chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10572093	10572094	T	C	18	GENIC	homozygous	46059312
19	10572190	10572191	A	G	13	GENIC	homozygous	46279809
19	10572697	10572698	G	A	9	GENIC	homozygous	46279810
19	10572999	10573000	G	A	14	GENIC	homozygous	46279811
19	10573297	10573298	G	C	9	GENIC	homozygous	46059315
19	10573899	10573900	A	-	7	GENIC	homozygous	46059318
19	10574087	10574088	T	C	9	GENIC	homozygous	46059319
19	10574287	10574288	G	T	12	GENIC	homozygous	46059320
19	10574736	10574737	C	T	8	GENIC	homozygous	46279813
19	10575019	10575020	G	A	13	GENIC	homozygous	46059321
19	10575181	10575182	T	TA	10	GENIC	homozygous	46059322
19	10575382	10575383	A	-	8	GENIC	homozygous	46059323
19	10575789	10575790	C	A	12	GENIC	homozygous	46059325
19	10576360	10576361	C	G	11	GENIC	homozygous	46059328