chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10572093	10572094	T	C	20	GENIC	homozygous	46059312
19	10572350	10572351	C	T	20	GENIC	homozygous	46059313
19	10573115	10573116	C	A	19	GENIC	possibly homozygous	46059314
19	10573297	10573298	G	C	21	GENIC	possibly homozygous	46059315
19	10573355	10573356	T	A	18	GENIC	homozygous	46059316
19	10573410	10573411	C	G	24	GENIC	possibly homozygous	46059317
19	10573899	10573900	A	-	10	GENIC	possibly homozygous	46059318
19	10574087	10574088	T	C	19	GENIC	homozygous	46059319
19	10574287	10574288	G	T	13	GENIC	possibly homozygous	46059320
19	10575019	10575020	G	A	16	GENIC	homozygous	46059321
19	10575181	10575182	T	TA	17	GENIC	homozygous	46059322
19	10575567	10575590	CTCCCTCCCTCCCTCCCTCCCTC	-----------------------	2	GENIC	heterozygous	46059324
19	10575565	10575566	C	-	2	GENIC	heterozygous	46458603
19	10575789	10575790	C	A	5	GENIC	homozygous	46059325
19	10576360	10576361	C	G	7	GENIC	possibly homozygous	46059328