chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3310981	3310982	A	G	52	GENIC	homozygous	109068414
20	3311209	3311210	A	G	44	GENIC	homozygous	109068416
20	3312022	3312023	C	T	46	GENIC	homozygous	134903278
20	3312721	3312722	A	C	44	GENIC	homozygous	109068418
20	3312822	3312822		CGAGG	44	GENIC	homozygous	129650712
20	3312995	3312996	T	C	36	GENIC	homozygous	109605427
20	3313301	3313302	C	T	50	GENIC	homozygous	134903279
20	3314181	3314182	T	C	40	GENIC	homozygous	109068422
20	3314643	3314644	T	A	49	GENIC	homozygous	109370713
20	3314666	3314667	T	C	44	GENIC	homozygous	109490464
20	3314688	3314716	ATATATATATAAATAAATAAATAAATAA		42	GENIC	homozygous	129650713
20	3314717	3314718	T	C	41	GENIC	homozygous	109490466
20	3315067	3315067		AAAC	60	GENIC	homozygous	129650714
20	3315125	3315126	G	A	63	GENIC	homozygous	109068430
20	3315402	3315402		GGCCCCTCTC	54	GENIC	homozygous	134757840
20	3315404	3315404		CCCCTCACAC	50	GENIC	homozygous	134757841
20	3315681	3315682	G	A	32	GENIC	homozygous	109370715
20	3315725	3315726	A	C	38	GENIC	homozygous	109370717
20	3315796	3315797	C	T	22	GENIC	homozygous	109490470
20	3315820	3315820		GGGGCTGGGG	27	GENIC	heterozygous	134900674
20	3315821	3315821		TTTAGCTCAGTGGTAGAGCGCTTACCT	23	GENIC	heterozygous	134900675
20	3315891	3315892	G	A	24	GENIC	homozygous	109370719
20	3316212	3316213	C	A	54	GENIC	possibly homozygous	109068446
20	3317096	3317097	G	C	43	GENIC	homozygous	109068450
20	3317158	3317159	G	C	45	GENIC	homozygous	109068452
20	3317205	3317207	GC		34	GENIC	homozygous	131554514
20	3317209	3317212	GGC		34	GENIC	homozygous	131554515
20	3317287	3317288	C	T	55	GENIC	homozygous	109370721
20	3317295	3317296	G	A	59	GENIC	homozygous	109370723
20	3317389	3317392	ACG		52	GENIC	homozygous	129650715
20	3317476	3317479	GTC		42	GENIC	homozygous	134757842
20	3317694	3317695	T	C	51	GENIC	possibly homozygous	109068454
20	3317980	3317981	T	C	52	GENIC	homozygous	109068456
20	3319117	3319118	C	T	47	GENIC	homozygous	109370725