chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	18594615	18594616	A	G	45	GENIC	possibly homozygous	109123488
20	18595396	18595397	A	G	56	GENIC	possibly homozygous	119775303
20	18599176	18599177	G	A	70	GENIC	homozygous	109123489
20	18599425	18599426	C	T	71	GENIC	possibly homozygous	109123490
20	18599729	18599730	T	A	68	GENIC	homozygous	109123491
20	18599748	18599749	T	A	63	GENIC	homozygous	109123492
20	18600778	18600779	C	T	52	GENIC	possibly homozygous	119775305
20	18601174	18601175	A	G	50	GENIC	possibly homozygous	119775307
20	18601753	18601754	G	A	50	GENIC	possibly homozygous	119775309
20	18601900	18601901	T	A	39	GENIC	possibly homozygous	119775311
20	18602335	18602336	C	T	40	GENIC	homozygous	109123493
20	18602865	18602866	C	T	82	GENIC	possibly homozygous	109123494
20	18602965	18602966	A	G	74	GENIC	possibly homozygous	109123495
20	18603261	18603262	G	A	61	GENIC	homozygous	109123496
20	18604024	18604025	T	C	61	GENIC	homozygous	109123497
20	18604770	18604771	C	T	74	GENIC	possibly homozygous	109123499
20	18605755	18605756	T	C	90	GENIC	possibly homozygous	109123501
20	18605911	18605912	G	A	49	GENIC	homozygous	109123503
20	18605934	18605935	T	C	53	GENIC	homozygous	109123505