chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	31871553	31871554	A	G	38	GENIC	homozygous	140972115
2	31872321	31872322	C	T	39	GENIC	homozygous	142930535
2	31872626	31872627	T	C	34	GENIC	homozygous	142930536
2	31872830	31872831	C	T	25	GENIC	homozygous	142930537
2	31872906	31872907	G	A	27	GENIC	homozygous	142930538
2	31873385	31873386	T		30	GENIC	homozygous	142893248
2	31873645	31873647	AC		30	GENIC	homozygous	142893249
2	31873930	31873931	C	T	41	GENIC	homozygous	142930539
2	31874070	31874070		A	33	GENIC	possibly homozygous	142893250
2	31874351	31874352	G	A	29	GENIC	homozygous	142930540
2	31875540	31875541	C	T	39	GENIC	homozygous	140972117
2	31875739	31875740	A	G	42	GENIC	homozygous	140972118
2	31877481	31877482	G		49	GENIC	homozygous	142893251
2	31873129	31873129		AG	11	GENIC	homozygous	147245635
2	31876343	31876344	T	G	46	GENIC	homozygous	140972119
2	31876884	31876885	A	G	46	GENIC	homozygous	140972120
2	31876992	31876993	G	A	39	GENIC	homozygous	142930541
2	31873152	31873153	G		15	GENIC	homozygous	147245636
2	31875966	31875967	A		34	GENIC	homozygous	140967188
2	31877972	31877973	C	T	42	GENIC	homozygous	142930542
2	31877976	31877977	A	G	42	GENIC	homozygous	142930543
2	31878168	31878169	C	G	38	GENIC	homozygous	140972123
2	31873158	31873159	C		16	GENIC	heterozygous	402996544
2	31873158	31873159	C	G	16	GENIC	homozygous	402996545