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

CUEDC2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs12558	snp	A/C/T	1.65721e-05	0.0028785	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423397	CTCTGCCCGAGCCTT[A/C/T]TAGGCTCAGATCCCA	79004
rs1044476	snp	C/T	0.188828	0.242401	synonymous-codon	CUEDC2	GRCh38.p7	10:102424324	GCCCCTGCAGCGGCC[C/T]GAAATGCTCAAAGAA	79004
rs1409312	snp	A/G	0.217851	0.247924	intron-variant	CUEDC2	GRCh38.p7	10:102432043	GCTTCACAGGGGCTG[A/G]GAGAAGCAGTGAAGA	79004
rs1409313	snp	A/G	0.21725	0.247846	intron-variant	CUEDC2	GRCh38.p7	10:102431844	GTCCACAGTGTCTCT[A/G]TCTAGCATCTGGAGG	79004
rs1572530	snp	C/T	0.438666	0.164028	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434077	AGCATAGTATCTTGG[C/T]ACTGCCTTAGTCCCT	79004
rs1572531	snp	A/G	0.198324	0.244601	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433976	CCCAGCACCCCACGA[A/G]GGAACTAGCACTAAA	79004
rs2902543	snp	A/C	0.00993419	0.0697739	intron-variant	CUEDC2	GRCh38.p7	10:102427676	ctcttgcctgcaaga[A/C]cttcctaacccttct	79004
rs3210927	snp	C/T	0.00865784	0.0652224	synonymous-codon	CUEDC2	GRCh38.p7	10:102423806	GCTGAAGTCCTTCAT[C/T]CTGCAGAAGTACATG	79004
rs3837341	in-del	-/C			intron-variant	CUEDC2	GRCh38.p7	10:102432428	CACGGTACCCCCCCC[-/C]GGGGCCCGTCGGACC	79004
rs6584498	snp	A/G	0.00993419	0.0697739	intron-variant	CUEDC2	GRCh38.p7	10:102428478	GAGCACCTAGCCAGC[A/G]CGGGCATTTTTCTAG	79004
rs6584499	snp	G/T	0.419616	0.183658	intron-variant	CUEDC2	GRCh38.p7	10:102428502	TTTCTAGGTGCTAGG[G/T]TACACAAACTATTTC	79004
rs7074566	snp	A/G	0.0345262	0.126772	intron-variant	CUEDC2	GRCh38.p7	10:102430047	tcaggtgatctgccc[A/G]ccttggcctcccaaa	79004
rs7081280	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432731	TATGGACGGGCTCCC[G/T]TGGCGGCCAGTTTTG	79004
rs7894593	snp	A/G	0.109108	0.206518	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434324	AGGCTGCAGTAAGCC[A/G]TGATTGTGCTACTGC	79004
rs7921010	snp	G/T	0.318174	0.240525	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433069	tagctgggattacag[G/T]cgcgcgccaccacgc	79004
rs9665587	snp	A/C	0.438946	0.163706	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432810	TCGAAGTGGGTAGGA[A/C]TGCATCCCCGTCTTG	79004
rs10654228	in-del	-/T/TT	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430144	TCTTTTTTTTTTTTT[-/T/TT]AATTTTATTTATTTA	79004
rs11352968	in-del	-/A	0.425894	0.177655	intron-variant	CUEDC2	GRCh38.p7	10:102429022	GTGAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	79004
rs11398443	in-del	-/CCT/T	0.499121	0.020948	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432910	CTCTCTCTCTCTCAC[-/CCT/T]TTTTTTTTCCTTTTC	79004
rs11440410	in-del	-/C	0.222035	0.248431	intron-variant	CUEDC2	GRCh38.p7	10:102430646	ACATCCTCCCTCCCT[-/C]CCTCCTGTTTTTGGT	79004
rs11550025	snp	C/T	0.000415769	0.0144122	missense	CUEDC2	GRCh38.p7	10:102424286	GGTCTTCGGCTGCTG[C/T]TGCTGCAGACACCCA	79004
rs11592718	snp	C/T	0.283158	0.247791	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432934	CCTTTTCTTCTTCTT[C/T]TTTTTTTTTGGGAGG	79004
rs11593146	snp	A/G	0.450022	0.149989	intron-variant	CUEDC2	GRCh38.p7	10:102425224	ACAGACAGGATGGCC[A/G]GGCCTTCTTCTGCCT	79004
rs11594302	snp	A/G	0.190205	0.242744	intron-variant	CUEDC2	GRCh38.p7	10:102427072	gatctacaaaaaaaa[A/G]ggggggaatttctca	79004
rs11595402	snp	A/G	0.5	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434396	AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAAAGA	79004
rs11597439	snp	C/G	0.450872	0.14883	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102425196	AGCTCCATGCTCTCT[C/G]TTCTGAAGGGACACA	79004
rs12360467	snp	C/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434038	TCACAGTCCAAGAGA[C/G]AAGTCCCATCTTTCC	79004
rs12415921	snp	G/T	0.196149	0.244131	intron-variant	CUEDC2	GRCh38.p7	10:102432012	AGGGAGGCAGCAAGG[G/T]GTCTAGCATGGAAGG	79004
rs12569389	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102428806	agggggttggatcac[C/G]aggtcaggagatcaa	79004
rs12778231	snp	C/T	0.237905	0.249707	intron-variant	CUEDC2	GRCh38.p7	10:102424432	CAGGTTTGCCAAGGC[C/T]CTGGGGAGCAGGCAG	79004
rs17855346	snp	A/C			stop-gained	CUEDC2	GRCh38.p7	10:102423695	GAATCTTCTGATCCT[A/C]TGCGCTATCCACCAT	79004
rs28686884	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430254	GCTCACCGCAACCTC[A/C]ACCTCCTGGGTTCAA	79004
rs34608648	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102429997	TAGAGACGGGGTTTC[A/C]CCATGTTGGCCAGGC	79004
rs35950389	in-del	-/C			intron-variant	CUEDC2	GRCh38.p7	10:102430766	CTAATACTTCTCCCC[-/C]GCATAGCCCCTGAGT	79004
rs41287462	snp	A/G	0.36075	0.22413	intron-variant	CUEDC2	GRCh38.p7	10:102424456	CAGGCAGTTGGGGGA[A/G]CGGGATTATGAATCA	79004
rs55659266	in-del	-/T	0.114036	0.209795	intron-variant	CUEDC2	GRCh38.p7	10:102429822	AGCCCAGTTTCTTTC[-/T]TTTTTTTTTTTTTTG	79004
rs55824105	in-del	-/A			intron-variant	CUEDC2	GRCh38.p7	10:102429037	AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAATATT	79004
rs57965979	in-del	-/AAAAA	0	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434398	AAAAAAAAAAAAAAA[-/AAAAA]GAAGAAGAAAAGAAG	79004
rs59973108	in-del	-/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434396	AAAAAAAAAAAAAAA[-/G]AAGAAGAAGAAAAGA	79004
rs60025237	snp	C/G/T	0.0017033	0.0291338	downstream-variant-500B, synonymous-codon, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422808	TCCTCCCTCAGGACA[C/G/T]TGGCCGAGTACTGCC	79004
rs60312809	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434147	TGAGGTGGGAGGATC[A/G]CTTGAGCCCAGGAAT	79004
rs61031688	in-del	-/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433471	TTTTTTTTTTTTTTT[-/T]GTAGAGACAGGGTTT	79004
rs61873665	snp	A/G	0.109461	0.206758	intron-variant	CUEDC2	GRCh38.p7	10:102430095	ATGAGCCACCTGTGT[A/G]GTGGTGACTGAAACT	79004
rs71016379	in-del	-/T	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102429037	AATATTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	79004
rs71016380	in-del	-/TAAA	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430167	AGTAAAATAAATAAA[-/TAAA]TAAATAAATAAATAA	79004
rs71948033	in-del	-/TTTA			intron-variant	CUEDC2	GRCh38.p7	10:102430168	TATTTATTTATTTAT[-/TTTA]TTATTTATTTTACTT	79004
rs72845696	snp	C/T	0.28578	0.247426	intron-variant	CUEDC2	GRCh38.p7	10:102427647	TCTCCATCTCTACTC[C/T]CACTTTTCTCCATCT	79004
rs74608233	snp	A/C	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102429023	TGAGACTTTGTCTCA[A/C]AAAAAAAAAAAAAAG	79004
rs75659956	in-del	-/C	0.0603597	0.1629	intron-variant	CUEDC2	GRCh38.p7	10:102432014	GAGGCAGCAAGGGGT[-/C]CTAGCATGGAAGGTC	79004
rs76297957	snp	C/G	0.0248432	0.108648	intron-variant	CUEDC2	GRCh38.p7	10:102426407	TCATAGACTACTGAT[C/G]TGCGCACATCCCCCT	79004
rs76691226	snp	G/T	0.5	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433984	TAGTTCCTTCGTGGG[G/T]TGCTGGGGACCCGGA	79004
rs76802044	snp	G/T	0.5	0	intron-variant	CUEDC2	GRCh38.p7	10:102429834	TTCTTTTTTTTTTTT[G/T]TTGAGACGGAGTTTC	79004
rs77579852	snp	C/G	0.0248432	0.108648	intron-variant	CUEDC2	GRCh38.p7	10:102425637	AAGCACAGCCCTTCC[C/G]CCACCCAGAACAGGC	79004
rs78678650	snp	A/G	0.0991586	0.199366	intron-variant	CUEDC2	GRCh38.p7	10:102430767	CTAATACTTCTCCCC[A/G]CATAGCCCCTGAGTT	79004
rs79317042	snp	A/C	0	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434374	AGCAAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA	79004
rs80152299	snp	A/G	0.030665	0.119967	intron-variant	CUEDC2	GRCh38.p7	10:102430746	ATCCTTCCTGCTCAG[A/G]GGCTCCTAATACTTC	79004
rs80160917	snp	A/G	0.0310518	0.120672	intron-variant	CUEDC2	GRCh38.p7	10:102431856	AGATAGAGACACTGT[A/G]GACAAATTTAAGTGA	79004
rs111910906	snp	C/G/T	0	0	splice-acceptor-variant	CUEDC2	GRCh38.p7	10:102423718	TCCACCATCATGTAC[C/G/T]TGTCAAAAACTGGCT	79004
rs112673733	snp	G/T	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102430208	AGTTTCACTCTTGTT[G/T]CCCAGGCTAGAGTGC	79004
rs114399613	snp	C/T	0.0248432	0.108648	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433847	ATTCCCGGTGCTGCC[C/T]TGTGGGGAAGCCCCA	79004
rs114489414	snp	C/T	0.00755907	0.0610114	intron-variant	CUEDC2	GRCh38.p7	10:102432051	GCTTCTCCCAGCCCC[C/T]GTGAAGCCCGGTTCC	79004
rs114914917	snp	A/T	0.0248432	0.108648	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433495	AGGGTTTTTGCCACG[A/T]GGCCCAGGCTGGTCT	79004
rs117106761	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430458	ATAGGCGTGAGCCAC[C/T]GTGCCCGGCCTGAGA	79004
rs117107179	snp	C/T	0.00199481	0.0315187	intron-variant	CUEDC2	GRCh38.p7	10:102425937	CCTGCGGGACATCCA[C/T]GGCTCGTCCAGTCAC	79004
rs117878070	snp	A/T	0.013466	0.0809424	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423004	TCTGACCCGCCTGCC[A/T]ATCGGAGCACAGCTG	79004
rs138190749	snp	C/T	6.62427e-05	0.00575473	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423632	CCACCCATTCCGCAT[C/T]CCCAGCAACCCTTAA	79004
rs138763107	snp	A/G	0.0107246	0.0724382	intron-variant	CUEDC2	GRCh38.p7	10:102426953	CAGCCATGAGTCACC[A/G]TGCCCGGCCTCAAAA	79004
rs138779369	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433366	GGCTCACTGCAGCCC[C/T]GACCTCCTGGGTTCA	79004
rs139005407	snp	C/T	0.0023933	0.0345097	intron-variant	CUEDC2	GRCh38.p7	10:102428767	GGAGGCTCATGCCTG[C/T]AATCCCAGCACTTTG	79004
rs139747085	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429741	GGGTTACATCACCCT[C/T]GAATCCTGGGCTGTC	79004
rs140083599	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430943	AGAGATCATTGGTTG[A/G]TGGTGTCTACCAAAT	79004
rs140462766	snp	A/C	0.00517822	0.0506191	intron-variant	CUEDC2	GRCh38.p7	10:102431343	GAGACGGGGTTTCAC[A/C]ATGTTGGCCAGACTG	79004
rs141067478	snp	G/T	0.000102513	0.00715862	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422865	CACTGCCACCATGTG[G/T]CGGAGTCCAGCCTGA	79004
rs141182150	snp	C/G	0.00597247	0.0543191	intron-variant	CUEDC2	GRCh38.p7	10:102428333	ATCATCTGAGTGGGA[C/G]AATGAGCTGCCATTT	79004
rs141221578	in-del	-/CTTT			intron-variant	CUEDC2	GRCh38.p7	10:102427191	ATTTCTTCGAAGGCC[-/CTTT]CTTTCTCTGTCCCCT	79004
rs142262811	snp	A/G	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102432207	AGCACAAACAGGGAG[A/G]GCGAGCACAGGAAGT	79004
rs142302379	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431191	GCCATCCAGGCTGGA[A/G]TGCAGTGGTGCGATC	79004
rs142869292	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430249	TCTTGGCTCACCGCA[A/C]CCTCCACCTCCTGGG	79004
rs143090336	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430211	TTCACTCTTGTTGCC[A/C]AGGCTAGAGTGCAAT	79004
rs143479353	snp	A/C	0.0134861	0.0810011	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434511	TCCTTCCTCTTCTGG[A/C]CTCAGAGACAGCAAG	79004
rs143589722	snp	A/G	0.00352149	0.0418132	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423628	AGTCCCACCCATTCC[A/G]CATCCCCAGCAACCC	79004
rs143655912	snp	C/G	0.00165683	0.0287345	intron-variant	CUEDC2	GRCh38.p7	10:102424594	TGAGAGGATGACTCT[C/G]CCCACCCCATAATCA	79004
rs144013189	in-del	-/CT			intron-variant	CUEDC2	GRCh38.p7	10:102427273	CTTCTCACTGCAGCG[-/CT]CTCTCTCTCTCTGGA	79004
rs144450686	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429944	GCTGGGATTACAGGC[A/G]CCTGCCACAACGCCC	79004
rs145290548	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430180	TTATTTATTTATTTT[A/C]CTTTTGAGACAGAGT	79004
rs145311924	in-del	-/G			downstream-variant-500B, frameshift-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422959	GCTGCAGGATATGGC[-/G]GGGCTTCGCACCTTT	79004
rs145688904	snp	A/G	4.71242e-05	0.00485385	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422904	CGGAAGCGCGGCGTG[A/G]ACATCGACGTGGAGC	79004
rs145943166	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426514	TTTGCCCTCTTTCAC[A/C]CCTACCAGTCAATCA	79004
rs146403832	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429701	CCTCAGGGTAGAACC[A/G]CCTCCAGGGACCTAC	79004
rs147214320	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430212	TCACTCTTGTTGCCC[A/C]GGCTAGAGTGCAATG	79004
rs147652970	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102432076	GGTTCCTGAGGCCCT[A/G]GACCCATAACGCAGG	79004
rs148003733	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434549	CTGCTTGGGGGAGGT[A/G]GCAGGGAAGGAAGGG	79004
rs148221748	in-del	-/ATTTT	0.039522	0.134904	intron-variant	CUEDC2	GRCh38.p7	10:102431121	ACTGTTATTCTCCCC[-/ATTTT]ATTTTATTTATTTTA	79004
rs148855837	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434323	AAGGCTGCAGTAAGC[C/T]GTGATTGTGCTACTG	79004
rs148904455	snp	A/G	0.000976845	0.0220787	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423419	CGGGCAGAGTCCGGC[A/G]AGTGCCTCAATGGAA	79004
rs149435454	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429612	ATTCATACCACCTGC[A/G]CCAGAGCCCTCATGG	79004
rs149977211	snp	G/T	0.00478085	0.0486577	intron-variant	CUEDC2	GRCh38.p7	10:102431380	AACTCCTGACCTCAG[G/T]CAATCCACCCGCCTC	79004
rs150719622	snp	A/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428400	ATGCTCCTGACTCCC[A/T]AACAGACTTTTGGGA	79004
rs151012832	snp	C/G	0.000153988	0.00877328	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422824	TGGCCGAGTACTGCC[C/G]CGTGCTGCGTTCGCT	79004
rs151254319	snp	C/G	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102431298	TCGCATGCCACCATG[C/G]CTGGCAAATTTATTT	79004
rs180971080	snp	A/G	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102431444	CCACCGCGCCCGGCC[A/G]TATTATCCACATTTT	79004
rs181460858	snp	C/T	0.00755907	0.0610114	intron-variant	CUEDC2	GRCh38.p7	10:102429849	TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG	79004
rs182370017	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102428893	TGGGTGTGGTGGCAC[A/G]CGCCTGTAGTCCCAG	79004
rs182471058	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430396	CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCT	79004
rs182661552	snp	A/G	0.00132086	0.0256649	intron-variant	CUEDC2	GRCh38.p7	10:102424193	CCTAAGGGTACAAAC[A/G]TTAACAAGAGGCAAT	79004
rs182674950	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423152	TCTTGCCTGGTGCTG[C/G]CCTGTTGAAGATAGG	79004
rs182785080	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433607	CAGGTCTGTGTCTCC[A/G]GAGGGTGGAGCCTGG	79004
rs183001797	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425310	ACCATCTGTTGATGC[C/T]GCCCTCTCTGTTCCC	79004
rs183223258	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102431797	GCTCCCAGCTAGCCT[A/G]GGAGCTTCCCAAGGG	79004
rs184026453	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426781	GACTACAGGCACACA[C/T]CACCTACTAGTTTTT	79004
rs184376685	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428526	CTATTTCCTCTGCCT[A/G]GGCACCCTTCTGCCT	79004
rs184525221	snp	A/T	0	0	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434211	GTCTCTACAAAAAAT[A/T]TAAAAAATAAAAAAT	79004
rs184943572	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434498	CCTCACAACAGCCTC[A/C]TTCCTCTTCTGGCCT	79004
rs185510913	snp	C/G	1.65605e-05	0.0028775	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423635	CCCATTCCGCATCCC[C/G]AGCAACCCTTAACTC	79004
rs185754900	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429983	TTTTGTATTTTTGGT[A/G]GAGACGGGGTTTCAC	79004
rs186018556	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431711	CCCAGAGCATCTGTC[C/T]CTCTGCCTCTCCAAA	79004
rs186042998	snp	C/G/T	2.38007e-05	0.00344961	intron-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422788	TGTCCCTAGCCTCAC[C/G/T]CTGCTCCTCCCTCAG	79004
rs186283090	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429566	GGTCACTTTGGAAAG[A/C]AGGACTGAGAAGCCC	79004
rs187335593	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425733	TGGATTCTCTCTTCT[C/T]GCCCAGTCCCTGCCC	79004
rs187861039	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434328	TGCAGTAAGCCGTGA[C/T]TGTGCTACTGCACTC	79004
rs188094826	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433730	CCTACCCCCCGGGGC[C/T]TTCATCCCCCATGTT	79004
rs188851626	snp	C/G/T	0.000787611	0.0198296	intron-variant	CUEDC2	GRCh38.p7	10:102424216	GAGGCAATACTCCCC[C/G/T]CTTTCCAGCCCCCTG	79004
rs189093418	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102429671	CCAGGCATACTAGAT[C/T]CCATCATGCAGCTCC	79004
rs189712895	snp	C/T	0	0	intron-variant	CUEDC2	GRCh38.p7	10:102426995	GAGGTCATCAGTTAC[C/T]TTTTCCAGGTTTTAG	79004
rs190533541	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102428805	CAGGGGGTTGGATCA[C/T]GAGGTCAGGAGATCA	79004
rs190566574	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432686	ACAACAGGGCGGAGC[G/T]CCTGCTCTAATTCTC	79004
rs190809867	snp	A/G	0.00087282	0.0208722	missense	CUEDC2	GRCh38.p7	10:102423847	GGGGGCCTCTGAGGC[A/G]TCTGGGCAGGTCCTG	79004
rs191300611	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431036	ATTGCCTCTGCTTAC[A/G]AGGCATTGTCCTAAG	79004
rs191865721	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426350	TCATCATCCCACTCA[A/G]AAGGCTCCGAGGCAC	79004
rs192094209	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102431782	TGCCCCACCTTCACT[G/T]CTCCCAGCTAGCCTG	79004
rs192409309	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428060	GATTCTCCTGCCTCA[C/G]CCTCCCGAGTAACTG	79004
rs192887431	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434013	GAAGCTGTCCCTGCC[C/T]TCAGGGAGCTCACAG	79004
rs193231734	snp	C/T	0.0008285	0.0203363	synonymous-codon	CUEDC2	GRCh38.p7	10:102424384	ACCAGAGCTCTGCGG[C/T]TGCAGGTTCTCTTAA	79004
rs199505123	in-del	-/C			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432933	CCTTTTCTTCTTCTT[-/C]TTTTTTTTTTGGGAG	79004
rs199625253	snp	A/G	0.000265155	0.0115112	missense	CUEDC2	GRCh38.p7	10:102424329	TGAGCATTTCGGGCC[A/G]CTGCAGGGGCTCTGG	79004
rs199727426	snp	C/G	0.0128186	0.0790252	synonymous-codon	CUEDC2	GRCh38.p7	10:102425144	CGGGAGGTGTGTCTG[C/G]ACAAAGGCAAGGAGG	79004
rs200010505	snp	A/T	4.97236e-05	0.00498591	intron-variant	CUEDC2	GRCh38.p7	10:102423746	GCTGGGTGAAGCTCC[A/T]GTCACCCTGGGAAGA	79004
rs200043796	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430131	GAAAGCCCAGGTTTT[C/T]TTTTTTTTTTTTTAA	79004
rs200060563	snp	C/T	0.000150134	0.00866282	missense	CUEDC2	GRCh38.p7	10:102424075	TCTTCCAAGTCCCCC[C/T]GAGCTTTGGCCAGCA	79004
rs200525665	snp	C/T	5.00697e-05	0.00500323	synonymous-codon	CUEDC2	GRCh38.p7	10:102424110	CTGGGCCTGCTCCAC[C/T]GAACAGGTAGGGAAC	79004
rs200550064	snp	A/G	0.00316662	0.0396646	missense	CUEDC2	GRCh38.p7	10:102424295	GCAGCAGCAGCAGCC[A/G]AAGACCTAGTCTCTT	79004
rs200745080	snp	C/T	0.000399281	0.0141238	synonymous-codon	CUEDC2	GRCh38.p7	10:102423684	CATGGGCCGGTGAAT[C/T]TTCTGATCCTCTGCG	79004
rs200755540	snp	C/T	0.000216936	0.0104125	synonymous-codon	CUEDC2	GRCh38.p7	10:102425129	CCTGAGGTCGGCCTC[C/T]GGGAGGTGTGTCTGG	79004
rs200857395	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432919	CTCTCACTTTTTTTT[C/T]CTTTTCTTCTTCTTT	79004
rs200977019	snp	A/G	5.04927e-05	0.00502432	missense	CUEDC2	GRCh38.p7	10:102423853	CTCTGAGGCGTCTGG[A/G]CAGGTCCTGCAGAGA	79004
rs201123507	snp	A/G	5.11112e-05	0.005055	intron-variant	CUEDC2	GRCh38.p7	10:102423974	CTGAGGCTACATGGT[A/G]GAGGGTGCTGGGAAA	79004
rs201349133	snp	A/G	0.000250926	0.0111982	missense	CUEDC2	GRCh38.p7	10:102424733	TCCTCTGATGGGCCC[A/G]AGGGGCCCAGGTCCT	79004
rs201476465	snp	C/T	1.65877e-05	0.00287986	missense	CUEDC2	GRCh38.p7	10:102424558	ATGTCCCCTATTGTG[C/T]CCCTGAAAAGATGAG	79004
rs201654446	snp	A/G	0.000250721	0.0111936	synonymous-codon	CUEDC2	GRCh38.p7	10:102424170	AAGCTCCTCCTCAGC[A/G]CCAGTTGCCTAAGGG	79004
rs201668460	snp	C/T	0.000969867	0.0219998	intron-variant	CUEDC2	GRCh38.p7	10:102424192	GCCTAAGGGTACAAA[C/T]GTTAACAAGAGGCAA	79004
rs201799406	snp	A/G	0.000546362	0.0165192	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423608	AGTGGCAGAAGCCAG[A/G]AGCCAGTCCCACCCA	79004
rs201856090	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430650	TCCTCCCTCCCTCCT[A/G]CTGTTTTTGGTCTAC	79004
rs202159055	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430646	AACATCCTCCCTCCC[A/G]CCTCCTGTTTTTGGT	79004
rs202242264	snp	C/T	0.000356721	0.0133504	intron-variant	CUEDC2	GRCh38.p7	10:102423882	GAGGGGAGGCCTGGT[C/T]TAGGCCCAAGGGCAC	79004
rs367656275	snp	C/G	3.32845e-05	0.00407936	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102425192	CTCCAGCTCCATGCT[C/G]TCTCTTCTGAAGGGA	79004
rs368222846	snp	A/G			utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432563	CGACTTGTCCCGCGC[A/G]GTGCAGCTCTCATCC	79004
rs368436499	snp	C/T	8.21845e-05	0.0064098	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422866	ACTGCCACCATGTGG[C/T]GGAGTCCAGCCTGAG	79004
rs368438991	snp	G/T	3.32082e-05	0.00407468	intron-variant	CUEDC2	GRCh38.p7	10:102424466	GGGGAGCGGGATTAT[G/T]AATCACTCAGGTGCC	79004
rs368479775	snp	C/T	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102429000	GCACTCCAGCCTGGA[C/T]GACAGAGTGAGACTT	79004
rs368699035	in-del	-/TCTC			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432905	CTCTCTCTCTCTCTC[-/TCTC]ACTTTTTTTTCCTTT	79004
rs369016562	snp	A/G	0.000530979	0.0162852	synonymous-codon	CUEDC2	GRCh38.p7	10:102424663	CCTGGGGATGTGGGC[A/G]AAGCCAGGCACATAG	79004
rs369045282	snp	C/T	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102428512	CTAGGGTACACAAAC[C/T]ATTTCCTCTGCCTGG	79004
rs369082365	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102427594	CTCATCCAATCAGTC[A/G]CCAAGCCCTAATCAT	79004
rs369132959	in-del	-/CC			upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434595	TTGCCCATAAAAACA[-/CC]CTGCCACTCCAGCCT	79004
rs369284645	snp	A/G	0.000193981	0.00984647	intron-variant	CUEDC2	GRCh38.p7	10:102425063	CCCATAGTACTGCCC[A/G]GCAGCTCCAGCTCCA	79004
rs369567008	snp	C/T	8.39567e-05	0.00647853	missense	CUEDC2	GRCh38.p7	10:102423849	GGGCCTCTGAGGCGT[C/T]TGGGCAGGTCCTGCA	79004
rs369635115	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102425298	GCCTGCTATGGAACC[A/G]TCTGTTGATGCTGCC	79004
rs369827852	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426958	ATGAGTCACCGTGCC[C/T]GGCCTCAAAATTTCT	79004
rs369900351	in-del	-/TTTA/TTTATTTA/TTTATTTATTTATTTA			intron-variant	CUEDC2	GRCh38.p7	10:102430147	TTTTTTTTTTTTAAT[lengthTooLong]TTTATTTATTTATTT	79004
rs369981199	snp	A/C	0.000347939	0.0131852	intron-variant	CUEDC2	GRCh38.p7	10:102423944	GTTGGGGCTTAACAC[A/C]AAGGTGGAATGTAGC	79004
rs370018191	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426101	CCTATTGTCTGTCTG[C/T]CCCCATAAAATGGAA	79004
rs370116180	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431590	CCACACTACATCACC[C/T]CTCACGATGCAAATT	79004
rs371178074	snp	C/T	6.76579e-05	0.00581587	intron-variant	CUEDC2	GRCh38.p7	10:102425097	CTGACATGAGCCTTC[C/T]GGGGGACCCGTCTCT	79004
rs371185904	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429666	TCAGCCCAGGCATAC[C/T]AGATCCCATCATGCA	79004
rs371255049	snp	A/T			intron-variant	CUEDC2	GRCh38.p7	10:102430146	CTTTTTTTTTTTTTA[A/T]TTTTATTTATTTATT	79004
rs371351565	in-del	-/CCCCACTCCATCTTCC	0.0111196	0.0737302	intron-variant	CUEDC2	GRCh38.p7	10:102427691	CTTCCTAACCCTTCT[-/CCCCACTCCATCTTCC]CCCCACTCCATCTTC	79004
rs371431929	in-del	-/T/TT/TTT			intron-variant	CUEDC2	GRCh38.p7	10:102430131	AAAGCCCAGGTTTTC[-/T/TT/TTT]TTTTTTTTTTTTTAA	79004
rs371683002	snp	A/C	1.65734e-05	0.00287862	synonymous-codon	CUEDC2	GRCh38.p7	10:102424369	CACCTGACCTTGGAC[A/C]CCAGAGCTCTGCGGT	79004
rs371740123	in-del	-/G			intron-variant	CUEDC2	GRCh38.p7	10:102429038	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAATATTT	79004
rs371820534	snp	C/T	0.000750519	0.0193571	synonymous-codon	CUEDC2	GRCh38.p7	10:102423827	GGACTTCAGCTCATC[C/T]TTTTGGGGGCCTCTG	79004
rs371881231	snp	C/G	0.0158469	0.0875917	intron-variant	CUEDC2	GRCh38.p7	10:102430256	TCACCGCAACCTCCA[C/G]CTCCTGGGTTCAAGC	79004
rs372005158	snp	C/T	4.96783e-05	0.00498364	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423499	TCGGCCTCAGGGTTC[C/T]GCACATCTTTGAATC	79004
rs372301009	snp	A/C/T	3.38766e-05	0.00411551	intron-variant	CUEDC2	GRCh38.p7	10:102425227	GACAGGATGGCCAGG[A/C/T]CTTCTTCTGCCTGCC	79004
rs372449595	snp	C/T	0.000159987	0.00894249	synonymous-codon	CUEDC2	GRCh38.p7	10:102424524	GGCATCGCTCAGCTG[C/T]CCTGAGAGCTTCTGC	79004
rs372555860	snp	C/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432786	TGAAGGTCTTGAGAG[C/G]GGGTGGAGTCGAAGT	79004
rs373065366	snp	A/C/T	3.32901e-05	0.0040797	missense	CUEDC2	GRCh38.p7	10:102424705	CTCAGTGAAAGCCTC[A/C/T]ATATCGAAGTTCTCC	79004
rs373178334	snp	A/C			missense	CUEDC2	GRCh38.p7	10:102424140	CACCTCCAGGAGTAC[A/C]TCCACCCCTGGCAGA	79004
rs373431726	snp	A/C/G	8.39872e-05	0.0064798	intron-variant	CUEDC2	GRCh38.p7	10:102425107	CCTTCCGGGGGACCC[A/C/G]TCTCTACCTGAGGTC	79004
rs373460233	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433420	TGGAGTAGCTGGAAC[C/T]ACAGGCGCGTGCCAC	79004
rs373664707	snp	A/T	0.000188409	0.00970408	intron-variant	CUEDC2	GRCh38.p7	10:102425069	GTACTGCCCGGCAGC[A/T]CCAGCTCCAGCACTG	79004
rs373873420	snp	A/G	0.00013342	0.00816653	missense	CUEDC2	GRCh38.p7	10:102424054	TCTACCAGCATCTGC[A/G]CAGCTTCTTCCAAGT	79004
rs374014199	snp	G/T	5.01634e-05	0.00500791	intron-variant	CUEDC2	GRCh38.p7	10:102425217	AAGGGACACAGACAG[G/T]ATGGCCAGGCCTTCT	79004
rs374054435	snp	C/T	1.65773e-05	0.00287895	synonymous-codon	CUEDC2	GRCh38.p7	10:102424381	GACACCAGAGCTCTG[C/T]GGTTGCAGGTTCTCT	79004
rs374348913	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102429180	CTAGCAGCACCTTTC[A/C]CAGCCATAATTATTA	79004
rs374441057	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431443	ACCACCGCGCCCGGC[C/T]GTATTATCCACATTT	79004
rs375086501	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102424848	GATGCCTCCAGCACC[C/G]CCACCTATCCTGAGA	79004
rs375489776	snp	A/G	1.70635e-05	0.00292087	intron-variant	CUEDC2	GRCh38.p7	10:102423893	TGGTCTAGGCCCAAG[A/G]GCACCAGCAGGGGAA	79004
rs375536311	snp	C/G	1.67556e-05	0.0028944	intron-variant	CUEDC2	GRCh38.p7	10:102424232	CTTTCCAGCCCCCTG[C/G]GTCCCTCATCGGTAC	79004
rs376316530	snp	A/G	0.000250369	0.0111858	missense	CUEDC2	GRCh38.p7	10:102424150	AGTACATCCACCCCT[A/G]GCAGAAGCTCCTCCT	79004
rs376711763	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425420	AGCCTCTAGAGGAGG[C/T]GCCCCCCCACCTCTC	79004
rs376831144	snp	C/T	1.71328e-05	0.00292679	intron-variant	CUEDC2	GRCh38.p7	10:102425071	ACTGCCCGGCAGCTC[C/T]AGCTCCAGCACTGAC	79004
rs376890746	snp	C/T	1.70278e-05	0.00291781	intron-variant	CUEDC2	GRCh38.p7	10:102424796	TCATCCAAGCCACTG[C/T]AGGAAGGGAACAGGA	79004
rs377346173	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428970	GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG	79004
rs377444631	snp	A/G	3.34169e-05	0.00408746	synonymous-codon	CUEDC2	GRCh38.p7	10:102425123	TCTCTACCTGAGGTC[A/G]GCCTCCGGGAGGTGT	79004
rs377478397	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102428660	AGGCTGAGGCAAGAG[A/G]ATCGTTTGAGCTCAG	79004
rs377610165	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102428290	CTCTTTCATGGCAAG[A/G]TAGTATACCCTCTGA	79004
rs377751415	snp	A/T			intron-variant	CUEDC2	GRCh38.p7	10:102430145	TCTTTTTTTTTTTTT[A/T]ATTTTATTTATTTAT	79004
rs377763094	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431253	CAAGCAATTCCCCTG[C/T]CTCAGCCTCCTGAGT	79004
rs386372283	in-del	-/TT			intron-variant	CUEDC2	GRCh38.p7	10:102430132	AAGCCCAGGTTTTCT[-/TT]TTTTTTTTTTTTAAT	79004
rs386372284	in-del	-/TT			intron-variant	CUEDC2	GRCh38.p7	10:102430143	TTCTTTTTTTTTTTT[-/TT]TAATTTTATTTATTT	79004
rs386372285	in-del	-/ATTT			intron-variant	CUEDC2	GRCh38.p7	10:102430155	TTTTAATTTTATTTA[-/ATTT]TTTATTTATTTATTT	79004
rs386747098	multinucleotide-polymorphism	ATG/GAC			intron-variant	CUEDC2	GRCh38.p7	10:102428084	GTAACTGGGATTACA[ATG/GAC]ATGTGCACCACACCT	79004
rs397797733	in-del	-/C			intron-variant	CUEDC2	GRCh38.p7	10:102430648	ATCCTCCCTCCCTCC[-/C]TCCTGTTTTTGGTCT	79004
rs397822170	in-del	-/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432917	TCTCTCACTTTTTTT[-/T]TCCTTTTCTTCTTCT	79004
rs397970767	in-del	-/G			intron-variant	CUEDC2	GRCh38.p7	10:102432435	GGGCCCCGGGGGGGG[-/G]TACCGTGGGGGAACA	79004
rs527739224	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426469	CACTCACTCAGCTGC[C/G]AAAGCTGAAACCTGG	79004
rs527865491	in-del	-/CCTT	0.00438332	0.0466095	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433270	TTCTTTCCCTCCCTC[-/CCTT]CCTTCCTTCTCTTTC	79004
rs528146265	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430389	GGTCAGGCTGGTCTC[A/G]AACTCCCGACCTCAG	79004
rs528455467	in-del	-/ATTTTATTT			intron-variant	CUEDC2	GRCh38.p7	10:102430146	TTTTTTTTTTTTTAA[-/ATTTTATTT]TTTTATTTATTTATT	79004
rs528520803	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102428129	TATTTCTAGTAGAGA[C/G]AGGGTTTCACCATGT	79004
rs528715219	snp	C/T	1.65603e-05	0.00287747	missense	CUEDC2	GRCh38.p7	10:102423692	GGTGAATCTTCTGAT[C/T]CTCTGCGCTATCCAC	79004
rs529985656	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102425532	ATGCCTCCTGGCTCA[C/G]GAATCCCATCACTGA	79004
rs531512801	in-del	-/G	0.364817	0.222075	intron-variant	CUEDC2	GRCh38.p7	10:102432427	GGTCCGACGGGCCCC[-/G]GGGGGGGGTACCGTG	79004
rs531567909	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102427185	TCTGGCCATTTCTTC[A/G]AAGGCCCTTTCTCTG	79004
rs531711711	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428477	TGAGCACCTAGCCAG[C/T]ACGGGCATTTTTCTA	79004
rs532258513	snp	C/T	0.00345513	0.0414202	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423468	CTTGAGGTTGATGTA[C/T]GTGGCCTTCATCTCC	79004
rs532483232	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102432045	TTCACTGCTTCTCCC[A/G]GCCCCTGTGAAGCCC	79004
rs532522815	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433092	CACCACGCCCAGATA[A/C]TTTATTGTATTTTTA	79004
rs532839181	snp	C/T	1.67178e-05	0.00289113	missense	CUEDC2	GRCh38.p7	10:102425122	GTCTCTACCTGAGGT[C/T]GGCCTCCGGGAGGTG	79004
rs532981966	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428601	TAAAATTCCCTTCCT[C/T]GGCTGGGCACGGTGC	79004
rs533030060	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429395	CTTGACTGCGGTAGT[A/C]AGATTTAAATCCAGG	79004
rs533398282	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102431163	ATGTATTTTTGAGAC[A/G]GAGTCTCGCTCTGCC	79004
rs533553537	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432599	CCCCACCAACGAGAT[C/G]AAAGGCGGGGCCCAG	79004
rs533563269	snp	A/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432842	TCCTTCTCATCCGTC[A/G]GAGACCCGAAACCTT	79004
rs533754256	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430698	TTCTAAGCTCTTTTA[C/T]CCTTCCCCATCCCCG	79004
rs533950857	snp	A/G	6.64055e-05	0.0057618	intron-variant	CUEDC2	GRCh38.p7	10:102424458	GGCAGTTGGGGGAGC[A/G]GGATTATGAATCACT	79004
rs534058149	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433391	GGTTCAAGTGATCCT[C/G]CCATCTCAGCCTCTG	79004
rs534675812	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431385	CTGACCTCAGGCAAT[C/T]CACCCGCCTCGGTCT	79004
rs534736029	snp	C/T	2.18171e-05	0.00330274	intron-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422795	AGCCTCACCCTGCTC[C/T]TCCCTCAGGACATTG	79004
rs535061506	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425426	TAGAGGAGGCGCCCC[C/T]CCACCTCTCCCCACC	79004
rs535123131	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426733	ATCTCCCCAGCTCAA[C/G]CCATCCTCCTGCCTT	79004
rs536037287	snp	G/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102428756	AGGCCAGGCACGGAG[G/T]CTCATGCCTGTAATC	79004
rs536100200	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102423986	GGTAGAGGGTGCTGG[C/G]AAAAGATACCTGGTT	79004
rs536494667	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433257	TCTTTATTTTCCTTT[A/C]TTTCCCTCCCTCCCT	79004
rs536707162	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428664	TGAGGCAAGAGGATC[A/G]TTTGAGCTCAGGAGT	79004
rs537091515	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430572	TTAGGAAACTCTTCA[C/T]TGTCCCCAAATAAAA	79004
rs537435150	snp	G/T	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102429995	GGTAGAGACGGGGTT[G/T]CACCATGTTGGCCAG	79004
rs537773482	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426571	TTTCCTTCTTATCTG[C/T]ATTGTATCCACTTCT	79004
rs537841479	snp	C/G/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426952	ACAGCCATGAGTCAC[C/G/T]GTGCCCGGCCTCAAA	79004
rs538012799	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433940	AAATTTCCCATCCCC[C/T]ATCAGCAGGGATGAG	79004
rs538101917	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425320	GATGCTGCCCTCTCT[A/G]TTCCCCCAAGTAGAA	79004
rs538399204	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423366	TGTGTAGGGGTATAG[A/G]GCTCCTGCATCCCTC	79004
rs538476416	snp	A/G	0.0310518	0.120672	intron-variant	CUEDC2	GRCh38.p7	10:102428084	GTAACTGGGATTACA[A/G]ACATGTGCACCACAC	79004
rs538865070	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430847	CCACCCTTCTCCAGG[A/G]TAAGAACATGATTTC	79004
rs539023468	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102427695	CCTAACCCTTCTCCC[C/G]ACTCCATCTTCCCCC	79004
rs539083582	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102432276	CCTAAACCCGCTAGC[A/G]GGACACCCGTAAGCG	79004
rs539108818	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426881	GACCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA	79004
rs539706989	snp	A/G	0.00159617	0.0282053	intron-variant	CUEDC2	GRCh38.p7	10:102429892	TGGTGTGAACCTGAC[A/G]GGGTCAAGCAATTCT	79004
rs539736034	snp	C/T	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102429777	CATGGTAGCCTCTGC[C/T]GGGACAAAGGCCCAT	79004
rs539869805	snp	A/G	0.00636936	0.0560724	intron-variant	CUEDC2	GRCh38.p7	10:102428851	ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA	79004
rs540220179	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431828	CAGCACAGGCCTGGA[C/G]CCTCCAGATGCTAGA	79004
rs540278954	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423296	GCAGCTCCGAGAGTA[C/G]GTTAACACTATGGAG	79004
rs540305442	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431152	TTTATTTATTTATGT[A/G]TTTTTGAGACGGAGT	79004
rs540414954	snp	C/T	1.70336e-05	0.00291831	intron-variant	CUEDC2	GRCh38.p7	10:102425083	CTCCAGCTCCAGCAC[C/T]GACATGAGCCTTCCG	79004
rs540496869	snp	C/G	5.01291e-05	0.0050062	missense	CUEDC2	GRCh38.p7	10:102424168	AGAAGCTCCTCCTCA[C/G]CGCCAGTTGCCTAAG	79004
rs540656992	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102426117	CCCCATAAAATGGAA[A/G]CTCCAAAGCAAGGTG	79004
rs540815862	snp	C/T	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102429323	ACAGTTGAACCCCAA[C/T]TTACCTATGAAGAAA	79004
rs540827975	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430046	CTCAGGTGATCTGCC[C/T]ACCTTGGCCTCCCAA	79004
rs541490469	snp	G/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102424913	GACCTTTATCTTTAA[G/T]GCCAGAGAGTATAAC	79004
rs542088309	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426377	GCACCACCAGTTCCA[C/T]GCACCTCACACTCAT	79004
rs542505620	snp	A/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428203	GCCTTGGCCTCCCAA[A/T]GTGCTGGGATTACAG	79004
rs542649199	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430984	TCCTGTCATGAGTCC[C/T]GCCTAAATGCCTCCG	79004
rs542789038	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423109	CCTGCCCCACCCTGG[A/G]GCTTCAAATAAAGAG	79004
rs542803005	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432741	CTCCCTTGGCGGCCA[A/G]TTTTGTTGCGCGTAG	79004
rs542817212	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433606	ACAGGTCTGTGTCTC[A/C]GGAGGGTGGAGCCTG	79004
rs542855091	snp	C/T	3.33985e-05	0.00408633	intron-variant	CUEDC2	GRCh38.p7	10:102424258	GGTACCCTCCTCTAC[C/T]AGTACCTCATCTTGG	79004
rs542910934	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431710	GCCCAGAGCATCTGT[C/T]CCTCTGCCTCTCCAA	79004
rs543636350	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433133	GGTTTCACCATGTTG[G/T]CCAGGCTGGTCTCAA	79004
rs543918496	snp	A/G	1.66026e-05	0.00288115	missense	CUEDC2	GRCh38.p7	10:102424673	TGGGCGAAGCCAGGC[A/G]CATAGGCCTCCATCA	79004
rs543941583	snp	C/G	1.65603e-05	0.00287747	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423486	GGCCTTCATCTCCTC[C/G]GCCTCAGGGTTCCGC	79004
rs544265704	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432707	TCTAATTCTCTAACG[C/T]CCCAGGGCTATGGAC	79004
rs544299212	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428461	GTCAACAAGTATGTA[C/T]TGAGCACCTAGCCAG	79004
rs544336219	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431439	ATGAACCACCGCGCC[C/T]GGCCGTATTATCCAC	79004
rs544461577	snp	A/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426937	CAAAGTGCTGGGATT[A/T]CAGCCATGAGTCACC	79004
rs544624168	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434646	GGGGTGGGGTGACAG[C/T]GACTTTGAACTCTGG	79004
rs544945988	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102430172	TTATTTATTTATTTA[C/T]TTATTTTACTTTTGA	79004
rs545172424	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430808	TGGTCTGCCAGACTG[A/G]TTTCCTAAGTAGCAC	79004
rs545200489	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102424633	CTTCCTCCTCCTGGC[C/G]CTAGCCAGAACCTAC	79004
rs545280242	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431859	TAGAGACACTGTGGA[C/T]AAATTTAAGTGAGAG	79004
rs546250995	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102427080	AAAAAAAAGGGGGGA[A/G]TTTCTCATGATTTCA	79004
rs546597632	snp	A/G	0.00676609	0.0577691	intron-variant	CUEDC2	GRCh38.p7	10:102429033	TCTCAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA	79004
rs546600567	snp	C/G	1.66535e-05	0.00288556	synonymous-codon	CUEDC2	GRCh38.p7	10:102423818	CAGGATGAAGGACTT[C/G]AGCTCATCCTTTTGG	79004
rs546687804	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432981	CCCGGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG	79004
rs546862079	snp	C/T	0.00014949	0.00864424	synonymous-codon	CUEDC2	GRCh38.p7	10:102424294	TGCAGCAGCAGCAGC[C/T]GAAGACCTAGTCTCT	79004
rs546971044	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102432098	TAACGCAGGCCCCAG[A/G]GGATATCATTGTCCT	79004
rs546997764	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102428210	CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAC	79004
rs548289836	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430578	AACTCTTCACTGTCC[C/T]CAAATAAAAAGACTT	79004
rs548327805	snp	A/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432749	GCGGCCAGTTTTGTT[A/G]CGCGTAGGGAGGCGT	79004
rs548354822	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433338	TGGAGTGCAGGTTCA[C/T]GAGTGCGAACATGGC	79004
rs548418111	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434146	CTGAGGTGGGAGGAT[C/T]GCTTGAGCCCAGGAA	79004
rs548591052	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102426359	CACTCAGAAGGCTCC[A/G]AGGCACCACCAGTTC	79004
rs548990997	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430304	CCTCCTGAGTAGCTG[A/G]GATTACAAGCATGTG	79004
rs549700732	snp	A/C	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102427343	ATGTCATCAATTCCC[A/C]AATGTCCAGTCCTCT	79004
rs550076861	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102426574	CCTTCTTATCTGCAT[C/T]GTATCCACTTCTCCC	79004
rs550363754	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428713	ACATATCAAGACCCC[A/G]TCTCTCTTTTTGTAG	79004
rs550520460	snp	A/C	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102432282	CCCGCTAGCGGGACA[A/C]CCGTAAGCGTCCAGA	79004
rs550946332	snp	C/T	0.000364552	0.013496	missense	CUEDC2	GRCh38.p7	10:102424328	TTGAGCATTTCGGGC[C/T]GCTGCAGGGGCTCTG	79004
rs551083972	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428607	TCCCTTCCTTGGCTG[A/G]GCACGGTGCCTCATG	79004
rs551679541	in-del	-/TC	0.0584853	0.160693	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432886	TCTCTCTTTTTCTCG[-/TC]TCTCTCTCTCTCTCT	79004
rs551818044	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430470	CACCGTGCCCGGCCT[C/G]AGAGCCCAGTTTCTA	79004
rs551944984	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431175	GACGGAGTCTCGCTC[C/T]GCCATCCAGGCTGGA	79004
rs552299732	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102430213	CACTCTTGTTGCCCA[G/T]GCTAGAGTGCAATGG	79004
rs552397076	snp	C/T	0.000101597	0.00712657	intron-variant	CUEDC2	GRCh38.p7	10:102425230	AGGATGGCCAGGCCT[C/T]CTTCTGCCTGCCCCC	79004
rs552409146	snp	G/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426506	CCCTTGATTTTGCCC[G/T]CTTTCACCCCTACCA	79004
rs552477418	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434225	TTTAAAAAATAAAAA[A/G]TTATCTGGGCATGGT	79004
rs552490000	snp	A/C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102432347	GCCTTGGAGGACACA[A/C/T]GACGAGGCAGGCCTG	79004
rs552570762	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102431363	TGGCCAGACTGGTCT[C/G]GAACTCCTGACCTCA	79004
rs553225785	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431412	GTCTCCCAAAGTGCT[C/G]GGATTACAGGCATGA	79004
rs553485130	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425453	CACCCCCCTACCTCT[C/T]CCCACCCCCCTACCC	79004
rs553609127	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102427272	CCTTCTCACTGCAGC[A/G]CTCTCTCTCTCTCTG	79004
rs553684419	snp	C/T	0.00398564	0.0444627	intron-variant	CUEDC2	GRCh38.p7	10:102424998	GATGAGAGGTAAGGC[C/T]TCTCAGCAAATCCTA	79004
rs554229821	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428206	TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA	79004
rs554766362	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434534	ACAGCAAGATGTTGG[C/T]TGCTTGGGGGAGGTA	79004
rs554802882	snp	C/G	3.35284e-05	0.00409427	missense	CUEDC2	GRCh38.p7	10:102424010	CCTGGTTGGGGCCCT[C/G]CCAGGCTGCAGGCCC	79004
rs554940634	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432545	TCCGTCGGGCGCCGC[C/T]GGCGACTTGTCCCGC	79004
rs555288595	snp	A/C			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433793	AACTCCAGGGCCCAA[A/C]AAGACTTCAACTTCC	79004
rs555293122	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430582	CTTCACTGTCCCCAA[A/G]TAAAAAGACTTGCTC	79004
rs555479506	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430007	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA	79004
rs555881026	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433527	TTAGGTACTGACTTC[A/C]CCACCCTGTCTGTAC	79004
rs555902789	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425327	CCCTCTCTGTTCCCC[C/G]AAGTAGAACCATGCC	79004
rs556077135	snp	C/T	1.70026e-05	0.00291565	missense	CUEDC2	GRCh38.p7	10:102424790	ATGACCTCATCCAAG[C/T]CACTGCAGGAAGGGA	79004
rs556433185	snp	A/T	0.0310518	0.120672	intron-variant	CUEDC2	GRCh38.p7	10:102428085	TAACTGGGATTACAG[A/T]CATGTGCACCACACC	79004
rs557015029	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430867	AACATGATTTCCATG[A/G]GACATTTCAAATTCC	79004
rs557074049	snp	G/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431529	GGCAAGTTAATGGCA[G/T]ATTTACACCCAGGCT	79004
rs557135574	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423060	GAGCTGTAGGGAAAC[C/T]GAACTGTGAGGACCT	79004
rs557204783	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102423935	TAGGTAGGGGTTGGG[A/G]CTTAACACCAAGGTG	79004
rs557866465	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102427704	TCTCCCCACTCCATC[C/T]TCCCCCCAACAACCT	79004
rs558131590	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431284	AGCTGGGATTACAGT[C/T]GCATGCCACCATGCC	79004
rs558149486	snp	C/T	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102429955	AGGCGCCTGCCACAA[C/T]GCCCAGCTAATTTTT	79004
rs558287934	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433402	TCCTCCCATCTCAGC[C/T]TCTGGAGTAGCTGGA	79004
rs558383278	snp	A/T			intron-variant	CUEDC2	GRCh38.p7	10:102426521	TCTTTCACCCCTACC[A/T]GTCAATCACCAAGTC	79004
rs558486522	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432603	ACCAACGAGATCAAA[C/G]GCGGGGCCCAGAGCG	79004
rs558596412	snp	A/G			synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423465	TGGCTTGAGGTTGAT[A/G]TATGTGGCCTTCATC	79004
rs558605609	snp	C/T	1.67167e-05	0.00289103	missense	CUEDC2	GRCh38.p7	10:102424175	CCTCCTCAGCGCCAG[C/T]TGCCTAAGGGTACAA	79004
rs558774864	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431202	TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG	79004
rs558810832	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433553	TGTACCTTTTGCATT[C/T]CCTTAACAGCAATGT	79004
rs558905171	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426906	GGCTCAAAGCAGTTC[A/G]CCCACCTCAGCCTCC	79004
rs559245866	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434572	AGGAAGGGGCACATT[C/T]GCGTCGCTTTGCCCA	79004
rs559267272	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102429389	ACCTGGCTTGACTGC[A/G]GTAGTCAGATTTAAA	79004
rs559654701	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102426287	TTGGGAGTCAGGAGC[A/G]TATGGGTGGTAATGA	79004
rs560358910	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102429477	CAAGACTTTCAAGTG[G/T]GTTGGGACAGGGCTA	79004
rs560829969	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431028	TAGCATTTATTGCCT[C/T]TGCTTACGAGGCATT	79004
rs561012202	snp	G/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102430318	GGGATTACAAGCATG[G/T]GCCACCATGCTCGGC	79004
rs561106679	snp	C/T	3.33645e-05	0.00408425	intron-variant	CUEDC2	GRCh38.p7	10:102424261	ACCCTCCTCTACCAG[C/T]ACCTCATCTTGGGTG	79004
rs561168043	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102424920	ATCTTTAAGGCCAGA[C/G]AGTATAACCCCCTCC	79004
rs561569734	snp	G/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429207	ATTATTTGGACAATG[G/T]TTAATGTTTCTTCCA	79004
rs562484166	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102424210	TAACAAGAGGCAATA[C/T]TCCCCCCTTTCCAGC	79004
rs562706113	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102432358	CACATGACGAGGCAG[G/T]CCTGAGCAAACTGGA	79004
rs562833864	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434662	GACTTTGAACTCTGG[A/C]CGGGCAGGCCCCTAG	79004
rs562865002	snp	A/G	0.000100078	0.00707313	missense	CUEDC2	GRCh38.p7	10:102425130	CTGAGGTCGGCCTCC[A/G]GGAGGTGTGTCTGGA	79004
rs562971525	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434065	TTCCTCTCTCCTAGG[C/G]ACTAAGGCAGTGCCA	79004
rs563016316	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426330	CCATAGGTCCAAATG[C/T]CAGCTCATCATCCCA	79004
rs563102773	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429590	GAAGCCCCAGCCTAC[A/C]AGGGGAATTCATACC	79004
rs563575790	snp	C/T	0.00993419	0.0697739	intron-variant	CUEDC2	GRCh38.p7	10:102430181	TATTTATTTATTTTA[C/T]TTTTGAGACAGAGTT	79004
rs563869491	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431977	GGAGCTAGTGTGAAA[A/G]GAGTCCTAGCGAACT	79004
rs564403157	snp	C/T	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102427184	CTCTGGCCATTTCTT[C/T]GAAGGCCCTTTCTCT	79004
rs564973487	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431162	TATGTATTTTTGAGA[C/T]GGAGTCTCGCTCTGC	79004
rs565049079	in-del	-/TTTG			intron-variant	CUEDC2	GRCh38.p7	10:102427931	ACCCTGGCTTTGTTT[-/TTTG]TTTGTTTGTTTGTTT	79004
rs565280352	snp	C/G	0.000236167	0.0108641	intron-variant	CUEDC2	GRCh38.p7	10:102425099	GACATGAGCCTTCCG[C/G]GGGACCCGTCTCTAC	79004
rs565304864	snp	C/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102427677	TCTTGCCTGCAAGAA[C/G]TTCCTAACCCTTCTC	79004
rs565419011	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433865	TGGGGAAGCCCCACA[A/G]CCCTCCCCTCTTGGG	79004
rs565431863	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425914	GCTGAGCTTCCTCCT[A/G]TCTGTGTCCTGCGGG	79004
rs565442883	snp	G/T	0.00159617	0.0282053	intron-variant	CUEDC2	GRCh38.p7	10:102426798	ACCTACTAGTTTTTT[G/T]TTGTTGTTGTTTGTT	79004
rs565621309	snp	C/T	0.00318978	0.0398085	intron-variant	CUEDC2	GRCh38.p7	10:102428599	TTTAAAATTCCCTTC[C/T]TTGGCTGGGCACGGT	79004
rs565689522	snp	C/G	0.00159617	0.0282053	intron-variant	CUEDC2	GRCh38.p7	10:102428469	GTATGTATTGAGCAC[C/G]TAGCCAGCACGGGCA	79004
rs566108248	snp	A/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430407	CTCCCGACCTCAGGT[A/G]ATCTGCCCGCCTAGG	79004
rs566369214	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429891	ATGGTGTGAACCTGA[C/T]AGGGTCAAGCAATTC	79004
rs566587858	snp	C/G/T			intron-variant	CUEDC2	GRCh38.p7	10:102426290	GGAGTCAGGAGCATA[C/G/T]GGGTGGTAATGAATG	79004
rs567428969	snp	C/G	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430745	CATCCTTCCTGCTCA[C/G]GGGCTCCTAATACTT	79004
rs568063258	snp	A/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102427402	GGACATCTACCTCTC[A/T]AACACTGCCACGTGT	79004
rs568249003	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102426700	GCAGTGGTATGATCT[C/T]GGCTCACTGCAACCT	79004
rs568640397	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428715	ATATCAAGACCCCAT[A/C]TCTCTTTTTGTAGAA	79004
rs568930165	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102426741	AGCTCAAGCCATCCT[C/G]CTGCCTTAGCCTCCG	79004
rs569046994	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102432341	GCTGTGGCCTTGGAG[A/G]ACACATGACGAGGCA	79004
rs569068100	snp	A/C	0.00199481	0.0315187	intron-variant	CUEDC2	GRCh38.p7	10:102430403	CGAACTCCCGACCTC[A/C]GGTGATCTGCCCGCC	79004
rs569360918	snp	A/C	0.0023933	0.0345097	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433210	GATTACAGGCATGAG[A/C]CACCGCGCCTGGCCT	79004
rs569734879	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102428619	CTGGGCACGGTGCCT[C/T]ATGCCTGTAATTCCA	79004
rs570317332	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430538	GGTTTTTAGCCAAGG[C/T]CTGGGGGCCAGGGAA	79004
rs571705763	snp	C/T	0.00119737	0.0244387	intron-variant	CUEDC2	GRCh38.p7	10:102431435	AGGCATGAACCACCG[C/T]GCCCGGCCGTATTAT	79004
rs571802593	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425463	CCTCTCCCCACCCCC[A/C]TACCCCATTCCCCAG	79004
rs573167307	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423191	GGTTGGGGAGGAAAG[A/G]TCAGACAGGCATAGT	79004
rs573169242	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432567	TTGTCCCGCGCGGTG[C/T]AGCTCTCATCCCCCA	79004
rs573379772	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102427274	TTCTCACTGCAGCGC[G/T]CTCTCTCTCTCTGGA	79004
rs573414055	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434543	TGTTGGCTGCTTGGG[A/G]GAGGTAGCAGGGAAG	79004
rs573475796	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433633	CCTGGGATTTTGGAC[A/G]TGGTCTGGGAGAGGT	79004
rs573532973	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102429289	ACTCAGCATCTCTCA[C/T]GAAGTGGGCACTCAA	79004
rs573789758	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430012	ACCATGTTGGCCAGG[A/C]TGGTCTCGAACTCCT	79004
rs574059404	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102431364	GGCCAGACTGGTCTC[A/G]AACTCCTGACCTCAG	79004
rs574190843	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433558	CTTTTGCATTCCCTT[A/T]ACAGCAATGTCTCCC	79004
rs574347732	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102425425	CTAGAGGAGGCGCCC[C/T]CCCACCTCTCCCCAC	79004
rs574459384	snp	A/T	0.00199481	0.0315187	intron-variant	CUEDC2	GRCh38.p7	10:102424859	CACCCCCACCTATCC[A/T]GAGACTCCAGCCCTC	79004
rs574474991	snp	A/G	0.00199481	0.0315187	intron-variant	CUEDC2	GRCh38.p7	10:102426983	ATTTCTTAGACTGAG[A/G]TCATCAGTTACTTTT	79004
rs574770524	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426358	CCACTCAGAAGGCTC[C/T]GAGGCACCACCAGTT	79004
rs575219527	snp	C/G	0.0310518	0.120672	intron-variant	CUEDC2	GRCh38.p7	10:102428086	AACTGGGATTACAGA[C/G]ATGTGCACCACACCT	79004
rs575288983	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102428305	GTAGTATACCCTCTG[A/G]GCCTTCTGCCTCATC	79004
rs575318372	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423092	TGGTGAGAGGCCAGT[A/G]CCCTGCCCCACCCTG	79004
rs575331676	in-del	-/GCCCA	0.00021575	0.010384	intron-variant	CUEDC2	GRCh38.p7	10:102423771	GGAAGACCCTCTAGG[-/GCCCA]GCCCAGCCCAGCCCA	79004
rs575426621	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102431434	CAGGCATGAACCACC[A/G]CGCCCGGCCGTATTA	79004
rs575464139	snp	A/C			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433917	GGGAAGAGTCCCCTT[A/C]AAGGATAAAATTTCC	79004
rs575467972	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432735	GACGGGCTCCCTTGG[C/T]GGCCAGTTTTGTTGC	79004
rs575620443	snp	C/T	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102431627	CCCCATCCTATATTC[C/T]GAATCTCCTCTCCTG	79004
rs576284114	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102432182	ATCCCTGCATCCAAA[A/G]TCAGGCGGGAGCACA	79004
rs576799447	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433428	CTGGAACCACAGGCG[C/T]GTGCCACCACGCCGA	79004
rs577394650	snp	A/G	0.000798403	0.0199641	intron-variant	CUEDC2	GRCh38.p7	10:102426934	TCCCAAAGTGCTGGG[A/G]TTACAGCCATGAGTC	79004
rs577467403	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434586	TCGCGTCGCTTTGCC[C/G]ATAAAAACACTGCCA	79004
rs577479424	snp	C/T	0.00279162	0.0372561	intron-variant	CUEDC2	GRCh38.p7	10:102425926	CCTGTCTGTGTCCTG[C/T]GGGACATCCATGGCT	79004
rs577789307	snp	A/C	0.000399281	0.0141238	intron-variant	CUEDC2	GRCh38.p7	10:102430802	AAGATCTGGTCTGCC[A/C]GACTGGTTTCCTAAG	79004
rs745317739	snp	C/T	3.31972e-05	0.004074	missense	CUEDC2	GRCh38.p7	10:102424667	GGGATGTGGGCGAAG[C/T]CAGGCACATAGGCCT	79004
rs745535548	snp	A/G	1.70697e-05	0.00292139	intron-variant	CUEDC2	GRCh38.p7	10:102424802	AAGCCACTGCAGGAA[A/G]GGAACAGGACAAGCC	79004
rs745555678	snp	A/G	1.65608e-05	0.00287752	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423437	TGCCTCAATGGAAGC[A/G]GTACTTTCTGGCTGG	79004
rs745603729	snp	G/T	5.01207e-05	0.00500578	missense	CUEDC2	GRCh38.p7	10:102424027	CAGGCTGCAGGCCCC[G/T]CTTCCTTTCCCTCTA	79004
rs745610763	in-del	-/TTAT			intron-variant	CUEDC2	GRCh38.p7	10:102430156	TTTAATTTTATTTAT[-/TTAT]TTATTTATTTATTTA	79004
rs745918882	snp	C/G	1.65674e-05	0.00287809	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422916	GTGGACATCGACGTG[C/G]AGCCGCCGCTGCACC	79004
rs745973349	snp	C/G	1.66043e-05	0.00288129	intron-variant	CUEDC2	GRCh38.p7	10:102424481	GAATCACTCAGGTGC[C/G]CAGAGCCCCAGACTC	79004
rs745998780	snp	C/T	1.95322e-05	0.00312502	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422819	GACATTGGCCGAGTA[C/T]TGCCCCGTGCTGCGT	79004
rs746151781	snp	G/T	1.65806e-05	0.00287924	missense	CUEDC2	GRCh38.p7	10:102424314	ACCTAGTCTCTTCTT[G/T]GAGCATTTCGGGCCG	79004
rs746309186	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429571	CTTTGGAAAGCAGGA[C/T]TGAGAAGCCCCAGCC	79004
rs746408201	snp	A/C	4.97409e-05	0.00498678	intron-variant	CUEDC2	GRCh38.p7	10:102424402	CAGGTTCTCTTAAAG[A/C]GGCAAAGAGAGCATC	79004
rs746573861	snp	C/T	1.67368e-05	0.00289277	synonymous-codon	CUEDC2	GRCh38.p7	10:102424017	GGGGCCCTCCCAGGC[C/T]GCAGGCCCCTCTTCC	79004
rs746698075	snp	A/G	1.65999e-05	0.00288091	synonymous-codon	CUEDC2	GRCh38.p7	10:102424515	TTTGTTCCTGGCATC[A/G]CTCAGCTGCCCTGAG	79004
rs746980427	snp	C/G	1.69671e-05	0.00291261	intron-variant	CUEDC2	GRCh38.p7	10:102423879	AGAGAGGGGAGGCCT[C/G]GTCTAGGCCCAAGGG	79004
rs747371833	snp	A/G	1.656e-05	0.00287745	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423546	CACTACCTGGTTGTC[A/G]ATGTATCGGATCAGC	79004
rs747575180	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428353	AGCTGCCATTTGGAC[C/T]TATGGGTCTGGAGCC	79004
rs747651878	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102429489	GTGGGTTGGGACAGG[C/G]CTACCTTCTATGCTT	79004
rs747653979	snp	A/G	1.65726e-05	0.00287855	intron-variant	CUEDC2	GRCh38.p7	10:102423741	AACTGGCTGGGTGAA[A/G]CTCCTGTCACCCTGG	79004
rs748112098	snp	C/T	1.65847e-05	0.0028796	intron-variant	CUEDC2	GRCh38.p7	10:102424414	AAGAGGCAAAGAGAG[C/T]ATCAGGTTTGCCAAG	79004
rs748337692	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431894	GTAAGAAGTACTATG[C/T]TGCTCCCTTGGGGTG	79004
rs748506038	snp	A/C/T	0.000331759	0.0128759	missense	CUEDC2	GRCh38.p7	10:102424650	TAGCCAGAACCTACC[A/C/T]GGGGATGTGGGCGAA	79004
rs748556574	snp	C/T	3.34091e-05	0.00408698	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422963	GCAGGATATGGCGGG[C/T]TTCGCACCTTTTGTC	79004
rs748745973	snp	A/G	1.65608e-05	0.00287752	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423578	TCTTGGGGGCCTGTC[A/G]GGCAATCAGCAGTGA	79004
rs748773100	snp	C/G	5.02037e-05	0.00500993	synonymous-codon	CUEDC2	GRCh38.p7	10:102425117	GACCCGTCTCTACCT[C/G]AGGTCGGCCTCCGGG	79004
rs748849187	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102426624	GCTCCAAAATCTCCA[C/G]CAAAATTTCTTCTTT	79004
rs748872838	snp	C/G	3.44003e-05	0.00414716	intron-variant	CUEDC2	GRCh38.p7	10:102424816	AGGGAACAGGACAAG[C/G]CCTGGGTAGGACACT	79004
rs748939078	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102427962	TTTTGTTTTGTTTTT[A/G]AGACAGCCTCACTCT	79004
rs748976973	snp	A/G	1.65641e-05	0.00287781	intron-variant	CUEDC2	GRCh38.p7	10:102423720	CACCATCATGTACCT[A/G]TCAAAAACTGGCTGG	79004
rs749145931	snp	C/T	1.67307e-05	0.00289224	intron-variant	CUEDC2	GRCh38.p7	10:102424195	TAAGGGTACAAACGT[C/T]AACAAGAGGCAATAC	79004
rs749421817	snp	C/T	3.31334e-05	0.00407009	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423415	GGCTCGGGCAGAGTC[C/T]GGCGAGTGCCTCAAT	79004
rs749490513	snp	C/T	1.66796e-05	0.00288782	missense	CUEDC2	GRCh38.p7	10:102424061	GCATCTGCACAGCTT[C/T]TTCCAAGTCCCCCCG	79004
rs749494722	in-del	-/A	1.65652e-05	0.0028779	intron-variant	CUEDC2	GRCh38.p7	10:102423723	CATCATGTACCTGTC[-/A]AAAACTGGCTGGGTG	79004
rs749548368	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430242	GGCGCGATCTTGGCT[C/T]ACCGCAACCTCCACC	79004
rs749599580	snp	G/T	1.6604e-05	0.00288127	missense	CUEDC2	GRCh38.p7	10:102424503	CCCAGACTCACCTTT[G/T]TTCCTGGCATCGCTC	79004
rs749716360	snp	A/C	1.65822e-05	0.00287938	intron-variant	CUEDC2	GRCh38.p7	10:102424418	GGCAAAGAGAGCATC[A/C]GGTTTGCCAAGGCTC	79004
rs749716884	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102431500	GAGGTTAAGTAACTT[G/T]CCCAAGGTCACAAGG	79004
rs749829555	snp	C/G	3.91811e-05	0.00442595	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422951	CCTGGTGCTGCTGCA[C/G]GATATGGCGGGCTTC	79004
rs750365110	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429155	TCTATGCAGGCTGCA[A/G]GTTTTCTGACTAGCA	79004
rs750386906	snp	A/G	1.67189e-05	0.00289122	intron-variant	CUEDC2	GRCh38.p7	10:102424184	CGCCAGTTGCCTAAG[A/G]GTACAAACGTTAACA	79004
rs750486565	snp	C/T	1.6582e-05	0.00287936	intron-variant	CUEDC2	GRCh38.p7	10:102424602	TGACTCTGCCCACCC[C/T]ATAATCAGCCAGCCC	79004
rs750565558	snp	C/G	1.656e-05	0.00287745	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423493	ATCTCCTCGGCCTCA[C/G]GGTTCCGCACATCTT	79004
rs750651141	snp	A/G	3.3315e-05	0.00408122	synonymous-codon	CUEDC2	GRCh38.p7	10:102424711	GAAAGCCTCCATATC[A/G]AAGTTCTCCTCTGAT	79004
rs750743278	snp	C/T	1.66905e-05	0.00288876	missense	CUEDC2	GRCh38.p7	10:102424106	CCCACTGGGCCTGCT[C/T]CACCGAACAGGTAGG	79004
rs750959978	in-del	-/ACAG	1.66824e-05	0.00288806	intron-variant	CUEDC2	GRCh38.p7	10:102425209	CTCTTCTGAAGGGAC[-/ACAG]ACAGGATGGCCAGGC	79004
rs750989200	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431222	TCAGCTCACTGCAAC[C/T]TCCACCTCCCTGGTT	79004
rs751195214	in-del	-/AAAAAA			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434376	CAAGACCCTGTCTCA[-/AAAAAA]AAAAAAAAAAAAAAA	79004
rs751216172	snp	C/T	3.34526e-05	0.00408965	intron-variant	CUEDC2	GRCh38.p7	10:102424245	TGGGTCCCTCATCGG[C/T]ACCCTCCTCTACCAG	79004
rs751395271	snp	A/G	1.72815e-05	0.00293946	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423016	GCCAATCGGAGCACA[A/G]CTGGACTGTGTGGCT	79004
rs751445853	snp	A/C/G			intron-variant	CUEDC2	GRCh38.p7	10:102426144	GGTGGGGATGAGGGG[A/C/G]ACACTCTGTCTTATT	79004
rs751938662	snp	A/G	1.65605e-05	0.0028775	synonymous-codon	CUEDC2	GRCh38.p7	10:102423699	CTTCTGATCCTCTGC[A/G]CTATCCACCATCATG	79004
rs752010575	snp	G/T	1.66599e-05	0.00288611	missense	CUEDC2	GRCh38.p7	10:102423820	GGATGAAGGACTTCA[G/T]CTCATCCTTTTGGGG	79004
rs752291896	snp	C/T	1.70662e-05	0.00292109	intron-variant	CUEDC2	GRCh38.p7	10:102425239	AGGCCTTCTTCTGCC[C/T]GCCCCCACCCACTGG	79004
rs752297247	snp	C/G	3.36061e-05	0.00409901	synonymous-codon	CUEDC2	GRCh38.p7	10:102424005	AGATACCTGGTTGGG[C/G]CCCTCCCAGGCTGCA	79004
rs752303556	snp	A/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432678	AGTTGCCCACAACAG[A/G]GCGGAGCTCCTGCTC	79004
rs752346792	snp	C/T	1.67158e-05	0.00289096	missense	CUEDC2	GRCh38.p7	10:102424169	GAAGCTCCTCCTCAG[C/T]GCCAGTTGCCTAAGG	79004
rs752383453	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431035	TATTGCCTCTGCTTA[C/T]GAGGCATTGTCCTAA	79004
rs752429940	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432730	CTATGGACGGGCTCC[C/T]TTGGCGGCCAGTTTT	79004
rs752545368	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428623	GCACGGTGCCTCATG[C/T]CTGTAATTCCAGCAC	79004
rs752694284	snp	A/G	4.4829e-05	0.00473418	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422890	GCCTGAGCCGCTTGC[A/G]GAAGCGCGGCGTGGA	79004
rs753151719	snp	C/G	5.05821e-05	0.00502877	intron-variant	CUEDC2	GRCh38.p7	10:102425100	ACATGAGCCTTCCGG[C/G]GGACCCGTCTCTACC	79004
rs753209808	snp	C/T	1.656e-05	0.00287745	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423531	CTCCCCTTTGGTGCT[C/T]ACTACCTGGTTGTCG	79004
rs753564983	snp	G/T	6.66756e-05	0.0057735	missense	CUEDC2	GRCh38.p7	10:102424270	TACCAGTACCTCATC[G/T]TGGGTGTCTGCAGCA	79004
rs753723179	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428010	GCAGTGGTGCCATCT[C/T]GGCTCACTGCAACCT	79004
rs753821757	snp	A/G	1.65729e-05	0.00287857	synonymous-codon	CUEDC2	GRCh38.p7	10:102424366	GGGCACCTGACCTTG[A/G]ACACCAGAGCTCTGC	79004
rs753914938	snp	A/G	3.31192e-05	0.00406921	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423500	CGGCCTCAGGGTTCC[A/G]CACATCTTTGAATCG	79004
rs753968673	snp	A/G	1.67542e-05	0.00289427	synonymous-codon	CUEDC2	GRCh38.p7	10:102424744	GCCCGAGGGGCCCAG[A/G]TCCTCCAGGACCCCA	79004
rs754073677	snp	A/C	1.656e-05	0.00287745	synonymous-codon	CUEDC2	GRCh38.p7	10:102423666	TCTCACCTCCTTGGG[A/C]GCCATGGGCCGGTGA	79004
rs754098486	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425794	CTTTCCATCCTCCTC[C/T]CCAAGGCCTGAGGAG	79004
rs754110039	in-del	-/TTTT/TTTTTTTT			intron-variant	CUEDC2	GRCh38.p7	10:102430151	TTTTTTTTAATTTTA[-/TTTT/TTTTTTTT]TTTATTTATTTATTT	79004
rs754375845	snp	C/T	1.65847e-05	0.0028796	intron-variant	CUEDC2	GRCh38.p7	10:102424639	CCTCCTGGCCCTAGC[C/T]AGAACCTACCTGGGG	79004
rs754464350	snp	G/T	5.0816e-05	0.00504038	intron-variant	CUEDC2	GRCh38.p7	10:102425229	CAGGATGGCCAGGCC[G/T]TCTTCTGCCTGCCCC	79004
rs754492363	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428015	GGTGCCATCTTGGCT[C/T]ACTGCAACCTCTGCC	79004
rs754577010	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429415	TTAAATCCAGGTCAC[C/T]TAGTTCAGCATCTAT	79004
rs754819464	snp	A/G	6.66411e-05	0.00577201	synonymous-codon	CUEDC2	GRCh38.p7	10:102424273	CAGTACCTCATCTTG[A/G]GTGTCTGCAGCAGCA	79004
rs754851509	snp	G/T	0.000142161	0.00842971	intron-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422761	TACCCCACCAAAGGT[G/T]TGGTGGCCTCATGTC	79004
rs755109440	snp	A/G	1.656e-05	0.00287745	stop-gained, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423515	GCACATCTTTGAATC[A/G]CTCCCCTTTGGTGCT	79004
rs755287238	snp	A/T	1.6585e-05	0.00287962	intron-variant	CUEDC2	GRCh38.p7	10:102424640	CTCCTGGCCCTAGCC[A/T]GAACCTACCTGGGGA	79004
rs755305938	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433275	TCCCTCCCTCCCTTC[C/T]TTCCTTCTCTTTCTT	79004
rs755450757	snp	A/G	3.31312e-05	0.00406995	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423416	GCTCGGGCAGAGTCC[A/G]GCGAGTGCCTCAATG	79004
rs755483104	snp	A/G	1.68542e-05	0.0029029	synonymous-codon	CUEDC2	GRCh38.p7	10:102424771	CCCAAGCACATAGGA[A/G]AAGATGACCTCATCC	79004
rs755875589	snp	A/G	1.71496e-05	0.00292822	intron-variant	CUEDC2	GRCh38.p7	10:102424810	GCAGGAAGGGAACAG[A/G]ACAAGCCCTGGGTAG	79004
rs755971002	snp	C/G	3.33667e-05	0.00408439	intron-variant	CUEDC2	GRCh38.p7	10:102424260	TACCCTCCTCTACCA[C/G]TACCTCATCTTGGGT	79004
rs755974018	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429279	ACCAGTGTATACTCA[A/G]CATCTCTCATGAAGT	79004
rs756104194	snp	C/T	1.65707e-05	0.00287838	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423403	CTGAGCCTAGAAGGC[C/T]CGGGCAGAGTCCGGC	79004
rs756192745	in-del	-/CCTAG	2.698e-05	0.00367277	intron-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422777	TGGTGGCCTCATGTC[-/CCTAG]CCTCACCCTGCTCCT	79004
rs756196969	snp	C/T	1.65817e-05	0.00287933	intron-variant	CUEDC2	GRCh38.p7	10:102424616	CCATAATCAGCCAGC[C/T]CCTTCCTCCTCCTGG	79004
rs756228671	snp	C/G	2.42774e-05	0.00348398	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422921	CATCGACGTGGAGCC[C/G]CCGCTGCACCAGGCC	79004
rs756262802	in-del	-/CT	3.31631e-05	0.00407191	intron-variant	CUEDC2	GRCh38.p7	10:102424590	GCAGTGAGAGGATGA[-/CT]CTGCCCACCCCATAA	79004
rs756406865	snp	A/G	1.66818e-05	0.00288802	synonymous-codon	CUEDC2	GRCh38.p7	10:102424122	CACCGAACAGGTAGG[A/G]AACACCTCCAGGAGT	79004
rs756607690	snp	C/T	1.66043e-05	0.00288129	intron-variant	CUEDC2	GRCh38.p7	10:102424482	AATCACTCAGGTGCC[C/T]AGAGCCCCAGACTCA	79004
rs756608206	snp	A/G	1.6884e-05	0.00290547	splice-donor-variant	CUEDC2	GRCh38.p7	10:102423994	GTGCTGGGAAAAGAT[A/G]CCTGGTTGGGGCCCT	79004
rs756772425	snp	C/T	1.67206e-05	0.00289137	missense	CUEDC2	GRCh38.p7	10:102424178	CCTCAGCGCCAGTTG[C/T]CTAAGGGTACAAACG	79004
rs756800478	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432863	CCGAAACCTTTCTCT[C/T]TCTTTCTCTCTCTCT	79004
rs757090976	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102427193	TTTCTTCGAAGGCCC[C/T]TTCTCTGTCCCCTTC	79004
rs757094048	in-del	-/A			intron-variant	CUEDC2	GRCh38.p7	10:102426234	CTGTTGACATGCTCC[-/A]ATTCCCATCTACATG	79004
rs757129436	snp	G/T	0.000374181	0.013673	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423024	GAGCACAGCTGGACT[G/T]TGTGGCTGGGGCCTG	79004
rs757162456	in-del	-/CAGGCTGGAGTG			intron-variant	CUEDC2	GRCh38.p7	10:102429862	TTCGCTCTTGTTGCC[-/CAGGCTGGAGTG]CAATGGTGTGAACCT	79004
rs757181226	snp	A/G	1.67203e-05	0.00289134	missense	CUEDC2	GRCh38.p7	10:102424021	CCCTCCCAGGCTGCA[A/G]GCCCCTCTTCCTTTC	79004
rs757231853	snp	A/C	1.6604e-05	0.00288127	intron-variant	CUEDC2	GRCh38.p7	10:102424474	GGATTATGAATCACT[A/C]AGGTGCCCAGAGCCC	79004
rs757360529	snp	C/T	1.65781e-05	0.00287902	missense	CUEDC2	GRCh38.p7	10:102424392	TCTGCGGTTGCAGGT[C/T]CTCTTAAAGAGGCAA	79004
rs757521199	snp	C/T	2.38883e-05	0.00345595	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422908	AGCGCGGCGTGGACA[C/T]CGACGTGGAGCCGCC	79004
rs757705358	snp	C/T	1.65605e-05	0.0028775	missense	CUEDC2	GRCh38.p7	10:102423700	TTCTGATCCTCTGCG[C/T]TATCCACCATCATGT	79004
rs757848965	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431091	TAATCCTTACAATAA[C/T]TCTAAAATGTAGATA	79004
rs757863273	snp	A/G	1.69223e-05	0.00290876	intron-variant	CUEDC2	GRCh38.p7	10:102423872	GTCCTGCAGAGAGGG[A/G]AGGCCTGGTCTAGGC	79004
rs757886181	snp	C/T	3.35599e-05	0.00409619	synonymous-codon	CUEDC2	GRCh38.p7	10:102424008	TACCTGGTTGGGGCC[C/T]TCCCAGGCTGCAGGC	79004
rs757904459	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429516	GCTTACAGTTGCCTG[A/G]TCCCGAGTGGTAACA	79004
rs757973601	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102429148	TACACTCTCTATGCA[G/T]GCTGCAAGTTTTCTG	79004
rs758194561	in-del	-/AAAAAAA			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434375	GCAAGACCCTGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA	79004
rs758226382	snp	C/T	2.30083e-05	0.0033917	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422897	CCGCTTGCGGAAGCG[C/T]GGCGTGGACATCGAC	79004
rs758326693	snp	C/T	2.0798e-05	0.00322468	intron-variant	CUEDC2, FBXL15	GRCh38.p7	10:102422801	ACCCTGCTCCTCCCT[C/T]AGGACATTGGCCGAG	79004
rs758328685	snp	C/T	4.9807e-05	0.00499009	intron-variant	CUEDC2	GRCh38.p7	10:102424457	AGGCAGTTGGGGGAG[C/T]GGGATTATGAATCAC	79004
rs758521543	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425965	CACTCCTCAGGGCTC[C/T]GCTCAAATGTTACCT	79004
rs758652096	snp	C/T	3.31203e-05	0.00406928	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423536	CTTTGGTGCTCACTA[C/T]CTGGTTGTCGATGTA	79004
rs758737648	snp	A/C	1.68286e-05	0.0029007	intron-variant	CUEDC2	GRCh38.p7	10:102425104	GAGCCTTCCGGGGGA[A/C]CCGTCTCTACCTGAG	79004
rs758905502	snp	C/G	3.31203e-05	0.00406928	missense	CUEDC2	GRCh38.p7	10:102423693	GTGAATCTTCTGATC[C/G]TCTGCGCTATCCACC	79004
rs758914812	snp	G/T	9.62232e-05	0.00693559	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422984	ACCTTTTGTCAACCT[G/T]CAGGTCTGACCCGCC	79004
rs758937762	in-del	-/GATGAGGGCAGTGAGAG	1.65853e-05	0.00287964	intron-variant	CUEDC2	GRCh38.p7	10:102424567	TTGTGCCCCTGAAAA[-/GATGAGGGCAGTGAGAG]GATGAGGGCAGTGAG	79004
rs759187478	snp	G/T	1.65908e-05	0.00288012	missense	CUEDC2	GRCh38.p7	10:102424545	GAGCTTCTGCATCAT[G/T]TCCCCTATTGTGCCC	79004
rs759524051	snp	A/G/T	8.29778e-05	0.00644072	intron-variant	CUEDC2	GRCh38.p7	10:102424454	AGCAGGCAGTTGGGG[A/G/T]AGCGGGATTATGAAT	79004
rs759545898	snp	C/T	4.96792e-05	0.00498368	missense	CUEDC2	GRCh38.p7	10:102423671	CCTCCTTGGGAGCCA[C/T]GGGCCGGTGAATCTT	79004
rs759596094	snp	A/G	1.66366e-05	0.0028841	synonymous-codon	CUEDC2	GRCh38.p7	10:102425182	TGACGATCCTCTCCA[A/G]CTCCATGCTCTCTCT	79004
rs759596414	snp	A/G	0.00013511	0.00821808	intron-variant	CUEDC2	GRCh38.p7	10:102425098	TGACATGAGCCTTCC[A/G]GGGGACCCGTCTCTA	79004
rs759620867	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425852	TCCAGCCTCCCCAGT[C/T]CCTCCTCCCTAGCTT	79004
rs759778636	snp	C/G	1.66114e-05	0.00288192	intron-variant	CUEDC2	GRCh38.p7	10:102423773	AAGACCCTCTAGGGC[C/G]CAGCCCAGCCCAGCC	79004
rs759834371	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102426928	TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGCCA	79004
rs760001952	snp	C/T	6.69949e-05	0.00578731	intron-variant	CUEDC2	GRCh38.p7	10:102424242	CCCTGGGTCCCTCAT[C/T]GGTACCCTCCTCTAC	79004
rs760040013	snp	C/T	1.65828e-05	0.00287943	intron-variant	CUEDC2	GRCh38.p7	10:102424431	TCAGGTTTGCCAAGG[C/T]TCTGGGGAGCAGGCA	79004
rs760292513	snp	C/T	1.65718e-05	0.00287848	missense	CUEDC2	GRCh38.p7	10:102424341	GCCGCTGCAGGGGCT[C/T]TGGGGAGATGGGCAC	79004
rs760347079	snp	C/G	2.00588e-05	0.00316686	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422859	GTGCGGCACTGCCAC[C/G]ATGTGGCGGAGTCCA	79004
rs760461972	snp	C/T	1.65762e-05	0.00287886	intron-variant	CUEDC2	GRCh38.p7	10:102423749	GGGTGAAGCTCCTGT[C/T]ACCCTGGGAAGACCC	79004
rs760637584	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102432122	TTGTCCTCTGATACC[C/T]AAGTCAGACCTTAGA	79004
rs760646761	in-del	-/CTC	1.66952e-05	0.00288917	cds-indel	CUEDC2	GRCh38.p7	10:102424158	CACCCCTGGCAGAAG[-/CTC]CTCCTCAGCGCCAGT	79004
rs760866177	snp	C/G	1.69723e-05	0.00291305	intron-variant	CUEDC2	GRCh38.p7	10:102425091	CCAGCACTGACATGA[C/G]CCTTCCGGGGGACCC	79004
rs760931357	snp	A/G	3.31197e-05	0.00406925	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423494	TCTCCTCGGCCTCAG[A/G]GTTCCGCACATCTTT	79004
rs761024451	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426794	CACCACCTACTAGTT[C/T]TTTGTTGTTGTTGTT	79004
rs761163255	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102425338	CCCCCAAGTAGAACC[A/C]TGCCCCCTCCTCCGC	79004
rs761272998	snp	C/T	1.67172e-05	0.00289108	intron-variant	CUEDC2	GRCh38.p7	10:102424249	TCCCTCATCGGTACC[C/T]TCCTCTACCAGTACC	79004
rs761445800	snp	C/T	6.62394e-05	0.00575459	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423485	TGGCCTTCATCTCCT[C/T]GGCCTCAGGGTTCCG	79004
rs761829591	snp	C/T	8.28041e-05	0.00643391	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423627	CAGTCCCACCCATTC[C/T]GCATCCCCAGCAACC	79004
rs761917378	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102429109	ATCACCCCTGACCTA[C/G]AACTCATTTGGGCCC	79004
rs762064469	snp	C/T	8.29098e-05	0.00643801	intron-variant	CUEDC2	GRCh38.p7	10:102424591	CAGTGAGAGGATGAC[C/T]CTGCCCACCCCATAA	79004
rs762253928	in-del	-/T	1.69447e-05	0.00291068	intron-variant	CUEDC2	GRCh38.p7	10:102425094	GCACTGACATGAGCC[-/T]TCCGGGGGACCCGTC	79004
rs762334456	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425264	CACTGGGCCTGGGGG[C/T]AGTGGCTCCTCCCTC	79004
rs762482935	in-del	-/AAAAA			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102434381	CCTGTCTCAAAAAAA[-/AAAAA]AAAAAAAAAAAAAAA	79004
rs762618761	snp	A/C	1.65603e-05	0.00287747	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423478	ATGTATGTGGCCTTC[A/C]TCTCCTCGGCCTCAG	79004
rs762792926	snp	A/G	1.65853e-05	0.00287964	intron-variant	CUEDC2	GRCh38.p7	10:102424564	CCTATTGTGCCCCTG[A/G]AAAGATGAGGGCAGT	79004
rs762845322	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432790	GGTCTTGAGAGGGGG[C/T]GGAGTCGAAGTGGGT	79004
rs762999951	snp	C/T	1.66203e-05	0.00288268	splice-donor-variant	CUEDC2	GRCh38.p7	10:102423797	CCCAGCCCAGACTCA[C/T]TTCTGCAGGATGAAG	79004
rs763019139	snp	C/G	0.000102401	0.00715473	intron-variant	CUEDC2	GRCh38.p7	10:102423947	GGGGCTTAACACCAA[C/G]GTGGAATGTAGCTGA	79004
rs763241118	snp	C/T	1.9204e-05	0.00309865	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422836	GCCCCGTGCTGCGTT[C/T]GCTGCGGGTGCGGCA	79004
rs763333548	snp	A/G	5.00396e-05	0.00500173	intron-variant	CUEDC2	GRCh38.p7	10:102425206	TCTCTCTTCTGAAGG[A/G]ACACAGACAGGATGG	79004
rs763594007	snp	A/G	3.34734e-05	0.00409091	intron-variant	CUEDC2	GRCh38.p7	10:102424243	CCTGGGTCCCTCATC[A/G]GTACCCTCCTCTACC	79004
rs763728203	snp	G/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432753	CCAGTTTTGTTGCGC[G/T]TAGGGAGGCGTTAGG	79004
rs763849130	snp	A/C	1.67167e-05	0.00289103	synonymous-codon	CUEDC2	GRCh38.p7	10:102424173	CTCCTCCTCAGCGCC[A/C]GTTGCCTAAGGGTAC	79004
rs763967766	snp	A/C/G	4.97453e-05	0.00498704	intron-variant	CUEDC2	GRCh38.p7	10:102424580	AAAGATGAGGGCAGT[A/C/G]AGAGGATGACTCTGC	79004
rs764002811	snp	A/G	9.41974e-05	0.0068622	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422903	GCGGAAGCGCGGCGT[A/G]GACATCGACGTGGAG	79004
rs764106858	snp	C/T	1.65603e-05	0.00287747	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423480	GTATGTGGCCTTCAT[C/T]TCCTCGGCCTCAGGG	79004
rs764109458	snp	A/G	1.70729e-05	0.00292167	intron-variant	CUEDC2	GRCh38.p7	10:102423948	GGGCTTAACACCAAG[A/G]TGGAATGTAGCTGAG	79004
rs764166470	snp	C/T	0.000158316	0.00889566	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102423012	GCCTGCCAATCGGAG[C/T]ACAGCTGGACTGTGT	79004
rs764528176	snp	C/T	1.68131e-05	0.00289935	intron-variant	CUEDC2	GRCh38.p7	10:102425106	GCCTTCCGGGGGACC[C/T]GTCTCTACCTGAGGT	79004
rs764713681	in-del	-/TT			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433450	CCACGCCGAGCTAAT[-/TT]TTTTTTTTTTTTTTT	79004
rs764809246	snp	C/T	0.000101921	0.00713794	downstream-variant-500B, stop-gained	CUEDC2, FBXL15	GRCh38.p7	10:102422985	CCTTTTGTCAACCTG[C/T]AGGTCTGACCCGCCT	79004
rs764849294	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102431025	TATTAGCATTTATTG[C/T]CTCTGCTTACGAGGC	79004
rs764890783	snp	C/T	3.37069e-05	0.00410516	missense	CUEDC2	GRCh38.p7	10:102423997	CTGGGAAAAGATACC[C/T]GGTTGGGGCCCTCCC	79004
rs764940689	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428617	GGCTGGGCACGGTGC[C/T]TCATGCCTGTAATTC	79004
rs765014235	snp	C/T			utr-variant-5-prime	CUEDC2	GRCh38.p7	10:102432620	CGGGGCCCAGAGCGG[C/T]TCCCTTCCAGAGGCG	79004
rs765074824	snp	A/T	2.19783e-05	0.00331491	downstream-variant-500B, stop-gained	CUEDC2, FBXL15	GRCh38.p7	10:102422887	CCAGCCTGAGCCGCT[A/T]GCGGAAGCGCGGCGT	79004
rs765147212	snp	C/G/T	4.97222e-05	0.00498589	missense	CUEDC2	GRCh38.p7	10:102424370	ACCTGACCTTGGACA[C/G/T]CAGAGCTCTGCGGTT	79004
rs765333986	snp	A/G	1.656e-05	0.00287745	synonymous-codon	CUEDC2	GRCh38.p7	10:102423672	CTCCTTGGGAGCCAT[A/G]GGCCGGTGAATCTTC	79004
rs765431246	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425935	GTCCTGCGGGACATC[C/T]ATGGCTCGTCCAGTC	79004
rs765459271	in-del	-/TTT			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433449	ACCACGCCGAGCTAA[-/TTT]TTTTTTTTTTTTTTT	79004
rs765481746	snp	A/C	3.32082e-05	0.00407468	intron-variant	CUEDC2	GRCh38.p7	10:102423780	TCTAGGGCCCAGCCC[A/C]GCCCAGCCCAGACTC	79004
rs766097598	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102429331	ACCCCAATTTACCTA[G/T]GAAGAAATGAAGTTC	79004
rs766107119	snp	C/T	8.07967e-05	0.00635545	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422861	GCGGCACTGCCACCA[C/T]GTGGCGGAGTCCAGC	79004
rs766172061	snp	C/G	4.97179e-05	0.00498562	missense	CUEDC2	GRCh38.p7	10:102424361	GAGATGGGCACCTGA[C/G]CTTGGACACCAGAGC	79004
rs766187713	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430757	TCAGGGGCTCCTAAT[A/G]CTTCTCCCCGCATAG	79004
rs766365536	snp	A/G	1.70516e-05	0.00291985	intron-variant	CUEDC2	GRCh38.p7	10:102423969	TGTAGCTGAGGCTAC[A/G]TGGTAGAGGGTGCTG	79004
rs766470053	snp	A/G	1.67284e-05	0.00289205	synonymous-codon	CUEDC2	GRCh38.p7	10:102424735	CTCTGATGGGCCCGA[A/G]GGGCCCAGGTCCTCC	79004
rs766578679	snp	C/T	1.656e-05	0.00287745	missense	CUEDC2	GRCh38.p7	10:102423659	TTAACTCTCTCACCT[C/T]CTTGGGAGCCATGGG	79004
rs766629598	snp	A/C	5.08893e-05	0.00504401	intron-variant	CUEDC2	GRCh38.p7	10:102425092	CAGCACTGACATGAG[A/C]CTTCCGGGGGACCCG	79004
rs766650842	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102425655	ACCCAGAACAGGCCA[C/T]CCACCCTCTGCACAA	79004
rs767032550	snp	A/T	1.67005e-05	0.00288963	intron-variant	CUEDC2	GRCh38.p7	10:102424256	TCGGTACCCTCCTCT[A/T]CCAGTACCTCATCTT	79004
rs767399993	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102429144	ATATTACACTCTCTA[C/T]GCAGGCTGCAAGTTT	79004
rs767573620	snp	C/T	1.65723e-05	0.00287852	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423395	TCTGGGATCTGAGCC[C/T]AGAAGGCTCGGGCAG	79004
rs767634234	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430590	TCCCCAAATAAAAAG[A/G]CTTGCTCCCCTAAGC	79004
rs767718515	snp	C/T	3.33139e-05	0.00408116	missense	CUEDC2	GRCh38.p7	10:102424710	TGAAAGCCTCCATAT[C/T]GAAGTTCTCCTCTGA	79004
rs767805099	in-del	-/C	1.66938e-05	0.00288905	frameshift-variant	CUEDC2	GRCh38.p7	10:102425128	ACCTGAGGTCGGCCT[-/C]CGGGAGGTGTGTCTG	79004
rs768014435	snp	G/T	1.67531e-05	0.00289418	missense	CUEDC2	GRCh38.p7	10:102423839	ATCCTTTTGGGGGCC[G/T]CTGAGGCGTCTGGGC	79004
rs768145119	snp	A/T			intron-variant	CUEDC2	GRCh38.p7	10:102426696	GAGTGCAGTGGTATG[A/T]TCTCGGCTCACTGCA	79004
rs768229307	snp	C/T	1.6569e-05	0.00287824	intron-variant	CUEDC2	GRCh38.p7	10:102423733	CTGTCAAAAACTGGC[C/T]GGGTGAAGCTCCTGT	79004
rs768282340	snp	A/G	1.65608e-05	0.00287752	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423600	CAGCAGTGAGTGGCA[A/G]AAGCCAGGAGCCAGT	79004
rs768512209	snp	C/T	1.66128e-05	0.00288204	missense	CUEDC2	GRCh38.p7	10:102424682	CCAGGCACATAGGCC[C/T]CCATCATCTCAGTGA	79004
rs768759478	snp	A/C	1.67697e-05	0.00289561	intron-variant	CUEDC2	GRCh38.p7	10:102424212	ACAAGAGGCAATACT[A/C]CCCCCTTTCCAGCCC	79004
rs768796511	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430246	CGATCTTGGCTCACC[A/G]CAACCTCCACCTCCT	79004
rs768963002	snp	C/G	5.10843e-05	0.00505366	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422960	GCTGCAGGATATGGC[C/G]GGCTTCGCACCTTTT	79004
rs769010008	snp	G/T	9.63159e-05	0.00693893	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422842	TGCTGCGTTCGCTGC[G/T]GGTGCGGCACTGCCA	79004
rs769014314	snp	A/G	1.6601e-05	0.00288101	synonymous-codon	CUEDC2	GRCh38.p7	10:102424509	CTCACCTTTGTTCCT[A/G]GCATCGCTCAGCTGC	79004
rs769049284	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102431820	CCCAAGGGCAGCACA[C/G]GCCTGGACCCTCCAG	79004
rs769095171	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426911	AAAGCAGTTCGCCCA[C/T]CTCAGCCTCCCAAAG	79004
rs769457340	snp	C/G	6.64022e-05	0.00576166	missense	CUEDC2	GRCh38.p7	10:102424670	ATGTGGGCGAAGCCA[C/G]GCACATAGGCCTCCA	79004
rs769481024	snp	C/T	1.66974e-05	0.00288936	missense	CUEDC2	GRCh38.p7	10:102424034	CAGGCCCCTCTTCCT[C/T]TCCCTCTACCAGCAT	79004
rs769482884	snp	C/T	4.96808e-05	0.00498377	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423565	TATCGGATCAGCTTC[C/T]TGGGGGCCTGTCAGG	79004
rs769989338	snp	A/G	1.71167e-05	0.00292542	intron-variant	CUEDC2	GRCh38.p7	10:102423905	AAGGGCACCAGCAGG[A/G]GAAACAGATGGGGAT	79004
rs770175490	snp	A/G	1.6582e-05	0.00287936	synonymous-codon	CUEDC2	GRCh38.p7	10:102424315	CCTAGTCTCTTCTTT[A/G]AGCATTTCGGGCCGC	79004
rs770194581	snp	G/T	1.94843e-05	0.00312118	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422820	ACATTGGCCGAGTAC[G/T]GCCCCGTGCTGCGTT	79004
rs770486768	snp	C/T	3.34622e-05	0.00409023	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422964	CAGGATATGGCGGGC[C/T]TCGCACCTTTTGTCA	79004
rs770543867	snp	C/T	0.000348458	0.013195	missense	CUEDC2	GRCh38.p7	10:102424526	CATCGCTCAGCTGCC[C/T]TGAGAGCTTCTGCAT	79004
rs770579158	snp	C/T			downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423239	GAAATGACCAGAATG[C/T]ACTCACACCTTCCTT	79004
rs770583891	in-del	-/T	1.67622e-05	0.00289497	intron-variant	CUEDC2	GRCh38.p7	10:102424211	AACAAGAGGCAATAC[-/T]CCCCCCTTTCCAGCC	79004
rs770717414	snp	A/G	1.65767e-05	0.00287891	intron-variant	CUEDC2	GRCh38.p7	10:102423750	GGTGAAGCTCCTGTC[A/G]CCCTGGGAAGACCCT	79004
rs770895338	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102432153	GGCACCAAGGGCATT[G/T]AGGGGAACAAGGGAT	79004
rs770956342	in-del	-/AC			intron-variant	CUEDC2	GRCh38.p7	10:102431849	AGATGCTAGATAGAG[-/AC]ACTGTGGACAAATTT	79004
rs771086543	snp	A/G	7.88239e-05	0.0062774	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422814	CTCAGGACATTGGCC[A/G]AGTACTGCCCCGTGC	79004
rs771132275	snp	C/T	3.32635e-05	0.00407807	missense	CUEDC2	GRCh38.p7	10:102425170	GGAGGGCTGCACTGA[C/T]GATCCTCTCCAGCTC	79004
rs771341685	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426905	GGGCTCAAAGCAGTT[C/T]GCCCACCTCAGCCTC	79004
rs771519542	snp	C/T	1.67649e-05	0.0028952	intron-variant	CUEDC2	GRCh38.p7	10:102424230	CCCTTTCCAGCCCCC[C/T]GGGTCCCTCATCGGT	79004
rs771696590	snp	A/C	0.000630078	0.0177381	intron-variant	CUEDC2	GRCh38.p7	10:102424425	AGAGCATCAGGTTTG[A/C]CAAGGCTCTGGGGAG	79004
rs771754097	in-del	-/CTGAGGC	1.70764e-05	0.00292197	intron-variant	CUEDC2	GRCh38.p7	10:102423959	CAAGGTGGAATGTAG[-/CTGAGGC]TACATGGTAGAGGGT	79004
rs771796975	snp	A/G	8.49899e-05	0.00651826	intron-variant	CUEDC2	GRCh38.p7	10:102425087	AGCTCCAGCACTGAC[A/G]TGAGCCTTCCGGGGG	79004
rs771991814	in-del	-/TTTT			intron-variant	CUEDC2	GRCh38.p7	10:102427947	TTGTTTGTTTGTTTG[-/TTTT]GTTTTGTTTTTGAGA	79004
rs771998414	snp	A/G			downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422833	ACTGCCCCGTGCTGC[A/G]TTCGCTGCGGGTGCG	79004
rs772046834	snp	C/G	1.65751e-05	0.00287876	intron-variant	CUEDC2	GRCh38.p7	10:102423745	GGCTGGGTGAAGCTC[C/G]TGTCACCCTGGGAAG	79004
rs772183395	in-del	-/CT			intron-variant	CUEDC2	GRCh38.p7	10:102431091	TAATCCTTACAATAA[-/CT]CTAAAATGTAGATAC	79004
rs772229582	snp	C/T	1.66225e-05	0.00288287	missense	CUEDC2	GRCh38.p7	10:102424290	TGTCTGCAGCAGCAG[C/T]AGCCGAAGACCTAGT	79004
rs772344803	in-del	-/TC			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432887	TCTCTCTTTTTCTCG[-/TC]TCTCTCTCTCTCTCT	79004
rs772500057	snp	A/G	3.31268e-05	0.00406968	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423423	CAGAGTCCGGCGAGT[A/G]CCTCAATGGAAGCGG	79004
rs772603140	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102425302	GCTATGGAACCATCT[C/G]TTGATGCTGCCCTCT	79004
rs772740342	in-del	-/C			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432728	GGCTATGGACGGGCT[-/C]CCTTGGCGGCCAGTT	79004
rs772815494	snp	A/G	1.93209e-05	0.00310806	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422844	CTGCGTTCGCTGCGG[A/G]TGCGGCACTGCCACC	79004
rs772932744	snp	A/G	4.97525e-05	0.00498736	intron-variant	CUEDC2	GRCh38.p7	10:102424430	ATCAGGTTTGCCAAG[A/G]CTCTGGGGAGCAGGC	79004
rs772959797	snp	A/G	1.6664e-05	0.00288647	synonymous-codon	CUEDC2	GRCh38.p7	10:102425135	GTCGGCCTCCGGGAG[A/G]TGTGTCTGGACAAAG	79004
rs773085004	snp	C/T			downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422923	TCGACGTGGAGCCGC[C/T]GCTGCACCAGGCCCT	79004
rs773141332	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430712	ACCCTTCCCCATCCC[C/T]GGTAGCCTTCCTAAG	79004
rs773155010	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102427598	TCCAATCAGTCGCCA[A/G]GCCCTAATCATTATC	79004
rs773283728	in-del	-/AA	1.6952e-05	0.00291131	intron-variant	CUEDC2	GRCh38.p7	10:102423987	GTAGAGGGTGCTGGG[-/AA]AAGATACCTGGTTGG	79004
rs773375208	snp	C/T	1.69922e-05	0.00291476	intron-variant	CUEDC2	GRCh38.p7	10:102425088	GCTCCAGCACTGACA[C/T]GAGCCTTCCGGGGGA	79004
rs773815230	snp	C/G/T	8.38081e-05	0.00647286	intron-variant	CUEDC2	GRCh38.p7	10:102424217	AGGCAATACTCCCCC[C/G/T]TTTCCAGCCCCCTGG	79004
rs773939359	snp	C/T	6.63119e-05	0.00575774	missense	CUEDC2	GRCh38.p7	10:102424323	CTTCTTTGAGCATTT[C/T]GGGCCGCTGCAGGGG	79004
rs774191179	snp	C/G	1.66355e-05	0.002884	missense	CUEDC2	GRCh38.p7	10:102424700	ATCATCTCAGTGAAA[C/G]CCTCCATATCGAAGT	79004
rs774252928	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428953	CATGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	79004
rs774261229	snp	A/C	3.33684e-05	0.00408449	missense	CUEDC2	GRCh38.p7	10:102424091	GAGCTTTGGCCAGCA[A/C]CCACTGGGCCTGCTC	79004
rs774440274	snp	C/G	1.65603e-05	0.00287747	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423482	ATGTGGCCTTCATCT[C/G]CTCGGCCTCAGGGTT	79004
rs774508322	in-del	-/TC			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432888	TCTCTTTTTCTCGTC[-/TC]TCTCTCTCTCTCTCT	79004
rs774680190	snp	C/G	5.2082e-05	0.00510277	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422962	TGCAGGATATGGCGG[C/G]CTTCGCACCTTTTGT	79004
rs774870538	snp	A/G	3.41507e-05	0.00413209	intron-variant	CUEDC2	GRCh38.p7	10:102423950	GCTTAACACCAAGGT[A/G]GAATGTAGCTGAGGC	79004
rs774991629	in-del	-/CAGCTC	1.7213e-05	0.00293364	intron-variant	CUEDC2	GRCh38.p7	10:102425064	CATAGTACTGCCCGG[-/CAGCTC]CAGCTCCAGCTCCAG	79004
rs775108901	snp	C/T	3.31203e-05	0.00406928	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423476	TGATGTATGTGGCCT[C/T]CATCTCCTCGGCCTC	79004
rs775298927	in-del	-/A			intron-variant	CUEDC2	GRCh38.p7	10:102429195	ACAGCCATAATTATT[-/A]TTTGGACAATGTTTA	79004
rs775516165	snp	C/T	1.66023e-05	0.00288113	synonymous-codon	CUEDC2	GRCh38.p7	10:102424672	GTGGGCGAAGCCAGG[C/T]ACATAGGCCTCCATC	79004
rs775518154	snp	A/C	1.70536e-05	0.00292002	intron-variant, utr-variant-3-prime	CUEDC2, FBXL15	GRCh38.p7	10:102422994	AACCTGCAGGTCTGA[A/C]CCGCCTGCCAATCGG	79004
rs775571142	snp	A/G	1.6585e-05	0.00287962	intron-variant	CUEDC2	GRCh38.p7	10:102424563	CCCTATTGTGCCCCT[A/G]AAAAGATGAGGGCAG	79004
rs775589050	snp	A/G	1.71158e-05	0.00292534	intron-variant	CUEDC2	GRCh38.p7	10:102423906	AGGGCACCAGCAGGG[A/G]AAACAGATGGGGATA	79004
rs775633568	snp	A/G	4.98376e-05	0.00499163	intron-variant	CUEDC2	GRCh38.p7	10:102423791	GCCCAGCCCAGCCCA[A/G]ACTCACTTCTGCAGG	79004
rs775796843	snp	A/T	1.65822e-05	0.00287938	intron-variant	CUEDC2	GRCh38.p7	10:102424416	GAGGCAAAGAGAGCA[A/T]CAGGTTTGCCAAGGC	79004
rs775859520	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428611	TTCCTTGGCTGGGCA[C/T]GGTGCCTCATGCCTG	79004
rs775904775	in-del	-/AC			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432909	CTCTCTCTCTCTCTC[-/AC]TTTTTTTTCCTTTTC	79004
rs776042261	in-del	-/CAC			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432908	TCTCTCTCTCTCTCT[-/CAC]TTTTTTTTCCTTTTC	79004
rs776083598	snp	C/T	4.96824e-05	0.00498385	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423436	GTGCCTCAATGGAAG[C/T]GGTACTTTCTGGCTG	79004
rs776120198	snp	C/T	1.92528e-05	0.00310258	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422830	AGTACTGCCCCGTGC[C/T]GCGTTCGCTGCGGGT	79004
rs776178971	snp	A/G	1.65908e-05	0.00288012	missense	CUEDC2	GRCh38.p7	10:102424543	GAGAGCTTCTGCATC[A/G]TGTCCCCTATTGTGC	79004
rs776329913	in-del	-/C	1.67657e-05	0.00289527	intron-variant	CUEDC2	GRCh38.p7	10:102424211	ACAAGAGGCAATACT[-/C]CCCCCCTTTCCAGCC	79004
rs776387931	snp	C/T	4.97789e-05	0.00498868	intron-variant	CUEDC2	GRCh38.p7	10:102424448	CTGGGGAGCAGGCAG[C/T]TGGGGGAGCGGGATT	79004
rs776390711	snp	A/G	1.70499e-05	0.0029197	intron-variant	CUEDC2	GRCh38.p7	10:102423892	CTGGTCTAGGCCCAA[A/G]GGCACCAGCAGGGGA	79004
rs776403281	snp	A/C	8.10274e-05	0.00636452	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422978	CTTCGCACCTTTTGT[A/C]AACCTGCAGGTCTGA	79004
rs776617911	snp	A/G			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433803	CCCAACAAGACTTCA[A/G]CTTCCTCTTTTTGTT	79004
rs776795755	snp	C/G	1.6577e-05	0.00287893	intron-variant	CUEDC2	GRCh38.p7	10:102423751	GTGAAGCTCCTGTCA[C/G]CCTGGGAAGACCCTC	79004
rs776855352	snp	C/T	1.66335e-05	0.00288383	missense	CUEDC2	GRCh38.p7	10:102425176	CTGCACTGACGATCC[C/T]CTCCAGCTCCATGCT	79004
rs777206591	snp	C/T	1.65855e-05	0.00287967	synonymous-codon	CUEDC2	GRCh38.p7	10:102424306	AGCCGAAGACCTAGT[C/T]TCTTCTTTGAGCATT	79004
rs777252458	snp	C/T	4.97913e-05	0.00498931	missense	CUEDC2	GRCh38.p7	10:102424514	CTTTGTTCCTGGCAT[C/T]GCTCAGCTGCCCTGA	79004
rs777700197	snp	A/G	1.69321e-05	0.0029096	intron-variant	CUEDC2	GRCh38.p7	10:102423874	CCTGCAGAGAGGGGA[A/G]GCCTGGTCTAGGCCC	79004
rs777915138	snp	A/T			intron-variant	CUEDC2	GRCh38.p7	10:102425976	GCTCCGCTCAAATGT[A/T]ACCTCCTCAGAGAGC	79004
rs777940977	snp	G/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433594	TTGGGGTGAGCTACA[G/T]GTCTGTGTCTCCGGA	79004
rs777978639	snp	C/G	1.66142e-05	0.00288216	missense	CUEDC2	GRCh38.p7	10:102424292	TCTGCAGCAGCAGCA[C/G]CCGAAGACCTAGTCT	79004
rs778098141	in-del	-/T			intron-variant	CUEDC2	GRCh38.p7	10:102425882	TGCTCCCACCCCACC[-/T]TCTGTCCCTCAGACT	79004
rs778175495	snp	C/T	1.656e-05	0.00287745	missense, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423545	TCACTACCTGGTTGT[C/T]GATGTATCGGATCAG	79004
rs778209755	snp	C/T	1.65605e-05	0.0028775	missense	CUEDC2	GRCh38.p7	10:102423698	TCTTCTGATCCTCTG[C/T]GCTATCCACCATCAT	79004
rs778210426	snp	A/G	3.3151e-05	0.00407117	missense	CUEDC2	GRCh38.p7	10:102424382	ACACCAGAGCTCTGC[A/G]GTTGCAGGTTCTCTT	79004
rs778232046	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102428066	CCTGCCTCAGCCTCC[C/T]GAGTAACTGGGATTA	79004
rs778499786	snp	A/G	1.67998e-05	0.00289821	synonymous-codon	CUEDC2	GRCh38.p7	10:102423851	GCCTCTGAGGCGTCT[A/G]GGCAGGTCCTGCAGA	79004
rs778547720	snp	C/G	1.6569e-05	0.00287824	intron-variant	CUEDC2	GRCh38.p7	10:102423734	TGTCAAAAACTGGCT[C/G]GGTGAAGCTCCTGTC	79004
rs778837600	in-del	-/A			intron-variant	CUEDC2	GRCh38.p7	10:102426896	CGAACTCCTGGGCTC[-/A]AAGCAGTTCGCCCAC	79004
rs778976097	in-del	-/GCCCA/GCCCAGCCCA	0.00026553	0.0115197	intron-variant	CUEDC2	GRCh38.p7	10:102423770	GGAAGACCCTCTAGG[-/GCCCA/GCCCAGCCCA]GCCCAGCCCAGCCCA	79004
rs779214216	snp	C/G	1.66543e-05	0.00288563	missense	CUEDC2	GRCh38.p7	10:102424278	CCTCATCTTGGGTGT[C/G]TGCAGCAGCAGCAGC	79004
rs779282075	snp	C/T			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102433279	TCCCTCCCTTCCTTC[C/T]TTCTCTTTCTTTTTC	79004
rs779314742	snp	A/G	1.65861e-05	0.00287972	intron-variant	CUEDC2	GRCh38.p7	10:102424641	TCCTGGCCCTAGCCA[A/G]AACCTACCTGGGGAT	79004
rs779335743	snp	C/T	1.656e-05	0.00287745	synonymous-codon, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423522	TTTGAATCGCTCCCC[C/T]TTGGTGCTCACTACC	79004
rs779338978	snp	A/C	8.38146e-05	0.00647304	intron-variant	CUEDC2	GRCh38.p7	10:102424215	AGAGGCAATACTCCC[A/C]CCTTTCCAGCCCCCT	79004
rs779358967	snp	A/C	0.000206996	0.0101713	missense	CUEDC2	GRCh38.p7	10:102424786	GAAGATGACCTCATC[A/C]AAGCCACTGCAGGAA	79004
rs779466393	snp	C/T	8.28246e-05	0.00643471	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423418	TCGGGCAGAGTCCGG[C/T]GAGTGCCTCAATGGA	79004
rs779646416	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102426482	GCCAAAGCTGAAACC[C/T]GGGGATTACCCTTGA	79004
rs779675669	snp	A/G	1.71926e-05	0.0029319	intron-variant	CUEDC2	GRCh38.p7	10:102424815	AAGGGAACAGGACAA[A/G]CCCTGGGTAGGACAC	79004
rs779756421	in-del	-/C			upstream-variant-2KB	CUEDC2, MIR146B	GRCh38.p7	10:102434618	TCCAGCCTGGTGATA[-/C]TAGGGTTAATGAGGG	79004
rs779781998	snp	G/T	1.65627e-05	0.00287769	missense	CUEDC2	GRCh38.p7	10:102423713	CGCTATCCACCATCA[G/T]GTACCTGTCAAAAAC	79004
rs779910614	snp	A/T	3.31219e-05	0.00406938	intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423576	CTTCTTGGGGGCCTG[A/T]CAGGCAATCAGCAGT	79004
rs779910721	snp	C/G	5.03411e-05	0.00501677	intron-variant	CUEDC2	GRCh38.p7	10:102425109	TTCCGGGGGACCCGT[C/G]TCTACCTGAGGTCGG	79004
rs780069414	in-del	-/C	1.65605e-05	0.0028775	intron-variant	CUEDC2	GRCh38.p7	10:102423641	CCGCATCCCCAGCAA[-/C]CCTTAACTCTCTCAC	79004
rs780208468	snp	C/T	1.6566e-05	0.00287797	utr-variant-3-prime, intron-variant, downstream-variant-500B	CUEDC2, FBXL15	GRCh38.p7	10:102423414	AGGCTCGGGCAGAGT[C/T]CGGCGAGTGCCTCAA	79004
rs780355378	snp	C/G	2.63779e-05	0.00363156	downstream-variant-500B, missense	CUEDC2, FBXL15	GRCh38.p7	10:102422937	CCGCTGCACCAGGCC[C/G]TGGTGCTGCTGCAGG	79004
rs780474735	snp	C/T	1.65814e-05	0.00287931	intron-variant	CUEDC2	GRCh38.p7	10:102424627	CAGCCCCTTCCTCCT[C/T]CTGGCCCTAGCCAGA	79004
rs780595242	snp	C/G	1.66034e-05	0.00288122	intron-variant	CUEDC2	GRCh38.p7	10:102424484	TCACTCAGGTGCCCA[C/G]AGCCCCAGACTCACC	79004
rs780671707	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102431493	GCACTATGAGGTTAA[A/G]TAACTTGCCCAAGGT	79004
rs780788853	snp	C/G			intron-variant	CUEDC2	GRCh38.p7	10:102426353	TCATCCCACTCAGAA[C/G]GCTCCGAGGCACCAC	79004
rs780854661	snp	A/T	1.70528e-05	0.00291995	intron-variant	CUEDC2	GRCh38.p7	10:102424800	CCAAGCCACTGCAGG[A/T]AGGGAACAGGACAAG	79004
rs781041044	snp	C/T	3.34398e-05	0.00408886	splice-acceptor-variant	CUEDC2	GRCh38.p7	10:102424180	TCAGCGCCAGTTGCC[C/T]AAGGGTACAAACGTT	79004
rs781069311	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102427453	AGTTAGCGTGTCCCA[A/C]ACTAATGTTCTCTCA	79004
rs781107687	snp	A/G	3.92241e-05	0.00442838	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422816	CAGGACATTGGCCGA[A/G]TACTGCCCCGTGCTG	79004
rs781162377	snp	A/G	1.67195e-05	0.00289127	missense	CUEDC2	GRCh38.p7	10:102424022	CCTCCCAGGCTGCAG[A/G]CCCCTCTTCCTTTCC	79004
rs781305727	snp	C/T	1.66048e-05	0.00288134	intron-variant	CUEDC2	GRCh38.p7	10:102424480	TGAATCACTCAGGTG[C/T]CCAGAGCCCCAGACT	79004
rs781511061	snp	C/G	1.65787e-05	0.00287907	missense	CUEDC2	GRCh38.p7	10:102424393	CTGCGGTTGCAGGTT[C/G]TCTTAAAGAGGCAAA	79004
rs781540798	snp	C/T	2.44981e-05	0.00349978	downstream-variant-500B, synonymous-codon	CUEDC2, FBXL15	GRCh38.p7	10:102422912	CGGCGTGGACATCGA[C/T]GTGGAGCCGCCGCTG	79004
rs781615363	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102429523	GTTGCCTGGTCCCGA[A/G]TGGTAACAGAGTTGC	79004
rs796121603	snp	A/C			intron-variant	CUEDC2	GRCh38.p7	10:102430273	TCCTGGGTTCAAGCG[A/C]TTCTCCTGCCTCAGC	79004
rs796289311	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430255	CTCACCGCAACCTCC[A/G]CCTCCTGGGTTCAAG	79004
rs796332545	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430261	GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC	79004
rs796341169	snp	G/T			intron-variant	CUEDC2	GRCh38.p7	10:102428037	ACCTCTGCCTCCTGG[G/T]TTCAAGCGATTCTCC	79004
rs796384185	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430233	GAGTGCAATGGCGCG[A/G]TCTTGGCTCACCGCA	79004
rs796468535	multinucleotide-polymorphism	CT/TG			upstream-variant-2KB	CUEDC2	GRCh38.p7	10:102432730	TATGGACGGGCTCCC[CT/TG]GGCGGCCAGTTTTGT	79004
rs796612250	snp	C/T			intron-variant	CUEDC2	GRCh38.p7	10:102430251	TTGGCTCACCGCAAC[C/T]TCCACCTCCTGGGTT	79004
rs796657109	in-del	-/T			intron-variant	CUEDC2	GRCh38.p7	10:102429836	CTTTTTTTTTTTTTT[-/T]GAGACGGAGTTTCGC	79004
rs796915379	snp	A/G			intron-variant	CUEDC2	GRCh38.p7	10:102430268	CCACCTCCTGGGTTC[A/G]AGCGATTCTCCTGCC	79004