chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	101631286	101631287	A	T	13	GENIC	possibly homozygous	117621495
9	101631862	101631863	G	A	19	GENIC	homozygous	117621499
9	101631926	101631927	C	A	19	GENIC	homozygous	117621501
9	101632283	101632284	C	G	15	GENIC	homozygous	117621505
9	101632461	101632462	G	A	25	GENIC	homozygous	120296505
9	101632580	101632581	A	G	25	GENIC	homozygous	117621509
9	101633141	101633142	T	C	17	GENIC	homozygous	120296506
9	101635850	101635851	T	A	31	GENIC	homozygous	117621517
9	101635866	101635867	G	A	33	GENIC	homozygous	117621519
9	101636141	101636142	C	T	16	GENIC	homozygous	120296507
9	101637037	101637038	C	T	22	GENIC	homozygous	120296508
9	101637710	101637711	C	T	19	GENIC	homozygous	120296509
9	101639486	101639487	C	T	27	GENIC	homozygous	117621521
9	101641966	101641967	G	T	35	GENIC	homozygous	120296510
9	101641993	101641994	G	A	38	GENIC	homozygous	120296511
9	101642379	101642380	C	T	37	GENIC	homozygous	120296512
9	101643952	101643953	A	G	19	GENIC	homozygous	120296513
9	101645249	101645250	T	C	6	GENIC	homozygous	117621533
9	101646287	101646288	G	A	13	GENIC	homozygous	120296514
9	101646691	101646692	T	C	26	GENIC	homozygous	117621537
9	101647582	101647583	C	T	22	GENIC	homozygous	120296515
9	101648590	101648591	C	T	22	GENIC	homozygous	120296516
9	101649943	101649944	G	T	22	GENIC	homozygous	120296517
9	101650081	101650082	G	A	23	GENIC	possibly homozygous	117732004
9	101651885	101651886	G	C	28	GENIC	homozygous	117621539
9	101653366	101653367	G	T	23	GENIC	homozygous	117621547
9	101667125	101667126	C	G	19	GENIC	homozygous	117621565
9	101668680	101668681	T	A	27	GENIC	homozygous	117621575
9	101668682	101668683	T	A	27	GENIC	homozygous	117621577
9	101669527	101669528	C	G	20	GENIC	homozygous	120296522
9	101670690	101670691	A	C	16	GENIC	homozygous	120296523
9	101670915	101670916	G	T	23	GENIC	homozygous	117621581
9	101671764	101671765	C	T	18	GENIC	homozygous	117607348