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

EML5

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs115000783	snp	C/T	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88713929	TGCAGCCTTATCCTC[C/T]CAAGCTCAAATGACC	161436
rs115062544	snp	A/C	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88771493	CACTACTGAGTCATT[A/C]CTATTACCATTCAAA	161436
rs115066715	snp	A/G	0.02016	0.0983543	intron-variant	EML5	GRCh38.p7	14:88640613	CAAAATGTTAGAAAG[A/G]TCCCAAATTAACAAT	161436
rs115099362	snp	C/T	0.0310518	0.120672	intron-variant	EML5	GRCh38.p7	14:88639317	AAAGGCAGGAAAGTG[C/T]TGTGTATCCATATAA	161436
rs115101227	snp	A/G	0.0584853	0.160693	intron-variant	EML5	GRCh38.p7	14:88722076	GAGGTACCATCTCAC[A/G]TCAGTCAGAATGACA	161436
rs115106137	snp	C/T	0.0126979	0.078662	intron-variant	EML5	GRCh38.p7	14:88745834	AAGTCTTATACCTAA[C/T]GTAGATGATGGGTTG	161436
rs115143158	snp	C/T	0.0119091	0.0762411	upstream-variant-2KB	EML5	GRCh38.p7	14:88793823	TAAAAATGACTGGGA[C/T]ATCACCAACAGTTAC	161436
rs115197855	snp	G/T	0.0425829	0.139564	intron-variant	EML5	GRCh38.p7	14:88684225	AGCATCAAAAATAAT[G/T]GAAGTTAAAAACTCG	161436
rs115203301	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635735	GTGGTGCTATGAACT[A/G]GATGTCTGTCTTCCC	161436
rs115336472	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88678534	TAGACAAAACTGGAA[C/T]TCATGAAGGGACATA	161436
rs115388695	snp	A/G	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88643872	ACAGCAATCACCATC[A/G]CACAGCTTTACGCCT	161436
rs115392262	snp	A/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88755104	CCACCACGCCCAGCA[A/G]GTAATTTGGATTTAA	161436
rs115414047	snp	G/T	0.0185938	0.0946107	intron-variant	EML5	GRCh38.p7	14:88693819	CTCTGTTGCCCAGGC[G/T]GCAGTGCAGTGGGAG	161436
rs115422294	snp	A/G	0.0310518	0.120672	intron-variant	EML5	GRCh38.p7	14:88645666	TAGTACTGGTTAATG[A/G]CATTGCCATCAGATG	161436
rs115431878	snp	C/T	0.0456336	0.143994	intron-variant	EML5	GRCh38.p7	14:88641226	AACTATTCTAAAAAA[C/T]AGAGGAGTGGGCACT	161436
rs115449333	snp	C/T	0.0425829	0.139564	intron-variant	EML5	GRCh38.p7	14:88671582	TAAATTGGCTAAATG[C/T]CCCAAATTAAAAGAC	161436
rs115534255	snp	A/G	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88723242	ACACAGTGAGGCCCA[A/G]GCTCTACAAAAATTT	161436
rs115546251	snp	A/G	0.0498117	0.149749	intron-variant	EML5	GRCh38.p7	14:88658944	CAAAAAGTAACTATC[A/G]ATTGATTGCTTTGGT	161436
rs115548189	snp	G/T	0.0314385	0.121371	intron-variant	EML5	GRCh38.p7	14:88632287	CTGCTTAACTGTTTT[G/T]TGCTTGGACTACTAT	161436
rs115581206	snp	A/G	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88668945	AGAAGACCGAAAACG[A/G]CAAGTGAATCCTGCA	161436
rs115646431	snp	G/T	0.0391387	0.134304	intron-variant	EML5	GRCh38.p7	14:88663235	ATATAAAAACCATTT[G/T]CTGCTGCAGTCAACT	161436
rs115698350	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88726033	CTGCATAGAATTCAA[C/T]TGAATTTATCTATCT	161436
rs115753300	snp	C/T	0.0310518	0.120672	intron-variant	EML5	GRCh38.p7	14:88637883	CTGTATAATGGGTAA[C/T]GTTCCATTTACTTTT	161436
rs115760374	snp	A/G	0.021333	0.101051	intron-variant	EML5	GRCh38.p7	14:88632775	TTCTTCAGGGCGTTT[A/G]GTATTTTGGTAGTTA	161436
rs115769136	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88617091	AATTTGAAGGGTTTC[C/T]AGATTAATCTTTTTA	161436
rs115785984	snp	G/T	0.0402882	0.136092	intron-variant	EML5	GRCh38.p7	14:88763895	GATGCTTTTATAGCC[G/T]GGTTAAAGAAGTGGA	161436
rs115838979	snp	A/C	0.0205511	0.0992634	intron-variant	EML5	GRCh38.p7	14:88711090	TGAATCTCACACTTC[A/C]TAACCAGGCAAGTAT	161436
rs115897921	snp	C/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88685772	GCTTTAAATAACTTT[C/T]AGATTGCTTATATCT	161436
rs115903289	snp	A/G	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88700224	CCACTTAAGATCACA[A/G]TTACTGACAAGAGGT	161436
rs115936807	snp	A/G	0.0314385	0.121371	intron-variant	EML5	GRCh38.p7	14:88630904	ACGGAAAGTCCCTGG[A/G]TTCTGGATGACATCA	161436
rs115963898	snp	A/G	0.0240643	0.107019	intron-variant	EML5	GRCh38.p7	14:88670892	AGGATGAAAAGGAAT[A/G]AGCAAAACCTCTGAG	161436
rs115964064	snp	A/G	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88736976	ACCTTTGGGTGGGGG[A/G]TTGGGGGCAGGGGAG	161436
rs116020560	snp	C/T	0.0283406	0.115616	intron-variant	EML5	GRCh38.p7	14:88717297	AGCTTGTGACGGCCA[C/T]TGTAGTTGAATGGAC	161436
rs116022305	snp	C/T	0.0168055	0.0901129	intron-variant	EML5	GRCh38.p7	14:88663834	GCCACCATACCTGGC[C/T]AACATTTCTATATTC	161436
rs116085446	snp	G/T	0.00796007	0.0625833	intron-variant	EML5	GRCh38.p7	14:88699320	TTACAAAGAGGCAAA[G/T]AGAAAGAGATAAAAA	161436
rs116088316	snp	A/G	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88711488	GAAGTCCATGAGATC[A/G]CAGGAAAAACTACCA	161436
rs116140151	snp	A/G	0.0162398	0.0886349	intron-variant	EML5	GRCh38.p7	14:88714388	GGACTGGGAGAGGTA[A/G]AGGTTGGTGGGGGCC	161436
rs116144363	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774717	ACATTAAAATGTTGG[A/C]GTGCCACAGGAATCC	161436
rs116166158	snp	A/C	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88635022	GAAAGGAAAAAAGTT[A/C]TTTCTTTCAACTAAA	161436
rs116167396	snp	C/T	0.0948562	0.196037	intron-variant	EML5	GRCh38.p7	14:88640398	CAATACCAAGAAGAG[C/T]TCCCAAAACCACACA	161436
rs116168560	snp	A/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88689756	AAAGAGAGAGAGAGA[A/G]AGAAAGAAAAAAGAA	161436
rs116202825	snp	A/G	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88783903	TCAAGGATAGACTGT[A/G]TGTTGGGTCATAAGA	161436
rs116222903	snp	G/T	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88774216	TTGGTAGATCTGGAA[G/T]GAGCCCAGATAATTC	161436
rs116230315	snp	G/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88722565	TGGGAGCTGAACAAT[G/T]AGAACTATGGACACA	161436
rs116263204	snp	A/G	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88747420	CTGTCTCAAAAAATA[A/G]TAATAATAAGCTGAA	161436
rs116289454	snp	C/T	0.00739062	0.0603381	intron-variant	EML5	GRCh38.p7	14:88621833	GGGCATAGGGTAATA[C/T]GCATAACCATCACCT	161436
rs116323728	snp	C/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88673611	TTGCAGATGATATGA[C/T]AGTATGTCTAGAAAA	161436
rs116326080	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88658016	AAAGTCATAAATTCA[C/T]GGCAACCTGTTGTTC	161436
rs116326287	snp	A/G	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88778042	TTTTGTTTTCTCTTT[A/G]TTTATACAAACAGTG	161436
rs116357665	snp	C/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88756372	AACTGACAAAGGACA[C/T]CTACATAAACCCAAA	161436
rs116385525	snp	A/C	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88787687	TTTGATATTGCAACA[A/C]ATAAAATGAAATCTT	161436
rs116418406	snp	C/T	0.0119091	0.0762411	intron-variant	EML5	GRCh38.p7	14:88726903	CGACATCACGTCACT[C/T]TGTCACTCAGGTTGG	161436
rs116418930	snp	C/T	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88772969	TTGCTCAGAGAAGCT[C/T]TCCCTAACTACTCCT	161436
rs116478679	snp	A/G	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88741142	CACTCCAGCCTGGGC[A/G]CAGAGTGAGACTCCG	161436
rs116508824	snp	G/T	0.00795532	0.062565	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613524	ATTGTTTTTTGCTAT[G/T]TAATAGCCACTGCCC	161436
rs116510069	snp	C/G	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88683231	TAGGCCAGCTAGTTT[C/G]TCCAAGAGAACCAGT	161436
rs116513482	snp	C/T	0.0263992	0.111815	intron-variant	EML5	GRCh38.p7	14:88786848	AACCTCTTTTTCCTC[C/T]CAGTCTCAGGTATCT	161436
rs116539882	snp	C/T	0.0387552	0.1337	intron-variant	EML5	GRCh38.p7	14:88663731	TTAGGAATGGGGTCT[C/T]ACTGTGTTGCCCAGG	161436
rs116605726	snp	C/T	0.0263992	0.111815	intron-variant	EML5	GRCh38.p7	14:88740196	TACTAATTATACTAA[C/T]GTAATAAATATCAAT	161436
rs116622155	snp	C/G	0.0391387	0.134304	intron-variant	EML5	GRCh38.p7	14:88769649	TTACAAAAAATAGGT[C/G]ACACGCCAGATTGTC	161436
rs116665117	snp	A/C	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88640939	ACACCTCTAAATACA[A/C]AAACTAGAAGATCTA	161436
rs116693535	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88690940	TTGTACAATGTCCAC[C/T]AGAGCAGGTTAGCAC	161436
rs116726594	snp	C/G	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88775355	TTAGATGGCATTTCT[C/G]GACCTGCCCTGGGGC	161436
rs116757653	snp	A/G	0.0322114	0.122752	intron-variant	EML5	GRCh38.p7	14:88643884	ATCGCACAGCTTTAC[A/G]CCTTGTTTACGTTTG	161436
rs116759729	snp	C/T	0.0197687	0.0974348	intron-variant	EML5	GRCh38.p7	14:88660011	CAGATAACAGTGACT[C/T]GCGCCTGTAATCCCA	161436
rs116761706	snp	A/C	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88763628	TCCAAACAATAGAAA[A/C]AGAGGGAATTCTCCC	161436
rs116786935	snp	A/G	0.0267878	0.112589	intron-variant	EML5	GRCh38.p7	14:88687948	GGGTGGCACTTGCCT[A/G]TAGTCACAGCTACTC	161436
rs116788573	snp	C/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88695630	GGAGGGAGAATAAAA[C/G]TTTCTCAAATCCTCT	161436
rs116854750	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88780687	TTCAGGCAATTCTTG[C/T]GCCTCAGACTCCCAA	161436
rs116865094	snp	A/G	0.0119091	0.0762411	intron-variant	EML5	GRCh38.p7	14:88696565	AAACCACCTGTGGTA[A/G]CTGAGATGAATTTAG	161436
rs116977483	snp	A/G	0.0146672	0.084371	intron-variant	EML5	GRCh38.p7	14:88681669	ATTCAACAAGTTATT[A/G]GAAATTTGCTCACTT	161436
rs117011791	snp	A/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88717861	GATGGTTTCTCAGAC[A/T]TCAGAAAAAAGTGAG	161436
rs117052791	snp	A/G	0.00993419	0.0697739	intron-variant	EML5	GRCh38.p7	14:88678952	GCAGAGCTATGCTCC[A/G]TTGTGAAAGTTCTTG	161436
rs117071450	snp	C/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88626101	GGCCCAGAGCACTTC[C/T]AGCTGTATGATAAGC	161436
rs117116765	snp	C/T	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88783813	ATAGACCAAATGGAT[C/T]TAATAGATATTTGCA	161436
rs117134309	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88630505	ACTCCTTCCTAGAGC[A/G]TAAGTGATTCAGGGG	161436
rs117174690	snp	A/G	0.0178098	0.0926698	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614865	AAACAAATTTTCCCA[A/G]TAGAAAAAAGGCTAT	161436
rs117224033	snp	C/G	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88775235	CTTGAGAAAAGCGGA[C/G]TGAAAAGTAAATACT	161436
rs117301270	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707698	ACTCATCTAAAGTTA[C/T]AATTTACTGCTGCTT	161436
rs117322745	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88725931	CTGAATTGAGCAACT[A/G]AGCGAAGGATCTTAC	161436
rs117329900	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88670965	GGGTACCTGAACAGA[A/G]CAAAGTTGTAAAACG	161436
rs117347064	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88661449	TATTGAAAAACACTA[C/T]AGGATATGATATATA	161436
rs117347160	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88620984	AAGTGAAGTACTTCT[A/G]AATTATACCAGTTTC	161436
rs117395965	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88774991	GCCCTAGCTACCAGA[C/T]GACATTTTTATTCCC	161436
rs117398977	snp	C/T	0.0185781	0.0945723	intron-variant	EML5	GRCh38.p7	14:88687170	CACATTAATGAGCAA[C/T]TAATCTTTTTTTCCT	161436
rs117418816	snp	C/T	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88782099	TTCCTAGAGACTTGT[C/T]GAATGGCTTTGTCTA	161436
rs117420114	snp	A/T	0.0103295	0.0711199	intron-variant	EML5	GRCh38.p7	14:88648690	TGAAGTGGCCTCCCA[A/T]CCTCCCTTCCTCCTG	161436
rs117447998	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727558	AGGCATGCACCACCA[C/T]GCCTGTATTTTGTAT	161436
rs117454992	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88703184	ATAGTATACTACCAT[C/T]TACATAAGTATAATA	161436
rs117468336	snp	C/T	0.0494327	0.149241	intron-variant	EML5	GRCh38.p7	14:88718986	AAAATTTTAAATGAA[C/T]GTGTGATTTCTTCAG	161436
rs117523688	snp	C/T	0.0248432	0.108648	intron-variant	EML5	GRCh38.p7	14:88675178	CATAACTCCACTAGG[C/T]GGTGCCCCAGTAGGG	161436
rs117703861	snp	A/G	0.046775	0.145601	intron-variant	EML5	GRCh38.p7	14:88713326	GAACCTGGGAGGCAG[A/G]GGCTGTAGTGAGCTA	161436
rs117745497	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88708705	CTAGTGCTTGAGCAT[C/G]ATTTAATAGCACGGA	161436
rs117843005	snp	C/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88715839	GGCTAATCTTTTTGA[C/T]GTTTTTAAATAGAAC	161436
rs117869436	snp	A/G	0.0170251	0.090679	intron-variant	EML5	GRCh38.p7	14:88636370	GGAGACCTTTTAAAA[A/G]AGAAGCAAAAGGCTG	161436
rs117900105	snp	C/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88646668	AATTTTTATAAATAT[C/T]ATTTATATAAGGTAT	161436
rs117973898	snp	A/C	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88703554	CCAATTCATAAAATA[A/C]AACTGCATAGAAACT	161436
rs118043831	snp	C/T	0.00322422	0.0400215	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688310	CACTGGCCCATCATG[C/T]GCTTTCACTGTTTTT	161436
rs118071607	snp	A/C	0.0165278	0.0893908	intron-variant	EML5	GRCh38.p7	14:88637261	AAAGAATGGAGCTAC[A/C]TATATAATCTAAAAT	161436
rs118095344	snp	A/C	0.00993419	0.0697739	intron-variant	EML5	GRCh38.p7	14:88752758	ACTCTGGCCCACAAC[A/C]CCAACCCTGTACCCA	161436
rs118168277	snp	C/T	0.0248432	0.108648	intron-variant	EML5	GRCh38.p7	14:88662763	TTATCCAGTCTGGTC[C/T]TGAACTCCTGAGCAC	161436
rs118183199	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88711982	TCATTGTACAGTCTG[A/G]CTCTATGAAAGAATT	161436
rs137855583	in-del	-/A	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88748955	CAAGTGGTCTAACAT[-/A]ACAGGTAATCATGGC	161436
rs137899610	snp	C/T	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88697496	GGTTAAAGTACCAAG[C/T]ATGTCTATAGACCTG	161436
rs137907554	snp	A/C	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616313	CTCTTATTAGGAACT[A/C]TAATCTCTATGACAA	161436
rs137914608	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88700770	AGAAAGTGCCTGTAC[C/T]GGAAAGGTTAGATCG	161436
rs137918709	snp	C/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88778759	ACTCCAGCCTGGCGA[C/T]ACAGCAAGACTCCAT	161436
rs137921760	snp	A/G	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88734117	AAAAGTAAAGGAGAA[A/G]AAGATCAACAACCCT	161436
rs137927260	snp	C/T	0.021333	0.101051	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613216	GCAGCAAAGACAGAG[C/T]ACACAAGTGCATAAG	161436
rs137944834	in-del	-/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768418	TGATTGTCTTTTTTT[-/T]TTTTGAGACAGAGTT	161436
rs137996264	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88661130	GTTTTGCGCTGTCAC[C/T]CAGACTGGTGTGCAA	161436
rs138003247	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88772476	GTAAGATATACCTTC[A/G]GCCGGACGAGGTAGC	161436
rs138037382	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623524	CTCCCAGGTTCAAGC[A/G]ATTCTTCTCCTTCAG	161436
rs138038520	snp	A/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88706794	CAACCCAAGCAGCCA[A/G]AGGATCCTTTTAAGA	161436
rs138042791	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88784408	TTTAGCCACATTAAG[-/A]AAAAAAAAAACAAGA	161436
rs138045588	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783709	CAGGCCCCAATATAA[C/T]AGCTGGAGATTTCAA	161436
rs138080489	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627540	GCATAGGCCTCCACT[C/G]AATGATTGTTTCAAC	161436
rs138083393	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88780513	TTGGCTCACATGACT[A/G]TGAGGATCGACAGGT	161436
rs138084877	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752630	GCAGGGAAATACTGG[C/G]TAGAAGAAGGTGGGG	161436
rs138126512	in-del	-/GA			intron-variant	EML5	GRCh38.p7	14:88748979	TCATGGCTCTAGAAG[-/GA]GAGAAAAGACAGAGG	161436
rs138154926	snp	A/G	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88672631	TTTTTGAAAAAAATT[A/G]ATAAAATAGATCATT	161436
rs138211849	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88720717	TTGAAAACTGGCACA[A/G]GACAAGGATGTCCTC	161436
rs138221387	snp	C/T	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88720271	TAAGGAGGGACTCCT[C/T]CCTAACTCATTTTAT	161436
rs138263201	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88642527	TGCTACATTCAATCA[C/T]TATCAGAAACCACCA	161436
rs138270156	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88624058	CTTCTTAGTCAACTA[C/T]ATGTCACATTTTTTT	161436
rs138302717	snp	A/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88635623	AATGATCTGGAAGGC[A/T]GATACCAATTTAGAA	161436
rs138302767	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686908	AACAAAATATCAAAG[C/T]TGCACACAAGTTCCT	161436
rs138312227	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753302	ACAAGTCCTGCAAAG[A/G]GGTCAAGGGAACTCT	161436
rs138327051	snp	C/T	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88725502	ATATACTGTATGGCA[C/T]GGTGATACAGGAAAG	161436
rs138348046	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768437	TTTTTTTGAGACAGA[A/G]TTTCGCTCTGTCACC	161436
rs138357650	in-del	-/A	0.0205511	0.0992634	intron-variant	EML5	GRCh38.p7	14:88643377	TAGAAAATATTGGGG[-/A]AAAAAAACAATAAAA	161436
rs138364408	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612213	CCACCATGAAAACAG[C/T]ATTGGCCAAAGGTAC	161436
rs138365443	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698047	TGGCCGAGATTGATT[C/T]TATAAAAAGATATAA	161436
rs138388021	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88741497	CTTTTGTTCTATTAG[A/G]TGGAATTAGGTAAAT	161436
rs138391692	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88682820	TAATGGGGTCCTGGG[G/T]TAACCCAGGAAAAGC	161436
rs138521704	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88649830	AAATGTTTTATAGGG[-/A]AAAAAATACCTTAAA	161436
rs138530380	snp	A/G	0.0490535	0.14873	intron-variant	EML5	GRCh38.p7	14:88660700	GTGAGCCTAGATCAT[A/G]CCACTGCACTCCAGC	161436
rs138567744	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737622	AATTTTGTACCTTTT[A/G]TATCTTAGATGTGAG	161436
rs138568052	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88616962	TTCTTGGCAATTAAT[C/T]TCTAAGTACCCTATC	161436
rs138574115	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88689515	ATTACCTATTGATAT[A/C]TCTTGCCCATTTTTC	161436
rs138580894	snp	G/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88705645	TTCATTTTCAAAACA[G/T]CACTGAAAAATTAAT	161436
rs138584750	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88654538	TAATTCTGTTATTTA[C/T]CCAGTAGTAATTCAG	161436
rs138588973	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667921	CAGTGGTTCTGACCA[C/T]TCAGCTCTGGCCTGC	161436
rs138597955	snp	C/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88747057	AAGTACCGCAACTTT[C/G]ATCTATCCCTCAAAG	161436
rs138609308	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701199	GGTACTGTCTGGAGA[C/T]ATTTTAGGTTGCCAC	161436
rs138617848	snp	A/G	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88788786	ACTCTGGCTGCACAC[A/G]GTGGCTCACATCTGT	161436
rs138618539	snp	C/T	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88780030	TCTCGGCTCACTCTG[C/T]AACCTCCACCTCCCA	161436
rs138623577	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88647322	TGAGCCAAGACTGCA[A/T]GCGCCACTGCACTGC	161436
rs138645879	in-del	-/CA			intron-variant	EML5	GRCh38.p7	14:88714554	CTTAAATGTTCTCAC[-/CA]CACACACACAAAAAT	161436
rs138680117	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88771891	TCTGAATATTAAAGT[A/G]TATGAGGGCTTTGTC	161436
rs138688494	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88698717	TCAGTGGTTAAATCA[A/G]TAAATACCTCCCAAG	161436
rs138696592	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88776510	CCTTTAATAGCAGAA[C/T]TGATCAAGCAGAAGA	161436
rs138706900	in-del	-/AC	0.0501905	0.150254	intron-variant	EML5	GRCh38.p7	14:88756849	TAAATAAATGGAAAG[-/AC]ATCTCATTTCTGGGC	161436
rs138722470	snp	A/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88629366	AAAAATTAAAGGAGA[A/T]GGCAAGAAGGTGAAA	161436
rs138790766	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646006	ATTTTTATCTCAACC[A/G]TTATTCAAATACTGA	161436
rs138792440	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88677989	ACAAAGATACATGCA[C/T]ACATATGTTCACTGC	161436
rs138801717	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88760800	AAACATAGTACGCCC[A/G]CCCTCCATTTTTCAG	161436
rs138813401	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682576	TCCTCATCTGGTTGG[A/C]AACTCCGAGACTGAT	161436
rs138894313	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725059	TATTCAAATGTTATA[C/T]TCATTTTTTTAAAAT	161436
rs138914908	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88628160	TAATCTTTATACAAT[C/T]ATATGGAGAACTATA	161436
rs138920960	snp	C/T	0.0410537	0.137264	intron-variant	EML5	GRCh38.p7	14:88714096	GTCCACTGTGGCCTC[C/T]CAAAGTGCTGGGATT	161436
rs138938875	in-del	-/TT/TTTGTT/TTTGTTTGTGTGTGTGTA			intron-variant	EML5	GRCh38.p7	14:88745169	TAAATTGTGTGTTTG[-/TT/TTTGTT/TTTGTTTGTGTGTGTGTA]TGTGTGTGTGTGTGT	161436
rs138942265	snp	A/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88683438	TTTAACAGTTGGGTG[A/T]GGTCAGGGAAAGAGA	161436
rs138960773	snp	A/T	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88709024	ATTCCATTTCTTTTA[A/T]AATGTGTTTTAATGT	161436
rs138970512	snp	A/G	0.0154538	0.0865337	intron-variant	EML5	GRCh38.p7	14:88721361	ACGCTACTGAACCTC[A/G]AACTATATTACAAGG	161436
rs138989899	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88765141	AATTACCATAAATTT[A/G]GCACCTTAAAGCAAT	161436
rs139006413	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88668302	CCGGGGAGAAGCGCT[A/G]GAGCAGTCCTAAATG	161436
rs139047151	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88716062	GAAAAGGTAGGGGGA[A/G]GTAAAAATTCTTATT	161436
rs139048045	snp	A/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88632999	ATTCCACCTCATATG[A/T]CTTTTCCCTTTTCTG	161436
rs139052974	snp	C/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88717679	AAAATCACTTGAACT[C/T]GGGAGGCAGAGGTTG	161436
rs139059529	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88790882	CAGCAATTTGGGCTA[C/T]TATAATAGGTCTGTA	161436
rs139072364	snp	A/C	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88762612	ATCAATGAGACACAA[A/C]ATTAACAAGGATATT	161436
rs139088230	snp	G/T	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88648380	TTTTTTTGAGACAGG[G/T]TCTTGCTCTGTCACC	161436
rs139107578	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88694677	GTGCCATAGGGAATG[C/T]TATTTGTGGCATGAA	161436
rs139135289	in-del	-/ATTT/TTTA			intron-variant	EML5	GRCh38.p7	14:88707278	GATATATTTTATTTA[-/ATTT/TTTA]TTTATTTATTTATTT	161436
rs139181092	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766428	CTTTGGGAATGTCTG[C/T]CTTTTACAGTTGTGG	161436
rs139217531	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698817	CACCTGGAAATTATG[A/T]TGATGACTAACACTC	161436
rs139235324	in-del	-/TTA	0.0209421	0.100162	intron-variant	EML5	GRCh38.p7	14:88666627	TATGAAATGATATTT[-/TTA]TTATTAATGATAAAT	161436
rs139265755	snp	C/T	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88780678	CCTCCCAGATTCAGG[C/T]AATTCTTGTGCCTCA	161436
rs139324514	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88665143	TCACACAGAAAATTT[A/T]GTAACAGAATTGGCG	161436
rs139345134	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88733741	TACCATAAAAAACAT[C/G]AGTAATTATCTGGAA	161436
rs139362207	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88735952	AGTATTACTTATGTT[C/T]ATTTGTTATACCATG	161436
rs139369955	snp	A/C	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88710910	TAAAATTATTGTGCA[A/C]TAATATCGACTTCTC	161436
rs139384948	snp	A/G	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88774242	TCACCTGGAAAGTTA[A/G]TAAAAAATACGAATT	161436
rs139410595	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652481	CTCAAATCCCTCTGA[C/T]GAAGCTTTCCTGTAG	161436
rs139455325	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88776889	CCGTCTCAAAAATGA[A/G]AAAACAGAAACAACA	161436
rs139470180	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88675583	ATGGGAGGGGCTGCC[A/G]TGAAGACTTCTGACA	161436
rs139473497	snp	A/G	0.0170251	0.090679	intron-variant	EML5	GRCh38.p7	14:88684452	TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG	161436
rs139491475	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88722427	TACCTTGGAATACTA[C/T]GCAGCCATAAAAAGG	161436
rs139509427	snp	A/C	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88730022	AATTTTCAGTGACAC[A/C]GTTACAACTTGACAG	161436
rs139536245	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88735016	CACTGTGTGATAACA[G/T]TATTGTGGTGATGTT	161436
rs139600254	snp	C/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88726888	TTTGAATTTTTTTGG[C/T]GACATCACGTCACTC	161436
rs139626436	in-del	-/TTG	0.37971	0.233235	intron-variant	EML5	GRCh38.p7	14:88727038	CAACCTGGCTATGTT[-/TTG]TTGTTGTTGTTGTTG	161436
rs139642730	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88657647	TACAACCAGAAAAAA[C/T]GATGTAGAAGAATAT	161436
rs139652502	snp	A/G	0.0175209	0.0919426	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740517	GTCTGAAGGTCACCC[A/G]TCTTACCAAAGACAC	161436
rs139662430	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88770042	AGTCATTTAGGTTCA[C/T]TGTTCGCAACAAAGC	161436
rs139664378	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88629872	AAATCAATCCCAGTA[A/C]CTTTTCACTACCGTT	161436
rs139677260	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	ZC3H14, EML5	GRCh38.p7	14:88614050	TTCTATGTAGTTTAC[A/G]TGCTTAAGGTTACAG	161436
rs139702303	snp	C/T	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88744402	AACAGAATTAGGACA[C/T]GAAGGGAGGTGCTTG	161436
rs139702984	snp	C/T	0.0460142	0.144533	intron-variant	EML5	GRCh38.p7	14:88625480	GATCTCAGCTCACCA[C/T]AACCTCTGCTTCCCA	161436
rs139736642	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755850	AAAAATTTTTTTTAA[C/T]GAGCCAGACATAGCA	161436
rs139755648	snp	C/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88674412	CAAAGGAGAAGCAGG[C/G]ACCTTCTTCACAGGG	161436
rs139781379	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750729	AATACAGTTTGTTAT[G/T]ACTCTCCATCAAATC	161436
rs139801085	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88757197	ACTGATTTCAACAAG[G/T]GTGGTGCCAAGACAA	161436
rs139808502	snp	A/G	0.0452528	0.143452	intron-variant	EML5	GRCh38.p7	14:88619258	TAATCCCATCTACTC[A/G]GGAGGCTGAAGCAGG	161436
rs139869891	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625371	AGACAATTCTTCCCT[C/T]CCAATTCTAACATAC	161436
rs139881600	snp	C/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88652043	TGAGTATTTTACCCA[C/T]TTGTCTGACTCCAGA	161436
rs139891077	snp	C/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88702752	TCCAGTTTTACAGGA[C/T]ACTAAACAATTTTTT	161436
rs139900213	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88670082	GCACTTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	161436
rs139929360	snp	A/G	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88748406	CCTGAGGTCAGGAGG[A/G]GAGTGTCATACCTTA	161436
rs139947226	snp	A/C	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88694951	TGTAGAAAACTTAGA[A/C]AATGAAGAAAAATAT	161436
rs139948547	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	EML5	GRCh38.p7	14:88794014	GAAATCCACAATTTA[A/G]AAAGTGTTAAGTTCA	161436
rs139976090	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615112	ATGTTTTAAATGTGC[A/G]ATTACAGAGATGGCA	161436
rs139989882	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88691739	CATTTAGAGGGTTAA[A/T]CAATAGTTAGGTTAA	161436
rs140014168	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772820	TTTTTCCTTTTGTTC[A/C]CTACACTCCAGCTAC	161436
rs140020540	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88745309	CCCACCAAATACAGT[C/T]ATTGGCCATGCCTCT	161436
rs140070067	snp	A/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88746029	CTCTAACACTTTAAG[A/T]CTTTTTACATCTGTA	161436
rs140135177	snp	C/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88636914	AAACACACTGTAACA[C/G]AGAGGACAAAATGAT	161436
rs140151184	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88782794	GAATGTATGAAAATG[C/T]CTGGATCGGGCACGG	161436
rs140156516	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717529	TTTGGGAGGCTGAGG[C/T]GGGCAGATCACAAGA	161436
rs140176150	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88631496	TAAGATTGCCGGGCA[C/T]GGTGGCTCACGCCTG	161436
rs140200844	snp	C/T	0.16911	0.236552	intron-variant	EML5	GRCh38.p7	14:88762139	TGTAGGTTGCCTGTT[C/T]GCTCTGATGATAGTT	161436
rs140228839	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622500	GCAAATCCATCGTTA[C/T]GCATTATTAAGTATT	161436
rs140247575	snp	C/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88666511	GATTACAGGCATGAG[C/T]CACAGCACCTGGCCT	161436
rs140271391	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88787198	TAGGTATTATATTCT[A/G]TAAGAAACACTGTGA	161436
rs140277843	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751817	CCAGATAAAGAAGCC[A/T]CTATCCATCTTCCCA	161436
rs140290704	snp	A/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88783442	CACACTTCACCTATA[A/G]ATACACACACGGACT	161436
rs140304494	snp	C/T	0.00193048	0.0310083	intron-variant	EML5	GRCh38.p7	14:88644419	AGTAACACTGGAGAG[C/T]GAGTTTTCCTTACCT	161436
rs140309619	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88639705	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	161436
rs140312307	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88705668	AAATTAATGATTAAG[A/G]GCTATGTCAGTTGAC	161436
rs140350091	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685928	AGGATATGGAACCCA[C/T]AGATACAGAGGGCCA	161436
rs140352909	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88768987	TGTAAACCATGCATT[A/C]CCATTGGGAGCAATA	161436
rs140395726	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690643	ATAGAAGATGACAAA[C/T]TGATCAGCAACTGGA	161436
rs140398081	in-del	-/TATCT	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88726780	TAAGATAAATCTAGA[-/TATCT]TAACTATCTGTTGTG	161436
rs140400195	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88638287	TAAAAGAATACAGGT[A/G]TATTTCAAAACAGCT	161436
rs140435336	in-del	-/AAAAT	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88747710	AACTTCCAGAAACAA[-/AAAAT]AAAATAAGTTAAAAA	161436
rs140442331	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88649678	ATTTGCATTGTAGTA[A/G]TTTGTACAGTCATAT	161436
rs140474681	snp	A/G	0.0310518	0.120672	intron-variant	EML5	GRCh38.p7	14:88649978	ATATAAAAATTGATG[A/G]TGAATAGAATACAGC	161436
rs140482914	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88763894	AGATGCTTTTATAGC[C/T]GGGTTAAAGAAGTGG	161436
rs140491924	in-del	-/CACAAATTAC	0.384401	0.210799	intron-variant	EML5	GRCh38.p7	14:88765122	TTTCTATGCTGATGT[-/CACAAATTAC]CATAAATTTAGCACC	161436
rs140521211	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88697607	CAATTCTTAATTATT[C/T]CTCTAGACTCAAGTA	161436
rs140523203	snp	C/T	0.00993419	0.0697739	intron-variant	EML5	GRCh38.p7	14:88773639	GAAACAAACAACAAA[C/T]GATACCTGGACCCCA	161436
rs140532812	snp	C/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88686683	GAGTATGGTGGCAGG[C/T]GCCTTTAGTCCCAAC	161436
rs140571124	snp	A/G/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88682583	CTGGTTGGAAACTCC[A/G/T]AGACTGATGCAACCA	161436
rs140637397	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88728237	CCTAAACAATATAGT[A/G]TAACAACTATTTACA	161436
rs140639130	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615946	TGCTTTCAGGTTACA[C/T]GTGTAATATTTTTCC	161436
rs140645123	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88700526	ATCAAGGAATTCTTC[C/T]AACGACTTAACTTTA	161436
rs140688839	in-del	-/AT/TA			intron-variant	EML5	GRCh38.p7	14:88729089	TCATATATATATATA[-/AT/TA]ACCAACTGAGAATGG	161436
rs140713943	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88620479	GGGAGATACCTCTTG[A/G]TGGGATGAACTTAAT	161436
rs140722879	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662926	CCAATATTTTAATAA[C/T]TTGAGAACAGACTTC	161436
rs140773218	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88785316	TTAATTGTACATTTT[A/G]GAATAACTAAAAGGT	161436
rs140776166	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88705251	AATGTGAGTATACTA[C/T]GACAAAATCCTATAG	161436
rs140797206	snp	C/G	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88667597	CTCAGTTCCAAATCT[C/G]CCACTTTGGGCCTCA	161436
rs140811825	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88658943	ACAAAAAGTAACTAT[C/T]GATTGATTGCTTTGG	161436
rs140813921	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88709843	AGCAGTGAAAAAAAG[A/G]CATTAAAGCTACACG	161436
rs140816482	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622256	TGTTTGTTTACTGCA[C/T]GTTTTATCTAGGGAA	161436
rs140853433	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703053	TGCCCAGCCTGAACA[A/G]TTAAAAAAATACCAC	161436
rs140860806	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88727201	AATTTTATCTTTTTC[C/T]TCTTATGTCAACATG	161436
rs140865423	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88781612	TAATCCCCAGACATG[A/G]GAGGGACCTGGACAA	161436
rs140868386	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88700848	ATATAGGATAACCAG[C/G]TAGTTTTAACCTCTA	161436
rs140868490	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750972	GTCTCCTCTGTCTGG[C/T]ATAGCTCATCAAATA	161436
rs140906242	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746655	ACCTGGAGGATGAGA[A/G]AACACCTACACCTAC	161436
rs140928511	in-del	-/TTTG			intron-variant	EML5	GRCh38.p7	14:88760351	GTTATAGTTGTTTGT[-/TTTG]TTGTTTGTTTTTTGC	161436
rs141073246	snp	G/T	0.0107246	0.0724382	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612021	TATTTGGGGCATGTT[G/T]GTGCACTGCTGTTGT	161436
rs141114035	snp	A/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88774807	TTAAATACTGTCTAT[A/G]TGCTGATAACATTCA	161436
rs141120425	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660327	TGTATCTGGACTTGA[C/T]ATATAAATTTTATTT	161436
rs141146259	in-del	-/CTCGGC			intron-variant	EML5	GRCh38.p7	14:88684237	AATGGAAGTTAAAAA[-/CTCGGC]TCACTGCAAGCTCCG	161436
rs141184293	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694233	TCTAGGGTACACACT[C/G]CACTTAGCTAAATTA	161436
rs141206437	snp	A/G	0.040671	0.13668	intron-variant	EML5	GRCh38.p7	14:88739942	TTACTTTGTAAGGGG[A/G]ACCCAAACTGCTAAA	161436
rs141242474	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88645539	TGAAAGTGAATTTTC[A/G]TAATATTTCTATGAA	161436
rs141271412	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88676435	TTAGACTCACTATCA[C/T]GAGAACAGCACGGGA	161436
rs141278731	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88724207	TTGAACCTGGGAGGC[A/G]GAGGCTGCAGTGAGC	161436
rs141281002	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88770142	CTTACAGTCATTTTG[C/G]AGTTTTGGTATTCTC	161436
rs141298532	snp	A/C	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766938	TAGCACACAGTTATA[A/C]CAAATGTTTTACATT	161436
rs141304942	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613843	TTAAAAAAGTAAACA[C/T]AGGGCAGATTCTATA	161436
rs141310269	snp	A/G	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88722825	AGGTGATGGGTTGAT[A/G]GGTGCAGCAAACCAC	161436
rs141355887	snp	A/G	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88672038	CTTGAACTCAGCTCC[A/G]GATCAAGCGGACCTG	161436
rs141357275	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743659	AGGTCTACTCATGTT[C/G]CTTCTCCCACACCAT	161436
rs141385856	snp	C/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88662269	TTAAGCCTCTCTTCC[C/T]AGGCCAAGATAAAAA	161436
rs141397264	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88720166	CTACCAACCAAAAAA[G/T]GCTCATGACCAGATG	161436
rs141425336	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634982	AGCTGAGAGACATGA[C/T]GGCAAAGCTTACTGT	161436
rs141455356	snp	A/G	0.0256215	0.110247	intron-variant	EML5	GRCh38.p7	14:88625698	TGAGCCACTGTGCCC[A/G]GCCTGAGCCACGGTG	161436
rs141457734	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88684529	ATGAAATTTTAGCAT[A/T]CATTTTTATTTTTTC	161436
rs141470181	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710011	ACAGAGGGGGTCTTG[A/G]CCATTATTAACAGTG	161436
rs141510097	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88643883	CATCGCACAGCTTTA[C/T]GCCTTGTTTACGTTT	161436
rs141517217	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755644	GATGAACAAGAAAAT[C/T]ACACCTGGCATCACG	161436
rs141558273	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689049	TGTTATAGAGTTTTT[C/T]ACATGTTAGAAAACT	161436
rs141561694	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767404	CCCCTACAATTTTCC[C/T]CATAATTTCCAGCTC	161436
rs141645795	snp	A/G	0.0879971	0.190408	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766185	CTGCACAAATTGTTT[A/G]AACAATATGAAATCT	161436
rs141660327	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651697	CTTCAAATATTCTAA[C/T]TAGAATATTTAAATA	161436
rs141666149	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88734330	ATAATGAGTGGTAAA[C/T]GTAAGTATTAGAATG	161436
rs141686401	snp	A/C	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88775846	CTGACCCAGCACCAT[A/C]ATAGTGGTGGTGGCC	161436
rs141691286	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88655425	AACTAGCTACCCGTA[C/T]GTAGAAAACTGAAAC	161436
rs141724580	snp	A/C	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88740899	CAGGCACAGTGGCTC[A/C]TGCCTGTAATCCCAG	161436
rs141725629	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88701492	GTACATAGAATGTGC[C/T]TGATGAATGTTTTTG	161436
rs141729197	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88652356	GACTTCCCTGGCAAC[A/G]CGGGGGTCAGTCAAT	161436
rs141766478	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88659679	CTACACCATCTGGAA[C/T]GCTGGAAGTGAAGTT	161436
rs141770148	snp	G/T	0.000111607	0.00746934	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657393	TTCATCAATTGAGGG[G/T]TCTTTTTGTTGTAAA	161436
rs141779440	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88776647	GCACTTTGGGAGGTC[A/G]AAGCAGGTGAACTGC	161436
rs141787235	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88702431	TCTGGCTTATTGTCA[C/G]TCTTTCAAACCTACC	161436
rs141822903	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698753	CTCTCGAGCAGTTAC[C/T]TTTCCTCTGAATCCA	161436
rs141829923	snp	A/G	0.0263992	0.111815	intron-variant	EML5	GRCh38.p7	14:88677268	CAGAAAATTGAAGCT[A/G]GACCCCTTCCTTACA	161436
rs141837691	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784424	AAAAAAAAAACAAGA[C/T]ACAAATAAAATTGGA	161436
rs141857574	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88778247	GACAATGAAACAACA[A/G]GAAAACAAATAACAA	161436
rs141933640	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683162	TTGTAAAAAATCTAA[G/T]AAAAAGTAATTGGGA	161436
rs141944032	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791927	TAAAGGGTTTCCCCC[A/C]ACCCCGGGTGCTTTA	161436
rs142036563	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786321	ATTTACACACATATA[C/T]AAAATTTACCTTCTT	161436
rs142055835	in-del	-/ACAC			intron-variant	EML5	GRCh38.p7	14:88716733	GTCCACTGCTCACCA[-/ACAC]ACACACACACACACA	161436
rs142056228	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88679202	ATTATATCTGCTAAT[A/G]CTCTATTTCTAAATG	161436
rs142058929	snp	C/T	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88762171	ATAAATGTATATGCA[C/T]CCAATACAGGAGCAC	161436
rs142104557	snp	A/C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88633990	TCATTAAAAAAAATC[A/C/T]GCAAGTTTTTTATAG	161436
rs142124300	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672888	TCTGAAATTTAGGCA[A/G]TAATAAATAGTCTAC	161436
rs142130316	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88725206	TTCCATTTGGGAAGA[C/T]GAAAAAGTTCTGAAG	161436
rs142149691	snp	C/T	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88763247	AGATAACAAAATAGA[C/T]AGACAGCTAGCAAGA	161436
rs142151065	in-del	-/TATGAT	0.378372	0.214524	intron-variant	EML5	GRCh38.p7	14:88695210	TCTGAAATCATTTAC[-/TATGAT]TATATTATTTATTCA	161436
rs142163176	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88685606	CATATAACCCACATA[C/T]ATCATTCCATATATT	161436
rs142192304	snp	C/G	0.00125252	0.0249938	intron-variant	EML5	GRCh38.p7	14:88627994	GGAAAAGGAGTTTTG[C/G]GGGTGGGGAGGAAAG	161436
rs142192772	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88680981	ACACAGCAAAATGAG[A/G]TCCTTGGAGACAATT	161436
rs142220225	snp	C/T	0.190519	0.242821	intron-variant	EML5	GRCh38.p7	14:88721538	CTCCTATTCAATAAA[C/T]GGTGCTGGGAAAACT	161436
rs142228970	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88775905	TTTAGGTGGCTCAGA[-/AG]AGAGAGAGAGAGAGA	161436
rs142239775	snp	A/G	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88759026	ATAAGGACTGCTAAT[A/G]AGCTTGGGAATTTTT	161436
rs142288977	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697248	ATCTATTGTTTGTAT[A/G]CTAGATACAACGAGC	161436
rs142334130	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760609	CTGTGAGTCCTCTAC[A/C]TTTGTTCTTTTTCCA	161436
rs142357693	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88740829	ATTATTTTTAAAATA[C/T]GCTATGCTTTCCTTA	161436
rs142374840	snp	A/G	0.000248783	0.0111503	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625056	GTGAGCTCTCGCCAC[A/G]ATTCTACACAATATG	161436
rs142406159	snp	A/G	0.000798403	0.0199641	intron-variant, missense	EML5	GRCh38.p7	14:88616553	AAGATGGTATTACTC[A/G]AGGGAGAGGATTTGT	161436
rs142459678	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88631811	AAACCCAAAGTGCTA[C/T]GATTACAGGTGTGAG	161436
rs142467019	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88745601	ACCATAATACATATG[C/T]AACAAATTAGTGGTA	161436
rs142468473	snp	C/T	0.0197687	0.0974348	intron-variant	EML5	GRCh38.p7	14:88653121	TGGTGTAGAGGAATG[C/T]TTGTGATTTTTGCAC	161436
rs142496269	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613680	GGAAGGAAATGAGCA[C/T]GGTTGGCGATTGGAA	161436
rs142504044	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637724	GAGGCATTGAGCTAG[A/G]TACTTAGGTAACATA	161436
rs142505551	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698557	GGCATGAGCCACGGC[A/G]CCCAGCTTCCTTGAC	161436
rs142506544	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88722206	TGGAAGATGGTGTGG[C/T]GATTCCTCAAAGATC	161436
rs142521040	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88777646	ACTTTTTAAGACATA[C/T]GCAGTACAATAAGAT	161436
rs142524571	in-del	-/A	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88635883	TAATCTTTTTTCACC[-/A]TGTGAGGATATAATG	161436
rs142543867	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88694772	ATTCCTCTTAAACTA[C/T]TGTTAATTTGAGCAT	161436
rs142557780	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88650459	ACTCTGTCTCAAAAG[A/T]ACAAAACAAAACAAA	161436
rs142561791	snp	C/T	0.0322114	0.122752	intron-variant	EML5	GRCh38.p7	14:88699839	GAAGGAAACACGAAA[C/T]GATGAACAGGTTTGG	161436
rs142592663	snp	A/G	0.0170251	0.090679	intron-variant	EML5	GRCh38.p7	14:88758487	GGCATGAGCCACCGC[A/G]CCTGGCCCACTTCTA	161436
rs142605746	snp	A/G	0.0107246	0.0724382	intron-variant	EML5	GRCh38.p7	14:88774135	AAAAAGCAAAAAACA[A/G]AAAACAAAAAACAAA	161436
rs142634209	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88769913	AAAGACAGTTCAGAA[C/T]TGGTAGCCCTGTGGA	161436
rs142639538	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88740122	ATTGAAGTCAACAAG[C/T]TTTTTTTCAACACTA	161436
rs142660720	snp	C/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88691632	TCATAACTTGAAATT[C/T]TCAAAGCCTAGATCT	161436
rs142684354	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88647557	CAACAATTAGCCAGG[C/T]CTGTGGCACCTATAG	161436
rs142692427	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729778	GTTGGCCAGGCTGGT[A/C]TTGAACTCTTGGCCT	161436
rs142712974	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771953	TTCATCCAATCCCAC[A/C]GCTTTAAATGCATAT	161436
rs142757371	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88769290	TTCTCATGATAGTGA[A/G]TTCTCATGAGATCTC	161436
rs142791096	in-del	-/TACTC	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88726103	TTAAATTTTTCTAAT[-/TACTC]AAACAAAAGAAGAGA	161436
rs142822796	snp	C/T	0.0221141	0.102801	intron-variant	EML5	GRCh38.p7	14:88736086	GCGCACTGCAACCTT[C/T]GCCTCCTGGGTTCAA	161436
rs142825923	snp	A/C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88642832	AAAGATTTTAAGCTG[A/C/T]TAGATCAAAATTTCT	161436
rs142854919	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652898	TTGGGCAGTATGGCC[A/G]TTTTCACGATATTGA	161436
rs142873203	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88669056	GGTGGAGTGACAGCC[C/T]ACCTGGGAGCTGCAC	161436
rs142875080	in-del	-/TT	0.16911	0.236552	intron-variant	EML5	GRCh38.p7	14:88791087	AATCTCAATTTTGTC[-/TT]TTCTTATCTTTACTC	161436
rs142880145	snp	A/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88777468	AAAAGGACATTAATG[A/T]GCAATAAGTAATCCC	161436
rs142893944	snp	A/C	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88636044	TGGTATCTGTCATGG[A/C]AGCTCAAATTTCTTA	161436
rs142943829	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88764522	CTAGCTAGAAGTTTA[C/T]CAATCTGATCCTTTT	161436
rs142944625	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88714318	ATCTGTTTTAGATCC[C/T]CCAGCCAAAGCAGTT	161436
rs142984476	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88668316	TGGAGCAGTCCTAAA[C/T]GCAGAGTGCAGGAAG	161436
rs142985282	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782994	TGAAACAGAAGAATC[A/G]CTTGAACCCAAGAGC	161436
rs142985488	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88761531	AGGACATGAACTCAT[C/T]CTTTTTATGGCTGCA	161436
rs142988479	snp	A/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88747661	GAATACGAGACTATA[A/T]AAAGTATCCAAGGAG	161436
rs143028608	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88790928	ATACAGAGTCCCAGC[C/T]TGAGAAAAATGAAAT	161436
rs143050513	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88739135	ATAAGAATAAACAAA[C/T]ACATCAGAAAACACA	161436
rs143063905	snp	C/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622379	AGATTCTAGAAAATA[C/T]TGGAGGTTTACATAC	161436
rs143125706	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88785702	TCTTCAAAATACATA[A/G]AAATTTGCTCTTTTG	161436
rs143159012	snp	A/G	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88711857	AGCTGAGGCAGGAGG[A/G]TTGATGGAACCCAAG	161436
rs143194672	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676882	AAAAACAAGCAATGG[A/G]GAGAGGATTTCCTAT	161436
rs143197885	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88707549	TGATATTGTTTTAAA[C/T]ACTTTATATTAAGTT	161436
rs143234705	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88682301	TGGAGAGAATAGGAA[C/T]TGGCTGCTCTGCAAT	161436
rs143317471	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88688812	AATGCCTATATATCC[A/G]CTGACCTACAAAAAG	161436
rs143318844	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88733766	CTGGAAACAATTAGG[C/T]TGAGTCCCCATCTTA	161436
rs143356289	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651033	CCATGAACCATATTA[C/T]CTCCTCACAAATATT	161436
rs143362858	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733589	ACAATGAAAGGATTA[C/T]GAATAGCTCCTAGCA	161436
rs143405920	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88689908	TACTGTGCTAGATGA[C/T]GATGGGTGCTTTGGA	161436
rs143463347	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698323	CCTGCTGAAGTGAAA[C/T]GGCATGATGTTGGCT	161436
rs143470518	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775297	TAGGGGTGGGTAGAT[C/G]ACCAAGTGGGATCTT	161436
rs143495870	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695171	TTAAAAGTGGGTTCA[C/T]AAGGGATAAATCTAC	161436
rs143498940	snp	C/G/T	0.0879971	0.190408	intron-variant	EML5	GRCh38.p7	14:88772614	AAAAATTAGCAAGGC[C/G/T]TGGTGGTGCGTGCCT	161436
rs143503644	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627483	GTTCCACTGGGCTTT[C/T]AAAGTGAAATATACC	161436
rs143507757	snp	A/C	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88713215	TGGCCAATATGGTAA[A/C]ACTCCATCTCTACTA	161436
rs143531992	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730635	TTAACAGATGTTACA[C/G]ATACTACTCAATTGT	161436
rs143579075	snp	A/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88649697	GTACAGTCATATGTA[A/T]AACAATTTATCATAA	161436
rs143585249	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777014	GACAGGAGTAGAAAG[C/G]TTATTCAAAGTGATA	161436
rs143606729	snp	C/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88634601	AAATTGGTTTTATTA[C/T]ATTTGATTGAGTAAA	161436
rs143629351	snp	C/T	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88773464	CACATTGTCATATAA[C/T]GCATAATAGTAAATG	161436
rs143629819	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88723533	AAGATATACTGTATG[A/G]CACAGTGATTAGAGT	161436
rs143641960	in-del	-/ATTTT	0.0174175	0.0916809	intron-variant	EML5	GRCh38.p7	14:88663263	ACTTATAGTAAGAAC[-/ATTTT]ATTTTTATAATTCCA	161436
rs143690348	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88623648	CAAACTCCTGACCTC[A/G]TGATCCGCCCACCTC	161436
rs143735547	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752947	CACTTCCATTGCTCA[A/G]TAAAATCCTCCATAT	161436
rs143739323	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88728289	TATTATAAGTAATCT[A/G]GAGATTTAAAGTACA	161436
rs143763740	snp	C/G	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88646159	TCCAACATTTATGAA[C/G]AAGTCTCATAAAATT	161436
rs143779575	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660041	ACCACTTTAGGATGC[C/T]GAGGCAGGAGGATCA	161436
rs143781118	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88672354	TTGAAACCAATAAGA[A/G]CATGGAGACAAGATA	161436
rs143781123	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617684	TTGCCCAGGCTGGTA[C/T]CAAAACTTCTAGGCT	161436
rs143815817	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624163	TCACTAAAGCCTTGA[C/T]CTCCCCAGGCTCAAG	161436
rs143821884	snp	A/C	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88709479	AGAAAACACAGAAGA[A/C]CAAAACATATTTTAA	161436
rs143851674	snp	A/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88725797	AAGCCTACACAAGAG[A/T]ACAATGGTGAGAATA	161436
rs143859106	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88684534	ATTTTAGCATACATT[C/T]TTATTTTTTCTTAGA	161436
rs143875494	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88670083	CACTTTTGGGAGGCC[A/G]AGGCAGGTGGATCAT	161436
rs143908352	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88717543	GCGGGCAGATCACAA[A/G]ATCAGAGAGAGACCA	161436
rs143912528	snp	C/T	0.021333	0.101051	intron-variant	EML5	GRCh38.p7	14:88666378	ATTACAGGCATGTGC[C/T]ACCAGGCCTGGCTAC	161436
rs143920352	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749075	CCACAAATTTAAGAC[A/G]TTCAACAAATCCCAA	161436
rs143920501	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794389	GTCATGAAAAGTAAA[C/T]TCTGAAAGAGTTTCC	161436
rs143987956	snp	A/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88648770	GAGATCAGTACTGAG[A/T]AAGCTATTCTAGATG	161436
rs144001230	snp	A/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88731077	TAATGTCTTTTTATA[A/T]TATTATTATGCTTTG	161436
rs144040142	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88772484	TACCTTCGGCCGGAC[A/G]AGGTAGCTCATGCCT	161436
rs144053594	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647071	ATGCAGACAGCTATA[C/T]TGCATAATATTAAAG	161436
rs144057069	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88787502	TTATAAAATAATAAA[A/G]GAAAATAATTAAATG	161436
rs144072919	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88661911	TAAACATTTTTCTTT[A/G]TAGTTATGTGTGTCA	161436
rs144100442	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88771777	TAACTGACCACCCAC[A/G]TTTTTGAAAGACTTT	161436
rs144149592	snp	A/C	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88693614	TAAATGGCAATAAAT[A/C]TTGTATTTGTTTAAA	161436
rs144155688	snp	A/G	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88735987	AATAAAGTTTTAATC[A/G]GAGTATTTTTTCTTT	161436
rs144175961	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88770083	AGGAGAGGAAAGAGC[A/G]CTTGTGAAACGGCCG	161436
rs144197391	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88692015	AATACTGAGTAAAAT[C/T]GGCCTTCCATGTTCT	161436
rs144275001	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88755147	CTATAAAAATCCATG[C/T]TAACAGTTACTACTT	161436
rs144277481	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726709	TAAAAAATAAAAAAG[A/G]TTAGCTAATGCATAC	161436
rs144298845	snp	A/G	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88672778	TATGCAAATAAAATA[A/G]AAAATCTGGAAGAAA	161436
rs144307509	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88638420	CCCCCACGGAAGCAG[A/G]GTTCTACCCCGCCCA	161436
rs144315929	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88722699	AGTGCTCCATTACTG[A/G]AACGCTAAGCTTGTG	161436
rs144402537	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678818	TTGAACACTGGAATA[C/T]GAACACAGTATTGGT	161436
rs144425114	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765997	TAATTTCTTATGCCT[A/G]TCTTTACTGCAATCT	161436
rs144467179	snp	A/G	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88625559	AGCGCCAGCCACCAC[A/G]CCCGGCTAATTTTTG	161436
rs144507384	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88621710	GAAGATAATATCCGT[A/T]TGATTTATAAATACA	161436
rs144507515	snp	A/G	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88674497	GATGTCGTGAGACTC[A/G]CTATCACGAGAACAG	161436
rs144522333	snp	A/C	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88756357	AAGGAAACTTCCTCA[A/C]ACTGACAAAGGACAT	161436
rs144524844	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88691351	TTGTTCTATAATTAC[C/T]TACATAATACCCTTG	161436
rs144556816	in-del	-/A	0.476314	0.106217	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626617	GTGAGATACTGTGTC[-/A]AAAAAAAAAAAAAAT	161436
rs144568994	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702063	GTAAAATAAAGAGAC[A/G]TAGTCCTTTGGTTTG	161436
rs144574146	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88735543	ATTATAATTAGTTCT[C/G]TTAAGGGTGTGAGAA	161436
rs144582945	in-del	-/A	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88652457	GAATATAAAATCCAT[-/A]GGTGCAAACTCAAAT	161436
rs144622692	snp	C/T	0.00510865	0.0502815	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705517	GTGTCTCTTGTTCAA[C/T]TTCAGAATCCAGTTC	161436
rs144680502	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88616930	AAGTGCGGGCAGGTT[C/G]ACTATATTCAAAAAG	161436
rs144680945	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777027	AGGTTATTCAAAGTG[A/T]TAACAACAGAAAAAG	161436
rs144685681	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663697	ATTTCTTTTTAAAAA[A/T]GTATTTCATTTTTTT	161436
rs144695064	snp	A/C	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88701134	TACCAGGCTTTGTAC[A/C]TATTTCTACATTTAA	161436
rs144695156	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88751161	CTATGCATAGATTAC[A/G]CAACAACAGACAGGA	161436
rs144702969	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699243	GGAACTAAGTAAAAG[A/G]TGTGAAATAGCATTA	161436
rs144723278	snp	A/C	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88659192	AGAGATGTCTTATAC[A/C]AAACACAGTGATAGC	161436
rs144732765	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88746930	GCTGGCCTAAATTCT[C/G]ATTAAACATGAATCC	161436
rs144776535	snp	C/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88782302	GGGTATCTGGTGGAA[C/G]AAATTTCTAAGCGAC	161436
rs144847302	in-del	-/AAGTA	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88756432	GAAAGCAATCCCACT[-/AAGTA]AAGGGAAAAAACAAG	161436
rs144851723	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88637162	AATAAAATCCTTTCT[C/T]ATTCTTTAGTCTTCC	161436
rs144854123	snp	C/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88700459	CAAACCAGGAGCATC[C/G]CTGAGTTATTTTCAG	161436
rs144865401	snp	C/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88777897	GGAGGGTCACCTGAG[C/G]CTGGGAAGTCAAGGC	161436
rs144916354	snp	A/G	0.0402882	0.136092	intron-variant	EML5	GRCh38.p7	14:88671397	CTTGCAAGAGCTCCC[A/G]AAGGAAGCACTAAAT	161436
rs144940144	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718656	AGCAGAAGGCATATA[A/G]GAATGAGGATAGAGG	161436
rs144944647	in-del	-/AGAG	0.0912693	0.193144	intron-variant	EML5	GRCh38.p7	14:88775906	TTTAGGTGGCTCAGA[-/AGAG]AGAGAGAGAGAGAGA	161436
rs145021042	snp	C/T	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88728032	GCTTAAAATCAAAAC[C/T]TGTGAAATATAGCTG	161436
rs145063828	snp	C/T	0.00180495	0.0299869	intron-variant	EML5	GRCh38.p7	14:88643051	AATAAAACCATTATA[C/T]TCTTCCTCATGTATA	161436
rs145067717	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770392	TTAAATTTTATATAT[A/G]GTGAGGTATATGCTG	161436
rs145081544	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723261	CTACAAAAATTTTAA[A/G]AAATAATTTTAGAAA	161436
rs145086270	snp	A/C/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767149	ATTTATTTCAGCAGA[A/C/G]AAGCAATCCAATTAG	161436
rs145103378	snp	C/T	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88684459	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTGTTT	161436
rs145165433	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88727447	GTTCCTGTTGTCCAG[A/G]CCGGAGTGCAATGGT	161436
rs145229922	snp	C/G/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615997	GTATTTGCATAAATA[C/G/T]GAGATTCTGAAGAGC	161436
rs145263179	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88723160	GCTCATGCCTGTAAT[C/G]CCAGCACTTTCAGCA	161436
rs145272291	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88666549	TAAAATATTTTTAAA[A/T]ATCTAATAGGCCATT	161436
rs145276541	snp	G/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612752	CTGCAAGATAGATAG[G/T]ATGAAACTTTTGGCC	161436
rs145282623	snp	C/T	0.00381121	0.0434866	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746208	TATGACCAGGAGCCA[C/T]AGACAACATTTTTCC	161436
rs145319628	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88732544	GGATTGTCTTGGCAA[C/T]GTGGGCCCTTTTTTG	161436
rs145355460	snp	A/G	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88745501	ATATTCTAACAAGTC[A/G]TCAGTTAAAAATGTT	161436
rs145358472	snp	A/G	0.0107246	0.0724382	intron-variant	EML5	GRCh38.p7	14:88774128	TGTCTCAAAAAAGCA[A/G]AAAACAGAAAACAAA	161436
rs145367266	snp	C/G	0.0127156	0.0787153	intron-variant	EML5	GRCh38.p7	14:88661095	GGATAAAAGGAATGT[C/G]TCTCTCTCTCTGACA	161436
rs145371600	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88742229	CAATATTGACCAATA[A/G]AAATTTCAGTGATGA	161436
rs145378769	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666154	ATGATATATGTGGAA[A/G]TTTTGCAGAGTAGGT	161436
rs145402819	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88786275	TTCCTTAGCTCTTAC[A/G]AACTATACATATATA	161436
rs145409322	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783482	AGGATGGAAAAAGAT[A/G]TTCCATGCCAATAGA	161436
rs145416512	snp	C/T	6.33513e-05	0.00562776	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618771	AAATCCACTGAGTTC[C/T]CACTAGAACCTACTG	161436
rs145422633	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88702958	TGGGGTTTTGCCATG[C/T]TGCCCAGGCTGGTCT	161436
rs145454031	snp	C/T	0.0154538	0.0865337	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615254	TAAAAAAGGACCTTA[C/T]TAATGCCTAAAAAAC	161436
rs145460883	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88699451	GTCTGACTCTCCAAC[C/T]TCCCCTTTTTATCTC	161436
rs145501068	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88676366	TCACAGGGTGGCAGG[A/G]TAGAGTGAGTGGAAG	161436
rs145502261	in-del	-/T	0.0501905	0.150254	intron-variant	EML5	GRCh38.p7	14:88738397	GTTTTATTACATCAA[-/T]TTTTTTTTAATCCCC	161436
rs145506547	snp	A/G	0.0399052	0.1355	intron-variant	EML5	GRCh38.p7	14:88758057	AGATGGGGTCTCCCT[A/G]TGTTGCCCAGACTGG	161436
rs145553065	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745350	AGGTTAGGATTTTAC[G/T]ACATATACATACACA	161436
rs145589932	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88741031	AGCCAGGTATGGTGG[C/T]GCATGCCTGTAATCC	161436
rs145611523	snp	C/T	0.0119091	0.0762411	intron-variant	EML5	GRCh38.p7	14:88681122	AACAAATAGAAGTTA[C/T]AAAAATGACAATTAT	161436
rs145632714	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641761	CCAAATATAATAAAA[A/G]CTAAAGCAGGTGGCC	161436
rs145653462	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88635522	CTTGAATGTCATCGG[C/T]CTAAATATTTTAAAG	161436
rs145653472	snp	A/G	0.0115144	0.0749975	intron-variant	EML5	GRCh38.p7	14:88686706	GTCCCAACTACTCAG[A/G]AGGCTGAGGCAGGAG	161436
rs145658728	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766537	TTGGTCAGACCGGTC[A/G]TCTGCTCTCAAACCC	161436
rs145688756	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88652791	CTTTTTATTGTTTAC[C/T]ACCTTTGATTTTGAA	161436
rs145707113	snp	A/C/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88682622	AGGCTCTCTCTCCCC[A/C/G]CAGCTCGCGGTCAGA	161436
rs145716182	snp	C/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88694015	TAGGCTCAAGTGATC[C/G]TCCCACCTTGGCCTC	161436
rs145726540	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771869	GCACTATCTCCTGCA[C/T]CCCACCTCTGAATAT	161436
rs145777298	snp	A/C	0.00517822	0.0506191			GRCh38.p7	14:88770745	CTAGTATATTGCTGA[A/C]CATATAGTAAAAACT	161436
rs145779956	in-del	-/T	0.02016	0.0983543			GRCh38.p7	14:88638392	TTGGGTCCTCTCTTC[-/T]TTCCAGCCTGAACCC	161436
rs145799607	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88692501	ATATTAGGTATTATC[A/G]GTAGTCTAGAAATGA	161436
rs145834067	snp	A/C	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88620193	CAAGCTTTTGACAGA[A/C]CTAGATTCAATAATC	161436
rs145838793	snp	C/T	0.0146672	0.084371	intron-variant	EML5	GRCh38.p7	14:88703419	ATACAACGTATATTC[C/T]AAAAATAAGTTTAAA	161436
rs145858557	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88750323	AGAATCAACATATAC[A/G]CTATTTAAAGGAGTT	161436
rs145929925	in-del	-/TTTC	0.383824	0.211166	intron-variant	EML5	GRCh38.p7	14:88729866	CACTCGGTCTTGTTT[-/TTTC]TTTGTTTTTTTTTTT	161436
rs145931351	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756493	CTTATTAGATATTCT[A/G]GCCAAGAAAAATAGG	161436
rs145938011	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634007	CAAGTTTTTTATAGA[C/G]TAACAAGATACTTGA	161436
rs145952877	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719051	AATGTGGTAGTAACA[C/T]TGTCAGAGAGAGACA	161436
rs145987561	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698606	TTCTCAATTTCCTCA[C/T]CTGTTACTTAAATAC	161436
rs146000327	in-del	-/A	0.0486741	0.148216	intron-variant	EML5	GRCh38.p7	14:88710739	AAATAAATTACTAAC[-/A]AAAAAAGCTAACAAA	161436
rs146011825	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88694854	CATCGCTTTAATAAA[C/T]AGCAGGTTAAAATCT	161436
rs146013917	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88743353	TACATTTTTATGTAT[C/T]AAAACATCACTATGT	161436
rs146015007	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88628075	TTTGGAAAAACAGCA[C/T]TTAGACAAGCAAATC	161436
rs146024371	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88740314	AACAATATACTATAT[C/T]ACGCAGTCTATCATT	161436
rs146051947	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88772685	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	161436
rs146103206	in-del	-/TAGT	0.0887219	0.191022	intron-variant	EML5	GRCh38.p7	14:88658800	AAATGTTCAAAGTAA[-/TAGT]TAATTACAATGTATA	161436
rs146108913	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88721312	CCGTACAGCCAAGTC[A/G]ATCCTAAGCAAAAAG	161436
rs146121922	snp	A/G	0.02016	0.0983543	intron-variant	EML5	GRCh38.p7	14:88636391	CAAAAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT	161436
rs146136713	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764852	TTTTTATTTTGATTC[C/T]ATTATGGTCAGAGAA	161436
rs146147655	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88761679	CATGTGTCTTTATAG[C/T]AGAATGATTTATAAT	161436
rs146175359	snp	A/C	0.0126979	0.078662	upstream-variant-2KB	EML5	GRCh38.p7	14:88794434	CTGAAAAAGAGGAAT[A/C]GCTTTCTGGCAGCTG	161436
rs146208473	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88759121	AATCACTGAATTGTG[A/C]ACTTAAAGTGTACAT	161436
rs146230095	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88656409	ACTCATAAGTGGGAG[C/T]TGAACAATGAGAACA	161436
rs146255297	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88652433	CACCTTAACTTCATC[A/C]CTTTCCCCGAATATA	161436
rs146268926	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776843	CTGAGATTATACTGC[C/T]GCACTCCAGCATGGG	161436
rs146305209	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88788829	TTGGGAGGCGGAAGT[A/G]GGAGGATCACTTGAG	161436
rs146347580	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88678486	CACATCTGCCCTAAC[A/G]GCATAGCAGACTAGT	161436
rs146375598	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673294	CAAAGACCATATGAT[C/T]ATCTCAGTATATGCA	161436
rs146377281	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88725260	AACAATGTGAATGTA[C/G]TTAATGGCACTGAAT	161436
rs146388283	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88721546	CAATAAATGGTGCTG[A/G]GAAAACTGGCCAGCT	161436
rs146409837	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622144	TATCTTTCTGTGCCT[A/G]GCTTATTTCACTTCA	161436
rs146425623	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750971	TGTCTCCTCTGTCTG[C/G]TATAGCTCATCAAAT	161436
rs146451095	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746529	GTAGGATTGACAAAA[C/T]ATCCTAAATATACCT	161436
rs146472068	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88759684	GCAAGTCACCATCTC[A/T]TAAAAAAAAAAAAAA	161436
rs146510886	snp	C/T	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88691674	CAAGAAGCCCCATGT[C/T]AACCTCAAGCCTAAG	161436
rs146537430	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88695894	TACAACAACATGCTG[C/T]CACTAATATGACTAC	161436
rs146537509	snp	G/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88645351	TTTCTTTGGTGTACG[G/T]GTCATAATGTAAATA	161436
rs146549283	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88770112	CGCTGAAATTTGTTT[A/C]TTTTTCTCTTTTTAC	161436
rs146571412	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88736008	TTTTTTCTTTCTTTT[C/T]TTTTTTTTTTTGAGA	161436
rs146606155	in-del	-/AT	0.380919	0.21298	intron-variant	EML5	GRCh38.p7	14:88729088	ATATATAAACACATC[-/AT]ATATATATATATAAC	161436
rs146630689	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88711188	TACTTTAATTGTTAG[A/G]TATTTAGCCAGTCTT	161436
rs146642161	snp	C/T	0.0298908	0.118541	intron-variant	EML5	GRCh38.p7	14:88625687	GATTATAGGTGTGAG[C/T]CACTGTGCCCGGCCT	161436
rs146653771	snp	G/T	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88717653	CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAAAAT	161436
rs146655907	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88666454	TGGTCCTGAACTCCT[A/G]ACCTCAGGTGAACCA	161436
rs146665879	snp	A/G/T	1.68207e-05	0.00290001	synonymous-codon, stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88712292	TTAAACATGGATATC[A/G/T]GAATAATTTTATAAT	161436
rs146669025	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786586	CCCAAATCTCATCTC[A/G]AATTGTACTCCCATA	161436
rs146695268	snp	A/G	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88783168	GGGCGGAGCCCTCAT[A/G]GAGAACCTCTGCTAG	161436
rs146750036	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649139	GGCTCAAGAGACCCT[C/T]TCACCTCAGCCTCCT	161436
rs146775852	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88686204	GGAGGGGGCAGGAAG[A/G]AAGAGGAAGGACATG	161436
rs146788782	snp	A/G	0.0232847	0.105357	intron-variant	EML5	GRCh38.p7	14:88732326	ATTAAATAGGGAATC[A/G]TTTCCCCATTTCTTG	161436
rs146813406	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728190	TGCATCTGTACTGAA[C/T]ATGTACAGACTTTTT	161436
rs146897843	snp	C/T	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88774187	TACTGGGCTCTACAC[C/T]TAGAGTTTCTAATTT	161436
rs146908042	snp	C/G	0.0154538	0.0865337	intron-variant	EML5	GRCh38.p7	14:88697963	GCTGGTCTCAAACTC[C/G]CGACCTCAGGTGATC	161436
rs146919709	snp	A/G	0.0126979	0.078662	intron-variant	EML5	GRCh38.p7	14:88733909	TTTCTCTATGATACA[A/G]TCCTAGAAGTCATGA	161436
rs146982941	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88676477	CCATGATTCAATTAC[C/T]TCCCACCAGGTCCCT	161436
rs146992914	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88672047	AGCTCCGGATCAAGC[A/G]GACCTGATAGATATC	161436
rs147026053	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88753056	CCAAAAAGGCTGTCA[C/T]ACTGACTCTTCACTG	161436
rs147088195	snp	A/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88697612	CTTAATTATTCCTCT[A/T]GACTCAAGTAATCAC	161436
rs147097718	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693229	AGTATGAATACTACT[C/G]TATTAGTCTGTTCTC	161436
rs147128439	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88644200	TAGGACTCCTCTGAG[A/G]TACAGTTCAATTAGG	161436
rs147151561	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689975	GGAGTCCACTTTAAG[A/T]AGGGTGGTTAAGGTA	161436
rs147156213	in-del	-/GTGAGCT	0.373598	0.21731	intron-variant	EML5	GRCh38.p7	14:88719328	GAGTTCGAGGCTGCA[-/GTGAGCT]GTGATTGTGCTACTG	161436
rs147161293	snp	A/G	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88685409	TGTTTACCTCTTCTT[A/G]TATTAGCCCTTCCTT	161436
rs147162460	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766199	TAAACAATATGAAAT[C/T]TGGGCACCTTGAAAA	161436
rs147223043	snp	A/G	0.0150606	0.0854603	intron-variant	EML5	GRCh38.p7	14:88623991	AGGCACAAATTCTGC[A/G]CTTGTGTTTAATTAA	161436
rs147232590	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88662437	GGACGTGGCAGATAT[A/G]CAATACTCCAATCTT	161436
rs147245547	snp	C/T	0.0170251	0.090679	intron-variant	EML5	GRCh38.p7	14:88785157	CTGAACTAATGGACA[C/T]AGAGTAGAAGGATGG	161436
rs147256665	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709809	AATTGCAGCATATAC[A/T]TACAACACAATATTT	161436
rs147267213	snp	C/T	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88703005	ACCCACCTTGGCCTC[C/T]CAAAGTGCTGGGATT	161436
rs147269823	snp	A/G	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88780968	CACAGCTCACTTAAT[A/G]TTTGATTAAATCATC	161436
rs147329601	snp	G/T	0.0490535	0.14873	intron-variant	EML5	GRCh38.p7	14:88647231	TAGCCAGGCATGGTG[G/T]CACGCACCTGTAATC	161436
rs147364222	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88729922	CTTACATACTGTCTT[C/T]GTATCACACTACAGA	161436
rs147383540	snp	A/G	0.0146672	0.084371	intron-variant	EML5	GRCh38.p7	14:88644750	GAGTCTCACTCTGTC[A/G]CCCATGCTGGAGTGC	161436
rs147397000	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88769454	GAGCCAGCTAAACCT[C/T]TTTTCTTTATAAATT	161436
rs147401940	in-del	-/AACAAC	0.481242	0.0950111	intron-variant	EML5	GRCh38.p7	14:88717757	GAGACTCCGTCTCAA[-/AACAAC]AACAACAACAACAAC	161436
rs147445366	snp	A/C/G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88617844	ATACAGCCAGGAAAT[A/C/G/T]TGAACAAATTTGGAA	161436
rs147470112	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88748368	AGATACCTCTTTGAA[C/T]TCGCTGGGCAGTCAT	161436
rs147477917	snp	A/C	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88663920	GCACAATATTTAAAT[A/C]ACTTTACAAATTAAA	161436
rs147478910	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88744729	TAAACAAATGATGAA[A/C]GAAAAACTAACATTT	161436
rs147478993	snp	A/C	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88791223	TACCAGGGCTTCTTG[A/C]CTACAAGACTTCAAA	161436
rs147501816	snp	C/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88785794	CAACAGTCTCCTAAG[C/T]GGTCTCCCTGCTTCC	161436
rs147542400	snp	A/T	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88689237	TTCTCTAGGAATGCC[A/T]GGGAGTAGTAATAGG	161436
rs147573599	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88638194	ACAGGTTGGCAGATA[C/T]GTCCTAAACAGACCT	161436
rs147606356	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680907	GGAGGGAGTCAGCAG[A/G]AAAAAAACAAAAACC	161436
rs147608317	snp	A/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88763018	AAAGAAGTGTTTAGA[A/G]AGAAATTTATAGCAC	161436
rs147616187	snp	C/T	0.0490535	0.14873	intron-variant	EML5	GRCh38.p7	14:88676500	AGGTCCCTCCCACAA[C/T]ATGTAGGAATTCAAG	161436
rs147617903	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88758959	CAGAATATGCAAATC[C/T]ATAAAGAAAGTAGAT	161436
rs147677449	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658490	TAAAAATTAATCATT[G/T]CAAGTGCAATGTGTT	161436
rs147711258	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699807	GGCAACCAAGTTAAT[A/G]CACTGCTATGTTCTA	161436
rs147736275	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88684535	TTTTAGCATACATTT[A/T]TATTTTTTCTTAGAA	161436
rs147812986	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88639557	TTATATTTGTTCTTA[C/T]GTCAGTGGAGGAAGA	161436
rs147825207	snp	A/C	0.0501905	0.150254	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766337	ATAGGAGAAATATTG[A/C]TGAATTCTTTTTCTC	161436
rs147825247	snp	A/G	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88719810	TCACAAAGGAGATAG[A/G]CACATGAAAATCCCT	161436
rs147862332	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88711942	AGTGAGACCCTGTCT[-/C]AAAAAAAAAAAAAAA	161436
rs147888072	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615030	GTTGCTCCCTAAAAC[C/T]CTTACATTGTACACC	161436
rs147919424	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88685619	ACATCATTCCATATA[-/T]TTTTTTTTTTCAGTA	161436
rs147922203	snp	C/G	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88740862	TTTCTGAAAAGAAAT[C/G]TACATAAAACTTAGA	161436
rs147932025	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88782698	CAAGCCCCAAGCCTT[A/G]GCAGCTTCCACATGG	161436
rs147932528	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88736660	TAGGGGCAAGTCCCG[A/G]TGAAAGCCAACCTTC	161436
rs147942273	snp	A/G	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88653340	ACAATATGTTGAATC[A/G]AAGTAGTGAGAGACA	161436
rs147955950	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88778087	GCTTAAAATAATGGA[C/T]GATAGTATTTGCAAG	161436
rs147981909	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651680	TCATATTAAACACTA[C/T]ACTTCAAATATTCTA	161436
rs147994469	snp	A/G	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88775610	ACAACAGAACACCAG[A/G]TAGACTTCTAAGGTT	161436
rs148004969	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88698556	AGGCATGAGCCACGG[C/T]GCCCAGCTTCCTTGA	161436
rs148058903	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702076	ACATAGTCCTTTGGT[A/T]TGTCACAGGACATTT	161436
rs148069017	snp	A/G	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88747305	TAATTCCATCTACTC[A/G]GGAGGCTGAGGCAGG	161436
rs148088902	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88723700	CCAAAATCTCATGTT[A/G]TACGTCGTAAATATA	161436
rs148124724	snp	C/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88791686	TCAGTGAAGTTTTCA[C/G]CAGCCTCTTCAGATA	161436
rs148143108	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729382	CATGTCCTGTGGGCC[A/C]AACCAGGCCTGCTGC	161436
rs148195475	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694074	CACTGTGCCCAGCCA[A/G]TGTTGACATCTTATA	161436
rs148198482	in-del	-/G	0.0279526	0.114869	intron-variant	EML5	GRCh38.p7	14:88688573	GTTGTTGTTTGAATA[-/G]TAAGGCATGCAACAG	161436
rs148214166	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622491	TGTTGGCAAGCAAAT[C/T]CATCGTTATGCATTA	161436
rs148220211	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88739852	CCAATTAATAGAAAT[A/G]TAATGCACTGAGGAC	161436
rs148269906	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88662225	CTTATGGTCTCTCCC[C/T]TCATTAAGACACTTT	161436
rs148282706	in-del	-/TG/TGTTTGTGTGTG/TGTTTGTTTG			intron-variant	EML5	GRCh38.p7	14:88745167	TCTAAATTGTGTGTT[-/TG/TGTTTGTGTGTG/TGTTTGTTTG]TGTGTGTGTGTGTGT	161436
rs148282993	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784307	AGGGCAGAAATAAAT[G/T]ACATTGACATTTTAA	161436
rs148289296	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88634632	CTGTAAGAGAAGGCA[C/T]TCATTTCAATCATAC	161436
rs148302864	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763821	TCTTTTTCCTGCTTT[C/T]ACAAGGAAAACATTC	161436
rs148343727	snp	G/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88643573	ATTTTGGCATCCCCA[G/T]GGGGAATCTATCCCC	161436
rs148353591	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88688958	TTTTAAGCAATCTCA[C/T]TTTTCATGTTTTAAA	161436
rs148355367	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767319	CCTGATATGCAGGCA[C/G]TTCCTGCACATGCAG	161436
rs148435982	snp	C/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88644789	AATCTTGGCTCACTG[C/G]AACCTCTGCCTCCTG	161436
rs148449442	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88769529	ATACAGGTGTTTAGA[A/G]AAAAGACAATATCTA	161436
rs148459038	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691594	GAATAGAGTTCAAAT[C/G]CCTTAGGGGAGAGAT	161436
rs148511544	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88652843	TCTTAATCTGTCATC[C/T]AGCTCAGAGACTTTA	161436
rs148523758	snp	C/T	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88777437	AAATGCTAAAGGAAG[C/T]ACTTCAATCAGAAAG	161436
rs148533727	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88668731	GCAGGCATAAAGCAG[A/G]TAGAAAGTTGAGTTT	161436
rs148542806	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88717462	TGATTTGGTTCCAAC[A/G]TAAAAAACAAATAAG	161436
rs148593216	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88637297	TCTGTACTCCCCAGA[G/T]TTTGACTTGGAAAGA	161436
rs148595239	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88721724	CAAAGATTTCATGAA[G/T]AAATCGCTAAAAGCA	161436
rs148598225	in-del	-/TTGT			intron-variant	EML5	GRCh38.p7	14:88760343	TAATGTAGGTTATAG[-/TTGT]TTGTTTGTTTGTTTG	161436
rs148664525	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613721	CAGAGGGCACAGTGT[G/T]CTTTGGCATGCATTT	161436
rs148668807	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648799	TGTGAGGCTAGATCC[A/G]GGTGCTTTATTTCTG	161436
rs148669342	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731110	GTTCTAGGGTACATG[C/T]GTACAATGTGCAGGT	161436
rs148679466	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88772546	GATCACGAGGTCAGG[A/G]GTTCAAGACCAGACT	161436
rs148723377	snp	C/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88697167	TGTTTCCAGGAATGA[C/T]GTAACTAACACTATG	161436
rs148732670	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88740731	CAGATTCTCATCCTA[C/G]TGCTGTCAAAAGCTA	161436
rs148741803	snp	C/T	0.0322114	0.122752	intron-variant	EML5	GRCh38.p7	14:88624312	ACTCCTGGGCTCAAG[C/T]GATCCACCTGCCTCA	161436
rs148751892	snp	A/G	0.345925	0.230864	intron-variant	EML5	GRCh38.p7	14:88672865	TCCCTGAATAGACCA[A/G]TAACAGTTCTGAAAT	161436
rs148752912	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88755559	ACATCAGCAGAAGGC[A/G]GGGAAAATATAAATT	161436
rs148787125	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88745530	TTAGGTCTCTAAAAA[A/T]TGTAATAGTAATACG	161436
rs148804733	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88678955	GAGCTATGCTCCGTT[C/G]TGAAAGTTCTTGGGA	161436
rs148809981	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88786289	CAAACTATACATATA[C/T]ACATGCATATATAAA	161436
rs148836969	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88742255	GATGATGAAAATATT[-/AC]ACACACACACACGCT	161436
rs148838566	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627434	TATAATGCTAATAAT[C/G]GTTTCATTAATTTAT	161436
rs148839015	snp	A/C/T	8.6265e-05	0.00656707	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712447	GAAGCCCAATGAACA[A/C/T]CTTTTATTTCTTCTG	161436
rs148841695	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88741690	GCTACTGCACTCCAG[C/T]ATGGGCCACATGGTA	161436
rs148862087	snp	A/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88758319	TGCCTCAGTCTCCCA[A/G]GTAGCTGGGATTACA	161436
rs148890236	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634556	AAAACCCAAATATCA[C/T]ATTAATTATAATTTA	161436
rs148904646	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88788823	AACACTTTGGGAGGC[A/G]GAAGTGGGAGGATCA	161436
rs148912831	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88681153	CAAAATTAACTAATG[G/T]GTAGCTTAAAAAACA	161436
rs148915600	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88763662	CCCATTTTATGAGGC[C/T]GGCATCATCCTGATA	161436
rs148966428	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88646113	ACCTAAATCAGGAAA[C/T]AATACAAATTAACCT	161436
rs148977792	snp	G/T	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88770766	AGTAAAAACTCAACA[G/T]TTATGGATTAATTTG	161436
rs148994998	snp	A/C	0.0185938	0.0946107	intron-variant	EML5	GRCh38.p7	14:88704357	CTTCACCAGAAGCTG[A/C]GCAGATGCTGGTGCC	161436
rs149028423	snp	C/T	0.00752712	0.0608843	intron-variant	EML5	GRCh38.p7	14:88739041	AATAAAATAATTTAA[C/T]GACAAATATTTTTTA	161436
rs149046598	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88671461	AAACACACTGAAGTA[C/T]GAAAATCAATGATAC	161436
rs149051334	snp	C/G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88778913	CTTCTTTGTGGTTGG[C/G/T]TGGAACAATGTTATT	161436
rs149055297	in-del	-/TT	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88637129	AACAAAACAATTCTC[-/TT]TATGTGTGAGGAGAA	161436
rs149070631	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88719015	AGCAAAAACTGTCAC[A/G]ATCCCTTTTAAAGTT	161436
rs149120955	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88641216	ATCCTACTGAAACTA[C/T]TCTAAAAAATAGAGG	161436
rs149124111	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88723474	ATGGGGAGATGTTGG[C/T]TAAAGAGTACCAAGT	161436
rs149177501	snp	C/T	3.31219e-05	0.00406938	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688306	TGAACACTGGCCCAT[C/T]ATGCGCTTTCACTGT	161436
rs149185919	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88732675	CATTTTCAGTTCTGT[G/T]AATTTTTGCCAGATA	161436
rs149196497	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615656	CAGTGCATATAGCAA[A/G]TATTTTGAACAGATC	161436
rs149238950	snp	C/T	0.0154538	0.0865337	intron-variant	EML5	GRCh38.p7	14:88698083	AACACTGCAATCAGC[C/T]AATATTTCACTAAGT	161436
rs149251333	snp	C/T	0.0107246	0.0724382	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612690	ATTTAAATAGTATAT[C/T]TTAAATGACAGAACT	161436
rs149295969	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735159	ACTTTTGAGTATATC[A/G]TAGTCACTTGGAAGG	161436
rs149303369	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88617436	ACAGGCTGAGCCACC[A/G]CGCCTGACTGAAAAC	161436
rs149312972	snp	A/C	0.0205511	0.0992634	intron-variant	EML5	GRCh38.p7	14:88668018	TGGCAAGCTTTTTCG[A/C]CACAAGCTCACTGAA	161436
rs149315948	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88747140	AAAAAGGGTCAGGTG[C/T]GGTGGCTCACACTGT	161436
rs149329935	in-del	-/T	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88648872	CATACTCTGAACTCA[-/T]TATCTTTGTACACAC	161436
rs149365587	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88629429	TAAGGTAATGGAATT[C/G]TCACACACTTAGACT	161436
rs149369776	in-del	-/GAA	0.3752	0.216391	intron-variant	EML5	GRCh38.p7	14:88624858	GAAGCATATGAGGAG[-/GAA]GAAGGTCGGAGAGGA	161436
rs149379373	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88760925	TTGTAGACAGTATTG[C/T]TGTAAAATTTCAGTT	161436
rs149431863	snp	A/G	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88684104	CTAATAAATGAGGAC[A/G]GCAAGTTTACAGGTT	161436
rs149433959	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765896	TCAGGGACCCCGAAC[G/T]GAGGGACCGGCTGAA	161436
rs149451907	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88654328	TCTACTAGCTTTTGA[A/G]TTTGTTTGCTCTTGC	161436
rs149503683	snp	C/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88661452	TGAAAAACACTATAG[C/G]ATATGATATATAACT	161436
rs149508632	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772483	ATACCTTCGGCCGGA[A/C]GAGGTAGCTCATGCC	161436
rs149528239	snp	A/G	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88707343	ATGTTGCCCAGGCTG[A/G]TCTCGAACTCCTGGG	161436
rs149529610	snp	A/G	0.100588	0.200439	intron-variant	EML5	GRCh38.p7	14:88784021	GGAATACAAATACGT[A/G]GAAATTAAACAATAT	161436
rs149571202	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88780909	ATAATCTCCTTTCCT[A/G]AAAGCCAACTGATAA	161436
rs149588857	snp	A/G	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88720882	CTAGAAAACTCCATC[A/G]TCTCAGCCCAAAAGC	161436
rs149641449	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88725718	AAGGTCTTGAGGGAA[A/G]CCAAACAGGAGGTAA	161436
rs149653094	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88644173	AAAAGATCATTCACA[C/T]ATACTTAGGTTTAGG	161436
rs149662277	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626691	TGAAAGAACTAGATT[G/T]TTGAAAGATGAAATA	161436
rs149674804	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88757689	TACCCCCAAGGAAGA[C/T]ATACAAAAGGCACAT	161436
rs149685212	snp	A/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88676077	TTCTTACATTTTCCT[A/G]TCTGCTTCTGAGCCC	161436
rs149692787	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690777	CAGTAGAGAAAGGGT[A/G]GAAGAGTTAGAGTGA	161436
rs149702618	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88735999	ATCGGAGTATTTTTT[-/C]TTTCTTTTTTTTTTT	161436
rs149727238	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88681052	AAGATAGAAAAGAGT[A/G]AATCTAAAATATAAA	161436
rs149748832	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88727262	TCACCATATGGTAAT[A/G]CACATAGCGGTCAAA	161436
rs149780963	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88729863	ACCACACTCGGTCTT[G/T]TTTTTTGTTTTTTTT	161436
rs149821310	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88620076	CTTACTGAGGTACGA[C/T]AGAGACATGTAAAAG	161436
rs149822805	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703392	TTTTATACACATTGT[A/T]GGACCATGAGAATAC	161436
rs149832682	snp	G/T	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88750160	ATCAAATGGTGGTTT[G/T]GAGCACAGATTCTGG	161436
rs149834190	in-del	-/TC	0.0329836	0.124112	intron-variant	EML5	GRCh38.p7	14:88779502	AGAAAATGAGTTGGT[-/TC]TCTGTCATCTTTAGA	161436
rs149854728	in-del	-/AATA	0.0221141	0.102801	intron-variant	EML5	GRCh38.p7	14:88697694	ACTCCTGAAATAATT[-/AATA]GAGCTGTCAATTATA	161436
rs149886554	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88717923	CATACTATTATAGGA[C/T]GTAATACGTACTATA	161436
rs149897630	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88633030	TTCAATGTAATAAAC[C/T]AAAGCCTTAAGTACC	161436
rs149916770	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88648740	ATAAACTATCCAAGT[C/T]TCCTTTAAAATGTAG	161436
rs149959061	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88652535	AAAATTCTTCAGCAC[C/T]ATCCTAAATGGCCAC	161436
rs149978940	snp	A/G	0.00591486	0.0540596	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658320	CAACATGCTGTCATC[A/G]TAAGTCCAGCGAACA	161436
rs149982514	snp	C/T	0.000109397	0.00739504	intron-variant	EML5	GRCh38.p7	14:88740615	ACCAAAGAATTCTTA[C/T]AAAATAAAGTAAAAC	161436
rs150026752	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88623034	TTTTTTTTTTTTTTT[A/T]AGATGTAGTCTCGCT	161436
rs150028102	snp	A/G	0.376989	0.215346	intron-variant	EML5	GRCh38.p7	14:88654097	GCATTCTCTGATGGT[A/G]GTTTGTATTTCTGTG	161436
rs150042908	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88710917	ATTGTGCAATAATAT[C/T]GACTTCTCTCTTGCA	161436
rs150045109	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786231	CTAAACTCTTCCCAA[C/T]AGTTTCTATCGCATT	161436
rs150070359	in-del	-/AACAAC	0.0197687	0.0974348	intron-variant	EML5	GRCh38.p7	14:88674273	AGACTTCATCTCAAA[-/AACAAC]AACAACAACAACAAT	161436
rs150075895	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88741290	TGATAGAAACATTAA[A/G]GATAGGAAAAAAAGA	161436
rs150082230	in-del	-/TTGTA	0.00159617	0.0282053	intron-variant, utr-variant-3-prime, frameshift-variant	EML5	GRCh38.p7	14:88616080	AAGCTGTAGGAGTTG[-/TTGTA]TTAAGTCTCTTAACT	161436
rs150087226	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660517	GGAGGTCGAAGTGGG[C/T]GGATCACAAGGTCAG	161436
rs150097637	in-del	-/TTG	0.499992	0.00199679	intron-variant	EML5	GRCh38.p7	14:88780382	GCACAAAGGGTAGAT[-/TTG]TTTACTGTTCAGTAT	161436
rs150099287	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88783130	AGAAAATGCCTGGAC[A/G]TCCAGGTAGAGGTAT	161436
rs150139121	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88667694	ACTCCCTTCCTCCAG[C/T]GTGCTGTTTTACTAA	161436
rs150152347	snp	C/G	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88788774	AAAAGATATTGCACT[C/G]TGGCTGCACACGGTG	161436
rs150202813	snp	C/T	0.0980852	0.198549	intron-variant	EML5	GRCh38.p7	14:88677327	TTAAAGACTTAAATG[C/T]AAAACCCAAAACTAT	161436
rs150204007	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760790	TCCAATCCATAAACA[C/T]AGTACGCCCGCCCTC	161436
rs150223619	snp	A/C	0.0494327	0.149241	intron-variant	EML5	GRCh38.p7	14:88692342	AGATCACAACATTGC[A/C]CTCCAGCCTGGGCAA	161436
rs150274346	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612183	TTTTCCCAAAGATTA[C/T]ATAATGTTCATAATC	161436
rs150276969	snp	G/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88729685	GTGCCTCACCCTCCT[G/T]AGTAGCTGGGATTAC	161436
rs150285808	snp	A/G	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88778519	GGTGTGGTGGCTCAC[A/G]CCAGTAATCCTAGAA	161436
rs150289241	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88759685	CAAGTCACCATCTCT[A/T]AAAAAAAAAAAAAAA	161436
rs150296448	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700656	TTTTTAATCACATCT[C/G]TCTACCTGAAAACTC	161436
rs150336929	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88706072	ATCAAAATTACTTTG[C/T]ATTTCACACTCTGTG	161436
rs150360200	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88752240	GCAATATATTACATT[C/T]AGAAAGGGCAAATTT	161436
rs150368190	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640213	TGACCAATTGGACAT[A/C]ACAGAAAGAACACTC	161436
rs150413072	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88720711	TTGCCCTTGAAAACT[A/G]GCACAAGACAAGGAT	161436
rs150423348	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88764031	TAGCAATTATATAGC[A/G]AATTACACTGATTAA	161436
rs150432310	snp	C/T	0.0310518	0.120672	intron-variant	EML5	GRCh38.p7	14:88650190	GGGCAAGGTGGCTCA[C/T]GCCTGTAATCCCAGC	161436
rs150433760	snp	G/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88732540	CTTAGGATTGTCTTG[G/T]CAATGTGGGCCCTTT	161436
rs150482128	snp	C/T	0.0102534	0.0708631	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644457	TCTCTTTTTCTTGCC[C/T]ACATTGTTTGTCTGG	161436
rs150485344	snp	C/T	0.0115144	0.0749975	intron-variant	EML5	GRCh38.p7	14:88653512	TAGCATGAAGGGGTG[C/T]TGAATTTTATCGAAG	161436
rs150522500	snp	C/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88722371	AATCCACCCAAATGC[C/G]CATCAATGATAGACT	161436
rs150529684	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734786	CTATGTTAAAATACA[A/C]TATGGGTATGCAATT	161436
rs150552722	snp	G/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88776234	CTAGCATCAACACCA[G/T]CCAAGAAAACATGAC	161436
rs150594054	snp	A/G	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88657570	GATCTTATAAATTGG[A/G]TACAAAGATGTTCAA	161436
rs150594628	in-del	-/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88717166	TGTCTCCATTTTGTT[-/C]TGAGGAATGAATGAG	161436
rs150605912	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88744220	AATAATAATCAACAT[C/G]CCACACTTCAAAATC	161436
rs150613682	snp	A/C	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88629143	TGATAAATATTATAT[A/C]AATATTTTTATATGT	161436
rs150647434	snp	C/T	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88618922	CGTGTGATAAGGCCT[C/T]AAATAGATTTACCTG	161436
rs150657144	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88669537	CTGTGCGGGGCCTCC[C/T]TGCAGGAATTTCAGC	161436
rs150667875	snp	A/G	0.00358779	0.0422022	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791986	AGGATCTAACGGAAT[A/G]AAGTGCCACCAAAAT	161436
rs150675877	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88683179	AAAAGTAATTGGGAG[A/G]AGACTGGTAGGCTAA	161436
rs150703698	in-del	-/GCACCAGTTAGAA	0.403334	0.197456	intron-variant	EML5	GRCh38.p7	14:88728322	TGACCCTTGAATAAT[-/GCACCAGTTAGAA]GCACCAATTCCCATG	161436
rs150719213	snp	A/C	0.0134861	0.0810011	intron-variant	EML5	GRCh38.p7	14:88762328	CTAGCCTGACCAACA[A/C]AGAGAAACCCAGTCT	161436
rs150740881	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88772275	ACATCACAACTACTT[C/T]GGTAGCCTTCTGTCT	161436
rs150750550	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694246	CTGCACTTAGCTAAA[C/T]TACTTTCAAAAGCAA	161436
rs150792678	snp	G/T	0.0162398	0.0886349	intron-variant	EML5	GRCh38.p7	14:88698813	ATCTCACCTGGAAAT[G/T]ATGATGATGACTAAC	161436
rs150814616	snp	G/T	0.000137334	0.00828543	intron-variant	EML5	GRCh38.p7	14:88702665	TCATATATAATTAAT[G/T]TTGGCCTTTTATCTG	161436
rs150815805	snp	C/T	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88780636	GCTGGAGTGCAGAGG[C/T]GCGATCTTGGCTCAC	161436
rs150868747	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88710409	GTCACCTAATGAATA[C/T]TACCTGAGTGGATAT	161436
rs150887956	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643926	TTTGGTTGTTCGCTA[C/T]TGCTACCGGGATTAT	161436
rs150890726	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755787	CACCTGAGGTCAGGA[A/G]TTCAAGATCACCCTG	161436
rs150920441	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88674591	GAATTCGAGATGAGA[C/T]TTGGGTGGGGACACA	161436
rs150923760	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705213	ATTTTTATACTTCAT[A/T]AAAGAATATTGTTAA	161436
rs150994480	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88645012	AGTGAGCCACCACAC[C/T]CAGCCTTTTCTCTTC	161436
rs151007558	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770016	AAGATACTGTTAAGA[C/T]ACTGTTTTTCAGTCA	161436
rs151056928	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88652906	TATGGCCATTTTCAC[A/G]ATATTGATTTTTTCC	161436
rs151070242	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88777487	ATAAGTAATCCCAAG[C/T]GGGTTTTGAAGGTAC	161436
rs151078449	in-del	-/A	0.0448719	0.142907	intron-variant	EML5	GRCh38.p7	14:88788183	AACCCATATAAACAC[-/A]AAAAAAAATCTATCT	161436
rs151112346	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660244	GCCATGATTGCGCCA[C/T]TGCATTCCAGCCTGG	161436
rs151123594	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783012	TGAACCCAAGAGCTG[A/G]AGGTTGCAGTAAGCC	161436
rs151132710	snp	C/T	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88632389	CTCAAAGTATAAATT[C/T]GGTCATATCACTCCC	161436
rs151135803	snp	A/G	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88745931	ACCCCAGAACTTAAA[A/G]GTATAATAAAAAAAA	161436
rs151143949	in-del	-/TTTCAC	0.368119	0.220336	intron-variant	EML5	GRCh38.p7	14:88645054	CTTTTTTAGACCAAG[-/TTTCAC]TTTGTCACCCAGGCT	161436
rs151155697	snp	A/G	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88679553	AAAAATAAGCCAGCC[A/G]TGGTGGCGCACGCCT	161436
rs151176067	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751351	ACAGTTTGTAGAAAA[C/G]TAATAGTACATTTCA	161436
rs151186528	snp	A/G	0.0490535	0.14873	intron-variant	EML5	GRCh38.p7	14:88672011	ACAGAAAATTAACAA[A/G]GATATTCAGGACTTG	161436
rs151207257	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685641	TTTTCAGTAGGGTGG[C/G]GTTGTGCCATTTTGC	161436
rs151261129	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88649737	TTATAATAACAACCA[C/T]ATATGCTATCTAAAA	161436
rs151320955	snp	A/C	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615905	ATGTTTTTAGATTTT[A/C]ATAACAGTTTAATAT	161436
rs151322404	snp	A/G	0.0414363	0.137845	intron-variant	EML5	GRCh38.p7	14:88700495	AAAGCATCAAAACAC[A/G]AAGGAAAAATTTCCA	161436
rs180680947	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623422	CTATGCTACAGAGTT[G/T]ATTTATTTATTTTTT	161436
rs180687548	snp	C/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88645486	CTAAAGTATCTAACA[C/G]AGTATCTTCACATGG	161436
rs180690568	snp	C/T			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614435	GTAATTTAGTCATTT[C/T]TATTTTTAGTATTAA	161436
rs180699513	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88665557	ATGGGCCAGGTGTGG[C/T]GGCTCATGCCTATAA	161436
rs180703050	snp	C/G	0.000182302	0.00954556	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658264	CCTTCCATCTCATTT[C/G]TCCACACCATTAAAG	161436
rs180707080	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689459	TTTGCATTTCTGTGA[A/C]TATTATGCTAGATCA	161436
rs180709243	snp	A/C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88678278	GGAACACACACTGGG[A/C/G]CCTCTTGGGGGACAG	161436
rs180716818	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88635922	GCCATCTGCAAATAC[A/G]GAGAAGGCCCTCACC	161436
rs180783741	snp	C/T	0.00993419	0.0697739	intron-variant	EML5	GRCh38.p7	14:88777754	GCTGAGGCAGGCAGA[C/T]TGCTTGAGCCCAGGA	161436
rs180785256	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88761609	CATTGATGGGCATTT[C/G]GGTTGGTTCCAAGTC	161436
rs180793396	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740681	GCTAAAAATTAACTA[A/T]GAAATTGCCTTATGA	161436
rs180800944	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717454	CAAATCACTGATTTG[C/G]TTCCAACGTAAAAAA	161436
rs180805280	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88749369	GAGTCAAAACAAAGT[A/C]TTTTTCAAGCAAACA	161436
rs180822675	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767160	CAGACAAGCAATCCA[A/G]TTAGGTTCAAGGTAC	161436
rs180842267	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698635	ACAAACCTCTCCCAA[G/T]GTGGTCTTTAATTCT	161436
rs180844386	snp	A/C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88728963	TTTTATAGTATTTTT[A/C/T]AAATTGTTACTAGTT	161436
rs180959754	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682496	TACTCAAGAAAATCT[A/G]TTAAAATTTGTTAAG	161436
rs180970191	snp	A/T	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88702088	GGTTTGTCACAGGAC[A/T]TTTGTTAAATAATTT	161436
rs180972741	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652984	TTTCCTTGAGCAGTG[A/G]TTTGTACCTCTCTTT	161436
rs180979121	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672683	AGAATCAAATCGACA[C/T]AATAAAAAATGATAA	161436
rs180994272	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694728	AACAATACTTTGTTA[C/T]AGCTTAAGATAGCCT	161436
rs181007820	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782080	ATGTGGGAAAGTCTG[C/T]AAGTTCCTAGAGACT	161436
rs181027457	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713017	TTTTGGGGAGATGCA[C/T]TAATTGAATTATGCA	161436
rs181031790	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734708	ATATCCTGAAAATTC[A/G]TAACTGTATCTCATC	161436
rs181046862	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764226	TTTCTTCAAATGTTT[A/G]TCTGGATTTTGTATT	161436
rs181050738	snp	A/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88745502	TATTCTAACAAGTCA[A/T]CAGTTAAAAATGTTA	161436
rs181053098	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88617771	TATGCCTGGCTGATA[C/G]AGGAATTTGATGGCA	161436
rs181070602	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88661112	CTCTCTCTCTGACAC[A/G]GGGTTTTGCGCTGTC	161436
rs181074159	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88628871	TTAAGTAGAAATTGT[A/T]CAAAGATTTATGCAA	161436
rs181074284	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88640419	AAACCACACAATTAC[A/G]TAAAAATTAAATAAC	161436
rs181112576	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794380	TACATAGATGTCATG[A/G]AAAGTAAACTCTGAA	161436
rs181133143	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88773101	CTATGTTTTACTTGA[C/T]CTTTTAACAATCCAG	161436
rs181133879	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88755990	CACTGCATTCCAGCC[G/T]GGGCTTCTGGGCCAG	161436
rs181204231	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88708149	TTGTAAAATAAGTCT[A/G]AGAGAAACCAGTATT	161436
rs181213097	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613623	ACATTTGTTGGATGA[C/T]GTGGTTTAAAATGAT	161436
rs181252934	snp	C/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88787294	GCTCATTGAGCATCT[C/G]ATTGTGTCTAAACTC	161436
rs181261432	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751603	CTACAGAACATTCAA[C/G]TGTGATATTTAGAGT	161436
rs181268150	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88729548	GGAAGTATAGGCATA[C/T]ACTTATTTGGTTTTT	161436
rs181289026	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88716916	CTATTAGATGAAAAT[C/T]TGTTAATTTTTTAAA	161436
rs181322785	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88635354	GGAAATATCATTTTT[A/C]GTTATGAATATGCTC	161436
rs181324424	snp	A/G	0.000345752	0.0131437	intron-variant	EML5	GRCh38.p7	14:88657337	CCATTTTTAATGACA[A/G]TATCTTTTTCTTCAT	161436
rs181334928	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677931	TTTGACCCAGCAATG[A/T]AATTACTGAGTATAT	161436
rs181347674	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647434	GGGCACAGTGGCTCA[C/T]ACCTGTAATCCTAGC	161436
rs181354965	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690631	AGGTGGTTTAGCATA[A/G]AAGATGACAAATTGA	161436
rs181357338	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88761247	GAGATACATGTGCAG[A/G]ACGTGCAGGTTTGTT	161436
rs181374587	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738507	TGAACAAAAGTTTCC[C/T]AACCCTCAATATTTA	161436
rs181458462	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88793536	GTACCACTATGCCCG[A/G]CAAATGTTTTGCTTT	161436
rs181470734	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725805	ACAAGAGTACAATGG[C/T]GAGAATAGAAGGAAG	161436
rs181471000	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88698032	GTGAGCTACCGCACC[C/T]GGCCGAGATTGATTT	161436
rs181471817	snp	A/G	0.00953873	0.0683987	intron-variant	EML5	GRCh38.p7	14:88772686	TGAACCTGGGAGGCG[A/G]AGGTTGCAGTGAGCC	161436
rs181475126	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88777452	CACTTCAATCAGAAA[C/G]AAAAGGACATTAATG	161436
rs181475944	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755658	TCACACCTGGCATCA[A/C]GGTGGAGAATCACTA	161436
rs181485011	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734006	CTAAAACAACCTACA[C/T]GAAGTAAAAAAAAAA	161436
rs181490058	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88628063	CCAAATTGCACTTTT[A/G]GAAAAACAGCATTTA	161436
rs181498889	snp	A/G	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88672515	GAGCAAACAAACCCC[A/G]AAGCTAGCAGAAGAC	161436
rs181537466	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88704162	ATCCCTCATGAATGG[C/T]TTGGTGCCATCCCCT	161436
rs181618167	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666145	AAAAAGCCAATGATA[C/T]ATGTGGAAGTTTTGC	161436
rs181622541	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652459	ATATAAAATCCATAG[A/G]TGCAAACTCAAATCC	161436
rs181632681	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689711	TACGCTCCAGCCTGC[A/G]TGACAGAGCAAAACC	161436
rs181638440	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707868	AGGGCTTTGGCTACT[A/G]CTACTACCTTTGATG	161436
rs181639493	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88693848	AGATCACAGCTCACT[A/G]CAGCCTTAACCTCCT	161436
rs181644480	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88746980	TCAAAGTAGTCTTCA[A/G]GGTTGGCTGTGTCTT	161436
rs181681356	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88729092	TATAAACACATCATA[C/T]ATATATATAACCAAC	161436
rs181689666	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88712058	GTGCATTCATAACAA[A/C]ATATGAATTCAAAAA	161436
rs181708478	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88765230	AGTCCTGTGCATACA[C/G]TCTCACAAGGCCAAA	161436
rs181714239	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623692	GTTGGGATTACAGGC[A/G]TGAGCCACTGCAACT	161436
rs181716847	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646851	ACTGTGAAGAGAGGT[A/G]AAGAACACTAAGTAA	161436
rs181722142	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783364	TAGAGTAGGTGAATG[G/T]ATGAACAGATCAATG	161436
rs181793660	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778089	TTAAAATAATGGATG[A/T]TAGTATTTGCAAGTC	161436
rs181798596	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88762403	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	161436
rs181831802	snp	C/T	0.00399379	0.0445078	intron-variant	EML5	GRCh38.p7	14:88627076	CAAAATTATCTAGGT[C/T]ATTACAAGAACCAAG	161436
rs181834700	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88651676	TAAGTCATATTAAAC[A/C]CTACACTTCAAATAT	161436
rs181872855	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767631	TTTTGCATATGTGTG[C/T]CTGCTTGTGGCCTAC	161436
rs181886852	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613007	AAAGTTCATTGACTT[A/G]CTTAGTCGTATACTC	161436
rs181915340	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88671565	AATATTAACCTTAAA[A/T]GTAAATTGGCTAAAT	161436
rs181924894	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88693004	TGGAATTTATAAGTA[A/T]ACTATTTAGAAAACA	161436
rs181943586	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88711328	CCCCATGCTGTTTTC[A/G]TGACAGTGAGTGAGT	161436
rs181975306	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88782786	ATTTCAGAGAATGTA[C/T]GAAAATGCCTGGATC	161436
rs182123832	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725586	GGGCACTACATACCA[C/T]GTGAAGGATTATGAG	161436
rs182144328	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88750041	GTGCATTGTCTATGA[C/T]TGCTTTCACACTGCA	161436
rs182163258	snp	C/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88633434	CATCTCATTTGATTA[C/T]AATACAATCCATGCT	161436
rs182176596	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88780573	ATGTTTATAAAAAAT[A/C]TTTTTTTTTTTCTTT	161436
rs182186693	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763438	TAGACACACACACCC[C/T]CCCAAGACTAAACCA	161436
rs182187328	snp	A/G	0.0126979	0.078662	intron-variant	EML5	GRCh38.p7	14:88641000	AAAAAGAAGAAGAAG[A/G]AGAAGAAAAATCTAG	161436
rs182194630	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88743233	TGAGTATAGGTAATA[C/T]GAATACACAGTTTCA	161436
rs182196946	snp	A/C	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88680922	AAAAAAAACAAAAAC[A/C]AAAACAAAAAAACAA	161436
rs182199900	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721077	AAGAGAAGTGAAAGA[C/T]CTCTTTAAGGAGAAC	161436
rs182202309	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700078	TCTCTGTGTTTCCCC[A/G]CAACATTTAATGCTT	161436
rs182207349	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88683907	AGGAACAAGACAAGG[A/G]TGTTCTGTTCTCACC	161436
rs182210275	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764677	GATTACTGACCTGAG[A/G]TTATTTTTCTTTTAA	161436
rs182227710	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88786903	CTAATGAACCAACTA[C/T]GTCAAATCATGATGA	161436
rs182252345	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88649343	TACAGGCCTGAGCCA[C/G]CGTGCCCAGCCATGA	161436
rs182379957	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784099	AAAAATTTCTTGAAA[C/G]AAATGTAAGTGGAAA	161436
rs182381405	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765613	ATATCTTAAGGTACA[C/T]CCCTATCTTAATTAT	161436
rs182390713	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88747281	GCCAGGCGTGGTGAC[C/T]CACGCCTGTAATTCC	161436
rs182395008	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726488	GAGAAAATTACTTAT[A/G]TTCTGTATCACTGAA	161436
rs182403114	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88704321	CCTTTGCCTTCTGCC[A/G]TGAGTAAAAGCTTCT	161436
rs182410661	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675802	ACCAAAGTCACCTCA[A/G]GAATAATTTGTTGCT	161436
rs182414542	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88696688	AGCTAGCAAATCCAC[A/C]CTTTCATAGTATTTG	161436
rs182448889	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88619239	GCATGGTGGTGCACG[C/T]CTGTAATCCCATCTA	161436
rs182457196	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88662456	TACTCCAATCTTAGA[C/T]GGCATGTCTTCTATT	161436
rs182471136	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752253	TTTAGAAAGGGCAAA[C/T]TTAAAGCTAAGAAGA	161436
rs182478310	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703315	TAACAGTAACTATCT[G/T]CAGAGAGGGGAAATG	161436
rs182481272	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88746084	TTAATTACATATGAC[C/T]TATCTGGCAATAACA	161436
rs182529839	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659313	GCCTCCTGGTTCAAG[C/T]GATTCTTCTACCTCA	161436
rs182532499	snp	A/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679896	ATAGTATAGTGTAGC[A/G]TATAGTAAGGGCCTT	161436
rs182541536	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88699460	TCCAACCTCCCCTTT[C/T]TATCTCTTATCATTT	161436
rs182542904	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667364	ATATTCCTTGTGTTA[A/G]AAGAATATAAGACCG	161436
rs182546742	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638034	ATATTAAAAGTATAA[A/G]TTATCTTAGTCAAGA	161436
rs182556244	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88709459	GAACCCATGTTTGAC[A/G]GAGGAGAAAACACAG	161436
rs182560372	snp	A/C	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88788185	ACCCATATAAACACA[A/C]AAAAAATCTATCTAC	161436
rs182595866	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615331	TTTGCCTTTTAAAAA[C/T]TGTGATCCTTTAGGA	161436
rs182610380	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637431	GACATTTCTTAACTA[A/C]GAAAGAAAACCACAG	161436
rs182692650	snp	C/T	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621260	ATTTTTCTCTCCAAC[C/T]TCGATTATTTCAGCA	161436
rs182705752	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663528	TTTAAAATACTTAAC[A/T]TTTATCAAACATATT	161436
rs182736296	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619961	TGAGCCACCGCGCCC[A/G]GCCTGAAGAACTTAT	161436
rs182738556	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729913	TGTCTATGGCTTACA[C/T]ACTGTCTTTGTATCA	161436
rs182750744	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642713	TATACTCTCTTAAAA[C/G]TGAAATTTGTTTACT	161436
rs182787037	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789787	TCAGCCTTTACCACC[A/G]ACATTGCACTCACAT	161436
rs182790400	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88736531	TCCAACTAGAATGTG[A/G]TCACCTCGCCAACAC	161436
rs182797699	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770305	TTATAATTTTACTTT[C/T]TATAATTCATGCTTT	161436
rs182799382	snp	A/C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753826	ATTTTAATAGACAAC[A/C/G]TTTAAGGTAACTGAA	161436
rs182817597	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617177	TTGAGACGGAGTTTT[C/T]GCTCTTGTTACCCAG	161436
rs182823473	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690702	ACTTATTTAAGATGG[C/T]GAAATCACATCACAC	161436
rs182830246	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659942	TCTTTATGTTCATGT[C/T]GGTGCCAGAGTATAA	161436
rs182841893	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88768878	TTTTCTGGAAAGGGC[C/T]AGAGAGTAAATGTTT	161436
rs182849158	snp	C/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88663114	TGTTGACCTGTAAAA[C/G]CTTTCCTTCAAAAAA	161436
rs182854734	snp	C/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88684708	TGATAAGAAATTACT[C/G]AAAATATTGGCAATT	161436
rs182867906	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88774348	TAACCAAGTAAAGCA[G/T]AAACTGCTGGAACAA	161436
rs182968609	snp	G/T	0.000576076	0.0169619	intron-variant	EML5	GRCh38.p7	14:88643058	CCATTATATTCTTCC[G/T]CATGTATAAATGTTC	161436
rs182994171	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88685488	ATTCAATTCAAGATA[C/T]ATAGTCAGCCCTCAG	161436
rs183019443	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774231	TGAGCCCAGATAATT[C/T]GTATTTTTTAGTAAC	161436
rs183031654	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757893	TCTCACTCTGTCACC[C/G]AGGCTGGAGTACAGT	161436
rs183057541	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762913	GCTCCTGAGTGACTA[C/T]TGGGTAAATAACAAA	161436
rs183068377	snp	G/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88758070	CTATGTTGCCCAGAC[G/T]GGTCTCAAACTTTTG	161436
rs183077306	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719428	GTATTTACAACTATT[A/G]ATAGTCTATCCCATA	161436
rs183088234	snp	C/T	0.000223722	0.0105741	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715186	AATATGTACAACTTC[C/T]GTCATATCTCTGTTA	161436
rs183146528	snp	C/T	0.0138799	0.0821421	intron-variant	EML5	GRCh38.p7	14:88625558	AAGCGCCAGCCACCA[C/T]GCCCGGCTAATTTTT	161436
rs183148060	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88650111	TTATTCACAAATACT[G/T]GAAATTTGACAAAAA	161436
rs183165337	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88668029	TTCGCCACAAGCTCA[A/C]TGAATGTTCTGGTGG	161436
rs183223947	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752606	ATCTCTTACTAATAT[A/G]AACAGGAGGCAGGGA	161436
rs183231664	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88730904	GCCTGTGCTTATTCA[C/T]TGTATTATTCTTTAG	161436
rs183260696	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691503	CATGTTCCTGTTACA[C/T]GAGGTCATATAATCA	161436
rs183265728	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88710227	AAGAGGGGTGGAATG[C/T]TTTGGGCTGAAATTA	161436
rs183333429	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742333	CTGCTAGTGTGACTG[A/G]GGAAATGAATTTTAA	161436
rs183371724	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643330	CTGAGGTACAGTTGG[C/T]CTTACATATCCAAGA	161436
rs183374486	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695086	TAATAGCCTATCATA[C/G]AGTAGAACACATTCT	161436
rs183381873	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713717	CACTTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	161436
rs183385350	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630431	TAACTCCTTACTGCA[C/T]ACTCAGCATCCATTA	161436
rs183415339	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88778757	GCACTCCAGCCTGGC[A/G]ACACAGCAAGACTCC	161436
rs183445079	snp	A/C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88773492	ATGAGTGGATTTGGC[A/C/T]AGGTCCTGAGGTTTT	161436
rs183448790	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88756245	TAACAGAAGAAAGGT[A/C]AAAAAAACTCCCATA	161436
rs183459301	snp	C/T	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88735003	GCTAGATACAGAACA[C/T]TGTGTGATAACAGTA	161436
rs183471234	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622047	CCCCTCCCCCTTGTC[C/T]GCCTCCAGTAACCAC	161436
rs183472822	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88653465	ATTACTTTGAGATAT[C/G]TTCCATCAAAACCTA	161436
rs183486726	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673848	CCTCTTCAAAAACTA[C/T]AAACCACTGCTCAAG	161436
rs183546145	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670972	TGAACAGAACAAAGT[C/T]GTAAAACGTACTTCA	161436
rs183552630	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614739	AAAAGAAATAAGGAT[C/G]TAAGAATTCAGCCCT	161436
rs183565175	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88658940	TTAACAAAAAGTAAC[A/T]ATCGATTGATTGCTT	161436
rs183577959	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698977	GTAAAGAGAGGTTAG[G/T]TAATTTGCCAGTAGC	161436
rs183608510	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88626184	AAATCATTTGAAAAT[A/C]ATGTTTCTTGATTTA	161436
rs183621602	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651366	CAAGCTAACATCAAA[G/T]ATTTCAGTTATGACA	161436
rs183630939	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88653885	ACCAGCTCCTCTTTG[A/T]ACTTCTGGTAGAATT	161436
rs183645493	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88769791	TTCAGATTCTAATCC[A/G]AAACCACAGGGCTCA	161436
rs183656864	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695840	ATATAAGAACTTTGA[A/G]TAATTATGAAAAGTT	161436
rs183677642	snp	A/G	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88735102	AAAAGACAAACTGGG[A/G]TAAACAAATCTCAAT	161436
rs183682506	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88741578	GGACACAGTGGCAAA[C/T]GCCTGTAGTCTCAGC	161436
rs183742305	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88724728	GAAAAAATGAAGCTG[A/C]TCATGAATATTAATT	161436
rs183747101	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631490	AAGTGCTAAGATTGC[C/T]GGGCACGGTGGCTCA	161436
rs183748715	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88655319	AGGCCTCAGGAATAA[C/T]GCCACATATCTACAA	161436
rs183776167	snp	G/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88636757	GCCATGGGAATGTGA[G/T]TAGATGTTCTAGATA	161436
rs183796444	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679354	TAAAGACAATGTAAC[A/C]TGGAAATGCTTTCTT	161436
rs183814914	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88718783	AGACTTTGGTTTGAG[G/T]CATGAAACTTAAGAT	161436
rs183822123	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88782241	GGCAGCATTTTGCCC[C/T]TGCCCTAGAGATCTG	161436
rs183826630	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88764510	TTCTTGGTCAGCCTA[C/G]CTAGAAGTTTATCAA	161436
rs183834896	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88745792	AAAGAAAATACATTG[C/T]TTTTACTGAAGCAAA	161436
rs183862375	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789119	ACTGGCAAAAGTTTC[A/C]AAATATAGACCAAGG	161436
rs183906888	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687115	TGATGCCCAACAAGA[C/T]GGAAAAATACATGCC	161436
rs183946270	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726791	TAGATATCTTAACTA[C/T]CTGTTGTGTGGCAAG	161436
rs183974936	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728365	CCATCAAAAAGCCAC[A/G]TCTAATGTTTAACTC	161436
rs184032666	snp	A/G	0.00277398	0.0371389	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687253	AGCTCTTTTTATAGC[A/G]TAGGTCTTGAGACAT	161436
rs184045221	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88786320	AATTTACACACATAT[A/G]TAAAATTTACCTTCT	161436
rs184046746	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766476	CCCCGGTCTCCCATA[A/G]CGCTCCCAGGCTTAT	161436
rs184051444	snp	C/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767022	CTTGTATAAATTGTT[C/G]AGATTTTAGTAATTT	161436
rs184054933	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748773	CAACACAGAAAACTG[C/T]TACATTATCTAAAAT	161436
rs184058481	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88664041	ACAGCACTTTGGGAT[A/G]CCAAGGTGGGAGGAC	161436
rs184082130	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88704785	GGGATACAGTCAGTT[C/T]TATCATTAGAGATGT	161436
rs184101681	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88747847	CAAAAGATGGACTTC[C/T]AGCCATGAAGGAGTA	161436
rs184121799	snp	C/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88629115	TACCAGATCACTCTA[C/T]ACATTTTGCCAGTGA	161436
rs184182199	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785131	TTTGTGGGATCTAAA[A/T]ATCAAAACAACTGAA	161436
rs184190196	snp	C/G	0.0352966	0.128072	intron-variant	EML5	GRCh38.p7	14:88617493	GTGCTACTTGGCTGG[C/G]TCCAGCAGCACATAC	161436
rs184199265	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640094	AGGCCCCCCAAAAAG[A/C]AAAACAAAAATCAAA	161436
rs184215315	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88661032	TATATTTATTGTTAA[G/T]AGTATATATTTAATT	161436
rs184218393	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88682194	TCTTTGGGAAACACA[A/G]TAAAATACCTCTGTA	161436
rs184243010	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711141	ATGGTGACTCTCATG[C/T]CCTGGCTATGTGGTG	161436
rs184292337	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723524	TAAGTTCTGAAGATA[C/T]ACTGTATGGCACAGT	161436
rs184305611	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732290	TCTACATATGGCTAG[C/T]CAGTTTTCCCAGCAC	161436
rs184312625	snp	A/G	0.00305949	0.0389921	intron-variant	EML5	GRCh38.p7	14:88754697	AGGAAATAAATAAGT[A/G]GTATTATTAAAAATT	161436
rs184313088	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701602	AAAAGGAAGAAGAAT[A/G]GGAGAAAGAAAAAAG	161436
rs184374464	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776296	CCAATCCTGGAGGAA[C/T]AGAGAGATGTGGCCT	161436
rs184376688	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692547	AGGATGTGCATAAAT[C/T]ATATGCAAATACTAT	161436
rs184386929	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790946	AGAAAAATGAAATGA[C/T]TTATCAGTTACCTTT	161436
rs184428773	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770554	GTGGGATCCAGTACA[C/G]AAGCAGCAGGATTAA	161436
rs184441280	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88687993	GGAGGATTTCTTGAG[C/T]CCAGGAGCTGGAGGC	161436
rs184442934	snp	C/T	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88732466	CTGTTTTGGTTACTA[C/T]AGCCTTGTAGTATAG	161436
rs184448063	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88706054	TTGATAGATTAAAAC[G/T]CAATCAAAATTACTT	161436
rs184503352	snp	A/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88622794	AACAAATACCAAGTT[A/T]TAAGCAGAATCTTTT	161436
rs184510055	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88748243	AACTCTATGAGGTCA[G/T]GCAAAGAAGAAATTC	161436
rs184515325	snp	A/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88727450	CCTGTTGTCCAGGCC[A/G]GAGTGCAATGGTGTG	161436
rs184516317	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88711751	GACTTTAAGACACAG[C/T]CTGGCCAACATGGTG	161436
rs184519145	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88643855	AGGTTGGGGAGGGAA[C/T]GACAGCAATCACCAT	161436
rs184523370	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664855	AAGCAAATGTCAAAA[A/G]CTATGTATGATGTAG	161436
rs184532239	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613097	TACTGTTGTGTTGCC[A/T]TTGCTTTTCCATTGG	161436
rs184581871	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88791537	ACTAAAGAAATGTCA[A/G]CAAGCTCTGGGACCA	161436
rs184582179	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770884	TATCATCTGAAATAT[A/G]TGGAAAGAACAGATT	161436
rs184592055	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755227	AATCCCTGCAATATA[C/T]TGTGTGTAAACTTCT	161436
rs184592116	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88651764	AAATACATATGTAGC[A/G]CTTATTGCTTTGTGA	161436
rs184594239	snp	A/C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671679	GTGTAAAGACACATA[A/C/G]AGGCTCAAAATAAAG	161436
rs184599916	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733950	TGATAAATTCAGCTA[C/T]ATGAAAAATAACAAC	161436
rs184601782	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693390	TACATGGTGACAGGC[A/G]AAATTGCTTATGCAG	161436
rs184605368	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777502	TGGGTTTTGAAGGTA[C/T]AAAACTCACTGGTAA	161436
rs184607789	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623250	CAAATACCTTGACCT[C/T]AGGTGATCTGCCTGC	161436
rs184616407	snp	C/T	0.000696483	0.0186482	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665482	AGAAAAACAGCAACA[C/T]CTCCCACCTGAAAGA	161436
rs184637773	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88706573	AAAAATTGAACAAAT[A/G]AATGAATCTGTATCA	161436
rs184739050	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88676940	GACAGAGTCTTGCTC[C/T]GTCTCCCAGACTGAC	161436
rs184741397	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88646254	GTGCTATATCTTAAA[C/T]ATCCAATAAGAAATG	161436
rs184745788	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697403	GAGAAGGTACTGGAG[A/G]TGGGCCTTCAGAAAG	161436
rs184751142	snp	A/T	0.0322114	0.122752	intron-variant	EML5	GRCh38.p7	14:88645045	TCTTTCTTTCTTTTT[A/T]AGACCAAGTTTCACT	161436
rs184767745	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688198	GTAGAAAGGCAGTGT[A/T]CCTTTACTTCTTAAA	161436
rs184784038	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88650656	TTTATTTATTCTCCC[A/C]GAGACAGGATCCCAC	161436
rs184808612	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775276	CCTTAGGTACCAGCA[A/T]GGCCATAGGGGTGGG	161436
rs184816362	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88758983	AGTAGATTAGTGATT[G/T]CCAGGTGCTGGAAGG	161436
rs184819642	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737106	AACTTCTTTCTTCTT[G/T]GATGTGGGACAAGAA	161436
rs184828724	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716268	AATGAGCCCCAAGAT[A/G]AATCCAAGATTGTAT	161436
rs184839577	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88665644	CCAGCCCGGGCAACA[C/T]AGCAAGACCCCATCT	161436
rs184889208	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763946	AGCATTTTAAAAATA[C/T]GAATAAGTATTAAAT	161436
rs184895940	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88625765	TCAACTGAAATTTGA[C/T]ATGGCACAAACATTT	161436
rs184906395	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669531	CCCTCACTGTGCGGG[G/T]CCTCCCTGCAGGAAT	161436
rs184926841	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710962	TCAATAAATCCTATT[C/T]ACTTGACTAAGAAAA	161436
rs184996902	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88781935	GTAAAGATACCCAAA[A/C]ATGTGGAAGTGACTT	161436
rs185011736	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745118	TAAGAACATGCCAGC[C/T]GTCTAATAAAATATA	161436
rs185089655	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677642	TGGGCAAAGGACATA[A/G]GCAGACAATTCTCAA	161436
rs185119940	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785904	CACTATTTTGATTAA[A/G]TAGTTCCAATAACTT	161436
rs185134464	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88716503	ATGGAGTAAGATTTT[A/T]AAGAAAAGTCTAAGG	161436
rs185165186	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88634271	TTCCACCATGATTGT[A/T]AATTTCCTGAGGCCT	161436
rs185194224	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88656952	AAATCCCTAAACCAA[C/T]AGTGTTAACACATAG	161436
rs185211107	snp	C/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88697806	AATGGCGCTATCTCG[C/G]CTCACCGCAACCTCC	161436
rs185219631	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759870	ACCATGTTACACTCT[C/T]ACCAGCAATGTAAGA	161436
rs185240974	snp	C/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88737775	CTCTTCTTCCTTCTC[C/T]CTTGTAGACAACTCT	161436
rs185245830	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628882	TTGTTCAAAGATTTA[C/T]GCAACTGTAAAATAT	161436
rs185247843	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653133	ATGCTTGTGATTTTT[A/G]CACATTTATCTTGTA	161436
rs185251401	snp	C/T	0.00136939	0.0261308	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702524	ACCCAGATAAAAACG[C/T]TGTGTGTTTTGCTGT	161436
rs185251771	snp	A/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766560	TCAAACCCGGTCTCC[A/T]GATGTTACCAATGAC	161436
rs185261603	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672929	GAGCCCAGGACCAGA[C/T]AGATTTACAGCTGAA	161436
rs185325083	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751735	TCCTGAAGAACACTG[A/G]TATTTAAGAAGCAGA	161436
rs185365384	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88694860	TTTAATAAATAGCAG[G/T]TTAAAATCTCTGACA	161436
rs185370814	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88744997	CTTTGAAATATTCAA[C/T]CACAATAATACTTTC	161436
rs185400022	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787635	ATCTCTTAATTTTAT[C/T]CCTTAAATTATGCAA	161436
rs185417139	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660142	TTTTACATTAGCCAG[G/T]CATGGTGGCATGTGC	161436
rs185418907	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768144	TAAAAATACCACAAA[A/T]ATTACATTTGTCCTT	161436
rs185422253	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88627207	GATTTACAATTATTT[A/G]TGTATTGAGTCCTTT	161436
rs185433881	snp	A/G/T	0.00159649	0.0282165	intron-variant	EML5	GRCh38.p7	14:88700957	TTTAAATAAGCTGGG[A/G/T]TTTTTTTTGCCCTAC	161436
rs185448356	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88781430	TTTGTTTTATCCCAC[C/T]TTGCACACACCACAG	161436
rs185501179	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722112	TAAAAAGTCAATAAA[C/T]AACAGATGCTGGTGA	161436
rs185511178	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88698430	CACCACCATGCCCGG[C/G]TAATTTTTGTATTTT	161436
rs185543663	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639280	GGCCTTCTAGACAGA[A/G]GAACACTTTAAGCAG	161436
rs185558267	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681618	TAGTCACAAAGGAGA[C/G]AAAAACTTAGCTTCT	161436
rs185560400	snp	C/T	0	0	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612440	GTTCTATACAGTGCT[C/T]TCATTTACTAATAAC	161436
rs185570770	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613795	TTACACAATCAGGAG[A/C]TTAGATACTGCACAC	161436
rs185584163	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88655903	AGAGAAATGCAAATC[A/G]AAACCACAATGAGAT	161436
rs185584446	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88635429	AAGCCTGGGTGAAAG[A/T]CTGGGAGTGTTTGGT	161436
rs185587148	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88763622	AACACTTCCAAACAA[C/T]AGAAAAAGAGGGAAT	161436
rs185588890	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88658010	AATATCAAAGTCATA[A/C]ATTCATGGCAACCTG	161436
rs185592632	snp	C/G	0.0107246	0.0724382	intron-variant	EML5	GRCh38.p7	14:88717056	ACATCACAAAGTAAA[C/G]GTACAGAGTTGATCA	161436
rs185599667	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678047	GAATCAACTCAAATG[C/T]CCATCGATATTAGAC	161436
rs185625418	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88620280	TTAAGCACTGAAAAA[C/T]AAAGGTTTAAGAAAC	161436
rs185641205	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88642789	GGAGTGTTTCTCCTA[C/T]ATTTCAATTACTATT	161436
rs185645799	snp	A/G	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88663467	TATATAGTTGAATAC[A/G]ATATAGTTGAATACA	161436
rs185649795	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88765300	TCTGGGGATGAGTCA[G/T]CTTCCAAGTTCATTC	161436
rs185653654	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767204	CCTTCTGGGGTCCCA[A/G]TGTTAGTTCAGTTTT	161436
rs185656429	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88794133	CATAGGAAATACCAA[C/G]ACAGAAATCTGACAA	161436
rs185656675	snp	A/C	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88747123	AAACAAACAAACAAA[A/C]AAAAAAGGGTCAGGT	161436
rs185658761	snp	A/G	3.31455e-05	0.00407083	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88685056	TTTTATCCACTTCTA[A/G]TATTTCACCATTCTT	161436
rs185658963	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88772917	CTCCCAAATCTTTGC[C/T]GCATTCATATTATTC	161436
rs185662992	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88725945	TGAGCGAAGGATCTT[A/C]CCGTTCACTGAGGTA	161436
rs185665064	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704200	GAGTGAGTTCTCTCT[G/T]GATTAGTTCATACAA	161436
rs185673448	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729063	AGTAATTCATCTTTG[A/G]ATTTTTCTATATATA	161436
rs185709992	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632542	CTCCAGTCACACTGA[C/T]CTTCCAGTTTCTTGA	161436
rs185715737	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689501	TTTTACTGGCCATCA[C/T]TACCTATTGATATCT	161436
rs185791419	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647213	TAAAAATACAAAAAA[C/T]ATTAGCCAGGCATGG	161436
rs185800621	snp	A/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88749426	AACCTGCACTACAAG[A/T]TATGATCATGAAAGT	161436
rs185803953	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666399	GCCTGGCTACTTTTG[A/T]ATTTTTAGTAGAGAT	161436
rs185806913	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88690390	TTTCAATCATCTGGG[A/C]AAATGGTAAATGTGG	161436
rs185811154	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88636862	AGCTTCCCAGGGAAA[C/G]GTTTACTTCATTAGG	161436
rs185816803	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707951	ATTCTAACAAATAAA[A/G]TTCCAAGTTCTAAGA	161436
rs185855069	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707575	AAGTTATAGAAGACT[G/T]GTATATCAGGATGTC	161436
rs185861965	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88640503	AAAATCTTCAAAGTA[A/G]ATTAAAACAGAGACA	161436
rs185884062	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786870	CAGGTATCTCTTTAT[C/T]AGCAGCATGAAAACG	161436
rs185884555	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683334	ATCCCTTTAAAGGAG[A/C]CTGAATTTGATTGGT	161436
rs185888960	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767747	TTATAAAAATGTTAC[A/G]AAATAGTACAGTTTT	161436
rs185899143	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88751544	TTTTTTGATAGTGTT[C/T]GAATAAAGAGAGAAT	161436
rs185908155	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88729293	TGATTTCAAAGGAAA[A/G]TCTTCAATACTTCAA	161436
rs185993194	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619140	GGAAGCGGAGGCGGG[C/T]AGATCACCTGAGGTC	161436
rs186008147	snp	C/T	7.05156e-05	0.00593741	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661828	CCAAGCAATTTTTTC[C/T]ACCTAAAAATGAAAA	161436
rs186015522	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713406	CAAAAAAAAAAAATA[C/G]TAATAGGTAATATTT	161436
rs186094460	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88773318	GTTTTCAGCTCATGA[C/T]GACACTGAACAGATC	161436
rs186116459	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88734825	CCAGAATGTGGGAAA[C/T]GCTGAATAAACTGTA	161436
rs186134530	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88619324	GAGCTGAGATTGCAC[C/T]ATTGCACTTCAGCAT	161436
rs186148559	snp	A/G	0.0154538	0.0865337	intron-variant	EML5	GRCh38.p7	14:88641162	CCAGATGGATTCAGA[A/G]CTGAATTCTCCCAGA	161436
rs186160742	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88666629	TGAAATGATATTTTT[A/C]TTATTAATGATAAAT	161436
rs186181694	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88708871	GGCCTAAACAGTGTA[C/T]CATCAATTAGTACAA	161436
rs186228970	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88739419	CTGGAGCCAATCCCC[C/T]CCAAAATATCAAGGC	161436
rs186251671	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88624841	ATAAAAGGTAATAAA[C/G]GAGAAGCATATGAGG	161436
rs186290949	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623489	GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT	161436
rs186298613	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648374	ATTATATTTTTTTGA[A/G]ACAGGGTCTTGCTCT	161436
rs186300099	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695266	AATAAAAAGTTACAT[A/G]TTTGCTTGATTTCAA	161436
rs186308073	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713902	GAATGCAGTGGCAAC[A/G]TAACGGCTCACTGCA	161436
rs186315643	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88735073	GAAATATTTACAGAT[A/G]AAATCAGGGAAAAAA	161436
rs186320078	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690699	GTCACTTATTTAAGA[C/T]GGCGAAATCACATCA	161436
rs186378063	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88761268	CAGGTTTGTTGCATA[G/T]GTATACATGTGTCAT	161436
rs186388751	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88773935	ACCAGCCTGGCCAAC[A/T]TGGTAAAACCCCACC	161436
rs186393960	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88756426	AAGCCTGAAAGCAAT[A/C]CCACTAAGTAAAGGG	161436
rs186477860	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734494	CTTAAGGGGCCACAA[A/T]ACAAAAAGAGATACA	161436
rs186496349	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88780801	AATGGTCTCGATCTC[C/T]TGACCTCGTGATCCA	161436
rs186505612	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652518	CTATCTCTCTGAGTT[C/T]CAAAATTCTTCAGCA	161436
rs186512496	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763469	GGAAGAAGTCGAATC[C/T]CTGAATAGACCAATA	161436
rs186518662	snp	A/G	0.000335109	0.01294	intron-variant	EML5	GRCh38.p7	14:88694422	TCTGAAATAAACATC[A/G]AAATGTTTTAGCTCT	161436
rs186521507	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88717555	CAAGATCAGAGAGAG[A/G]CCATCCTGGCTAACA	161436
rs186577927	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777782	GGAGCTCAAGACCAG[A/C]CTGGGCAACATGGCA	161436
rs186587537	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698792	ATTTTCAATTGTCTA[C/T]TGGACATCTCACCTG	161436
rs186590548	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88762277	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	161436
rs186597145	snp	A/C	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88741509	TAGGTGGAATTAGGT[A/C]AATTTTTATAGTTCA	161436
rs186607408	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628278	ACAAAGGCAGTAGAT[A/G]GGAAACCACCTGAAT	161436
rs186659351	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747438	ATAATAAGCTGAAAA[A/G]ATAAACAAACCACCC	161436
rs186663231	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755719	GAATCAAGGCTGGGT[A/G]TAGCGGCTCATGCCT	161436
rs186666841	snp	A/T	0.0312799	0.121085	intron-variant	EML5	GRCh38.p7	14:88726510	ATCACTGAAGATAAA[A/T]TTATTATGTGTTTCT	161436
rs186711518	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88631779	CCATCTCAAAAAAAG[A/G]AAAAAACAAAACAGA	161436
rs186714851	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88655323	CTCAGGAATAATGCC[A/G]CATATCTACAACAAT	161436
rs186726460	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88676487	ATTACCTCCCACCAG[G/T]TCCCTCCCACAACAT	161436
rs186728547	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783411	AGATCAATGGAGCTT[C/T]CACTGATCCAAGAAA	161436
rs186728718	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88672576	AGGAGATAGAGACAC[A/G]AAAAGCGCGTCAAAA	161436
rs186732254	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88736649	CCCTATGCAGATAGG[C/G]GCAAGTCCCGGTGAA	161436
rs186733673	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697259	GTATGCTAGATACAA[C/T]GAGCAATAAGACATT	161436
rs186735304	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88784582	ACCTACCAAGATTGA[A/C]CCAGGAAGAAATCCA	161436
rs186735469	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765891	GGAAGTCAGGGACCC[C/T]GAACGGAGGGACCGG	161436
rs186741864	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715714	TTAGGCTGGAGTCCA[C/G]TGGCATGATCTCGGC	161436
rs186744258	snp	C/T	4.99646e-05	0.00499798	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712372	ACTGAATTTATATCG[C/T]TGATATCTGAATACT	161436
rs186763002	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88762478	TCATGCCATTGCACT[A/C]CAGCCTAAGCAACAA	161436
rs186770126	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787141	TACCTTCTTTCATTT[A/C]TTCTGATGACCCTTC	161436
rs186782827	snp	C/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88719121	CTAGGCATGGTGGCT[C/G]GTGCCTGTAATCCCA	161436
rs186806861	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679466	GGAGGCCAAGGTGGG[C/T]GGATCACTTGAGGTC	161436
rs186830835	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616068	TTTCATAAACCAAAG[C/T]TGTAGGAGTTGTTGT	161436
rs186838376	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88637641	TCGCACATGGCAGGT[A/G]TTCAGTAAATTTGTT	161436
rs186852850	snp	C/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88659480	GCCTCCCAAAGTGCT[C/G]GGATTATAGGCGTAA	161436
rs186859869	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88680770	CAAAAAAAAGTCCTC[A/G]ATCCAGACATCATGG	161436
rs186867589	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88699955	TGAATTATATCTATA[C/T]ATACACACACACATA	161436
rs186883379	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88624127	GTCACCCAGGCTGGA[A/G]TGCAGTGGCACCATC	161436
rs186911241	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88659080	AAAGTTTAAGTTATT[A/G]TTATTATGGTATTAG	161436
rs186951591	snp	A/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88742722	ACAGTGCTTATATCA[A/T]GTGCCTTAAAGCCCA	161436
rs186959986	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88719900	TGCTAGCTAGACTAA[C/T]GAAGGAGAAAAGAGG	161436
rs186973469	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778211	ACTAAAATAAGACCT[C/G]AACGAAAGAAGGAAA	161436
rs186985087	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88741954	TTGTAATTTTTAAAC[C/T]TAAAATCTCCATAAT	161436
rs186995093	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88703765	GAGAATCCAGAACCC[A/G]TATTTTGGTGAAATT	161436
rs187032500	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88699251	GTAAAAGATGTGAAA[C/T]AGCATTATACGTGTT	161436
rs187049259	snp	A/G	0.000381923	0.0138136	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746259	AAACTGCATTCTTTG[A/G]ATCAAGTCCAACTGA	161436
rs187075081	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88770464	ACATCATTTGTTGAC[A/G]AGAGACCATTCAGTA	161436
rs187141240	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88782859	CTGAGGTGGGTGGAT[A/C]ACCTGAGGTCAGGAG	161436
rs187175280	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790330	TAAAATCATAAGCAT[A/G]TATATTCAACGATGA	161436
rs187196661	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88684096	TATCAGAACTAATAA[A/G]TGAGGACGGCAAGTT	161436
rs187219294	snp	A/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614542	AAAGCGATCTATTAT[A/G]CTATAAAGATAATTA	161436
rs187240982	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88765002	TGCTGTTTTCTATGC[C/T]ATGAATAATAAAGTC	161436
rs187253813	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725661	TAAGAAGAAAGCACA[C/T]AATGTGTTTTAAAAG	161436
rs187287118	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664860	AATGTCAAAAGCTAT[C/G]TATGATGTAGTTTTG	161436
rs187290763	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88688001	TCTTGAGCCCAGGAG[C/T]TGGAGGCTGCAGTGA	161436
rs187302352	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706186	AGATTATACTTTAAT[A/G]TAAAATTGTTATTTG	161436
rs187312020	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615071	ATTGTTCATCATACT[A/G]CTTTTCCATTAGTGA	161436
rs187315255	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727627	GGTCTCAAACTCCCA[A/T]CCTCTGGTGATCCAC	161436
rs187376993	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786198	AGGTCTTCCTGGCCA[C/T]CCTATCTAAATACCT	161436
rs187380667	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766921	GGGCTGGTTTCCCCC[A/G]ATAGCACACAGTTAT	161436
rs187385811	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658549	GCAGAATAAAAGATA[C/G]CAATTCCTAAACCTG	161436
rs187388808	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769172	CCCCAACCAAATCTC[A/C]TGTTGAAATGTAATC	161436
rs187389533	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88748370	ATACCTCTTTGAACT[C/T]GCTGGGCAGTCATTA	161436
rs187517595	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731030	CACTTTCAGTTCTGT[A/G]AATTTATTTTTTGTA	161436
rs187582930	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668688	CACAGTTCCCTGTTT[G/T]ACTCAATGCTTATTC	161436
rs187584395	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691532	CAGCTCACATTATTA[C/T]TGCATCAAAAACTTT	161436
rs187587569	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88789342	TCTGACATTGAAACT[A/G]ATTGCCATATAAACC	161436
rs187587703	snp	C/T	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88769830	TTCTCCCTTTATTTA[C/T]AACTTCTTACTCCAA	161436
rs187593666	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88710738	GAAAATAAATTACTA[A/G]CAAAAAAGCTAACAA	161436
rs187598540	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88753502	AGATAACTAAAATTG[G/T]TCTAAAATTTAAAAT	161436
rs187630289	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788223	ATGTTATTCTGAATC[A/G]CTTTTCCAATTACAA	161436
rs187641025	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636102	TTAGAACTCCATCCA[C/T]CCCTACACAAAGAAC	161436
rs187642452	snp	C/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88643138	GGAGTATGCATTTTT[C/G]ATGTTTTACAAACTT	161436
rs187654024	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88752339	AACACCTTAAATAAG[C/T]GGTTTTTAAAAATAA	161436
rs187657003	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88678419	AACCTGCACATCCTG[C/T]ACATGTATCCCGGAA	161436
rs187666783	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88758646	CTAAACAAAGTTACC[A/G]TATGATCCAGCAATT	161436
rs187703925	snp	C/T	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88622062	CGCCTCCAGTAACCA[C/T]TATTCTACTCTCCAC	161436
rs187713555	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88643585	CCAGGGGGAATCTAT[C/G]CCCCATGGACATAGA	161436
rs187728818	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664424	TTGAATCACTTTTCC[A/G]TTTCTCTAATATAGC	161436
rs187815283	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88621707	GCTGAAGATAATATC[C/T]GTATGATTTATAAAT	161436
rs187818127	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88626111	ACTTCCAGCTGTATG[A/G]TAAGCAGTGTGTTAA	161436
rs187895473	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88754374	GTTATATATCAACCT[C/G]CCACCCCACCTACCC	161436
rs187905568	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88779046	CTCTTTTCTTCTGGC[A/G]CAAGCAACCATCAAT	161436
rs187911753	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88743521	GAATATACACTGCCG[C/T]CTTATTTAATCATCA	161436
rs187921402	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88721395	CAGTAACCAAAACAG[A/C]ATGATGCTGGTATAA	161436
rs187927215	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88663590	AATACAAACATACTC[A/T]TTAAGTTCTTTATGT	161436
rs187934921	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88669672	CCCTCTACCAGCTCT[A/G]AGGAATCTGGGCAGT	161436
rs187935558	snp	A/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88774445	AGTTTTGTGTACCAA[A/T]AATGACATGACTCAT	161436
rs187944763	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88704605	TTACTCTAAGTCAAA[G/T]ATGCCCAGTTGTCCC	161436
rs187948138	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88711085	ACTACTGAATCTCAC[A/T]CTTCATAACCAGGCA	161436
rs187994910	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690998	ACTTCTCTGCACCCA[A/G]GGTCTGCCTCCCTGG	161436
rs188060750	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625389	AATTCTAACATACTA[C/T]AATTCTAGGGTTTAT	161436
rs188075108	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88649419	GTTTCAGAAACTCTT[C/T]CAAGACATTTTCACA	161436
rs188078599	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667386	ATAAGACCGTGACTA[A/T]ATTTGAGAATAGCGT	161436
rs188090191	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88696321	CACCCTAGCTTTCAC[C/T]GTAGATCTATCTGTA	161436
rs188095220	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782253	CCCCTGCCCTAGAGA[C/T]CTGTGGAACTTTGAA	161436
rs188095397	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88764552	TCAAAGAACCAACTT[C/T]AGGTTTTTCTCTATT	161436
rs188104159	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88650915	CCAAAGCACTGAGAT[C/T]GCAGGCATGAGGCAC	161436
rs188105617	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745993	TCAAATCATGTTTCC[A/G]AGTCCTACAATACAT	161436
rs188134830	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774272	ATGCCGTTGCTAGTC[C/T]GAAGACCACACTTTT	161436
rs188144778	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88735137	AAATTTGATCAGTGG[C/T]TCTCAAACTTTTGAG	161436
rs188172679	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654073	TTTATTTGCGTAGAG[C/G]TCTTTATAGCATTCT	161436
rs188186206	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732297	ATGGCTAGCCAGTTT[C/T]CCCAGCACCATTTAT	161436
rs188190248	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763389	CAACTTTATGCAAAT[A/G]AACTAGAAAATCTAG	161436
rs188224995	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691823	CAAAAGTAAGGAAGG[C/T]TGAAATGCTCACCAA	161436
rs188288634	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635452	TGTTTGGTCTGGAGA[C/G]ACTAGGTTTGTCTCT	161436
rs188308781	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88678052	AACTCAAATGCCCAT[C/T]GATATTAGACTGGAT	161436
rs188317111	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88698578	CTTCCTTGACTCCTA[C/T]TACTGAGTTTCCTTC	161436
rs188337344	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88739480	TTATATGGATAGAAC[A/G]TAAAAGAAAATAAAT	161436
rs188343685	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717320	GAATGGACACAAACA[A/G]GGGGACTTTGGTGTG	161436
rs188345359	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767070	GTTATATCCTGAGCA[C/T]TTCGAATATTAAGTT	161436
rs188368510	snp	A/T	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88675727	CTGTCACAGTCAGGC[A/T]GCAAATTTCCTGAAC	161436
rs188384425	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88714575	CACACAAAAATGGTA[A/T]CTGTGAAGTGGCAGA	161436
rs188423119	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88761584	GCCACATTTTCTTTA[C/T]CCAGTCTATCATTGA	161436
rs188423830	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757924	GACACAATCACCACT[A/C]ACTGCAGCCTCGACC	161436
rs188425262	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88786561	GATAAGGTTTGGCTC[C/T]GTGTCCCCACCCAAA	161436
rs188446983	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763726	AATTTCAGGCCAGTA[A/T]CCCTGATGAACATCG	161436
rs188447604	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88630856	ACCAGCCTTATCGGT[A/G]AAGCCAACACTGTGG	161436
rs188508604	snp	G/T	0.00438332	0.0466095	upstream-variant-2KB	EML5	GRCh38.p7	14:88794338	AGCAGTTTACATGCA[G/T]GAAATAAAGGCCATC	161436
rs188577206	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88629449	ACACTTAGACTGTTC[C/T]AAACTTACATCAGTA	161436
rs188586182	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723565	AATAATAATGTAGAA[C/T]ATACTTGAAAATTGC	161436
rs188640416	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88640418	AAAACCACACAATTA[A/C/T]GTAAAAATTAAATAA	161436
rs188642405	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88661077	TATTGAAGTTAATAT[C/T]GGGGATAAAAGGAAT	161436
rs188655000	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88682204	ACACAATAAAATACC[C/T]CTGTAACAACTTTAG	161436
rs188659382	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88701651	TTCAGGAAAGCTATA[C/T]AGGAGGATGCAAGTT	161436
rs188669990	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764075	AACCAGCCTTGTATT[C/T]CTGGAATGAATCCTA	161436
rs188674642	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745132	CTGTCTAATAAAATA[C/T]ATCCAACATTTTAAT	161436
rs188685479	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88785230	TGGGGATGGTTAATG[A/G]GTACAAAAAAAGAGT	161436
rs188703828	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88747887	GAACTTACCCTCCCC[A/G]ACCCACCCCTGCCAT	161436
rs188710659	snp	C/T	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88625707	GTGCCCGGCCTGAGC[C/T]ACGGTGCCTGGCCTG	161436
rs188714581	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88781648	CTGAATCATGGTGAC[A/G]ATTACTCTCATGCTG	161436
rs188732306	snp	G/T	0.000116454	0.00762978	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704885	AGTGTAATCGAATAC[G/T]ATTTCCTGGAGCCCG	161436
rs188738229	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88745046	GTCATATTTTGTAAC[A/G]GGTCTATTTATATAA	161436
rs188783266	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88643895	TTACGCCTTGTTTAC[A/G]TTTGATTTAGCAGAG	161436
rs188797120	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613243	TAAGGCTGTTGTCTT[C/T]GGCTTGGGTGAAATG	161436
rs188805733	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88634643	GGCACTCATTTCAAT[C/T]ATACATACTTATTAA	161436
rs188832949	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88787163	TGACCCTTCTCCCTA[C/T]TGTCCTCAAAGACTT	161436
rs188837004	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767950	CCAGGATCCCATGCT[A/G]CATTTTAACTGTTAT	161436
rs188874520	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88653472	TGAGATATGTTCCAT[C/T]AAAACCTAGTTTATT	161436
rs188885505	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660046	TTTAGGATGCCGAGG[A/C]AGGAGGATCACCTGG	161436
rs188898689	snp	C/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88700449	AGTAGATGGACAAAC[C/G]AGGAGCATCCCTGAG	161436
rs188905912	snp	G/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88687401	CTTTTTCCTTATATT[G/T]AAAACTTCTAGAAAA	161436
rs188955346	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730370	CAATGAGGTTGCAAG[A/G]GAAGTAAGTTTCTGA	161436
rs188958434	snp	C/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88693432	TTTATAAAACCATCA[C/G]ATCTCATGAGACGTA	161436
rs188966310	snp	C/T	0.030665	0.119967	intron-variant	EML5	GRCh38.p7	14:88711942	AGTGAGACCCTGTCT[C/T]AAAAAAAAAAAAAAA	161436
rs188968681	snp	C/G	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88617178	TGAGACGGAGTTTTC[C/G]CTCTTGTTACCCAGG	161436
rs188969854	snp	A/G	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766478	CCGGTCTCCCATAGC[A/G]CTCCCAGGCTTATTG	161436
rs188989719	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88727091	TTAGCACAGTTATAG[C/T]GTCACTGCATAATAA	161436
rs188992286	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88755513	TCTCTAAAAACAAGA[C/T]AAAGACCTAGCAGTT	161436
rs189000528	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88733977	CAACAACAACAACAA[C/G]AATTTTTGCTTACCT	161436
rs189004031	snp	A/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88770570	AAGCAGCAGGATTAA[A/T]ATTGGATAGGAGCTG	161436
rs189017188	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732593	TTTTTTCCACTTCTG[C/T]GAAGAAAGTCATTGG	161436
rs189036342	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703279	ATTTGTATTTGTTGT[A/G]TAAGTATTTCTGAAA	161436
rs189066667	snp	A/G	0.00100326	0.0223746	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792302	CGGCCCCCGCTCCCC[A/G]GTACCTGATGATGTC	161436
rs189083547	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771635	TATTGTGTTAACATA[C/T]TTCAAAGTAGGCATT	161436
rs189134034	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88617390	GACCTCAGGTGATCA[C/T]CCCCGCTCGGCCTCC	161436
rs189150257	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88639494	AGAGTCACACAGAAA[C/T]CAGTAGTAATTTTCC	161436
rs189154283	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88660641	CCAGCTACTCAGGGG[A/G]CTGAGGCAGGAGAAT	161436
rs189165647	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88709819	TATACTTACAACACA[A/G]TATTTTGCAGCAGTG	161436
rs189170187	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88681333	AACTTGGAATTGGCC[A/G]GGGGCCGTGGCTCAC	161436
rs189182097	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88689138	CTATTAATGGAGATT[A/T]AAGTTACTTCCAAGT	161436
rs189229785	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759044	CTTGGGAATTTTTTA[A/G]GGGTGATAAATATTC	161436
rs189236909	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88737460	AGCGCAGCCTGCCAG[A/G]CCAAGTGGGCAGGGT	161436
rs189246936	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716433	AACATTAAATCCATA[G/T]ACCGTATTGCCCTTT	161436
rs189247780	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728568	ATTCATTAAGTAGAA[C/G]TGGATCATCATAAAA	161436
rs189254573	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638285	GGTAAAAGAATACAG[A/G]TATATTTCAAAACAG	161436
rs189263376	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645444	TTTCTTGATAGGTAC[A/C]TTAACAACAAAGCCT	161436
rs189273053	snp	A/C	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88791033	AACAAACAAAAAAAA[A/C]CAACTGAATACAGAG	161436
rs189283087	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88623567	CTGGGATTACAGGCA[A/C]CATGCCTGGCTAATT	161436
rs189285925	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88725378	AAAGGGGAGTCAGCA[C/G]GTGTAGAGGCTCAGA	161436
rs189290006	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88754894	CTGCAACCTCCATCC[C/T]GCCAAGTTCAAGCAA	161436
rs189297165	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88697536	ATCTACTGCAGCACT[C/T]TGTCACTTATTTTTT	161436
rs189299037	snp	A/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646410	TTTGGATGCCCACAA[A/G/T]TAAAAATAAAACTGA	161436
rs189299316	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88665836	CTGTTTGAGCCCAGG[A/T]GGTTGAGGGTGCAGT	161436
rs189309851	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88689552	GGACTCACAAATTCC[G/T]TCCTTCCTTCCTTCC	161436
rs189310391	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683648	AACCAAGTGGGATTT[A/G]TCCCAGGAATGCAAG	161436
rs189313473	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88775937	AGACTCCATTTGTTT[G/T]GGAGAAAGTAAGAGA	161436
rs189319573	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707707	AAGTTATAATTTACT[C/G/T]CTGCTTAATAGTAAT	161436
rs189439638	snp	G/T	0.0111196	0.0737302	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626457	AAACCCTGTCTCTAC[G/T]AAAAATGAAAGAAAA	161436
rs189441742	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88651478	TTTAAGTGTTTTACC[A/G]TGAATGAAGCAGACT	161436
rs189449918	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671351	TTTTAGACAAGCAAA[C/T]GCTGAGGGAATTGGT	161436
rs189460027	snp	C/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88692861	TGTAATTTACAACTT[C/G]AAAGTTACTTGAACT	161436
rs189469568	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711266	GTAATCCTCATGTGT[C/T]GAAGGAGAGACCTGG	161436
rs189472219	snp	A/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88707019	AAAATCCAGATATTT[A/T]AAAAAAATCTTTCAA	161436
rs189479305	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88712559	ACTGTACTGAGAACA[C/T]AGTAAATTCCAAAAT	161436
rs189523810	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748954	ATCAAGTGGTCTAAC[A/C]TACAGGTAATCATGG	161436
rs189543000	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623294	AGTGCTGGGATTCCA[A/G]GTATGAGCCACTGTG	161436
rs189544139	snp	A/T	0.0387552	0.1337	intron-variant	EML5	GRCh38.p7	14:88755840	TCTACAAAAAAAAAA[A/T]TTTTTTTAATGAGCC	161436
rs189548237	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782053	GACTTGGAGGGCTCC[A/G]AAGACAGGAAGATGT	161436
rs189551626	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88665547	AATTTAAAGTATGGG[A/C]CAGGTGTGGTGGCTC	161436
rs189574135	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88784725	GACAGGCAGTAACAA[A/T]TGCTGGAAAGGATGT	161436
rs189591477	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766201	AACAATATGAAATCT[A/G]GGCACCTTGAAAAAA	161436
rs189592553	snp	A/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88777703	GAGGATGGGCCGGGC[A/T]CAGTGGCTCATGCCT	161436
rs189655237	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734839	ACGCTGAATAAACTG[A/T]AAGAAGAACAAAAAG	161436
rs189697719	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88623047	TTAAGATGTAGTCTC[A/G]CTCTGTCTCCCAGGC	161436
rs189705173	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629018	TATTATTCATTCATT[A/C]AAAGTCAAAGTACCC	161436
rs189709541	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88653270	ACTTCCTCTTTTCCT[A/G]TTTGAATACCATTTA	161436
rs189721543	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673716	TGCAAAAATTACAAG[C/T]ATTCCTATATACCAA	161436
rs189728328	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88657286	GAATATCACTGTTAC[C/T]TAGTTTGTGTAAAAA	161436
rs189729210	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88695063	GAACATGGTCTCCAA[C/T]AGCTATATAATAGCC	161436
rs189737146	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713698	TGGGCTCAAGAGATC[C/T]TTCCACTTTGGCCTC	161436
rs189806729	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776429	GACTGAAATAATTTA[C/T]AAGAACCAAACAGAA	161436
rs189809988	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772957	GGCAAATATAACTTG[C/T]TCAGAGAAGCTCTCC	161436
rs189817305	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88763429	ATAAATTTCTAGACA[C/T]ACACACCCCCCCAAG	161436
rs189821037	snp	A/C	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88737811	TGTCTACTTGCTCAG[A/C]CAGTCTTATAACACT	161436
rs189821374	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88743118	CAAAGTAAATAGTGG[C/T]TATCAAGGCTGAGAG	161436
rs189821510	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88787955	AACAGAATAATCTGA[A/G]GCACTTTTTAAAAAA	161436
rs189829419	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734555	CAGGGTGTGATCAAG[A/G]AAAAAAATGTAAGAA	161436
rs189843289	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88697945	TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCAAAC	161436
rs189909522	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88779580	AATTAAAAAGCTCAA[A/G]TTGTCCCATGTAGAA	161436
rs189937819	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613801	AATCAGGAGCTTAGA[C/T]ACTGCACACAAAAAT	161436
rs189985655	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677841	GAACACTTTTACTCT[A/G]TTGGTGTGAATGTAA	161436
rs189993103	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652274	CTGAGGTACATGAGG[C/T]ATACCATCAGCAAAC	161436
rs190011924	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663496	CATGAAACAATAACA[A/T]CCTTAAAAAGAGAGG	161436
rs190022144	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88685360	AGTCTATGATTCTAT[C/T]CTCACATTCCCTCCT	161436
rs190032696	snp	C/G	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88704298	TGCTAGGTAACACAC[C/G]TGCTCCCCCTTTGCC	161436
rs190058663	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765471	AACGGCACATTGAGT[C/T]CTTCTCAAGCTTTGA	161436
rs190063221	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88747230	CAGCCTGGGCAACAC[A/G]TTGAAACCCCGTCTC	161436
rs190067743	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88760498	TTCCACAAATTGCAC[C/G]CTGTATTTTACACCA	161436
rs190073367	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725948	GCGAAGGATCTTACC[A/G]TTCACTGAGGTAGAG	161436
rs190074381	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88722722	AGCTTGTGGGAATTA[C/T]TTATATCTTACTGCT	161436
rs190082045	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88716689	TAAGAAGAGAAGAAC[A/G]TCTTATGTCCAAGGT	161436
rs190082483	snp	A/G	8.93408e-05	0.00668299	intron-variant	EML5	GRCh38.p7	14:88681865	GTGAGAGCTTAATCT[A/G]CGTTCAAGTGTGAGA	161436
rs190142973	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88783584	AAGTCACCGTATAAT[C/G]ACAAAGGGGTCAATT	161436
rs190217273	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628681	TAGAGAAACATTAAG[A/G]CAAGCTGCCTTAAAT	161436
rs190234344	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88633023	TTTTCTGTTCAATGT[A/G]ATAAACTAAAGCCTT	161436
rs190242951	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88701068	TCATCTCTATGAGGG[A/T]TTCTTCGATTCTACT	161436
rs190312249	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88751581	TTAAATGTAGAAAAT[A/G]GAATATCTACAGAAC	161436
rs190317469	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88729393	GGCCAAACCAGGCCT[A/G]CTGCCTATTTTTGTA	161436
rs190325342	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627234	CTTTTCACTTATCTT[C/T]GCTCCATTAACTTTT	161436
rs190351122	snp	C/T	0	0	intron-variant	EML5	GRCh38.p7	14:88677271	AAAATTGAAGCTGGA[C/T]CCCTTCCTTACACCT	161436
rs190351884	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615194	ATACTGCTAACTTTG[A/G]ATCTGTTCCTGAATT	161436
rs190359530	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786885	CAGCAGCATGAAAAC[A/G]GACTAATGAACCAAC	161436
rs190363800	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666475	AGGTGAACCACCTGC[C/T]TCAGACTCTCAAAGT	161436
rs190368712	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637290	ATTTACCTCTGTACT[C/T]CCCAGATTTTGACTT	161436
rs190369299	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88749766	ACAGAGTATGTTCTC[C/T]GACAAAAACAGAATT	161436
rs190370578	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690501	AGAAGGCAGAGTCAT[C/T]AGTGACCTTGTAAGA	161436
rs190372328	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659201	TTATACAAAACACAG[G/T]GATAGCAAAATTTGT	161436
rs190378120	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88708121	GATAAACCAAGGCAG[C/T]TAAACAAGAAAGTTG	161436
rs190384457	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88679566	CCGTGGTGGCGCACG[C/T]CTGTAGTCCCTGTTA	161436
rs190464296	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612832	AGGCAAGAAGTGTCA[A/T]ATGCTTTAGAGTTAA	161436
rs190503790	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88619340	ATTGCACTTCAGCAT[A/G]GGCAACAAGAGCAAA	161436
rs190514075	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642588	TGGGAAAATAGAATT[A/G]AAGTTACAAACGGTT	161436
rs190520681	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619155	CAGATCACCTGAGGT[C/T]GAGAGTTTGAGACCA	161436
rs190530375	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88662958	CGTGTAACTAAACGA[C/T]AGAAAGTAGGTATCA	161436
rs190535640	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662143	AAGATTCTTACAGTT[A/C]ATGTTTAAATTTCTA	161436
rs190537126	snp	A/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88684460	CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGTTTT	161436
rs190586423	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656038	TGTAAATTAGTTCAA[C/T]CATTGTGGAAGACAG	161436
rs190589693	snp	A/T	0.0119091	0.0762411	intron-variant	EML5	GRCh38.p7	14:88704662	AAATCCAGATATTTT[A/T]AAAAATATCTTTCAA	161436
rs190618831	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767505	TCCCACAACTGGGCC[G/T]GCCTCTGGACAAAAA	161436
rs190630974	snp	A/G	0.0166325	0.0896639	intron-variant	EML5	GRCh38.p7	14:88729084	TCTATATATATAAAC[A/G]CATCATATATATATA	161436
rs190664121	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88747604	AATAAGCTTAATGTG[C/T]GAAATAAAATTAAGG	161436
rs190665826	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773362	CAAAAACTTTGCTTG[G/T]TAATAAATCTCCAAA	161436
rs190737018	snp	A/C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88774100	TCCAGCCTGGGTGAC[A/C/G]AGAGCGAGACTCTGT	161436
rs190748450	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88756529	AAAAGGAACAAAAAG[C/T]AAAAGTAAAGATCTC	161436
rs190777876	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640718	AAAATCAGAGCAGAA[A/C]TGAACAATACTGAAA	161436
rs190791250	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673057	CCAGCATGATCTTGA[C/T]ACCAAAACCTGGCAG	161436
rs190802677	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88713971	ACCTCCCGAATAGCT[A/G]GGACCACAGGTGCAT	161436
rs190808095	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88648873	CATACTCTGAACTCA[C/T]ATCTTTGTACACACC	161436
rs190828610	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88690700	TCACTTATTTAAGAT[A/G]GCGAAATCACATCAC	161436
rs190894732	snp	A/C			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768501	CTGCAACTTCCACTT[A/C]CAGGGTTCAAGTGAT	161436
rs190914249	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729797	AACTCTTGGCCTCAT[A/G]TGATCCACCTGCCTC	161436
rs190923510	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726727	AGCTAATGCATACTT[C/T]AGTAAAAATATTTTG	161436
rs190930061	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88756222	TGAAATCAACAAATA[C/T]GGCATATTAACAGAA	161436
rs190930316	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88686765	TCAGTGAGTTATGAT[C/T]GCACCACTGCACTCC	161436
rs190942545	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625476	GTGCGATCTCAGCTC[A/G]CCACAACCTCTGCTT	161436
rs190946939	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88649585	AGGTTTAAAATTGAA[C/T]AGTCTTTCACTTAAA	161436
rs190949963	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667903	TAGGTTAAGCTCTTC[A/C]AGCAGTGGTTCTGAC	161436
rs190971436	snp	C/G/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88710057	TAACGTAACTCTGCC[C/G/T]TCACCTCTCCATTCT	161436
rs190983783	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778008	TTAAAAATGAGGGGA[A/C]CAAGTTAGGGCATAG	161436
rs190990392	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730399	GAGTGGTTGATTTGT[C/T]AGCCAAGCAAGGAAA	161436
rs190995680	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88762308	CTGAGGTCGGGAGTT[A/C]GAGACTAGCCTGACC	161436
rs191006841	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88741511	GGTGGAATTAGGTAA[A/G]TTTTTATAGTTCACG	161436
rs191051852	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88625245	CAAAGAGCATGCATC[A/G]TGTAGTGGCAGCAGC	161436
rs191070188	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667051	TGTGGGGTGAAAGGC[A/G]TCAAGGGCATGGTTT	161436
rs191090563	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88655523	TAAAACCATAAAAAC[C/T]CTAAAAGAAAACCTA	161436
rs191098624	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676897	GGAGAGGATTTCCTA[C/T]TTATTTGTTTGTTTG	161436
rs191103099	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88697271	CAACGAGCAATAAGA[C/T]ATTCAGGTAACTTTT	161436
rs191138361	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88758744	CACAGCAGCATCATT[C/T]ACAAATGGCCAAAAA	161436
rs191146625	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736686	CCTTCAAACCTAAGA[C/T]AGTTTAAAGCCTGAA	161436
rs191151989	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751769	GGAAAGACTCCTTTA[A/G]AGATAAAAATAATCA	161436
rs191154966	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715975	AAAGATGGATAAATA[C/T]GTAGTAAAACACCAC	161436
rs191170132	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88672678	AGAGAAGAATCAAAT[C/T]GACACAATAAAAAAT	161436
rs191170675	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88631802	AAAACAGAAAAACCC[A/C]AAGTGCTATGATTAC	161436
rs191176674	snp	G/T	1.66421e-05	0.00288458	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88643020	GAGCTCCAACACAAG[G/T]TCCTATAATGATAAT	161436
rs191181785	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709186	AAATATCTTTCTGAC[C/T]CTAGTAAAAGTAAGA	161436
rs191323808	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88624499	AATTTTGAGGTCTTG[C/T]ATAAAACAGTTTAAA	161436
rs191329006	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88637786	TTCCTTGTGCACAGT[A/G]AAAATAAGACTTCAC	161436
rs191347805	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88786787	CTTTCACTTCCCACC[A/G]TGATTCTGAGGCCTC	161436
rs191399491	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88720160	AATAGCCTACCAACC[A/G]AAAAAGGCTCATGAC	161436
rs191407106	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88652720	TGGATCTTTTCCTTT[C/T]TTGTTCTTTAAACCT	161436
rs191416975	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88620616	TATACAAACAGCCAT[A/T]TTTTAGCATACAATT	161436
rs191419311	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88694723	TTTAAAACAATACTT[C/T]GTTATAGCTTAAGAT	161436
rs191430143	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88659808	TGAGTTTTCAATGAG[A/G]ATTTTTAAACCTGTG	161436
rs191438077	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88626183	TAAATCATTTGAAAA[A/C/T]CATGTTTCTTGATTT	161436
rs191440046	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88680833	ATTCCCACAGGTAAA[C/G]TCCAATCAAACATGA	161436
rs191450550	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88700038	TACATTGTGAGCTCC[C/T]GATAGTGGCAGCCAG	161436
rs191452480	snp	A/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88651023	TTTAAATAAACCATG[A/T]ACCATATTATCTCCT	161436
rs191453723	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88778387	CAATTTTGAGTGTAC[A/G]ACTTTTCTCAGAAGC	161436
rs191473039	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88699319	TTTACAAAGAGGCAA[A/G]TAGAAAGAGATAAAA	161436
rs191474817	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88741978	CCATAATTTGTGTAC[A/C]TAAGTGGCTTGTTTT	161436
rs191566985	snp	A/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88647296	TTGAACCCAGGAAAC[A/G]GAGGTTGCAGTGAGC	161436
rs191596178	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88631197	ACTGAAAACATATCT[A/C]ATGTATTCAATGCTA	161436
rs191602104	snp	C/G/T	0.00478244	0.0486902	intron-variant	EML5	GRCh38.p7	14:88655279	TGGTACCAAAACAGA[C/G/T]ATATAGACCAATGGA	161436
rs191618935	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653551	TGCATCTATTGAGAT[A/G]ATCATGTGGTTTTTG	161436
rs191717598	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88765067	CAGCATCCAAAGAAA[A/C]AAGTAACATATTAGT	161436
rs191718089	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88762899	AAACTGAACAACCTG[C/T]TCCTGAGTGACTACT	161436
rs191734299	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725799	GCCTACACAAGAGTA[A/C]AATGGTGAGAATAGA	161436
rs191745650	snp	C/G/T	0.000270724	0.0116316	intron-variant	EML5	GRCh38.p7	14:88695478	AATTAATGAGAGAGA[C/G/T]AAACTGACTATTAAC	161436
rs191783789	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786241	CCCAATAGTTTCTAT[C/T]GCATTTTCTCACCTT	161436
rs191787727	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766970	TTTCATAAATTCAAC[A/T]TGTAGGTCATCCTGG	161436
rs191801022	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748593	ATTACAGGTATGTGA[A/G]GAAACAGGAAAATGT	161436
rs191805776	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728344	TTAGAAGCACCAATT[C/T]CCATGCCATCAAAAA	161436
rs191831548	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88688169	CACAGACTACTGCTG[C/G]ATAGTCCAGGCAAGT	161436
rs191835741	snp	C/T	1.76015e-05	0.00296655	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706368	CCACTGATAATCATG[C/T]GACCATCTGACATTA	161436
rs191880943	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679113	TTCCTATATCTTCAC[A/G]TGGCCTTCTTATAAG	161436
rs191912331	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630392	TATGCCAAGTGTATT[C/T]TGTCCTTTAGTCTCT	161436
rs191919493	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703964	CACTTACATAGTGCT[C/T]ATTATGTGCCACATA	161436
rs191948711	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88718244	ATAAGTAACTGGATA[C/T]GCATAGCTCGAGTTT	161436
rs191952341	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88636129	GAACAGCTTGGCCAC[C/T]CCTCAAGAGTATACA	161436
rs191955508	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88640071	ATAGAGAAACCATGA[A/C]TACTACTAGGCCCCC	161436
rs191970402	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88710856	GGTAAAATATTCACA[C/T]AGCAGTTCAAAGAAC	161436
rs191970461	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88660720	TGCACTCCAGCCTGG[C/T]GACAGAGTGAGACTC	161436
rs191979967	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682155	ACCGAATAGTGAGTA[A/C]ATCTATCAAAACTTT	161436
rs191986512	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88788623	GAAAGCAGAGTCAAA[C/T]AACAAAATGCCCCAA	161436
rs192004640	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752393	TTTTATGCTATGAAA[C/T]AGGTATTATTTCCTT	161436
rs192005180	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88782888	AGTTCAAGATCAGCC[A/G]GGCCAACATGGTGAA	161436
rs192016606	snp	C/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88769983	TTTTTTTTTTTTTTG[C/G]TCTTTATCCTTACAG	161436
rs192022740	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746861	GAGGCAACTCATGAA[A/G]AGGGAGAAACACCTC	161436
rs192023831	snp	A/C	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88753788	CTCATAGGAATTGTT[A/C]CATTATATTCAATAA	161436
rs192032217	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731934	TTTTTCTAGTAAATT[C/T]GTTTGAGTTCTTTGT	161436
rs192038298	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88675375	GTGCACCTGCAGGCT[C/T]AACACCACATGGAAG	161436
rs192045295	snp	C/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88617394	TCAGGTGATCACCCC[C/T]GCTCGGCCTCCCAAA	161436
rs192102044	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88789367	TAAACCAGTTACTAA[A/G]ATAAATATAACTAAA	161436
rs192197928	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698835	ATGACTAACACTCAC[G/T]GAGAAGTAATTTATG	161436
rs192198265	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622486	AGTAATGTTGGCAAG[C/T]AAATCCATCGTTATG	161436
rs192200214	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88621969	TACAGAATACTAAAA[C/T]ATACTATTCCTATCT	161436
rs192208253	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88663801	TGGCCTCCCAAAGTA[A/C]TGAGATTACAGGCAT	161436
rs192261350	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775963	AGAGAAATGAGTAAG[A/T]GTGTGCCTGCCTGGT	161436
rs192266054	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88775124	AATACCCGGGTACTA[C/T]GTCAAGGGCCTTAAG	161436
rs192272549	snp	A/G	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614679	GATAGGCTAGACAGC[A/G]AATTCCTGAATGATG	161436
rs192277233	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88759453	CTTTGGGAGGCTGAG[G/T]CAGGAGGATCACTTC	161436
rs192282578	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88737768	ACATGTACTCTTCTT[C/T]CTTCTCCCTTGTAGA	161436
rs192288147	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88658918	GCCTATGTACAGCAT[A/G]AGTATGTTAACAAAA	161436
rs192314742	snp	A/G	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88643836	TCATTGACTTTGTAG[A/G]ACTAGGTTGGGGAGG	161436
rs192316166	snp	C/T	0.000133373	0.0081651	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664517	CCCAATCAATATGGG[C/T]TATGTAACTGGTAGC	161436
rs192333485	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88705035	ACTAATAAAGGTGTT[C/T]GTATACTCCCAATAT	161436
rs192334016	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88769500	TTTCTTTATAGCAGT[A/G]TGAGAATGGACTAAT	161436
rs192352666	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616308	AAAGGCTCTTATTAG[G/T]AACTATAATCTCTAT	161436
rs192501024	snp	A/C/G	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88770477	ACAAGAGACCATTCA[A/C/G]TACAGAGAAAAAATG	161436
rs192502809	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755158	CATGCTAACAGTTAC[C/T]ACTTCATAGAATATG	161436
rs192508224	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692500	TATATTAGGTATTAT[C/T]GGTAGTCTAGAAATG	161436
rs192514590	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88733041	GAAACTTACATTGTG[G/T]TAAAGTCATTTGAAC	161436
rs192515054	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88781286	GGCTCCTAGTAACTT[G/T]CCAGTAGGGTAAAAC	161436
rs192516848	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88763600	GAGCTGGTACCATTC[C/T]TTCCAGAACACTTCC	161436
rs192519797	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732306	CAGTTTTCCCAGCAC[C/G]ATTTATTAAATAGGG	161436
rs192605290	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612402	GGAGGCAGCTGGAAT[A/G]GCAAGTGCAGAAAAT	161436
rs192607384	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643277	ACAAGGTAGTCTGAT[A/T]CCAAGAACTTTAGTT	161436
rs192648596	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675759	TTTATGCTCTGGTTC[C/T]CTTTAAAAACTGAAT	161436
rs192649877	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88644901	TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	161436
rs192665425	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714849	CTTCTTTGATTTCCT[A/G]TGATCAAATGTAACT	161436
rs192728885	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88757991	TCAAGTAGCTGAGAC[A/T]ACAGGTGGGTGCCAC	161436
rs192802201	snp	G/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88790536	AAATCATATCTAGTT[G/T]CAGAAGACCTTAGTG	161436
rs192805221	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669713	GGGATTTCCCCCAGT[A/G]TAATGCACCCCCTCT	161436
rs192807332	snp	G/T	0.000155342	0.00881176	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754583	AAACTGATATGGTCT[G/T]CACAGTGTATGAATC	161436
rs192812357	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88711122	ATCTTAAAATTTGTT[C/G]TGCATGGTGACTCTC	161436
rs192828972	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745057	TAACGGGTCTATTTA[A/T]ATAAATTCCAAATAG	161436
rs192842034	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625754	ACCCAAAATGTTCAA[C/T]TGAAATTTGACATGG	161436
rs192851268	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88668975	ACCAGCAACTGAGGT[A/G]TCCAGGTTCTCTCAT	161436
rs192871683	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88781913	AACGAACTAATTCAG[G/T]AAATTGGTAAAGATA	161436
rs192880391	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623151	CTCCCGAGTAGCTAG[A/C]ATTACAGGTGTGCAC	161436
rs192882275	snp	A/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88696452	GTATTTCAATTCTCA[A/T]CTCTTTCTTTGCTAG	161436
rs192887533	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664930	AAAATGGAACTAAAC[A/C]AACATAAGTAAATTT	161436
rs192927230	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88774297	ACTTTTCAGAAGCAA[C/T]GATCCAGGGCTGCCA	161436
rs192933634	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735651	TAAAATGCACACATC[C/T]TTTGACTACTGCTAA	161436
rs192956614	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88727271	GGTAATGCACATAGC[A/G]GTCAAAATTCTGTCA	161436
rs192991016	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88656271	GCACATAAACACCAC[A/G]GAATACTATGCAGCC	161436
rs192996194	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766559	CTCAAACCCGGTCTC[C/T]TGATGTTACCAATGA	161436
rs193002159	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88697608	AATTCTTAATTATTC[C/G]TCTAGACTCAAGTAA	161436
rs193015356	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88691613	TAGGGGAGAGATTAA[G/T]AAATCATAACTTGAA	161436
rs193041192	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88722912	ACTTAAAATAAAAAT[C/T]AAAATAAAAAAAATG	161436
rs193056850	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88650541	TAGGAAAAACATCCA[C/T]GAAAGTATCAACCAA	161436
rs193062444	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88639123	CAATACAGTACAAGG[C/T]TGAAGATTCCAAGTG	161436
rs193073737	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88681348	GGGGGCCGTGGCTCA[C/G]GCCTGTGATCCCACC	161436
rs193079541	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763890	TTACAGATGCTTTTA[C/T]AGCCGGGTTAAAGAA	161436
rs193109131	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721793	AAACTAAAGAGCTTC[A/G]GCACAATAAAAGAAA	161436
rs193122876	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88791273	ATGCCCAATTTAAAT[A/C]CTGTGCAACATACAT	161436
rs193200834	snp	A/T	0.00636936	0.0560724	intron-variant	EML5	GRCh38.p7	14:88785369	CAAAGGATAAAGCCT[A/T]GAGGGGAAGGATACC	161436
rs193201454	snp	G/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88677507	AACTGTCATCAGAAT[G/T]ATCAGGCAACCTACA	161436
rs193202435	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88716440	AATCCATATACCGTA[C/T]TGCCCTTTGCTCCAT	161436
rs193203748	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748139	TTCAGAGAGGACAAG[A/T]TGCCTAGAATTTGCA	161436
rs193234425	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617188	TTTTCGCTCTTGTTA[C/T]CCAGGCTGGAGTGCA	161436
rs193237723	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660061	CAGGAGGATCACCTG[A/G]GTTCAGGAGTTTGAG	161436
rs193261635	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744410	TAGGACACGAAGGGA[A/G]GTGCTTGCATAATTT	161436
rs193265926	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700594	GAAAAGCATGACTTA[C/T]TACTGCAAACCCATT	161436
rs193277321	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770789	TTAATTTGGGAGACA[A/C]ATGACAGATGTAATC	161436
rs199524770	snp	A/G	0.000215533	0.0103788	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88681963	TAAGGTTTTATCATC[A/G]CTTACAGTAGCACAG	161436
rs199561846	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88660280	GAGAGAGACGCTGTC[-/T]TTAAAAAAAAAAAAA	161436
rs199563602	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88741176	CAAGAAAAAAAAAAA[-/T]TTTAGGTTAAAAAGT	161436
rs199589411	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88749011	AAAAGAAAAAAAAAA[A/C]CTGAAGAAATAATAG	161436
rs199607977	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88749109	GGATAATCATTCACA[C/T]AGAAAAAACACACAA	161436
rs199608985	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88713840	TTGCAAAGTTTATTT[G/T]TTTTTTTTTTTTTTT	161436
rs199620328	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88722974	TTATAGAATCTGTAT[A/G]TAACACAGCAATAAG	161436
rs199621452	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88683163	TGTAAAAAATCTAAT[A/T]AAAAGTAATTGGGAG	161436
rs199662255	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618185	GGATTTTCTAACTGG[C/T]CTTCAAAGTCAGTTC	161436
rs199664529	in-del	-/AACAA			intron-variant	EML5	GRCh38.p7	14:88650458	ACTCTGTCTCAAAAG[-/AACAA]AACAAAACAAAACAA	161436
rs199683965	in-del	-/A	0.0111262	0.0737517	intron-variant	EML5	GRCh38.p7	14:88656617	ACTTAAAGTATAATT[-/A]AAAAAAAAGTGATCT	161436
rs199685835	in-del	-/AAGA			intron-variant	EML5	GRCh38.p7	14:88725964	TTCACTGAGGTAGAG[-/AAGA]AAGACTTCGTAAGTA	161436
rs199700952	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88668434	GAATAAAGTATTTCA[-/G]AAAAAAAAAAGGGAA	161436
rs199701262	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88773818	CATCACCTGGAGGTG[-/A]TAAAAAACTTATTAC	161436
rs199793144	snp	A/G	1.66532e-05	0.00288554	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664528	TGGGTTATGTAACTG[A/G]TAGCTCCTTTGCATA	161436
rs199809774	snp	A/G	0.00090781	0.0212857	intron-variant	EML5	GRCh38.p7	14:88657520	ACAATAAAAATATAC[A/G]AGTAATTCTTTAAGC	161436
rs199810358	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680628	AGTACTAGCTTTCAA[A/G]TTTTTATGTTAATTT	161436
rs199823881	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88760343	GTAATGTAGGTTATA[G/T]TTGTTTGTTTGTTTG	161436
rs199826547	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88689323	TGTTTTCCGAAGTTT[A/T]TATACCAATGTACAC	161436
rs199829513	snp	A/G	4.97541e-05	0.00498744	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626873	GCATGGTCTGCATCC[A/G]GGCATCTTCCAGTGT	161436
rs199872585	snp	A/G	0.00188231	0.0306204	intron-variant	EML5	GRCh38.p7	14:88726518	AGATAAAATTATTAT[A/G]TGTTTCTACCCTAAT	161436
rs199895449	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88773825	TGGAGGTGATAAAAA[A/C]CTTATTACTGGGGCC	161436
rs199922256	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88780384	ACAAAGGGTAGATTT[G/T]TTTACTGTTCAGTAT	161436
rs199924646	snp	C/T	1.67083e-05	0.00289031	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740418	ATTGTTCGTATAAGA[C/T]TGATTCCTTTCCAAA	161436
rs199943269	snp	A/C	0.000281501	0.0118605	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688405	CAGTCCATCCATACA[A/C]TGCACACATCATTGT	161436
rs199946782	in-del	-/TC	0.0486741	0.148216	upstream-variant-2KB	EML5	GRCh38.p7	14:88793280	ACCGGGATGCTAAAT[-/TC]TCTTTTTTACGCTTG	161436
rs199997066	in-del	-/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88697744	TTTATTTATTTTTTA[-/T]TTTTTTTTGAGATGG	161436
rs200009435	snp	C/T	0.0011411	0.0238589	intron-variant	EML5	GRCh38.p7	14:88705632	TGTTTAAAGAAGATT[C/T]ATTTTCAAAACAGCA	161436
rs200010274	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88742285	CTTTCCAATACAGTA[A/G]CCACTACTAGATACA	161436
rs200040306	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88684450	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	161436
rs200045403	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88738418	GAGAAAAAAAAAAAA[-/A]TCCCCCAATTGCTGA	161436
rs200046870	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88695214	AAATCATTTACTATG[A/T]TTATATTATTTATTC	161436
rs200107954	snp	C/T	0.000248597	0.0111462	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626883	CATCCGGGCATCTTC[C/T]AGTGTGCTCAGTAGC	161436
rs200116313	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88777250	CAGAAGACTTTACAG[G/T]GGAAACCTTACAAGC	161436
rs200209147	snp	C/G	0.000282394	0.0118793	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616287	CATTTGGTGCACACA[C/G]AAGTCAAAGGCTCTT	161436
rs200233124	snp	C/T	9.93641e-05	0.00704785	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688429	TCATTGTGTCATTTT[C/T]CCCCAGTGTGCCTAT	161436
rs200252116	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88624858	AGAAGCATATGAGGA[A/G]GAAGGTCGGAGAGGA	161436
rs200260341	snp	C/T	0.000155666	0.00882094	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618795	CCTACTGCCAGATAC[C/T]GGGAATCCGGACTAA	161436
rs200269877	in-del	-/CTA			intron-variant	EML5	GRCh38.p7	14:88684186	TATGCAATCAAAATT[-/CTA]AAGAAAACAGTTGTA	161436
rs200274572	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88712095	TCTAATAAAACTTCA[C/T]GACCAAAATAAATGC	161436
rs200298326	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88699658	AGCATTGATTGTCAG[C/T]AGAGATATGGAAAAA	161436
rs200299305	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765458	TCTTCCAATCAGCAA[C/G]GGCACATTGAGTTCT	161436
rs200321497	in-del	-/A	0.0185938	0.0946107	intron-variant	EML5	GRCh38.p7	14:88673081	ATGCAACAAAAAAAA[-/A]GAAAACTCCAGGCCA	161436
rs200329420	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88658975	ACACATATATTTATA[C/T]ACCCATGTAAATATC	161436
rs200341196	in-del	-/CAA/CAACAA			intron-variant	EML5	GRCh38.p7	14:88717788	CAACAACAACAACAA[-/CAA/CAACAA]AACAAATTAAAGGAG	161436
rs200361077	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88647687	AGAGTGAGACCGTCT[A/C]AAAAAAAAAAAAAAA	161436
rs200365238	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88747892	TACCCTCCCCGACCC[A/C]CCCCTGCCATAAACA	161436
rs200380112	snp	C/G	0.000137544	0.00829176	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661817	GTCCATGATGCCCAA[C/G]CAATTTTTTCTACCT	161436
rs200411307	in-del	-/A	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88774539	GATTACAATATAATT[-/A]ATAGCAAAACTTCGC	161436
rs200426672	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88745171	AAATTGTGTGTTTGT[G/T]TGTGTGTGTGTGTGT	161436
rs200451209	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88792759	GATGCCCAGAGCCCT[C/T]CGCCCGCCTCGGCTC	161436
rs200473832	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88622943	ATTTTGAGAAATACT[C/G]TTTTTTTCTGACATG	161436
rs200490283	snp	A/T	8.36043e-05	0.00646492	intron-variant	EML5	GRCh38.p7	14:88746164	CAGTACTCATTAGAA[A/T]TCTCAAAAGAGAATA	161436
rs200518597	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88653921	CGAATCCATCTGGGC[-/T]TTTTTTTTGGTTGGT	161436
rs200521006	in-del	-/CATTATTCT			intron-variant	EML5	GRCh38.p7	14:88706770	ACTAGACCTTACCCC[-/CATTATTCT]CAACCCAAGCAGCCA	161436
rs200560737	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88701922	GAATCTATAAACATC[A/C]TTTCTTCCCTTCCTT	161436
rs200566698	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88678453	AAAATAACATAAAAT[-/A]AAAAAAAATTTTAAA	161436
rs200580153	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88777247	TGGCAGAAGACTTTA[A/C]AGTGGAAACCTTACA	161436
rs200585166	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660745	AGACTCCATCTCAGG[A/G]AAAAAAAAAGAAAAA	161436
rs200604070	snp	G/T	0.00299557	0.0385851	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615826	GCATCTCTCAGTGAG[G/T]TGTATGTACACATTT	161436
rs200608863	snp	C/T	6.70837e-05	0.00579114	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704861	TAGTTGTTTTATACC[C/T]GTGAACAAAGTGTAA	161436
rs200625871	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768557	CTGGAATTACAGGTG[C/T]CCGCCTCCACACCTG	161436
rs200661206	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88712496	CTCCTAAAAATAAAT[A/C]AGAGTCTTAATTTAA	161436
rs200722411	in-del	-/CTTC			intron-variant	EML5	GRCh38.p7	14:88689570	TTCCTTCCTTCCTTC[-/CTTC]ATTCAAGAAATATAT	161436
rs200753157	snp	G/T	1.74885e-05	0.00295701	intron-variant	EML5	GRCh38.p7	14:88681877	TCTACGTTCAAGTGT[G/T]AGAGCCTCTTACCCT	161436
rs200761896	snp	A/G	3.32143e-05	0.00407505	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622672	TGAAGGCACGGCACC[A/G]CCTCAGTTCCTGATC	161436
rs200767163	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88760480	ACCATATCTATATTA[A/C/T]TTTTCCACAAATTGC	161436
rs200779861	snp	A/G			utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88614324	CAAGTACCAACTTAC[A/G]TTTCAAGCTTCTTAG	161436
rs200798066	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88729565	CTTATTTGGTTTTTT[-/G]TTTTTTGTTTTTTTG	161436
rs200798359	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761436	ACTCCCACTTACAAG[C/T]GAGAACATGTGGTGT	161436
rs200811130	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687683	TGGTAACTACCTGAT[A/G]GATATGGTGATTATA	161436
rs200820604	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88662559	TTTTTTTTTTTTTTT[-/A]TAATACAGGGTCTCA	161436
rs200826655	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703918	TACATATGAAACTTT[C/T]ATAAGACAAATTTAT	161436
rs200857460	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88781464	CAGAATAACAATACC[A/G]ATGATACTACCACTA	161436
rs200868411	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88787355	AAACAGAAGCTCAAC[A/G]AATATTTCTTGGATG	161436
rs200870978	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88676422	CCATCAGAAGTCATT[A/C]GACTCACTATCACGA	161436
rs200896608	snp	C/T	0.000140804	0.00838941	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88695453	CAAACGTTTCCCATC[C/T]GCTGTGGAAAATTAA	161436
rs200898520	snp	A/C			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767883	CTAAAAACCTTATTC[A/C]AAAATTCACCATTTT	161436
rs200908814	in-del	-/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88635501	GGACAGAAGTACAAA[-/T]GAAAGCTTGAATGTC	161436
rs200948540	in-del	-/TGTG			intron-variant	EML5	GRCh38.p7	14:88745168	TCTAAATTGTGTGTT[-/TGTG]TGTGTGTGTGTGTGT	161436
rs200973480	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88769982	TTTTTTTTTTTTTTT[A/C]GTCTTTATCCTTACA	161436
rs201021105	snp	G/T	0.0013057	0.0255176	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661767	CTTCTCCAATTACTG[G/T]CCAAATTCCTTCACA	161436
rs201039602	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88741164	AGACTCCGTCTCAAG[-/A]AAAAAAAAAAATTTT	161436
rs201072176	snp	C/T	0.00257434	0.0357847	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88754530	TCCATCTAAGTCAAA[C/T]GCCAAGCAAGCTATA	161436
rs201076743	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88664291	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGGAAA	161436
rs201082818	in-del	-/GTC	0.0232847	0.105357	intron-variant	EML5	GRCh38.p7	14:88651246	CCCTCCCCACACCTT[-/GTC]GTCATTTTCAAAATA	161436
rs201139712	in-del	-/AAG			intron-variant	EML5	GRCh38.p7	14:88640988	GTGGGCCTCTAAAAA[-/AAG]AAGAAGAAGAAGAAG	161436
rs201160406	snp	A/G	3.31334e-05	0.00407009	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88736539	GAATGTGGTCACCTC[A/G]CCAACACACACTCCT	161436
rs201171773	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88675346	AGGTTCCCAAACCTC[A/G]ATTCTTGACTTCTGT	161436
rs201176843	snp	A/G	5.02694e-05	0.0050132	intron-variant	EML5	GRCh38.p7	14:88644530	CAACAGAGAAGTGGG[A/G]AGGAGGAAAGGCATG	161436
rs201187413	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732370	TGTCAAAGATCAGAC[A/G]GTTGTAGATGTGTGG	161436
rs201204486	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88769967	TTTTTTTTTTTTTTT[-/T]GGTCTTTATCCTTAC	161436
rs201231006	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782807	TGCCTGGATCGGGCA[C/T]GGTGGCTCACATCTG	161436
rs201236117	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660748	CTCCATCTCAGGGAA[A/G]AAAAAAGAAAAAAGA	161436
rs201245817	in-del	-/GTC			intron-variant	EML5	GRCh38.p7	14:88712619	AAATACATAAATAGG[-/GTC]TAGATAAGTTTGGGT	161436
rs201270690	snp	A/G	0.000266821	0.0115473	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740388	TTAAATGTACTTACA[A/G]CATGGGCTCCTTGTA	161436
rs201280266	snp	A/G	0.000729794	0.0190883	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665434	TAAGAAGCTTCCATC[A/G]TTGAGACCTACGGCT	161436
rs201281131	in-del	-/AAAAC			intron-variant	EML5	GRCh38.p7	14:88778778	CAAGACTCCATCTCA[-/AAAAC]AAAACAAAACAAAAC	161436
rs201284523	in-del	-/ATTTT	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88622923	ATCCAGTTTCAGTGA[-/ATTTT]ATTTTGAGAAATACT	161436
rs201305947	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88691203	CACACTAGGATCTAT[A/G]TGTCACTGGGGTAGT	161436
rs201337507	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88739777	AATGAATAAAGGAAA[A/G]AAAACCAATTCAACA	161436
rs201339176	snp	A/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767887	AAACCTTATTCAAAA[A/T]TTCACCATTTTTTCC	161436
rs201348611	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88700308	AATTTCTTTTTTTTT[-/A]AATTGTTTTATTTGG	161436
rs201389267	snp	C/G	0.0114555	0.0748099	intron-variant	EML5	GRCh38.p7	14:88694259	AATTACTTTCAAAAG[C/G]AATAATTTCTTAAAA	161436
rs201391375	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774955	AGTTGCTTGGTCAAA[A/G]TCATGAGGCCCCTGT	161436
rs201392863	in-del	-/CT	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88659237	CCCTAGGAATGACGA[-/CT]CTCTTTTTTTTTTTT	161436
rs201405202	snp	A/C	0.0018881	0.0306674	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621161	ATCTTCTGCAGCAGA[A/C]AGGAAAAAATCCCTG	161436
rs201466730	snp	C/G	0.00570609	0.0531082	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615772	TGGTTTTTCTTCTCT[C/G]TAATTCTGGTCTCAA	161436
rs201517219	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760342	TGTAATGTAGGTTAT[A/G]GTTGTTTGTTTGTTT	161436
rs201532947	in-del	-/T	0.00795532	0.062565	intron-variant	EML5	GRCh38.p7	14:88650630	TTTAATTGTTTTTAA[-/T]TTTTTTTTCATTTAT	161436
rs201540048	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88674819	TTACTTCCTAGATAC[-/A]ATGGGGGTACAGGCA	161436
rs201541273	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766384	GAGAAAGAGAATGTG[G/T]TCCCAAGGGGAGGTC	161436
rs201544875	in-del	-/T	0.0298908	0.118541	intron-variant	EML5	GRCh38.p7	14:88656615	GAACTTAAAGTATAA[-/T]TTAAAAAAAAGTGAT	161436
rs201547990	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613687	AATGAGCATGGTTGG[C/T]GATTGGAAGCAAGGG	161436
rs201557770	snp	C/T	0.00249513	0.0352326	intron-variant, utr-variant-3-prime, synonymous-codon	EML5	GRCh38.p7	14:88616111	AACTAGTAACATAGT[C/T]TGCTCTTCATGGGCT	161436
rs201558061	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88720147	TGAGGCAGTAATAAA[C/T]AGCCTACCAACCAAA	161436
rs201595964	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660299	AAAAAAAAAAAAAAA[C/T]AAAGGAATGCATTGT	161436
rs201625686	snp	A/G	0.000349368	0.0132122	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618273	ATAGCGGCATGATCC[A/G]TAAGATGTTTTCCTG	161436
rs201634745	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88753473	TATAAAACTAATTTT[A/T]TGAATTAAAAAGCAG	161436
rs201647289	snp	A/G	5.06222e-05	0.00503076	intron-variant	EML5	GRCh38.p7	14:88644414	ATTTCAGTAACACTG[A/G]AGAGTGAGTTTTCCT	161436
rs201667400	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88729568	TTTGGTTTTTTGTTT[-/G]TTTGTTTTTTTGAGA	161436
rs201738161	in-del	-/GT			intron-variant	EML5	GRCh38.p7	14:88745168	TGTGTGTGTGTGTGT[-/GT]AATAGGCCTCTCTGT	161436
rs201768125	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618608	CACGAAATGTAAAAG[A/C]AGAAGAACTTGCCAC	161436
rs201785678	snp	A/G	0.000839701	0.020473	intron-variant	EML5	GRCh38.p7	14:88687366	TTAATAAAGATCTAA[A/G]TATTTTTTAAAATAG	161436
rs201789081	snp	A/G	1.67668e-05	0.00289537	intron-variant	EML5	GRCh38.p7	14:88658167	CTATATTTTTGTTCA[A/G]GTATTATAAAATGAC	161436
rs201840869	snp	A/G	8.34815e-05	0.00646017	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665408	TCCTCTAGAGTATCC[A/G]CATTTGCCATTAAGA	161436
rs201845710	snp	C/T	0.000222891	0.0105544	intron-variant	EML5	GRCh38.p7	14:88744112	AACAAATCAGATTCA[C/T]GATTAAAATACTTAT	161436
rs201867495	snp	C/T	0.000463364	0.0152141	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706261	GCATACTACTCACCT[C/T]GGGGTGCTATGTGAA	161436
rs201879199	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88659253	CTCTTTTTTTTTTTT[-/T]GATACTGGAATGCAG	161436
rs201884924	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88620935	ACATCTTCTGCATTT[-/A]AAAAAAAAAAAAAAA	161436
rs201922439	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88771401	CCTTGAACTCTCCGC[A/T]TGTGTTCTAGGTCCC	161436
rs201924936	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675378	CACCTGCAGGCTCAA[C/T]ACCACATGGAAGCTG	161436
rs201928279	in-del	-/A	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88687755	ATGAAGTTAAACTTT[-/A]AAAAAAAAACAAAAA	161436
rs201934962	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88780739	CGCCATCATGCCCAG[A/C]TAATTTTGTATTTTT	161436
rs201948547	snp	C/T	0.000965476	0.0219501	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712367	CATCTACTGAATTTA[C/T]ATCGTTGATATCTGA	161436
rs201953300	snp	C/T	8.38849e-05	0.00647576	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642924	CAGAATTCCAACAGA[C/T]GCAGTGTGATAAATT	161436
rs201995205	in-del	-/TAGT	0.0376037	0.131863	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613406	TATCATTTATAAAGA[-/TAGT]TTTGTTCTCAGTTTC	161436
rs202003213	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695213	GAAATCATTTACTAT[A/G]ATTATATTATTTATT	161436
rs202034373	in-del	-/AAGGAAAAA			intron-variant	EML5	GRCh38.p7	14:88664308	AAGAAAAAGGAAAAA[-/AAGGAAAAA]GAAAAGTCTCAACTC	161436
rs202053644	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88720281	CTCCTCCCTAACTCA[-/T]TTTATGAGGCCAGCA	161436
rs202124674	snp	A/G	3.39058e-05	0.00411725	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696872	AACGGCACTAACACC[A/G]TACTGGTGGTGGCCC	161436
rs202138048	snp	C/T	0.00299545	0.0385843	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688401	TCTTCAGTCCATCCA[C/T]ACACTGCACACATCA	161436
rs202152562	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88658079	GACTAAAAACAGTAC[C/T]ACTACAATTATTCAA	161436
rs202187448	snp	A/G	0.101658	0.201233	intron-variant	EML5	GRCh38.p7	14:88732087	AGATCCCATTTGTCA[A/G]TTTTGGCTTTTGTTG	161436
rs207475124	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88758707	AAAACATATGTCCAC[A/T]CAAAACTTGTACACA	161436
rs207475125	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88770676	CATGAGTGTTGTTCA[C/G]GTATCCTTCAGGTTA	161436
rs267604080	snp	C/T			synonymous-codon, missense, nc-transcript-variant	EML5	GRCh38.p7	14:88622703	CCACAGTTTAACCGC[C/T]CCTCCTTCTTTTGAC	161436
rs267604081	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740425	GTATAAGATTGATTC[C/T]TTTCCAAACATATAT	161436
rs367572806	snp	A/T	0.000248252	0.0111384	intron-variant	EML5	GRCh38.p7	14:88694262	TACTTTCAAAAGCAA[A/T]AATTTCTTAAAATTC	161436
rs367574928	snp	C/G	0.000167986	0.00916322	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657491	TCTCCCTTGTAACAT[C/G]ACTGTCATAGCCTAC	161436
rs367660901	snp	A/G	0.00020305	0.0100739	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618695	CATTTGAATGACAAA[A/G]CTTGGAATGTCTTTG	161436
rs367664333	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88686460	TCTGGGCCCACAGCC[C/T]GGAGGATGGTCGGCG	161436
rs367669714	in-del	-/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626733	GGGCATGTAATGATT[-/T]AGCAGATCACAGTAT	161436
rs367685483	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88709773	GACCCAAATGTCCAA[C/T]GACAGGAGAATAAAT	161436
rs367685695	snp	A/G	0.000132481	0.00813775	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688311	ACTGGCCCATCATGC[A/G]CTTTCACTGTTTTTA	161436
rs367696128	snp	C/T	1.67494e-05	0.00289386	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702507	AGAATATCATCATCA[C/T]GACCCAGATAAAAAC	161436
rs367746746	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88717546	GGCAGATCACAAGAT[C/G]AGAGAGAGACCATCC	161436
rs367752954	snp	C/T	0.000265243	0.0115131	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740448	ACATATATATCCCCA[C/T]TGAGTGCACCAGAAT	161436
rs367753152	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692436	CTTTTTTTCCTTGTC[A/G]TTATTCCCTAAACAA	161436
rs367767836	snp	A/G	0.000352144	0.0132645	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88663064	TTGTTTTTTCCCTCT[A/G]GGAGCTTCAAAGAAT	161436
rs367776388	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88763886	GTTTTTACAGATGCT[G/T]TTATAGCCGGGTTAA	161436
rs367783342	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88731450	ATATGTGCCACATTT[G/T]CTTAATCCAGTCTAT	161436
rs367787484	snp	C/T	0.000149045	0.00863135	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88736447	TTCACCTTCACAATG[C/T]CCTTGCATAATTAGA	161436
rs367808154	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88723952	TCCAACTCTAACATA[A/T]CCCCCACTCCTGGTG	161436
rs367809451	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760448	CTTCCCCAAGCACTT[C/T]TGTCAAAAATCAATT	161436
rs367815016	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747041	ATATAAATCCTAAAT[A/G]AAGTACCGCAACTTT	161436
rs367868445	snp	A/G	0.0329836	0.124112	intron-variant	EML5	GRCh38.p7	14:88734910	ATATCAGCAAACGCA[A/G]TATATGAAGCTCATT	161436
rs367904800	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88662946	GAACAGACTTCACGT[A/G]TAACTAAACGATAGA	161436
rs367936873	snp	G/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612039	GCACTGCTGTTGTGA[G/T]GATCAGCATATGAAA	161436
rs367940184	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713220	AATATGGTAAAACTC[C/T]ATCTCTACTAAAAAT	161436
rs367949027	in-del	-/AAG	0.00993419	0.0697739	intron-variant	EML5	GRCh38.p7	14:88670876	TTAGAGAAAAAAAAA[-/AAG]GATGAAAAGGAATGA	161436
rs367973056	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88777091	CAAGTACAAGAAGGA[G/T]ATAGAACACCAAGCA	161436
rs368030783	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623087	GTGGCATGATCTAGG[C/T]TTATTGCAACCTCTG	161436
rs368055942	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88691230	TAGTGAAGCTCACTA[A/C]AGTTTCACTCCCAAC	161436
rs368062275	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88644934	CCAGGCTGGTCTCGA[A/T]CTCCTGACCTCAGGT	161436
rs368109589	snp	A/T	4.14293e-05	0.00455115	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687258	TTTTTATAGCATAGG[A/T]CTTGAGACATCTTTC	161436
rs368112776	snp	C/T	0.0013	0.0254619	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88622704	CACAGTTTAACCGCT[C/T]CTCCTTCTTTTGACC	161436
rs368115923	snp	C/G	6.55931e-05	0.00572645	intron-variant	EML5	GRCh38.p7	14:88744099	TCAAATATCTGTAAA[C/G]AAATCAGATTCATGA	161436
rs368134263	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88632191	ATACGCCCATACCCA[A/G]TTAATCAGAAAGGAT	161436
rs368135566	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679965	TTCAACTCAATAATA[C/T]TATCATTAATAAACT	161436
rs368140827	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88655962	CATTAAAAAGTCAGG[A/C]AACAACAGATGCTGG	161436
rs368142940	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666972	GTGGCAGCAGTGGAG[A/G]TGATAAGAGGAAGGA	161436
rs368146750	in-del	-/TGAA			intron-variant	EML5	GRCh38.p7	14:88661936	GTGTCACAAGTAAAA[-/TGAA]AGTTTTAATGAAAAA	161436
rs368150464	snp	A/G	8.32328e-05	0.00645054	intron-variant	EML5	GRCh38.p7	14:88658183	GTATTATAAAATGAC[A/G]TACCCCCATCTTCTT	161436
rs368188593	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642581	GAGGTTATGGGAAAA[C/T]AGAATTAAAGTTACA	161436
rs368192765	snp	A/G	0.000167986	0.00916322	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642903	CCTACCTGTAGCAAC[A/G]TTGTGCAGAATTCCA	161436
rs368207168	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715368	GTTGCTGAACAGAAA[C/T]ACATGGAAACAATAT	161436
rs368243006	snp	A/C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88650211	TAATCCCAGCACTTC[A/C/G]GGAGGCTGAGGTGGG	161436
rs368243505	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88711959	AAAAAAAAAAAAAAA[A/T]ACAACCATCATTGTA	161436
rs368258230	snp	A/G	0.000995504	0.0222881	intron-variant	EML5	GRCh38.p7	14:88695505	TAACATTCAGAAGAG[A/G]GAAAACATTCAGTAT	161436
rs368279481	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88714812	TAGAAAAGTCTACAA[C/T]GCCTGAAATATTAGC	161436
rs368280496	in-del	-/TA			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768045	GGAACTTTTGAAGAA[-/TA]CTAACCAGTTATTTT	161436
rs368308406	snp	C/T	5.01953e-05	0.00500951	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665405	AGATCCTCTAGAGTA[C/T]CCGCATTTGCCATTA	161436
rs368314652	snp	G/T	1.67756e-05	0.00289612	intron-variant	EML5	GRCh38.p7	14:88736582	TAGTAAAAAGTAAAT[G/T]GTATTTAATATATAA	161436
rs368321898	snp	C/T	1.67464e-05	0.0028936	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706327	CACTGAAAGACAGAG[C/T]GATCTGCTCCACCAA	161436
rs368323127	snp	C/G	2.6294e-05	0.00362578	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657450	AATATTTGTTGATAA[C/G]GCTCTGATGGTGTAA	161436
rs368346662	in-del	-/CGTT			intron-variant	EML5	GRCh38.p7	14:88760352	TTATAGTTGTTTGTT[-/CGTT]TGTTTGTTTTTTGCT	161436
rs368416041	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88679529	AAACTCCATCTCTAC[C/T]AAAAATACAAAAATA	161436
rs368423826	snp	A/G	4.98451e-05	0.004992	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624993	CTTTCCCCCAGTCAC[A/G]ATAAGTCCATCTCGC	161436
rs368430035	snp	A/C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679169	CAACCAAATCTAGTA[A/C/T]GCCTTTGTCTTAAAC	161436
rs368461118	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691805	CTCTGTGGATCAGAA[C/T]CCCAAAAGTAAGGAA	161436
rs368470651	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88696549	CCAGCGTGGGAGATG[C/G]AAACCACCTGTGGTA	161436
rs368519322	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698993	TAATTTGCCAGTAGC[A/G]AATAAGTGGAAAGGC	161436
rs368549949	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88791200	CAACTTTATTTGTGG[A/C]ATTTACATACCAGGG	161436
rs368586142	snp	C/T	0.000132912	0.00815098	intron-variant	EML5	GRCh38.p7	14:88688246	ACAAATTTTGTTTAA[C/T]TTAAAATCTCTTTAG	161436
rs368605740	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88674462	CAAACAGGTGAAATC[C/G]CAGACACATAAAACC	161436
rs368607277	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88741157	GCAGAGTGAGACTCC[A/G]TCTCAAGAAAAAAAA	161436
rs368608013	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88735714	ATGACAAATGTATAA[A/C/T]GATATTCACTGCAAG	161436
rs368610038	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88784104	TTTCTTGAAACAAAT[A/G]TAAGTGGAAACAACA	161436
rs368615515	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88629781	AACTCAGAGCTGGGA[A/G]AGGCAGCACAGGTAT	161436
rs368645466	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727976	AAGACAAAGATGAAC[C/T]CTTAATGATTTGTTA	161436
rs368659976	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719644	ACTTTAAAATATTTG[C/T]AAGTTTTCATATGAC	161436
rs368692457	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88645061	AGACCAAGTTTCACT[C/T]TGTCACCCAGGCTGG	161436
rs368698114	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791955	TTAAGAATGCGTTTA[A/G]TAAGAAATTTCTCAC	161436
rs368699099	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88708335	CTGTGATTACCCCTT[C/G]TGATTATATTTATAT	161436
rs368705792	snp	C/T	0.0103295	0.0711199	intron-variant	EML5	GRCh38.p7	14:88772835	ACTACACTCCAGCTA[C/T]ACTGGCCTTTCTATC	161436
rs368713545	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88730386	GAAGTAAGTTTCTGA[A/G]TGGTTGATTTGTTAG	161436
rs368713975	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88693019	TACTATTTAGAAAAC[A/T]GACATTTTTTATTTT	161436
rs368730757	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88674772	GGCAAGTCCCTTCCA[A/C]CTATGAGCTTGTAAA	161436
rs368741166	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88735687	TATCAGAGATATTCA[C/T]ACATGTACAAAATGA	161436
rs368745841	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687978	CAAGAGGCTGAGGCA[A/G]GAGGATTTCTTGAGC	161436
rs368748945	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713962	CCCATCCCGACCTCC[C/T]GAATAGCTGGGACCA	161436
rs368772417	snp	C/T	0.000116105	0.00761832	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626872	AGCATGGTCTGCATC[C/T]GGGCATCTTCCAGTG	161436
rs368790601	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663758	CAGGCTGGTCTCAAA[C/T]TCCTGGGCTCAAGCA	161436
rs368799219	snp	A/G	8.42708e-05	0.00649063	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621123	CTTACTTTATCAGCA[A/G]TATCCCAAAGTCTCA	161436
rs368825758	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88786429	CTCTAGTGATAAGAA[C/T]AGTCTTTGGCAAATA	161436
rs368882298	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88695956	ATAATGAATATATTA[C/G]ACAAATCACTGCGAC	161436
rs368905674	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88624010	GTGTTTAATTAACAT[-/AT]GTGGGTTCTTTCAAT	161436
rs368925393	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88697805	CAATGGCGCTATCTC[A/G]GCTCACCGCAACCTC	161436
rs368932434	snp	A/G	4.17894e-05	0.00457088	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715126	AGCAAGGTAAGTTCC[A/G]TCTGGTGAATATTTT	161436
rs368933633	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786301	ATATACATGCATATA[C/T]AAAAATTTACACACA	161436
rs368937046	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88619822	GGCGCCTGCCACCAC[A/G]CCCGGCTGATTTTTG	161436
rs368972507	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88672860	TTGAATCCCTGAATA[A/G]ACCAATAACAGTTCT	161436
rs369015462	snp	C/T	1.76943e-05	0.00297436	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740389	TAAATGTACTTACAG[C/T]ATGGGCTCCTTGTAT	161436
rs369042306	snp	A/C	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88640836	TTAACAAAAAAAAGA[A/C]GATCCCAATAAACAC	161436
rs369049029	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88700320	TTTAAATTGTTTTAT[C/T]TGGGAAAAGTGCTTC	161436
rs369060524	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88650775	CCTGAGTAGGAACCT[C/T]CTGGTACAGGCATGT	161436
rs369071347	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88730458	TCATTTTGAATTGCA[C/G]CAGCTTAAGAAATAT	161436
rs369084384	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88647325	GCCAAGACTGCATGC[A/G]CCACTGCACTGCAGC	161436
rs369138088	snp	A/G/T	3.31566e-05	0.00407154	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658355	TGACATGTGTACTAT[A/G/T]GGCCACATACCTCTT	161436
rs369165040	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769010	GAGCAATATCATCTC[C/T]GAAGGGGCAAAAATT	161436
rs369169476	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88724789	ATTTATTATTTCTAA[C/T]CTGCAAAACTGAAGA	161436
rs369170867	snp	C/G	0.000198985	0.00997261	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88681951	ATCCCATATTCTTAA[C/G]GTTTTATCATCGCTT	161436
rs369195779	snp	A/G	0.000309784	0.0124417	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661693	CACAAATCCCAAATC[A/G]TCCCCGGTAGCTAGA	161436
rs369220629	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88707741	GTTATTTTAGGAATA[A/C]ATTTTTTATGTAGCT	161436
rs369239475	in-del	-/TGAT	0.0103295	0.0711199	intron-variant	EML5	GRCh38.p7	14:88716797	GAGATTGTGGTTGAC[-/TGAT]TGATTGGTATTTTAG	161436
rs369245748	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88625878	AAACAAAAAATGCAC[C/T]TAGTTTTTCGATGCA	161436
rs369265225	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770306	TATAATTTTACTTTT[C/T]ATAATTCATGCTTTT	161436
rs369266735	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88714459	TGAATAAATTCAGAA[A/G]ATCTAATATACAGCT	161436
rs369270571	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88692445	CTTGTCATTATTCCC[C/T]AAACAACAGTACAAC	161436
rs369274426	snp	A/C	0.000328235	0.0128066	intron-variant	EML5	GRCh38.p7	14:88665306	TGCCAGACCCAAGTT[A/C]ATACTCAAATACAAT	161436
rs369324194	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88724403	GACCATTTTGTGAGT[C/T]AGAATTTTGTGGTTC	161436
rs369341061	snp	A/G	6.62449e-05	0.00575483	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688421	TGCACACATCATTGT[A/G]TCATTTTTCCCCAGT	161436
rs369341388	snp	A/G	8.28301e-05	0.00643492	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626910	TAGCCCTTTTTTGCT[A/G]AGAAGAGCTCTTCCT	161436
rs369350892	snp	C/T	1.66048e-05	0.00288134	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616193	TCACCACTGGTAAAT[C/T]GAATATTTGTCACAT	161436
rs369364849	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88660033	GTAATCCCACCACTT[A/T]AGGATGCCGAGGCAG	161436
rs369365669	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88694541	TCTCAGGTTTGGGCT[G/T]TGTATTTGTTCTTTT	161436
rs369370403	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88720932	CTCCAGCAAAGTCTC[A/G]GGATATAAAATCAAT	161436
rs369392931	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88645440	AATATTTCTTGATAG[A/G]TACATTAACAACAAA	161436
rs369429196	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88754902	TCCATCCCGCCAAGT[C/T]CAAGCAATTCTTGTG	161436
rs369442522	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780483	AATACATACAAATGG[A/G]TTTATTTCAAGGAAT	161436
rs369498805	snp	C/T	3.45543e-05	0.00415643	intron-variant	EML5	GRCh38.p7	14:88740583	CAGAACTAAAAGGTA[C/T]ATAGTATAATCAAAT	161436
rs369510704	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88702129	TAGGTAACTCAACCT[A/G]AAGACACCAGATTTC	161436
rs369541080	snp	C/T	1.65762e-05	0.00287886	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658259	GATAGCCTTCCATCT[C/T]ATTTGTCCACACCAT	161436
rs369542815	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88636630	TGTGCCACTGCACTA[C/T]AGCCTGGGCAACAGA	161436
rs369547219	snp	A/G	0.000100839	0.00709994	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715063	GCCAACTTTTTTATA[A/G]CGCTGAGCAACTCCA	161436
rs369549239	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88779754	TGAATTTTAAGACCA[C/G]AGTCTGGGACTTGCT	161436
rs369551011	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88759805	GAAAAAGGATAGGGT[A/G]GGTCCGTGTTTAGAT	161436
rs369575837	snp	A/G/T	3.31231e-05	0.00406948	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621263	TTTCTCTCCAACTTC[A/G/T]ATTATTTCAGCATTC	161436
rs369583025	in-del	-/GAGA			intron-variant	EML5	GRCh38.p7	14:88775921	AGAGAGAGAGAGAGA[-/GAGA]CTCCATTTGTTTGGG	161436
rs369587147	snp	A/T	1.69003e-05	0.00290687	intron-variant	EML5	GRCh38.p7	14:88704854	TGAAAGATAGTTGTT[A/T]TATACCCGTGAACAA	161436
rs369600644	snp	C/G	0.000167986	0.00916323	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615783	CTCTGTAATTCTGGT[C/G]TCAAAGTTAATTTCT	161436
rs369608013	snp	A/G	1.65726e-05	0.00287855	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88627011	CTGCCACAAAAATAC[A/G]TTGATTGTGACCAGC	161436
rs369630879	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88770232	GGTTACTTACTACAT[A/C]CCTGCCATTGTCTTC	161436
rs369672819	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88688875	CATCTCCCTTCTTCA[C/T]GCTTTAGTATTGTGA	161436
rs369713831	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88657972	TTATTTAAAATTCAG[A/G]TATTTTTCATTTGTA	161436
rs369731084	snp	C/T	4.99654e-05	0.00499802	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704878	TGAACAAAGTGTAAT[C/T]GAATACTATTTCCTG	161436
rs369731227	snp	C/T	0.000437904	0.0147905	intron-variant	EML5	GRCh38.p7	14:88646884	GTATCCCATTAATGC[C/T]AAATATGGAAGATGA	161436
rs369750451	snp	C/G/T	3.31742e-05	0.00407262	synonymous-codon, missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644478	GTTTGTCTGGAGTTT[C/G/T]TCTGGCTGTGGTGGG	161436
rs369766326	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793556	TGTTTTGCTTTGTTT[C/T]TAAGTTTATTTTGTA	161436
rs369822404	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88708457	TATCTCTGGTGCCTG[C/G]TATATAGCAAACACT	161436
rs369825301	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88664753	AATTATAATAAAACA[C/G]ATGTGTTAAATAACA	161436
rs369839785	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786998	CAACAAGAACTGCTA[C/T]GGTGAAACAGAACAA	161436
rs369891759	snp	C/T	1.74784e-05	0.00295616	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754591	ATGGTCTGCACAGTG[C/T]ATGAATCCCAAATAC	161436
rs369938799	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88696709	TAGTATTTGATAAGG[-/T]ATAACAGTATACACA	161436
rs369962329	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711091	GAATCTCACACTTCA[C/T]AACCAGGCAAGTATC	161436
rs369983026	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651130	AAAATGAAATCACAT[C/T]GATGACTTCTGCCTT	161436
rs369997050	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88748814	TCCAAAGGATTAACA[A/G]CAGCTCAGACAATGA	161436
rs370002104	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88700771	GAAAGTGCCTGTACC[A/G]GAAAGGTTAGATCGT	161436
rs370002873	snp	A/C			upstream-variant-2KB	EML5	GRCh38.p7	14:88794333	CTGCAAGCAGTTTAC[A/C]TGCAGGAAATAAAGG	161436
rs370088178	snp	A/C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88702903	GGGACTACTGCTGTG[A/C/T]GCCACCATGCCTGGC	161436
rs370140314	snp	A/C	0.000167986	0.00916323	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627794	CTTGTTCATTGCATC[A/C]CAGATGTGAATAGAA	161436
rs370143623	snp	C/T	0.000167986	0.00916323	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618262	TAATTCTGTCAATAG[C/T]GGCATGATCCATAAG	161436
rs370147913	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619786	TCTCCTGTTTCAGCC[C/T]CCTGAGTAGCTGGGA	161436
rs370156587	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88648351	ACAAGATTCCCAGAA[G/T]AATAATTATTATATT	161436
rs370157734	snp	A/C	0.000463937	0.0152234	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88736369	ATTTGCTTACCTGAC[A/C]GAACGATCATCACTT	161436
rs370177928	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88629509	TTTTCAGGACCTCTC[A/G]AAGTTACTAAAGATG	161436
rs370179059	snp	C/T	0.000266078	0.0115312	intron-variant	EML5	GRCh38.p7	14:88705471	AAAAACCATGTGATA[C/T]GGAAAATTACCTGTC	161436
rs370179425	snp	C/T	3.32094e-05	0.00407475	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622665	TCAAGCCTGAAGGCA[C/T]GGCACCGCCTCAGTT	161436
rs370186656	snp	A/C/T	9.1883e-05	0.00677748	intron-variant	EML5	GRCh38.p7	14:88620739	CTAGAAACTCTATTC[A/C/T]ATTTGTTCACTAACC	161436
rs370216270	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88652873	ATTAAAAAGTGATCT[C/T]TAAATTACTTTGGGC	161436
rs370225715	snp	C/T	0.000171985	0.00927162	intron-variant	EML5	GRCh38.p7	14:88657350	CAATATCTTTTTCTT[C/T]ATCTAATACTAAACT	161436
rs370230416	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88656441	ATGGACACAGGGAGG[A/G]GAATATCACACACTG	161436
rs370246106	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88699085	TTAAAGTACACTTAG[G/T]GCATCTCACTCAGGG	161436
rs370250872	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88755829	AACCATTGTCTCTAC[-/A]AAAAAAAAAATTTTT	161436
rs370270774	snp	C/T	0.000169986	0.00921759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687249	ATGCAGCTCTTTTTA[C/T]AGCATAGGTCTTGAG	161436
rs370272922	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88745698	TCTGCATATGTCAAA[C/T]CCATCAAACTTCACA	161436
rs370277808	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766613	AGCAATTTTAATTTC[A/G]CCCCAGTCCTGTGAT	161436
rs370299888	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88772217	TGGCTCTATCATCAC[C/T]GTCATTTCTGCTACA	161436
rs370330749	snp	A/G	0.00027448	0.0117117	intron-variant	EML5	GRCh38.p7	14:88743991	AGCAGAGAACTAAAC[A/G]TGACTATTATAAAAC	161436
rs370339615	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642864	AGTTAAAAAAATTGA[C/T]AGAGGGATGGAGAAT	161436
rs370359100	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88789076	TCTCAGTTTAAAAAA[A/C]AAAAAAAGCTATCGC	161436
rs370362287	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88712978	CGGTCAGTCTTCATT[A/C]CATATAGACTGTTAA	161436
rs370367101	snp	A/G	7.06639e-05	0.00594365	intron-variant	EML5	GRCh38.p7	14:88638932	AGAATTTGAGAATTA[A/G]GTTTGAAAATTTTAA	161436
rs370371085	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88689630	TCCCAGCCACTTGAG[A/G]GGCTGAGGCAGGAGG	161436
rs370401304	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710659	GTATTCTGTCTTTCC[C/T]ACTTACCTAGCTACA	161436
rs370413914	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88656696	TTCTAGACTAAGACC[A/G]ATAATTCCCATTAAA	161436
rs370416922	in-del	-/ATAG			intron-variant	EML5	GRCh38.p7	14:88661505	CAATACTTAAAAGCT[-/ATAG]ATATGAAACATAATT	161436
rs370417861	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88664275	GAGTGAGACCTGTCT[A/C]AAAAAAAAAAAAAAA	161436
rs370440387	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88728729	GTGTTGTTCAAGGAA[C/T]AACTGTATTTTGGAG	161436
rs370442014	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88755558	TACATCAGCAGAAGG[C/T]GGGGAAAATATAAAT	161436
rs370442538	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88642808	TCAATTACTATTTAT[A/G]GCTTTAACAAAGATT	161436
rs370444569	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88677228	TATTTAATAAATGAT[C/G]CTGGGAAAACTGGCT	161436
rs370446193	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88701554	AAGGAAGGAGAGAAA[C/G]AGCAAGTAAGGAGAG	161436
rs370450451	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88618498	AAAGCTCTGATAAGT[G/T]GGGGAGGAAAGGGGA	161436
rs370461004	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88734065	CAATTTACATTATAG[G/T]CAAAGAGTTAACATC	161436
rs370461834	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763536	CCAACCAAAAAAAAG[C/G]CCAGGACCAGACAGA	161436
rs370483453	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88630629	CAGACTTAAACCAAT[C/G]AGCACATGGTATTCC	161436
rs370509854	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88638710	TAGATTTTGAACAAT[C/T]GATAAATCAATAAAA	161436
rs370540333	snp	C/G/T			intron-variant	EML5	GRCh38.p7	14:88671920	GTTCTTAGAGACCTA[C/G/T]GAAGAGACAACTTAA	161436
rs370553082	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88647334	GCATGCGCCACTGCA[A/C]TGCAGCCTGGGCGAC	161436
rs370554654	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88623164	AGCATTACAGGTGTG[C/T]ACCACCACACCCAGC	161436
rs370579056	in-del	-/GTG			intron-variant	EML5	GRCh38.p7	14:88711428	CAATCATGGCAGAAG[-/GTG]AAGGGGAAGCAAGGC	161436
rs370644692	snp	C/T	2.09945e-05	0.00323988	intron-variant	EML5	GRCh38.p7	14:88696802	AAATGCTATGTGTTG[C/T]CTCTGCATTTTGTTA	161436
rs370675635	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88638969	ACAGCCAAAAGCACT[A/T]ACCCAGAACAATAAA	161436
rs370698412	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88662761	TGTTATCCAGTCTGG[A/T]CTTGAACTCCTGAGC	161436
rs370705380	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88762847	AAGTTAGAACTCAGG[A/G]TTAAGAAATTCACTC	161436
rs370709635	snp	G/T	5.02795e-05	0.0050137	intron-variant	EML5	GRCh38.p7	14:88746155	TTTCCCTTCCAGTAC[G/T]CATTAGAAATCTCAA	161436
rs370767399	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661183	AGCCTCCAACTCCTG[A/G]GCTCAAGCAATCTTC	161436
rs370808638	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691936	GGAAGTATTTTCACT[A/G]CAAGAATATTTGCTT	161436
rs370809285	snp	C/T	0.000175454	0.00936463	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694315	TTCTTACCTGCTTTA[C/T]GCCAAAATTTCATGT	161436
rs370919746	snp	C/T	3.31565e-05	0.0040715	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642991	CTACAGTCTCTGCCT[C/T]GATAACCAAAAATGA	161436
rs370973684	snp	A/G	0.00413403	0.0452761	intron-variant	EML5	GRCh38.p7	14:88622745	ACCAAGCCAGAGTAA[A/G]TGTTCATTATTGGCT	161436
rs370993837	snp	A/T	0.000116348	0.00762629	intron-variant	EML5	GRCh38.p7	14:88616908	ACAAAAGAAAACTCA[A/T]CATGGCAAGTGCGGG	161436
rs370997285	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88762292	GAGGCAGGTGGATCA[A/C]CTGAGGTCGGGAGTT	161436
rs370999647	snp	C/G	0.000167986	0.00916323	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661728	TTTTGTCACTGGTGA[C/G]GCAAGAAGCAGTTAC	161436
rs371009524	in-del	-/A/T			intron-variant	EML5	GRCh38.p7	14:88662561	TTTTTTTTTTTTTTT[-/A/T]AATACAGGGTCTCAC	161436
rs371010197	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88693800	TTTTCGAGACAAGTT[C/T]TTGCTCTGTTGCCCA	161436
rs371024076	in-del	-/AACC			intron-variant	EML5	GRCh38.p7	14:88620608	TAAGTAGTATACAAA[-/AACC]CAGCCATATTTTAGC	161436
rs371038471	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625422	TTTATTTTTTTGAGA[C/T]GGAGTTTCGCTCTTT	161436
rs371064799	snp	A/G	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88670980	ACAAAGTTGTAAAAC[A/G]TACTTCAGGATATCA	161436
rs371075821	snp	C/G	3.51599e-05	0.0041927	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657426	AGGCTTGATTCCTAA[C/G]ATTGGGCGAATATTT	161436
rs371084054	snp	G/T	0.000500835	0.0158167	intron-variant	EML5	GRCh38.p7	14:88736323	TTATGTTTATCTAAG[G/T]ATACATTCCAGCCTA	161436
rs371084352	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88781790	TCCCCTTCTGCCATA[A/G]TTGTAAGTTTCCTGA	161436
rs371137686	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713305	GCTGAGGTAGGAGAA[C/T]CACCTGAACCTGGGA	161436
rs371149724	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627495	TTTTAAAGTGAAATA[C/T]ACCTACAGTACCACT	161436
rs371158979	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733110	TACACTTCTGTGCTA[C/T]CAAAACTTAAAACAA	161436
rs371162368	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757497	TTAAAAACTTTTATG[C/T]TTCTAAGGACAATCA	161436
rs371170654	in-del	-/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88715577	ATAATTTTCAAACAA[-/T]TTTTTTTTGTAAGGA	161436
rs371183665	snp	C/T	0.000167986	0.00916323	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657458	TTGATAAGGCTCTGA[C/T]GGTGTAACTGATTTC	161436
rs371187064	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88755970	GCAATGAGCTATGAC[G/T]GCACCACTGCATTCC	161436
rs371205956	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88668236	CTCATCTTCTGACTG[A/G]ACAGTGACCGACTGA	161436
rs371209976	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644054	TACAGTGAATATATC[A/G]CACAGGGTCAAAATT	161436
rs371224280	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636585	AGAATGGCGTGAACC[C/T]GGGAGGTGGGGGCTG	161436
rs371231776	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88740998	CGAAGTCCCATCTCT[A/G]CTAAAAATACAAAAA	161436
rs371233709	in-del	-/AAGTA			intron-variant	EML5	GRCh38.p7	14:88655066	ATCTTTGTTGGTTTA[-/AAGTA]GATTCAATGCTATCC	161436
rs371256970	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661973	GTTAAATTATTAGTT[A/G]TCTTGGTTTTGTAAC	161436
rs371258075	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88707906	TAAGCACTCTTAGAC[A/T]TCAGAGAGTCTGAAA	161436
rs371266336	snp	A/G			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618323	CCGTTTATAGCAGCC[A/G]CTAGAGACCTTTTTC	161436
rs371306778	in-del	-/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792187	ACCAGAGAGACAGCT[-/G]CGGATTCCCCTCGGG	161436
rs371312945	snp	A/C	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88657598	CAACAATATGAAATA[A/C]ATTAAGTTGTTATAA	161436
rs371323762	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612226	AGCATTGGCCAAAGG[C/T]ACTGAGGCTGCTTAA	161436
rs371341490	snp	C/T	8.62805e-05	0.00656756	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696859	TACCTGAGAAATCAA[C/T]GGCACTAACACCATA	161436
rs371348420	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641044	ATTCCTAGAAACACA[C/T]AACCTCTCAAGATTG	161436
rs371361438	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88669970	GGCAAAGAAGGTCTG[A/G]AGTGGACCTCCAGCA	161436
rs371362201	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88701610	GAAGAATGGGAGAAA[G/T]AAAAAAGGGAGGAGT	161436
rs371371008	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88691011	CAGGGTCTGCCTCCC[C/T]GGTTTGTGGCTGTAA	161436
rs371390266	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88723953	CCAACTCTAACATAA[A/C]CCCCACTCCTGGTGC	161436
rs371409963	snp	A/G	1.65982e-05	0.00288077	intron-variant	EML5	GRCh38.p7	14:88621326	AAGCAGGACCAATAC[A/G]GTGAATGTAATACAA	161436
rs371417660	snp	A/G	1.73234e-05	0.00294302	intron-variant	EML5	GRCh38.p7	14:88740586	AACTAAAAGGTATAT[A/G]GTATAATCAAATTAC	161436
rs371530099	snp	C/T	9.31164e-05	0.00682272	intron-variant	EML5	GRCh38.p7	14:88657519	TACAATAAAAATATA[C/T]GAGTAATTCTTTAAG	161436
rs371542346	snp	C/T	3.34308e-05	0.00408831	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618306	GGCACTTCATAGACA[C/T]GCCGTTTATAGCAGC	161436
rs371566001	snp	C/T	0.000168526	0.00917794	intron-variant	EML5	GRCh38.p7	14:88664490	AGTTATTTAAAGTCT[C/T]ACCTCTAATATCCCA	161436
rs371578525	snp	A/G	0.000153627	0.00876298	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702461	CTGGCCTGTTGCCAC[A/G]TAGTCTTTCAAAGGA	161436
rs371583252	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88702028	ACTTTGGTAAACCTG[A/C]ATAGATTACTATCAT	161436
rs371586642	snp	G/T	0.000167986	0.00916322	intron-variant	EML5	GRCh38.p7	14:88644402	AACTCTGGATACATT[G/T]CAGTAACACTGGAGA	161436
rs371608676	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88793036	CCCCTCCCGGAGCCG[A/T]GAAGAGGCTGGAGTT	161436
rs371629487	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680604	ACATACATTAACTGT[A/T]CTCATTATAGTACTA	161436
rs371652133	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731518	ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG	161436
rs371683177	snp	C/G	0.0115144	0.0749975	intron-variant	EML5	GRCh38.p7	14:88773776	CAGGAATCTGGAGCA[C/G]TGTTCTCAAACTTTA	161436
rs371745317	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88690602	GCAAATTGAAAGTAG[C/G]AACAACTGTTTAGAG	161436
rs371746081	snp	G/T	1.66324e-05	0.00288374	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714957	GCATTCTATAAAAAA[G/T]TCTTTTCCCATTTCC	161436
rs371746463	snp	G/T	0.000102928	0.00717311	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88754578	CTTTAAAACTGATAT[G/T]GTCTGCACAGTGTAT	161436
rs371792609	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88728429	ACTGGAAGTCTTATC[A/G]ATAACACAAACAGTT	161436
rs371827996	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748022	AAGTCCTGTAATCAC[C/T]CGAGCTTCCATCTAG	161436
rs371831548	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88686578	TAATTTCAGTGCTTC[G/T]GGAGGCCAAGTTTAG	161436
rs371835017	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88769129	AATTTTGTAGTGGGT[A/G]AGGGCATTGATATAG	161436
rs371837079	snp	A/G	0.000163987	0.00905354	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688349	GATGTCTCTCCAGAT[A/G]CACACATCTCCTGTG	161436
rs371859882	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88691609	CCCTTAGGGGAGAGA[C/T]TAATAAATCATAACT	161436
rs371868165	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88747551	AAAAAACATCAGATA[G/T]GGCATTATTAGTTAA	161436
rs371875020	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88790016	ATTACATCTTCTGCT[A/G]TGGCATAATTTAAAA	161436
rs371875356	snp	C/T	1.66974e-05	0.00288936	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88622707	AGTTTAACCGCTCCT[C/T]CTTCTTTTGACCTAA	161436
rs371882127	snp	A/T	7.93871e-05	0.00629978	intron-variant	EML5	GRCh38.p7	14:88738867	GTAATAAGACATTTG[A/T]TTTGTTATTACCTTT	161436
rs371888369	snp	A/G	0.000174675	0.00934381	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702596	TTCACCAATTTGAGT[A/G]TAAAACAGATTACTT	161436
rs371921424	snp	C/T	1.66651e-05	0.00288657	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712379	TTATATCGTTGATAT[C/T]TGAATACTTGGGCCA	161436
rs371943483	snp	A/C	0.000562942	0.0167676	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736471	AATTAGAAAAGGTTT[A/C]TTTCTTTCTTGCACC	161436
rs371948981	snp	A/G	0.000251503	0.0112111	intron-variant	EML5	GRCh38.p7	14:88644422	AACACTGGAGAGTGA[A/G]TTTTCCTTACCTCTA	161436
rs371950638	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88623119	CTCCCAGGTTCAAGC[A/G]ATTCTCCTACCTCAG	161436
rs371954725	snp	A/C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629909	TCTTAGTTTCCAGTA[A/C/T]AGAGATGCCATAAGT	161436
rs372030509	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88656701	GACTAAGACCAATAA[C/T]TCCCATTAAAGACAA	161436
rs372033391	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88719375	TGGGCAACAGAGCGA[A/G]ACCTTGTCTCAATCA	161436
rs372057843	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764435	TATTCTCCTTTTAAC[A/G]TCTTTAGGTCAATAG	161436
rs372059291	snp	C/T	0.000167986	0.00916324	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665409	CCTCTAGAGTATCCG[C/T]ATTTGCCATTAAGAA	161436
rs372070923	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88740027	GGCAATTAAATTTTC[A/G]TGTAAATAACTTACT	161436
rs372082809	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88708799	TTATATGCTCACAAG[G/T]TACCTTTTGATTATG	161436
rs372107522	snp	C/T	1.68269e-05	0.00290055	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715066	AACTTTTTTATAACG[C/T]TGAGCAACTCCATAA	161436
rs372152722	snp	C/T	1.658e-05	0.00287919	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658239	ATCACAAGGCCTTTT[C/T]TCTCGATAGCCTTCC	161436
rs372162801	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88742769	GTATTAAATATTTGT[A/C]AAAAAATAAATATTT	161436
rs372171487	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613621	AAACATTTGTTGGAT[A/G]ACGTGGTTTAAAATG	161436
rs372175904	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88735758	AAATACACAAAACTG[C/G]AGGAAACTAATCTTC	161436
rs372184561	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639672	ACCTCCACTTCCCTG[A/G]TTCAAGCAATTCTCA	161436
rs372186264	snp	A/G	0.000256955	0.0113319	intron-variant	EML5	GRCh38.p7	14:88618643	GTATACAGTATTGGT[A/G]CTGTACCTGGAGATA	161436
rs372267347	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742106	AATGGGATGCCTGGA[C/T]TCCCAATTGAGATGA	161436
rs372282087	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778986	TGAAACTTCCATGCT[A/C]AAGCATTTAGATTGT	161436
rs372297965	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674410	GGCAAAGGAGAAGCA[A/G]GCACCTTCTTCACAG	161436
rs372332334	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88637554	ATTCTATTTGCAGAA[C/T]GTAAATCCCATTAAT	161436
rs372354235	snp	A/G	6.24083e-05	0.00558572	intron-variant	EML5	GRCh38.p7	14:88739042	ATAAAATAATTTAAC[A/G]ACAAATATTTTTTAA	161436
rs372370268	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679198	ACTGATTATATCTGC[G/T]AATACTCTATTTCTA	161436
rs372383945	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652080	GTCCTTTGCACTATA[C/T]GATGCTGCATTCTAG	161436
rs372384304	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88691937	GAAGTATTTTCACTG[A/C]AAGAATATTTGCTTT	161436
rs372389467	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631510	ACGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT	161436
rs372421058	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705077	ATTGTCTGAAAACAA[C/T]AGCTTTAATAGTAGT	161436
rs372445976	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687460	AAAGAACAGGAATTA[A/G]CTTAAGAATCCATTG	161436
rs372447776	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88646138	TAACCTTCCCATATA[A/G]AAGACTCCAACATTT	161436
rs372474548	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88784625	ACCAATAACAAATAA[C/G]AAGATCAAAGCCATA	161436
rs372567577	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88624427	TGACAAATCAAATCA[C/T]AAGTATCTGGTTACT	161436
rs372575534	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88718916	GCCAGGAGACAACTT[C/T]TGGAACTTACTACTC	161436
rs372615702	snp	C/T	9.95256e-05	0.00705357	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625050	CCCGTTGTGAGCTCT[C/T]GCCACGATTCTACAC	161436
rs372617526	snp	C/T	5.34288e-05	0.00516832	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695407	AGTCCCAGAGCACAA[C/T]AGTATGGCTATCATC	161436
rs372620794	snp	G/T	0.000169986	0.00921759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638841	ACTATGTTGATAAAT[G/T]TGGGGTGCTGGTTTA	161436
rs372630387	snp	C/G	3.36293e-05	0.00410043	intron-variant	EML5	GRCh38.p7	14:88746327	GAATAAAAAGGCAAA[C/G]AAATCAAAGAGAAAC	161436
rs372630404	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88686277	GAGAGAGTGTGGTGC[C/T]ATGCCTTAAAGGAAG	161436
rs372658522	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88730456	AATCATTTTGAATTG[-/C]AGCAGCTTAAGAAAT	161436
rs372665750	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88683367	AGCCTGTGGCACAAT[A/T]TATACCCAAGGAAAA	161436
rs372676042	snp	A/G	3.33483e-05	0.00408327	intron-variant	EML5	GRCh38.p7	14:88658399	TTCCCCTAAAGAGGA[A/G]GAAAATTCAAACAAT	161436
rs372677784	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88639446	TCAGCCCACGATCCT[C/T]CTGTTTTGGTTTCTC	161436
rs372680115	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88737469	TGCCAGGCCAAGTGG[G/T]CAGGGTACCTCCTGG	161436
rs372797411	in-del	-/TTTTTTTTTTTTTT			intron-variant	EML5	GRCh38.p7	14:88727056	TTGTTGTTGTTGTTG[-/TTTTTTTTTTTTTT]TTGTTGTTTTGGTAT	161436
rs372832091	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88781549	ATTTCTTATTGATAT[C/G]GTTTAGTTGTGTCCC	161436
rs372843421	snp	C/T	0.000250115	0.0111801	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705489	AAAATTACCTGTCGA[C/T]GGTAGGTGAGCTGTG	161436
rs372849559	snp	A/G	6.63262e-05	0.00575836	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665458	TACGGCTAAAGCTTT[A/G]CCATCAGGAGAAAAA	161436
rs372903362	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88711961	AAAAAAAAAAAAATA[C/G]AACCATCATTGTACA	161436
rs372919299	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626931	AGCTCTTCCTGCCAG[A/G]GTCCAGAACTTCACA	161436
rs372925477	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676068	TTCCAAACTTTCTTA[C/T]ATTTTCCTATCTGCT	161436
rs372933962	snp	A/G	6.44102e-05	0.00567459	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726582	ATCCTTCATTCCAAG[A/G]GCAAGATGGATTCCA	161436
rs372946905	in-del	-/ACAAA			intron-variant	EML5	GRCh38.p7	14:88778801	ACAAAACAAAACAAA[-/ACAAA]GTGGTAAGTTAAATA	161436
rs372950228	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88656750	TTTTGAAATGAGGAC[G/T]GACTATGCTTAAAGA	161436
rs372952433	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88646193	GGCATAAAATATACT[C/T]GCATTTTCAAAATGG	161436
rs372961727	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88730580	TTAATTTAAAAACAC[G/T]ACAAATAATTTTGAG	161436
rs372989084	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88676851	CTATGTCCATTTGAT[A/C]TTTGACAAACCTGAC	161436
rs372989316	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651944	ATAAGTTAGGGATTA[C/T]AATGTTCATTTTGCC	161436
rs373016992	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88701415	ATCACAACTCAGAAT[G/T]TGAGTTTTCACCATG	161436
rs373029913	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88743200	GAATAAGTTCTACTA[C/G]TCTATACCACTGTAG	161436
rs373038075	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765705	TATGGATATCTTTGG[A/G]GCCAGTCTGGCTACC	161436
rs373043518	snp	C/T	0.0126979	0.078662	intron-variant	EML5	GRCh38.p7	14:88720493	ATGCAAATCAATAAA[C/T]GTAATTCATCACATA	161436
rs373043769	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88775133	GTACTATGTCAAGGG[C/G]CTTAAGTGAGCCTCT	161436
rs373047856	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88771010	CTTTAAGTATTTAAT[A/C]TCTAAATTTATCATA	161436
rs373049178	snp	C/T	0.0115144	0.0749975	intron-variant	EML5	GRCh38.p7	14:88733147	AGGTCTCCACTGCCA[C/T]ACAAATCTGCAGCAG	161436
rs373080367	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88736029	TTTTTTGAGATGGAG[C/T]CTCACTCTGTTGCCA	161436
rs373106453	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612030	CATGTTTGTGCACTG[C/T]TGTTGTGAGGATCAG	161436
rs373124974	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660714	TGCCACTGCACTCCA[A/G]CCTGGCGACAGAGTG	161436
rs373140887	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88761276	TTGCATAGGTATACA[A/T]GTGTCATGGTGGTTT	161436
rs373144086	snp	A/G	4.98716e-05	0.00499333	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616153	TAACCTGCAGTCATC[A/G]CCTCCAGCACTAACA	161436
rs373155953	snp	C/G	6.37694e-05	0.00564629	intron-variant	EML5	GRCh38.p7	14:88715222	AAAAAAATGAGACTA[C/G]ATGAACAGAAGTCAC	161436
rs373189120	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786755	ATTTTCTCGTGCTGC[C/T]GCCATGTAAGAACTG	161436
rs373203934	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88714832	GAAATATTAGCTCAG[A/C]TCTTCTTTGATTTCC	161436
rs373215664	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744929	ATACATATTACAGTT[A/G]ATATTTAACAACTCA	161436
rs373235570	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88726048	TTGAATTTATCTATC[C/T]ATAATTCAACACAAA	161436
rs373252219	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88635460	CTGGAGAGACTAGGT[C/T]TGTCTCTGAATATTA	161436
rs373257908	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88704700	TTGTCTAATGTCTCC[G/T]CATGATTAGATTCAG	161436
rs373267038	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88732208	TTTTAGGTCTAACAT[G/T]TAAGTCTTTAATCCA	161436
rs373274800	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88682456	GAAAATAGTTCCAAG[C/G]AGATGCAACAAAGGA	161436
rs373275803	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88709072	TAATATGATCTAAAT[A/G]TTTTCAATATATGGT	161436
rs373281975	snp	A/G	1.66391e-05	0.00288431	intron-variant	EML5	GRCh38.p7	14:88644516	TCACTGGAGGCCTGC[A/G]ACAGAGAAGTGGGGA	161436
rs373293272	snp	A/G	0.000108459	0.00736326	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615811	TCTGTAGTCATCTCA[A/G]CATCTCTCAGTGAGG	161436
rs373303659	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88667598	TCAGTTCCAAATCTG[A/C]CACTTTGGGCCTCAC	161436
rs373317962	snp	A/G	8.42424e-05	0.00648954	intron-variant	EML5	GRCh38.p7	14:88657351	AATATCTTTTTCTTC[A/G]TCTAATACTAAACTA	161436
rs373319978	snp	A/G	1.65737e-05	0.00287864	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740510	CAGTATTGTCTGAAG[A/G]TCACCCGTCTTACCA	161436
rs373383288	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675537	CCTGGCCCACAAAAC[C/T]ATCTTTTCCTCCTAG	161436
rs373395296	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88629808	GTATGCTGTTCTCAG[C/T]ATCCAGGTTCCACTC	161436
rs373400628	snp	C/T	0.000130563	0.00807863	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694366	AGTTTATCAGGCACA[C/T]AGGGGTTCATCTTTA	161436
rs373401925	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88618011	AAACTTTGATTTCCT[A/T]AAAAAAAAAACTTGA	161436
rs373412253	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88640996	CTAAAAAAAGAAGAA[G/T]AAGAAGAAGAAAAAT	161436
rs373417908	in-del	-/CA			intron-variant	EML5	GRCh38.p7	14:88756850	AAATAAATGGAAAGA[-/CA]TCTCATTTCTGGGCT	161436
rs373447581	in-del	-/AATCA			intron-variant	EML5	GRCh38.p7	14:88763287	AAGAAAAGAGAGAAG[-/AATCA]AATAGACACAATAAA	161436
rs373456182	in-del	-/GAGAGA			intron-variant	EML5	GRCh38.p7	14:88775919	GAAGAGAGAGAGAGA[-/GAGAGA]CTCCATTTGTTTGGG	161436
rs373473773	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641205	AGCTGGTGCCAATCC[C/T]ACTGAAACTATTCTA	161436
rs373476855	snp	A/C	0.00072937	0.0190828	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665451	TGAGACCTACGGCTA[A/C]AGCTTTACCATCAGG	161436
rs373488375	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88769377	TCTGCCATGACTGGA[A/G]GCTTCCTGAGCCTCC	161436
rs373503555	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88689659	GGCTAGCTTGAGCCT[A/G]AGAGGCAGAGGTTGC	161436
rs373506671	snp	C/T	3.41012e-05	0.0041291	intron-variant	EML5	GRCh38.p7	14:88646999	AGATTACAACATAAA[C/T]TTGAATTGAAAACAC	161436
rs373510031	snp	A/G	4.98451e-05	0.004992	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621141	TCCCAAAGTCTCACT[A/G]TCCCATCTTCTGCAG	161436
rs373512419	snp	C/T	0.0003161	0.0125678	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704944	TGTTTCTCTTTGCAC[C/T]GTTCTTTAAGCTGAG	161436
rs373515401	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88693350	CAATCATGGCTGAAG[A/G]TGAATGAGGAGCAAA	161436
rs373538008	snp	A/G	0.000215523	0.0103786	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88681969	TTTATCATCGCTTAC[A/G]GTAGCACAGATGGGC	161436
rs373625701	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88638978	AGCACTTACCCAGAA[A/C]AATAAACTACTCTTT	161436
rs373716726	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88763903	TATAGCCGGGTTAAA[G/T]AAGTGGACTTCTAGT	161436
rs373722440	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88746292	CCAAGCGCTGATTTA[C/T]GTCCAAGAAGTCCAG	161436
rs373760000	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671414	AGGAAGCACTAAATA[C/T]GGAAAGGAAAAAGTG	161436
rs373799820	in-del	-/CAACAA			intron-variant	EML5	GRCh38.p7	14:88733971	AAATAACAACAACAA[-/CAACAA]GAATTTTTGCTTACC	161436
rs373813729	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652631	CAAATTGTCCACTAA[C/T]TTCTCATAATAAAGT	161436
rs373832059	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88751556	GTTCGAATAAAGAGA[G/T]AATTCAGTTTTAAAT	161436
rs373856533	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88753489	TGAATTAAAAAGCAG[A/G]TAACTAAAATTGTTC	161436
rs373857538	snp	A/G	0.000116187	0.00762104	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616255	TGCCTAAAAAACAAT[A/G]ACAGACAAGCTCAGG	161436
rs373882117	snp	A/G	0.000153824	0.00876859	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661699	TCCCAAATCGTCCCC[A/G]GTAGCTAGAACCATT	161436
rs373962256	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88749156	ATTGCTGAAGCCATC[A/G]CTAAAGGGCAAATTC	161436
rs373967813	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700967	CTGGGTTTTTTTTTG[C/T]CCTACTTTTACAGAT	161436
rs373983606	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88705634	TTTAAAGAAGATTCA[C/T]TTTCAAAACAGCACT	161436
rs373987713	snp	C/T	1.66563e-05	0.0028858	synonymous-codon, missense, nc-transcript-variant	EML5	GRCh38.p7	14:88622700	ATCCCACAGTTTAAC[C/T]GCTCCTCCTTCTTTT	161436
rs373988184	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88734845	AATAAACTGTAAGAA[C/G]AACAAAAAGGGAAGG	161436
rs374011094	snp	A/C	5.93525e-05	0.00544727	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88744027	CCTTCTAGTACCTTG[A/C]TATGTTTTACACCAC	161436
rs374016369	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88651154	CTGCCTTGTCATTTT[-/C]TTTTTTTTTTTTTTT	161436
rs374038849	snp	C/G	1.67343e-05	0.00289255	intron-variant	EML5	GRCh38.p7	14:88664664	ACATTTTCTATCTTT[C/G]GAAATACTTTTTTAC	161436
rs374058236	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88623812	TTCTAGTGAGTGGGG[C/G]TGTGCAGGAGTAAAT	161436
rs374060566	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88721998	CATTTATGTGGCCAA[A/C]AAACATATGAAAAAA	161436
rs374090521	snp	A/T	0.00120409	0.0245071	intron-variant	EML5	GRCh38.p7	14:88656617	AACTTAAAGTATAAT[A/T]AAAAAAAAGTGATCT	161436
rs374135273	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88618493	GGAGAAAAGCTCTGA[C/T]AAGTGGGGGAGGAAA	161436
rs374179617	snp	C/T	3.31373e-05	0.00407032	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736373	GCTTACCTGACCGAA[C/T]GATCATCACTTCCAG	161436
rs374191061	snp	C/G/T	3.3268e-05	0.00407837	synonymous-codon, missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746187	AGAGAATACTTACTC[C/G/T]ATCTGTATGACCAGG	161436
rs374192897	in-del	-/ATTT			intron-variant	EML5	GRCh38.p7	14:88676903	ATTTCCTATTTATTT[-/ATTT]GTTTGTTTGTATTTT	161436
rs374230213	snp	A/G	0.000281674	0.0118641	intron-variant	EML5	GRCh38.p7	14:88621304	CAAGGATCTTGCCCT[A/G]AAACACAAGCAGGAC	161436
rs374242904	snp	A/G	8.63968e-05	0.00657198	intron-variant	EML5	GRCh38.p7	14:88740584	AGAACTAAAAGGTAT[A/G]TAGTATAATCAAATT	161436
rs374297855	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633953	TTGAGTTCAGAATCA[C/T]GACATTAAAATAATG	161436
rs374298123	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668378	AGGGAGTCAGTGAAG[C/T]AGAGAGAAGAAACAG	161436
rs374309740	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88632352	CCCTCTACATTCTCA[A/G]TAATATAGTGAGAGT	161436
rs374317627	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706053	TTTGATAGATTAAAA[C/T]GCAATCAAAATTACT	161436
rs374364038	in-del	-/A	0.5	0	intron-variant	EML5	GRCh38.p7	14:88660298	AAAAAAAAAAAAAAA[-/A]GAAAGGAATGCATTG	161436
rs374371445	in-del	-/AGA			intron-variant	EML5	GRCh38.p7	14:88705627	TTACTTGTTTAAAGA[-/AGA]TTCATTTTCAAAACA	161436
rs374374284	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663998	ATTGAAAAGTGTAGG[C/T]TGGGTGCAGTGGCTC	161436
rs374379690	snp	G/T	0.000129237	0.00803751	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657432	GATTCCTAACATTGG[G/T]CGAATATTTGTTGAT	161436
rs374383872	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768702	CAGGCGTGAGACATC[A/G]CACCTGGCCTATAAT	161436
rs374420178	snp	A/G	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88729857	TAAGCCACCACACTC[A/G]GTCTTGTTTTTTGTT	161436
rs374424889	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698442	CGGCTAATTTTTGTA[G/T]TTTTTGTAAAGATGG	161436
rs374436164	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88654956	TTATGAATCTGGGTG[C/T]TCCTGTATTGGGTGC	161436
rs374476714	snp	A/G	8.32674e-05	0.00645188	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618263	AATTCTGTCAATAGC[A/G]GCATGATCCATAAGA	161436
rs374489383	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88723656	TGTTAACTAGCTTGA[G/T]GTAATCATTTCACAA	161436
rs374527067	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630810	CATAACTCCAATTGC[C/T]ACTGCAGCCATTTTC	161436
rs374556083	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88716819	GTATTTTAGTATAAT[A/G]TCGCTCCGTCAATAT	161436
rs374558540	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764130	ATATTATCCTACTGA[C/T]GGATTTTATTTGCTT	161436
rs374580506	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88713410	AAAAAAAAATACTAA[A/T]AGGTAATATTTTGAT	161436
rs374580747	snp	C/G	3.41775e-05	0.00413371	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696938	CCATATATGAATTGA[C/G]GGATCTCTACCAACC	161436
rs374597557	snp	C/T	8.68138e-05	0.00658782	intron-variant	EML5	GRCh38.p7	14:88740588	CTAAAAGGTATATAG[C/T]ATAATCAAATTACCA	161436
rs374598692	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772828	TTTGTTCACTACACT[C/T]CAGCTACACTGGCCT	161436
rs374601119	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88639175	AATGCTATGGGAATT[C/T]AGAGCAGAAAAGATT	161436
rs374602200	snp	C/T	7.36743e-05	0.00606892	intron-variant	EML5	GRCh38.p7	14:88702425	AGCTTATCTGGCTTA[C/T]TGTCAGTCTTTCAAA	161436
rs374603286	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763866	AGGAATAAACTTAGC[C/T]GTAGGTTTTTACAGA	161436
rs374611793	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725354	TGTTAACTTAAAAAC[C/T]GGTCTCGGAAAGGGG	161436
rs374659075	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88791266	ATTTGAAATGCCCAA[C/T]TTAAATCCTGTGCAA	161436
rs374668618	snp	A/C	1.66546e-05	0.00288566	intron-variant	EML5	GRCh38.p7	14:88621340	CAGTGAATGTAATAC[A/C]ACAGCTGCTTTTCTT	161436
rs374691227	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88758918	ATATAAGGGCCACAT[A/G]TCATATTAATACATT	161436
rs374705269	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88661230	AGTAGCTAGGACTAC[A/C]GGCATGTGCCACAAT	161436
rs374714875	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691033	TGGCTGTAACTAGCA[C/T]CTGCCCAGAGTCTGG	161436
rs374722194	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88644802	TGCAACCTCTGCCTC[C/G]TGGATTCAAGCGATT	161436
rs374722396	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88662964	ACTAAACGATAGAAA[A/G]TAGGTATCAGTTTTC	161436
rs374725035	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88699139	GGGAGAGTTCTCAGA[C/T]AGGCTTAGCCTAAGT	161436
rs374738032	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687424	CTAGAAAAAAGAACA[C/T]AGTCAAAAGTTACAG	161436
rs374740277	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768404	TACTAAAATATTTCC[A/G]TAATGTGATTGTCTT	161436
rs374748801	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88789187	TATTTTATAACTTAG[G/T]CTTAAATCTAGACTA	161436
rs374765877	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88630934	ATGAAACTCCTGAAG[G/T]AGCACACTCCGGAGG	161436
rs374802581	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88781384	CTCAAATGTAATAGA[C/T]TTATAAATCAGAATG	161436
rs374821017	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88719852	ATTAATCTAGGATCT[A/G]GTTTTTTGAAAAAAT	161436
rs374841375	in-del	-/AAAAG			intron-variant	EML5	GRCh38.p7	14:88664310	AGAAAAAGGAAAAAG[-/AAAAG]TCTCAACTCTATAGT	161436
rs374841988	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701774	CTGATTGATCTTAAG[C/T]AAATTATTTAATTTC	161436
rs374851347	snp	C/T	0.000165986	0.00910855	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88681939	ACTAGGTGAGAGATC[C/T]CATATTCTTAAGGTT	161436
rs374873882	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88729866	ACACTCGGTCTTGTT[C/T]TTTGTTTTTTTTTTT	161436
rs374926294	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675407	TGCCAAGGCTTGAGG[C/T]TTCTGATCTGAAGCA	161436
rs374928402	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633044	CTAAAGCCTTAAGTA[C/T]CTCTGAGTCCTGTGA	161436
rs374973838	in-del	-/CACT			intron-variant	EML5	GRCh38.p7	14:88645792	CTCTTCCCTTATTCT[-/CACT]ATTTACTAAAAATGT	161436
rs374987142	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766439	TCTGTCTTTTACAGT[C/T]GTGGATAAGGGATGA	161436
rs374998548	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765680	AATTCACAGGTTCCA[A/G]GAATTAGAGTATGGA	161436
rs375028510	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692102	AGGATGGGCTGGGCA[C/T]GGTGGCTCATGTCTG	161436
rs375039945	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642517	TCACCCAACATGCTA[C/T]ATTCAATCACTATCA	161436
rs375050237	snp	A/G	1.74461e-05	0.00295343	intron-variant	EML5	GRCh38.p7	14:88622764	TCATTATTGGCTACT[A/G]TAATTTTTATTATAA	161436
rs375105242	snp	C/T	6.63185e-05	0.00575802	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658243	CAAGGCCTTTTTTCT[C/T]GATAGCCTTCCATCT	161436
rs375119683	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88732303	AGCCAGTTTTCCCAG[A/C]ACCATTTATTAAATA	161436
rs375126885	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88739528	TGTAAAAATGAATTA[C/T]ACATGAACTTAAAAA	161436
rs375167655	snp	G/T	0.0178098	0.0926698	intron-variant	EML5	GRCh38.p7	14:88706796	ACCCAAGCAGCCAGA[G/T]GATCCTTTTAAGACT	161436
rs375173864	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88711384	GTGTTCAGCAGTTCA[C/G]CATGGCTGGGGAGGC	161436
rs375181358	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88784147	TGGGATACTGCAAAA[C/G]CAATACTCAAAGGGA	161436
rs375235878	snp	A/G	0.0126979	0.078662	intron-variant	EML5	GRCh38.p7	14:88664328	AGTCTCAACTCTATA[A/G]TATTCATCTTCAGAT	161436
rs375251901	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88674345	GATTTAATTGACTCA[C/T]AGTTCTGTATTTCTG	161436
rs375262590	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88621013	TCCCCTCAAAATGCT[A/C]AACAGAATTCTGGCA	161436
rs375270780	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640480	GAAATTAAGGCAAAA[A/C]TTTAAAAAAAATCTT	161436
rs375302297	in-del	-/GT			intron-variant	EML5	GRCh38.p7	14:88771349	TTCACTAATCTAACT[-/GT]ACTGGCAGACTCTGA	161436
rs375321617	in-del	-/AAA			intron-variant	EML5	GRCh38.p7	14:88647687	GAGTGAGACCGTCTC[-/AAA]AAAAAAAAAAAAAAA	161436
rs375326119	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88724061	AGATCACAGGGTCAG[A/G]AGATCAAGACCATCC	161436
rs375331672	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673800	GAAGAGAATAAAATA[C/T]CTAGGAATATAGTTA	161436
rs375342505	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758402	GTTTCACCATGTTGA[C/T]CAGGATGGTCTCAAA	161436
rs375344426	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88779692	ATTCTAGGCGCAAAC[C/G]AGGATCAGCTGTTTC	161436
rs375348724	snp	C/T	0.000165986	0.00910854	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665426	TTTGCCATTAAGAAG[C/T]TTCCATCGTTGAGAC	161436
rs375350956	snp	A/C	0.0146672	0.084371	intron-variant	EML5	GRCh38.p7	14:88747111	TCAAAATAAGCTAAA[A/C]AAACAAACAAAAAAA	161436
rs375366195	snp	C/T	0.000110044	0.00741688	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738947	GTTAAATCCCAAAGA[C/T]GAATACAACCATCTC	161436
rs375371587	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88662286	GGCCAAGATAAAAAA[A/T]AAAAAAAAAAAGGCT	161436
rs375374450	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646880	AACAGTATCCCATTA[A/G]TGCTAAATATGGAAG	161436
rs375379895	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88737030	GGGTACCCTCTCCAT[C/T]GAGAGCTGTTTTGTC	161436
rs375408162	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88657871	TACATTTTCTATAAC[A/G]AGCTGATATTACTGG	161436
rs375417162	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768536	CTGCCTCAGCCTCCT[A/G]AGTAGCTGGAATTAC	161436
rs375425132	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88726941	TGGCGTGATCATAGC[C/T]TACTATAACCTTGAC	161436
rs375425802	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88681761	GGCACCATGAGCAAG[C/T]AGACATTGAATAAAT	161436
rs375445382	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88619610	TTGTCTTAATATTAA[A/G]CAAAGAACACAGCCC	161436
rs375453720	snp	A/C/T	2.14085e-05	0.00327166	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615815	TAGTCATCTCAGCAT[A/C/T]TCTCAGTGAGGTGTA	161436
rs375480972	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88769151	TTGATATAGTTGGAT[C/G]TGTGTCCCCAACCAA	161436
rs375506792	snp	C/T	1.6593e-05	0.00288031	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88643011	ACCAAAAATGAGCTC[C/T]AACACAAGGTCCTAT	161436
rs375543692	snp	A/G	0.000139179	0.00834087	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715091	CCATAAATATCAACC[A/G]AGCTGTCATTGCATC	161436
rs375544483	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88668508	AACCAGGAAGTGATC[A/G]ACAGATTGGCAGCAG	161436
rs375551528	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88794449	AGCTTTCTGGCAGCT[A/G]CTGCAAATAAACAAA	161436
rs375635234	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88655935	CCATCTCACATCAGT[C/T]AGAATGGTGATCATT	161436
rs375635459	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752877	GCCCAGGATGGTCAG[A/G]AGAAGATTATCTTCC	161436
rs375646142	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88772933	GCATTCATATTATTC[A/G]TGCTTTGGGGCAAAT	161436
rs375658073	snp	G/T			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614736	GTGAAAAGAAATAAG[G/T]ATCTAAGAATTCAGC	161436
rs375714564	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88721262	AGAATTAGAAAAAAA[-/A]CTACTTAAGACATCA	161436
rs375724094	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88793218	CTGCCGGTTCCGCAC[A/G]GTCCCTGCACCCAGC	161436
rs375726213	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772120	CACCATCCATTCAAT[C/T]GCTCAGACCAAGAAG	161436
rs375727661	snp	A/G	0.000132786	0.0081471	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695443	CAACTGATGCCAAAC[A/G]TTTCCCATCCGCTGT	161436
rs375729601	snp	C/T	5.21145e-05	0.00510437	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638907	TAAAAACTCTGAGAA[C/T]CTACAAAAAAGAATT	161436
rs375765728	snp	C/T	3.72641e-05	0.00431632	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620854	TTTTCATTCCAATAG[C/T]CACCATGTCCCCTTC	161436
rs375791433	snp	C/G	2.47871e-05	0.00352036	intron-variant	EML5	GRCh38.p7	14:88620724	TAAATCAAGTATATA[C/G]TAGAAACTCTATTCC	161436
rs375803002	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88715958	GATATTAGTAACAAC[A/C]AAAAGATGGATAAAT	161436
rs375804488	snp	A/G	0.00013403	0.00818518	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88704862	AGTTGTTTTATACCC[A/G]TGAACAAAGTGTAAT	161436
rs375850507	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88636856	TAACTAAGCTTCCCA[A/G]GGAAACGTTTACTTC	161436
rs375879247	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88731989	CAGATGAGTAGAGTG[C/T]AAAAATTTTCTCCCA	161436
rs375898362	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762276	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	161436
rs375919440	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88642783	TATTCTGGAGTGTTT[C/T]TCCTACATTTCAATT	161436
rs375932150	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88680637	TTTCAAATTTTTATG[C/T]TAATTTTAGGTTCCA	161436
rs375972882	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88775469	AGGGAACATTGGCAG[C/T]AGTCTGGTAGTGCTC	161436
rs375979945	snp	C/G	1.68937e-05	0.0029063	splice-donor-variant	EML5	GRCh38.p7	14:88754511	AAAAACTGTCACATA[C/G]CTGTCCATCTAAGTC	161436
rs376019721	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88731311	ACCTATGAGTGAGAA[C/T]ATGCAGTGTTTGGTT	161436
rs376028787	snp	G/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765426	CAACTGCATGCCTCA[G/T]GATGTTACCACCTCC	161436
rs376042112	snp	C/G	0.000291471	0.0120686	intron-variant	EML5	GRCh38.p7	14:88687200	TATACAAAAACCCCA[C/G]TAAGTCTCAAATCAC	161436
rs376073448	snp	A/G	5.01928e-05	0.00500938	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618239	TTACCTAGTCCATGT[A/G]GCCCAAGTAATTCTG	161436
rs376074219	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612576	ACAAGATTATAAATG[C/T]ACATATATATTCTCA	161436
rs376075359	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88729250	ATAGCTGAACAGAAT[C/G]GTGAAAATAGCATAA	161436
rs376085514	snp	A/G	0.000167986	0.00916323	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661759	ATCTGTAACTTCTCC[A/G]ATTACTGGCCAAATT	161436
rs376088108	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88676894	TGGGGAGAGGATTTC[A/C]TATTTATTTGTTTGT	161436
rs376089213	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88701499	GAATGTGCTTGATGA[A/G]TGTTTTTGAGTGAAT	161436
rs376094970	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88643400	CAATAAAAAATAACA[C/T]TTAAAACACAATATT	161436
rs376097064	snp	A/C	3.33489e-05	0.0040833	intron-variant	EML5	GRCh38.p7	14:88736335	AAGGATACATTCCAG[A/C]CTATGGAATTAGTTT	161436
rs376106778	in-del	-/TAAAG			intron-variant	EML5	GRCh38.p7	14:88756435	AGCAATCCCACTAAG[-/TAAAG]GGAAAAAACAAGGAT	161436
rs376123912	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88713106	AAATAAAGTACTATG[C/T]AGTGGCTGGGTGCAG	161436
rs376142163	snp	C/T	4.58831e-05	0.00478952	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657488	CATTCTCCCTTGTAA[C/T]ATCACTGTCATAGCC	161436
rs376147247	snp	A/T	0.000169986	0.00921759	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712332	ATCAGCTGTAACTAA[A/T]ACTTGGCCAATATAA	161436
rs376156000	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783565	AGTAAAAAAACAAGT[A/G]ACAAAGTCACCGTAT	161436
rs376180674	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88631291	TGATCATGACACACC[G/T]CAGCCTCGAATTCCT	161436
rs376180752	in-del	-/AGTT			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613407	ATCATTTATAAAGAT[-/AGTT]TTGTTCTCAGTTTCA	161436
rs376182375	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88774367	CTGCTGGAACAAATC[C/T]GTTTTTAAGAAATGT	161436
rs376207771	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88659683	ACCATCTGGAACGCT[A/G]GAAGTGAAGTTTCTG	161436
rs376221071	snp	A/G			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616362	GGAGTTAGCACCGCA[A/G]CCAGTGATTAGAATG	161436
rs376263535	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790501	GCTAGAAGAACAAGA[C/T]GTAATTTACCTCACC	161436
rs376266218	snp	C/T	0.000313725	0.0125206	intron-variant	EML5	GRCh38.p7	14:88702678	ATTTTGGCCTTTTAT[C/T]TGATCAATACAGAAT	161436
rs376354876	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88755019	CACATTGGCCAGGTT[A/C]GTCTTGAACTCCTGA	161436
rs376367098	snp	G/T	0.000169986	0.00921759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714963	TATAAAAAAGTCTTT[G/T]CCCATTTCCATCATT	161436
rs376367523	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651237	CCCTCTCTCTCCCTC[C/T]CCACACCTTGTCATT	161436
rs376370920	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88629924	TAGAGATGCCATAAG[C/T]GTCTCTTTAAATTTT	161436
rs376380923	snp	A/G	4.96866e-05	0.00498406	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626946	GGTCCAGAACTTCAC[A/G]TGTTTTACTCCCACT	161436
rs376386341	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88660521	GTCGAAGTGGGCGGA[A/T]CACAAGGTCAGGAGT	161436
rs376396482	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785020	TCAGCCATAAAAAAA[C/T]GAGATCCTGTCATTT	161436
rs376398614	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88742224	CAAATCAATATTGAC[C/T]AATAGAAATTTCAGT	161436
rs376401655	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710545	TCAAGGTATGTAATT[A/G]TGTGAATTCAATTAA	161436
rs376439317	snp	A/G	1.68145e-05	0.00289948	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702478	AGTCTTTCAAAGGAT[A/G]AATAGTTAGGCAGAG	161436
rs376455326	snp	C/T	1.66164e-05	0.00288235	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616167	CACCTCCAGCACTAA[C/T]AACATGTCGATCACC	161436
rs376463554	snp	A/C	7.30647e-05	0.00604376	intron-variant	EML5	GRCh38.p7	14:88715237	CATGAACAGAAGTCA[A/C]AACAGAATTAATGCC	161436
rs376499925	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88791189	AAACAGAAGAACAAC[C/T]TTATTTGTGGAATTT	161436
rs376512420	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769323	CACCTCGCTTCCTTC[C/T]ACTCTAGCCATGTGA	161436
rs376543540	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88687681	ATGGTAACTACCTGA[-/A]TGGATATGGTGATTA	161436
rs376557881	snp	A/C			upstream-variant-2KB	EML5	GRCh38.p7	14:88793222	CGGTTCCGCACGGTC[A/C]CTGCACCCAGCGTAG	161436
rs376567607	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746016	CAATACATATGTACT[C/T]TAACACTTTAAGACT	161436
rs376621356	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88769722	TTCTATAGTCTGTAT[A/T]CATAGATACATTCTG	161436
rs376621538	snp	C/T	0.000310357	0.0124532	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657386	ATTACCTTTCATCAA[C/T]TGAGGGTTCTTTTTG	161436
rs376663835	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88621473	TGACTACAGGCACAC[A/G]TCTATCTGTAAGCAC	161436
rs376700332	in-del	-/GTT			intron-variant	EML5	GRCh38.p7	14:88780384	ACAAAGGGTAGATTT[-/GTT]TACTGTTCAGTATAA	161436
rs376716304	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721707	CAGGTCATGGGCATG[C/T]GCAAAGATTTCATGA	161436
rs376723513	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88787989	ATTCCTGGGCTCCAA[A/C]CCTAGAAGATTCTGA	161436
rs376749476	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88753264	TGAGCTGGGCAGCCA[A/C]CTAAACGAGCTACAC	161436
rs376756342	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88645517	CAGGTATTGAATACA[A/T]CCTTCTTGAAAGTGA	161436
rs376771776	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88773375	TGGTAATAAATCTCC[A/G]AACAGGGAATATCCA	161436
rs376775192	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88742920	CAGAACCTTAATTAA[C/T]TCACTAGGAATTAAC	161436
rs376786583	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619405	TTTTTTAAATAGAGG[C/T]GGGGTCTCACTATGG	161436
rs376792888	snp	A/C/T	5.63834e-05	0.00530934	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754628	AAGGCTCTTTCCCAA[A/C/T]TTGTCCTGTTGCTAC	161436
rs376801166	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727586	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	161436
rs376828587	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88640239	CACTCTGCCCATCAA[C/T]CATAGAATATACATT	161436
rs376830332	snp	A/C/G	6.79186e-05	0.00582707	intron-variant	EML5	GRCh38.p7	14:88618830	GAATCAAAACAAAAC[A/C/G]TAAAAAGTATTAGAC	161436
rs376847921	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88699886	TATTTATCTCCATTT[C/T]AGATATGTTGAATCT	161436
rs376863319	snp	A/G	1.66585e-05	0.00288599	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622624	CTCTGCACACAGAAC[A/G]AACACAATCTGTGGC	161436
rs376875950	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617506	GGGTCCAGCAGCACA[C/T]ACCAGTAATCCCAAC	161436
rs376896024	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88666415	ATTTTTAGTAGAGAT[G/T]GGGTTTCACCATGTT	161436
rs376930401	snp	A/T	0.000215662	0.0103819	intron-variant	EML5	GRCh38.p7	14:88621321	AACACAAGCAGGACC[A/T]ATACAGTGAATGTAA	161436
rs376939186	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88701705	CTAGAAGGTATATTT[A/G]CACAGTGTTTAAAGC	161436
rs376949605	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88737528	CAGGGGCATTGCGCC[C/T]GCCATGGAGGTCTCC	161436
rs376967962	snp	A/G	0.000135217	0.00822134	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792282	GGCTTGCAGGGTGAC[A/G]GCGGCGGCCCCCGCT	161436
rs376973715	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710301	TCTTTGAGCTAACTT[C/T]GTATATTTTTTGTTT	161436
rs376978825	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88696233	CACTTCAGTCAGAGC[A/G]GCAAAAGCATTAATT	161436
rs376993243	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88717783	CAACAACAACAACAA[-/C]AACAAAACAAATTAA	161436
rs377011639	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88717581	TAACACGGTGAAACC[C/G]CATCTCTACTAAAAA	161436
rs377011836	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763076	GATCTAAAATCGACA[C/T]CCTAACATCACAATT	161436
rs377019895	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780522	ATGACTGTGAGGATC[A/G]ACAGGTCTAAAATCC	161436
rs377059840	snp	C/T	5.21082e-05	0.00510406	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627651	AGAATCCTACCTTCC[C/T]GCCATCTCCAAATGG	161436
rs377060945	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88619751	GATGGCGCAACCTCC[A/G]CCTCCCGGGTTCAAG	161436
rs377074103	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88667692	TGACTCCCTTCCTCC[A/T]GTGTGCTGTTTTACT	161436
rs377082747	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619819	ACAGGCGCCTGCCAC[C/T]ACGCCCGGCTGATTT	161436
rs377091178	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671253	CACTAGGGGCCAATA[C/T]TCAACATTCTTAAAG	161436
rs377120129	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636302	CCATGGAAAGCAATC[C/T]CCTTGCTCTCATGTA	161436
rs377149606	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88714558	AATGTTCTCACCACA[C/T]ACACACAAAAATGGT	161436
rs377154150	snp	G/T	2.11629e-05	0.00325285	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661654	AAGAAAAACACATAC[G/T]TTAGTAGGATATCTA	161436
rs377183047	snp	A/G	3.31521e-05	0.00407123	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616813	TGAATGAGATACACA[A/G]GCACAGTTGACATCA	161436
rs377200302	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88730720	AGTCTGCATGAAACA[A/G]CTAGAGACAAGAATA	161436
rs377256906	snp	A/T	0.000151057	0.00868941	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705570	TCTGATTCATCACTA[A/T]GAGAGTCAGCCAGAC	161436
rs377258259	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88676707	AAAACAAAGCTGGAG[A/G]CATCATGCTAATCCC	161436
rs377274354	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721425	AAAACAGATGGGTAG[A/G]CCAATGGAACAGAAT	161436
rs377359931	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690814	TGAGTAGATGAGAGA[A/G]AGAATCTAGTGCACA	161436
rs377378341	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706764	TAATCAACTAGACCT[C/T]ACCCCCATTATTCTC	161436
rs377392149	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617374	CTAGTCTCGAACTCC[C/T]GACCTCAGGTGATCA	161436
rs377399976	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88626127	TAAGCAGTGTGTTAA[A/G]TGATAAAAAGCAAAG	161436
rs377441539	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676446	ATCACGAGAACAGCA[C/T]GGGAAAGACCTGCCC	161436
rs377450270	in-del	-/GA			intron-variant	EML5	GRCh38.p7	14:88704513	AGACAGAAAAAAAGA[-/GA]CACAGAGAGGTTAAG	161436
rs377456271	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88641262	CTAACTCATTCTGTG[A/C]AGCCAGCATCACCCT	161436
rs377459724	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88632924	AAGAAGCAGGTTCTG[G/T]GTAATCCCTGGCATG	161436
rs377472523	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651154	CTGCCTTGTCATTTT[C/T]TTTTTTTTTTTTTTT	161436
rs377475806	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88655283	ACCAAAACAGATATA[C/T]AGACCAATGGAACAG	161436
rs377476002	snp	A/C	8.39581e-05	0.00647858	intron-variant	EML5	GRCh38.p7	14:88685153	AAGACCTGAAATGTT[A/C]AATGAAGATGTTCTT	161436
rs377525336	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88650215	CCCAGCACTTCGGGA[A/G]GCTGAGGTGGGTGAA	161436
rs377566563	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88790180	CTTTCACTGATTCCT[A/G]AATTATATTCTCAGT	161436
rs377568249	snp	C/T	4.55591e-05	0.00477258	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88694377	CACATAGGGGTTCAT[C/T]TTTACAACAAAAATC	161436
rs377569250	snp	A/G	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88755724	AAGGCTGGGTGTAGC[A/G]GCTCATGCCTATAAT	161436
rs377576340	snp	C/G	3.33739e-05	0.00408483	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618246	GTCCATGTAGCCCAA[C/G]TAATTCTGTCAATAG	161436
rs377578583	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88662370	TTTTTTTTTTTTAAA[A/G]AAGCAAAAACAGTAA	161436
rs377612150	snp	C/T	1.6861e-05	0.00290348	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661722	GAACCATTTTGTCAC[C/T]GGTGAGGCAAGAAGC	161436
rs377613436	snp	C/T	0.000173985	0.00932536	intron-variant	EML5	GRCh38.p7	14:88726682	AGGCTCCATATCCTG[C/T]AAAATTTAATTTAAA	161436
rs377659428	snp	C/T	0.000363143	0.0134699	intron-variant	EML5	GRCh38.p7	14:88740585	GAACTAAAAGGTATA[C/T]AGTATAATCAAATTA	161436
rs377662889	in-del	-/A	0.437683	0.165152	intron-variant	EML5	GRCh38.p7	14:88670319	GCAGGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	161436
rs377704674	snp	C/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88691654	CCTAGATCTGGAATG[C/G]GAGGCAAGAAGCCCC	161436
rs377732469	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88636558	CCCAGCTACTCAGGA[C/G]GCTGAGACAGGAGAA	161436
rs377740933	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88702693	CTGATCAATACAGAA[A/T]ATACAGGGGAGAAGT	161436
rs377747484	snp	A/G	1.66479e-05	0.00288508	intron-variant	EML5	GRCh38.p7	14:88736340	TACATTCCAGCCTAT[A/G]GAATTAGTTTATAAT	161436
rs377759733	snp	A/C			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765851	ATTTGTTTTAAGAAC[A/C]GTTACTTCATGGCAT	161436
rs377761750	snp	C/T	0.000267939	0.0115714	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661765	AACTTCTCCAATTAC[C/T]GGCCAAATTCCTTCA	161436
rs377763414	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88786756	TTTTCTCGTGCTGCC[A/G]CCATGTAAGAACTGC	161436
rs386382093	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88623018	CTCTCTCATAATACT[-/T]TTTTTTTTTTTTTTT	161436
rs386382094	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88623032	TTTTTTTTTTTTTTT[-/TT]TAAGATGTAGTCTCG	161436
rs386382096	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88727402	TGTGATACACTGCAT[-/TT]TTTTTTTTTTTTTTT	161436
rs386382097	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88727417	TTTTTTTTTTTTTTT[-/TT]TGAGACGGAGTTTCG	161436
rs386779766	multinucleotide-polymorphism	GTTAGATCATCAAGGTAGAAA/TTTCTACCTTGATGATCTAAC			intron-variant	EML5	GRCh38.p7	14:88640142	CAACCCACTGATAGT[lengthTooLong]ACTAACAAAGAAATT	161436
rs386779767	multinucleotide-polymorphism	GC/TT			intron-variant	EML5	GRCh38.p7	14:88640397	TCAATACCAAGAAGA[GC/TT]TCCCAAAACCACACA	161436
rs386779768	multinucleotide-polymorphism	CGC/TGA			intron-variant	EML5	GRCh38.p7	14:88668016	TCTGGCAAGCTTTTT[CGC/TGA]CACAAGCTCACTGAA	161436
rs386779769	multinucleotide-polymorphism	CA/TG			intron-variant	EML5	GRCh38.p7	14:88697896	ATGTGCCACCACACC[CA/TG]GCTAATTTTTTGTAT	161436
rs386779770	multinucleotide-polymorphism	CA/TC			intron-variant	EML5	GRCh38.p7	14:88714249	TTTTTGACTAAGATA[CA/TC]GTGGTACTTTACCAT	161436
rs386779771	multinucleotide-polymorphism	AT/GC			intron-variant	EML5	GRCh38.p7	14:88742563	AAACCTGAAAATGGA[AT/GC]CTTTAGCTTTACTTA	161436
rs386779772	in-del	A/GT			intron-variant	EML5	GRCh38.p7	14:88790366	TCGAGTATGTTTGTT[A/GT]TTTGTATAAGTTGTG	161436
rs397695528	in-del	-/TTAT			intron-variant	EML5	GRCh38.p7	14:88707307	TATTTATTTATTTAT[-/TTAT]GGCAGAGACAGGGTC	161436
rs397707614	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88731329	CAGTGTTTGGTTTTT[-/T]GTCCTTGCGATAGTT	161436
rs397719888	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88622815	GAATCTTTTTTTTTT[-/T]AAAAAGGCCCTGATA	161436
rs397770215	in-del	-/T			intron-variant, utr-variant-3-prime, frameshift-variant	EML5	GRCh38.p7	14:88616055	TTGACTAGCTGATTT[-/T]CATAAACCAAAGCTG	161436
rs397772247	in-del	-/A	0	0	intron-variant	EML5	GRCh38.p7	14:88777248	GCAGAAGACTTTACA[-/A]GTGGAAACCTTACAA	161436
rs397794390	in-del	-/T	0	0	upstream-variant-2KB	EML5	GRCh38.p7	14:88793790	AAAATCGAAGTACAA[-/T]TTTTTTTTTTTTTGC	161436
rs397797340	in-del	-/A/AG	0.5	0	intron-variant	EML5	GRCh38.p7	14:88620951	AAAAAAAAAAAAAAA[-/A/AG]GAGTCATAGGAAACA	161436
rs397800679	in-del	-/A	0	0	intron-variant	EML5	GRCh38.p7	14:88618021	TCCTTAAAAAAAAAA[-/A]CTTGATAAATCATGG	161436
rs397830753	in-del	-/CATT			intron-variant	EML5	GRCh38.p7	14:88684533	ATTTTAGCATACATT[-/CATT]TTTATTTTTTCTTAG	161436
rs397852197	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88630025	TAATAAAAACTGTAT[-/T]TTTTTTTTTTTTTTT	161436
rs397945208	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88630047	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCGC	161436
rs398026076	in-del	-/TGTATTCAACTATAT	0	0	intron-variant	EML5	GRCh38.p7	14:88663468	GATGTTATTGTTTCA[-/TGTATTCAACTATAT]TGTATTCAACTATAT	161436
rs398026077	in-del	-/T	0	0	intron-variant	EML5	GRCh38.p7	14:88664290	TTCCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	161436
rs398026078	in-del	-/A	0	0	intron-variant	EML5	GRCh38.p7	14:88693788	CAAGAACTTGTCTCG[-/A]AAAAAAAAAAAAAAA	161436
rs398026079	in-del	-/T	0	0	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767887	GGAAAAAATGGTGAA[-/T]TTTTGAATAAGGTTT	161436
rs398026080	in-del	-/T	0	0	intron-variant	EML5	GRCh38.p7	14:88773825	GGCCCCAGTAATAAG[-/T]TTTTTATCACCTCCA	161436
rs398039203	in-del	-/A	0.5	0	intron-variant	EML5	GRCh38.p7	14:88751516	AAAAAACCAACAAAC[-/A]AAAAAAAAACTCTTC	161436
rs398043944	in-del	-/TA	0.5	0	intron-variant	EML5	GRCh38.p7	14:88689326	TTTCCGAAGTTTATA[-/TA]CCAATGTACACTCCT	161436
rs398057356	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88631167	TCAGAGACAAAAGAT[-/AT]TCCCATAGTGTCCAC	161436
rs398077945	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88674825	CCTAGATACAATGGG[-/G]GTACAGGCATTGGAT	161436
rs398118494	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88619697	GAATTTTTTTTTTTT[-/T]GAGACGAAGTCTCGC	161436
rs398118495	in-del	-/TA			intron-variant	EML5	GRCh38.p7	14:88729101	TCATATATATATATA[-/TA]ACCAACTGAGAATGG	161436
rs527237375	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88785260	TTAGAATGAATAAGA[C/G]CATTTGATGGCACAA	161436
rs527243709	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650069	CTAACTTATGTCACA[C/T]TGGTTTAAACATTGA	161436
rs527265995	in-del	-/AAC	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88726155	CATAAGGCTGTAAAT[-/AAC]AACAACAACAACAAC	161436
rs527305364	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88754383	CAACCTCCCACCCCA[C/T]CTACCCACCTCCACC	161436
rs527305957	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88649256	GTCTAGGCTGGTCTT[C/G]AACTCCCAGGCTCTA	161436
rs527307894	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657611	TAAATTAAGTTGTTA[C/T]AAGCAAATTATGAAG	161436
rs527336873	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762670	GCAGACCTAACAGAC[A/G]TTGACAGAACTCTCC	161436
rs527343626	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700645	TTAGAACAGAGTTTT[G/T]AATCACATCTGTCTA	161436
rs527369665	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708341	TTACCCCTTGTGATT[A/G]TATTTATATAACACT	161436
rs527385040	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758349	AGGCATGCACCACCA[C/T]GCCCAGCTAATTTTT	161436
rs527407804	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715908	TGGAACTTTTTTTCA[A/G]TGATGACTTCTTATT	161436
rs527414870	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665157	TAGTAACAGAATTGG[C/T]GCTAAGACAGATATT	161436
rs527417541	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656837	TTCTTAAAAAGTACT[C/T]GGTATTGGATTCAAT	161436
rs527421471	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761294	GTCATGGTGGTTTGC[C/T]GCACTCATCAACCTG	161436
rs527447696	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88626119	CTGTATGATAAGCAG[G/T]GTGTTAAATGATAAA	161436
rs527455447	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88731177	TGCACTCATTAACTC[A/G]TCATTTACATTAGGT	161436
rs527457673	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88726764	ATAATCTCATCTTAA[A/T]TAAGATAAATCTAGA	161436
rs527484446	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88730155	GCACAATGGAGCATG[C/G]ACTATACTGTTATTG	161436
rs527496194	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88693973	AGACAGGGTCTCACT[A/C]TGCTGCCCAGGCTGC	161436
rs527514064	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688146	GAAAGGTCAAGATGA[C/T]CCTAGCCCACAGACT	161436
rs527546733	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690097	CAAGTGCAAAGGCCC[C/T]GATACAACAACATGA	161436
rs527550705	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694578	ATTTTAATATGGTAA[C/T]TCTGCTCAAGAGAAT	161436
rs527555287	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783545	ACCAGAAAAAGTAGA[C/T]TTGAAGTAAAAAAAC	161436
rs527568086	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643901	CTTGTTTACGTTTGA[G/T]TTAGCAGAGTTTGGT	161436
rs527595910	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792177	TGGACTCGGGACCAG[A/C]GAGACAGCTGCGGAT	161436
rs527598245	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693849	GATCACAGCTCACTG[C/G]AGCCTTAACCTCCTG	161436
rs527626155	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88737524	GGGACAGGGGCATTG[C/T]GCCCGCCATGGAGGT	161436
rs527660837	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678638	TAATACCATTATTTC[A/C]AAATTTTAAAAAAAT	161436
rs527696866	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735995	TTTAATCGGAGTATT[A/T]TTTCTTTCTTTTTTT	161436
rs527703132	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628194	ATATTAAACAATAAA[A/T]ATTAAACACCAAGTA	161436
rs527724326	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685442	CCATCTCCTGCCCCT[C/T]TTATTTACAATATTC	161436
rs527752095	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692290	GCTGAGGCAGGAGAA[C/T]CACTTGAACCCAGGA	161436
rs527766609	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88640861	AAACACAATAAAAAA[C/T]GACAAAGATCACATT	161436
rs527786298	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630709	AGGCTAAAATGACTC[A/G]GTCAGGCTAAACGGA	161436
rs527790040	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699035	TATCACATTCCATGA[A/G]GTATAGACAGTATTT	161436
rs527834373	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743655	AGCCAGGTCTACTCA[C/T]GTTGCTTCTCCCACA	161436
rs527837701	snp	A/C	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715113	CATTGCATCCAACAG[A/C]AAGGTAAGTTCCATC	161436
rs527851983	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660116	CCCCATCTCTACAAA[A/T]AAAAATTTTTTTTTA	161436
rs527876629	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664359	GTAAAATAGTAAAAA[A/T]TAATTTTGAGAATAA	161436
rs527879741	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762233	ACAAAGACACGGGCC[A/G]TGCGTAGTGGCTCAC	161436
rs527879809	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88769343	TAGCCATGTGAAGTG[C/T]CTTGCCTCCCCTTTG	161436
rs527889067	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671605	TAAAAGACAGAGAAT[A/G]GCATGCTGATAAAGA	161436
rs527902325	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678387	AGCCATCATGGCACA[C/T]GTTTCCCTATGTGAC	161436
rs527907574	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88617633	TGACTTATGACATAG[C/G]AATTAAAAAAATTTC	161436
rs527943700	snp	A/C	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774844	TACCAGCTCAGATTG[A/C]TTCCCTGAATTATAG	161436
rs527957265	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670681	CCATGATAAAACATT[A/G]CAGGAGCTGTTAACC	161436
rs527975976	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88722750	GCTCAAGGTCATTGC[C/T]AAGGTCTGATTTTTC	161436
rs527977172	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88634955	AGGGAAGAATTAGAT[C/T]TAAACCTTCTGAGCT	161436
rs527985229	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766903	ACCCACGTTGAGTAT[C/T]GGGGGCTGGTTTCCC	161436
rs527989903	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774294	CACACTTTTCAGAAG[A/C]AACGATCCAGGGCTG	161436
rs527994700	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624459	TTGGGAGATTTGAAA[A/G]TCACTCAGAAGAGAC	161436
rs528012956	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768561	AATTACAGGTGCCCG[C/T]CTCCACACCTGGCTA	161436
rs528012963	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729927	ATACTGTCTTTGTAT[C/T]ACACTACAGAGGCAG	161436
rs528025012	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88722092	TCAGTCAGAATGACA[A/C]TTATTAAAAAGTCAA	161436
rs528047513	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88638620	TCAAGACCAACTCAG[A/G]TAACCAGAGTGAGTG	161436
rs528063804	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733402	GTCAGTTCTTTGAAG[C/T]TTTTAAGGTGATTGA	161436
rs528068923	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88772150	GCTAAATTTCATCCT[A/C]ACTACTTATCTTTTC	161436
rs528089709	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663387	ATTCCTAGAAACAAA[C/T]GTTAAAATATTTTTT	161436
rs528100096	in-del	-/A	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88769637	TAAAACCTTATTTAC[-/A]AAAAAATAGGTGACA	161436
rs528118220	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682768	CCAGCCCCTCCTCCA[A/G]ATGGAGGCTCTACTT	161436
rs528148231	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88647472	GAGGCCAAAGCAAGA[A/G]GATTGCTTGAGCCTG	161436
rs528177587	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88637985	AGACAACAAATTCCT[G/T]ACTATCAACTTAGTA	161436
rs528184131	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689043	ATGATTTGTTATAGA[A/G]TTTTTTACATGTTAG	161436
rs528234633	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740240	TTCTTCATTGAAATC[C/T]TGAAAACAAATAGAT	161436
rs528238306	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645183	AGCGTGCACCACCAC[A/T]CTCAGCTAATGTGTG	161436
rs528266399	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668851	AGGGGAGCAGAAACC[A/C]AGAGCAAAAAAGCCA	161436
rs528276501	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758477	TGGGATTACAGGCAT[A/G]AGCCACCGCGCCTGG	161436
rs528282669	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613203	TGAAACACGAGAAGC[A/G]GCAAAGACAGAGCAC	161436
rs528316681	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614673	ACTACAGATAGGCTA[C/G]ACAGCGAATTCCTGA	161436
rs528338612	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675743	GCAAATTTCCTGAAC[A/T]TTTATGCTCTGGTTC	161436
rs528342511	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667816	CTGTAATGGCTCTAA[A/C]AATTTAGCTGCAATT	161436
rs528362905	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88701743	ACTGAAGGCTTTAGG[C/T]TTTACTACCTATTAA	161436
rs528382048	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719466	GGAAACCTTACTCCA[C/T]CTTCAGCATAATTCA	161436
rs528387099	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88629994	CTTTATCCCCTAGTT[A/T]GCCTTTGATGCAGTA	161436
rs528388106	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88726881	CTTTTGCTTTGAATT[C/T]TTTTGGCGACATCAC	161436
rs528396799	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88622045	TCCCCCTCCCCCTTG[C/T]CCGCCTCCAGTAACC	161436
rs528420139	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88751801	AGAGGGAGAAAGAAA[A/G]CCAGATAAAGAAGCC	161436
rs528426284	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727089	TTTTAGCACAGTTAT[A/G]GTGTCACTGCATAAT	161436
rs528456841	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709590	AAAAGTTAGAAAGTA[C/T]AGCAATATCAAGTGC	161436
rs528457979	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658534	AAATACTGAAACTCA[A/G]CAGAATAAAAGATAC	161436
rs528459743	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764175	TTGAGAATTTTTACA[A/T]CTATATTAATGAGGG	161436
rs528481533	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666172	TTGCAGAGTAGGTTT[C/T]ACCTTTGTAGCTTCT	161436
rs528494860	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673576	CCAATAGGAAGAGAG[A/G]AAGTAAAACTGTTTT	161436
rs528496351	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88620522	GTGTTAACATGAATT[A/C]ATCAAACATTACCTA	161436
rs528551178	in-del	-/CAAA	0.00143859	0.026781	intron-variant	EML5	GRCh38.p7	14:88702397	TAATTTATTTAAACT[-/CAAA]CAAAGGTGTAGCTTA	161436
rs528555067	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627570	CCACCAACTTTAAGA[C/T]AAATATTAAATACAG	161436
rs528566650	snp	C/T	3.32568e-05	0.00407766	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626855	CACCAAATGCAATAG[C/T]GAGCATGGTCTGCAT	161436
rs528571263	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88717041	TGAACAGTTCATAAT[A/T]CATCACAAAGTAAAG	161436
rs528611389	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724765	CATAAGTAATGACCA[G/T]GTGTTTCTATTTATT	161436
rs528622533	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652479	AACTCAAATCCCTCT[A/G]ACGAAGCTTTCCTGT	161436
rs528638936	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88644920	TTTCACCATGTTGGC[C/T]AGGCTGGTCTCGATC	161436
rs528655333	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653507	GTTTTTAGCATGAAG[A/G]GGTGCTGAATTTTAT	161436
rs528678591	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617437	CAGGCTGAGCCACCG[C/T]GCCTGACTGAAAACT	161436
rs528679384	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88739330	GATGCAAAACCCATA[C/G]ATAGGGAGGGCTTTA	161436
rs528682792	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651763	TAAATACATATGTAG[C/T]GCTTATTGCTTTGTG	161436
rs528698201	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747240	AACACGTTGAAACCC[C/T]GTCTCTACTAAAATT	161436
rs528715332	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88620507	AATGGACATGGCTAA[A/G]TGTTAACATGAATTC	161436
rs528725156	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695578	ATGTTAAATGTTAGG[C/T]ATGCATACACCTATA	161436
rs528735258	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756338	ACACATAAACTAGAA[A/T]CTGAAGGAAACTTCC	161436
rs528793189	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659148	TAAAGCAGGTTTTCC[A/G]TTAACATCTTTTCAA	161436
rs528814338	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710159	CAGAGAGATTATGGT[C/T]AAGAGCAGGTGAAAC	161436
rs528842146	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761314	TCATCAACCTGTCAT[A/C]TACATTAGGTATTTC	161436
rs528867524	snp	C/T	1.7364e-05	0.00294647	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715090	TCCATAAATATCAAC[C/T]GAGCTGTCATTGCAT	161436
rs528875088	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663309	AACTAAATTCATAAG[C/T]GGTTTGATTTTTGTA	161436
rs528878423	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88760616	TCCTCTACCTTTGTT[C/T]TTTTTCCAAATTGCT	161436
rs528882514	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88617099	GGGTTTCTAGATTAA[C/T]CTTTTTAAGATTAAA	161436
rs528888456	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88662628	GCTCACTGCAGCCTC[C/T]GCCTCCTAGGTTCAA	161436
rs528900729	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767471	CTAGGATGTTAGCCT[A/C]TGCATACTATCATAT	161436
rs528902367	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670343	AAAAAAAAAGGAGAA[A/G]AAAGAAAAACAAACA	161436
rs528940598	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766963	TACATTCTTTCATAA[A/G]TTCAACATGTAGGTC	161436
rs528944318	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624217	GAGTAGCAGGGACTA[C/T]AGGCATGTGCCACCA	161436
rs528964251	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669625	AGGGGAGGGGCATCC[A/G]TGGTCTCCATGGATC	161436
rs528975491	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88721934	AAGAAAAAAACAACC[C/T]CATTAAAAAGTGGGC	161436
rs528988265	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729537	TAAAGTTTTATGGAA[A/G]TATAGGCATATACTT	161436
rs528993527	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88791062	AGCACCACCTCATTC[C/T]TTACTCTGCAATCTC	161436
rs529006749	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649098	GTAGTGATGCCATCA[C/T]AGCTCACTGCAGCCT	161436
rs529027873	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700469	GCATCCCTGAGTTAT[C/T]TTCAGGAAACAAAGC	161436
rs529060806	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88752978	ACACCACCCTTCAAT[C/G]TGTTCGTGTAACCTG	161436
rs529067025	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88648467	CCAGACATCTTCCTG[C/T]CACAGCATCCCACGT	161436
rs529094968	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88673042	ACTCATTTTTTGAGG[C/T]CAGCATGATCTTGAT	161436
rs529099790	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656471	GGGGCCTGTCAGGGA[A/G]TGGGGAGCTAGGGGA	161436
rs529163451	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88655207	AAAGCTGGAGGCATC[A/G]TGCTAGCTGACTTCA	161436
rs529175152	snp	A/C	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88669184	GGTGGATCAGGAGAT[A/C]CCCTCCGTGAGCCCA	161436
rs529190298	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707337	CTTGCTATGTTGCCC[A/T]GGCTGGTCTCGAACT	161436
rs529199391	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655593	TGACTAAAACACTGA[A/C]AGCAATTGCAACAAA	161436
rs529255449	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88741735	AAAAATAAACCAAAA[A/T]AATGGGACAGGGCAG	161436
rs529256613	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646318	GTAAAATATATAAGC[A/G]TGACTGGTGTCATAA	161436
rs529295553	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88750248	TATTTAGCCTCCCTG[C/T]ACCTTACTTTCTTCA	161436
rs529321283	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653860	TGTTTGGAATAGCCA[C/G]AAGAATGGTACCAGC	161436
rs529324395	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695992	ATCAGTGAATATCCT[A/G]TGGGTGTGCATGTTT	161436
rs529335305	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88768895	GAGAGTAAATGTTTT[A/C]CGCTCTGTGGGCCAT	161436
rs529364104	in-del	-/TC	0.00280955	0.0373749	intron-variant	EML5	GRCh38.p7	14:88661096	GATAAAAGGAATGTG[-/TC]TCTCTCTCTGACACA	161436
rs529373980	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88772480	GATATACCTTCGGCC[A/G]GACGAGGTAGCTCAT	161436
rs529393681	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88712574	TAGTAAATTCCAAAA[C/T]TTAATGTATCTTCCC	161436
rs529397804	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88661177	CACTGTAGCCTCCAA[C/T]TCCTGGGCTCAAGCA	161436
rs529413132	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749346	AGCAAAAATATCCTT[C/T]GAAAATTGAGTCAAA	161436
rs529420666	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615246	GTCCTTTATAAAAAA[A/G]GACCTTATTAATGCC	161436
rs529448003	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88746812	AAGCAGTAAACCTCT[C/T]GGAAACAACAAATAA	161436
rs529453582	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735128	TCAATTCCTAAATTT[C/G]ATCAGTGGTTCTCAA	161436
rs529504587	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684595	GAGAAAAATAATTGC[C/T]TTAGGCTCAACAAAT	161436
rs529535114	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728055	TATAGCTGAAACAGT[A/G]CTTAGGAGGAACTTT	161436
rs529545045	snp	C/T	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684237	AATGGAAGTTAAAAA[C/T]TCGGCTCACTGCAAG	161436
rs529548042	snp	A/C	0.0248432	0.108648	intron-variant	EML5	GRCh38.p7	14:88640158	TTAGATCATCAAGGT[A/C]GAAAACTAACAAAGA	161436
rs529565743	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88631056	TGCCTGTCACTACAA[A/C]TACTACCAGAGAGTG	161436
rs529600742	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690827	GAAAGAATCTAGTGC[A/G]CAAATGGAAGAACTG	161436
rs529623911	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88738163	AACTAATGAAAATAA[A/C]ATACCAATTAACATT	161436
rs529630619	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639654	TAATCCTGGCTCATT[A/G]CAACCTCCACTTCCC	161436
rs529642283	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88617272	CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATCA	161436
rs529662212	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88647171	TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAT	161436
rs529666239	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644035	ACAGGCTTCATGAAC[C/T]CTGTACAGTGAATAT	161436
rs529689809	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694648	ACAGCATCTATAATA[C/T]CTACTATAGTACTGT	161436
rs529701305	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793189	GCTGCTTTGCGTCCT[C/T]AACCGGGAAGCACCT	161436
rs529726648	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701352	TGCTAAGGTATTGTC[A/G]TAAATATAGATCAGA	161436
rs529818924	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88769174	CCAACCAAATCTCAT[A/G]TTGAAATGTAATCCC	161436
rs529846311	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770868	ATCCATATTGTGACA[C/T]TATCATCTGAAATAT	161436
rs529862501	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627647	CAAAAGAATCCTACC[C/T]TCCTGCCATCTCCAA	161436
rs529882455	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88788784	GCACTCTGGCTGCAC[A/G]CGGTGGCTCACATCT	161436
rs529890175	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673731	CATTCCTATATACCA[A/C]CAACAGAAAACAGAG	161436
rs529910355	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777979	CATCCTGTCTCAAAA[A/T]ATACAGCAAATTTTT	161436
rs529929869	snp	G/T	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88731826	GATGGCCAGTGATGA[G/T]GAGCATTTTTTCATG	161436
rs529947850	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88777317	GTAAAAAAAAATTTA[C/T]CCTAGAATAGTATAT	161436
rs529950386	snp	A/T	1.92406e-05	0.0031016	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695371	CCTACCTTGCTATTG[A/T]AAGTTTCTCTCCTTT	161436
rs529957575	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88688194	GCAAGTAGAAAGGCA[C/G]TGTTCCTTTACTTCT	161436
rs529984949	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88636179	CACTGGGAGGACAGA[C/T]GCAGAGAAAAGGCTC	161436
rs529987060	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690333	CTTCTGGATTGAGAA[C/T]AGATACAAGGGAGGT	161436
rs529988257	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88785309	TAATAATTTAATTGT[A/G]CATTTTAGAATAACT	161436
rs530009021	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794182	ATCGTTTCAAGAAAT[A/G]TGACTCCAAAAGGGG	161436
rs530012247	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671738	GAAAGCAGGAAAAAG[C/T]AGGGAGTGCAATCCT	161436
rs530014144	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88680114	ACAGCTATACTTATA[C/T]TATGATTTTGTCTTT	161436
rs530024835	snp	A/G/T	0.00159649	0.0282165	intron-variant	EML5	GRCh38.p7	14:88784469	CATTACAACTGATAC[A/G/T]GCAGAAATTCAAAGG	161436
rs530032247	snp	A/G	0.000203039	0.0100736	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738892	ACCTTTGTATCCCTG[A/G]TCTGTTTCCCTGAGA	161436
rs530035276	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775384	GCAGAAGGGAGCCCA[C/T]TGCCCTGAAAAGTGA	161436
rs530054229	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644734	TATTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	161436
rs530068754	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88783214	AAATGTGGGGTTGGA[G/T]CCCCCACACACAAAT	161436
rs530070511	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88722841	GGTGCAGCAAACCAC[C/T]GTGGCACATGTTTAC	161436
rs530070695	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730692	GAAGTGACAAGAATT[C/T]GCTTTTATGAATAGT	161436
rs530075299	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679257	GGTTAGAACTTCAAC[A/G]TATCTTTTCAGGGGG	161436
rs530084192	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88693218	ATTCTTTTGCAAGTA[A/T]GAATACTACTGTATT	161436
rs530102912	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88782801	TGAAAATGCCTGGAT[C/T]GGGCACGGTGGCTCA	161436
rs530133057	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661923	TTTGTAGTTATGTGT[A/G]TCACAAGTAAAATGA	161436
rs530143502	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88791052	CTGAATACAGAGCAC[C/T]ACCTCATTCCTTACT	161436
rs530147946	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693199	GATTAATCTCATATA[C/T]TGAATTCTTTTGCAA	161436
rs530148575	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88687030	TTACCATGTGTATCA[C/T]AGAAAATAGACTTTT	161436
rs530171131	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88642137	TCAATCTACTCTTTA[C/G]CCATTCAGGATGAAG	161436
rs530205242	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737296	GGGCTTCAGGGCCGC[C/T]AGAGTCCCCAAGTTT	161436
rs530208653	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730034	CACAGTTACAACTTG[A/G]CAGAATTTTGAGGGC	161436
rs530225671	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657677	TTTAATTATATGTAA[C/T]GATGTTTTCAAAGTA	161436
rs530270864	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708485	ACTCATTAGATATTT[C/G]AAGAAAGAGAAAAAG	161436
rs530293159	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769401	AGCCTCCCCAGAAGC[A/T]GAAACTGCTATGCTT	161436
rs530293725	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672332	AAGGCAGAGATCAAG[A/T]AGTCCTTTGAAACCA	161436
rs530299095	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763609	CCATTCCTTCCAGAA[C/G]ACTTCCAAACAATAG	161436
rs530306750	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88715981	GGATAAATATGTAGT[A/T]AAACACCACGGAGTT	161436
rs530309023	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666013	TCTATAGAAGTCAAT[A/G]GTATGGAATTCTAAG	161436
rs530390956	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630804	GAAGCACATAACTCC[A/G]ATTGCTACTGCAGCC	161436
rs530397026	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88708184	GTCAATGGGACTGTA[C/T]TAATTTTTTAATAAC	161436
rs530401244	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676672	AAGAGCCCATATAGC[C/G]AAGACAATGCTAAGC	161436
rs530416772	snp	C/T	0.000105781	0.00727181	intron-variant	EML5	GRCh38.p7	14:88618858	GACCACATGAAGTAT[C/T]ATAAATACTTAAGAT	161436
rs530434401	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88625956	GATGTGGATTGGAAG[C/T]CACAGGTCCAGATGA	161436
rs530457296	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779740	TTTATCTTGAGGAAT[G/T]AATTTTAAGACCAGA	161436
rs530468451	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719641	TCTACTTTAAAATAT[C/T]TGCAAGTTTTCATAT	161436
rs530468819	in-del	-/A	0.0123207	0.0775148	intron-variant	EML5	GRCh38.p7	14:88649831	AATGTTTTATAGGGA[-/A]AAAAATACCTTAAAA	161436
rs530472571	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727762	GATAGGTTATTTCTA[C/G]CCTGACCAAAGGGAG	161436
rs530497548	snp	A/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88622815	AGAATCTTTTTTTTT[A/T]AAAAAGGCCCTGATA	161436
rs530566063	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709796	GAATAAATGCATGAA[C/T]TGCAGCATATACTTA	161436
rs530605566	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760511	ACCCTGTATTTTACA[C/T]CATTAACCTATGTAT	161436
rs530606618	snp	A/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88630270	CCCGGCCTCAGGTGA[A/T]CTGCCTGCCTTGGCC	161436
rs530608973	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662396	AGTAATCTGCCAACA[A/G]ACTTCTTAGGCATAT	161436
rs530622667	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88661312	CCCAGGCTGGCCTGA[A/T]ACGCCTGGCCTCAAG	161436
rs530639852	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766911	TGAGTATCGGGGGCT[A/G]GTTTCCCCCGATAGC	161436
rs530656199	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88713572	AGCCTTGAACTCCCA[G/T]CTCAAATGATCCTCC	161436
rs530657105	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733664	GACATATGACCTATG[C/T]CATCTCCCATCCCCC	161436
rs530668276	snp	G/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680396	TCTATCCTGGCCTGG[G/T]TTCTCCACAGAGAAG	161436
rs530678162	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88639906	TTTTTTGATCAAATA[A/T]GTATAATGTGATTCA	161436
rs530680745	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88668944	AAGAAGACCGAAAAC[A/G]GCAAGTGAATCCTGC	161436
rs530711137	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643094	TGTTTTGTTGTATAC[A/G]TAATACTAGTAGTGT	161436
rs530711407	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750403	TATTATTATTGCTAT[C/T]AGTTTACTATAACCA	161436
rs530722519	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653936	CTTTTTTTTGGTTGG[C/T]AGGCTATTAATTACT	161436
rs530737729	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613439	CACTATAAATTATAG[A/G]ACAAATGGGAAACAA	161436
rs530799192	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757167	TCCAGAAGTAAACCC[A/G]TACATTTGTGGTCAA	161436
rs530810240	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88712848	GTGGCAAATCAGGTA[A/T]TAAAAAAGAAGCCTA	161436
rs530821840	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768279	TTTTCTTTGTAGTCA[C/T]TAAGTATGCTAGGGG	161436
rs530823807	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615353	CCTTTAGGATGATCA[C/T]GACTTTCCCTTTCCT	161436
rs530844843	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720375	ATATCAATGCAAAAA[C/T]CCTCAGTAAAATACT	161436
rs530868367	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88764282	AGTTGAGAAGTAGTA[C/T]TTCCTCTTCTATTTT	161436
rs530892949	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88718353	TCTAGGGAGAAAACA[C/T]AGAGTAAAAAGAAGA	161436
rs530921389	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620767	ACCTGATATCATGGA[C/T]TGCACATCTCCTGTC	161436
rs530926725	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88717700	GCAGAGGTTGCAGTG[A/C]GCTGAGATCCTGCCA	161436
rs530927644	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726289	AAAATTTTAGCCATT[A/C]ATCTATTAAGCATTC	161436
rs530928104	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667626	CACAGACTTTTTTGC[C/T]AGCTTGCCAGTAGAG	161436
rs530950809	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88714644	GTATCTATCAAAACA[G/T]TACATTGTAAATTTT	161436
rs530959938	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88765017	CATGAATAATAAAGT[C/T]CTTTGTCTCTAACCT	161436
rs530963888	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88638033	GATATTAAAAGTATA[A/C]ATTATCTTAGTCAAG	161436
rs530965946	in-del	-/CT	0.0146672	0.084371	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768443	TGAGACAGAGTTTCG[-/CT]CTGTCACCCAGGCTG	161436
rs530973379	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710918	TTGTGCAATAATATC[A/G]ACTTCTCTCTTGCAA	161436
rs531018951	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748830	CAGCTCAGACAATGA[C/T]GAAAAGATAAATAAA	161436
rs531025155	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88648456	CCTCCCACGCTCCAG[A/G]CATCTTCCTGCCACA	161436
rs531027068	in-del	-/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88772283	ACTACTTCGGTAGCC[-/T]TCTGTCTACCTACCA	161436
rs531027302	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645345	TTTTAATTTCTTTGG[C/T]GTACGTGTCATAATG	161436
rs531099194	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740802	TCTGTAAGAATAAGG[A/G]GTTTGAATCAGATTA	161436
rs531114030	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690321	GGTTCATTCTGACTT[C/G]TGGATTGAGAATAGA	161436
rs531167244	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656598	TTCTGCACATGTATC[C/T]CAGAACTTAAAGTAT	161436
rs531233187	snp	C/G	0	0	intron-variant	EML5	GRCh38.p7	14:88703355	AGGGCAGAGGTGGGA[C/G]AAAGATTTTCAAACT	161436
rs531286399	snp	C/T	1.68866e-05	0.00290569	intron-variant	EML5	GRCh38.p7	14:88714932	ATAATTTGCTAGAAA[C/T]TGTTACCTGGCATTC	161436
rs531357770	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655710	CAGAATGGGAGAAAA[C/T]TTTTGCAATCTATCC	161436
rs531358416	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88643268	AATGGAATCACAAGG[C/T]AGTCTGATTCCAAGA	161436
rs531367136	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88737408	GGCTGAGCATGGATC[C/T]TGCAGCAAGTGTGGG	161436
rs531371532	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697078	ATTTATTAAATAAAA[A/G]TTTAAAGCAAACTAT	161436
rs531375270	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88733764	ATCTGGAAACAATTA[A/G]GTTGAGTCCCCATCT	161436
rs531417327	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706515	TGAACCACTGTATCA[C/T]CCTTCTATCTGAATT	161436
rs531431594	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617588	AGCCTGGGCAATATT[A/G]TGAGATCCCTATCTC	161436
rs531447953	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792114	CGGACCCGAGAGAGA[A/G]TCCCTAGACGAGGAA	161436
rs531474477	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88645234	TTTCGCCATGTTGGC[C/G]AGGCTGGTTTGGAAT	161436
rs531543428	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88669960	GAGGGACCCAGGCAA[A/C]GAAGGTCTGGAGTGG	161436
rs531550899	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88649824	TGTAGTTAAATGTTT[C/T]ATAGGGAAAAAATAC	161436
rs531564624	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693734	AGTATTATTCTCTTA[C/T]ACACTTCAGTTTCTA	161436
rs531586115	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88692192	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC	161436
rs531598808	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700530	AGGAATTCTTCCAAC[G/T]ACTTAACTTTATCTA	161436
rs531603345	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693345	CCTCACAATCATGGC[C/T]GAAGGTGAATGAGGA	161436
rs531624147	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88647235	CAGGCATGGTGGCAC[A/G]CACCTGTAATCCCAT	161436
rs531627865	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88636148	CAAGAGTATACACAT[G/T]GGTTGTACAGTCTGT	161436
rs531658848	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88698450	TTTTGTATTTTTTGT[A/G]AAGATGGGGTTTCAC	161436
rs531694369	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697977	CCCGACCTCAGGTGA[C/T]CTGCCTGCCTCGGCC	161436
rs531702922	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743607	AAAGAGGTTAAATAA[C/T]TCATAGCAGGTTAAA	161436
rs531712062	snp	C/G	0.000194502	0.00985968	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705529	CAATTTCAGAATCCA[C/G]TTCTGGAACATCAGA	161436
rs531717027	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684799	AATTTTTTCTGTATA[A/C]ATTAACAGAAAAAAA	161436
rs531718870	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88632793	ATTTTGGTAGTTAAG[C/G]CTGGTCTTTATCCCT	161436
rs531742446	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88654851	TTAATTTTCTGTCTC[A/G]TTGATCTAATATTGA	161436
rs531775494	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788734	AAAAATTTGCTTACG[C/G]GAAGTACCTAGAATA	161436
rs531783271	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88624276	GATGGGGTTTCACCA[A/T]GTTGCCCAGGCTGGT	161436
rs531799749	in-del	-/ACTT	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88618470	AAGATCACTACAAAA[-/ACTT]AATAGGAGAAAAGCT	161436
rs531824679	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678535	AGACAAAACTGGAAT[G/T]CATGAAGGGACATAC	161436
rs531872110	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88646389	CAAACCTTCTTCATA[C/T]ACTTTTTTGGATGCC	161436
rs531878768	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88771750	CCCTCCATTTTTCAG[C/T]AGTGTTTGACATAAC	161436
rs531885135	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685327	TAATCTCTAAATAAG[C/T]ACCACCTATGTCTTA	161436
rs531890215	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751397	AGATTAGAGAGATCA[C/T]GGTGCTTTCAAGAGA	161436
rs531917786	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789800	CCAACATTGCACTCA[C/T]ATTTTCAAAACCTGA	161436
rs531920670	in-del	-/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88680815	CAATCCAGACATCAT[-/G]GGATTCCCACAGGTA	161436
rs531931743	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774810	AATACTGTCTATATG[C/T]TGATAACATTCAAAT	161436
rs531940010	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88670562	CAGAACTGGGCAAAG[C/G]CTGAGATGGATGAAT	161436
rs531987949	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88619711	TTGAGACGAAGTCTC[C/G]CTCTTGTCTCCCAGG	161436
rs532003811	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677773	ACCAGTCAGAATGGC[A/G]ATTATTAAACAGTCA	161436
rs532008761	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88781791	CCCCTTCTGCCATAA[C/T]TGTAAGTTTCCTGAG	161436
rs532010717	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769924	AGAATTGGTAGCCCT[A/G]TGGAGGACAATTTTA	161436
rs532013960	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623868	GACGAAATAGAGCCC[A/G]TTTATGGATTTTATT	161436
rs532028333	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88672046	CAGCTCCGGATCAAG[C/T]GGACCTGATAGATAT	161436
rs532037790	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88622054	CCCTTGTCCGCCTCC[A/G]GTAACCACTATTCTA	161436
rs532071005	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88790221	ATTTGTGCCACCAAT[G/T]TCAAGATGCTGTATG	161436
rs532081465	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88694737	TTGTTATAGCTTAAG[A/G]TAGCCTTTCCAACTA	161436
rs532086117	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640775	AAAATAAAAAAATCG[A/G]TTTTTTGAAAAGATA	161436
rs532086393	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88631832	CAGGTGTGAGCTACT[A/G]CGCCCAGCTCATATC	161436
rs532120371	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740130	CAACAAGCTTTTTTT[A/C]AACACTACTCTTCAG	161436
rs532135735	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718648	AAGCTGAAAGCAGAA[G/T]GCATATAGGAATGAG	161436
rs532151782	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88644163	TTCTATAAGCAAAAG[A/C]TCATTCACACATACT	161436
rs532157176	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88739076	CATCTACTATATGAA[A/G]GTAGAAACCCTTTTA	161436
rs532161985	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88782124	TGTCTAAAATGATGA[G/T]AGTGATATGGACAAT	161436
rs532239766	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702291	TGTAGGAAAAAAGTT[A/T]GGGGTAAATTTTATT	161436
rs532277004	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673904	GAAATAATTCCATGC[G/T]CATACATAGGAAGAA	161436
rs532279194	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651701	AAATATTCTAATTAG[A/C]ATATTTAAATAATAT	161436
rs532283705	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88747204	ATTGCTTGAGGCCAG[A/G]AGATTGAGACCAGCC	161436
rs532298977	snp	C/T	0.00139343	0.0263586	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620869	CCACCATGTCCCCTT[C/T]AGGGCTGTAACACAC	161436
rs532302845	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755048	GACCTCAAGTGATCC[A/G]CCTGCCTCAGCTTCC	161436
rs532342172	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88667711	TGCTGTTTTACTAAC[A/T]GAGCCCGGGCACTGG	161436
rs532361654	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770074	CAGCAGCAGAGGAGA[A/G]GAAAGAGCGCTTGTG	161436
rs532379165	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771956	ATCCAATCCCACAGC[G/T]TTAAATGCATATAGA	161436
rs532400975	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776193	AATACCTAACTCTTC[A/G]ATGCCCAGACACCAA	161436
rs532413083	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672514	AGAGCAAACAAACCC[C/T]GAAGCTAGCAGAAGA	161436
rs532437955	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786045	CTCCAGCCACACTAA[C/T]ATTCTTACTATTCCT	161436
rs532455429	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88637839	AGAAGCTAGACCTAT[A/G]TATTTATATGCAAAG	161436
rs532472933	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680280	CCAAACAGCATATTG[C/T]CATTTTCTTCTAGTA	161436
rs532500909	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716076	AAGTAAAAATTCTTA[C/T]TTTCAATCAGTGTCA	161436
rs532506660	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626723	ATGCTTGACCAGGGC[A/G]TGTAATGATTAGCAG	161436
rs532513909	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635078	CCAAGAAAGAAAATG[C/T]GAAAGCTCATGCTCA	161436
rs532524805	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730780	CAATGCAACCTAAAT[G/T]GGAATCTGCTAAGAT	161436
rs532529310	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658986	TATATACCCATGTAA[A/G]TATCTTTCATCTCAA	161436
rs532548136	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88659143	CATCATAAAGCAGGT[C/T]TTCCGTTAACATCTT	161436
rs532562130	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88690095	AGCAAGTGCAAAGGC[A/C]CCGATACAACAACAT	161436
rs532579087	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88621033	GAATTCTGGCAGTTC[C/T]TTAAGTACTAGCAAT	161436
rs532587737	snp	C/G	0.000215415	0.010376	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658298	TATCTGTACCGCCTA[C/G]GGTAACCAACATGCT	161436
rs532626196	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731146	ACATATGTATACATG[C/T]GCCATGTTGGTGTGC	161436
rs532673243	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709430	TAACCCAACAGAAAA[C/T]AGGAAAGAGATATGA	161436
rs532704094	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666112	TGATGAAAAAGAATG[A/G]GAGATTTTAATTAAC	161436
rs532753569	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721178	TGAGTATCATGAAAA[C/T]TGCCATCCTGCCCAA	161436
rs532760173	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766935	CGATAGCACACAGTT[A/G]TAACAAATGTTTTAC	161436
rs532760542	snp	C/G	1.67795e-05	0.00289646	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661746	AAGAAGCAGTTACAT[C/G]TGTAACTTCTCCAAT	161436
rs532761665	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88623605	TTTTAGTAGAGATGG[A/G]GTTTCACCATATTGG	161436
rs532794187	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623717	GCAACTGGCCCAGAG[C/T]TTATTTTTGAAGGCC	161436
rs532794337	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88773595	GCCTGCATATTACAA[C/T]CATTTGGGAAGCTTA	161436
rs532795363	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668188	TAGCAATTCTTTTTA[C/T]TAAATTCCCACTGTT	161436
rs532799523	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677390	TTCAGGACACAGGTA[C/T]AGGCAAAGATTCAAT	161436
rs532830609	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773175	GTCTGCTGAAATCAT[C/T]ACCTGAGGCACTGGG	161436
rs532847263	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88619464	TCCCCCTTGGCCTCC[C/G]AAGGTACTGGGATTA	161436
rs532852329	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780614	TCTCACTCACTGTGT[C/T]ATCCAGGCTGGAGTG	161436
rs532871359	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630859	AGCCTTATCGGTGAA[A/G]CCAACACTGTGGATA	161436
rs532883947	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728650	AGAGGCTTGTCTTAC[A/G]ATCTCAGGGGTGGCA	161436
rs532925195	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655589	TTCATGACTAAAACA[C/T]TGACAGCAATTGCAA	161436
rs532962536	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752175	TTTCAACTAGTAAAA[G/T]CTATGGGCATGATTT	161436
rs532968185	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88704529	ACACAGAGAGGTTAA[G/T]TGACTTGTTTAAAGT	161436
rs532968613	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88677562	CTGTCCATCTGACAA[A/C]GGTCTAATATCCAGA	161436
rs533002546	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88639530	ATAATTTGGGCCATA[C/T]TGAGTCACATTTTAT	161436
rs533039426	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88623269	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	161436
rs533045379	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720465	TCCCCGAGATGCAAG[C/G]CTGGTTCAACCAATG	161436
rs533047663	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779859	ATTGTGAGTTCATAT[C/G]GACATTTCCAATTCA	161436
rs533082450	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727881	GACCACAATGCTAGA[A/C]ATCAACAACAAAAAA	161436
rs533095003	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616074	AAACCAAAGCTGTAG[G/T]AGTTGTTGTATTAAG	161436
rs533104592	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661552	ATTACAACATTACAT[A/G]TTACATATGTACAAT	161436
rs533134375	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88636534	GGCATGGTGGCGTGC[A/C]CCTGTAGTCCCAGCT	161436
rs533145990	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742786	AAAAATAAATATTTA[C/T]TACTATCCATCAATC	161436
rs533187581	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635211	TTGTTTTTTGCTTTG[A/G]TAAAGCTTTATATCC	161436
rs533208004	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760538	GTATCTATCCTTTCA[C/T]CAATACCACACTGCC	161436
rs533208508	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706187	GATTATACTTTAATA[A/T]AAAATTGTTATTTGG	161436
rs533222720	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88757288	CACATACAAAAAAAT[A/T]AATTTGGACACATAC	161436
rs533224018	in-del	-/CA	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88669519	CTGACCATAACCCCT[-/CA]CACTGTGCGGGGCCT	161436
rs533242984	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88667012	ATTTCAAAGATAGAG[C/T]TGGCAGAACTTTGAC	161436
rs533249128	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88743598	TAAAAGCTCAAAGAG[G/T]TTAAATAACTCATAG	161436
rs533255125	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693477	AACAGTATGGCGAAC[C/T]GCCCCCATGATTCAA	161436
rs533258502	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88774559	CAAAACTTCGCTAAG[G/T]TGAAGCAGTCCTCAT	161436
rs533266406	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711023	ATAGAGGTCAGTATG[C/T]GAAACAGTAAGTAGG	161436
rs533301791	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668288	ATGAAAAGAAAAGTC[C/G]GGGGAGAAGCGCTGG	161436
rs533338172	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88749079	AAATTTAAGACGTTC[A/T]ACAAATCCCAAGCAG	161436
rs533340086	in-del	-/AGAT	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612742	GATAGGTAAACTGCA[-/AGAT]AGATAGGATGAAACT	161436
rs533359090	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88714311	AAAGAGAATCTGTTT[G/T]AGATCCTCCAGCCAA	161436
rs533376800	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758204	TATGTGTATTTATTT[A/T]TTTTTGACACAGAGT	161436
rs533389360	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660438	ACATTAGCATAGGTA[C/T]GTAGAATGCCAAAGA	161436
rs533405734	snp	C/G/T	0.00239393	0.0345281	intron-variant	EML5	GRCh38.p7	14:88704317	TCCCCCTTTGCCTTC[C/G/T]GCCATGAGTAAAAGC	161436
rs533413061	snp	A/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791892	ACCGCTTGCTGTGCT[A/T]CCATCAGTCCTTTAT	161436
rs533428057	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697869	GCCTCCCAAGTAGCT[A/G]GGATTACAGGCATGT	161436
rs533430703	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638832	CCAGTTGCCACTATG[C/T]TGATAAATTTGGGGT	161436
rs533484465	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613681	GAAGGAAATGAGCAT[A/G]GTTGGCGATTGGAAG	161436
rs533493982	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740828	GATTATTTTTAAAAT[A/G]TGCTATGCTTTCCTT	161436
rs533495148	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750070	CACTGCAATGCAGAG[C/G]TGAGTAGTTATAGCA	161436
rs533503687	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88722917	AATAAAAATTAAAAT[-/A]AAAAAAAATGTTCAT	161436
rs533506545	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755950	GAACCCAGGAGTTCA[A/G]GGCTGCAATGAGCTA	161436
rs533506672	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633329	GTCTTGCTGTTGCCC[A/T]GGCTGGACTTGAACT	161436
rs533527023	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736835	CCTAATTTTTTTTTA[C/T]AGTGTTGTGCCCATC	161436
rs533550963	in-del	-/G	0.106987	0.205054	intron-variant	EML5	GRCh38.p7	14:88728211	AGACTTTTTTTTTTT[-/G]GTCATTATTCCCTAA	161436
rs533561876	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88736190	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTATGTT	161436
rs533577402	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88641571	AATTAAAAACAAAAA[A/C]CATATGATTATCTCA	161436
rs533609134	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88744340	TAACACCTCTGTTTA[C/T]TTTTAATTTTTAAAA	161436
rs533612146	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683751	ATAGACATAGAAAAA[A/G]CATTTGATGAAAATG	161436
rs533615638	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787911	TTGTGTTAAGAATTC[C/T]AGGCATGGTGGGGGC	161436
rs533642152	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88720112	GAATCCCTAAATAGA[A/C]CAATAACAAGTTCTA	161436
rs533711084	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618031	AAAAAACTTGATAAA[C/T]CATGGAAACTGATAA	161436
rs533721120	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88656394	ACACCACATGTTCTC[A/G]CTCATAAGTGGGAGT	161436
rs533726942	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88644720	TATTCATTTTATTTT[-/A]TTTTTTTTGAGACGG	161436
rs533733403	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769538	TTTAGAGAAAAGACA[A/G]TATCTAAAAGGGCTC	161436
rs533744019	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642583	GGTTATGGGAAAATA[A/G]AATTAAAGTTACAAA	161436
rs533761735	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769212	GGAGGTGGAGCCTGA[C/T]AGGAGATAACTGGAT	161436
rs533799804	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88685857	TATTTTTATTGTTCT[A/G]TTGTTACTTTTTATT	161436
rs533800456	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745028	AAAAACTCCATTGAC[A/T]GTGTCATATTTTGTA	161436
rs533818196	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88791262	CCGTATTTGAAATGC[C/G]CAATTTAAATCCTGT	161436
rs533820502	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775127	ACCCGGGTACTATGT[C/G]AAGGGCCTTAAGTGA	161436
rs533829951	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693379	AAGTCACGTCTTACA[C/T]GGTGACAGGCAAAAT	161436
rs533832192	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782246	CATTTTGCCCCTGCC[A/C]TAGAGATCTGTGGAA	161436
rs533869097	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88633200	AAAAACAAATACTTT[C/G]TTTTATTGCCATCAT	161436
rs533872248	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624917	ATAATTAACTGCAAA[C/T]CTCAGGTAGGTCACA	161436
rs533878305	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730276	TCACAATTTTTCCAA[C/T]TCACAGGAAAGCTCA	161436
rs533920807	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669867	TCAGTGACCCTCTGG[A/G]ACAGAGATCCCAGGG	161436
rs533947588	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88729154	TCTGTGTGTGTGTAC[A/G]TGTACATATATATAC	161436
rs533967901	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672582	TAGAGACACGAAAAG[C/T]GCGTCAAAAAATATT	161436
rs533972577	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88773871	TGCCTGTGATCCTAG[A/C]ATTTTGGGAGGCCAA	161436
rs533986065	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684826	AAAACAAATTTTTTC[C/T]GTATACATTAATTTT	161436
rs534028683	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775679	ACCCACCCAAGCCTG[A/G]GGGAACTCACAGCGC	161436
rs534038752	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788805	GCTCACATCTGTAAT[C/T]CCAACACTTTGGGAG	161436
rs534045275	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684264	CAAGCTCCGCCTCCC[C/G]GGTTCACGCCATTCT	161436
rs534084744	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706769	AACTAGACCTTACCC[C/T]CATTATTCTCAACCC	161436
rs534096357	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686461	CTGGGCCCACAGCCC[A/G]GAGGATGGTCGGCGG	161436
rs534123933	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752341	CACCTTAAATAAGTG[G/T]TTTTTAAAAATAACT	161436
rs534128319	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88622048	CCCTCCCCCTTGTCC[A/G]CCTCCAGTAACCACT	161436
rs534214900	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714399	GGTAGAGGTTGGTGG[A/G]GGCCGGGGTGGATAT	161436
rs534220826	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705985	TACCCATCTCTCAGA[A/G]GATATATTAAATGTT	161436
rs534240089	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88669315	CGGCTGTCATCACTT[C/T]GGCTGTCTGCTGCCT	161436
rs534255063	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677169	CTTGGCCTCCCATAG[C/T]GCTAGGATTACAGGA	161436
rs534257855	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88621476	CTACAGGCACACATC[C/T]ATCTGTAAGCACAAT	161436
rs534272275	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631996	TACTTCCTTATTTTT[A/C]CATCCCCAAATCTAC	161436
rs534277214	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790975	TTTCAAAGTAATACA[C/T]TAAATACAATCTGAA	161436
rs534282161	in-del	-/GTTC	0.0193772	0.0965046	intron-variant	EML5	GRCh38.p7	14:88760349	AGGTTATAGTTGTTT[-/GTTC]GTTTGTTTGTTTTTT	161436
rs534322672	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88762301	GGATCACCTGAGGTC[A/G]GGAGTTCGAGACTAG	161436
rs534331049	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88669494	GCCAGACTGCCTCTT[C/T]AGGTCGGACCCTGAC	161436
rs534335406	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735416	ATAGGCAAACAGCTT[C/G]AACAGGTCAAAGAAA	161436
rs534358610	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674128	ACAAAAATTAGCCAG[A/G]CATGGTAGCGCATGT	161436
rs534367212	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673199	CACCACGATCAAGCT[A/G]TCTTCATCCCCAGGA	161436
rs534390376	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655813	AAAAAGCTAAGGATA[C/T]GAACAGACACTTCTC	161436
rs534410389	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717331	AACAAGGGGACTTTG[G/T]TGTGAACTCAGTCTG	161436
rs534424457	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785521	GAGCTGTTGATCTTT[C/T]CTTCTGTCCAAAATA	161436
rs534426806	snp	A/G	0.00676609	0.0577691	intron-variant	EML5	GRCh38.p7	14:88681454	TCTCTCTACCCTGAC[A/G]GCTTCATCTGCTTCC	161436
rs534436702	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88645888	TCTATTTATAATGTG[C/T]CGTGTCCCAACAGGT	161436
rs534459638	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615057	CACCATTGGGAATGA[C/T]TGTTCATCATACTAC	161436
rs534460151	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767565	ATAATATTGTTACAC[C/T]GTAAGAGTTCTTAAT	161436
rs534460176	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662824	GTTGGGATTACAGGC[A/G]TGAGCCACCATGCCC	161436
rs534462946	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88760799	TAAACATAGTACGCC[C/T]GCCCTCCATTTTTCA	161436
rs534470555	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703761	CTAAGAGAATCCAGA[A/T]CCCGTATTTTGGTGA	161436
rs534492839	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731520	TGTGAATAGTGCCAC[A/T]ATAAACATACGTGTG	161436
rs534523194	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660138	TTTTTTTTACATTAG[C/T]CAGGCATGGTGGCAT	161436
rs534534427	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88697791	CCCAGGCTGGAGTGC[A/G]ATGGCGCTATCTCGG	161436
rs534538420	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88747523	TCACAACAAACAGCA[A/C]AGTCGGCCTTGCAAA	161436
rs534540213	in-del	-/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88648388	GACAGGGTCTTGCTC[-/T]TGTCACCCAAGCTAG	161436
rs534601866	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613700	GGCGATTGGAAGCAA[C/G]GGTACCAGAGGGCAC	161436
rs534618628	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725968	CTGAGGTAGAGAAGA[A/C]AGACTTCGTAAGTAC	161436
rs534635325	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710302	CTTTGAGCTAACTTC[A/G]TATATTTTTTGTTTC	161436
rs534688080	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88650394	AGGAGTTGGAGGTTG[C/T]AGTGAGCCAAAATCG	161436
rs534728148	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88754864	GCTGGAGTGCAGTGG[G/T]GTGATCTCAGCTCAC	161436
rs534758802	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88657260	GAGGTGCTGTGAATT[G/T]TCTATAGCAAGAATA	161436
rs534759531	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627301	AGGTAATATTATCCT[A/G]CTGATCTGCCATTAT	161436
rs534771544	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744780	TGCTTTCTGGTAGTC[A/G]TCATGTTTCTTTGAC	161436
rs534771836	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88775904	GCTTTAGGTGGCTCA[C/G]AAGAGAGAGAGAGAG	161436
rs534796129	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88618980	GATTGTCTGGGTTAC[A/G]TGAAATAAGGAAGCT	161436
rs534799126	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645033	TTTTCTCTTCTTTCT[C/T]TCTTTCTTTTTTAGA	161436
rs534801012	in-del	-/A/AA			intron-variant	EML5	GRCh38.p7	14:88734011	CAACCTACACGAAGT[-/A/AA]AAAAAAAAAAGCAAG	161436
rs534830805	snp	A/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648872	TCATACTCTGAACTC[A/G/T]TATCTTTGTACACAC	161436
rs534847042	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88679072	CTGCTTCCATCATCA[C/T]GCTGCATTCTCCCAG	161436
rs534868354	snp	A/T	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614697	TTCCTGAATGATGAG[A/T]AGTGATCTTTGGCAG	161436
rs534887005	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88659517	GCGCCCAGCAGGAAT[A/G]ATGACTCTTAATAAT	161436
rs534904358	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748499	TGAAAGCAAGCTTTT[C/T]ACAAAGATGAAACTG	161436
rs534920705	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635534	CGGCCTAAATATTTT[A/G]AAGCTATCCATCAAG	161436
rs534931642	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88784730	GCAGTAACAAATGCT[A/G]GAAAGGATGTGGAGA	161436
rs534959461	snp	C/T	3.64199e-05	0.00426716	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712463	CTTTTATTTCTTCTG[C/T]ACTTGTCACTTCCTT	161436
rs534992733	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88687942	GGGTGTGGGTGGCAC[C/T]TGCCTGTAGTCACAG	161436
rs535006355	snp	A/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	EML5	GRCh38.p7	14:88792650	CAGGTGCATCTCGTT[A/T]CGGGGGCCGCCGCCG	161436
rs535008281	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88753750	ATCCTTTGTTGTGAA[C/T]TTTGATTTTGTATAA	161436
rs535029714	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694107	ACCATAGACCATTTG[C/T]TGAAACTAAGAAACC	161436
rs535033709	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88643759	ATAAAAACTAAGTAT[A/G]CTGTCTCTGACAATT	161436
rs535075644	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646735	TTATACAAGTTGAAT[A/G]GATAAGTTTTAGTAA	161436
rs535082523	snp	A/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618712	TTGGAATGTCTTTGC[A/G]GTAGCTGATTCTGTT	161436
rs535085717	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665612	CAGGAGGACTGCCCG[C/T]GGCCAGGAGGTTAAG	161436
rs535087112	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654159	TTATTGTGTCTTTTT[G/T]ATTTTTCTCTCTTTT	161436
rs535120816	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88708779	AGTTTTAAATGTAAA[C/T]TGGATTATATGCTCA	161436
rs535138711	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759797	AAGTTAGAGAAAAAG[A/G]ATAGGGTGGGTCCGT	161436
rs535146747	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653615	ATTGATTTTGGTATG[C/T]TGAATGAGCTTTGCA	161436
rs535151347	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88716278	AAGATAAATCCAAGA[C/T]TGTATTATTTGAAGC	161436
rs535171633	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636463	GTCAAGAGATCAAGA[C/G]CATCCTGGCCAACAT	161436
rs535187407	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615464	AAAAAGATAATGAAA[A/G]TTATCCAAATTGGGT	161436
rs535198230	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731338	GGTTTTTGTCCTTGC[A/G]ATAGTTTGCTGAGAA	161436
rs535209858	in-del	-/ATT	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88693090	ATACACTTTTGTATC[-/ATT]TAATAGCATATGAGT	161436
rs535215901	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88667400	AAATTTGAGAATAGC[A/G]TAGGTCTTCTCTCTT	161436
rs535236329	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88738526	CCTCAATATTTACCC[A/C]CAACTGTTTATTTAG	161436
rs535305488	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88640425	CACAATTACGTAAAA[A/G]TTAAATAACTTGCTC	161436
rs535315927	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684946	CATCACTGTCAACTT[C/T]TGGCTCTTATATATT	161436
rs535339534	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88782887	GAGTTCAAGATCAGC[C/T]GGGCCAACATGGTGA	161436
rs535342616	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735495	AAATACATATTTTCA[A/G]ATATAACAAGGTATC	161436
rs535373710	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88691671	AGGCAAGAAGCCCCA[C/T]GTTAACCTCAAGCCT	161436
rs535374554	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765768	TTATTTATATTTTTA[C/T]ATTTTCAGTTCTAAG	161436
rs535381591	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788253	ATTTTGACTTGCGTT[C/G]AATAAATTAAGTTTC	161436
rs535387246	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647384	AAAAAAAGAAAAAAA[A/G]GAAAGAAAAAAGAAT	161436
rs535455388	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750850	TCTAGCTAGAACAAA[C/T]GTATCTACCTCTTGC	161436
rs535459684	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88733078	TGCTATTTGAATAAC[A/T]ATATCAAGCTGCTTT	161436
rs535493407	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695028	ATCTTTTTTCACTTT[A/G]ATATATAATATAAGC	161436
rs535525292	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778684	CTCAGGAGGCTGAGG[A/C]AGAGGAATCACTTAA	161436
rs535604272	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736081	TCTTGGCGCACTGCA[A/G]CCTTCGCCTCCTGGG	161436
rs535627978	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614974	AATGTGTATATATTA[G/T]ACTACATTAAATATG	161436
rs535627984	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623362	AAAAACAATTTTATT[A/C]AAAGGATAATGGAAA	161436
rs535629064	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88720546	TGATTATCTTAATAG[A/G]TGCAGAAAACGCCTT	161436
rs535649842	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669071	CACCTGGGAGCTGCA[C/G]AGGACAAGGGGAGCT	161436
rs535688567	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766165	CCCTGTGATTATTGC[A/G]TTAACTGCACAAATT	161436
rs535697145	in-del	-/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88623431	GAGTTGATTTATTTA[-/T]TTTTTTTGAGACAGA	161436
rs535706900	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773262	TTCCCTGTGAGTGAG[C/G]ATTTTTCTGGACTGA	161436
rs535733433	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622910	AGTCAAAATAAACAT[A/C]CAGTTTCAGTGAATT	161436
rs535737759	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88734013	AACCTACACGAAGTA[A/C]AAAAAAAAGCAAGTA	161436
rs535765271	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691084	TAGAGACTCTGCTAA[C/T]GGCAACTGCTGGGTA	161436
rs535773507	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698634	TACAAACCTCTCCCA[A/C]GGTGGTCTTTAATTC	161436
rs535774711	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727365	ACCATCTCTTTCCCA[A/G]CTTCTCAACTCTGCA	161436
rs535776361	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88777440	TGCTAAAGGAAGCAC[G/T]TCAATCAGAAAGAAA	161436
rs535790056	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734978	GAGACAATCAGGAAT[G/T]TCTATACTAGCTAGA	161436
rs535795115	snp	A/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622358	TACTAGAGTTGTTAA[A/T]TTGGCAGATTCTAGA	161436
rs535809652	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730919	TTGTATTATTCTTTA[C/G]CACGTACTTAGTGAA	161436
rs535811861	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630493	ATTCAGGAATCTACT[A/C]CTTCCTAGAGCGTAA	161436
rs535847272	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730461	TTTTGAATTGCAGCA[A/G]CTTAAGAAATATGTC	161436
rs535865222	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88645920	TATTGAGTTCACATT[C/T]TGAATTACTTAAATG	161436
rs535876712	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88683057	CTCATGCATAAGTAC[A/G]TCTCAAAAACAGTGA	161436
rs535896658	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787363	GCTCAACAAATATTT[C/T]TTGGATGAGAAAACT	161436
rs535928147	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88733014	TAAGGCAAAAGCAGC[A/C]CAATGTAATGTGAAA	161436
rs535929805	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88689775	AAGAAAAAAGAAATA[A/T]ACATGCCAGGCACTA	161436
rs535937196	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786625	GTGTTGTGGGAGGGA[A/C]CCAGTGGGAGATAAT	161436
rs535957490	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752497	TTTGTGCAATTGCCA[A/G]ACACTGCTATATGGT	161436
rs535969437	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88696589	AATTTAGGTTGTTAC[A/G]TAGATAAACATTTTT	161436
rs535970895	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88755550	AGTTTATGTACATCA[C/G]CAGAAGGCGGGGAAA	161436
rs535971698	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88701518	TTTTGAGTGAATGAA[A/G]GAAAGGAAGAAGGAG	161436
rs535998387	snp	A/G	0.000233166	0.0107948	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712371	TACTGAATTTATATC[A/G]TTGATATCTGAATAC	161436
rs536004115	snp	C/T	0	0	intron-variant	EML5	GRCh38.p7	14:88737009	TACCTGACTTCACCC[C/T]ATCTCGGGTACCCTC	161436
rs536011229	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708848	GATTCAGTAATAAGA[A/T]TAGTTAAGGCCTAAA	161436
rs536012793	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619823	GCGCCTGCCACCACG[C/T]CCGGCTGATTTTTGT	161436
rs536042798	in-del	-/A	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88655706	CCTACAGAATGGGAG[-/A]AAATTTTTGCAATCT	161436
rs536084760	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668445	TTCAGAAAAAAAAAA[C/G]GGAATGATAAATTGT	161436
rs536093935	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763418	AGAAGAACTGGATAA[A/C]TTTCTAGACACACAC	161436
rs536126051	snp	A/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619153	GGCAGATCACCTGAG[A/G/T]TCGAGAGTTTGAGAC	161436
rs536138596	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719954	CAAATGATAAAGGGG[A/G]TATCACCATTGACCC	161436
rs536149471	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88716437	TTAAATCCATATACC[A/G]TATTGCCCTTTGCTC	161436
rs536154720	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779279	GCCATAAAGAAAAAG[A/C]GAAACTATGAGTATC	161436
rs536170286	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683823	AAACTTAGTAAGGAG[A/C]ATCTACGAAAAACCC	161436
rs536171045	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88724188	GCTGAGGCAGGAGAA[C/T]CGCTTGAACCTGGGA	161436
rs536172119	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88675458	GCCCCTTTTAGCTAT[C/G]GATGGAGCTGCTGGA	161436
rs536204861	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714514	TTACTGTATGATATA[A/C]CTGAAATTTGCTAAG	161436
rs536229352	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619056	CAATTCCTTTAAAAA[C/T]GTCTAATGGCTTAAA	161436
rs536229521	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663616	TATGTTATATGATTA[C/T]GACTCTTTTTGAAGA	161436
rs536230701	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680761	ATTGTTTTTCAAAAA[A/C]AAGTCCTCGATCCAG	161436
rs536246924	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737617	AAGTTAATTTTGTAC[A/C]TTTTATATCTTAGAT	161436
rs536271469	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88710295	ATTCTCTCTTTGAGC[C/T]AACTTCGTATATTTT	161436
rs536284490	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767746	CTTATAAAAATGTTA[C/T]GAAATAGTACAGTTT	161436
rs536294926	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783726	GCTGGAGATTTCAAC[A/G]ACCCATTTGCAGCAC	161436
rs536295756	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687488	TTGTGTTTTTAAACC[A/G]TCTACATGGAATCTG	161436
rs536319082	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774346	AATAACCAAGTAAAG[C/G]AGAAACTGCTGGAAC	161436
rs536325529	in-del	-/CT	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88619788	TCCTGTTTCAGCCCC[-/CT]GAGTAGCTGGGATTA	161436
rs536402675	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88717225	AGGTAAAGGACCTGT[G/T]TCAGCAGAGACAACA	161436
rs536413077	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88719559	ATGGGTGCCTCTGAG[A/G]AGTTTGCTGTTGATA	161436
rs536420462	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88685601	ATTTGCATATAACCC[A/G]CATACATCATTCCAT	161436
rs536428747	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666289	TGGAGTGCAATGGCA[C/T]GATCTCAGCTCACTG	161436
rs536486226	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700140	GAATTAAACAAAATT[C/T]CCAAATTATAGTACA	161436
rs536522657	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88776603	ACAATGAAGTGGGTC[A/G]GGCATGGTGGCTCAC	161436
rs536523426	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88699472	TTTTTATCTCTTATC[A/G]TTTATAGCTTGTGGC	161436
rs536559669	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775767	CTTGAGCAAACATAG[G/T]CAGTAACCAGGGACT	161436
rs536559932	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88706913	AATGCAAGTTTGGTT[C/T]GACATTAAAAAGTCA	161436
rs536593183	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88655386	ATGAGAAAGGATTCC[C/G]TCTTTAATAAATGGT	161436
rs536627802	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659365	ACAGGGACCCGCCAC[C/T]GTGCCCAGCTAATTT	161436
rs536632582	snp	C/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765940	AACATAAATTGTGAA[C/G]ATTTCATGGACATTT	161436
rs536647522	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88707754	TAAATTTTTTATGTA[A/G]CTTAATATAAGTCAC	161436
rs536647586	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761711	CTTTGGGTATATACC[C/T]AGTAATGGGATTCTT	161436
rs536658204	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88636818	CACAGACAGATTTCT[A/G]TTGTATATGAAGAAC	161436
rs536658796	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667884	CAGTTCAATGATTTT[G/T]CCCTAGGTTAAGCTC	161436
rs536717418	in-del	-/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88634171	GTTCTCATGAGATCT[-/G]CTCGTTTAAACGTGT	161436
rs536721074	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667117	AAACTAGAGGAGGAA[C/T]CACCAGTGCTTAGTT	161436
rs536723966	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767285	AAACTTGGATGATTG[G/T]AGGTCAGTTCTCAAA	161436
rs536728860	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616491	AATTTGATAACTGAT[G/T]ATAGGTTTGGTGAAA	161436
rs536736954	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722282	TATACACAAAGAAAT[A/C]TAAATCATTCTATTA	161436
rs536739395	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714078	CCTGGGCTCAAGCTG[C/T]CGGTCCACTGTGGCC	161436
rs536750060	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88771472	TTTCTGGAATTATTG[C/T]TTCCTCACTACTGAG	161436
rs536753022	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778214	AAAATAAGACCTGAA[C/T]GAAAGAAGGAAAAAA	161436
rs536761812	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774043	ATAATCGCTCGAACC[C/T]GGAGGCAAAGGTTGC	161436
rs536764098	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88776863	TCCAGCATGGGTGAC[A/G]GAGCAAGACCCCGTC	161436
rs536767028	snp	C/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88786399	CAATTTTATCTGTTT[C/G]GTTCACTGCCATATC	161436
rs536787991	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629237	TAGATTTTCAAGAAA[C/T]ATCACTAACTTTGCC	161436
rs536793479	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633117	CCCTGAAACTGGTCT[G/T]AGCCTGCAGCCCCCA	161436
rs536833599	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88649403	CCATTTCCACACTGT[C/T]GTTTCAGAAACTCTT	161436
rs536843850	in-del	-/AGA	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88684731	TGGCAATTATTCCAT[-/AGA]AGAATATGTATATTT	161436
rs536859986	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88753761	TGAACTTTGATTTTG[C/T]ATAAAAAATAACTCA	161436
rs536885243	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88697554	TCACTTATTTTTTAA[C/G]TTGGTTTATGATGTT	161436
rs536908227	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762266	CTGTAATCCCAGCAC[C/T]TTGGGAGGCCGAGGC	161436
rs536914788	snp	A/C	1.67829e-05	0.00289675	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664495	TTTAAAGTCTTACCT[A/C]TAATATCCCAATCAA	161436
rs536923030	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704628	GTTGTCCCAACAATG[C/T]CCTTTATAATCATCT	161436
rs536926792	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696713	TATTTGATAAGGATA[A/T]CAGTATACACATTTG	161436
rs536936037	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762228	AACTTACAAAGACAC[A/G]GGCCATGCGTAGTGG	161436
rs536966584	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88715349	ATTAATTCAGCAACA[A/G]TACGTTGCTGAACAG	161436
rs536975393	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744453	GATTCAGAATGGAAC[A/G]TGACACTTACACAGC	161436
rs536993052	in-del	-/AGA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88749633	GATAGCACCATAAAC[-/AGA]AGAAAGGAAACAGCA	161436
rs536999939	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793808	GTACTTCGATTTTTT[A/T]AAAAATGACTGGGAC	161436
rs537016276	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674625	AAACCACATCATTCT[A/G]ACCCTGGCACTTCCC	161436
rs537019545	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88709970	TATTTTCTCCAAATA[C/T]AAATTTTCATTTGTC	161436
rs537027586	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738661	ATAATAGATATTAGA[C/T]TTATGAAAGAATCTT	161436
rs537032810	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88757817	CCTTCCTTCCTTTTC[C/T]TGCTTTCTTCCTTTC	161436
rs537035260	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88653164	TCCTGAGACTTTGCT[C/G]AACTTGCTTATCAGC	161436
rs537047682	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660165	GCATGTGCCTGTGGT[C/T]CCAGTTACTCAAGAG	161436
rs537050973	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88679397	TATAGCTTGCTATCA[A/G]TAAAGGGGCTATAGC	161436
rs537099791	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88681703	GCATGATGATAGGAG[A/G]TCCCATAAAGCCAAG	161436
rs537165164	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705834	CCCAATGACCGCTAC[A/G]TCAAATTTAAATGTC	161436
rs537169143	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726719	AAAAGGTTAGCTAAT[A/G]CATACTTTAGTAAAA	161436
rs537188095	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641503	ATCATTCCTGGCATG[C/T]AAGGTTGGTTCAACA	161436
rs537190297	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88682065	ATCAATTTAGTGTAT[A/G]TGTGTGTATATTTAT	161436
rs537195464	snp	A/G	1.65644e-05	0.00287783	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621288	GCATTCCTTGTCCCA[A/G]CAAGGATCTTGCCCT	161436
rs537197718	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88770544	GGAAAAAAGAGTGGG[A/T]TCCAGTACACAAGCA	161436
rs537213295	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732835	GTCTTTCTTTTGAGA[C/T]GGAGTCTGGCTGTTT	161436
rs537234409	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645969	ACCTTTAATTTTTTT[A/T]AAAAATGCAATTTAG	161436
rs537263418	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637296	CTCTGTACTCCCCAG[A/C]TTTTGACTTGGAAAG	161436
rs537264661	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645533	CCTTCTTGAAAGTGA[A/T]TTTTCGTAATATTTC	161436
rs537288560	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777643	ACAACTTTTTAAGAC[A/T]TACGCAGTACAATAA	161436
rs537292907	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88748297	AGCTAAAAGCAAAAA[A/G]TTCTCAGAGATCACA	161436
rs537293202	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758597	TAAAATGATGTAGCC[G/T]CTTTGGAAAACCGCT	161436
rs537304767	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774141	CAAAAAACAGAAAAC[A/G]AAAAACAAAAAACAA	161436
rs537327561	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785721	TTTGCTCTTTTGTCA[C/G]TACTTTCACTGTTAC	161436
rs537334503	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772967	ACTTGCTCAGAGAAG[C/T]TCTCCCTAACTACTC	161436
rs537345818	snp	A/G	0.000132494	0.00813815	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688461	TAGCCTTTTCTTCCA[A/G]TCAATCCTCCCCCTA	161436
rs537369578	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703851	TAGACATATTGAGGG[A/G]AGATGATTATCTCTT	161436
rs537376684	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644956	ACCTCAGGTGATCGG[A/C]CCGCCTGGGCCTCCC	161436
rs537378659	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636578	AGACAGGAGAATGGC[A/G]TGAACCCGGGAGGTG	161436
rs537381931	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88706726	GGCCTGAGGCCTTTG[C/G]GCTTAAGTGAAATTC	161436
rs537460541	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752298	AATGTTATAGATGCT[C/T]ATAATTAAAATGGCT	161436
rs537482638	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694976	AAATATAAGAAAATA[A/C]AAACCTATAACTTCT	161436
rs537516939	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658720	CTATGCTAAGAAATG[C/T]TATCTGTGTAAAAAA	161436
rs537544225	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88691922	AAAGTTATTCATTTG[C/G]AAGTATTTTCACTGC	161436
rs537563073	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705762	ACTGTACTACAGATT[A/G]TCTTCCTCTCCACTC	161436
rs537576936	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88655313	GAACAGAGGCCTCAG[A/G]AATAATGCCACATAT	161436
rs537584010	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88694692	CTATTTGTGGCATGA[A/G]TGGGTTAAAGTCAAT	161436
rs537606271	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628312	TCTCAAAAGAAATTT[C/T]CAACCATACAGATAG	161436
rs537617790	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622498	AAGCAAATCCATCGT[C/T]ATGCATTATTAAGTA	161436
rs537698727	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682202	AAACACAATAAAATA[C/T]CTCTGTAACAACTTT	161436
rs537702665	snp	C/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613932	GCTGATGACTACTTA[C/G]TCAATATGACCTTTA	161436
rs537713199	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689110	ATAACTATACCATGG[C/T]TTATCCATTTTCCTA	161436
rs537726150	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782193	ACTTGTTGGGAACTG[C/G]AGTAAAGATCAATCT	161436
rs537730486	in-del	-/TTTG	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88779622	TTGCCTCCTTGGAAC[-/TTTG]TTTGTCACCCTACTA	161436
rs537730664	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633234	ATTTATTGTTTTTAA[C/T]ACATTTCTTGCCATC	161436
rs537764302	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794552	TGTCACCAGGAGGGC[A/G]TTTTCTGTTTTTTAA	161436
rs537769686	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88791437	GCAATAATCAGTGGC[C/T]TAGAATGATTTCTGA	161436
rs537799829	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88736150	GGATTACAGGTGCCC[A/G]CCACCATGCCCAGCT	161436
rs537799990	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88628948	TATAATAAAATAGGT[G/T]ATTTATGTTTGTAAA	161436
rs537806090	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631175	AAAAGATATTCCCAT[A/G]GTGTCCACTGAAAAC	161436
rs537812843	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728253	TAACAACTATTTACA[C/T]GGCACTTACACTGTA	161436
rs537834516	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674161	GTAATCTCAGCTACT[C/T]AGGAGGCTGAGGCAG	161436
rs537835512	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735567	GTGAGAAAACAGGCA[A/C]TGGTAATATATTCAC	161436
rs537836541	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676955	TGTCTCCCAGACTGA[C/T]GTGCAGTGGCACAAT	161436
rs537877860	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88773392	ACAGGGAATATCCAG[C/T]GTGGGAGGGCCTTAG	161436
rs537882127	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691779	TACTTATTTCCCAAG[C/T]GGTTAATGAACTCTG	161436
rs537900203	snp	A/G	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684240	GGAAGTTAAAAACTC[A/G]GCTCACTGCAAGCTC	161436
rs537913907	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690984	GACCAAGTCTGTTTA[C/T]TTCTCTGCACCCAGG	161436
rs537932960	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788222	AATGTTATTCTGAAT[C/T]GCTTTTCCAATTACA	161436
rs537947651	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88733416	GCTTTTAAGGTGATT[C/G]ACATTTTAACTAATA	161436
rs537952925	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88690435	ATCATAGAAGATGAC[A/G]AAAAGTGGTTAGATT	161436
rs537985646	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88626072	CCTCCTTCTTCCCTC[A/G]AAGTAGAGACACTGG	161436
rs537985745	in-del	-/GTGAT	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88731819	TTTCTCTGATGGCCA[-/GTGAT]GATGAGCATTTTTTC	161436
rs538021093	snp	A/G	9.95917e-05	0.00705591	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616212	TATTTGTCACATGGG[A/G]CGAATGACCCAAGAA	161436
rs538042777	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760752	ACTTTGAAGAGAAGT[A/G]ACATCTTAATTATAT	161436
rs538083129	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767043	TTAGTAATTTTTATA[C/T]GCTAATTTTCAGTTA	161436
rs538087359	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782842	CCCAGCACTTTGGGA[A/G]GCTGAGGTGGGTGGA	161436
rs538096331	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685750	CCACCACAGCCGGCC[C/T]CCATGTGCTTTAAAT	161436
rs538138390	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721515	AAAACAAGCAAGGGG[A/G]AAAGGATCTCCTATT	161436
rs538162618	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88684960	TTTGGCTCTTATATA[C/T]TGAAATAATCAATTG	161436
rs538173613	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720565	AGAAAACGCCTTTGA[A/T]AAAATTCAGCATCCT	161436
rs538196237	in-del	-/A	0.386504	0.209444	intron-variant	EML5	GRCh38.p7	14:88738417	TTTAATCCCCAAGAG[-/A]AAAAAAAAAAAATCC	161436
rs538196386	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88622995	TACAATACATTACAA[A/T]ACATTATCCTCTCTC	161436
rs538201117	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623459	AGAGTGTCGCTCTGT[C/T]ACCTGGCCTGGAGTG	161436
rs538256420	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88630537	AACAAACTGCATGCT[C/T]AACTAATAAGTCTGA	161436
rs538267866	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88724222	GGAGGCTGCAGTGAG[C/T]CGAGATTGCGCCACT	161436
rs538286668	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676474	CCCCCATGATTCAAT[C/T]ACCTCCCACCAGGTC	161436
rs538297145	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683876	GTGGAAGACTAGATG[C/T]TTTCACTCTAAGATC	161436
rs538322329	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779435	TATCAACAGTTTATA[C/T]AATAAAGGCTAACAA	161436
rs538329765	snp	A/C			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765558	TTTAAGGGCTCACAT[A/C]ATTAGACTGGGCCCA	161436
rs538370254	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783858	ATGGCTACAGAATGC[A/T]CATTTTTTTCCTCAG	161436
rs538371411	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88639142	AGATTCCAAGTGCCA[A/C]AAGAGAGTTGGGATC	161436
rs538374355	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748971	ACAGGTAATCATGGC[C/T]CTAGAAGGAGAGAAA	161436
rs538389065	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88705297	GCATACTTAATATAC[C/T]AAGCATTTAATATAA	161436
rs538403251	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730955	AAATAAGACTCTCTC[A/G]TTTTTTTTAACCAAT	161436
rs538438799	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88662726	TTTTTGTATTTTTTT[G/T]TAGAGATGGGGTTTC	161436
rs538452887	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88661956	GTTTTAATGAAAAAA[C/T]AGTTAAATTATTAGT	161436
rs538454338	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88651360	AATATACAAGCTAAC[A/G]TCAAAGATTTCAGTT	161436
rs538503749	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773753	ATTAAGCAGCCAGGG[A/T]TGAGAATCAGGAATC	161436
rs538606137	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627180	CCCCTGCTCTACTAC[C/T]TAGCAATACATGATT	161436
rs538612878	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673129	AAGAATATTGATGCA[A/C]AAGTCCTCAATAAAA	161436
rs538625660	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88649420	TTTCAGAAACTCTTT[C/G]AAGACATTTTCACAT	161436
rs538641319	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731283	GTCCAAGTGTTCTCA[A/T]TTTTCAATTCCCACC	161436
rs538641955	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88657123	CTCAGCCTTTGAAGT[A/G]GCTGGGGCTACAAAC	161436
rs538660790	snp	C/G/T	0.000149798	0.00865321	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664534	ATGTAACTGGTAGCT[C/G/T]CTTTGCATATTCCTA	161436
rs538666523	snp	C/T			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615332	TTGCCTTTTAAAAAC[C/T]GTGATCCTTTAGGAT	161436
rs538705187	in-del	-/AA	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88671048	AATTCAAATTCAGGC[-/AA]TCCAGAGAACCCCAG	161436
rs538710864	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768645	TCGAACTCCTGACCT[C/T]AGGTGACCCACCCGC	161436
rs538713631	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775877	ACAGGGTGATTATGT[A/C]ATTCACCCCCAGCTT	161436
rs538717430	snp	C/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626544	ATCACTTGAACCTGG[C/G]AGATGGAGGCTACAG	161436
rs538754251	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767823	AACCATATAGTAATC[A/G]GGAAGAAGAAGGAAA	161436
rs538754339	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775061	TACTCCTGGCAGCAT[C/T]CACCACCTGCTAACT	161436
rs538761914	snp	C/G	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88617422	AAAGTGCTGGGATTA[C/G]AGGCTGAGCCACCGC	161436
rs538784101	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635457	GGTCTGGAGAGACTA[C/G]GTTTGTCTCTGAATA	161436
rs538785376	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88752047	CCTTTAGCTATTATG[C/T]TTTTATGAACTTAAA	161436
rs538843834	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658873	ATGTACTGTTGGAAA[C/T]AGATACAATAATTGA	161436
rs538873569	in-del	-/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88743009	CCAATGATTTAAAAG[-/T]TAACTATAAACATAA	161436
rs538889684	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88694066	GCATGAGTCACTGTG[C/T]CCAGCCAATGTTGAC	161436
rs538903732	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770977	TGTCATCAAATCCCA[A/C]AATTACATATTAAGT	161436
rs538905417	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666381	ACAGGCATGTGCCAC[C/G]AGGCCTGGCTACTTT	161436
rs538927234	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88693473	CAAGAACAGTATGGC[A/G]AACCGCCCCCATGAT	161436
rs538930155	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619938	CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC	161436
rs538931109	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88683525	CAAAGCCAGACAAAG[A/G]TATCACAAGAAAACT	161436
rs538978818	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657729	TTAAAAAATAAGTTC[A/T]ATATGACCATACTTT	161436
rs538996091	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649619	ATGTGTGGTTAGGTT[G/T]GTTTTTACGAGCCTC	161436
rs539011874	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763070	GGGAAAGATCTAAAA[C/T]CGACACCCTAACATC	161436
rs539031360	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88748106	AGACTTACTAATTTG[A/G]ACAAACAGAGCCTGG	161436
rs539050168	in-del	-/AA	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88706060	GATTAAAACGCAATC[-/AA]AATTACTTTGTATTT	161436
rs539053536	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759542	TAAAACAACTAGCCA[C/G]GTGTGATGGTACATG	161436
rs539068219	snp	A/C			upstream-variant-2KB	EML5	GRCh38.p7	14:88794648	TGATTATTTAAATTC[A/C]AGCAGTGAACTTAGA	161436
rs539071912	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88670948	GAACCTATGACTGAC[C/T]GGGGTACCTGAACAG	161436
rs539095909	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671847	AATTCAACAAGTAAA[A/G]CTAACTATCCTAAAT	161436
rs539105844	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617902	GCATTCCTTTAGATA[A/G]AGAATTAATAACAGT	161436
rs539125502	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88715526	AGAAGTTCTTTGTAA[A/C]TATGGAGTTTATGAA	161436
rs539132520	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668398	AGAAGAAACAGACAC[A/G]CACGGGTTCCAGAGA	161436
rs539150686	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765459	CTTCCAATCAGCAAC[A/G]GCACATTGAGTTCTT	161436
rs539150964	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	EML5, ZC3H14	GRCh38.p7	14:88614848	TGGAGTGGCACACAT[A/C]TAAACAAATTTTCCC	161436
rs539162443	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722973	ATTATAGAATCTGTA[C/T]GTAACACAGCAATAA	161436
rs539163379	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622853	TTTACCTCTAATATT[C/T]TTGTAAACTTTCTAT	161436
rs539182131	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643619	ACTGTATTTTTTGTG[G/T]CCAAAAGAAGAAAAT	161436
rs539192717	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88783507	AATAGAAACCAAAAA[A/T]GAGCAGGAGTAGCTA	161436
rs539218353	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640016	GAAGTAAAATGAAGA[A/G]GTGGAAAATGAGTTC	161436
rs539221426	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737700	TTGTCCATGTTGTTT[A/T]CTACATGAAATATTT	161436
rs539240380	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650240	GGTGAATCACTTGAG[G/T]TCAGGAGTTCGAGAC	161436
rs539250049	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88745640	TAAACAGACCCTAGG[C/T]TCAAACCATTCAATT	161436
rs539258944	in-del	-/AATA	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88749604	ATATGTAGAAGTATT[-/AATA]AATAAATGACGATAG	161436
rs539274405	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88754739	TTTTATAGTATTTGG[C/T]AGATGTAAAACACAT	161436
rs539281014	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646590	AGGTAATTTTTATCT[A/G]TATAATCCTATATAA	161436
rs539293125	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691010	CCAGGGTCTGCCTCC[C/T]TGGTTTGTGGCTGTA	161436
rs539298135	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700798	TCGTAAACCATTAAA[C/T]ACAACTGTGCATCCA	161436
rs539308057	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88750511	GAGTGCCTGGTATAT[A/G]ACTGATGTTACATAA	161436
rs539331200	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690546	TGGTGAGGTGAAAAA[A/T]ACTAGATTAGACTTT	161436
rs539334085	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698041	CGCACCTGGCCGAGA[C/T]TGATTTTATAAAAAG	161436
rs539337202	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758753	ATCATTCACAAATGG[C/T]CAAAAAGTAGAAACA	161436
rs539372380	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705209	GGAAATTTTTATACT[C/T]CATAAAAGAATATTG	161436
rs539450750	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758727	ACTTGTACACAAATG[C/T]TCACAGCAGCATCAT	161436
rs539490996	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696539	CAGTGCCCTCCCAGC[A/G]TGGGAGATGCAAACC	161436
rs539497051	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785801	CTCCTAAGTGGTCTC[C/T]CTGCTTCCATCCTGC	161436
rs539501583	snp	G/T	0	0	intron-variant	EML5	GRCh38.p7	14:88747388	CTGCACTCTAGCCTG[G/T]GAGACAGAGAGAGAC	161436
rs539524485	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613933	CTGATGACTACTTAG[C/T]CAATATGACCTTTAG	161436
rs539534649	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88712220	TTTCTGCAAGAACAC[A/G]AAAGTCTTCTGTGAG	161436
rs539541344	snp	A/C/T	0.000176526	0.0093935	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705486	TGGAAAATTACCTGT[A/C/T]GACGGTAGGTGAGCT	161436
rs539577741	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719871	TTTTGAAAAAATTAA[C/T]AAAATAAATAGACTG	161436
rs539581192	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88709571	TTACACCAACTGGGT[C/T]TGCAAAAGTTAGAAA	161436
rs539620094	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88679046	GTTTATAGGTACATC[-/A]CTCCAATCCTCTGCT	161436
rs539628071	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734894	AAGAGACTGAAAAGA[C/T]ATATCAGCAAACGCA	161436
rs539652564	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641132	GTAATAAAAAACCTA[C/T]CAAAAAGCCCTGGAC	161436
rs539664229	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742071	TTAGCTTCACATTAG[A/G]ATCACCTGGGAAATC	161436
rs539666022	in-del	-/A	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774838	AATCTATACCAGCTC[-/A]GATTGCTTCCCTGAA	161436
rs539684395	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779073	CAATGTTCAAGGTAA[C/T]CACTGCTCCATTAGT	161436
rs539685603	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88772309	TACCATTATTCCTCT[A/G]TTGCTTCCCTTTAGA	161436
rs539710188	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88744184	CCCAAACTCCTAATC[A/G]TAAAATAATATTCCT	161436
rs539728426	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88629413	AAAACGTATAGGTAC[G/T]TAAGGTAATGGAATT	161436
rs539748817	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88786922	AAATCATGATGAAAA[A/G]TCAAATAAGATGAGA	161436
rs539755459	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646027	CAAATACTGAATAAC[C/T]GGAACATTGAATTTA	161436
rs539789179	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638140	TTTACAAACGTATTG[A/T]AGTTTATGAAACTTC	161436
rs539807953	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88684374	ACGGGGTTTCACCGT[A/T]TTAGCCGGGATGGTC	161436
rs539866440	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632390	TCAAAGTATAAATTC[A/G]GTCATATCACTCCCT	161436
rs539866502	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623773	TCAGGTGTTAAAATA[C/T]CTCACTGGAACAGTT	161436
rs539867606	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729459	AATGGTTGAAAAAAA[A/T]GTTTTAATAAAATTT	161436
rs539898386	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88623444	TTATTTTTTTGAGAC[A/C]GAGTGTCGCTCTGTC	161436
rs539951603	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647528	ACTGTGAGACCCCAT[C/T]TCTATAAAAAACACA	161436
rs539965172	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631588	AGCCTAGCCAACATG[C/G]TGAAACCCCATCTCT	161436
rs539982216	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735689	TCAGAGATATTCATA[C/T]ATGTACAAAATGACA	161436
rs540015020	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656344	AAGCTGGAAACCATC[A/C]TTCTCAGCAAACTAA	161436
rs540033552	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88627431	ATTTATAATGCTAAT[A/G]ATGGTTTCATTAATT	161436
rs540035814	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88726790	CTAGATATCTTAACT[A/G]TCTGTTGTGTGGCAA	161436
rs540068700	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761906	TCGTATGAGATGATA[C/T]CATACTGTGGTTTTG	161436
rs540070119	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88675352	CCAAACCTCAATTCT[C/T]GACTTCTGTGCACCT	161436
rs540074751	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655590	TCATGACTAAAACAC[C/T]GACAGCAATTGCAAC	161436
rs540096090	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682985	ATCCAGAAATCCAGA[C/T]AGCTCCTAATCTCTT	161436
rs540111073	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663214	TATGGGAAAAAATCA[G/T]CTTAAATATAAAAAC	161436
rs540144103	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689721	CCTGCGTGACAGAGC[A/G]AAACCCTGTCTCCAA	161436
rs540154728	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88682231	TTAGCTCCACAATTA[C/T]CATATAATCAAGCTA	161436
rs540174874	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732918	CAGGTTCTAGCGATA[C/T]TATTAAACACTGAAT	161436
rs540175367	snp	C/T	0	0	intron-variant	EML5	GRCh38.p7	14:88670237	GAGGCAGAGAATTGC[C/T]TGAACCCAGGAAGTG	161436
rs540263165	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760294	TCTTACATTTAAAGC[G/T]ACAATCTATTTTGAG	161436
rs540322271	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88686280	AGAGTGTGGTGCTAT[C/G]CCTTAAAGGAAGAAA	161436
rs540328516	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88723150	GGGCACAGGGGCTCA[C/T]GCCTGTAATCCCAGC	161436
rs540333744	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684560	TTAGAAACTTAAGAA[A/T]GGCCTAATGAAGAGT	161436
rs540344800	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691855	GCCTTAACATTCATC[C/G/T]TTTTATGCTTCACTT	161436
rs540348887	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640595	AGTGCTAAATGCCTA[C/T]CTCAAAATGTTAGAA	161436
rs540349351	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789417	TATACACAAGTAGAT[A/G]GCAAAAAGAAGATGG	161436
rs540391121	in-del	-/GA			intron-variant	EML5	GRCh38.p7	14:88689859	CTAGAGCTTCATGGT[-/GA]GAGAGACAGTCAATA	161436
rs540401679	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707205	ACCCAATTTCTCCAA[C/T]AATAAAGGAATCATT	161436
rs540403204	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88789126	AAAGTTTCAAAATAT[A/G]GACCAAGGTATAGAT	161436
rs540408872	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743293	CTAAAACAAAGAAAT[A/G]GCAAATGTTTGGGAT	161436
rs540431193	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691450	CTTTGGTTCAGAGCA[C/T]TGACAGCTGGGTTTT	161436
rs540436500	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88619587	TTTTCTTCCATCTGG[-/A]AAAAACGTTGTCTTA	161436
rs540438625	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706204	AAATTGTTATTTGGG[G/T]GTTACTGAAGAATTA	161436
rs540459459	snp	C/G	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88640152	ATAGTGTTAGATCAT[C/G]AAGGTAGAAAACTAA	161436
rs540472029	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646905	TGGAAGATGACAAAA[A/G]TACAAAGTTAGGCTT	161436
rs540509157	in-del	-/TG	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88771348	ATTCACTAATCTAAC[-/TG]TACTGGCAGACTCTG	161436
rs540527035	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751019	ATTGGCCAAAAACTT[A/T]AAAATTCCATGTATC	161436
rs540532637	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88774515	TACACAGTCTTTTGG[A/G]GAGTCTTATGATTAC	161436
rs540556696	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88623075	GGCTTGAGTGCAGTG[G/T]CATGATCTAGGCTTA	161436
rs540568096	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698337	ATGGCATGATGTTGG[C/T]TCACTGCGACCTCCG	161436
rs540608883	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653768	TTTTCTTTTTTTGTT[A/G]TGTCTCTGCCAGGTT	161436
rs540615671	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750135	CTATTTCACTTACTA[C/T]AGACAGCTTATCAAA	161436
rs540654241	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88759117	TAAAAATCACTGAAT[C/T]GTGCACTTAAAGTGT	161436
rs540714592	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88721596	TGGACCCCTTCCTTA[C/T]ACCTTATACAAAAAT	161436
rs540714718	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88759516	CAGCAAGACCCCACC[A/T]CTACAAAAAATAAAA	161436
rs540715267	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709083	AAATATTTTCAATAT[A/C]TGGTATCAATATGAC	161436
rs540739287	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88668289	TGAAAAGAAAAGTCC[A/G]GGGAGAAGCGCTGGA	161436
rs540759448	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614633	TTTTTAAATAGCAGT[C/G]TACATAATTTTCAAT	161436
rs540769180	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623060	TCGCTCTGTCTCCCA[A/G]GCTTGAGTGCAGTGG	161436
rs540782622	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665260	ATAACATAACAGTTA[A/G]TAAAAATTATACATT	161436
rs540787491	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788566	GTACTCTAAATTCTA[C/T]ACCTACTTAATACAT	161436
rs540807532	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88731759	TTTTAATGATCACCA[C/T]TCTAACTGGTGTGAG	161436
rs540886454	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88646285	AATGGGATGTTGATA[C/T]GCAATATGAGGCAGC	161436
rs540985685	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791917	CTTTATTAGGTAAAG[C/G]GTTTCCCCCCACCCC	161436
rs540991364	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686151	CCTAGAAAAAATCAG[C/G]TTTGATATTTGAAAA	161436
rs540999578	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88641662	CAAACTAGGAATTGA[A/T]GGAACACACCTCAAA	161436
rs541008201	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650804	GTACTACCATTCTTG[G/T]CTAATTTTTCTATTT	161436
rs541068891	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642105	CGACAAGAGGTGGTG[A/G]ATTATAATTCACATC	161436
rs541071575	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88658042	TGTTCTTGAGTCACA[A/G]AATGGATTTTGATGT	161436
rs541076635	snp	A/G			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615617	ATGGCATTATCTGGC[A/G]GTGTATGGATTACGG	161436
rs541089686	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649083	TGCCCAAGCTGGAGT[A/G]TAGTGATGCCATCAC	161436
rs541112667	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88737529	AGGGGCATTGCGCCC[A/G]CCATGGAGGTCTCCA	161436
rs541114550	in-del	-/CTTC			intron-variant	EML5	GRCh38.p7	14:88770914	TTTTTTAAAGTTCTT[-/CTTC]CTATTAATATTGCTG	161436
rs541124163	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88744817	TCAACCTACCTCTAA[A/T]AGGTTTACATTTTTG	161436
rs541133499	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88769960	TAGATTACAGCATTA[C/T]GTGCAGTTTTTTTTT	161436
rs541133798	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672696	CACAATAAAAAATGA[C/T]AAAGGGGACATCACC	161436
rs541145826	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704010	ACTAGCATTGCCTTA[C/T]TCACTCCTCATCAGA	161436
rs541164974	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693022	TATTTAGAAAACAGA[A/C]ATTTTTTATTTTATA	161436
rs541168672	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88745217	AGGCCTCTCTGTGCA[C/T]CTACTAAAAACCAAA	161436
rs541175996	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619304	CAGGAGGCACAGGTT[A/G]TGGTGAGCTGAGATT	161436
rs541186121	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88785211	TGGAGGACTCAGGGG[G/T]AAGTGGGGATGGTTA	161436
rs541222476	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644698	AGAAAGAAAATATTA[C/T]AACTTTTATTCATTT	161436
rs541232467	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715918	TTTCAATGATGACTT[C/T]TTATTGAGTATCCAA	161436
rs541237008	snp	A/C/T	0.000239747	0.0109465	intron-variant	EML5	GRCh38.p7	14:88738864	CTAGTAATAAGACAT[A/C/T]TGTTTTGTTATTACC	161436
rs541248272	snp	A/G	0.0158469	0.0875917	intron-variant	EML5	GRCh38.p7	14:88660187	ACTCAAGAGGCTGAG[A/G]TGGGAGGATAACTTG	161436
rs541255279	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88680845	AAAGTCCAATCAAAC[A/G]TGAACTTACAATACA	161436
rs541290552	in-del	-/CA	0.0279526	0.114869	intron-variant	EML5	GRCh38.p7	14:88714553	CTTAAATGTTCTCAC[-/CA]CACACACACACAAAA	161436
rs541310840	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750128	ATATTTACTATTTCA[C/T]TTACTATAGACAGCT	161436
rs541351615	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679623	CTTGAACCTGGGAGG[C/T]GGAGGATGCACTGAG	161436
rs541379819	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787711	AAATCTTACCAAATA[C/T]AATTGTTACATGGTC	161436
rs541380807	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783145	GTCCAGGTAGAGGTA[C/T]GTTGCAGGGGCGGAG	161436
rs541403109	snp	C/T	1.67041e-05	0.00288994	intron-variant	EML5	GRCh38.p7	14:88643029	CACAAGGTCCTATAA[C/T]GATAATAATAAAACC	161436
rs541418050	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88737208	AACAGGAGAGGGAGC[C/T]GCTGGGCACCACATG	161436
rs541435688	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88745282	TCTACCCAACTTTTA[A/G]AATGATAAATTCCCA	161436
rs541445954	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88784018	AGAGGAATACAAATA[C/T]GTGGAAATTAAACAA	161436
rs541452580	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639320	GGCAGGAAAGTGTTG[C/T]GTATCCATATAACAG	161436
rs541480862	in-del	-/TGTCT	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88693149	TTAGACTATAGAACA[-/TGTCT]TTAACAGAAGAAAAA	161436
rs541492540	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645593	AATCACATCCGAGTT[C/G]AAATTTGTATTTATC	161436
rs541580779	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88724269	ACAGAGCAAGACTCC[A/G]TATCAAAAAAAAAAA	161436
rs541600190	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618705	ACAAAGCTTGGAATG[C/T]CTTTGCAGTAGCTGA	161436
rs541600198	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626611	GACAGAGTGAGATAC[C/T]GTGTCAAAAAAAAAA	161436
rs541650369	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777354	AAATTATCCCTCAAC[A/G]TGAAGGAGAAACAAA	161436
rs541652348	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88690036	GACTTGAAGGAGGTA[C/G]CAAGAGCAAGCCATG	161436
rs541669973	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625912	AAGGATTTATACAGC[C/T]TAGCCAATGCAGGAT	161436
rs541671482	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761240	AAGTTCTGAGATACA[C/T]GTGCAGAACGTGCAG	161436
rs541683330	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676597	ATTCCCAATAAACTA[C/T]CATTGACATTCTTCA	161436
rs541704155	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780511	AATTGGCTCACATGA[C/T]TGTGAGGATCGACAG	161436
rs541705520	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773415	GGCCTTAGGCAAGAA[A/G]CCCAAAGTATTTAAG	161436
rs541735319	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88634899	TTCTTTCTTTCAACT[A/G]AAGATTTTCCGTATG	161436
rs541736858	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779674	GCTCTCTGATGTCAA[G/T]ATATTCTAGGCGCAA	161436
rs541773230	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88732568	TTTTTTGATTCCATA[C/T]GAACTTTAGTTTTTT	161436
rs541781758	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88621745	ATAAGTACAAACACG[C/T]TCAAAAATTTTCATA	161436
rs541787219	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630760	CTGAAAAGGATTTTT[C/T]TGCTTCTTTCCCACT	161436
rs541788949	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730681	ATGCAAAGTGTGAAG[A/T]GACAAGAATTTGCTT	161436
rs541812738	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638631	TCAGATAACCAGAGT[A/G]AGTGAGAGAAAGGTA	161436
rs541828382	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726228	GATCATTACTGAAAA[C/T]CTATACTAACAGGAA	161436
rs541844851	snp	G/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88620571	GTTGGTGCCCAGTGG[G/T]TTTATAATTTAGCAA	161436
rs541845491	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683509	ATTATTACCCTGATA[C/T]CAAAGCCAGACAAAG	161436
rs541873054	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628804	TGATAAATTAAATCT[A/G]GCAGTTCTTCAAAGC	161436
rs541884445	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690199	GGGGTTGGAGAGGTC[A/T]AAGGCAGTACTGCAG	161436
rs541923450	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697761	TTTTTTTGAGATGGA[A/G]TTTCACTCTTGTTGC	161436
rs541948467	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698352	CTCACTGCGACCTCC[A/G]CCTCCCAGGCTCAAG	161436
rs541955160	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88627576	ACTTTAAGACAAATA[C/T]TAAATACAGAATTCC	161436
rs541976436	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88712598	TCTTCCCACCCCACT[C/T]AGAGGAAAATACATA	161436
rs541982820	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638134	ATAAATTTTACAAAC[A/G]TATTGAAGTTTATGA	161436
rs541983181	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689412	CACACTAGGGAATAC[A/G]AAATACCAACTGAAT	161436
rs541985677	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637670	TTGAGTAAGTGAATT[C/T]ACTCAATAAAAATTA	161436
rs541985682	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88668486	GCTGTGAGGTGAATA[A/C]ACTGAGAACCAGGAA	161436
rs541999942	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725728	GGGAAACCAAACAGG[A/C]GGTAAGAAGATCAGC	161436
rs542008854	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720292	CTCATTTTATGAGGC[C/T]AGCAACATCTTGATA	161436
rs542023258	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631320	CTGGGCTCAATTAAT[A/C]TACCTACCTCAACCT	161436
rs542092227	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756980	ACTGACAAGCTGATT[A/C]TAAAATCCAGAAAGA	161436
rs542092297	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765493	AAGCTTTGAATCTTT[A/C]TGACTTCTGCTGCAT	161436
rs542097666	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660275	GTCACAGAGAGAGAC[A/G]CTGTCTTAAAAAAAA	161436
rs542108243	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668115	TAGTACTAGGGTTGC[G/T]GCTTTCTATGGTGGC	161436
rs542126974	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764988	CCATGACTAGCTCAT[A/G]CTGTTTTCTATGCCA	161436
rs542169994	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772384	TGATCTCATCATTTA[C/T]CTCGGTAAAAACCCA	161436
rs542173965	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88684359	GTATTCTTAGTAGAG[A/G]CGGGGTTTCACCGTT	161436
rs542183231	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88727663	TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG	161436
rs542226983	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714871	AATGTAACTTACACT[C/G]TGCTTCCAGTAAAAC	161436
rs542234417	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617138	TTATGAAAACTGATA[A/G]AACTATTTTTTCTTT	161436
rs542243686	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664198	GGGAGGATGACTTAA[A/G]CCCAGGAGGTTAAGG	161436
rs542257138	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771754	CCATTTTTCAGTAGT[A/G]TTTGACATAACTGAC	161436
rs542278394	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88788900	CCCCATCTTTACCGA[-/A]AAAAAAAAAAAAATA	161436
rs542279138	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666852	TTATAGCATAAGTTG[A/G]GAACAAGTAGTCATT	161436
rs542292078	in-del	-/T	0.37955	0.213815	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768417	CGTAATGTGATTGTC[-/T]TTTTTTTTTTTGAGA	161436
rs542331986	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682567	CTTCCTCCCTCCTCA[C/T]CTGGTTGGAAACTCC	161436
rs542344021	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88681810	CCTTTTTAAAATGTG[C/T]CTAGTTTTGCTTTCT	161436
rs542352621	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729841	ACTGGGATTACAGGC[A/G]TAAGCCACCACACTC	161436
rs542353027	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721941	AAACAACCCCATTAA[A/G]AAGTGGGCAAAGGAC	161436
rs542364603	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88785872	GTGACTTTGTTAAAC[C/T]GTAAGTCAAATTATG	161436
rs542390662	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624230	TACAGGCATGTGCCA[C/T]CACACCCGGCTAATT	161436
rs542422424	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649103	GATGCCATCACAGCT[C/T]ACTGCAGCCTCAAAC	161436
rs542438938	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88754110	CAGCCTGGGCAGCAG[A/G]GCGTGACCCTGTCTC	161436
rs542445799	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745385	TTAGACACTTTTAGG[A/C]GTTTACAACTTTTTT	161436
rs542461863	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88657869	AATACATTTTCTATA[A/G]CGAGCTGATATTACT	161436
rs542462445	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613173	CTTTGCTGTGCTGAT[C/T]CCACAGGAAAGGCTT	161436
rs542467768	in-del	-/CTT			intron-variant	EML5	GRCh38.p7	14:88687856	GAGGTGGGAGAATAG[-/CTT]CTTAAGCCCAGGAGT	161436
rs542516260	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88762140	GTAGGTTGCCTGTTC[A/G]CTCTGATGATAGTTT	161436
rs542525151	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667584	TAATTTATTGCCTCT[A/C]AGTTCCAAATCTGCC	161436
rs542527878	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656563	ATGGCACATGTATAC[C/G]TATGTAACAAACCTG	161436
rs542543791	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677261	CCACATGCAGAAAAT[C/T]GAAGCTGGACCCCTT	161436
rs542557663	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613557	ACACATATTTAAGAG[C/T]TTAATCTTTCAGTTG	161436
rs542559124	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618398	ATCCACAGGGGGTTT[A/C]CAGAATACTAGCATA	161436
rs542562090	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750007	AGTTTTACTGGAATA[C/T]AGCCACACTCATTCC	161436
rs542632115	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756489	TTAACTTATTAGATA[C/T]TCTAGCCAAGAAAAA	161436
rs542655090	in-del	-/AT	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88629187	CTCTAGGCAATTCAC[-/AT]GTTATATTTGCCAAA	161436
rs542697621	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88654823	AGCTGAGTTCAACTC[C/T]TGATTATCCTTGTTA	161436
rs542705923	snp	C/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88753927	GAGGATAGCTTAAGG[C/T]CAGAAGTTTGAGACC	161436
rs542706645	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670347	AAAAAGGAGAAAAAA[G/T]AAAAACAAACACCAA	161436
rs542707948	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662250	CACTTTCATGTTAAA[C/T]TTGTTAAGCCTCTCT	161436
rs542727334	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88669417	TGGTGCCTGGGAAAA[C/T]AGACAGTTTAGACCC	161436
rs542733108	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88680618	TACTCATTATAGTAC[C/T]AGCTTTCAAATTTTT	161436
rs542736186	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633530	GATGGAGATTTACTG[A/G]TTAAAAAACAAAATA	161436
rs542759771	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782292	AGATGATTTAGGGTA[G/T]CTGGTGGAAGAAATT	161436
rs542767555	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678495	CCTAACGGCATAGCA[C/G]ACTAGTCTTGCACCT	161436
rs542774036	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88643406	AAAATAACATTTAAA[-/AC]ACAATATTGTATAAC	161436
rs542779615	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713507	GTTAGAGCCACGATC[C/T]TGCTCTTTCACCCAG	161436
rs542791602	in-del	-/ACATT	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88685238	TTGACAGTGAAAATC[-/ACATT]ACAAGGTTTTCTCCT	161436
rs542845219	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88632578	CCTCAGGGTTTATGC[A/G]GGAAAGATTTAATAT	161436
rs542865406	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735800	GATTAGTTGAATAAA[C/T]TACAGTATATCCATG	161436
rs542872825	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762438	TCACTTGAACCCGGG[A/G]GGCAGAGGTTGCAGT	161436
rs542887929	snp	C/T	8.61111e-05	0.00656111	intron-variant	EML5	GRCh38.p7	14:88685190	ATACAGTTACTATAA[C/T]ACAACAGTGTATATA	161436
rs542899770	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708222	ATTTTTAATAACTTG[C/T]TCTGATAAATGGGTA	161436
rs542929570	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698878	TTCTAAGCACCTTAC[A/G]AACATTGACTCATGT	161436
rs542934219	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88715822	TGCACACCACCATAC[C/T]CGGCTAATCTTTTTG	161436
rs542935204	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88699835	CTAAGAAGGAAACAC[A/G]AAACGATGAACAGGT	161436
rs542940177	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88657921	AATTATTTTAAAATA[G/T]GAGGTTTAATAATAT	161436
rs542943546	in-del	-/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778370	ACAAGAGTTAAAAAC[-/T]TCAATTTTGAGTGTA	161436
rs542968876	snp	C/T	1.89888e-05	0.00308124	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88695375	CCTTGCTATTGAAAG[C/T]TTCTCTCCTTTCTTC	161436
rs542995785	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88742623	CATAATTAATTTGCC[A/G]ATCACTTATTAAGCA	161436
rs543006657	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703181	TGTATAGTATACTAC[C/G]ATTTACATAAGTATA	161436
rs543046860	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88725441	TGGGGAGATGTTAGT[G/T]AAAGAGTACGAAGTT	161436
rs543061497	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659717	AATATTTTAGTGGAA[C/G]ACATTGTTAACAACT	161436
rs543080705	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760885	GCATAGATTTTGTAA[A/T]ATTTATATAGATATT	161436
rs543117478	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760468	AAAAATCAATTGACC[A/C]TATCTATATTACTTT	161436
rs543130975	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88783911	AGACTGTGTGTTGGG[A/T]CATAAGACAAGTCTT	161436
rs543162812	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790786	TAGGGAAAAAGACAA[C/G]ACACTGGGGTAAACT	161436
rs543164441	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700034	ATACTACATTGTGAG[C/T]TCCCGATAGTGGCAG	161436
rs543184576	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736226	GGATGGTCTCAATCC[C/T]TTGACCTTGTGATCT	161436
rs543197660	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726401	TAACATCTGAAATAT[A/C]TTAATAAGAAGGGGA	161436
rs543206771	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88736857	GTGCCCATCTTTGAG[A/G]GGTGCTTTTTTTAAG	161436
rs543295754	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88689344	CAATGTACACTCCTA[A/C/T]GAACAGTGAAAAGAA	161436
rs543308622	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647955	TTCAAAGGAAATTGT[C/T]TAAAGAGCCTAAGTT	161436
rs543310568	snp	G/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88640159	TAGATCATCAAGGTA[G/T]AAAACTAACAAAGAA	161436
rs543322045	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691552	TCAAAAACTTTCAGA[A/G]GCTCCCCATCCCTCT	161436
rs543328012	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696103	TCCAGTGGTATTTTT[C/T]GTGGTGACTCACTTA	161436
rs543334925	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789641	AAGAACCAGTAAGCA[A/C]ATGATAGACTAGTCA	161436
rs543343897	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703154	GTGAAAAAAACAAGG[C/T]AGAAAATAGTATGTA	161436
rs543379145	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88676394	AAGGAGGTGAAATGC[C/G]AGACACATGAAACCA	161436
rs543430574	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747659	AAGAATACGAGACTA[C/T]AAAAAGTATCCAAGG	161436
rs543469350	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88747130	CAAACAAAAAAAAAA[C/G]GGTCAGGTGCGGTGG	161436
rs543472313	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635011	GTATAACTCAAGAAA[C/G]GAAAAAAGTTCTTTC	161436
rs543479426	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88658946	AAAAGTAACTATCGA[C/T]TGATTGCTTTGGTAC	161436
rs543483281	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695029	TCTTTTTTCACTTTA[A/G]TATATAATATAAGCA	161436
rs543488640	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648424	AGTGGTGTGATCATG[A/G]CTTACTTGAGCTTTG	161436
rs543499544	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783357	AAAGAAATAGAGTAG[A/G]TGAATGGATGAACAG	161436
rs543500457	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88774865	TGAATTATAGACATG[A/T]ATGTTCAACAGCCTA	161436
rs543504210	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763973	AAATTCTGTCAAATG[C/T]TTTTCCTGTAACTAC	161436
rs543514645	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88737339	CACATTCCCTTCAAC[C/T]AGACGCCAACGCCCA	161436
rs543521795	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766465	GATGAAATAAGCCCC[A/G]GTCTCCCATAGCGCT	161436
rs543532957	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709946	ATGAATTTCCTGGAA[C/T]CTAAATGATATTTTC	161436
rs543549479	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687080	TGGTATCCAGTTAAG[C/T]GATTTCTTCCACTTA	161436
rs543558303	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767973	ACTGTTATTCCTCCT[C/T]AGCAACTTCCAGTCT	161436
rs543565740	in-del	-/A	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88783502	ATGCCAATAGAAACC[-/A]AAAAAGAGCAGGAGT	161436
rs543578500	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792033	TCGTAATTGTGATGG[A/G]GTGGGAAAGGGGACA	161436
rs543589038	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612135	GATGCAGTGAGGCAG[C/T]TGTCATTATTCTAAA	161436
rs543593279	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777989	CAAAAAATACAGCAA[A/T]TTTTTAAAAATGAGG	161436
rs543597475	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722944	TCATAAGAGCTAAGA[A/T]AACATGGTGAGAGAT	161436
rs543599453	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88638424	CACGGAAGCAGGGTT[C/T]TACCCCGCCCAGTCT	161436
rs543656370	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88673338	ATAAAATTCAACATC[C/G]CATCACGTTAAAAAT	161436
rs543657417	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716869	CTCTCACATGAAGAG[C/T]TTCTCTGACAAATTT	161436
rs543658513	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666058	ACTTCTGAATACAAC[A/C]AAAGCAAGTATGGAT	161436
rs543660258	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637783	TTGTTCCTTGTGCAC[A/G]GTGAAAATAAGACTT	161436
rs543663058	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740047	ATTTAATTGCCTCTG[A/G]TAAATTAGCCTCAAG	161436
rs543685109	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88774253	TTTAGTAACTTTCCA[C/G]GTGATGCCGTTGCTA	161436
rs543689059	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776886	ACCCCGTCTCAAAAA[C/T]GAAAAAACAGAAACA	161436
rs543689761	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785975	ATAAAATCTGCCCCC[A/G]CCACCATAGCTCATC	161436
rs543694114	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763619	CAGAACACTTCCAAA[C/T]AATAGAAAAAGAGGG	161436
rs543719046	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681601	AAATTATGTATAATC[C/T]ATAGTCACAAAGGAG	161436
rs543724829	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776030	TCAAGGTGGCACCTC[C/T]ATGAGTCTGCAACAA	161436
rs543763277	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631408	TTTGTAGAGATGGGG[C/T]TTGCCATGTTGCCCA	161436
rs543763381	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88689198	ACATTCTTGTAAAGG[A/C]CTCTTCTATACAAGT	161436
rs543773146	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645095	GCCGTGGCACATTCT[C/T]GCCTCACTGCAACTC	161436
rs543774205	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88745722	CTTCACACCTTAAAT[A/T]TGTGCATCCCTATGT	161436
rs543812762	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737878	ATTACCTTTATAGAA[C/T]TGTATTCTTTTCCTT	161436
rs543826096	snp	G/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88640146	CCACTGATAGTGTTA[G/T]ATCATCAAGGTAGAA	161436
rs543826157	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630851	ATGCAACCAGCCTTA[C/T]CGGTGAAGCCAACAC	161436
rs543868251	snp	A/C			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616876	AACCTCATCTCCTAG[A/C]ATACTAGAGGGAAGG	161436
rs543891382	snp	C/G	0.00398564	0.0444627	upstream-variant-2KB	EML5	GRCh38.p7	14:88792887	CCTGCGGCGCTCGCG[C/G]CCCGCCGCGGCTTTG	161436
rs543950576	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693633	TATTTGTTTAAAATG[C/T]ATCAATACAACAGTA	161436
rs543962209	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88788363	ACGATTTACCACAAA[A/T]AAAGAAAATAGCTTC	161436
rs543985242	snp	A/G	8.7831e-05	0.0066263	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88663097	TTGTTCCTTAGCACC[A/G]GTGTTGACCTGTAAA	161436
rs543989735	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88620345	AATAGGTATTGATTA[A/T]ATTAATGAACTACAT	161436
rs543999287	in-del	-/A	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88631102	ATTGCCTTAAGGATC[-/A]AAAATATCAAATTCT	161436
rs544022200	in-del	-/TCAA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88685295	TGTACTATATTAACC[-/TCAA]TCATTCAATTTAGTA	161436
rs544033376	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770660	TTAATGAGAATGAAA[A/G]CATGAGTGTTGTTCA	161436
rs544033895	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725542	ATAGATGAAAGAAAC[C/T]GGGGTACTGAGAAAT	161436
rs544049153	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88784576	TATACAACCTACCAA[C/G]ATTGAACCAGGAAGA	161436
rs544050350	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88619376	AACTCAAAACAAAAC[A/G]AAACAAAATTTAATT	161436
rs544061413	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669503	CCTCTTTAGGTCGGA[A/C]CCTGACCATAACCCC	161436
rs544084380	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88787747	ATAAATGTTAAGTCC[A/T]TCTAATTCTAGTTAC	161436
rs544095634	in-del	-/T	0.0142736	0.0832652	intron-variant	EML5	GRCh38.p7	14:88660569	AACATGGTAAAACCC[-/T]ATCTCTACTAAAAAT	161436
rs544113379	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781389	ATGTAATAGATTTAT[A/G]AATCAGAATGTCCCC	161436
rs544118181	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680939	AAACAAAAAAACAAG[A/G]AAACATCCAAAAGAA	161436
rs544126695	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626717	AAATATATGCTTGAC[C/T]AGGGCATGTAATGAT	161436
rs544166167	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720153	AGTAATAAATAGCCT[A/G]CCAACCAAAAAAGGC	161436
rs544168340	snp	G/T	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614499	ATCTTCATATATCCT[G/T]TCAGACCAAATGGGA	161436
rs544204545	in-del	-/CTC	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88671331	TGAAGGAGAAATAAA[-/CTC]CTTTTTAGACAAGCA	161436
rs544221657	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88623664	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGTT	161436
rs544289927	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684101	GAACTAATAAATGAG[C/G]ACGGCAAGTTTACAG	161436
rs544304915	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691256	CCAACCAAAACCTGC[C/T]AGACCCATTCCCTGG	161436
rs544322119	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787834	TCTACATATTGCACA[C/G]TGCTTAAGAAAACTC	161436
rs544343484	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690692	GTTTTGTGTCACTTA[C/T]TTAAGATGGCGAAAT	161436
rs544346637	in-del	-/GACT			intron-variant	EML5	GRCh38.p7	14:88656751	TTTGAAATGAGGACT[-/GACT]ATGCTTAAAGAAAGG	161436
rs544348123	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726929	GTTGGAGTGCAGTGG[C/T]GTGATCATAGCTTAC	161436
rs544354580	in-del	-/AA	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88725967	ACTGAGGTAGAGAAG[-/AA]AGACTTCGTAAGTAC	161436
rs544363970	snp	C/T	4.97236e-05	0.00498591	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616841	TCAGCTTTCTCAGCA[C/T]GTCTGGACCAGATTC	161436
rs544390760	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750949	GCACTGCTGTTCTTT[C/T]TACTAATGTCTCCTC	161436
rs544400108	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88683176	ATAAAAAGTAATTGG[A/G]AGGAGACTGGTAGGC	161436
rs544426216	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713609	AGGTGCATGCCACCA[A/C]AACCTGCTCATTTTT	161436
rs544429962	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769040	TAGTTCTTAAATGCA[C/T]AGAGGTCTGATTGCA	161436
rs544430780	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749956	AAGTACAACTCTCAA[A/G]CCAAATCCTGTCTGT	161436
rs544474065	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646237	CATCAATAAAAGTAA[A/T]TGTGCTATATCTTAA	161436
rs544474467	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766920	GGGGCTGGTTTCCCC[C/T]GATAGCACACAGTTA	161436
rs544491467	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88785517	AACAGAGCTGTTGAT[C/T]TTTCCTTCTGTCCAA	161436
rs544542072	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729374	CAGCAAACCATGTCC[C/T]GTGGGCCAAACCAGG	161436
rs544548349	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88725903	GCAAAAGAGAGAACT[C/G]TGTTAATAGTTTCTG	161436
rs544549287	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615043	ACCCTTACATTGTAC[A/C]CCATTGGGAATGATT	161436
rs544566412	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88711748	GAGGACTTTAAGACA[C/G]AGCCTGGCCAACATG	161436
rs544566939	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88721172	GAAGAATGAGTATCA[C/T]GAAAATTGCCATCCT	161436
rs544577938	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716538	ATTTGGCAGCTTTTA[A/C]TTTTTATGCCTCCTT	161436
rs544599597	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88660341	ATATATAAATTTTAT[A/T]TCCGTGTTAAGGAAA	161436
rs544603951	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668506	AGAACCAGGAAGTGA[C/T]CAACAGATTGGCAGC	161436
rs544647732	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708329	AATTCTCTGTGATTA[A/C]CCCTTGTGATTATAT	161436
rs544654955	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772731	GCACTCCAGCCTGGG[C/T]GACAGGGCAAGACTC	161436
rs544662851	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668248	CTGGACAGTGACCGA[C/T]TGAATCTAAAGTGTG	161436
rs544712074	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692775	TTTTTACTTTGTAAA[C/T]GCATATGCTGTTATC	161436
rs544723351	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88741826	TGTAATAAGTAATTA[A/T]CATTTAAAATAATTT	161436
rs544730777	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778735	AGTGAGCCAAGAATG[C/T]GCCACTGCACTCCAG	161436
rs544734179	snp	A/G	0.00179243	0.0298832	intron-variant	EML5	GRCh38.p7	14:88621834	GGCATAGGGTAATAC[A/G]CATAACCATCACCTC	161436
rs544746788	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88696367	AACAAACAGAAAAGC[A/G]CTAATATGATCTGAA	161436
rs544747050	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88661517	GCTATAGATATGAAA[C/T]ATAATTCTGAACCTT	161436
rs544772353	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697835	CCACCTCCTGGGTTC[A/G]GGTGATTCTCTTACC	161436
rs544784529	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88665707	GGGCAAAGGAGAAGG[C/G]GCGAGGGGGAAGAGA	161436
rs544796222	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747052	AAATGAAGTACCGCA[A/T]CTTTGATCTATCCCT	161436
rs544797330	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671581	GTAAATTGGCTAAAT[G/T]CCCCAAATTAAAAGA	161436
rs544798738	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88713137	TGGCTCACACCTGTA[A/C]TCCCAGCACTTTGGG	161436
rs544864446	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653126	TAGAGGAATGCTTGT[A/G]ATTTTTGCACATTTA	161436
rs544922317	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88704253	AGAAACCCCCTTCCC[C/T]TTCGATCCCTTTTTC	161436
rs544934817	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708930	AAACTATAATGATCA[C/T]AGAAGCTTCCTAATT	161436
rs544945504	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88770136	TTTTTACTTACAGTC[A/C]TTTTGCAGTTTTGGT	161436
rs544946392	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649853	ACCTTAAAATACCAT[A/G]AAGAATAAAATAAAG	161436
rs544957691	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88692227	CTAAAAAATACAAAA[A/T]TCAGCTGGGTGTGGT	161436
rs544972814	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88642454	CTTAGCCTTTCTTCC[A/T]TGGCTTTCCAAGGCC	161436
rs544980997	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88754241	TGGAAAAGAGTTACA[C/T]AGAAAAATCTGTATA	161436
rs544990359	in-del	-/C	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88617388	CCGACCTCAGGTGAT[-/C]ACCCCCGCTCGGCCT	161436
rs545004808	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88665755	CAGGTAAGTAAGTAA[A/G]TAAATAGACAGGCAT	161436
rs545046421	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672145	AAATCGATCACATAA[C/T]TGAAAGTAAAACACT	161436
rs545070462	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745250	TATTCTCCAAAATGC[A/G]AATATACACAAAATT	161436
rs545108145	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88707781	TCACTAATTTAACTT[C/T]GCATAGTTCAGCCCA	161436
rs545109027	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679775	ATGTCCTTGAAGCCA[A/T]CAAACAAGAGATAGT	161436
rs545129783	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625768	ACTGAAATTTGACAT[A/G]GCACAAACATTTCAA	161436
rs545145542	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655489	ACTCAAGGTGAATTA[A/G]AGACTTAAACATAAG	161436
rs545146838	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678063	CCATCGATATTAGAC[C/T]GGATAAAGAAAATGT	161436
rs545155454	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88777629	AAATAATAACTACAA[A/C]AACTTTTTAAGACAT	161436
rs545176026	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88760983	AATATAACTAATTTA[C/T]GTATGTTGACCTGGT	161436
rs545181839	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680243	TTATTTAATTACATG[C/T]AATTTTTTTGGCAAA	161436
rs545183567	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694421	CTCTGAAATAAACAT[C/T]GAAATGTTTTAGCTC	161436
rs545185992	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	EML5	GRCh38.p7	14:88793041	CCCGGAGCCGAGAAG[A/G]GGCTGGAGTTCGCGG	161436
rs545188589	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88751229	CTAGCTTTTTATCAT[G/T]TTTTACTTTATCATT	161436
rs545198986	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650707	GCAAGGGTGCGATCA[C/T]AGCTCACTGCAGCCT	161436
rs545206596	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706179	TGAGGCCAGATTATA[A/C]TTTAATATAAAATTG	161436
rs545277903	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88618186	GATTTTCTAACTGGC[C/T]TTCAAAGTCAGTTCT	161436
rs545282730	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88701148	CATATTTCTACATTT[A/G]AAAACAGGGTGATTT	161436
rs545289795	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686004	ATATTAGTAAAGATG[A/G]TAGACTCAACTCATA	161436
rs545291178	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763439	AGACACACACACCCC[C/G]CCAAGACTAAACCAG	161436
rs545302889	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679162	TAGAGCCCAACCAAA[C/T]CTAGTATGCCTTTGT	161436
rs545322978	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88686474	CCGGAGGATGGTCGG[C/T]GGACAGGGAGTTGGG	161436
rs545336007	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88736283	GGATTACGGGCGTGA[C/G]CCACAGTGCCTGGCC	161436
rs545344583	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88699599	AATGGATAGAGGAAA[A/T]AAGCAGAAGACCAAT	161436
rs545353259	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88689571	TTCCTTCCTTCCTTC[A/C]TTCAAGAAATATATT	161436
rs545361045	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612777	TTGGCCTACTGTATT[A/G]CTTACAGAGTTTTTT	161436
rs545362601	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782460	GAGCCAAAGGCTAAT[C/T]ACAAAGACAAAGAGG	161436
rs545385085	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88648825	TTCTGGTAAAATAGT[A/G]TAAGATTTTATGGCC	161436
rs545397071	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88656161	TACTATAAAGACACA[C/T]GCACATGTATATTTA	161436
rs545404488	snp	C/T	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88756505	TCTAGCCAAGAAAAA[C/T]AGGCCAGGAAAAGGA	161436
rs545416866	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88744679	GCAAACAAGCAAAAA[C/T]CCAGGTGAAATAAAA	161436
rs545418738	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640805	AAACAAGATCAATAG[A/G]CCACTAGTAGTTAGC	161436
rs545441115	snp	C/T	0.000231435	0.0107547	intron-variant	EML5	GRCh38.p7	14:88696976	GAATTATAGAAGCTA[C/T]TAAATACAATTAAAT	161436
rs545450020	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88745457	TGGCTATGATGTATT[A/G]TTTATATACAATTTG	161436
rs545451291	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761791	TCTTCCACAATGGTT[A/G]AACGAATTTACACTC	161436
rs545464287	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88781063	GTCTATTATAAAAGA[C/T]TCAGTTTCCCTAAAC	161436
rs545464984	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652461	ATAAAATCCATAGGT[C/G]CAAACTCAAATCCCT	161436
rs545480122	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645556	AATATTTCTATGAAC[A/G]TTCCACACTGTTAGC	161436
rs545486586	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88751957	TAATAGCATCTATTC[A/C]AAAGGGTTGTTGGGA	161436
rs545512394	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88748380	GAACTCGCTGGGCAG[G/T]CATTAGGAATCCTGA	161436
rs545523263	in-del	-/A	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88693752	ACTTCAGTTTCTACT[-/A]ATGTTAACATCTTTT	161436
rs545569129	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730557	AATATTGGGAACACT[A/G]CCAATAATTAATTTA	161436
rs545572473	snp	G/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774839	ATCTATACCAGCTCA[G/T]ATTGCTTCCCTGAAT	161436
rs545575633	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704032	CTCATCAGAACCTTG[A/T]AAGGTAGGTACTTGA	161436
rs545640021	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737107	ACTTCTTTCTTCTTG[C/G]ATGTGGGACAAGAAC	161436
rs545711225	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88699289	TTCTATCTATCTCAG[A/C]AGGCAAAAAAATAGT	161436
rs545728986	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779518	CTCTGTCATCTTTAG[A/G]AGGTGACCAATTACC	161436
rs545744009	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627497	TTAAAGTGAAATATA[C/T]CTACAGTACCACTGT	161436
rs545748175	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88702707	ATATACAGGGGAGAA[C/G]TAGGTACCCTTTGGG	161436
rs545752366	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641889	GAGTTTACACATACA[C/T]TCCTTTCTTGTTTAT	161436
rs545794118	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645176	AACAACAAGCGTGCA[C/T]CACCACACTCAGCTA	161436
rs545807263	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626730	ACCAGGGCATGTAAT[A/G]ATTAGCAGATCACAG	161436
rs545809731	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740666	ATATTAGAGCAGTGA[A/G]CTAAAAATTAACTAA	161436
rs545813977	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637840	GAAGCTAGACCTATG[C/T]ATTTATATGCAAAGA	161436
rs545815605	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88636648	CCTGGGCAACAGAAC[A/G]AGACTCTGTCACAAA	161436
rs545846208	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740190	ACAAGATACTAATTA[C/T]ACTAATGTAATAAAT	161436
rs545850795	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738693	CTCCTAACAATGAAC[C/G]TAAACTCTTTACAGG	161436
rs545851397	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747761	AATACAAGATTAGCA[A/G]GAGATGAAAAGACAA	161436
rs545877370	in-del	-/AG	0.115034	0.210438	intron-variant	EML5	GRCh38.p7	14:88775909	GGTGGCTCAGAAGAG[-/AG]AGAGAGAGAGAGAGA	161436
rs545916522	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703238	AAAACAATTGCTTTT[C/T]ATAAGTAAAAGGTAT	161436
rs545928363	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635845	CAATGAGATTAGTGT[C/T]CTTATAAGAGACAGG	161436
rs545937343	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88731147	CATATGTATACATGC[A/G]CCATGTTGGTGTGCT	161436
rs545961298	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88719372	GCCTGGGCAACAGAG[C/T]GAGACCTTGTCTCAA	161436
rs545965720	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659858	CTAAAAATATTAATA[G/T]GAGCAGTTACTCAAG	161436
rs545972686	snp	A/G	5.11043e-05	0.00505465	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622582	TTTCTGCTGCACTGT[A/G]TCAGCTCATGGAACA	161436
rs545974297	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681037	GGGTAGTTAAGATTA[A/C]AGATAGAAAAGAGTA	161436
rs545976405	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88672583	AGAGACACGAAAAGC[A/G]CGTCAAAAAATATTA	161436
rs546003110	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88784276	AAATCCAAAATTAGT[A/G]GAAAGAAATAAGATC	161436
rs546007947	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675668	ATTTATGCAAACTTC[C/T]GCAGCTGGCTTGAAT	161436
rs546020841	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88764900	CAATTCTTTTAAATT[C/T]GTTAAGGTTTGTTTT	161436
rs546059727	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771563	TCATCCCATTTCTCT[A/G]CTCCTCATTCAAAGC	161436
rs546064098	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726557	TTACTCTAAGTACAG[C/T]GAATGAGCCATCCTT	161436
rs546064927	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772475	TGTAAGATATACCTT[C/T]GGCCGGACGAGGTAG	161436
rs546065224	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778832	TTTCAGGGATCAATA[A/C]TGCAGTTTATCAAAG	161436
rs546074989	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88683852	CCACAGTTAACCTTA[C/T]ACTCAATGGTGGAAG	161436
rs546104946	in-del	-/TAGA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88759066	TAAATATTCTGAAAT[-/TAGA]TAGAAGTGATGGTTG	161436
rs546111975	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88728976	TTAAAATTGTTACTA[G/T]TTTATAGGAAAAATG	161436
rs546122036	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667375	GTTAAAAGAATATAA[A/G]ACCGTGACTAAATTT	161436
rs546134502	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674487	AAAACCATCAGATGT[C/T]GTGAGACTCACTATC	161436
rs546139157	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741738	AATAAACCAAAAAAA[C/T]GGGACAGGGCAGAGA	161436
rs546200186	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731610	GGCTGAGTGGAATGG[C/T]ATTTCTAGTTCTAGA	161436
rs546223694	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726131	GAAGAGATGGAAGCA[C/T]TTTTTAAAGCATAAG	161436
rs546249709	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681724	TAAAGCCAAGACTGA[A/G]TACAATTACGTTTCT	161436
rs546277351	in-del	-/TCT			intron-variant	EML5	GRCh38.p7	14:88632408	CATATCACTCCCTTG[-/TCT]AAAATTCTCCAGTGA	161436
rs546301064	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688621	TACAGGTGTCTCAAT[C/G]AGTGATGTGGGTAAC	161436
rs546303287	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615423	ACCTTGAAAATAAAA[C/T]ATAAACATTAAGAAA	161436
rs546344418	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88769593	ACTTGTAAAATACTG[A/C]GGTAACAAATAGTCA	161436
rs546365684	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648417	AGAGTGCAGTGGTGT[G/T]ATCATGGCTTACTTG	161436
rs546366571	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668990	ATCCAGGTTCTCTCA[C/T]TGGGACTGACAAGGT	161436
rs546394653	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710797	TACTTATGTCCTTGA[A/G]GGAGTGAATAATCTC	161436
rs546425767	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718138	CTAGGATACGGCCCA[C/T]AGACAGATGATCAGT	161436
rs546433032	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647324	AGCCAAGACTGCATG[C/T]GCCACTGCACTGCAG	161436
rs546445556	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655137	ACTACTGTAAATTTC[A/C]TATGAAACTAAAAAA	161436
rs546453008	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612296	TTTGAAAAGCATGAT[C/T]ATACAGGCCTCTCAG	161436
rs546457306	in-del	-/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768593	TTTTTTGTATTTTTA[-/G]TACAGACGGGGTTCC	161436
rs546471091	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88775970	TGAGTAAGAGTGTGC[A/C]TGCCTGGTAATCCAG	161436
rs546494051	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673490	GATGCCTTCTCTCAC[C/T]ACTCCTATTCAACAT	161436
rs546500654	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88760559	CCACACTGCCTTCAT[A/G]AGTATAGCTTTATTA	161436
rs546537085	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, synonymous-codon	EML5	GRCh38.p7	14:88616075	AACCAAAGCTGTAGG[A/T]GTTGTTGTATTAAGT	161436
rs546578073	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88721190	AAATTGCCATCCTGC[C/T]CAAAGTAATTTATAG	161436
rs546579813	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88733035	TAATGTGAAACTTAC[A/C]TTGTGGTAAAGTCAT	161436
rs546651142	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697340	ACAAACACCTCTTAA[C/T]AGATGCTTAATGAAC	161436
rs546712002	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749279	TAGAAGACAATGGAC[A/C]AACAGTTTAAAGTGC	161436
rs546736691	in-del	-/T	0.124144	0.21601	intron-variant	EML5	GRCh38.p7	14:88693938	ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT	161436
rs546750174	in-del	-/A	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613418	GATAGTTTTGTTCTC[-/A]AGTTTCACTATAAAT	161436
rs546751663	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88617525	AGTAATCCCAACATT[G/T]TGGGAGGCTGAGGCA	161436
rs546788304	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88622862	AATATTCTTGTAAAC[C/T]TTCTATGGCAATTTG	161436
rs546807162	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735430	TGAACAGGTCAAAGA[A/G]AAAAATGTCCTCTAA	161436
rs546808681	snp	A/C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734609	AAATACTAATCTAGA[A/C/T]GATAATCATCAATGG	161436
rs546813932	in-del	-/TGAT	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88789531	GAACCAGTAAGCAAA[-/TGAT]TGATAGACTAGTCAT	161436
rs546836777	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779908	TTTTACTTCTATGTT[A/T]CTGTGAGGAAATAAT	161436
rs546843626	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88733731	CTGATTAGCATACCA[C/T]AAAAAACATCAGTAA	161436
rs546886893	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751870	CAGACAAAATCTTAT[C/T]TGTGTCCATTAACTG	161436
rs546887239	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662482	CTATTTGCTATTTCA[C/T]GCTTCTTGTCTTTTA	161436
rs546888711	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88620614	AGTATACAAACAGCC[A/G]TATTTTAGCATACAA	161436
rs546923562	snp	C/G/T			intron-variant	EML5	GRCh38.p7	14:88715660	ATTACTTCAGTAATA[C/G/T]TTTTTTTTTTTTTTT	161436
rs546934513	in-del	-/AAAAAG	0.0162398	0.0886349	intron-variant	EML5	GRCh38.p7	14:88660763	AAAAAAGAAAAAAGA[-/AAAAAG]AAAAAAAAACTTAAT	161436
rs546943104	snp	C/G	4.44415e-05	0.00471368	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638844	ATGTTGATAAATTTG[C/G]GGTGCTGGTTTACTG	161436
rs547066704	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652569	TTCGCTTGAATTTTC[C/T]ACAAATCCTGTTCAA	161436
rs547071034	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660440	ATTAGCATAGGTACG[C/G/T]AGAATGCCAAAGAAT	161436
rs547080401	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757432	TTCTCAGATATAACA[C/T]AAAGCATTAGTGACA	161436
rs547116603	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708422	TCTTTAAAGACAGCA[A/G]TGGTGTCTTGTTTAA	161436
rs547119446	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703559	TCATAAAATACAACT[A/G]CATAGAAACTACTGC	161436
rs547122059	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765722	CCAGTCTGGCTACCA[C/T]GCAGACTCAGAAATT	161436
rs547133948	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88676170	TCTTTTCAGCAGCAT[C/G]CCACTCTACTGGTAC	161436
rs547149788	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88745045	TGTCATATTTTGTAA[C/T]GGGTCTATTTATATA	161436
rs547179418	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88684217	TTTATAACAGCATCA[A/G]AAATAATGGAAGTTA	161436
rs547185701	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88619115	TCACACCTATAATCC[C/T]AGAACTTTGGGAAGC	161436
rs547185976	snp	A/G	9.97026e-05	0.00705984	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626856	ACCAAATGCAATAGC[A/G]AGCATGGTCTGCATC	161436
rs547188256	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753579	GAACAACCTGCAAGA[C/T]CCAACTTTTTACTGG	161436
rs547190854	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727263	CACCATATGGTAATG[C/T]ACATAGCGGTCAAAA	161436
rs547192419	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88746418	CCTATATTTTATAGA[A/C]CTCATAAAGGCTGAA	161436
rs547198700	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88670543	CACCTCTCCAGCAAG[C/G]GCACAGAACTGGGCA	161436
rs547204220	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731189	CTCGTCATTTACATT[A/G]GGTATATCTCCTAAT	161436
rs547267655	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779165	GAAAAATATACCTTC[A/G]TTATTAAGCAATCCA	161436
rs547277926	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785522	AGCTGTTGATCTTTC[C/G]TTCTGTCCAAAATAT	161436
rs547285153	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636390	GCAAAAGGCTGGGCA[C/T]GGTGGCTCATGCCTG	161436
rs547286687	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88724152	TGGTGGCACGCACCT[A/G]TAGTCCCAGCTACTC	161436
rs547320888	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88693852	CACAGCTCACTGCAG[C/T]CTTAACCTCCTGGGC	161436
rs547349195	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643414	ATTTAAAACACAATA[C/T]TGTATAACAAATATG	161436
rs547367607	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775716	GAAGCACACTGGCCT[A/G]GCCGGCTTTACCACC	161436
rs547376672	in-del	-/A	0.207559	0.246371	intron-variant	EML5	GRCh38.p7	14:88682408	TAGTAAAAATCAATT[-/A]AAAAAAAAAAAACGC	161436
rs547384412	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792230	GCAGGAGCGGTCACG[A/G]CGTCCAGAGGAACCC	161436
rs547441113	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88754449	ATATTTATAGATTTA[C/T]AATCATTTTCTATAA	161436
rs547493199	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88743385	CCCATGAATATGTAC[A/T]ATCATTATTTGTCAA	161436
rs547517144	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790085	GAACTGAAAAAATAT[G/T]GAGGTTTTAATATTA	161436
rs547530731	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673059	AGCATGATCTTGATA[C/T]CAAAACCTGGCAGAG	161436
rs547532841	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656907	AAGTTAGCAAATAAG[A/G]TGAATCATATCAACC	161436
rs547542139	in-del	-/C	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88738318	CCCAAGGTCACACAA[-/C]TTGTAGGTGACTGGA	161436
rs547544342	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724925	CAAATTATAACAGTA[G/T]GGATAGCCCAACAGG	161436
rs547637988	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88635282	ACCATAGTGCCTTGA[C/T]CTGGAACATGAGGAA	161436
rs547642434	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88645890	TATTTATAATGTGCC[A/G]TGTCCCAACAGGTAT	161436
rs547648139	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672610	ATTAATGAATCCAGG[A/G]GCCGGTTTTTGAAAA	161436
rs547670754	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711647	ATGAGATTTGGCTGG[A/G]GACACAAAGCTAAAC	161436
rs547705206	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784397	GATTGACAAACCTTT[A/G]GCCACATTAAGAAAA	161436
rs547719000	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88708924	CAAGACAAACTATAA[C/T]GATCATAGAAGCTTC	161436
rs547728608	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88782792	GAGAATGTATGAAAA[C/T]GCCTGGATCGGGCAC	161436
rs547742025	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88783632	AATTTTAAATATATA[C/T]GCACCCAACACTAGA	161436
rs547743896	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793113	CAAGTGCGCGGGCCG[A/G]TGAGCCCTCCCTCGT	161436
rs547763734	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88663570	TATGCCATGCATTCT[G/T]CTAAAATACAAACAT	161436
rs547808999	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88782263	AGAGATCTGTGGAAC[A/T]TTGAACTTAAGAGAG	161436
rs547814719	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714475	ATCTAATATACAGCT[C/T]GTTGAGTACAGTTAA	161436
rs547816506	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88675179	ATAACTCCACTAGGC[A/G]GTGCCCCAGTAGGGA	161436
rs547834104	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640935	ATGAACACCTCTAAA[C/T]ACACAAACTAGAAGA	161436
rs547841273	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88631191	GTGTCCACTGAAAAC[A/G]TATCTAATGTATTCA	161436
rs547841314	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772621	AGCAAGGCGTGGTGG[C/T]GCGTGCCTGTAATCC	161436
rs547881818	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629167	TATATGTTTACAAAA[A/T]GCACCTCTAGGCAAT	161436
rs547903316	in-del	-/AAAT	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88755119	GGTAATTTGGATTTA[-/AAAT]AAATAGCTTCTATAA	161436
rs547946159	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638003	TATCAACTTAGTACT[C/T]GCATGAAAAATAAAG	161436
rs547950668	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704509	TTACAGACAGAAAAA[A/G]AGAGACACAGAGAGG	161436
rs547970483	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715134	AAGTTCCATCTGGTG[A/G]ATATTTTAACTCATG	161436
rs547994415	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689665	CTTGAGCCTGAGAGG[C/T]AGAGGTTGCAGTGAG	161436
rs547996839	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664407	TCTTTTTAACTCATC[C/T]GTTGAATCACTTTTC	161436
rs548026806	in-del	-/AATTC	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88685472	CTTATTAGTAATTTT[-/AATTC]AATTCAAGATATATA	161436
rs548035188	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727218	CTTATGTCAACATGA[C/T]GAGTATGCACTGGTG	161436
rs548056830	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762236	AAGACACGGGCCATG[C/T]GTAGTGGCTCACACC	161436
rs548085426	in-del	-/AAGAAATTCTAGAAA	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88748250	TGAGGTCATGCAAAG[-/AAGAAATTCTAGAAA]AAGAACAATTACTAG	161436
rs548090043	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774857	TGCTTCCCTGAATTA[C/T]AGACATGTATGTTCA	161436
rs548095100	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768441	TTTGAGACAGAGTTT[C/T]GCTCTGTCACCCAGG	161436
rs548107484	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738839	AATCTTTGGGAAGTT[A/T]AGAGTTTGCCTAGTA	161436
rs548121365	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772174	TCTTTTCCTCACTCA[C/T]CTCATGCATTCTATT	161436
rs548131361	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767587	GTTCTTAATATATTC[C/T]TGGTACAATTCTTTT	161436
rs548132778	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660615	GGGCATGGTGGTGCG[C/T]GCCTGTAATCCCAGC	161436
rs548135100	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88640874	AATGACAAAGATCAC[A/G]TTACAACCAATCCCA	161436
rs548144948	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617338	TTTTAGTAGAGACAG[G/T]GTTTCTCCATGTTGG	161436
rs548144981	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625423	TTATTTTTTTGAGAC[A/G]GAGTTTCGCTCTTTG	161436
rs548174818	in-del	-/AAC			intron-variant	EML5	GRCh38.p7	14:88726440	GGATAAATAGGTAAA[-/AAC]AACAAGTATTATATA	161436
rs548223660	snp	A/T	9.24428e-05	0.006798	intron-variant	EML5	GRCh38.p7	14:88726701	ATTTAATTTAAAAAA[A/T]AAAAAAGGTTAGCTA	161436
rs548236403	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628217	ACCAAGTATACATTC[A/G]GTACTGATGTTATCT	161436
rs548244206	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763012	ACAGCTAAAGAAGTG[C/T]TTAGAGAGAAATTTA	161436
rs548253473	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88763741	TCCCTGATGAACATC[A/G]ATGCAAAAATACTCA	161436
rs548260818	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778187	ATATCACCAGAGAAC[A/G]TCACCTTAACTAAAA	161436
rs548309571	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88619628	AAGAACACAGCCCAG[A/C]TTAACTAACCTCCAG	161436
rs548319238	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666684	ATGATGTTAACATTC[A/G]TAAAAATAAGGGTTA	161436
rs548353293	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645210	TGTGTATTTTTAGTA[A/G]AGATGGGGTTTCGCC	161436
rs548377991	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770823	TGAGGGTATATTCCC[A/T]TTCTAAAACATTTAA	161436
rs548387511	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653361	GTGAGAGACAGCATC[C/T]TTGTCTTGTGCCGGT	161436
rs548415436	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644932	GGCCAGGCTGGTCTC[A/G]ATCTCCTGACCTCAG	161436
rs548446153	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696276	ATATAGAATTCTCTA[A/T]TAATGTATTTCCTCC	161436
rs548486811	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667825	CTCTAACAATTTAGC[A/T]GCAATTTGCGGACTT	161436
rs548526734	snp	G/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793850	TTACTCTTAATTAAA[G/T]AAATTCAATTGTGAT	161436
rs548560310	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88709958	GAATCTAAATGATAT[G/T]TTCTCCAAATATAAA	161436
rs548564785	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710176	AGAGCAGGTGAAACT[A/G]GAGAAAAAGAGGATG	161436
rs548608757	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761343	TCTCCTAATGCTATC[C/T]CTCCCCTTGCACCCC	161436
rs548616666	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659178	AAGGTGTTAAAATGA[C/G]AGATGTCTTATACAA	161436
rs548623027	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88624719	TTAAGAAAAGTAACT[C/T]AACTTGTAGGACAAC	161436
rs548623538	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666237	CTTTATAAAAGTAAT[C/T]TTTTTTGAGATGGAA	161436
rs548669576	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88662426	TGGATTCCTAAGGAC[A/G]TGGCAGATATGCAAT	161436
rs548678060	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770192	CTATGGTTTGCACAG[A/C]AAGTCTGGAGAAGAG	161436
rs548701887	snp	A/C	4.98542e-05	0.00499245	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616165	ATCACCTCCAGCACT[A/C]ACAACATGTCGATCA	161436
rs548723185	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88672966	CAGAGGTACAAAGAG[A/G]AGCTGGTACCATTTC	161436
rs548733424	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88627459	ATTTATCTGTTTTGT[A/G]AGGTTACAGTTCCAC	161436
rs548744159	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637270	AGCTACATATATAAT[C/T]TAAAATTTACCTCTG	161436
rs548754196	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790430	TTCCTTACAGTTTAC[C/T]GAAACACAATTATGA	161436
rs548760979	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642290	AGTAGCATTATCACA[C/T]TGTTCATGAAATGAT	161436
rs548763517	snp	C/T			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613547	CACTGCCCAGACACA[C/T]ATTTAAGAGTTTAAT	161436
rs548765286	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88662629	CTCACTGCAGCCTCC[A/G]CCTCCTAGGTTCAAG	161436
rs548788856	snp	A/C	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88732219	ACATGTAAGTCTTTA[A/C]TCCATCTTGAATTAA	161436
rs548789459	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88739383	AGACTTGAGTATGTG[C/T]AGATTTTGGTATCTG	161436
rs548818339	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766967	TTCTTTCATAAATTC[A/C]ACATGTAGGTCATCC	161436
rs548837320	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648530	TGCTAATTTTTAAAA[C/T]TTTTTTTGTAGAGAC	161436
rs548838054	snp	C/T	0.0154538	0.0865337	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626576	GAGCTATAATCGCAC[C/T]ATTGCACCCCAGCCC	161436
rs548838513	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88747272	CAAAAATTAGCCAGG[C/T]GTGGTGACTCACGCC	161436
rs548872636	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88765031	TCCTTTGTCTCTAAC[A/C]TAGGAATTTCACGTC	161436
rs548900246	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88633141	GCCCCCAGATCATGC[C/T]TCAGCTATCTACTCC	161436
rs548908430	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88790343	ATGTATATTCAACGA[C/T]GAGAAATTCGAGTAT	161436
rs548909143	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88731285	CCAAGTGTTCTCATT[G/T]TTCAATTCCCACCTA	161436
rs548930375	snp	C/G	1.80409e-05	0.00300336	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706377	ATCATGTGACCATCT[C/G]ACATTAGTTACGTGA	161436
rs548946770	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655600	AACACTGACAGCAAT[G/T]GCAACAAAAGCAAAA	161436
rs548953941	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88636906	CAGGGTTCAAACACA[C/G]TGTAACAGAGAGGAC	161436
rs548967478	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714264	CAGTGGTACTTTACC[A/G]TACACTATACTCATG	161436
rs549012171	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88663449	ACTTTATGATGCTCA[A/G]TTTATATAGTTGAAT	161436
rs549038710	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767495	ATCATATACTTCCCA[C/T]AACTGGGCCTGCCTC	161436
rs549058490	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88697952	ATGTTGGTCAGGCTG[C/G]TCTCAAACTCCCGAC	161436
rs549061268	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690935	TGTTTTTGTACAATG[C/T]CCACTAGAGCAGGTT	161436
rs549087925	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88696320	ACACCCTAGCTTTCA[C/T]CGTAGATCTATCTGT	161436
rs549092720	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640080	CCATGAATACTACTA[A/G]GCCCCCCAAAAAGCA	161436
rs549095655	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705031	ATATACTAATAAAGG[G/T]GTTCGTATACTCCCA	161436
rs549146914	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88741748	AAAAATGGGACAGGG[A/C]AGAGATACATACATT	161436
rs549160870	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615474	TGAAAATTATCCAAA[C/T]TGGGTTTTTGAGTTC	161436
rs549172994	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623416	CAAATGCTATGCTAC[A/G]GAGTTGATTTATTTA	161436
rs549186430	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88744957	TCACCATAATACAGA[C/T]TATATGAAAAACATA	161436
rs549217954	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728093	TTTAAATGCATATAC[A/C]GTTGGCCCTCTGTAT	161436
rs549227521	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88675832	TTAGAAATTTCTTCT[A/G]CTAGATACCCTAAAT	161436
rs549255203	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88652973	GTCCTCTCCTATTTC[A/C]TTGAGCAGTGGTTTG	161436
rs549257028	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613951	ATATGACCTTTAGTC[A/G]TGAAACTGACAGCAG	161436
rs549261582	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773732	TTTGTTTTCTTTTAA[C/G]TTTCTATTAAGCAGC	161436
rs549262592	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775268	GTCTTGTACCTTAGG[A/T]ACCAGCATGGCCATA	161436
rs549291009	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692399	AAAAAAGGATGGTTG[C/T]TCTGTACTGAATACA	161436
rs549295864	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617297	GGATCACAGGCATGC[A/G]CTAACATGCCCGGCT	161436
rs549366279	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639091	ATGTAATGGGATAGA[A/G]CCGTAAAAGGGATAA	161436
rs549380176	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631066	TACAAATACTACCAG[A/G]GAGTGAGTTTTCTCT	161436
rs549406263	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646328	TAAGCATGACTGGTG[A/T]CATAAAAAGTAAACA	161436
rs549421199	snp	A/T	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684238	ATGGAAGTTAAAAAC[A/T]CGGCTCACTGCAAGC	161436
rs549431743	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88740977	AGACCAGCCTGGCCA[A/G]TATGGCGAAGTCCCA	161436
rs549440563	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695141	GTTATATCCAATGCC[A/G]TATTATAGTTATATT	161436
rs549442209	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714793	AATATATTGTATTAT[A/G]TTGTAGAAAAGTCTA	161436
rs549447773	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88751525	TTTTTTGTTTGTTGG[-/T]TTTTTTTTTGATAGT	161436
rs549456491	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88749412	ATGAATCATCAGTAA[A/G]CCTGCACTACAAGAT	161436
rs549469991	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645942	ACTTAAATGTAGAAG[C/T]TCTTCTCTAGAACCT	161436
rs549493763	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701407	GACACTGTATCACAA[C/T]TCAGAATGTGAGTTT	161436
rs549516140	in-del	-/CTC			intron-variant	EML5	GRCh38.p7	14:88667281	CTATTTGACTTTTCT[-/CTC]CTTTTTCTCCTTCAT	161436
rs549548397	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623831	GCAGGAGTAAATGAC[A/G]TGGGAAATACAAGTG	161436
rs549550804	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717750	ACAGGGCGAGACTCC[A/G]TCTCAAAACAACAAC	161436
rs549568875	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720557	ATAGGTGCAGAAAAC[A/G]CCTTTGATAAAATTC	161436
rs549581855	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88650910	GCCTCCCAAAGCACT[A/G]AGATTGCAGGCATGA	161436
rs549587584	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88725849	GAGCTATCTCAGAAG[G/T]AGACTCTCCAGAACT	161436
rs549589548	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88717263	AAAGAGCTGATGGCA[A/G]GAGAAAGTATTCAAG	161436
rs549592298	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88687670	GAGAAAACAAAAATG[G/T]TAACTACCTGATGGA	161436
rs549597173	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793505	CAGTCTCCGGAGTAG[C/T]AAGGAGTACAGTTGC	161436
rs549624962	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88784775	AACCACTATGGAGAA[C/T]AGTTTGGAGGTTCCT	161436
rs549626551	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88725134	AGAAAGTAGAATGAT[G/T]GTTATCATGGGCTTA	161436
rs549635475	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669134	TGTGCTATCCTGCCC[A/G]GGAAACCACACTTTT	161436
rs549640113	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773299	AGGATATCTGTCTTT[C/T]GGTGTTTTCAGCTCA	161436
rs549696912	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676915	ATTTGTTTGTTTGTA[C/T]TTTTTCTGAGACAGA	161436
rs549728932	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788650	CCAAGTTAATTATAT[G/T]CCATCAATGGTCTTC	161436
rs549729012	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779980	TTTGAAATGGAGTCT[C/T]GCTCTGTTGCCCAGG	161436
rs549750656	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793270	GAAAATCCACACCGG[A/G]ATGCTAAATTCTCTT	161436
rs549763313	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88636597	ACCCGGGAGGTGGGG[A/G]CTGCAGTGAGCCGAG	161436
rs549767135	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731867	CTGCATAAATGTCTT[A/C]TTTTGAGAAGTGTCT	161436
rs549770502	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88650772	CCTCCTGAGTAGGAA[C/T]CTCCTGGTACAGGCA	161436
rs549773989	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668048	ATGTTCTGGTGGCAG[C/T]CACACCATTTCCAAA	161436
rs549783502	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738290	CTTATTTACAGTGAG[A/G]GTAAATTACCAGCCC	161436
rs549787659	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727224	TCAACATGATGAGTA[C/T]GCACTGGTGATAAAT	161436
rs549794770	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88671761	GCAATCCTAGTTTCT[A/G]ACAAAACAGATTTTA	161436
rs549812214	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635402	TGAGAGGGCTTGGAA[C/T]TTTGCCACCTGAAGC	161436
rs549826060	in-del	-/G	0.0281293	0.11521	intron-variant	EML5	GRCh38.p7	14:88729569	TTGGTTTTTTGTTTT[-/G]TTGTTTTTTTGAGAC	161436
rs549838051	in-del	-/TCA			intron-variant	EML5	GRCh38.p7	14:88632992	GCTCCGGATTCCACC[-/TCA]TATGTCTTTTCCCTT	161436
rs549851651	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774992	CCCTAGCTACCAGAC[A/G]ACATTTTTATTCCCT	161436
rs549862753	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768544	GCCTCCTGAGTAGCT[A/G]GAATTACAGGTGCCC	161436
rs549862772	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88626039	CCAGGAATTGTGCTA[C/T]TTCCTTCTGTCTCAC	161436
rs549863933	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88768813	TATTTAACCCATCTA[C/T]TTATATCAGCTTGAA	161436
rs549903794	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770932	CCTATTAATATTGCT[A/G]AGTAATGGAAATTAA	161436
rs549940323	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88680122	ACTTATATTATGATT[C/T]TGTCTTTTTGTATTT	161436
rs549963430	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619827	CTGCCACCACGCCCG[A/G]CTGATTTTTGTATTT	161436
rs550015808	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678768	AAGCAAAACTAATAC[C/T]GTGAGAATAATTCTT	161436
rs550034743	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666353	TGCCTCAGGCTCCCA[A/G]GTAGCTGGGATTACA	161436
rs550036355	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88624740	GTAGGACAACTACCT[A/G]TCCACACCTCAGAAA	161436
rs550042113	in-del	-/TA			intron-variant	EML5	GRCh38.p7	14:88629152	TTATATAAATATTTT[-/TA]TATGTTTACAAAATG	161436
rs550072888	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709185	AAAATATCTTTCTGA[A/C]CCTAGTAAAAGTAAG	161436
rs550088062	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777425	CTGTCCTACAAGAAA[C/T]GCTAAAGGAAGCACT	161436
rs550093609	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673066	TCTTGATACCAAAAC[C/T]TGGCAGAGATGCAAC	161436
rs550114940	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773064	TCGGAGGTATCTGCA[C/G/T]GCCAGTGTTACAAGG	161436
rs550126309	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88776620	GCATGGTGGCTCACA[C/T]CTGTAATCCCAGCAC	161436
rs550132481	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636973	ATCCAGGAAAAAAGT[C/T]TGAATGTAACTGGCT	161436
rs550154691	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617801	ATTTTTCATTGGCCA[A/G]AAAAATGGATAGTCA	161436
rs550166658	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88625489	TCACCACAACCTCTG[C/T]TTCCCAGGTTCAAGT	161436
rs550169647	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656995	TAGGGTTTTGTTTTT[C/G]TGGGTATTTTTTTTT	161436
rs550171371	in-del	-/A	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88753333	TCATCTCACTACCAG[-/A]AAAATCACATTAACC	161436
rs550183671	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88723564	TAATAATAATGTAGA[A/T]TATACTTGAAAATTG	161436
rs550194679	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668361	GCAAAGGAAACAGAA[A/G]AAGGGAGTCAGTGAA	161436
rs550220305	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722937	AAAATGTTCATAAGA[A/G]CTAAGAAAACATGGT	161436
rs550230564	in-del	-/TCT			intron-variant, cds-indel	EML5	GRCh38.p7	14:88616299	ACAGAAGTCAAAGGC[-/TCT]TATTAGGAACTATAA	161436
rs550233670	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88780033	CGGCTCACTCTGTAA[A/C]CTCCACCTCCCAGGT	161436
rs550251934	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779742	TATCTTGAGGAATGA[A/C]TTTTAAGACCAGAGT	161436
rs550251981	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88772580	CAACGTGGTGAAACC[C/T]GTCTCTACTACAGAC	161436
rs550256613	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686268	CAGAAGTCAGAGAGA[A/G]TGTGGTGCTATGCCT	161436
rs550259072	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730103	TTGTTTACCAATGTA[C/T]ATATTAATACTGGAC	161436
rs550270399	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88782162	ACCCTGAGGTGGTCT[C/T]AGATGGAGAAGAGAA	161436
rs550281151	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634026	CAAGATACTTGATGA[C/T]ATGGTTTGGATATAT	161436
rs550288738	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779045	TCTCTTTTCTTCTGG[C/G]GCAAGCAACCATCAA	161436
rs550303671	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88725149	GGTTATCATGGGCTT[-/A]GGAGATGGAAGAATG	161436
rs550313392	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768498	TCGCTGCAACTTCCA[C/T]TTCCAGGGTTCAAGT	161436
rs550331146	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650210	GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGTGG	161436
rs550331849	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88697988	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	161436
rs550353570	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708489	ATTAGATATTTGAAG[A/G]AAGAGAAAAAGAAAG	161436
rs550394242	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657681	ATTATATGTAATGAT[A/G]TTTTCAAAGTATTAC	161436
rs550399865	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675884	TCCACAAATCTCCAG[G/T]GCTGAGGGAAAATGC	161436
rs550410466	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683564	ATATCTCTTATAAAT[A/G]CTGATGCTAAAATCC	161436
rs550425358	snp	A/G	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88763005	CTGGGACACAGCTAA[A/G]GAAGTGTTTAGAGAG	161436
rs550437123	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88630305	AAAGTGCTAGGATTA[C/T]AGGCATGAGCCACCA	161436
rs550468519	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88769405	TCCCCAGAAGCAGAA[A/G]CTGCTATGCTTCCTA	161436
rs550475446	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88772271	TCTTACATCACAACT[A/G]CTTCGGTAGCCTTCT	161436
rs550483368	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660707	TAGATCATGCCACTG[C/T]ACTCCAGCCTGGCGA	161436
rs550497202	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716057	AGGGAGAAAAGGTAG[C/G]GGGAAGTAAAAATTC	161436
rs550505202	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623222	GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTCAA	161436
rs550508399	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705086	AAACAACAGCTTTAA[C/T]AGTAGTCTTAAATGA	161436
rs550515392	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613856	CATAGGGCAGATTCT[A/G]TATGGCCTATCATGT	161436
rs550549546	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88653976	CCAGACTTTGTTATT[C/G]GTCTATTCAGGGATT	161436
rs550549722	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614768	CTAATCCACTAAAAA[A/G]AGGAATTCTAACTGA	161436
rs550581965	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759345	ACCTTCAAAAAGGGC[A/C]TATATTTACTACAAG	161436
rs550582356	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720377	ATCAATGCAAAAATC[C/G]TCAGTAAAATACTGG	161436
rs550640536	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756416	TTAATGATGAAAGCC[C/T]GAAAGCAATCCCACT	161436
rs550660721	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88707521	CAGGATACAATGATG[C/T]TTAGCTTCCTTTTGA	161436
rs550687632	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652519	TATCTCTCTGAGTTC[C/T]AAAATTCTTCAGCAC	161436
rs550701278	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612751	ACTGCAAGATAGATA[A/G]GATGAAACTTTTGGC	161436
rs550710225	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88718402	TTTGAGGACCTCTAA[C/T]ATTTACTTGCTGGGC	161436
rs550722970	snp	C/T	0.00145856	0.0269658	intron-variant	EML5	GRCh38.p7	14:88705615	AAAAATGAAATGTTA[C/T]TTGTTTAAAGAAGAT	161436
rs550737477	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655007	GGTCTTCTTGTTGCA[C/T]TGATCCCTTTACCAT	161436
rs550740369	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757181	CATACATTTGTGGTC[A/T]ACTGATTTCAACAAG	161436
rs550757474	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88638747	TTTTTTCCTTGGATA[C/T]TGAATTTATTTGAAC	161436
rs550772637	snp	G/T	0.0404589	0.136354	intron-variant	EML5	GRCh38.p7	14:88729569	TTTGGTTTTTTGTTT[G/T]TTGTTTTTTTGAGAC	161436
rs550773560	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645787	TCTTTCTCTTCCCTT[A/G]TTCTCACTATTTACT	161436
rs550777220	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88765043	AACCTAGGAATTTCA[C/T]GTCTTTGCCAGCATC	161436
rs550792308	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755229	TCCCTGCAATATATT[A/G]TGTGTAAACTTCTCA	161436
rs550792542	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760519	TTTTACACCATTAAC[A/C]TATGTATCTATCCTT	161436
rs550858860	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623646	CCCAAACTCCTGACC[C/T]CGTGATCCGCCCACC	161436
rs550859177	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787272	GTGCTATTCCTAGTA[C/T]ACATATGCTCATTGA	161436
rs550923046	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88751460	GTGCTAACTGGAAAG[C/T]GGCAAGAGACAAGGC	161436
rs550950005	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88654539	AATTCTGTTATTTAC[C/T]CAGTAGTAATTCAGG	161436
rs550962581	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702872	CGATCCTCCCACCTC[A/C]GCCCTCCAAGTAGCT	161436
rs550964074	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695676	CATCGCACCTGATCT[A/C]CTTTTCCCTTATCTA	161436
rs551001731	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88651930	ACTTGAAATATACCA[C/T]AAGTTAGGGATTATA	161436
rs551011524	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88659234	ATTCCCTAGGAATGA[C/T]GACTCTCTTTTTTTT	161436
rs551072949	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764319	GCAATTGTGTGGAAT[G/T]GGAATCATTTATTCT	161436
rs551079251	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88621062	ATTTAGAACTTCCAA[C/T]TTTTCTTTTTAGAAG	161436
rs551104886	snp	A/G	1.66663e-05	0.00288667	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714949	GTTACCTGGCATTCT[A/G]TAAAAAAGTCTTTTC	161436
rs551115254	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666948	GAGATGATGATGACC[A/T]GGAGCTGGGTGGCAG	161436
rs551122316	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682927	TGACCTCACTCTCAA[C/T]TCCAGAGCCCTGGTT	161436
rs551149685	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88625562	GCCAGCCACCACGCC[C/T]GGCTAATTTTTGTAT	161436
rs551150502	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88690350	GATACAAGGGAGGTC[A/G]AGGATGAAAGGAGTT	161436
rs551159332	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752322	AATGGCTTGAATTTC[A/G]TAACACCTTAAATAA	161436
rs551174139	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634182	ATCTGCTCGTTTAAA[C/T]GTGTAGTACCTCCCC	161436
rs551180249	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674138	GCCAGGCATGGTAGC[A/G]CATGTCTGTAATCTC	161436
rs551195057	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737433	TGTGGGATCCAGCCA[C/G]AGTATAAGCCAAGCG	161436
rs551210694	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88704500	ATCTCCATTTTACAG[A/T]CAGAAAAAAAGAGAC	161436
rs551216477	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636535	GCATGGTGGCGTGCA[C/T]CTGTAGTCCCAGCTA	161436
rs551227554	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740310	TAGAAACAATATACT[A/G]TATTACGCAGTCTAT	161436
rs551229950	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745483	ATTTGGAATGAGGAA[A/T]ATATATTCTAACAAG	161436
rs551231816	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736717	AGCCAAGCTACAAGT[C/T]TCAGATAAATCCATG	161436
rs551232517	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88786310	CATATATAAAAATTT[-/AC]ACACATATATAAAAT	161436
rs551242980	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762510	AGTGAAACTCCATCT[C/T]GGGGGAAAAAAAAAG	161436
rs551254033	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88786395	TGGGCAATTTTATCT[C/G]TTTGGTTCACTGCCA	161436
rs551268724	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88745023	CTTTCAAAAACTCCA[C/T]TGACAGTGTCATATT	161436
rs551289960	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689713	CGCTCCAGCCTGCGT[A/G]ACAGAGCAAAACCCT	161436
rs551328613	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696468	CTCTTTCTTTGCTAG[C/G]CTTTTACCCTAAACA	161436
rs551329953	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88684814	CATTAACAGAAAAAA[A/G]CAAATTTTTTCTGTA	161436
rs551341951	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649209	ATTTATTTTTACTTT[C/T]ATTTTTTGTAGAGAC	161436
rs551390343	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88772825	CCTTTTGTTCACTAC[A/G]CTCCAGCTACACTGG	161436
rs551435996	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762227	AAACTTACAAAGACA[C/T]GGGCCATGCGTAGTG	161436
rs551442382	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709652	CACTTTGGAAAATAT[G/T]TAGGTATTTTCTTAT	161436
rs551449012	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655736	TATCCATCTGACAAA[C/G]GGCTAATATCCAGAA	161436
rs551464984	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644848	CCCGAGTAGCTGGGA[C/T]TACAGGTGTGTGCCA	161436
rs551476789	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652539	TTCTTCAGCACTATC[C/T]TAAATGGCCACAAAT	161436
rs551478513	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729139	TTTTTTCCTTTCCAA[A/T]CTGTGTGTGTGTACG	161436
rs551518008	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768187	TATCAGAAGGTTTAG[A/G]GTGTCAATATTACTG	161436
rs551520538	in-del	-/AA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88664851	TGGGAAGCAAATGTC[-/AA]AAGCTATGTATGATG	161436
rs551548250	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730802	TGCTAAGATGAATTA[C/T]AACTAACTGATGGTG	161436
rs551577981	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88722059	CAAATCAAAACCACA[C/T]TGAGGTACCATCTCA	161436
rs551607839	snp	A/T	0.000644929	0.0179457	intron-variant	EML5	GRCh38.p7	14:88702410	CTCAAACAAAGGTGT[A/T]GCTTATCTGGCTTAT	161436
rs551616612	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721520	AAGCAAGGGGGAAAG[G/T]ATCTCCTATTCAATA	161436
rs551649428	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88684655	ACTGGGTTAAATTAA[C/T]TACAGCTGGTTTTTC	161436
rs551650548	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792131	CCCTAGACGAGGAAG[A/T]GGGGAAAGGCATTTG	161436
rs551670860	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88727849	TTTAAAACTATCCAA[A/C]TTCAGAATCTGTTCC	161436
rs551679349	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686319	AAGACGAGTTAACGG[A/G]TGCAGCACACCAACA	161436
rs551713542	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789883	TTGACCAATAAGTTT[A/T]ACATAAGTTTCAGGC	161436
rs551720992	snp	A/G	1.65811e-05	0.00287929	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88681972	ATCATCGCTTACAGT[A/G]GCACAGATGGGCAGA	161436
rs551734653	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693364	GGTGAATGAGGAGCA[A/G]AGTCACGTCTTACAT	161436
rs551748066	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735986	TAATAAAGTTTTAAT[C/T]GGAGTATTTTTTCTT	161436
rs551753918	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772248	ATCTTAATCTGAACC[A/G]GCATTCATCTTACAT	161436
rs551763733	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88793099	GGACCGCGTCTCTGC[A/G]AGTGCGCGGGCCGGT	161436
rs551798146	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631833	AGGTGTGAGCTACTG[C/T]GCCCAGCTCATATCT	161436
rs551808632	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640287	AAACATACTCTAAGA[C/T]TGACCACATGTTCAG	161436
rs551814218	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623954	TGAAAGCATGCCTAT[A/G]TGCATTCTTCCTTTA	161436
rs551853731	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688992	TTCTATAAATATCAT[C/T]CTGTATGTATTCTTT	161436
rs551876352	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742717	CCTTCACAGTGCTTA[C/T]ATCATGTGCCTTAAA	161436
rs551878086	in-del	-/AAATC	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88638714	TTTTGAACAATCGAT[-/AAATC]AATAAAATTTTGATT	161436
rs551880509	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639930	TGATTCATCTGGTAG[C/T]AGTAACAGTGAAGAG	161436
rs551883327	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88698523	TGCCGCCTCAGTTTT[C/T]GAAAGTGCTAGGATT	161436
rs551886048	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794370	GAAAGGAATTTACAT[A/C]GATGTCATGAAAAGT	161436
rs551888200	snp	A/C	0.000380892	0.013795	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688278	TTACTTACTTTTTCC[A/C]ATGCATGCATACTGA	161436
rs551903757	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617242	AACCTCTGCCTCCTG[C/G]GTTCAAGCAATTCTC	161436
rs551904360	in-del	-/A	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88685709	CCACCTGGGCCTCCC[-/A]AAAGTGTTGGGATTA	161436
rs551909039	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751398	GATTAGAGAGATCAT[A/G]GTGCTTTCAAGAGAG	161436
rs551917635	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88788489	AAATATTTCAGATGC[A/T]TCGTCATTTGAGCTC	161436
rs551950477	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644843	AGCCTCCCGAGTAGC[C/T]GGGATTACAGGTGTG	161436
rs551975825	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718649	AGCTGAAAGCAGAAG[A/G]CATATAGGAATGAGG	161436
rs552008202	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729567	TATTTGGTTTTTTGT[G/T]TTTTGTTTTTTTGAG	161436
rs552021956	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88695556	ATATTTAAAATTTGA[C/T]AAAATAATGTTAAAT	161436
rs552038165	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613683	AGGAAATGAGCATGG[C/T]TGGCGATTGGAAGCA	161436
rs552049924	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767562	GTCATAATATTGTTA[C/T]ACTGTAAGAGTTCTT	161436
rs552057657	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682683	AGCATTTCTCACCCT[A/G]CCCTCAGCCTCCTGT	161436
rs552075446	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781814	TTCCTGAGGCTTCTC[C/T]AGCCCTGCAGAACTG	161436
rs552088793	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774250	TTTTTTAGTAACTTT[C/T]CAGGTGATGCCGTTG	161436
rs552094008	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717823	GTAATAGGATCAAAA[A/C]CAATTAAAAGGTTAC	161436
rs552117953	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667753	CCTGATGGCATTCAC[C/T]AGAGTGGCAGCCCCA	161436
rs552136280	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733085	TGAATAACAATATCA[A/C]GCTGCTTTATACACT	161436
rs552137907	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632883	AGAAACACCTCATGT[A/G]TGTTGCTGGATTTGA	161436
rs552168081	snp	A/C	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88732040	CTCTGATGGTAGTTT[A/C]TTTTGCTGTGCAGAA	161436
rs552179638	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674942	ATCTTAAAGTTCCAG[C/T]GATCTCCTTTGACTC	161436
rs552183834	snp	A/G	0.000582009	0.0170489	intron-variant	EML5	GRCh38.p7	14:88665506	TGAAAGAGAAAGAGC[A/G]TATTAGGCAATTTTC	161436
rs552192870	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758515	CTATATTTTAAAAGA[C/T]AGAAAATATGAAGTA	161436
rs552196445	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768239	TGGTTAAACAGTACA[C/T]GCCACTGTAAAGATA	161436
rs552197355	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732566	CCTTTTTTGATTCCA[C/T]ATGAACTTTAGTTTT	161436
rs552240852	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619487	TGGGATTACAGGTGT[A/G]AGCCACAACACCCAG	161436
rs552243910	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785440	AAAACATCTCATGTA[A/C]CCCATAAATAGATAA	161436
rs552247035	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88721274	AAAACTACTTAAGAC[A/C]TCATATGGAACCAAA	161436
rs552248976	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88628454	TTGTGTAGCTTGTTT[C/T]TGCTGCTTAAAAAAT	161436
rs552277902	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775629	ACTTCTAAGGTTTTT[G/T]ACTCTAGTCCCTGAC	161436
rs552332846	snp	C/T	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88763114	TTAGAGAAACAAAAG[C/T]AAACAAATTCAAAAG	161436
rs552371256	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612861	AAATAACAGATCACT[A/G]ATTTCAAAGACTTGG	161436
rs552431668	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88662886	CCTTCACCCATGTAT[C/T]CTGACTCAATAAACT	161436
rs552435902	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667033	GAACTTTGACCAACT[A/G]GATGTGGGGTGAAAG	161436
rs552441503	in-del	-/TTGT	0.437255	0.165637	intron-variant	EML5	GRCh38.p7	14:88760347	GTAGGTTATAGTTGT[-/TTGT]TTGTTTGTTTGTTTT	161436
rs552445722	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88765134	TGTCACAAATTACCA[C/T]AAATTTAGCACCTTA	161436
rs552446879	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673984	TGCTATGAAGAAATA[C/T]CTGGCTGGGTGTGGT	161436
rs552474035	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88651706	TTCTAATTAGAATAT[A/T]TAAATAATATTATAT	161436
rs552481449	snp	G/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620917	CCAAATTCACTTTGT[G/T]TAACATCTTCTGCAT	161436
rs552481806	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772001	AACCCTGTATCTCTA[A/G]GTCAGCACAATGGAT	161436
rs552542665	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88629080	AATGTTAGGTGGCTT[A/G]AATTTAAAATGTAAA	161436
rs552553687	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618932	GGCCTCAAATAGATT[G/T]ACCTGTCAGACACAA	161436
rs552558861	in-del	-/T	0.0123036	0.0774623	intron-variant	EML5	GRCh38.p7	14:88654260	TGATTTTTTGAAGGG[-/T]TTTTTTGTGTCTCTC	161436
rs552589967	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88708677	AAAGAATATTAGAAT[G/T]GAAATCAAAAGACTA	161436
rs552600280	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723745	GTCAATCATGCCTTA[A/C]TGAAGCTGGGGGGAC	161436
rs552606220	in-del	-/T	0.274124	0.248833	intron-variant	EML5	GRCh38.p7	14:88758020	ACCACACCTGTCTAA[-/T]TTTTTTTTTTTTTTT	161436
rs552623708	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88716173	CAGTTGTATTTGAGT[C/T]ACTATACAGCTGTGG	161436
rs552639041	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660804	AGGAAGTAAATACCA[A/G]TTTTAAGCAGAAAAT	161436
rs552642804	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652944	GAGCATGGAATGTTT[C/T]TCCATTTGTTTGTGT	161436
rs552644270	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680341	AGAAACCTTTTTTTT[A/T]AAATGTGTCTGGCAA	161436
rs552644529	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88765366	GGACTGAGGCTTTCA[C/T]TCCCCTGCTGGCTGT	161436
rs552652946	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660211	TAACTTGGGTCTGGA[A/G]GGTCGATGCTGCAGT	161436
rs552657667	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697711	TAGAGCTGTCAATTA[C/T]AGTTAATTTTGAGAC	161436
rs552673320	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766121	AATCTCGTCATCTTC[A/G]TAAGCTGAGGATGTA	161436
rs552686201	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710534	TACTGCCAACTTCAA[A/G]GTATGTAATTATGTG	161436
rs552709988	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694760	TCCAACTACAAAATT[C/T]CTCTTAAACTATTGT	161436
rs552724588	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88684267	GCTCCGCCTCCCGGG[G/T]TCACGCCATTCTCCT	161436
rs552741530	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749778	CTCTGACAAAAACAG[A/G]ATTAGAGTAACAGAA	161436
rs552836131	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746777	AGGTGGGGATTTGAA[C/T]TGCAGACCGCCTCTG	161436
rs552858021	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780327	TGGAGGATATTTGTA[C/G/T]AGCAAACAGACTTGA	161436
rs552885185	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88735057	TTTAAAGATACAAAC[-/AG]AAATATTTACAGATG	161436
rs552921842	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88738138	TTTAAAGCACAATAA[C/T]GTTTAGCAAAACTAA	161436
rs552922066	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88634975	CCTTCTGAGCTGAGA[C/G]ACATGATGGCAAAGC	161436
rs552927075	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628721	CAGAAATAAATGTTG[G/T]TCTCTAAAGAAAATA	161436
rs552941291	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732958	AATTAGCTTCTACTG[A/G]AGACTCAATACTGTT	161436
rs552945893	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88639293	GAGGAACACTTTAAG[C/T]AGAGGCCTAAAGGCA	161436
rs553007540	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704761	ATCCTTTCGGATATG[A/T]CATTTCAGGGGATAC	161436
rs553011213	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88646032	ACTGAATAACCGGAA[C/T]ATTGAATTTAAATCA	161436
rs553016691	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88739794	AAACCAATTCAACAA[C/T]CACAAAAAATTTAAA	161436
rs553019288	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690598	AACTGCAAATTGAAA[C/G]TAGGAACAACTGTTT	161436
rs553035007	snp	A/C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668401	AGAAACAGACACGCA[A/C/T]GGGTTCCAGAGACAA	161436
rs553057193	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757968	ACTCATCCTCCTGCT[C/T]TGGCCTCTCAAGTAG	161436
rs553109743	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88744922	AGAAAGAATACATAT[C/T]ACAGTTAATATTTAA	161436
rs553111154	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772636	TGCGTGCCTGTAATC[C/T]CAGCTACTGGGGAGG	161436
rs553142536	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704068	TTCGGATATTTGTGC[C/T]GTCCAAATCCCATGC	161436
rs553144045	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645022	CACACCCAGCCTTTT[C/T]TCTTCTTTCTTTCTT	161436
rs553161944	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622166	TTCACTTCACATCAT[A/G]TCCTCCAGTCTCATC	161436
rs553173971	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640034	GGAAAATGAGTTCAG[A/G]GCAGTAGGTTGGATC	161436
rs553183341	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631292	GATCATGACACACCG[A/C]AGCCTCGAATTCCTG	161436
rs553188178	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646604	TATATAATCCTATAT[A/T]ACAATTAACCACATT	161436
rs553201420	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88747397	AGCCTGGGAGACAGA[A/G]AGAGACTCTGTCTCA	161436
rs553225733	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88777724	GCTCATGCCTGTAAT[C/G]CCGGCACTTTGGGAG	161436
rs553234818	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88748521	ATGAAACTGATTCAT[A/G]AGGAACTTGACTATT	161436
rs553246706	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88630685	TGCTTTGTGTCCTCA[C/T]GCAAAGTCAGGCTAA	161436
rs553249870	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772344	TCTCAACATAGCCAG[C/G]TGATCTTTAAAAATA	161436
rs553269335	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734133	AAGATCAACAACCCT[A/G]CAGAAAAAATGGCAA	161436
rs553302326	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88745223	CTCTGTGCACCTACT[A/G]AAAACCAAATGTATT	161436
rs553324955	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88726160	AGGCTGTAAATAACA[A/G]CAACAACAACAACAA	161436
rs553377346	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88689726	GTGACAGAGCAAAAC[C/T]CTGTCTCCAAACAAA	161436
rs553378833	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736921	TCCCCCATTCTGAGC[C/T]CATAAAGGCTCCAGA	161436
rs553413705	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736211	TCACTATGTTGGCCA[A/G]GATGGTCTCAATCCC	161436
rs553415926	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689315	TGCCAAACTGTTTTC[C/T]GAAGTTTATATACCA	161436
rs553422818	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88778552	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	161436
rs553437993	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88625981	AGATGAGATGGAATA[A/C]AGTGAGAGGAGAGCA	161436
rs553457370	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774660	CTCTTGGTTTTTCTC[A/G]TGTTTCTCTGGCCAC	161436
rs553467782	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88634340	GCCAATTAAACACAT[G/T]TTCTTTGTAAATTAC	161436
rs553470561	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88629541	AACTATGTTTATTAA[C/G]TATATTATATTTTCT	161436
rs553477939	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88722453	AAAGGAAGGAGATCA[C/T]GTCCTTTGCAGGGAC	161436
rs553487328	in-del	-/TC	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88654752	GAGAAGAATGTATAT[-/TC]TCTGTTGATTTGGGG	161436
rs553512866	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88719881	ATTAATAAAATAAAT[A/G]GACTGCTAGCTAGAC	161436
rs553522212	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652064	TGACTCCAGAATTCA[A/T]GTCCTTTGCACTATA	161436
rs553564176	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88780668	GCAACCTCCGCCTCC[C/G]AGATTCAGGCAATTC	161436
rs553579792	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88711444	TGAAGGGGAAGCAAG[A/G]CACCCTCTTCACAGG	161436
rs553607541	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765796	AAGTATTCCATTTTT[C/T]TACAACTTCTATTTC	161436
rs553619686	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617446	CCACCGCGCCTGACT[A/G]AAAACTGATAGAACT	161436
rs553620140	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88625697	GTGAGCCACTGTGCC[C/T]GGCCTGAGCCACGGT	161436
rs553740155	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682987	CCAGAAATCCAGATA[A/G]CTCCTAATCTCTTCT	161436
rs553745157	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767539	TTTTTCCTATTTTTA[A/G]ATTATTTGTCATAAT	161436
rs553767671	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713459	TCCATTCATGCACTC[A/G]CTCACTTGTTAATTT	161436
rs553786446	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641572	ATTAAAAACAAAAAC[C/T]ATATGATTATCTCAA	161436
rs553819030	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88667834	TTTAGCTGCAATTTG[C/T]GGACTTCAGGAAGAT	161436
rs553890649	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685876	TTACTTTTTATTTTT[C/G]TCTAGCATATTTTCT	161436
rs553912881	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792080	TGCCCGGTGGATCCG[C/T]GGACCTGATCTTCCT	161436
rs553913106	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662172	TAATAATGCATTATG[C/T]TTTCCAACTAACCCT	161436
rs553950541	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790655	CTGAATTCAACCTAA[C/G]AGACTAAATTATCTG	161436
rs553950881	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715761	CTCTGGGGATCAAGC[A/G]ATTCTCACCTCATAC	161436
rs553958681	in-del	-/AAAT	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614958	GTTTACATGTTAAAC[-/AAAT]GTGTATATATTAGAC	161436
rs553969201	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664866	AAAAGCTATGTATGA[C/T]GTAGTTTTGATACTT	161436
rs553972511	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669320	GTCATCACTTTGGCT[G/T]TCTGCTGCCTCAGAT	161436
rs554064111	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775153	AGTGAGCCTCTGAGG[C/T]TTGCTGGCTTCAGGT	161436
rs554082099	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705990	ATCTCTCAGAGGATA[C/T]ATTAAATGTTTGTTT	161436
rs554100756	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88669930	AGCCTCCACTGGTGA[C/T]ACCTCGAGGTGTGGG	161436
rs554108132	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743324	GATAGCTAATTACCC[C/T]AATCTGATCACCATA	161436
rs554134759	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780312	TTCTAGGCTATTTTT[C/T]GGAGGATATTTGTAT	161436
rs554135365	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616359	TAGGGAGTTAGCACC[A/G]CAGCCAGTGATTAGA	161436
rs554155782	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721553	TGGTGCTGGGAAAAC[G/T]GGCCAGCTATATGCG	161436
rs554156930	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751812	GAAAACCAGATAAAG[A/C]AGCCTCTATCCATCT	161436
rs554217729	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624008	TTGTGTTTAATTAAC[A/G]TATGTGGGTTCTTTC	161436
rs554238707	snp	A/C			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765503	TCTTTCTGACTTCTG[A/C]TGCATGTTTTCTCAT	161436
rs554241378	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674155	ATGTCTGTAATCTCA[A/G]CTACTCAGGAGGCTG	161436
rs554247018	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710305	TGAGCTAACTTCGTA[C/T]ATTTTTTGTTTCAAT	161436
rs554247737	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88705300	TACTTAATATACCAA[G/T]CATTTAATATAAAAA	161436
rs554255377	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88673225	CAGGATGCTAGGCTT[A/G]TTCAACACACACAAA	161436
rs554279274	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623548	CCTTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG	161436
rs554283518	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88717918	TACTCCATACTATTA[C/T]AGGACGTAATACGTA	161436
rs554297445	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	EML5	GRCh38.p7	14:88766767	TTTGCAGCTTGAGGG[A/G]CATCACGGAACCTGC	161436
rs554300414	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675095	GTGCCTGTGGCTTTT[C/T]CAGGCACATGGTGCA	161436
rs554351067	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717849	GTTACTGCAGATGAT[A/G]GTTTCTCAGACTTCA	161436
rs554398073	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777509	TGAAGGTACAAAACT[C/T]ACTGGTAATAGTAAG	161436
rs554436325	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647940	TAGCACTGGAGATAC[C/T]TCAAAGGAAATTGTC	161436
rs554454947	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88635678	GACAACCTGTCTCAT[C/T]CTCTTCCATCCCACA	161436
rs554460118	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88679017	GTGGTTGTAGCAATC[C/G]TTGGTGCTCCTTGGT	161436
rs554484453	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703103	TTTTATGAACTGCTC[A/G]GACTGCAAATAGCTA	161436
rs554491865	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637594	TTGCCTTTTTGTAAG[C/T]AGCCCATATCCCCAG	161436
rs554495944	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88655375	AAAAACAAGCAATGA[A/G]AAAGGATTCCCTCTT	161436
rs554516898	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88688038	ACCACACCACTGCGC[C/T]CCAGCTTGGGTGACA	161436
rs554521083	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88792760	ATGCCCAGAGCCCTT[C/T]GCCCGCCTCGGCTCG	161436
rs554564973	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709859	CATTAAAGCTACACG[A/C]AACAATATGGAAAAC	161436
rs554588894	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88650428	CACTGCACTCCAGCC[C/T]GGGCGACACAGCAAG	161436
rs554601791	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717338	GGACTTTGGTGTGAA[C/T]TCAGTCTGCTGAGGG	161436
rs554657892	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725985	GACTTCGTAAGTACT[C/T]ATCCTGTGGATCTAC	161436
rs554658295	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88763303	ATCAAATAGACACAA[C/T]AAAAAATGATAAAGA	161436
rs554660801	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88685615	CACATACATCATTCC[A/G]TATATTTTTTTTTTC	161436
rs554694312	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763910	GGGTTAAAGAAGTGG[A/G]CTTCTAGTCCTAGTT	161436
rs554715501	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681486	ACAAATGGGCTCAGT[A/T]CTATTTACAATATCC	161436
rs554724653	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657870	ATACATTTTCTATAA[C/T]GAGCTGATATTACTG	161436
rs554734159	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637715	ATGTACCAAGAGGCA[C/T]TGAGCTAGGTACTTA	161436
rs554748159	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784789	ACAGTTTGGAGGTTC[C/T]TCAAAAAACTAAAAA	161436
rs554787962	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665614	GGAGGACTGCCCGCG[G/T]CCAGGAGGTTAAGAC	161436
rs554797310	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644235	TATTCACAGAAAAGT[A/G]AAAGGAAGACTAATT	161436
rs554826172	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88747528	ACAAACAGCAAAGTC[A/G]GCCTTGCAAAAAACA	161436
rs554850010	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652734	TTTTGTTCTTTAAAC[C/T]TCTTTGCTTCTGAAG	161436
rs554850311	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660851	TGATGATTTAAAATG[C/T]ACATATATTCTGCTA	161436
rs554862116	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652290	ATACCATCAGCAAAC[A/G]ACACCTGGAAAAGGA	161436
rs554878738	snp	A/C	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88757726	ATGCTCAACATCAAT[A/C]GTCAGCAGGGAAATA	161436
rs554882046	snp	C/T	1.7399e-05	0.00294944	intron-variant	EML5	GRCh38.p7	14:88740590	AAAAGGTATATAGTA[C/T]AATCAAATTACCAAA	161436
rs554885123	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793553	AAATGTTTTGCTTTG[C/T]TTTTAAGTTTATTTT	161436
rs554889688	in-del	-/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88671243	AGTCAGGAGACACTA[-/G]GGGCCAATATTCAAC	161436
rs554908439	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636536	CATGGTGGCGTGCAC[C/T]TGTAGTCCCAGCTAC	161436
rs554910538	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617271	TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGATC	161436
rs554918431	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756631	GAGCTAATATGAATT[C/T]AGCAAGGTTGCAGGA	161436
rs554919970	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788330	AATAAGACTTGGTCA[A/G]TATTTTTTCTTAAGA	161436
rs554922574	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619168	GTCGAGAGTTTGAGA[C/T]CAGCCTGACCAACAT	161436
rs554926001	snp	G/T	0.029116	0.117091	intron-variant	EML5	GRCh38.p7	14:88640142	CAACCCACTGATAGT[G/T]TTAGATCATCAAGGT	161436
rs554927187	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738621	CCTAAGTGAGTACCT[C/T]TCACATCTCTCTATA	161436
rs554955477	snp	A/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688307	GAACACTGGCCCATC[A/T]TGCGCTTTCACTGTT	161436
rs554957092	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712210	CAAGACTAATTTTCT[A/G]CAAGAACACGAAAGT	161436
rs554957324	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660464	AAAGAATCTGTTGGC[A/G]AGGCCCAGTGGCTCA	161436
rs554971333	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88695580	GTTAAATGTTAGGCA[C/T]GCATACACCTATAAA	161436
rs554975670	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746883	AAACACCTCCCTGAA[A/C]ATTTGTAACCACAAG	161436
rs554986645	snp	A/C	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88745890	CGTGTATACCTATGT[A/C]ACAAACCTGCACGTT	161436
rs554988619	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646749	TGGATAAGTTTTAGT[A/G]AAGCAGTTACTTATA	161436
rs554991171	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88758858	AATACATGCTACAAC[A/G]TGGATGAACCTTGAA	161436
rs555007925	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88700974	TTTTTTTGCCCTACT[C/T]TTACAGATGCTGTAA	161436
rs555020188	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783921	TTGGGTCATAAGACA[A/G]GTCTTAAAATGTTGA	161436
rs555021762	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750864	ATGTATCTACCTCTT[A/G]CTATCAGAATACTGT	161436
rs555032674	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691110	GGGTATCTGGCAGTG[A/G]AATCTCAGTCTAGTA	161436
rs555059450	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749919	TACTGTGAAAAGTAC[G/T]GGTTTAGAGCAGGGG	161436
rs555112570	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678053	ACTCAAATGCCCATC[A/G]ATATTAGACTGGATA	161436
rs555113649	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776875	GACAGAGCAAGACCC[C/T]GTCTCAAAAATGAAA	161436
rs555117082	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742268	TTACACACACACACA[C/T]GCTTTCCAATACAGT	161436
rs555142469	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700473	CCCTGAGTTATTTTC[A/G]GGAAACAAAGCATCA	161436
rs555144613	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708783	TTAAATGTAAATTGG[A/G]TTATATGCTCACAAG	161436
rs555194874	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653638	GCTTTGCATCCCAGG[A/G]ATGAAGCCGACTTGA	161436
rs555212932	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640458	GAATGACTTTTGGGT[A/G]AACAATGAAATTAAG	161436
rs555213644	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635563	AGATAAAACTTATCA[A/T]ATAAAATATATTCTA	161436
rs555224952	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677273	AATTGAAGCTGGACC[C/G]CTTCCTTACACCTTA	161436
rs555228453	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731376	TTCCAGTCTCATCCA[C/T]GTCCCTACAAAGGAC	161436
rs555237927	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88774044	TAATCGCTCGAACCC[A/G]GAGGCAAAGGTTGCA	161436
rs555275539	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731053	TTTTTGTAGTTATAA[C/T]AGCTGCTTTAATGTC	161436
rs555276417	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623655	CTGACCTCGTGATCC[A/G]CCCACCTCGGCCTCC	161436
rs555278655	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88644629	CAAAGATGACCCATT[A/C]TGTGGTCCACTAGAC	161436
rs555308574	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88740866	TGAAAAGAAATCTAC[A/G]TAAAACTTAGATTAA	161436
rs555378573	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733861	TACTGGAAGAATATA[C/T]TGAAAATTTTTAAAA	161436
rs555386396	in-del	-/ATATATTTTTTGTATTTTTAGTAG			intron-variant	EML5	GRCh38.p7	14:88639742	CCATCATGCCCAGCT[-/ATATATTTTTTGTATTTTTAGTAG]ATACGGGGTTTTGCT	161436
rs555389234	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679560	AGCCAGCCGTGGTGG[C/T]GCACGCCTGTAGTCC	161436
rs555406537	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698112	GTTATTCAGCCAAAC[A/G]TTACCAGTAACTTTT	161436
rs555425545	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88641587	CATATGATTATCTCA[A/T]CAGATATGGAAAATG	161436
rs555529940	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624086	TTTTTGTTTTTGTTT[C/T]TGTTTTTTAAATGGG	161436
rs555542698	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705264	TATGACAAAATCCTA[C/T]AGGCAAATAGAAGGC	161436
rs555546228	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632266	TCCACATTCACTCCT[G/T]CCACCCTGCTTAACT	161436
rs555559441	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615029	TGTTGCTCCCTAAAA[C/T]CCTTACATTGTACAC	161436
rs555562397	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88683130	CTTCTATATGGTTTT[A/T]AATATCTTTCCAGAA	161436
rs555590845	snp	C/T	1.65685e-05	0.00287819	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740504	TAGGCACAGTATTGT[C/T]TGAAGGTCACCCGTC	161436
rs555594304	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777135	AAAGACTACTTCAAG[A/G]CATTTAATAGTCGAA	161436
rs555599844	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88770773	ACTCAACATTTATGG[A/T]TTAATTTGGGAGACA	161436
rs555600054	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721588	ACTGAAACTGGACCC[C/T]TTCCTTACACCTTAT	161436
rs555607815	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88735529	TTTCACCTTTTGGGA[C/T]TATAATTAGTTCTGT	161436
rs555609354	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689827	TTATGAACAGAACAG[A/G]CAAGACAACAAAATT	161436
rs555617956	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684953	GTCAACTTTTGGCTC[G/T]TATATATTGAAATAA	161436
rs555637064	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729331	TATGATATTTGCTGG[C/T]GACATTCTATGCTCT	161436
rs555644458	in-del	-/CCCTGA			intron-variant	EML5	GRCh38.p7	14:88710073	TCACCTCTCCATTCT[-/CCCTGA]CCCTGACCTGCTCAC	161436
rs555670256	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614433	ATGTAATTTAGTCAT[G/T]TCTATTTTTAGTATT	161436
rs555673295	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789035	ACCATTGCACTATAG[A/C]CTGTGTGACGCAGAG	161436
rs555675432	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88728440	TATCAATAACACAAA[C/G]AGTTGTTTAACATAC	161436
rs555700346	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88772388	CTCATCATTTACCTC[A/G]GTAAAAACCCAATAG	161436
rs555704361	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683830	GTAAGGAGCATCTAC[A/G]AAAAACCCACAGTTA	161436
rs555726843	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630504	TACTCCTTCCTAGAG[C/T]GTAAGTGATTCAGGG	161436
rs555738199	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724206	CTTGAACCTGGGAGG[C/T]GGAGGCTGCAGTGAG	161436
rs555761074	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779302	TGAGTATCATATCAG[A/G]AGTTTAAATATAGCA	161436
rs555769377	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88675506	CCTAGGCTGCACAGA[A/G]TAGAGGGGCCCGTGG	161436
rs555769953	in-del	-/AACAA	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88664889	TGATACTTTGTATTT[-/AACAA]AACTCCCTCTAAATT	161436
rs555780931	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692103	GGATGGGCTGGGCAC[A/G]GTGGCTCATGTCTGT	161436
rs555799691	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787370	AAATATTTCTTGGAT[C/G]AGAAAACTTTGAAAT	161436
rs555817612	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88660199	GAGGTGGGAGGATAA[C/G]TTGGGTCTGGAAGGT	161436
rs555845220	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88769011	AGCAATATCATCTCC[A/G]AAGGGGCAAAAATTA	161436
rs555880094	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88715824	CACACCACCATACCC[A/G]GCTAATCTTTTTGAC	161436
rs555895353	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755053	CAAGTGATCCGCCTG[C/T]CTCAGCTTCCAAAAG	161436
rs555898640	in-del	-/A	0.00438332	0.0466095	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613658	ACAAAAAGGGACCAC[-/A]AAAAAAGGAAGGAAA	161436
rs555907094	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713285	TAATCTCAGCTACTC[A/G]GGAGGCTGAGGTAGG	161436
rs555921145	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730924	TTATTCTTTAGCACG[C/T]ACTTAGTGAAGAAAA	161436
rs555923166	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777085	AGTATCCAAGTACAA[A/G]AAGGATATAGAACAC	161436
rs555979898	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704831	GAACCAAAATTCAAA[A/C]AAATAAATGAAAGAT	161436
rs555991349	snp	A/C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791859	CGCCACCCTGGGCGC[A/C/G]CTCCCCGGGAGCAGC	161436
rs556039318	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763823	TTTTTCCTGCTTTTA[C/T]AAGGAAAACATTCAG	161436
rs556039738	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625630	TGGTCTTGAACTCCT[A/G]ACTTCAGGTGATCTT	161436
rs556058884	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88686678	TTGCTGAGTATGGTG[A/G]CAGGCGCCTTTAGTC	161436
rs556090325	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668446	TCAGAAAAAAAAAAG[A/G]GAATGATAAATTGTG	161436
rs556104365	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88676447	TCACGAGAACAGCAC[A/G]GGAAAGACCTGCCCC	161436
rs556126010	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794385	AGATGTCATGAAAAG[C/T]AAACTCTGAAAGAGT	161436
rs556138092	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88763122	ACAAAAGCAAACAAA[G/T]TCAAAAGCTAGCAGA	161436
rs556161389	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775780	AGGCAGTAACCAGGG[A/G]CTGATTACAGCAAGC	161436
rs556232683	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737047	AGAGCTGTTTTGTCA[C/G]TCAGTAAAACTCTTT	161436
rs556248470	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670075	AATCCCAGCACTTTT[A/G]GGAGGCCGAGGCAGG	161436
rs556303032	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706124	GAACTAATATTTTAA[C/G]TTGAAATTTCTACTA	161436
rs556307863	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693444	TCAGATCTCATGAGA[C/T]GTATTCACTTCCACA	161436
rs556308145	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687038	TGTATCATAGAAAAT[A/G]GACTTTTGAAAAGAT	161436
rs556319310	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655405	TTAATAAATGGTGTT[A/G]GGGAAACTAGCTACC	161436
rs556346497	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700154	TTCCAAATTATAGTA[C/T]AATTAGTCATGTTAT	161436
rs556356295	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88732369	TTGTCAAAGATCAGA[C/T]GGTTGTAGATGTGTG	161436
rs556357908	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657955	ATTTACCTTAACAGT[A/C]CTTATTTAAAATTCA	161436
rs556436962	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685935	GGAACCCACAGATAC[A/G]GAGGGCCAACTATAT	161436
rs556476599	snp	A/C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761735	GATTCTTGGGTCAAA[A/C/T]GGTATTTCTGGTCCT	161436
rs556483161	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699529	ACAGGCTATTAACAC[C/T]AATAAATATGAAAGA	161436
rs556492197	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88790793	AAAGACAAGACACTG[C/G]GGTAAACTCTACTCT	161436
rs556493856	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88665695	GGAAGGGGCAAGGGG[C/T]AAAGGAGAAGGGGCG	161436
rs556501748	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665032	GTAAAATGAGTGCAA[C/T]TTCAAAAGCATTAAG	161436
rs556526917	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736249	TGTGATCTGCCCGCC[G/T]TGGCCTCCCAAAGTG	161436
rs556552259	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663686	TCTTCATTAACATTT[A/C]TTTTTAAAAATGTAT	161436
rs556585490	in-del	-/A	0.00478085	0.0486577	intron-variant	EML5	GRCh38.p7	14:88686140	GGGAAATCATCCTAG[-/A]AAAAAATCAGGTTTG	161436
rs556614576	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88761255	TGTGCAGAACGTGCA[A/G]GTTTGTTGCATAGGT	161436
rs556647362	in-del	-/AAGA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88776522	GAATTGATCAAGCAG[-/AAGA]AAGAATTAGTGAGTC	161436
rs556654851	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722291	AGAAATATAAATCAT[C/T]CTATTACAAAGATGC	161436
rs556669594	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703882	ACATTTTACTTAATT[G/T]TTTAAAGAGGCCCAT	161436
rs556689249	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760920	AGCTTTTGTAGACAG[C/T]ATTGCTGTAAAATTT	161436
rs556691109	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88791408	TGTAAAGGACAAAAA[A/G]TGCTGTGCTTGAGGC	161436
rs556706515	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711290	GACCTGGTGGGAGGT[A/G]ATCGAATCATGGGGG	161436
rs556726860	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88757842	CCTTTCTCTCTCTTT[C/T]TCTCCTTTCTTTCTA	161436
rs556756285	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88701172	GTGATTTTGCCTTCC[A/G]AGGGACATCTGGGTA	161436
rs556763787	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765439	CATGATGTTACCACC[C/T]CCATCTTCCAATCAG	161436
rs556781373	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88642755	TAGAAAGTTCTGAAA[C/T]ATGAAATATTTTTAT	161436
rs556793031	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88774035	GAGGCAAGATAATCG[A/C]TCGAACCCGGAGGCA	161436
rs556836756	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745073	ATAAATTCCAAATAG[A/T]CATGTGCAAAATGCT	161436
rs556842907	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641839	ATTAATTACAAATCA[A/G]AAAAGTAAAAATAAA	161436
rs556842971	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88668347	AAGAGATAGCACTAG[C/G]AAAGGAAACAGAAAA	161436
rs556850028	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88721458	AGAATTCAGAAATAA[G/T]ACCACACATCTACAA	161436
rs556851726	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787506	AAAATAATAAAGGAA[A/T]ATAATTAAATGTAAA	161436
rs556873430	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88671479	AAATCAATGATACTA[C/T]GAAGCAACTACATTA	161436
rs556879723	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630721	CTCAGTCAGGCTAAA[C/T]GGAAGGATTTTTAGG	161436
rs556912186	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88634648	TCATTTCAATCATAC[A/G]TACTTATTAACATGC	161436
rs556952672	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88776381	GATAACACAGAGAAG[C/G]AAATCACAATTCTGT	161436
rs556979651	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710687	ACAATCTCAAGCTGA[C/T]TCACAAGTGCCTAGA	161436
rs556983503	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651082	TATGAACCTCTTCAT[A/T]TGTAATCTCCTTTGA	161436
rs556995707	snp	A/G	0.000480551	0.0154934	intron-variant	EML5	GRCh38.p7	14:88681867	GAGAGCTTAATCTAC[A/G]TTCAAGTGTGAGAGC	161436
rs556997205	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643874	AGCAATCACCATCGC[A/C]CAGCTTTACGCCTTG	161436
rs557016689	in-del	-/T	0.379365	0.213927	intron-variant	EML5	GRCh38.p7	14:88769969	CATTATGTGCAGTTT[-/T]TTTTTTTTTTTTGGT	161436
rs557024681	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675286	TGCAGCAAACTTCTG[C/T]CTGGGCATCCAGGCA	161436
rs557041031	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764854	TTTATTTTGATTCCA[C/T]TATGGTCAGAGAACA	161436
rs557047220	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622111	TTTAGTTTCTGCACA[G/T]GAGTGAGAACATGTA	161436
rs557052073	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718806	CTTAAGATGGGACAC[A/G]TTGAGCATGTTCTAA	161436
rs557053153	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745972	CTTATGCCAATGCTA[C/T]ACATATCAAATCATG	161436
rs557095763	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88713478	ACTTGTTAATTTATT[A/T]ACTTATTTGTTTAGT	161436
rs557120329	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613435	GTTTCACTATAAATT[A/G]TAGAACAAATGGGAA	161436
rs557121723	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88740320	ATACTATATTACGCA[A/G]TCTATCATTCTAAGA	161436
rs557136897	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651270	CAAAATATTTAGCAG[C/G]GTTGAAATTGTAAAG	161436
rs557168277	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645993	AATTTAGTTTATTAT[C/T]TTTATCTCAACCATT	161436
rs557194592	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658762	GGTATTTACTTATAG[C/T]AGTGAAAAAAATTAA	161436
rs557218685	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701771	TAACTGATTGATCTT[A/T]AGCAAATTATTTAAT	161436
rs557234076	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88689277	AAAAGGCATATCATA[C/T]AGATCAGAGAGGTAT	161436
rs557236917	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88741078	TGAGGCACAAGAATC[A/G]CTTGATATCAAGAGG	161436
rs557239944	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758609	GCCTCTTTGGAAAAC[C/T]GCTTGGTAGCTATTC	161436
rs557255171	in-del	-/A	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88791025	AAAACAAAAACAAAC[-/A]AAAAAAACCAACTGA	161436
rs557266614	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704629	TTGTCCCAACAATGT[C/G]CTTTATAATCATCTT	161436
rs557278719	snp	A/C			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615473	ATGAAAATTATCCAA[A/C]TTGGGTTTTTGAGTT	161436
rs557282365	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628555	CCTATAAAAATGGAT[A/G]GGTCAATTCAGCAGT	161436
rs557298896	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784959	GAGTCTATCAACAGA[G/T]GAATGGATAAAGAAA	161436
rs557363368	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688517	CCACTTTCAAAATGT[A/G]CTCAATTATAAAGAA	161436
rs557370244	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88738685	GAATCTTTCTCCTAA[C/G]AATGAACCTAAACTC	161436
rs557404758	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785779	CTGACTGGATTACTG[C/T]AACAGTCTCCTAAGT	161436
rs557421118	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630109	GATCTCGGCTCACTG[C/T]AACCTCTGCCTCTGG	161436
rs557436888	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742352	AATGAATTTTAAGTT[G/T]CATTTAACTAATTTG	161436
rs557437664	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781484	TACTACCACTAATTA[C/T]AATTACTAAAAATAG	161436
rs557439127	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751736	CCTGAAGAACACTGA[C/T]ATTTAAGAAGCAGAC	161436
rs557440862	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780980	AATGTTTGATTAAAT[C/T]ATCTGGTACTATATA	161436
rs557452224	snp	A/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88650498	AACAAAAACATTTAT[A/T]AAAAAAGAAAAAGGT	161436
rs557492164	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767869	TATCATTACCTAAAC[A/T]AAAAACCTTATTCAA	161436
rs557492238	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775070	CAGCATTCACCACCT[A/G]CTAACTGAATAGCCC	161436
rs557499101	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88735619	TGCCTCTATGTAAGG[C/T]CTTATCTATCAAAAT	161436
rs557532073	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88620399	AGAAGATATGTTTGA[A/C]ATCACAACTTTAGTT	161436
rs557532251	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774178	ACAACTGATTACTGG[A/G]CTCTACACTTAGAGT	161436
rs557573283	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88743398	CTATCATTATTTGTC[-/A]AAAAAAAAAATTTAA	161436
rs557583359	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718025	CAAAATCAACAGGAT[A/G]TGGTGCTGATGGATT	161436
rs557584036	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88646863	GGTAAAGAACACTAA[A/G]TAACAGTATCCCATT	161436
rs557589214	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783703	GAGAGACAGGCCCCA[A/G]TATAATAGCTGGAGA	161436
rs557594027	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633276	CATCAAGGTATTTTA[G/T]TTTTTATTTATTTAT	161436
rs557596922	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88720943	TCTCGGGATATAAAA[C/T]CAATGTGTAAAAGTC	161436
rs557611281	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88673396	ATACCTCAAAATAAT[A/G]ATGATAAACCCACAG	161436
rs557624576	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774413	GTTATACATTGGAAC[A/G]AATCTTGAAAGAGGC	161436
rs557663794	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88679509	CCAGCCTGGCCAACA[C/T]GGTGAAACTCCATCT	161436
rs557664208	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723007	AAGACATATTTGAAG[A/G]AGGAGGGAAGGACAG	161436
rs557696475	snp	A/C			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767770	ACAGTTTTCTTGTAT[A/C]CCTCATCACACTTCA	161436
rs557707205	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790544	TCTAGTTTCAGAAGA[C/T]CTTAGTGCTATACTG	161436
rs557771953	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705859	AATGTCTGTGCAAAT[A/G]TAAGTGAATATAACC	161436
rs557797810	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691781	CTTATTTCCCAAGTG[A/G]TTAATGAACTCTGTG	161436
rs557807337	snp	C/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88678313	GAGGGAGAGCATTGG[C/G]ATAAATAGCTAATTC	161436
rs557813316	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88657001	TTGTTTTTGTGGGTA[-/T]TTTTTTTTTGAGACA	161436
rs557823553	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88633904	GTGTGAGCTACCATG[C/G]TTGTCCAAAAAAAAC	161436
rs557828791	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779902	CAAAATTTTTACTTC[C/T]ATGTTACTGTGAGGA	161436
rs557847393	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88679129	TGGCCTTCTTATAAG[A/G]ACATCAGTCACTGGA	161436
rs557849770	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88655315	ACAGAGGCCTCAGGA[A/G]TAATGCCACATATCT	161436
rs557867014	snp	A/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88623037	TTTTTTTTTTTTAAG[A/T]TGTAGTCTCGCTCTG	161436
rs557870451	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88647021	TGAAAACACTAGTGA[A/G]ATACCTCCTGTAATA	161436
rs557884080	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687300	CCCAAAGAGCTACTA[C/T]ACCATCTTTTCCTCC	161436
rs557899242	in-del	-/TTTCAA	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88724452	TAATCAGAATAACCC[-/TTTCAA]TACTATTAGCAATGT	161436
rs557899290	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671259	GGGCCAATATTCAAC[A/G]TTCTTAAAGAATTTC	161436
rs557930434	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88617435	TACAGGCTGAGCCAC[C/T]GCGCCTGACTGAAAA	161436
rs557940076	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782213	AAGATCAATCTTACT[A/G]TGCAAAGAGACTGGC	161436
rs557944545	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88624874	GAAGGTCGGAGAGGA[C/G]ACTCTGTGTAGCCTA	161436
rs557951996	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88714262	TACAGTGGTACTTTA[A/C]CATACACTATACTCA	161436
rs557954085	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713954	ATGACCCTCCCATCC[C/T]GACCTCCCGAATAGC	161436
rs557981619	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714649	TATCAAAACATTACA[C/T]TGTAAATTTTCAATA	161436
rs557987210	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729769	TTTTGCCATGTTGGC[C/T]AGGCTGGTCTTGAAC	161436
rs557990844	snp	A/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88713382	GGGCAACAGAGCGAA[A/T]CTCCGTCTCAAAAAA	161436
rs558000211	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722345	CACTATTCACAATAA[C/T]AAAGACATGGAATCC	161436
rs558013724	in-del	-/TAAT	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88659529	AATGATGACTCTTAA[-/TAAT]TAAGTCAGGGTGAGG	161436
rs558053036	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698307	GTTTCACTCCTGTTG[C/T]CCTGCTGAAGTGAAA	161436
rs558068431	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88735620	GCCTCTATGTAAGGC[C/G]TTATCTATCAAAATT	161436
rs558088347	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766224	TGAAAAAAGAACAGG[A/G]TAACAGCGATGTTCA	161436
rs558091523	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705303	TTAATATACCAAGCA[A/T]TTAATATAAAAAAAA	161436
rs558095535	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654353	TCTTGCTTCTCTAGT[A/T]CTTTTAATTGTGATG	161436
rs558098514	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676957	TCTCCCAGACTGACG[A/T]GCAGTGGCACAATCT	161436
rs558099041	in-del	-/ATAACT	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88771023	ATCTCTAAATTTATC[-/ATAACT]ATAAGGAAATAACAT	161436
rs558120853	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88623466	CGCTCTGTCACCTGG[C/T]CTGGAGTGCAGTGGT	161436
rs558146516	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716637	TATTTTGGTATTTTT[G/T]ATAGCATTTTTGTTT	161436
rs558151152	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760091	CCTTTGTCCTACATG[A/G]GACTTGCAAATATTT	161436
rs558173084	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720252	GAAATAGCCCAACAA[C/T]TGATAAGGAGGGACT	161436
rs558185948	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766655	TCCATTTGCCTTCTG[A/G]TATTTTATTACCTTG	161436
rs558207571	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681376	ACCACTTTGGCAGGC[C/G/T]GAGGTGGGCAGATCA	161436
rs558210976	snp	G/T	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684241	GAAGTTAAAAACTCG[G/T]CTCACTGCAAGCTCC	161436
rs558231154	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780194	TGACCTCTAAGTGAT[A/C]CACCTGCCTCAGCCT	161436
rs558232707	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88673189	AAAGATTATCCACCA[C/T]GATCAAGCTGTCTTC	161436
rs558258227	snp	A/C	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88630554	ACTAATAAGTCTGAG[A/C]CCACTGTGATAATAC	161436
rs558270949	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680828	ATGGGATTCCCACAG[A/G]TAAAGTCCAATCAAA	161436
rs558282211	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641143	CCTATCAAAAAGCCC[C/T]GGACCAGATGGATTC	161436
rs558283806	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88725236	GCTAGAGGGTGGTGA[A/T]GGTTGCACAACAATG	161436
rs558318823	snp	C/T	0.000189879	0.00974185	intron-variant	EML5	GRCh38.p7	14:88705873	TATAAGTGAATATAA[C/T]CTATAATTAACATGA	161436
rs558324659	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731315	ATGAGTGAGAACATG[C/T]AGTGTTTGGTTTTTG	161436
rs558363675	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776697	ACCAACGTGCGTAAC[A/G]TGGCAAAACCCTGTC	161436
rs558399963	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784695	CACCCCAGTTAAAAT[A/G]ACTTATATCCAAAAG	161436
rs558418305	in-del	-/A	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88625784	CACAAACATTTCAAT[-/A]AGTCTTTTTCTCAAA	161436
rs558418867	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662744	GAGATGGGGTTTCAG[C/T]ATGTTATCCAGTCTG	161436
rs558420382	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88660097	CATAGGCAACATCTG[A/G]AGACCCCATCTCTAC	161436
rs558449455	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615710	CTGGGCATTTCTCCC[C/T]GTTACAGTCTTGGGT	161436
rs558482144	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662064	TATATATCCACTGTG[C/T]GTTCTAGATGCTAAG	161436
rs558549830	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770393	TAAATTTTATATATG[A/G]TGAGGTATATGCTGG	161436
rs558551972	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665769	AATAAATAGACAGGC[A/G]TGGTGGCACACACCT	161436
rs558575420	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666386	CATGTGCCACCAGGC[C/T]TGGCTACTTTTGTAT	161436
rs558620455	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664704	CTAGAGTTAATTTTC[A/C]TTTTCTTTATGGAGA	161436
rs558645135	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768659	TCAGGTGACCCACCC[A/G]CCTGGGCCTCCCAAA	161436
rs558651696	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775890	GTCATTCACCCCCAG[C/G]TTTAGGTGGCTCAGA	161436
rs558659003	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626558	GGAGATGGAGGCTAC[A/G]GTGAGCTATAATCGC	161436
rs558682519	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88695175	AAGTGGGTTCACAAG[A/G]GATAAATCTACAAAG	161436
rs558701090	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687893	CTACCCTGGGCAACA[C/T]AATCTCTACCAAAAA	161436
rs558718864	snp	A/C	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88702024	TTCTACTTTGGTAAA[A/C]CTGAATAGATTACTA	161436
rs558729306	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666103	AAATTAAGTTGATGA[A/G]AAAGAATGAGAGATT	161436
rs558733768	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792536	CCGCTCCCGCTCGGG[A/C]CCGCGGCGGCGACGG	161436
rs558741903	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707023	TCCAGATATTTAAAA[A/C]AAATCTTTCAATTTG	161436
rs558788563	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671910	CATAAAACAAGTTCT[C/T]AGAGACCTACGAAGA	161436
rs558812255	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88659464	TGATCCACCTGCCTC[G/T]GCCTCCCAAAGTGCT	161436
rs558866550	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791852	TTCAGGACGCCACCC[C/T]GGGCGCGCTCCCCGG	161436
rs558879679	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88658885	AAATAGATACAATAA[C/T]TGAGAAAGGATACAC	161436
rs558883158	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682728	TCTTGTTGAGCTCAG[C/G]TGACAGGTGGGAGAT	161436
rs558903883	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787048	AAAAGGAACTGAAGA[C/T]AGTATAAGCAAATTC	161436
rs558925361	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643642	AAGAAAATTTTATGT[C/T]CATTGTTAATCAAAG	161436
rs558946630	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88791388	GCTTTTAATATATTT[G/T]CCTCTGTAAAGGACA	161436
rs558955676	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753827	TTTTAATAGACAACC[C/T]TTAAGGTAACTGAAA	161436
rs558982163	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88784185	AGTTGTAAGTGCCTA[C/T]ATCAAAAAAAAGGAA	161436
rs559026384	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88652474	GTGCAAACTCAAATC[C/G]CTCTGACGAAGCTTT	161436
rs559053809	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715600	TGTAAGGAGCTAAAT[A/G]TGCAAAATTACATTT	161436
rs559096854	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676532	TGAGATCTGAGTGGG[A/G]ACACAGCCAAACTAT	161436
rs559097328	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88621730	TTATAAATACACTTA[A/T]TAAGTACAAACACGC	161436
rs559097382	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88728670	CAGGGGTGGCAGAGG[C/T]GGAAGAAAATCCACC	161436
rs559098242	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730970	GTTTTTTTTAACCAA[C/T]AGCATTAATGGTGAA	161436
rs559113314	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711877	TGGAACCCAAGAGGT[A/G]GAGGCTGCAGTGAGC	161436
rs559117985	in-del	-/A	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88685353	TCTTATAAGTCTATG[-/A]TTCTATTCTCACATT	161436
rs559162603	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88636487	CCAACATGGTGAAAC[A/C]CCGTCTCTACTAAAA	161436
rs559173217	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635520	AGCTTGAATGTCATC[A/G]GCCTAAATATTTTAA	161436
rs559175495	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645182	AAGCGTGCACCACCA[C/G]ACTCAGCTAATGTGT	161436
rs559183545	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88751347	AGAGACAGTTTGTAG[A/G]AAAGTAATAGTACAT	161436
rs559184561	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88665003	TAGATAATGAATACA[C/T]GGAAATTAATGGAGT	161436
rs559187798	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673304	ATGATTATCTCAGTA[C/T]ATGCAGAAAAGGCCT	161436
rs559208068	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747805	AGTGGACAGTGAGAC[C/T]GAAAGTATGAGAGAG	161436
rs559217262	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649626	GTTAGGTTTGTTTTT[A/G]CGAGCCTCTGAAACT	161436
rs559223249	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737740	TGTACCTAGTTCCTA[C/G]CCATCCTTCAAGACA	161436
rs559233408	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634730	TTTAATGAGTTACAT[A/C]AACTTTTAATTATAA	161436
rs559235431	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88731527	AGTGCCACAATAAAC[A/G]TACGTGTGCATGTGT	161436
rs559237585	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88696148	TTCTAGTTTCTTAAC[G/T]GTTAGCAACTCTTTG	161436
rs559261804	snp	G/T	0.00835141	0.0640778	intron-variant	EML5	GRCh38.p7	14:88737165	ACAGAGCTGTAACCA[G/T]GCAGCACTCCCCTCC	161436
rs559264117	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745768	CAATAAAACTGTTTT[A/T]AAAAATGTAAAGAAA	161436
rs559264752	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614639	AATAGCAGTCTACAT[A/G]ATTTTCAATCTTCAG	161436
rs559266479	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690110	CCCGATACAACAACA[C/T]GACTGAAATCACTAA	161436
rs559269773	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88683419	ATGCTACCAATTAAA[C/G]GAGTTTAACAGTTGG	161436
rs559293205	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768560	GAATTACAGGTGCCC[A/G]CCTCCACACCTGGCT	161436
rs559303443	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697032	GAAATAAAACAAGAG[A/C]TTTTTACAGCTTGAC	161436
rs559329217	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645560	TTTCTATGAACGTTC[C/T]ACACTGTTAGCAACA	161436
rs559351225	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727082	GGTATCCTTTTAGCA[C/T]AGTTATAGTGTCACT	161436
rs559380252	snp	A/G	5.71303e-05	0.00534433	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626794	CTAAGGCAAGAGAAT[A/G]TAAAGTAGTCAAAGT	161436
rs559386449	snp	A/G	0.0460142	0.144533	intron-variant	EML5	GRCh38.p7	14:88731755	GACTTTTTAATGATC[A/G]CCATTCTAACTGGTG	161436
rs559396918	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88641812	TCTAGACACCCCACC[A/G]CTAGAAAAGTGATTA	161436
rs559412478	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644339	AGTACTCAAATACAC[C/T]GATTTTCATGAAAAC	161436
rs559424715	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88738805	AAACTTACATTTATA[C/G]TCACTGAAAGAAAGA	161436
rs559431434	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778837	GGGATCAATAATGCA[A/G]TTTATCAAAGATATT	161436
rs559445711	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88726050	GAATTTATCTATCTA[C/T]AATTCAACACAAAAT	161436
rs559462089	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673550	GACAAGAGAAAGAAA[G/T]AAAGTGTATTCCAAT	161436
rs559463415	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772836	CTACACTCCAGCTAC[A/C]CTGGCCTTTCTATCC	161436
rs559470588	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88620502	AACTTAATGGACATG[A/G]CTAAGTGTTAACATG	161436
rs559473177	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88708791	AAATTGGATTATATG[C/T]TCACAAGGTACCTTT	161436
rs559486172	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88659866	ATTAATATGAGCAGT[C/T]ACTCAAGATCACCAG	161436
rs559487904	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720177	AAAAGGCTCATGACC[A/T]GATGAATTTATAGCT	161436
rs559491033	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776989	GCCTTAAAGAGGAGC[G/T]AGATAAAGAGACAGG	161436
rs559495209	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88707525	ATACAATGATGCTTA[C/G]CTTCCTTTTGATATT	161436
rs559512737	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88746987	AGTCTTCAGGGTTGG[C/G]TGTGTCTTCAAGCAA	161436
rs559515105	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725662	AAGAAGAAAGCACAC[A/G]ATGTGTTTTAAAAGG	161436
rs559540744	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677367	AGAAGAAAATCTAGG[C/T]AATACCATTCAGGAC	161436
rs559546488	in-del	-/AAAA	0.428937	0.17459	intron-variant	EML5	GRCh38.p7	14:88759685	AAGTCACCATCTCTT[-/AAAA]AAAAAAAAAAAAAAA	161436
rs559551493	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711762	ACAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	161436
rs559552107	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765746	AGAAATTGAGTCCCC[C/T]GGAGAATTATTTATA	161436
rs559555468	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651751	GTATTTATCTAATAA[A/T]TACATATGTAGCGCT	161436
rs559562406	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88655422	GGAAACTAGCTACCC[A/G]TATGTAGAAAACTGA	161436
rs559617590	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764907	TTTAAATTTGTTAAG[A/G]TTTGTTTTATAATAT	161436
rs559618330	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638617	TTGTCAAGACCAACT[C/T]AGATAACCAGAGTGA	161436
rs559645005	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88697989	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	161436
rs559646697	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764159	TTATTAGCTTATTTT[A/G]TTGAGAATTTTTACA	161436
rs559651820	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756876	TGGGCTTAGAGGAAT[A/G]TAATATTTGTAAGAT	161436
rs559683027	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767410	CAATTTTCCCCATAA[C/T]TTCCAGCTCCCAGAG	161436
rs559686553	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733318	TTCAGGGCAAAAAGC[A/G]GCTTTGGCACAATGC	161436
rs559716486	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88754151	AAAATAAAATTAAAA[C/T]AAAACATATACAGCT	161436
rs559722410	snp	A/G	1.66571e-05	0.00288587	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616106	CTCTTAACTAGTAAC[A/G]TAGTCTGCTCTTCAT	161436
rs559744385	snp	C/G	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88619489	GGATTACAGGTGTGA[C/G]CCACAACACCCAGTC	161436
rs559757113	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88774452	TGTACCAATAATGAC[A/T]TGACTCATTTTCTCA	161436
rs559760294	snp	A/G	0.0130921	0.0798413	intron-variant	EML5	GRCh38.p7	14:88624210	GCCTCCTGAGTAGCA[A/G]GGACTACAGGCATGT	161436
rs559799163	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731176	CTGCACTCATTAACT[C/T]GTCATTTACATTAGG	161436
rs559816851	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735710	CAAAATGACAAATGT[A/G]TAATGATATTCACTG	161436
rs559826831	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88728834	GAAGTAATCTCCCCC[A/C]AAAATAGCAAGGAAT	161436
rs559873196	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88681742	CAATTACGTTTCTCT[A/G]TGTGGCACCATGAGC	161436
rs559908131	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613534	GCTATTTAATAGCCA[C/T]TGCCCAGACACATAT	161436
rs559911826	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688631	TCAATCAGTGATGTG[G/T]GTAACACCTTGCATA	161436
rs559948231	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88632483	CTACAGCATCCTGCA[A/T]GAGATGACCACTATC	161436
rs559949944	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88787990	TTCCTGGGCTCCAAC[C/G]CTAGAAGATTCTGAC	161436
rs559953107	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88718174	AGGGATATCATGAGT[G/T]CAGTTTTGGAAATGC	161436
rs559962828	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88703257	AGTAAAAGGTATAGA[A/G]AAGTATATTTGTATT	161436
rs559974662	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669551	CCTGCAGGAATTTCA[A/G]CAACTCCAGCCAGAG	161436
rs560001744	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710838	CTAATTTTCTTAGGC[G/T]TTGGTAAAATATTCA	161436
rs560010228	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655591	CATGACTAAAACACT[A/G]ACAGCAATTGCAACA	161436
rs560033167	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773626	AAAATTAAAAACAGA[A/C]ACAAACAACAAACGA	161436
rs560039265	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88789875	AGTAATATTTGACCA[A/T]TAAGTTTTACATAAG	161436
rs560042081	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767976	GTTATTCCTCCTTAG[C/G]AACTTCCAGTCTCTA	161436
rs560044514	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710155	CTTTCAGAGAGATTA[C/T]GGTCAAGAGCAGGTG	161436
rs560067861	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670262	GAAGTGGAGGTTGCA[A/G]TGGGCCAAGATCATG	161436
rs560085480	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714251	TTTGACTAAGATACA[A/G]TGGTACTTTACCATA	161436
rs560093906	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774186	TTACTGGGCTCTACA[C/G]TTAGAGTTTCTAATT	161436
rs560094772	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705372	CTAATATAGTCATAC[A/G]TTGCTTGAGAAATTA	161436
rs560097587	in-del	-/AACTA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88637426	ACCATGACATTTCTT[-/AACTA]AGAAAGAAAACCACA	161436
rs560114218	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785143	AAAAATCAAAACAAC[C/T]GAACTAATGGACATA	161436
rs560122249	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88721853	GAGTGGGAAAAAATA[C/T]TTGCAATCTATCCAT	161436
rs560133468	snp	C/T	5.4074e-05	0.00519943	intron-variant	EML5	GRCh38.p7	14:88704992	ACCTTTAAAAATGTA[C/T]ACAAGTAGAAATATT	161436
rs560142764	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714823	ACAATGCCTGAAATA[C/T]TAGCTCAGATCTTCT	161436
rs560209404	in-del	-/A	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88672621	AGGGGCCGGTTTTTG[-/A]AAAAAAATTAATAAA	161436
rs560236921	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781647	ACTGAATCATGGTGA[C/G/T]GATTACTCTCATGCT	161436
rs560246440	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752958	CTCAATAAAATCCTC[A/C]ATATACACCACCCTT	161436
rs560274402	snp	A/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88678447	GAACTTAAAATAACA[A/T]AAAATAAAAAAAAAT	161436
rs560335405	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88677473	TAATTAAACTGAAGA[A/G]CTTCCTCACAGCAAA	161436
rs560357834	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88754693	AATAAGGAAATAAAT[A/G]AGTAGTATTATTAAA	161436
rs560361265	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693922	ACCACAGGTACACAC[A/C]ACCATGCCCAGCTAA	161436
rs560370222	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699815	AGTTAATACACTGCT[A/G]TGTTCTAAGAAGGAA	161436
rs560405041	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707276	AGGGATATATTTTAT[G/T]TATTTATTTATTTAT	161436
rs560406964	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699166	AAGTCTTAAAAGGAG[C/G]AGAAATTAGATAAAG	161436
rs560443655	snp	A/G	7.05579e-05	0.00593919	intron-variant	EML5	GRCh38.p7	14:88706232	TTATTTGACAGGGAA[A/G]CTGTTTAGCTAATGC	161436
rs560474579	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88780721	CCTGGGATTACAGGC[A/G]CGCGCCATCATGCCC	161436
rs560478252	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760433	TCTTTTCTCCATTGA[C/T]TTCCCCAAGCACTTT	161436
rs560504160	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653769	TTTCTTTTTTTGTTG[G/T]GTCTCTGCCAGGTTT	161436
rs560527442	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702068	ATAAAGAGACATAGT[C/T]CTTTGGTTTGTCACA	161436
rs560557802	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88710225	TGAAGAGGGGTGGAA[A/T]GCTTTGGGCTGAAAT	161436
rs560571899	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701232	CTCAGGGAAGTGGGT[C/G]TTCCTGGCTTCTAAT	161436
rs560580170	snp	C/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88660480	AGGCCCAGTGGCTCA[C/T]GCCTGTAATCCTAGT	161436
rs560580613	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88639615	ACAGTCTCACTCTGT[C/T]GCCCAGGGTGGAGTG	161436
rs560606063	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88668550	AAGTAGGGAAAAAAG[C/G]CTAATTGGAGTGGGT	161436
rs560607978	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709151	TTAAACTTCTAGATA[C/T]GGGAATAATAAATAT	161436
rs560627808	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684577	GCCTAATGAAGAGTT[A/T]CAGAGAAAAATAATT	161436
rs560645699	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88741692	TACTGCACTCCAGCA[C/T]GGGCCACATGGTAGG	161436
rs560648293	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789501	GGCAATCCCAGGTGA[A/T]AATAAAATGGTCAAA	161436
rs560682271	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88788615	CCCATAAGGAAAGCA[A/G]AGTCAAATAACAAAA	161436
rs560718648	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88631694	AGAATTGCTTGAACC[C/T]GGGAGGCAGAGGTTG	161436
rs560725400	snp	A/G	1.70156e-05	0.00291677	intron-variant	EML5	GRCh38.p7	14:88646983	AGATAAAGAGGGAAA[A/G]AGATTACAACATAAA	161436
rs560783383	snp	A/T	0.0248432	0.108648	intron-variant	EML5	GRCh38.p7	14:88640154	AGTGTTAGATCATCA[A/T]GGTAGAAAACTAACA	161436
rs560788697	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646286	ATGGGATGTTGATAC[A/G]CAATATGAGGCAGCA	161436
rs560795607	snp	C/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88731772	CATTCTAACTGGTGT[C/G]AGATGGTACCTCATT	161436
rs560827388	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88665980	TATTAAAAAGGAGTC[A/G]AGATACAGATTAAGT	161436
rs560853128	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88751111	GTACTTTCTCTGTAG[A/G]CTTGATAAACATATC	161436
rs560856608	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793179	CCGGGCTCCCGCTGC[C/T]TTGCGTCCTCAACCG	161436
rs560874467	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769137	AGTGGGTGAGGGCAT[C/T]GATATAGTTGGATCT	161436
rs560883577	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88698376	GCTCAAGTGATCCTC[A/C]TTGTCTCAACTTCCC	161436
rs560890548	snp	A/T	0.00557542	0.0525036	intron-variant	EML5	GRCh38.p7	14:88695299	TTCTTTTAATTAAAA[A/T]TTTTTTTAAGTCCAA	161436
rs560898977	snp	A/C	3.67485e-05	0.00428636	intron-variant	EML5	GRCh38.p7	14:88627630	TTTAAAAATCAAACA[A/C]ACAAAAGAATCCTAC	161436
rs560902824	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650849	GTCTTGCTGTGTTAC[C/G]CAGGCTGGTGCTAAA	161436
rs560905437	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88679214	AATACTCTATTTCTA[A/C]ATGAGGACACATTCA	161436
rs560920336	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694592	ACTCTGCTCAAGAGA[A/C]TCTCAAGAGACAGAA	161436
rs560931682	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688845	CCCAAAGTAACTGAA[A/G]TGTCATGCCAACCTC	161436
rs560956397	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88618875	TAAATACTTAAGATC[A/G]GTGACTTTTCCTTTC	161436
rs560956898	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755232	CTGCAATATATTGTG[C/T]GTAAACTTCTCAAGA	161436
rs560976716	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	EML5	GRCh38.p7	14:88794170	AAATAAACTACCATC[A/G]TTTCAAGAAATATGA	161436
rs560995669	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763601	AGCTGGTACCATTCC[C/T]TCCAGAACACTTCCA	161436
rs561009192	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738866	AGTAATAAGACATTT[A/G]TTTTGTTATTACCTT	161436
rs561022141	snp	C/G	1.80742e-05	0.00300612	intron-variant	EML5	GRCh38.p7	14:88681854	GTTAGAAAACTGTGA[C/G]AGCTTAATCTACGTT	161436
rs561040824	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88747120	GCTAAACAAACAAAC[A/C]AAAAAAAAAGGGTCA	161436
rs561041585	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777141	TACTTCAAGGCATTT[A/G]ATAGTCGAACTCCCA	161436
rs561050001	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657649	CAACCAGAAAAAACG[A/G]TGTAGAAGAATATTT	161436
rs561066114	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88649084	GCCCAAGCTGGAGTG[C/T]AGTGATGCCATCACA	161436
rs561111576	snp	A/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613176	TGCTGTGCTGATCCC[A/T]CAGGAAAGGCTTGAA	161436
rs561123927	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644720	TATTCATTTTATTTT[A/T]TTTTTTTTGAGACGG	161436
rs561130518	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693599	CATAAATGCAGCCAA[G/T]AAATGGCAATAAATC	161436
rs561143299	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708430	GACAGCAGTGGTGTC[C/T]TGTTTAATATATATC	161436
rs561152163	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88785895	AAATTATGTCACTAT[C/T]TTGATTAAATAGTTC	161436
rs561209927	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778725	CGGAGGTTGCAGTGA[A/G]CCAAGAATGCGCCAC	161436
rs561227881	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672287	TTGAACAACCTGCTC[C/T]TAAATGACTCCTGGG	161436
rs561258061	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738140	TAAAGCACAATAATG[G/T]TTAGCAAAACTAATG	161436
rs561280161	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88688184	GATAGTCCAGGCAAG[C/T]AGAAAGGCAGTGTTC	161436
rs561293113	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88680053	CTGAAACTTTCTTCA[C/T]TTTATGAAGTATTTA	161436
rs561309364	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88655019	GCATTGATCCCTTTA[A/C]CATTATGTAATGCCC	161436
rs561315361	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737256	GGACTGAAAGAGCTA[C/T]TAACATGCTGTAACA	161436
rs561354086	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88689345	AATGTACACTCCTAC[A/G]AACAGTGAAAAGAAT	161436
rs561354808	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686168	TTGATATTTGAAAAA[C/T]AAGTATGTTGTCAAG	161436
rs561379503	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88633991	CATTAAAAAAAATCC[A/G]CAAGTTTTTTATAGA	161436
rs561391485	snp	C/T			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665407	ATCCTCTAGAGTATC[C/T]GCATTTGCCATTAAG	161436
rs561391958	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88642133	ATCATCAATCTACTC[C/T]TTACCCATTCAGGAT	161436
rs561406716	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88638648	GTGAGAGAAAGGTAC[C/G]TGAAAGCAAATAATA	161436
rs561419921	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756623	AAAATGAAGAGCTAA[C/T]ATGAATTCAGCAAGG	161436
rs561447149	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88744818	CAACCTACCTCTAAA[A/G]GGTTTACATTTTTGG	161436
rs561471700	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645621	ATCTGTTTCTCCATG[A/C]CCTTCACCTTCTCTA	161436
rs561476297	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693142	TTTCAGTTTAGACTA[C/T]AGAACATGTCTTTAA	161436
rs561516408	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669446	CCAGGAGGAATTCAC[C/T]ACAGTGCAGCACAGA	161436
rs561529534	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88686714	TACTCAGGAGGCTGA[A/G]GCAGGAGGACCACTT	161436
rs561534059	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625951	AAAGAGATGTGGATT[C/G]GAAGCCACAGGTCCA	161436
rs561537158	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769400	GAGCCTCCCCAGAAG[C/T]AGAAACTGCTATGCT	161436
rs561547807	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683511	TATTACCCTGATATC[A/C]AAGCCAGACAAAGAT	161436
rs561564059	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715945	CCAAAATAATACAGA[C/T]ATTAGTAACAACCAA	161436
rs561576187	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630184	TACAGGCACCTGCCA[C/T]CATGCCTAGCTAATT	161436
rs561588608	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88734076	ATAGGCAAAGAGTTA[A/G]CATCCATAATATATA	161436
rs561612235	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733635	TAAGGTGTAGCCCCC[A/C]CAGTAAGTTTACAGA	161436
rs561631936	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668938	CCCACCAAGAAGACC[A/G]AAAACGGCAAGTGAA	161436
rs561651082	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740765	TATAGCATAGCTATA[C/T]AGTCACTGGTTTCAA	161436
rs561652595	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88764733	TTTCCCTTGAAACAC[G/T]GCTTTGGCTGAATTT	161436
rs561655757	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88636313	AATCCCCTTGCTCTC[A/C]TGTACACCTTGTTCC	161436
rs561663763	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775380	TGGGGCAGAAGGGAG[C/T]CCATTGCCCTGAAAA	161436
rs561674125	in-del	-/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88660323	GCATTGTATCTGGAC[-/T]TGATATATAAATTTT	161436
rs561676357	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88690229	GGCCATTGTAAGGAC[A/G]GCCTACTTTTGCTTT	161436
rs561681395	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684043	TACAGATGACATAAT[G/T]TTGTACACAGAAAAC	161436
rs561690115	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676637	AAAAAAACTACTTTA[G/T]AATTCATATGGAACC	161436
rs561704774	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88661262	CCTGGCTAATTTTTT[C/T]CTCTGTTTTGTAGAG	161436
rs561709852	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630782	TTTCCCACTGGATAA[C/G]AGCAAGGAAGCACAT	161436
rs561737279	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613620	AAAACATTTGTTGGA[C/T]GACGTGGTTTAAAAT	161436
rs561738053	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766443	TCTTTTACAGTTGTG[A/G]ATAAGGGATGAAATA	161436
rs561742035	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745898	CCTATGTAACAAACC[A/T]GCACGTTCTGCACAT	161436
rs561751352	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88621747	AAGTACAAACACGCT[A/C]AAAAATTTTCATAGG	161436
rs561769262	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734331	TAATGAGTGGTAAAT[A/G]TAAGTATTAGAATGC	161436
rs561821436	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726263	TAGTTGGGACCCAAA[C/T]TTTATAGCTCAAAAT	161436
rs561833163	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88759262	AGTTAGACAGACATG[C/G]GTTCAAAATTCTGGC	161436
rs561888775	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766864	TTTCTCAGACTGGCC[A/G]ACACTTAGGGAAAAT	161436
rs561889020	in-del	-/AGAA	0.00120216	0.0244875	intron-variant	EML5	GRCh38.p7	14:88699321	TACAAAGAGGCAAAT[-/AGAA]AGAGATAAAAAGGGG	161436
rs561901476	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88748645	CACTCAATAGAAACA[G/T]ACTCAGGAAACCCAG	161436
rs561914898	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88713513	GCCACGATCTTGCTC[C/T]TTCACCCAGGCTGGA	161436
rs561918860	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88736874	TGCTTTTTTTAAGCC[-/T]TTTTTTTACTCACAA	161436
rs561923319	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773448	GGTCCCAGTACTTAC[C/T]CACATTGTCATATAA	161436
rs561938460	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720308	AGCAACATCTTGATA[C/T]CAAAACCTGGCAGAG	161436
rs561970244	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727708	CAGCCAATACAATGC[A/G]TTTTTAAACAATGCA	161436
rs561976632	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718318	GCGTGGTAACTGACA[C/G]CAGAGGCAGAATGAG	161436
rs561986221	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88692760	ATGTAAAAATACTTC[G/T]TTTTACTTTGTAAAC	161436
rs562036966	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88747854	TGGACTTCTAGCCAT[A/G]AAGGAGTATCAAGGT	161436
rs562043276	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88652482	TCAAATCCCTCTGAC[A/G]AAGCTTTCCTGTAGT	161436
rs562144641	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674638	CTGACCCTGGCACTT[C/G]CCAAATTTCATGTCC	161436
rs562146058	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617586	CCAGCCTGGGCAATA[C/T]TGTGAGATCCCTATC	161436
rs562165412	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88659275	GGAATGCAGTGGCAC[C/G]ATCTTGGCCCACTGT	161436
rs562184799	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88657217	AGGCTGATACCAAAA[G/T]GTATTTAAAGACAGA	161436
rs562196395	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666726	ATAAACACAAAAAAG[C/G]GCTTACCCTAACAGC	161436
rs562201928	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88708641	TAATGCACAGAAGAG[A/G]GCAAAAGTTTGATGT	161436
rs562213346	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88722638	AGGGGAGGGGGAGCA[G/T]TAGGAAAAATAGCTA	161436
rs562215000	in-del	-/TTTTTAAAACATTCTGAATTAAG	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88716924	TGAAAATTTGTTAAT[-/TTTTTAAAACATTCTGAATTAAG]TCTCTGGGAGACTAA	161436
rs562250935	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770829	TATATTCCCATTCTA[A/G]AACATTTAACAAGAT	161436
rs562254760	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88682575	CTCCTCATCTGGTTG[C/G]AAACTCCGAGACTGA	161436
rs562258041	in-del	-/CTA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88707863	TCAAGAGGGCTTTGG[-/CTA]CTACTACTACCTTTG	161436
rs562265181	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88629412	TAAAACGTATAGGTA[C/T]GTAAGGTAATGGAAT	161436
rs562265815	in-del	-/AAATGTGGGGTTGGAGCCCCCACACAC	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88783199	GGAAGTGCATAAAGG[-/AAATGTGGGGTTGGAGCCCCCACACAC]AAATGTGGGGTTGGA	161436
rs562287818	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88696437	ATATGTCTAAAATAA[A/G]TATTTCAATTCTCAA	161436
rs562289868	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704197	GATGAGTGAGTTCTC[C/T]CTTGATTAGTTCATA	161436
rs562327553	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88703320	GTAACTATCTGCAGA[A/G]AGGGGAAATGATGGC	161436
rs562343974	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88653090	TTCACTCATGATTTG[G/T]CTGTTTGTCTATTAT	161436
rs562364753	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88711525	AAACCATTGGATCTC[A/G]TGAGAATTCACTCAC	161436
rs562367900	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642302	ACATTGTTCATGAAA[C/T]GATGCTAACAGAACA	161436
rs562401263	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88660303	AAAAAAAAAAAGAAA[A/G]GAATGCATTGTATCT	161436
rs562418085	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714317	AATCTGTTTTAGATC[A/C]TCCAGCCAAAGCAGT	161436
rs562422231	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88620266	CTGTTGAAAAATGCT[G/T]AAGCACTGAAAAACA	161436
rs562423621	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88744976	ATGAAAAACATATCA[A/G]TGCAACTTTGAAATA	161436
rs562433291	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664245	TTGTACCACAGCATT[C/T]CAGCCTGGGTGACAG	161436
rs562435640	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88754112	GCCTGGGCAGCAGAG[C/T]GTGACCCTGTCTCTA	161436
rs562478108	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767500	ATACTTCCCACAACT[A/G]GGCCTGCCTCTGGAC	161436
rs562526245	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88691578	CCTCTGTCCCTACCA[C/T]GAATAGAGTTCAAAT	161436
rs562528038	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698883	AGCACCTTACGAACA[C/T]TGACTCATGTACCAA	161436
rs562541752	snp	C/T	1.74318e-05	0.00295222	intron-variant	EML5	GRCh38.p7	14:88714889	CTTCCAGTAAAACTC[C/T]AAAATATTGTATAGG	161436
rs562546000	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88617041	TGAATTTCATCAGGA[-/T]TATCAACTCCTGCCT	161436
rs562550464	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88671531	GCATCACGATGACAG[A/G]ATCAAATTCACACAT	161436
rs562577596	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88649812	TTTGTTGACAAATGT[A/G]GTTAAATGTTTTATA	161436
rs562600644	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768110	TTCTCATGATTAAAG[C/T]GGGGTTATGCATTTT	161436
rs562601776	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760514	CTGTATTTTACACCA[C/T]TAACCTATGTATCTA	161436
rs562603606	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708224	TTTTAATAACTTGTT[C/T]TGATAAATGGGTATC	161436
rs562613937	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670429	AGCAGCCTCAAAGAC[C/T]GAAGCTAGATAAACT	161436
rs562656869	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693659	CAGTAAATTACTTTT[A/T]AAAAATAAACTAATT	161436
rs562660620	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88762443	TGAACCCGGGAGGCA[A/G]AGGTTGCAGTGAGCT	161436
rs562688772	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792109	CTGCACGGACCCGAG[A/G]GAGAGTCCCTAGACG	161436
rs562726153	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88788733	CAAAAATTTGCTTAC[A/G]GGAAGTACCTAGAAT	161436
rs562726782	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758025	ACCTGTCTAATTTTT[C/T]TTTTTTTTTTTTGTA	161436
rs562760585	in-del	-/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88700101	TAATGCTTTTGAATA[-/G]GAAGCACTCAACAAG	161436
rs562786241	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88729558	GCATATACTTATTTG[A/G]TTTTTTGTTTTTTGT	161436
rs562791178	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649122	GCAGCCTCAAACTCC[C/T]AGGCTCAAGAGACCC	161436
rs562803770	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656596	CGTTCTGCACATGTA[C/T]CCCAGAACTTAAAGT	161436
rs562851335	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653894	TCTTTGTACTTCTGG[C/T]AGAATTCGGATGCGA	161436
rs562890424	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88692146	TTGGGAGGCCAAGGC[A/G]GGTTGATCACCTGGA	161436
rs562908131	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88692815	TTTGATAAAGTGTTA[A/T]ATCCAAGACTGAAAA	161436
rs562909148	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770164	GGTATTCTCTGTTTA[A/G]GTAATGCTGGGGCTA	161436
rs562931123	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696169	CAACTCTTTGAATAT[A/G]TATATATATATATAT	161436
rs562942985	in-del	-/GTAA			intron-variant	EML5	GRCh38.p7	14:88696513	TCTGGCTATAAAACG[-/GTAA]GTGAGATCAGTGCCC	161436
rs562943243	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661578	ACAATTAATAACAAT[A/G]AAGTGCTATGACAGG	161436
rs562997395	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654846	CCTTGTTAATTTTCT[G/T]TCTCGTTGATCTAAT	161436
rs563007625	in-del	-/TTTTTG	0.00517822	0.0506191	intron-variant	EML5	GRCh38.p7	14:88624071	TATATGTCACATTTT[-/TTTTTG]TTTTTGTTTTTGTTT	161436
rs563045097	in-del	-/AAC	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88687779	ACAAAAAAAACACAA[-/AAC]AACAACAGCAGACCT	161436
rs563074164	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624258	ATTGTTGTTTTTTAT[A/G]GCGATGGGGTTTCAC	161436
rs563083338	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781760	TGCCACCATGTGAAG[A/G]AGGACATGTTTGCTT	161436
rs563114393	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685303	ATTAACCTCAATCAT[G/T]CAATTTAGTAATCTC	161436
rs563133855	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88718482	AACAGAAAGAGAAGA[A/G]ACACCTAAAAGCCAA	161436
rs563138256	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88640773	ACAAAATAAAAAAAT[C/T]GGTTTTTTGAAAAGA	161436
rs563179865	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735838	ATATTATATTCCTGT[C/T]AAAAAGGAGGAGGTA	161436
rs563197620	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88647994	TCTGACCTAAGAGGG[C/T]TCCCCAGTCAGTGAA	161436
rs563198727	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702285	TAAAACTGTAGGAAA[A/C]AAGTTTGGGGTAAAT	161436
rs563199781	snp	A/C	0.0287284	0.116357	intron-variant	EML5	GRCh38.p7	14:88640162	ATCATCAAGGTAGAA[A/C]ACTAACAAAGAAATT	161436
rs563201174	snp	C/G	0.000264975	0.0115073	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621278	GATTATTTCAGCATT[C/G]CTTGTCCCAACAAGG	161436
rs563216600	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743536	CCTTATTTAATCATC[A/T]ATTCTTTGAGGATGG	161436
rs563240972	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639857	AAATGCTGGGATTAC[A/G]GGCATGAGCCACCGT	161436
rs563277094	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785323	TACATTTTAGAATAA[C/T]TAAAAGGTTGCAACT	161436
rs563283971	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88742117	TGGACTCCCAATTGA[C/G]ATGAACTGAGACAGA	161436
rs563291082	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88674838	GGGGTACAGGCATTG[A/G]ATAATACAGCTGTCC	161436
rs563291398	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689516	TTACCTATTGATATC[A/T]CTTGCCCATTTTTCC	161436
rs563316901	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794264	CTTCCTCAAAGATGC[C/T]AGTTACTAACTTGAG	161436
rs563317423	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776091	TAAAGCAGATACAGC[C/T]TAGATCACAACACCC	161436
rs563337700	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710644	AAAAATGCAGTAGTC[A/G]TATTCTGTCTTTCCC	161436
rs563353090	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88682621	TAGGCTCTCTCTCCC[C/G]CCAGCTCGCGGTCAG	161436
rs563354411	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775560	AGAGTGGGAAGGACT[A/G]CGCCTTGTGGTTTGA	161436
rs563360478	snp	A/G	0.0154538	0.0865337	intron-variant	EML5	GRCh38.p7	14:88695665	GTATCTGCTCTCATC[A/G]CACCTGATCTCCTTT	161436
rs563367206	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726466	TTATATATTCTGTAT[C/T]GCTGAAGAGAAAATT	161436
rs563374413	in-del	-/A			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680315	ACCATATCTCAGGAG[-/A]AAAAAAACAGAGAAA	161436
rs563375442	snp	A/T	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88628952	ATAAAATAGGTTATT[A/T]ATGTTTGTAAAATTT	161436
rs563376975	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88662208	GAAATTTAGAACTTT[C/T]ACTTATGGTCTCTCC	161436
rs563397469	in-del	-/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88752395	TTATGCTATGAAATA[-/G]GTATTATTTCCTTTA	161436
rs563454003	snp	A/C			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612890	GGTGTATAGTGTTAA[A/C]AATTAAAGCTTAAAA	161436
rs563465327	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643218	CAGCTTAAACATACA[A/T]TCTATACTTTTCTAT	161436
rs563471624	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88724790	TTTATTATTTCTAAC[C/T]TGCAAAACTGAAGAG	161436
rs563479744	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777995	ATACAGCAAATTTTT[A/T]AAAATGAGGGGACCA	161436
rs563480446	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88786035	GTTCACTCTGCTCCA[C/G]CCACACTAACATTCT	161436
rs563489478	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88680953	GAAAACATCCAAAAG[A/G]ATGGTAAGAAAAACA	161436
rs563540879	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643034	GGTCCTATAATGATA[A/G]TAATAAAACCATTAT	161436
rs563549349	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88627967	CTCAAAACTAAGGCT[A/T]AATTTAAGAAAGGAA	161436
rs563576426	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731136	CAGGTTTGTCACATA[G/T]GTATACATGCGCCAT	161436
rs563605221	in-del	-/GC	0.00557542	0.0525036	upstream-variant-2KB	EML5	GRCh38.p7	14:88792878	CCCCGGTCACCTGCG[-/GC]GCTCGCGCCCCGCCG	161436
rs563606233	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731871	ATAAATGTCTTCTTT[C/T]GAGAAGTGTCTGTTC	161436
rs563611636	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686531	CCTCTTCAAAAAAAA[A/G]AAGGTAGGCCAAGCA	161436
rs563612913	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88737901	TTTTCCTTTTAATAA[A/T]CTTTTTACTTGTCTA	161436
rs563614517	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645118	TGCAACTCCACCTCC[C/T]GGGTTCAAGCAACTC	161436
rs563620100	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666072	CAAAAGCAAGTATGG[A/G]TATTTACCTTAAAAG	161436
rs563675603	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88618911	CTTAAAAGTAACGTG[G/T]GATAAGGCCTCAAAT	161436
rs563679163	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672829	TACACTCTCCAAAGA[C/T]GGAACCAGGAAGAAG	161436
rs563679845	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88792931	GCGGACCCGCGCCGC[A/G]CACCCCGAAACCGAG	161436
rs563711904	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773523	TTTCAGGTTGACTCC[C/T]AGGCCAGCACCTGAA	161436
rs563718232	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680210	TTTGACTCATGAATA[C/T]CTTAAGAAATAAAAT	161436
rs563729229	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709988	ATTTTCATTTGTCAA[C/G]AAGAAGTACAGAGGG	161436
rs563763382	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751337	AGAGAGAGTCAGAGA[C/G/T]AGTTTGTAGAAAAGT	161436
rs563765829	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717627	AGGTGTGGTGGCATC[C/T]GCCTGTAATCCCAGC	161436
rs563785775	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730746	GAATATATTCAAAAT[A/C]ATTGAGAAAACACTA	161436
rs563788947	snp	C/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88640148	ACTGATAGTGTTAGA[C/T]CATCAAGGTAGAAAA	161436
rs563792276	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619396	AAAATTTAATTTTTT[A/T]AATAGAGGCGGGGTC	161436
rs563817032	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654681	CTTTTGCATTTGCTG[A/G]GGAGTGTTTTACTTC	161436
rs563833312	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88687110	AATTCTGATGCCCAA[C/T]AAGACGGAAAAATAC	161436
rs563854237	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639519	TTTTCCATTTAATAA[C/T]TTGGGCCATATTGAG	161436
rs563869530	snp	A/G	1.65723e-05	0.00287852	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658278	TGTCCACACCATTAA[A/G]GACATATCTGTACCG	161436
rs563879203	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668972	TGCACCAGCAACTGA[A/G]GTATCCAGGTTCTCT	161436
rs563901222	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663131	TTTCCTTCAAAAAAA[A/T]TTTTAAAAATATTTA	161436
rs563904260	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88701460	TATTTATCTTTATAT[G/T]CCTAGCACATTTCTT	161436
rs563906272	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88714496	GTACAGTTAATAATG[C/T]TGTTACTGTATGATA	161436
rs563907671	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88655025	ATCCCTTTACCATTA[C/T]GTAATGCCCTTCTTT	161436
rs563928077	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88730849	AGAAAAAATGGCTTA[A/C]AGAAATTTACACAGA	161436
rs563938083	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676755	AAGGCTACAGTAACC[A/G]AAACATCATGGCCAC	161436
rs563950260	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88617440	GCTGAGCCACCGCGC[A/C]TGACTGAAAACTGAT	161436
rs563967637	snp	C/T	6.05467e-05	0.00550179	intron-variant	EML5	GRCh38.p7	14:88696822	GCATTTTGTTAATTC[C/T]TACTGAGACAGCAAA	161436
rs563980559	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724596	ACTACTTTTGAATGT[A/G]TATCAGATATGATAG	161436
rs564037404	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767362	TCAACTATACCCTTA[C/T]GAAGATGCCCTTCTT	161436
rs564042691	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770072	CTCAGCAGCAGAGGA[A/G]AGGAAAGAGCGCTTG	161436
rs564062358	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88721173	AAGAATGAGTATCAT[C/G]AAAATTGCCATCCTG	161436
rs564063032	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677328	TAAAGACTTAAATGT[A/G]AAACCCAAAACTATA	161436
rs564072773	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779856	TACATTGTGAGTTCA[C/T]ATGGACATTTCCAAT	161436
rs564076185	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766923	GCTGGTTTCCCCCGA[G/T]AGCACACAGTTATAA	161436
rs564095599	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788732	GCAAAAATTTGCTTA[C/T]GGGAAGTACCTAGAA	161436
rs564101095	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720455	GGAGGCTTCATCCCC[A/G]AGATGCAAGGCTGGT	161436
rs564102145	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698540	AAAGTGCTAGGATTA[C/G/T]AGGCATGAGCCACGG	161436
rs564115944	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780584	AAATCTTTTTTTTTT[C/T]CTTTTAAGATGGAGT	161436
rs564136488	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728612	TCATCTTCACATTGT[G/T]TAGGCTGAGGAGGAG	161436
rs564141095	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705616	AAAATGAAATGTTAC[C/T]TGTTTAAAGAAGATT	161436
rs564176662	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735035	TGTGGTGATGTTTGA[C/G]ATATCTTTTAAAGAT	161436
rs564213177	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719247	AACATTAGCTAGGCA[C/T]GGTGGCTACTTCCAA	161436
rs564224708	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669837	TTATACAGGGGCGTT[G/T]CCACTGGTATCAGTT	161436
rs564267149	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88761205	AGGATGTTGTTTTTT[A/T]AAAATTATTATTATT	161436
rs564281797	snp	A/T	0.00607897	0.0547954	intron-variant	EML5	GRCh38.p7	14:88758200	TATATATGTGTATTT[A/T]TTTTTTTTTGACACA	161436
rs564286202	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88725831	GGAAGGAGATTAATA[G/T]GAGAGCTATCTCAGA	161436
rs564289092	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88664343	GTATTCATCTTCAGA[C/T]GTAAAATAGTAAAAA	161436
rs564301180	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88690352	TACAAGGGAGGTCAA[A/G]GATGAAAGGAGTTAG	161436
rs564321594	in-del	-/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88773174	AGTCTGCTGAAATCA[-/T]CACCTGAGGCACTGG	161436
rs564325237	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713666	CTCACCATGTTCCCT[C/G]GCTGTTCTCAAACTC	161436
rs564325597	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721729	ATTTCATGAAGAAAT[C/T]GCTAAAAGCAGCTGC	161436
rs564350610	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88734820	CAAATCCAGAATGTG[A/G]GAAACGCTGAATAAA	161436
rs564365855	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88632488	GCATCCTGCATGAGA[A/T]GACCACTATCCCTCT	161436
rs564366754	snp	A/G	8.15228e-05	0.00638395	intron-variant	EML5	GRCh38.p7	14:88638772	TTGAACAAAGCAAAT[A/G]CTTTAAATTGTTTCT	161436
rs564418768	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740804	TGTAAGAATAAGGGG[A/T]TTGAATCAGATTATT	161436
rs564442502	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669528	AACCCCTCACTGTGC[A/G]GGGCCTCCCTGCAGG	161436
rs564442772	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660383	TTACAGTAGTTTGAA[C/T]AGAGGGAAGTGATAA	161436
rs564506484	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614570	TTAACACATTAAAAA[C/G]TCATAGGGTCAATAC	161436
rs564506645	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787904	AAACGGCTTGTGTTA[A/G]GAATTCTAGGCATGG	161436
rs564516356	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88709008	TATTTGTGTTTCAAT[A/G]ATTCCATTTCTTTTA	161436
rs564547584	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660072	CCTGGGTTCAGGAGT[C/T]TGAGACCAGCATAGG	161436
rs564553160	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708339	GATTACCCCTTGTGA[C/T]TATATTTATATAACA	161436
rs564553824	in-del	-/GTT			intron-variant	EML5	GRCh38.p7	14:88719853	TTAATCTAGGATCTG[-/GTT]TTTTGAAAAAATTAA	161436
rs564556545	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710974	ATTCACTTGACTAAG[A/G]AAACTAAGAAGATTA	161436
rs564593538	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715840	GCTAATCTTTTTGAC[A/G]TTTTTAAATAGAACA	161436
rs564602279	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772446	AACCATCTAAGATGG[C/T]ACTTTCAAGCCTTTG	161436
rs564612926	snp	C/T	0.00914312	0.0669923	intron-variant	EML5	GRCh38.p7	14:88638539	TGCTGACCAGAAATT[C/T]CTGCTAAAGGACTAA	161436
rs564613464	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726930	TTGGAGTGCAGTGGC[A/G]TGATCATAGCTTACT	161436
rs564727034	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697864	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	161436
rs564761258	snp	A/G	6.64982e-05	0.00576582	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704900	TATTTCCTGGAGCCC[A/G]CTCTCTTCTTTTAGA	161436
rs564764019	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88627544	AGGCCTCCACTGAAT[C/G]ATTGTTTCAACCACC	161436
rs564775009	snp	G/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88661079	TTGAAGTTAATATTG[G/T]GGATAAAAGGAATGT	161436
rs564777961	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738060	CCAATATAAAGACAC[C/T]GTGTACCTCACAATG	161436
rs564789970	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653725	GAGGACTTTCACATC[A/G]ATGTTTACCAGGCAT	161436
rs564807480	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652282	CATGAGGTATACCAT[C/T]AGCAAACGACACCTG	161436
rs564831317	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763516	AGGCAGTAATTAATA[A/G]CCTACCAACCAAAAA	161436
rs564853242	in-del	-/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88747237	GGCAACACGTTGAAA[-/C]CCCGTCTCTACTAAA	161436
rs564869809	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672187	ACAAAAGAACTGAAA[C/T]CATAACAGTCTCTCA	161436
rs564909205	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88718680	ATAGAGGTTGATAAT[C/T]AGAAGAAAAGAGAGA	161436
rs564924230	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692989	TTGATGTCACATTGA[A/T]GGAATTTATAAGTAT	161436
rs564953546	in-del	-/CAGA	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88736624	GATAGCAGCAGGAGG[-/CAGA]CAGACAAATCCCTAT	161436
rs564987900	snp	A/G			intron-variant, utr-variant-3-prime, stop-gained	EML5	GRCh38.p7	14:88616113	CTAGTAACATAGTCT[A/G]CTCTTCATGGGCTGA	161436
rs564992823	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88784173	AGGGAAGTTTAAAGT[G/T]GTAAGTGCCTACATC	161436
rs565008608	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88769327	TCGCTTCCTTCTACT[C/G]TAGCCATGTGAAGTG	161436
rs565012828	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664350	TCTTCAGATGTAAAA[C/T]AGTAAAAAATAATTT	161436
rs565027349	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88650757	AATCCTCCTGCTCAG[C/T]CTCCTGAGTAGGAAC	161436
rs565037069	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88688116	TGTGTTCGGGAGTTT[C/G]AAAAGAGAAACAAAG	161436
rs565073916	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701171	GGTGATTTTGCCTTC[A/C]AAGGGACATCTGGGT	161436
rs565091455	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88728584	TGGATCATCATAAAA[A/G]TCTACATCCTCATCA	161436
rs565093640	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88793063	AGTTCGCGGGGCCAC[A/G]GTCTAGTTGCGGAGT	161436
rs565112126	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88782119	GGCTTTGTCTAAAAT[C/G]ATGATAGTGATATGG	161436
rs565125192	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756804	ACACTGAAAACTACA[A/G]AAACCCACTGAAGGA	161436
rs565125953	snp	C/T	3.32082e-05	0.00407468	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714981	CATTTCCATCATTTG[C/T]CTGCAAATATCTACT	161436
rs565130630	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792139	GAGGAAGAGGGGAAA[C/G]GCATTTGTAGGGTGT	161436
rs565139755	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755047	TGACCTCAAGTGATC[C/T]GCCTGCCTCAGCTTC	161436
rs565153584	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789936	ATGAAAACAGCACTG[A/C]CTTTTTATTACTAAA	161436
rs565159214	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88699665	ATTGTCAGTAGAGAT[A/G]TGGAAAAATTAAAGA	161436
rs565183337	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657986	GATATTTTTCATTTG[C/T]AGATAAATAATATCA	161436
rs565205731	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765473	CGGCACATTGAGTTC[C/T]TCTCAAGCTTTGAAT	161436
rs565262123	snp	A/C	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88686047	ATACAGTGAGGAAAA[A/C]AGACCCTGTGTTAGG	161436
rs565265126	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790914	CCCTAATCACCACGA[C/T]ACAGAGTCCCAGCTT	161436
rs565286138	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679808	TATCTGATGATACAA[C/G]AGTCACAGGAAATTT	161436
rs565306049	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88722399	ACTGGATAAAGAAAA[G/T]GTGGTACATGTATAC	161436
rs565307934	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612083	TAGTCATGGTACTGC[A/G]GCTTAGGGGGCTACA	161436
rs565331024	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723393	GCTTATATGTGGAAT[A/C]TAAAAAAGTCAAACA	161436
rs565359955	snp	A/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88682139	TATATGATAATAGGA[A/T]ACCGAATAGTGAGTA	161436
rs565367639	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730579	ATTAATTTAAAAACA[A/C]GACAAATAATTTTGA	161436
rs565379257	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659122	TACATAAATTTCAGA[C/T]CAAAGCATCATAAAG	161436
rs565382064	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88661341	AGTGATCCTCCCACC[C/T]CAGGCTCCCAAAGTA	161436
rs565401363	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629592	ATTCCTGATGCTTGG[C/G]TAACACATAAACAAT	161436
rs565417161	snp	A/T	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88698989	TAGGTAATTTGCCAG[A/T]AGCGAATAAGTGGAA	161436
rs565438347	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88633774	GCTTATACTTTTATT[A/T]AAGTGCTTAAAACAG	161436
rs565451447	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768217	GATGATGTTTACCTC[A/G]ATCCCTTGGTTAAAC	161436
rs565462312	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617610	CCCTATCTCTACAAA[A/T]ATAAAAATGACTTAT	161436
rs565471609	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88681381	TTTGGCAGGCCGAGG[G/T]GGGCAGATCATGAGG	161436
rs565477907	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689039	ACCAATGATTTGTTA[C/T]AGAGTTTTTTACATG	161436
rs565487589	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774843	ATACCAGCTCAGATT[A/G]CTTCCCTGAATTATA	161436
rs565501003	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674123	AAAGTACAAAAATTA[G/T]CCAGGCATGGTAGCG	161436
rs565526180	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625409	CTAGGGTTTATTTTT[A/T]ATTTTTTTGAGACGG	161436
rs565529393	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88703632	TTTTTCAAATTCTTG[A/G]TAAGTATTATCAGTC	161436
rs565531628	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633899	TACAGGTGTGAGCTA[C/G]CATGCTTGTCCAAAA	161436
rs565558707	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777493	AATCCCAAGTGGGTT[G/T]TGAAGGTACAAAACT	161436
rs565562823	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88743887	TTTGACTGAACATAA[A/G]AACAATAAAAACATT	161436
rs565583881	in-del	-/AG	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88623444	TTATTTTTTTGAGAC[-/AG]AGTGTCGCTCTGTCA	161436
rs565593796	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632907	GATTTGACTGCTGGA[A/G]GAAGAAGCAGGTTCT	161436
rs565655062	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771219	TTCTCAACCTCCAAA[C/T]TCTCACATGAGCACA	161436
rs565702543	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757674	GGATTTTAACAGACA[C/T]ACCCCCAAGGAAGAT	161436
rs565707246	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657817	TGTTACCTCTGTGTG[C/G]TCAAATTATGGAGGC	161436
rs565710226	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628153	ATACTTTTAATCTTT[A/G]TACAATTATATGGAG	161436
rs565719897	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776842	GCTGAGATTATACTG[C/T]TGCACTCCAGCATGG	161436
rs565739273	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88763172	TCACAGCAGAACTGA[A/G]GGAGACAGAGAAGAA	161436
rs565756811	snp	A/G	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88732052	TTTCTTTTGCTGTGC[A/G]GAAGCTCTTTAGTTT	161436
rs565794050	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613039	AATGATGATAAACCT[A/G]CATGTGCAAAGGCTC	161436
rs565803827	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731316	TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTGT	161436
rs565805536	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88739324	TTGTGGGATGCAAAA[C/T]CCATAGATAGGGAGG	161436
rs565822634	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88678298	TTGGGGGACAGGGAG[C/G]AGGGAGAGCATTGGG	161436
rs565835465	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88640982	TAGTTGTGGGCCTCT[-/A]AAAAAAAGAAGAAGA	161436
rs565838984	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88717832	TCAAAACCAATTAAA[A/G]GGTTACTGCAGATGA	161436
rs565841705	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88645531	ATCCTTCTTGAAAGT[A/G]AATTTTCGTAATATT	161436
rs565852459	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88660122	CTCTACAAAAAAAAA[A/T]TTTTTTTTACATTAG	161436
rs565864094	in-del	-/TTG/TTTG			intron-variant	EML5	GRCh38.p7	14:88729871	GGTCTTGTTTTTTGT[-/TTG/TTTG]TTTTTTTTTTTGTTT	161436
rs565884402	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667050	ATGTGGGGTGAAAGG[C/T]GTCAAGGGCATGGTT	161436
rs565931701	snp	C/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88718654	AAAGCAGAAGGCATA[C/T]AGGAATGAGGATAGA	161436
rs565951531	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667758	TGGCATTCACCAGAG[C/T]GGCAGCCCCAACTGC	161436
rs565993545	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88786873	GTATCTCTTTATCAG[A/C]AGCATGAAAACGGAC	161436
rs565997329	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618978	GAGATTGTCTGGGTT[A/T]CATGAAATAAGGAAG	161436
rs566017632	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772110	TAAATGATATCACCA[C/T]CCATTCAATTGCTCA	161436
rs566017855	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88764549	TTTTCAAAGAACCAA[C/T]TTTAGGTTTTTCTCT	161436
rs566041388	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650381	ATCATTTGAACCCAG[A/G]AGTTGGAGGTTGTAG	161436
rs566042936	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723930	ATTCTAATTCATTCT[A/G]TTTTCTTCCAACTCT	161436
rs566072780	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709568	CATTTACACCAACTG[G/T]GTTTGCAAAAGTTAG	161436
rs566106639	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654119	ATTTCTGTGCAATCA[G/T]TGGTGATATCCTCTT	161436
rs566129281	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88675052	GAGTATAGCCCCCTT[C/T]CTGGCTGCTTTCACA	161436
rs566147281	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88755883	ATACACCTCTATTCC[C/G]AGCTACTTGAGGGGC	161436
rs566174199	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644197	GTTTAGGACTCCTCT[C/G]AGATACAGTTCAATT	161436
rs566183141	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715689	TTGAGACAGAGTCTC[A/G]CTCTGTTGCTTAGGC	161436
rs566183848	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719741	AAAAGGACTTTCCAA[C/T]GCTACTCCCCTTGCA	161436
rs566184672	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88617997	TATCTTTAAAGTTAA[A/C]ACTTTGATTTCCTTA	161436
rs566210945	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88681174	TTAAAAAACAGATGG[C/G]AATGAACTGCTATAA	161436
rs566231147	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746834	AACAAATAACCCCTT[C/T]CTAAAGAAGCGGAGG	161436
rs566239921	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738510	ACAAAAGTTTCCCAA[A/C]CCTCAATATTTACCC	161436
rs566243445	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88695572	AAAATAATGTTAAAT[G/T]TTAGGCATGCATACA	161436
rs566244548	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644192	CTTAGGTTTAGGACT[C/T]CTCTGAGATACAGTT	161436
rs566310537	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750842	AGCAAAAATCTAGCT[A/G]GAACAAATGTATCTA	161436
rs566316818	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88733162	CACAAATCTGCAGCA[A/G]ATATTTTTTGGAGCT	161436
rs566318856	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662537	GCCGTGCAAGTGATT[C/T]ATTCCTTTTTTTTTT	161436
rs566321167	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781146	CCCTGTGGGTTTAGG[C/T]GGGCAAAGATGACTG	161436
rs566323376	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88723293	GGAAGAAAATCCTGT[A/C]ATTTGCTACCACACG	161436
rs566323598	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88684883	GTATACATTAAATTT[C/T]TTTTCTGTATACATT	161436
rs566327051	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88782855	GAGGCTGAGGTGGGT[A/G]GATCACCTGAGGTCA	161436
rs566339658	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698075	TAACAAATAACACTG[C/T]AATCAGCCAATATTT	161436
rs566372635	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713733	AGTGCTGGGATTACA[A/G]GCGTGAGGCACTGCA	161436
rs566427261	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88685914	GTTGGTTGAATCTGA[A/G]GATATGGAACCCACA	161436
rs566435503	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655243	TACTACAATGCTACA[A/G]TAACCAAAACAGCAT	161436
rs566467066	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705659	AGCACTGAAAAATTA[A/C]TGATTAAGAGCTATG	161436
rs566506433	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705214	TTTTTATACTTCATA[A/G]AAGAATATTGTTAAA	161436
rs566508041	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743825	TTAATTTCCTATTCA[C/T]ACCTATATTCCTTAC	161436
rs566528896	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615455	CATTTTGCTAAAAAG[A/C]TAATGAAAATTATCC	161436
rs566544563	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88713143	ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCCG	161436
rs566549563	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88769906	TAGACACAAAGACAG[G/T]TCAGAATTGGTAGCC	161436
rs566572128	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720539	GACCATATGATTATC[C/T]TAATAGGTGCAGAAA	161436
rs566578042	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690378	GTTAGAAGGCTATTT[C/T]AATCATCTGGGCAAA	161436
rs566623060	snp	C/T	3.37593e-05	0.00410834	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740409	GCTCCTTGTATTGTT[C/T]GTATAAGATTGATTC	161436
rs566630977	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88735459	AAACATATAAAAACA[G/T]AACAACCCTCAATAT	161436
rs566653058	in-del	-/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88774841	CTATACCAGCTCAGA[-/T]TGCTTCCCTGAATTA	161436
rs566684029	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88727350	AAGGGATGTGAGTAT[A/G]CCATCTCTTTCCCAA	161436
rs566705081	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88623354	AGATGTAAAAAAACA[A/G]TTTTATTAAAAGGAT	161436
rs566728062	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698631	AAATACAAACCTCTC[C/T]CAAGGTGGTCTTTAA	161436
rs566785889	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751588	TAGAAAATGGAATAT[C/T]TACAGAACATTCAAG	161436
rs566815497	in-del	-/AATG	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88661934	GTGTGTCACAAGTAA[-/AATG]AAAGTTTTAATGAAA	161436
rs566837109	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690371	GAAAGGAGTTAGAAG[A/G]CTATTTCAATCATCT	161436
rs566845803	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645485	TCTAAAGTATCTAAC[A/G]GAGTATCTTCACATG	161436
rs566878967	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88748049	CTAGGAGGCAATTTC[C/T]AGACCATGGCACAGA	161436
rs566931468	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88658717	GATCTATGCTAAGAA[A/T]TGCTATCTGTGTAAA	161436
rs566932552	snp	A/C	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614882	AGAAAAAAGGCTATA[A/C]AAATTTTATTCCAAG	161436
rs566944830	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749329	CACAGAATTGTATAC[G/T]AAGCAAAAATATCCT	161436
rs566966522	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653336	TCCAACAATATGTTG[A/T]ATCAAAGTAGTGAGA	161436
rs566969676	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772684	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	161436
rs566978421	snp	C/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88652576	GAATTTTCTACAAAT[C/G]CTGTTCAACTGTGAA	161436
rs566981835	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700683	ACTCAGAGGTGGAAT[A/G]AGGCAAATACCCACA	161436
rs567004489	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779241	ACTGATTAAAGCCTT[C/G]TTCTAATATCTTTTT	161436
rs567028259	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88676890	GCAATGGGGAGAGGA[C/T]TTCCTATTTATTTGT	161436
rs567066547	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779956	TGTTTCTGAAAAAAA[A/T]TTTTTTTTTTTGAAA	161436
rs567086837	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88728098	ATGCATATACAGTTG[C/G]CCCTCTGTATCCATG	161436
rs567110031	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88737569	GTAGCACCCAAAATA[C/T]CCTGTGTCAATAATT	161436
rs567121349	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787988	GATTCCTGGGCTCCA[A/G]CCCTAGAAGATTCTG	161436
rs567144563	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687438	ATAGTCAAAAGTTAC[A/C]GCTTGTAAAGAACAG	161436
rs567172352	snp	C/T	9.26569e-05	0.00680587	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638889	TCATCATTATGTTCC[C/T]GATAAAAACTCTGAG	161436
rs567172927	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724963	CGTAGTCTTTCATCT[C/G]TCTTCAAGAAGCTGT	161436
rs567204489	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683777	AAATGCTCCACAAAT[A/T]TGGAATAAAAGGGTA	161436
rs567205867	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88724157	GCACGCACCTATAGT[C/T]CCAGCTACTCAGGAG	161436
rs567209800	snp	A/T	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88731196	TTTACATTAGGTATA[A/T]CTCCTAATGTTATCC	161436
rs567241908	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745558	ACGTAATTTTAAATC[C/G]ACACAAGCAACATTA	161436
rs567244475	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730915	TTCATTGTATTATTC[C/T]TTAGCACGTACTTAG	161436
rs567265615	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88678744	TCACAGAGATAATAA[A/G]GGTCAACTAAGCAAA	161436
rs567281434	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670907	GAGCAAAACCTCTGA[A/G]AACTATGGGATTATG	161436
rs567290509	snp	C/G	0.000199203	0.00997807	intron-variant	EML5	GRCh38.p7	14:88634431	ACTATCATTACCAAA[C/G]AATATAAATAAAGCA	161436
rs567306364	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88643423	ACAATATTGTATAAC[A/C]AATATGTATACAGCA	161436
rs567306607	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88640450	TTGCTCCTGAATGAC[-/T]TTTGGGTAAACAATG	161436
rs567311732	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88693407	AATTGCTTATGCAGG[A/G]GAACTCCCATTTATA	161436
rs567327605	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770271	GGAGGTCTGATAAGT[C/T]ATTTTAATGAGGTTC	161436
rs567332377	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88791293	GCAACATACATGAGG[A/G]AATAACATTTTGTAA	161436
rs567352947	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709171	ATAATAAATATATGA[A/C]AATATCTTTCTGACC	161436
rs567367120	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88642702	TTCTGCTGTATTATA[C/G]TCTCTTAAAACTGAA	161436
rs567388201	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88645299	CCAAAGTGCTGGGAT[C/T]AGAGGAGTGAGCCAC	161436
rs567398244	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754519	TCACATACCTGTCCA[C/T]CTAAGTCAAACGCCA	161436
rs567399766	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730726	CATGAAACAACTAGA[A/G]ACAAGAATATATTCA	161436
rs567426582	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88673023	AAAAAGGGACTCCTC[A/C]CTAACTCATTTTTTG	161436
rs567449055	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773266	CTGTGAGTGAGCATT[C/T]TTCTGGACTGATAAT	161436
rs567471172	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88635304	CATGAGGAAAAACAG[A/G]ATAAAGTACTTAACT	161436
rs567486242	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88672613	AATGAATCCAGGGGC[C/T]GGTTTTTGAAAAAAA	161436
rs567488352	in-del	-/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88775311	TCACCAAGTGGGATC[-/T]TTGGGTCCCCAATTC	161436
rs567488423	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681253	ACATAGAGACAGACA[G/T]AAAACATGAAATGAA	161436
rs567514479	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700123	CTCAACAAGTATTTG[C/T]TGAATTAAACAAAAT	161436
rs567529728	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774879	GTATGTTCAACAGCC[C/T]AATTTAAAACCCCAC	161436
rs567553439	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707759	TTTTTATGTAGCTTA[A/G]TATAAGTCACTAATT	161436
rs567553599	snp	C/T			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614591	GGGTCAATACAGCAT[C/T]TTAAACCTCACACTT	161436
rs567572113	snp	C/T	1.68077e-05	0.00289889	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715064	CCAACTTTTTTATAA[C/T]GCTGAGCAACTCCAT	161436
rs567595850	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680738	CATCCAGAGTAAACA[C/T]GGGTTATATTGTTTT	161436
rs567599102	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775734	CGGCTTTACCACCTG[A/G]GTGTAGAACCCCAGG	161436
rs567611904	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793715	GTTTTCTTAAGTGAC[C/T]GCAAAGCTGAAGGTA	161436
rs567612320	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88684948	TCACTGTCAACTTTT[A/G]GCTCTTATATATTGA	161436
rs567615391	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705673	AATGATTAAGAGCTA[C/T]GTCAGTTGACATGGA	161436
rs567651547	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699450	AGTCTGACTCTCCAA[C/G]CTCCCCTTTTTATCT	161436
rs567661905	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671699	TCAAAATAAAGGGAT[A/G]GAGGAAAATTTACCA	161436
rs567672316	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667835	TTAGCTGCAATTTGC[A/G]GACTTCAGGAAGATT	161436
rs567715395	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624040	ATCCTGTATTGAAAT[G/T]TACTTCTTAGTCAAC	161436
rs567728375	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774262	TTTCCAGGTGATGCC[A/G]TTGCTAGTCTGAAGA	161436
rs567737116	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675239	CCCTTTTGCACTGCC[C/T]TAGCAGAGGTTCTTC	161436
rs567748787	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729678	GATTCTCGTGCCTCA[C/T]CCTCCTGAGTAGCTG	161436
rs567769043	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88632128	CCCATCCCATTTGGC[A/T]CACTGTTCAAGCAAA	161436
rs567784389	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88729281	CTGTCTTTTTTCTGA[C/T]TTCAAAGGAAAATCT	161436
rs567827005	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753693	ATTGACTAGAAGTAG[A/G]TGATAATTTAGAAAC	161436
rs567833094	snp	A/G	0.00134665	0.0259135	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715187	ATATGTACAACTTCC[A/G]TCATATCTCTGTTAA	161436
rs567843965	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88674172	TACTCAGGAGGCTGA[A/G]GCAGGAGAATCACTT	161436
rs567865512	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88762237	AGACACGGGCCATGC[A/G]TAGTGGCTCACACCT	161436
rs567908772	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88667379	AAAGAATATAAGACC[A/G]TGACTAAATTTGAGA	161436
rs567911288	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88697538	CTACTGCAGCACTCT[C/G]TCACTTATTTTTTAA	161436
rs567928421	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88617761	TGAGCCACTATATGC[C/G]TGGCTGATACAGGAA	161436
rs567946616	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655956	GGTGATCATTAAAAA[A/G]TCAGGAAACAACAGA	161436
rs567951833	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88629206	TATATTTGCCAAATC[A/G]TGATGAGGTAGACAA	161436
rs567956423	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714476	TCTAATATACAGCTT[A/G]TTGAGTACAGTTAAT	161436
rs567971957	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772179	TCCTCACTCATCTCA[C/T]GCATTCTATTAGCCT	161436
rs567988694	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703823	AAGAAGAAGTCACAA[C/T]ATCATTCCAAATTAG	161436
rs568008667	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718767	GTGATGTAAGAGAGA[G/T]AGACTTTGGTTTGAG	161436
rs568019902	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88772514	TGTAACAGCACTTTG[A/G]GAGGCTGAGGCAGGC	161436
rs568033469	in-del	-/TTT	0.00640164	0.0562125	intron-variant	EML5	GRCh38.p7	14:88769967	CAGCATTATGTGCAG[-/TTT]TTTTTTTTTTTTGGT	161436
rs568055349	snp	C/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88668323	GTCCTAAATGCAGAG[C/T]GCAGGAAGAAGAGAT	161436
rs568057403	snp	A/C			upstream-variant-2KB	EML5	GRCh38.p7	14:88794520	TACCCTGGGCAAAAG[A/C]ACACACAGTTTCTCT	161436
rs568081940	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756369	TCAAACTGACAAAGG[A/G]CATCTACATAAACCC	161436
rs568087660	snp	C/T	0.00874735	0.0655527	intron-variant	EML5	GRCh38.p7	14:88651160	TGTCATTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	161436
rs568101390	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622049	CCTCCCCCTTGTCCG[A/C]CTCCAGTAACCACTA	161436
rs568104772	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88697491	GAGGGGGTTAAAGTA[C/T]CAAGCATGTCTATAG	161436
rs568113437	snp	G/T	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621282	ATTTCAGCATTCCTT[G/T]TCCCAACAAGGATCT	161436
rs568120738	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767241	TTTGCAGTGCTACCA[C/T]ATGTACACACACCAA	161436
rs568143120	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88743087	ATTATAAAACAAAAC[C/T]CAGAGCTTTCATAAG	161436
rs568169758	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638017	TCGCATGAAAAATAA[A/G]GATATTAAAAGTATA	161436
rs568177858	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88682858	ACTGTCCCCTCTCCC[C/T]TTACCAAGTACTCAG	161436
rs568182574	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732757	AGTGGTTAAGTTTTG[G/T]TGTGATTTTCTGATC	161436
rs568211937	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88653373	ATCCTTGTCTTGTGC[C/T]GGTTTTCAAAGGGAA	161436
rs568257784	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763783	GGATGTTTAATTAGA[A/G]GTGACAAGAATAGAC	161436
rs568262869	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88640513	AAGTAGATTAAAACA[A/G]AGACACAACATACCA	161436
rs568269683	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88694934	AAAAAATACATGCTC[A/G]CTGTAGAAAACTTAG	161436
rs568299563	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88786297	ACATATATACATGCA[C/T]ATATAAAAATTTACA	161436
rs568301478	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88777617	ATGAACCAATAAAAA[C/T]AATAACTACAACAAC	161436
rs568305949	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88660144	TTACATTAGCCAGGC[A/G]TGGTGGCATGTGCCT	161436
rs568319472	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88712041	GAAAAGAAAGAGATA[C/T]AGTGCATTCATAACA	161436
rs568356352	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88758552	AGGATGTGGAAAAAG[C/T]GTAACCCTTAAACAT	161436
rs568369511	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88719564	TGCCTCTGAGGAGTT[G/T]GCTGTTGATAACACA	161436
rs568376164	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765904	CCCGAACGGAGGGAC[C/T]GGCTGAAGCCATGGC	161436
rs568396797	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88757743	TCAGCAGGGAAATAC[A/C]AATCAAAAATCACAA	161436
rs568412615	snp	A/G	3.31917e-05	0.00407367	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658212	TTCAGAATCAATGTC[A/G]GATTCTTCACTATCA	161436
rs568426060	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644382	TTGGGTGTTTTATAA[A/G]AAAGAACTCTGGATA	161436
rs568430865	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709719	CTAGTTATTTCACTC[A/C]TTTGAGAAACCTGCA	161436
rs568445294	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88658638	CTTTAAAAAACCAAC[C/T]TGGTATTCTGCATTA	161436
rs568460139	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702671	ATAATTAATTTTGGC[C/T]TTTTATCTGATCAAT	161436
rs568469150	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88743161	AGATTTGTTAAAGGA[C/T]ACAAAATTGTAACTA	161436
rs568471310	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752268	TTTAAAGCTAAGAAG[A/C]AAATATCTATATTTA	161436
rs568499255	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701725	GTGTTTAAAGCCAGA[A/C]AGACTGAAGGCTTTA	161436
rs568506043	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88735275	ATGCTGATGTTGCTC[A/G]TCTAGGAACCACACT	161436
rs568597498	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637282	AATCTAAAATTTACC[C/T]CTGTACTCCCCAGAT	161436
rs568598831	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740254	CTTGAAAACAAATAG[A/G]TAATTCAGTTAGAAA	161436
rs568608450	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751734	CTCCTGAAGAACACT[C/G]ATATTTAAGAAGCAG	161436
rs568619409	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88794442	GAGGAATAGCTTTCT[A/G]GCAGCTGCTGCAAAT	161436
rs568622637	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689710	GTACGCTCCAGCCTG[C/T]GTGACAGAGCAAAAC	161436
rs568655852	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88739454	CTATATATAACCAAG[A/G]TGGTATTTAATTATA	161436
rs568659701	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88705107	TCTTAAATGAAAAGT[A/T]AATTCATGAAATTTA	161436
rs568665650	in-del	-/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88704630	GTCCCAACAATGTCC[-/T]TTTATAATCATCTTA	161436
rs568690736	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747273	AAAAATTAGCCAGGC[A/G]TGGTGACTCACGCCT	161436
rs568694239	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88774402	AATACATAATAGTTA[C/T]ACATTGGAACGAATC	161436
rs568694268	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782833	ATCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG	161436
rs568723677	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655684	CATCATCAGAGTGAA[C/T]AGGCAACCTACAGAA	161436
rs568796325	snp	A/G	0.000117894	0.0076768	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706389	TCTGACATTAGTTAC[A/G]TGAGCTGAATGGCCA	161436
rs568829311	snp	C/G	0.00013138	0.00810388	intron-variant	EML5	GRCh38.p7	14:88744006	GTGACTATTATAAAA[C/G]AAGACCCTTCTAGTA	161436
rs568853421	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761347	CTAATGCTATCCCTC[C/T]CCTTGCACCCCAGCC	161436
rs568868058	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699306	GGCAAAAAAATAGTT[C/T]ACAAAGAGGCAAATA	161436
rs568907352	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88705714	AAAACAATCAAATGA[A/T]ATTACCTATTCAAGT	161436
rs568908158	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88698697	GGTATCTCACTTCTA[C/T]AGTTTCAGTGGTTAA	161436
rs568942937	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88755480	TCACCCATAATTCGC[-/A]AAAAAAAAATCTATG	161436
rs568943879	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713919	AACGGCTCACTGCAG[C/T]CTTATCCTCCCAAGC	161436
rs568968183	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88760724	GATTAGAATTGTATT[A/G]TATCTATAAAAAACT	161436
rs568976534	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662702	CACATGCCACCATGC[C/T]CAGCTAATTTTTTGT	161436
rs568978826	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88791101	CTTTTCTTATCTTTA[C/T]TCCATCTTGCCCTAC	161436
rs569023587	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678790	ATAATTCTTATTCTA[C/G]CTTGAAGACTTTTTG	161436
rs569035763	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685746	TGGGCCACCACAGCC[A/G]GCCCCCATGTGCTTT	161436
rs569060245	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633207	AATACTTTGTTTTAT[C/T]GCCATCATCTCATTT	161436
rs569060625	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648562	GTGCCTCATCAGATT[A/G]GCTAGGCTGATCTTT	161436
rs569074709	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88729720	ATGTGCCACCATTCC[C/T]CGGCTTATTTTTGTA	161436
rs569083906	snp	A/G	8.30737e-05	0.00644437	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616171	TCCAGCACTAACAAC[A/G]TGTCGATCACCACTG	161436
rs569092838	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88790363	AATTCGAGTATGTTT[C/G]TTGTTTTGTATAAGT	161436
rs569133515	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692417	TGTACTGAATACATA[C/T]AGACTTTTTTTCCTT	161436
rs569135264	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687837	AACACAATACTTTGA[C/T]GGCTGAGGTGGGAGA	161436
rs569147000	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615593	TCAAGTATTCGATCC[A/T]TCCTTGAAATGGCAT	161436
rs569158473	in-del	-/G	0.00119737	0.0244387	upstream-variant-2KB	EML5	GRCh38.p7	14:88793998	CCTCTAAAAATAATT[-/G]GAAATCCACAATTTA	161436
rs569191737	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88720558	TAGGTGCAGAAAACG[C/G]CTTTGATAAAATTCA	161436
rs569214022	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690421	CAGACCAAAGTGATA[C/T]CATAGAAGATGACGA	161436
rs569226087	snp	A/C	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684239	TGGAAGTTAAAAACT[A/C]GGCTCACTGCAAGCT	161436
rs569257674	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788221	AAATGTTATTCTGAA[C/T]CGCTTTTCCAATTAC	161436
rs569274772	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655118	ACTTTCCTCACAGAA[C/T]TGAACTACTGTAAAT	161436
rs569274821	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690292	GACAAGATCTGGCAA[C/T]TGATTTATTAAGAGG	161436
rs569276943	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704753	AATGTTGTATCCTTT[C/T]GGATATGTCATTTCA	161436
rs569311055	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88639870	ACGGGCATGAGCCAC[C/T]GTGCCCAGCAGGAAT	161436
rs569315582	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88698627	ACTTAAATACAAACC[C/T]CTCCCAAGGTGGTCT	161436
rs569328938	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88741913	CATTATCTATTCAAA[G/T]ATCTAATGAGTACTT	161436
rs569331608	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787424	AATTCATTATTCCAC[A/G]TTTTCCTTAATGTAT	161436
rs569366525	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88677772	CACCAGTCAGAATGG[C/T]GATTATTAAACAGTC	161436
rs569374267	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687773	AAAAAAACAAAAAAA[A/C]CACAAAACAACAACA	161436
rs569375135	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88645968	AACCTTTAATTTTTT[A/T]AAAAAATGCAATTTA	161436
rs569390288	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623855	ACAAGTGTTGGAGGA[C/T]GAAATAGAGCCCATT	161436
rs569404818	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88750342	TTTAAAGGAGTTAGA[A/G]TGCCTGATATATGGT	161436
rs569478296	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88789755	AACCAGTAAGCAAAT[A/G]ATAGACTAGTCATGA	161436
rs569480060	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88773744	TAACTTTCTATTAAG[C/T]AGCCAGGGTTGAGAA	161436
rs569490131	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669173	TCTGTGCAACTGGTG[A/G]ATCAGGAGATCCCCT	161436
rs569538263	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681355	GTGGCTCACGCCTGT[A/G]ATCCCACCACTTTGG	161436
rs569543341	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88717803	AAACAAATTAAAGGA[G/T]CATAGTAATAGGATC	161436
rs569558105	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631073	ACTACCAGAGAGTGA[A/G]TTTTCTCTGCTTAAT	161436
rs569570989	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784492	TTCAAAGGATCATTA[A/G]TGGCTTCTATGACCA	161436
rs569580041	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725908	AGAGAGAACTGTGTT[A/C]ATAGTTTCTGAATTG	161436
rs569583282	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88633910	CTACCATGCTTGTCC[-/A]AAAAAAAACCATTAC	161436
rs569591253	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88731269	GTCCCCCTTCCTGTG[A/T]CCAAGTGTTCTCATT	161436
rs569607384	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB	EML5	GRCh38.p7	14:88793392	AAATTATTATTTTTA[A/G]AAACAGAGCCTCGCT	161436
rs569630044	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738322	AGGTCACACAACTTG[C/T]AGGTGACTGGAATAT	161436
rs569635111	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88680800	GGATTCCCACACCCT[C/T]AATCCAGACATCATG	161436
rs569656603	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638518	TGCTATTGACTTAAA[C/T]CTTTTTGCTGACCAG	161436
rs569658210	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88704754	ATGTTGTATCCTTTC[A/G]GATATGTCATTTCAG	161436
rs569666235	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671009	CATCCAGGAGAACTT[C/T]CCCAACCTAACAAGA	161436
rs569668001	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626516	GTAGTCCCAGCTACT[A/G]AGGAGGCTGAGGATC	161436
rs569668808	snp	C/G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88668937	TCCCACCAAGAAGAC[C/G/T]GAAAACGGCAAGTGA	161436
rs569692173	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783831	ATAGATATTTGCAGA[A/C]TATTTCATCCAATGG	161436
rs569696754	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636224	GTAGGTTCAGGACCA[A/T]CTGGTAGAGAATTCT	161436
rs569696880	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674294	AACAACAACAACAAT[A/G]AAAACCCTGAGACTT	161436
rs569698763	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636614	TGCAGTGAGCCGAGA[C/T]TGTGCCACTGCACTA	161436
rs569728288	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88671812	GACAAAGATGGGCAT[G/T]GTATAATGGAAATGG	161436
rs569739640	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88710250	TGAAATTAAAGTGCA[A/G]TATGTAGGGTATATG	161436
rs569740239	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88709893	ACTGAATCAGTCCCC[A/G]TTATAAATTTTTCTT	161436
rs569757851	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88644068	CGCACAGGGTCAAAA[C/T]TCCTATTTGGTATAA	161436
rs569760410	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770536	TGAAACAGGGAAAAA[A/G]GAGTGGGATCCAGTA	161436
rs569788341	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88746566	AAAAACTAAAAATAC[C/T]AGATAAAATGTAAAA	161436
rs569811331	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619916	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	161436
rs569817265	snp	A/G	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88666975	GCAGCAGTGGAGGTG[A/G]TAAGAGGAAGGATTT	161436
rs569819097	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88658816	AGTTAATTACAATGT[A/G]TATGGAATAGTGTAT	161436
rs569859043	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88775055	AGGACCTACTCCTGG[C/T]AGCATTCACCACCTG	161436
rs569859557	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709808	GAATTGCAGCATATA[C/G]TTACAACACAATATT	161436
rs569874477	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88627137	ATACATAGTTCAAAA[A/G]ACAAAGGCTTAGAAG	161436
rs569876465	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673104	AGAAAACTCCAGGCC[A/C]ATATGACTGAAGAAT	161436
rs569876938	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770934	TATTAATATTGCTGA[A/G]TAATGGAAATTAATT	161436
rs569882025	snp	G/T	0.000119616	0.00773263	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88620816	TTTTAGAGAACTCAC[G/T]AGTAAAATGATAAAT	161436
rs569914028	snp	A/C	0.000293937	0.0121195	intron-variant	EML5	GRCh38.p7	14:88682052	AAGAAAACATAGGAT[A/C]AATTTAGTGTATGTG	161436
rs569914200	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88694023	AGTGATCCTCCCACC[C/T]TGGCCTCCCAAAGTG	161436
rs569920604	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88769423	GCTATGCTTCCTATA[A/C]AACCTACAGAACTGT	161436
rs569953968	in-del	-/A/AA			intron-variant	EML5	GRCh38.p7	14:88620935	CATCTTCTGCATTTA[-/A/AA]AAAAAAAAAAAAAAA	161436
rs569986945	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88648410	CCAAGCTAGAGTGCA[A/G]TGGTGTGATCATGGC	161436
rs570007503	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88762279	ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACCT	161436
rs570012906	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88770339	TGTTCTATTTCCTAT[A/G]CTTTTTCTAGAAATT	161436
rs570017446	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88744312	GAACTTCAAACACTA[C/T]TGGAGTAAAATTTAA	161436
rs570028166	in-del	-/AAC			intron-variant	EML5	GRCh38.p7	14:88726156	CATAAGGCTGTAAAT[-/AAC]AACAACAACAACAAC	161436
rs570092759	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715491	ATAAAGGAAATAAAG[G/T]AATAGATTTTTATGG	161436
rs570126339	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617416	CCTCCCAAAGTGCTG[A/G]GATTACAGGCTGAGC	161436
rs570127585	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88724210	AACCTGGGAGGCGGA[C/G]GCTGCAGTGAGCCGA	161436
rs570156368	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88624811	GACCAGAAATGAGAA[C/T]CAAATAGAAGGCACA	161436
rs570165370	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88691504	ATGTTCCTGTTACAT[A/G]AGGTCATATAATCAG	161436
rs570168121	snp	C/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88722329	TGTATGTTCACTGCA[C/G]CACTATTCACAATAA	161436
rs570173053	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88787269	TTAGTGCTATTCCTA[A/G]TATACATATGCTCAT	161436
rs570186455	in-del	-/ACTCTG	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88690954	CTAGAGCAGGTTAGC[-/ACTCTG]AGCTGCAGAGACCAA	161436
rs570189635	snp	A/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88700785	CGGAAAGGTTAGATC[A/G]TAAACCATTAAATAC	161436
rs570207645	in-del	-/TTGT	0.00369912	0.0428472	intron-variant	EML5	GRCh38.p7	14:88760344	TAATGTAGGTTATAG[-/TTGT]TTGTTTGTTTGTTTT	161436
rs570225981	snp	C/T	0.000102854	0.00717053	missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792418	TTGGCCGCAGTGTAG[C/T]AGAGGTTGTTGCGGC	161436
rs570228579	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657707	ATTACTAAGTAATAA[C/T]AGCAGGTTAAAAAAT	161436
rs570259626	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772613	AAAAAATTAGCAAGG[C/T]GTGGTGGTGCGTGCC	161436
rs570290551	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690999	CTTCTCTGCACCCAG[A/G]GTCTGCCTCCCTGGT	161436
rs570303518	snp	G/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88694582	TAATATGGTAACTCT[G/T]CTCAAGAGAATCTCA	161436
rs570309315	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649443	TTTCACATCACCAAA[A/G]GTAGATATAAAAGTA	161436
rs570343868	in-del	-/ATC	0.00438332	0.0466095	intron-variant	EML5	GRCh38.p7	14:88634552	TGTAAAAACCCAAAT[-/ATC]ATATTAATTATAATT	161436
rs570371051	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88657019	TTTTTTTGAGACAGG[A/G]CCTCATTCTGACACT	161436
rs570413027	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613915	ATACAGCGAGGTGGT[A/C]AGCTGATGACTACTT	161436
rs570466004	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88739550	ACTTAAAAAATAACT[A/G]TTTATAACTAAATAT	161436
rs570475894	snp	C/T	0.00517822	0.0506191	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622125	AGGAGTGAGAACATG[C/T]ATTTATCTTTCTGTG	161436
rs570487032	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622833	AAAGGCCCTGATATT[G/T]ATAATTTACCTCTAA	161436
rs570531707	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727253	ATAATAATGTCACCA[C/T]ATGGTAATGCACATA	161436
rs570544463	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88788226	TTATTCTGAATCGCT[G/T]TTCCAATTACAATTT	161436
rs570550969	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781103	CTTAGCTGTGATGTA[A/T]ACTCACAATTTAGGC	161436
rs570553792	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88675980	CTCCATCTGAGACCA[C/T]CTCAGCCTGGATTTC	161436
rs570567415	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718831	TTCTAATAGGGCTCT[C/T]TGGTGGGGGTGCAAC	161436
rs570581107	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88662897	GTATTCTGACTCAAT[A/C]AACTCAATAATATCC	161436
rs570591795	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646542	ATTCTATGTTACTGT[A/C]TGACAGCTTTAAATG	161436
rs570611806	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88742032	TGAATCCATTATTTT[C/T]TTCTAGATCAGTGAT	161436
rs570622732	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625453	GTTGCCCAGGCTGGA[A/G]TGCAATGGTGCGATC	161436
rs570690037	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667056	GGTGAAAGGCGTCAA[A/G]GGCATGGTTTTGCTT	161436
rs570724084	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88750493	TACTACTTAAAGGAG[C/T]TAGAGTGCCTGGTAT	161436
rs570725115	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88644987	AGAGTGCTGGGATTA[C/T]GGGATCAGGAGTGAG	161436
rs570772023	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633317	TGTAGAGACAGGGTC[C/T]TGCTGTTGCCCAGGC	161436
rs570793609	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88652525	TCTGAGTTCCAAAAT[C/T]CTTCAGCACTATCCT	161436
rs570809162	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88702879	CCCACCTCAGCCCTC[C/G]AAGTAGCTGGGACTA	161436
rs570815347	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88637425	GACCATGACATTTCT[A/T]AACTAAGAAAGAAAA	161436
rs570835010	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689224	CAAGTGCAAGAGTTT[A/C]TCTAGGAATGCCTGG	161436
rs570837466	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651932	TTGAAATATACCATA[A/G]GTTAGGGATTATAAT	161436
rs570861497	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88736189	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT	161436
rs570871333	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695678	TCGCACCTGATCTCC[G/T]TTTCCCTTATCTATC	161436
rs570871884	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88745027	CAAAAACTCCATTGA[C/G]AGTGTCATATTTTGT	161436
rs570889876	in-del	-/A	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88658506	CAAGTGCAATGTGTT[-/A]AAAAAAATGAGAAAA	161436
rs570943797	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88731882	CTTTTGAGAAGTGTC[C/T]GTTCATATCCTTTTC	161436
rs570945863	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675307	CATCCAGGCATTTCC[A/T]TACATCCTCTGAAAT	161436
rs570980851	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682938	TCAACTCCAGAGCCC[A/T]GGTTCAGAGATTCTG	161436
rs570996025	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88659243	GAATGACGACTCTCT[C/T]TTTTTTTTTTGATAC	161436
rs571006745	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88758021	CACACCTGTCTAATT[-/T]TTTTTTTTTTTTTTT	161436
rs571046408	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88787289	CATATGCTCATTGAG[C/T]ATCTGATTGTGTCTA	161436
rs571048615	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88735072	AGAAATATTTACAGA[A/T]GAAATCAGGGAAAAA	161436
rs571067524	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733681	ATCTCCCATCCCCCA[A/G]AAATAGACTGGCACA	161436
rs571122419	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649243	GTCTCATCATGTTGT[C/G]TAGGCTGGTCTTGAA	161436
rs571139087	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88635247	AAATAATGATTTAAA[A/G]AACATATTGATAACA	161436
rs571141094	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625684	TGGGATTATAGGTGT[A/G]AGCCACTGTGCCCGG	161436
rs571170526	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700023	GTCCAATTCTTATAC[C/T]ACATTGTGAGCTCCC	161436
rs571196298	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768337	TTTCTCTCCTCAAAC[C/T]TTCACCCACTAATTT	161436
rs571199861	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88689716	TCCAGCCTGCGTGAC[A/C]GAGCAAAACCCTGTC	161436
rs571200422	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88634199	TGTAGTACCTCCCCT[C/T]TCTCTCTCTTCCTCC	161436
rs571253443	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88753288	GCTACACCCTTGTTA[C/G]AAGTCCTGCAAAGGG	161436
rs571260213	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88685850	TTTATATTATTTTTA[G/T]TGTTCTATTGTTACT	161436
rs571272854	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699374	GTTAAATGCCTTGAA[C/T]TGCATTGGGAGTCAA	161436
rs571292861	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88790602	AATACAAGTGTACCA[C/T]GAGAAGACCTCAAAA	161436
rs571299152	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648706	CCTCCCTTCCTCCTG[G/T]GCTTTCTTCTAGCCC	161436
rs571301400	in-del	-/CAA	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88673729	AGCATTCCTATATAC[-/CAA]CAACAGAAAACAGAG	161436
rs571331152	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684818	AACAGAAAAAAACAA[A/T]TTTTTTCTGTATACA	161436
rs571334183	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775674	TCTGGACCCACCCAA[A/G]CCTGGGGGAACTCAC	161436
rs571340301	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88779010	AGATTGTAGATTGTA[C/T]ATGTGAGAATTTTTG	161436
rs571343972	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88656618	ACTTAAAGTATAATT[A/T]AAAAAAAGTGATCTC	161436
rs571371457	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783445	ACTTCACCTATAAAT[A/G]CACACACGGACTGAA	161436
rs571374894	snp	C/T	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88655745	GACAAAGGGCTAATA[C/T]CCAGAATCTACAAAG	161436
rs571390003	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730820	CTAACTGATGGTGGG[A/G]AAAAAGTATGTATAG	161436
rs571404717	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88680906	AGGAGGGAGTCAGCA[A/G]AAAAAAAACAAAAAC	161436
rs571417903	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703642	TCTTGATAAGTATTA[C/T]CAGTCAGGTAAGAAA	161436
rs571442713	snp	C/T	0.0475351	0.146656	intron-variant	EML5	GRCh38.p7	14:88684242	AAGTTAAAAACTCGG[C/T]TCACTGCAAGCTCCG	161436
rs571494646	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730230	GCTGTGCTAAAAGGA[A/T]ACAAATATACATTAC	161436
rs571520637	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88715776	GATTCTCACCTCATA[A/C]CTCAGCCTCCCGAGT	161436
rs571575668	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88677124	TGGCCAGACTGGTCT[C/T]GGACTCCTGAGCTCA	161436
rs571579870	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677870	AAATTAGCTCAACCA[C/T]TGTGGAAGACGGTGA	161436
rs571604987	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780214	TGCCTCAGCCTCCCA[A/G]AGTGCTGAGATTATA	161436
rs571641711	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88640376	ACCCACAGTGCAAAA[C/T]AGAAATCAATACCAA	161436
rs571642171	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88649344	ACAGGCCTGAGCCAC[C/T]GTGCCCAGCCATGAT	161436
rs571645588	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773860	ATAGTGGCTCATGCC[A/T]GTGATCCTAGCATTT	161436
rs571650874	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773710	GGCCATTGGTGGTTT[C/T]ATTTTGTTTGTTTTC	161436
rs571652706	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729146	CTTTCCAATCTGTGT[A/G]TGTGTACGTGTACAT	161436
rs571656261	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647315	GTTGCAGTGAGCCAA[G/T]ACTGCATGCGCCACT	161436
rs571657912	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88718470	AGGTAAGCTGAAAAC[-/AG]AAAGAGAAGAAACAC	161436
rs571664598	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88734848	AAACTGTAAGAAGAA[A/C]AAAAAGGGAAGGAAG	161436
rs571692644	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687522	CAATATTTACAGTGA[C/T]CCTAAACATTTTACT	161436
rs571696724	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631868	TAATGTATTTATTCT[C/T]CCACATTGCAAAGTG	161436
rs571747299	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88735349	TATAAACAGGTATCA[C/T]TAGATCTTATTTAAA	161436
rs571748696	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760796	CCATAAACATAGTAC[A/G]CCCGCCCTCCATTTT	161436
rs571748803	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88706500	AACAATTTTTATATA[G/T]GAACCACTGTATCAT	161436
rs571761415	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631232	TTCTTTTTTCTTTTT[C/G]AGACAAGGTCTCACT	161436
rs571773516	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639961	ACCTTGTAAGGCTAT[A/G]ACAGTAGTCCATGCA	161436
rs571776711	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761567	TTCCATGGTGTGTAT[A/G]TGCCACATTTTCTTT	161436
rs571793693	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88617273	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATCAC	161436
rs571813323	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88783494	GATATTCCATGCCAA[C/T]AGAAACCAAAAAAGA	161436
rs571834319	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88670669	AGAAGCTAAGAGCCA[C/T]GATAAAACATTACAG	161436
rs571841381	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663497	ATGAAACAATAACAT[C/T]CTTAAAAAGAGAGGA	161436
rs571871849	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767563	TCATAATATTGTTAC[A/G]CTGTAAGAGTTCTTA	161436
rs571873112	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763920	AGTGGACTTCTAGTC[C/T]TAGTTTGCTAAGCAT	161436
rs571884736	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88664199	GGAGGATGACTTAAG[C/T]CCAGGAGGTTAAGGT	161436
rs571895446	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678618	TCCAAAATACTCATA[A/G]TGATTAATACCATTA	161436
rs571929461	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623968	TGTGCATTCTTCCTT[C/T]ATGTAAAAGGCACAA	161436
rs571986769	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88611951	AACATTGGGTGTTTT[C/T]GTTTTGTTTTTACTA	161436
rs572001071	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664588	TATATATCTATAAAG[C/T]TGTCATGGGATGCTA	161436
rs572001756	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619260	ATCCCATCTACTCGG[A/G]AGGCTGAAGCAGGAG	161436
rs572018736	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709842	CAGCAGTGAAAAAAA[C/G]GCATTAAAGCTACAC	161436
rs572027772	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88673190	AAGATTATCCACCAC[A/G]ATCAAGCTGTCTTCA	161436
rs572032174	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88716639	TTTTGGTATTTTTTA[C/T]AGCATTTTTGTTTAG	161436
rs572051073	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88763896	ATGCTTTTATAGCCG[A/G]GTTAAAGAAGTGGAC	161436
rs572076961	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672694	GACACAATAAAAAAT[A/G]ATAAAGGGGACATCA	161436
rs572082997	in-del	-/TGG			intron-variant, cds-indel	EML5	GRCh38.p7	14:88792159	TTGTAGGGTGTTAAC[-/TGG]TGGACTCGGGACCAG	161436
rs572093406	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88725361	TTAAAAACCGGTCTC[A/G]GAAAGGGGAGTCAGC	161436
rs572114806	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88620020	CTAGCAATCTTTGGA[A/G]TCATATGGGACAATT	161436
rs572120258	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88701668	GGAGGATGCAAGTTG[A/T]TCCCTTTTCCACATA	161436
rs572121587	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88644643	TCTGTGGTCCACTAG[A/G]CTGCCCTCTTCATCT	161436
rs572126604	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769957	AACTAGATTACAGCA[A/T]TATGTGCAGTTTTTT	161436
rs572179076	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88695238	TTTATTCAATGGTAA[C/T]AAACATGGAAGCAAT	161436
rs572189687	snp	A/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657253	TTTCTAAGAGGTGCT[A/G/T]TGAATTGTCTATAGC	161436
rs572198667	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88695844	AAGAACTTTGAGTAA[C/T]TATGAAAAGTTAATC	161436
rs572206988	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765964	GACATTTATTAGCTC[C/T]CCAAATTAATACTTT	161436
rs572268190	snp	C/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88785186	GGTTACCAGAAGCTG[C/G]AAAGGGTCGTGGAGG	161436
rs572291437	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755873	ACATAGCAGCATACA[C/G]CTCTATTCCCAGCTA	161436
rs572313171	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679882	GTATAGAATAGTGTA[C/T]AGTATAGTGTAGCGT	161436
rs572313993	snp	C/T	0.00716266	0.059414	intron-variant	EML5	GRCh38.p7	14:88745255	TCCAAAATGCGAATA[C/T]ACACAAAATTTTCTA	161436
rs572319781	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649670	AACTATTCATTTGCA[C/T]TGTAGTAGTTTGTAC	161436
rs572341969	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88693478	ACAGTATGGCGAACC[A/G]CCCCCATGATTCAAT	161436
rs572356956	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651377	CAAAGATTTCAGTTA[C/T]GACAGTGTTAATCAT	161436
rs572369504	snp	C/G	0.0143877	0.0835874	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792545	CTCGGGCCCGCGGCG[C/G]CGACGGGAGGCGGCG	161436
rs572374780	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686855	GGAAAAAAGGCCTGT[A/G]AGGCTACAGAAACAG	161436
rs572401013	in-del	-/TATT	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88676894	GGGGAGAGGATTTCC[-/TATT]TATTTATTTGTTTGT	161436
rs572413126	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88658912	ACACATGCCTATGTA[C/T]AGCATGAGTATGTTA	161436
rs572419206	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88650790	CCTGGTACAGGCATG[G/T]ACTACCATTCTTGGC	161436
rs572471505	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88699680	ATGGAAAAATTAAAG[A/G]TGAAAAGAATATTGA	161436
rs572536188	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88775934	GAGAGACTCCATTTG[C/T]TTGGGAGAAAGTAAG	161436
rs572542511	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88752928	TCGCCATACCACTTA[C/G]AGCCACTTCCATTGC	161436
rs572577181	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783926	TCATAAGACAAGTCT[C/T]AAAATGTTGAAAAAC	161436
rs572583093	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88637935	AAGGAAAAACACAAG[A/G]GTCTATGTGGCATAG	161436
rs572588587	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88645566	TGAACGTTCCACACT[C/G]TTAGCAACATAAATC	161436
rs572588983	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653566	AATCATGTGGTTTTT[A/G]TCATTGGTTCTGTTC	161436
rs572596135	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672277	TACACAGAAATTGAA[C/T]AACCTGCTCCTAAAT	161436
rs572612915	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88728974	TTTTAAAATTGTTAC[A/T]AGTTTATAGGAAAAA	161436
rs572627170	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88775338	ATTCCAGAACCTGAC[A/T]CTTAGATGGCATTTC	161436
rs572628484	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88687116	GATGCCCAACAAGAC[A/G]GAAAAATACATGCCA	161436
rs572638925	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731002	TTCATTTGCTCCTGT[A/G]GATTTAACTAACCAC	161436
rs572642556	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88758759	CACAAATGGCCAAAA[A/T]GTAGAAACAATCCAA	161436
rs572652319	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88694088	AATGTTGACATCTTA[C/T]ATTACCATAGACCAT	161436
rs572655053	in-del	-/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88744550	CTGATTTTACAGTAA[-/T]TTTTTTCACTGTTTA	161436
rs572692637	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88643728	AGAACTCAAACAGTA[C/T]ATTCATCATCGGTGG	161436
rs572707220	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676588	TTCAATGCTATTCCC[A/G]ATAAACTACCATTGA	161436
rs572707604	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88625888	TGCACTTAGTTTTTC[A/G]ATGCACCAAAGGATT	161436
rs572708847	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88711494	CATGAGATCACAGGA[A/G]AAACTACCATTTATA	161436
rs572742395	in-del	-/A	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88732576	TTCCATATGAACTTT[-/A]GTTTTTTCCACTTCT	161436
rs572767374	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717232	GGACCTGTTTCAGCA[A/G]AGACAACAGTATGTG	161436
rs572769073	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683988	AAAAAGAAATAGCAG[A/G]CATCCAGATTGGACA	161436
rs572772671	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88634742	CATAAACTTTTAATT[A/G]TAATAACTTTTAAAA	161436
rs572776465	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714164	TTTGAGATAAACACA[A/C]AAAAAATGTATTGGT	161436
rs572807044	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88686261	AAAGGCCCAGAAGTC[-/AG]AGAGAGTGTGGTGCT	161436
rs572811649	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737198	CTCACCAAGCAACAG[A/G]AGAGGGAGCCGCTGG	161436
rs572814439	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88684306	CTCCCAAGTAGCTGG[A/G]ACTACAGGCGCCCGC	161436
rs572851526	in-del	-/T/TT	0.480064	0.0978296	intron-variant	EML5	GRCh38.p7	14:88698265	GGTTCTCCAGTTTCC[-/T/TT]TTTTTTTTTTTTTTT	161436
rs572900761	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88768991	AACCATGCATTCCCA[C/T]TGGGAGCAATATCAT	161436
rs572934896	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88628776	TATACCATCTGCTAT[C/T]TGTAATACACAATGA	161436
rs572947743	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704780	TTCAGGGGATACAGT[C/T]AGTTCTATCATTAGA	161436
rs572978537	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88773393	CAGGGAATATCCAGC[A/G]TGGGAGGGCCTTAGG	161436
rs572980392	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88704159	CTGATCCCTCATGAA[C/T]GGCTTGGTGCCATCC	161436
rs573010502	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691050	TGCCCAGAGTCTGGG[C/G]TGGTCCCCACCTACA	161436
rs573014535	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779639	TGTTTGTCACCCTAC[C/T]AGTCTTTTATATATC	161436
rs573015997	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88780454	AGTCAGGGTTCTGCA[A/G]AGAAACAGAATAGAA	161436
rs573033080	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88728408	ACTACTAGTAGCCTA[C/T]TGTTGACTGGAAGTC	161436
rs573033896	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731758	TTTTTAATGATCACC[A/G]TTCTAACTGGTGTGA	161436
rs573082693	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766141	CTGAGGATGTATGTC[A/G]CCTCAGGACCCTGTG	161436
rs573082795	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88757978	CTGCTTTGGCCTCTC[A/C]AGTAGCTGAGACTAC	161436
rs573089804	snp	A/C	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88742210	ATTGTTCTAGAATCC[A/C]AATCAATATTGACCA	161436
rs573091317	snp	C/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88630687	CTTTGTGTCCTCACG[C/G/T]AAAGTCAGGCTAAAA	161436
rs573100873	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623140	CCTACCTCAGCCTCC[C/T]GAGTAGCTAGCATTA	161436
rs573111147	in-del	-/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88782503	GGCCATGTCAGAGAC[-/T]TTTGCGGCAGCCCCT	161436
rs573116584	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88726179	CAACAACAACAACCC[A/C]ATTTTAACAGCCTCA	161436
rs573117214	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765477	ACATTGAGTTCTTCT[C/G]AAGCTTTGAATCTTT	161436
rs573120684	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756414	ATTTAATGATGAAAG[C/T]CTGAAAGCAATCCCA	161436
rs573128830	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783943	AAATGTTGAAAAACA[C/T]TGAAATAATATCAAG	161436
rs573155846	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88764924	TTGTTTTATAATATA[C/T]AGCCTATTTTGGTAA	161436
rs573171189	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88734925	ATATATGAAGCTCAT[C/T]TGGGTCCTGATTTTA	161436
rs573180863	snp	C/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88778575	CACGAGGTCAGGAGA[C/T]CCAGGCCATCCTGGC	161436
rs573216794	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88621744	AATAAGTACAAACAC[A/G]CTCAAAAATTTTCAT	161436
rs573266489	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88636707	GATAAGACTCAGGGA[A/G]AATATGCTAGCTGTC	161436
rs573266588	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778709	ACTTAAACCAGGGAA[A/G]CGGAGGTTGCAGTGA	161436
rs573269275	snp	A/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88674582	AACACATGTGAATTC[A/G]AGATGAGATTTGGGT	161436
rs573275763	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756570	TGATATGATCATATA[C/T]ACAGAAAATCCTAAG	161436
rs573295244	snp	C/T	0.00597247	0.0543191	intron-variant	EML5	GRCh38.p7	14:88645027	CCAGCCTTTTCTCTT[C/T]TTTCTTTCTTTCTTT	161436
rs573339021	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88785860	ATAGGAGCCAGAGTG[A/T]CTTTGTTAAACCGTA	161436
rs573343455	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681801	TATTTAAAGCCTTTT[C/T]AAAATGTGCCTAGTT	161436
rs573398698	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729840	TACTGGGATTACAGG[A/C]ATAAGCCACCACACT	161436
rs573405858	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668054	TGGTGGCAGCCACAC[C/G]ATTTCCAAACAGGTC	161436
rs573415428	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88759188	GTGAAAAAAAATACT[G/T]ACATTACTGTCTGTA	161436
rs573424433	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	ZC3H14, EML5	GRCh38.p7	14:88614109	TAATTTCTCTGTAGC[C/T]AAAAGCTGGCAAACT	161436
rs573438518	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88772382	TCTGATCTCATCATT[C/T]ACCTCGGTAAAAACC	161436
rs573452343	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88724964	GTAGTCTTTCATCTC[C/T]CTTCAAGAAGCTGTT	161436
rs573469078	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88719041	AAGTTGATAAAATGT[G/T]GTAGTAACACTGTCA	161436
rs573483328	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718180	ATCATGAGTTCAGTT[C/T]TGGAAATGCTGAGTT	161436
rs573491581	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88667399	TAAATTTGAGAATAG[C/T]GTAGGTCTTCTCTCT	161436
rs573541900	snp	A/T	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88775183	TAGGATACAGCACAT[A/T]ATCAACTGTGGTGGC	161436
rs573545052	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88787385	AGAAAACTTTGAAAT[-/A]AAAAGTTCTTAATAG	161436
rs573552795	snp	C/G	1.81e-05	0.00300827	intron-variant	EML5	GRCh38.p7	14:88618377	TTCCATTAGGTGAGA[C/G]ACAAAATCCACAGGG	161436
rs573566077	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768093	TTTGGATTTGTCATG[A/G]TTTCTCATGATTAAA	161436
rs573604774	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774713	CCCTACATTAAAATG[C/T]TGGAGTGCCACAGGA	161436
rs573611203	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88675457	GGCCCCTTTTAGCTA[C/T]GGATGGAGCTGCTGG	161436
rs573617804	snp	A/G	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88723186	CAGCAGCTGAGGCAG[A/G]AGGATTGCTTGAGGC	161436
rs573622413	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88685895	AGCATATTTTCTATT[G/T]GCAGTTGGTTGAATC	161436
rs573650328	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88683033	CATTTACAGCAGAGT[A/G]TGAAAAAGCTCATGC	161436
rs573652899	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88633481	GTGTGATATTCAAAA[A/G]CTATTTTTGTTTTTT	161436
rs573666914	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641641	TTTCATGTTAAAAAC[C/T]TTCAACAAACTAGGA	161436
rs573672661	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88679564	AGCCGTGGTGGCGCA[C/T]GCCTGTAGTCCCTGT	161436
rs573682874	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678967	GTTGTGAAAGTTCTT[A/G]GGAATAATCCTTCCT	161436
rs573682982	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768403	CTACTAAAATATTTC[C/T]GTAATGTGATTGTCT	161436
rs573701338	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782938	TACAGAATTAGTCAG[A/G]TGTGGTGGCACACAC	161436
rs573724724	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641620	TTCGATAAAATCCAA[C/T]ATCCCTTTCATGTTA	161436
rs573739735	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782271	GTGGAACTTTGAACT[C/T]AAGAGAGATGATTTA	161436
rs573747020	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705443	GATAAAGAAGAAATT[A/T]GACTTTTTAGAGAAA	161436
rs573757296	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88693266	TTCATAAAGACATAC[A/C]CAGGACTGGGTAATC	161436
rs573794911	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706929	GACATTAAAAAGTCA[A/C]TCAATGTAATGCATC	161436
rs573807537	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710141	AAGAGTCCTGGATTC[C/T]TTCAGAGAGATTATG	161436
rs573840265	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715787	CATACCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	161436
rs573865151	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88735734	TTCACTGCAAGCCCT[G/T]TATTTCTAAAATACA	161436
rs573893816	in-del	-/CTG			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, cds-indel	ZC3H14	GRCh38.p7	14:88612253	TTAAAATATTCAATT[-/CTG]CTTTTTAATTTTTAA	161436
rs573907763	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88664075	TTGAGTCCAGGAGTT[C/T]GGGACCAGCCTGGGC	161436
rs573910386	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662944	GAGAACAGACTTCAC[A/G]TGTAACTAAACGATA	161436
rs573932534	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708220	TAATTTTTAATAACT[G/T]GTTCTGATAAATGGG	161436
rs573994573	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88714006	CCATGCCTGGCTAGT[G/T]TTTGTATTTTTAGTA	161436
rs574004601	snp	G/T	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88774034	TGAGGCAAGATAATC[G/T]CTCGAACCCGGAGGC	161436
rs574025718	in-del	-/TAGAGC	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88669227	CTTGAGTCCCAAGCA[-/TAGAGC]TGCACAGATTCTCAG	161436
rs574036703	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750095	ATAGCAAAGACCAAA[C/T]GGCCCACAAAGTTTA	161436
rs574037476	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721555	GTGCTGGGAAAACTG[G/T]CCAGCTATATGCGGA	161436
rs574049538	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725395	TGTAGAGGCTCAGAA[A/G]TACAAGAAAACATAA	161436
rs574063008	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760866	AGTATATAACATAGA[A/C]CTTGCATAGATTTTG	161436
rs574077925	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88657566	TTATGATCTTATAAA[C/T]TGGATACAAAGATGT	161436
rs574086844	snp	A/C	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88753771	TTTTGTATAAAAAAT[A/C]ACTCATAGGAATTGT	161436
rs574091343	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760436	TTTCTCCATTGACTT[C/T]CCCAAGCACTTTTGT	161436
rs574099874	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767255	ACATGTACACACACC[A/C]AAGGGGCAAATCTGA	161436
rs574114839	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660668	GAATAGCTTGAACCC[A/G]GGAGGTGGAGGTTGC	161436
rs574123874	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616412	GATCTGCAAAACCAG[C/G]CTGTGTGGGCAGTCA	161436
rs574134168	snp	A/G	0.000502418	0.0158416	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615832	CTCAGTGAGGTGTAT[A/G]TACACATTTCCAGAC	161436
rs574148644	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692685	GCTGCGAATTTGCAA[C/T]TACAAGTGACTAAGG	161436
rs574151430	snp	C/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88640625	AAGATCCCAAATTAA[C/G]AATCTAACATCACAC	161436
rs574197233	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88623585	TGCCTGGCTAATTTT[C/T]GTATTTTTAGTAGAG	161436
rs574224308	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88666501	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACAG	161436
rs574231934	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	EML5	GRCh38.p7	14:88766773	GCTTGAGGGGCATCA[C/T]GGAACCTGCCAACAT	161436
rs574258512	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648797	GATGTGAGGCTAGAT[C/T]CGGGTGCTTTATTTC	161436
rs574299635	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791909	CATCAGTCCTTTATT[A/G]GGTAAAGGGTTTCCC	161436
rs574319486	snp	C/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88789555	TAGTCATGATTCAGC[C/T]TTTACTGAGAAAATG	161436
rs574358697	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692134	AATCCCAGCACTTTG[C/G]GAGGCCAAGGCGGGT	161436
rs574372826	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647944	ACTGGAGATACTTCA[A/G]AGGAAATTGTCTAAA	161436
rs574381279	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88764707	AAAAATATGCATTTT[A/C]ATGCTCCAAATTTCC	161436
rs574402183	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703170	AGAAAATAGTATGTA[C/T]AGTATACTACCATTT	161436
rs574411021	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88622784	TTTTATTATAAACAA[A/C]TACCAAGTTATAAGC	161436
rs574432590	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88655382	AGCAATGAGAAAGGA[G/T]TCCCTCTTTAATAAA	161436
rs574435014	snp	A/C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88763436	TCTAGACACACACAC[A/C/T]CCCCCAAGACTAAAC	161436
rs574435394	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88709911	ATAAATTTTTCTTTG[C/T]TAGATATTTGGTTTT	161436
rs574436663	snp	A/T	0.0111196	0.0737302	intron-variant	EML5	GRCh38.p7	14:88651554	AATAAATAATTTTTT[A/T]AAAAAATCAATATAA	161436
rs574457049	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756652	GGTTGCAGGATATAC[A/G]ATCAACATAAAAAAT	161436
rs574504247	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88732459	TACCATGCTGTTTTG[G/T]TTACTATAGCCTTGT	161436
rs574507299	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88734004	ACCTAAAACAACCTA[C/T]ACGAAGTAAAAAAAA	161436
rs574516447	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88634128	ATCATGGGGGCAGAT[A/T]TCCCCCTTGCTGTTC	161436
rs574520273	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771469	TGCTTTCTGGAATTA[C/T]TGCTTCCTCACTACT	161436
rs574538039	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612128	GTGGAGAGATGCAGT[A/G]AGGCAGTTGTCATTA	161436
rs574631703	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88649699	ACAGTCATATGTAAA[A/G]CAATTTATCATAATG	161436
rs574697168	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672718	GACATCACCACTGAT[C/T]CCACAGAAATACAAA	161436
rs574698270	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737819	TGCTCAGCCAGTCTT[A/T]TAACACTTCAGTCTG	161436
rs574717412	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88776876	ACAGAGCAAGACCCC[A/G]TCTCAAAAATGAAAA	161436
rs574722069	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88729722	GTGCCACCATTCCCC[A/G]GCTTATTTTTGTATT	161436
rs574738481	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88687981	GAGGCTGAGGCAGGA[C/G]GATTTCTTGAGCCCA	161436
rs574754105	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88784869	AGAAAGGAAATCAGG[A/G]TATCAAGGAGATATC	161436
rs574757095	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88696559	AGATGCAAACCACCT[A/G]TGGTAACTGAGATGA	161436
rs574765490	in-del	-/A	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88771589	AAAGCAAAACTTCTC[-/A]AAAGAGGTGTCTCAT	161436
rs574773306	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88792761	TGCCCAGAGCCCTTC[A/G]CCCGCCTCGGCTCGC	161436
rs574773858	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793698	CCTGGTCCTAAGTGT[A/G]TGTTTTCTTAAGTGA	161436
rs574818191	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88747652	ATGAGCAAAGAATAC[A/G]AGACTATAAAAAGTA	161436
rs574859892	snp	A/C	0.0260105	0.111035	intron-variant	EML5	GRCh38.p7	14:88640145	CCCACTGATAGTGTT[A/C]GATCATCAAGGTAGA	161436
rs574860230	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88776687	GTAGTTCAAGACCAA[C/T]GTGCGTAACATGGCA	161436
rs574888873	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88780554	CAGGGCAGGGCAGCA[A/G]TTGATGTTTATAAAA	161436
rs574889054	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708798	ATTATATGCTCACAA[A/G]GTACCTTTTGATTAT	161436
rs574980621	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88681517	TTCCTCAGCTGTCTA[C/T]CCTTAGTTTTTAGTT	161436
rs574997366	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88700475	CTGAGTTATTTTCAG[G/T]AAACAAAGCATCAAA	161436
rs575032801	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88635585	TATATTCTAGCCTCT[G/T]ACCTTGATGAGTACA	161436
rs575033987	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88646230	AGTTAAACATCAATA[A/C]AAGTAAATGTGCTAT	161436
rs575078092	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88636565	ACTCAGGAGGCTGAG[A/G]CAGGAGAATGGCGTG	161436
rs575090800	in-del	-/A	0.00280898	0.0373711	intron-variant	EML5	GRCh38.p7	14:88649831	AAATGTTTTATAGGG[-/A]AAAAATACCTTAAAA	161436
rs575098395	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669499	ACTGCCTCTTTAGGT[C/G]GGACCCTGACCATAA	161436
rs575108020	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88738654	TCCCATTATAATAGA[C/T]ATTAGACTTATGAAA	161436
rs575120500	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88774066	AAGGTTGCAGAGAGC[C/T]GAGTTCATGCCACTG	161436
rs575127979	snp	A/G	0.00358779	0.0422022	intron-variant	EML5	GRCh38.p7	14:88789070	GGCCTGTCTCAGTTT[A/G]AAAAAAAAAAAAAGC	161436
rs575153339	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88781305	GTAGGGTAAAACTGC[A/T]GAACTTTCACAGTTC	161436
rs575201896	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710692	CTCAAGCTGACTCAC[A/G]AGTGCCTAGAAATAG	161436
rs575204689	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731479	ATCACTGATGGACAT[C/T]TGGGTTGGTTCCAAG	161436
rs575206502	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88724424	TTTGTGGTTCACTTT[C/T]AAAGGCATTTAATAA	161436
rs575228742	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788349	TTTTTCTTAAGAACA[C/T]GATTTACCACAAATA	161436
rs575253828	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88705294	CAAGCATACTTAATA[C/T]ACCAAGCATTTAATA	161436
rs575277016	snp	A/G	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88727396	TCTGTAGTGTGATAC[A/G]CTGCATTTTTTTTTT	161436
rs575282205	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654321	CTTGTCTTCTACTAG[C/T]TTTTGAATTTGTTTG	161436
rs575291981	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713499	TTTGTTTAGTTAGAG[C/T]CACGATCTTGCTCTT	161436
rs575348203	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88691185	TCTCCAGGAACAGAA[C/G]GACACACTAGGATCT	161436
rs575352020	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88678270	CAGGGAGAGGAACAC[A/C]CACTGGGGCCTCTTG	161436
rs575383283	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767303	GTCAGTTCTCAAAGC[A/G]CCTGATATGCAGGCA	161436
rs575385005	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88624097	GTTTTTGTTTTTTAA[A/G]TGGGGTCTCACTCTG	161436
rs575387399	in-del	-/TTC	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88764778	TGTTGTATTTTCACT[-/TTC]TTCTTCTTTTCATTT	161436
rs575404851	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88759846	CTGTCAGTTTTCCAC[A/C]GTAGTTGTACCATGT	161436
rs575404961	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88749921	CTGTGAAAAGTACTG[A/G]TTTAGAGCAGGGGTC	161436
rs575413367	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88684958	CTTTTGGCTCTTATA[C/T]ATTGAAATAATCAAT	161436
rs575438207	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88632277	TCCTGCCACCCTGCT[A/T]AACTGTTTTTTGCTT	161436
rs575456941	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613014	ATTGACTTGCTTAGT[C/T]GTATACTCAAATGAT	161436
rs575458933	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88677278	AAGCTGGACCCCTTC[C/G]TTACACCTTATACAA	161436
rs575492787	snp	C/T	0.00398564	0.0444627	intron-variant	EML5	GRCh38.p7	14:88623663	GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGT	161436
rs575530433	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88685532	TTGATTCCAGGACAA[A/C]CACAGATACCAAAGT	161436
rs575535263	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765579	ACTGGGCCCATCTAG[A/G]TAATTCAAGATACTC	161436
rs575549333	snp	A/G			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615588	TACCATCAAGTATTC[A/G]ATCCTTCCTTGAAAT	161436
rs575556337	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614497	GAATCTTCATATATC[C/T]TGTCAGACCAAATGG	161436
rs575574048	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772413	CAATAGCTTCCTACC[A/G]AATTAGAATGAAACC	161436
rs575581402	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88772702	AGGTTGCAGTGAGCC[A/G]AGATCCTGCCACTGC	161436
rs575587944	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88729349	CATTCTATGCTCTTA[C/T]CACAAGGGACAGCAA	161436
rs575589835	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88721166	GGATAGGAAGAATGA[A/G]TATCATGAAAATTGC	161436
rs575614280	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785194	GAAGCTGGAAAGGGT[C/T]GTGGAGGACTCAGGG	161436
rs575632171	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622391	ATATTGGAGGTTTAC[A/G]TACAGTATTTAGACA	161436
rs575674868	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88715835	ACCCGGCTAATCTTT[C/T]TGACGTTTTTAAATA	161436
rs575680343	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88654810	TCCGTTTGTCCAGAG[C/G]TGAGTTCAACTCCTG	161436
rs575681033	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629532	TAAAGATGAAACTAT[C/G]TTTATTAAGTATATT	161436
rs575698161	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668172	ATCACTTTTTGCTAG[G/T]TAGCAATTCTTTTTA	161436
rs575698328	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88676473	GCCCCCATGATTCAA[C/T]TACCTCCCACCAGGT	161436
rs575711458	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88733126	CAAAACTTAAAACAA[C/G]AAGTGAGGTCTCCAC	161436
rs575712099	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88723320	CACGGATGAACCTGG[G/T]GCACATTATGCTTAG	161436
rs575725613	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88754056	GCAGGAACATTGCTT[A/G]AGCCCAAGAGTATGA	161436
rs575728254	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779314	CAGAAGTTTAAATAT[A/G]GCACAGAAATATAGA	161436
rs575744118	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653721	TACTGAGGACTTTCA[A/C]ATCGATGTTTACCAG	161436
rs575755955	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721014	TAAATTATGAATGAA[C/T]TCCCATTCACAATTG	161436
rs575764745	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88778711	TTAAACCAGGGAAGC[A/G]GAGGTTGCAGTGAGC	161436
rs575801615	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88781168	AGATGACTGATACAA[A/T]TACAATGCTCATGCT	161436
rs575838185	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88707614	ATCAACGAAATTCTG[C/G]AGAAAAACTTTCATC	161436
rs575843124	snp	C/G	6.79521e-05	0.0058285	intron-variant	EML5	GRCh38.p7	14:88704851	AAATGAAAGATAGTT[C/G]TTTTATACCCGTGAA	161436
rs575851000	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88711710	GTACTCTGGGAGGCT[A/G]ACGTGGGGAGATCAC	161436
rs575873328	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88622982	TTTATTTAGCCTCTA[A/C]AATACATTACAATAC	161436
rs575879890	snp	C/G	1.66985e-05	0.00288946	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712399	TACTTGGGCCAAATT[C/G]CATTTACTTCAAGGC	161436
rs575958301	in-del	-/TGTTTGTT	0.406641	0.194842	intron-variant	EML5	GRCh38.p7	14:88745163	ATGGTCTAAATTGTG[-/TGTTTGTT]TGTTTGTGTGTGTGT	161436
rs575976873	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88762476	GATCATGCCATTGCA[C/T]TCCAGCCTAAGCAAC	161436
rs575979952	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88672637	AAAAAAATTAATAAA[A/G]TAGATCATTAGCTAG	161436
rs575988093	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88618508	TAAGTGGGGGAGGAA[A/C]GGGGAGCTGTAGGTC	161436
rs575990392	in-del	-/G	0.00318978	0.0398085	intron-variant	EML5	GRCh38.p7	14:88750452	TAAAAATACCTCACA[-/G]GGGTTACTGTGAAAA	161436
rs575992600	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88646489	AGAATGATAGAAGCC[C/T]TGCTTTTTTCCCCAA	161436
rs576033905	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668489	GTGAGGTGAATACAC[C/T]GAGAACCAGGAAGTG	161436
rs576052976	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88698895	ACATTGACTCATGTA[C/T]CAATCACAACAACTC	161436
rs576073686	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88730494	GAGAAAACAGACTTG[C/T]TTAAGACTGTTAGCC	161436
rs576090166	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766323	TCTTTCAAAAGCAAA[C/T]AGGAGAAATATTGCT	161436
rs576093198	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88769844	ATAACTTCTTACTCC[A/T]AGAGTGAGAAACTAG	161436
rs576097349	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88665053	AAGCATTAAGAATAT[A/G]ACGAAAACAGTTATC	161436
rs576155785	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88663078	TGGGAGCTTCAAAGA[A/G]TAATTGTTCCTTAGC	161436
rs576159407	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755810	TCACCCTGGGAAACA[C/T]AGCAAACCATTGTCT	161436
rs576169411	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88755095	TGGTGTGAGCCACCA[C/T]GCCCAGCAGGTAATT	161436
rs576173594	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657968	GTACTTATTTAAAAT[G/T]CAGATATTTTTCATT	161436
rs576176077	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88701899	AGTAAAGTACTTACA[A/C]AAAGGAAGAATCTAT	161436
rs576222245	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708905	TCTCAGAGAAAAAAT[G/T]TATCAAGACAAACTA	161436
rs576266275	snp	C/T	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88693464	TCACTTCCACAAGAA[C/T]AGTATGGCGAACCGC	161436
rs576278880	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88692783	TTGTAAACGCATATG[C/T]TGTTATCTGATGAGT	161436
rs576287742	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88708242	ATAAATGGGTATCTT[A/C]AAAGTGAACCTAGAT	161436
rs576300182	in-del	-/CA	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88674343	GAGATTTAATTGACT[-/CA]CAGTTCTGTATTTCT	161436
rs576308216	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88619211	TCTCTACTAAAAATA[C/T]AAAATTAGCCAGGCA	161436
rs576314034	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88656137	TACCCAAAGGATTAT[A/T]AATCATTCTACTATA	161436
rs576363066	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88749274	TAAGTTAGAAGACAA[C/T]GGACAAACAGTTTAA	161436
rs576370727	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761756	TTCTGGTCCTAGATC[A/C]TTGAGGAATCACCAC	161436
rs576386275	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706984	CAGTTGTTCCAACAA[C/T]GTCCTTTATAATCAT	161436
rs576414677	in-del	-/AATAATAATAATAAC			intron-variant	EML5	GRCh38.p7	14:88686400	TAGAACTCAAGGTAT[-/AATAATAATAATAAC]AATAATAATAATAAT	161436
rs576432253	snp	A/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88665739	AAGAGGGAAGGGAAG[A/G]CAGGTAAGTAAGTAA	161436
rs576439962	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88638431	GCAGGGTTCTACCCC[A/G]CCCAGTCTAGTTATT	161436
rs576448125	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88706174	ACTTATGAGGCCAGA[A/T]TATACTTTAATATAA	161436
rs576453458	snp	C/T	0.000182614	0.00955371	intron-variant	EML5	GRCh38.p7	14:88688502	AATATTATGAAAGTA[C/T]CACTTTCAAAATGTA	161436
rs576483095	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88714084	CTCAAGCTGTCGGTC[C/T]ACTGTGGCCTCCCAA	161436
rs576516129	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751939	ATTTAAATAAGGAGA[C/T]AATAATAGCATCTAT	161436
rs576532016	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729877	TGTTTTTTGTTTTTT[G/T]TTTTTGTTTTTTTAA	161436
rs576535238	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88686747	GTCTAGGGGTTCAAG[C/G]TTTCAGTGAGTTATG	161436
rs576556137	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88641231	TTCTAAAAAATAGAG[A/G]AGTGGGCACTCCTCT	161436
rs576556390	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88783122	GAAAGAAAAGAAAAT[A/G]CCTGGACGTCCAGGT	161436
rs576570096	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88714570	ACACACACACAAAAA[A/T]GGTAACTGTGAAGTG	161436
rs576590312	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88685978	ACTTGTCCTAGGGAG[G/T]CTTCAGCAACATATT	161436
rs576592736	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88791518	CATTTCAAATATACC[G/T]CTCACTAAAGAAATG	161436
rs576626588	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88683938	ACTTACATTTAACAA[C/T]GTACTGGAGGTTCTA	161436
rs576635624	snp	G/T	0.000399281	0.0141238	intron-variant, missense	EML5	GRCh38.p7	14:88616564	ACTCGAGGGAGAGGA[G/T]TTGTTTCTAATAGCT	161436
rs576642337	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88690517	AGTGACCTTGTAAGA[A/G]CAGCTGGGTGGAGTG	161436
rs576645342	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88642743	TTGAAATATTACTAG[A/G]AAGTTCTGAAATATG	161436
rs576664268	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88736282	GGGATTACGGGCGTG[A/G]GCCACAGTGCCTGGC	161436
rs576706498	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88648823	ATTTCTGGTAAAATA[A/G]TATAAGATTTTATGG	161436
rs576734834	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645163	TCCCAGTAACTGGAA[C/T]AACAAGCGTGCACCA	161436
rs576739592	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88782375	TTCAGCCTGATGATG[C/T]AGTAGAAAAGAAAAA	161436
rs576762637	snp	C/T	5.04325e-05	0.00502132	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696917	TGGTTTAATGGTCTC[C/T]GTATCCCATATATGA	161436
rs576788234	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88641851	TCAGAAAAGTAAAAA[G/T]AAAATTATAAGTATA	161436
rs576791472	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88791104	TTCTTATCTTTACTC[C/T]ATCTTGCCCTACCTC	161436
rs576792841	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88696191	TATATATATATTTCC[C/T]TCTGAACTCTACTAT	161436
rs576814434	snp	G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88657803	AATATTAGAAGAGGT[G/T]TTACCTCTGTGTGGT	161436
rs576818910	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88776898	AAATGAAAAAACAGA[A/C]ACAACAACCAAAACA	161436
rs576831556	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88703218	AAATTGTATACTATA[A/G]AACAAAAACAATTGC	161436
rs576836537	snp	G/T	0	0	intron-variant	EML5	GRCh38.p7	14:88744654	ACATGCAAAACATTT[G/T]GTTACAAAAGCAAAC	161436
rs576892371	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613476	AATTTAGTTCAGCCA[C/T]TTTACAAGGAAATAA	161436
rs576900581	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88675930	TAAAACATAAGAAGA[A/G]TCACCTTTGCTCCAG	161436
rs576904142	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88756823	CCCACTGAAGGACAT[C/T]TTAAAAGATCTAAAT	161436
rs576907715	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88747707	CGGAACTTCCAGAAA[C/T]AAAAAATAAAATAAG	161436
rs576915938	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726981	TCAAGCAATCCTCTA[A/G]CCTCAGCCTCATGAG	161436
rs576917227	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88738687	ATCTTTCTCCTAACA[A/G]TGAACCTAAACTCTT	161436
rs576920550	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88734040	AGTAACAAACTATTG[A/T]AATTACTTGCAATTT	161436
rs576930620	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88723424	TAGCAGAGAGTAGAT[G/T]GGTGGTTAACAGGGA	161436
rs576959828	snp	G/T	0.0023933	0.0345097	intron-variant	EML5	GRCh38.p7	14:88746990	CTTCAGGGTTGGCTG[G/T]GTCTTCAAGCAACTT	161436
rs576960815	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619821	AGGCGCCTGCCACCA[C/T]GCCCGGCTGATTTTT	161436
rs576961182	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88779478	CGTCTTTCATTTACA[A/T]CATCCCCAAGAAAAT	161436
rs577038193	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88771511	ATTACCATTCAAATA[C/T]ACCCATTAAAAAACA	161436
rs577046011	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88666571	TAGGCCATTATTAAA[A/G]GTAGGAAGATACATC	161436
rs577057619	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784564	AATTCCTAGACATAT[A/G]CAACCTACCAAGATT	161436
rs577081255	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88629669	CATGGCAGGCATGTT[A/C]CTGGGGACATCGCAT	161436
rs577081287	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88639220	AATATGGTACTCCTG[A/G]ACTGACCCAGATAGA	161436
rs577109219	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88645555	TAATATTTCTATGAA[C/T]GTTCCACACTGTTAG	161436
rs577112623	snp	A/G	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88628653	ATTATAAATGTTATA[A/G]ATGTTTTAAAAATAG	161436
rs577116446	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88731531	CCACAATAAACATAC[A/G]TGTGCATGTGTCTTT	161436
rs577141501	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88760434	CTTTTCTCCATTGAC[G/T]TCCCCAAGCACTTTT	161436
rs577178799	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762582	GAGACTTTAATACCC[C/T]GCTGTCAATATTAGA	161436
rs577196605	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88784976	AATGGATAAAGAAAA[C/T]GTGGTATATATACAC	161436
rs577234914	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88740657	TTTGATGCTATATTA[A/G]AGCAGTGAGCTAAAA	161436
rs577235252	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	EML5	GRCh38.p7	14:88793840	TCACCAACAGTTACT[C/G]TTAATTAAATAAATT	161436
rs577293187	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88737936	TCTTCAATATACTTA[C/T]AATATCATTAAAAAG	161436
rs577311207	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88651284	GGGTTGAAATTGTAA[A/T]GTAAATTGAGAACAA	161436
rs577313813	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88631537	ACTTTGAGAAGCTGA[A/G]GCGGGTGGATAACCT	161436
rs577320597	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88725711	GTGAAGAAAGGTCTT[C/G]AGGGAAACCAAACAG	161436
rs577324490	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88688531	TACTCAATTATAAAG[A/G]AGCAAAGTTTCTTTT	161436
rs577343756	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88764877	AGAGAACATACTCTA[C/T]ATGATTTCAATTCTT	161436
rs577354656	in-del	-/TT	0.00755907	0.0610114	intron-variant	EML5	GRCh38.p7	14:88661467	GATATGATATATAAC[-/TT]AATGTATGGGATTAT	161436
rs577355037	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88743279	GATATTGAATGGTCC[C/T]AAAACAAAGAAATAG	161436
rs577363273	snp	G/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88695091	GCCTATCATACAGTA[G/T]AACACATTCTAACTG	161436
rs577393024	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88674428	ACCTTCTTCACAGGG[C/G]AGCAGGATGGAGTGA	161436
rs577429514	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88760636	TCCAAATTGCTTTGG[C/T]TATTCTAATTACTTC	161436
rs577435427	snp	A/C	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88663194	TCAGTATGATGTTTA[A/C]GTTTTATGGGAAAAA	161436
rs577441923	snp	C/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88726060	ATCTATAATTCAACA[C/G]AAAATGTTAACTGCT	161436
rs577470016	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767384	GCCCTTCTTGAGCTC[C/T]GTACCCCCTACAATT	161436
rs577503685	snp	A/G/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88673477	AGCACAAGACAAGGA[A/G/T]GCCTTCTCTCACCAC	161436
rs577504317	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88682208	AATAAAATACCTCTG[C/T]AACAACTTTAGCTCC	161436
rs577509363	snp	A/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88624877	GGTCGGAGAGGACAC[A/T]CTGTGTAGCCTAGAA	161436
rs577541281	snp	C/G	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88771352	ACTAATCTAACTGTA[C/G]TGGCAGACTCTGACT	161436
rs577544976	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612293	TAGTTTGAAAAGCAT[A/G]ATTATACAGGCCTCT	161436
rs577551218	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88718039	TGTGGTGCTGATGGA[C/T]TACAGATGGTGGGTT	161436
rs577566390	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88773469	TGTCATATAACGCAT[A/T]ATAGTAAATGAGTGG	161436
rs577631207	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88789195	AACTTAGTCTTAAAT[C/T]TAGACTAGAGATTTT	161436
rs577653417	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88720673	CAGCCAATATCATAC[C/T]GAATGTGCAAAAGCT	161436
rs577657412	snp	C/T	2.32253e-05	0.00340765	intron-variant	EML5	GRCh38.p7	14:88712491	CTTTCCTCCTAAAAA[C/T]AAATCAGAGTCTTAA	161436
rs577658978	snp	C/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88640577	GTTAAGAGGAAAGCT[C/T]ACAGTGCTAAATGCC	161436
rs577661650	in-del	-/G	0.00119737	0.0244387	intron-variant	EML5	GRCh38.p7	14:88675924	TTTGCTAAAACATAA[-/G]GAAGAGTCACCTTTG	161436
rs577665070	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88788471	AGTGTGGTATACTTT[C/T]CAAAATATTTCAGAT	161436
rs577673047	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88647671	ACTCAGCCTAGGTAA[C/T]AGAGTGAGACCGTCT	161436
rs577674192	snp	A/T	0.0252325	0.109451	intron-variant	EML5	GRCh38.p7	14:88640150	TGATAGTGTTAGATC[A/T]TCAAGGTAGAAAACT	161436
rs577680649	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88619554	CATAATTAATAAGCT[A/C]ACAATTCATTAAGAT	161436
rs577744014	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88761893	TCACCATTCTAACTC[A/G]TATGAGATGATATCA	161436
rs577769840	in-del	-/ATG	0.00199481	0.0315187	intron-variant	EML5	GRCh38.p7	14:88666618	AGAACCATATATGAA[-/ATG]ATATTTTTATTATTA	161436
rs577783969	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88684466	TGAGCCACCGCGCCC[A/G]GCCTGTTTTATTATT	161436
rs577784487	snp	C/T	0.00159617	0.0282053	intron-variant	EML5	GRCh38.p7	14:88719182	CTTGATCTCAGGAGT[C/T]TGAGATCAACTGGGC	161436
rs577789982	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88647177	ACCAGCCTGGCCAAC[A/G]TGGTGAAATCCCGTC	161436
rs577790492	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88742376	TAATTTGTGTTTAAA[C/T]AGCTATGTATGGTTG	161436
rs577813305	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88683253	AGAACCAGTAAACTC[A/G]CAGAGATAGCTGGGA	161436
rs577817699	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88654464	GCTGTGTCCCAGAGA[C/T]TCTGGTATGCTGTAT	161436
rs577861608	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88707766	GTAGCTTAATATAAG[A/T]CACTAATTTAACTTC	161436
rs577874420	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88729777	TGTTGGCCAGGCTGG[C/T]CTTGAACTCTTGGCC	161436
rs577895603	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88713083	ACTAATTCCCTAAGC[A/G]TCACAACAAATAAAG	161436
rs577896423	in-del	-/AACA	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88716732	TGTCCACTGCTCACC[-/AACA]CACACACACACACAC	161436
rs577897811	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88736093	GCAACCTTCGCCTCC[C/T]GGGTTCAAGCGATTC	161436
rs577919273	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88669301	CCTGGGGGAAGGGAC[A/G]GCTGTCATCACTTTG	161436
rs577922328	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88713387	ACAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA	161436
rs577953209	snp	A/G	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88714745	TAAGGCAGCCTTATT[A/G]TATTATATTGTAGAA	161436
rs577989391	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88668592	TGTCATGTGAACACA[C/T]AGAGAAGGGCGCCTC	161436
rs577994227	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615073	TGTTCATCATACTAC[C/T]TTTCCATTAGTGAGG	161436
rs578040034	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700784	CCGGAAAGGTTAGAT[C/T]GTAAACCATTAAATA	161436
rs578055483	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	EML5	GRCh38.p7	14:88766750	AATAAAAACTTACCA[A/G]TTTTGCAGCTTGAGG	161436
rs578059638	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88727495	CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT	161436
rs578068792	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88777518	AAAACTCACTGGTAA[C/T]AGTAAGTACACAGAA	161436
rs578083539	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88751755	TAAGAAGCAGACAAG[A/G]AAAGACTCCTTTAAA	161436
rs578102905	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88751217	CTACCTCCTCTTCTA[C/G]CTTTTTATCATTTTT	161436
rs578107927	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88772821	TTTTCCTTTTGTTCA[A/C]TACACTCCAGCTACA	161436
rs578114621	in-del	-/TTT	0.00279162	0.0372561	intron-variant	EML5	GRCh38.p7	14:88732518	CCTTCAGTGTTGTTC[-/TTT]TTTTGGCTTAGGATT	161436
rs578117755	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88753977	GATCCCATCTCTACC[-/A]AAAAAAAAAATTAGC	161436
rs578173483	snp	A/C	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88705324	ATAAAAAAAATTTTA[A/C]ACAAGTGTACTCTAA	161436
rs578189762	snp	C/T	3.3248e-05	0.00407712	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704932	GTAGCACTTTTTTGT[C/T]TCTCTTTGCACTGTT	161436
rs578211651	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88691365	CCTACATAATACCCT[C/T]GATTTTGTCCTTTGG	161436
rs578224620	snp	G/T	0.000798403	0.0199641	intron-variant	EML5	GRCh38.p7	14:88760278	AAACTTTTATAGTTT[G/T]TCTTACATTTAAAGC	161436
rs578245938	snp	A/G	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88654485	TATGCTGTATTCTTT[A/G]TTCTCATTGGTTTCA	161436
rs578261119	snp	C/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88653755	TATTGGCCTGAAATT[C/T]TCTTTTTTTGTTGTG	161436
rs578262040	snp	A/T	0.000399281	0.0141238	intron-variant	EML5	GRCh38.p7	14:88662081	TTCTAGATGCTAAGC[A/T]TACAGTGTTAATAAT	161436
rs745338717	snp	C/T	5.09533e-05	0.00504718	intron-variant	EML5	GRCh38.p7	14:88644409	GATACATTTCAGTAA[C/T]ACTGGAGAGTGAGTT	161436
rs745340216	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88618428	ATTGCTACTTGATTT[A/G]CATGTCTAACATTAT	161436
rs745342891	snp	A/G	6.1192e-05	0.00553103	intron-variant	EML5	GRCh38.p7	14:88726695	TGTAAAATTTAATTT[A/G]AAAAATAAAAAAGGT	161436
rs745343375	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88696779	TTAGGTAACACTGAC[-/TT]AGATTAAAATGCTAT	161436
rs745370830	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88759810	AGGATAGGGTGGGTC[C/T]GTGTTTAGATTTATA	161436
rs745391671	snp	A/G	1.67489e-05	0.00289381	intron-variant	EML5	GRCh38.p7	14:88664668	TTTCTATCTTTGGAA[A/G]TACTTTTTTACACTC	161436
rs745407209	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88673345	TCAACATCCCATCAC[A/G]TTAAAAATTCTCAAT	161436
rs745409216	snp	A/C	2.89205e-05	0.00380256	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726549	ACCATACCTTACTCT[A/C]AGTACAGTGAATGAG	161436
rs745461177	snp	C/G	1.72056e-05	0.00293301	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754581	TAAAACTGATATGGT[C/G]TGCACAGTGTATGAA	161436
rs745505691	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88709979	CAAATATAAATTTTC[A/G]TTTGTCAACAAGAAG	161436
rs745534847	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747198	AGGTGGATTGCTTGA[A/G]GCCAGGAGATTGAGA	161436
rs745556375	in-del	-/AAG	0.000248067	0.0111343	intron-variant	EML5	GRCh38.p7	14:88705623	AATGTTACTTGTTTA[-/AAG]AAGATTCATTTTCAA	161436
rs745570586	snp	A/C	1.81381e-05	0.00301143	intron-variant	EML5	GRCh38.p7	14:88618862	ACATGAAGTATTATA[A/C]ATACTTAAGATCAGT	161436
rs745577292	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88779050	TTTCTTCTGGCGCAA[A/G]CAACCATCAATGTTC	161436
rs745579898	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88659900	CTGAATACCACAATA[-/T]CATTTCAGTGCCATA	161436
rs745593036	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725829	AAGGAAGGAGATTAA[C/T]ATGAGAGCTATCTCA	161436
rs745600689	snp	A/T	3.59428e-05	0.00423912	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695420	AACAGTATGGCTATC[A/T]TCTATGCCAACTGAT	161436
rs745611414	in-del	-/T	0.00602223	0.0545422	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792270	AACTCCGGGAGCGGC[-/T]TGCAGGGTGACGGCG	161436
rs745615658	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713978	GAATAGCTGGGACCA[C/T]AGGTGCATACCACCA	161436
rs745629424	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88699508	AGACAGCTGTTTAGA[C/T]AGCCTACAGGCTATT	161436
rs745631079	snp	A/G	8.66341e-05	0.006581	intron-variant	EML5	GRCh38.p7	14:88618216	TTGCCTTGTGAATAT[A/G]TAAGTATTTACCTAG	161436
rs745642474	snp	G/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793046	AGCCGAGAAGAGGCT[G/T]GAGTTCGCGGGGCCA	161436
rs745644811	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88751931	CATCAAATATTTAAA[G/T]AAGGAGATAATAATA	161436
rs745654746	snp	A/C	1.75016e-05	0.00295813	intron-variant	EML5	GRCh38.p7	14:88740595	GTATATAGTATAATC[A/C]AATTACCAAAGAATT	161436
rs745658625	snp	C/T	1.99332e-05	0.00315693	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687306	GAGCTACTATACCAT[C/T]TTTTCCTCCAGTTAC	161436
rs745666362	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88700748	CAAATGAGGACAAAC[A/G]TTTCTCAGAAAGTGC	161436
rs745699898	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88753094	CAACACTTAAGCTGC[A/T]GGTGTCAAAGAATAT	161436
rs745735896	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631736	GATTGTGCCATTGCA[C/T]TCCAGCCTGGGCAAC	161436
rs745790884	snp	C/T	1.6698e-05	0.00288941	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624974	AGAGGACTCACGGCC[C/T]TTCCTTTCCCCCAGT	161436
rs745809644	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772471	CCTTTGTAAGATATA[C/T]CTTCGGCCGGACGAG	161436
rs745824400	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88738061	CAATATAAAGACACC[A/G]TGTACCTCACAATGT	161436
rs745829475	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88785286	CACAACAGGGTGACT[A/G]TAGTCAGTAATAATT	161436
rs745830584	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88716732	TGTCCACTGCTCACC[-/AA]CACACACACACACAC	161436
rs745844412	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88752215	TATATAGAAGAAATT[C/T]CTCAGCAATGCAATA	161436
rs745847086	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88672460	AGAAAGATCTCAAAT[A/T]GACACCCTAATATCA	161436
rs745856524	snp	C/T	1.77662e-05	0.0029804	intron-variant	EML5	GRCh38.p7	14:88704988	GTAAACCTTTAAAAA[C/T]GTATACAAGTAGAAA	161436
rs745860704	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88633505	GTTTTTTGTACCCTT[G/T]TCTTGACATGATGGA	161436
rs745874047	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88743570	CAGCAGTCACAGTTT[C/T]AAAATGTGAAAATAA	161436
rs745885270	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725379	AAGGGGAGTCAGCAC[A/G]TGTAGAGGCTCAGAA	161436
rs745892522	snp	A/G	1.66222e-05	0.00288285	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616159	GCAGTCATCACCTCC[A/G]GCACTAACAACATGT	161436
rs745898012	in-del	-/ACTAA	3.54497e-05	0.00420994	intron-variant	EML5	GRCh38.p7	14:88657358	TTTTCTTCATCTAAT[-/ACTAA]ACTAAATTATTACCT	161436
rs745902551	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88776044	CTATGAGTCTGCAAC[A/G]ATTACAGCATTACTG	161436
rs745909109	snp	A/T	1.6832e-05	0.00290099	intron-variant	EML5	GRCh38.p7	14:88684976	TGAAATAATCAATTG[A/T]ATGTAAAGAAAAAAA	161436
rs745910542	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690502	GAAGGCAGAGTCATT[A/G]GTGACCTTGTAAGAG	161436
rs745913839	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88789006	ATTTCAAAGATACAG[C/T]GAGCAGTGATTGCAC	161436
rs745942436	snp	C/T	1.65952e-05	0.00288051	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738913	TTCCCTGAGATCAAT[C/T]ACAGTAATTGGTTTA	161436
rs745967154	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638289	AAAGAATACAGGTAT[A/G]TTTCAAAACAGCTCA	161436
rs746003385	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643856	GGTTGGGGAGGGAAC[A/G]ACAGCAATCACCATC	161436
rs746020536	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88623624	TCACCATATTGGCCA[A/G]GCTGATCCCAAACTC	161436
rs746063069	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88713011	AAAAACTTTTGGGGA[C/G]ATGCATTAATTGAAT	161436
rs746073929	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663540	AACATTTATCAAACA[C/T]ATTAAACTCAGTCAT	161436
rs746074720	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88677586	ATCCAGAATCTACAA[G/T]GAACTTAAACAAATT	161436
rs746076608	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88728143	AGATTCAACCAACCA[C/T]GGAAGGAAAATGTAG	161436
rs746109841	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765484	GTTCTTCTCAAGCTT[C/T]GAATCTTTCTGACTT	161436
rs746146734	snp	G/T	7.52587e-05	0.00613382	intron-variant	EML5	GRCh38.p7	14:88702416	CAAAGGTGTAGCTTA[G/T]CTGGCTTATTGTCAG	161436
rs746149920	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717200	TAGCTCAGCAGAAGA[C/T]AGGAAATGGAGGTAA	161436
rs746160388	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660853	ATGATTTAAAATGCA[C/T]ATATATTCTGCTACG	161436
rs746162842	snp	C/T	3.31263e-05	0.00406965	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621207	AGTCCCCAGATTGGC[C/T]CATCCACATGACCGT	161436
rs746163917	snp	C/G	3.32912e-05	0.00407976	intron-variant	EML5	GRCh38.p7	14:88627058	GCACCTGACAAGATA[C/G]AACAAAATTATCTAG	161436
rs746165742	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88735008	ATACAGAACACTGTG[A/T]GATAACAGTATTGTG	161436
rs746183766	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758346	TACAGGCATGCACCA[C/T]CACGCCCAGCTAATT	161436
rs746192289	snp	C/T	0.000135639	0.00823415	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694376	GCACATAGGGGTTCA[C/T]CTTTACAACAAAAAT	161436
rs746197204	snp	A/C	2.47094e-05	0.00351484	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618731	GCTGATTCTGTTAAG[A/C]GTGGGGCCCAGCGTT	161436
rs746200782	snp	A/G	3.34253e-05	0.00408797	intron-variant	EML5	GRCh38.p7	14:88746311	CAAGAAGTCCAGGAA[A/G]GAATAAAAAGGCAAA	161436
rs746230803	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88769125	TTAAAATTTTGTAGT[G/T]GGTGAGGGCATTGAT	161436
rs746246180	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88669664	TAGTCTTTCCCTCTA[C/T]CAGCTCTGAGGAATC	161436
rs746247376	snp	A/C	2.66642e-05	0.00365122	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706416	GCCAATATATTTTCT[A/C]AACTTGGCCCCTATA	161436
rs746283830	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88770460	TTTCACATCATTTGT[A/T]GACAAGAGACCATTC	161436
rs746288341	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704322	CTTTGCCTTCTGCCA[C/T]GAGTAAAAGCTTCTT	161436
rs746321682	snp	A/C	2.14894e-05	0.00327784	intron-variant	EML5	GRCh38.p7	14:88740359	AGTAATACACATGAA[A/C]GTGTTTAAAATACTT	161436
rs746324282	snp	C/G	1.69312e-05	0.00290952	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706274	CTTGGGGTGCTATGT[C/G]AACAGCATCTTTCAG	161436
rs746338611	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615098	GTGAGGCTACAGTTA[C/T]GTTTTAAATGTGCGA	161436
rs746367308	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88705272	AATCCTATAGGCAAA[C/T]AGAAGGCAAGCATAC	161436
rs746370942	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652703	TTCCTTCTTACTGTT[C/T]CTGGATCTTTTCCTT	161436
rs746395722	snp	A/T	0.000298711	0.0122174	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616232	TGACCCAAGAACCTT[A/T]TGTGTTTTGCCTAAA	161436
rs746402547	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88757336	TGTCAACTCAAAATG[C/G]ATCAGAAGCTAAAAT	161436
rs746414203	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88741707	TGGGCCACATGGTAG[C/G]ATCCCATCTCTAAAA	161436
rs746422552	snp	A/G	4.62246e-05	0.0048073	intron-variant	EML5	GRCh38.p7	14:88657512	CATAGCCTACAATAA[A/G]AATATACGAGTAATT	161436
rs746434024	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88788154	CCTACCAGAGCTTAA[A/G]AAGTTGCTACTCTGA	161436
rs746438466	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88715253	AACAGAATTAATGCC[A/G]TTTCAAACATGTCTA	161436
rs746438493	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88636993	TGTAACTGGCTAAAA[C/T]AGTACAAAATCAAAC	161436
rs746439896	in-del	-/TATATG			intron-variant	EML5	GRCh38.p7	14:88706484	CAAAATACCATTTCA[-/TATATG]AACAATTTTTATATA	161436
rs746445687	in-del	-/AG	0.000123332	0.0078518	intron-variant	EML5	GRCh38.p7	14:88712497	TCCTAAAAATAAATC[-/AG]AGTCTTAATTTAAAA	161436
rs746472023	snp	C/G	1.6676e-05	0.00288751	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88664515	ATCCCAATCAATATG[C/G]GTTATGTAACTGGTA	161436
rs746479453	snp	A/G	1.88998e-05	0.00307401	intron-variant	EML5	GRCh38.p7	14:88642884	GGATGGAGAATCAGG[A/G]TTTCCTACCTGTAGC	161436
rs746484150	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88685174	AGATGTTCTTTTAGA[A/C]ATACAGTTACTATAA	161436
rs746485394	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88783878	TTTTTCCTCAGCACA[C/T]GGATTATTCTCAAGG	161436
rs746487559	in-del	-/TTTCAC			intron-variant	EML5	GRCh38.p7	14:88645053	CTTTTTTAGACCAAG[-/TTTCAC]TTTCACTTTGTCACC	161436
rs746509622	snp	A/G	3.41559e-05	0.00413241	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754576	TCCTTTAAAACTGAT[A/G]TGGTCTGCACAGTGT	161436
rs746515867	snp	A/G	2.96362e-05	0.00384932	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715165	AATTGCCTCCTTCCT[A/G]TCTTTAATATGTACA	161436
rs746524854	snp	A/C	8.5907e-05	0.00655333	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88694362	AATTAGTTTATCAGG[A/C]ACATAGGGGTTCATC	161436
rs746526204	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88756613	AAACAACCAAAAAAT[-/G]AAGAGCTAATATGAA	161436
rs746527326	snp	C/T	1.65858e-05	0.00287969	intron-variant	EML5	GRCh38.p7	14:88661874	TGGATTATCCAAACC[C/T]AAAGTATTAACAACC	161436
rs746530740	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88792924	CAGCCTGGCGGACCC[A/G]CGCCGCGCACCCCGA	161436
rs746535433	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88686577	GTAATTTCAGTGCTT[C/T]GGGAGGCCAAGTTTA	161436
rs746537566	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88671465	ACACTGAAGTACGAA[A/G]ATCAATGATACTACG	161436
rs746565103	snp	C/G	1.66854e-05	0.00288833	intron-variant	EML5	GRCh38.p7	14:88746304	TTATGTCCAAGAAGT[C/G]CAGGAAGGAATAAAA	161436
rs746598230	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88719749	TTTCCAATGCTACTC[C/G]CCTTGCAGAAATACC	161436
rs746609907	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88772389	TCATCATTTACCTCG[C/G]TAAAAACCCAATAGC	161436
rs746620613	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88617021	ATGGTAAGTTGTTTG[C/G]AGACCTGAATTTCAT	161436
rs746621483	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721444	ATGGAACAGAATAGA[A/G]AATTCAGAAATAAGA	161436
rs746624595	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757807	TTCCCTCTTTCCTTC[C/T]TTCCTTTTCTTGCTT	161436
rs746643084	snp	C/T	2.12705e-05	0.0032611	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618706	CAAAGCTTGGAATGT[C/T]TTTGCAGTAGCTGAT	161436
rs746649060	snp	A/G/T			intron-variant	EML5	GRCh38.p7	14:88633314	TTTTGTAGAGACAGG[A/G/T]TCTTGCTGTTGCCCA	161436
rs746655758	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88731889	GAAGTGTCTGTTCAT[A/G]TCCTTTTCCCACTTC	161436
rs746689373	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88663640	TTGAAGATATATTTC[A/G]TATCAAACAATGAGA	161436
rs746701235	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88790253	TTCAGATTTTACTCC[C/G]TCATTGAAACTTTTC	161436
rs746704990	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760984	ATATAACTAATTTAC[A/G]TATGTTGACCTGGTA	161436
rs746725134	snp	C/G	1.65614e-05	0.00287757	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688435	TGTCATTTTTCCCCA[C/G]TGTGCCTATGTAGCC	161436
rs746761315	snp	C/T	4.98004e-05	0.00498976	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616267	AATGACAGACAAGCT[C/T]AGGGCATTTGGTGCA	161436
rs746776715	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623212	GTAGAGATGGGGTTT[C/T]ACCATGTTGGCCAGG	161436
rs746779826	in-del	-/AATTGGT			intron-variant	EML5	GRCh38.p7	14:88634586	AACTATTATATACAA[-/AATTGGT]AATTGGTTTTATTAC	161436
rs746806407	snp	A/G	5.20567e-05	0.00510153	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740394	GTACTTACAGCATGG[A/G]CTCCTTGTATTGTTC	161436
rs746835391	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88749074	TCCACAAATTTAAGA[C/T]GTTCAACAAATCCCA	161436
rs746838186	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712939	GGATAATATATTTAC[A/G]TTAGGTAAGAGGACT	161436
rs746852173	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88765321	AAGTTCATTCAGAAC[A/G]TTAGCTGAATTCAAT	161436
rs746857435	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653509	TTTTAGCATGAAGGG[A/G]TGCTGAATTTTATCG	161436
rs746858288	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88750142	ACTTACTATAGACAG[C/G]TTATCAAATGGTGGT	161436
rs746866999	snp	C/T	1.83559e-05	0.00302945	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702553	GTCGATTATAAATGA[C/T]ACCCACTGCTGCCAC	161436
rs746879474	snp	G/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664537	TAACTGGTAGCTCCT[G/T]TGCATATTCCTACTC	161436
rs746899414	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88699409	CAACTCTGCATTAAT[A/G]TTATGCCTTGAATTG	161436
rs746899445	snp	C/T	1.71469e-05	0.002928	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622564	GTAATAACCACTTTC[C/T]GTTTTCTGCTGCACT	161436
rs746951504	snp	A/T	1.73123e-05	0.00294208	intron-variant	EML5	GRCh38.p7	14:88644388	GTTTTATAAAAAAGA[A/T]CTCTGGATACATTTC	161436
rs746959115	snp	A/T	1.65784e-05	0.00287905	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642990	CCTACAGTCTCTGCC[A/T]CGATAACCAAAAATG	161436
rs746972429	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88709056	TATTTTCACACAAGG[G/T]TAATATGATCTAAAT	161436
rs746977098	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630418	TCTCTGTAGTGAGTA[A/G]CTCCTTACTGCATAC	161436
rs746982423	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88751584	AATGTAGAAAATGGA[A/G]TATCTACAGAACATT	161436
rs747000181	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88782933	AAAAATACAGAATTA[A/G]TCAGGTGTGGTGGCA	161436
rs747000215	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647072	TGCAGACAGCTATAT[C/T]GCATAATATTAAAGG	161436
rs747009432	in-del	-/AA	0.000116803	0.00764119	intron-variant	EML5	GRCh38.p7	14:88627084	CTAGGTTATTACAAG[-/AA]AACCAAGCTAATCAA	161436
rs747031301	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88669599	TGATCTCCCAGGGAC[G/T]GAGCTCCTAGAGGGG	161436
rs747031491	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88649855	CTTAAAATACCATAA[A/G]GAATAAAATAAAGGG	161436
rs747043718	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88704261	CCTTCCCTTTCGATC[A/C]CTTTTTCCTTGCTCT	161436
rs747054035	snp	C/T	1.65723e-05	0.00287852	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621175	AAAGGAAAAAATCCC[C/T]GGAAGGATGTGTTGC	161436
rs747060696	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765996	ATAATTTCTTATGCC[C/T]GTCTTTACTGCAATC	161436
rs747064934	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88689712	ACGCTCCAGCCTGCG[A/T]GACAGAGCAAAACCC	161436
rs747076038	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88740317	AATATACTATATTAC[A/G]CAGTCTATCATTCTA	161436
rs747087051	snp	A/G/T	7.6402e-05	0.00618029	intron-variant	EML5	GRCh38.p7	14:88702406	TAAACTCAAACAAAG[A/G/T]TGTAGCTTATCTGGC	161436
rs747098774	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88705146	GAAAGAACAAACAAA[G/T]TCACATTTTCTACAT	161436
rs747098990	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88769208	TGCTGGAGGTGGAGC[A/C]TGATAGGAGATAACT	161436
rs747119302	snp	A/G	1.66056e-05	0.00288141	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714976	TTTCCCATTTCCATC[A/G]TTTGTCTGCAAATAT	161436
rs747121272	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88635594	GCCTCTTACCTTGAT[A/G]AGTACACTCCTATAA	161436
rs747157262	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88774779	TTCAGTGGTCTCATC[G/T]AGGTTCATGGCTTTA	161436
rs747180701	snp	C/G	2.614e-05	0.00361515	intron-variant	EML5	GRCh38.p7	14:88712500	TAAAAATAAATCAGA[C/G]TCTTAATTTAAAAAG	161436
rs747183491	snp	C/T	0.000105859	0.00727451	intron-variant	EML5	GRCh38.p7	14:88634536	ATAAATCTGTAAAAT[C/T]TGTAAAAACCCAAAT	161436
rs747188656	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675126	AGCTGTCAGTTGTTC[C/T]ACCATTCTGGGGTCT	161436
rs747209930	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88787986	TAGATTCCTGGGCTC[C/T]AACCCTAGAAGATTC	161436
rs747211395	snp	A/G	5.12125e-05	0.00506	intron-variant	EML5	GRCh38.p7	14:88620935	ACATCTTCTGCATTT[A/G]AAAAAAAAAAAAAAA	161436
rs747235310	snp	A/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621258	GCATTTTTCTCTCCA[A/G]CTTCGATTATTTCAG	161436
rs747242515	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690336	CTGGATTGAGAATAG[A/G]TACAAGGGAGGTCAA	161436
rs747247833	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88622909	CAGTCAAAATAAACA[-/T]CCAGTTTCAGTGAAT	161436
rs747253041	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88789044	CTATAGCCTGTGTGA[C/T]GCAGAGCAAGGGCCT	161436
rs747265094	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88775797	TGATTACAGCAAGCC[C/T]TGGGCAAGACAAAGT	161436
rs747267303	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88686259	AGAAAGGCCCAGAAG[C/T]CAGAGAGAGTGTGGT	161436
rs747277591	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88730882	ATGAAAACGTAAGGG[A/G]TTTAAAGCCTGTGCT	161436
rs747284745	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88694475	AATCTCTTGCCTAAT[C/T]CATACCCTATCTTGA	161436
rs747293706	snp	A/G	7.80732e-05	0.00624744	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627819	ATAGAAGGAGCTGTA[A/G]CTAAATAAAGATAGT	161436
rs747295706	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676465	AAAGACCTGCCCCCA[C/T]GATTCAATTACCTCC	161436
rs747312826	snp	G/T	1.67998e-05	0.00289821	intron-variant	EML5	GRCh38.p7	14:88625139	TATTCTGAAAAGGAG[G/T]GGGGGAGGGGGAGAC	161436
rs747315097	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88714679	ATATACAATTTTTAA[C/T]GTCAATTATACCTCA	161436
rs747335649	snp	A/G	2.33609e-05	0.00341759	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657474	GGTGTAACTGATTTC[A/G]TTCTCCCTTGTAACA	161436
rs747336807	in-del	-/AGA	4.26389e-05	0.0046171	intron-variant	EML5	GRCh38.p7	14:88618609	ACGAAATGTAAAAGC[-/AGA]AGAACTTGCCACCTG	161436
rs747337620	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88679606	CTGAAGCAGAAGAAT[C/T]GCTTGAACCTGGGAG	161436
rs747338542	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747990	TGAACCCTGAAAGAG[A/G]GGAAAACAAATAAAT	161436
rs747348618	in-del	-/A	2.31747e-05	0.00340394	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615785	TGTAATTCTGGTCTC[-/A]AAAGTTAATTTCTGT	161436
rs747353308	snp	C/T	0.000126662	0.00795708	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738900	ATCCCTGGTCTGTTT[C/T]CCTGAGATCAATCAC	161436
rs747390851	snp	A/C	2.83603e-05	0.00376555	intron-variant	EML5	GRCh38.p7	14:88649960	GGAAAAAAGTAGGAA[A/C]ACATATAAAAATTGA	161436
rs747392137	in-del	-/AT			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613842	GTTAAAAAAGTAAAC[-/AT]AGGGCAGATTCTATA	161436
rs747394848	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88681411	GTCAGGAGATTGAGA[A/C]CAGCCTGGCCAAGAT	161436
rs747471971	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88768791	GAAGTTATCTTTTCT[A/G]TTTATTTATTTAACC	161436
rs747472803	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88733478	TTCCAAATAAATTGC[C/G]CACCAATAACAGGAA	161436
rs747479298	snp	C/T	0.000251612	0.0112135	intron-variant	EML5	GRCh38.p7	14:88736581	CTAGTAAAAAGTAAA[C/T]TGTATTTAATATATA	161436
rs747493589	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88627366	CAAAACCAATCAAAT[A/C]ATTAATAATAAATAC	161436
rs747497592	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767698	AAGATTTTAATTTTT[G/T]TAAGAAGTGTTTTAT	161436
rs747512516	snp	C/T	1.66513e-05	0.00288537	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616116	GTAACATAGTCTGCT[C/T]TTCATGGGCTGAGAA	161436
rs747532574	snp	C/T	2.20495e-05	0.00332028	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615807	AATTTCTGTAGTCAT[C/T]TCAGCATCTCTCAGT	161436
rs747544811	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672266	AACCACATAACTACA[C/T]AGAAATTGAACAACC	161436
rs747558653	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88755484	CCCATAATTCGCAAA[A/C]AAAAATCTATGAGTC	161436
rs747601814	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88650794	GTACAGGCATGTACT[A/G]CCATTCTTGGCTAAT	161436
rs747616279	snp	A/T	1.70006e-05	0.00291548	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681894	GAGCCTCTTACCCTT[A/T]TTCAGCTTCCGGACA	161436
rs747616395	snp	A/G	1.79809e-05	0.00299836	intron-variant	EML5	GRCh38.p7	14:88618374	GAATTCCATTAGGTG[A/G]GAGACAAAATCCACA	161436
rs747622180	snp	A/C/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613899	CCCTCGTTGCTGGCT[A/C/G]ATACAGCGAGGTGGT	161436
rs747639628	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88628122	AAACAATTCAAAACA[A/T]ATGCATGTTTTATGT	161436
rs747658250	snp	C/T	1.67942e-05	0.00289772	intron-variant	EML5	GRCh38.p7	14:88746140	AACTCTCTTCTGGTC[C/T]TTCCCTTCCAGTACT	161436
rs747666185	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88663238	TAAAAACCATTTTCT[A/G]CTGCAGTCAACTTAT	161436
rs747689603	snp	C/T	1.77162e-05	0.0029762	intron-variant	EML5	GRCh38.p7	14:88706210	TTATTTGGGGGTTAC[C/T]GAAGAATTATTTGAC	161436
rs747704723	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88735131	ATTCCTAAATTTGAT[C/G]AGTGGTTCTCAAACT	161436
rs747714021	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88630218	ATTTTTAGTAGAGAT[-/G]GGGGTTTCTCCATGT	161436
rs747721679	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88645295	CCTCCCAAAGTGCTG[G/T]GATTAGAGGAGTGAG	161436
rs747742882	snp	A/G	3.46602e-05	0.0041628	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705552	ACATCAGACAGATCT[A/G]AATCTGATTCATCAC	161436
rs747789169	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769325	CCTCGCTTCCTTCTA[C/T]TCTAGCCATGTGAAG	161436
rs747794160	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671248	GGAGACACTAGGGGC[C/T]AATATTCAACATTCT	161436
rs747800772	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88754827	TATTTTTGTTGAGAC[-/AG]AGTCTCGTTCTGTCA	161436
rs747813859	snp	A/G	1.66743e-05	0.00288736	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625122	ACCTGTAAACGTCAA[A/G]TTATTCTGAAAAGGA	161436
rs747819890	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88669833	CACCTTATACAGGGG[C/T]GTTTCCACTGGTATC	161436
rs747820916	snp	A/G	1.65938e-05	0.00288039	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625019	CTCGCAGGGTGGTGT[A/G]CATGGCAAACACAGG	161436
rs747843552	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88741200	AAAAAGTTGGGAATC[A/G]GTTAGCAATGAAAAT	161436
rs747847316	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773840	ACTTATTACTGGGGC[C/T]GGGCATAGTGGCTCA	161436
rs747862444	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88756209	CTGGTTCAACATATG[A/C]AATCAACAAATATGG	161436
rs747863650	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88783468	GGACTGAAAATAAAA[-/G]GATGGAAAAAGATAT	161436
rs747875114	snp	A/G	0.00012078	0.00777017	intron-variant	EML5	GRCh38.p7	14:88649906	TTTCTTTTATAAAAC[A/G]CTTACCTTACTACTC	161436
rs747882967	snp	C/T	1.68818e-05	0.00290527	intron-variant	EML5	GRCh38.p7	14:88621357	CAGCTGCTTTTCTTC[C/T]TCATAATATAAAAAT	161436
rs747906089	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88636384	AGAGAAGCAAAAGGC[G/T]GGGCACGGTGGCTCA	161436
rs747909118	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88673894	AGAAACAAATGAAAT[A/G]ATTCCATGCTCATAC	161436
rs747913479	snp	G/T	1.65847e-05	0.0028796	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642971	TTAAATAGTGAACAT[G/T]ATTCCTACAGTCTCT	161436
rs747933385	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774446	GTTTTGTGTACCAAT[A/G]ATGACATGACTCATT	161436
rs747942095	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762491	CTCCAGCCTAAGCAA[C/T]AAGAGTGAAACTCCA	161436
rs747945293	snp	C/T	5.24315e-05	0.00511986	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702540	TGTGTGTTTTGCTGT[C/T]GATTATAAATGACAC	161436
rs747971407	snp	A/G	2.19493e-05	0.00331273	intron-variant	EML5	GRCh38.p7	14:88642850	GATCAAAATTTCTAA[A/G]TTAAAAAAATTGATA	161436
rs747977039	snp	A/G	1.66128e-05	0.00288204	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715017	AAGACCAGTCCAGAT[A/G]AGTGATGAAACTAAG	161436
rs748006854	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711010	TTTTTGTTTTTGCAT[A/G]GAGGTCAGTATGTGA	161436
rs748030628	snp	A/T	4.98376e-05	0.00499163	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746266	ATTCTTTGAATCAAG[A/T]CCAACTGAAACCAAG	161436
rs748043887	in-del	-/ACC			intron-variant	EML5	GRCh38.p7	14:88658076	CAGACTAAAAACAGT[-/ACC]ACCACTACAATTATT	161436
rs748049833	in-del	-/CA			intron-variant	EML5	GRCh38.p7	14:88632534	AGGCCTTCCTCCAGT[-/CA]CACTGACCTTCCAGT	161436
rs748057940	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711557	ATCACAACAGCAGCA[C/T]AGAGGAAACTGCCCC	161436
rs748072376	in-del	-/A	1.65891e-05	0.00287998	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88658221	AATGTCGGATTCTTC[-/A]CTATCACAAGGCCTT	161436
rs748082575	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88632581	CAGGGTTTATGCAGG[A/C]AAGATTTAATATAAG	161436
rs748089290	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644039	GCTTCATGAACCCTG[C/T]ACAGTGAATATATCG	161436
rs748089927	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660867	ACATATATTCTGCTA[C/T]GAAAGCAGAAAAAAA	161436
rs748092785	snp	A/G	7.70164e-05	0.00620502	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618665	CTGGAGATAACTGCT[A/G]TCTGCAGAGAAGTCC	161436
rs748101538	snp	A/G	5.69233e-05	0.00533464	intron-variant	EML5	GRCh38.p7	14:88661860	CAATGCTGTAAGTTT[A/G]GATTATCCAAACCTA	161436
rs748120829	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763847	CATTCAGTCTCTCAC[C/T]ATCAGGAATAAACTT	161436
rs748129381	in-del	-/CA	1.66793e-05	0.0028878	intron-variant	EML5	GRCh38.p7	14:88687166	ACACACATTAATGAG[-/CA]CAATTAATCTTTTTT	161436
rs748130196	in-del	-/TTT/TTTT			intron-variant	EML5	GRCh38.p7	14:88729870	CGGTCTTGTTTTTTG[-/TTT/TTTT]TTTTTTTTTTTTGTT	161436
rs748149185	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88662829	GATTACAGGCGTGAG[C/T]CACCATGCCCACTGA	161436
rs748162097	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715782	CACCTCATACCTCAG[C/T]CTCCCGAGTAGCTGG	161436
rs748186715	snp	C/G/T	2.5155e-05	0.00354639	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627787	AAGTCTGCTTGTTCA[C/G/T]TGCATCCCAGATGTG	161436
rs748201571	snp	A/C/T	8.32638e-05	0.00645181	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712370	CTACTGAATTTATAT[A/C/T]GTTGATATCTGAATA	161436
rs748231069	snp	C/T	1.84008e-05	0.00303316	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712465	TTTATTTCTTCTGTA[C/T]TTGTCACTTCCTTTC	161436
rs748232839	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767564	CATAATATTGTTACA[C/T]TGTAAGAGTTCTTAA	161436
rs748234941	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88753898	TCCAGCACTTTGGGA[A/G]GTCAACAACACTGGA	161436
rs748241855	snp	C/G	3.31417e-05	0.00407059	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658299	ATCTGTACCGCCTAG[C/G]GTAACCAACATGCTG	161436
rs748248298	snp	A/C	1.66924e-05	0.00288893	intron-variant	EML5	GRCh38.p7	14:88627085	CTAGGTTATTACAAG[A/C]ACCAAGCTAATCAAC	161436
rs748250759	snp	C/G	1.65671e-05	0.00287807	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740487	TCATCCCTTGCACAG[C/G]CTAGGCACAGTATTG	161436
rs748252491	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88648839	TATAAGATTTTATGG[C/T]CCATTTTAGAGGTTG	161436
rs748289832	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88754943	CTGAGTAGCTGGGAT[A/T]ACAGGCACCCGCCAC	161436
rs748293768	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617899	ATAGCATTCCTTTAG[A/G]TAGAGAATTAATAAC	161436
rs748295721	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88688140	AACAAAGAAAGGTCA[A/G]GATGACCCTAGCCCA	161436
rs748330127	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785864	GAGCCAGAGTGACTT[C/T]GTTAAACCGTAAGTC	161436
rs748352381	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720531	AAAACAAAGACCATA[C/T]GATTATCTTAATAGG	161436
rs748396293	snp	A/C/T	4.97231e-05	0.00498593	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616826	CAGGCACAGTTGACA[A/C/T]CAGCTTTCTCAGCAT	161436
rs748408783	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88649765	AAAATGCAACTCTTT[C/T]ATAGAATTTGTCCTA	161436
rs748414114	snp	A/C	2.28381e-05	0.00337913	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615793	CTGGTCTCAAAGTTA[A/C]TTTCTGTAGTCATCT	161436
rs748414291	snp	A/G	1.68547e-05	0.00290294	intron-variant	EML5	GRCh38.p7	14:88644539	AGTGGGGAGGAGGAA[A/G]GGCATGCAGCACTCA	161436
rs748424098	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88635395	CAAATGGTGAGAGGG[A/C]TTGGAACTTTGCCAC	161436
rs748426779	in-del	-/AAATC	0.000126664	0.00795713	intron-variant	EML5	GRCh38.p7	14:88620710	TTACAAATGGAAGTT[-/AAATC]AAGTATATACTAGAA	161436
rs748435505	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88740288	ATTTTCAAGCAACCA[A/C]ACTGACTAGAAACAA	161436
rs748475460	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88736124	TCCTGCCTCAGCCTC[C/G]CAAGTAGCTGGGATT	161436
rs748478280	in-del	-/CA	3.32386e-05	0.00407654	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622689	CTCAGTTCCTGATCC[-/CA]CAGTTTAACCGCTCC	161436
rs748479495	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88687073	TGATTCTGGTATCCA[-/G]GTTAAGTGATTTCTT	161436
rs748480041	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88738173	AATAAAATACCAATT[A/C]ACATTTACATGCTTA	161436
rs748484081	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88708842	AAAAATGATTCAGTA[A/G]TAAGAATAGTTAAGG	161436
rs748489963	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639871	CGGGCATGAGCCACC[A/G]TGCCCAGCAGGAATT	161436
rs748505867	snp	C/T	1.65734e-05	0.00287862	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736548	CACCTCGCCAACACA[C/T]ACTCCTTACAGACAA	161436
rs748508304	snp	A/G	5.2633e-05	0.00512969	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792453	GTGGCCCCGGTAGCC[A/G]TACACCCACTCGAGC	161436
rs748521356	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791887	AGCCCACCGCTTGCT[A/G]TGCTTCCATCAGTCC	161436
rs748529158	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88693106	TTTAATAGCATATGA[A/G]TAATTTTTTTTAATT	161436
rs748590843	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88747063	CGCAACTTTGATCTA[A/T]CCCTCAAAGAATTCC	161436
rs748614504	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780228	AAAGTGCTGAGATTA[C/T]AGGCATAAGTCACCA	161436
rs748629832	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641104	ACCAATAATGAGTTC[C/T]AAAATTGAATCAGTA	161436
rs748645015	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88681287	GACAAGGACTAATAG[C/T]GTAGAATTAAAAAAC	161436
rs748648066	snp	A/C/G	0.00027386	0.0116985	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792267	GCAAACTCCGGGAGC[A/C/G]GCTTGCAGGGTGACG	161436
rs748678392	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766706	ACCCACACCCTATTC[A/G]TACACTCCCTCCCCT	161436
rs748724855	snp	C/G	3.33339e-05	0.00408238	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705543	AGTTCTGGAACATCA[C/G]ACAGATCTGAATCTG	161436
rs748726565	snp	C/T	1.66175e-05	0.00288244	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624992	CCTTTCCCCCAGTCA[C/T]GATAAGTCCATCTCG	161436
rs748727637	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88763028	TAGAGAGAAATTTAT[-/A]AGCACTAAATGCCCA	161436
rs748731577	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88626262	ACAGAAATTTTAGGA[C/T]ATTTAGGGTGACAAT	161436
rs748732198	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88666840	CAGAATGAAAAGTTA[C/T]AGCATAAGTTGAGAA	161436
rs748737500	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764131	TATTATCCTACTGAC[A/G]GATTTTATTTGCTTA	161436
rs748747649	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780723	TGGGATTACAGGCGC[A/G]CGCCATCATGCCCAG	161436
rs748748462	snp	A/G	0.000231441	0.0107549	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620892	TAACACACAGTACGA[A/G]CAGCATGTCCCAAAT	161436
rs748752875	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88710925	ATAATATCGACTTCT[C/G]TCTTGCAAATGATAA	161436
rs748760809	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88630528	TTCAGGGGAAACAAA[-/C]TGCATGCTCAACTAA	161436
rs748807693	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88794734	TAAATTTTATGAGAC[A/G]AGATGGAAGAATATA	161436
rs748816180	snp	C/T	1.68655e-05	0.00290387	intron-variant	EML5	GRCh38.p7	14:88622731	GACCTAAGTAAATAA[C/T]CAAGCCAGAGTAAGT	161436
rs748820591	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88641347	CCATAGAAAACTACA[A/G]AACATCCCACACAAA	161436
rs748828628	snp	A/C	3.31312e-05	0.00406995	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736536	CTAGAATGTGGTCAC[A/C]TCGCCAACACACACT	161436
rs748846250	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88748144	AGAGGACAAGATGCC[G/T]AGAATTTGCAGAGCA	161436
rs748850440	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660492	TCACGCCTGTAATCC[C/T]AGTACTTTGGGAGGT	161436
rs748858906	snp	C/T	1.82201e-05	0.00301823	intron-variant	EML5	GRCh38.p7	14:88704994	CTTTAAAAATGTATA[C/T]AAGTAGAAATATTCT	161436
rs748859098	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711433	ATGGCAGAAGGTGAA[A/G]GGGAAGCAAGGCACC	161436
rs748866006	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88697673	ATATCTTTGTATATA[C/G]AGACAACTCCTGAAA	161436
rs748875600	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643625	TTTTTTGTGTCCAAA[A/G]GAAGAAAATTTTATG	161436
rs748914147	snp	C/T	0.000100128	0.0070749	intron-variant	EML5	GRCh38.p7	14:88736330	TATCTAAGGATACAT[C/T]CCAGCCTATGGAATT	161436
rs748946484	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88681501	TCTATTTACAATATC[C/T]TTCCTCAGCTGTCTA	161436
rs748955467	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88781300	TTCCAGTAGGGTAAA[A/T]CTGCAGAACTTTCAC	161436
rs748957304	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767947	TATCCAGGATCCCAT[G/T]CTGCATTTTAACTGT	161436
rs748964246	snp	A/G	3.36146e-05	0.00409953	intron-variant	EML5	GRCh38.p7	14:88644418	CAGTAACACTGGAGA[A/G]TGAGTTTTCCTTACC	161436
rs748982239	in-del	-/A	0.00784126	0.062122	intron-variant	EML5	GRCh38.p7	14:88687333	TACAAACCCCTATGG[-/A]AAAAAAAAAGGTTCA	161436
rs749016206	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88712963	GAGGACTTTAGGACC[C/T]GGTCAGTCTTCATTA	161436
rs749021847	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88702269	AAAATAATAAAAACT[C/G]TAAAACTGTAGGAAA	161436
rs749040223	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88686792	CTCCAGCCTGGGCAG[C/G]ACAGCAGGACCCTGT	161436
rs749040657	snp	A/C/G	6.63376e-05	0.00575891	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665446	ATCGTTGAGACCTAC[A/C/G]GCTAAAGCTTTACCA	161436
rs749044508	snp	C/T	1.76842e-05	0.00297352	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661830	AAGCAATTTTTTCTA[C/T]CTAAAAATGAAAAAC	161436
rs749049380	snp	C/T	1.66029e-05	0.00288117	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714998	TGCAAATATCTACTG[C/T]CTGAAGACCAGTCCA	161436
rs749053066	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88738709	TAAACTCTTTACAGG[A/C]AAAATTTCTCCTTAA	161436
rs749055531	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88785612	TTGTTCTGACCAAAA[A/G]TTCTGTGATCATCAC	161436
rs749057057	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88705365	GGGAAAACTAATATA[C/G]TCATACATTGCTTGA	161436
rs749065359	in-del	-/GCACCAGTTAGAA			intron-variant	EML5	GRCh38.p7	14:88728321	TGACCCTTGAATAAT[-/GCACCAGTTAGAA]GCACCAGTTAGAAGC	161436
rs749067130	snp	G/T	1.70165e-05	0.00291684	intron-variant	EML5	GRCh38.p7	14:88638781	GCAAATGCTTTAAAT[G/T]GTTTCTTTTTAAAAT	161436
rs749099717	snp	A/G	1.73339e-05	0.00294392	intron-variant	EML5	GRCh38.p7	14:88714906	AAATATTGTATAGGT[A/G]CTACAAATCTATAAT	161436
rs749116117	snp	G/T	1.77833e-05	0.00298183	intron-variant	EML5	GRCh38.p7	14:88740606	AATCAAATTACCAAA[G/T]AATTCTTATAAAATA	161436
rs749126474	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88635062	TATGAGTACAAGTTT[G/T]CCAAGAAAGAAAATG	161436
rs749141820	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633682	TACACACCTCTGCCA[C/T]TGTAGCACAAAAGCT	161436
rs749146316	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721565	AACTGGCCAGCTATA[C/T]GCGGAAAACTGAAAC	161436
rs749184716	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761452	GAGAACATGTGGTGT[C/T]TGGTTTTCTGTTCCT	161436
rs749191567	snp	C/T	1.76968e-05	0.00297457	intron-variant	EML5	GRCh38.p7	14:88618364	AATGGGACAAGAATT[C/T]CATTAGGTGAGAGAC	161436
rs749197669	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88709853	AAAAGGCATTAAAGC[G/T]ACACGCAACAATATG	161436
rs749221808	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88659393	TTTTTTCTGTTTTTA[A/C]TAGAGACGGGGTTTC	161436
rs749224547	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88728002	TGTTACTATTTTGAA[A/G]TAAGTTATAAAACTG	161436
rs749247476	in-del	-/AAAT	1.77674e-05	0.0029805	intron-variant	EML5	GRCh38.p7	14:88704832	AACCAAAATTCAAAC[-/AAAT]AAATGAAAGATAGTT	161436
rs749277313	snp	A/C	1.68661e-05	0.00290392	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618230	TATAAGTATTTACCT[A/C]GTCCATGTAGCCCAA	161436
rs749284260	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88674633	TCATTCTGACCCTGG[A/C]ACTTCCCAAATTTCA	161436
rs749306658	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88619671	AATGACACAACTTGA[A/T]TCTTGGAAGAAGAAT	161436
rs749320230	snp	C/G	6.63328e-05	0.00575865	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658232	CTTCACTATCACAAG[C/G]CCTTTTTTCTCGATA	161436
rs749322213	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88678146	GTCCTTTGTGGGGAC[A/T]TGATGGAGCTGGAAG	161436
rs749347796	snp	C/T	1.80781e-05	0.00300645	intron-variant	EML5	GRCh38.p7	14:88706451	AAATATATCTTTAAA[C/T]TGATAAACAAATGCT	161436
rs749351149	snp	C/T	1.87436e-05	0.00306128	intron-variant	EML5	GRCh38.p7	14:88740380	TAAAATACTTAAATG[C/T]ACTTACAGCATGGGC	161436
rs749357080	snp	C/G	3.31378e-05	0.00407036	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740473	CAGAATATGTTAATT[C/G]ATCCCTTGCACAGGC	161436
rs749360126	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784032	ACGTGGAAATTAAAC[A/G]ATATGCTCATGAATG	161436
rs749374443	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778877	TCCCTTTTAAGCATA[C/T]AACAGGATTTCATTT	161436
rs749375758	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88752093	TTCTCATGAAGATCT[C/T]TGATAATGAAATACA	161436
rs749378910	snp	C/T	1.65924e-05	0.00288027	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685112	CCTAATGATATGGCA[C/T]GTATAGATGGATTAT	161436
rs749379058	snp	C/T	2.33582e-05	0.00341739	intron-variant	EML5	GRCh38.p7	14:88657526	AAAATATACGAGTAA[C/T]TCTTTAAGCAATAAC	161436
rs749382859	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88744797	CATGTTTCTTTGACA[C/G]CTTATCAACCTACCT	161436
rs749439082	snp	C/T	6.63922e-05	0.00576123	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616254	TTGCCTAAAAAACAA[C/T]GACAGACAAGCTCAG	161436
rs749469861	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647301	CCCAGGAAACGGAGG[C/T]TGCAGTGAGCCAAGA	161436
rs749470122	in-del	-/CT	1.66222e-05	0.00288285	frameshift-variant, splice-acceptor-variant, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625109	CACCACTGATGGTAC[-/CT]GTAAACGTCAAGTTA	161436
rs749506331	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88715369	TTGCTGAACAGAAAT[A/G]CATGGAAACAATATA	161436
rs749531256	snp	C/T	3.57124e-05	0.00422551	intron-variant	EML5	GRCh38.p7	14:88704825	AAGTGTGAACCAAAA[C/T]TCAAACAAATAAATG	161436
rs749553915	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705468	GAGAAAAACCATGTG[A/G]TATGGAAAATTACCT	161436
rs749571395	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88648691	GAAGTGGCCTCCCAA[C/T]CTCCCTTCCTCCTGT	161436
rs749573118	snp	A/C	1.66888e-05	0.00288862	intron-variant	EML5	GRCh38.p7	14:88684989	TGTATGTAAAGAAAA[A/C]AAAACAAATTAGCAT	161436
rs749578989	snp	C/T	0.000168677	0.00918204	intron-variant	EML5	GRCh38.p7	14:88621904	CCTCTCTTGTAAATA[C/T]CTGAAAATACATAAA	161436
rs749585813	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784386	AAGTTAAACAAGATT[A/G]ACAAACCTTTAGCCA	161436
rs749601354	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719623	TATGTGTATATATAA[C/T]TTTCTACTTTAAAAT	161436
rs749623750	in-del	-/TTGTTTGTGTGTGTGG/TTGTTTGTGTGTGTGTGA			intron-variant	EML5	GRCh38.p7	14:88745170	AAATTGTGTGTTTGT[lengthTooLong]GTGTGTGTGTGTGTG	161436
rs749630352	snp	C/G	8.29456e-05	0.0064394	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616796	GTAACAAGACTGATT[C/G]CTGAATGAGATACAC	161436
rs749638640	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88757663	AAACAAATAAAGGAT[G/T]TTAACAGACATACCC	161436
rs749648892	snp	C/T	7.41537e-05	0.00608863	intron-variant	EML5	GRCh38.p7	14:88754714	TATTATTAAAAATTG[C/T]TTATACAGATTTTAT	161436
rs749689972	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88654325	TCTTCTACTAGCTTT[C/T]GAATTTGTTTGCTCT	161436
rs749691579	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88743904	ACAATAAAAACATTG[C/T]CATTTTAAAAATAAG	161436
rs749702040	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88759157	GTTATGTGAATCATA[C/T]CTCAGTTTTTAAAAA	161436
rs749702566	snp	C/T	9.4802e-05	0.00688419	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695442	CCAACTGATGCCAAA[C/T]GTTTCCCATCCGCTG	161436
rs749740330	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88655549	ACCTAGCTAATACCA[A/T]TCAGGACTTGGCATG	161436
rs749747754	snp	C/T	3.86623e-05	0.00439655	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627744	ACTGAACATACTCCC[C/T]TTGAATGGTAGCATC	161436
rs749749650	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88638422	CCCACGGAAGCAGGG[C/T]TCTACCCCGCCCAGT	161436
rs749752202	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88693548	TACAAGTGAAGGTGA[C/G]ATTTGGGTGGGGACA	161436
rs749755534	snp	C/T	1.66463e-05	0.00288494	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712359	ATAATTTCCATCTAC[C/T]GAATTTATATCGTTG	161436
rs749762832	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88790218	TAAATTTGTGCCACC[A/T]ATTTCAAGATGCTGT	161436
rs749777137	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88692287	GAGGCTGAGGCAGGA[C/G]AATCACTTGAACCCA	161436
rs749810736	in-del	-/GGA			intron-variant	EML5	GRCh38.p7	14:88664183	CAGGAGGCTGAGTTG[-/GGA]GGAGGATGACTTAAG	161436
rs749827619	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88745544	AATGTAATAGTAATA[C/T]GTAATTTTAAATCCA	161436
rs749834700	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755801	AGTTCAAGATCACCC[C/T]GGGAAACACAGCAAA	161436
rs749864048	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639770	ATTTTTAGTAGATAC[A/G]GGGTTTTGCTGTGTT	161436
rs749866569	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623830	TGCAGGAGTAAATGA[C/T]GTGGGAAATACAAGT	161436
rs749868900	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88739833	AAGAAAAGGGTAGGA[A/G]AACCCAATTAATAGA	161436
rs749870664	snp	C/G	1.66724e-05	0.0028872	intron-variant	EML5	GRCh38.p7	14:88627074	AACAAAATTATCTAG[C/G]TTATTACAAGAACCA	161436
rs749900135	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88786579	GTCCCCACCCAAATC[A/T]CATCTCGAATTGTAC	161436
rs749900775	snp	C/T	3.4915e-05	0.00417807	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621113	ATTATCTGTACTTAC[C/T]TTATCAGCAATATCC	161436
rs749901278	snp	C/T	1.6888e-05	0.00290581	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696928	TCTCTGTATCCCATA[C/T]ATGAATTGAGGGATC	161436
rs749909241	in-del	-/G	1.66907e-05	0.00288879	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88618246	GTCCATGTAGCCCAA[-/G]TAATTCTGTCAATAG	161436
rs749912512	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88688896	AGTATTGTGAATGTG[A/G]TACTGATTATTCTCA	161436
rs749912657	snp	A/T	2.07063e-05	0.00321756	intron-variant	EML5	GRCh38.p7	14:88696809	ATGTGTTGCCTCTGC[A/T]TTTTGTTAATTCTTA	161436
rs749912684	in-del	-/A	4.79921e-05	0.00489834	intron-variant	EML5	GRCh38.p7	14:88621092	GTTGTAACCTCTTTT[-/A]AAAAAATTATCTGTA	161436
rs749921616	snp	C/G	0.000149466	0.00864352	missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792379	TACACCACGCCGACC[C/G]CCGCCACGAAGTATA	161436
rs749925238	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88634877	ATAACTCAAGAAAGG[A/T]AACAAGTTCTTTCTT	161436
rs749928664	snp	G/T	3.5163e-05	0.00419288	intron-variant	EML5	GRCh38.p7	14:88754701	AATAAATAAGTAGTA[G/T]TATTAAAAATTGCTT	161436
rs749955590	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88722557	TTTATAAGTGGGAGC[C/T]GAACAATGAGAACTA	161436
rs749999383	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88787441	TTTCCTTAATGTATA[A/T]CCAAAACATGTTTTA	161436
rs750018615	in-del	-/TCTA			intron-variant	EML5	GRCh38.p7	14:88706519	CCACTGTATCATCCT[-/TCTA]TCTGAATTATAAACA	161436
rs750023425	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88641555	TTTACCATATAAACA[G/T]AATTAAAAACAAAAA	161436
rs750029021	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88737778	TTCTTCCTTCTCCCT[C/T]GTAGACAACTCTAGC	161436
rs750038951	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674488	AAACCATCAGATGTC[A/G]TGAGACTCACTATCA	161436
rs750044605	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88723854	GATAAGTTTTAAGAA[A/G]ATATTGTGGCTTTAC	161436
rs750051866	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88619482	GGTACTGGGATTACA[C/G]GTGTGAGCCACAACA	161436
rs750066524	snp	C/G	3.78279e-05	0.00434885	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620857	TCATTCCAATAGCCA[C/G]CATGTCCCCTTCAGG	161436
rs750079792	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88765186	TCCCAGTTCTGCAGG[A/G]CAGAAATCTGGTTAG	161436
rs750082618	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671544	AGGATCAAATTCACA[C/T]ATAACAATATTAACC	161436
rs750124247	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715823	GCACACCACCATACC[C/T]GGCTAATCTTTTTGA	161436
rs750133885	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88668777	TAGTAAGTATCCTTT[-/A]AAATTCATAGCTGAG	161436
rs750135732	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88775201	CAACTGTGGTGGCCA[C/T]GGGGCGAAACTCCTT	161436
rs750138396	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88675716	GATATTCTTTTCTGT[C/G]ACAGTCAGGCTGCAA	161436
rs750140920	snp	C/T	1.65866e-05	0.00287976	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625070	CGATTCTACACAATA[C/T]GTGATCTTTCCACAC	161436
rs750144508	snp	A/G	1.70542e-05	0.00292007	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627687	GTATGTTCTGGGTCT[A/G]GTCCCACAGACAGCA	161436
rs750190162	snp	C/T	3.53232e-05	0.00420242	intron-variant	EML5	GRCh38.p7	14:88738848	GAAGTTTAGAGTTTG[C/T]CTAGTAATAAGACAT	161436
rs750192898	snp	A/T	7.42914e-05	0.00609428	intron-variant	EML5	GRCh38.p7	14:88705613	TTAAAAATGAAATGT[A/T]ACTTGTTTAAAGAAG	161436
rs750194821	snp	C/T	1.65792e-05	0.00287912	intron-variant	EML5	GRCh38.p7	14:88688259	AATTTAAAATCTCTT[C/T]AGGTTACTTACTTTT	161436
rs750233847	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779685	TCAAGATATTCTAGG[C/T]GCAAACCAGGATCAG	161436
rs750244885	in-del	-/AAGTTA			intron-variant	EML5	GRCh38.p7	14:88659072	ATAACAATAAAGTTT[-/AAGTTA]TTGTTATTATGGTAT	161436
rs750246271	snp	C/T	3.29018e-05	0.00405584	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705518	TGTCTCTTGTTCAAT[C/T]TCAGAATCCAGTTCT	161436
rs750254096	snp	A/C			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715120	TCCAACAGCAAGGTA[A/C]GTTCCATCTGGTGAA	161436
rs750256046	in-del	-/ACTT			intron-variant	EML5	GRCh38.p7	14:88691845	CTCACCAAAGCCTTA[-/ACTT]ACATTCATCCTTTTA	161436
rs750307827	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88667738	CTGGCATGAAGGGGG[C/G]CTGATGGCATTCACC	161436
rs750327276	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88716573	TAAAATTTTATAATT[A/G]TAATCTTCATGACCT	161436
rs750332328	snp	C/G			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626714	ATGAAATATATGCTT[C/G]ACCAGGGCATGTAAT	161436
rs750350079	snp	A/C	1.70043e-05	0.0029158	intron-variant	EML5	GRCh38.p7	14:88646962	CTGGAACCTCTTTTC[A/C]GCAGCAGATAAAGAG	161436
rs750357624	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88689744	GTCTCCAAACAAAAA[C/G]AGAGAGAGAGAAAGA	161436
rs750372665	snp	G/T	4.87948e-05	0.00493913	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615889	TTGCAGGGAGTTAAT[G/T]ATGTTTTTAGATTTT	161436
rs750377063	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88702065	AAAATAAAGAGACAT[A/T]GTCCTTTGGTTTGTC	161436
rs750397286	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644692	GAAGGTAGAAAGAAA[A/G]TATTACAACTTTTAT	161436
rs750403091	snp	C/T	0.000163063	0.009028	intron-variant	EML5	GRCh38.p7	14:88681849	TAAAGGTTAGAAAAC[C/T]GTGAGAGCTTAATCT	161436
rs750406872	snp	A/G	1.65913e-05	0.00288017	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644493	CTCTGGCTGTGGTGG[A/G]GCCCTGCTCACTGGA	161436
rs750433846	in-del	-/TC			intron-variant	EML5	GRCh38.p7	14:88683552	AACTAAATACCAATA[-/TC]TCTTATAAATACTGA	161436
rs750434858	snp	G/T	1.65627e-05	0.00287769	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736524	CCTGTGTTCCAACTA[G/T]AATGTGGTCACCTCG	161436
rs750435005	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88706768	CAACTAGACCTTACC[A/C]CCATTATTCTCAACC	161436
rs750443858	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88759019	AGAATGGATAAGGAC[G/T]GCTAATGAGCTTGGG	161436
rs750447404	snp	C/T	0.000152033	0.00871743	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726602	GATGGATTCCATCTG[C/T]ATTGACAGCTGCACA	161436
rs750452217	snp	A/G	2.04397e-05	0.00319678	intron-variant	EML5	GRCh38.p7	14:88702669	ATATAATTAATTTTG[A/G]CCTTTTATCTGATCA	161436
rs750463022	snp	C/G	1.68224e-05	0.00290016	intron-variant	EML5	GRCh38.p7	14:88643043	ATGATAATAATAAAA[C/G]CATTATATTCTTCCT	161436
rs750466589	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88771244	AGCACAGTTCCCCCC[-/T]ATCAACCTCTGCCTT	161436
rs750478520	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720881	TCTAGAAAACTCCAT[C/T]GTCTCAGCCCAAAAG	161436
rs750501290	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617719	TGATCCTCCCACCTC[A/G]GCCTGCTACATCAGA	161436
rs750506642	in-del	-/ATG	5.03935e-05	0.00501938	intron-variant	EML5	GRCh38.p7	14:88685155	GACCTGAAATGTTAA[-/ATG]AAGATGTTCTTTTAG	161436
rs750521418	snp	A/C	6.65868e-05	0.00576966	intron-variant	EML5	GRCh38.p7	14:88726499	TTATATTCTGTATCA[A/C]TGAAGATAAAATTAT	161436
rs750558993	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88672864	ATCCCTGAATAGACC[A/C]ATAACAGTTCTGAAA	161436
rs750559131	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88655480	CAAAAATTAACTCAA[A/G]GTGAATTAAAGACTT	161436
rs750568015	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760299	CATTTAAAGCTACAA[C/T]CTATTTTGAGTTAAT	161436
rs750611863	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88657892	ATATTACTGGTATAT[C/T]AGAAGAAAATCAAAA	161436
rs750618793	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778753	CACTGCACTCCAGCC[C/T]GGCGACACAGCAAGA	161436
rs750626127	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88791092	CAATTTTGTCTTTTC[G/T]TATCTTTACTCCATC	161436
rs750647201	snp	A/C/T	0.000255239	0.0112945	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618803	CAGATACCGGGAATC[A/C/T]GGACTAAATCTGAAT	161436
rs750653808	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701810	ACCTAAACCTCATCA[C/T]TTGTAGACTGAAGGA	161436
rs750661186	snp	G/T	1.66588e-05	0.00288602	intron-variant	EML5	GRCh38.p7	14:88664633	CCAGAACCTATAATA[G/T]AAACATATTTGCTTG	161436
rs750663354	snp	A/G	3.32082e-05	0.00407468	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642954	TATATCATCACCATC[A/G]TTTAAATAGTGAACA	161436
rs750679355	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793656	AGGCCTCCCAAAGCG[C/T]TGGGATTACAGGCCC	161436
rs750681142	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88640554	CATGTAGCAAAAGCA[C/T]GTTAAATGTTAAGAG	161436
rs750697167	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88638394	GGGTCCTCTCTTCTT[-/T]CCAGCCTGAACCCCC	161436
rs750700659	in-del	-/T	2.09247e-05	0.00323448	intron-variant	EML5	GRCh38.p7	14:88696804	ATGCTATGTGTTGCC[-/T]CTGCATTTTGTTAAT	161436
rs750718468	snp	C/T	0.000116911	0.00764473	intron-variant	EML5	GRCh38.p7	14:88663160	TACACATATAAAATA[C/T]ATACAAATATATATA	161436
rs750743713	in-del	-/TAATT			intron-variant	EML5	GRCh38.p7	14:88719619	CCATATGTGTATATA[-/TAATT]TAATTTTCTACTTTA	161436
rs750749100	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88751090	AATAACAAACTAGAC[C/T]TGAGAGTACTTTCTC	161436
rs750756311	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88698887	CCTTACGAACATTGA[C/G]TCATGTACCAATCAC	161436
rs750762273	snp	C/T	1.65723e-05	0.00287852	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658281	CCACACCATTAAAGA[C/T]ATATCTGTACCGCCT	161436
rs750764798	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88700131	GTATTTGCTGAATTA[A/C]ACAAAATTTCCAAAT	161436
rs750770758	snp	G/T	4.97723e-05	0.00498835	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658216	GAATCAATGTCGGAT[G/T]CTTCACTATCACAAG	161436
rs750776675	snp	C/T	1.66413e-05	0.0028845	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712345	AAAACTTGGCCAATA[C/T]AATTTCCATCTACTG	161436
rs750795896	snp	A/G	1.68641e-05	0.00290375	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740558	GGTCAGAGCATTTCC[A/G]CATAAACTCCAGAAC	161436
rs750800837	snp	C/T	2.41391e-05	0.00347404	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687232	TTTAGATCCTGGGGC[C/T]AATGCAGCTCTTTTT	161436
rs750800864	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88782223	TTACTATGCAAAGAG[A/T]CTGGCAGCATTTTGC	161436
rs750801827	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783379	GATGAACAGATCAAT[A/G]GAAGATCCAATGGAA	161436
rs750847929	snp	A/G	1.66388e-05	0.00288429	intron-variant	EML5	GRCh38.p7	14:88616917	AACTCATCATGGCAA[A/G]TGCGGGCAGGTTGAC	161436
rs750857798	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652062	TCTGACTCCAGAATT[C/T]ATGTCCTTTGCACTA	161436
rs750875379	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88719560	TGGGTGCCTCTGAGG[A/G]GTTTGCTGTTGATAA	161436
rs750878102	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88630905	CGGAAAGTCCCTGGG[A/T]TCTGGATGACATCAT	161436
rs750881913	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88626077	TTCTTCCCTCGAAGT[-/AG]AGACACTGGCCCAGA	161436
rs750889441	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88685822	GTAAATAGCTGTTAT[A/T]CTGTATTTTTAATTT	161436
rs750889645	snp	A/G	1.65773e-05	0.00287895	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616808	ATTCCTGAATGAGAT[A/G]CACAGGCACAGTTGA	161436
rs750897466	snp	A/C/T	9.96755e-05	0.007059	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616175	GCACTAACAACATGT[A/C/T]GATCACCACTGGTAA	161436
rs750921935	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88680065	TCATTTTATGAAGTA[C/T]TTACTTTTAATAATT	161436
rs750926434	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88677950	TACTGAGTATATACA[C/G]AAAGGAACAGAAATC	161436
rs750929568	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88632708	AGAACTTCTGAAGTG[A/T]TCTCCATGTTGACAA	161436
rs750938617	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88746999	TGGCTGTGTCTTCAA[A/G]CAACTTCAACAATGT	161436
rs750966241	snp	C/T	1.65811e-05	0.00287929	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685094	ACTAAAATATGACCA[C/T]GTCCTAATGATATGG	161436
rs750989457	snp	A/G	7.2619e-05	0.0060253	intron-variant	EML5	GRCh38.p7	14:88618834	CAAAACAAAACGTAA[A/G]AAGTATTAGACCACA	161436
rs750996207	snp	G/T	1.66208e-05	0.00288273	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88704906	CTGGAGCCCGCTCTC[G/T]TCTTTTAGAAGTAGC	161436
rs750999757	in-del	-/TTAAA	8.11524e-05	0.00636943	intron-variant	EML5	GRCh38.p7	14:88638775	AACAAAGCAAATGCT[-/TTAAA]TTGTTTCTTTTTAAA	161436
rs751011723	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671868	TATCCTAAATATACA[C/T]GCACCCAGTTCAGGA	161436
rs751016817	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767101	ATAAACTCTGAATCC[G/T]CTTAAAATTTTCCAG	161436
rs751017368	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764913	TTTGTTAAGGTTTGT[C/T]TTATAATATATAGCC	161436
rs751028685	snp	C/G	1.66796e-05	0.00288782	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712386	GTTGATATCTGAATA[C/G]TTGGGCCAAATTCCA	161436
rs751040989	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700529	AAGGAATTCTTCCAA[C/T]GACTTAACTTTATCT	161436
rs751047423	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88701806	CCAAACCTAAACCTC[A/C]TCATTTGTAGACTGA	161436
rs751082769	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88648147	AGGAATCATGAAAGT[A/C]ATTTCATCCATTTTC	161436
rs751098754	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88737674	TTGATCTATACTCAC[A/G]TTTTCTTCAATTGTC	161436
rs751122996	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88633354	TGAACTCCTGGCCTC[A/G]GAACTCCTGTCTCAG	161436
rs751132338	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88754346	CTTGACATGATGAAA[A/T]AAAAACCCCATTGTT	161436
rs751146842	in-del	-/TTCA	1.6998e-05	0.00291525	intron-variant	EML5	GRCh38.p7	14:88658428	ATCTTTCTGAGAAAT[-/TTCA]TTATTTAAATATTTC	161436
rs751198977	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88649746	CAACCATATATGCTA[C/T]CTAAAAATGCAACTC	161436
rs751203420	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88785047	ATTTGCAACATCATG[G/T]ATGGGACTGGAGATT	161436
rs751214191	snp	G/T	1.65855e-05	0.00287967	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616798	AACAAGACTGATTCC[G/T]GAATGAGATACACAG	161436
rs751225574	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88696026	GGCTGTAAAGGCTCA[A/G]ACCACAAGAAAATAT	161436
rs751233196	snp	A/G	1.66768e-05	0.00288758	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740421	GTTCGTATAAGATTG[A/G]TTCCTTTCCAAACAT	161436
rs751258383	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786335	ATAAAATTTACCTTC[C/T]TTATTCTGTGTCTCC	161436
rs751264959	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88688609	AGAATTGAAAACTAC[A/G]GGTGTCTCAATCAGT	161436
rs751282565	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639285	TCTAGACAGAGGAAC[A/G]CTTTAAGCAGAGGCC	161436
rs751295931	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88713445	CTGCTTTTATTCCAT[A/C]CATTCATGCACTCAC	161436
rs751303329	snp	A/G	1.65976e-05	0.00288072	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658209	TTCTTCAGAATCAAT[A/G]TCGGATTCTTCACTA	161436
rs751345650	snp	C/T	9.6214e-05	0.00693525	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792366	CTCCCGCGGGCTGTA[C/T]ACCACGCCGACCCCC	161436
rs751381199	snp	G/T	1.66449e-05	0.00288482	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704947	TTCTCTTTGCACTGT[G/T]CTTTAAGCTGAGGTA	161436
rs751416893	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778562	GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGATCC	161436
rs751427954	snp	C/T	5.09334e-05	0.00504619	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726642	TTCTTCCATATTACA[C/T]CTTGCTATTAATGCA	161436
rs751450923	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88624238	TGTGCCACCACACCC[A/G]GCTAATTGTTGTTTT	161436
rs751453566	snp	A/G	1.69781e-05	0.00291355	intron-variant	EML5	GRCh38.p7	14:88754691	AAAATAAGGAAATAA[A/G]TAAGTAGTATTATTA	161436
rs751456917	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727919	AGAAGATACCCATTG[C/T]TTGAAAATTAAGAAT	161436
rs751467551	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711822	TGGTGGCACATGCCT[A/G]TAATCCCAGTTACCT	161436
rs751482019	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88713795	GTTGCAATTCTGTTT[A/T]TCAAAGTTAGTTAGT	161436
rs751511724	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88729638	AATCTTAGTTCACTG[C/T]AACCTCCGCCTCCCA	161436
rs751521052	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88638018	CGCATGAAAAATAAA[C/G]ATATTAAAAGTATAA	161436
rs751523674	snp	C/T	0.000277739	0.011781	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88663115	GTTGACCTGTAAAAG[C/T]TTTCCTTCAAAAAAA	161436
rs751524824	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766488	ATAGCGCTCCCAGGC[G/T]TATTGGGACGAGGAA	161436
rs751534803	snp	A/G	2.10038e-05	0.00324059	intron-variant	EML5	GRCh38.p7	14:88696798	ATTAAAATGCTATGT[A/G]TTGCCTCTGCATTTT	161436
rs751536040	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88727432	TTGAGACGGAGTTTC[A/G]TTCCTGTTGTCCAGG	161436
rs751537160	snp	C/T	3.3428e-05	0.00408814	intron-variant	EML5	GRCh38.p7	14:88664659	GCTTGACATTTTCTA[C/T]CTTTGGAAATACTTT	161436
rs751573363	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614988	AGACTACATTAAATA[C/T]GCAATTCTTTCTTCC	161436
rs751587108	snp	C/T	6.23383e-05	0.00558259	intron-variant	EML5	GRCh38.p7	14:88638921	ACCTACAAAAAAGAA[C/T]TTGAGAATTAAGTTT	161436
rs751596718	in-del	-/AATTA	2.97221e-05	0.00385489	intron-variant	EML5	GRCh38.p7	14:88696984	GAAGCTATTAAATAC[-/AATTA]AATTATTTATTTCCA	161436
rs751596941	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717655	AGCTACTCAGGAGGC[C/T]GAGGCAGGAAAATCA	161436
rs751606428	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666161	ATGTGGAAGTTTTGC[A/G]GAGTAGGTTTTACCT	161436
rs751617685	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735871	TTTGTACATTCTGAT[A/G]TGGAACAAACTCCAT	161436
rs751634695	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88771400	TCCTTGAACTCTCCG[A/C]TTGTGTTCTAGGTCC	161436
rs751640245	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630708	CAGGCTAAAATGACT[C/T]AGTCAGGCTAAACGG	161436
rs751645859	in-del	-/AA	2.40012e-05	0.00346411	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88739003	ACAAGCATTCATGCT[-/AA]AAATTCCTGCCTAGA	161436
rs751647882	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719449	CTATCCCATACCCTG[C/T]GGGAAACCTTACTCC	161436
rs751697215	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757146	TCAATCAAACAGAAT[C/T]GTGAGTCCAGAAGTA	161436
rs751710566	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88670921	AGAACTATGGGATTA[C/T]GTAGAAAGACTGAAC	161436
rs751727403	snp	C/G	1.67396e-05	0.00289301	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88744068	TTTATTTGGCTGGTA[C/G]AAATCCCAAGAAATA	161436
rs751734448	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88656175	ATGCACATGTATATT[G/T]ATTACAGCACTGTTC	161436
rs751757897	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88628670	TGTTTTAAAAATAGA[C/G]AAACATTAAGACAAG	161436
rs751771621	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691363	TACCTACATAATACC[C/T]TTGATTTTGTCCTTT	161436
rs751772705	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88706706	TTAAAACATTTGAAT[A/G]TTTTGGCCTGAGGCC	161436
rs751785178	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88658618	CTGGTACCCCAGGCA[A/G]AACTCTTTAAAAAAC	161436
rs751789187	snp	A/G	1.71634e-05	0.0029294	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661816	TGTCCATGATGCCCA[A/G]GCAATTTTTTCTACC	161436
rs751790893	snp	A/G	1.88681e-05	0.00307143	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626802	AGAGAATGTAAAGTA[A/G]TCAAAGTCACACTAT	161436
rs751797561	snp	C/T	2.03461e-05	0.00318946	intron-variant	EML5	GRCh38.p7	14:88618631	CTTGCCACCTGGGTA[C/T]ACAGTATTGGTACTG	161436
rs751816724	snp	A/G	0.000132994	0.00815349	intron-variant	EML5	GRCh38.p7	14:88688515	TACCACTTTCAAAAT[A/G]TACTCAATTATAAAG	161436
rs751825475	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88708009	TAAAGAGTTATCTCA[A/G]CATCTGATCTGCCTA	161436
rs751849864	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88743223	CACTGTAGAATGAGT[A/G]TAGGTAATATGAATA	161436
rs751867100	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638004	ATCAACTTAGTACTC[A/G]CATGAAAAATAAAGA	161436
rs751869732	snp	A/G	1.65611e-05	0.00287755	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688404	TCAGTCCATCCATAC[A/G]CTGCACACATCATTG	161436
rs751870270	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712164	CCTTCACCAATCAGT[A/G]TAATTTTAAAAAATA	161436
rs751870520	snp	A/G	1.65965e-05	0.00288062	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616223	TGGGGCGAATGACCC[A/G]AGAACCTTTTGTGTT	161436
rs751882568	snp	A/G	1.68502e-05	0.00290255	intron-variant	EML5	GRCh38.p7	14:88684968	TTATATATTGAAATA[A/G]TCAATTGTATGTAAA	161436
rs751904462	in-del	-/ATAAGT			intron-variant	EML5	GRCh38.p7	14:88703188	TATACTACCATTTAC[-/ATAAGT]ATAATATTAAAATTG	161436
rs751907993	snp	C/T	1.6574e-05	0.00287867	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685065	CTTCTAGTATTTCAC[C/T]ATTCTTTGTGCCAAC	161436
rs751910347	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88743850	CCTTACAATAGTTCA[A/C]AGCAAATAATATATA	161436
rs751912445	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88763464	AACCAGGAAGAAGTC[A/G]AATCCCTGAATAGAC	161436
rs751926121	snp	A/G	0.000239206	0.0109337	intron-variant	EML5	GRCh38.p7	14:88740354	GGTTAAGTAATACAC[A/G]TGAAAGTGTTTAAAA	161436
rs751931547	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88749557	TTAACAACTATTTAC[A/G]GCAAAATAACAGTTA	161436
rs751950476	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88662101	GTGTTAATAATAAAA[A/C]CGTTTCTGACTTTAG	161436
rs751967036	snp	C/T	0.000282905	0.01189	intron-variant	EML5	GRCh38.p7	14:88702639	CCTCTGTAACTAATA[C/T]AGAAAACAAATCATA	161436
rs752007584	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644812	GCCTCCTGGATTCAA[A/G]CGATTCTCCTGCCTC	161436
rs752009204	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698743	CCAAGTCCTTCTCTC[A/G]AGCAGTTACTTTTCC	161436
rs752011222	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88781128	TTAGGCTCCTCTATA[C/T]CACCCTGTGGGTTTA	161436
rs752061114	snp	C/T	3.6733e-05	0.00428546	intron-variant	EML5	GRCh38.p7	14:88621408	AGAGAACTTTTTGCT[C/T]TGAGCTAATCTAGTA	161436
rs752061753	in-del	-/AAC			intron-variant	EML5	GRCh38.p7	14:88726158	AAGGCTGTAAATAAC[-/AAC]AACAACAACAACAAC	161436
rs752068592	snp	C/G	3.35115e-05	0.00409324	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702487	AAGGATGAATAGTTA[C/G]GCAGAGAATATCATC	161436
rs752072716	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88629840	TGCTCTTTTCCCCAC[A/G]TGTAGCTCCCTCCAG	161436
rs752083068	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88750750	CCATCAAATCAAGCT[A/G]GCAGAAAGCCCAGAG	161436
rs752128920	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88646034	TGAATAACCGGAACA[C/T]TGAATTTAAATCAAT	161436
rs752129227	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88630754	TGGCTCTGAAAAGGA[-/T]TTTTTTTGCTTCTTT	161436
rs752133412	in-del	-/TTTG			intron-variant	EML5	GRCh38.p7	14:88624073	TATGTCACATTTTTT[-/TTTG]TTTTTGTTTTTGTTT	161436
rs752136969	in-del	-/AAAC			intron-variant	EML5	GRCh38.p7	14:88728865	AACTACATTATAAAT[-/AAAC]AAAGGCTACAATTTA	161436
rs752164769	in-del	-/C	1.65754e-05	0.00287879	intron-variant	EML5	GRCh38.p7	14:88621310	TCTTGCCCTGAAACA[-/C]AAGCAGGACCAATAC	161436
rs752183803	snp	C/T	3.57833e-05	0.0042297	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706375	TAATCATGTGACCAT[C/T]TGACATTAGTTACGT	161436
rs752188327	snp	A/G	4.99804e-05	0.00499877	intron-variant	EML5	GRCh38.p7	14:88658180	CAAGTATTATAAAAT[A/G]ACGTACCCCCATCTT	161436
rs752191025	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88751335	GAAGAGAGAGTCAGA[C/G]ACAGTTTGTAGAAAA	161436
rs752212196	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712645	TGGGTTAAGAGAAAA[A/G]AAAACTAAATGCAAG	161436
rs752216819	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88785305	TCAGTAATAATTTAA[G/T]TGTACATTTTAGAAT	161436
rs752230085	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88646776	TATACAGAGTAAGTC[C/T]AATAATTAAGATGTT	161436
rs752286293	snp	C/T	1.68233e-05	0.00290023	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738880	TGTTTTGTTATTACC[C/T]TTGTATCCCTGGTCT	161436
rs752288757	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88664426	GAATCACTTTTCCGT[G/T]TCTCTAATATAGCTA	161436
rs752308025	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692675	TGTAGTATATGCTGC[A/G]AATTTGCAATTACAA	161436
rs752333031	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88700329	TTTTATTTGGGAAAA[C/G]TGCTTCTTACAAAAG	161436
rs752353730	snp	A/G	1.79226e-05	0.00299349	intron-variant	EML5	GRCh38.p7	14:88621398	ACCTGCTTTCAGAGA[A/G]CTTTTTGCTTTGAGC	161436
rs752354768	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88631239	TTCTTTTTGAGACAA[A/G]GTCTCACTCTGTCAT	161436
rs752388204	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88701372	TATAGATCAGAGAAG[C/G]TTCTCTGCTCTATAC	161436
rs752395515	snp	C/T	1.67019e-05	0.00288975	intron-variant	EML5	GRCh38.p7	14:88664655	ATTTGCTTGACATTT[C/T]CTATCTTTGGAAATA	161436
rs752399846	snp	C/T	1.66554e-05	0.00288573	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616107	TCTTAACTAGTAACA[C/T]AGTCTGCTCTTCATG	161436
rs752400184	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88783576	AAGTGACAAAGTCAC[C/T]GTATAATGACAAAGG	161436
rs752421304	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88736353	ATGGAATTAGTTTAT[A/T]ATTTGCTTACCTGAC	161436
rs752423456	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88717131	AGACATATCAAAGGA[A/C]GTGGAGTAGATAGCT	161436
rs752425340	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88746403	CATAAAACATATATG[C/T]CTATATTTTATAGAC	161436
rs752425714	snp	A/G			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626862	TGCAATAGCGAGCAT[A/G]GTCTGCATCCGGGCA	161436
rs752435795	snp	C/T	1.73189e-05	0.00294264	intron-variant	EML5	GRCh38.p7	14:88682055	AAAACATAGGATCAA[C/T]TTAGTGTATGTGTGT	161436
rs752450801	in-del	-/TAACT	5.24224e-05	0.00511942	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88616753	ACATGGGAAGTCAAA[-/TAACT]TAACCATGCCAAAGT	161436
rs752463426	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647657	GATCACATCACTGCA[C/T]TCAGCCTAGGTAACA	161436
rs752485100	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756760	GAATAAAACATTTAG[A/G]AATAAATTAAACAAA	161436
rs752509167	snp	A/G	2.06349e-05	0.00321202	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88754652	TTGCTACCAACACTC[A/G]TTCAGGATGCAATGC	161436
rs752527286	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637131	CAAAACAATTCTCTT[C/T]ATGTGTGAGGAGAAA	161436
rs752540824	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706107	CTAACTTTAAACATA[C/T]AGAACTAATATTTTA	161436
rs752551062	snp	C/T	1.70863e-05	0.00292281	intron-variant	EML5	GRCh38.p7	14:88664481	CAAGTATTAAGTTAT[C/T]TAAAGTCTTACCTCT	161436
rs752578437	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88788537	CCCTTTCACTATGTT[A/T]AAAAAAAAAAAAAGT	161436
rs752580390	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88637544	ATATTCTAGAATTCT[A/G]TTTGCAGAACGTAAA	161436
rs752580426	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88775601	ATCCACAGTACAACA[C/G]AACACCAGGTAGACT	161436
rs752635406	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88639147	CCAAGTGCCACAAGA[C/G]AGTTGGGATCAAAAT	161436
rs752652462	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678430	CCTGCACATGTATCC[C/T]GGAACTTAAAATAAC	161436
rs752655014	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88754105	CACTCCAGCCTGGGC[A/G]GCAGAGCGTGACCCT	161436
rs752657786	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88726120	CTCAAACAAAAGAAG[A/G]GATGGAAGCATTTTT	161436
rs752675528	snp	C/T	1.65611e-05	0.00287755	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688354	CTCTCCAGATACACA[C/T]ATCTCCTGTGGATGT	161436
rs752675923	snp	C/T	6.66911e-05	0.00577418	intron-variant	EML5	GRCh38.p7	14:88618829	TGAATCAAAACAAAA[C/T]GTAAAAAGTATTAGA	161436
rs752675966	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691269	GCCAGACCCATTCCC[C/T]GGCAGACAGAATGTC	161436
rs752684047	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623091	CATGATCTAGGCTTA[C/T]TGCAACCTCTGCCTC	161436
rs752684139	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665618	GACTGCCCGCGGCCA[A/G]GAGGTTAAGACCAGC	161436
rs752694456	snp	A/G	1.65622e-05	0.00287764	missense, stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88626962	TGTTTTACTCCCACT[A/G]AGACAAACTGGGTAT	161436
rs752734339	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88677245	TGGGAAAACTGGCTG[G/T]CCACATGCAGAAAAT	161436
rs752753403	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88749196	GCCAGACAAAAAAGG[A/T]CAACTGCTGTATGGA	161436
rs752780257	snp	A/T	1.94414e-05	0.00311775	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88661663	ACATACTTTAGTAGG[A/T]TATCTAAATAACTTC	161436
rs752790622	snp	C/T	3.34191e-05	0.0040876	intron-variant	EML5	GRCh38.p7	14:88644526	CCTGCAACAGAGAAG[C/T]GGGGAGGAGGAAAGG	161436
rs752798301	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88683407	CAATAGAGCAATATG[C/T]TACCAATTAAAGGAG	161436
rs752816981	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780877	TGCACCTGGCTGAGT[A/G]GGGCCCCTTATAAAG	161436
rs752833137	snp	C/T	1.6638e-05	0.00288422	intron-variant	EML5	GRCh38.p7	14:88688239	CTCCAGGACAAATTT[C/T]GTTTAATTTAAAATC	161436
rs752845488	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88682335	AATAATTGCCACACA[A/G]GAGGTACTTTCCTGC	161436
rs752851088	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88779770	AGTCTGGGACTTGCT[A/G]TCTATACTGGCTTTG	161436
rs752877345	snp	A/C	1.675e-05	0.00289391	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618308	CACTTCATAGACATG[A/C]CGTTTATAGCAGCCA	161436
rs752877992	snp	G/T	1.71973e-05	0.0029323	intron-variant	EML5	GRCh38.p7	14:88624945	ACAAATGCATAAATA[G/T]TCTGTGAAAAGAAAG	161436
rs752884338	snp	A/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740468	TGCACCAGAATATGT[A/T]AATTCATCCCTTGCA	161436
rs752884824	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717628	GGTGTGGTGGCATCC[A/G]CCTGTAATCCCAGCT	161436
rs752891944	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770079	GCAGAGGAGAGGAAA[A/G]AGCGCTTGTGAAACG	161436
rs752893537	in-del	-/TATGAT			intron-variant	EML5	GRCh38.p7	14:88695209	TCTGAAATCATTTAC[-/TATGAT]TATGATTATATTATT	161436
rs752901004	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88669091	CAAGGGGAGCTCCTA[C/T]TCCCAGCCAAGAGAG	161436
rs752920129	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88629455	AGACTGTTCTAAACT[G/T]ACATCAGTAACAGTA	161436
rs752920623	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88670564	GAACTGGGCAAAGGC[C/T]GAGATGGATGAATTG	161436
rs752942729	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88684610	CTTAGGCTCAACAAA[C/T]ATACCTTATATAAAT	161436
rs752962146	snp	C/T	3.31741e-05	0.00407259	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625060	GCTCTCGCCACGATT[C/T]TACACAATATGTGAT	161436
rs752975229	snp	G/T			utr-variant-3-prime, downstream-variant-500B	EML5, ZC3H14	GRCh38.p7	14:88614840	TAAACCTATGGAGTG[G/T]CACACATCTAAACAA	161436
rs752977045	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88652194	CTTTGCCTCTTTATA[A/C]ATAATGAAAAACTGG	161436
rs752982819	snp	A/T	1.70101e-05	0.00291629	intron-variant	EML5	GRCh38.p7	14:88646923	CAAAGTTAGGCTTTG[A/T]AAACACAGCAAAGAG	161436
rs753000126	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88756074	GACAAGGGGAAGAGA[G/T]GGGTCTAAGATGACT	161436
rs753011904	snp	C/G	1.65677e-05	0.00287812	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621299	CCCAACAAGGATCTT[C/G]CCCTGAAACACAAGC	161436
rs753030848	snp	A/G	4.01598e-05	0.00448088	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705491	AATTACCTGTCGACG[A/G]TAGGTGAGCTGTGTC	161436
rs753060163	snp	A/C	3.36118e-05	0.00409936	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702479	GTCTTTCAAAGGATG[A/C]ATAGTTAGGCAGAGA	161436
rs753064114	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88722381	AATGCCCATCAATGA[C/T]AGACTGGATAAAGAA	161436
rs753069399	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767258	TGTACACACACCAAA[A/G]GGGCAAATCTGAAAC	161436
rs753084872	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88619356	GGCAACAAGAGCAAA[A/T]CTCCAACTCAAAACA	161436
rs753093395	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88674356	CTCACAGTTCTGTAT[G/T]TCTGAGGAGGCCTCA	161436
rs753095017	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760795	TCCATAAACATAGTA[C/T]GCCCGCCCTCCATTT	161436
rs753102522	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794400	TAAACTCTGAAAGAG[C/T]TTCCATTCTGGGCAG	161436
rs753117524	snp	A/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794232	GATATATTGGAATAG[A/T]TGTTATCCAATGTCT	161436
rs753120623	in-del	-/AAAA	3.40794e-05	0.00412778	intron-variant	EML5	GRCh38.p7	14:88646901	AATATGGAAGATGAC[-/AAAA]ATACAAAGTTAGGCT	161436
rs753121931	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701007	CACTTAGAATGCTTT[C/T]CCCCAACTTCCCCTC	161436
rs753124701	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88710551	TATGTAATTATGTGA[A/C]TTCAATTAATACATA	161436
rs753137947	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88658748	AAAATACTTACCATG[G/T]TATTTACTTATAGTA	161436
rs753169915	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88747905	CCACCCCTGCCATAA[A/T]CAGCTAGAAACTGTA	161436
rs753192719	snp	A/G	5.03022e-05	0.00501484	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661785	AAATTCCTTCACAGC[A/G]TAAACCAAGTACACT	161436
rs753195808	snp	A/C	5.2139e-05	0.00510556	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638905	GATAAAAACTCTGAG[A/C]ACCTACAAAAAAGAA	161436
rs753203556	snp	A/G			missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627813	ATGTGAATAGAAGGA[A/G]CTGTAGCTAAATAAA	161436
rs753206697	snp	A/C	1.66286e-05	0.0028834	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714959	ATTCTATAAAAAAGT[A/C]TTTTCCCATTTCCAT	161436
rs753208990	in-del	-/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791919	TTATTAGGTAAAGGG[-/T]TTCCCCCCACCCCGG	161436
rs753210792	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88643089	ACCACTGTTTTGTTG[C/T]ATACGTAATACTAGT	161436
rs753221050	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88742344	ACTGAGGAAATGAAT[C/T]TTAAGTTTCATTTAA	161436
rs753243122	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88695096	TCATACAGTAGAACA[C/T]ATTCTAACTGTACGT	161436
rs753249417	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711264	TTGTAATCCTCATGT[A/G]TTGAAGGAGAGACCT	161436
rs753249940	snp	A/G	1.70191e-05	0.00291706	intron-variant	EML5	GRCh38.p7	14:88646986	TAAAGAGGGAAAAAG[A/G]TTACAACATAAATTT	161436
rs753257176	snp	C/T	3.32557e-05	0.00407759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746189	AGAATACTTACTCTA[C/T]CTGTATGACCAGGAG	161436
rs753263876	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637169	TCCTTTCTTATTCTT[C/T]AGTCTTCCCTTGAGT	161436
rs753281294	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88724042	CTGGGAGGCCGAGGC[A/G]GGCAGATCACAGGGT	161436
rs753307139	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675965	CAACAAGTTCCTCAT[C/T]TCCATCTGAGACCAC	161436
rs753318170	in-del	-/AC	1.78223e-05	0.0029851	intron-variant	EML5	GRCh38.p7	14:88682081	TGTGTGTATATTTAT[-/AC]ACAGTTTTATTTAGA	161436
rs753329699	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88763765	ATACTCAATAAAATA[C/G]CAGGATGTTTAATTA	161436
rs753336310	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88782448	CATAAGAACGAGGAG[C/T]CAAAGGCTAATCACA	161436
rs753350297	snp	A/G	1.71343e-05	0.00292692	intron-variant	EML5	GRCh38.p7	14:88682040	TGTGTCCCTATAAAG[A/G]AAACATAGGATCAAT	161436
rs753360386	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88662689	CTGGGACTATAGGCA[C/T]ATGCCACCATGCCCA	161436
rs753373479	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88621555	TGGCAGTACACCTGG[A/C]TTCTTCAATAATCAA	161436
rs753378681	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88645074	CTTTGTCACCCAGGC[A/T]GGAGTGCCGTGGCAC	161436
rs753381690	snp	A/G			synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615821	TCTCAGCATCTCTCA[A/G]TGAGGTGTATGTACA	161436
rs753408666	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725975	AGAGAAGAAAGACTT[C/T]GTAAGTACTTATCCT	161436
rs753430125	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88776977	AAGGAGTTACTGGCC[A/T]TAAAGAGGAGCTAGA	161436
rs753433236	snp	A/G	7.54859e-05	0.00614307	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792387	GCCGACCCCCGCCAC[A/G]AAGTATACGATCTCC	161436
rs753435625	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88673735	CCTATATACCAACAA[A/C]AGAAAACAGAGAGCC	161436
rs753438681	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612938	ATTAATGCAAAAGGG[A/G]TAATAAAGACTGCAA	161436
rs753449355	snp	C/T	1.65965e-05	0.00288062	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615897	AGTTAATTATGTTTT[C/T]AGATTTTCATAACAG	161436
rs753456082	snp	C/T	0.000229289	0.0107048	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638887	TATCATCATTATGTT[C/T]CTGATAAAAACTCTG	161436
rs753460955	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677063	GCACACACCACCACA[C/T]CTGGTTAATTTTTGT	161436
rs753527965	snp	C/T	8.25389e-05	0.0064236	intron-variant	EML5	GRCh38.p7	14:88694265	TTTCAAAAGCAATAA[C/T]TTCTTAAAATTCTAT	161436
rs753540032	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88716787	GGTAACAGAGAGAGA[C/T]TGTGGTTGACTGATT	161436
rs753542387	snp	A/G	1.67038e-05	0.00288992	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621130	TATCAGCAATATCCC[A/G]AAGTCTCACTGTCCC	161436
rs753547574	in-del	-/G	1.66529e-05	0.00288551	intron-variant	EML5	GRCh38.p7	14:88616921	CATCATGGCAAGTGC[-/G]GGCAGGTTGACTATA	161436
rs753548167	snp	A/C	1.65971e-05	0.00288067	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746243	TTCCAGTCCCAAACA[A/C]AAACTGCATTCTTTG	161436
rs753571034	in-del	-/AAAC			intron-variant	EML5	GRCh38.p7	14:88631783	CTCAAAAAAAGAAAA[-/AAAC]AAAACAGAAAAACCC	161436
rs753580883	snp	A/G	2.00174e-05	0.00316359	intron-variant	EML5	GRCh38.p7	14:88618637	ACCTGGGTATACAGT[A/G]TTGGTACTGTACCTG	161436
rs753581487	snp	A/G	1.74275e-05	0.00295186	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706365	AACCCACTGATAATC[A/G]TGTGACCATCTGACA	161436
rs753667818	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88668863	ACCCAGAGCAAAAAA[A/G]CCACATTTGGAAGGG	161436
rs753672831	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768472	CTGGAGTGCAATGGC[A/G]CAATCTTGGCTCGCT	161436
rs753673517	snp	A/G	1.65616e-05	0.00287759	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688413	CCATACACTGCACAC[A/G]TCATTGTGTCATTTT	161436
rs753689102	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88703712	AAATCTGTTTCTGCC[A/G]AGCTGAAATGTGAGA	161436
rs753698376	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631683	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCGGGA	161436
rs753703894	snp	C/T			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614505	ATATATCCTGTCAGA[C/T]CAAATGGGATTCCAG	161436
rs753708220	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755913	CTGAGGTGAGAAGAT[C/T]GCTTGAACCCAGGAG	161436
rs753721174	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651729	TATTATATTTTCATA[C/T]TTATCTGTATTTATC	161436
rs753726900	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786760	CTCGTGCTGCCGCCA[C/T]GTAAGAACTGCCTTT	161436
rs753743252	snp	C/T	5.3569e-05	0.0051751	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626817	GTCAAAGTCACACTA[C/T]GTGCATTTTAAGAGA	161436
rs753743791	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756564	GGCAGATGATATGAT[C/T]ATATATACAGAAAAT	161436
rs753772482	in-del	-/AA	1.66443e-05	0.00288477	splice-donor-variant	EML5	GRCh38.p7	14:88746182	CAAAAGAGAATACTT[-/AA]ACTCTATCTGTATGA	161436
rs753814190	snp	A/G	4.28844e-05	0.00463037	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88705487	GGAAAATTACCTGTC[A/G]ACGGTAGGTGAGCTG	161436
rs753819929	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692965	GAACAGTTTCAATTT[A/G]TTGAGATTTTGATGT	161436
rs753829051	snp	C/G	3.31846e-05	0.00407323	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625089	ATCTTTCCACACACA[C/G]ACATCACCACTGATG	161436
rs753829321	snp	C/T	3.05236e-05	0.00390652	intron-variant	EML5	GRCh38.p7	14:88739038	GGAAATAAAATAATT[C/T]AACGACAAATATTTT	161436
rs753841795	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653355	AAAGTAGTGAGAGAC[A/G]GCATCCTTGTCTTGT	161436
rs753850120	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88757877	TTTATTTCAGACAGG[A/G]TCTCACTCTGTCACC	161436
rs753867369	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690228	AGGCCATTGTAAGGA[C/T]GGCCTACTTTTGCTT	161436
rs753874094	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88776118	ACCCAAGTTCTTTCA[A/G]ATATCTTGGAAAGGC	161436
rs753876800	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88636307	GAAAGCAATCCCCTT[A/G]CTCTCATGTACACCT	161436
rs753891224	in-del	-/AACT			intron-variant	EML5	GRCh38.p7	14:88693667	TACTTTTAAAAAATA[-/AACT]AATTTTAGATAATTT	161436
rs753920839	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88710280	GTGGTTCATATGATC[A/T]TTCTCTCTTTGAGCT	161436
rs753920965	snp	A/G	1.73857e-05	0.00294831	intron-variant	EML5	GRCh38.p7	14:88624926	TGCAAACCTCAGGTA[A/G]GTCACAAATGCATAA	161436
rs753925431	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88773465	ACATTGTCATATAAC[A/G]CATAATAGTAAATGA	161436
rs753926053	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88660059	GGCAGGAGGATCACC[G/T]GGGTTCAGGAGTTTG	161436
rs753965182	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88694652	CATCTATAATACCTA[C/T]TATAGTACTGTGCCA	161436
rs753989694	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88733097	TCAAGCTGCTTTATA[C/G]ACTTCTGTGCTATCA	161436
rs754003066	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88696600	TTACGTAGATAAACA[A/T]TTTTATGTTAACAGA	161436
rs754020724	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88730305	CAGAAAAATTAGAAA[A/G]TTTAAAACAGAATAT	161436
rs754022059	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88779976	TTTTTTTGAAATGGA[A/G]TCTTGCTCTGTTGCC	161436
rs754058249	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88682027	ACCTCTCCTTCCATG[C/T]GTCCCTATAAAGAAA	161436
rs754060753	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88626047	TGTGCTATTTCCTTC[G/T]GTCTCACTACCTCCT	161436
rs754062688	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88642596	TAGAATTAAAGTTAC[A/G]AACGGTTTCAACATA	161436
rs754071652	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88634683	TATGATCTTTCAATC[C/T]TCCTTTGGATAAAAA	161436
rs754079067	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88708463	TGGTGCCTGGTATAT[A/G]GCAAACACTCATTAG	161436
rs754081231	snp	A/G	1.66087e-05	0.00288168	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622677	GCACGGCACCGCCTC[A/G]GTTCCTGATCCCACA	161436
rs754107680	snp	A/G	1.65916e-05	0.00288019	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644460	CTTTTTCTTGCCTAC[A/G]TTGTTTGTCTGGAGT	161436
rs754113405	in-del	-/A	0.000238425	0.0109158	intron-variant	EML5	GRCh38.p7	14:88684984	CAATTGTATGTAAAG[-/A]AAAAAAAAACAAATT	161436
rs754115992	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780794	TGGCCAGAATGGTCT[C/T]GATCTCTTGACCTCG	161436
rs754132229	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705460	ACTTTTTAGAGAAAA[A/G]CCATGTGATATGGAA	161436
rs754139411	in-del	-/C	1.70015e-05	0.00291555	splice-donor-variant, intron-variant	EML5	GRCh38.p7	14:88646946	GCAAAGAGAGGATTA[-/C]CTGGAACCTCTTTTC	161436
rs754144617	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767385	CCCTTCTTGAGCTCC[A/G]TACCCCCTACAATTT	161436
rs754145545	snp	C/T	1.66418e-05	0.00288455	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726619	TTGACAGCTGCACAA[C/T]GAATTGGTTCTTCCA	161436
rs754147931	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88784943	TTCGGAAGCAACCTA[A/C]GAGTCTATCAACAGA	161436
rs754162872	snp	C/T	8.485e-05	0.0065129	intron-variant	EML5	GRCh38.p7	14:88643059	CATTATATTCTTCCT[C/T]ATGTATAAATGTTCA	161436
rs754188326	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88753533	GATTTTAAAGTCTAA[-/T]TATAACATAAAACTT	161436
rs754193389	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88737486	AGGGTACCTCCTGGC[A/G]AGCCTGGAGCCCAGT	161436
rs754203533	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772872	AATGGCCAAGCTCAT[C/T]ATGCTATCAAAGTCT	161436
rs754206946	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88633019	TCCCTTTTCTGTTCA[A/G]TGTAATAAACTAAAG	161436
rs754217421	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88739171	AAATCTAGAAGTAAG[C/T]CCATAAGAACTTAAT	161436
rs754225291	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88771835	TTATCAGCCCTTCCT[A/T]CTCTGTCTCCATTGG	161436
rs754234218	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88673024	AAAAGGGACTCCTCC[C/G]TAACTCATTTTTTGA	161436
rs754234515	snp	C/G	1.92684e-05	0.00310384	intron-variant	EML5	GRCh38.p7	14:88696831	TAATTCTTACTGAGA[C/G]AGCAAACAGCCTTAC	161436
rs754258199	snp	C/G	1.67708e-05	0.00289571	intron-variant	EML5	GRCh38.p7	14:88744012	ATTATAAAACAAGAC[C/G]CTTCTAGTACCTTGA	161436
rs754258765	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88634183	TCTGCTCGTTTAAAC[A/G]TGTAGTACCTCCCCT	161436
rs754263619	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88714453	ACAGGATGAATAAAT[G/T]CAGAAGATCTAATAT	161436
rs754270766	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88708581	GTAATGTAGGAAAGA[A/G]TAGTAAAGGAAACTG	161436
rs754273109	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88788371	CCACAAATAAAGAAA[A/G]TAGCTTCTACACCCT	161436
rs754276677	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88759323	TTTATCTTCATCTTG[-/T]TTTCTCACCTTCAAA	161436
rs754302601	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617817	AAAAATGGATAGTCA[C/T]GGTTACCTGTCATAC	161436
rs754307634	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88616920	TCATCATGGCAAGTG[C/T]GGGCAGGTTGACTAT	161436
rs754309411	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88652557	AATGGCCACAAATTC[A/G]CTTGAATTTTCTACA	161436
rs754313990	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88720999	AGGCAAGCAGAGAGC[G/T]AAATTATGAATGAAC	161436
rs754323938	in-del	-/CACAAATTAC			intron-variant	EML5	GRCh38.p7	14:88765121	TTTCTATGCTGATGT[-/CACAAATTAC]CACAAATTACCATAA	161436
rs754332907	snp	C/T	1.69968e-05	0.00291515	intron-variant	EML5	GRCh38.p7	14:88658428	ATCTTTCTGAGAAAT[C/T]TCATTATTTAAATAT	161436
rs754355481	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619192	CCAACATAGAGAAAC[C/T]CTGTCTCTACTAAAA	161436
rs754364830	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88657985	AGATATTTTTCATTT[A/G]TAGATAAATAATATC	161436
rs754367440	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721963	GCAAAGGACATGAGC[A/G]GACACTTTTTGAAAG	161436
rs754384094	snp	C/T	1.65704e-05	0.00287836	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658289	TTAAAGACATATCTG[C/T]ACCGCCTAGGGTAAC	161436
rs754386239	snp	A/G	1.66832e-05	0.00288814	intron-variant	EML5	GRCh38.p7	14:88688221	TTCTTAAAATGCTCT[A/G]CACTCCAGGACAAAT	161436
rs754392223	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750427	ATAACCATAGTTAAA[C/T]GGGGACAAATAAAAA	161436
rs754442319	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88758015	GTGCCACCACACCTG[A/T]CTAATTTTTTTTTTT	161436
rs754477602	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88676357	GCACCTTCTTCACAG[G/T]GTGGCAGGATAGAGT	161436
rs754478278	snp	A/C	1.65985e-05	0.00288079	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625097	ACACACAGACATCAC[A/C]ACTGATGGTACCTGT	161436
rs754480154	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785183	GATGGTTACCAGAAG[C/T]TGGAAAGGGTCGTGG	161436
rs754482574	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711516	CCATTTATAAAACCA[C/T]TGGATCTCGTGAGAA	161436
rs754520150	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764901	AATTCTTTTAAATTT[A/G]TTAAGGTTTGTTTTA	161436
rs754530051	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88782808	GCCTGGATCGGGCAC[A/G]GTGGCTCACATCTGT	161436
rs754535400	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88622958	CTTTTTTTCTGACAT[A/G]AGCATAATTTTATTT	161436
rs754539725	snp	C/T	1.70272e-05	0.00291776	intron-variant	EML5	GRCh38.p7	14:88646990	GAGGGAAAAAGATTA[C/T]AACATAAATTTGAAT	161436
rs754539822	snp	A/G	1.66585e-05	0.00288599	intron-variant, utr-variant-3-prime, synonymous-codon	EML5	GRCh38.p7	14:88616101	TAAGTCTCTTAACTA[A/G]TAACATAGTCTGCTC	161436
rs754575549	in-del	-/AAAG			intron-variant	EML5	GRCh38.p7	14:88640169	AGGTAGAAAACTAAC[-/AAAG]AAATTCTGGACTTGA	161436
rs754576737	snp	C/T	1.65669e-05	0.00287805	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736538	AGAATGTGGTCACCT[C/T]GCCAACACACACTCC	161436
rs754592669	snp	C/T	3.57309e-05	0.0042266	intron-variant	EML5	GRCh38.p7	14:88681866	TGAGAGCTTAATCTA[C/T]GTTCAAGTGTGAGAG	161436
rs754624492	snp	C/T	2.35114e-05	0.00342858	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615768	GTTTTGGTTTTTCTT[C/T]TCTGTAATTCTGGTC	161436
rs754626640	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88782316	AGAAATTTCTAAGCG[A/G]CAAAGAATTCAAGAG	161436
rs754639969	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88645223	TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC	161436
rs754646324	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88699000	CCAGTAGCGAATAAG[G/T]GGAAAGGCTTGGATT	161436
rs754688358	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735069	AACAGAAATATTTAC[A/G]GATGAAATCAGGGAA	161436
rs754698822	in-del	-/GTGAGCT			intron-variant	EML5	GRCh38.p7	14:88719327	GAGTTCGAGGCTGCA[-/GTGAGCT]GTGAGCTGTGATTGT	161436
rs754721946	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88669061	AGTGACAGCCCACCT[A/G]GGAGCTGCACAGGAC	161436
rs754723942	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88650433	CACTCCAGCCTGGGC[A/G]ACACAGCAAGACTCT	161436
rs754735500	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88751149	AAACCAACATCCCTA[C/T]GCATAGATTACGCAA	161436
rs754780998	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88739986	AAAACGCTAAGAATT[G/T]AAACAGCAGATTTCT	161436
rs754795781	snp	C/T	1.99874e-05	0.00316122	intron-variant	EML5	GRCh38.p7	14:88618638	CCTGGGTATACAGTA[C/T]TGGTACTGTACCTGG	161436
rs754803350	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88635085	AGAAAATGTGAAAGC[A/T]CATGCTCATTATATT	161436
rs754819314	snp	C/T	0.000121058	0.0077791	intron-variant	EML5	GRCh38.p7	14:88663168	TAAAATACATACAAA[C/T]ATATATACCATCAGT	161436
rs754832886	snp	C/G	1.65616e-05	0.00287759	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688415	ATACACTGCACACAT[C/G]ATTGTGTCATTTTTC	161436
rs754852115	snp	G/T	1.75511e-05	0.0029623	intron-variant	EML5	GRCh38.p7	14:88694266	TTCAAAAGCAATAAT[G/T]TCTTAAAATTCTATG	161436
rs754868894	snp	C/T	3.31983e-05	0.00407407	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746248	GTCCCAAACACAAAC[C/T]GCATTCTTTGAATCA	161436
rs754874082	snp	C/T	1.8337e-05	0.0030279	intron-variant	EML5	GRCh38.p7	14:88661845	CCTAAAAATGAAAAA[C/T]AATGCTGTAAGTTTG	161436
rs754893456	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88665569	GGTGGCTCATGCCTA[-/T]TAATCCAAGCACTCT	161436
rs754905502	snp	G/T	1.75452e-05	0.00296181	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706366	ACCCACTGATAATCA[G/T]GTGACCATCTGACAT	161436
rs754946144	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88694876	TTAAAATCTCTGACA[A/C]TGTTGACTAGTTCCT	161436
rs754956166	snp	C/T	1.66435e-05	0.0028847	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626852	CTGCACCAAATGCAA[C/T]AGCGAGCATGGTCTG	161436
rs754957932	snp	A/G	1.78717e-05	0.00298923	intron-variant	EML5	GRCh38.p7	14:88618370	ACAAGAATTCCATTA[A/G]GTGAGAGACAAAATC	161436
rs754993714	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674649	ACTTCCCAAATTTCA[C/T]GTCCTCACATTTCAA	161436
rs755010958	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88775318	GTGGGATCTTTGGGT[A/C]CCCAATTCCAGAACC	161436
rs755016990	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88679319	AATGAATTATAATTT[C/T]CTTCTACAAATCATA	161436
rs755019360	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88750474	CTGTGAAAATTGACA[G/T]ATGTACTACTTAAAG	161436
rs755030047	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88648707	CTCCCTTCCTCCTGT[A/G]CTTTCTTCTAGCCCA	161436
rs755043260	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652611	TTCCCTTTTAATTTC[C/T]CCCTCAAATTGTCCA	161436
rs755046095	snp	C/T	8.28535e-05	0.00643583	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658292	AAGACATATCTGTAC[C/T]GCCTAGGGTAACCAA	161436
rs755051180	snp	A/G	1.66549e-05	0.00288568	intron-variant	EML5	GRCh38.p7	14:88616921	CATCATGGCAAGTGC[A/G]GGCAGGTTGACTATA	161436
rs755065063	snp	C/T	4.21683e-05	0.00459155	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687254	GCTCTTTTTATAGCA[C/T]AGGTCTTGAGACATC	161436
rs755065537	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88641032	GGAGATGGATAAATT[A/C]CTAGAAACACACAAC	161436
rs755068983	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88680991	ATGAGATCCTTGGAG[A/G]CAATTAGATTTTATA	161436
rs755070774	snp	C/T	1.65671e-05	0.00287807	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740478	TATGTTAATTCATCC[C/T]TTGCACAGGCTAGGC	161436
rs755083074	in-del	-/TCCTGC	2.47185e-05	0.00351549	cds-indel, nc-transcript-variant	EML5	GRCh38.p7	14:88739009	ATTCATGCTAAAAAT[-/TCCTGC]CTAGAAGAGGAAATA	161436
rs755106593	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88776158	GACAGGTACAAACAA[A/G]CTCAGATAGTGAAGA	161436
rs755118069	snp	A/T	4.98882e-05	0.00499416	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704937	ACTTTTTTGTTTCTC[A/T]TTGCACTGTTCTTTA	161436
rs755120507	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642690	TATGAATTCCTTTTC[C/T]GCTGTATTATACTCT	161436
rs755132834	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88780034	GGCTCACTCTGTAAC[A/C]TCCACCTCCCAGGTT	161436
rs755141186	snp	A/G	1.72997e-05	0.00294101	intron-variant	EML5	GRCh38.p7	14:88624934	TCAGGTAGGTCACAA[A/G]TGCATAAATATTCTG	161436
rs755142877	snp	C/G	1.6574e-05	0.00287867	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616822	TACACAGGCACAGTT[C/G]ACATCAGCTTTCTCA	161436
rs755150737	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612186	TCCCAAAGATTATAT[A/G]ATGTTCATAATCCAC	161436
rs755242897	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88671998	TTAGATCATAAAGAC[A/G]GAAAATTAACAAAGA	161436
rs755245411	snp	A/T	4.97236e-05	0.00498591	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626884	ATCCGGGCATCTTCC[A/T]GTGTGCTCAGTAGCC	161436
rs755251052	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668785	ATCCTTTAAAATTCA[C/T]AGCTGAGATCATTGA	161436
rs755261678	snp	A/G	4.68154e-05	0.00483792	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726620	TGACAGCTGCACAAC[A/G]AATTGGTTCTTCCAT	161436
rs755278815	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687461	AAGAACAGGAATTAG[C/T]TTAAGAATCCATTGT	161436
rs755299800	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88696359	AACTTTTAAACAAAC[-/AG]AAAAGCGCTAATATG	161436
rs755300657	snp	C/G/T	4.98569e-05	0.00499263	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622687	GCCTCAGTTCCTGAT[C/G/T]CCACAGTTTAACCGC	161436
rs755317030	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768493	TTGGCTCGCTGCAAC[G/T]TCCACTTCCAGGGTT	161436
rs755318280	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88753570	ATTATAAATGAACAA[-/C]CTGCAAGATCCAACT	161436
rs755369400	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88655642	GGATCTAATTAAACT[A/G]AAGAGCTTCTGCACA	161436
rs755384492	snp	A/G	2.04468e-05	0.00319734	intron-variant	EML5	GRCh38.p7	14:88696969	TAAAATAGAATTATA[A/G]AAGCTATTAAATACA	161436
rs755390370	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88721270	GAAAAAAACTACTTA[A/C]GACATCATATGGAAC	161436
rs755421893	snp	C/T	1.70968e-05	0.00292371	intron-variant	EML5	GRCh38.p7	14:88658432	TTCTGAGAAATTTCA[C/T]TATTTAAATATTTCC	161436
rs755433517	snp	G/T	3.6551e-05	0.00427483	intron-variant	EML5	GRCh38.p7	14:88696840	CTGAGACAGCAAACA[G/T]CCTTACCTGAGAAAT	161436
rs755434981	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623565	AGCTGGGATTACAGG[C/T]ACCATGCCTGGCTAA	161436
rs755437246	snp	A/G	1.66507e-05	0.00288532	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714952	ACCTGGCATTCTATA[A/G]AAAAGTCTTTTCCCA	161436
rs755439632	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88791315	ATTTTGTAACCAAAC[C/T]CAAATCGTAGAATCT	161436
rs755448068	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88760653	ATTCTAATTACTTCA[A/T]CTTTCCTATAAAGTT	161436
rs755449428	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88711376	GTTTAAAAGTGTTCA[-/G]CAGTTCAGCATGGCT	161436
rs755456351	snp	A/G	2.26185e-05	0.00336285	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627771	CATCTTAGGATAGAT[A/G]AAGTCTGCTTGTTCA	161436
rs755498641	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788377	ATAAAGAAAATAGCT[C/T]CTACACCCTTCATTT	161436
rs755499438	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88791595	AAAAATAGCCCCCCA[A/G]TAGCGATTTAATTTT	161436
rs755510877	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88673660	AAAGCTTCTTAAGCT[A/G]ATATGCAACTTCAGC	161436
rs755515962	in-del	-/T	7.20812e-05	0.00600295	intron-variant	EML5	GRCh38.p7	14:88621400	CTGCTTTCAGAGAAC[-/T]TTTTGCTTTGAGCTA	161436
rs755530994	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692967	ACAGTTTCAATTTAT[C/T]GAGATTTTGATGTCA	161436
rs755537868	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747049	CCTAAATGAAGTACC[A/G]CAACTTTGATCTATC	161436
rs755577845	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88760198	ATCTAGTTCATTGAC[-/TT]TTGTTTTATGGACCA	161436
rs755583670	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778892	TAACAGGATTTCATT[C/T]TTGGGCTTCTTTGTG	161436
rs755615701	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741035	AGGTATGGTGGCGCA[C/T]GCCTGTAATCCCAGT	161436
rs755620076	snp	A/T	1.65999e-05	0.00288091	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644501	GTGGTGGGGCCCTGC[A/T]CACTGGAGGCCTGCA	161436
rs755669483	snp	C/T	1.65902e-05	0.00288008	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665435	AAGAAGCTTCCATCG[C/T]TGAGACCTACGGCTA	161436
rs755689168	snp	C/T	0.000148765	0.00862325	missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792380	ACACCACGCCGACCC[C/T]CGCCACGAAGTATAC	161436
rs755696030	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710801	TATGTCCTTGAAGGA[A/G]TGAATAATCTCTTAG	161436
rs755746314	snp	A/G	1.75789e-05	0.00296465	intron-variant	EML5	GRCh38.p7	14:88754703	TAAATAAGTAGTATT[A/G]TTAAAAATTGCTTAT	161436
rs755749478	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711386	GTTCAGCAGTTCAGC[A/G]TGGCTGGGGAGGCCT	161436
rs755758206	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762338	CAACACAGAGAAACC[C/T]AGTCTCTAATAAAAA	161436
rs755817551	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88642155	ATTCAGGATGAAGCT[A/G]TCAGAGGAAAACCAG	161436
rs755825999	snp	C/G	3.53251e-05	0.00420253	intron-variant	EML5	GRCh38.p7	14:88621387	TGACCCTATTGACCT[C/G]CTTTCAGAGAACTTT	161436
rs755843591	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767243	TGCAGTGCTACCACA[C/T]GTACACACACCAAAG	161436
rs755875584	snp	C/G/T	0.000119369	0.0077248	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620863	CAATAGCCACCATGT[C/G/T]CCCTTCAGGGCTGTA	161436
rs755885360	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748021	TAAGTCCTGTAATCA[C/T]CCGAGCTTCCATCTA	161436
rs755899371	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88629333	AAATTCAATGACTGA[A/G]CTTCTCATATTTTTA	161436
rs755904352	snp	G/T	1.65866e-05	0.00287976	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625072	ATTCTACACAATATG[G/T]GATCTTTCCACACAC	161436
rs755921077	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88618344	GACCTTTTTCATCAG[A/T]TTAAAATGGGACAAG	161436
rs755925753	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88667865	TCTCTGGCAGGAGTC[C/T]TCACAGTTCAATGAT	161436
rs755940611	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88727719	ATGCATTTTTAAACA[A/G]TGCAGTACATTGATT	161436
rs755962863	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88754731	TATACAGATTTTATA[A/G]TATTTGGTAGATGTA	161436
rs755965213	snp	C/T	1.71655e-05	0.00292958	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661695	CAAATCCCAAATCGT[C/T]CCCGGTAGCTAGAAC	161436
rs755973252	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715257	GAATTAATGCCGTTT[C/T]AAACATGTCTAAAAT	161436
rs755991975	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757315	ATACCTCAAACCATA[C/T]ACAAATGTCAACTCA	161436
rs755992232	snp	A/T	1.70095e-05	0.00291625	intron-variant	EML5	GRCh38.p7	14:88646970	TCTTTTCAGCAGCAG[A/T]TAAAGAGGGAAAAAG	161436
rs755992465	snp	C/T	1.66665e-05	0.00288669	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624978	GACTCACGGCCTTTC[C/T]TTTCCCCCAGTCACG	161436
rs755995256	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88785441	AAACATCTCATGTAC[C/G]CCATAAATAGATAAA	161436
rs756002017	in-del	-/CAAA			intron-variant	EML5	GRCh38.p7	14:88737134	GAACTTGGAACTCAC[-/CAAA]CAGTGAGTACAGACA	161436
rs756010049	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88702216	ATAAAACAAGCCAGA[A/G]CTATGAGTTCCAAAT	161436
rs756021776	snp	C/T	1.6563e-05	0.00287771	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736527	GTGTTCCAACTAGAA[C/T]GTGGTCACCTCGCCA	161436
rs756022327	snp	A/G	1.65726e-05	0.00287855	intron-variant	EML5	GRCh38.p7	14:88688262	TTAAAATCTCTTTAG[A/G]TTACTTACTTTTTCC	161436
rs756095818	in-del	-/TTAT	3.52715e-05	0.00419935	intron-variant	EML5	GRCh38.p7	14:88696991	TTAAATACAATTAAA[-/TTAT]TTATTTCCATATCTA	161436
rs756114543	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88744984	CATATCAATGCAACT[C/T]TGAAATATTCAACCA	161436
rs756120251	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786649	AGATAATTTGAATCA[C/T]GGGGGCAGTTTCCCC	161436
rs756134753	snp	A/T	0.000298706	0.0122173	stop-gained, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616233	GACCCAAGAACCTTT[A/T]GTGTTTTGCCTAAAA	161436
rs756139874	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703571	ACTGCATAGAAACTA[C/T]TGCCATTTTAACACT	161436
rs756140251	in-del	-/ATTTTA			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612687	AGATTTAAATAGTAT[-/ATTTTA]ATTTTAAATGACAGA	161436
rs756149390	snp	A/C	0.00016749	0.0091497	intron-variant	EML5	GRCh38.p7	14:88621885	TGATGGAAACTTTCA[A/C]AATCCTCTCTTGTAA	161436
rs756176193	snp	A/G	1.65855e-05	0.00287967	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685106	CCATGTCCTAATGAT[A/G]TGGCACGTATAGATG	161436
rs756187588	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88732873	TGGAGTGCAGTGGCG[C/T]GATCTCAGCTTATTG	161436
rs756189608	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88744501	CTTTATAGCTTTCTA[A/T]CACTCAGAACTGTTT	161436
rs756203892	snp	A/G	1.66051e-05	0.00288137	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622666	CAAGCCTGAAGGCAC[A/G]GCACCGCCTCAGTTC	161436
rs756233305	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692781	CTTTGTAAACGCATA[C/T]GCTGTTATCTGATGA	161436
rs756239019	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88728452	AAACAGTTGTTTAAC[A/G]TACACTTTGTGCATT	161436
rs756241457	snp	A/G	3.30562e-05	0.00406534	intron-variant	EML5	GRCh38.p7	14:88726504	TTCTGTATCACTGAA[A/G]ATAAAATTATTATGT	161436
rs756272058	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88729090	ATATAAACACATCAT[-/AT]ATATATATATAACCA	161436
rs756294239	snp	A/G	1.69758e-05	0.00291335	intron-variant	EML5	GRCh38.p7	14:88754508	ATGAAAAACTGTCAC[A/G]TACCTGTCCATCTAA	161436
rs756309975	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88746835	ACAAATAACCCCTTC[A/C]TAAAGAAGCGGAGGC	161436
rs756348768	snp	C/T	1.65872e-05	0.00287981	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642968	CATTTAAATAGTGAA[C/T]ATTATTCCTACAGTC	161436
rs756371698	snp	C/T	5.3527e-05	0.00517307	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715100	TCAACCGAGCTGTCA[C/T]TGCATCCAACAGCAA	161436
rs756372704	in-del	-/CAGAAGGTTGGGCTCTCCAGGAA			intron-variant	EML5	GRCh38.p7	14:88691157	TCAGCTGCCCAAATT[-/CAGAAGGTTGGGCTCTCCAGGAA]CAGAAGGACACACTA	161436
rs756375503	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88730240	AAGGATACAAATATA[C/T]ATTACCAGACTAAGC	161436
rs756396097	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88625795	TCAATAGTCTTTTTC[C/T]CAAAAATGTAAGTGT	161436
rs756405058	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88620197	CTTTTGACAGACCTA[C/G]ATTCAATAATCTTAT	161436
rs756419136	snp	A/G	1.82891e-05	0.00302394	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695430	CTATCATCTATGCCA[A/G]CTGATGCCAAACGTT	161436
rs756422255	in-del	-/G	1.71443e-05	0.00292777	intron-variant	EML5	GRCh38.p7	14:88624949	ATGCATAAATATTCT[-/G]TGAAAAGAAAGAGGA	161436
rs756427249	snp	A/G	1.72454e-05	0.00293639	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627703	GTCCCACAGACAGCA[A/G]TAGTTTGCCAGTAGC	161436
rs756433865	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88630140	GGTTCAAGTGATTAT[A/C]CTGCCTCAGCCTCCA	161436
rs756461890	snp	A/C/T	3.31434e-05	0.00407073	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658285	ACCATTAAAGACATA[A/C/T]CTGTACCGCCTAGGG	161436
rs756472987	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779878	ATTTCCAATTCAAAT[C/T]CAGAACTACAAAATT	161436
rs756510676	snp	C/T	1.66496e-05	0.00288522	intron-variant	EML5	GRCh38.p7	14:88627061	CCTGACAAGATACAA[C/T]AAAATTATCTAGGTT	161436
rs756524365	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692859	CATGTAATTTACAAC[C/T]TGAAAGTTACTTGAA	161436
rs756524755	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783425	TCCACTGATCCAAGA[A/G]ACACACTTCACCTAT	161436
rs756534288	snp	A/G	1.67778e-05	0.00289631	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712422	TTCAAGGCCTGAAAC[A/G]CATGTCCATGAAGCC	161436
rs756544386	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88757537	TAGTAATGCAACCCA[A/G]AGAATGGGAGAAAAT	161436
rs756548128	snp	A/C	2.38626e-05	0.00345409	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687233	TTAGATCCTGGGGCC[A/C]ATGCAGCTCTTTTTA	161436
rs756548371	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88771796	TTGAAAGACTTTCCT[C/T]TCTAGGCTTCCTGAC	161436
rs756556284	in-del	-/GAAAA			intron-variant	EML5	GRCh38.p7	14:88751700	GAATGTAAGTAAAGT[-/GAAAA]GAAAAGGCTACAGAC	161436
rs756581902	snp	A/C	1.65875e-05	0.00287984	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658221	AATGTCGGATTCTTC[A/C]CTATCACAAGGCCTT	161436
rs756585798	snp	A/C/T	3.3288e-05	0.00407959	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712358	TATAATTTCCATCTA[A/C/T]TGAATTTATATCGTT	161436
rs756586828	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720910	AGCTTCTTAAGCTGA[C/T]AAGCAACTCCAGCAA	161436
rs756587756	snp	G/T	1.71997e-05	0.0029325	intron-variant	EML5	GRCh38.p7	14:88740579	ACTCCAGAACTAAAA[G/T]GTATATAGTATAATC	161436
rs756601775	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88671220	GACCTCTCAGCAGAA[A/G]CCCTACAAGTCAGGA	161436
rs756607579	snp	C/G			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616397	TCAGCATGAGTAGTG[C/G]ATCTGCAAAACCAGG	161436
rs756618128	in-del	-/TAGGCTTTGTAA	1.702e-05	0.00291714	intron-variant	EML5	GRCh38.p7	14:88646914	ACAAAAATACAAAGT[-/TAGGCTTTGTAA]ACACAGCAAAGAGAG	161436
rs756642672	snp	C/T	1.65756e-05	0.00287881	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740457	TCCCCATTGAGTGCA[C/T]CAGAATATGTTAATT	161436
rs756654595	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88648294	AAAGCCATTCATATC[C/G]AAGATAACAATGATA	161436
rs756655230	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88654271	AAGGGTTTTTTGTGT[C/T]TCTCTCTCCTTCAGT	161436
rs756662666	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88617753	TACAGGCATGAGCCA[C/G]TATATGCCTGGCTGA	161436
rs756723036	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701834	TGAAGGAAATAATTT[C/T]ACTCTCACATGGTTG	161436
rs756726697	snp	A/G	0.0003803	0.0137843	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705571	CTGATTCATCACTAT[A/G]AGAGTCAGCCAGACT	161436
rs756726821	snp	A/T	1.74476e-05	0.00295356	intron-variant	EML5	GRCh38.p7	14:88754500	AGAAAAAAATGAAAA[A/T]CTGTCACATACCTGT	161436
rs756735002	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88790202	ATTCTCAGTATCATA[A/T]TAAATTTGTGCCACC	161436
rs756773492	snp	A/G	0.000107152	0.00731879	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620850	CCATTTTTCATTCCA[A/G]TAGCCACCATGTCCC	161436
rs756777940	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88648352	CAAGATTCCCAGAAT[A/T]ATAATTATTATATTT	161436
rs756805276	snp	C/T	1.78252e-05	0.00298534	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695410	CCCAGAGCACAACAG[C/T]ATGGCTATCATCTAT	161436
rs756826110	snp	C/G	8.55395e-05	0.0065393	intron-variant	EML5	GRCh38.p7	14:88618845	GTAAAAAGTATTAGA[C/G]CACATGAAGTATTAT	161436
rs756826662	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88659241	GGAATGACGACTCTC[-/T]TTTTTTTTTTTTGAT	161436
rs756830885	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88649762	CTAAAAATGCAACTC[G/T]TTTATAGAATTTGTC	161436
rs756832897	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633407	AGGTGTGAGCCACTA[C/T]ACCCCACCTGTCATC	161436
rs756843131	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668576	TGGGTTATGGAGCTA[C/T]TGTCATGTGAACACA	161436
rs756846867	snp	A/T	1.71067e-05	0.00292456	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754577	CCTTTAAAACTGATA[A/T]GGTCTGCACAGTGTA	161436
rs756850352	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88739605	AGAATAACATTTAGG[A/T]AACTTTGGGCTGTGA	161436
rs756853090	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687709	TTATATATAAACAGC[C/T]GATTTTTGACACATA	161436
rs756855380	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88785101	AGAAAGACAAACATC[A/G]CATGTTCCCACTTAT	161436
rs756863471	snp	C/T	1.70571e-05	0.00292032	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627670	ATCTCCAAATGGTAA[C/T]AGTATGTTCTGGGTC	161436
rs756864102	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88722416	TGGTACATGTATACC[C/T]TGGAATACTATGCAG	161436
rs756868455	snp	G/T	2.14977e-05	0.00327848	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706399	GTTACGTGAGCTGAA[G/T]GGCCAATATATTTTC	161436
rs756881175	in-del	-/A	1.86555e-05	0.00305408	intron-variant	EML5	GRCh38.p7	14:88618189	TTCTAACTGGCCTTC[-/A]AAAGTCAGTTCTTGC	161436
rs756883572	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721501	CAACAAACCTGACAA[A/G]AACAAGCAAGGGGGA	161436
rs756891505	snp	A/G	1.6674e-05	0.00288734	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712317	TATAATTCCATAGTC[A/G]TCAGCTGTAACTAAA	161436
rs756900947	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88619418	GGCGGGGTCTCACTA[G/T]GGTCCCAAACTCCTG	161436
rs756922441	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88618061	AAACATGGAAATATA[C/T]TCAATAAAAAGGGGT	161436
rs756929625	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760862	TTTTAGTATATAACA[C/T]AGACCTTGCATAGAT	161436
rs756949196	snp	C/T	3.33406e-05	0.00408279	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740422	TTCGTATAAGATTGA[C/T]TCCTTTCCAAACATA	161436
rs756959524	snp	A/T	0.00159681	0.0282109	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88634477	TCCTTACCTGACATG[A/T]CTGCTGAATCACCTA	161436
rs756999815	in-del	-/AAAC			intron-variant	EML5	GRCh38.p7	14:88771047	AGGAAATAACATGTT[-/AAAC]AAACATAAAGTGAGC	161436
rs757009157	snp	A/G	3.33256e-05	0.00408187	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88622701	TCCCACAGTTTAACC[A/G]CTCCTCCTTCTTTTG	161436
rs757020565	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88677460	GGCAAATGGGATCTA[A/G]TTAAACTGAAGAGCT	161436
rs757023015	snp	C/G	1.65836e-05	0.0028795	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88627022	ATACGTTGATTGTGA[C/G]CAGCTCTGCTGGCAA	161436
rs757027789	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778647	AGCTGGGCAATGTGG[C/T]GCACGCCTGTAGTCC	161436
rs757035445	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88696180	ATATATATATATATA[C/T]ATATATTTCCCTCTG	161436
rs757038752	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639356	TTTGGCTGAAGTGTA[A/G]GGTCATGAAGAAGAA	161436
rs757056219	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678932	AATCTGAAATCAAGA[C/T]GTTGGCAGAGCTATG	161436
rs757058565	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88624390	TACATGTCATGTTTC[A/G]ACATGCATATGACTA	161436
rs757062363	in-del	-/A	5.27422e-05	0.00513501	intron-variant	EML5	GRCh38.p7	14:88704836	AAAATTCAAACAAAT[-/A]AATGAAAGATAGTTG	161436
rs757062890	snp	A/G			intron-variant, missense	EML5	GRCh38.p7	14:88765409	GCTCACCTCCTCAAG[A/G]CCAACTGCATGCCTC	161436
rs757065715	snp	A/G	1.6968e-05	0.00291268	intron-variant	EML5	GRCh38.p7	14:88624957	ATATTCTGTGAAAAG[A/G]AAGAGGACTCACGGC	161436
rs757082854	snp	A/C	1.73366e-05	0.00294415	intron-variant	EML5	GRCh38.p7	14:88644389	TTTTATAAAAAAGAA[A/C]TCTGGATACATTTCA	161436
rs757100339	snp	C/G	3.43731e-05	0.00414552	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705511	TGAGCTGTGTCTCTT[C/G]TTCAATTTCAGAATC	161436
rs757114299	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88727931	TTGTTTGAAAATTAA[A/G]AATTATACTTCCATA	161436
rs757143565	snp	A/G	1.67391e-05	0.00289297	intron-variant	EML5	GRCh38.p7	14:88664666	ATTTTCTATCTTTGG[A/G]AATACTTTTTTACAC	161436
rs757150137	snp	C/T	4.81591e-05	0.00490686	intron-variant	EML5	GRCh38.p7	14:88754692	AAATAAGGAAATAAA[C/T]AAGTAGTATTATTAA	161436
rs757155268	snp	C/T	1.66732e-05	0.00288727	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704956	CACTGTTCTTTAAGC[C/T]GAGGTAGATCTTCTT	161436
rs757161621	snp	G/T	1.65619e-05	0.00287762	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736481	GGTTTATTTCTTTCT[G/T]GCACCACAATTTCAA	161436
rs757188559	in-del	-/A	3.92457e-05	0.00442959	intron-variant	EML5	GRCh38.p7	14:88754486	TAACATACAATTTAG[-/A]AAAAAAATGAAAAAC	161436
rs757216615	snp	A/G	1.76281e-05	0.0029688	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726657	CCTTGCTATTAATGC[A/G]TGATCTACTAGGCTC	161436
rs757229946	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88637610	AGCCCATATCCCCAG[A/C]ACCTAAAACAATACC	161436
rs757238895	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752984	CCCTTCAATCTGTTC[A/G]TGTAACCTGGTTCTT	161436
rs757258243	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88644028	AGGAGAAACAGGCTT[-/C]ATGAACCCTGTACAG	161436
rs757258580	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88757212	GGTGGTGCCAAGACA[A/G]TTCAATGGGGGATAA	161436
rs757275729	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672567	CAGAACTGAAGGAGA[C/T]AGAGACACGAAAAGC	161436
rs757288475	snp	C/G/T	1.66261e-05	0.00288319	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714961	TCTATAAAAAAGTCT[C/G/T]TTCCCATTTCCATCA	161436
rs757308775	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88783893	TGGATTATTCTCAAG[C/G]ATAGACTGTGTGTTG	161436
rs757310119	snp	A/C	6.5822e-05	0.00573643	intron-variant	EML5	GRCh38.p7	14:88638925	ACAAAAAAGAATTTG[A/C]GAATTAAGTTTGAAA	161436
rs757311934	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88701306	GTCAGCCTCCCACAA[C/G]AAATAATTACCTGCC	161436
rs757327923	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705158	AAATTCACATTTTCT[A/G]CATATCACACTGACA	161436
rs757333637	snp	A/G	1.67295e-05	0.00289214	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642928	ATTCCAACAGATGCA[A/G]TGTGATAAATTATAT	161436
rs757346010	snp	C/G	1.67525e-05	0.00289413	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702489	GGATGAATAGTTAGG[C/G]AGAGAATATCATCAT	161436
rs757347021	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88654024	TTGGGAGGGTGTATG[C/T]GTCCAGGAATTTATC	161436
rs757364736	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706721	GTTTTGGCCTGAGGC[C/T]TTTGGGCTTAAGTGA	161436
rs757376086	snp	A/G	1.6601e-05	0.00288101	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746210	TGACCAGGAGCCATA[A/G]ACAACATTTTTCCCC	161436
rs757392366	in-del	-/TAC	0.000119154	0.00771769	cds-indel, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88649913	ATAAAACACTTACCT[-/TAC]TACTACTCCCTGCCT	161436
rs757398739	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638243	TGGCTGTAGAGTTAT[A/G]GCCTTTGTTTAACAG	161436
rs757457689	snp	A/G	2.03052e-05	0.00318625	intron-variant	EML5	GRCh38.p7	14:88618632	TTGCCACCTGGGTAT[A/G]CAGTATTGGTACTGT	161436
rs757458435	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88758879	GAACCTTGAAAACAT[A/T]ACGCTAAGTGAAGGA	161436
rs757462156	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88658884	GAAATAGATACAATA[A/G]TTGAGAAAGGATACA	161436
rs757477344	snp	A/G	1.6855e-05	0.00290297	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88744083	CAAATCCCAAGAAAT[A/G]TCAAATATCTGTAAA	161436
rs757478513	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725415	AGAAAACATAATGTA[C/T]CTGTTCATAATGGGG	161436
rs757487194	in-del	-/AAAAAATAAAAAT			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679690	GAGCAAGACTGTCTC[-/AAAAAATAAAAAT]AAAAAATAAAAAAAT	161436
rs757505996	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691391	TTTGGCCTAGAAAGC[C/T]TAAAATATTTACTAT	161436
rs757511459	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88744779	CTGCTTTCTGGTAGT[C/T]GTCATGTTTCTTTGA	161436
rs757520847	in-del	-/A	0.000238425	0.0109158	intron-variant	EML5	GRCh38.p7	14:88684985	CAATTGTATGTAAAG[-/A]AAAAAAAACAAATTA	161436
rs757526112	snp	C/T	6.63867e-05	0.00576099	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658211	CTTCAGAATCAATGT[C/T]GGATTCTTCACTATC	161436
rs757530034	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733509	CAGTAGTCTGAACAA[C/T]TACTTTTTAAAGAAA	161436
rs757536675	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777364	TCAACATGAAGGAGA[A/G]ACAAAGACTTTCCCA	161436
rs757543517	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88628867	ATCATTAAGTAGAAA[C/T]TGTTCAAAGATTTAT	161436
rs757569870	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88643407	AAATAACATTTAAAA[C/T]ACAATATTGTATAAC	161436
rs757581221	snp	C/T	1.65748e-05	0.00287874	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685068	CTAGTATTTCACCAT[C/T]CTTTGTGCCAACTAA	161436
rs757591002	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790893	GCTATTATAATAGGT[C/T]TGTAACCCTAATCAC	161436
rs757625138	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644874	TGCCACCACACCAGA[C/T]AATTTTTGTATTTTT	161436
rs757632333	snp	A/G	6.48179e-05	0.00569252	intron-variant	EML5	GRCh38.p7	14:88740357	TAAGTAATACACATG[A/G]AAGTGTTTAAAATAC	161436
rs757633146	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88677797	ACAGTCAAGAAACAA[G/T]AGATGGTGCTAAGGC	161436
rs757647343	snp	C/G	1.65971e-05	0.00288067	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616225	GGGCGAATGACCCAA[C/G]AACCTTTTGTGTTTT	161436
rs757647357	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88781152	GGGTTTAGGCGGGCA[A/C]AGATGACTGATACAA	161436
rs757664303	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88749645	AACAGAAGAAAGGAA[A/G]CAGCAGAATATACTT	161436
rs757694446	snp	C/T	3.75256e-05	0.00433144	intron-variant	EML5	GRCh38.p7	14:88702653	ATAGAAAACAAATCA[C/T]ATATAATTAATTTTG	161436
rs757696309	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88742512	TAACTCATTATAAAA[-/AT]ATAGTTTATTTAGTT	161436
rs757698910	snp	C/T			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615682	AGATCAGTCTTTCAC[C/T]ATTTTGATGATTCTG	161436
rs757712195	snp	C/T	1.68883e-05	0.00290584	intron-variant	EML5	GRCh38.p7	14:88684973	TATTGAAATAATCAA[C/T]TGTATGTAAAGAAAA	161436
rs757720654	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88768792	AAGTTATCTTTTCTA[C/T]TTATTTATTTAACCC	161436
rs757727607	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88618023	CCTTAAAAAAAAAAC[-/TT]GATAAATCATGGAAA	161436
rs757734172	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88617843	CATACAGCCAGGAAA[-/T]TTGAACAAATTTGGA	161436
rs757745731	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88645383	CAGCACAAGAGTAGA[C/T]TGTTTATAAACAAAT	161436
rs757748735	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630740	AGGATTTTTAGGTCA[C/T]GGCTCTGAAAAGGAT	161436
rs757771911	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88629856	TGTAGCTCCCTCCAG[A/G]AAATCAATCCCAGTA	161436
rs757783990	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88717685	ACTTGAACTCGGGAG[G/T]CAGAGGTTGCAGTGA	161436
rs757800705	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674402	TAGCAGAAGGCAAAG[A/G]AGAAGCAGGCACCTT	161436
rs757803047	snp	A/G	4.99438e-05	0.00499694	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616122	TAGTCTGCTCTTCAT[A/G]GGCTGAGAAAGTTAC	161436
rs757804032	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665681	GTAGGCAGAGTAGGG[A/G]AAGGGGCAAGGGGCA	161436
rs757809422	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88669500	CTGCCTCTTTAGGTC[A/G]GACCCTGACCATAAC	161436
rs757818122	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88731375	TTTCCAGTCTCATCC[A/G]TGTCCCTACAAAGGA	161436
rs757822882	snp	A/G			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88614992	TACATTAAATATGCA[A/G]TTCTTTCTTCCAGTT	161436
rs757828686	snp	A/G	0.000190785	0.00976505	intron-variant	EML5	GRCh38.p7	14:88621815	TAATTATACATATCT[A/G]TAGGGCATAGGGTAA	161436
rs757831652	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770374	AGTTTTACCTCTCAC[C/T]TTTTAAATTTTATAT	161436
rs757834744	snp	A/C	1.65622e-05	0.00287764	missense, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88626963	GTTTTACTCCCACTG[A/C]GACAAACTGGGTATC	161436
rs757857387	in-del	-/A	4.79921e-05	0.00489834	intron-variant	EML5	GRCh38.p7	14:88621091	GTTGTAACCTCTTTT[-/A]AAAAAAATTATCTGT	161436
rs757894610	snp	A/G	1.66244e-05	0.00288304	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694316	TCTTACCTGCTTTAC[A/G]CCAAAATTTCATGTG	161436
rs757910888	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713505	TAGTTAGAGCCACGA[C/T]CTTGCTCTTTCACCC	161436
rs757914696	snp	C/G	1.94158e-05	0.00311569	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618679	TATCTGCAGAGAAGT[C/G]CATTTGAATGACAAA	161436
rs757931189	snp	A/C	1.66123e-05	0.00288199	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626857	CCAAATGCAATAGCG[A/C]GCATGGTCTGCATCC	161436
rs757935551	in-del	-/AAG			intron-variant	EML5	GRCh38.p7	14:88640832	TAGCTTAACAAAAAA[-/AAG]AAGATCCCAATAAAC	161436
rs757936195	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88664436	TCCGTTTCTCTAATA[A/T]AGCTATACTAAATCA	161436
rs757939159	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88663322	AGTGGTTTGATTTTT[G/T]TATATGTATATACAT	161436
rs757989639	snp	A/G	7.22569e-05	0.00601026	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738885	TGTTATTACCTTTGT[A/G]TCCCTGGTCTGTTTC	161436
rs758000918	snp	C/T	1.76896e-05	0.00297397	intron-variant	EML5	GRCh38.p7	14:88706221	TTACTGAAGAATTAT[C/T]TGACAGGGAAACTGT	161436
rs758002777	in-del	-/CT			intron-variant	EML5	GRCh38.p7	14:88785461	AAATAGATAAACTCA[-/CT]CTGTAACCACAAAAA	161436
rs758016766	snp	C/T	1.66294e-05	0.00288347	intron-variant	EML5	GRCh38.p7	14:88739050	ATTTAACGACAAATA[C/T]TTTTTAAGAACATCT	161436
rs758024654	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633199	AAAAAACAAATACTT[C/T]GTTTTATTGCCATCA	161436
rs758033305	snp	C/T	1.65619e-05	0.00287762	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736407	CAGCCAAAGGTTTAG[C/T]AGGATGGACAGCAAG	161436
rs758055529	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88631258	TCACTCTGTCATCCA[C/G]GCTGGAGTGCCATGA	161436
rs758065194	snp	A/G	2.44939e-05	0.00349948	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657462	TAAGGCTCTGATGGT[A/G]TAACTGATTTCATTC	161436
rs758078887	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88686487	GGCGGACAGGGAGTT[A/G]GGCCTGATGCTGCCC	161436
rs758081637	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88711392	CAGTTCAGCATGGCT[G/T]GGGAGGCCTCAGGAA	161436
rs758082858	snp	C/G/T	4.97214e-05	0.00498585	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616820	GATACACAGGCACAG[C/G/T]TGACATCAGCTTTCT	161436
rs758108025	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88783646	ACGCACCCAACACTA[C/G]AGCACTTAGATATAT	161436
rs758138526	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88719625	TGTGTATATATAATT[A/T]TCTACTTTAAAATAT	161436
rs758138634	in-del	-/CCCCCGCT	0.000132179	0.00812847	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792290	GGGTGACGGCGGCGG[-/CCCCCGCT]CCCCGGTACCTGATG	161436
rs758139758	snp	C/T	3.31978e-05	0.00407404	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616213	ATTTGTCACATGGGG[C/T]GAATGACCCAAGAAC	161436
rs758147740	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88690326	ATTCTGACTTCTGGA[A/T]TGAGAATAGATACAA	161436
rs758148053	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88636418	CTGTAATCCCAGCAC[G/T]TTGGGAAGCCAAGGC	161436
rs758151240	snp	A/C	4.975e-05	0.00498724	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642975	ATAGTGAACATTATT[A/C]CTACAGTCTCTGCCT	161436
rs758163224	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784990	ACGTGGTATATATAC[A/G]CAATGGAGTACTAGT	161436
rs758172443	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653647	CCCAGGGATGAAGCC[A/G]ACTTGATTGTGGTGG	161436
rs758180644	snp	A/C	1.70292e-05	0.00291793	intron-variant	EML5	GRCh38.p7	14:88643064	TATTCTTCCTCATGT[A/C]TAAATGTTCACCACT	161436
rs758186033	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691337	GACAGTTTTCTCTCT[C/T]GTTCTATAATTACCT	161436
rs758194757	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88780936	TAAGATGTTAATCAT[-/G]ATCTATAAAATACCT	161436
rs758203290	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88637773	GAGATGGGCCTTGTT[C/G]CTTGTGCACAGTGAA	161436
rs758220016	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88775717	AAGCACACTGGCCTG[G/T]CCGGCTTTACCACCT	161436
rs758220907	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88726174	AACAACAACAACAAC[A/C]ACCCCATTTTAACAG	161436
rs758221208	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88708825	TATGAAAACTATGAT[-/A]AAAAAATGATTCAGT	161436
rs758233636	snp	C/G	1.67075e-05	0.00289023	intron-variant	EML5	GRCh38.p7	14:88664656	TTTGCTTGACATTTT[C/G]TATCTTTGGAAATAC	161436
rs758262250	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773854	CCGGGCATAGTGGCT[C/T]ATGCCTGTGATCCTA	161436
rs758262675	snp	A/C	5.36131e-05	0.00517723	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695395	CTCCTTTCTTCCAGT[A/C]CCAGAGCACAACAGT	161436
rs758272995	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88777213	AAAGAAACAACACAC[A/C]ACGGAGCTCCAATAC	161436
rs758274014	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88712746	GCAGGTTCAATTATG[C/T]GGAGAATAAAACTGA	161436
rs758282629	snp	A/G	3.23483e-05	0.00402158	intron-variant	EML5	GRCh38.p7	14:88726513	ACTGAAGATAAAATT[A/G]TTATGTGTTTCTACC	161436
rs758326101	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88623129	CAAGCGATTCTCCTA[A/C]CTCAGCCTCCCGAGT	161436
rs758329230	in-del	-/ACCA			intron-variant	EML5	GRCh38.p7	14:88706476	AATGCTAAACAAAAT[-/ACCA]TTTCAAACAATTTTT	161436
rs758330893	snp	C/T	2.09839e-05	0.00323906	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754655	CTACCAACACTCGTT[C/T]AGGATGCAATGCAAG	161436
rs758337305	in-del	-/AAAC			upstream-variant-2KB	EML5	GRCh38.p7	14:88794458	GCAGCTGCTGCAAAT[-/AAAC]AAAGAAATCAGGCCT	161436
rs758350034	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637891	TGGGTAATGTTCCAT[C/T]TACTTTTAAAAGTAG	161436
rs758358447	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727763	ATAGGTTATTTCTAC[C/T]CTGACCAAAGGGAGA	161436
rs758373267	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88624193	GTGATCCTCCCACCT[C/T]AGCCTCCTGAGTAGC	161436
rs758382046	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88662861	TCCTTTTATTAATAT[A/T]GTGTTTCTTCCTTCA	161436
rs758382507	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677260	GCCACATGCAGAAAA[C/T]TGAAGCTGGACCCCT	161436
rs758386364	snp	A/G	1.67346e-05	0.00289258	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754531	CCATCTAAGTCAAAC[A/G]CCAAGCAAGCTATAC	161436
rs758399611	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617168	TTTTTTTTTTTGAGA[C/T]GGAGTTTTCGCTCTT	161436
rs758427763	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768701	ACAGGCGTGAGACAT[C/T]GCACCTGGCCTATAA	161436
rs758429917	snp	C/T	3.60503e-05	0.00424545	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661676	GGATATCTAAATAAC[C/T]TCACAAATCCCAAAT	161436
rs758440859	snp	A/G	0.000103568	0.00719536	intron-variant	EML5	GRCh38.p7	14:88634516	AATAATTATCTATAA[A/G]TAACATAAATCTGTA	161436
rs758441495	snp	C/T	4.98931e-05	0.00499441	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746282	CCAACTGAAACCAAG[C/T]GCTGATTTATGTCCA	161436
rs758448261	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704256	AACCCCCTTCCCTTT[C/T]GATCCCTTTTTCCTT	161436
rs758467500	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88734632	ATCAATGGCTGCTAC[C/T]AGAAAAAACGGAGAC	161436
rs758473083	snp	C/T	1.68332e-05	0.00290109	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661797	AGCATAAACCAAGTA[C/T]ACTTGTCCATGATGC	161436
rs758474958	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88669187	GGATCAGGAGATCCC[C/G]TCCGTGAGCCCATGC	161436
rs758479075	snp	A/G	3.32364e-05	0.00407641	intron-variant	EML5	GRCh38.p7	14:88688245	GACAAATTTTGTTTA[A/G]TTTAAAATCTCTTTA	161436
rs758498830	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88682489	GAACATTTACTCAAG[A/C]AAATCTGTTAAAATT	161436
rs758522597	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88717650	ATCCCAGCTACTCAG[C/G]AGGCTGAGGCAGGAA	161436
rs758537029	snp	C/T	5.82971e-05	0.00539863	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88744032	TAGTACCTTGATATG[C/T]TTTACACCACAGCTG	161436
rs758538560	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88754420	CAAATAATTTTCATC[-/AA]GTGTCCAATTTAATA	161436
rs758539290	in-del	-/AC	1.69738e-05	0.00291317	intron-variant	EML5	GRCh38.p7	14:88685177	TGTTCTTTTAGACAT[-/AC]AGTTACTATAATACA	161436
rs758575543	snp	C/T	3.34857e-05	0.00409167	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618309	ACTTCATAGACATGC[C/T]GTTTATAGCAGCCAC	161436
rs758592624	snp	C/T	1.65858e-05	0.00287969	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625061	CTCTCGCCACGATTC[C/T]ACACAATATGTGATC	161436
rs758593368	in-del	-/TTG	2.06422e-05	0.00321258	intron-variant	EML5	GRCh38.p7	14:88696812	TGTTGCCTCTGCATT[-/TTG]TTAATTCTTACTGAG	161436
rs758626890	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88670772	AATGTTACAATGCAA[A/C]CACAAGTATCAATAA	161436
rs758630546	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756093	TCTAAGATGACTCGG[A/G]TTTCTGGCTTGGGTA	161436
rs758638671	in-del	-/TTGTGTTAAAAGAATATTCC			intron-variant	EML5	GRCh38.p7	14:88667336	GTTAACTTTACAATT[-/TTGTGTTAAAAGAATATTCC]TTGTGTTAAAAGAAT	161436
rs758646108	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88642692	TGAATTCCTTTTCTG[A/C]TGTATTATACTCTCT	161436
rs758669984	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705036	CTAATAAAGGTGTTC[A/G]TATACTCCCAATATA	161436
rs758670492	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88747115	AATAAGCTAAACAAA[C/G]AAACAAAAAAAAAAG	161436
rs758679844	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88655990	TGGAGAAGATGTGGA[C/G]AAACAGCAATGCTTT	161436
rs758692138	snp	A/G			utr-variant-3-prime, downstream-variant-500B	EML5, ZC3H14	GRCh38.p7	14:88614851	AGTGGCACACATCTA[A/G]ACAAATTTTCCCAAT	161436
rs758692532	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88787901	CTCAAACGGCTTGTG[C/T]TAAGAATTCTAGGCA	161436
rs758701151	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88671994	AACATTAGATCATAA[A/G]GACAGAAAATTAACA	161436
rs758715872	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88674381	GCCTCATGAAACTTA[A/C]AATCATAGCAGAAGG	161436
rs758735964	snp	C/T	0.000117583	0.00766665	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702481	CTTTCAAAGGATGAA[C/T]AGTTAGGCAGAGAAT	161436
rs758738796	snp	C/T	1.80553e-05	0.00300455	intron-variant	EML5	GRCh38.p7	14:88618204	CAAAGTCAGTTCTTG[C/T]CTTGTGAATATATAA	161436
rs758755203	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88741201	AAAAGTTGGGAATCG[G/T]TTAGCAATGAAAATG	161436
rs758763037	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794438	AAAAGAGGAATAGCT[C/T]TCTGGCAGCTGCTGC	161436
rs758767267	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660154	CAGGCATGGTGGCAT[A/G]TGCCTGTGGTCCCAG	161436
rs758787099	snp	A/G	3.36174e-05	0.0040997	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715065	CAACTTTTTTATAAC[A/G]CTGAGCAACTCCATA	161436
rs758820946	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88710590	TGGCCTAAGTGGTCT[A/G]CAAAACATAAAATCT	161436
rs758829753	snp	A/G	0.000175153	0.00935659	intron-variant	EML5	GRCh38.p7	14:88682063	GGATCAATTTAGTGT[A/G]TGTGTGTGTATATTT	161436
rs758831320	snp	C/T	0.000117117	0.00765144	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88649919	ACACTTACCTTACTA[C/T]TCCCTGCCTTCAAAA	161436
rs758835382	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88711279	GTTGAAGGAGAGACC[G/T]GGTGGGAGGTGATCG	161436
rs758850143	in-del	-/T	3.45331e-05	0.00415516	intron-variant	EML5	GRCh38.p7	14:88618345	ACCTTTTTCATCAGA[-/T]TAAAATGGGACAAGA	161436
rs758859721	in-del	-/A			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768514	TCCAGGGTTCAAGTG[-/A]ATTCTCCTGCCTCAG	161436
rs758885901	snp	A/G	1.73942e-05	0.00294903	intron-variant	EML5	GRCh38.p7	14:88681880	ACGTTCAAGTGTGAG[A/G]GCCTCTTACCCTTTT	161436
rs758885916	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88695284	TGCTTGATTTCAAAA[C/T]TCTTTTAATTAAAAA	161436
rs758901530	snp	C/G/T			intron-variant	EML5	GRCh38.p7	14:88747931	CTGTACAGAATACAT[C/G/T]AAACAAATGTTTTCA	161436
rs758901545	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88696983	AGAAGCTATTAAATA[C/G]AATTAAATTATTTAT	161436
rs758902605	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88707526	TACAATGATGCTTAG[C/T]TTCCTTTTGATATTG	161436
rs758904558	snp	A/G	1.66043e-05	0.00288129	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616196	CCACTGGTAAATCGA[A/G]TATTTGTCACATGGG	161436
rs758922261	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88733221	GACTATCCTCCTTTG[A/G]CAAATGCTGGGTCTT	161436
rs758930869	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88643237	ATACTTTTCTATATA[A/C]AGTTATGAAAAGGAA	161436
rs758955088	snp	A/T	1.65754e-05	0.00287879	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621171	GCAGAAAGGAAAAAA[A/T]CCCTGGAAGGATGTG	161436
rs758968634	in-del	-/AAAAAAAAAAAAAC			intron-variant	EML5	GRCh38.p7	14:88759698	TTAAAAAAAAAAAAA[-/AAAAAAAAAAAAAC]AAAAAACTGGGGAGA	161436
rs758973703	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88699115	GATGAAGGGGAGAAG[A/G]GAGAGGTTGGGAGAG	161436
rs758989019	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88776983	TTACTGGCCTTAAAG[A/G]GGAGCTAGATAAAGA	161436
rs758992884	snp	A/C	1.78401e-05	0.00298659	intron-variant	EML5	GRCh38.p7	14:88621395	TTGACCTGCTTTCAG[A/C]GAACTTTTTGCTTTG	161436
rs759023036	snp	C/G	3.40258e-05	0.00412453	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622587	GCTGCACTGTATCAG[C/G]TCATGGAACATCTTA	161436
rs759027054	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88650566	AACCAAATAGAATGG[C/T]TATTGTCATCAGAAG	161436
rs759039658	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88718807	TTAAGATGGGACACA[C/T]TGAGCATGTTCTAAT	161436
rs759043814	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88624088	TTTGTTTTTGTTTTT[A/G]TTTTTTAAATGGGGT	161436
rs759052660	in-del	-/TT	1.77087e-05	0.00297557	intron-variant	EML5	GRCh38.p7	14:88664460	TAAATCAAATGAAAC[-/TT]TTATCAAGTATTAAG	161436
rs759060704	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691127	ATCTCAGTCTAGTAG[C/T]TGCCCCATTTCTGGT	161436
rs759065664	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88790480	ATAACACAGCTTCTA[A/T]TTACTGCTAGAAGAA	161436
rs759087657	snp	A/G	8.28617e-05	0.00643615	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88685039	AAGTGTTATTGGGCC[A/G]CTTTTATCCACTTCT	161436
rs759105418	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647109	GTTTTTAGTTTATAA[C/T]CCCAGCACTTTGGGA	161436
rs759120592	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778285	AGAGAAAGTTCTTAC[C/T]TATCAATAACAATAA	161436
rs759122374	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88745938	ACTTAAAAGTATAAT[-/A]AAAAAAAAGAAAAAA	161436
rs759137493	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88745903	GTAACAAACCTGCAC[A/G]TTCTGCACATGTACC	161436
rs759140688	snp	G/T	1.72095e-05	0.00293333	intron-variant	EML5	GRCh38.p7	14:88682046	CCTATAAAGAAAACA[G/T]AGGATCAATTTAGTG	161436
rs759142619	snp	G/T	1.6563e-05	0.00287771	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702592	CAATTTCACCAATTT[G/T]AGTATAAAACAGATT	161436
rs759160241	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88639939	TGGTAGTAGTAACAG[C/T]GAAGAGACCTTGTAA	161436
rs759183910	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88679468	AGGCCAAGGTGGGCG[A/G]ATCACTTGAGGTCAG	161436
rs759195609	snp	A/T	3.83726e-05	0.00438005	intron-variant	EML5	GRCh38.p7	14:88627617	GTATTCTTGTTTTTT[A/T]AAAAATCAAACACAC	161436
rs759202776	snp	C/T	1.69596e-05	0.00291196	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702467	TGTTGCCACGTAGTC[C/T]TTCAAAGGATGAATA	161436
rs759203985	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88683227	ACCGTAGGCCAGCTA[G/T]TTTGTCCAAGAGAAC	161436
rs759238733	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717612	TACAAAAAATTAGCC[A/G]GGTGTGGTGGCATCC	161436
rs759243692	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678566	ATTAATTGTACTCAT[C/T]ATAGTACTAGCTTTC	161436
rs759249686	snp	A/C	2.02345e-05	0.0031807	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695365	TTTTTTCCTACCTTG[A/C]TATTGAAAGTTTCTC	161436
rs759250155	snp	A/C/T	3.46616e-05	0.00416291	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642902	TCCTACCTGTAGCAA[A/C/T]ATTGTGCAGAATTCC	161436
rs759252126	in-del	-/CAGTC	1.65611e-05	0.00287755	frameshift-variant, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688390	AAAAAGCCATCTCTT[-/CAGTC]CATCCATACACTGCA	161436
rs759259485	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88667457	CCAAGGGTAGCTGCA[A/T]CTCTTTGGGTAGAAA	161436
rs759264997	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88729309	TCTTCAATACTTCAA[A/C]ATTAAATATGATATT	161436
rs759277634	snp	C/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614655	ATTTTCAATCTTCAG[C/G]AAACTACAGATAGGC	161436
rs759281789	in-del	-/AAAG			intron-variant	EML5	GRCh38.p7	14:88750649	AGTTACAATTTCTGA[-/AAAG]AAAGTTTTACTATTT	161436
rs759289472	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88765905	CCGAACGGAGGGACC[A/G]GCTGAAGCCATGGCA	161436
rs759302017	snp	A/G	1.75133e-05	0.00295911	intron-variant	EML5	GRCh38.p7	14:88712267	ATTTTGAAAGAAAAG[A/G]TACCTTTTCTTAAAC	161436
rs759315073	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88735576	CAGGCACTGGTAATA[C/T]ATTCACAATAGGTGT	161436
rs759335087	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88670401	GTCCCTGCAAAAACC[C/T]CATCCAAAGTTCAGC	161436
rs759358014	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88789879	ATATTTGACCAATAA[C/G]TTTTACATAAGTTTC	161436
rs759379937	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88694611	CAAGAGACAGAAATG[A/G]TCAAAACTGAACTCC	161436
rs759382588	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769903	TAGTAGACACAAAGA[C/T]AGTTCAGAATTGGTA	161436
rs759426775	in-del	-/A	1.66219e-05	0.00288283	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616158	GCAGTCATCACCTCC[-/A]AGCACTAACAACATG	161436
rs759434040	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88630643	TCAGCACATGGTATT[A/C]CCCTAGTATCTTCTC	161436
rs759457182	snp	A/G			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615926	AGTTTAATATTTTTC[A/G]GTTGTGCTTTCAGGT	161436
rs759457830	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671501	ACTACATTAAGTGTG[C/T]AACATAACCAGCTAG	161436
rs759458142	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653524	GTGCTGAATTTTATC[A/G]AAGGCCTTTTCTGCA	161436
rs759502655	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88779442	AGTTTATATAATAAA[A/G]GCTAACAAGGGATAA	161436
rs759503475	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770931	TCCTATTAATATTGC[C/T]GAGTAATGGAAATTA	161436
rs759507183	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788455	TAACCTGCAACCATA[C/T]AGTGTGGTATACTTT	161436
rs759509325	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88756651	AGGTTGCAGGATATA[A/C]GATCAACATAAAAAA	161436
rs759511355	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654769	CTGTTGATTTGGGGT[A/G]GACAGTTCTGTAGAT	161436
rs759514313	in-del	-/AGG			intron-variant	EML5	GRCh38.p7	14:88688591	AGGCATGCAACAGTA[-/AGG]AGAATTGAAAACTAC	161436
rs759526926	snp	C/T	4.14791e-05	0.00455388	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705580	CACTATGAGAGTCAG[C/T]CAGACTTTCTGTAAT	161436
rs759546704	in-del	-/TACT			intron-variant	EML5	GRCh38.p7	14:88619469	CTTGGCCTCCCAAGG[-/TACT]GGGATTACAGGTGTG	161436
rs759555159	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88637183	TTAGTCTTCCCTTGA[C/G]TCTATCTTAATTAGT	161436
rs759562573	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758278	GCTTACTGCAACTTC[C/T]GCCTCCCAGGTTCAA	161436
rs759570025	in-del	-/TATATT			intron-variant	EML5	GRCh38.p7	14:88694820	AAAAGCATTTATCTA[-/TATATT]TAAAGTGCTTTAACA	161436
rs759577381	snp	G/T	1.68369e-05	0.0029014	intron-variant	EML5	GRCh38.p7	14:88658162	TTTCCCTATATTTTT[G/T]TTCAAGTATTATAAA	161436
rs759579683	snp	A/G	1.6607e-05	0.00288153	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616286	GCATTTGGTGCACAC[A/G]GAAGTCAAAGGCTCT	161436
rs759622384	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675517	CAGAGTAGAGGGGCC[C/T]GTGGCCTGGCCCACA	161436
rs759624876	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88722631	TGGGGTGAGGGGAGG[A/G]GGAGCATTAGGAAAA	161436
rs759630196	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88711244	CACCTAAATCTCATC[G/T]CGAATTGTAATCCTC	161436
rs759632461	snp	C/T	3.31746e-05	0.00407262	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625055	TGTGAGCTCTCGCCA[C/T]GATTCTACACAATAT	161436
rs759632850	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88762824	GTCTCTCAGACCACA[C/G]TGCAATCAAGTTAGA	161436
rs759652483	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713284	GTAATCTCAGCTACT[C/T]GGGAGGCTGAGGTAG	161436
rs759665263	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88646900	AAATATGGAAGATGA[C/G]AAAAATACAAAGTTA	161436
rs759677522	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88661535	AATTCTGAACCTTTC[A/C]TATTACAACATTACA	161436
rs759707510	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748967	ACATACAGGTAATCA[C/T]GGCTCTAGAAGGAGA	161436
rs759729873	snp	A/G	2.09721e-05	0.00323815	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615828	ATCTCTCAGTGAGGT[A/G]TATGTACACATTTCC	161436
rs759734774	snp	C/T	1.65877e-05	0.00287986	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644470	CCTACATTGTTTGTC[C/T]GGAGTTTCTCTGGCT	161436
rs759742988	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88782001	GGAGGGCTCAGAAGA[A/C]GATAGGAAAATGTGG	161436
rs759744505	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780795	GGCCAGAATGGTCTC[A/G]ATCTCTTGACCTCGT	161436
rs759762445	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750390	TGCTTCATATCATTA[C/T]TATTATTGCTATTAG	161436
rs759812422	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88755615	TCAATTTACAATATC[A/C]TATTTGCCCTTGAGA	161436
rs759832983	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88644249	TAAAAGGAAGACTAA[C/T]TTAAAAAATTAAGAG	161436
rs759838252	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88703131	CTAAATCTAAGCTAT[A/C]ATACTGAGTGAAAAA	161436
rs759849264	snp	A/G	0.000116747	0.00763938	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792312	TCCCCGGTACCTGAT[A/G]ATGTCGTCGCTGTGG	161436
rs759864416	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88740709	TGATAAAATAGCATT[C/T]AATGTTCAGATTCTC	161436
rs759871007	snp	C/T	2.12565e-05	0.00326003	intron-variant	EML5	GRCh38.p7	14:88663016	ACAACACTGCAAGCA[C/T]CACTGTTGTCCTACC	161436
rs759884259	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88629140	CAGTGATAAATATTA[C/T]ATAAATATTTTTATA	161436
rs759887516	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88627153	ACAAAGGCTTAGAAG[A/G]GAGGCCAATGGCCCC	161436
rs759890677	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88774014	GTCCCAGCTACTTGA[C/G]AGGCTGAGGCAAGAT	161436
rs759895572	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88724748	GAATATTAATTATTA[G/T]TCATAAGTAATGACC	161436
rs759900762	snp	C/T	1.65614e-05	0.00287757	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688341	ACAAGAAAGATGTCT[C/T]TCCAGATACACACAT	161436
rs759909036	snp	C/T	6.37044e-05	0.00564342	intron-variant	EML5	GRCh38.p7	14:88744013	TTATAAAACAAGACC[C/T]TTCTAGTACCTTGAT	161436
rs759934837	snp	C/T	1.67116e-05	0.0028906	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715054	CAAACACTCGCCAAC[C/T]TTTTTATAACGCTGA	161436
rs759943009	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88739186	TCCATAAGAACTTAA[C/T]ACAGTTGCCCCTTGT	161436
rs759956373	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88635685	TGTCTCATTCTCTTC[C/T]ATCCCACACCACAAA	161436
rs759967101	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619202	GAAACCCTGTCTCTA[C/T]TAAAAATACAAAATT	161436
rs759967343	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88634193	TAAACGTGTAGTACC[A/T]CCCCTTTCTCTCTCT	161436
rs759973428	snp	C/T	3.31373e-05	0.00407032	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688470	CTTCCAATCAATCCT[C/T]CCCCTAGTTCACAAA	161436
rs759992330	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88650897	TCCTCCCACTTCAGC[A/C]TCCCAAAGCACTGAG	161436
rs760000856	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88786314	TATAAAAATTTACAC[A/T]CATATATAAAATTTA	161436
rs760011614	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88620588	TTATAATTTAGCAAG[A/G]AGAATTAAGTAGTAT	161436
rs760018065	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88689905	ATATACTGTGCTAGA[C/T]GATGATGGGTGCTTT	161436
rs760029093	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88722285	ACACAAAGAAATATA[A/G]ATCATTCTATTACAA	161436
rs760047999	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88718254	GGATATGCATAGCTC[A/G]AGTTTTGAGATAACA	161436
rs760068564	snp	C/T			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615637	ATGGATTACGGATTA[C/T]ACCCAGTGCATATAG	161436
rs760102782	snp	A/G	2.13199e-05	0.00326489	intron-variant	EML5	GRCh38.p7	14:88618607	ACACGAAATGTAAAA[A/G]CAGAAGAACTTGCCA	161436
rs760109371	snp	A/G	4.32012e-05	0.00464744	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638848	TGATAAATTTGGGGT[A/G]CTGGTTTACTGTGAG	161436
rs760126982	in-del	-/CGAGC			upstream-variant-2KB	EML5	GRCh38.p7	14:88792946	CACCCCGAAACCGAG[-/CGAGC]CGAGCCGAGCCGAGC	161436
rs760140759	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88670098	GAGGCAGGTGGATCA[C/T]GTGGTCAGGGGTTCA	161436
rs760145751	in-del	-/ACAGTACAAGGCTGAAGATTCC	8.25048e-05	0.00642228	intron-variant	EML5	GRCh38.p7	14:88638945	AAGTTTGAAAATTTT[-/ACAGTACAAGGCTGAAGATTCC]AAGATGTAACAGCCA	161436
rs760149939	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88723224	TTGAGACAAGCCTGG[A/G]CAACACAGTGAGGCC	161436
rs760188556	snp	A/G	1.66818e-05	0.00288802	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618299	TCCTGAAGGCACTTC[A/G]TAGACATGCCGTTTA	161436
rs760190700	snp	C/T	1.71284e-05	0.00292642	intron-variant	EML5	GRCh38.p7	14:88625169	CAAACTCATCAAAAG[C/T]TCAAATAGAGTTTAA	161436
rs760193011	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88704606	TACTCTAAGTCAAAT[A/G]TGCCCAGTTGTCCCA	161436
rs760206699	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88743138	AAGGCTGAGAGAGGG[A/G]CAAGGAGAGATTTGT	161436
rs760227972	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88673230	TGCTAGGCTTGTTCA[A/C]CACACACAAATCAAT	161436
rs760228920	snp	C/T	1.72561e-05	0.0029373	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702455	ACCTACCTGGCCTGT[C/T]GCCACGTAGTCTTTC	161436
rs760230310	snp	A/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715154	TTTAACTCATGAATT[A/G]CCTCCTTCCTATCTT	161436
rs760236282	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637073	ACATTGTAAATGCTG[C/T]TTTGTGTTTTGTGGG	161436
rs760273567	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88742236	GACCAATAGAAATTT[C/T]AGTGATGATGAAAAT	161436
rs760289432	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88700912	CATAATGCATTCTAA[G/T]ATTTGAACACTGTGA	161436
rs760292906	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769749	TCTGTATCTAAGTAT[C/T]TGAAAATCATGAATT	161436
rs760303504	snp	C/T	1.67584e-05	0.00289464	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661752	CAGTTACATCTGTAA[C/T]TTCTCCAATTACTGG	161436
rs760311553	snp	A/G	1.66358e-05	0.00288402	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715034	GTGATGAAACTAAGG[A/G]ATCCCAAACACTCGC	161436
rs760312731	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788352	TTCTTAAGAACACGA[C/T]TTACCACAAATAAAG	161436
rs760317575	snp	C/T	0.000746965	0.0193113	intron-variant	EML5	GRCh38.p7	14:88705828	TGGCTCCCCAATGAC[C/T]GCTACATCAAATTTA	161436
rs760326689	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88744280	ATAAGAAATAAAAAG[C/G]ATTTCTTCATTTCTA	161436
rs760352512	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88759645	GCTGTGATCATGCCA[C/G]TATACTCCAGTCTGA	161436
rs760359249	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88780333	ATATTTGTATAGCAA[-/AC]AGACTTGAAAAATAA	161436
rs760362221	snp	A/C	1.66974e-05	0.00288936	intron-variant	EML5	GRCh38.p7	14:88746169	CTCATTAGAAATCTC[A/C]AAAGAGAATACTTAC	161436
rs760364509	snp	C/T	1.6869e-05	0.00290417	intron-variant	EML5	GRCh38.p7	14:88714933	TAATTTGCTAGAAAT[C/T]GTTACCTGGCATTCT	161436
rs760372540	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690841	CACAAATGGAAGAAC[C/T]GGCCTTTATTAGAGG	161436
rs760375207	snp	C/G	1.67556e-05	0.0028944	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706328	ACTGAAAGACAGAGT[C/G]ATCTGCTCCACCAAT	161436
rs760385600	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733034	GTAATGTGAAACTTA[C/T]ATTGTGGTAAAGTCA	161436
rs760397519	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88718546	AAGAGAATCAAATAC[G/T]GCTGGAAATTCAAGC	161436
rs760419925	snp	A/G	1.65941e-05	0.00288041	intron-variant	EML5	GRCh38.p7	14:88685009	CAAATTAGCATTTAA[A/G]ATTACCTGAACCAGA	161436
rs760421045	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638638	ACCAGAGTGAGTGAG[A/G]GAAAGGTACCTGAAA	161436
rs760435585	snp	A/T	0.000106197	0.00728608	intron-variant	EML5	GRCh38.p7	14:88627902	GCATATTCATCTGTG[A/T]AACATGGACAAATGT	161436
rs760436559	snp	C/T	6.99505e-05	0.00591357	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738993	AGCCTTCTTCACAAG[C/T]ATTCATGCTAAAAAT	161436
rs760442972	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88657552	ATAACTGAGATCAAT[C/T]ATGATCTTATAAATT	161436
rs760447346	snp	A/G	1.86128e-05	0.00305058	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626808	TGTAAAGTAGTCAAA[A/G]TCACACTATGTGCAT	161436
rs760450441	snp	G/T	5.02609e-05	0.00501278	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88622714	CCGCTCCTCCTTCTT[G/T]TGACCTAAGTAAATA	161436
rs760455698	in-del	-/CTC	1.65894e-05	0.00288	cds-indel, nc-transcript-variant	EML5	GRCh38.p7	14:88616869	TTCCCAAAACCTCAT[-/CTC]CTAGAATACTAGAGG	161436
rs760459431	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88748590	AAAATTACAGGTATG[G/T]GAAGAAACAGGAAAA	161436
rs760498097	snp	C/T	0.000168912	0.00918844	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657414	TTGTTGTAAATGAGG[C/T]TTGATTCCTAACATT	161436
rs760528994	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681904	CCCTTTTTCAGCTTC[C/T]GGACAGCCAACATAC	161436
rs760572218	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88734343	AATGTAAGTATTAGA[A/C]TGCCACCATTTGAAA	161436
rs760582086	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88682887	AGGGCCTAAAGCCTG[A/T]GATACTCAAAGATAA	161436
rs760587567	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769485	ATCCAGTCTCAGGTA[C/T]TTCTTTATAGCAGTG	161436
rs760601501	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88619057	AATTCCTTTAAAAAC[A/G]TCTAATGGCTTAAAA	161436
rs760607238	snp	A/T	1.70697e-05	0.00292139	intron-variant	EML5	GRCh38.p7	14:88682035	TTCCATGTGTCCCTA[A/T]AAAGAAAACATAGGA	161436
rs760608315	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674585	ACATGTGAATTCGAG[A/G]TGAGATTTGGGTGGG	161436
rs760621555	snp	A/G	1.73171e-05	0.00294249	intron-variant	EML5	GRCh38.p7	14:88738858	GTTTGCCTAGTAATA[A/G]GACATTTGTTTTGTT	161436
rs760621633	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768367	TTAGCAACTATTGGC[A/G]GATTCTGTCAGTAAC	161436
rs760658629	snp	A/C			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615667	GCAAATATTTTGAAC[A/C]GATCAGTCTTTCACT	161436
rs760674698	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755820	AAACACAGCAAACCA[C/T]TGTCTCTACAAAAAA	161436
rs760679438	in-del	-/TC			intron-variant	EML5	GRCh38.p7	14:88748239	ATGAACTCTATGAGG[-/TC]TCATGCAAAGAAGAA	161436
rs760714914	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760461	TTTTGTCAAAAATCA[A/G]TTGACCATATCTATA	161436
rs760722847	snp	A/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614460	TATTAACCAAGTATT[A/G]GACACAGAAAATAGG	161436
rs760733165	snp	C/T	8.30889e-05	0.00644496	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704912	CCCGCTCTCTTCTTT[C/T]AGAAGTAGCACTTTT	161436
rs760760860	snp	G/T	7.47058e-05	0.00611125	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615891	GCAGGGAGTTAATTA[G/T]GTTTTTAGATTTTCA	161436
rs760760999	snp	C/T	1.7501e-05	0.00295807	intron-variant	EML5	GRCh38.p7	14:88621381	TAAAAATGACCCTAT[C/T]GACCTGCTTTCAGAG	161436
rs760816061	snp	C/T	1.65976e-05	0.00288072	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644456	GTCTCTTTTTCTTGC[C/T]TACATTGTTTGTCTG	161436
rs760822012	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747618	GCGAAATAAAATTAA[A/G]GATTCAAAATATCTG	161436
rs760824599	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721837	AAAGAGGCAACCTAC[A/G]GAGTGGGAAAAAATA	161436
rs760841279	snp	C/G	1.81394e-05	0.00301154	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665374	AATCATATCTTTTCT[C/G]TGATGAAAAGACACA	161436
rs760847483	snp	C/T	1.65825e-05	0.00287941	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726604	TGGATTCCATCTGCA[C/T]TGACAGCTGCACAAC	161436
rs760880346	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88693164	TGTCTTTAACAGAAG[-/A]AAAAGTCTGGACATA	161436
rs760896386	snp	A/G	2.23297e-05	0.00334131	intron-variant	EML5	GRCh38.p7	14:88695476	AAAATTAATGAGAGA[A/G]ATAAACTGACTATTA	161436
rs760915644	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766863	ATTTCTCAGACTGGC[C/T]GACACTTAGGGAAAA	161436
rs760922444	snp	A/C/G	5.00591e-05	0.00500275	intron-variant	EML5	GRCh38.p7	14:88664648	GAAACATATTTGCTT[A/C/G]ACATTTTCTATCTTT	161436
rs760945377	snp	A/T			missense, intron-variant, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88634475	TTTCCTTACCTGACA[A/T]GTCTGCTGAATCACC	161436
rs760956231	snp	G/T	0.000121146	0.00778192	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88620765	TAACCTGATATCATG[G/T]ATTGCACATCTCCTG	161436
rs760962151	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700164	TAGTACAATTAGTCA[C/T]GTTATTCGACTTTCC	161436
rs760967063	snp	C/G/T	3.3278e-05	0.00407898	intron-variant	EML5	GRCh38.p7	14:88616918	ACTCATCATGGCAAG[C/G/T]GCGGGCAGGTTGACT	161436
rs760969665	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660022	GACTCGCGCCTGTAA[C/T]CCCACCACTTTAGGA	161436
rs760972426	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88714437	TATAAGTTTCAGTTA[C/T]ACAGGATGAATAAAT	161436
rs760987239	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88694504	GATTACTCTATTTAC[A/G]AATATTTTACTCCCA	161436
rs761022605	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88784901	ACACTCCAATGTTTG[C/T]TGCAGCACTGTTCAC	161436
rs761065080	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88665643	ACCAGCCCGGGCAAC[A/C]TAGCAAGACCCCATC	161436
rs761071089	snp	G/T	1.66963e-05	0.00288927	intron-variant	EML5	GRCh38.p7	14:88658405	TAAAGAGGAAGAAAA[G/T]TCAAACAATCTTTCT	161436
rs761071396	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88752744	CCTTTGCCAAAATCA[C/T]TCTGGCCCACAACCC	161436
rs761079149	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721967	AGGACATGAGCGGAC[A/G]CTTTTTGAAAGACAA	161436
rs761084112	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88649049	CACCCCCCACCCCCG[A/T]AACAGGGTCTTGCTG	161436
rs761085139	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701241	GTGGGTGTTCCTGGC[C/T]TCTAATGGGTTGAGA	161436
rs761107717	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88775559	AAGAGTGGGAAGGAC[A/T]GCGCCTTGTGGTTTG	161436
rs761126771	snp	A/G	5.12904e-05	0.00506385	intron-variant	EML5	GRCh38.p7	14:88622751	CCAGAGTAAGTGTTC[A/G]TTATTGGCTACTATA	161436
rs761128560	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88750278	ACCTATTAAATGGGG[A/G]TATAAAATTACTTCA	161436
rs761136340	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88721322	AAGTCAATCCTAAGC[-/A]AAAAGAACAAGGCAG	161436
rs761143691	snp	A/T	1.65883e-05	0.00287991	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625044	CACAGGCCCGTTGTG[A/T]GCTCTCGCCACGATT	161436
rs761218019	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88634001	AATCCGCAAGTTTTT[A/T]ATAGAGTAACAAGAT	161436
rs761229887	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772837	TACACTCCAGCTACA[C/T]TGGCCTTTCTATCCC	161436
rs761233078	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88668701	TTTACTCAATGCTTA[G/T]TCTGCTGGTTGGGTG	161436
rs761241119	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88697980	GACCTCAGGTGATCT[C/G]CCTGCCTCGGCCTCC	161436
rs761242009	in-del	-/C	1.68781e-05	0.00290495	intron-variant	EML5	GRCh38.p7	14:88684970	ATATATTGAAATAAT[-/C]AATTGTATGTAAAGA	161436
rs761263649	snp	C/T	1.66131e-05	0.00288206	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658379	ACCTCTTAAACTTTC[C/T]AAATTTCCCCTAAAG	161436
rs761272631	snp	C/T	3.28132e-05	0.00405038	intron-variant	EML5	GRCh38.p7	14:88739048	TAATTTAACGACAAA[C/T]ATTTTTTAAGAACAT	161436
rs761276248	snp	C/T	1.66818e-05	0.00288802	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712388	TGATATCTGAATACT[C/T]GGGCCAAATTCCATT	161436
rs761290629	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88703272	AAAGTATATTTGTAT[G/T]TGTTGTATAAGTATT	161436
rs761297113	in-del	-/AAAAAAGA	1.69645e-05	0.00291238	intron-variant	EML5	GRCh38.p7	14:88694286	AAAATTCTATGGAGT[-/AAAAAAGA]AGCACTTTCTTACCT	161436
rs761297932	in-del	-/CTCACT			intron-variant	EML5	GRCh38.p7	14:88638614	GATTGTCAAGACCAA[-/CTCACT]CTCAGATAACCAGAG	161436
rs761307687	snp	G/T	0.000188871	0.00971597	intron-variant	EML5	GRCh38.p7	14:88696801	AAAATGCTATGTGTT[G/T]CCTCTGCATTTTGTT	161436
rs761310171	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786101	GGCATTTGCATTTGA[C/T]AGTCCCTTTACTTAA	161436
rs761315169	snp	A/G	2.56644e-05	0.00358211	intron-variant	EML5	GRCh38.p7	14:88687339	ACCCCTATGGAAAAA[A/G]AAAGGTTCAAGTTAA	161436
rs761331574	snp	A/G	1.70116e-05	0.00291642	intron-variant	EML5	GRCh38.p7	14:88644550	GGAAAGGCATGCAGC[A/G]CTCAGTGCCTTCACT	161436
rs761343270	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700609	TTACTGCAAACCCAT[C/T]ACTCCACTACAACAA	161436
rs761343635	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88688652	ACCTTGCATAACTGC[A/G]TTTAGACCATAACTT	161436
rs761381720	snp	A/G	3.45036e-05	0.00415338	intron-variant	EML5	GRCh38.p7	14:88714913	GTATAGGTACTACAA[A/G]TCTATAATTTGCTAG	161436
rs761387936	in-del	-/CA			intron-variant	EML5	GRCh38.p7	14:88665129	CATCCTGGCTCAAGT[-/CA]CACAGAAAATTTAGT	161436
rs761388951	snp	A/G	8.20378e-05	0.00640408	intron-variant	EML5	GRCh38.p7	14:88627862	TAATCTACCTGTTAT[A/G]AATATTTCTGTTTCT	161436
rs761395673	snp	A/T			utr-variant-3-prime, downstream-variant-500B	ZC3H14, EML5	GRCh38.p7	14:88614095	CTGTAATGGAAATAT[A/T]ATTTCTCTGTAGCCA	161436
rs761403275	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755723	CAAGGCTGGGTGTAG[C/T]GGCTCATGCCTATAA	161436
rs761432121	snp	C/T	1.66849e-05	0.00288828	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618247	TCCATGTAGCCCAAG[C/T]AATTCTGTCAATAGC	161436
rs761443862	snp	C/T	2.11013e-05	0.00324811	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615841	GTGTATGTACACATT[C/T]CCAGACAAATAAGCT	161436
rs761450754	in-del	-/AAC			intron-variant	EML5	GRCh38.p7	14:88717762	CCGTCTCAAAACAAC[-/AAC]AACAACAACAACAAC	161436
rs761456705	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756448	AGTAAAGGGAAAAAA[C/T]AAGGATGTCAGTTCT	161436
rs761459280	snp	A/G	6.98641e-05	0.00590992	intron-variant	EML5	GRCh38.p7	14:88743977	AATATATACTTAGCA[A/G]CAGAGAACTAAACGT	161436
rs761459934	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612498	GAAACTACATTATCA[C/T]AAAATTATACAAATT	161436
rs761483664	in-del	-/AAAG	0.000206101	0.0101493	intron-variant	EML5	GRCh38.p7	14:88620949	TAAAAAAAAAAAAAA[-/AAAG]AGTCATAGGAAACAT	161436
rs761507281	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88746735	GTGGGCTGAGGAAGA[C/T]AGGAGACAAAGTCTA	161436
rs761519632	snp	A/C/G	1.6703e-05	0.00288985	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740542	AGACACCTCGTTTTG[A/C/G]GGTCAGAGCATTTCC	161436
rs761530690	snp	C/T			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621140	ATCCCAAAGTCTCAC[C/T]GTCCCATCTTCTGCA	161436
rs761538705	in-del	-/T	5.85349e-05	0.00540962	intron-variant	EML5	GRCh38.p7	14:88627610	ACCTTTGTATTCTTG[-/T]TTTTTTTAAAAATCA	161436
rs761542263	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88651017	CAATTATTTAAATAA[A/G]CCATGAACCATATTA	161436
rs761542688	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710045	GAGGTGATGGGCTAA[C/T]GTAACTCTGCCCTCA	161436
rs761543683	snp	A/C	1.81e-05	0.00300827	intron-variant	EML5	GRCh38.p7	14:88702433	TGGCTTATTGTCAGT[A/C]TTTCAAACCTACCTG	161436
rs761545020	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88716436	ATTAAATCCATATAC[C/T]GTATTGCCCTTTGCT	161436
rs761553639	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704525	AGAGACACAGAGAGG[C/T]TAAGTGACTTGTTTA	161436
rs761569434	snp	C/G	1.70017e-05	0.00291558	intron-variant	EML5	GRCh38.p7	14:88646938	TAAACACAGCAAAGA[C/G]AGGATTACCTGGAAC	161436
rs761571434	snp	A/G	1.658e-05	0.00287919	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681967	GTTTTATCATCGCTT[A/G]CAGTAGCACAGATGG	161436
rs761599528	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88636104	AGAACTCCATCCACC[C/G]CTACACAAAGAACAG	161436
rs761606174	in-del	-/AC			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615714	GCATTTCTCCCTGTT[-/AC]AGTCTTGGGTTAGCA	161436
rs761622402	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783157	GTATGTTGCAGGGGC[A/G]GAGCCCTCATGGAGA	161436
rs761624619	snp	A/G	5.03309e-05	0.00501627	intron-variant	EML5	GRCh38.p7	14:88665532	TTTTCCCTTTTTTCT[A/G]ATTTAAAGTATGGGC	161436
rs761646321	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88646480	CCATTTCAAAGAATG[A/T]TAGAAGCCTTGCTTT	161436
rs761663802	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761725	CCAGTAATGGGATTC[C/T]TGGGTCAAACGGTAT	161436
rs761678123	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659663	CCTATTCCTAAGGGA[C/T]CTACACCATCTGGAA	161436
rs761704399	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88696335	CCGTAGATCTATCTG[C/T]AGTGGTCAAACTTTT	161436
rs761706254	in-del	-/CAAA			intron-variant	EML5	GRCh38.p7	14:88726107	ATTTTTCTAATTACT[-/CAAA]CAAAAGAAGAGATGG	161436
rs761714991	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747581	AATAACATAAGCTTA[A/G]CGTGAGAAATAAGCT	161436
rs761720203	snp	C/T	1.65616e-05	0.00287759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621220	GCCCATCCACATGAC[C/T]GTTAACTAAAATATT	161436
rs761730056	snp	A/G	4.53741e-05	0.00476288	intron-variant	EML5	GRCh38.p7	14:88620740	TAGAAACTCTATTCC[A/G]TTTGTTCACTAACCT	161436
rs761745839	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779326	TATAGCACAGAAATA[C/T]AGATTTACTCAACAG	161436
rs761763917	snp	A/C	9.71581e-05	0.00696919	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792369	CCGCGGGCTGTACAC[A/C]ACGCCGACCCCCGCC	161436
rs761774935	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88729825	CTCAGTCTCCCAAAG[C/T]ACTGGGATTACAGGC	161436
rs761776240	snp	A/G			intron-variant, synonymous-codon	EML5	GRCh38.p7	14:88680535	GTGGTTCTCGATGGT[A/G]GCACCCCAGACACCT	161436
rs761787213	snp	C/T	1.86277e-05	0.0030518	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754622	AAATATAAGGCTCTT[C/T]CCCAACTTGTCCTGT	161436
rs761792677	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88734896	AGACTGAAAAGACAT[-/A]ATCAGCAAACGCAAT	161436
rs761809174	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88642208	TTTACTTCTAACTTT[A/C]AGACTTTTATGAAGT	161436
rs761864095	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641182	ATTCTCCCAGACATA[C/T]AAAGAAAAGCTGGTG	161436
rs761869522	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88732860	CTGTTTCCCAGGCTG[C/G]AGTGCAGTGGCGCGA	161436
rs761872299	snp	A/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767159	GCAGACAAGCAATCC[A/T]ATTAGGTTCAAGGTA	161436
rs761877696	snp	A/C/G	0.000105635	0.00726693	intron-variant	EML5	GRCh38.p7	14:88621098	ACCTCTTTTAAAAAA[A/C/G]TTATCTGTACTTACT	161436
rs761892941	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701166	AACAGGGTGATTTTG[C/T]CTTCCAAGGGACATC	161436
rs761893856	in-del	-/AATA			intron-variant	EML5	GRCh38.p7	14:88672890	TGAAATTTAGGCAGT[-/AATA]AATAGTCTACCAACC	161436
rs761912191	snp	C/T	6.52805e-05	0.00571279	splice-donor-variant, intron-variant	EML5	GRCh38.p7	14:88638808	AAATACAGAAACATA[C/T]CTACTTGGCCAGTTG	161436
rs761920709	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88630845	CCACAAATGCAACCA[C/G]CCTTATCGGTGAAGC	161436
rs761937854	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88737294	TGGGGCTTCAGGGCC[A/G]CTAGAGTCCCCAAGT	161436
rs761952664	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760273	TTCTAAAACTTTTAT[A/G]GTTTGTCTTACATTT	161436
rs761953440	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633902	AGGTGTGAGCTACCA[C/T]GCTTGTCCAAAAAAA	161436
rs761957269	snp	C/T	1.66217e-05	0.0028828	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664581	TACATTGTATATATC[C/T]ATAAAGCTGTCATGG	161436
rs761959398	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88761646	ATTGTGAACAGTGCT[A/G]TAATAAACATACATG	161436
rs761974613	snp	A/C	3.86332e-05	0.00439489	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618794	ACCTACTGCCAGATA[A/C]CGGGAATCCGGACTA	161436
rs761975177	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721594	ACTGGACCCCTTCCT[C/T]ACACCTTATACAAAA	161436
rs761994250	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88637475	AATAAGTTGCCTAAC[-/AG]AGGGAGAGCAAAGGA	161436
rs761995778	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88618997	GAAATAAGGAAGCTT[C/T]ATATTTTACTTAAAT	161436
rs762006573	in-del	-/CTTT			intron-variant	EML5	GRCh38.p7	14:88757847	CTCTCTCTTTCTCTC[-/CTTT]CTTTCTATTTATTTA	161436
rs762008293	snp	A/G	2.8666e-05	0.00378579	intron-variant	EML5	GRCh38.p7	14:88695343	TTTTGCAAATGTGAT[A/G]TCAAGTTTTTTTCCT	161436
rs762010229	snp	A/C	9.69603e-05	0.00696209	intron-variant	EML5	GRCh38.p7	14:88663123	GTAAAAGCTTTCCTT[A/C]AAAAAAATTTTTAAA	161436
rs762012764	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88691874	TATGCTTCACTTTCA[A/G]GTCTACTATACGTCT	161436
rs762015860	in-del	-/TGAATAAATAATATAA	2.55353e-05	0.00357309	intron-variant	EML5	GRCh38.p7	14:88695495	ACTGACTATTAACAT[-/TGAATAAATAATATAA]TCAGAAGAGAGAAAA	161436
rs762029616	snp	C/T	1.93868e-05	0.00311336	intron-variant	EML5	GRCh38.p7	14:88712229	GAACACGAAAGTCTT[C/T]TGTGAGAGAGAGGTT	161436
rs762029995	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617611	CCTATCTCTACAAAA[A/G]TAAAAATGACTTATG	161436
rs762054862	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778183	AATCATATCACCAGA[A/G]AACATCACCTTAACT	161436
rs762060171	snp	C/T	3.31323e-05	0.00407002	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626918	TTTTGCTAAGAAGAG[C/T]TCTTCCTGCCAGGGT	161436
rs762060178	in-del	-/TTCAGTTT			intron-variant	EML5	GRCh38.p7	14:88751559	CGAATAAAGAGAGAA[-/TTCAGTTT]TAAATGTAGAAAATG	161436
rs762103626	snp	A/G	1.6582e-05	0.00287936	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616801	AAGACTGATTCCTGA[A/G]TGAGATACACAGGCA	161436
rs762113920	snp	C/T	0.000365667	0.0135167	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622644	CAATCTGTGGCTTGT[C/T]CTGTCTCAAGCCTGA	161436
rs762120554	in-del	-/T	2.49741e-05	0.00353361	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615891	GCAGGGAGTTAATTA[-/T]GTTTTTAGATTTTCA	161436
rs762127732	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88679652	AGCCAAGATCATGCC[A/G]CTGCACTCCAGCCTG	161436
rs762128225	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88713225	GGTAAAACTCCATCT[C/G]TACTAAAAATACAAA	161436
rs762137552	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88689828	TATGAACAGAACAGG[C/G]AAGACAACAAAATTC	161436
rs762162498	snp	A/G	2.63981e-05	0.00363295	intron-variant	EML5	GRCh38.p7	14:88705028	AATATATACTAATAA[A/G]GGTGTTCGTATACTC	161436
rs762166994	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88664104	GCAATATAGTGAGAA[C/G]CTGTCTGTACAAAAC	161436
rs762176566	snp	A/G	1.69421e-05	0.00291046	intron-variant	EML5	GRCh38.p7	14:88622741	AATAACCAAGCCAGA[A/G]TAAGTGTTCATTATT	161436
rs762184785	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88676964	GACTGACGTGCAGTG[C/G]CACAATCTTGGCTCA	161436
rs762187191	snp	C/T	0.000116369	0.00762699	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704899	CTATTTCCTGGAGCC[C/T]GCTCTCTTCTTTTAG	161436
rs762205041	snp	C/T	2.65059e-05	0.00364036	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687223	CAAATCACCTTTAGA[C/T]CCTGGGGCCAATGCA	161436
rs762210299	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665596	CTCTGGGGAGCTGAG[A/G]CAGGAGGACTGCCCG	161436
rs762239142	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764531	AGTTTATCAATCTGA[C/T]CCTTTTCAAAGAACC	161436
rs762242210	snp	C/T	3.57417e-05	0.00422724	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726595	AGGGCAAGATGGATT[C/T]CATCTGCATTGACAG	161436
rs762245963	snp	C/T	1.66732e-05	0.00288727	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644433	GTGAGTTTTCCTTAC[C/T]TCTATAGGTCTCTTT	161436
rs762287867	snp	A/T	8.39215e-05	0.00647717	intron-variant	EML5	GRCh38.p7	14:88643038	CTATAATGATAATAA[A/T]AAAACCATTATATTC	161436
rs762324877	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88693546	ATTACAAGTGAAGGT[A/G]AGATTTGGGTGGGGA	161436
rs762344389	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647346	GCACTGCAGCCTGGG[C/T]GACAGAGCACGACTC	161436
rs762355260	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88729610	TTTGTCACCCAGGCT[A/G]TAGTGCTGGCGCAAT	161436
rs762359710	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88750754	CAAATCAAGCTAGCA[A/G]AAAGCCCAGAGAACA	161436
rs762361852	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765681	ATTCACAGGTTCCAG[A/G]AATTAGAGTATGGAT	161436
rs762377305	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88783242	AATGTGGGGTTGGAT[A/C]CCCTACACAGCTTCA	161436
rs762377653	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88679899	GTATAGTGTAGCGTA[C/T]AGTAAGGGCCTTTTA	161436
rs762379412	snp	A/G	6.64397e-05	0.00576328	intron-variant	EML5	GRCh38.p7	14:88616891	AATACTAGAGGGAAG[A/G]AACAAAAGAAAACTC	161436
rs762406475	snp	A/G	1.67156e-05	0.00289093	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740417	TATTGTTCGTATAAG[A/G]TTGATTCCTTTCCAA	161436
rs762408479	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88714728	CCAAAAGGATTTCAA[C/T]ATAAGGCAGCCTTAT	161436
rs762413268	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752442	TCTGACAGAACATTA[A/G]GACTTGAAAAATAAT	161436
rs762440703	snp	A/G	5.04206e-05	0.00502073	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712293	TAAACATGGATATCG[A/G]AATAATTTTATAATT	161436
rs762453622	snp	A/G	1.66496e-05	0.00288522	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88704879	GAACAAAGTGTAATC[A/G]AATACTATTTCCTGG	161436
rs762473606	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625568	CACCACGCCCGGCTA[A/G]TTTTTGTATTTTTAG	161436
rs762494172	snp	G/T	1.66676e-05	0.00288679	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616780	GCCAAAGTCATCTCC[G/T]GTAACAAGACTGATT	161436
rs762496267	in-del	-/TC	5.43503e-05	0.00521269	intron-variant	EML5	GRCh38.p7	14:88627869	CCTGTTATAAATATT[-/TC]TGTTTCTAAAGCTTA	161436
rs762515831	snp	A/G	1.66103e-05	0.00288182	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740528	ACCCGTCTTACCAAA[A/G]ACACCTCGTTTTGGG	161436
rs762526660	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626374	TGCCTGTAAACCCAG[C/T]ACTTTGGGAGGTCAA	161436
rs762527363	snp	G/T	1.65745e-05	0.00287871	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658256	CTCGATAGCCTTCCA[G/T]CTCATTTGTCCACAC	161436
rs762561643	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88734180	ACAGAAAGGATTCTA[-/G]GGAACCACCTAACTT	161436
rs762581839	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88749771	GTATGTTCTCTGACA[A/G]AAACAGAATTAGAGT	161436
rs762592166	snp	A/G	0.000107588	0.00733364	intron-variant	EML5	GRCh38.p7	14:88621080	TTCTTTTTAGAAGTT[A/G]TAACCTCTTTTAAAA	161436
rs762616689	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671575	TTAAATGTAAATTGG[C/T]TAAATGCCCCAAATT	161436
rs762622692	snp	A/C/G	3.41911e-05	0.00413456	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665389	GTGATGAAAAGACAC[A/C/G]AGATCCTCTAGAGTA	161436
rs762625841	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701482	ACATTTCTTGGTACA[C/T]AGAATGTGCTTGATG	161436
rs762665676	snp	A/G	5.95291e-05	0.00545537	intron-variant	EML5	GRCh38.p7	14:88627840	TAAAGATAGTATCAA[A/G]AAGTTGTAATCTACC	161436
rs762669746	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88655202	AGAACAAAGCTGGAG[G/T]CATCATGCTAGCTGA	161436
rs762682613	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88667240	ATAATGTTTGTTATA[G/T]GTATATCTTTATTTG	161436
rs762685230	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88754202	CTAAGATATCATCCA[A/T]CTGTCCTGTCAAAAT	161436
rs762687165	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88769966	CAGCATTATGTGCAG[-/T]TTTTTTTTTTTTTTT	161436
rs762687650	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88716381	ATGCATAGACTCATA[C/T]AGCTGCCTCTGCATT	161436
rs762688951	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88739573	CTAAATATAAAACAA[G/T]AATATTAGAAAAATT	161436
rs762701465	snp	A/G	1.67851e-05	0.00289694	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696896	GTGGCCCTTTAATAT[A/G]GACAATGGTTTAATG	161436
rs762703991	in-del	-/T	8.29898e-05	0.00644112	intron-variant	EML5	GRCh38.p7	14:88661617	TTAACCATTTCATAA[-/T]TGATGATCATTAGGA	161436
rs762728462	snp	G/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613087	GCCAGCAGTCTACTG[G/T]TGTGTTGCCATTGCT	161436
rs762735412	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88649499	CATTTTATTAAACAT[A/G]CAAATACCATAGTTA	161436
rs762756522	snp	A/G	2.31677e-05	0.00340343	intron-variant	EML5	GRCh38.p7	14:88695484	TGAGAGAGATAAACT[A/G]ACTATTAACATTCAG	161436
rs762786278	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88670451	AGATAAACTCACAAA[G/T]ATGAGACAGAATCAA	161436
rs762801284	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88707817	GTCCTATGAGGTAAG[A/G]GCTCTTATATAGGAA	161436
rs762807403	snp	A/T	1.66638e-05	0.00288645	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712378	TTTATATCGTTGATA[A/T]CTGAATACTTGGGCC	161436
rs762814350	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88758602	TGATGTAGCCTCTTT[C/G]GAAAACCGCTTGGTA	161436
rs762833060	snp	A/C	1.9999e-05	0.00316214	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620770	TGATATCATGGATTG[A/C]ACATCTCCTGTCTCT	161436
rs762864196	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88793100	GACCGCGTCTCTGCA[A/G]GTGCGCGGGCCGGTG	161436
rs762872893	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617455	CTGACTGAAAACTGA[C/T]AGAACTATTTTTCAA	161436
rs762890325	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88790670	CAGACTAAATTATCT[G/T]GAGCAGGGCTTCAGT	161436
rs762902937	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88644757	ACTCTGTCGCCCATG[A/C]TGGAGTGCAGTGGTG	161436
rs762914717	in-del	-/CCGAAATCACACACTT			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615533	TTCCCAGCAGGTCTG[-/CCGAAATCACACACTT]CCCAATACAGGGGGA	161436
rs762919146	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692508	GTATTATCGGTAGTC[C/T]AGAAATGACTGAAAA	161436
rs762919555	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756494	TTATTAGATATTCTA[A/G]CCAAGAAAAATAGGC	161436
rs762932105	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88759965	CCTGATGACTACTCA[C/T]ATGGACTAATTGGTC	161436
rs762932220	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744592	TAACTCAAATTTTGG[A/G]GAGTCTCCAGGCTTC	161436
rs762935059	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88657369	TAATACTAAACTAAA[G/T]TATTACCTTTCATCA	161436
rs762940881	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778482	ATAGAACTGTGGAAG[A/G]TTAAGAAGTGGTAAG	161436
rs762977907	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88663842	ACCTGGCCAACATTT[A/C]TATATTCTATTTATG	161436
rs762990489	snp	A/G	1.81464e-05	0.00301212	intron-variant	EML5	GRCh38.p7	14:88627633	AAAAATCAAACACAC[A/G]AAAGAATCCTACCTT	161436
rs763029222	snp	C/T	2.10144e-05	0.00324141	intron-variant	EML5	GRCh38.p7	14:88618617	TAAAAGCAGAAGAAC[C/T]TGCCACCTGGGTATA	161436
rs763080654	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88750662	GAAAAGAAAGTTTTA[C/G]TATTTAAACTCCAAA	161436
rs763108659	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88645955	AGCTCTTCTCTAGAA[C/G]CTTTAATTTTTTTAA	161436
rs763112458	snp	C/T	1.65611e-05	0.00287755	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688363	TACACACATCTCCTG[C/T]GGATGTTCCAGAAAA	161436
rs763115997	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88736956	GCCATATTTGGGGAC[C/T]GCCCACCTTTGGGTG	161436
rs763120811	snp	A/G	1.91345e-05	0.00309304	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626788	GATGATCTAAGGCAA[A/G]AGAATGTAAAGTAGT	161436
rs763136857	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88632136	ATTTGGCTCACTGTT[C/G]AAGCAAAAAGTTCAA	161436
rs763146194	snp	C/T	1.67041e-05	0.00288994	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706293	AGCATCTTTCAGTTT[C/T]CTTTCAGGAATAAAT	161436
rs763190851	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88738867	GTAATAAGACATTTG[-/T]TTTGTTATTACCTTT	161436
rs763192905	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719367	CTCCAGCCTGGGCAA[C/T]AGAGCGAGACCTTGT	161436
rs763195355	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88683767	CATTTGATGAAAATG[C/T]TCCACAAATTTGGAA	161436
rs763199246	snp	A/G	5.15344e-05	0.00507588	intron-variant	EML5	GRCh38.p7	14:88705591	TCAGCCAGACTTTCT[A/G]TAATTTTTAAAAATG	161436
rs763203509	snp	A/C	2.82602e-05	0.00375889	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738944	AAAGTTAAATCCCAA[A/C]GACGAATACAACCAT	161436
rs763223433	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687026	TATTTTACCATGTGT[A/G]TCATAGAAAATAGAC	161436
rs763225851	snp	A/C	2.89918e-05	0.00380724	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726560	CTCTAAGTACAGTGA[A/C]TGAGCCATCCTTCAT	161436
rs763233552	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630683	TTTGCTTTGTGTCCT[C/T]ACGCAAAGTCAGGCT	161436
rs763248862	snp	G/T	1.80133e-05	0.00300105	intron-variant	EML5	GRCh38.p7	14:88621400	CTGCTTTCAGAGAAC[G/T]TTTTGCTTTGAGCTA	161436
rs763251828	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88657856	ATTTTTATGGCAAAA[C/T]ACATTTTCTATAACG	161436
rs763262923	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725587	GGCACTACATACCAC[A/G]TGAAGGATTATGAGC	161436
rs763276561	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713378	ACCTGGGCAACAGAG[C/T]GAAACTCCGTCTCAA	161436
rs763289913	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741900	TAAAAATTATGATCA[C/T]TATCTATTCAAAGAT	161436
rs763309742	snp	C/G	1.71823e-05	0.00293101	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642906	ACCTGTAGCAACATT[C/G]TGCAGAATTCCAACA	161436
rs763316552	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690063	CATGCTAGAAGAGTG[C/T]TCCAGGCAGAGGGAG	161436
rs763325164	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88762959	CGTTCTTTGAAACCA[A/G]TGAGAACAAAGACAC	161436
rs763363283	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88723714	TGTACGTCGTAAATA[C/T]ATACAGTTTTTATTT	161436
rs763367641	snp	A/C	3.05152e-05	0.00390598	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702609	GTATAAAACAGATTA[A/C]TTCGACAGTCATAAC	161436
rs763377951	snp	A/G	1.66369e-05	0.00288412	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88664553	TGCATATTCCTACTC[A/G]TTTACTACTCATTAC	161436
rs763380425	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88749415	AATCATCAGTAAACC[G/T]GCACTACAAGATATG	161436
rs763380721	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770335	TTTGTGTTCTATTTC[C/T]TATGCTTTTTCTAGA	161436
rs763388774	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712086	AAAGAATTTTCTAAT[A/G]AAACTTCATGACCAA	161436
rs763391214	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88775179	CAGGTAGGATACAGC[A/T]CATTATCAACTGTGG	161436
rs763402291	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88621006	ACCAGTTTCCCCTCA[A/G]AATGCTCAACAGAAT	161436
rs763411814	snp	A/C	1.6894e-05	0.00290633	intron-variant	EML5	GRCh38.p7	14:88746332	AAAAGGCAAACAAAT[A/C]AAAGAGAAACTGAAT	161436
rs763420878	snp	A/T	1.68658e-05	0.0029039	intron-variant	EML5	GRCh38.p7	14:88715211	CTGTTAAAAAGAAAA[A/T]AATGAGACTACATGA	161436
rs763423447	snp	C/T	1.85194e-05	0.00304292	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88663085	TTCAAAGAATAATTG[C/T]TCCTTAGCACCAGTG	161436
rs763427841	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676907	TCCTATTTATTTGTT[C/T]GTTTGTATTTTTTCT	161436
rs763433355	snp	A/G	2.79482e-05	0.00373809	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618747	GTGGGGCCCAGCGTT[A/G]GGTCATAAAAATCCA	161436
rs763436371	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88637047	ATGATTTTTAACAGA[A/T]GGAACAATAAACATT	161436
rs763457989	snp	C/T	1.6649e-05	0.00288518	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740535	TTACCAAAGACACCT[C/T]GTTTTGGGGTCAGAG	161436
rs763468643	snp	G/T	1.66222e-05	0.00288285	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746191	AATACTTACTCTATC[G/T]GTATGACCAGGAGCC	161436
rs763476282	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88729558	CATATACTTATTTGG[-/T]TTTTTTGTTTTTTGT	161436
rs763518357	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88776582	AGACAAAAGAAAAAA[G/T]AAAAAACAATGAAGT	161436
rs763534041	snp	A/C/T	3.34511e-05	0.00408958	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712307	GGAATAATTTTATAA[A/C/T]TCCATAGTCATCAGC	161436
rs763536427	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88625614	ACCTTGTTAGCCAGG[A/C]TGGTCTTGAACTCCT	161436
rs763542882	in-del	-/GAA			intron-variant	EML5	GRCh38.p7	14:88701592	GAAAGGAAGAAAAAG[-/GAA]GAAGAATGGGAGAAA	161436
rs763552884	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88630415	AGTCTCTGTAGTGAG[-/T]TAACTCCTTACTGCA	161436
rs763594985	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767088	CGAATATTAAGTTAT[A/G]AACTCTGAATCCTCT	161436
rs763608664	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88779281	CATAAAGAAAAAGCG[A/T]AACTATGAGTATCAT	161436
rs763610509	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88716427	CAAGTTAACATTAAA[G/T]CCATATACCGTATTG	161436
rs763628998	in-del	-/GT			intron-variant	EML5	GRCh38.p7	14:88734673	TACCATCAAGCAGGA[-/GT]GTACATCACCACCTA	161436
rs763657924	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88680305	CTAGTATTACAACCA[C/T]ATCTCAGGAGAAAAA	161436
rs763669919	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88752844	GAAGAGAAGTGTCTG[A/C]ATATCAAGAGGAGTT	161436
rs763674198	in-del	-/AGC			intron-variant	EML5	GRCh38.p7	14:88698743	CAAGTCCTTCTCTCG[-/AGC]AGCAGTTACTTTTCC	161436
rs763679117	snp	C/T	7.12669e-05	0.00596895	intron-variant	EML5	GRCh38.p7	14:88627640	AAACACACAAAAGAA[C/T]CCTACCTTCCTGCCA	161436
rs763691980	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88739336	AAACCCATAGATAGG[A/G]AGGGCTTTACATATG	161436
rs763695526	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88665928	AAAAAAAAATATTTG[C/G]TAAAAAGGTTGCCTC	161436
rs763734573	snp	C/G	1.65748e-05	0.00287874	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658257	TCGATAGCCTTCCAT[C/G]TCATTTGTCCACACC	161436
rs763742102	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687547	TTTACTTTTAGATAG[A/G]GCTTTAGAAACACAG	161436
rs763746595	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695805	TATTTAATTAAATTC[A/G]TCATAAGAAATTTAC	161436
rs763749850	snp	A/G	3.1452e-05	0.00396548	intron-variant	EML5	GRCh38.p7	14:88687210	CCCCACTAAGTCTCA[A/G]ATCACCTTTAGATCC	161436
rs763767024	snp	A/G	1.65633e-05	0.00287774	stop-gained, synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88626990	TATCTGAATCTGGTC[A/G]GAATTCTGCCACAAA	161436
rs763789687	snp	C/G	1.6625e-05	0.00288309	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658188	ATAAAATGACGTACC[C/G]CCATCTTCTTCAGAA	161436
rs763792430	in-del	-/CTG			intron-variant	EML5	GRCh38.p7	14:88713430	AATATTTTGATGATT[-/CTG]CTTTTATTCCATCCA	161436
rs763797474	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88620135	ATATTGAAGTTCTGA[C/G]GAAGGTTTCATTTGT	161436
rs763814948	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784993	TGGTATATATACACA[A/G]TGGAGTACTAGTCAG	161436
rs763823421	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88760179	TTTAATTTTTATGAA[G/T]TCTATCTAGTTCATT	161436
rs763841931	snp	A/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657434	TTCCTAACATTGGGC[A/G]AATATTTGTTGATAA	161436
rs763861669	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88649713	AACAATTTATCATAA[C/T]GAAGACCCTTATAAT	161436
rs763865371	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88716736	ACTGCTCACCAACAC[-/AC]ACACACACACACACA	161436
rs763874854	in-del	-/GTG	1.66341e-05	0.00288388	intron-variant	EML5	GRCh38.p7	14:88616917	AACTCATCATGGCAA[-/GTG]CGGGCAGGTTGACTA	161436
rs763901976	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617462	AAAACTGATAGAACT[A/G]TTTTTCAAATTAAAA	161436
rs763902983	snp	A/T	2.09989e-05	0.00324022	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620800	TCTTCTTTCCCCATA[A/T]TTTTAGAGAACTCAC	161436
rs763910996	snp	C/T	4.81128e-05	0.0049045	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726623	CAGCTGCACAACGAA[C/T]TGGTTCTTCCATATT	161436
rs763911045	snp	C/T	0.000114058	0.00755088	missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792317	GGTACCTGATGATGT[C/T]GTCGCTGTGGCCCCG	161436
rs763926124	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88639209	CTCATCATGGGAATA[C/T]GGTACTCCTGGACTG	161436
rs763926189	in-del	-/AAA	0.0194928	0.0967804	intron-variant	EML5	GRCh38.p7	14:88620935	ACATCTTCTGCATTT[-/AAA]AAAAAAAAAAAAAAG	161436
rs763944803	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88684695	GTCCTTTATTTTCTG[A/G]TAAGAAATTACTCAA	161436
rs763944911	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88655264	AAAACAGCATGGTAC[C/T]GGTACCAAAACAGAT	161436
rs763967374	snp	C/T	2.60332e-05	0.00360776	intron-variant	EML5	GRCh38.p7	14:88621084	TTTTAGAAGTTGTAA[C/T]CTCTTTTAAAAAAAT	161436
rs763981879	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88640706	AAAATAAATAACAAA[A/G]TCAGAGCAGAAATGA	161436
rs763993372	snp	C/T	2.39771e-05	0.00346236	intron-variant	EML5	GRCh38.p7	14:88695489	GAGATAAACTGACTA[C/T]TAACATTCAGAAGAG	161436
rs764015582	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88646028	AAATACTGAATAACC[A/G]GAACATTGAATTTAA	161436
rs764036630	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764774	GATATGTTGTATTTT[C/T]ACTTTCTTCTTCTTT	161436
rs764046780	snp	C/T	1.78004e-05	0.00298327	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88695402	CTTCCAGTCCCAGAG[C/T]ACAACAGTATGGCTA	161436
rs764061828	snp	A/G	4.97872e-05	0.0049891	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746233	TTTTCCCCTTTTCCA[A/G]TCCCAAACACAAACT	161436
rs764068026	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88670683	ATGATAAAACATTAC[A/G]GGAGCTGTTAACCAG	161436
rs764091169	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770093	AGAGCGCTTGTGAAA[C/T]GGCCGCTGAAATTTG	161436
rs764098015	snp	A/G	1.66178e-05	0.00288247	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746194	ACTTACTCTATCTGT[A/G]TGACCAGGAGCCATA	161436
rs764099336	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735861	AGGAGGTAGTTTTGT[A/G]CATTCTGATATGGAA	161436
rs764107198	snp	A/G	2.11267e-05	0.00325006	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88754656	TACCAACACTCGTTC[A/G]GGATGCAATGCAAGG	161436
rs764116756	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88782142	TGATATGGACAATAA[C/G]GTCCACCCTGAGGTG	161436
rs764120573	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88670808	TAGACCAAGCACAGG[A/G]AAGAATTTCAGAGCT	161436
rs764134823	snp	G/T	2.06665e-05	0.00321447	intron-variant	EML5	GRCh38.p7	14:88618625	GAAGAACTTGCCACC[G/T]GGGTATACAGTATTG	161436
rs764142945	snp	C/T	1.6947e-05	0.00291088	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88661804	ACCAAGTACACTTGT[C/T]CATGATGCCCAAGCA	161436
rs764168661	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88629813	CTGTTCTCAGTATCC[A/G]GGTTCCACTCTTGCT	161436
rs764174194	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783186	GAACCTCTGCTAGGG[A/G]AGTGCATAAAGGAAA	161436
rs764193008	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88729619	CAGGCTGTAGTGCTG[C/G]CGCAATCTTAGTTCA	161436
rs764231132	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719377	GGCAACAGAGCGAGA[C/T]CTTGTCTCAATCAAT	161436
rs764258354	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88683771	TGATGAAAATGCTCC[A/G]CAAATTTGGAATAAA	161436
rs764299191	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88658505	CAAGTGCAATGTGTT[-/A]AAAAAAAATGAGAAA	161436
rs764318873	snp	A/T	5.94195e-05	0.00545034	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657389	ACCTTTCATCAATTG[A/T]GGGTTCTTTTTGTTG	161436
rs764334117	snp	A/G	1.66145e-05	0.00288218	intron-variant	EML5	GRCh38.p7	14:88688512	AAGTACCACTTTCAA[A/G]ATGTACTCAATTATA	161436
rs764340423	snp	G/T	0.000134122	0.00818799	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618310	CTTCATAGACATGCC[G/T]TTTATAGCAGCCACT	161436
rs764340962	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88711317	GGGGCAGTTTCCCCC[A/C]TGCTGTTTTCGTGAC	161436
rs764353832	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720529	TAAAAACAAAGACCA[C/T]ATGATTATCTTAATA	161436
rs764368668	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88685628	CCATATATTTTTTTT[C/T]TCAGTAGGGTGGGGT	161436
rs764380858	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616002	TGCATAAATATGAGA[C/T]TCTGAAGAGCCATCT	161436
rs764389071	snp	C/T	1.65611e-05	0.00287755	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688385	TCCAGAAAAAGCCAT[C/T]TCTTCAGTCCATCCA	161436
rs764389099	snp	C/G	1.67307e-05	0.00289224	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706324	TTCCACTGAAAGACA[C/G]AGTGATCTGCTCCAC	161436
rs764389551	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88671622	CATGCTGATAAAGAG[A/T]CACAACCCACTGGTG	161436
rs764410502	snp	C/G/T	3.35145e-05	0.00409345	intron-variant	EML5	GRCh38.p7	14:88643035	GTCCTATAATGATAA[C/G/T]AATAAAACCATTATA	161436
rs764413285	snp	A/G	3.31994e-05	0.00407414	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616214	TTTGTCACATGGGGC[A/G]AATGACCCAAGAACC	161436
rs764417007	snp	C/G	3.3248e-05	0.00407712	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622638	CGAACACAATCTGTG[C/G]CTTGTCCTGTCTCAA	161436
rs764417842	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780253	TCACCACACCCAGCC[C/T]GTGTTTCTGAAAATT	161436
rs764420837	snp	C/T	4.57341e-05	0.00478173	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702628	GACAGTCATAACCTC[C/T]GTAACTAATATAGAA	161436
rs764422094	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758616	TGGAAAACCGCTTGG[C/T]AGCTATTCAAAAGGC	161436
rs764427508	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88675682	CTGCAGCTGGCTTGA[A/G]TTTCACCTCAGAAAA	161436
rs764442011	snp	C/G	6.63416e-05	0.00575903	intron-variant	EML5	GRCh38.p7	14:88705606	GTAATTTTTAAAAAT[C/G]AAATGTTACTTGTTT	161436
rs764461542	in-del	-/CTTT	0.000358719	0.0133877	intron-variant	EML5	GRCh38.p7	14:88694298	AGTAAAAAAGAAGCA[-/CTTT]CTTACCTGCTTTACG	161436
rs764482568	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88662028	AGAAAAATTTTAACA[C/T]AGTATTATTCAGAAT	161436
rs764494085	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725590	ACTACATACCACGTG[A/G]AGGATTATGAGCTGC	161436
rs764499517	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88637070	TAAACATTGTAAATG[A/C]TGTTTTGTGTTTTGT	161436
rs764505019	snp	G/T	1.82497e-05	0.00302068	intron-variant	EML5	GRCh38.p7	14:88621405	TTCAGAGAACTTTTT[G/T]CTTTGAGCTAATCTA	161436
rs764509520	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88775181	GGTAGGATACAGCAC[A/T]TTATCAACTGTGGTG	161436
rs764545609	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750699	AGAATGAATAATTTA[C/T]ATAAAAAGATACAGA	161436
rs764551909	snp	C/T	0.000306664	0.0123789	intron-variant	EML5	GRCh38.p7	14:88715219	AAGAAAAAAATGAGA[C/T]TACATGAACAGAAGT	161436
rs764559461	in-del	-/AAAGAA	1.67905e-05	0.00289741	intron-variant	EML5	GRCh38.p7	14:88684981	TAATCAATTGTATGT[-/AAAGAA]AAAAAAACAAATTAG	161436
rs764594364	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88622959	TTTTTTTCTGACATG[A/C]GCATAATTTTATTTA	161436
rs764611145	snp	C/T	2.25101e-05	0.00335478	intron-variant	EML5	GRCh38.p7	14:88754469	ATTTTCTATAATATA[C/T]CTTAACATACAATTT	161436
rs764618581	snp	C/T	5.0804e-05	0.00503978	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642915	AACATTGTGCAGAAT[C/T]CCAACAGATGCAGTG	161436
rs764626781	snp	C/T	3.35554e-05	0.00409592	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702484	TCAAAGGATGAATAG[C/T]TAGGCAGAGAATATC	161436
rs764645066	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88749423	GTAAACCTGCACTAC[A/G]AGATATGATCATGAA	161436
rs764656887	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88760479	ACCATATCTATATTA[-/C]CTTTTCCACAAATTG	161436
rs764684675	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88777013	AGACAGGAGTAGAAA[C/G]GTTATTCAAAGTGAT	161436
rs764686197	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88650717	GATCATAGCTCACTG[A/C]AGCCTCCAACTCCTG	161436
rs764687531	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764460	CAATAGTGATATCCT[A/G]ATGAATACTGGTAAT	161436
rs764693195	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794551	TTGTCACCAGGAGGG[C/T]GTTTTCTGTTTTTTA	161436
rs764701225	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88734788	ATGTTAAAATACACT[A/G]TGGGTATGCAATTAG	161436
rs764706521	in-del	-/C			upstream-variant-2KB	EML5	GRCh38.p7	14:88793316	TTGTGTGTCTTGCTG[-/C]CCTTATAGTGCTTTC	161436
rs764739672	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778365	GGTACACAAGAGTTA[A/G]AAACTTCAATTTTGA	161436
rs764758950	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88630450	CAGCATCCATTACAT[A/C]CTTTCTTCCTACCAA	161436
rs764766269	in-del	-/T	1.7328e-05	0.00294342	intron-variant	EML5	GRCh38.p7	14:88618216	TGCCTTGTGAATATA[-/T]TAAGTATTTACCTAG	161436
rs764784782	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88785273	GACCATTTGATGGCA[A/C]AACAGGGTGACTATA	161436
rs764815509	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764941	GCCTATTTTGGTAAA[C/T]GTTTTGGCACTTGAA	161436
rs764817332	snp	G/T	1.66034e-05	0.00288122	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616200	TGGTAAATCGAATAT[G/T]TGTCACATGGGGCGA	161436
rs764830117	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88653206	TTGGGCTGAGACAAT[-/AG]AGTTTTCTAAATATA	161436
rs764830445	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88677231	TTAATAAATGATGCT[A/G]GGAAAACTGGCTGGC	161436
rs764836589	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721054	AAATACCTAGGAATA[C/T]AGCTAATAAGAGAAG	161436
rs764840803	in-del	-/CTCA			intron-variant	EML5	GRCh38.p7	14:88780600	CTTTTAAGATGGAGT[-/CTCA]CTCACTGTGTCATCC	161436
rs764868182	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88624110	AAATGGGGTCTCACT[C/G]TGTCACCCAGGCTGG	161436
rs764868671	snp	C/T	3.18618e-05	0.00399123	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657433	ATTCCTAACATTGGG[C/T]GAATATTTGTTGATA	161436
rs764873172	in-del	-/A	1.91867e-05	0.00309725	intron-variant	EML5	GRCh38.p7	14:88627617	TATTCTTGTTTTTTT[-/A]AAAAATCAAACACAC	161436
rs764879887	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678616	GTTCCAAAATACTCA[C/T]AGTGATTAATACCAT	161436
rs764885194	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88640526	CAGAGACACAACATA[-/C]CAAAATCTTTGGCAT	161436
rs764892050	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88718873	TGTGAAAAAATAATG[C/G]ACGTACACAAAGAGT	161436
rs764905194	snp	G/T	3.57795e-05	0.00422947	intron-variant	EML5	GRCh38.p7	14:88621396	TGACCTGCTTTCAGA[G/T]AACTTTTTGCTTTGA	161436
rs764906034	snp	C/T	1.65721e-05	0.0028785	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685046	ATTGGGCCACTTTTA[C/T]CCACTTCTAGTATTT	161436
rs764945165	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717048	TTCATAATACATCAC[A/G]AAGTAAAGGTACAGA	161436
rs765017810	snp	A/G	1.65627e-05	0.00287769	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88626959	ACATGTTTTACTCCC[A/G]CTGAGACAAACTGGG	161436
rs765025747	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665577	CATGCCTATAATCCA[A/G]GCACTCTGGGGAGCT	161436
rs765036161	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706091	TCACACTCTGTGACA[C/T]CTAACTTTAAACATA	161436
rs765043643	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88635209	GATTGTTTTTTGCTT[C/T]GGTAAAGCTTTATAT	161436
rs765050868	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88677352	AACTATAAAAACCCT[-/A]GAAGAAAATCTAGGC	161436
rs765067872	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630664	GTATCTTCTCAGTTC[A/G]CAGTTTGCTTTGTGT	161436
rs765068036	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653548	TTCTGCATCTATTGA[A/G]ATAATCATGTGGTTT	161436
rs765071470	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88708690	ATTGAAATCAAAAGA[C/T]TAGTGCTTGAGCATC	161436
rs765076474	snp	A/G	4.27141e-05	0.00462117	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618804	AGATACCGGGAATCC[A/G]GACTAAATCTGAATC	161436
rs765076696	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88742677	TCAAACACACTGTCC[A/C]TCAAAGATGAACAAG	161436
rs765077347	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88670529	CCAAATTAACACAAC[A/G]CCTCTCCAGCAAGGG	161436
rs765110034	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88667736	CACTGGCATGAAGGG[A/G]GCCTGATGGCATTCA	161436
rs765131444	snp	C/T	5.05029e-05	0.00502483	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712291	CTTAAACATGGATAT[C/T]GGAATAATTTTATAA	161436
rs765133841	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788491	ATATTTCAGATGCAT[C/T]GTCATTTGAGCTCAT	161436
rs765138902	snp	A/C	1.88081e-05	0.00306655	intron-variant	EML5	GRCh38.p7	14:88627624	TGTTTTTTTAAAAAT[A/C]AAACACACAAAAGAA	161436
rs765144330	in-del	-/ATC			intron-variant	EML5	GRCh38.p7	14:88688987	AATTTTTCTATAAAT[-/ATC]ATCCTGTATGTATTC	161436
rs765164284	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88787810	TCTAATACTTTTTGA[A/G]GCACTACTTCTACAT	161436
rs765178617	snp	A/G	1.67902e-05	0.00289738	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740412	CCTTGTATTGTTCGT[A/G]TAAGATTGATTCCTT	161436
rs765188925	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88637263	AGAATGGAGCTACAT[A/G]TATAATCTAAAATTT	161436
rs765192675	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88654874	AATATTGACAGTGGG[G/T]TGTTAAAGTCTCCCA	161436
rs765194201	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615937	TTTCAGTTGTGCTTT[C/T]AGGTTACATGTGTAA	161436
rs765201505	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88699876	GATTAATCCTATTTA[-/T]TCTCCATTTTAGATA	161436
rs765263200	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744523	GAACTGTTTACATAA[A/G]GAATCCAAACACTGA	161436
rs765272142	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88691204	ACACTAGGATCTATG[A/T]GTCACTGGGGTAGTG	161436
rs765289398	snp	A/C	9.99217e-05	0.00706759	intron-variant	EML5	GRCh38.p7	14:88688234	CTACACTCCAGGACA[A/C]ATTTTGTTTAATTTA	161436
rs765291452	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780836	CCTTGTCCTCCCAAA[A/G]TGCTGGGATTACAAG	161436
rs765292228	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88643061	TTATATTCTTCCTCA[C/T]GTATAAATGTTCACC	161436
rs765312008	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88711349	GTGAGTGAGTTCTCA[A/C/T]GAGATCTGATGGTTT	161436
rs765331031	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88617110	TTAATCTTTTTAAGA[-/T]TAAAGTAGTACTTTA	161436
rs765334335	snp	A/G	1.70223e-05	0.00291734	intron-variant	EML5	GRCh38.p7	14:88646907	GAAGATGACAAAAAT[A/G]CAAAGTTAGGCTTTG	161436
rs765338367	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88682195	CTTTGGGAAACACAA[C/T]AAAATACCTCTGTAA	161436
rs765350555	snp	A/G	3.31664e-05	0.00407211	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705490	AAATTACCTGTCGAC[A/G]GTAGGTGAGCTGTGT	161436
rs765374557	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88686928	CACAAGTTCCTGACT[C/G]GTGATAAATGTGATG	161436
rs765387159	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88734568	AGAAAAAAAATGTAA[C/G]AAAGTGACAATGAAA	161436
rs765395799	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88669072	ACCTGGGAGCTGCAC[A/G]GGACAAGGGGAGCTC	161436
rs765412109	snp	A/G	1.67175e-05	0.0028911	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705584	ATGAGAGTCAGCCAG[A/G]CTTTCTGTAATTTTT	161436
rs765416195	in-del	AAATACAGGGTTCCCCTTTTTCCCC/TTAATACAGGGT			intron-variant	EML5	GRCh38.p7	14:88662559	TTTTTTTTTTTTTTT[lengthTooLong]CTCACTTTGTCACCC	161436
rs765426894	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88684465	GTGAGCCACCGCGCC[C/T]GGCCTGTTTTATTAT	161436
rs765454193	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88634290	TTCCTGAGGCCTCCC[A/C]AGCCCCATTTCCTGT	161436
rs765454635	snp	C/T	1.66724e-05	0.0028872	intron-variant	EML5	GRCh38.p7	14:88665517	GAGCATATTAGGCAA[C/T]TTTCCCTTTTTTCTA	161436
rs765466942	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88782052	AGACTTGGAGGGCTC[C/T]GAAGACAGGAAGATG	161436
rs765491266	snp	C/T	1.7216e-05	0.00293389	intron-variant	EML5	GRCh38.p7	14:88624943	TCACAAATGCATAAA[C/T]ATTCTGTGAAAAGAA	161436
rs765499030	snp	A/G	1.65649e-05	0.00287788	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621290	ATTCCTTGTCCCAAC[A/G]AGGATCTTGCCCTGA	161436
rs765508086	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735646	AAATTTAAAATGCAC[A/G]CATCCTTTGACTACT	161436
rs765508500	snp	A/G	3.31752e-05	0.00407265	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644472	TACATTGTTTGTCTG[A/G]AGTTTCTCTGGCTGT	161436
rs765524004	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768559	GGAATTACAGGTGCC[C/T]GCCTCCACACCTGGC	161436
rs765574969	snp	G/T	3.3123e-05	0.00406945	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736470	TAATTAGAAAAGGTT[G/T]ATTTCTTTCTTGCAC	161436
rs765577440	snp	A/C	3.31505e-05	0.00407113	intron-variant	EML5	GRCh38.p7	14:88688480	ATCCTCCCCCTAGTT[A/C]ACAAAAAATATTATG	161436
rs765585789	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88700934	CACTGTGAGTTACTC[-/A]ATAGTTCTTTAAATA	161436
rs765628866	snp	A/T	9.67118e-05	0.00695317	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638897	ATGTTCCTGATAAAA[A/T]CTCTGAGAACCTACA	161436
rs765629907	in-del	-/TAGTAAAT	2.69502e-05	0.00367074	intron-variant	EML5	GRCh38.p7	14:88695498	GACTATTAACATTCA[-/TAGTAAAT]GAAGAGAGAAAACAT	161436
rs765630974	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674319	AGACTTGGTAATTTA[C/T]AAAGGAAAGAGATTT	161436
rs765635022	in-del	-/AATT	7.53835e-05	0.0061389	intron-variant	EML5	GRCh38.p7	14:88715243	CAGAAGTCACAACAG[-/AATT]AATGCCGTTTCAAAC	161436
rs765645912	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88774074	AGAGAGCCGAGTTCA[C/T]GCCACTGCACTCCAG	161436
rs765654645	snp	A/G	1.66297e-05	0.0028835	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88746188	GAGAATACTTACTCT[A/G]TCTGTATGACCAGGA	161436
rs765691232	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88635708	ACCACAAAGAACCAT[G/T]GAAGCTCATGTGTGG	161436
rs765696280	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88724949	CAACAGGGAGGTTTC[A/G]TAGTCTTTCATCTCT	161436
rs765707361	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88723370	AAAGACAGATACTGC[A/G]TGATCTTGCTTATAT	161436
rs765716329	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762881	AACCATACAACTACA[C/T]GGAAACTGAACAACC	161436
rs765744509	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88620625	AGCCATATTTTAGCA[C/T]ACAATTTATAATACG	161436
rs765775073	snp	C/T	4.96824e-05	0.00498385	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688348	AGATGTCTCTCCAGA[C/T]ACACACATCTCCTGT	161436
rs765799882	in-del	-/T	1.95505e-05	0.00312648	intron-variant	EML5	GRCh38.p7	14:88621104	TTTAAAAAAATTATC[-/T]GTACTTACTTTATCA	161436
rs765819858	snp	C/T	5.01945e-05	0.00500946	splice-donor-variant	EML5	GRCh38.p7	14:88744022	AAGACCCTTCTAGTA[C/T]CTTGATATGTTTTAC	161436
rs765831515	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88775062	ACTCCTGGCAGCATT[C/T]ACCACCTGCTAACTG	161436
rs765834735	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88675763	TGCTCTGGTTCCCTT[A/T]AAAAACTGAATACTT	161436
rs765852360	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653225	TTTTCTAAATATAAA[A/G]TCATGTCATCTGCAA	161436
rs765879481	snp	C/T	1.67885e-05	0.00289724	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621126	ACTTTATCAGCAATA[C/T]CCCAAAGTCTCACTG	161436
rs765944820	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88776822	GGAGTCAGAGGTTGC[A/C]GTGAGCTGAGATTAT	161436
rs765947085	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88742328	ATGTACTGCTAGTGT[C/G]ACTGAGGAAATGAAT	161436
rs765954003	snp	A/G	2.49604e-05	0.00353264	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615892	CAGGGAGTTAATTAT[A/G]TTTTTAGATTTTCAT	161436
rs765958659	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88677019	AAGCAATTCTCTTGC[C/G]TAAGCCTCCCAAGTA	161436
rs765960566	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88725947	AGCGAAGGATCTTAC[C/T]GTTCACTGAGGTAGA	161436
rs765961205	in-del	-/TAAT	0.000102685	0.00716464	intron-variant	EML5	GRCh38.p7	14:88634503	ACCTATAATGGAAAA[-/TAAT]TATCTATAAATAACA	161436
rs765962976	snp	G/T	9.05346e-05	0.00672749	intron-variant	EML5	GRCh38.p7	14:88627938	AAACAAAAACTGTAC[G/T]TAACAAAGAACAGCT	161436
rs765964246	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88690142	TAACATCCAGGGAGA[C/G]AAGTATGGAGCAGCA	161436
rs765975657	snp	G/T	1.65556e-05	0.00287707	intron-variant	EML5	GRCh38.p7	14:88681856	TAGAAAACTGTGAGA[G/T]CTTAATCTACGTTCA	161436
rs766004244	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88740756	AAGCTACGTTATAGC[A/G]TAGCTATATAGTCAC	161436
rs766012031	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88675953	TGCTCCAGTTCCCAA[A/C]AAGTTCCTCATCTCC	161436
rs766015243	snp	C/T	4.37972e-05	0.00467939	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88638874	GTGAGGCACAGAATA[C/T]CATCATTATGTTCCT	161436
rs766025085	snp	C/G/T	3.48088e-05	0.00417174	synonymous-codon, missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696946	GAATTGAGGGATCTC[C/G/T]ACCAACCTAAAATAG	161436
rs766035883	snp	A/G	1.67517e-05	0.00289406	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661760	TCTGTAACTTCTCCA[A/G]TTACTGGCCAAATTC	161436
rs766046600	snp	C/T	1.71143e-05	0.00292521	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702460	CCTGGCCTGTTGCCA[C/T]GTAGTCTTTCAAAGG	161436
rs766087624	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88691055	AGAGTCTGGGCTGGT[A/C]CCCACCTACAAGCTA	161436
rs766091132	snp	G/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712449	AGCCCAATGAACACC[G/T]TTTATTTCTTCTGTA	161436
rs766095832	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88622842	GATATTTATAATTTA[A/C]CTCTAATATTCTTGT	161436
rs766100152	snp	C/T	1.66496e-05	0.00288522	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715036	GATGAAACTAAGGGA[C/T]CCCAAACACTCGCCA	161436
rs766110462	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88734346	GTAAGTATTAGAATG[C/T]CACCATTTGAAATTC	161436
rs766139901	snp	C/T	1.70892e-05	0.00292306	stop-gained, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706353	ACCAATAGAAATAAC[C/T]CACTGATAATCATGT	161436
rs766146536	snp	A/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681955	CATATTCTTAAGGTT[A/T]TATCATCGCTTACAG	161436
rs766153193	snp	C/T	1.66776e-05	0.00288765	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88714947	TTGTTACCTGGCATT[C/T]TATAAAAAAGTCTTT	161436
rs766163896	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717512	GCCTGTAATCCCAGC[A/G]GTTTGGGAGGCTGAG	161436
rs766173124	snp	C/G	2.02595e-05	0.00318266	intron-variant	EML5	GRCh38.p7	14:88618633	TGCCACCTGGGTATA[C/G]AGTATTGGTACTGTA	161436
rs766179678	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692363	GCCTGGGCAACAGAG[C/T]GAGACTCTGTTTCAA	161436
rs766180019	snp	A/G	4.03527e-05	0.00449163	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88657417	TTGTAAATGAGGCTT[A/G]ATTCCTAACATTGGG	161436
rs766184639	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88764763	TTACAAATTTTGATA[C/T]GTTGTATTTTCACTT	161436
rs766186027	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88661833	CAATTTTTTCTACCT[-/A]AAAATGAAAAACAAT	161436
rs766194649	snp	C/T	1.84269e-05	0.00303531	intron-variant	EML5	GRCh38.p7	14:88705630	CTTGTTTAAAGAAGA[C/T]TCATTTTCAAAACAG	161436
rs766199869	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88668737	ATAAAGCAGGTAGAA[A/G]GTTGAGTTTAAGGGA	161436
rs766212897	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88755898	CAGCTACTTGAGGGG[A/C]TGAGGTGAGAAGATC	161436
rs766226817	snp	C/T	1.83149e-05	0.00302607	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626812	AAGTAGTCAAAGTCA[C/T]ACTATGTGCATTTTA	161436
rs766229562	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780724	GGGATTACAGGCGCG[C/T]GCCATCATGCCCAGC	161436
rs766231463	snp	C/G	5.14134e-05	0.00506992	intron-variant	EML5	GRCh38.p7	14:88682039	ATGTGTCCCTATAAA[C/G]AAAACATAGGATCAA	161436
rs766238480	snp	A/G	1.7029e-05	0.00291791	intron-variant	EML5	GRCh38.p7	14:88658140	GCTTAAACAAGTTGT[A/G]CTAAATTTTCCCTAT	161436
rs766241207	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690219	CAGTACTGCAGGCCA[C/T]TGTAAGGACGGCCTA	161436
rs766249726	snp	A/G	1.72059e-05	0.00293303	intron-variant	EML5	GRCh38.p7	14:88738862	GCCTAGTAATAAGAC[A/G]TTTGTTTTGTTATTA	161436
rs766262918	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14	GRCh38.p7	14:88613627	TTGTTGGATGACGTG[A/G]TTTAAAATGATCACC	161436
rs766265917	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741055	GTAATCCCAGTTACT[C/T]GGGAGGCTGAGGCAC	161436
rs766313180	snp	A/G	1.66189e-05	0.00288256	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88704919	TCTTCTTTTAGAAGT[A/G]GCACTTTTTTGTTTC	161436
rs766315901	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785026	ATAAAAAAACGAGAT[C/T]CTGTCATTTGCAACA	161436
rs766319047	snp	A/C/G			intron-variant	EML5	GRCh38.p7	14:88774005	GTGCCTGTAGTCCCA[A/C/G]CTACTTGAGAGGCTG	161436
rs766336289	snp	A/T	2.39759e-05	0.00346228	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88739003	ACAAGCATTCATGCT[A/T]AAAATTCCTGCCTAG	161436
rs766358436	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88703660	GTCAGGTAAGAAAAC[A/G]AATGCTGGGTGAATG	161436
rs766368352	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674244	ACTGCACTTCAGGCT[A/G]GGCTAAAAGGGTGAG	161436
rs766372647	snp	C/T	1.6609e-05	0.0028817	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616185	CATGTCGATCACCAC[C/T]GGTAAATCGAATATT	161436
rs766382862	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88676404	ATGCCAGACACATGA[-/T]AACCATCAGAAGTCA	161436
rs766389640	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88756539	AAAAGTAAAAGTAAA[G/T]ATCTCTATTGGCAGA	161436
rs766415570	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88769768	AAATCATGAATTCGT[A/G]TCAACACTTCAGATT	161436
rs766422147	snp	A/G	1.65622e-05	0.00287764	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736415	GGTTTAGTAGGATGG[A/G]CAGCAAGTGCCCAAA	161436
rs766453402	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88746855	GAAGCGGAGGCAACT[A/C]ATGAAGAGGGAGAAA	161436
rs766464406	snp	G/T	1.76686e-05	0.0029722	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665379	TATCTTTTCTGTGAT[G/T]AAAAGACACAAGATC	161436
rs766481541	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88636994	GTAACTGGCTAAAAT[A/C]GTACAAAATCAAACA	161436
rs766482460	in-del	-/TGGTT	1.67877e-05	0.00289716	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88696901	CTTTAATATGGACAA[-/TGGTT]TGGTTTAATGGTCTC	161436
rs766490105	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704713	CCTCATGATTAGATT[C/T]AGGTGATGTGTTTTC	161436
rs766503769	snp	A/G	8.01828e-05	0.00633127	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726609	TCCATCTGCATTGAC[A/G]GCTGCACAACGAATT	161436
rs766523853	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761892	ATCACCATTCTAACT[C/T]GTATGAGATGATATC	161436
rs766535924	in-del	-/CTT	2.29724e-05	0.00338905	cds-indel, nc-transcript-variant	EML5	GRCh38.p7	14:88738981	CACCAGTAGCAAAGC[-/CTT]CTTCACAAGCATTCA	161436
rs766574694	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88747651	TATGAGCAAAGAATA[C/G]GAGACTATAAAAAGT	161436
rs766583894	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711136	TGTGCATGGTGACTC[C/T]CATGTCCTGGCTATG	161436
rs766589267	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88647591	CAGCTACATGGGAGG[A/G]TGATGTGGGAGAATC	161436
rs766591197	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88680914	GTCAGCAGAAAAAAA[A/T]CAAAAACCAAAACAA	161436
rs766614018	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783453	TATAAATACACACAC[A/G]GACTGAAAATAAAAG	161436
rs766617284	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660023	ACTCGCGCCTGTAAT[C/T]CCACCACTTTAGGAT	161436
rs766667742	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733059	AAGTCATTTGAACAA[C/T]TAATGCTATTTGAAT	161436
rs766668998	snp	C/T	3.32834e-05	0.00407929	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618282	TGATCCATAAGATGT[C/T]TTCCTGAAGGCACTT	161436
rs766678283	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88779898	ACTACAAAATTTTTA[A/C]TTCTATGTTACTGTG	161436
rs766687740	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88655002	AGTTAGGTCTTCTTG[C/T]TGCATTGATCCCTTT	161436
rs766707651	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88701320	ACAAATAATTACCTG[A/C]CCCGAAACATCAATA	161436
rs766717452	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88730647	ACAGATACTACTCAA[C/T]TGTTTATTTGGGGAG	161436
rs766735775	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642498	TTCCAGCCCCAGCAA[C/T]CACTCACCCAACATG	161436
rs766747077	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88750810	GAGTATTTACTATTT[C/G]GGAACCAAAGGGCAT	161436
rs766749309	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88724635	AGGTGTTTTACATGC[A/G]TCTTAAATTCTTGTA	161436
rs766756140	snp	C/T	2.05227e-05	0.00320327	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754651	GTTGCTACCAACACT[C/T]GTTCAGGATGCAATG	161436
rs766769038	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88753817	AAAAATATAATTTTA[A/T]TAGACAACCTTTAAG	161436
rs766797298	snp	A/C	0.000218324	0.0104458	intron-variant	EML5	GRCh38.p7	14:88658415	GAAAATTCAAACAAT[A/C]TTTCTGAGAAATTTC	161436
rs766818086	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88750304	CTTCACAGGGGTCAC[G/T]ATGAGAATCAACATA	161436
rs766822962	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784931	CAATAGCTAAGATTC[A/G]GAAGCAACCTAAGAG	161436
rs766840379	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617802	TTTTTCATTGGCCAA[A/G]AAAATGGATAGTCAT	161436
rs766852738	snp	C/T	6.08032e-05	0.00551343	intron-variant	EML5	GRCh38.p7	14:88687369	ATAAAGATCTAAATA[C/T]TTTTTAAAATAGTAA	161436
rs766870255	snp	G/T	2.55281e-05	0.00357259	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687226	ATCACCTTTAGATCC[G/T]GGGGCCAATGCAGCT	161436
rs766881733	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88737449	AGTATAAGCCAAGCG[C/T]AGCCTGCCAGGCCAA	161436
rs766903616	snp	A/G	2.37088e-05	0.00344294	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687234	TAGATCCTGGGGCCA[A/G]TGCAGCTCTTTTTAT	161436
rs766925248	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673019	TGAAAAAAAGGGACT[C/T]CTCCCTAACTCATTT	161436
rs766938871	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88739137	AAGAATAAACAAATA[C/T]ATCAGAAAACACAAA	161436
rs766967062	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613280	CCTCTTCATTCTAAA[A/G]GTTTACTCCATTGAA	161436
rs766970173	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88651059	ATATTCTAAGTTGGT[-/AA]AAGAGATATGAACCT	161436
rs766971302	in-del	-/AAC			intron-variant	EML5	GRCh38.p7	14:88655121	TTCCTCACAGAATTG[-/AAC]TACTGTAAATTTCAT	161436
rs766993325	snp	C/G	1.72424e-05	0.00293614	intron-variant	EML5	GRCh38.p7	14:88714915	ATAGGTACTACAAAT[C/G]TATAATTTGCTAGAA	161436
rs766999142	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766812	TCCCCCAGACACCCA[A/G]CTTTAAAATTTCTCT	161436
rs767025627	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88704582	TATATTACACACAAT[C/G]TAATGTATTACTCTA	161436
rs767035677	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88703538	TGCACTTCAAAGAAA[A/C]CCAATTCATAAAATA	161436
rs767040771	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88739773	TTCAAATGAATAAAG[C/G]AAAGAAAACCAATTC	161436
rs767044621	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88755794	GGTCAGGAGTTCAAG[A/T]TCACCCTGGGAAACA	161436
rs767045775	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88668714	TATTCTGCTGGTTGG[C/G]TGCAGGCATAAAGCA	161436
rs767048148	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88787434	TCCACGTTTTCCTTA[A/T]TGTATATCCAAAACA	161436
rs767059825	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721838	AAGAGGCAACCTACA[A/G]AGTGGGAAAAAATAT	161436
rs767099718	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88740816	GGGTTTGAATCAGAT[G/T]ATTTTTAAAATATGC	161436
rs767108699	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641276	GAAGCCAGCATCACC[C/T]TCATACAAAAACCTG	161436
rs767115270	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88786464	GTGTTCAGTAAATAT[A/T]TGCTGAAAGAACAAG	161436
rs767127626	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698069	AAGATATAACAAATA[A/G]CACTGCAATCAGCCA	161436
rs767129137	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88649827	AGTTAAATGTTTTAT[A/G]GGGAAAAAATACCTT	161436
rs767135253	in-del	-/CAC	1.67393e-05	0.00289299	cds-indel, nc-transcript-variant	EML5	GRCh38.p7	14:88682010	TGTAGCTAAACCCCA[-/CAC]CACCTCTCCTTCCAT	161436
rs767138199	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88723784	AAATTTTTAAAAAGG[C/T]AGACTGGTTACAAAA	161436
rs767145949	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88688724	CCCTTAGCACTTTTG[A/T]TGATGTTTTTTAAAG	161436
rs767153969	snp	A/G	9.99867e-05	0.00706989	intron-variant	EML5	GRCh38.p7	14:88658397	ATTTCCCCTAAAGAG[A/G]AAGAAAATTCAAACA	161436
rs767166237	snp	A/C	8.34397e-05	0.00645855	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712392	ATCTGAATACTTGGG[A/C]CAAATTCCATTTACT	161436
rs767179997	snp	A/C	2.79014e-05	0.00373496	intron-variant	EML5	GRCh38.p7	14:88627894	AAGCTTATGCATATT[A/C]ATCTGTGAAACATGG	161436
rs767205153	snp	A/G/T	5.48896e-05	0.00523855	intron-variant	EML5	GRCh38.p7	14:88687343	CTATGGAAAAAAAAA[A/G/T]GTTCAAGTTAATAAA	161436
rs767217007	snp	A/T	1.70391e-05	0.00291878	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627674	CCAAATGGTAATAGT[A/T]TGTTCTGGGTCTAGT	161436
rs767222606	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88742113	TGCCTGGACTCCCAA[C/T]TGAGATGAACTGAGA	161436
rs767234222	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88779464	AAGGGATAATGGCAC[A/G]TCTTTCATTTACATC	161436
rs767236492	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88747582	ATAACATAAGCTTAA[C/T]GTGAGAAATAAGCTT	161436
rs767277455	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88642319	ATGCTAACAGAACAT[G/T]ATTTGCTCTTGAATA	161436
rs767281791	in-del	-/GAA			intron-variant	EML5	GRCh38.p7	14:88619677	ACAACTTGAATCTTG[-/GAA]GAAGAATTTTTTTTT	161436
rs767286924	snp	C/G	3.47578e-05	0.00416866	intron-variant	EML5	GRCh38.p7	14:88736614	GCTGTAATAATGATA[C/G]CAGCAGGAGGCAGAC	161436
rs767302761	snp	A/T	1.67975e-05	0.00289802	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740552	TTTTGGGGTCAGAGC[A/T]TTTCCACATAAACTC	161436
rs767314299	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88665922	CAAAAAAAAAAAAAA[-/T]ATTTGCTAAAAAGGT	161436
rs767325864	snp	A/C	3.31719e-05	0.00407245	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625067	CCACGATTCTACACA[A/C]TATGTGATCTTTCCA	161436
rs767328593	snp	A/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626699	CTAGATTTTTGAAAG[A/T]TGAAATATATGCTTG	161436
rs767336981	snp	A/C	1.70009e-05	0.0029155	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88646954	AGGATTACCTGGAAC[A/C]TCTTTTCAGCAGCAG	161436
rs767350484	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612511	ACAAAATTATACAAA[-/T]TTTTTTTACAAGTAT	161436
rs767354957	snp	A/G	6.62482e-05	0.00575497	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736520	CTGTCCTGTGTTCCA[A/G]CTAGAATGTGGTCAC	161436
rs767355682	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88624008	TTGTGTTTAATTAAC[-/AT]ATGTGGGTTCTTTCA	161436
rs767358408	snp	C/T	0.000114305	0.00755907	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615874	AATCAGAGAAGAAAA[C/T]TGCAGGGAGTTAATT	161436
rs767359146	snp	C/T	1.68672e-05	0.00290402	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696926	GGTCTCTGTATCCCA[C/T]ATATGAATTGAGGGA	161436
rs767369183	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88667724	ACAGAGCCCGGGCAC[G/T]GGCATGAAGGGGGCC	161436
rs767382426	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88793552	CAAATGTTTTGCTTT[A/G]TTTTTAAGTTTATTT	161436
rs767390454	snp	A/G	0.000101032	0.00710675	intron-variant	EML5	GRCh38.p7	14:88665537	CCTTTTTTCTAATTT[A/G]AAGTATGGGCCAGGT	161436
rs767398534	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88680745	AGTAAACACGGGTTA[C/T]ATTGTTTTTCAAAAA	161436
rs767407337	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88625729	CCTGGCCTGGTCTTA[C/T]ATTAAGAATACCCAA	161436
rs767408004	snp	A/C	0.000108301	0.00735792	missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792376	CTGTACACCACGCCG[A/C]CCCCCGCCACGAAGT	161436
rs767417559	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88782122	TTTGTCTAAAATGAT[G/T]ATAGTGATATGGACA	161436
rs767439587	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88729748	GTATTTTTAGTAGAG[A/G]CAGGGTTTTGCCATG	161436
rs767443324	snp	A/G	1.66701e-05	0.002887	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665410	CTCTAGAGTATCCGC[A/G]TTTGCCATTAAGAAG	161436
rs767444393	in-del	-/A	2.16424e-05	0.00328949	splice-donor-variant, frameshift-variant	EML5	GRCh38.p7	14:88616723	ACAAAACACAAACTT[-/A]ACAAATTTTTCTGGA	161436
rs767455650	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88681705	ATGATGATAGGAGGT[C/G]CCATAAAGCCAAGAC	161436
rs767481634	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88687063	AAAGATGGCAATGAT[C/T]CTGGTATCCAGTTAA	161436
rs767491067	snp	C/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715076	TAACGCTGAGCAACT[C/G]CATAAATATCAACCG	161436
rs767493068	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88732911	TGCCTCCCAGGTTCT[A/G]GCGATATTATTAAAC	161436
rs767521439	snp	A/G	3.3123e-05	0.00406945	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621221	CCCATCCACATGACC[A/G]TTAACTAAAATATTA	161436
rs767524944	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88632340	TTTCTCTCTTCCCCC[G/T]CTACATTCTCAATAA	161436
rs767527009	snp	C/T	1.65858e-05	0.00287969	intron-variant	EML5	GRCh38.p7	14:88726494	ATTACTTATATTCTG[C/T]ATCACTGAAGATAAA	161436
rs767539406	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88771576	CTGCTCCTCATTCAA[A/G]GCAAAACTTCTCAAA	161436
rs767542270	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768271	TACAAAGTTTTTCTT[C/T]GTAGTCACTAAGTAT	161436
rs767559121	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617716	AAGTGATCCTCCCAC[C/T]TCGGCCTGCTACATC	161436
rs767563568	snp	C/T	1.66316e-05	0.00288367	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642946	TGATAAATTATATCA[C/T]CACCATCATTTAAAT	161436
rs767572487	in-del	-/CAC			cds-indel, nc-transcript-variant	EML5	GRCh38.p7	14:88736483	TTTATTTCTTTCTTG[-/CAC]CACAATTTCAAAAAT	161436
rs767577249	snp	A/G	1.87454e-05	0.00306143	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754627	TAAGGCTCTTTCCCA[A/G]CTTGTCCTGTTGCTA	161436
rs767577367	snp	A/C	1.66518e-05	0.00288542	intron-variant, utr-variant-3-prime, missense	EML5	GRCh38.p7	14:88616114	TAGTAACATAGTCTG[A/C]TCTTCATGGGCTGAG	161436
rs767580041	snp	A/C			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661692	TCACAAATCCCAAAT[A/C]GTCCCCGGTAGCTAG	161436
rs767617555	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88716532	GGCACTATTTGGCAG[C/G]TTTTACTTTTTATGC	161436
rs767623639	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644533	CAGAGAAGTGGGGAG[A/G]AGGAAAGGCATGCAG	161436
rs767626170	in-del	-/T	1.66477e-05	0.00288506	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88740426	TATAAGATTGATTCC[-/T]TTCCAAACATATATA	161436
rs767628975	snp	A/G	3.52547e-05	0.00419835	intron-variant	EML5	GRCh38.p7	14:88754498	TTAGAAAAAAATGAA[A/G]AACTGTCACATACCT	161436
rs767664057	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88708163	TAAGAGAAACCAGTA[A/T]TTTTAGTCAATGGGA	161436
rs767671286	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88664817	CAAAATAATTTTTTA[C/G]TGTAACAAATTAGTT	161436
rs767686411	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88690998	ACTTCTCTGCACCCA[-/G]GGTCTGCCTCCCTGG	161436
rs767691243	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671750	AAGCAGGGAGTGCAA[C/T]CCTAGTTTCTAACAA	161436
rs767706534	in-del	-/TTG			intron-variant	EML5	GRCh38.p7	14:88727041	CCTGGCTATGTTTTG[-/TTG]TTGTTGTTGTTGTTG	161436
rs767739146	in-del	-/TTG			intron-variant	EML5	GRCh38.p7	14:88714474	GATCTAATATACAGC[-/TTG]TTGAGTACAGTTAAT	161436
rs767744148	in-del	-/TTTT/TTTTTTC			intron-variant	EML5	GRCh38.p7	14:88729863	CCACACTCGGTCTTG[-/TTTT/TTTTTTC]TTTTTTGTTTTTTTT	161436
rs767753236	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619049	CATCTCCCAATTCCT[C/T]TAAAAACGTCTAATG	161436
rs767765206	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88760282	TTTTATAGTTTGTCT[C/T]ACATTTAAAGCTACA	161436
rs767765566	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88664188	AGGCTGAGTTGGGAG[A/G]ATGACTTAAGCCCAG	161436
rs767776802	snp	C/G	1.66172e-05	0.00288242	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664590	TATATCTATAAAGCT[C/G]TCATGGGATGCTACA	161436
rs767790637	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692755	TACAAATGTAAAAAT[A/G]CTTCTTTTTACTTTG	161436
rs767795560	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88759205	CATTACTGTCTGTAC[A/C]CATATTTTTAGTATA	161436
rs767820547	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88746813	AGCAGTAAACCTCTC[A/G]GAAACAACAAATAAC	161436
rs767826278	snp	C/T	4.42742e-05	0.0047048	intron-variant	EML5	GRCh38.p7	14:88695358	ATCAAGTTTTTTTCC[C/T]ACCTTGCTATTGAAA	161436
rs767826335	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88791046	AACCAACTGAATACA[A/G]AGCACCACCTCATTC	161436
rs767832803	snp	A/G	0.000112164	0.00748796	intron-variant	EML5	GRCh38.p7	14:88663154	AATATTTACACATAT[A/G]AAATACATACAAATA	161436
rs767836169	snp	G/T	1.66363e-05	0.00288407	intron-variant	EML5	GRCh38.p7	14:88616913	AGAAAACTCATCATG[G/T]CAAGTGCGGGCAGGT	161436
rs767843751	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88707750	GGAATAAATTTTTTA[C/T]GTAGCTTAATATAAG	161436
rs767848767	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88713282	CTGTAATCTCAGCTA[C/T]TCGGGAGGCTGAGGT	161436
rs767922410	snp	C/T	1.65778e-05	0.002879	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88616807	GATTCCTGAATGAGA[C/T]ACACAGGCACAGTTG	161436
rs767929001	snp	C/T	1.66029e-05	0.00288117	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740436	ATTCCTTTCCAAACA[C/T]ATATATCCCCATTGA	161436
rs767985375	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88783339	GACTAAAATCTCCAA[C/T]CAAAAGAAATAGAGT	161436
rs767991147	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88660524	GAAGTGGGCGGATCA[C/G]AAGGTCAGGAGTTTG	161436
rs767998617	snp	C/T	1.66059e-05	0.00288144	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622657	GTCCTGTCTCAAGCC[C/T]GAAGGCACGGCACCG	161436
rs768001045	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88677907	AAAGACCTAGAACCA[C/G]AAACACCATTTGACC	161436
rs768017140	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88700090	CCCACAACATTTAAT[A/G]CTTTTGAATAGGAAG	161436
rs768024821	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750802	CCTCCTGAGAGTATT[C/T]ACTATTTGGGAACCA	161436
rs768034038	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88696218	CTATGGATAATTTAT[C/T]ACTTCAGTCAGAGCA	161436
rs768034537	snp	C/T	3.69501e-05	0.0042981	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726599	CAAGATGGATTCCAT[C/T]TGCATTGACAGCTGC	161436
rs768046664	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88630765	AAGGATTTTTTTGCT[G/T]CTTTCCCACTGGATA	161436
rs768058462	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88780544	CTAAAATCCACAGGG[A/C]AGGGCAGCAGTTGAT	161436
rs768065998	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88638427	GGAAGCAGGGTTCTA[-/C]CCCGCCCAGTCTAGT	161436
rs768070128	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88685782	ACTTTTAGATTGCTT[A/G]TATCTAGTAGAATGT	161436
rs768072673	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88652456	GAATATAAAATCCAT[-/A]AGGTGCAAACTCAAA	161436
rs768082072	in-del	-/TTC	1.68809e-05	0.0029052	intron-variant	EML5	GRCh38.p7	14:88643051	AATAAAACCATTATA[-/TTC]TTCCTCATGTATAAA	161436
rs768084764	snp	A/G	5.04147e-05	0.00502044	intron-variant	EML5	GRCh38.p7	14:88643042	AATGATAATAATAAA[A/G]CCATTATATTCTTCC	161436
rs768089055	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88681565	TAGTCCCCACTATGC[C/G]TTAGAAAAGTTTCCA	161436
rs768089407	snp	A/G	0.000508609	0.0159388	intron-variant	EML5	GRCh38.p7	14:88687334	TACAAACCCCTATGG[A/G]AAAAAAAAGGTTCAA	161436
rs768099898	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641501	TCATCATTCCTGGCA[C/T]GCAAGGTTGGTTCAA	161436
rs768125433	in-del	-/ATGACCAG			intron-variant	EML5	GRCh38.p7	14:88720171	AACCAAAAAAGGCTC[-/ATGACCAG]ATGAATTTATAGCTG	161436
rs768130177	snp	G/T	5.01618e-05	0.00500783	intron-variant	EML5	GRCh38.p7	14:88644527	CTGCAACAGAGAAGT[G/T]GGGAGGAGGAAAGGC	161436
rs768144487	snp	A/G	0.000190849	0.00976668	intron-variant	EML5	GRCh38.p7	14:88705020	ATTCTTAGAATATAT[A/G]CTAATAAAGGTGTTC	161436
rs768165179	snp	A/G	4.98384e-05	0.00499167	intron-variant	EML5	GRCh38.p7	14:88616897	AGAGGGAAGGAACAA[A/G]AGAAAACTCATCATG	161436
rs768180380	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88737385	ACAGCACACCCGGCC[C/T]AGCCACAGGCTGAGC	161436
rs768207242	in-del	-/TAA			intron-variant	EML5	GRCh38.p7	14:88726403	ACATCTGAAATATAT[-/TAA]TAAGAAGGGGAAGAG	161436
rs768253436	snp	A/C	1.6922e-05	0.00290873	intron-variant	EML5	GRCh38.p7	14:88622737	AGTAAATAACCAAGC[A/C]AGAGTAAGTGTTCAT	161436
rs768254881	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88685490	TCAATTCAAGATATA[C/T]AGTCAGCCCTCAGTA	161436
rs768255320	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780759	TTTGTATTTTTGGTA[A/G]AGACGGGGTTTCATC	161436
rs768258197	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755860	TTTAATGAGCCAGAC[A/G]TAGCAGCATACACCT	161436
rs768259738	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748356	TAACCAGAATGAAGA[C/T]ACCTCTTTGAACTCG	161436
rs768279814	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88627996	AAAAGGAGTTTTGGG[G/T]GTGGGGAGGAAAGAA	161436
rs768280708	snp	C/T	0.000200568	0.0100122	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705545	TTCTGGAACATCAGA[C/T]AGATCTGAATCTGAT	161436
rs768288036	snp	G/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767988	TAGCAACTTCCAGTC[G/T]CTATAAAACTTTCTT	161436
rs768301601	snp	A/G	3.31241e-05	0.00406952	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621215	GATTGGCCCATCCAC[A/G]TGACCGTTAACTAAA	161436
rs768330636	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672643	ATTAATAAAATAGAT[C/T]ATTAGCTAGACAAGA	161436
rs768342867	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88618552	GGAGGAGTTGAGAAG[C/T]TGGAGCTCTGGAGCT	161436
rs768358354	snp	C/G	1.66399e-05	0.00288438	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88704884	AAGTGTAATCGAATA[C/G]TATTTCCTGGAGCCC	161436
rs768359369	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88654668	TATGATTTCTGTTCT[G/T]TTGCATTTGCTGAGG	161436
rs768373235	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768689	AGTGCTGGGATTACA[A/G]GCGTGAGACATCGCA	161436
rs768400185	snp	C/G	1.66054e-05	0.00288139	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715004	TATCTACTGTCTGAA[C/G]ACCAGTCCAGATGAG	161436
rs768406418	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721567	CTGGCCAGCTATATG[C/T]GGAAAACTGAAACTG	161436
rs768412954	in-del	-/GGGC			intron-variant	EML5	GRCh38.p7	14:88691285	GCAGACAGAATGTCT[-/GGGC]AATGGCAACTGGGTG	161436
rs768425009	in-del	-/AATTA			intron-variant	EML5	GRCh38.p7	14:88741930	TCTAATGAGTACTTT[-/AATTA]AACTTTGTAATTTTT	161436
rs768430849	snp	C/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88792925	AGCCTGGCGGACCCG[C/G]GCCGCGCACCCCGAA	161436
rs768457274	snp	C/T	0.000172176	0.00927677	intron-variant	EML5	GRCh38.p7	14:88744130	TTAAAATACTTATTT[C/T]CAGAATCATTTAAAA	161436
rs768506023	snp	C/T	1.67953e-05	0.00289782	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696913	ACAATGGTTTAATGG[C/T]CTCTGTATCCCATAT	161436
rs768539909	in-del	-/AGCT	1.67002e-05	0.00288961	intron-variant	EML5	GRCh38.p7	14:88627090	TTATTACAAGAACCA[-/AGCT]AATCAACAGCATCAA	161436
rs768544064	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88722780	CATAAAAAAAAATTT[A/G]CAACCCCTGGCATAA	161436
rs768551683	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88675013	TCCCATGGTCTTGGG[A/C]AGCTCTGCCCCTGTG	161436
rs768563805	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88688089	ACAAAACACTGCAGA[C/T]CTATTTCATTCTGTG	161436
rs768570178	snp	A/C	1.85235e-05	0.00304326	intron-variant	EML5	GRCh38.p7	14:88638954	AAATTTTAAGATGTA[A/C]CAGCCAAAAGCACTT	161436
rs768577228	in-del	-/GTG			intron-variant	EML5	GRCh38.p7	14:88619304	CAGGAGGCACAGGTT[-/GTG]GTGAGCTGAGATTGC	161436
rs768588224	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88691852	AAAGCCTTAACATTC[A/C]TCCTTTTATGCTTCA	161436
rs768592916	in-del	-/G	2.49794e-05	0.00353399	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88657459	TGATAAGGCTCTGAT[-/G]GTGTAACTGATTTCA	161436
rs768600619	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88702382	AAAGAGATATGTGAT[G/T]AATTTATTTAAACTC	161436
rs768608582	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88759108	TGACTATACTAAAAA[C/T]CACTGAATTGTGCAC	161436
rs768613912	snp	C/G/T	3.4619e-05	0.00416035	intron-variant	EML5	GRCh38.p7	14:88714910	ATTGTATAGGTACTA[C/G/T]AAATCTATAATTTGC	161436
rs768625261	snp	A/T	7.42308e-05	0.00609179	intron-variant	EML5	GRCh38.p7	14:88638796	TGTTTCTTTTTAAAA[A/T]ACAGAAACATACCTA	161436
rs768643751	snp	C/T	1.71876e-05	0.00293147	intron-variant	EML5	GRCh38.p7	14:88627844	GATAGTATCAAAAAG[C/T]TGTAATCTACCTGTT	161436
rs768652369	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88665274	AATAAAAATTATACA[A/T]TGATACATTTATACA	161436
rs768654727	snp	A/G	1.65619e-05	0.00287762	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688283	TACTTTTTCCAATGC[A/G]TGCATACTGAACACT	161436
rs768655145	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88693667	TACTTTTAAAAAATA[A/C]ACTAATTTTAGATAA	161436
rs768655759	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88700381	CCTCTGCAACAATTA[C/T]TTGTTTTTTTTTCTT	161436
rs768667137	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88659401	GTTTTTAATAGAGAC[A/G]GGGTTTCACCATGTT	161436
rs768678220	snp	C/G	1.69663e-05	0.00291253	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661707	CGTCCCCGGTAGCTA[C/G]AACCATTTTGTCACT	161436
rs768772183	in-del	-/AAAT	6.38413e-05	0.00564948	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615848	TACACATTTCCAGAC[-/AAAT]AAGCTGCAATCAGAG	161436
rs768773222	snp	C/T	1.65831e-05	0.00287945	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658233	TTCACTATCACAAGG[C/T]CTTTTTTCTCGATAG	161436
rs768779140	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88666790	GGATTTTGGTATCTT[G/T]TATGAAATCTGATGA	161436
rs768780448	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88747304	GTAATTCCATCTACT[C/T]GGGAGGCTGAGGCAG	161436
rs768795803	snp	A/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614663	TCTTCAGGAAACTAC[A/G]GATAGGCTAGACAGC	161436
rs768812736	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88772653	AGCTACTGGGGAGGC[A/T]GAGGCAGAAGAATCG	161436
rs768813392	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625141	TTCTGAAAAGGAGTG[A/G]GGGAGGGGGAGACAA	161436
rs768816994	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88738768	GGTGAAGAGGCAAAT[A/G]TAAGTCTTATTTATA	161436
rs768826238	snp	A/G	3.33778e-05	0.00408507	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685139	TTATCTTCCAAGAGA[A/G]GACCTGAAATGTTAA	161436
rs768832037	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88648765	ATGTAGAGATCAGTA[C/T]TGAGTAAGCTATTCT	161436
rs768835036	snp	A/G	1.65677e-05	0.00287812	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626911	AGCCCTTTTTTGCTA[A/G]GAAGAGCTCTTCCTG	161436
rs768855350	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88716281	ATAAATCCAAGATTG[C/T]ATTATTTGAAGCTTC	161436
rs768855391	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88737136	ACTTGGAACTCACCA[A/C]ACAGTGAGTACAGAC	161436
rs768865036	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784480	ATACTGCAGAAATTC[A/G]AAGGATCATTAGTGG	161436
rs768880740	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766632	CAGTCCTGTGATCTC[A/G]CCCTGCCTCCATTTG	161436
rs768896765	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88736025	TTTTTTTTTTGAGAT[G/T]GAGTCTCACTCTGTT	161436
rs768899372	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88784060	ATGACCAGTGGGTCC[A/G]TGAAGAAATTAAAAA	161436
rs768920021	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88785682	AGTAAATCATGCTAC[C/T]TCTATCTTCAAAATA	161436
rs768923600	snp	A/G	3.87702e-05	0.00440268	intron-variant	EML5	GRCh38.p7	14:88712221	TTCTGCAAGAACACG[A/G]AAGTCTTCTGTGAGA	161436
rs768938196	in-del	-/GAGT			intron-variant	EML5	GRCh38.p7	14:88644416	TTCAGTAACACTGGA[-/GAGT]GAGTTTTCCTTACCT	161436
rs768980492	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727128	TGTTTTGCCATCTAA[C/T]TGAATAACAGTAAAG	161436
rs768987959	in-del	-/CTTCC			intron-variant	EML5	GRCh38.p7	14:88637173	TTCTTATTCTTTAGT[-/CTTCC]CTTGAGTCTATCTTA	161436
rs769000988	snp	A/T	3.32524e-05	0.00407739	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664573	CTACTCATTACATTG[A/T]ATATATCTATAAAGC	161436
rs769002622	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654468	TGTCCCAGAGATTCT[A/G]GTATGCTGTATTCTT	161436
rs769009465	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88686913	AATATCAAAGTTGCA[C/T]ACAAGTTCCTGACTG	161436
rs769016691	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88788243	TCCAATTACAATTTT[C/G]ACTTGCGTTGAATAA	161436
rs769047520	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690810	TCCTTGAGTAGATGA[A/G]AGAAAGAATCTAGTG	161436
rs769067732	snp	C/T	5.5622e-05	0.00527332	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620889	CTGTAACACACAGTA[C/T]GAGCAGCATGTCCCA	161436
rs769069158	snp	C/T	2.95871e-05	0.00384613	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726565	AGTACAGTGAATGAG[C/T]CATCCTTCATTCCAA	161436
rs769069286	snp	C/G	0.000128908	0.00802727	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792261	GCGGGTGCAAACTCC[C/G]GGAGCGGCTTGCAGG	161436
rs769072148	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666060	TTCTGAATACAACAA[A/G]AGCAAGTATGGATAT	161436
rs769079818	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717556	AAGATCAGAGAGAGA[C/T]CATCCTGGCTAACAC	161436
rs769084380	in-del	-/AAA			intron-variant	EML5	GRCh38.p7	14:88670867	ACTACAAGATTAGAG[-/AAA]AAAAAAAAGGATGAA	161436
rs769087551	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88745586	TTATTTTTCACCTTA[A/G]CCATAATACATATGT	161436
rs769090055	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733138	CAAGAAGTGAGGTCT[C/T]CACTGCCACACAAAT	161436
rs769101221	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88664256	CATTCCAGCCTGGGT[A/G]ACAGAGTGAGACCTG	161436
rs769104612	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88676914	TATTTGTTTGTTTGT[A/G]TTTTTTCTGAGACAG	161436
rs769108509	snp	C/T	1.67981e-05	0.00289806	intron-variant	EML5	GRCh38.p7	14:88664674	TCTTTGGAAATACTT[C/T]TTTACACTCTGCAAC	161436
rs769122248	snp	C/T	3.62155e-05	0.00425516	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754610	AATCCCAAATACAAA[C/T]ATAAGGCTCTTTCCC	161436
rs769140326	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88706990	TTCCAACAATGTCCT[G/T]TATAATCATTTTAAA	161436
rs769143419	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88761468	TGGTTTTCTGTTCCT[A/G]TGTTAGTTTGCTGAG	161436
rs769150658	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88776597	TAAAAAACAATGAAG[C/T]GGGTCGGGCATGGTG	161436
rs769180685	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88709742	AACCTGCATTTAATA[A/T]CAAAAGATGGGAAAT	161436
rs769203272	snp	C/T	1.68069e-05	0.00289882	missense, downstream-variant-500B, nc-transcript-variant	EML5	GRCh38.p7	14:88622606	TGGAACATCTTACTT[C/T]GCCTCTGCACACAGA	161436
rs769208820	in-del	-/A	1.73773e-05	0.0029476	intron-variant	EML5	GRCh38.p7	14:88714899	ACTCTAAAATATTGT[-/A]ATAGGTACTACAAAT	161436
rs769212425	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88728638	AGGAGGAAGAGAAGA[A/G]GCTTGTCTTACGATC	161436
rs769213257	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88745992	ATCAAATCATGTTTC[C/T]AAGTCCTACAATACA	161436
rs769213951	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638528	TTAAACCTTTTTGCT[A/G]ACCAGAAATTCCTGC	161436
rs769231628	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88693445	CAGATCTCATGAGAC[A/G]TATTCACTTCCACAA	161436
rs769242580	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88785206	GGTCGTGGAGGACTC[-/AG]GGGGAAGTGGGGATG	161436
rs769260692	snp	A/G	1.6782e-05	0.00289668	intron-variant	EML5	GRCh38.p7	14:88664670	TCTATCTTTGGAAAT[A/G]CTTTTTTACACTCTG	161436
rs769260846	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88639823	TGGCCTCAAGTGATC[C/T]GCCCATCTTAGCCTC	161436
rs769261943	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88693911	AAGAAGCTGGGACCA[C/G]AGGTACACACCACCA	161436
rs769293386	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88774761	TTTATCTAAACTCAC[C/T]CCTTCAGTGGTCTCA	161436
rs769297534	in-del	-/TACA			intron-variant	EML5	GRCh38.p7	14:88777650	TTAAGACATACGCAG[-/TACA]TACAATAAGATAGAA	161436
rs769297883	snp	C/T	0.000107145	0.00731853	intron-variant	EML5	GRCh38.p7	14:88695323	AGTCCAAAGTAATTC[C/T]AGTATTTTGCAAATG	161436
rs769306538	snp	C/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792127	GAGTCCCTAGACGAG[C/G]AAGAGGGGAAAGGCA	161436
rs769312604	snp	A/T	1.69092e-05	0.00290763	intron-variant	EML5	GRCh38.p7	14:88644412	ACATTTCAGTAACAC[A/T]GGAGAGTGAGTTTTC	161436
rs769313367	snp	C/T	8.6367e-05	0.00657085	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726554	ACCTTACTCTAAGTA[C/T]AGTGAATGAGCCATC	161436
rs769351263	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659189	ATGAGAGATGTCTTA[C/T]ACAAAACACAGTGAT	161436
rs769359787	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88640177	AACTAACAAAGAAAT[C/T]CTGGACTTGAATTCA	161436
rs769393667	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88618479	ACAAAAACTTAATAG[A/G]AGAAAAGCTCTGATA	161436
rs769419698	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647286	GGAGAACTGCTTGAA[C/T]CCAGGAAACGGAGGT	161436
rs769426693	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752374	GTAGGTTTGTTTTAT[A/G]ACATTTTATGCTATG	161436
rs769429034	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779061	GCAAGCAACCATCAA[C/T]GTTCAAGGTAATCAC	161436
rs769431233	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794630	GAGAAAAAGAAAAAT[C/T]GTTGATTATTTAAAT	161436
rs769469138	snp	C/G	3.91888e-05	0.00442638	splice-acceptor-variant, intron-variant	EML5	GRCh38.p7	14:88627820	TAGAAGGAGCTGTAG[C/G]TAAATAAAGATAGTA	161436
rs769475199	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88685476	TTAGTAATTTTAATT[C/G]AATTCAAGATATATA	161436
rs769477236	snp	C/T	5.18345e-05	0.00509064	intron-variant	EML5	GRCh38.p7	14:88618217	TGCCTTGTGAATATA[C/T]AAGTATTTACCTAGT	161436
rs769481666	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88749735	AAAGTGTCAATAAAT[G/T]TTAAAAAATTAAAAT	161436
rs769491754	snp	A/G	3.33762e-05	0.00408497	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88704868	TTTATACCCGTGAAC[A/G]AAGTGTAATCGAATA	161436
rs769511389	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88695920	ACTACTTTTAGTAAA[A/G]GTCAATCATTCAAGC	161436
rs769524377	snp	C/G	1.6574e-05	0.00287867	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88658341	CCAGCGAACATTTGT[C/G]ACATGTGTACTATGG	161436
rs769585775	in-del	-/T	4.57091e-05	0.00478042	intron-variant	EML5	GRCh38.p7	14:88687176	AATGAGCAATTAATC[-/T]TTTTTTCCTATACAA	161436
rs769599425	in-del	-/ATATATACACACACAC			intron-variant	EML5	GRCh38.p7	14:88699951	TAGTGAATTATATCT[-/ATATATACACACACAC]ATATATACACACACA	161436
rs769608854	in-del	-/TA	2.01266e-05	0.00317221	intron-variant	EML5	GRCh38.p7	14:88618636	CACCTGGGTATACAG[-/TA]TTGGTACTGTACCTG	161436
rs769619971	snp	G/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793085	TTGCGGAGTCGCTGG[G/T]ACCGCGTCTCTGCAA	161436
rs769633873	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88784240	ATACATCTTAAAGAA[A/C]TAGAAAAGCAAGAGC	161436
rs769638543	snp	C/T	1.75962e-05	0.00296611	intron-variant	EML5	GRCh38.p7	14:88740599	ATAGTATAATCAAAT[C/T]ACCAAAGAATTCTTA	161436
rs769638757	snp	A/G	1.66585e-05	0.00288599	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712374	TGAATTTATATCGTT[A/G]ATATCTGAATACTTG	161436
rs769671402	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88789949	TGACTTTTTATTACT[A/G]AAGCTAAGGTTACAG	161436
rs769679396	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88720158	TAAATAGCCTACCAA[A/C]CAAAAAAGGCTCATG	161436
rs769684954	in-del	-/ATCT	1.67705e-05	0.00289568	intron-variant	EML5	GRCh38.p7	14:88658413	AAGAAAATTCAAACA[-/ATCT]TTCTGAGAAATTTCA	161436
rs769713401	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88770956	AAATTAATTAGATAT[A/C]AGCACTGTCATCAAA	161436
rs769729155	snp	A/C/T	3.31511e-05	0.0040712	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658252	TTTTCTCGATAGCCT[A/C/T]CCATCTCATTTGTCC	161436
rs769786989	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88741238	AGTCATCATAGACTA[A/C]GAAGAAGAAAAAGGA	161436
rs769802878	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672584	GAGACACGAAAAGCG[C/T]GTCAAAAAATATTAA	161436
rs769810314	snp	A/G	2.03975e-05	0.00319349	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687316	ACCATCTTTTCCTCC[A/G]GTTACAAACCCCTAT	161436
rs769822897	snp	C/T	6.63196e-05	0.00575807	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616854	CATGTCTGGACCAGA[C/T]TCCCAAAACCTCATC	161436
rs769825053	in-del	-/ATAG			intron-variant	EML5	GRCh38.p7	14:88763242	TGAAAAGATAACAAA[-/ATAG]ATAGACAGCTAGCAA	161436
rs769833010	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88633580	ATAGTGCTCAAAGTC[G/T]GTGAATTATAATTGT	161436
rs769854175	snp	C/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765485	TTCTTCTCAAGCTTT[C/G]AATCTTTCTGACTTC	161436
rs769858623	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676540	GAGTGGGGACACAGC[C/T]AAACTATATCACTGC	161436
rs769869056	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643877	AATCACCATCGCACA[A/G]CTTTACGCCTTGTTT	161436
rs769882302	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88726816	GGCAAGAAATTCTTA[C/T]CTATGAAAATGGGAA	161436
rs769890469	snp	G/T	3.43808e-05	0.00414599	intron-variant	EML5	GRCh38.p7	14:88625170	AAACTCATCAAAAGT[G/T]CAAATAGAGTTTAAA	161436
rs769896364	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88759881	CTCTCACCAGCAATG[A/T]AAGAAAGTTCCAGTT	161436
rs769907810	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677747	AAAACCACATTGAGA[C/T]ACCATCTCACACCAG	161436
rs769925325	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88623671	CCCACCTCGGCCTCC[C/G]AAAGTGTTGGGATTA	161436
rs769951971	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88764320	CAATTGTGTGGAATT[C/G]GAATCATTTATTCTT	161436
rs769960454	snp	C/T	1.65806e-05	0.00287924	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681962	TTAAGGTTTTATCAT[C/T]GCTTACAGTAGCACA	161436
rs769961995	snp	C/T	8.14432e-05	0.00638083	intron-variant	EML5	GRCh38.p7	14:88657359	TTTCTTCATCTAATA[C/T]TAAACTAAATTATTA	161436
rs769964292	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663598	CATACTCATTAAGTT[C/T]TTTATGTTATATGAT	161436
rs769975197	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752001	TAATGCAGGCTTAGC[A/G]TAATACCTGGCACTT	161436
rs769992616	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88739228	TCACTGGCTCACTTA[C/T]ATGGATTTTTTCAAT	161436
rs769996894	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88750566	TACTATTAGTTTACC[A/T]TAACCTTAATTAGCT	161436
rs770007064	snp	A/G	1.66893e-05	0.00288867	intron-variant	EML5	GRCh38.p7	14:88621344	GAATGTAATACAACA[A/G]CTGCTTTTCTTCTTC	161436
rs770017538	snp	C/T	0.000167425	0.00914791	intron-variant	EML5	GRCh38.p7	14:88702421	GTGTAGCTTATCTGG[C/T]TTATTGTCAGTCTTT	161436
rs770044614	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721708	AGGTCATGGGCATGC[A/G]CAAAGATTTCATGAA	161436
rs770052615	in-del	-/T	1.66618e-05	0.00288628	intron-variant, utr-variant-3-prime, frameshift-variant	EML5	GRCh38.p7	14:88616093	GTTGTATTAAGTCTC[-/T]TTAACTAGTAACATA	161436
rs770053464	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761084	TTATTTGGAATTTTC[C/T]ATGTAGGCAATCATG	161436
rs770103861	in-del	-/TA	2.38371e-05	0.00345224	intron-variant	EML5	GRCh38.p7	14:88620734	ATATACTAGAAACTC[-/TA]TTCCATTTGTTCACT	161436
rs770113515	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88712059	TGCATTCATAACAAC[-/AT]ATGAATTCAAAAAGA	161436
rs770113695	snp	C/T	1.70304e-05	0.00291803	intron-variant	EML5	GRCh38.p7	14:88736606	TATATAATGCTGTAA[C/T]AATGATAGCAGCAGG	161436
rs770128917	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741760	GGGCAGAGATACATA[C/T]ATTAAATAGTTCTGC	161436
rs770141865	snp	A/G	1.67136e-05	0.00289076	intron-variant	EML5	GRCh38.p7	14:88746312	AAGAAGTCCAGGAAG[A/G]AATAAAAAGGCAAAC	161436
rs770143005	in-del	-/TGTG			intron-variant	EML5	GRCh38.p7	14:88729141	TTTTCCTTTCCAATC[-/TGTG]TGTGTGTACGTGTAC	161436
rs770155723	snp	C/T	1.65701e-05	0.00287833	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626895	TTCCAGTGTGCTCAG[C/T]AGCCCTTTTTTGCTA	161436
rs770159357	snp	A/C			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615154	ACTGATGGCTCGAAA[A/C]TGAAAATGGAAATGT	161436
rs770201767	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88784142	ACCTATGGGATACTG[-/C]AAAAGCAATACTCAA	161436
rs770204710	snp	A/G	1.68955e-05	0.00290645	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706276	TGGGGTGCTATGTGA[A/G]CAGCATCTTTCAGTT	161436
rs770216039	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88650949	ACCTGGCCTGTTTTC[C/T]ATATAAAGTGCTTTA	161436
rs770216948	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88781471	ACAATACCAATGATA[C/G]TACCACTAATTATAA	161436
rs770226682	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88669962	GGGACCCAGGCAAAG[-/AA]GGTCTGGAGTGGACC	161436
rs770261849	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725451	TTAGTTAAAGAGTAC[A/G]AAGTTTCAGTTAGAA	161436
rs770275455	snp	A/C	2.52944e-05	0.0035562	intron-variant	EML5	GRCh38.p7	14:88620711	TACAAATGGAAGTTA[A/C]ATCAAGTATATACTA	161436
rs770289863	snp	A/G	2.5621e-05	0.00357908	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618736	TTCTGTTAAGAGTGG[A/G]GCCCAGCGTTAGGTC	161436
rs770293615	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88787247	TACATACCATATCAC[A/G]GGTACATTAGTGCTA	161436
rs770297340	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88783844	GAATATTTCATCCAA[A/T]GGCTACAGAATGCAC	161436
rs770317233	snp	C/T	1.75872e-05	0.00296535	intron-variant	EML5	GRCh38.p7	14:88621384	AAATGACCCTATTGA[C/T]CTGCTTTCAGAGAAC	161436
rs770317348	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88719867	GGTTTTTTGAAAAAA[A/T]TAATAAAATAAATAG	161436
rs770327612	in-del	-/TTCT			intron-variant	EML5	GRCh38.p7	14:88761219	TTAAAATTATTATTA[-/TTCT]TTAAGTTCTGAGATA	161436
rs770330844	snp	A/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614344	AAGCTTCTTAGCCCC[A/G]TAATCAGTCCTTCAG	161436
rs770358282	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88617101	GTTTCTAGATTAATC[G/T]TTTTAAGATTAAAGT	161436
rs770375247	snp	C/T	2.84248e-05	0.00376983	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706419	AATATATTTTCTAAA[C/T]TTGGCCCCTATAATA	161436
rs770396772	snp	C/T	1.788e-05	0.00298993	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642894	TCAGGGTTTCCTACC[C/T]GTAGCAACATTGTGC	161436
rs770409145	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654576	TTGTTCAGTTTCCAT[A/G]TAGTTGTATGGTTCA	161436
rs770422491	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88788181	CTGAACCCATATAAA[C/G]ACAAAAAAAATCTAT	161436
rs770430728	snp	C/T	2.00975e-05	0.00316991	intron-variant	EML5	GRCh38.p7	14:88740372	AAAGTGTTTAAAATA[C/T]TTAAATGTACTTACA	161436
rs770431990	snp	A/C/G			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615680	ACAGATCAGTCTTTC[A/C/G]CTATTTTGATGATTC	161436
rs770447892	in-del	-/T	6.91061e-05	0.00587778	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88661820	ATGATGCCCAAGCAA[-/T]TTTTTTCTACCTAAA	161436
rs770456172	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638686	ATTGGGTAGGGCTTT[A/G]TGTATACATAGATTT	161436
rs770456311	snp	A/C/G	3.33947e-05	0.00408613	intron-variant	EML5	GRCh38.p7	14:88746307	TGTCCAAGAAGTCCA[A/C/G]GAAGGAATAAAAAGG	161436
rs770475711	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88776057	ACAATTACAGCATTA[C/T]TGGGCTTGGGGTGCC	161436
rs770479863	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88689071	TAGAAAACTCACTTT[C/T]ATAACCACATAGCAT	161436
rs770486405	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672349	GTCCTTTGAAACCAA[C/T]AAGAACATGGAGACA	161436
rs770513076	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88732634	GGGATGGCATTGAAT[C/G]TATAAATTACCTTGG	161436
rs770529321	snp	C/T	0.000184689	0.00960784	intron-variant	EML5	GRCh38.p7	14:88662990	TTTTCTAGCCACTTT[C/T]ATTCACATGAACAAC	161436
rs770542158	snp	A/G	2.28037e-05	0.00337659	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618720	TCTTTGCAGTAGCTG[A/G]TTCTGTTAAGAGTGG	161436
rs770568209	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790285	GGAAACTTATTTTCA[C/T]TGTTATACATTAAAG	161436
rs770576628	snp	C/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88663038	TGTCCTACCTCCACG[C/G]TGGGGATGGTTTGTT	161436
rs770580575	snp	C/T	1.65622e-05	0.00287764	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688449	AGTGTGCCTATGTAG[C/T]CTTTTCTTCCAATCA	161436
rs770605175	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88694569	TTTGTCATCATTTTA[A/T]TATGGTAACTCTGCT	161436
rs770619694	snp	A/G	1.65787e-05	0.00287907	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88658244	AAGGCCTTTTTTCTC[A/G]ATAGCCTTCCATCTC	161436
rs770619723	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88698076	AACAAATAACACTGC[A/G]ATCAGCCAATATTTC	161436
rs770624293	in-del	-/G	2.67112e-05	0.00365443	intron-variant	EML5	GRCh38.p7	14:88687343	CTATGGAAAAAAAAA[-/G]GTTCAAGTTAATAAA	161436
rs770626689	snp	A/G	3.1066e-05	0.00394107	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715171	CTCCTTCCTATCTTT[A/G]ATATGTACAACTTCC	161436
rs770638403	snp	A/C	1.66615e-05	0.00288626	intron-variant	EML5	GRCh38.p7	14:88746176	GAAATCTCAAAAGAG[A/C]ATACTTACTCTATCT	161436
rs770653927	snp	G/T	1.70414e-05	0.00291898	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740402	AGCATGGGCTCCTTG[G/T]ATTGTTCGTATAAGA	161436
rs770659385	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88707257	TAAAAATCTATGTGA[C/T]AATAGGGATATATTT	161436
rs770667336	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88778210	AACTAAAATAAGACC[G/T]GAACGAAAGAAGGAA	161436
rs770673042	snp	C/T	1.68482e-05	0.00290238	intron-variant	EML5	GRCh38.p7	14:88685162	AATGTTAAATGAAGA[C/T]GTTCTTTTAGACATA	161436
rs770687631	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88745876	AAACCTCCATGGCAC[A/G]TGTATACCTATGTAA	161436
rs770719113	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692359	TCCAGCCTGGGCAAC[A/G]GAGCGAGACTCTGTT	161436
rs770732489	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88723844	ATGAAGAAAAGATAA[A/G]TTTTAAGAAGATATT	161436
rs770755944	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88683030	CTTCATTTACAGCAG[A/G]GTGTGAAAAAGCTCA	161436
rs770790183	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644105	ACTCTTTAATTTACA[A/G]ATTTAAGCCACTAAA	161436
rs770834351	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88736757	AGAACGTCTCTTCCC[A/G]TTTGGTGCACTTTCC	161436
rs770838865	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88735336	AATTTCTTTAATATA[A/T]AAACAGGTATCATTA	161436
rs770840275	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88681542	TTAGTTCTTTTTTGA[A/T]TTTTTTTTAGTCCCC	161436
rs770853435	snp	G/T	3.31494e-05	0.00407107	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685026	TTACCTGAACCAGAA[G/T]TGTTATTGGGCCACT	161436
rs770854021	snp	A/G	3.32094e-05	0.00407475	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616280	CTCAGGGCATTTGGT[A/G]CACACAGAAGTCAAA	161436
rs770859677	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88619406	TTTTTAAATAGAGGC[A/G]GGGTCTCACTATGGT	161436
rs770861735	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88781897	TTATTAGCAGTGTCA[A/G]AACGAACTAATTCAG	161436
rs770866986	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88635640	ATACCAATTTAGAAC[A/T]CCTTAGAGTTTGGGC	161436
rs770901729	snp	C/G	1.66081e-05	0.00288163	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88681929	ACATACAATGACTAG[C/G]TGAGAGATCCCATAT	161436
rs770927195	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88749153	CAAATTGCTGAAGCC[A/T]TCGCTAAAGGGCAAA	161436
rs770961828	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664594	TCTATAAAGCTGTCA[C/T]GGGATGCTACAGCAA	161436
rs770970082	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647119	TATAATCCCAGCACT[C/T]TGGGAGCCCAAGGCA	161436
rs770970198	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630489	TTTTATTCAGGAATC[C/T]ACTCCTTCCTAGAGC	161436
rs770974811	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88662542	CAAGTGATTTATTCC[-/T]TTTTTTTTTTTTTTT	161436
rs770986796	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783068	TGGGCAAGACAGAGT[A/G]AGACTCCATGTCAAA	161436
rs770994147	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88787080	TCAAATATTCTCTCA[C/T]AACACAAAACCACTG	161436
rs770995151	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88689742	CTGTCTCCAAACAAA[A/G]AGAGAGAGAGAGAAA	161436
rs771000873	snp	C/G/T	0.000452782	0.0150395	intron-variant	EML5	GRCh38.p7	14:88726530	TATGTGTTTCTACCC[C/G/T]AATACCATACCTTAC	161436
rs771000944	snp	C/G	3.73951e-05	0.0043239	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702555	CGATTATAAATGACA[C/G]CCACTGCTGCCACAT	161436
rs771001547	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88620456	AGATAGCTCTCTTGT[A/G]TTACAGTGGGAGATA	161436
rs771005489	snp	G/T	1.65688e-05	0.00287821	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621188	CCTGGAAGGATGTGT[G/T]GCTAGTCCCCAGATT	161436
rs771018548	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88775906	TTTAGGTGGCTCAGA[-/AG]AGAGAGAGAGAGAGA	161436
rs771045612	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88774803	GGCTTTAAATACTGT[C/T]TATATGCTGATAACA	161436
rs771064599	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88651158	TTGTCATTTTCTTTT[-/C]TTTTTTTTTTTTTTT	161436
rs771082022	snp	A/G	1.66043e-05	0.00288129	intron-variant	EML5	GRCh38.p7	14:88665495	CACCTCCCACCTGAA[A/G]GAGAAAGAGCATATT	161436
rs771095641	snp	A/G	0.000136323	0.00825488	intron-variant	EML5	GRCh38.p7	14:88620952	AAAAAAAAAAAAAAA[A/G]AGTCATAGGAAACAT	161436
rs771100704	in-del	-/G	1.6819e-05	0.00289987	intron-variant	EML5	GRCh38.p7	14:88625145	AAAAGGAGTGGGGGA[-/G]GGGGGAGACAAACTC	161436
rs771101805	snp	C/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792287	GCAGGGTGACGGCGG[C/G]GGCCCCCGCTCCCCG	161436
rs771109441	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88741518	TTAGGTAAATTTTTA[C/T]AGTTCACGGAGAGAA	161436
rs771121482	snp	A/C	1.7058e-05	0.0029204	intron-variant	EML5	GRCh38.p7	14:88644554	AGGCATGCAGCACTC[A/C]GTGCCTTCACTGAGC	161436
rs771121978	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88622041	CCCCTCCCCCTCCCC[A/C/T]TTGTCCGCCTCCAGT	161436
rs771123166	snp	C/G	3.48359e-05	0.00417334	intron-variant	EML5	GRCh38.p7	14:88638759	ATATTGAATTTATTT[C/G]AACAAAGCAAATGCT	161436
rs771133314	snp	C/T	1.69407e-05	0.00291034	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696873	ACGGCACTAACACCA[C/T]ACTGGTGGTGGCCCT	161436
rs771133579	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88738704	GAACCTAAACTCTTT[A/C]CAGGCAAAATTTCTC	161436
rs771183481	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88748619	AATGTGACTAATAAC[C/G]TGGGGAAAATCACTC	161436
rs771197818	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88666795	TTGGTATCTTGTATG[-/A]AATCTGATGAGGAAA	161436
rs771198448	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88789146	AAGGTATAGATGTGC[A/C]TCTTATGCTAAAACT	161436
rs771270712	snp	C/T	0.000138341	0.00831574	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792284	CTTGCAGGGTGACGG[C/T]GGCGGCCCCCGCTCC	161436
rs771280388	snp	G/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626364	TGGTGGCTCATGCCT[G/T]TAAACCCAGCACTTT	161436
rs771292214	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717077	GAGTTGATCAGAGCA[C/T]ACAACCGAAGAATCA	161436
rs771302758	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88657931	AAATATGAGGTTTAA[C/T]AATATAAAATTTACC	161436
rs771310551	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88786152	CATTACCTCACCTCC[C/T]AGTCTCTACTTAAGT	161436
rs771312614	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88650858	TGTTACCCAGGCTGG[A/T]GCTAAACACCTAGTC	161436
rs771323404	snp	C/G	5.49124e-05	0.00523958	intron-variant	EML5	GRCh38.p7	14:88618379	CCATTAGGTGAGAGA[C/G]AAAATCCACAGGGGG	161436
rs771324471	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780848	AAAGTGCTGGGATTA[C/T]AAGTGTGAGCCACTG	161436
rs771333779	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612725	TTACAGAGATCAGAT[C/T]AGATAGGTAAACTGC	161436
rs771355089	snp	C/T	1.65611e-05	0.00287755	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688315	GCCCATCATGCGCTT[C/T]CACTGTTTTTACAAG	161436
rs771356471	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88667083	GCTTGAGTGGTGATG[A/C]CATTTACTGAGATGG	161436
rs771387860	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703041	TGTAAGCCACCATGC[C/T]CAGCCTGAACAATTA	161436
rs771397054	snp	A/G	1.71e-05	0.00292399	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706265	ACTACTCACCTTGGG[A/G]TGCTATGTGAACAGC	161436
rs771438247	snp	C/T	1.69152e-05	0.00290814	intron-variant	EML5	GRCh38.p7	14:88625154	TGGGGGAGGGGGAGA[C/T]AAACTCATCAAAAGT	161436
rs771443720	snp	A/G	6.01739e-05	0.00548483	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738904	CTGGTCTGTTTCCCT[A/G]AGATCAATCACAGTA	161436
rs771456651	snp	C/G			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715128	CAAGGTAAGTTCCAT[C/G]TGGTGAATATTTTAA	161436
rs771464096	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88735150	GGTTCTCAAACTTTT[A/G]AGTATATCGTAGTCA	161436
rs771488484	snp	A/C/G	5.4087e-05	0.0052001	intron-variant	EML5	GRCh38.p7	14:88618375	AATTCCATTAGGTGA[A/C/G]AGACAAAATCCACAG	161436
rs771511793	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88713094	AGCGTCACAACAAAT[-/A]AAAGTACTATGCAGT	161436
rs771538225	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756241	ATATTAACAGAAGAA[A/G]GGTCAAAAAAACTCC	161436
rs771555700	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88726896	TTTTTGGCGACATCA[C/T]GTCACTCTGTCACTC	161436
rs771565559	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88682819	ATAATGGGGTCCTGG[A/G]GTAACCCAGGAAAAG	161436
rs771566672	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88632583	GGGTTTATGCAGGAA[A/G]GATTTAATATAAGCA	161436
rs771573793	snp	C/T			utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88614305	AGGAGAATCCACTGA[C/T]GAACAAGTACCAACT	161436
rs771576194	snp	A/G	1.67192e-05	0.00289125	intron-variant	EML5	GRCh38.p7	14:88625130	ACGTCAAGTTATTCT[A/G]AAAAGGAGTGGGGGA	161436
rs771576231	snp	A/G	3.31219e-05	0.00406938	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88688309	ACACTGGCCCATCAT[A/G]CGCTTTCACTGTTTT	161436
rs771580111	in-del	-/A			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	EML5, ZC3H14	GRCh38.p7	14:88615008	TTCTTTCTTCCAGTT[-/A]AATACTGTTGCTCCC	161436
rs771583214	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703363	GGTGGGAGAAAGATT[C/T]TCAAACTGTACCCTT	161436
rs771583902	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630299	CCTCCCAAAGTGCTA[A/G]GATTACAGGCATGAG	161436
rs771599073	snp	A/T	1.90271e-05	0.00308435	intron-variant	EML5	GRCh38.p7	14:88661862	ATGCTGTAAGTTTGG[A/T]TTATCCAAACCTAAA	161436
rs771614664	snp	A/T	1.65619e-05	0.00287762	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688424	ACACATCATTGTGTC[A/T]TTTTTCCCCAGTGTG	161436
rs771631908	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88728599	GTCTACATCCTCATC[A/G]TCTTCACATTGTGTA	161436
rs771643514	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88758173	CTTCTATAAATATAC[-/AT]ATATATATACATATA	161436
rs771684486	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88672078	TACAGAACTCTCCAA[-/C]CAAAAACAATAGAAT	161436
rs771689862	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88717417	TAATTTGTGAGGTTA[A/C]GCTAGGATAAGATGT	161436
rs771698547	snp	A/C			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615450	GAAACCATTTTGCTA[A/C]AAAGATAATGAAAAT	161436
rs771699234	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770668	AATGAAAGCATGAGT[A/G]TTGTTCAGGTATCCT	161436
rs771718828	snp	A/T	3.53463e-05	0.0042038	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705554	ATCAGACAGATCTGA[A/T]TCTGATTCATCACTA	161436
rs771735796	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88711056	CAACGTCTAAGAGGA[A/G]GATCATCATGACTAC	161436
rs771757390	in-del	-/A	0.000149196	0.00863571	intron-variant	EML5	GRCh38.p7	14:88688482	CTCCCCCTAGTTCAC[-/A]AAAAAATATTATGAA	161436
rs771758343	snp	A/G	1.66158e-05	0.0028823	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616173	CAGCACTAACAACAT[A/G]TCGATCACCACTGGT	161436
rs771778230	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757753	AATACAAATCAAAAA[C/T]CACAATAATATACCA	161436
rs771785208	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88671312	CCAAACTAAGCCTCA[C/T]AAGTGAAGGAGAAAT	161436
rs771807508	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88745428	TAAAAATAGTATAAT[-/A]TTTAATTAAAAGCTG	161436
rs771810485	in-del	-/ACAATTTTATATTAAAGT	1.7294e-05	0.00294053	cds-indel, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706361	AATAACCCACTGATA[-/ACAATTTTATATTAAAGT]ATCATGTGACCATCT	161436
rs771812544	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88718164	TCAGTTTGGGAGGGA[C/T]ATCATGAGTTCAGTT	161436
rs771818767	snp	A/G	6.94324e-05	0.00589164	intron-variant	EML5	GRCh38.p7	14:88743982	ATACTTAGCAGCAGA[A/G]AACTAAACGTGACTA	161436
rs771829669	snp	A/G	1.7709e-05	0.0029756	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702545	GTTTTGCTGTCGATT[A/G]TAAATGACACCCACT	161436
rs771853097	snp	C/T			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705512	GAGCTGTGTCTCTTG[C/T]TCAATTTCAGAATCC	161436
rs771882987	snp	C/T	9.44309e-05	0.0068707	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88715141	ATCTGGTGAATATTT[C/T]AACTCATGAATTGCC	161436
rs771886296	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88762511	GTGAAACTCCATCTC[A/G]GGGGAAAAAAAAAGA	161436
rs771910340	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88755586	ATTTCTATTTGATAA[-/T]TTTTTTCTATATGTC	161436
rs771955962	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88696421	AATTGTCACTGTATA[A/G]ATATGTCTAAAATAA	161436
rs771972689	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750114	CCACAAAGTTTAAAA[C/T]ATTTACTATTTCACT	161436
rs771979616	snp	C/G	2.07596e-05	0.0032217	intron-variant	EML5	GRCh38.p7	14:88642869	AAAAAATTGATAGAG[C/G]GATGGAGAATCAGGG	161436
rs771989713	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88748425	TGTCATACCTTAATA[C/G]TGAAATTATACCAGT	161436
rs771997966	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88711559	CACAACAGCAGCATA[G/T]AGGAAACTGCCCCCA	161436
rs772004444	snp	A/G	1.71502e-05	0.00292827	intron-variant	EML5	GRCh38.p7	14:88621369	TTCTTCATAATATAA[A/G]AATGACCCTATTGAC	161436
rs772026281	snp	C/T	1.79583e-05	0.00299647	intron-variant	EML5	GRCh38.p7	14:88702437	TTATTGTCAGTCTTT[C/T]AAACCTACCTGGCCT	161436
rs772042902	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780680	TCCCAGATTCAGGCA[A/G]TTCTTGTGCCTCAGA	161436
rs772053731	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660922	AAAAGTCATTCATTA[C/T]ATTAAATCAATGGTG	161436
rs772068287	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88775907	TAGGTGGCTCAGAAG[-/AG]AGAGAGAGAGAGAGA	161436
rs772079414	snp	C/T	1.66247e-05	0.00288307	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715029	GATGAGTGATGAAAC[C/T]AAGGGATCCCAAACA	161436
rs772081400	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788950	ATCTGTGGTCTCAGC[C/T]ACTTGGGGAGGCTGA	161436
rs772118241	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733997	TTTGCTTACCTAAAA[C/T]AACCTACACGAAGTA	161436
rs772136822	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668195	TCTTTTTATTAAATT[C/T]CCACTGTTCAAATAA	161436
rs772152070	snp	A/G	2.21246e-05	0.00332593	intron-variant	EML5	GRCh38.p7	14:88620744	AACTCTATTCCATTT[A/G]TTCACTAACCTGATA	161436
rs772160577	snp	C/G	3.0453e-05	0.003902	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627807	TCCCAGATGTGAATA[C/G]AAGGAGCTGTAGCTA	161436
rs772171016	snp	G/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620851	CATTTTTCATTCCAA[G/T]AGCCACCATGTCCCC	161436
rs772177378	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88786927	ATGATGAAAAATCAA[A/T]TAAGATGAGAACTGA	161436
rs772177794	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88702677	AATTTTGGCCTTTTA[G/T]CTGATCAATACAGAA	161436
rs772207780	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88689699	TGATTGTGCCAGTAC[A/G]CTCCAGCCTGCGTGA	161436
rs772209475	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88650695	CATAGCTGGAGTGCA[A/C]GGGTGCGATCATAGC	161436
rs772216291	snp	A/G	1.93104e-05	0.00310722	intron-variant	EML5	GRCh38.p7	14:88712235	GAAAGTCTTCTGTGA[A/G]AGAGAGGTTACTTAA	161436
rs772227752	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691984	AAACAAATTCATAGT[C/T]CTTTTCCAAGACAGA	161436
rs772231086	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88688147	AAAGGTCAAGATGAC[C/T]CTAGCCCACAGACTA	161436
rs772242051	snp	G/T	1.67153e-05	0.00289091	intron-variant	EML5	GRCh38.p7	14:88627093	TTACAAGAACCAAGC[G/T]AATCAACAGCATCAA	161436
rs772244726	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88722880	CAAACCTGCACATTC[C/T]GCACATGTACTTTGT	161436
rs772256554	snp	A/G/T			intron-variant	EML5	GRCh38.p7	14:88635593	AGCCTCTTACCTTGA[A/G/T]GAGTACACTCCTATA	161436
rs772265450	snp	A/G	2.12213e-05	0.00325733	intron-variant	EML5	GRCh38.p7	14:88695464	CATCCGCTGTGGAAA[A/G]TTAATGAGAGAGATA	161436
rs772267915	snp	A/C	3.31411e-05	0.00407056	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658308	GCCTAGGGTAACCAA[A/C]ATGCTGTCATCATAA	161436
rs772301117	snp	A/G			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738952	ATCCCAAAGACGAAT[A/G]CAACCATCTCTGCCA	161436
rs772302728	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755002	TAGAGATGGGGTTTC[A/G]CCACATTGGCCAGGT	161436
rs772309596	snp	A/G	0.000182226	0.00954358	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740491	CCCTTGCACAGGCTA[A/G]GCACAGTATTGTCTG	161436
rs772314985	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761731	ATGGGATTCTTGGGT[C/T]AAACGGTATTTCTGG	161436
rs772326336	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779008	TTAGATTGTAGATTG[C/T]ATATGTGAGAATTTT	161436
rs772328180	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774447	TTTTGTGTACCAATA[A/G]TGACATGACTCATTT	161436
rs772389576	in-del	-/TTG			intron-variant	EML5	GRCh38.p7	14:88727039	CAACCTGGCTATGTT[-/TTG]TTGTTGTTGTTGTTG	161436
rs772403282	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88729183	ACACATACATATATA[A/T]GCTATACACATATAC	161436
rs772431160	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639873	GGCATGAGCCACCGT[A/G]CCCAGCAGGAATTGA	161436
rs772442588	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88626308	GGCTTTTGAGTATAA[C/T]AGTAGTCCAAGGAAT	161436
rs772442884	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674052	GGTGGGCGGATCACT[C/T]AATATCAGGAGTTCA	161436
rs772449826	snp	A/G	1.6591e-05	0.00288015	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625028	TGGTGTACATGGCAA[A/G]CACAGGCCCGTTGTG	161436
rs772451455	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88789305	AGAACAAAAAAGTGA[-/C]CCCCAAAAGCCCTAT	161436
rs772469619	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88674528	CACAGGAAAGACCCG[-/C]CCCCATGATTCAATT	161436
rs772474535	snp	A/G	5.16427e-05	0.00508121	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696860	ACCTGAGAAATCAAC[A/G]GCACTAACACCATAC	161436
rs772477833	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88678431	CTGCACATGTATCCC[A/G]GAACTTAAAATAACA	161436
rs772481460	in-del	-/GAGTT			intron-variant	EML5	GRCh38.p7	14:88751614	CAAGTGTGATATTTA[-/GAGTT]GAGTTGAGAAGCCAG	161436
rs772484171	snp	C/T	1.66156e-05	0.00288228	intron-variant	EML5	GRCh38.p7	14:88705469	AGAAAAACCATGTGA[C/T]ATGGAAAATTACCTG	161436
rs772489145	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666894	CATACATTGGAAATG[A/G]AGAAATCTAAGATGT	161436
rs772489969	snp	A/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765693	CAGGAATTAGAGTAT[A/G]GATATCTTTGGGGCC	161436
rs772493646	in-del	-/AAAAAAA/AAAAAAGA			intron-variant	EML5	GRCh38.p7	14:88660762	AAAAAAAGAAAAAAG[-/AAAAAAA/AAAAAAGA]AAAAAAAAAACTTAA	161436
rs772496199	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88639373	GTCATGAAGAAGAAA[A/G]ATGAGTAACATGGTT	161436
rs772508974	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88757134	AGGATATGCAGATCA[A/G]TCAAACAGAATCGTG	161436
rs772518655	snp	C/G	2.23396e-05	0.00334205	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615802	AAGTTAATTTCTGTA[C/G]TCATCTCAGCATCTC	161436
rs772523825	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88636586	GAATGGCGTGAACCC[A/G]GGAGGTGGGGGCTGC	161436
rs772529789	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769679	CTCAACTAGGAAATA[C/T]AGTTATGTATACTAA	161436
rs772539186	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88665610	GGCAGGAGGACTGCC[C/T]GCGGCCAGGAGGTTA	161436
rs772540269	snp	A/T	1.92821e-05	0.00310495	intron-variant	EML5	GRCh38.p7	14:88661865	CTGTAAGTTTGGATT[A/T]TCCAAACCTAAAGTA	161436
rs772543192	snp	C/T	1.65864e-05	0.00287974	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88736555	CCAACACACACTCCT[C/T]ACAGACAAACCTAGT	161436
rs772582314	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88715810	TGGGATTACAGGTGC[A/G]CACCACCATACCCGG	161436
rs772583600	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88738355	TTTAAACACAAACCT[C/G]TGGGTAGCTTTTATA	161436
rs772600356	snp	A/C	0.000839983	0.0204765	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792518	TGTCGGGGCGCCCAC[A/C]CGCCGCTCCCGCTCG	161436
rs772614235	snp	A/G	1.68764e-05	0.00290481	intron-variant	EML5	GRCh38.p7	14:88644540	GTGGGGAGGAGGAAA[A/G]GCATGCAGCACTCAG	161436
rs772669136	snp	A/G	4.99463e-05	0.00499707	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644437	GTTTTCCTTACCTCT[A/G]TAGGTCTCTTTTTCT	161436
rs772669228	snp	A/G	1.65825e-05	0.00287941	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88665452	GAGACCTACGGCTAA[A/G]GCTTTACCATCAGGA	161436
rs772703320	snp	A/G			downstream-variant-500B, utr-variant-3-prime	EML5, ZC3H14	GRCh38.p7	14:88614417	GGTTATGCTTTCTGT[A/G]ATGTAATTTAGTCAT	161436
rs772717852	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88757766	AATCACAATAATATA[C/T]CATTTCTTTTTTTCT	161436
rs772720315	snp	A/T	1.65693e-05	0.00287826	intron-variant	EML5	GRCh38.p7	14:88665319	TTAATACTCAAATAC[A/T]ATTTCAATGGATCTT	161436
rs772746886	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88753951	TGAGACCAGCCTGGG[C/T]ACCACAGTGAGATCC	161436
rs772769141	snp	A/G	4.99289e-05	0.00499619	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618269	GTCAATAGCGGCATG[A/G]TCCATAAGATGTTTT	161436
rs772771829	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88630408	TGTCCTTTAGTCTCT[C/G]TAGTGAGTAACTCCT	161436
rs772787587	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690836	TAGTGCACAAATGGA[A/G]GAACTGGCCTTTATT	161436
rs772800324	snp	A/G	3.32624e-05	0.004078	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715031	TGAGTGATGAAACTA[A/G]GGGATCCCAAACACT	161436
rs772831734	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88728608	CTCATCATCTTCACA[C/T]TGTGTAGGCTGAGGA	161436
rs772835510	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88756524	CCAGGAAAAGGAACA[A/C]AAAGTAAAAGTAAAG	161436
rs772868094	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653112	GTCTATTATTGGTGT[A/G]GAGGAATGCTTGTGA	161436
rs772878985	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88727099	GTTATAGTGTCACTG[A/C]ATAATAAACACAATG	161436
rs772914110	snp	A/T	1.67624e-05	0.00289498	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88661750	AGCAGTTACATCTGT[A/T]ACTTCTCCAATTACT	161436
rs772925024	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762530	GAAAAAAAAAGAAAC[C/T]TACAAAGAGATTTAG	161436
rs772974012	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88663204	TTTAAGTTTTATGGG[-/A]AAAAAATCAGCTTAA	161436
rs772979136	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88644049	CCCTGTACAGTGAAT[A/G]TATCGCACAGGGTCA	161436
rs772980115	in-del	-/TGGGCTAGCTCT			intron-variant	EML5	GRCh38.p7	14:88632668	GAAGGGCCTGCTTGC[-/TGGGCTAGCTCT]TGGCCAGTGTGTAAG	161436
rs772981467	in-del	-/AGA	3.00359e-05	0.00387518	cds-indel, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627806	ATCCCAGATGTGAAT[-/AGA]AGGAGCTGTAGCTAA	161436
rs772992748	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88705782	CCTCTCCACTCACTG[A/C]AAACTCAATAGCTCC	161436
rs772993989	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88747583	TAACATAAGCTTAAC[A/G]TGAGAAATAAGCTTA	161436
rs772997856	snp	A/G	1.66128e-05	0.00288204	intron-variant	EML5	GRCh38.p7	14:88685003	AAAAAACAAATTAGC[A/G]TTTAAAATTACCTGA	161436
rs773007089	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88637072	AACATTGTAAATGCT[A/G]TTTTGTGTTTTGTGG	161436
rs773012172	snp	A/G	2.30587e-05	0.00339541	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88738976	TCTGCCACCAGTAGC[A/G]AAGCCTTCTTCACAA	161436
rs773032291	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88628718	ATGCAGAAATAAATG[C/T]TGGTCTCTAAAGAAA	161436
rs773034486	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88642356	CTGAATAACCCAATC[A/T]GTTAAATGAACATCA	161436
rs773042283	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88742928	TAATTAATTCACTAG[A/G]AATTAACTGTTACCA	161436
rs773046662	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768298	GTATGCTAGGGGAGA[C/T]ACTGTGAGACTATGC	161436
rs773054748	snp	G/T	2.01193e-05	0.00317163	intron-variant	EML5	GRCh38.p7	14:88642874	ATTGATAGAGGGATG[G/T]AGAATCAGGGTTTCC	161436
rs773065004	snp	G/T	3.4901e-05	0.00417723	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702449	TTTCAAACCTACCTG[G/T]CCTGTTGCCACGTAG	161436
rs773065950	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88681734	ACTGAGTACAATTAC[A/G]TTTCTCTATGTGGCA	161436
rs773066511	snp	C/T	6.89679e-05	0.0058719	intron-variant	EML5	GRCh38.p7	14:88743990	CAGCAGAGAACTAAA[C/T]GTGACTATTATAAAA	161436
rs773077226	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88668716	TTCTGCTGGTTGGGT[A/G]CAGGCATAAAGCAGG	161436
rs773181076	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88780685	GATTCAGGCAATTCT[A/T]GTGCCTCAGACTCCC	161436
rs773182857	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88673804	AGAATAAAATACCTA[C/G]GAATATAGTTAACAA	161436
rs773185171	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88650227	GGAGGCTGAGGTGGG[C/T]GAATCACTTGAGGTC	161436
rs773188127	snp	C/T	1.77637e-05	0.00298019	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702546	TTTTGCTGTCGATTA[C/T]AAATGACACCCACTG	161436
rs773241934	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88646690	ATAAGGTATATCATT[G/T]CTGAAAATAAAATTA	161436
rs773269097	snp	C/T	8.74898e-05	0.00661342	intron-variant	EML5	GRCh38.p7	14:88621380	ATAAAAATGACCCTA[C/T]TGACCTGCTTTCAGA	161436
rs773298178	snp	C/T	2.14089e-05	0.0032717	intron-variant	EML5	GRCh38.p7	14:88695466	TCCGCTGTGGAAAAT[C/T]AATGAGAGAGATAAA	161436
rs773306029	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88781719	TAAAGGGCTTTTCCC[C/G]CTCTTCACTCTGCAC	161436
rs773314616	in-del	-/ACAAG			intron-variant	EML5	GRCh38.p7	14:88720714	CCCTTGAAAACTGGC[-/ACAAG]ACAAGGATGTCCTCT	161436
rs773315908	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88619142	AAGCGGAGGCGGGCA[C/G]ATCACCTGAGGTCGA	161436
rs773317581	in-del	-/TAAAT			intron-variant	EML5	GRCh38.p7	14:88666640	TTTTATTATTAATGA[-/TAAAT]TAATATCGTTCATTA	161436
rs773319417	snp	G/T	0.00619795	0.0553223	intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88792278	GAGCGGCTTGCAGGG[G/T]GACGGCGGCGGCCCC	161436
rs773322092	snp	C/T	0.000103461	0.00719164	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620923	TCACTTTGTTTAACA[C/T]CTTCTGCATTTAAAA	161436
rs773348408	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88773691	ATTTCTTTGGGTAAG[G/T]CTTGGCCATTGGTGG	161436
rs773359380	snp	C/T	2.27472e-05	0.0033724	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665348	TTACCAGGTGAAAAT[C/T]GAATATCTGAAATCA	161436
rs773367414	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88733526	ACTTTTTAAAGAAAC[A/C]ATTGTCCTATTGGCA	161436
rs773399657	snp	A/C	1.66015e-05	0.00288105	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627809	CCAGATGTGAATAGA[A/C]GGAGCTGTAGCTAAA	161436
rs773400194	in-del	-/CATAGT	6.66189e-05	0.00577105	intron-variant, cds-indel	EML5	GRCh38.p7	14:88616105	TCTCTTAACTAGTAA[-/CATAGT]CTGCTCTTCATGGGC	161436
rs773411722	snp	A/G	2.02407e-05	0.00318118	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620764	CTAACCTGATATCAT[A/G]GATTGCACATCTCCT	161436
rs773420953	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665636	GGTTAAGACCAGCCC[A/G]GGCAACATAGCAAGA	161436
rs773428118	snp	C/T	1.92036e-05	0.00309862	intron-variant	EML5	GRCh38.p7	14:88627616	TGTATTCTTGTTTTT[C/T]TAAAAATCAAACACA	161436
rs773443716	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625502	TGCTTCCCAGGTTCA[A/G]GTGATTCTCCTGTCT	161436
rs773444490	in-del	-/TTT			intron-variant	EML5	GRCh38.p7	14:88764837	GTTCTGTGTTACTGA[-/TTT]TTATTTTGATTCCAT	161436
rs773444668	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88774582	GTCCTCATCTTATTG[A/G]ACACAGCTGATAATT	161436
rs773451401	in-del	-/T	3.42214e-05	0.00413637	intron-variant	EML5	GRCh38.p7	14:88620931	TTAACATCTTCTGCA[-/T]TTTAAAAAAAAAAAA	161436
rs773459910	snp	A/G	1.66032e-05	0.0028812	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736560	ACACACTCCTTACAG[A/G]CAAACCTAGTAAAAA	161436
rs773469536	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88645142	CAACTCTTGTGCCTC[-/A]AGCCTTCCCAGTAAC	161436
rs773480628	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88723075	CCTAAGTGTCCATCA[A/C]TGTACACATGAATAA	161436
rs773497471	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778677	CCAGCTACTCAGGAG[A/G]CTGAGGCAGAGGAAT	161436
rs773498602	snp	A/G	0.00011612	0.00761882	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625038	GGCAAACACAGGCCC[A/G]TTGTGAGCTCTCGCC	161436
rs773512579	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88674141	AGGCATGGTAGCGCA[G/T]GTCTGTAATCTCAGC	161436
rs773517917	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88729262	AATGGTGAAAATAGC[A/G]TAACTGTCTTTTTTC	161436
rs773519142	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88683215	AATATAGGCTAAACC[A/G]TAGGCCAGCTAGTTT	161436
rs773523848	snp	C/G	2.04581e-05	0.00319822	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695364	TTTTTTTCCTACCTT[C/G]CTATTGAAAGTTTCT	161436
rs773528568	snp	A/G	3.75749e-05	0.00433429	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705569	ATCTGATTCATCACT[A/G]TGAGAGTCAGCCAGA	161436
rs773530413	in-del	-/C	3.5957e-05	0.00423995	frameshift-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88726661	CTATTAATGCATGAT[-/C]CTACTAGGCTCCATA	161436
rs773534038	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711062	CTAAGAGGAAGATCA[C/T]CATGACTACTACTGA	161436
rs773568102	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710285	TCATATGATCATTCT[C/T]TCTTTGAGCTAACTT	161436
rs773573188	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88714390	ACTGGGAGAGGTAGA[C/G]GTTGGTGGGGGCCGG	161436
rs773672467	snp	C/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88793509	CTCCGGAGTAGTAAG[C/G]AGTACAGTTGCGTAC	161436
rs773682003	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88679565	GCCGTGGTGGCGCAC[A/G]CCTGTAGTCCCTGTT	161436
rs773686771	snp	A/G	1.706e-05	0.00292057	intron-variant	EML5	GRCh38.p7	14:88743974	TGCAATATATACTTA[A/G]CAGCAGAGAACTAAA	161436
rs773724051	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88667003	TTTGGATATATTTCA[A/C]AGATAGAGCTGGCAG	161436
rs773764807	snp	G/T	1.70235e-05	0.00291744	intron-variant	EML5	GRCh38.p7	14:88622747	CAAGCCAGAGTAAGT[G/T]TTCATTATTGGCTAC	161436
rs773825223	snp	A/G	1.6996e-05	0.00291508	intron-variant	EML5	GRCh38.p7	14:88644548	GAGGAAAGGCATGCA[A/G]CACTCAGTGCCTTCA	161436
rs773834442	snp	A/G	3.31351e-05	0.00407019	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736374	CTTACCTGACCGAAC[A/G]ATCATCACTTCCAGT	161436
rs773861001	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748359	CCAGAATGAAGATAC[C/T]TCTTTGAACTCGCTG	161436
rs773876993	snp	C/G	1.69301e-05	0.00290942	intron-variant	EML5	GRCh38.p7	14:88622739	TAAATAACCAAGCCA[C/G]AGTAAGTGTTCATTA	161436
rs773880278	snp	A/G	1.66297e-05	0.0028835	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88644441	TCCTTACCTCTATAG[A/G]TCTCTTTTTCTTGCC	161436
rs773884510	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612672	TTGAAATGTAAAAAT[C/T]AGATTTAAATAGTAT	161436
rs773892136	snp	C/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88613195	GAAAGGCTTGAAACA[C/T]GAGAAGCAGCAAAGA	161436
rs773894245	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88628033	AATATATAGAACACT[C/T]CTTCAGGCCATATTC	161436
rs773920162	snp	G/T	1.66857e-05	0.00288835	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88740540	AAAGACACCTCGTTT[G/T]GGGGTCAGAGCATTT	161436
rs773920770	snp	A/C			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88768076	TAGAAAATGTCTCCA[A/C]ATTTGGATTTGTCAT	161436
rs773921685	snp	A/C	3.04372e-05	0.00390099	intron-variant	EML5	GRCh38.p7	14:88687213	CACTAAGTCTCAAAT[A/C]ACCTTTAGATCCTGG	161436
rs773928468	in-del	-/GGATATTATTGAGTTTATTGAG	0.000107187	0.00731997	intron-variant	EML5	GRCh38.p7	14:88663144	ATTTTTAAAAATATT[-/GGATATTATTGAGTTTATTGAG]TACACATATAAAATA	161436
rs773935431	snp	A/T	1.6596e-05	0.00288058	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658367	TATGGGCCACATACC[A/T]CTTAAACTTTCCAAA	161436
rs773938869	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88681596	GTTCTAAATTATGTA[C/T]AATCCATAGTCACAA	161436
rs773967896	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88755659	CACACCTGGCATCAC[A/G]GTGGAGAATCACTAA	161436
rs773973817	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88769313	GAGATCTCCCCACCT[C/T]GCTTCCTTCTACTCT	161436
rs773975809	snp	A/C	1.66197e-05	0.00288263	intron-variant	EML5	GRCh38.p7	14:88616904	AGGAACAAAAGAAAA[A/C]TCATCATGGCAAGTG	161436
rs773997015	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668582	ATGGAGCTACTGTCA[C/T]GTGAACACACAGAGA	161436
rs774010114	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654743	ATGTGGTGCTGAGAA[A/G]AATGTATATTCTGTT	161436
rs774016455	snp	G/T			utr-variant-3-prime, downstream-variant-500B	ZC3H14, EML5	GRCh38.p7	14:88614020	AAGGACAGAAATGCA[G/T]TGGAAACAGTTTTAT	161436
rs774038296	snp	G/T	1.66004e-05	0.00288096	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625005	CACGATAAGTCCATC[G/T]CGCAGGGTGGTGTAC	161436
rs774046125	snp	A/T	2.47265e-05	0.00351605	intron-variant	EML5	GRCh38.p7	14:88687336	CAAACCCCTATGGAA[A/T]AAAAAAGGTTCAAGT	161436
rs774052019	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703206	AGTATAATATTAAAA[C/T]TGTATACTATAAAAC	161436
rs774063209	snp	G/T	1.67209e-05	0.00289139	intron-variant	EML5	GRCh38.p7	14:88665524	TTAGGCAATTTTCCC[G/T]TTTTTCTAATTTAAA	161436
rs774070914	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88761528	CAAAGGACATGAACT[C/G]ATCCTTTTTATGGCT	161436
rs774101164	snp	C/T	2.49728e-05	0.00353352	intron-variant	EML5	GRCh38.p7	14:88705025	TAGAATATATACTAA[C/T]AAAGGTGTTCGTATA	161436
rs774125800	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760214	TTTGTTTTATGGACC[A/G]TGCTTTTGCTTAACC	161436
rs774141030	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88710028	CATTATTAACAGTGA[A/T]GGAGGTGATGGGCTA	161436
rs774148487	snp	A/T	2.29988e-05	0.003391	intron-variant	EML5	GRCh38.p7	14:88621093	TTGTAACCTCTTTTA[A/T]AAAAATTATCTGTAC	161436
rs774162715	snp	A/G	4.70113e-05	0.00484803	intron-variant	EML5	GRCh38.p7	14:88657532	TACGAGTAATTCTTT[A/G]AGCAATAACTGAGAT	161436
rs774163169	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88641903	ATTCCTTTCTTGTTT[A/T]TCTTACTCTTCCTCA	161436
rs774181311	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766707	CCCACACCCTATTCG[C/T]ACACTCCCTCCCCTT	161436
rs774189173	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88618965	GATCATGTATACTGA[A/G]ATTGTCTGGGTTACA	161436
rs774189679	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779311	TATCAGAAGTTTAAA[C/T]ATAGCACAGAAATAT	161436
rs774212912	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88651008	ACTAAAAAGCAATTA[C/T]TTAAATAAACCATGA	161436
rs774219045	in-del	-/TTAATAAAGATCTAAATATTTT	0.000158541	0.008902	intron-variant	EML5	GRCh38.p7	14:88687351	AAAAAAAGGTTCAAG[-/TTAATAAAGATCTAAATATTTT]TTAAAATAGTAACCT	161436
rs774247594	snp	C/T	1.65616e-05	0.00287759	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621219	GGCCCATCCACATGA[C/T]CGTTAACTAAAATAT	161436
rs774252491	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88673852	TTCAAAAACTACAAA[C/T]CACTGCTCAAGGAAA	161436
rs774257756	snp	C/T	3.36151e-05	0.00409957	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696916	ATGGTTTAATGGTCT[C/T]TGTATCCCATATATG	161436
rs774261844	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88710992	ACTAAGAAGATTAAA[C/G]CATTTTTGTTTTTGC	161436
rs774263721	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88693695	TAATTTTAGATTTCC[A/T]GAAAAGATGCAAAAG	161436
rs774275358	in-del	-/ATG	1.90645e-05	0.00308738	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626792	ATCTAAGGCAAGAGA[-/ATG]TAAAGTAGTCAAAGT	161436
rs774297080	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88640431	TACGTAAAAATTAAA[C/T]AACTTGCTCCTGAAT	161436
rs774307893	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88737252	GGCAGGACTGAAAGA[A/G]CTATTAACATGCTGT	161436
rs774309978	snp	G/T	3.87342e-05	0.00440063	intron-variant	EML5	GRCh38.p7	14:88712225	GCAAGAACACGAAAG[G/T]CTTCTGTGAGAGAGA	161436
rs774331678	snp	C/T	1.66114e-05	0.00288192	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715016	GAAGACCAGTCCAGA[C/T]GAGTGATGAAACTAA	161436
rs774332080	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88675040	TGTGGTTTTGCAGAG[C/T]ATAGCCCCCTTCCTG	161436
rs774342307	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88746652	GAAACCTGGAGGATG[A/G]GAAAACACCTACACC	161436
rs774342834	snp	A/C	3.62325e-05	0.00425617	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618789	CTAGAACCTACTGCC[A/C]GATACCGGGAATCCG	161436
rs774379286	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88705666	AAAAATTAATGATTA[A/C]GAGCTATGTCAGTTG	161436
rs774394248	snp	A/C/T	4.48654e-05	0.00473615	intron-variant	EML5	GRCh38.p7	14:88754470	TTTTCTATAATATAC[A/C/T]TTAACATACAATTTA	161436
rs774398300	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88632245	CCCCATATTTGTCTC[A/G]TTCTCTCCACATTCA	161436
rs774403623	snp	A/C	7.30647e-05	0.00604376	intron-variant	EML5	GRCh38.p7	14:88638798	TTTCTTTTTAAAATA[A/C]AGAAACATACCTACT	161436
rs774404537	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88783239	ACAAATGTGGGGTTG[C/G]ATCCCCTACACAGCT	161436
rs774428906	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88720575	TTTGATAAAATTCAG[C/T]ATCCTTTCATGTTGA	161436
rs774451260	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617489	AAAAGTGCTACTTGG[C/T]TGGGTCCAGCAGCAC	161436
rs774454788	snp	C/G	3.37815e-05	0.0041097	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661717	AGCTAGAACCATTTT[C/G]TCACTGGTGAGGCAA	161436
rs774456870	snp	A/G	7.86071e-05	0.00626876	intron-variant	EML5	GRCh38.p7	14:88627857	AGTTGTAATCTACCT[A/G]TTATAAATATTTCTG	161436
rs774461516	snp	A/G	1.66878e-05	0.00288853	intron-variant	EML5	GRCh38.p7	14:88627084	TCTAGGTTATTACAA[A/G]AACCAAGCTAATCAA	161436
rs774515687	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773096	AGGCACTATGTTTTA[C/T]TTGATCTTTTAACAA	161436
rs774532479	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88752232	TCAGCAATGCAATAT[A/G]TTACATTTAGAAAGG	161436
rs774534611	snp	C/T	3.46446e-05	0.00416186	intron-variant	EML5	GRCh38.p7	14:88695329	AAGTAATTCTAGTAT[C/T]TTGCAAATGTGATAT	161436
rs774549404	snp	A/C	1.65666e-05	0.00287802	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626916	TTTTTTGCTAAGAAG[A/C]GCTCTTCCTGCCAGG	161436
rs774581969	snp	A/T	2.4412e-05	0.00349362	intron-variant	EML5	GRCh38.p7	14:88657547	AAGCAATAACTGAGA[A/T]CAATTATGATCTTAT	161436
rs774593525	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88685725	AAAGTGTTGGGATTA[C/T]AGATGTGGGCCACCA	161436
rs774627271	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88738876	CATTTGTTTTGTTAT[C/T]ACCTTTGTATCCCTG	161436
rs774636023	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88707608	AGCCCCATCAACGAA[A/C]TTCTGGAGAAAAACT	161436
rs774658383	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88772667	CTGAGGCAGAAGAAT[C/T]GCTTGAACCTGGGAG	161436
rs774714862	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727148	TAACAGTAAAGTCCA[C/T]GCTCCACTTTGCCTT	161436
rs774723486	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790246	TGTATGATTCAGATT[C/T]TACTCCCTCATTGAA	161436
rs774738767	snp	C/G	3.31983e-05	0.00407407	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616259	TAAAAAACAATGACA[C/G]ACAAGCTCAGGGCAT	161436
rs774771471	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88688109	TTCATTCTGTGTTCG[G/T]GAGTTTGAAAAGAGA	161436
rs774778480	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88664030	TGCCTATAATCACAG[C/T]ACTTTGGGATGCCAA	161436
rs774807522	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88692319	GAGGTGGAGGTTGTA[C/G]TGAGCCGAGATCACA	161436
rs774839257	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88638627	CAACTCAGATAACCA[C/G]AGTGAGTGAGAGAAA	161436
rs774845375	snp	A/G			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622541	CTGCAAAGGGTGAGG[A/G]AATCACAGTAATAAC	161436
rs774846190	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88777881	TCAGGAGGCTGAGGT[A/T]GGAGGGTCACCTGAG	161436
rs774862548	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88678366	GATGGGTTGACAGGT[A/G]CAACAAGCCATCATG	161436
rs774893989	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88623979	CCTTTATGTAAAAGG[C/G]ACAAATTCTGCGCTT	161436
rs774905086	snp	A/G	1.83115e-05	0.00302579	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754616	AAATACAAATATAAG[A/G]CTCTTTCCCAACTTG	161436
rs774921886	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88713184	ATCACTGAAGGTCAG[A/G]AGTTCAAGACCAGCC	161436
rs774926477	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	EML5	GRCh38.p7	14:88792560	GCGACGGGAGGCGGC[C/G]GCGGCCCGGCAACGA	161436
rs774937073	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88783080	GTGAGACTCCATGTC[-/A]AAAAAAAAAGAAAAA	161436
rs774955942	snp	G/T	1.67818e-05	0.00289665	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740413	CTTGTATTGTTCGTA[G/T]AAGATTGATTCCTTT	161436
rs774958360	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88640181	AACAAAGAAATTCTG[C/G]ACTTGAATTCAATAC	161436
rs774974736	snp	C/T	1.66233e-05	0.00288295	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88664579	ATTACATTGTATATA[C/T]CTATAAAGCTGTCAT	161436
rs774998373	snp	A/C	3.45012e-05	0.00415324	intron-variant	EML5	GRCh38.p7	14:88665290	TGATACATTTATACA[A/C]TGCCAGACCCAAGTT	161436
rs775000068	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88731020	TTTAACTAACCACTT[A/T]CAGTTCTGTGAATTT	161436
rs775016966	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625357	GCTAGAATAACCTTA[A/G]ACAATTCTTCCCTTC	161436
rs775017373	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88779084	GTAATCACTGCTCCA[C/T]TAGTCTGTGTTCAAG	161436
rs775018616	snp	C/T			intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88626370	CTCATGCCTGTAAAC[C/T]CAGCACTTTGGGAGG	161436
rs775020892	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88714153	GCAAAGTTTATTTGA[-/T]GATAAACACAAAAAA	161436
rs775025417	snp	C/T	1.68397e-05	0.00290165	intron-variant	EML5	GRCh38.p7	14:88622728	TTTGACCTAAGTAAA[C/T]AACCAAGCCAGAGTA	161436
rs775042962	snp	C/T	5.46135e-05	0.0052253	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702602	AATTTGAGTATAAAA[C/T]AGATTACTTCGACAG	161436
rs775053010	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88716259	AAATAGAAAAATGAG[C/T]CCCAAGATAAATCCA	161436
rs775058704	in-del	-/TACTT			intron-variant	EML5	GRCh38.p7	14:88618864	ATGAAGTATTATAAA[-/TACTT]AAGATCAGTGACTTT	161436
rs775073941	snp	G/T	0.000126971	0.00796676	intron-variant	EML5	GRCh38.p7	14:88687187	AATCTTTTTTTCCTA[G/T]ACAAAAACCCCACTA	161436
rs775076576	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88682662	TTCCAGGTAGGGCAG[G/T]ATGTCAGCATTTCTC	161436
rs775084938	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88641335	AGGCCAATATTCCCA[C/T]AGAAAACTACAAAAC	161436
rs775096739	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88746130	AAATCTCCTGAACTC[C/T]CTTCTGGTCTTTCCC	161436
rs775099616	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88693450	CTCATGAGACGTATT[A/C]ACTTCCACAAGAACA	161436
rs775108935	in-del	-/T	8.29414e-05	0.00643924	intron-variant	EML5	GRCh38.p7	14:88688489	CTAGTTCACAAAAAA[-/T]ATTATGAAAGTACCA	161436
rs775113714	snp	C/G	1.66885e-05	0.00288859	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88622620	TTGCCTCTGCACACA[C/G]AACGAACACAATCTG	161436
rs775142256	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780356	GAAAAATAAAGATAA[C/T]ATCTCCCTCTGCACA	161436
rs775150453	snp	C/T	1.66582e-05	0.00288597	splice-acceptor-variant	EML5	GRCh38.p7	14:88643023	CTCCAACACAAGGTC[C/T]TATAATGATAATAAT	161436
rs775164154	in-del	-/AAAC	0.00128921	0.0253563	intron-variant	EML5	GRCh38.p7	14:88706456	TATCTTTAAATTGAT[-/AAAC]AAATGCTAAACAAAA	161436
rs775169290	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625563	CCAGCCACCACGCCC[A/G]GCTAATTTTTGTATT	161436
rs775176010	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88686757	TCAAGGTTTCAGTGA[A/G]TTATGATTGCACCAC	161436
rs775181206	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88749737	AGTGTCAATAAATTT[A/T]AAAAAATTAAAATAC	161436
rs775192812	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88751967	TATTCCAAAGGGTTG[C/T]TGGGAGGATTAAATG	161436
rs775206800	snp	A/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712455	ATGAACACCTTTTAT[A/T]TCTTCTGTACTTGTC	161436
rs775213396	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88736948	CAGACTCAGCCATAT[C/T]TGGGGACTGCCCACC	161436
rs775218856	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88772494	CGGACGAGGTAGCTC[A/G]TGCCTGTAACAGCAC	161436
rs775221812	snp	A/G	1.73573e-05	0.00294591	intron-variant	EML5	GRCh38.p7	14:88714904	TAAAATATTGTATAG[A/G]TACTACAAATCTATA	161436
rs775231092	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88672614	ATGAATCCAGGGGCC[A/G]GTTTTTGAAAAAAAT	161436
rs775251046	snp	A/G	2.89256e-05	0.00380289	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88726558	TACTCTAAGTACAGT[A/G]AATGAGCCATCCTTC	161436
rs775273383	snp	A/T	1.66604e-05	0.00288616	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712377	ATTTATATCGTTGAT[A/T]TCTGAATACTTGGGC	161436
rs775274469	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88707782	CACTAATTTAACTTC[A/G]CATAGTTCAGCCCAG	161436
rs775290582	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790618	GAGAAGACCTCAAAA[C/T]CCTTCACATTTACTC	161436
rs775319142	snp	C/T	1.65976e-05	0.00288072	splice-acceptor-variant	EML5	GRCh38.p7	14:88616880	TCATCTCCTAGAATA[C/T]TAGAGGGAAGGAACA	161436
rs775328427	in-del	-/TTTC			intron-variant	EML5	GRCh38.p7	14:88757777	TATACCATTTCTTTT[-/TTTC]TTTCTCTTTCTTTCC	161436
rs775339868	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692435	ACTTTTTTTCCTTGT[C/T]ATTATTCCCTAAACA	161436
rs775343289	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88632063	TAAATTTCACTCCTT[A/G]TATCTGTGGATAATT	161436
rs775352465	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88681490	ATGGGCTCAGTTCTA[C/T]TTACAATATCCTTCC	161436
rs775359142	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88654970	GCTCCTGTATTGGGT[A/G]CATATATATTTAGGA	161436
rs775360377	snp	C/G	1.65946e-05	0.00288046	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740523	AGGTCACCCGTCTTA[C/G]CAAAGACACCTCGTT	161436
rs775363802	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88716735	CCACTGCTCACCAAC[-/AC]ACACACACACACACA	161436
rs775368618	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764397	TCAGTTGTCAAATGT[A/G]TAAGTTGTTTATAGT	161436
rs775389719	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721560	GGGAAAACTGGCCAG[C/T]TATATGCGGAAAACT	161436
rs775404310	snp	G/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88793210	GGAAGCACCTGCCGG[G/T]TCCGCACGGTCCCTG	161436
rs775410796	snp	G/T	5.371e-05	0.0051819	intron-variant	EML5	GRCh38.p7	14:88627833	AGCTAAATAAAGATA[G/T]TATCAAAAAGTTGTA	161436
rs775423158	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88670309	TGGGTGATAGAGCAG[C/G]ACTCCATCTCAAAAA	161436
rs775430025	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88623809	GGCTTCTAGTGAGTG[A/G]GGGTGTGCAGGAGTA	161436
rs775457394	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88789989	TTTTCACTATGCATC[A/T]CATTTGTGAATATTA	161436
rs775485192	snp	C/T	1.73939e-05	0.00294901	intron-variant	EML5	GRCh38.p7	14:88625175	CATCAAAAGTTCAAA[C/T]AGAGTTTAAATAGAT	161436
rs775486795	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750580	CATAACCTTAATTAG[C/T]TTTAAGAACCTACGC	161436
rs775495865	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88758396	GACGAGGTTTCACCA[G/T]GTTGACCAGGATGGT	161436
rs775527668	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88645870	CCTCTTCTCTGTTCA[A/G]GATCTATTTATAATG	161436
rs775534291	snp	C/T	1.6577e-05	0.00287893	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658352	TTGTGACATGTGTAC[C/T]ATGGGCCACATACCT	161436
rs775540205	snp	C/T	6.61354e-05	0.00575007	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657382	AATTATTACCTTTCA[C/T]CAATTGAGGGTTCTT	161436
rs775542588	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88759956	TTGAATTTCCCTGAT[A/G]ACTACTCACATGGAC	161436
rs775554543	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88713354	TAAGAACATGCCACT[-/A]ACACTCCAACCTGGG	161436
rs775575200	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88724261	GCCTTGTGACAGAGC[A/C]AGACTCCATATCAAA	161436
rs775589096	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88672679	GAGAAGAATCAAATC[A/G]ACACAATAAAAAATG	161436
rs775589897	snp	A/C/G	6.46271e-05	0.00568419	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88687325	TCCTCCAGTTACAAA[A/C/G]CCCTATGGAAAAAAA	161436
rs775639305	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88665140	AAGTCACACAGAAAA[C/T]TTAGTAACAGAATTG	161436
rs775664803	snp	A/C	3.95296e-05	0.00444559	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715190	TGTACAACTTCCGTC[A/C]TATCTCTGTTAAAAA	161436
rs775669628	snp	C/T	1.68912e-05	0.00290608	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706277	GGGGTGCTATGTGAA[C/T]AGCATCTTTCAGTTT	161436
rs775669704	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88741270	CAAATCTAACATACT[A/C]TCTCTGATAGAAACA	161436
rs775722787	snp	A/T	1.67795e-05	0.00289646	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705586	GAGAGTCAGCCAGAC[A/T]TTCTGTAATTTTTAA	161436
rs775772040	snp	C/T	5.17603e-05	0.00508699	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642904	CTACCTGTAGCAACA[C/T]TGTGCAGAATTCCAA	161436
rs775787058	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647295	CTTGAACCCAGGAAA[C/T]GGAGGTTGCAGTGAG	161436
rs775788256	snp	C/G	1.74039e-05	0.00294985	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88754588	GATATGGTCTGCACA[C/G]TGTATGAATCCCAAA	161436
rs775790566	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88756442	CCACTAAGTAAAGGG[A/G]AAAAACAAGGATGTC	161436
rs775792013	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88699786	CAAGATTAACTTCCA[G/T]GCTTAGGCAACCAAG	161436
rs775809397	snp	A/G	2.09769e-05	0.00323852	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615834	CAGTGAGGTGTATGT[A/G]CACATTTCCAGACAA	161436
rs775809466	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783155	AGGTATGTTGCAGGG[A/G]CGGAGCCCTCATGGA	161436
rs775855167	snp	A/G	9.3835e-05	0.00684899	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694384	GGGTTCATCTTTACA[A/G]CAAAAATCTTATCTT	161436
rs775861572	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630671	CTCAGTTCGCAGTTT[A/G]CTTTGTGTCCTCACG	161436
rs775866403	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88689929	GTGCTTTGGAGAAAA[C/T]AGAAGCATAAAAAGG	161436
rs775890876	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88729148	TTCCAATCTGTGTGT[A/G]TGTACGTGTACATAT	161436
rs775924775	snp	C/G/T	0.000171625	0.00926202	intron-variant	EML5	GRCh38.p7	14:88736612	ATGCTGTAATAATGA[C/G/T]AGCAGCAGGAGGCAG	161436
rs775936225	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88741802	AGGCCCAAAGAAAAA[A/G]TTCAACTTTGTAATA	161436
rs775949824	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88727338	AGGAGCAGTGCAAAG[C/G]GATGTGAGTATACCA	161436
rs775982022	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88787336	AGGCAGGGATTCTTG[A/C]ACAAAACAGAAGCTC	161436
rs775995622	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88690654	CAAATTGATCAGCAA[A/C]TGGAGAATAAAGTTG	161436
rs776033708	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88676549	CACAGCCAAACTATA[C/T]CACTGCTCAAGGTAA	161436
rs776039311	snp	A/C/T			intron-variant	EML5	GRCh38.p7	14:88788201	AAAAAATCTATCTAC[A/C/T]GTGCAAATGTTATTC	161436
rs776056784	snp	C/G	1.84923e-05	0.00304069	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88663065	TGTTTTTTCCCTCTG[C/G]GAGCTTCAAAGAATA	161436
rs776056838	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88725474	AGTTAGAATTAGTGA[A/G]TAAGTTCTGAACATA	161436
rs776065027	snp	C/T	3.31367e-05	0.00407029	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626906	TCAGTAGCCCTTTTT[C/T]GCTAAGAAGAGCTCT	161436
rs776091533	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88762948	AGGCAGAAATACGTT[A/C]TTTGAAACCAATGAG	161436
rs776098718	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88660984	TAATTGGTTAAAACA[A/G]CTTCAAGTTTGAAGC	161436
rs776099311	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88654742	GATGTGGTGCTGAGA[A/C]GAATGTATATTCTGT	161436
rs776102903	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88637043	CTATATGATTTTTAA[C/T]AGAAGGAACAATAAA	161436
rs776109178	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88788447	TATTATTTTAACCTG[C/G]AACCATATAGTGTGG	161436
rs776113932	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88688488	CCTAGTTCACAAAAA[A/G]TATTATGAAAGTACC	161436
rs776125031	snp	C/T	0.000136156	0.00824982	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88618743	AAGAGTGGGGCCCAG[C/T]GTTAGGTCATAAAAA	161436
rs776153780	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88689313	CTTGCCAAACTGTTT[C/T]CCGAAGTTTATATAC	161436
rs776159649	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88639932	ATTCATCTGGTAGTA[C/G]TAACAGTGAAGAGAC	161436
rs776164682	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88790303	TTATACATTAAAGAT[A/G]TGTCATTTGGATAAA	161436
rs776174547	snp	A/G	2.12177e-05	0.00325705	intron-variant	EML5	GRCh38.p7	14:88618610	CGAAATGTAAAAGCA[A/G]AAGAACTTGCCACCT	161436
rs776174729	snp	A/C	1.6585e-05	0.00287962	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88643006	CGATAACCAAAAATG[A/C]GCTCCAACACAAGGT	161436
rs776177857	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88778237	GGAAAAAAAAGACAA[C/T]GAAACAACAAGAAAA	161436
rs776185222	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88712077	TGAATTCAAAAAGAA[C/T]TTTCTAATAAAACTT	161436
rs776202735	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88779948	TCTCTCATGTTTCTG[-/A]AAAAAAAATTTTTTT	161436
rs776203738	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617126	TAAAGTAGTACTTTA[C/T]GAAAACTGATAGAAC	161436
rs776228788	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88656990	ATCAATAGGGTTTTG[C/T]TTTTGTGGGTATTTT	161436
rs776235234	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88727548	TTGGGATTACAGGCA[C/T]GCACCACCACGCCTG	161436
rs776236451	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88707465	TCTCTATCTCCTCCT[C/T]CTGGTATGTGGCATT	161436
rs776244158	snp	C/T	1.99027e-05	0.00315451	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702568	CACCCACTGCTGCCA[C/T]ATGGTACACAATTTC	161436
rs776286096	snp	C/T	0.000276791	0.0117609	intron-variant	EML5	GRCh38.p7	14:88662993	TCTAGCCACTTTTAT[C/T]CACATGAACAACACT	161436
rs776297560	snp	C/T	6.31393e-05	0.00561833	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715173	CCTTCCTATCTTTAA[C/T]ATGTACAACTTCCGT	161436
rs776301608	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88691099	TGGCAACTGCTGGGT[A/G]TCTGGCAGTGGAATC	161436
rs776305968	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638688	TGGGTAGGGCTTTAT[A/G]TATACATAGATTTTG	161436
rs776314489	snp	A/G	1.76449e-05	0.00297021	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642897	GGGTTTCCTACCTGT[A/G]GCAACATTGTGCAGA	161436
rs776341469	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88789309	ACAAAAAAGTGACCC[C/T]AAAAGCCCTATATTA	161436
rs776342392	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88759799	GTTAGAGAAAAAGGA[C/T]AGGGTGGGTCCGTGT	161436
rs776355955	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88692364	CCTGGGCAACAGAGC[A/G]AGACTCTGTTTCAAA	161436
rs776360389	snp	C/T	1.6563e-05	0.00287771	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626940	TGCCAGGGTCCAGAA[C/T]TTCACATGTTTTACT	161436
rs776374644	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88750366	ATATGGTTAATGTTA[C/T]TTAATGTTTGCTTCA	161436
rs776375489	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88685228	TTAAGCTATTTTGAC[A/G]GTGAAAATCACATTA	161436
rs776413793	snp	C/T	1.69931e-05	0.00291483	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740404	CATGGGCTCCTTGTA[C/T]TGTTCGTATAAGATT	161436
rs776427348	in-del	-/TG			utr-variant-3-prime, downstream-variant-500B	ZC3H14, EML5	GRCh38.p7	14:88614103	GAAATATAATTTCTC[-/TG]TAGCCAAAAGCTGGC	161436
rs776427954	snp	A/C/T	0.000116039	0.00761629	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658249	CTTTTTTCTCGATAG[A/C/T]CTTCCATCTCATTTG	161436
rs776428804	snp	C/T	1.69295e-05	0.00290937	intron-variant	EML5	GRCh38.p7	14:88658152	TGTGCTAAATTTTCC[C/T]TATATTTTTGTTCAA	161436
rs776430545	in-del	-/TTG	1.95223e-05	0.00312422	intron-variant	EML5	GRCh38.p7	14:88627608	ACTACCTTTGTATTC[-/TTG]TTTTTTTAAAAATCA	161436
rs776439948	snp	A/T	1.86614e-05	0.00305456	intron-variant	EML5	GRCh38.p7	14:88712251	AGAGAGGTTACTTAA[A/T]ATTTTGAAAGAAAAG	161436
rs776449831	snp	C/T	2.32664e-05	0.00341067	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618723	TTGCAGTAGCTGATT[C/T]TGTTAAGAGTGGGGC	161436
rs776465663	snp	C/T	1.70353e-05	0.00291846	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622583	TTCTGCTGCACTGTA[C/T]CAGCTCATGGAACAT	161436
rs776473524	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88705917	ATACTATATGCAACA[A/G]ATGAATTGACATTAG	161436
rs776482937	snp	C/T	1.65734e-05	0.00287862	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88685033	AACCAGAAGTGTTAT[C/T]GGGCCACTTTTATCC	161436
rs776496186	snp	C/T	1.66776e-05	0.00288765	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715047	GGGATCCCAAACACT[C/T]GCCAACTTTTTTATA	161436
rs776513191	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88774827	GATAACATTCAAATC[C/T]ATACCAGCTCAGATT	161436
rs776514516	snp	C/T	1.70295e-05	0.00291796	intron-variant	EML5	GRCh38.p7	14:88646897	GCTAAATATGGAAGA[C/T]GACAAAAATACAAAG	161436
rs776522067	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88741563	GAGTTGGGGGGAAGT[A/G]GACACAGTGGCAAAC	161436
rs776522717	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88683226	AACCGTAGGCCAGCT[A/T]GTTTGTCCAAGAGAA	161436
rs776553960	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88629120	GATCACTCTATACAT[G/T]TTGCCAGTGATAAAT	161436
rs776563670	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88653781	TTGTGTCTCTGCCAG[A/G]TTTTGGTATCAAGAT	161436
rs776575269	snp	C/T	1.65619e-05	0.00287762	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88736440	CCCAAAGTTCACCTT[C/T]ACAATGCCCTTGCAT	161436
rs776584962	snp	A/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88793061	GGAGTTCGCGGGGCC[A/G]CGGTCTAGTTGCGGA	161436
rs776606973	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88769803	TCCGAAACCACAGGG[C/G]TCATTTAAGACTTCT	161436
rs776607370	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88783097	AAAAAAAAGAAAAAA[A/G]AAGAAGAAAGAAAGA	161436
rs776612821	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88730468	TTGCAGCAGCTTAAG[A/C]AATATGTCCAGAGAA	161436
rs776620036	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88671500	AACTACATTAAGTGT[G/T]CAACATAACCAGCTA	161436
rs776624852	snp	A/G	5.0583e-05	0.00502881	intron-variant	EML5	GRCh38.p7	14:88685163	ATGTTAAATGAAGAT[A/G]TTCTTTTAGACATAC	161436
rs776644838	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762705	CAAATCAACAGAATA[C/T]ACACTCTTCTTAGCA	161436
rs776652203	snp	A/C	1.66048e-05	0.00288134	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616281	TCAGGGCATTTGGTG[A/C]ACACAGAAGTCAAAG	161436
rs776663390	snp	C/T	1.65644e-05	0.00287783	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88621202	TTGCTAGTCCCCAGA[C/T]TGGCCCATCCACATG	161436
rs776669564	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88661408	GCCAAGATGTTTCTT[A/G]TAAAAGGGATATTCA	161436
rs776689710	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88736705	TTAAAGCCTGAAAGC[C/G]AAGCTACAAGTCTCA	161436
rs776712554	snp	A/G	1.66208e-05	0.00288273	intron-variant	EML5	GRCh38.p7	14:88665502	CACCTGAAAGAGAAA[A/G]AGCATATTAGGCAAT	161436
rs776715318	snp	A/T	1.65842e-05	0.00287955	stop-gained, nc-transcript-variant	EML5	GRCh38.p7	14:88681947	AGAGATCCCATATTC[A/T]TAAGGTTTTATCATC	161436
rs776719641	snp	C/T	1.69934e-05	0.00291486	intron-variant	EML5	GRCh38.p7	14:88736603	TAATATATAATGCTG[C/T]AATAATGATAGCAGC	161436
rs776731160	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88770918	TTAAAGTTCTTCTTC[C/T]TATTAATATTGCTGA	161436
rs776733425	in-del	-/CCA			intron-variant	EML5	GRCh38.p7	14:88677190	GATTACAGGAATGAG[-/CCA]CCACACCTGGCCAGA	161436
rs776742927	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88763933	TCCTAGTTTGCTAAG[A/C]ATTTTAAAAATATGA	161436
rs776804903	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88723199	AGGAGGATTGCTTGA[C/G]GCCAGGAGTTTGAGA	161436
rs776806284	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88652397	TCTCAGTTCTCCCTT[-/C]CCCATTACTAACGTG	161436
rs776854574	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711185	GGGTACTTTAATTGT[C/T]AGATATTTAGCCAGT	161436
rs776858214	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612728	CAGAGATCAGATCAG[A/G]TAGGTAAACTGCAAG	161436
rs776883239	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88624060	TCTTAGTCAACTATA[-/T]GTCACATTTTTTTTT	161436
rs776883953	snp	A/G	1.69312e-05	0.00290952	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88696874	CGGCACTAACACCAT[A/G]CTGGTGGTGGCCCTT	161436
rs776887498	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88764265	GCCAGCCTCATAAAC[A/G]CAGTTGAGAAGTAGT	161436
rs776910548	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767862	AGTACAATATCATTA[C/T]CTAAACTAAAAACCT	161436
rs776914960	snp	C/T	1.67497e-05	0.00289389	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661761	CTGTAACTTCTCCAA[C/T]TACTGGCCAAATTCC	161436
rs776920904	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756225	AATCAACAAATATGG[C/T]ATATTAACAGAAGAA	161436
rs776923929	in-del	-/TA	2.44257e-05	0.0034946	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615889	TTGCAGGGAGTTAAT[-/TA]TGTTTTTAGATTTTC	161436
rs776946710	snp	A/G	2.15603e-05	0.00328324	intron-variant	EML5	GRCh38.p7	14:88620975	GGAAACATTAAGTGA[A/G]GTACTTCTAAATTAT	161436
rs776959163	snp	G/T	3.46927e-05	0.00416475	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665384	TTTCTGTGATGAAAA[G/T]ACACAAGATCCTCTA	161436
rs776979151	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88711768	TGGCCAACATGGTGA[A/C]ACCCTGTCTCTACTA	161436
rs776986872	snp	C/T	1.70116e-05	0.00291642	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706269	CTCACCTTGGGGTGC[C/T]ATGTGAACAGCATCT	161436
rs776998995	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780864	AAGTGTGAGCCACTG[C/T]ACCTGGCTGAGTGGG	161436
rs777002866	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88703102	CTTTTATGAACTGCT[C/T]GGACTGCAAATAGCT	161436
rs777039153	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88660672	AGCTTGAACCCGGGA[G/T]GTGGAGGTTGCAGTG	161436
rs777055920	snp	G/T			synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688334	TGTTTTTACAAGAAA[G/T]ATGTCTCTCCAGATA	161436
rs777057960	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88704320	CCCTTTGCCTTCTGC[C/T]ATGAGTAAAAGCTTC	161436
rs777065655	in-del	-/ACTG	2.26165e-05	0.0033627	intron-variant	EML5	GRCh38.p7	14:88695481	TAATGAGAGAGATAA[-/ACTG]ACTATTAACATTCAG	161436
rs777070794	in-del	-/TAGGTAC	3.4747e-05	0.00416801	intron-variant	EML5	GRCh38.p7	14:88714901	CTCTAAAATATTGTA[-/TAGGTAC]TACAAATCTATAATT	161436
rs777101352	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88751533	TTTGTTGGTTTTTTT[G/T]TGATAGTGTTCGAAT	161436
rs777111206	snp	C/T	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688322	ATGCGCTTTCACTGT[C/T]TTTACAAGAAAGATG	161436
rs777156507	snp	A/C	6.79521e-05	0.0058285	intron-variant	EML5	GRCh38.p7	14:88736604	AATATATAATGCTGT[A/C]ATAATGATAGCAGCA	161436
rs777167626	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88740694	TAAGAAATTGCCTTA[C/T]GATAAAATAGCATTC	161436
rs777179526	snp	C/T	2.13145e-05	0.00326447	intron-variant	EML5	GRCh38.p7	14:88618600	TTCACTAACACGAAA[C/T]GTAAAAGCAGAAGAA	161436
rs777197204	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88631272	AGGCTGGAGTGCCAT[A/G]ATGTGATCATGACAC	161436
rs777208321	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88635660	AGAGTTTGGGCAGCA[C/T]GAGACAACCTGTCTC	161436
rs777209271	snp	C/T	9.33228e-05	0.00683028	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88694337	ATTTCATGTGTTTAA[C/T]TCCAGCTGTAATTAG	161436
rs777213861	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88770728	TTTCATCCACATAAT[A/G]CCTAGTATATTGCTG	161436
rs777223943	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88663327	TTTGATTTTTGTATA[C/T]GTATATACATAAAAA	161436
rs777224918	snp	C/T	8.62478e-05	0.00656631	intron-variant	EML5	GRCh38.p7	14:88657340	TTTTTAATGACAATA[C/T]CTTTTTCTTCATCTA	161436
rs777234270	snp	C/G	1.65949e-05	0.00288048	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88626865	AATAGCGAGCATGGT[C/G]TGCATCCGGGCATCT	161436
rs777239208	snp	C/G	0.000979432	0.0221078	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705579	TCACTATGAGAGTCA[C/G]CCAGACTTTCTGTAA	161436
rs777257532	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88674257	CTGGGCTAAAAGGGT[A/G]AGACTTCATCTCAAA	161436
rs777265157	snp	A/G	1.66593e-05	0.00288607	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618291	AGATGTTTTCCTGAA[A/G]GCACTTCATAGACAT	161436
rs777267338	snp	A/G	3.40692e-05	0.00412716	intron-variant	EML5	GRCh38.p7	14:88625165	GAGACAAACTCATCA[A/G]AAGTTCAAATAGAGT	161436
rs777283646	snp	A/G	1.6588e-05	0.00287988	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625051	CCGTTGTGAGCTCTC[A/G]CCACGATTCTACACA	161436
rs777304248	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88787084	ATATTCTCTCATAAC[A/G]CAAAACCACTGCACA	161436
rs777304393	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88635736	TGGTGCTATGAACTG[G/T]ATGTCTGTCTTCCCC	161436
rs777318069	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88616978	TCTAAGTACCCTATC[A/C]TGTTACTTAAAATAC	161436
rs777336067	snp	A/T	3.60094e-05	0.00424304	intron-variant	EML5	GRCh38.p7	14:88739055	ACGACAAATATTTTT[A/T]AAGAACATCTACTAT	161436
rs777359580	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88782896	ATCAGCCGGGCCAAC[A/G]TGGTGAAATTCTGTC	161436
rs777363432	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88665721	GGGCGAGGGGGAAGA[C/G]AGAAGAGGGAAGGGA	161436
rs777367934	snp	C/T	1.66799e-05	0.00288785	intron-variant	EML5	GRCh38.p7	14:88746303	TTTATGTCCAAGAAG[C/T]CCAGGAAGGAATAAA	161436
rs777368846	snp	C/T	1.71302e-05	0.00292657	intron-variant	EML5	GRCh38.p7	14:88704846	CAAATAAATGAAAGA[C/T]AGTTGTTTTATACCC	161436
rs777382776	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88760876	ATAGACCTTGCATAG[A/G]TTTTGTAAAATTTAT	161436
rs777401777	snp	C/T	1.94729e-05	0.00312027	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706388	ATCTGACATTAGTTA[C/T]GTGAGCTGAATGGCC	161436
rs777436070	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88758304	TTCAAGCAATTCTCC[C/T]GCCTCAGTCTCCCAA	161436
rs777460643	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711600	ACTTCTCACCAGGTT[C/T]CTCCCTTAACACCTG	161436
rs777472845	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88782022	GAAAATGTGGGAAAG[-/T]TTGGAACTTCCTAAA	161436
rs777476372	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88621986	TACTATTCCTATCTG[C/G]CTGTGTAAACTTGTA	161436
rs777476577	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88775768	TTGAGCAAACATAGG[C/T]AGTAACCAGGGACTG	161436
rs777484973	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88749028	TGAAGAAATAATAGT[-/AA]AAAGTTTCCTAAATT	161436
rs777490337	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88783699	GAGAGAGAGACAGGC[C/T]CCAATATAATAGCTG	161436
rs777495243	snp	C/T	1.70278e-05	0.00291781	intron-variant	EML5	GRCh38.p7	14:88643065	ATTCTTCCTCATGTA[C/T]AAATGTTCACCACTG	161436
rs777500376	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88692731	TGTTTAAGCATGTGG[A/C]AACAAAATTACAAAT	161436
rs777512170	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88633238	ATTGTTTTTAACACA[C/T]TTCTTGCCATCTCAT	161436
rs777514023	snp	C/G	1.67539e-05	0.00289425	intron-variant	EML5	GRCh38.p7	14:88625136	AGTTATTCTGAAAAG[C/G]AGTGGGGGAGGGGGA	161436
rs777548159	snp	C/T	8.35471e-05	0.00646271	intron-variant	EML5	GRCh38.p7	14:88664657	TTGCTTGACATTTTC[C/T]ATCTTTGGAAATACT	161436
rs777569937	snp	A/C	2.4033e-05	0.0034664	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657466	GCTCTGATGGTGTAA[A/C]TGATTTCATTCTCCC	161436
rs777598923	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777224	ACACAACGGAGCTCC[A/G]ATACATCTGGCAGAA	161436
rs777600955	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88763951	TTTAAAAATATGAAT[A/T]AGTATTAAATTCTGT	161436
rs777604466	in-del	-/CT			intron-variant	EML5	GRCh38.p7	14:88760480	ACCATATCTATATTA[-/CT]TTTCCACAAATTGCA	161436
rs777610591	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88707091	GATGTGTTTTGGGTA[A/C]GGGCAATGTTGTATC	161436
rs777610733	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88721347	AGGCAGGAAGCATCA[C/T]GCTACTGAACCTCAA	161436
rs777644272	snp	A/G	1.66081e-05	0.00288163	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714973	TCTTTTCCCATTTCC[A/G]TCATTTGTCTGCAAA	161436
rs777651313	in-del	-/A	0.00784126	0.062122	intron-variant	EML5	GRCh38.p7	14:88687334	TACAAACCCCTATGG[-/A]AAAAAAAAGGTTCAA	161436
rs777654067	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88765290	TTCTAGAGTCTCTGG[A/G]GATGAGTCAGCTTCC	161436
rs777707571	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88696166	AGCAACTCTTTGAAT[-/AT]ATATATATATATATA	161436
rs777743661	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88726206	CTCAGCTTGTTAAAC[A/G]GAGAGGGATCATTAC	161436
rs777744952	snp	A/G	1.65809e-05	0.00287926	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88642978	GTGAACATTATTCCT[A/G]CAGTCTCTGCCTCGA	161436
rs777746206	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88699341	GAGATAAAAAGGGGA[C/G]TTGGAGAGTCAGACT	161436
rs777773548	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88725908	AGAGAGAACTGTGTT[-/A]ATAGTTTCTGAATTG	161436
rs777783714	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88706483	AACAAAATACCATTT[C/T]AAACAATTTTTATAT	161436
rs777819765	in-del	-/TCTA			intron-variant	EML5	GRCh38.p7	14:88699275	ACGTGTTGGACAAAT[-/TCTA]TCTATCTCAGAAGGC	161436
rs777841909	snp	G/T	3.22575e-05	0.00401593	intron-variant	EML5	GRCh38.p7	14:88726514	CTGAAGATAAAATTA[G/T]TATGTGTTTCTACCC	161436
rs777845195	snp	A/G	1.71255e-05	0.00292617	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696863	TGAGAAATCAACGGC[A/G]CTAACACCATACTGG	161436
rs777862683	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88704257	ACCCCCTTCCCTTTC[A/G]ATCCCTTTTTCCTTG	161436
rs777864081	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88645364	CGTGTCATAATGTAA[A/G]TAACAGCACAAGAGT	161436
rs777881357	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88653680	AAGCTTTTTGATGTG[C/T]TGCTGGATTTAGTTT	161436
rs777887130	snp	A/T	3.31406e-05	0.00407053	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658315	GTAACCAACATGCTG[A/T]CATCATAAGTCCAGC	161436
rs777894753	snp	A/G	1.67329e-05	0.00289243	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88754535	CTAAGTCAAACGCCA[A/G]GCAAGCTATACCATG	161436
rs777899033	snp	C/T	5.80063e-05	0.00538515	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715163	TGAATTGCCTCCTTC[C/T]TATCTTTAATATGTA	161436
rs777899546	in-del	-/GAGT			intron-variant	EML5	GRCh38.p7	14:88741145	TCCAGCCTGGGCGCA[-/GAGT]GAGACTCCGTCTCAA	161436
rs777908521	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88724927	AATTATAACAGTATG[A/G]ATAGCCCAACAGGGA	161436
rs777916141	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88705103	GTAGTCTTAAATGAA[A/C]AGTTAATTCATGAAA	161436
rs777935882	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613868	TCTATATGGCCTATC[A/G]TGTTTCTTCACCTTC	161436
rs777948246	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88786983	GGTCACTGGTAACCT[C/G]AACAAGAACTGCTAT	161436
rs777961460	snp	A/G	5.55756e-05	0.00527112	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88744056	ACAGCTGACAAGTTT[A/G]TTTGGCTGGTACAAA	161436
rs777973257	snp	C/T	0.000103923	0.00720769	intron-variant	EML5	GRCh38.p7	14:88634520	ATTATCTATAAATAA[C/T]ATAAATCTGTAAAAT	161436
rs777987436	in-del	-/G	1.65968e-05	0.00288065	frameshift-variant, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625010	TAAGTCCATCTCGCA[-/G]GGTGGTGTACATGGC	161436
rs777987512	snp	A/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88746207	GTATGACCAGGAGCC[A/T]TAGACAACATTTTTC	161436
rs777988179	in-del	-/AG	1.69989e-05	0.00291533	intron-variant	EML5	GRCh38.p7	14:88646935	TTGTAAACACAGCAA[-/AG]AGAGGATTACCTGGA	161436
rs777993722	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88636505	GTCTCTACTAAAAAT[A/T]CAAAAATTAGCCAGG	161436
rs778006424	snp	A/C	1.73999e-05	0.00294952	intron-variant	EML5	GRCh38.p7	14:88740591	AAAGGTATATAGTAT[A/C]ATCAAATTACCAAAG	161436
rs778034101	snp	A/C	3.55771e-05	0.0042175	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661680	ATCTAAATAACTTCA[A/C]AAATCCCAAATCGTC	161436
rs778039798	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88643303	TAGTTCTTAAGATTT[C/T]ACATGTAAACACTGA	161436
rs778046635	snp	A/G	2.37544e-05	0.00344625	intron-variant	EML5	GRCh38.p7	14:88712494	TCCTCCTAAAAATAA[A/G]TCAGAGTCTTAATTT	161436
rs778049813	snp	C/G			upstream-variant-2KB	EML5	GRCh38.p7	14:88794503	CTAAGGCCCATGTAG[C/G]GTACCCTGGGCAAAA	161436
rs778062425	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88780297	TATTGACTGTCTTTG[C/T]TCTAGGCTATTTTTT	161436
rs778074845	snp	A/C	0.000155748	0.00882324	utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615804	GTTAATTTCTGTAGT[A/C]ATCTCAGCATCTCTC	161436
rs778081830	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88656010	AGCAATGCTTTTACA[A/C]TGTTGGTGGGAGTGT	161436
rs778097212	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88703590	ATTTTAACACTAGAG[-/A]AAAAAATACTTGTAC	161436
rs778117682	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767693	AGCAAAAGATTTTAA[C/T]TTTTTTAAGAAGTGT	161436
rs778148260	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88668226	GCCTTGTAGTCTCAT[C/T]TTCTGACTGGACAGT	161436
rs778151289	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88785900	ATGTCACTATTTTGA[A/T]TAAATAGTTCCAATA	161436
rs778152551	snp	C/T	5.48561e-05	0.00523689	intron-variant	EML5	GRCh38.p7	14:88638911	AACTCTGAGAACCTA[C/T]AAAAAAGAATTTGAG	161436
rs778162497	snp	A/G	1.91316e-05	0.0030928	intron-variant	EML5	GRCh38.p7	14:88702405	TTAAACTCAAACAAA[A/G]GTGTAGCTTATCTGG	161436
rs778182745	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88672001	GATCATAAAGACAGA[A/T]AATTAACAAAGATAT	161436
rs778188724	snp	A/G	1.65811e-05	0.00287929	intron-variant	EML5	GRCh38.p7	14:88621316	CCTGAAACACAAGCA[A/G]GACCAATACAGTGAA	161436
rs778195698	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88641191	GACATACAAAGAAAA[G/T]CTGGTGCCAATCCTA	161436
rs778218187	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88643093	CTGTTTTGTTGTATA[C/T]GTAATACTAGTAGTG	161436
rs778221718	snp	A/G	1.65616e-05	0.00287759	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88688292	CAATGCATGCATACT[A/G]AACACTGGCCCATCA	161436
rs778227302	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88781019	AAGATGACACAGAAA[A/C]CTAACCATCACAAGC	161436
rs778246373	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88763800	TGACAAGAATAGACA[C/T]TCTGGTCTTTTTCCT	161436
rs778276469	snp	C/T	1.65723e-05	0.00287852	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621173	AGAAAGGAAAAAATC[C/T]CTGGAAGGATGTGTT	161436
rs778277049	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88662784	TCCTGAGCACAAGCA[A/G]TCTGCCTGCCTCTGC	161436
rs778281977	snp	C/T			utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88615659	TGCATATAGCAAATA[C/T]TTTGAACAGATCAGT	161436
rs778292654	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88716992	GTTTCTTTTAAGAAG[A/C]AGAAGGAGGCAAAAG	161436
rs778301510	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88750033	ATTCCTTCGTGCATT[A/G]TCTATGACTGCTTTC	161436
rs778322149	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88645274	CAAGTGATCCGCCTA[C/T]CTCGGCCTCCCAAAG	161436
rs778325916	snp	C/T	1.66485e-05	0.00288513	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625116	GATGGTACCTGTAAA[C/T]GTCAAGTTATTCTGA	161436
rs778338779	in-del	-/TTGTT			intron-variant	EML5	GRCh38.p7	14:88662337	GCAACACAATTTTTC[-/TTGTT]TTTTTTTTTTTTTTT	161436
rs778339335	snp	C/T	1.68684e-05	0.00290412	intron-variant	EML5	GRCh38.p7	14:88684966	TCTTATATATTGAAA[C/T]AATCAATTGTATGTA	161436
rs778339349	snp	A/G	0.000115267	0.0075908	intron-variant	EML5	GRCh38.p7	14:88649933	ACTCCCTGCCTTCAA[A/G]AGGAGCAAGGGGGAA	161436
rs778351620	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88740835	TTTAAAATATGCTAT[G/T]CTTTCCTTAGGTTTC	161436
rs778358639	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88781635	CTGGACAAGGTAACT[A/G]AATCATGGTGACGAT	161436
rs778367224	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88682631	CTCCCCCCAGCTCGC[A/G]GTCAGAGCACTATCT	161436
rs778385503	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88688095	CACTGCAGACCTATT[C/T]CATTCTGTGTTCGGG	161436
rs778388973	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88630100	CAATGGCATGATCTC[A/G]GCTCACTGCAACCTC	161436
rs778390734	snp	C/T	5.12869e-05	0.00506368	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88681891	TGAGAGCCTCTTACC[C/T]TTTTTCAGCTTCCGG	161436
rs778393244	in-del	-/ATTT			intron-variant	EML5	GRCh38.p7	14:88633219	TATTGCCATCATCTC[-/ATTT]ATTGTTTTTAACACA	161436
rs778398858	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88738416	TTTTAATCCCCAAGA[-/G]GAAAAAAAAAAAATC	161436
rs778419508	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88712636	AGATAAGTTTGGGTT[A/G]AGAGAAAAGAAAACT	161436
rs778423580	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88697796	GCTGGAGTGCAATGG[C/T]GCTATCTCGGCTCAC	161436
rs778433263	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88682582	TCTGGTTGGAAACTC[C/T]GAGACTGATGCAACC	161436
rs778476998	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88699084	ATTAAAGTACACTTA[A/G]GGCATCTCACTCAGG	161436
rs778510235	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88772107	TAGTAAATGATATCA[-/C]CATCCATTCAATTGC	161436
rs778523979	snp	A/G	3.42472e-05	0.00413792	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88705548	TGGAACATCAGACAG[A/G]TCTGAATCTGATTCA	161436
rs778531126	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88690330	TGACTTCTGGATTGA[A/G]AATAGATACAAGGGA	161436
rs778532595	snp	C/T	1.96203e-05	0.00313206	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715118	CATCCAACAGCAAGG[C/T]AAGTTCCATCTGGTG	161436
rs778556437	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88630177	CTGGGATTACAGGCA[C/T]CTGCCACCATGCCTA	161436
rs778556796	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88780809	CGATCTCTTGACCTC[A/G]TGATCCATCTGCCTT	161436
rs778603557	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612936	GATTAATGCAAAAGG[-/T]GGTAATAAAGACTGC	161436
rs778606675	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88782731	TTGGTCCTGCAAATG[C/T]GCAGAAGACAAGAAC	161436
rs778613843	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88786852	TCTTTTTCCTCCCAG[A/T]CTCAGGTATCTCTTT	161436
rs778618518	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88619954	ACAGGCATGAGCCAC[C/T]GCGCCCGGCCTGAAG	161436
rs778623099	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88751160	CCTATGCATAGATTA[C/T]GCAACAACAGACAGG	161436
rs778632647	snp	A/G	1.75029e-05	0.00295823	intron-variant	EML5	GRCh38.p7	14:88664468	ATGAAACTTTTATCA[A/G]GTATTAAGTTATTTA	161436
rs778647306	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88646724	AACTTATAAAATTAT[A/T]CAAGTTGAATGGATA	161436
rs778678989	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88651818	TTAAGTATTTACCAG[A/G]TATCTCCTCAGTTAA	161436
rs778725645	snp	C/T					GRCh38.p7	14:88714596	AAGTGGCAGATACAT[C/T]ATTTAGCTTGATTGT	161436
rs778738397	snp	A/T					GRCh38.p7	14:88774416	ATACATTGGAACGAA[A/T]CTTGAAAGAGGCTAG	161436
rs778758436	snp	C/T					GRCh38.p7	14:88736245	ACCTTGTGATCTGCC[C/T]GCCTTGGCCTCCCAA	161436
rs778760677	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717899	AAAATACAATGTAGT[A/G]TTATACTCCATACTA	161436
rs778764826	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88632282	CACCCTGCTTAACTG[-/T]TTTTTTGCTTGGACT	161436
rs778791805	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88775476	ATTGGCAGTAGTCTG[A/G]TAGTGCTCTCCATGG	161436
rs778817670	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88689434	CAACTGAATTTTATT[A/G]TAGTTTAAATTTGCA	161436
rs778832201	in-del	-/A	6.53275e-05	0.00571485	intron-variant	EML5	GRCh38.p7	14:88705442	GATAAAGAAGAAATT[-/A]AGACTTTTTAGAGAA	161436
rs778842649	snp	A/G	3.5979e-05	0.00424125	intron-variant	EML5	GRCh38.p7	14:88618373	AGAATTCCATTAGGT[A/G]AGAGACAAAATCCAC	161436
rs778878418	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88762466	AGTGAGCTGAGATCA[C/T]GCCATTGCACTCCAG	161436
rs778882591	snp	C/T	1.8542e-05	0.00304478	intron-variant	EML5	GRCh38.p7	14:88661850	AAATGAAAAACAATG[C/T]TGTAAGTTTGGATTA	161436
rs778883002	in-del	-/AGT	4.79283e-05	0.00489508	intron-variant	EML5	GRCh38.p7	14:88754694	ATAAGGAAATAAATA[-/AGT]AGTATTATTAAAAAT	161436
rs778887319	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88705748	ACAGATGTCAGTAAA[C/T]TGTACTACAGATTAT	161436
rs778900762	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88724495	AGGTGCTAAAATACA[G/T]TCTTATTAGGAATAA	161436
rs778911015	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88660640	CCCAGCTACTCAGGG[C/G]GCTGAGGCAGGAGAA	161436
rs778911919	snp	A/G	0.000346141	0.0131511	intron-variant	EML5	GRCh38.p7	14:88638956	ATTTTAAGATGTAAC[A/G]GCCAAAAGCACTTAC	161436
rs778933505	snp	A/G	0.000132485	0.00813788	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688416	TACACTGCACACATC[A/G]TTGTGTCATTTTTCC	161436
rs778935987	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88621824	ATATCTATAGGGCAT[A/G]GGGTAATACGCATAA	161436
rs778938754	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88666808	TGAAATCTGATGAGG[A/T]AAGGACAGGGTATAT	161436
rs778941879	in-del	-/TTTTC			intron-variant	EML5	GRCh38.p7	14:88780581	AAAAAATCTTTTTTT[-/TTTTC]TTTTAAGATGGAGTC	161436
rs778943250	in-del	-/CT	1.67705e-05	0.00289568	intron-variant	EML5	GRCh38.p7	14:88684986	ATTGTATGTAAAGAA[-/CT]AAAAAAACAAATTAG	161436
rs778944407	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690248	TACTTTTGCTTTACA[C/T]GAGATGCAAAACATT	161436
rs778947342	snp	C/G/T			intron-variant	EML5	GRCh38.p7	14:88716852	TGAATTATATGACCA[C/G/T]TCTCTCACATGAAGA	161436
rs778950020	snp	A/G	3.3644e-05	0.00410132	intron-variant	EML5	GRCh38.p7	14:88746136	CCTGAACTCTCTTCT[A/G]GTCTTTCCCTTCCAG	161436
rs779013162	snp	A/G	1.66532e-05	0.00288554	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712368	ATCTACTGAATTTAT[A/G]TCGTTGATATCTGAA	161436
rs779027002	snp	C/G	1.67055e-05	0.00289006	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685140	TATCTTCCAAGAGAA[C/G]ACCTGAAATGTTAAA	161436
rs779061795	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88704001	TAAGTCACCACTAGC[A/G]TTGCCTTATTCACTC	161436
rs779062599	snp	C/T	1.65677e-05	0.00287812	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740484	AATTCATCCCTTGCA[C/T]AGGCTAGGCACAGTA	161436
rs779070706	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88617574	AAGAGTTTGAGACCA[A/G]CCTGGGCAATATTGT	161436
rs779082814	in-del	-/G	0.000455996	0.0150927	intron-variant	EML5	GRCh38.p7	14:88649953	GCAAGGGGGAAAAAA[-/G]TAGGAAAACATATAA	161436
rs779082900	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88715497	GAAATAAAGTAATAG[A/C]TTTTTATGGTAAAAG	161436
rs779097491	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766642	ATCTCGCCCTGCCTC[C/T]ATTTGCCTTCTGATA	161436
rs779106735	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773029	CTAATTATTTCATGT[C/T]TCCCTTCATGCTTAC	161436
rs779121960	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702612	TAAAACAGATTACTT[C/T]GACAGTCATAACCTC	161436
rs779137419	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88745078	TTCCAAATAGTCATG[G/T]GCAAAATGCTTTGAT	161436
rs779160719	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88760746	TAAAAAACTTTGAAG[A/T]GAAGTGACATCTTAA	161436
rs779167818	snp	A/G/T	1.65602e-05	0.00287747	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687257	CTTTTTATAGCATAG[A/G/T]TCTTGAGACATCTTT	161436
rs779187803	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	ZC3H14	GRCh38.p7	14:88612295	GTTTGAAAAGCATGA[C/T]TATACAGGCCTCTCA	161436
rs779191653	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88767462	GCTAAGAGTCTAGGA[C/T]GTTAGCCTCTGCATA	161436
rs779193637	snp	C/G/T	3.34086e-05	0.00408698	intron-variant	EML5	GRCh38.p7	14:88616928	GCAAGTGCGGGCAGG[C/G/T]TGACTATATTCAAAA	161436
rs779206247	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88680615	CTGTACTCATTATAG[C/T]ACTAGCTTTCAAATT	161436
rs779212135	snp	A/C	1.65737e-05	0.00287864	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616823	ACACAGGCACAGTTG[A/C]CATCAGCTTTCTCAG	161436
rs779215547	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88791657	ATTTTAATGAAGATG[A/G]AGAGAACTGGAAATC	161436
rs779225126	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88773719	TGGTTTTATTTTGTT[G/T]GTTTTCTTTTAACTT	161436
rs779228207	snp	A/G	0.000113231	0.00752348	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88620890	TGTAACACACAGTAC[A/G]AGCAGCATGTCCCAA	161436
rs779229937	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88693089	GATACACTTTTGTAT[C/T]ATTTAATAGCATATG	161436
rs779242785	snp	A/C/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613763	TGAATGGAACAAAAG[A/C/G]TGCCAGAAGTCCCAG	161436
rs779264400	snp	A/C	4.20089e-05	0.00458287	intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88792266	TGCAAACTCCGGGAG[A/C]GGCTTGCAGGGTGAC	161436
rs779266911	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88778965	ATGAGTTAGGAGCCT[A/T]TGTGATGAAACTTCC	161436
rs779278041	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88617958	TGCCAGTCATTAAAT[C/T]TAGCATTAAGAAAAA	161436
rs779286353	snp	A/G	0.000109896	0.00741188	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792423	CGCAGTGTAGTAGAG[A/G]TTGTTGCGGCACTGG	161436
rs779298463	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88759422	TGTGTGGTGGCTTGT[A/G]TCTGTAAACCCAGTG	161436
rs779307940	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88641059	CAACCTCTCAAGATT[A/G]AATCAGGAAGAAACT	161436
rs779325229	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88655830	AACAGACACTTCTCA[A/G]AAGAAGATATTTATG	161436
rs779343953	snp	C/G	9.94975e-05	0.00705258	intron-variant	EML5	GRCh38.p7	14:88634445	ACAATATAAATAAAG[C/G]AGAAAATGTTTAGTT	161436
rs779363411	snp	G/T	1.65839e-05	0.00287953	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665447	TCGTTGAGACCTACG[G/T]CTAAAGCTTTACCAT	161436
rs779367460	snp	A/C	4.21638e-05	0.00459131	intron-variant	EML5	GRCh38.p7	14:88696970	AAAATAGAATTATAG[A/C]AGCTATTAAATACAA	161436
rs779391185	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88728692	AAATCCACCTATAAG[C/T]GGACCCATGCAGTTC	161436
rs779397404	snp	C/G	1.65627e-05	0.00287769	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627776	TAGGATAGATAAAGT[C/G]TGCTTGTTCATTGCA	161436
rs779402621	snp	C/T	6.6368e-05	0.00576017	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88621149	TCTCACTGTCCCATC[C/T]TCTGCAGCAGAAAGG	161436
rs779403508	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88723114	TATACTATTCATTCT[A/T]AAAAAGGAAGAAAAT	161436
rs779408125	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88674589	GTGAATTCGAGATGA[C/G]ATTTGGGTGGGGACA	161436
rs779417757	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88638972	GCCAAAAGCACTTAC[C/G]CAGAACAATAAACTA	161436
rs779422818	in-del	-/TTTATTTA			intron-variant	EML5	GRCh38.p7	14:88707271	ATAATAGGGATATAT[-/TTTATTTA]TTTATTTATTTATTT	161436
rs779442335	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88708717	CATCATTTAATAGCA[C/T]GGAAGTCTGAGCATT	161436
rs779445765	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88730552	TTGAGAATATTGGGA[A/G]CACTACCAATAATTA	161436
rs779449320	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710859	AAAATATTCACACAG[C/T]AGTTCAAAGAACTAC	161436
rs779469620	snp	C/T			upstream-variant-2KB	EML5	GRCh38.p7	14:88794728	TACATGTAAATTTTA[C/T]GAGACGAGATGGAAG	161436
rs779474720	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765551	ATTTGCTTTTAAGGG[C/T]TCACATAATTAGACT	161436
rs779518895	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88695938	CAATCATTCAAGCAA[C/T]ACATAATGAATATAT	161436
rs779522799	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88712721	CACATTGCCTTGAAT[C/G]ATTAGCTTAGCAGGT	161436
rs779527792	in-del	-/AACA			intron-variant	EML5	GRCh38.p7	14:88762801	AAGAATGGAAATCAT[-/AACA]AACAGTCTCTCAGAC	161436
rs779529782	snp	C/G			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88791860	GCCACCCTGGGCGCG[C/G]TCCCCGGGAGCAGCC	161436
rs779531126	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88660445	CATAGGTACGTAGAA[C/T]GCCAAAGAATCTGTT	161436
rs779540967	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88694900	AGTTCCTCCTTTAAA[G/T]CATTGTTAATATTAC	161436
rs779543531	snp	C/T	6.63394e-05	0.00575893	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88665445	CATCGTTGAGACCTA[C/T]GGCTAAAGCTTTACC	161436
rs779545463	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88777719	CAGTGGCTCATGCCT[A/G]TAATCCCGGCACTTT	161436
rs779558799	snp	G/T	3.53451e-05	0.00420372	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88696848	GCAAACAGCCTTACC[G/T]GAGAAATCAACGGCA	161436
rs779574333	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88724008	GGGCACAGTAGCTCA[C/T]GCCTGTAATCCCAGC	161436
rs779577889	in-del	-/GAT			intron-variant	EML5	GRCh38.p7	14:88633635	AAAGCAGTGCAAACA[-/GAT]GATGAGTGTCATCTA	161436
rs779582346	in-del	-/C			intron-variant	EML5	GRCh38.p7	14:88629315	TAAATAGCAAGTAAT[-/C]TTAAATTCAATGACT	161436
rs779582548	in-del	-/TCAAGATATATAG			intron-variant	EML5	GRCh38.p7	14:88685480	TAATTTTAATTCAAT[-/TCAAGATATATAG]TCAGCCCTCAGTATC	161436
rs779596460	snp	G/T	1.94551e-05	0.00311884	intron-variant	EML5	GRCh38.p7	14:88696829	GTTAATTCTTACTGA[G/T]ACAGCAAACAGCCTT	161436
rs779627808	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88711417	CAGGAAACTTACAAT[C/T]ATGGCAGAAGGTGAA	161436
rs779647080	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88619648	CTAACCTCCAGTTAT[G/T]AAGGTGAAATGACAC	161436
rs779662639	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88753117	AAGAATATTGTTTGT[A/G]ACACACACCCTCTGG	161436
rs779667500	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761298	TGGTGGTTTGCTGCA[C/T]TCATCAACCTGTCAT	161436
rs779668791	snp	C/T	3.38284e-05	0.00411255	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792381	CACCACGCCGACCCC[C/T]GCCACGAAGTATACG	161436
rs779722367	snp	C/T	6.31812e-05	0.0056202	intron-variant	EML5	GRCh38.p7	14:88754704	AAATAAGTAGTATTA[C/T]TAAAAATTGCTTATA	161436
rs779737810	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88629435	AATGGAATTGTCACA[C/T]ACTTAGACTGTTCTA	161436
rs779750595	in-del	-/TTC			intron-variant	EML5	GRCh38.p7	14:88697595	CAGGTAAACTATCAA[-/TTC]TTAATTATTCCTCTA	161436
rs779776748	snp	A/G	1.74093e-05	0.00295031	intron-variant	EML5	GRCh38.p7	14:88618350	TTTCATCAGATTAAA[A/G]TGGGACAAGAATTCC	161436
rs779784241	in-del	-/GCGGCGGCGACGG	0.000230867	0.0107415	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792539	CTCCCGCTCGGGCCC[-/GCGGCGGCGACGG]GAGGCGGCGGCGGCC	161436
rs779784500	snp	C/G/T	3.35871e-05	0.00409788	intron-variant	EML5	GRCh38.p7	14:88664671	CTATCTTTGGAAATA[C/G/T]TTTTTTACACTCTGC	161436
rs779792236	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88642408	TTGGATCAAACAAGG[C/T]ATCATCATAGAGCCA	161436
rs779805044	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88733567	GGCACTTGGTAATAG[C/T]AGTTCTACAATGAAA	161436
rs779808263	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88667880	CTCACAGTTCAATGA[C/T]TTTGCCCTAGGTTAA	161436
rs779830067	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88757790	TTTTTCTTTCTCTTT[A/C]TTTCCCTCTTTCCTT	161436
rs779838045	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88786671	AGTTTCCCCCACACT[C/G]TTCTCATGGTAGTAA	161436
rs779845224	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88748023	AGTCCTGTAATCACC[C/T]GAGCTTCCATCTAGG	161436
rs779870237	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88631640	CTGGGCGTGGTGGCA[C/G]TCGCCTGTAATCTCA	161436
rs779885081	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88782314	GAAGAAATTTCTAAG[C/T]GACAAAGAATTCAAG	161436
rs779903107	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88754781	AACATTAGACTTTAT[C/T]CACTTTAGACAATTT	161436
rs779906020	snp	A/G	3.31807e-05	0.00407299	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88625086	GTGATCTTTCCACAC[A/G]CAGACATCACCACTG	161436
rs779917123	snp	A/G	1.76949e-05	0.00297441	intron-variant	EML5	GRCh38.p7	14:88740603	TATAATCAAATTACC[A/G]AAGAATTCTTATAAA	161436
rs779935749	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88650371	AGGCAGGAGAATCAT[G/T]TGAACCCAGGAGTTG	161436
rs779951316	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88739903	CTGTTAACAACATGG[A/C]AGCTTTGTGCTATCT	161436
rs779980921	snp	C/G	1.69029e-05	0.00290709	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88618228	TATATAAGTATTTAC[C/G]TAGTCCATGTAGCCC	161436
rs779994177	snp	C/T	3.32607e-05	0.0040779	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624986	GCCTTTCCTTTCCCC[C/T]AGTCACGATAAGTCC	161436
rs779998080	in-del	-/GGGCGAAACT			intron-variant	EML5	GRCh38.p7	14:88775203	ACTGTGGTGGCCATG[-/GGGCGAAACT]CCTTTTGCTTGAGAA	161436
rs780004367	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88722714	GAACGCTAAGCTTGT[A/G]GGAATTATTTATATC	161436
rs780049890	snp	C/T	1.71129e-05	0.00292509	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88661698	ATCCCAAATCGTCCC[C/T]GGTAGCTAGAACCAT	161436
rs780050530	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678573	GTACTCATTATAGTA[C/T]TAGCTTTCAAATTTT	161436
rs780051555	snp	C/T	4.96824e-05	0.00498385	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88688406	AGTCCATCCATACAC[C/T]GCACACATCATTGTG	161436
rs780053533	snp	C/T	3.31713e-05	0.00407242	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88685107	CATGTCCTAATGATA[C/T]GGCACGTATAGATGG	161436
rs780061811	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88727912	GATAACTAGAAGATA[A/C]CCATTGTTTGAAAAT	161436
rs780062598	snp	C/T	3.28812e-05	0.00405457	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88705538	AATCCAGTTCTGGAA[C/T]ATCAGACAGATCTGA	161436
rs780066810	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88634946	TCTGTCTCCAGGGAA[G/T]AATTAGATCTAAACC	161436
rs780068714	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88755593	ATTTGATAATTTTTT[C/T]TATATGTCAATTTAC	161436
rs780073695	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88678022	CACTATTCACAATAA[C/T]AAAGACATGGAATCA	161436
rs780078942	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88688035	ATGACCACACCACTG[C/T]GCTCCAGCTTGGGTG	161436
rs780090455	in-del	-/GG			intron-variant	EML5	GRCh38.p7	14:88758046	TTTTTTTGTAGAGAT[-/GG]GGTCTCCCTATGTTG	161436
rs780091461	in-del	-/AATAC	1.72221e-05	0.00293441	intron-variant	EML5	GRCh38.p7	14:88685188	ACATACAGTTACTAT[-/AATAC]AACAGTGTATATATT	161436
rs780104475	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88673757	CAGAGAGCCAAATCA[G/T]GAATGAATTCCTGTT	161436
rs780110913	snp	A/G			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766607	TTCATTAGCAATTTT[A/G]ATTTCGCCCCAGTCC	161436
rs780129412	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88730243	GATACAAATATACAT[C/T]ACCAGACTAAGCACT	161436
rs780168323	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88625978	TCCAGATGAGATGGA[A/G]TAAAGTGAGAGGAGA	161436
rs780184492	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88715306	AGTGTTTATAAACTA[C/T]AAAGTAAACATAAAT	161436
rs780203143	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88689133	TTTTCCTATTAATGG[A/T]GATTTAAGTTACTTC	161436
rs780210854	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88728529	CAATTAAGAAAATCA[G/T]AAGGAAGAGAAAATA	161436
rs780221166	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88791124	TGCCCTACCTCTGTT[C/T]GTCCTAGGCATCCTT	161436
rs780222877	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616302	GAAGTCAAAGGCTCT[C/T]ATTAGGAACTATAAT	161436
rs780223323	in-del	-/T			intron-variant	EML5	GRCh38.p7	14:88784479	ATACTGCAGAAATTC[-/T]AAAGGATCATTAGTG	161436
rs780235857	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88771627	ACTCCCTTTATTGTG[C/T]TAACATACTTCAAAG	161436
rs780242492	snp	A/G	1.8907e-05	0.0030746	intron-variant	EML5	GRCh38.p7	14:88740379	TTAAAATACTTAAAT[A/G]TACTTACAGCATGGG	161436
rs780245593	snp	A/G	1.65971e-05	0.00288067	intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616246	TTTGTGTTTTGCCTA[A/G]AAAACAATGACAGAC	161436
rs780252241	snp	A/G	1.83337e-05	0.00302762	intron-variant	EML5	GRCh38.p7	14:88684985	CAATTGTATGTAAAG[A/G]AAAAAAAACAAATTA	161436
rs780261713	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88713998	GCATACCACCATGCC[A/T]GGCTAGTTTTTGTAT	161436
rs780295984	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88771806	TTCCTCTCTAGGCTT[C/T]CTGACTTCACAGTTT	161436
rs780305187	snp	C/G	3.45841e-05	0.00415823	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88702536	ACGCTGTGTGTTTTG[C/G]TGTCGATTATAAATG	161436
rs780321056	snp	A/G	1.79583e-05	0.00299647	intron-variant	EML5	GRCh38.p7	14:88704817	AAGCTAGTAAGTGTG[A/G]ACCAAAATTCAAACA	161436
rs780325725	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631236	TTTTTCTTTTTGAGA[C/T]AAGGTCTCACTCTGT	161436
rs780340334	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88778789	TCTCAAAAACAAAAC[A/G]AAACAAAACAAAGTG	161436
rs780363115	snp	A/T	0.000167602	0.00915277	intron-variant	EML5	GRCh38.p7	14:88621891	AAACTTTCAAAATCC[A/T]CTCTTGTAAATACCT	161436
rs780374014	snp	A/C	3.28348e-05	0.00405171	intron-variant	EML5	GRCh38.p7	14:88726507	TGTATCACTGAAGAT[A/C]AAATTATTATGTGTT	161436
rs780377569	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88691432	ATGGAAAAAGTTTGC[C/T]ACCTTTGGTTCAGAG	161436
rs780406920	snp	C/T	0.000224404	0.0105902	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695437	CTATGCCAACTGATG[C/T]CAAACGTTTCCCATC	161436
rs780408575	snp	A/G	1.66701e-05	0.002887	intron-variant	EML5	GRCh38.p7	14:88627073	CAACAAAATTATCTA[A/G]GTTATTACAAGAACC	161436
rs780409333	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88757547	ACCCAGAGAATGGGA[A/G]AAAATATTTGCAGAG	161436
rs780420626	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88743786	CCTCACTAGACTACA[G/T]ATTTCTTTATGGAAT	161436
rs780427569	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88770529	ACGTTTCTGAAACAG[G/T]GAAAAAAGAGTGGGA	161436
rs780429900	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88620237	ACACGGAAGTACTCC[A/G]TAAATGGTAGCCACT	161436
rs780430343	snp	C/T	4.97533e-05	0.0049874	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88642970	TTTAAATAGTGAACA[C/T]TATTCCTACAGTCTC	161436
rs780434623	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88702231	GCTATGAGTTCCAAA[C/T]TTAAATTAAAATAAT	161436
rs780439738	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88671245	TCAGGAGACACTAGG[A/G]GCCAATATTCAACAT	161436
rs780451094	snp	A/T	3.34219e-05	0.00408777	intron-variant	EML5	GRCh38.p7	14:88621346	ATGTAATACAACAGC[A/T]GCTTTTCTTCTTCAT	161436
rs780454287	snp	A/C	0.000497413	0.0157626	intron-variant, synonymous-codon	EML5	GRCh38.p7	14:88616708	AAACTGATAATAGTA[A/C]ACAAAACACAAACTT	161436
rs780459445	snp	C/T	3.31702e-05	0.00407235	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88658226	CGGATTCTTCACTAT[C/T]ACAAGGCCTTTTTTC	161436
rs780481815	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88692255	GGTGGCGGGCACCTG[C/T]AATCCCAGTTACTCA	161436
rs780498530	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88785156	ACTGAACTAATGGAC[A/G]TAGAGTAGAAGGATG	161436
rs780499874	snp	C/T	1.6806e-05	0.00289875	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88712425	AAGGCCTGAAACACA[C/T]GTCCATGAAGCCCAA	161436
rs780505126	snp	C/T	1.89199e-05	0.00307564	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88627739	AGCTGACTGAACATA[C/T]TCCCTTTGAATGGTA	161436
rs780529635	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88761183	TGCACTGGCTTGAAC[C/T]TCTAGCAGGATGTTG	161436
rs780542371	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88670863	ATACACTACAAGATT[-/AG]AGAAAAAAAAAAAGG	161436
rs780547554	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88687809	CCTGGCTGGCACCAT[A/G]GCTCATGCCTGTAAC	161436
rs780551522	in-del	-/TACA			intron-variant	EML5	GRCh38.p7	14:88773196	GGCACTGGGTCATAG[-/TACA]TACACCTCACTTGAT	161436
rs780551790	in-del	-/AGC	2.12804e-05	0.00326187	intron-variant	EML5	GRCh38.p7	14:88618606	AACACGAAATGTAAA[-/AGC]AGAAGAACTTGCCAC	161436
rs780553014	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88665865	GTGAGCTATGATTGC[A/G]CCACTGCACTCCAGC	161436
rs780559995	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88719807	CCTTCACAAAGGAGA[C/T]AGACACATGAAAATC	161436
rs780582719	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88786071	TTCCTCAAAAATACT[A/G]GCATTCTGCTTCAGG	161436
rs780596506	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88721502	AACAAACCTGACAAA[A/G]ACAAGCAAGGGGGAA	161436
rs780600310	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88719571	GAGGAGTTTGCTGTT[C/G]ATAACACAGTGTAGC	161436
rs780601982	snp	C/T	1.65699e-05	0.00287831	intron-variant	EML5	GRCh38.p7	14:88620720	AAGTTAAATCAAGTA[C/T]ATACTAGAAACTCTA	161436
rs780617055	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88618135	GAAACTCAATTACTA[A/T]TCCTTATTGGAATGG	161436
rs780649697	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88709515	GGTTAACCTCATTTG[C/T]AGTCAGACAAATGGA	161436
rs780659000	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88672421	AGGGAAATGTATAGC[C/T]CTAAATGCCCACATC	161436
rs780661910	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88735746	CCTGTATTTCTAAAA[C/T]ACACAAAACTGGAGG	161436
rs780676445	snp	C/T	1.78905e-05	0.00299081	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88695416	GCACAACAGTATGGC[C/T]ATCATCTATGCCAAC	161436
rs780716588	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88655537	CCCTAAAAGAAAACC[C/T]AGCTAATACCATTCA	161436
rs780722067	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88709694	TCTCCATGACCCAGA[A/G]ATTTCACTCCTAGTT	161436
rs780727465	snp	C/T	1.6641e-05	0.00288448	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88712343	CTAAAACTTGGCCAA[C/T]ATAATTTCCATCTAC	161436
rs780729082	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88790208	AGTATCATATTAAAT[C/T]TGTGCCACCAATTTC	161436
rs780753469	snp	C/G	6.36051e-05	0.00563902	synonymous-codon, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706422	ATATTTTCTAAACTT[C/G]GCCCCTATAATAAAA	161436
rs780755498	snp	A/G	1.65715e-05	0.00287845	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88740466	AGTGCACCAGAATAT[A/G]TTAATTCATCCCTTG	161436
rs780788450	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88624396	TCATGTTTCAACATG[C/T]ATATGACTATGTTGG	161436
rs780788833	snp	A/C	1.98014e-05	0.00314647	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88687274	CTTGAGACATCTTTC[A/C]AAAGAGTCATCCCAA	161436
rs780791722	snp	A/G	1.66543e-05	0.00288563	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88664527	ATGGGTTATGTAACT[A/G]GTAGCTCCTTTGCAT	161436
rs780797264	in-del	-/AAGAC			intron-variant	EML5	GRCh38.p7	14:88763137	TTCAAAAGCTAGCAG[-/AAGAC]AAGAAATAACTAAGA	161436
rs780805165	snp	C/T			intron-variant, utr-variant-5-prime	EML5	GRCh38.p7	14:88765465	ATCAGCAACGGCACA[C/T]TGAGTTCTTCTCAAG	161436
rs780829670	snp	A/G	1.7789e-05	0.00298231	intron-variant	EML5	GRCh38.p7	14:88618208	GTCAGTTCTTGCCTT[A/G]TGAATATATAAGTAT	161436
rs780832437	in-del	-/TTG			intron-variant	EML5	GRCh38.p7	14:88780381	GCACAAAGGGTAGAT[-/TTG]TTGTTTACTGTTCAG	161436
rs780836597	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88659058	TATTTTCCTTTTAAA[C/T]AACAATAAAGTTTAA	161436
rs780843569	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88644269	AAAATTAAGAGAAAC[-/AG]AGAATATCCATCCAA	161436
rs780845326	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88633455	AATCCATGCTTCACT[A/G]TGCCTTAAAAGTGTG	161436
rs780848240	in-del	-/AG			intron-variant	EML5	GRCh38.p7	14:88703304	CTGAAACTAAGTAAC[-/AG]TAACTATCTGCAGAG	161436
rs780871866	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638549	AAATTCCTGCTAAAG[A/G]ACTAAATCCAACTAT	161436
rs780900976	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88656613	CCAGAACTTAAAGTA[C/T]AATTAAAAAAAAGTG	161436
rs780902811	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88773112	TTGATCTTTTAACAA[C/T]CCAGTTTACCTTTAA	161436
rs780916023	snp	A/G	1.65999e-05	0.00288091	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88694368	TTTATCAGGCACATA[A/G]GGGTTCATCTTTACA	161436
rs780917188	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88723879	CTTTACCCTGGCATA[A/C]CACCTTATATACTAA	161436
rs780919545	snp	A/G	0.000100464	0.00708673	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88624970	AGAAAGAGGACTCAC[A/G]GCCTTTCCTTTCCCC	161436
rs780941617	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88618590	TTAAATGCATTCACT[-/A]AACACGAAATGTAAA	161436
rs781017277	snp	A/T	3.31752e-05	0.00407265	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88627027	TTGATTGTGACCAGC[A/T]CTGCTGGCAATTTTG	161436
rs781036520	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88658904	GAAAGGATACACATG[C/T]CTATGTACAGCATGA	161436
rs781041007	in-del	-/ATG	7.46157e-05	0.00610756	intron-variant	EML5	GRCh38.p7	14:88657553	TAACTGAGATCAATT[-/ATG]ATCTTATAAATTGGA	161436
rs781055275	snp	C/T	8.29401e-05	0.00643919	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88644484	CTGGAGTTTCTCTGG[C/T]TGTGGTGGGGCCCTG	161436
rs781062357	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88701928	ATAAACATCATTTCT[C/T]CCCTTCCTTCTCTAA	161436
rs781098410	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88752990	AATCTGTTCGTGTAA[C/G]CTGGTTCTTCCTGGA	161436
rs781100478	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88736790	TGATTGATCCCCACC[C/T]TTCACTTACTTTACA	161436
rs781110372	snp	A/T	1.72615e-05	0.00293776	intron-variant	EML5	GRCh38.p7	14:88644395	AAAAAAGAACTCTGG[A/T]TACATTTCAGTAACA	161436
rs781112285	snp	A/T	1.65743e-05	0.00287869	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88616840	ATCAGCTTTCTCAGC[A/T]TGTCTGGACCAGATT	161436
rs781142686	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88666374	TGGGATTACAGGCAT[A/G]TGCCACCAGGCCTGG	161436
rs781190773	snp	A/G	1.67486e-05	0.00289379	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88702506	GAGAATATCATCATC[A/G]TGACCCAGATAAAAA	161436
rs781235999	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674515	ATCACGAGAACAGCA[C/T]AGGAAAGACCCGCCC	161436
rs781236109	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88647198	AAATCCCGTCTCTAC[C/T]AAAAATACAAAAAAC	161436
rs781243348	snp	A/G	1.81823e-05	0.0030151	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726664	ATTAATGCATGATCT[A/G]CTAGGCTCCATATCC	161436
rs781243761	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88643823	GAAAATGTACATTTC[A/G]TTGACTTTGTAGGAC	161436
rs781245144	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88777427	GTCCTACAAGAAATG[C/T]TAAAGGAAGCACTTC	161436
rs781257172	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88744895	CAAAGTGATGCTCTT[C/T]AGTGATAATGAAGAA	161436
rs781261842	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88686660	GCACAAAAATTTGAA[A/C]ATTTGCTGAGTATGG	161436
rs781266933	snp	C/T	1.72285e-05	0.00293495	intron-variant	EML5	GRCh38.p7	14:88704981	CTTCTTTGTAAACCT[C/T]TAAAAATGTATACAA	161436
rs781277629	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88677566	CCATCTGACAAAGGT[C/T]TAATATCCAGAATCT	161436
rs781280458	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88757309	GGACACATACCTCAA[A/C]CCATATACAAATGTC	161436
rs781293062	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88631625	AATACAAAAAGTTAG[C/T]TGGGCGTGGTGGCAG	161436
rs781294652	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88639359	GGCTGAAGTGTAGGG[A/T]CATGAAGAAGAAAGA	161436
rs781313338	in-del	-/ACA			intron-variant	EML5	GRCh38.p7	14:88777625	ATAAAAATAATAACT[-/ACA]ACAACTTTTTAAGAC	161436
rs781332355	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88743348	CACCATACATTTTTA[C/T]GTATCAAAACATCAC	161436
rs781347042	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88691629	AAATCATAACTTGAA[A/G]TTCTCAAAGCCTAGA	161436
rs781362407	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88788141	GTTTCCAGTAATTCC[C/T]ACCAGAGCTTAAAAA	161436
rs781369283	snp	A/G	3.32369e-05	0.00407644	intron-variant	EML5	GRCh38.p7	14:88621333	ACCAATACAGTGAAT[A/G]TAATACAACAGCTGC	161436
rs781375216	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88638268	TAACAGTTTTTCACA[A/G]AGGTAAAAGAATACA	161436
rs781384335	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88616370	CACCGCAGCCAGTGA[C/T]TAGAATGCTTTTCAG	161436
rs781386142	snp	C/G/T	3.52319e-05	0.00419702	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88715096	AATATCAACCGAGCT[C/G/T]TCATTGCATCCAACA	161436
rs781416489	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623496	TGTGATCTCGGCTCA[C/T]TGCAACCTGTGCCTC	161436
rs781416519	snp	A/G/T			missense, upstream-variant-2KB, nc-transcript-variant	EML5	GRCh38.p7	14:88792406	TATACGATCTCCTTG[A/G/T]CCGCAGTGTAGTAGA	161436
rs781439144	snp	A/G	9.96181e-05	0.00705685	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88714988	ATCATTTGTCTGCAA[A/G]TATCTACTGTCTGAA	161436
rs781471908	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88781178	TACAAATACAATGCT[C/T]ATGCTGTTTTCTGTG	161436
rs781490994	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88717719	GAGATCCTGCCACTG[C/T]ACTCCAGCCTGGGTG	161436
rs781515461	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88756281	TTATCTCAATAGACA[C/T]AGAAAAATTATTTGA	161436
rs781527296	snp	A/T	2.29999e-05	0.00339108	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88657500	TAACATCACTGTCAT[A/T]GCCTACAATAAAAAT	161436
rs781533241	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88627485	TCCACTGGGCTTTTA[A/C]AGTGAAATATACCTA	161436
rs781550560	snp	C/T			missense, nc-transcript-variant	EML5	GRCh38.p7	14:88726593	CAAGGGCAAGATGGA[C/T]TCCATCTGCATTGAC	161436
rs781550962	snp	C/T	2.49001e-05	0.00352837	missense, intron-variant, nc-transcript-variant	EML5	GRCh38.p7	14:88706411	GAATGGCCAATATAT[C/T]TTCTAAACTTGGCCC	161436
rs781554104	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88652558	ATGGCCACAAATTCG[C/T]TTGAATTTTCTACAA	161436
rs781576756	snp	G/T	1.68349e-05	0.00290123	intron-variant	EML5	GRCh38.p7	14:88684975	TTGAAATAATCAATT[G/T]TATGTAAAGAAAAAA	161436
rs781590267	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88629884	GTAACTTTTCACTAC[C/T]GTTTTTCACTCTTAG	161436
rs781601534	snp	G/T			intron-variant	EML5	GRCh38.p7	14:88728020	AGTTATAAAACTGCT[G/T]AAAATCAAAACTTGT	161436
rs781603806	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88713007	AATGAAAAACTTTTG[A/G]GGAGATGCATTAATT	161436
rs781608905	snp	C/G	1.65979e-05	0.00288074	missense, utr-variant-3-prime, nc-transcript-variant	EML5	GRCh38.p7	14:88616228	CGAATGACCCAAGAA[C/G]CTTTTGTGTTTTGCC	161436
rs781657444	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	ZC3H14, EML5	GRCh38.p7	14:88613900	CCTCGTTGCTGGCTG[A/G]TACAGCGAGGTGGTC	161436
rs781661230	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88682593	ACTCCGAGACTGATG[C/G]AACCAAGAACACTAG	161436
rs781676451	in-del	-/A	1.98198e-05	0.00314794	intron-variant	EML5	GRCh38.p7	14:88618642	GTATACAGTATTGGT[-/A]ACTGTACCTGGAGAT	161436
rs781679195	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88690629	AGAGGTGGTTTAGCA[C/T]AGAAGATGACAAATT	161436
rs781688066	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88742759	AGCCTTTTTGGTATT[-/A]AATATTTGTCAAAAA	161436
rs781689109	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88744315	CTTCAAACACTACTG[A/G]AGTAAAATTTAACAC	161436
rs781706117	snp	C/G	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant	EML5	GRCh38.p7	14:88685075	TTCACCATTCTTTGT[C/G]CCAACTAAAATATGA	161436
rs781717263	in-del	-/TC	1.71537e-05	0.00292857	intron-variant, downstream-variant-500B	EML5	GRCh38.p7	14:88622562	CAGTAATAACCACTT[-/TC]TGTTTTCTGCTGCAC	161436
rs781745507	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88669552	CTGCAGGAATTTCAG[C/G]AACTCCAGCCAGAGG	161436
rs781747691	in-del	-/ACT	0.00296138	0.0383656	intron-variant	EML5	GRCh38.p7	14:88715218	AAAGAAAAAAATGAG[-/ACT]ACATGAACAGAAGTC	161436
rs781761980	snp	A/C	6.46628e-05	0.0056857	intron-variant	EML5	GRCh38.p7	14:88740358	AAGTAATACACATGA[A/C]AGTGTTTAAAATACT	161436
rs781775786	snp	A/G	1.65999e-05	0.00288091	missense, nc-transcript-variant	EML5	GRCh38.p7	14:88738911	GTTTCCCTGAGATCA[A/G]TCACAGTAATTGGTT	161436
rs796087211	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88666597	ACATCTGTATATATA[C/T]GTTTCAGAACCATAT	161436
rs796089752	in-del	-/AA			intron-variant	EML5	GRCh38.p7	14:88620935	ACATCTTCTGCATTT[-/AA]AAAAAAAAAAAAAAA	161436
rs796101337	snp	C/T			intron-variant, upstream-variant-2KB	EML5	GRCh38.p7	14:88766497	CCAGGCTTATTGGGA[C/T]GAGGAAATTCCTGCC	161436
rs796110434	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88724875	AGATGATGATAGTTA[C/G]AGAGATTCCAGAATC	161436
rs796136592	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88772752	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAGGT	161436
rs796154018	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88711943	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	161436
rs796154066	in-del	-/AC			intron-variant	EML5	GRCh38.p7	14:88716763	CACACACACACACAC[-/AC]GGTAGAAGGTAACAG	161436
rs796262002	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88649190	CTGCCACCACACCCA[A/G]CTAATTTATTTTTAC	161436
rs796284312	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88717497	GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	161436
rs796298204	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88630024	ATAATAAAAACTGTA[-/TT]TTTTTTTTTTTTTTT	161436
rs796325702	snp	C/G			intron-variant	EML5	GRCh38.p7	14:88672996	CTTCTGAAACTATTC[C/G]AAACAGCTGAAAAAA	161436
rs796325930	in-del	-/CATAT			intron-variant	EML5	GRCh38.p7	14:88735884	ATATGGAACAAACTC[-/CATAT]CATATATTTGTAAGA	161436
rs796360042	snp	C/T			intron-variant, utr-variant-3-prime	EML5	GRCh38.p7	14:88615941	AGTTGTGCTTTCAGG[C/T]TACATGTGTAATATT	161436
rs796440904	snp	A/G			intron-variant	EML5	GRCh38.p7	14:88663771	AACTCCTGGGCTCAA[A/G]CAGTCCTCCAGCCTT	161436
rs796498483	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	ZC3H14	GRCh38.p7	14:88612781	CTACTGTATTACTTA[-/A]CAGAGTTTTTTTGTG	161436
rs796548710	in-del	-/TT			intron-variant	EML5	GRCh38.p7	14:88630046	TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTTTCGC	161436
rs796576183	in-del	-/AT			intron-variant	EML5	GRCh38.p7	14:88729089	ATATATAAACACATC[-/AT]ATATATATATAACCA	161436
rs796676523	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88693212	TATTGAATTCTTTTG[C/T]AAGTATGAATACTAC	161436
rs796733885	in-del	CTTTG/GT			intron-variant	EML5	GRCh38.p7	14:88729870	CGGTCTTGTTTTTTG[CTTTG/GT]TTTTTTTTTTGTTTT	161436
rs796773372	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88674137	AGCCAGGCATGGTAG[C/T]GCATGTCTGTAATCT	161436
rs796845908	in-del	-/A			intron-variant	EML5	GRCh38.p7	14:88713403	TCTCAAAAAAAAAAA[-/A]TACTAATAGGTAATA	161436
rs796931471	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88710613	TAAAATCTTAAAATA[C/T]TTATATTAATCCATT	161436
rs796945511	snp	A/C			intron-variant	EML5	GRCh38.p7	14:88671790	TAAACCAAAAAAGAT[A/C]AAAAAAGACAAAGAT	161436
rs796953675	snp	C/T			intron-variant	EML5	GRCh38.p7	14:88623187	CACCCAGCTAATTTC[C/T]GTATTTTTAGTAGAG	161436
rs796953944	snp	A/T			intron-variant	EML5	GRCh38.p7	14:88724127	TACAAAAAAAAAAAA[A/T]AGCTTGGCGTGGTGG	161436
rs796957789	in-del	-/G			intron-variant	EML5	GRCh38.p7	14:88729873	TCTTGTTTTTTGTTT[-/G]TTTTTTTTTGTTTTT	161436

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