chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	34101714	34101715	G	A	50	GENIC	homozygous	115819459
11	34103747	34103748	G	A	54	GENIC	homozygous	115819461
11	34104558	34104559	C	T	47	GENIC	homozygous	115819463
11	34104677	34104678	A	C	56	GENIC	homozygous	115819465
11	34105052	34105053	C	T	36	GENIC	homozygous	115819467
11	34105606	34105607	T	C	47	GENIC	homozygous	115819469
11	34106029	34106030	A	T	49	GENIC	homozygous	115819471
11	34106957	34106958	A	G	46	GENIC	homozygous	115819473
11	34107680	34107681	C	T	39	GENIC	homozygous	115819475
11	34110201	34110202	T	C	69	GENIC	homozygous	115819477
11	34112673	34112674	A	G	62	GENIC	homozygous	115819479
11	34113842	34113843	T	C	62	GENIC	homozygous	115819481
11	34115551	34115552	C	T	55	GENIC	homozygous	115819483
11	34116001	34116002	A	G	59	GENIC	homozygous	115819485
11	34116420	34116421	A	G	64	GENIC	homozygous	115819487
11	34118250	34118251	C	T	46	GENIC	homozygous	115819489
11	34118259	34118260	T	C	47	GENIC	homozygous	115819491
11	34106027	34106028	G		50	GENIC	possibly homozygous	128897877
11	34113368	34113373	AGAGA		53	GENIC	homozygous	128897878
11	34116172	34116173	A	G	62	GENIC	homozygous	118142812
11	34119380	34119381	C	G	55	GENIC	homozygous	115819493
11	34120381	34120382	G	C	48	GENIC	possibly homozygous	115819495
11	34120968	34120969	T	C	53	GENIC	homozygous	115819497