chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	56242961	56242962	A	T	49	GENIC	homozygous	143585506
13	56243453	56243453		C	31	GENIC	homozygous	143550929
13	56245023	56245024	G	A	34	GENIC	homozygous	143585507
13	56245080	56245081	G	C	40	GENIC	homozygous	143585508
13	56245868	56245869	G	T	45	GENIC	homozygous	139308071
13	56244965	56244966	G	T	32	GENIC	possibly homozygous	139308068
13	56245160	56245161	T	G	51	GENIC	homozygous	139308069
13	56245708	56245709	T	G	73	GENIC	homozygous	139308070
13	56246114	56246115	G	A	56	GENIC	homozygous	139308072
13	56247031	56247032	G	C	51	GENIC	homozygous	139308073
13	56247579	56247579		CTCTCC	10	GENIC	heterozygous	145152160
13	56248847	56248848	T	C	51	GENIC	homozygous	139308074
13	56247538	56247538		TC	8	GENIC	homozygous	139176189
13	56250440	56250441	A	T	55	GENIC	homozygous	139308075
13	56250842	56250842		T	60	GENIC	homozygous	139176193
13	56251720	56251720		A	40	GENIC	homozygous	142346222
13	56254421	56254422	T	C	49	GENIC	homozygous	139308078
13	56260351	56260352	C	T	41	GENIC	homozygous	139308081
13	56256134	56256135	T	A	47	GENIC	homozygous	143585509
13	56257162	56257163	A	T	47	GENIC	homozygous	143585510
13	56257205	56257206	G	A	44	GENIC	homozygous	139308079
13	56258021	56258022	G	A	36	GENIC	homozygous	143585511
13	56260296	56260297	C	T	47	GENIC	homozygous	143585512
13	56250662	56250662		C	17	GENIC	homozygous	144100647
13	56260739	56260740	C	G	45	GENIC	homozygous	139308082
13	56261346	56261347	T	C	47	GENIC	homozygous	139308083
13	56262726	56262726		T	49	GENIC	homozygous	139176197
13	56265434	56265435	G	A	53	GENIC	possibly homozygous	139308084
13	56265583	56265584	T		51	GENIC	homozygous	139176198
13	56265846	56265847	T	C	45	GENIC	homozygous	143585513
13	56262028	56262029	T	G	43	GENIC	homozygous	154814492
13	56262028	56262029	T		43	GENIC	heterozygous	403339652