chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	20576736	20576737	T	C	42	GENIC	homozygous	109132562
20	20577325	20577326	C	T	50	GENIC	homozygous	109556525
20	20578344	20578345	G	A	53	GENIC	homozygous	109556527
20	20580754	20580755	T	C	44	GENIC	possibly homozygous	109556529
20	20580814	20580815	G	A	32	GENIC	homozygous	109556531
20	20581300	20581301	C	G	37	GENIC	possibly homozygous	109132574
20	20582631	20582632	T	C	56	GENIC	homozygous	109132576
20	20582778	20582779	G	A	46	GENIC	homozygous	109556533
20	20584114	20584115	A	G	35	GENIC	heterozygous	119882809
20	20585695	20585696	A	G	44	GENIC	homozygous	109132580
20	20587180	20587181	G	A	40	GENIC	homozygous	109132582
20	20587562	20587563	G	A	42	GENIC	homozygous	109132584
20	20588145	20588146	T	C	24	GENIC	possibly homozygous	119882810
20	20588650	20588651	A	G	53	GENIC	homozygous	109556537
20	20588892	20588893	G	A	45	GENIC	homozygous	109556539
20	20589145	20589146	T	C	35	GENIC	homozygous	109556541
20	20589207	20589208	T	C	52	GENIC	possibly homozygous	109556543
20	20589659	20589660	A	G	54	GENIC	homozygous	109132586
20	20590343	20590344	C	T	65	GENIC	possibly homozygous	109556545
20	20590486	20590487	G	A	61	GENIC	homozygous	109556547
20	20590532	20590533	C	T	59	GENIC	homozygous	109556549
20	20590660	20590661	A	G	50	GENIC	homozygous	109556551