chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44231840	44231841	T	C	52	GENIC	homozygous	109710414
19	44232248	44232249	C	T	33	GENIC	homozygous	109784709
19	44232314	44232315	G	A	39	GENIC	homozygous	109818711
19	44233209	44233210	T	C	37	GENIC	homozygous	109784711
19	44232659	44232660	G		29	GENIC	homozygous	131219644
19	44232735	44232736	C	T	39	GENIC	homozygous	119665801
19	44232744	44232745	C	T	36	GENIC	homozygous	119665802
19	44232746	44232747	C	T	37	GENIC	homozygous	119665803
19	44232986	44232987	A	T	52	GENIC	homozygous	119665804
19	44232822	44232823	G	A	32	GENIC	homozygous	119630860
19	44233357	44233358	A	G	46	GENIC	homozygous	109818713
19	44233589	44233590	T	G	53	GENIC	homozygous	119665809
19	44234093	44234094	A	G	49	GENIC	homozygous	109818715
19	44234549	44234550	T	C	57	GENIC	homozygous	109818717
19	44234766	44234767	A	G	46	GENIC	homozygous	109818719
19	44235077	44235078	T	C	52	GENIC	homozygous	109784723
19	44235908	44235909	T	A	41	GENIC	homozygous	109818721
19	44236505	44236506	C	A	46	GENIC	homozygous	109818723
19	44237785	44237786	A	G	47	GENIC	homozygous	109784725