chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	34102470	34102471	T	G	27	GENIC	homozygous	116099121
11	34103437	34103437		AA	12	GENIC	homozygous	131907972
11	34105052	34105053	C	T	22	GENIC	homozygous	115819467
11	34103477	34103478	T	C	13	GENIC	homozygous	116036475
11	34104677	34104678	A	C	15	GENIC	homozygous	115819465
11	34104870	34104871	G	A	23	GENIC	homozygous	116099123
11	34106957	34106958	A	G	20	GENIC	homozygous	115819473
11	34107745	34107746	G	A	23	GENIC	possibly homozygous	116099125
11	34108468	34108469	A	C	17	GENIC	homozygous	116099127
11	34109799	34109800	G	T	18	GENIC	homozygous	116099129
11	34110201	34110202	T	C	21	GENIC	homozygous	115819477
11	34110583	34110584	C	A	18	GENIC	homozygous	116099131
11	34112673	34112674	A	G	20	GENIC	homozygous	115819479
11	34113030	34113040	TGTGTGTGCC		21	GENIC	homozygous	131907973
11	34113842	34113843	T	C	13	GENIC	homozygous	115819481
11	34116001	34116002	A	G	22	GENIC	homozygous	115819485
11	34116172	34116173	A	G	18	GENIC	homozygous	118142812
11	34116420	34116421	A	G	16	GENIC	homozygous	115819487
11	34118259	34118260	T	C	19	GENIC	homozygous	115819491
11	34118820	34118826	CCACCA		19	GENIC	homozygous	131907974
11	34118854	34118875	CACCTACACCACCACCTCCAA		19	GENIC	homozygous	131907975
11	34119380	34119381	C	G	12	GENIC	homozygous	115819493
11	34119852	34119853	C		14	GENIC	homozygous	131907976
11	34119856	34119857	C		15	GENIC	homozygous	131907977
11	34119861	34119870	CTGCTGTAG		16	GENIC	homozygous	131907978