chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	9622631	9622632	C	A	56	GENIC	homozygous	109630882
19	9622913	9622914	T	C	50	GENIC	homozygous	109630884
19	9623111	9623112	T	C	40	GENIC	homozygous	109630886
19	9623140	9623141	T	C	41	GENIC	homozygous	109630888
19	9623469	9623470	G	A	43	GENIC	possibly homozygous	109630890
19	9623492	9623493	C	T	40	GENIC	homozygous	109630892
19	9623926	9623927	G	T	11	GENIC	homozygous	109993662
19	9624830	9624831	T	A	42	GENIC	possibly homozygous	109630896
19	9625141	9625142	T	C	60	GENIC	homozygous	109630898
19	9625163	9625164	T	C	56	GENIC	homozygous	109630900
19	9625185	9625186	C	T	46	GENIC	homozygous	109630902
19	9625197	9625198	C	T	45	GENIC	homozygous	109630904
19	9625214	9625215	A	C	44	GENIC	homozygous	109630906
19	9625252	9625253	G	A	31	GENIC	homozygous	109630908
19	9625586	9625587	C	T	44	GENIC	heterozygous	109630910
19	9625698	9625699	C	T	55	GENIC	homozygous	109630912
19	9626252	9626253	T	C	42	GENIC	homozygous	119596142
19	9626587	9626588	G	T	41	GENIC	heterozygous	109630914
19	9626613	9626614	T	A	37	GENIC	homozygous	109630916
19	9626616	9626617	C	G	37	GENIC	homozygous	109630918
19	9626890	9626891	T	C	38	GENIC	homozygous	109630920
19	9627655	9627656	C	T	54	GENIC	homozygous	109630922
19	9627966	9627967	G	A	29	GENIC	homozygous	109630924
19	9629027	9629028	A	G	52	GENIC	homozygous	109630926
19	9629046	9629047	A	G	46	GENIC	possibly homozygous	109630928
19	9629229	9629230	A	T	40	GENIC	homozygous	109630930
19	9629295	9629296	G	A	53	GENIC	homozygous	109630932
19	9629298	9629299	A	G	47	GENIC	homozygous	109630934
19	9630725	9630726	T	C	34	GENIC	possibly homozygous	109630936
19	9632370	9632371	T	C	46	GENIC	homozygous	109630938
19	9636845	9636846	C	T	49	GENIC	possibly homozygous	109630940
19	9628579	9628580	T	C	30	GENIC	homozygous	110107293
19	9628989	9628990	T	C	43	GENIC	homozygous	109850012
19	9634923	9634924	G	T	43	GENIC	possibly homozygous	109764321