chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	47641573	47641574	C	T	24	GENIC	homozygous	111057584
17	47643049	47643050	G	A	6	GENIC	homozygous	111057585
17	47644088	47644089	T	C	31	GENIC	homozygous	111057586
17	47644351	47644352	C	T	10	GENIC	homozygous	111057587
17	47644664	47644665	T	G	43	GENIC	homozygous	111245371
17	47645231	47645232	G	C	35	GENIC	homozygous	111057588
17	47646127	47646128	G	A	14	GENIC	homozygous	111057589
17	47648106	47648107	G	A	35	GENIC	homozygous	111057590
17	47648546	47648547	A	G	34	GENIC	homozygous	111057591
17	47648756	47648757	A	C	31	GENIC	heterozygous	111057592
17	47649968	47649969	T	C	7	GENIC	homozygous	111057593
17	47650726	47650727	T	C	12	GENIC	homozygous	119291074
17	47650774	47650775	A	G	14	GENIC	homozygous	119291075
17	47650803	47650804	T	G	14	GENIC	homozygous	119291076
17	47650863	47650864	G	A	29	GENIC	homozygous	119291077
17	47652123	47652124	G	A	5	GENIC	homozygous	119291078
17	47653741	47653742	T	A	35	GENIC	heterozygous	119364732
17	47653793	47653794	T	G	39	GENIC	heterozygous	119291081
17	47653800	47653801	A	G	34	GENIC	heterozygous	119291082
17	47653733	47653734	C	T	34	GENIC	heterozygous	119416554
17	47653921	47653922	G	A	29	GENIC	heterozygous	119291088