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

NCF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs800977	snp	C/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74781492	ataataataataata[C/T]ctaacattaatggag	653361
rs800978	snp	A/G	0.23031	0.249223	intron-variant	NCF1	GRCh38.p7	7:74781743	tcactacattgccca[A/G]gctggtcttaaactc	653361
rs800979	snp	A/G	0.466412	0.125164	intron-variant	NCF1	GRCh38.p7	7:74781755	ccaagctggtcttaa[A/G]ctcttggcctcaagc	653361
rs800980	snp	C/T	0.161267	0.233723	intron-variant	NCF1	GRCh38.p7	7:74781899	ctgacctcattttaa[C/T]ttaattacctcttga	653361
rs800981	snp	C/T	0.214239	0.247429	intron-variant	NCF1	GRCh38.p7	7:74782019	gatgtcagccaataC[C/T]Aaacagcatcagcac	653361
rs997440	snp	A/G	0.5	0	intron-variant	NCF1	GRCh38.p7	7:74786460	ttgctctgactccca[A/G]gctggagcacaatca	653361
rs1637415	snp	C/T	0.0654984	0.168698	intron-variant	NCF1	GRCh38.p7	7:74775890	aggtgcgcgccacca[C/T]gcccagctcgcattt	653361
rs2465932	snp	G/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74785746	acatgagccgggtgt[G/T]gtggtgggagcctgt	653361
rs2472047	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74785652	ctttgggagcccagg[A/G]caggacgatcacgtg	653361
rs2472048	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74785664	agggcaggacgatca[C/T]gtgaggtcaggagtt	653361
rs2523327	snp	C/T	0.142012	0.225474	intron-variant	NCF1	GRCh38.p7	7:74781945	acctttctcttaata[C/T]acccacactgtaagg	653361
rs2523332	snp	A/T	0.276443	0.248598	intron-variant	NCF1	GRCh38.p7	7:74783255	TGTGGGCATCTGTGC[A/T]TGGCAGGCCGGGGCG	653361
rs2523333	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74784449	tgagacaaagtctgg[C/T]tctgtcacccaggct	653361
rs2523335	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74787450	tgtctTGGGGTTGGG[C/T]GGGGGAAAAGCATTT	653361
rs2528941	snp	A/G	0.435837	0.167226	intron-variant	NCF1	GRCh38.p7	7:74783387	GTGACCTCATTGTCC[A/G]GTGTGGTGAAGGTGA	653361
rs2529296	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74777234	GCCTCTTTGGAGGCT[A/G]AATGGGGTCCCCCGA	653361
rs2529297	snp	A/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74782015	ggcggatgtcagccA[A/T]TACTAaacagcatca	653361
rs2539044	snp	C/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74788173	TGAGAGCCCCCGCCC[C/T]GGCACTGCCAAGCTA	653361
rs2718280	snp	C/T	0.395087	0.203592	downstream-variant-500B	NCF1	GRCh38.p7	7:74789738	GAGGATCCGTTGAGC[C/T]CAGGAGTTCGAGACC	653361
rs2737400	snp	A/C			intron-variant	NCF1	GRCh38.p7	7:74782581	agaccttgtctttac[A/C]agaaattagccgggt	653361
rs2737401	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74782583	accttgtctttacca[A/G]aaattagccgggtgt	653361
rs2906281	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74776039	GCATCCTCCGCCTCC[C/T]AGGTTCAAGCAATTC	653361
rs2953669	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74775973	tttttatgagatgga[G/T]tcttactctgtcacc	653361
rs2953670	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74775998	gtcacccaggctgga[G/T]tgcaatggcacaatc	653361
rs17356100	snp	A/G	0.00137622	0.0261957	synonymous-codon	NCF1	GRCh38.p7	7:74779372	CACCTTGAAGAAGTC[A/G]AGGAGGTGGGGACAG	653361
rs28668454	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74782204	AGCACTTTGGGAGGC[C/T]GAGGCGGTTGAATCA	653361
rs35067650	snp	C/T	0.1638	0.234669	intron-variant	NCF1	GRCh38.p7	7:74785057	GAAGAGGGGGAACTG[C/T]GGGCCCTGGGTGGGT	653361
rs60312903	in-del	-/A			intron-variant	NCF1	GRCh38.p7	7:74786255	AAAAAAAAAAAAAAA[-/A]GCTTCCATTGCAATT	653361
rs62475422	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74778615	TGCTGGTGACTTGCA[C/T]ATGGGAGGGAGAGAG	653361
rs62475427	snp	C/G			utr-variant-3-prime	NCF1	GRCh38.p7	7:74789202	TCTCGGCCCTTGCCG[C/G]CCCGTGCCTGTACAT	653361
rs75207809	snp	A/T	0	0	intron-variant	NCF1	GRCh38.p7	7:74775961	AGTCTTTTTTTTTTT[A/T]TATGAGATGGAGTCT	653361
rs77875067	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	NCF1	GRCh38.p7	7:74789533	AGAAACCACCTGCTT[A/G]GACTCTGGCGGAAGA	653361
rs78031146	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74779032	GTGATTTTCCAAGTG[C/T]TGTAAACTACAAATA	653361
rs111979289	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772242	CAGGAGATCAGGTCC[A/G]GACCATGAGCTGACC	653361
rs112000369	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74783077	GTCAGACCTCCCACC[C/T]TACGGGGCTCCTTCC	653361
rs112894340	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74777495	TTTATTTATATAAAT[G/T]TTTGTGACAGGGTCT	653361
rs113297930	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74775965	TTTTTTTTTTTTTAT[A/G]AGATGGAGTCTTACT	653361
rs113623758	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74787032	AGATGGATTTCCATA[C/T]TGGAAAAAAAAAAAA	653361
rs119103270	snp	A/G			missense	NCF1	GRCh38.p7	7:74777319	AGAAGGTGGTCTACC[A/G]GCGCTTCACCGAGAT	653361
rs119103271	snp	C/T			stop-gained	NCF1	GRCh38.p7	7:74779298	GCCGCCGAGAACCGC[C/T]AGGGCACACTTACCG	653361
rs119103272	snp	A/T	3.56831e-05	0.00422377	NCF1	7	allele_origin=T(germline)/A(germline)	7:74779360	CAAGATCTCCCGCTG[A/T]CCCCACCTCCTCGAC	653361
rs119103273	snp	A/G	6.84521e-05	0.0058499	NCF1	7	allele_origin=G(germline)/A(germline)	7:74783061	GAGAAGAGCGAGAGC[A/G]GTCAGACCTCCCACC	653361
rs138054188	snp	C/T	0.0532157	0.154195	intron-variant	NCF1	GRCh38.p7	7:74775882	GGGAATACAGGTGCG[C/T]GCCACCATGCCCAGC	653361
rs138406096	snp	A/G	0.0185938	0.0946107	intron-variant	NCF1	GRCh38.p7	7:74785612	TCCTAGCTAGGCGCA[A/G]TGGCTCAGGCCTGTA	653361
rs139225348	snp	A/G	0.0179533	0.0930287	missense	NCF1	GRCh38.p7	7:74779274	CCCAAGTGGTTTGAC[A/G]GGCAGCGGGCCGCCG	653361
rs140034807	snp	A/G	0.0379877	0.132479	intron-variant	NCF1	GRCh38.p7	7:74775881	TGGGAATACAGGTGC[A/G]CGCCACCATGCCCAG	653361
rs140463577	snp	C/T	0.000408956	0.0142937	synonymous-codon	NCF1	GRCh38.p7	7:74783060	AGAGAAGAGCGAGAG[C/T]GGTCAGACCTCCCAC	653361
rs140969778	snp	A/G	0.00358779	0.0422022	intron-variant	NCF1	GRCh38.p7	7:74781714	ATTTTTAATTTTCTG[A/G]TAGAGATGGGGTCTC	653361
rs141286916	snp	A/C			intron-variant	NCF1	GRCh38.p7	7:74787053	AAAAAAAAAAAAGAG[A/C]AAAAAACAAACCTAG	653361
rs141305543	snp	A/G			upstream-variant-2KB	NCF1	GRCh38.p7	7:74773052	AAAAAAAAAAAATTA[A/G]CCAGGTGTGGTGGCA	653361
rs142050799	snp	C/T	0.00398564	0.0444627	intron-variant	NCF1	GRCh38.p7	7:74777567	AGGCATGAGCCCCCA[C/T]GCTCGGCCTTTTAGG	653361
rs142480486	snp	A/G	0.000340248	0.0130387	missense	NCF1	GRCh38.p7	7:74782989	GCCATTGCCAACTAC[A/G]AGAAGACCTCGGGCT	653361
rs144018361	snp	G/T	0.00145853	0.0269655	missense	NCF1	GRCh38.p7	7:74779319	ACACTTACCGAGTAC[G/T]GCGGCACGCTCATGA	653361
rs144372615	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74775883	GGAATACAGGTGCGC[A/G]CCACCATGCCCAGCT	653361
rs145360423	snp	A/G	0.00129198	0.0253835	stop-gained	NCF1	GRCh38.p7	7:74783529	CTCTGGCACAGGTTG[A/G]TGGTTCTGTCAGATG	653361
rs146125534	snp	C/T	0.00887071	0.0660051	missense	NCF1	GRCh38.p7	7:74779326	CCGAGTACTGCGGCA[C/T]GCTCATGAGCCTGCC	653361
rs146173318	snp	A/G	0.000524761	0.0161897	synonymous-codon	NCF1	GRCh38.p7	7:74777302	ATGGCAGGACCTGTC[A/G]GAGAAGGTGGTCTAC	653361
rs147659773	snp	C/T	8.5139e-05	0.00652397	missense	NCF1	GRCh38.p7	7:74783606	ACAGTCCTGACGAGA[C/T]GGAAGACCCTGAGCC	653361
rs148767467	snp	C/T	9.10258e-05	0.00674571	missense	NCF1	GRCh38.p7	7:74779355	CCCACCAAGATCTCC[C/T]GCTGTCCCCACCTCC	653361
rs149204001	snp	A/G			missense	NCF1	GRCh38.p7	7:74783602	CTGGACAGTCCTGAC[A/G]AGACGGAAGACCCTG	653361
rs151319713	snp	A/G	6.69299e-05	0.0057845	synonymous-codon	NCF1	GRCh38.p7	7:74783051	GGAGGTCGTAGAGAA[A/G]AGCGAGAGCGGTCAG	653361
rs181692881	snp	A/G	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74782011	AGAAGGCGGATGTCA[A/G]CCAATACCAAACAGC	653361
rs181788842	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74781963	CCACACTGTAAGGTA[C/T]TGGGTGGTTAGGACT	653361
rs182413790	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785865	TCCAGCCTGGGCAAC[A/G]AGAGCGAAACTCCGT	653361
rs183580334	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74777569	GCATGAGCCCCCACG[C/G]TCGGCCTTTTAGGTG	653361
rs185170050	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787238	ATGTCAGGAGTTTGA[A/G]ACCAGCCATGACCAA	653361
rs185872833	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74782002	TGAATTTTGAGAAGG[C/T]GGATGTCAGCCAATA	653361
rs190079672	snp	A/G	0.00279162	0.0372561	intron-variant	NCF1	GRCh38.p7	7:74782003	GAATTTTGAGAAGGC[A/G]GATGTCAGCCAATAC	653361
rs199789198	snp	A/C	0.0154538	0.0865337	intron-variant	NCF1	GRCh38.p7	7:74781840	GCCCGGCTTTTTCTT[A/C]TTCTTATAAGGACAC	653361
rs199886863	snp	G/T	0.00106549	0.0230566	intron-variant	NCF1	GRCh38.p7	7:74777359	CCATGTGAGTGTGGG[G/T]ACGGAGGAGGGACAG	653361
rs199908473	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74784586	CACGCCAGGCTAATT[G/T]TTTGTATTTTTAGTA	653361
rs199938434	snp	C/T	6.90286e-05	0.00587448	synonymous-codon	NCF1	GRCh38.p7	7:74779285	TGACGGGCAGCGGGC[C/T]GCCGAGAACCGCCAG	653361
rs200050981	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74778391	CCTCCCAAATTGCTA[C/G]GATTACAGGTTTGAG	653361
rs200205449	snp	A/G	0.499977	0.00339449	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773424	TGATCCCACCACTGC[A/G]CTTAAGCCTGGATAA	653361
rs200459715	snp	G/T	0.00123077	0.0247764	intron-variant	NCF1	GRCh38.p7	7:74782896	CTGGAGGCCCAGATG[G/T]GCCCTGCAATGCCCA	653361
rs200623471	snp	A/G	0.22263	0.248497	intron-variant	NCF1	GRCh38.p7	7:74778736	atggagtgcagtggc[A/G]ccatctcggctcact	653361
rs200655630	in-del	-/A	0.49263	0.0602539	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773035	ACCCAGTCTCTAATT[-/A]AAAAAAAAAAAAATT	653361
rs200663210	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777247	CTGAATGGGGTCCCC[C/T]GACTCTGGCTTTCCC	653361
rs201522178	snp	A/G	0.000497934	0.0157708	missense	NCF1	GRCh38.p7	7:74782972	TCCTGCAGACGTACC[A/G]CGCCATTGCCAACTA	653361
rs201586849	snp	A/T			intron-variant	NCF1	GRCh38.p7	7:74775963	TCTTTTTTTTTTTTT[A/T]TGAGATGGAGTCTTA	653361
rs201802880	snp	A/G	0.00208105	0.03219	missense	NCF1	GRCh38.p7	7:74779296	GGGCCGCCGAGAACC[A/G]CCAGGGCACACTTAC	653361
rs201978343	snp	C/T			downstream-variant-500B	NCF1	GRCh38.p7	7:74789697	GGCTCACGCCTGTAA[C/T]CCAGCACTTTGGGAG	653361
rs202195500	snp	C/T	0.000187606	0.00968337	missense	NCF1	GRCh38.p7	7:74782981	CGTACCGCGCCATTG[C/T]CAACTACGAGAAGAC	653361
rs273585651	in-del	-/GT			frameshift-variant	NCF1	GRCh38.p7	7:74777269	GGCTTTCCCCCAGGT[-/GT]ACATGTTCCTGGTGA	653361
rs367985113	snp	A/G	0.000627254	0.0176984	missense	NCF1	GRCh38.p7	7:74782974	CTGCAGACGTACCGC[A/G]CCATTGCCAACTACG	653361
rs368254704	snp	A/G	0.000137872	0.00830161	intron-variant	NCF1	GRCh38.p7	7:74777248	TGAATGGGGTCCCCC[A/G]ACTCTGGCTTTCCCC	653361
rs368358726	snp	C/T			upstream-variant-2KB	NCF1	GRCh38.p7	7:74772150	CTTGGGCAACAAGAG[C/T]GAAACTTCGCTTCAA	653361
rs368662637	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74781827	CATGAGCCACTGTGC[C/T]CGGCTTTTTCTTCTT	653361
rs368945669	snp	C/G	3.35272e-05	0.0040942	synonymous-codon	NCF1	GRCh38.p7	7:74783018	CTCCGAGATGGCTCT[C/G]TCCACGGGGGACGTG	653361
rs368948045	snp	A/T	0.000153988	0.00877328	missense	NCF1	GRCh38.p7	7:74777337	GCTTCACCGAGATCT[A/T]CGAGTTCCATGTGAG	653361
rs369249526	snp	C/T	0.000153988	0.00877328	synonymous-codon	NCF1	GRCh38.p7	7:74783042	GGACGTGGTGGAGGT[C/T]GTAGAGAAGAGCGAG	653361
rs369461764	snp	A/G	0.00660348	0.0570801	intron-variant	NCF1	GRCh38.p7	7:74779228	CTCCCAGCCCCTCTC[A/G]GGCTTGACCTCATGT	653361
rs369485834	snp	A/G	0.208474	0.246527	intron-variant	NCF1	GRCh38.p7	7:74784878	ACCTTCATCGTTATG[A/G]GATCTCTGGTCCCCA	653361
rs370513174	snp	A/C/T	0.000397452	0.0140914	intron-variant	NCF1	GRCh38.p7	7:74779428	CGGACAACCAGTGAG[A/C/T]GAACTTTTCACCCTG	653361
rs371061025	snp	C/G			intron-variant	NCF1	GRCh38.p7	7:74781786	AACCCTCCTGCCTCA[C/G]CCTCCCAAAGTGCTG	653361
rs371075194	snp	A/G	6.55645e-05	0.0057252	synonymous-codon	NCF1	GRCh38.p7	7:74779327	CGAGTACTGCGGCAC[A/G]CTCATGAGCCTGCCC	653361
rs371241620	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74785449	TCAGTAGCAGGGAGG[A/G]ATGAGCCCACCCTTG	653361
rs372176579	snp	A/G	1.6588e-05	0.00287988	missense	NCF1	GRCh38.p7	7:74783037	ACGGGGGACGTGGTG[A/G]AGGTCGTAGAGAAGA	653361
rs372181124	snp	C/T	0.00358779	0.0422022	intron-variant	NCF1	GRCh38.p7	7:74784210	CTGGGATTACAAGCA[C/T]GCACCACCATGCCTG	653361
rs372741570	snp	A/G	0.000153988	0.00877328	missense	NCF1	GRCh38.p7	7:74783569	CGAGGCTGGATCCCA[A/G]CGTCCTTCCTCGAGC	653361
rs373093123	snp	A/G	3.44317e-05	0.00414906	missense	NCF1	GRCh38.p7	7:74779281	GGTTTGACGGGCAGC[A/G]GGCCGCCGAGAACCG	653361
rs373132324	snp	A/G	0.000216939	0.0104126	missense	NCF1	GRCh38.p7	7:74779356	CCACCAAGATCTCCC[A/G]CTGTCCCCACCTCCT	653361
rs373480987	snp	A/C/G	8.27581e-05	0.0064322	intron-variant	NCF1	GRCh38.p7	7:74777363	GTGAGTGTGGGGACG[A/C/G]AGGAGGGACAGGGAC	653361
rs373919021	snp	C/G/T	0.0833678	0.18641	intron-variant	NCF1	GRCh38.p7	7:74780862	GGGGCAGCCGGCGGG[C/G/T]GGGGGACACCCTGAG	653361
rs374263357	snp	C/T	6.87829e-05	0.00586402	synonymous-codon	NCF1	GRCh38.p7	7:74783006	GAAGACCTCGGGCTC[C/T]GAGATGGCTCTGTCC	653361
rs374384176	snp	G/T	2.12583e-05	0.00326017	missense	NCF1	GRCh38.p7	7:74779333	CTGCGGCACGCTCAT[G/T]AGCCTGCCCACCAAG	653361
rs374969926	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74777616	AGGTTTGCAGTGCAG[A/G]GGCGCAATCATAGCT	653361
rs375011835	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784638	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	653361
rs375851395	snp	C/T	0.000117908	0.00767723	synonymous-codon	NCF1	GRCh38.p7	7:74777297	GTGAAATGGCAGGAC[C/T]TGTCGGAGAAGGTGG	653361
rs376071195	snp	G/T			intron-variant	NCF1	GRCh38.p7	7:74781789	CCTCCTGCCTCAGCC[G/T]CCCAAAGTGCTGAGA	653361
rs376454321	snp	A/G	0.000104082	0.00721319	missense	NCF1	GRCh38.p7	7:74779374	GTCCCCACCTCCTCG[A/G]CTTCTTCAAGGTGCG	653361
rs376919169	snp	C/G/T	6.73246e-05	0.00580159	missense, synonymous-codon	NCF1	GRCh38.p7	7:74783601	CCTGGACAGTCCTGA[C/G/T]GAGACGGAAGACCCT	653361
rs377305075	snp	A/C	0.00075293	0.0193881	intron-variant	NCF1	GRCh38.p7	7:74777264	ACTCTGGCTTTCCCC[A/C]AGGTGTACATGTTCC	653361
rs377576524	snp	C/T	7.8883e-05	0.00627975	synonymous-codon	NCF1	GRCh38.p7	7:74779309	CCGCCAGGGCACACT[C/T]ACCGAGTACTGCGGC	653361
rs377662255	snp	C/T	0.0301723	0.119062	intron-variant	NCF1	GRCh38.p7	7:74777383	GGGACAGGGACCCAC[C/T]GTTCCAGCTCCACCC	653361
rs587594457	snp	C/T	0.0020364	0.0318442	synonymous-codon	NCF1	GRCh38.p7	7:74788589	CGCGCACAGCATCCA[C/T]CAGCGGTCGCGGAAG	653361
rs587595128	snp	C/T	3.4424e-05	0.00414859	intron-variant	NCF1	GRCh38.p7	7:74779253	TCATGTTCTCTGGTG[C/T]CAGCTCCCAAGTGGT	653361
rs587596880	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772241	CCAGGAGATCAGGTC[C/T]GGACCATGAGCTGAC	653361
rs587597258	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74781918	ATTACCTCTTGAAAC[A/G]TACTTAAGAGTACCT	653361
rs587598319	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772353	CCCGCCACTCATGAA[C/T]TCATGACCTTGAATG	653361
rs587598401	snp	C/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74778375	GATCCTCCCGCCTCA[C/G]CCTCCCAAATTGCTA	653361
rs587599110	snp	A/C	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74776871	GTGCGGCACCACACC[A/C]GGACAATTTTTGTGT	653361
rs587599132	snp	C/T	0.00438332	0.0466095	intron-variant	NCF1	GRCh38.p7	7:74786588	AGGGATGGGGTCTCA[C/T]TATGGTGCCAAGACT	653361
rs587599860	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74784876	AGACCTTCATCGTTA[C/T]GGGATCTCTGGTCCC	653361
rs587600267	snp	A/G	0.00318978	0.0398085	intron-variant	NCF1	GRCh38.p7	7:74783764	GGCTAAGATCTCATC[A/G]ACTCTGGCTTGGGGG	653361
rs587602527	snp	A/G	4.29037e-05	0.00463142	intron-variant	NCF1	GRCh38.p7	7:74783081	GACCTCCCACCTTAC[A/G]GGGCTCCTTCCCCTG	653361
rs587602716	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784725	GCCCAGCCTGTGGCT[A/G]TCGTTTAAACACTGG	653361
rs587603740	snp	C/T	0.00294069	0.0382321	synonymous-codon	NCF1	GRCh38.p7	7:74782946	TGCCCCAGACATCAC[C/T]GGCCCCATCATCCTG	653361
rs587605880	snp	A/C	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74783831	AACCAGGAGGAGGAG[A/C]AGACGACTGGGGAGA	653361
rs587606175	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772146	CCAGCTTGGGCAACA[A/G]GAGCGAAACTTCGCT	653361
rs587609606	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74786477	CTGGAGCACAATCAT[C/T]GCTCACTCAAGCGAT	653361
rs587612525	snp	A/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777042	TCTCCAATTTACAGA[A/T]GAGTCCATTTGAGAG	653361
rs587612790	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74778743	GCAGTGGCGCCATCT[C/T]GGCTCACTGTAACCT	653361
rs587614686	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782542	TGAGCCCAGGAGTTC[A/G]AGACCAGCCTGGGCA	653361
rs587615323	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74775940	TGCCATATTGATTCT[A/G]GATCAGTCTTTTTTT	653361
rs587616286	snp	C/G	0.0551013	0.156571	intron-variant	NCF1	GRCh38.p7	7:74783439	GACATCAGTGTGTCT[C/G]TGTCCCTGTGTCCTC	653361
rs587616925	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74783270	TTGGCAGGCCGGGGC[A/G]GGGCATGTCTGCGTG	653361
rs587618080	snp	A/G	0.00199481	0.0315187	intron-variant	NCF1	GRCh38.p7	7:74783845	GCAGACGACTGGGGA[A/G]AGTGGGAGGCCAGTG	653361
rs587619899	snp	C/T	0.0217236	0.101931	intron-variant	NCF1	GRCh38.p7	7:74785354	CAGCCCCAGCCAGGA[C/T]GGGGTGTTTAGGGAT	653361
rs587624473	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773395	GCCCAGGAGTTGGAG[C/G]CTGCAGTGAACTGTG	653361
rs587624953	snp	A/G	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74787528	AGGAGACAGAAGGCA[A/G]TTAACATAAAAGAAA	653361
rs587626004	snp	A/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74777448	CTGCAGAACCCAGAA[A/T]CCCCTCCCAGACCAC	653361
rs587629774	snp	A/G	0.0251356	0.109252	intron-variant	NCF1	GRCh38.p7	7:74783649	TGCCCCCTGCCCTCC[A/G]AGGCTGTAGGGGTGT	653361
rs587631811	snp	A/C	0.000541932	0.0164521	missense	NCF1	GRCh38.p7	7:74788699	AGAGCCCCGGGAGCC[A/C]GCTCGGTGAGTGCAG	653361
rs587632076	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773154	GGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG	653361
rs587633477	snp	G/T	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74785747	CATGAGCCGGGTGTG[G/T]TGGTGGGAGCCTGTA	653361
rs587635992	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782689	TGTAGTGAGCTGTGA[C/T]CACGTCACTGTACTC	653361
rs587638476	snp	A/G	0.00119737	0.0244387	intron-variant	NCF1	GRCh38.p7	7:74782874	ACTCAAGATGCCAGC[A/G]CCTGTTCTGGAGGCC	653361
rs587640002	snp	A/G	0.00914312	0.0669923	intron-variant	NCF1	GRCh38.p7	7:74788363	AGGCTGGTGAGGGGC[A/G]TGGAAAACCGCCCAG	653361
rs587640770	snp	C/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74786133	CCAGCTACTCAGGAG[C/G]CTGAGGTGAAAGGAT	653361
rs587641181	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773508	AATGCAATTTGCGAT[A/G]CATCAGTGATAAGTG	653361
rs587641296	snp	C/G	0.000641067	0.017892	missense	NCF1	GRCh38.p7	7:74788604	CCAGCGGTCGCGGAA[C/G]CGCCTCAGCCAGGAC	653361
rs587641317	snp	A/G	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74784665	TCAGGTGATCCGCCC[A/G]CGTTGGCCTCCCAAA	653361
rs587641644	snp	G/T	0.000248756	0.0111497	intron-variant	NCF1	GRCh38.p7	7:74780866	CAGCCGGCGGGGGGG[G/T]GACACCCTGAGGAGA	653361
rs587643499	snp	C/T	0.000560067	0.0167248	intron-variant	NCF1	GRCh38.p7	7:74782910	GGGCCCTGCAATGCC[C/T]ACTCACCCTGCCCTC	653361
rs587643599	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787255	CCAGCCATGACCAAT[A/G]TGGTGAAATCCTGTC	653361
rs587645677	snp	G/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787052	AAAAAAAAAAAAAGA[G/T]CAAAAAACAAACCTA	653361
rs587648376	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74771999	TGATACCCCTTCTCT[A/G]CTAAAAATACAAAAT	653361
rs587650231	snp	G/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785840	GTGAGCCAAGATCGC[G/T]CCATTGCACTCCAGC	653361
rs587651844	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782041	CATCAGCACCTCCAC[A/G]GTTGGATGAAGGGCT	653361
rs587652150	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74784540	TCCTGCCTCAGCCAC[C/T]TGAGTAGCTGGGGTT	653361
rs587652529	snp	A/G	0.0013708	0.0261442	intron-variant	NCF1	GRCh38.p7	7:74783481	TGGCTGCAGGGAGCC[A/G]CTGGGCCCTGCCCCT	653361
rs587653076	snp	A/G	0.00119737	0.0244387	intron-variant	NCF1	GRCh38.p7	7:74787627	CTTGCTATGTTACCC[A/G]GGCTGATCTCCAACT	653361
rs587653999	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74785466	TGAGCCCACCCTTGC[C/T]TGTCTTGTGGGGATC	653361
rs587661330	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74783835	AGGAGGAGGAGCAGA[C/T]GACTGGGGAGAGTGG	653361
rs587662134	snp	A/G	0.0281633	0.115276	intron-variant	NCF1	GRCh38.p7	7:74778319	TAGAGATGGGATTTC[A/G]CTATGTTGCCCAGGC	653361
rs587662513	snp	C/G	5.48913e-05	0.00523857	synonymous-codon	NCF1	GRCh38.p7	7:74779354	GCCCACCAAGATCTC[C/G]CGCTGTCCCCACCTC	653361
rs587663099	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784750	CACTGGGAAGGCCTG[C/T]AGCCCCCAGGCCGAC	653361
rs587665386	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74786484	ACAATCATCGCTCAC[C/T]CAAGCGATCCTCCCA	653361
rs587666154	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74783675	GGTGTGGGAGAAAGG[A/G]GCAGGCAGGGCTCAG	653361
rs587667464	snp	A/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777198	CCAGTGGGTAGTGGG[A/T]TCCTGGGTGCACACA	653361
rs587670140	snp	G/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785358	CCCAGCCAGGACGGG[G/T]TGTTTAGGGATCTGG	653361
rs587670182	snp	A/C	0.00119737	0.0244387	intron-variant	NCF1	GRCh38.p7	7:74783772	TCTCATCGACTCTGG[A/C]TTGGGGGCCCTGGCA	653361
rs587670410	in-del	-/G	0.00060957	0.0174475	intron-variant	NCF1	GRCh38.p7	7:74779456	CTGCCAGGTGGGAGA[-/G]GGAAGGAGGGGTGGG	653361
rs587671809	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74776949	ACTCTTGGACTCAAG[C/T]GATCTTCCCACCTCG	653361
rs587672878	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74775969	TTTTTTTTTATGAGA[C/T]GGAGTCTTACTCTGT	653361
rs587674298	snp	A/G	9.96463e-05	0.00705785	intron-variant	NCF1	GRCh38.p7	7:74783178	CCGGCTCTGTTAGGG[A/G]CCCTAAATGTCCTCC	653361
rs587674714	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782827	CGAAGCCTGGAGAAC[A/G]CTATGCGCCCAGGAA	653361
rs587675858	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772370	CATGACCTTGAATGA[A/G]CTCCAAAAGCTCTGG	653361
rs587678620	snp	A/C	0.0023933	0.0345097	intron-variant	NCF1	GRCh38.p7	7:74787135	TATCCCAGAGTAAAA[A/C]CTGAAACTAAAAACC	653361
rs587679141	snp	A/C	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777479	AGTTAAAGGGGATTT[A/C]TTTATTTATATAAAT	653361
rs587680541	in-del	-/C	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74781289	GGGTCTTTGGAAGGT[-/C]CCTGGAGACTGAAAG	653361
rs587680627	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772151	TTGGGCAACAAGAGC[A/G]AAACTTCGCTTCAAA	653361
rs587682397	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74775791	CAGACTGGAGTGCAG[C/T]GGTGCAATCTCGGCT	653361
rs587683486	snp	C/G	0.0125296	0.0781525	intron-variant	NCF1	GRCh38.p7	7:74783337	TGAAGTGGGCTCAGA[C/G]CTGTGATTCTGTGAG	653361
rs587685954	snp	A/G	0.000399281	0.0141238	missense	NCF1	GRCh38.p7	7:74787988	CTCTGTTGCAGGAAA[A/G]ACGACGTCACAGGCT	653361
rs587686615	snp	C/T	0.00119737	0.0244387	intron-variant	NCF1	GRCh38.p7	7:74782307	AGCCAGGTGTGGTGG[C/T]GGGTGCTTGTAGTCC	653361
rs587688058	snp	C/T	0.0023933	0.0345097	intron-variant	NCF1	GRCh38.p7	7:74787561	TTGGCAAATATAATC[C/T]GCCAATGTCTTCTTT	653361
rs587688879	snp	C/G	0.000109872	0.00741107	intron-variant	NCF1	GRCh38.p7	7:74788716	CTCGGTGAGTGCAGC[C/G]GGAGAGGGCAGGAAG	653361
rs587691787	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773258	CCAGTAGTTTGAGAC[C/T]ATCCTGGGCAACATA	653361
rs587692394	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785815	TTCAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	653361
rs587693328	snp	A/C	3.34185e-05	0.00408756	missense	NCF1	GRCh38.p7	7:74783545	TGGTTCTGTCAGATG[A/C]AAGCAAAGCGAGGCT	653361
rs587695222	snp	G/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74781096	TACTAAAAATCCAAA[G/T]TAGCCAGGCGTGGTG	653361
rs587695598	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787400	AGTCGACATCATGCC[A/G]TTGCACTCCAGCCTA	653361
rs587697744	snp	A/G	0.00237248	0.03436	intron-variant	NCF1	GRCh38.p7	7:74783476	CCTGATGGCTGCAGG[A/G]AGCCGCTGGGCCCTG	653361
rs587697982	snp	A/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784054	TACCATTTTATTTTA[A/T]TATTTATTTATTTAT	653361
rs587698529	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784404	TGATTTCACCCTTTT[A/G]TGTGGATTTACAGCT	653361
rs587699309	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772112	AGGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC	653361
rs587700704	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782608	GGGTGTGGTGGCATA[C/T]GTCTATGGTCCCAGC	653361
rs587701795	snp	C/T	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74781983	TGGTTAGGACTTCAA[C/T]ATATGAATTTTGAGA	653361
rs587704690	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784666	CAGGTGATCCGCCCG[C/T]GTTGGCCTCCCAAAG	653361
rs587706878	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782911	GGCCCTGCAATGCCC[A/G]CTCACCCTGCCCTCC	653361
rs587709073	snp	C/T	5.07164e-05	0.00503544	intron-variant	NCF1	GRCh38.p7	7:74779436	CAGTGAGTGAACTTT[C/T]CACCCTGCCAGGTGG	653361
rs587711107	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784574	GGCATGCACCACCAC[A/G]CCAGGCTAATTTTTT	653361
rs587711470	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785608	ACATTCCTAGCTAGG[C/T]GCAATGGCTCAGGCC	653361
rs587711972	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74788525	GGGCAGGGGCGCCCT[C/T]GGGCTTTGACGACGC	653361
rs587716074	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74776003	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCCAC	653361
rs587716514	snp	A/T	0.000399281	0.0141238	missense	NCF1	GRCh38.p7	7:74779101	CCTTAAAAGAAATGT[A/T]CCCTATTGAGGCAGG	653361
rs587717510	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777602	TTTGAGAGGTATTTA[A/G]GTTTGCAGTGCAGGG	653361
rs587720481	snp	C/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784830	GCCACCTACTCATGG[C/G]TGATCTCTTGTCATA	653361
rs587720716	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74786191	AGTGAGCTATGACTG[C/T]ACCACTGCACCCCAG	653361
rs587721998	snp	A/G	0.0182019	0.0936463	intron-variant	NCF1	GRCh38.p7	7:74783825	ACAGGGAACCAGGAG[A/G]AGGAGCAGACGACTG	653361
rs587722819	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74786576	TAATTTTTTTGTAGG[A/G]ATGGGGTCTCACTAT	653361
rs587722945	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74778369	TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA	653361
rs587725433	snp	C/T	0.000399281	0.0141238	missense	NCF1	GRCh38.p7	7:74788659	TTTCTGCAGCAGCGA[C/T]GCCGCCAGGCGCGGC	653361
rs587730054	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773039	AGTCTCTAATTAAAA[A/G]AAAAAAAAATTAACC	653361
rs587730414	snp	A/C	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74787029	AACAGATGGATTTCC[A/C]TACTGGAAAAAAAAA	653361
rs587731308	snp	G/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784194	CAGCCTCCCCAAGTA[G/T]CTGGGATTACAAGCA	653361
rs587733352	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777035	ACTTTTATCTCCAAT[C/T]TACAGATGAGTCCAT	653361
rs587733564	snp	C/T	0.000427625	0.0146161	intron-variant	NCF1	GRCh38.p7	7:74783648	GTGCCCCCTGCCCTC[C/T]GAGGCTGTAGGGGTG	653361
rs587735115	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74787443	AAAACTCTGTCTTGG[A/G]GTTGGGCGGGGGAAA	653361
rs587735189	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785386	TGGGGTGACTTGTCC[C/T]TGGGACTCTGGGTAA	653361
rs587739768	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74775899	CCACCATGCCCAGCT[C/T]GCATTTTTTGGTAGA	653361
rs587739881	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772216	ATCTGCCAGACCTCA[A/G]CCCTCACCCCCAGGA	653361
rs587742807	snp	A/C	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74783838	AGGAGGAGCAGACGA[A/C]TGGGGAGAGTGGGAG	653361
rs587746171	snp	C/T	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74783734	GGCTGGTTGCTGGCT[C/T]GGCAGAAAAGTCAGG	653361
rs587746334	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74785838	CAGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA	653361
rs587747270	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773346	CACCCGTAGTCCCAG[C/G]TACTCCAGAGGCTGA	653361
rs587747870	snp	C/T	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74784660	TGACCTCAGGTGATC[C/T]GCCCGCGTTGGCCTC	653361
rs587748583	snp	C/T	0.00159617	0.0282053	intron-variant	NCF1	GRCh38.p7	7:74783480	ATGGCTGCAGGGAGC[C/T]GCTGGGCCCTGCCCC	653361
rs587749538	snp	A/G	0.00119737	0.0244387	intron-variant	NCF1	GRCh38.p7	7:74784661	GACCTCAGGTGATCC[A/G]CCCGCGTTGGCCTCC	653361
rs587749584	snp	C/G	0.0232847	0.105357	upstream-variant-2KB	NCF1	GRCh38.p7	7:74773504	ATTAAATGCAATTTG[C/G]GATGCATCAGTGATA	653361
rs587750876	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784504	TCACTGCAACCTTAG[C/T]CTCCTGGGTTCAAGC	653361
rs587752120	snp	A/C	0.0115144	0.0749975	upstream-variant-2KB	NCF1	GRCh38.p7	7:74772325	GGCTGCAGCAGGCTG[A/C]CTGGGGCTGAGGCCC	653361
rs587753749	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782905	CAGATGGGCCCTGCA[A/G]TGCCCACTCACCCTG	653361
rs587754645	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782639	TATTCGGGAGGCTGA[A/G]GCAGGGAGATTGCTT	653361
rs587755234	snp	C/T	4.97203e-05	0.00498575	missense	NCF1	GRCh38.p7	7:74783584	GCGTCCTTCCTCGAG[C/T]CCCTGGACAGTCCTG	653361
rs587757490	snp	C/T	0.00953873	0.0683987	intron-variant	NCF1	GRCh38.p7	7:74781555	TGTTGTTTTCAGTGA[C/T]AGGGTCTCGCTCTGT	653361
rs587763288	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777489	GATTTATTTATTTAT[A/G]TAAATTTTTGTGACA	653361
rs587763821	snp	C/T	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782873	GACTCAAGATGCCAG[C/T]GCCTGTTCTGGAGGC	653361
rs587766030	snp	A/G	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74786038	ACAAGTTCAAGACCA[A/G]CCTGGGCAATGTAGG	653361
rs587766077	snp	A/C	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74788344	GAGGGGGACGACAGA[A/C]CGAAGGCTGGTGAGG	653361
rs587766712	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74782308	GCCAGGTGTGGTGGC[A/G]GGTGCTTGTAGTCCC	653361
rs587767903	snp	A/G	0.000798403	0.0199641	intron-variant	NCF1	GRCh38.p7	7:74787595	CTTTACTTTTTTCGG[A/G]AGGTAGAGATAGGGG	653361
rs587768074	snp	A/C	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74783076	GGTCAGACCTCCCAC[A/C]TTACGGGGCTCCTTC	653361
rs587768315	snp	A/G/T	0.000271981	0.0116589	intron-variant	NCF1	GRCh38.p7	7:74788731	GGGAGAGGGCAGGAA[A/G/T]GGCAAGCCGTAGAGG	653361
rs587775181	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74777620	TTGCAGTGCAGGGGC[A/G]CAATCATAGCTCACT	653361
rs587775915	snp	A/G	0.000399281	0.0141238	intron-variant	NCF1	GRCh38.p7	7:74784577	ATGCACCACCACGCC[A/G]GGCTAATTTTTTGTA	653361
rs759662302	in-del	-/GACC			intron-variant	NCF1	GRCh38.p7	7:74782088	TCAGGTCCCACAGTG[-/GACC]TACTGAACAGGATAG	653361
rs765321859	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74785730	TCTACTAAAAACACA[A/G]ACATGAGCCGGGTGT	653361
rs776660927	in-del	-/C			upstream-variant-2KB	NCF1	GRCh38.p7	7:74772200	GCATGTCTTGGCTTT[-/C]ATCTGCCAGACCTCA	653361
rs781784127	snp	A/C/G	0.000233136	0.0107945	synonymous-codon	NCF1	GRCh38.p7	7:74783024	GATGGCTCTGTCCAC[A/C/G]GGGGACGTGGTGGAG	653361
rs781786233	in-del	-/AAA	9.65577e-05	0.00694763	intron-variant	NCF1	GRCh38.p7	7:74779072	TCTTCTTGTCTTTTT[-/AAA]AATGTTTAGAAAACC	653361
rs781786929	snp	C/T	1.77685e-05	0.00298059	missense	NCF1	GRCh38.p7	7:74777321	AAGGTGGTCTACCGG[C/T]GCTTCACCGAGATCT	653361
rs781789430	snp	A/G	5.16961e-05	0.00508383	missense	NCF1	GRCh38.p7	7:74779289	GGGCAGCGGGCCGCC[A/G]AGAACCGCCAGGGCA	653361
rs781801935	snp	A/C	0.000191681	0.00978794	intron-variant	NCF1	GRCh38.p7	7:74783365	GAGCATGTGTGCATG[A/C]ATGCATGTGACCTCA	653361
rs781804912	snp	A/C	0.00108345	0.0232497	intron-variant	NCF1	GRCh38.p7	7:74783111	GGTGCTCAGGAACCC[A/C]CAGCCACAAGCCCCC	653361
rs781805772	snp	A/G	0.000323782	0.0127195	intron-variant	NCF1	GRCh38.p7	7:74780850	GGTGAGAGGACGGGG[A/G]GCAGCCGGCGGGGGG	653361
rs781808663	snp	C/G	0.000149065	0.00863192	synonymous-codon	NCF1	GRCh38.p7	7:74788640	TCGCCGCAACAGCGT[C/G]CGTTTTCTGCAGCAG	653361
rs781808976	snp	A/C/T	0.000169262	0.00919795	intron-variant	NCF1	GRCh38.p7	7:74779056	ACAAATATTCCTTCA[A/C/T]GTCTTCTTGTCTTTT	653361
rs781817519	snp	A/C	2.46996e-05	0.00351414	intron-variant	NCF1	GRCh38.p7	7:74777393	CCCACCGTTCCAGCT[A/C]CACCCTTTGGGAAGG	653361
rs781821575	snp	A/G	5.45976e-05	0.00522454	intron-variant	NCF1	GRCh38.p7	7:74777235	CCTCTTTGGAGGCTG[A/G]ATGGGGTCCCCCGAC	653361
rs781834627	snp	A/G	0.000573394	0.0169224	intron-variant	NCF1	GRCh38.p7	7:74783267	TGCTTGGCAGGCCGG[A/G]GCGGGGCATGTCTGC	653361
rs781835731	snp	C/T	1.90065e-05	0.00308268	missense	NCF1	GRCh38.p7	7:74777345	GAGATCTACGAGTTC[C/T]ATGTGAGTGTGGGGA	653361
rs781840733	snp	A/T	1.9319e-05	0.00310791	intron-variant	NCF1	GRCh38.p7	7:74779214	GGGGCTCACCTGCCC[A/T]CCCAGCCCCTCTCGG	653361
rs781849042	snp	C/G	0.000334201	0.0129224	intron-variant	NCF1	GRCh38.p7	7:74783145	CAAGGCTCAGGCAGC[C/G]TTGCCCCTGGGAGGA	653361
rs781857646	snp	A/G	4.57195e-05	0.00478097	missense	NCF1	GRCh38.p7	7:74788663	TGCAGCAGCGACGCC[A/G]CCAGGCGCGGCCGGG	653361
rs781859571	snp	C/T	3.3211e-05	0.00407485	synonymous-codon	NCF1	GRCh38.p7	7:74783030	TCTGTCCACGGGGGA[C/T]GTGGTGGAGGTCGTA	653361
rs781862114	snp	C/T	1.75096e-05	0.0029588	missense	NCF1	GRCh38.p7	7:74779367	TCCCGCTGTCCCCAC[C/T]TCCTCGACTTCTTCA	653361
rs781890686	snp	C/T	0.000353045	0.0132815	intron-variant	NCF1	GRCh38.p7	7:74783301	TTCTGTCTGGATGGG[C/T]ATGGGACCGTCTGTT	653361
rs781894224	snp	A/G	3.67803e-05	0.00428821	intron-variant	NCF1	GRCh38.p7	7:74783105	TCCCCTGGTGCTCAG[A/G]AACCCACAGCCACAA	653361
rs781894954	snp	A/G	0.0129305	0.0793602	intron-variant	NCF1	GRCh38.p7	7:74780116	GCGGGGGAAGGATGG[A/G]CTCTGCAGTGGGGTC	653361
rs781909474	snp	A/G	1.7174e-05	0.00293031	missense	NCF1	GRCh38.p7	7:74783611	CCTGACGAGACGGAA[A/G]ACCCTGAGCCCAACT	653361
rs781915784	snp	C/T	6.62427e-05	0.00575473	synonymous-codon	NCF1	GRCh38.p7	7:74783580	CCCAGCGTCCTTCCT[C/T]GAGCCCCTGGACAGT	653361
rs781921509	snp	G/T	0.000373134	0.0136539	intron-variant	NCF1	GRCh38.p7	7:74783253	GCTGTGGGCATCTGT[G/T]CTTGGCAGGCCGGGG	653361
rs781933814	snp	C/T	0.000185839	0.00963769	intron-variant	NCF1	GRCh38.p7	7:74779176	AGCACGGGGCTGAGC[C/T]GCCTGTCAGGGGGTC	653361
rs781945357	snp	A/C	1.75977e-05	0.00296624	missense	NCF1	GRCh38.p7	7:74788574	GTCGTCCATCCGCAA[A/C]GCGCACAGCATCCAC	653361
rs781953146	snp	C/T	3.89241e-05	0.00441141	missense	NCF1	GRCh38.p7	7:74779344	TCATGAGCCTGCCCA[C/T]CAAGATCTCCCGCTG	653361
rs781954000	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74781635	CCTCCTGGGCTGAAG[C/T]GATCCTCCCACCTCA	653361
rs781959708	snp	A/G	5.07335e-05	0.00503629	missense	NCF1	GRCh38.p7	7:74777295	TGGTGAAATGGCAGG[A/G]CCTGTCGGAGAAGGT	653361
rs781959928	snp	A/G/T	3.48221e-05	0.00417254	stop-gained, missense	NCF1	GRCh38.p7	7:74783531	CTGGCACAGGTTGGT[A/G/T]GTTCTGTCAGATGAA	653361
rs781974943	snp	C/G	2.71846e-05	0.00368668	intron-variant	NCF1	GRCh38.p7	7:74783094	ACGGGGCTCCTTCCC[C/G]TGGTGCTCAGGAACC	653361
rs781980620	snp	C/T	0.16943	0.236661	intron-variant	NCF1	GRCh38.p7	7:74779197	TCAGGGGGTCATTGG[C/T]GGGGGCTCACCTGCC	653361
rs781983704	snp	C/G	8.7634e-05	0.00661886	missense	NCF1	GRCh38.p7	7:74779394	TTCAAGGTGCGCCCT[C/G]ATGACCTCAAGCTCC	653361
rs781996787	snp	C/T	1.67897e-05	0.00289733	synonymous-codon	NCF1	GRCh38.p7	7:74783016	GGCTCCGAGATGGCT[C/T]TGTCCACGGGGGACG	653361
rs782002877	snp	A/G	1.72534e-05	0.00293708	missense	NCF1	GRCh38.p7	7:74779286	GACGGGCAGCGGGCC[A/G]CCGAGAACCGCCAGG	653361
rs782009050	snp	C/T	0.000131744	0.00811508	intron-variant	NCF1	GRCh38.p7	7:74783207	CCCCACACTGTGGGT[C/T]GCCTTCTGTCTTAGT	653361
rs782022363	snp	C/T	1.75943e-05	0.00296595	synonymous-codon	NCF1	GRCh38.p7	7:74788583	CCGCAACGCGCACAG[C/T]ATCCACCAGCGGTCG	653361
rs782028515	snp	C/T	0.000105158	0.00725038	intron-variant	NCF1	GRCh38.p7	7:74788136	GAGCGGGGCGCACCA[C/T]GGGTTCGCTCTGTCT	653361
rs782028894	snp	A/C	1.88831e-05	0.00307265	intron-variant	NCF1	GRCh38.p7	7:74783072	GAGCGGTCAGACCTC[A/C]CACCTTACGGGGCTC	653361
rs782029909	snp	C/T	5.54595e-05	0.00526561	missense	NCF1	GRCh38.p7	7:74779413	ACCTCAAGCTCCCCA[C/T]GGACAACCAGTGAGT	653361
rs782032278	snp	C/T	2.15492e-05	0.0032824	synonymous-codon	NCF1	GRCh38.p7	7:74779330	GTACTGCGGCACGCT[C/T]ATGAGCCTGCCCACC	653361
rs782034034	snp	A/G	2.13481e-05	0.00326705	intron-variant	NCF1	GRCh38.p7	7:74777370	TGGGGACGGAGGAGG[A/G]ACAGGGACCCACCGT	653361
rs782037135	snp	C/T	0.000304074	0.0123266	missense	NCF1	GRCh38.p7	7:74782999	ACTACGAGAAGACCT[C/T]GGGCTCCGAGATGGC	653361
rs782039216	snp	A/G	1.66966e-05	0.00288929	missense	NCF1	GRCh38.p7	7:74777273	TTCCCCCAGGTGTAC[A/G]TGTTCCTGGTGAAAT	653361
rs782039400	snp	C/T	0.00021077	0.0102636	intron-variant	NCF1	GRCh38.p7	7:74783080	AGACCTCCCACCTTA[C/T]GGGGCTCCTTCCCCT	653361
rs782052125	snp	C/T	3.33968e-05	0.00408623	missense	NCF1	GRCh38.p7	7:74777274	TCCCCCAGGTGTACA[C/T]GTTCCTGGTGAAATG	653361
rs782067165	snp	A/G	0.00117578	0.0242179	synonymous-codon	NCF1	GRCh38.p7	7:74782967	CATCATCCTGCAGAC[A/G]TACCGCGCCATTGCC	653361
rs782067600	snp	A/G	3.72384e-05	0.00431484	intron-variant	NCF1	GRCh38.p7	7:74788730	CGGGAGAGGGCAGGA[A/G]GGGCAAGCCGTAGAG	653361
rs782073447	snp	G/T	2.62505e-05	0.00362278	intron-variant	NCF1	GRCh38.p7	7:74779202	GGGTCATTGGCGGGG[G/T]CTCACCTGCCCTCCC	653361
rs782074398	snp	A/G	0.000278316	0.0117932	synonymous-codon	NCF1	GRCh38.p7	7:74779414	CCTCAAGCTCCCCAC[A/G]GACAACCAGTGAGTG	653361
rs782077045	snp	A/G	0.000351556	0.0132535	intron-variant	NCF1	GRCh38.p7	7:74779177	GCACGGGGCTGAGCC[A/G]CCTGTCAGGGGGTCA	653361
rs782091728	snp	G/T	2.53379e-05	0.00355926	intron-variant	NCF1	GRCh38.p7	7:74777399	GTTCCAGCTCCACCC[G/T]TTGGGAAGGACCTTA	653361
rs782100556	snp	A/G	5.14178e-05	0.00507014	missense	NCF1	GRCh38.p7	7:74783007	AAGACCTCGGGCTCC[A/G]AGATGGCTCTGTCCA	653361
rs782104553	snp	A/G	1.7208e-05	0.00293321	synonymous-codon	NCF1	GRCh38.p7	7:74779282	GTTTGACGGGCAGCG[A/G]GCCGCCGAGAACCGC	653361
rs782109262	snp	A/G	0.000329218	0.0128258	intron-variant	NCF1	GRCh38.p7	7:74783283	GCGGGGCATGTCTGC[A/G]TGTTCTGTCTGGATG	653361
rs782113541	snp	A/G	0.000184281	0.00959721	intron-variant	NCF1	GRCh38.p7	7:74788733	GAGAGGGCAGGAAGG[A/G]CAAGCCGTAGAGGCG	653361
rs782119877	snp	A/C/G/T	0.00018768	0.00968564	intron-variant	NCF1	GRCh38.p7	7:74779198	CAGGGGGTCATTGGC[A/C/G/T]GGGGCTCACCTGCCC	653361
rs782126215	snp	A/G	3.05535e-05	0.00390843	intron-variant	NCF1	GRCh38.p7	7:74783099	GCTCCTTCCCCTGGT[A/G]CTCAGGAACCCACAG	653361
rs782128694	snp	A/G	1.7938e-05	0.00299478	missense	NCF1	GRCh38.p7	7:74779404	GCCCTGATGACCTCA[A/G]GCTCCCCACGGACAA	653361
rs782133512	snp	A/C			intron-variant	NCF1	GRCh38.p7	7:74782051	TCCACGGTTGGATGA[A/C]GGGCTGGTCAGAAAT	653361
rs782142500	snp	A/G/T	6.63244e-05	0.00575833	missense	NCF1	GRCh38.p7	7:74783555	AGATGAAAGCAAAGC[A/G/T]AGGCTGGATCCCAGC	653361
rs782144307	snp	C/G/T	8.62023e-05	0.00656465	synonymous-codon	NCF1	GRCh38.p7	7:74779288	CGGGCAGCGGGCCGC[C/G/T]GAGAACCGCCAGGGC	653361
rs782157090	snp	A/G	0.00118851	0.0243484	intron-variant	NCF1	GRCh38.p7	7:74783208	CCCACACTGTGGGTC[A/G]CCTTCTGTCTTAGTG	653361
rs782162649	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74775471	TATTTGAGAGTGAGT[C/T]GAAGACGTGTTTCTT	653361
rs782166417	snp	C/G	5.45549e-05	0.0052225	intron-variant	NCF1	GRCh38.p7	7:74788755	GTAGAGGCGGAGTCA[C/G]CGGGAGAGGCGGGGC	653361
rs782169559	snp	A/G	0.00259403	0.0359205	intron-variant	NCF1	GRCh38.p7	7:74788139	CGGGGCGCACCACGG[A/G]TTCGCTCTGTCTAGG	653361
rs782170312	snp	A/C	4.31118e-05	0.00464263	intron-variant	NCF1	GRCh38.p7	7:74783107	CCCTGGTGCTCAGGA[A/C]CCCACAGCCACAAGC	653361
rs782176450	snp	A/G	1.7731e-05	0.00297744	synonymous-codon	NCF1	GRCh38.p7	7:74783000	CTACGAGAAGACCTC[A/G]GGCTCCGAGATGGCT	653361
rs782183721	snp	C/T	1.72039e-05	0.00293285	stop-gained	NCF1	GRCh38.p7	7:74779277	AAGTGGTTTGACGGG[C/T]AGCGGGCCGCCGAGA	653361
rs782191766	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74776011	GAGTGCAATGGCACA[A/G]TCTCCACTCACTGCA	653361
rs782193656	snp	C/T	1.68292e-05	0.00290075	intron-variant	NCF1	GRCh38.p7	7:74777259	CCCCGACTCTGGCTT[C/T]CCCCCAGGTGTACAT	653361
rs782197230	snp	A/T	5.17674e-05	0.00508734	intron-variant	NCF1	GRCh38.p7	7:74779243	GGGCTTGACCTCATG[A/T]TCTCTGGTGCCAGCT	653361
rs782200934	snp	C/G	6.0045e-05	0.00547895	missense	NCF1	GRCh38.p7	7:74788698	CAGAGCCCCGGGAGC[C/G]CGCTCGGTGAGTGCA	653361
rs782205505	snp	A/G/T	0.000104623	0.007232	missense	NCF1	GRCh38.p7	7:74779389	ACTTCTTCAAGGTGC[A/G/T]CCCTGATGACCTCAA	653361
rs782208737	snp	A/G	1.6476e-05	0.00287014	missense	NCF1	GRCh38.p7	7:74783055	GTCGTAGAGAAGAGC[A/G]AGAGCGGTCAGACCT	653361
rs782209678	in-del	-/C	9.20556e-05	0.00678375	intron-variant	NCF1	GRCh38.p7	7:74783122	ACCCACAGCCACAAG[-/C]CCCCTGCCAAGGCTC	653361
rs782214627	snp	A/G/T	6.19308e-05	0.00556437	intron-variant	NCF1	GRCh38.p7	7:74777362	TGTGAGTGTGGGGAC[A/G/T]GAGGAGGGACAGGGA	653361
rs782219576	snp	C/T	0.00034632	0.0131545	intron-variant	NCF1	GRCh38.p7	7:74783637	CAACTATGCAGGTGC[C/T]CCCTGCCCTCCGAGG	653361
rs782223128	in-del	-/A			intron-variant	NCF1	GRCh38.p7	7:74786237	AAGACCCTGTCTCAA[-/A]AAAAAAAAAAAAAAA	653361
rs782223424	snp	C/T	2.192e-05	0.00331051	missense	NCF1	GRCh38.p7	7:74782986	CGCGCCATTGCCAAC[C/T]ACGAGAAGACCTCGG	653361
rs782232664	snp	C/T	8.44844e-05	0.00649885	intron-variant	NCF1	GRCh38.p7	7:74783170	GGAGGACTCCGGCTC[C/T]GTTAGGGGCCCTAAA	653361
rs782234231	snp	C/T	1.71773e-05	0.00293059	missense	NCF1	GRCh38.p7	7:74779269	CAGCTCCCAAGTGGT[C/T]TGACGGGCAGCGGGC	653361
rs782236954	snp	A/C/G/T	0.000241904	0.0109957	intron-variant	NCF1	GRCh38.p7	7:74780861	GGGGGCAGCCGGCGG[A/C/G/T]GGGGGGACACCCTGA	653361
rs782242537	snp	C/T	0.000196239	0.00990358	synonymous-codon	NCF1	GRCh38.p7	7:74779135	GATCAATCCAGAGAA[C/T]AGGATCATCCCCCAC	653361
rs782260476	snp	A/C	1.78014e-05	0.00298335	intron-variant	NCF1	GRCh38.p7	7:74783068	GCGAGAGCGGTCAGA[A/C]CTCCCACCTTACGGG	653361
rs782264937	snp	A/G	1.85858e-05	0.00304837	synonymous-codon	NCF1	GRCh38.p7	7:74782994	TGCCAACTACGAGAA[A/G]ACCTCGGGCTCCGAG	653361
rs782272331	snp	C/G	1.67144e-05	0.00289084	missense	NCF1	GRCh38.p7	7:74777267	CTGGCTTTCCCCCAG[C/G]TGTACATGTTCCTGG	653361
rs782280189	in-del	-/A			intron-variant	NCF1	GRCh38.p7	7:74787035	GGATTTCCATACTGG[-/A]AAAAAAAAAAAAAAG	653361
rs782284699	snp	A/G	3.90656e-05	0.00441942	missense	NCF1	GRCh38.p7	7:74788704	CCCGGGAGCCCGCTC[A/G]GTGAGTGCAGCGGGA	653361
rs782289015	snp	C/T	6.45432e-05	0.00568044	intron-variant	NCF1	GRCh38.p7	7:74783161	TTGCCCCTGGGAGGA[C/T]TCCGGCTCTGTTAGG	653361
rs782289802	snp	C/T	0.000148049	0.00860249	synonymous-codon	NCF1	GRCh38.p7	7:74788688	GCCGGGACCGCAGAG[C/T]CCCGGGAGCCCGCTC	653361
rs782295551	snp	A/G	0.001372	0.0261556	intron-variant	NCF1	GRCh38.p7	7:74779166	CTCCCAGGTGAGCAC[A/G]GGGCTGAGCCGCCTG	653361
rs782297857	snp	C/T	5.2054e-05	0.0051014	synonymous-codon	NCF1	GRCh38.p7	7:74779375	TCCCCACCTCCTCGA[C/T]TTCTTCAAGGTGCGC	653361
rs782302035	snp	A/G	3.84549e-05	0.00438474	intron-variant	NCF1	GRCh38.p7	7:74777351	TACGAGTTCCATGTG[A/G]GTGTGGGGACGGAGG	653361
rs782306577	snp	C/T	5.20793e-05	0.00510264	missense	NCF1	GRCh38.p7	7:74779377	CCCACCTCCTCGACT[C/T]CTTCAAGGTGCGCCC	653361
rs782308134	snp	C/T	0.000142572	0.0084419	intron-variant	NCF1	GRCh38.p7	7:74783164	CCCCTGGGAGGACTC[C/T]GGCTCTGTTAGGGGC	653361
rs782310642	snp	C/T	0.000110675	0.00743808	intron-variant	NCF1	GRCh38.p7	7:74779171	AGGTGAGCACGGGGC[C/T]GAGCCGCCTGTCAGG	653361
rs782313991	snp	G/T	0.000287274	0.0119814	missense	NCF1	GRCh38.p7	7:74788559	GTCCCGCTGGGCCAG[G/T]TCGTCCATCCGCAAC	653361
rs782329551	snp	C/T	1.74558e-05	0.00295425	synonymous-codon	NCF1	GRCh38.p7	7:74783003	CGAGAAGACCTCGGG[C/T]TCCGAGATGGCTCTG	653361
rs782331439	snp	C/T	3.44459e-05	0.00414991	missense	NCF1	GRCh38.p7	7:74779280	TGGTTTGACGGGCAG[C/T]GGGCCGCCGAGAACC	653361
rs782335665	snp	C/T	1.6752e-05	0.00289408	intron-variant	NCF1	GRCh38.p7	7:74777263	GACTCTGGCTTTCCC[C/T]CAGGTGTACATGTTC	653361
rs782343851	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74782462	AAAAGTTGGGAAAAG[A/G]CCAGGTGCAGTGGCT	653361
rs782348351	snp	C/G	0.000232639	0.0107826	intron-variant	NCF1	GRCh38.p7	7:74779187	GAGCCGCCTGTCAGG[C/G]GGTCATTGGCGGGGG	653361
rs782364575	snp	A/G	2.24002e-05	0.00334658	missense	NCF1	GRCh38.p7	7:74779323	TTACCGAGTACTGCG[A/G]CACGCTCATGAGCCT	653361
rs782366860	snp	C/G	1.67995e-05	0.00289819	missense	NCF1	GRCh38.p7	7:74783541	TTGGTGGTTCTGTCA[C/G]ATGAAAGCAAAGCGA	653361
rs782384491	snp	A/C/T	0.00114761	0.0239319	intron-variant	NCF1	GRCh38.p7	7:74782908	ATGGGCCCTGCAATG[A/C/T]CCACTCACCCTGCCC	653361
rs782386704	snp	C/T	6.88065e-05	0.00586503	synonymous-codon	NCF1	GRCh38.p7	7:74779273	TCCCAAGTGGTTTGA[C/T]GGGCAGCGGGCCGCC	653361
rs782395518	snp	C/G	0.00428264	0.0460758	missense	NCF1	GRCh38.p7	7:74779138	CAATCCAGAGAACAG[C/G]ATCATCCCCCACCTC	653361
rs782401143	snp	C/T	1.8683e-05	0.00305633	intron-variant	NCF1	GRCh38.p7	7:74783071	AGAGCGGTCAGACCT[C/T]CCACCTTACGGGGCT	653361
rs782402177	snp	A/C	3.69385e-05	0.00429743	synonymous-codon	NCF1	GRCh38.p7	7:74779411	TGACCTCAAGCTCCC[A/C]ACGGACAACCAGTGA	653361
rs782404949	snp	C/T	7.25466e-05	0.00602229	synonymous-codon	NCF1	GRCh38.p7	7:74782997	CAACTACGAGAAGAC[C/T]TCGGGCTCCGAGATG	653361
rs782407343	snp	G/T	2.12623e-05	0.00326048	intron-variant	NCF1	GRCh38.p7	7:74777369	GTGGGGACGGAGGAG[G/T]GACAGGGACCCACCG	653361
rs782408014	snp	A/G	1.67019e-05	0.00288975	synonymous-codon	NCF1	GRCh38.p7	7:74777269	GGCTTTCCCCCAGGT[A/G]TACATGTTCCTGGTG	653361
rs782417498	snp	G/T	0.00186741	0.0304995	intron-variant	NCF1	GRCh38.p7	7:74785154	GGGCCGACCTCACAC[G/T]GTGCTCTGTGCCCCT	653361
rs782419776	snp	A/C	8.68961e-05	0.00659094	missense	NCF1	GRCh38.p7	7:74779328	GAGTACTGCGGCACG[A/C]TCATGAGCCTGCCCA	653361
rs782424535	snp	C/G	0.000212404	0.0103033	intron-variant	NCF1	GRCh38.p7	7:74783251	TGGCTGTGGGCATCT[C/G]TGCTTGGCAGGCCGG	653361
rs782425656	snp	C/T	0.0005997	0.0173058	intron-variant	NCF1	GRCh38.p7	7:74783487	CAGGGAGCCGCTGGG[C/T]CCTGCCCCTCAGTCA	653361
rs782427361	snp	A/C	0.000355387	0.0133254	intron-variant	NCF1	GRCh38.p7	7:74788713	CCGCTCGGTGAGTGC[A/C]GCGGGAGAGGGCAGG	653361
rs782430982	snp	G/T	0.000141874	0.00842122	missense	NCF1	GRCh38.p7	7:74788692	GGACCGCAGAGCCCC[G/T]GGAGCCCGCTCGGTG	653361
rs782434810	snp	A/C	1.72044e-05	0.0029329	missense	NCF1	GRCh38.p7	7:74783612	CTGACGAGACGGAAG[A/C]CCCTGAGCCCAACTA	653361
rs782438868	snp	C/T	6.68412e-05	0.00578067	synonymous-codon	NCF1	GRCh38.p7	7:74779321	ACTTACCGAGTACTG[C/T]GGCACGCTCATGAGC	653361
rs782442373	snp	C/T	3.71464e-05	0.0043095	synonymous-codon	NCF1	GRCh38.p7	7:74777329	CTACCGGCGCTTCAC[C/T]GAGATCTACGAGTTC	653361
rs782450062	snp	A/G	1.65869e-05	0.00287979	missense	NCF1	GRCh38.p7	7:74783040	GGGGACGTGGTGGAG[A/G]TCGTAGAGAAGAGCG	653361
rs782453617	snp	A/G	1.72409e-05	0.00293601	missense	NCF1	GRCh38.p7	7:74779292	CAGCGGGCCGCCGAG[A/G]ACCGCCAGGGCACAC	653361
rs782465451	snp	A/G	1.66504e-05	0.0028853	intron-variant	NCF1	GRCh38.p7	7:74783128	AGCCACAAGCCCCCT[A/G]CCAAGGCTCAGGCAG	653361
rs782481752	snp	C/G	0.000154955	0.00880076	missense	NCF1	GRCh38.p7	7:74788650	AGCGTCCGTTTTCTG[C/G]AGCAGCGACGCCGCC	653361
rs782485806	snp	A/C/T	7.05671e-05	0.00593964	missense	NCF1	GRCh38.p7	7:74779364	ATCTCCCGCTGTCCC[A/C/T]ACCTCCTCGACTTCT	653361
rs782492205	snp	C/T	0.000220629	0.0105007	intron-variant	NCF1	GRCh38.p7	7:74783640	CTATGCAGGTGCCCC[C/T]TGCCCTCCGAGGCTG	653361
rs782495977	snp	A/C	1.90228e-05	0.003084	missense	NCF1	GRCh38.p7	7:74777346	AGATCTACGAGTTCC[A/C]TGTGAGTGTGGGGAC	653361
rs782496561	snp	C/T	2.07557e-05	0.0032214	synonymous-codon	NCF1	GRCh38.p7	7:74782988	CGCCATTGCCAACTA[C/T]GAGAAGACCTCGGGC	653361
rs782509047	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74785680	GTGAGGTCAGGAGTT[C/T]GAGACCACCCTGGCC	653361
rs782512803	in-del	-/G			intron-variant	NCF1	GRCh38.p7	7:74780859	CGGGGGGCAGCCGGC[-/G]GGGGGGGGGACACCC	653361
rs782515324	snp	C/G	1.78302e-05	0.00298577	intron-variant	NCF1	GRCh38.p7	7:74779223	CTGCCCTCCCAGCCC[C/G]TCTCGGGCTTGACCT	653361
rs782515532	in-del	-/A			intron-variant	NCF1	GRCh38.p7	7:74775525	GCATTTCTTAAAATC[-/A]AGGCATTCTCTTACA	653361
rs782518527	snp	A/C/G	0.000116734	0.00763893	intron-variant	NCF1	GRCh38.p7	7:74783156	CAGCCTTGCCCCTGG[A/C/G]AGGACTCCGGCTCTG	653361
rs782518889	snp	A/C	2.24676e-05	0.00335161	synonymous-codon	NCF1	GRCh38.p7	7:74788671	CGACGCCGCCAGGCG[A/C]GGCCGGGACCGCAGA	653361
rs782521032	snp	A/G	0.000413034	0.0143648	intron-variant	NCF1	GRCh38.p7	7:74777239	TTTGGAGGCTGAATG[A/G]GGTCCCCCGACTCTG	653361
rs782526868	snp	A/G	8.29855e-05	0.00644095	missense	NCF1	GRCh38.p7	7:74783031	CTGTCCACGGGGGAC[A/G]TGGTGGAGGTCGTAG	653361
rs782543009	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74785470	CCCACCCTTGCCTGT[C/T]TTGTGGGGATCCAAT	653361
rs782544408	snp	A/G	5.15894e-05	0.00507859	missense	NCF1	GRCh38.p7	7:74777309	GACCTGTCGGAGAAG[A/G]TGGTCTACCGGCGCT	653361
rs782546882	snp	C/T	0.000135602	0.00823303	intron-variant	NCF1	GRCh38.p7	7:74783308	TGGATGGGTATGGGA[C/T]CGTCTGTTCATTATG	653361
rs782552650	snp	A/G	0.000473821	0.0153846	intron-variant	NCF1	GRCh38.p7	7:74780763	CAAGGGTCTCACCCA[A/G]ACTGTTCTCTCCTCA	653361
rs782553526	snp	C/G/T	3.47556e-05	0.00416855	intron-variant	NCF1	GRCh38.p7	7:74779233	AGCCCCTCTCGGGCT[C/G/T]GACCTCATGTTCTCT	653361
rs782555266	snp	A/G	0.00059288	0.0172072	missense	NCF1	GRCh38.p7	7:74782983	TACCGCGCCATTGCC[A/G]ACTACGAGAAGACCT	653361
rs782557413	in-del	-/C	4.08438e-05	0.00451888	intron-variant	NCF1	GRCh38.p7	7:74779197	TCAGGGGGTCATTGG[-/C]GGGGGCTCACCTGCC	653361
rs782558908	snp	A/T	0.000268132	0.0115756	intron-variant	NCF1	GRCh38.p7	7:74778362	CCTGGACTCAAGTGA[A/T]CCTCCCGCCTCAGCC	653361
rs782563385	snp	C/G	4.58043e-05	0.0047854	missense	NCF1	GRCh38.p7	7:74782985	CCGCGCCATTGCCAA[C/G]TACGAGAAGACCTCG	653361
rs782570759	snp	C/G	0.020218	0.0984897	intron-variant	NCF1	GRCh38.p7	7:74780846	GACAGGTGAGAGGAC[C/G]GGGGGCAGCCGGCGG	653361
rs782572273	snp	A/G	0.00126723	0.0251398	intron-variant	NCF1	GRCh38.p7	7:74783166	CCTGGGAGGACTCCG[A/G]CTCTGTTAGGGGCCC	653361
rs782574958	snp	C/G	0.000297663	0.012196	intron-variant	NCF1	GRCh38.p7	7:74778436	CAACCTGAGTTTTAA[C/G]AGGATCCCTTTGGCG	653361
rs782580709	snp	A/G	1.69522e-05	0.00291132	intron-variant	NCF1	GRCh38.p7	7:74777254	GGGTCCCCCGACTCT[A/G]GCTTTCCCCCAGGTG	653361
rs782586627	snp	A/C	1.7544e-05	0.00296171	missense	NCF1	GRCh38.p7	7:74783618	AGACGGAAGACCCTG[A/C]GCCCAACTATGCAGG	653361
rs782588016	snp	A/G	2.02636e-05	0.00318299	synonymous-codon	NCF1	GRCh38.p7	7:74788694	ACCGCAGAGCCCCGG[A/G]AGCCCGCTCGGTGAG	653361
rs782593576	snp	A/C	1.73866e-05	0.00294839	missense	NCF1	GRCh38.p7	7:74779382	CTCCTCGACTTCTTC[A/C]AGGTGCGCCCTGATG	653361
rs782597081	snp	C/T	5.64743e-05	0.00531356	synonymous-codon	NCF1	GRCh38.p7	7:74777338	CTTCACCGAGATCTA[C/T]GAGTTCCATGTGAGT	653361
rs782608402	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74787170	GGGGCTGGACAGGGA[A/G]CTCACGCCTGTAATC	653361
rs782619739	snp	A/G	0.000515872	0.0160521	missense	NCF1	GRCh38.p7	7:74779263	TGGTGCCAGCTCCCA[A/G]GTGGTTTGACGGGCA	653361
rs782625469	snp	A/G	4.61563e-05	0.00480375	intron-variant	NCF1	GRCh38.p7	7:74783134	AAGCCCCCTGCCAAG[A/G]CTCAGGCAGCCTTGC	653361
rs782626961	in-del	-/GG	0.000830289	0.0203582	intron-variant	NCF1	GRCh38.p7	7:74780860	CGGGGGGCAGCCGGC[-/GG]GGGGGGGACACCCTG	653361
rs782629025	snp	A/G	0.000605144	0.0173841	synonymous-codon	NCF1	GRCh38.p7	7:74779132	GGCGATCAATCCAGA[A/G]AACAGGATCATCCCC	653361
rs782635646	snp	C/T	4.36939e-05	0.00467387	synonymous-codon	NCF1	GRCh38.p7	7:74779312	CCAGGGCACACTTAC[C/T]GAGTACTGCGGCACG	653361
rs782643879	snp	A/G	5.34574e-05	0.0051697	intron-variant	NCF1	GRCh38.p7	7:74777241	TGGAGGCTGAATGGG[A/G]TCCCCCGACTCTGGC	653361
rs782656910	snp	C/G	0.000132529	0.00813923	synonymous-codon	NCF1	GRCh38.p7	7:74788703	CCCCGGGAGCCCGCT[C/G]GGTGAGTGCAGCGGG	653361
rs782657204	snp	C/T			intron-variant	NCF1	GRCh38.p7	7:74781580	CTCTGTTGCCCAGGC[C/T]AGAGTGAAGTGGTGT	653361
rs782662118	snp	C/G	0.000156752	0.00885164	missense	NCF1	GRCh38.p7	7:74788677	CGCCAGGCGCGGCCG[C/G]GACCGCAGAGCCCCG	653361
rs782666062	snp	A/G	0.000146359	0.00855326	intron-variant	NCF1	GRCh38.p7	7:74779160	CCCCACCTCCCAGGT[A/G]AGCACGGGGCTGAGC	653361
rs782668137	snp	A/G	0.00014925	0.00863729	synonymous-codon	NCF1	GRCh38.p7	7:74783036	CACGGGGGACGTGGT[A/G]GAGGTCGTAGAGAAG	653361
rs782672156	in-del	-/A	1.73521e-05	0.00294546	frameshift-variant	NCF1	GRCh38.p7	7:74779374	GTCCCCACCTCCTCG[-/A]CTTCTTCAAGGTGCG	653361
rs782675140	snp	A/G	9.61418e-05	0.00693265	intron-variant	NCF1	GRCh38.p7	7:74777350	CTACGAGTTCCATGT[A/G]AGTGTGGGGACGGAG	653361
rs782680047	snp	C/G/T	0.000609383	0.0174454	intron-variant	NCF1	GRCh38.p7	7:74783509	CCTCAGTCACATTCC[C/G/T]GCACCTCTGGCACAG	653361
rs782684474	snp	A/G			intron-variant	NCF1	GRCh38.p7	7:74787566	AAATATAATCCGCCA[A/G]TGTCTTCTTTTTTCT	653361
rs782694259	snp	C/T	4.1751e-05	0.00456878	intron-variant	NCF1	GRCh38.p7	7:74783108	CCTGGTGCTCAGGAA[C/T]CCACAGCCACAAGCC	653361
rs782705862	snp	A/G	1.95792e-05	0.00312878	missense	NCF1	GRCh38.p7	7:74779343	CTCATGAGCCTGCCC[A/G]CCAAGATCTCCCGCT	653361
rs782719350	snp	C/G/T	5.30287e-05	0.00514898	synonymous-codon	NCF1	GRCh38.p7	7:74779363	GATCTCCCGCTGTCC[C/G/T]CACCTCCTCGACTTC	653361
rs782724139	snp	C/T	0.000221198	0.0105143	intron-variant	NCF1	GRCh38.p7	7:74777392	ACCCACCGTTCCAGC[C/T]CCACCCTTTGGGAAG	653361
rs782725904	snp	C/T	1.72919e-05	0.00294035	synonymous-codon	NCF1	GRCh38.p7	7:74779294	GCGGGCCGCCGAGAA[C/T]CGCCAGGGCACACTT	653361
rs782729459	snp	A/T	2.11396e-05	0.00325106	splice-donor-variant	NCF1	GRCh38.p7	7:74779424	CCCACGGACAACCAG[A/T]GAGTGAACTTTTCAC	653361
rs782730949	snp	C/T	0.000121974	0.00780845	missense	NCF1	GRCh38.p7	7:74782971	ATCCTGCAGACGTAC[C/T]GCGCCATTGCCAACT	653361
rs782732294	snp	C/T	1.67047e-05	0.00288999	synonymous-codon	NCF1	GRCh38.p7	7:74777278	CCAGGTGTACATGTT[C/T]CTGGTGAAATGGCAG	653361
rs782735248	snp	C/T	1.97046e-05	0.00313878	intron-variant	NCF1	GRCh38.p7	7:74779212	CGGGGGCTCACCTGC[C/T]CTCCCAGCCCCTCTC	653361
rs782746861	snp	A/G	0.000281017	0.0118503	intron-variant	NCF1	GRCh38.p7	7:74783265	TGTGCTTGGCAGGCC[A/G]GGGCGGGGCATGTCT	653361
rs782752617	snp	C/G	1.66255e-05	0.00288314	synonymous-codon	NCF1	GRCh38.p7	7:74783027	GGCTCTGTCCACGGG[C/G]GACGTGGTGGAGGTC	653361
rs782755612	snp	C/T	0.286243	0.247359	intron-variant	NCF1	GRCh38.p7	7:74778318	GTAGAGATGGGATTT[C/T]GCTATGTTGCCCAGG	653361
rs782759739	snp	G/T	8.44473e-05	0.00649743	missense	NCF1	GRCh38.p7	7:74783013	TCGGGCTCCGAGATG[G/T]CTCTGTCCACGGGGG	653361
rs782762643	snp	A/G	0.000101394	0.00711947	synonymous-codon	NCF1	GRCh38.p7	7:74777299	GAAATGGCAGGACCT[A/G]TCGGAGAAGGTGGTC	653361
rs782767164	snp	A/G			synonymous-codon	NCF1	GRCh38.p7	7:74783045	CGTGGTGGAGGTCGT[A/G]GAGAAGAGCGAGAGC	653361
rs782770241	snp	G/T	0.000134544	0.00820085	intron-variant	NCF1	GRCh38.p7	7:74783300	GTTCTGTCTGGATGG[G/T]TATGGGACCGTCTGT	653361
rs782772203	snp	C/T	3.5297e-05	0.00420087	intron-variant	NCF1	GRCh38.p7	7:74779227	CCTCCCAGCCCCTCT[C/T]GGGCTTGACCTCATG	653361
rs782775114	snp	A/C	0.00998311	0.0699421	intron-variant	NCF1	GRCh38.p7	7:74788734	AGAGGGCAGGAAGGG[A/C]AAGCCGTAGAGGCGG	653361
rs782778957	in-del	-/TT			intron-variant	NCF1	GRCh38.p7	7:74775948	GATTCTGGATCAGTC[-/TT]TTTTTTTTTTTTTAT	653361
rs782783154	snp	A/G	7.36974e-05	0.00606987	intron-variant	NCF1	GRCh38.p7	7:74783104	TTCCCCTGGTGCTCA[A/G]GAACCCACAGCCACA	653361
rs782786186	snp	A/G	0.000128312	0.00800872	missense	NCF1	GRCh38.p7	7:74788581	ATCCGCAACGCGCAC[A/G]GCATCCACCAGCGGT	653361
rs782787740	snp	C/G	1.68434e-05	0.00290197	missense	NCF1	GRCh38.p7	7:74782975	TGCAGACGTACCGCG[C/G]CATTGCCAACTACGA	653361
rs782794682	snp	A/G	1.70959e-05	0.00292364	synonymous-codon	NCF1	GRCh38.p7	7:74783607	CAGTCCTGACGAGAC[A/G]GAAGACCCTGAGCCC	653361
rs782794889	snp	C/T	1.66749e-05	0.00288741	missense	NCF1	GRCh38.p7	7:74783023	AGATGGCTCTGTCCA[C/T]GGGGGACGTGGTGGA	653361
rs782795751	snp	A/C	8.07461e-05	0.00635347	intron-variant	NCF1	GRCh38.p7	7:74779438	GTGAGTGAACTTTTC[A/C]CCCTGCCAGGTGGGA	653361
rs782800778	snp	C/T	0.000123199	0.00784758	missense	NCF1	GRCh38.p7	7:74777318	GAGAAGGTGGTCTAC[C/T]GGCGCTTCACCGAGA	653361
rs782811610	snp	C/T	1.7947e-05	0.00299553	intron-variant	NCF1	GRCh38.p7	7:74782929	CACCCTGCCCTCCCT[C/T]TTGCCCCAGACATCA	653361