chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52625558	52625559	A	G	8	GENIC	homozygous	114550618
13	52626854	52626855	C	A	11	GENIC	homozygous	114550619
13	52629060	52629061	T	C	23	GENIC	homozygous	114550621
13	52630313	52630314	G	A	22	GENIC	homozygous	114550622
13	52630886	52630887	C	T	14	GENIC	homozygous	114550623
13	52630911	52630912	T	C	17	GENIC	homozygous	114550624
13	52631073	52631074	C	T	18	GENIC	homozygous	114550625
13	52631367	52631368	A	G	12	GENIC	homozygous	114550626
13	52631369	52631370	G	A	10	GENIC	homozygous	114550627
13	52631523	52631524	G	A	14	GENIC	homozygous	114617560
13	52631527	52631528	G	C	14	GENIC	homozygous	114550628
13	52631581	52631582	C	T	23	GENIC	homozygous	114550629
13	52631905	52631906	T	C	18	GENIC	homozygous	114550630
13	52632042	52632043	C	T	21	GENIC	homozygous	114550631
13	52632559	52632560	T	C	15	GENIC	homozygous	114617562
13	52632881	52632882	T	C	15	GENIC	possibly homozygous	114550632
13	52633346	52633347	C	T	32	GENIC	homozygous	114550633
13	52633428	52633429	T	G	22	GENIC	homozygous	114550634
13	52633515	52633516	G	A	22	GENIC	homozygous	114550635
13	52634009	52634010	C	T	14	GENIC	homozygous	114550636
13	52634122	52634123	G	A	16	GENIC	homozygous	114550637
13	52634142	52634143	A	G	12	GENIC	homozygous	114550638
13	52634155	52634156	C	T	16	GENIC	homozygous	114550639
13	52634177	52634178	T	G	13	GENIC	homozygous	114550640
13	52634237	52634238	A	G	16	GENIC	homozygous	114550641
13	52634760	52634761	T	A	24	GENIC	homozygous	114550642
13	52636082	52636083	T	C	20	GENIC	homozygous	114550644
13	52636752	52636753	T	C	20	GENIC	homozygous	114550645
13	52636882	52636883	A	G	13	GENIC	homozygous	114550646