chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	44653389	44653415	ACAGGGCTCCTGGAAGGGCTAGGGCG		74	GENIC	homozygous	142201429
10	44655815	44655820	CAGGG		54	GENIC	homozygous	142201430
10	44656149	44656150	T	C	66	GENIC	homozygous	138782910
10	44656196	44656197	T	C	60	GENIC	homozygous	138782911
10	44656309	44656310	C	G	46	GENIC	homozygous	142238709
10	44657257	44657258	C	G	46	GENIC	homozygous	142238710
10	44657960	44657960		CA	44	GENIC	homozygous	138681865
10	44658093	44658094	T	C	66	GENIC	homozygous	138782912
10	44658597	44658598	T	C	57	GENIC	homozygous	142238711
10	44658637	44658638	G	A	56	GENIC	homozygous	142238712
10	44658916	44658917	G	A	51	GENIC	homozygous	154632116
10	44658916	44658917	G	T	51	GENIC	heterozygous	154632117
10	44660705	44660706	A	G	73	GENIC	homozygous	142238713
10	44660842	44660843	A	G	62	GENIC	homozygous	142238714
10	44660858	44660859	A	C	65	GENIC	homozygous	138782913
10	44661095	44661096	A	G	53	GENIC	homozygous	142238715
10	44662177	44662178	G	A	56	GENIC	homozygous	142238716
10	44662184	44662191	GGCTCAG		57	GENIC	homozygous	142201431
10	44662255	44662256	C	G	52	GENIC	homozygous	142238717
10	44662463	44662464	C	T	59	GENIC	homozygous	142238718
10	44662969	44662970	A	G	57	GENIC	homozygous	154632120
10	44663100	44663101	A	T	43	GENIC	homozygous	142238719
10	44664097	44664098	A	G	41	GENIC	homozygous	138782915
10	44664100	44664101	G	C	41	GENIC	homozygous	142238720
10	44664573	44664574	T	C	59	GENIC	homozygous	142238721
10	44666289	44666290	G	A	62	GENIC	homozygous	142238722
10	44668248	44668249	T	C	45	GENIC	homozygous	142238723
10	44668666	44668667	T	A	52	GENIC	homozygous	138782920
10	44669400	44669401	C	T	43	GENIC	homozygous	142238724
10	44669637	44669638	T	C	66	GENIC	homozygous	142238725
10	44676601	44676602	A	T	58	GENIC	homozygous	138782924
10	44677931	44677932	T	C	62	GENIC	homozygous	138782925
10	44662969	44662970	A		57	GENIC	heterozygous	403285227
10	44667795	44667796	C	A	24	GENIC	homozygous	403285228