chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	109075741	109075742	T	A	18	GENIC	homozygous	108174236
1	109078281	109078282	T	G	21	GENIC	homozygous	108174239
1	109079589	109079590	T	G	26	GENIC	homozygous	108174241
1	109080239	109080240	T	A	19	GENIC	homozygous	108174242
1	109082572	109082573	C	A	15	GENIC	homozygous	108174243
1	109084373	109084374	G	A	9	GENIC	homozygous	108174244
1	109085756	109085757	C	T	15	GENIC	homozygous	108174246
1	109085826	109085827	G	C	18	GENIC	homozygous	108174247
1	109085833	109085834	C	T	20	GENIC	homozygous	108174248
1	109086121	109086122	T	C	13	GENIC	homozygous	108174249
1	109086562	109086563	T	A	12	GENIC	homozygous	108174250
1	109086825	109086826	T	C	14	GENIC	homozygous	108174251
1	109087445	109087446	G	T	13	GENIC	homozygous	108174253
1	109087540	109087541	T	C	28	GENIC	homozygous	108174254
1	109087773	109087774	G	A	16	GENIC	homozygous	108174255
1	109087957	109087958	T	C	32	GENIC	homozygous	108174256
1	109088046	109088047	G	C	19	GENIC	homozygous	108174257
1	109088097	109088098	G	C	21	GENIC	homozygous	108174258
1	109088167	109088168	G	T	21	GENIC	homozygous	108174259
1	109088259	109088260	C	T	30	GENIC	homozygous	108174260
1	109088827	109088828	A	T	33	GENIC	homozygous	108174264
1	109089113	109089114	C	T	27	GENIC	homozygous	108174265
1	109089217	109089218	T	C	33	GENIC	homozygous	108174266
1	109090101	109090102	T	C	13	GENIC	homozygous	120669355
1	109090103	109090104	T	C	12	GENIC	homozygous	108174274
1	109090109	109090110	T	C	13	GENIC	homozygous	108174275
1	109090180	109090181	G	T	24	GENIC	homozygous	108174276
1	109090223	109090224	C	T	29	GENIC	homozygous	108174277
1	109090268	109090269	T	C	40	GENIC	homozygous	108174278
1	109090411	109090412	G	C	37	GENIC	homozygous	108174279
1	109091619	109091620	A	T	20	GENIC	homozygous	108174281
1	109091803	109091804	A	C	32	GENIC	possibly homozygous	108174282
1	109092474	109092475	C	T	31	GENIC	homozygous	108174283
1	109092737	109092738	A	G	25	GENIC	homozygous	108174284