iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

NCF2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs545730713	snp	G/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183568955	CATTCCTTTCTAGCC[G/T]GACATTCTAGAAGAC	4688
rs545769304	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565833	AAAGTTCCCAGGCAG[A/G]GGTGGATGTGGGGAA	4688
rs545886236	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564942	GGCTCGGGGGAGAAA[A/G]ATAGAATGGAGCAGG	4688
rs545984071	snp	C/G/T	9.88361e-05	0.00702917	missense	NCF2	GRCh38.p7	1:183586977	TGCTTCTGGTAAAGG[C/G/T]CTGAGGAGAGAAGGG	4688
rs545993429	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559794	AACCCAGGAGGGGGA[A/G]GTTGCAGTGAGCCGA	4688
rs546020853	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183586548	GCAGTTTCATGATCA[A/T]CCCCATTCTGTGACA	4688
rs546047247	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183580089	TAAGGAACGGGTGCC[A/T]GTGTGGCTGGGGGAG	4688
rs546292292	in-del	-/AGAC			intron-variant	NCF2	GRCh38.p7	1:183556356	TGATCAACAGGGAAA[-/AGAC]AGACAGTATTGCAAA	4688
rs546313629	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576618	TGAGAAACCTTACTC[A/G]AGAAGTTGGTCGAAT	4688
rs546373985	snp	A/G	6.595e-05	0.00574201	synonymous-codon	NCF2	GRCh38.p7	1:183563538	GACTACCGTGTACTT[A/G]TAGTGCACCTTGAGT	4688
rs546463172	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576767	AGACTCTATTATTAG[C/T]CCTGAGCGACCCTGG	4688
rs546529394	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183581859	TTTTTAGTAGAGCCA[C/G]GGTTTCACCGTGTTA	4688
rs546593253	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183582243	TCAGCGGTTCTCTTC[A/G]TGGCCATTTGGAAGC	4688
rs546630092	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183564733	AGCCTCTAGACAAAA[G/T]ATAACAACAAAAAAC	4688
rs547007844	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557600	CGCTAAATTCTGTTT[C/T]CTGTTGAAGTGCTAC	4688
rs547058783	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588824	TGAAGGCCTGGGAGC[A/T]GAGAAGTGAGTGGTG	4688
rs547160947	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562014	TGCCTCAGCCTCCCA[A/C]AGTGTTGGAATTACA	4688
rs547183789	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183582497	ATTTCTGTAATACTC[C/T]TGGGAGGTTTCTTAG	4688
rs547285774	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583771	GCACGGAGGATGCAT[A/G]AGTGGGTGGCAGCAG	4688
rs547318889	in-del	-/GATT	0.00438332	0.0466095	downstream-variant-500B	NCF2	GRCh38.p7	1:183555409	CACTTAAATGTTGGC[-/GATT]GATTGATATATATTC	4688
rs547354656	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568409	TGATCTCAAGTGATC[C/T]GCCCACCTCAGTCTC	4688
rs547494066	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575298	AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT	4688
rs547567404	snp	A/C	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183566860	CACTGCTTTTCTCCC[A/C]TCCAGGGAGAGATCC	4688
rs547632027	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575932	ATTTCTGAGATTCAA[C/T]GAGCTACTGCCTTCT	4688
rs547801762	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183579611	GGGCATGGTGGTGGG[C/T]GCCTGTAGTCCCAGC	4688
rs547848140	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587127	ACCCTGTGCTCTCAC[A/G]GTGCACCCCACTTCG	4688
rs548144373	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183574294	GATGCCAGGGCTCTG[C/T]CATCCCATACTCTAG	4688
rs548189123	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564340	CAATTAAGCCCACGG[C/G]ATCCAAAGCAATGAA	4688
rs548229821	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571836	GATATTTCCTATAAA[C/T]GGAATTGTACAACAT	4688
rs548229875	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563780	GCTTGGACAGGAATT[C/T]CTACTGAGTAAGATC	4688
rs548251366	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591776	TTACAGGAGTGAGCC[A/G]CCGTGCCCAGCCGAA	4688
rs548350622	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565117	ATGATCAGGCGCGTG[C/T]GGCAATCATTGATCT	4688
rs548359374	snp	C/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591350	AGTCTTGAATGAATT[C/G]CTTGCTCACTTTTTT	4688
rs548372314	snp	A/C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586060	TAACATCTGGCTGGG[A/C/T]GTGGTGGCACATGCC	4688
rs548450805	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592576	TACATTCTAAAAGAA[A/G]TTAGAAATCATTGGT	4688
rs548560095	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578547	TTTTTTATATTTTAA[A/G]TAGAGACCAGGTTTC	4688
rs548750348	snp	C/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183562400	ACACTCACACTCACT[C/G]TTACCCCCAGGATCC	4688
rs548758759	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569995	CCTGGGCTGCATTCC[C/T]CTCATGGCCTCTGGC	4688
rs548820898	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563156	TTGAGGAAGTGGCTC[A/G]GTGGAAATGTAACTT	4688
rs548856506	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183571110	TTGTATAACATCAAA[G/T]TATCTTTTTTTTTTT	4688
rs548914467	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580301	TCATGTCTTTTCCAC[A/G]CATCTTTCTGGGTTC	4688
rs548961014	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183583677	AGCAAATATCTGTCA[C/T]GGGCCAGACATATTA	4688
rs549033920	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590390	GAGAAGACAGGTTGG[A/G]GCGTCTCCCCTAGCA	4688
rs549034602	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183576746	CCAGGGGCCGAGGGC[A/G]GCTACAGACTCTATT	4688
rs549165359	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560379	AACCTGGGATATAAA[C/T]TCATAAAGTTTGTGA	4688
rs549428558	snp	C/G/T	6.59156e-05	0.00574056	missense	NCF2	GRCh38.p7	1:183566957	ATCCGCAGCTCAACT[C/G/T]GTTCAAGGTAGTTGC	4688
rs549528752	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558355	TCACTGCAACCTCCT[C/T]CTCCTGGGTTCAAGA	4688
rs549537701	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183588764	CAGAAGGAATGAGAA[A/G]GCTAGAAGCAGAGGA	4688
rs549670383	snp	A/C	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183589854	AGTTCTGTGTAGAAG[A/C]AAGTACGACTAGGAC	4688
rs549749898	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587828	ATTCAGAATAGATAA[C/T]TTAGACATTTACCTG	4688
rs549821923	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587283	TTAGTCATATATGGC[C/T]TAGAAAAGCTACACA	4688
rs549954173	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573404	ATAACCACATAGAAG[A/C]CCTTTTCCAAATGAG	4688
rs549993576	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183568168	TTGGTACTTTTGTCA[A/C]TTTTTTTTTTTTGAG	4688
rs550009636	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183586569	TTCTGTGACAGCTCA[G/T]TACCTCATAGGAGAC	4688
rs550016991	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566010	AAAGAAGAATCCTAA[C/G]CCGCTAAAACGCCCT	4688
rs550067203	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574696	AAAGGCTCACACGTA[C/T]ACTCTGAGAATGTTG	4688
rs550280245	in-del	-/TGTC			intron-variant	NCF2	GRCh38.p7	1:183558898	ATTTCCCCCTCTCTT[-/TGTC]TGTTGGATTTTCTGT	4688
rs550588578	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183570951	GAGCCTGGTTTCAGA[C/T]GTGGACAGTAACTAA	4688
rs550603270	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563660	GGATCACCGCAGTTT[C/T]GTGATTTGGCACAGG	4688
rs550655767	in-del	-/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183569598	TTAATTTAAAAAAAA[-/T]TTTTTTTTGAGATGG	4688
rs550692398	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585689	GAACTGATGCACACT[A/G]GTGGAACAGTTTCTA	4688
rs550768994	in-del	-/CCT	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183557401	TCTTGATTCTTCTTA[-/CCT]CAGGGTAGGTCGTGG	4688
rs550773018	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590516	TGCATCAGGAAATGT[C/T]CCCACCTTTTGGCAA	4688
rs550827821	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592501	GGCTCCTTGGAAGTT[A/G]GGACCATGCCTTTTC	4688
rs550859182	snp	A/C/G	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555229	GTAACCTAGCTGTGT[A/C/G]GTAGGCTATACCATC	4688
rs551128813	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589036	GAGGTGGGGCCATGT[C/T]CTTCCTCCAGCCAGA	4688
rs551149903	snp	C/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183576522	CAAAGTTCCCACGAT[C/G]CGCAGGACGCACCAC	4688
rs551245144	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183557403	CTTGATTCTTCTTAC[A/C]GGGTAGGTCGTGGAC	4688
rs551263362	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577500	AAAATGGCTTTTCCA[A/G]GCTCCTGGAGGTGTC	4688
rs551339303	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561266	TATGTACCGAGCATT[A/G]TAAGTTCTAGCTTCT	4688
rs551560475	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588270	CTATTTATTGCTCTG[G/T]GGAAGATAAAAAAGA	4688
rs551698492	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183559503	GTGATTCCAGCCCAA[C/T]TTGTTACCTCTGGGA	4688
rs551846553	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581707	AGAGTCTCGCTCTGT[C/T]GCCCTGGCTGGAGTG	4688
rs551909408	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565209	GTGCACTTCCCAAGA[C/T]AGCCCTCTCCACACT	4688
rs551965329	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567797	AGAAACCACCTAGAA[C/T]CAGTGTTGGGCCAGG	4688
rs552084204	snp	A/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183558706	AGCAGCTGGGACTAC[A/T]GATGTGCATCACCAC	4688
rs552220613	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183586185	ACTAAAAATACAAAA[C/T]TAGCTGGGTGTGGTG	4688
rs552295617	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584162	GGCCTTGCCCAGGAA[C/T]GGATCCTCAAGGTTC	4688
rs552349555	snp	C/T	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183579492	AGCACTTTGGGAGAC[C/T]GAGGCGGGTGGATCA	4688
rs552350205	snp	A/T	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183558248	ATTAACTTTTTTTTT[A/T]ATTTTAATTTTTTTG	4688
rs552467709	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580505	CCTGTTTGGGAGCTC[A/G]CTGAAGGTCTCAGAG	4688
rs552531966	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560964	AAATGCAGACTTTCA[A/G]CTCCATCCCAAAACT	4688
rs552548327	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561607	TAGATGCTTAATAAA[A/T]GTTAGTTCATTTTAT	4688
rs552554098	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572704	GAGTACAGTGGTGCA[A/G]TCATAGCTCACTGTA	4688
rs552582135	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591797	CCCAGCCGAAATAAC[C/T]TTTATGAACATTCAT	4688
rs552612155	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562523	TAAACAGCTTTATAC[A/G]CTGCCCTTTTCTAGG	4688
rs552643186	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575138	CCTGTACCAGCACCA[A/G]CAGAACCTGGCCCAG	4688
rs552692396	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569350	AGGGCACAGTCACCC[C/T]GACTAAACACTGGGA	4688
rs552764890	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576495	GTAGCATCTAAAAGC[C/T]AGAGATGCCGTCAAA	4688
rs552828412	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183584183	CTCAAGGTTCACATA[C/T]GGACTTCATATCTAT	4688
rs552974280	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591160	CTCCCCACCCAGGCC[A/G]AGTGGGCAGGCCATC	4688
rs553397152	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587395	GCCCAGGAGTTCAAG[A/T]CCAACCTGGGCAAAA	4688
rs553426087	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560513	GTTTTTAGATGAATG[G/T]TGGTGGGTGGTGGGT	4688
rs553452486	in-del	-/TAA	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183580661	CCAGCAAAATCCTCC[-/TAA]TAATTCCCTAGCCCA	4688
rs553483448	snp	C/T	0.00676609	0.0577691	intron-variant	NCF2	GRCh38.p7	1:183589212	ATTCTTTAAGGGACC[C/T]GGGGAGTCAACCACT	4688
rs553559645	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183573863	GGGAGGCCAAGGAGG[A/G]CAGATCACCTGAGGT	4688
rs553596694	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576190	GGGAAATGACTGGAA[A/G]GTCCCATGTGACAAA	4688
rs553644158	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589871	AGTACGACTAGGACA[A/G]CCTTCACAAAGGTGT	4688
rs553707134	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582957	GAGCAACACAAAAAC[A/G]TACGAAAGTGGGGAA	4688
rs553756551	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183569879	ATAGGCGTGAGCCAC[G/T]GTGCCTGGCCACTTC	4688
rs553776476	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580082	AGAGTCATAAGGAAC[A/G]GGTGCCAGTGTGGCT	4688
rs553810553	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557230	CCACCTACCTGACCA[C/T]ACAGCCAGTTCAGAA	4688
rs553961926	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587320	CAATAATTCCCAGGT[A/G]CGGTTGCTCACACCT	4688
rs553968031	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183557883	TACTACTACTCATAT[A/T]TTTTTTTTTGAGACA	4688
rs553969184	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574823	GTTAAGAAAACACCA[C/T]GGAATGCGTAAATGC	4688
rs554005946	snp	C/G	1.65094e-05	0.00287305	synonymous-codon	NCF2	GRCh38.p7	1:183567219	CTGCCCGTTGAACAT[C/G]ACCGTGGCCCAGTTA	4688
rs554009769	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558833	CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG	4688
rs554068546	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559661	GCCAGGAGTTTGAGA[A/C]CAGCCTGGTCAACAT	4688
rs554387517	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183577898	CTTGGGAATGGTGTT[A/C]CCCCCAGGGCTGTGC	4688
rs554493131	in-del	-/T	0.301932	0.244547	intron-variant	NCF2	GRCh38.p7	1:183561641	CTTTCTTTTCTTTTC[-/T]TTTTTTTTTTGTATT	4688
rs554511489	in-del	-/TCTTGC			intron-variant	NCF2	GRCh38.p7	1:183575679	AAGACATTGACACTG[-/TCTTGC]TCTTGGGTCACTTGC	4688
rs554727062	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591396	GTATTAATATGTTAG[G/T]GTTTATCTTGAGCTG	4688
rs554848021	snp	A/C			missense, intron-variant	NCF2	GRCh38.p7	1:183573206	CTTGCCTAGGTAATC[A/C]TTCTTGGCCAGCTGA	4688
rs554849993	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585871	TATTCCATGTTGACT[A/G]TAAACAAACCTAAAA	4688
rs554859199	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578306	TGCCTCCTCCCTACA[A/C]TTTGGAAAAGAAAAA	4688
rs554910050	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586249	TAAGCCAGGAGAATC[G/T]CTTGAGCCTGGGAGG	4688
rs554976181	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575442	CCTTCACCTCAGGTG[C/G]GGGGGGAATGGTAAA	4688
rs555051803	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183572296	TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCCAG	4688
rs555129171	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560675	GCTGCTGCTGATCTG[A/T]CAGGAGGCAGAGCTC	4688
rs555195940	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570393	ACCTCAGGCCCAGGC[C/T]CCACAGGGTTCCCCA	4688
rs555196083	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562817	CGACAGAGTGAGACT[C/G]CATCTCAAAAAAAAA	4688
rs555224741	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183590020	GACCAGTTAAATCAG[A/G]CTGTCTAGGGGTGGA	4688
rs555238676	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569650	CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT	4688
rs555317674	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588440	AGATTGCACCACTGC[A/T]CTCCAGCCTGGGTGA	4688
rs555476776	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183589509	AAAAAAATAATTATC[C/G]AGAATGCTTAACTCC	4688
rs555497007	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558689	CTTGCCTCAGCCTCC[C/G]TAGCAGCTGGGACTA	4688
rs555649211	in-del	-/TAACC	0.00119737	0.0244387	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555605	TATATGCCTTATGAG[-/TAACC]TAACCTATAAGGTTA	4688
rs555733201	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588392	AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCA	4688
rs555766151	in-del	-/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183581761	GAAGCTCCGCCTCCC[-/G]GGTTCACGCCATTCT	4688
rs555796950	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581689	GTTTTTTTTTTTTGA[A/G]ACAGAGTCTCGCTCT	4688
rs555812016	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183585491	TTAGCTGGACGTAGT[-/G]GCGGGCACCTGTAAT	4688
rs555936977	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557538	TTTGTAGATGAGACC[A/G]TCTCATAACTTGAAT	4688
rs555999377	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183581874	GGGTTTCACCGTGTT[A/T]GCCAGGATGGTCTCG	4688
rs556173415	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586411	TACTTATCTGTAGTA[A/G]TTTATTCTTATACAT	4688
rs556179173	snp	A/C/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183578220	CCACTGCCTTCGCCC[A/C/G]TGGCTTCTTTTGAGT	4688
rs556205743	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572147	ACTGCTGACTCACTT[C/T]AGACCATGTCTGAAA	4688
rs556255666	snp	A/G			missense	NCF2	GRCh38.p7	1:183565761	GAGCTGGGATGTCGG[A/G]CTGCGGAGAGCTTTC	4688
rs556389548	snp	C/G/T	0.000181211	0.00951716	synonymous-codon	NCF2	GRCh38.p7	1:183565765	TGGGATGTCGGACTG[C/G/T]GGAGAGCTTTCCTCC	4688
rs556588805	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563912	ACCCTCCCTTTGGGG[A/C]TCTTCCTATAATCCA	4688
rs556748175	snp	C/G	1.64784e-05	0.00287035	synonymous-codon	NCF2	GRCh38.p7	1:183556208	CTTCCCTTTGCACTC[C/G]CCTTCCAGCCATTCT	4688
rs556809073	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577844	TTTTGACCTGTTCTA[C/G]TTTTCAGCAACCCTG	4688
rs556850278	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183586806	AACAGAGGTTGGGAA[A/G]GTACTGCTCAAACAC	4688
rs556857621	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569805	ATGTTGGCCAGGCTG[A/G]TCTGGAACTCCTGGC	4688
rs556944587	snp	A/G	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183562704	TGGGTGCAGTGGCAG[A/G]TGCCTGTAATCCCAG	4688
rs556953668	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585706	TGGAACAGTTTCTAC[A/G]AAGGGTCAGTTTCCC	4688
rs556988673	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591911	TGAAAAATTGAAGAG[A/T]TGAAAGTCCTGCACT	4688
rs557168374	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591252	TGGCTTACAAAGTGA[C/T]GGAGAAAAAATCCTG	4688
rs557231718	snp	G/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183585038	GTCTGTGGTTTTTCT[G/T]TTAGAAAAGACTTCA	4688
rs557374618	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183569026	AAGCCTGACATTCCA[A/G]AAAATTCAACAAGAT	4688
rs557393783	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575357	CACCTGTAATCTCAG[A/C]TACTTGGAGGCTGAA	4688
rs557403513	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583322	GCCTCCTAAAGTGCT[A/G]GGATTACAGGTGTGA	4688
rs557437210	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574871	TCCAACAACGAAATA[A/G]GTCAGGAAGGGACAA	4688
rs557442392	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589924	TTAATTTAGAAGATG[C/G]AGAAAGAGGCAACCC	4688
rs557533783	in-del	-/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183564242	AACAAACTCAGTCTC[-/T]TGCTTCTAGGGAGCC	4688
rs557535861	snp	C/T	1.65002e-05	0.00287225	synonymous-codon	NCF2	GRCh38.p7	1:183567243	CCAGTTATCATTGCC[C/T]TTCTTCAAGACAAAG	4688
rs557539304	snp	C/T	0.00557542	0.0525036	intron-variant	NCF2	GRCh38.p7	1:183586226	GTAGTCCCAGCTACT[C/T]GGGAGGGTAAGCCAG	4688
rs557630200	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576294	AGGGCCATTTTAACC[C/T]CAACTCCAGGGGAAA	4688
rs557655005	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569591	TTTTTAAATTAATTT[A/T]AAAAAAATTTTTTTT	4688
rs557677753	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571468	TTTATCACATTCACA[A/G]TGCTGTGCAACTACT	4688
rs557691676	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576844	TGTCAGTGATTTTTC[A/T]AAAGAAAGGTCTTTG	4688
rs557696768	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183559803	GGGGGAGGTTGCAGT[A/G]AGCCGAGATTGTGCC	4688
rs557958791	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568035	CACTCTGTTACTTTC[A/C]CCTCGGCCCATCCTT	4688
rs558005352	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580866	TGCCTATAGTTCCAG[C/T]TACTCAGGAGGGTGA	4688
rs558122943	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566092	CAGGACTGAGCTCTT[A/G]TCTCCACTGCAGAGG	4688
rs558385596	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592691	TTAATTATTCCTGAG[A/G]AAACCAAATGGATTT	4688
rs558480614	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592188	CCCTAAAAGCCTGAA[A/G]ATAAAACTTAAAAAT	4688
rs558537040	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573012	TTGGAGAAAATAAAC[C/T]AGACATGGTTGCCTA	4688
rs558542835	in-del	-/T	0.2768	0.248559	intron-variant	NCF2	GRCh38.p7	1:183578355	TATAGTATTTCCTCC[-/T]TTTTTTTTTTCTTTT	4688
rs558599546	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556936	TTAAAAATGAAAGTT[A/C]TTTAGTAAACTTTCT	4688
rs558628541	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577787	TGAGTCTGCTTCTCC[C/T]TTCCCCATCTATTTC	4688
rs558830709	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586727	TTGCCTCCCCAGTGA[A/G]AGCTTCTGCCTCACC	4688
rs558896122	snp	A/G	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183579766	AAAAAAAAAAAAAAG[A/G]GAATAATAACAGCAT	4688
rs558950555	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560760	TGGAGGTTGGGGACC[C/T]CTGGGATAAATGAAA	4688
rs559012556	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183589618	AGTCAATCACAGTAC[A/C]ATTTCCTCTTGCCAG	4688
rs559131190	snp	A/G	3.29582e-05	0.00405931	intron-variant	NCF2	GRCh38.p7	1:183563386	CCCTCCTCCAGGCCA[A/G]CACAAGGTTCCCACT	4688
rs559310079	snp	A/C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571408	AGGCATGAGCCACCA[A/C/T]GCCCAGCCCAAATTA	4688
rs559406873	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575946	ATGAGCTACTGCCTT[C/G]TGAATTCGTTGGCTT	4688
rs559549522	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591077	TGGGGGGACTTTCCT[A/G]CCTTTGGGTAGGGGA	4688
rs559569338	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574428	TCAATGGCATGTCCT[C/G]TGAGACAAATGAGAA	4688
rs559903633	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581177	GTCCCAGCTACCCGG[C/G]AAGCTGAGGTTGGAG	4688
rs559933629	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183572682	TCTCAATCTGTTGCC[C/T]AAGCTAGAGTACAGT	4688
rs559936749	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575208	GGCGCAGTGGCTCAT[A/G]CCTGTAATCCCAGCA	4688
rs559997304	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567767	GCCAGAAAGATTGGT[A/G]GGAGAGGAGGAAGGA	4688
rs560208992	snp	C/G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579980	CATATAAGCTATTAT[C/G/T]AGGATATTTTAAAAA	4688
rs560290739	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183565159	AACCACTCACTCTGC[G/T]TCTCTACCAAGCGCT	4688
rs560524734	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183569606	AAAAAAAATTTTTTT[G/T]GAGATGGAGTTTCAC	4688
rs560588593	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564913	AAGTGTCACGAGTCT[A/G]TAACTTTTCAACTGG	4688
rs560601370	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579362	TTGAGTCTTGGCTCC[A/G]TCACTTACTATCTGG	4688
rs560729507	snp	A/C	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183581715	GCTCTGTTGCCCTGG[A/C]TGGAGTGCAGTGGCG	4688
rs560754812	snp	C/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183556091	ATAGGGCTTCATTTT[C/T]TTCAGCTTTGTAGTT	4688
rs560797217	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570116	CCCTGCTCAGAAAAC[C/T]GCCCTCTGCTAGTGC	4688
rs560823166	snp	C/T	3.29685e-05	0.00405995	missense	NCF2	GRCh38.p7	1:183563525	GCTGAGTCTTCATGA[C/T]TACCGTGTACTTGTA	4688
rs560826015	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183590922	AGAGTGAGAACTTCT[G/T]TTCCTGTTTGTCTGC	4688
rs560948583	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585286	CCACGCCCGGCCTCA[A/C]CCTCACCCCACCCAC	4688
rs561237111	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576364	ATAATCCTTTTTCTA[A/G]AGCCACTTGTCCCCC	4688
rs561340320	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561015	AAGGTGAATCCTGCA[A/T]TCTGTATTTTAAGTC	4688
rs561377969	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567674	GGCCAGCACCCAAGG[A/C]TGGGCTGGGGTGGGG	4688
rs561379130	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568527	TTCATCACTTTGAGA[G/T]AATTCTTAAGAAAGC	4688
rs561381689	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183575882	GGGGGCCAGGATCAA[C/T]CCCGGAAGTGGAAAT	4688
rs561501414	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561960	CCACCACACCCAGCT[A/C]ATTTTTGTATTTTCA	4688
rs561504327	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588772	ATGAGAAGGCTAGAA[A/G]CAGAGGAATGCCAGG	4688
rs561525294	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587535	GGAGGTGGAGACTGC[C/T]GTGAGCTGTGACGGC	4688
rs561556995	snp	A/G	0.0003255	0.0127532	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590393	AAGACAGGTTGGAGC[A/G]TCTCCCCTAGCAGGG	4688
rs561562359	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559143	CCTGAATCAGAATCT[C/G]TGGAGGGTGGGCCCA	4688
rs561666354	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589470	TCCAAACTCCATACC[C/T]TTTCCACCTTACCAC	4688
rs561720503	snp	C/G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559920	TGGCTACTAGAGCAA[C/G/T]AGACAGGGAAAGTCT	4688
rs561994305	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573453	GTGTTAAGGTAGGAA[A/C]CCTTGGTTTCAATAC	4688
rs562022512	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580364	CCAGAAATCAGGTTC[C/T]GCTTTCTAAGCCAGA	4688
rs562099929	in-del	-/T	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183557247	CAGCCAGTTCAGAAG[-/T]TTGTCTTTGTACATC	4688
rs562194389	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587548	GCCGTGAGCTGTGAC[A/G]GCACCACTGCACTCC	4688
rs562393614	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183583307	GATCCGCCTACCTTG[A/G]CCTCCTAAAGTGCTG	4688
rs562428154	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183556370	AAAGACAGTATTGCA[A/C]AGTGGTTTGAGAGTG	4688
rs562537763	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557365	AAAAGTTCCCTTAGG[C/T]AATTCTAACTGCAAA	4688
rs562538969	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572487	ATGCACAGCCAAGAC[C/G]TGGATTTAGAAGAAG	4688
rs562574374	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564236	ACACATGAACAAACT[C/G]AGTCTCTGCTTCTAG	4688
rs562576624	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570534	AGAGATGTGAAGACC[A/G]GCATTTGTGGGGAAG	4688
rs562577227	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571791	AAGCAGACATGGTCT[A/C]TGCTCTCTCAGTGCT	4688
rs562600947	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183580526	GGTCTCAGAGGGCAC[A/T]CACTTTAACTGCCGT	4688
rs562759045	snp	C/T	0.00398564	0.0444627	intron-variant	NCF2	GRCh38.p7	1:183558068	TTAGTAGAGATGGGG[C/T]TTCACCATGTTGGCC	4688
rs562771064	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183588116	AGTTTGAGTAGAGTA[A/C]AATTTTACTGTGAAA	4688
rs562798166	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555510	GGAATTGAGTGTTGT[A/G]GTCCATGAGAACCTA	4688
rs562923476	snp	A/G	0.00914312	0.0669923	intron-variant	NCF2	GRCh38.p7	1:183578408	TATTGCCCAGGCTGG[A/G]GTGCAGTGGTGGGAT	4688
rs562934185	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563099	CCCCAACACCACATA[C/T]AGTGCCTAGTACACA	4688
rs562938452	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570397	CAGGCCCAGGCCCCA[C/T]AGGGTTCCCCACTTG	4688
rs563118156	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555638	TCAAGCCTTAAGAGC[C/G]AATTACAGTAATGGT	4688
rs563212845	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569956	CCTCCCCTGTTCTAC[A/T]CTGAATACCATGGAA	4688
rs563249922	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183577192	CTGGCAGGTCCTGCA[C/T]GGACAATGAACTCAT	4688
rs563385063	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183584200	GACTTCATATCTATA[A/G]CCCCTGAATTGTACA	4688
rs563719478	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581732	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGG	4688
rs563751793	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575719	AGAGACGCCAGCTGC[C/T]ATGTCATGACAAGAC	4688
rs563780713	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573987	CCCAGCTACTTGGGC[A/G]GCTGAGGCAGCAGAA	4688
rs563789081	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582067	CCTCTCCACTTGTTT[A/G]CCCAGAGCTGCAGCC	4688
rs563789229	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575257	GGTGAATCACTTGAG[G/T]TCAGGAGTTTGAGAT	4688
rs563798337	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561851	CACCCAGACTGGAGT[A/G]CAGTGGTATGATATC	4688
rs563866671	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585816	GGGAGGAGGAATTGA[A/G]ATTAACTTTCATTTT	4688
rs563966610	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565932	GACATTTGGGGAAGA[C/T]GAAGGAAATGTTGGC	4688
rs564014096	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560874	TATTATTTCTTTACA[C/G]ATGGGGACAGAGCCC	4688
rs564030065	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558281	TTTGTTTTTGTTTTT[G/T]TTTTGAGACTGAGTC	4688
rs564166078	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557274	CATCTAGATCAGACA[G/T]TAAGGCACTGGTGCC	4688
rs564213584	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566615	AAGCAGACACACTTG[A/G]GAAGACCTAACCCAC	4688
rs564247013	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587772	CTTGACAATATGAAG[C/T]GCCTTCTTTGTAACT	4688
rs564293122	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183579497	TTTGGGAGACCGAGG[C/T]GGGTGGATCACGAGG	4688
rs564413289	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183586549	CAGTTTCATGATCAT[C/T]CCCATTCTGTGACAG	4688
rs564418799	snp	A/G	6.59033e-05	0.00573997	intron-variant	NCF2	GRCh38.p7	1:183573309	TGTAACACAGAAAAC[A/G]TAGCATTCCCTTATG	4688
rs564454200	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183580116	GGAGAAGCCATCACC[A/G]TTAGGGTTGAGGTAA	4688
rs564804545	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183556509	AAAGAAATTGAACAA[C/T]GAATCCTTAAATAGA	4688
rs564954493	snp	A/G	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183578507	TGAGCTGGGACTACG[A/G]GCGAGCGCCACCACG	4688
rs564973540	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570913	TCTCCCTCTTTGCTC[A/G]TGCCCTAGACCTGTT	4688
rs564976643	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183579459	AGGCCGGGCGCAGTG[G/T]CTCACGCCTGAAATC	4688
rs564976793	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183577120	AATCAAGTACATGGG[A/G]TAAGAACCATGGATA	4688
rs565037828	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564187	TAGTAAACTGTGGGG[A/G]AAATCTCGCCCTGGG	4688
rs565234906	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569780	TTTTAGTAGGGACAG[C/G]GGTTTCACCATGTTG	4688
rs565319719	snp	C/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183569239	ATGAGGGAAAGCAGG[C/G]GAGAGACAACAAACG	4688
rs565425853	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581811	TAGCTGGGACTACAG[A/G]CGTCCGCCACCGCGC	4688
rs565463586	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581467	AGTGAGACCCCTTCT[C/T]TAAAAAAAAAAAGAT	4688
rs565467777	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555295	CAACACGTTTCTCAG[A/C]TCATGTCTCCATTGT	4688
rs565737260	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568665	AACATCCACACAGGA[A/G]AAAGGACGTCATTCT	4688
rs565823302	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575353	CAGGCACCTGTAATC[C/T]CAGCTACTTGGAGGC	4688
rs565886350	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572969	GCTCTCACCCAGGGT[C/T]GAGCTGGAAGGGAGA	4688
rs566034328	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580452	GAAGCAGAGGTTTCC[A/T]GTTTCCTGGCAGCTG	4688
rs566176922	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183573615	CACCACGACAAGGCT[A/G]GCCCGGGATCAAGCA	4688
rs566394360	snp	A/C	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183586841	CCCGCAACACTGAGA[A/C]CCCTTGGGTTTCTCT	4688
rs566497433	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591088	TCCTGCCTTTGGGTA[A/G]GGGAACCACCCCTGC	4688
rs566572982	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556919	GCCATTGGTTAAATA[C/T]ATTAAAAATGAAAGT	4688
rs566647420	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579619	TGGTGGGCGCCTGTA[C/G]TCCCAGCTACTCAGG	4688
rs566654817	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183584743	CTGGAGACGGGGTAA[G/T]GGGGAGTGAGAAAGA	4688
rs566655129	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591778	ACAGGAGTGAGCCAC[C/T]GTGCCCAGCCGAAAT	4688
rs566660128	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557413	CTTACAGGGTAGGTC[A/G]TGGACTGGAAGCATA	4688
rs566674275	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183588331	TGAAACATCATTAGA[C/T]GGGCTTGGTGGTGCA	4688
rs566767089	in-del	-/TTTTTG	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183558258	TTTTTAATTTTAATT[-/TTTTTG]TTTTTGTTTTTGTTT	4688
rs566799386	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586632	GGGTGTCACACCAGC[G/T]GAGTATCAGGCCCAT	4688
rs566903361	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578196	TAGCTGCCACCATCA[C/T]CCTCCTGCCCACTGC	4688
rs567036655	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568848	TGTGGGTGGCTGTGC[A/T]CGTGGACAGAGGGCC	4688
rs567131378	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571862	AACATGTGGCCTTTC[A/G]TATCTGGCTTCCTTC	4688
rs567145856	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563808	ATCTGGCCCACTAGC[G/T]TGGGTAGTAGGAAGT	4688
rs567162829	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562435	GCCTTTTGTCTCAGC[C/T]AGAGACACCAGGGAG	4688
rs567264805	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183576549	CCACAACCCCTCTCT[C/T]GCCTCTGCTACAATA	4688
rs567536183	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589010	TCAGCCCCTCAGCAG[A/G]CCCCTGAGAGGAGGT	4688
rs567698233	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183586659	CCATGGTGGTTACCT[A/G]GGCTCATTGTGCCTA	4688
rs567710297	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567904	CCGTGGTGCAGTGTC[A/G]GTTCCCTTAAGTCTG	4688
rs567773372	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560381	CCTGGGATATAAACT[C/T]ATAAAGTTTGTGATC	4688
rs567940296	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183582852	TGGGGCTAGAGAGGC[A/G]AGACAGCTTGGCTGT	4688
rs567987908	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589860	GTGTAGAAGAAAGTA[C/T]GACTAGGACAGCCTT	4688
rs568092871	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183583297	GACCTCAGGTGATCC[A/G]CCTACCTTGGCCTCC	4688
rs568129868	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183564759	AAAACCTGTCAAGGA[C/G]ATTGAGCAGGAGCAA	4688
rs568201520	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572783	TAGCTAGGCTGGTCT[C/G]AAACTCCTGGCCTCA	4688
rs568249027	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183575331	AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT	4688
rs568321812	snp	G/T	0.0115144	0.0749975	intron-variant	NCF2	GRCh38.p7	1:183578739	CTGACTGGCTCGATG[G/T]ATACCAGGGCTGCTG	4688
rs568364678	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565447	GGGTTTGGTGACTAC[A/G]TGAGTCACTCAGGAA	4688
rs568365875	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574738	TTCTCCCTTTCTCAG[C/G]TCTCCTGGGAATATC	4688
rs568560099	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579522	ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	4688
rs568668596	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557795	CACCTTTAAAGTGGC[A/C]CTTGGAGGTGTTCAA	4688
rs568710134	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558392	CCTGCCTCAGCCTCC[C/T]GAATAGCTGGGATTA	4688
rs568830928	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556040	ATGTCTCAGTACAGT[A/G]TACAGCAGAAGGGTG	4688
rs568863002	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183572358	CCCAGCTAATTTTGT[A/G]TTTTTAGTAGAGATG	4688
rs568867705	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563666	CCGCAGTTTCGTGAT[C/T]TGGCACAGGGGGTAC	4688
rs568883428	snp	A/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183563313	GGCCGATAGCTGGGT[A/G]GGGATAATGAGTAAG	4688
rs568954675	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585822	AGGAATTGAGATTAA[C/T]TTTCATTTTGAATTT	4688
rs569044791	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592003	CCAGAAAAGTAAAAA[C/T]CAGTAAAACCTCCCA	4688
rs569066521	snp	A/G	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183556726	TAGAGACAGGATCTC[A/G]CCATGTTGCTCAGGC	4688
rs569068647	snp	C/T	0.0166325	0.0896639	intron-variant	NCF2	GRCh38.p7	1:183570313	GGTTCACTCTCAGTG[C/T]GCTGCCTGTGTTCCC	4688
rs569329273	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583876	GAGATTGCTTTTTTT[A/T]AATTTTTTTTTATTT	4688
rs569365439	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590556	AACCCTACCATGAGA[A/G]AGAAAAGGAAAGAAG	4688
rs569432064	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575411	AAGACAGAGGTTAGC[A/C]CAGAAGCCAGGGGCA	4688
rs569559514	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183568745	CAGCCAGTGCGAAAC[C/T]GATCTCCAACCTGAG	4688
rs569596664	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581851	TTTTTGTGTTTTTAG[C/T]AGAGCCAGGGTTTCA	4688
rs569623376	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183569258	AGACAACAAACGGCT[A/G]ATGGTAATTTGAGCA	4688
rs569675289	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582671	ACAGAGGTTTGGGCC[C/T]ACTCCCTTTCCTGTT	4688
rs569819586	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562382	ACTTCCAAGAGACCC[A/C]TTACACTCACACTCA	4688
rs569958369	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591735	AGGTGATTCGGCCTC[C/T]TCGGCCTCCCCTCAA	4688
rs569997541	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566111	CCACTGCAGAGGGCA[C/T]TGAGAAAGGAAAAAT	4688
rs570028783	snp	C/G	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183587509	TGAGGTAGGTCAATC[C/G]CTCAAGCCCAGGAGG	4688
rs570300909	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183571652	AGATGTAAAGCTAGC[C/T]TTATTCACAAATATG	4688
rs570377855	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183578367	CTCCTTTTTTTTTTC[-/T]TTTTTTTTGAGACAG	4688
rs570450559	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183559508	TCCAGCCCAATTTGT[C/T]ACCTCTGGGAATGAG	4688
rs570505900	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557588	TCCTACCCTGACCGC[C/T]AAATTCTGTTTTCTG	4688
rs570586237	snp	A/G	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183587261	TACCATCTGATTTCT[A/G]CTTTTGTTAGTCATA	4688
rs570742962	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183573667	TGGATGGGTGTTTGC[A/T]GATGAGGATAGACAT	4688
rs570783747	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580607	ATGGATTTCAGCTGG[A/G]AAGTGACACCACCTG	4688
rs570789434	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592443	TACCCAAAAACTTGC[A/G]TCATACTTACTGCAA	4688
rs571008549	in-del	-/A	0.00478085	0.0486577	intron-variant	NCF2	GRCh38.p7	1:183576416	GGCTGTCATTGGCTT[-/A]TTAGCAATGTCTGGA	4688
rs571016117	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575272	GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT	4688
rs571075293	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564450	GTATGTTTCCTAAAG[C/T]TTATTAATTTAATCT	4688
rs571103814	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565248	GCCTTTCAGAGAGAA[C/G]ATTTCCATTTCACAT	4688
rs571175552	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569469	TCACACAGCAACATG[A/G]TGTCACAAGAATGCT	4688
rs571212408	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555902	CCTCTCCCCTAACTC[C/T]TCCATTCACCTGTCC	4688
rs571272131	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570214	CCTCTTTCCTTCACA[A/G]GGAAGCTCTGTGTGC	4688
rs571292627	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183581085	AAGACAGGGTGGACC[C/T]GCCTAGGCAATATGG	4688
rs571448413	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591871	AGCCACATGACAGTG[A/G]ATTATGACTTCTCCC	4688
rs571460195	snp	A/G	0.000313456	0.0125152	missense	NCF2	GRCh38.p7	1:183563560	ACCTTGAGTGTGTAG[A/G]GCATGGGAACACTGA	4688
rs571551582	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591191	TCCTGCAGCAGGTAG[A/T]GTGGCCCACTGAGGC	4688
rs571619733	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561003	AGAAACTCCCTGAAG[A/G]TGAATCCTGCAATCT	4688
rs571671633	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580806	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4688
rs571709075	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561188	TGAAGGAGAAGGATG[C/T]GGTTTCTACAGATGT	4688
rs571813523	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589905	AGACACTTGTAGAAT[A/G]ATTTTAATTTAGAAG	4688
rs571961178	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577495	GAGGCAAAATGGCTT[C/T]TCCAAGCTCCTGGAG	4688
rs571997839	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583777	AGGATGCATGAGTGG[A/G]TGGCAGCAGCTGGAC	4688
rs572063958	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183564932	CTTTTCAACTGGCTC[A/G]GGGGAGAAAAATAGA	4688
rs572097759	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566584	CCAGCCAACACATTG[A/G]CTACTCTTCCACGTG	4688
rs572135292	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183573906	ACCTGCCTGGCCAAC[A/G]TGGCAAAACCCCGTC	4688
rs572185369	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557939	GGGTGCAAAGGTGCA[A/G]TCTTGACTCACTGCA	4688
rs572224337	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557255	TCAGAAGTTTGTCTT[C/T]GTACATCTAGATCAG	4688
rs572292378	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183561767	ATTTCAGGCATAAAC[C/G]ATACCAGGCCTCTTT	4688
rs572351199	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183558275	TTGTTTTTGTTTTTG[-/T]TTTTTTTTTTGAGAC	4688
rs572564154	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183587321	AATAATTCCCAGGTG[C/T]GGTTGCTCACACCTG	4688
rs572803994	snp	C/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183572163	AGACCATGTCTGAAA[C/G]AATTTAAGACTTGGA	4688
rs572854374	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591602	ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG	4688
rs572906223	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590625	AGAGAGGAAGTACAT[C/T]AGCTGCTGCCTGAAG	4688
rs573012770	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592148	TGTAGCAACTGAAAG[A/T]ATTCACTCATTATCA	4688
rs573076148	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585894	ACCTAAAAATGCAGA[C/T]AGGGTGATAGAAGAA	4688
rs573085574	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572310	CTGCCTCAGCCTCCC[A/T]GGTAGCTGGGATTAC	4688
rs573191136	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583410	CTCTAGCCCCCATCC[C/T]GCTTACTTAAAACTA	4688
rs573207861	in-del	-/A	0.00993419	0.0697739	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555600	ATTTGTATATGCCTT[-/A]ATGAGTAACCTATAA	4688
rs573245754	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183569652	GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC	4688
rs573272606	in-del	-/A	0.439363	0.163222	intron-variant	NCF2	GRCh38.p7	1:183580978	GCGAGACTCCAACTC[-/A]AAAAAAAAAAAAAAG	4688
rs573324544	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183582753	CATGGAATGGGTCTC[A/G]CCCTTATTGTCATGC	4688
rs573336431	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570399	GGCCCAGGCCCCACA[A/G]GGTTCCCCACTTGCC	4688
rs573415036	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560695	AGGCAGAGCTCAGGC[C/T]AGTATACCTGCAGCT	4688
rs573636389	snp	A/T	3.29544e-05	0.00405908	intron-variant	NCF2	GRCh38.p7	1:183590128	ACAAATGCACAGAGG[A/T]GGCCCGGAAAGAGGC	4688
rs573981459	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567713	GTGACTGTGGTCAGG[C/G]GAACAGCACAAAGCA	4688
rs574011269	snp	C/T			utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590587	CAGAGAGAGAGAGGG[C/T]GAGTAGGGGTGGAGT	4688
rs574021024	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575765	GAGAAGTTCATGTAG[C/T]GAAGAACTGAGGCCT	4688
rs574066971	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557557	CATAACTTGAATGCA[A/G]TTGAACTCCCCTCTG	4688
rs574126016	in-del	-/TGTT	0.296619	0.245615	downstream-variant-500B	NCF2	GRCh38.p7	1:183555503	CTCTGTGGAATTGAG[-/TGTT]TGTTGTAGTCCATGA	4688
rs574209474	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183585513	ACCTGTAATCCCAGC[A/T]ACTTGGGAGGCTGAG	4688
rs574228082	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183587635	AAAAAATCCAATGAT[A/G]CAAATAAAGACAAAG	4688
rs574241652	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575443	CTTCACCTCAGGTGG[G/T]GGGGGAATGGTAAAT	4688
rs574302512	snp	C/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183575203	GGCCAGGCGCAGTGG[C/G]TCATGCCTGTAATCC	4688
rs574318520	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183579338	CTTCTGGAGTCAAAA[A/C]CACCTGGTTTGAGTC	4688
rs574451768	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183571409	GGCATGAGCCACCAC[A/G]CCCAGCCCAAATTAA	4688
rs574504000	snp	A/C	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183579970	AGCTCCGTGCCATAT[A/C]AGCTATTATCAGGAT	4688
rs574576584	snp	G/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183564652	TCCAGTCCTAAAATA[G/T]CAGAGCCAGTAGCCT	4688
rs574644721	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573817	TATTTTAGGCAGGTG[C/T]GGTGGCTCATGCCTG	4688
rs574809811	snp	A/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183566287	TCAGATCTGACAAAG[A/T]CAGCTCTCTAGGCCT	4688
rs574823043	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556311	TTCCACACAGAATTT[A/G]TTATCTGTCACCCTT	4688
rs574837574	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592770	ATCCCACCCTGACAC[G/T]CAGAACTCTCCTTAA	4688
rs575180424	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183570535	GAGATGTGAAGACCG[A/G]CATTTGTGGGGAAGC	4688
rs575308641	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555227	TGGTAACCTAGCTGT[A/G]TAGTAGGCTATACCA	4688
rs575492608	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578283	GTTTCCTCACCGCCC[A/G]CCACTTCTGCCTCCT	4688
rs575518697	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591388	CATAGGCTGTATTAA[C/T]ATGTTAGTGTTTATC	4688
rs575529899	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183585762	ACTTAGAATTTTTTT[C/T]CTTTGTTATTTGTTA	4688
rs575616716	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183581995	TTTTAAACATGTCTC[C/T]GAAAGCACCGGCCTG	4688
rs575682354	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583355	CACTGTGCCCAGCCA[A/G]TCTGAGGGAATTTCT	4688
rs575834391	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183562717	AGGTGCCTGTAATCC[A/C]AGCTACTCAGGAGGC	4688
rs575870163	snp	C/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183569036	TTCCAGAAAATTCAA[C/G]AAGATTTAGACCCTG	4688
rs575916319	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561883	GCTCACTGTAACCTC[C/T]GCCTCCTGGGTTCAA	4688
rs576038948	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183568094	GGGAATACAGGCCCT[C/T]CCAGCTGACAGGGAG	4688
rs576111074	snp	G/T	1.65408e-05	0.00287578	intron-variant	NCF2	GRCh38.p7	1:183567365	AGAGGATAGACACAA[G/T]ATCCAGCCCCCATCC	4688
rs576138429	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570428	CCCCTGTACTCAAGA[A/G]GAGGCTTTGTTAATA	4688
rs576203825	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560605	AAGAGCATGCGACCT[A/G]GATCCCTTGCATGCA	4688
rs576253354	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183572963	CCTGTGGCTCTCACC[C/G]AGGGTCGAGCTGGAA	4688
rs576323003	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581596	AGCCTCCCAAAGTAC[A/C]AAGACTGCAACTGTG	4688
rs576360037	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183580869	CTATAGTTCCAGCTA[C/T]TCAGGAGGGTGAGGC	4688
rs576429686	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557982	CTAGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC	4688
rs576466263	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558627	CTGGAGGGCAGTGGT[G/T]CAATCTCGGCTCACT	4688
rs576470809	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582046	CTGCTGCAGGCCTCT[C/T]TTCGGCCTCTCCACT	4688
rs576733059	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586013	AAATGGGACTATGCT[A/G]TATGAACTGTTTTGA	4688
rs576746071	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592693	AATTATTCCTGAGAA[A/T]ACCAAATGGATTTGT	4688
rs576906858	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586334	AGTGAAACTCTGTCT[C/T]GGAAAAAGAAAAAAA	4688
rs577011641	snp	C/G	0	0	intron-variant	NCF2	GRCh38.p7	1:183579192	CAGCTCTGCCACTAA[C/G]TGGGGGACCCTAGCA	4688
rs577044494	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578510	GCTGGGACTACGGGC[A/G]AGCGCCACCACGCCC	4688
rs577047600	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557301	TGCCTGGATCCTGCC[C/T]CCAGAAATTTTGCTT	4688
rs577069132	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572368	TTTGTATTTTTAGTA[A/G]AGATGGGGTTTCACC	4688
rs577073418	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183579804	ACAGGTTCATTGTGA[A/G]AACTAAAGGAGATGA	4688
rs577173442	snp	G/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183561717	ACTCCTGACCTCAGG[G/T]GATCTGGCCCATCTC	4688
rs577230085	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573101	GCCACAAGGAGGCTA[A/C]CCTCTTCTCAAGAGT	4688
rs577288508	snp	A/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183570531	TTTAGAGATGTGAAG[A/T]CCGGCATTTGTGGGG	4688
rs577354715	in-del	-/CTCACCAACCCACAAGGTTAGCAGGGAT	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183564287	AAGGACCAGCATATC[-/CTCACCAACCCACAAGGTTAGCAGGGAT]CTCACCAACCCACAA	4688
rs577412096	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563876	CTAGCTCATGGACTC[C/T]GTAAGGTAGCAACTG	4688
rs577738410	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590824	AGATAGGGGCAGGTC[A/C]CTGGTGAAACCCCAC	4688
rs577899872	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560810	ATATACAGTCTTAAA[A/C]TATCTTACTGAAACC	4688
rs577962758	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183589902	TAAAGACACTTGTAG[A/C]ATGATTTTAATTTAG	4688
rs578051001	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588530	ATAATGAAATTTTAA[A/C]CCTTGTTGCATTTCT	4688
rs578107077	snp	A/C			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555760	ACACAGAAAAGTGCA[A/C]CAAATGTACAGCTTG	4688
rs578154138	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585580	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	4688
rs578169887	snp	G/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183581721	TTGCCCTGGCTGGAG[G/T]GCAGTGGCGCGATCT	4688
rs578257172	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576210	CATGTGACAAAGAGG[G/T]CCTTAGACCCTGAAA	4688
rs745334269	snp	A/C/G	3.29518e-05	0.00405894	missense, synonymous-codon	NCF2	GRCh38.p7	1:183563201	TGCACTCACCACTGT[A/C/G]TTCTCACACCACAGA	4688
rs745372047	snp	A/G	0.000626577	0.0176889	synonymous-codon	NCF2	GRCh38.p7	1:183570804	CAGAGGGGCAAACCC[A/G]GAGAAACTGTCTTGA	4688
rs745458881	snp	A/G	1.65031e-05	0.00287251	missense	NCF2	GRCh38.p7	1:183563567	GTGTGTAGGGCATGG[A/G]AACACTGAGCTTCAC	4688
rs745516007	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183573887	CTGAGGTCAGCAGTT[C/T]GAGACCTGCCTGGCC	4688
rs745524069	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183560892	GGGGACAGAGCCCTA[A/C]GTCAAAACTGGCTTT	4688
rs745532316	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574693	GGGAAAGGCTCACAC[A/G]TATACTCTGAGAATG	4688
rs745648528	snp	C/T	1.65138e-05	0.00287343	intron-variant	NCF2	GRCh38.p7	1:183567156	CAGAGACTGCATTTG[C/T]TGCCAGGATCCCATG	4688
rs745650507	snp	C/G	3.32447e-05	0.00407691	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556096	GCTTCATTTTCTTCA[C/G]CTTTGTAGTTTGTGA	4688
rs745691949	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183569375	CTGGGAAATAACACC[G/T]CCCACCAGCTCCCCA	4688
rs745740745	snp	C/T	0.000247119	0.011113	missense	NCF2	GRCh38.p7	1:183556198	AAATGCCCACCTTCC[C/T]TTTGCACTCCCCTTC	4688
rs745741272	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183580462	TTTCCTGTTTCCTGG[A/C]AGCTGCAATTTCCAC	4688
rs745752489	snp	C/T	1.64738e-05	0.00286995	missense	NCF2	GRCh38.p7	1:183590229	ATCCGGGAGTGGGGG[C/T]CCTGGACGGCACTGA	4688
rs745823727	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183580302	CATGTCTTTTCCACG[A/C]ATCTTTCTGGGTTCC	4688
rs745844166	snp	G/T	1.65622e-05	0.00287764	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590332	CCACCAGGGACATGA[G/T]TAGGTAGAAACTAGG	4688
rs746011169	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575840	GGATTGATGTTTCTG[C/T]GGCATTAGTGGCTGG	4688
rs746071691	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556283	ACTGTAGGAAGATTA[C/T]CCTGTCTGGCTATTC	4688
rs746117032	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584798	GCAGTTAGAGGCAAG[A/G]CGTCGGTCAAGATAA	4688
rs746128644	snp	G/T	3.29582e-05	0.00405931	intron-variant	NCF2	GRCh38.p7	1:183566908	ATGGGTCAGGCCTTG[G/T]CATCACATTACCTGG	4688
rs746214657	snp	C/T	1.66363e-05	0.00288407	intron-variant	NCF2	GRCh38.p7	1:183567391	CATCCCCTCACATGA[C/T]GCCATGGCGCAAATA	4688
rs746234611	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183583052	TTTGTAATCTGAGGG[A/T]ATTCCTTTTTTTTTT	4688
rs746326365	snp	C/T	2.19681e-05	0.00331415	intron-variant	NCF2	GRCh38.p7	1:183567492	TGACACTGAGCCTGC[C/T]TGGGCTCCCAAGAGG	4688
rs746333694	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183574746	TTCTCAGCTCTCCTG[C/G]GAATATCTAAAATAT	4688
rs746336607	in-del	-/TC	1.64838e-05	0.00287083	frameshift-variant	NCF2	GRCh38.p7	1:183556125	GAAACATCCTAGACT[-/TC]TCTCCGAGTGCTTTC	4688
rs746358104	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183576737	CATATGTCCCCAGGG[G/T]CCGAGGGCGGCTACA	4688
rs746362350	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564372	ATCGGAGTGCAAGGT[A/G]AGCCAGAGGCCACAG	4688
rs746391358	in-del	-/A	1.65138e-05	0.00287343	intron-variant	NCF2	GRCh38.p7	1:183567012	CAGCACCACAGAATC[-/A]GAAAGGAAAAAATAA	4688
rs746501134	snp	A/G	3.97212e-05	0.00445634	intron-variant	NCF2	GRCh38.p7	1:183567541	GTACACCTGCTCATA[A/G]CCATATATGCAGAGG	4688
rs746547879	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183559624	AGTACTTTAGGAGGC[C/T]GAGGCAGTTGGATCA	4688
rs746571661	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183573681	CTGATGAGGATAGAC[A/G]TATAAAGACTGGCTT	4688
rs746600651	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584506	TTACTTTTAGAAGTT[C/T]CCAAGATCTTTCTAA	4688
rs746618335	snp	C/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183569194	CAGCTGCCTATTGAA[C/T]ATTCAGGAGAAGTGA	4688
rs746666511	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183572297	TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCAGG	4688
rs746675636	in-del	-/TTTTTTTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561780	ACCATACCAGGCCTC[-/TTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4688
rs746692621	snp	A/G	1.64798e-05	0.00287047	missense	NCF2	GRCh38.p7	1:183563456	TAGTGTGTTCCAGCC[A/G]GAGCTCCAGTTTCTT	4688
rs746883471	in-del	-/A			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555791	TGAATGTTTACAGTG[-/A]TGAACACAGCTGGCT	4688
rs746894602	snp	C/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591381	GTAATCCCATAGGCT[C/G]TATTAATATGTTAGT	4688
rs746942426	snp	A/C/G	3.35577e-05	0.00409609	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556069	TGCTAAATCTTACAA[A/C/G]CAAGTAATAGGGCTT	4688
rs746971202	snp	A/G	6.58924e-05	0.0057395	intron-variant	NCF2	GRCh38.p7	1:183586986	TAAAGGCCTGAGGAG[A/G]GAAGGGTCCAGACAT	4688
rs747039614	snp	A/C			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555952	GCCCCAGGAAATCAT[A/C]CTGGGTACTCACATC	4688
rs747061831	snp	C/G	1.64939e-05	0.0028717	intron-variant	NCF2	GRCh38.p7	1:183563152	ATTGTTGAGGAAGTG[C/G]CTCAGTGGAAATGTA	4688
rs747131264	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587131	TGTGCTCTCACGGTG[C/T]ACCCCACTTCGCTCT	4688
rs747187964	snp	C/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183573167	GAGACTCAGGGGAAG[C/T]TGAGCAATCCCACCT	4688
rs747217995	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183565866	ACCCCTACAGAGACC[C/T]CATGTAAAGGAGCCA	4688
rs747231701	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568642	GCATGTGCCGATAGG[A/G]AGTGGAAAACATCCA	4688
rs747272727	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant	NCF2	GRCh38.p7	1:183573274	CAGGGATCACCACTG[A/G]CTCATATAGCTTCTG	4688
rs747282867	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589135	CAGTCACTTCTCTGT[C/T]TTCCTGTCAGGAGGG	4688
rs747384636	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183575253	GGCGGGTGAATCACT[A/T]GAGGTCAGGAGTTTG	4688
rs747445088	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183564279	TAATTACCAAAGGAC[C/G]AGCATATCCTCACCA	4688
rs747462402	snp	A/T	1.64868e-05	0.00287109	missense	NCF2	GRCh38.p7	1:183567275	CAATGTTCCCTGGCA[A/T]GACCTGGAGCTCTTC	4688
rs747548282	snp	A/G	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183560224	GTTGTCTGGTTATTA[A/G]CATCAGCTTTTTCAC	4688
rs747550232	snp	A/G/T	3.3231e-05	0.0040761	intron-variant	NCF2	GRCh38.p7	1:183567387	CCCCCATCCCCTCAC[A/G/T]TGATGCCATGGCGCA	4688
rs747647949	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570912	GTCTCCCTCTTTGCT[C/T]ATGCCCTAGACCTGT	4688
rs747657440	snp	A/G	1.64735e-05	0.00286993	intron-variant	NCF2	GRCh38.p7	1:183586881	TCCAGTTGGTGCAAC[A/G]TTGAACCACTTACTT	4688
rs747705788	in-del	-/AAAAATAC			intron-variant	NCF2	GRCh38.p7	1:183562671	AACCCCGTCTCTACT[-/AAAAATAC]AAAAATTAGCTGGGT	4688
rs747747590	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565552	GTGGGTGGTGCAGGA[A/G]AGGGGGATTCTGGGG	4688
rs747834710	snp	A/T	3.2021e-05	0.00400118	intron-variant	NCF2	GRCh38.p7	1:183567527	AGCAAGAAACTGGTG[A/T]ACACCTGCTCATAAC	4688
rs747962917	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584707	GGATTTGTTGTTAGG[C/T]CTCCCTGCATATTCT	4688
rs748058943	in-del	-/TTTGTA			intron-variant	NCF2	GRCh38.p7	1:183561964	CACACCCAGCTAATT[-/TTTGTA]TTTTCAGTAGAGATG	4688
rs748095453	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183557712	AAGGTTGTTTTAGTG[G/T]GTTCTTTCATTGTAT	4688
rs748182758	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568365	AGACATGGGGTTTTG[C/T]CACGTTGGCCCGGCT	4688
rs748228594	snp	C/T	1.64936e-05	0.00287168	missense	NCF2	GRCh38.p7	1:183567254	TGCCCTTCTTCAAGA[C/T]AAAGACAATGTTCCC	4688
rs748243328	snp	C/T	1.64811e-05	0.00287059	intron-variant	NCF2	GRCh38.p7	1:183560053	TTGACCTTGTTTCTG[C/T]TAACATGTAAATTTG	4688
rs748277308	snp	G/T	1.77313e-05	0.00297747	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590357	ACTAGGAGGCCAAGA[G/T]AGCTGCCAGGAGACA	4688
rs748362510	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183577760	ATGGAGAAATAAATG[A/C]AGCATAAAATGTGAG	4688
rs748376861	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183567073	ACAGCCCAGAGTCCT[C/G]GGGAAGGGATGACGA	4688
rs748378906	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578537	GCCCGGCTAATTTTT[C/T]ATATTTTAAGTAGAG	4688
rs748429825	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183569018	TCTAGAAGAAGCCTG[A/G]CATTCCAGAAAATTC	4688
rs748489095	snp	C/T	1.64991e-05	0.00287215	missense	NCF2	GRCh38.p7	1:183563557	TGCACCTTGAGTGTG[C/T]AGGGCATGGGAACAC	4688
rs748584833	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183574990	AGTGACTTGCTCAAG[G/T]CCCCTTCTAGAGGCA	4688
rs748619343	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574610	ATACATGAAAGCAAT[A/G]TTATATAACACCTAG	4688
rs748707281	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	NCF2	GRCh38.p7	1:183577608	CCTTACCTCACAGGC[A/G]AACAGCTTGAACTGG	4688
rs748898061	snp	C/T	1.64746e-05	0.00287002	missense	NCF2	GRCh38.p7	1:183577657	TCTATCAGCTGGTTC[C/T]CTCGAAGCTGAATCA	4688
rs748908918	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183564064	GAGTAAAACAAAAGA[A/T]GATGGTGAATGAACA	4688
rs748980334	in-del	-/AT			intron-variant	NCF2	GRCh38.p7	1:183563095	TATCCCCAACACCAC[-/AT]ATATAGTGCCTAGTA	4688
rs749065525	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	NCF2	GRCh38.p7	1:183560187	TGCCTCCACTTGGCT[A/G]CCTTTCTTAAGCTGA	4688
rs749109356	snp	A/C	1.67393e-05	0.00289299	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590343	ATGATTAGGTAGAAA[A/C]TAGGAGGCCAAGAGA	4688
rs749130837	snp	G/T	4.38375e-05	0.00468154	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590429	TTAGTGGCCCCCAAG[G/T]TGTTCACTTTCTGGG	4688
rs749187972	snp	A/T	1.64933e-05	0.00287165	missense	NCF2	GRCh38.p7	1:183570819	AGAGAAACTGTCTTG[A/T]TCCACCACAGATGCC	4688
rs749232924	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183583166	CAAGCTATTCTCCTG[C/G]CTCAGCGTCCCAAGT	4688
rs749249406	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570686	GAAGGAGCCCTTACA[A/G]TCAGGCAACTCAGCA	4688
rs749319711	snp	A/C	1.64738e-05	0.00286995	stop-gained, intron-variant	NCF2	GRCh38.p7	1:183574582	CAGCTTTTTTCCATT[A/C]CTCCTTCTTGGCATA	4688
rs749332139	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183572427	GACCTCGTGATCCAC[A/C]TGCCTCAGCCTCCCA	4688
rs749367579	snp	C/T			missense	NCF2	GRCh38.p7	1:183577643	CCAGGATCTTATAGT[C/T]TATCAGCTGGTTCCC	4688
rs749410546	snp	C/T	1.65162e-05	0.00287365	intron-variant	NCF2	GRCh38.p7	1:183567168	TTGCTGCCAGGATCC[C/T]ATGCCCATCGCACCA	4688
rs749472654	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183583138	GTTCACTGCAACATC[C/T]GCCTCCCAGGTCCAA	4688
rs749532381	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591031	CCCCTCCCCTATTCT[A/G]AGCCCATAAAAGCCC	4688
rs749546475	snp	C/T	1.64776e-05	0.00287028	missense	NCF2	GRCh38.p7	1:183556209	TTCCCTTTGCACTCC[C/T]CTTCCAGCCATTCTT	4688
rs749606885	snp	A/C	4.94197e-05	0.00497066	missense	NCF2	GRCh38.p7	1:183563305	TGTCCCGAGGCCGAT[A/C]GCTGGGTGGGGATAA	4688
rs749848761	snp	A/G	1.64732e-05	0.0028699	intron-variant	NCF2	GRCh38.p7	1:183574481	CTGCATCACCAATAC[A/G]CTTACCCAGACACAC	4688
rs749870624	in-del	-/TT			intron-variant	NCF2	GRCh38.p7	1:183584385	GAGATTAGTGCCTCA[-/TT]TTTGTATAATTTCCT	4688
rs749895398	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183575546	CACAATTTACACACA[C/G]AATCAAATAATCGTT	4688
rs749907634	snp	C/T	1.6477e-05	0.00287024	intron-variant	NCF2	GRCh38.p7	1:183560291	GAAATAATAAAGGGC[C/T]TGTTAATTTTCCCAA	4688
rs750044702	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566165	TTGAAGCTTTTCAAA[A/G]CATTTGGATATGGTG	4688
rs750050717	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183557481	ATCCATTTAGGAAGA[-/T]TTCGCAGGTGATTCA	4688
rs750073492	snp	A/G	1.64741e-05	0.00286998	intron-variant	NCF2	GRCh38.p7	1:183563993	TGAAACAGTATGAGG[A/G]AAAAATGTTACCTTA	4688
rs750080716	snp	C/T			downstream-variant-500B	NCF2	GRCh38.p7	1:183555362	ACAAGATACTACTTA[C/T]GAACTAGCTTCATGA	4688
rs750131635	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183573228	GCCAGCTGAGCCACT[C/T]GTCTCTCATTTGGTC	4688
rs750160959	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183556731	ACAGGATCTCGCCAT[C/G]TTGCTCAGGCTGGTC	4688
rs750171466	snp	A/C	1.64955e-05	0.00287184	intron-variant	NCF2	GRCh38.p7	1:183577564	CCATCCAGCCATGAT[A/C]CCCTCCTGCCCAGGC	4688
rs750200420	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568739	GGACTGCAGCCAGTG[C/T]GAAACCGATCTCCAA	4688
rs750235630	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592605	GTAAATGACCTGCAG[A/G]TAGCAGTGATGGCAG	4688
rs750285424	in-del	-/TTTTTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561782	CATACCAGGCCTCTT[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4688
rs750380443	snp	A/G	1.64906e-05	0.00287142	missense	NCF2	GRCh38.p7	1:183567326	CAAATAGCACACGGT[A/G]AGCCTCCCCTTCCAG	4688
rs750384875	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	NCF2	GRCh38.p7	1:183560154	GTCCTCTGGTTGGGT[A/G]GCCTCATAACTGAAG	4688
rs750490687	snp	A/G	5.08427e-05	0.0050417	intron-variant	NCF2	GRCh38.p7	1:183570736	AATGCTTCACAGAAA[A/G]CTCTCGAGACCTAGG	4688
rs750614636	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571667	TTTATTCACAAATAT[A/G]CTTAAACTATAGATA	4688
rs750697066	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574552	TCATGCTCGTGGCCA[A/G]TGCTAACTGTTCTTC	4688
rs750713969	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578187	CCCTTCTTATAGCTG[C/T]CACCATCACCCTCCT	4688
rs750743074	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578939	AGCAGGCATAAGCTA[C/T]GCCAGCCTCACTCCA	4688
rs750767231	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566601	TACTCTTCCACGTGA[A/G]GCAGACACACTTGGG	4688
rs750782115	snp	A/G/T	3.29458e-05	0.00405857	synonymous-codon, stop-gained	NCF2	GRCh38.p7	1:183586956	CCAAGTGCTTGTCTC[A/G/T]GTTAATGCTTCTGGT	4688
rs750810925	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560421	TGTAGAGCTTATATG[C/T]TCTTTATGAATACTG	4688
rs750867967	snp	A/G	1.64754e-05	0.00287009	intron-variant	NCF2	GRCh38.p7	1:183590140	AGGAGGCCCGGAAAG[A/G]GGCACCTCCACTCAC	4688
rs750881920	in-del	-/AAAAAAAAAAA			intron-variant	NCF2	GRCh38.p7	1:183585624	GCGAAACTCCGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAT	4688
rs750909999	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591738	TGATTCGGCCTCCTC[A/G]GCCTCCCCTCAAAGT	4688
rs750922183	snp	C/G	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183569164	TCTCTGGGGTTTTCG[C/G]TCTGGGTGGAGGCTC	4688
rs750954204	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577391	TAATAAAATGTATGC[C/T]CCCAGGTAACTGATG	4688
rs751011909	snp	C/T	3.30311e-05	0.0040638	intron-variant	NCF2	GRCh38.p7	1:183567196	CCAGCCCCTGATCCT[C/T]TGCATACCTGCCCGT	4688
rs751047769	snp	A/C			downstream-variant-500B	NCF2	GRCh38.p7	1:183555101	TTGCTGACCTTCTCT[A/C]TGTTTGTTTACACTG	4688
rs751096649	snp	C/T	1.64746e-05	0.00287002	missense	NCF2	GRCh38.p7	1:183560120	ACACCAGGATTATAT[C/T]CCCTTCCTGAAACTC	4688
rs751114991	snp	C/T	1.65108e-05	0.00287317	synonymous-codon	NCF2	GRCh38.p7	1:183590318	GAGGCTGATGGCCTC[C/T]ACCAGGGACATGATT	4688
rs751204541	snp	A/G	1.65833e-05	0.00287948	intron-variant	NCF2	GRCh38.p7	1:183570762	CTAGGTCCATGGAGA[A/G]GGTCAGGACTGCCTT	4688
rs751225786	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568107	CTTCCAGCTGACAGG[A/G]AGCTTAGGAATGAGC	4688
rs751259507	snp	C/T	1.66087e-05	0.00288168	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590410	CTCCCCTAGCAGGGC[C/T]GCCTTAGTGGCCCCC	4688
rs751323633	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568940	CCATCCCCATCATAT[C/T]ATTCCTTTCTAGCCT	4688
rs751325944	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183587922	CCAAGTTCCTTTTTC[A/C]TTAGTGTAGCTTTCA	4688
rs751328813	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183563858	AGGCTATTAAGAAGG[A/T]CCCTAGCTCATGGAC	4688
rs751432737	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574535	ATGTCTGGGCTCAGA[C/T]TTCATGCTCGTGGCC	4688
rs751464263	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183562909	CTTGCTTGACAGTAA[C/T]GGATGGGATGTTTGA	4688
rs751478804	in-del	-/C	1.64743e-05	0.00287	frameshift-variant	NCF2	GRCh38.p7	1:183563241	TAGTTTTTCACCTGG[-/C]CCCAGGCATCCTTCA	4688
rs751502331	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183575482	GTCATACTTTTCCAG[C/G]TCTTGAGTTGGGCTG	4688
rs751537657	snp	A/G	4.94792e-05	0.00497365	intron-variant	NCF2	GRCh38.p7	1:183567001	CTTCTGCAGTGCAGC[A/G]CCACAGAATCAGAAA	4688
rs751617846	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183583692	CGGGCCAGACATATT[A/G]CAAAAGGAGGCTCAA	4688
rs751644304	snp	A/G	3.29538e-05	0.00405904	intron-variant	NCF2	GRCh38.p7	1:183590134	GCACAGAGGAGGCCC[A/G]GAAAGAGGCACCTCC	4688
rs751675908	snp	C/T	5.85817e-05	0.00541179	intron-variant	NCF2	GRCh38.p7	1:183567477	CTGCAACTGCCGAGA[C/T]GACACTGAGCCTGCC	4688
rs751747040	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582588	CTGCACCCAGGACAA[C/T]GGAATCTCAGCAAGC	4688
rs751805957	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183580157	GTAGCAGTGGCTATG[C/T]GGGAAATAAAAGAAG	4688
rs751928437	snp	A/G/T	1.64741e-05	0.00286998	missense	NCF2	GRCh38.p7	1:183565743	GGGCTTTGGAACTAG[A/G/T]AGGAGCTGGGATGTC	4688
rs751980393	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183579669	GCATGAACCCAGGAG[C/G]CAGAGCTTGCAGTGA	4688
rs752028705	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557151	GAGACCCAGAGAGAT[A/G]AATAGTTTGTTCAGA	4688
rs752044043	snp	A/G	3.29451e-05	0.00405851	synonymous-codon	NCF2	GRCh38.p7	1:183586951	CACTGCCAAGTGCTT[A/G]TCTCGGTTAATGCTT	4688
rs752085371	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183571606	GCTTTCTGTGACTGA[A/C]TTGAGCCCTCTTCTC	4688
rs752127520	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183574504	AGACACACTCCATCG[C/T]CTTGTCGATTTTGGA	4688
rs752137410	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589556	GTGAGAAAACATAAC[A/G]AAAAAGATGCGAGAC	4688
rs752217634	snp	A/G	1.64795e-05	0.00287045	synonymous-codon	NCF2	GRCh38.p7	1:183566962	CAGCTCAACTGGTTC[A/G]AGGTAGTTGCAGGGA	4688
rs752232468	snp	A/G	1.64841e-05	0.00287085	intron-variant	NCF2	GRCh38.p7	1:183566893	AAAGGGTGAGAGGAA[A/G]TGGGTCAGGCCTTGG	4688
rs752266227	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183564906	TAGGGTGAAGTGTCA[C/T]GAGTCTGTAACTTTT	4688
rs752384353	snp	A/G/T	8.2364e-05	0.00641686	missense, synonymous-codon	NCF2	GRCh38.p7	1:183590174	CTCTGCTTCAGTCAT[A/G/T]TTCTTCAGGATAGTG	4688
rs752406012	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566519	AAAGTGCTAGGATTA[C/T]AGCCATGAGCAACTG	4688
rs752474014	in-del	-/GAG	4.94246e-05	0.0049709	intron-variant	NCF2	GRCh38.p7	1:183563321	CTGGGTGGGGATAAT[-/GAG]GAGTAAGAATCCAGT	4688
rs752500413	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574365	CTATACCCTAAGATC[A/G]GTGTTACCCAGACTC	4688
rs752527209	in-del	-/C	3.2956e-05	0.00405918	intron-variant	NCF2	GRCh38.p7	1:183577583	CCTGCCCAGGCCAGG[-/C]CCCTGTTCTCCTTAC	4688
rs752593833	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183573606	AGAGGGCACCACCAC[A/G]ACAAGGCTGGCCCGG	4688
rs752642057	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183588277	TGCTCTGTGGAAGAT[-/A]AAAAAAGATAGGGAA	4688
rs752696377	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183586389	CTGTATAAGTGCATA[C/T]GCTACTTACTTATCT	4688
rs752716643	snp	G/T	1.64732e-05	0.0028699	intron-variant	NCF2	GRCh38.p7	1:183574448	ACAAATGAGAATCCA[G/T]TGACATCCTCTCAAC	4688
rs752728286	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183586296	CTGAGATCGAGCCCT[C/T]GCACTCCAGCCTGGG	4688
rs752815840	snp	C/T	1.65614e-05	0.00287757	intron-variant	NCF2	GRCh38.p7	1:183577734	AGGGAGAAAATACAG[C/T]AGTCTAGTGGATGGA	4688
rs752901695	snp	A/G	3.29451e-05	0.00405851	stop-gained	NCF2	GRCh38.p7	1:183586923	AGTAGAGCATCCCTC[A/G]TTGGAAGTAAGCCAC	4688
rs752959739	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183556977	GAACTCCATTAAACA[A/G]GTGAGCTGGAGCTAG	4688
rs752982807	snp	A/G	1.64819e-05	0.00287066	intron-variant	NCF2	GRCh38.p7	1:183560318	CCAATTTCCTGCCAA[A/G]TGAACACTGAACATC	4688
rs752991966	snp	C/T	1.83296e-05	0.00302729	intron-variant	NCF2	GRCh38.p7	1:183567462	TAACTCCACATCTAA[C/T]TGCAACTGCCGAGAT	4688
rs753119745	in-del	-/TTG			intron-variant	NCF2	GRCh38.p7	1:183579872	ATAATTTTTTTACTA[-/TTG]TTTTTGTTGTTTTAT	4688
rs753191763	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582133	CCCATTACACAGGTT[C/T]GCAATAATCTCAGTA	4688
rs753200591	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183581824	AGGCGTCCGCCACCG[C/T]GCCCGGCTAATTTTT	4688
rs753210181	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570329	GCTGCCTGTGTTCCC[A/G]AAGGAAACCCCTGCA	4688
rs753210558	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183560921	TCTTAGCATCAACTC[-/T]TAACAGCAACACTAG	4688
rs753309403	snp	A/C			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555586	AAAACAAACAAGTTT[A/C]TTTGTATATGCCTTA	4688
rs753387368	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183586350	GAAAAAGAAAAAAAA[-/G]TTAACATCTACTGCA	4688
rs753471440	snp	A/G	1.64743e-05	0.00287	synonymous-codon	NCF2	GRCh38.p7	1:183565753	ACTAGGAGGAGCTGG[A/G]ATGTCGGACTGCGGA	4688
rs753524717	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183589444	TAGGATTCGATCCTA[C/G]ATCTTCTCCTTCCAA	4688
rs753556861	snp	C/G	1.65061e-05	0.00287277	missense	NCF2	GRCh38.p7	1:183567343	GCCTCCCCTTCCAGA[C/G]CCCTGCAGAGGATAG	4688
rs753577199	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183588890	CCAAGGCAGGAGGCT[A/G]CAGTCCCTGCTGGCA	4688
rs753644811	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183571938	CATACTCCATTCCTT[G/T]TTATGGCTACGTAGT	4688
rs753682768	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183566428	ATTTTTATTTGTATA[C/G]AGGTGGCATCTCTCT	4688
rs753696208	snp	C/T	0.000115353	0.00759362	intron-variant	NCF2	GRCh38.p7	1:183560310	TAATTTTCCCAATTT[C/T]CTGCCAAGTGAACAC	4688
rs753731815	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584218	CCTGAATTGTACATA[A/G]ACGAATGTGTGTGCT	4688
rs753825493	snp	C/T	1.64732e-05	0.0028699	missense	NCF2	GRCh38.p7	1:183563266	CCTTCATGCTGTCTT[C/T]TGAAAGGGGCACCAG	4688
rs753886533	snp	C/T	0.000131781	0.00811621	intron-variant	NCF2	GRCh38.p7	1:183563959	GTTGATAGCCCAAGC[C/T]ATCCCATCTTCTACC	4688
rs753998475	in-del	-/TGTC	1.65474e-05	0.00287636	intron-variant	NCF2	GRCh38.p7	1:183563619	AAGGGAACTCCTGAG[-/TGTC]TGAGGCTTTCTCTCA	4688
rs754041676	snp	A/G	4.94254e-05	0.00497094	missense	NCF2	GRCh38.p7	1:183577672	CCTCGAAGCTGAATC[A/G]AGGCTTCTTTAAGGT	4688
rs754118806	snp	C/T	6.60044e-05	0.00574438	missense	NCF2	GRCh38.p7	1:183567238	GTGGCCCAGTTATCA[C/T]TGCCCTTCTTCAAGA	4688
rs754192116	snp	C/G	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183569182	TGGGTGGAGGCTCAG[C/G]TGCCTATTGAACATT	4688
rs754212622	snp	A/G			downstream-variant-500B	NCF2	GRCh38.p7	1:183555383	AGCTTCATGAACACC[A/G]CTGCTTTTCATCACT	4688
rs754280232	snp	C/T	1.66363e-05	0.00288407	intron-variant	NCF2	GRCh38.p7	1:183570756	CGAGACCTAGGTCCA[C/T]GGAGAAGGTCAGGAC	4688
rs754301658	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183579523	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	4688
rs754356147	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578521	GGGCGAGCGCCACCA[C/T]GCCCGGCTAATTTTT	4688
rs754369694	snp	C/G	1.65061e-05	0.00287277	intron-variant	NCF2	GRCh38.p7	1:183570847	GCCACGACCTAAAAT[C/G]AAGGACAGGAGGGTG	4688
rs754545169	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	NCF2	GRCh38.p7	1:183565756	AGGAGGAGCTGGGAT[A/G]TCGGACTGCGGAGAG	4688
rs754596658	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183564157	CCCTTTAATTTGTGG[G/T]GCAATTATTAACCTT	4688
rs754618147	snp	A/G/T			intron-variant	NCF2	GRCh38.p7	1:183564701	AATCATCCTAGGTTT[A/G/T]TATGTGATCCTTGAT	4688
rs754695841	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183584986	CTGGATATCTTCTCC[C/G]AATCCCAGGCTCTCT	4688
rs754803247	snp	G/T	1.64811e-05	0.00287059	intron-variant	NCF2	GRCh38.p7	1:183560313	TTTTCCCAATTTCCT[G/T]CCAAGTGAACACTGA	4688
rs754832075	snp	C/T	1.70822e-05	0.00292247	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590441	AAGGTGTTCACTTTC[C/T]GGGCCAGATGAGTAG	4688
rs754874318	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183573519	TATTTGTTGCTATTC[A/G]GCACCCTCTTTTCCC	4688
rs754890421	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183559383	CAGGATAGTTCTGAA[G/T]AGCTGGTTTTTAAGG	4688
rs754891399	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584300	GTTGTAAAAGGGAAA[A/G]GGGTCAAGAACAGAA	4688
rs754896994	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183586168	GGAGAAACCCCATCT[C/G]TACTAAAAATACAAA	4688
rs755115727	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578525	GAGCGCCACCACGCC[C/T]GGCTAATTTTTTATA	4688
rs755128682	snp	C/T	1.6476e-05	0.00287014	intron-variant	NCF2	GRCh38.p7	1:183577585	CTGCCCAGGCCAGGC[C/T]CTGTTCTCCTTACCT	4688
rs755198136	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560568	TGTTCCACCTCAGAT[C/T]GTCAGGCATTAGATT	4688
rs755209791	snp	G/T	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183560191	TCCACTTGGCTGCCT[G/T]TCTTAAGCTGAGGTT	4688
rs755222977	snp	C/G	3.29511e-05	0.00405887	missense	NCF2	GRCh38.p7	1:183577675	CGAAGCTGAATCAAG[C/G]CTTCTTTAAGGTCTT	4688
rs755277258	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576662	AACTGCAAAGCCCCA[C/T]CTTCTCAGACTGTGA	4688
rs755290534	snp	A/C/G	0.000181635	0.0095282	intron-variant	NCF2	GRCh38.p7	1:183567351	TTCCAGAGCCCTGCA[A/C/G]AGGATAGACACAAGA	4688
rs755372753	snp	C/G	0.000164758	0.0090748	intron-variant	NCF2	GRCh38.p7	1:183586855	ACCCCTTGGGTTTCT[C/G]TCTGAAATCCTCCAG	4688
rs755413314	snp	A/G			downstream-variant-500B	NCF2	GRCh38.p7	1:183555393	ACACCGCTGCTTTTC[A/G]TCACTTAAATGTTGG	4688
rs755434573	snp	C/T	1.64882e-05	0.00287121	missense	NCF2	GRCh38.p7	1:183563539	ACTACCGTGTACTTG[C/T]AGTGCACCTTGAGTG	4688
rs755545832	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183575547	ACAATTTACACACAG[A/C]ATCAAATAATCGTTT	4688
rs755614780	snp	A/G	1.68091e-05	0.00289901	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590427	CCTTAGTGGCCCCCA[A/G]GGTGTTCACTTTCTG	4688
rs755672134	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183587845	TAGACATTTACCTGA[A/T]ACTAATAAAAAATAC	4688
rs755689355	snp	C/T	4.94189e-05	0.00497062	missense	NCF2	GRCh38.p7	1:183564013	ATGTTACCTTAGGCT[C/T]TTCTTTTTGTTTCTG	4688
rs755707344	snp	C/T	6.58903e-05	0.00573941	intron-variant	NCF2	GRCh38.p7	1:183573140	CCTTGCTCCACATGG[C/T]CCGGGCCACAGGAGA	4688
rs755742989	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574793	CTATTGAGTTATGTC[A/G]AACACAAACATGGTG	4688
rs755778188	snp	A/C/G	4.94216e-05	0.00497079	missense	NCF2	GRCh38.p7	1:183565746	CTTTGGAACTAGGAG[A/C/G]AGCTGGGATGTCGGA	4688
rs755796920	snp	A/G/T	1.64727e-05	0.00286986	NCF2	1	allele_origin=G(germline)/A(germline)	1:183573229	CCAGCTGAGCCACTT[A/G/T]TCTCTCATTTGGTCG	4688
rs755918616	snp	C/T	1.6477e-05	0.00287024	missense	NCF2	GRCh38.p7	1:183556203	CCCACCTTCCCTTTG[C/T]ACTCCCCTTCCAGCC	4688
rs755949140	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582888	CTGAGACTCTGCTTG[C/T]CTTTTCAGAAATGTG	4688
rs755990384	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183565212	CACTTCCCAAGACAG[A/C]CCTCTCCACACTAGG	4688
rs756008519	snp	C/T	3.29462e-05	0.00405857	missense	NCF2	GRCh38.p7	1:183560159	CTGGTTGGGTAGCCT[C/T]ATAACTGAAGAGTGC	4688
rs756028049	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183588689	ACAATTAAAATGATA[A/C]TGAATAAGAATGCAT	4688
rs756038744	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183584041	AGGTGGATTTAAGAA[A/C]TATTTAAGAGGTCAA	4688
rs756096640	snp	C/T	1.64773e-05	0.00287026	intron-variant	NCF2	GRCh38.p7	1:183560295	TAATAAAGGGCCTGT[C/T]AATTTTCCCAATTTC	4688
rs756141875	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183561987	TCAGTAGAGATGGGG[-/T]TTTCACCATGTTGCC	4688
rs756153547	snp	G/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183590949	CTGCTCTTTCCCAAT[G/T]AATTATTTCTGACTA	4688
rs756157300	snp	C/T	3.29717e-05	0.00406015	synonymous-codon	NCF2	GRCh38.p7	1:183563529	AGTCTTCATGACTAC[C/T]GTGTACTTGTAGTGC	4688
rs756205976	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183589842	GTGCCCAGAAGGAGT[G/T]CTGTGTAGAAGAAAG	4688
rs756293590	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183573937	TCTATTAAAAATACA[A/G]AAATTAGCCAGGCAT	4688
rs756393041	snp	G/T	1.65135e-05	0.00287341	intron-variant	NCF2	GRCh38.p7	1:183567157	AGAGACTGCATTTGC[G/T]GCCAGGATCCCATGC	4688
rs756393096	in-del	-/TAGTGTG	1.64779e-05	0.00287031	frameshift-variant	NCF2	GRCh38.p7	1:183563441	GAGCTCACCTCAGCT[-/TAGTGTG]TTCCAGCCGGAGCTC	4688
rs756420788	snp	C/T	1.64904e-05	0.00287139	intron-variant	NCF2	GRCh38.p7	1:183577566	ATCCAGCCATGATCC[C/T]CTCCTGCCCAGGCCA	4688
rs756453916	snp	C/T	2.45528e-05	0.00350369	intron-variant	NCF2	GRCh38.p7	1:183567501	GCCTGCCTGGGCTCC[C/T]AAGAGGTCTCAGCAA	4688
rs756489228	snp	C/T	1.64751e-05	0.00287007	intron-variant	NCF2	GRCh38.p7	1:183590146	CCCGGAAAGAGGCAC[C/T]TCCACTCACCTTCTC	4688
rs756524438	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566695	CACAGAGGTGGGTGG[A/G]CCCAATGGGACCTAC	4688
rs756529637	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183577483	CTCAAGGCAGAGGAG[A/G]CAAAATGGCTTTTCC	4688
rs756610730	snp	G/T	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183569165	CTCTGGGGTTTTCGG[G/T]CTGGGTGGAGGCTCA	4688
rs756705355	snp	C/T	1.64787e-05	0.00287038	missense	NCF2	GRCh38.p7	1:183563434	CTGCATGGAGCTCAC[C/T]TCAGCTTAGTGTGTT	4688
rs756797744	snp	G/T	1.64749e-05	0.00287005	missense	NCF2	GRCh38.p7	1:183560139	TTCCTGAAACTCCAG[G/T]TCCTCTGGTTGGGTA	4688
rs756851268	snp	C/T	9.90966e-05	0.00703836	synonymous-codon	NCF2	GRCh38.p7	1:183590321	GCTGATGGCCTCCAC[C/T]AGGGACATGATTAGG	4688
rs756864522	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585431	GAGTTCGAGACCAGC[A/G]TGGCCAACATGGTGA	4688
rs756905770	snp	C/G	1.65326e-05	0.00287507	intron-variant	NCF2	GRCh38.p7	1:183570774	AGAAGGTCAGGACTG[C/G]CTTACCTGTGGTTGC	4688
rs756919400	snp	A/T	1.65397e-05	0.00287569	intron-variant	NCF2	GRCh38.p7	1:183570875	GTGTGAGGCTCTGCC[A/T]GCACTGTTTCCATTC	4688
rs756921801	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183581962	GTGAGCCACCTCGCC[C/T]CGCCAACTAAGTGTC	4688
rs756941376	snp	A/G	6.86436e-05	0.00585808	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590411	TCCCCTAGCAGGGCT[A/G]CCTTAGTGGCCCCCA	4688
rs757011233	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183580256	CTACTAAATGCATGC[A/T]GGCCATTCTTTAAGT	4688
rs757058752	snp	C/G	1.64798e-05	0.00287047	intron-variant	NCF2	GRCh38.p7	1:183566902	GAGGAAATGGGTCAG[C/G]CCTTGGCATCACATT	4688
rs757064950	snp	C/T	4.94181e-05	0.00497057	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574544	CTCAGACTTCATGCT[C/T]GTGGCCAATGCTAAC	4688
rs757128560	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575527	CTATTTTACTATTGT[A/G]CTTCACAATTTACAC	4688
rs757139629	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183588978	CATCAGCCCTCAGAA[-/T]GTGTGGTGCTGTTCA	4688
rs757154885	snp	A/G	1.65141e-05	0.00287346	intron-variant	NCF2	GRCh38.p7	1:183567013	AGCACCACAGAATCA[A/G]AAAGGAAAAAATAAA	4688
rs757164414	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183563872	GTCCCTAGCTCATGG[A/G]CTCTGTAAGGTAGCA	4688
rs757201201	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	NCF2	GRCh38.p7	1:183556184	AAAAACTTTGGGGAA[A/G]ATGCCCACCTTCCCT	4688
rs757258719	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574301	GGGCTCTGCCATCCC[A/G]TACTCTAGGCCTCAG	4688
rs757261466	in-del	-/AAAC			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555575	ATGAAAAAAGAAAAC[-/AAAC]AAACAAGTTTATTTG	4688
rs757295495	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	NCF2	GRCh38.p7	1:183569153	TTACCTGAAGATCTC[C/T]GGGGTTTTCGGTCTG	4688
rs757305871	in-del	-/TCT	1.6473e-05	0.00286988	cds-indel	NCF2	GRCh38.p7	1:183564012	AATGTTACCTTAGGC[-/TCT]TCTTTTTGTTTCTGG	4688
rs757423592	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183572486	CATGCACAGCCAAGA[C/T]CTGGATTTAGAAGAA	4688
rs757516561	snp	C/T	1.64784e-05	0.00287035	intron-variant	NCF2	GRCh38.p7	1:183563406	AGGTTCCCACTGTAC[C/T]CCTCACAGCTGCCTG	4688
rs757545051	snp	C/G/T	9.88344e-05	0.00702912	intron-variant	NCF2	GRCh38.p7	1:183574467	CATCCTCTCAACACC[C/G/T]GCATCACCAATACGC	4688
rs757702877	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183558421	TACAAGCACCTACCA[C/G]TATACCCGGCTAATT	4688
rs757752054	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565553	TGGGTGGTGCAGGAA[A/G]GGGGGATTCTGGGGC	4688
rs757849374	snp	A/G	2.02194e-05	0.00317951	intron-variant	NCF2	GRCh38.p7	1:183567481	AACTGCCGAGATGAC[A/G]CTGAGCCTGCCTGGG	4688
rs757916211	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582334	TGGGTGCTTTCTTCA[C/T]ACCCACACTTCAGTG	4688
rs757931282	snp	C/G	1.64789e-05	0.0028704	missense	NCF2	GRCh38.p7	1:183566968	AACTGGTTCAAGGTA[C/G]TTGCAGGGAACAAGC	4688
rs758054999	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566541	GAGCAACTGCAGCTG[A/G]CCTCATTTTCTTTCT	4688
rs758057222	snp	C/T	0.000263631	0.0114781	missense	NCF2	GRCh38.p7	1:183590281	AGTCCTTCTTGTCCG[C/T]TGCCAGCACCCCTTC	4688
rs758100314	snp	C/T	3.29457e-05	0.00405854	intron-variant	NCF2	GRCh38.p7	1:183574455	AGAATCCAGTGACAT[C/T]CTCTCAACACCTGCA	4688
rs758104589	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557587	GTCCTACCCTGACCG[C/T]TAAATTCTGTTTTCT	4688
rs758117639	snp	A/T	1.64727e-05	0.00286986	synonymous-codon	NCF2	GRCh38.p7	1:183569183	GGGTGGAGGCTCAGC[A/T]GCCTATTGAACATTC	4688
rs758132539	in-del	-/TTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561788	CAGGCCTCTTTTTTT[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT	4688
rs758239702	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573266	CTTGCCCACAGGGAT[C/T]ACCACTGGCTCATAT	4688
rs758240915	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560679	CTGCTGATCTGACAG[A/G]AGGCAGAGCTCAGGC	4688
rs758545086	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183569253	GGGAGAGACAACAAA[C/T]GGCTAATGGTAATTT	4688
rs758563917	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183578558	TTAAGTAGAGACCAG[C/G]TTTCACCATGTTGGC	4688
rs758654941	snp	C/T	1.90743e-05	0.00308817	intron-variant	NCF2	GRCh38.p7	1:183567472	TCTAACTGCAACTGC[C/T]GAGATGACACTGAGC	4688
rs758694739	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	NCF2	GRCh38.p7	1:183563294	CAGCTCATTGCTGTC[C/T]CGAGGCCGATAGCTG	4688
rs758694959	snp	A/G/T	3.29469e-05	0.00405864	intron-variant	NCF2	GRCh38.p7	1:183563984	TCTACCACTTGAAAC[A/G/T]GTATGAGGGAAAAAT	4688
rs758760667	snp	A/G			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555660	AGTAATGGTTCAGAA[A/G]CAGGAATATTTGTAC	4688
rs758810345	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183587960	TATCGCTGTTTTAAT[A/T]ATATGATTTAATATG	4688
rs758848635	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570339	TTCCCGAAGGAAACC[C/T]CTGCACATGAGCAGA	4688
rs758862027	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575594	TCTAAAAAATGGCCC[A/G]ACTGAAATAAATTTT	4688
rs758896946	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589447	GATTCGATCCTAGAT[C/T]TTCTCCTTCCAAACT	4688
rs758956466	snp	A/G	0.000115313	0.0075923	synonymous-codon	NCF2	GRCh38.p7	1:183577617	ACAGGCAAACAGCTT[A/G]AACTGGAGCCCCAGG	4688
rs758963978	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557007	GTGATGGGTTAGTAC[A/G]TGTTTGTTAAATATA	4688
rs758993275	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574957	GTGTTGTTTTAGTAT[A/G]AGTTGCTTTAGTAAA	4688
rs759059687	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183577312	CAAGCCAACACACTC[A/G]TGTCCAGCCTCCCTT	4688
rs759074773	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574502	CCAGACACACTCCAT[C/T]GCCTTGTCGATTTTG	4688
rs759089545	snp	A/C			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591680	TAGAGATGGGGTTTC[A/C]CCATGTTGGCCAGGC	4688
rs759102712	snp	A/G	3.29457e-05	0.00405854	intron-variant	NCF2	GRCh38.p7	1:183574441	CTCTGAGACAAATGA[A/G]AATCCAGTGACATCC	4688
rs759173756	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183559813	GCAGTGAGCCGAGAT[G/T]GTGCCACTGCACTCC	4688
rs759177444	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577989	TGCATACAACTGTCA[C/T]CTTTCTGACAACCTG	4688
rs759238583	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576129	TAATGATGTGATTCT[C/T]AGAAGCCAGGGTCAT	4688
rs759257176	snp	C/G	1.73445e-05	0.00294482	intron-variant	NCF2	GRCh38.p7	1:183567446	GGCTCCAGCCTGGCT[C/G]TAACTCCACATCTAA	4688
rs759285400	snp	C/T	1.64757e-05	0.00287012	splice-acceptor-variant, intron-variant	NCF2	GRCh38.p7	1:183574622	AATGTTATATAACAC[C/T]TAGAAAAGTACAGAC	4688
rs759330761	snp	A/G	0.000317044	0.0125866	intron-variant	NCF2	GRCh38.p7	1:183567400	ACATGATGCCATGGC[A/G]CAAATACACTGAACT	4688
rs759398660	in-del	-/T	1.64732e-05	0.0028699	frameshift-variant	NCF2	GRCh38.p7	1:183563259	AGGCATCCTTCATGC[-/T]TGTCTTCTGAAAGGG	4688
rs759409598	snp	C/T	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183587005	GGGTCCAGACATGGC[C/T]ATGATGCAAGGCAGT	4688
rs759471094	snp	G/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183569102	ATCAGCTCAGGCTTG[G/T]CGCTTGGATATTCTA	4688
rs759525280	in-del	-/G	3.29462e-05	0.00405857	intron-variant	NCF2	GRCh38.p7	1:183574450	AAATGAGAATCCAGT[-/G]ACATCCTCTCAACAC	4688
rs759826517	in-del	-/TAATC			intron-variant	NCF2	GRCh38.p7	1:183564460	TAAAGTTTATTAATT[-/TAATC]TAATCTATTAATCAA	4688
rs759940920	snp	C/T	0.00016472	0.00907375	missense	NCF2	GRCh38.p7	1:183560243	CAGCTTTTTCACTTT[C/T]CTTGGGTTCATCTGG	4688
rs759959096	snp	C/T	2.81029e-05	0.00374842	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590400	GTTGGAGCGTCTCCC[C/T]TAGCAGGGCTGCCTT	4688
rs759973985	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570251	AGATCCACTATCATC[C/T]AGTTCATCTGAGCTC	4688
rs759997544	snp	A/G	1.65151e-05	0.00287355	intron-variant	NCF2	GRCh38.p7	1:183570859	AATCAAGGACAGGAG[A/G]GTGTGAGGCTCTGCC	4688
rs760085363	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183573186	GCAATCCCACCTACC[A/G]TCGCCTTGCCTAGGT	4688
rs760087406	snp	A/G	1.64735e-05	0.00286993	intron-variant	NCF2	GRCh38.p7	1:183563960	TTGATAGCCCAAGCT[A/G]TCCCATCTTCTACCA	4688
rs760153375	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570704	AGGCAACTCAGCACA[C/T]ATAGTCTCTCGAATT	4688
rs760169471	snp	A/C	1.64738e-05	0.00286995	missense	NCF2	GRCh38.p7	1:183563249	CACCTGGCCCCAGGC[A/C]TCCTTCATGCTGTCT	4688
rs760234353	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183556903	TACAGAAAAGGGACA[G/T]GCCATTGGTTAAATA	4688
rs760259259	snp	A/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183563315	CCGATAGCTGGGTGG[A/G]GATAATGAGTAAGAA	4688
rs760286541	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183576375	TCTAGAGCCACTTGT[A/C]CCCCAACTTTCTAAT	4688
rs760439163	in-del	-/A	1.64727e-05	0.00286986	frameshift-variant	NCF2	GRCh38.p7	1:183586972	GTTAATGCTTCTGGT[-/A]AAGGCCTGAGGAGAG	4688
rs760440140	in-del	-/GT			intron-variant	NCF2	GRCh38.p7	1:183570557	TGGGGAAGCAGGAGA[-/GT]TAGCTTCAGAGGACT	4688
rs760458285	snp	C/T	8.24776e-05	0.00642122	intron-variant	NCF2	GRCh38.p7	1:183573340	TGAAAATGGGGGTGA[C/T]GATGCTTGTCCTGCC	4688
rs760561718	snp	C/T	1.64969e-05	0.00287196	missense	NCF2	GRCh38.p7	1:183567335	CACGGTGAGCCTCCC[C/T]TTCCAGAGCCCTGCA	4688
rs760718996	snp	C/T	1.67433e-05	0.00289333	intron-variant	NCF2	GRCh38.p7	1:183567409	CATGGCGCAAATACA[C/T]TGAACTTGGAGCCAG	4688
rs760751710	snp	A/C	3.30044e-05	0.00406216	intron-variant	NCF2	GRCh38.p7	1:183570843	AGATGCCACGACCTA[A/C]AATCAAGGACAGGAG	4688
rs760777124	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183570497	AGTTGAGGCTTCAGA[-/G]AGAGGATCAGCAGAT	4688
rs760802211	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183559277	AAGTGATCCTCCTAC[C/G]TCAGCCTCCCTAGTG	4688
rs760850301	snp	A/C	1.64787e-05	0.00287038	intron-variant	NCF2	GRCh38.p7	1:183565662	AAGCAGCCTGGCATG[A/C]TGCTGCACCCAGACC	4688
rs760907985	in-del	-/AATC			intron-variant	NCF2	GRCh38.p7	1:183564474	TTAATCTAATCTATT[-/AATC]AAGCAATCTAATATT	4688
rs760920655	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183584929	TATAAAGTCACAATA[A/C]ATATGTCACACTAAA	4688
rs761119292	snp	G/T	3.30398e-05	0.00406434	intron-variant	NCF2	GRCh38.p7	1:183567184	ATGCCCATCGCACCA[G/T]CCCCTGATCCTCTGC	4688
rs761136334	snp	C/T	0.000148293	0.00860957	synonymous-codon	NCF2	GRCh38.p7	1:183590279	CCAGTCCTTCTTGTC[C/T]GCTGCCAGCACCCCT	4688
rs761193626	snp	C/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591769	GCTGGGATTACAGGA[C/G]TGAGCCACCGTGCCC	4688
rs761201396	in-del	-/TGAG			intron-variant	NCF2	GRCh38.p7	1:183583564	CCAACACTCATTTAT[-/TGAG]TAACTACTATGCTAG	4688
rs761203093	snp	G/T	1.64779e-05	0.00287031	intron-variant	NCF2	GRCh38.p7	1:183560070	AACATGTAAATTTGT[G/T]TCTATAGTCTTGGAG	4688
rs761225814	snp	C/T	1.69292e-05	0.00290935	intron-variant	NCF2	GRCh38.p7	1:183570737	ATGCTTCACAGAAAG[C/T]TCTCGAGACCTAGGT	4688
rs761227257	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183573370	CTCCCTCAGTGAATA[C/G]ATGCAAGAATTCATT	4688
rs761230183	snp	C/T	4.84133e-05	0.00491979	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590392	GAAGACAGGTTGGAG[C/T]GTCTCCCCTAGCAGG	4688
rs761232849	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561671	TTTTAGTACAGATGG[A/G]GTTTCACCATGTTGG	4688
rs761315970	snp	A/G	4.94678e-05	0.00497307	missense	NCF2	GRCh38.p7	1:183567323	ACCCAAATAGCACAC[A/G]GTGAGCCTCCCCTTC	4688
rs761325169	snp	A/G	1.64751e-05	0.00287007	intron-variant	NCF2	GRCh38.p7	1:183560281	TGGTCACCCTGAAAT[A/G]ATAAAGGGCCTGTTA	4688
rs761461157	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556598	GTGCAGTGGCACAAT[C/T]TGGGCTTACTGCAAC	4688
rs761489200	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183569091	CCTTTCTTGCCATCA[A/G]CTCAGGCTTGGCGCT	4688
rs761534825	in-del	-/TC			intron-variant	NCF2	GRCh38.p7	1:183557593	CCCTGACCGCTAAAT[-/TC]TGTTTTCTGTTGAAG	4688
rs761643153	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577074	GGGGACAGATTTATG[C/T]CAAATTATCCTCAGT	4688
rs761693407	snp	A/G	1.65551e-05	0.00287702	intron-variant	NCF2	GRCh38.p7	1:183563624	AACTCCTGAGTGTCT[A/G]AGGCTTTCTCTCAAC	4688
rs761770492	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183583878	GATTGCTTTTTTTAA[A/T]TTTTTTTTTATTTTA	4688
rs761778310	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570176	ATTGCCACAGAGTTC[A/G]TATTTTCCTTAATGT	4688
rs761796267	snp	A/C	3.30251e-05	0.00406343	missense	NCF2	GRCh38.p7	1:183567209	CTCTGCATACCTGCC[A/C]GTTGAACATGACCGT	4688
rs761929939	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566022	TAACCCGCTAAAACG[C/T]CCTTGCCGCTTTAGC	4688
rs761962182	snp	G/T	1.64746e-05	0.00287002	missense	NCF2	GRCh38.p7	1:183590256	CTGAAGGCATCCAGG[G/T]CTCCCTTCCAGTCCT	4688
rs761985515	snp	C/T	4.94964e-05	0.00497451	missense	NCF2	GRCh38.p7	1:183570836	CCACCACAGATGCCA[C/T]GACCTAAAATCAAGG	4688
rs762052296	snp	A/G	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183569228	CGGAAAAGGCAATGA[A/G]GGAAAGCAGGGGAGA	4688
rs762123568	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183576319	GGGAAACATTCCTCC[A/C]ATGGAACTGTACTTT	4688
rs762173491	snp	C/T	1.64779e-05	0.00287031	missense	NCF2	GRCh38.p7	1:183566945	TGCTGAGGGTGGATC[C/T]GCAGCTCAACTGGTT	4688
rs762215620	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183561300	TGTTGTTTGTTGAAC[G/T]TTGGTATATTTTTAT	4688
rs762269733	snp	C/G	3.29712e-05	0.00406011	missense	NCF2	GRCh38.p7	1:183556123	GTGAAACATCCTAGA[C/G]TTCTCTCCGAGTGCT	4688
rs762270172	snp	A/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183574495	CGCTTACCCAGACAC[A/T]CTCCATCGCCTTGTC	4688
rs762271361	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183587331	AGGTGCGGTTGCTCA[-/C]ACCTGTAATCCCAGC	4688
rs762293872	snp	A/C	0.000148274	0.008609	intron-variant	NCF2	GRCh38.p7	1:183590136	ACAGAGGAGGCCCGG[A/C]AAGAGGCACCTCCAC	4688
rs762351295	in-del	-/G	1.64836e-05	0.0028708	intron-variant	NCF2	GRCh38.p7	1:183563174	GGAAATGTAACTTTA[-/G]ATGCCCCTCATTGCA	4688
rs762465566	snp	A/T	1.65157e-05	0.0028736	intron-variant	NCF2	GRCh38.p7	1:183567189	CATCGCACCAGCCCC[A/T]GATCCTCTGCATACC	4688
rs762630439	in-del	-/CCT	1.64727e-05	0.00286986	splice-acceptor-variant	NCF2	GRCh38.p7	1:183569185	GTGGAGGCTCAGCTG[-/CCT]ATTGAACATTCAGGA	4688
rs762714261	snp	A/G	3.29739e-05	0.00406028	synonymous-codon	NCF2	GRCh38.p7	1:183567317	GCACAAACCCAAATA[A/G]CACACGGTGAGCCTC	4688
rs762733492	snp	A/G	4.94222e-05	0.00497078	missense	NCF2	GRCh38.p7	1:183560107	TTACCCTTTGATAAC[A/G]CCAGGATTATATCCC	4688
rs762836805	snp	C/G	1.64784e-05	0.00287035	intron-variant	NCF2	GRCh38.p7	1:183563383	CTTCCCTCCTCCAGG[C/G]CAGCACAAGGTTCCC	4688
rs762845110	snp	A/C/G	4.94184e-05	0.00497063	intron-variant	NCF2	GRCh38.p7	1:183569223	GAAAACGGAAAAGGC[A/C/G]ATGAGGGAAAGCAGG	4688
rs762936258	snp	C/T	3.29641e-05	0.00405968	synonymous-codon	NCF2	GRCh38.p7	1:183563505	CTGGCTGTAGGGGAG[C/T]CCGGGCTGAGTCTTC	4688
rs763012028	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582449	TGCCATAGCTTTTCA[C/T]AAGCTCCAGGCTTGA	4688
rs763140210	snp	C/T	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183586931	ATCCCTCGTTGGAAG[C/T]AAGCCACTGCCAAGT	4688
rs763175896	snp	C/G	1.6571e-05	0.0028784	intron-variant	NCF2	GRCh38.p7	1:183563634	TGTCTGAGGCTTTCT[C/G]TCAACATCCTGGATC	4688
rs763184525	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183557695	TCTCCATATCTACCC[-/A]AAAGGTTGTTTTAGT	4688
rs763196537	snp	G/T	0.000280087	0.0118307	intron-variant	NCF2	GRCh38.p7	1:183590127	AACAAATGCACAGAG[G/T]AGGCCCGGAAAGAGG	4688
rs763317358	snp	C/T	1.64727e-05	0.00286986	splice-donor-variant	NCF2	GRCh38.p7	1:183569141	TTTGAATCTAACTTA[C/T]CTGAAGATCTCTGGG	4688
rs763358790	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183572513	AGAAGTCCAATTTAA[C/G]ACATAGTCTAAACAT	4688
rs763373300	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183573841	ATGCCTGTAATCCCT[-/G]CACTTTGGGAGGCCA	4688
rs763388019	snp	G/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183573199	CCGTCGCCTTGCCTA[G/T]GTAATCCTTCTTGGC	4688
rs763419286	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566653	CTGTAGGCTTTGCTT[C/T]CCAAGTGACTTCTGA	4688
rs763456006	snp	A/G	1.6492e-05	0.00287154	intron-variant	NCF2	GRCh38.p7	1:183566999	CCCTTCTGCAGTGCA[A/G]CACCACAGAATCAGA	4688
rs763538333	snp	A/G	1.64792e-05	0.00287042	intron-variant	NCF2	GRCh38.p7	1:183574642	AAAGTACAGACCGCA[A/G]CATAAAACTTGAGAC	4688
rs763616874	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570688	AGGAGCCCTTACAAT[C/T]AGGCAACTCAGCACA	4688
rs763683515	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183568930	GTCAAGACTCCCATC[A/C]CCATCATATCATTCC	4688
rs763690773	snp	C/T	1.65146e-05	0.0028735	intron-variant	NCF2	GRCh38.p7	1:183567194	CACCAGCCCCTGATC[C/T]TCTGCATACCTGCCC	4688
rs763692318	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183579372	GCTCCGTCACTTACT[A/G]TCTGGTGAGAAACGG	4688
rs763794252	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183575340	CTGGGCATGGTGGCA[G/T]GCACCTGTAATCTCA	4688
rs763800219	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183563706	CAGGGGAGAGGCCAG[C/T]AAGTAACTGGTTTCA	4688
rs763816212	snp	A/C	4.94434e-05	0.00497184	missense	NCF2	GRCh38.p7	1:183590290	TGTCCGCTGCCAGCA[A/C]CCCTTCATTCCAGAG	4688
rs763888116	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183567901	CTGCCGTGGTGCAGT[A/G]TCGGTTCCCTTAAGT	4688
rs763900051	in-del	-/TGGC	3.68263e-05	0.0042909	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590417	GCAGGGCTGCCTTAG[-/TGGC]TGGCCCCCAAGGTGT	4688
rs763929865	snp	C/G/T			utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590517	GCATCAGGAAATGTC[C/G/T]CCACCTTTTGGCAAC	4688
rs763969597	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183569628	GAGTTTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	4688
rs764069114	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587322	ATAATTCCCAGGTGC[A/G]GTTGCTCACACCTGT	4688
rs764142541	snp	A/G/T	3.29457e-05	0.00405854	missense, intron-variant	NCF2	GRCh38.p7	1:183574545	TCAGACTTCATGCTC[A/G/T]TGGCCAATGCTAACT	4688
rs764172732	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183582520	TTTCTTAGTAACCTG[C/T]TTGTTCCCATGCTGC	4688
rs764184085	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570400	GCCCAGGCCCCACAG[A/G]GTTCCCCACTTGCCC	4688
rs764187192	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	NCF2	GRCh38.p7	1:183586945	GTAAGCCACTGCCAA[A/G]TGCTTGTCTCGGTTA	4688
rs764216316	in-del	-/CAAAA			intron-variant	NCF2	GRCh38.p7	1:183574088	AGCGAGACTCCATCT[-/CAAAA]CAAAACAAAACAAAA	4688
rs764311226	snp	A/G	7.6438e-05	0.00618168	intron-variant	NCF2	GRCh38.p7	1:183567473	CTAACTGCAACTGCC[A/G]AGATGACACTGAGCC	4688
rs764314608	snp	C/G	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183573220	CCTTCTTGGCCAGCT[C/G]AGCCACTTGTCTCTC	4688
rs764328286	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564907	AGGGTGAAGTGTCAC[A/G]AGTCTGTAACTTTTC	4688
rs764390490	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183583579	TGAGTAACTACTATG[A/C]TAGATACTGAAATAC	4688
rs764404690	snp	C/T	3.29473e-05	0.00405864	missense	NCF2	GRCh38.p7	1:183565740	CAGGGGCTTTGGAAC[C/T]AGGAGGAGCTGGGAT	4688
rs764405660	snp	A/G	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183569148	CTAACTTACCTGAAG[A/G]TCTCTGGGGTTTTCG	4688
rs764435858	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183558303	GACTGAGTCTCACTC[C/T]GTAACCCAGGCTGGA	4688
rs764497575	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589530	GCTTAACTCCATACT[A/G]TGGTATTTGAGTGAG	4688
rs764587406	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590665	CCCAAAATGCTTCTG[C/T]TCTGTCACCCAGCTC	4688
rs764627778	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183571536	AAGAAAATGCTGTAC[A/C]CATTAAGCAGTGTGT	4688
rs764637284	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566464	GCCCAGGCTGGTCTC[A/G]AACTCCTGAGTTCAA	4688
rs764663614	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183557013	GGTTAGTACATGTTT[G/T]TTAAATATAAATATT	4688
rs764805270	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183567824	CAGGATAGAGAGACC[A/G]TGAGCAGGGTAGGTG	4688
rs764838698	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578059	AGCTCCAAGCAGAGC[C/T]AGCACCTGCCCCCTG	4688
rs764862093	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183573550	AGAGGAACTGCTCCT[C/G]TCCCACTCTGTGTGC	4688
rs764883778	snp	A/T	3.29777e-05	0.00406051	intron-variant	NCF2	GRCh38.p7	1:183566877	CCAGGGAGAGATCCC[A/T]AAAGGGTGAGAGGAA	4688
rs764941884	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183583734	GACGCTGCCTTAGTG[G/T]TTGGGCATGGCTGGG	4688
rs764967944	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183574304	CTCTGCCATCCCATA[C/T]TCTAGGCCTCAGCTT	4688
rs765026266	snp	A/T	1.75148e-05	0.00295924	intron-variant	NCF2	GRCh38.p7	1:183567451	CAGCCTGGCTCTAAC[A/T]CCACATCTAACTGCA	4688
rs765110090	snp	C/T	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183563284	AAAGGGGCACCAGCT[C/T]ATTGCTGTCCCGAGG	4688
rs765235671	snp	G/T	1.64738e-05	0.00286995	missense	NCF2	GRCh38.p7	1:183565719	CTGGTGACAGCTGGG[G/T]TCTTCCAGGGGCTTT	4688
rs765356034	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183576457	GTTGTCACATTGGGT[A/G]GGGAGTGGTGGTGGC	4688
rs765400770	snp	A/G	1.64923e-05	0.00287156	missense	NCF2	GRCh38.p7	1:183563543	CCGTGTACTTGTAGT[A/G]CACCTTGAGTGTGTA	4688
rs765454120	snp	C/G	1.64735e-05	0.00286993	missense	NCF2	GRCh38.p7	1:183560264	GTTCATCTGGAAAGC[C/G]TTGGTCACCCTGAAA	4688
rs765461476	snp	G/T	1.64762e-05	0.00287016	missense	NCF2	GRCh38.p7	1:183577681	TGAATCAAGGCTTCT[G/T]TAAGGTCTTTGATAG	4688
rs765474320	snp	A/G	3.31598e-05	0.00407171	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590407	CGTCTCCCCTAGCAG[A/G]GCTGCCTTAGTGGCC	4688
rs765539224	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575326	AATACAAAAATTAGC[C/T]GGGCATGGTGGCAGG	4688
rs765562133	snp	C/G	1.65239e-05	0.00287431	intron-variant	NCF2	GRCh38.p7	1:183570866	GACAGGAGGGTGTGA[C/G]GCTCTGCCAGCACTG	4688
rs765572643	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183585421	ACAAGGTCAGGAGTT[C/T]GAGACCAGCGTGGCC	4688
rs765601778	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183562459	CAGGGAGTCTCATCC[C/G]CAGTGGCTGTATTTC	4688
rs765634116	in-del	-/TTTTAA			intron-variant	NCF2	GRCh38.p7	1:183558244	CCCCATTAACTTTTT[-/TTTTAA]TTTTAATTTTTTTGT	4688
rs765635816	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556905	CAGAAAAGGGACATG[C/T]CATTGGTTAAATATA	4688
rs765699858	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183569214	AGGAGAAGTGAAAAC[A/G]GAAAAGGCAATGAGG	4688
rs765720927	snp	A/T	4.94205e-05	0.0049707	intron-variant	NCF2	GRCh38.p7	1:183563961	TGATAGCCCAAGCTA[A/T]CCCATCTTCTACCAC	4688
rs765749523	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183563927	CTCTTCCTATAATCC[A/G]GACAGACATGTCTGT	4688
rs765762727	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183573187	CAATCCCACCTACCG[C/T]CGCCTTGCCTAGGTA	4688
rs765799962	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576417	GCTGTCATTGGCTTA[C/T]TAGCAATGTCTGGAG	4688
rs765806399	snp	C/T	1.64735e-05	0.00286993	missense	NCF2	GRCh38.p7	1:183563262	GCATCCTTCATGCTG[C/T]CTTCTGAAAGGGGCA	4688
rs765868844	in-del	-/AG	3.29506e-05	0.00405884	frameshift-variant	NCF2	GRCh38.p7	1:183563214	GTGTTCTCACACCAC[-/AG]AGTCAGGCAGTAGTT	4688
rs765882551	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565368	CCATGCCCCTCAGAG[A/G]TAAGCAGGTATAGTT	4688
rs765922787	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183577195	GCAGGTCCTGCACGG[A/G]CAATGAACTCATGAT	4688
rs765993517	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589337	TCTCACTTAATTTTC[A/G]TGATATTTAGAAACT	4688
rs766060302	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560793	AAAAGGTCTGCAAAA[C/T]CATATACAGTCTTAA	4688
rs766146068	snp	A/G	1.64751e-05	0.00287007	missense	NCF2	GRCh38.p7	1:183577669	TTCCCTCGAAGCTGA[A/G]TCAAGGCTTCTTTAA	4688
rs766212498	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571855	ATTGTACAACATGTG[A/G]CCTTTCGTATCTGGC	4688
rs766217153	snp	A/G	1.6904e-05	0.00290719	intron-variant	NCF2	GRCh38.p7	1:183567425	TGAACTTGGAGCCAG[A/G]GACTTGGCTCCAGCC	4688
rs766232480	snp	A/G	1.65051e-05	0.00287267	synonymous-codon	NCF2	GRCh38.p7	1:183567341	GAGCCTCCCCTTCCA[A/G]AGCCCTGCAGAGGAT	4688
rs766259413	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566425	ATTATTTTTATTTGT[A/G]TAGAGGTGGCATCTC	4688
rs766294215	snp	C/T	4.94328e-05	0.00497131	intron-variant	NCF2	GRCh38.p7	1:183560302	GGGCCTGTTAATTTT[C/T]CCAATTTCCTGCCAA	4688
rs766295237	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584953	CACTAAATATGGGGG[A/G]AAGAGAGAGCTAAAT	4688
rs766392347	snp	A/C	1.6504e-05	0.00287258	intron-variant	NCF2	GRCh38.p7	1:183570845	ATGCCACGACCTAAA[A/C]TCAAGGACAGGAGGG	4688
rs766403210	snp	A/G	1.64741e-05	0.00286998	intron-variant	NCF2	GRCh38.p7	1:183563956	GTGGTTGATAGCCCA[A/G]GCTATCCCATCTTCT	4688
rs766479509	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560473	CCAACCTTTTTGGCA[C/T]GAGGGACCAGTTTCA	4688
rs766511565	snp	C/T	1.64909e-05	0.00287144	intron-variant	NCF2	GRCh38.p7	1:183577568	CCAGCCATGATCCCC[C/T]CCTGCCCAGGCCAGG	4688
rs766551538	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183574133	GCTGTTATGTGCCTA[A/G]CACTGTGCCAGGCTG	4688
rs766743909	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183586266	TTGAGCCTGGGAGGC[A/G]GAGGCTGCGGTGAGC	4688
rs766745748	snp	A/G	1.64727e-05	0.00286986	stop-gained, intron-variant	NCF2	GRCh38.p7	1:183573244	GTCTCTCATTTGGTC[A/G]AAACAGCTTGCCCAC	4688
rs766761572	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183579509	AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCGA	4688
rs766870290	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183587697	ATCACCAACAGAAAT[A/C]TTAGAAGAAAAGAAA	4688
rs766870991	snp	A/C	1.68094e-05	0.00289904	intron-variant	NCF2	GRCh38.p7	1:183570743	CACAGAAAGCTCTCG[A/C]GACCTAGGTCCATGG	4688
rs766871548	snp	C/T	1.64751e-05	0.00287007	intron-variant	NCF2	GRCh38.p7	1:183560089	ATAGTCTTGGAGTAG[C/T]ACTTACCCTTTGATA	4688
rs766880844	snp	C/T	1.64743e-05	0.00287	synonymous-codon	NCF2	GRCh38.p7	1:183560145	AAACTCCAGGTCCTC[C/T]GGTTGGGTAGCCTCA	4688
rs766952838	snp	A/G	1.64914e-05	0.00287149	synonymous-codon	NCF2	GRCh38.p7	1:183567324	CCCAAATAGCACACG[A/G]TGAGCCTCCCCTTCC	4688
rs767086162	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183590027	TAAATCAGGCTGTCT[A/G]GGGGTGGAGCTTGGG	4688
rs767108403	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556717	TGTATTTATTAGAGA[C/T]AGGATCTCGCCATGT	4688
rs767119882	in-del	-/AAAC			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555571	CATAATGAAAAAAGA[-/AAAC]AAACAAACAAGTTTA	4688
rs767143237	in-del	-/TACT			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555672	AAACAGGAATATTTG[-/TACT]TACTTACTCCTTGGG	4688
rs767192295	snp	C/T	3.9718e-05	0.00445617	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590421	GGGCTGCCTTAGTGG[C/T]CCCCAAGGTGTTCAC	4688
rs767202963	snp	C/T	1.65811e-05	0.00287929	intron-variant	NCF2	GRCh38.p7	1:183570886	TGCCAGCACTGTTTC[C/T]ATTCTTCTGGGTCTC	4688
rs767231283	snp	A/G			downstream-variant-500B	NCF2	GRCh38.p7	1:183555237	GCTGTGTAGTAGGCT[A/G]TACCATCTAGTCTTG	4688
rs767296397	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565091	GGGAAGGGACATCCC[A/G]AGTGATTCTGATGAT	4688
rs767310465	in-del	-/ATA	1.64741e-05	0.00286998	intron-variant	NCF2	GRCh38.p7	1:183563317	GATAGCTGGGTGGGG[-/ATA]ATGAGTAAGAATCCA	4688
rs767435337	in-del	-/ACGCTTAC	1.6473e-05	0.00286988	splice-donor-variant, intron-variant	NCF2	GRCh38.p7	1:183574479	ACCTGCATCACCAAT[-/ACGCTTAC]CCAGACACACTCCAT	4688
rs767437169	snp	A/G	4.95372e-05	0.00497656	synonymous-codon	NCF2	GRCh38.p7	1:183567210	TCTGCATACCTGCCC[A/G]TTGAACATGACCGTG	4688
rs767454881	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183556438	CATGATAATGAGCAA[A/C]ATGAAGAAGGATAAA	4688
rs767530948	snp	A/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183569237	CAATGAGGGAAAGCA[A/G]GGGAGAGACAACAAA	4688
rs767533151	snp	A/T	3.29516e-05	0.00405891	missense	NCF2	GRCh38.p7	1:183590262	GCATCCAGGGCTCCC[A/T]TCCAGTCCTTCTTGT	4688
rs767622954	snp	G/T	1.64822e-05	0.00287068	missense	NCF2	GRCh38.p7	1:183563509	CTGTAGGGGAGCCCG[G/T]GCTGAGTCTTCATGA	4688
rs767748338	snp	A/G	1.64792e-05	0.00287042	intron-variant	NCF2	GRCh38.p7	1:183563421	CCCTCACAGCTGCCT[A/G]CATGGAGCTCACCTC	4688
rs767857697	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591728	TGACCTCAGGTGATT[C/T]GGCCTCCTCGGCCTC	4688
rs767932699	snp	A/T	0.000263813	0.011482	intron-variant	NCF2	GRCh38.p7	1:183566873	CCCTCCAGGGAGAGA[A/T]CCCTAAAGGGTGAGA	4688
rs767966868	snp	A/G			upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590816	GCCTAGGCAGATAGG[A/G]GCAGGTCCCTGGTGA	4688
rs768016299	snp	C/G	1.64754e-05	0.00287009	intron-variant	NCF2	GRCh38.p7	1:183590139	GAGGAGGCCCGGAAA[C/G]AGGCACCTCCACTCA	4688
rs768016663	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183578182	GGGGCCCCTTCTTAT[A/G]GCTGCCACCATCACC	4688
rs768029053	snp	A/G	1.64779e-05	0.00287031	missense	NCF2	GRCh38.p7	1:183566946	GCTGAGGGTGGATCC[A/G]CAGCTCAACTGGTTC	4688
rs768054621	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183583173	TTCTCCTGCCTCAGC[C/G]TCCCAAGTAGCTGGG	4688
rs768181039	snp	A/C/T	8.24442e-05	0.00641998	missense	NCF2	GRCh38.p7	1:183567322	AACCCAAATAGCACA[A/C/T]GGTGAGCCTCCCCTT	4688
rs768193963	snp	C/T	3.29495e-05	0.00405877	missense	NCF2	GRCh38.p7	1:183577658	CTATCAGCTGGTTCC[C/T]TCGAAGCTGAATCAA	4688
rs768221820	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183558341	GGCACAATCTCAGCT[-/C]ACTGCAACCTCCTCC	4688
rs768273338	snp	A/G	1.68369e-05	0.0029014	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590346	ATTAGGTAGAAACTA[A/G]GAGGCCAAGAGAGCT	4688
rs768283815	snp	A/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183586873	TGAAATCCTCCAGTT[A/G]GTGCAACATTGAACC	4688
rs768284654	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183569599	TTAATTTAAAAAAAA[A/T]TTTTTTTGAGATGGA	4688
rs768437157	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589106	TTGACTTGTCAAGCT[A/G]TGTGAGAACATTTCA	4688
rs768451445	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183590083	CAGAGGTTAGGTTTC[C/T]GAAATGCAATGGGGT	4688
rs768549092	snp	C/G	1.64773e-05	0.00287026	missense	NCF2	GRCh38.p7	1:183566929	CATTACCTGGGGCTG[C/G]TGCTGAGGGTGGATC	4688
rs768602664	snp	A/T	1.64942e-05	0.00287173	missense	NCF2	GRCh38.p7	1:183570820	GAGAAACTGTCTTGA[A/T]CCACCACAGATGCCA	4688
rs768633696	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183580887	AGGAGGGTGAGGCAG[G/T]AGAATCACTTGAACC	4688
rs768663267	in-del	-/TGAATG			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555795	TGTTTACAGTGTGAA[-/TGAATG]CACAGCTGGCTAGCT	4688
rs768694816	snp	A/G	1.65312e-05	0.00287495	intron-variant	NCF2	GRCh38.p7	1:183563600	CCTGAGTGGGGAGGA[A/G]ACAAAGGGAACTCCT	4688
rs768748386	snp	C/T	3.29886e-05	0.00406118	synonymous-codon	NCF2	GRCh38.p7	1:183556118	AGTTTGTGAAACATC[C/T]TAGACTTCTCTCCGA	4688
rs768778355	snp	A/G	3.29473e-05	0.00405864	intron-variant	NCF2	GRCh38.p7	1:183564047	TGAATGGAAAAAGTA[A/G]GGAGTAAAACAAAAG	4688
rs768786785	snp	C/G	1.64738e-05	0.00286995	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574592	CCATTCCTCCTTCTT[C/G]GCATACATGAAAGCA	4688
rs768800076	snp	C/T	0.000231191	0.010749	intron-variant	NCF2	GRCh38.p7	1:183567170	GCTGCCAGGATCCCA[C/T]GCCCATCGCACCAGC	4688
rs768809741	in-del	-/AG			utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590575	AAAGGAAAGAAGCAG[-/AG]AGAGAGAGGGCGAGT	4688
rs768839146	snp	A/C	1.64803e-05	0.00287052	intron-variant	NCF2	GRCh38.p7	1:183566903	AGGAAATGGGTCAGG[A/C]CTTGGCATCACATTA	4688
rs768893403	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565946	ACGAAGGAAATGTTG[A/G]CCAAAAGAGGAGGTG	4688
rs768896227	snp	C/G	3.29796e-05	0.00406063	splice-acceptor-variant	NCF2	GRCh38.p7	1:183556231	GCCATTCTTCATTCA[C/G]TGATAAAAGGAAAAG	4688
rs768995810	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183572571	TCAGCCCACTAAAAC[A/G]TGAACTACAAGGAGC	4688
rs769211195	snp	A/C/G	3.30465e-05	0.00406477	intron-variant	NCF2	GRCh38.p7	1:183563592	CTTCACTTCCTGAGT[A/C/G]GGGAGGAAACAAAGG	4688
rs769245897	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183584685	TTGAGATTTAAGATC[G/T]GCTGAAGGATTTGTT	4688
rs769269175	snp	C/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574490	CAATACGCTTACCCA[C/G]ACACACTCCATCGCC	4688
rs769429861	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183567087	TGGGGAAGGGATGAC[A/G]AACAGACAAAAGAAC	4688
rs769511127	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183577229	GGATTTGCTAGCAAA[A/T]TGCTGAACAAATAGC	4688
rs769516135	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183590084	AGAGGTTAGGTTTCC[A/G]AAATGCAATGGGGTT	4688
rs769538131	in-del	-/T	1.73445e-05	0.00294482	intron-variant	NCF2	GRCh38.p7	1:183567446	GCTCCAGCCTGGCTC[-/T]TAACTCCACATCTAA	4688
rs769568203	in-del	-/GAAGA	9.95685e-05	0.00705509	intron-variant	NCF2	GRCh38.p7	1:183556275	CTAAAACCACTGTAG[-/GAAGA]TTACCCTGTCTGGCT	4688
rs769609589	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183569484	GTGTCACAAGAATGC[C/T]TTGACCTTGAGCTCT	4688
rs769655977	snp	A/G	0.000164758	0.0090748	intron-variant	NCF2	GRCh38.p7	1:183587026	GCAAGGCAGTGAGGA[A/G]GTGTGAGATGAGCCA	4688
rs769656639	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587191	GGTGTGCATTCCTTG[C/T]ATTGTCATTCCAGTT	4688
rs769704327	snp	C/T	1.64735e-05	0.00286993	missense, intron-variant	NCF2	GRCh38.p7	1:183573286	CTGGCTCATATAGCT[C/T]CTGCTTCTGTAACAC	4688
rs769744791	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	NCF2	GRCh38.p7	1:183590234	GGAGTGGGGGTCCTG[A/G]ACGGCACTGAAGGCA	4688
rs769779675	snp	A/G	8.23839e-05	0.00641757	synonymous-codon	NCF2	GRCh38.p7	1:183556157	CAAATCTGTAGTTGC[A/G]CAGTCTTCAACAAAA	4688
rs769832894	snp	A/G	4.94181e-05	0.00497057	intron-variant	NCF2	GRCh38.p7	1:183569217	AGAAGTGAAAACGGA[A/G]AAGGCAATGAGGGAA	4688
rs769837205	snp	C/G	3.29598e-05	0.00405941	missense	NCF2	GRCh38.p7	1:183563490	CACCATGTCCCGGAC[C/G]TGGCTGTAGGGGAGC	4688
rs769923458	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183576818	CTGAGAAACTAAAGC[A/C]AGGGGACTTTTGTCA	4688
rs769945870	snp	C/T	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183574474	TCAACACCTGCATCA[C/T]CAATACGCTTACCCA	4688
rs770006318	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183564553	GGGGGTACATGATCA[C/G]AGAAGGCCACTGATC	4688
rs770071182	snp	C/G	1.65504e-05	0.00287662	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556104	TTCTTCAGCTTTGTA[C/G]TTTGTGAAACATCCT	4688
rs770127634	snp	A/G	1.66565e-05	0.00288583	intron-variant	NCF2	GRCh38.p7	1:183567395	CCCTCACATGATGCC[A/G]TGGCGCAAATACACT	4688
rs770142716	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183583539	TATATTTTGCTCACT[G/T]TTATTTAATCCAACA	4688
rs770216923	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589609	GACATCACTAGTCAA[C/T]CACAGTACAATTTCC	4688
rs770284550	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	NCF2	GRCh38.p7	1:183590222	GAAGCAAATCCGGGA[A/G]TGGGGGTCCTGGACG	4688
rs770347930	in-del	-/A	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183573159	GGCCACAGGAGACTC[-/A]GGGGAAGCTGAGCAA	4688
rs770372216	snp	C/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183569198	TGCCTATTGAACATT[C/T]AGGAGAAGTGAAAAC	4688
rs770383642	snp	C/T	1.64955e-05	0.00287184	intron-variant	NCF2	GRCh38.p7	1:183565797	GAAGGCAACAGGGAG[C/T]GACGGTCAGAACCTT	4688
rs770408450	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183573752	AGCCTTATTCACAAA[C/T]ATGCTTGAACGATAA	4688
rs770409907	snp	A/G	4.49751e-05	0.00474189	intron-variant	NCF2	GRCh38.p7	1:183567548	TGCTCATAACCATAT[A/G]TGCAGAGGGGCAAGA	4688
rs770440400	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183559685	TCAACATGGCAAAAC[C/T]CCATCTCTACTAAAT	4688
rs770447480	snp	C/G	1.64754e-05	0.00287009	intron-variant	NCF2	GRCh38.p7	1:183563322	CTGGGTGGGGATAAT[C/G]AGTAAGAATCCAGTC	4688
rs770486258	snp	A/G			synonymous-codon	NCF2	GRCh38.p7	1:183577701	GTCTTTGATAGCCAA[A/G]TCATATCTGCAGGAC	4688
rs770533400	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183572404	GGCCAGCCTGGTCTT[A/G]AACTCCTGACCTCGT	4688
rs770537584	snp	C/T	1.64787e-05	0.00287038	missense	NCF2	GRCh38.p7	1:183563462	GTTCCAGCCGGAGCT[C/T]CAGTTTCTTAGACAC	4688
rs770674754	snp	C/G	1.64727e-05	0.00286986	missense	NCF2	GRCh38.p7	1:183586915	TGTCTGGTAGTAGAG[C/G]ATCCCTCGTTGGAAG	4688
rs770858291	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575969	GTTGGCTTCTCCAGC[C/T]CACTCCTGACCTTGT	4688
rs770972754	snp	G/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183556053	GTATACAGCAGAAGG[G/T]TGCTAAATCTTACAA	4688
rs771034067	snp	A/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183573173	CAGGGGAAGCTGAGC[A/T]ATCCCACCTACCGTC	4688
rs771119414	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183587136	TCTCACGGTGCACCC[C/G]ACTTCGCTCTCACAT	4688
rs771120104	snp	A/C/T	3.29458e-05	0.00405857	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573281	CACCACTGGCTCATA[A/C/T]AGCTTCTGCTTCTGT	4688
rs771126735	snp	C/T	1.64784e-05	0.00287035	splice-acceptor-variant	NCF2	GRCh38.p7	1:183565781	GGAGAGCTTTCCTCC[C/T]GAAGGCAACAGGGAG	4688
rs771164166	snp	C/G	1.6477e-05	0.00287024	intron-variant	NCF2	GRCh38.p7	1:183565674	ATGCTGCTGCACCCA[C/G]ACCTAGGCTGTGGCT	4688
rs771262057	snp	A/G	1.64735e-05	0.00286993	missense	NCF2	GRCh38.p7	1:183577633	AACTGGAGCCCCAGG[A/G]TCTTATAGTCTATCA	4688
rs771293387	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183583141	CACTGCAACATCTGC[C/T]TCCCAGGTCCAAGCT	4688
rs771296779	snp	A/G			missense	NCF2	GRCh38.p7	1:183566942	TGCTGCTGAGGGTGG[A/G]TCCGCAGCTCAACTG	4688
rs771349846	snp	A/G	3.29696e-05	0.00406001	synonymous-codon	NCF2	GRCh38.p7	1:183567282	CCCTGGCATGACCTG[A/G]AGCTCTTCTTTTGTC	4688
rs771356784	snp	C/T	1.65187e-05	0.00287386	intron-variant	NCF2	GRCh38.p7	1:183567185	TGCCCATCGCACCAG[C/T]CCCTGATCCTCTGCA	4688
rs771465757	in-del	-/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555724	TTGTAAGATGCTAGG[-/T]TTTTTTTTTATTGTG	4688
rs771477568	in-del	-/AGAG			utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590573	GAAAAGGAAAGAAGC[-/AGAG]AGAGAGAGGGCGAGT	4688
rs771483075	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589813	TGTAAAGCGCTGGGA[C/T]AGATAGAGATTCTGT	4688
rs771528312	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183575772	TCATGTAGCGAAGAA[A/C]TGAGGCCTCCTGCCA	4688
rs771532464	snp	C/T	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183560225	TTGTCTGGTTATTAG[C/T]ATCAGCTTTTTCACT	4688
rs771632691	snp	A/G	1.64849e-05	0.00287092	intron-variant	NCF2	GRCh38.p7	1:183563168	CTCAGTGGAAATGTA[A/G]CTTTAGATGCCCCTC	4688
rs771688022	snp	G/T	3.54893e-05	0.00421229	intron-variant	NCF2	GRCh38.p7	1:183567534	AACTGGTGTACACCT[G/T]CTCATAACCATATAT	4688
rs771700890	snp	A/G	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183573161	CCACAGGAGACTCAG[A/G]GGAAGCTGAGCAATC	4688
rs771769576	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557762	CTCCAGACAATTGAG[C/T]TGGTTGGTTGATTTA	4688
rs772105102	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568501	TTTTTGGGTGGGAGG[A/G]CCAGGCTTGCTTCAT	4688
rs772178602	snp	A/G	1.77341e-05	0.00297771	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590359	TAGGAGGCCAAGAGA[A/G]CTGCCAGGAGACAGA	4688
rs772204296	snp	G/T	1.64732e-05	0.0028699	missense	NCF2	GRCh38.p7	1:183560205	TTTCTTAAGCTGAGG[G/T]TCTGTTGTCTGGTTA	4688
rs772322729	snp	A/G	1.64988e-05	0.00287213	synonymous-codon	NCF2	GRCh38.p7	1:183570837	CACCACAGATGCCAC[A/G]ACCTAAAATCAAGGA	4688
rs772348707	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592868	TGCTTACTCTTCTCC[C/T]GCTATGCCTTCATTC	4688
rs772503928	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574496	GCTTACCCAGACACA[C/T]TCCATCGCCTTGTCG	4688
rs772517639	snp	C/T	1.64795e-05	0.00287045	intron-variant	NCF2	GRCh38.p7	1:183560057	CCTTGTTTCTGCTAA[C/T]ATGTAAATTTGTTTC	4688
rs772542216	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557837	CCACTGAGTTACCAT[C/T]CTCTCTTGTTGGAAC	4688
rs772569356	in-del	-/T	1.6477e-05	0.00287024	frameshift-variant	NCF2	GRCh38.p7	1:183556174	GTCTTCAACAAAAAC[-/T]TTTGGGGAAAATGCC	4688
rs772598020	snp	C/T	1.64754e-05	0.00287009	missense, intron-variant	NCF2	GRCh38.p7	1:183574614	ATGAAAGCAATGTTA[C/T]ATAACACCTAGAAAA	4688
rs772674498	snp	A/G	5.02105e-05	0.00501026	intron-variant	NCF2	GRCh38.p7	1:183567408	CCATGGCGCAAATAC[A/G]CTGAACTTGGAGCCA	4688
rs772695675	in-del	-/A	4.95692e-05	0.00497816	intron-variant	NCF2	GRCh38.p7	1:183567018	ACAGAATCAGAAAGG[-/A]AAAAAATAAAGATGT	4688
rs772766707	in-del	-/A	5.73378e-05	0.00535403	intron-variant	NCF2	GRCh38.p7	1:183567518	AGAGGTCTCAGCAAG[-/A]AACTGGTGTACACCT	4688
rs772770694	snp	C/G	3.58545e-05	0.00423391	intron-variant	NCF2	GRCh38.p7	1:183567535	ACTGGTGTACACCTG[C/G]TCATAACCATATATG	4688
rs772775720	snp	A/G	1.64917e-05	0.00287151	missense	NCF2	GRCh38.p7	1:183567262	TTCAAGACAAAGACA[A/G]TGTTCCCTGGCATGA	4688
rs772793502	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183571010	GATTTCAGCAACTGA[A/C]GAAACGAGCATTCAC	4688
rs772796708	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183559530	GGGAATGAGAATCCA[C/T]GGTTTCCAAAGCATA	4688
rs772821326	in-del	-/TACCCTGTCTGG	9.98336e-05	0.00706448	intron-variant	NCF2	GRCh38.p7	1:183556281	CCACTGTAGGAAGAT[-/TACCCTGTCTGG]CTATTCCACACAGAA	4688
rs772926959	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183566141	TTCCACTTCTCATTT[G/T]CAAGGCATTTGAAGC	4688
rs773006569	in-del	-/AAAAAAAAAA			intron-variant	NCF2	GRCh38.p7	1:183579739	GTGAGACTCTGTCTC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	4688
rs773016794	snp	C/G/T	1.65165e-05	0.00287367	intron-variant	NCF2	GRCh38.p7	1:183567181	CCCATGCCCATCGCA[C/G/T]CAGCCCCTGATCCTC	4688
rs773024248	snp	C/G	1.64795e-05	0.00287045	intron-variant	NCF2	GRCh38.p7	1:183565654	AACTCAGGAAGCAGC[C/G]TGGCATGCTGCTGCA	4688
rs773087261	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591265	GATGGAGAAAAAATC[C/T]TGTGTCACTGGGCCT	4688
rs773113012	in-del	-/ACG			intron-variant	NCF2	GRCh38.p7	1:183573604	GTAGAGGGCACCACC[-/ACG]ACAAGGCTGGCCCGG	4688
rs773131016	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	NCF2	GRCh38.p7	1:183577665	CTGGTTCCCTCGAAG[C/T]TGAATCAAGGCTTCT	4688
rs773175637	snp	A/C	1.6477e-05	0.00287024	missense	NCF2	GRCh38.p7	1:183590269	GGGCTCCCTTCCAGT[A/C]CTTCTTGTCCGCTGC	4688
rs773198494	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577144	ATGGATAGTAAAGAG[C/T]GTGGTCTATAAACTT	4688
rs773234737	snp	C/G	1.6501e-05	0.00287232	splice-acceptor-variant	NCF2	GRCh38.p7	1:183570840	CACAGATGCCACGAC[C/G]TAAAATCAAGGACAG	4688
rs773251896	snp	C/G	1.97603e-05	0.00314321	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590375	CTGCCAGGAGACAGA[C/G]AGAAGACAGGTTGGA	4688
rs773324821	snp	C/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183563954	CTGTGGTTGATAGCC[C/G]AAGCTATCCCATCTT	4688
rs773422870	snp	A/G	1.64754e-05	0.00287009	missense, intron-variant	NCF2	GRCh38.p7	1:183574615	TGAAAGCAATGTTAT[A/G]TAACACCTAGAAAAG	4688
rs773499272	snp	C/G	9.88321e-05	0.00702896	intron-variant	NCF2	GRCh38.p7	1:183573162	CACAGGAGACTCAGG[C/G]GAAGCTGAGCAATCC	4688
rs773499891	snp	G/T	0.000164718	0.00907368	intron-variant	NCF2	GRCh38.p7	1:183564036	TGTTTCTGGCCTGAA[G/T]GGAAAAAGTAGGGAG	4688
rs773549355	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183580994	AAAAAAAAAAAAAAG[C/G]TGTCTACAGATTTGG	4688
rs773559932	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183573990	AGCTACTTGGGCGGC[C/T]GAGGCAGCAGAATTG	4688
rs773560368	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589789	GGTGCCTTAGAATCA[A/G]TAATCAGGTGTAAAG	4688
rs773660366	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183561483	AATTCAATGAGATGA[C/G]ATACAATAATAGTAG	4688
rs773758590	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566435	TTTGTATAGAGGTGG[C/T]ATCTCTCTATTTTGC	4688
rs773771211	snp	G/T	1.64789e-05	0.0028704	intron-variant	NCF2	GRCh38.p7	1:183560061	GTTTCTGCTAACATG[G/T]AAATTTGTTTCTATA	4688
rs773850705	in-del	-/CTT	1.64727e-05	0.00286986	cds-indel, intron-variant	NCF2	GRCh38.p7	1:183573206	CTTGCCTAGGTAATC[-/CTT]CTTGGCCAGCTGAGC	4688
rs773916860	snp	G/T	1.64735e-05	0.00286993	intron-variant	NCF2	GRCh38.p7	1:183586874	GAAATCCTCCAGTTG[G/T]TGCAACATTGAACCA	4688
rs773939641	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183569623	AGATGGAGTTTCACT[C/G]TGTCGCCCAGGCTGG	4688
rs774004164	snp	A/G	3.334e-05	0.00408276	intron-variant	NCF2	GRCh38.p7	1:183567398	TCACATGATGCCATG[A/G]CGCAAATACACTGAA	4688
rs774022827	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183556560	CCCAACCTTGACAGG[G/T]TCTCACTGTCACCCA	4688
rs774027102	snp	A/G	1.64939e-05	0.0028717	synonymous-codon	NCF2	GRCh38.p7	1:183570813	AAACCCAGAGAAACT[A/G]TCTTGATCCACCACA	4688
rs774068321	snp	C/G	1.64738e-05	0.00286995	missense	NCF2	GRCh38.p7	1:183560270	CTGGAAAGCCTTGGT[C/G]ACCCTGAAATAATAA	4688
rs774160536	snp	A/G	1.64969e-05	0.00287196	missense	NCF2	GRCh38.p7	1:183570832	TGATCCACCACAGAT[A/G]CCACGACCTAAAATC	4688
rs774230407	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183583251	TAGAGACAAGGTTTC[C/G]CCATGTTGGCCAGGC	4688
rs774251057	snp	A/G	1.65179e-05	0.00287379	intron-variant	NCF2	GRCh38.p7	1:183567171	CTGCCAGGATCCCAT[A/G]CCCATCGCACCAGCC	4688
rs774278115	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589115	CAAGCTATGTGAGAA[C/T]ATTTCAGTCACTTCT	4688
rs774302447	snp	A/G	1.64825e-05	0.00287071	intron-variant	NCF2	GRCh38.p7	1:183574656	AACATAAAACTTGAG[A/G]CTACTCCAAATCAAG	4688
rs774337221	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576036	CTATTTGGTTCTCAG[C/T]CACCTTCTCTTAAGA	4688
rs774347093	snp	C/T	1.65767e-05	0.00287891	intron-variant	NCF2	GRCh38.p7	1:183556270	GATTTCTAAAACCAC[C/T]GTAGGAAGATTACCC	4688
rs774348592	snp	C/G	3.30825e-05	0.00406696	intron-variant	NCF2	GRCh38.p7	1:183563611	AGGAAACAAAGGGAA[C/G]TCCTGAGTGTCTGAG	4688
rs774369490	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	NCF2	GRCh38.p7	1:183590255	ACTGAAGGCATCCAG[A/G]GCTCCCTTCCAGTCC	4688
rs774457345	snp	A/G	0.000131778	0.00811614	intron-variant	NCF2	GRCh38.p7	1:183569227	ACGGAAAAGGCAATG[A/G]GGGAAAGCAGGGGAG	4688
rs774513223	in-del	-/AAAG			intron-variant	NCF2	GRCh38.p7	1:183581319	AGAAAGAAAGAAAAG[-/AAAG]AAAGTCCAACAACCA	4688
rs774524948	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183577065	TGAGCAAGAGGGGAC[A/G]GATTTATGCCAAATT	4688
rs774599642	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183567348	CCCTTCCAGAGCCCT[G/T]CAGAGGATAGACACA	4688
rs774630934	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183559976	CTAGATGCTAGGAAG[A/G]GGGTTGAAAACACTG	4688
rs774648074	in-del	-/TGC			intron-variant	NCF2	GRCh38.p7	1:183560658	CCTATGAGAATCTAA[-/TGC]TGCTGCTGCTGATCT	4688
rs774655949	snp	C/G	1.73267e-05	0.0029433	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590355	AAACTAGGAGGCCAA[C/G]AGAGCTGCCAGGAGA	4688
rs774692017	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183556278	AAACCACTGTAGGAA[G/T]ATTACCCTGTCTGGC	4688
rs774701366	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584699	CGGCTGAAGGATTTG[C/T]TGTTAGGCCTCCCTG	4688
rs774719491	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183573925	CAAAACCCCGTCTCT[A/T]TTAAAAATACAAAAA	4688
rs774721138	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183560981	TCCATCCCAAAACTA[C/G]TAAATCAGAAACTCC	4688
rs774743323	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183585755	AATTATCACTTAGAA[-/T]TTTTTTCCTTTGTTA	4688
rs774842460	in-del	-/AGAT			intron-variant	NCF2	GRCh38.p7	1:183556475	TTTCAAAAAGTTACC[-/AGAT]AGATAGAGAAGAAGG	4688
rs774877800	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591788	GCCACCGTGCCCAGC[C/T]GAAATAACTTTTATG	4688
rs774918809	snp	C/G	1.6473e-05	0.00286988	missense, intron-variant	NCF2	GRCh38.p7	1:183574492	ATACGCTTACCCAGA[C/G]ACACTCCATCGCCTT	4688
rs774932046	snp	C/G	1.6477e-05	0.00287024	missense	NCF2	GRCh38.p7	1:183566934	CCTGGGGCTGCTGCT[C/G]AGGGTGGATCCGCAG	4688
rs775020616	snp	A/G	3.29473e-05	0.00405864	synonymous-codon	NCF2	GRCh38.p7	1:183577641	CCCCAGGATCTTATA[A/G]TCTATCAGCTGGTTC	4688
rs775083858	in-del	-/CC			intron-variant	NCF2	GRCh38.p7	1:183580697	AGATGTCTACAGAGG[-/CC]CGGTGCAGTGGCTCG	4688
rs775112337	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587254	ATACATATACCATCT[A/G]ATTTCTGCTTTTGTT	4688
rs775195603	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591713	ATGGTCTCGAACTCC[C/T]GACCTCAGGTGATTC	4688
rs775224104	snp	C/G	1.65154e-05	0.00287358	intron-variant	NCF2	GRCh38.p7	1:183567188	CCATCGCACCAGCCC[C/G]TGATCCTCTGCATAC	4688
rs775303126	snp	A/G	1.64817e-05	0.00287064	synonymous-codon	NCF2	GRCh38.p7	1:183563502	GACCTGGCTGTAGGG[A/G]AGCCCGGGCTGAGTC	4688
rs775374276	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183578432	GTGGGATTTCAGCTC[G/T]CTGCAAGCTCCACCT	4688
rs775489066	snp	C/T	6.5912e-05	0.00574035	missense	NCF2	GRCh38.p7	1:183566921	TGGCATCACATTACC[C/T]GGGGCTGCTGCTGAG	4688
rs775491711	snp	A/G	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183569220	AGTGAAAACGGAAAA[A/G]GCAATGAGGGAAAGC	4688
rs775538545	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568871	AGAGGGCCAATGGGA[C/T]ACCACGTAGCTGCAG	4688
rs775556290	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575327	ATACAAAAATTAGCT[A/G]GGCATGGTGGCAGGC	4688
rs775582279	in-del	-/AAC			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555826	GCACTCAGAGCAAGA[-/AAC]AACAGGATCAGTACC	4688
rs775626525	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183569572	CACATGACACTTCTG[A/C]GTATTTTTAAATTAA	4688
rs775679393	snp	C/T	1.64754e-05	0.00287009	missense	NCF2	GRCh38.p7	1:183563205	CTCACCACTGTGTTC[C/T]CACACCACAGAGTCA	4688
rs775760143	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183589011	CAGCCCCTCAGCAGG[C/T]CCCTGAGAGGAGGTG	4688
rs775786651	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584639	TATAGACTATTAGAG[A/G]TCACTAAGGAATGAC	4688
rs775879761	snp	C/T	1.64776e-05	0.00287028	intron-variant	NCF2	GRCh38.p7	1:183590122	ATAATAACAAATGCA[C/T]AGAGGAGGCCCGGAA	4688
rs775939432	in-del	-/TGAT	0.000115419	0.00759581	splice-acceptor-variant	NCF2	GRCh38.p7	1:183556231	CCATTCTTCATTCAC[-/TGAT]TGATAAAAGGAAAAG	4688
rs775961340	snp	A/C	1.64741e-05	0.00286998	intron-variant	NCF2	GRCh38.p7	1:183563326	GTGGGGATAATGAGT[A/C]AGAATCCAGTCAAAG	4688
rs776025041	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183573063	CCTATAAACAAGTCT[C/G]TCATTGCCATCCCAG	4688
rs776233541	in-del	-/TAGT			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555796	GTTTACAGTGTGAAC[-/TAGT]ACAGCTGGCTAGCTA	4688
rs776252831	snp	A/T	1.64795e-05	0.00287045	missense	NCF2	GRCh38.p7	1:183563479	AGTTTCTTAGACACC[A/T]TGTCCCGGACCTGGC	4688
rs776449371	snp	A/G	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183569101	CATCAGCTCAGGCTT[A/G]GCGCTTGGATATTCT	4688
rs776559383	snp	C/G	1.70889e-05	0.00292304	intron-variant	NCF2	GRCh38.p7	1:183567435	GCCAGGGACTTGGCT[C/G]CAGCCTGGCTCTAAC	4688
rs776600821	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183583080	TTTATTCAGACAGAA[C/T]CTTGCTCTGTTGCCC	4688
rs776639630	snp	A/G	1.64738e-05	0.00286995	intron-variant	NCF2	GRCh38.p7	1:183587000	GAGAAGGGTCCAGAC[A/G]TGGCCATGATGCAAG	4688
rs776684859	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183567369	GATAGACACAAGATC[C/G]AGCCCCCATCCCCTC	4688
rs776750922	snp	C/T	9.88419e-05	0.00702931	synonymous-codon	NCF2	GRCh38.p7	1:183565711	CCACTCACCTGGTGA[C/T]AGCTGGGGTCTTCCA	4688
rs776822572	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	NCF2	GRCh38.p7	1:183567300	CTCTTCTTTTGTCTC[A/G]GGCACAAACCCAAAT	4688
rs776843410	snp	A/G	1.6483e-05	0.00287076	intron-variant	NCF2	GRCh38.p7	1:183565786	GCTTTCCTCCTGAAG[A/G]CAACAGGGAGCGACG	4688
rs776937532	snp	A/C	0.000133477	0.00816829	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590398	AGGTTGGAGCGTCTC[A/C]CCTAGCAGGGCTGCC	4688
rs777040106	in-del	-/CTAAATCTTA			utr-variant-3-prime	NCF2	GRCh38.p7	1:183556055	TACAGCAGAAGGGTG[-/CTAAATCTTA]CTAAATCTTACAAAC	4688
rs777093765	snp	A/G	1.64749e-05	0.00287005	intron-variant	NCF2	GRCh38.p7	1:183560090	TAGTCTTGGAGTAGC[A/G]CTTACCCTTTGATAA	4688
rs777096616	in-del	-/AAAC			intron-variant	NCF2	GRCh38.p7	1:183559873	CAAAAACAAAAACAA[-/AAAC]AAAACAACTCAGCTT	4688
rs777183751	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	NCF2	GRCh38.p7	1:183560241	ATCAGCTTTTTCACT[C/T]TCCTTGGGTTCATCT	4688
rs777211162	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183585315	ACACCATGCACAGAT[C/T]ATTTTCACTGTCAGA	4688
rs777251055	snp	A/G	6.59196e-05	0.00574068	missense	NCF2	GRCh38.p7	1:183563486	TAGACACCATGTCCC[A/G]GACCTGGCTGTAGGG	4688
rs777284121	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183572192	GATTTATTATTATTA[C/T]TACTATTTTGAGATG	4688
rs777308655	snp	A/G	3.29468e-05	0.00405861	intron-variant	NCF2	GRCh38.p7	1:183586983	TGGTAAAGGCCTGAG[A/G]AGAGAAGGGTCCAGA	4688
rs777388957	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580126	TCACCATTAGGGTTG[A/G]GGTAAGTCACACATG	4688
rs777409864	snp	G/T	1.64727e-05	0.00286986	intron-variant	NCF2	GRCh38.p7	1:183569189	AGGCTCAGCTGCCTA[G/T]TGAACATTCAGGAGA	4688
rs777472215	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183584490	AATTGAATCCTGGGT[A/C]TTACTTTTAGAAGTT	4688
rs777507234	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573269	GCCCACAGGGATCAC[C/T]ACTGGCTCATATAGC	4688
rs777562994	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183588704	ATGAATAAGAATGCA[C/T]ATAAATGCTAGTAGG	4688
rs777594849	snp	A/C	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183574465	GACATCCTCTCAACA[A/C]CTGCATCACCAATAC	4688
rs777609586	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560764	GGTTGGGGACCCCTG[A/G]GATAAATGAAACCAA	4688
rs777621636	in-del	-/G	1.64773e-05	0.00287026	frameshift-variant	NCF2	GRCh38.p7	1:183566940	GCTGCTGCTGAGGGT[-/G]GATCCGCAGCTCAAC	4688
rs777651231	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578686	ATAGTTTTTCTAATG[C/T]TGCTCCCACTGCCTT	4688
rs777651789	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183562045	GGCATGAGCCACTGC[G/T]CCTGGTTTTCTTTCT	4688
rs777826252	in-del	-/G	1.65218e-05	0.00287413	intron-variant	NCF2	GRCh38.p7	1:183563592	CTTCACTTCCTGAGT[-/G]GGGAGGAAACAAAGG	4688
rs777845732	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183565353	TTGAAAACAGCCACT[C/G]CATGCCCCTCAGAGA	4688
rs777856745	snp	A/G			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555871	GTGCCCTTTCCAGAC[A/G]CTTCCATCCACTTTT	4688
rs777953876	snp	C/G	1.65677e-05	0.00287812	intron-variant	NCF2	GRCh38.p7	1:183567375	CACAAGATCCAGCCC[C/G]CATCCCCTCACATGA	4688
rs778031407	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568550	AAGAAAGCTGTAGGT[C/T]ATGTCACCCTTTGTT	4688
rs778038706	snp	A/G	3.29853e-05	0.00406098	intron-variant	NCF2	GRCh38.p7	1:183563151	AATTGTTGAGGAAGT[A/G]GCTCAGTGGAAATGT	4688
rs778131800	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591374	CTTTTTTGTAATCCC[A/G]TAGGCTGTATTAATA	4688
rs778259155	snp	C/G	1.64738e-05	0.00286995	synonymous-codon	NCF2	GRCh38.p7	1:183577623	AAACAGCTTGAACTG[C/G]AGCCCCAGGATCTTA	4688
rs778421718	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183580360	TACGCCAGAAATCAG[G/T]TTCCGCTTTCTAAGC	4688
rs778424859	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183583336	TGGGATTACAGGTGT[G/T]AGCCACTGTGCCCAG	4688
rs778431195	snp	A/G	3.2981e-05	0.00406071	synonymous-codon	NCF2	GRCh38.p7	1:183567264	CAAGACAAAGACAAT[A/G]TTCCCTGGCATGACC	4688
rs778511922	snp	C/G	1.64811e-05	0.00287059	intron-variant	NCF2	GRCh38.p7	1:183560315	TTCCCAATTTCCTGC[C/G]AAGTGAACACTGAAC	4688
rs778521448	snp	C/T	6.58957e-05	0.00573964	missense	NCF2	GRCh38.p7	1:183565758	GAGGAGCTGGGATGT[C/T]GGACTGCGGAGAGCT	4688
rs778540553	snp	A/G	1.72812e-05	0.00293944	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590452	TTTCTGGGCCAGATG[A/G]GTAGAATGGGGCCCA	4688
rs778546412	snp	C/T	3.29451e-05	0.00405851	missense	NCF2	GRCh38.p7	1:183586958	AAGTGCTTGTCTCGG[C/T]TAATGCTTCTGGTAA	4688
rs778645987	in-del	-/ACAA			utr-variant-3-prime	NCF2	GRCh38.p7	1:183556064	AGGGTGCTAAATCTT[-/ACAA]ACAAACAAGTAATAG	4688
rs778751639	in-del	-/CTT	3.29995e-05	0.00406185			GRCh38.p7	1:183567243	CCAGTTATCATTGCC[-/CTT]CTTCAAGACAAAGAC	4688
rs778760117	snp	C/T					GRCh38.p7	1:183573605	TAGAGGGCACCACCA[C/T]GACAAGGCTGGCCCG	4688
rs778842195	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183559404	GTTTTTAAGGCAAAA[G/T]TTACCTACTTTTCTC	4688
rs778858758	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560659	CCTATGAGAATCTAA[C/T]GCTGCTGCTGATCTG	4688
rs778911214	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573248	CTCATTTGGTCGAAA[C/T]AGCTTGCCCACAGGG	4688
rs778995405	snp	A/C	1.64754e-05	0.00287009	intron-variant	NCF2	GRCh38.p7	1:183564058	AGTAGGGAGTAAAAC[A/C]AAAGAAGATGGTGAA	4688
rs779084727	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568347	AATTTTTTCATGTTT[A/G]GTAGACATGGGGTTT	4688
rs779087160	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574562	GGCCAATGCTAACTG[C/T]TCTTCAGCTTTTTTC	4688
rs779088549	snp	A/G	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183586901	ACCACTTACTTCTCT[A/G]TCTGGTAGTAGAGCA	4688
rs779146059	snp	A/G			downstream-variant-500B	NCF2	GRCh38.p7	1:183555551	GGTTCTGTTTAAGCA[A/G]CAAGACATAATGAAA	4688
rs779164147	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591935	CTGCACTGATGACTA[A/G]TGGATTTACTAGTCT	4688
rs779174856	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183574900	AAGAATTATTGTATA[C/G]AGTGTGTTCAAACCA	4688
rs779188117	snp	G/T	1.64732e-05	0.0028699	missense	NCF2	GRCh38.p7	1:183560198	GGCTGCCTTTCTTAA[G/T]CTGAGGTTCTGTTGT	4688
rs779290545	snp	A/G	6.64132e-05	0.00576213	intron-variant	NCF2	GRCh38.p7	1:183570760	ACCTAGGTCCATGGA[A/G]AAGGTCAGGACTGCC	4688
rs779303160	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183557330	TTTAATGTGTGGTGT[C/G]ACTGGGCAGCAGTTT	4688
rs779365986	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587864	AATAAAAAATACATA[C/T]CTATATTTAAAATAT	4688
rs779385352	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183557630	CAATATGGGTATTTC[C/G]TCAACTTAGACTTGT	4688
rs779573048	snp	A/C	1.64741e-05	0.00286998	missense, intron-variant	NCF2	GRCh38.p7	1:183574598	CTCCTTCTTGGCATA[A/C]ATGAAAGCAATGTTA	4688
rs779658024	in-del	-/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555783	ACAGCTTGATGAATG[-/T]TTACAGTGTGAACAC	4688
rs779867537	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	NCF2	GRCh38.p7	1:183560163	TTGGGTAGCCTCATA[A/G]CTGAAGAGTGCCTCC	4688
rs779927196	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570613	ATTTCCTCACCAGCC[A/G]TGGAAACCAGGACTG	4688
rs779931479	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557585	CTGTCCTACCCTGAC[C/T]GCTAAATTCTGTTTT	4688
rs780050246	snp	C/G	4.3321e-05	0.00465388	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590428	CTTAGTGGCCCCCAA[C/G]GTGTTCACTTTCTGG	4688
rs780053247	snp	A/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183590995	TTGAATGTTGCCTTT[A/T]CCAGTACTACCTATG	4688
rs780058052	snp	C/G	1.65899e-05	0.00288005	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590335	CCAGGGACATGATTA[C/G]GTAGAAACTAGGAGG	4688
rs780154260	snp	C/T	1.64933e-05	0.00287165	synonymous-codon	NCF2	GRCh38.p7	1:183570816	CCCAGAGAAACTGTC[C/T]TGATCCACCACAGAT	4688
rs780190814	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183559303	TAGTGGCTAGGATTA[C/T]AGGCATGCTGTTTCA	4688
rs780235098	snp	A/T	1.64732e-05	0.0028699	missense, intron-variant	NCF2	GRCh38.p7	1:183574571	TAACTGTTCTTCAGC[A/T]TTTTTCCATTCCTCC	4688
rs780269537	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183568262	CCACCTCCTGAGTGC[A/G]AGTGAGCCTCCTGCC	4688
rs780274152	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183583904	TTTTACAAGATCACT[A/C]TGGAATATGAATGGA	4688
rs780275172	in-del	-/TTTTTTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561780	ACCATACCAGGCCTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4688
rs780354190	snp	A/G	2.69997e-05	0.00367411	intron-variant	NCF2	GRCh38.p7	1:183567512	CTCCCAAGAGGTCTC[A/G]GCAAGAAACTGGTGT	4688
rs780392681	in-del	-/TTTTTTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561781	CCATACCAGGCCTCT[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4688
rs780442146	snp	A/G	3.29451e-05	0.00405851	missense	NCF2	GRCh38.p7	1:183569173	TTTTCGGTCTGGGTG[A/G]AGGCTCAGCTGCCTA	4688
rs780651962	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566696	ACAGAGGTGGGTGGG[C/T]CCAATGGGACCTACA	4688
rs780693222	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560877	TATTTCTTTACAGAT[A/G]GGGACAGAGCCCTAA	4688
rs780702980	snp	A/G	1.65004e-05	0.00287227	missense	NCF2	GRCh38.p7	1:183563561	CCTTGAGTGTGTAGG[A/G]CATGGGAACACTGAG	4688
rs780711902	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183563165	TGGCTCAGTGGAAAT[A/G]TAACTTTAGATGCCC	4688
rs780715462	snp	A/G	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183569212	TCAGGAGAAGTGAAA[A/G]CGGAAAAGGCAATGA	4688
rs780810631	snp	G/T	1.65479e-05	0.0028764	missense	NCF2	GRCh38.p7	1:183590329	CCTCCACCAGGGACA[G/T]GATTAGGTAGAAACT	4688
rs780880666	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183582699	GTTTCCAAGTCAGCA[A/G]GAAGAAGGCTTTGCT	4688
rs780881727	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183573763	CAAATATGCTTGAAC[A/G]ATAAATAGTTTTTAT	4688
rs780898644	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561921	TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA	4688
rs780899104	snp	C/T	1.67024e-05	0.0028898	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556088	GTAATAGGGCTTCAT[C/T]TTCTTCAGCTTTGTA	4688
rs780956846	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183586663	GGTGGTTACCTAGGC[C/T]CATTGTGCCTATGAC	4688
rs781012673	snp	A/T	1.65589e-05	0.00287736	intron-variant	NCF2	GRCh38.p7	1:183567030	AAGGAAAAAATAAAG[A/T]TGTGCTCATCAGTAC	4688
rs781157423	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183563882	CATGGACTCTGTAAG[A/G]TAGCAACTGGTTCGA	4688
rs781265077	in-del	-/A			downstream-variant-500B	NCF2	GRCh38.p7	1:183555125	ACACTGATGATACTT[-/A]ACTTACCATTGTGGT	4688
rs781271218	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557687	CTGGCTTCTCTCCAT[A/G]TCTACCCAAAAGGTT	4688
rs781319150	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183570446	GGCTTTGTTAATAAG[C/T]CTTCCATAGCTTGTG	4688
rs781431052	snp	A/G	1.6492e-05	0.00287154	synonymous-codon	NCF2	GRCh38.p7	1:183556121	TTGTGAAACATCCTA[A/G]ACTTCTCTCCGAGTG	4688
rs781553916	snp	A/G	6.49063e-05	0.0056964	intron-variant	NCF2	GRCh38.p7	1:183567490	GATGACACTGAGCCT[A/G]CCTGGGCTCCCAAGA	4688
rs781704576	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589675	TTATAATTGATCAGA[A/G]TTGTCACTTGGGATA	4688
rs781712989	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183566561	ATTTTCTTTCTAATG[A/G]CATTGTACCAGCCAA	4688
rs781757344	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575822	AAACTCAGACAGGTG[A/G]AAGGATTGATGTTTC	4688
rs781765998	snp	A/T	1.64779e-05	0.00287031	intron-variant	NCF2	GRCh38.p7	1:183563189	GATGCCCCTCATTGC[A/T]CTCACCACTGTGTTC	4688
rs781779880	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576551	ACAACCCCTCTCTCG[C/T]CTCTGCTACAATACA	4688
rs796065030	in-del	-/GA			frameshift-variant, intron-variant	NCF2	GRCh38.p7	1:183574587	TCATGTATGCCAAGA[-/GA]AGGAGGAATGGAAAA	4688
rs796065031	in-del	-/AAGCT			frameshift-variant	NCF2	GRCh38.p7	1:183563437	CGGCTGGAACACACT[-/AAGCT]GAGGTGAGCTCCATG	4688
rs796065032	snp	A/G			splice-donor-variant	NCF2	GRCh38.p7	1:183577598	CTGTTTGCCTGTGAG[A/G]TAAGGAGAACAGGGC	4688
rs796065033	in-del	-/AAGAAGGAC			cds-indel	NCF2	GRCh38.p7	1:183590267	GTGCTGGCAGCGGAC[-/AAGAAGGAC]TGGAAGGGAGCCCTG	4688
rs796137314	multinucleotide-polymorphism	AG/GA			intron-variant	NCF2	GRCh38.p7	1:183581314	AAGAAAGAAAGAAAG[AG/GA]AAGAAAGTCCAACAA	4688
rs796331762	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183558966	GGTAGTGCACAGACT[C/T]AGCGTATGAGCAGGG	4688
rs796341683	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183578567	GACCAGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	4688
rs796380647	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183556426	ATCTGTCTTAAACAT[A/G]ATAATGAGCAAAATG	4688
rs796416120	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183582026	CTTCCCAGCCCCCTC[A/G]TTCCCTGCTGCAGGC	4688
rs796710510	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183557881	TTACTACTACTCATA[-/T]TTTTTTTTTTTGAGA	4688
rs796718600	multinucleotide-polymorphism	GCC/TCT			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592387	ATCTAGCCCTGAACT[GCC/TCT]GGTAGTAGGAGAATT	4688
rs796794395	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183567721	GGTCAGGGGAACAGC[A/T]CAAAGCAGAAGTCAG	4688
rs796907871	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561476	CTAGAAGAATTCAAT[A/G]AGATGACATACAATA	4688

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