chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37481962	37481963	A	G	28	GENIC	homozygous	109693835
19	37484308	37484309	G	A	23	GENIC	homozygous	109693837
19	37486272	37486273	C	T	16	GENIC	homozygous	109693839
19	37488291	37488292	A	G	26	GENIC	homozygous	109693841
19	37490467	37490468	C	T	19	GENIC	homozygous	109693843
19	37491328	37491329	G	A	22	GENIC	homozygous	109693845
19	37494565	37494566	A	G	28	GENIC	homozygous	109693847
19	37494872	37494873	G	A	30	GENIC	homozygous	109693849
19	37497103	37497104	A	C	24	GENIC	homozygous	109693851
19	37500283	37500284	T	G	21	GENIC	homozygous	109693853
19	37500388	37500389	C	T	12	GENIC	homozygous	109693855
19	37500699	37500700	T	C	17	GENIC	homozygous	109693858
19	37502308	37502309	G	A	19	GENIC	homozygous	109693860
19	37507041	37507042	C	T	29	GENIC	homozygous	109693862
19	37508064	37508065	C	T	32	GENIC	homozygous	109693864
19	37518386	37518387	G	A	14	GENIC	homozygous	109693866
19	37522031	37522032	G	A	26	GENIC	homozygous	109693868
19	37524278	37524279	T	C	10	GENIC	homozygous	109693870