chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44231840	44231841	T	C	34	GENIC	homozygous	109710414
19	44232248	44232249	C	T	38	GENIC	homozygous	109784709
19	44233209	44233210	T	C	32	GENIC	homozygous	109784711
19	44233347	44233348	A	T	38	GENIC	homozygous	109784713
19	44233409	44233410	A	C	37	GENIC	homozygous	109784715
19	44233447	44233448	G	A	33	GENIC	homozygous	109784717
19	44233549	44233550	C	T	30	GENIC	homozygous	119665806
19	44232659	44232660	G		31	GENIC	homozygous	131219644
19	44232735	44232736	C	T	30	GENIC	homozygous	119665801
19	44232744	44232745	C	T	30	GENIC	homozygous	119665802
19	44232746	44232747	C	T	30	GENIC	homozygous	119665803
19	44232986	44232987	A	T	32	GENIC	homozygous	119665804
19	44232999	44233000	C	G	30	GENIC	homozygous	119665805
19	44232822	44232823	G	A	30	GENIC	homozygous	119630860
19	44233550	44233551	G	A	30	GENIC	homozygous	119665807
19	44233570	44233571	G	A	39	GENIC	homozygous	119665808
19	44233589	44233590	T	G	43	GENIC	homozygous	119665809
19	44233596	44233597	C	T	44	GENIC	homozygous	119665810
19	44234230	44234231	G	A	34	GENIC	homozygous	109784719
19	44235007	44235008	G	A	43	GENIC	homozygous	109784721
19	44235077	44235078	T	C	36	GENIC	homozygous	109784723
19	44237785	44237786	A	G	46	GENIC	homozygous	109784725
19	44234850	44234851	C	A	38	GENIC	homozygous	109870503