chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62141111	62141112	A	G	24	GENIC	homozygous	116613384
10	62144667	62144668	T	A	23	GENIC	homozygous	116939603
10	62145534	62145535	G	A	14	GENIC	homozygous	116613390
10	62147302	62147303	G	A	19	GENIC	homozygous	116939605
10	62147828	62147829	A	G	26	GENIC	homozygous	116613394
10	62148443	62148444	T	C	23	GENIC	homozygous	116613396
10	62149953	62149954	A	T	30	GENIC	homozygous	116790933
10	62150298	62150299	C	T	15	GENIC	homozygous	116939607
10	62151565	62151566	T	C	51	GENIC	homozygous	116790935
10	62158419	62158420	C	T	28	GENIC	homozygous	116613420
10	62163083	62163084	T	C	25	GENIC	homozygous	116613426
10	62164836	62164837	T	A	20	GENIC	homozygous	116790939
10	62176606	62176607	C	A	23	GENIC	homozygous	116790941
10	62179861	62179862	C	T	34	GENIC	possibly homozygous	116790943
10	62180122	62180123	T	C	29	GENIC	homozygous	116613450
10	62185722	62185723	A	G	39	GENIC	possibly homozygous	117997323
10	62186171	62186172	T	C	16	GENIC	homozygous	117104188
10	62186229	62186230	T	C	18	GENIC	homozygous	117997326
10	62189330	62189331	T	A	25	GENIC	homozygous	116613486
10	62185789	62185790	G	T	31	GENIC	heterozygous	118075076
10	62163980	62163981	C	A	16	GENIC	possibly homozygous	116978454
10	62181396	62181397	C	T	22	GENIC	heterozygous	118075075