chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	53752745	53752746	A	G	55	GENIC	heterozygous	118451340
13	53752861	53752862	T	C	45	GENIC	heterozygous	115010144
13	53752862	53752863	G	C	45	GENIC	heterozygous	115010146
13	53752865	53752866	G	T	46	GENIC	heterozygous	115010148
13	53752874	53752875	G	A	48	GENIC	heterozygous	115010150
13	53752875	53752876	G	A	49	GENIC	heterozygous	115010152
13	53752879	53752880	T	A	43	GENIC	heterozygous	115010154
13	53752882	53752883	G	A	39	GENIC	heterozygous	115010156
13	53752925	53752926	C	T	65	GENIC	heterozygous	115010164
13	53752933	53752934	G	A	69	GENIC	heterozygous	115198856
13	53752946	53752947	C	A	70	GENIC	heterozygous	114349567
13	53752953	53752954	C	G	69	GENIC	heterozygous	114349569
13	53752954	53752955	A	G	68	GENIC	heterozygous	114349571
13	53752975	53752976	A	C	65	GENIC	heterozygous	114349573
13	53752992	53752993	A	T	61	GENIC	heterozygous	114349575
13	53752995	53752996	A	G	58	GENIC	heterozygous	114349577
13	53753015	53753016	C	T	49	GENIC	heterozygous	114949156
13	53773953	53773954	A	G	41	GENIC	heterozygous	118592155
13	53777164	53777165	A	G	176	GENIC	heterozygous	118498899
13	53824967	53824968	T	C	41	GENIC	heterozygous	114349723
13	53841390	53841391	C	A	187	GENIC	heterozygous	118542288
13	53841471	53841472	A	C	32	GENIC	heterozygous	118498900
13	53862933	53862934	G	C	18	GENIC	homozygous	118451367
13	53862966	53862967	T	A	40	GENIC	homozygous	115010168
13	53863777	53863778	T	G	32	GENIC	possibly homozygous	114349839