chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	27733358	27733359	C	G	27	GENIC	homozygous	111185100
17	27733436	27733437	A	C	13	GENIC	homozygous	111013630
17	27733723	27733724	A	G	31	GENIC	homozygous	111013632
17	27734029	27734030	C	G	26	GENIC	homozygous	111013634
17	27734417	27734418	G	A	47	GENIC	homozygous	111013636
17	27734513	27734514	T	C	35	GENIC	homozygous	111013638
17	27734938	27734939	T	A	34	GENIC	homozygous	111013640
17	27735085	27735086	A	G	47	GENIC	heterozygous	119451051
17	27735593	27735594	T	G	33	GENIC	homozygous	111013642
17	27735695	27735696	T	C	12	GENIC	homozygous	111013644
17	27736945	27736946	C	T	40	GENIC	homozygous	111013646
17	27737027	27737028	T	C	32	GENIC	homozygous	111013648
17	27737068	27737069	G	A	36	GENIC	homozygous	111013650
17	27737171	27737172	G	A	30	GENIC	homozygous	111013653
17	27737224	27737225	C	T	16	GENIC	homozygous	111013654
17	27738030	27738031	T	C	18	GENIC	homozygous	111013656
17	27738300	27738301	A	G	27	GENIC	homozygous	111013658
17	27738324	27738325	A	G	23	GENIC	homozygous	111013660
17	27738717	27738718	C	T	20	GENIC	homozygous	111013662
17	27735115	27735116	G	A	61	GENIC	heterozygous	119271551
17	27735283	27735284	G	A	7	GENIC	homozygous	119271553