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
rs757932214	snp	C/T	1.64779e-05	0.00287031	intron-variant	NXF1	GRCh38.p7	11:62798527	GTTAGAATGAAAAAA[C/T]TATGGACTTACCAGG	10482
rs757982746	snp	A/G	1.6473e-05	0.00286988	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792464	GGGACTGCTTCTGAG[A/G]CATGACTACGATCAC	10482
rs757985494	snp	A/G	1.64765e-05	0.00287019	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798616	TGATGCTTCAGAGCC[A/G]CCGTGCCTCCTGGGC	10482
rs758089394	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801797	GTGTGGGGTGGAGCA[A/G]AAGAGTTGATGATGA	10482
rs758181879	snp	A/G	1.69361e-05	0.00290994	intron-variant	NXF1	GRCh38.p7	11:62805302	CGCCCCAGATAGCCA[A/G]TTCCCGACCCGAAGA	10482
rs758192960	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62803058	GGGTGCGGTGGCTCA[C/T]GCCTATAATCCCAGC	10482
rs758215505	snp	A/G			upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792033	GCTTCCTGCCGCAGA[A/G]CCGCCTTCCGCCCTC	10482
rs758347978	snp	C/G/T	5.07759e-05	0.00503843	intron-variant	NXF1	GRCh38.p7	11:62801072	ACCCCTTCAAAAATA[C/G/T]AGCCGAGCTATCAAT	10482
rs758366032	snp	A/G	1.8144e-05	0.00301193	intron-variant	NXF1	GRCh38.p7	11:62802282	ATGAGAGAAAGAGAA[A/G]AGAAGGGAATGATAA	10482
rs758407665	snp	C/T	3.29571e-05	0.00405924	intron-variant	NXF1	GRCh38.p7	11:62796242	AGTTCTGACTGATTC[C/T]TTCCCATGCCCTTTT	10482
rs758564420	snp	C/T	4.94238e-05	0.00497086	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803446	CCAGTTCTTTGAGGT[C/T]CCATCCTGGCTGGTG	10482
rs758584659	snp	G/T	1.65203e-05	0.002874	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794263	CCGCACTCACTTCTG[G/T]GACCACTCGAGGTTC	10482
rs758629298	snp	C/T	3.21166e-05	0.00400716	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792810	ATATGTACATTCTTA[C/T]ACATCCTTGCACTAT	10482
rs758662879	in-del	-/CAGCTCTGTAAGAACTCTGACTCGTAAATGC	3.30202e-05	0.00406313	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792720	GAGTGGAAGAACAGG[lengthTooLong]CAGCTGAAAGTCCAC	10482
rs758684350	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62794832	TTCTCTGATTTCCTG[C/T]TGCCTTTCTGAAATC	10482
rs758709888	snp	C/T	1.67668e-05	0.00289537	intron-variant	NXF1	GRCh38.p7	11:62797148	CCATTCCCCCTCAAC[C/T]TCGGGGTGGGGAGGG	10482
rs758712000	snp	C/T	3.295e-05	0.00405881	intron-variant	NXF1	GRCh38.p7	11:62801526	CAGATCCCACCTTAT[C/T]ACCACCTATCTGAGA	10482
rs758787324	in-del	-/TA	1.64746e-05	0.00287002	intron-variant	NXF1	GRCh38.p7	11:62796382	CGTGGTGTTCAGAGC[-/TA]AGTGCTGCCAGCAGG	10482
rs758797454	snp	C/T	1.65902e-05	0.00288008	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803973	TAACGCGTTCATCAT[C/T]GTGTTCTAGAGTTAG	10482
rs758859415	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799319	ACAAATCCTTGCTGT[A/G]GTGAGTGGGCACTTG	10482
rs758896739	snp	A/G	1.71681e-05	0.00292981	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807457	AACAGAGTGCCTCAG[A/G]GTAGAGAGGGTTCAA	10482
rs758964860	snp	C/T	1.66813e-05	0.00288797	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791934	GCAGGGGCCGGCAGG[C/T]GAGCAGGGGCCGCAG	10482
rs759065523	snp	A/G	1.65165e-05	0.00287367	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796546	CCCTTGTCGGTCTCC[A/G]GAGTCGTAAATTGCA	10482
rs759074577	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62796663	GTGGCCGGGCATGGA[A/C]GCTCATGCCTGTAAT	10482
rs759126471	snp	A/G	1.68052e-05	0.00289867	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805357	CCCCTCGTCCGCCAT[A/G]CCACAGCGAAGATCA	10482
rs759175745	snp	A/G	1.65029e-05	0.00287248	intron-variant	NXF1	GRCh38.p7	11:62801211	CAATAGCTGTGAGGA[A/G]AGAAGAGTTTAGAGG	10482
rs759200025	snp	C/T	1.64852e-05	0.00287094	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803419	TCTCAAAGTACTCAC[C/T]GTAATCTTGAACCAG	10482
rs759327406	in-del	-/C			intron-variant	NXF1	GRCh38.p7	11:62797952	GCCAACAAGATGAAA[-/C]CCCCCATCTCTACTA	10482
rs759329332	snp	C/G	3.43944e-05	0.00414681	intron-variant	NXF1	GRCh38.p7	11:62801060	CACCCTCTACCCACC[C/G]CTTCAAAAATATAGC	10482
rs759378572	snp	C/T	0.000111514	0.00746622	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791732	AGCGCGGAGCGCAGG[C/T]CGAAGGGGCCACGAT	10482
rs759545990	in-del	-/TC			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793074	TCAGGTTTGTGTTTT[-/TC]TGTTTGCTTTTTTTT	10482
rs759609846	snp	G/T	1.64741e-05	0.00286998	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794362	GGAGGAAGGCGTGGG[G/T]GCAGGCATAGCGAAG	10482
rs759623192	snp	C/G	0.00011302	0.00751646	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791958	GCCGCAGCACGGCTA[C/G]CAGCCCCGTGGGCCA	10482
rs759634672	in-del	-/CACT			intron-variant	NXF1	GRCh38.p7	11:62805011	AGCCCACGAGCAGGG[-/CACT]CACTCACATTAAAGG	10482
rs759688161	snp	A/G	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62797307	GTTCTTACTCTGTCC[A/G]TGCTTCCTACCTTGC	10482
rs759744324	in-del	-/G			intron-variant	NXF1	GRCh38.p7	11:62804847	TTCAACCTCCACCAC[-/G]CACTCCTAACTTACT	10482
rs759746384	snp	C/T	2.10289e-05	0.00324253	intron-variant	NXF1	GRCh38.p7	11:62804065	TAGTACTCTGAACTA[C/T]TGGAAGAGATACATA	10482
rs759856894	snp	C/T	1.78207e-05	0.00298497	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791989	TCGCCTCCAAGGCGC[C/T]GCCATGGCCAGCCGA	10482
rs760103010	snp	G/T	1.71059e-05	0.00292449	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800339	AGCCTCCCAGGGGGT[G/T]AAGGTCCCCAGGAGG	10482
rs760134223	snp	A/G	1.64814e-05	0.00287061	intron-variant	NXF1	GRCh38.p7	11:62796200	TGGGTAGAGGAGAAA[A/G]CTCAGTGGTGCTGCC	10482
rs760141073	in-del	-/G	1.64814e-05	0.00287061	intron-variant	NXF1	GRCh38.p7	11:62796196	GCTGTGGGTAGAGGA[-/G]AAAGCTCAGTGGTGC	10482
rs760157898	snp	C/G	1.65108e-05	0.00287317	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800433	GTTTCCATCGAGCCA[C/G]AGCTCTTCTAGCTTC	10482
rs760158056	snp	A/C	1.64909e-05	0.00287144	intron-variant	NXF1	GRCh38.p7	11:62795954	GTGCTCTGAAAGAGA[A/C]GCAGCATCAGGTACA	10482
rs760207921	snp	C/G	4.94719e-05	0.00497328	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801193	GTTGCTCAAGTTCAA[C/G]GACAATAGCTGTGAG	10482
rs760268349	snp	A/G/T	1.78144e-05	0.00298444	intron-variant	NXF1	GRCh38.p7	11:62796588	GGAAAAACAAAAAAG[A/G/T]AAGTATGGGCTCTGT	10482
rs760313681	snp	A/G	1.73712e-05	0.00294708	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791725	GCGCCAGAGCGCGGA[A/G]CGCAGGTCGAAGGGG	10482
rs760318474	snp	C/T	1.65012e-05	0.00287234	intron-variant	NXF1	GRCh38.p7	11:62803395	CTATCTCTACTGTAC[C/T]ATCTACTTTCTCAAA	10482
rs760371430	snp	C/G	2.31763e-05	0.00340406	intron-variant	NXF1	GRCh38.p7	11:62800517	GGAACAAAGGGAGGA[C/G]ACCCTGGTGAAGACA	10482
rs760472591	snp	A/C/T	0.000143627	0.00847305	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791994	TCCAAGGCGCCGCCA[A/C/T]GGCCAGCCGACTTCC	10482
rs760514017	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801595	CTTTGAGGTCAAGGG[C/T]TTGTTGGGAGCCATC	10482
rs760568773	snp	C/T	3.32502e-05	0.00407725	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794238	AGTGCATCCCCATCC[C/T]ACACATGCCCCGCAC	10482
rs760646749	snp	C/T			missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801753	CCTTTAGCTGTTCTA[C/T]TTGTTCTGGCTTCAG	10482
rs760677295	snp	C/T	3.31686e-05	0.00407225	intron-variant	NXF1	GRCh38.p7	11:62797178	GGGGACCCTGGGATA[C/T]TTACTGTTGCAGGAA	10482
rs760723083	snp	A/G	0.000197677	0.0099398	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798612	TGAGTGATGCTTCAG[A/G]GCCACCGTGCCTCCT	10482
rs760732496	snp	A/G	3.29473e-05	0.00405864	intron-variant	NXF1	GRCh38.p7	11:62797298	CACACACAAGTTCTT[A/G]CTCTGTCCATGCTTC	10482
rs760734565	snp	A/G	1.96612e-05	0.00313532	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792775	GTCCACTCCATAAAA[A/G]CACCCAAGTTTGCCA	10482
rs760779034	snp	C/T	1.64906e-05	0.00287142	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803849	TCTCCATCATCTTCC[C/T]CAAGGCGGGAAGACC	10482
rs760816567	snp	A/T	3.32995e-05	0.00408027	intron-variant	NXF1	GRCh38.p7	11:62801451	AAGGAAAGGGAAGAC[A/T]GAGAGGGTTTGCCCA	10482
rs760946196	snp	A/G	7.75555e-05	0.00622669	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791924	GTCGTGCCTTGCAGG[A/G]GCCGGCAGGTGAGCA	10482
rs760981166	in-del	-/A			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806320	TTCAACTTCCTTTGG[-/A]AATGTATGAGACAGG	10482
rs761015334	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62803320	GACTCCATTTAAAAA[A/T]AATAATAATAATAAT	10482
rs761041885	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804531	TGGAATGCTCTCCAG[A/G]AAGATGACCTTCTGA	10482
rs761132527	snp	A/G	1.65192e-05	0.00287391	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62795007	CGGGACTTTCCGTCC[A/G]CTGCAATAAGAACAG	10482
rs761181910	snp	A/G	8.25893e-05	0.00642556	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802186	TCTTACCTCAATAGG[A/G]GTGAAGGGCACACTG	10482
rs761237210	snp	C/T	1.66015e-05	0.00288105	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800445	CCAGAGCTCTTCTAG[C/T]TTCAGCCCCTTTATC	10482
rs761240108	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62802302	GGGAATGATAAGTAA[A/G]GCTGAATAGCAGACC	10482
rs761256260	snp	C/T	1.64762e-05	0.00287016	intron-variant	NXF1	GRCh38.p7	11:62801909	CTGAGCACCAACCTC[C/T]ACCTCCAGCCAAGCC	10482
rs761309362	snp	A/G	3.29462e-05	0.00405857	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802011	AGTACTGGCGTCTTC[A/G]ACGAAGAACTGGGCC	10482
rs761411901	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793468	TATAACCGCAGCACT[C/T]TGGGAGGCCTAGGTG	10482
rs761436780	in-del	-/CCGCCTT			upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792033	CTTCCTGCCGCAGAG[-/CCGCCTT]CCGCCTTCCGCCCTC	10482
rs761439860	snp	G/T	1.66765e-05	0.00288756	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794229	CCCTACTTCAGTGCA[G/T]CCCCATCCTACACAT	10482
rs761473671	snp	A/C	3.45991e-05	0.00415913	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792752	TGACTCGTAAATGCC[A/C]GCTGAAAGTCCACTC	10482
rs761495389	in-del	-/CC	1.65464e-05	0.00287627	intron-variant	NXF1	GRCh38.p7	11:62795995	CTCAGAGCCTGAGTG[-/CC]CCCCCTTGCCTATTA	10482
rs761615212	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798912	AGCCCCGGGAGGAGG[C/G]AATGGGGTGGGAGCC	10482
rs761838693	snp	C/T	4.94597e-05	0.00497266	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801354	TTCTCTTCAATGATC[C/T]TCAGGGTAGCTGCCA	10482
rs761840868	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803908	ACGGTTTCCTTCACC[A/G]TATTTCCACCGGAAG	10482
rs761895791	snp	A/G	1.66396e-05	0.00288436	intron-variant	NXF1	GRCh38.p7	11:62801445	GAAGGGAAGGAAAGG[A/G]AAGACTGAGAGGGTT	10482
rs761928115	snp	C/G	1.64743e-05	0.00287	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798589	CGCTGTCAAGAACGG[C/G]ACAGAAGTGAGTGAT	10482
rs761982656	snp	A/C/G/T	0.00010058	0.00709095	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791867	AGGATGGTGAAGAAG[A/C/G/T]GGCCCCGATCATGCT	10482
rs762064065	snp	A/G	1.64982e-05	0.00287208	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794983	CGGGTGAAGGCTCGC[A/G]AAGAATCCCGGGACT	10482
rs762072016	in-del	-/AA	1.77915e-05	0.00298252	intron-variant	NXF1	GRCh38.p7	11:62802274	ATCTAGAAATGAGAG[-/AA]AGAGAAAAGAAGGGA	10482
rs762101632	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62802398	AGGTTTTCTACTTGA[C/G]ATACACATAGATTCT	10482
rs762210673	in-del	-/AC			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799148	GGGGAGGTATAGGAG[-/AC]AGACAGAAAAAGGAA	10482
rs762222998	snp	A/G	1.67987e-05	0.00289811	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62805333	CCAGCACTTACCGCT[A/G]TACGACTTCCCCTCG	10482
rs762359945	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62795274	CGAGGTCAAGAGATC[A/G]AGACCATCCTGTCCA	10482
rs762373822	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802031	AGAACTGGGCCCGTG[C/T]ATTCTCATAGTGAAA	10482
rs762440318	snp	A/G	6.58913e-05	0.00573945	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792451	ACTATTTACAGGGGG[A/G]ACTGCTTCTGAGGCA	10482
rs762632441	snp	A/G	1.68131e-05	0.00289935	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805363	GTCCGCCATGCCACA[A/G]CGAAGATCAAGGGCG	10482
rs762656902	snp	C/G	1.67497e-05	0.00289389	splice-acceptor-variant	NXF1	GRCh38.p7	11:62796568	TAAATTGCATAGTAC[C/G]TATGGGAAAAACAAA	10482
rs762683834	snp	C/G	8.23676e-05	0.00641693	intron-variant	NXF1	GRCh38.p7	11:62796384	GTGGTGTTCAGAGCA[C/G]TGCTGCCAGCAGGTG	10482
rs762695933	in-del	-/CGC	0.000672947	0.0183309	cds-indel, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791986	CCATCGCCTCCAAGG[-/CGC]CGCCATGGCCAGCCG	10482
rs762722317	in-del	-/GCAGGGGCCGGCAGGTGA	0.000419175	0.0144711	cds-indel, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791918	GCAGCGTCGTGCCTT[-/GCAGGGGCCGGCAGGTGA]GCAGGGGCCGGCAGG	10482
rs762843964	snp	A/C/T	3.30421e-05	0.0040645	intron-variant	NXF1	GRCh38.p7	11:62801227	AGAAGAGTTTAGAGG[A/C/T]GGCACCACCAGCAAG	10482
rs762854073	snp	C/G	5.26912e-05	0.00513253	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791850	CCGCGCAGAACAGCC[C/G]GAGGATGGTGAAGAA	10482
rs762877900	snp	A/G	1.70991e-05	0.00292391	stop-gained, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791772	CCGCATCCAGAGGCT[A/G]CACCGGAACCGGGGG	10482
rs762976877	snp	C/T	1.64901e-05	0.00287137	intron-variant	NXF1	GRCh38.p7	11:62803596	AAGCAGAGAATAAAA[C/T]GACCACAAATGCTAG	10482
rs763032090	snp	C/T	1.65247e-05	0.00287438	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803812	TACTCGGGGACCATC[C/T]TGGGCATCACTCATT	10482
rs763055591	snp	A/G	4.94205e-05	0.0049707	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798581	GCGAATGGCGCTGTC[A/G]AGAACGGGACAGAAG	10482
rs763128808	snp	C/T	1.64738e-05	0.00286995	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794373	TGGGTGCAGGCATAG[C/T]GAAGGCTCTTTGGAT	10482
rs763160052	snp	C/T	3.29478e-05	0.00405867	intron-variant	NXF1	GRCh38.p7	11:62801729	AACATCTAATTTGAG[C/T]CTGCCTCACCTTTAG	10482
rs763213550	snp	A/G	1.64871e-05	0.00287111	intron-variant	NXF1	GRCh38.p7	11:62797400	TCCTGTGGAAAGGAA[A/G]TAAAAGTTGACAGTG	10482
rs763242188	snp	A/G	0.000198079	0.00994988	intron-variant	NXF1	GRCh38.p7	11:62804239	GAAGCAGGATGTAGA[A/G]ATGTGAGACCCAAAA	10482
rs763309893	snp	A/G	1.64727e-05	0.00286986	intron-variant	NXF1	GRCh38.p7	11:62801646	GCTAGAGGAAAAAGA[A/G]GGGTTTAGTGGTCAC	10482
rs763326880	snp	A/C	7.49223e-05	0.00612009	intron-variant	NXF1	GRCh38.p7	11:62804077	CTATTGGAAGAGATA[A/C]ATACTAACGACAGAG	10482
rs763384939	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62795462	GCCTGGTGATAGAGT[A/G]TGACTCCATCTCAAA	10482
rs763385260	in-del	-/GAGGGAAGACACA	3.29489e-05	0.00405874	intron-variant	NXF1	GRCh38.p7	11:62801823	GATGATAGATATCTG[-/GAGGGAAGACACA]GAGGGCACAGAAAAC	10482
rs763506805	snp	A/G	2.23556e-05	0.00334325	intron-variant	NXF1	GRCh38.p7	11:62800512	TGGAAGGAACAAAGG[A/G]AGGAGACCCTGGTGA	10482
rs763597745	snp	C/T	1.64803e-05	0.00287052	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796175	TTCAGCAGCCGGAAC[C/T]GCAAGGCTGTGGGTA	10482
rs763600489	snp	C/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802035	CTGGGCCCGTGTATT[C/G]TCATAGTGAAACTAC	10482
rs763652657	snp	A/C			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806022	ATATATTTGTGAAAT[A/C]AATGAATTTGTGTTA	10482
rs763684051	snp	G/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801948	TAAACACACCCTTCG[G/T]TTCTCCCGATCCAAA	10482
rs763717765	snp	C/G	1.64789e-05	0.0028704	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792564	ACCCTCGCCACTCAG[C/G]AACCCCACTCAGCTA	10482
rs763741054	snp	C/G	1.64857e-05	0.00287099	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801334	AAGGCCTTACCTCAG[C/G]GATGTTCTCTTCAAT	10482
rs763814790	in-del	-/GCAGGGGCCGGCAGGTGA	0.000419175	0.0144711	cds-indel, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791919	GCAGCGTCGTGCCTT[-/GCAGGGGCCGGCAGGTGA]GCAGGGGCCGCAGCA	10482
rs763836933	snp	A/C/G	0.000169043	0.00919211	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805402	CGCTGGCCGCTACGC[A/C/G]GGCAAACAACCTAAC	10482
rs763839214	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62804936	CTCGAATATTAAGCC[A/C]AAGCCCAGGCCCGAG	10482
rs763841957	snp	A/C	1.68128e-05	0.00289933	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805364	TCCGCCATGCCACAG[A/C]GAAGATCAAGGGCGG	10482
rs763848255	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62801559	TACTGCTGTCAACCA[C/T]ACCTGGGTCTGAACG	10482
rs763864427	snp	A/G	3.35892e-05	0.00409798	intron-variant	NXF1	GRCh38.p7	11:62796570	AATTGCATAGTACCT[A/G]TGGGAAAAACAAAAA	10482
rs763879522	snp	A/G	1.64738e-05	0.00286995	intron-variant	NXF1	GRCh38.p7	11:62796428	CTGGGAAACCCAGTG[A/G]TCCCGGGCAGATTCT	10482
rs764043914	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62803176	ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGGGT	10482
rs764067665	snp	A/G	5.12492e-05	0.00506182	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791857	GAACAGCCCGAGGAT[A/G]GTGAAGAAGCGGCCC	10482
rs764144716	snp	A/G	0.000255656	0.0113032	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791787	GCACCGGAACCGGGG[A/G]CCGGGACACGGCTGC	10482
rs764256179	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803459	GTCCCATCCTGGCTG[A/G]TGCCAGCCCCTCCTC	10482
rs764307538	snp	G/T	4.94719e-05	0.00497328	intron-variant	NXF1	GRCh38.p7	11:62803597	AGCAGAGAATAAAAT[G/T]ACCACAAATGCTAGG	10482
rs764384592	in-del	-/TG	1.64738e-05	0.00286995	intron-variant	NXF1	GRCh38.p7	11:62796448	GGGCAGATTCTGGGA[-/TG]TGATACTAACCGGGC	10482
rs764488171	snp	A/G	9.88728e-05	0.00703041	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796180	CAGCCGGAACCGCAA[A/G]GCTGTGGGTAGAGGA	10482
rs764511048	in-del	-/AC	1.64751e-05	0.00287007	intron-variant	NXF1	GRCh38.p7	11:62801831	ATATCTGGAGGGAAG[-/AC]ACAGAGGGCACAGAA	10482
rs764514672	snp	G/T	2.71249e-05	0.00368262	intron-variant	NXF1	GRCh38.p7	11:62804082	GGAAGAGATACATAC[G/T]AACGACAGAGGCCAT	10482
rs764551667	in-del	-/A	4.96471e-05	0.00498208	intron-variant	NXF1	GRCh38.p7	11:62795023	TGCAATAAGAACAGC[-/A]AACAACACCTTAGGG	10482
rs764575573	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62795474	AGTGTGACTCCATCT[A/C]AAAAAAAAGTAATAA	10482
rs764612194	in-del	-/T			intron-variant	NXF1	GRCh38.p7	11:62800606	TTTTAAAATTTTTTC[-/T]TTTTTTTTTTTTTTT	10482
rs764680480	snp	G/T	1.64732e-05	0.0028699	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792458	ACAGGGGGGACTGCT[G/T]CTGAGGCATGACTAC	10482
rs764786815	snp	C/G	1.68071e-05	0.00289884	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805358	CCCTCGTCCGCCATG[C/G]CACAGCGAAGATCAA	10482
rs764844417	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62796369	ATAAAAGGAATGGAC[C/G]TGGTGTTCAGAGCAG	10482
rs764886389	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799904	CTGAGAAAAGGGTCC[C/T]TCTTGGCGCAAGGGC	10482
rs764894636	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795709	CAAAGTCCTCCTAAT[C/T]CCCAGGCTTTTCCCA	10482
rs764915618	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62796884	CCAGCCTGGCCAACA[C/T]AGTGAAATCCCATCT	10482
rs765003549	snp	C/G	1.6507e-05	0.00287284	intron-variant	NXF1	GRCh38.p7	11:62801216	GCTGTGAGGAGAGAA[C/G]AGTTTAGAGGAGGCA	10482
rs765024234	snp	C/G	1.71781e-05	0.00293066	intron-variant	NXF1	GRCh38.p7	11:62801061	ACCCTCTACCCACCC[C/G]TTCAAAAATATAGCC	10482
rs765088112	snp	C/T	9.82946e-05	0.00700982	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791755	GCCACGATTTGGGAC[C/T]TCCGCATCCAGAGGC	10482
rs765158791	snp	C/T	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62797311	TTACTCTGTCCATGC[C/T]TCCTACCTTGCAGGG	10482
rs765185841	snp	A/C/T	3.29474e-05	0.00405867	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794368	AGGCGTGGGTGCAGG[A/C/T]ATAGCGAAGGCTCTT	10482
rs765247146	snp	A/G	8.23744e-05	0.0064172	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803441	TTGAACCAGTTCTTT[A/G]AGGTCCCATCCTGGC	10482
rs765279210	snp	A/C	1.74583e-05	0.00295446	intron-variant	NXF1	GRCh38.p7	11:62802266	CATAAGGAATCTAGA[A/C]ATGAGAGAAAGAGAA	10482
rs765289275	snp	C/T	4.97302e-05	0.00498624	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794249	ATCCTACACATGCCC[C/T]GCACTCACTTCTGGG	10482
rs765473082	snp	A/C			intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794175	GTCTCCAAAAAAAAA[A/C]CAAAAAAACTGTCAG	10482
rs765474231	snp	C/G	4.02018e-05	0.00448322	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791932	TTGCAGGGGCCGGCA[C/G]GTGAGCAGGGGCCGC	10482
rs765517125	snp	G/T	8.24002e-05	0.0064182	intron-variant	NXF1	GRCh38.p7	11:62797245	ATAGCTTCCCTGAAA[G/T]CAAACAGGTATTAGG	10482
rs765531315	in-del	-/TTA			intron-variant	NXF1	GRCh38.p7	11:62802773	AAAAAAAAATCAATT[-/TTA]TTTATTCTAAAAGTT	10482
rs765532603	snp	A/C/G	5.05165e-05	0.00502551	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791953	CAGGGGCCGCAGCAC[A/C/G]GCTAGCAGCCCCGTG	10482
rs765562764	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799207	CTACAAGGCAAAAAA[A/G]CATCTAGAAAAATGA	10482
rs765569650	snp	A/G	6.62186e-05	0.00575369	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803962	TTGAGGGAAATTAAC[A/G]CGTTCATCATCGTGT	10482
rs765626592	snp	A/G/T	3.29501e-05	0.00405884	intron-variant	NXF1	GRCh38.p7	11:62801525	ACAGATCCCACCTTA[A/G/T]CACCACCTATCTGAG	10482
rs765628110	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62801260	GATCAGAGACGAATC[A/T]GCCCTCCAGCCACTT	10482
rs765628690	snp	A/G	2.15729e-05	0.0032842	intron-variant	NXF1	GRCh38.p7	11:62804068	TACTCTGAACTATTG[A/G]AAGAGATACATACTA	10482
rs765634318	in-del	-/GGGAATAAAAGGAATGGA	1.64735e-05	0.00286993	intron-variant	NXF1	GRCh38.p7	11:62796350	CTAAGCTGCTTCTGG[-/GGGAATAAAAGGAATGGA]CGTGGTGTTCAGAGC	10482
rs765635190	snp	C/G/T	1.80935e-05	0.00300773	utr-variant-5-prime, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791995	CCAAGGCGCCGCCAT[C/G/T]GCCAGCCGACTTCCG	10482
rs765635210	snp	C/T	1.64991e-05	0.00287215	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796066	CAAGCAGGAGCTTAC[C/T]GTCTGGGCGCTTATG	10482
rs765695282	in-del	-/TG	0.000115313	0.0075923	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792623	TAGTCTTTTTGCCAC[-/TG]TATTTCCAGACCTTA	10482
rs765695453	snp	A/C	6.09069e-05	0.00551813	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791962	CAGCACGGCTAGCAG[A/C]CCCGTGGGCCATCGC	10482
rs765813168	snp	C/G	1.64912e-05	0.00287147	intron-variant	NXF1	GRCh38.p7	11:62795956	GCTCTGAAAGAGAAG[C/G]AGCATCAGGTACAAT	10482
rs765848690	snp	C/T	1.64827e-05	0.00287073	intron-variant	NXF1	GRCh38.p7	11:62796219	AGTGGTGCTGCCACA[C/T]ACTCCTGAGTTCTGA	10482
rs765926298	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793662	AGCCTGGGCATCAGA[A/G]TGAGACCCTGTCTCA	10482
rs765970936	snp	A/G	1.64773e-05	0.00287026	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796093	TATGTCTACCACGAA[A/G]GAATTGACGTCGTGC	10482
rs765980043	snp	C/T	1.88485e-05	0.00306984	utr-variant-5-prime, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792007	CATGGCCAGCCGACT[C/T]CCGGGGTGGGGCTTC	10482
rs765984423	snp	A/G	3.22087e-05	0.00401289	intron-variant	NXF1	GRCh38.p7	11:62804092	CATACTAACGACAGA[A/G]GCCATCTCCATGCAA	10482
rs766038689	snp	C/T	1.71021e-05	0.00292416	intron-variant	NXF1	GRCh38.p7	11:62805283	GGCCGGCGCCGCCCA[C/T]CCGCGCCCCAGATAG	10482
rs766044262	snp	C/T	6.96731e-05	0.00590184	intron-variant	NXF1	GRCh38.p7	11:62801048	ACAAACTCTCTACAC[C/T]CTCTACCCACCCCTT	10482
rs766049113	snp	C/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807291	TGAGGGTGGTGGGGG[C/G]AGGACAGGGTGGCCA	10482
rs766123553	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62795482	TCCATCTCAAAAAAA[A/T]GTAATAACTACTAAT	10482
rs766152776	snp	C/T	0.000198715	0.00996584	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802222	GCTCTGAATCATGCT[C/T]AGGAGCCATGCCTTG	10482
rs766180329	snp	A/G	1.68926e-05	0.0029062	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805408	CCGCTACGCCGGCAA[A/G]CAACCTAACTCCCAA	10482
rs766204023	snp	C/T	1.71965e-05	0.00293222	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800466	CCCCTTTATCTTGTC[C/T]AATTCCCGCTCAGAC	10482
rs766204396	snp	C/T	3.29935e-05	0.00406149	intron-variant	NXF1	GRCh38.p7	11:62803397	ATCTCTACTGTACCA[C/T]CTACTTTCTCAAAGT	10482
rs766235809	snp	C/T	9.96628e-05	0.00705843	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794242	CATCCCCATCCTACA[C/T]ATGCCCCGCACTCAC	10482
rs766308975	snp	A/C	1.64727e-05	0.00286986	intron-variant	NXF1	GRCh38.p7	11:62801466	TGAGAGGGTTTGCCC[A/C]TGCCAGCATTAGCAG	10482
rs766379940	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802499	TGGAGTGCAGTGGTG[C/T]GATCATAGCTCACTG	10482
rs766397123	snp	C/T	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62797299	ACACACAAGTTCTTA[C/T]TCTGTCCATGCTTCC	10482
rs766538202	snp	C/T	4.95062e-05	0.004975	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803938	GGGACCCCGGCCTTT[C/T]TTCTTTCTTTGAGGG	10482
rs766585369	snp	A/G	3.30972e-05	0.00406786	intron-variant	NXF1	GRCh38.p7	11:62795022	ACTGCAATAAGAACA[A/G]CAACAACACCTTAGG	10482
rs766604114	snp	C/T	0.00011692	0.00764503	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791926	CGTGCCTTGCAGGGG[C/T]CGGCAGGTGAGCAGG	10482
rs766631420	snp	G/T	1.65149e-05	0.00287353	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797205	GGAAGTGCAAGACCA[G/T]ACTCTTCAAGTTTTC	10482
rs766680799	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804536	TGCTCTCCAGGAAGA[C/T]GACCTTCTGATTCAT	10482
rs766815532	snp	C/T	1.64749e-05	0.00287005	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798604	GACAGAAGTGAGTGA[C/T]GCTTCAGAGCCACCG	10482
rs766820705	snp	A/C	1.64893e-05	0.0028713	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803855	TCATCTTCCTCAAGG[A/C]GGGAAGACCGAATAC	10482
rs766823161	snp	C/G	1.64906e-05	0.00287142	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62795939	GAAAAACACAGCAAT[C/G]TGCTCTGAAAGAGAA	10482
rs766998737	snp	C/T	1.66117e-05	0.00288194	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800448	GAGCTCTTCTAGCTT[C/T]AGCCCCTTTATCTTG	10482
rs767077918	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793540	AAATTAGCCAGGTGC[C/T]GTGGCCTATGCCTGT	10482
rs767082319	in-del	-/AC	1.64732e-05	0.0028699	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792436	CGGTAATATCCAAGG[-/AC]TATTTACAGGGGGGA	10482
rs767103079	snp	A/G	1.65946e-05	0.00288046	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803974	AACGCGTTCATCATC[A/G]TGTTCTAGAGTTAGA	10482
rs767105224	snp	A/G/T	4.05737e-05	0.00450391	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791935	CAGGGGCCGGCAGGT[A/G/T]AGCAGGGGCCGCAGC	10482
rs767109813	snp	C/G	1.66228e-05	0.0028829	missense, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800353	TGAAGGTCCCCAGGA[C/G]GGGAGACACAGGCTA	10482
rs767125400	snp	C/T	1.64798e-05	0.00287047	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796084	CTGGGCGCTTATGTC[C/T]ACCACGAAGGAATTG	10482
rs767188021	snp	A/G	8.25893e-05	0.00642556	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62802192	CTCAATAGGGGTGAA[A/G]GGCACACTGCACTTG	10482
rs767206819	in-del	-/C	1.64798e-05	0.00287047	splice-acceptor-variant	NXF1	GRCh38.p7	11:62796182	GCCGGAACCGCAAGG[-/C]TGTGGGTAGAGGAGA	10482
rs767258004	snp	A/G			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806138	AGACCTTCCATCAAT[A/G]GCGTCCCCTACTAGA	10482
rs767275181	snp	A/G	8.95921e-05	0.00669238	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792760	AAATGCCAGCTGAAA[A/G]TCCACTCCATAAAAG	10482
rs767278618	snp	C/T	1.64743e-05	0.00287	upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792627	CTTTTTGCCACTGTA[C/T]TTCCAGACCTTACCT	10482
rs767345792	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807149	TTCCTTTGGGAGAGG[C/T]TGGAGAGGGTTTATA	10482
rs767588645	snp	C/T			missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791918	TGCAGCGTCGTGCCT[C/T]GCAGGGGCCGGCAGG	10482
rs767602450	in-del	-/AAG	3.62812e-05	0.00425902	intron-variant	NXF1	GRCh38.p7	11:62802282	ATGAGAGAAAGAGAA[-/AAG]AAGGGAATGATAAGT	10482
rs767695353	snp	C/G	1.65386e-05	0.00287559	intron-variant	NXF1	GRCh38.p7	11:62801250	CCAGCAAGTGGATCA[C/G]AGACGAATCTGCCCT	10482
rs767716720	snp	A/G	1.64879e-05	0.00287118	intron-variant	NXF1	GRCh38.p7	11:62798490	TATCCAGGAATCCTT[A/G]TGAGTGAGAGATGCT	10482
rs767746214	snp	C/T	1.6489e-05	0.00287128	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801361	CAATGATCCTCAGGG[C/T]AGCTGCCATACAGCT	10482
rs767785508	snp	A/C/G	4.9513e-05	0.00497538	intron-variant	NXF1	GRCh38.p7	11:62803616	ACAAATGCTAGGAAA[A/C/G]TCTTCTCAAAGGCCT	10482
rs767889099	snp	A/C	1.64735e-05	0.00286993	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792452	CTATTTACAGGGGGG[A/C]CTGCTTCTGAGGCAT	10482
rs767938333	snp	C/G	3.32149e-05	0.00407509	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794444	ACAATACATAGCCTT[C/G]AGGACAAAGAGCACT	10482
rs767944388	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801761	TGTTCTACTTGTTCT[A/G]GCTTCAGTTCATTCA	10482
rs767994563	snp	A/C	1.64741e-05	0.00286998	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798591	CTGTCAAGAACGGGA[A/C]AGAAGTGAGTGATGC	10482
rs768011819	snp	A/G	1.64751e-05	0.00287007	intron-variant	NXF1	GRCh38.p7	11:62797269	TATTAGGAACATGGA[A/G]GCAGTATTCTCTCCA	10482
rs768066926	snp	G/T	0.000116941	0.00764569	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794220	TACTACTAGCCCTAC[G/T]TCAGTGCATCCCCAT	10482
rs768118174	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792744	AAGAACTCTGACTCG[C/T]AAATGCCAGCTGAAA	10482
rs768293846	snp	C/G	1.66128e-05	0.00288204	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791909	ACATCCCGTTGCAGC[C/G]TCGTGCCTTGCAGGG	10482
rs768336189	snp	C/G/T	3.33401e-05	0.00408279	intron-variant	NXF1	GRCh38.p7	11:62797162	CCTCGGGGTGGGGAG[C/G/T]GGGGACCCTGGGATA	10482
rs768469920	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800083	TAGAAAGGGGAGATG[C/G]CTTTCCTGGAACAAC	10482
rs768509567	snp	C/T	0.000147351	0.00858219	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791950	GAGCAGGGGCCGCAG[C/T]ACGGCTAGCAGCCCC	10482
rs768529161	in-del	-/C	0.104938	0.20361	intron-variant	NXF1	GRCh38.p7	11:62795994	CTCAGAGCCTGAGTG[-/C]CCCCCCCTTGCCTAT	10482
rs768552145	snp	A/G	1.65026e-05	0.00287246	intron-variant	NXF1	GRCh38.p7	11:62795891	AACTCGGGACTCTAA[A/G]GATTCTTACCTTCCT	10482
rs768563196	snp	A/G	1.6628e-05	0.00288335	intron-variant	NXF1	GRCh38.p7	11:62801435	TCAGGAAGCAGAAGG[A/G]AAGGAAAGGGAAGAC	10482
rs768580550	in-del	-/GCCCCTTT	1.66252e-05	0.00288311	frameshift-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800449	GCTCTTCTAGCTTCA[-/GCCCCTTT]GCCCCTTTATCTTGT	10482
rs768601243	in-del	-/GAA			cds-indel, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791860	CAGCCCGAGGATGGT[-/GAA]GAAGCGGCCCCGATC	10482
rs768660323	snp	C/G	1.64741e-05	0.00286998	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798586	TGGCGCTGTCAAGAA[C/G]GGGACAGAAGTGAGT	10482
rs768718317	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801987	GTTGACAGCCTTCAA[C/T]GCAGAGGCAGTACTG	10482
rs768745939	snp	C/T	4.94972e-05	0.00497455	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803834	TCACTCATTGCCACA[C/T]CTCCATCATCTTCCT	10482
rs768783153	snp	A/G	4.81371e-05	0.00490573	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800298	CACATCTCCGCAGAC[A/G]GGCCCTGGTCAGGAT	10482
rs768783975	snp	C/G	8.23852e-05	0.00641762	intron-variant	NXF1	GRCh38.p7	11:62801867	CTAGGGAAGCCTAAG[C/G]CGCAAGAACAAGACC	10482
rs768785086	snp	C/T	3.29897e-05	0.00406125	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794960	TAGCAGGAACAGCAA[C/T]GAATGTCCGGGTGAA	10482
rs768831480	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62798119	GGTAACAGAGCAAGA[C/T]TCCATCCAAAAAAAA	10482
rs768833476	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795088	AATCATGGTCTTTGA[C/T]ATAAAGAATCCTAGC	10482
rs768917028	snp	A/G	1.64743e-05	0.00287	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796519	GGCCCCATCATGGTA[A/G]GCATCCAGGAGCCCT	10482
rs768943832	snp	C/T	1.6804e-05	0.00289858	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62805329	AAGACCAGCACTTAC[C/T]GCTGTACGACTTCCC	10482
rs768947327	snp	A/C	1.69009e-05	0.00290692	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805387	AAGGGCGGGCTCAGG[A/C]GCTGGCCGCTACGCC	10482
rs769051631	snp	C/G	5.43257e-05	0.00521152	intron-variant	NXF1	GRCh38.p7	11:62804250	TAGAAATGTGAGACC[C/G]AAAAGTGTAACTGAA	10482
rs769086364	snp	C/T	1.64757e-05	0.00287012	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796127	GTTTTGGGCAACTCA[C/T]TGAGGAAGGCAACAA	10482
rs769144144	snp	C/T	0.000364474	0.0134946	intron-variant	NXF1	GRCh38.p7	11:62801421	GGGCCACCAAATCTT[C/T]AGGAAGCAGAAGGGA	10482
rs769186150	snp	A/G	1.64876e-05	0.00287116	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801175	CAGCCTGTACAGCCT[A/G]TTGTTGCTCAAGTTC	10482
rs769204531	snp	A/G	7.35483e-05	0.00606372	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791804	CGGGACACGGCTGCC[A/G]CAGCCATGGAAGCCC	10482
rs769225510	snp	C/G	1.68935e-05	0.00290628	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805399	AGGCGCTGGCCGCTA[C/G]GCCGGCAAACAACCT	10482
rs769256996	snp	A/G			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807097	CTTCACTCACAGGAA[A/G]GTGGGTAAGGGCATC	10482
rs769304391	snp	C/G	1.67508e-05	0.00289398	intron-variant	NXF1	GRCh38.p7	11:62797152	TCCCCCTCAACCTCG[C/G]GGTGGGGAGGGGGGA	10482
rs769307705	snp	C/T	1.64827e-05	0.00287073	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803882	ATACCAGAACCGCCT[C/T]TTCCAGACCTACGGT	10482
rs769464415	snp	C/G	1.64885e-05	0.00287123	intron-variant	NXF1	GRCh38.p7	11:62801321	TAATACTGGGCCAAA[C/G]GCCTTACCTCAGGGA	10482
rs769490397	snp	C/T	6.59141e-05	0.00574045	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798618	ATGCTTCAGAGCCAC[C/T]GTGCCTCCTGGGCTG	10482
rs769553812	snp	G/T	3.98748e-05	0.00446495	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791901	AGAGCAGCACATCCC[G/T]TTGCAGCGTCGTGCC	10482
rs769604121	in-del	-/GG	6.62943e-05	0.00575698	intron-variant	NXF1	GRCh38.p7	11:62795036	AGCAACAACACCTTA[-/GG]GTCACTAGTGCTTTA	10482
rs769634203	in-del	-/GTT	0.000383215	0.0138369	intron-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791646	GTCCCGCCACCCCAC[-/GTT]GTCACAGTGGGAAGC	10482
rs769648064	snp	A/G	4.96857e-05	0.00498401	intron-variant	NXF1	GRCh38.p7	11:62795870	TGGGGGTGGGACCAC[A/G]CTACAAACTCGGGAC	10482
rs769695374	snp	G/T	1.65375e-05	0.0028755	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803805	ACTATCGTACTCGGG[G/T]ACCATCCTGGGCATC	10482
rs769797501	snp	A/C	1.64749e-05	0.00287005	intron-variant	NXF1	GRCh38.p7	11:62801713	GTAAGACTGGGTTGG[A/C]AACATCTAATTTGAG	10482
rs769807809	snp	A/T	3.36519e-05	0.00410181	intron-variant	NXF1	GRCh38.p7	11:62805320	CCCGACCCGAAGACC[A/T]GCACTTACCGCTGTA	10482
rs769876008	snp	A/G	1.64735e-05	0.00286993	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792439	TAATATCCAAGGACT[A/G]TTTACAGGGGGGACT	10482
rs769881060	snp	C/T	0.000139169	0.00834058	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791991	GCCTCCAAGGCGCCG[C/T]CATGGCCAGCCGACT	10482
rs769991733	snp	G/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806832	TCTGGTACTGGGCAG[G/T]GGGCTCTCTCCACTC	10482
rs770112022	snp	A/G	1.64773e-05	0.00287026	intron-variant	NXF1	GRCh38.p7	11:62796268	CTTTTCCCATATTTT[A/G]TTCGTATCACACACT	10482
rs770171593	snp	G/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793246	GCCAAGCCCCGCTAA[G/T]TTTTGTATTTTTAGT	10482
rs770209480	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62803185	TTAGCCGGGCGTGGT[C/G]GTGGGTGTCTGTAGT	10482
rs770220072	snp	A/C	4.39938e-05	0.00468988	intron-variant	NXF1	GRCh38.p7	11:62800508	AGGGTGGAAGGAACA[A/C]AGGGAGGAGACCCTG	10482
rs770325027	snp	C/G	0.000344768	0.013125	intron-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791655	CCCCACGTTGTCACA[C/G]TGGGAAGCCAGCCCA	10482
rs770344812	snp	A/G	4.94279e-05	0.00497107	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796154	ACAACGTTGAGACGC[A/G]TGTGCTTCAGCAGCC	10482
rs770405176	snp	A/G	1.64738e-05	0.00286995	intron-variant	NXF1	GRCh38.p7	11:62796352	AAGCTGCTTCTGGGG[A/G]AATAAAAGGAATGGA	10482
rs770427997	in-del	-/GTCACTGGGTTT	3.29468e-05	0.00405861	intron-variant	NXF1	GRCh38.p7	11:62801657	AAGAAGGGTTTAGTG[-/GTCACTGGGTTT]GTGTGTGGGGGGTGG	10482
rs770482309	snp	A/C	3.29788e-05	0.00406058	intron-variant	NXF1	GRCh38.p7	11:62801316	ATGCCTAATACTGGG[A/C]CAAAGGCCTTACCTC	10482
rs770608519	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797788	GTAGACTGAAGAACT[A/G]AGAGAGAAGGGTCAG	10482
rs770637882	in-del	-/AGAG			intron-variant	NXF1	GRCh38.p7	11:62804219	GTAGAAACTGGAATT[-/AGAG]AGAAGCAGGATGTAG	10482
rs770700366	snp	A/G	4.97253e-05	0.004986	intron-variant	NXF1	GRCh38.p7	11:62794917	ACTGGTATCCAATGC[A/G]AAAAGCAGAATACTT	10482
rs770749656	snp	A/G	6.86742e-05	0.00585939	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791812	GGCTGCCACAGCCAT[A/G]GAAGCCCAGAAGACG	10482
rs770769357	snp	C/T	1.64741e-05	0.00286998	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62798564	AACTTGGGAAATCGT[C/T]CGCGAATGGCGCTGT	10482
rs770786498	snp	A/G			missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803889	AACCGCCTCTTCCAG[A/G]CCTACGGTTTCCTTC	10482
rs770860085	snp	A/G	3.29478e-05	0.00405867	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794357	GGGCTGGAGGAAGGC[A/G]TGGGTGCAGGCATAG	10482
rs770879308	snp	A/T	5.36697e-05	0.00517996	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791956	GGGCCGCAGCACGGC[A/T]AGCAGCCCCGTGGGC	10482
rs770933831	snp	C/G/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792945	TGGTAGGGAAAGATG[C/G/T]TCATGGTGTAAGTAA	10482
rs770935982	snp	C/T	3.88372e-05	0.00440648	intron-variant	NXF1	GRCh38.p7	11:62804058	TAGCTTCTAGTACTC[C/T]GAACTATTGGAAGAG	10482
rs770990237	snp	A/G	1.64757e-05	0.00287012	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796144	GAGGAAGGCAACAAC[A/G]TTGAGACGCGTGTGC	10482
rs771024505	snp	G/T	1.65707e-05	0.00287838	intron-variant	NXF1	GRCh38.p7	11:62796048	CTAGGCTTCTGTCAG[G/T]CGCAAGCAGGAGCTT	10482
rs771059806	snp	C/G/T	0.000121175	0.00778287	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791988	ATCGCCTCCAAGGCG[C/G/T]CGCCATGGCCAGCCG	10482
rs771197620	snp	A/C			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806725	TTGCAACACTTGGTT[A/C]TCCCCTGCCTAGAGG	10482
rs771240463	snp	G/T	1.67624e-05	0.00289498	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794208	GCCCTCATTATTTAC[G/T]ACTAGCCCTACTTCA	10482
rs771244159	snp	A/G	4.12856e-05	0.00454325	intron-variant	NXF1	GRCh38.p7	11:62800498	TCAACTGCAAAGGGT[A/G]GAAGGAACAAAGGGA	10482
rs771354458	snp	C/G	9.92654e-05	0.00704435	intron-variant	NXF1	GRCh38.p7	11:62802157	TGCCTGGCCAGCCAG[C/G]CACTCAGGCCTTGTC	10482
rs771453318	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804881	AAGAACTAACACCCA[A/G]TGTAGTGTTCAGACT	10482
rs771480030	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793934	TGAACCCGGGAGGCA[A/G]AGGTTACAATGAGCC	10482
rs771489130	snp	A/C	3.3543e-05	0.00409516	upstream-variant-2KB, utr-variant-3-prime, missense	NXF1, STX5	GRCh38.p7	11:62807483	TTCAAGCAAGGAAGA[A/C]CACAAAGATGATGAA	10482
rs771496546	snp	C/T	0.000131036	0.00809325	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791711	ACGGCCAGACCGTAG[C/T]GCCAGAGCGCGGAGC	10482
rs771562384	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797460	ATCCCAGAACTTTGG[A/G]AGGCCGAGGCAGGCA	10482
rs771606778	in-del	-/T	1.64955e-05	0.00287184	intron-variant	NXF1	GRCh38.p7	11:62801291	CTATCTAACACACCC[-/T]TGCTTCCTCATGCCT	10482
rs771725816	snp	G/T	1.66416e-05	0.00288453	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794235	TTCAGTGCATCCCCA[G/T]CCTACACATGCCCCG	10482
rs771792879	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62802964	ACCTGCTCTAAGGTG[C/T]TGGAAGATACTGATT	10482
rs771864832	in-del	-/GAGTAGAGAG	1.72133e-05	0.00293366	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807456	CAACAGAGTGCCTCA[-/GAGTAGAGAG]GGTTCAAGCAAGGAA	10482
rs771928920	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801587	ACGGAGGCCTTTGAG[A/G]TCAAGGGCTTGTTGG	10482
rs771929912	snp	A/T	1.67267e-05	0.0028919	intron-variant	NXF1	GRCh38.p7	11:62804028	AGTAACTGGTCCGGT[A/T]TGGTGTGGCAATCAT	10482
rs771984852	snp	A/G	5.14284e-05	0.00507066	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791954	AGGGGCCGCAGCACG[A/G]CTAGCAGCCCCGTGG	10482
rs771987190	snp	C/G			upstream-variant-2KB	NXF1	GRCh38.p7	11:62805575	TTAAGGCCGTCGTTC[C/G]AGGGGCGGGGCCTGG	10482
rs772039708	snp	C/T	0.000101087	0.00710867	stop-gained, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791981	GTGGGCCATCGCCTC[C/T]AAGGCGCCGCCATGG	10482
rs772047653	snp	A/G	1.64727e-05	0.00286986	intron-variant	NXF1	GRCh38.p7	11:62801680	GTTTGTGTGTGGGGG[A/G]TGGGGGTGTGAGAAG	10482
rs772063402	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62797271	TTAGGAACATGGAAG[C/T]AGTATTCTCTCCACA	10482
rs772076964	snp	C/T			missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791687	GTCTTACCGATGGCG[C/T]CGCAGCCGACGGCCA	10482
rs772099017	snp	C/T	1.6495e-05	0.0028718	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62795918	TCCTTGAAGACTCCA[C/T]TGACAGAAAAACACA	10482
rs772149198	snp	A/G	1.64885e-05	0.00287123	stop-gained, nc-transcript-variant	NXF1	GRCh38.p7	11:62800399	AGGTGGACTGGTCTC[A/G]GAAGGTGTCACACAG	10482
rs772152309	snp	C/T	1.66153e-05	0.00288225	intron-variant	NXF1	GRCh38.p7	11:62796020	CCTATTAAATGCCAC[C/T]CCCACCCCAATTCTA	10482
rs772160863	snp	A/T	3.92372e-05	0.00442912	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800319	TGGTCAGGATGCATT[A/T]GCTCAGCCTCCCAGG	10482
rs772236957	snp	A/G	8.24015e-05	0.00641825	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803919	CACCATATTTCCACC[A/G]GAAGGGACCCCGGCC	10482
rs772387689	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802004	CAGAGGCAGTACTGG[C/T]GTCTTCAACGAAGAA	10482
rs772396623	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804427	GAGCTCTTCGTTTCC[A/G]TGGCCAGAAATGTCC	10482
rs772481948	snp	C/G			intron-variant	NXF1	GRCh38.p7	11:62804584	TCTTAAAAAAGGTCC[C/G]TAACTCCCAAAAGAG	10482
rs772511818	snp	A/C/T	0.000287046	0.0119768	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805396	CTCAGGCGCTGGCCG[A/C/T]TACGCCGGCAAACAA	10482
rs772587259	in-del	-/T	1.64806e-05	0.00287054	splice-acceptor-variant	NXF1	GRCh38.p7	11:62796183	CCGGAACCGCAAGGC[-/T]GTGGGTAGAGGAGAA	10482
rs772680652	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803555	CCCCGACGGTTAGGT[C/T]GGGTGGTATAGGGGT	10482
rs772740911	snp	A/C	1.67959e-05	0.00289787	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62805336	GCACTTACCGCTGTA[A/C]GACTTCCCCTCGTCC	10482
rs772747775	snp	C/G	2.28068e-05	0.00337682	intron-variant	NXF1	GRCh38.p7	11:62800514	GAAGGAACAAAGGGA[C/G]GAGACCCTGGTGAAG	10482
rs772898269	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795430	GCAGTGAGCCAAGAT[C/T]GCGCCACTGCACTCC	10482
rs772910560	snp	C/G	1.65051e-05	0.00287267	intron-variant	NXF1	GRCh38.p7	11:62803391	CCTCCTATCTCTACT[C/G]TACCATCTACTTTCT	10482
rs772929830	snp	C/T	1.66394e-05	0.00288434	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794237	CAGTGCATCCCCATC[C/T]TACACATGCCCCGCA	10482
rs773029566	snp	C/G	1.64738e-05	0.00286995	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794348	GTGGGCACCGGGCTG[C/G]AGGAAGGCGTGGGTG	10482
rs773135870	snp	C/T	1.64743e-05	0.00287	intron-variant	NXF1	GRCh38.p7	11:62797287	AGTATTCTCTCCACA[C/T]ACAAGTTCTTACTCT	10482
rs773136750	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800225	TGGAAGACACAGACA[C/G]ACCAAAGTGGGGAGC	10482
rs773148474	snp	C/G/T	4.94575e-05	0.00497259	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803923	ATATTTCCACCGGAA[C/G/T]GGACCCCGGCCTTTC	10482
rs773165414	snp	A/T	5.12125e-05	0.00506	intron-variant	NXF1	GRCh38.p7	11:62804032	ACTGGTCCGGTTTGG[A/T]GTGGCAATCATAGCT	10482
rs773212525	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801590	GAGGCCTTTGAGGTC[A/G]AGGGCTTGTTGGGAG	10482
rs773276470	snp	G/T	3.90801e-05	0.00442024	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791919	GCAGCGTCGTGCCTT[G/T]CAGGGGCCGGCAGGT	10482
rs773297777	snp	C/G	1.66272e-05	0.00288328	intron-variant	NXF1	GRCh38.p7	11:62797170	TGGGGAGGGGGGACC[C/G]TGGGATACTTACTGT	10482
rs773310489	snp	A/C	1.64887e-05	0.00287125	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800412	TCGGAAGGTGTCACA[A/C]AGGGAGTTTCCATCG	10482
rs773382511	snp	A/G	0.00011318	0.00752177	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791729	CAGAGCGCGGAGCGC[A/G]GGTCGAAGGGGCCAC	10482
rs773419793	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62804453	TGTCCTTTAACTCAG[A/G]AGACAAATTCTAGAC	10482
rs773487200	snp	C/T	1.64936e-05	0.00287168	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62795922	TGAAGACTCCATTGA[C/T]AGAAAAACACAGCAA	10482
rs773571173	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804651	CTCAACAAATGACCC[C/T]AGGAAAAAAGAACAT	10482
rs773792631	snp	C/G	1.68009e-05	0.00289831	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62805351	CGACTTCCCCTCGTC[C/G]GCCATGCCACAGCGA	10482
rs773882748	snp	C/T	1.72024e-05	0.00293273	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792750	TCTGACTCGTAAATG[C/T]CAGCTGAAAGTCCAC	10482
rs773891539	snp	C/T	6.60764e-05	0.00574751	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62802182	CTTGTCTTACCTCAA[C/T]AGGGGTGAAGGGCAC	10482
rs773899986	snp	C/T	1.67192e-05	0.00289125	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794222	CTACTAGCCCTACTT[C/T]AGTGCATCCCCATCC	10482
rs773917166	snp	A/T	1.64757e-05	0.00287012	intron-variant	NXF1	GRCh38.p7	11:62801904	CTGCTCTGAGCACCA[A/T]CCTCCACCTCCAGCC	10482
rs774048190	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62801519	TCCCTGACAGATCCC[A/G]CCTTATCACCACCTA	10482
rs774052877	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800091	GGAGATGCCTTTCCT[C/G]GAACAACAGGGTAGG	10482
rs774058169	snp	A/T	1.64751e-05	0.00287007	intron-variant	NXF1	GRCh38.p7	11:62797276	AACATGGAAGCAGTA[A/T]TCTCTCCACACACAA	10482
rs774165841	in-del	-/C	0.104938	0.20361	intron-variant	NXF1	GRCh38.p7	11:62795995	CTCAGAGCCTGAGTG[-/C]CCCCCCTTGCCTATT	10482
rs774256739	snp	A/G	4.99239e-05	0.00499594	intron-variant	NXF1	GRCh38.p7	11:62801444	AGAAGGGAAGGAAAG[A/G]GAAGACTGAGAGGGT	10482
rs774411059	snp	A/G	2.35408e-05	0.00343072	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800300	CATCTCCGCAGACGG[A/G]CCCTGGTCAGGATGC	10482
rs774412727	snp	C/T	1.64953e-05	0.00287182	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62794964	AGGAACAGCAATGAA[C/T]GTCCGGGTGAAGGCT	10482
rs774461949	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62803240	AGAATAGCTTGAACC[C/T]GGGAGGCGGAGGCTG	10482
rs774463524	snp	C/G	1.64991e-05	0.00287215	splice-donor-variant	NXF1	GRCh38.p7	11:62795900	CTCTAAAGATTCTTA[C/G]CTTCCTTGAAGACTC	10482
rs774489495	snp	C/T	3.29717e-05	0.00406015	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801349	GGATGTTCTCTTCAA[C/T]GATCCTCAGGGTAGC	10482
rs774531618	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62804261	GACCCAAAAGTGTAA[A/C]TGAACACAAATCAGA	10482
rs774538331	snp	C/T	0.000132164	0.008128	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801400	TCAGGACAACGTCAA[C/T]GTTCTGGGCCACCAA	10482
rs774673205	snp	C/G	3.29761e-05	0.00406041	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801178	CCTGTACAGCCTGTT[C/G]TTGCTCAAGTTCAAG	10482
rs774758326	snp	G/T	0.000134375	0.00819569	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62805332	ACCAGCACTTACCGC[G/T]GTACGACTTCCCCTC	10482
rs774789438	snp	A/C/T	3.42538e-05	0.00413835	intron-variant	NXF1	GRCh38.p7	11:62805279	CCTAGGCCGGCGCCG[A/C/T]CCACCCGCGCCCCAG	10482
rs774934118	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62795259	GAGGTGGGCAGATCA[C/T]GAGGTCAAGAGATCG	10482
rs774955090	snp	A/G	1.64876e-05	0.00287116	intron-variant	NXF1	GRCh38.p7	11:62801322	AATACTGGGCCAAAG[A/G]CCTTACCTCAGGGAT	10482
rs774980391	snp	A/G	6.68338e-05	0.00578035	intron-variant	NXF1	GRCh38.p7	11:62797157	CTCAACCTCGGGGTG[A/G]GGAGGGGGGACCCTG	10482
rs775036935	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797463	CCAGAACTTTGGGAG[A/G]CCGAGGCAGGCAGAT	10482
rs775115710	snp	A/C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798659	AAATATACCAAACCC[A/C/G]AGGGACAGCCCATCC	10482
rs775116482	snp	C/T	1.6525e-05	0.00287441	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803811	GTACTCGGGGACCAT[C/T]CTGGGCATCACTCAT	10482
rs775134070	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799858	GGCCTCAACCTCAGC[A/G]TGGACAGCAACAGCC	10482
rs775143077	in-del	-/G			frameshift-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791790	CCGGAACCGGGGGCC[-/G]GGACACGGCTGCCAC	10482
rs775347437	snp	A/G	5.66845e-05	0.00532344	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791837	AAGACGCCCTGGCCC[A/G]CGCAGAACAGCCCGA	10482
rs775359481	snp	C/T	1.64738e-05	0.00286995	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62798579	TCGCGAATGGCGCTG[C/T]CAAGAACGGGACAGA	10482
rs775402734	in-del	-/T			intron-variant	NXF1	GRCh38.p7	11:62795887	ACAAACTCGGGACTC[-/T]TAAAGATTCTTACCT	10482
rs775425544	snp	A/G	1.64789e-05	0.0028704	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797381	TGGGGGTAGCTCATG[A/G]CCATCCTGTGGAAAG	10482
rs775505140	snp	C/T	1.65064e-05	0.00287279	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794941	AATACTTACCCTGAA[C/T]TGCTAGCAGGAACAG	10482
rs775518535	snp	A/G	1.64754e-05	0.00287009	intron-variant	NXF1	GRCh38.p7	11:62801839	AGGGAAGACACAGAG[A/G]GCACAGAAAACTCTA	10482
rs775518908	in-del	-/AG			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806333	TGGAATGTATGAGAC[-/AG]GGGCACTCGAGTGAC	10482
rs775700748	snp	A/C	1.64741e-05	0.00286998	intron-variant	NXF1	GRCh38.p7	11:62801715	AAGACTGGGTTGGAA[A/C]CATCTAATTTGAGCC	10482
rs775740118	snp	C/G	0.000176165	0.00938357	intron-variant	NXF1	GRCh38.p7	11:62804220	TAGAAACTGGAATTA[C/G]AGAGAAGCAGGATGT	10482
rs775757468	snp	A/G	4.94205e-05	0.0049707	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801962	GGTTCTCCCGATCCA[A/G]AATCTTATAGTTGAC	10482
rs775789558	snp	C/T			upstream-variant-2KB	NXF1	GRCh38.p7	11:62805950	TAATTAAGGGCTTTT[C/T]TTCCTCGAGGGCTTG	10482
rs775809135	snp	A/G	2.2456e-05	0.00335075	intron-variant	NXF1	GRCh38.p7	11:62804071	TCTGAACTATTGGAA[A/G]AGATACATACTAACG	10482
rs775820343	snp	A/G	0.000132144	0.0081274	intron-variant	NXF1	GRCh38.p7	11:62803372	ATCTCCACTCTCAGC[A/G]TGGCCTCCTATCTCT	10482
rs775875742	snp	C/T	3.29462e-05	0.00405857	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792440	AATATCCAAGGACTA[C/T]TTACAGGGGGGACTG	10482
rs775877324	in-del	-/G	3.29468e-05	0.00405861	intron-variant	NXF1	GRCh38.p7	11:62801674	ACTGGGTTTGTGTGT[-/G]GGGGGGTGGGGGTGT	10482
rs775960515	snp	C/T			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793267	TATTTTTAGTAGAGA[C/T]GAGATTTCACCATGT	10482
rs775996249	snp	C/T	1.64787e-05	0.00287038	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796174	CTTCAGCAGCCGGAA[C/T]CGCAAGGCTGTGGGT	10482
rs776091267	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806838	ACTGGGCAGTGGGCT[C/T]TCTCCACTCGCTGCC	10482
rs776109645	snp	A/G	4.94629e-05	0.00497283	intron-variant	NXF1	GRCh38.p7	11:62801319	CCTAATACTGGGCCA[A/G]AGGCCTTACCTCAGG	10482
rs776113292	snp	C/G	3.29473e-05	0.00405864	intron-variant	NXF1	GRCh38.p7	11:62796366	GGAATAAAAGGAATG[C/G]ACGTGGTGTTCAGAG	10482
rs776158090	snp	A/G	1.6489e-05	0.00287128	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796073	GAGCTTACTGTCTGG[A/G]CGCTTATGTCTACCA	10482
rs776166593	snp	C/T	1.65078e-05	0.00287291	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796544	AGCCCTTGTCGGTCT[C/T]CAGAGTCGTAAATTG	10482
rs776278080	snp	A/G	1.65018e-05	0.00287239	intron-variant	NXF1	GRCh38.p7	11:62801208	GGACAATAGCTGTGA[A/G]GAGAGAAGAGTTTAG	10482
rs776371107	snp	C/T	1.94972e-05	0.00312221	intron-variant	NXF1	GRCh38.p7	11:62796610	GGGCTCTGTGGTCTA[C/T]AGCCATACAAGGACC	10482
rs776381984	snp	C/G	3.29478e-05	0.00405867	intron-variant	NXF1	GRCh38.p7	11:62797301	ACACAAGTTCTTACT[C/G]TGTCCATGCTTCCTA	10482
rs776458158	snp	A/G	6.69053e-05	0.00578344	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791816	GCCACAGCCATGGAA[A/G]CCCAGAAGACGCCCT	10482
rs776462307	snp	A/G	1.64901e-05	0.00287137	intron-variant	NXF1	GRCh38.p7	11:62803411	ATCTACTTTCTCAAA[A/G]TACTCACTGTAATCT	10482
rs776538505	snp	A/G	1.6473e-05	0.00286988	stop-gained, nc-transcript-variant	NXF1	GRCh38.p7	11:62801616	GGGAGCCATCGTATC[A/G]TTTGCTCATGATCAG	10482
rs776551711	snp	C/G	3.29478e-05	0.00405867	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794359	GCTGGAGGAAGGCGT[C/G]GGTGCAGGCATAGCG	10482
rs776582183	snp	C/G	1.6476e-05	0.00287014	intron-variant	NXF1	GRCh38.p7	11:62801698	GGGGTGTGAGAAGTA[C/G]TAAGACTGGGTTGGA	10482
rs776658958	snp	C/T	0.00112994	0.0237423	intron-variant	NXF1	GRCh38.p7	11:62804179	AAAGTTACTGGAAAA[C/T]TGTGTAGGGCTTTTG	10482
rs776700782	snp	G/T			intron-variant	NXF1	GRCh38.p7	11:62803124	AGGAGTTCGAGACCA[G/T]CCTGGCCAATACAGT	10482
rs776746957	snp	A/G	1.64757e-05	0.00287012	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796147	GAAGGCAACAACGTT[A/G]AGACGCGTGTGCTTC	10482
rs776826474	snp	A/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806736	GGTTCTCCCCTGCCT[A/T]GAGGCAGCTGTGTGT	10482
rs776938603	snp	A/G	0.00010895	0.00737992	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791957	GGCCGCAGCACGGCT[A/G]GCAGCCCCGTGGGCC	10482
rs777153637	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804540	CTCCAGGAAGATGAC[C/T]TTCTGATTCATGCTG	10482
rs777207617	snp	A/C/T	1.68134e-05	0.00289938	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791808	ACACGGCTGCCACAG[A/C/T]CATGGAAGCCCAGAA	10482
rs777274771	snp	A/T			intron-variant	NXF1	GRCh38.p7	11:62803730	GGAAATGACATGGAC[A/T]GTAAAAGGGCCATAT	10482
rs777290047	snp	G/T	1.65334e-05	0.00287514	intron-variant	NXF1	GRCh38.p7	11:62802161	TGGCCAGCCAGCCAC[G/T]CAGGCCTTGTCTTAC	10482
rs777313914	in-del	-/GAT	1.67363e-05	0.00289272	upstream-variant-2KB, cds-indel	NXF1, STX5	GRCh38.p7	11:62807490	AAGGAAGACCACAAA[-/GAT]GATGAAGAAGACAAT	10482
rs777422844	snp	G/T	1.64738e-05	0.00286995	intron-variant	NXF1	GRCh38.p7	11:62801682	TTGTGTGTGGGGGGT[G/T]GGGGTGTGAGAAGTA	10482
rs777490497	snp	A/G	2.08201e-05	0.00322639	upstream-variant-2KB, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62792036	TCCTGCCGCAGAGCC[A/G]CCTTCCGCCCTCCCT	10482
rs777581042	snp	A/G	1.97591e-05	0.00314312	intron-variant	NXF1	GRCh38.p7	11:62804154	CTCTGTGGGAGGGCA[A/G]CATCAGGGAAAAGTT	10482
rs777591405	snp	A/C	1.64806e-05	0.00287054	intron-variant	NXF1	GRCh38.p7	11:62796251	TGATTCCTTCCCATG[A/C]CCTTTTCCCATATTT	10482
rs777598606	snp	C/T	3.29495e-05	0.00405877	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62798545	TGGACTTACCAGGCG[C/T]AGTAACTTGGGAAAT	10482
rs777618216	snp	C/G	1.69115e-05	0.00290782	intron-variant	NXF1	GRCh38.p7	11:62805306	CCAGATAGCCAGTTC[C/G]CGACCCGAAGACCAG	10482
rs777667612	snp	A/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801798	TGTGGGGTGGAGCAG[A/T]AGAGTTGATGATGAT	10482
rs777738730	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800221	AAGCTGGAAGACACA[A/G]ACAGACCAAAGTGGG	10482
rs777758009	snp	C/T	1.64749e-05	0.00287005	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62797366	ATCAAAGGCAATTGG[C/T]GGGGGTAGCTCATGG	10482
rs777868807	snp	C/T			upstream-variant-2KB, downstream-variant-500B	NXF1, STX5	GRCh38.p7	11:62806581	AGAATTACGGCCAAA[C/T]AGTTGGAGGATACAG	10482
rs777946270	snp	G/T	1.6476e-05	0.00287014	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796116	CGTCGTGCTGGGTTT[G/T]GGGCAACTCATTGAG	10482
rs778004065	in-del	-/A	1.68818e-05	0.00290527	upstream-variant-2KB, intron-variant, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792745	AGAACTCTGACTCGT[-/A]AATGCCAGCTGAAAG	10482
rs778062340	snp	A/C	6.91491e-05	0.00587961	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792812	ATGTACATTCTTATA[A/C]ATCCTTGCACTATTT	10482
rs778088036	snp	C/G/T	0.000314337	0.0125333	intron-variant	NXF1	GRCh38.p7	11:62802156	GTGCCTGGCCAGCCA[C/G/T]CCACTCAGGCCTTGT	10482
rs778245562	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799362	TCTCTGTCTGCTACC[C/T]GGGTCCCGATCTGAA	10482
rs778249365	snp	G/T	3.40426e-05	0.00412554	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807465	GCCTCAGAGTAGAGA[G/T]GGTTCAAGCAAGGAA	10482
rs778282605	snp	A/G	3.29484e-05	0.00405871	intron-variant	NXF1	GRCh38.p7	11:62801530	TCCCACCTTATCACC[A/G]CCTATCTGAGAACTA	10482
rs778328082	snp	C/T	1.64757e-05	0.00287012	utr-variant-3-prime, missense, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794321	AACATTTCCTGCTGC[C/T]CTGGAGAGAGGGTGG	10482
rs778445025	snp	A/G	3.29587e-05	0.00405934	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62803572	GGTGGTATAGGGGTT[A/G]CTGTGGGTAAGCAGA	10482
rs778524648	snp	C/G	1.64811e-05	0.00287059	intron-variant	NXF1	GRCh38.p7	11:62798516	ATGCTGTGCTTGTTA[C/G]AATGAAAAAATTATG	10482
rs778664263	snp	C/T	1.72299e-05	0.00293508	intron-variant	NXF1	GRCh38.p7	11:62804118	TGCAAACTCCGCTCC[C/T]TATCCACAGGAAAGA	10482
rs778780752	in-del	-/GGAG	1.65124e-05	0.00287331	intron-variant	NXF1	GRCh38.p7	11:62801225	AGAGAAGAGTTTAGA[-/GGAG]GCACCACCAGCAAGT	10482
rs778823631	snp	A/C	1.67013e-05	0.0028897	intron-variant	NXF1	GRCh38.p7	11:62804016	AAATTAGAAGTAAGT[A/C]ACTGGTCCGGTTTGG	10482
rs778827238	snp	A/G	1.74239e-05	0.00295155	stop-gained, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791976	GCCCCGTGGGCCATC[A/G]CCTCCAAGGCGCCGC	10482
rs778851087	snp	A/G	5.35671e-05	0.00517501	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62800474	TCTTGTCCAATTCCC[A/G]CTCAGACTTCAACTG	10482
rs778854752	snp	A/G	3.29886e-05	0.00406118	intron-variant	NXF1	GRCh38.p7	11:62795990	CACTTCTCAGAGCCT[A/G]AGTGCCCCCCCTTGC	10482
rs778903527	in-del	-/C	1.70966e-05	0.0029237	intron-variant	NXF1	GRCh38.p7	11:62805287	GGCGCCGCCCACCCG[-/C]GCCCCAGATAGCCAG	10482
rs778917278	snp	C/T			intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794506	CCAACATCATTCCTA[C/T]TCTCTGATTCTTTCA	10482
rs778965926	snp	A/G	1.69069e-05	0.00290743	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805388	AGGGCGGGCTCAGGC[A/G]CTGGCCGCTACGCCG	10482
rs778982704	snp	C/T	2.30412e-05	0.00339412	upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792788	AAGCACCCAAGTTTG[C/T]CAACAAATATGTACA	10482
rs779014618	snp	A/G	1.64882e-05	0.00287121	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62800394	GATGTAGGTGGACTG[A/G]TCTCGGAAGGTGTCA	10482
rs779021026	snp	C/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801993	AGCCTTCAATGCAGA[C/G]GCAGTACTGGCGTCT	10482
rs779024930	snp	C/G	1.64803e-05	0.00287052	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792701	GTTGTCCTGAAGGCA[C/G]CTGGAGTGGAAGAAC	10482
rs779050001	snp	C/T	1.65842e-05	0.00287955	intron-variant	NXF1	GRCh38.p7	11:62802132	CAGCTTGCCCCTTCA[C/T]CATCCCTGGTGCCTG	10482
rs779185154	snp	A/C	1.67775e-05	0.00289629	intron-variant	NXF1	GRCh38.p7	11:62797139	GTCTGCCCACCATTC[A/C]CCCTCAACCTCGGGG	10482
rs779212958	snp	C/T	1.73869e-05	0.00294842	upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807449	CAAACCCCAACAGAG[C/T]GCCTCAGAGTAGAGA	10482
rs779231858	snp	A/T	3.30426e-05	0.0040645	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801399	TTCAGGACAACGTCA[A/T]TGTTCTGGGCCACCA	10482
rs779265214	snp	A/G			intron-variant	NXF1	GRCh38.p7	11:62797806	AGAGAAGGGTCAGAA[A/G]TCAAGTGTAAACGCA	10482
rs779322858	snp	C/G	1.64749e-05	0.00287005	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62796528	ATGGTAGGCATCCAG[C/G]AGCCCTTGTCGGTCT	10482
rs779393008	snp	A/G	3.29728e-05	0.00406021	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803865	CAAGGCGGGAAGACC[A/G]AATACCAGAACCGCC	10482
rs779426873	snp	A/C	1.6473e-05	0.00286988	intron-variant	NXF1	GRCh38.p7	11:62801556	AACTACTGCTGTCAA[A/C]CATACCTGGGTCTGA	10482
rs779446750	snp	C/T	4.40403e-05	0.00469235	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791883	GGCCCCGATCATGCT[C/T]AAAGAGCAGCACATC	10482
rs779477225	snp	C/T	0.00013192	0.00812049	intron-variant	NXF1	GRCh38.p7	11:62801304	CCCTGCTTCCTCATG[C/T]CTAATACTGGGCCAA	10482
rs779483904	snp	C/T	1.6476e-05	0.00287014	intron-variant	NXF1	GRCh38.p7	11:62797263	AACAGGTATTAGGAA[C/T]ATGGAAGCAGTATTC	10482
rs779498267	snp	A/C			upstream-variant-2KB	NXF1	GRCh38.p7	11:62806263	GGGCTCTCCTAGACC[A/C]CCAAAAGCACCACCA	10482
rs779561338	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	NXF1, STX5	GRCh38.p7	11:62807131	TCCCTTTGCTGCCAA[C/T]GCTTCCTTTGGGAGA	10482
rs779663983	snp	C/T	0.000148252	0.00860837	intron-variant	NXF1	GRCh38.p7	11:62801662	GGGTTTAGTGGTCAC[C/T]GGGTTTGTGTGTGGG	10482
rs779733290	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804327	TTTGTCTATACAGTG[C/T]AGACGCCAGTTACAA	10482
rs779773460	snp	A/G			upstream-variant-2KB, intron-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62793104	TTTTTTTTTGAGACC[A/G]AGTCTTGCTCTGTCA	10482
rs779784734	snp	A/G	8.58517e-05	0.00655122	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791942	CGGCAGGTGAGCAGG[A/G]GCCGCAGCACGGCTA	10482
rs779811948	snp	C/G	1.65748e-05	0.00287874	synonymous-codon, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800358	GTCCCCAGGAGGGGA[C/G]ACACAGGCTACAACT	10482
rs779814469	snp	C/T	1.64817e-05	0.00287064	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803894	CCTCTTCCAGACCTA[C/T]GGTTTCCTTCACCAT	10482
rs779844064	snp	G/T			utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805442	CTCAGGACCGAAGTG[G/T]CCCTACGCCGGGCGC	10482
rs779849727	snp	A/G			upstream-variant-2KB, intron-variant, downstream-variant-500B	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792575	TCAGCAACCCCACTC[A/G]GCTAACCTGACCTCC	10482
rs779885007	in-del	-/A	3.29598e-05	0.00405941	intron-variant	NXF1	GRCh38.p7	11:62798521	GTGCTTGTTAGAATG[-/A]AAAAATTATGGACTT	10482
rs779918280	snp	A/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801975	CAAAATCTTATAGTT[A/G]ACAGCCTTCAATGCA	10482
rs780115078	snp	C/T			utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62794992	GCTCGCAAAGAATCC[C/T]GGGACTTTCCGTCCA	10482
rs780120981	in-del	-/AAGT	0.000133413	0.00816633	intron-variant	NXF1	GRCh38.p7	11:62804008	AGGAACACAAATTAG[-/AAGT]AAGTAACTGGTCCGG	10482
rs780153226	snp	A/G	1.68638e-05	0.00290373	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805380	GAAGATCAAGGGCGG[A/G]CTCAGGCGCTGGCCG	10482
rs780199704	snp	C/G	1.68252e-05	0.0029004	intron-variant	NXF1	GRCh38.p7	11:62805321	CCGACCCGAAGACCA[C/G]CACTTACCGCTGTAC	10482
rs780326943	snp	C/T	9.88549e-05	0.00702977	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796101	CCACGAAGGAATTGA[C/T]GTCGTGCTGGGTTTT	10482
rs780456957	snp	A/C	1.6473e-05	0.00286988	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62796490	GGAATGAAAGGAATG[A/C]TCAGGGAACAGCAGG	10482
rs780466346	snp	C/T	3.2969e-05	0.00405998	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801147	CCTTCTGAACAATGC[C/T]AGACATGTCATCCAG	10482
rs780616193	snp	C/T	1.6477e-05	0.00287024	intron-variant	NXF1	GRCh38.p7	11:62796271	TTCCCATATTTTGTT[C/T]GTATCACACACTTAC	10482
rs780633627	snp	A/G	1.68715e-05	0.00290439	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794476	AAAAAGCTAGACAGA[A/G]ATAACATCATCCTCC	10482
rs780728532	snp	C/T	1.65446e-05	0.00287612	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801409	CGTCAATGTTCTGGG[C/T]CACCAAATCTTCAGG	10482
rs780777962	snp	A/G	4.16363e-05	0.0045625	synonymous-codon, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791892	CATGCTCAAAGAGCA[A/G]CACATCCCGTTGCAG	10482
rs780833651	snp	C/T	3.29478e-05	0.00405867	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62798565	ACTTGGGAAATCGTT[C/T]GCGAATGGCGCTGTC	10482
rs780907762	snp	A/C	1.6661e-05	0.00288621	intron-variant	NXF1	GRCh38.p7	11:62803785	ACCAGACCAACTGGT[A/C]ACTCACTATCGTACT	10482
rs780994986	snp	A/G	3.295e-05	0.00405881	synonymous-codon, nc-transcript-variant	NXF1	GRCh38.p7	11:62801808	AGCAGAAGAGTTGAT[A/G]ATGATAGATATCTGG	10482
rs781019689	snp	A/G	1.64727e-05	0.00286986	upstream-variant-2KB, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant	TMEM223, NXF1, MIR6514	GRCh38.p7	11:62792492	CACTTCATGAATGCC[A/G]CTTCTGGGATCTCGC	10482
rs781026286	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62801956	CCCTTCGGTTCTCCC[A/G]ATCCAAAATCTTATA	10482
rs781057620	snp	C/G/T	3.36617e-05	0.00410243	intron-variant	NXF1	GRCh38.p7	11:62805319	TCCCGACCCGAAGAC[C/G/T]AGCACTTACCGCTGT	10482
rs781066803	in-del	-/AGACAG	5.03926e-05	0.00501934	intron-variant, upstream-variant-2KB	NXF1, MIR6514	GRCh38.p7	11:62794469	AGCACTTAAAAAGCT[-/AGACAG]AGATAACATCATCCT	10482
rs781077548	snp	C/T	2.65523e-05	0.00364355	utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62800273	GACAGGTGGTTCCAG[C/T]TCAGGGCTGCACATC	10482
rs781096992	snp	C/T			utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805412	TACGCCGGCAAACAA[C/T]CTAACTCCCAAGCGC	10482
rs781112412	snp	C/T	3.36536e-05	0.00410191	utr-variant-5-prime, nc-transcript-variant	NXF1	GRCh38.p7	11:62805371	TGCCACAGCGAAGAT[C/T]AAGGGCGGGCTCAGG	10482
rs781224393	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62803511	TCCGCACAGTAACAT[A/G]AATGCGATCTCGATC	10482
rs781295120	snp	C/T			intron-variant	NXF1	GRCh38.p7	11:62804050	GGCAATCATAGCTTC[C/T]AGTACTCTGAACTAT	10482
rs781322345	snp	C/T	3.29554e-05	0.00405914	intron-variant	NXF1	GRCh38.p7	11:62796260	CCCATGCCCTTTTCC[C/T]ATATTTTGTTCGTAT	10482
rs781359312	snp	C/G	8.06809e-05	0.0063509	missense, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791796	CCGGGGGCCGGGACA[C/G]GGCTGCCACAGCCAT	10482
rs781391430	in-del	-/A	4.94181e-05	0.00497057	intron-variant	NXF1	GRCh38.p7	11:62797297	CACACACAAGTTCTT[-/A]ACTCTGTCCATGCTT	10482
rs781480219	snp	A/G	1.64966e-05	0.00287194	utr-variant-3-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	NXF1, MIR6514	GRCh38.p7	11:62794275	CTGGGACCACTCGAG[A/G]TTCATGCCAGACTGG	10482
rs781592249	snp	A/G	0.000375587	0.0136986	intron-variant, downstream-variant-500B	TMEM223, NXF1	GRCh38.p7	11:62791646	GTCCCGCCACCCCAC[A/G]TTGTCACAGTGGGAA	10482
rs781685575	snp	G/T	1.87862e-05	0.00306476	intron-variant	NXF1	GRCh38.p7	11:62802295	AAAAGAAGGGAATGA[G/T]AAGTAAGGCTGAATA	10482
rs781712060	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	NXF1	GRCh38.p7	11:62799445	TGTGAGGGTTCAGGC[C/T]CCTGTAGGATTGTGG	10482
rs781722278	snp	A/G	4.27433e-05	0.00462275	intron-variant	NXF1	GRCh38.p7	11:62800503	TGCAAAGGGTGGAAG[A/G]AACAAAGGGAGGAGA	10482
rs781740092	snp	A/G	3.29451e-05	0.00405851	utr-variant-3-prime, missense, nc-transcript-variant	NXF1	GRCh38.p7	11:62797334	TTGCAGGGCGGTAAC[A/G]TCGTGGGGGCTTCAA	10482
rs796650057	snp	A/C			intron-variant	NXF1	GRCh38.p7	11:62797875	GCTCACACCTGTAAT[A/C]CCAGCACACTGGGAG	10482

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