chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62675916	62675917	T	C	24	GENIC	homozygous	116614089
10	62677107	62677108	C	T	33	GENIC	homozygous	116890994
10	62677258	62677259	T	C	20	GENIC	homozygous	116890996
10	62678465	62678466	A	G	13	GENIC	homozygous	116614099
10	62680373	62680374	A	C	24	GENIC	homozygous	116891002
10	62681259	62681260	C	T	20	GENIC	homozygous	116891004
10	62683141	62683142	C	T	21	GENIC	homozygous	116939775
10	62683980	62683981	T	C	27	GENIC	homozygous	116891008
10	62684242	62684243	G	A	28	GENIC	homozygous	116891010
10	62684453	62684454	C	T	39	GENIC	homozygous	116939777
10	62684523	62684524	C	T	41	GENIC	homozygous	116891012
10	62686412	62686413	G	A	19	GENIC	homozygous	116891014
10	62686554	62686555	G	A	20	GENIC	homozygous	116891016
10	62686982	62686983	A	G	31	GENIC	homozygous	116891018
10	62687782	62687783	C	T	32	GENIC	homozygous	116891020
10	62689217	62689218	A	G	19	GENIC	homozygous	116891024
10	62689920	62689921	C	T	11	GENIC	homozygous	116891028
10	62691414	62691415	T	C	20	GENIC	homozygous	116614111
10	62691419	62691420	G	A	21	GENIC	homozygous	116891030
10	62691868	62691869	G	A	21	GENIC	homozygous	116891032