chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	34101995	34101996	C	A	41	GENIC	homozygous	116352653
11	34102837	34102838	G	A	65	GENIC	homozygous	116352654
11	34103102	34103103	G	A	43	GENIC	homozygous	116352655
11	34104677	34104678	A	C	45	GENIC	homozygous	115819465
11	34105052	34105053	C	T	46	GENIC	homozygous	115819467
11	34105606	34105607	T	C	57	GENIC	possibly homozygous	115819469
11	34105792	34105793	C	T	44	GENIC	homozygous	116352656
11	34106029	34106030	A	T	58	GENIC	homozygous	115819471
11	34106072	34106073	C	T	57	GENIC	homozygous	116352657
11	34106075	34106076	G	T	56	GENIC	homozygous	116352658
11	34106957	34106958	A	G	45	GENIC	homozygous	115819473
11	34108672	34108673	A	G	56	GENIC	homozygous	116352659
11	34103111	34103113	TG		43	GENIC	homozygous	131715960
11	34107230	34107230		A	28	GENIC	possibly homozygous	131715961
11	34105823	34105824	C	G	50	GENIC	homozygous	116036479
11	34109799	34109800	G	T	48	GENIC	homozygous	116099129
11	34110201	34110202	T	C	58	GENIC	homozygous	115819477
11	34112673	34112674	A	G	46	GENIC	homozygous	115819479
11	34113511	34113512	C	T	48	GENIC	homozygous	116352660
11	34113646	34113647	C	T	53	GENIC	homozygous	116352661
11	34113842	34113843	T	C	39	GENIC	homozygous	115819481
11	34114577	34114578	G	T	59	GENIC	homozygous	116352662
11	34114682	34114683	C	A	48	GENIC	homozygous	116352663
11	34115676	34115677	C	T	41	GENIC	homozygous	116352664
11	34116001	34116002	A	G	50	GENIC	homozygous	115819485
11	34116420	34116421	A	G	57	GENIC	homozygous	115819487
11	34117924	34117925	C	T	50	GENIC	homozygous	116352665
11	34118259	34118260	T	C	58	GENIC	homozygous	115819491
11	34118902	34118902		CACCTCCACCTCCACCACCTCCACCTCCACCTCCACCACCACCTA	19	GENIC	possibly homozygous	133425905
11	34119380	34119381	C	G	54	GENIC	homozygous	115819493
11	34106027	34106028	G		58	GENIC	homozygous	128897877
11	34116172	34116173	A	G	50	GENIC	homozygous	118142812