chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	63114943	63114944	C	G	23	GENIC	homozygous	111210534
17	63121795	63121796	A	T	17	GENIC	homozygous	111075405
17	63139376	63139377	G	A	24	GENIC	homozygous	111075407
17	63139655	63139656	T	C	29	GENIC	homozygous	111075408
17	63140491	63140492	A	T	19	GENIC	homozygous	111210540
17	63140648	63140649	A	T	23	GENIC	homozygous	111075409
17	63140725	63140726	C	T	22	GENIC	homozygous	111075411
17	63141606	63141607	C	T	14	GENIC	homozygous	111210541
17	63141651	63141652	C	T	23	GENIC	homozygous	111075412
17	63141849	63141850	T	C	32	GENIC	homozygous	111075413
17	63142339	63142340	T	C	15	GENIC	homozygous	111075414
17	63142378	63142379	T	C	12	GENIC	homozygous	111075415
17	63142415	63142416	G	T	18	GENIC	homozygous	111075416
17	63143832	63143833	T	G	24	GENIC	homozygous	111075418
17	63144219	63144220	G	A	21	GENIC	homozygous	111075419
17	63144837	63144838	A	G	25	GENIC	homozygous	111075420
17	63145095	63145096	T	C	28	GENIC	homozygous	111210542
17	63145371	63145372	A	G	12	GENIC	homozygous	111075421