chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52086537	52086538	A	C	56	GENIC	homozygous	109939214
19	52086684	52086685	T	C	49	GENIC	homozygous	109824180
19	52087060	52087061	A	G	38	GENIC	homozygous	109939216
19	52087212	52087213	A	G	41	GENIC	homozygous	109824182
19	52087318	52087319	A	G	43	GENIC	homozygous	109824184
19	52087413	52087414	A	G	39	GENIC	homozygous	109824186
19	52087769	52087770	C	T	62	GENIC	homozygous	109824188
19	52088750	52088751	A	T	66	GENIC	homozygous	109824190
19	52091619	52091620	G	C	64	GENIC	homozygous	109824194
19	52092146	52092147	T	C	50	GENIC	homozygous	109824196
19	52093590	52093591	C	T	53	GENIC	homozygous	109824198
19	52094940	52094941	T	G	69	GENIC	possibly homozygous	109939234
19	52095024	52095025	T	C	57	GENIC	homozygous	109939236
19	52095720	52095721	A	G	51	GENIC	homozygous	109824200
19	52096247	52096248	G	A	39	GENIC	homozygous	109824202
19	52097161	52097162	A	G	42	GENIC	homozygous	109824204
19	52097763	52097764	G	A	57	GENIC	homozygous	109824206
19	52098256	52098257	A	T	18	GENIC	homozygous	109939250
19	52099366	52099367	A	G	44	GENIC	homozygous	109824208
19	52100429	52100430	A	G	12	GENIC	homozygous	109939260
19	52102176	52102177	C	T	41	GENIC	homozygous	109824210
19	52103199	52103200	A	G	69	GENIC	possibly homozygous	109824212
19	52103466	52103467	G	A	75	GENIC	homozygous	109824214
19	52104884	52104885	C	T	55	GENIC	homozygous	109824216
19	52105838	52105839	C	T	59	GENIC	homozygous	109824218
19	52106652	52106653	C	T	49	GENIC	homozygous	109824222
19	52108499	52108500	T	C	48	GENIC	homozygous	109824224
19	52109205	52109206	C	A	70	GENIC	homozygous	109824226
19	52110205	52110206	A	G	36	GENIC	homozygous	109824228
19	52112328	52112329	G	A	48	GENIC	homozygous	109824230
19	52112539	52112540	G	A	42	GENIC	homozygous	109824232