chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54152039	54152040	C	T	61	GENIC	homozygous	109940897
19	54152043	54152044	C	G	62	GENIC	homozygous	109940899
19	54152175	54152176	A	G	50	GENIC	homozygous	109940901
19	54152259	54152260	T	G	47	GENIC	homozygous	109732910
19	54152497	54152498	C	T	76	GENIC	homozygous	109940903
19	54152704	54152705	T	C	51	GENIC	homozygous	109940906
19	54152736	54152737	C	T	53	GENIC	homozygous	109940908
19	54153079	54153080	G	A	71	GENIC	homozygous	133340406
19	54153807	54153808	C	G	30	GENIC	homozygous	133340407
19	54153849	54153854	AAAAG		36	GENIC	homozygous	133332237
19	54154163	54154164	C	A	65	GENIC	possibly homozygous	109940910
19	54154291	54154292	C	T	51	GENIC	homozygous	109940912
19	54154389	54154390	C	G	57	GENIC	homozygous	109940914
19	54154593	54154594	A	G	71	GENIC	homozygous	109940916
19	54155704	54155705	A	G	47	GENIC	homozygous	109732912
19	54156735	54156736	C	T	64	GENIC	homozygous	109732919
19	54158865	54158866	G	A	61	GENIC	homozygous	109940918
19	54160283	54160284	C	T	55	GENIC	homozygous	109732929
19	54161064	54161079	CCCAAGACAAACAGG		63	GENIC	homozygous	133332238
19	54161193	54161194	G		49	GENIC	homozygous	132765671
19	54161346	54161347	A	G	53	GENIC	homozygous	109940920