chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	43680583	43680584	T	C	31	GENIC	homozygous	111053499
17	43680897	43680898	A	G	26	GENIC	homozygous	111053501
17	43680999	43681000	C	T	23	GENIC	homozygous	111053503
17	43681261	43681262	G	A	16	GENIC	homozygous	111053506
17	43681262	43681263	A	T	16	GENIC	homozygous	111053508
17	43681649	43681650	C	A	23	GENIC	homozygous	111053512
17	43681656	43681657	G	A	22	GENIC	homozygous	111053514
17	43682451	43682452	C	G	30	GENIC	homozygous	111053516
17	43683383	43683384	T	C	18	GENIC	homozygous	111053518
17	43683980	43683981	C	A	15	GENIC	homozygous	111053520
17	43684368	43684369	T	C	21	GENIC	homozygous	111053522
17	43684386	43684387	C	A	19	GENIC	homozygous	111053524
17	43686692	43686693	T	C	7	GENIC	homozygous	111053526
17	43686736	43686737	T	C	12	GENIC	homozygous	111053528
17	43686847	43686848	A	G	23	GENIC	homozygous	111053530
17	43686935	43686936	T	C	18	GENIC	homozygous	111053532
17	43687771	43687772	G	T	28	GENIC	homozygous	111053534
17	43687817	43687818	A	C	21	GENIC	homozygous	111053536
17	43688737	43688738	C	A	18	GENIC	homozygous	111053538
17	43688749	43688750	G	A	15	GENIC	homozygous	111053540
17	43689225	43689226	G	C	13	GENIC	homozygous	111053542
17	43689231	43689232	A	T	14	GENIC	homozygous	111053544