chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	44658642	44658643	T	C	16	GENIC	homozygous	116582638
10	44658952	44658953	C	G	15	GENIC	homozygous	116582640
10	44659013	44659014	A	G	7	GENIC	homozygous	116582642
10	44659222	44659223	G	A	11	GENIC	homozygous	116770867
10	44659556	44659557	C	T	17	GENIC	possibly homozygous	116770871
10	44659724	44659725	G	C	12	GENIC	homozygous	116770873
10	44659973	44659974	C	T	14	GENIC	homozygous	117077971
10	44660177	44660178	C	T	12	GENIC	homozygous	117077972
10	44660190	44660191	G	T	14	GENIC	homozygous	116582660
10	44660614	44660615	T	G	9	GENIC	homozygous	116770875
10	44660618	44660619	A	G	9	GENIC	homozygous	116582664
10	44660788	44660789	A	G	20	GENIC	homozygous	116582666
10	44660802	44660803	A	G	26	GENIC	homozygous	117077973
10	44661057	44661058	A	C	18	GENIC	homozygous	116770881
10	44661337	44661338	C	T	28	GENIC	homozygous	116770883
10	44661356	44661357	A	G	25	GENIC	possibly homozygous	116770885
10	44661687	44661688	G	A	15	GENIC	possibly homozygous	117077974
10	44661841	44661842	A	C	18	GENIC	homozygous	116770887
10	44662663	44662664	T	A	66	GENIC	heterozygous	117992642
10	44662955	44662956	T	C	36	GENIC	heterozygous	118036086