chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	31494051	31494052	C	A	27	GENIC	homozygous	108713959
1	31494090	31494091	C	A	20	GENIC	homozygous	108713961
1	31494920	31494921	T	C	37	GENIC	homozygous	108713963
1	31494970	31494971	T	C	33	GENIC	homozygous	108713965
1	31494981	31494982	A	T	39	GENIC	homozygous	108713967
1	31495058	31495059	A	G	34	GENIC	homozygous	108713969
1	31495150	31495151	A	T	35	GENIC	homozygous	108713971
1	31495196	31495197	C	A	44	GENIC	homozygous	108713973
1	31495624	31495625	C	T	23	GENIC	homozygous	108713979
1	31495768	31495769	G	A	19	GENIC	homozygous	108713981
1	31496505	31496506	C	G	42	GENIC	homozygous	108713985
1	31496687	31496688	G	A	25	GENIC	homozygous	108713987
1	31496705	31496706	C	T	22	GENIC	homozygous	108713989
1	31496888	31496889	G	A	27	GENIC	homozygous	108713991
1	31497001	31497002	T	C	32	GENIC	homozygous	108713993
1	31497112	31497113	A	C	26	GENIC	homozygous	108713995
1	31497633	31497634	T	A	21	GENIC	homozygous	108713997
1	31497721	31497722	C	T	32	GENIC	homozygous	108713999
1	31498088	31498089	A	G	36	GENIC	homozygous	108714001
1	31498269	31498270	T	C	25	GENIC	homozygous	108714003
1	31499026	31499027	T	C	23	GENIC	homozygous	108714007
1	31499547	31499548	T	C	36	GENIC	homozygous	109072128
1	31499702	31499703	A	C	32	GENIC	homozygous	108714009
1	31499776	31499777	G	A	33	GENIC	homozygous	108714011
1	31500751	31500752	A	C	25	GENIC	homozygous	109072130
1	31501758	31501759	G	C	3	GENIC	homozygous	120553045
1	31505258	31505259	G	A	23	GENIC	homozygous	108714091
1	31505375	31505376	C	A	31	GENIC	homozygous	108714095
1	31506209	31506210	C	T	39	GENIC	homozygous	109072148
1	31506258	31506259	C	T	34	GENIC	homozygous	109072150
1	31511087	31511088	T	C	28	GENIC	homozygous	108714125
1	31511098	31511099	A	G	26	GENIC	homozygous	108714127
1	31512428	31512429	G	A	25	GENIC	homozygous	108714137
1	31512518	31512519	A	G	30	GENIC	homozygous	108714139
1	31515019	31515020	A	C	31	GENIC	homozygous	109072154
1	31517577	31517578	A	G	44	GENIC	homozygous	108714251