chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	69391949	69391950	T	C	46	GENIC	homozygous	111083780
17	69393908	69393909	A	G	44	GENIC	homozygous	111212133
17	69394455	69394456	A	C	30	GENIC	homozygous	111083784
17	69395480	69395481	A	T	48	GENIC	homozygous	111083786
17	69398672	69398673	A	G	44	GENIC	homozygous	111083790
17	69407073	69407074	C	T	36	GENIC	heterozygous	111212134
17	69420772	69420773	T	C	41	GENIC	homozygous	111083812
17	69421883	69421884	G	A	4	GENIC	homozygous	111323076
17	69422173	69422174	T	A	54	GENIC	heterozygous	119395740
17	69410351	69410352	A	G	5	GENIC	heterozygous	119299496
17	69422095	69422096	T	A	86	GENIC	heterozygous	119395734
17	69422126	69422127	T	C	73	GENIC	heterozygous	119395736
17	69422130	69422131	G	A	68	GENIC	heterozygous	119395738
17	69423066	69423067	C	A	34	GENIC	possibly homozygous	119395742
17	69423225	69423226	G	A	46	GENIC	possibly homozygous	119395744
17	69428212	69428213	C	G	42	GENIC	homozygous	119299500
17	69429277	69429278	T	A	33	GENIC	heterozygous	119299502
17	69429882	69429883	C	A	34	GENIC	homozygous	119395746
17	69430091	69430092	T	A	43	GENIC	homozygous	111083814