chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56002196	56002197	T	G	27	GENIC	homozygous	109737556
19	56003316	56003317	T	C	50	GENIC	homozygous	109737558
19	56003398	56003399	C	T	44	GENIC	homozygous	109737560
19	56003863	56003864	T	C	30	GENIC	homozygous	109789087
19	56003905	56003906	T	C	43	GENIC	homozygous	109789089
19	56005110	56005111	C	T	30	GENIC	homozygous	109737562
19	56005310	56005311	A	G	42	GENIC	homozygous	109737564
19	56006263	56006264	A	G	35	GENIC	homozygous	109737566
19	56006531	56006532	A	T	25	GENIC	homozygous	109737568
19	56006698	56006699	A	G	22	GENIC	homozygous	109737570
19	56007004	56007005	C	T	27	GENIC	homozygous	109737572
19	56007099	56007100	C	T	38	GENIC	homozygous	109737574
19	56007980	56007981	C	T	29	GENIC	homozygous	109737576
19	56008186	56008187	C	T	21	GENIC	homozygous	109737578
19	56008577	56008578	A	G	35	GENIC	heterozygous	119633644
19	56008582	56008583	C	A	35	GENIC	heterozygous	119633645
19	56008600	56008601	G	A	33	GENIC	heterozygous	109737580
19	56009529	56009530	C	G	21	GENIC	homozygous	109737582