chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	26198004	26198005	G	A	34	GENIC	homozygous	109673697
19	26198489	26198490	C	T	25	GENIC	homozygous	109673699
19	26200673	26200674	G	A	35	GENIC	homozygous	109673701
19	26200982	26200983	A	C	33	GENIC	homozygous	109673703
19	26201497	26201498	G	A	21	GENIC	heterozygous	110035694
19	26202559	26202560	A	G	31	GENIC	homozygous	109673705
19	26202625	26202626	C	T	30	GENIC	homozygous	109673707
19	26202753	26202754	T	C	33	GENIC	possibly homozygous	119602598
19	26206253	26206254	A	G	37	GENIC	homozygous	109673709
19	26208476	26208477	G	T	36	GENIC	homozygous	109673711
19	26210812	26210813	C	G	21	GENIC	homozygous	109673713
19	26212538	26212539	T	C	28	GENIC	homozygous	109867734
19	26213578	26213579	C	T	31	GENIC	homozygous	109673717
19	26213713	26213714	T	C	24	GENIC	homozygous	109673719
19	26215329	26215330	T	C	40	GENIC	homozygous	109673721
19	26212428	26212429	G	A	30	GENIC	possibly homozygous	110064401
19	26210911	26210912	A	G	22	GENIC	heterozygous	109986744