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

NXF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs4693	snp	A/G	0.494866	0.0504026	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796537	CGACTCTGGAGACCG[A/G]CAAGGGCTCCTGGAT	10482
rs10484	snp	G/T	0.02016	0.0983543	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807115	TTGGCAGCAAAGGGA[G/T]ATGATGCCCTTACCC	10482
rs17644	snp	C/T	0	0	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807133	CCTTTGCTGCCAACG[C/T]TTCCTTTGGGAGAGG	10482
rs489275	snp	C/T	0.0441095	0.141807	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799911	AAGGGTCCCTCTTGG[C/T]GCAAGGGCAAGAGGG	10482
rs490791	snp	A/C	0	0	intron-variant	NXF1	GRCh38.p7	11:62803673	TAAGACTGTTTAATC[A/C]CTAAGCTAGTCCTGG	10482
rs529220	snp	C/T	0.148326	0.228391	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806009	TTTATTTCACAAATA[C/T]ATGTTGAGTTTTTAC	10482
rs539465	snp	C/T	0.0161686	0.088447	intron-variant	NXF1	GRCh38.p7	11:62795881	GAATCTTTAGAGTCC[C/T]GAGTTTGTAGCGTGG	10482
rs561520	snp	A/G	0.0441095	0.141807	intron-variant	NXF1	GRCh38.p7	11:62803148	atacagtgaaacccc[A/G]tctctactaaaaata	10482
rs595108	snp	C/G	0.0482946	0.147699	intron-variant	NXF1	GRCh38.p7	11:62795763	GGTAGGCCAAGCCAA[C/G]ACGGCTTGGGGGCAG	10482
rs631310	snp	C/T	0.314787	0.241459	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800164	CACAGACCCAGCAAA[C/T]AGATAGTCAAGTCAG	10482
rs1815870	snp	C/G	0.177841	0.23936	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792779	TTGTTGGCAAACTTG[C/G]GTGCTTTTATGGAGT	10482
rs2298634	snp	C/T	0.000298097	0.0122049	intron-variant	NXF1	GRCh38.p7	11:62795869	CTGGGGGTGGGACCA[C/T]GCTACAAACTCGGGA	10482
rs2509681	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62798436	CTTTTTTTTTTTTTT[A/T]TTTGAGACGGAGTTT	10482
rs2509682	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62798428	tttttttttttgaga[C/T]ggagtttcactcgtc	10482
rs2584918	snp	A/G	0.216933	0.247804			GRCh38.p7	11:62791913	CGGCCCCTGCAAGGC[A/G]CGACGCTGCAACGGG	10482
rs2850598	snp	C/G	0	0	intron-variant	NXF1	GRCh38.p7	11:62798240	gggtttcaccatgtt[C/G]gccaggctggccttg	10482
rs2956139	snp	A/G	0.0238507	0.106567	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791829	TTCTGCGCGGGCCAG[A/G]GCGTCTTCTGGGCTT	10482
rs3017667	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62803173	caccaccacgcccgg[C/G]taatttttgtatttt	10482
rs3763851	snp	A/C	0.430285	0.173197	intron-variant	NXF1	GRCh38.p7	11:62804961	CCCGAGAGTTCAAGA[A/C]CGACTGGACGCAGTA	10482
rs3881262	snp	C/T	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799936	CTTCCCTCCTTTGTA[C/T]TGTGATGGCCCCTCT	10482
rs5792271	in-del	-/TTTT	0.212425	0.24716	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793083	TGTTTTTCTGTTTGC[-/TTTT]TTTTTTTTTTTGAGA	10482
rs7105855	snp	C/T	0.273049	0.248935	intron-variant	NXF1	GRCh38.p7	11:62796941	GTGCAGTGGCACACA[C/T]CTGTAGTCCCAGCTA	10482
rs10897294	snp	A/G	0.169435	0.236663	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806406	ACACTAATCTCCCTG[A/G]ACGGTGGGTATTCTG	10482
rs11231221	snp	C/T	0.244722	0.249944	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792029	TGGGGCTTCCTGCCG[C/T]AGAGCCGCCTTCCGC	10482
rs11231224	snp	G/T	0.00956916	0.0685055	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806493	ATCAAAAGCCTCAAC[G/T]GGAGTTGGGAACAAA	10482
rs11557825	snp	C/T	0.0109286	0.0731087	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807264	CTCAGGCCTATGAAA[C/T]ACACAGGGTTCTAGA	10482
rs12225338	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806462	TGGCTTTGATTTGGT[A/G]AAGTGCTTGGAGGGA	10482
rs12365081	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807106	CAGGAAGGTGGGTAA[A/G]GGCATCATCTCCCTT	10482
rs12796555	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798881	CCCCCCTTACCTTCC[A/C]CCTACTCACCTGTGC	10482
rs28400288	snp	A/G	0.0271762	0.113356	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793313	TGATCTCTTGACCTC[A/G]TGATCTGGCCGCCTC	10482
rs34443315	in-del	-/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799834	ATTGCATGCCACCAG[-/C]CCCTAGGAGGCCTCA	10482
rs34495263	in-del	-/A	0.306182	0.243605	intron-variant	NXF1	GRCh38.p7	11:62798127	AGCAAGACTCCATCC[-/A]AAAAAAAAAAAAAAA	10482
rs34626575	snp	A/G	0	0	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801358	CTTCAATGATCCTCA[A/G]GGTAGCTGCCATACA	10482
rs34865507	in-del	-/T			intron-variant	NXF1	GRCh38.p7	11:62795537	CCCCAGGCCAAGCAC[-/T]TTTGTAAGTCACTTC	10482
rs35296297	in-del	-/A			intron-variant	NXF1	GRCh38.p7	11:62802914	CTCCCTCCCCCAACC[-/A]AAATTTTCATATTTC	10482
rs35447429	in-del	-/A			intron-variant	NXF1	GRCh38.p7	11:62804237	AGAAGCAGGATGTAG[-/A]AAATGTGAGACCCAA	10482
rs35839700	in-del	-/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799736	CGCCTGCTGGCGGGG[-/C]CCCCAGCTCTGGTCA	10482
rs56389050	in-del	-/A			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793843	AAAAAAAAAAAAAAA[-/A]TACAAAAATTAGCCA	10482
rs56994557	snp	A/G	0.0441095	0.141807	intron-variant	NXF1	GRCh38.p7	11:62802100	AGCCCTTGGGGAGGG[A/G]CATTACGCTGGGAGT	10482
rs61088491	snp	A/G	0.0551013	0.156571	intron-variant	NXF1	GRCh38.p7	11:62804550	ATGACCTTCTGATTC[A/G]TGCTGTGTAGGACTG	10482
rs61893770	snp	A/G	0	0	intron-variant	NXF1	GRCh38.p7	11:62798146	AAAAAAAAAAAAAGG[A/G]CCTGGTGCGAGTGGC	10482
rs71056564	in-del	-/T	0	0	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793097	TTTTTTTTTTTTTTT[-/T]GAGACCGAGTCTTGC	10482
rs71458435	in-del	-/T	0.5	0	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793082	TGTTTTTCTGTTTGC[-/T]TTTTTTTTTTTTTTT	10482
rs71458436	in-del	-/A	0.5	0	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793820	AAGCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA	10482
rs71458437	in-del	-/T	0.5	0	intron-variant	NXF1	GRCh38.p7	11:62803289	CACTGTACTCCAGCC[-/T]TGGGTGACAGAGCAA	10482
rs73485689	snp	A/G	0.0562307	0.157967	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799238	GGGAGAAAAGGGAGA[A/G]AGACACCCTGACACA	10482
rs74449247	snp	A/G	0.0232847	0.105357	intron-variant	NXF1	GRCh38.p7	11:62794814	TTAACTACTATGTGA[A/G]CTTTCTCTGATTTCC	10482
rs74814035	snp	C/T			missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801158	ATGCTAGACATGTCA[C/T]CCAGCCTGTACAGCC	10482
rs75592862	snp	A/G	0.00874735	0.0655527	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805431	ACTCCCAAGCGCTCA[A/G]GACCGAAGTGTCCCT	10482
rs76498401	snp	A/C/G	0.00304137	0.0388786	intron-variant	NXF1	GRCh38.p7	11:62797166	GGGGTGGGGAGGGGG[A/C/G]ACCCTGGGATACTTA	10482
rs76934823	snp	A/G	0.0128488	0.0791159	intron-variant	NXF1	GRCh38.p7	11:62796433	AAACCCAGTGGTCCC[A/G]GGCAGATTCTGGGAT	10482
rs77243807	snp	A/C	0.5	0	intron-variant	NXF1	GRCh38.p7	11:62802758	CACTTATAATCTCTC[A/C]AAAAAAAATCAATTT	10482
rs77403482	snp	A/G	0.00488826	0.0491959	intron-variant	NXF1	GRCh38.p7	11:62803611	TGACCACAAATGCTA[A/G]GAAAGTCTTCTCAAA	10482
rs77610501	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798939	AGCCCAGGGGCTCCG[A/C]TGCCTCACCAGGTAT	10482
rs77618759	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794091	AGGACAGCTTGTGCC[C/T]AGGAATTAGAGGCTA	10482
rs77993038	snp	A/G	0.0142736	0.0832652	intron-variant	NXF1	GRCh38.p7	11:62802770	CTCAAAAAAAAATCA[A/G]TTTTATTTATTCTAA	10482
rs78194278	snp	A/T	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62795832	GTAGCTGGGAAGCTA[A/T]GAGTGCTGAGGAAAA	10482
rs78433686	snp	C/T	0.0337553	0.125452	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794764	GGATGAAAACCCAGA[C/T]GGTACAATTCCAGAG	10482
rs78694490	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794689	AAACTTAGGAAATGA[A/G]TATTGTTATATGAAT	10482
rs78829240	snp	A/G	0.0232847	0.105357	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806268	CTCCTAGACCCCCAA[A/G]AGCACCACCACCAGC	10482
rs79134972	snp	A/G	0	0	intron-variant	NXF1	GRCh38.p7	11:62798143	AAAAAAAAAAAAAAA[A/G]GGGCCTGGTGCGAGT	10482
rs79324007	snp	C/T	0.00676061	0.057746	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792778	CACTCCATAAAAGCA[C/T]CCAAGTTTGCCAACA	10482
rs111331941	in-del	-/C	0.5	0	intron-variant	NXF1	GRCh38.p7	11:62797084	AAAAAAAAAAAAAAA[-/C]AAAACAAAAAACAAA	10482
rs111401731	snp	A/C/G	0.00183264	0.0302156	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805374	CACAGCGAAGATCAA[A/C/G]GGCGGGCTCAGGCGC	10482
rs111684491	snp	A/C	0.5	0	utr-variant-3-prime, missense, upstream-variant-2KB, intron-variant	NXF1, MIR6514	GRCh38.p7	11:62794424	GCACAAATAGCTCAT[A/C]ATTTACAATACATAG	10482
rs111950515	snp	A/C	0.0414363	0.137845	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805476	CGCATTTATACAGCA[A/C]AGCACGTCGCGCGCC	10482
rs111966744	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793563	ATGCCTGTAGTCCCA[G/T]CTACTCAGGTGGCTG	10482
rs112043892	snp	A/C/G	1.64735e-05	0.00286993	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792455	TTTACAGGGGGGACT[A/C/G]CTTCTGAGGCATGAC	10482
rs112335937	snp	A/T	0.000273075	0.0116817	intron-variant	NXF1	GRCh38.p7	11:62804175	GGGAAAAGTTACTGG[A/T]AAACTGTGTAGGGCT	10482
rs112714659	in-del	-/CTAACATTC	0.5	0	intron-variant	NXF1	GRCh38.p7	11:62804678	ACATAGAAGGCGCAG[-/CTAACATTC]ACTGAGAACTTTCTC	10482
rs112813447	snp	C/T	0.5	0	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805499	CGCGCGCCGCTGACG[C/T]CCCAGGCTGTGGGCG	10482
rs113286052	snp	C/G	0.5	0	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62805348	GTACGACTTCCCCTC[C/G]TCCGCCATGCCACAG	10482
rs113503642	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793610	TGAGCCCTAGCAGTT[A/G]AGGCTGCAGTGAACT	10482
rs113557276	snp	A/C	0.5	0	intron-variant	NXF1	GRCh38.p7	11:62797089	AAAAAAAAAACAAAA[A/C]AAAAAACAAAACAAA	10482
rs113601386	snp	C/T	0.444444	0.157135	intron-variant	NXF1	GRCh38.p7	11:62797144	CCCACCATTCCCCCT[C/T]AACCTCGGGGTGGGG	10482
rs113901554	snp	G/T	0.00115245	0.023977	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792527	GGCCTGGAGAAAAAT[G/T]AAGGTCAGTAGAGGT	10482
rs113993569	snp	C/T	0.444444	0.157135	intron-variant	NXF1	GRCh38.p7	11:62804544	AGGAAGATGACCTTC[C/T]GATTCATGCTGTGTA	10482
rs114333528	snp	A/G	0.00196523	0.0312851	intron-variant	NXF1	GRCh38.p7	11:62802164	CCAGCCAGCCACTCA[A/G]GCCTTGTCTTACCTC	10482
rs114397144	snp	A/C	0.0158469	0.0875917	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799268	AGCCCTTTCTTTCAG[A/C]TGCCCCATCCCTGTG	10482
rs114976329	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807107	AGGAAGGTGGGTAAG[A/G]GCATCATCTCCCTTT	10482
rs115224284	snp	C/T	0.0185938	0.0946107	intron-variant	NXF1	GRCh38.p7	11:62797818	GAAGTCAAGTGTAAA[C/T]GCATCATGAAAAGTA	10482
rs115432554	snp	C/T	0.0532157	0.154195	intron-variant	NXF1	GRCh38.p7	11:62802831	GCCCCTCAGAGAACT[C/T]CAGGGCACTCCAGGG	10482
rs115702320	snp	A/G	0.00716266	0.059414	intron-variant	NXF1	GRCh38.p7	11:62803678	CTGTTTAATCACTAA[A/G]CTAGTCCTGGCATTT	10482
rs116085107	snp	A/T	0.0228947	0.104514	intron-variant	NXF1	GRCh38.p7	11:62803323	TCCATTTAAAAAAAA[A/T]AATAATAATAATTTT	10482
rs116591122	snp	G/T	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62804599	CTAACTCCCAAAAGA[G/T]GTCTGCCTAATACCC	10482
rs116823129	snp	A/C	0.00597247	0.0543191	intron-variant	NXF1	GRCh38.p7	11:62804474	AATTCTAGACTCAGG[A/C]TCTAGTGGCAGTGCC	10482
rs117263999	snp	C/T	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62795998	AGAGCCTGAGTGCCC[C/T]CCCTTGCCTATTAAA	10482
rs117327300	snp	C/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62800824	GCTCAGGCTAGAATG[C/G]AACGGCACAATCATA	10482
rs118167825	snp	C/T	0.0641038	0.16716	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791879	AAGCGGCCCCGATCA[C/T]GCTCAAAGAGCAGCA	10482
rs138084535	snp	C/G/T	1.648e-05	0.0028705	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803907	TACGGTTTCCTTCAC[C/G/T]ATATTTCCACCGGAA	10482
rs138160443	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792874	GTTCTACCAATGGCT[C/T]CTCAAAGATAAGGAA	10482
rs138193807	snp	C/G/T	9.90437e-05	0.00703659	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794271	ACTTCTGGGACCACT[C/G/T]GAGGTTCATGCCAGA	10482
rs138285302	snp	C/T	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62800564	TACCCCCAGTCCCTA[C/T]GCTTAGCTCTGAGAT	10482
rs138988501	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800132	AAAAGGTTGTGTTCA[G/T]GAAGAAAGAGAAAGG	10482
rs139081574	snp	A/G	0.000198778	0.00996741	intron-variant	NXF1	GRCh38.p7	11:62795859	AAAATTCCAGCTGGG[A/G]GTGGGACCACGCTAC	10482
rs139190483	snp	C/T	0.0146672	0.084371	intron-variant	NXF1	GRCh38.p7	11:62805049	GTCAGGCCGCCAAAC[C/T]TAACTGACAGGCATC	10482
rs139389102	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793558	GGCCTATGCCTGTAG[C/T]CCCAGCTACTCAGGT	10482
rs139771808	snp	A/C	3.29457e-05	0.00405854	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797348	CGTCGTGGGGGCTTC[A/C]ACATCAAAGGCAATT	10482
rs139794879	snp	C/T	0.00487104	0.04911	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803841	TTGCCACATCTCCAT[C/T]ATCTTCCTCAAGGCG	10482
rs139996469	snp	A/C/G	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62797689	CCAGCCTGGATGACA[A/C/G]AGCCAGACCCTGTCT	10482
rs140258993	snp	G/T	0.000412191	0.0143501	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62795938	AGAAAAACACAGCAA[G/T]GTGCTCTGAAAGAGA	10482
rs140528299	snp	A/C/G	1.64743e-05	0.00287	NXF1	11	allele_origin=G(germline)/A(somatic)	11:62801626	GTATCGTTTGCTCAT[A/C/G]ATCAGCTAGAGGAAA	10482
rs140912061	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801563	GCTGTCAACCATACC[C/T]GGGTCTGAACGGAGG	10482
rs141213729	snp	A/G	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794638	TAGGGTTCTCCCAAC[A/G]CATGGACTTTAGCTC	10482
rs141871584	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800269	AAAGGACAGGTGGTT[C/T]CAGCTCAGGGCTGCA	10482
rs141910936	in-del	-/GAAAG	0.0566069	0.158427	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799074	GAGGCAAAGGAATAA[-/GAAAG]GAAAGGAAAAGGAGG	10482
rs142398478	snp	C/T	0.000247066	0.0111118	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797327	TCCTACCTTGCAGGG[C/T]GGTAACGTCGTGGGG	10482
rs142420430	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799150	GGAGGTATAGGAGAC[A/G]GACAGAAAAAGGAAA	10482
rs142434559	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805919	TGAGAATTAGAATGT[A/G]AGCTCGAACGTTGAC	10482
rs142453256	snp	C/T	0.0444908	0.142359	intron-variant	NXF1	GRCh38.p7	11:62803209	CTGTAGTCCCAGCTA[C/T]TCGGGAGACTGAGGC	10482
rs142603731	snp	A/G	0.00177763	0.02976	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798587	GGCGCTGTCAAGAAC[A/G]GGACAGAAGTGAGTG	10482
rs143310652	snp	A/C	0.0524604	0.153226	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793765	GAGGTAGGCAGATCA[A/C]AAGGTCAGGAGTTCG	10482
rs143444714	snp	C/T	0.000642277	0.0179088	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794341	AGAGAGGGTGGGCAC[C/T]GGGCTGGAGGAAGGC	10482
rs143505327	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62804778	ACACTCTTAAGAAAT[A/G]CTGTTGTTATTCCAC	10482
rs143742098	snp	C/G	1.66001e-05	0.00288094	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803976	CGCGTTCATCATCGT[C/G]TTCTAGAGTTAGAAA	10482
rs144470477	snp	A/G	0.00133345	0.0257866	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796333	ATCCTTGAAATACTC[A/G]GCTAAGCTGCTTCTG	10482
rs144471031	snp	A/G	4.95021e-05	0.0049748	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801115	TCCAGAAAGGTTTAG[A/G]ATCTTCAGGTTGGGT	10482
rs145757652	snp	A/G	0.000181185	0.00951628	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803517	CAGTAACATGAATGC[A/G]ATCTCGATCATGCCA	10482
rs145936894	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797495	GCTTGAGCTCAGGAG[C/T]TTGAGACCAGCCTGG	10482
rs146333276	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793481	CTTTGGGAGGCCTAG[C/G]TGGGCAACATGGTGA	10482
rs146456664	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799941	GGCCATCACAGTACA[A/T]AGGAGGGAAGGCCCA	10482
rs146549860	snp	C/T	3.29902e-05	0.00406128	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801199	CAAGTTCAAGGACAA[C/T]AGCTGTGAGGAGAGA	10482
rs146787397	in-del	-/AC	0.138562	0.223789	splice-acceptor-variant	NXF1	GRCh38.p7	11:62801633	TGCTCATGATCAGCT[-/AC]AGAGGAAAAAGAAGG	10482
rs146887127	snp	A/G/T	0.000592851	0.017207	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797339	GGGCGGTAACGTCGT[A/G/T]GGGGCTTCAACATCA	10482
rs147085267	snp	A/C/G			missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802257	ACTTTCTGCCATAAG[A/C/G]AATCTAGAAATGAGA	10482
rs147145490	snp	A/G	0.000198177	0.00995234	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62795003	ATCCCGGGACTTTCC[A/G]TCCACTGCAATAAGA	10482
rs148018473	snp	C/T	0.0126979	0.078662	intron-variant	NXF1	GRCh38.p7	11:62803179	CAAAAATTAGCCGGG[C/T]GTGGTGGTGGGTGTC	10482
rs148869039	snp	A/T	0.00517822	0.0506191	intron-variant	NXF1	GRCh38.p7	11:62798300	AGGTGTGGTAGCACA[A/T]GCCTGTAATCCCAGC	10482
rs148886422	snp	G/T	9.88354e-05	0.00702908	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803535	CTCGATCATGCCAAG[G/T]ATCACCCCGACGGTT	10482
rs149145223	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793224	GTTGGGACTACAGGC[C/G]TGGAACGCCAAGCCC	10482
rs149273641	snp	C/T	0.000872852	0.0208726	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796115	ACGTCGTGCTGGGTT[C/T]TGGGCAACTCATTGA	10482
rs149622184	snp	C/G/T	0.00248674	0.035175	intron-variant	NXF1	GRCh38.p7	11:62801076	CTTCAAAAATATAGC[C/G/T]GAGCTATCAATTCTC	10482
rs150232290	snp	A/G	0.000181185	0.00951628	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801611	TTGTTGGGAGCCATC[A/G]TATCGTTTGCTCATG	10482
rs150387479	snp	A/G	8.23608e-05	0.00641667	upstream-variant-2KB, utr-variant-3-prime, synonymous-codon, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792506	CACTTCTGGGATCTC[A/G]CCCTTGGCCTGGAGA	10482
rs150419656	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792587	CTCAGCTAACCTGAC[A/C]TCCTGGAGGCCCAGA	10482
rs150474222	snp	C/T	0.0208331	0.0999127	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800291	AGGGCTGCACATCTC[C/T]GCAGACGGGCCCTGG	10482
rs150662281	in-del	-/T	0.0547245	0.156101	intron-variant	NXF1	GRCh38.p7	11:62802840	AGAACTCCAGGGCAC[-/T]CCAGGGACTCCAAGC	10482
rs150738203	snp	C/T	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62795346	CTGGGCGTGGTAGTG[C/T]GCACCTGTAGTCCCA	10482
rs150805268	snp	C/G	0.00199481	0.0315187	intron-variant	NXF1	GRCh38.p7	11:62804803	TTCCACATTAAGGGG[C/G]TGGAAAACGAGAGTT	10482
rs151071893	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799026	CACAGGATGTTGGGG[C/T]AGGGAGATGAGCAGG	10482
rs151183155	snp	G/T	0.00144863	0.0268741	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792434	GACGGTAATATCCAA[G/T]GACTATTTACAGGGG	10482
rs180922789	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799069	AGAGGAGAGGCAAAG[A/G]AATAAGAAAGGAAAA	10482
rs181132531	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798165	GGTGCGAGTGGCTCA[C/T]GTCTGTAATCCCAGC	10482
rs181325349	snp	A/G	3.30011e-05	0.00406195	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794272	CTTCTGGGACCACTC[A/G]AGGTTCATGCCAGAC	10482
rs181532360	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806785	GTGTCAGCAGTGATA[A/C]CTGGCAGAGCCATTA	10482
rs181928635	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62795199	AGTAATAACTACGGC[C/T]GGGCACAGTGTCTCA	10482
rs182070458	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794661	TTTAGCTCTTTTAAT[G/T]CATCCTCACAACAAA	10482
rs182237849	snp	A/G	0.00279162	0.0372561	intron-variant	NXF1	GRCh38.p7	11:62803265	AGGCTGCAGTGAGCC[A/G]AGATCACGCCACTGT	10482
rs182572262	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798715	CCCAGCCTGTGCTCA[A/G]GGAAAAATGGCCCCC	10482
rs182678917	snp	C/G/T	0.00204142	0.0318845	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791955	GGGGCCGCAGCACGG[C/G/T]TAGCAGCCCCGTGGG	10482
rs182803957	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62795765	TAGGCCAAGCCAAGA[C/T]GGCTTGGGGGCAGAA	10482
rs182934842	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807319	CCAGAGGCAAGGGGT[A/G]GGGGATCAGGGGCAG	10482
rs182975997	snp	A/T	0.00716266	0.059414	intron-variant	NXF1	GRCh38.p7	11:62800792	TTTAAATTAAAAAAA[A/T]TTTTTTGAGACAGGT	10482
rs183380305	snp	A/C/G	4.942e-05	0.00497071	intron-variant	NXF1	GRCh38.p7	11:62801669	GTGGTCACTGGGTTT[A/C/G]TGTGTGGGGGGTGGG	10482
rs183522283	snp	A/G	0.00358779	0.0422022	intron-variant	NXF1	GRCh38.p7	11:62797994	AGAAATTAGCCGGGC[A/G]TTGTGGCACATGCCT	10482
rs183706989	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796796	AAAAATGGCTAGGTG[C/T]GGTGGCTCACGCCTC	10482
rs183916343	snp	A/G	3.3691e-05	0.00410419	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794474	TTAAAAAGCTAGACA[A/G]AGATAACATCATCCT	10482
rs184434268	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806039	ATGAATTTGTGTTAT[C/G]AATTTCCCCCACCCC	10482
rs184478520	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793893	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGATTG	10482
rs184728477	snp	A/G	0.00636936	0.0560724	intron-variant	NXF1	GRCh38.p7	11:62805012	GCCCACGAGCAGGGC[A/G]CTCACTCACATTAAA	10482
rs185052975	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792943	AGTGGTAGGGAAAGA[C/T]GTTCATGGTGTAAGT	10482
rs185144328	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799142	AGAGATGGGGAGGTA[C/T]AGGAGACAGACAGAA	10482
rs185297420	snp	A/C	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798180	CGTCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA	10482
rs185488476	snp	A/C	0.00716266	0.059414	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806578	GGAAGAATTACGGCC[A/C]AATAGTTGGAGGATA	10482
rs185505524	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795217	GCACAGTGTCTCATG[C/T]GTATAATCCCAGCAC	10482
rs185516228	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797110	ACAAAACAAAAAGAT[C/T]GATGTGTGCCTGGGT	10482
rs185710797	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807366	TTCCAGGGAAACAGG[A/G]CCTTTCTCCCAAGTA	10482
rs186266057	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807000	TGCAGGCAGCTGAAG[A/G]GCTCAGGGCTCCCTG	10482
rs186397328	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798870	TCCCCTCCCTGCCCC[C/G]CTTACCTTCCACCTA	10482
rs186604742	snp	C/T	0.00159617	0.0282053	intron-variant	NXF1	GRCh38.p7	11:62794809	GGCTCTTAACTACTA[C/T]GTGAGCTTTCTCTGA	10482
rs186773519	snp	C/G	0.00159617	0.0282053	intron-variant	NXF1	GRCh38.p7	11:62797600	AGTCCTAGCTACTTG[C/G]GAGGCTGAAGTGGGA	10482
rs187090821	snp	C/T	0.00795532	0.062565	intron-variant	NXF1	GRCh38.p7	11:62795839	GGAAGCTAAGAGTGC[C/T]GAGGAAAATTCCAGC	10482
rs187131549	snp	G/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800809	TTTTTGAGACAGGTT[G/T]CTCAGGCTAGAATGC	10482
rs187442274	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62804281	CACAAATCAGACCTC[C/T]GAAAGCCACCTGAAA	10482
rs187661734	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	TMEM223, NXF1	GRCh38.p7	11:62792126	CAGCACGCAGAACAC[C/G]AAATACAACATCACT	10482
rs187838681	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62802836	TCAGAGAACTCCAGG[C/G]CACTCCAGGGACTCC	10482
rs188140949	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793960	GAGCCAAGATCGCAC[C/T]ACTGCACTCCAGCCT	10482
rs188175128	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796961	AGTCCCAGCTACTGG[C/G]GAGGCTGAGGCAGGA	10482
rs188403281	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799031	GATGTTGGGGCAGGG[A/G]GATGAGCAGGTGGGG	10482
rs188609830	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798047	CTGAGGCAGGAGAAT[C/T]ACTTGAACCCAGGAG	10482
rs189044057	snp	C/T			intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794537	ATATCCACAAGGTCC[C/T]CCTCCCACTCTTAGC	10482
rs189125050	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806700	AGGAAGTTTCCACGC[C/T]AATGAAGTGTTGCAA	10482
rs189494684	snp	A/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806339	GTATGAGACAGGGGC[A/T]CTCGAGTGACCTCAG	10482
rs189822309	snp	C/T	0.00755907	0.0610114	intron-variant	NXF1	GRCh38.p7	11:62795368	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG	10482
rs189976833	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798688	CCCATCCTGCTCATC[C/T]CTCCACTCCCTCCCA	10482
rs190257933	snp	G/T	0.00266147	0.036382	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791912	TCCCGTTGCAGCGTC[G/T]TGCCTTGCAGGGGCC	10482
rs191034414	snp	A/G	0.000148279	0.00860914	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796102	CACGAAGGAATTGAC[A/G]TCGTGCTGGGTTTTG	10482
rs191187362	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797675	TGTGCCACTGCACTC[C/T]AGCCTGGATGACAGA	10482
rs191308594	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807242	TCACTTCACAGCAGA[A/G]TTCAAATCTAGAACC	10482
rs191423180	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800245	AAGTGGGGAGCACGC[A/G]ATCCTCTCAAAGGAC	10482
rs191516295	snp	C/G	0.00751267	0.0608268	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801631	GTTTGCTCATGATCA[C/G]CTAGAGGAAAAAGAA	10482
rs192101820	snp	G/T			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792383	AGTCACGGGGCGGCC[G/T]CGGGCCAGACAGGAG	10482
rs192331386	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795066	TATGTTTACAAACAG[C/T]TTCTTGAATCATGGT	10482
rs192364184	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803150	ACAGTGAAACCCCGT[C/T]TCTACTAAAAATACA	10482
rs192863630	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805432	CTCCCAAGCGCTCAG[A/G]ACCGAAGTGTCCCTA	10482
rs193006967	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804853	CTCCACCACGCACTC[C/T]TAACTTACTACAAAG	10482
rs193015471	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793890	CCTGTAATCCCAGCT[A/G]CTCGGGAGGCTGAGA	10482
rs193297263	snp	C/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62796992	GAATCACTTGAACCC[C/T]GGGAGGCAGAGGTTG	10482
rs199600277	snp	A/C/T	0.000559933	0.016723	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792550	GTAGAGGTAGGCCTA[A/C/T]CCTCGCCACTCAGCA	10482
rs199769585	snp	C/G	0.00039527	0.0140527	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801565	TGTCAACCATACCTG[C/G]GTCTGAACGGAGGCC	10482
rs199773758	snp	A/T	0.00121374	0.0246048	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791795	ACCGGGGGCCGGGAC[A/T]CGGCTGCCACAGCCA	10482
rs199915757	snp	A/G	0.000151964	0.00871544	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792743	TAAGAACTCTGACTC[A/G]TAAATGCCAGCTGAA	10482
rs199953482	snp	A/C/G	0.000134144	0.00818873	intron-variant	NXF1	GRCh38.p7	11:62801077	TTCAAAAATATAGCC[A/C/G]AGCTATCAATTCTCA	10482
rs199956847	snp	A/G	3.29451e-05	0.00405851	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797337	CAGGGCGGTAACGTC[A/G]TGGGGGCTTCAACAT	10482
rs199977893	snp	A/G	9.88386e-05	0.00702919	intron-variant	NXF1	GRCh38.p7	11:62801539	ATCACCACCTATCTG[A/G]GAACTACTGCTGTCA	10482
rs200039111	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803212	TAGTCCCAGCTACTC[A/G]GGAGACTGAGGCAGA	10482
rs200044819	snp	A/C	0.000131848	0.00811828	intron-variant	NXF1	GRCh38.p7	11:62796223	GTGCTGCCACACACT[A/C]CTGAGTTCTGACTGA	10482
rs200187006	snp	C/G	0.000101348	0.00711784	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805385	TCAAGGGCGGGCTCA[C/G]GCGCTGGCCGCTACG	10482
rs200223907	snp	A/G	0.006903	0.0583425	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791966	ACGGCTAGCAGCCCC[A/G]TGGGCCATCGCCTCC	10482
rs200296358	snp	C/T	1.65225e-05	0.00287419	intron-variant	NXF1	GRCh38.p7	11:62794932	GAAAAGCAGAATACT[C/T]ACCCTGAATTGCTAG	10482
rs200303541	snp	C/T	4.96512e-05	0.00498228	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803961	TTTGAGGGAAATTAA[C/T]GCGTTCATCATCGTG	10482
rs200323908	in-del	-/AG	0.0119091	0.0762411	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799182	AGAAAGCAAAGAAAA[-/AG]AGAAAGAACTACAAG	10482
rs200473809	snp	A/G	0.000148249	0.00860829	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801986	AGTTGACAGCCTTCA[A/G]TGCAGAGGCAGTACT	10482
rs200532224	snp	C/G/T	1.65034e-05	0.00287253	intron-variant	NXF1	GRCh38.p7	11:62803390	GCCTCCTATCTCTAC[C/G/T]GTACCATCTACTTTC	10482
rs200567319	snp	A/C			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793846	AAAAAAAAAAAAATA[A/C]AAAAATTAGCCAGGC	10482
rs200588581	snp	A/C/G/T	0.000225881	0.0106255	synonymous-codon, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800334	AGCTCAGCCTCCCAG[A/C/G/T]GGGTGAAGGTCCCCA	10482
rs200629020	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792635	CACTGTATTTCCAGA[A/C/T]CTTACCTTGAGATGA	10482
rs200741992	snp	C/T	3.29989e-05	0.00406182	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801381	GCCATACAGCTTCTG[C/T]GATTCAGGACAACGT	10482
rs200828406	snp	C/T	0.00115257	0.0239782	intron-variant	NXF1	GRCh38.p7	11:62796368	AATAAAAGGAATGGA[C/T]GTGGTGTTCAGAGCA	10482
rs200856666	snp	C/T	4.95471e-05	0.00497705	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803945	CGGCCTTTCTTCTTT[C/T]TTTGAGGGAAATTAA	10482
rs200911666	snp	C/T	0.001191	0.0243737	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791903	AGCAGCACATCCCGT[C/T]GCAGCGTCGTGCCTT	10482
rs200919758	snp	C/T	9.88452e-05	0.00702942	intron-variant	NXF1	GRCh38.p7	11:62797281	GGAAGCAGTATTCTC[C/T]CCACACACAAGTTCT	10482
rs200954542	snp	A/G	0.000549994	0.0165739	intron-variant	NXF1	GRCh38.p7	11:62802287	AGAAAGAGAAAAGAA[A/G]GGAATGATAAGTAAG	10482
rs201179821	snp	C/T	0.00014843	0.00861354	intron-variant	NXF1	GRCh38.p7	11:62803602	AGAATAAAATGACCA[C/T]AAATGCTAGGAAAGT	10482
rs201274833	snp	G/T	1.67223e-05	0.00289151	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794459	GAGGACAAAGAGCAC[G/T]TAAAAAGCTAGACAG	10482
rs201365858	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795777	AGACGGCTTGGGGGC[C/T]GAATGGGAGAAGGAG	10482
rs201490270	snp	C/T	0.000675192	0.0183614	intron-variant	NXF1	GRCh38.p7	11:62796456	TCTGGGATGTGATAC[C/T]AACCGGGCAGGGTTC	10482
rs201523289	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798599	AACGGGACAGAAGTG[A/T]GTGATGCTTCAGAGC	10482
rs201533876	snp	A/G	0.000527027	0.0162245	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794374	GGGTGCAGGCATAGC[A/G]AAGGCTCTTTGGATC	10482
rs201573295	snp	A/G	0.00296688	0.038401	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791933	TGCAGGGGCCGGCAG[A/G]TGAGCAGGGGCCGCA	10482
rs201574995	snp	A/G	0.00199806	0.0315443	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802181	CCTTGTCTTACCTCA[A/G]TAGGGGTGAAGGGCA	10482
rs201668206	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804949	CCAAAGCCCAGGCCC[A/G]AGAGTTCAAGACCGA	10482
rs201844884	snp	A/G	0.00299544	0.0385843	intron-variant	NXF1	GRCh38.p7	11:62796220	GTGGTGCTGCCACAC[A/G]CTCCTGAGTTCTGAC	10482
rs201901987	snp	C/T	3.29489e-05	0.00405874	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801780	TCAGTTCATTCAGTA[C/T]AGTGTGGGGTGGAGC	10482
rs201907886	snp	A/T	0.00136467	0.0260859	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791800	GGGCCGGGACACGGC[A/T]GCCACAGCCATGGAA	10482
rs202162439	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803544	GCCAAGTATCACCCC[A/G]ACGGTTAGGTCGGGT	10482
rs202220238	snp	G/T			intron-variant	NXF1	GRCh38.p7	11:62804388	TCTCCTTGTTCTCAA[G/T]CTGCCACTTTGAAGT	10482
rs267603079	snp	A/G			missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803925	ATTTCCACCGGAAGG[A/G]ACCCCGGCCTTTCTT	10482
rs367658652	snp	C/T	1.65135e-05	0.00287341	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62795002	AATCCCGGGACTTTC[C/T]GTCCACTGCAATAAG	10482
rs367889111	snp	C/T	4.94222e-05	0.00497078	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792427	ACAACCAGACGGTAA[C/T]ATCCAAGGACTATTT	10482
rs367896170	snp	A/C	6.76053e-05	0.00581361	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805405	TGGCCGCTACGCCGG[A/C]AAACAACCTAACTCC	10482
rs367975743	snp	C/T	4.94189e-05	0.00497062	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796332	TATCCTTGAAATACT[C/T]GGCTAAGCTGCTTCT	10482
rs368015936	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802791	TTTATTCTAAAAGTT[C/T]CAAGATATTATTTAC	10482
rs368133822	snp	A/C	1.6571e-05	0.0028784	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796556	TCTCCAGAGTCGTAA[A/C]TTGCATAGTACCTAT	10482
rs368347875	snp	A/G	5.03402e-05	0.00501673	intron-variant	NXF1	GRCh38.p7	11:62797151	TTCCCCCTCAACCTC[A/G]GGGTGGGGAGGGGGG	10482
rs368360143	snp	C/T			synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801136	CAGGTTGGGTGCCTT[C/T]TGAACAATGCTAGAC	10482
rs368363885	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794287	GAGGTTCATGCCAGA[C/T]TGGGTAGAGAATGCT	10482
rs368425962	snp	A/T	8.24124e-05	0.00641868	intron-variant	NXF1	GRCh38.p7	11:62803580	AGGGGTTGCTGTGGG[A/T]AAGCAGAGAATAAAA	10482
rs368493809	snp	C/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802020	GTCTTCAACGAAGAA[C/G]TGGGCCCGTGTATTC	10482
rs368552636	snp	C/T	1.6855e-05	0.00290297	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800345	CCAGGGGGTGAAGGT[C/T]CCCAGGAGGGGAGAC	10482
rs368883684	snp	C/T	0.000148803	0.00862436	intron-variant	NXF1	GRCh38.p7	11:62801239	AGGAGGCACCACCAG[C/T]AAGTGGATCAGAGAC	10482
rs368988754	snp	A/G	0.000399281	0.0141238	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791778	CCAGAGGCTGCACCG[A/G]AACCGGGGGCCGGGA	10482
rs369066552	snp	A/G	3.29544e-05	0.00405908	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797378	TGGTGGGGGTAGCTC[A/G]TGGCCATCCTGTGGA	10482
rs369101376	snp	A/G	6.58892e-05	0.00573936	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797328	CCTACCTTGCAGGGC[A/G]GTAACGTCGTGGGGG	10482
rs369105346	snp	C/G/T	0.000131854	0.00811867	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792705	TCCTGAAGGCACCTG[C/G/T]AGTGGAAGAACAGGC	10482
rs369136240	snp	C/T	4.94189e-05	0.00497062	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792456	TTACAGGGGGGACTG[C/T]TTCTGAGGCATGACT	10482
rs369140445	snp	C/T	0.000153988	0.00877328	intron-variant	NXF1	GRCh38.p7	11:62801733	TCTAATTTGAGCCTG[C/T]CTCACCTTTAGCTGT	10482
rs369295052	snp	C/G/T	1.65263e-05	0.00287452	intron-variant	NXF1	GRCh38.p7	11:62796058	GTCAGGCGCAAGCAG[C/G/T]AGCTTACTGTCTGGG	10482
rs369302518	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801584	TGAACGGAGGCCTTT[A/G]AGGTCAAGGGCTTGT	10482
rs369336139	snp	A/G	0.000197687	0.00994004	upstream-variant-2KB, utr-variant-3-prime, synonymous-codon, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792674	CTGGGCAGATCTGGT[A/G]TAGTCCCAGTTGTTG	10482
rs369364496	snp	A/G/T	6.59885e-05	0.00574374	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803836	ACTCATTGCCACATC[A/G/T]CCATCATCTTCCTCA	10482
rs369478852	snp	A/G	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62798134	CTCCATCCAAAAAAA[A/G]AAAAAAAAAGGGCCT	10482
rs369512908	snp	A/T	1.6473e-05	0.00286988	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792548	CAGTAGAGGTAGGCC[A/T]ACCCTCGCCACTCAG	10482
rs369611028	snp	C/T	0.00398564	0.0444627	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805414	CGCCGGCAAACAACC[C/T]AACTCCCAAGCGCTC	10482
rs369663429	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805428	CTAACTCCCAAGCGC[C/T]CAGGACCGAAGTGTC	10482
rs369698968	in-del	-/C			upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792080	AGAGGGCCCGCCCCC[-/C]TCGCTCAGGGCTGGG	10482
rs369719710	snp	A/G	1.64895e-05	0.00287132	intron-variant	NXF1	GRCh38.p7	11:62795974	CATCAGGTACAATGT[A/G]CACTTCTCAGAGCCT	10482
rs369756097	snp	A/C/T	3.33997e-05	0.00408643	intron-variant	NXF1	GRCh38.p7	11:62803780	TTCAAACCAGACCAA[A/C/T]TGGTCACTCACTATC	10482
rs369778773	snp	C/G	3.29905e-05	0.0040613	intron-variant	NXF1	GRCh38.p7	11:62801291	CCTATCTAACACACC[C/G]TGCTTCCTCATGCCT	10482
rs369806410	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62796797	AAAATGGCTAGGTGC[A/G]GTGGCTCACGCCTCT	10482
rs369867420	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807105	ACAGGAAGGTGGGTA[A/G]GGGCATCATCTCCCT	10482
rs369873801	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62795347	TGGGCGTGGTAGTGC[A/G]CACCTGTAGTCCCAG	10482
rs370003937	snp	C/T	4.94205e-05	0.0049707	intron-variant	NXF1	GRCh38.p7	11:62801731	CATCTAATTTGAGCC[C/T]GCCTCACCTTTAGCT	10482
rs370034485	snp	C/T	0.000169986	0.00921759	intron-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791671	TGGGAAGCCAGCCCA[C/T]GTCTTACCGATGGCG	10482
rs370095023	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793298	TGTCCAGGATGGTCT[C/T]GATCTCTTGACCTCG	10482
rs370160484	snp	A/G	0.000126648	0.00795663	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800292	GGGCTGCACATCTCC[A/G]CAGACGGGCCCTGGT	10482
rs370306415	snp	C/G	0.000153988	0.00877328	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792719	GGAGTGGAAGAACAG[C/G]CAGCTCTGTAAGAAC	10482
rs370355994	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799190	AAGAAAAAGAGAAAG[A/G]ACTACAAGGCAAAAA	10482
rs370420810	snp	A/G	1.96342e-05	0.00313316	intron-variant	NXF1	GRCh38.p7	11:62796611	GGCTCTGTGGTCTAC[A/G]GCCATACAAGGACCC	10482
rs370486689	snp	A/G	5.16045e-05	0.00507933	synonymous-codon, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800337	TCAGCCTCCCAGGGG[A/G]TGAAGGTCCCCAGGA	10482
rs370510129	snp	A/T	1.64743e-05	0.00287	intron-variant	NXF1	GRCh38.p7	11:62801938	CCAGGCCCTTTAAAC[A/T]CACCCTTCGGTTCTC	10482
rs370685933	snp	C/T	0.000163987	0.00905353	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791859	ACAGCCCGAGGATGG[C/T]GAAGAAGCGGCCCCG	10482
rs370707760	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62803049	TTTTGGGCTGGGTGC[A/G]GTGGCTCATGCCTAT	10482
rs370794559	snp	C/G	1.65979e-05	0.00288074	intron-variant	NXF1	GRCh38.p7	11:62801430	AATCTTCAGGAAGCA[C/G]AAGGGAAGGAAAGGG	10482
rs370858949	snp	A/C/G/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805433	TCCCAAGCGCTCAGG[A/C/G/T]CCGAAGTGTCCCTAC	10482
rs370898387	snp	C/G	5.10669e-05	0.0050528	intron-variant	NXF1	GRCh38.p7	11:62805294	CCCACCCGCGCCCCA[C/G]ATAGCCAGTTCCCGA	10482
rs371065573	snp	A/C/G	0.000100613	0.00709212	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794209	CCCTCATTATTTACT[A/C/G]CTAGCCCTACTTCAG	10482
rs371080482	snp	G/T	3.3279e-05	0.00407902	intron-variant	NXF1	GRCh38.p7	11:62801448	GGGAAGGAAAGGGAA[G/T]ACTGAGAGGGTTTGC	10482
rs371276025	snp	C/G	0.00199481	0.0315187	intron-variant	NXF1	GRCh38.p7	11:62802887	GCCAAATGAAGACAT[C/G]CAGAGGAATTACTCC	10482
rs371315222	snp	A/G/T	0.000811576	0.0201288	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805403	GCTGGCCGCTACGCC[A/G/T]GCAAACAACCTAACT	10482
rs371322198	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62800669	GTGCCGTGGCATGAT[C/T]ATAGTTCACTGCAGC	10482
rs371322959	snp	A/G	3.30732e-05	0.00406638	intron-variant	NXF1	GRCh38.p7	11:62801244	GCACCACCAGCAAGT[A/G]GATCAGAGACGAATC	10482
rs371572466	snp	C/T	1.64827e-05	0.00287073	intron-variant	NXF1	GRCh38.p7	11:62798507	GAGTGAGAGATGCTG[C/T]GCTTGTTAGAATGAA	10482
rs371606823	snp	A/G	0.000153988	0.00877328	intron-variant	NXF1	GRCh38.p7	11:62801086	ATAGCCGAGCTATCA[A/G]TTCTCACTTCATTTC	10482
rs371695776	snp	A/G	3.29663e-05	0.00405981	intron-variant	NXF1	GRCh38.p7	11:62802061	ACTACAAGAGGAAAC[A/G]GGAGCATTACACTGG	10482
rs371714642	snp	A/C	0.000115694	0.00760484	intron-variant	NXF1	GRCh38.p7	11:62802166	AGCCAGCCACTCAGG[A/C]CTTGTCTTACCTCAA	10482
rs371721596	snp	G/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62805610	CCACGCCCCGCCCAA[G/T]ACCTGAACTTGCGGA	10482
rs371766905	snp	A/G	1.65836e-05	0.0028795	intron-variant	NXF1	GRCh38.p7	11:62795038	CAACAACACCTTAGG[A/G]TCACTAGTGCTTTAT	10482
rs371781263	snp	A/G	0.00786522	0.0622153	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791984	GGCCATCGCCTCCAA[A/G]GCGCCGCCATGGCCA	10482
rs371908085	snp	A/C/G	6.59156e-05	0.00574056	intron-variant	NXF1	GRCh38.p7	11:62797251	TCCCTGAAATCAAAC[A/C/G]GGTATTAGGAACATG	10482
rs372066032	snp	C/T			synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802246	TGCCTTGTCATACTT[C/T]CTGCCATAAGGAATC	10482
rs372087114	snp	A/C	0.000182188	0.00954258	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791963	AGCACGGCTAGCAGC[A/C]CCGTGGGCCATCGCC	10482
rs372102791	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794313	ATGCTTGCAACATTT[C/T]CTGCTGCTCTGGAGA	10482
rs372220381	snp	C/T	3.29777e-05	0.00406051	intron-variant	NXF1	GRCh38.p7	11:62795980	GTACAATGTACACTT[C/T]TCAGAGCCTGAGTGC	10482
rs372417047	snp	A/G	8.243e-05	0.00641936	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796075	GCTTACTGTCTGGGC[A/G]CTTATGTCTACCACG	10482
rs372428651	snp	A/G	1.64857e-05	0.00287099	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803867	AGGCGGGAAGACCGA[A/G]TACCAGAACCGCCTC	10482
rs372441369	snp	C/T	0.0006196	0.0175902	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791811	CGGCTGCCACAGCCA[C/T]GGAAGCCCAGAAGAC	10482
rs372515874	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806863	GCTGCCTAGGCCCTT[C/T]GACGCTCCCACCCAG	10482
rs372599517	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799639	GAGGGAGAGGCAGCG[C/T]CCCCGAGGGGGTCAG	10482
rs372713854	snp	C/G/T	0.0035852	0.042187	intron-variant	NXF1	GRCh38.p7	11:62796594	ACAAAAAAGAAAGTA[C/G/T]GGGCTCTGTGGTCTA	10482
rs372723035	snp	A/C	9.88338e-05	0.00702902	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792465	GGACTGCTTCTGAGG[A/C]ATGACTACGATCACT	10482
rs372752677	snp	A/G	0.000412062	0.0143479	intron-variant	NXF1	GRCh38.p7	11:62803586	TGCTGTGGGTAAGCA[A/G]AGAATAAAATGACCA	10482
rs372784460	snp	A/G	0.000131907	0.00812009	intron-variant	NXF1	GRCh38.p7	11:62795969	AGCAGCATCAGGTAC[A/G]ATGTACACTTCTCAG	10482
rs372816746	snp	A/C	4.49085e-05	0.00473838	intron-variant	NXF1	GRCh38.p7	11:62800513	GGAAGGAACAAAGGG[A/C]GGAGACCCTGGTGAA	10482
rs372818885	snp	A/G	1.68357e-05	0.00290131	intron-variant	NXF1	GRCh38.p7	11:62803756	CATATAATCTCATGA[A/G]CCACTAAATTCAAAC	10482
rs372842580	snp	A/G/T	0.000312989	0.012506	utr-variant-3-prime, missense, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797374	CAATTGGTGGGGGTA[A/G/T]CTCATGGCCATCCTG	10482
rs372883109	snp	G/T	0.000875616	0.0209055	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805418	GGCAAACAACCTAAC[G/T]CCCAAGCGCTCAGGA	10482
rs372916662	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804290	GACCTCTGAAAGCCA[C/T]CTGAAATCTGCCACT	10482
rs372967319	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797794	TGAAGAACTAAGAGA[C/G]AAGGGTCAGAAGTCA	10482
rs372996716	snp	A/G	3.29647e-05	0.00405971	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792704	GTCCTGAAGGCACCT[A/G]GAGTGGAAGAACAGG	10482
rs373307473	snp	C/G/T	0.000362704	0.013462	intron-variant	NXF1	GRCh38.p7	11:62795977	CAGGTACAATGTACA[C/G/T]TTCTCAGAGCCTGAG	10482
rs373437572	snp	G/T	4.94181e-05	0.00497057	intron-variant	NXF1	GRCh38.p7	11:62801649	AGAGGAAAAAGAAGG[G/T]TTTAGTGGTCACTGG	10482
rs373440750	snp	C/T	0.000122858	0.00783669	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791719	ACCGTAGCGCCAGAG[C/T]GCGGAGCGCAGGTCG	10482
rs373476244	snp	C/G	1.64754e-05	0.00287009	intron-variant	NXF1	GRCh38.p7	11:62801825	TGATAGATATCTGGA[C/G]GGAAGACACAGAGGG	10482
rs373510179	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797520	GCCTGGCTGGACAAC[A/G]TGGCAAAACCCATCT	10482
rs373571563	snp	A/G	0.000153988	0.00877328	intron-variant	NXF1	GRCh38.p7	11:62801443	CAGAAGGGAAGGAAA[A/G]GGAAGACTGAGAGGG	10482
rs373618263	snp	C/T	9.90949e-05	0.0070383	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801394	TGCGATTCAGGACAA[C/T]GTCAATGTTCTGGGC	10482
rs373725740	in-del	-/A			intron-variant	NXF1	GRCh38.p7	11:62798437	AACTCCGTCTCAAAT[-/A]AAAAAAAAAAAAAGA	10482
rs373873462	snp	A/T	8.24463e-05	0.00642	intron-variant	NXF1	GRCh38.p7	11:62797405	TGGAAAGGAAGTAAA[A/T]GTTGACAGTGTAGAC	10482
rs373921793	snp	C/G	4.94613e-05	0.00497275	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801331	CCAAAGGCCTTACCT[C/G]AGGGATGTTCTCTTC	10482
rs374083980	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807042	GAAAGAGGAAGAAAG[A/C]GGTCAATTGGGAAAA	10482
rs374112252	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794954	AATTGCTAGCAGGAA[C/T]AGCAATGAATGTCCG	10482
rs374156694	snp	A/G	9.93904e-05	0.00704878	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794250	TCCTACACATGCCCC[A/G]CACTCACTTCTGGGA	10482
rs374166859	snp	A/G	3.29473e-05	0.00405864	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802014	ACTGGCGTCTTCAAC[A/G]AAGAACTGGGCCCGT	10482
rs374187212	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62798191	CCAGCACTTTGGGAG[A/G]CCGAGGTAGGTGGAT	10482
rs374336402	snp	A/G	6.77932e-05	0.00582168	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805404	CTGGCCGCTACGCCG[A/G]CAAACAACCTAACTC	10482
rs374398347	snp	C/T	9.80056e-05	0.00699951	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791870	ATGGTGAAGAAGCGG[C/T]CCCGATCATGCTCAA	10482
rs374423285	snp	C/T	8.38638e-05	0.00647494	intron-variant	NXF1	GRCh38.p7	11:62797150	ATTCCCCCTCAACCT[C/T]GGGGTGGGGAGGGGG	10482
rs374463855	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793810	AACATGATGAAAGCC[C/T]GTCTCTACTAAAAAA	10482
rs374487764	snp	C/G/T	3.36158e-05	0.00409963	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792742	GTAAGAACTCTGACT[C/G/T]GTAAATGCCAGCTGA	10482
rs374496111	snp	A/C/T	8.23681e-05	0.00641702	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801955	ACCCTTCGGTTCTCC[A/C/T]GATCCAAAATCTTAT	10482
rs374649156	snp	C/T	1.64768e-05	0.00287021	intron-variant	NXF1	GRCh38.p7	11:62796273	CCCATATTTTGTTCG[C/T]ATCACACACTTACTA	10482
rs374730186	snp	C/G	1.64762e-05	0.00287016	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797375	AATTGGTGGGGGTAG[C/G]TCATGGCCATCCTGT	10482
rs374775963	snp	C/G	0.000593623	0.017218	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791937	GGGGCCGGCAGGTGA[C/G]CAGGGGCCGCAGCAC	10482
rs374951512	snp	C/T	4.94654e-05	0.00497295	intron-variant	NXF1	GRCh38.p7	11:62802073	AACAGGAGCATTACA[C/T]TGGGAGTCCAGAGCC	10482
rs375026902	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801172	ATCCAGCCTGTACAG[C/G]CTGTTGTTGCTCAAG	10482
rs375107993	snp	A/C/G	0.00985461	0.0695067	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791965	CACGGCTAGCAGCCC[A/C/G]GTGGGCCATCGCCTC	10482
rs375138728	snp	A/C			utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805416	CCGGCAAACAACCTA[A/C]CTCCCAAGCGCTCAG	10482
rs375317991	snp	C/G	1.64963e-05	0.00287192	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62795911	CTTACCTTCCTTGAA[C/G]ACTCCATTGACAGAA	10482
rs375341465	snp	C/T	0.00031568	0.0125595	intron-variant	NXF1	GRCh38.p7	11:62796023	ATTAAATGCCACCCC[C/T]ACCCCAATTCTAGGC	10482
rs375439808	snp	G/T	3.38558e-05	0.00411422	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800343	TCCCAGGGGGTGAAG[G/T]TCCCCAGGAGGGGAG	10482
rs375571103	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800848	AATCATAACTCACTG[C/G]AGCCTTGAACTCCTG	10482
rs375610299	in-del	-/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793844	AAAAAAAAAAAAAAA[-/T]ACAAAAATTAGCCAG	10482
rs375649985	snp	A/G	3.29506e-05	0.00405884	intron-variant	NXF1	GRCh38.p7	11:62801512	CTTTCCCTCCCTGAC[A/G]GATCCCACCTTATCA	10482
rs375715547	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62795337	AAAAATTAGCTGGGC[A/G]TGGTAGTGCGCACCT	10482
rs375722810	snp	C/T	1.70586e-05	0.00292045	intron-variant	NXF1	GRCh38.p7	11:62805290	GCCGCCCACCCGCGC[C/T]CCAGATAGCCAGTTC	10482
rs375723109	snp	A/G	9.88354e-05	0.00702908	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792448	AGGACTATTTACAGG[A/G]GGGACTGCTTCTGAG	10482
rs375895975	snp	C/T	1.64947e-05	0.00287177	intron-variant	NXF1	GRCh38.p7	11:62801287	ACTTCCTATCTAACA[C/T]ACCCTGCTTCCTCAT	10482
rs375954157	snp	A/G	1.83522e-05	0.00302915	intron-variant	NXF1	GRCh38.p7	11:62796596	AAAAAAGAAAGTATG[A/G]GCTCTGTGGTCTACA	10482
rs376131089	snp	A/G/T	0.000230732	0.0107388	intron-variant	NXF1	GRCh38.p7	11:62801869	AGGGAAGCCTAAGCC[A/G/T]CAAGAACAAGACCCA	10482
rs376232694	snp	G/T	1.67492e-05	0.00289384	intron-variant	NXF1	GRCh38.p7	11:62803774	ACTAAATTCAAACCA[G/T]ACCAACTGGTCACTC	10482
rs376313083	snp	A/G	1.64895e-05	0.00287132	intron-variant	NXF1	GRCh38.p7	11:62795972	AGCATCAGGTACAAT[A/G]TACACTTCTCAGAGC	10482
rs376343022	snp	C/G	0.000167986	0.00916323	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791766	GGACCTCCGCATCCA[C/G]AGGCTGCACCGGAAC	10482
rs376527046	snp	A/G	0.000461247	0.0151793	intron-variant	NXF1	GRCh38.p7	11:62797259	ATCAAACAGGTATTA[A/G]GAACATGGAAGCAGT	10482
rs376601184	snp	A/C			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807071	AATTGGTCCCTGGGG[A/C]TGCTTCCTCTCTTCA	10482
rs376611320	in-del	-/C	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62802591	TACAGGCATGTACTA[-/C]CATGCCCGGCTAATT	10482
rs376614748	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803543	TGCCAAGTATCACCC[C/T]GACGGTTAGGTCGGG	10482
rs376724883	snp	A/C/G	0.000118257	0.00768868	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805400	GGCGCTGGCCGCTAC[A/C/G]CCGGCAAACAACCTA	10482
rs376730888	snp	C/T	9.88761e-05	0.00703052	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798627	AGCCACCGTGCCTCC[C/T]GGGCTGCTCTAGGAG	10482
rs376985728	snp	A/G	0.000199601	0.00998802	intron-variant	NXF1	GRCh38.p7	11:62801447	AGGGAAGGAAAGGGA[A/G]GACTGAGAGGGTTTG	10482
rs377013242	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807334	GGGGGATCAGGGGCA[A/G]TGGTCATTCTTAGCA	10482
rs377023070	in-del	-/CA			intron-variant	NXF1	GRCh38.p7	11:62801634	GCTCATGATCAGCTA[-/CA]GAGGAAAAAGAAGGG	10482
rs377030288	snp	C/G	0.000153988	0.00877328	intron-variant	NXF1	GRCh38.p7	11:62797406	GGAAAGGAAGTAAAA[C/G]TTGACAGTGTAGACT	10482
rs377071396	snp	A/G	1.64852e-05	0.00287094	intron-variant	NXF1	GRCh38.p7	11:62803587	GCTGTGGGTAAGCAG[A/G]GAATAAAATGACCAC	10482
rs377282245	snp	A/G/T	1.6477e-05	0.00287024	intron-variant	NXF1	GRCh38.p7	11:62801693	GGGTGGGGGTGTGAG[A/G/T]AGTAGTAAGACTGGG	10482
rs377312684	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62805255	GGCCTCACGCCCCGG[A/G]GGCTGAGGCCTAGGC	10482
rs377325688	snp	A/G/T	1.64803e-05	0.00287052	splice-acceptor-variant	NXF1	GRCh38.p7	11:62796183	CCGGAACCGCAAGGC[A/G/T]GTGGGTAGAGGAGAA	10482
rs377353308	snp	A/G	1.64741e-05	0.00286998	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798600	ACGGGACAGAAGTGA[A/G]TGATGCTTCAGAGCC	10482
rs377438921	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62806954	AGCACATTTGGCAGA[C/T]TGAGTCACCAGCAGC	10482
rs377509078	snp	C/G	3.30344e-05	0.004064	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801395	GCGATTCAGGACAAC[C/G]TCAATGTTCTGGGCC	10482
rs377645345	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801375	GTAGCTGCCATACAG[A/C]TTCTGCGATTCAGGA	10482
rs377660358	snp	C/G	1.64746e-05	0.00287002	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792661	GATGAGTGAAGGCCT[C/G]GGCAGATCTGGTGTA	10482
rs377751596	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62794878	TCTACCCTCCAATTA[C/T]CACACTGTTGGCCAT	10482
rs527239479	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803636	CTCAAAGGCCTTCCT[A/G]CACTGTTAGTGGGAC	10482
rs527300714	snp	A/C	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62797098	ACAAAACAAAAAACA[A/C]AACAAAAAGATTGAT	10482
rs527364697	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803151	CAGTGAAACCCCGTC[C/T]CTACTAAAAATACAA	10482
rs527431440	snp	A/C	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62796744	CAAGACCAGCCTGGG[A/C]AACATGGCGAAACCC	10482
rs527451238	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797989	CACAAAGAAATTAGC[C/T]GGGCATTGTGGCACA	10482
rs527761622	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795432	AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG	10482
rs528059467	in-del	-/ACA	0.00119737	0.0244387	upstream-variant-2KB, cds-indel, nc-transcript-variant	TMEM223, NXF1	GRCh38.p7	11:62792131	CGCAGAACACGAAAT[-/ACA]ACATCACTCTTTATA	10482
rs528356473	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806699	AAGGAAGTTTCCACG[C/T]TAATGAAGTGTTGCA	10482
rs528429624	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805946	TGACTAATTAAGGGC[C/T]TTTTTTCCTCGAGGG	10482
rs528565976	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804994	AAATAGGGCATCAGG[A/G]CAGCCCACGAGCAGG	10482
rs528873016	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804989	GTAAAAAATAGGGCA[C/T]CAGGGCAGCCCACGA	10482
rs528898953	snp	C/T	9.89511e-05	0.00703319	intron-variant	NXF1	GRCh38.p7	11:62801298	AACACACCCTGCTTC[C/T]TCATGCCTAATACTG	10482
rs529155336	snp	C/G/T	0.000429571	0.0146494	intron-variant	NXF1	GRCh38.p7	11:62794930	GCGAAAAGCAGAATA[C/G/T]TTACCCTGAATTGCT	10482
rs529232773	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62795583	GCACCACTATGAGAC[A/G]GCTATTACTAACCCC	10482
rs529256089	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794113	TAGAGGCTACAGTGA[A/G]TTATGATCACCACTA	10482
rs529351154	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799912	AGGGTCCCTCTTGGC[C/G]CAAGGGCAAGAGGGG	10482
rs529390524	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793407	TTAAGCAGCCAAAAG[C/T]TTTGCCTTTTAAAAT	10482
rs529434632	snp	C/G	1.69758e-05	0.00291335	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800463	CAGCCCCTTTATCTT[C/G]TCCAATTCCCGCTCA	10482
rs529646755	snp	C/G	0.000399281	0.0141238	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791768	ACCTCCGCATCCAGA[C/G]GCTGCACCGGAACCG	10482
rs529776236	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797126	GATGTGTGCCTGGGT[C/G]TGCCCACCATTCCCC	10482
rs529795361	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797990	ACAAAGAAATTAGCC[A/G]GGCATTGTGGCACAT	10482
rs530402793	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793711	AAATTTGGCTGGGTG[C/T]AGTGCCTCATGCCTG	10482
rs530736105	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806765	GTCAGAGCCCAAAAT[A/T]GCCTGTGTCAGCAGT	10482
rs530957741	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805424	CAACCTAACTCCCAA[A/G]CGCTCAGGACCGAAG	10482
rs531091721	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798982	CCAGGTCTGGCTTTG[A/G]CCAAGACCCAAACAC	10482
rs531151039	snp	C/T	3.29451e-05	0.00405851	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792505	CCACTTCTGGGATCT[C/T]GCCCTTGGCCTGGAG	10482
rs531221594	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803116	ATGACGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	10482
rs531566515	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62795477	GTGACTCCATCTCAA[A/T]AAAAAGTAATAACTA	10482
rs531830903	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797831	AACGCATCATGAAAA[A/G]TATCCAGGGATCCAG	10482
rs532145780	snp	A/C	0.00114491	0.0238987	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791975	AGCCCCGTGGGCCAT[A/C]GCCTCCAAGGCGCCG	10482
rs532210838	snp	A/G	0.000235285	0.0108438	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791798	GGGGGCCGGGACACG[A/G]CTGCCACAGCCATGG	10482
rs532221867	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798462	AAAAGAAAAAGAAAA[A/G]GAAAAAGAAACCTAT	10482
rs532572341	in-del	-/AAAACA			intron-variant	NXF1	GRCh38.p7	11:62797097	AACAAAACAAAAAAC[-/AAAACA]AAAAGATTGATGTGT	10482
rs532688030	snp	C/T			utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796300	ACTAGGGTCTTTAAG[C/T]TTCTTCACATTTCTG	10482
rs532766834	snp	A/G	1.6649e-05	0.00288518	intron-variant	NXF1	GRCh38.p7	11:62803995	TAGAGTTAGAAACAG[A/G]AACACAAATTAGAAG	10482
rs532864812	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807404	CAGGCTCAGTGGCAG[C/T]ACTGGCCACTTGCCT	10482
rs532905673	snp	G/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804913	GAATATCCAGTTGAT[G/T]TGTAAGTCTCGAATA	10482
rs532917012	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805829	CCCTACCGGAATCTA[G/T]CCAGTGTTTCAGCTC	10482
rs533049195	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62800645	GTCTCACTCTGTCAC[C/T]CAAGTTCAGTGCCGT	10482
rs533249433	snp	C/T	0.448038	0.152581	intron-variant	NXF1	GRCh38.p7	11:62800605	CTTTTAAAATTTTTT[C/T]TTTTTTTTTTTTTTT	10482
rs533432313	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793294	ATGTTGTCCAGGATG[C/G]TCTTGATCTCTTGAC	10482
rs533588543	snp	C/G/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793203	CCTGCCTCAGCCTCC[C/G/T]GAGTAGTTGGGACTA	10482
rs533798568	snp	C/T	0.000115989	0.00761453	intron-variant	NXF1	GRCh38.p7	11:62796049	TAGGCTTCTGTCAGG[C/T]GCAAGCAGGAGCTTA	10482
rs533935303	in-del	-/GTAGTGCGCACCT	0.00676609	0.0577691	intron-variant	NXF1	GRCh38.p7	11:62795340	AATTAGCTGGGCGTG[-/GTAGTGCGCACCT]GTAGTCCCAGCTACT	10482
rs534145193	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795200	GTAATAACTACGGCC[A/G]GGCACAGTGTCTCAT	10482
rs534150757	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802539	TTTCCTAGGCTCAAG[C/T]GATCCTCCTGTCTCA	10482
rs534437979	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802866	CAAGCCCCACACTCA[A/G]CCTGAGCCAAATGAA	10482
rs534525938	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792090	CCCCCCTCGCTCAGG[A/G]CTGGGAGGAGACAAC	10482
rs534716752	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799468	GATTGTGGGGGTGAG[A/G]GTCCATGCCCCACCT	10482
rs534848767	snp	A/G	0.000157245	0.00886554	intron-variant	NXF1	GRCh38.p7	11:62804201	GGGCTTTTGAAAAAT[A/G]AAGTAGAAACTGGAA	10482
rs534973010	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796965	CCAGCTACTGGGGAG[A/G]CTGAGGCAGGAGAAT	10482
rs535022824	snp	C/T	4.95864e-05	0.00497903	intron-variant	NXF1	GRCh38.p7	11:62803371	CATCTCCACTCTCAG[C/T]GTGGCCTCCTATCTC	10482
rs535043933	snp	C/G/T	1.64741e-05	0.00286998	intron-variant	NXF1	GRCh38.p7	11:62801675	ACTGGGTTTGTGTGT[C/G/T]GGGGGTGGGGGTGTG	10482
rs535167524	snp	C/G			intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794587	TTATCCCCTCCCATG[C/G]AATCAATGTTTGGAA	10482
rs535384684	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800735	AGACTCCTGGGTAGC[C/T]AGGACTACAGGCATG	10482
rs535387824	snp	A/G	0.000100508	0.00708828	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791863	CCCGAGGATGGTGAA[A/G]AAGCGGCCCCGATCA	10482
rs535745564	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62806964	GCAGATTGAGTCACC[A/G]GCAGCCAATGTCAGG	10482
rs536114212	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804329	TGTCTATACAGTGCA[C/G]ACGCCAGTTACAAAT	10482
rs536278127	snp	C/T	0.000148254	0.00860844	intron-variant	NXF1	GRCh38.p7	11:62801734	CTAATTTGAGCCTGC[C/T]TCACCTTTAGCTGTT	10482
rs536462462	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796792	CAAAAAAAATGGCTA[A/G]GTGCGGTGGCTCACG	10482
rs536762233	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805622	CAAGACCTGAACTTG[C/T]GGAACCCCGGCTGGC	10482
rs536925627	in-del	-/A	0.187685	0.242109	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794165	CAAGAACTTGTCTCC[-/A]AAAAAAAAAACAAAA	10482
rs536935308	snp	A/T	0.0023933	0.0345097	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799210	CAAGGCAAAAAAGCA[A/T]CTAGAAAAATGAGGG	10482
rs536942138	snp	A/G/T	0.00159649	0.0282165	intron-variant	NXF1	GRCh38.p7	11:62802689	GTGATCCTCCACCTC[A/G/T]GCCTCTCAAAGTGCT	10482
rs536998167	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798193	AGCACTTTGGGAGGC[C/T]GAGGTAGGTGGATCA	10482
rs537076271	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798775	ATGGACTGCCTTGAA[A/G]GCTGTCTCTTTTCTC	10482
rs537116342	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806061	CCCCACCCCGCCCCG[C/T]CCTGAGTTGCTGAGT	10482
rs537179680	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805535	GCCGCCCGGAGAAAG[A/C]GCGGCCCCCTGCGCG	10482
rs537532606	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794563	TTAGCTATTGTTACC[G/T]TTTATCATTTATCCC	10482
rs537541448	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62797657	GTTGCAGTAAGCTAC[A/G]ATTGTGCCACTGCAC	10482
rs538004425	in-del	-/CCACTCAGCAACC	0.000872708	0.0208708	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792556	GTAGGCCTACCCTCG[-/CCACTCAGCAACC]CCACTCAGCTAACCT	10482
rs538049741	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807025	TCCCTGCCTCACATG[A/G]TGAAAGAGGAAGAAA	10482
rs538074197	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800806	ATTTTTTTGAGACAG[C/G]TTGCTCAGGCTAGAA	10482
rs538469793	snp	A/C	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798250	CTGGCGAACATGGTG[A/C]AACCCTGTCTCTACT	10482
rs538587372	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805149	CCCAACACCAGGATG[C/G]CAGCAGGAATCCAGG	10482
rs538676341	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799864	AACCTCAGCATGGAC[A/G]GCAACAGCCCTGGGC	10482
rs539009567	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795999	GAGCCTGAGTGCCCC[C/T]CCTTGCCTATTAAAT	10482
rs539325230	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62796903	GAAATCCCATCTGTA[C/T]GAAAAATACAAAAAT	10482
rs539461093	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792922	GAAGCTCAAGATAGT[C/T]TTTACAGTGGTAGGG	10482
rs539461357	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800187	CAAGTCAGAAGAGAA[A/G]AGAGAACATCTCAGG	10482
rs539531249	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798668	AAACCCGAGGGACAG[C/T]CCATCCCATCCTGCT	10482
rs539560251	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806794	GTGATACCTGGCAGA[A/G]CCATTAGCCCAACCC	10482
rs539596704	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792079	TAGAGGGCCCGCCCC[C/G]CTCGCTCAGGGCTGG	10482
rs539730010	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793856	AAATACAAAAATTAG[C/G]CAGGCATGGTGGTGT	10482
rs539792607	snp	A/C	3.29755e-05	0.00406038	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794283	ACTCGAGGTTCATGC[A/C]AGACTGGGTAGAGAA	10482
rs540138237	snp	C/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62803229	GAGACTGAGGCAGAA[C/T]AGCTTGAACCCGGGA	10482
rs540260053	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806670	CCCCTCTGGGATCCT[A/G]CTCCCCTGTGTGAAA	10482
rs540262052	snp	C/T	4.90208e-05	0.00495056	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800297	GCACATCTCCGCAGA[C/T]GGGCCCTGGTCAGGA	10482
rs540308714	snp	C/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793874	GGCATGGTGGTGTGT[C/G]CCTGTAATCCCAGCT	10482
rs540391457	snp	A/G	8.23649e-05	0.00641683	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802005	AGAGGCAGTACTGGC[A/G]TCTTCAACGAAGAAC	10482
rs540462343	snp	C/T	0.00279162	0.0372561	intron-variant	NXF1	GRCh38.p7	11:62795456	ACTCCAGCCTGGTGA[C/T]AGAGTGTGACTCCAT	10482
rs540519997	snp	A/C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800828	AGGCTAGAATGCAAC[A/C/G]GCACAATCATAACTC	10482
rs540801152	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804724	GGCCACTATGCTTCA[A/G]GCACTTGATAGGAAT	10482
rs540870744	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797026	TGAGCCAAGATCACA[C/T]CATTGCACTCCAGCC	10482
rs541310583	snp	A/C	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62798327	CAGCTACTTGGGCTC[A/C]GGAGGCTGAGGCAGG	10482
rs541937751	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793140	CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT	10482
rs542054822	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805770	GCACAAAGGGCTTCA[A/G]AGGAATGGAGACCGC	10482
rs542437358	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799317	AAACAAATCCTTGCT[A/G]TGGTGAGTGGGCACT	10482
rs542484594	snp	A/G	0.00159617	0.0282053	intron-variant	NXF1	GRCh38.p7	11:62797053	AGCCTGGGTGACACA[A/G]TGAGACACTGTCCAA	10482
rs542543509	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806417	CCTGGACGGTGGGTA[C/T]TCTGGGCAGGTGTCT	10482
rs542740512	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62796654	GAGTGAGTTGTGGCC[C/G]GGCATGGAAGCTCAT	10482
rs542756999	snp	A/G	4.00914e-05	0.00447706	intron-variant	NXF1	GRCh38.p7	11:62800492	CAGACTTCAACTGCA[A/G]AGGGTGGAAGGAACA	10482
rs542909607	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803003	AAAAGATAGATACTT[A/G]AGTGTGGAGTAATCA	10482
rs542941141	snp	C/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62795301	TCCAACATGGCGAAA[C/T]CCCTTCTCTACTAAA	10482
rs542973210	snp	A/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62800873	CTCCTGAGCTCAAGC[A/T]ATCCTCCCACCTCAG	10482
rs543014586	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798427	CGACGAGTGAAACTC[C/T]GTCTCAAATAAAAAA	10482
rs543034634	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794700	ATGAATATTGTTATA[C/T]GAATTTTCAGATGAG	10482
rs543077757	snp	A/G	0.000136286	0.00825376	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791968	GGCTAGCAGCCCCGT[A/G]GGCCATCGCCTCCAA	10482
rs543442611	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805248	CCCTAGCGGCCTCAC[A/G]CCCCGGGGGCTGAGG	10482
rs543689716	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792231	AAGTACACAAAGCAC[C/T]TAAGTCCTTCGGGTA	10482
rs544262647	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806532	CTTCCACTCCTGGAA[A/G]CAGGCAGAGCTTCTG	10482
rs544362479	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800265	TCTCAAAGGACAGGT[A/G]GTTCCAGCTCAGGGC	10482
rs544436563	snp	C/T			utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796169	GTGTGCTTCAGCAGC[C/T]GGAACCGCAAGGCTG	10482
rs544441345	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793230	ACTACAGGCGTGGAA[C/T]GCCAAGCCCCGCTAA	10482
rs544454467	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800915	AGCTTGGACTAGAGG[C/T]GTGCAAACTCCTAGC	10482
rs544502314	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799659	GAGGGGGTCAGTTCT[C/T]TGTCTCCTTGGTAGC	10482
rs544764837	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797704	GAGCCAGACCCTGTC[C/T]CAAAAAACAAAACAA	10482
rs544813567	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793985	CAGCCTGGGCAACAT[A/G]GCAAGACTCCACCTC	10482
rs544899954	snp	A/C	0.00835141	0.0640778	intron-variant	NXF1	GRCh38.p7	11:62797079	TCCAAAAAAAAAAAA[A/C]AAAACAAAACAAAAA	10482
rs545170043	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794771	AACCCAGACGGTACA[A/G]TTCCAGAGCCAAGCT	10482
rs545346596	snp	G/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795427	GTTGCAGTGAGCCAA[G/T]ATTGCGCCACTGCAC	10482
rs545500447	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793312	TTGATCTCTTGACCT[C/T]GTGATCTGGCCGCCT	10482
rs545517264	snp	C/T	6.59109e-05	0.0057403	intron-variant	NXF1	GRCh38.p7	11:62801868	TAGGGAAGCCTAAGC[C/T]GCAAGAACAAGACCC	10482
rs545775008	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792377	GGTCACAGTCACGGG[A/G]CGGCCTCGGGCCAGA	10482
rs545909622	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798828	GGAGCAGTACTCCAA[A/G]CCCAGGCTTTAAGCC	10482
rs546139081	in-del	-/AATAAT	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62803321	ACTCCATTTAAAAAA[-/AATAAT]AATAATAATTTTTGT	10482
rs546196648	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797109	AACAAAACAAAAAGA[C/T]TGATGTGTGCCTGGG	10482
rs546258116	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799743	CTGGCGGGGCCCCAG[C/G]TCTGGTCACATCTTG	10482
rs546262652	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806853	CTCTCCACTCGCTGC[C/G]TAGGCCCTTCGACGC	10482
rs546452092	snp	A/G	0.00279162	0.0372561	intron-variant	NXF1	GRCh38.p7	11:62798463	AAAGAAAAAGAAAAA[A/G]AAAAAGAAACCTATC	10482
rs546660451	snp	A/C	0.00199481	0.0315187	intron-variant	NXF1	GRCh38.p7	11:62800635	TTGGGACAGGGTCTC[A/C]CTCTGTCACCCAAGT	10482
rs546694940	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799071	AGGAGAGGCAAAGGA[A/G]TAAGAAAGGAAAAGG	10482
rs546919784	snp	A/G	1.64738e-05	0.00286995	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794337	CTGGAGAGAGGGTGG[A/G]CACCGGGCTGGAGGA	10482
rs546955969	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797108	AAACAAAACAAAAAG[A/G]TTGATGTGTGCCTGG	10482
rs547094061	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62796753	CCTGGGCAACATGGC[A/G]AAACCCTGTCTCTAC	10482
rs547256337	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800253	GCACGCGATCCTCTC[-/A]AAAGGACAGGTGGTT	10482
rs547688285	snp	A/G	0.00159617	0.0282053	intron-variant	NXF1	GRCh38.p7	11:62798155	AAAAGGGCCTGGTGC[A/G]AGTGGCTCACGTCTG	10482
rs547715030	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803175	AATACAAAAATTAGC[C/T]GGGCGTGGTGGTGGG	10482
rs547949135	snp	C/G	0.0023933	0.0345097	intron-variant	NXF1	GRCh38.p7	11:62802549	TCAAGCGATCCTCCT[C/G]TCTCAGCTTTCTGGA	10482
rs548025044	snp	A/G	0.000198436	0.00995884	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796552	TCGGTCTCCAGAGTC[A/G]TAAATTGCATAGTAC	10482
rs548046692	snp	C/T	0.000735889	0.0191678	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791700	CGCCGCAGCCGACGG[C/T]CAGACCGTAGCGCCA	10482
rs548332647	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798169	CGAGTGGCTCACGTC[C/T]GTAATCCCAGCACTT	10482
rs548450388	in-del	-/G			intron-variant	NXF1	GRCh38.p7	11:62797899	CTGGGAGGCCAAGGT[-/G]GATGGATTAGTTGAG	10482
rs548549264	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804206	TTTGAAAAATGAAGT[A/G]GAAACTGGAATTAGA	10482
rs548623502	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805417	CGGCAAACAACCTAA[C/G]TCCCAAGCGCTCAGG	10482
rs548686504	in-del	-/C	0.00279162	0.0372561	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806401	AAAGCACACTAATCT[-/C]CCTGGACGGTGGGTA	10482
rs548764089	snp	C/T	0.00826295	0.0637432	utr-variant-5-prime, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792014	AGCCGACTTCCGGGG[C/T]GGGGCTTCCTGCCGC	10482
rs548801990	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62798216	GTGGATCACCTGAGG[C/T]CAGGAATTCAAGGCC	10482
rs548866961	snp	C/T	3.29495e-05	0.00405877	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62798574	ATCGTTCGCGAATGG[C/T]GCTGTCAAGAACGGG	10482
rs548938607	snp	A/G	1.6525e-05	0.00287441	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801401	CAGGACAACGTCAAT[A/G]TTCTGGGCCACCAAA	10482
rs549008594	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795645	AATGTTACTTGTCCA[C/T]AGCCCCGCACAACCA	10482
rs549066793	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793437	TTTCAGGAGCCCAGG[C/T]ACAGTAACTCACACC	10482
rs549073375	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794150	AGCCTGGATGACAGC[A/G]CAAGAACTTGTCTCC	10482
rs549084120	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802107	GGGGAGGGGCATTAC[A/G]CTGGGAGTCCAGCTT	10482
rs549618184	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805071	ACAGGCATCAACCAC[C/T]CACAAAGTTCAAAGG	10482
rs549673617	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805830	CCTACCGGAATCTAG[C/T]CAGTGTTTCAGCTCG	10482
rs550521225	snp	A/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803898	TTCCAGACCTACGGT[A/T]TCCTTCACCATATTT	10482
rs550551027	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805425	AACCTAACTCCCAAG[A/C]GCTCAGGACCGAAGT	10482
rs550648674	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806767	CAGAGCCCAAAATAG[A/C]CTGTGTCAGCAGTGA	10482
rs550734104	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792045	AGAGCCGCCTTCCGC[C/T]CTCCCTGGGCGCCCC	10482
rs550766594	snp	C/T	0.00279162	0.0372561	intron-variant	NXF1	GRCh38.p7	11:62800594	TCTTTTCTAATCTTT[C/T]AAAATTTTTTCTTTT	10482
rs551069887	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802405	CTACTTGAGATACAC[A/G]TAGATTCTTTAACTC	10482
rs551518096	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806780	AGCCTGTGTCAGCAG[C/T]GATACCTGGCAGAGC	10482
rs551956128	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799805	CAGCTCATAGCACTG[C/G]GCAAGAGAGACAGAT	10482
rs551996360	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798685	CATCCCATCCTGCTC[A/G]TCCCTCCACTCCCTC	10482
rs552405608	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805942	ACGTTGACTAATTAA[A/G]GGCTTTTTTTCCTCG	10482
rs552447048	snp	C/T	0.000375446	0.0136961	utr-variant-5-prime, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792002	GCCGCCATGGCCAGC[C/T]GACTTCCGGGGTGGG	10482
rs552489783	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798482	AAGAAACCTATCCAG[A/G]AATCCTTGTGAGTGA	10482
rs552660195	snp	G/T	0.000217014	0.0104144	intron-variant	NXF1	GRCh38.p7	11:62804151	CCTCTCTGTGGGAGG[G/T]CAGCATCAGGGAAAA	10482
rs552979724	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806285	GCACCACCACCAGCC[A/C]CTGACTGTTGTCTCT	10482
rs553046456	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793859	TACAAAAATTAGCCA[A/G]GCATGGTGGTGTGTG	10482
rs553055880	snp	A/C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792084	GGCCCGCCCCCCTCG[A/C/T]TCAGGGCTGGGAGGA	10482
rs553185018	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802469	AGTAACAGGGCCTCA[C/T]TCTGTCACTCAGGCT	10482
rs553400268	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805744	CCCAGAACTCAGTGA[A/G]GAAGGGGGCCGCACA	10482
rs553738711	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795896	GGGACTCTAAAGATT[C/T]TTACCTTCCTTGAAG	10482
rs553920778	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802903	CAGAGGAATTACTCC[C/T]TCCCCCAACCAAAAT	10482
rs554059319	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794674	ATTCATCCTCACAAC[A/G]AACTTAGGAAATGAA	10482
rs554062771	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62802965	CCTGCTCTAAGGTGT[C/T]GGAAGATACTGATTC	10482
rs554318338	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798349	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	10482
rs554379977	snp	G/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62805226	CCGCTCCCCGCGGAC[G/T]CCGGGCCCCTAGCGG	10482
rs554476668	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799062	CTCAGGAAGAGGAGA[A/G]GCAAAGGAATAAGAA	10482
rs554820867	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806673	CTCTGGGATCCTGCT[C/T]CCCTGTGTGAAAGGA	10482
rs554861270	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798759	CCCGGGGCACCCAGA[C/T]ATGGACTGCCTTGAA	10482
rs554925478	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797576	CTGGGCATGGTGGTG[C/T]GTGCCTGGAGTCCTA	10482
rs555114295	snp	C/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62796981	CTGAGGCAGGAGAAT[C/T]ACTTGAACCCTGGGA	10482
rs555123272	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798902	TCACCTGTGCAGCCC[C/T]GGGAGGAGGGAATGG	10482
rs555182323	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800740	CCTGGGTAGCTAGGA[C/T]TACAGGCATGTGACA	10482
rs555452702	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793902	GCTACTCGGGAGGCT[A/G]AGATTGGAGAATTGC	10482
rs555518188	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806441	GGTGTCTCCATTCTC[A/T]GTGACTGGCTTTGAT	10482
rs555653833	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62806984	CCAATGTCAGGGGTT[C/G]TGCAGGCAGCTGAAG	10482
rs555725849	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62798348	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	10482
rs555797087	snp	C/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793413	AGCCAAAAGTTTTGC[C/G]TTTTAAAATTTCAGG	10482
rs555919775	snp	A/G	8.24015e-05	0.00641825	intron-variant	NXF1	GRCh38.p7	11:62803575	GGTATAGGGGTTGCT[A/G]TGGGTAAGCAGAGAA	10482
rs555974800	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800248	TGGGGAGCACGCGAT[C/T]CTCTCAAAGGACAGG	10482
rs556054526	snp	G/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62804419	TTTGTGAGGAGCTCT[G/T]CGTTTCCATGGCCAG	10482
rs556506823	snp	C/T	0.000312961	0.0125053	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801757	TAGCTGTTCTACTTG[C/T]TCTGGCTTCAGTTCA	10482
rs556724992	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792290	TTGGCTTCCTGGCAC[C/T]AGTGAGGCTCAATCT	10482
rs556958257	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800243	CAAAGTGGGGAGCAC[A/G]CGATCCTCTCAAAGG	10482
rs556977006	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805574	CTTAAGGCCGTCGTT[A/C/G]GAGGGGCGGGGCCTG	10482
rs556979005	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798794	GTCTCTTTTCTCTCT[A/G]CCTGACCCTGAGTGT	10482
rs557109978	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806160	CCTACTAGAAACCCA[A/T]CGTGTCAACGGGGCA	10482
rs557231568	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792854	ACATTAGTAAAAGTC[C/T]AGATGTTCTACCAAT	10482
rs557438127	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798220	ATCACCTGAGGTCAG[A/G]AATTCAAGGCCAGCC	10482
rs557494159	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62803272	AGTGAGCCGAGATCA[C/T]GCCACTGTACTCCAG	10482
rs557574120	snp	A/G/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62795134	GATTAAGTATATAAG[A/G/T]GTATAAGGGAAGCAC	10482
rs557670541	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62800827	CAGGCTAGAATGCAA[C/G]GGCACAATCATAACT	10482
rs558309870	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798282	AAAATACAAAAATTA[A/G]CCAGGTGTGGTAGCA	10482
rs558374927	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794578	TTTTATCATTTATCC[C/G]CTCCCATGGAATCAA	10482
rs558377617	snp	C/T	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62804583	GTCTTAAAAAAGGTC[C/T]CTAACTCCCAAAAGA	10482
rs558442929	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797769	AAAAAGGCTGGGTGC[A/G]TAAGTAGACTGAAGA	10482
rs558700363	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805161	ATGCCAGCAGGAATC[C/T]AGGAGTCAACAACTC	10482
rs559112607	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62802806	CCAAGATATTATTTA[C/T]ACCTTGCCTGCCCCT	10482
rs559444168	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798845	CCAGGCTTTAAGCCC[A/G]GGACCTCTTTCCCCT	10482
rs559444180	snp	A/C/G	0.00290633	0.0380166	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791993	CTCCAAGGCGCCGCC[A/C/G]TGGCCAGCCGACTTC	10482
rs559733393	snp	A/C	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62804962	CCGAGAGTTCAAGAC[A/C]GACTGGACGCAGTAA	10482
rs559827682	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62796716	ATGGGTGAATAGCTT[A/G]AGCCCAGGAGTTCAA	10482
rs559871343	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805407	GCCGCTACGCCGGCA[A/G]ACAACCTAACTCCCA	10482
rs559977047	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798474	AAAAGAAAAAGAAAC[C/T]TATCCAGGAATCCTT	10482
rs560260941	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807132	CCCTTTGCTGCCAAC[A/G]CTTCCTTTGGGAGAG	10482
rs560357007	snp	A/G	4.9552e-05	0.0049773	intron-variant	NXF1	GRCh38.p7	11:62801226	GAGAAGAGTTTAGAG[A/G]AGGCACCACCAGCAA	10482
rs560365419	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794094	ACAGCTTGTGCCCAG[A/G]AATTAGAGGCTACAG	10482
rs560376189	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795576	TCCTATAGCACCACT[A/G]TGAGACGGCTATTAC	10482
rs560534502	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62794011	ACCTCCAAAAAAAAA[A/T]AATAATAAAATAAAA	10482
rs560599506	snp	C/G	0.000111876	0.00747832	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791731	GAGCGCGGAGCGCAG[C/G]TCGAAGGGGCCACGA	10482
rs560761541	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803704	CATTTCTCACTCTAA[C/T]AGGTGGGAAAGGAAA	10482
rs560926452	snp	C/T	0.00318978	0.0398085	intron-variant	NXF1	GRCh38.p7	11:62797867	GCGCAGTGGCTCACA[C/T]CTGTAATCCCAGCAC	10482
rs561432628	snp	C/G	1.64746e-05	0.00287002	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792630	TTTGCCACTGTATTT[C/G]CAGACCTTACCTTGA	10482
rs561449943	in-del	-/AAAC			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793678	TGAGACCCTGTCTCA[-/AAAC]AAACAAGCAAATAAA	10482
rs561833180	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806741	TCCCCTGCCTAGAGG[C/G]AGCTGTGTGTCAGAG	10482
rs561968003	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807286	AGGCCTGAGGGTGGT[A/G/T]GGGGGAGGACAGGGT	10482
rs561984146	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805793	GAGACCGCGCCTCCA[C/G]GTGGGAGTGATGGCT	10482
rs562003805	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800124	GATTCTAGAAAAGGT[G/T]GTGTTCAGGAAGAAA	10482
rs562046063	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805421	AAACAACCTAACTCC[C/T]AAGCGCTCAGGACCG	10482
rs562128525	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799318	AACAAATCCTTGCTG[C/T]GGTGAGTGGGCACTT	10482
rs562139672	snp	A/T	1.69885e-05	0.00291444	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802255	ATACTTTCTGCCATA[A/T]GGAATCTAGAAATGA	10482
rs562204003	snp	A/G	8.23689e-05	0.00641698	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62798575	TCGTTCGCGAATGGC[A/G]CTGTCAAGAACGGGA	10482
rs562240561	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804347	GCCAGTTACAAATAT[A/G]ACCAGTTTAAGGATC	10482
rs562400875	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62803091	TTTGGGGGGCCAAGG[C/T]GGGCAGATCATGACG	10482
rs562427771	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798932	GGGTGGGAGCCCAGG[A/G]GCTCCGCTGCCTCAC	10482
rs562686599	snp	A/C	0.00199481	0.0315187	intron-variant	NXF1	GRCh38.p7	11:62797065	ACAGTGAGACACTGT[A/C]CAAAAAAAAAAAAAA	10482
rs562723765	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794735	CAGCCTACTTGCTAG[A/T]AGTGGTGGAGCCAGG	10482
rs562863380	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800881	CTCAAGCAATCCTCC[C/T]ACCTCAGCCCCCTGG	10482
rs562865836	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799835	TTGCATGCCACCAGC[C/T]CCTAGGAGGCCTCAA	10482
rs562958987	snp	A/G	4.43125e-05	0.00470683	intron-variant	NXF1	GRCh38.p7	11:62800510	GGTGGAAGGAACAAA[A/G]GGAGGAGACCCTGGT	10482
rs563004295	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797129	GTGTGCCTGGGTCTG[C/T]CCACCATTCCCCCTC	10482
rs563021098	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794193	AAAAAACTGTCAGGA[G/T]CCCTCATTATTTACT	10482
rs563194274	snp	C/G	0.00159617	0.0282053	intron-variant	NXF1	GRCh38.p7	11:62798023	CTGTAATCCCAGCTA[C/G]TCAGGAGGCTGAGGC	10482
rs563277133	snp	A/C/G	0.000214268	0.0103487	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791970	CTAGCAGCCCCGTGG[A/C/G]CCATCGCCTCCAAGG	10482
rs563315272	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805310	ATAGCCAGTTCCCGA[C/T]CCGAAGACCAGCACT	10482
rs563416668	snp	A/T	0.00438332	0.0466095	intron-variant	NXF1	GRCh38.p7	11:62798437	AACTCCGTCTCAAAT[A/T]AAAAAAAAAAAAAGA	10482
rs563936685	snp	A/C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805471	GCCACCGCATTTATA[A/C/T]AGCAAAGCACGTCGC	10482
rs563950731	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797140	TCTGCCCACCATTCC[C/T]CCTCAACCTCGGGGT	10482
rs563978252	snp	A/C	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62804899	TAGTGTTCAGACTAG[A/C]ATATCCAGTTGATGT	10482
rs564110522	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805890	CTATAAGATGGATTA[A/G]CAAATCACGAAGTTG	10482
rs564248160	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806570	TAGCTCAAGGAAGAA[C/T]TACGGCCAAATAGTT	10482
rs564264264	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62800916	GCTTGGACTAGAGGC[A/G]TGCAAACTCCTAGCC	10482
rs564338892	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807384	TTTCTCCCAAGTACC[C/T]TGCACAGGCTCAGTG	10482
rs564394280	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799752	CCCCAGCTCTGGTCA[C/T]ATCTTGGGGAACCCA	10482
rs564528629	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796681	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	10482
rs564792247	snp	A/C	0.00478085	0.0486577	intron-variant	NXF1	GRCh38.p7	11:62797083	AAAAAAAAAAAAAAA[A/C]CAAAACAAAAAACAA	10482
rs564818648	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793284	AGATTTCACCATGTT[A/G]TCCAGGATGGTCTTG	10482
rs565070658	snp	A/C	0.000399281	0.0141238	splice-donor-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791678	CCAGCCCACGTCTTA[A/C]CGATGGCGCCGCAGC	10482
rs565396102	snp	A/C	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795428	TTGCAGTGAGCCAAG[A/C]TTGCGCCACTGCACT	10482
rs565836824	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805943	CGTTGACTAATTAAG[A/G]GCTTTTTTTCCTCGA	10482
rs566164452	snp	A/G	0.000246305	0.0110947	intron-variant	NXF1	GRCh38.p7	11:62804162	GAGGGCAGCATCAGG[A/G]AAAAGTTACTGGAAA	10482
rs566343621	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62800690	TCACTGCAGCCTCAA[A/G]CTCCTGGACTCAAGA	10482
rs566489581	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62806923	GTCTTGCTGTAATTG[A/G]GAGAAAACGAGCTGC	10482
rs566587693	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792085	GCCCGCCCCCCTCGC[G/T]CAGGGCTGGGAGGAG	10482
rs566589381	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799123	GATGGGGCAGGGGCA[A/G]GGGAGAGATGGGGAG	10482
rs566596814	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800244	AAAGTGGGGAGCACG[C/T]GATCCTCTCAAAGGA	10482
rs566667813	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792421	CAGACGACAACCAGA[C/G]GGTAATATCCAAGGA	10482
rs566797529	snp	A/T	3.31818e-05	0.00407306	intron-variant	NXF1	GRCh38.p7	11:62794914	AGGACTGGTATCCAA[A/T]GCGAAAAGCAGAATA	10482
rs567315608	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796763	ATGGCGAAACCCTGT[C/G]TCTACTAAAAATACA	10482
rs567899202	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802680	CAGCCTCAAGTGATC[C/T]TCCACCTCGGCCTCT	10482
rs568155710	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805531	TGCCGCCGCCCGGAG[A/G]AAGCGCGGCCCCCTG	10482
rs568158252	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800035	AAGGCAACCCCATCT[A/G]TAGGGTATGTACAAG	10482
rs568246369	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797938	TTCAAGACCATCCTG[A/G]CCAACAAGATGAAAC	10482
rs568306177	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62795787	GGGGCAGAATGGGAG[A/G]AGGAGCTCAAAAAGA	10482
rs568376098	snp	A/G	0.00676609	0.0577691	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799186	AGCAAAGAAAAAGAG[A/G]AAGAACTACAAGGCA	10482
rs568408335	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805036	CATTAAAGGAAGAGT[C/G]AGGCCGCCAAACCTA	10482
rs568642806	snp	A/C	1.64754e-05	0.00287009	intron-variant	NXF1	GRCh38.p7	11:62801521	CCTGACAGATCCCAC[A/C]TTATCACCACCTATC	10482
rs568755149	snp	C/T	1.65029e-05	0.00287248	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794945	CTTACCCTGAATTGC[C/T]AGCAGGAACAGCAAT	10482
rs568790996	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792027	GGTGGGGCTTCCTGC[C/T]GCAGAGCCGCCTTCC	10482
rs568964190	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794543	ACAAGGTCCCCCTCC[C/T]ACTCTTAGCTATTGT	10482
rs569090725	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62795660	CAGCCCCGCACAACC[A/G]AAACTAGGATGGAAA	10482
rs569196618	in-del	-/T	0.0119828	0.076471	intron-variant	NXF1	GRCh38.p7	11:62800605	TTTTAAAATTTTTTC[-/T]TTTTTTTTTTTTTTT	10482
rs569346967	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62794841	TTCCTGTTGCCTTTC[C/T]GAAATCACCCCAAAG	10482
rs569454618	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62798445	CTCAAATAAAAAAAA[A/G]AAAAAGAAAAAGAAA	10482
rs569611190	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62805144	GGTCCCCCAACACCA[A/G]GATGCCAGCAGGAAT	10482
rs570285180	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62796850	GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGTTGG	10482
rs570422698	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62806204	ACCAGCAGTGGCAAC[C/T]TGCTGGAGATGCCGA	10482
rs570578300	snp	A/C	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62798239	TCAAGGCCAGCCTGG[A/C]GAACATGGTGAAACC	10482
rs570641248	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798646	CTGCTCTAGGAGCAA[A/G]TATACCAAACCCGAG	10482
rs570724715	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800185	GTCAAGTCAGAAGAG[A/G]AGAGAGAACATCTCA	10482
rs570751528	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793780	CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	10482
rs570788087	snp	A/G	0.00119737	0.0244387	intron-variant	NXF1	GRCh38.p7	11:62800597	TTTCTAATCTTTTAA[A/G]ATTTTTTCTTTTTTT	10482
rs570816037	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792074	CCCGCTAGAGGGCCC[C/G]CCCCCCTCGCTCAGG	10482
rs570879003	in-del	-/C	0.00279162	0.0372561	intron-variant	NXF1	GRCh38.p7	11:62800605	CTTTTAAAATTTTTT[-/C]TTTTTTTTTTTTTTT	10482
rs570974163	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802451	CACTTACTATTTTTT[C/T]TTAGTAACAGGGCCT	10482
rs571013295	snp	A/C/G	3.29453e-05	0.00405854	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792544	AGGTCAGTAGAGGTA[A/C/G]GCCTACCCTCGCCAC	10482
rs571037374	snp	A/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795816	GAAAATGGGAGAGAA[A/G]GTAGCTGGGAAGCTA	10482
rs571292392	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799245	AAGGGAGAAAGACAC[C/G]CTGACACAGCCCTTT	10482
rs571891974	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800157	GAAAGGCCACAGACC[C/T]AGCAAACAGATAGTC	10482
rs571908829	snp	A/G	0.000182874	0.00956052	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791946	AGGTGAGCAGGGGCC[A/G]CAGCACGGCTAGCAG	10482
rs572043513	snp	A/G	0.000416753	0.0144292	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791684	CACGTCTTACCGATG[A/G]CGCCGCAGCCGACGG	10482
rs572173005	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805196	GTCCACCTCGAGTGC[C/T]CGGCCCCCCGCGCGC	10482
rs572447497	snp	A/G/T	3.29458e-05	0.00405857	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792474	CTGAGGCATGACTAC[A/G/T]ATCACTTCATGAATG	10482
rs572609032	snp	C/T	1.64779e-05	0.00287031	intron-variant	NXF1	GRCh38.p7	11:62796258	TTCCCATGCCCTTTT[C/T]CCATATTTTGTTCGT	10482
rs572823445	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799285	GCCCCATCCCTGTGG[G/T]CCAAGGTAGAAATGA	10482
rs573010773	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792953	AAAGATGTTCATGGT[A/G/T]TAAGTAAAGAAACTA	10482
rs573340299	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805755	GTGAGGAAGGGGGCC[G/T]CACAAAGGGCTTCAG	10482
rs573960061	snp	G/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62800871	AACTCCTGAGCTCAA[G/T]CAATCCTCCCACCTC	10482
rs573995007	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62796608	ATGGGCTCTGTGGTC[C/T]ACAGCCATACAAGGA	10482
rs573996984	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807135	TTTGCTGCCAACGCT[C/T]CCTTTGGGAGAGGCT	10482
rs574028053	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62795296	TCCTGTCCAACATGG[C/T]GAAACCCCTTCTCTA	10482
rs574247208	snp	C/G	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62801677	TGGGTTTGTGTGTGG[C/G]GGGTGGGGGTGTGAG	10482
rs574379503	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62798412	GCACTCCAGCCTGGG[C/T]GACGAGTGAAACTCC	10482
rs574442552	snp	C/T	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62805247	CCCCTAGCGGCCTCA[C/T]GCCCCGGGGGCTGAG	10482
rs574614677	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798767	ACCCAGACATGGACT[A/G]CCTTGAAGGCTGTCT	10482
rs574675649	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	TMEM223, NXF1	GRCh38.p7	11:62792194	CACTCTTTATATTAA[A/G]AAGTAAGGAGGTCCT	10482
rs574986777	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798955	TGCCTCACCAGGTAT[C/G]CATCAGTTCTGCCAG	10482
rs575300975	snp	A/G	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62805213	GGCCCCCCGCGCGCC[A/G]CTCCCCGCGGACGCC	10482
rs575447028	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793488	AGGCCTAGGTGGGCA[A/G]CATGGTGAAACCCCA	10482
rs575754059	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800261	ATCCTCTCAAAGGAC[A/C]GGTGGTTCCAGCTCA	10482
rs575800499	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793226	TGGGACTACAGGCGT[A/G]GAACGCCAAGCCCCG	10482
rs575934421	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799403	GAAGCAAAGCAGCCA[G/T]GGGGGCAGGAGACCT	10482
rs576299482	snp	A/C	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62797077	TGTCCAAAAAAAAAA[A/C]AAAAAACAAAACAAA	10482
rs576455150	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799851	CCTAGGAGGCCTCAA[C/T]CTCAGCATGGACAGC	10482
rs576509953	snp	C/G	0.000399281	0.0141238	intron-variant	NXF1	GRCh38.p7	11:62802706	CCTCTCAAAGTGCTG[C/G]GATTACAGGCATGAG	10482
rs576518236	snp	G/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62803336	AATAATAATAATAAT[G/T]TTTGTGGAATAAAAT	10482
rs576584213	snp	C/T	0.000798403	0.0199641	intron-variant	NXF1	GRCh38.p7	11:62800903	GCCCCCTGGGGCAGC[C/T]TGGACTAGAGGCGTG	10482
rs576775090	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792362	AGCCCTCCCTCCCTC[A/G]GTCACAGTCACGGGG	10482
rs576909666	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799239	GGAGAAAAGGGAGAA[A/G]GACACCCTGACACAG	10482
rs576914356	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793278	GAGACGAGATTTCAC[C/T]ATGTTGTCCAGGATG	10482
rs576937090	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NXF1	GRCh38.p7	11:62805596	CGGGGCCTGGCCCTC[C/T]ACGCCCCGCCCAAGA	10482
rs577052659	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798797	TCTTTTCTCTCTGCC[C/T]GACCCTGAGTGTCAA	10482
rs577296351	snp	A/G/T	7.84506e-05	0.00626261	synonymous-codon, missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791928	TGCCTTGCAGGGGCC[A/G/T]GCAGGTGAGCAGGGG	10482
rs577595642	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799733	CCCTCGCCTGCTGGC[A/G]GGGCCCCAGCTCTGG	10482
rs577923186	snp	C/T	0.000296511	0.0121724	intron-variant	NXF1	GRCh38.p7	11:62801924	CACCTCCAGCCAAGC[C/T]AGGCCCTTTAAACAC	10482
rs577955921	snp	A/T	0.0150606	0.0854603	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62794014	TCCAAAAAAAAAAAA[A/T]AATAAAATAAAATAA	10482
rs745404912	snp	A/C	1.65537e-05	0.0028769	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801416	GTTCTGGGCCACCAA[A/C]TCTTCAGGAAGCAGA	10482
rs745414922	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62803613	ACCACAAATGCTAGG[A/C]AAGTCTTCTCAAAGG	10482
rs745432969	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799620	TGACGTGCAGTGTGT[A/G]AGTGAGGGAGAGGCA	10482
rs745472928	snp	A/G	6.32731e-05	0.00562428	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791823	CCATGGAAGCCCAGA[A/G]GACGCCCTGGCCCGC	10482
rs745492057	snp	A/G	4.97409e-05	0.00498678	stop-gained, nc-transcript-variant	NXF1	GRCh38.p7	11:62803796	TGGTCACTCACTATC[A/G]TACTCGGGGACCATC	10482
rs745558995	snp	A/G	3.2975e-05	0.00406035	intron-variant	NXF1	GRCh38.p7	11:62801320	CTAATACTGGGCCAA[A/G]GGCCTTACCTCAGGG	10482
rs745574134	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803878	CCGAATACCAGAACC[A/G]CCTCTTCCAGACCTA	10482
rs745578842	snp	C/T	0.000200969	0.0100222	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791900	AAGAGCAGCACATCC[C/T]GTTGCAGCGTCGTGC	10482
rs745675525	snp	A/C	2.63342e-05	0.00362855	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800280	GGTTCCAGCTCAGGG[A/C]TGCACATCTCCGCAG	10482
rs745744970	snp	C/G	3.29511e-05	0.00405887	intron-variant	NXF1	GRCh38.p7	11:62801823	GATGATAGATATCTG[C/G]AGGGAAGACACAGAG	10482
rs745754466	snp	G/T	4.00184e-05	0.00447299	intron-variant	NXF1	GRCh38.p7	11:62804059	AGCTTCTAGTACTCT[G/T]AACTATTGGAAGAGA	10482
rs745766457	snp	G/T	1.64727e-05	0.00286986	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792495	TTCATGAATGCCACT[G/T]CTGGGATCTCGCCCT	10482
rs745902414	snp	A/G	3.29473e-05	0.00405864	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792436	CGGTAATATCCAAGG[A/G]CTATTTACAGGGGGG	10482
rs745911085	in-del	-/C	4.94181e-05	0.00497057	intron-variant	NXF1	GRCh38.p7	11:62797301	ACACAAGTTCTTACT[-/C]TGTCCATGCTTCCTA	10482
rs745912517	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62794775	CAGACGGTACAATTC[C/T]AGAGCCAAGCTATTA	10482
rs745978586	snp	A/G	1.64741e-05	0.00286998	intron-variant	NXF1	GRCh38.p7	11:62801706	AGAAGTAGTAAGACT[A/G]GGTTGGAAACATCTA	10482
rs746034281	snp	C/T	3.29527e-05	0.00405898	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796153	AACAACGTTGAGACG[C/T]GTGTGCTTCAGCAGC	10482
rs746161774	snp	C/T	1.6477e-05	0.00287024	intron-variant	NXF1	GRCh38.p7	11:62796262	CATGCCCTTTTCCCA[C/T]ATTTTGTTCGTATCA	10482
rs746208203	snp	C/T	0.000371816	0.0136297	intron-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791647	TCCCGCCACCCCACG[C/T]TGTCACAGTGGGAAG	10482
rs746268487	snp	A/G	4.3482e-05	0.00466252	intron-variant	NXF1	GRCh38.p7	11:62800507	AAGGGTGGAAGGAAC[A/G]AAGGGAGGAGACCCT	10482
rs746277226	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803514	GCACAGTAACATGAA[C/T]GCGATCTCGATCATG	10482
rs746413007	snp	A/G	1.98238e-05	0.00314825	intron-variant	NXF1	GRCh38.p7	11:62802306	ATGATAAGTAAGGCT[A/G]AATAGCAGACCCAAT	10482
rs746550849	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797693	CCTGGATGACAGAGC[C/T]AGACCCTGTCTCAAA	10482
rs746589453	snp	A/G	1.64743e-05	0.00287	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62798550	TTACCAGGCGTAGTA[A/G]CTTGGGAAATCGTTC	10482
rs746642105	in-del	-/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800211	TCTCAGGACAAAGCT[-/G]GAAGACACAGACAGA	10482
rs746714258	snp	C/T	3.31686e-05	0.00407225	intron-variant	NXF1	GRCh38.p7	11:62794916	GACTGGTATCCAATG[C/T]GAAAAGCAGAATACT	10482
rs746717028	snp	G/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803558	CGACGGTTAGGTCGG[G/T]TGGTATAGGGGTTGC	10482
rs746801609	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801801	GGGGTGGAGCAGAAG[A/G]GTTGATGATGATAGA	10482
rs746822446	snp	C/G	1.64749e-05	0.00287005	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797369	AAAGGCAATTGGTGG[C/G]GGTAGCTCATGGCCA	10482
rs746903242	snp	A/C	1.77461e-05	0.00297871	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791986	CCATCGCCTCCAAGG[A/C]GCCGCCATGGCCAGC	10482
rs746921131	snp	C/T	3.29582e-05	0.00405931	intron-variant	NXF1	GRCh38.p7	11:62796252	GATTCCTTCCCATGC[C/T]CTTTTCCCATATTTT	10482
rs747003486	snp	A/G	1.64735e-05	0.00286993	intron-variant	NXF1	GRCh38.p7	11:62801690	GGGGGGTGGGGGTGT[A/G]AGAAGTAGTAAGACT	10482
rs747060941	snp	C/G	1.88699e-05	0.00307158	intron-variant	NXF1	GRCh38.p7	11:62804055	TCATAGCTTCTAGTA[C/G]TCTGAACTATTGGAA	10482
rs747068098	snp	G/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806599	TTGGAGGATACAGAT[G/T]AAACAGGTCCAAACA	10482
rs747170041	snp	A/G	1.84405e-05	0.00303643	intron-variant	NXF1	GRCh38.p7	11:62802289	AAAGAGAAAAGAAGG[A/G]AATGATAAGTAAGGC	10482
rs747181425	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792894	AAGATAAGGAATATT[A/G]AATAGCTGTCAAGAA	10482
rs747186468	in-del	-/CCCTACTTC	8.37809e-05	0.00647174	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794213	ATTATTTACTACTAG[-/CCCTACTTC]CCCTACTTCAGTGCA	10482
rs747190810	snp	C/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62805650	GGCAGCCAGCATGTC[C/T]CCGCACCTTTTCATC	10482
rs747195580	snp	C/T	1.6501e-05	0.00287232	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800426	ACAGGGAGTTTCCAT[C/T]GAGCCAGAGCTCTTC	10482
rs747257497	snp	A/G	2.03308e-05	0.00318826	intron-variant	NXF1	GRCh38.p7	11:62800496	CTTCAACTGCAAAGG[A/G]TGGAAGGAACAAAGG	10482
rs747322028	snp	C/T	1.66136e-05	0.00288211	intron-variant	NXF1	GRCh38.p7	11:62796027	AATGCCACCCCCACC[C/T]CAATTCTAGGCTTCT	10482
rs747356441	snp	A/G	6.87474e-05	0.00586251	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792813	TGTACATTCTTATAC[A/G]TCCTTGCACTATTTA	10482
rs747371455	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799384	CGATCTGAACTGGGC[A/G]TGGGAAGCAAAGCAG	10482
rs747409349	snp	C/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62806934	ATTGGGAGAAAACGA[C/G]CTGCAGCACATTTGG	10482
rs747427218	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62798030	CCCAGCTACTCAGGA[A/G]GCTGAGGCAGGAGAA	10482
rs747511104	snp	A/C	1.68935e-05	0.00290628	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805398	CAGGCGCTGGCCGCT[A/C]CGCCGGCAAACAACC	10482
rs747524916	snp	A/C	4.99073e-05	0.00499511	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792734	GCAGCTCTGTAAGAA[A/C]TCTGACTCGTAAATG	10482
rs747566315	snp	G/T	1.69945e-05	0.00291496	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807466	CCTCAGAGTAGAGAG[G/T]GTTCAAGCAAGGAAG	10482
rs747569578	snp	A/G	1.64768e-05	0.00287021	intron-variant	NXF1	GRCh38.p7	11:62797260	TCAAACAGGTATTAG[A/G]AACATGGAAGCAGTA	10482
rs747699226	snp	A/G	1.65184e-05	0.00287384	intron-variant	NXF1	GRCh38.p7	11:62803374	CTCCACTCTCAGCGT[A/G]GCCTCCTATCTCTAC	10482
rs747725374	in-del	-/C			intron-variant	NXF1	GRCh38.p7	11:62802471	TAACAGGGCCTCACT[-/C]TGTCACTCAGGCTGG	10482
rs747747714	snp	C/T	1.64746e-05	0.00287002	intron-variant	NXF1	GRCh38.p7	11:62797280	TGGAAGCAGTATTCT[C/T]TCCACACACAAGTTC	10482
rs747785420	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802893	TGAAGACATCCAGAG[A/G]AATTACTCCCTCCCC	10482
rs747870705	in-del	-/G	3.30628e-05	0.00406575	intron-variant	NXF1	GRCh38.p7	11:62801244	GCACCACCAGCAAGT[-/G]GATCAGAGACGAATC	10482
rs747898852	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62801532	CCACCTTATCACCAC[A/C]TATCTGAGAACTACT	10482
rs747916725	snp	C/T	9.16884e-05	0.00677022	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791978	CCCGTGGGCCATCGC[C/T]TCCAAGGCGCCGCCA	10482
rs747925585	in-del	-/C	1.68018e-05	0.00289838	frameshift-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62805342	ACCGCTGTACGACTT[-/C]CCCTCGTCCGCCATG	10482
rs747928914	snp	A/G	0.000108044	0.00734917	intron-variant	NXF1	GRCh38.p7	11:62804150	CCCTCTCTGTGGGAG[A/G]GCAGCATCAGGGAAA	10482
rs748011157	snp	C/G	3.3106e-05	0.0040684	intron-variant	NXF1	GRCh38.p7	11:62795995	CTCAGAGCCTGAGTG[C/G]CCCCCCTTGCCTATT	10482
rs748168123	snp	A/G	1.6736e-05	0.0028927	intron-variant	NXF1	GRCh38.p7	11:62804025	GTAAGTAACTGGTCC[A/G]GTTTGGTGTGGCAAT	10482
rs748175873	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793926	GAATTGCTTGAACCC[A/G]GGAGGCAGAGGTTAC	10482
rs748197436	snp	C/T	1.64879e-05	0.00287118	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800398	TAGGTGGACTGGTCT[C/T]GGAAGGTGTCACACA	10482
rs748327258	snp	C/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62805569	GCACACTTAAGGCCG[C/T]CGTTCGAGGGGCGGG	10482
rs748356744	snp	A/G	0.000149245	0.00863714	intron-variant	NXF1	GRCh38.p7	11:62802134	GCTTGCCCCTTCACC[A/G]TCCCTGGTGCCTGGC	10482
rs748363664	snp	C/T	1.72734e-05	0.00293878	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807453	CCCCAACAGAGTGCC[C/T]CAGAGTAGAGAGGGT	10482
rs748390879	snp	C/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802003	GCAGAGGCAGTACTG[C/G]CGTCTTCAACGAAGA	10482
rs748430818	snp	C/T	1.64732e-05	0.0028699	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792542	GAAGGTCAGTAGAGG[C/T]AGGCCTACCCTCGCC	10482
rs748444083	snp	A/C	2.00914e-05	0.00316943	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800316	CCCTGGTCAGGATGC[A/C]TTAGCTCAGCCTCCC	10482
rs748502449	snp	C/T	0.000131789	0.00811648	intron-variant	NXF1	GRCh38.p7	11:62796432	GAAACCCAGTGGTCC[C/T]GGGCAGATTCTGGGA	10482
rs748513110	in-del	-/C	1.64738e-05	0.00286995	intron-variant	NXF1	GRCh38.p7	11:62801546	CCTATCTGAGAACTA[-/C]TGCTGTCAACCATAC	10482
rs748523339	snp	A/G	1.67649e-05	0.0028952	intron-variant	NXF1	GRCh38.p7	11:62797146	CACCATTCCCCCTCA[A/G]CCTCGGGGTGGGGAG	10482
rs748531250	snp	G/T	3.37935e-05	0.00411043	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805395	GCTCAGGCGCTGGCC[G/T]CTACGCCGGCAAACA	10482
rs748567437	snp	C/G	0.000127159	0.00797266	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791889	GATCATGCTCAAAGA[C/G]CAGCACATCCCGTTG	10482
rs748590666	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797819	AAGTCAAGTGTAAAC[A/G]CATCATGAAAAGTAT	10482
rs748593573	snp	C/T	1.64893e-05	0.0028713	intron-variant	NXF1	GRCh38.p7	11:62801309	CTTCCTCATGCCTAA[C/T]ACTGGGCCAAAGGCC	10482
rs748667827	snp	C/T	1.64754e-05	0.00287009	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796534	GGCATCCAGGAGCCC[C/T]TGTCGGTCTCCAGAG	10482
rs748767157	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62801281	CCAGCCACTTCCTAT[C/T]TAACACACCCTGCTT	10482
rs748856620	snp	A/G	1.64765e-05	0.00287019	intron-variant	NXF1	GRCh38.p7	11:62797267	GGTATTAGGAACATG[A/G]AAGCAGTATTCTCTC	10482
rs748880454	snp	C/G	1.66338e-05	0.00288386	intron-variant	NXF1	GRCh38.p7	11:62801433	CTTCAGGAAGCAGAA[C/G]GGAAGGAAAGGGAAG	10482
rs748888134	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799999	GGCTTCCTCAACCCA[C/T]GGACACCAGGCTCTT	10482
rs748935529	snp	G/T	1.66832e-05	0.00288814	intron-variant	NXF1	GRCh38.p7	11:62797161	ACCTCGGGGTGGGGA[G/T]GGGGGACCCTGGGAT	10482
rs748937906	snp	A/C	1.66829e-05	0.00288811	intron-variant	NXF1	GRCh38.p7	11:62804009	GGAACACAAATTAGA[A/C]GTAAGTAACTGGTCC	10482
rs748952021	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804346	CGCCAGTTACAAATA[C/T]GACCAGTTTAAGGAT	10482
rs749002783	in-del	-/TAA	0.000131993	0.00812274	intron-variant	NXF1	GRCh38.p7	11:62795888	ACAAACTCGGGACTC[-/TAA]AGATTCTTACCTTCC	10482
rs749010208	snp	A/C	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62801557	ACTACTGCTGTCAAC[A/C]ATACCTGGGTCTGAA	10482
rs749060470	snp	C/G			missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791842	GCCCTGGCCCGCGCA[C/G]AACAGCCCGAGGATG	10482
rs749073202	in-del	-/TG			intron-variant	NXF1	GRCh38.p7	11:62804136	CCACAGGAAAGAACC[-/TG]CTCTCTGTGGGAGGG	10482
rs749077066	snp	A/G	3.96393e-05	0.00445175	stop-gained, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791904	GCAGCACATCCCGTT[A/G]CAGCGTCGTGCCTTG	10482
rs749100377	snp	A/G	1.64814e-05	0.00287061	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803895	CTCTTCCAGACCTAC[A/G]GTTTCCTTCACCATA	10482
rs749111650	in-del	-/CGG			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793146	GCAGTGGCGTGATCT[-/CGG]CGGCTCACTGCAACC	10482
rs749130606	snp	G/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806364	CCTCAGAATGTGGTT[G/T]TGAGTCTCGGTCAGG	10482
rs749185954	in-del	-/T	4.94214e-05	0.00497074	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798596	AGAACGGGACAGAAG[-/T]TGAGTGATGCTTCAG	10482
rs749236587	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62796364	GGGGAATAAAAGGAA[C/T]GGACGTGGTGTTCAG	10482
rs749291485	snp	A/G	1.64977e-05	0.00287203	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800382	TACAACTGACCTGAT[A/G]TAGGTGGACTGGTCT	10482
rs749315333	snp	C/T	3.29984e-05	0.00406179	intron-variant	NXF1	GRCh38.p7	11:62795885	GCTACAAACTCGGGA[C/T]TCTAAAGATTCTTAC	10482
rs749454348	snp	C/T	6.58913e-05	0.00573945	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796499	GGAATGCTCAGGGAA[C/T]AGCAGGCCCCATCAT	10482
rs749462262	snp	A/C/G	3.2948e-05	0.00405871	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792447	AAGGACTATTTACAG[A/C/G]GGGGACTGCTTCTGA	10482
rs749522721	snp	A/G	1.68077e-05	0.00289889	splice-donor-variant	NXF1	GRCh38.p7	11:62805327	CGAAGACCAGCACTT[A/G]CCGCTGTACGACTTC	10482
rs749562717	snp	C/T	1.64757e-05	0.00287012	intron-variant	NXF1	GRCh38.p7	11:62801851	GAGGGCACAGAAAAC[C/T]CTAGGGAAGCCTAAG	10482
rs749588785	snp	G/T	1.64727e-05	0.00286986	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792518	CTCGCCCTTGGCCTG[G/T]AGAAAAATGAAGGTC	10482
rs749694288	snp	A/G	0.000131809	0.00811708	intron-variant	NXF1	GRCh38.p7	11:62796272	TCCCATATTTTGTTC[A/G]TATCACACACTTACT	10482
rs749717363	snp	C/T	1.72955e-05	0.00294065	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794492	ATAACATCATCCTCC[C/T]AACATCATTCCTATT	10482
rs749725935	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62794831	TTTCTCTGATTTCCT[A/G]TTGCCTTTCTGAAAT	10482
rs749749809	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803541	CATGCCAAGTATCAC[C/T]CCGACGGTTAGGTCG	10482
rs749800893	snp	C/T	1.6486e-05	0.00287102	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801169	GTCATCCAGCCTGTA[C/T]AGCCTGTTGTTGCTC	10482
rs749871563	snp	C/T	1.64781e-05	0.00287033	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796089	CGCTTATGTCTACCA[C/T]GAAGGAATTGACGTC	10482
rs749977907	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807190	AGTGGAAACAACCTC[C/T]CCCACTGGCCCCCAG	10482
rs750012097	snp	A/C/T	3.30859e-05	0.00406719	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802216	GCACTTGCTCTGAAT[A/C/T]ATGCTCAGGAGCCAT	10482
rs750029862	snp	A/G	1.66059e-05	0.00288144	synonymous-codon, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800355	AAGGTCCCCAGGAGG[A/G]GAGACACAGGCTACA	10482
rs750101908	snp	C/T	1.68397e-05	0.00290165	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800459	GCTTCAGCCCCTTTA[C/T]CTTGTCCAATTCCCG	10482
rs750228447	snp	A/T	1.84449e-05	0.00303679	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792764	GCCAGCTGAAAGTCC[A/T]CTCCATAAAAGCACC	10482
rs750241407	snp	A/G	1.64846e-05	0.0028709	intron-variant	NXF1	GRCh38.p7	11:62802064	ACAAGAGGAAACAGG[A/G]GCATTACACTGGGAG	10482
rs750291736	snp	A/G			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806199	AGCTCACCAGCAGTG[A/G]CAACTTGCTGGAGAT	10482
rs750376069	snp	C/G			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806100	ACGACATCTGTCAGG[C/G]GTTTGGCGAGCATTG	10482
rs750467601	snp	A/C			utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794307	TAGAGAATGCTTGCA[A/C]CATTTCCTGCTGCTC	10482
rs750511885	snp	A/G	1.64732e-05	0.0028699	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796480	AGGGTTCTGAGGAAT[A/G]AAAGGAATGCTCAGG	10482
rs750512101	snp	A/G	1.64942e-05	0.00287173	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801373	GGGTAGCTGCCATAC[A/G]GCTTCTGCGATTCAG	10482
rs750524963	snp	C/T			utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796545	GCCCTTGTCGGTCTC[C/T]AGAGTCGTAAATTGC	10482
rs750604643	snp	A/C/G	0.000316206	0.0125699	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791797	CGGGGGCCGGGACAC[A/C/G]GCTGCCACAGCCATG	10482
rs750615556	in-del	-/CATCCTGGG	1.65345e-05	0.00287524	cds-indel, nc-transcript-variant	NXF1	GRCh38.p7	11:62803808	ATCGTACTCGGGGAC[-/CATCCTGGG]CATCACTCATTGCCA	10482
rs750724060	snp	A/G	1.64741e-05	0.00286998	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798592	TGTCAAGAACGGGAC[A/G]GAAGTGAGTGATGCT	10482
rs750727442	snp	C/G	1.64912e-05	0.00287147	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803848	ATCTCCATCATCTTC[C/G]TCAAGGCGGGAAGAC	10482
rs750745100	snp	A/G	6.5987e-05	0.00574362	intron-variant	NXF1	GRCh38.p7	11:62801279	CTCCAGCCACTTCCT[A/G]TCTAACACACCCTGC	10482
rs750830166	snp	C/T	6.58892e-05	0.00573936	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797336	GCAGGGCGGTAACGT[C/T]GTGGGGGCTTCAACA	10482
rs750837220	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62803295	TACTCCAGCCTGGGT[A/G]ACAGAGCAAGACTCC	10482
rs750878942	snp	C/G	1.64743e-05	0.00287	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801768	CTTGTTCTGGCTTCA[C/G]TTCATTCAGTATAGT	10482
rs750926382	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802438	TTCTGTCTACTTACA[C/T]TTACTATTTTTTCTT	10482
rs750998818	snp	A/G	6.59402e-05	0.00574158	intron-variant	NXF1	GRCh38.p7	11:62798494	CAGGAATCCTTGTGA[A/G]TGAGAGATGCTGTGC	10482
rs751078673	snp	G/T	3.31664e-05	0.00407211	intron-variant	NXF1	GRCh38.p7	11:62795039	AACAACACCTTAGGG[G/T]CACTAGTGCTTTATG	10482
rs751126844	snp	A/C			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792237	ACAAAGCACCTAAGT[A/C]CTTCGGGTAGTTTAG	10482
rs751177856	snp	A/G	1.64746e-05	0.00287002	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792595	ACCTGACCTCCTGGA[A/G]GCCCAGAGATCCTAG	10482
rs751227205	snp	A/C/T	4.94461e-05	0.00497202	intron-variant	NXF1	GRCh38.p7	11:62802060	AACTACAAGAGGAAA[A/C/T]AGGAGCATTACACTG	10482
rs751291243	snp	C/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806059	TCCCCCACCCCGCCC[C/T]GCCCTGAGTTGCTGA	10482
rs751311479	snp	A/G	1.64776e-05	0.00287028	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798619	TGCTTCAGAGCCACC[A/G]TGCCTCCTGGGCTGC	10482
rs751343079	snp	A/G	5.05881e-05	0.00502906	intron-variant	NXF1	GRCh38.p7	11:62796572	TTGCATAGTACCTAT[A/G]GGAAAAACAAAAAAG	10482
rs751392080	snp	G/T	1.6821e-05	0.00290004	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805368	CCATGCCACAGCGAA[G/T]ATCAAGGGCGGGCTC	10482
rs751428833	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797265	CAGGTATTAGGAACA[C/T]GGAAGCAGTATTCTC	10482
rs751488918	snp	A/C/G	3.36775e-05	0.0041034	intron-variant	NXF1	GRCh38.p7	11:62805317	GTTCCCGACCCGAAG[A/C/G]CCAGCACTTACCGCT	10482
rs751518547	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798723	GTGCTCAGGGAAAAA[G/T]GGCCCCCACTCCCCA	10482
rs751642195	snp	A/G	1.71746e-05	0.00293036	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791791	CGGAACCGGGGGCCG[A/G]GACACGGCTGCCACA	10482
rs751734462	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62801704	TGAGAAGTAGTAAGA[A/C]TGGGTTGGAAACATC	10482
rs751743981	snp	C/G/T	4.94713e-05	0.00497329	intron-variant	NXF1	GRCh38.p7	11:62797407	GAAAGGAAGTAAAAG[C/G/T]TGACAGTGTAGACTG	10482
rs751784990	in-del	-/C	1.67874e-05	0.00289714	intron-variant	NXF1	GRCh38.p7	11:62797138	GGTCTGCCCACCATT[-/C]CCCCTCAACCTCGGG	10482
rs751795206	snp	C/G	1.64768e-05	0.00287021	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794396	CTTTGGATCTCTTCA[C/G]AACTGGCATTCCGCA	10482
rs751895944	snp	C/G	3.29457e-05	0.00405854	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803478	CAGCCCCTCCTCTCT[C/G]TGGAGGAGCTCTGTC	10482
rs751901445	snp	A/C/T	0.000148246	0.00860828	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797333	CTTGCAGGGCGGTAA[A/C/T]GTCGTGGGGGCTTCA	10482
rs751907175	in-del	-/A	1.64803e-05	0.00287052	intron-variant	NXF1	GRCh38.p7	11:62802057	TGAAACTACAAGAGG[-/A]AACAGGAGCATTACA	10482
rs752001134	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62795761	GAGGTAGGCCAAGCC[A/C]AGACGGCTTGGGGGC	10482
rs752016448	snp	A/C	1.65932e-05	0.00288034	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794246	CCCATCCTACACATG[A/C]CCCGCACTCACTTCT	10482
rs752046592	snp	A/G	2.75957e-05	0.00371444	intron-variant	NXF1	GRCh38.p7	11:62804083	GAAGAGATACATACT[A/G]ACGACAGAGGCCATC	10482
rs752115208	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62803578	ATAGGGGTTGCTGTG[A/G]GTAAGCAGAGAATAA	10482
rs752154593	snp	A/G	1.64727e-05	0.00286986	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792523	CCTTGGCCTGGAGAA[A/G]AATGAAGGTCAGTAG	10482
rs752177183	snp	A/G	1.64743e-05	0.00287	intron-variant	NXF1	GRCh38.p7	11:62801657	AAGAAGGGTTTAGTG[A/G]TCACTGGGTTTGTGT	10482
rs752229175	snp	A/G	1.64743e-05	0.00287	intron-variant	NXF1	GRCh38.p7	11:62801927	CTCCAGCCAAGCCAG[A/G]CCCTTTAAACACACC	10482
rs752231209	snp	A/T	1.64779e-05	0.00287031	intron-variant	NXF1	GRCh38.p7	11:62798526	TGTTAGAATGAAAAA[A/T]TTATGGACTTACCAG	10482
rs752294481	snp	A/G	1.64743e-05	0.00287	intron-variant	NXF1	GRCh38.p7	11:62796378	ATGGACGTGGTGTTC[A/G]GAGCAGTGCTGCCAG	10482
rs752306157	snp	G/T			intron-variant	NXF1	GRCh38.p7	11:62804729	CTATGCTTCAGGCAC[G/T]TGATAGGAATGATCT	10482
rs752332719	snp	A/G	1.69893e-05	0.00291451	intron-variant	NXF1	GRCh38.p7	11:62805297	ACCCGCGCCCCAGAT[A/G]GCCAGTTCCCGACCC	10482
rs752356466	snp	A/G	8.40216e-05	0.00648103	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805360	CTCGTCCGCCATGCC[A/G]CAGCGAAGATCAAGG	10482
rs752363594	snp	A/T	1.64735e-05	0.00286993	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792462	GGGGGACTGCTTCTG[A/T]GGCATGACTACGATC	10482
rs752457574	snp	C/T	3.29554e-05	0.00405914	intron-variant	NXF1	GRCh38.p7	11:62796239	CTGAGTTCTGACTGA[C/T]TCCTTCCCATGCCCT	10482
rs752460540	snp	A/G	1.64743e-05	0.00287	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801782	AGTTCATTCAGTATA[A/G]TGTGGGGTGGAGCAG	10482
rs752506043	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803443	GAACCAGTTCTTTGA[A/G]GTCCCATCCTGGCTG	10482
rs752612567	snp	A/C/T	5.58491e-05	0.00528412	synonymous-codon, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800481	CAATTCCCGCTCAGA[A/C/T]TTCAACTGCAAAGGG	10482
rs752634600	snp	A/G	1.70618e-05	0.00292072	intron-variant	NXF1	GRCh38.p7	11:62801066	CTACCCACCCCTTCA[A/G]AAATATAGCCGAGCT	10482
rs752839684	snp	A/T	1.77751e-05	0.00298115	intron-variant	NXF1	GRCh38.p7	11:62802272	GAATCTAGAAATGAG[A/T]GAAAGAGAAAAGAAG	10482
rs752873579	snp	C/T	2.56941e-05	0.00358418	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792798	GTTTGCCAACAAATA[C/T]GTACATTCTTATACA	10482
rs752874861	snp	A/G	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62801640	TGATCAGCTAGAGGA[A/G]AAAGAAGGGTTTAGT	10482
rs752904621	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802799	AAAAGTTCCAAGATA[C/T]TATTTACACCTTGCC	10482
rs752974435	snp	A/G	9.88338e-05	0.00702902	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797324	GCTTCCTACCTTGCA[A/G]GGCGGTAACGTCGTG	10482
rs752984224	in-del	-/AG	4.9423e-05	0.00497082	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792631	TGCCACTGTATTTCC[-/AG]AGACCTTACCTTGAG	10482
rs752996023	snp	A/C/G	6.60048e-05	0.00574445	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800427	CAGGGAGTTTCCATC[A/C/G]AGCCAGAGCTCTTCT	10482
rs753156226	snp	C/G/T	0.000215246	0.0103723	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800442	GAGCCAGAGCTCTTC[C/G/T]AGCTTCAGCCCCTTT	10482
rs753202459	snp	A/C/G	0.000164894	0.0090787	intron-variant	NXF1	GRCh38.p7	11:62795964	AGAGAAGCAGCATCA[A/C/G]GTACAATGTACACTT	10482
rs753209453	in-del	-/TGGTGTTCAGA	1.64747e-05	0.00287003	intron-variant	NXF1	GRCh38.p7	11:62796370	TAAAAGGAATGGACG[-/TGGTGTTCAGA]GCAGTGCTGCCAGCA	10482
rs753268990	snp	C/T	6.62581e-05	0.0057554	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803963	TGAGGGAAATTAACG[C/T]GTTCATCATCGTGTT	10482
rs753366538	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795582	AGCACCACTATGAGA[C/T]GGCTATTACTAACCC	10482
rs753404547	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802567	TCAGCTTTCTGGAGT[A/G]GCTAGGACTACAGGC	10482
rs753424421	snp	A/G	1.70842e-05	0.00292264	intron-variant	NXF1	GRCh38.p7	11:62805288	GCGCCGCCCACCCGC[A/G]CCCCAGATAGCCAGT	10482
rs753447478	snp	C/T	1.73806e-05	0.00294788	intron-variant	NXF1	GRCh38.p7	11:62801049	CAAACTCTCTACACC[C/T]TCTACCCACCCCTTC	10482
rs753491308	snp	A/G	1.6477e-05	0.00287024	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796095	TGTCTACCACGAAGG[A/G]ATTGACGTCGTGCTG	10482
rs753588112	snp	C/T	5.13149e-05	0.00506506	intron-variant	NXF1	GRCh38.p7	11:62804109	CCATCTCCATGCAAA[C/T]TCCGCTCCCTATCCA	10482
rs753609701	snp	A/G	1.74284e-05	0.00295193	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800468	CCTTTATCTTGTCCA[A/G]TTCCCGCTCAGACTT	10482
rs753635689	snp	C/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807389	CCCAAGTACCCTGCA[C/G]AGGCTCAGTGGCAGC	10482
rs753721182	snp	C/T	1.65021e-05	0.00287241	intron-variant	NXF1	GRCh38.p7	11:62802090	GGGAGTCCAGAGCCC[C/T]TGGGGAGGGGCATTA	10482
rs753787457	snp	G/T	1.68046e-05	0.00289862	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802249	CTTGTCATACTTTCT[G/T]CCATAAGGAATCTAG	10482
rs753828711	in-del	-/TA	0.000188484	0.00970599	intron-variant	NXF1	GRCh38.p7	11:62804235	GAGAGAAGCAGGATG[-/TA]GAAATGTGAGACCCA	10482
rs753828999	snp	A/G	3.31967e-05	0.00407397	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794243	ATCCCCATCCTACAC[A/G]TGCCCCGCACTCACT	10482
rs753921712	snp	C/T	1.65127e-05	0.00287334	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797207	AAGTGCAAGACCAGA[C/T]TCTTCAAGTTTTCTG	10482
rs753924116	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799101	GAGGAAAAAGAGAAA[A/G]AGGCAAGATGGGGCA	10482
rs753985738	snp	A/C	1.7821e-05	0.00298499	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807424	GCCACTTGCCTTCCC[A/C]GGAGGGTCCCAAACC	10482
rs754110182	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62796682	CATGCCTGTAATCCC[A/T]GCACTTTGGGAGGCT	10482
rs754146017	snp	A/G	1.64901e-05	0.00287137	intron-variant	NXF1	GRCh38.p7	11:62795952	ATGTGCTCTGAAAGA[A/G]AAGCAGCATCAGGTA	10482
rs754226925	snp	A/G	6.59533e-05	0.00574215	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803857	ATCTTCCTCAAGGCG[A/G]GAAGACCGAATACCA	10482
rs754378828	in-del	-/A	1.64732e-05	0.0028699	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792445	CCAAGGACTATTTAC[-/A]GGGGGGACTGCTTCT	10482
rs754380651	snp	A/G	1.65548e-05	0.002877	intron-variant	NXF1	GRCh38.p7	11:62795025	GCAATAAGAACAGCA[A/G]CAACACCTTAGGGTC	10482
rs754386535	snp	A/G	1.67863e-05	0.00289704	intron-variant	NXF1	GRCh38.p7	11:62803770	AGCCACTAAATTCAA[A/G]CCAGACCAACTGGTC	10482
rs754417161	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802719	TGGGATTACAGGCAT[A/G]AGCCACTGTACCCAG	10482
rs754483244	in-del	-/G			intron-variant	NXF1	GRCh38.p7	11:62794823	ATGTGAGCTTTCTCT[-/G]ATTTCCTGTTGCCTT	10482
rs754551558	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801772	TTCTGGCTTCAGTTC[A/G]TTCAGTATAGTGTGG	10482
rs754611661	snp	C/T	3.2963e-05	0.00405961	intron-variant	NXF1	GRCh38.p7	11:62796225	GCTGCCACACACTCC[C/T]GAGTTCTGACTGATT	10482
rs754657602	snp	A/T	5.93384e-05	0.00544662	intron-variant	NXF1	GRCh38.p7	11:62804115	CCATGCAAACTCCGC[A/T]CCCTATCCACAGGAA	10482
rs754709445	snp	A/G	0.000335514	0.0129478	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792017	CGACTTCCGGGGTGG[A/G]GCTTCCTGCCGCAGA	10482
rs754717700	snp	C/T	3.55082e-05	0.00421341	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800473	ATCTTGTCCAATTCC[C/T]GCTCAGACTTCAACT	10482
rs754726781	snp	A/G			utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794372	GTGGGTGCAGGCATA[A/G]CGAAGGCTCTTTGGA	10482
rs754756653	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62796710	GCTGAGATGGGTGAA[C/T]AGCTTGAGCCCAGGA	10482
rs754771239	snp	C/T	0.000230654	0.0107366	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796097	TCTACCACGAAGGAA[C/T]TGACGTCGTGCTGGG	10482
rs754817717	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62795648	GTTACTTGTCCACAG[A/C]CCCGCACAACCAAAA	10482
rs754879558	snp	A/G	1.64912e-05	0.00287147	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800388	TGACCTGATGTAGGT[A/G]GACTGGTCTCGGAAG	10482
rs754888671	snp	A/C	1.66916e-05	0.00288886	intron-variant	NXF1	GRCh38.p7	11:62804012	ACACAAATTAGAAGT[A/C]AGTAACTGGTCCGGT	10482
rs754950346	snp	C/T	1.75869e-05	0.00296532	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807439	AGGAGGGTCCCAAAC[C/T]CCAACAGAGTGCCTC	10482
rs754956162	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807410	CAGTGGCAGCACTGG[C/T]CACTTGCCTTCCCAG	10482
rs754956879	in-del	-/GTGGCAATGA	0.000193892	0.00984422	intron-variant	NXF1	GRCh38.p7	11:62804241	GCAGGATGTAGAAAT[-/GTGGCAATGA]GTGAGACCCAAAAGT	10482
rs755073225	snp	C/T	1.65858e-05	0.00287969	intron-variant	NXF1	GRCh38.p7	11:62802127	GAGTCCAGCTTGCCC[C/T]TTCACCATCCCTGGT	10482
rs755082194	snp	A/C			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799154	GTATAGGAGACAGAC[A/C]GAAAAAGGAAAGAGA	10482
rs755138772	snp	A/T	4.31965e-05	0.00464719	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792782	CCATAAAAGCACCCA[A/T]GTTTGCCAACAAATA	10482
rs755203879	snp	C/T	3.29766e-05	0.00406045	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797231	TTTTCTGTTCCAAAA[C/T]AGCTTCCCTGAAATC	10482
rs755221416	snp	C/T	2.02227e-05	0.00317977	intron-variant	NXF1	GRCh38.p7	11:62796618	TGGTCTACAGCCATA[C/T]AAGGACCCAGTAGCT	10482
rs755233592	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799820	GGCAAGAGAGACAGA[C/T]TGCATGCCACCAGCC	10482
rs755261012	snp	G/T	1.64912e-05	0.00287147	intron-variant	NXF1	GRCh38.p7	11:62801303	ACCCTGCTTCCTCAT[G/T]CCTAATACTGGGCCA	10482
rs755291439	snp	A/G	1.64882e-05	0.00287121	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803858	TCTTCCTCAAGGCGG[A/G]AAGACCGAATACCAG	10482
rs755300276	snp	C/T	1.64768e-05	0.00287021	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792687	GTGTAGTCCCAGTTG[C/T]TGTCCTGAAGGCACC	10482
rs755380710	snp	A/G	1.65203e-05	0.002874	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801398	ATTCAGGACAACGTC[A/G]ATGTTCTGGGCCACC	10482
rs755424849	snp	A/C	6.62306e-05	0.00575421	intron-variant	NXF1	GRCh38.p7	11:62795028	ATAAGAACAGCAACA[A/C]CACCTTAGGGTCACT	10482
rs755458988	snp	A/C	1.67806e-05	0.00289656	intron-variant	NXF1	GRCh38.p7	11:62803772	CCACTAAATTCAAAC[A/C]AGACCAACTGGTCAC	10482
rs755490015	snp	C/T	4.44692e-05	0.00471515	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791881	GCGGCCCCGATCATG[C/T]TCAAAGAGCAGCACA	10482
rs755543078	snp	C/T	0.0001812	0.00951667	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794356	CGGGCTGGAGGAAGG[C/T]GTGGGTGCAGGCATA	10482
rs755585931	snp	A/G	1.66452e-05	0.00288484	intron-variant	NXF1	GRCh38.p7	11:62803993	TCTAGAGTTAGAAAC[A/G]GGAACACAAATTAGA	10482
rs755618994	snp	A/G	5.6002e-05	0.0052913	intron-variant	NXF1	GRCh38.p7	11:62804186	CTGGAAAACTGTGTA[A/G]GGCTTTTGAAAAATG	10482
rs755636563	snp	C/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806131	TCTTCACAGACCTTC[C/T]ATCAATGGCGTCCCC	10482
rs755639372	snp	A/G	0.000117292	0.00765716	intron-variant	NXF1	GRCh38.p7	11:62804086	GAGATACATACTAAC[A/G]ACAGAGGCCATCTCC	10482
rs755710184	snp	C/T	1.64741e-05	0.00286998	intron-variant	NXF1	GRCh38.p7	11:62801546	CCTATCTGAGAACTA[C/T]TGCTGTCAACCATAC	10482
rs755827175	snp	C/G	8.24015e-05	0.00641825	intron-variant	NXF1	GRCh38.p7	11:62796233	ACACTCCTGAGTTCT[C/G]ACTGATTCCTTCCCA	10482
rs755841238	snp	A/G	1.64781e-05	0.00287033	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796092	TTATGTCTACCACGA[A/G]GGAATTGACGTCGTG	10482
rs755857925	snp	A/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806235	GGAGGACATTTTAAA[A/T]TATCAGGGCCTTGGG	10482
rs755863834	snp	C/T	3.29761e-05	0.00406041	intron-variant	NXF1	GRCh38.p7	11:62802069	AGGAAACAGGAGCAT[C/T]ACACTGGGAGTCCAG	10482
rs755869017	snp	A/G	0.00012788	0.00799523	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791941	CCGGCAGGTGAGCAG[A/G]GGCCGCAGCACGGCT	10482
rs755871305	snp	C/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793612	AGCCCTAGCAGTTGA[C/G]GCTGCAGTGAACTGT	10482
rs755878576	snp	A/C	1.65853e-05	0.00287964	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800357	GGTCCCCAGGAGGGG[A/C]GACACAGGCTACAAC	10482
rs755985871	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792555	GGTAGGCCTACCCTC[A/G]CCACTCAGCAACCCC	10482
rs756025099	snp	G/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801973	TCCAAAATCTTATAG[G/T]TGACAGCCTTCAATG	10482
rs756109157	snp	C/T	1.64741e-05	0.00286998	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792636	ACTGTATTTCCAGAC[C/T]TTACCTTGAGATGAG	10482
rs756115961	in-del	-/GT	3.2987e-05	0.00406108	intron-variant	NXF1	GRCh38.p7	11:62797413	AAGTAAAAGTTGACA[-/GT]GTAGACTGGGCCCAG	10482
rs756128048	snp	A/G			utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805441	GCTCAGGACCGAAGT[A/G]TCCCTACGCCGGGCG	10482
rs756141109	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62796050	AGGCTTCTGTCAGGC[A/G]CAAGCAGGAGCTTAC	10482
rs756165820	in-del	-/ACC	1.6486e-05	0.00287102	cds-indel, nc-transcript-variant	NXF1	GRCh38.p7	11:62803869	GCGGGAAGACCGAAT[-/ACC]AGAACCGCCTCTTCC	10482
rs756215627	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796489	AGGAATGAAAGGAAT[A/G]CTCAGGGAACAGCAG	10482
rs756262183	snp	A/G	0.000247653	0.011125	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791868	GGATGGTGAAGAAGC[A/G]GCCCCGATCATGCTC	10482
rs756268968	snp	A/G	1.90257e-05	0.00308423	intron-variant	NXF1	GRCh38.p7	11:62796605	AGTATGGGCTCTGTG[A/G]TCTACAGCCATACAA	10482
rs756341778	snp	G/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793057	AAATTTTTTATAGAC[G/T]ATCAGGTTTGTGTTT	10482
rs756563433	snp	C/G	3.37245e-05	0.00410623	intron-variant	NXF1	GRCh38.p7	11:62803749	AAAGGGCCATATAAT[C/G]TCATGAGCCACTAAA	10482
rs756641801	snp	G/T	1.64768e-05	0.00287021	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794310	AGAATGCTTGCAACA[G/T]TTCCTGCTGCTCTGG	10482
rs756654784	snp	G/T			intron-variant	NXF1	GRCh38.p7	11:62802489	TCACTCAGGCTGGAG[G/T]GCAGTGGTGCGATCA	10482
rs756744706	snp	C/G	3.33678e-05	0.00408446	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800350	GGGTGAAGGTCCCCA[C/G]GAGGGGAGACACAGG	10482
rs756812295	snp	A/C			upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792317	ATCTTCTGAAGTCTT[A/C]CAGAAGGCAGGCGAG	10482
rs756820640	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62800565	ACCCCCAGTCCCTAC[A/G]CTTAGCTCTGAGATC	10482
rs756847975	snp	A/G	0.000132545	0.0081397	intron-variant	NXF1	GRCh38.p7	11:62802151	CCCTGGTGCCTGGCC[A/G]GCCAGCCACTCAGGC	10482
rs756848721	snp	A/C/T	4.9451e-05	0.00497227	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803877	ACCGAATACCAGAAC[A/C/T]GCCTCTTCCAGACCT	10482
rs756853626	snp	C/T	4.22627e-05	0.00459669	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791890	ATCATGCTCAAAGAG[C/T]AGCACATCCCGTTGC	10482
rs757005579	snp	C/T	1.68196e-05	0.00289992	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805370	ATGCCACAGCGAAGA[C/T]CAAGGGCGGGCTCAG	10482
rs757012820	snp	C/G			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806087	TGAGTCAAATGATAC[C/G]ACATCTGTCAGGGGT	10482
rs757016718	snp	C/T	1.65682e-05	0.00287817	intron-variant	NXF1	GRCh38.p7	11:62795854	TGAGGAAAATTCCAG[C/T]TGGGGGTGGGACCAC	10482
rs757035913	snp	A/G	4.9423e-05	0.00497082	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792624	AGTCTTTTTGCCACT[A/G]TATTTCCAGACCTTA	10482
rs757036659	snp	A/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801803	GGTGGAGCAGAAGAG[A/T]TGATGATGATAGATA	10482
rs757123963	snp	C/T	3.29473e-05	0.00405864	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792431	CCAGACGGTAATATC[C/T]AAGGACTATTTACAG	10482
rs757144957	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62805178	GGAGTCAACAACTCG[A/G]GTGTCCACCTCGAGT	10482
rs757342588	in-del	-/A	0.000301134	0.0122669	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794460	GGACAAAGAGCACTT[-/A]AAAAAGCTAGACAGA	10482
rs757354434	snp	A/G			intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794763	AGGATGAAAACCCAG[A/G]CGGTACAATTCCAGA	10482
rs757458994	snp	C/T	1.65419e-05	0.00287588	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, intron-variant	NXF1, MIR6514	GRCh38.p7	11:62794437	ATCATTTACAATACA[C/T]AGCCTTGAGGACAAA	10482
rs757465119	in-del	-/A	1.65795e-05	0.00287914	splice-donor-variant	NXF1	GRCh38.p7	11:62797180	GACCCTGGGATACTT[-/A]ACTGTTGCAGGAAGT	10482
rs757521035	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803496	GAGGAGCTCTGTCTC[C/T]CCGCACAGTAACATG	10482
rs757582944	in-del	-/AAT			intron-variant	NXF1	GRCh38.p7	11:62798269	CCTGTCTCTACTAAA[-/AAT]ACAAAAATTAGCCAG	10482
rs757675002	snp	C/T	1.64746e-05	0.00287002	intron-variant	NXF1	GRCh38.p7	11:62801659	GAAGGGTTTAGTGGT[C/T]ACTGGGTTTGTGTGT	10482
rs757733240	snp	A/C	8.23771e-05	0.0064173	intron-variant	NXF1	GRCh38.p7	11:62797262	AAACAGGTATTAGGA[A/C]CATGGAAGCAGTATT	10482
rs757752255	snp	G/T	5.60837e-05	0.00529516	intron-variant	NXF1	GRCh38.p7	11:62802293	AGAAAAGAAGGGAAT[G/T]ATAAGTAAGGCTGAA	10482
rs757757070	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799437	TCAGAAGGTGTGAGG[A/G]TTCAGGCCCCTGTAG	10482
rs757929024	snp	C/T	9.99367e-05	0.00706812	intron-variant	NXF1	GRCh38.p7	11:62794893	CCACACTGTTGGCCA[C/T]GGATTAGGACTGGTA	10482

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