chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	60025208	60025209	T	A	15	GENIC	homozygous	109748587
19	60051950	60051951	G	A	25	GENIC	homozygous	109793462
19	60051951	60051952	A	G	27	GENIC	homozygous	109793464
19	60167896	60167897	A	G	11	GENIC	homozygous	109748988
19	60337530	60337531	C	A	16	GENIC	homozygous	109878791
19	60337617	60337618	G	T	9	GENIC	homozygous	109793486
19	60337859	60337860	A	G	11	GENIC	homozygous	109793488
19	60337861	60337862	G	T	11	GENIC	homozygous	109793490
19	60338002	60338003	C	G	12	GENIC	homozygous	109793492
19	60345296	60345297	C	A	3	GENIC	homozygous	109749743
19	60345297	60345298	A	C	3	GENIC	homozygous	109749745
19	60411947	60411948	A	G	26	GENIC	homozygous	109750061
19	60462583	60462584	A	C	30	GENIC	homozygous	109750259
19	60462623	60462624	G	T	23	GENIC	homozygous	109750261
19	60462679	60462680	T	G	17	GENIC	homozygous	109750263
19	60462680	60462681	G	T	17	GENIC	homozygous	109750265
19	60508230	60508231	C	A	23	GENIC	homozygous	109793502
19	60508240	60508241	C	T	22	GENIC	homozygous	109793504
19	60508242	60508243	C	A	20	GENIC	homozygous	109793506
19	60508245	60508246	C	G	23	GENIC	homozygous	109793508