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

NUP153

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs145075461	in-del	-/CA			intron-variant	NUP153	GRCh38.p7	6:17673046	GAATACACACACACG[-/CA]CACACACACACAAAA	9972
rs145085663	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17692172	CTGGAAAACATAACT[A/G]GTCAAAGTGGATATA	9972
rs145118618	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652172	CTCCCTCCCCATGAA[A/T]AATGAATAAGAACAA	9972
rs145147755	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17625080	CCACACCTTTACAGC[C/T]GACAATTTCTGGTAA	9972
rs145165971	snp	C/T	6.58989e-05	0.00573978	missense	NUP153	GRCh38.p7	6:17624725	CCAAAGCCTGGGGGA[C/T]TGGGCTGGCTGGCAC	9972
rs145203588	snp	C/G	4.94385e-05	0.0049716	missense	NUP153	GRCh38.p7	6:17675626	AGGGAAAATCCCGAA[C/G]TGCCAATTGGGAATG	9972
rs145212163	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655566	TCAAGCGATTCTTCT[A/G]CCTCAGCTTCCCGAG	9972
rs145241480	snp	C/T	1.65899e-05	0.00288005	intron-variant	NUP153	GRCh38.p7	6:17661624	GCTTTTTAAATAAAC[C/T]TCAAGAGTATATGAG	9972
rs145273505	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619869	TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG	9972
rs145277962	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17659770	GCCACCGTGCCCAGC[C/T]GCCAACCCGTTTCTT	9972
rs145291906	snp	G/T	0.000362671	0.0134612	synonymous-codon	NUP153	GRCh38.p7	6:17626022	AGGATTGCTGGACTG[G/T]CCAAACACAAAGGTA	9972
rs145299685	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619126	ACAATTCCAGAAAGA[A/G]GAAACAGGCCAAAGA	9972
rs145299953	snp	A/G	6.59044e-05	0.00574002	missense	NUP153	GRCh38.p7	6:17616164	CCAGAAGAAGAGAAC[A/G]CATTTTTCCCATTTG	9972
rs145353495	snp	C/T	0.0170251	0.090679	intron-variant	NUP153	GRCh38.p7	6:17702980	CTGTGGCGGGTGGAT[C/T]ACCTGAGGTCAGGAG	9972
rs145402823	snp	C/T	0.182296	0.240658	intron-variant	NUP153	GRCh38.p7	6:17667452	AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9972
rs145431834	in-del	-/AAAG			intron-variant	NUP153	GRCh38.p7	6:17686154	TCTTGTCTTTAAAAA[-/AAAG]AAAGAAAGAAAGAAA	9972
rs145527673	snp	A/C	1.64846e-05	0.0028709	missense	NUP153	GRCh38.p7	6:17675577	GATGTTATCATCATC[A/C]TGCTGAGAGGTAGAA	9972
rs145528364	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673681	ACATGCCTACTAGAA[C/T]AGCAAAAACAAACAA	9972
rs145528681	snp	G/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17683510	GTGTTGTTTTGCAAA[G/T]AATCTTTTTGTCCCC	9972
rs145537391	snp	C/T	8.2373e-05	0.00641714	missense	NUP153	GRCh38.p7	6:17661696	AAGCGTGTTCTTTCT[C/T]GTCTCATCTTGCCAC	9972
rs145574658	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648355	GGAGTGGGGGCTCAC[A/G]CTTGTAATCCTAGCA	9972
rs145609362	in-del	-/TTTG	0.0330485	0.124226	intron-variant	NUP153	GRCh38.p7	6:17616746	AAAATGATAGGTTTT[-/TTTG]TTTGTTTGTTTGTTT	9972
rs145622778	snp	A/G	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17678760	ACCAGCCTGGGCAAC[A/G]TACTGAGACTTCATC	9972
rs145635881	snp	C/G	6.58935e-05	0.00573955	missense	NUP153	GRCh38.p7	6:17624695	GGAAATAATGCTGTG[C/G]AAGATGATATAGATC	9972
rs145660844	in-del	-/AAAAAAAC			intron-variant	NUP153	GRCh38.p7	6:17679786	GTCACAAAAAGAAAA[-/AAAAAAAC]CAGCCATTCTTCGGT	9972
rs145716827	snp	C/G	3.29451e-05	0.00405851	missense	NUP153	GRCh38.p7	6:17637405	CACATTTTATTGCTT[C/G]AGGTTTATTTTGCAC	9972
rs145739236	snp	A/G/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17624399	GTCTGTGAAACCTGC[A/G/T]AATGTTGTTTATATA	9972
rs145759780	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17695055	GACCCAAATACAGGC[A/G]TGTCCTTGGATCATG	9972
rs145845474	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631345	CAAAGTAGATAAAGC[C/T]TGCTATTATTTTTGT	9972
rs145861696	snp	A/T	0.00676609	0.0577691	intron-variant	NUP153	GRCh38.p7	6:17630252	AGAGATTGAACCTTG[A/T]CACAATTTCTTGATT	9972
rs145899695	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621102	CACACAAATGGCCAA[C/T]AGACCTGAAAAAATG	9972
rs145901655	snp	C/T	0.0142736	0.0832652	intron-variant	NUP153	GRCh38.p7	6:17667347	TCAATATCTTAGTCA[C/T]TGCAATTAATTCATA	9972
rs145903629	snp	A/C	0.0267878	0.112589	intron-variant	NUP153	GRCh38.p7	6:17703152	GCAGTGAGCCAAGAT[A/C]GAGCCACTGCACTCC	9972
rs145977467	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17691142	GCAAAAGCGAGACTC[C/T]GTCTCAAGAAAAAAA	9972
rs145995066	snp	C/T	0.0252325	0.109451	intron-variant	NUP153	GRCh38.p7	6:17676365	TTCCCAGAGTCTTTA[C/T]TCCTCTCTTCCTCTA	9972
rs146021515	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635806	CATCAAAAATACAAA[C/T]TTGACTGTATCACTC	9972
rs146088300	snp	C/T	0.0217236	0.101931	intron-variant	NUP153	GRCh38.p7	6:17702462	GCAGTGAGCAGAGAT[C/T]GTGCCACTGCACTCC	9972
rs146106733	snp	A/G	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17636603	TGAGTTAAAGATTCA[A/G]TATGAATCTTCACTA	9972
rs146115099	snp	G/T	0.0170251	0.090679	intron-variant	NUP153	GRCh38.p7	6:17621748	ACAAACATATAGCTA[G/T]ATAGAAGGAATAAAT	9972
rs146127316	snp	A/G	0.0182019	0.0936463	intron-variant	NUP153	GRCh38.p7	6:17694066	TCCACCTACTTTATT[A/G]ATAGCACTGAATCAC	9972
rs146284308	snp	C/T	0.000164777	0.00907532	missense	NUP153	GRCh38.p7	6:17637669	TCTCCCCAAACCCAA[C/T]TCCACTAGAAGAAAA	9972
rs146309521	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705188	AACAGTAGGCAACAA[A/G]TTATCAGATCCTTTT	9972
rs146343288	snp	C/G	0.0275645	0.114116	intron-variant	NUP153	GRCh38.p7	6:17689625	CACCACAACCTCCGC[C/G]TCCTGGGTTCAATGG	9972
rs146346677	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671244	TGTCTATAATTCATG[A/G]GAAATAATAGTCTGT	9972
rs146359181	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614977	TGTTAATCTTTATTT[C/T]ACAAAGTCCCCCCAA	9972
rs146385070	snp	A/G	0.00953873	0.0683987	intron-variant	NUP153	GRCh38.p7	6:17618275	TTAAGTGGTATTTAC[A/G]TGTCCTACACTCATA	9972
rs146424102	snp	A/T	0.0111196	0.0737302	intron-variant	NUP153	GRCh38.p7	6:17684097	CTCTGCCTTCTGCCA[A/T]GAGTAAAACCTTGAG	9972
rs146439339	snp	A/C/G	9.89828e-05	0.00703439	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616060	GAAAGCAGGGCACCA[A/C/G]CTGTTGTTAAAATTG	9972
rs146486464	in-del	-/GAACCCGGGTGGCGTAGCTTGCAGTGA	0.195214	0.243923	intron-variant	NUP153	GRCh38.p7	6:17690270	GCAGGAGAATGGCGT[-/GAACCCGGGTGGCGTAGCTTGCAGTGA]GAACCCGGGTGGCGT	9972
rs146495938	snp	C/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17648911	ATCTTACTGGAAACA[C/T]TATTTGGAAACAAAT	9972
rs146527993	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17680827	CACTGTTGTTGGTGG[A/G]AATTATCAATTAGTA	9972
rs146547596	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17699324	ACATGGTGAAACCCC[A/G]TCCCTACTAAAGATA	9972
rs146551209	snp	A/C/G	0.000197682	0.00994003	missense	NUP153	GRCh38.p7	6:17629041	GCACTCTTGGTTTCT[A/C/G]TGGTTCCAAGGTTGA	9972
rs146566870	snp	C/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17652960	CTTGAACCCACGAGG[C/T]GGAGGTTGCAGTGAG	9972
rs146590928	snp	A/T	1.64904e-05	0.00287139	missense	NUP153	GRCh38.p7	6:17637199	ATTGTCTTCTGCATT[A/T]TTAGAAACACAGCAT	9972
rs146628588	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17646414	GGTTTCACTGTGTTA[A/G]CCAGGATGGTCTCGA	9972
rs146672699	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17647427	AAAACAGCAATTAAA[A/G]GACAGTCTGGGGATA	9972
rs146683760	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17651751	ATCACTATGGAGCCA[C/T]AGAATAAATGTAAAG	9972
rs146755187	snp	C/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17684515	GATCTTCTATCTAAA[C/G]CAACTCAAACTTTCT	9972
rs146765927	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687798	TAAATTGGGCTTCAT[C/T]GAAATTTAAAACACG	9972
rs146794318	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17666412	CCCGGCTATTCAGGA[G/T]GCTGAGGCAGGAGAA	9972
rs146804964	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17669937	CCATCTGTATTAAAA[C/T]ACAAAAAATTAGCCA	9972
rs146889233	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662195	TTTAGTTAATGAATC[A/C]TGAAATTTGAAATTA	9972
rs146889301	snp	C/T	0.0197687	0.0974348	intron-variant	NUP153	GRCh38.p7	6:17702637	GCCGAGATTGCACCA[C/T]TGCACTCCAGCCTGG	9972
rs146910093	in-del	-/AT	0.168135	0.236216	intron-variant	NUP153	GRCh38.p7	6:17633125	CTCCCCCTTAACCAC[-/AT]GTTTGAACTGCTGTG	9972
rs146935030	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704144	AAAAATACAAAAAAT[C/T]AGCTGGGCGTGGTGG	9972
rs146944202	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707625	GTCAGCTAACATTAG[C/G]GGTAAGTGATATATC	9972
rs146944577	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668478	CCAAAAAAAAATTGG[A/G]TGAGTATCTACTACA	9972
rs146947469	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17668374	GTAAGCCACCGCACC[-/C]TGGCCGATCACTCCT	9972
rs146952318	snp	A/G	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17637527	TTATTTGGTGTTTCA[A/G]TTCCAGTCTGTTTAG	9972
rs146967613	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670812	ATCCCATTAATTTTT[A/T]ATTTTTTATTTTTTT	9972
rs147050757	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685265	ATAAGAACAGTCAAC[C/T]AGTTGGGAGCGGTGG	9972
rs147055009	in-del	-/A/AAAAAA			intron-variant	NUP153	GRCh38.p7	6:17699481	GGCGAGACTCGTCTC[-/A/AAAAAA]CAAAAAAAAAAAAAA	9972
rs147064942	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617317	AACAAGGGATTTTTA[C/T]AAAGATATAGGTTTA	9972
rs147073289	snp	G/T	0.0225045	0.103662	intron-variant	NUP153	GRCh38.p7	6:17689089	AAAAAAAAAATACAG[G/T]AACTAAAACAATCTG	9972
rs147136905	snp	C/T	0.000477948	0.0154514	intron-variant	NUP153	GRCh38.p7	6:17626191	AAATTAAGAAACAAA[C/T]ATAAATCCTTAAGAA	9972
rs147207748	snp	C/T	0.0205511	0.0992634	intron-variant	NUP153	GRCh38.p7	6:17664945	GTAGTCCCAGCTACT[C/T]GGGGGGCTGAAGCAG	9972
rs147231802	snp	A/C	0.0248432	0.108648	intron-variant	NUP153	GRCh38.p7	6:17623042	GGCTGAGGCAGAAGA[A/C]TCACTTGAACCCGGG	9972
rs147233505	snp	C/T	3.35458e-05	0.00409534	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706281	GGGTCCCATACCTGA[C/T]GCTGTTGTCGCCCCT	9972
rs147337838	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17642652	AAAAGTTTAATACAG[A/T]ACTACCATCTGACCC	9972
rs147338020	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17634992	AATAAAAAAAAAAAA[A/T]AAATCGCAAAAGAAT	9972
rs147340353	snp	C/G	1.64806e-05	0.00287054	missense	NUP153	GRCh38.p7	6:17625935	TGTGGTTGCTAGTTT[C/G]CTATCTTGAGAAAAT	9972
rs147420729	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698362	CTTTGGAGGCCAAGG[C/G]AGGGGTTCTGCTTCA	9972
rs147438534	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17659301	ATAAGCAAATTTATT[C/T]CTCGTTGGCAAAAAT	9972
rs147596923	snp	G/T	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17673747	CAGCAACTCTTATAT[G/T]ACCAGTCAGAATGAA	9972
rs147620438	snp	C/T	0.00795532	0.062565	intron-variant	NUP153	GRCh38.p7	6:17660579	ATACATATTTCTTAA[C/T]ATACATATAAGAAAT	9972
rs147630955	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619541	TCTTTCAGTGCTTAC[C/T]TCAGCAGCACATACC	9972
rs147681704	snp	A/C			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632336	AAAAAAACAAACAAA[A/C]AAAAAAACAAAGAAC	9972
rs147717188	snp	C/T	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637467	ACTGGTTTAAATTTG[C/T]CTCCAAAGCCTGTCC	9972
rs147725766	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17635055	GTTGAGCCTCATTCA[C/T]AGCCATCCTAAGCCA	9972
rs147753355	snp	C/T	0.00023062	0.0107358	missense	NUP153	GRCh38.p7	6:17647836	GTACATTTGCCTCAG[C/T]AGATTTTACGATTGG	9972
rs147829891	snp	C/T	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17694908	CGCTTGAACCCAGGA[C/T]GCAGAGGTTGCAGTG	9972
rs147839451	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17655133	AGCTTTTTAACAACA[C/G]ACACAAAAAAACTCA	9972
rs147912725	snp	C/T	0.039522	0.134904	intron-variant	NUP153	GRCh38.p7	6:17655578	TCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA	9972
rs147920879	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707558	ATGGAGAGCATGTAT[A/G]TTTGCTAATAGACGA	9972
rs147934136	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17643613	TGTTAGGATTCCCTA[A/G]AGTATGCTCAAAAAG	9972
rs147936475	snp	C/T	0.00031309	0.0125079	missense	NUP153	GRCh38.p7	6:17649188	AATGCTTGAGACGAA[C/T]TGATGGGTGATGGAG	9972
rs147957015	in-del	-/C	0.170408	0.236992	intron-variant	NUP153	GRCh38.p7	6:17655423	AGGCCCATGAAAATG[-/C]CGCCCCCACAAAAAT	9972
rs148025619	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17641344	GATGGAGACCATCCC[A/G]GCCAACATAGTGAAA	9972
rs148072993	in-del	-/ACAC			intron-variant	NUP153	GRCh38.p7	6:17663233	TAAAAAGAAAAAAAT[-/ACAC]ACACACACACACACA	9972
rs148087255	snp	A/C	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17656871	GGAGTAGCTGGAATG[A/C]AATGTGGAAATTTGG	9972
rs148131302	snp	C/T	0.0252325	0.109451	intron-variant	NUP153	GRCh38.p7	6:17701191	GATGGTGCCGTTGCA[C/T]TCCAGCCTGGGCAAC	9972
rs148150942	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17690395	AAAAAAAAAAGTATG[A/G]GCTTTGGGATTGCCA	9972
rs148190521	snp	C/G/T	6.59167e-05	0.00574061	synonymous-codon	NUP153	GRCh38.p7	6:17649262	TGAAGAACTGGTGAT[C/G/T]GGTAGAGAGATTTTC	9972
rs148228850	snp	G/T	0.000197726	0.00994102	synonymous-codon	NUP153	GRCh38.p7	6:17625887	GGCTCCTGGACCAAA[G/T]ACAAATGGGGTGACA	9972
rs148244190	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686157	TGTCTTTAAAAAAAA[A/G]AAAGAAAGAAAGAAA	9972
rs148245908	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17688452	TCAGTAATATTAGAG[C/T]TCTCCTCATCGGCAT	9972
rs148299988	snp	A/C	0.0387552	0.1337	intron-variant	NUP153	GRCh38.p7	6:17693666	CCGAGGCGGGCAGAT[A/C]ACTTGAAGTCAGGAG	9972
rs148303907	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620415	ACTCTCTTCAGTAAA[G/T]GGTGCTTGGAAAACT	9972
rs148351772	snp	A/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17625093	GCCGACAATTTCTGG[A/T]AAAGGAACATATCTC	9972
rs148383798	snp	C/T	0.00116914	0.0241496	missense	NUP153	GRCh38.p7	6:17629009	CTGATGTCTTACATG[C/T]GAAAGGAGCCACTGA	9972
rs148405683	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17622578	TTTCAACAACAGTGT[A/G]ACTCTAATTTTTAGG	9972
rs148414349	snp	A/C	0.0189856	0.0955633	intron-variant	NUP153	GRCh38.p7	6:17694427	ACTTCCGGAGGCCGA[A/C]GCGGGCGGATTACCT	9972
rs148425175	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17683528	TCTTTTTGTCCCCAA[A/G]CAAGAGGTCTCAACA	9972
rs148448624	snp	A/G	0.0130921	0.0798413	intron-variant	NUP153	GRCh38.p7	6:17669736	TTTACTGGAAATCCA[A/G]TTCTCTGATTGAGAA	9972
rs148457514	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627485	TTTGCCTTTGTGTTG[A/G]TGTTTTTTTGTTGTT	9972
rs148495824	snp	A/G	0.0271762	0.113356	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705865	AAACACACTAAAGAA[A/G]GGACACCAGAAAACA	9972
rs148502354	snp	C/G	1.74199e-05	0.00295121	missense, intron-variant	NUP153	GRCh38.p7	6:17668992	TTTCTCTTTTGGCCT[C/G]AAAATCTGTGATATC	9972
rs148580415	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649902	TCTTGGAACATATCC[C/T]TTGCAGATAAGGGGG	9972
rs148614370	snp	C/T	0.0225045	0.103662	intron-variant	NUP153	GRCh38.p7	6:17658950	CTTTCAGAATCCCAG[C/T]GAAACCACTACATCT	9972
rs148637207	snp	A/C/G	0.0182344	0.0939844	intron-variant	NUP153	GRCh38.p7	6:17618791	CAGGATGGTCTCGAT[A/C/G]TCCTGACCTCGTGAT	9972
rs148651242	snp	A/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17702202	TACCTATTCACTCTC[A/T]ACTAGAAAAATGACA	9972
rs148674375	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665830	CCTGTGTACACAGGC[A/G]TGCGCCACCACACCC	9972
rs148704532	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17672611	GACGGTGCAAAAGCT[A/G]TTCAATGAACAAAGA	9972
rs148791647	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17685940	CTCACTTGAGGCCAG[C/T]TGAAGCCCAGCCTAA	9972
rs148819564	snp	C/G	1.648e-05	0.0028705	missense	NUP153	GRCh38.p7	6:17675621	TTACAAGGGAAAATC[C/G]CGAACTGCCAATTGG	9972
rs148897027	snp	C/T	0.00953873	0.0683987	intron-variant	NUP153	GRCh38.p7	6:17616890	CAGTAGCTGGGACTA[C/T]ATAGGTGCGTGCCAC	9972
rs148936288	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17695279	CTCAGATCAGCAGCA[C/T]TGGTGTAGCCTATGA	9972
rs148973599	snp	C/T	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17643794	GACTCCTTAAAAATC[C/T]GGGTAACTTCCTGAG	9972
rs148989123	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700674	TATCACAAAGAAGCT[A/G]CCAAAACAAATAAAA	9972
rs148993544	snp	C/T	0.0383715	0.133092	intron-variant	NUP153	GRCh38.p7	6:17630400	CGTGGTAGCTCACGC[C/T]TGGAATCCCAGCACT	9972
rs148995292	snp	C/G	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17637417	CTTCAGGTTTATTTT[C/G]CACTAAACAGGTATC	9972
rs149022481	snp	A/G	0.000166911	0.00913389	intron-variant	NUP153	GRCh38.p7	6:17640067	GTGACATGATGAGCT[A/G]TAATTTTTTTAAATT	9972
rs149030321	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708093	CAAGCTATTCTCCTG[C/T]CTCGGCTTCCTAAGT	9972
rs149046438	snp	A/G	0.000115353	0.00759362	missense	NUP153	GRCh38.p7	6:17649194	TGAGACGAATTGATG[A/G]GTGATGGAGAGGAAG	9972
rs149096395	snp	C/T	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17616534	TCTCTTACCCCACTG[C/T]AAATGCTGCTGGAGA	9972
rs149098394	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17692195	TGGATATAATAAAGC[C/T]CACTCACTAAAATAC	9972
rs149107201	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17652318	ACATTTCAAAACACT[A/G]AAGTCATAATCTCAA	9972
rs149150045	snp	C/G/T	0.000385079	0.0138707	intron-variant	NUP153	GRCh38.p7	6:17661814	TTAAAACAACTGATA[C/G/T]ATTATTGTGGTCCAT	9972
rs149172885	in-del	-/AGG	0.174288	0.23826	intron-variant	NUP153	GRCh38.p7	6:17656111	TCAGGAGGCTGAGGC[-/AGG]AGAATTGCTTGAACT	9972
rs149181085	snp	G/T	0.0387552	0.1337	intron-variant	NUP153	GRCh38.p7	6:17703059	AAAAATTAGCCGGGC[G/T]TGGTGGCGCATGCCT	9972
rs149189847	in-del	-/C	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17684713	AAACTTACATACTTA[-/C]AGCTTTTGGATAAAA	9972
rs149256701	snp	A/G	0.0387552	0.1337	intron-variant	NUP153	GRCh38.p7	6:17635361	TGATCCACTCGCCTC[A/G]GCCTCCCAAAGTGCT	9972
rs149294986	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681262	ACAGAATAGAATGAC[A/G]AATACCAGTGGGCAA	9972
rs149307511	snp	A/G	4.94752e-05	0.00497344	synonymous-codon	NUP153	GRCh38.p7	6:17669511	GTAAGATTGTGCACT[A/G]AGTTGCTTAGCTTTC	9972
rs149312629	snp	A/T	8.23771e-05	0.0064173	missense	NUP153	GRCh38.p7	6:17637662	TTTAAACTCTCCCCA[A/T]ACCCAATTCCACTAG	9972
rs149374964	snp	C/T	0.00042905	0.0146404	synonymous-codon	NUP153	GRCh38.p7	6:17665374	CTGAACAGGAGGATA[C/T]TGAGAATCCACCTTA	9972
rs149382310	snp	A/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17685163	AAATTAATATTTAGT[A/T]AACAACTAAATTTAT	9972
rs149416399	snp	C/T	3.29549e-05	0.00405911	synonymous-codon	NUP153	GRCh38.p7	6:17625878	ATTACTGCTGGCTCC[C/T]GGACCAAAGACAAAT	9972
rs149434388	snp	C/T	0.00874735	0.0655527	intron-variant	NUP153	GRCh38.p7	6:17618089	AATGAAGTTCTCTGA[C/T]ACCCTCCATGCAGGA	9972
rs149467403	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17697395	TTAACCTGAGTTGAA[C/G]GATTAATGAGCTGGG	9972
rs149490078	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17658515	AATGGCCAGCCACTG[C/G]AAGTTGACAATAACC	9972
rs149500275	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17645267	AAAAAAAAAGAATTC[C/T]ATGTTTTAATTCTCT	9972
rs149527356	snp	A/G	0.0197687	0.0974348	intron-variant	NUP153	GRCh38.p7	6:17702020	GGTTTCCTCTCACCA[A/G]GAGGTGGCAGTAGGT	9972
rs149528825	in-del	-/AGTATTATTC	0.173965	0.238157	intron-variant	NUP153	GRCh38.p7	6:17681072	ACATATACACAATGG[-/AGTATTATTC]AGCCATTAAAAAAAA	9972
rs149646574	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654043	ATTTTTCTTTTTTGA[C/T]AAAGCAAATGTAACA	9972
rs149664123	snp	A/G	0.00488303	0.0491698	synonymous-codon	NUP153	GRCh38.p7	6:17616652	TGGACTGTTGTTTGT[A/G]AAGTTGAAATTTGTA	9972
rs149745966	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655082	TCTTATATACTGCTA[C/T]ATGTTTTGTATACTG	9972
rs149770475	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17677626	CACTGCTTTCCTACC[C/T]ACCTTTCCTTTGGTT	9972
rs149781715	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17636997	AACATAAAGATCTAG[C/T]TGCAAACAAGACATT	9972
rs149798900	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17624169	AAGTGTCATGAGACA[A/G]CTCAGCGGGACTGCC	9972
rs149809114	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17695022	GTACTATGGACTGAA[C/T]GAACAAAAAGGTGCT	9972
rs149824534	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17683323	AGGAATGACTATGAT[A/G]GCTATAGCCATATGA	9972
rs149844090	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670569	AGCACCTGCAGTATG[A/C]TGTTAAACAGTAGCA	9972
rs149960579	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17692166	AAACAACTGGAAAAC[A/G]TAACTGGTCAAAGTG	9972
rs149980354	snp	A/G	0.00953873	0.0683987	intron-variant	NUP153	GRCh38.p7	6:17641787	AACCTGAGAGGTGGA[A/G]CTTGCAGTGAAACGA	9972
rs150001516	snp	G/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17699314	AGCCTGGCCAACATG[G/T]TGAAACCCCGTCCCT	9972
rs150011571	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661503	GGTACTAGATTAGGT[C/T]TTCAGCATGCATTTT	9972
rs150060913	snp	A/G	0.000564613	0.0167925	missense	NUP153	GRCh38.p7	6:17646129	TCTGCTGTTTTTGCA[A/G]CAGGCACACTAAATG	9972
rs150079998	snp	A/G	1.64735e-05	0.00286993	missense	NUP153	GRCh38.p7	6:17637554	TTAGCAGTATCTCTG[A/G]GTGACAATTTTGCTG	9972
rs150124998	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17663378	ACGTGATCCTCCTAC[C/T]GCAACCTCCTGCCTT	9972
rs150238408	in-del	-/G	0.00154245	0.0277281	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706250	TTTCCCCACCCGCCA[-/G]GCCACCGCGGCGTCG	9972
rs150260928	in-del	-/GG			intron-variant	NUP153	GRCh38.p7	6:17701833	CAAGACTCTGTCTCG[-/GG]GGGGGGGGGGGAAAA	9972
rs150314375	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17639541	TGCTCCCTATGTATA[C/T]GTTACAATTCAGCAG	9972
rs150336462	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696350	GGAAGGCCCAATGTA[A/G]CCCACCTATGTTTTG	9972
rs150345386	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684797	AATTAGCCTAATTTC[A/C]ATACTGTCAGAGAAT	9972
rs150398806	snp	A/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17653036	GGCGGGTGGACTGCC[A/T]TAGCTCAGGAGTTTG	9972
rs150448927	snp	A/C/T	0.00445509	0.0469867	missense	NUP153	GRCh38.p7	6:17629053	TCTATGGTTCCAAGG[A/C/T]TGAAGCTGCTCTTGT	9972
rs150474474	snp	C/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17635004	AAATAAATCGCAAAA[C/G]AATCTCATAATGTTT	9972
rs150495519	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17693889	TCCCAAAGTGCACCA[A/C]CACCGCGCCTGGCCT	9972
rs150513300	snp	C/T	0.173965	0.238157	intron-variant	NUP153	GRCh38.p7	6:17654589	CCTCCGAAAGTGCTG[C/T]GATTACAGGCATGAA	9972
rs150577758	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704445	TCAAAGGCATTCATA[A/G]GAGAAAAGAAAGCAT	9972
rs150601952	snp	A/C/T	0.00181268	0.0300512	missense	NUP153	GRCh38.p7	6:17626050	GTAGCCACAGGTGGA[A/C/T]TGGAGGAAGAGGTGG	9972
rs150640243	in-del	-/A	0.0362652	0.129682	intron-variant	NUP153	GRCh38.p7	6:17672013	TCCCATCTAAAAAAT[-/A]AAAAAAAGCAATTCC	9972
rs150671485	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650124	ATAAACGTTTAGATA[C/T]ATGATAAACTCTGGA	9972
rs150756309	snp	A/C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625529	AGCAAGACTCCGTCT[A/C/T]GAAAGAAAACAAAAA	9972
rs150786193	snp	C/G	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17671100	TGAGCCACCACACCT[C/G]GTCTAATCCCATTAA	9972
rs150808282	snp	G/T	0.0256215	0.110247	intron-variant	NUP153	GRCh38.p7	6:17631823	ACACAAAAAATTAGC[G/T]AGGCGTGGTGGCAGG	9972
rs150839587	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17641712	CAAAACAAATTAGCC[A/G]GGCGTGGTGGCAGGC	9972
rs150847776	snp	A/G	0.00758236	0.061107	synonymous-codon	NUP153	GRCh38.p7	6:17688463	AGAGCTCTCCTCATC[A/G]GCATATACCAGATGG	9972
rs150896669	snp	C/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17690228	GTGGTGGCGGGCGCA[C/T]GTAGTCCCAGCTACT	9972
rs150955067	snp	A/G	0.0232847	0.105357	intron-variant	NUP153	GRCh38.p7	6:17644073	AAAAGATAAGGTTGC[A/G]AACATACCAGTCAAA	9972
rs150960390	in-del	-/AAAC	0.210069	0.24679	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632325	AACAAACAAACAAAA[-/AAAC]AAACAAACAAAAAAA	9972
rs150985275	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17688174	AATTAAAACCCAAAA[C/T]CCAACATCAGAGCTT	9972
rs151006799	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17648422	AGGAGTTCAAGATCA[A/G]CCTAACCAACATGGT	9972
rs151026767	snp	C/T	0.116138	0.211142	intron-variant	NUP153	GRCh38.p7	6:17695834	CTAACACGGTGAAAC[C/T]CTGTCTCTACTAAAA	9972
rs151069864	snp	A/G	0.0115144	0.0749975	intron-variant	NUP153	GRCh38.p7	6:17666054	GATCTCAAACTTCTG[A/G]GCTCAAGCAATCCTT	9972
rs151124118	snp	C/T	0.173965	0.238157	intron-variant	NUP153	GRCh38.p7	6:17670092	CAGAGCGAGACTCTT[C/T]CTCAAAAAAAAAAAA	9972
rs151167422	snp	C/T	0.00874735	0.0655527	intron-variant	NUP153	GRCh38.p7	6:17679848	GAATTCCAGGAATTG[C/T]TCTTAGGAGATCCAA	9972
rs151192201	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17657385	CGTCTCTACTAAAAT[-/A]AAAAAAATAAAAAAA	9972
rs151201054	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17652460	GAAATTAGAAAAACT[A/G]TAAAAGCAAAATTAC	9972
rs151286304	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17628208	CTCTTGTTTTCTCAG[A/G]ATTAATTATATTTGT	9972
rs151323191	snp	A/C	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17673152	CGCGGGTGAATCACA[A/C]GGTCAAGAGTTCGAG	9972
rs151333933	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634748	GGTCACATTACATAC[A/G]TCTGAATGTTGACTT	9972
rs180691234	snp	A/G	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17631343	TACAAAGTAGATAAA[A/G]CTTGCTATTATTTTT	9972
rs180708624	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17623055	GAATCACTTGAACCC[A/G]GGAAGCGGAGGTTGC	9972
rs180709952	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17664300	AACAACTCACAGACA[C/T]CACTTTATTTATAAA	9972
rs180711552	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649006	CAAGATATTTGTACA[A/T]TTTTTTAAAAAAGCA	9972
rs180724785	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17641253	ATAAGAAACAAGATG[C/T]GGCCAGGCACGGGGG	9972
rs180726969	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682384	CTGGGTTGGTTGTAG[C/G]AATTTCTTAAAATAA	9972
rs180806199	snp	C/G/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17673106	GGGCGCGGTGGCTCA[C/G/T]GCCTGTAATCCCAGC	9972
rs180808978	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690619	TGGGGTAAGGTAACC[A/G]ATTTTAGGCAACAAT	9972
rs180820100	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657688	TGTATTTTCCTCATA[C/G]AGAGATAAACTTCAC	9972
rs180849593	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697581	AATCCCAGCTACTTG[A/G]GAGGCTGAGGGAGGG	9972
rs180861906	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17694651	GACAGAGCAAGACTC[C/T]GTCTCACAAAAAAGA	9972
rs180921149	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653486	GATATAAAATGGCAC[A/G]CTTTAGAAAACAGTA	9972
rs180929655	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17667396	TTACTTTTGAGGAAC[C/T]TGGTATTCCAAGAAA	9972
rs180934108	snp	C/T	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17628223	GATTAATTATATTTG[C/T]TGTCTATGTTTCTTA	9972
rs180944309	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662446	AATTAATACTTCCAC[C/T]GAAAGGAATCAAGAC	9972
rs180948699	snp	C/T	0.0130921	0.0798413	intron-variant	NUP153	GRCh38.p7	6:17701622	GCCGAGGTCGCACCA[C/T]TGCACTCCAGCCTGG	9972
rs180974788	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17645317	TCTTTTTTTTTGAGA[A/T]AGGGTCTTGCTCTGT	9972
rs180992013	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17677428	GGGTAGGGGGTGGGG[A/G]AGAGTAGGTGTTAGA	9972
rs181278554	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17636200	ATTAGTTGGGTGTGG[C/T]GGCATGCACCTGTAA	9972
rs181279965	snp	C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17676708	AAAAAAACTCACAAG[C/G]TGAGCCCTACGATTA	9972
rs181282939	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17619863	AGCAGTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	9972
rs181297502	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694168	CCAAGAAGGCAGGAA[C/T]TTGTTCACTGCTGTA	9972
rs181298687	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654559	ATTCCTGACCTCGTG[A/G]TCCGCCCACCTCGGC	9972
rs181301909	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669927	TGGTGAAACCCCATC[A/T]GTATTAAAATACAAA	9972
rs181421869	snp	C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17702805	CTGTTCTTCATATTT[C/G]CTTCTACAATTCTTA	9972
rs181456416	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17644990	ACTCGGGAGGTTGAG[A/G]AGGAGAATGGCATGA	9972
rs181483450	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619225	TATAAAAATGATTTC[C/T]AATCTACATCTATAT	9972
rs181506389	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654290	AGGCACACACTTGTC[C/T]ACACTGGTTCCTTAT	9972
rs181507477	snp	A/G	0.000830247	0.0203577	intron-variant	NUP153	GRCh38.p7	6:17661790	AGCCACTGGCAAATA[A/G]AAAGAAAATTAAAAC	9972
rs181528841	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687942	ACACGGTGAAACCCC[A/G]TCTCTATAAAAAATA	9972
rs181582795	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695456	TAAGCTTAACTACAA[C/T]AGAATTTTACCTAAA	9972
rs181584823	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17640608	GAAATACTTATGCAG[C/T]CACAGAAATCATTCT	9972
rs181588350	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627206	AAGAATGGTTAAGAG[C/T]GTCTACCATAGCCTG	9972
rs181591936	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657151	ATTTATAGCTTAGTT[A/T]TGGCTGTCTTGCAGA	9972
rs181600899	snp	C/T	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17672771	ATTGCTTGAGCCCAG[C/T]AGTTCAGGATCAGCC	9972
rs181632001	snp	A/G	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17635179	CAGTGGCATGATCTC[A/G]GCTCACTGCAAGCTC	9972
rs181639931	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17667827	CCAAACTATCAAACA[C/T]TGTATTTTTTTCCCA	9972
rs181688037	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687189	TGAAGTTAGTTAATC[C/T]TTTCAAATATGCTCA	9972
rs181729689	snp	A/G	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17699443	AGCCGAAATCGCACC[A/G]TTGCACTTCAGCCTG	9972
rs181805225	snp	A/C	0.0178098	0.0926698	intron-variant	NUP153	GRCh38.p7	6:17702235	ATTTCTGGCCGGGCG[A/C]GGTAGCTCATGCCTG	9972
rs181816756	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17665620	TGGCTTCACGGATAC[A/T]CTATATTTCATTCCA	9972
rs181881985	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683498	TGTTAATGAGCAGTG[C/T]TGTTTTGCAAAGAAT	9972
rs181998324	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17649843	AAAAAACACAGTATA[C/T]ACAGGGTTCAATATT	9972
rs182011739	snp	C/T	0.00144471	0.0268378	intron-variant	NUP153	GRCh38.p7	6:17665226	AGACTGGTAGAAATA[C/T]ACATATACTCACACT	9972
rs182017195	snp	A/C	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17683035	ACATCTTCATACTCC[A/C]CTTCTAATTTTAGTT	9972
rs182029332	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698940	GTTACCTACAAGATA[C/G]TATCACACTTTTTCT	9972
rs182061579	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650598	TCAATAAAATTGATC[C/G]AAAAGCCCAAAGCAA	9972
rs182074372	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617313	AAACAACAAGGGATT[G/T]TTACAAAGATATAGG	9972
rs182076398	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708834	CTATCTCCACAATCA[A/G]ACTGCACAATTCAGG	9972
rs182085527	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17631987	AACACAAAAATCTGG[C/T]CTCCAGTTAGTTTAG	9972
rs182089576	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615756	TGAACGCTTATCAGC[A/G]CACATAATGGTGTAG	9972
rs182162021	snp	A/C/G	6.58968e-05	0.00573969	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632756	GTCCCAGCTTCCCTC[A/C/G]GGTTTCTTGAACTTT	9972
rs182179490	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665904	ATGTTGCTCAGGCTG[G/T]TCTCAAACTCCTGGG	9972
rs182182532	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17651312	TCTCAAAAAACAAAA[A/C]CAAAACCAATAAAAA	9972
rs182188376	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692038	GTTTAGCTACTAAAC[A/G]TATCAGAGATTCCTG	9972
rs182213155	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17671221	ACAAATATTTTTGTT[A/G]AGGTTTGTGTCTATA	9972
rs182214509	snp	C/T	1.6476e-05	0.00287014	missense	NUP153	GRCh38.p7	6:17688434	TCAGGTGTGATTCTC[C/T]CATCAGTAATATTAG	9972
rs182219097	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646584	TTATAATATTTCACT[A/C]TCTCTAAAAGTGAGA	9972
rs182220794	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17703044	CGTCTCTAAAAATAC[A/C]AAAATTAGCCGGGCG	9972
rs182315969	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17638779	TACACAAGACAGACT[A/G]TACACATTTGAGGCT	9972
rs182327895	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17618782	CGTGTTAGCCAGGAT[C/G]GTCTCGATATCCTGA	9972
rs182542939	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625621	CCAAGAGGTAAATAT[A/G]TTAAAGTTGAACACA	9972
rs182545133	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695590	CGACCTTCGAGTTGA[C/T]TTCCACCGTTAAAGA	9972
rs182560385	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17683859	AGTGTAGTCATCTGA[A/T]AGTTTAGATGTTTGT	9972
rs182564039	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622392	ATGGCTTGAGCCCAG[C/T]AGGTTGAGGCAGTAG	9972
rs182566008	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17688979	CAGTATGTTAAAACA[C/T]AAACAATACTTTCAA	9972
rs182569317	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658817	ACGATAACCGGTTAC[A/G]ACCAGCTCAGTGGTT	9972
rs182594975	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663722	AGGTTTTCAATAAAT[C/T]GAGTTGTTAGAAATG	9972
rs182600445	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656872	GAGTAGCTGGAATGA[A/G]ATGTGGAAATTTGGG	9972
rs182617052	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695926	AGGCAGGAGAATGGC[A/G]TGAACCCGGAAGGCG	9972
rs182664008	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17637072	CTCATCCTGAAACAT[C/T]TAAAACAAGGATTCT	9972
rs182824985	snp	C/T	0.0019964	0.0315312	intron-variant	NUP153	GRCh38.p7	6:17679218	ATACAAAAATCAACA[C/T]AAAAAAATGTGTTTC	9972
rs182830217	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17643208	CTGGACGCGGTGGCT[C/T]ACACCTGTAATCCCA	9972
rs182844240	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699915	ACTAAGATATCTGCC[C/T]TGTCAGGGACTTCCC	9972
rs182846815	snp	A/G	0.00914312	0.0669923	intron-variant	NUP153	GRCh38.p7	6:17674685	TAAGGCAGGAGAATC[A/G]CTTGAAACCAGGAGA	9972
rs182850248	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705049	GGCGTGAGCCAACGC[A/G]CCCGACCCAAATCTT	9972
rs182879172	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679667	TGGTGAGAGAGAACA[A/G]GAGGTGGGAGGTAGT	9972
rs182888514	snp	A/G	9.88468e-05	0.00702948	missense	NUP153	GRCh38.p7	6:17628909	CTTCCCAAAACAAAC[A/G]CTGAGGCAGATGGCA	9972
rs182933897	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620087	TGGGCAACAGAGCAA[A/G]ACACCATCAAAAAAA	9972
rs183002306	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645774	AATGAGACTTGCTTT[A/G]TAACTAACTTGTCAC	9972
rs183013685	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662690	AGTAGAGAATCCTCA[A/C]AGACACCACTTTATG	9972
rs183017762	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17678100	GTGGTTCACACCTGT[A/G]ATCCCAGCACTTTGG	9972
rs183042796	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17658126	CAAAGGAGGCTGGGC[A/G]TGATGGCTCACGCCT	9972
rs183046071	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643005	CAAGTTGACAGTTAG[C/T]TAGGGGGAAGGCAGA	9972
rs183057025	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674105	ACTAAACGTATATGA[C/T]ATTCTGGAAAGGCCA	9972
rs183061779	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17691580	GACCAGCCTGGCCAA[C/T]ATGGCAAAACCCCGT	9972
rs183117329	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625278	ACAGTGGCTCACACC[G/T]GTAATCTCAGCACTT	9972
rs183120233	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685953	AGTTGAAGCCCAGCC[C/T]AAGCAACAGAGTTTG	9972
rs183130396	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17700629	TCCAGCTATCAGATA[C/T]CAGGCAGGACATACT	9972
rs183377733	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17620341	CAGAAACAAATCCAC[A/G]TATTTACAGCCAACT	9972
rs183383690	snp	A/T	1.64768e-05	0.00287021	synonymous-codon	NUP153	GRCh38.p7	6:17629082	GTTCTCAGAGGTCAC[A/T]ATGGTGTTAGCAGGA	9972
rs183406840	snp	A/G	0.000217699	0.0104308	intron-variant	NUP153	GRCh38.p7	6:17651936	TTGTCTCTACAAATA[A/G]TTTTAAAAATTGGCG	9972
rs183407145	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663090	AGTTTCTGGGTTTGA[C/T]CACTGCTATGCATTA	9972
rs183418498	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17655540	CTCACTGCAACCTCC[A/C]CCTCCCAGGTTCAAG	9972
rs183431013	snp	A/C	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17688823	CTATATGCATACATA[A/C]GGCAATAATTGTCCC	9972
rs183522916	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632413	CTGAGGCTCAATGAC[A/C]CAAGAAATTTTTTTT	9972
rs183572377	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703884	ATCAAGATTTAAAAC[A/C]AAACTACACAGCCTG	9972
rs183630890	snp	A/G	5.12772e-05	0.0050632	synonymous-codon	NUP153	GRCh38.p7	6:17637766	TATCTTCGGCGATGC[A/G]AAACCTACAATGAAC	9972
rs183654502	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671466	ACGTATTTTAAATTA[C/T]GAACTCAATTCACTG	9972
rs183704802	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652928	CAGCTACTAGGGAGA[C/T]TGAGGTAGGAGAATC	9972
rs183707948	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666975	TGTAGACTGTTCTGA[C/T]AACATCTGTGAAACA	9972
rs183710641	snp	G/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17686612	ATGTTAGCCAGGATG[G/T]TCTCAATCTCCTGAC	9972
rs183770080	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17634828	CAGTTCGATCAGTAC[A/G]TTATCTATTGCCTGT	9972
rs183774289	snp	A/C/G	0.011531	0.0752148	intron-variant	NUP153	GRCh38.p7	6:17618773	GGGTTTCACCGTGTT[A/C/G]GCCAGGATGGTCTCG	9972
rs183838934	snp	C/T	0.0113265	0.0743973	intron-variant	NUP153	GRCh38.p7	6:17672013	ATCCCATCTAAAAAA[C/T]AAAAAAAGCAATTCC	9972
rs183931559	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689464	GAAACAATCTAAAAT[A/C]TTTTCTGATGTTGAC	9972
rs183934591	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664738	TGCTAGAGTTTACTA[A/G]TCAACACTAACTTAA	9972
rs183944689	snp	A/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706914	GCGGCTGCCGCGGTC[A/G]CGAGCCAGAATGTCG	9972
rs184009845	snp	C/G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17641686	GTGAAACCCCGTTTC[C/G/T]ACTAAAAATACAAAA	9972
rs184017319	snp	A/C	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17655944	GCGCAGTGGTTCAAC[A/C]CTGCAATCCCAGCCC	9972
rs184034702	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617956	TGGACTGGGAGACAC[A/C]ACATACAGTTAAGGG	9972
rs184035380	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17671805	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	9972
rs184042642	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673446	AACATATAACAAAGT[A/G]TTTGTACCCTGAAAA	9972
rs184170799	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17623755	AGAGCAAAACAATCA[C/G]AAATCAAAAGACTGC	9972
rs184176913	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17633313	ATATGAATTTCAAGA[A/T]TTGAAAGCATAGATC	9972
rs184190657	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691185	AGGTAGCAACTGGGA[A/C]GCATGTAATTATTCT	9972
rs184253426	snp	A/C	0.0614824	0.164198	intron-variant	NUP153	GRCh38.p7	6:17663947	ACACACACAAACACA[A/C]AAAAAAACACTTATA	9972
rs184257735	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680623	TAAAAACTTTTATGC[A/G]TCAAAGAATGTAATC	9972
rs184258834	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622529	TTGTTATAGAACTGA[C/G]AACCTCAACCCTAAA	9972
rs184270245	snp	C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17696474	AAGATTTAAAAACAA[C/G]GCCAGGCACGGTGGC	9972
rs184297496	snp	A/G	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17637944	TATCAATTACCTAAT[A/G]AGTTACACTTAAACC	9972
rs184305837	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621716	GTGGTGGTAGGAAGG[C/G]AAGGTGGTTAACGAA	9972
rs184315709	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17630518	TACAAAAAAAATCAG[C/T]CAGGCATGGTGGTCT	9972
rs184332426	snp	C/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17648341	ATATTTTTTGGCCAG[C/G]AGTGGGGGCTCACGC	9972
rs184359370	snp	A/C	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17627095	CTCTCAGTTCCAATA[A/C]CGCACACTATCCAGG	9972
rs184374657	snp	A/G	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17661081	GCACTTTGCAAGGCC[A/G]AGGCAGGTGGATCAC	9972
rs184379059	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17644814	CCAGGGGCAGGGCGC[A/G]GTGGTTCACGCCTGT	9972
rs184385495	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17638385	CACACAACACCACCA[A/T]CTGTGATCTGTTTCT	9972
rs184401811	snp	C/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17701574	GGCTGAGGCAGAGAA[C/G]TGCTTGAACCCAGGA	9972
rs184474831	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676182	TTTCAATATGTCTAA[A/T]CTTGACTCCCATCTG	9972
rs184478035	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693702	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCAGC	9972
rs184492841	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17622299	TACAAACCACGCCCC[A/C]CTCCAAAAATGAAAC	9972
rs184520484	snp	C/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17656564	TATTTTTTTGTACAC[C/G]TGGGGTTTTGCCATG	9972
rs184525522	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698092	ATCTTTAACTATAAA[C/T]ATCAAATGCAGTCCA	9972
rs184565322	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643512	CCACCACTCGTACAA[C/T]TATGCCAAAACAAAC	9972
rs184569292	snp	C/G	0.0185938	0.0946107	intron-variant	NUP153	GRCh38.p7	6:17626365	CATCTTCTTTTATAG[C/G]TTATGGATTTTAGGC	9972
rs184637674	snp	C/G	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17681391	GGAGATCGAGACCAT[C/G]CTGGCTAACAGGTGA	9972
rs184657984	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17682691	CGGGAGGCTGAGGGG[G/T]GCAGATCACTAGGTC	9972
rs184727480	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686892	CAGCCGGGGGCGGGC[A/G]GCGGGGGAGGGGGGC	9972
rs184733251	snp	A/T	0.0256215	0.110247	intron-variant	NUP153	GRCh38.p7	6:17701676	AAAAAAAAAAAAAAA[A/T]TACAAAAATTAGCTA	9972
rs184753182	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631036	ACAGCTACAGAAAGA[C/G]ATAAAATGAACCAGA	9972
rs184779224	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664230	ATTTTCAAAGGGTGG[A/G]AGAGATGGTAATACA	9972
rs184788699	snp	A/G	0.0126979	0.078662	intron-variant	NUP153	GRCh38.p7	6:17696712	GTGAGCCAAGATGGC[A/G]CCACTGCACTCCAAC	9972
rs185010304	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636255	CACAAGAATTGCATG[C/T]ATCTGGGAGATGGAG	9972
rs185018546	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619938	CCCCGTCTCTACTAA[A/T]AATACAAAAATTAGC	9972
rs185020419	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654744	AACTTGATGCTTAGA[C/G]ACATCTCAAGTAGAA	9972
rs185095599	snp	A/C	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17656942	GGTCATATTAGTTCC[A/C]GCCAATTTCAGTCAG	9972
rs185102332	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17689993	TATCCCCACCTTATG[A/G]ATAAGACAAACAATG	9972
rs185194753	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634112	GGTTCATGAACCCCC[A/C]CCATTACTCCCACCA	9972
rs185205145	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17666861	GCAGCTGTGAACAAC[A/T]TTGGTTTCCAGGGCA	9972
rs185215268	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672353	GAAGCCAACACAGGA[A/G]GATCGCTTGAGCCCA	9972
rs185225515	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708136	AGGCGTGCACCACCA[C/T]GCCCAGCTGATTTGT	9972
rs185266342	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690861	ATGTGAAAAGGTAGC[C/T]GGGCGTGGTGGCTCA	9972
rs185268537	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672874	TGACCAATACCTCAT[A/G]CCACACACAAAAATC	9972
rs185284873	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17690245	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	9972
rs185290407	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17618615	CTGTTGCCCAGGCTG[C/G]AGTGCAGTGGCACGG	9972
rs185316532	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17652523	TTTGTAGCCCGGGGA[C/T]AGGCAAAATTTTCTT	9972
rs185319701	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701296	GCACTTTGAGAGGCC[A/G]AGGAGGCCAGACCAC	9972
rs185324361	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686273	AGCTCCATGGATGTT[A/G]ATGCCCCTGAAGAGT	9972
rs185337432	snp	G/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614651	GGGGGGGGGGGGGAG[G/T]GCAGTTCTGGGAACA	9972
rs185351245	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622819	GAATCCTGATCTAAC[C/T]TTACAGTGTCTCTAT	9972
rs185358252	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657191	GGTGTGACTTTGCTG[C/T]ACTGAACAGTTTATT	9972
rs185364190	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640709	GCATCCTCAAACTCC[C/T]GGGCTTAAGCAATCC	9972
rs185427783	snp	C/T	0.00676609	0.0577691	intron-variant	NUP153	GRCh38.p7	6:17618812	ACCTCGTGATCTGCC[C/T]GCCTTGGCCTCCCAA	9972
rs185433954	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17676098	AGAAAGTAACTTCTG[C/T]CTTATAGTCCTATCA	9972
rs185435246	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653515	TATGATGGCTCCTTA[A/G]AAAGTTAAACATACA	9972
rs185468653	snp	C/G	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17649559	AGATAGTAATTCTTA[C/G]GATATACTACAGTTG	9972
rs185523926	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669944	TATTAAAATACAAAA[A/C]ATTAGCCAGGCGTGG	9972
rs185530408	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17687991	AGGTGTGGTGGCAGG[C/T]GCCTGTAGTCCCAGC	9972
rs185540234	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17702938	GGCGCGGTGGCTCAC[A/G]CCTGTAATACCAGCA	9972
rs185551776	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17660298	CATTGGTCAATGAGG[A/G]AGTCACTGGTGAAAT	9972
rs185569526	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635132	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	9972
rs185571147	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692930	TAATCTTCAGTTATC[C/T]AGAAAAAATATACAT	9972
rs185858157	snp	G/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17627669	CCCGGATTGTCTTTA[G/T]ATTTAAACACATTTG	9972
rs185898830	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694387	ATAGGAGCTGGGCCC[A/G]GTGGCTCACGCCTGT	9972
rs185904211	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17619533	AGAAAAGTTCTTTCA[C/G]TGCTTACTTCAGCAG	9972
rs185999442	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17645080	ACACAACAAGGCTCC[A/G]TCTCACAATTAAAAG	9972
rs186024373	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17650114	CTTCTACCTGATAAA[C/T]GTTTAGATATATGAT	9972
rs186027367	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677073	TGTACCAAAAGGTTC[A/G]CCCTTAAAAATAAGG	9972
rs186038915	snp	C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17641909	TAAAAGTTGAAGCTG[C/G]CTAAATAGTATATGG	9972
rs186125514	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641407	GGGTGTGGTGGTACA[A/C]ACCTGTAGTCTCAGC	9972
rs186137805	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673203	GAGAAACTCCGTCTC[C/T]ACTAAAAATACAAAA	9972
rs186150665	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17661711	CGTCTCATCTTGCCA[C/T]CTCCACCACCTACTC	9972
rs186172667	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650746	GAATATGTGAGCAAA[C/T]AAAAACTTTTTTCTC	9972
rs186181301	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17683529	CTTTTTGTCCCCAAG[C/T]AAGAGGTCTCAACAA	9972
rs186199465	snp	A/G	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17695474	AATTTTACCTAAAAG[A/G]CCACCATTTTAATTA	9972
rs186210953	snp	C/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17703170	GCCACTGCACTCCAG[C/G]CTGGGCCACAGAACG	9972
rs186234183	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17623142	CTCAAAAAAAAAAAA[A/G]AAAGACGATGACAAC	9972
rs186243510	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17616986	CGATCTCCTGACCTT[A/G]TGATCTGTCCACCTC	9972
rs186269372	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657815	TTGCAGTTTTGCATT[A/T]TAACAATTTGCCACT	9972
rs186275086	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646262	GCCCAGGCTGGAGTG[C/T]AGTGGCGCAATCCTG	9972
rs186283418	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662749	AACTGGTAGCCTGTG[C/T]CTTCTGAACAGTGAG	9972
rs186283612	snp	A/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17678138	AGGCGGGCAGATGAC[A/T]TGAGGTCAGGAGTTC	9972
rs186286898	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17662451	ATACTTCCACTGAAA[A/G]GAATCAAGACTTCTT	9972
rs186288887	snp	G/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17645322	TTTTTTGAGATAGGG[G/T]CTTGCTCTGTCAGCC	9972
rs186307348	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632499	TATTCAGAAACAGAT[A/G]TAACTAAAACATCTC	9972
rs186324533	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665701	CAAAACAGCACTACA[G/T]ATCAAACCTTTTACA	9972
rs186341977	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699733	CCAGTTACTCAGGAG[A/G]CTGAAGCAGGAGAAT	9972
rs186356307	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17628283	TATTTGTAAATAAAG[C/G]CCTTCCCATAGATTA	9972
rs186478590	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683379	GGAAAGTCAAAATGC[C/T]TCCTTGATCCATGGG	9972
rs186486670	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698941	TTACCTACAAGATAC[A/T]ATCACACTTTTTCTC	9972
rs186670809	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632214	GGCTGAGGCAGGGAA[C/T]TGCTTGAACCTGGGA	9972
rs186744813	snp	A/G	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17665986	GAGGCAACTCACCTG[A/G]CTTTTTTTTTTTTTT	9972
rs186747976	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17684450	AACTGAAGGGAGTTA[A/G]GGCTTGCTCTGGATT	9972
rs186808059	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17633168	AAAATCATGCTCGCA[A/G]ATTAGGGGCTCAAAG	9972
rs186817094	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617572	TTATCAGTGGGTGCA[A/G]TGACTCATGCGTATA	9972
rs186827733	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17651462	ATATCAAAAATTATA[A/T]TAACTATAAATGGAT	9972
rs186888223	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17616391	TCCAGAATTATAGTA[C/T]GGTAAATTTATGTTG	9972
rs186931379	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17635397	TACAGGTGTAAGCCA[C/T]CGCACCCGGCCTATC	9972
rs186949568	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17668660	CCAGTCTAGCCAAAA[C/T]GGTGAAACCCTATCT	9972
rs186972621	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702385	GGTGGCAAGGCACCT[A/G]TAGTCCCAGCTACTC	9972
rs186993414	snp	C/G	0.00874735	0.0655527	intron-variant	NUP153	GRCh38.p7	6:17677559	TTAAAATTATTTTGA[C/G]TAGGATCACACTGAA	9972
rs186995836	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625454	AGAATTGCTTGAACT[C/T]GGGAGAGGCAGGTTG	9972
rs187002202	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17618767	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	9972
rs187007059	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658201	CAGGAGTTCAAGACC[A/G]GCCTGGTCAAGATGG	9972
rs187008606	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17643129	AAGGTACTAAAGGCC[A/T]CTGAATTATTCCCTT	9972
rs187027648	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17674382	CACATATCTAATACA[A/T]AAAACACTCACTTAG	9972
rs187146353	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654344	TTTTTTTTTTGAGAC[A/G]GAGTTTCGATCTTGT	9972
rs187157080	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687230	AAAGATCATTTCTAC[A/T]GCTATCTTAGAAGAC	9972
rs187180185	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17689285	CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT	9972
rs187215117	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17695197	AATCTGTGTAATCTT[C/T]AGTTCTGTAGTTTAT	9972
rs187232349	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657984	ACAAAAGACAAGTTC[A/G]AGCGATTTTCTTATT	9972
rs187239546	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17622093	GACTTTGTAGCATGG[C/T]TTTTCTTTTGTTTTG	9972
rs187245771	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656305	TATAACTTCAGGGTG[C/G]AACAGAGCCAGTGAT	9972
rs187248379	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17638233	TGCTGTGGTATTCTC[C/T]ACCTTCAGTAAAATC	9972
rs187253347	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17671816	AGTTCGAGACCAGCC[C/T]GGCCAACATGGTAAA	9972
rs187276364	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17691491	GACTTAAGGCTGGGC[A/G]TGGTGGCTCATGCCT	9972
rs187466843	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673870	TATTTGTATTTACCT[A/G]AGATGAAAATGAATG	9972
rs187476914	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17623984	ACAGCATTTGCTTCA[A/G]TATTACACTGTTCAC	9972
rs187485978	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17680955	TAAAGGAAACTAGTA[C/T]ATCAAAGAGATAATC	9972
rs187495190	snp	A/G	0.0146672	0.084371	intron-variant	NUP153	GRCh38.p7	6:17696522	GTACTTTGAGAGGCC[A/G]AGGCGGGTGGATCAC	9972
rs187559639	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630178	AAAGATTTACAAGAA[A/G]CTAACCACAGTTACA	9972
rs187572065	snp	A/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17663780	AATAAGGTGTTAAGT[A/T]AACAAAATAAATACA	9972
rs187573366	snp	C/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17646968	CACTATGTTGGTCAG[C/G]CTGGTCTCGAACTCT	9972
rs187666676	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620352	CCACGTATTTACAGC[C/T]AACTGATTTTCGACA	9972
rs187673082	snp	A/G	0.000279452	0.0118173	intron-variant	NUP153	GRCh38.p7	6:17637784	ACCTACAATGAACGA[A/G]GGAGAGAGTGCAACG	9972
rs187680073	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643246	GAGACGCCTAGGCGG[C/T]CAGATCACCTGAGGT	9972
rs187699199	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17700338	TTTAACCTCCACAAC[A/C]ATTTTCACTTTACAG	9972
rs187706780	snp	G/T	0.00914312	0.0669923	intron-variant	NUP153	GRCh38.p7	6:17675088	CCCAGGAGGTGGAGG[G/T]TGCAGTGAGTTAAGA	9972
rs187728388	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17680052	CCATGTCAATTCCTG[C/T]GCTTTGCCTAATAAA	9972
rs187830444	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666748	TGCTAAACTGAAACA[C/T]AGTAAAAATCCTGTT	9972
rs187846905	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686025	TGGTAGCACACGCCT[A/G]TAGTCCCAACTACTT	9972
rs187852909	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700902	TGACCCCTGATCTAA[A/G]CTACTGATAAAGAGG	9972
rs187940255	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652731	CCTAAAACTCAGTAA[G/T]AAGACAGCTGGCTGG	9972
rs187952673	snp	C/G	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17686445	CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGTGCGA	9972
rs187989771	snp	C/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17659357	TGTTCAATAAAGATG[C/T]GTTTGAGCCTAGTTA	9972
rs188003488	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17692563	AAGAAGGAAGGAAAA[C/T]AATAAAATGGACCTG	9972
rs188037000	snp	C/G	3.31208e-05	0.00406931	missense	NUP153	GRCh38.p7	6:17629218	TGAAATGGAGTTAAA[C/G]AAACTGGGTTGCTTA	9972
rs188055592	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663159	AGATAGAGCAAATGT[A/G]GTAAAATGTGAAGTT	9972
rs188064377	snp	A/C	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17695648	ACAGCCAACTATAAG[A/C]CATTAGAAATTTTTA	9972
rs188110962	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17634211	TCTTCCTCTGAAGCA[A/G]CCAGTGCCATGTAGT	9972
rs188147823	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17701593	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	9972
rs188220913	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666871	ACAACATTGGTTTCC[A/C]GGGCAAAGCCTCTGT	9972
rs188245160	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701385	ATACAAAAATTAGGC[C/T]GAGTGTGGTAGCTCA	9972
rs188317293	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17646509	CCGCGCCTGGCCCAA[A/C]TATAGAGGTTATTTT	9972
rs188341017	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17679461	AGCAATCTACAGATT[C/G]AATATAACCTCTATG	9972
rs188399427	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17635013	GCAAAAGAATCTCAT[A/C]ATGTTTTAGAAAATT	9972
rs188405383	snp	A/G/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17618777	TTCACCGTGTTAGCC[A/G/T]GGATGGTCTCGATAT	9972
rs188407232	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17653256	AGGCTCCATCTCAAA[A/G]AAAGAACTGAACAGA	9972
rs188421121	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667216	TACTAATAGATTCCT[A/T]CTTGCCTAATTCCAA	9972
rs188493784	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671641	TGGGAAGATATACCA[C/T]GTTCATGGTTTGGAA	9972
rs188504100	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703924	CAACTCTAAGACACC[C/T]TGGATCATAGGTGTT	9972
rs188518723	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644882	CGAGGTTAGGAGATC[A/G]AGACCATCCGAGCTA	9972
rs188528895	snp	A/G/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17661330	AAAAAAGAAGAATAC[A/G/T]TATAGTATTAATCCT	9972
rs188529096	snp	A/G	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17676562	TTTAGAATTGTTTCT[A/G]AAGTTCCCAAAAAGA	9972
rs188543312	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693950	TCTTTACTTTTTCAG[C/G]TCTTTGCTTATATAA	9972
rs188563132	snp	G/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17657510	TGGAGGGTGCCATGA[G/T]CCAAGATCGTGCACT	9972
rs188581263	snp	C/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17620230	TATCATACTATCTGA[C/T]TTCAAAATATACTAC	9972
rs188581729	snp	A/C/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17673076	AAGATGTCATCAAAA[A/C/G]TAAAACTTCTGGCTG	9972
rs188583810	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17690366	TCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA	9972
rs188595931	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17655195	GGCCAATATATTTAA[A/T]GACTACAATCCTTGC	9972
rs188769274	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17655682	TGGTCTCGAGCTCCT[A/G]ACCTCAGGTGATCTG	9972
rs188779801	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17688837	AAGGCAATAATTGTC[C/T]CAAATGGCTGCATTA	9972
rs188847327	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633902	CACAAACTCTCATTT[A/G]CTCCAGTGGTTTTTA	9972
rs188891782	snp	G/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17671298	TGATTTTGGTCTCGG[G/T]GTAATAATGTTGGCC	9972
rs189017602	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17696082	GATGTTCCAGTTGAT[C/T]GTGCCATTGCACTCC	9972
rs189038702	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17677373	CCAATATAGTAAAAA[C/T]TCAATGTATAGAAAA	9972
rs189064607	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640421	CTGATTACACAACAA[G/T]TTACAAAACTAATCA	9972
rs189070584	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622605	TAGGGCCTCTGTAGC[C/T]TTTTCTCAATTCTTT	9972
rs189072585	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657128	TTCGGCTGAAGCTCA[A/G]GTTGATTATTTATAG	9972
rs189120455	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17652006	AGGCTCAGGTGGCCA[C/T]GCCACTGCACTCCAG	9972
rs189314542	snp	C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17645211	CCGTGCCATTGCACT[C/G]CAGCCTGGGCAACAG	9972
rs189319876	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17662187	GATGGCTTTTTAGTT[A/G]ATGAATCCTGAAATT	9972
rs189328670	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17694402	GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTCC	9972
rs189370822	snp	C/G	0.0138799	0.0821421	intron-variant	NUP153	GRCh38.p7	6:17698503	CAGCACTTTGGGAGG[C/G]CGAGGTGGGCGGATC	9972
rs189409422	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17626498	CAGCTGTACTTTTAT[A/G]TGTTTTATTTTGCAA	9972
rs189413465	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17660752	TGAAGAGAAAACATG[C/G]CAACATCTAATACAG	9972
rs189417771	snp	A/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17644215	TTTTGAGGATCTAGT[A/T]TTTAAAAATTCCCAA	9972
rs189419220	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615671	CATCCGTTTCAACAC[C/T]CTCTAATCTATACAG	9972
rs189430775	snp	C/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17631882	TGAAGCAGGAGAATG[C/G]CATGAACCCAGGAGG	9972
rs189452306	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649789	CTCTGACTGTGCCTA[C/T]TTATAAATTAAATTT	9972
rs189454624	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707620	ATGCAGTCAGCTAAC[A/G]TTAGGGGTAAGTGAT	9972
rs189460377	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17664770	ATCTGACCAAGGTAG[C/T]GGCCAGGCGCGGTGG	9972
rs189462524	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683011	ATAAGATATTGCAGT[A/G]ATTCAGTCACATCTT	9972
rs189492598	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686907	GGCGGGGGAGGGGGG[C/T]GGGGAGTGGGGGGTG	9972
rs189505263	snp	A/C	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17701865	AGCTAAATGCAGGAA[A/C]TGACTTGTAAGACAA	9972
rs189520910	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17627097	CTCAGTTCCAATACC[A/G]CACACTATCCAGGGC	9972
rs189574202	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17619959	AAAAATTAGCCAAGT[G/T]TGGTGGCACGCGCCT	9972
rs189581739	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17664291	TAACAGTTGAACAAC[C/T]CACAGACACCACTTT	9972
rs189582253	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17654779	CATTTCACAATTCAC[C/T]ATCTAATACCTTTGT	9972
rs189589251	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17636780	AAGAAACCTTCCCTG[C/T]AAATGACCACTAGCT	9972
rs189593669	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670281	AAACAGGAAAGCAAG[C/T]ACAACATCTAAAAAC	9972
rs189600257	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17627746	ACTGTTGTTTTTAGC[A/G]TGTGATGTTACAAAT	9972
rs189608537	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17688097	CACTCCAGCCTGGGC[C/T]ACAGAGCGAGACTCC	9972
rs189615577	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702985	GCGGGTGGATCACCT[G/T]AGGTCAGGAGTTTGA	9972
rs189681498	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17631178	AAATAAAACAGAAAA[C/T]ACCAGGGAACCTTAC	9972
rs189763169	snp	G/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17702447	CGGGAGGCAGAGCTT[G/T]CAGTGAGCAGAGATC	9972
rs189845203	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17672451	AATGGTGGCACACGC[C/T]TGTGGTCCCAGCTAC	9972
rs189859617	snp	C/T	0.0248432	0.108648	intron-variant	NUP153	GRCh38.p7	6:17681441	ATACAAAAAATTAGC[C/T]GGGTGTGGTGGCGGG	9972
rs189861977	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708468	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	9972
rs189937418	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17648985	AACACTCCATTATAA[C/T]GTATCCAAGATATTT	9972
rs190071359	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17619627	TTTGTGAAGTGTTCT[A/G]TATTTTTAAACTAAA	9972
rs190081612	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635645	TTCAAGCAATATACC[C/T]GCCTTGGCTTCTCCC	9972
rs190100335	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648409	ATCACCTGAAGTCAG[A/G]AGTTCAAGATCAGCC	9972
rs190103287	snp	A/G	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17690221	GCCAGGCGTGGTGGC[A/G]GGCGCATGTAGTCCC	9972
rs190123722	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17617029	TGCTGGATTACAGGC[A/G]TAAGCCACTGCACCC	9972
rs190125659	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641081	TCCTTGTATTTAGAG[A/T]TCTACATTTTCAGTG	9972
rs190138556	snp	A/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632522	AACATCTCAGGATAA[A/T]CTCATTTTATATTAA	9972
rs190166286	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17678556	AATGATTACTTGCAT[G/T]CCTTGATTAATGCTC	9972
rs190168415	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17662987	GACATGACAACTAAA[C/T]GCAAGACATGATGTT	9972
rs190182676	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695485	AAAGACCACCATTTT[A/C]ATTAGTATCTTATTG	9972
rs190230200	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622377	GGCTCAGGCAGGAGG[A/T]TGGCTTGAGCCCAGC	9972
rs190340875	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17630594	CTTGAGCCCGGGAGG[C/T]AGAAGTTGCAGTGAG	9972
rs190357215	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17656831	GTCTCTTCATGCCTC[C/T]TTATGGGCCACATGT	9972
rs190371068	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17689862	GAAAGGGAAAGTAAT[A/G]TGGTATAATAGCTTT	9972
rs190395312	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17635141	TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC	9972
rs190402676	snp	C/G/T			intron-variant	NUP153	GRCh38.p7	6:17693144	CACTTGGATTTAAAG[C/G/T]TTTTCTTTACTCACT	9972
rs190408798	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17667676	CTGCGACTGTGCCAC[C/T]GCACACTCCAGCCTG	9972
rs190505778	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642099	AAAATGGATCAATAT[C/T]CTAAATATGACATAA	9972
rs190509441	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624398	AGTCTGTGAAACCTG[C/T]GAATGTTGTTTATAT	9972
rs190517618	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658104	AGTGGTGGTTAAAGA[A/C]GTTTTGCAAAGGAGG	9972
rs190519907	snp	G/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17683396	CCTTGATCCATGGGC[G/T]GCAGAATGGACATTG	9972
rs190521913	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699074	GGCATCCTATCATCC[C/T]GTTTCTGACAGTAAA	9972
rs190527816	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673912	CATTCATAGCAGCTT[A/C]ATTCATAATTGCCAG	9972
rs190597532	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17638649	CTTTTTCTTCTACTT[C/T]TTCAGATTTTCCTAA	9972
rs190607939	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17672219	GGAAAGACACACAGA[G/T]CAATGGGTGGGTCGG	9972
rs190637075	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676121	TCCTATCATTCTGAG[A/C]CCATAAAAAATAAGT	9972
rs190641203	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653923	AACAACAAATATTTA[A/G]CTCTACTTCACGCTA	9972
rs190726859	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618937	AAAGACAAAAGGTAA[C/G]AAGGAAAGGAAGGAT	9972
rs190799309	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633244	AAGCATTCTAAGACA[C/T]AAGATGTAAATTGTA	9972
rs190807199	snp	A/G	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17651629	ACTAAGCATAAGAAG[A/G]CTTATTCCAGTAAGA	9972
rs190821453	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666108	CTGGGATTACAGGCA[C/T]GAGCCACTGCACCTG	9972
rs190827406	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17685243	CAGATATATAGTCAT[A/G]TGCCACATAAGAACA	9972
rs190837880	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17700462	ATCAACTATCCAATC[C/T]TATCAATGTTTCCAT	9972
rs190851022	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695925	GAGGCAGGAGAATGG[C/T]GTGAACCCGGAAGGC	9972
rs191056487	snp	C/T	3.31071e-05	0.00406847	synonymous-codon	NUP153	GRCh38.p7	6:17628731	CTTCTCAGATGGTTT[C/T]GTCATACTAAAACTA	9972
rs191064539	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662463	AAAGGAATCAAGACT[G/T]CTTGGAAAAATGGCT	9972
rs191068551	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645410	GCAATCCTCCCACTT[C/G]AGCATCCCAGGTAGC	9972
rs191082112	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677653	GGTTCAGATCTCCTT[C/T]ATGTCCCTCAGTGGA	9972
rs191091595	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17687787	ACACTGAGAGATAAA[C/T]TGGGCTTCATCGAAA	9972
rs191178635	snp	C/T	0.00597247	0.0543191	intron-variant	NUP153	GRCh38.p7	6:17654424	CCTTCTGGTTTCAAC[C/T]GATTCTCCTGCCTCA	9972
rs191184677	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695228	ATATCTAGTCACTTA[C/T]AAAAGGACTAAAACA	9972
rs191228818	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17665744	TTTTTTTTAAGAGAC[A/G]GACTCCTGCTCTGTC	9972
rs191234113	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17656442	AGTTTTTTTTATTTG[C/T]TATTTTTTTAAAGAC	9972
rs191234388	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17638382	TTACACACAACACCA[C/T]CATCTGTGATCTGTT	9972
rs191250838	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17672001	CAACAGAGCAAGATC[A/C]CATCTAAAAAATAAA	9972
rs191252784	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689413	ACAAAACAAATAAAC[A/C]AACAAAAAAAAACAA	9972
rs191262613	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705111	TTTAACAACATCAAC[C/T]ATGTGAAAGTGTGTA	9972
rs191324332	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17646325	CCATTCTCCTGCCTC[A/G]GCCTCCCGAGCAGCT	9972
rs191346142	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699880	AGTGACATCAGACTA[C/T]AATTTTTATTTTACT	9972
rs191425316	snp	C/T	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17623022	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	9972
rs191435536	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650197	CAAAAGCAAGAAGAA[A/G]CTGGATGGGAGAGGA	9972
rs191467526	snp	C/T	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17651081	CCAAGGCAGGACAGC[C/T]TGAGGCCAAGAGTTC	9972
rs191583568	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683714	ACAGTCACCAGTTGC[A/G]TTAACCCCTAATAAG	9972
rs191631628	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17691539	GGAGGCCGAGTCTGG[C/T]GGATCACTTGAGGCC	9972
rs191691247	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17632245	GGCGGAGATTGCAGT[A/G]AGCAGAGATCGCGCC	9972
rs191707726	snp	A/G	1.83511e-05	0.00302907	intron-variant	NUP153	GRCh38.p7	6:17637805	GAGTGCAACGTTAGA[A/G]AAGCTTTATAAATCA	9972
rs191713308	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17621661	ACAAGTTGATCTCAT[A/G]AAGGTAGAGAACAAA	9972
rs191724337	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17655906	CCTATTCTATACAGA[C/T]ATAAAACACAAGGTA	9972
rs191728942	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671663	GGTTTGGAAGACTCA[A/G]TTTTGTTAAGATGCC	9972
rs191731592	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17616438	TTACCCAAACCATAC[A/G]GAATCTTGATGACTT	9972
rs191886366	snp	A/C	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17626580	AGCCAAGTTTCTCCA[A/C]AGCATCAACTAGTAC	9972
rs191890439	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17657865	TTAAATGTGGTTACA[G/T]TATACATCATTTTAA	9972
rs191897191	snp	A/C	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17661028	AGGCAAGCAAGAAGA[A/C]GACAGGCAGGGCACG	9972
rs191899700	snp	C/T	0.0103295	0.0711199	intron-variant	NUP153	GRCh38.p7	6:17644260	TGAAGAAACGCTTTT[C/T]GATAAGGTAATATCT	9972
rs191902106	snp	A/G	0.00914312	0.0669923	intron-variant	NUP153	GRCh38.p7	6:17618768	AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	9972
rs191904416	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17691103	GCTAAGATCACGCCA[C/T]TGCACTCCAGCCTGG	9972
rs191906869	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701118	TAATTCCAGCTACTT[A/G]GGAGGCTGAAGCAGG	9972
rs191917022	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17634303	TGCCACTCCCTGTAA[A/G]TTAGCGGACTTTCAT	9972
rs191917746	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676143	AAAATAAGTTTTACC[C/T]GTATTTTGATACTGT	9972
rs191922894	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17658439	ACACCCAAAGAAGCA[C/T]ACAATAACAACAAAA	9972
rs191923206	snp	C/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17674397	TAAAACACTCACTTA[C/G]GTCTAAAATAATGTT	9972
rs191924504	snp	C/T	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17693463	CCACTCCAGTTACAG[C/T]ATTTCTTCCCTGTAT	9972
rs191929415	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17692037	TGTTTAGCTACTAAA[C/T]GTATCAGAGATTCCT	9972
rs191937052	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652816	ATCACCTAAGGTCAG[G/T]AGTTCGAGACCAGCC	9972
rs191946848	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17623660	GTAAATAAACTGCAG[C/T]ATATTCATACAATGA	9972
rs192001496	snp	A/C/G	3.29838e-05	0.00406092	missense	NUP153	GRCh38.p7	6:17637686	CCACTAGAAGAAAAG[A/C/G]TACTTATTGCTGGTC	9972
rs192095643	snp	C/T	0.00676609	0.0577691	intron-variant	NUP153	GRCh38.p7	6:17671433	GAAGCTATCTGAGCC[C/T]GAAGCTTCTTTGCTG	9972
rs192110286	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703711	AATACTTTCCTTGGG[C/T]AGTGGTAGTTTCTGC	9972
rs192138068	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17679619	GATTTTAAAACTTAA[C/T]ACAGAAGTACAGTAA	9972
rs192167115	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696559	AGGAGATCGAGACCA[C/T]CCTGGCTAACACGGT	9972
rs192203515	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673431	AGAAAATATTCGCAA[A/C]ACATATAACAAAGTA	9972
rs192205667	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17646578	TATAGTTTATAATAT[C/T]TCACTATCTCTAAAA	9972
rs192220460	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17622115	TTTGTTTTGTTTTGT[A/G]TTTTTTTGGACAGTT	9972
rs192281781	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641490	CAGTGAGCCAAGATC[A/G]TGCCACTGTACTCCA	9972
rs192325031	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620340	TCAGAAACAAATCCA[C/T]GTATTTACAGCCAAC	9972
rs192378252	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692692	CTTAATATAATTGAG[A/T]GGTCCTCAAAGTGTG	9972
rs192407887	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17617658	GAACAACCTAGGCAA[C/T]ATGGCGAGATCCTAT	9972
rs192465003	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17655415	TCTTCCAAAGGCCCA[C/T]GAAAATGCCGCCCCC	9972
rs192483203	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17688730	GTGTCCAACAAGTTT[A/G]CCAAAATTCAGTTAC	9972
rs192616594	snp	A/G	0.00109409	0.0233634	synonymous-codon	NUP153	GRCh38.p7	6:17629358	AAATTTAAAGCCTTC[A/G]CTCATGGGGTTTATA	9972
rs192630574	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663630	GAGATAAAGCAAATA[C/T]GACAAAATGTTAATG	9972
rs192651990	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630402	TGGTAGCTCACGCTT[A/G]GAATCCCAGCACTTT	9972
rs192664001	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630703	GAGAGCAGAGGAGAC[G/T]GGAGACGAGAGGGGA	9972
rs192664078	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17688964	GCATCCATTTTTTCC[C/G]AGTATGTTAAAACAT	9972
rs192674597	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647558	TAAGGGACACATGGA[A/G]AAGAATTAAGGAAAT	9972
rs192684776	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17663886	AAACCTATGATCCAG[C/T]AATTCTATTTCTAGG	9972
rs192693731	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17696136	TGTCTCAAAACAAAC[A/C]AACCAACCAACCCCA	9972
rs192742004	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676004	AGAGTGATGTGATAC[A/G]ATACAACAGTTGAAA	9972
rs192756774	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17701540	GGTGGCACGTGCCTG[G/T]AGTCCCAGCTACTCG	9972
rs192784150	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643149	ATTATTCCCTTTAAA[A/T]TGGCTGTATCATGTC	9972
rs192800669	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17666953	AACTCAATAAGAGAG[C/T]CTATTTTGTAGACTG	9972
rs192810743	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17686212	GCCTTAGGTAAGTCC[C/T]TCTGGAAGTATTCCA	9972
rs192843207	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618431	AAAAATCTGAACTCC[A/C]TATCTTTAATGAATA	9972
rs192850986	snp	C/T	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17652426	TAAATAATCCATGGG[C/T]CAAATACAAAAATCA	9972
rs192883127	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17648604	CCTGGGTGACAGGGC[A/G]AGACTCAAGCTGAAA	9972
rs192928570	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17664192	CACTATGCTAAGTGG[C/T]TACTGACGGGTATGG	9972
rs192934278	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625455	GAATTGCTTGAACTC[C/G]GGAGAGGCAGGTTGC	9972
rs193011082	snp	C/T	0.0718919	0.175435	intron-variant	NUP153	GRCh38.p7	6:17686458	TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG	9972
rs193017296	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666859	CAGCAGCTGTGAACA[A/G]CATTGGTTTCCAGGG	9972
rs193056968	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634031	TAGCTTGGCTGGATA[C/G]TCCTCCTCCTCTACA	9972
rs193068881	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17626250	TACAATTGCTAGAAT[C/T]TTCCTACCCTAGAAT	9972
rs193076846	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660250	TAAATAGGAAAAGCA[C/T]GTTTAAAAAGCTAAA	9972
rs193129737	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708019	GAGTCTTGCCCTGTC[A/G]CCCAGGCTGGAGTGC	9972
rs193151342	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17672232	GATCAATGGGTGGGT[C/T]GGGGGAGGGATGGTC	9972
rs193169320	snp	A/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704545	TAAATCTGCTCGCAA[A/T]TACCCCTTTTCTTCA	9972
rs193171019	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17681046	AAATGAATGGACAAA[A/G]AAACTGTGCTACATA	9972
rs193236189	snp	C/G	0.0103295	0.0711199	intron-variant	NUP153	GRCh38.p7	6:17643488	CCCAACCATCCCCAC[C/G]AAAAATAACCACCAC	9972
rs193281232	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689983	TATGAACTAATATCC[C/T]CACCTTATGGATAAG	9972
rs199498669	snp	A/C/G			intron-variant	NUP153	GRCh38.p7	6:17655425	GCCCATGAAAATGCC[A/C/G]CCCCCACAAAAATAA	9972
rs199503991	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686429	TTGAGACGGAGTCTC[A/G]CTGTCGCCCAGGCTG	9972
rs199524934	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17648636	AATAAATAAATATTT[-/A]AAAAAAAATTTTTTT	9972
rs199577613	snp	C/T	0.000411804	0.0143434	missense	NUP153	GRCh38.p7	6:17661691	CAACAAAGCGTGTTC[C/T]TTCTCGTCTCATCTT	9972
rs199633776	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648075	AACTGTGTTATAAAA[C/T]GTGGCTTCCTCTAAG	9972
rs199683224	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677731	CATAATTTTTTTTTT[C/T]CTTTTTTTTTTTTTT	9972
rs199696824	in-del	-/ACAC			intron-variant	NUP153	GRCh38.p7	6:17693184	ATTTAGCTTTTTCCT[-/ACAC]ACACACACACACACA	9972
rs199710735	snp	A/G	0.00133477	0.0257993	synonymous-codon	NUP153	GRCh38.p7	6:17625842	TGTGGCTCCAAAGCC[A/G]AAACCAGAGGTGGTA	9972
rs199723958	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656680	CTTAGATAACCAACA[A/T]GGAAGACAGGAGTCC	9972
rs199739841	snp	C/G	0.000399281	0.0141238	missense	NUP153	GRCh38.p7	6:17616560	GGAGACTGGTTAAAT[C/G]GAAAGCCCCCCGAGC	9972
rs199769517	snp	A/C/T	8.24116e-05	0.00641871	missense	NUP153	GRCh38.p7	6:17669495	TTGAACTGGTCACAC[A/C/T]GTAAGATTGTGCACT	9972
rs199811963	in-del	-/ATATT			intron-variant	NUP153	GRCh38.p7	6:17657777	TGGTATATGAATCAG[-/ATATT]AGGTTGGTGCAAACG	9972
rs199857527	in-del	-/ATC			intron-variant	NUP153	GRCh38.p7	6:17635102	TGCACAGCTTGGCTT[-/ATC]TTTTTTTTTTTTTTT	9972
rs199861173	in-del	-/TA			intron-variant	NUP153	GRCh38.p7	6:17666003	TTTTTTTTTTTTTTT[-/TA]AATGGAGACTAGGTC	9972
rs199878758	snp	G/T	0.000197736	0.00994127	missense	NUP153	GRCh38.p7	6:17674985	TTCCAGGATAAAAAG[G/T]AGAATCTCCAAGCTG	9972
rs199891939	in-del	-/A	0.250732	0.249999	intron-variant	NUP153	GRCh38.p7	6:17636335	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9972
rs199900008	snp	C/T	9.89821e-05	0.00703429	synonymous-codon	NUP153	GRCh38.p7	6:17629400	GGATGACACACCTAT[C/T]TTGAATCCTCCCTGA	9972
rs199930339	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689987	AACTAATATCCCCAC[C/T]TTATGGATAAGACAA	9972
rs199994282	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701843	GTCTCGGGGGGGGGG[A/G]GAAAAAAGCTAAATG	9972
rs200023461	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17679786	AGTCACAAAAAGAAA[G/T]CAGCCATTCTTCGGT	9972
rs200024702	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693183	AATTTAGCTTTTTCC[C/T]ACACACACACACACA	9972
rs200059221	snp	A/G	1.65045e-05	0.00287263	missense	NUP153	GRCh38.p7	6:17616572	AATGGAAAGCCCCCC[A/G]AGCCTGAAGGCTGGG	9972
rs200071552	snp	C/T	3.29783e-05	0.00406055	synonymous-codon	NUP153	GRCh38.p7	6:17649277	CGGTAGAGAGATTTT[C/T]GGTAATACTGGAACT	9972
rs200077609	in-del	-/GAGGGGA	0.0399052	0.1355	intron-variant	NUP153	GRCh38.p7	6:17630753	GGGGAGGGGAGAAGG[-/GAGGGGA]GAGGGGAGAGGGGAG	9972
rs200078255	in-del	-/GC/T			intron-variant	NUP153	GRCh38.p7	6:17701834	AAGACTCTGTCTCGG[-/GC/T]GGGGGGGGGGAAAAA	9972
rs200097116	snp	C/T	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17688489	GATGGTCCTCTTTAT[C/T]TTCTGGCCAGCGTGG	9972
rs200112771	in-del	-/C	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17616284	AGGGGGGTCGGGTGG[-/C]GGGGGGAGTAGACTC	9972
rs200121438	in-del	-/C/TT	0.293294	0.246223	intron-variant	NUP153	GRCh38.p7	6:17618563	AGTTAAAATCTCTCT[-/C/TT]TTTTTTTTTTTTTTT	9972
rs200132365	snp	C/G	0.000164726	0.0090739	missense	NUP153	GRCh38.p7	6:17624624	GTCCAAACACAGGGG[C/G]CTGGCTACTGCTTGA	9972
rs200137545	snp	C/T	1.64803e-05	0.00287052	missense	NUP153	GRCh38.p7	6:17675620	TTTACAAGGGAAAAT[C/T]CCGAACTGCCAATTG	9972
rs200150904	snp	G/T	1.64969e-05	0.00287196	missense	NUP153	GRCh38.p7	6:17688607	AGATTCTGTAACCCT[G/T]CTAAGAATGCCCTGT	9972
rs200171293	snp	A/C	0.000217448	0.0104248	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706316	GTAAGGCTTAATTGG[A/C]CCCTGGTGGCAACGC	9972
rs200208320	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17681519	GAACCCAGATGGAGG[C/T]TGCAGTGAGCTGAGA	9972
rs200214030	snp	A/C	0	0	intron-variant	NUP153	GRCh38.p7	6:17624862	GAAACACTTAAGTCA[A/C]CATGGTGGCTAATGT	9972
rs200238904	snp	C/T	1.73712e-05	0.00294708	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706256	CACCCGCCAGGCCAC[C/T]GCGGCGTCGGGGTCC	9972
rs200243787	snp	C/T	3.29473e-05	0.00405864	missense	NUP153	GRCh38.p7	6:17624618	GTTGCTGTCCAAACA[C/T]AGGGGGCTGGCTACT	9972
rs200247628	in-del	-/GAGG			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705595	GGTGTTGGGGGGGGG[-/GAGG]GGAGTCGCGCAGCAG	9972
rs200249361	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658580	AATCATCAAAGCTGA[C/T]CCTTTTAAACTACAC	9972
rs200260878	snp	A/G	0.000942593	0.0216889	intron-variant	NUP153	GRCh38.p7	6:17661635	AAACCTCAAGAGTAT[A/G]TGAGTATACAACCCT	9972
rs200309216	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17641851	GCGAGACTGTCTCAG[-/A]AAAAAAAGAAGAAAG	9972
rs200355512	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17645238	ACAGAGCGAGACTCT[G/T]TCTCAAAAAAAAAAA	9972
rs200363295	snp	A/G			missense	NUP153	GRCh38.p7	6:17637176	TCAGACATACAGGAC[A/G]CACACTTATTGTCTT	9972
rs200367874	in-del	-/G	0.00795532	0.062565	intron-variant	NUP153	GRCh38.p7	6:17645624	GATGCTGATTTCTTC[-/G]GTTCAGAAATTATGT	9972
rs200406494	snp	A/T	0.000197759	0.00994184	missense	NUP153	GRCh38.p7	6:17669461	ATCTTCTCTAAAGAC[A/T]GCAATATTCGCCGAG	9972
rs200418326	in-del	-/C	0.0267878	0.112589	intron-variant	NUP153	GRCh38.p7	6:17678827	GCACACAGCTGTAGT[-/C]CCAGCTACTCAAGGA	9972
rs200423236	in-del	-/G	0.0256215	0.110247	intron-variant	NUP153	GRCh38.p7	6:17618469	ACTGGAGAGTTGGGT[-/G]GGGGGGGAACCCAGA	9972
rs200425791	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17689416	AAACAAATAAACAAA[-/C]AAAAAAAAACAATCC	9972
rs200447655	in-del	-/A/AAAA	0.00148478	0.0272064	intron-variant	NUP153	GRCh38.p7	6:17703656	TAAAAAAAAAAAAAA[-/A/AAAA]GGAGAGTATTCTTTT	9972
rs200479559	in-del	-/AAG			intron-variant	NUP153	GRCh38.p7	6:17652547	TTTTCTTAGGACACA[-/AAG]AAGAATAAAAATATT	9972
rs200481376	snp	C/T	0.000201864	0.0100445	intron-variant	NUP153	GRCh38.p7	6:17616218	TAATGTGACATGATG[C/T]TCTGAGCAAAATTTC	9972
rs200482058	snp	C/T	0.00199792	0.0315431	synonymous-codon	NUP153	GRCh38.p7	6:17688484	TACCAGATGGTCCTC[C/T]TTATTTTCTGGCCAG	9972
rs200498113	in-del	-/AC			intron-variant	NUP153	GRCh38.p7	6:17682935	AGAAGAAAAAAAAAA[-/AC]AAAAAAACACTTTCT	9972
rs200504898	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17686481	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT	9972
rs200517318	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17673354	AGACCTGTCTCAGAG[-/A]AAAAAAAAAATAACA	9972
rs200522947	snp	A/C/G	4.94387e-05	0.00497165	synonymous-codon, missense	NUP153	GRCh38.p7	6:17662053	TTGTCCGGGTGTCAT[A/C/G]TTTTTTTCATATCCA	9972
rs200536140	snp	C/T	3.295e-05	0.00405881	missense	NUP153	GRCh38.p7	6:17629032	GCCACTGAAGCACTC[C/T]TGGTTTCTATGGTTC	9972
rs200556162	in-del	-/TTTC			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704770	TTTACTTTTTTTTTT[-/TTTC]TTCGAGACAAGAGTC	9972
rs200562896	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17689553	CTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCAC	9972
rs200566929	in-del	-/TA			intron-variant	NUP153	GRCh38.p7	6:17660595	ATACATATAAGAAAT[-/TA]TATATATATCCCTAC	9972
rs200578642	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17657561	GTGAGACCCTGTCTC[-/A]AAAAAAAACAAAACA	9972
rs200597764	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648478	AAAAATTAGCCGGGC[A/G]TGGTGGTGCGCACCT	9972
rs200599601	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17681074	ATATACACAATGGAG[C/T]ATTATTCAGCCATTA	9972
rs200635527	snp	C/G	0.000399281	0.0141238	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17668987	TACCTTTTCTCTTTT[C/G]GCCTGAAAATCTGTG	9972
rs200663994	snp	C/T	0.000399281	0.0141238	synonymous-codon	NUP153	GRCh38.p7	6:17675238	ACTCACAGGGGAAAG[C/T]GTTCCAAAGGCAGAC	9972
rs200684590	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17634454	ACATTTTTTTTTTTT[G/T]GAGACAGAGTCTCAC	9972
rs200690003	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691024	GTGTGCATCTGTAAT[C/G]CCAGCTACTCAGGAG	9972
rs200750922	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17656113	AGGAGGCTGAGGCAG[A/C]AGAATTGCTTGAACT	9972
rs200771105	in-del	-/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705586	GGGGGTGGCGGTGTT[-/G]GGGGGGGGGAGGGGA	9972
rs200904636	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17701840	CTGTCTCGGGGGGGG[-/A]GGGGAAAAAAGCTAA	9972
rs200912774	in-del	-/CAAAA			intron-variant	NUP153	GRCh38.p7	6:17621014	CAAAGAACTCAACAG[-/CAAAA]CAAAAACAACCAAAT	9972
rs200915978	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	NUP153	GRCh38.p7	6:17624715	TGATATAGATCCAAA[A/G]CCTGGGGGATTGGGC	9972
rs200954747	snp	A/T	1.6495e-05	0.0028718	missense	NUP153	GRCh38.p7	6:17661760	CTGCAGGCAAACTGA[A/T]ATTTGGATATGAAAA	9972
rs200972673	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631827	AAAAAATTAGCTAGG[C/T]GTGGTGGCAGGTTCC	9972
rs200972752	snp	C/T	8.23649e-05	0.00641683	missense	NUP153	GRCh38.p7	6:17637245	GATCCAATGGGCCTT[C/T]TGAATTTATCTCCAA	9972
rs200991815	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17635104	CACAGCTTGGCTTAT[-/C]TTTTTTTTTTTTTTT	9972
rs200992105	snp	A/C	0.000109957	0.00741392	intron-variant	NUP153	GRCh38.p7	6:17632860	CTAAAAAAAAAAAAA[A/C]AAACGGGGAGTGGGG	9972
rs200993034	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625524	GACAGAGCAAGACTC[C/T]GTCTCGAAAGAAAAC	9972
rs200997130	snp	C/T	0.00199792	0.0315431	intron-variant	NUP153	GRCh38.p7	6:17668958	GTTTAAATAACTAAA[C/T]GCTAAAGAAGTTTTA	9972
rs201003671	in-del	-/T	0.0138937	0.0821817	intron-variant	NUP153	GRCh38.p7	6:17686719	TATAGAAAAAAAAAA[-/T]TTTTTTAAGTTTTTG	9972
rs201017708	snp	A/G	3.29549e-05	0.00405911	synonymous-codon	NUP153	GRCh38.p7	6:17629088	AGAGGTCACTATGGT[A/G]TTAGCAGGAGCAGGG	9972
rs201025745	in-del	-/AAAAAAAAAA			intron-variant	NUP153	GRCh38.p7	6:17620096	GAGCAAGACACCATC[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	9972
rs201058306	snp	G/T	0.145366	0.22705	synonymous-codon	NUP153	GRCh38.p7	6:17626103	AGCAGAAGTGGCTGG[G/T]GTACTTGAACTAGAG	9972
rs201061884	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17665069	AAAAAAAAAAAATTT[C/T]ATCAAGGTGACAGCT	9972
rs201122253	in-del	-/A	0.0345421	0.126799	intron-variant	NUP153	GRCh38.p7	6:17669032	CCTATCAAGAGGCTG[-/A]AAAAAAAAAAAAACA	9972
rs201167154	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616713	GCAATAGTTAAAGCA[G/T]AAATACTTCATTAGG	9972
rs201187350	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17652252	ACAGAATATATTTTC[C/T]TTAAGAATTATCAAG	9972
rs201190740	in-del	-/AA	0.11963	0.213316	intron-variant	NUP153	GRCh38.p7	6:17697071	GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAATTAA	9972
rs201231288	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17655424	GGCCCATGAAAATGC[C/G]GCCCCCACAAAAATA	9972
rs201234487	in-del	-/AA			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704731	AGAAAACTAGAAGAC[-/AA]AAAAAAAAAAATTCC	9972
rs201242237	in-del	-/TTTT			intron-variant	NUP153	GRCh38.p7	6:17652247	CAACTACAGAATATA[-/TTTT]CTTTAAGAATTATCA	9972
rs201275623	snp	C/T	0.000181277	0.00951871	missense	NUP153	GRCh38.p7	6:17625979	AGGTGCTGGATTCAG[C/T]AGTGTTACCAAAGGC	9972
rs201282375	snp	C/G	8.23744e-05	0.0064172	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632708	CAAACATTTGGTAGA[C/G]TCTGCCTTATTCTGC	9972
rs201310017	in-del	-/GA	0.0193772	0.0965046	intron-variant	NUP153	GRCh38.p7	6:17616285	GGGGGGTCGGGTGGG[-/GA]GGGGGAGTAGACTCA	9972
rs201354053	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17701832	AGCAAGACTCTGTCT[-/C]GGGGGGGGGGGGAAA	9972
rs201355883	in-del	-/GGGCAGATCACTTGAA	0.0715223	0.175059	intron-variant	NUP153	GRCh38.p7	6:17693657	TTGGGAGGCCGAGGC[-/GGGCAGATCACTTGAA]GGGCAGATCACTTGA	9972
rs201358927	snp	C/T	3.29544e-05	0.00405908	missense	NUP153	GRCh38.p7	6:17688582	GCCACCCTGGCACAA[C/T]ATTCTTAACAGATTC	9972
rs201367642	in-del	-/AAAT	0.039522	0.134904	intron-variant	NUP153	GRCh38.p7	6:17648620	AGACTCAAGCTGAAA[-/AAAT]AAATAAATATTTAAA	9972
rs201371877	in-del	-/C	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17634106	ATTCTGGTTCATGAA[-/C]CCCCCCCCATTACTC	9972
rs201397162	in-del	-/GA	0.0337553	0.125452	intron-variant	NUP153	GRCh38.p7	6:17683100	CTCCACTGAAGTCCT[-/GA]ACCCCTCAAAGTTAT	9972
rs201406748	snp	C/T	0.000379003	0.0137607	missense	NUP153	GRCh38.p7	6:17662024	TGACAGTACCTTTCT[C/T]GTTGTTCTCTATTTT	9972
rs201437628	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645248	ACTCTGTCTCAAAAA[A/G]AAAAAAAAAAAAGAA	9972
rs201440195	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17654325	CTGACCTTGAACCAA[-/T]TTTTTTTTTTTTTGA	9972
rs201476251	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17628341	ATCCTTATTTTCCAG[A/G]TAGTAGATACCAATT	9972
rs201490301	snp	C/T	0.00355894	0.0420334	intron-variant	NUP153	GRCh38.p7	6:17647781	TGAAATCAGTAAATA[C/T]ATACTATTCCTTGCT	9972
rs201508746	snp	C/T	0.000164834	0.00907689	synonymous-codon	NUP153	GRCh38.p7	6:17649184	TGTTAATGCTTGAGA[C/T]GAATTGATGGGTGAT	9972
rs201512278	snp	A/G	0.00199804	0.031544	intron-variant	NUP153	GRCh38.p7	6:17637817	AGAGAAGCTTTATAA[A/G]TCAAAGCATTAATTT	9972
rs201517991	snp	A/G	0.00014844	0.00861383	synonymous-codon	NUP153	GRCh38.p7	6:17629142	AAAGCTAAAACCTGC[A/G]GAGGAAGATTTGGGC	9972
rs201525820	in-del	-/GC			downstream-variant-500B	NUP153	GRCh38.p7	6:17614637	GGGCGGGAGAACTGG[-/GC]GGGGGGGGGGGAGTG	9972
rs201638800	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17669578	ATATTATTTGTTGCA[A/G]CATAAAATCTAAGGC	9972
rs201651917	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17644051	CTGTGTTAGCCAATT[-/A]AAAAAAAAAAGATAA	9972
rs201652446	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17693778	GTAATCCCAGCTACT[A/C]GGAAGGCTGAGGCAG	9972
rs201668180	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17676861	CCCAGAAATCCACAA[-/G]GGAGTGTCCAGTGAG	9972
rs201676381	snp	A/C	0.000230947	0.0107434	missense	NUP153	GRCh38.p7	6:17629393	CAGAATCGGATGACA[A/C]ACCTATTTTGAATCC	9972
rs201712753	in-del	-/TCTTTT			intron-variant	NUP153	GRCh38.p7	6:17618561	GGAAGTTAAAATCTC[-/TCTTTT]TTTTTTTTTTTTTTT	9972
rs201725296	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17645221	GCACTCCAGCCTGGG[A/C]AACAGAGCGAGACTC	9972
rs201774934	snp	C/G/T	0.00136866	0.0261242	intron-variant	NUP153	GRCh38.p7	6:17637148	CCATAAAGCCAAAAA[C/G/T]ATACCTGGTTTCTCA	9972
rs201792750	snp	C/T			missense	NUP153	GRCh38.p7	6:17624703	TGCTGTGGAAGATGA[C/T]ATAGATCCAAAGCCT	9972
rs201840744	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695498	TTAATTAGTATCTTA[C/T]TGTCTACCAAACACA	9972
rs201843051	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17681223	CTTTAAAAAAAAAAA[A/C]CGGACTCAAAAGAAC	9972
rs201847917	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668375	GTAAGCCACCGCACC[C/T]GGCCGATCACTCCTA	9972
rs201853569	snp	A/C	0.000429553	0.014649	missense	NUP153	GRCh38.p7	6:17616567	GGTTAAATGGAAAGC[A/C]CCCCGAGCCTGAAGG	9972
rs201925739	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704234	GAGGCGGAGCTTGCA[A/G]TGAGCCAAGATCGCG	9972
rs201954304	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615272	CCCAATTTTTTTTTT[A/T]AAGATTTCCAAATGG	9972
rs201974266	snp	C/G	1.65809e-05	0.00287926	missense	NUP153	GRCh38.p7	6:17637725	ACTACTGGGCTTGTT[C/G]CGGTGGGCTGAGCAG	9972
rs202022678	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657541	CCAGCCTGGGCAACA[A/G]ATAGAGTGAGACCCT	9972
rs202054964	snp	A/C/G	3.29588e-05	0.00405938	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632694	GCACTTTCACATGCC[A/C/G]AACATTTGGTAGAGT	9972
rs202069811	snp	C/G	8.23676e-05	0.00641693	missense	NUP153	GRCh38.p7	6:17688507	CTGGCCAGCGTGGAA[C/G]CTCGCTTGTGTCTGT	9972
rs202074605	snp	C/G	3.29527e-05	0.00405898	missense	NUP153	GRCh38.p7	6:17688572	TATCTTTGTAGCCAC[C/G]CTGGCACAATATTCT	9972
rs202149653	in-del	-/TC	0.0718919	0.175435	intron-variant	NUP153	GRCh38.p7	6:17685239	ACAGCAGATATATAG[-/TC]ATGTGCCACATAAGA	9972
rs202171648	in-del	-/TGTG			intron-variant	NUP153	GRCh38.p7	6:17685242	GCAGATATATAGTCA[-/TGTG]CCACATAAGAACAGT	9972
rs202196359	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17633125	CTCCCCCTTAACCAC[A/G]TGTTTGAACTGCTGT	9972
rs202198994	snp	A/G	0.000182181	0.0095424	intron-variant	NUP153	GRCh38.p7	6:17669355	GTTAAAGTTGAAAAA[A/G]TAACAAAATTAAGAT	9972
rs202228382	snp	C/T	1.64773e-05	0.00287026	synonymous-codon	NUP153	GRCh38.p7	6:17616631	ACCAAATGTGAACAC[C/T]CCTGATGGACTGTTG	9972
rs202245961	in-del	-/A	0.0391387	0.134304	intron-variant	NUP153	GRCh38.p7	6:17644646	GAAAACCACCATTAT[-/A]AAAAAAACAAATTCG	9972
rs207466749	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628217	TCTCAGGATTAATTA[C/T]ATTTGTTGTCTATGT	9972
rs367573561	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692220	AAATACATGAACTTA[A/G]ATTACAGACCGATTT	9972
rs367620769	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17664690	CAGATAAAGCAAATC[C/T]GGCAAAATTATGTAA	9972
rs367667783	snp	A/G	1.68134e-05	0.00289938	intron-variant	NUP153	GRCh38.p7	6:17669596	TAAAATCTAAGGCAC[A/G]TATTTCATGCAGTGA	9972
rs367678082	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17703140	GAGGCAAAGGTTGCA[G/T]TGAGCCAAGATCGAG	9972
rs367683424	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683155	CTCTAAACTCCTATT[A/C]ATGTCAATATTTGGA	9972
rs367711734	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17622876	TGGCTCACACCTGTA[A/C]TCCCAGCACTGTGGG	9972
rs367727024	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667441	AAATCCAAGCCAGGC[A/G]CGGTGGCTCACGCCT	9972
rs367735885	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17648112	ACACAATCTTAGAGG[C/T]GGATATTTGTATAAA	9972
rs367780735	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653110	TATAAAAAATTAGCC[A/G]GGCATGGCAGTGTCC	9972
rs367827387	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17641789	CCTGAGAGGTGGAGC[C/T]TGCAGTGAAACGAGC	9972
rs367835835	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699498	AAAAAAAAAAAAAAA[A/G]AAAATACAAGATAAT	9972
rs367846665	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705583	GGCGGGGGTGGCGGT[A/G]TTGGGGGGGGGGAGG	9972
rs367859091	snp	A/C/T	0.000132154	0.00812778	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632817	GAGACAGGTACAGTG[A/C/T]TGCTACTTGAAGCAG	9972
rs368057538	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705084	TTTAAAAATCTGTTG[A/G]TAATGACACAATTTA	9972
rs368093538	snp	G/T	0.00120692	0.0245357	intron-variant	NUP153	GRCh38.p7	6:17616214	TTCATAATGTGACAT[G/T]ATGCTCTGAGCAAAA	9972
rs368095623	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17652750	ACAGCTGGCTGGGTG[C/T]GGTGGCTCATGGCCT	9972
rs368100666	snp	A/G	5.28667e-05	0.00514107	intron-variant	NUP153	GRCh38.p7	6:17665205	CTTATTCTAATCAAT[A/G]TTCAAAGACTGGTAG	9972
rs368106778	snp	A/C	1.7783e-05	0.00298181	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706239	CTCCAGCCGAGTTTC[A/C]CCACCCGCCAGGCCA	9972
rs368142844	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17646751	TTTCCTTTTTTTTTT[-/T]GTTTTGAGGTGGAGT	9972
rs368173527	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17680566	AACACTAAAAGCACA[C/G]GCCATGGAAGCAAAA	9972
rs368189810	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17643207	GCTGGACGCGGTGGC[G/T]CACACCTGTAATCCC	9972
rs368258849	snp	C/T	6.59109e-05	0.0057403	missense	NUP153	GRCh38.p7	6:17628940	GAGAGGCAGGCTCCA[C/T]GTTGCCAAAAGAGAA	9972
rs368278652	in-del	-/AAG			cds-indel	NUP153	GRCh38.p7	6:17665286	TCCTGAATTCACCAG[-/AAG]GAGTCAGAGATGGTT	9972
rs368285722	snp	C/G			missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706330	GCCCCTGGTGGCAAC[C/G]CCGCGTCCGGATCTT	9972
rs368351288	snp	A/G	0.000153988	0.00877328	intron-variant	NUP153	GRCh38.p7	6:17625762	CTGACACACTAATAA[A/G]TAAAGTCCATCCAAT	9972
rs368362120	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17661380	TATGTTTTACAAACA[C/G]ACAAAACTATACAGT	9972
rs368373485	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17672621	AAGCTATTCAATGAA[A/C]AAAGAACAGTCTTTT	9972
rs368386002	in-del	-/GTTT			intron-variant	NUP153	GRCh38.p7	6:17616761	TTTGTTTGTTTGTTT[-/GTTT]TTTGAGACGGAGTCT	9972
rs368386844	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676964	AGAGATACTAGACAG[C/T]GTACCGTGCTAGGGG	9972
rs368424345	snp	C/T	1.65132e-05	0.00287339	synonymous-codon, intron-variant, splice-acceptor-variant	NUP153	GRCh38.p7	6:17640048	ATTTGTACTGTTCAC[C/T]GTAGTGACATGATGA	9972
rs368448871	snp	A/G	3.29924e-05	0.00406142	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616063	AGCAGGGCACCAGCT[A/G]TTGTTAAAATTGAGT	9972
rs368518299	snp	C/T	6.7563e-05	0.00581179	intron-variant	NUP153	GRCh38.p7	6:17665230	TGGTAGAAATATACA[C/T]ATACTCACACTGCAC	9972
rs368523707	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17689425	ACAAACAAAAAAAAA[-/A]CAATCCAACAAAAAT	9972
rs368535206	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627096	TCTCAGTTCCAATAC[C/T]GCACACTATCCAGGG	9972
rs368556628	in-del	-/TTTT	0.112983	0.209108	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704760	TCCTCAAATCTTTAC[-/TTTT]TTTTTTTTTCTTCGA	9972
rs368557255	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669563	TGTAAAGTAAACCCT[A/C]TATTATTTGTTGCAA	9972
rs368579036	snp	A/G/T	4.95372e-05	0.00497656	missense	NUP153	GRCh38.p7	6:17674915	CCTACCTGATAAGGT[A/G/T]TATTTCGTAGTTTAG	9972
rs368609111	snp	C/T	4.94222e-05	0.00497078	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632755	AGTCCCAGCTTCCCT[C/T]GGGTTTCTTGAACTT	9972
rs368618308	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705372	CATTTACAATTAGGA[C/T]AATCCTTTTTTATAA	9972
rs368666025	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17630709	AGAGGAGACGGGAGA[C/T]GAGAGGGGAGGGGAG	9972
rs368723952	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667828	CAAACTATCAAACAT[C/T]GTATTTTTTTCCCAC	9972
rs368724342	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657199	TTTGCTGTACTGAAC[A/G]GTTTATTAATATTAA	9972
rs368726750	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17636105	TTGGAAGGCCAAGGC[A/G]GATAGATCACTTGAT	9972
rs368861582	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640228	ACAGGGATAATTTGC[A/C]ATTACAAGGAGATAA	9972
rs368880086	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17675971	ATTTAAATAAGAGCT[A/G]ATTTTTTTAAACCAG	9972
rs368887128	snp	C/T	1.6473e-05	0.00286988	missense	NUP153	GRCh38.p7	6:17637309	AAGATGAAGCAGTCA[C/T]AGTCTCAGCACTTTC	9972
rs368903679	snp	C/G	1.65002e-05	0.00287225	synonymous-codon	NUP153	GRCh38.p7	6:17675232	GTTAGTACTCACAGG[C/G]GAAAGTGTTCCAAAG	9972
rs368903984	snp	A/C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17686294	CCTGAAGAGTATCCA[A/C/G]TGCGACAAGATGTGG	9972
rs368905439	in-del	-/CTGA			intron-variant	NUP153	GRCh38.p7	6:17649776	TGTTGTTGTTAATCT[-/CTGA]CTGTGCCTACTTATA	9972
rs368923357	snp	A/G	6.67145e-05	0.00577519	intron-variant	NUP153	GRCh38.p7	6:17661804	AAAAAGAAAATTAAA[A/G]CAACTGATATATTAT	9972
rs368938508	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17617466	ATGTAGTGGGAATTA[-/A]AAAAAAAAAAAAAAA	9972
rs368998965	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619864	GCAGTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC	9972
rs369018001	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682265	TTGCTAACAAATAAC[A/T]ATCTGCTGAGCCTTT	9972
rs369068049	snp	G/T	1.64933e-05	0.00287165	synonymous-codon	NUP153	GRCh38.p7	6:17629139	ACCAAAGCTAAAACC[G/T]GCAGAGGAAGATTTG	9972
rs369094367	in-del	-/AAAG			intron-variant	NUP153	GRCh38.p7	6:17630670	CACTTCAAAATAAAT[-/AAAG]AAAAGAAAACAGAGG	9972
rs369107562	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17674046	AATGGATCTCAAATG[C/T]ATTATGCTAAGTAGA	9972
rs369107842	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656444	TTTTTTTTATTTGTT[A/G]TTTTTTTAAAGACAG	9972
rs369123030	snp	C/T			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707067	CGGAACGCGGCTTCT[C/T]GGAAAGGAAGAGGGA	9972
rs369129982	snp	C/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706621	GGCCGAGGAGGCTCC[C/G]GTCCGGCCGCCTCTG	9972
rs369142396	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17620797	AAAGATAGGACCCCC[C/T]TGGCCTAGGCAAAGA	9972
rs369143508	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671941	TGAACCTGGGAGGTG[A/G]AGGTTGCAGTGAACC	9972
rs369145316	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17654390	GCAGTGGTGCGATCT[G/T]GGCTCACTGCAACCT	9972
rs369223299	snp	C/T	6.75003e-05	0.0058091	intron-variant	NUP153	GRCh38.p7	6:17649139	AGAACAAATGTCACC[C/T]GTATTTATATAATGG	9972
rs369260286	snp	A/G	1.64735e-05	0.00286993	missense	NUP153	GRCh38.p7	6:17624620	TGCTGTCCAAACACA[A/G]GGGGCTGGCTACTGC	9972
rs369273457	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698340	GCTCACGCCTGTAAT[C/T]TCAGTGCTTTGGAGG	9972
rs369287938	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17635737	CTTCCTAATCTATCT[A/T]CCGGTCTCCAAATTT	9972
rs369316996	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17645937	TAAATAATAGTGCCT[A/G]CTTGCTTTTCAGAGC	9972
rs369334821	snp	C/G	6.59033e-05	0.00573997	missense	NUP153	GRCh38.p7	6:17629067	GTTGAAGCTGCTCTT[C/G]TTCTCAGAGGTCACT	9972
rs369365161	snp	A/G	1.66441e-05	0.00288474	intron-variant	NUP153	GRCh38.p7	6:17675814	TATACAACTTAGAGC[A/G]ATACACTACCACAAA	9972
rs369385782	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682734	CCATCCTTGCCAACA[C/T]GGTGAAACCCCATCT	9972
rs369446961	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698695	GTGAGCCGAGATCGC[A/G]CCACTACACTCCAGC	9972
rs369452802	snp	A/G	3.31411e-05	0.00407056	intron-variant	NUP153	GRCh38.p7	6:17661628	TTTAAATAAACCTCA[A/G]GAGTATATGAGTATA	9972
rs369461823	in-del	-/T	0.000809389	0.0201007	intron-variant	NUP153	GRCh38.p7	6:17628622	TTGTAAAAAAAAAAA[-/T]AATAATAATAATAAT	9972
rs369550223	snp	A/C/G/T	0.000494132	0.0157108	synonymous-codon, missense	NUP153	GRCh38.p7	6:17647846	CTCAGTAGATTTTAC[A/C/G/T]ATTGGAGATGAAAAT	9972
rs369583519	in-del	-/GGA			intron-variant	NUP153	GRCh38.p7	6:17672754	GAGGCTGAGGCAGGA[-/GGA]TTGCTTGAGCCCAGC	9972
rs369614968	in-del	-/TTTTT	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17647671	TGATTGTTCAAAAGT[-/TTTTT]ACACAGAGTATTTTT	9972
rs369623420	snp	C/T	0.000153988	0.00877327	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706409	GCCTCCGCCGCTTCC[C/T]GCTCCGGGGCGGGTA	9972
rs369646480	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617048	GCCACTGCACCCGGC[C/T]GCAACATGATAGGTT	9972
rs369669444	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17619251	TATATTCAATCAAAA[C/T]CTTACCAAACATGGG	9972
rs369684598	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17650227	CACTTGGAAAATGGG[-/G]AAGGGCACTGAGTAA	9972
rs369696629	snp	C/T	8.4139e-05	0.00648555	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706338	TGGCAACGCCGCGTC[C/T]GGATCTTGCCGCCAC	9972
rs369699661	snp	C/T	3.36638e-05	0.00410253	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706274	GGCGTCGGGGTCCCA[C/T]ACCTGATGCTGTTGT	9972
rs369703642	snp	A/C	0.000125256	0.00791279	intron-variant	NUP153	GRCh38.p7	6:17646184	AATATCCTTATACTT[A/C]GTTTTCAATAAGTAT	9972
rs369713141	snp	A/C			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632328	AAACAAACAAAAAAA[A/C]AAACAAACAAAAAAA	9972
rs369720380	snp	A/C/T	0.000116558	0.00763325	intron-variant	NUP153	GRCh38.p7	6:17616720	TTAAAGCAGAAATAC[A/C/T]TCATTAGGGCAAAAT	9972
rs369735765	snp	A/G	1.66893e-05	0.00288867	intron-variant	NUP153	GRCh38.p7	6:17649313	TTCCTAAAACATAAC[A/G]TGTTGCATGATATAT	9972
rs369751640	snp	A/C	1.65072e-05	0.00287286	missense	NUP153	GRCh38.p7	6:17616678	TTGTAGTGCTGCTGC[A/C]AAACTGGAAAGCCGA	9972
rs369756431	snp	C/G/T	0.00239393	0.0345281	intron-variant	NUP153	GRCh38.p7	6:17661832	TATTGTGGTCCATAA[C/G/T]TTGTTAACTAGAACT	9972
rs369791577	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17685127	CAGTATGTGCAAAGT[C/G]CAATAAAATATGTAT	9972
rs369800643	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692112	TTGGCTCCACCCTCA[C/T]TCATAGATCCCTCAT	9972
rs369887877	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648884	CATTGAGTGCACTCC[C/T]ACCCAAAAAGCATCT	9972
rs369895960	snp	C/T	1.65425e-05	0.00287593	missense	NUP153	GRCh38.p7	6:17675527	TCAAGAATACCTTTA[C/T]CAGAAGCTCTTGAAG	9972
rs369927781	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707964	TTACTATAAATCTTT[G/T]TTTTTCTTTCTTTCT	9972
rs369958788	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17640794	GCTCATTTTTTTTTT[-/T]ACTTTTTTGTAGACA	9972
rs370120523	snp	A/G/T	8.65125e-05	0.00657645	intron-variant	NUP153	GRCh38.p7	6:17665216	CAATATTCAAAGACT[A/G/T]GTAGAAATATACATA	9972
rs370146755	snp	A/G	0.000435832	0.0147555	intron-variant	NUP153	GRCh38.p7	6:17688358	AATTAGGGCATGAAA[A/G]CCTATCATTCATGAC	9972
rs370190728	snp	C/T	1.66181e-05	0.00288249	intron-variant	NUP153	GRCh38.p7	6:17675801	TTAATATTATGAATA[C/T]ACAACTTAGAGCGAT	9972
rs370206461	snp	A/G/T			intron-variant	NUP153	GRCh38.p7	6:17692231	CTTAGATTACAGACC[A/G/T]ATTTTCTATACTAAA	9972
rs370216894	snp	C/G	0.000153988	0.00877328	intron-variant	NUP153	GRCh38.p7	6:17637104	AGAATAAATTAAACT[C/G]TTCAACAGAAGTAAT	9972
rs370220295	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17656963	TTTCAGTCAGTTTTG[C/T]TATCTTGCAAGTGGA	9972
rs370224711	snp	C/T	1.64974e-05	0.00287201	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639967	AATATCTAGAACACT[C/T]CCTTCTTTCAGGATT	9972
rs370264601	in-del	-/GG			intron-variant	NUP153	GRCh38.p7	6:17618701	TCCTGAGTAGCTGGG[-/GG]ACTACAGGCGCCCGC	9972
rs370306145	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17621052	CCCACTGAAAAGCGG[G/T]CAAAGGATCTGAACA	9972
rs370325454	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658632	ACGTTAGCCATTCTA[C/T]GGTCATTCACCATTT	9972
rs370337967	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17646269	CTGGAGTGCAGTGGC[A/G]CAATCCTGGCTCACT	9972
rs370340786	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692526	AAAAACAAAAAGACA[A/G]AAAGAAAGGAGGGAG	9972
rs370348796	snp	C/T	1.66076e-05	0.00288158	synonymous-codon	NUP153	GRCh38.p7	6:17625809	TTTTGTAAATGTACC[C/T]GCAGAGCTAGATGTG	9972
rs370382318	snp	A/G			synonymous-codon	NUP153	GRCh38.p7	6:17637339	CCGAAACCACTGTCA[A/G]TGTAAGGGCTCGCTT	9972
rs370387121	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17623000	CCAGGTGTGGTGGCA[C/T]GTGCCTGTAGTCCCA	9972
rs370406909	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17618061	CCAATCTTAGCTCCC[-/C]AGAACACTGGCAAAT	9972
rs370408157	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17664723	TAAACAATGGGTACA[C/T]GCTAGAGTTTACTAG	9972
rs370415389	snp	A/C	8.34202e-05	0.0064578	intron-variant	NUP153	GRCh38.p7	6:17674887	AAAAAGATCATCAAC[A/C]CTTCTATTGGAACCT	9972
rs370416278	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17675511	TATGTACTACCACAT[A/G]TCAAGAATACCTTTA	9972
rs370438253	snp	A/G	0.000153988	0.00877328	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632691	TTTGCACTTTCACAT[A/G]CCAAACATTTGGTAG	9972
rs370442543	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17674745	CCACCGCACTCCAGC[A/C]TGGGCGACAGAGCCA	9972
rs370457297	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17625516	GCCTGGGTGACAGAG[C/G]AAGACTCCGTCTCGA	9972
rs370458132	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672069	AACAAGCCAATTTTA[G/T]ATTTTTATAGAAAAG	9972
rs370471566	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17658207	TTCAAGACCAGCCTG[-/G]TCAAGATGGTGAAAC	9972
rs370509475	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655229	TTTTAGAATCCAGGA[C/T]AAGGTGAAAGGTAAA	9972
rs370541465	snp	C/T	0.000300393	0.0122518	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632610	GGCCTTACAAAAAGG[C/T]GCTTTACCATCACCT	9972
rs370569267	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17629713	ATATTTAGTCGGTAT[A/G]AGAATGATATCTCAA	9972
rs370675274	snp	C/G	3.30306e-05	0.00406377	missense	NUP153	GRCh38.p7	6:17629165	ATTTGGGCAGTTCCT[C/G]TTTCTTTTCTTCCTG	9972
rs370694775	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708011	GAGAGACAGAGTCTT[A/G]CCCTGTCGCCCAGGC	9972
rs370750802	snp	A/G	0.00013222	0.00812972	intron-variant	NUP153	GRCh38.p7	6:17646192	TATACTTCGTTTTCA[A/G]TAAGTATCAAATATA	9972
rs370816153	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17632871	AAAAAAAACGGGGAG[G/T]GGGGGGAGATTTCAT	9972
rs370850360	in-del	-/AACT			intron-variant	NUP153	GRCh38.p7	6:17697832	CTATTCTATAACACT[-/AACT]CAGAACTCACTTGTA	9972
rs370851290	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641333	CGAGGTCAAGAGATG[A/G]AGACCATCCCGGCCA	9972
rs370859575	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698477	GGCGTGGTGGCTCAC[A/G]CCTGTAACCCCAGCA	9972
rs370863763	snp	C/T	6.59185e-05	0.00574064	synonymous-codon	NUP153	GRCh38.p7	6:17662041	TTGTTCTCTATTTTG[C/T]CCGGGTGTCATATTT	9972
rs370880717	snp	C/T	3.32105e-05	0.00407482	synonymous-codon	NUP153	GRCh38.p7	6:17629307	GGGCTTAGATTCAGA[C/T]GAAACTCCAAATTTA	9972
rs370934028	snp	A/C	3.32193e-05	0.00407536	missense	NUP153	GRCh38.p7	6:17629316	TTCAGATGAAACTCC[A/C]AATTTAAAATCTCCT	9972
rs370950237	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17687541	CTAAGAAAAATTAGG[G/T]TTGCCATTTCTCTAA	9972
rs371024688	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690134	GAGGTAAGTGGATCA[C/T]GAGGTCAGGAGATTG	9972
rs371048454	snp	A/C	0.0254411	0.109879	intron-variant	NUP153	GRCh38.p7	6:17702933	GGCCGGGCGCGGTGG[A/C]TCACGCCTGTAATAC	9972
rs371103219	snp	A/G	3.30568e-05	0.00406538	missense, intron-variant	NUP153	GRCh38.p7	6:17640052	GTACTGTTCACTGTA[A/G]TGACATGATGAGCTG	9972
rs371110683	snp	A/G	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17646309	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	9972
rs371132873	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17616399	TATAGTATGGTAAAT[C/T]TATGTTGGAGAACAT	9972
rs371168350	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17678625	TTTGCCATTCTGTAG[C/T]GTTCTTCTATGTGCT	9972
rs371189089	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17621615	CAAAGACACATATTC[A/C]ATGTTCTCACTCATG	9972
rs371195705	snp	G/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704199	CTGGAGGCTGAGGCA[G/T]GAGAATGGCATTAAC	9972
rs371206009	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17652897	AGCTGGGCGTGGTGG[C/T]GCACACCTGTAATCC	9972
rs371218363	snp	A/G	0.000122602	0.00782852	intron-variant	NUP153	GRCh38.p7	6:17646180	AAAGAATATCCTTAT[A/G]CTTCGTTTTCAATAA	9972
rs371220380	snp	A/G	0.000448492	0.0149681	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706259	CCGCCAGGCCACCGC[A/G]GCGTCGGGGTCCCAT	9972
rs371254767	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17703999	TCTAAGTACATTTAA[A/G]CTGTGATCAGGGGCC	9972
rs371255003	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17686062	CTGAGGTGGGAGGAT[C/G]GCTTGAGCCTGGAAG	9972
rs371255123	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17642166	TAGCTTCAAGACCAT[C/G]GATTTGGCAATGTAT	9972
rs371263282	snp	C/G	9.88468e-05	0.00702948	missense	NUP153	GRCh38.p7	6:17688454	AGTAATATTAGAGCT[C/G]TCCTCATCGGCATAT	9972
rs371305630	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17622403	CCAGCAGGTTGAGGC[A/G]GTAGTGAGCCGAGAT	9972
rs371328183	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17648679	GTGGTGGTGTACACC[G/T]GTAGTCCCAGCTACT	9972
rs371432886	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618787	TAGCCAGGATGGTCT[C/T]GATATCCTGACCTCG	9972
rs371438976	in-del	-/CAAA			intron-variant	NUP153	GRCh38.p7	6:17641568	AAACAAACAAACAAA[-/CAAA]AAGGCCAGGCAGCGG	9972
rs371451392	snp	A/G			downstream-variant-500B	NUP153	GRCh38.p7	6:17614594	GGTTCTGCAGGGTCC[A/G]CTGCTGAAATTTGTG	9972
rs371492077	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679965	ACTCAAGGTAATCAT[C/T]GCAACCAGATATGCT	9972
rs371627499	snp	A/T	1.64906e-05	0.00287142	missense	NUP153	GRCh38.p7	6:17626033	ACTGTCCAAACACAA[A/T]GGTAGCCACAGGTGG	9972
rs371669562	in-del	-/TTGA			intron-variant	NUP153	GRCh38.p7	6:17669745	AATCCAATTCTCTGA[-/TTGA]GAAATTACCTTTACA	9972
rs371772324	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17669081	GTTATGAAAAATACC[-/T]TTTTTTTTTTTTTTT	9972
rs371775093	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644901	CCATCCGAGCTAACA[C/T]GTTGAAACCCTGTCT	9972
rs371794099	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17681387	GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAG	9972
rs371819634	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638337	GAATGACTTTTGTAA[C/T]TGTTTACTTAGGACC	9972
rs371895707	snp	A/G	6.69254e-05	0.00578431	intron-variant	NUP153	GRCh38.p7	6:17647952	AAAAGAGCTTTTTAG[A/G]AAAATAAAGTGACAA	9972
rs371900590	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17694432	CGGAGGCCGACGCGG[A/G]CGGATTACCTGAGGT	9972
rs371987520	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17680125	CCTTGAGCCTCACCT[C/T]CACTGTTTCCCTTGC	9972
rs372015889	snp	A/C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622443	GTACTCCAGTTTGTG[A/C/T]GGCAAGGTGAGACCC	9972
rs372031450	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639629	CAGTTCAGTGCTCTC[A/G]TAAGAGAAAGACATG	9972
rs372040096	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619690	AAATGTAAAGACATC[C/T]TATATTCATGGATCA	9972
rs372055394	snp	C/T	0.000214145	0.0103454	synonymous-codon	NUP153	GRCh38.p7	6:17688562	CTTGTTGAAGTATCT[C/T]TGTAGCCACCCTGGC	9972
rs372084684	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17655136	TTTTAACAACACACA[-/C]CAAAAAAACTCATGG	9972
rs372095851	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17650577	TTATTGCAAATAAAT[A/C]ACAGCTCAATAAAAT	9972
rs372098303	snp	A/C	1.64827e-05	0.00287073	synonymous-codon	NUP153	GRCh38.p7	6:17688592	CACAATATTCTTAAC[A/C]GATTCTGTAACCCTG	9972
rs372107673	in-del	-/A/AA/AAA/AAAA	0.65186	0.120138	intron-variant	NUP153	GRCh38.p7	6:17669031	CCTATCAAGAGGCTG[-/A/AA/AAA/AAAA]AAAAAAAAAAAAAAC	9972
rs372112061	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674581	TCAAGACCATCCTGG[C/T]CAACACAGTGAAACC	9972
rs372121201	snp	A/C/G	4.94444e-05	0.00497194	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616088	TTGAGTACAACACCA[A/C/G]TGTGACCTTTATTTC	9972
rs372140662	snp	C/T	1.73881e-05	0.00294852	missense	NUP153	GRCh38.p7	6:17629533	GATGAGGAAGATGTG[C/T]CAAAGCCTACAAAAA	9972
rs372167764	snp	C/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17694256	AGAATAGTAATGTTT[C/G]CCTTTACCTCCATGA	9972
rs372168351	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698598	AAAAAATTAGCGGGG[C/T]GTGGTGGTGGGCACC	9972
rs372173889	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17641859	TGTCTCAGAAAAAAA[-/G]AAGAAAGAAAAAGAA	9972
rs372212025	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17661293	CACTCCAGCCTGAGC[A/G]ACAGAGCAAGACTGT	9972
rs372212996	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17645029	GGCGGAGGTTGCAGT[A/G]AGCCAAGATTACGCC	9972
rs372229723	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17623761	AAACAATCACAAATC[A/T]AAAGACTGCATGCAG	9972
rs372265601	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17639117	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	9972
rs372278441	snp	A/G	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17649201	AATTGATGGGTGATG[A/G]AGAGGAAGTTGTGAT	9972
rs372282725	snp	C/T	3.80945e-05	0.00436415	missense	NUP153	GRCh38.p7	6:17628691	CTCCAAAGGCAAAAG[C/T]GGCTTTTGCTGGCTG	9972
rs372309593	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685217	TCCAGAATCTGACAC[C/T]ACTTCAACAGCAGAT	9972
rs372361816	snp	A/C/G	0.000206627	0.0101624	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706391	TCCCGAGGCCATGGC[A/C/G]GAGCCTCCGCCGCTT	9972
rs372418341	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17645362	GTGGTAGTGCAATCA[C/T]AGCTCACTGTAGCCT	9972
rs372476990	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17697681	CGACTGAGCGAGACT[C/G]CATCTCAAAAAAAAG	9972
rs372478786	snp	A/G	6.92761e-05	0.005885	intron-variant	NUP153	GRCh38.p7	6:17668949	TTGTAGACAGTTTAA[A/G]TAACTAAATGCTAAA	9972
rs372479573	snp	A/G	0.000153988	0.00877328	intron-variant	NUP153	GRCh38.p7	6:17669274	AATATTTTGTAAAAA[A/G]GTTTAAATCTCAACT	9972
rs372513832	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671711	TCTTTAGACTCAAAT[A/G]CAATCTCAATCATGG	9972
rs372518303	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17657764	AAAAATAAGCTCATG[C/G]TATATGAATCAGATA	9972
rs372565692	in-del	-/GAACCCGGGT			intron-variant	NUP153	GRCh38.p7	6:17690297	CGTAGCTTGCAGTGA[-/GAACCCGGGT]GCCGAATGTGCAGTA	9972
rs372595606	snp	C/T	4.94205e-05	0.0049707	missense	NUP153	GRCh38.p7	6:17637503	GCAGAAAGAGTTGTT[C/T]TGCCACTTTTATTTG	9972
rs372605064	snp	G/T	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17675287	TTTGAGCTGGTGGCA[G/T]TGTGCTGTGAGAGTG	9972
rs372608494	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619905	GAGTTCGAGACCAGC[A/G]TGGCCAACATGGCAA	9972
rs372653572	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17670442	CTTTTTTTGTATTTT[-/C]TTTGGATTTTTCTAC	9972
rs372696009	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679236	AAAAATGTGTTTCTA[A/G]GCACTAATAATGAAC	9972
rs372733612	snp	C/G	0.000100519	0.00708869	intron-variant	NUP153	GRCh38.p7	6:17665236	AAATATACATATACT[C/G]ACACTGCACTTGTTA	9972
rs372751834	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667485	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	9972
rs372754447	snp	A/G	3.34258e-05	0.00408801	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706305	CGCCCCTGCTGGTAA[A/G]GCTTAATTGGCCCCT	9972
rs372762815	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655883	AACTATATAATTGTG[C/T]ATCCAAACCTATTCT	9972
rs372772287	snp	C/T	1.65455e-05	0.00287619	synonymous-codon	NUP153	GRCh38.p7	6:17616691	GCCAAACTGGAAAGC[C/T]GAACCTGCAATAGTT	9972
rs372785560	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17616785	GACGGAGTCTCGCTC[C/T]CTTGCCCAGGCTGGA	9972
rs372837545	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630638	ACAGCACTCCAGCCC[A/G]GTCAACAGTGAGACT	9972
rs372841653	snp	C/T	7.22113e-05	0.00600836	intron-variant	NUP153	GRCh38.p7	6:17637798	AAGGAGAGAGTGCAA[C/T]GTTAGAGAAGCTTTA	9972
rs372866124	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660490	AATCTTAAATCTGTC[C/T]CTATCTTTTCCAAAC	9972
rs372868015	snp	A/G	6.78242e-05	0.00582301	missense	NUP153	GRCh38.p7	6:17637758	ACAGAATCTATCTTC[A/G]GCGATGCGAAACCTA	9972
rs372886342	snp	C/T	1.66418e-05	0.00288455	intron-variant	NUP153	GRCh38.p7	6:17675816	TACAACTTAGAGCGA[C/T]ACACTACCACAAATG	9972
rs372894597	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17630144	TATGTTTGCCTTGGA[A/T]GGGCATAAAGAAACT	9972
rs372996702	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17682752	TGAAACCCCATCTCT[A/C]CTAAAAATACAAAAA	9972
rs373003329	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17645700	TTGTGAACTGAAAGG[C/T]AAAAACTAGAAATAA	9972
rs373041462	in-del	-/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17697815	GCTGGGGTGGGGGAA[-/G]GCTATTCTATAACAC	9972
rs373052717	snp	G/T	1.66054e-05	0.00288139	missense	NUP153	GRCh38.p7	6:17624773	GTTGGGGTCTGGTTA[G/T]CACCAAATGCTGGAC	9972
rs373125087	snp	A/G	8.24545e-05	0.00642032	intron-variant	NUP153	GRCh38.p7	6:17661991	GTTAAATATAAAGAA[A/G]TATAGCTGTATAAGA	9972
rs373135672	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17640473	GCAATTATTTCATTT[C/T]TAGAAATTCACACTA	9972
rs373172405	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17682528	ATCCTCTCAAATTTC[A/G]CTGCTGCTTTATCAA	9972
rs373182328	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17703386	GCACTGGCAAACATC[C/T]ATTAACTAACAGCGC	9972
rs373184539	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17662652	ATACTTATTCATTAC[A/G]AAAGGTAAAATAGTA	9972
rs373196566	snp	C/T	1.69844e-05	0.00291409	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706357	TCTTGCCGCCACCGC[C/T]CCCTCCGACTCCTCC	9972
rs373215207	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17676436	TAAATATTATGCTTT[A/T]GAATTTAATGCGTGT	9972
rs373234983	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685375	ACACGGAGAAACCCC[A/G]TCTTTACTAAAAATA	9972
rs373244830	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620928	AGGAGTGAAAAATTT[A/G]TTGAAAGGGAAAAAA	9972
rs373304323	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685744	AGCAAATACATTTAT[A/G]TACTCTATAGAATAC	9972
rs373307370	snp	A/C/T	9.90662e-05	0.00703735	missense	NUP153	GRCh38.p7	6:17675744	ACACATCTGGATAAT[A/C/T]TGAAGCAGTACTAGT	9972
rs373316698	snp	C/T	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17667880	TAAGCAAATAGGATA[C/T]ATTAAAAGGGCAGCA	9972
rs373322315	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17650392	CAAAGTCTACATATA[A/C]GCCACCCGAATCTCT	9972
rs373329637	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630762	AGAAGGGAGGGGAGA[A/G]GGGAGAGGGGAGAGG	9972
rs373401061	snp	A/G	0.000214516	0.0103543	missense	NUP153	GRCh38.p7	6:17629155	GCAGAGGAAGATTTG[A/G]GCAGTTCCTCTTTCT	9972
rs373407975	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17644270	CTTTTCGATAAGGTA[A/G]TATCTCCCAACTCAT	9972
rs373410612	in-del	-/TCTAATCTATACAGAAT	0.0252325	0.109451	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615673	TCCGTTTCAACACTC[-/TCTAATCTATACAGAAT]TCTAATCTATACAGA	9972
rs373417963	snp	G/T	1.64806e-05	0.00287054	synonymous-codon	NUP153	GRCh38.p7	6:17669478	CAATATTCGCCGAGC[G/T]GTTGAACTGGTCACA	9972
rs373419439	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17675466	CAAGTCAGAAAAAAA[A/C]CCCATAAAATTTAAT	9972
rs373424400	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17645312	TCTTTCTTTTTTTTT[-/T]GAGATAGGGTCTTGC	9972
rs373468109	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17699718	CACACACCTGTAACC[C/G]CAGTTACTCAGGAGG	9972
rs373481518	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17663755	ATAAAATATAACTAA[A/C]GGCATAAACAATAAG	9972
rs373516317	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17658360	GAGATCATGCTACTG[A/C]CCTCCAGCCTGGGCC	9972
rs373519975	snp	A/C/T	6.92455e-05	0.00588378	intron-variant	NUP153	GRCh38.p7	6:17637777	ATGCGAAACCTACAA[A/C/T]GAACGAAGGAGAGAG	9972
rs373576612	in-del	-/A	0.0399052	0.1355	intron-variant	NUP153	GRCh38.p7	6:17682240	ACAACATACCTACTT[-/A]AAAAAAAAATTGCTA	9972
rs373664481	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17687289	AACCAAAAGGAAACA[A/G]ATCTCATAACCAGGA	9972
rs373666192	snp	A/C			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705430	GGCTAAACTATAAGA[A/C]CACCAACATTCCTGG	9972
rs373673208	snp	A/C	0.000153988	0.00877327	missense	NUP153	GRCh38.p7	6:17629311	TTAGATTCAGATGAA[A/C]CTCCAAATTTAAAAT	9972
rs373691457	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17616338	TACACCTAACACACA[C/T]GCTACTGTTATTTTT	9972
rs373714160	snp	C/T	0.00023062	0.0107358	missense	NUP153	GRCh38.p7	6:17647848	CAGTAGATTTTACGA[C/T]TGGAGATGAAAATTT	9972
rs373841413	in-del	-/A	0.348794	0.229651	intron-variant	NUP153	GRCh38.p7	6:17685549	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	9972
rs373891082	in-del	-/C			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705844	AAGGGGCAGCCCCCC[-/C]TCCTCAAACACACTA	9972
rs373895949	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672135	AGAACAAAATTGGAC[C/T]ACTCACATCACCTAA	9972
rs373945087	snp	A/G	1.75767e-05	0.00296446	intron-variant	NUP153	GRCh38.p7	6:17640111	CCAAATAAAACACTG[A/G]ACTCTCAAATGCATT	9972
rs373945530	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17662166	AATATTTAGAATCAG[A/G]AATTTGATGGCTTTT	9972
rs373960251	snp	C/G	0.000153988	0.00877327	intron-variant	NUP153	GRCh38.p7	6:17646027	CTAATCTACTGTATG[C/G]AATTGTTTGTATGTT	9972
rs373974946	snp	C/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706856	CGTCGTCGTCGTCGT[C/G]CCTGCAGCCTCCGCC	9972
rs374061375	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688845	AATTGTCCCAAATGG[C/T]TGCATTATTCTAATC	9972
rs374084765	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695598	GAGTTGATTTCCACC[A/G]TTAAAGACTTACACA	9972
rs374120509	snp	C/T	0.000182945	0.00956236	intron-variant	NUP153	GRCh38.p7	6:17669564	GTAAAGTAAACCCTA[C/T]ATTATTTGTTGCAAC	9972
rs374127744	snp	A/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637408	ATTTTATTGCTTCAG[A/G]TTTATTTTGCACTAA	9972
rs374130734	snp	A/G	1.64925e-05	0.00287158	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632673	CCAGATTTTGTGCCT[A/G]GCTTTGCACTTTCAC	9972
rs374223182	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17647521	GCTGTATTGTGGGGA[G/T]GCAAAGGAATGTCTT	9972
rs374231956	snp	A/T	3.38541e-05	0.00411411	intron-variant	NUP153	GRCh38.p7	6:17624519	AATATTTTAAGACAC[A/T]CAAAACCCATACAGA	9972
rs374301711	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17699481	GGGCGAGACTCGTCT[A/C]AAAAAAAAAAAAAAA	9972
rs374310449	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677927	TTAACTTTGTGTCAA[C/T]TGCTAGAGTTTTCTT	9972
rs374329933	snp	A/G	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17625880	TACTGCTGGCTCCTG[A/G]ACCAAAGACAAATGG	9972
rs374331301	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17669225	CTGGGACTACAGGTG[A/T]GCACCACCACACCCG	9972
rs374360029	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17650619	CCCAAAGCAAAATAA[-/A]GGCACTTCCAGATAA	9972
rs374425673	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17638482	TCTAGTTCCACAAAA[A/T]AATCCAGCCTAGAGC	9972
rs374644758	snp	C/T	1.64988e-05	0.00287213	missense	NUP153	GRCh38.p7	6:17688608	GATTCTGTAACCCTG[C/T]TAAGAATGCCCTGTT	9972
rs374697080	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17663233	TAAAAAGAAAAAAAT[-/A]CACACACACACACAC	9972
rs374701160	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17623791	GTAATATTCCATTTA[C/T]ATAAAAGCAGGCAAA	9972
rs374756705	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17651348	TTATAATAATAAATA[C/T]TAAATAATTAAATAA	9972
rs374767863	snp	C/G	2.05413e-05	0.00320472	intron-variant	NUP153	GRCh38.p7	6:17646181	AAGAATATCCTTATA[C/G]TTCGTTTTCAATAAG	9972
rs374785160	snp	C/T			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707001	AAGAGGAAGGGCTGG[C/T]CGAGTCCACGCTCTC	9972
rs374794485	in-del	-/GACA			intron-variant	NUP153	GRCh38.p7	6:17642378	ACTCAGTAACAAAAA[-/GACA]AACTGTTCAATGGGT	9972
rs374901950	snp	A/G	4.94539e-05	0.00497238	synonymous-codon	NUP153	GRCh38.p7	6:17616175	GAACACATTTTTCCC[A/G]TTTGACCTGTGAAAA	9972
rs374935354	snp	C/T	1.64901e-05	0.00287137	missense, intron-variant	NUP153	GRCh38.p7	6:17640035	GTGTCTTCTTACAAT[C/T]TGTACTGTTCACTGT	9972
rs374947018	snp	C/T	3.29565e-05	0.00405921	missense	NUP153	GRCh38.p7	6:17629093	TCACTATGGTGTTAG[C/T]AGGAGCAGGGGTGGA	9972
rs375011488	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17645434	AGGTAGCTGGGACTA[C/T]AGGCTCACACCACCA	9972
rs375063087	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17677844	TTGATATTACAAATG[C/G]GATCCTTTCTTCTTT	9972
rs375112063	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646427	TAGCCAGGATGGTCT[C/T]GATCTACTGACCTTG	9972
rs375150676	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17702493	AGCCTGGGTGACAGA[C/G]CGAGACTCTGTCTCA	9972
rs375177320	snp	A/G	5.1522e-05	0.00507527	intron-variant	NUP153	GRCh38.p7	6:17668965	TAACTAAATGCTAAA[A/G]AAGTTTTACCTTTTC	9972
rs375188251	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17643480	CACCCACCCCCAACC[A/T]TCCCCACCAAAAATA	9972
rs375244755	snp	A/C/G	0.000263975	0.0114859	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616057	TCTGAAAGCAGGGCA[A/C/G]CAGCTGTTGTTAAAA	9972
rs375321404	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17685022	CAAGAATTACCAAAG[C/T]GACAGACATGTTAGC	9972
rs375323904	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17668853	GACTCAAAAAAAAAA[-/A]GAATATTATTTTTCA	9972
rs375330045	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648849	GATGTTACGCCTAGC[C/T]GAGAAGTAAAAACAT	9972
rs375337834	snp	A/C	0.000138048	0.00830691	intron-variant	NUP153	GRCh38.p7	6:17675415	ACACCAATACAAGAG[A/C]CTAGATTTTTATAAA	9972
rs375382666	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17691040	CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAAAAT	9972
rs375419681	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698655	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	9972
rs375427965	in-del	-/AAAC	0.0275645	0.114116	intron-variant	NUP153	GRCh38.p7	6:17641545	CTCAAAAACAAAACA[-/AAAC]AAACAAACAAACAAA	9972
rs375498574	snp	C/T	8.2528e-05	0.00642318	missense	NUP153	GRCh38.p7	6:17625826	CAGAGCTAGATGTGG[C/T]TGTGGCTCCAAAGCC	9972
rs375565425	snp	C/G	3.29853e-05	0.00406098	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632800	AGCCTCCAGAAGGCA[C/G]AGAGACAGGTACAGT	9972
rs375590903	snp	A/C/G	5.30171e-05	0.00514837	intron-variant	NUP153	GRCh38.p7	6:17688348	GTGTCTTCAAAATTA[A/C/G]GGCATGAAAACCTAT	9972
rs375598642	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640577	GGTTACATAAATTAC[A/G]TAACAGTGACATGAT	9972
rs375676599	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17668830	TCTGGATGACAGAGC[A/G]AGACTGAGACTCAAA	9972
rs375679255	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631884	AAGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	9972
rs375684502	snp	A/C/G	4.97305e-05	0.0049863	missense, intron-variant	NUP153	GRCh38.p7	6:17640059	TCACTGTAGTGACAT[A/C/G]ATGAGCTGTAATTTT	9972
rs375746558	snp	C/T	4.98194e-05	0.00499071	missense	NUP153	GRCh38.p7	6:17629312	TAGATTCAGATGAAA[C/T]TCCAAATTTAAAATC	9972
rs375793789	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17643779	AGGCCACTCATAATC[C/G]ACTCCTTAAAAATCT	9972
rs375853231	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17681594	TCTCAAAACAAAACA[A/C]AAATAAAAAACCAGA	9972
rs375854314	snp	G/T	2.07648e-05	0.0032221	intron-variant	NUP153	GRCh38.p7	6:17632879	CGGGGAGTGGGGGGA[G/T]ATTTCATGAAAATTT	9972
rs375866144	snp	C/G/T	3.32802e-05	0.00407912	missense	NUP153	GRCh38.p7	6:17669294	AAATCTCAACTTACA[C/G/T]AATTCAGAGGAGAAG	9972
rs375875659	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688336	CATAACTAGGTAGTG[C/T]CTTCAAAATTAGGGC	9972
rs375898668	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17656407	GAGGGGAGGAGGTGA[C/T]ACAAACATGAGTGAA	9972
rs375926589	snp	C/T	8.24015e-05	0.00641825	synonymous-codon	NUP153	GRCh38.p7	6:17625950	GCTATCTTGAGAAAA[C/T]AGCAAAGACTGAGAG	9972
rs375949839	snp	A/C	3.3579e-05	0.00409736	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706334	CTGGTGGCAACGCCG[A/C]GTCCGGATCTTGCCG	9972
rs375977253	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17623061	CTTGAACCCGGGAAG[C/T]GGAGGTTGCAGTGAG	9972
rs375991656	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17616972	GGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT	9972
rs375994739	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17665052	AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAATT	9972
rs376029654	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17691833	AGAATTTTTTTTTTT[-/T]CCAGAGACCTGTGTC	9972
rs376029811	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696121	TGACAAGAGTGAAAC[C/T]GTCTCAAAACAAACA	9972
rs376031078	snp	C/T	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17674909	TTGGAACCTACCTGA[C/T]AAGGTGTATTTCGTA	9972
rs376077706	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17630702	GGAGAGCAGAGGAGA[C/T]GGGAGACGAGAGGGG	9972
rs376131066	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676437	AAATATTATGCTTTA[A/G]AATTTAATGCGTGTT	9972
rs376158583	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697503	CAAGCCTGGCCAACA[C/T]GGCGAAACCCTGTCT	9972
rs376202268	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679143	TGATATAATCTTACA[C/T]GTAAATAACAGTGAA	9972
rs376214373	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641315	GCCAAGGCGGGCAGA[C/T]CACGAGGTCAAGAGA	9972
rs376217772	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620384	TGATGACAAGAACAC[A/G]CATTGGGAAAAGGAT	9972
rs376219935	snp	A/G	1.64882e-05	0.00287121	intron-variant	NUP153	GRCh38.p7	6:17661996	ATATAAAGAAGTATA[A/G]CTGTATAAGAAATGA	9972
rs376244443	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17646918	TAATTCTGTATTTTC[-/T]TTTTTTTTTTTTTTT	9972
rs376259498	snp	G/T	6.58979e-05	0.00573974	missense	NUP153	GRCh38.p7	6:17637230	ACTGAACACTCCCAA[G/T]ATCCAATGGGCCTTT	9972
rs376279477	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690563	TAACAGAAACATACT[A/G]AAAACTTTTTTACTA	9972
rs376294465	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17699338	CGTCCCTACTAAAGA[A/T]ATAAAAACTTAGCCA	9972
rs376299910	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17704018	TGATCAGGGGCCGGG[A/C]GCGGTGGCTCACGCC	9972
rs376308519	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17643665	AAACTTAGCTCCTGT[C/G]ACAAAGTAATCATGA	9972
rs376320270	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643171	TATCATGTCAACTTC[A/G]TCACAATAACAAAAA	9972
rs376348557	snp	A/G	1.99798e-05	0.00316062	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706403	GGCGGAGCCTCCGCC[A/G]CTTCCCGCTCCGGGG	9972
rs376386030	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17649871	ATTATCTGCAGTTTC[A/G]GGTATGACCTGGGAT	9972
rs376395961	snp	G/T	3.29788e-05	0.00406058	synonymous-codon	NUP153	GRCh38.p7	6:17669505	CACACCGTAAGATTG[G/T]GCACTGAGTTGCTTA	9972
rs376450981	snp	C/T	0.000255065	0.0112902	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632633	CATCACCTTTATTTT[C/T]ATTTTTTTGGCCTTA	9972
rs376507775	snp	A/C	0.000153988	0.00877328	missense	NUP153	GRCh38.p7	6:17675011	AGCTGACTGGTTTTA[A/C]GGATTGAAGAATTCC	9972
rs376508281	snp	C/T	3.30246e-05	0.0040634	missense	NUP153	GRCh38.p7	6:17629162	AAGATTTGGGCAGTT[C/T]CTCTTTCTTTTCTTC	9972
rs376518859	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620982	AGGGGACTAATATCC[A/G]GAATACACAATGAGC	9972
rs376521486	snp	C/T	9.88761e-05	0.00703052	missense	NUP153	GRCh38.p7	6:17669480	ATATTCGCCGAGCTG[C/T]TGAACTGGTCACACC	9972
rs376529976	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706894	CGCCTATTACCCCTG[A/C]TAAGGCGGCTGCCGC	9972
rs376557357	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672148	ACTACTCACATCACC[C/T]AATTTTAAGACCTAC	9972
rs376584046	snp	C/G	1.65551e-05	0.00287702	missense	NUP153	GRCh38.p7	6:17675767	GTACTAGTTGTTGAA[C/G]GTTCTTAAAAGAAAA	9972
rs376619096	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17632164	AAGTTCATCTGGGCG[C/T]GGTGGCTCACACCTG	9972
rs376657928	snp	A/C	1.77571e-05	0.00297964	intron-variant	NUP153	GRCh38.p7	6:17669040	GAGGCTGAAAAAAAA[A/C]AAAAACACTATTAGA	9972
rs376726320	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17649531	TTCCTAATTGGTAAA[-/A]CTGAGGGAAAAAAGA	9972
rs376748184	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671730	TCTCAATCATGGCTG[A/G]GCATGCTGGCTCATA	9972
rs376753315	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654095	CTACTGTGTGTATAC[A/G]CTGCACAGTTCTTTC	9972
rs376755459	snp	A/G	3.48985e-05	0.00417709	intron-variant	NUP153	GRCh38.p7	6:17637782	AAACCTACAATGAAC[A/G]AAGGAGAGAGTGCAA	9972
rs376767108	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617266	GAAATCAACAAATAC[A/G]CTTAGCTCTATCTTC	9972
rs376800994	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642378	ACTCAGTAACAAAAA[A/G]ACAAACTGTTCAATG	9972
rs376815098	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682683	CAGCACTTCGGGAGG[C/T]TGAGGGGTGCAGATC	9972
rs376856171	snp	C/T	0.00676609	0.0577691	intron-variant	NUP153	GRCh38.p7	6:17694541	TGATGCCTGTAATCC[C/T]AGCTACTCAGGAGGC	9972
rs376860843	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657844	CTTGATAATTGGAAT[A/G]CATTCTTAAATGTGG	9972
rs376986136	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633792	TCGCCACCTCTTCCA[C/T]AGTTACCTAACTGAT	9972
rs376991640	snp	C/T	1.72291e-05	0.002935	intron-variant	NUP153	GRCh38.p7	6:17625772	AATAAGTAAAGTCCA[C/T]CCAATTACAATGCAT	9972
rs377011678	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690107	CCTGTAATCTCAGCA[C/T]TTTGGGAGGCTGAGG	9972
rs377030939	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17676476	TCCACCCCACCTTCC[C/T]GTTATTAAAATATTA	9972
rs377043052	snp	C/T	4.94588e-05	0.00497262	missense	NUP153	GRCh38.p7	6:17625846	GCTCCAAAGCCGAAA[C/T]CAGAGGTGGTAGTAT	9972
rs377048031	snp	C/T	8.98944e-05	0.00670366	intron-variant	NUP153	GRCh38.p7	6:17646021	GAAATACTAATCTAC[C/T]GTATGCAATTGTTTG	9972
rs377105087	in-del	-/CATA			intron-variant	NUP153	GRCh38.p7	6:17663260	acacacacacacaca[-/CATA]TATATATATATAttt	9972
rs377115579	in-del	-/A/AA/AAA/AAAA/AAAAA	0.588234	0.176637	intron-variant	NUP153	GRCh38.p7	6:17628610	AAAACGACAACTTGT[-/A/AA/AAA/AAAA/AAAAA]AAAAAAAAAAATAAT	9972
rs377120023	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17625444	CTGAGGCAGGAGAAT[G/T]GCTTGAACTCGGGAG	9972
rs377128114	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17686398	AACAAACCTTTTTTT[-/T]ATTTCTTTTTTTTTT	9972
rs377258919	in-del	-/TC			intron-variant	NUP153	GRCh38.p7	6:17618557	TAGTGGAAGTTAAAA[-/TC]TCTCTTTTTTTTTTT	9972
rs377303845	in-del	-/A			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704292	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	9972
rs377304074	snp	A/T	0.486067	0.0822953	splice-acceptor-variant, intron-variant	NUP153	GRCh38.p7	6:17632846	AGGTACTGAACTTCC[A/T]AAAAAAAAAAAAAAA	9972
rs377329600	snp	C/G/T	0.000197737	0.00994163	synonymous-codon	NUP153	GRCh38.p7	6:17675643	GCCAATTGGGAATGC[C/G/T]GAGGATGTAGATGGC	9972
rs377387766	snp	C/T			synonymous-codon	NUP153	GRCh38.p7	6:17646143	AACAGGCACACTAAA[C/T]GTAAATCCAATCTGT	9972
rs377396748	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17662663	TTACGAAAGGTAAAA[C/T]AGTAATTTTATAGTA	9972
rs377450834	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17667911	AGATATAATGATCAA[A/C]TTTATCAGTTCCACT	9972
rs377501029	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673402	GACACTGTTAAGATA[C/T]ACCAGAGAATGGGAG	9972
rs377505324	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17635960	CAACTTAAAATTAAT[G/T]TTGCTTTCCTGCATA	9972
rs377528313	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707820	ATGTCCAGAGAAATT[C/T]AGGTGGCACAATCAA	9972
rs377545409	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634802	TAATTTTATGTCCTC[C/T]ATTCCTTATTCAGTT	9972
rs377563094	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17675862	AAACACATTACAGTA[C/T]ATAATAGCTTCAATT	9972
rs377564469	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17650260	TTCCTGTTCTCTTCA[G/T]GAGTTGCTGCCACTG	9972
rs377664157	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17691531	GCACTTTGGGAGGCC[A/G]AGTCTGGTGGATCAC	9972
rs377689236	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17694311	ACCAGGATAAAGACC[-/C]TTTTCTGGTCCATTT	9972
rs377697983	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666793	ATAAAGCCAGAAGCT[C/T]CTAACTCTGTCCAAA	9972
rs386358801	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17623358	AACTGAAAAATGGCC[-/AA]AAAAAAAAAAAAAAA	9972
rs386406292	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17632847	GTACTGAACTTCCTA[-/AA]AAAAAAAAAAAAAAA	9972
rs386406293	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17682941	AAAAAAAAAAAAAAA[-/AA]ACACTTTCTTTGCGC	9972
rs386406294	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17691827	ATAGCAAGAATTTTT[-/T]TTTTTTCCAGAGACC	9972
rs386406295	in-del	-/GCCTGTAATACCAGCACTTTTGGGAGGCTGTGGCGGGTGGATCAC			intron-variant	NUP153	GRCh38.p7	6:17702938	GCGCGGTGGCTCACG[lengthTooLong]CCTGTAATACCAGCA	9972
rs386697561	multinucleotide-polymorphism	CAT/GCC			intron-variant	NUP153	GRCh38.p7	6:17645189	CAGAGGTTGCAGTGA[CAT/GCC]AAGACCGTGCCATTG	9972
rs386697562	in-del	GAA/T			intron-variant	NUP153	GRCh38.p7	6:17683100	CTCCACTGAAGTCCT[GAA/T]CCCCTCAAAGTTATC	9972
rs397760073	in-del	-/A/AT	0	0	intron-variant	NUP153	GRCh38.p7	6:17628621	TTGTAAAAAAAAAAA[-/A/AT]TAATAATAATAATAA	9972
rs397954885	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17616290	GTCGGGTGGGGGGGG[-/G]AGTAGACTCACATTG	9972
rs398000683	in-del	-/A	0	0	intron-variant	NUP153	GRCh38.p7	6:17617486	AAAAAAAAAAAAAAA[-/A]GGATGGCAGAGTATG	9972
rs398000684	in-del	-/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17618582	TTTTTTTTTTTTTTT[-/T]AAAGATGGAGTCTGG	9972
rs398000685	in-del	-/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17634454	ACATTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC	9972
rs398000686	in-del	-/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17654338	ATTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGA	9972
rs398000687	in-del	-/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17677749	TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTC	9972
rs398000688	in-del	-/A	0	0	intron-variant	NUP153	GRCh38.p7	6:17689083	AGTTAAAAAAAAAAA[-/A]TACAGGAACTAAAAC	9972
rs398084789	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17670743	TTTTTAAAAAATATT[-/T]TATGTATCTATAGAG	9972
rs527241101	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637941	ATTTATCAATTACCT[A/C]ATAAGTTACACTTAA	9972
rs527277048	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674773	CCAAGACTCCATCTC[A/G]AAAAAATATAAATAA	9972
rs527302339	snp	A/C	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17674396	ATAAAACACTCACTT[A/C]GGTCTAAAATAATGT	9972
rs527312846	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636734	TGCAACAGCTACAGC[C/T]TTTTCATTAACGACT	9972
rs527321058	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17685549	CAAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	9972
rs527322220	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687896	GAGGCGGATGGATCA[C/T]GAGGTCAGGAGATCG	9972
rs527359515	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17691594	ACATGGCAAAACCCC[A/G]TATCTACTAAAAATA	9972
rs527362186	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677894	TTAAATAAGAGAGTC[A/G]TTAGGTATTTTTCAA	9972
rs527388721	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17656265	AACATCACATTAGTA[C/T]CTCTTTCCTCAGAAA	9972
rs527402383	in-del	-/A	0.0130921	0.0798413	intron-variant	NUP153	GRCh38.p7	6:17638690	ATGAAGATTCTCCCC[-/A]AACATTTCCTATTTA	9972
rs527439027	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17618759	TCTTAGTAGAGATGG[A/G]GTTTCACCGTGTTAG	9972
rs527450467	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17694233	ATCAGCAAGTATTGA[C/T]TGAATGAAGAATAGT	9972
rs527457528	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618733	ACCACGCCTGGCTAA[C/T]TTTTTGTATTTCTTA	9972
rs527473649	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17701108	CGCATGCCTGTAATT[A/C]CAGCTACTTGGGAGG	9972
rs527566445	snp	A/G			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615310	CAACTTTGAATAATG[A/G]GATTTACATAATAAA	9972
rs527570294	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705470	AGTAACTATACTTCT[A/G]GAATACGCCTCATAA	9972
rs527577067	snp	A/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17699259	CCCAACACTTTGGGA[A/G]TCTGAGGCAGGCAGA	9972
rs527620700	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654492	ACGCCCAGCTAATTT[C/T]TGTATTTTTAGTACA	9972
rs527638345	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705057	CCAACGCGCCCGACC[C/T]AAATCTTTACTTTTA	9972
rs527643144	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17645507	TGAGTCTCACTGTGC[G/T]GCCTAGGATCGTCTT	9972
rs527767494	snp	A/G	4.97104e-05	0.00498525	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639943	AATTATCTTACCAGG[A/G]CTTTTCAGAATATCT	9972
rs527831238	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632232	CTTGAACCTGGGAGG[C/T]GGAGATTGCAGTGAG	9972
rs527864868	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17679875	CCAAAATCAAACCAA[A/G]GTTGCAGAGAGTCCA	9972
rs527948583	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17626722	TTATACCATGGACTG[A/T]TATTAGTAGGACAAA	9972
rs527948591	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17670762	GTATCTATAGAGATG[G/T]TCATATAGTACTCTT	9972
rs527982341	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17650022	AACCCAACTGAACAA[A/T]GAGCACCCTAAGTCT	9972
rs528008217	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620305	AAAGACACATAGACC[A/G]ATGGAATAGAATAGA	9972
rs528042218	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698533	CACAAGGTCAGGAGA[C/T]TGAGACCATCCCGGC	9972
rs528052668	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691733	CCTGGGTGACACAGC[A/G]AGACTCCAGCTCAGA	9972
rs528069437	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693802	GAGGCAGAAAAAACG[C/T]TTGAACCCAGGAGGC	9972
rs528110917	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659604	CAGCCTCCCGAGTAG[C/G]TGGGACTACACACAT	9972
rs528126223	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653106	GAAATATAAAAAATT[A/G]GCCGGGCATGGCAGT	9972
rs528167795	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697219	TGGGTATTCTCTCTC[C/T]AAGAAAGAAGGGTTC	9972
rs528168486	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653729	TGATTGCCTCTGGGG[A/T]AGGAGGTGACGGCAA	9972
rs528171294	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646514	CCTGGCCCAAATATA[A/G]AGGTTATTTTTATCC	9972
rs528216437	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17691001	AAAAAAATTAGCCGG[G/T]TGTGGTGGTGTGCAT	9972
rs528221407	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17702737	ATCTAGGCAAAAAGG[G/T]AAAGGGGTAGGGGAG	9972
rs528229304	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647239	CTGGGGCAATTTGAA[A/T]ATTAAACTACGTGTT	9972
rs528243241	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17641506	TGCCACTGTACTCCA[G/T]CCTGGTGACAGAGCG	9972
rs528346401	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17619140	AAGAAACAGGCCAAA[C/G]AGCAAAGATCAAGAC	9972
rs528383527	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678228	GGGCATGGTGGCACA[C/G]GCCTGTAATTCCAGC	9972
rs528394564	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622194	GTAGCTCACGCCTGT[A/G]ATCCTAGCACTTTAG	9972
rs528427547	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627812	TGGCAAATAGCTTTT[C/T]TCTCTGAAAGCATTT	9972
rs528451361	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684390	AATCTCTGCTGGCTT[C/G]CAGCTTTTCTCCTGC	9972
rs528459261	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644401	ATCTCCCTAATGCAG[C/T]CAGAATAAAATCCAA	9972
rs528481531	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628319	GAAAATACTTCATAA[A/G]CTAAGAATCCTTATT	9972
rs528572820	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17667284	TTCCAATAAAAAGTT[C/T]AATATTAGCTTTCTT	9972
rs528587331	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690257	CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA	9972
rs528595502	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660526	TGGTCAGAATATATA[A/G]AGAACTCTTTCTAAT	9972
rs528627980	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616290	GGTCGGGTGGGGGGG[C/G]AGTAGACTCACATTG	9972
rs528643237	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689629	ACAACCTCCGCCTCC[C/T]GGGTTCAATGGATTC	9972
rs528647284	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661209	GTCCCAGCTACTTGC[G/T]TGGCTGAGGCACAGG	9972
rs528655968	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654588	GCCTCCGAAAGTGCT[C/G]CGATTACAGGCATGA	9972
rs528722571	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702386	GTGGCAAGGCACCTG[C/T]AGTCCCAGCTACTCG	9972
rs528855514	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17642987	ATCCATAGAGACAGA[A/G]CACAAGTTGACAGTT	9972
rs528855568	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648999	ATGTATCCAAGATAT[C/T]TGTACATTTTTTTAA	9972
rs528959892	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17693976	TATAATAGGACACCC[A/G]TCTCATTTTGCTTCC	9972
rs529028197	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17649796	TGTGCCTACTTATAA[A/G]TTAAATTTCATCATA	9972
rs529037024	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695836	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	9972
rs529047552	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17646231	TTATTCCCCCGAGAC[A/G]GAGTCTTACTCTGTC	9972
rs529056601	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17623054	AGAATCACTTGAACC[C/T]GGGAAGCGGAGGTTG	9972
rs529065998	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674328	ATGTGTAATTTATAC[A/G]TCATTTAAAAAAAAG	9972
rs529074837	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682684	AGCACTTCGGGAGGC[C/T]GAGGGGTGCAGATCA	9972
rs529079267	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668136	GCTGGAGTGCAGTGG[C/T]GCGGCCTCGGCTCAC	9972
rs529095341	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630481	CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC	9972
rs529138639	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682039	ACAGTGAGGCCTCAC[A/G]TCTACTAAAAATTTT	9972
rs529146549	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668482	AAAAAAATTGGATGA[G/T]TATCTACTACATATA	9972
rs529148382	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661904	AAAATCTTAGATTTC[G/T]TTATATAAAGTTTCT	9972
rs529179305	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618108	CTCCATGCAGGAGAC[C/T]GGATGCATCTTCTTT	9972
rs529185943	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17695132	AAAACTTAAAATAGC[C/T]TTAAATCTCACAAAA	9972
rs529212424	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662615	TGAAAAGAATATAAT[G/T]GGGAAGTTTCCTTCC	9972
rs529231053	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677178	CTAAGGCCCACCACA[C/T]TGGGAGGCTTAGGAA	9972
rs529277693	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17700945	TTTTAAAAATAGCTA[A/G]GCAGTGGCTCATGCC	9972
rs529337310	snp	C/T	6.74343e-05	0.00580626	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706272	GCGGCGTCGGGGTCC[C/T]ATACCTGATGCTGTT	9972
rs529353984	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17667550	AACCCCATCTCTACT[-/A]AAAAATACAAAAAAT	9972
rs529405691	in-del	-/C	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705838	GATTCCAAGGGGCAG[-/C]CCCCCCTCCTCAAAC	9972
rs529441398	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17666069	GGCTCAAGCAATCCT[C/T]CTGCCTCAGCCTCTC	9972
rs529467013	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17689892	TCACTATTATTTTTA[C/T]TGTAGTTTGGCTATG	9972
rs529469616	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637986	TACAAAAGATGTTTT[C/G]TTTACAGGATATCAC	9972
rs529516251	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674845	AAAGTAATTTATTAT[C/T]CAGTTAAAGTGTAAA	9972
rs529528754	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17638918	TGAGAGAGCTGGACC[A/T]GAAAAATTGAATCCT	9972
rs529546278	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631265	CGCTGTGCAGGTGAT[G/T]GCTCACAATATAAAA	9972
rs529552990	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17681272	ATGACGAATACCAGT[A/G]GGCAACTCATGGAGA	9972
rs529561061	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669205	TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA	9972
rs529598226	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686903	GGGCGGCGGGGGAGG[A/G]GGGCGGGGAGTGGGG	9972
rs529609395	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17675836	TACCACAAATGGTTT[C/T]TACTTTAAGAAAACA	9972
rs529667600	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686800	AGTTGGGGGTAGGAA[C/G]GTAGGGAAATAGGCG	9972
rs529673781	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669668	ATTTAATGCATTAAC[A/G]GCAATTTATCTTTGG	9972
rs529694438	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625332	ATGAGGTCAGGAATT[C/T]GAGCCTGGCCAACAT	9972
rs529749302	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17693508	AGAAGGTAGTAGCGT[C/T]CTGCTATTGGTCTCT	9972
rs529780530	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17618862	TGAGCCACTGCGCCC[A/G]GCAGAAGTTAAAATC	9972
rs529811704	snp	G/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17699227	GCTAGCTGGGCGTGG[G/T]GGCTCAAGCCTGTAA	9972
rs529815892	snp	C/G/T	0.000342642	0.0130845	intron-variant	NUP153	GRCh38.p7	6:17651798	GGCCTCAAAATCCAT[C/G/T]AAACAAAAATTGAGG	9972
rs529842908	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17619400	CACCCAGGAAACGGG[C/T]TCCTCTACGAAGCTA	9972
rs529874028	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617928	TTAGTGTTTTAGTCT[C/T]TGTAGAAGTGTCTGG	9972
rs529922198	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17698793	AGAATCACTTGAATC[C/T]CAGAGCGGGGCGGAG	9972
rs529990088	snp	C/T	0.00206189	0.0320421	intron-variant	NUP153	GRCh38.p7	6:17629558	CAAAAATATAAAAGA[C/T]ACCACATAGACACTC	9972
rs529999119	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17646225	GCTTTTTTATTCCCC[C/T]GAGACGGAGTCTTAC	9972
rs530000451	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17704030	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9972
rs530031875	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676682	CTTTCAGACAGTGGA[A/G]AACAGCACAAAAAAA	9972
rs530051870	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17645275	AGAATTCTATGTTTT[A/T]ATTCTCTGATTATTC	9972
rs530141078	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640605	GATGAAATACTTATG[C/T]AGCCACAGAAATCAT	9972
rs530160860	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704890	TCAGCCTCCCAAGTA[A/G]CTGGGACTACAGGCG	9972
rs530162841	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677303	AAACAAGAACCAACA[C/T]TCTTCAGAGGAAGAT	9972
rs530164086	snp	A/C	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17679776	CTGAGGCTTTAGTCA[A/C]AAAAAGAAAACAGCC	9972
rs530176041	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708424	GCGCAATCTCAGCAA[C/T]CTCCACCTCCTGGGT	9972
rs530176120	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17665167	AATACAATGGTAGTT[A/C]TATTTTACATTATTT	9972
rs530201746	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17627579	CTGCTCACTGCCACC[G/T]CCGCCTCCCAGGTTC	9972
rs530211904	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671273	GTTGCTGTCTTCTAA[A/T]GTCTTTGTCTGATTT	9972
rs530232204	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17627544	TCTGTTGCCCAAGCT[A/G]GAGTGCACTGGGCCA	9972
rs530240001	in-del	-/AC	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17672584	CTGTCTCAAACAAAA[-/AC]ACAGAACAAAGACGG	9972
rs530267883	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660804	TATAATCCAACAATT[C/T]CATTCCTAGATAAAT	9972
rs530286219	in-del	-/CAAAAAAAA	0.0919752	0.193722	intron-variant	NUP153	GRCh38.p7	6:17678352	AGAACCCTCTGTCTC[-/CAAAAAAAA]AAAAAAAAAAAAAAA	9972
rs530290631	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685109	CTCAATTTGTAAAAA[A/T]TGCAGTATGTGCAAA	9972
rs530293359	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621218	ACAAAAATTAACAAC[C/T]GCTGGCAAGGAAATG	9972
rs530297021	snp	C/T	0.000104228	0.00721826	intron-variant	NUP153	GRCh38.p7	6:17665425	ACATTTATTTTCATA[C/T]AAATCAATGATTCAT	9972
rs530326444	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697780	GGGGAAGGCTATTCT[A/G]TAACACTAACTCAGA	9972
rs530360171	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659063	TTCTCTACAACAACA[C/T]CCAATGGCACACTGC	9972
rs530402847	in-del	-/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17633011	CTGTTCATATTTACA[-/T]TTGTTTAAAAAAAAG	9972
rs530423003	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659683	TCATCATGTTGGCCA[A/G]GATGGTCTCGATCTC	9972
rs530487086	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697121	GGCCCTAAAGCAAAG[C/T]CCACACTTCATAATC	9972
rs530489155	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653802	AATATTCAATCTCTT[A/G]ATAGGGCTTGCATTA	9972
rs530509555	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641288	TGCCTGTAATCCCAA[A/G]GACTTTGGGAGGCCA	9972
rs530511772	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648018	CTAAGTATTTTTTCC[C/T]TTTAAATTTAAAAAT	9972
rs530554973	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647436	ATTAAAGGACAGTCT[G/T]GGGATAATGGGGAAA	9972
rs530689296	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17641572	CAAACAAACAAAAAG[C/G]CCAGGCAGCGGTGGC	9972
rs530723493	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17683636	CACAGGCAGAGTAGA[C/T]TTAGCATAATTCTTA	9972
rs530784960	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683149	AACTTTCTCTAAACT[A/C]CTATTCATGTCAATA	9972
rs530796584	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17662617	AAAAGAATATAATTG[A/G]GAAGTTTCCTTCCCA	9972
rs530808398	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17665519	AGTAGATACAAACAA[A/G]TAAGAGGAAAAACTG	9972
rs530820670	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628528	TCCTTCCCAAAGAGT[C/T]CTGTATTTCTCAACT	9972
rs530847930	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666626	CCAAACCAAACCAAA[A/G]ATCTTACAATGTAAG	9972
rs530849244	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689494	CATTTCACTACAGCA[A/G]ATGTTGGCTGAAAAT	9972
rs530883030	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622137	TGGACAGTTATGCTG[C/T]TACCCAGAGTCAAGA	9972
rs530976660	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17655930	CAAGGTAGGGCTGGG[C/T]GCAGTGGTTCAACCC	9972
rs530985415	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17683162	CTCCTATTCATGTCA[A/C]TATTTGGACCTCCTC	9972
rs530991113	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616825	CACAATCTTGGCTCA[C/T]TGCAACCCTTGCCTC	9972
rs531033632	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695826	CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	9972
rs531036690	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17701598	CCCAGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGG	9972
rs531038732	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17649106	ATATAGGGTTTTTTT[A/T]AAATAAAGAATTAAG	9972
rs531148504	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707973	ATCTTTTTTTTTCTT[C/T]CTTTCTTTCTTTCTT	9972
rs531154459	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17701286	TATAATCCCAGCACT[C/T]TGAGAGGCCGAGGAG	9972
rs531285575	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636496	TTCATGAATAATGCA[C/T]TGAAAACAGTGTAAT	9972
rs531315608	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681890	ACTAAACCTAGTATA[C/T]ACAGAAACCAAAGAG	9972
rs531333472	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671750	GCTGGCTCATACCTA[C/T]AATACCAGCACTTTT	9972
rs531347999	snp	A/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630166	AAAGAAACTTTGAAA[A/G/T]ATTTACAAGAAACTA	9972
rs531355096	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624083	AGAAAATATAGGATT[A/T]TAATACAATTTGATT	9972
rs531380144	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682572	ATATTCTAAATTATT[A/C]TGTAATCTTAAAAAT	9972
rs531390081	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17688342	TAGGTAGTGTCTTCA[A/G]AATTAGGGCATGAAA	9972
rs531391514	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680631	TTTATGCATCAAAGA[A/G]TGTAATCAACAGAGT	9972
rs531410885	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17630545	GTCTGTGCCTGTAGT[A/C]TCAGCTGCTTGAGAG	9972
rs531443722	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17636929	TAAAACTGTACAAAA[A/C]GAGGAGGTCGTCATA	9972
rs531464753	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17701313	GGAGGCCAGACCACG[C/G]AGTGAGGAGTTCGAG	9972
rs531510524	snp	A/G	1.77404e-05	0.00297824	intron-variant	NUP153	GRCh38.p7	6:17669037	CAAGAGGCTGAAAAA[A/G]AAAAAAAACACTATT	9972
rs531518721	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656510	CTCCCTGGTAGCTGG[A/G]ACCACAGGCGCTAAC	9972
rs531548925	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17704118	TAACATGGTGAAACC[A/C]CGTCTCTACTAAAAA	9972
rs531570720	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687145	TACAGAGAATAAGAA[A/C]CTCTCCATGTCTTTC	9972
rs531572474	snp	A/C/T	0.0896555	0.191806	intron-variant	NUP153	GRCh38.p7	6:17663232	CTAAAAAGAAAAAAA[A/C/T]ACACACACACACACA	9972
rs531575056	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656763	AAAGGTTTAGGGGGT[A/G]GATTCTGGGGAAGGA	9972
rs531575502	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650900	CTACACAGCTGCAAT[A/C]TTGTTATTTTTACAG	9972
rs531602373	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17628089	ATGAAGTTCTTCCTG[C/T]TATTCAGCTCACAGA	9972
rs531607255	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618723	GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT	9972
rs531630381	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700870	CACTATCTGTGTCCC[G/T]TTCAGAAAAAGTTTA	9972
rs531631803	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694286	AGTTAGTATAGATTC[C/T]AAAATATTCACCAGG	9972
rs531633929	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705588	GGGTGGCGGTGTTGG[C/G]GGGGGGGAGGGGAGT	9972
rs531684754	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17638034	TTCTAGTTTGATGCT[C/T]TCAATGGTACTAATT	9972
rs531819941	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705137	GTGTAATCTTTATTA[A/G]CATCCAGAATAAAGT	9972
rs531820277	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645450	AGGCTCACACCACCA[C/T]CTGGTTATTTCTTTT	9972
rs531826883	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639756	AATTTCATTTTAGTA[C/T]AGAGTCCTTTGGCTT	9972
rs531861666	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669831	GGGCATGGTGGCTCA[C/T]GTCTGTAATCCCAGC	9972
rs531886026	snp	A/C	0.000123234	0.00784868	intron-variant	NUP153	GRCh38.p7	6:17688668	GAAATTTATCTTTTT[A/C]AAATAAGTACCTACT	9972
rs531886382	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17629626	GAAAGCCAAAGAAAC[A/G]TAGGAGTAACTTTGA	9972
rs531929354	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17675937	CTAGGCAAAACAAAG[C/T]TTCAACTAACTAAAA	9972
rs531930320	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625739	TGCTATATGATATTC[A/G]CTAAGAACTGACACA	9972
rs531951194	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693376	GAGAATGGGAGTAAA[A/G]AGAGGTCTTTTTTTG	9972
rs531993806	snp	C/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17676447	CTTTAGAATTTAATG[C/T]GTGTTGAAGTTACTC	9972
rs532018881	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658462	CAACAAAAAACAAAG[C/T]TTGCAAAGGAGACGA	9972
rs532048107	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665173	ATGGTAGTTATATTT[C/T]ACATTATTTAGTCTT	9972
rs532079140	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17658878	AAGCCAAACTTGCAC[A/G]CAAAAAAAGGCCATG	9972
rs532103408	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17698618	TGGTGGGCACCTGTA[C/G]TCCCAGCTACTTGGG	9972
rs532142245	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653055	CTCAGGAGTTTGAGA[A/C]CAGCCTGGGCAACAT	9972
rs532174271	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17646268	GCTGGAGTGCAGTGG[C/T]GCAATCCTGGCTCAC	9972
rs532216158	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17646333	CTGCCTCGGCCTCCC[A/G]AGCAGCTGGGACTAC	9972
rs532297077	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17647053	TGAGCCACCGTGCCC[A/G]GCCTCAAATGCCATT	9972
rs532297753	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17677380	AGTAAAAACTCAATG[C/T]ATAGAAAAAAGAAAA	9972
rs532356376	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641177	TGGGATTGTTGAAGA[C/G]TGACCTGACATGTAA	9972
rs532382289	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17679113	CATAATAAAGTAAAA[A/C]AACATGTTTGCAGAT	9972
rs532406400	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668718	CATGATGGCACGTGC[C/T]TGTAATCTCAGTTAC	9972
rs532419512	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17671375	AGAGTTTGTGTAGAA[C/T]TGGTATTATTTCTTT	9972
rs532427746	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640655	TGAGTGTCTTGTTGT[C/G]AGCAAGGCCGGAGTA	9972
rs532445008	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17685038	GACAGACATGTTAGC[A/G]TGTGCTGGTGGAAAA	9972
rs532502083	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17623482	CCATCAGGAAAAGTT[A/T]TTATTATCTTCTAGT	9972
rs532502989	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17632863	AAAAAAAAAAAAAAA[A/C]CGGGGAGTGGGGGGA	9972
rs532566325	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633799	CTCTTCCATAGTTAC[C/T]TAACTGATCTCTACA	9972
rs532582010	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17678425	AAGGAAGTAACAGTT[C/T]CTAAACTCCAAATAG	9972
rs532635345	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660385	AGCTAAGCTGAAATG[C/T]ATTTATAATACAACT	9972
rs532658086	in-del	-/A	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17672416	GACCCTGTCACTACC[-/A]AAAAAAAAATTTAGC	9972
rs532668790	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17616239	GCAAAATTTCCAAAT[A/G]CTAACATTTACCATG	9972
rs532685205	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702617	GGAGGCAGAGGTTGC[A/G]CTGAGCCGAGATTGC	9972
rs532695927	in-del	-/T	0.039522	0.134904	intron-variant	NUP153	GRCh38.p7	6:17668242	GCCACACCTGGCTAA[-/T]TTTTTTTTTGTATTT	9972
rs532705924	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17633770	TTCTCTAGATGGCCT[A/G]CAACTGTCGCCACCT	9972
rs532711547	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659750	TGCTGGGATTACAGG[A/C]ATGAGCCACCGTGCC	9972
rs532714852	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17694613	AGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG	9972
rs532748917	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615558	TCCTTAGCACGGACC[A/G]TTCTTTAATCAGGCT	9972
rs532787498	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17653882	TAACATTTCACTATA[C/T]GTCAATTTTGCTATG	9972
rs532851648	snp	C/T	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17696493	AGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGT	9972
rs532871924	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708262	TGGGATTACCCGTGT[A/G]AGCCGCCACGCCCAG	9972
rs532900659	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702430	GAAGAATGGCGTGAA[C/G]CCGGGAGGCAGAGCT	9972
rs532940562	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635405	TAAGCCACCGCACCC[A/G]GCCTATCATTATTTG	9972
rs533017085	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17698505	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	9972
rs533019210	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673097	CTTCTGGCTGGGCGC[A/G]GTGGCTCACGCCTGT	9972
rs533036900	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630009	GGCAGCTATAAACGA[A/C]GAAGGAAGAACAAAG	9972
rs533039122	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622521	GGTCTACCTTGTTAT[A/G]GAACTGAGAACCTCA	9972
rs533125538	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695762	CGCCTGTAATCCCAA[C/G]ACTTTAGGAGGCCAA	9972
rs533146327	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672930	ATTAAAACCTAAAAC[C/T]ATAAAACTTGTAGAA	9972
rs533152071	in-del	-/C	0.00557542	0.0525036	intron-variant	NUP153	GRCh38.p7	6:17689426	ACAAACAAAAAAAAA[-/C]AATCCAACAAAAATA	9972
rs533189705	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656070	TTTAGCTGGGCATGG[C/T]GGCGTACGCTTGTAA	9972
rs533195748	snp	A/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17683018	ATTGCAGTAATTCAG[A/T]CACATCTTCATACTC	9972
rs533201638	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17667437	AGAAAAATCCAAGCC[A/C]GGCACGGTGGCTCAC	9972
rs533304936	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701043	CCAGCCTGATCAACA[G/T]GGAGAAACCCCATCT	9972
rs533376379	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706455	CAGAGGCGGAGGCCT[C/T]AGAGAGCCTCCCCCG	9972
rs533381202	in-del	-/A	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707922	AAATGATTAGGGAGG[-/A]AAAATATGTTGTGAA	9972
rs533382188	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17644076	AGATAAGGTTGCAAA[C/T]ATACCAGTCAAATTC	9972
rs533406764	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17690379	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAGTATG	9972
rs533435654	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618078	GAACACTGGCAAATG[A/G]AGTTCTCTGATACCC	9972
rs533467424	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674419	AATAATGTTTATATA[C/T]CCTAAATGAAAAAAA	9972
rs533485334	snp	G/T	0.00993419	0.0697739	intron-variant	NUP153	GRCh38.p7	6:17692535	AAGACAAAAAGAAAG[G/T]AGGGAGGATGGGAAG	9972
rs533503418	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17668161	GCTCACTGCACCCTC[C/T]GCCTCCCGGGTTCAA	9972
rs533537454	snp	A/C/T	6.59287e-05	0.00574113	intron-variant	NUP153	GRCh38.p7	6:17662097	ATACACACATATTTA[A/C/T]GTTTGCTTATTTGTT	9972
rs533558889	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17686376	ATGTGCGCATGTCTT[A/C]ATTGTTAACAAACCT	9972
rs533596738	snp	A/C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656364	CACAAAATTGGCAGT[A/C/T]GGCCAGAATGAAGAG	9972
rs533798846	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696829	TGTAATCCCAGCACA[C/T]TGGGAGGCCGAGGTG	9972
rs533829773	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662833	AATCTAATCATGAGG[A/G]AACATCAGACAATCA	9972
rs533840816	snp	C/T	3.37729e-05	0.00410918	missense	NUP153	GRCh38.p7	6:17637755	GCAACAGAATCTATC[C/T]TCGGCGATGCGAAAC	9972
rs533853453	in-del	-/AC			intron-variant	NUP153	GRCh38.p7	6:17630342	AAAAACAGAAGAATT[-/AC]AGAGTTGAAGCAATG	9972
rs533881198	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673428	GGGAGAAAATATTCG[C/T]AAAACATATAACAAA	9972
rs533892514	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680900	AAAAGTAGAACCACA[A/G]TATGATCCAACAATC	9972
rs533950981	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17653558	TTCTTCCAGGTATTT[A/C]CCCCAGAGAAATAAA	9972
rs533954443	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686358	TTATGTAGGGCTAGG[C/T]TAATGTGCGCATGTC	9972
rs534009267	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17651058	TGTAATCCTAGCACT[C/T]TGGGAGGCCAAGGCA	9972
rs534013553	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703477	CCCAGAAACCCTTGG[A/G]CACTTAATCAAATAA	9972
rs534031732	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671306	GTCTCGGGGTAATAA[C/T]GTTGGCCTCATAAAA	9972
rs534060336	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643262	CAGATCACCTGAGGT[A/C]AGGAGTTCAAGACCA	9972
rs534068618	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625483	TGCAGTGAGCTGAGA[C/T]TGCACCACTGCACTC	9972
rs534087528	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17685524	ACTGCACTCCAGCCT[A/G]GGCAACAGAGCAAGA	9972
rs534135729	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692151	ATTAGGTATCTTCAA[A/T]AACAACTGGAAAACA	9972
rs534137357	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17698800	CTTGAATCCCAGAGC[A/G]GGGCGGAGGTTGCAG	9972
rs534180223	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17675156	AGACTCTTGTCTCAG[A/G]AAAAAAAAAAAAAAT	9972
rs534191098	in-del	-/CAAA	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17647265	GTGTTATTCTTACCC[-/CAAA]CATTCACTTTTCAAT	9972
rs534193966	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621276	TAAATTAGTATAACC[A/G]TTATGGAAAACAGTA	9972
rs534204361	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642196	TTCTTAGATATGACA[C/T]GAAAAGCACAGCAAC	9972
rs534219207	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631492	TTAATTAATTTCTCA[C/T]CATCTACCCCCCATC	9972
rs534233049	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651972	TGATGGCACATGCCT[A/G]TGGTCCCAGCTACTT	9972
rs534242557	snp	C/G	1.64849e-05	0.00287092	missense	NUP153	GRCh38.p7	6:17669439	ATTTACCGCTAAAGG[C/G]CTTGACATCTTCTCT	9972
rs534242811	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676034	ATACAACTATTTTTT[A/G]CCAGTTGATTAAACC	9972
rs534258116	in-del	-/TTTC	0.0414322	0.137839	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707967	CTATAAATCTTTTTT[-/TTTC]TTTCTTTCTTTCTTT	9972
rs534264866	snp	C/T	0.0111196	0.0737302	intron-variant	NUP153	GRCh38.p7	6:17656559	TTTGTTATTTTTTTG[C/T]ACACGTGGGGTTTTG	9972
rs534288915	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684660	TGCAAGAGGCCTAGC[C/T]TCAGGCCTGTCTCAG	9972
rs534294345	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645736	ACTACAACTATAATG[C/T]AGACAACCTATAAAT	9972
rs534298410	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17668407	TTTTATTTATCAAAA[C/G]GTAACAGTAAGCCAT	9972
rs534300122	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645518	GTGCTGCCTAGGATC[A/G]TCTTGAGCTTCTGGC	9972
rs534306891	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17669869	GAGGTGTGAGGAGGG[C/T]GGACTGCCTGAGCTC	9972
rs534352126	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17691289	ACACTAACTACTGAA[C/T]AACACCAATTCACTG	9972
rs534384830	snp	C/T	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17664150	TGAAGTACTGATACA[C/T]ACTACGACGTGAATG	9972
rs534427739	in-del	-/CT	0.0111196	0.0737302	intron-variant	NUP153	GRCh38.p7	6:17701217	GCAACAAGAGCGAAA[-/CT]CTGTCTAAAAAAAAA	9972
rs534435270	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679344	AAGATGTGCACATGG[A/C]AACTACAAAACAGTA	9972
rs534453284	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17666584	CGAATCCCTCTCCAA[C/G]TTATTTCCCCCATTG	9972
rs534465283	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17696552	CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	9972
rs534502362	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670626	CCTCATACCATTAAG[C/T]ATGTTGCCAGATGAT	9972
rs534521865	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702540	AATCAGCCGTTTGTG[A/G]TGGCGCATGCCTGTA	9972
rs534526099	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696099	TGCCATTGCACTCCA[A/G]CCTGGGTGACAAGAG	9972
rs534562326	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671062	GTGATCTAAGGCCTT[A/C]CAAAGTGCTGGGATT	9972
rs534585472	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702218	ACTAGAAAAATGACA[A/C]CATTTCTGGCCGGGC	9972
rs534623671	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665572	GTATTCATATACCTA[C/T]GCACATAAATATACA	9972
rs534641570	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683930	AAGTGGGGTCATGGG[A/G]AGTCTTTGGGTCATG	9972
rs534681788	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665859	CCGGCTAATTTTTTT[G/T]GTTTTTTTTTGTAGA	9972
rs534700279	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707351	TAGAAAATATATACG[A/G]CTTCATTAATGTTTC	9972
rs534708097	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690821	ACATTTCTGATACAG[A/G]CACTTGAATAGTAAT	9972
rs534714305	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640281	AACTTCCCCCACCAA[C/T]AAAAAGGCAAAAAAA	9972
rs534756270	in-del	-/T			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706952	TCGGCGCCCGACGCA[-/T]TTGCATCATCATGCT	9972
rs534769648	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17638732	GGGAGCAGGGGGAGG[G/T]TGGCATCATGAATGC	9972
rs534775407	snp	A/G	5.25776e-05	0.00512699	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632616	ACAAAAAGGCGCTTT[A/G]CCATCACCTTTATTT	9972
rs534794367	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683250	ATGTTCTTAATGTCA[C/T]CTAGAATGGTGAACC	9972
rs534827824	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672530	GCAGTGAGCCATGAT[C/T]GTGCCACTGCACTCC	9972
rs534834219	snp	C/T			intron-variant, synonymous-codon	NUP153	GRCh38.p7	6:17633529	GTAAGATGCTCATGG[C/T]CTTAAAGGGGGAAAA	9972
rs534854560	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682826	GGGAGACCGAGGCAG[A/G]AGAATTGCTTTATCG	9972
rs534944333	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17670387	GTATATTGACCTTGT[A/G]TCCTGTGACCCTGTT	9972
rs535019251	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621416	ACCTGATGTTTAGTG[C/T]AGCACTATTCACAAC	9972
rs535022547	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614695	ACCAAGAGACAACTG[C/T]AGTTTTTGTGTATGT	9972
rs535064594	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653420	AAAAGATGACTATCA[A/T]CTATTGGTAAGGATA	9972
rs535067637	snp	C/T	1.64746e-05	0.00287002	missense	NUP153	GRCh38.p7	6:17624705	CTGTGGAAGATGATA[C/T]AGATCCAAAGCCTGG	9972
rs535105830	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17701797	AAGATTGTGCCACTG[C/T]ACTCCAGCCTGGGCA	9972
rs535156738	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622252	CTCGGGAGTTAGAGA[A/C]CAGCCTGGATAACAT	9972
rs535202434	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647612	CAAATGGTACAGAAG[A/C]AAATGAATATGCATA	9972
rs535212004	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17616463	TGACTTTTAAAAACA[A/C]AACATATACATGCAC	9972
rs535269587	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641416	GGTACACACCTGTAG[C/T]CTCAGCTACTCAGGA	9972
rs535271460	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617058	CCGGCCGCAACATGA[C/T]AGGTTTTTAAATTAA	9972
rs535290097	in-del	-/AC	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17682022	AGACCAGCCTGGGCA[-/AC]ACAGTGAGGCCTCAC	9972
rs535316671	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17695459	GCTTAACTACAATAG[A/G]ATTTTACCTAAAAGA	9972
rs535332046	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655506	TCACCCAGGCAGGAG[C/T]GCAGTGGTACGATCT	9972
rs535335783	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641838	GGTTGGGAGACAGAG[C/T]GAGACTGTCTCAGAA	9972
rs535390224	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701616	CAGTGAGCCGAGGTC[A/G]CACCATTGCACTCCA	9972
rs535420275	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17688632	CCCTGTTGAGAGAAA[A/C]AACATATTATGACAG	9972
rs535492309	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643575	AATGAAAGTTAAATT[A/G]CTTTTAGTAATTTAC	9972
rs535494782	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17669131	TCGCCCAGGCTGGAG[C/T]GCAGTGGCGCGATCT	9972
rs535519073	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706689	AGATCTCCCGCAGAG[A/G]ACAGCACGAACAGTT	9972
rs535552990	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636729	ATCATTGCAACAGCT[A/G]CAGCCTTTTCATTAA	9972
rs535560212	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660841	GAGAAAATACTGCAC[A/G]TGTGCAGACAGAAAA	9972
rs535562173	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667481	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	9972
rs535564962	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17693822	ACCCAGGAGGCAGAG[G/T]TTGCAGTGAGCTGAG	9972
rs535582679	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706198	CTGCTCCACGTGGGG[A/C]GCCGGGGCCTCGAAC	9972
rs535587635	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707929	TAGGGAGGAAAAATA[C/T]GTTGTGAAAAATCTT	9972
rs535603313	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673957	TCAGTGTCTTTTCAC[C/T]GGTGAATAATAAACC	9972
rs535603724	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699396	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGCA	9972
rs535615724	snp	A/T	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17637512	GTTGTTTTGCCACTT[A/T]TATTTGGTGTTTCAA	9972
rs535625370	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661489	CCCATGAAATTTAAG[A/G]TACTAGATTAGGTTT	9972
rs535664642	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699018	ACACTAAGAAAAAGA[C/T]ATGCAAAATCAAGCA	9972
rs535670361	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705206	ATCAGATCCTTTTGC[C/T]ACACTTTTGTTTTTC	9972
rs535727958	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704540	AATCTTAAATCTGCT[A/C]GCAAATACCCCTTTT	9972
rs535749409	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681442	TACAAAAAATTAGCC[A/G]GGTGTGGTGGCGGGC	9972
rs535750175	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17656210	ACTCTGACAAATAAA[C/T]AAACAAACAAACCAC	9972
rs535764508	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662970	ACTAAAGGAGATGAA[A/G]AGACATGACAACTAA	9972
rs535804572	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687227	AGAAAAGATCATTTC[C/T]ACAGCTATCTTAGAA	9972
rs535807026	in-del	-/GCGACAGA			intron-variant	NUP153	GRCh38.p7	6:17653230	TGCACTCCAGCCTGG[-/GCGACAGA]GCGAGGCTCCATCTC	9972
rs535813180	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17681006	CAATAGCCAAGATAC[A/G]GAATTGACCTAAGTA	9972
rs535881031	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680038	CTGCATACCTTACCC[C/T]ATGTCAATTCCTGCG	9972
rs535918993	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17618745	TAATTTTTTGTATTT[-/C]TTAGTAGAGATGGGG	9972
rs535942698	snp	C/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706650	TGCGGACCCCCGCCT[C/G]TGTGTGTGTCACGGT	9972
rs535942856	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679511	TGCAGAAATAGAAAA[A/C]CCATCCTAAAATTCA	9972
rs536001212	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17680076	TAATAAAAAAAATTC[C/T]TACTGGCTTTTTCCG	9972
rs536005754	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17685418	GCTGGGCCTGGTGGC[A/G]GGCACCTGCAGTCCC	9972
rs536040764	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674486	TTAAATCAAAACTAC[C/T]GGCCGGGTGCAGTGG	9972
rs536057919	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17696421	AATAAGCAGGCATGA[C/G]GGAAATAAGCTTTCT	9972
rs536097387	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685867	AAAAAAAAAAATTGA[C/T]TCACAGGTGGTGGCT	9972
rs536124056	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17624325	TGAATGAATCCCATA[C/T]TTAAGTCAGAGTAAA	9972
rs536145088	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631578	AGCTACAACTTATAA[A/G]TAAGAAGATGAAATA	9972
rs536221112	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17635490	AACTGCAACCTCTAC[C/G]TCCCGAGCTCAAGCA	9972
rs536285911	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657408	TAAAAAAATAAAAAA[A/T]AAAAAAATAGCTAGC	9972
rs536302493	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678917	CACCACTGCACTCCA[A/G]CCTGACCAACAAAGC	9972
rs536302883	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17670409	GACCCTGTTAAACTC[A/G]CTTATTAGTTGTGGT	9972
rs536334136	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17619189	CCAGAAAAGTCTACA[A/G]TGGAGAAATGCTTTC	9972
rs536347692	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17651235	CTGAGTCCAGGAGTT[C/T]GAGGCTGTAGTGGGC	9972
rs536385780	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17657066	TAATTCTTTGGAGCA[C/T]GGCTTCACCTTCAGC	9972
rs536416791	snp	A/C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645089	GGCTCCGTCTCACAA[A/C/T]TAAAAGAAAAAAAAA	9972
rs536461971	snp	A/G	0.00279162	0.0372561	downstream-variant-500B	NUP153	GRCh38.p7	6:17614939	TGTCTAAATCATGTC[A/G]ATGTATTCTTCTAAT	9972
rs536536871	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691490	AGACTTAAGGCTGGG[C/T]GTGGTGGCTCATGCC	9972
rs536539219	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639349	CTCCCAAAGTGCTGG[C/G]ATTACAAGGGTGAGC	9972
rs536546257	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17653231	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGGCTC	9972
rs536598664	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631935	TCGGCCACTGCACTC[C/T]GGCCTGGGCGACAGA	9972
rs536600648	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17697544	ATGCAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC	9972
rs536605209	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690687	AGAGTCAAAGAAAGG[A/G]AAAAAATGACTCAGT	9972
rs536606942	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646616	TCTTATATTGAATGG[A/C]AATGTCACAGTTTAA	9972
rs536668683	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664088	ATATCTACAAAATCT[A/G]GTATTCCTTACAATG	9972
rs536670379	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17696528	TGAGAGGCCGAGGCG[A/G]GTGGATCACAAGGTC	9972
rs536675317	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640921	AGTCATCATGCCTGG[C/T]CCACAAAAATCATTC	9972
rs536738080	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633053	CTTTTAACCTTATAA[A/C]TGATTTCTTTTAACC	9972
rs536761005	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664758	CACTAACTTAAGATC[G/T]GACCAAGGTAGTGGC	9972
rs536800927	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620056	TGAGCCAAGATTGCA[C/T]CATTATACTCCAGCC	9972
rs536801458	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634068	TCAAATCTATTTCAA[C/T]CAATTTCTGACTCTT	9972
rs536822694	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658556	AGTTGACAAGGACCA[A/G]TTGAGAGCAATCATC	9972
rs536856683	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708278	AGCCGCCACGCCCAG[A/C]CTATTTACTATAAAT	9972
rs536868161	snp	A/C/G/T	0.00358938	0.0422398	intron-variant	NUP153	GRCh38.p7	6:17701706	AGGCGTGGTGGCCTG[A/C/G/T]GCCTGTAATCCCAGC	9972
rs536873770	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627964	CCCAAAACTTCTTAT[C/T]TTCTAGGCCACTCCT	9972
rs536888781	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17652814	GGATCACCTAAGGTC[A/C]GGAGTTCGAGACCAG	9972
rs536918280	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615489	GTGATAGGAGAATGA[A/T]AATATAGAAATAGCA	9972
rs536926581	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707633	ACATTAGGGGTAAGT[A/G]ATATATCCTTAACAA	9972
rs536933417	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621467	CTAAGTGTCCATCAA[C/T]AGATGGATACAGAAA	9972
rs536944504	snp	C/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17683898	ATCCTATGCTGAAAT[C/T]TGATCCTCAATGTTG	9972
rs536961966	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659910	TCAGATAATGATATA[C/T]AGTAATAGATTCCCT	9972
rs537067673	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689819	CATGAGCCACCGTGC[A/C]CAGCTATTATGGTAA	9972
rs537113117	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677595	GATTTTTAAGAAGAA[C/G]TGATAGCATTCCCAA	9972
rs537171178	in-del	-/A	0.000354123	0.0133017	intron-variant	NUP153	GRCh38.p7	6:17674867	AGTGTAAAAAAAAAG[-/A]AAAAAAAAAGATCAT	9972
rs537208475	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17688195	ATCAGAGCTTGCAGT[A/C]TTAACTGATATAGTT	9972
rs537215374	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642092	AAAATTCAAAATGGA[C/T]CAATATCCTAAATAT	9972
rs537329358	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694423	CAGCACTTCCGGAGG[C/T]CGACGCGGGCGGATT	9972
rs537369914	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17673137	ACTTTGGGAGGCCAA[C/T]GCGGGTGAATCACAA	9972
rs537392491	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700395	AGGCAGAACAGGGAT[C/T]CAAACTCAGGCTGAC	9972
rs537432264	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667567	AAAATACAAAAAATC[A/G]GCCAGGCATGGTGAT	9972
rs537433189	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17654113	GCACAGTTCTTTCAA[C/T]ATTTCATGTTTGAAA	9972
rs537444749	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17638452	AGAGAAGATGTAGAA[A/G]GTTATTAGAGGTTTT	9972
rs537496433	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647735	TCACCACCAGTGGCA[A/T]CTTAGATTTGATAAA	9972
rs537601868	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17660399	GCATTTATAATACAA[A/C]TAAAATGAGACTTGC	9972
rs537664136	snp	C/T	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17681457	GGGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	9972
rs537675736	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694854	CATGGTGGTGGGCAC[C/T]TGTAGACCCAGCTAC	9972
rs537712231	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17676022	ACAACAGTTGAAATA[A/C]AACTATTTTTTGCCA	9972
rs537735543	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17701126	GCTACTTGGGAGGCT[A/G]AAGCAGGAGAGTTGC	9972
rs537774811	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17679340	GTAAAAGATGTGCAC[A/G]TGGAAACTACAAAAC	9972
rs537786863	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706607	GTGGCGGCCGCAGAG[A/G]CCGAGGAGGCTCCGG	9972
rs537793382	snp	C/T	1.65737e-05	0.00287864	missense	NUP153	GRCh38.p7	6:17629483	AGGATGATGAGACAC[C/T]AAATTTGAAGGATGA	9972
rs537816656	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636827	GGAGAAGTAATATTT[C/T]ACTCTGTACAAAGGT	9972
rs537847601	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706159	CCCGGAGCCTCACTC[A/G]GGCCTTTCCTCAGGC	9972
rs537877030	snp	A/G	1.65419e-05	0.00287588	missense	NUP153	GRCh38.p7	6:17637716	CTTGTATAAACTACT[A/G]GGCTTGTTGCGGTGG	9972
rs537897067	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668163	TCACTGCACCCTCCG[C/T]CTCCCGGGTTCAAGT	9972
rs537909381	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17652376	TTAGAAATCAATACC[C/T]TCCCCCCCAAATATT	9972
rs537940449	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17630775	GAGGGGAGAGGGGAG[A/G]GGAGAGAAGAGAGAA	9972
rs537940882	snp	G/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17698958	TCACACTTTTTCTCA[G/T]GTAACATGTTTGAAA	9972
rs537953887	snp	A/G	0.000247494	0.0111214	intron-variant	NUP153	GRCh38.p7	6:17661976	ATACAGACCTTACAA[A/G]TTAAATATAAAGAAG	9972
rs537979560	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668811	TGGCACCACTGCACA[C/T]CAGTCTGGATGACAG	9972
rs537985143	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697340	TCAGGAACATTCAAC[A/G]TATAAGGTATTGTGA	9972
rs537992889	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617694	TAAAAAATTTTTCAA[A/C]ATTAGCCAGGCGTAG	9972
rs537999495	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704393	TATATTTAAAACAAG[C/T]CATTTTTCTACATGT	9972
rs538007943	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648501	GCGCACCTGTAATCC[C/T]AGCTACTCAGGAGGC	9972
rs538012168	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624357	ATTAACACTTTAAAA[A/T]ACATTACTACCTTAA	9972
rs538191286	in-del	-/GGGAGGGGAGAA			intron-variant	NUP153	GRCh38.p7	6:17630739	GACAAGAGGGGAGAG[-/GGGAGGGGAGAA]GGGAGGGGAGAGGGG	9972
rs538203406	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686087	TGGAAGGTTGAGGTT[A/G]CAGTGAGCCATGATG	9972
rs538227366	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679406	TCCCACGTACATGGA[C/G]TACAAGACTAAATAT	9972
rs538260388	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673836	ACTTACCATATGACC[C/T]ATCAATTCAACTCCT	9972
rs538288053	snp	C/T	0.000399281	0.0141238	missense, intron-variant	NUP153	GRCh38.p7	6:17651875	AAGATGGGATGATCG[C/T]TTGAGCGCAGGAGCT	9972
rs538303688	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674549	CGGGGTGGGCGCATC[A/G]CGAGGTCAAGAGATC	9972
rs538321191	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618605	GAGTCTGGCTCTGTT[A/G]CCCAGGCTGGAGTGC	9972
rs538343194	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17691910	TCAAACTCCTGGGCT[C/G]TCATCTCAGCCTTCC	9972
rs538382536	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699693	ATACAAAAATAGCCA[A/G]GCGTGGTGGCACACA	9972
rs538382676	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17652398	CCAAATATTAGGAAA[G/T]TCAATACATTTCTAA	9972
rs538441497	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703625	ACCAAAGCCTCAATA[A/G]GGACTAAAGAAAGTC	9972
rs538475048	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697468	AGGCAGACAGGTCAC[C/G]TGAGGTCAGGAGTTC	9972
rs538479963	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17663605	TAATGTTAACTTAAA[A/G]GTATGGAGGGAGATA	9972
rs538506142	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676744	CTCTCTGTCTAGGAA[C/T]ATTTTCAGACCTTGA	9972
rs538517576	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670013	GGCAGGAGAACTGCT[C/T]TGAACCCAGGAGGCG	9972
rs538526710	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17696583	ACACGGTGAAACCCC[A/G]TCTCTATTAAAAATA	9972
rs538603103	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635226	ACCATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	9972
rs538705748	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665523	GATACAAACAAATAA[C/G]AGGAAAAACTGATAA	9972
rs538714090	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699590	GCCTGTAATCCCAGC[A/G]CTTTGGGAAGCCGAG	9972
rs538731034	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645672	CCTGCATAACCTTTA[C/T]ACATAAAAATGCTTG	9972
rs538754923	snp	A/C			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632320	AAACAAACAAACAAA[A/C]AAAAAAACAAACAAA	9972
rs538794390	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639467	ATCTGAGAACTATTT[A/C]TCCCCTTTCTAATTA	9972
rs538867699	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631973	ACCATCTCAAAAAAA[A/C]CACAAAAATCTGGCC	9972
rs538927725	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632435	ATTTTTTTTCCCACC[G/T]GGAGAAAAGATACCT	9972
rs538946554	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670544	GATTTCTGTGCCTAC[C/T]GCACTGGCTAGCACC	9972
rs538973227	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702584	GGGAGGCTGAGGCAG[A/G]AGAATAGCTTGAACC	9972
rs539003281	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633088	AAATGAGCAGCTCAT[A/C]ATCACCTTGCTCACT	9972
rs539010146	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664801	CTCACATCTGTAATC[C/T]CAGCACTTTGGGAGG	9972
rs539140345	snp	A/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17628037	ACTGGTGCACTAAGT[A/T]TGGGGAAATTCTAGT	9972
rs539143699	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652911	GCGCACACCTGTAAT[C/T]CCAGCTACTAGGGAG	9972
rs539204106	snp	A/T	0.0110949	0.0736503	intron-variant	NUP153	GRCh38.p7	6:17628625	TAAAAAAAAAAATAA[A/T]AATAATAATAATAAA	9972
rs539207070	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653362	ATGCAAATTAAAATT[A/G]CAATGAGATACCACC	9972
rs539267947	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706859	CGTCGTCGTCGTCCC[C/T]GCAGCCTCCGCCGCC	9972
rs539269452	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17622239	TGGACTGCTTGAGCT[C/T]GGGAGTTAGAGACCA	9972
rs539303607	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660673	TGTCCAAAAAACACA[C/T]AAAAGGATGCCCCAA	9972
rs539314326	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641051	CTTTTACTTTTTATG[A/C]TTTCTAAACTTGCAT	9972
rs539334637	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689738	CCATGTTGGTCAGGC[C/T]GGCCTCAAACTCCCG	9972
rs539390500	snp	A/C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704443	ACTCAAAGGCATTCA[A/C/T]AGGAGAAAAGAAAGC	9972
rs539399261	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695935	AATGGCGTGAACCCG[A/G]AAGGCGGAGCTTGCA	9972
rs539400999	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643024	GGGGAAGGCAGAATG[A/G]GGAGCAACTTTTTAA	9972
rs539478072	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17650898	AACTACACAGCTGCA[A/G]TCTTGTTATTTTTAC	9972
rs539480414	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681492	TGGGAGGCTGAGACA[G/T]GAGAGTGGCGTGAAC	9972
rs539480875	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17648645	ATATTTAAAAAAAAA[A/T]TTTTTTAATTAGCTG	9972
rs539537469	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694721	CGGTGGCTTACTCCT[A/G]TAAGCCCAGCGCTTT	9972
rs539543060	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687326	GGGGGGAAAACAGAA[A/T]AAGAAAAGCCAGAGT	9972
rs539561418	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672233	ATCAATGGGTGGGTC[A/G]GGGGAGGGATGGTCA	9972
rs539599020	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694417	TAATCCCAGCACTTC[C/T]GGAGGCCGACGCGGG	9972
rs539603487	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635713	CTATTGCCTATATGA[C/T]TGATACCACTTCCTA	9972
rs539640373	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615820	CAGGCTCCATTCCTG[A/G]GTACAGCCAGACTAT	9972
rs539650544	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658837	GCTCAGTGGTTAACC[A/G]AGAAGTAGCTTCAAA	9972
rs539665200	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693928	TCTAGTAGAAATTTG[A/C]ATGGCCTCTTTACTT	9972
rs539670017	in-del	-/T	0.0640965	0.167152	intron-variant	NUP153	GRCh38.p7	6:17645303	TCATTCATTTCTTTC[-/T]TTTTTTTTTGAGATA	9972
rs539732816	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661390	AAACAGACAAAACTA[C/T]ACAGTAATACCAAGG	9972
rs539738232	in-del	-/T	0.325799	0.238232	intron-variant	NUP153	GRCh38.p7	6:17691822	GCACTATAGCAAGAA[-/T]TTTTTTTTTTTCCAG	9972
rs539759637	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17646356	GGGACTACAGGAACT[C/T]GCCACCACACCCGGC	9972
rs539765181	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668213	CCGGAGTAGCTGAGA[C/T]TACAGGTGCGCACCG	9972
rs539765528	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616996	ACCTTGTGATCTGTC[C/T]ACCTCGGCCTCCCAA	9972
rs539776417	snp	A/G	5.03157e-05	0.00501551	intron-variant	NUP153	GRCh38.p7	6:17669269	TGAACAATATTTTGT[A/G]AAAAGGTTTAAATCT	9972
rs539849874	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698554	CCATCCCGGCTAACA[C/T]GGTGAAACCCCATCT	9972
rs539915492	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17623077	GGAGGTTGCAGTGAG[C/T]GGAGATCAAGCCACT	9972
rs539963966	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643322	ACTAAAAATACAAAA[A/T]TTAGCCAGGCATGGT	9972
rs540025006	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636210	TGTGGTGGCATGCAC[A/C]TGTAATTCCAGCTAC	9972
rs540067243	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679590	ACAAAAAAGTTGGAG[G/T]TCTCAAGCTTTCTGA	9972
rs540072566	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17630036	AAAGATGTGTCCAAG[A/G]TAATCCCTGATAAAA	9972
rs540094524	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17678961	TTAAAAAAAAAAAAA[A/T]AATAAGTCTTAACAA	9972
rs540110667	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706071	GAAAGGCGGCCCAAA[C/T]CACACGTGTGCGCCG	9972
rs540129547	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678968	AAAAAAAAAAATAAG[G/T]CTTAACAAATATTTT	9972
rs540133587	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17630443	GGCGGGCAGATCACC[A/C]GAGGTCAGGAGTTCA	9972
rs540187794	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17623963	GGGCTTCCAGGTGGT[C/T]GTTATACAGCATTTG	9972
rs540216016	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17655665	CACCATGTTGGCCAG[A/G]CTGGTCTCGAGCTCC	9972
rs540219759	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648553	ACCCGGGAGGTGGAG[G/T]TTGCAGTGAGCCAAG	9972
rs540221636	snp	C/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630950	ATCATTAAGAAGTAC[C/G/T]AAGATACTTAAAAGT	9972
rs540227928	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17653300	AAGATACACAAATGG[A/C]CAATGAGCACATAAA	9972
rs540234307	snp	C/T	0.0217236	0.101931	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704748	AAAAAAAAAAATTCC[C/T]CAAATCTTTACTTTT	9972
rs540278960	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648958	CTCTATGGTATTGCA[C/T]AAGAGTTGAGGAACA	9972
rs540282445	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17618083	CTGGCAAATGAAGTT[C/T]TCTGATACCCTCCAT	9972
rs540400102	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17692517	CCTGTTTCTAAAAAC[-/AA]AAAGACAAAAAGAAA	9972
rs540411228	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650649	AAACAAAGAATCTAC[C/T]TCTATAAAACCTGCT	9972
rs540446741	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17621029	CAAAACAAAAACAAC[C/T]AAATAATCCCACTGA	9972
rs540472913	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651580	CATGGACAGGCTCAA[A/C]GTATATGAATGGAAA	9972
rs540627111	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668859	AAAAAAAAAAGAATA[C/T]TATTTTTCAAACATG	9972
rs540646916	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17646218	ATATAGAGCTTTTTT[A/C]TTCCCCCGAGACGGA	9972
rs540680299	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664429	AGGGTGAGGGTTTGA[A/G]GTCTGGAAAAACAAA	9972
rs540704102	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639590	TGTTCCATATTTACC[A/C]AACTGGGGAATAATT	9972
rs540710281	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697688	GCGAGACTCCATCTC[A/T]AAAAAAAGGATTAAT	9972
rs540737503	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676275	CTGTTTATAACCTAA[A/G]GTAATCTCTTAAATA	9972
rs540743001	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656968	GTCAGTTTTGTTATC[C/T]TGCAAGTGGAGAGGG	9972
rs540768110	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632032	AGGGAGTCTTCCTTT[A/G]TACTTATATAGTAAA	9972
rs540811400	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617777	CTGAGCCTAGGAGGT[C/T]GAGGACGCAGTGTGC	9972
rs540817985	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17664424	TGGCCAGGGTGAGGG[C/T]TTGAGGTCTGGAAAA	9972
rs540838994	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702601	GAATAGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	9972
rs540840386	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661910	TTAGATTTCTTTATA[C/T]AAAGTTTCTGTTCTT	9972
rs540881234	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664978	GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC	9972
rs540900004	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17702398	CTGTAGTCCCAGCTA[A/C]TCGGGAGGCTGAGGC	9972
rs540969098	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695135	ACTTAAAATAGCTTT[A/G]AATCTCACAAAATTC	9972
rs540983096	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658713	TGAGTGAAAATTTAA[A/G]AAATTGTTTTGAAGT	9972
rs541002753	snp	C/T	0.0170251	0.090679	intron-variant	NUP153	GRCh38.p7	6:17618808	CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	9972
rs541057899	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17631700	GACCAGGCGTGTTGG[C/T]TCACGCCTGTAATCC	9972
rs541068682	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707783	ACATAGTCCAACCCT[C/G]TCATTCAACCAACCA	9972
rs541068755	snp	C/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708018	AGAGTCTTGCCCTGT[C/G]GCCCAGGCTGGAGTG	9972
rs541161236	in-del	-/T	0.0119091	0.0762411	intron-variant	NUP153	GRCh38.p7	6:17634979	AAACAAATTAAAAAA[-/T]AAAAAAAAAAAATAA	9972
rs541180045	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625648	CACAGAGAGTGTACA[C/T]TATTCCATACAGTGA	9972
rs541243450	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17619336	ACCCTCAAGAATCAC[C/T]GGAAGATGTGCTGTA	9972
rs541268649	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677933	TTGTGTCAATTGCTA[C/G]AGTTTTCTTATTCTA	9972
rs541301014	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633322	TCAAGATTTGAAAGC[A/G]TAGATCTCTGCCTCT	9972
rs541316970	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681648	CTGCTGGTATAGGTA[C/T]TTAAACCAATTAGCA	9972
rs541329586	snp	A/G			synonymous-codon	NUP153	GRCh38.p7	6:17616547	TGTAAATGCTGCTGG[A/G]GACTGGTTAAATGGA	9972
rs541376062	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621131	TGCTCAACATCACTA[C/T]CATAAGGGAAATGCA	9972
rs541394447	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17677917	TTTTTCAATATTAAC[-/TT]TGTGTCAATTGCTAG	9972
rs541395832	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668144	GCAGTGGCGCGGCCT[C/T]GGCTCACTGCACCCT	9972
rs541437345	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17621700	CAGAGGCTTCGTTGG[A/G]GTGGTGGTAGGAAGG	9972
rs541439267	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614988	ATTTTACAAAGTCCC[C/T]CCAATAATACTGTGT	9972
rs541440958	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17665154	ATACAGTTGCTAGAA[C/T]ACAATGGTAGTTATA	9972
rs541457182	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17682735	CATCCTTGCCAACAC[A/G]GTGAAACCCCATCTC	9972
rs541477397	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17646389	ATTTTTTGTATTTTA[A/G]TAGAGATGGGGTTTC	9972
rs541500892	in-del	-/AT			intron-variant	NUP153	GRCh38.p7	6:17660568	TATACATATACATAC[-/AT]ATTTCTTAATATACA	9972
rs541502491	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615954	TGGGGCTTCTGTAAC[A/G]AAAGAGAAAGGAGGA	9972
rs541515975	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660285	TACTCCTAAAACTCA[C/T]TGGTCAATGAGGGAG	9972
rs541555512	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17677216	GGACTTGTCCCCACA[A/G]ATATACATTAATACA	9972
rs541576799	snp	A/G	0.000399281	0.0141238	synonymous-codon, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632819	GACAGGTACAGTGCT[A/G]CTACTTGAAGCAGGT	9972
rs541586377	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17689294	CAGGAGGCTGAGGCA[A/G]GAGAATCACTTATAT	9972
rs541612464	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641108	AGTGTGATAATGGTT[A/T]TATCGTTATATTTTT	9972
rs541647523	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644116	GCCACTTCCATAATC[C/T]GGCCTCTTATCTTCA	9972
rs541668705	in-del	-/C	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17677169	GCTTGGAGGCTAAGG[-/C]CCACCACATTGGGAG	9972
rs541700944	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17657518	GCCATGAGCCAAGAT[C/T]GTGCACTCCAGCCTG	9972
rs541758344	snp	A/G	4.94385e-05	0.0049716	synonymous-codon	NUP153	GRCh38.p7	6:17662044	TTCTCTATTTTGTCC[A/G]GGTGTCATATTTTTT	9972
rs541802655	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659622	GGACTACACACATAC[A/G]CTATCACACCCAGCT	9972
rs541821691	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635286	GGCTAATTTTTTGTA[C/T]TGTTAGTAGAGACAG	9972
rs541827057	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694430	TCCGGAGGCCGACGC[A/G]GGCGGATTACCTGAG	9972
rs541860572	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672663	ACTAGAACAATTGCA[A/C]ACCCATATGTTAAAA	9972
rs541883052	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17644948	AAAATTAGCCAGGCG[C/T]GGTGGCAGGCGCCTG	9972
rs541883405	snp	A/G	0.000399281	0.0141238	synonymous-codon	NUP153	GRCh38.p7	6:17629097	TATGGTGTTAGCAGG[A/G]GCAGGGGTGGAGTTA	9972
rs541885795	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17667289	ATAAAAAGTTCAATA[C/T]TAGCTTTCTTTGCAT	9972
rs541947103	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667703	CCTGGGTGACAGAGC[A/G]AGACGCTGCCTCAAA	9972
rs541986664	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654913	GGCAGAAATCTTACA[C/G]ACATGAACACAATAT	9972
rs542046452	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705409	ACATCCAGGAGTTCA[C/T]ACAGTGGCTAAACTA	9972
rs542071405	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17692275	AACTAGTCTCAGCCC[A/G]GAAGAGCTTAATAGA	9972
rs542108164	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655879	AAACAACTATATAAT[C/T]GTGTATCCAAACCTA	9972
rs542216434	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17703096	CCAACTACTTGGGAG[A/G]CTGAGGCAAGAGAAT	9972
rs542228411	in-del	-/A	0.00199481	0.0315187	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615351	GACTAAACAAACAAC[-/A]AAAAAAATCTCTAAC	9972
rs542260336	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631654	TTGCGGGCTTACTCT[C/T]TTACAGAAGACTTGA	9972
rs542270641	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680244	CTGTGGTCTGTAATA[C/T]TGTAATAAAGACAGG	9972
rs542273763	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673268	CAGCTACTCAGGAGG[C/G]TGACGCAGAGAATTG	9972
rs542296355	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17629768	ACTTTTCATTTATCA[C/G]ACTGGCTGCGATAAA	9972
rs542300086	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17686204	TGTAAACAGCCTTAG[C/G]TAAGTCCTTCTGGAA	9972
rs542329631	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666399	ATGCGCCTGTAATCC[C/T]GGCTATTCAGGAGGC	9972
rs542342363	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622405	AGCAGGTTGAGGCAG[C/T]AGTGAGCCGAGATTC	9972
rs542359761	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693029	TCTTACAGACCATTT[C/T]AGACTGTGCTAAATA	9972
rs542377317	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678763	AGCCTGGGCAACATA[A/C]TGAGACTTCATCTCT	9972
rs542396782	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674334	AATTTATACGTCATT[A/T]AAAAAAAAGAATCAC	9972
rs542403605	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622866	CTGGGCGTGGTGGCT[A/C]ACACCTGTAATCCCA	9972
rs542420597	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700960	AGCAGTGGCTCATGC[C/T]TGTAATCCCAGCACT	9972
rs542423222	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630496	GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAA	9972
rs542465002	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617402	AAGCAATTGCATTTA[C/T]ACCAAACATACCCAA	9972
rs542501983	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684299	TAACTTATTGCAGCT[C/G]CTACATCAGCACTTG	9972
rs542517751	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617856	TCTCAGAAGGAAAAG[A/G]AAAAAAAAGAAAAAA	9972
rs542547710	in-del	-/A	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17683134	ATGGGGGCTGGAATC[-/A]ACTTTCTCTAAACTC	9972
rs542553583	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697807	CAGAAACAGCTGGGG[A/T]GGGGGAAGGCTATTC	9972
rs542582947	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649821	ATCATAGATATGTAT[A/G]TATAAGAAAAAACAC	9972
rs542616279	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625172	ATGTGCATATATACA[C/T]TGCATAATAAAGACT	9972
rs542637325	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17618802	CGATATCCTGACCTC[A/G]TGATCTGCCCGCCTT	9972
rs542667723	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17636758	AACGACTATAGTCTA[C/T]CCCCTAAAGAAACCT	9972
rs542669212	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17696647	GTAGTCCCAGCTCCT[C/T]GGGAGGCTGAGGCAG	9972
rs542683807	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643921	TCATAATAAGTCATG[A/C]AATTGGTAATTTGAA	9972
rs542744111	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682240	AACAACATACCTACT[C/T]AAAAAAAAATTGCTA	9972
rs542745073	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644523	TTTTTCTCTTGTTCC[C/T]GTGCCCTTGAGCTTT	9972
rs542807889	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17674721	GTTGCAGTGTGGTCC[A/G]AGATTGTGCCACCGC	9972
rs542827431	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654358	CGGAGTTTCGATCTT[A/G]TTGCCCGGGCCGGAC	9972
rs542870868	snp	C/T	0.000813296	0.0201491	missense, intron-variant	NUP153	GRCh38.p7	6:17668985	TTTACCTTTTCTCTT[C/T]TGGCCTGAAAATCTG	9972
rs542895814	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645967	CTAATTTCATCCAAA[G/T]GAAGGCATTTATAAG	9972
rs542905767	snp	C/G	3.29685e-05	0.00405995	synonymous-codon	NUP153	GRCh38.p7	6:17624583	AGGAGTTGTTCCAGA[C/G]CCAAATGCAGACTGA	9972
rs542917720	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17639691	ATTCCTCACTGACCT[A/G]CCTCTATTAATGGAG	9972
rs542939047	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17697843	ACTAACTCAGAACTC[-/A]ACTTGTAATTAACGA	9972
rs542968300	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663182	GTGAAGTTCATGAAA[A/T]TTTTCTTGCAAATCT	9972
rs542977911	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17674544	GAGGCCGGGGTGGGC[A/G]CATCACGAGGTCAAG	9972
rs542979007	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632111	AGCCTGTATCGCTTT[C/T]AATTTAGAGGTGTAT	9972
rs543031514	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663742	TGTTAGAAATGAGAT[A/T]AAATATAACTAAAGG	9972
rs543031683	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17657138	GCTCAGGTTGATTAT[C/T]TATAGCTTAGTTTTG	9972
rs543051447	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676967	GATACTAGACAGTGT[A/C]CCGTGCTAGGGGAAA	9972
rs543078844	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664467	GCAGTATCTGAACCT[C/T]GCTCGAGTCCTGGTT	9972
rs543083479	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696319	GAAGAAAAGGTTCCT[C/T]TGACCTTACTACCAA	9972
rs543114748	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670737	GTTGGATTTTTAAAA[A/T]ATATTTTATGTATCT	9972
rs543123137	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702591	TGAGGCAGGAGAATA[C/G]CTTGAACCCAGGAGG	9972
rs543126380	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17651627	CTACTAAGCATAAGA[A/G]GGCTTATTCCAGTAA	9972
rs543141602	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665163	CTAGAATACAATGGT[A/G]GTTATATTTTACATT	9972
rs543148537	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659174	CTGACTATCACTTCT[C/T]CAAGCATCTCGAAAA	9972
rs543181795	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17702372	ATTAGCCGGACGTGG[C/T]GGCAAGGCACCTGTA	9972
rs543183105	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707425	TTCTGGTTCTGCCAC[C/T]CAACCTATTTGACCT	9972
rs543183227	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17680755	AGTGAAAATGGCTTT[C/T]ATCAAAAAGGCAATA	9972
rs543186237	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638711	TTCCTATTTAAGAAG[C/T]AAAAAGGGAGCAGGG	9972
rs543219965	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682625	GTAGATTCCATCTCA[C/T]GAAACCACTTTTGCC	9972
rs543249282	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708591	AGGTGATCTGCCCAC[A/G]GCCTCCCAAAGTGCT	9972
rs543354408	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706899	ATTACCCCTGCTAAG[A/G]CGGCTGCCGCGGTCG	9972
rs543406654	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670205	GTAATAACAGAATAC[C/T]GTCCTCCACCAACAC	9972
rs543427175	in-del	-/TTTT	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17622099	GTAGCATGGCTTTTC[-/TTTT]GTTTTGTTTTGTGTT	9972
rs543433491	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647047	CAGGCATGAGCCACC[A/G]TGCCCGGCCTCAAAT	9972
rs543467478	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17682931	AAAAAAGAAGAAAAA[A/G]AAAAAAAAAAACACT	9972
rs543468755	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17636021	GGGGAACCAGATGGG[A/C]AGACAAAAATATTTC	9972
rs543485183	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678104	TTCACACCTGTAATC[C/G]CAGCACTTTGGGAGG	9972
rs543502148	snp	C/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619402	CCCAGGAAACGGGTT[C/G/T]CTCTACGAAGCTAAA	9972
rs543571185	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681606	ACAAAAATAAAAAAC[C/T]AGAGATACTGTCTGG	9972
rs543593216	snp	A/G	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17688501	TATTTTCTGGCCAGC[A/G]TGGAACCTCGCTTGT	9972
rs543632151	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681225	TTAAAAAAAAAAAAC[A/G]GACTCAAAAGAACTC	9972
rs543633926	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687689	ATTTATTTGAGACTT[C/T]AACATAGGGCTACAA	9972
rs543652385	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17675156	GACTCTTGTCTCAGA[-/A]AAAAAAAAAAAAAAT	9972
rs543655145	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653019	AGCATTTGGTAGGCC[A/G]AGGCGGGTGGACTGC	9972
rs543715919	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17646413	GGGTTTCACTGTGTT[A/C]GCCAGGATGGTCTCG	9972
rs543719260	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666334	CCAGCCTGGCCAACA[C/T]GGTGAAAACGTCTCT	9972
rs543728384	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614759	ACTTACCAAGGAAGA[C/T]AGAAGCACAAAGAGA	9972
rs543755411	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621801	GAGTTAACAATAATT[A/T]ATTGTACATTTCAAA	9972
rs543755703	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676593	GGCTTCCAGTTAGAA[C/T]GGAATAAGTGGGACC	9972
rs543793693	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17656030	GCCAACATGGTGAAA[C/T]CCCATCTCTACTAAC	9972
rs543812431	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618091	TGAAGTTCTCTGATA[C/T]CCTCCATGCAGGAGA	9972
rs543949808	snp	C/T	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17699198	CAAATAATTTTTTTT[C/T]TTTTTAAATACAAGC	9972
rs543998618	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17634697	CTGCCTCAGCCTCAC[A/G]AAGTGCTGGGATTAC	9972
rs544056867	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642734	ACAAATACACATACA[C/T]ATATGTTCACAGCAG	9972
rs544205557	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699664	AACATGGTGAAACCC[C/T]GTGTCTACTAAAAAT	9972
rs544212308	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654477	CAGGCACCTGCCACT[A/G]CGCCCAGCTAATTTT	9972
rs544215609	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673426	ATGGGAGAAAATATT[C/T]GCAAAACATATAACA	9972
rs544229138	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630385	AAACATCAGACTGGG[C/T]GTGGTAGCTCACGCT	9972
rs544296607	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705313	ATTCAATACTTCTAA[C/T]AATCAATATTTTAAA	9972
rs544363301	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704954	GTTAGTAGGGACGGG[G/T]TTTCACCGTCTCTGG	9972
rs544435872	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643255	AGGCGGCCAGATCAC[C/T]TGAGGTCAGGAGTTC	9972
rs544490157	snp	A/C	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17697769	CAGCTGGGGTGGGGG[A/C]AGGCTATTCTATAAC	9972
rs544638777	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17685635	TCCCTAGTGACATCA[C/T]AGCCATCCTAAGGCC	9972
rs544675740	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17674750	GCACTCCAGCCTGGG[C/T]GACAGAGCCAAGACT	9972
rs544705773	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685040	CAGACATGTTAGCGT[A/G]TGCTGGTGGAAAAAT	9972
rs544715537	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662340	TAACCTAACCACAAA[A/G]TTACTTTACTTATCC	9972
rs544739076	snp	A/G	0.000297025	0.0121829	synonymous-codon	NUP153	GRCh38.p7	6:17675547	AGCTCTTGAAGAAAA[A/G]CCACTGGTAGTTGAG	9972
rs544764123	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691617	TAAAAATACAAAAAT[G/T]AGCCAGGCATGATGG	9972
rs544767905	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17700980	ATCCCAGCACTTCGC[A/G]GGAGGCCAAGGCAGG	9972
rs544806829	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654164	GAGGAGGAACAAACA[A/G]AAGATGCATCTGGCT	9972
rs544809738	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669095	CCTTTTTTTTTTTTT[C/T]TGAGATGGAGTCTCA	9972
rs544834963	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684140	GCCAAGCAGATGCTG[C/G]TGCCATGCCCACACA	9972
rs544859988	in-del	-/A	0.0532157	0.154195	intron-variant	NUP153	GRCh38.p7	6:17703198	ACGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	9972
rs544888128	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17690162	TTGAGACCATCCTGG[C/T]TAACACAGTGAAACC	9972
rs544924254	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679800	AACAGCCATTCTTCG[A/G]TGCTCTCATAATAGG	9972
rs544930229	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619266	TCTTACCAAACATGG[A/G]GAGAGAATAAAGATC	9972
rs544951235	snp	A/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17696218	GACTGGCAGTTTTTT[A/T]AAAGAGTTTTGAAGT	9972
rs544960908	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644661	TAAAAAAACAAATTC[A/G]GCCAGGCACAGTGGC	9972
rs545014510	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695791	AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCG	9972
rs545021688	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17637854	TATTACTGAGAAGAC[A/G]TTTACCTCACTGCAC	9972
rs545037380	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679538	TTCATATGGAATCTC[A/G]AGGAACCTCAAAATG	9972
rs545039776	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656138	TGAACTCAGGAGGTG[A/G]AGGTTGCAGTGAGCC	9972
rs545053352	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631250	TCATATAGACATATA[C/T]GCTGTGCAGGTGATG	9972
rs545120205	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17631139	AATTTAGCAGGCTGC[A/C]ACCAGCACTTCTCTT	9972
rs545141342	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708444	ACCTCCTGGGTTCAA[A/G]CGATTCTCCTGCCTC	9972
rs545213068	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17654125	CAACATTTCATGTTT[C/G]AAATTTGTCATAATC	9972
rs545243549	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646348	GAGCAGCTGGGACTA[C/T]AGGAACTCGCCACCA	9972
rs545250088	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663833	GACAAACCCAGATTA[C/T]GGGACATTTTATAAG	9972
rs545255372	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625214	AAACAACTTCCAGTG[C/T]CTGGTTACTGACAAC	9972
rs545283083	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17618834	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA	9972
rs545324708	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17695033	TGAACGAACAAAAAG[G/T]TGCTAAGACCCAAAT	9972
rs545413583	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627326	ATTTCTAAGTAAATA[C/T]ATAACAGACAAAAAA	9972
rs545476568	in-del	-/A	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17657745	ATGTAAAAACTTGTC[-/A]AAAAAAAATAAGCTC	9972
rs545502418	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17681808	TATCCCATTCTCTCA[C/T]CCCTGCATCAGTTTC	9972
rs545537153	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17665650	AGACTTAATGACTTT[C/T]CACACACATGCATGC	9972
rs545538976	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17625165	CCTCATGATGTGCAT[A/G]TATACATTGCATAAT	9972
rs545554993	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639856	TAGTCAGAAATTTTT[A/T]AAAGCCTAAAGTATA	9972
rs545600112	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659458	CACAAGGTAAGACAG[C/T]CCATTTCTTTTGTTT	9972
rs545622512	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614863	CCAGGCAAGAAGTAG[C/G]GTACCTTCTATATGT	9972
rs545625742	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17676467	TGAAGTTACTCCACC[C/T]CACCTTCCCGTTATT	9972
rs545694346	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17669943	GTATTAAAATACAAA[A/T]AATTAGCCAGGCGTG	9972
rs545700333	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17648542	TAACCACTTGAACCC[A/G]GGAGGTGGAGGTTGC	9972
rs545752482	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17648636	AATAAATAAATATTT[A/T]AAAAAAAATTTTTTT	9972
rs545810812	snp	G/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705499	AATATTAAAATATTT[G/T]GTGTATGAGATCAGA	9972
rs545816142	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679978	ATCGCAACCAGATAT[A/G]CTGCCTTGCGTACCC	9972
rs545841024	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658883	AAACTTGCACACAAA[A/T]AAAGGCCATGGTCAC	9972
rs545849500	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641650	CGAGGTCAGGAGATC[A/G]AGACCACCCAGGCTA	9972
rs545861134	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17671926	GGCAGGAAAATTGTG[A/T]GAACCTGGGAGGTGG	9972
rs545880602	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676477	CCACCCCACCTTCCC[A/G]TTATTAAAATATTAA	9972
rs545896931	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695023	TACTATGGACTGAAC[A/G]AACAAAAAGGTGCTA	9972
rs545897389	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17687905	GGATCATGAGGTCAG[A/G]AGATCGAGACCATCC	9972
rs545912762	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634765	CTGAATGTTGACTTC[A/C]GCAGCTTGAAATCAA	9972
rs545957765	snp	A/G	3.3012e-05	0.00406262	missense	NUP153	GRCh38.p7	6:17625825	GCAGAGCTAGATGTG[A/G]TTGTGGCTCCAAAGC	9972
rs546001668	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622181	TTGGCTGGGCACAGT[A/T]GCTCACGCCTGTAAT	9972
rs546051350	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704155	AAATTAGCTGGGCGT[A/G]GTGGCGGGCGCCTGT	9972
rs546053145	snp	A/C/G	3.51465e-05	0.00419192	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706248	AGTTTCCCCACCCGC[A/C/G]AGGCCACCGCGGCGT	9972
rs546055006	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685991	CTCCACAAAAAAATT[A/T]AAAAAAATTTGCTGG	9972
rs546068668	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17675392	AAATTACATAATCCA[C/T]AGTAATAACACCAAT	9972
rs546089631	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641208	GTTTCTGTGTGGGAT[A/G]GGGAGAGGAGGGATG	9972
rs546094859	snp	C/G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17699910	TTCAAACTAAGATAT[C/G/T]TGCCTTGTCAGGGAC	9972
rs546112290	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17645892	TAAGTATCTCTAAAG[A/T]TAATTAATAAAAAGC	9972
rs546115258	snp	C/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667307	GCTTTCTTTGCATCA[C/G/T]AATTTCATTACAGAT	9972
rs546133509	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692386	TAGAACTGTGGCACA[C/G]GCCTGTAGTCTTAGC	9972
rs546138587	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17661205	TATAGTCCCAGCTAC[C/T]TGCGTGGCTGAGGCA	9972
rs546195251	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691747	CGAGACTCCAGCTCA[C/G]AAAAACAAAAAAAGA	9972
rs546252403	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17693893	AAAGTGCACCACCAC[A/C]GCGCCTGGCCTAATA	9972
rs546259413	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691401	TTGTAAAAACACACC[G/T]AATACTAGTTACTTA	9972
rs546264375	snp	G/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17641801	AGCTTGCAGTGAAAC[G/T]AGCTTGCACAACTGC	9972
rs546273237	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17681136	CAATATAGATGGAAC[C/T]GCAGAACATCACATT	9972
rs546275306	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17635199	ACTGCAAGCTCCACC[C/T]CCCAGATTCACACCA	9972
rs546310257	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17666400	TGCGCCTGTAATCCC[A/G]GCTATTCAGGAGGCT	9972
rs546322133	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17643402	GCCTGAACCCAGGAG[A/T]CGGAGGTTGCGGTGA	9972
rs546350082	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686757	TATCAAAATGCTGCC[C/T]ACAACTTGCTTCTAA	9972
rs546374292	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621959	AATGAAAAACTTTAA[A/C]ATATTTTTTTAAAGT	9972
rs546399068	in-del	-/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17687879	CAGCACTTTGGAAGG[-/C]TGAGGCGGATGGATC	9972
rs546477280	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702743	GCAAAAAGGTAAAGG[A/G]GTAGGGGAGAAGGCA	9972
rs546495903	snp	A/G	1.6476e-05	0.00287014	missense	NUP153	GRCh38.p7	6:17661682	GTTTAGAAGCAACAA[A/G]GCGTGTTCTTTCTCG	9972
rs546544592	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661439	CAATTCCCTTATTTG[A/G]AAAAGTATGGGTAGT	9972
rs546545766	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678264	GGGAGGCTGAAGCAC[A/G]AGAATTGCTTGAACC	9972
rs546622538	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17642871	AAGGAATGAAGTATT[A/G]AGACATAAGAACCTT	9972
rs546641882	snp	A/G	0.000411872	0.0143446	synonymous-codon	NUP153	GRCh38.p7	6:17649205	GATGGGTGATGGAGA[A/G]GAAGTTGTGATCTCA	9972
rs546686290	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17635443	GTCTCACTCTGTCAC[C/G]CAGGCTGAAGCGCAG	9972
rs546697497	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17672246	TCGGGGGAGGGATGG[C/T]CAAAAGTCCAGAAAT	9972
rs546760309	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673014	CAGATACGACACCAA[A/G]AGCATGAAACCATTA	9972
rs546761257	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683799	AATCCTAGATGGTAT[C/T]TTCTTCCAACGGCGG	9972
rs546766286	in-del	-/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17638685	TCAAATGAAGATTCT[-/C]CCCCAAACATTTCCT	9972
rs546776157	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644080	AAGGTTGCAAACATA[C/T]CAGTCAAATTCTTAG	9972
rs546822782	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690325	GTAAAATAATTGCTT[C/G]AGAAAGCTTGCAGTG	9972
rs546833800	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630718	GGGAGACGAGAGGGG[A/G]GGGGAGACAAGAGGG	9972
rs546868165	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674420	ATAATGTTTATATAC[A/C]CTAAATGAAAAAAAT	9972
rs546884881	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668001	ACACAATAGATTTCA[C/T]AAAATTTTGGTTAAT	9972
rs546895261	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645321	TTTTTTTGAGATAGG[A/G]TCTTGCTCTGTCAGC	9972
rs546901766	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661880	AAATATACAGCTGAA[C/T]GTGATTCTAAAATCT	9972
rs546920967	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632151	AATAAAAGTCAGTAA[A/G]TTCATCTGGGCGCGG	9972
rs546929638	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674798	AAATAAAAGAAAAAT[A/G]AAAAATAAATCAAAA	9972
rs546931409	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17668713	CAGGGCATGATGGCA[C/T]GTGCCTGTAATCTCA	9972
rs546945629	snp	A/G	0.000230681	0.0107372	synonymous-codon	NUP153	GRCh38.p7	6:17674983	TTTTCCAGGATAAAA[A/G]GGAGAATCTCCAAGC	9972
rs546982598	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17629911	AAATTACAAATGCAT[A/C]TACCCTTTGACCTTG	9972
rs546987572	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17619580	GAACAAAGAAGATTA[C/G]CATGGCCCCCTGCAC	9972
rs546989949	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637942	TTTATCAATTACCTA[A/G]TAAGTTACACTTAAA	9972
rs546992813	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669142	GGAGTGCAGTGGCGC[A/G]ATCTTGACTCACTGC	9972
rs547007017	snp	A/G	0.00993419	0.0697739	intron-variant	NUP153	GRCh38.p7	6:17691660	ATCCCAGTTACTAGA[A/G]AGGCTGAGGCAGGAG	9972
rs547072265	in-del	-/CTTTTT	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17691309	CCAATTCACTGTTCC[-/CTTTTT]CTTTGCTAATATTAC	9972
rs547083972	snp	A/C	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17662930	ACAAAACAACAAGAA[A/C]AAAAAACAAAAGGAA	9972
rs547178682	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689677	AATTAGCTGGGATTA[C/T]ACCACACCCAGCTAA	9972
rs547217879	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663365	CTCCTGGGCTCTCAC[A/G]TGATCCTCCTACCGC	9972
rs547221102	snp	A/G	1.6473e-05	0.00286988	missense	NUP153	GRCh38.p7	6:17637419	TCAGGTTTATTTTGC[A/G]CTAAACAGGTATCAC	9972
rs547224356	snp	A/C/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17696430	GCATGAGGGAAATAA[A/C/G]CTTTCTGTATGGACC	9972
rs547238259	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17642044	GGTAAAGTACTTTTG[-/A]AAAAAACCTTTCCCT	9972
rs547349977	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17702003	AAAGGGCAAAAATAA[A/G]TGGTTTCCTCTCACC	9972
rs547350350	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678850	CTCAAGGAGGCTGAG[A/G]TGGGAGGATCACTTG	9972
rs547377463	snp	G/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704541	ATCTTAAATCTGCTC[G/T]CAAATACCCCTTTTC	9972
rs547380572	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624223	GGGTAACTTCCTAAC[A/G]CAAATCCAATCATAA	9972
rs547424657	snp	C/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614626	ATTGTGGTTTGGGGG[C/T]GGGAGAACTGGGGGG	9972
rs547430642	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707524	ATAAAGCTGTTGTGA[G/T]GAGCAGACGTGATCA	9972
rs547437062	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17663346	AGTTCACTTTAGCCT[C/T]GAACTCCTGGGCTCT	9972
rs547443249	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17618393	GGAAAACTGACTCAG[C/T]AAAGAAACAAAATTT	9972
rs547444412	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17686689	GTTTTAAAAGTTAAG[-/A]AAAAAAAAACAGTAC	9972
rs547458205	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700978	TAATCCCAGCACTTC[A/G]CGGGAGGCCAAGGCA	9972
rs547499660	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657333	GGATCACTTAAGGCC[A/T]GGAGTTCGAGACCAG	9972
rs547504037	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618761	TTAGTAGAGATGGGG[C/T]TTCACCGTGTTAGCC	9972
rs547518902	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17700273	ATTTTTAATAACTCC[C/T]TACCTATATACATAT	9972
rs547574967	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632265	GAGATCGCGCCCCCG[A/T]ACTCCAGCCTGGGCA	9972
rs547584253	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17638880	CTACTGGACTCCTGT[A/G]GGCAGTATACTTATC	9972
rs547620363	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619628	TTGTGAAGTGTTCTA[A/T]ATTTTTAAACTAAAA	9972
rs547662805	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17645042	GTGAGCCAAGATTAC[A/G]CCACTGTACTCCAAC	9972
rs547664660	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651710	AGTTTTTTTTAAAAG[G/T]ACACTTAATAATATT	9972
rs547729551	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645634	TCTTCGGTTCAGAAA[C/T]TATGTATCACAATCT	9972
rs547732092	in-del	-/CAA	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17624054	CAATTAGAAAAAAAT[-/CAA]CAACAATTTTAAGAA	9972
rs547732823	snp	A/C			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704532	TGAATTCTAATCTTA[A/C]ATCTGCTCGCAAATA	9972
rs547738170	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681320	GTTACCAGAAGGCGG[C/T]TCATGCCTGTAATCC	9972
rs547777369	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694707	TGGGGCTGGGGCCAC[A/G]GTGGCTTACTCCTAT	9972
rs547783465	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17676050	CCAGTTGATTAAACC[C/T]ATTCACTTTTTTGAT	9972
rs547794419	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17620791	AGCCAAAAGATAGGA[-/C]CCCCCCTGGCCTAGG	9972
rs547800508	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680772	TCAAAAAGGCAATAA[C/T]GGATGCTGGTGAGGA	9972
rs547805276	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658982	AGAAGTCTGCTCAGC[A/C]AATCAATGAGATGCA	9972
rs547809109	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631899	ATGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	9972
rs547814498	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17652751	CAGCTGGCTGGGTGC[A/G]GTGGCTCATGGCCTG	9972
rs547850233	snp	A/T	0.000399281	0.0141238	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639952	ACCAGGGCTTTTCAG[A/T]ATATCTAGAACACTT	9972
rs547875325	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17672319	CTGGTGGTTCATGCT[G/T]GTAATCCGAACACTT	9972
rs547878905	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660710	TCTATTGTCATATGG[C/T]GGAAATGTTGAACTG	9972
rs547950007	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670398	TTGTATCCTGTGACC[C/T]TGTTAAACTCGCTTA	9972
rs547994895	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17626770	CCTTCTTCCCAAAAT[G/T]TCTTGTGTGGTTTCC	9972
rs548012060	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664730	TGGGTACATGCTAGA[A/G]TTTACTAGTCAACAC	9972
rs548014317	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17670880	CGGTGGCACAATCTC[A/G]GCTCACTGCAACCTC	9972
rs548031852	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658532	AGTTGACAATAACCA[A/G]TCACTGGAAGTTGAC	9972
rs548079038	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639307	TGGTCTTCAACTCCT[A/G]GCCTCAAGTGATCTG	9972
rs548088109	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692626	TTCAATACCCTAATA[C/T]ACCTTTGTAGGTTAA	9972
rs548109925	snp	C/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614823	GTACCTAAGTCGATA[C/T]GCAAATTAGGCATGA	9972
rs548114107	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17641413	GGTGGTACACACCTG[G/T]AGTCTCAGCTACTCA	9972
rs548124511	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633934	ATCCCCAAAAAACAG[A/T]TTCCTAATCTACACC	9972
rs548218826	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653739	TGGGGTAGGAGGTGA[C/T]GGCAACTGACTGAGA	9972
rs548258617	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658289	TAATCACAGTTACTC[A/G]GGAGGCTGAGGCACA	9972
rs548303258	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661232	GGCACAGGAATTGCT[C/T]GAACCCAGGAGGCAG	9972
rs548306523	snp	A/C/G	0.00478372	0.0487162	intron-variant	NUP153	GRCh38.p7	6:17693565	CCATTAACCACCAGC[A/C/G]TATCTCTAAGTAGAC	9972
rs548376161	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681383	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	9972
rs548471013	snp	A/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17698795	AATCACTTGAATCCC[A/G]GAGCGGGGCGGAGGT	9972
rs548489929	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648265	CCATGACAGAGGGAA[C/T]TGCTTGAACGCAAGA	9972
rs548503422	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672028	TAAAAAAAGCAATTC[C/T]AATCAAAATCCTAGC	9972
rs548525234	snp	A/T	0.0609234	0.163554	intron-variant	NUP153	GRCh38.p7	6:17628622	TTGTAAAAAAAAAAA[A/T]AATAATAATAATAAT	9972
rs548536884	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628444	TGTATTTCTCAAAAT[C/T]AGATCCACAGATGAC	9972
rs548573415	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698331	AGCACCGTGGCTCAC[A/G]CCTGTAATCTCAGTG	9972
rs548574877	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621424	TTTAGTGCAGCACTA[C/T]TCACAACAGCCAAGA	9972
rs548632393	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702691	CAAAAAAAGAAAGGA[A/G]AAAAGAAAAATGACA	9972
rs548645165	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691227	TGCAAATTTTCAATA[C/G]ATCTACAAGTAAGCT	9972
rs548695841	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702450	GAGGCAGAGCTTGCA[C/G]TGAGCAGAGATCGTG	9972
rs548699314	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616301	GGGGGAGTAGACTCA[C/T]ATTGGTATATACATT	9972
rs548715589	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17673104	CTGGGCGCGGTGGCT[C/T]ACGCCTGTAATCCCA	9972
rs548790992	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17624014	CTTATATTTTACACC[A/C]CTTTCTACATAATAT	9972
rs548800670	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617672	ACATGGCGAGATCCT[A/C]TCTCTATAAAAAATT	9972
rs548863799	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618178	TAACATCCAAACTTT[C/T]CCAAGTAAAATAATG	9972
rs548877747	snp	G/T			missense	NUP153	GRCh38.p7	6:17675657	CCGAGGATGTAGATG[G/T]CTGACAGTGTAATGC	9972
rs548878747	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684620	TCAATAACTTTTCCT[C/T]TGCATTCACAAGTTG	9972
rs548917721	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683700	ATTGGCTTCAACTTA[C/T]AGTCACCAGTTGCAT	9972
rs548941288	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624003	TACACTGTTCACTTA[C/T]ATTTTACACCCCTTT	9972
rs548948882	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694998	AAAAAAAAAAAGAGA[A/G]AGTGGGAAGTACTAT	9972
rs548976313	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17643434	CTGAGATTGTGCAAC[C/T]GCACTCCAGCCTGGG	9972
rs548978521	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635540	CTAAGTAGCTGGGAC[C/T]ATAGGCGGGTGCCAC	9972
rs549028726	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696530	AGAGGCCGAGGCGGG[C/T]GGATCACAAGGTCAG	9972
rs549037998	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636285	GGTCTCAGTGAGCCA[A/G]GATTGTGCCACTGCA	9972
rs549038735	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673561	GATATTTCACCAAAA[A/G]ATAGGCTGATAGCAA	9972
rs549043389	in-del	-/A			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704292	CGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	9972
rs549065773	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630101	TTTTCTAACAAGGTA[A/T]AAGGAAGTAAGAATA	9972
rs549096957	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17656288	CTCAGAAATGTGGAC[A/G]TTATAACTTCAGGGT	9972
rs549097299	snp	C/T			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632421	CAATGACACAAGAAA[C/T]TTTTTTTCCCACCTG	9972
rs549104318	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17654519	TACAGACAGGGTTTC[A/C]CCATGTTGGCCAGGC	9972
rs549107904	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17688871	TAATCCTTAAAAAAA[A/C]CCCAAAAGGCCATCA	9972
rs549138079	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668137	CTGGAGTGCAGTGGC[A/G]CGGCCTCGGCTCACT	9972
rs549144664	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637987	ACAAAAGATGTTTTG[C/T]TTACAGGATATCACC	9972
rs549163657	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650814	AAAGTACACATTGAA[A/T]TTACAGCCTCTCCAG	9972
rs549186052	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17689623	CTCACCACAACCTCC[A/G]CCTCCTGGGTTCAAT	9972
rs549187582	snp	A/G			missense	NUP153	GRCh38.p7	6:17629530	GAAGATGAGGAAGAT[A/G]TGTCAAAGCCTACAA	9972
rs549201218	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661955	AAAAAGGTACATGTA[A/C]ATTAAATACAGACCT	9972
rs549211422	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17655136	TTTTTAACAACACAC[A/G]CAAAAAAACTCATGG	9972
rs549269253	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631794	ACATGGTGAAACCCC[C/T]GTCTCTACTAAAAAC	9972
rs549301833	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663458	TTCTAGAGATAAGGT[A/C]TTGCTATGGTGCCTG	9972
rs549351786	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650177	TCTGAAGGCACAAGA[A/G]CAACCAAAAGCAAGA	9972
rs549386236	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17675853	ACTTTAAGAAAACAC[A/G]TTACAGTATATAATA	9972
rs549405568	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699323	AACATGGTGAAACCC[C/T]GTCCCTACTAAAGAT	9972
rs549483786	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625346	TCGAGCCTGGCCAAC[A/G]TGGTAAAACCCCATC	9972
rs549558726	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695320	AAGGCAAATTTATTT[C/T]AATAAGCTCTTGAAT	9972
rs549595242	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631297	GTTTATTCCTGACTT[C/T]TGGTTTGCAATCAAG	9972
rs549657111	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17678667	AAATTGTCTTGGCTG[A/G]ACACAGTGGCTCACG	9972
rs549658800	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17624929	CAAATGTCAAGCTTC[A/G]TTTCAGACTCTTACC	9972
rs549666449	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17701606	GCGGAGGTTGCAGTG[A/G]GCCGAGGTCGCACCA	9972
rs549700623	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652510	ACAGGAAACTATCTT[C/T]GTAGCCCGGGGATAG	9972
rs549732664	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699431	GAGGTTGCAGTGAGC[C/T]GAAATCGCACCATTG	9972
rs549769880	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676125	ATCATTCTGAGACCA[C/T]AAAAAATAAGTTTTA	9972
rs549774073	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677321	TTCAGAGGAAGATGA[C/G]AGAACCAAGAGTCTC	9972
rs549831151	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705730	AGGGCCACAGGCAGG[A/G]GAAACCGAGAATTAA	9972
rs549844555	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636945	GAGGAGGTCGTCATA[C/T]ATACCAGACTAGTTA	9972
rs549869401	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NUP153	GRCh38.p7	6:17651871	GGCCAAGATGGGATG[A/G]TCGCTTGAGCGCAGG	9972
rs549953378	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681965	TAATCCCAGCACTTT[C/T]AGGAGGCTGAGGCAG	9972
rs549956853	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17657837	TTTGCCACTTGATAA[C/T]TGGAATACATTCTTA	9972
rs549969032	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699354	ATAAAAACTTAGCCA[C/G]GAATAATGGTGCGTG	9972
rs550009987	in-del	-/AAG			intron-variant	NUP153	GRCh38.p7	6:17694992	TCAAGGAAAAAAAAA[-/AAG]AGAGAGTGGGAAGTA	9972
rs550014120	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17687958	TCTCTATAAAAAATA[A/C]CAAAAAAAAAATTAG	9972
rs550014510	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681410	GCTAACAGGTGAAAC[C/T]CCGTGTCTACTAAAA	9972
rs550044324	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665454	ATATCTAAATTTTGA[A/C]AATAGCTAACATGAC	9972
rs550055763	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615433	AAACAAAATTGTATT[C/T]ACACAAGTTTCATAA	9972
rs550057560	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17629651	CTTTGAAAGGGCCTA[C/T]TTTGAAGAGTATTAC	9972
rs550067793	in-del	-/AAAAC	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17658400	ACTGTCTCAAAACAG[-/AAAAC]AAAACAAAACAAAAC	9972
rs550094319	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631921	GCAGTGAGCAGAGAT[C/T]GGCCACTGCACTCCG	9972
rs550109027	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686297	GAAGAGTATCCAGTG[C/T]GACAAGATGTGGGGG	9972
rs550211749	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654846	ACTATTGTTACATAT[A/G]AAGAAAGTAAGGCAG	9972
rs550239428	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692545	GAAAGGAGGGAGGAT[A/G]GGAAGAAGGAAGGAA	9972
rs550240821	snp	A/C	0.000219784	0.0104806	intron-variant	NUP153	GRCh38.p7	6:17632859	CCTAAAAAAAAAAAA[A/C]AAAACGGGGAGTGGG	9972
rs550276091	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672938	CTAAAACTATAAAAC[C/T]TGTAGAAGAAAACAT	9972
rs550289939	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647470	GAATATGGACCATGT[C/T]GTTATTATATCATGT	9972
rs550301051	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691915	CTCCTGGGCTCTCAT[A/C]TCAGCCTTCCAAGTA	9972
rs550314497	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17652868	CTCTACTAAAAATAC[-/A]AAAAAAAAAAATTAG	9972
rs550349116	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641308	TTGGGAGGCCAAGGC[A/G]GGCAGATCACGAGGT	9972
rs550384103	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621256	ACACACTGTTGGAGT[A/G]AATGTAAATTAGTAT	9972
rs550392695	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17628558	TATGTTCAGTGTAAA[C/T]CATTAATTGACTTGC	9972
rs550395720	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659067	CTACAACAACACCCA[A/G]TGGCACACTGCACAA	9972
rs550427724	in-del	-/A	0.0633504	0.166319	intron-variant	NUP153	GRCh38.p7	6:17689416	AACAAATAAACAAAC[-/A]AAAAAAAAACAATCC	9972
rs550435743	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17680450	ATACAAAAATTAACT[C/G]TAAATGGATTAAAGA	9972
rs550437283	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680671	ACCTACAGGATGGGA[A/G]AAAATATCCACAAAT	9972
rs550447655	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693800	CTGAGGCAGAAAAAA[C/T]GCTTGAACCCAGGAG	9972
rs550454849	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653254	CGAGGCTCCATCTCA[A/C]AAAAAGAACTGAACA	9972
rs550457046	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659703	GTCTCGATCTCTTGA[C/T]CTCGTGATCCGCCCG	9972
rs550467067	snp	C/T	1.65154e-05	0.00287358	missense	NUP153	GRCh38.p7	6:17629168	TGGGCAGTTCCTCTT[C/T]CTTTTCTTCCTGTCC	9972
rs550504309	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698152	TCTCCCAGGGAGCAG[A/G]TTTTTAATTCTTCAG	9972
rs550510576	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672170	AAGACCTACCGGGAA[C/G]CCTATGGCAATCAAG	9972
rs550521552	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650406	AAGCCACCCGAATCT[A/C]TGGTGGACCTGTAAA	9972
rs550571813	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666689	ACTGTAAAATGAACT[A/C]AATTTATTATGTAAG	9972
rs550575904	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17642614	GGTTCAACTACTGTG[C/G]AAAACAGTTTAGTGA	9972
rs550597361	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648052	ACTTTAAATTCTGAA[A/C]AACACAGAACTGTGT	9972
rs550622467	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655243	ATAAGGTGAAAGGTA[A/G]AAGATCATTCCAAAT	9972
rs550655614	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616386	AATCCTCCAGAATTA[C/T]AGTATGGTAAATTTA	9972
rs550658185	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17641750	GTCCCAGCTGCTCAG[A/G]AGGCTGAGGCAAAAT	9972
rs550675953	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677244	ACAGCACAAAACTAC[A/G]TCTACAGAAGTTCAA	9972
rs550678970	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695878	GCTGGACATGGTGGC[A/G]GGCACCTGTAGTCCC	9972
rs550690555	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698642	ACTTGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG	9972
rs550751706	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17646249	GTCTTACTCTGTCGC[A/C]CAGGCTGGAGTGCAG	9972
rs550755627	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703949	GGTGTTATGCTGTTA[A/G]GACATCATCTCCCCA	9972
rs550783382	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678442	TAAACTCCAAATAGA[A/C]ATAAAGAGTGAATTT	9972
rs550823940	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672855	TAGAAAATAAAATGA[A/G]CCTTGACCAATACCT	9972
rs550921731	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622471	CCCTGTCTCAAAAAA[C/T]TTAAAAAAGGATTTT	9972
rs551087686	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702433	GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC	9972
rs551089133	in-del	-/AT			intron-variant	NUP153	GRCh38.p7	6:17620262	AAAGCTATACTTACC[-/AT]ATATATAGCTATATG	9972
rs551090306	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708267	TTACCCGTGTGAGCC[A/G]CCACGCCCAGCCTAT	9972
rs551096215	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17668199	TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGAGATT	9972
rs551104009	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17632225	GGAATTGCTTGAACC[C/T]GGGAGGCGGAGATTG	9972
rs551126105	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666093	GCCTCTCAAAGAGTG[C/T]TGGGATTACAGGCAT	9972
rs551203661	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17644870	GCAGGCAGATCACGA[G/T]GTTAGGAGATCGAGA	9972
rs551229469	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17697065	TACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	9972
rs551239618	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687075	ATCAGTTTGAGTTGA[C/T]CTTGGCATAAATTCA	9972
rs551269381	snp	C/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17690659	GAAGCAGATTTAGTA[C/G]GATTTCAAAGAAAGA	9972
rs551304464	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618726	GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA	9972
rs551305820	in-del	-/A	0.487796	0.0771549	intron-variant	NUP153	GRCh38.p7	6:17694984	CTCTGTCTCAAGGAA[-/A]AAAAAAAAAGAGAGA	9972
rs551365253	snp	C/T	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637350	GTCAATGTAAGGGCT[C/T]GCTTCACACAAGTTC	9972
rs551370995	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17688788	TACAAATTCTACAGA[A/T]GTGAAATTCTTTCTT	9972
rs551398212	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17695941	GTGAACCCGGAAGGC[A/G]GAGCTTGCAGTGAGC	9972
rs551421626	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17702067	ACTCAAGTTTTTTGT[A/C]GTGGTTACTAAGAAA	9972
rs551428625	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17630554	TGTAGTCTCAGCTGC[C/T]TGAGAGGCTGAGGCA	9972
rs551436370	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695200	CTGTGTAATCTTTAG[C/T]TCTGTAGTTTATATA	9972
rs551479001	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630060	GATAAAATCAAAGGG[A/G]CAGAAAGGGAGTGCG	9972
rs551489479	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17653044	GACTGCCTTAGCTCA[C/G]GAGTTTGAGACCAGC	9972
rs551491478	snp	C/G	1.65124e-05	0.00287331	missense	NUP153	GRCh38.p7	6:17675027	GGATTGAAGAATTCC[C/G]AAGTGACTGCACAGA	9972
rs551556484	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698943	ACCTACAAGATACTA[C/T]CACACTTTTTCTCAG	9972
rs551619384	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701592	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	9972
rs551649690	snp	C/T	4.94686e-05	0.00497311	missense	NUP153	GRCh38.p7	6:17625841	TTGTGGCTCCAAAGC[C/T]GAAACCAGAGGTGGT	9972
rs551678959	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694528	CTGGGCATGATGGTG[A/G]TGCCTGTAATCCTAG	9972
rs551690051	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17657993	AAGTTCGAGCGATTT[C/T]CTTATTCGAGTTCAA	9972
rs551700848	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682760	CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCTG	9972
rs551720925	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17688051	ATGAATTCGGGAGGC[A/G]GAGCTTGCAGTGAGC	9972
rs551724553	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650916	TTGTTATTTTTACAG[C/G]ATGTGGTATGAAAGT	9972
rs551759700	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17690700	GGAAAAAAATGACTC[A/C]GTAGGTACAGAAAAC	9972
rs551760764	in-del	-/TTTT	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707961	GACTTACTATAAATC[-/TTTT]TTTTTCTTTCTTTCT	9972
rs551785682	in-del	-/AAGA	0.00174546	0.0294904	intron-variant	NUP153	GRCh38.p7	6:17649119	TTTAAATAAAGAATT[-/AAGA]AAGAACAAATGTCAC	9972
rs551808010	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706086	CCACACGTGTGCGCC[A/G]CAAGGCTGGGCCTGT	9972
rs551816890	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17652548	TTTCTTAGGACACAA[A/G]GAAGAATAAAAATAT	9972
rs551822000	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664666	TTCAACACCACCACA[A/T]GAAAGAAACAGATAA	9972
rs551853223	in-del	-/CAC	0.000890619	0.0210836	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616054	TATCTGAAAGCAGGG[-/CAC]CACCAGCTGTTGTTA	9972
rs551877685	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653079	GCAACATGGTGAAAC[C/T]CTGTCTCTAATGAAA	9972
rs551881103	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658505	TGAGAAGCATAATGG[C/T]CAGCCACTGGAAGTT	9972
rs551941175	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646501	GTGAGCCACCGCGCC[C/T]GGCCCAAATATAGAG	9972
rs551959058	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17669835	ATGGTGGCTCATGTC[C/T]GTAATCCCAGCACTT	9972
rs551969406	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17623151	AAAAAAAAAAGACGA[A/T]GACAACAGAGGAAAA	9972
rs551976838	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17635781	TCCATTATCTAAAAA[A/G]CCAGTGACTCATCAA	9972
rs552010010	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706463	GAGGCCTTAGAGAGC[C/G]TCCCCCGCCGCCCGG	9972
rs552022541	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664094	ACAAAATCTAGTATT[C/T]CTTACAATGAAATAT	9972
rs552042784	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619041	ACTCCCTACACAAAC[A/G]ATAAAAACAAACCCA	9972
rs552094094	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619074	TCAAGACACATCCTG[A/G]TGTATCAGAACAATG	9972
rs552095923	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671011	AGATAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	9972
rs552097641	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686378	GTGCGCATGTCTTAA[C/T]TGTTAACAAACCTTT	9972
rs552134578	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640665	GTTGTCAGCAAGGCC[A/G]GAGTACAGTGGTGCA	9972
rs552197779	snp	A/G/T	0.000563125	0.0167706	intron-variant	NUP153	GRCh38.p7	6:17632872	AAAAAAACGGGGAGT[A/G/T]GGGGGAGATTTCATG	9972
rs552295356	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687045	CCTTATACATTTAAT[A/G]ATATAATGAATAAAA	9972
rs552301418	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17648773	GCACCACTGCTCTCT[A/C]GCCTCGGCAATACAG	9972
rs552357135	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665845	GTGCGCCACCACACC[C/T]GGCTAATTTTTTTGG	9972
rs552383840	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17660404	TATAATACAACTAAA[A/T]TGAGACTTGCATTCA	9972
rs552411602	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694251	AATGAAGAATAGTAA[C/T]GTTTGCCTTTACCTC	9972
rs552417169	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17665613	TCTAAAATGGCTTCA[C/T]GGATACTCTATATTT	9972
rs552473892	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693657	TTTGGGAGGCCGAGG[C/T]GGGCAGATCACTTGA	9972
rs552506919	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628302	TCCCATAGATTATGG[C/T]AGAAAATACTTCATA	9972
rs552516341	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633812	ACCTAACTGATCTCT[A/G]CATTTTATAGGTATG	9972
rs552545397	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665536	AAGAGGAAAAACTGA[A/T]AATAATGGAACCTAA	9972
rs552557728	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17641671	ACCCAGGCTAACATG[C/G]TGAAACCCCGTTTCT	9972
rs552567821	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620419	TCTTCAGTAAATGGT[A/G]CTTGGAAAACTGGAG	9972
rs552578532	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679349	GTGCACATGGAAACT[A/G]CAAAACAGTACCGAA	9972
rs552587337	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628068	TCACTAATCTGATTA[G/T]CAGCTATGAAGTTCT	9972
rs552634864	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666592	TCTCCAAGTTATTTC[C/T]CCCATTGTTATTTAA	9972
rs552668754	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17662829	CTGAAATCTAATCAT[A/G]AGGAAACATCAGACA	9972
rs552697201	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685452	TACTTGGGAGGCTGA[A/G]GCAGGAGAATGGTGT	9972
rs552732506	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17660386	GCTAAGCTGAAATGC[A/G]TTTATAATACAACTA	9972
rs552750517	snp	C/T	0.00755907	0.0610114	intron-variant	NUP153	GRCh38.p7	6:17654351	TTTGAGACGGAGTTT[C/T]GATCTTGTTGCCCGG	9972
rs552785047	in-del	-/AG	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17636645	TTTGAACAGAGAAAC[-/AG]AAAAAACTCAAAACT	9972
rs552807507	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17683365	TAAATAATGAGACTG[G/T]AAAGTCAAAATGCCT	9972
rs552808298	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17625612	AAATTGCTCCCAAGA[A/G]GTAAATATGTTAAAG	9972
rs552818884	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685863	ATTAAAAAAAAAAAA[A/T]TGACTCACAGGTGGT	9972
rs552835444	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17660176	AAATACCAATAGGCA[C/T]GAAGAAATCTAAGAC	9972
rs552857757	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615907	ACCAGTCTAGCTATT[C/T]ATTTATTTAAAAAAG	9972
rs552862621	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654541	TGGCCAGGCTGGTCT[C/T]GAATTCCTGACCTCG	9972
rs552864551	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647584	GAAATCCAGTTGTTT[C/G]CATTTTAACTTTCAA	9972
rs552875770	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648392	GAGGCCAAGGCAGGC[A/G]GATCACCTGAAGTCA	9972
rs552927918	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648119	CTTAGAGGTGGATAT[C/T]TGTATAAAAAAGTAA	9972
rs553001358	snp	A/C/G	4.9588e-05	0.00497911	intron-variant	NUP153	GRCh38.p7	6:17661639	CTCAAGAGTATATGA[A/C/G]TATACAACCCTACCT	9972
rs553020075	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671793	TGGGCGGATCACCTG[A/G]GGTCAGGAGTTCGAG	9972
rs553051654	in-del	-/A	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17641147	TTTCTATTTACAGAT[-/A]AAAACTAAGATGTTT	9972
rs553074695	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708410	GCTGGAGTGCAATGG[C/T]GCAATCTCAGCAACC	9972
rs553080634	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642277	GAAATTATCAAGAAA[A/G]TGAAAAGACAATCTA	9972
rs553102765	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673197	GATGGTGAGAAACTC[C/T]GTCTCTACTAAAAAT	9972
rs553144304	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635259	GGACTACAGGCACCC[A/G]CCACCACACCCGGCT	9972
rs553159044	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17617597	CGTATAATCCTAGCA[C/T]TTTGGGAGGCCAAGG	9972
rs553166209	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673890	GAAAATGAATGCTCA[C/G]AAAAAACATTCATAG	9972
rs553189980	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702568	GTAATGCCAGCTACT[C/T]GGGAGGCTGAGGCAG	9972
rs553227681	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17668222	CTGAGATTACAGGTG[C/T]GCACCGCCACACCTG	9972
rs553271186	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17633830	TTTTATAGGTATGTT[A/C]TCTTCCATCTTGCCA	9972
rs553299341	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17682841	GAGAATTGCTTTATC[A/G]CAGGAGGCTGAAGTT	9972
rs553328317	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630231	GAAAAAGAGACAATG[A/G]AGAGAAGAGATTGAA	9972
rs553361599	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689036	GCACATGCTTTAAGA[C/T]AAATAAAAATTCAGA	9972
rs553378044	snp	A/C			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707352	AGAAAATATATACGG[A/C]TTCATTAATGTTTCT	9972
rs553507202	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17629729	AGAATGATATCTCAA[C/T]CCTCACAACTATCCT	9972
rs553555478	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656833	CTCTTCATGCCTCTT[C/T]ATGGGCCACATGTGC	9972
rs553577460	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638236	TGTGGTATTCTCTAC[C/T]TTCAGTAAAATCAGC	9972
rs553602882	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17682412	TAAGACAACAATGAA[A/G]TTTGCCTCATCGACT	9972
rs553608707	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17703313	AATTACAAGTCAAAT[G/T]AACACATGCAGAAGT	9972
rs553610587	snp	C/G	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706750	CGACTGGTGGGAGTT[C/G]TTCCGTCGCCCTAGC	9972
rs553715313	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17623425	AATAGAACCCACATA[C/T]AAGAACTCATACAAT	9972
rs553729233	snp	C/G/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17656373	GGCAGTTGGCCAGAA[C/G/T]GAAGAGAAGAGGCCC	9972
rs553733927	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695470	ATAGAATTTTACCTA[A/G]AAGACCACCATTTTA	9972
rs553734914	snp	A/G	1.6821e-05	0.00290004	intron-variant	NUP153	GRCh38.p7	6:17624533	CACAAAACCCATACA[A/G]ATACTAACAGCATCA	9972
rs553753183	in-del	-/CA	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17656809	AAGTCCTTCGACGTG[-/CA]CAGTTGTCTCTTCAT	9972
rs553762598	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679824	TAATAGGTAACCATA[C/T]CTTTTAAAGAATTCC	9972
rs553776769	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617789	GGTCGAGGACGCAGT[A/G]TGCCCTGACTCTGCC	9972
rs553780204	in-del	-/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17682051	CACGTCTACTAAAAA[-/T]TTTTAAAACATAGCT	9972
rs553797380	snp	A/G	0.0329836	0.124112	intron-variant	NUP153	GRCh38.p7	6:17694992	TCAAGGAAAAAAAAA[A/G]AGAGAGAGTGGGAAG	9972
rs553797512	snp	C/T	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17638286	CCAAAACTGCTGTCA[C/T]TGAGTTCATTCACTC	9972
rs553824939	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676345	ACATACTAAACCATA[C/T]TAAATTCCCAGAGTC	9972
rs553834941	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654218	CTCTGTCCAACCTCC[A/G]GCGTAGAACCCTAAA	9972
rs553857071	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631505	CATCATCTACCCCCC[A/C]TCCCATCCTCTCACC	9972
rs553858752	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701275	TGGCTCACGCTTATA[A/C]TCCCAGCACTTTGAG	9972
rs553870902	snp	A/C	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17649579	TACTACAGTTGTACT[A/C]ATATGAAACATAAAG	9972
rs553881725	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17633029	GTTTAAAAAAAAGAA[C/T]AGACCTCTCTTTTAA	9972
rs553914538	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706200	GCTCCACGTGGGGCG[C/T]CGGGGCCTCGAACCG	9972
rs553934180	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650334	ACAATCAGCCAGAAA[A/G]GGAGGTGAGATGCAG	9972
rs553938469	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643817	TTCCTGAGATATAAT[A/G]AAACAAAGTTGTTGT	9972
rs553970132	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17642274	AAGGAAATTATCAAG[A/C]AAGTGAAAAGACAAT	9972
rs553993736	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674417	AAAATAATGTTTATA[C/T]ACCCTAAATGAAAAA	9972
rs553997645	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644335	TAGCACTCACCACAC[C/T]GCTATCACTATACTC	9972
rs554002162	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699035	TGCAAAATCAAGCAA[A/G]CTGAAATATCTATAG	9972
rs554022955	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674684	CTAAGGCAGGAGAAT[C/T]GCTTGAAACCAGGAG	9972
rs554036953	snp	C/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17656912	CAGCAAGCTCAGTCT[C/G]CACAGACTCTAGTTG	9972
rs554049757	snp	A/G	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17630952	CATTAAGAAGTACTA[A/G]GATACTTAAAAGTAT	9972
rs554054297	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17617290	TATCTTCTTTGAAAA[A/G]TGCATTAAAACAACA	9972
rs554067017	snp	A/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17693047	ACTGTGCTAAATACA[A/T]ACAGTTCATAAAATT	9972
rs554073364	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658125	GCAAAGGAGGCTGGG[C/T]GTGATGGCTCACGCC	9972
rs554114644	snp	C/G	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17639285	GGTTTCGCCATGTTG[C/G]CCAGGCTGGTCTTCA	9972
rs554134956	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639652	AAGACATGTCTATGT[A/G]TATCATCAGGTTTAC	9972
rs554136962	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646321	CACGCCATTCTCCTG[A/C]CTCGGCCTCCCGAGC	9972
rs554152459	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681453	AGCCGGGTGTGGTGG[C/T]GGGCGCCTGTAGTCC	9972
rs554160437	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17668869	GAATATTATTTTTCA[A/G]ACATGTTCCCTAATG	9972
rs554198405	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17640304	CAAAAAAATATAAAC[C/T]ATAATTATCGTCCAA	9972
rs554288163	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679531	CCTAAAATTCATATG[C/G]AATCTCAAGGAACCT	9972
rs554292554	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670666	AATGCACTTTATCAG[A/G]TAGAAGGATCTCAAC	9972
rs554318949	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17626267	TCCTACCCTAGAATT[C/T]GCTAGAAAATAGATT	9972
rs554332976	in-del	-/T	0.000664242	0.0182121	intron-variant	NUP153	GRCh38.p7	6:17625786	TCCAATTACAATGCA[-/T]TTTTTTCTTTTGTAA	9972
rs554348164	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651604	ATGGAAAAAGATATG[C/T]CCTGAAACTACTAAG	9972
rs554353808	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665097	GCTATTTTAAAAGCA[C/T]ACCAATTCATAATCA	9972
rs554355352	snp	C/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17676927	AAGCCTTACGCAGCA[C/G]CTGCTATGGAGTTGA	9972
rs554382759	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699696	CAAAAATAGCCAGGC[A/G]TGGTGGCACACACCT	9972
rs554383851	snp	C/G	5.25325e-05	0.00512479	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632617	CAAAAAGGCGCTTTA[C/G]CATCACCTTTATTTT	9972
rs554386524	snp	C/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707136	GCCAAGGGGTACTTT[C/T]GCTGTTCTTGGCTGT	9972
rs554413131	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684925	TGGGTGTGGCTCGTG[A/G]CACCCCAAAACAATT	9972
rs554421082	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665573	TATTCATATACCTAT[A/G]CACATAAATATACAC	9972
rs554451455	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17626258	CTAGAATTTTCCTAC[C/G]CTAGAATTCGCTAGA	9972
rs554540315	in-del	-/A	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17661151	AACCCCATCTCTACT[-/A]AAAAATACAAAAATT	9972
rs554545838	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659779	CCCAGCCGCCAACCC[A/G]TTTCTTAAATATAAT	9972
rs554550072	snp	A/G			missense	NUP153	GRCh38.p7	6:17637668	CTCTCCCCAAACCCA[A/G]TTCCACTAGAAGAAA	9972
rs554574758	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676325	ATTGAGAAGCCACTG[C/T]TACCACATACTAAAC	9972
rs554595382	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661048	GGCAGGGCACGGTGG[C/T]TCTCGCCTGTAATCC	9972
rs554603457	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632051	TTATATAGTAAAATA[G/T]TAAGAGTTCTTTTCC	9972
rs554699693	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677553	GAGCCCTTAAAATTA[C/T]TTTGACTAGGATCAC	9972
rs554728042	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633004	ATAGACAACTGTTCA[C/T]ATTTACATTGTTTAA	9972
rs554736408	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666457	AGGCAGAGCTTTCAA[C/T]GGGCCGAGATTGTGC	9972
rs554754808	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685471	GGAGAATGGTGTGAA[A/C]CCAGGAGGCGGAGCT	9972
rs554855861	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700072	TGCAAGTATTGAATT[C/T]AGTCACCTAAAGGAA	9972
rs554914102	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620724	GCTATTGTTAGTGTT[A/G]ATGTATCTTGTGTTT	9972
rs554971617	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17620044	CAGAGGCTGCAGTGA[C/G]CCAAGATTGCACCAT	9972
rs554976965	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614716	TTGTGTATGTATTTC[C/T]AAGAACTTTAATAAA	9972
rs554983818	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628091	GAAGTTCTTCCTGCT[A/C]TTCAGCTCACAGAAT	9972
rs555040374	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615649	AGCACAAACTCAGCA[C/T]AGAAATCATCCGTTT	9972
rs555051041	snp	A/C	1.75121e-05	0.00295901	intron-variant	NUP153	GRCh38.p7	6:17616515	CTCCATTTCAATAAA[A/C]AATTCTCTTACCCCA	9972
rs555119149	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691139	AGAGCAAAAGCGAGA[C/T]TCCGTCTCAAGAAAA	9972
rs555124273	snp	G/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702593	AGGCAGGAGAATAGC[G/T]TGAACCCAGGAGGCA	9972
rs555134793	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702154	AAAAGGAAATGGAAA[A/T]GGAAGACAGGAACTA	9972
rs555178625	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17622586	ACAGTGTGACTCTAA[C/T]TTTTAGGGCCTCTGT	9972
rs555195638	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641427	GTAGTCTCAGCTACT[C/G]AGGAGGCTGAGGCAG	9972
rs555196123	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708375	TTTGAGACGAAGTTT[G/T]TTCCTCTTGTTTTGC	9972
rs555198974	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696033	AACAGAAAAAGAAAA[C/T]ACTGGAACAATTTTT	9972
rs555206911	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17654964	CAGATAAAAAAACTG[A/G]GGAGGTACACAAGAG	9972
rs555257605	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707659	AACAATAAAAGTATA[C/T]TATATTTGCTCCAAA	9972
rs555291554	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17672377	GAGCCCAGGAGTACA[A/C]CACCAGCCTAGGCAA	9972
rs555334026	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17635819	AACTTGACTGTATCA[C/G]TCCTCTGCTGAAAAT	9972
rs555343143	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17683909	AAATTTGATCCTCAA[C/T]GTTGGAAGTGGGGTC	9972
rs555351400	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666242	TAGCTATGGGCCAGG[C/T]GTGGTGGCTCACACC	9972
rs555481546	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682326	CAGGTCTTTGCCTCA[A/G]TGTTGATGGCTACTG	9972
rs555518204	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643376	ACTCGGGAGGCTGAG[A/G]CACAAGAATCGCCTG	9972
rs555523483	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17671547	AAAAGTCTAACAAAT[-/A]AGTCTAACAAAATAT	9972
rs555530030	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695630	AATATGTGTTTATGA[A/T]GCACAGCCAACTATA	9972
rs555545235	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17688335	CCATAACTAGGTAGT[A/G]TCTTCAAAATTAGGG	9972
rs555569619	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628345	TTATTTTCCAGGTAG[C/T]AGATACCAATTCTGA	9972
rs555606635	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687711	GGGCTACAAAAAGTT[C/T]TGTAATTATGTATTT	9972
rs555614908	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662976	GGAGATGAAGAGACA[C/T]GACAACTAAATGCAA	9972
rs555621908	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673628	ATCATTAGTCATTAC[A/G]GAAGTACAAATCAAA	9972
rs555662213	snp	A/G	0.00914312	0.0669923	intron-variant	NUP153	GRCh38.p7	6:17630713	GAGACGGGAGACGAG[A/G]GGGGAGGGGAGACAA	9972
rs555676066	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656906	TGATGTCAGCAAGCT[C/T]AGTCTGCACAGACTC	9972
rs555729145	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624334	CCCATACTTAAGTCA[C/G]AGTAAAAATTAACAC	9972
rs555734796	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17655459	AATCTTATTATTACT[-/T]TTTTTTTTTTTTAAG	9972
rs555782671	snp	C/T	0.00676609	0.0577691	intron-variant	NUP153	GRCh38.p7	6:17623997	CAATATTACACTGTT[C/T]ACTTATATTTTACAC	9972
rs555795041	snp	A/G/T			intron-variant	NUP153	GRCh38.p7	6:17695576	GTTAACATAAAAGCC[A/G/T]ACCTTCGAGTTGATT	9972
rs555816980	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17701184	GAGCCAAGATGGTGC[C/T]GTTGCACTCCAGCCT	9972
rs555826456	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666463	AGCTTTCAATGGGCC[A/G]AGATTGTGCCACCGC	9972
rs555847847	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630321	TTTAAAAAAGGAAGG[A/C]AACAGAAAAACAGAA	9972
rs555871663	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620738	TAATGTATCTTGTGT[C/T]TGGCCGAAGACAATA	9972
rs555876606	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17668281	GACAGGGTTTCACCA[C/T]GTTGTCCAGGCTGGT	9972
rs555906172	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17681950	GGTGGCTCATCCCTA[A/T]AATCCCAGCACTTTT	9972
rs555943646	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651238	AGTCCAGGAGTTCGA[A/G]GCTGTAGTGGGCCAT	9972
rs555967476	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697667	CACTCCAGCCTGGGC[A/G]ACTGAGCGAGACTCC	9972
rs556006798	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645169	AATCGTTTGAATTCG[A/G]GAGGCAGAGGTTGCA	9972
rs556027580	in-del	-/A	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17649528	AATTTCCTAATTGGT[-/A]AAACTGAGGGAAAAA	9972
rs556116337	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700457	ATCCTATCAACTATC[C/T]AATCCTATCAATGTT	9972
rs556120257	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650401	CATATAAGCCACCCG[A/T]ATCTCTGGTGGACCT	9972
rs556177522	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657190	TGGTGTGACTTTGCT[A/G]TACTGAACAGTTTAT	9972
rs556218038	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697471	CAGACAGGTCACCTG[A/G]GGTCAGGAGTTCAAG	9972
rs556231846	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669956	AAAAATTAGCCAGGC[A/G]TGGCAGTGTGTGCCT	9972
rs556327681	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619217	TTCAAAATTATAAAA[A/C]TGATTTCCAATCTAC	9972
rs556345430	snp	A/C/G	6.59287e-05	0.00574113	missense	NUP153	GRCh38.p7	6:17675324	AACGTTCAGCTTCTG[A/C/G]GGACCACAGAGGTGG	9972
rs556377017	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17638425	CCCGCCAAAGAAAAA[G/T]AAATTAAAAGGAGAG	9972
rs556390215	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17703641	GGACTAAAGAAAGTC[C/T]TTATTTTTAAGATTA	9972
rs556428320	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625195	TAAAGACTGATGTTT[A/G]ATAAAACAACTTCCA	9972
rs556428611	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705900	GTATAAGGGCCATCA[A/T]CCACATCTTTTCCTT	9972
rs556442562	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17639368	ACAAGGGTGAGCCAC[A/C]GCGCCTGGCAAGTTT	9972
rs556460502	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17640385	GGCAACTAGGGCAAG[C/T]CCATCCACTGCATGA	9972
rs556473894	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698446	AAAAAATACAAAAAT[C/T]AGCTGGGAGCAGCCG	9972
rs556475306	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680977	GAGATAATCTGCACT[C/T]GCAGCACTATTCACA	9972
rs556493901	in-del	-/T	0.00164237	0.0286092	intron-variant	NUP153	GRCh38.p7	6:17648645	ATATTTAAAAAAAAA[-/T]TTTTTTAATTAGCTG	9972
rs556514892	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17679326	AGGAATGAACCAAGG[C/T]AAAAGATGTGCACAT	9972
rs556521970	snp	A/T	0.000119111	0.00771632	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632634	ATCACCTTTATTTTT[A/T]TTTTTTTGGCCTTAC	9972
rs556537032	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646343	CTCCCGAGCAGCTGG[A/G]ACTACAGGAACTCGC	9972
rs556538561	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680184	CCTGTCTGGGAAATC[C/T]GCTTGGGTCCGTGTT	9972
rs556548291	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17627547	GTTGCCCAAGCTGGA[A/G]TGCACTGGGCCAATC	9972
rs556599942	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686143	ACAGAATGAGATCTT[G/T]TCTTTAAAAAAAAGA	9972
rs556607904	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664258	ACAAATGTTCTAAAA[C/T]TTACCATTATGATGG	9972
rs556625751	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619803	CATTCTCCATAGAAA[C/T]AGAAACATATCCGGC	9972
rs556648300	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698974	GTAACATGTTTGAAA[A/T]TTGGGAGTAAGAGTT	9972
rs556669168	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17658137	GGGCGTGATGGCTCA[C/T]GCCTATAATCCCAGC	9972
rs556678253	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684840	AAAGAGGGAGAAAAG[A/C]GGGGAATAGCCAGTT	9972
rs556691159	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659756	GATTACAGGCATGAG[C/T]CACCGTGCCCAGCCG	9972
rs556732334	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658604	ACTACACAAGAAGTT[A/G]CCAAAGAACTCAACG	9972
rs556739532	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684154	GGTGCCATGCCCACA[C/G]AGTTTGCAGAACCAT	9972
rs556765388	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671111	ACCTGGTCTAATCCC[A/G]TTAATTTTCATATGT	9972
rs556771904	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17647993	AAGCAAACTGATTAT[C/T]CCAAAGACACTAAGT	9972
rs556785819	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627258	ATTAGACCCTATCAT[A/G]TTTTTGTTGCTTTCC	9972
rs556800882	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690917	GGCCGAGGTGGGTGG[A/G]TCATGAGATCAGGAG	9972
rs556835980	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646651	CAGCATTTTAAATTT[C/T]TCAGGCACTTTTTCT	9972
rs556930155	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679428	ACTAAATATTGTTGG[C/G]ATGTCAATACTATTC	9972
rs556935941	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654610	CAGGCATGAACCACC[A/G]CGCCCAGCTGACCTT	9972
rs557000441	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696613	ATAAAAAATTAGCTG[A/G]GTGTGGTGGTGGATG	9972
rs557016190	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677612	GATAGCATTCCCAAC[A/C]CTGCTTTCCTACCCA	9972
rs557064012	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671601	CTACAAAACACTGAT[G/T]AAAAAAATTTATAAA	9972
rs557071622	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17702589	GCTGAGGCAGGAGAA[C/T]AGCTTGAACCCAGGA	9972
rs557076040	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647741	CCAGTGGCATCTTAG[A/G]TTTGATAAAAATATA	9972
rs557086602	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628004	GAACTTGTGGATCTA[A/G]CTTGGATCACTCTTT	9972
rs557123448	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17645835	AATTTGCTACCATGC[C/T]TATCTCTCTCAAAAC	9972
rs557127546	snp	A/T	0.0256215	0.110247	intron-variant	NUP153	GRCh38.p7	6:17666004	TTTTTTTTTTTTTTT[A/T]AATGGAGACTAGGTC	9972
rs557136892	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17641581	AAAAAGGCCAGGCAG[C/T]GGTGGCTCACGCCTG	9972
rs557184603	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697520	GCGAAACCCTGTCTC[C/T]ATTAAAAAATGCAAA	9972
rs557284003	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615693	TCTATACAGAATTCT[A/T]ATCTATACAGAATTC	9972
rs557290593	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17672531	CAGTGAGCCATGATC[A/G]TGCCACTGCACTCCA	9972
rs557346230	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17683417	ATGGACATTGTATTA[C/T]CAAGCATCAGAACAA	9972
rs557374749	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17622330	AGATGGGTGTAGTGG[C/T]GGTGTCTGCCTGTAG	9972
rs557376178	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702303	ACAAGGTCAGGAGAT[C/G]GAGAACATCCTGGCT	9972
rs557512953	in-del	-/T	0.200182	0.244986	intron-variant	NUP153	GRCh38.p7	6:17640783	ACCACATCTAGCTCA[-/T]TTTTTTTTTTTACTT	9972
rs557557475	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627960	TTTCCCCAAAACTTC[C/T]TATCTTCTAGGCCAC	9972
rs557561714	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617714	GCCAGGCGTAGTGGC[A/G]TGCACCTGTAATCCC	9972
rs557594608	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701685	AAAAAAATACAAAAA[C/T]TAGCTAGGCGTGGTG	9972
rs557668181	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17650940	TGAAAGTAACATAAA[C/G]TAATCTGAAAAACAT	9972
rs557671256	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17640673	CAAGGCCGGAGTACA[C/G]TGGTGCAATCATAGC	9972
rs557674649	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17682913	ACAGAGCAAGACTGT[C/T]TCAAAAAAGAAGAAA	9972
rs557680674	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17667598	AGGCGCCTGTAGTCC[C/T]AGCTACCTGCGAGGC	9972
rs557716474	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630398	GGCGTGGTAGCTCAC[A/G]CTTGGAATCCCAGCA	9972
rs557785846	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17677796	GTGCAGTGGCGCAAT[C/G]TTCGCTCACTGCAGC	9972
rs557786246	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17640182	AAAGTTCATGAAAAA[A/G]GTCACTTTAATTCAA	9972
rs557787638	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689239	AAAAATACAAAAAAT[C/T]AGCAGGGCATGGTGG	9972
rs557847612	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17674723	TGCAGTGTGGTCCGA[G/T]ATTGTGCCACCGCAC	9972
rs557852783	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695564	AATCAATGAGAAGTT[A/C]ACATAAAAGCCGACC	9972
rs557867670	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687567	TCTAAAATAAAAACC[A/T]TTCTTTCAGGGCCAT	9972
rs557879054	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682195	CTACACTATAGCCTA[C/T]TAAGTGTGCAACAGC	9972
rs557893189	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17702033	CAGGAGGTGGCAGTA[C/G]GTTCTGGTTTGCCCA	9972
rs557896633	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625053	AAACAAAAACTGCAA[C/T]TAACAACTACTCCAC	9972
rs557912385	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695029	GGACTGAACGAACAA[A/G]AAGGTGCTAAGACCC	9972
rs557923337	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701386	TACAAAAATTAGGCC[A/G]AGTGTGGTAGCTCAC	9972
rs557934200	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17625176	GCATATATACATTGC[A/G]TAATAAAGACTGATG	9972
rs557987361	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706891	TTGCGCCTATTACCC[C/T]TGCTAAGGCGGCTGC	9972
rs557993805	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643735	GGTGAGAACCAACGG[C/T]GTCAAAGTGAGAACA	9972
rs557994857	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17693941	TGCATGGCCTCTTTA[C/T]TTTTTCAGGTCTTTG	9972
rs557998801	in-del	-/CA			intron-variant	NUP153	GRCh38.p7	6:17663930	AAATAAAAACATGTC[-/CA]CACACACACAAACAC	9972
rs558064562	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17651491	ATTTGGTGTTCCAAT[C/T]AAAACACAGAAAATG	9972
rs558095186	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664129	CAGCCATAAAAAGGG[A/G]AAAAATGAAGTACTG	9972
rs558098093	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17684442	CTTCACAGAACTGAA[A/G]GGAGTTAGGGCTTGC	9972
rs558127975	snp	A/G	0.000798403	0.0199641	missense, intron-variant	NUP153	GRCh38.p7	6:17651905	TCGAGATCAGCTTGG[A/G]CAATACGGTGAGACC	9972
rs558137897	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17674110	ACGTATATGACATTC[C/T]GGAAAGGCCAAAACT	9972
rs558160964	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17645390	CCTTGAATTCCTGGG[C/T]TCAAGCAATCCTCCC	9972
rs558198083	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17621133	CTCAACATCACTATC[A/C]TAAGGGAAATGCAAA	9972
rs558202828	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674612	CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCTG	9972
rs558225219	in-del	-/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708646	GCCCAGCCCACTGAT[-/C]CTGTTTCTAAGCTTC	9972
rs558294752	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618551	AAGAAATAGTGGAAG[A/T]TAAAATCTCTCTTTT	9972
rs558322731	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704830	AGGGGCAAGATCTCT[A/G]CTCACGGCAAGCTCC	9972
rs558328773	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645715	TAAAAACTAGAAATA[A/G]AATCTACTACAACTA	9972
rs558346885	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17676753	TAGGAACATTTTCAG[A/G]CCTTGAACAGAGACC	9972
rs558393612	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639532	AGTGAGTACTGCTCC[C/T]TATGTATATGTTACA	9972
rs558412330	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670563	CTGGCTAGCACCTGC[A/C]GTATGATGTTAAACA	9972
rs558451028	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699565	GTTTTGGCTGGGCAA[A/G]GTGGCTCACGCCTGT	9972
rs558509095	in-del	-/TGGAG	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17627543	TTCTGTTGCCCAAGC[-/TGGAG]TGCACTGGGCCAATC	9972
rs558514957	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705301	TAACATTTTCCTATT[C/T]AATACTTCTAACAAT	9972
rs558522429	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17645239	CAGAGCGAGACTCTG[C/T]CTCAAAAAAAAAAAA	9972
rs558559032	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17618715	GGACTACAGGCGCCC[A/G]CCACCACGCCTGGCT	9972
rs558615601	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685614	AAGAAGCTGAAAAAT[A/C]TGTATTCCCTAGTGA	9972
rs558619619	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664850	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	9972
rs558644280	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619862	TAGCAGTTTGGGAGG[A/C]CGAGGCGGGCAGATC	9972
rs558685037	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658708	CAAGCTGAGTGAAAA[C/T]TTAAAAAATTGTTTT	9972
rs558702106	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633461	ATTTATTAAGCATCA[C/T]AATATACTTGGGTTC	9972
rs558815580	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619269	TACCAAACATGGGGA[A/G]AGAATAAAGATCCCT	9972
rs558909767	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17620282	ATAGCTATATGAGAC[C/T]GGTATAAAAAGACAC	9972
rs558929774	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17692774	TAGTAGGATAATCTC[C/T]AGAGGTAGGTCCCAC	9972
rs558973002	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621008	TGAGCTCAAAGAACT[C/G]AACAGCAAAACAAAA	9972
rs558988699	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692162	TCAAAAACAACTGGA[A/G]AACATAACTGGTCAA	9972
rs558997345	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	NUP153	GRCh38.p7	6:17614641	CGGGAGAACTGGGGG[G/T]GGGGGGGAGTGCAGT	9972
rs559004413	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17653081	AACATGGTGAAACCC[C/T]GTCTCTAATGAAATA	9972
rs559031364	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703574	TCCAGTTGACAGCCT[A/G]GGATAATAAACAGCA	9972
rs559053920	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17698413	CCTGGGGAATATGGC[A/G]AAACCCTGTCTCTAC	9972
rs559059904	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653705	ACATGGTGGAAAAAA[A/T]GAGAACAGTGATTGC	9972
rs559080313	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17661911	TAGATTTCTTTATAT[A/G]AAGTTTCTGTTCTTT	9972
rs559111971	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17658611	AAGAAGTTGCCAAAG[A/T]ACTCAACGTTAGCCA	9972
rs559122168	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653373	AATTACAATGAGATA[C/T]CACCACACACAAACC	9972
rs559122304	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17646369	CTCGCCACCACACCC[A/G]GCTAATTTTTTGTAT	9972
rs559123753	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17647185	GGACACAGTCAAAAC[C/T]AGAAAATGACATATT	9972
rs559162095	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17681555	CCACTGTACTCCAGC[C/T]TGGGCGACAGAGCCA	9972
rs559171121	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641238	GGAACAAAAGAAACA[A/G]TAAGAAACAAGATGC	9972
rs559181747	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704665	CGACTGAAAATACCT[A/G]AACCACAATTTTTAC	9972
rs559184354	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646732	AATTTCTGAATGCCA[C/T]TTTCTTTCCTTTTTT	9972
rs559245057	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17695740	GGGGGCTGGGCACGG[C/T]GGCTCACGCCTGTAA	9972
rs559248170	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678582	TGCTCTCCTCAGTAA[C/G]TATTTTGTGATGTGC	9972
rs559284310	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677841	TGTTTGATATTACAA[A/G]TGGGATCCTTTCTTC	9972
rs559306004	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695158	CAAAATTCCCTTTAA[A/G]TTGTGTGCATACCCA	9972
rs559307789	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701751	GGCAGGAGAGCTGCT[G/T]GAACTCGGGAGGCAG	9972
rs559309102	in-del	-/TTTA	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17664304	ACTCACAGACACCAC[-/TTTA]TTTATAAAGTGTTTT	9972
rs559347378	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17689368	CTCTAGCCCGGGCAA[A/C]AAGGGCAAAACTCCA	9972
rs559349341	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641246	AGAAACAATAAGAAA[A/C]AAGATGCGGCCAGGC	9972
rs559410345	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672637	AAAGAACAGTCTTTT[A/T]AACAAATAACACTAG	9972
rs559415284	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17633854	CTTGCCAACCAAATT[A/G]CTCCCTGGGGTTCCA	9972
rs559473897	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17667271	AGAAGCAACACTCTT[C/T]CAATAAAAAGTTCAA	9972
rs559601689	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707099	GGGGAAGGAGATCTC[C/T]GGGGCGCCGCAGAGG	9972
rs559624479	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17688713	CCAAGCAAAACACAA[C/T]GGTGTCCAACAAGTT	9972
rs559626736	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17641684	TGGTGAAACCCCGTT[C/T]CTACTAAAAATACAA	9972
rs559679164	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17616285	AGGGGGGTCGGGTGG[G/T]GGGGGAGTAGACTCA	9972
rs559715901	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681369	AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	9972
rs559716391	in-del	-/TAAAG	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17650936	GGTATGAAAGTAACA[-/TAAAG]TAATCTGAAAAACAT	9972
rs559731428	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698034	ACATTATCCTTAGCA[A/G]TGTTCAGATTATAAA	9972
rs559819880	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700830	CAAAACAAAGGACAA[C/T]TTACCACAGCAAAGC	9972
rs559830518	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681720	TTACATACACATAGG[C/T]TGAAATGTTTCCCAG	9972
rs559845767	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17665159	GTTGCTAGAATACAA[A/T]GGTAGTTATATTTTA	9972
rs559845910	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628296	AGGCCTTCCCATAGA[C/T]TATGGTAGAAAATAC	9972
rs559869302	snp	A/G	8.24323e-05	0.00641945	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706430	GGGGCGGGTAAGGGG[A/G]CGGGAGAGGCAGAGG	9972
rs559907965	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621996	TTTTTATCAAAAATG[C/T]TTTTGGATTATTACT	9972
rs559909742	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660718	CATATGGTGGAAATG[C/T]TGAACTGCAAAACTA	9972
rs559956028	snp	A/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614735	AACTTTAATAAACAC[A/T]ATCCAGTAACTTACC	9972
rs559973535	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655093	GCTACATGTTTTGTA[C/T]ACTGCTACATGTTTT	9972
rs559976005	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17654198	TTTGTAGGGAAGCTT[C/T]TCTTCTCTGTCCAAC	9972
rs559981600	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636665	AAACTCAAAACTAAC[A/T]CCATGTTTCTGGCTG	9972
rs560086326	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699062	ATAGATAGAAAAGGC[A/G]TCCTATCATCCTGTT	9972
rs560114703	snp	A/G	0.00478085	0.0486577	intron-variant	NUP153	GRCh38.p7	6:17674300	ATACTCTAAAACAAT[A/G]AAAAATTGTAGTATG	9972
rs560132019	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17648594	TGCACTCCAGCCTGG[A/G]TGACAGGGCGAGACT	9972
rs560134910	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705466	CAAAAGTAACTATAC[C/T]TCTAGAATACGCCTC	9972
rs560140881	snp	C/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17630444	GCGGGCAGATCACCC[C/G]AGGTCAGGAGTTCAA	9972
rs560153841	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686849	AAGATCAACCGTGAC[C/T]TGATTATTGTTGAAG	9972
rs560197255	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17642923	AGAACTCAGCTGTAC[A/G]AAGCCACATTGTATG	9972
rs560239916	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657592	AAACCTGGTGCCATG[A/G]TATTGGCTTCTGTGC	9972
rs560257744	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643403	CCTGAACCCAGGAGA[C/T]GGAGGTTGCGGTGAG	9972
rs560276823	snp	A/G	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17622287	AAACCCTGTCTCTAC[A/G]AACCACGCCCCCCTC	9972
rs560312888	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17677115	AACTAAAATAAGACC[G/T]ACTACAGATCTCTCC	9972
rs560351868	snp	A/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17673474	AAAATGAACTCTCTC[A/T]AAATTTATTAATAAG	9972
rs560360596	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17657050	TAGCCACTGATTTCT[G/T]TAATTCTTTGGAGCA	9972
rs560376201	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699760	GAATCCCTTGAGCCT[C/G]GGAGGCAGAGACTGC	9972
rs560410069	in-del	-/TAAC	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17703389	CTGGCAAACATCCAT[-/TAAC]TAACAGCGCCAGACC	9972
rs560413185	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17668020	ATTTTGGTTAATGAG[C/G]AAAGTATACAAAGAT	9972
rs560415693	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686208	AACAGCCTTAGGTAA[C/G]TCCTTCTGGAAGTAT	9972
rs560423818	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650736	AAGACATGAGGAATA[C/T]GTGAGCAAACAAAAA	9972
rs560429335	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17646264	CCAGGCTGGAGTGCA[A/G]TGGCGCAATCCTGGC	9972
rs560437677	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699242	TGGCTCAAGCCTGTA[A/G]TCCCAACACTTTGGG	9972
rs560466392	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668332	TGATCCACTGGCCTG[A/G]GCCTCCCAAAGTGCT	9972
rs560533380	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697824	GGGGAAGGCTATTCT[A/G]TAACACTAACTCAGA	9972
rs560533423	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703794	CTTCCCAATTCAAAA[C/G]CTAAAATATGTTTTC	9972
rs560550652	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656571	TTGTACACGTGGGGT[A/T]TTGCCATGTTGCTCA	9972
rs560593564	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703135	CCCAGGAGGCAAAGG[C/T]TGCAGTGAGCCAAGA	9972
rs560602577	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679861	TGCTCTTAGGAGATC[A/C]AAAATCAAACCAAGG	9972
rs560634399	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663950	CACACAAACACACAA[A/G]AAAACACTTATACAT	9972
rs560645591	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17691707	GAGGCAGACGGGCCA[C/T]TGCACTCCAGCCTGG	9972
rs560682877	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17675830	ATACACTACCACAAA[C/T]GGTTTTTACTTTAAG	9972
rs560697751	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664425	GGCCAGGGTGAGGGT[C/T]TGAGGTCTGGAAAAA	9972
rs560713702	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631706	GCGTGTTGGCTCACG[C/T]CTGTAATCCCAGCAC	9972
rs560732954	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17685781	TGGTAATGATAATAA[A/C]TGACTATGTAACTGT	9972
rs560754692	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678767	TGGGCAACATACTGA[C/G]ACTTCATCTCTACTA	9972
rs560834028	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17636882	GATCTTTCAGAATCT[G/T]TATTAGTCAACTTTG	9972
rs560836927	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17674804	AAGAAAAATAAAAAA[C/T]AAATCAAAACTATTT	9972
rs560863523	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695050	GCTAAGACCCAAATA[C/T]AGGCGTGTCCTTGGA	9972
rs560865926	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17701268	GGTGCAGTGGCTCAC[A/G]CTTATAATCCCAGCA	9972
rs560869668	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631251	CATATAGACATATAC[A/G]CTGTGCAGGTGATGG	9972
rs560874742	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17678134	GCCAAGGCGGGCAGA[C/T]GACTTGAGGTCAGGA	9972
rs560911842	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17638524	TAAGGACAAAATACC[A/G]CATGCTTGAGTTATT	9972
rs560935710	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658271	GCCTGTGGCACATGC[C/T]TGTAATCACAGTTAC	9972
rs560987495	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618858	GGCGTGAGCCACTGC[A/G]CCCAGCAGAAGTTAA	9972
rs560996624	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652431	AATCCATGGGTCAAA[C/T]ACAAAAATCAAAAGA	9972
rs561029220	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17633200	CTAAATTTTTCTTAA[G/T]AATCTTTTTCAAATT	9972
rs561040498	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657597	TGGTGCCATGGTATT[A/G]GCTTCTGTGCTCATC	9972
rs561047189	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619354	AAGATGTGCTGTATC[A/T]GAAAATAGGGGAGTA	9972
rs561059589	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625688	ACAACCCTGGTATAG[A/G]TGACCAAAAGGCATT	9972
rs561104682	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17654375	TGCCCGGGCCGGACT[A/G]CAGTGGTGCGATCTT	9972
rs561172770	snp	G/T			missense	NUP153	GRCh38.p7	6:17629277	ATCATTCTTACTATC[G/T]TTTTTAACTTCTTCG	9972
rs561222660	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677257	ACATCTACAGAAGTT[A/C]AAAATTATCATTAAC	9972
rs561253872	in-del	-/ACAT	0.00142592	0.0266632	intron-variant	NUP153	GRCh38.p7	6:17651963	GCGAGGTATGATGGC[-/ACAT]ACATGCCTGTGGTCC	9972
rs561264688	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621142	ACTATCATAAGGGAA[A/G]TGCAAATCAAAACCA	9972
rs561271179	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17646396	GTATTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	9972
rs561318168	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17626822	AAGTTTAGCTTGTCA[A/G]GCTCTACAAAAATTC	9972
rs561329065	in-del	-/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17664990	CCCGGGAGGCAGAGG[-/T]TGCAGTGAGCTGAGA	9972
rs561331045	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691039	CCCAGCTACTCAGGA[G/T]GCTGAGGCAGGAAAA	9972
rs561334346	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640589	TACATAACAGTGACA[A/T]GATGAAATACTTATG	9972
rs561454312	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17689693	ACCACACCCAGCTAA[A/T]TTTGTATTTTTAGTA	9972
rs561490023	snp	A/G	0.000152108	0.00871957	intron-variant	NUP153	GRCh38.p7	6:17665406	AGGTAAAGAGAAATC[A/G]AAAACATTTATTTTC	9972
rs561514080	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708628	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCCACTG	9972
rs561540200	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641716	ACAAATTAGCCGGGC[A/G]TGGTGGCAGGCGCCT	9972
rs561562138	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17672674	GCACACCCATATGTT[-/A]AAAAAAACAAAAAAC	9972
rs561579447	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708062	TTGGCTCACTGCACC[C/T]TTTGCCTCCCAGGTT	9972
rs561585876	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627519	GGGTTTTCTTGAGAC[A/G]GAGCCTTGTTCTGTT	9972
rs561616234	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659641	TCACACCCAGCTAAT[C/T]TTTGTATTTTTAGTA	9972
rs561669460	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701513	CTAAAAATACAAAAA[G/T]TAGCTGGGCGTGGTG	9972
rs561731155	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706988	GAGCTGATAGGCAAA[A/G]AGGAAGGGCTGGTCG	9972
rs561736872	in-del	-/TCATGT			intron-variant	NUP153	GRCh38.p7	6:17685239	ACAGCAGATATATAG[-/TCATGT]GCCACATAAGAACAG	9972
rs561755081	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697857	TCACTTGTAATTAAC[A/G]ACATTCTTTTCTTAT	9972
rs561793265	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695129	AGTAAAACTTAAAAT[A/G]GCTTTAAATCTCACA	9972
rs561794470	snp	A/G	1.69732e-05	0.00291313	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706266	GCCACCGCGGCGTCG[A/G]GGTCCCATACCTGAT	9972
rs561795818	snp	A/C	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17654402	TCTTGGCTCACTGCA[A/C]CCTCTGCCTTCTGGT	9972
rs561798792	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682665	GGCTCACACCTGTAA[C/G]CCCAGCACTTCGGGA	9972
rs561852631	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17628478	ACCAGAATCATGAGG[C/G]TTTTAAAGAGCAGTT	9972
rs561855631	snp	A/G	1.66034e-05	0.00288122	intron-variant	NUP153	GRCh38.p7	6:17647931	AAATTATTAAGAAAT[A/G]ATACAAAAAGAGCTT	9972
rs561858619	snp	G/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705750	CCGAGAATTAACTCA[G/T]AGGCTGAGACTAAGT	9972
rs561944947	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680356	GACCACTCAATGGGA[A/G]AAGGACAGTCTCTTC	9972
rs561949676	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681607	CAAAAATAAAAAACC[A/G]GAGATACTGTCTGGG	9972
rs561984008	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17640759	GTAGCCAGGAACACA[C/G]GCGCATGCCACCACA	9972
rs561997642	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17629778	TATCAGACTGGCTGC[A/G]ATAAAGTTTGATAAA	9972
rs562018767	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656501	CACTTCAGCCTCCCT[C/G]GTAGCTGGGACCACA	9972
rs562029381	snp	C/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645016	CATGAACCTGGGAGG[C/G/T]GGAGGTTGCAGTGAG	9972
rs562037884	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694677	AAAGAAAAGAAAAGA[A/T]AAAGAAATAAAGGAT	9972
rs562075718	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680713	TAAGGGATTAATATC[C/T]AGAACATAAAAAGTA	9972
rs562075823	snp	A/T	0.00200884	0.0316288	intron-variant	NUP153	GRCh38.p7	6:17686719	CTATAGAAAAAAAAA[A/T]TTTTTTAAGTTTTTG	9972
rs562085559	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655219	TCCTTGCACATTTTA[C/G]AATCCAGGATAAGGT	9972
rs562095047	snp	A/G	1.64814e-05	0.00287061	synonymous-codon	NUP153	GRCh38.p7	6:17629109	AGGAGCAGGGGTGGA[A/G]TTAATAACACCTGTA	9972
rs562155750	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622413	GAGGCAGTAGTGAGC[C/T]GAGATTCCACCACTG	9972
rs562168873	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616786	ACGGAGTCTCGCTCT[C/T]TTGCCCAGGCTGGAG	9972
rs562177699	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17689870	AAGTAATGTGGTATA[A/C]TAGCTTTCACTATTA	9972
rs562250006	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617419	CCAAACATACCCAAA[A/G]TGTTTAGGTTCCAGA	9972
rs562375106	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649012	ATTTGTACATTTTTT[A/T]AAAAAAGCAAAACAG	9972
rs562399995	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643450	GCACTCCAGCCTGGG[C/T]GACAGAATGTGCAAC	9972
rs562420963	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674751	CACTCCAGCCTGGGC[A/G]ACAGAGCCAAGACTC	9972
rs562428212	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671350	GTTCCCTACTCTCCT[A/G]CTATACATAAGAGTT	9972
rs562526785	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17698681	AGGCAGAGCTTGCAG[G/T]GAGCCGAGATCGCGC	9972
rs562527629	snp	A/G	1.67287e-05	0.00289207	missense	NUP153	GRCh38.p7	6:17637164	ATACCTGGTTTCTCA[A/G]ACATACAGGACACAC	9972
rs562557786	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693501	GTCCTAGAGAAGGTA[C/G]TAGCGTTCTGCTATT	9972
rs562583957	snp	A/G	1.64757e-05	0.00287012	missense	NUP153	GRCh38.p7	6:17624602	AATGCAGACTGACTA[A/G]GTTGCTGTCCAAACA	9972
rs562585865	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17686063	TGAGGTGGGAGGATC[C/G]CTTGAGCCTGGAAGG	9972
rs562618778	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17699222	TACAAGCTAGCTGGG[C/G]GTGGTGGCTCAAGCC	9972
rs562655087	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631078	TCTAAAACACTTAAA[A/T]GCAGTGTTTTTCAAA	9972
rs562659504	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668562	AATACTATTTTTCAG[A/G]GTCAGGCACAGTGGC	9972
rs562681951	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624045	TATATTTCACAATTA[A/G]AAAAAAATCAACAAC	9972
rs562686413	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671031	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	9972
rs562697259	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17693321	ACCAACTGGTTTCTG[G/T]TAAGACTGCCCCATG	9972
rs562752626	snp	A/T	0.0792508	0.182605	intron-variant	NUP153	GRCh38.p7	6:17663230	TGCTAAAAAGAAAAA[A/T]ATACACACACACACA	9972
rs562808240	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679324	TTAGGAATGAACCAA[C/G]GTAAAAGATGTGCAC	9972
rs562815467	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663778	ACAATAAGGTGTTAA[A/G]TAAACAAAATAAATA	9972
rs562820706	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17649523	GTACCAATTTCCTAA[C/T]TGGTAAAACTGAGGG	9972
rs562853405	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643404	CTGAACCCAGGAGAC[A/G]GAGGTTGCGGTGAGC	9972
rs562864384	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17632118	ATCGCTTTTAATTTA[A/G]AGGTGTATTCCCAGT	9972
rs562903995	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679758	ATGTTACACATGCTA[A/T]CCCTGAGGCTTTAGT	9972
rs562950702	snp	G/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17628088	TATGAAGTTCTTCCT[G/T]CTATTCAGCTCACAG	9972
rs562982828	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17670503	AAATATTACAGGAAT[A/G]ATACCCTTTCCAATC	9972
rs562998540	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685091	ACATGGGATTGCCAC[A/G]AACTCAATTTGTAAA	9972
rs563035193	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17621909	ATTTATTACACATTG[A/T]ATGTATGTAACAAAA	9972
rs563050101	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667971	GAGAGATCTGCCTAA[C/T]TGAAATTCTACTACA	9972
rs563056473	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697089	AAAAAAAAAATTAAT[C/G]TTAAAAAATACTCTG	9972
rs563089136	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658841	AGTGGTTAACCAAGA[A/G]GTAGCTTCAAAGCAC	9972
rs563114806	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702625	AGGTTGCACTGAGCC[A/G]AGATTGCACCATTGC	9972
rs563116746	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625722	ACCATTTTGTGATAA[A/C]CTGCTATATGATATT	9972
rs563152964	snp	C/T	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17697776	GGTGGGGGAAGGCTA[C/T]TCTATAACACTAACT	9972
rs563157826	snp	A/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17664505	GCAATTATGAAAAAC[A/G]TTTCAATATGGACTG	9972
rs563178278	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619488	AAGCCAAGAAAGCCT[G/T]GTAGGAGGAACAGGT	9972
rs563210427	snp	C/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17703074	GTGGTGGCGCATGCC[C/T]GTAATCCCAACTACT	9972
rs563216753	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653549	TAGCACCTCTTCTTC[C/T]AGGTATTTACCCCAG	9972
rs563228481	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671649	TATACCATGTTCATG[A/G]TTTGGAAGACTCAAT	9972
rs563269791	snp	A/C/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17690178	TAACACAGTGAAACC[A/C/G]CGTCTCTACTAAAAA	9972
rs563271811	snp	A/T	0.0337553	0.125452	intron-variant	NUP153	GRCh38.p7	6:17683102	CCACTGAAGTCCTGA[A/T]CCCCTCAAAGTTATC	9972
rs563337166	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17626404	GGAAGGCCTTTGGCA[C/T]TCAGGTTAATAAAAA	9972
rs563380242	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665168	ATACAATGGTAGTTA[C/T]ATTTTACATTATTTA	9972
rs563400540	snp	A/G	0.0103295	0.0711199	intron-variant	NUP153	GRCh38.p7	6:17620124	AAAAAAAAAAAAAGG[A/G]AGGGAGGGAGGAACA	9972
rs563586640	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695804	CATGAGGTCAGGAGA[C/T]CGAGACCATCCTGGC	9972
rs563601209	in-del	-/TG	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17676155	CCCGTATTTTGATAC[-/TG]TGTTGCTTTTATTTC	9972
rs563624647	snp	A/T	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17671366	CTATACATAAGAGTT[A/T]GTGTAGAATTGGTAT	9972
rs563637110	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647051	CATGAGCCACCGTGC[C/T]CGGCCTCAAATGCCA	9972
rs563649052	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701833	GCAAGACTCTGTCTC[C/G]GGGGGGGGGGGAAAA	9972
rs563653496	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685276	CAACTAGTTGGGAGC[A/G]GTGGCTCACGCCTGT	9972
rs563689515	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696253	AAGACTTCAGCCACT[A/T]ACAAATAAGAGTAAA	9972
rs563697951	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641176	TTGGGATTGTTGAAG[A/G]GTGACCTGACATGTA	9972
rs563708680	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621268	AGTGAATGTAAATTA[A/G]TATAACCGTTATGGA	9972
rs563744964	in-del	-/TTAG			intron-variant	NUP153	GRCh38.p7	6:17662181	GAATTTGATGGCTTT[-/TTAG]TTAATGAATCCTGAA	9972
rs563861368	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671899	TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	9972
rs563893774	snp	C/T	0.000115572	0.00760082	synonymous-codon	NUP153	GRCh38.p7	6:17616571	AAATGGAAAGCCCCC[C/T]GAGCCTGAAGGCTGG	9972
rs563910963	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707269	AAATCAAAGACAAGA[A/G]CTAATGATTTAAGAA	9972
rs563924658	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666376	AAAAATTAGCCAGGC[A/G]TGGTGGCATGCGCCT	9972
rs563927949	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648084	ATAAAATGTGGCTTC[C/T]TCTAAGGAGTACACA	9972
rs563947131	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621822	ACATTTCAAAATAGC[C/T]AGAAGTTCTGAAATG	9972
rs563951592	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660318	ACTGGTGAAATTTTA[A/G]TTAGAAACAAATGAC	9972
rs563960718	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17693691	CAGGAGCTGAGACCA[A/G]CCTGGCCAACGTGGT	9972
rs563977267	in-del	-/AAAAC	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17641535	CGAGACTCCGTCTCA[-/AAAAC]AAAACAAAACAAACA	9972
rs564010142	snp	A/C/G	3.37355e-05	0.00410692	intron-variant	NUP153	GRCh38.p7	6:17616222	GTGACATGATGCTCT[A/C/G]AGCAAAATTTCCAAA	9972
rs564063621	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17629978	CATAGACATGCAAAA[C/T]GCCATATGCAATCCA	9972
rs564072983	in-del	-/AAAAG			intron-variant	NUP153	GRCh38.p7	6:17688147	AGAAAGAAAAAAAGA[-/AAAAG]AAAAGAAAATTAAAA	9972
rs564080376	snp	A/T	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17655072	ACTCAAGTCTTCTTA[A/T]ATACTGCTACATGTT	9972
rs564091764	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17622187	GGGCACAGTAGCTCA[C/T]GCCTGTAATCCTAGC	9972
rs564172495	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681843	ATAGGAGAAAAGTGA[C/T]AGGATAATTTTCTAA	9972
rs564177548	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700859	GCCTAAAAATTCACT[A/C]TCTGTGTCCCTTTCA	9972
rs564196719	snp	C/T	0.00438332	0.0466095	intron-variant	NUP153	GRCh38.p7	6:17687916	TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACG	9972
rs564201813	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645911	TTAATAAAAAGCACC[A/G]TCAAAAAGGTTAAAT	9972
rs564220267	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656045	CCCCATCTCTACTAA[C/G]AATACAAAATTTAGC	9972
rs564240997	snp	C/G	0.00217935	0.0329382	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706253	CCCCACCCGCCAGGC[C/G]ACCGCGGCGTCGGGG	9972
rs564242525	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642786	GGTGGAAACAGCCCA[A/C]ATGTCCATTAATGGA	9972
rs564261772	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694593	ACCTGGGAGGCGGAG[G/T]TTGCAGTGAGCCAAG	9972
rs564282837	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656525	GACCACAGGCGCTAA[A/C]CACCATGCCTGGTTA	9972
rs564342176	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649961	TGTGAAACAAGCATT[G/T]AGTAACTGTCAGTAC	9972
rs564384474	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671073	CCTTCCAAAGTGCTG[A/G]GATTACAGGCATGAG	9972
rs564402862	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662351	CAAAATTACTTTACT[C/T]ATCCCTCTTTTTGTC	9972
rs564461570	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17681168	AGTGAAATACACCAG[A/G]CACAAAAAGACAACT	9972
rs564466561	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693289	ATTTTTGATAGGCTG[C/T]TTCTATGGACTGCAC	9972
rs564481742	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17622905	GGAGGCCGAGGTGGG[C/T]GGATCATGAGGTCAG	9972
rs564486015	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705508	ATATTTTGTGTATGA[A/G]ATCAGAGCTGGAGTC	9972
rs564523961	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17661846	ACTTGTTAACTAGAA[A/C]TGCTAACAAGTAAAA	9972
rs564542108	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617553	ACCAACACAAAGATG[G/T]TAATTATCAGTGGGT	9972
rs564552290	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644344	CCACACTGCTATCAC[C/T]ATACTCACATCCATC	9972
rs564567063	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631972	CACCATCTCAAAAAA[A/C]ACACAAAAATCTGGC	9972
rs564571421	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17701429	AGCACTTTGGGAGGT[C/G]AAGGCAGGTGGATCA	9972
rs564589694	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17698599	AAAAATTAGCGGGGC[A/G]TGGTGGTGGGCACCT	9972
rs564629112	snp	C/T	1.6483e-05	0.00287076	missense	NUP153	GRCh38.p7	6:17675588	CATCATGCTGAGAGG[C/T]AGAATCTTTAATTTC	9972
rs564652403	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644797	AAAATACAAAAAATT[A/G]GCCAGGGGCAGGGCG	9972
rs564689725	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17640966	ATGGGTAAAAGCAGG[C/T]TGAAAAGTCTAGAAT	9972
rs564692788	snp	A/C/G	0.000148463	0.00861459	synonymous-codon	NUP153	GRCh38.p7	6:17669520	TGCACTGAGTTGCTT[A/C/G]GCTTTCATTTGTCTT	9972
rs564702655	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680439	TCTTGAACCATATAC[A/C]AAAATTAACTCTAAA	9972
rs564707504	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685481	GTGAACCCAGGAGGC[A/G]GAGCTTGCAATGAGC	9972
rs564714475	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637922	TTTTCACTTAAGTAA[A/T]CATATTTATCAATTA	9972
rs564828480	snp	A/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637384	GTTTCGGTGTTTCAC[A/G]GGCTACACATTTTAT	9972
rs564912272	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17703294	CCCAGAAGTCAAAAC[A/C]GGAAATTACAAGTCA	9972
rs564985325	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669139	GCTGGAGTGCAGTGG[C/T]GCGATCTTGACTCAC	9972
rs564996525	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631693	GCCTCCAGACCAGGC[A/G]TGTTGGCTCACGCCT	9972
rs565013413	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657830	ATAACAATTTGCCAC[C/T]TGATAATTGGAATAC	9972
rs565048130	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625233	GTTACTGACAACCTA[A/G]CATTTTAAAAACAAA	9972
rs565135239	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17678278	CGAGAATTGCTTGAA[A/C]CTGGGAGGCAGAGGT	9972
rs565144092	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17626903	ACAAGTATGCCTTTT[A/G]TGTTCTTTTAGTTAT	9972
rs565216262	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651693	CAAAAAATATTTCCA[A/G]AAGTTTTTTTTAAAA	9972
rs565220755	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679088	AACTAAGACTAGAAC[A/G]AAACTACAACATAAT	9972
rs565226311	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17658195	ATTTGTCAGGAGTTC[A/G]AGACCAGCCTGGTCA	9972
rs565261301	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639869	TTAAAAGCCTAAAGT[A/G]TAATACAAAATGACA	9972
rs565281150	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645484	TTTTTTTTTTTTTTC[A/G]GTAGGGATGAGTCTC	9972
rs565310060	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660601	ATAAGAAATTATATA[C/T]ATATCCCTACAGGAA	9972
rs565454598	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702404	TCCCAGCTACTCGGG[A/T]GGCTGAGGCAGAAGA	9972
rs565505941	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17670337	ATTTCATAGTCACTG[C/T]TGCCAATATATGTAT	9972
rs565524726	snp	C/T	0.000399281	0.0141238	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632791	ATCCTAGAGAGCCTC[C/T]AGAAGGCAGAGAGAC	9972
rs565526707	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702613	CCCAGGAGGCAGAGG[C/T]TGCACTGAGCCGAGA	9972
rs565657594	snp	A/G			missense	NUP153	GRCh38.p7	6:17637401	GCTACACATTTTATT[A/G]CTTCAGGTTTATTTT	9972
rs565691944	snp	C/G			missense	NUP153	GRCh38.p7	6:17661672	TCCTCCAGAGGTTTA[C/G]AAGCAACAAAGCGTG	9972
rs565700920	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671449	GAAGCTTCTTTGCTG[A/G]AACGTATTTTAAATT	9972
rs565711514	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708255	AAAGTGCTGGGATTA[C/T]CCGTGTGAGCCGCCA	9972
rs565770374	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17635301	TTGTTAGTAGAGACA[A/G]GGGTTCACTGTGTTA	9972
rs565859740	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682108	CCAGCTACCTGGGAG[A/G]GTGAGGAGGAGAATG	9972
rs565962720	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17659253	TTCCAAGAGCTTGTC[A/G]AATCCCAAAGCACAG	9972
rs565997479	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	NUP153	GRCh38.p7	6:17614644	GAGAACTGGGGGGGG[C/G]GGGGAGTGCAGTTCT	9972
rs566075241	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620685	AGATTTTTTTTCTTG[A/G]CAATTTTCTTTTTCA	9972
rs566117304	snp	A/C	0.00636936	0.0560724	intron-variant	NUP153	GRCh38.p7	6:17687299	AAACAAATCTCATAA[A/C]CAGGAAACAGAGGGG	9972
rs566140191	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17621332	ATAGAATCACCTTAT[G/T]ATCCAGCAATCCCAC	9972
rs566156083	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659761	CAGGCATGAGCCACC[A/G]TGCCCAGCCGCCAAC	9972
rs566182498	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706003	CATGGGCCTACAATT[C/T]CTTTTCCCGCCCAGA	9972
rs566188897	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615599	GAAAAGTTTAGCGCA[C/T]AATACACCCAACTCA	9972
rs566191615	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619699	GACATCCTATATTCA[C/T]GGATCAGAAGAACTA	9972
rs566193644	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701591	GCTTGAACCCAGGAG[A/G]CGGAGGTTGCAGTGA	9972
rs566217787	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653960	CTGACGTATTTGGGG[A/G]TGAAGTGTACTAATG	9972
rs566262140	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622249	GAGCTCGGGAGTTAG[A/G]GACCAGCCTGGATAA	9972
rs566325549	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622550	CAACCCTAAAATGCT[C/G]TCTTTCCCCAAGTTT	9972
rs566356453	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648210	TCAGGAGCAGGCCAG[C/G]TACAGTGCCTCACAC	9972
rs566367252	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705248	GACACACACTTCCCA[C/T]CTCAGTATCACTGAT	9972
rs566411271	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635455	CACCCAGGCTGAAGC[A/G]CAGTAGCATGATCTC	9972
rs566417688	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17641808	AGTGAAACGAGCTTG[A/C]ACAACTGCACTCCAG	9972
rs566424708	in-del	-/AAACAAACAAACAAAA			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632309	GTCTCAAAAACAAAC[-/AAACAAACAAACAAAA]AAACAAACAAACAAA	9972
rs566449754	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617621	GCCAAGGCAGGTGGA[C/G]TGCTTGAGCCCAGGA	9972
rs566466523	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17686346	CTGATACTGACTTTA[C/T]GTAGGGCTAGGTTAA	9972
rs566474359	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648690	CACCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA	9972
rs566536725	snp	C/G/T	6.59011e-05	0.00573988	missense	NUP153	GRCh38.p7	6:17649219	AGGAAGTTGTGATCT[C/G/T]AGGGGAACTAAAATT	9972
rs566570746	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673044	AAGAATACACACACA[C/T]GCACACACACACACA	9972
rs566595270	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618604	GGAGTCTGGCTCTGT[C/T]GCCCAGGCTGGAGTG	9972
rs566597589	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17643543	TTATAATTTAATCAC[A/G]TTCTATCTTCCTTTA	9972
rs566622968	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682045	AGGCCTCACGTCTAC[C/T]AAAAATTTTTAAAAC	9972
rs566633959	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667453	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9972
rs566639234	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661881	AATATACAGCTGAAC[A/G]TGATTCTAAAATCTT	9972
rs566646047	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686029	AGCACACGCCTATAG[C/T]CCCAACTACTTGGGA	9972
rs566656362	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17632179	CGGTGGCTCACACCT[A/G]TAATCCCAGCTACTT	9972
rs566665432	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644177	GCTTCTATGTCCTGA[C/T]TCTTTTTATTTTTTA	9972
rs566668472	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673177	TTCGAGACCAGCCTG[A/G]CTAAGATGGTGAGAA	9972
rs566681888	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661450	TTTGAAAAAGTATGG[G/T]TAGTTTTGTTTTGTT	9972
rs566700089	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656095	TTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC	9972
rs566705653	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653518	GATGGCTCCTTAGAA[A/G]GTTAAACATACAACT	9972
rs566707076	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692672	TAAGAAAAAGTTAAA[C/T]TAAGCTTAATATAAT	9972
rs566781284	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671255	CATGAGAAATAATAG[C/T]CTGTTGCTGTCTTCT	9972
rs566783358	snp	C/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17698799	ACTTGAATCCCAGAG[C/G]GGGGCGGAGGTTGCA	9972
rs566844512	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698343	CACGCCTGTAATCTC[A/G]GTGCTTTGGAGGCCA	9972
rs566882123	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669184	CCCAAGTTCAAGTGA[C/T]TCTCCTGCCTCAGCC	9972
rs566883935	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17662949	AAACAAAAGGAACTG[C/T]TCTAGACTAAAGGAG	9972
rs566888138	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695144	AGCTTTAAATCTCAC[A/G]AAATTCCCTTTAAAT	9972
rs566905982	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703439	TCCAACTTTCTGCTA[C/T]ACTACCAAAAGCTTA	9972
rs566986746	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636681	CCATGTTTCTGGCTG[A/C]CTAGATTAGAATTAG	9972
rs567012522	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685212	AGCTTTCCAGAATCT[C/G]ACACTACTTCAACAG	9972
rs567028761	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17702696	AAAGAAAGGAGAAAA[A/G]AAAAATGACACCATT	9972
rs567034588	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696537	GAGGCGGGTGGATCA[A/C]AAGGTCAGGAGATCG	9972
rs567075796	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17647060	CCGTGCCCGGCCTCA[A/G]ATGCCATTTTCTAAT	9972
rs567131079	in-del	-/C	0.0049648	0.0495757	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707966	CTATAAATCTTTTTT[-/C]TTTCTTTCTTTCTTT	9972
rs567197241	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690783	GAGGCCTTAAAATAT[C/T]CTGCCAACAAAAAAA	9972
rs567202520	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624273	TTCAAAGCTAGCCTT[A/G]CAAGCCCAAAAATTC	9972
rs567218366	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708377	TGAGACGAAGTTTTT[A/T]CCTCTTGTTTTGCCC	9972
rs567236106	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657405	AAATAAAAAAATAAA[A/T]AAAAAAAAAATAGCT	9972
rs567293490	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651128	ACACAGCAAGACCCC[A/G]TCTCTATAAAAACTA	9972
rs567326398	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618763	AGTAGAGATGGGGTT[C/T]CACCGTGTTAGCCAG	9972
rs567380192	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683213	TTCTCCCCCAAATTA[A/G]CCTTGACTTGAAACT	9972
rs567390659	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17656361	TGACACAAAATTGGC[A/C]GTTGGCCAGAATGAA	9972
rs567411554	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17655157	AAACTCATGGATTGA[C/T]TGGTAGGACAGTAAA	9972
rs567441689	snp	C/G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682818	AGCTACTCGGGAGAC[C/G/T]GAGGCAGGAGAATTG	9972
rs567479842	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17629565	ATAAAAGACACCACA[C/T]AGACACTCAATGTAC	9972
rs567500361	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17619718	TCAGAAGAACTATTA[A/T]TGTTAAAATGGCCAT	9972
rs567509579	in-del	-/CACCTGGAGAAAAGATACCT	0.00318978	0.0398085	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632431	AGAAATTTTTTTTCC[-/CACCTGGAGAAAAGATACCT]CACTGTTGACAAGCA	9972
rs567510787	snp	C/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614860	GCACCAGGCAAGAAG[C/T]AGGGTACCTTCTATA	9972
rs567523727	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676072	TTTTTTGATGGTGTA[C/T]TTTGTAATACAGAAA	9972
rs567539407	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17645638	CGGTTCAGAAATTAT[A/G]TATCACAATCTACAT	9972
rs567548072	snp	A/C	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17631919	TTGCAGTGAGCAGAG[A/C]TCGGCCACTGCACTC	9972
rs567582104	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17673649	ACAAATCAAAATCAG[A/C]AGTTGGGGTTACCAC	9972
rs567608661	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625525	ACAGAGCAAGACTCC[A/G]TCTCGAAAGAAAACA	9972
rs567686113	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676612	ATAAGTGGGACCAGA[C/T]CAGTCCTTCTACTGT	9972
rs567693001	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655414	CTCTTCCAAAGGCCC[A/G]TGAAAATGCCGCCCC	9972
rs567708798	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632288	CCTGGGCAAAAGAAC[A/C]AAACTGTCTCAAAAA	9972
rs567745775	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17670408	TGACCCTGTTAAACT[C/T]GCTTATTAGTTGTGG	9972
rs567755875	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672523	TCTGGTTGCAGTGAG[C/T]CATGATCGTGCCACT	9972
rs567758295	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17648474	ATACAAAAATTAGCC[A/G]GGCATGGTGGTGCGC	9972
rs567766706	snp	A/G	0.000230772	0.0107393	synonymous-codon	NUP153	GRCh38.p7	6:17626007	GGCAGAGCTGCTCAC[A/G]GGATTGCTGGACTGT	9972
rs567781927	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17658533	GTTGACAATAACCAG[C/T]CACTGGAAGTTGACA	9972
rs567786886	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17640865	TGGCCTCAGGTGATC[C/G]TCCCACATCGGCCTC	9972
rs567830415	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17695835	TAACACGGTGAAACC[A/C]TGTCTCTACTAAAAA	9972
rs567848446	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641271	CCAGGCACGGGGGCC[C/T]GTGCCTGTAATCCCA	9972
rs567967055	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701610	AGGTTGCAGTGAGCC[A/G]AGGTCGCACCATTGC	9972
rs567993397	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17653172	ACGGGAGAGTTGCTT[C/G]AACTTGGGAGGTGGA	9972
rs568003591	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17670866	CCCAGGCTGGAGTGC[A/G]GTGGCACAATCTCGG	9972
rs568018830	in-del	-/TC			intron-variant	NUP153	GRCh38.p7	6:17622828	TCTAACCTTACAGTG[-/TC]TCTATATTAAGCAGA	9972
rs568029217	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707503	GGGAGCTTTAAAATC[C/T]ACCTTATAAAGCTGT	9972
rs568071334	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659804	TATAATTAATAAAGA[A/G]CTTTAATGACAAAAG	9972
rs568133453	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660583	ATATTTCTTAATATA[C/T]ATATAAGAAATTATA	9972
rs568154105	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17627248	ATCAAATCTGATTAG[A/G]CCCTATCATGTTTTT	9972
rs568321863	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619823	ACATATCCGGCCAGG[C/T]GCTGTGGCTCACACC	9972
rs568344421	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622132	TTTTTTGGACAGTTA[C/T]GCTGCTACCCAGAGT	9972
rs568344536	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694328	TTTCTGGTCCATTTA[C/T]GTACTGTTTTACAGA	9972
rs568381895	snp	A/C	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17687221	TAGGATAGAAAAGAT[A/C]ATTTCTACAGCTATC	9972
rs568406927	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700127	AAAATTCAGAGACAA[C/T]ATGAAGACCCTAAAT	9972
rs568428035	snp	A/C			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632300	AACAAAACTGTCTCA[A/C]AAACAAACAAACAAA	9972
rs568442204	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615650	GCACAAACTCAGCAT[A/G]GAAATCATCCGTTTC	9972
rs568479920	in-del	-/A	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17644052	CTGTGTTAGCCAATT[-/A]AAAAAAAAAGATAAG	9972
rs568486826	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17693728	CCAGCACTACTAAAA[A/G]TACAAAAATTAGCTG	9972
rs568506403	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679998	CTTGCGTACCCTACC[C/T]TGCAGGTGCTTTGCC	9972
rs568523304	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654602	TGCGATTACAGGCAT[G/T]AACCACCGCGCCCAG	9972
rs568547914	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699363	TAGCCAGGAATAATG[C/G]TGCGTGCTACTCCAG	9972
rs568590571	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648274	AGGGAATTGCTTGAA[C/T]GCAAGATTTCAAGAC	9972
rs568628522	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17617208	CACAACTTACCTATG[A/G]CCAAGGGGAAAAGGG	9972
rs568632447	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685381	AGAAACCCCGTCTTT[A/G]CTAAAAATACAAAAA	9972
rs568666675	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17663732	TAAATTGAGTTGTTA[A/G]AAATGAGATAAAATA	9972
rs568671364	in-del	-/AAAG			intron-variant	NUP153	GRCh38.p7	6:17686153	TCTTGTCTTTAAAAA[-/AAAG]AAAGAAAGAAAGAAA	9972
rs568690272	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617685	CTATCTCTATAAAAA[A/T]TTTTTCAAAATTAGC	9972
rs568701788	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17665846	TGCGCCACCACACCC[A/G]GCTAATTTTTTTGGT	9972
rs568705442	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17642952	TGATTCTACTTACAT[G/T]ACATATTCAGAATAA	9972
rs568743866	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17635083	CCACATGCAGCCCAC[A/G]GGTTGCACAGCTTGG	9972
rs568743922	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643011	GACAGTTAGCTAGGG[A/G]GAAGGCAGAATGGGG	9972
rs568751840	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618265	TAGAAAGGATTTAAG[C/T]GGTATTTACGTGTCC	9972
rs568791932	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17673608	CACATGAAAAGACAT[A/G]CAACATCATTAGTCA	9972
rs568817214	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17680645	AATGTAATCAACAGA[G/T]TAAAAGGTCAACCTA	9972
rs568818476	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630123	GTAAGAATATATAGG[A/G]GTATGTATGTTTGCC	9972
rs568832274	snp	C/T	1.65012e-05	0.00287234	missense	NUP153	GRCh38.p7	6:17629434	CCAAATTTAAAATTT[C/T]CAGTGCTTGTTAAAG	9972
rs568867251	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667490	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAAG	9972
rs568875600	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650592	CACAGCTCAATAAAA[C/T]TGATCCAAAAGCCCA	9972
rs568880047	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17651637	TAAGAAGGCTTATTC[C/T]AGTAAGAGTGGCTGT	9972
rs568889391	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622589	GTGTGACTCTAATTT[G/T]TAGGGCCTCTGTAGC	9972
rs568893774	snp	A/G	1.6473e-05	0.00286988	missense	NUP153	GRCh38.p7	6:17637326	GTCTCAGCACTTTCC[A/G]AAACCACTGTCAATG	9972
rs568982240	snp	A/G	0.000399281	0.0141238	missense	NUP153	GRCh38.p7	6:17637698	AAGCTACTTATTGCT[A/G]GTCTTGTATAAACTA	9972
rs568985885	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673045	AGAATACACACACAC[A/G]CACACACACACACAA	9972
rs569017310	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691943	GTAGCCAGGACTACA[A/G]GCCGACTACCACATC	9972
rs569032623	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17661962	TACATGTAAATTAAA[C/T]ACAGACCTTACAAGT	9972
rs569043659	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17637993	GATGTTTTGTTTACA[A/G]GATATCACCTTCTCC	9972
rs569045504	snp	A/G	0.0142736	0.0832652	intron-variant	NUP153	GRCh38.p7	6:17630750	AGAGGGGAGGGGAGA[A/G]GGGAGGGGAGAGGGG	9972
rs569061651	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694319	AAAGACCCTTTTCTG[A/G]TCCATTTATGTACTG	9972
rs569065052	snp	C/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17697531	TCTCCATTAAAAAAT[C/G]CAAAAATTAGCCAGG	9972
rs569078787	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698224	GGATAGGGTAAACTT[C/T]GCTGCTGAATGGCAT	9972
rs569094400	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17662651	AATACTTATTCATTA[C/T]GAAAGGTAAAATAGT	9972
rs569105875	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650190	GAGCAACCAAAAGCA[A/G]GAAGAAACTGGATGG	9972
rs569119412	snp	A/G	1.64827e-05	0.00287073	synonymous-codon	NUP153	GRCh38.p7	6:17649271	GGTGATCGGTAGAGA[A/G]ATTTTCGGTAATACT	9972
rs569155948	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656729	CGCAAATTGGCCTTA[A/G]GGTAGTATGTTTATT	9972
rs569171062	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17644244	AAACTCAGAAGATCA[C/T]TGAAGAAACGCTTTT	9972
rs569180376	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17643634	GCTCAAAAAGAGGGG[A/G]AAAGGAGACAATGGA	9972
rs569183085	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703400	CCATTAACTAACAGC[A/G]CCAGACCTCTCATTG	9972
rs569200139	snp	A/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17663584	TCAAAATATTTTTCA[A/G]AATTTTAATGTTAAC	9972
rs569234276	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706951	ATCGGCGCCCGACGC[-/A]TTTGCATCATCATGC	9972
rs569299530	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686021	GGCGTGGTAGCACAC[A/G]CCTATAGTCCCAACT	9972
rs569338016	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687842	AGGCTTGGCTGGGCA[C/T]GGTGGCTCACGCCTG	9972
rs569363367	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17678465	GTGAATTTTAAATTT[C/T]AGCAAATGTCTATTT	9972
rs569380346	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669228	GGACTACAGGTGTGC[A/G]CCACCACACCCGGCT	9972
rs569402140	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668787	GCCATAGGTCGCAGT[A/G]AGTCAAGATGGCACC	9972
rs569403545	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17624945	TTTCAGACTCTTACC[C/T]TGCTAACCAAATTCC	9972
rs569459073	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652518	CTATCTTTGTAGCCC[A/G]GGGATAGGCAAAATT	9972
rs569464685	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17666104	AGTGCTGGGATTACA[G/T]GCATGAGCCACTGCA	9972
rs569466270	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684554	GCAACTGGCTGCTTT[G/T]CTTTCATATTATCCT	9972
rs569473544	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17646695	ATAAAATAATGATGG[C/T]GTGTTCCTAATGCCC	9972
rs569475429	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17618015	AAGTGTAGCTCGATA[G/T]TCACAAAATACCGAG	9972
rs569486784	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708271	CCGTGTGAGCCGCCA[A/C]GCCCAGCCTATTTAC	9972
rs569589589	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690680	CAAAGAAAGAGTCAA[A/G]GAAAGGAAAAAAATG	9972
rs569590157	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615041	AGAACAAAAAGTATG[A/T]CATAATTTTTTATTG	9972
rs569592675	in-del	-/AAAAAAAAAAA	0.493432	0.0569306	intron-variant	NUP153	GRCh38.p7	6:17670096	GCGAGACTCTTTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAG	9972
rs569612812	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17696527	TTGAGAGGCCGAGGC[A/G]GGTGGATCACAAGGT	9972
rs569636007	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NUP153	GRCh38.p7	6:17651874	CAAGATGGGATGATC[A/G]CTTGAGCGCAGGAGC	9972
rs569649733	snp	C/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17689793	GCCTCCCAAAGTGCT[C/G]GGATTACAAGCATGA	9972
rs569661061	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702114	TCTCCAAAGAGCTGA[A/C]TTTCTGTGCCTGACA	9972
rs569674140	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702444	ACCCGGGAGGCAGAG[C/G]TTGCAGTGAGCAGAG	9972
rs569758833	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639325	CTCAAGTGATCTGCC[C/T]GTCTTGGCCTCCCAA	9972
rs569876949	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17639434	GAACATCCTGTTTTC[A/G]AACAAAAAATTATTC	9972
rs569889763	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	NUP153	GRCh38.p7	6:17614542	TTCGTGGGATATAAA[A/C]CCTGCACATTCGGAG	9972
rs569893704	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694822	TCTCTACTAAAAATA[A/G]AAAAAAAGTAGCCGG	9972
rs569943086	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17682766	TACTAAAAATACAAA[A/C]AATTAGCTGGGTGTG	9972
rs569946061	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702571	ATGCCAGCTACTCGG[C/G]AGGCTGAGGCAGGAG	9972
rs569981881	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664779	AGGTAGTGGCCAGGC[A/G]CGGTGGCTCACATCT	9972
rs570001541	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619809	CCATAGAAATAGAAA[C/T]ATATCCGGCCAGGCG	9972
rs570068941	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17683124	AAAGTTATCCATGGG[A/G]GCTGGAATCAACTTT	9972
rs570111401	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666441	AATCGTTTGAACCCG[A/G]AGGCAGAGCTTTCAA	9972
rs570111455	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690847	GTAATTTCCTTACTA[C/T]GTGAAAAGGTAGCCG	9972
rs570150085	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620387	TGACAAGAACACGCA[C/T]TGGGAAAAGGATACT	9972
rs570151970	snp	C/G	0.00358779	0.0422022	intron-variant	NUP153	GRCh38.p7	6:17695234	AGTCACTTATAAAAG[C/G]ACTAAAACAGTGGTT	9972
rs570175746	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634113	GTTCATGAACCCCCC[A/C]CATTACTCCCACCAC	9972
rs570187630	in-del	-/AAAC	0.0189856	0.0955633	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632301	ACAAAACTGTCTCAA[-/AAAC]AAACAAACAAACAAA	9972
rs570195709	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17694157	GAACATAAGCTCCAA[C/G]AAGGCAGGAACTTGT	9972
rs570211467	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679966	CTCAAGGTAATCATC[A/G]CAACCAGATATGCTG	9972
rs570230649	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17646696	TAAAATAATGATGGT[A/G]TGTTCCTAATGCCCA	9972
rs570249457	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17628019	ACTTGGATCACTCTT[C/T]GTACTGGTGCACTAA	9972
rs570253913	snp	C/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705062	GCGCCCGACCCAAAT[C/G]TTTACTTTTAAAAAT	9972
rs570278645	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17659718	CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	9972
rs570332967	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700381	ACTTGTCCAAGTCCA[C/G]GCAGAACAGGGATCC	9972
rs570342242	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653812	CTCTTGATAGGGCTT[C/G]CATTACACAGATGTA	9972
rs570366789	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647493	TATCATGTCAAATTT[C/G]TTGGGTATGATAGCT	9972
rs570393365	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706133	TCGCCACCCCCAACG[A/G]CCTGAGCTCCCCCGG	9972
rs570412120	snp	C/T	0.00993419	0.0697739	intron-variant	NUP153	GRCh38.p7	6:17692287	CCCAGAAGAGCTTAA[C/T]AGAGGAACAGTGAGA	9972
rs570412628	in-del	-/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17680651	ATCAACAGAGTAAAA[-/G]GTCAACCTACAGGAT	9972
rs570427845	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17641343	AGATGGAGACCATCC[C/T]GGCCAACATAGTGAA	9972
rs570468249	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17654612	GGCATGAACCACCGC[A/G]CCCAGCTGACCTTGA	9972
rs570529087	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655274	GGGTAATTTTACATA[C/T]AGAGTTCTATTAACC	9972
rs570565127	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671650	ATACCATGTTCATGG[C/T]TTGGAAGACTCAATT	9972
rs570607996	in-del	-/A	0.00835141	0.0640778	intron-variant	NUP153	GRCh38.p7	6:17642747	ACATATGTTCACAGC[-/A]AGCACTATTCACAAT	9972
rs570649954	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687128	CAAATATACATAAAC[C/T]GTACAGAGAATAAGA	9972
rs570655175	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666716	TAAGTACACCAACTG[C/T]TTTGTTAACAGTCCT	9972
rs570668987	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622498	TTTTCTAACATCTTT[A/C]CTATCCAGGTCTACC	9972
rs570694229	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17672518	GAGGTTCTGGTTGCA[A/G]TGAGCCATGATCGTG	9972
rs570717943	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17660662	GAAAACTCAAATGTC[C/T]AAAAAACACACAAAA	9972
rs570733161	snp	G/T	0.00517822	0.0506191	intron-variant	NUP153	GRCh38.p7	6:17616979	ATGGTCTCGATCTCC[G/T]GACCTTGTGATCTGT	9972
rs570840884	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692799	TCCCACCTGTTTTAT[A/C]AAGCCCTCTGAAGTG	9972
rs570960126	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17643497	CCCCACCAAAAATAA[A/C]CACCACTCGTACAAC	9972
rs570962714	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643201	ATATAGGCTGGACGC[A/G]GTGGCTCACACCTGT	9972
rs570979801	in-del	-/ACATCAG			intron-variant	NUP153	GRCh38.p7	6:17662835	TCTAATCATGAGGAA[-/ACATCAG]ACAATCATAAAACTG	9972
rs571019616	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17636605	AGTTAAAGATTCAAT[A/G]TGAATCTTCACTAAT	9972
rs571021348	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679906	CCTCAGGAAGGAATG[C/T]GAAATAACTGATTTA	9972
rs571023069	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691428	CTTATCCCATTTCCA[C/T]ACTTCAAGACTTGAA	9972
rs571023131	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698052	TTCAGATTATAAAAT[A/C]TCCTTTCTCAAATAG	9972
rs571028026	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635678	TGCTGGGATTACAGG[C/T]GTGAGCCACAGTGTC	9972
rs571081436	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677349	CTCTACACATTATCA[C/T]TCAAAATGCCAATAT	9972
rs571084431	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17697412	ATTAATGAGCTGGGC[A/G]CAGTGGCTCATGCCT	9972
rs571090976	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17660464	ATATAGACAGAAAGG[G/T]TAATGTAACCAATCT	9972
rs571170425	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17681859	AGGATAATTTTCTAA[C/T]TCTTGGCAGACATCA	9972
rs571182888	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17668637	CACCTGAGCTCAGGA[A/G]TTTGAGACCAGTCTA	9972
rs571187188	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668201	CTGCCTCAGCCTCCG[A/G]AGTAGCTGAGATTAC	9972
rs571279329	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618283	TATTTACGTGTCCTA[C/T]ACTCATAACAACTAC	9972
rs571306792	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17701532	CTGGGCGTGGTGGCA[C/T]GTGCCTGTAGTCCCA	9972
rs571372155	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631419	ATGGATATGTTGCCT[C/G]GCAGTGAAGTTTGGG	9972
rs571391697	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17637107	ATAAATTAAACTGTT[C/G]AACAGAAGTAATAAG	9972
rs571418068	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656806	GAAAAGTCCTTCGAC[A/G]TGCACAGTTGTCTCT	9972
rs571442314	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625065	CAATTAACAACTACT[C/G]CACACCTTTACAGCC	9972
rs571485367	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650234	GAAAATGGGAAGGGC[A/G]CTGAGTAAGCTTCCT	9972
rs571505713	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17625467	CTCGGGAGAGGCAGG[C/T]TGCAGTGAGCTGAGA	9972
rs571531690	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17656597	GCTCAGGCTAATCTC[A/T]AACTCCTGGGCTCAA	9972
rs571542547	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17650925	TTACAGGATGTGGTA[A/T]GAAAGTAACATAAAG	9972
rs571552497	snp	A/G	0.0023933	0.0345097	intron-variant	NUP153	GRCh38.p7	6:17638139	CTTTCTCCTTCATCC[A/G]TTTCTTCTTTTAAGT	9972
rs571587597	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17655276	GTAATTTTACATATA[A/G]AGTTCTATTAACCTG	9972
rs571661231	snp	A/C	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17645262	AAAAAAAAAAAAAAG[A/C]ATTCTATGTTTTAAT	9972
rs571738091	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17683809	GGTATCTTCTTCCAA[C/T]GGCGGGCCATGTTTC	9972
rs571775412	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664126	ATTCAGCCATAAAAA[C/G]GGAAAAAATGAAGTA	9972
rs571807861	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619069	CCACATCAAGACACA[C/T]CCTGATGTATCAGAA	9972
rs571843558	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17652608	TTAGAACATCTGCCA[A/G]TCAAAAGATATCATT	9972
rs571985615	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695933	AGAATGGCGTGAACC[C/T]GGAAGGCGGAGCTTG	9972
rs572026279	snp	G/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17631696	TCCAGACCAGGCGTG[G/T]TGGCTCACGCCTGTA	9972
rs572061382	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17657678	AAAGCTAACCTGTAT[C/T]TTCCTCATACAGAGA	9972
rs572074682	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17703318	CAAGTCAAATGAACA[C/T]ATGCAGAAGTCATAG	9972
rs572171810	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701305	GAGGCCGAGGAGGCC[A/C]GACCACGCAGTGAGG	9972
rs572171942	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694440	GACGCGGGCGGATTA[A/C]CTGAGGTCAAGAGTT	9972
rs572172771	snp	C/T	0.000422171	0.0145226	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706247	GAGTTTCCCCACCCG[C/T]CAGGCCACCGCGGCG	9972
rs572174302	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706772	CGCCCTAGCCGTAGC[C/T]GCCGCAGTTGAAGCC	9972
rs572181200	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17664378	GAGAATTGTATGATA[C/T]GTGAATTATCTCAAG	9972
rs572234904	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17700676	TCACAAAGAAGCTAC[C/T]AAAACAAATAAAAAC	9972
rs572278419	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625635	TGTTAAAGTTGAACA[C/T]AGAGAGTGTACATTA	9972
rs572342325	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619313	GCCTCAATGTTTTCC[A/T]TCCCTGAACCCTCAA	9972
rs572401571	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17633085	TATAAATGAGCAGCT[C/T]ATAATCACCTTGCTC	9972
rs572406478	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699049	AACTGAAATATCTAT[A/G]GATAGAAAAGGCATC	9972
rs572415765	in-del	-/A	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17659815	AAGAGCTTTAATGAC[-/A]AAAGAAAATTGGTTT	9972
rs572460945	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686560	GCCACCATGCCTGGC[C/T]AATTTTTTGTATTTT	9972
rs572468379	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666933	GCAAATGTGACCTTA[C/T]ATACAACTCAATAAG	9972
rs572524992	snp	C/T	0.00716266	0.059414	intron-variant	NUP153	GRCh38.p7	6:17682080	CTAGGCATGGCAGCA[C/T]GCTCTTGTAGTCCCA	9972
rs572535709	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703811	TAAAATATGTTTTCT[C/T]TTTTAATTAAATAGG	9972
rs572554743	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653376	TACAATGAGATACCA[C/T]CACACACAAACCAGA	9972
rs572617558	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17646777	GGAGTTTCACTCTTG[C/T]TGCCTGAGCTGGAGT	9972
rs572618653	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641082	CCTTGTATTTAGAGA[C/T]CTACATTTTCAGTGT	9972
rs572646051	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17677856	ATGGGATCCTTTCTT[A/C]TTTCGTGTTTTCTGA	9972
rs572693466	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634309	TCCCTGTAAGTTAGC[A/G]GACTTTCATTTCAGG	9972
rs572718406	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704587	ACTAAGCACTTTATG[C/T]ACATATCTGGGGGAA	9972
rs572761888	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686348	GATACTGACTTTATG[C/T]AGGGCTAGGTTAATG	9972
rs572776822	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17653143	CTGTAATCCCAGCCA[A/C]TTGGGAGGCTGACAC	9972
rs572785282	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648393	AGGCCAAGGCAGGCG[C/G]ATCACCTGAAGTCAG	9972
rs572787110	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671166	TAAACCCCACTTGAT[C/T]ATGATGCAGTTTCCT	9972
rs572848683	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642403	TCAATGGGTAAAGGA[C/T]GTGAAAGGCATTCCT	9972
rs572850299	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17665659	GACTTTTCACACACA[C/T]GCATGCATACAAAAT	9972
rs572850451	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17649022	TTTTTTAAAAAAGCA[A/C]AACAGCATTTCCATT	9972
rs572912821	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660770	ACATCTAATACAGCA[A/G]AAGATGTGGATCATC	9972
rs572927140	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17615916	GCTATTTATTTATTT[A/T]AAAAAGGGTGGGTGA	9972
rs572948261	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625307	TTTGAAAGGCCGAGG[C/T]GGGCAAATCATGAGG	9972
rs572948705	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17616462	ATGACTTTTAAAAAC[A/G]AAACATATACATGCA	9972
rs573068217	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17651190	ATGCCTGTAGTCCCA[A/G]TACCTGGGAGGCTGA	9972
rs573105885	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684947	AAAACAATTACAATA[C/G]TAATACCAAAGAGCA	9972
rs573137366	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668223	TGAGATTACAGGTGC[A/G]CACCGCCACACCTGG	9972
rs573144558	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17669765	AAATTACCTTTACAA[C/T]AACAAAAGAATGATA	9972
rs573172942	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692315	AGACAGAGACATTAC[C/T]AGTGGCACAGTGAAT	9972
rs573200241	snp	C/T	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17662157	ATTAATTTTAATATT[C/T]AGAATCAGGAATTTG	9972
rs573266227	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673230	AAAAATCAGCCAGGT[A/G]TGGTGGCAGGCACCT	9972
rs573288298	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17629765	GCCACTTTTCATTTA[C/T]CAGACTGGCTGCGAT	9972
rs573376171	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696860	GGCAGATCACTTGAG[A/G]TCAGGAGTTTGAGAC	9972
rs573384570	in-del	-/CACTG	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17701791	GAGCCAAGATTGTGC[-/CACTG]CACTGCACTCCAGCC	9972
rs573449425	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708639	CCACCGCGCCCAGCC[C/G]ACTGATCCTGTTTCT	9972
rs573468685	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622857	AGATAAAGGCTGGGC[A/G]TGGTGGCTCACACCT	9972
rs573477165	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655745	CAGGTGTGAGCCACC[A/G]TGACCAGCCAATCTT	9972
rs573505405	snp	A/C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621275	GTAAATTAGTATAAC[A/C/T]GTTATGGAAAACAGT	9972
rs573519278	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656436	AAGAGGAGTTTTTTT[A/T]ATTTGTTATTTTTTT	9972
rs573532258	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17617393	AAAGAACAGAAGCAA[C/T]TGCATTTACACCAAA	9972
rs573546582	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17623444	AACTCATACAATGGT[C/G]GTAGGATATGAATTG	9972
rs573595466	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701711	TGGTGGCCTGCGCCT[C/G]TAATCCCAGCTACTC	9972
rs573613083	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17617855	ATCTCAGAAGGAAAA[A/G]AAAAAAAAAGAAAAA	9972
rs573657421	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707661	CAATAAAAGTATACT[A/G]TATTTGCTCCAAATA	9972
rs573663633	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650391	TCAAAGTCTACATAT[A/G]AGCCACCCGAATCTC	9972
rs573688145	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17618658	GCAAGCTCCACCTCC[C/T]GAGTTCACGCCATTC	9972
rs573725352	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17637087	CTAAAACAAGGATTC[C/T]TAGAATAAATTAAAC	9972
rs573762906	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643899	GGAAACATTTTAATG[A/C]CTTTCCTCATAATAA	9972
rs573792253	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17682951	AAAAAAACACTTTCT[C/T]TGCGCATCCACAAGA	9972
rs573824828	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17644498	TTTGCAATTCTAAAG[C/T]GTGTCATGCTTTTTC	9972
rs573881456	snp	A/G	0	0	intron-variant	NUP153	GRCh38.p7	6:17682341	ATGTTGATGGCTACT[A/G]ACTGATCAGGGTGAT	9972
rs573887183	snp	C/T	1.64779e-05	0.00287031	synonymous-codon	NUP153	GRCh38.p7	6:17675301	AGTGTGCTGTGAGAG[C/T]GAGTGAGAACGTTCA	9972
rs573911623	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631520	ATCCCATCCTCTCAC[C/T]GTTCTAGGGGTCTAC	9972
rs573945203	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17681641	TAGAAATCTGCTGGT[A/G]TAGGTATTTAAACCA	9972
rs573969974	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671567	TAACAAAATATGTTC[A/G]AGATCTGTATGCTGA	9972
rs573970215	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625105	TGGTAAAGGAACATA[A/T]CTCAGAATAATCTCC	9972
rs573991721	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668883	AAACATGTTCCCTAA[C/T]GTCTAAACTAAATCC	9972
rs573999594	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17677734	AATTTTTTTTTTCCT[-/T]TTTTTTTTTTTTTTT	9972
rs574016739	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17693057	ATACATACAGTTCAT[-/A]AAATTATTTTCCTAG	9972
rs574045403	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17657653	CTATACAATGCATCA[G/T]CTGGCAAATAAAGCT	9972
rs574049191	in-del	-/ACA	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17621549	ATCTTGTCATTTACT[-/ACA]ACATCTATGGCACTG	9972
rs574054743	snp	A/G	1.64806e-05	0.00287054	missense	NUP153	GRCh38.p7	6:17669474	ACTGCAATATTCGCC[A/G]AGCTGTTGAACTGGT	9972
rs574102510	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640305	AAAAAAATATAAACT[A/T]TAATTATCGTCCAAT	9972
rs574113404	snp	A/G	0.00134758	0.0259224	missense, intron-variant	NUP153	GRCh38.p7	6:17651856	CTCAGCACTTTGAGA[A/G]GCCAAGATGGGATGA	9972
rs574113964	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17651620	CCTGAAACTACTAAG[C/G]ATAAGAAGGCTTATT	9972
rs574137407	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17624087	AATATAGGATTATAA[C/T]ACAATTTGATTAGTC	9972
rs574200690	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17652120	AGTTGGCAATTTTAA[A/C]CCCCATCTCTCAATA	9972
rs574326655	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17694429	TTCCGGAGGCCGACG[C/T]GGGCGGATTACCTGA	9972
rs574359415	snp	C/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17632106	GCCACAGCCTGTATC[C/G]CTTTTAATTTAGAGG	9972
rs574392600	snp	A/C	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17670182	ACACCATTCTGTTAA[A/C]CCCTTCGGTAATAAC	9972
rs574503858	snp	A/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17626260	AGAATTTTCCTACCC[A/T]AGAATTCGCTAGAAA	9972
rs574579212	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706196	GTCTGCTCCACGTGG[A/G]GCGCCGGGGCCTCGA	9972
rs574583075	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17699705	CCAGGCGTGGTGGCA[C/T]ACACCTGTAACCCCA	9972
rs574590355	in-del	-/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17670806	GGTAAATCCCATTAA[-/T]TTTTTTATTTTTTAT	9972
rs574677166	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620053	CAGTGAGCCAAGATT[A/G]CACCATTATACTCCA	9972
rs574736846	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17653489	ATAAAATGGCACACT[A/T]TAGAAAACAGTATGA	9972
rs574738181	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17620732	TAGTGTTAATGTATC[C/T]TGTGTTTGGCCGAAG	9972
rs574743701	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620868	AAAATAGACAAGAGG[A/G]ACTATATTAAACTGA	9972
rs574786815	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703680	AAAAAGGAGAGTATT[A/C]TTTTGAATATACCTG	9972
rs574798478	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17646977	GGTCAGGCTGGTCTC[A/G]AACTCTTGACCTCAA	9972
rs574805147	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17681005	ACAATAGCCAAGATA[C/T]GGAATTGACCTAAGT	9972
rs574806983	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639703	CCTACCTCTATTAAT[A/G]GAGAATCCATTTCCT	9972
rs574819833	in-del	-/AAAG	0.00859275	0.0649811	intron-variant	NUP153	GRCh38.p7	6:17686157	GTCTTTAAAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA	9972
rs574824736	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17647664	AGAATACATGATTGT[C/T]CAAAAGTTTTTTACA	9972
rs574851739	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17703089	TGTAATCCCAACTAC[C/T]TGGGAGGCTGAGGCA	9972
rs574857209	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17631600	GATGAAATATCTGTC[C/T]GAGTTGTTTCAAGAC	9972
rs574869455	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680230	GGAAACCAAAGAGCC[C/T]GTGGTCTGTAATACT	9972
rs574882499	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616036	AGCACAAAGTACAAT[C/G]CAGTATCTGAAAGCA	9972
rs574890278	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700959	AAGCAGTGGCTCATG[C/T]CTGTAATCCCAGCAC	9972
rs574932498	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686201	AACTGTAAACAGCCT[C/T]AGGTAAGTCCTTCTG	9972
rs574950095	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17692221	AATACATGAACTTAG[A/G]TTACAGACCGATTTT	9972
rs574973173	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641119	GGTTTTATCGTTATA[C/T]TTTTAAGGGGCGATT	9972
rs574997363	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685715	ACTCAGTGTTACCAG[C/T]CATGTAAAACTAGAG	9972
rs575010800	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17625081	CACACCTTTACAGCC[A/G]ACAATTTCTGGTAAA	9972
rs575013117	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17698492	GCCTGTAACCCCAGC[A/G]CTTTGGGAGGCCGAG	9972
rs575019119	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671869	AAAAATTAGTGGGGC[A/G]TGGTGGTGTGTGCCT	9972
rs575034295	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17641448	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA	9972
rs575036227	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	NUP153	GRCh38.p7	6:17633577	CATCACCAAGTGACA[A/G]CCTAAAACAAGTGTG	9972
rs575037122	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672450	GAATGGTGGCACACG[C/T]CTGTGGTCCCAGCTA	9972
rs575040531	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17640445	CTAATCAAAAAAAGT[A/T]ATTTTCAACTGAGCA	9972
rs575099225	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17666885	CAGGGCAAAGCCTCT[A/G]TATGGTTACTAACTC	9972
rs575111122	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17642670	TACCATCTGACCCAT[C/G]AATTCCATTCCTAGG	9972
rs575127878	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618990	AATAATTCAGGAAAA[C/T]TCCCCAAAATGGAAG	9972
rs575141339	snp	A/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17684180	ACCATGAGCCAAATA[A/G]GCCTCTTTTCTTTAT	9972
rs575182611	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690997	ACAAAAAAAAATTAG[C/T]CGGGTGTGGTGGTGT	9972
rs575193096	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17635989	TACATCAAGGGCTTT[C/G]TTTTTGTAGGTGAGC	9972
rs575217094	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17666286	ATGTGGGAGGCCGAA[A/G]CAGGTGGATCATTTG	9972
rs575227337	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638415	TCCAGCCTTACCCGC[C/T]AAAGAAAAAGAAATT	9972
rs575277755	snp	A/G	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17660300	TTGGTCAATGAGGGA[A/G]TCACTGGTGAAATTT	9972
rs575307952	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17630334	GGCAACAGAAAAACA[A/G]AAGAATTACAGAGTT	9972
rs575341772	snp	C/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17660956	ATAAATATATAAGCA[C/G]TGAAATTAAAAAACT	9972
rs575342445	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17670944	GCCTCCCGAGTAGCT[A/G]GGATTACAGGCACGT	9972
rs575343219	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17645880	CATTTAAGGAGCTAA[A/G]TATCTCTAAAGATAA	9972
rs575349248	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17648433	ATCAGCCTAACCAAC[A/G]TGGTGAAACCCTGTC	9972
rs575395286	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691464	TTAAAAGCTATAATA[C/T]AGTTTAAGACAGACT	9972
rs575397269	in-del	-/A	0.00159617	0.0282053	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632579	AAGCTGTTCTCAAAT[-/A]ACTTCATTTTTAAAT	9972
rs575422462	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17648369	CGCTTGTAATCCTAG[C/G]ACTTTGGGAGGCCAA	9972
rs575434124	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643251	GCCTAGGCGGCCAGA[A/T]CACCTGAGGTCAGGA	9972
rs575460524	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667055	AAACTTTTATGGATA[C/T]GATACTCAACCATTA	9972
rs575463928	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17656514	CTGGTAGCTGGGACC[A/G]CAGGCGCTAACCACC	9972
rs575469770	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17655524	AGTGGTACGATCTCA[A/G]CTCACTGCAACCTCC	9972
rs575564783	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696633	GGTGGTGGATGCCTG[C/T]AGTCCCAGCTCCTCG	9972
rs575572977	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673291	GAGAATTGCTTGAAC[A/C]CAGGAGGTGGAGGGT	9972
rs575585507	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17689085	TTAAAAAAAAAAAAT[A/G]CAGGAACTAAAACAA	9972
rs575605851	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17629791	GCGATAAAGTTTGAT[A/G]AAGTTTGTACTAGTG	9972
rs575630389	snp	A/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17702590	CTGAGGCAGGAGAAT[A/G]GCTTGAACCCAGGAG	9972
rs575643562	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702334	AACACGGTGAAACCC[C/T]GTCTCTGCTAAAAAT	9972
rs575653527	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668290	TCACCATGTTGTCCA[C/G]GCTGGTTTTGAACTC	9972
rs575656752	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17622882	ACACCTGTAATCCCA[A/G]CACTGTGGGAGGCCG	9972
rs575747124	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17674726	AGTGTGGTCCGAGAT[C/T]GTGCCACCGCACTCC	9972
rs575783630	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17624344	AGTCAGAGTAAAAAT[C/T]AACACTTTAAAATAC	9972
rs575810993	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17675467	AAGTCAGAAAAAAAA[A/C]CCATAAAATTTAATG	9972
rs575847493	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618505	ATAAAAAGGAAACAT[C/G]CAGAAAATAAAAAAG	9972
rs575882388	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17649875	TCTGCAGTTTCAGGT[A/G]TGACCTGGGATTCTT	9972
rs575887364	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707397	GTTTTGTTGCAGACA[C/T]ACGGGGCTGGAATTC	9972
rs575937905	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661262	GAGGTTGCACTGAGC[C/T]GAGACTGCGCCACTG	9972
rs575962584	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17644619	TGTTTCTGATTTTCC[C/T]AAACACTTAAAAGAA	9972
rs575995485	in-del	-/A	0.00398564	0.0444627	intron-variant	NUP153	GRCh38.p7	6:17692932	TCTTCAGTTATCTAG[-/A]AAAAAATATACATGT	9972
rs576025698	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17683465	ATCTCATTAGAGCTC[C/T]TGGGTGACCAAATGC	9972
rs576090407	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17659007	GATGCACCAAAAACT[A/G]CAATGTCTGCAGCTG	9972
rs576094934	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695589	CCGACCTTCGAGTTG[A/G]TTTCCACCGTTAAAG	9972
rs576128368	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17695035	AACGAACAAAAAGGT[A/G]CTAAGACCCAAATAC	9972
rs576152250	snp	C/T	0.00159617	0.0282053	intron-variant	NUP153	GRCh38.p7	6:17689255	AGCAGGGCATGGTGG[C/T]GCATGCCTATAATCC	9972
rs576189964	snp	C/G	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17701388	CAAAAATTAGGCCGA[C/G]TGTGGTAGCTCACAC	9972
rs576209941	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17687574	TAAAAACCATTCTTT[C/G]AGGGCCATTTCATTA	9972
rs576232098	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17625205	TGTTTAATAAAACAA[A/C]TTCCAGTGTCTGGTT	9972
rs576243393	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631104	TCAAACTGCTAGTTG[C/T]ATACCATTAATCATC	9972
rs576256077	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633464	TATTAAGCATCATAA[C/T]ATACTTGGGTTCTGG	9972
rs576290088	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17669988	CAGTCCCAGCTACTC[A/G]AGAGGCTGAGGCAGG	9972
rs576305037	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17631612	GTCTGAGTTGTTTCA[A/G]GACATTAATCCTCAC	9972
rs576312247	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17625579	AAATTAAGTATTACA[C/T]TCTTACCACAATTAG	9972
rs576373831	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17619246	ACATCTATATTCAAT[C/G]AAAATCTTACCAAAC	9972
rs576437926	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643413	GGAGACGGAGGTTGC[A/G]GTGAGCTGAGATTGT	9972
rs576476444	snp	A/G	0.00318978	0.0398085	intron-variant	NUP153	GRCh38.p7	6:17660306	AATGAGGGAGTCACT[A/G]GTGAAATTTTAATTA	9972
rs576476659	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17681560	GTACTCCAGCCTGGG[C/T]GACAGAGCCAAGAAC	9972
rs576501842	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686275	CTCCATGGATGTTAA[C/T]GCCCCTGAAGAGTAT	9972
rs576549593	in-del	-/A	0.00159776	0.0282193	intron-variant	NUP153	GRCh38.p7	6:17679218	TACAAAAATCAACAC[-/A]AAAAAAATGTGTTTC	9972
rs576566857	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17655809	ACTGAAGAAAGAAAC[A/C]ATTTGTGGTCTCAAC	9972
rs576592462	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17659423	TTACTTTTGTACCAA[C/T]CTAATAAATTCCTTA	9972
rs576599840	snp	A/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17652283	CAGACCATACAGTGA[A/T]CTATAAAACAAGTCT	9972
rs576623975	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674702	TTGAAACCAGGAGAC[A/G]GAGGTTGCAGTGTGG	9972
rs576651780	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17640403	ATCCACTGCATGAAA[C/T]ATCTGATTACACAAC	9972
rs576653269	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17660117	TAGCTAGGAAAAGCA[C/T]AGTTAAAAGGAAGCA	9972
rs576661790	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17652890	AAAAATTAGCTGGGC[A/G]TGGTGGCGCACACCT	9972
rs576730741	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17699639	GTCAGAAGTTTGAGA[C/T]CACCACACCAACATG	9972
rs576757178	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643643	GAGGGGAAAAGGAGA[C/G]AATGGAAAACTTAGC	9972
rs576792532	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705310	CCTATTCAATACTTC[G/T]AACAATCAATATTTT	9972
rs576805769	snp	C/T	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17699153	TCTTTTAAAAATATA[C/T]TACAACCATGAAGAT	9972
rs576811895	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671113	CTGGTCTAATCCCAT[C/T]AATTTTCATATGTTG	9972
rs576822460	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17676995	AAAAAAACAATGCTG[A/G]GGACTCTCAAGTTTT	9972
rs576839354	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17648367	CACGCTTGTAATCCT[A/G]GCACTTTGGGAGGCC	9972
rs576870168	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704880	TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG	9972
rs576908735	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17620796	AAAAGATAGGACCCC[C/G]CTGGCCTAGGCAAAG	9972
rs576955728	snp	C/G	0.00119737	0.0244387	intron-variant	NUP153	GRCh38.p7	6:17625302	AGCACTTTGAAAGGC[C/G]GAGGCGGGCAAATCA	9972
rs576963490	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17621583	AGGACATTATGTTAG[A/G]TGAAATAAGCCAGGC	9972
rs576965021	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NUP153	GRCh38.p7	6:17614836	TATGCAAATTAGGCA[C/T]GATTCCTAGCACCAG	9972
rs576998701	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17672599	ACACAGAACAAAGAC[A/G]GTGCAAAAGCTATTC	9972
rs577018070	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17680136	ACCTCCACTGTTTCC[C/T]TTGCGCTCAAGCACA	9972
rs577060721	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17673139	TTTGGGAGGCCAACG[C/T]GGGTGAATCACAAGG	9972
rs577084098	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17679660	GTGGCACTGGTGAGA[A/G]AGAACAGGAGGTGGG	9972
rs577094404	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685973	AACAGAGTTTGACCT[C/T]GTCTCCACAAAAAAA	9972
rs577141605	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17702750	GGTAAAGGGGTAGGG[A/G]AGAAGGCAAGTAAGA	9972
rs577148314	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17685624	AAAATCTGTATTCCC[C/T]AGTGACATCATAGCC	9972
rs577219283	in-del	-/TCACGCCTGTAATACCAGCACTTTTGGGAGGCTGTGGCGGGTGGA	0.132158	0.220484	intron-variant	NUP153	GRCh38.p7	6:17702933	GCCGGGCGCGGTGGC[lengthTooLong]TCACGCCTGTAATAC	9972
rs577227860	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17686085	CCTGGAAGGTTGAGG[A/T]TGCAGTGAGCCATGA	9972
rs577331340	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17703595	ATAAACAGCAAGTGG[A/G]TAGACCCTATGTCCA	9972
rs577360852	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642448	AATGGACAATAAGCA[C/T]CTGAAAAAAATGCAA	9972
rs577389724	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692922	GAAAGGCTTAATCTT[C/T]AGTTATCTAGAAAAA	9972
rs577390410	snp	G/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17634762	CATCTGAATGTTGAC[G/T]TCAGCAGCTTGAAAT	9972
rs577400540	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17637980	AAATTCTACAAAAGA[C/T]GTTTTGTTTACAGGA	9972
rs577405810	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17667056	AACTTTTATGGATAC[A/G]ATACTCAACCATTAG	9972
rs577419347	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17691607	CCGTATCTACTAAAA[A/T]TACAAAAATTAGCCA	9972
rs577429724	snp	A/G	0.00279162	0.0372561	intron-variant	NUP153	GRCh38.p7	6:17658345	AGGCTGCAGTGAGCT[A/G]AGATCATGCTACTGC	9972
rs577439670	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17622357	GTAGTCCCAGTTTCT[C/T]GGCAGGCTCAGGCAG	9972
rs577457395	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17690008	GATAAGACAAACAAT[A/G]AAGTTAAATAACTTG	9972
rs577457793	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17696572	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	9972
rs577468468	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17661192	GGTGGCAAATGCCTA[C/T]AGTCCCAGCTACTTG	9972
rs577469080	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17667642	TTGCTTGAGCCCTGG[A/G]GGTGGAGGTTGCAGT	9972
rs577514074	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658699	GGTGTCTCACAAGCT[A/G]AGTGAAAATTTAAAA	9972
rs577556110	snp	G/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17678595	AAGTATTTTGTGATG[G/T]GCTGCTAGACTGTAT	9972
rs577577640	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17629657	AAGGGCCTACTTTGA[A/C]GAGTATTACCAGCAG	9972
rs577585551	snp	A/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17679533	TAAAATTCATATGGA[A/T]TCTCAAGGAACCTCA	9972
rs577594627	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620955	AAAAAGTTTGCTAAC[C/T]ATTCATCCAACAGGG	9972
rs577682486	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17684125	GAGACCACACTAAAA[A/G]CCAAGCAGATGCTGG	9972
rs577687994	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17671895	TGCCTGTAGTCCCAG[A/C]TACTTGGGAGGCTGA	9972
rs577690079	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17697637	AGGTTGCAGTGAGCC[C/G]AGATCACATCACTGC	9972
rs577723564	snp	A/C	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643280	GAGTTCAAGACCAGC[A/C]TGGCAACATGACGAA	9972
rs577780770	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17643765	ACACAACTCTAAATA[A/G]GCCACTCATAATCGA	9972
rs577800626	snp	C/T	0	0	intron-variant	NUP153	GRCh38.p7	6:17656363	ACACAAAATTGGCAG[C/T]TGGCCAGAATGAAGA	9972
rs577801464	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695013	GAGTGGGAAGTACTA[C/T]GGACTGAACGAACAA	9972
rs577806318	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17648956	TTCTCTATGGTATTG[C/T]ATAAGAGTTGAGGAA	9972
rs577813608	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17675154	AAGACTCTTGTCTCA[-/G]GAAAAAAAAAAAAAA	9972
rs577837916	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17636958	TATATACCAGACTAG[C/T]TAACACATAACCTAT	9972
rs577844563	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17650644	AGATAAAACAAAGAA[A/T]CTACTTCTATAAAAC	9972
rs577859597	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700923	GATAAAGAGGTTTCC[C/T]TCCCCTTTTTAAAAA	9972
rs577908189	snp	A/G	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17651511	CACAGAAAATGGACA[A/G]AAAGGCAAAACTCAG	9972
rs577938204	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17702234	CATTTCTGGCCGGGC[A/G]AGGTAGCTCATGCCT	9972
rs577965393	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17704031	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	9972
rs577967700	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17654120	TCTTTCAACATTTCA[C/T]GTTTGAAATTTGTCA	9972
rs577982428	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17701757	AGAGCTGCTTGAACT[C/T]GGGAGGCAGAAGTTG	9972
rs577990960	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708411	CTGGAGTGCAATGGC[A/G]CAATCTCAGCAACCT	9972
rs578007588	snp	A/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674213	TAACGTTTTGGGGTG[A/T]TGAAAATGTCTGATC	9972
rs578025221	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707946	TTGTGAAAAATCTTA[G/T]ACTTACTATAAATCT	9972
rs578034465	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17663040	GTGACAACATGTAAA[C/T]AGAATCTGTAGATTA	9972
rs578042589	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17652178	CCCCATGAAAAATGA[A/G]TAAGAACAAAGATCT	9972
rs578052522	snp	C/T	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17668446	TCAAGATCCTCAAGA[C/T]GGAAATGCTGAATAG	9972
rs578052639	snp	A/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17674631	AAAAATTAGCTGGGC[A/G]TGGTGGCATGTGCCT	9972
rs578063642	snp	C/G	0.000399281	0.0141238	intron-variant	NUP153	GRCh38.p7	6:17618600	AGATGGAGTCTGGCT[C/G]TGTTGCCCAGGCTGG	9972
rs578096760	snp	C/T	0.000798403	0.0199641	intron-variant	NUP153	GRCh38.p7	6:17663644	ATGACAAAATGTTAA[C/T]GACTGGTGAATCAAC	9972
rs578122559	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17618781	CCGTGTTAGCCAGGA[C/T]GGTCTCGATATCCTG	9972
rs578198543	snp	C/T	0.00199481	0.0315187	intron-variant	NUP153	GRCh38.p7	6:17682488	TGATAGCATTCTAAC[C/T]GCAGAATTTTCAAAA	9972
rs745319291	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17623187	CCTGTGTGAAAGAAA[C/T]AGAAACTTTCCAATT	9972
rs745331373	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636257	CAAGAATTGCATGCA[C/T]CTGGGAGATGGAGGT	9972
rs745333723	snp	G/T	3.31356e-05	0.00407022	intron-variant	NUP153	GRCh38.p7	6:17669347	TGCATCCTGTTAAAG[G/T]TGAAAAAATAACAAA	9972
rs745336507	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702323	ACATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	9972
rs745351534	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17689281	AATCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA	9972
rs745361832	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674741	TGTGCCACCGCACTC[C/T]AGCCTGGGCGACAGA	9972
rs745371563	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17635427	CATTATTTGAGACAG[A/G]GTCTCACTCTGTCAC	9972
rs745390612	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692116	CTCCACCCTCACTCA[C/T]AGATCCCTCATGTGG	9972
rs745404592	snp	G/T	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17628861	AAAACTAGGGAAGTA[G/T]AAGTGACAGGCTCTT	9972
rs745407357	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17643050	TTTAATGGACAGGGG[-/T]TTCCTGGTGAGGGTG	9972
rs745414299	snp	A/G/T	3.54354e-05	0.00420912	intron-variant	NUP153	GRCh38.p7	6:17637118	TGTTCAACAGAAGTA[A/G/T]TAAGCAAAATTACTC	9972
rs745446588	snp	C/G	4.9436e-05	0.00497148	missense	NUP153	GRCh38.p7	6:17625906	AATGGGGTGACAGCT[C/G]TACCTGTGCTGGATG	9972
rs745467678	in-del	-/A	1.9199e-05	0.00309825	intron-variant	NUP153	GRCh38.p7	6:17646164	CCAATCTGTAAAGAG[-/A]AAAGAATATCCTTAT	9972
rs745470473	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666778	TGGTATAAAACCACT[A/G]TAAAGCCAGAAGCTT	9972
rs745547716	snp	C/T	0.000164883	0.00907824	missense	NUP153	GRCh38.p7	6:17688407	TTACCTTCTGTATTA[C/T]TGACTGCTGGCTCAG	9972
rs745570393	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634400	TAATGACCCCAAATC[C/T]GTATCTCCACCCAAA	9972
rs745571714	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17673959	AGTGTCTTTTCACTG[C/G]TGAATAATAAACCAA	9972
rs745583008	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17685755	TTATGTACTCTATAG[A/T]ATACTATACTTGGTA	9972
rs745587447	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17640070	ACATGATGAGCTGTA[A/G]TTTTTTTAAATTTAA	9972
rs745589556	in-del	-/A	3.84408e-05	0.00438394	splice-acceptor-variant, intron-variant	NUP153	GRCh38.p7	6:17669030	TCCTATCAAGAGGCT[-/A]GAAAAAAAAAAAAAA	9972
rs745604293	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17629698	AATCCAAGGTGACCT[A/G]TATTTAGTCGGTATG	9972
rs745616597	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681845	AGGAGAAAAGTGATA[A/G]GATAATTTTCTAACT	9972
rs745618777	snp	C/T	1.66073e-05	0.00288156	missense	NUP153	GRCh38.p7	6:17629291	CTTTTTTAACTTCTT[C/T]GGGCTTAGATTCAGA	9972
rs745625358	snp	C/T	1.65803e-05	0.00287922	intron-variant	NUP153	GRCh38.p7	6:17675050	TGCACAGAAACAGAA[C/T]GATAAATTATAAGCC	9972
rs745672758	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17646471	TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG	9972
rs745681103	snp	A/G	3.3461e-05	0.00409016	intron-variant	NUP153	GRCh38.p7	6:17625802	TTTTTTCTTTTGTAA[A/G]TGTACCTGCAGAGCT	9972
rs745696892	snp	C/T	1.6483e-05	0.00287076	intron-variant	NUP153	GRCh38.p7	6:17662103	ACATATTTACGTTTG[C/T]TTATTTGTTGTAATT	9972
rs745704690	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17646263	CCCAGGCTGGAGTGC[A/C]GTGGCGCAATCCTGG	9972
rs745707765	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642320	AATATCTGCAAATCA[C/T]GTATCTGGTAAGGGT	9972
rs745838064	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17624962	GCTAACCAAATTCCA[C/T]CAAGACAAGTTTTAA	9972
rs745853761	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17692896	ACAGATGAATAAAAT[G/T]GTGCATTCTTGAAAG	9972
rs745853844	snp	A/G/T	3.29469e-05	0.00405864	missense	NUP153	GRCh38.p7	6:17637461	CCTATCACTGGTTTA[A/G/T]ATTTGTCTCCAAAGC	9972
rs745872601	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680388	TTAAATGGTTTTGGA[A/G]AACTGGATATCCACA	9972
rs745880567	snp	C/T	1.65105e-05	0.00287315	synonymous-codon	NUP153	GRCh38.p7	6:17629160	GGAAGATTTGGGCAG[C/T]TCCTCTTTCTTTTCT	9972
rs745900299	snp	C/T	3.3389e-05	0.00408575	intron-variant	NUP153	GRCh38.p7	6:17647946	GATACAAAAAGAGCT[C/T]TTTAGAAAAATAAAG	9972
rs745904947	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690702	AAAAAAATGACTCAG[C/T]AGGTACAGAAAACAA	9972
rs745933108	snp	C/G	1.64844e-05	0.00287087	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616085	AAATTGAGTACAACA[C/G]CAATGTGACCTTTAT	9972
rs745934160	snp	A/C/G			intron-variant	NUP153	GRCh38.p7	6:17650187	CAAGAGCAACCAAAA[A/C/G]CAAGAAGAAACTGGA	9972
rs745934783	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17663532	GCCTCTCAAAGCACT[A/G]GGATTATAGGCATGA	9972
rs745954125	snp	C/T	8.26235e-05	0.00642689	missense	NUP153	GRCh38.p7	6:17649165	AATGGTTTTGTACCT[C/T]GTTTGTTAATGCTTG	9972
rs745956744	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679396	TGGAAAAATATCCCA[C/T]GTACATGGACTACAA	9972
rs745957708	snp	A/G	3.32176e-05	0.00407526	missense	NUP153	GRCh38.p7	6:17628726	GATTCCTTCTCAGAT[A/G]GTTTTGTCATACTAA	9972
rs745965862	snp	C/G/T	3.29453e-05	0.00405854	missense	NUP153	GRCh38.p7	6:17637365	CGCTTCACACAAGTT[C/G/T]CAGGTTTCGGTGTTT	9972
rs745987579	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639012	ACATCTGGTGGGTAC[A/G]TTTAAATTCTTTCTG	9972
rs746037356	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17660331	TAATTAGAAACAAAT[A/G]ACAAATACAAGGACT	9972
rs746068517	snp	A/T	1.71249e-05	0.00292612	intron-variant	NUP153	GRCh38.p7	6:17665418	ATCAAAAACATTTAT[A/T]TTCATATAAATCAAT	9972
rs746075955	snp	A/G			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615436	CAAAATTGTATTTAC[A/G]CAAGTTTCATAATAA	9972
rs746128593	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620845	CAAAAGCACAGGCAA[C/T]AAAAACAAAAATAGA	9972
rs746130415	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	NUP153	GRCh38.p7	6:17647819	TACAGATGATGGAGG[C/T]AGTACATTTGCCTCA	9972
rs746154856	snp	C/T	1.75631e-05	0.00296332	missense, intron-variant	NUP153	GRCh38.p7	6:17669007	GAAAATCTGTGATAT[C/T]TATCCCACTCCTATC	9972
rs746160903	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17689361	CATGGCACTCTAGCC[C/T]GGGCAACAAGGGCAA	9972
rs746185305	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17617765	TGGGAAGATCTTCTG[A/C]GCCTAGGAGGTCGAG	9972
rs746201603	snp	C/T	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17675672	GCTGACAGTGTAATG[C/T]AGGGGATTCCAACAT	9972
rs746204257	in-del	-/TTTTT			intron-variant	NUP153	GRCh38.p7	6:17635114	CTTATCTTTTTTTTT[-/TTTTT]TTTTTTTTTGAGACG	9972
rs746204883	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17653971	GGGGGTGAAGTGTAC[C/T]AATGTCTTCAACTAT	9972
rs746217374	snp	C/G	3.4107e-05	0.00412945	missense	NUP153	GRCh38.p7	6:17629518	GCTGCTGAGTTCGAA[C/G]ATGAGGAAGATGTGT	9972
rs746243408	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17618928	GTATGACACAAAGAC[A/T]AAAGGTAAGAAGGAA	9972
rs746267642	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17621343	TTATGATCCAGCAAT[-/C]CCACTACTGGCTATT	9972
rs746279177	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644699	TGTAATCCCAATACT[C/T]TGGGAGGCCAAGGTG	9972
rs746306181	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666997	TGTGAAACATGGGCT[A/G]TGATACTGTATTCTG	9972
rs746316376	snp	A/G	3.29478e-05	0.00405867	missense	NUP153	GRCh38.p7	6:17624662	CCAAAAGTAGGTGGT[A/G]CAGGCTGAGAACCAG	9972
rs746323553	in-del	-/TAGAAT	8.27328e-05	0.00643114	cds-indel	NUP153	GRCh38.p7	6:17624561	TCACAGCACACTTAC[-/TAGAAT]TAGGAGTTGTTCCAG	9972
rs746357885	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707400	TTGTTGCAGACACAC[C/G]GGGCTGGAATTCTGG	9972
rs746379671	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628099	TCCTGCTATTCAGCT[C/T]ACAGAATGACTTTAA	9972
rs746424371	snp	A/C	1.6476e-05	0.00287014	synonymous-codon	NUP153	GRCh38.p7	6:17661731	ACCACCTACTCCAGA[A/C]GATAAACCATTGGCT	9972
rs746440619	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708672	GCTTCGTTTTTTTCA[C/T]CAGCAAATAGAGCGA	9972
rs746446124	snp	C/T	1.65847e-05	0.0028796	missense	NUP153	GRCh38.p7	6:17637726	CTACTGGGCTTGTTG[C/T]GGTGGGCTGAGCAGC	9972
rs746471079	snp	A/C	1.66247e-05	0.00288307	intron-variant	NUP153	GRCh38.p7	6:17675803	AATATTATGAATATA[A/C]AACTTAGAGCGATAC	9972
rs746471803	snp	A/T	1.65075e-05	0.00287289	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639961	TTTCAGAATATCTAG[A/T]ACACTTCCTTCTTTC	9972
rs746501123	snp	A/C/T	3.40961e-05	0.00412881	intron-variant	NUP153	GRCh38.p7	6:17625787	TCCAATTACAATGCA[A/C/T]TTTTTCTTTTGTAAA	9972
rs746505103	snp	C/T	8.23689e-05	0.00641698	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632753	ACAGTCCCAGCTTCC[C/T]TCGGGTTTCTTGAAC	9972
rs746511591	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644528	CTCTTGTTCCTGTGC[C/T]CTTGAGCTTTGTGTT	9972
rs746526923	snp	A/T	1.66161e-05	0.00288232	missense, intron-variant	NUP153	GRCh38.p7	6:17640061	ACTGTAGTGACATGA[A/T]GAGCTGTAATTTTTT	9972
rs746541592	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17660732	GTTGAACTGCAAAAC[A/T]ATCTTGAAGAGAAAA	9972
rs746543527	in-del	-/T	0.000117687	0.00767004	intron-variant	NUP153	GRCh38.p7	6:17640071	CATGATGAGCTGTAA[-/T]TTTTTTAAATTTAAT	9972
rs746587687	snp	A/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707853	ACACTGAGATGGGTA[A/T]TCAAAGCCAGGACTA	9972
rs746599162	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17657971	GAAATGATGTTAGAC[-/AA]AAGACAAGTTCGAGC	9972
rs746601555	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643714	GCTTTTTTAAATGAT[A/G]GAAGTGGTGAGAACC	9972
rs746618552	snp	C/G	1.72997e-05	0.00294101	missense	NUP153	GRCh38.p7	6:17624794	AATGCTGGACTGGCA[C/G]ATGGTGCTGAGGGTC	9972
rs746647834	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17617706	CAAAATTAGCCAGGC[A/G]TAGTGGCGTGCACCT	9972
rs746653084	snp	C/G	1.64844e-05	0.00287087	missense	NUP153	GRCh38.p7	6:17675012	GCTGACTGGTTTTAA[C/G]GATTGAAGAATTCCC	9972
rs746701549	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17684026	TGTTAAAATAGTCTG[A/G]GACCTCCTTACTCTT	9972
rs746711140	in-del	-/CTCA			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632449	CTGGAGAAAAGATAC[-/CTCA]CTGTTGACAAGCAAC	9972
rs746733378	snp	A/G/T	3.29724e-05	0.00406021	intron-variant	NUP153	GRCh38.p7	6:17662001	AAGAAGTATAGCTGT[A/G/T]TAAGAAATGACAGTA	9972
rs746738013	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691946	GCCAGGACTACAGGC[C/T]GACTACCACATCCAG	9972
rs746775504	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	NUP153	GRCh38.p7	6:17629079	CTTGTTCTCAGAGGT[C/T]ACTATGGTGTTAGCA	9972
rs746788963	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17662820	AGTAGGTAACTGAAA[C/T]CTAATCATGAGGAAA	9972
rs746806196	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688995	AAACAATACTTTCAA[C/T]AGCTTTCTCAAGCAA	9972
rs746817835	in-del	-/CATTATT			intron-variant	NUP153	GRCh38.p7	6:17663981	AAATGTTGACAGGAG[-/CATTATT]CATTACAGCCAAAAA	9972
rs746817982	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17640545	CCTATATGGTAAAAT[A/T]TTAAATAAGGGTATA	9972
rs746818206	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17680305	CCAGAAATAAACTAC[C/T]ATATATGATCAAACG	9972
rs746845976	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17652857	GGTGAAACCCATCTC[A/T]ACTAAAAATACAAAA	9972
rs746878590	snp	C/T			synonymous-codon	NUP153	GRCh38.p7	6:17661659	CAACCCTACCTCCTC[C/T]TCCAGAGGTTTAGAA	9972
rs746962560	snp	C/T	1.64893e-05	0.0028713	missense	NUP153	GRCh38.p7	6:17688600	TCTTAACAGATTCTG[C/T]AACCCTGCTAAGAAT	9972
rs746985560	snp	C/G	1.64966e-05	0.00287194	missense	NUP153	GRCh38.p7	6:17647902	TCGGAGAGGTCATTT[C/G]TACCTGGTTTTCCAA	9972
rs746999600	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620578	CCAGGACATTGGTCT[A/G]AGCCAAGCTTGTCCA	9972
rs747008403	snp	A/C	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637253	GGGCCTTTTGAATTT[A/C]TCTCCAAATCCTAAG	9972
rs747013724	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690879	GCGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	9972
rs747019985	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17620308	GACACATAGACCAAT[-/G]GAATAGAATAGAGAA	9972
rs747036472	in-del	-/TTT			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708346	GATCCTGTTTCTTTC[-/TTT]TTTTTTTTTTTTTTT	9972
rs747046170	snp	A/C	0.000152015	0.00871692	intron-variant	NUP153	GRCh38.p7	6:17665405	CAGGTAAAGAGAAAT[A/C]AAAAACATTTATTTT	9972
rs747062298	snp	C/T	1.65097e-05	0.00287308	missense	NUP153	GRCh38.p7	6:17626081	AACTACCAAATATGC[C/T]ACCACCAGCAGAAGT	9972
rs747081073	snp	A/C	3.5478e-05	0.00421162	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632602	TTTTAAATGGCCTTA[A/C]AAAAAGGCGCTTTAC	9972
rs747089578	in-del	-/CTC	1.64749e-05	0.00287005	cds-indel	NUP153	GRCh38.p7	6:17688454	AGTAATATTAGAGCT[-/CTC]CTCATCGGCATATAC	9972
rs747094022	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648747	GATGGAAGCTGCAAT[A/G]AGCTGTGATTGCACC	9972
rs747096744	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17681926	AGAAATCCAACACAG[G/T]CCAGGTGTGGTGGCT	9972
rs747101129	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17676691	AGTGGAAAACAGCAC[A/C]AAAAAAAACTCACAA	9972
rs747108604	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627411	TTCCAATTTATTATT[C/T]AAAAGTATTCATGGA	9972
rs747117475	snp	A/T	1.77919e-05	0.00298255	intron-variant	NUP153	GRCh38.p7	6:17626193	ATTAAGAAACAAACA[A/T]AAATCCTTAAGAATA	9972
rs747124203	snp	C/G	1.64846e-05	0.0028709	intron-variant	NUP153	GRCh38.p7	6:17647794	TATATACTATTCCTT[C/G]CTTGTTACTTACAGA	9972
rs747158463	in-del	-/TCT			intron-variant	NUP153	GRCh38.p7	6:17626352	AGTCAAATACATTCA[-/TCT]TCTTTTATAGCTTAT	9972
rs747159746	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17671399	TTTCTTTCTTAAATG[A/T]TTGGTAGGATTCACC	9972
rs747201274	snp	C/T	6.59565e-05	0.00574229	missense	NUP153	GRCh38.p7	6:17675564	CACTGGTAGTTGAGA[C/T]GTTATCATCATCATG	9972
rs747241785	in-del	-/CTT			intron-variant	NUP153	GRCh38.p7	6:17689536	ATTTTATTACGGTAA[-/CTT]CTTTTTTTTTTTTTT	9972
rs747246772	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619408	AAACGGGTTCCTCTA[C/T]GAAGCTAAAAGGAAT	9972
rs747255101	snp	C/T	4.94515e-05	0.00497225	synonymous-codon	NUP153	GRCh38.p7	6:17665299	AGAAGGAGTCAGAGA[C/T]GGTTTAAAATAAACA	9972
rs747272532	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17659864	TTTATATACTGTTTG[A/T]ATGATCAATGGCATT	9972
rs747290800	snp	A/G	4.94336e-05	0.00497135	missense	NUP153	GRCh38.p7	6:17675644	CCAATTGGGAATGCC[A/G]AGGATGTAGATGGCT	9972
rs747297782	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17637788	ACAATGAACGAAGGA[G/T]AGAGTGCAACGTTAG	9972
rs747301705	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631106	AAACTGCTAGTTGTA[C/T]ACCATTAATCATCAA	9972
rs747319749	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627282	GCTTTCCAAATAATA[C/T]GTAATTTTAGTTTTG	9972
rs747327173	snp	G/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707267	TAAAATCAAAGACAA[G/T]AGCTAATGATTTAAG	9972
rs747329695	snp	C/T	0.000271776	0.0116539	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706475	AGCCTCCCCCGCCGC[C/T]CGGCCCCGGCCCAAA	9972
rs747348682	snp	C/G	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17637594	CTATGCATTTGTTGT[C/G]TGTAACTTTGTTCTG	9972
rs747357496	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17640549	TATGGTAAAATATTA[A/C]ATAAGGGTATATGGT	9972
rs747363662	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666888	GGCAAAGCCTCTGTA[C/T]GGTTACTAACTCTTC	9972
rs747384800	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695054	AGACCCAAATACAGG[C/T]GTGTCCTTGGATCAT	9972
rs747401978	snp	A/C	3.29946e-05	0.00406155	missense	NUP153	GRCh38.p7	6:17629407	ACACCTATTTTGAAT[A/C]CTCCCTGATCTCCAA	9972
rs747419051	snp	A/C	1.64846e-05	0.0028709	missense	NUP153	GRCh38.p7	6:17616661	GTTTGTGAAGTTGAA[A/C]TTTGTAGTGCTGCTG	9972
rs747422708	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17637991	AAGATGTTTTGTTTA[C/T]AGGATATCACCTTCT	9972
rs747438162	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17685065	AAAAATGGCACTGAT[-/C]AACTTTCTTGACATG	9972
rs747457711	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17649532	CCTAATTGGTAAAAC[-/T]TGAGGGAAAAAAGAT	9972
rs747461102	snp	A/G	3.29554e-05	0.00405914	missense	NUP153	GRCh38.p7	6:17628952	CCACGTTGCCAAAAG[A/G]GAATCCTCCTTTGGT	9972
rs747512411	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17626302	ATATAGATTACTTCA[C/T]CAAATGGACATCTGT	9972
rs747513998	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673273	ACTCAGGAGGCTGAC[A/G]CAGAGAATTGCTTGA	9972
rs747549583	snp	C/T	1.64999e-05	0.00287222	missense	NUP153	GRCh38.p7	6:17661763	CAGGCAAACTGAAAT[C/T]TGGATATGAAAAGCC	9972
rs747558212	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705771	GAGACTAAGTTATTC[C/T]ACTTTCCATGTAACA	9972
rs747586849	snp	C/G	1.66854e-05	0.00288833	intron-variant	NUP153	GRCh38.p7	6:17649312	TTTCCTAAAACATAA[C/G]ATGTTGCATGATATA	9972
rs747621240	snp	C/T	3.48365e-05	0.00417337	intron-variant	NUP153	GRCh38.p7	6:17637781	GAAACCTACAATGAA[C/T]GAAGGAGAGAGTGCA	9972
rs747631427	snp	A/C	1.69178e-05	0.00290837	missense	NUP153	GRCh38.p7	6:17624787	AGCACCAAATGCTGG[A/C]CTGGCAGATGGTGCT	9972
rs747632195	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17616454	GAATCTTGATGACTT[C/T]TAAAAACAAAACATA	9972
rs747661201	snp	C/T	4.94205e-05	0.0049707	synonymous-codon	NUP153	GRCh38.p7	6:17624688	ACCAGTGGGAAATAA[C/T]GCTGTGGAAGATGAT	9972
rs747671847	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671739	TGGCTGGGCATGCTG[A/G]CTCATACCTATAATA	9972
rs747700749	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643662	GGAAAACTTAGCTCC[C/T]GTCACAAAGTAATCA	9972
rs747737862	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17654110	GCTGCACAGTTCTTT[C/G]AACATTTCATGTTTG	9972
rs747775314	snp	C/T	3.55158e-05	0.00421386	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706240	TCCAGCCGAGTTTCC[C/T]CACCCGCCAGGCCAC	9972
rs747798651	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628002	AGGAACTTGTGGATC[C/T]AACTTGGATCACTCT	9972
rs747804405	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694077	TATTGATAGCACTGA[A/G]TCACCATATTATATG	9972
rs747807343	in-del	-/AG			intron-variant	NUP153	GRCh38.p7	6:17638424	ACCCGCCAAAGAAAA[-/AG]AAATTAAAAGGAGAG	9972
rs747834772	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17652955	AATCACTTGAACCCA[C/T]GAGGCGGAGGTTGCA	9972
rs747838919	snp	C/G/T			intron-variant	NUP153	GRCh38.p7	6:17626237	CTTTTTCCTACCCTA[C/G/T]AATTGCTAGAATTTT	9972
rs747859218	snp	A/G	5.0968e-05	0.00504791	intron-variant	NUP153	GRCh38.p7	6:17674861	CAGTTAAAGTGTAAA[A/G]AAAAAGAAAAAAAAA	9972
rs747901394	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17700650	AGGACATACTTATTT[C/G]GGACAGAGTATCACA	9972
rs747927054	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17650263	CTGTTCTCTTCATGA[A/G]TTGCTGCCACTGAAT	9972
rs747957132	snp	A/G	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17637236	CACTCCCAAGATCCA[A/G]TGGGCCTTTTGAATT	9972
rs747959017	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17690833	CAGGCACTTGAATAG[A/T]AATTTCCTTACTATG	9972
rs748018299	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17684432	CTCCCTCAGACTTCA[C/G]AGAACTGAAGGGAGT	9972
rs748019112	snp	A/G	3.30006e-05	0.00406192	synonymous-codon	NUP153	GRCh38.p7	6:17626064	ATTGGAGGAAGAGGT[A/G]GAACTACCAAATATG	9972
rs748032185	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634193	CTGTTCCTTTGAAAT[C/T]CATCTTCCTCTGAAG	9972
rs748049019	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644396	TCAACATCTCCCTAA[C/T]GCAGTCAGAATAAAA	9972
rs748074459	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17621089	TCTTAAAACACAACA[C/T]ACAAATGGCCAATAG	9972
rs748099017	snp	A/G	3.29728e-05	0.00406021	missense	NUP153	GRCh38.p7	6:17665289	TGAATTCACCAGAAG[A/G]AGTCAGAGATGGTTT	9972
rs748132189	in-del	-/CA			intron-variant	NUP153	GRCh38.p7	6:17684150	TGCTGGTGCCATGCC[-/CA]CACAGTTTGCAGAAC	9972
rs748132748	snp	A/C	3.52696e-05	0.00419923	synonymous-codon	NUP153	GRCh38.p7	6:17646128	TTCTGCTGTTTTTGC[A/C]ACAGGCACACTAAAT	9972
rs748134668	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17699648	TTGAGACCACCACAC[A/C]AACATGGTGAAACCC	9972
rs748134830	in-del	-/AA	1.65682e-05	0.00287817	intron-variant	NUP153	GRCh38.p7	6:17675773	TTGTTGAAGGTTCTT[-/AA]AAAAGAAAAGCATTA	9972
rs748153910	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17672709	AACAAAAAACCTTGG[A/C]CAGGCACACCTGTAA	9972
rs748165980	snp	A/C			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632414	TGAGGCTCAATGACA[A/C]AAGAAATTTTTTTTC	9972
rs748172716	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697216	CACTGGGTATTCTCT[C/T]TCCAAGAAAGAAGGG	9972
rs748197352	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622068	TTTTCTGTGGGAATG[A/G]CCTTCACTAGACTTT	9972
rs748222897	snp	C/T	1.65833e-05	0.00287948	intron-variant	NUP153	GRCh38.p7	6:17675510	TTATGTACTACCACA[C/T]GTCAAGAATACCTTT	9972
rs748227622	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698056	GATTATAAAATCTCC[C/T]TTCTCAAATAGTTTC	9972
rs748239446	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17657612	GGCTTCTGTGCTCAT[C/T]AGGCAGTAAGGGAAA	9972
rs748254522	snp	A/C	1.64808e-05	0.00287057	missense	NUP153	GRCh38.p7	6:17625940	TTGCTAGTTTGCTAT[A/C]TTGAGAAAATAGCAA	9972
rs748256543	snp	A/G	1.66438e-05	0.00288472	synonymous-codon	NUP153	GRCh38.p7	6:17629493	GACACCAAATTTGAA[A/G]GATGAGGAGGCTGCT	9972
rs748285594	snp	A/G	1.98061e-05	0.00314685	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706400	CATGGCGGAGCCTCC[A/G]CCGCTTCCCGCTCCG	9972
rs748318662	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17616745	CAAAATGATAGGTTT[G/T]TTTGTTTGTTTGTTT	9972
rs748350011	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641116	AATGGTTTTATCGTT[A/G]TATTTTTAAGGGGCG	9972
rs748358047	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657344	GGCCAGGAGTTCGAG[A/G]CCAGCCTGGACAACA	9972
rs748373449	snp	G/T	1.64906e-05	0.00287142	missense	NUP153	GRCh38.p7	6:17675336	CTGGGGACCACAGAG[G/T]TGGCAATGAAGTGTT	9972
rs748383680	in-del	-/A	1.65726e-05	0.00287855	intron-variant	NUP153	GRCh38.p7	6:17616700	GAAAGCCGAACCTGC[-/A]ATAGTTAAAGCAGAA	9972
rs748384875	snp	C/G	3.54667e-05	0.00421095	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706444	GGCGGGAGAGGCAGA[C/G]GCGGAGGCCTTAGAG	9972
rs748385375	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	NUP153	GRCh38.p7	6:17637586	TTGACAGGCTATGCA[C/T]TTGTTGTCTGTAACT	9972
rs748400939	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17629617	AAACACTGTGAAAGC[C/T]AAAGAAACATAGGAG	9972
rs748428746	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17692295	AGCTTAATAGAGGAA[A/C]AGTGAGACAGAGACA	9972
rs748459896	snp	A/G	0.000131946	0.0081213	missense	NUP153	GRCh38.p7	6:17669431	TTTTAAAAATTTACC[A/G]CTAAAGGGCTTGACA	9972
rs748473313	snp	C/T	4.96561e-05	0.00498253	missense	NUP153	GRCh38.p7	6:17649295	TAATACTGGAACTTC[C/T]ATTTCCTAAAACATA	9972
rs748477697	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658697	TGGGTGTCTCACAAG[C/T]TGAGTGAAAATTTAA	9972
rs748484661	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17703495	CTTAATCAAATAACA[G/T]TAGTATAAAACATGC	9972
rs748511259	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	NUP153	GRCh38.p7	6:17628854	CTTCCCAAAAACTAG[A/G]GAAGTAGAAGTGACA	9972
rs748541496	snp	C/T	1.64811e-05	0.00287059	missense	NUP153	GRCh38.p7	6:17616647	CCTGATGGACTGTTG[C/T]TTGTGAAGTTGAAAT	9972
rs748541791	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17648576	GAGCCAAGATCGTGC[A/C]ACTGCACTCCAGCCT	9972
rs748545121	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17647504	ATTTCTTGGGTATGA[G/T]AGCTGTATTGTGGGG	9972
rs748554487	snp	A/G	4.94189e-05	0.00497062	missense	NUP153	GRCh38.p7	6:17637492	CTGTCCCTGATGCAG[A/G]AAGAGTTGTTTTGCC	9972
rs748601662	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17669763	AGAAATTACCTTTAC[A/G]ATAACAAAAGAATGA	9972
rs748637667	snp	A/G	1.69169e-05	0.00290829	intron-variant	NUP153	GRCh38.p7	6:17688374	CCTATCATTCATGAC[A/G]AAATATTCACATTTT	9972
rs748657402	snp	A/T	1.64925e-05	0.00287158	missense	NUP153	GRCh38.p7	6:17628751	TACTAAAACTAAATG[A/T]GGACTTTGAAGAATT	9972
rs748678065	snp	C/T	1.65018e-05	0.00287239	missense	NUP153	GRCh38.p7	6:17669526	GAGTTGCTTAGCTTT[C/T]ATTTGTCTTCTAACT	9972
rs748700733	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619339	CTCAAGAATCACTGG[A/G]AGATGTGCTGTATCA	9972
rs748708095	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687702	TTTAACATAGGGCTA[C/T]AAAAAGTTTTGTAAT	9972
rs748725398	snp	A/G	1.6577e-05	0.00287893	missense	NUP153	GRCh38.p7	6:17669333	GATGGAATTCTTTTT[A/G]CATCCTGTTAAAGTT	9972
rs748746381	snp	A/G	1.82111e-05	0.00301749	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632838	CTTGAAGCAGGTACT[A/G]AACTTCCTAAAAAAA	9972
rs748758988	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693116	ACCTATACTGTTTTT[C/T]TCTGAATCCACTCAC	9972
rs748788188	in-del	-/TTAG			intron-variant	NUP153	GRCh38.p7	6:17633986	TGTCACTGTAGTCTC[-/TTAG]TTGGTGACTCCACTG	9972
rs748789530	in-del	-/ATA			intron-variant	NUP153	GRCh38.p7	6:17651335	AATAAAAACAGAATT[-/ATA]ATAATAAATATTAAA	9972
rs748810076	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17681968	TCCCAGCACTTTTAG[C/G]AGGCTGAGGCAGGAG	9972
rs748820360	snp	A/C	1.66504e-05	0.0028853	intron-variant	NUP153	GRCh38.p7	6:17624549	ATACTAACAGCATCA[A/C]AGCACACTTACTAGA	9972
rs748826392	snp	A/C	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17629047	TTGGTTTCTATGGTT[A/C]CAAGGTTGAAGCTGC	9972
rs748904489	snp	C/T	0.000148259	0.00860858	synonymous-codon	NUP153	GRCh38.p7	6:17688472	CTCATCGGCATATAC[C/T]AGATGGTCCTCTTTA	9972
rs748904787	in-del	-/AATT			intron-variant	NUP153	GRCh38.p7	6:17643954	AATTTAATCCTCTTG[-/AATT]AATAGTTAACATTAA	9972
rs748945580	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17703404	TAACTAACAGCGCCA[C/G]ACCTCTCATTGTTTC	9972
rs748994194	snp	C/T	3.29533e-05	0.00405901	synonymous-codon	NUP153	GRCh38.p7	6:17688574	TCTTTGTAGCCACCC[C/T]GGCACAATATTCTTA	9972
rs748995034	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17647753	TAGATTTGATAAAAA[C/T]ATAACATGGCTTTGA	9972
rs749002726	snp	A/C	6.97326e-05	0.00590436	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706443	GGGCGGGAGAGGCAG[A/C]GGCGGAGGCCTTAGA	9972
rs749005000	snp	A/G	1.648e-05	0.0028705	missense	NUP153	GRCh38.p7	6:17625924	CCTGTGCTGGATGTG[A/G]TTGCTAGTTTGCTAT	9972
rs749017623	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17663069	TACAGTGTTGTGCCA[A/G]TGTTAAGTTTCTGGG	9972
rs749029886	snp	A/C	3.29799e-05	0.00406065	missense	NUP153	GRCh38.p7	6:17665282	GTCTTCCTGAATTCA[A/C]CAGAAGGAGTCAGAG	9972
rs749030364	snp	C/T	5.28434e-05	0.00513993	intron-variant	NUP153	GRCh38.p7	6:17637128	AAGTAATAAGCAAAA[C/T]TACTCCATAAAGCCA	9972
rs749033111	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619772	TCAATGCAATCCCTA[C/T]CAAAAATACCAATGA	9972
rs749045641	snp	A/C	1.81552e-05	0.00301285	intron-variant	NUP153	GRCh38.p7	6:17632857	TTCCTAAAAAAAAAA[A/C]AAAAAACGGGGAGTG	9972
rs749062402	in-del	-/AA	0.0168055	0.0901129	intron-variant	NUP153	GRCh38.p7	6:17669032	CCTATCAAGAGGCTG[-/AA]AAAAAAAAAAAACAC	9972
rs749097316	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17685246	ATATATAGTCATGTG[A/C]CACATAAGAACAGTC	9972
rs749100449	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699603	GCACTTTGGGAAGCC[A/G]AGGAGGGCAGATCAC	9972
rs749117198	snp	A/T	1.76151e-05	0.0029677	missense	NUP153	GRCh38.p7	6:17646109	TACTACTAGAACCAG[A/T]AAGTTCTGCTGTTTT	9972
rs749128739	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684135	TAAAAGCCAAGCAGA[C/T]GCTGGTGCCATGCCC	9972
rs749131881	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17672440	ATTTAGCTGGGAATG[A/G]TGGCACACGCCTGTG	9972
rs749178160	snp	A/C			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704370	TCTATTCAGACCATC[A/C]AATGACCTATATTTA	9972
rs749192517	snp	A/G	1.65067e-05	0.00287282	synonymous-codon	NUP153	GRCh38.p7	6:17625824	TGCAGAGCTAGATGT[A/G]GTTGTGGCTCCAAAG	9972
rs749194463	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642406	ATGGGTAAAGGACGT[A/G]AAAGGCATTCCTCCC	9972
rs749240113	snp	A/C	1.6498e-05	0.00287206	missense	NUP153	GRCh38.p7	6:17629390	ACCCAGAATCGGATG[A/C]CACACCTATTTTGAA	9972
rs749251260	in-del	-/AAT			intron-variant	NUP153	GRCh38.p7	6:17683352	GAAAGGTATTTCTTA[-/AAT]AATGAGACTGGAAAG	9972
rs749281292	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682666	GCTCACACCTGTAAG[C/T]CCAGCACTTCGGGAG	9972
rs749290555	in-del	-/A	1.65332e-05	0.00287512	intron-variant	NUP153	GRCh38.p7	6:17647916	TGTACCTGGTTTTCC[-/A]AATTATTAAGAAATG	9972
rs749299302	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17680238	AAGAGCCTGTGGTCT[C/G]TAATACTGTAATAAA	9972
rs749302420	snp	C/T	1.64852e-05	0.00287094	intron-variant	NUP153	GRCh38.p7	6:17662112	CGTTTGCTTATTTGT[C/T]GTAATTTTCTTAGTA	9972
rs749330998	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17628299	CCTTCCCATAGATTA[C/T]GGTAGAAAATACTTC	9972
rs749334066	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17696171	AGTTAAGGGACCCTG[A/C]CTACCAAACAGATCT	9972
rs749340558	snp	A/G	0.000317548	0.0125966	intron-variant	NUP153	GRCh38.p7	6:17675079	CCATATGAACCCAGG[A/G]GGTGGAGGTTGCAGT	9972
rs749352840	in-del	-/CATTGCA			intron-variant	NUP153	GRCh38.p7	6:17699442	GAGCCGAAATCGCAC[-/CATTGCA]CTTCAGCCTGGGTGA	9972
rs749357002	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667060	TTTATGGATACGATA[C/T]TCAACCATTAGTAAA	9972
rs749372288	snp	A/C	1.64795e-05	0.00287045	missense	NUP153	GRCh38.p7	6:17616617	GTGCTAGAATTTGCA[A/C]CAAATGTGAACACTC	9972
rs749372607	snp	C/G	3.29462e-05	0.00405857	missense	NUP153	GRCh38.p7	6:17637578	TTTGCTGCTTGACAG[C/G]CTATGCATTTGTTGT	9972
rs749382275	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697145	CATAATCATAAATAA[C/T]AAATTTAAGTTCAAG	9972
rs749418526	snp	C/T	3.32143e-05	0.00407505	synonymous-codon	NUP153	GRCh38.p7	6:17629301	TTCTTCGGGCTTAGA[C/T]TCAGATGAAACTCCA	9972
rs749464472	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639128	TGTCGCCCAGGCTGG[A/G]GTGCAGTGGTTCGAT	9972
rs749472399	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676636	CTACTGTAAACAATT[A/G]TAAGACTGGAGAAAA	9972
rs749482201	snp	A/T	1.67514e-05	0.00289403	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706323	TTAATTGGCCCCTGG[A/T]GGCAACGCCGCGTCC	9972
rs749545677	snp	A/T	1.73576e-05	0.00294593	intron-variant	NUP153	GRCh38.p7	6:17688363	GGGCATGAAAACCTA[A/T]CATTCATGACAAAAT	9972
rs749583928	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679580	TTTAAAAACAACAAA[A/G]AAGTTGGAGGTCTCA	9972
rs749598102	snp	A/G	0.00164699	0.0286493	intron-variant	NUP153	GRCh38.p7	6:17669032	CCTATCAAGAGGCTG[A/G]AAAAAAAAAAAAACA	9972
rs749604767	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633116	ACTGGTGAGCTCCCC[C/T]TTAACCACATGTTTG	9972
rs749640689	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658365	CATGCTACTGCCCTC[C/T]AGCCTGGGCCACAGA	9972
rs749645067	snp	C/T	3.29478e-05	0.00405867	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632732	ATTCTGCACTAGGCA[C/T]AATTCACAGTCCCAG	9972
rs749700541	snp	A/G/T	3.30662e-05	0.00406598	missense	NUP153	GRCh38.p7	6:17628735	TCAGATGGTTTTGTC[A/G/T]TACTAAAACTAAATG	9972
rs749706271	in-del	-/GGGGGG			downstream-variant-500B	NUP153	GRCh38.p7	6:17614635	GGGGGCGGGAGAACT[-/GGGGGG]GGGGGGGGGGGGGAG	9972
rs749749031	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17689499	CACTACAGCAAATGT[C/T]GGCTGAAAATCTCAG	9972
rs749789563	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17618757	TTTCTTAGTAGAGAT[A/G]GGGTTTCACCGTGTT	9972
rs749797151	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617887	AAGATGGTAATTCTC[C/T]TCTTCCACCGCACCA	9972
rs749852957	snp	C/T	8.48054e-05	0.00651118	synonymous-codon	NUP153	GRCh38.p7	6:17629514	GGAGGCTGCTGAGTT[C/T]GAAGATGAGGAAGAT	9972
rs749860440	snp	A/G	3.31532e-05	0.0040713	intron-variant	NUP153	GRCh38.p7	6:17675777	TTGAAGGTTCTTAAA[A/G]GAAAAGCATTAATAT	9972
rs749870658	snp	A/G	1.65263e-05	0.00287452	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639955	AGGGCTTTTCAGAAT[A/G]TCTAGAACACTTCCT	9972
rs749881788	in-del	-/A	0.00118875	0.0243508	intron-variant	NUP153	GRCh38.p7	6:17674857	ATCCAGTTAAAGTGT[-/A]AAAAAAAAAGAAAAA	9972
rs749930551	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658917	CTGGTGGTCTGCCGC[C/T]GGTCTAATCCACTAC	9972
rs749931983	snp	A/C	1.64855e-05	0.00287097	synonymous-codon	NUP153	GRCh38.p7	6:17665353	TGGCTTTGGGGTCAT[A/C]AGTCTCTGAACAGGA	9972
rs749941490	snp	C/T	4.94743e-05	0.0049734	missense	NUP153	GRCh38.p7	6:17626039	CAAACACAAAGGTAG[C/T]CACAGGTGGATTGGA	9972
rs749948103	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17647038	CTGGGATTACAGGCA[C/T]GAGCCACCGTGCCCG	9972
rs749951471	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17648348	TTGGCCAGGAGTGGG[G/T]GCTCACGCTTGTAAT	9972
rs749979764	snp	A/G	1.65021e-05	0.00287241	missense	NUP153	GRCh38.p7	6:17629456	TTGTTAAAGTCTGAG[A/G]AGGCCCAGAAGAGGA	9972
rs750022549	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17670993	TTTTTGTATTTTTAG[G/T]AGAGATAGGGTTTCA	9972
rs750024245	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658286	CTGTAATCACAGTTA[C/T]TCGGGAGGCTGAGGC	9972
rs750088741	in-del	-/AGA			intron-variant	NUP153	GRCh38.p7	6:17687624	ACAAATCAGGCAGGG[-/AGA]TGTTACTAAGTACAC	9972
rs750121807	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17630160	GGGCATAAAGAAACT[G/T]TGAAAGATTTACAAG	9972
rs750135954	snp	C/G	1.64803e-05	0.00287052	missense	NUP153	GRCh38.p7	6:17675612	TAATTTCCTTTACAA[C/G]GGAAAATCCCGAACT	9972
rs750172440	snp	C/G	5.4076e-05	0.00519953	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706428	CCGGGGCGGGTAAGG[C/G]GGCGGGAGAGGCAGA	9972
rs750176498	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17626729	ATGGACTGATATTAG[G/T]AGGACAAAGCTGCCT	9972
rs750201827	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17693894	AAGTGCACCACCACC[A/G]CGCCTGGCCTAATAC	9972
rs750207815	in-del	-/AGA	3.29489e-05	0.00405874	cds-indel	NUP153	GRCh38.p7	6:17616151	AGAGAATGAAGTTCC[-/AGA]AGAAGAGAACACATT	9972
rs750209551	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17697768	CAGCTGGGGTGGGGG[-/A]AAGGCTATTCTATAA	9972
rs750217813	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695619	GACTTACACAGAATA[C/T]GTGTTTATGATGCAC	9972
rs750256636	snp	C/G	1.65548e-05	0.002877	missense	NUP153	GRCh38.p7	6:17629384	TTATAGACCCAGAAT[C/G]GGATGACACACCTAT	9972
rs750264561	snp	C/T	1.66479e-05	0.00288508	intron-variant	NUP153	GRCh38.p7	6:17675487	AAAATTTAATGTTAC[C/T]ACCCAAATTATGTAC	9972
rs750291085	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17682258	AAAAAAATTGCTAAC[-/A]AATAACAATCTGCTG	9972
rs750372737	snp	A/G			missense	NUP153	GRCh38.p7	6:17625930	CTGGATGTGGTTGCT[A/G]GTTTGCTATCTTGAG	9972
rs750408694	snp	A/T	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17688437	GGTGTGATTCTCCCA[A/T]CAGTAATATTAGAGC	9972
rs750414033	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17672375	TTGAGCCCAGGAGTA[C/G]AACACCAGCCTAGGC	9972
rs750421500	snp	C/G	1.64822e-05	0.00287068	missense	NUP153	GRCh38.p7	6:17649269	CTGGTGATCGGTAGA[C/G]AGATTTTCGGTAATA	9972
rs750421622	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704988	GTCTGGATCTCCTGA[C/T]CTCGGTGATCCACCC	9972
rs750425829	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650273	CATGAGTTGCTGCCA[C/T]TGAATACCTGAAGTT	9972
rs750441797	snp	A/G	6.72914e-05	0.0058001	intron-variant	NUP153	GRCh38.p7	6:17669260	ATTTTTGTATGAACA[A/G]TATTTTGTAAAAAGG	9972
rs750448004	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17665988	GGCAACTCACCTGGC[-/T]TTTTTTTTTTTTTTT	9972
rs750489930	snp	C/T	1.6476e-05	0.00287014	missense	NUP153	GRCh38.p7	6:17628817	ACACTGGTTGACACT[C/T]TGGCTCTTCATTGTC	9972
rs750497570	snp	C/T	3.30366e-05	0.00406413	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632815	GAGAGACAGGTACAG[C/T]GCTGCTACTTGAAGC	9972
rs750505266	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674363	ACATTTCTTGAGATA[C/T]ACGCACATATCTAAT	9972
rs750531150	snp	A/T	1.65206e-05	0.00287403	intron-variant	NUP153	GRCh38.p7	6:17669402	GTTTTGTTACACTCC[A/T]GTATTAATCGTGATT	9972
rs750545324	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17673449	ATATAACAAAGTATT[G/T]GTACCCTGAAAAATG	9972
rs750560280	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17662406	CAAAGCTATTCCTTT[C/T]GAAATAGCTCCCTAC	9972
rs750569844	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17644979	TGGTGCCAGCTACTC[A/G]GGAGGTTGAGGAGGA	9972
rs750572965	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17651191	TGCCTGTAGTCCCAG[C/T]ACCTGGGAGGCTGAG	9972
rs750601958	in-del	-/AAGT	1.7753e-05	0.00297929	intron-variant	NUP153	GRCh38.p7	6:17637113	TAAACTGTTCAACAG[-/AAGT]AATAAGCAAAATTAC	9972
rs750618158	snp	A/G	6.59076e-05	0.00574016	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632698	TTTCACATGCCAAAC[A/G]TTTGGTAGAGTCTGC	9972
rs750629427	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17621710	GTTGGGGTGGTGGTA[C/G]GAAGGGAAGGTGGTT	9972
rs750695345	snp	A/G	1.6609e-05	0.0028817	synonymous-codon	NUP153	GRCh38.p7	6:17629292	TTTTTTAACTTCTTC[A/G]GGCTTAGATTCAGAT	9972
rs750723665	snp	G/T	1.75185e-05	0.00295955	intron-variant	NUP153	GRCh38.p7	6:17688353	TTCAAAATTAGGGCA[G/T]GAAAACCTATCATTC	9972
rs750734545	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700469	ATCCAATCCTATCAA[C/T]GTTTCCATTTCTATT	9972
rs750735736	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17621181	TAGCATTTCACCTCT[C/T]AGAATGGCTATTAGC	9972
rs750736295	snp	A/T	1.64966e-05	0.00287194	intron-variant	NUP153	GRCh38.p7	6:17661980	AGACCTTACAAGTTA[A/T]ATATAAAGAAGTATA	9972
rs750775197	in-del	-/TTTTTT			intron-variant	NUP153	GRCh38.p7	6:17618563	AAGTTAAAATCTCTC[-/TTTTTT]TTTTTTTTTTTTTTA	9972
rs750780211	snp	G/T	1.656e-05	0.00287745	missense	NUP153	GRCh38.p7	6:17624770	AATGTTGGGGTCTGG[G/T]TAGCACCAAATGCTG	9972
rs750782101	snp	C/T	6.6177e-05	0.00575188	synonymous-codon	NUP153	GRCh38.p7	6:17629202	ATTAGATACCCCAAA[C/T]TGAAATGGAGTTAAA	9972
rs750817553	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667565	TAAAAATACAAAAAA[C/T]CGGCCAGGCATGGTG	9972
rs750818803	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17669715	TTCAATTTTTTTCTT[C/T]ATGCCTTTACTGGAA	9972
rs750835158	snp	A/G	4.16155e-05	0.00456136	intron-variant	NUP153	GRCh38.p7	6:17624876	ACCATGGTGGCTAAT[A/G]TCAGATTATCCTCAA	9972
rs750870153	snp	C/T	3.29696e-05	0.00406001	missense	NUP153	GRCh38.p7	6:17629117	GGGTGGAGTTAATAA[C/T]ACCTGTACCAAAGCT	9972
rs750879389	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686604	GTTTCACCATGTTAG[C/T]CAGGATGGTCTCAAT	9972
rs750918497	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702925	AGAATTTGGGCCGGG[C/T]GCGGTGGCTCACGCC	9972
rs750932232	snp	A/G	1.64811e-05	0.00287059	synonymous-codon	NUP153	GRCh38.p7	6:17674959	AGCTGCTGCCCCACC[A/G]TATGTTGTTTTTCCA	9972
rs750932611	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619498	AGCCTGGTAGGAGGA[A/G]CAGGTTAAAAGACCC	9972
rs750971420	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17640932	CTGGCCCACAAAAAT[A/C]ATTCTTAAAAGTGTA	9972
rs751006946	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17680167	AGCCCTGAAATAAAA[C/G]TCCTGTCTGGGAAAT	9972
rs751021390	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17623129	GTGAGATTCTGTCTC[-/A]AAAAAAAAAAAAAAA	9972
rs751025482	snp	A/T	3.37427e-05	0.00410734	intron-variant	NUP153	GRCh38.p7	6:17675400	TAATCCATAGTAATA[A/T]CACCAATACAAGAGC	9972
rs751026185	snp	C/T			missense	NUP153	GRCh38.p7	6:17669473	GACTGCAATATTCGC[C/T]GAGCTGTTGAACTGG	9972
rs751055729	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685685	AGGAGTCTGCAGTCA[C/T]GCTAATGTAAATAAA	9972
rs751073367	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17657125	ATCTTCGGCTGAAGC[C/T]CAGGTTGATTATTTA	9972
rs751113540	snp	C/T	1.6569e-05	0.00287824	missense	NUP153	GRCh38.p7	6:17629372	CACTCATGGGGTTTA[C/T]AGACCCAGAATCGGA	9972
rs751137651	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697712	GATTAATGAAAGGCA[A/G]CTGGGGTGGGGGCAG	9972
rs751151863	snp	A/G	1.74458e-05	0.0029534	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706373	CCCTCCGACTCCTCC[A/G]GCTCCCGAGGCCATG	9972
rs751163571	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667896	ATTAAAAGGGCAGCA[A/G]GATATAATGATCAAC	9972
rs751187779	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17640859	AACTCCTGGCCTCAG[A/G]TGATCCTCCCACATC	9972
rs751239485	snp	C/T	1.6477e-05	0.00287024	missense	NUP153	GRCh38.p7	6:17675279	CTGGTTTTTTTGAGC[C/T]GGTGGCAGTGTGCTG	9972
rs751248804	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17627959	ATTTCCCCAAAACTT[A/C]TTATCTTCTAGGCCA	9972
rs751274010	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656314	AGGGTGGAACAGAGC[C/G]AGTGATGGGAAGGAC	9972
rs751296088	snp	A/G	0.00012095	0.00777562	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706421	TCCCGCTCCGGGGCG[A/G]GTAAGGGGGCGGGAG	9972
rs751338189	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17637121	TCAACAGAAGTAATA[A/T]GCAAAATTACTCCAT	9972
rs751343744	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17657941	GCTATTTATTTTATA[G/T]TATTTTAGACTGTGG	9972
rs751347467	snp	C/G	1.66157e-05	0.00288229	intron-variant	NUP153	GRCh38.p7	6:17649154	TGTATTTATATAATG[C/G]TTTTGTACCTTGTTT	9972
rs751353614	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676172	GTTGCTTTTATTTCA[A/G]TATGTCTAATCTTGA	9972
rs751355780	snp	C/G	1.6477e-05	0.00287024	missense	NUP153	GRCh38.p7	6:17628808	CAAAGGAAAACACTG[C/G]TTGACACTTTGGCTC	9972
rs751385817	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17634481	TCACTCTGTTGCCCA[C/G]GGTGGAGTAGAGTGG	9972
rs751386875	snp	G/T	0.00215969	0.03279	missense	NUP153	GRCh38.p7	6:17628707	GGCTTTTGCTGGCTG[G/T]TCAGATTCCTTCTCA	9972
rs751387329	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691237	CAATAGATCTACAAG[C/T]AAGCTCTCTATCAAA	9972
rs751387990	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17692809	TTTATCAAGCCCTCT[C/G]AAGTGATTCTAATAT	9972
rs751433988	snp	C/G	3.29462e-05	0.00405857	missense	NUP153	GRCh38.p7	6:17637443	GTATCACAATCCCAA[C/G]TGCCTATCACTGGTT	9972
rs751507407	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17623359	ACTGAAAAATGGCCA[-/AA]AAAAAAAAAAAAAAA	9972
rs751574128	snp	C/G	1.65263e-05	0.00287452	missense	NUP153	GRCh38.p7	6:17675755	TAATTTGAAGCAGTA[C/G]TAGTTGTTGAAGGTT	9972
rs751578322	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17633253	AAGACATAAGATGTA[A/T]ATTGTAGGCAATATC	9972
rs751592054	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17668200	CCTGCCTCAGCCTCC[A/G]GAGTAGCTGAGATTA	9972
rs751618035	snp	C/T	1.64825e-05	0.00287071	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632682	GTGCCTGGCTTTGCA[C/T]TTTCACATGCCAAAC	9972
rs751623021	snp	A/G	3.31945e-05	0.00407383	synonymous-codon	NUP153	GRCh38.p7	6:17629271	AAAATTATCATTCTT[A/G]CTATCTTTTTTAACT	9972
rs751636059	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17684430	ATCTCCCTCAGACTT[C/G]ACAGAACTGAAGGGA	9972
rs751659735	snp	A/T	7.39987e-05	0.00608226	intron-variant	NUP153	GRCh38.p7	6:17637807	GTGCAACGTTAGAGA[A/T]GCTTTATAAATCAAA	9972
rs751675873	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672324	GGTTCATGCTTGTAA[C/T]CCGAACACTTTGGGA	9972
rs751687589	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17655782	TTTTACCAAAAATTC[C/T]CACTAATTATAACTG	9972
rs751772686	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17632067	TAAGAGTTCTTTTCC[C/T]GGGACCTACTTTGGG	9972
rs751810559	snp	C/T	1.68004e-05	0.00289826	intron-variant	NUP153	GRCh38.p7	6:17669593	ACATAAAATCTAAGG[C/T]ACATATTTCATGCAG	9972
rs751868977	snp	A/G	1.7151e-05	0.00292835	synonymous-codon	NUP153	GRCh38.p7	6:17637769	CTTCGGCGATGCGAA[A/G]CCTACAATGAACGAA	9972
rs751869119	in-del	-/TTTATT	8.62984e-05	0.00656824	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632625	CGCTTTACCATCACC[-/TTTATT]TTTATTTTTTTGGCC	9972
rs751875150	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17696981	GAGGCTGAGGCAGGA[-/G]AATCACTTGAACCTG	9972
rs751877724	snp	C/T	6.7506e-05	0.00580934	intron-variant	NUP153	GRCh38.p7	6:17661829	TATTATTGTGGTCCA[C/T]AACTTGTTAACTAGA	9972
rs751885266	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643109	GGTGGCTGCACAACG[C/T]TGTCAAGGTACTAAA	9972
rs751901281	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17691254	AGCTCTCTATCAAAC[A/C]CATGAAGCCAAGTTC	9972
rs751944380	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661819	ACAACTGATATATTA[C/T]TGTGGTCCATAACTT	9972
rs751950514	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679987	AGATATGCTGCCTTG[C/T]GTACCCTACCCTGCA	9972
rs751969980	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650946	TAACATAAAGTAATC[C/T]GAAAAACATTATGGA	9972
rs751970853	snp	A/G	1.64806e-05	0.00287054	synonymous-codon	NUP153	GRCh38.p7	6:17629103	GTTAGCAGGAGCAGG[A/G]GTGGAGTTAATAACA	9972
rs751978074	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708590	CAGGTGATCTGCCCA[C/T]GGCCTCCCAAAGTGC	9972
rs751983701	snp	C/T	1.64909e-05	0.00287144	missense	NUP153	GRCh38.p7	6:17674933	TTTCGTAGTTTAGAC[C/T]GTCTTACAGCAGCTG	9972
rs751988418	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17622750	AAATTTTGTATAGGA[C/T]AGAAAGTTATAGTAT	9972
rs752002430	snp	A/C	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17661708	TCTCGTCTCATCTTG[A/C]CACCTCCACCACCTA	9972
rs752023131	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17652224	CTTCTACAGATCACT[A/G]TACCCAACAACTACA	9972
rs752057492	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17661384	TTTTACAAACAGACA[A/G]AACTATACAGTAATA	9972
rs752069052	in-del	-/AGGGGGCGGGAG	1.68729e-05	0.00290451	cds-indel, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706425	GCTCCGGGGCGGGTA[-/AGGGGGCGGGAG]AGGCAGAGGCGGAGG	9972
rs752070261	snp	A/G	5.16587e-05	0.00508199	intron-variant	NUP153	GRCh38.p7	6:17688660	CAGTTTTAGAAATTT[A/G]TCTTTTTAAAATAAG	9972
rs752076075	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17699046	GCAAACTGAAATATC[G/T]ATAGATAGAAAAGGC	9972
rs752093266	in-del	-/AAAGT			intron-variant	NUP153	GRCh38.p7	6:17699846	TCTCAAAAAAAAAGA[-/AAAGT]AAACAGTTTTAATTA	9972
rs752128665	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690497	TATTTATAGTAATTA[C/T]AATGAAAATCAAATG	9972
rs752140841	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17627843	GGGGTTTTAGCTTTG[C/G]TGTCCTAAATTTCAG	9972
rs752185003	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667627	GCTGAGGCAGGAGAA[C/T]TGCTTGAGCCCTGGA	9972
rs752185308	snp	C/T	1.69732e-05	0.00291313	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706354	GGATCTTGCCGCCAC[C/T]GCCCCCTCCGACTCC	9972
rs752196409	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618776	TTTCACCGTGTTAGC[C/T]AGGATGGTCTCGATA	9972
rs752229088	snp	A/G	1.64827e-05	0.00287073	missense	NUP153	GRCh38.p7	6:17675254	GTTCCAAAGGCAGAC[A/G]AGTTGAATGCTGGTT	9972
rs752234700	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17666710	ATTATGTAAGTACAC[A/C]AACTGTTTTGTTAAC	9972
rs752271117	snp	C/T	1.6566e-05	0.00287797	synonymous-codon	NUP153	GRCh38.p7	6:17629223	TGGAGTTAAAGAAAC[C/T]GGGTTGCTTAAACCA	9972
rs752294549	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17656275	TAGTACCTCTTTCCT[A/C]AGAAATGTGGACATT	9972
rs752350831	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17650793	ATATTTAACTATATA[A/G]AGCAAAAAGTACACA	9972
rs752352280	snp	G/T	1.67421e-05	0.00289323	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706288	ATACCTGATGCTGTT[G/T]TCGCCCCTGCTGGTA	9972
rs752366709	in-del	-/TG			intron-variant	NUP153	GRCh38.p7	6:17625187	TTGCATAATAAAGAC[-/TG]ATGTTTAATAAAACA	9972
rs752442983	snp	C/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707065	AACGGAACGCGGCTT[C/G]TCGGAAAGGAAGAGG	9972
rs752454306	snp	C/T	6.68729e-05	0.00578204	intron-variant	NUP153	GRCh38.p7	6:17649147	TGTCACCTGTATTTA[C/T]ATAATGGTTTTGTAC	9972
rs752462460	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619877	CCGAGGCGGGCAGAT[C/T]ACCTGAGGTCAGGAG	9972
rs752467206	snp	A/G/T	3.78496e-05	0.00435013	intron-variant	NUP153	GRCh38.p7	6:17669070	AATAGATGGGGAGTT[A/G/T]TGAAAAATACCTTTT	9972
rs752471902	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673501	TAAGAAAATAACCCA[A/G]TTTTTAAATGGGTGG	9972
rs752481624	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635008	AAATCGCAAAAGAAT[C/T]TCATAATGTTTTAGA	9972
rs752482128	snp	A/G	1.68641e-05	0.00290375	missense	NUP153	GRCh38.p7	6:17626152	CTAAAAACTGGCTTT[A/G]CTGCACCTTGATCTG	9972
rs752518668	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685374	AACACGGAGAAACCC[C/T]GTCTTTACTAAAAAT	9972
rs752536662	in-del	-/AA	1.80955e-05	0.00300789	intron-variant	NUP153	GRCh38.p7	6:17629552	AGCCTACAAAAATAT[-/AA]AAGACACCACATAGA	9972
rs752539688	snp	C/T	2.48352e-05	0.00352377	missense	NUP153	GRCh38.p7	6:17628676	TAGTACTAGTTTGAG[C/T]TCCAAAGGCAAAAGT	9972
rs752542293	snp	A/G	3.2956e-05	0.00405918	missense	NUP153	GRCh38.p7	6:17647889	CTGCCAGTGCTGCTC[A/G]GAGAGGTCATTTGTA	9972
rs752558794	snp	A/G	3.29571e-05	0.00405924	missense	NUP153	GRCh38.p7	6:17675641	CTGCCAATTGGGAAT[A/G]CCGAGGATGTAGATG	9972
rs752572004	snp	A/G	1.86806e-05	0.00305613	intron-variant	NUP153	GRCh38.p7	6:17629564	TATAAAAGACACCAC[A/G]TAGACACTCAATGTA	9972
rs752595098	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17646357	GGACTACAGGAACTC[A/G]CCACCACACCCGGCT	9972
rs752655039	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650009	CACTTTGATTTTTAA[C/T]CCAACTGAACAAAGA	9972
rs752685015	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645652	TGTATCACAATCTAC[A/G]TGGGCCTGCATAACC	9972
rs752706254	snp	C/T	1.6476e-05	0.00287014	missense	NUP153	GRCh38.p7	6:17661684	TTAGAAGCAACAAAG[C/T]GTGTTCTTTCTCGTC	9972
rs752750932	snp	C/T	1.70235e-05	0.00291744	synonymous-codon	NUP153	GRCh38.p7	6:17637763	ATCTATCTTCGGCGA[C/T]GCGAAACCTACAATG	9972
rs752752183	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17703645	TAAAGAAAGTCCTTA[A/T]TTTTAAGATTAAAAA	9972
rs752798412	snp	C/T	4.94898e-05	0.00497418	missense	NUP153	GRCh38.p7	6:17637691	AGAAGAAAAGCTACT[C/T]ATTGCTGGTCTTGTA	9972
rs752805738	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682423	TGAAGTTTGCCTCAT[C/T]GACTGACTATTCCTT	9972
rs752852886	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17671278	TGTCTTCTAATGTCT[G/T]TGTCTGATTTTGGTC	9972
rs752858704	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17683186	CCTCCTCCTGTAAAT[C/T]ACAAATGGTTTTTCT	9972
rs752863662	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642021	GTTTGCCAATTTAAA[A/G]AGTAGTAGGTAAAGT	9972
rs752867169	snp	C/G	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17624720	TAGATCCAAAGCCTG[C/G]GGGATTGGGCTGGCT	9972
rs752891945	snp	C/T			missense	NUP153	GRCh38.p7	6:17625853	AGCCGAAACCAGAGG[C/T]GGTAGTATTATTACT	9972
rs752900997	snp	A/T	1.64757e-05	0.00287012	synonymous-codon	NUP153	GRCh38.p7	6:17629022	TGTGAAAGGAGCCAC[A/T]GAAGCACTCTTGGTT	9972
rs752931628	snp	A/T	1.64773e-05	0.00287026	missense	NUP153	GRCh38.p7	6:17628801	GAATTCCCAAAGGAA[A/T]ACACTGGTTGACACT	9972
rs752975703	snp	A/G	0.000159245	0.00892172	intron-variant	NUP153	GRCh38.p7	6:17632891	GGAGATTTCATGAAA[A/G]TTTTAATTTACAGTA	9972
rs753000361	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17685236	TCAACAGCAGATATA[C/T]AGTCATGTGCCACAT	9972
rs753005073	snp	A/C	3.31857e-05	0.00407329	intron-variant	NUP153	GRCh38.p7	6:17661623	TGCTTTTTAAATAAA[A/C]CTCAAGAGTATATGA	9972
rs753010103	snp	A/G	1.67036e-05	0.0028899	intron-variant	NUP153	GRCh38.p7	6:17669585	TTGTTGCAACATAAA[A/G]TCTAAGGCACATATT	9972
rs753025828	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17688706	AGCCAGGCCAAGCAA[A/G]ACACAATGGTGTCCA	9972
rs753029023	snp	C/T	3.29565e-05	0.00405921	missense	NUP153	GRCh38.p7	6:17628942	GAGGCAGGCTCCACG[C/T]TGCCAAAAGAGAATC	9972
rs753030049	snp	G/T	2.02936e-05	0.00318534	intron-variant	NUP153	GRCh38.p7	6:17646176	AGAGAAAGAATATCC[G/T]TATACTTCGTTTTCA	9972
rs753042617	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17621472	TGTCCATCAACAGAT[A/G]GATACAGAAAATGTG	9972
rs753048796	snp	A/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17688545	CTGCATACATCTTCA[A/T]TCTTGTTGAAGTATC	9972
rs753087280	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690392	CTCAAAAAAAAAAGT[A/G]TGGGCTTTGGGATTG	9972
rs753105354	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659597	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	9972
rs753134891	snp	C/G	1.64895e-05	0.00287132	missense	NUP153	GRCh38.p7	6:17669507	CACCGTAAGATTGTG[C/G]ACTGAGTTGCTTAGC	9972
rs753136360	in-del	-/AGA	3.29799e-05	0.00406065	cds-indel	NUP153	GRCh38.p7	6:17665284	CTTCCTGAATTCACC[-/AGA]AGGAGTCAGAGATGG	9972
rs753236826	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620363	CAGCCAACTGATTTT[C/T]GACAATGATGACAAG	9972
rs753262201	snp	C/G	1.64798e-05	0.00287047	missense	NUP153	GRCh38.p7	6:17637211	ATTATTAGAAACACA[C/G]CATACTGAACACTCC	9972
rs753263159	in-del	-/TAT	1.66277e-05	0.00288333	intron-variant	NUP153	GRCh38.p7	6:17669564	GTAAAGTAAACCCTA[-/TAT]TATTTGTTGCAACAT	9972
rs753277606	snp	A/T	1.76362e-05	0.00296948	intron-variant	NUP153	GRCh38.p7	6:17688667	AGAAATTTATCTTTT[A/T]AAAATAAGTACCTAC	9972
rs753314232	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17688459	TATTAGAGCTCTCCT[C/T]ATCGGCATATACCAG	9972
rs753345909	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17638771	ACCCCAGATACACAA[A/G]ACAGACTATACACAT	9972
rs753362089	snp	G/T	1.66117e-05	0.00288194	missense	NUP153	GRCh38.p7	6:17626127	ACTAGAGGAACTGTT[G/T]TTCAAGAAACTAAAA	9972
rs753379420	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677255	CTACATCTACAGAAG[C/T]TCAAAATTATCATTA	9972
rs753407469	snp	A/G	0.000102485	0.00715766	intron-variant	NUP153	GRCh38.p7	6:17674854	TATTATCCAGTTAAA[A/G]TGTAAAAAAAAAGAA	9972
rs753417739	snp	A/G	3.29462e-05	0.00405857	synonymous-codon	NUP153	GRCh38.p7	6:17637319	AGTCATAGTCTCAGC[A/G]CTTTCCGAAACCACT	9972
rs753425859	snp	A/G	3.29576e-05	0.00405928	synonymous-codon	NUP153	GRCh38.p7	6:17616166	AGAAGAAGAGAACAC[A/G]TTTTTCCCATTTGAC	9972
rs753433000	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17665564	TAAGGTATGTATTCA[C/T]ATACCTATGCACATA	9972
rs753434627	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17678681	GGACACAGTGGCTCA[A/C]GCCTGTAGTCCCAAC	9972
rs753441276	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17648511	AATCCCAGCTACTCA[C/G]GAGGCTGAGGCAGGA	9972
rs753447772	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695784	GGAGGCCAAGGTGGG[C/T]GGATCATGAGGTCAG	9972
rs753469121	in-del	-/ATC	1.68476e-05	0.00290233	intron-variant	NUP153	GRCh38.p7	6:17674878	AAAAGAAAAAAAAAG[-/ATC]ATCAACCCTTCTATT	9972
rs753479082	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17659898	GGTATTTCCTTTTCA[C/G]ATAATGATATACAGT	9972
rs753537145	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17623912	ATCATTAGAGTGGAG[-/A]AAAGAGAGGAGTGTT	9972
rs753571700	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620162	AAATTCATATGGAAC[C/T]ACAGGAGTCCAAATA	9972
rs753589978	snp	G/T	1.73531e-05	0.00294555	intron-variant	NUP153	GRCh38.p7	6:17668936	AAACACAACAAAATT[G/T]TAGACAGTTTAAATA	9972
rs753606566	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641553	ACAAAACAAAACAAA[C/T]AAACAAACAAACAAA	9972
rs753633591	snp	A/G	1.65225e-05	0.00287419	synonymous-codon	NUP153	GRCh38.p7	6:17629469	AGAAGGCCCAGAAGA[A/G]GATGATGAGACACCA	9972
rs753655585	snp	A/T	1.79641e-05	0.00299696	intron-variant	NUP153	GRCh38.p7	6:17629548	TCAAAGCCTACAAAA[A/T]TATAAAAGACACCAC	9972
rs753696795	snp	C/G	0.000246526	0.0110996	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706436	GGTAAGGGGGCGGGA[C/G]AGGCAGAGGCGGAGG	9972
rs753704784	in-del	-/A	1.77093e-05	0.00297562	intron-variant	NUP153	GRCh38.p7	6:17616511	CTTCTCCATTTCAAT[-/A]AAAAAATTCTCTTAC	9972
rs753711674	snp	G/T	1.64882e-05	0.00287121	missense	NUP153	GRCh38.p7	6:17675714	GATGGCTCCGATGAA[G/T]AGAAGGCCTTGTTAA	9972
rs753713746	snp	A/G	3.3e-05	0.00406189	synonymous-codon	NUP153	GRCh38.p7	6:17665371	TCTCTGAACAGGAGG[A/G]TATTGAGAATCCACC	9972
rs753716307	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644281	GGTAATATCTCCCAA[C/T]TCATGTTTCTGCCTC	9972
rs753734566	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617118	CAAAGAATTAAAATA[C/T]TCTGGTCTTTTAATC	9972
rs753767030	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17698757	AAAAAAAAAAAAAAA[-/G]AGCTGGGAGCCTGAA	9972
rs753773165	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17666643	TCTTACAATGTAAGT[A/C]TAAATGGTAAATCAC	9972
rs753793116	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627713	TTCTAGGTTCAAGAA[C/T]ATTTTCACTTTAAGG	9972
rs753806189	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17616388	TCCTCCAGAATTATA[C/G]TATGGTAAATTTATG	9972
rs753829083	snp	A/T	1.6483e-05	0.00287076	synonymous-codon	NUP153	GRCh38.p7	6:17637676	AAACCCAATTCCACT[A/T]GAAGAAAAGCTACTT	9972
rs753829200	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17694901	GGAGAATCGCTTGAA[C/T]CCAGGACGCAGAGGT	9972
rs753831105	in-del	-/A	3.51914e-05	0.00419458	intron-variant	NUP153	GRCh38.p7	6:17626188	CAGAAATTAAGAAAC[-/A]AACATAAATCCTTAA	9972
rs753862000	snp	C/T	1.64882e-05	0.00287121	missense	NUP153	GRCh38.p7	6:17649276	TCGGTAGAGAGATTT[C/T]CGGTAATACTGGAAC	9972
rs753866793	snp	C/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708078	TTTGCCTCCCAGGTT[C/G]AAGCTATTCTCCTGC	9972
rs753879633	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17629708	GACCTATATTTAGTC[A/G]GTATGAGAATGATAT	9972
rs753890229	snp	A/G	1.66117e-05	0.00288194	intron-variant	NUP153	GRCh38.p7	6:17675499	TACTACCCAAATTAT[A/G]TACTACCACATGTCA	9972
rs753892911	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17645626	TGCTGATTTCTTCGG[-/T]TCAGAAATTATGTAT	9972
rs753899571	snp	C/T	0.000198511	0.00996073	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17651921	CAATACGGTGAGACC[C/T]TGTCTCTACAAATAA	9972
rs753906873	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17663471	GTCTTGCTATGGTGC[C/T]TGGGCTAGTCTTGAA	9972
rs753926057	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17617465	GATGTAGTGGGAATT[-/A]AAAAAAAAAAAAAAA	9972
rs753935244	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692542	AAAGAAAGGAGGGAG[A/G]ATGGGAAGAAGGAAG	9972
rs753958237	snp	C/G	1.64768e-05	0.00287021	missense	NUP153	GRCh38.p7	6:17628931	CAGATGGCAGAGAGG[C/G]AGGCTCCACGTTGCC	9972
rs753963188	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666265	CTCACACCTGTAATC[C/T]CAGCAATGTGGGAGG	9972
rs753982397	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17691000	AAAAAAAATTAGCCG[G/T]GTGTGGTGGTGTGCA	9972
rs753986604	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693544	TCTTGCTATCTTGTA[C/T]TTATTCCATTAACCA	9972
rs753989570	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17624197	GCCCCAGGAGAGAGC[A/G]CTGGACCTGGGGGTA	9972
rs754019949	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641047	ACTGCTTTTACTTTT[C/T]ATGCTTTCTAAACTT	9972
rs754041775	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635875	ATCCAAGTTCTTTAA[C/T]ACATATGTGAGCTTC	9972
rs754054738	snp	G/T	1.64751e-05	0.00287007	missense	NUP153	GRCh38.p7	6:17628831	TTTGGCTCTTCATTG[G/T]CAGCTTTCTTCCCAA	9972
rs754070210	snp	A/G	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17688443	ATTCTCCCATCAGTA[A/G]TATTAGAGCTCTCCT	9972
rs754129810	in-del	-/TGATA	1.67146e-05	0.00289085	intron-variant	NUP153	GRCh38.p7	6:17661809	GAAAATTAAAACAAC[-/TGATA]TATTATTGTGGTCCA	9972
rs754159889	snp	A/G	1.65089e-05	0.00287301	intron-variant	NUP153	GRCh38.p7	6:17669412	ACTCCTGTATTAATC[A/G]TGATTTTAAAAATTT	9972
rs754167173	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702619	AGGCAGAGGTTGCAC[C/T]GAGCCGAGATTGCAC	9972
rs754181067	snp	G/T	1.65669e-05	0.00287805	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632824	GTACAGTGCTGCTAC[G/T]TGAAGCAGGTACTGA	9972
rs754181279	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	NUP153	GRCh38.p7	6:17688532	GTCTGTTGAACAGCT[A/G]CATACATCTTCATTC	9972
rs754227829	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17682307	ATCTTTTAGGTGGTG[G/T]TAACAGGTCTTTGCC	9972
rs754229775	snp	A/C	3.31664e-05	0.00407211	missense	NUP153	GRCh38.p7	6:17629359	AATTTAAAGCCTTCA[A/C]TCATGGGGTTTATAG	9972
rs754258144	snp	G/T	2.3588e-05	0.00343416	intron-variant	NUP153	GRCh38.p7	6:17646058	AAAATGTAAGAAATT[G/T]TTACTTACCTGAACT	9972
rs754263932	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17649812	TTAAATTTCATCATA[G/T]ATATGTATGTATAAG	9972
rs754300916	snp	A/C	1.72728e-05	0.00293872	intron-variant	NUP153	GRCh38.p7	6:17625764	GACACACTAATAAGT[A/C]AAGTCCATCCAATTA	9972
rs754341130	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17619772	TCAATGCAATCCCTA[-/C]CAAAAATACCAATGA	9972
rs754375034	snp	C/T	4.94181e-05	0.00497057	synonymous-codon	NUP153	GRCh38.p7	6:17637325	AGTCTCAGCACTTTC[C/T]GAAACCACTGTCAAT	9972
rs754385761	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17630480	GCCTGGCCAACATGG[C/T]GAAACCCCATCTCTA	9972
rs754386049	snp	A/C	6.59196e-05	0.00574068	intron-variant	NUP153	GRCh38.p7	6:17662089	CAGGGGAAATACACA[A/C]ATATTTACGTTTGCT	9972
rs754433806	in-del	-/GTTGT	3.29468e-05	0.00405861	frameshift-variant	NUP153	GRCh38.p7	6:17637497	CCTGATGCAGAAAGA[-/GTTGT]TTTGCCACTTTTATT	9972
rs754442215	snp	A/G	1.6476e-05	0.00287014	missense	NUP153	GRCh38.p7	6:17629051	TTTCTATGGTTCCAA[A/G]GTTGAAGCTGCTCTT	9972
rs754493482	snp	A/G	1.65416e-05	0.00287586	intron-variant	NUP153	GRCh38.p7	6:17674858	ATCCAGTTAAAGTGT[A/G]AAAAAAAAGAAAAAA	9972
rs754543239	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17666661	AATGGTAAATCACTG[G/T]TAAGACTTCCAAACT	9972
rs754630293	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677267	AAGTTCAAAATTATC[A/G]TTAACTGAACTGCCT	9972
rs754641449	snp	A/G	4.75421e-05	0.00487532	intron-variant	NUP153	GRCh38.p7	6:17646202	TTTCAATAAGTATCA[A/G]ATATAGAGCTTTTTT	9972
rs754648035	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676570	TGTTTCTAAAGTTCC[C/T]AAAAAGAGGCTTCCA	9972
rs754707742	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684578	TTATCCTTTGTGTGT[C/T]TACTAGAGCAGCACT	9972
rs754708045	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17633731	TAGTGCTGACAGTGA[A/T]GCCATTCATTCTGGT	9972
rs754723586	snp	A/G	1.64993e-05	0.00287218	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616053	AGTATCTGAAAGCAG[A/G]GCACCAGCTGTTGTT	9972
rs754727992	snp	A/G	1.81876e-05	0.00301554	intron-variant	NUP153	GRCh38.p7	6:17629553	GCCTACAAAAATATA[A/G]AAGACACCACATAGA	9972
rs754738752	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17617188	TTGACACCTCCAACA[A/C]ATCACACAACTTACC	9972
rs754774754	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17629790	GCGATAAAGTTTGAT[-/A]AAAGTTTGTACTAGT	9972
rs754776163	snp	C/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706512	CCCGCGCTGTCCACA[C/G]AGTGGGCACAAGCAC	9972
rs754783799	in-del	-/AA	1.65946e-05	0.00288046	intron-variant	NUP153	GRCh38.p7	6:17675190	AAGCAATAAACACTC[-/AA]AACTAATGTGATTAA	9972
rs754811423	snp	G/T	1.66358e-05	0.00288402	missense	NUP153	GRCh38.p7	6:17626133	GGAACTGTTGTTCAA[G/T]AAACTAAAAACTGGC	9972
rs754863381	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685787	TGATAATAAATGACT[A/G]TGTAACTGTTTTATG	9972
rs754880243	in-del	-/ATATT			intron-variant	NUP153	GRCh38.p7	6:17624026	ACCCCTTTCTACATA[-/ATATT]ATATTTCACAATTAG	9972
rs754906279	snp	A/G	1.64792e-05	0.00287042	missense	NUP153	GRCh38.p7	6:17675632	AATCCCGAACTGCCA[A/G]TTGGGAATGCCGAGG	9972
rs754927081	snp	A/C	4.98045e-05	0.00498997	intron-variant	NUP153	GRCh38.p7	6:17675502	TACCCAAATTATGTA[A/C]TACCACATGTCAAGA	9972
rs754937718	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17683548	AGGTCTCAACAACTG[A/G]CTTAAAATGTTCAGT	9972
rs754953798	snp	A/G	1.65332e-05	0.00287512	missense	NUP153	GRCh38.p7	6:17629473	GGCCCAGAAGAGGAT[A/G]ATGAGACACCAAATT	9972
rs754967251	snp	A/G	1.64879e-05	0.00287118	synonymous-codon	NUP153	GRCh38.p7	6:17665284	CTTCCTGAATTCACC[A/G]GAAGGAGTCAGAGAT	9972
rs754981021	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17653576	CCAGAGAAATAAATT[G/T]ATTTACGAAAAGACC	9972
rs754988805	snp	C/G/T	3.29464e-05	0.00405861	missense	NUP153	GRCh38.p7	6:17637582	CTGCTTGACAGGCTA[C/G/T]GCATTTGTTGTCTGT	9972
rs755024736	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656135	GCTTGAACTCAGGAG[A/G]TGGAGGTTGCAGTGA	9972
rs755034019	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641915	TTGAAGCTGGCTAAA[C/T]AGTATATGGGGATTC	9972
rs755053700	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641077	TGCATCCTTGTATTT[A/G]GAGATCTACATTTTC	9972
rs755057015	snp	A/T	1.66607e-05	0.00288619	intron-variant	NUP153	GRCh38.p7	6:17616724	AGCAGAAATACTTCA[A/T]TAGGGCAAAATGATA	9972
rs755057853	snp	A/C	1.64749e-05	0.00287005	synonymous-codon	NUP153	GRCh38.p7	6:17647834	TAGTACATTTGCCTC[A/C]GTAGATTTTACGATT	9972
rs755062586	in-del	-/C	1.65356e-05	0.00287533	frameshift-variant	NUP153	GRCh38.p7	6:17616565	TGGTTAAATGGAAAG[-/C]CCCCCCGAGCCTGAA	9972
rs755123196	snp	C/G	3.48888e-05	0.0041765	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706442	GGGGCGGGAGAGGCA[C/G]AGGCGGAGGCCTTAG	9972
rs755146558	snp	A/G	1.65064e-05	0.00287279	intron-variant	NUP153	GRCh38.p7	6:17669415	CCTGTATTAATCGTG[A/G]TTTTAAAAATTTACC	9972
rs755147509	in-del	-/GA			intron-variant	NUP153	GRCh38.p7	6:17667956	TTTTGTTTGGCTGAT[-/GA]GAGATCTGCCTAATT	9972
rs755219380	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679019	CAATTCTGGATTATT[C/T]AGTTCCAAAGTACTA	9972
rs755234862	snp	A/C	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17628849	GCTTTCTTCCCAAAA[A/C]CTAGGGAAGTAGAAG	9972
rs755239745	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17701023	TTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGATC	9972
rs755278034	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17692584	AATGGACCTGGAACC[A/C]GTATGAAGGAACAAA	9972
rs755284457	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17652665	GGGAAAAAAATATTT[C/G]TTAAGAAATGTATCT	9972
rs755288601	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17624256	AGGATCAGAAAATGC[A/T]CTTCAAAGCTAGCCT	9972
rs755300908	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687335	ACAGAAAAAGAAAAG[C/T]CAGAGTCCCTTTCAC	9972
rs755327459	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659220	ACACTTCCGCAACAG[C/T]GGGATGCAGAAAATG	9972
rs755338205	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17626867	ATTATGGGAGGAGGA[A/C]GGGAATACCTTCACC	9972
rs755345167	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17681229	AAAAAAAAAACGGAC[C/T]CAAAAGAACTCATGG	9972
rs755348641	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17648529	GGCTGAGGCAGGATA[A/T]CCACTTGAACCCGGG	9972
rs755357755	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17620215	AGAAAAAAGCTGAGG[C/T]ATCATACTATCTGAC	9972
rs755368963	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17703655	CTTATTTTTAAGATT[-/A]AAAAAAAAAAAAAAG	9972
rs755406305	in-del	-/AC	3.29473e-05	0.00405864	frameshift-variant	NUP153	GRCh38.p7	6:17637501	TGCAGAAAGAGTTGT[-/AC]TTTGCCACTTTTATT	9972
rs755408565	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619263	AAATCTTACCAAACA[C/T]GGGGAGAGAATAAAG	9972
rs755473755	snp	A/G	1.64808e-05	0.00287057	intron-variant	NUP153	GRCh38.p7	6:17662090	AGGGGAAATACACAC[A/G]TATTTACGTTTGCTT	9972
rs755480500	snp	A/G/T	3.30542e-05	0.00406524	missense, synonymous-codon	NUP153	GRCh38.p7	6:17637184	ACAGGACACACACTT[A/G/T]TTGTCTTCTGCATTA	9972
rs755488421	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17659532	GGCTGGAGTACACTG[A/G]TGCAATCTTGGCTCA	9972
rs755542464	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17682374	GTAGTGAAGGCTGGG[A/T]TGGTTGTAGCAATTT	9972
rs755553642	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17671192	TTCCTTTTTAAATTT[C/G]TTGGATTCCATTTAC	9972
rs755579906	snp	A/G	0.000181298	0.00951926	missense	NUP153	GRCh38.p7	6:17625858	AAACCAGAGGTGGTA[A/G]TATTATTACTGCTGG	9972
rs755626619	snp	A/C			synonymous-codon	NUP153	GRCh38.p7	6:17637310	AGATGAAGCAGTCAT[A/C]GTCTCAGCACTTTCC	9972
rs755627596	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17676470	AGTTACTCCACCCCA[C/G]CTTCCCGTTATTAAA	9972
rs755657637	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17668592	CTCACACCTTAGTCC[A/C]GGCACTTTGGGAGGC	9972
rs755669932	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17634981	ACAAATTAAAAAATA[-/A]AAAAAAAAAATAAAT	9972
rs755698438	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697803	AACTCAGAAACAGCT[A/G]GGGTGGGGGAAGGCT	9972
rs755733087	snp	C/T	1.64885e-05	0.00287123	missense	NUP153	GRCh38.p7	6:17665360	GGGGTCATAAGTCTC[C/T]GAACAGGAGGATATT	9972
rs755742088	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658014	TCGAGTTCAAAATGG[A/G]TTGTAAAGCAGCAAA	9972
rs755772542	in-del	-/CT			intron-variant	NUP153	GRCh38.p7	6:17688238	TTAATAAATAAAACA[-/CT]GATAAATAAAAAAGA	9972
rs755775678	snp	A/C	1.65018e-05	0.00287239	synonymous-codon	NUP153	GRCh38.p7	6:17629457	TGTTAAAGTCTGAGA[A/C]GGCCCAGAAGAGGAT	9972
rs755816459	snp	A/C	1.772e-05	0.00297652	synonymous-codon	NUP153	GRCh38.p7	6:17646104	TAAAGTACTACTAGA[A/C]CCAGAAAGTTCTGCT	9972
rs755847100	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17694841	AAAAGTAGCCGGGCA[C/T]GGTGGTGGGCACCTG	9972
rs755861093	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687188	TTGAAGTTAGTTAAT[C/T]CTTTCAAATATGCTC	9972
rs755869277	snp	C/T	4.94784e-05	0.00497361	synonymous-codon	NUP153	GRCh38.p7	6:17626046	AAAGGTAGCCACAGG[C/T]GGATTGGAGGAAGAG	9972
rs756022354	snp	A/G	1.66333e-05	0.00288381	intron-variant	NUP153	GRCh38.p7	6:17675492	TTAATGTTACTACCC[A/G]AATTATGTACTACCA	9972
rs756036223	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17672415	GACCCTGTCACTACC[-/A]AAAAAAAAAATTTAG	9972
rs756053389	snp	A/G	3.54014e-05	0.00420707	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706380	ACTCCTCCGGCTCCC[A/G]AGGCCATGGCGGAGC	9972
rs756054809	snp	C/T			missense	NUP153	GRCh38.p7	6:17665331	TTCGATTTGTTGCTA[C/T]GGAAACTGGCTTTGG	9972
rs756058586	snp	A/G	1.64735e-05	0.00286993	missense	NUP153	GRCh38.p7	6:17637566	CTGGGTGACAATTTT[A/G]CTGCTTGACAGGCTA	9972
rs756071154	snp	A/C	1.66208e-05	0.00288273	intron-variant	NUP153	GRCh38.p7	6:17616711	CTGCAATAGTTAAAG[A/C]AGAAATACTTCATTA	9972
rs756080390	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691519	CCTGTAATCTCAGCA[C/T]TTTGGGAGGCCGAGT	9972
rs756116597	in-del	-/AAAC			intron-variant	NUP153	GRCh38.p7	6:17641546	CTCAAAAACAAAACA[-/AAAC]AAACAAACAAACAAA	9972
rs756128380	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17653943	ACTTCACGCTATGTA[C/T]GCTGACGTATTTGGG	9972
rs756133600	snp	C/T	6.60731e-05	0.00574736	intron-variant	NUP153	GRCh38.p7	6:17669404	TTTGTTACACTCCTG[C/T]ATTAATCGTGATTTT	9972
rs756141829	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17673441	CGCAAAACATATAAC[-/A]AAGTATTTGTACCCT	9972
rs756152096	snp	A/C	3.29549e-05	0.00405911	synonymous-codon	NUP153	GRCh38.p7	6:17675307	CTGTGAGAGTGAGTG[A/C]GAACGTTCAGCTTCT	9972
rs756196274	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17663808	CAAGTTAAATGACAC[-/A]AAAAAACCAGACAAA	9972
rs756221599	snp	C/G	1.64757e-05	0.00287012	missense	NUP153	GRCh38.p7	6:17628826	GACACTTTGGCTCTT[C/G]ATTGTCAGCTTTCTT	9972
rs756230394	snp	A/T	1.64825e-05	0.00287071	synonymous-codon	NUP153	GRCh38.p7	6:17616598	CTGGGCTGAGGCTGC[A/T]GGTGTGCTAGAATTT	9972
rs756261470	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17637149	CATAAAGCCAAAAAC[A/G]TACCTGGTTTCTCAG	9972
rs756352194	in-del	-/AAAA			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632321	AACAAACAAACAAAC[-/AAAA]AAACAAACAAACAAA	9972
rs756357398	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673472	GAAAAATGAACTCTC[C/T]CAAAATTTATTAATA	9972
rs756371158	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17700604	CCCTCCTTTTCAAAT[C/G]TGAGAACACTCCAGC	9972
rs756379870	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690707	AATGACTCAGTAGGT[A/G]CAGAAAACAATAAAA	9972
rs756386059	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17665886	TAGAGACAGGGTCTC[A/G]CCATGTTGCTCAGGC	9972
rs756419374	snp	A/G	3.4559e-05	0.00415672	intron-variant	NUP153	GRCh38.p7	6:17625758	AGAACTGACACACTA[A/G]TAAGTAAAGTCCATC	9972
rs756420482	snp	A/C			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615963	TGTAACGAAAGAGAA[A/C]GGAGGAAAATTCCAA	9972
rs756435014	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17696944	TGGCAGGTGGTGTCC[A/G]CCTGTAATCCCAGCT	9972
rs756438723	snp	A/T	1.65586e-05	0.00287733	missense, intron-variant	NUP153	GRCh38.p7	6:17639946	TATCTTACCAGGGCT[A/T]TTCAGAATATCTAGA	9972
rs756452358	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622947	CACCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	9972
rs756467723	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618745	TAATTTTTTGTATTT[C/T]TTAGTAGAGATGGGG	9972
rs756474893	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658293	CACAGTTACTCGGGA[A/G]GCTGAGGCACAAAAA	9972
rs756517954	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630219	GGAGGGAAGGTGGAA[A/G]AAGAGACAATGGAGA	9972
rs756541247	snp	C/T	1.65597e-05	0.00287743	synonymous-codon	NUP153	GRCh38.p7	6:17675769	ACTAGTTGTTGAAGG[C/T]TCTTAAAAGAAAAGC	9972
rs756558769	in-del	-/AGAT			intron-variant	NUP153	GRCh38.p7	6:17663144	AGAACACAGAGAAAA[-/AGAT]AGAGCAAATGTAGTA	9972
rs756558867	in-del	-/TTA	1.65455e-05	0.00287619	cds-indel	NUP153	GRCh38.p7	6:17637182	ATACAGGACACACAC[-/TTA]TTGTCTTCTGCATTA	9972
rs756564301	snp	C/T	4.94564e-05	0.0049725	missense	NUP153	GRCh38.p7	6:17629120	TGGAGTTAATAACAC[C/T]TGTACCAAAGCTAAA	9972
rs756566413	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17680171	CTGAAATAAAAGTCC[G/T]GTCTGGGAAATCTGC	9972
rs756570524	snp	C/T	3.29598e-05	0.00405941	missense	NUP153	GRCh38.p7	6:17661741	CCAGAAGATAAACCA[C/T]TGGCTGCAGGCAAAC	9972
rs756605719	snp	C/G	1.648e-05	0.0028705	missense	NUP153	GRCh38.p7	6:17674966	GCCCCACCGTATGTT[C/G]TTTTTCCAGGATAAA	9972
rs756654058	snp	C/T	1.6495e-05	0.0028718	intron-variant	NUP153	GRCh38.p7	6:17661982	ACCTTACAAGTTAAA[C/T]ATAAAGAAGTATAGC	9972
rs756686782	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17681164	ATTAAGTGAAATACA[A/C]CAGGCACAAAAAGAC	9972
rs756688208	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17645837	TTTGCTACCATGCCT[A/G]TCTCTCTCAAAACCA	9972
rs756692239	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656323	CAGAGCCAGTGATGG[C/G]AAGGACTGGGTGAAG	9972
rs756697659	snp	G/T	1.66164e-05	0.00288235	missense, intron-variant	NUP153	GRCh38.p7	6:17640062	CTGTAGTGACATGAT[G/T]AGCTGTAATTTTTTT	9972
rs756717719	in-del	-/ATT	8.54474e-05	0.00653578	intron-variant	NUP153	GRCh38.p7	6:17640090	TTTAAATTTAATAAC[-/ATT]ATGCCAAATAAAACA	9972
rs756774786	in-del	-/TATGGA	1.64792e-05	0.00287042	cds-indel	NUP153	GRCh38.p7	6:17665329	ACTTCGATTTGTTGC[-/TATGGA]AACTGGCTTTGGGGT	9972
rs756798667	in-del	-/AAAAAAC			intron-variant	NUP153	GRCh38.p7	6:17672676	CACACCCATATGTTA[-/AAAAAAC]AAAAAACAAAAAACA	9972
rs756810356	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17635289	TAATTTTTTGTATTG[A/T]TAGTAGAGACAGGGG	9972
rs756851087	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17655201	TATATTTAATGACTA[C/T]AATCCTTGCACATTT	9972
rs756915230	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657170	CTGTCTTGCAGATAC[A/G]TGTTTGGTGTGACTT	9972
rs756922360	snp	G/T	1.64762e-05	0.00287016	missense	NUP153	GRCh38.p7	6:17675288	TTGAGCTGGTGGCAG[G/T]GTGCTGTGAGAGTGA	9972
rs756923507	snp	A/C	9.91654e-05	0.0070408	missense	NUP153	GRCh38.p7	6:17629182	TTCTTTTCTTCCTGT[A/C]CAAGATTAGATACCC	9972
rs756935695	snp	A/T	1.6473e-05	0.00286988	missense	NUP153	GRCh38.p7	6:17637444	TATCACAATCCCAAG[A/T]GCCTATCACTGGTTT	9972
rs756939765	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692870	ATACATTTTAGAGAA[A/G]CCCCTCCAAAACAGA	9972
rs756959925	snp	C/T	1.65968e-05	0.00288065	missense	NUP153	GRCh38.p7	6:17629272	AAATTATCATTCTTA[C/T]TATCTTTTTTAACTT	9972
rs756960347	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17663949	ACACACAAACACACA[A/C]AAAAACACTTATACA	9972
rs757002414	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17696763	CCATCTCAAAAAAAT[A/G]AAACAAATAAATAAA	9972
rs757010399	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704946	TTGTATTTGTTAGTA[A/G]GGACGGGGTTTCACC	9972
rs757010696	snp	C/G	1.65611e-05	0.00287755	missense	NUP153	GRCh38.p7	6:17629380	GGGTTTATAGACCCA[C/G]AATCGGATGACACAC	9972
rs757055346	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17653717	AAATGAGAACAGTGA[C/T]TGCCTCTGGGGTAGG	9972
rs757083732	snp	C/T	3.29647e-05	0.00405971	missense	NUP153	GRCh38.p7	6:17625861	CCAGAGGTGGTAGTA[C/T]TATTACTGCTGGCTC	9972
rs757110023	in-del	-/TTACTCATA			intron-variant	NUP153	GRCh38.p7	6:17636372	GAAGATTCTAAAATC[-/TTACTCATA]GGGAAATATCCAGTA	9972
rs757127534	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691292	CTAACTACTGAACAA[C/T]ACCAATTCACTGTTC	9972
rs757137188	snp	A/G	0.000144648	0.00850312	intron-variant	NUP153	GRCh38.p7	6:17624839	AAGGAGGATCCTGGA[A/G]GCCCAAAGAAACACT	9972
rs757161340	snp	A/C	3.49485e-05	0.00418008	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706375	CTCCGACTCCTCCGG[A/C]TCCCGAGGCCATGGC	9972
rs757179636	snp	G/T	1.68491e-05	0.00290245	intron-variant	NUP153	GRCh38.p7	6:17669250	CACCCGGCTAATTTT[G/T]GTATGAACAATATTT	9972
rs757190188	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636091	GTAATCCCAGCACTT[C/T]GGAAGGCCAAGGCGG	9972
rs757211349	snp	C/G	1.64765e-05	0.00287019	missense	NUP153	GRCh38.p7	6:17628811	AGGAAAACACTGGTT[C/G]ACACTTTGGCTCTTC	9972
rs757234563	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17662942	GAACAAAAAACAAAA[A/G]GAACTGTTCTAGACT	9972
rs757248191	snp	A/T	3.58339e-05	0.00423269	intron-variant	NUP153	GRCh38.p7	6:17626197	AGAAACAAACATAAA[A/T]CCTTAAGAATAGTCT	9972
rs757252643	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17621610	AGGCACAAAGACACA[C/T]ATTCAATGTTCTCAC	9972
rs757253210	snp	A/C/G	3.33607e-05	0.00408405	intron-variant	NUP153	GRCh38.p7	6:17616204	AAATAAAAACTTCAT[A/C/G]ATGTGACATGATGCT	9972
rs757365448	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17660199	TCTAAGACATCCAAC[A/G]ACTTCAACCAAAACA	9972
rs757372493	snp	C/T	1.69075e-05	0.00290748	synonymous-codon	NUP153	GRCh38.p7	6:17628713	TGCTGGCTGTTCAGA[C/T]TCCTTCTCAGATGGT	9972
rs757375258	snp	C/T	1.7447e-05	0.0029535	missense, intron-variant	NUP153	GRCh38.p7	6:17668997	CTTTTGGCCTGAAAA[C/T]CTGTGATATCTATCC	9972
rs757415221	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17671480	ATGAACTCAATTCAC[A/T]GAAAAGATAAAAGTT	9972
rs757499762	snp	C/T	1.65381e-05	0.00287555	missense	NUP153	GRCh38.p7	6:17675759	TTGAAGCAGTACTAG[C/T]TGTTGAAGGTTCTTA	9972
rs757503830	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659916	AATGATATACAGTAA[C/T]AGATTCCCTCCCTTC	9972
rs757504081	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17685699	ATGCTAATGTAAATA[A/C]ACTCAGTGTTACCAG	9972
rs757532068	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17618813	CCTCGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA	9972
rs757540672	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17672327	TCATGCTTGTAATCC[A/G]AACACTTTGGGAAGC	9972
rs757551698	in-del	-/A/AA/AAA/T	0.000622839	0.0176387	splice-acceptor-variant, intron-variant	NUP153	GRCh38.p7	6:17632845	AGGTACTGAACTTCC[-/A/AA/AAA/T]TAAAAAAAAAAAAAA	9972
rs757568573	snp	C/T	1.64776e-05	0.00287028	missense	NUP153	GRCh38.p7	6:17624734	GGGGGATTGGGCTGG[C/T]TGGCACCTTGACTTT	9972
rs757593706	snp	C/T	1.64743e-05	0.00287	missense	NUP153	GRCh38.p7	6:17624642	GGCTACTGCTTGACA[C/T]TGTCCCAAAAGTAGG	9972
rs757605154	snp	C/T	1.68664e-05	0.00290395	intron-variant	NUP153	GRCh38.p7	6:17639890	CAAAATGACATTAAA[C/T]TGAGATCATGAGTTT	9972
rs757614155	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639753	AGAAATTTCATTTTA[A/G]TATAGAGTCCTTTGG	9972
rs757621059	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667960	GTTTGGCTGATGAGA[A/G]ATCTGCCTAATTGAA	9972
rs757666083	in-del	-/GAGAGGGGAGGGGAGACAAGAGGGGAGAGGGGAGGG			intron-variant	NUP153	GRCh38.p7	6:17630710	GAGGAGACGGGAGAC[lengthTooLong]GAGAAGGGAGGGGAG	9972
rs757751536	snp	A/T	3.29864e-05	0.00406105	missense	NUP153	GRCh38.p7	6:17637196	CTTATTGTCTTCTGC[A/T]TTATTAGAAACACAG	9972
rs757765519	snp	C/T	1.72178e-05	0.00293404	intron-variant	NUP153	GRCh38.p7	6:17688661	AGTTTTAGAAATTTA[C/T]CTTTTTAAAATAAGT	9972
rs757766943	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638943	AATCCTCCTAAATCC[C/T]GTTGTAAAAGCCAAC	9972
rs757800660	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679343	AAAGATGTGCACATG[A/G]AAACTACAAAACAGT	9972
rs757803893	snp	A/G	1.6569e-05	0.00287824	synonymous-codon	NUP153	GRCh38.p7	6:17629226	AGTTAAAGAAACTGG[A/G]TTGCTTAAACCAGAA	9972
rs757842374	snp	A/G	1.65649e-05	0.00287788	intron-variant	NUP153	GRCh38.p7	6:17661631	AAATAAACCTCAAGA[A/G]TATATGAGTATACAA	9972
rs757863134	snp	C/G			missense	NUP153	GRCh38.p7	6:17616546	CTGTAAATGCTGCTG[C/G]AGACTGGTTAAATGG	9972
rs757870148	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17671718	ACTCAAATGCAATCT[-/C]AATCATGGCTGGGCA	9972
rs757895762	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17698425	GGCGAAACCCTGTCT[A/C]TACCGAAAAAATACA	9972
rs757918169	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17639677	GTTTACTTACTCTTA[C/T]TCCTCACTGACCTAC	9972
rs757921343	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17627952	CTTTGATATTTCCCC[A/G]AAACTTCTTATCTTC	9972
rs757955887	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673096	ACTTCTGGCTGGGCG[C/T]GGTGGCTCACGCCTG	9972
rs757956039	snp	A/G	1.64885e-05	0.00287123	intron-variant	NUP153	GRCh38.p7	6:17661995	AATATAAAGAAGTAT[A/G]GCTGTATAAGAAATG	9972
rs757979701	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17679181	CCAAAAGCTGTTAGA[C/G]CAAATTTAGCCAAGT	9972
rs757991388	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17657114	AAAGTTCTGAGATCT[G/T]CGGCTGAAGCTCAGG	9972
rs757993492	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17644499	TTGCAATTCTAAAGC[A/G]TGTCATGCTTTTTCT	9972
rs758009928	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17682925	GTCTCAAAAAAGAAG[-/AA]AAAAAAAAAAAAAAA	9972
rs758012656	snp	G/T	5.01995e-05	0.00500972	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706291	CCTGATGCTGTTGTC[G/T]CCCCTGCTGGTAAGG	9972
rs758020737	snp	A/G			missense	NUP153	GRCh38.p7	6:17675317	GAGTGAGAACGTTCA[A/G]CTTCTGGGGACCACA	9972
rs758030923	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666758	AAACATAGTAAAAAT[C/T]CTGTTGGTATAAAAC	9972
rs758072604	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17663899	AGCAATTCTATTTCT[-/A]GGTATAAACCCAAGA	9972
rs758082785	snp	C/T	3.29587e-05	0.00405934	missense	NUP153	GRCh38.p7	6:17674990	GGATAAAAAGGAGAA[C/T]CTCCAAGCTGACTGG	9972
rs758091662	snp	A/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707088	GGAAGAGGGACGGGG[A/G]AGGAGATCTCCGGGG	9972
rs758118348	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	NUP153	GRCh38.p7	6:17637340	CGAAACCACTGTCAA[C/T]GTAAGGGCTCGCTTC	9972
rs758118349	snp	C/T	3.33784e-05	0.0040851	intron-variant	NUP153	GRCh38.p7	6:17649149	TCACCTGTATTTATA[C/T]AATGGTTTTGTACCT	9972
rs758144625	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708499	AGGCATGTGCCACGA[C/T]GGCCGGCTAATTTTG	9972
rs758171433	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	NUP153	GRCh38.p7	6:17637423	GTTTATTTTGCACTA[A/G]ACAGGTATCACAATC	9972
rs758184659	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635917	TGTAACAAATTACTT[C/T]CTGACTCAAAGTTTT	9972
rs758196257	snp	C/T	1.76827e-05	0.00297339	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706243	AGCCGAGTTTCCCCA[C/T]CCGCCAGGCCACCGC	9972
rs758200350	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666388	GGCGTGGTGGCATGC[A/G]CCTGTAATCCCGGCT	9972
rs758208111	snp	A/C	1.64803e-05	0.00287052	synonymous-codon	NUP153	GRCh38.p7	6:17647891	GCCAGTGCTGCTCGG[A/C]GAGGTCATTTGTACC	9972
rs758320159	snp	A/G	5.73702e-05	0.00535554	intron-variant	NUP153	GRCh38.p7	6:17629579	ATAGACACTCAATGT[A/G]CTGATCCTCTCAAAC	9972
rs758339665	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17684677	CAGGCCTGTCTCAGC[G/T]GTCCACATGCCTTCC	9972
rs758375065	snp	A/G	1.72033e-05	0.0029328	intron-variant	NUP153	GRCh38.p7	6:17626169	TGCACCTTGATCTGT[A/G]AGACAGAAATTAAGA	9972
rs758375276	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17673619	ACATGCAACATCATT[A/C]GTCATTACGGAAGTA	9972
rs758391340	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17626277	AATTCGCTAGAAAAT[-/A]AGATTTTTTATATAG	9972
rs758404316	snp	A/G	1.66457e-05	0.00288489	missense	NUP153	GRCh38.p7	6:17629494	ACACCAAATTTGAAG[A/G]ATGAGGAGGCTGCTG	9972
rs758438447	snp	C/T	1.70796e-05	0.00292224	missense	NUP153	GRCh38.p7	6:17637765	CTATCTTCGGCGATG[C/T]GAAACCTACAATGAA	9972
rs758514407	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17703673	AAAAAAAAAAAAGGA[C/G]AGTATTCTTTTGAAT	9972
rs758532466	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17630919	GAAGTACTTGACCTA[C/T]TGGCTCAAAACAAGG	9972
rs758537117	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698215	GGACTGATTGGATAG[A/G]GTAAACTTCGCTGCT	9972
rs758551332	snp	A/G	0.000250773	0.0111948	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706448	GGAGAGGCAGAGGCG[A/G]AGGCCTTAGAGAGCC	9972
rs758554188	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672255	GGATGGTCAAAAGTC[C/T]AGAAATAAAGCCATG	9972
rs758570901	snp	C/T	1.65045e-05	0.00287263	missense	NUP153	GRCh38.p7	6:17637696	AAAAGCTACTTATTG[C/T]TGGTCTTGTATAAAC	9972
rs758614648	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17616741	GGGCAAAATGATAGG[-/T]TTTTTTTGTTTGTTT	9972
rs758677495	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681722	ACATACACATAGGTT[A/G]AAATGTTTCCCAGGG	9972
rs758707361	snp	C/G	1.64751e-05	0.00287007	missense	NUP153	GRCh38.p7	6:17629027	AAGGAGCCACTGAAG[C/G]ACTCTTGGTTTCTAT	9972
rs758707630	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690488	GCCTCCTATTATTTA[C/T]AGTAATTATAATGAA	9972
rs758722235	snp	C/T	1.65173e-05	0.00287374	missense	NUP153	GRCh38.p7	6:17637186	AGGACACACACTTAT[C/T]GTCTTCTGCATTATT	9972
rs758727245	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677648	CCTTTGGTTCAGATC[C/T]CCTTTATGTCCCTCA	9972
rs758736844	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682437	TCGACTGACTATTCC[C/T]TTAACGAAAGATTTC	9972
rs758750428	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17659767	TGAGCCACCGTGCCC[A/C]GCCGCCAACCCGTTT	9972
rs758751877	snp	C/T	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17628945	GCAGGCTCCACGTTG[C/T]CAAAAGAGAATCCTC	9972
rs758759687	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17661565	GCTCTGGGTCTCTTC[A/G]AACCCCACCCCTACA	9972
rs758883489	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699366	CCAGGAATAATGGTG[C/T]GTGCTACTCCAGAGG	9972
rs758900054	snp	A/C	0.000155767	0.0088238	splice-acceptor-variant, intron-variant	NUP153	GRCh38.p7	6:17632845	CAGGTACTGAACTTC[A/C]TAAAAAAAAAAAAAA	9972
rs758903842	snp	A/G	1.80673e-05	0.00300555	missense	NUP153	GRCh38.p7	6:17646093	ATAATTGGTTCTAAA[A/G]TACTACTAGAACCAG	9972
rs758904884	in-del	-/AG			intron-variant	NUP153	GRCh38.p7	6:17694993	CAAGGAAAAAAAAAA[-/AG]AGAGAGTGGGAAGTA	9972
rs758923402	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618031	TCACAAAATACCGAG[C/T]GCTCCAGCCATCTTC	9972
rs758938817	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700208	AGATCCTAAATCAAA[C/T]AGTTCTATTTAATTT	9972
rs758941313	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695934	GAATGGCGTGAACCC[A/G]GAAGGCGGAGCTTGC	9972
rs758943685	snp	A/T	1.64789e-05	0.0028704	missense	NUP153	GRCh38.p7	6:17616168	AAGAAGAGAACACAT[A/T]TTTCCCATTTGACCT	9972
rs758954965	snp	C/T	4.62182e-05	0.00480697	intron-variant	NUP153	GRCh38.p7	6:17632894	GATTTCATGAAAATT[C/T]TAATTTACAGTATGT	9972
rs758968667	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17679915	GGAATGCGAAATAAC[G/T]GATTTACAGCATTGT	9972
rs759000752	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660082	AAGGAGGTCATAATT[C/T]TGGTGAGCTATAGTA	9972
rs759005760	snp	C/T	1.64925e-05	0.00287158	synonymous-codon	NUP153	GRCh38.p7	6:17669433	TTAAAAATTTACCGC[C/T]AAAGGGCTTGACATC	9972
rs759007962	snp	C/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17688546	TGCATACATCTTCAT[C/T]CTTGTTGAAGTATCT	9972
rs759024422	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17650586	ATAAATCACAGCTCA[A/T]TAAAATTGATCCAAA	9972
rs759048476	snp	C/T	1.68354e-05	0.00290128	intron-variant	NUP153	GRCh38.p7	6:17649141	AACAAATGTCACCTG[C/T]ATTTATATAATGGTT	9972
rs759064954	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17634980	AACAAATTAAAAAAT[-/AA]AAAAAAAAAATAAAT	9972
rs759067962	snp	C/G	1.64808e-05	0.00287057	synonymous-codon	NUP153	GRCh38.p7	6:17628776	AGAATTCTCATCTTT[C/G]GTTTGCTCTGAATTC	9972
rs759067990	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17665142	CCTTTATGTGTTATA[-/C]AGTTGCTAGAATACA	9972
rs759097829	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641562	AACAAACAAACAAAC[A/G]AACAAAAAGGCCAGG	9972
rs759111334	snp	A/G	3.32668e-05	0.00407827	intron-variant	NUP153	GRCh38.p7	6:17675812	AATATACAACTTAGA[A/G]CGATACACTACCACA	9972
rs759118330	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622261	TAGAGACCAGCCTGG[A/G]TAACATGGCAAAACC	9972
rs759121267	snp	A/C	1.73039e-05	0.00294137	intron-variant	NUP153	GRCh38.p7	6:17616520	TTTCAATAAAAAATT[A/C]TCTTACCCCACTGTA	9972
rs759148570	in-del	-/ACTCA			intron-variant	NUP153	GRCh38.p7	6:17634342	ATCTTGAGTGAACAC[-/ACTCA]ACTCTACTCTCATGA	9972
rs759185793	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661378	CGTATGTTTTACAAA[C/T]AGACAAAACTATACA	9972
rs759260258	snp	C/T	3.47096e-05	0.00416576	intron-variant	NUP153	GRCh38.p7	6:17668937	AACACAACAAAATTG[C/T]AGACAGTTTAAATAA	9972
rs759264273	in-del	-/TTTCA			intron-variant	NUP153	GRCh38.p7	6:17629756	TCCTGACAAGCCACT[-/TTTCA]TTTATCAGACTGGCT	9972
rs759269085	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690319	TGTGCAGTAAAATAA[C/T]TGCTTGAGAAAGCTT	9972
rs759278619	snp	A/C	1.79064e-05	0.00299214	intron-variant	NUP153	GRCh38.p7	6:17669045	TGAAAAAAAAAAAAA[A/C]CACTATTAGAATAGA	9972
rs759286324	snp	A/G	1.80997e-05	0.00300824	intron-variant	NUP153	GRCh38.p7	6:17637799	AGGAGAGAGTGCAAC[A/G]TTAGAGAAGCTTTAT	9972
rs759295538	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17661080	AGCACTTTGCAAGGC[A/C]GAGGCAGGTGGATCA	9972
rs759330205	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17618299	ACTCATAACAACTAC[A/G]GGTAGCCAAGGAGTA	9972
rs759330946	in-del	-/ACAC/ACACACAC			intron-variant	NUP153	GRCh38.p7	6:17693187	AGCTTTTTCCTACAC[-/ACAC/ACACACAC]ACACACACACACACA	9972
rs759339152	snp	A/G	1.65151e-05	0.00287355	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632661	TTACCTTTAAACCCA[A/G]ATTTTGTGCCTGGCT	9972
rs759357866	in-del	-/C	3.63098e-05	0.0042607	intron-variant	NUP153	GRCh38.p7	6:17632857	TCCTAAAAAAAAAAA[-/C]AAAAAACGGGGAGTG	9972
rs759363188	snp	A/C	1.64768e-05	0.00287021	missense	NUP153	GRCh38.p7	6:17661676	CCAGAGGTTTAGAAG[A/C]AACAAAGCGTGTTCT	9972
rs759369480	snp	C/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708192	GCCATGTTGGCCAGG[C/G]TGGCCTTGAACTCCT	9972
rs759386273	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17699834	GCTAGATTCTGTCTC[-/A]AAAAAAAAAGAAAAG	9972
rs759428257	snp	A/C	1.64923e-05	0.00287156	missense	NUP153	GRCh38.p7	6:17675721	CCGATGAAGAGAAGG[A/C]CTTGTTAACACATCT	9972
rs759453309	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17627731	TTTCACTTTAAGGGC[A/C]CTGTTGTTTTTAGCA	9972
rs759463868	in-del	-/AAG	7.21774e-05	0.00600695	intron-variant	NUP153	GRCh38.p7	6:17626202	CAAACATAAATCCTT[-/AAG]AATAGTCTCAGAAAG	9972
rs759486108	snp	C/T	1.6646e-05	0.00288491	intron-variant	NUP153	GRCh38.p7	6:17669570	TAAACCCTATATTAT[C/T]TGTTGCAACATAAAA	9972
rs759487748	snp	C/T	3.30322e-05	0.00406387	synonymous-codon	NUP153	GRCh38.p7	6:17674914	ACCTACCTGATAAGG[C/T]GTATTTCGTAGTTTA	9972
rs759487977	snp	A/G	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637278	CCTAAGGTACCAGTG[A/G]TTACAGTGCAGCTGG	9972
rs759517429	in-del	-/TTC	4.94344e-05	0.00497139	cds-indel	NUP153	GRCh38.p7	6:17628977	TTTGGTGGCAGGCAT[-/TTC]TTCTTTTTTAGCTTC	9972
rs759529094	in-del	-/GG	4.95013e-05	0.00497475	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616052	CAGTATCTGAAAGCA[-/GG]GCACCAGCTGTTGTT	9972
rs759543070	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17625726	TTTTGTGATAACCTG[C/T]TATATGATATTCGCT	9972
rs759580531	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664815	CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGTGGG	9972
rs759609606	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	NUP153	GRCh38.p7	6:17624706	TGTGGAAGATGATAT[A/G]GATCCAAAGCCTGGG	9972
rs759616457	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17626408	GGCCTTTGGCATTCA[A/G]GTTAATAAAAATACA	9972
rs759625731	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17638376	TTTGTCTTACACACA[A/C]CACCACCATCTGTGA	9972
rs759695761	snp	C/T	3.29538e-05	0.00405904	missense	NUP153	GRCh38.p7	6:17629084	TCTCAGAGGTCACTA[C/T]GGTGTTAGCAGGAGC	9972
rs759739031	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17637001	TAAAGATCTAGCTGC[A/T]AACAAGACATTTTTA	9972
rs759751500	snp	G/T	2.20446e-05	0.00331991	intron-variant	NUP153	GRCh38.p7	6:17646063	GTAAGAAATTTTTAC[G/T]TACCTGAACTACTTA	9972
rs759791413	snp	A/G	5.75948e-05	0.00536601	intron-variant	NUP153	GRCh38.p7	6:17646164	TCCAATCTGTAAAGA[A/G]AAAGAATATCCTTAT	9972
rs759793446	in-del	-/GA	7.1426e-05	0.00597561	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706232	CCGTCCCCTCCAGCC[-/GA]GTTTCCCCACCCGCC	9972
rs759800251	snp	C/G	1.64857e-05	0.00287099	missense	NUP153	GRCh38.p7	6:17626008	GCAGAGCTGCTCACA[C/G]GATTGCTGGACTGTC	9972
rs759802312	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643960	ATCCTCTTGAATTAA[C/T]AGTTAACATTAAAGA	9972
rs759807567	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17663483	TGCCTGGGCTAGTCT[C/T]GAATTCCTGGACTCA	9972
rs759809742	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676910	CTATATCAAGACCAC[C/T]TAAGCCTTACGCAGC	9972
rs759819330	snp	C/T	3.29478e-05	0.00405867	synonymous-codon	NUP153	GRCh38.p7	6:17688535	TGTTGAACAGCTGCA[C/T]ACATCTTCATTCTTG	9972
rs759824939	in-del	-/GAG	9.97307e-05	0.00706084	cds-indel	NUP153	GRCh38.p7	6:17669301	AACTTACAGAATTCA[-/GAG]GAGAAGAAACAATGG	9972
rs759828548	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17659980	AAGGAAAGACAGAGC[C/G]TCCAGACCAGCAATA	9972
rs759847131	snp	C/T	1.64985e-05	0.0028721	missense	NUP153	GRCh38.p7	6:17688609	ATTCTGTAACCCTGC[C/T]AAGAATGCCCTGTTG	9972
rs759854627	snp	C/T	1.64814e-05	0.00287061	missense	NUP153	GRCh38.p7	6:17665318	TTAAAATAAACACTT[C/T]GATTTGTTGCTATGG	9972
rs759930405	snp	C/T	2.86808e-05	0.00378677	synonymous-codon	NUP153	GRCh38.p7	6:17628671	AGCTGTAGTACTAGT[C/T]TGAGCTCCAAAGGCA	9972
rs759943333	snp	A/C			missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632738	CACTAGGCACAATTC[A/C]CAGTCCCAGCTTCCC	9972
rs760018701	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642977	GAATAAGTCAATCCA[C/T]AGAGACAGAACACAA	9972
rs760032451	snp	A/G	1.67739e-05	0.00289597	intron-variant	NUP153	GRCh38.p7	6:17675386	GAAACAAAATTACAT[A/G]ATCCATAGTAATAAC	9972
rs760036221	in-del	-/AATAT	1.71399e-05	0.0029274	intron-variant	NUP153	GRCh38.p7	6:17665221	TCAAAGACTGGTAGA[-/AATAT]AATATACATATACTC	9972
rs760050946	snp	A/G	1.64819e-05	0.00287066	missense	NUP153	GRCh38.p7	6:17675587	TCATCATGCTGAGAG[A/G]TAGAATCTTTAATTT	9972
rs760054409	snp	A/C	0.00011597	0.0076139	missense	NUP153	GRCh38.p7	6:17626113	GCTGGTGTACTTGAA[A/C]TAGAGGAACTGTTGT	9972
rs760087570	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17689644	TGGGTTCAATGGATT[-/C]TCCTGCCTCAGCCTC	9972
rs760089904	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17685623	AAAATCTGTATTCCC[-/T]TAGTGACATCATAGC	9972
rs760113449	in-del	-/C	1.83791e-05	0.00303137	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706465	GGCCTTAGAGAGCCT[-/C]CCCCGCCGCCCGGCC	9972
rs760172554	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17683119	CCCTCAAAGTTATCC[A/T]TGGGGGCTGGAATCA	9972
rs760190832	snp	C/T	3.30006e-05	0.00406192	missense	NUP153	GRCh38.p7	6:17629420	ATCCTCCCTGATCTC[C/T]AAATTTAAAATTTCC	9972
rs760201967	snp	A/G			missense	NUP153	GRCh38.p7	6:17649203	TTGATGGGTGATGGA[A/G]AGGAAGTTGTGATCT	9972
rs760223730	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701842	TGTCTCGGGGGGGGG[A/G]GGAAAAAAGCTAAAT	9972
rs760229801	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684900	TACTGATTAAGTTCA[C/T]CATCTTATATGGGTG	9972
rs760235425	snp	A/G	0.000231723	0.0107614	intron-variant	NUP153	GRCh38.p7	6:17628635	AATAATAATAATAAT[A/G]ATAAAAAGTTAATAC	9972
rs760244008	in-del	-/AAA			intron-variant	NUP153	GRCh38.p7	6:17623358	AACTGAAAAATGGCC[-/AAA]AAAAAAAAAAAAAAA	9972
rs760268398	snp	A/T			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632579	GAAGCTGTTCTCAAA[A/T]ACTTCATTTTTAAAT	9972
rs760304403	snp	G/T	1.67885e-05	0.00289724	missense	NUP153	GRCh38.p7	6:17637749	TGAGCAGCAACAGAA[G/T]CTATCTTCGGCGATG	9972
rs760306174	in-del	-/T	7.1053e-05	0.00595999	intron-variant	NUP153	GRCh38.p7	6:17628625	TAAAAAAAAAAATAA[-/T]AATAATAATAATAAA	9972
rs760323024	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17639201	TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGAACT	9972
rs760331875	in-del	-/TAAT			intron-variant	NUP153	GRCh38.p7	6:17628622	TTGTAAAAAAAAAAA[-/TAAT]AATAATAATAATAAA	9972
rs760357295	snp	A/G	1.75265e-05	0.00296023	intron-variant	NUP153	GRCh38.p7	6:17637786	CTACAATGAACGAAG[A/G]AGAGAGTGCAACGTT	9972
rs760387479	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17641373	AACCCCATCTCCACT[A/T]AAAATACAAAAAGTA	9972
rs760392087	snp	C/T	1.64817e-05	0.00287064	missense	NUP153	GRCh38.p7	6:17637671	TCCCCAAACCCAATT[C/T]CACTAGAAGAAAAGC	9972
rs760414084	snp	A/T	1.64742e-05	0.00286999	synonymous-codon	NUP153	GRCh38.p7	6:17624697	AAATAATGCTGTGGA[A/T]GATGATATAGATCCA	9972
rs760415393	snp	C/T	3.29717e-05	0.00406015	missense	NUP153	GRCh38.p7	6:17675704	GAAAAATTCAGATGG[C/T]TCCGATGAAGAGAAG	9972
rs760426629	snp	C/T	1.6516e-05	0.00287362	intron-variant	NUP153	GRCh38.p7	6:17661644	GAGTATATGAGTATA[C/T]AACCCTACCTCCTCC	9972
rs760463147	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17638663	TTTTCAGATTTTCCT[A/C]ATTTCAGTCAAATGA	9972
rs760494616	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	NUP153	GRCh38.p7	6:17624592	TCCAGAGCCAAATGC[A/G]GACTGACTAGGTTGC	9972
rs760505036	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639208	TCAGCCTCCCGAGTA[A/G]CTGGAACTACAGGTG	9972
rs760509626	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679770	CTAACCCTGAGGCTT[C/T]AGTCACAAAAAGAAA	9972
rs760531805	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17655950	TGGTTCAACCCTGCA[A/G]TCCCAGCCCTTTGGG	9972
rs760536760	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17653522	GCTCCTTAGAAAGTT[-/A]AACATACAACTTAGC	9972
rs760537389	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17650486	TTCAGCTGCTGCCTA[A/C]CACAGGGGAGACAGA	9972
rs760558718	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17626831	TTGTCAAGCTCTACA[A/G]AAATTCCCCTAAGAA	9972
rs760620516	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	NUP153	GRCh38.p7	6:17688514	GCGTGGAACCTCGCT[C/T]GTGTCTGTTGAACAG	9972
rs760623204	snp	C/T	0.000384615	0.0138622	missense, intron-variant	NUP153	GRCh38.p7	6:17651911	TCAGCTTGGGCAATA[C/T]GGTGAGACCTTGTCT	9972
rs760628851	snp	C/T	0.000195899	0.009895	missense	NUP153	GRCh38.p7	6:17646136	TTTTTGCAACAGGCA[C/T]ACTAAATGTAAATCC	9972
rs760676848	snp	A/C	1.66101e-05	0.0028818	intron-variant	NUP153	GRCh38.p7	6:17669559	TGCCTGTAAAGTAAA[A/C]CCTATATTATTTGTT	9972
rs760683096	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17690210	ACAAAAAATTAGCCA[C/G]GCGTGGTGGCGGGCG	9972
rs760685825	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17635835	TCCTCTGCTGAAAAT[A/G]ATGGTTCATCATTGA	9972
rs760788292	in-del	-/CTTTT			intron-variant	NUP153	GRCh38.p7	6:17618562	GAAGTTAAAATCTCT[-/CTTTT]TTTTTTTTTTTTTTT	9972
rs760801493	in-del	-/T	1.65534e-05	0.00287688	intron-variant	NUP153	GRCh38.p7	6:17661634	TAAACCTCAAGAGTA[-/T]ATGAGTATACAACCC	9972
rs760810361	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633813	CCTAACTGATCTCTA[C/T]ATTTTATAGGTATGT	9972
rs760820564	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17663330	GCAGTGGTGCTATCA[C/T]AGTTCACTTTAGCCT	9972
rs760836284	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690486	CTGCCTCCTATTATT[C/T]ATAGTAATTATAATG	9972
rs760850709	snp	A/G	3.29516e-05	0.00405891	missense	NUP153	GRCh38.p7	6:17628912	CCCAAAACAAACACT[A/G]AGGCAGATGGCAGAG	9972
rs760878651	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17685316	ACTTTGGGAGGCTGA[A/G]GAAGGTGGATCATGA	9972
rs760892299	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17692596	ACCAGTATGAAGGAA[A/C]AAACATCCTTGTGTT	9972
rs760895542	snp	C/T	1.65921e-05	0.00288024	missense	NUP153	GRCh38.p7	6:17629353	TTAGAAAATTTAAAG[C/T]CTTCACTCATGGGGT	9972
rs760941892	snp	C/T	1.64817e-05	0.00287064	synonymous-codon	NUP153	GRCh38.p7	6:17625959	AGAAAATAGCAAAGA[C/T]TGAGAGGTGCTGGAT	9972
rs760953532	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	NUP153	GRCh38.p7	6:17688439	TGTGATTCTCCCATC[A/G]GTAATATTAGAGCTC	9972
rs760982725	snp	A/G	1.65897e-05	0.00288003	missense	NUP153	GRCh38.p7	6:17675362	GTGTTCTTTGAAACA[A/G]TTATATCTGAAACAA	9972
rs761003620	snp	A/G/T	5.32911e-05	0.00516171	intron-variant	NUP153	GRCh38.p7	6:17646047	GTTTGTATGTTAAAA[A/G/T]GTAAGAAATTTTTAC	9972
rs761005555	in-del	-/ACT	1.89013e-05	0.00307413	intron-variant	NUP153	GRCh38.p7	6:17669047	AAAAAAAAAAAAAAC[-/ACT]ATTAGAATAGATGGG	9972
rs761010553	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17659482	TTTGTTTTTGTTTTG[-/T]TTTGTTTTTGAGACA	9972
rs761035719	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671079	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA	9972
rs761091088	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17647448	TCTGGGGATAATGGG[A/G]AAATCTGAATATGGA	9972
rs761098732	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641715	AACAAATTAGCCGGG[C/T]GTGGTGGCAGGCGCC	9972
rs761151966	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642829	AACTGTGGCACATCA[A/G]TACAATGGAATATTA	9972
rs761158790	snp	A/G	0.000135197	0.00822071	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706346	CCGCGTCCGGATCTT[A/G]CCGCCACCGCCCCCT	9972
rs761175013	snp	A/G	4.32545e-05	0.00465031	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706410	CCTCCGCCGCTTCCC[A/G]CTCCGGGGCGGGTAA	9972
rs761177025	snp	G/T	1.6486e-05	0.00287102	synonymous-codon	NUP153	GRCh38.p7	6:17675247	GGAAAGTGTTCCAAA[G/T]GCAGACAAGTTGAAT	9972
rs761188085	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17631561	CTGAGTACACTTTAT[G/T]TAGCTACAACTTATA	9972
rs761204627	in-del	-/AAGA			intron-variant	NUP153	GRCh38.p7	6:17687528	TAGTTGAACATTACT[-/AAGA]AAAATTAGGTTTGCC	9972
rs761205652	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17669615	TTCATGCAGTGAAAA[-/T]ATTTACAAGATAGAA	9972
rs761216829	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17642621	CTACTGTGGAAAACA[G/T]TTTAGTGATTCTTCA	9972
rs761230401	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692510	CAGAGACCCTGTTTC[C/T]AAAAACAAAAAGACA	9972
rs761235244	in-del	-/AAAG			intron-variant	NUP153	GRCh38.p7	6:17622704	ACATAAAAAAAAAAT[-/AAAG]AGAGGAAGTCAATAA	9972
rs761249845	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	NUP153	GRCh38.p7	6:17649223	AGTTGTGATCTCAGG[A/G]GAACTAAAATTAAAG	9972
rs761250065	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17703986	GATTTTTATTTTATC[C/T]AAGTACATTTAAGCT	9972
rs761272871	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619040	CACTCCCTACACAAA[C/T]GATAAAAACAAACCC	9972
rs761279822	snp	G/T	1.65518e-05	0.00287674	missense	NUP153	GRCh38.p7	6:17629210	CCCCAAATTGAAATG[G/T]AGTTAAAGAAACTGG	9972
rs761310195	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653316	CAATGAGCACATAAA[A/G]AAGAACACAATACTA	9972
rs761310886	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682551	TTTATCAACTAAGTT[C/T]ATGTAATATTCTAAA	9972
rs761337001	snp	C/G	1.64822e-05	0.00287068	missense	NUP153	GRCh38.p7	6:17675594	GCTGAGAGGTAGAAT[C/G]TTTAATTTCCTTTAC	9972
rs761341217	snp	A/C	3.34035e-05	0.00408664	missense	NUP153	GRCh38.p7	6:17637744	TGGGCTGAGCAGCAA[A/C]AGAATCTATCTTCGG	9972
rs761398219	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17630109	CAAGGTAAAAGGAAG[A/T]AAGAATATATAGGGG	9972
rs761415082	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	NUP153	GRCh38.p7	6:17637655	CCCAGCTTTTAAACT[C/T]TCCCCAAACCCAATT	9972
rs761417354	in-del	-/TCCAAATACAAA	1.9042e-05	0.00308555	cds-indel	NUP153	GRCh38.p7	6:17624814	TGCTGAGGGTCCAGT[-/TCCAAATACAAA]GGAGGATCCTGGAGG	9972
rs761463643	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641610	TGTAATCCCAGCATT[C/T]TGGGAGGCTGAGGCA	9972
rs761501796	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17682096	GCTCTTGTAGTCCCA[A/G]CTACCTGGGAGAGTG	9972
rs761517062	snp	A/G	1.64762e-05	0.00287016	missense	NUP153	GRCh38.p7	6:17628997	CTTTTTTAGCTTCTG[A/G]TGTCTTACATGTGAA	9972
rs761519212	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678233	TGGTGGCACACGCCT[A/G]TAATTCCAGCTACCT	9972
rs761520777	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17693342	CTGCCCCATGAGAGA[G/T]ATTAAACACTAGATA	9972
rs761540473	snp	A/G	2.5975e-05	0.00360373	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706426	CTCCGGGGCGGGTAA[A/G]GGGGCGGGAGAGGCA	9972
rs761543163	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17635102	GCACAGCTTGGCTTA[-/TT]TCTTTTTTTTTTTTT	9972
rs761575557	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17644390	AATCATTCAACATCT[-/C]CCTAATGCAGTCAGA	9972
rs761600273	snp	A/G	1.65466e-05	0.00287628	missense	NUP153	GRCh38.p7	6:17616692	CCAAACTGGAAAGCC[A/G]AACCTGCAATAGTTA	9972
rs761618943	snp	A/C	3.29495e-05	0.00405877	missense	NUP153	GRCh38.p7	6:17628904	CTGTCCTTCCCAAAA[A/C]AAACACTGAGGCAGA	9972
rs761725847	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648251	AGCACTTTGGGAAGC[C/T]ATGACAGAGGGAATT	9972
rs761751293	snp	C/G	1.65466e-05	0.00287628	intron-variant	NUP153	GRCh38.p7	6:17669384	ATTTTTCAATAATAT[C/G]AAGTTTTGTTACACT	9972
rs761771913	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17641463	TGCTTGAACCTGGGA[-/G]GGCGGAGGTTGCAGT	9972
rs761774741	in-del	-/AT			intron-variant	NUP153	GRCh38.p7	6:17655825	ATTTGTGGTCTCAAC[-/AT]ATCTGACTTCTGATG	9972
rs761815700	snp	A/G	3.29881e-05	0.00406115	synonymous-codon, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632801	GCCTCCAGAAGGCAG[A/G]GAGACAGGTACAGTG	9972
rs761840614	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698514	GAGGCCGAGGTGGGC[A/G]GATCACAAGGTCAGG	9972
rs761849492	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17634773	TGACTTCAGCAGCTT[C/G]AAATCAACGTCTTTA	9972
rs761857620	snp	A/G	1.65023e-05	0.00287244	synonymous-codon	NUP153	GRCh38.p7	6:17625830	GCTAGATGTGGTTGT[A/G]GCTCCAAAGCCGAAA	9972
rs761859686	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17644947	AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT	9972
rs761862545	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17676917	AAGACCACCTAAGCC[A/T]TACGCAGCAGCTGCT	9972
rs761891912	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17688065	CGGAGCTTGCAGTGA[C/G]CAGAGATCACACCCT	9972
rs761914196	snp	A/T	3.54434e-05	0.00420957	intron-variant	NUP153	GRCh38.p7	6:17665197	TAGTCTTACTTATTC[A/T]AATCAATATTCAAAG	9972
rs761937441	in-del	-/CACACACC/CACACC			intron-variant	NUP153	GRCh38.p7	6:17693216	ACACACACACACACA[-/CACACACC/CACACC]CTTATAAAATCACAG	9972
rs761958338	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17674298	AAATACTCTAAAACA[A/T]TGAAAAATTGTAGTA	9972
rs761974864	in-del	-/TA			intron-variant	NUP153	GRCh38.p7	6:17660596	ACATATAAGAAATTA[-/TA]TATATATATCCCTAC	9972
rs762006944	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17695644	ATGCACAGCCAACTA[C/T]AAGACATTAGAAATT	9972
rs762009802	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656752	TGTTTATTAGGAAAG[C/G]TTTAGGGGGTAGATT	9972
rs762024425	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17692441	ATCACTTGAGCCTAG[C/G]AATTCAAGGTTGCAG	9972
rs762032185	snp	A/C	3.29674e-05	0.00405988	synonymous-codon	NUP153	GRCh38.p7	6:17674944	AGACTGTCTTACAGC[A/C]GCTGCTGCCCCACCG	9972
rs762062109	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17696228	TTTTTAAAAGAGTTT[G/T]GAAGTACTAAAGACT	9972
rs762062312	snp	G/T	1.64991e-05	0.00287215	missense	NUP153	GRCh38.p7	6:17675233	TTAGTACTCACAGGG[G/T]AAAGTGTTCCAAAGG	9972
rs762094081	snp	A/T	1.64993e-05	0.00287218	intron-variant	NUP153	GRCh38.p7	6:17661972	TTAAATACAGACCTT[A/T]CAAGTTAAATATAAA	9972
rs762104821	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698716	ACACTCCAGCTTGGG[C/T]GACAGAGCAAGACTC	9972
rs762109939	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17640874	GTGATCCTCCCACAT[C/T]GGCCTCCCAAAGCAC	9972
rs762123646	snp	C/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637381	CAGGTTTCGGTGTTT[C/G]ACAGGCTACACATTT	9972
rs762142682	in-del	-/TTT			intron-variant	NUP153	GRCh38.p7	6:17668070	TTTAGTTTACTGAAC[-/TTT]TTTTTTTTTTTTTTT	9972
rs762162026	snp	C/T	3.00458e-05	0.00387582	intron-variant	NUP153	GRCh38.p7	6:17624860	AAGAAACACTTAAGT[C/T]ACCATGGTGGCTAAT	9972
rs762179852	in-del	-/T	1.98541e-05	0.00315066	intron-variant	NUP153	GRCh38.p7	6:17632870	AAAAAAAACGGGGAG[-/T]TGGGGGGAGATTTCA	9972
rs762188635	snp	A/C	1.67806e-05	0.00289656	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706331	CCCCTGGTGGCAACG[A/C]CGCGTCCGGATCTTG	9972
rs762207363	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17659836	AAATTGGTTTGCTAC[-/A]AAACCTATAAAATTT	9972
rs762230644	snp	A/G	1.6922e-05	0.00290873	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706268	CACCGCGGCGTCGGG[A/G]TCCCATACCTGATGC	9972
rs762235053	snp	A/G	3.70007e-05	0.00430105	intron-variant	NUP153	GRCh38.p7	6:17616491	CACATACCCTTACCA[A/G]TGTAACTTCTCCATT	9972
rs762241462	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17663207	AAATCTGTAGAAGTC[C/T]AATATTATGCTAAAA	9972
rs762256796	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17647214	TTAAAATAATATAAA[C/G]ATGCCAAATCTGGGG	9972
rs762269189	in-del	-/AT			intron-variant	NUP153	GRCh38.p7	6:17663254	CACACACACACACAC[-/AT]ACACACATATATATA	9972
rs762271605	snp	C/T	1.69e-05	0.00290684	intron-variant	NUP153	GRCh38.p7	6:17649138	AAGAACAAATGTCAC[C/T]TGTATTTATATAATG	9972
rs762350685	snp	C/T	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637312	ATGAAGCAGTCATAG[C/T]CTCAGCACTTTCCGA	9972
rs762372758	snp	C/T	3.29489e-05	0.00405874	missense	NUP153	GRCh38.p7	6:17647845	CCTCAGTAGATTTTA[C/T]GATTGGAGATGAAAA	9972
rs762375642	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17644345	CACACTGCTATCACT[A/G]TACTCACATCCATCT	9972
rs762382473	snp	A/C	5.32704e-05	0.00516065	intron-variant	NUP153	GRCh38.p7	6:17669041	AGGCTGAAAAAAAAA[A/C]AAAACACTATTAGAA	9972
rs762408024	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17680693	TCCACAAATTATATA[G/T]GTGATAAGGGATTAA	9972
rs762415907	snp	A/C/G	4.94273e-05	0.00497108	missense	NUP153	GRCh38.p7	6:17629018	TACATGTGAAAGGAG[A/C/G]CACTGAAGCACTCTT	9972
rs762438217	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17622771	GTTATAGTATACCAT[A/T]TGGCTCAGCAATAAT	9972
rs762456656	snp	C/G	1.6904e-05	0.00290719	intron-variant	NUP153	GRCh38.p7	6:17649338	ATATATTTCATCTTT[C/G]ACATCATTCTTTTAT	9972
rs762457655	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17702518	TCTCAAAAACAAAAC[-/A]AAAAAAAATCAGCCG	9972
rs762466088	snp	C/T	1.64765e-05	0.00287019	missense	NUP153	GRCh38.p7	6:17616107	GACCTTTATTTCCTG[C/T]GTCTAACAGCAGTCT	9972
rs762481848	snp	C/T	3.31066e-05	0.00406844	intron-variant	NUP153	GRCh38.p7	6:17669378	ATTAAGATTTTTCAA[C/T]AATATCAAGTTTTGT	9972
rs762540513	snp	C/T	1.65809e-05	0.00287926	missense	NUP153	GRCh38.p7	6:17629363	TAAAGCCTTCACTCA[C/T]GGGGTTTATAGACCC	9972
rs762561986	snp	C/T	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17649258	GCAGTGAAGAACTGG[C/T]GATCGGTAGAGAGAT	9972
rs762568353	snp	A/C	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17637645	GCCATGATGACCCAG[A/C]TTTTAAACTCTCCCC	9972
rs762577185	snp	A/G	4.69142e-05	0.00484303	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706418	GCTTCCCGCTCCGGG[A/G]CGGGTAAGGGGGCGG	9972
rs762589361	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666951	ACAACTCAATAAGAG[A/G]GTCTATTTTGTAGAC	9972
rs762592934	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17691213	TCTTCCATGTATTGT[G/T]CAAATTTTCAATAGA	9972
rs762612484	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17678093	GGGCACAGTGGTTCA[C/T]ACCTGTAATCCCAGC	9972
rs762613733	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17677621	CCCAACACTGCTTTC[C/T]TACCCACCTTTCCTT	9972
rs762652151	snp	A/C	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17628878	AGTGACAGGCTCTTG[A/C]TGTTTCTCTTCTGTC	9972
rs762654276	snp	C/T	1.6534e-05	0.00287519	missense	NUP153	GRCh38.p7	6:17616566	TGGTTAAATGGAAAG[C/T]CCCCCGAGCCTGAAG	9972
rs762655688	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17622456	TGCGGCAAGGTGAGA[A/C]CCTGTCTCAAAAAAT	9972
rs762663043	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17702401	TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGCAGA	9972
rs762685055	snp	C/T	1.64762e-05	0.00287016	missense	NUP153	GRCh38.p7	6:17688429	CTGGCTCAGGTGTGA[C/T]TCTCCCATCAGTAAT	9972
rs762713832	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679960	CCACTACTCAAGGTA[A/G]TCATCGCAACCAGAT	9972
rs762715927	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17623476	CAGAATCCATCAGGA[A/G]AAGTTTTTATTATCT	9972
rs762726909	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680349	ATTTCAAGACCACTC[A/G]ATGGGAAAAGGACAG	9972
rs762738314	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17675994	TAAACCAGTAAGAGT[A/G]ATGTGATACGATACA	9972
rs762745993	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	NUP153	GRCh38.p7	6:17628797	CTCTGAATTCCCAAA[A/G]GAAAACACTGGTTGA	9972
rs762761006	snp	A/T	0.000148372	0.00861184	synonymous-codon, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632789	CAATCCTAGAGAGCC[A/T]CCAGAAGGCAGAGAG	9972
rs762783745	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17658702	GTCTCACAAGCTGAG[G/T]GAAAATTTAAAAAAT	9972
rs762788302	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696556	GTCAGGAGATCGAGA[C/T]CATCCTGGCTAACAC	9972
rs762804259	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656162	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCACC	9972
rs762839818	snp	C/T	3.29826e-05	0.00406082	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632675	AGATTTTGTGCCTGG[C/T]TTTGCACTTTCACAT	9972
rs762872103	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17635436	GACAGGGTCTCACTC[-/T]TGTCACCCAGGCTGA	9972
rs762881007	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17623360	CTGAAAAATGGCCAA[-/A]AAAAAAAAAAAAAAA	9972
rs762894869	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17683192	CCTGTAAATCACAAA[C/T]GGTTTTTCTCCCCCA	9972
rs762932818	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17618453	TAATGAATACTTCAT[A/C]CACTGGAGAGTTGGG	9972
rs762975092	snp	C/G	5.21281e-05	0.00510503	intron-variant	NUP153	GRCh38.p7	6:17624847	TCCTGGAGGCCCAAA[C/G]AAACACTTAAGTCAC	9972
rs762988636	snp	A/G	1.64836e-05	0.0028708	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17640015	ACCCTCACAATCTTC[A/G]GGTGGTGTCTTCTTA	9972
rs762992173	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17655600	CTGGGATTACATGTG[C/G]CCGCCATCACACCCG	9972
rs762992419	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697570	CAGGCACCTGTAATC[C/T]CAGCTACTTGAGAGG	9972
rs763010279	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17668070	TTTAGTTTACTGAAC[-/T]TTTTTTTTTTTTTTT	9972
rs763037097	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17618721	CAGGCGCCCGCCACC[A/T]CGCCTGGCTAATTTT	9972
rs763039385	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17617011	CACCTCGGCCTCCCA[A/C]AGTGCTGGATTACAG	9972
rs763041659	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695601	TTGATTTCCACCGTT[A/G]AAGACTTACACAGAA	9972
rs763068060	snp	A/G	6.58989e-05	0.00573978	missense	NUP153	GRCh38.p7	6:17624722	GATCCAAAGCCTGGG[A/G]GATTGGGCTGGCTGG	9972
rs763086883	snp	G/T	1.67607e-05	0.00289483	intron-variant	NUP153	GRCh38.p7	6:17661817	AAACAACTGATATAT[G/T]ATTGTGGTCCATAAC	9972
rs763100159	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684401	GCTTCCAGCTTTTCT[C/T]CTGCAGCTTTATCAT	9972
rs763100352	in-del	-/AGACACTCA	0.000112167	0.00748806	intron-variant	NUP153	GRCh38.p7	6:17629566	TAAAAGACACCACAT[-/AGACACTCA]ATGTACTGATCCTCT	9972
rs763144906	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666375	TAAAAATTAGCCAGG[C/T]GTGGTGGCATGCGCC	9972
rs763152117	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706049	CCCCTGACCCAGAGA[A/G]TTGGGGGAAAGGCGG	9972
rs763205202	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707762	ATTAGAAAGGTCCTG[A/G]TGATCACATAGTCCA	9972
rs763229577	snp	C/G	1.72231e-05	0.0029345	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706260	CGCCAGGCCACCGCG[C/G]CGTCGGGGTCCCATA	9972
rs763230597	snp	C/T	6.58903e-05	0.00573941	synonymous-codon	NUP153	GRCh38.p7	6:17637373	ACAAGTTCCAGGTTT[C/T]GGTGTTTCACAGGCT	9972
rs763238334	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634581	AGCTGGGATTACGGG[C/T]ATCCACGACCACGCC	9972
rs763246594	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650803	ATATAAAGCAAAAAG[C/T]ACACATTGAATTTAC	9972
rs763272074	in-del	-/AAAAC			intron-variant	NUP153	GRCh38.p7	6:17658401	ACTGTCTCAAAACAG[-/AAAAC]AAAACAAAACAAAAC	9972
rs763275697	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17686598	GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT	9972
rs763279061	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17688628	AATGCCCTGTTGAGA[A/G]AAAAAACATATTATG	9972
rs763280033	snp	G/T	1.65015e-05	0.00287237	synonymous-codon	NUP153	GRCh38.p7	6:17674922	GATAAGGTGTATTTC[G/T]TAGTTTAGACTGTCT	9972
rs763302140	snp	A/G	1.64781e-05	0.00287033	missense	NUP153	GRCh38.p7	6:17629096	CTATGGTGTTAGCAG[A/G]AGCAGGGGTGGAGTT	9972
rs763323626	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17626702	CTGTTTTAATTATTA[C/T]AACTTTATACCATGG	9972
rs763324422	snp	C/T	6.58903e-05	0.00573941	missense	NUP153	GRCh38.p7	6:17637290	GTGGTTACAGTGCAG[C/T]TGGAAGATGAAGCAG	9972
rs763364231	in-del	-/CAAC			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705897	AAGTATAAGGGCCAT[-/CAAC]CAACCACATCTTTTC	9972
rs763370708	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674202	GATACATAAGGTAAC[A/G]TTTTGGGGTGATGAA	9972
rs763425299	snp	A/G	1.76319e-05	0.00296911	intron-variant	NUP153	GRCh38.p7	6:17665431	ATTTTCATATAAATC[A/G]ATGATTCATATCTAA	9972
rs763426217	snp	A/G/T	3.29717e-05	0.00406015	intron-variant	NUP153	GRCh38.p7	6:17662002	AGAAGTATAGCTGTA[A/G/T]AAGAAATGACAGTAC	9972
rs763441843	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17657115	AAGTTCTGAGATCTT[C/T]GGCTGAAGCTCAGGT	9972
rs763448251	in-del	-/AATA	1.66402e-05	0.00288441	intron-variant	NUP153	GRCh38.p7	6:17669567	AGTAAACCCTATATT[-/AATA]ATTTGTTGCAACATA	9972
rs763466458	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17700133	CAGAGACAATATGAA[A/G]ACCCTAAATCAGGAG	9972
rs763482788	snp	G/T	2.41543e-05	0.00347514	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706420	TTCCCGCTCCGGGGC[G/T]GGTAAGGGGGCGGGA	9972
rs763484040	snp	A/G	1.64792e-05	0.00287042	missense	NUP153	GRCh38.p7	6:17665327	ACACTTCGATTTGTT[A/G]CTATGGAAACTGGCT	9972
rs763503344	in-del	-/CCG	6.19662e-05	0.0055659	cds-indel, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706408	AGCCTCCGCCGCTTC[-/CCG]CTCCGGGGCGGGTAA	9972
rs763523045	in-del	-/CTTTT			intron-variant	NUP153	GRCh38.p7	6:17622093	GACTTTGTAGCATGG[-/CTTTT]CTTTTGTTTTGTTTT	9972
rs763572338	snp	A/G	1.68428e-05	0.00290192	intron-variant	NUP153	GRCh38.p7	6:17675397	ACATAATCCATAGTA[A/G]TAACACCAATACAAG	9972
rs763586860	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17629965	TTAAAGATAAACTCA[C/T]AGACATGCAAAATGC	9972
rs763590579	snp	C/T			missense	NUP153	GRCh38.p7	6:17669470	AAAGACTGCAATATT[C/T]GCCGAGCTGTTGAAC	9972
rs763614011	snp	C/T	1.65548e-05	0.002877	missense	NUP153	GRCh38.p7	6:17626108	AAGTGGCTGGTGTAC[C/T]TGAACTAGAGGAACT	9972
rs763629207	snp	A/G	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17675276	ATGCTGGTTTTTTTG[A/G]GCTGGTGGCAGTGTG	9972
rs763643125	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17652209	AATACTATCAGCTTA[C/G]TTCTACAGATCACTA	9972
rs763659311	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17677987	TAATTACATTCTTAA[G/T]ATCTAGAAGTGGTGG	9972
rs763677562	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17622596	TCTAATTTTTAGGGC[A/C]TCTGTAGCCTTTTCT	9972
rs763703321	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17679986	CAGATATGCTGCCTT[C/G]CGTACCCTACCCTGC	9972
rs763744926	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17620287	TATATGAGACTGGTA[-/T]AAAAAGACACATAGA	9972
rs763750668	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17696621	TTAGCTGGGTGTGGT[C/G]GTGGATGCCTGTAGT	9972
rs763756223	snp	C/G	5.14275e-05	0.00507061	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706363	CGCCACCGCCCCCTC[C/G]GACTCCTCCGGCTCC	9972
rs763756875	snp	C/T	1.64751e-05	0.00287007	missense	NUP153	GRCh38.p7	6:17637653	GACCCAGCTTTTAAA[C/T]TCTCCCCAAACCCAA	9972
rs763758911	snp	A/T	1.65712e-05	0.00287843	synonymous-codon	NUP153	GRCh38.p7	6:17629370	TTCACTCATGGGGTT[A/T]ATAGACCCAGAATCG	9972
rs763775910	snp	A/T	0.00123796	0.0248485	intron-variant	NUP153	GRCh38.p7	6:17669079	GGAGTTATGAAAAAT[A/T]CCTTTTTTTTTTTTT	9972
rs763782177	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17640992	AGAATGTTTACATCT[-/AA]AGAGTAATGGTAGCT	9972
rs763785323	snp	C/G	1.6522e-05	0.00287414	missense	NUP153	GRCh38.p7	6:17616684	TGCTGCTGCCAAACT[C/G]GAAAGCCGAACCTGC	9972
rs763791822	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	NUP153	GRCh38.p7	6:17637430	TTGCACTAAACAGGT[A/G]TCACAATCCCAAGTG	9972
rs763792933	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17639702	ACCTACCTCTATTAA[C/T]GGAGAATCCATTTCC	9972
rs763845411	snp	A/T	1.64741e-05	0.00286998	missense	NUP153	GRCh38.p7	6:17637522	CACTTTTATTTGGTG[A/T]TTCAATTCCAGTCTG	9972
rs763852727	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	NUP153	GRCh38.p7	6:17688430	TGGCTCAGGTGTGAT[C/T]CTCCCATCAGTAATA	9972
rs763919327	snp	A/G	3.29669e-05	0.00405984	missense, intron-variant	NUP153	GRCh38.p7	6:17640017	CCTCACAATCTTCAG[A/G]TGGTGTCTTCTTACA	9972
rs763927274	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17648124	AGGTGGATATTTGTA[A/T]AAAAAAGTAAAGTAA	9972
rs763974516	snp	A/G	8.24409e-05	0.00641979	synonymous-codon, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632792	TCCTAGAGAGCCTCC[A/G]GAAGGCAGAGAGACA	9972
rs763981309	snp	C/T	1.75656e-05	0.00296353	intron-variant	NUP153	GRCh38.p7	6:17688346	TAGTGTCTTCAAAAT[C/T]AGGGCATGAAAACCT	9972
rs764016575	snp	A/G	1.6549e-05	0.0028765	intron-variant	NUP153	GRCh38.p7	6:17669380	TAAGATTTTTCAATA[A/G]TATCAAGTTTTGTTA	9972
rs764023695	in-del	-/CTGATC	1.91241e-05	0.0030922	intron-variant	NUP153	GRCh38.p7	6:17629579	TAGACACTCAATGTA[-/CTGATC]CTGATCCTCTCAAAC	9972
rs764042430	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636242	TGAGAGGCTGAGGCA[C/T]AAGAATTGCATGCAT	9972
rs764053069	snp	A/G	5.24462e-05	0.00512058	missense	NUP153	GRCh38.p7	6:17628703	AAGTGGCTTTTGCTG[A/G]CTGTTCAGATTCCTT	9972
rs764071530	snp	C/G	1.64863e-05	0.00287104	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632679	TTTGTGCCTGGCTTT[C/G]CACTTTCACATGCCA	9972
rs764101084	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17693354	AGATATTAAACACTA[C/G]ATATTAGAGAATGGG	9972
rs764105863	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17644157	AAGCCAAAGATATTT[C/G]TTTAGCTTCTATGTC	9972
rs764164094	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17646559	ACTTTCACCTATTTT[A/C]AGATATAGTTTATAA	9972
rs764168929	snp	C/G	2.78486e-05	0.00373142	intron-variant	NUP153	GRCh38.p7	6:17624853	AGGCCCAAAGAAACA[C/G]TTAAGTCACCATGGT	9972
rs764176194	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17645261	AAAAAAAAAAAAAAA[-/G]AATTCTATGTTTTAA	9972
rs764191937	snp	G/T	1.64803e-05	0.00287052	missense	NUP153	GRCh38.p7	6:17629101	GTGTTAGCAGGAGCA[G/T]GGGTGGAGTTAATAA	9972
rs764247027	snp	A/G	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17624723	ATCCAAAGCCTGGGG[A/G]ATTGGGCTGGCTGGC	9972
rs764258393	in-del	-/TCTCTC			intron-variant	NUP153	GRCh38.p7	6:17618557	TAGTGGAAGTTAAAA[-/TCTCTC]TTTTTTTTTTTTTTT	9972
rs764280472	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17654900	ACAGCTATTAAGTGG[C/T]AGAAATCTTACAGAC	9972
rs764299096	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17617031	CTGGATTACAGGCGT[A/G]AGCCACTGCACCCGG	9972
rs764303696	snp	A/C	1.85012e-05	0.00304143	intron-variant	NUP153	GRCh38.p7	6:17637806	AGTGCAACGTTAGAG[A/C]AGCTTTATAAATCAA	9972
rs764328569	snp	A/G	4.99023e-05	0.00499486	intron-variant	NUP153	GRCh38.p7	6:17661607	ACCACCACCACACCA[A/G]TGCTTTTTAAATAAA	9972
rs764335277	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17655664	TCACCATGTTGGCCA[C/G]GCTGGTCTCGAGCTC	9972
rs764335513	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643288	GACCAGCCTGGCAAC[A/G]TGACGAAACCCCTTC	9972
rs764336007	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17672323	TGGTTCATGCTTGTA[A/T]TCCGAACACTTTGGG	9972
rs764344269	snp	C/T	1.65002e-05	0.00287225	synonymous-codon	NUP153	GRCh38.p7	6:17674923	ATAAGGTGTATTTCG[C/T]AGTTTAGACTGTCTT	9972
rs764353240	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644958	AGGCGTGGTGGCAGG[C/T]GCCTGTGGTGCCAGC	9972
rs764391616	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17683421	ACATTGTATTATCAA[A/G]CATCAGAACAACATT	9972
rs764422038	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17654220	CTGTCCAACCTCCAG[C/T]GTAGAACCCTAAAAA	9972
rs764432114	snp	C/T	1.68479e-05	0.00290236	intron-variant	NUP153	GRCh38.p7	6:17661826	ATATATTATTGTGGT[C/T]CATAACTTGTTAACT	9972
rs764455717	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17621535	TAAAAGAAAATAACA[G/T]CTTGTCATTTACTAC	9972
rs764485714	snp	C/T	1.69758e-05	0.00291335	intron-variant	NUP153	GRCh38.p7	6:17688651	ATATTATGACAGTTT[C/T]AGAAATTTATCTTTT	9972
rs764487354	snp	A/G	4.94523e-05	0.00497229	intron-variant	NUP153	GRCh38.p7	6:17662005	AGTATAGCTGTATAA[A/G]AAATGACAGTACCTT	9972
rs764504937	snp	C/T	4.94181e-05	0.00497057	missense	NUP153	GRCh38.p7	6:17637291	TGGTTACAGTGCAGC[C/T]GGAAGATGAAGCAGT	9972
rs764588482	snp	G/T	1.72403e-05	0.00293596	intron-variant	NUP153	GRCh38.p7	6:17616521	TTCAATAAAAAATTC[G/T]CTTACCCCACTGTAA	9972
rs764590727	snp	C/T	1.65081e-05	0.00287293	synonymous-codon	NUP153	GRCh38.p7	6:17637190	CACACACTTATTGTC[C/T]TCTGCATTATTAGAA	9972
rs764592888	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690494	TATTATTTATAGTAA[C/T]TATAATGAAAATCAA	9972
rs764609857	snp	C/T	0.000117095	0.00765074	intron-variant	NUP153	GRCh38.p7	6:17669587	GTTGCAACATAAAAT[C/T]TAAGGCACATATTTC	9972
rs764610591	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17634588	ATTACGGGCATCCAC[C/G]ACCACGCCCAGCTAA	9972
rs764611459	in-del	-/GGGGCGGGTAAG			cds-indel, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706415	GCCGCTTCCCGCTCC[-/GGGGCGGGTAAG]GGGGCGGGAGAGGCA	9972
rs764632706	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17698895	AAAAGAAAACTCAAT[-/A]AAAGCTCACAGTAGT	9972
rs764657601	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644407	CTAATGCAGTCAGAA[C/T]AAAATCCAATTCATT	9972
rs764663223	snp	A/G/T	6.62717e-05	0.00575605	missense	NUP153	GRCh38.p7	6:17626111	TGGCTGGTGTACTTG[A/G/T]ACTAGAGGAACTGTT	9972
rs764667641	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701094	GCTGGGAGTGGTGGC[A/G]CATGCCTGTAATTCC	9972
rs764674455	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17639524	TCAATTCAAGTGAGT[A/C]CTGCTCCCTATGTAT	9972
rs764723538	snp	C/T	3.34947e-05	0.00409221	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706287	CATACCTGATGCTGT[C/T]GTCGCCCCTGCTGGT	9972
rs764725325	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627779	GAAGATGATGCTAAT[C/T]TGATACCTGCCTATT	9972
rs764727532	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17640687	AGTGGTGCAATCATA[A/G]CTTAATGCATCCTCA	9972
rs764741798	snp	A/G	1.69189e-05	0.00290846	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706349	CGTCCGGATCTTGCC[A/G]CCACCGCCCCCTCCG	9972
rs764753488	in-del	-/AAG			intron-variant	NUP153	GRCh38.p7	6:17630671	ACTTCAAAATAAATA[-/AAG]AAAAGAAAACAGAGG	9972
rs764759815	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690367	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	9972
rs764806617	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678843	CCAGCTACTCAAGGA[A/G]GCTGAGGTGGGAGGA	9972
rs764842214	snp	C/G	0.000108713	0.0073719	missense	NUP153	GRCh38.p7	6:17628673	CTGTAGTACTAGTTT[C/G]AGCTCCAAAGGCAAA	9972
rs764856479	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17649536	AATTGGTAAAACTGA[C/G]GGAAAAAAGATAGTA	9972
rs764866163	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679922	GAAATAACTGATTTA[C/T]AGCATTGTTGCCACC	9972
rs764881956	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641688	GAAACCCCGTTTCTA[C/T]TAAAAATACAAAACA	9972
rs764895298	snp	A/G	1.64779e-05	0.00287031	missense	NUP153	GRCh38.p7	6:17628786	TCTTTGGTTTGCTCT[A/G]AATTCCCAAAGGAAA	9972
rs764904144	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17666700	AACTCAATTTATTAT[C/G]TAAGTACACCAACTG	9972
rs764914520	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17619871	GGGAGGCCGAGGCGG[C/G]CAGATCACCTGAGGT	9972
rs764914694	snp	C/G	0.000148447	0.00861404	missense	NUP153	GRCh38.p7	6:17675725	TGAAGAGAAGGCCTT[C/G]TTAACACATCTGGAT	9972
rs764918281	snp	A/G	5.48712e-05	0.00523761	intron-variant	NUP153	GRCh38.p7	6:17669063	CTATTAGAATAGATG[A/G]GGAGTTATGAAAAAT	9972
rs764940879	snp	G/T	1.64751e-05	0.00287007	missense	NUP153	GRCh38.p7	6:17647862	ATTGGAGATGAAAAT[G/T]TAAACATGGGACTGC	9972
rs764968793	snp	C/T	1.648e-05	0.0028705	missense	NUP153	GRCh38.p7	6:17616170	GAAGAGAACACATTT[C/T]TCCCATTTGACCTGT	9972
rs764980360	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677144	CCTAAAAAGCCACAG[A/G]GGAGACAGAGCTTGG	9972
rs764980378	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654661	TTTCTACTCCCCCAA[A/G]TTTTGACTTAGTAGA	9972
rs764994002	snp	A/G	1.68216e-05	0.00290009	intron-variant	NUP153	GRCh38.p7	6:17649142	ACAAATGTCACCTGT[A/G]TTTATATAATGGTTT	9972
rs765054201	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688339	AACTAGGTAGTGTCT[C/T]CAAAATTAGGGCATG	9972
rs765070329	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17685324	AGGCTGAGGAAGGTG[C/G]ATCATGAGGTCAGGA	9972
rs765072411	snp	C/T	1.65034e-05	0.00287253	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632668	TAAACCCAGATTTTG[C/T]GCCTGGCTTTGCACT	9972
rs765078752	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633990	ACTGTAGTCTCTTAG[C/T]TGGTGACTCCACTGT	9972
rs765088958	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17696498	CGGTGGCTCACGCCT[C/G]TAATCCCAGTACTTT	9972
rs765089329	snp	A/C/G	0.000127791	0.00799253	intron-variant	NUP153	GRCh38.p7	6:17637803	GAGAGTGCAACGTTA[A/C/G]AGAAGCTTTATAAAT	9972
rs765138655	snp	C/T	8.32286e-05	0.00645038	intron-variant	NUP153	GRCh38.p7	6:17675813	ATATACAACTTAGAG[C/T]GATACACTACCACAA	9972
rs765160446	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17684608	TTTTAATTTCCATCA[A/G]TAACTTTTCCTTTGC	9972
rs765167496	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617265	TGAAATCAACAAATA[C/T]ACTTAGCTCTATCTT	9972
rs765169205	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17695840	CGGTGAAACCCTGTC[G/T]CTACTAAAAATACAA	9972
rs765173261	snp	A/G	5.10044e-05	0.00504971	missense	NUP153	GRCh38.p7	6:17637761	GAATCTATCTTCGGC[A/G]ATGCGAAACCTACAA	9972
rs765182622	in-del	-/AAGTCTGAG	1.64976e-05	0.00287202	cds-indel	NUP153	GRCh38.p7	6:17629447	TTCCAGTGCTTGTTA[-/AAGTCTGAG]AAGGCCCAGAAGAGG	9972
rs765186013	snp	A/G	1.73441e-05	0.00294478	intron-variant	NUP153	GRCh38.p7	6:17668940	ACAACAAAATTGTAG[A/G]CAGTTTAAATAACTA	9972
rs765217877	snp	A/C			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615101	AATTATACTGTAATA[A/C]ACATGGCTTTAATAT	9972
rs765239568	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667606	GTAGTCCCAGCTACC[C/T]GCGAGGCTGAGGCAG	9972
rs765296434	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17656838	CATGCCTCTTTATGG[A/G]CCACATGTGCAAATT	9972
rs765354083	snp	C/T	1.64743e-05	0.00287	synonymous-codon	NUP153	GRCh38.p7	6:17624616	AGGTTGCTGTCCAAA[C/T]ACAGGGGGCTGGCTA	9972
rs765375234	snp	G/T	0.000141955	0.00842361	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17651903	GCTCGAGATCAGCTT[G/T]GGCAATACGGTGAGA	9972
rs765386461	snp	C/T	1.66582e-05	0.00288597	intron-variant	NUP153	GRCh38.p7	6:17669573	ACCCTATATTATTTG[C/T]TGCAACATAAAATCT	9972
rs765411281	snp	A/C	3.29516e-05	0.00405891	missense	NUP153	GRCh38.p7	6:17629021	ATGTGAAAGGAGCCA[A/C]TGAAGCACTCTTGGT	9972
rs765445878	snp	C/T	3.29451e-05	0.00405851	missense	NUP153	GRCh38.p7	6:17637397	ACAGGCTACACATTT[C/T]ATTGCTTCAGGTTTA	9972
rs765474007	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676921	CCACCTAAGCCTTAC[A/G]CAGCAGCTGCTATGG	9972
rs765475240	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664851	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	9972
rs765510978	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17649903	CTTGGAACATATCCC[C/T]TGCAGATAAGGGGGT	9972
rs765519892	snp	C/T	1.65751e-05	0.00287876	intron-variant	NUP153	GRCh38.p7	6:17688622	GCTAAGAATGCCCTG[C/T]TGAGAGAAAAAACAT	9972
rs765528622	in-del	-/A	1.65168e-05	0.00287369	intron-variant	NUP153	GRCh38.p7	6:17669408	TTACACTCCTGTATT[-/A]ATCGTGATTTTAAAA	9972
rs765538950	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708585	AATCTCAGGTGATCT[A/G]CCCACGGCCTCCCAA	9972
rs765556798	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17637086	TCTAAAACAAGGATT[C/T]TTAGAATAAATTAAA	9972
rs765567823	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659994	CCTCCAGACCAGCAA[C/T]AGAGCCAAGTCTACT	9972
rs765570830	in-del	-/TTT			intron-variant	NUP153	GRCh38.p7	6:17618566	TTAAAATCTCTCTTT[-/TTT]TTTTTTTTTTTTTTA	9972
rs765593334	in-del	-/CTAT			intron-variant	NUP153	GRCh38.p7	6:17654778	ACATTTCACAATTCA[-/CTAT]CTAATACCTTTGTAA	9972
rs765629336	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673198	ATGGTGAGAAACTCC[A/G]TCTCTACTAAAAATA	9972
rs765636879	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17700120	AAGCAGGAAAATTCA[C/G]AGACAATATGAAGAC	9972
rs765654663	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642994	GAGACAGAACACAAG[C/T]TGACAGTTAGCTAGG	9972
rs765657384	snp	C/T	2.00946e-05	0.00316969	intron-variant	NUP153	GRCh38.p7	6:17646175	AAGAGAAAGAATATC[C/T]TTATACTTCGTTTTC	9972
rs765665687	snp	A/C	1.69697e-05	0.00291283	intron-variant	NUP153	GRCh38.p7	6:17665228	ACTGGTAGAAATATA[A/C]ATATACTCACACTGC	9972
rs765669291	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17659560	TCACTGCAACCTCCA[A/C]CTCCAGGGTTCAAGT	9972
rs765695574	in-del	-/ATATAC	3.42319e-05	0.004137	intron-variant	NUP153	GRCh38.p7	6:17665223	CAAAGACTGGTAGAA[-/ATATAC]ATATACTCACACTGC	9972
rs765715031	snp	A/C	1.64743e-05	0.00287	missense	NUP153	GRCh38.p7	6:17688538	TGAACAGCTGCATAC[A/C]TCTTCATTCTTGTTG	9972
rs765744871	snp	A/T	0.000392619	0.0140055	intron-variant	NUP153	GRCh38.p7	6:17628640	TAATAATAATAATAA[A/T]AAGTTAATACTTACC	9972
rs765745419	snp	C/T	1.91745e-05	0.00309627	missense	NUP153	GRCh38.p7	6:17646079	TACCTGAACTACTTA[C/T]AATTGGTTCTAAAGT	9972
rs765755308	snp	G/T	1.64795e-05	0.00287045	missense	NUP153	GRCh38.p7	6:17665322	AATAAACACTTCGAT[G/T]TGTTGCTATGGAAAC	9972
rs765779180	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17685064	GAAAAATGGCACTGA[A/T]CAACTTTCTTGACAT	9972
rs765799357	snp	A/G	3.29761e-05	0.00406041	missense	NUP153	GRCh38.p7	6:17626017	CTCACAGGATTGCTG[A/G]ACTGTCCAAACACAA	9972
rs765811228	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17683145	AATCAACTTTCTCTA[A/G]ACTCCTATTCATGTC	9972
rs765813073	snp	A/T	1.65004e-05	0.00287227	missense	NUP153	GRCh38.p7	6:17629423	CTCCCTGATCTCCAA[A/T]TTTAAAATTTCCAGT	9972
rs765858399	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672173	ACCTACCGGGAAGCC[C/T]ATGGCAATCAAGACA	9972
rs765882906	snp	C/T	1.72829e-05	0.00293959	intron-variant	NUP153	GRCh38.p7	6:17688662	GTTTTAGAAATTTAT[C/T]TTTTTAAAATAAGTA	9972
rs765889878	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17619973	TGTGGTGGCACGCGC[A/C]TGTAATCCCAGCTAC	9972
rs765928455	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17672047	CAAAATCCTAGCAGA[A/C]TGTAGAAACAAGCCA	9972
rs765945481	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659445	AATTCCTTATTTACA[C/T]AAGGTAAGACAGCCC	9972
rs765946861	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17617370	TTGATACTAAACGAG[C/G]AGTAGGGAAAGAACA	9972
rs765949091	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17621270	TGAATGTAAATTAGT[A/C]TAACCGTTATGGAAA	9972
rs765950725	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688306	ATGGTTTATGTACCG[C/T]CTGATTAGATTTACC	9972
rs765968341	snp	C/T	6.93794e-05	0.00588939	intron-variant	NUP153	GRCh38.p7	6:17668935	TAAACACAACAAAAT[C/T]GTAGACAGTTTAAAT	9972
rs765969624	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17690301	AGCTTGCAGTGAGCC[C/G]AATGTGCAGTAAAAT	9972
rs765981094	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17695759	TCACGCCTGTAATCC[A/C]AACACTTTAGGAGGC	9972
rs766046844	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677231	AATATACATTAATAC[A/G]GCACAAAACTACATC	9972
rs766048422	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17659872	CTGTTTGTATGATCA[A/G]TGGCATTCAAGGTAT	9972
rs766052234	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648386	CTTTGGGAGGCCAAG[A/G]CAGGCGGATCACCTG	9972
rs766054196	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641429	AGTCTCAGCTACTCA[A/G]GAGGCTGAGGCAGGA	9972
rs766058864	snp	C/T	3.29859e-05	0.00406102	missense	NUP153	GRCh38.p7	6:17665364	TCATAAGTCTCTGAA[C/T]AGGAGGATATTGAGA	9972
rs766079870	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708051	GTGGCGCGATCTTGG[C/T]TCACTGCACCCTTTG	9972
rs766086537	snp	C/G	1.65792e-05	0.00287912	synonymous-codon	NUP153	GRCh38.p7	6:17626118	TGTACTTGAACTAGA[C/G]GAACTGTTGTTCAAG	9972
rs766091852	snp	A/G	1.64866e-05	0.00287106	missense	NUP153	GRCh38.p7	6:17675708	AATTCAGATGGCTCC[A/G]ATGAAGAGAAGGCCT	9972
rs766103604	in-del	-/AGAAAATAGCAA	1.64817e-05	0.00287064	cds-indel	NUP153	GRCh38.p7	6:17625944	TAGTTTGCTATCTTG[-/AGAAAATAGCAA]AGACTGAGAGGTGCT	9972
rs766129229	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17627695	ATTTGGCTAGTAACA[A/G]AATTCTAGGTTCAAG	9972
rs766151383	snp	A/C	1.65149e-05	0.00287353	synonymous-codon	NUP153	GRCh38.p7	6:17629466	CTGAGAAGGCCCAGA[A/C]GAGGATGATGAGACA	9972
rs766210378	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17695833	GCTAACACGGTGAAA[A/C]CCTGTCTCTACTAAA	9972
rs766226481	snp	A/G	1.68644e-05	0.00290378	missense	NUP153	GRCh38.p7	6:17637752	GCAGCAACAGAATCT[A/G]TCTTCGGCGATGCGA	9972
rs766227352	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674613	GTCTCTACTAAAAAT[A/G]CAAAAAATTAGCTGG	9972
rs766241075	snp	A/G	0.000769527	0.0196003	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17651912	CAGCTTGGGCAATAC[A/G]GTGAGACCTTGTCTC	9972
rs766245638	snp	C/G/T	8.2383e-05	0.0064176	missense	NUP153	GRCh38.p7	6:17624599	CCAAATGCAGACTGA[C/G/T]TAGGTTGCTGTCCAA	9972
rs766291614	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17626865	AAATTATGGGAGGAG[A/G]AAGGGAATACCTTCA	9972
rs766312654	snp	C/G	1.64819e-05	0.00287066	missense	NUP153	GRCh38.p7	6:17637674	CCAAACCCAATTCCA[C/G]TAGAAGAAAAGCTAC	9972
rs766328962	snp	C/G	1.6486e-05	0.00287102	missense	NUP153	GRCh38.p7	6:17661656	ATACAACCCTACCTC[C/G]TCCTCCAGAGGTTTA	9972
rs766330968	in-del	-/T	1.80523e-05	0.0030043	intron-variant	NUP153	GRCh38.p7	6:17616505	AATGTAACTTCTCCA[-/T]TTCAATAAAAAATTC	9972
rs766336273	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17638719	TAAGAAGTAAAAAGG[A/G]AGCAGGGGGAGGTTG	9972
rs766384830	snp	C/G	1.64762e-05	0.00287016	missense	NUP153	GRCh38.p7	6:17629010	TGATGTCTTACATGT[C/G]AAAGGAGCCACTGAA	9972
rs766453043	snp	G/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17688518	GGAACCTCGCTTGTG[G/T]CTGTTGAACAGCTGC	9972
rs766470226	snp	C/T	1.64754e-05	0.00287009	missense	NUP153	GRCh38.p7	6:17688441	TGATTCTCCCATCAG[C/T]AATATTAGAGCTCTC	9972
rs766488954	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17624136	CAAATGGAAAGGCTG[A/G]TATCATCAGTAAATA	9972
rs766516889	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690865	GAAAAGGTAGCCGGG[C/T]GTGGTGGCTCACGCC	9972
rs766526761	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17635842	CTGAAAATGATGGTT[A/C]ATCATTGAAAGGAGG	9972
rs766560535	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17686355	ACTTTATGTAGGGCT[A/G]GGTTAATGTGCGCAT	9972
rs766577569	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635837	CTCTGCTGAAAATGA[C/T]GGTTCATCATTGAAA	9972
rs766593548	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17703138	AGGAGGCAAAGGTTG[C/T]AGTGAGCCAAGATCG	9972
rs766602428	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17694381	TAAAGGATAGGAGCT[-/G]GGCCCGGTGGCTCAC	9972
rs766607341	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17675840	ACAAATGGTTTTTAC[C/T]TTAAGAAAACACATT	9972
rs766614809	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17704051	TAATCCCAGCACTTC[C/G]GGAGGCCGAAGCGGG	9972
rs766620970	snp	C/G	1.64757e-05	0.00287012	synonymous-codon	NUP153	GRCh38.p7	6:17628923	CACTGAGGCAGATGG[C/G]AGAGAGGCAGGCTCC	9972
rs766623299	snp	A/G	1.66721e-05	0.00288717	missense	NUP153	GRCh38.p7	6:17637167	CCTGGTTTCTCAGAC[A/G]TACAGGACACACACT	9972
rs766624848	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667591	TGGTGATAGGCGCCT[A/G]TAGTCCCAGCTACCT	9972
rs766636477	in-del	-/ATT	1.64991e-05	0.00287215	cds-indel	NUP153	GRCh38.p7	6:17637196	CTTATTGTCTTCTGC[-/ATT]ATTAGAAACACAGCA	9972
rs766711664	snp	C/T	1.66192e-05	0.00288259	missense	NUP153	GRCh38.p7	6:17675366	TCTTTGAAACAGTTA[C/T]ATCTGAAACAAAATT	9972
rs766713023	snp	A/G	0.000221198	0.0105143	intron-variant	NUP153	GRCh38.p7	6:17632865	AAAAAAAAAAAAAAC[A/G]GGGAGTGGGGGGAGA	9972
rs766747214	snp	C/T	1.64795e-05	0.00287045	missense	NUP153	GRCh38.p7	6:17662063	GTCATATTTTTTTCA[C/T]ATCCAGTCTGCAGGG	9972
rs766773126	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17622961	CGGTGAAACCCCATC[G/T]CTACTAAAAATATAA	9972
rs766781428	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17653396	CACAAACCAGAATGA[C/T]TAAAATTTAAAAGAT	9972
rs766799140	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642922	AAGAACTCAGCTGTA[C/T]GAAGCCACATTGTAT	9972
rs766804576	snp	A/C/T	3.3093e-05	0.00406763	missense, intron-variant	NUP153	GRCh38.p7	6:17640056	TGTTCACTGTAGTGA[A/C/T]ATGATGAGCTGTAAT	9972
rs766804663	in-del	-/A	1.66729e-05	0.00288724	intron-variant	NUP153	GRCh38.p7	6:17661801	AATAAAAAGAAAATT[-/A]AAACAACTGATATAT	9972
rs766836011	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17619146	AGGCCAAAGAGCAAA[-/G]GATCAAGACTTCAGG	9972
rs766836100	snp	A/G	1.64846e-05	0.0028709	synonymous-codon	NUP153	GRCh38.p7	6:17675250	AAGTGTTCCAAAGGC[A/G]GACAAGTTGAATGCT	9972
rs766900029	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630347	CAGAAGAATTACAGA[A/G]TTGAAGCAATGTTTA	9972
rs766915285	snp	G/T	1.64808e-05	0.00287057	missense	NUP153	GRCh38.p7	6:17675605	GAATCTTTAATTTCC[G/T]TTACAAGGGAAAATC	9972
rs766951098	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693502	TCCTAGAGAAGGTAG[C/T]AGCGTTCTGCTATTG	9972
rs766974357	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705023	CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT	9972
rs767001352	snp	A/G	0.000131859	0.00811862	missense	NUP153	GRCh38.p7	6:17665351	ACTGGCTTTGGGGTC[A/G]TAAGTCTCTGAACAG	9972
rs767028057	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630122	AGTAAGAATATATAG[A/G]GGTATGTATGTTTGC	9972
rs767029559	snp	A/C	6.65779e-05	0.00576927	missense	NUP153	GRCh38.p7	6:17665243	CATATACTCACACTG[A/C]ACTTGTTATCTATTC	9972
rs767044345	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17682138	GTAAAGTGAGTCACA[C/T]ACGTTTTTGGTTTCC	9972
rs767057118	in-del	-/A	0.00118875	0.0243508	intron-variant	NUP153	GRCh38.p7	6:17674858	ATCCAGTTAAAGTGT[-/A]AAAAAAAAGAAAAAA	9972
rs767059647	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681140	ATAGATGGAACTGCA[A/G]AACATCACATTAAGT	9972
rs767062673	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17636488	ACTGCATATTCATGA[A/C]TAATGCATTGAAAAC	9972
rs767084080	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17681022	GAATTGACCTAAGTA[A/T]CCATCCACAAATGAA	9972
rs767128427	snp	A/G/T	9.92349e-05	0.00704334	missense	NUP153	GRCh38.p7	6:17669543	TTTGTCTTCTAACTG[A/G/T]TGCCTGTAAAGTAAA	9972
rs767156247	snp	A/T	1.66729e-05	0.00288724	intron-variant	NUP153	GRCh38.p7	6:17675471	CAGAAAAAAAACCCA[A/T]AAAATTTAATGTTAC	9972
rs767169050	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638568	GTGTTATTTTGCTTA[C/T]GATTAATTTAAATCA	9972
rs767184106	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698546	GATTGAGACCATCCC[A/G]GCTAACATGGTGAAA	9972
rs767192653	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17663940	CATGTCCACACACAC[-/AA]ACACACAAAAAAACA	9972
rs767201261	snp	C/T			missense	NUP153	GRCh38.p7	6:17629288	TATCTTTTTTAACTT[C/T]TTCGGGCTTAGATTC	9972
rs767219375	in-del	-/A	0.000345393	0.0131369	intron-variant	NUP153	GRCh38.p7	6:17624878	ATGGTGGCTAATGTC[-/A]AGATTATCCTCAAGA	9972
rs767233727	snp	A/G			missense	NUP153	GRCh38.p7	6:17629446	TTTCCAGTGCTTGTT[A/G]AAGTCTGAGAAGGCC	9972
rs767274453	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641649	ACGAGGTCAGGAGAT[C/T]GAGACCACCCAGGCT	9972
rs767285491	in-del	-/ACA	1.64901e-05	0.00287137	cds-indel	NUP153	GRCh38.p7	6:17616079	TTGTTAAAATTGAGT[-/ACA]ACACCAATGTGACCT	9972
rs767297033	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693701	GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCAG	9972
rs767300157	snp	C/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704960	AGGGACGGGGTTTCA[C/G]CGTCTCTGGATGGTC	9972
rs767337048	snp	A/G	0.000190132	0.00974833	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17651882	GATGATCGCTTGAGC[A/G]CAGGAGCTCGAGATC	9972
rs767353244	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706077	CGGCCCAAACCACAC[A/G]TGTGCGCCGCAAGGC	9972
rs767371417	snp	C/G	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17649264	AAGAACTGGTGATCG[C/G]TAGAGAGATTTTCGG	9972
rs767373621	snp	C/T	1.65214e-05	0.0028741	intron-variant	NUP153	GRCh38.p7	6:17669401	AGTTTTGTTACACTC[C/T]TGTATTAATCGTGAT	9972
rs767395742	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17648981	GAGGAACACTCCATT[A/T]TAATGTATCCAAGAT	9972
rs767413416	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17626715	TATAACTTTATACCA[C/T]GGACTGATATTAGTA	9972
rs767431452	snp	A/G	5.20156e-05	0.00509952	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706427	TCCGGGGCGGGTAAG[A/G]GGGCGGGAGAGGCAG	9972
rs767460551	snp	C/G	4.94279e-05	0.00497107	missense	NUP153	GRCh38.p7	6:17628815	AAACACTGGTTGACA[C/G]TTTGGCTCTTCATTG	9972
rs767479290	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648256	TTTGGGAAGCCATGA[C/T]AGAGGGAATTGCTTG	9972
rs767521568	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17688132	CAAAAAACAAAAAAA[A/C]GAAAGAAAAAAAGAA	9972
rs767521864	snp	A/G	1.64933e-05	0.00287165	missense	NUP153	GRCh38.p7	6:17616578	AAGCCCCCCGAGCCT[A/G]AAGGCTGGGCTGAGG	9972
rs767536071	snp	A/C	3.68433e-05	0.00429189	intron-variant	NUP153	GRCh38.p7	6:17632861	TAAAAAAAAAAAAAA[A/C]AACGGGGAGTGGGGG	9972
rs767553622	snp	A/C	1.76176e-05	0.00296791	intron-variant	NUP153	GRCh38.p7	6:17688351	TCTTCAAAATTAGGG[A/C]ATGAAAACCTATCAT	9972
rs767573619	snp	A/T	1.64798e-05	0.00287047	missense	NUP153	GRCh38.p7	6:17662051	TTTTGTCCGGGTGTC[A/T]TATTTTTTTCATATC	9972
rs767578345	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17622772	TTATAGTATACCATA[C/T]GGCTCAGCAATAATC	9972
rs767580446	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635814	ATACAAACTTGACTG[C/T]ATCACTCCTCTGCTG	9972
rs767644376	in-del	-/T	1.66157e-05	0.00288229	intron-variant	NUP153	GRCh38.p7	6:17649154	GTATTTATATAATGG[-/T]TTTTGTACCTTGTTT	9972
rs767686339	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684525	CTAAACCAACTCAAA[C/T]TTTCTACACATCAGC	9972
rs767694594	snp	C/T	4.15084e-05	0.00455549	intron-variant	NUP153	GRCh38.p7	6:17624875	CACCATGGTGGCTAA[C/T]GTCAGATTATCCTCA	9972
rs767703980	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17661420	GGTCAAATAATTTCA[A/C]TTGCAATTCCCTTAT	9972
rs767745826	snp	A/G	1.65004e-05	0.00287227	missense	NUP153	GRCh38.p7	6:17625831	CTAGATGTGGTTGTG[A/G]CTCCAAAGCCGAAAC	9972
rs767769189	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656787	GGAAGGAAAGAGGAA[C/G]TCTGAAAAGTCCTTC	9972
rs767795881	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17673437	TATTCGCAAAACATA[C/T]AACAAAGTATTTGTA	9972
rs767801630	snp	A/G	3.3678e-05	0.0041034	intron-variant	NUP153	GRCh38.p7	6:17639906	TGAGATCATGAGTTT[A/G]TAATCAAAAGGCTTA	9972
rs767833723	snp	A/G	1.64923e-05	0.00287156	missense	NUP153	GRCh38.p7	6:17675239	CTCACAGGGGAAAGT[A/G]TTCCAAAGGCAGACA	9972
rs767859548	snp	C/T	1.64966e-05	0.00287194	missense, intron-variant	NUP153	GRCh38.p7	6:17640040	TTCTTACAATTTGTA[C/T]TGTTCACTGTAGTGA	9972
rs767860134	snp	C/T	3.29462e-05	0.00405857	missense	NUP153	GRCh38.p7	6:17637315	AAGCAGTCATAGTCT[C/T]AGCACTTTCCGAAAC	9972
rs767879812	in-del	-/G	0.000224117	0.0105834	intron-variant	NUP153	GRCh38.p7	6:17632872	AAAAAAACGGGGAGT[-/G]GGGGGAGATTTCATG	9972
rs767892886	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17662370	CCTCTTTTTGTCCTG[C/T]TAATTGTGCAACCAA	9972
rs767896842	snp	C/T	3.2963e-05	0.00405961	missense	NUP153	GRCh38.p7	6:17674958	CAGCTGCTGCCCCAC[C/T]GTATGTTGTTTTTCC	9972
rs767926250	snp	A/C	1.65425e-05	0.00287593	missense	NUP153	GRCh38.p7	6:17629195	GTCCAAGATTAGATA[A/C]CCCAAATTGAAATGG	9972
rs767937053	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653192	TGGGAGGTGGAGGCT[A/G]CAGTGAGCCAAGATC	9972
rs767937148	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17640910	TTACTGGCATGAGTC[A/T]TCATGCCTGGCCCAC	9972
rs767939333	in-del	-/AAT			intron-variant	NUP153	GRCh38.p7	6:17668855	CTCAAAAAAAAAAAG[-/AAT]ATTATTTTTCAAACA	9972
rs768003375	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17654049	CTTTTTTGATAAAGC[A/C]AATGTAACACAAAAT	9972
rs768014229	snp	A/C	1.64836e-05	0.0028708	missense	NUP153	GRCh38.p7	6:17629113	GCAGGGGTGGAGTTA[A/C]TAACACCTGTACCAA	9972
rs768058437	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642449	ATGGACAATAAGCAC[C/T]TGAAAAAAATGCAAC	9972
rs768068051	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17622783	CATATGGCTCAGCAA[C/T]AATCAGCATTTCCAT	9972
rs768072517	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692458	ATTCAAGGTTGCAGT[C/T]AGCTATGATTGTACC	9972
rs768102569	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17702830	TCTTAAGAGTTATTA[-/C]CCCTTATAACTCTTC	9972
rs768116094	snp	A/G	1.66283e-05	0.00288338	intron-variant	NUP153	GRCh38.p7	6:17624551	ACTAACAGCATCACA[A/G]CACACTTACTAGAAT	9972
rs768123981	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17650557	ATACTTCAAATGGAT[A/G]CAGTTTATTGCAAAT	9972
rs768193257	snp	A/G	1.73534e-05	0.00294558	intron-variant	NUP153	GRCh38.p7	6:17637140	AAATTACTCCATAAA[A/G]CCAAAAACATACCTG	9972
rs768222533	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681980	TAGGAGGCTGAGGCA[A/G]GAGGATCACTTAAGG	9972
rs768258636	snp	C/T	1.65405e-05	0.00287576	intron-variant	NUP153	GRCh38.p7	6:17661636	AACCTCAAGAGTATA[C/T]GAGTATACAACCCTA	9972
rs768285161	in-del	-/CTG			intron-variant	NUP153	GRCh38.p7	6:17644334	CTAGCACTCACCACA[-/CTG]CTATCACTATACTCA	9972
rs768286949	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17625300	TCAGCACTTTGAAAG[C/G]CCGAGGCGGGCAAAT	9972
rs768294403	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17628879	GTGACAGGCTCTTGC[C/T]GTTTCTCTTCTGTCC	9972
rs768320772	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17693126	TTTTTCTCTGAATCC[A/C]CTCACTTGGATTTAA	9972
rs768343774	in-del	-/GAT	1.64742e-05	0.00286999	cds-indel	NUP153	GRCh38.p7	6:17624697	AATAATGCTGTGGAA[-/GAT]GATGATATAGATCCA	9972
rs768349114	snp	A/G	1.64779e-05	0.00287031	missense	NUP153	GRCh38.p7	6:17628969	AATCCTCCTTTGGTG[A/G]CAGGCATTTCTTCTT	9972
rs768382937	snp	G/T	1.65064e-05	0.00287279	missense	NUP153	GRCh38.p7	6:17669531	GCTTAGCTTTCATTT[G/T]TCTTCTAACTGGTGC	9972
rs768399213	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17653051	TTAGCTCAGGAGTTT[C/G]AGACCAGCCTGGGCA	9972
rs768411173	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17663134	CTTGTTAATAAGAAC[A/G]CAGAGAAAAAGATAG	9972
rs768414992	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620866	CAAAAATAGACAAGA[A/G]GGACTATATTAAACT	9972
rs768442132	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659713	CTTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	9972
rs768442580	snp	A/C	3.63702e-05	0.00426425	intron-variant	NUP153	GRCh38.p7	6:17632858	TCCTAAAAAAAAAAA[A/C]AAAAACGGGGAGTGG	9972
rs768459428	in-del	-/TA	4.96274e-05	0.00498109	intron-variant	NUP153	GRCh38.p7	6:17647919	CCTGGTTTTCCAAAT[-/TA]TATTAAGAAATGATA	9972
rs768468204	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664200	TAAGTGGCTACTGAC[A/G]GGTATGGGTATGAGA	9972
rs768517130	snp	C/T	1.75742e-05	0.00296425	missense	NUP153	GRCh38.p7	6:17646115	TAGAACCAGAAAGTT[C/T]TGCTGTTTTTGCAAC	9972
rs768521608	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17631347	AAGTAGATAAAGCTT[A/G]CTATTATTTTTGTTT	9972
rs768564954	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17688044	GAATGGCATGAATTC[A/G]GGAGGCGGAGCTTGC	9972
rs768574921	snp	C/T	1.64985e-05	0.0028721	synonymous-codon	NUP153	GRCh38.p7	6:17629391	CCCAGAATCGGATGA[C/T]ACACCTATTTTGAAT	9972
rs768576315	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17701224	AGCGAAACTCTGTCT[-/A]AAAAAAAAAAAAAAA	9972
rs768593150	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659143	CATCTGCCATATTCA[C/T]CTGACCTCTCGCCAA	9972
rs768648839	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684321	CAGCACTTGTTGCTT[C/T]ACCTTGCCCTTTTAT	9972
rs768664800	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17656690	CAACAAGGAAGACAG[C/G]AGTCCAGCTCAAATC	9972
rs768671034	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671616	GAAAAAAATTTATAA[A/G]CCACCTAAATGGGAA	9972
rs768685715	snp	C/T	1.64806e-05	0.00287054	synonymous-codon	NUP153	GRCh38.p7	6:17625929	GCTGGATGTGGTTGC[C/T]AGTTTGCTATCTTGA	9972
rs768698825	snp	A/G	3.29734e-05	0.00406025	intron-variant	NUP153	GRCh38.p7	6:17662115	TTGCTTATTTGTTGT[A/G]ATTTTCTTAGTACCA	9972
rs768728340	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17668380	CCACCGCACCTGGCC[A/G]ATCACTCCTATTTTT	9972
rs768740789	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674507	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCTAACA	9972
rs768773915	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676866	AAATCCACAAGGGAG[C/T]GTCCAGTGAGCAGAG	9972
rs768787037	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17619241	AATCTACATCTATAT[G/T]CAATCAAAATCTTAC	9972
rs768792462	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17667070	CGATACTCAACCATT[A/C]GTAAAACTGTTATTG	9972
rs768836960	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17696175	AAGGGACCCTGCCTA[A/C]CAAACAGATCTGGAG	9972
rs768838380	snp	A/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637374	CAAGTTCCAGGTTTC[A/G]GTGTTTCACAGGCTA	9972
rs768853088	snp	A/C/T	3.35504e-05	0.00409564	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706329	GGCCCCTGGTGGCAA[A/C/T]GCCGCGTCCGGATCT	9972
rs768895389	snp	A/T	4.94189e-05	0.00497062	missense	NUP153	GRCh38.p7	6:17637474	TAAATTTGTCTCCAA[A/T]GCCTGTCCCTGATGC	9972
rs768947158	snp	C/T	1.65217e-05	0.00287412	synonymous-codon	NUP153	GRCh38.p7	6:17629175	TTCCTCTTTCTTTTC[C/T]TCCTGTCCAAGATTA	9972
rs768960195	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17702409	GCTACTCGGGAGGCT[A/G]AGGCAGAAGAATGGC	9972
rs768963943	snp	A/G	3.43365e-05	0.00414332	intron-variant	NUP153	GRCh38.p7	6:17649127	AAGAATTAAGAAAGA[A/G]CAAATGTCACCTGTA	9972
rs768985027	snp	G/T	1.70313e-05	0.00291811	intron-variant	NUP153	GRCh38.p7	6:17616232	GCTCTGAGCAAAATT[G/T]CCAAATGCTAACATT	9972
rs768995066	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17655551	CTCCCCCTCCCAGGT[G/T]CAAGCGATTCTTCTG	9972
rs769012991	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17697175	GGATTAAAGGAGTGA[A/T]TTTTAGAATGTGAAC	9972
rs769021745	snp	C/T	1.65198e-05	0.00287395	intron-variant	NUP153	GRCh38.p7	6:17675218	TTAAATCCAACCCAG[C/T]TAGTACTCACAGGGG	9972
rs769042126	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17667044	CACCCATTAATAAAC[-/TT]TTATGGATACGATAC	9972
rs769043356	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17663225	TATTATGCTAAAAAG[-/A]AAAAAATACACACAC	9972
rs769062061	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632735	CTGCACTAGGCACAA[C/T]TCACAGTCCCAGCTT	9972
rs769074780	snp	A/C	1.64811e-05	0.00287059	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616094	ACAACACCAATGTGA[A/C]CTTTATTTCCTGCGT	9972
rs769077170	snp	A/T			missense	NUP153	GRCh38.p7	6:17675290	GAGCTGGTGGCAGTG[A/T]GCTGTGAGAGTGAGT	9972
rs769134675	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17691778	CTTAAAAACAAAGAC[A/G]TACTTGATATAGGTG	9972
rs769147365	snp	A/C	1.7357e-05	0.00294588	intron-variant	NUP153	GRCh38.p7	6:17668926	TGTGAACTTTAAACA[A/C]AACAAAATTGTAGAC	9972
rs769148952	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17644869	GGCAGGCAGATCACG[A/T]GGTTAGGAGATCGAG	9972
rs769172083	snp	A/G	1.7149e-05	0.00292817	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632628	TTTACCATCACCTTT[A/G]TTTTTATTTTTTTGG	9972
rs769182734	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17643528	TATGCCAAAACAAAC[-/TT]ATAATTTAATCACGT	9972
rs769188961	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653026	GGTAGGCCGAGGCGG[A/G]TGGACTGCCTTAGCT	9972
rs769202315	snp	A/C/T	5.35789e-05	0.00517562	missense	NUP153	GRCh38.p7	6:17646099	GGTTCTAAAGTACTA[A/C/T]TAGAACCAGAAAGTT	9972
rs769212790	in-del	-/AAAC			intron-variant	NUP153	GRCh38.p7	6:17641549	AAAACAAAACAAAAC[-/AAAC]AAACAAACAAACAAA	9972
rs769224325	snp	C/T	3.32204e-05	0.00407542	intron-variant	NUP153	GRCh38.p7	6:17675795	AAAGCATTAATATTA[C/T]GAATATACAACTTAG	9972
rs769230774	snp	A/G	6.59e-05	0.00573983	missense	NUP153	GRCh38.p7	6:17628871	AAGTAGAAGTGACAG[A/G]CTCTTGCTGTTTCTC	9972
rs769264712	snp	A/G	1.64795e-05	0.00287045	missense	NUP153	GRCh38.p7	6:17688417	TATTACTGACTGCTG[A/G]CTCAGGTGTGATTCT	9972
rs769301556	snp	A/T	5.07335e-05	0.00503629	intron-variant	NUP153	GRCh38.p7	6:17640078	AGCTGTAATTTTTTT[A/T]AATTTAATAACATTA	9972
rs769309832	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17674233	AATGTCTGATCAATA[G/T]TTGATTGTAGAAGTG	9972
rs769371340	in-del	-/TAC			intron-variant	NUP153	GRCh38.p7	6:17637842	TAATTTGATTATTAT[-/TAC]TGAGAAGACGTTTAC	9972
rs769379140	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17696775	ATAAAACAAATAAAT[-/A]AAAATCTTAAAAAAC	9972
rs769386920	snp	C/T	6.59348e-05	0.00574135	missense	NUP153	GRCh38.p7	6:17669445	CGCTAAAGGGCTTGA[C/T]ATCTTCTCTAAAGAC	9972
rs769401948	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674701	CTTGAAACCAGGAGA[C/T]GGAGGTTGCAGTGTG	9972
rs769406672	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632771	GGGTTTCTTGAACTT[C/T]TCCAATCCTAGAGAG	9972
rs769454160	in-del	AAAA/GATAATTACAATCTTTGC			intron-variant	NUP153	GRCh38.p7	6:17699508	AAAAAGAAAATACAA[AAAA/GATAATTACAATCTTTGC]AATACTCTGTGCCTA	9972
rs769457072	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17623446	CTCATACAATGGTGG[G/T]AGGATATGAATTGGC	9972
rs769459815	snp	A/G	0.000436459	0.0147661	intron-variant	NUP153	GRCh38.p7	6:17632848	GTACTGAACTTCCTA[A/G]AAAAAAAAAAAAAAA	9972
rs769524305	snp	C/T	1.64846e-05	0.0028709	intron-variant	NUP153	GRCh38.p7	6:17662107	ATTTACGTTTGCTTA[C/T]TTGTTGTAATTTTCT	9972
rs769531705	in-del	-/TTTTTTTTTTTTTT			intron-variant	NUP153	GRCh38.p7	6:17635105	ACAGCTTGGCTTATC[-/TTTTTTTTTTTTTT]TTTTTTTTTGAGACG	9972
rs769541643	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17642332	TCACGTATCTGGTAA[C/G]GGTCTAGTGTCCAGA	9972
rs769556009	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674103	TGACTAAACGTATAT[A/G]ACATTCTGGAAAGGC	9972
rs769594088	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680545	TGACAATGATTTATC[A/G]GATACAACACTAAAA	9972
rs769637209	in-del	-/GAG	0.000181212	0.00951698	cds-indel	NUP153	GRCh38.p7	6:17616158	GAAGTTCCAGAAGAA[-/GAG]AACACATTTTTCCCA	9972
rs769680514	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17624222	GGGGTAACTTCCTAA[C/T]GCAAATCCAATCATA	9972
rs769689036	snp	A/G	1.64819e-05	0.00287066	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639994	GATTTCTGCAGGTCT[A/G]AAAGGACCCTCACAA	9972
rs769689375	in-del	-/T	6.77254e-05	0.00581877	intron-variant	NUP153	GRCh38.p7	6:17646196	TTCGTTTTCAATAAG[-/T]TATCAAATATAGAGC	9972
rs769691298	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697507	CCTGGCCAACATGGC[A/G]AAACCCTGTCTCCAT	9972
rs769776898	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17641316	CCAAGGCGGGCAGAT[C/T]ACGAGGTCAAGAGAT	9972
rs769787776	in-del	-/CTCCTGGGCTCAAG			intron-variant	NUP153	GRCh38.p7	6:17665912	CAGGCTGGTCTCAAA[-/CTCCTGGGCTCAAG]CAATCTGCCTGCCTC	9972
rs769795854	snp	A/C	1.65499e-05	0.00287657	intron-variant	NUP153	GRCh38.p7	6:17675039	TCCCAAGTGACTGCA[A/C]AGAAACAGAATGATA	9972
rs769800640	snp	A/G	1.6483e-05	0.00287076	intron-variant	NUP153	GRCh38.p7	6:17662011	GCTGTATAAGAAATG[A/G]CAGTACCTTTCTCGT	9972
rs769805758	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666283	GCAATGTGGGAGGCC[A/G]AAGCAGGTGGATCAT	9972
rs769940574	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678127	TTGGGAGGCCAAGGC[A/G]GGCAGATGACTTGAG	9972
rs769957311	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17639052	ATTATCTCACAGTTT[G/T]ACATTCTTTTATTCT	9972
rs769983051	snp	C/G	1.64762e-05	0.00287016	missense	NUP153	GRCh38.p7	6:17647821	CAGATGATGGAGGTA[C/G]TACATTTGCCTCAGT	9972
rs769989179	snp	C/G	1.76871e-05	0.00297375	missense, intron-variant	NUP153	GRCh38.p7	6:17669015	GTGATATCTATCCCA[C/G]TCCTATCAAGAGGCT	9972
rs770009924	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644707	CAATACTTTGGGAGG[C/T]CAAGGTGGGCAGATC	9972
rs770036252	snp	C/T	1.672e-05	0.00289132	intron-variant	NUP153	GRCh38.p7	6:17647949	ACAAAAAGAGCTTTT[C/T]AGAAAAATAAAGTGA	9972
rs770045460	snp	A/G	1.84855e-05	0.00304013	intron-variant	NUP153	GRCh38.p7	6:17626214	CTTAAGAATAGTCTC[A/G]GAAAGTACTTTTTCC	9972
rs770046578	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634489	TTGCCCAGGGTGGAG[C/T]AGAGTGGCACAATCT	9972
rs770062920	snp	C/T	1.67284e-05	0.00289205	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706317	TAAGGCTTAATTGGC[C/T]CCTGGTGGCAACGCC	9972
rs770076031	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17617782	CCTAGGAGGTCGAGG[A/G]CGCAGTGTGCCCTGA	9972
rs770086707	snp	C/T	6.58913e-05	0.00573945	missense	NUP153	GRCh38.p7	6:17637285	TACCAGTGGTTACAG[C/T]GCAGCTGGAAGATGA	9972
rs770095066	snp	C/T	1.64838e-05	0.00287083	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616086	AATTGAGTACAACAC[C/T]AATGTGACCTTTATT	9972
rs770109505	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17668071	TTAGTTTACTGAACT[-/TT]TTTTTTTTTTTTTTT	9972
rs770156730	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696398	GAGTTCTTCAGGTCT[C/T]TACAGGAAATAAGCA	9972
rs770177422	in-del	-/C			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705942	AGAACATGAGTAATA[-/C]CCTCAAATTCCAAAT	9972
rs770193542	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17650201	AGCAAGAAGAAACTG[C/G]ATGGGAGAGGACACT	9972
rs770223372	snp	G/T	1.64784e-05	0.00287035	missense	NUP153	GRCh38.p7	6:17675680	TGTAATGCAGGGGAT[G/T]CCAACATGGAAAAAT	9972
rs770225429	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696143	AAACAAACAAACCAA[C/T]CAACCCCAAAAAAGT	9972
rs770268817	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17616858	GGGTTCAAGTGATTC[C/T]CCTGCCTCAGCCTCC	9972
rs770271817	snp	A/G	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17624666	AAGTAGGTGGTGCAG[A/G]CTGAGAACCAGTGGG	9972
rs770273779	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17667024	TCTGGCTTTTTATTT[A/C]TTAGCACCCATTAAT	9972
rs770327586	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622216	GCACTTTAGGAGGCT[A/G]AGGTGGGTGGACTGC	9972
rs770365971	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660809	TCCAACAATTCCATT[C/T]CTAGATAAATACTCT	9972
rs770448969	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17684282	TAGCTAAATCTTCTG[G/T]ATAACTTATTGCAGC	9972
rs770450913	snp	A/G	1.70659e-05	0.00292107	missense	NUP153	GRCh38.p7	6:17629521	GCTGAGTTCGAAGAT[A/G]AGGAAGATGTGTCAA	9972
rs770484315	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17630861	TGACAAGATCAAAGT[A/C]TTGGTTTCATAATGC	9972
rs770546976	snp	C/T	1.6625e-05	0.00288309	intron-variant	NUP153	GRCh38.p7	6:17675806	ATTATGAATATACAA[C/T]TTAGAGCGATACACT	9972
rs770547550	snp	A/T	5.30894e-05	0.00515188	intron-variant	NUP153	GRCh38.p7	6:17637791	ATGAACGAAGGAGAG[A/T]GTGCAACGTTAGAGA	9972
rs770555341	in-del	-/TCTA			intron-variant	NUP153	GRCh38.p7	6:17691244	TCTACAAGTAAGCTC[-/TCTA]TCAAACACATGAAGC	9972
rs770558878	in-del	-/T			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615122	GCTTTAATATTAAAC[-/T]TTTCCTTATTATCCA	9972
rs770636877	snp	A/T	1.662e-05	0.00288266	intron-variant	NUP153	GRCh38.p7	6:17688386	GACAAAATATTCACA[A/T]TTTACTTACCTTCTG	9972
rs770636928	snp	A/C	1.77893e-05	0.00298234	intron-variant	NUP153	GRCh38.p7	6:17669043	GCTGAAAAAAAAAAA[A/C]AACACTATTAGAATA	9972
rs770642185	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17641131	ATATTTTTAAGGGGC[A/G]ATTTCTATTTACAGA	9972
rs770671243	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17644551	TTTGTGTTTATATTT[A/C]TTGGGTAAAATGCCC	9972
rs770689640	snp	A/G	1.64743e-05	0.00287	missense	NUP153	GRCh38.p7	6:17624701	AATGCTGTGGAAGAT[A/G]ATATAGATCCAAAGC	9972
rs770698436	snp	A/G	1.82327e-05	0.00301927	missense	NUP153	GRCh38.p7	6:17624806	GCAGATGGTGCTGAG[A/G]GTCCAGTTCCAAATA	9972
rs770704780	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17664249	GATGGTAATACAAAT[C/G]TTCTAAAATTTACCA	9972
rs770718107	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17640556	AAATATTAAATAAGG[G/T]TATATGGTTACATAA	9972
rs770738431	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17691069	ATTGCTTGGAACTGG[C/T]AGATGGAGGTTGCAG	9972
rs770742181	snp	A/T	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637254	GGCCTTTTGAATTTA[A/T]CTCCAAATCCTAAGG	9972
rs770748757	snp	C/T	3.29739e-05	0.00406028	synonymous-codon	NUP153	GRCh38.p7	6:17628758	ACTAAATGTGGACTT[C/T]GAAGAATTCTCATCT	9972
rs770751126	in-del	-/TT/TTT			intron-variant	NUP153	GRCh38.p7	6:17665717	TCAAACCTTTTACAG[-/TT/TTT]TTTTTTGTTTTTTTT	9972
rs770755972	snp	A/G	1.6651e-05	0.00288535	intron-variant	NUP153	GRCh38.p7	6:17661798	GCAAATAAAAAGAAA[A/G]TTAAAACAACTGATA	9972
rs770776800	in-del	-/AAA	9.24445e-05	0.00679807	intron-variant	NUP153	GRCh38.p7	6:17628637	AATAATAATAATAAT[-/AAA]AAAAAGTTAATACTT	9972
rs770786281	snp	C/T	1.65015e-05	0.00287237	missense	NUP153	GRCh38.p7	6:17629152	CCTGCAGAGGAAGAT[C/T]TGGGCAGTTCCTCTT	9972
rs770801516	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17619831	GGCCAGGCGCTGTGG[C/G]TCACACCTATAATCC	9972
rs770840964	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17622076	GGGAATGACCTTCAC[G/T]AGACTTTGTAGCATG	9972
rs770848336	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650509	GAGACAGAATGAGTT[C/T]AGAGAAGTCCATTGC	9972
rs770867773	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702219	CTAGAAAAATGACAC[C/T]ATTTCTGGCCGGGCG	9972
rs770885781	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676938	AGCAGCTGCTATGGA[A/G]TTGAGAAAACAGAGA	9972
rs770902776	in-del	-/TTT			intron-variant	NUP153	GRCh38.p7	6:17644180	TCTATGTCCTGACTC[-/TTT]TTATTTTTTAATCTA	9972
rs770902915	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17666407	GTAATCCCGGCTATT[C/G]AGGAGGCTGAGGCAG	9972
rs770903303	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17651823	TTGAGGTTAGGCATG[A/G]TAGCACATACCTGTA	9972
rs770924648	snp	G/T	1.65619e-05	0.00287762	intron-variant	NUP153	GRCh38.p7	6:17674902	CCTTCTATTGGAACC[G/T]ACCTGATAAGGTGTA	9972
rs770924806	snp	C/T	8.23621e-05	0.00641672	missense	NUP153	GRCh38.p7	6:17637357	TAAGGGCTCGCTTCA[C/T]ACAAGTTCCAGGTTT	9972
rs770927880	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17676836	GTAGGGAACTGTGCA[C/G]AGAGGGTCTCCCAGA	9972
rs770973507	snp	A/T	8.24002e-05	0.0064182	intron-variant	NUP153	GRCh38.p7	6:17647801	TATTCCTTGCTTGTT[A/T]CTTACAGATGATGGA	9972
rs770977863	in-del	-/A	4.98886e-05	0.00499418	intron-variant	NUP153	GRCh38.p7	6:17688629	ATGCCCTGTTGAGAG[-/A]AAAAACATATTATGA	9972
rs771012980	snp	A/G	1.64765e-05	0.00287019	missense	NUP153	GRCh38.p7	6:17629080	TTGTTCTCAGAGGTC[A/G]CTATGGTGTTAGCAG	9972
rs771013915	snp	C/T	1.64961e-05	0.00287189	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616064	GCAGGGCACCAGCTG[C/T]TGTTAAAATTGAGTA	9972
rs771030801	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698226	ATAGGGTAAACTTCG[C/T]TGCTGAATGGCATAG	9972
rs771048488	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658777	ATTTCTCAGATTGAG[A/G]CATGGGACAAAAAGT	9972
rs771051772	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638161	CTTTTAAGTGTTCCA[C/T]TGGCTACACCAAATG	9972
rs771062146	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17623057	ATCACTTGAACCCGG[C/G]AAGCGGAGGTTGCAG	9972
rs771081483	in-del	-/GAATAGATGGGG	1.80192e-05	0.00300154	intron-variant	NUP153	GRCh38.p7	6:17669054	AAAAAAACACTATTA[-/GAATAGATGGGG]AGTTATGAAAAATAC	9972
rs771085171	snp	A/G	1.64781e-05	0.00287033	missense	NUP153	GRCh38.p7	6:17675653	AATGCCGAGGATGTA[A/G]ATGGCTGACAGTGTA	9972
rs771091681	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17638072	ATGTATTATTGCCAT[A/C]CACATTTTGCTATAT	9972
rs771092681	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648790	CCTCGGCAATACAGC[A/G]AGACACCATCTCAAA	9972
rs771127372	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17640566	TAAGGGTATATGGTT[A/G]CATAAATTACATAAC	9972
rs771129251	snp	A/G	1.64819e-05	0.00287066	synonymous-codon	NUP153	GRCh38.p7	6:17665308	CAGAGATGGTTTAAA[A/G]TAAACACTTCGATTT	9972
rs771145122	snp	C/G	1.64993e-05	0.00287218	missense	NUP153	GRCh38.p7	6:17629414	TTTTGAATCCTCCCT[C/G]ATCTCCAAATTTAAA	9972
rs771180496	snp	A/G	1.70568e-05	0.0029203	missense	NUP153	GRCh38.p7	6:17629515	GAGGCTGCTGAGTTC[A/G]AAGATGAGGAAGATG	9972
rs771181912	snp	C/T	2.02871e-05	0.00318483	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706481	CCCCGCCGCCCGGCC[C/T]CGGCCCAAAAGTCCG	9972
rs771188253	snp	C/T	1.83159e-05	0.00302615	missense	NUP153	GRCh38.p7	6:17646151	CACTAAATGTAAATC[C/T]AATCTGTAAAGAGAA	9972
rs771237674	snp	A/T	4.95749e-05	0.00497845	missense	NUP153	GRCh38.p7	6:17626096	CACCACCAGCAGAAG[A/T]GGCTGGTGTACTTGA	9972
rs771260915	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17616780	TTTGAGACGGAGTCT[C/T]GCTCTCTTGCCCAGG	9972
rs771309957	snp	C/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614789	AAATGAATGTGTGTA[C/T]TTTCAACTTTTAAAA	9972
rs771325788	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17647975	AGTGACAAAAAAGAC[A/G]TTAAGCAAACTGATT	9972
rs771353076	snp	C/T	1.64874e-05	0.00287113	missense	NUP153	GRCh38.p7	6:17675569	GTAGTTGAGATGTTA[C/T]CATCATCATGCTGAG	9972
rs771364626	snp	C/T	1.65685e-05	0.00287819	missense	NUP153	GRCh38.p7	6:17637723	AAACTACTGGGCTTG[C/T]TGCGGTGGGCTGAGC	9972
rs771367950	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17673462	TTTGTACCCTGAAAA[A/T]TGAACTCTCTCAAAA	9972
rs771370566	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671472	TTTAAATTATGAACT[C/T]AATTCACTGAAAAGA	9972
rs771381948	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17665850	CCACCACACCCGGCT[A/G]ATTTTTTTGGTTTTT	9972
rs771383060	in-del	-/TTTGTTTG	0.000170771	0.00923885	intron-variant	NUP153	GRCh38.p7	6:17616746	AAAATGATAGGTTTT[-/TTTGTTTG]TTTGTTTGTTTTTTG	9972
rs771384178	snp	A/C	3.35121e-05	0.00409328	intron-variant	NUP153	GRCh38.p7	6:17624539	ACCCATACAGATACT[A/C]ACAGCATCACAGCAC	9972
rs771387887	snp	C/G	2.25813e-05	0.00336008	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706415	GCCGCTTCCCGCTCC[C/G]GGGCGGGTAAGGGGG	9972
rs771393007	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17618364	CTGAGACAAAAATAA[C/T]AAAAGCAATTTTGGG	9972
rs771412208	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17678072	CATTAAATATGATTC[C/T]GGGCTGGGCACAGTG	9972
rs771412827	in-del	-/AAT			intron-variant	NUP153	GRCh38.p7	6:17628620	ACTTGTAAAAAAAAA[-/AAT]AATAATAATAATAAT	9972
rs771413037	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17683880	AGATGTTTGTCCCTC[C/T]AAATCCTATGCTGAA	9972
rs771416174	snp	A/G	1.64776e-05	0.00287028	missense	NUP153	GRCh38.p7	6:17628955	CGTTGCCAAAAGAGA[A/G]TCCTCCTTTGGTGGC	9972
rs771423943	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17643740	GAACCAACGGTGTCA[A/G]AGTGAGAACACACAA	9972
rs771452031	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664806	ATCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG	9972
rs771458324	snp	C/T	3.29701e-05	0.00406005	missense	NUP153	GRCh38.p7	6:17616663	TTGTGAAGTTGAAAT[C/T]TGTAGTGCTGCTGCC	9972
rs771491612	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695070	GTGTCCTTGGATCAT[A/G]CAATTCAAAGCTTCT	9972
rs771506358	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17671783	GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA	9972
rs771522367	snp	C/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705785	CCACTTTCCATGTAA[C/G]AGCGCCCCCCACAAC	9972
rs771563876	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17630417	GGAATCCCAGCACTT[G/T]GGGAGGCCAAGGCGG	9972
rs771566703	snp	A/G	1.71387e-05	0.00292729	missense	NUP153	GRCh38.p7	6:17624791	CCAAATGCTGGACTG[A/G]CAGATGGTGCTGAGG	9972
rs771575249	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17694373	TAAAGAAATAAAGGA[C/T]AGGAGCTGGGCCCGG	9972
rs771581179	snp	A/G			upstream-variant-2KB, nc-transcript-variant, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707283	AGCTAATGATTTAAG[A/G]AGGAGGAAAAAAAAA	9972
rs771597906	snp	A/C	1.64735e-05	0.00286993	missense	NUP153	GRCh38.p7	6:17637624	GGAGTAGACATGTAT[A/C]ACACTGCCATGATGA	9972
rs771616501	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17651328	CAAAACCAATAAAAA[C/G]AGAATTATAATAATA	9972
rs771625161	snp	C/G	1.6717e-05	0.00289106	missense	NUP153	GRCh38.p7	6:17637746	GGCTGAGCAGCAACA[C/G]AATCTATCTTCGGCG	9972
rs771649447	in-del	-/TG			intron-variant	NUP153	GRCh38.p7	6:17656344	CTGGGTGAAGAATCC[-/TG]TGACACAAAATTGGC	9972
rs771652679	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17631575	TTTAGCTACAACTTA[C/T]AAGTAAGAAGATGAA	9972
rs771656921	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704873	CAAGCCATTCTCCTG[C/T]CTCAGCCTCCCAAGT	9972
rs771657545	snp	A/T	0.000899425	0.0211873	intron-variant	NUP153	GRCh38.p7	6:17674862	AGTTAAAGTGTAAAA[A/T]AAAAGAAAAAAAAAG	9972
rs771668299	snp	A/G	1.64735e-05	0.00286993	missense	NUP153	GRCh38.p7	6:17624692	GTGGGAAATAATGCT[A/G]TGGAAGATGATATAG	9972
rs771669087	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643685	AGTAATCATGACTTC[C/T]ACATTTTCAATTAGC	9972
rs771694596	snp	C/T	1.65195e-05	0.00287393	intron-variant	NUP153	GRCh38.p7	6:17661642	AAGAGTATATGAGTA[C/T]ACAACCCTACCTCCT	9972
rs771721743	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694165	GCTCCAAGAAGGCAG[A/G]AACTTGTTCACTGCT	9972
rs771747431	snp	C/G	1.65042e-05	0.0028726	missense	NUP153	GRCh38.p7	6:17661766	GCAAACTGAAATTTG[C/G]ATATGAAAAGCCACT	9972
rs771750542	snp	C/T	1.64808e-05	0.00287057	synonymous-codon	NUP153	GRCh38.p7	6:17624589	TGTTCCAGAGCCAAA[C/T]GCAGACTGACTAGGT	9972
rs771766620	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17651652	CAGTAAGAGTGGCTG[G/T]ATTAATACCAAAGTA	9972
rs771771320	snp	C/T	1.64822e-05	0.00287068	missense	NUP153	GRCh38.p7	6:17675695	TCCAACATGGAAAAA[C/T]TCAGATGGCTCCGAT	9972
rs771839990	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17621154	GAAATGCAAATCAAA[A/C]CCACAATGAGGTAGC	9972
rs771840762	snp	A/C	1.64768e-05	0.00287021	missense	NUP153	GRCh38.p7	6:17629004	AGCTTCTGATGTCTT[A/C]CATGTGAAAGGAGCC	9972
rs771847308	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17654280	CAACTCCTTAAGGCA[A/C]ACACTTGTCCACACT	9972
rs771890729	snp	C/T	1.65669e-05	0.00287805	intron-variant	NUP153	GRCh38.p7	6:17669550	TCTAACTGGTGCCTG[C/T]AAAGTAAACCCTATA	9972
rs771900294	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642702	ACATATGAAAAAGCA[C/T]TGAAACCAGTACTCA	9972
rs771905938	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17639146	GCAGTGGTTCGATCT[C/T]GGTTCACTGCAACCT	9972
rs771923677	in-del	-/GGGATGGGGAGAGGA			intron-variant	NUP153	GRCh38.p7	6:17641203	TGTAAGTTTCTGTGT[-/GGGATGGGGAGAGGA]GGGATGGAACAAAAG	9972
rs771924442	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17622158	AGAGTCAAGAGTTTT[C/G]TAACATCTTGGCTGG	9972
rs771934902	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	NUP153	GRCh38.p7	6:17637238	CTCCCAAGATCCAAT[A/G]GGCCTTTTGAATTTA	9972
rs771988493	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17659721	CGTGATCCGCCCGCC[C/T]TGGCCTCCCAAAGTG	9972
rs771995444	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17646247	GAGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTGC	9972
rs772059341	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700733	GCAAACAATGACCTG[C/T]GGGCTGGGCCAAATT	9972
rs772067401	snp	A/G	1.64806e-05	0.00287054	missense	NUP153	GRCh38.p7	6:17688590	GGCACAATATTCTTA[A/G]CAGATTCTGTAACCC	9972
rs772068516	in-del	-/GG			intron-variant	NUP153	GRCh38.p7	6:17701832	GCAAGACTCTGTCTC[-/GG]GGGGGGGGGGGGAAA	9972
rs772070516	snp	G/T	1.648e-05	0.0028705	missense	NUP153	GRCh38.p7	6:17625941	TGCTAGTTTGCTATC[G/T]TGAGAAAATAGCAAA	9972
rs772087195	snp	A/G	1.64871e-05	0.00287111	synonymous-codon	NUP153	GRCh38.p7	6:17665290	GAATTCACCAGAAGG[A/G]GTCAGAGATGGTTTA	9972
rs772094251	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699665	ACATGGTGAAACCCC[A/G]TGTCTACTAAAAATA	9972
rs772110884	in-del	-/ATTAAT	3.31917e-05	0.00407367	intron-variant	NUP153	GRCh38.p7	6:17675785	TCTTAAAAGAAAAGC[-/ATTAAT]ATTATGAATATACAA	9972
rs772140919	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658562	CAAGGACCAATTGAG[A/G]GCAATCATCAAAGCT	9972
rs772165850	snp	A/G	1.64999e-05	0.00287222	intron-variant	NUP153	GRCh38.p7	6:17647784	AATCAGTAAATATAT[A/G]CTATTCCTTGCTTGT	9972
rs772195966	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17647575	AGAATTAAGGAAATC[C/T]AGTTGTTTGCATTTT	9972
rs772229077	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17655877	CAAAACAACTATATA[A/G]TTGTGTATCCAAACC	9972
rs772241964	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17696279	GTAAAAAGAGTCTGA[A/C]AAGAGGAAAAACGGT	9972
rs772250481	snp	A/C	1.66081e-05	0.00288163	missense	NUP153	GRCh38.p7	6:17629323	GAAACTCCAAATTTA[A/C]AATCTCCTATTGGTT	9972
rs772269468	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17664406	AAGAAACAGAAACCA[A/G]TGTGGCCAGGGTGAG	9972
rs772273751	snp	A/G	3.31131e-05	0.00406884	missense	NUP153	GRCh38.p7	6:17675357	ATGAAGTGTTCTTTG[A/G]AACAGTTATATCTGA	9972
rs772291122	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697267	GTCAAAAATGCCACT[A/G]AGATTTAGACTAATT	9972
rs772306509	snp	A/C/T	3.29474e-05	0.00405867	missense	NUP153	GRCh38.p7	6:17637593	GCTATGCATTTGTTG[A/C/T]CTGTAACTTTGTTCT	9972
rs772341764	snp	C/T	2.89817e-05	0.00380658	intron-variant	NUP153	GRCh38.p7	6:17646030	ATCTACTGTATGCAA[C/T]TGTTTGTATGTTAAA	9972
rs772341892	in-del	-/C	3.55142e-05	0.00421377	intron-variant	NUP153	GRCh38.p7	6:17669041	GGCTGAAAAAAAAAA[-/C]AAAACACTATTAGAA	9972
rs772365817	snp	A/G	5.29535e-05	0.00514528	intron-variant	NUP153	GRCh38.p7	6:17665203	TACTTATTCTAATCA[A/G]TATTCAAAGACTGGT	9972
rs772376327	snp	A/C/G	4.94192e-05	0.00497067	synonymous-codon	NUP153	GRCh38.p7	6:17637493	TGTCCCTGATGCAGA[A/C/G]AGAGTTGTTTTGCCA	9972
rs772378056	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693359	TTAAACACTAGATAT[C/T]AGAGAATGGGAGTAA	9972
rs772441535	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17692297	CTTAATAGAGGAACA[G/T]TGAGACAGAGACATT	9972
rs772458136	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17625539	CGTCTCGAAAGAAAA[C/T]AAAAACAAAAAACAA	9972
rs772458556	snp	C/G	1.71687e-05	0.00292986	missense	NUP153	GRCh38.p7	6:17637770	TTCGGCGATGCGAAA[C/G]CTACAATGAACGAAG	9972
rs772458960	snp	C/T	1.6477e-05	0.00287024	missense	NUP153	GRCh38.p7	6:17649210	GTGATGGAGAGGAAG[C/T]TGTGATCTCAGGGGA	9972
rs772459277	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17670564	TGGCTAGCACCTGCA[A/G]TATGATGTTAAACAG	9972
rs772507352	snp	C/T	3.295e-05	0.00405881	missense	NUP153	GRCh38.p7	6:17628859	CAAAAACTAGGGAAG[C/T]AGAAGTGACAGGCTC	9972
rs772531480	in-del	-/CTCTTT			intron-variant	NUP153	GRCh38.p7	6:17618560	TGGAAGTTAAAATCT[-/CTCTTT]TTTTTTTTTTTTTTT	9972
rs772532233	in-del	-/TTCAGATACT			downstream-variant-500B	NUP153	GRCh38.p7	6:17614885	TCTATATGTTGTGCA[-/TTCAGATACT]TTCAGATACTTTCCC	9972
rs772541822	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17687926	GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC	9972
rs772543268	snp	A/T	1.65611e-05	0.00287755	missense	NUP153	GRCh38.p7	6:17649297	ATACTGGAACTTCCA[A/T]TTCCTAAAACATAAC	9972
rs772561822	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17671157	TTCCCAGGATAAACC[C/T]CACTTGATCATGATG	9972
rs772591039	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707533	TTGTGAGGAGCAGAC[A/G]TGATCATCTATGGAG	9972
rs772597456	snp	A/C/T	3.46995e-05	0.00416518	intron-variant	NUP153	GRCh38.p7	6:17668929	GAACTTTAAACACAA[A/C/T]AAAATTGTAGACAGT	9972
rs772622561	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705370	CTCATTTACAATTAG[A/G]ATAATCCTTTTTTAT	9972
rs772642489	snp	C/T	1.71073e-05	0.00292461	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632629	TTACCATCACCTTTA[C/T]TTTTATTTTTTTGGC	9972
rs772652824	snp	A/T	3.31472e-05	0.00407093	missense	NUP153	GRCh38.p7	6:17669336	GGAATTCTTTTTGCA[A/T]CCTGTTAAAGTTGAA	9972
rs772666585	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619904	GGAGTTCGAGACCAG[C/T]GTGGCCAACATGGCA	9972
rs772695508	in-del	-/C	1.70912e-05	0.00292324	intron-variant	NUP153	GRCh38.p7	6:17625785	CATCCAATTACAATG[-/C]ATTTTTTCTTTTGTA	9972
rs772707964	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17703734	GTTTCTGCCAATATT[A/T]AATAGCACCTACAGT	9972
rs772717815	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17631585	ACTTATAAGTAAGAA[A/G]ATGAAATATCTGTCT	9972
rs772751209	snp	A/G	1.77995e-05	0.00298319	intron-variant	NUP153	GRCh38.p7	6:17616509	TAACTTCTCCATTTC[A/G]ATAAAAAATTCTCTT	9972
rs772762251	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672868	GAACCTTGACCAATA[C/T]CTCATACCACACACA	9972
rs772771976	snp	C/T	3.44863e-05	0.00415235	synonymous-codon	NUP153	GRCh38.p7	6:17629529	CGAAGATGAGGAAGA[C/T]GTGTCAAAGCCTACA	9972
rs772805488	snp	C/T	1.65614e-05	0.00287757	splice-acceptor-variant	NUP153	GRCh38.p7	6:17661780	GGATATGAAAAGCCA[C/T]TGGCAAATAAAAAGA	9972
rs772856480	snp	G/T			downstream-variant-500B	NUP153	GRCh38.p7	6:17614757	TAACTTACCAAGGAA[G/T]ATAGAAGCACAAAGA	9972
rs772859366	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705010	GATCCACCCGCCTCG[A/G]CCTCCCAAAGTGCTG	9972
rs772869138	snp	A/G	1.64768e-05	0.00287021	missense	NUP153	GRCh38.p7	6:17629006	CTTCTGATGTCTTAC[A/G]TGTGAAAGGAGCCAC	9972
rs772917788	snp	C/G	6.59196e-05	0.00574068	missense	NUP153	GRCh38.p7	6:17624591	TTCCAGAGCCAAATG[C/G]AGACTGACTAGGTTG	9972
rs772921760	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17666440	GAATCGTTTGAACCC[A/G]GAGGCAGAGCTTTCA	9972
rs772968245	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642726	GTACTCAAACAAATA[C/T]ACATACACATATGTT	9972
rs772981842	snp	G/T	3.31796e-05	0.00407292	intron-variant	NUP153	GRCh38.p7	6:17669554	ACTGGTGCCTGTAAA[G/T]TAAACCCTATATTAT	9972
rs773000374	snp	A/G	1.65157e-05	0.0028736	intron-variant	NUP153	GRCh38.p7	6:17661643	AGAGTATATGAGTAT[A/G]CAACCCTACCTCCTC	9972
rs773019373	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643713	AGCTTTTTTAAATGA[C/T]AGAAGTGGTGAGAAC	9972
rs773047804	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17684794	ACTAATTAGCCTAAT[G/T]TCAATACTGTCAGAG	9972
rs773058904	in-del	-/TC			intron-variant	NUP153	GRCh38.p7	6:17697211	AAATCCACTGGGTAT[-/TC]TCTCTCCAAGAAAGA	9972
rs773079670	snp	A/G/T			intron-variant	NUP153	GRCh38.p7	6:17677168	AGCTTGGAGGCTAAG[A/G/T]CCCACCACATTGGGA	9972
rs773086006	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660791	GTGGATCATCCCCTA[C/T]AATCCAACAATTCCA	9972
rs773125546	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17690877	GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	9972
rs773129814	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17678549	AACGCTGAATGATTA[C/T]TTGCATTCCTTGATT	9972
rs773178616	snp	C/G	1.64768e-05	0.00287021	synonymous-codon	NUP153	GRCh38.p7	6:17629076	GCTCTTGTTCTCAGA[C/G]GTCACTATGGTGTTA	9972
rs773180250	snp	C/T	1.64811e-05	0.00287059	missense	NUP153	GRCh38.p7	6:17669494	GTTGAACTGGTCACA[C/T]CGTAAGATTGTGCAC	9972
rs773184726	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17679677	GAACAGGAGGTGGGA[C/G]GTAGTTTCTCCTTCA	9972
rs773204875	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17618732	ACCACGCCTGGCTAA[-/T]TTTTTTGTATTTCTT	9972
rs773209903	snp	C/T	8.2392e-05	0.00641788	missense	NUP153	GRCh38.p7	6:17675687	CAGGGGATTCCAACA[C/T]GGAAAAATTCAGATG	9972
rs773214724	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17621176	TGAGGTAGCATTTCA[A/C]CTCTTAGAATGGCTA	9972
rs773215443	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17689789	CTCTGCCTCCCAAAG[C/T]GCTGGGATTACAAGC	9972
rs773263607	snp	A/C	1.64969e-05	0.00287196	missense	NUP153	GRCh38.p7	6:17629404	GACACACCTATTTTG[A/C]ATCCTCCCTGATCTC	9972
rs773289229	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657467	TACTTGGGAGGCTGA[A/G]ACATGAGAATCACTT	9972
rs773313577	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679792	AAAAAGAAAACAGCC[A/G]TTCTTCGGTGCTCTC	9972
rs773324759	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17618298	CACTCATAACAACTA[A/C]AGGTAGCCAAGGAGT	9972
rs773339963	snp	A/G	1.64849e-05	0.00287092	missense	NUP153	GRCh38.p7	6:17665298	CAGAAGGAGTCAGAG[A/G]TGGTTTAAAATAAAC	9972
rs773352803	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17697364	ATTGTGAATACATTA[A/G]CTTTTCAAATTATAT	9972
rs773370651	snp	C/T	4.94205e-05	0.0049707	missense	NUP153	GRCh38.p7	6:17688510	GCCAGCGTGGAACCT[C/T]GCTTGTGTCTGTTGA	9972
rs773393894	in-del	-/C	5.37172e-05	0.00518225	intron-variant	NUP153	GRCh38.p7	6:17669045	GAAAAAAAAAAAAAA[-/C]CACTATTAGAATAGA	9972
rs773395460	in-del	-/ACA			intron-variant	NUP153	GRCh38.p7	6:17684877	GCAGCTGGAACACAC[-/ACA]ACATTTACTGATTAA	9972
rs773444869	snp	A/C/T	0.000114608	0.00756919	intron-variant	NUP153	GRCh38.p7	6:17632864	AAAAAAAAAAAAAAA[A/C/T]GGGGAGTGGGGGGAG	9972
rs773445182	snp	C/G	1.77012e-05	0.00297494	missense	NUP153	GRCh38.p7	6:17646132	GCTGTTTTTGCAACA[C/G]GCACACTAAATGTAA	9972
rs773469934	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692499	TGCCTGGGTGACAGA[A/G]ACCCTGTTTCTAAAA	9972
rs773482563	snp	C/G	1.65693e-05	0.00287826	missense	NUP153	GRCh38.p7	6:17675360	AAGTGTTCTTTGAAA[C/G]AGTTATATCTGAAAC	9972
rs773497104	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17646282	GCGCAATCCTGGCTC[A/G]CTGCAACCTCCGCCT	9972
rs773509912	snp	C/T	4.06934e-05	0.00451055	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706404	GCGGAGCCTCCGCCG[C/T]TTCCCGCTCCGGGGC	9972
rs773521912	in-del	-/GGAGAAT			intron-variant	NUP153	GRCh38.p7	6:17690259	CGGGAGGCTGAGGCA[-/GGAGAAT]GGCGTGAACCCGGGT	9972
rs773570751	snp	A/C	1.64868e-05	0.00287109	missense	NUP153	GRCh38.p7	6:17675245	GGGGAAAGTGTTCCA[A/C]AGGCAGACAAGTTGA	9972
rs773581848	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658572	TTGAGAGCAATCATC[A/G]AAGCTGATCCTTTTA	9972
rs773603330	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17693368	AGATATTAGAGAATG[A/G]GAGTAAAGAGAGGTC	9972
rs773617109	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636787	CTTCCCTGTAAATGA[C/T]CACTAGCTATCCTGA	9972
rs773654691	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17682142	AGTGAGTCACACACG[G/T]TTTTGGTTTCCCAGT	9972
rs773668057	snp	C/G			downstream-variant-500B	NUP153	GRCh38.p7	6:17614907	ACTTTCAGATACTTT[C/G]CCTTTCTCTTAGGAG	9972
rs773670952	snp	G/T	1.66034e-05	0.00288122	missense	NUP153	GRCh38.p7	6:17629338	AAATCTCCTATTGGT[G/T]TAGAAAATTTAAAGC	9972
rs773674723	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648957	TCTCTATGGTATTGC[A/G]TAAGAGTTGAGGAAC	9972
rs773679513	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17625604	AATTAGAAAAATTGC[C/T]CCCAAGAGGTAAATA	9972
rs773688472	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705699	TAAAATCTAAGCCAA[C/T]GCTCTCAAGACGAGG	9972
rs773699213	snp	A/G	1.6537e-05	0.00287545	intron-variant	NUP153	GRCh38.p7	6:17661637	ACCTCAAGAGTATAT[A/G]AGTATACAACCCTAC	9972
rs773715899	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676684	TTCAGACAGTGGAAA[A/G]CAGCACAAAAAAAAA	9972
rs773764262	snp	A/C	1.64819e-05	0.00287066	missense	NUP153	GRCh38.p7	6:17675592	ATGCTGAGAGGTAGA[A/C]TCTTTAATTTCCTTT	9972
rs773771029	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17664553	AGGAATTAGAATTAA[C/T]TTTCTTAGATGGGAT	9972
rs773777225	snp	C/T	4.94482e-05	0.00497209	missense	NUP153	GRCh38.p7	6:17616656	CTGTTGTTTGTGAAG[C/T]TGAAATTTGTAGTGC	9972
rs773784892	snp	C/T	1.66247e-05	0.00288307	synonymous-codon	NUP153	GRCh38.p7	6:17637733	GCTTGTTGCGGTGGG[C/T]TGAGCAGCAACAGAA	9972
rs773838890	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17682015	GAGTTCAAGACCAGC[A/C]TGGGCAACACAGTGA	9972
rs773861853	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17653207	GCAGTGAGCCAAGAT[C/T]GTGCTACTGCACTCC	9972
rs773910257	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17637654	ACCCAGCTTTTAAAC[C/T]CTCCCCAAACCCAAT	9972
rs773919079	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17703842	ACAAGAAGCAAAAGT[A/G]TTTTAGATAAGGGGC	9972
rs773926129	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17680718	GATTAATATCCAGAA[C/T]ATAAAAAGTACTCCA	9972
rs773942508	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17647200	TAGAAAATGACATAT[G/T]AAAATAATATAAACA	9972
rs773944419	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17625554	CAAAAACAAAAAACA[A/G]AGCTTAGAAAAATTA	9972
rs773979604	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17642598	AATGGTAATGTGACA[C/T]GGTTCAACTACTGTG	9972
rs773996421	in-del	-/AG	1.86572e-05	0.00305422	frameshift-variant	NUP153	GRCh38.p7	6:17624811	TGGTGCTGAGGGTCC[-/AG]TTCCAAATACAAAGG	9972
rs774003271	snp	C/G	0.000202163	0.0100519	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17651843	ACATACCTGTAATCT[C/G]AGCACTTTGAGAGGC	9972
rs774013222	snp	A/G	3.29527e-05	0.00405898	missense	NUP153	GRCh38.p7	6:17628996	TCTTTTTTAGCTTCT[A/G]ATGTCTTACATGTGA	9972
rs774035265	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17627967	AAAACTTCTTATCTT[A/C]TAGGCCACTCCTATC	9972
rs774053723	snp	C/T	1.65002e-05	0.00287225	missense	NUP153	GRCh38.p7	6:17629426	CCTGATCTCCAAATT[C/T]AAAATTTCCAGTGCT	9972
rs774054908	snp	C/T	6.59011e-05	0.00573988	synonymous-codon	NUP153	GRCh38.p7	6:17628890	TTGCTGTTTCTCTTC[C/T]GTCCTTCCCAAAACA	9972
rs774067262	in-del	-/GGGCGTGGTGGT			intron-variant	NUP153	GRCh38.p7	6:17698595	TACAAAAAATTAGCG[-/GGGCGTGGTGGT]GGGCACCTGTAGTCC	9972
rs774114606	snp	C/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17688500	TTATTTTCTGGCCAG[C/T]GTGGAACCTCGCTTG	9972
rs774116743	snp	C/T	1.65482e-05	0.00287643	intron-variant	NUP153	GRCh38.p7	6:17669381	AAGATTTTTCAATAA[C/T]ATCAAGTTTTGTTAC	9972
rs774133001	snp	A/G	1.64795e-05	0.00287045	missense	NUP153	GRCh38.p7	6:17669476	TGCAATATTCGCCGA[A/G]CTGTTGAACTGGTCA	9972
rs774160977	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17659714	TTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC	9972
rs774184240	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704538	CTAATCTTAAATCTG[C/T]TCGCAAATACCCCTT	9972
rs774188125	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17620938	AATTTGTTGAAAGGG[A/G]AAAAAAGTTTGCTAA	9972
rs774238585	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17677733	TAATTTTTTTTTTCC[-/TT]TTTTTTTTTTTTTTT	9972
rs774243544	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17689491	TGACATTTCACTACA[A/G]CAAATGTTGGCTGAA	9972
rs774247886	snp	A/G	3.44062e-05	0.00414752	intron-variant	NUP153	GRCh38.p7	6:17637144	TACTCCATAAAGCCA[A/G]AAACATACCTGGTTT	9972
rs774269038	in-del	-/G	0.000114607	0.00756903	intron-variant	NUP153	GRCh38.p7	6:17632864	AAAAAAAAAAAAAAC[-/G]GGGGAGTGGGGGGAG	9972
rs774281487	snp	G/T	2.84353e-05	0.00377053	intron-variant	NUP153	GRCh38.p7	6:17624855	GCCCAAAGAAACACT[G/T]AAGTCACCATGGTGG	9972
rs774298937	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17658717	TGAAAATTTAAAAAA[C/T]TGTTTTGAAGTGTCG	9972
rs774310922	snp	C/G/T	3.29518e-05	0.00405894	missense	NUP153	GRCh38.p7	6:17688431	GGCTCAGGTGTGATT[C/G/T]TCCCATCAGTAATAT	9972
rs774316426	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674525	TGTAATCCTAACACT[C/T]TGGGAGGCCGGGGTG	9972
rs774351598	in-del	-/TC			intron-variant	NUP153	GRCh38.p7	6:17645278	ATTCTATGTTTTAAT[-/TC]TCTGATTATTCATTC	9972
rs774353310	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17657594	ACCTGGTGCCATGGT[A/G]TTGGCTTCTGTGCTC	9972
rs774366652	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17698461	TAGCTGGGAGCAGCC[A/G]GGCGTGGTGGCTCAC	9972
rs774368242	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17631448	GGCTTTTAGTATATT[A/C]ATCACCCAAATAATG	9972
rs774385401	in-del	-/C	1.66073e-05	0.00288156	intron-variant	NUP153	GRCh38.p7	6:17647935	TATTAAGAAATGATA[-/C]AAAAAGAGCTTTTTA	9972
rs774390406	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17696201	TGGAGAGGTACCTCC[C/T]TGACTGGCAGTTTTT	9972
rs774419730	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17689540	TATTACGGTAACTTC[-/T]TTTTTTTTTTTTTGA	9972
rs774438597	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648145	AGTAAAGTAACATCT[A/G]TAAGAATATGTTCAG	9972
rs774475517	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17665724	CTTTTACAGTTTTTT[-/G]TTTTTTTTTTTTAAG	9972
rs774482892	snp	C/G	1.64885e-05	0.00287123	synonymous-codon	NUP153	GRCh38.p7	6:17675331	AGCTTCTGGGGACCA[C/G]AGAGGTGGCAATGAA	9972
rs774487915	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	NUP153	GRCh38.p7	6:17637475	AAATTTGTCTCCAAA[A/G]CCTGTCCCTGATGCA	9972
rs774487966	snp	C/T	1.65255e-05	0.00287445	missense	NUP153	GRCh38.p7	6:17629179	TCTTTCTTTTCTTCC[C/T]GTCCAAGATTAGATA	9972
rs774511020	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699642	AGAAGTTTGAGACCA[C/T]CACACCAACATGGTG	9972
rs774518107	in-del	-/TCTCTTT			intron-variant	NUP153	GRCh38.p7	6:17618559	GTGGAAGTTAAAATC[-/TCTCTTT]TTTTTTTTTTTTTTT	9972
rs774565228	snp	C/T	3.29598e-05	0.00405941	missense	NUP153	GRCh38.p7	6:17662043	GTTCTCTATTTTGTC[C/T]GGGTGTCATATTTTT	9972
rs774583396	snp	G/T	3.55e-05	0.00421293	intron-variant	NUP153	GRCh38.p7	6:17665191	ATTATTTAGTCTTAC[G/T]TATTCTAATCAATAT	9972
rs774586830	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17667334	AGATAATAATTTATC[A/G]ATATCTTAGTCATTG	9972
rs774597784	snp	G/T	1.64863e-05	0.00287104	missense, intron-variant	NUP153	GRCh38.p7	6:17640025	TCTTCAGGTGGTGTC[G/T]TCTTACAATTTGTAC	9972
rs774599182	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17703420	ACCTCTCATTGTTTC[C/T]TACTCCAACTTTCTG	9972
rs774609298	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17640536	TATTGAAAACCTATA[C/T]GGTAAAATATTAAAT	9972
rs774635380	in-del	-/TC			intron-variant	NUP153	GRCh38.p7	6:17618561	GGAAGTTAAAATCTC[-/TC]TTTTTTTTTTTTTTT	9972
rs774637940	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17656734	ATTGGCCTTAAGGTA[G/T]TATGTTTATTAGGAA	9972
rs774666858	snp	C/G	1.64746e-05	0.00287002	missense	NUP153	GRCh38.p7	6:17647838	ACATTTGCCTCAGTA[C/G]ATTTTACGATTGGAG	9972
rs774683812	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17628575	ATTAATTGACTTGCT[A/G]CATCTGTCAAGGCAA	9972
rs774687570	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17633250	TCTAAGACATAAGAT[A/G]TAAATTGTAGGCAAT	9972
rs774708827	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687016	AAGAATAAGGACATG[C/T]AACAGAAAATCCTCC	9972
rs774717023	snp	C/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637375	AAGTTCCAGGTTTCG[C/G]TGTTTCACAGGCTAC	9972
rs774737065	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627620	TGTGCTTCAGCCTCC[C/T]GACTAGTTGGGATTA	9972
rs774758090	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702528	CAAAACAAAAAAAAT[C/T]AGCCGTTTGTGGTGG	9972
rs774778606	snp	C/T	5.14672e-05	0.00507257	intron-variant	NUP153	GRCh38.p7	6:17649128	AGAATTAAGAAAGAA[C/T]AAATGTCACCTGTAT	9972
rs774805927	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666911	AACTCTTCCCTAAAA[C/T]CTCTTCGCAAATGTG	9972
rs774808982	snp	A/G			synonymous-codon	NUP153	GRCh38.p7	6:17646110	ACTACTAGAACCAGA[A/G]AGTTCTGCTGTTTTT	9972
rs774810622	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17635638	AACTGGGTTCAAGCA[A/G]TATACCCGCCTTGGC	9972
rs774856841	snp	A/G	1.64836e-05	0.0028708	missense	NUP153	GRCh38.p7	6:17669446	GCTAAAGGGCTTGAC[A/G]TCTTCTCTAAAGACT	9972
rs774868378	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634743	TGCCTGGTCACATTA[C/T]ATACATCTGAATGTT	9972
rs774889438	snp	A/G	2.34436e-05	0.00342363	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706417	CGCTTCCCGCTCCGG[A/G]GCGGGTAAGGGGGCG	9972
rs774906309	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17663151	AGAGAAAAAGATAGA[C/G]CAAATGTAGTAAAAT	9972
rs774920790	snp	A/G	1.85906e-05	0.00304877	intron-variant	NUP153	GRCh38.p7	6:17616487	CATGCACATACCCTT[A/G]CCAATGTAACTTCTC	9972
rs774932372	snp	C/T	4.94703e-05	0.0049732	missense	NUP153	GRCh38.p7	6:17616666	TGAAGTTGAAATTTG[C/T]AGTGCTGCTGCCAAA	9972
rs774959417	snp	A/T	0.000288143	0.0119995	intron-variant	NUP153	GRCh38.p7	6:17628628	AAAAAAAAATAATAA[A/T]AATAATAATAAAAAG	9972
rs774968492	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692176	AAAACATAACTGGTC[A/G]AAGTGGATATAATAA	9972
rs774973560	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17623450	TACAATGGTGGTAGG[A/C]TATGAATTGGCAGAA	9972
rs775008638	snp	C/T	1.65282e-05	0.00287469	missense	NUP153	GRCh38.p7	6:17628736	CAGATGGTTTTGTCA[C/T]ACTAAAACTAAATGT	9972
rs775010617	snp	A/T	1.64803e-05	0.00287052	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616096	AACACCAATGTGACC[A/T]TTATTTCCTGCGTCT	9972
rs775015436	in-del	-/AAAC			intron-variant	NUP153	GRCh38.p7	6:17689409	CAAAACAAAACAAAT[-/AAAC]AAACAAAAAAAAACA	9972
rs775024766	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635610	CTTCACCATGCTGCT[C/T]GGGCTGGTCTTAAAC	9972
rs775043981	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17640726	GGCTTAAGCAATCCT[C/T]CCACCTTAGCCTCTC	9972
rs775056435	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17702364	TACAAAAAATTAGCC[A/G]GACGTGGTGGCAAGG	9972
rs775087132	snp	A/G	7.61035e-05	0.00616814	intron-variant	NUP153	GRCh38.p7	6:17632849	TACTGAACTTCCTAA[A/G]AAAAAAAAAAAAAAC	9972
rs775088751	snp	A/C	1.64773e-05	0.00287026	synonymous-codon	NUP153	GRCh38.p7	6:17628791	GGTTTGCTCTGAATT[A/C]CCAAAGGAAAACACT	9972
rs775108897	snp	C/T	0.000115337	0.00759312	missense	NUP153	GRCh38.p7	6:17649254	GTAGGCAGTGAAGAA[C/T]TGGTGATCGGTAGAG	9972
rs775137931	snp	C/G	1.64757e-05	0.00287012	missense	NUP153	GRCh38.p7	6:17628877	AAGTGACAGGCTCTT[C/G]CTGTTTCTCTTCTGT	9972
rs775145197	snp	A/C	1.64827e-05	0.00287073	missense, intron-variant	NUP153	GRCh38.p7	6:17640002	CAGGTCTAAAAGGAC[A/C]CTCACAATCTTCAGG	9972
rs775147027	in-del	-/T	1.65064e-05	0.00287279	intron-variant	NUP153	GRCh38.p7	6:17647781	TGAAATCAGTAAATA[-/T]ATACTATTCCTTGCT	9972
rs775153651	snp	C/T	1.68471e-05	0.00290228	intron-variant	NUP153	GRCh38.p7	6:17649334	CATGATATATTTCAT[C/T]TTTCACATCATTCTT	9972
rs775161877	snp	G/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17637511	AGTTGTTTTGCCACT[G/T]TTATTTGGTGTTTCA	9972
rs775203397	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679938	AGCATTGTTGCCACC[A/G]GCCAGACCACTACTC	9972
rs775224494	snp	A/C	5.04936e-05	0.00502436	missense	NUP153	GRCh38.p7	6:17616531	AATTCTCTTACCCCA[A/C]TGTAAATGCTGCTGG	9972
rs775241137	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17681960	CCCTATAATCCCAGC[A/C]CTTTTAGGAGGCTGA	9972
rs775257809	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17636045	ATATTTCATAATGAA[C/G]ATTCTAGGCCGGGCA	9972
rs775258880	snp	A/G	1.65619e-05	0.00287762	intron-variant	NUP153	GRCh38.p7	6:17669358	AAAGTTGAAAAAATA[A/G]CAAAATTAAGATTTT	9972
rs775260165	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17622412	TGAGGCAGTAGTGAG[C/T]CGAGATTCCACCACT	9972
rs775294839	snp	C/G	6.6246e-05	0.00575488	missense	NUP153	GRCh38.p7	6:17625813	GTAAATGTACCTGCA[C/G]AGCTAGATGTGGTTG	9972
rs775299594	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622334	GGGTGTAGTGGTGGT[A/G]TCTGCCTGTAGTCCC	9972
rs775314165	snp	C/T	3.2962e-05	0.00405954	synonymous-codon, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632780	GAACTTTTCCAATCC[C/T]AGAGAGCCTCCAGAA	9972
rs775379727	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17629910	AAAATTACAAATGCA[C/T]ATACCCTTTGACCTT	9972
rs775380403	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702249	GAGGTAGCTCATGCC[C/T]GTAATACCAGCACTT	9972
rs775388361	snp	G/T	3.2956e-05	0.00405918	missense	NUP153	GRCh38.p7	6:17688422	CTGACTGCTGGCTCA[G/T]GTGTGATTCTCCCAT	9972
rs775413506	snp	C/T			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17707705	GTAAGTGAGCTAGAC[C/T]CAAAGACTGAATCCA	9972
rs775447912	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17669240	TGCACCACCACACCC[A/G]GCTAATTTTTGTATG	9972
rs775451650	snp	A/G	2.53476e-05	0.00355994	intron-variant	NUP153	GRCh38.p7	6:17624844	GGATCCTGGAGGCCC[A/G]AAGAAACACTTAAGT	9972
rs775456549	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694894	TGAGGTAGGAGAATC[A/G]CTTGAACCCAGGACG	9972
rs775481136	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658685	AAGCTCAATAAGTGG[A/G]TGTCTCACAAGCTGA	9972
rs775483035	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17667058	CTTTTATGGATACGA[C/T]ACTCAACCATTAGTA	9972
rs775509500	snp	A/G	4.94197e-05	0.00497066	synonymous-codon	NUP153	GRCh38.p7	6:17637286	ACCAGTGGTTACAGT[A/G]CAGCTGGAAGATGAA	9972
rs775537312	snp	C/G	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637368	TTCACACAAGTTCCA[C/G]GTTTCGGTGTTTCAC	9972
rs775545186	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17666343	CCAACATGGTGAAAA[C/T]GTCTCTACTAAAAAT	9972
rs775576435	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697002	CTTGAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG	9972
rs775621293	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694614	GTGAGCCAAGATCGC[A/G]CCATTGCACTCCAGC	9972
rs775625181	snp	C/G	1.67455e-05	0.00289352	intron-variant	NUP153	GRCh38.p7	6:17647951	AAAAAGAGCTTTTTA[C/G]AAAAATAAAGTGACA	9972
rs775645149	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672175	CTACCGGGAAGCCTA[C/T]GGCAATCAAGACAGT	9972
rs775696215	snp	C/T	1.65045e-05	0.00287263	missense	NUP153	GRCh38.p7	6:17674921	TGATAAGGTGTATTT[C/T]GTAGTTTAGACTGTC	9972
rs775705328	snp	C/T			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615368	AAAAAATCTCTAACA[C/T]AAAATTCAAATTTCA	9972
rs775723724	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17678172	ACCAGACTGGCCAAC[A/G]CGGCAAAATCCCATC	9972
rs775777735	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17627498	TGGTGTTTTTTTGTT[A/G]TTGTTGGGTTTTCTT	9972
rs775804643	in-del	-/CTCCTCCGG	5.15433e-05	0.00507632	cds-indel, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706366	CACCGCCCCCTCCGA[-/CTCCTCCGG]CTCCCGAGGCCATGG	9972
rs775829088	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17626613	CCTTTGTGCACTAAT[C/T]TGCAATGCTGTCTTT	9972
rs775848444	snp	A/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705914	AACCACATCTTTTCC[A/T]TTCTCCCTCGAGAGA	9972
rs775854376	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17634577	AAGTAGCTGGGATTA[C/T]GGGCATCCACGACCA	9972
rs775857811	snp	G/T	1.64751e-05	0.00287007	synonymous-codon	NUP153	GRCh38.p7	6:17647828	TGGAGGTAGTACATT[G/T]GCCTCAGTAGATTTT	9972
rs775879797	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17639097	TTCTTTTTTTTTTAA[A/C]GACAGAGTCTTGCTC	9972
rs775917723	snp	C/T	1.75336e-05	0.00296082	intron-variant	NUP153	GRCh38.p7	6:17665429	TTATTTTCATATAAA[C/T]CAATGATTCATATCT	9972
rs775939594	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17656549	CTGGTTAATTTTTGT[A/T]ATTTTTTTGTACACG	9972
rs775977668	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17690312	AGCCGAATGTGCAGT[A/G]AAATAATTGCTTGAG	9972
rs775990436	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673262	TAATCCCAGCTACTC[A/G]GGAGGCTGACGCAGA	9972
rs775991735	snp	C/T	1.65051e-05	0.00287267	missense	NUP153	GRCh38.p7	6:17688399	CATTTTACTTACCTT[C/T]TGTATTACTGACTGC	9972
rs775994274	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684996	ACATAATTTAAAAGT[C/T]TGAAATACTGCAAGA	9972
rs776022953	snp	C/G	8.2958e-05	0.00643988	intron-variant	NUP153	GRCh38.p7	6:17688624	TAAGAATGCCCTGTT[C/G]AGAGAAAAAACATAT	9972
rs776027271	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17654032	TGGACAGGTAAATTT[C/T]TCTTTTTTGATAAAG	9972
rs776029644	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17686538	GTAGCTGGGACTACA[-/G]GCATGTGCCACCATG	9972
rs776032884	snp	C/G	6.74161e-05	0.00580547	intron-variant	NUP153	GRCh38.p7	6:17649140	GAACAAATGTCACCT[C/G]TATTTATATAATGGT	9972
rs776045499	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17674141	ACAGAGAAAGAAAAC[A/C]GATCCGTGGTTGCCA	9972
rs776065896	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17628619	AACTTGTAAAAAAAA[A/T]AATAATAATAATAAT	9972
rs776081148	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644771	AAACGTGGTGAAACA[C/T]CTCTCTACTAAAAAT	9972
rs776094889	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17700974	CCTGTAATCCCAGCA[C/G]TTCGCGGGAGGCCAA	9972
rs776099676	in-del	-/AAAA			intron-variant	NUP153	GRCh38.p7	6:17644052	CTGTGTTAGCCAATT[-/AAAA]AAAAAAGATAAGGTT	9972
rs776104549	snp	A/T	3.41822e-05	0.004134	missense	NUP153	GRCh38.p7	6:17629522	CTGAGTTCGAAGATG[A/T]GGAAGATGTGTCAAA	9972
rs776113797	snp	A/G	3.29571e-05	0.00405924	missense	NUP153	GRCh38.p7	6:17675686	GCAGGGGATTCCAAC[A/G]TGGAAAAATTCAGAT	9972
rs776156016	snp	A/G	9.93394e-05	0.00704697	synonymous-codon	NUP153	GRCh38.p7	6:17626106	AGAAGTGGCTGGTGT[A/G]CTTGAACTAGAGGAA	9972
rs776189492	snp	C/G	9.568e-05	0.00691599	intron-variant	NUP153	GRCh38.p7	6:17628650	AATAAAAAGTTAATA[C/G]TTACCAGCTGTAGTA	9972
rs776198365	snp	C/T	3.3976e-05	0.00412151	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632635	TCACCTTTATTTTTA[C/T]TTTTTTGGCCTTACC	9972
rs776198387	snp	C/T	1.64942e-05	0.00287173	synonymous-codon, intron-variant	NUP153	GRCh38.p7	6:17639970	ATCTAGAACACTTCC[C/T]TCTTTCAGGATTTCT	9972
rs776218630	in-del	-/GG	3.80532e-05	0.00436178	intron-variant	NUP153	GRCh38.p7	6:17632849	ACTGAACTTCCTAAA[-/GG]AAAAAAAAAAAAAAC	9972
rs776232652	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17691099	GTGAGCTAAGATCAC[A/G]CCATTGCACTCCAGC	9972
rs776270764	snp	A/C	7.13229e-05	0.00597129	intron-variant	NUP153	GRCh38.p7	6:17669044	CTGAAAAAAAAAAAA[A/C]ACACTATTAGAATAG	9972
rs776286933	snp	C/T	1.66679e-05	0.00288681	intron-variant	NUP153	GRCh38.p7	6:17661799	CAAATAAAAAGAAAA[C/T]TAAAACAACTGATAT	9972
rs776287150	snp	A/G	4.97055e-05	0.00498501	intron-variant	NUP153	GRCh38.p7	6:17669343	TTTTTGCATCCTGTT[A/G]AAGTTGAAAAAATAA	9972
rs776294850	in-del	-/TC			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615359	CAAACAACAAAAAAA[-/TC]TCTAACACAAAATTC	9972
rs776377926	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692082	TCTGGAAGGCAAGTA[C/T]AGAACAACTTTAAAT	9972
rs776378779	in-del	-/T	0.000161695	0.00899006	intron-variant	NUP153	GRCh38.p7	6:17628644	AATAATAATAAAAAG[-/T]TAATACTTACCAGCT	9972
rs776389532	snp	A/C	1.66319e-05	0.00288369	intron-variant	NUP153	GRCh38.p7	6:17675811	GAATATACAACTTAG[A/C]GCGATACACTACCAC	9972
rs776396529	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17634390	AACTATGGATTAATG[A/G]CCCCAAATCCGTATC	9972
rs776405572	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17699807	AGCATGGCACTCCAG[C/T]CTGGGTGACAGAGCT	9972
rs776449510	snp	A/C	5.20061e-05	0.00509906	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632622	AGGCGCTTTACCATC[A/C]CCTTTATTTTTATTT	9972
rs776481064	snp	C/G	6.60797e-05	0.00574765	missense	NUP153	GRCh38.p7	6:17674912	GAACCTACCTGATAA[C/G]GTGTATTTCGTAGTT	9972
rs776567220	snp	A/C/G	0.0001165	0.00763142	missense	NUP153	GRCh38.p7	6:17637170	GGTTTCTCAGACATA[A/C/G]AGGACACACACTTAT	9972
rs776568959	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17640616	TATGCAGCCACAGAA[A/C]TCATTCTTTTTCAAA	9972
rs776593798	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17653863	AATGGCACACCTAAG[-/A]ATTTAACATTTCACT	9972
rs776598017	snp	A/G			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17705787	ACTTTCCATGTAACA[A/G]CGCCCCCCACAACTC	9972
rs776615359	in-del	-/TG			intron-variant	NUP153	GRCh38.p7	6:17697295	ATTAAAAATTCAATC[-/TG]GGGATTAGAATTCAA	9972
rs776637790	snp	A/G/T	9.16424e-05	0.00676863	missense	NUP153	GRCh38.p7	6:17624807	CAGATGGTGCTGAGG[A/G/T]TCCAGTTCCAAATAC	9972
rs776659134	snp	A/C	1.84773e-05	0.00303946	missense	NUP153	GRCh38.p7	6:17646153	CTAAATGTAAATCCA[A/C]TCTGTAAAGAGAAAG	9972
rs776659435	snp	C/G	1.64762e-05	0.00287016	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632765	TCCCTCGGGTTTCTT[C/G]AACTTTTCCAATCCT	9972
rs776682589	snp	C/T	1.648e-05	0.0028705	synonymous-codon	NUP153	GRCh38.p7	6:17661662	CCCTACCTCCTCCTC[C/T]AGAGGTTTAGAAGCA	9972
rs776725523	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17638148	TCATCCATTTCTTCT[C/T]TTAAGTGTTCCATTG	9972
rs776732599	in-del	-/TAT	3.34992e-05	0.00409249	intron-variant	NUP153	GRCh38.p7	6:17688637	TTGAGAGAAAAAACA[-/TAT]TATGACAGTTTTAGA	9972
rs776736615	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17664808	CTGTAATCCCAGCAC[G/T]TTGGGAGGCCAAGGC	9972
rs776768538	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	NUP153	GRCh38.p7	6:17647807	TTGCTTGTTACTTAC[A/G]GATGATGGAGGTAGT	9972
rs776782217	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17698962	CTTTTTCTCAGGTAA[-/C]CATGTTTGAAAATTG	9972
rs776785587	snp	C/T	6.81814e-05	0.00583833	intron-variant	NUP153	GRCh38.p7	6:17665413	GAGAAATCAAAAACA[C/T]TTATTTTCATATAAA	9972
rs776807350	snp	C/T	4.99322e-05	0.00499636	intron-variant	NUP153	GRCh38.p7	6:17669569	GTAAACCCTATATTA[C/T]TTGTTGCAACATAAA	9972
rs776821972	snp	C/G	1.6473e-05	0.00286988	missense	NUP153	GRCh38.p7	6:17637264	ATTTATCTCCAAATC[C/G]TAAGGTACCAGTGGT	9972
rs776848348	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693006	CTAAAGTGAATCAGG[C/T]AAACAAATCTTACAG	9972
rs776858845	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17687977	AAAAAAAATTAGCTA[A/G]GTGTGGTGGCAGGCG	9972
rs776868910	in-del	-/GCTCC			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704841	CTCTGCTCACGGCAA[-/GCTCC]GCCTCCCGGGTTCAA	9972
rs776871538	in-del	-/CTT	2.05912e-05	0.00320861	intron-variant	NUP153	GRCh38.p7	6:17669081	AGTTATGAAAAATAC[-/CTT]TTTTTTTTTTTTTGA	9972
rs776885237	snp	A/G	1.75483e-05	0.00296207	intron-variant, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706251	TTCCCCACCCGCCAG[A/G]CCACCGCGGCGTCGG	9972
rs776900893	snp	A/G	1.70481e-05	0.00291955	missense	NUP153	GRCh38.p7	6:17629516	AGGCTGCTGAGTTCG[A/G]AGATGAGGAAGATGT	9972
rs776908316	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17618567	TAAAATCTCTCTTTT[-/TT]TTTTTTTTTTTTTTA	9972
rs776918941	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17685103	ACAAACTCAATTTGT[-/A]AAAAAATGCAGTATG	9972
rs776920537	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619551	CTTACTTCAGCAGCA[C/T]ATACCCAAAACTTGA	9972
rs776958529	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17648050	TCACTTTAAATTCTG[A/G]AAAACACAGAACTGT	9972
rs776962489	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17654572	TGATCCGCCCACCTC[A/G]GCCTCCGAAAGTGCT	9972
rs776969753	snp	A/G	1.72692e-05	0.00293842	intron-variant	NUP153	GRCh38.p7	6:17665217	AATATTCAAAGACTG[A/G]TAGAAATATACATAT	9972
rs776984358	snp	A/C	1.64808e-05	0.00287057	missense	NUP153	GRCh38.p7	6:17665315	GGTTTAAAATAAACA[A/C]TTCGATTTGTTGCTA	9972
rs777009827	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648844	TAAAAGATGTTACGC[C/T]TAGCTGAGAAGTAAA	9972
rs777015263	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642950	TATGATTCTACTTAC[A/G]TGACATATTCAGAAT	9972
rs777043203	snp	C/T	1.65004e-05	0.00287227	missense	NUP153	GRCh38.p7	6:17629419	AATCCTCCCTGATCT[C/T]CAAATTTAAAATTTC	9972
rs777090044	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17672052	TCCTAGCAGACTGTA[G/T]AAACAAGCCAATTTT	9972
rs777090317	snp	C/G			downstream-variant-500B	NUP153	GRCh38.p7	6:17614899	ATTCAGATACTTTCA[C/G]ATACTTTCCCTTTCT	9972
rs777118468	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643826	TATAATGAAACAAAG[C/T]TGTTGTAACAAATTG	9972
rs777126395	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695229	TATCTAGTCACTTAT[A/G]AAAGGACTAAAACAG	9972
rs777146423	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17695969	AGCTGAGATTGCACC[A/T]CTGCACTCCAGCCTG	9972
rs777162296	snp	C/T	1.66324e-05	0.00288374	missense	NUP153	GRCh38.p7	6:17675368	TTTGAAACAGTTATA[C/T]CTGAAACAAAATTAC	9972
rs777175701	snp	A/C	1.67494e-05	0.00289386	intron-variant	NUP153	GRCh38.p7	6:17624540	CCCATACAGATACTA[A/C]CAGCATCACAGCACA	9972
rs777179366	snp	C/G/T			intron-variant	NUP153	GRCh38.p7	6:17684236	TTATAGAATGCAAAA[C/G/T]GGACTAATAAACCAC	9972
rs777186570	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17628544	CTGTATTTCTCAACT[A/G]TGTTCAGTGTAAACC	9972
rs777201508	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17684714	AACTTACATACTTAC[A/T]GCTTTTGGATAAAAG	9972
rs777214308	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17694525	CAGCTGGGCATGATG[A/G]TGATGCCTGTAATCC	9972
rs777219143	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17653078	GGCAACATGGTGAAA[-/C]CCTGTCTCTAATGAA	9972
rs777236935	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708497	ACAGGCATGTGCCAC[A/G]ACGGCCGGCTAATTT	9972
rs777246335	snp	C/T	3.29587e-05	0.00405934	missense	NUP153	GRCh38.p7	6:17674991	GATAAAAAGGAGAAT[C/T]TCCAAGCTGACTGGT	9972
rs777276681	in-del	-/TTACCATATATAGCTATAT			intron-variant	NUP153	GRCh38.p7	6:17620258	TACACAAAGCTATAC[-/TTACCATATATAGCTATAT]GAGACTGGTATAAAA	9972
rs777283526	in-del	-/TTTG	0.0330485	0.124226	intron-variant	NUP153	GRCh38.p7	6:17616745	AAAATGATAGGTTTT[-/TTTG]TTTGTTTGTTTGTTT	9972
rs777291509	snp	C/T	1.71493e-05	0.0029282	missense	NUP153	GRCh38.p7	6:17624792	CAAATGCTGGACTGG[C/T]AGATGGTGCTGAGGG	9972
rs777311171	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17617655	TGAGAACAACCTAGG[C/T]AACATGGCGAGATCC	9972
rs777329055	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17683976	TGAATGGCTTGGTAC[C/T]CTACCCAAGGTAGTG	9972
rs777350821	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17644527	TCTCTTGTTCCTGTG[C/T]CCTTGAGCTTTGTGT	9972
rs777360572	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627956	GATATTTCCCCAAAA[C/T]TTCTTATCTTCTAGG	9972
rs777391894	in-del	-/AAAGGCTTATCTTT	1.68185e-05	0.00289982	intron-variant	NUP153	GRCh38.p7	6:17639913	ATGAGTTTGTAATCA[-/AAAGGCTTATCTTT]TAATTATCTTACCAG	9972
rs777403331	snp	A/G	5.13237e-05	0.00506549	intron-variant	NUP153	GRCh38.p7	6:17625782	GTCCATCCAATTACA[A/G]TGCATTTTTTCTTTT	9972
rs777423583	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17695047	GGTGCTAAGACCCAA[A/G]TACAGGCGTGTCCTT	9972
rs777435055	snp	C/T	0.000100381	0.00708383	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706292	CTGATGCTGTTGTCG[C/T]CCCTGCTGGTAAGGC	9972
rs777488757	snp	C/G/T	8.24578e-05	0.00642051	missense	NUP153	GRCh38.p7	6:17616177	ACACATTTTTCCCAT[C/G/T]TGACCTGTGAAAAAT	9972
rs777501169	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700765	AGACCTTGGTCTTTT[C/T]TCATACAAGCTAAGA	9972
rs777503498	snp	C/T	1.64906e-05	0.00287142	intron-variant	NUP153	GRCh38.p7	6:17647790	TAAATATATACTATT[C/T]CTTGCTTGTTACTTA	9972
rs777516463	snp	A/T	3.29968e-05	0.00406169	synonymous-codon	NUP153	GRCh38.p7	6:17629148	AAAACCTGCAGAGGA[A/T]GATTTGGGCAGTTCC	9972
rs777553848	snp	A/G	6.97666e-05	0.0059058	intron-variant	NUP153	GRCh38.p7	6:17674868	AGTGTAAAAAAAAAG[A/G]AAAAAAAAGATCATC	9972
rs777575823	snp	C/T	0.000116151	0.00761984	missense	NUP153	GRCh38.p7	6:17629261	GTCCAAACTTAAAAT[C/T]ATCATTCTTACTATC	9972
rs777608058	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17702172	AAGACAGGAACTAAC[C/T]ACATTCTCTTCAGTT	9972
rs777609001	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17662798	CTCAACGGTCTTCAC[C/T]GCCAAAAGTAGGTAA	9972
rs777610138	snp	C/G	1.64819e-05	0.00287066	synonymous-codon	NUP153	GRCh38.p7	6:17647894	AGTGCTGCTCGGAGA[C/G]GTCATTTGTACCTGG	9972
rs777616516	in-del	-/TTGGGAGGCCGAGGCGGGTGGATCACGAAG			intron-variant	NUP153	GRCh38.p7	6:17631723	TGTAATCCCAGCACT[lengthTooLong]TCAGGAGATTGAGAC	9972
rs777655626	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17688835	ATAAGGCAATAATTG[C/T]CCCAAATGGCTGCAT	9972
rs777730145	snp	A/T	3.37075e-05	0.00410519	intron-variant	NUP153	GRCh38.p7	6:17665403	TACAGGTAAAGAGAA[A/T]TCAAAAACATTTATT	9972
rs777749542	snp	A/T	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637344	ACCACTGTCAATGTA[A/T]GGGCTCGCTTCACAC	9972
rs777772849	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17681701	ATTTATCTGCAATCA[C/G]GATTTACATACACAT	9972
rs777777668	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17674598	AACACAGTGAAACCC[A/G]TCTCTACTAAAAATA	9972
rs777783532	snp	C/T	3.84667e-05	0.00438542	intron-variant	NUP153	GRCh38.p7	6:17629581	AGACACTCAATGTAC[C/T]GATCCTCTCAAACAA	9972
rs777804680	in-del	-/ACCACA	8.33035e-05	0.00645328	intron-variant	NUP153	GRCh38.p7	6:17675822	TTAGAGCGATACACT[-/ACCACA]AATGGTTTTTACTTT	9972
rs777820201	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17682438	CGACTGACTATTCCT[G/T]TAACGAAAGATTTCT	9972
rs777874849	snp	A/C/T			intron-variant	NUP153	GRCh38.p7	6:17687930	CCATCCTGGCTAACA[A/C/T]GGTGAAACCCCGTCT	9972
rs777899798	snp	C/T	4.95152e-05	0.00497545	missense	NUP153	GRCh38.p7	6:17626076	GGTGGAACTACCAAA[C/T]ATGCCACCACCAGCA	9972
rs777952400	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699367	CAGGAATAATGGTGC[A/G]TGCTACTCCAGAGGC	9972
rs778026319	snp	G/T	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17624623	TGTCCAAACACAGGG[G/T]GCTGGCTACTGCTTG	9972
rs778050059	in-del	-/TTTT	6.74093e-05	0.00580518	intron-variant	NUP153	GRCh38.p7	6:17616742	GGGCAAAATGATAGG[-/TTTT]TTTGTTTGTTTGTTT	9972
rs778060420	snp	A/G	1.69055e-05	0.00290731	intron-variant	NUP153	GRCh38.p7	6:17624523	TTTTAAGACACACAA[A/G]ACCCATACAGATACT	9972
rs778067202	snp	C/G	1.69063e-05	0.00290738	missense	NUP153	GRCh38.p7	6:17629511	TGAGGAGGCTGCTGA[C/G]TTCGAAGATGAGGAA	9972
rs778134473	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17694189	CACTGCTGTATCCTC[C/T]GTATTTAATGCTTGA	9972
rs778141719	snp	C/T	2.00809e-05	0.00316861	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706474	GAGCCTCCCCCGCCG[C/T]CCGGCCCCGGCCCAA	9972
rs778152160	snp	A/G	8.23879e-05	0.00641772	missense	NUP153	GRCh38.p7	6:17628948	GGCTCCACGTTGCCA[A/G]AAGAGAATCCTCCTT	9972
rs778153391	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17671329	TCATAAAAGGTACTG[G/T]GAAGTGTTCCCTACT	9972
rs778166272	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17679313	GAATAAAATATTTAG[G/T]AATGAACCAAGGTAA	9972
rs778172628	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17649888	GTATGACCTGGGATT[C/G]TTGGAACATATCCCT	9972
rs778207268	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17689137	ATGCCTGTAATCCTA[A/G]CACTTTGGGGGACTG	9972
rs778253520	snp	C/G/T	4.9482e-05	0.00497383	missense, synonymous-codon	NUP153	GRCh38.p7	6:17669514	AGATTGTGCACTGAG[C/G/T]TGCTTAGCTTTCATT	9972
rs778268934	snp	A/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17706887	GCCGTTGCGCCTATT[A/G]CCCCTGCTAAGGCGG	9972
rs778277854	snp	A/G	9.98419e-05	0.00706477	intron-variant	NUP153	GRCh38.p7	6:17649308	TCCATTTCCTAAAAC[A/G]TAACATGTTGCATGA	9972
rs778326084	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17694971	GCAACAAAGCGAGAC[G/T]CTGTCTCAAGGAAAA	9972
rs778336501	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627119	ATCCAGGGCTGGTCA[C/T]AGTACACTATGGGCA	9972
rs778339576	snp	A/G	1.65751e-05	0.00287876	intron-variant	NUP153	GRCh38.p7	6:17661627	TTTTAAATAAACCTC[A/G]AGAGTATATGAGTAT	9972
rs778360376	snp	A/G	1.70124e-05	0.00291649	intron-variant	NUP153	GRCh38.p7	6:17674860	CCAGTTAAAGTGTAA[A/G]AAAAAAGAAAAAAAA	9972
rs778376089	snp	A/T	1.64882e-05	0.00287121	synonymous-codon	NUP153	GRCh38.p7	6:17669436	AAAATTTACCGCTAA[A/T]GGGCTTGACATCTTC	9972
rs778385534	snp	A/C	4.94238e-05	0.00497086	missense	NUP153	GRCh38.p7	6:17637233	GAACACTCCCAAGAT[A/C]CAATGGGCCTTTTGA	9972
rs778400808	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17660159	TCCAAACCTGCAGAG[C/G]AAAATACCAATAGGC	9972
rs778460324	snp	A/G	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17624671	GGTGGTGCAGGCTGA[A/G]AACCAGTGGGAAATA	9972
rs778507563	in-del	-/TTGT			intron-variant	NUP153	GRCh38.p7	6:17703413	GCGCCAGACCTCTCA[-/TTGT]TTCTTACTCCAACTT	9972
rs778551595	snp	A/G	3.29755e-05	0.00406038	synonymous-codon	NUP153	GRCh38.p7	6:17629127	AATAACACCTGTACC[A/G]AAGCTAAAACCTGCA	9972
rs778588268	snp	A/G	5.52746e-05	0.00525683	intron-variant	NUP153	GRCh38.p7	6:17626209	AAATCCTTAAGAATA[A/G]TCTCAGAAAGTACTT	9972
rs778592120	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17677312	CCAACACTCTTCAGA[A/G]GAAGATGACAGAACC	9972
rs778595340	in-del	-/AAAC			intron-variant	NUP153	GRCh38.p7	6:17656211	CTCTGACAAATAAAT[-/AAAC]AAACAAACCACAAGG	9972
rs778601301	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672807	AACGTAGTAAGACTC[C/T]TACCTTTCATTTTTT	9972
rs778628658	snp	A/C	1.67186e-05	0.0028912	synonymous-codon	NUP153	GRCh38.p7	6:17626142	GTTCAAGAAACTAAA[A/C]ACTGGCTTTGCTGCA	9972
rs778672478	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17664273	TTTACCATTATGATG[C/G]CTTAACAGTTGAACA	9972
rs778683381	snp	C/G/T	3.29578e-05	0.00405931	missense	NUP153	GRCh38.p7	6:17688584	CACCCTGGCACAATA[C/G/T]TCTTAACAGATTCTG	9972
rs778683985	snp	C/G			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632359	CAAAGAACAGTTCAC[C/G]TAGGGGGCTAGCAGT	9972
rs778692347	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17651004	TAAATAGTGCAAAAG[A/G]GGGAGAGTTAAAAAT	9972
rs778740553	snp	C/T					GRCh38.p7	6:17673486	CTCAAAATTTATTAA[C/T]AAGAAAATAACCCAA	9972
rs778771177	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17683656	CATAATTCTTAGGAG[C/G]CCTAGGATCTTTGAT	9972
rs778822567	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17648260	GGAAGCCATGACAGA[C/G]GGAATTGCTTGAACG	9972
rs778823890	snp	A/G	3.30431e-05	0.00406454	synonymous-codon	NUP153	GRCh38.p7	6:17665380	AGGAGGATATTGAGA[A/G]TCCACCTTACAGGTA	9972
rs778842384	snp	A/G	0.000105417	0.00725929	missense	NUP153	GRCh38.p7	6:17646120	CCAGAAAGTTCTGCT[A/G]TTTTTGCAACAGGCA	9972
rs778844129	in-del	-/AACATGGAA	3.29571e-05	0.00405924	cds-indel	NUP153	GRCh38.p7	6:17675683	AATGCAGGGGATTCC[-/AACATGGAA]AAATTCAGATGGCTC	9972
rs778864149	snp	C/T	0.000148296	0.00860964	synonymous-codon	NUP153	GRCh38.p7	6:17675640	ACTGCCAATTGGGAA[C/T]GCCGAGGATGTAGAT	9972
rs778865863	snp	A/C	1.65853e-05	0.00287964	intron-variant	NUP153	GRCh38.p7	6:17675509	ATTATGTACTACCAC[A/C]TGTCAAGAATACCTT	9972
rs778897339	snp	A/G	1.65086e-05	0.00287298	intron-variant	NUP153	GRCh38.p7	6:17647778	CTTTGAAATCAGTAA[A/G]TATATACTATTCCTT	9972
rs778911041	snp	A/G	3.2993e-05	0.00406145	synonymous-codon	NUP153	GRCh38.p7	6:17626052	AGCCACAGGTGGATT[A/G]GAGGAAGAGGTGGAA	9972
rs778948727	snp	A/G	1.64871e-05	0.00287111	missense	NUP153	GRCh38.p7	6:17665286	TCCTGAATTCACCAG[A/G]AGGAGTCAGAGATGG	9972
rs778950995	in-del	-/TGT	1.64787e-05	0.00287038	cds-indel	NUP153	GRCh38.p7	6:17616642	ACACTCCTGATGGAC[-/TGT]TGTTTGTGAAGTTGA	9972
rs778990955	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642006	TTTTTCTTTTTAAGT[A/G]TTTGCCAATTTAAAA	9972
rs778994166	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697208	GCTAAATCCACTGGG[C/T]ATTCTCTCTCCAAGA	9972
rs779007110	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17621789	GAGAGCACAGTAGAG[A/T]TAACAATAATTTATT	9972
rs779010668	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668518	TTGTCCTGAGGACTG[C/T]AGAAGAGAGTAAAAT	9972
rs779014796	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17623211	TCCAATTTCATATTA[A/G]AGGAAAAAATCCTGA	9972
rs779059675	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17679071	GATAAAAACACTCAA[C/T]AAACTAAGACTAGAA	9972
rs779121825	snp	C/G	1.65111e-05	0.0028732	missense	NUP153	GRCh38.p7	6:17649285	AGATTTTCGGTAATA[C/G]TGGAACTTCCATTTC	9972
rs779138222	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17687451	AAAGCAATCTTGAAA[A/C]GTACAGACATTAAAA	9972
rs779144465	snp	A/T	1.66175e-05	0.00288244	synonymous-codon	NUP153	GRCh38.p7	6:17669302	ACTTACAGAATTCAG[A/T]GGAGAAGAAACAATG	9972
rs779163456	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681283	CAGTGGGCAACTCAT[A/G]GAGACAGAGAATAGA	9972
rs779164520	snp	C/T	1.64789e-05	0.0028704	synonymous-codon	NUP153	GRCh38.p7	6:17649199	CGAATTGATGGGTGA[C/T]GGAGAGGAAGTTGTG	9972
rs779193708	snp	C/G			missense	NUP153	GRCh38.p7	6:17629539	GAAGATGTGTCAAAG[C/G]CTACAAAAATATAAA	9972
rs779197465	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676588	AAAGAGGCTTCCAGT[C/T]AGAACGGAATAAGTG	9972
rs779209663	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	NUP153	GRCh38.p7	6:17628853	TCTTCCCAAAAACTA[A/G]GGAAGTAGAAGTGAC	9972
rs779224537	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17692660	ACCCTAAGTCATTAA[A/G]AAAAAGTTAAATTAA	9972
rs779232489	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17680277	ATACAGACCATGGAC[A/G]TGAACACAGGGCCCA	9972
rs779243306	snp	A/C	1.98002e-05	0.00314638	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706399	CCATGGCGGAGCCTC[A/C]GCCGCTTCCCGCTCC	9972
rs779251127	snp	A/C	1.6477e-05	0.00287024	missense	NUP153	GRCh38.p7	6:17616636	ATGTGAACACTCCTG[A/C]TGGACTGTTGTTTGT	9972
rs779285993	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17681653	GGTATAGGTATTTAA[A/G]CCAATTAGCATTTAC	9972
rs779301405	snp	G/T	3.36151e-05	0.00409957	missense, utr-variant-3-prime, intron-variant	NUP153	GRCh38.p7	6:17632833	TGCTACTTGAAGCAG[G/T]TACTGAACTTCCTAA	9972
rs779304345	snp	G/T	1.68451e-05	0.00290211	intron-variant	NUP153	GRCh38.p7	6:17616742	GGGCAAAATGATAGG[G/T]TTTTTTGTTTGTTTG	9972
rs779329844	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17698001	TTGACTTCAGTTCTG[C/T]TCAACTCCCTTTTCT	9972
rs779351674	snp	A/T	1.65015e-05	0.00287237	intron-variant	NUP153	GRCh38.p7	6:17669424	ATCGTGATTTTAAAA[A/T]TTTACCGCTAAAGGG	9972
rs779417315	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17647502	AAATTTCTTGGGTAT[A/G]ATAGCTGTATTGTGG	9972
rs779434708	snp	C/G	1.64738e-05	0.00286995	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632739	ACTAGGCACAATTCA[C/G]AGTCCCAGCTTCCCT	9972
rs779442568	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17658476	GTTTGCAAAGGAGAC[A/G]AGAGCCTTGAAGATG	9972
rs779470024	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17691703	GTGGGAGGCAGACGG[A/G]CCATTGCACTCCAGC	9972
rs779517804	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17619267	CTTACCAAACATGGG[A/G]AGAGAATAAAGATCC	9972
rs779534014	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17691149	GAGACTCCGTCTCAA[-/G]GAAAAAAAAAGGAAA	9972
rs779535386	snp	A/G	1.76456e-05	0.00297026	missense	NUP153	GRCh38.p7	6:17646108	GTACTACTAGAACCA[A/G]AAAGTTCTGCTGTTT	9972
rs779573552	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636771	TACCCCCTAAAGAAA[C/T]CTTCCCTGTAAATGA	9972
rs779590384	snp	A/G	1.76839e-05	0.00297349	intron-variant	NUP153	GRCh38.p7	6:17637122	CAACAGAAGTAATAA[A/G]CAAAATTACTCCATA	9972
rs779607022	snp	C/G/T	3.29545e-05	0.00405911	missense	NUP153	GRCh38.p7	6:17628964	AAGAGAATCCTCCTT[C/G/T]GGTGGCAGGCATTTC	9972
rs779608562	in-del	-/A	0.000354123	0.0133017	intron-variant	NUP153	GRCh38.p7	6:17674868	AGTGTAAAAAAAAAG[-/A]AAAAAAAAGATCATC	9972
rs779615745	snp	C/T	1.70977e-05	0.00292379	intron-variant	NUP153	GRCh38.p7	6:17688370	AAAACCTATCATTCA[C/T]GACAAAATATTCACA	9972
rs779649941	snp	C/T			intron-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17704239	GGAGCTTGCAGTGAG[C/T]CAAGATCGCGCCACT	9972
rs779660720	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17647095	AGTATGACACTTCTG[A/G]GGCAACTGATGGATT	9972
rs779662573	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17650399	TACATATAAGCCACC[C/T]GAATCTCTGGTGGAC	9972
rs779707065	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17687225	ATAGAAAAGATCATT[C/T]CTACAGCTATCTTAG	9972
rs779725005	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17636579	ACAAAACCATCATCC[A/C]CTTCTGGATGAGTTA	9972
rs779725124	in-del	-/CTT			intron-variant	NUP153	GRCh38.p7	6:17648940	ATTTACAAGAATATC[-/CTT]CTCTATGGTATTGCA	9972
rs779736639	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17693931	AGTAGAAATTTGCAT[A/G]GCCTCTTTACTTTTT	9972
rs779774082	snp	A/G	4.19472e-05	0.0045795	intron-variant	NUP153	GRCh38.p7	6:17646185	ATATCCTTATACTTC[A/G]TTTTCAATAAGTATC	9972
rs779809314	snp	A/G	1.66018e-05	0.00288108	missense	NUP153	GRCh38.p7	6:17629300	CTTCTTCGGGCTTAG[A/G]TTCAGATGAAACTCC	9972
rs779829773	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17653972	GGGGTGAAGTGTACT[A/G]ATGTCTTCAACTATC	9972
rs779833512	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17643472	ATGTGCAACACCCAC[C/T]CCCAACCATCCCCAC	9972
rs779858702	snp	C/G/T	1.64933e-05	0.00287165	missense	NUP153	GRCh38.p7	6:17626051	TAGCCACAGGTGGAT[C/G/T]GGAGGAAGAGGTGGA	9972
rs779859475	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17676545	GAGGCATTTTCAAAA[A/G]CTTTAGAATTGTTTC	9972
rs779866201	snp	A/T	1.64844e-05	0.00287087	intron-variant	NUP153	GRCh38.p7	6:17662109	TTACGTTTGCTTATT[A/T]GTTGTAATTTTCTTA	9972
rs779918632	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17693925	TTCTCTAGTAGAAAT[C/T]TGCATGGCCTCTTTA	9972
rs779924278	snp	C/T	1.64732e-05	0.0028699	missense	NUP153	GRCh38.p7	6:17637567	TGGGTGACAATTTTG[C/T]TGCTTGACAGGCTAT	9972
rs779956202	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17671569	ACAAAATATGTTCGA[C/G]ATCTGTATGCTGAAC	9972
rs779959742	snp	C/T	1.6617e-05	0.00288239	intron-variant	NUP153	GRCh38.p7	6:17675498	TTACTACCCAAATTA[C/T]GTACTACCACATGTC	9972
rs779964589	snp	C/T	6.59163e-05	0.00574054	synonymous-codon	NUP153	GRCh38.p7	6:17625920	TGTACCTGTGCTGGA[C/T]GTGGTTGCTAGTTTG	9972
rs779991166	snp	A/G	2.85351e-05	0.00377714	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706432	GGCGGGTAAGGGGGC[A/G]GGAGAGGCAGAGGCG	9972
rs779992043	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17642338	ATCTGGTAAGGGTCT[A/G]GTGTCCAGACTAAGA	9972
rs779997743	snp	A/G	1.83296e-05	0.00302729	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706388	GGCTCCCGAGGCCAT[A/G]GCGGAGCCTCCGCCG	9972
rs780013319	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17683944	GAAGTCTTTGGGTCA[A/T]GGGGGCAGATTCCTC	9972
rs780046059	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17682626	TAGATTCCATCTCAC[A/G]AAACCACTTTTGCCA	9972
rs780049884	snp	C/T	3.29804e-05	0.00406068	missense	NUP153	GRCh38.p7	6:17665280	TAGTCTTCCTGAATT[C/T]ACCAGAAGGAGTCAG	9972
rs780052229	snp	A/G	3.29995e-05	0.00406185	missense	NUP153	GRCh38.p7	6:17629386	ATAGACCCAGAATCG[A/G]ATGACACACCTATTT	9972
rs780052978	snp	C/G	3.2962e-05	0.00405954	missense	NUP153	GRCh38.p7	6:17616608	GCTGCAGGTGTGCTA[C/G]AATTTGCACCAAATG	9972
rs780097780	snp	A/G	1.64825e-05	0.00287071	missense	NUP153	GRCh38.p7	6:17649185	GTTAATGCTTGAGAC[A/G]AATTGATGGGTGATG	9972
rs780111115	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17661570	GGGTCTCTTCGAACC[C/T]CACCCCTACAGGTCT	9972
rs780115815	in-del	-/C			intron-variant	NUP153	GRCh38.p7	6:17673834	ATACTTACCATATGA[-/C]CCATCAATTCAACTC	9972
rs780116615	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17652625	CAAAAGATATCATTA[A/G]GAAAATGAGTAGGCA	9972
rs780152799	snp	A/T	1.64844e-05	0.00287087	missense	NUP153	GRCh38.p7	6:17649275	ATCGGTAGAGAGATT[A/T]TCGGTAATACTGGAA	9972
rs780165703	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17628550	TTCTCAACTATGTTC[A/G]GTGTAAACCATTAAT	9972
rs780199182	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17682324	ACAGGTCTTTGCCTC[-/A]AATGTTGATGGCTAC	9972
rs780201362	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17622893	CCCAGCACTGTGGGA[A/G]GCCGAGGTGGGTGGA	9972
rs780245920	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17621443	CAACAGCCAAGATAC[A/G]GAATCAATCTAAGTG	9972
rs780262077	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17622098	TGTAGCATGGCTTTT[C/G]TTTTGTTTTGTTTTG	9972
rs780264869	snp	C/T	8.36799e-05	0.00646784	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706320	GGCTTAATTGGCCCC[C/T]GGTGGCAACGCCGCG	9972
rs780265154	snp	A/G	3.30868e-05	0.00406723	missense, intron-variant	NUP153	GRCh38.p7	6:17639950	TTACCAGGGCTTTTC[A/G]GAATATCTAGAACAC	9972
rs780273479	snp	A/G	1.65726e-05	0.00287855	intron-variant	NUP153	GRCh38.p7	6:17675774	TTGTTGAAGGTTCTT[A/G]AAAGAAAAGCATTAA	9972
rs780278240	snp	C/T	1.66546e-05	0.00288566	intron-variant	NUP153	GRCh38.p7	6:17669290	GTTTAAATCTCAACT[C/T]ACAGAATTCAGAGGA	9972
rs780292174	snp	C/G	1.80263e-05	0.00300214	missense, intron-variant	NUP153	GRCh38.p7	6:17669022	CTATCCCACTCCTAT[C/G]AAGAGGCTGAAAAAA	9972
rs780364960	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701943	AAGATAAATGTCTGA[A/G]GCATACTACCCACAC	9972
rs780372970	snp	C/T	1.65389e-05	0.00287562	missense	NUP153	GRCh38.p7	6:17628734	CTCAGATGGTTTTGT[C/T]ATACTAAAACTAAAT	9972
rs780373631	in-del	-/AATAAT			intron-variant	NUP153	GRCh38.p7	6:17628620	ACTTGTAAAAAAAAA[-/AATAAT]AATAATAATAATAAA	9972
rs780389956	snp	A/G	6.59761e-05	0.00574314	intron-variant	NUP153	GRCh38.p7	6:17661987	ACAAGTTAAATATAA[A/G]GAAGTATAGCTGTAT	9972
rs780443103	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17669913	CAGCCTGGGCAACAT[A/G]GTGAAACCCCATCTG	9972
rs780464053	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17619187	AGCCAGAAAAGTCTA[C/T]AATGGAGAAATGCTT	9972
rs780464626	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17658342	CAGAGGCTGCAGTGA[C/G]CTGAGATCATGCTAC	9972
rs780476618	snp	C/G	1.74372e-05	0.00295268	intron-variant	NUP153	GRCh38.p7	6:17688360	TTAGGGCATGAAAAC[C/G]TATCATTCATGACAA	9972
rs780494798	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700647	GGCAGGACATACTTA[C/T]TTGGGACAGAGTATC	9972
rs780506837	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17697818	GGGGTGGGGGAAGGC[C/T]ATTCTATAACACTAA	9972
rs780513695	snp	A/T	1.67351e-05	0.00289263	synonymous-codon	NUP153	GRCh38.p7	6:17624781	CTGGTTAGCACCAAA[A/T]GCTGGACTGGCAGAT	9972
rs780528195	in-del	-/TTTTTT			intron-variant	NUP153	GRCh38.p7	6:17635113	GCTTATCTTTTTTTT[-/TTTTTT]TTTTTTTTTGAGACG	9972
rs780554248	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17696165	CAAAAAAGTTAAGGG[A/G]CCCTGCCTACCAAAC	9972
rs780595900	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17676617	TGGGACCAGACCAGT[C/T]CTTCTACTGTAAACA	9972
rs780596371	in-del	-/AAAC			intron-variant	NUP153	GRCh38.p7	6:17696128	AGTGAAACTGTCTCA[-/AAAC]AAACAAACCAACCAA	9972
rs780602202	snp	C/T	1.64746e-05	0.00287002	missense, downstream-variant-500B, intron-variant	NUP153	GRCh38.p7	6:17632713	ATTTGGTAGAGTCTG[C/T]CTTATTCTGCACTAG	9972
rs780613331	in-del	-/A	0.465133	0.12735	intron-variant	NUP153	GRCh38.p7	6:17632847	GGTACTGAACTTCCT[-/A]AAAAAAAAAAAAAAA	9972
rs780640363	snp	A/G			intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632564	GAATGAGTGAACACT[A/G]AAGCTGTTCTCAAAT	9972
rs780668136	snp	G/T	1.6483e-05	0.00287076	intron-variant	NUP153	GRCh38.p7	6:17662102	CACATATTTACGTTT[G/T]CTTATTTGTTGTAAT	9972
rs780668884	in-del	-/T	1.71882e-05	0.00293152	intron-variant	NUP153	GRCh38.p7	6:17668969	TAAATGCTAAAGAAG[-/T]TTTACCTTTTCTCTT	9972
rs780722372	snp	A/G/T	0.107292	0.205432	intron-variant	NUP153	GRCh38.p7	6:17632847	GGTACTGAACTTCCT[A/G/T]AAAAAAAAAAAAAAA	9972
rs780822410	snp	G/T			intron-variant	NUP153	GRCh38.p7	6:17617756	AGGCTGAGGTGGGAA[G/T]ATCTTCTGAGCCTAG	9972
rs780826693	in-del	-/T	0.000105731	0.00727008	intron-variant	NUP153	GRCh38.p7	6:17646048	TTGTATGTTAAAATG[-/T]TAAGAAATTTTTACT	9972
rs780860400	snp	A/G	1.64765e-05	0.00287019	synonymous-codon	NUP153	GRCh38.p7	6:17675289	TGAGCTGGTGGCAGT[A/G]TGCTGTGAGAGTGAG	9972
rs780901352	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17673924	CTTCATTCATAATTG[A/C]CAGAAACTGGAAACA	9972
rs780912689	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635355	ACCTGGTGATCCACT[C/T]GCCTCGGCCTCCCAA	9972
rs780945616	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17684847	GAGAAAAGAGGGGAA[C/T]AGCCAGTTGGTGGAG	9972
rs780954046	snp	A/C	1.64727e-05	0.00286986	missense	NUP153	GRCh38.p7	6:17637358	AAGGGCTCGCTTCAC[A/C]CAAGTTCCAGGTTTC	9972
rs780956672	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17689203	CCAGCCTGACCAACA[C/T]GGAGAAACCCCATCT	9972
rs780970143	snp	A/T	1.65578e-05	0.00287726	missense	NUP153	GRCh38.p7	6:17629382	GTTTATAGACCCAGA[A/T]TCGGATGACACACCT	9972
rs780972320	snp	C/G	1.69481e-05	0.00291098	intron-variant	NUP153	GRCh38.p7	6:17625793	TACAATGCATTTTTT[C/G]TTTTGTAAATGTACC	9972
rs781038491	snp	C/T	1.65021e-05	0.00287241	missense	NUP153	GRCh38.p7	6:17675024	TAAGGATTGAAGAAT[C/T]CCCAAGTGACTGCAC	9972
rs781038628	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17692895	AACAGATGAATAAAA[C/T]TGTGCATTCTTGAAA	9972
rs781044655	in-del	-/G			intron-variant	NUP153	GRCh38.p7	6:17673131	CCCAGCACTTTGGGA[-/G]GCCAACGCGGGTGAA	9972
rs781086449	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17668422	GGTAACAGTAAGCCA[C/T]AAAGTCTGTCAAGAT	9972
rs781127428	snp	C/G	3.50085e-05	0.00418366	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706377	CCGACTCCTCCGGCT[C/G]CCGAGGCCATGGCGG	9972
rs781146710	snp	C/T	1.65436e-05	0.00287602	synonymous-codon	NUP153	GRCh38.p7	6:17649163	ATAATGGTTTTGTAC[C/T]TTGTTTGTTAATGCT	9972
rs781189641	snp	C/T	4.98691e-05	0.0049932	synonymous-codon	NUP153	GRCh38.p7	6:17628725	AGATTCCTTCTCAGA[C/T]GGTTTTGTCATACTA	9972
rs781201048	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17659939	CTCCCTTCACAACAC[A/T]CTAGTAGAGTGAGAA	9972
rs781203762	snp	A/G	1.65976e-05	0.00288072	synonymous-codon	NUP153	GRCh38.p7	6:17629274	ATTATCATTCTTACT[A/G]TCTTTTTTAACTTCT	9972
rs781204338	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	NUP153	GRCh38.p7	6:17637460	GCCTATCACTGGTTT[A/G]AATTTGTCTCCAAAG	9972
rs781214196	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17699596	AATCCCAGCACTTTG[A/G]GAAGCCGAGGAGGGC	9972
rs781217512	snp	C/G	1.74616e-05	0.00295474	missense, intron-variant	NUP153	GRCh38.p7	6:17668998	TTTTGGCCTGAAAAT[C/G]TGTGATATCTATCCC	9972
rs781281293	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17648581	AAGATCGTGCCACTG[C/T]ACTCCAGCCTGGGTG	9972
rs781285295	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17636154	GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	9972
rs781306147	snp	A/G	1.68247e-05	0.00290035	intron-variant	NUP153	GRCh38.p7	6:17669259	AATTTTTGTATGAAC[A/G]ATATTTTGTAAAAAG	9972
rs781308536	snp	G/T	1.64928e-05	0.00287161	utr-variant-3-prime	NUP153	GRCh38.p7	6:17616073	CAGCTGTTGTTAAAA[G/T]TGAGTACAACACCAA	9972
rs781328490	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17700416	TCAGGCTGACTCCAT[C/T]ACACTACAATGTTTT	9972
rs781331653	snp	A/G	1.67276e-05	0.00289197	missense, nc-transcript-variant, upstream-variant-2KB	NUP153, LOC105374952	GRCh38.p7	6:17706314	TGGTAAGGCTTAATT[A/G]GCCCCTGGTGGCAAC	9972
rs781396935	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708662	CTGTTTCTAAGCTTC[A/G]TTTTTTTCATCAGCA	9972
rs781430553	snp	C/T	7.02543e-05	0.0059264	intron-variant, downstream-variant-500B	NUP153	GRCh38.p7	6:17632613	CTTACAAAAAGGCGC[C/T]TTACCATCACCTTTA	9972
rs781464355	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17628058	AAATTCTAGTTCACT[A/C]ATCTGATTATCAGCT	9972
rs781481651	snp	A/G	1.65094e-05	0.00287305	intron-variant	NUP153	GRCh38.p7	6:17626206	CATAAATCCTTAAGA[A/G]TAGTCTCAGAAAGTA	9972
rs781507346	snp	A/G	1.6863e-05	0.00290365	intron-variant	NUP153	GRCh38.p7	6:17669598	AAATCTAAGGCACAT[A/G]TTTCATGCAGTGAAA	9972
rs781531979	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17659636	CGCTATCACACCCAG[A/C]TAATTTTTGTATTTT	9972
rs781543430	snp	A/G	1.64784e-05	0.00287035	synonymous-codon	NUP153	GRCh38.p7	6:17675669	ATGGCTGACAGTGTA[A/G]TGCAGGGGATTCCAA	9972
rs781563118	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17674096	TTACATATGACTAAA[C/T]GTATATGACATTCTG	9972
rs781567726	in-del	-/GTCAAAGAAAGG			intron-variant	NUP153	GRCh38.p7	6:17690675	GATTTCAAAGAAAGA[-/GTCAAAGAAAGG]AAAAAAATGACTCAG	9972
rs781579370	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17660235	TTGTTTCTGTCAATA[C/T]AAATAGGAAAAGCAT	9972
rs781579969	in-del	-/CGAG			intron-variant	NUP153	GRCh38.p7	6:17703151	GCAGTGAGCCAAGAT[-/CGAG]CGAGCCACTGCACTC	9972
rs781582953	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17639801	GCAAAAGAATTACAC[C/G]TAACTACATCTCTAT	9972
rs781634251	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17679362	CTACAAAACAGTACC[A/G]AAAGAAAGAAAACAG	9972
rs781671591	snp	C/T	1.64749e-05	0.00287005	missense	NUP153	GRCh38.p7	6:17661717	ATCTTGCCACCTCCA[C/T]CACCTACTCCAGAAG	9972
rs781683737	in-del	-/T	0.00118367	0.0242988	intron-variant	NUP153	GRCh38.p7	6:17628616	ACAACTTGTAAAAAA[-/T]AAAAATAATAATAAT	9972
rs781687944	snp	A/G	1.64738e-05	0.00286995	missense	NUP153	GRCh38.p7	6:17624657	CTGTCCCAAAAGTAG[A/G]TGGTGCAGGCTGAGA	9972
rs781698400	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17627399	AATTTTGAGTGTTTC[C/T]AATTTATTATTCAAA	9972
rs781710715	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17639008	GGACACATCTGGTGG[A/G]TACGTTTAAATTCTT	9972
rs781749816	snp	C/T	1.65496e-05	0.00287655	intron-variant	NUP153	GRCh38.p7	6:17661634	TAAACCTCAAGAGTA[C/T]ATGAGTATACAACCC	9972
rs796132779	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17678963	AAAAAAAAAAAAAAA[-/A]TAAGTCTTAACAAAT	9972
rs796157685	in-del	-/ATA			intron-variant	NUP153	GRCh38.p7	6:17654878	GAGATATATGGCATA[-/ATA]CCATACAGCTATTAA	9972
rs796179536	in-del	-/T			intron-variant	NUP153	GRCh38.p7	6:17699203	AATTTTTTTTTTTTT[-/T]AAATACAAGCTAGCT	9972
rs796190107	in-del	-/GG			intron-variant	NUP153	GRCh38.p7	6:17681402	CCATCCTGGCTAACA[-/GG]TGAAACCCCGTGTCT	9972
rs796216145	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17701676	AAAAAAAAAAAAAAA[-/A]TACAAAAATTAGCTA	9972
rs796218509	snp	A/G			upstream-variant-2KB, nc-transcript-variant	NUP153, LOC105374952	GRCh38.p7	6:17707034	CCGCGCGGCACGCTG[A/G]GAAACGTAGTTCAAC	9972
rs796222760	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17655557	CTCCCAGGTTCAAGC[A/G]ATTCTTCTGCCTCAG	9972
rs796246084	snp	C/G			intron-variant	NUP153	GRCh38.p7	6:17676144	AAATAAGTTTTACCC[C/G]TATTTTGATACTGTT	9972
rs796250960	in-del	-/AAAAAAAAAAAA			intron-variant	NUP153	GRCh38.p7	6:17620096	GAGCAAGACACCATC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAG	9972
rs796266516	in-del	-/TT			intron-variant	NUP153	GRCh38.p7	6:17618563	AAGTTAAAATCTCTC[-/TT]TTTTTTTTTTTTTTT	9972
rs796359489	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17633697	GCACAGGAAGAACGG[C/T]TTGGTAAGGCCCAAA	9972
rs796383661	snp	A/G			upstream-variant-2KB, intron-variant	NUP153, LOC105374952	GRCh38.p7	6:17708414	GAGTGCAATGGCGCA[A/G]TCTCAGCAACCTCCA	9972
rs796391588	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17681223	CTTTAAAAAAAAAAA[-/A]CGGACTCAAAAGAAC	9972
rs796400107	in-del	-/ACACACAC			intron-variant	NUP153	GRCh38.p7	6:17693184	ATTTAGCTTTTTCCT[-/ACACACAC]ACACACACACACACA	9972
rs796452534	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17673485	TCTCAAAATTTATTA[A/G]TAAGAAAATAACCCA	9972
rs796458364	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17620121	AAAAAAAAAAAAAAA[-/A]GGAAGGGAGGGAGGA	9972
rs796472667	snp	A/T			intron-variant	NUP153	GRCh38.p7	6:17666003	TTTTTTTTTTTTTTT[A/T]AAATGGAGACTAGGT	9972
rs796481524	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17701846	TCGGGGGGGGGGGGA[A/G]AAAAGCTAAATGCAG	9972
rs796487421	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17623376	AAAAAAAAAAAAAAA[-/A]CCTTTTAAAACAATT	9972
rs796505512	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17634991	AAATAAAAAAAAAAA[-/A]TAAATCGCAAAAGAA	9972
rs796567924	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17694992	TCAAGGAAAAAAAAA[-/AA]GAGAGAGTGGGAAGT	9972
rs796579282	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17635012	CGCAAAAGAATCTCA[C/T]AATGTTTTAGAAAAT	9972
rs796611436	snp	A/C			intron-variant	NUP153	GRCh38.p7	6:17692917	TTCTTGAAAGGCTTA[A/C]TCTTCAGTTATCTAG	9972
rs796621157	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17703669	TTAAAAAAAAAAAAA[-/A]GGAGAGTATTCTTTT	9972
rs796672373	in-del	-/AC			intron-variant	NUP153	GRCh38.p7	6:17632863	AAAAAAAAAAAAAAA[-/AC]GGGGAGTGGGGGGAG	9972
rs796778404	snp	C/T			utr-variant-3-prime	NUP153	GRCh38.p7	6:17615755	ATGAACGCTTATCAG[C/T]GCACATAATGGTGTA	9972
rs796796333	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17672326	TTCATGCTTGTAATC[C/T]GAACACTTTGGGAAG	9972
rs796819993	snp	C/T			intron-variant	NUP153	GRCh38.p7	6:17623828	TTTTCTAGGGATGCA[C/T]CTATTAGCCAATAAA	9972
rs796899937	snp	A/G			intron-variant	NUP153	GRCh38.p7	6:17630744	GAGGGGAGAGGGGAG[A/G]GGAGAAGGGAGGGGA	9972
rs796913317	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17682926	GTCTCAAAAAAGAAG[-/A]AAAAAAAAAAAAAAA	9972
rs796953279	in-del	-/AA			intron-variant	NUP153	GRCh38.p7	6:17628611	AAAACGACAACTTGT[-/AA]AAAAAAAAATAATAA	9972
rs797013631	in-del	-/A			intron-variant	NUP153	GRCh38.p7	6:17696009	GTGAGACTCCGTCTC[-/A]AAAAAAAAAACAGAA	9972

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