chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54694417	54694418	A	G	10	GENIC	homozygous	109734994
19	54695244	54695245	C	T	7	GENIC	homozygous	109734996
19	54695247	54695248	T	C	5	GENIC	homozygous	109734998
19	54695744	54695745	G	A	23	GENIC	homozygous	109735000
19	54695810	54695811	C	T	25	GENIC	homozygous	109735002
19	54697930	54697931	G	A	9	GENIC	homozygous	109735004
19	54703976	54703977	C	T	18	GENIC	homozygous	109735006
19	54705172	54705173	G	A	21	GENIC	homozygous	109735008
19	54705202	54705203	C	T	21	GENIC	homozygous	109735010
19	54705363	54705364	A	G	13	GENIC	homozygous	109735012
19	54707916	54707917	T	A	14	GENIC	homozygous	109735014
19	54708404	54708405	C	A	9	GENIC	heterozygous	125267106
19	54709748	54709749	C	G	9	GENIC	homozygous	109735016
19	54712157	54712158	A	G	8	GENIC	homozygous	109735020
19	54712215	54712216	G	C	13	GENIC	homozygous	109977718
19	54717346	54717347	T	C	10	GENIC	homozygous	109735024
19	54717484	54717485	A	G	13	GENIC	homozygous	109735026
19	54718478	54718479	T	C	20	GENIC	homozygous	109735028
19	54719683	54719684	G	A	25	GENIC	homozygous	109735030
19	54720574	54720575	G	A	12	GENIC	heterozygous	109735032
19	54721678	54721679	A	C	16	GENIC	homozygous	109735034