chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	113579351	113579352	G	C	22	GENIC	heterozygous	120284681
9	113579360	113579361	T	C	22	GENIC	heterozygous	117631171
9	113579659	113579660	C	T	20	GENIC	homozygous	117631173
9	113579830	113579831	G	C	33	GENIC	heterozygous	117427220
9	113580060	113580061	G	A	15	GENIC	homozygous	117631175
9	113580153	113580154	A	T	17	GENIC	heterozygous	117427222
9	113580265	113580266	G	C	22	GENIC	heterozygous	117427225
9	113585514	113585515	G	A	22	GENIC	homozygous	117631183
9	113585908	113585909	T	C	25	GENIC	homozygous	117631185
9	113585964	113585965	C	A	16	GENIC	possibly homozygous	117631187
9	113588660	113588661	A	T	27	GENIC	homozygous	117631189
9	113580313	113580314	C	T	26	GENIC	heterozygous	128779758
9	113580316	113580317	C	G	26	GENIC	heterozygous	128779759
9	113580369	113580369		C	17	GENIC	heterozygous	128746396
9	113581328	113581329	C		24	GENIC	homozygous	128746397
9	113580413	113580414	T	G	20	GENIC	heterozygous	117831324
9	113580430	113580431	A	T	19	GENIC	heterozygous	117831326
9	113588989	113588990	G	T	31	GENIC	homozygous	117631191
9	113588994	113588995	G	C	31	GENIC	homozygous	117631193
9	113591817	113591818	C	T	26	GENIC	homozygous	117645427
9	113592821	113592822	T	C	13	GENIC	homozygous	117427237
9	113594294	113594295	G	A	21	GENIC	homozygous	117631195
9	113594383	113594384	T	C	17	GENIC	homozygous	117645430
9	113596836	113596837	T	C	15	GENIC	homozygous	117645432
9	113594928	113594943	TGCTTTTCTTCTTTG		17	GENIC	homozygous	131456378
9	113597006	113597007	A		13	GENIC	heterozygous	131456379