chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	33132041	33132042	C	T	61	GENIC	heterozygous	118751604
14	33132061	33132062	C	T	68	GENIC	heterozygous	118751605
14	33132522	33132523	C	T	36	GENIC	homozygous	118687416
14	33132771	33132772	T	A	59	GENIC	homozygous	114219065
14	33136852	33136853	A	C	30	GENIC	homozygous	113417800
14	33133357	33133358	G	A	56	GENIC	homozygous	113417797
14	33134584	33134585	A	G	49	GENIC	homozygous	113417798
14	33136848	33136849	C	A	28	GENIC	homozygous	113417799
14	33137044	33137045	T	C	49	GENIC	homozygous	113417801
14	33138888	33138889	C	T	12	GENIC	homozygous	113417802
14	33139278	33139279	C	G	30	GENIC	homozygous	118687418
14	33139296	33139297	C	T	28	GENIC	homozygous	118687419
14	33139387	33139388	A	T	38	GENIC	possibly homozygous	113417803
14	33140623	33140624	T	C	57	GENIC	homozygous	113417804
14	33140963	33140964	A	G	27	GENIC	homozygous	113584881
14	33141807	33141808	G	A	43	GENIC	homozygous	113417805
14	33142792	33142793	T	C	16	GENIC	homozygous	113417806
14	33142942	33142943	A	G	53	GENIC	homozygous	113417807
14	33142957	33142958	T	A	54	GENIC	homozygous	113417808
14	33143145	33143146	A	T	54	GENIC	homozygous	113417809
14	33144686	33144687	T	C	43	GENIC	homozygous	113417810
14	33144753	33144754	A	T	36	GENIC	homozygous	113417811
14	33145107	33145108	G	A	45	GENIC	homozygous	113417812
14	33145691	33145692	C	A	62	GENIC	homozygous	113417813
14	33145762	33145763	C	G	44	GENIC	homozygous	113417814
14	33146070	33146071	A	G	28	GENIC	possibly homozygous	113417815
14	33146395	33146396	T	C	39	GENIC	homozygous	113417816
14	33146952	33146953	A	G	48	GENIC	homozygous	113417817
14	33147005	33147006	T	C	47	GENIC	homozygous	113417818
14	33147179	33147180	G	A	47	GENIC	homozygous	113417819
14	33148299	33148300	T	C	32	GENIC	homozygous	113417820
14	33149742	33149743	C	T	20	GENIC	homozygous	113417821
14	33150144	33150145	A	G	33	GENIC	homozygous	113417822
14	33151614	33151615	G	T	56	GENIC	possibly homozygous	113417823
14	33141972	33141973	G	C	28	GENIC	homozygous	113817960