chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	34102800	34102803	AGG		55	GENIC	homozygous	131105062
11	34103195	34103196	G		55	GENIC	homozygous	131105063
11	34104677	34104678	A	C	65	GENIC	homozygous	115819465
11	34105052	34105053	C	T	46	GENIC	homozygous	115819467
11	34106029	34106030	A	T	53	GENIC	homozygous	115819471
11	34106957	34106958	A	G	37	GENIC	homozygous	115819473
11	34107230	34107230		A	21	GENIC	heterozygous	131715961
11	34110201	34110202	T	C	56	GENIC	homozygous	115819477
11	34112673	34112674	A	G	46	GENIC	homozygous	115819479
11	34113842	34113843	T	C	65	GENIC	homozygous	115819481
11	34116001	34116002	A	G	68	GENIC	homozygous	115819485
11	34116172	34116173	A	G	50	GENIC	homozygous	118142812
11	34116420	34116421	A	G	48	GENIC	homozygous	115819487
11	34103477	34103478	T	C	72	GENIC	homozygous	116036475
11	34104503	34104504	T	C	43	GENIC	homozygous	116036477
11	34105823	34105824	C	G	51	GENIC	homozygous	116036479
11	34105844	34105845	C	T	54	GENIC	homozygous	116036481
11	34106027	34106028	G		52	GENIC	homozygous	128897877
11	34118259	34118260	T	C	45	GENIC	homozygous	115819491
11	34119380	34119381	C	G	42	GENIC	homozygous	115819493