chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	118835618	118835619	C	T	39	GENIC	possibly homozygous	116342371
7	118835661	118835662	G	A	41	GENIC	possibly homozygous	116342373
7	118835905	118835906	T	C	25	GENIC	possibly homozygous	116342375
7	118836196	118836197	T	C	28	GENIC	homozygous	115850141
7	118836248	118836249	C	T	33	GENIC	possibly homozygous	116342379
7	118836250	118836251	C	T	33	GENIC	possibly homozygous	116342381
7	118836338	118836339	T	C	30	GENIC	homozygous	115850143
7	118836408	118836409	G	T	24	GENIC	possibly homozygous	116342383
7	118836442	118836443	T	C	18	GENIC	homozygous	116342385
7	118836466	118836467	T	C	19	GENIC	homozygous	116342387
7	118836472	118836473	T	C	14	GENIC	homozygous	116342389
7	118837431	118837432	G	A	36	GENIC	possibly homozygous	116342391
7	118837816	118837817	T	C	35	GENIC	homozygous	116342401
7	118837855	118837856	G	C	26	GENIC	homozygous	116342403
7	118838017	118838018	A	C	21	GENIC	homozygous	116342405
7	118838775	118838776	G	C	26	GENIC	homozygous	115850147
7	118840763	118840764	C	T	30	GENIC	homozygous	116342407
7	118842412	118842413	T	C	32	GENIC	possibly homozygous	115850173
7	118843048	118843049	C	A	31	GENIC	possibly homozygous	115850181
7	118843063	118843064	G	A	33	GENIC	possibly homozygous	116342411
7	118843101	118843102	T	C	24	GENIC	possibly homozygous	115850183
7	118845336	118845337	C	G	25	GENIC	homozygous	116302413
7	118845337	118845338	T	C	24	GENIC	homozygous	118258969
7	118846696	118846697	T	A	31	GENIC	homozygous	115850199
7	118847900	118847901	G	T	28	GENIC	homozygous	116342413
7	118857793	118857794	C	A	56	GENIC	heterozygous	118405508
7	118857794	118857795	A	G	56	GENIC	heterozygous	115850341
7	118857901	118857902	C	T	56	GENIC	heterozygous	116080831
7	118858284	118858285	A	G	54	GENIC	heterozygous	115850353
7	118858296	118858297	G	T	52	GENIC	heterozygous	115850355