chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25262244	25262245	T	C	53	GENIC	homozygous	109866998
19	25262803	25262803		C	31	GENIC	possibly homozygous	131217358
19	25264273	25264273		C	57	GENIC	homozygous	129595832
19	25264430	25264430		GATGCAGGT	44	GENIC	homozygous	129595833
19	25264596	25264597	C	T	49	GENIC	homozygous	109867000
19	25264806	25264806		A	42	GENIC	possibly homozygous	131217359
19	25265483	25265484	T	C	47	GENIC	homozygous	109867002
19	25265646	25265647	C	A	18	GENIC	homozygous	119678168
19	25266647	25266647		CCTTCTCAAAA	47	GENIC	homozygous	129595834
19	25266880	25266883	CCC		46	GENIC	homozygous	129595835
19	25268408	25268408		TTG	47	GENIC	homozygous	129595836
19	25268449	25268450	C	T	51	GENIC	homozygous	119658118
19	25273541	25273542	C	A	37	GENIC	homozygous	109867008
19	25277655	25277661	AGCACT		50	GENIC	possibly homozygous	131217360
19	25277663	25277664	C	T	50	GENIC	possibly homozygous	109867010
19	25277666	25277667	C	A	49	GENIC	possibly homozygous	109867012
19	25278527	25278528	C	T	39	GENIC	homozygous	124557985
19	25279698	25279699	A	C	46	GENIC	homozygous	109672402
19	25280051	25280052	T	A	50	GENIC	homozygous	124557987
19	25280745	25280745		AC	54	GENIC	homozygous	129595839
19	25281884	25281885	G	A	46	GENIC	homozygous	109867014
19	25282328	25282329	T	C	36	GENIC	homozygous	109867016
19	25282609	25282609		G	39	GENIC	homozygous	131217361
19	25277684	25277685	A		40	GENIC	heterozygous	130799370