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
rs699240	snp	C/T	0.477004	0.104734	intron-variant	NCF2	GRCh38.p7	1:183585314	CACACCATGCACAGA[C/T]CATTTTCACTGTCAG	4688
rs699241	snp	A/G	0.0919752	0.193722	intron-variant	NCF2	GRCh38.p7	1:183577367	TGCATGGTCCTTTGC[A/G]CTTCACATTAATAAA	4688
rs699242	snp	C/T	0.352287	0.228117	intron-variant	NCF2	GRCh38.p7	1:183577338	CAAAAATGAGCCCCC[C/T]GGGCTCTCTGAAGGG	4688
rs699243	snp	A/G	0.0998734	0.199905	intron-variant	NCF2	GRCh38.p7	1:183568799	AGCTATGTTCCACAG[A/G]ACACCACTGCCCCTC	4688
rs699244	snp	G/T	0.135967	0.227142	intron-variant	NCF2	GRCh38.p7	1:183556317	ACAGAATTTGTTATC[G/T]GTCACCCTTCCCCAC	4688
rs789180	snp	A/T	0.295343	0.245854	intron-variant	NCF2	GRCh38.p7	1:183556485	GTTACCAGATAGAGA[A/T]GAAGGGTCAAAGAAA	4688
rs789181	snp	A/G	0.114387	0.210022	intron-variant	NCF2	GRCh38.p7	1:183557203	AGACAACTTAGGTAT[A/G]ATCTCCAAAGCCCAC	4688
rs789182	snp	C/T	0.302435	0.244439	intron-variant	NCF2	GRCh38.p7	1:183557968	caagctccatgtccc[C/T]agttcaagtgattct	4688
rs789183	snp	C/T	0.301932	0.244547	intron-variant	NCF2	GRCh38.p7	1:183558123	aagtgatccactcac[C/T]ttggcctcccaaagt	4688
rs789184	snp	C/G	0.301932	0.244547	intron-variant	NCF2	GRCh38.p7	1:183558855	aggtgtgagccacca[C/G]gcccagccTACCCTC	4688
rs789185	snp	A/G	0.463989	0.129263	intron-variant	NCF2	GRCh38.p7	1:183585146	GCAACAGCTGCATAC[A/G]TGGGTTTTACAGGCT	4688
rs789186	snp	A/G	0.189576	0.242588	intron-variant	NCF2	GRCh38.p7	1:183585398	tgggaggccgaggcg[A/G]gtggatcacaaggtc	4688
rs789187	snp	C/G/T	0.0698336	0.173994	intron-variant	NCF2	GRCh38.p7	1:183586035	CTGTTTTGAAATCTG[C/G/T]TTTTAAATTTAACAT	4688
rs789188	snp	G/T	0.187369	0.242028	intron-variant	NCF2	GRCh38.p7	1:183586094	AATCCCAGCACTTTG[G/T]GGGGCTGAGGTGGGC	4688
rs789189	snp	C/T	0.0372196	0.131242	intron-variant	NCF2	GRCh38.p7	1:183586271	CCTGGGAGGCGGAGG[C/T]TGCGGTGAGCTGAGA	4688
rs789190	snp	C/T	0.0376037	0.131863	intron-variant	NCF2	GRCh38.p7	1:183586622	GACACTGGTGGGGTG[C/T]CACACCAGCTGAGTA	4688
rs789191	snp	A/G	0.183886	0.241099	intron-variant	NCF2	GRCh38.p7	1:183586744	GCTTCTGCCTCACCT[A/G]CTGATTTATTGCATA	4688
rs789192	snp	A/G	0.493201	0.0579089	intron-variant	NCF2	GRCh38.p7	1:183587156	CGCTCTCACATTTAG[A/G]AGCTGAAGTCTGGGA	4688
rs796860	snp	A/C	0.114036	0.209795	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555720	TGTTTTTGTAAGATG[A/C]TAGGTTTTTTTTTAT	4688
rs1126596	snp	C/T			synonymous-codon	NCF2	GRCh38.p7	1:183566949	CTTGAACCAGTTGAG[C/T]TGCGGATCCACCCTC	4688
rs2236384	snp	C/G	0.499502	0.0157669	intron-variant	NCF2	GRCh38.p7	1:183568724	TGCCCCCGTCAGAGG[C/G]GACTGCAGCCAGTGC	4688
rs2236385	snp	A/G	0.495818	0.0455352	intron-variant	NCF2	GRCh38.p7	1:183568890	ACGTAGCTGCAGCCA[A/G]GCCCTGATGGCCAGC	4688
rs2274064	snp	C/T	0.499779	0.0105108	missense, intron-variant	NCF2	GRCh38.p7	1:183573252	TTTGGTCGAAACAGC[C/T]TGCCCACAGGGATCA	4688
rs2274065	snp	A/C	0.325091	0.238456	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590569	gagagaaaaggaaag[A/C]agcagagagagagag	4688
rs2296164	snp	C/T	0.499437	0.0167719	intron-variant	NCF2	GRCh38.p7	1:183565800	GGCAACAGGGAGCGA[C/T]GGTCAGAACCTTCAT	4688
rs2296165	snp	C/T	0.0182019	0.0936463	intron-variant	NCF2	GRCh38.p7	1:183586828	CTCAAACACCAAGCC[C/T]GCAACACTGAGACCC	4688
rs2308167	in-del	-/TGTT	0.462187	0.132199	downstream-variant-500B	NCF2	GRCh38.p7	1:183555507	CTCTGTGGAATTGAG[-/TGTT]TGTTGTAGTCCATGA	4688
rs2333681	snp	C/T	0.327211	0.237778	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590726	AGCTTCTGGCCAAAG[C/T]TCTGCTTCTAGAGCC	4688
rs2333682	snp	A/G	0.32768	0.237625	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591626	TAGCTGGGATTACAG[A/G]AGCCTGCCACCACGC	4688
rs2333683	snp	A/G	0.177503	0.239258	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591722	aactcctgacctcag[A/G]tgattcggcctcctc	4688
rs3768582	snp	A/G	0.351418	0.228505	intron-variant	NCF2	GRCh38.p7	1:183584735	ACTCCCCCTTACCCC[A/G]TCTCCAGACTATAGA	4688
rs3768583	snp	A/T	0.49949	0.0159663	intron-variant	NCF2	GRCh38.p7	1:183569590	AAAAAAATTTTTTTT[A/T]AATTAATTTAAAAAT	4688
rs3768584	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183567905	TCAGACTTAAGGGAA[C/T]CGACACTGCACCACG	4688
rs3818364	snp	G/T	0.49975	0.0111793	intron-variant	NCF2	GRCh38.p7	1:183573612	CACCACCACGACAAG[G/T]CTGGCCCGGGATCAA	4688
rs3820690	snp	A/G	0.299158	0.245119	intron-variant	NCF2	GRCh38.p7	1:183582027	GGCCTGCAGCAGGGA[A/G]CGAGGGGGCTGGGAA	4688
rs3820691	snp	C/T	0.499741	0.0113788	intron-variant	NCF2	GRCh38.p7	1:183569990	AGGCCATGAGGGGAA[C/T]GCAGCCCAGGTAACT	4688
rs3843292	snp	A/G	0.0314385	0.121371	intron-variant	NCF2	GRCh38.p7	1:183561366	AGAGTCCACAGAGAA[A/G]ggtttgtatcccacc	4688
rs3843293	snp	G/T	0.49934	0.0181589	intron-variant	NCF2	GRCh38.p7	1:183570314	GTTCACTCTCAGTGC[G/T]CTGCCTGTGTTCCCG	4688
rs3845461	snp	A/G	0.126909	0.217598	intron-variant	NCF2	GRCh38.p7	1:183563065	GGGAGGCAGAGCTGT[A/G]ACTTATTACACACCA	4688
rs3845462	snp	G/T	0.49621	0.0433651	intron-variant	NCF2	GRCh38.p7	1:183568339	ACTCAGCTAATTTTT[G/T]CATGTTTAGTAGACA	4688
rs3845463	snp	G/T	0.499477	0.0161657	intron-variant	NCF2	GRCh38.p7	1:183568343	AGCTAATTTTTTCAT[G/T]TTTAGTAGACATGGG	4688
rs3845464	snp	A/C	0.499801	0.00998203	intron-variant	NCF2	GRCh38.p7	1:183572707	TACAGTGGTGCAATC[A/C]TAGCTCACTGTAGCC	4688
rs3845465	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183572731	TGTAGCCTTGAACTC[C/T]TGGGCTCAAGTGATC	4688
rs3845466	snp	A/G	0.325327	0.238382	intron-variant	NCF2	GRCh38.p7	1:183582625	AAGTCAAAACTTCAG[A/G]CATCTTTGGGATGCT	4688
rs3903837	snp	C/T	0.416545	0.186448	intron-variant	NCF2	GRCh38.p7	1:183587485	TGTGGTCCCAGCTAC[C/T]TGGGGGACTGAGGTA	4688
rs3905122	snp	C/T	0.067446	0.170804	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592900	TGCATCTGTGBGACT[C/T]GTGCTAGTTCCTCTT	4688
rs3929721	snp	C/T	0.175897	0.238765	intron-variant	NCF2	GRCh38.p7	1:183579508	gaggcgggtggatca[C/T]gaggtcaggagatcg	4688
rs4652813	snp	C/G	0.178465	0.239547	intron-variant	NCF2	GRCh38.p7	1:183565409	TTCTTCCTGAGACAT[C/G]GTTTCCCTACCTAAT	4688
rs4987079	snp	A/G	0.191775	0.243125	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591061	aggaaagtcccccca[A/G]tgcgggtgagtctgg	4688
rs4987080	snp	A/G	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591057	aagtccccccagtgc[A/G]ggtgagtctggggct	4688
rs6667363	snp	C/T	0.499793	0.0101816	intron-variant	NCF2	GRCh38.p7	1:183571963	cgtagtattctgttg[C/T]atggatatatcacat	4688
rs6668645	snp	A/G	0.0341408	0.126114	intron-variant	NCF2	GRCh38.p7	1:183567126	TCTGCAAAGAAGGCA[A/G]CAGATACTGCTCCAC	4688
rs7520027	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557025	TTTGTTAAATATAAA[C/T]ATTTTAATAGCTCCT	4688
rs7521394	snp	A/C	0.0391387	0.134304	intron-variant	NCF2	GRCh38.p7	1:183584502	GGTCTTACTTTTAGA[A/C]GTTTCCAAGATCTTT	4688
rs7531724	snp	A/G/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183580775	tgaggtcaggggttc[A/G/T]agaccagcctggcca	4688
rs9425306	snp	A/G	0.304937	0.243889	intron-variant	NCF2	GRCh38.p7	1:183560519	AGATGAATGGTGGTG[A/G]GTGGTGGGTTGGGGG	4688
rs10689990	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183578356	CCTCCTTTTTTTTTT[-/T]CTTTTTTTTTGAGAC	4688
rs10797887	snp	A/G	0.231482	0.249313	intron-variant	NCF2	GRCh38.p7	1:183575559	CAGAATCAAATAATC[A/G]TTTGGATGCATTACC	4688
rs10797888	snp	C/T	0.14933	0.228835	intron-variant	NCF2	GRCh38.p7	1:183577897	CCTTGGGAATGGTGT[C/T]CCCCCCAGGGCTGTG	4688
rs10911357	snp	G/T	0.499325	0.0183582	intron-variant	NCF2	GRCh38.p7	1:183571641	TTTTAAAAATCAGAT[G/T]TAAAGCTAGCTTTAT	4688
rs10911358	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183571991	cattttgattactca[C/T]tcatcagttgataga	4688
rs10911359	snp	C/T	0.499784	0.0103811	intron-variant	NCF2	GRCh38.p7	1:183573918	AACATGGCAAAACCC[C/T]GTCTCTATTAAAAAT	4688
rs10911360	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576990	TCTCCCTTTTGATAA[C/T]AGAGAAAAGAAGTTG	4688
rs10911361	snp	C/T	0.29046	0.246704	intron-variant	NCF2	GRCh38.p7	1:183579361	TTTGAGTCTTGGCTC[C/T]GTCACTTACTATCTG	4688
rs10911362	snp	A/G	0.295854	0.245759	intron-variant	NCF2	GRCh38.p7	1:183579857	TGCCTGGCACACACC[A/G]TAATTTTTTTACTAT	4688
rs10911363	snp	G/T	0.46845	0.121572	intron-variant	NCF2	GRCh38.p7	1:183580622	GAAGTGACACCACCT[G/T]GGTCTATCTGGCATT	4688
rs10911364	snp	A/G	0.169435	0.236663	intron-variant	NCF2	GRCh38.p7	1:183583391	ACACATTAAGAAGTA[A/G]TTTCTCTAGCCCCCA	4688
rs10911365	snp	A/G	0.323434	0.238972	intron-variant	NCF2	GRCh38.p7	1:183589970	TGCTCTCCACCTGGA[A/G]AGCTTTTAAAACTGG	4688
rs10911366	snp	C/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592150	TAGCAACTGAAAGAA[C/T]TCACTCATTATCACC	4688
rs10911367	snp	C/T	0.484632	0.086302	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592382	TGCTAAATCTAGCCC[C/T]GAACTCTGGGTAGTA	4688
rs11287969	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183587625	AAAAAAAAAAAAAAA[-/A]TCCAATGATACAAAT	4688
rs11414367	in-del	-/A	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183580979	CAAAAAAAAAAAAAA[-/A]GGTGTCTACAGATTT	4688
rs11540867	snp	C/T			utr-variant-5-prime	NCF2	GRCh38.p7	1:183590341	TCTTGGCCTCCTAGT[C/T]TCTACCTAATCATGT	4688
rs11577618	snp	C/T	0.0622301	0.165053	intron-variant	NCF2	GRCh38.p7	1:183568691	ATTCTAGATTCCTGA[C/T]TCCAGAGAGCTCTGG	4688
rs11578964	snp	C/T	0.416218	0.186739	intron-variant	NCF2	GRCh38.p7	1:183586644	AGCTGAGTATCAGGC[C/T]CATGGTGGTTACCTA	4688
rs11588654	snp	C/T	0.301429	0.244653	intron-variant	NCF2	GRCh38.p7	1:183587260	ATACCATCTGATTTC[C/T]GCTTTTGTTAGTCAT	4688
rs11590384	snp	A/C	0	0	intron-variant	NCF2	GRCh38.p7	1:183587296	GCCTAGAAAAGCTAC[A/C]CAAGAATCCAATAAT	4688
rs11806305	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183561842	tctctctgtcaccca[A/G]actggagtgcagtgg	4688
rs11811630	snp	C/T	0.499203	0.0199521	intron-variant	NCF2	GRCh38.p7	1:183564775	ATTGAGCAGGAGCAA[C/T]GGGAGAAATTTGAAT	4688
rs12022723	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183561905	tgggttcaagcaatt[C/T]tgcctcagcctccca	4688
rs12027051	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587292	TATGGCCTAGAAAAG[C/T]TACACAAGAATCCAA	4688
rs12027057	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587327	TCccaggtgcggttg[C/T]tcacacctgtaatcc	4688
rs12027823	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587481	tgcctgtggtcccag[C/T]tacttgggggactga	4688
rs12036973	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183561913	agcaattctgcctca[A/G]cctcccaagtagctg	4688
rs12045169	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183580833	aatatttaaaaatta[C/G]ccgggcgtggtggtg	4688
rs12046252	snp	A/G	0.302184	0.244493	intron-variant	NCF2	GRCh38.p7	1:183581910	CTTACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	4688
rs12057355	snp	G/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592306	AGGCCTTCCCAGCTC[G/T]CTTCTTTGCCTGGCA	4688
rs12066019	snp	A/C	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592425	TCTCCTTTGTACCAC[A/C]TTTACCCAAAAACTT	4688
rs12066221	snp	A/C	0.0182019	0.0936463	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592769	TATCCCACCCTGACA[A/C]TCAGAACTCTCCTTA	4688
rs12086606	snp	C/G	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592383	GCTAAATCTAGCCCT[C/G]AACTCTGGGTAGTAG	4688
rs12086699	snp	G/T	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592590	AATTAGAAATCATTG[G/T]TAAATGACCTGCAGG	4688
rs12091406	snp	A/G	0.192401	0.243274	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590706	TCCCACCCCTGTTCT[A/G]TGGCAGCTTCTGGCC	4688
rs12091848	snp	C/T	0.327914	0.237549	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592389	TCTAGCCCTGAACTC[C/T]GGGTAGTAGGAGAAT	4688
rs12094036	snp	C/T	0.324145	0.238752	intron-variant	NCF2	GRCh38.p7	1:183589039	GTGGGGCCATGTCCT[C/T]CCTCCAGCCAGAGGT	4688
rs12094228	snp	G/T	0.287346	0.247195	intron-variant	NCF2	GRCh38.p7	1:183578737	AGCTGACTGGCTCGA[G/T]GTATACCAGGGCTGC	4688
rs12095261	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183571081	AAAAGAAATGttttt[A/T]attgaggtgcaattt	4688
rs12095618	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183579568	catctctactaaaaa[A/T]aaaaaaataaaaaaa	4688
rs12096702	snp	A/G	0.192088	0.2432	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592562	ACATGATGAAGGGAT[A/G]CATTCTAAAAGAAAT	4688
rs12119260	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183581315	aagaaagaaaGAAAG[A/G]AAAGAAAGTCCAACA	4688
rs12122217	snp	C/T	0.482309	0.0923707	intron-variant	NCF2	GRCh38.p7	1:183576530	CCACGATGCGCAGGA[C/T]GCACCACAACCCCTC	4688
rs12141638	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183581314	aaagaaagaaaGAAA[A/G]AAAAGAAAGTCCAAC	4688
rs12405210	snp	A/G	0.276534	0.248588	intron-variant	NCF2	GRCh38.p7	1:183562803	acacccagcttgggc[A/G]acagagtgagactcc	4688
rs12568414	snp	A/C	0	0	intron-variant	NCF2	GRCh38.p7	1:183574636	CCTAGAAAAGTACAG[A/C]CCGCAACATAAAACT	4688
rs12737538	snp	A/G	0.397452	0.201886	intron-variant	NCF2	GRCh38.p7	1:183581298	aaaaaaaaaaaaaaa[A/G]aaagaaagaaaGAAA	4688
rs12740417	snp	C/T	0.355954	0.226437	intron-variant	NCF2	GRCh38.p7	1:183584425	ATTACAGATAAAACT[C/T]GGTAGATTTTTCTCT	4688
rs12753665	snp	A/G	0.479984	0.0980171	intron-variant	NCF2	GRCh38.p7	1:183576926	GGAGGGGTGGGAAGG[A/G]CCAACCGGAAAAAGT	4688
rs13306575	snp	C/T	0.0297936	0.118363	NCF2	1	allele_origin=T(germline)/C(germline)	1:183563302	TCCCCACSCAGCTAT[C/T]GGCCTCGGGACAGCA	4688
rs13306576	snp	A/G	0.00835141	0.0640778	intron-variant	NCF2	GRCh38.p7	1:183577862	GTATAGAATACTTGG[A/G]CTCAGGGTTGCTGAA	4688
rs13306577	in-del	-/ATC	0.28875	0.246979	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555715	AAAAAACCTATCATC[-/ATC]TTACAAAAACAAGAC	4688
rs13306580	snp	C/T	0.193028	0.243422	upstream-variant-2KB, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590900	TCTCACTCTAGGTCA[C/T]GGGTTTCATTTGGGA	4688
rs13306581	snp	C/T	0.00457908	0.0476301	missense	NCF2	GRCh38.p7	1:183567223	ATGATAACTGGGCCA[C/T]GGTCATGTTCAACGG	4688
rs13306582	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565547	GAATCCCCCTTTCCT[A/G]CACCACCCACCCCAA	4688
rs13306583	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183565530	ACCACCCACCCCAAA[C/T]ATGAAATCAGTGCCC	4688
rs13374239	snp	C/T	0.0271762	0.113356	intron-variant	NCF2	GRCh38.p7	1:183576103	AGAAAAACCTTGACA[C/T]TCTTCAAAAATAATG	4688
rs16861162	snp	C/T	0.0134861	0.0810011	intron-variant	NCF2	GRCh38.p7	1:183562528	AGCTTTATACACTGC[C/T]CTTTTCTAGGCTCAT	4688
rs16861163	snp	C/T	0.00326414	0.0402668	intron-variant	NCF2	GRCh38.p7	1:183564082	TGGTGAATGAACATC[C/T]TTGGCCAGCCCCTGC	4688
rs16861188	snp	A/G	0.0138799	0.0821421	intron-variant	NCF2	GRCh38.p7	1:183584191	TCACATACGGACTTC[A/G]TATCTATAGCCCCTG	4688
rs17849501	snp	C/T	0.0658721	0.169106	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573188	AATCCCACCTACCGT[C/T]GCCTTGCCTAGGTAA	4688
rs17849502	snp	G/T	0.066217	0.169483	missense	NCF2	GRCh38.p7	1:183563445	TCACCTCAGCTTAGT[G/T]TGTTCCAGCCGGAGC	4688
rs28385883	snp	G/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592223	ACTCCACAGTGCTTG[G/T]AGGATTGAAGGTGTG	4688
rs28602604	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183559295	AGCCTCCCTAGTGGC[G/T]AGGATTACAGGCATG	4688
rs34009795	snp	C/G	0.00356857	0.0420898	intron-variant	NCF2	GRCh38.p7	1:183590148	CAGAGAAGGTGAGTG[C/G]AGGTGCCTCTTTCCG	4688
rs34014596	snp	A/G	0.0170251	0.090679	intron-variant	NCF2	GRCh38.p7	1:183585642	GGCTCAGGCTAATGA[A/G]GAATTTTTTTTTTTT	4688
rs34015031	snp	A/G	0.0236746	0.106192	intron-variant	NCF2	GRCh38.p7	1:183565007	AATAAACATCAGAAT[A/G]TCTTTCACTTAAACT	4688
rs34018429	snp	C/G	0.00676609	0.0577691	intron-variant	NCF2	GRCh38.p7	1:183562481	CCGTTCAGAAAATTG[C/G]CTTCAGGAAATACAG	4688
rs34033715	snp	G/T	0.0134861	0.0810011	intron-variant	NCF2	GRCh38.p7	1:183570916	AAGAACAGGTCTAGG[G/T]CATGAGCAAAGAGGG	4688
rs34035622	in-del	-/TTC	0.0170251	0.090679	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555843	CACGAGAGAGTCTTC[-/TTC]CAGGTACTGATCCTG	4688
rs34110768	snp	C/T	0.171057	0.237209	intron-variant	NCF2	GRCh38.p7	1:183589861	GAAGGCTGTCCTAGT[C/T]GTACTTTCTTCTACA	4688
rs34157425	snp	G/T	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183581911	GGGAGGCCGAGGCGG[G/T]CGGATCACGAGGTAA	4688
rs34157444	snp	C/T	0.00755907	0.0610114	intron-variant	NCF2	GRCh38.p7	1:183581869	CCATCCTGGCTAACA[C/T]GGTGAAACCCTGGCT	4688
rs34158094	snp	A/G	0.000989805	0.0222244	intron-variant	NCF2	GRCh38.p7	1:183573343	GGAGGCAGGACAAGC[A/G]TCGTCACCCCCATTT	4688
rs34192123	snp	G/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183559308	AAAATTGAAACAGCA[G/T]GCCTGTAATCCTAGC	4688
rs34194274	snp	A/C	0.177503	0.239258	intron-variant	NCF2	GRCh38.p7	1:183589668	AGTGACAATTCTGAT[A/C]AATTATAAAGGAGAC	4688
rs34212890	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583684	CCTTTTGTAATATGT[A/C]TGGCCCGTGACAGAT	4688
rs34229284	snp	A/G	0.0325976	0.123435	intron-variant	NCF2	GRCh38.p7	1:183583989	CACTGCCTTGGTTGA[A/G]ACCCTCATTTTTCAC	4688
rs34307026	snp	C/T	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183576505	TCGTGGGAACTTTGA[C/T]GGCATCTCTAGCTTT	4688
rs34356361	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183579193	GCTCTGCCACTAACT[-/G]GGGGGACCCTAGCAA	4688
rs34423782	snp	A/G	0.179744	0.239925	intron-variant	NCF2	GRCh38.p7	1:183585579	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	4688
rs34446955	snp	A/G	0.0182019	0.0936463	intron-variant	NCF2	GRCh38.p7	1:183568948	AGAATGTCAGGCTAG[A/G]AAGGAATGATATGAT	4688
rs34453439	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183567891	ACCGACACTGCACCA[C/T]GGCAGCTGGGCAGCC	4688
rs34459587	snp	C/T	0.324145	0.238752	intron-variant	NCF2	GRCh38.p7	1:183589222	AAGGTGTGGCAGTGG[C/T]TGACTCCCCAGGTCC	4688
rs34496837	snp	A/G	0.0263992	0.111815	intron-variant	NCF2	GRCh38.p7	1:183587126	GAAGTGGGGTGCACC[A/G]TGAGAGCACAGGGTG	4688
rs34501573	snp	C/T	0.00710448	0.0591757	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590458	GGAGGCTGGGCCCCA[C/T]TCTACTCATCTGGCC	4688
rs34513796	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183585571	AGAGGTTGCAGTGAG[-/C]CCGAGATCGCGCCAC	4688
rs34560544	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183561172	CATCCTTCTCCTTCA[C/T]TTGTGAAGCAAAAGT	4688
rs34580772	snp	G/T	0.0193772	0.0965046	intron-variant	NCF2	GRCh38.p7	1:183561141	GACAATAATGTGGAA[G/T]AAGTCTAAGATCATA	4688
rs34680162	snp	G/T	0.0178098	0.0926698	intron-variant	NCF2	GRCh38.p7	1:183569299	TCAGTCAGAAATGCG[G/T]TATTTGATTTTCTGG	4688
rs34708305	in-del	-/G	0.0452528	0.143452	intron-variant	NCF2	GRCh38.p7	1:183566668	TGTGACTCTTCCTGG[-/G]TCAGAAGTCACTTGG	4688
rs34711286	snp	A/G	0.0283406	0.115616	intron-variant	NCF2	GRCh38.p7	1:183584433	TACACCTGAGAGAAA[A/G]ATCTACCAAGTTTTA	4688
rs34712183	in-del	-/T	0.314301	0.241589	intron-variant	NCF2	GRCh38.p7	1:183582958	TTTCCCCACTTTCGT[-/T]ATGTTTTTGTGTTGC	4688
rs34715440	snp	C/G	0.416545	0.186448	intron-variant	NCF2	GRCh38.p7	1:183586238	CAAGCGATTCTCCTG[C/G]CTTACCCTCCCGAGT	4688
rs34764302	in-del	-/T	0.0162398	0.0886349	intron-variant	NCF2	GRCh38.p7	1:183588612	ATATAATATTTTAAT[-/T]ATTTTCATTTGCAAT	4688
rs34823167	snp	G/T	0.0275645	0.114116	intron-variant	NCF2	GRCh38.p7	1:183565546	TTTGGGGTGGGTGGT[G/T]CAGGAAAGGGGGATT	4688
rs34844414	snp	A/G	0.0210502	0.100409	intron-variant	NCF2	GRCh38.p7	1:183575856	CCCCCACCATTCAGC[A/G]CCAGCCACTAATGCC	4688
rs34862135	snp	C/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183583909	TCCCCTCCATTCATA[C/T]TCCAGAGTGATCTTG	4688
rs34907425	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582523	CTGGCAGCATGGGAA[C/T]AAGCAGGTTACTAAG	4688
rs34956009	snp	C/T	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183569301	CATCAGTCAGAAATG[C/T]GTTATTTGATTTTCT	4688
rs34990556	snp	A/C	0.00398564	0.0444627	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592054	TGGATTTTAGCAAGC[A/C]AAATTGGCTATACCC	4688
rs35009190	snp	A/G	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183571376	TAATCCCAGCACTTT[A/G]GGAGGCTGGATGGGT	4688
rs35012521	snp	A/T	0.0106837	0.0723028	missense	NCF2	GRCh38.p7	1:183563229	GGGGCCAGGTGAAAA[A/T]CTACTGCCTGACTCT	4688
rs35028236	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183571207	ACTGCAACCTCTGCC[-/T]TCCAGGTTCAAGTGA	4688
rs35036437	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183558697	GCCTCCCTAGCAGCT[-/G]GGGACTACAGATGTG	4688
rs35047617	snp	C/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183587075	GGCAGACAGCAGAGC[C/T]GGGCACCACAGGGAG	4688
rs35048410	snp	C/G	0.0162398	0.0886349	intron-variant	NCF2	GRCh38.p7	1:183581747	CGGGAGGCGGAGCTT[C/G]CAGTGAGCCGAGATC	4688
rs35049461	snp	C/T	0.416545	0.186448	intron-variant	NCF2	GRCh38.p7	1:183586235	GCGATTCTCCTGGCT[C/T]ACCCTCCCGAGTAGC	4688
rs35054092	snp	C/G	0.0244538	0.107838	intron-variant	NCF2	GRCh38.p7	1:183567790	CAACACTGGTTCTAG[C/G]TGGTTTCTCCTTCCT	4688
rs35059212	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579159	GGATCTGGACTCTGG[C/T]TCCTGGCCCCTTTAC	4688
rs35066000	in-del	-/A	0.116488	0.211364	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590577	TACTCGCCCTCTCTC[-/A]TCTCTGCTTCTTTCC	4688
rs35081682	snp	C/T	0.0197687	0.0974348	intron-variant	NCF2	GRCh38.p7	1:183568467	GGTTTTAAAAAGTGA[C/T]TGGCCAGGTGTGTGG	4688
rs35085013	snp	A/C	0.0271762	0.113356	intron-variant	NCF2	GRCh38.p7	1:183581957	TTAGTTGGCGAGGCG[A/C]GGTGGCTCACGCCTG	4688
rs35109762	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183565358	AACAGCCACTCCATG[-/C]CCCTCAGAGATAAGC	4688
rs35116326	in-del	-/T			utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590418	GCAGGGCTGCCTTAG[-/T]GGCCCCCAAGGTGTT	4688
rs35123412	in-del	-/CTTAC/TTAC	0.0329836	0.124112	downstream-variant-500B	NCF2	GRCh38.p7	1:183555253	CTAGAGTGCACTTAC[-/CTTAC/TTAC]ACAAGACTAGATGGT	4688
rs35131781	snp	C/T	0.0298908	0.118541	intron-variant	NCF2	GRCh38.p7	1:183586504	TTCATCCCAGCAAAA[C/T]GCATTTCCAAAACCT	4688
rs35146388	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566876	TCCAGGGAGAGATCC[C/T]TAAAGGGTGAGAGGA	4688
rs35153426	snp	A/G	0.0119091	0.0762411	intron-variant	NCF2	GRCh38.p7	1:183575252	AAACTCCTGACCTCA[A/G]GTGATTCACCCGCCT	4688
rs35184007	in-del	-/T	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183588628	ACAAATATAACAATT[-/T]ATATAATATTTTAAT	4688
rs35193454	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183578521	GGCGAGCGCCACCAC[-/G]GCCCGGCTAATTTTT	4688
rs35205865	snp	A/T	0.0210502	0.100409	intron-variant	NCF2	GRCh38.p7	1:183579991	TATGCCATGTATTTT[A/T]AAAATATCCTGATAA	4688
rs35214000	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569598	CCATCTCAAAAAAAA[A/T]TTTTTTTAAATTAAT	4688
rs35222366	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183559603	CTAAAGTACTGAGAT[C/T]ACAGGCATGAGCCAC	4688
rs35231707	snp	C/T	0.0345262	0.126772	intron-variant	NCF2	GRCh38.p7	1:183585612	TTTGAGACGGAGTTT[C/T]GCCCTGTCACCCAGG	4688
rs35238239	snp	A/G	0.0383715	0.133092	intron-variant	NCF2	GRCh38.p7	1:183584533	GATCTGGAAGGCCAC[A/G]GTTTTGAGTGATTAG	4688
rs35304105	snp	G/T	0.301429	0.244653	intron-variant	NCF2	GRCh38.p7	1:183586319	GAGACAGAGTTTCAC[G/T]CTTGTTGCCCAGGCT	4688
rs35327744	snp	C/T	0.0210502	0.100409	intron-variant	NCF2	GRCh38.p7	1:183563920	TGTCTGTCTGGATTA[C/T]AGGAAGAGCCCCAAA	4688
rs35330145	snp	C/T	0.0210502	0.100409	intron-variant	NCF2	GRCh38.p7	1:183562439	GAGACTCCCTGGTGT[C/T]TCTGGCTGAGACAAA	4688
rs35331687	snp	C/T	0.0279526	0.114869	intron-variant	NCF2	GRCh38.p7	1:183588458	AGATGGAGTCTCACT[C/T]TGTCACCCAGGCTGG	4688
rs35394013	snp	C/T	0.177503	0.239258	intron-variant	NCF2	GRCh38.p7	1:183589806	CTCTATCTATCCCAG[C/T]GCTTTACACCTGATT	4688
rs35423398	snp	C/T	0.324382	0.238678	intron-variant	NCF2	GRCh38.p7	1:183589303	CAAACTATTAATGTC[C/T]CGTGGAACTTCACAC	4688
rs35433887	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183565896	ACATGCAGATAACGT[-/C]CTAAAAGTTGGAATG	4688
rs35439705	snp	C/G	0.0271762	0.113356	intron-variant	NCF2	GRCh38.p7	1:183587661	ATTAGTGTCTGCACC[C/G]TTATAGTCCACTTTG	4688
rs35445836	snp	A/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183583875	AATAAAAAAAAATTT[A/T]AAAAAAGCAATCTCT	4688
rs35455410	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183577952	TCTTGGACAGTCACA[-/G]GGGAGTTTCTTCTCT	4688
rs35471511	in-del	-/C	0.0107246	0.0724382	intron-variant	NCF2	GRCh38.p7	1:183575441	TTACCATTCCCCCCC[-/C]ACCTGAGGTGAAGGT	4688
rs35504102	snp	A/G	0.00875997	0.0655991	intron-variant	NCF2	GRCh38.p7	1:183565810	GGAACTTTGAATGAA[A/G]GTTCTGACCRTCGCT	4688
rs35514775	snp	C/T	0.0463947	0.145069	intron-variant	NCF2	GRCh38.p7	1:183573732	TGAATAAGGCTAGCT[C/T]TAAATCTGATTTTTA	4688
rs35550074	snp	C/T	0.485596	0.0836329	intron-variant	NCF2	GRCh38.p7	1:183589302	AAACTATTAATGTCT[C/T]GTGGAACTTCACACC	4688
rs35552352	in-del	-/G			upstream-variant-2KB, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590863	CAAAAACAGCCTGAA[-/G]GCTGAAAGACTAGGC	4688
rs35556454	snp	A/G	0.0217236	0.101931	intron-variant	NCF2	GRCh38.p7	1:183575123	CTGGTGCTGGTACAG[A/G]AGGTTGCATCTTGAT	4688
rs35571284	in-del	-/T	0.0103295	0.0711199	intron-variant	NCF2	GRCh38.p7	1:183585043	AGAAGTGAAGTCTTT[-/T]CTAAAAGAAAAACCA	4688
rs35587632	snp	A/T	0.00676609	0.0577691	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592049	TTTAGCAAGCCAAAT[A/T]GGCTATACCCTTTAC	4688
rs35613470	snp	C/T	0.0174175	0.0916809	intron-variant	NCF2	GRCh38.p7	1:183585410	TCTCGAACTCCTGAC[C/T]TTGTGATCCACCCGC	4688
rs35648088	in-del	-/TGGCTTTCCAAGACTTTCAT	0.115438	0.210697	intron-variant	NCF2	GRCh38.p7	1:183589749	CTAAGGCACCTCTTT[-/TGGCTTTCCAAGACTTTCAT]GTGTGTCGACTTTGC	4688
rs35667872	snp	C/T	0.324382	0.238678	intron-variant	NCF2	GRCh38.p7	1:183589288	TCGTGGAACTTCACA[C/T]CACTGTATAAGAGTT	4688
rs35681596	snp	A/T	0.000397562	0.0140934	utr-variant-5-prime	NCF2	GRCh38.p7	1:183590333	TCCTAGTTTCTACCT[A/T]ATCATGTCCCTGGTG	4688
rs35714051	snp	C/T	0.0138799	0.0821421	intron-variant	NCF2	GRCh38.p7	1:183571279	AATACAAAAATTAGC[C/T]GGGCACAGTGGCGGG	4688
rs35734725	snp	A/C	0.465368	0.126951	intron-variant	NCF2	GRCh38.p7	1:183581340	CCAACAACCAAAAAA[A/C]CAGGGTGGGGCCAGG	4688
rs35813663	snp	A/G	0.046775	0.145601	intron-variant	NCF2	GRCh38.p7	1:183575593	AAATTTATTTCAGTC[A/G]GGCCATTTTTTAGAT	4688
rs35824065	snp	A/G	0.0217236	0.101931	intron-variant	NCF2	GRCh38.p7	1:183587821	ATGTCTAAATTATCT[A/G]TTCTGAATTCTAGTC	4688
rs35825609	snp	C/T	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183578141	GCCAGGCTGGCCTGG[C/T]CTGATGGTGGGAGCC	4688
rs35832000	snp	A/G	0.177503	0.239258	intron-variant	NCF2	GRCh38.p7	1:183589143	CAGCCACACCCTCCT[A/G]ACAGGAAGACAGAGA	4688
rs35836322	in-del	-/T	0.0970103	0.197722	intron-variant	NCF2	GRCh38.p7	1:183584917	TATTTATTGTGACTT[-/T]ATAAATTCTTTTTTT	4688
rs35847656	snp	A/T	0.0197687	0.0974348	intron-variant	NCF2	GRCh38.p7	1:183588206	GTGTTGGATAGGAAT[A/T]GTATCTTTAAGTTTG	4688
rs35916153	snp	A/G	0.00557542	0.0525036	intron-variant	NCF2	GRCh38.p7	1:183581754	CGTGAACCGGGAGGC[A/G]GAGCTTCCAGTGAGC	4688
rs35936159	snp	G/T	0.0970103	0.197722	intron-variant	NCF2	GRCh38.p7	1:183584915	TTTATTGTGACTTTA[G/T]AAATTCTTTTTTTAA	4688
rs35937854	snp	C/T	0.00742068	0.0604589	missense	NCF2	GRCh38.p7	1:183566954	ACTACCTTGAACCAG[C/T]TGAGCTGCGGATCCA	4688
rs35953580	snp	A/C	0.0189856	0.0955633	intron-variant	NCF2	GRCh38.p7	1:183577385	TTACCTGGGGGCATA[A/C]ATTTTATTAATGTGA	4688
rs35971401	snp	C/T	6.58892e-05	0.00573936	intron-variant	NCF2	GRCh38.p7	1:183569104	AATAGAATATCCAAG[C/T]GCCAAGCCTGAGCTG	4688
rs35997828	snp	A/G	0.02016	0.0983543	intron-variant	NCF2	GRCh38.p7	1:183587186	GAATGACAATACAAG[A/G]AATGCACACCATTGT	4688
rs36013653	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183585548	AACCTCTGCCTTCCA[C/T]GTTCAAACAATTCTC	4688
rs36029527	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585396	CCTTGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	4688
rs36049229	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183586523	AACTGCATCAAAACC[C/T]GGCTTCATCCCAGCA	4688
rs36051480	snp	A/G	0.0279526	0.114869	intron-variant	NCF2	GRCh38.p7	1:183586379	GTAGCGTATGCACTT[A/G]TACAGAAAAAGTTTG	4688
rs36071574	snp	C/T	0.122411	0.214991	intron-variant	NCF2	GRCh38.p7	1:183576468	CTACTAGCACTGCCA[C/T]CACCACTCCCCACCC	4688
rs36083816	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183570374	TGGGCCTGAGGTTTG[A/G]GCTCTCCTGGCTCTA	4688
rs36101819	snp	A/G	0.0588605	0.161139	intron-variant	NCF2	GRCh38.p7	1:183575542	ATTATTTGATTCTGT[A/G]TGTAAATTGTGAAGC	4688
rs36112043	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183557628	ACAATATGGGTATTT[-/T]CCTCAACTTAGACTT	4688
rs36113295	snp	G/T	0.0255946	0.110192	intron-variant	NCF2	GRCh38.p7	1:183564040	TTTACTCCCTACTTT[G/T]TCCATTCAGGCCAGA	4688
rs55651413	snp	C/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183577506	GCTTTTCCAAGCTCC[C/T]GGAGGTGTCAACAGA	4688
rs55652036	in-del	-/ATGAAA	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183565973	GGTGGAGTTGGCCTG[-/ATGAAA]ATGAAAATCACAGTA	4688
rs55677357	snp	A/C	0.00795532	0.062565	upstream-variant-2KB	NCF2	GRCh38.p7	1:183590977	CTAATGCCTTTTAAC[A/C]AATTGAATGTTGCCT	4688
rs55685212	snp	A/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183559977	TAGATGCTAGGAAGG[A/G]GGTTGAAAACACTGG	4688
rs55761650	snp	A/G	0.00820277	0.0635146	missense	NCF2	GRCh38.p7	1:183560204	CTTTCTTAAGCTGAG[A/G]TTCTGTTGTCTGGTT	4688
rs55790185	snp	A/C/G/T	0.00547164	0.052028	intron-variant	NCF2	GRCh38.p7	1:183573143	TGCTCCACATGGCCC[A/C/G/T]GGCCACAGGAGACTC	4688
rs55795842	snp	C/G	0.0031251	0.0394053	intron-variant	NCF2	GRCh38.p7	1:183563310	CGAGGCCRATAGCTG[C/G]GTGGGGATAATGAGT	4688
rs55832218	snp	C/T	0.00131744	0.0256317	intron-variant	NCF2	GRCh38.p7	1:183574637	CTAGAAAAGTACAGA[C/T]CGCAACATAAAACTT	4688
rs55854442	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183590966	ATTATTTCTGACTAA[C/T]GCCTTTTAACCAATT	4688
rs55900365	snp	A/C	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183574300	AGGGCTCTGCCATCC[A/C]ATACTCTAGGCCTCA	4688
rs57218247	in-del	-/TTTTTTTTTTTTTTT			intron-variant	NCF2	GRCh38.p7	1:183561803	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTT]GAGGCAGAATCTCTC	4688
rs58421758	in-del	-/AAAA			intron-variant	NCF2	GRCh38.p7	1:183585638	CAAAAAAAAAAAAAA[-/AAAA]TTCTTCATTAGCCTG	4688
rs58562761	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183588489	AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAATGAT	4688
rs59044936	snp	A/T	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183588619	ATGAAAATAATTAAA[A/T]TATTATATAAATTGT	4688
rs59470490	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183562589	TCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	4688
rs60311873	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575837	GAAGGATTGATGTTT[C/T]TGTGGCATTAGTGGC	4688
rs60708827	snp	A/G	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183586621	GGACACTGGTGGGGT[A/G]TCACACCAGCTGAGT	4688
rs60826838	snp	A/G	0.0170251	0.090679	intron-variant	NCF2	GRCh38.p7	1:183576550	CACAACCCCTCTCTC[A/G]CCTCTGCTACAATAC	4688
rs61684650	in-del	-/ATG			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555716	TGTTTTTGTAAGATG[-/ATG]CTAGGTTTTTTTTTA	4688
rs61809332	snp	C/T	0.5	0	splice-donor-variant	NCF2	GRCh38.p7	1:183590155	AGGCACCTCCACTCA[C/T]CTTCTCTGCTTCAGT	4688
rs66463680	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183561780	ACCATACCAGGCCTC[-/T]TTTTTTTTTTTTTTT	4688
rs66625837	in-del	-/A			intron-variant	NCF2	GRCh38.p7	1:183571114	GCGTGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	4688
rs66816815	in-del	-/C	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183581298	TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT	4688
rs66977652	in-del	-/T	0.499598	0.0141716	intron-variant	NCF2	GRCh38.p7	1:183571081	AAATTGCACCTCAAT[-/T]AAAAACATTTCTTTT	4688
rs71130625	in-del	-/A	0.476918	0.104919	intron-variant	NCF2	GRCh38.p7	1:183581675	TCTCAAAAAAAAAAA[-/A]CACTTAGCAAGGATG	4688
rs71555411	in-del	-/A	0.5	0	upstream-variant-2KB, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590845	GAAACCCCACCTTCA[-/A]GCCAAAAACAGCCTG	4688
rs71924876	in-del	-/T			intron-variant	NCF2	GRCh38.p7	1:183561642	CTTTCTTTTCTTTTC[-/T]TTTTTTTTTTGTATT	4688
rs72550871	snp	A/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183577795	GTCCCAGTGAAATAG[A/G]TGGGGAAGGGAGAAG	4688
rs72550872	snp	C/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183577838	TGCTGAAAACTAGAA[C/G]AGGTCAAAAGGAACT	4688
rs72550873	snp	C/G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577937	TGTGACTGTCCAAGA[C/G/T]GAGGCACTCAGGGTT	4688
rs72550874	snp	G/T	0.00995	0.0698283	intron-variant	NCF2	GRCh38.p7	1:183574628	GTTGCGGKCTGTACT[G/T]TTCTAGGTGTTATAT	4688
rs72550875	snp	G/T	0.000247078	0.0111121	intron-variant	NCF2	GRCh38.p7	1:183563343	GTTTTTGTGATGATG[G/T]TCTTTGACTGGATTC	4688
rs72550876	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183563366	CTGGAGGAGGGAAGA[A/G]GAGGATGGTTTTTGT	4688
rs72550877	snp	C/T	0.010152	0.0705191	intron-variant	NCF2	GRCh38.p7	1:183564121	GGTTGGGGGCCCTAT[C/T]TGAAGAGGTTTCATC	4688
rs72550878	snp	A/G	0.00636936	0.0560724	intron-variant	NCF2	GRCh38.p7	1:183564194	ATGCTTCCCCAGGGC[A/G]AGATTTTCCCCACAG	4688
rs72550879	snp	G/T	0.01005	0.0701712	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592695	CTACAAATCCATTTG[G/T]TTTTCTCAGGAATAA	4688
rs72550880	snp	C/G	0.000757663	0.0194488	intron-variant	NCF2	GRCh38.p7	1:183586853	GGAGGATTTCAGAGA[C/G]AAACCCAAGGGGTCT	4688
rs72550881	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591706	CTGAGGTCAGGAGTT[C/T]GAGACCATCAGCCTG	4688
rs72550882	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591768	GGCACGGTGGCTCAC[C/G/T]CCTGTAATCCCAGCA	4688
rs73054029	snp	A/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183570715	CACACATAGTCTCTC[A/G]AATTGAATGCTTCAC	4688
rs73054037	snp	C/T	0.00676609	0.0577691	intron-variant	NCF2	GRCh38.p7	1:183580699	ATGTCTACAGAGGCC[C/T]GGTGCAGTGGCTCGT	4688
rs73054039	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581595	CAGCCTCCCAAAGTA[C/G]AAAGACTGCAACTGT	4688
rs74430255	snp	G/T	0.0119091	0.0762411	intron-variant	NCF2	GRCh38.p7	1:183577062	CTTTGAGCAAGAGGG[G/T]ACAGATTTATGCCAA	4688
rs74654158	snp	A/C	0.00159672	0.0282101	intron-variant	NCF2	GRCh38.p7	1:183563337	GAGTAAGAATCCAGT[A/C]AAAGAACATCATCAC	4688
rs75023426	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183565075	TTCAAAATAAAAATG[A/G]GGGAAGGGACATCCC	4688
rs75143113	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560927	GCATCAACTCTAACA[G/T]CAACACTAGGGACCT	4688
rs75392484	snp	A/G	0.000115408	0.00759543	intron-variant	NCF2	GRCh38.p7	1:183573336	TATGTGAAAATGGGG[A/G]TGACGATGCTTGTCC	4688
rs75445762	snp	G/T	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183564969	CAGGGCGAGTTCATG[G/T]TGCAAAATGTTAACA	4688
rs75464378	snp	A/T	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183558233	ACTCTCTCTACCCCC[A/T]TTAACTTTTTTTTTA	4688
rs75889255	snp	G/T	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183571136	TTTTTTTTTTTTTTT[G/T]AGACGGAGTCACGCT	4688
rs76066112	snp	A/C	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183589749	GCAAAGTCGACACAC[A/C]TGAAAGTCTTGGAAA	4688
rs76297529	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183559035	TAGGCTGGCAAACCA[C/T]GAGTTGGAATGGTGC	4688
rs76468779	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183568133	TGAGCTCATCCAGCC[C/T]CCTCATTTTTGTAGT	4688
rs76489392	snp	A/G	0.0517044	0.152246	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591395	TGTATTAATATGTTA[A/G]TGTTTATCTTGAGCT	4688
rs76563165	snp	G/T	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183558276	TTGTTTTTGTTTTTG[G/T]TTTTTTTTTGAGACT	4688
rs77340998	snp	A/C	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183585624	GGCGAAACTCCGTCT[A/C]AAAAAAAAAAAAAAT	4688
rs77777598	snp	A/G	0	0	intron-variant	NCF2	GRCh38.p7	1:183581478	TTCTCTAAAAAAAAA[A/G]AGATTACTTATTTTA	4688
rs77904123	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183577936	CAACCCTGAGTGCCT[C/T]GTCTTGGACAGTCAC	4688
rs78386586	snp	A/C	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183562826	GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAGG	4688
rs78453934	snp	A/C	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183585626	CGAAACTCCGTCTCA[A/C]AAAAAAAAAAAATTC	4688
rs78673263	snp	G/T	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183581676	ATCCTTGCTAAGTGT[G/T]TTTTTTTTTTGAGAC	4688
rs79017889	snp	C/T	0.00835141	0.0640778	intron-variant	NCF2	GRCh38.p7	1:183559092	GCATCACCTGGAAAC[C/T]TGGTAGAAATGCAAG	4688
rs79148462	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183558573	GCACCCGGCCTATTT[C/T]TATTTTTTTTAAGAC	4688
rs79633651	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582808	CTGAAAGACAGCTTC[C/G]AGCCCCTGTGCCTTT	4688
rs80293101	snp	G/T	0	0	intron-variant	NCF2	GRCh38.p7	1:183581686	AGTGTTTTTTTTTTT[G/T]GAGACAGAGTCTCGC	4688
rs111280908	snp	A/G	0	0	intron-variant	NCF2	GRCh38.p7	1:183581294	CTCAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	4688
rs111335841	snp	A/G	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183578576	TCACCATGTTGGCCA[A/G]GCTGGTCTCAAACTC	4688
rs111439551	snp	C/T	0.0150606	0.0854603	intron-variant	NCF2	GRCh38.p7	1:183582904	CTTTTCAGAAATGTG[C/T]TCTAACTTTGTTCTG	4688
rs111447649	snp	A/C	0.00835141	0.0640778	intron-variant	NCF2	GRCh38.p7	1:183576298	CCATTTTAACCCCAA[A/C]TCCAGGGGAAACATT	4688
rs111532709	snp	C/T	0.5	0	missense	NCF2	GRCh38.p7	1:183586959	AGTGCTTGTCTCGGT[C/T]AATGCTTCTGGTAAA	4688
rs111686087	snp	A/G	0.0111196	0.0737302	intron-variant	NCF2	GRCh38.p7	1:183588184	TTTTTGGAGGTGATA[A/G]TGATGTCAAACTTAA	4688
rs111808208	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183587036	GAGGAGGTGTGAGAT[A/G]AGCCACGGCTCACAG	4688
rs111891866	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183574254	TCTCCTGCATTGCCA[A/G]GGAGCCCCACTCCAA	4688
rs111925806	snp	A/G	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183566832	TCCAGGGGTCCTGAC[A/G]ACACCTCTTTTACAC	4688
rs111940286	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183582088	AGCTGCAGCCCTGAA[A/G]GGGGTTCCGCTTTGA	4688
rs112075504	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581823	CAGGCGTCCGCCACC[A/G]CGCCCGGCTAATTTT	4688
rs112296964	snp	C/G	0.0437281	0.141251	intron-variant	NCF2	GRCh38.p7	1:183579688	AGCTTGCAGTGAGCA[C/G]AGATCACACCACTGC	4688
rs112308824	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183586270	GCCTGGGAGGCGGAG[A/G]CTGCGGTGAGCTGAG	4688
rs112321165	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183587022	TGATGCAAGGCAGTG[A/G]GGAGGTGTGAGATGA	4688
rs112336681	snp	C/T	0.5	0	synonymous-codon	NCF2	GRCh38.p7	1:183565777	CTGCGGAGAGCTTTC[C/T]TCCTGAAGGCAACAG	4688
rs112362245	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183559807	GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG	4688
rs112429474	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183586440	ATATAATGTTAATTT[A/G]TATTATCATTTTTGC	4688
rs112516933	snp	C/T	0.0509478	0.151255	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592895	ATTCCTGCATCTGTG[C/T]GACTCGTGCTAGTTC	4688
rs112667828	snp	C/T	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183578038	CAGCTCTCATTCTCT[C/T]TTGAGAGCTCCAAGC	4688
rs112723325	snp	A/G	0.00953873	0.0683987	intron-variant	NCF2	GRCh38.p7	1:183581231	AGACTGCAGTGAGAC[A/G]TGATTGCACCACTCC	4688
rs112923747	snp	A/C/T	0.000100092	0.0070736	intron-variant	NCF2	GRCh38.p7	1:183567399	CACATGATGCCATGG[A/C/T]GCAAATACACTGAAC	4688
rs113168768	snp	C/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183560345	CATCACTAAAGGAAA[C/T]AGCGAAATGTCAAAG	4688
rs113608204	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183587052	AGCCACGGCTCACAG[A/G]GCCCTAGCTCCCTGT	4688
rs113627806	snp	A/G	0.5	0	intron-variant	NCF2	GRCh38.p7	1:183560400	AAGTTTGTGATCAGT[A/G]CCTTGTGTAGAGCTT	4688
rs113692133	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183571493	ACTACTGCCTCTCTC[C/T]AATTCCAAAATATTT	4688
rs113751339	snp	C/G	0.0174175	0.0916809	intron-variant	NCF2	GRCh38.p7	1:183558602	ACAGAGTCTCGCTCT[C/G]TCACCCAGGCTGGAG	4688
rs113805839	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575867	CTGGTGCTGAATGGT[A/G]GGGGCCAGGATCAAC	4688
rs113846676	snp	C/T	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183557191	CCAGTAAAAATCAGA[C/T]AACTTAGGTATGATC	4688
rs113908540	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183589685	TCAGAATTGTCACTT[G/T]GGATAAAAGCTATTT	4688
rs114623469	snp	A/G	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183566013	GAAGAATCCTAACCC[A/G]CTAAAACGCCCTTGC	4688
rs115365142	snp	C/T	0.00159659	0.028209	missense, intron-variant	NCF2	GRCh38.p7	1:183573231	AGCTGAGCCACTTGT[C/T]TCTCATTTGGTCGAA	4688
rs115576005	snp	C/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183570415	GGTTCCCCACTTGCC[C/T]CTGTACTCAAGAAGA	4688
rs115714889	snp	A/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183583520	AGTTCCTTGAAACGG[A/G]GACTATATTTTGCTC	4688
rs116135234	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183583513	ATTTATAAGTTCCTT[A/G]AAACGGAGACTATAT	4688
rs116571614	snp	C/G	0.00557542	0.0525036	intron-variant	NCF2	GRCh38.p7	1:183573659	TGCTCCCTTGGATGG[C/G]TGTTTGCTGATGAGG	4688
rs116630740	snp	A/G	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183561484	ATTCAATGAGATGAC[A/G]TACAATAATAGTAGT	4688
rs117693062	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592222	TACTCCACAGTGCTT[A/G]TAGGATTGAAGGTGT	4688
rs117874531	snp	C/G	0.168785	0.236441	intron-variant	NCF2	GRCh38.p7	1:183580717	TGCAGTGGCTCGTGC[C/G]GGTAATCCCAGCATT	4688
rs119103274	snp	C/T			missense, intron-variant	NCF2	GRCh38.p7	1:183574605	TGTTATATAACATTG[C/T]TTTCATGTATGCCAA	4688
rs119103275	snp	A/G	1.64727e-05	0.00286986	NCF2	1	allele_origin=G(germline)/A(germline)	1:183586922	TGGCTTACTTCCAAC[A/G]AGGGATGCTCTACTA	4688
rs119103276	snp	C/G/T	0.00205726	0.0320062	NCF2	1	allele_origin=T(germline)/C(germline)	1:183577667	AAAGAAGCCTTGATT[C/G/T]AGCTTCGAGGGAACC	4688
rs137854507	snp	C/G			missense	NCF2	GRCh38.p7	1:183577686	TTTGGCTATCAAAGA[C/G]CTTAAAGAAGCCTTG	4688
rs137854508	snp	C/T			missense, intron-variant	NCF2	GRCh38.p7	1:183573189	ATTACCTAGGCAAGG[C/T]GACGGTAGGTGGGAT	4688
rs137854509	snp	A/T			missense	NCF2	GRCh38.p7	1:183577642	GGAACCAGCTGATAG[A/T]CTATAAGATCCTGGG	4688
rs137854510	snp	C/G/T			missense	NCF2	GRCh38.p7	1:183590200	ATTTGCTTCAACATT[C/G/T]GCTGCATGTACACTA	4688
rs137854511	snp	A/G			missense	NCF2	GRCh38.p7	1:183565721	CCAAAGCCCCTGGAA[A/G]ACCCCAGCTGTCACC	4688
rs137854512	snp	A/G/T	4.94176e-05	0.00497059	NCF2	1	allele_origin=G(unknown)/A(germline)	1:183586917	TACTTCCAACGAGGG[A/G/T]TGCTCTACTACCAGA	4688
rs137854513	snp	A/G	0.000164821	0.00907652	NCF2	1	allele_origin=G(germline)/A(unknown)	1:183563507	ATGAAGACTCAGCCC[A/G]GGCTCCCCTACAGCC	4688
rs137854514	snp	A/G			missense	NCF2	GRCh38.p7	1:183590205	CCCGGATTTGCTTCA[A/G]CATTGGCTGCATGTA	4688
rs137854515	snp	A/C/G/T	6.58983e-05	0.00573981	NCF2	1	allele_origin=G(germline)/C(unknown)	1:183577660	CCTTGATTCAGCTTC[A/C/G/T]AGGGAACCAGCTGAT	4688
rs137854516	snp	A/T			missense, intron-variant	NCF2	GRCh38.p7	1:183574579	GCCAAGAAGGAGGAA[A/T]GGAAAAAAGCTGAAG	4688
rs137854517	snp	C/G			missense, intron-variant	NCF2	GRCh38.p7	1:183573289	TCTGTGTTACAGAAG[C/G]AGAAGCTATATGAGC	4688
rs137854518	snp	C/G	3.29451e-05	0.00405851	NCF2	1	allele_origin=G(germline)/C(unknown)	1:183573243	TGGGCAAGCTGTTTC[C/G]ACCAAATGAGAGACA	4688
rs137854519	snp	A/G			missense	NCF2	GRCh38.p7	1:183586919	CTTACTTCCAACGAG[A/G]GATGCTCTACTACCA	4688
rs137854520	snp	A/C			missense, intron-variant	NCF2	GRCh38.p7	1:183574569	AGGAATGGAAAAAAG[A/C]TGAAGAACAGTTAGC	4688
rs137878529	snp	C/T			missense, intron-variant	NCF2	GRCh38.p7	1:183574507	CACACTCCATCGCCT[C/T]GTCGATTTTGGAATG	4688
rs137937390	snp	A/G	0.000576469	0.0169677	missense	NCF2	GRCh38.p7	1:183565766	GGGATGTCGGACTGC[A/G]GAGAGCTTTCCTCCT	4688
rs138208616	snp	A/G	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183572337	TTACAGGCATGCACC[A/G]CAGCACCCAGCTAAT	4688
rs138466536	snp	C/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183565104	CCGAGTGATTCTGAT[C/G]ATCAGGCGCGTGTGG	4688
rs138860204	snp	C/T	0.000312956	0.0125052	missense	NCF2	GRCh38.p7	1:183565725	ACAGCTGGGGTCTTC[C/T]AGGGGCTTTGGAACT	4688
rs138932148	snp	G/T	0.00104057	0.0227861	intron-variant	NCF2	GRCh38.p7	1:183570867	ACAGGAGGGTGTGAG[G/T]CTCTGCCAGCACTGT	4688
rs138950569	snp	A/G	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183559152	GAATCTCTGGAGGGT[A/G]GGCCCAGGAATTGAT	4688
rs139108402	snp	A/C/T	6.59287e-05	0.00574113	missense	NCF2	GRCh38.p7	1:183556131	TCCTAGACTTCTCTC[A/C/T]GAGTGCTTTCCAAAT	4688
rs139128782	snp	C/G	0.00636936	0.0560724	downstream-variant-500B	NCF2	GRCh38.p7	1:183555537	CCTAACTCAGTCTAG[C/G]TTCTGTTTAAGCAAC	4688
rs139387913	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183578526	AGCGCCACCACGCCC[A/G]GCTAATTTTTTATAT	4688
rs139657658	snp	A/C	0.0134861	0.0810011	intron-variant	NCF2	GRCh38.p7	1:183576535	ATGCGCAGGACGCAC[A/C]ACAACCCCTCTCTCG	4688
rs139817332	snp	A/G	0.000153988	0.00877328	synonymous-codon	NCF2	GRCh38.p7	1:183560112	CTTTGATAACACCAG[A/G]ATTATATCCCCTTCC	4688
rs139911935	snp	C/T	0.00557542	0.0525036	intron-variant	NCF2	GRCh38.p7	1:183583517	ATAAGTTCCTTGAAA[C/T]GGAGACTATATTTTG	4688
rs139981019	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592526	CTTTTCATTCTAGGA[A/T]CTCTAGCACAGATAC	4688
rs140028944	snp	A/G	1.65086e-05	0.00287298	stop-gained	NCF2	GRCh38.p7	1:183570788	GCCTTACCTGTGGTT[A/G]CAGAGGGGCAAACCC	4688
rs140037181	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578206	CATCACCCTCCTGCC[C/T]ACTGCCTTCGCCCAT	4688
rs140116475	in-del	-/AAAG			intron-variant	NCF2	GRCh38.p7	1:183581315	AGAAAGAAAGAAAGA[-/AAAG]AAAGAAAGTCCAACA	4688
rs140150135	snp	A/G	0.0119091	0.0762411	intron-variant	NCF2	GRCh38.p7	1:183576131	ATGATGTGATTCTCA[A/G]AAGCCAGGGTCATAC	4688
rs140189189	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575240	TTTGGGAGGCCAAGG[C/T]GGGTGAATCACTTGA	4688
rs140334263	snp	C/T	0.0185938	0.0946107	intron-variant	NCF2	GRCh38.p7	1:183588664	ATACAAACTTATACA[C/T]GAATAGTATACAATT	4688
rs141012108	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586575	GACAGCTCAGTACCT[C/T]ATAGGAGACCTACAT	4688
rs141050774	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585054	TTAGAAAAGACTTCA[C/T]TTCTACTTTCACTTC	4688
rs141063458	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183587995	GATAGAAGCTTTGAG[C/T]CAGTAGACACTATGT	4688
rs141137369	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566577	CATTGTACCAGCCAA[C/T]ACATTGACTACTCTT	4688
rs141378178	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183570202	AATGTGTTTTCCCCT[C/T]TTTCCTTCACAAGGA	4688
rs141538059	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587427	AGTGAGACTCCATCT[C/T]TACGAAAAATTTAAA	4688
rs141569987	snp	C/T	0.000922084	0.0214521	missense	NCF2	GRCh38.p7	1:183560222	CTGTTGTCTGGTTAT[C/T]AGCATCAGCTTTTTC	4688
rs141662379	snp	C/T	0.00517822	0.0506191	intron-variant	NCF2	GRCh38.p7	1:183557812	TTGGAGGTGTTCAAC[C/T]CAGTTCTTCCCACTG	4688
rs142007716	snp	A/G	0.0178098	0.0926698	intron-variant	NCF2	GRCh38.p7	1:183579520	TCACGAGGTCAGGAG[A/G]TCGAGACCATCCTGG	4688
rs142167522	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183557650	CTTAGACTTGTACAG[A/G]TAGGTCATAGTAAGA	4688
rs142362100	snp	C/G	0.00953873	0.0683987	intron-variant	NCF2	GRCh38.p7	1:183560592	TTAGATTCTCATAAA[C/G]AGCATGCGACCTAGA	4688
rs142534060	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183581243	GACATGATTGCACCA[C/T]TCCACTCCAGCCTGG	4688
rs142633260	snp	C/T	0.000153988	0.00877328	missense	NCF2	GRCh38.p7	1:183560200	CTGCCTTTCTTAAGC[C/T]GAGGTTCTGTTGTCT	4688
rs142803799	snp	A/C/T	0.000329407	0.0128297	missense	NCF2	GRCh38.p7	1:183586955	GCCAAGTGCTTGTCT[A/C/T]GGTTAATGCTTCTGG	4688
rs142827935	snp	A/G	0.00398564	0.0444627	intron-variant	NCF2	GRCh38.p7	1:183577905	ATGGTGTTCCCCCCA[A/G]GGCTGTGCCTCAAAG	4688
rs143178891	snp	A/G	8.23621e-05	0.00641672	synonymous-codon	NCF2	GRCh38.p7	1:183586909	CTTCTCTGTCTGGTA[A/G]TAGAGCATCCCTCGT	4688
rs143279907	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591010	TCCAGTACTACCTAT[A/G]TCCTGCCCCTCCCCT	4688
rs143404496	snp	C/T	0.00676609	0.0577691	intron-variant	NCF2	GRCh38.p7	1:183576504	AAAAGCTAGAGATGC[C/T]GTCAAAGTTCCCACG	4688
rs143582889	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578215	CCTGCCCACTGCCTT[C/T]GCCCATGGCTTCTTT	4688
rs143617544	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183584749	ACGGGGTAAGGGGGA[A/G]TGAGAAAGAGAAGGA	4688
rs143687872	in-del	-/TGAG/TGAGTGAG	0.040671	0.13668	downstream-variant-500B	NCF2	GRCh38.p7	1:183555429	ATATATATTCAGTAT[-/TGAG/TGAGTGAG]TGAGTTCTTAACACA	4688
rs143704221	snp	A/G	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183572507	TTTAGAAGAAGTCCA[A/G]TTTAAGACATAGTCT	4688
rs143726411	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183588899	GAGGCTACAGTCCCT[A/G]CTGGCATAGCTGTGC	4688
rs143756957	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183575343	GGCATGGTGGCAGGC[A/G]CCTGTAATCTCAGCT	4688
rs143879468	snp	A/G	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183566177	AAAGCATTTGGATAT[A/G]GTGACTGACCAGGGA	4688
rs143889676	snp	A/G	0.000280017	0.0118292	synonymous-codon	NCF2	GRCh38.p7	1:183590237	GTGGGGGTCCTGGAC[A/G]GCACTGAAGGCATCC	4688
rs143901397	snp	C/G	0.00111993	0.0236371	missense	NCF2	GRCh38.p7	1:183556147	GAGTGCTTTCCAAAT[C/G]TGTAGTTGCGCAGTC	4688
rs143986901	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556669	CCCAAGTAACTGCAA[C/G]TACAGGCTGTGCCAC	4688
rs144224639	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183584199	GGACTTCATATCTAT[A/G]GCCCCTGAATTGTAC	4688
rs144451516	snp	A/G	9.88321e-05	0.00702896	missense	NCF2	GRCh38.p7	1:183569163	ATCTCTGGGGTTTTC[A/G]GTCTGGGTGGAGGCT	4688
rs144514762	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591196	CAGCAGGTAGTGTGG[C/T]CCACTGAGGCCTGGG	4688
rs144591832	snp	A/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183562356	CTGGAAAACCTAGAG[A/T]GACTTTTCAGACTTC	4688
rs144819622	snp	C/G/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183583621	AGTAAAGATTTCTTA[C/G/T]GAAATTCGTAGAGTA	4688
rs145087251	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565632	TTTCCTGGAAGGCAG[A/G]GAGAGGAACTCAGGA	4688
rs145099974	snp	A/G	0.0185938	0.0946107	intron-variant	NCF2	GRCh38.p7	1:183587536	GAGGTGGAGACTGCC[A/G]TGAGCTGTGACGGCA	4688
rs145120066	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570238	TGTGTGCATTTCTAG[A/G]TCCACTATCATCCAG	4688
rs145229115	snp	C/T	0.00212288	0.0325105	missense	NCF2	GRCh38.p7	1:183563301	TTGCTGTCCCGAGGC[C/T]GATAGCTGGGTGGGG	4688
rs145354685	snp	A/G	0.000115309	0.00759218	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573283	CCACTGGCTCATATA[A/G]CTTCTGCTTCTGTAA	4688
rs145441637	snp	A/G	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183584349	CACCTAGGGAATTGC[A/G]CAAGAGGGCCTGCTT	4688
rs145455213	in-del	-/AA	0.0174175	0.0916809	intron-variant	NCF2	GRCh38.p7	1:183589647	AGCCTCAGCATCTTT[-/AA]AAGAGTCTCCTTTAT	4688
rs145542661	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183582660	GGCTGCTGTGACAGA[-/G]GGTTTGGGCCCACTC	4688
rs145970396	snp	A/G	1.6473e-05	0.00286988	missense	NCF2	GRCh38.p7	1:183563296	GCTCATTGCTGTCCC[A/G]AGGCCGATAGCTGGG	4688
rs146187702	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	NCF2	GRCh38.p7	1:183555408	ATCACTTAAATGTTG[A/G]CGATTGATATATATT	4688
rs146762552	snp	A/G	6.58957e-05	0.00573964	synonymous-codon	NCF2	GRCh38.p7	1:183560118	TAACACCAGGATTAT[A/G]TCCCCTTCCTGAAAC	4688
rs146871378	snp	G/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183575275	AGGAGTTTGAGATCA[G/T]CCTGGCCAACATGGA	4688
rs146921044	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183572093	CTGGGCAACTTTAGC[A/C]CTATGAATGTGTCAA	4688
rs146937130	snp	A/G	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183576143	TCAGAAGCCAGGGTC[A/G]TACCACATCAGGAAG	4688
rs146967039	snp	A/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183578972	CAGTCCCCTGACCTG[A/G]CAGGAACAAATTTGG	4688
rs147070509	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558221	CACTTGTTGTATACT[C/T]TCTCTACCCCCATTA	4688
rs147180870	snp	A/G	8.24083e-05	0.00641852	intron-variant	NCF2	GRCh38.p7	1:183566897	GGTGAGAGGAAATGG[A/G]TCAGGCCTTGGCATC	4688
rs147415774	snp	C/T	0.00289511	0.0379364	missense	NCF2	GRCh38.p7	1:183590217	ATGTTGAAGCAAATC[C/T]GGGAGTGGGGGTCCT	4688
rs147531878	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591036	CCCCTATTCTGAGCC[C/T]ATAAAAGCCCCAGAC	4688
rs147599741	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183583622	GTAAAGATTTCTTAC[A/G]AAATTCGTAGAGTAG	4688
rs147657171	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183573185	AGCAATCCCACCTAC[C/T]GTCGCCTTGCCTAGG	4688
rs147687207	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183558695	TCAGCCTCCCTAGCA[G/T]CTGGGACTACAGATG	4688
rs147744729	snp	A/T	0.00373535	0.0430549	missense	NCF2	GRCh38.p7	1:183563531	TCTTCATGACTACCG[A/T]GTACTTGTAGTGCAC	4688
rs147908264	snp	C/T	0.00458709	0.0476708	missense	NCF2	GRCh38.p7	1:183563455	TTAGTGTGTTCCAGC[C/T]GGAGCTCCAGTTTCT	4688
rs148005568	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	NCF2	GRCh38.p7	1:183563285	AAGGGGCACCAGCTC[A/G]TTGCTGTCCCGAGGC	4688
rs148058176	in-del	-/ATC			intron-variant	NCF2	GRCh38.p7	1:183571112	GTATAACATCAAATT[-/ATC]TTTTTTTTTTTTTTT	4688
rs148058862	snp	A/G	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183584974	AGAGCTAAATGCCTG[A/G]ATATCTTCTCCCAAT	4688
rs148112860	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183589060	AGCCAGAGGTGGGGG[A/G]TCCTGCCATGCTCTG	4688
rs148202357	snp	C/T	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183566251	CAGTCTCCACTGCCA[C/T]TGAGTCACTTACAGG	4688
rs148539738	snp	C/T	0.00398564	0.0444627	intron-variant	NCF2	GRCh38.p7	1:183577877	TCCAAGTATTCTATA[C/T]AACTCCTTGGGAATG	4688
rs148679662	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557398	ACTGTCTTGATTCTT[C/T]TTACAGGGTAGGTCG	4688
rs148819724	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183584641	TAGACTATTAGAGGT[C/T]ACTAAGGAATGACCT	4688
rs148855262	snp	C/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183578693	TTCTAATGCTGCTCC[C/T]ACTGCCTTGTGCTGC	4688
rs148936339	snp	A/C	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183568131	AATGAGCTCATCCAG[A/C]CCCCTCATTTTTGTA	4688
rs148992445	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575342	GGGCATGGTGGCAGG[C/T]ACCTGTAATCTCAGC	4688
rs149255017	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183571585	TAAACTGGCAACAAC[C/T]GGTTTGCTTTCTGTG	4688
rs149418882	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183559594	CCAGGTGCGGTGGCT[C/T]ATGCCTGTAATCTCA	4688
rs149476369	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183566029	CTAAAACGCCCTTGC[C/T]GCTTTAGCAACTCTT	4688
rs149613627	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591139	TGTTTTCATCACTCA[A/G]TAAAACTCCCCACCC	4688
rs149735720	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183560965	AATGCAGACTTTCAA[C/T]TCCATCCCAAAACTA	4688
rs149789558	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183567744	GAAGTCAGGTGAGAG[A/C]CAGCTGGGCCAGAAA	4688
rs149874973	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183587524	GCTCAAGCCCAGGAG[A/G]TGGAGACTGCCGTGA	4688
rs149984119	snp	A/C	0.00914312	0.0669923	intron-variant	NCF2	GRCh38.p7	1:183574096	CTCCATCTCAAAACA[A/C]AACAAAACATTTTTG	4688
rs150037197	snp	A/G	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183578531	CACCACGCCCGGCTA[A/G]TTTTTTATATTTTAA	4688
rs150121162	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183571439	ATCATTTTAAAGTGA[A/G]TGATTCAGTGGCATT	4688
rs150182900	snp	A/G	0.00199481	0.0315187	utr-variant-5-prime, intron-variant, upstream-variant-2KB	NCF2	GRCh38.p7	1:183590593	GAGAGAGGGCGAGTA[A/G]GGGTGGAGTGTGGAG	4688
rs150496854	snp	A/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183560831	TACTGAAACCTTACA[A/G]TAATCTTGAGACAGG	4688
rs150595188	snp	C/T	0.000510528	0.0159688	missense	NCF2	GRCh38.p7	1:183569152	CTTACCTGAAGATCT[C/T]TGGGGTTTTCGGTCT	4688
rs150809838	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566830	TCTCCAGGGGTCCTG[A/C]CAACACCTCTTTTAC	4688
rs150829258	snp	C/G	0.00478085	0.0486577	intron-variant	NCF2	GRCh38.p7	1:183586032	GAACTGTTTTGAAAT[C/G]TGTTTTTAAATTTAA	4688
rs150863818	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573620	CGACAAGGCTGGCCC[A/G]GGATCAAGCAAGGCT	4688
rs150901160	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587593	AGTAAGGCACCCTGT[C/T]TCAAAAAAAAAAAAA	4688
rs151163633	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183587295	GGCCTAGAAAAGCTA[C/T]ACAAGAATCCAATAA	4688
rs151172473	snp	C/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183575441	ACCTTCACCTCAGGT[C/G]GGGGGGGAATGGTAA	4688
rs151187727	snp	A/G	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183557671	CATAGTAAGACGCAT[A/G]CTGGCTTCTCTCCAT	4688
rs180831437	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183558597	TTAAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC	4688
rs180890007	snp	C/T	0.00953873	0.0683987	intron-variant	NCF2	GRCh38.p7	1:183581174	GTAGTCCCAGCTACC[C/T]GGGAAGCTGAGGTTG	4688
rs181093436	snp	C/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183557444	TTAGAAATGAAAAAT[C/G]CCAGATCCAAACCAG	4688
rs181102454	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580839	TAAAAATTAGCCGGG[C/T]GTGGTGGTGCGTGCC	4688
rs181107462	snp	A/C	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183571067	TTCTTCTCTCTTAAA[A/C]AAGAAATGTTTTTAA	4688
rs181315724	snp	A/C/G	0.0107246	0.0724382	intron-variant	NCF2	GRCh38.p7	1:183563896	GGTAGCAACTGGTTC[A/C/G]ACCCTCCCTTTGGGG	4688
rs181323554	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555112	CTCTATGTTTGTTTA[C/T]ACTGATGATACTTAC	4688
rs181462025	snp	G/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183576373	TTTCTAGAGCCACTT[G/T]TCCCCCAACTTTCTA	4688
rs181583220	snp	A/C	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183575979	CCAGCCCACTCCTGA[A/C]CTTGTGTGCAGAAAG	4688
rs181642750	snp	C/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183564839	ATGTTTAGTGTCCTA[C/G]ATACCATGATTCTAT	4688
rs181715462	snp	A/G	0.0111196	0.0737302	intron-variant	NCF2	GRCh38.p7	1:183586227	TAGTCCCAGCTACTC[A/G]GGAGGGTAAGCCAGG	4688
rs181735066	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183564201	GAAAATCTCGCCCTG[A/G]GGAAGCATGAAGGTC	4688
rs181748866	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183585845	TTGAATTTATTAATC[G/T]TTGTACTAATTATTC	4688
rs181922430	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559184	TAACAAACTCTTCCA[A/G]GGATTCTTAGAACTC	4688
rs181948236	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577148	ATAGTAAAGAGTGTG[A/G]TCTATAAACTTGGGA	4688
rs181949612	snp	A/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183581473	ACCCCTTCTCTAAAA[A/G]AAAAAAGATTACTTA	4688
rs182190053	snp	A/G			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591842	ACCAATTTCCTGCAA[A/G]TGTCAAAATTGGGAG	4688
rs182237269	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183562044	AGGCATGAGCCACTG[C/T]GCCTGGTTTTCTTTC	4688
rs182243285	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183582546	GCTGCCAGTGCCCCA[C/T]GCGTCCAGAGTCCAC	4688
rs182449012	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183569793	AGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	4688
rs182453292	snp	A/C	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183588427	TTGCAGTGAGCCGAG[A/C]TTGCACCACTGCACT	4688
rs182494030	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183571487	TGTGCAACTACTGCC[G/T]CTCTCTAATTCCAAA	4688
rs182744353	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183565989	TGAAAATGAAAATCA[C/T]AGTAGAAAGAAGAAT	4688
rs182762369	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183587861	ACTAATAAAAAATAC[A/G]TATCTATATTTAAAA	4688
rs182819269	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555890	CCATCCACTTTTCCT[C/G]TCCCCTAACTCCTCC	4688
rs182831129	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183577313	AAGCCAACACACTCG[C/T]GTCCAGCCTCCCTTC	4688
rs183005487	snp	A/G	3.29603e-05	0.00405944	intron-variant	NCF2	GRCh38.p7	1:183566900	GAGAGGAAATGGGTC[A/G]GGCCTTGGCATCACA	4688
rs183031007	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183573619	ACGACAAGGCTGGCC[C/T]GGGATCAAGCAAGGC	4688
rs183100144	snp	C/T	3.29554e-05	0.00405914	missense	NCF2	GRCh38.p7	1:183556158	AAATCTGTAGTTGCG[C/T]AGTCTTCAACAAAAA	4688
rs183100548	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555184	ACATGCTGTACAGGT[C/T]TGTAGCCTAGGAGTA	4688
rs183112085	snp	C/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183560348	CACTAAAGGAAACAG[C/T]GAAATGTCAAAGTAG	4688
rs183285261	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578078	ACCTGCCCCCTGCCT[A/G]TGTCCCTGCAGAGTG	4688
rs183377431	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567995	GGCTGGTGTTCAGGT[C/T]TCAGGCTTCCCTCCC	4688
rs183510217	snp	A/C	6.59098e-05	0.00574026	intron-variant	NCF2	GRCh38.p7	1:183564072	CAAAAGAAGATGGTG[A/C]ATGAACATCCTTGGC	4688
rs183513058	snp	A/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183589032	AGAGGAGGTGGGGCC[A/T]TGTCCTTCCTCCAGC	4688
rs183590051	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183581769	CGCCTCCCGGTTCAC[A/G]CCATTCTCCTGCCTC	4688
rs183956204	snp	A/G	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183579602	AAATTAGCTGGGCAT[A/G]GTGGTGGGCGCCTGT	4688
rs183958779	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183556921	CATTGGTTAAATATA[C/T]TAAAAATGAAAGTTC	4688
rs183996746	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183568630	CTTCTTCAGAAAGCA[C/T]GTGCCGATAGGGAGT	4688
rs184020650	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590424	CTGCCTTAGTGGCCC[C/T]CAAGGTGTTCACTTT	4688
rs184130919	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572684	TCAATCTGTTGCCCA[A/C]GCTAGAGTACAGTGG	4688
rs184391488	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183557136	TTTACTAAGGAAAAG[A/G]AGACCCAGAGAGATG	4688
rs184410994	snp	A/G	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183580423	AGCCTCTTCCATCGC[A/G]AAGAGGACAGGCAGA	4688
rs184450964	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591639	AGAAGCCTGCCACCA[C/T]GCCCTGCTAATTTTT	4688
rs184588496	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183569300	CAGAAAATCAAATAA[C/T]GCATTTCTGACTGAT	4688
rs184796314	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557474	GAGTCAGAATCCATT[C/T]AGGAAGATTCGCAGG	4688
rs184924864	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183580893	GTGAGGCAGGAGAAT[C/T]ACTTGAACCCAGGAG	4688
rs184937641	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183584710	TTTGTTGTTAGGCCT[C/G]CCTGCATATTCTATA	4688
rs185114555	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566071	GGAAATCCACTGGCC[A/G]TGGGGCAGGACTGAG	4688
rs185137589	snp	C/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183587948	TTTCATTTCTATTAT[C/T]GCTGTTTTAATAATA	4688
rs185201474	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183581227	GTCAAGACTGCAGTG[A/C]GACATGATTGCACCA	4688
rs185482181	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563823	TTGGGTAGTAGGAAG[A/T]GTGTGCATGATAGTG	4688
rs185658357	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571195	TGATCTCAGCTCACT[A/G]CAACCTCTGCCTTCC	4688
rs185681641	snp	A/T	0.00716266	0.059414	intron-variant	NCF2	GRCh38.p7	1:183581712	CTCGCTCTGTTGCCC[A/T]GGCTGGAGTGCAGTG	4688
rs185711786	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183575311	CCTGTCTCTACTAAA[A/T]ATACAAAAATTAGCT	4688
rs185852100	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183576681	CTCAGACTGTGAGAC[A/G]TGAAGTTAGTTGCTA	4688
rs185965011	snp	A/T	0.000798403	0.0199641	downstream-variant-500B	NCF2	GRCh38.p7	1:183555124	TTACACTGATGATAC[A/T]TACTTACCATTGTGG	4688
rs186209070	snp	A/G	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183585967	ATAACATTTTGATCT[A/G]TGGCCTTCCAGACTT	4688
rs186212401	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575982	GCCCACTCCTGACCT[C/T]GTGTGCAGAAAGAAA	4688
rs186226188	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577181	TGAGCAAGCTTCTGG[C/T]AGGTCCTGCACGGAC	4688
rs186226633	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555248	GGCTATACCATCTAG[C/T]CTTGTGTAAGTGCAC	4688
rs186233916	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571501	CTCTCTCTAATTCCA[A/G]AATATTTTCATCACC	4688
rs186850514	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183562978	TTCTGTGAGCTCCTG[C/T]CCTGCTGGGCCTGCT	4688
rs186857454	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183559264	AACTCCTGGCCTCAA[A/G]TGATCCTCCTACCTC	4688
rs186861350	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183582994	GGGAAATAGAGGGGG[A/G]AAAACCTCCATCCAT	4688
rs186908575	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586835	ACCAAGCCCGCAACA[C/T]TGAGACCCCTTGGGT	4688
rs186921021	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573844	CCTGTAATCCCTGCA[A/C]TTTGGGAGGCCAAGG	4688
rs187112583	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183565015	TGAAAGATATTCTGA[C/T]GTTTATTGTATTCTA	4688
rs187214263	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183572953	TGTGAGTAACCCTGT[A/G]GCTCTCACCCAGGGT	4688
rs187217973	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564344	TAAGCCCACGGGATC[C/T]AAAGCAATGAAAATC	4688
rs187428004	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183577779	ATAAAATGTGAGTCT[G/T]CTTCTCCCTTCCCCA	4688
rs187450678	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183578554	TATTTTAAGTAGAGA[C/T]CAGGTTTCACCATGT	4688
rs187489898	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556034	ACTGTAATGTCTCAG[C/T]ACAGTATACAGCAGA	4688
rs187693381	snp	C/G	0.00478085	0.0486577	intron-variant	NCF2	GRCh38.p7	1:183556368	GAAAAGACAGTATTG[C/G]AAAGTGGTTTGAGAG	4688
rs187807528	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183556973	CACTGAACTCCATTA[A/T]ACAGGTGAGCTGGAG	4688
rs187815708	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183579961	TTTACTTAAAGCTCC[A/G]TGCCATATAAGCTAT	4688
rs187964606	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561244	ATTAGAAATGCTGCT[A/G]GGCTTGTATGTACCG	4688
rs188165376	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585802	TGTGCAGGATGAGAG[A/G]GAGGAGGAATTGAGA	4688
rs188243183	snp	C/T	0.00874735	0.0655527	intron-variant	NCF2	GRCh38.p7	1:183581916	TCGTGATCCGCCCGC[C/T]TCGGCCTCCCAAAGT	4688
rs188623417	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183576123	CAAAAATAATGATGT[A/G]ATTCTCAGAAGCCAG	4688
rs188693904	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590910	AACCCGTGACCTAGA[C/G]TGAGAACTTCTGTTC	4688
rs188731990	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568177	TTGTCACTTTTTTTT[C/T]TTTGAGACGGAATCT	4688
rs188770777	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567759	CCAGCTGGGCCAGAA[A/G]GATTGGTGGGAGAGG	4688
rs189075586	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570451	TGTTAATAAGCCTTC[C/T]ATAGCTTGTGTTTCA	4688
rs189168800	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580481	TGCAATTTCCACTGT[G/T]TTCTATTGCCTGTTT	4688
rs189495668	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563871	GGTCCCTAGCTCATG[A/G]ACTCTGTAAGGTAGC	4688
rs189540801	snp	C/T	0.00200836	0.0316251	intron-variant	NCF2	GRCh38.p7	1:183574638	TAGAAAAGTACAGAC[C/T]GCAACATAAAACTTG	4688
rs189617003	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183575610	ACTGAAATAAATTTT[A/T]TAAATAGGATATTAT	4688
rs189759864	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580939	AGCCAAAACCATGCC[A/G]CTGCACTCCAGCCTG	4688
rs189763283	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183585468	GTCTCTACTGAAAAA[C/T]ACACAAATTAGCTGG	4688
rs189877222	snp	A/G	0.000362659	0.013461	intron-variant	NCF2	GRCh38.p7	1:183566872	CCCCTCCAGGGAGAG[A/G]TCCCTAAAGGGTGAG	4688
rs189885136	snp	C/G/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183588224	TCCTATCCAACACAA[C/G/T]AGAGCACCTTGTCCA	4688
rs190011161	snp	A/C			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592322	CTTCTTTGCCTGGCA[A/C]ACTCCTACTCATCTT	4688
rs190014461	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183557586	TGTCCTACCCTGACC[A/G]CTAAATTCTGTTTTC	4688
rs190063971	snp	A/G	0.00398564	0.0444627	intron-variant	NCF2	GRCh38.p7	1:183557264	TGTCTTTGTACATCT[A/G]GATCAGACATTAAGG	4688
rs190106191	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565270	ATTTCACATCTGCCC[A/G]TTGGTTCTTTGTTCA	4688
rs190318522	snp	A/G	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183569648	GGCTGGAGTGCAGTG[A/G]CGCGATCTTGGCTCA	4688
rs190438099	snp	A/G	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183571280	CCGCCACTGTGCCCG[A/G]CTAATTTTTGTATTT	4688
rs190562314	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183586063	CATCTGGCTGGGCGT[A/G]GTGGCACATGCCTGT	4688
rs190753116	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183581390	AGTTCCAGCTACTCC[A/G]CCAGAGGCTGGGGCA	4688
rs190786502	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555148	ATTGTGGTATAGTTG[C/G]CTGCAGAATTCAACA	4688
rs190839978	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183558614	TCTGTCACCCAGGCT[A/G]GAGGGCAGTGGTGCA	4688
rs191043773	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576727	GGGATGGGGCCATAT[A/G]TCCCCAGGGGCCGAG	4688
rs191067796	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183577950	TCGTCTTGGACAGTC[A/G]CAGGGAGTTTCTTCT	4688
rs191077902	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577311	ACAAGCCAACACACT[C/T]GTGTCCAGCCTCCCT	4688
rs191086499	snp	A/T	0.00119737	0.0244387	downstream-variant-500B	NCF2	GRCh38.p7	1:183555396	CCGCTGCTTTTCATC[A/T]CTTAAATGTTGGCGA	4688
rs191249861	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569254	GGAGAGACAACAAAC[A/G]GCTAATGGTAATTTG	4688
rs191257959	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591011	CCAGTACTACCTATG[A/T]CCTGCCCCTCCCCTA	4688
rs191291244	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183582419	CAGGGGATCCACCAG[C/T]TGAAGCAGCAACCTT	4688
rs191296619	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587755	ATCATTTTAAAAATG[G/T]ACTTGACAATATGAA	4688
rs191488901	snp	C/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183589741	TTGAGCAGGCAAAGT[C/T]GACACACATGAAAGT	4688
rs191529432	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561733	GATCTGGCCCATCTC[A/G]GCCTCCCAAAGTGCT	4688
rs191567387	snp	A/G/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183568369	ATGGGGTTTTGCCAC[A/G/T]TTGGCCCGGCTGGTC	4688
rs191596593	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183560308	GTTAATTTTCCCAAT[C/T]TCCTGCCAAGTGAAC	4688
rs191818519	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183574077	GCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA	4688
rs191855252	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571627	CCCTCTTCTCTGAGT[A/T]TTAAAAATCAGATGT	4688
rs192275739	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556800	TCCCAAAGTGCTGTG[A/G]TGATAGGGGTGAGCC	4688
rs192417377	snp	A/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183562994	CCTGCTGGGCCTGCT[A/G]TTCTCTTGTGGGAAA	4688
rs192438234	snp	A/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183584629	ATCTCTTCTTTATAG[A/T]CTATTAGAGGTCACT	4688
rs192496685	snp	G/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183564449	TGTATGTTTCCTAAA[G/T]TTTATTAATTTAATC	4688
rs192622070	snp	A/C	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183557096	AATATATTCAGACTT[A/C]ATAATAACTTGTAGG	4688
rs192630495	snp	A/G	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183580086	TCATAAGGAACGGGT[A/G]CCAGTGTGGCTGGGG	4688
rs192677031	snp	A/G	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183579313	GGAGCTTGCCAGCAT[A/G]TGGATCCCACTTCTG	4688
rs193003167	snp	G/T	0.00279162	0.0372561	intron-variant	NCF2	GRCh38.p7	1:183575089	TGAAACACTGGACAG[G/T]TACAGAGCCGGAAGA	4688
rs193129881	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588650	TATATTTGTTTACTA[C/T]ACAAACTTATACATG	4688
rs193283181	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183567848	GTAGGTGACAGGGAG[C/T]GTGAGGGATGCACAT	4688
rs199643087	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183558773	TTTCACCATGTTGGC[A/C]AGGTTGGTCTTCAAC	4688
rs199658789	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	NCF2	GRCh38.p7	1:183565713	ACTCACCTGGTGACA[A/G]CTGGGGTCTTCCAGG	4688
rs199728796	in-del	-/AAG			utr-variant-5-prime, intron-variant, upstream-variant-2KB, cds-indel	NCF2	GRCh38.p7	1:183590566	TGAGAGAGAAAAGGA[-/AAG]AAGCAGAGAGAGAGA	4688
rs199788941	snp	C/G	0.00199792	0.0315431	intron-variant	NCF2	GRCh38.p7	1:183567166	ATTTGCTGCCAGGAT[C/G]CCATGCCCATCGCAC	4688
rs199846623	snp	C/G	1.6473e-05	0.00286988	intron-variant	NCF2	GRCh38.p7	1:183574468	ATCCTCTCAACACCT[C/G]CATCACCAATACGCT	4688
rs200105496	in-del	-/A	0.0185938	0.0946107	intron-variant	NCF2	GRCh38.p7	1:183558456	ATTTGTAGCAGAGAC[-/A]AGAGTTTCACCATGT	4688
rs200240164	snp	A/G/T	1.64988e-05	0.00287213	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556116	GTAGTTTGTGAAACA[A/G/T]CCTAGACTTCTCTCC	4688
rs200286542	snp	C/T	1.64735e-05	0.00286993	missense	NCF2	GRCh38.p7	1:183577627	AGCTTGAACTGGAGC[C/T]CCAGGATCTTATAGT	4688
rs200287180	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183556861	AGAGAATTTTACCTG[C/T]GCTTTGTTGGGAATC	4688
rs200423742	snp	G/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555624	CCTATAAGGTTACTT[G/T]AAGCCTTAAGAGCCA	4688
rs200435109	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183589302	GGTGTGAAGTTCCAC[-/G]AGACATTAATAGTTT	4688
rs200530075	in-del	-/AA			intron-variant	NCF2	GRCh38.p7	1:183587440	CTCTACGAAAAATTT[-/AA]AAATTAGTCAGATGT	4688
rs200571242	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564254	TCTCTGCTTCTAGGG[A/G]GCCTATAGGTAATTA	4688
rs200655126	snp	A/G	0.000115316	0.00759243	synonymous-codon	NCF2	GRCh38.p7	1:183565759	AGGAGCTGGGATGTC[A/G]GACTGCGGAGAGCTT	4688
rs200692369	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183571112	GTATAACATCAAATT[A/T]TCTTTTTTTTTTTTT	4688
rs200714564	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183558832	GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA	4688
rs200736155	snp	C/G	0.000510561	0.0159693	intron-variant	NCF2	GRCh38.p7	1:183563970	AAGCTATCCCATCTT[C/G]TACCACTTGAAACAG	4688
rs200824291	snp	A/G	0.000164723	0.00907383	missense	NCF2	GRCh38.p7	1:183590218	TGTTGAAGCAAATCC[A/G]GGAGTGGGGGTCCTG	4688
rs200883341	snp	A/C			downstream-variant-500B	NCF2	GRCh38.p7	1:183555503	TCTCTGTGGAATTGA[A/C]TGTTGTAGTCCATGA	4688
rs201003183	snp	A/T	0.00031294	0.0125049	missense	NCF2	GRCh38.p7	1:183586908	ACTTCTCTGTCTGGT[A/T]GTAGAGCATCCCTCG	4688
rs201050705	snp	A/G			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555856	CTGGAAGACTCTCTC[A/G]TGCCCTTTCCAGACA	4688
rs201081034	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580613	TTCAGCTGGGAAGTG[A/G]CACCACCTGGGTCTA	4688
rs201325416	snp	G/T	1.64789e-05	0.0028704	missense	NCF2	GRCh38.p7	1:183563447	ACCTCAGCTTAGTGT[G/T]TTCCAGCCGGAGCTC	4688
rs201449237	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183581025	GCCTGGTAGGAGAGA[C/G]AGAGAAAGAACTGAC	4688
rs201589700	snp	A/G/T	4.94355e-05	0.00497149	missense	NCF2	GRCh38.p7	1:183590280	CAGTCCTTCTTGTCC[A/G/T]CTGCCAGCACCCCTT	4688
rs201812907	in-del	-/ACT			intron-variant	NCF2	GRCh38.p7	1:183589993	AAACTGGCTGCCTGG[-/ACT]GGCCCCTCCCAGACC	4688
rs201848208	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570874	GGTGTGAGGCTCTGC[C/T]AGCACTGTTTCCATT	4688
rs201869337	snp	C/T	6.58946e-05	0.0057396	missense	NCF2	GRCh38.p7	1:183590236	AGTGGGGGTCCTGGA[C/T]GGCACTGAAGGCATC	4688
rs201901727	snp	C/G/T	8.25844e-05	0.00642543	intron-variant	NCF2	GRCh38.p7	1:183567177	GGATCCCATGCCCAT[C/G/T]GCACCAGCCCCTGAT	4688
rs201995279	in-del	-/CCT			intron-variant	NCF2	GRCh38.p7	1:183580470	TCCTGGCAGCTGCAA[-/CCT]TTTCCACTGTGTTCT	4688
rs202190154	in-del	-/T			downstream-variant-500B	NCF2	GRCh38.p7	1:183555505	CTGTGGAATTGAGTG[-/T]TTGTAGTCCATGAGA	4688
rs202202602	in-del	-/AC			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555745	TTTTATTGTGGTATG[-/AC]ACAGAAAAGTGCACC	4688
rs267606912	snp	A/T			missense, intron-variant	NCF2	GRCh38.p7	1:183574509	GACATTCCAAAATCG[A/T]CAAGGCGATGGAGTG	4688
rs367559644	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556290	GAAGATTACCCTGTC[C/T]GGCTATTCCACACAG	4688
rs367607691	in-del	-/AAAAAAAAAG			intron-variant	NCF2	GRCh38.p7	1:183581300	AAAAAAAAAAAAGAA[-/AAAAAAAAAG]AGAAAGAAAGAAAGA	4688
rs367657316	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561467	AAATTGAGGCTAGAA[A/G]AATTCAATGAGATGA	4688
rs367663802	in-del	-/TC	0.00993419	0.0697739	downstream-variant-500B	NCF2	GRCh38.p7	1:183555539	TAACTCAGTCTAGGT[-/TC]TGTTTAAGCAACAAG	4688
rs367905587	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560878	ATTTCTTTACAGATG[A/G]GGACAGAGCCCTAAG	4688
rs367946786	snp	G/T			utr-variant-3-prime	NCF2	GRCh38.p7	1:183556021	TTAACACTTCCAAAC[G/T]GTAATGTCTCAGTAC	4688
rs368017482	snp	A/C/T	1.64814e-05	0.00287061	intron-variant	NCF2	GRCh38.p7	1:183566899	TGAGAGGAAATGGGT[A/C/T]AGGCCTTGGCATCAC	4688
rs368036315	in-del	-/A	0.356811	0.226034	intron-variant	NCF2	GRCh38.p7	1:183588474	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	4688
rs368088445	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563925	GGCTCTTCCTATAAT[A/C]CAGACAGACATGTCT	4688
rs368121646	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183561499	ATACAATAATAGTAG[C/T]TGACATTTATTGAAC	4688
rs368136871	snp	A/G	0.000214219	0.0103472	intron-variant	NCF2	GRCh38.p7	1:183563425	CACAGCTGCCTGCAT[A/G]GAGCTCACCTCAGCT	4688
rs368172858	snp	A/G	3.29457e-05	0.00405854	intron-variant	NCF2	GRCh38.p7	1:183574442	TCTGAGACAAATGAG[A/G]ATCCAGTGACATCCT	4688
rs368373468	snp	A/G	3.29478e-05	0.00405867	intron-variant	NCF2	GRCh38.p7	1:183563338	AGTAAGAATCCAGTC[A/G]AAGAACATCATCACA	4688
rs368417422	snp	C/T	3.29462e-05	0.00405857	intron-variant	NCF2	GRCh38.p7	1:183574480	CCTGCATCACCAATA[C/T]GCTTACCCAGACACA	4688
rs368420084	in-del	-/GC			intron-variant	NCF2	GRCh38.p7	1:183566715	ATGGGACCTACAGAT[-/GC]CTCCAACTTAGCACA	4688
rs368441566	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183583167	AAGCTATTCTCCTGC[A/C]TCAGCGTCCCAAGTA	4688
rs368553359	snp	A/C/G	0.00557734	0.0525397	intron-variant	NCF2	GRCh38.p7	1:183578216	CTGCCCACTGCCTTC[A/C/G]CCCATGGCTTCTTTT	4688
rs368591589	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567994	AGGCTGGTGTTCAGG[C/T]TTCAGGCTTCCCTCC	4688
rs368718852	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183556818	ATAGGGGTGAGCCAC[C/T]GTGCCTGGCCCAATT	4688
rs368741213	snp	A/C	3.29843e-05	0.00406092	intron-variant	NCF2	GRCh38.p7	1:183566874	CCTCCAGGGAGAGAT[A/C]CCTAAAGGGTGAGAG	4688
rs368781381	snp	G/T	1.64738e-05	0.00286995	missense	NCF2	GRCh38.p7	1:183590227	AAATCCGGGAGTGGG[G/T]GTCCTGGACGGCACT	4688
rs368797395	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183585106	ACATCTTTAAGGTCC[C/T]TTGAGCATCTTGTGG	4688
rs368803722	snp	C/G/T	0.000362348	0.0134555	intron-variant	NCF2	GRCh38.p7	1:183573142	TTGCTCCACATGGCC[C/G/T]GGGCCACAGGAGACT	4688
rs368878005	in-del	-/TTG	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183558209	TTAATTGCTACACAC[-/TTG]TTGTATACTCTCTCT	4688
rs368880633	snp	A/C	0.000153988	0.00877328	missense	NCF2	GRCh38.p7	1:183590307	CCTTCATTCCAGAGG[A/C]TGATGGCCTCCACCA	4688
rs369006606	snp	C/T	6.59087e-05	0.00574021	missense	NCF2	GRCh38.p7	1:183556156	CCAAATCTGTAGTTG[C/T]GCAGTCTTCAACAAA	4688
rs369027769	snp	C/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183558600	AGACAGAGTCTCGCT[C/G]TGTCACCCAGGCTGG	4688
rs369082784	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183579452	AATAATAAGGCCGGG[C/T]GCAGTGGCTCACGCC	4688
rs369123188	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183575146	AGCACCAGCAGAACC[C/T]GGCCCAGACCATGTG	4688
rs369158396	snp	A/G	0.000153988	0.00877328	intron-variant	NCF2	GRCh38.p7	1:183570742	TCACAGAAAGCTCTC[A/G]AGACCTAGGTCCATG	4688
rs369205421	snp	C/T			missense	NCF2	GRCh38.p7	1:183563485	TTAGACACCATGTCC[C/T]GGACCTGGCTGTAGG	4688
rs369293269	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183580310	TTCCACGCATCTTTC[C/T]GGGTTCCTGGAAAGA	4688
rs369332876	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183568185	TTTTTTTTTTTGAGA[C/T]GGAATCTTGGTCTGT	4688
rs369360884	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183584052	AGAAATATTTAAGAG[A/G]TCAACCTGATGAGGT	4688
rs369515038	snp	A/G	4.94205e-05	0.0049707	missense	NCF2	GRCh38.p7	1:183565727	AGCTGGGGTCTTCCA[A/G]GGGCTTTGGAACTAG	4688
rs369678217	snp	A/C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585440	ACCAGCGTGGCCAAC[A/C/G]TGGTGAAACCCTGTC	4688
rs369737178	snp	A/C	8.24205e-05	0.00641899	intron-variant	NCF2	GRCh38.p7	1:183574662	AAACTTGAGACTACT[A/C]CAAATCAAGGTGCCA	4688
rs369794390	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183587640	ATCCAATGATACAAA[A/T]AAAGACAAAGTGGAC	4688
rs369845453	snp	A/G/T	4.94173e-05	0.00497053	synonymous-codon, intron-variant	NCF2	GRCh38.p7	1:183574511	CTCCATCGCCTTGTC[A/G/T]ATTTTGGAATGTCTG	4688
rs369920638	snp	A/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183564650	ATTCCAGTCCTAAAA[A/T]ATCAGAGCCAGTAGC	4688
rs370048375	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183581302	AAAAAAAAAAAGAAA[A/G]AAAGAAAGAAAGAAA	4688
rs370075659	snp	A/G	4.98981e-05	0.00499465	intron-variant	NCF2	GRCh38.p7	1:183567390	CCATCCCCTCACATG[A/G]TGCCATGGCGCAAAT	4688
rs370121318	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183567718	TGTGGTCAGGGGAAC[A/G]GCACAAAGCAGAAGT	4688
rs370123014	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183581858	GTTTTTAGTAGAGCC[A/G]GGGTTTCACCGTGTT	4688
rs370204795	snp	A/G	0.000115332	0.00759293	intron-variant	NCF2	GRCh38.p7	1:183560289	CTGAAATAATAAAGG[A/G]CCTGTTAATTTTCCC	4688
rs370231142	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183570546	ACCGGCATTTGTGGG[A/G]AAGCAGGAGAGTTAG	4688
rs370251291	snp	C/T	0.000153988	0.00877328	missense	NCF2	GRCh38.p7	1:183563295	AGCTCATTGCTGTCC[C/T]GAGGCCGATAGCTGG	4688
rs370318334	snp	A/G	0.00597247	0.0543191	intron-variant	NCF2	GRCh38.p7	1:183562385	TCCAAGAGACCCCTT[A/G]CACTCACACTCACTC	4688
rs370389123	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566012	AGAAGAATCCTAACC[C/T]GCTAAAACGCCCTTG	4688
rs370425896	snp	A/G	3.29962e-05	0.00406165	intron-variant	NCF2	GRCh38.p7	1:183573341	GAAAATGGGGGTGAC[A/G]ATGCTTGTCCTGCCT	4688
rs370670662	snp	C/T	1.66941e-05	0.00288908	intron-variant	NCF2	GRCh38.p7	1:183577754	TAGTGGATGGAGAAA[C/T]AAATGCAGCATAAAA	4688
rs370695184	snp	C/T	1.64909e-05	0.00287144	intron-variant	NCF2	GRCh38.p7	1:183566875	CTCCAGGGAGAGATC[C/T]CTAAAGGGTGAGAGG	4688
rs370795833	snp	A/G	1.65051e-05	0.00287267	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556111	GCTTTGTAGTTTGTG[A/G]AACATCCTAGACTTC	4688
rs370919743	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587733	AAGCATTTTCCCAAA[A/G]GAGCTCATCATTTTA	4688
rs370942685	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183572021	ATATTTGGAGGGCTT[C/T]CACTCACCCAGGCTT	4688
rs370952848	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183580903	AGAATCACTTGAACC[C/T]AGGAGGTGGAGGTTG	4688
rs370991138	snp	A/C	3.34163e-05	0.00408742	intron-variant	NCF2	GRCh38.p7	1:183565830	TTCAAAGTTCCCAGG[A/C]AGGGGTGGATGTGGG	4688
rs371371441	snp	G/T	0.000153988	0.00877328	intron-variant	NCF2	GRCh38.p7	1:183563591	GCTTCACTTCCTGAG[G/T]GGGGAGGAAACAAAG	4688
rs371384794	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183559561	CTCCTCTTTAATAAT[A/C]AAGATGTTTATCGCC	4688
rs371493437	snp	A/G	0.000153988	0.00877328	synonymous-codon	NCF2	GRCh38.p7	1:183567252	ATTGCCCTTCTTCAA[A/G]ACAAAGACAATGTTC	4688
rs371497995	in-del	-/T	0.00953873	0.0683987	intron-variant	NCF2	GRCh38.p7	1:183561696	TGTTGGCCAGGCTGG[-/T]CTTAAACTCCTGACC	4688
rs371503781	snp	G/T	4.94181e-05	0.00497057	missense	NCF2	GRCh38.p7	1:183563298	TCATTGCTGTCCCGA[G/T]GCCGATAGCTGGGTG	4688
rs371563461	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568746	AGCCAGTGCGAAACC[A/G]ATCTCCAACCTGAGG	4688
rs371755664	snp	A/G	0.000249167	0.0111589	intron-variant	NCF2	GRCh38.p7	1:183577747	AGCAGTCTAGTGGAT[A/G]GAGAAATAAATGCAG	4688
rs371775954	snp	C/T	0.000153988	0.00877328	intron-variant	NCF2	GRCh38.p7	1:183574445	GAGACAAATGAGAAT[C/T]CAGTGACATCCTCTC	4688
rs371817117	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572305	TTCTCCTGCCTCAGC[C/T]TCCCAGGTAGCTGGG	4688
rs371840639	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183563685	CACAGGGGGTACCCA[A/G]TACAGCAGGGGAGAG	4688
rs371974153	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183561326	TTTATTGAGAGGCAA[C/T]ACAATGAGGTGGAAA	4688
rs372137411	snp	C/T	3.29571e-05	0.00405924	intron-variant	NCF2	GRCh38.p7	1:183566912	GTCAGGCCTTGGCAT[C/T]ACATTACCTGGGGCT	4688
rs372240997	snp	C/T	0	0	intron-variant	NCF2	GRCh38.p7	1:183566020	CCTAACCCGCTAAAA[C/T]GCCCTTGCCGCTTTA	4688
rs372270951	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587367	GGGAGGCCAAGGCAG[A/G]TGGATCACTTGAGCC	4688
rs372513540	snp	A/G	0.00056015	0.0167261	intron-variant	NCF2	GRCh38.p7	1:183574639	AGAAAAGTACAGACC[A/G]CAACATAAAACTTGA	4688
rs372513979	snp	A/G/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183568138	TCATCCAGCCCCCTC[A/G/T]TTTTTGTAGTTGCTT	4688
rs372619316	snp	A/G	4.94189e-05	0.00497062	intron-variant	NCF2	GRCh38.p7	1:183573136	CCCACCTTGCTCCAC[A/G]TGGCCCGGGCCACAG	4688
rs372629769	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564695	TCACAAAATCATCCT[A/G]GGTTTATATGTGATC	4688
rs372630984	snp	A/G	0.000461163	0.0151779	intron-variant	NCF2	GRCh38.p7	1:183586990	GGCCTGAGGAGAGAA[A/G]GGTCCAGACATGGCC	4688
rs372773130	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183574500	ACCCAGACACACTCC[A/G]TCGCCTTGTCGATTT	4688
rs373013877	in-del	-/AAGT			downstream-variant-500B	NCF2	GRCh38.p7	1:183555259	TAGTCTTGTGTAAGT[-/AAGT]GCACTCTAGATGAGT	4688
rs373014973	snp	A/G	1.6489e-05	0.00287128	intron-variant	NCF2	GRCh38.p7	1:183560324	TCCTGCCAAGTGAAC[A/G]CTGAACATCACTAAA	4688
rs373072570	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183565558	GGTGCAGGAAAGGGG[A/G]ATTCTGGGGCTGCGT	4688
rs373201877	in-del	-/GAT			intron-variant	NCF2	GRCh38.p7	1:183556479	AAAAAGTTACCAGAT[-/GAT]AGAGAAGAAGGGTCA	4688
rs373224226	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183558129	TCCACTCACCTTGGC[C/T]TCCCAAAGTGCTGGG	4688
rs373262281	in-del	-/G	0.000165155	0.00908573	intron-variant	NCF2	GRCh38.p7	1:183567184	ATGCCCATCGCACCA[-/G]CCCCTGATCCTCTGC	4688
rs373312840	in-del	-/ATGGTCCTTTGC			intron-variant	NCF2	GRCh38.p7	1:183577355	GGGGCTCATTTTTGC[-/ATGGTCCTTTGC]GCTTCACATTAATAA	4688
rs373387380	snp	G/T	1.66263e-05	0.00288321	intron-variant	NCF2	GRCh38.p7	1:183570757	GAGACCTAGGTCCAT[G/T]GAGAAGGTCAGGACT	4688
rs373508925	snp	A/T	8.23744e-05	0.0064172	intron-variant	NCF2	GRCh38.p7	1:183577596	AGGCCCTGTTCTCCT[A/T]ACCTCACAGGCAAAC	4688
rs373617506	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183581319	AAGAAAGAAAGAAAA[A/G]AAAGTCCAACAACCA	4688
rs373646186	in-del	-/TGAAAGTCTTGGAAAGCCAA			intron-variant	NCF2	GRCh38.p7	1:183589750	CAAAGTCGACACACA[-/TGAAAGTCTTGGAAAGCCAA]AAGAGGTGCCTTAGA	4688
rs373651328	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183571178	ACTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC	4688
rs373768930	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183576042	GGTTCTCAGCCACCT[C/T]CTCTTAAGACATTTC	4688
rs373824651	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183562705	GGGTGCAGTGGCAGG[G/T]GCCTGTAATCCCAGC	4688
rs373876135	snp	A/G	1.64754e-05	0.00287009	missense	NCF2	GRCh38.p7	1:183563212	CTGTGTTCTCACACC[A/G]CAGAGTCAGGCAGTA	4688
rs374088218	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580966	CCTGGTTGACAGAGC[A/G]AGACTCCAACTCAAA	4688
rs374127238	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183559697	AACCCCATCTCTACT[A/G]AATACACAAAAATTA	4688
rs374145879	snp	C/T	0.000230593	0.0107351	intron-variant	NCF2	GRCh38.p7	1:183569103	TCAGCTCAGGCTTGG[C/T]GCTTGGATATTCTAT	4688
rs374166487	snp	C/T	6.59044e-05	0.00574002	intron-variant	NCF2	GRCh38.p7	1:183573308	CTGTAACACAGAAAA[C/T]GTAGCATTCCCTTAT	4688
rs374177506	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183568214	GTTGCCCAGGCTGGA[C/G]TGCAGTGACATGATC	4688
rs374248950	snp	A/G	4.94858e-05	0.00497398	intron-variant	NCF2	GRCh38.p7	1:183565798	AAGGCAACAGGGAGC[A/G]ACGGTCAGAACCTTC	4688
rs374268796	snp	C/T	1.64879e-05	0.00287118	intron-variant	NCF2	GRCh38.p7	1:183577570	AGCCATGATCCCCTC[C/T]TGCCCAGGCCAGGCC	4688
rs374311583	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574824	TTAAGAAAACACCAT[A/G]GAATGCGTAAATGCA	4688
rs374401679	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183585035	TGTGTCTGTGGTTTT[C/T]CTTTTAGAAAAGACT	4688
rs374402066	snp	A/G	9.88452e-05	0.00702942	stop-gained	NCF2	GRCh38.p7	1:183577661	TCAGCTGGTTCCCTC[A/G]AAGCTGAATCAAGGC	4688
rs374533854	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183571973	TGTTGCATGGATATA[C/T]CACATTTTGATTACT	4688
rs374580539	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183580943	AAAACCATGCCACTG[C/T]ACTCCAGCCTGGTTG	4688
rs374667798	snp	C/T	1.64798e-05	0.00287047	missense	NCF2	GRCh38.p7	1:183556137	ACTTCTCTCCGAGTG[C/T]TTTCCAAATCTGTAG	4688
rs374675149	in-del	-/AA			intron-variant	NCF2	GRCh38.p7	1:183587595	AAGGCACCCTGTCTC[-/AA]AAAAAAAAAAAAAAA	4688
rs374749443	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183577320	CACACTCGTGTCCAG[C/T]CTCCCTTCAGAGAGC	4688
rs374804194	snp	A/G	3.30573e-05	0.00406541	intron-variant	NCF2	GRCh38.p7	1:183563597	CTTCCTGAGTGGGGA[A/G]GAAACAAAGGGAACT	4688
rs374822007	snp	C/T	1.65141e-05	0.00287346	intron-variant	NCF2	GRCh38.p7	1:183567160	GACTGCATTTGCTGC[C/T]AGGATCCCATGCCCA	4688
rs374900622	snp	C/T	1.64787e-05	0.00287038	intron-variant	NCF2	GRCh38.p7	1:183563387	CCTCCTCCAGGCCAG[C/T]ACAAGGTTCCCACTG	4688
rs374994150	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183574864	GTACTCTTCCAACAA[C/T]GAAATAGGTCAGGAA	4688
rs375036440	snp	C/G	8.23621e-05	0.00641672	intron-variant	NCF2	GRCh38.p7	1:183574466	ACATCCTCTCAACAC[C/G]TGCATCACCAATACG	4688
rs375147692	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183566518	AAAGTGCTAGGATTA[-/C]CAGCCATGAGCAACT	4688
rs375291905	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183558592	TTTTTTTAAGACAGA[A/G]TCTCGCTCTGTCACC	4688
rs375338665	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183583719	TCAAAAGAGGGAGCA[C/G]ACGCTGCCTTAGTGG	4688
rs375362872	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183572288	CACCCGGATTCAAGC[A/G]ATTCTCCTGCCTCAG	4688
rs375599151	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183565328	TTTCCAGATACAGTG[A/C]CTCAGACATTTGAAA	4688
rs375646530	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183558634	GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT	4688
rs375696114	in-del	-/GAGT			downstream-variant-500B	NCF2	GRCh38.p7	1:183555434	TATTCAGTATTGAGT[-/GAGT]TCTTAACACATGTTC	4688
rs375701671	snp	C/G	1.64841e-05	0.00287085	intron-variant	NCF2	GRCh38.p7	1:183574657	ACATAAAACTTGAGA[C/G]TACTCCAAATCAAGG	4688
rs375774362	snp	A/G			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555651	GCCAATTACAGTAAT[A/G]GTTCAGAAACAGGAA	4688
rs375817556	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183567599	CACTAGATAGTGAGG[A/T]CTTACAATCCTTGCC	4688
rs375864205	snp	A/C	8.23662e-05	0.00641688	intron-variant	NCF2	GRCh38.p7	1:183563955	TGTGGTTGATAGCCC[A/C]AGCTATCCCATCTTC	4688
rs375927031	snp	C/T	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183570533	TAGAGATGTGAAGAC[C/T]GGCATTTGTGGGGAA	4688
rs376021881	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575350	TGGCAGGCACCTGTA[A/G]TCTCAGCTACTTGGA	4688
rs376075687	snp	C/T	0.000153988	0.00877328	intron-variant	NCF2	GRCh38.p7	1:183570771	TGGAGAAGGTCAGGA[C/T]TGCCTTACCTGTGGT	4688
rs376187258	in-del	-/G			intron-variant	NCF2	GRCh38.p7	1:183582700	TTTCCAAGTCAGCAG[-/G]AAGAAGGCTTTGCTA	4688
rs376461528	snp	C/T			upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590710	ACCCCTGTTCTGTGG[C/T]AGCTTCTGGCCAAAG	4688
rs376657753	snp	G/T			intron-variant	NCF2	GRCh38.p7	1:183581346	ACCAAAAAAACAGGG[G/T]GGGGCCAGGGGCTGA	4688
rs376681445	in-del	-/AAAC	0.0162398	0.0886349	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555572	CATAATGAAAAAAGA[-/AAAC]AAACAAGTTTATTTG	4688
rs376705802	snp	C/T	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183574076	GGCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA	4688
rs376920441	snp	C/T	0.000153988	0.00877328	missense	NCF2	GRCh38.p7	1:183556168	TTGCGCAGTCTTCAA[C/T]AAAAACTTTGGGGAA	4688
rs376994104	snp	A/G	4.94173e-05	0.00497053	missense, intron-variant	NCF2	GRCh38.p7	1:183574503	CAGACACACTCCATC[A/G]CCTTGTCGATTTTGG	4688
rs377018812	snp	C/G	0.000153988	0.00877328	intron-variant	NCF2	GRCh38.p7	1:183564062	GGGAGTAAAACAAAA[C/G]AAGATGGTGAATGAA	4688
rs377089938	snp	C/T	8.23621e-05	0.00641672	intron-variant	NCF2	GRCh38.p7	1:183569213	CAGGAGAAGTGAAAA[C/T]GGAAAAGGCAATGAG	4688
rs377173180	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183573650	TCATGACAGTGCTCC[C/T]TTGGATGGGTGTTTG	4688
rs377173805	snp	A/C/G	3.32012e-05	0.00407427	intron-variant	NCF2	GRCh38.p7	1:183577744	TACAGCAGTCTAGTG[A/C/G]ATGGAGAAATAAATG	4688
rs377217293	snp	A/G	0.000264367	0.0114941	intron-variant	NCF2	GRCh38.p7	1:183567358	GCCCTGCAGAGGATA[A/G]ACACAAGATCCAGCC	4688
rs377274027	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588722	AAATGCTAGTAGGAA[A/G]GGCTCAAGCAGGAAA	4688
rs377362786	snp	G/T	0.000708641	0.0188101	intron-variant	NCF2	GRCh38.p7	1:183573334	CTTATGTGAAAATGG[G/T]GGTGACGATGCTTGT	4688
rs377469880	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575901	GGAAGTGGAAATCTG[A/G]ACTCCTTTCAGTCCT	4688
rs377522028	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183571321	CAGGTTTTCACCATG[C/T]TGGCCAGGCTGGTCT	4688
rs377591562	snp	A/C	4.94214e-05	0.00497074	missense	NCF2	GRCh38.p7	1:183563243	GTTTTTCACCTGGCC[A/C]CAGGCATCCTTCATG	4688
rs377686504	snp	A/G	0.00993419	0.0697739	intron-variant	NCF2	GRCh38.p7	1:183559732	GGCATGGTGGTGGGC[A/G]CCTGTAATCCTAGCT	4688
rs377710686	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558970	GTGCACAGACTCAGC[A/G]TATGAGCAGGGCTTT	4688
rs386637448	multinucleotide-polymorphism	AGC/TGT			intron-variant	NCF2	GRCh38.p7	1:183582230	CTCTAGCCCTTCTTC[AGC/TGT]GGTTCTCTTCGTGGC	4688
rs386637449	in-del	ATA/CT			intron-variant	NCF2	GRCh38.p7	1:183584915	TTAAAAAAAGAATTT[ATA/CT]AAGTCACAATAAATA	4688
rs386637450	multinucleotide-polymorphism	AG/GA			intron-variant	NCF2	GRCh38.p7	1:183589302	GGTGTGAAGTTCCAC[AG/GA]GACATTAATAGTTTG	4688
rs386637451	multinucleotide-polymorphism	CC/TG			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592382	TGCTAAATCTAGCCC[CC/TG]AACTCTGGGTAGTAG	4688
rs386637452	multinucleotide-polymorphism	AACCA/TAATT			upstream-variant-2KB	NCF2	GRCh38.p7	1:183592693	AATTATTCCTGAGAA[AACCA/TAATT]AATGGATTTGTAGCT	4688
rs397701737	in-del	-/TT			intron-variant	NCF2	GRCh38.p7	1:183578365	CCTCCTTTTTTTTTT[-/TT]CTTTTTTTTTGAGAC	4688
rs397951870	in-del	-/ATG			utr-variant-3-prime	NCF2	GRCh38.p7	1:183555719	TGTTTTTGTAAGATG[-/ATG]CTAGGTTTTTTTTTA	4688
rs397982208	in-del	-/A	0	0	intron-variant	NCF2	GRCh38.p7	1:183571134	CGTGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	4688
rs397982209	in-del	-/T	0	0	intron-variant	NCF2	GRCh38.p7	1:183579764	GCTGTTATTATTCTC[-/T]TTTTTTTTTTTTTTT	4688
rs397982210	in-del	-/A	0	0	intron-variant	NCF2	GRCh38.p7	1:183581686	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAACACT	4688
rs527247519	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565202	GCTTCAAGTGCACTT[C/G]CCAAGACAGCCCTCT	4688
rs527373547	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558231	ATACTCTCTCTACCC[C/T]CATTAACTTTTTTTT	4688
rs527432152	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183587094	CTGCTGTCTGCCCTC[A/G]TCGGCACCTCGAGGC	4688
rs527662890	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591779	CAGGAGTGAGCCACC[A/G]TGCCCAGCCGAAATA	4688
rs527782266	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183588591	TTTAAATAAATAATA[A/G]AATTTATTGCAAATG	4688
rs527835292	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592399	AACTCTGGGTAGTAG[G/T]AGAATTTTCCTCTCC	4688
rs527851856	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586525	CTGGGATGAAGCCAG[A/G]TTTTGATGCAGTTTC	4688
rs527855046	snp	A/C	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183578563	TAGAGACCAGGTTTC[A/C]CCATGTTGGCCAGGC	4688
rs528009583	snp	A/G	0.00755907	0.0610114	intron-variant	NCF2	GRCh38.p7	1:183581746	CGATCTCGGCTCACT[A/G]GAAGCTCCGCCTCCC	4688
rs528011813	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579464	GGGCGCAGTGGCTCA[C/T]GCCTGAAATCCCAGC	4688
rs528107961	snp	A/G	0.0023933	0.0345097	intron-variant	NCF2	GRCh38.p7	1:183583763	GGGCAAAGGCACGGA[A/G]GATGCATGAGTGGGT	4688
rs528239550	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	NCF2	GRCh38.p7	1:183563273	GCTGTCTTCTGAAAG[A/G]GGCACCAGCTCATTG	4688
rs528277062	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183570117	CCTGCTCAGAAAACC[A/G]CCCTCTGCTAGTGCT	4688
rs528361273	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555798	TTTACAGTGTGAACA[C/T]AGCTGGCTAGCTAGC	4688
rs528463024	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568528	TCATCACTTTGAGAG[A/G]ATTCTTAAGAAAGCT	4688
rs528481761	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575885	GGCCAGGATCAACCC[C/T]GGAAGTGGAAATCTG	4688
rs528588181	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183561975	AATTTTTGTATTTTC[A/G]GTAGAGATGGGGTTT	4688
rs528707670	snp	C/T			upstream-variant-2KB	NCF2	GRCh38.p7	1:183591200	AGGTAGTGTGGCCCA[C/T]TGAGGCCTGGGCAGG	4688
rs528730616	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183575287	TCAGCCTGGCCAACA[A/T]GGAGAAACCCTGTCT	4688
rs528747111	snp	C/T	4.07839e-05	0.00451556	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590423	GCTGCCTTAGTGGCC[C/T]CCAAGGTGTTCACTT	4688
rs528757061	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580158	TAGCAGTGGCTATGC[A/G]GGAAATAAAAGAAGA	4688
rs528788918	in-del	-/AAAGT	6.60186e-05	0.00574499	intron-variant	NCF2	GRCh38.p7	1:183556242	TCACTGATAAAAGGA[-/AAAGT]AAAGTACACATGGAT	4688
rs528816712	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577127	TACATGGGGTAAGAA[C/T]CATGGATAGTAAAGA	4688
rs528839763	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183558869	AGGCCCAGCCTACCC[A/T]CATTAACTTTAAAAT	4688
rs528899248	in-del	-/AGAT			intron-variant	NCF2	GRCh38.p7	1:183556476	TTTCAAAAAGTTACC[-/AGAT]AGAGAAGAAGGGTCA	4688
rs528926369	snp	A/C	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183587740	TTCCCAAAGGAGCTC[A/C]TCATTTTAAAAATGG	4688
rs528967028	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183585582	GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC	4688
rs529030440	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183589579	TGCGAGACATCCCAC[A/G]CCATGCCCCCAGCAG	4688
rs529049509	snp	A/T			intron-variant	NCF2	GRCh38.p7	1:183579990	ATTATCAGGATATTT[A/T]AAAAATACATGGCAT	4688
rs529061828	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581760	TGGAAGCTCCGCCTC[C/T]CGGTTCACGCCATTC	4688
rs529069044	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183588808	CAGAGACATGTGGGC[C/T]TGAAGGCCTGGGAGC	4688
rs529212845	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582462	CACAAGCTCCAGGCT[C/T]GAGAGAGTTTATAAT	4688
rs529310799	in-del	-/A	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183568681	AAAGGACGTCATTCT[-/A]GATTCCTGACTCCAG	4688
rs529426144	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580383	TTCTAAGCCAGAAGG[G/T]GGGGTAACTAGCTTC	4688
rs529429624	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574109	CAAAACAAAACATTT[C/T]TGCTGAGAGCTGTTA	4688
rs529470393	snp	G/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183581148	TTAGCCAGGCATAGT[G/T]GTACGTGCCTGTAGT	4688
rs529496026	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573571	CTCTGTGTGCTGTCC[G/T]TGGGGTTCTCTCATG	4688
rs529676655	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571792	AGCAGACATGGTCTC[A/T]GCTCTCTCAGTGCTT	4688
rs529770418	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183577501	AAATGGCTTTTCCAA[A/G]CTCCTGGAGGTGTCA	4688
rs529805060	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565114	CTGATGATCAGGCGC[A/G]TGTGGCAATCATTGA	4688
rs529843093	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564275	TAGGTAATTACCAAA[A/G]GACCAGCATATCCTC	4688
rs530584489	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183577193	TGGCAGGTCCTGCAC[A/G]GACAATGAACTCATG	4688
rs530584547	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569270	GCTAATGGTAATTTG[A/G]GCATTCTTCCAGACC	4688
rs530621065	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576533	CGATGCGCAGGACGC[A/G]CCACAACCCCTCTCT	4688
rs530643019	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183581692	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTT	4688
rs530696845	snp	C/G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183571015	CAGCAACTGAAGAAA[C/G/T]GAGCATTCACCCCAC	4688
rs530704541	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563127	ACAGAAGGTGCTTGA[A/T]AAATTTCAAATTGTT	4688
rs530735929	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183584348	ACACCTAGGGAATTG[C/T]GCAAGAGGGCCTGCT	4688
rs531023940	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568452	GATTTCAGGCATGAG[A/C]CACACACCTGGCCAA	4688
rs531033509	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560349	ACTAAAGGAAACAGC[A/G]AAATGTCAAAGTAGA	4688
rs531062648	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567890	AGGCTGCCCAGCTGC[C/T]GTGGTGCAGTGTCGG	4688
rs531062684	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575815	ACTTGCCAAACTCAG[A/G]CAGGTGGAAGGATTG	4688
rs531170931	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566713	CAATGGGACCTACAG[A/G]TGCCTCCAACTTAGC	4688
rs531187446	snp	A/C			intron-variant	NCF2	GRCh38.p7	1:183574973	AGTTGCTTTAGTAAA[A/C]GAGTGACTTGCTCAA	4688
rs531296807	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183558327	GGCTGGAGTGCAGTG[A/G]CACAATCTCAGCTCA	4688
rs531412962	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584585	TGGAGGAAATTCTTT[C/T]TGGGAGCCTTCACTC	4688
rs531628068	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592498	ATGGGCTCCTTGGAA[A/G]TTGGGACCATGCCTT	4688
rs531662382	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183564337	GGTCAATTAAGCCCA[C/T]GGGATCCAAAGCAAT	4688
rs531672469	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183581261	CACTCCAGCCTGGAC[A/G]ACAGAATGAAATCCT	4688
rs531762505	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572721	CATAGCTCACTGTAG[C/T]CTTGAACTCCTGGGC	4688
rs531881293	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183586550	AGTTTCATGATCATC[C/T]CCATTCTGTGACAGC	4688
rs532107179	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563652	AACATCCTGGATCAC[C/T]GCAGTTTCGTGATTT	4688
rs532135800	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556002	TTTAACAGGGAATAA[A/G]TAGTTAACACTTCCA	4688
rs532294062	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183556622	CTGCAACCTCTGCCT[C/T]CTGGGCTCAAGTAAT	4688
rs532362215	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183562207	CAGCCACCAAATAGA[C/T]TGAAGCTGCTGTCAA	4688
rs532527525	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183587753	TCATCATTTTAAAAA[C/T]GGACTTGACAATATG	4688
rs532549013	in-del	-/C			intron-variant	NCF2	GRCh38.p7	1:183568905	AGCCCTGATGGCCAG[-/C]CCCACCACAGTCAAG	4688
rs532579007	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591015	TACTACCTATGTCCT[G/T]CCCCTCCCCTATTCT	4688
rs532901316	snp	C/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183584559	AGATCCTGGGACTCA[C/T]GGGCATTTTTTGGAG	4688
rs532919390	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571838	TATTTCCTATAAACG[A/G]AATTGTACAACATGT	4688
rs533030111	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183559409	TAAGGCAAAATTTAC[C/T]TACTTTTCTCTTTGA	4688
rs533070652	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569244	GGAAAGCAGGGGAGA[C/G]ACAACAAACGGCTAA	4688
rs533278871	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183588257	AGAGTAGTAATTACT[A/G]TTTATTGCTCTGTGG	4688
rs533289726	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568715	GCTCTGGCCTGCCCC[C/T]GTCAGAGGGGACTGC	4688
rs533307200	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559399	AGCTGGTTTTTAAGG[C/T]AAAATTTACCTACTT	4688
rs533434483	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183558166	AGCATGAGCCACCAC[A/G]CCCAGCCTATACTAC	4688
rs533448375	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183564542	TATTTACTATAGGGG[A/G]TACATGATCAGAGAA	4688
rs533465609	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560282	GGTCACCCTGAAATA[A/G]TAAAGGGCCTGTTAA	4688
rs533500800	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant	NCF2	GRCh38.p7	1:183574531	TGGAATGTCTGGGCT[C/T]AGACTTCATGCTCGT	4688
rs533510036	in-del	-/A	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183566504	TCACCTCAGCCTTCC[-/A]AAGTGCTAGGATTAC	4688
rs533611950	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580258	ACTAAATGCATGCAG[A/G]CCATTCTTTAAGTAG	4688
rs533843234	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592596	AAATCATTGGTAAAT[G/T]ACCTGCAGGTAGCAG	4688
rs533855148	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183587739	TTTCCCAAAGGAGCT[C/T]ATCATTTTAAAAATG	4688
rs533957935	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183579123	AGGCTGGCAGGAATC[C/T]TCAAGAGGCAGTGTG	4688
rs533997069	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586274	GGGAGGCGGAGGCTG[C/T]GGTGAGCTGAGATCG	4688
rs534011480	snp	C/G			missense	NCF2	GRCh38.p7	1:183560248	TTTTCACTTTCCTTG[C/G]GTTCATCTGGAAAGC	4688
rs534281662	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183557484	CCATTTAGGAAGATT[C/T]GCAGGTGATTCACAT	4688
rs534293121	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568888	CCACGTAGCTGCAGC[A/C]AAGCCCTGATGGCCA	4688
rs534330412	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183576168	AGGAAGAGAAGGATT[A/G]TAAGTAGGGAAATGA	4688
rs534374716	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183571264	CTGATATTACAGGCA[C/T]CCGCCACTGTGCCCG	4688
rs534444949	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561569	ATTTAGACTTGGTTA[A/G]TGGTAAGTGTTCCTG	4688
rs534490747	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564391	CAGAGGCCACAGGAA[A/G]AAGTATTAGAACCAC	4688
rs534490818	snp	A/C	6.59141e-05	0.00574045	missense	NCF2	GRCh38.p7	1:183556145	CCGAGTGCTTTCCAA[A/C]TCTGTAGTTGCGCAG	4688
rs534983535	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560413	GTGCCTTGTGTAGAG[C/T]TTATATGCTCTTTAT	4688
rs535023017	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559613	CCTGTAATCTCAGTA[A/C]TTTAGGAGGCCGAGG	4688
rs535255362	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589146	CTGTCTTCCTGTCAG[G/T]AGGGTGTGGCTGAGG	4688
rs535272710	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574821	GTGTTAAGAAAACAC[C/T]ATGGAATGCGTAAAT	4688
rs535305485	snp	A/G	0.0103295	0.0711199	intron-variant	NCF2	GRCh38.p7	1:183581347	CCAAAAAAACAGGGT[A/G]GGGCCAGGGGCTGAG	4688
rs535437538	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572233	CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCATG	4688
rs535486562	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183580751	GGAGGCCAAGGCAGG[C/T]GGATCACTTGAGGTC	4688
rs535561432	snp	C/T	0.00315893	0.0396167	synonymous-codon	NCF2	GRCh38.p7	1:183566926	TCACATTACCTGGGG[C/T]TGCTGCTGAGGGTGG	4688
rs535597291	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572856	GGCATGAGCTACCCT[G/T]CCTGGCCCTCTCTTC	4688
rs535658703	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565489	CACCCAAGCCCCGTG[A/G]GTGTTCTGCAGAAGG	4688
rs535758757	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183584794	ACAGGCAGTTAGAGG[C/T]AAGACGTCGGTCAAG	4688
rs535790330	in-del	-/TTTG	0.0138799	0.0821421	intron-variant	NCF2	GRCh38.p7	1:183558266	TTTAATTTTTTTGTT[-/TTTG]TTTTTGTTTTTTTTT	4688
rs535799780	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183558469	GACAGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT	4688
rs535838441	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555228	GGTAACCTAGCTGTG[A/T]AGTAGGCTATACCAT	4688
rs535856451	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578839	TGGACACACACTTCT[C/G]AGGATGCTGGCCCAG	4688
rs536219722	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563741	AGCCTAAAAGGCCTT[C/T]AGAGGTCCTTTAGCC	4688
rs536272781	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589989	TTTTAAAACTGGCTG[C/T]CTGGGGCCCCTCCCA	4688
rs536297700	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591058	GCCCCAGACTCACCC[A/G]CACTGGGGGGACTTT	4688
rs536300413	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183583879	ATTGCTTTTTTTAAA[C/T]TTTTTTTTATTTTAC	4688
rs536372426	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183575635	TATTATGGAAATTAG[A/G]GGGTGTGACATTTGA	4688
rs536373941	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NCF2	GRCh38.p7	1:183556060	GCAGAAGGGTGCTAA[A/G]TCTTACAAACAAGTA	4688
rs536464474	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576932	GTGGGAAGGGCCAAC[C/T]GGAAAAAGTAAATGA	4688
rs536566647	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183565199	TCTGCTTCAAGTGCA[C/T]TTCCCAAGACAGCCC	4688
rs536808623	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183561376	GAGAAAGGTTTGTAT[C/G]CCACCTCCACTGCTT	4688
rs536830799	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577511	TCCAAGCTCCTGGAG[G/T]TGTCAACAGATCACT	4688
rs536870357	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183584667	GACCTTAGAGTTTGC[A/G]TTTTGAGATTTAAGA	4688
rs537031179	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183582730	ATGGAGCCTCTTTAA[A/G]CCAGCTCCATGGAAT	4688
rs537253657	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560620	AGATCCCTTGCATGC[A/G]CAGTTCACAATAGGG	4688
rs537302019	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589055	CCTCCAGCCAGAGGT[C/G]GGGGGTCCTGCCATG	4688
rs537359841	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571837	ATATTTCCTATAAAC[A/G]GAATTGTACAACATG	4688
rs537417395	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183558658	GCAACCTCCACTCCC[A/G]GGTTCAAGCGATTCT	4688
rs537473125	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592697	ATTCCTGAGAAAACC[A/T]AATGGATTTGTAGCT	4688
rs537628401	in-del	-/GT	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183571546	TGTACCCATTAAGCA[-/GT]GTGTCCACACTCCCC	4688
rs537644887	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183588390	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	4688
rs537660849	snp	A/G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587274	CTGCTTTTGTTAGTC[A/G/T]TATATGGCCTAGAAA	4688
rs537706625	snp	G/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183581678	CCTTGCTAAGTGTTT[G/T]TTTTTTTTGAGACAG	4688
rs537900921	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586775	ACTGTCCCCAGAAGG[A/G]CCAGTCACATTTCCC	4688
rs537996455	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578721	TGCTGGATTGGCGTG[G/T]AGCTGACTGGCTCGA	4688
rs538180809	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183573683	GATGAGGATAGACAT[A/T]TAAAGACTGGCTTGA	4688
rs538231551	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183562662	AGATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4688
rs538254272	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585697	GCACACTGGTGGAAC[A/G]GTTTCTACAAAGGGT	4688
rs538266239	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589026	CCCCTGAGAGGAGGT[A/G]GGGCCATGTCCTTCC	4688
rs538269136	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183557667	AGGTCATAGTAAGAC[A/G]CATACTGGCTTCTCT	4688
rs538345147	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555179	TAGTAACATGCTGTA[C/T]AGGTTTGTAGCCTAG	4688
rs538356851	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183560537	GGTGGGTTGGGGGGT[A/G]GTTTCAGGATAAAAT	4688
rs538407059	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183564549	TATAGGGGGTACATG[A/T]TCAGAGAAGGCCACT	4688
rs538509883	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183584989	GATATCTTCTCCCAA[C/T]CCCAGGCTCTCTTTC	4688
rs538602861	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570298	CTTGGGCAGAAAAAG[G/T]GTTCACTCTCAGTGC	4688
rs538716172	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589909	ACTTGTAGAATGATT[G/T]TAATTTAGAAGATGG	4688
rs538735832	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572082	CTACCCGACCACTGG[G/T]CAACTTTAGCCCTAT	4688
rs538760999	snp	A/G	6.58924e-05	0.0057395	synonymous-codon	NCF2	GRCh38.p7	1:183563303	GCTGTCCCGAGGCCG[A/G]TAGCTGGGTGGGGAT	4688
rs538880599	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591879	GACAGTGAATTATGA[A/C/T]TTCTCCCATCTTCCA	4688
rs538961206	snp	C/G/T			intron-variant	NCF2	GRCh38.p7	1:183561429	AGCAGTGTAACTTCT[C/G/T]AGAACCTCAGTTACC	4688
rs539060806	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183564957	AATAGAATGGAGCAG[C/G]GCGAGTTCATGGTGC	4688
rs539191669	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183581822	ACAGGCGTCCGCCAC[C/T]GCGCCCGGCTAATTT	4688
rs539219349	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583841	TCTTGCAGTCATGGA[A/C]GCCACTGGAAGTTCT	4688
rs539221356	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576244	TCAGCTTTACTTGCA[A/G]AGAGGGCCACTCAGC	4688
rs539231015	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183568020	CCTCCCTTTACTCCC[C/T]ACTCTGTTACTTTCC	4688
rs539242567	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	NCF2	GRCh38.p7	1:183590509	TTGCAAATGCATCAG[A/G]AAATGTCCCCACCTT	4688
rs539258527	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582995	GGAAATAGAGGGGGA[A/G]AAACCTCCATCCATA	4688
rs539261246	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183575354	AGGCACCTGTAATCT[C/T]AGCTACTTGGAGGCT	4688
rs539273435	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183566552	GCTGGCCTCATTTTC[C/T]TTCTAATGGCATTGT	4688
rs539343633	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183571267	ATATTACAGGCACCC[A/G]CCACTGTGCCCGGCT	4688
rs539386607	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183560569	GTTCCACCTCAGATC[A/G]TCAGGCATTAGATTC	4688
rs539568553	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183574857	ATCATTTGTACTCTT[C/T]CAACAACGAAATAGG	4688
rs539572768	snp	A/G	0.00795532	0.062565	intron-variant	NCF2	GRCh38.p7	1:183586211	TGGTGGCGCATGCCT[A/G]TAGTCCCAGCTACTC	4688
rs539577314	snp	G/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183557944	CAAAGGTGCAATCTT[G/T]ACTCACTGCAAGCTC	4688
rs539632630	snp	C/T	1.65018e-05	0.00287239	missense	NCF2	GRCh38.p7	1:183567239	TGGCCCAGTTATCAT[C/T]GCCCTTCTTCAAGAC	4688
rs539703702	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587500	TTGGGGGACTGAGGT[A/G]GGTCAATCGCTCAAG	4688
rs539789892	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183565559	GTGCAGGAAAGGGGG[A/G]TTCTGGGGCTGCGTG	4688
rs539932319	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183589314	CACGAGACATTAATA[A/G]TTTGGCATCTCACTT	4688
rs539934135	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183558377	GGTTCAAGAGATTGT[C/T]CTGCCTCAGCCTCCT	4688
rs540193843	snp	G/T	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183572995	GGAGAAATGGGAGCA[G/T]CTTGGAGAAAATAAA	4688
rs540228231	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183585391	AGTACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	4688
rs540247375	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569238	AATGAGGGAAAGCAG[A/G]GGAGAGACAACAAAC	4688
rs540256235	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183584137	GGAGGCCAGCCATAT[A/G]GGAGAGGGTGGCCTT	4688
rs540288856	snp	C/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183585949	ATCCAGAGAGAATTA[C/T]TGATAACATTTTGAT	4688
rs540457866	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578503	GGACTGAGCTGGGAC[C/T]ACGGGCGAGCGCCAC	4688
rs540593484	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183560697	GCAGAGCTCAGGCCA[A/G]TATACCTGCAGCTCA	4688
rs540603317	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577100	TCAGTCTCTCTTTAG[G/T]TATCAATCAAGTACA	4688
rs540686057	in-del	-/A	0.00199481	0.0315187	intron-variant	NCF2	GRCh38.p7	1:183586342	CTGTCTCGGAAAAAG[-/A]AAAAAAAATTAACAT	4688
rs540765895	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183569653	GAGTGCAGTGGCGCG[A/G]TCTTGGCTCACTGCA	4688
rs540801897	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563376	TCCTCCTCTTCCCTC[C/T]TCCAGGCCAGCACAA	4688
rs540838721	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183562990	CTGCCCTGCTGGGCC[C/T]GCTGTTCTCTTGTGG	4688
rs540858921	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589588	TCCCACACCATGCCC[C/T]CAGCAGACATCACTA	4688
rs540889331	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183583453	GTTACCCACTTCTGC[C/T]TTGCATTACAGTTAC	4688
rs540934675	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183580421	TGAGCCTCTTCCATC[A/G]CGAAGAGGACAGGCA	4688
rs540961313	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NCF2	GRCh38.p7	1:183555285	TGAGTTTGCACAACA[C/T]GTTTCTCAGATCATG	4688
rs541248065	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575207	AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	4688
rs541755573	snp	A/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183575508	GGCTGTGGTTCTTGA[A/G]TGTCTATTTTACTAT	4688
rs541794214	snp	C/T	0	0	intron-variant	NCF2	GRCh38.p7	1:183572579	CTAAAACGTGAACTA[C/T]AAGGAGCATTAATCC	4688
rs541838904	snp	A/C/G	4.94461e-05	0.00497202	synonymous-codon	NCF2	GRCh38.p7	1:183563508	GCTGTAGGGGAGCCC[A/C/G]GGCTGAGTCTTCATG	4688
rs542018613	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592869	GCTTACTCTTCTCCC[A/G]CTATGCCTTCATTCC	4688
rs542024029	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566376	GGCTGGCAAGGCCCA[C/T]TCTGATTCAAAGCTC	4688
rs542053305	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NCF2	GRCh38.p7	1:183592387	AATCTAGCCCTGAAC[G/T]CTGGGTAGTAGGAGA	4688
rs542054366	snp	A/G	3.29755e-05	0.00406038	intron-variant	NCF2	GRCh38.p7	1:183565794	CCTGAAGGCAACAGG[A/G]AGCGACGGTCAGAAC	4688
rs542077902	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183586515	ATGCATTTTGCTGGG[A/G]TGAAGCCAGGTTTTG	4688
rs542300378	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578963	CACTCCACTCAGTCC[C/T]CTGACCTGGCAGGAA	4688
rs542467571	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183570682	ACTTGAAGGAGCCCT[C/T]ACAATCAGGCAACTC	4688
rs542478605	snp	A/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183577272	AGTGCCAATCAAAAC[A/T]TGCAAATTATCATGA	4688
rs542511325	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578305	CTGCCTCCTCCCTAC[A/G]CTTTGGAAAAGAAAA	4688
rs542643175	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	NCF2	GRCh38.p7	1:183590921	TAGAGTGAGAACTTC[A/T]GTTCCTGTTTGTCTG	4688
rs542683388	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183582275	TCCCCCAGGAGGCAG[C/T]CAAGGTGCTGGCAGC	4688
rs542797677	snp	A/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183577865	AGCAACCCTGAGTCC[A/T]AGTATTCTATACAAC	4688
rs542832503	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183561884	CTCACTGTAACCTCC[A/G]CCTCCTGGGTTCAAG	4688
rs542843755	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183562026	CCAAAGTGTTGGAAT[C/T]ACAGGCATGAGCCAC	4688
rs542947550	snp	A/G			intron-variant	NCF2	GRCh38.p7	1:183567606	TAGTGAGGACTTACA[A/G]TCCTTGCCCTCCCTT	4688
rs542991098	snp	G/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183567587	AAAACCCCACAACAC[G/T]AGATAGTGAGGACTT	4688
rs542995883	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183583371	TCTGAGGGAATTTCT[A/G]TCCCACACATTAAGA	4688
rs543027833	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183575095	ACTGGACAGGTACAG[A/C]GCCGGAAGATGGATC	4688
rs543031906	snp	G/T	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183566761	CCCTCATTCCCAGGT[G/T]CAGCTCTGGGTAGCT	4688
rs543099087	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183576317	AGGGGAAACATTCCT[C/G]CCATGGAACTGTACT	4688
rs543192427	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183559918	CCTGGCTACTAGAGC[A/G]ATAGACAGGGAAAGT	4688
rs543317288	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183589320	ACATTAATAGTTTGG[A/C]ATCTCACTTAATTTT	4688
rs543385874	snp	C/G	0.00358779	0.0422022	intron-variant	NCF2	GRCh38.p7	1:183559118	GCAAGTTGGTGGGCC[C/G]CACCCCAGACCTGAA	4688
rs543577856	snp	C/G			intron-variant	NCF2	GRCh38.p7	1:183570662	CCTCAGCTGCACTGA[C/G]GGCCACTTGAAGGAG	4688
rs543861011	snp	C/T	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183587042	GTGTGAGATGAGCCA[C/T]GGCTCACAGAGCCCT	4688
rs543935249	in-del	-/AGATG	0.311123	0.242413	utr-variant-3-prime	NCF2	GRCh38.p7	1:183555714	TGTCTTGTTTTTGTA[-/AGATG]AGATGCTAGGTTTTT	4688
rs543959946	snp	C/T	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183565571	GGGATTCTGGGGCTG[C/T]GTGGTCATTAGCTGA	4688
rs544019933	snp	A/G	0.000798403	0.0199641	intron-variant	NCF2	GRCh38.p7	1:183580348	GGTACCCAGAAGTAC[A/G]CCAGAAATCAGGTTC	4688
rs544214565	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183578522	GGCGAGCGCCACCAC[A/G]CCCGGCTAATTTTTT	4688
rs544256646	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183563080	GACTTATTACACACC[A/G]TATCCCCAACACCAC	4688
rs544280233	snp	A/C	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183579204	TAACTGGGGGACCCT[A/C]GCAAGTCACTTTCCT	4688
rs544296177	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183562805	ACCCAGCTTGGGCGA[C/T]AGAGTGAGACTCCAT	4688
rs544367843	snp	C/G	0.00795532	0.062565	upstream-variant-2KB	NCF2	GRCh38.p7	1:183591714	TGGTCTCGAACTCCT[C/G]ACCTCAGGTGATTCG	4688
rs544432314	snp	C/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183572447	TCAGCCTCCCAAAGT[C/G]CTGGGATTACAGGCA	4688
rs544453576	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	NCF2	GRCh38.p7	1:183556196	GAAAATGCCCACCTT[C/T]CCTTTGCACTCCCCT	4688
rs544473995	in-del	-/T	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183584564	TGGGACTCACGGGCA[-/T]TTTTTTGGAGGAAAT	4688
rs544535666	snp	C/G	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183557337	TGTGGTGTGACTGGG[C/G]AGCAGTTTTTTCAAA	4688
rs544745512	snp	C/T	0.000131785	0.00811635	missense	NCF2	GRCh38.p7	1:183590241	GGGTCCTGGACGGCA[C/T]TGAAGGCATCCAGGG	4688
rs544821587	in-del	-/A	0.00119737	0.0244387	intron-variant	NCF2	GRCh38.p7	1:183565374	CCCTCAGAGATAAGC[-/A]GGTATAGTTACTTCA	4688
rs544891090	snp	A/G	0.00159617	0.0282053	intron-variant	NCF2	GRCh38.p7	1:183585574	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	4688
rs545215717	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NCF2	GRCh38.p7	1:183590825	GATAGGGGCAGGTCC[C/T]TGGTGAAACCCCACC	4688
rs545412519	snp	C/T	0.00438332	0.0466095	intron-variant	NCF2	GRCh38.p7	1:183581731	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	4688
rs545629061	snp	A/G	0.000399281	0.0141238	intron-variant	NCF2	GRCh38.p7	1:183566597	TGACTACTCTTCCAC[A/G]TGAAGCAGACACACT	4688
rs545693989	snp	C/T	0.00318978	0.0398085	intron-variant	NCF2	GRCh38.p7	1:183557995	TTCTCCTGCCTCAGC[C/T]TCCCAAGGAGCTGGA	4688
rs545709669	snp	C/T			intron-variant	NCF2	GRCh38.p7	1:183581691	TTTTTTTTTTTGAGA[C/T]AGAGTCTCGCTCTGT	4688

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