chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	14315887	14315888	G	A	13	GENIC	homozygous	51762500
9	14316654	14316655	A	G	29	GENIC	homozygous	51762502
9	14316970	14316971	C	T	26	GENIC	homozygous	51762504
9	14317217	14317218	C	T	24	GENIC	homozygous	51762506
9	14317415	14317416	C	T	21	GENIC	homozygous	51762508
9	14319291	14319292	T	G	23	GENIC	homozygous	51762510
9	14319591	14319592	T	C	18	GENIC	homozygous	51762512
9	14319709	14319710	G	T	21	GENIC	homozygous	51762514
9	14320363	14320364	C	T	29	GENIC	homozygous	51762516
9	14320390	14320391	A	C	27	GENIC	homozygous	51762518
9	14321207	14321208	C	T	25	GENIC	homozygous	51762520
9	14321212	14321213	A	G	23	GENIC	homozygous	51762522
9	14321343	14321344	C	CT	17	GENIC	possibly homozygous	51762524
9	14321349	14321350	G	T	20	GENIC	homozygous	51762526
9	14321377	14321378	C	G	19	GENIC	homozygous	51762528
9	14321755	14321756	A	G	23	GENIC	homozygous	51762530
9	14321881	14321882	G	A	17	GENIC	homozygous	51762532
9	14321987	14321988	C	T	18	GENIC	homozygous	51762534
9	14322131	14322132	A	G	23	GENIC	homozygous	51762536
9	14322224	14322225	G	A	25	GENIC	homozygous	51762538
9	14322320	14322321	A	G	24	GENIC	homozygous	51762540
9	14322382	14322383	C	T	21	GENIC	homozygous	51762542
9	14322677	14322678	C	T	23	GENIC	homozygous	51762544
9	14322784	14322785	T	C	31	GENIC	homozygous	51762546
9	14322855	14322856	T	A	29	GENIC	homozygous	51762548
9	14323714	14323715	C	T	13	GENIC	homozygous	51762550
9	14323826	14323827	A	G	21	GENIC	homozygous	51762552
9	14323857	14323858	T	TGCATGGAAG	12	GENIC	homozygous	51762554
9	14323893	14323894	T	C	16	GENIC	homozygous	51762556
9	14324075	14324076	G	A	18	GENIC	homozygous	51762558