chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	54060294	54060295	C		8	GENIC	homozygous	130703603
16	54060296	54060297	G	C	8	GENIC	homozygous	112220858
16	54060301	54060302	G	A	8	GENIC	homozygous	112220859
16	54060303	54060304	G		8	GENIC	homozygous	130703604
16	54060317	54060318	C		8	GENIC	homozygous	130703605
16	54060332	54060333	A		6	GENIC	homozygous	130703606
16	54060340	54060340		AG	6	GENIC	homozygous	130703607
16	54060342	54060343	G	A	5	GENIC	homozygous	130705660
16	54060307	54060308	C	G	8	GENIC	homozygous	130705657
16	54060308	54060309	G	C	8	GENIC	homozygous	130705658
16	54060312	54060313	C	G	8	GENIC	homozygous	130705659
16	54060345	54060347	TC		3	GENIC	homozygous	130703608
16	54060420	54060421	G	T	13	GENIC	homozygous	111985075
16	54085590	54085590		T	14	GENIC	homozygous	129366493
16	54085600	54085601	T		15	GENIC	homozygous	129366494
16	54085656	54085656		GGA	7	GENIC	homozygous	129366496
16	54085675	54085676	A		8	GENIC	homozygous	129366497
16	54085721	54085722	G		13	GENIC	homozygous	129366498
16	54092691	54092692	A		27	GENIC	heterozygous	130703609
16	54097948	54097949	T	G	33	GENIC	possibly homozygous	111825638
16	54126979	54126980	G	A	34	GENIC	heterozygous	124231048
16	54126979	54126979		A	34	GENIC	heterozygous	130159194
16	54127021	54127022	T	C	30	GENIC	heterozygous	119119203
16	54085671	54085672	A	G	8	GENIC	homozygous	112131539
16	54085680	54085681	A	G	8	GENIC	homozygous	119166852
16	54126988	54126989	T	C	33	GENIC	heterozygous	119166858
16	54126989	54126990	G	A	33	GENIC	heterozygous	119166860