chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44231840	44231841	T	C	18	GENIC	homozygous	109710414
19	44232407	44232408	G	A	13	GENIC	homozygous	109929351
19	44232659	44232660	G		8	GENIC	homozygous	131219644
19	44233209	44233210	T	C	18	GENIC	homozygous	109784711
19	44233347	44233348	A	T	14	GENIC	homozygous	109784713
19	44233447	44233448	G	A	15	GENIC	homozygous	109784717
19	44233570	44233571	G	A	15	GENIC	homozygous	119665808
19	44233589	44233590	T	G	15	GENIC	homozygous	119665809
19	44233596	44233597	C	T	14	GENIC	homozygous	119665810
19	44234164	44234165	C	T	14	GENIC	homozygous	109929353
19	44234230	44234231	G	A	15	GENIC	homozygous	109784719
19	44235077	44235078	T	C	20	GENIC	homozygous	109784723
19	44235286	44235287	T	G	11	GENIC	homozygous	109929355
19	44235518	44235519	G	A	15	GENIC	homozygous	109929357
19	44237785	44237786	A	G	19	GENIC	homozygous	109784725
19	44233351	44233351		G	14	GENIC	homozygous	131550503
19	44232595	44232596	C	T	15	GENIC	possibly homozygous	131553313
19	44232636	44232637	T	C	8	GENIC	homozygous	131553314
19	44232715	44232716	G	A	9	GENIC	homozygous	131553315
19	44232768	44232769	G	A	7	GENIC	homozygous	131553316
19	44233315	44233316	A		11	GENIC	homozygous	131550502