chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	236649685	236649686	A	G	8	GENIC	homozygous	109012465
1	236649982	236649983	T	C	17	GENIC	homozygous	108574005
1	236650105	236650106	G	A	36	GENIC	homozygous	109204332
1	236650469	236650470	C	T	39	GENIC	homozygous	109204334
1	236651707	236651708	G	T	28	GENIC	homozygous	109204336
1	236651820	236651821	A	G	29	GENIC	homozygous	109204338
1	236652004	236652005	A	G	30	GENIC	homozygous	109204340
1	236652137	236652138	G	T	26	GENIC	homozygous	109204342
1	236652858	236652859	G	A	26	GENIC	homozygous	109204344
1	236652984	236652985	G	A	10	GENIC	homozygous	109204346
1	236653572	236653573	T	G	23	GENIC	homozygous	109204348
1	236655897	236655898	G	A	23	GENIC	homozygous	109204352
1	236656021	236656022	A	G	24	GENIC	homozygous	109204354
1	236656239	236656240	T	C	16	GENIC	homozygous	108574009
1	236656817	236656818	C	T	21	GENIC	homozygous	108574015
1	236656914	236656915	G	A	15	GENIC	homozygous	108574017
1	236657314	236657315	C	T	27	GENIC	homozygous	108574019
1	236657548	236657549	C	T	30	GENIC	homozygous	109204356
1	236657587	236657588	T	C	28	GENIC	homozygous	108574021
1	236657656	236657657	T	C	31	GENIC	homozygous	108574023
1	236658292	236658293	A	T	20	GENIC	homozygous	108574035
1	236659000	236659001	C	A	23	GENIC	homozygous	108574037
1	236659074	236659075	A	G	21	GENIC	homozygous	108574041
1	236659164	236659165	A	G	29	GENIC	homozygous	108574043
1	236659264	236659265	A	G	20	GENIC	homozygous	108574045
1	236659494	236659495	C	T	29	GENIC	homozygous	108574047