858	10598859	T	A	13	GENIC	homozygous	46279842
19	10598860	10598861	T	G	13	GENIC	homozygous	46279843
19	10598962	10598963	A	G	16	GENIC	homozygous	46059354
19	10600234	10600235	C	G	12	GENIC	homozygous	46279844
19	10601397	10601398	G	GAA	8	GENIC	homozygous	46279845
19	10601477	10601478	C	-	9	GENIC	homozygous	46059362
19	10601525	10601526	A	G	11	GENIC	homozygous	46279846
19	10601735	10601736	G	A	10	GENIC	homozygous	46059365
19	10602658	10602659	G	GC	9	GENIC	homozygous	46279848
19	10603012	10603013	A	G	15	GENIC	homozygous	46059373
19	10603372	10603373	T	C	24	GENIC	homozygous	46059374
19	10603889	10603890	T	C	9	GENIC	homozygous	46059376
19	10604899	10604900	T	C	20	GENIC	homozygous	46059377
19	10605949	10605950	G	GC	10	GENIC	homozygous	46059380
19	10606467	10606468	T	TA	20	GENIC	homozygous	46059381
19	10606501	10606502	G	T	13	GENIC	homozygous	46279850
19	10606739	10606740	A	G	16	GENIC	homozygous	46279851