chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	14553150	14553151	G	A	25	GENIC	homozygous	117830991
9	14553261	14553262	T	A	16	GENIC	possibly homozygous	120452308
9	14553752	14553753	C	T	23	GENIC	possibly homozygous	117830993
9	14556284	14556285	T	C	19	GENIC	possibly homozygous	117830995
9	14557459	14557460	C	A	32	GENIC	possibly homozygous	117830997
9	14557867	14557868	C	G	29	GENIC	homozygous	117830999
9	14557899	14557900	A	G	22	GENIC	homozygous	117266207
9	14558993	14558994	G	A	30	GENIC	homozygous	120452309
9	14559015	14559016	A	G	27	GENIC	homozygous	120452310
9	14560498	14560499	G	A	27	GENIC	possibly homozygous	117831003
9	14562303	14562304	G	T	33	GENIC	possibly homozygous	117831011
9	14561041	14561042	A	G	16	GENIC	homozygous	117831005
9	14561157	14561158	T	G	24	GENIC	homozygous	117831007
9	14561739	14561740	G	A	41	GENIC	possibly homozygous	117831009
9	14562874	14562875	T	A	18	GENIC	homozygous	117831012
9	14562903	14562904	A	G	20	GENIC	homozygous	120452311
9	14563606	14563607	C	T	9	GENIC	homozygous	120452312
9	14564320	14564321	C	T	24	GENIC	possibly homozygous	117831014
9	14566139	14566140	T	G	26	GENIC	homozygous	120452313
9	14566141	14566142	T	C	26	GENIC	homozygous	117266219
9	14566142	14566143	T	C	26	GENIC	homozygous	117266220
9	14567226	14567227	G	A	31	GENIC	homozygous	117831016
9	14567341	14567342	G	T	22	GENIC	possibly homozygous	117831018
9	14567567	14567568	T	C	18	GENIC	possibly homozygous	117831020
9	14567888	14567889	G	A	18	GENIC	homozygous	117831022
9	14569449	14569450	G	A	20	GENIC	homozygous	117831024
9	14570900	14570901	G	A	31	GENIC	homozygous	117831026
9	14570951	14570952	T	C	28	GENIC	possibly homozygous	117831028
9	14575103	14575104	C	T	27	GENIC	homozygous	117831030