chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	5625485	5625485		G	49	GENIC	homozygous	127846243
3	5626244	5626245	C	G	67	GENIC	homozygous	119965318
3	5628500	5628501	T	C	72	GENIC	homozygous	111438970
3	5628567	5628568	G	A	66	GENIC	homozygous	119965320
3	5630335	5630336	T	C	71	GENIC	homozygous	111438971
3	5630803	5630804	T	C	52	GENIC	possibly homozygous	111438972
3	5631500	5631501	G	A	58	GENIC	homozygous	111438973
3	5631604	5631605	T	A	64	GENIC	homozygous	111438974
3	5632302	5632303	G	A	62	GENIC	homozygous	119965322
3	5632669	5632670	T	C	40	GENIC	homozygous	111438975
3	5633287	5633288	G	T	72	GENIC	homozygous	111438976
3	5633858	5633859	A	G	60	GENIC	possibly homozygous	111438977
3	5635134	5635135	T	C	35	GENIC	homozygous	111438979
3	5635442	5635448	GTTTGG		38	GENIC	homozygous	127846244
3	5635661	5635662	A	G	44	GENIC	homozygous	111438980
3	5636000	5636001	A	G	52	GENIC	homozygous	119965324
3	5637750	5637751	C	T	64	GENIC	homozygous	119965326
3	5640197	5640198	A	G	51	GENIC	homozygous	111438991
3	5641424	5641425	G	C	7	GENIC	heterozygous	131840080
3	5645468	5645469	G	A	52	GENIC	homozygous	119965328
3	5646390	5646391	C	A	58	GENIC	homozygous	119965330
3	5646499	5646500	T	A	46	GENIC	homozygous	111439004
3	5647408	5647409	T	C	50	GENIC	homozygous	111439005
3	5647467	5647468	T	G	48	GENIC	heterozygous	127968036
3	5647965	5647966	T	C	23	GENIC	homozygous	111439006
3	5648000	5648002	GT		28	GENIC	homozygous	127846247
3	5648236	5648237	C	T	51	GENIC	homozygous	119965332
3	5649843	5649844	A	G	49	GENIC	homozygous	111439010
3	5654639	5654640	C	A	54	GENIC	homozygous	119965334