chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71400381	71400382	G	C	24	GENIC	homozygous	118195470
11	71401474	71401475	C	T	46	GENIC	homozygous	115984506
11	71402518	71402519	A	G	51	GENIC	homozygous	115984508
11	71403299	71403300	T	C	53	GENIC	homozygous	115984510
11	71406291	71406291		CCTTTC	43	GENIC	homozygous	131108268
11	71406994	71407009	TAAAACAAAACAAAA		46	GENIC	homozygous	131108269
11	71407635	71407636	C	G	52	GENIC	homozygous	115984512
11	71407802	71407803	T	A	58	GENIC	homozygous	115984514
11	71407850	71407851	G	A	52	GENIC	homozygous	115984516
11	71409114	71409115	T		45	GENIC	homozygous	131108270
11	71410956	71410957	T	A	24	GENIC	homozygous	115984518
11	71411219	71411220	C	T	55	GENIC	homozygous	115984520
11	71412603	71412604	G	A	45	GENIC	homozygous	115984522
11	71413926	71413927	A	G	54	GENIC	homozygous	115984524
11	71414083	71414084	T		38	GENIC	homozygous	131716855
11	71414370	71414371	A	G	51	GENIC	homozygous	115984526
11	71414714	71414715	T	G	44	GENIC	possibly homozygous	115984528
11	71415858	71415860	TG		30	GENIC	homozygous	131108271
11	71416323	71416324	T	A	50	GENIC	homozygous	115984530
11	71416586	71416586		ATATACTGAGACAAACTGATAAA	51	GENIC	homozygous	131108272
11	71417004	71417005	T	C	38	GENIC	homozygous	115984532
11	71418033	71418034	C	T	21	GENIC	homozygous	118216071
11	71419020	71419021	T	C	34	GENIC	homozygous	116110550
11	71414084	71414085	A	C	52	GENIC	homozygous	131719339
11	71407392	71407393	C	T	57	GENIC	homozygous	116354833