chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56276534	56276535	C	G	33	GENIC	homozygous	109738316
19	56277482	56277483	G	A	35	GENIC	homozygous	109738318
19	56279070	56279071	C	T	29	GENIC	homozygous	109738320
19	56281424	56281425	A	G	29	GENIC	homozygous	109738322
19	56281487	56281488	T	C	30	GENIC	homozygous	109738324
19	56282979	56282980	G	A	30	GENIC	homozygous	109738326
19	56284071	56284072	T	G	36	GENIC	homozygous	109738328
19	56288164	56288165	C	G	29	GENIC	homozygous	109738332
19	56288200	56288201	G	A	29	GENIC	homozygous	109738334
19	56288256	56288257	G	A	35	GENIC	homozygous	109738336
19	56288514	56288515	T	C	35	GENIC	homozygous	109789132
19	56291411	56291412	C	G	35	GENIC	homozygous	109738338
19	56291747	56291748	G	T	30	GENIC	homozygous	109738340
19	56292332	56292333	A	G	32	GENIC	homozygous	109738342
19	56293998	56293999	G	A	36	GENIC	homozygous	109738346
19	56294123	56294124	C	T	25	GENIC	homozygous	109738348
19	56294792	56294793	T	C	33	GENIC	homozygous	109738350
19	56294833	56294834	G	A	26	GENIC	homozygous	109738352
19	56295000	56295001	C	T	32	GENIC	homozygous	109738354
19	56295330	56295331	A	G	26	GENIC	homozygous	109738356
19	56295333	56295334	T	C	27	GENIC	homozygous	109738358
19	56296688	56296689	C	T	38	GENIC	homozygous	109738360