chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54152724	54152725	G	A	34	GENIC	homozygous	109875753
19	54154292	54154293	G	A	35	GENIC	homozygous	109875755
19	54154293	54154294	A	T	36	GENIC	homozygous	109890229
19	54154539	54154540	C	T	32	GENIC	possibly homozygous	109875757
19	54155704	54155705	A	G	31	GENIC	homozygous	109732912
19	54155920	54155921	G	A	51	GENIC	homozygous	109875759
19	54156044	54156045	T	C	50	GENIC	homozygous	109732914
19	54156067	54156068	G	A	46	GENIC	homozygous	109875761
19	54156070	54156071	G	A	45	GENIC	homozygous	109875763
19	54156735	54156736	C	T	38	GENIC	homozygous	109732919
19	54157108	54157109	T	G	30	GENIC	homozygous	109875765
19	54157344	54157345	A	G	29	GENIC	homozygous	119633212
19	54157668	54157669	T	C	40	GENIC	homozygous	109875767
19	54158331	54158332	C	T	43	GENIC	homozygous	109875769
19	54158418	54158419	A	G	48	GENIC	homozygous	109732923
19	54158554	54158555	T	C	44	GENIC	homozygous	109875771
19	54158802	54158803	G	A	37	GENIC	homozygous	109875773
19	54158864	54158865	C	T	40	GENIC	homozygous	109875775
19	54159402	54159403	G	A	33	GENIC	homozygous	109875777
19	54160283	54160284	C	T	43	GENIC	homozygous	109732929
19	54160987	54160988	T	C	34	GENIC	homozygous	109875779
19	54161209	54161210	C	T	45	GENIC	homozygous	109875781
19	54161493	54161494	T	C	38	GENIC	homozygous	109875783
19	54162469	54162470	G	A	32	GENIC	homozygous	109875785
19	54161193	54161194	G		42	GENIC	homozygous	132765671