chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	38157286	38157287	T	G	26	GENIC	homozygous	113426634
14	38157451	38157452	T	C	21	GENIC	homozygous	113426635
14	38159149	38159150	G	T	21	GENIC	homozygous	113426636
14	38160144	38160145	C	T	20	GENIC	homozygous	113426637
14	38161508	38161509	T	C	20	GENIC	homozygous	113426638
14	38161540	38161541	C	A	16	GENIC	homozygous	113426639
14	38161563	38161564	A	G	13	GENIC	homozygous	113426640
14	38161566	38161567	A	G	12	GENIC	homozygous	113426641
14	38161623	38161624	A	G	20	GENIC	homozygous	113426642
14	38162648	38162649	T	C	16	GENIC	homozygous	113426643
14	38162815	38162816	T	A	17	GENIC	homozygous	113426644
14	38163159	38163160	T	C	14	GENIC	homozygous	118688911
14	38163311	38163312	T	C	29	GENIC	homozygous	113674559
14	38163560	38163561	G	A	16	GENIC	homozygous	113426645
14	38165047	38165048	C	T	27	GENIC	homozygous	113426647
14	38165390	38165391	C	T	23	GENIC	homozygous	113426648
14	38166012	38166013	C	T	18	GENIC	homozygous	113426649
14	38166032	38166033	A	G	21	GENIC	homozygous	113426650
14	38166366	38166367	G	A	12	GENIC	homozygous	113426651
14	38166999	38167000	T	G	11	GENIC	homozygous	113426652
14	38167186	38167187	A	G	25	GENIC	possibly homozygous	118688912
14	38167733	38167734	G	A	17	GENIC	homozygous	113426653
14	38168118	38168119	T	C	14	GENIC	homozygous	113426654
14	38168295	38168296	A	C	20	GENIC	possibly homozygous	113426655
14	38168306	38168307	G	A	19	GENIC	homozygous	113426656
14	38168452	38168453	C	G	22	GENIC	homozygous	113586972
14	38168837	38168838	A	T	11	GENIC	homozygous	118688913
14	38169413	38169414	G	A	21	GENIC	homozygous	113426657
14	38169435	38169436	C	T	15	GENIC	homozygous	113426658
14	38169571	38169572	G	A	26	GENIC	homozygous	113426659
14	38170998	38170999	G	T	17	GENIC	homozygous	113426660
14	38171022	38171023	C	G	16	GENIC	homozygous	113426661