chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54078097	54078098	A	C	5	GENIC	homozygous	46381464
19	54078338	54078339	T	-	5	GENIC	heterozygous	46492814
19	54078456	54078457	T	-	5	GENIC	homozygous	46163601
19	54078582	54078583	G	A	24	GENIC	possibly homozygous	46492816
19	54079420	54079421	G	C	12	GENIC	homozygous	46163606
19	54080342	54080343	T	C	11	GENIC	homozygous	46492818
19	54080878	54080879	A	G	17	GENIC	homozygous	46163611
19	54081038	54081039	C	CCAGA	5	GENIC	heterozygous	46163613
19	54081415	54081416	A	G	21	GENIC	possibly homozygous	46163614
19	54081721	54081722	A	G	15	GENIC	possibly homozygous	46163615
19	54083518	54083519	C	A	16	GENIC	possibly homozygous	46163619
19	54083793	54083794	C	-	12	GENIC	heterozygous	46163620
19	54087686	54087687	C	A	12	GENIC	possibly homozygous	46163628
19	54089441	54089442	A	G	24	GENIC	possibly homozygous	46163631
19	54089853	54089854	C	T	32	GENIC	possibly homozygous	46296581
19	54083584	54083585	C	T	12	GENIC	homozygous	46296578
19	54084106	54084107	T	C	4	GENIC	heterozygous	46296579
19	54084167	54084168	A	T	10	GENIC	homozygous	46296580
19	54090761	54090762	C	T	12	GENIC	homozygous	46262759
19	54091174	54091175	G	T	21	GENIC	possibly homozygous	46163635
19	54091298	54091299	A	G	23	GENIC	possibly homozygous	46163636
19	54091467	54091468	A	-	2	GENIC	homozygous	46163637
19	54093158	54093159	A	G	16	GENIC	homozygous	46163653
19	54094474	54094475	G	A	17	GENIC	homozygous	46262764
19	54096888	54096889	T	C	23	GENIC	homozygous	46163664
19	54097524	54097525	A	AC	7	GENIC	homozygous	46296583
19	54097619	54097620	T	C	15	GENIC	homozygous	46163669
19	54098948	54098949	T	C	37	GENIC	heterozygous	46262768
19	54098957	54098958	G	T	32	GENIC	heterozygous	46262769