chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54152039	54152040	C	T	26	GENIC	homozygous	109940897
19	54152043	54152044	C	G	26	GENIC	homozygous	109940899
19	54152175	54152176	A	G	18	GENIC	homozygous	109940901
19	54152259	54152260	T	G	24	GENIC	homozygous	109732910
19	54152497	54152498	C	T	24	GENIC	homozygous	109940903
19	54152704	54152705	T	C	27	GENIC	homozygous	109940906
19	54152736	54152737	C	T	21	GENIC	homozygous	109940908
19	54154163	54154164	C	A	31	GENIC	homozygous	109940910
19	54154291	54154292	C	T	25	GENIC	homozygous	109940912
19	54154389	54154390	C	G	19	GENIC	homozygous	109940914
19	54154593	54154594	A	G	25	GENIC	homozygous	109940916
19	54155704	54155705	A	G	16	GENIC	homozygous	109732912
19	54156735	54156736	C	T	21	GENIC	homozygous	109732919
19	54158865	54158866	G	A	25	GENIC	homozygous	109940918
19	54160283	54160284	C	T	35	GENIC	homozygous	109732929
19	54161346	54161347	A	G	28	GENIC	homozygous	109940920