chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71401474	71401475	C	T	12	GENIC	homozygous	115984506
11	71402518	71402519	A	G	46	GENIC	homozygous	115984508
11	71403299	71403300	T	C	34	GENIC	homozygous	115984510
11	71407392	71407393	C	T	58	GENIC	homozygous	116354833
11	71407635	71407636	C	G	30	GENIC	homozygous	115984512
11	71407802	71407803	T	A	14	GENIC	homozygous	115984514
11	71407850	71407851	G	A	32	GENIC	homozygous	115984516
11	71410956	71410957	T	A	18	GENIC	homozygous	115984518
11	71411219	71411220	C	T	17	GENIC	homozygous	115984520
11	71412603	71412604	G	A	44	GENIC	homozygous	115984522
11	71413926	71413927	A	G	11	GENIC	homozygous	115984524
11	71414714	71414715	T	G	24	GENIC	homozygous	115984528
11	71416323	71416324	T	A	28	GENIC	homozygous	115984530
11	71417004	71417005	T	C	45	GENIC	homozygous	115984532
11	71417287	71417288	G	A	22	GENIC	homozygous	116361245