chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62141111	62141112	A	G	25	GENIC	homozygous	116613384
10	62144667	62144668	T	A	19	GENIC	homozygous	116939603
10	62145534	62145535	G	A	23	GENIC	homozygous	116613390
10	62147302	62147303	G	A	38	GENIC	homozygous	116939605
10	62147828	62147829	A	G	22	GENIC	homozygous	116613394
10	62148443	62148444	T	C	24	GENIC	homozygous	116613396
10	62149393	62149394	A	C	22	GENIC	heterozygous	117104186
10	62149953	62149954	A	T	25	GENIC	homozygous	116790933
10	62150298	62150299	C	T	18	GENIC	homozygous	116939607
10	62151565	62151566	T	C	34	GENIC	homozygous	116790935
10	62158419	62158420	C	T	23	GENIC	homozygous	116613420
10	62163083	62163084	T	C	16	GENIC	homozygous	116613426
10	62164836	62164837	T	A	12	GENIC	homozygous	116790939
10	62176606	62176607	C	A	36	GENIC	homozygous	116790941
10	62179861	62179862	C	T	27	GENIC	homozygous	116790943
10	62180122	62180123	T	C	24	GENIC	possibly homozygous	116613450
10	62186171	62186172	T	C	13	GENIC	homozygous	117104188
10	62189330	62189331	T	A	14	GENIC	homozygous	116613486