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

TRIM4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs892752	snp	C/T	0.0923359	0.194016	intron-variant	TRIM4	GRCh38.p7	7:99899044	cttgaatggccccca[C/T]attcttatcacgtca	89122
rs1048705	snp	A/T	0.487684	0.0775019	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891317	CAGTGAGATGGAAAG[A/T]CAAATCCTATTTGTA	89122
rs1138665	snp	A/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896239	ggaccatagggtcat[A/T]gttagggtatgcttg	89122
rs1865472	snp	A/T	0.436265	0.166749	intron-variant	TRIM4	GRCh38.p7	7:99913940	gtcttcattttatag[A/T]taaggaagccttgat	89122
rs2247761	snp	C/T	0.491465	0.0647671	synonymous-codon	TRIM4	GRCh38.p7	7:99903288	GGATGTGAACTATTC[C/T]CTTGAAGCTGTAAAG	89122
rs2247762	snp	A/G	0.484539	0.0865542	synonymous-codon	TRIM4	GRCh38.p7	7:99903276	TTCTCTTGAAGCTGT[A/G]AAGGTGAAGACAGTG	89122
rs2527909	snp	A/C	0.487684	0.0775019	intron-variant	TRIM4	GRCh38.p7	7:99914601	gggaaaggtggcatg[A/C]gatgtgaaacgagat	89122
rs2527911	snp	C/T	0.483636	0.0889627	intron-variant	TRIM4	GRCh38.p7	7:99906002	gtgtgccaccacacc[C/T]ggctaatttttctat	89122
rs2527912	snp	A/C	0.436408	0.16659	intron-variant	TRIM4	GRCh38.p7	7:99902419	tctctactaaaatac[A/C]aaaattagctgagca	89122
rs2527913	snp	A/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99902249	aaaaaacaaacaaac[A/T]aaaaagaaCCATGTT	89122
rs2527914	snp	C/T	0.483345	0.0897213	intron-variant	TRIM4	GRCh38.p7	7:99900522	GAAATGGTAATGACA[C/T]GAATAAATATATATT	89122
rs2527915	snp	G/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99900395	attttgggtgttttt[G/T]tgagggtgattttgg	89122
rs2527916	snp	A/T	0.499587	0.0143711	intron-variant	TRIM4	GRCh38.p7	7:99900334	tgtagactgcccttc[A/T]taatgtgggtgggcc	89122
rs2527918	snp	A/C	0.450105	0.149859	intron-variant	TRIM4	GRCh38.p7	7:99897849	CATTCTGAGAGCACC[A/C]CCCCTGGCAGTGGCC	89122
rs2527919	snp	A/G	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99896890	CAGTCAGGACTGGCC[A/G]GCCAACTGCAGCTGC	89122
rs2527920	snp	C/G	0.449853	0.150196	intron-variant	TRIM4	GRCh38.p7	7:99896257	tgaacccacattcta[C/G]ttggaccatagggtc	89122
rs2527921	snp	C/G	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99895647	tcacaattacgtttg[C/G]agttttcagtacctt	89122
rs2527922	snp	C/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99895133	tccaccttaagacac[C/T]agagaaagaggagca	89122
rs2571994	snp	G/T	0.488545	0.074807			GRCh38.p7	7:99920648	ATTATAGGAAAGGCA[G/T]TATTTGATATTGGGA	89122
rs2571995	snp	C/G	0.43655	0.16643			GRCh38.p7	7:99920468	GTTTCAGCCAATCAC[C/G]GCCGAGCTTCAGCAA	89122
rs2571996	snp	A/G	0.483418	0.0895317			GRCh38.p7	7:99917477	ccaccttggcctccc[A/G]aagtgctgggattac	89122
rs2571997	snp	G/T	0.487684	0.0775019			GRCh38.p7	7:99916794	GGAATGATATGATCG[G/T]TTTTTTTGTTTTAGA	89122
rs2571998	snp	C/T	0.487621	0.0776941			GRCh38.p7	7:99913749	GTTTTCATATACGTA[C/T]AATTTTCTGGTGCTA	89122
rs2571999	snp	A/T	0.487558	0.0778863			GRCh38.p7	7:99913227	CCAGTTTAGATTCCA[A/T]CTGTGGCCAGATTGA	89122
rs2572000	snp	A/G	0.436123	0.166908			GRCh38.p7	7:99911701	ggtagcatttcattc[A/G]cctgctaatgttgtg	89122
rs2572001	snp	A/C	0.297521	0.245442			GRCh38.p7	7:99909730	AAAAAAAAAAAAAAA[A/C]CAAAAAGAAAAAAGA	89122
rs2572002	snp	C/T	0.437118	0.165792			GRCh38.p7	7:99907431	GCAAAGTTAGGGAAA[C/T]GATTAAAAAAGATGA	89122
rs2572003	snp	A/T	0.487621	0.0776941			GRCh38.p7	7:99903690	TGTGACATGAGCAAA[A/T]GCAACCGTCAGAAAA	89122
rs2572004	snp	G/T	0.00874735	0.0655527			GRCh38.p7	7:99902889	AAATTCAGAGGAAGG[G/T]CTCTGTTGGGGGCGA	89122
rs2572005	snp	C/T	0.487621	0.0776941			GRCh38.p7	7:99896407	aacctccatttaacc[C/T]gaatcaaagggcctt	89122
rs2572006	snp	C/T	0.487558	0.0778863			GRCh38.p7	7:99896188	tctgccatacGatac[C/T]ataaaccttaaacca	89122
rs2572007	snp	G/T	0.165289	0.235211			GRCh38.p7	7:99894673	ttttctttttttttt[G/T]gggggggggatggag	89122
rs2572008	snp	A/T	0.487746	0.0773096			GRCh38.p7	7:99893333	CCAAATTTTAGGCTG[A/T]TTGTGAAAACTTGGG	89122
rs2572009	snp	C/T	0.483563	0.0891524			GRCh38.p7	7:99891382	AACGCTTGTTAAATA[C/T]CTTTTGCTAGCCTCT	89122
rs2572010	snp	A/G	0.488606	0.0746142			GRCh38.p7	7:99890920	TCTCCCAGATTTTCA[A/G]TAAAGACTTTCAGGC	89122
rs2897031	snp	A/G	0.0584853	0.160693	intron-variant	TRIM4	GRCh38.p7	7:99898554	TCGTCTTCACCTGCC[A/G]GACACATTCTGTCCC	89122
rs3220811	microsatellite	(CA)22/23/24/25/26	0.593066	0.127205	intron-variant	TRIM4	GRCh38.p7	7:99909127	ACAGATGAATGGATG[(CA)22/23/24/25/26]CTCCTAAAGATTTGG	89122
rs4727439	snp	A/C	0.450105	0.149859	intron-variant	TRIM4	GRCh38.p7	7:99912611	TTTGTTTGCAATTGA[A/C]TTTTAAAAGCATCAA	89122
rs6957718	snp	A/T	0.281841	0.247964	intron-variant	TRIM4	GRCh38.p7	7:99892878	CCACTGCTGCCCAAC[A/T]GATCCTCAGCCAGGC	89122
rs7781442	snp	A/G	0.434976	0.168179	intron-variant	TRIM4	GRCh38.p7	7:99907600	TATGTACTTGCAACT[A/G]CATTGCTTAAGCATG	89122
rs7787525	snp	A/G	0.281841	0.247964	intron-variant	TRIM4	GRCh38.p7	7:99896037	ttattagtatgatta[A/G]atttgtgtctattat	89122
rs7801568	snp	A/G	0.0551013	0.156571	intron-variant	TRIM4	GRCh38.p7	7:99904488	gaaaataaaatgaat[A/G]ctaggtaaaaactga	89122
rs7809747	snp	C/G	0.483418	0.0895317	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918359	atcacttgaggtcag[C/G]agttcgagaccagcc	89122
rs9690545	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914807	CTTTTTCtttttttc[C/T]ttttttctttttttt	89122
rs10236432	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914808	tttttctttttttct[C/T]tttttcttttttttt	89122
rs10245980	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896657	cagcaggaggttgga[A/G]aaaattccacgagtg	89122
rs10246091	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99896749	atgtggggcccaata[A/G]ccactatccttgatg	89122
rs10271594	snp	C/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99912986	TTCAATTATAACTGC[C/T]GCTTTGTGGTCACTG	89122
rs10464605	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99913234	GGCCACAGTTGGAAT[A/C]TAAACTGGGAGGTGA	89122
rs10808114	snp	A/T	0.487621	0.0776941	intron-variant	TRIM4	GRCh38.p7	7:99900876	AAGATTTTCTTTTTA[A/T]CACTGGTTTCCAGCA	89122
rs11539679	snp	C/T			missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919151	TGGGCCCCGTGCCCC[C/T]GGGCCTGTGCGGCCG	89122
rs11539682	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890979	ACTTTAATTTTTATA[C/T]TTTTTGCATCTTACA	89122
rs11980179	snp	C/T	0.283158	0.247791	intron-variant	TRIM4	GRCh38.p7	7:99905919	cgaagccaaggcagg[C/T]ggatcactcgaggtc	89122
rs12536945	snp	C/T	0.0248432	0.108648	intron-variant	TRIM4	GRCh38.p7	7:99895849	TACTAATATACCCAC[C/T]CCAGATCTATtaaca	89122
rs12537676	snp	C/T	0.0356815	0.128715	intron-variant	TRIM4	GRCh38.p7	7:99896972	acttacaagatgagc[C/T]gcaactagggagata	89122
rs12666007	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891346	TGAGTTGTGATGAGA[A/G]TCATATGCAACAGCA	89122
rs12667341	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918188	tagccatacaagcac[C/T]tgaaacgtggatatt	89122
rs12670351	snp	C/G	0.0209421	0.100162	intron-variant	TRIM4	GRCh38.p7	7:99898532	gggctggtagatgca[C/G]ctggggtcgtcttca	89122
rs13232037	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906699	TTTAAAaaaaaacag[C/T]tgggggcggtggctc	89122
rs13232044	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99906706	aaaaacagctggggg[C/G]ggtggctcacacctg	89122
rs13235389	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99907232	aagtgattctcctgc[A/C]tcagcctcccaagta	89122
rs13246364	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99906700	TTAAAaaaaaacagc[G/T]gggggcggtggctca	89122
rs13310326	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893370	ATTAACAAATTCTCA[C/T]GTTGAATCAAAACTA	89122
rs17277546	snp	A/G	0.0333695	0.124785	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891948	TCCCAAAAGCGTCTT[A/G]GAAAATTTCCTGTCC	89122
rs28360802	snp	C/T	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99894430	CAATGCTTTGGGAGG[C/T]CAAGGCAGTGGATTA	89122
rs28477519	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906427	AAACTCCTGAGCTCA[A/G]GAGATCCTCCCATCT	89122
rs28548943	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99909728	CTTCTTTTTTCTTTT[G/T]GTTTTTTTTTTTTTT	89122
rs28847643	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99905036	ACGCTGTCTAAAAAA[A/T]AAAAAATAAAAATTA	89122
rs33998596	snp	C/G	0.113619	0.209524	missense	TRIM4	GRCh38.p7	7:99892245	ACACCTTTTCTTGTT[C/G]TTCTGTCTCACGCCT	89122
rs34083877	in-del	-/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891828	ACGGCAACAAAAACT[-/G]CTGTTTCTTCTACCT	89122
rs34275396	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99905239	GCAACTGGAACTCTT[-/A]ATTTTACACACTGGT	89122
rs34277597	snp	A/T	0.486398	0.0813386	intron-variant	TRIM4	GRCh38.p7	7:99912544	ATTAAAAAAAAAAAA[A/T]AATACCATAAACAAA	89122
rs34293437	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99911819	AAACATGTACCCATA[A/G]ATAGACCTGTACAAG	89122
rs34360797	in-del	-/T	0.450357	0.149522	intron-variant	TRIM4	GRCh38.p7	7:99900709	TGTTTTTGAAGGATA[-/T]TTTTTTGCCAGTTCT	89122
rs34395561	snp	C/G	0.0240643	0.107019	intron-variant	TRIM4	GRCh38.p7	7:99908525	ACATTCAGCTCTAAA[C/G]ACAAGAGAGAGTTCA	89122
rs34402397	snp	C/T	0.00143823	0.0267777	synonymous-codon	TRIM4	GRCh38.p7	7:99892700	TCCCAAACTCGTCTT[C/T]TCCCAGGAAGGGAGA	89122
rs34698695	in-del	-/C			intron-variant	TRIM4	GRCh38.p7	7:99916154	TTTAAGGGCTATGTT[-/C]CCCCTTTCATACCCA	89122
rs34914690	in-del	-/A	0.495407	0.0477027	intron-variant	TRIM4	GRCh38.p7	7:99912531	ATTAAAAAAAAAAAA[-/A]TAATACCATAAACAA	89122
rs34997124	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921463	AGTAGCACCTAGTGT[-/C]CCCTGCACCACCGTT	89122
rs35432946	snp	C/T	0.113882	0.209695	missense	TRIM4	GRCh38.p7	7:99892567	AGATTTCAGCACTTA[C/T]CCTGTGTTCTGGGAA	89122
rs35520899	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99916284	GTTTCCCAAGCTTCT[-/A]CTTTGTGCCTTTTTT	89122
rs35926610	in-del	-/A			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920281	GCAGCACTCAGAACC[-/A]AAAAGAGGTTCAGAG	89122
rs35959826	in-del	-/C			intron-variant	TRIM4	GRCh38.p7	7:99901828	CTGATCAGAACTCTG[-/C]CCAAACAACTAGGAA	89122
rs35997738	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99895932	TGTTTCTTTTCCAGT[-/A]AAAAATTGGGTCTTA	89122
rs36063762	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99911571	TAACAATTACTAATA[-/G]GGTATAACTTTTCAT	89122
rs41280953	snp	A/G	0.0923359	0.194016	intron-variant	TRIM4	GRCh38.p7	7:99902974	GAGTGCTGTGTGTCT[A/G]TCTCTCCAATGTGCT	89122
rs56337108	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897913	CCTTTCTTGTACCCA[C/T]TAAACATCTCACCTG	89122
rs56337765	snp	C/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99893172	CTGGGGAGGCTGAGG[C/G]AGAAGAATCACTTAA	89122
rs57028043	snp	A/G	0.0337553	0.125452	intron-variant	TRIM4	GRCh38.p7	7:99898208	TCCACCTAGTATGGG[A/G]GCAGGTTAGTGCTAC	89122
rs57128906	snp	A/T	0.0391387	0.134304	intron-variant	TRIM4	GRCh38.p7	7:99904351	AAATACCTGACCAAC[A/T]CTCCTCAAAACTTTC	89122
rs57799977	in-del	-/TAAA/TAAATAAA			intron-variant	TRIM4	GRCh38.p7	7:99913697	AAATAAATAAATAAA[-/TAAA/TAAATAAA]AATAATAATTTTTTT	89122
rs57960671	in-del	-/TGTGTG/TGTGTGTG	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909158	GTGTGTGTGTGTGTG[-/TGTGTG/TGTGTGTG]CGTGTGTGTGTGCAT	89122
rs58242927	in-del	-/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909750	TTTTTTTTTTTTTTT[-/T]GAGACAAAGTCTCAC	89122
rs58730747	snp	C/T	0.0391387	0.134304	intron-variant	TRIM4	GRCh38.p7	7:99914405	AAGCAATCCTCCTGC[C/T]TCAGCCTCCCAAAGT	89122
rs58750403	snp	C/T	0.0333695	0.124785	intron-variant	TRIM4	GRCh38.p7	7:99908282	ATTGTTTAATAATTA[C/T]AAATGTACACATAAG	89122
rs59409421	in-del	-/A	0.5	0	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918574	GAAAAAAAAAAAAAA[-/A]TCTCATTGATAATTT	89122
rs59996356	snp	C/T	0.0629771	0.165899	intron-variant	TRIM4	GRCh38.p7	7:99896882	AAGCTGTGGCAGCTG[C/T]AGTTGGCCGGCCAGT	89122
rs60305755	snp	A/T	0.0391387	0.134304	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890994	CTTTTTGCATCTTAC[A/T]AACTTTCTACAATAA	89122
rs61742750	snp	G/T	0.00972114	0.0690367	missense	TRIM4	GRCh38.p7	7:99903241	CGCTTTAGCATTTCC[G/T]TCATCAATGGTATCT	89122
rs66953435	snp	G/T	0.0240643	0.107019	intron-variant	TRIM4	GRCh38.p7	7:99909177	GTGTGTGTGCATCCA[G/T]TCATCTGTTTCTTTC	89122
rs67670034	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99912544	TTTGTTTATGGTATT[-/A]TTTTTTTTTTTTAAT	89122
rs67842492	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99893371	TAACAAATTCTCACG[-/AT]TTGAATCAAAACTAG	89122
rs71108462	in-del	-/AT	0	0	intron-variant	TRIM4	GRCh38.p7	7:99893370	TAGTTTTGATTCAAC[-/AT]GTGAGAATTTGTTAA	89122
rs71276830	in-del	AGAAATATGAAGAAACCC/TA	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99900933	TCAACAAACCCTGAG[AGAAATATGAAGAAACCC/TA]TGAGAAATATGAAGA	89122
rs71569524	snp	G/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99894060	AAATCTCACATATTG[G/T]GATTATTATACATTA	89122
rs73156670	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99907783	GTTGTCTCTTGCTTA[C/T]GAAAAAAAAATAGTA	89122
rs73156671	snp	C/T	0.00716266	0.059414	intron-variant	TRIM4	GRCh38.p7	7:99911096	ATGCCTGTGGGACAT[C/T]CAAGTGGATATGTTA	89122
rs73405419	snp	C/G	0.00795532	0.062565	intron-variant	TRIM4	GRCh38.p7	7:99897615	TCGGTTCTTGCACTC[C/G]ATGGGGGAAAGGCCT	89122
rs73405431	snp	A/G	0.0337553	0.125452	intron-variant	TRIM4	GRCh38.p7	7:99907996	ACTTTACCTACAGAG[A/G]ATATAAAGGTAAAGA	89122
rs73405434	snp	A/C	0.0126979	0.078662	intron-variant	TRIM4	GRCh38.p7	7:99909358	CTTCCTCTCCTATCC[A/C]CGTATCTACAAGGGG	89122
rs73711661	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891738	CAAATACAACTAAAA[C/T]TGTCTTATACAATAA	89122
rs73711662	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891803	ATGAAGGAAATTTCA[A/G]CAATTTCACAACGGC	89122
rs73711666	snp	C/T	0.0310518	0.120672	intron-variant	TRIM4	GRCh38.p7	7:99898310	ATGCACCCTTATGTA[C/T]TGAAAGGCATGATAA	89122
rs73711671	snp	A/G	0.0310518	0.120672	intron-variant	TRIM4	GRCh38.p7	7:99901290	TTAAAACTTTGATCT[A/G]GTCTCTATGTACCTC	89122
rs73711677	snp	C/T	0.00597247	0.0543191	intron-variant	TRIM4	GRCh38.p7	7:99912075	GAAAAAAAATCAGAA[C/T]GGTGGTTGCCCTGGT	89122
rs73711681	snp	A/C	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99914645	CTCCAGGTGCAGAGA[A/C]CTTCTTCCTACCCCA	89122
rs74608266	snp	A/C	0.0898077	0.191933	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920398	TTATTTGACAATGAT[A/C]TGATGAGGCATTTGC	89122
rs74857142	in-del	-/TTT			intron-variant	TRIM4	GRCh38.p7	7:99893981	CCTTTTTTTTTTTTT[-/TTT]ACTTTAGTGATATAA	89122
rs74892548	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895784	CTTTATCATTAGGAT[A/G]TAACATTCTTTATCT	89122
rs75227933	snp	A/G	0.0584853	0.160693	intron-variant	TRIM4	GRCh38.p7	7:99911118	GATATGTTAGCAATT[A/G]GAGTTGGGAAGGAGA	89122
rs75316265	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99893278	TCTTTAAAAAAAAAA[A/G]GACTAACCTCTAGAA	89122
rs75457755	snp	A/C/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99912531	TGAGACTCTACATAT[A/C/T]AAAAAAAAAAAATAA	89122
rs75484058	snp	C/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918181	ATCCATTTAGCCATA[C/G]AAGCACCTGAAACGT	89122
rs75567347	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99893277	ATCTTTAAAAAAAAA[A/G]AGACTAACCTCTAGA	89122
rs75571898	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99902177	TTTATTTTAGTTGCT[G/T]CAGACAAGAAAACAA	89122
rs75626924	snp	A/G	0.00953873	0.0683987	intron-variant	TRIM4	GRCh38.p7	7:99906809	TATGAGCACACCACC[A/G]CACTCCAGTCTGGGT	89122
rs76108580	snp	A/G	0.0333695	0.124785	intron-variant	TRIM4	GRCh38.p7	7:99898109	TCTATATTTGGCATG[A/G]TAAGTCTCACCCACT	89122
rs76123023	snp	A/G	0.0123036	0.0774623	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891607	GCAATGCCTGACTGG[A/G]TAGAAAAAGATTCTA	89122
rs76384158	snp	A/T	0.0592355	0.161582	intron-variant	TRIM4	GRCh38.p7	7:99895082	TCTGCTCTGATTTTT[A/T]TTATTTCCATTCTTC	89122
rs76595998	snp	A/C/G	0.00716713	0.0594884	intron-variant	TRIM4	GRCh38.p7	7:99894644	TGCGCCCCAGCCTAG[A/C/G]CAACAGACCAAGACT	89122
rs76638984	snp	A/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918178	AGTATCCATTTAGCC[A/T]TACAAGCACCTGAAA	89122
rs76665876	snp	A/G	0.0091757	0.0671093	missense	TRIM4	GRCh38.p7	7:99892234	AAAATGGCCGGAGGC[A/G]TGAGACAGAAGAACA	89122
rs76817729	snp	G/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909732	TTTTTTCTTTTTGTT[G/T]TTTTTTTTTTTTTTT	89122
rs76972859	snp	A/G	0.0926964	0.194308	intron-variant	TRIM4	GRCh38.p7	7:99899644	ATTTTACTTTTAAAT[A/G]TAAGTTCCAAAATAC	89122
rs77087987	snp	G/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99909746	TTTTTTTTTTTTTTT[G/T]TTTTGAGACAAAGTC	89122
rs77117104	snp	A/C	0.0162398	0.0886349	intron-variant	TRIM4	GRCh38.p7	7:99906453	CATCTCAGTTTCCCA[A/C]AGTGCTGGAATTACA	89122
rs77122277	snp	A/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99912536	CTCTACATATTAAAA[A/T]AAAAAAATAATACCA	89122
rs77179311	snp	A/G	0.0138799	0.0821421	intron-variant	TRIM4	GRCh38.p7	7:99905674	TTGTGACAACCAAAA[A/G]TGTCTCTATATAATA	89122
rs77453126	snp	A/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99912535	ACTCTACATATTAAA[A/T]AAAAAAAATAATACC	89122
rs77473298	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99899579	ACATGAGAACTGTAT[A/C]ATAGTATACTTTCAT	89122
rs77577977	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99895572	AAGTTGATTGATAAT[A/G]TTATTCAAGTCTACT	89122
rs77711029	snp	G/T	0.491936	0.0629843	intron-variant	TRIM4	GRCh38.p7	7:99909731	CTTTTTTCTTTTTGT[G/T]TTTTTTTTTTTTTTT	89122
rs77834981	snp	A/G	0.0926964	0.194308	intron-variant	TRIM4	GRCh38.p7	7:99896985	GCTGCAACTAGGGAG[A/G]TATTAGCTCAGGCTA	89122
rs78082959	snp	C/T	0.0256215	0.110247	intron-variant	TRIM4	GRCh38.p7	7:99910802	GCAAGTCAATCAACA[C/T]TGACAAATTGGGCTG	89122
rs78284200	snp	A/T	0.0310518	0.120672	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918381	AGACCAGCCTGGCCA[A/T]GATGGTGAAACCCCT	89122
rs78599870	snp	A/C/T	0.00162967	0.0285001	missense	TRIM4	GRCh38.p7	7:99892429	CCCAGATGCCCACAT[A/C/T]TGGGGACATTTTTGA	89122
rs78857058	snp	A/C	0.00914312	0.0669923	intron-variant	TRIM4	GRCh38.p7	7:99907787	TCTCTTGCTTATGAA[A/C]AAAAAATAGTAATGG	89122
rs79441984	in-del	-/AA			intron-variant	TRIM4	GRCh38.p7	7:99905061	AAATTAAAAAAAAAA[-/AA]TAGCTTTATCAAGGA	89122
rs79533752	snp	A/G	0.0926964	0.194308	intron-variant	TRIM4	GRCh38.p7	7:99904964	TTGAACCTGGGGGGC[A/G]AAGTTGCAGTAAGCC	89122
rs79672106	snp	A/C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918179	GTATCCATTTAGCCA[A/C/T]ACAAGCACCTGAAAC	89122
rs79810349	snp	C/G	0.0926964	0.194308	intron-variant	TRIM4	GRCh38.p7	7:99902700	ACCTCTACCTTTCCT[C/G]AAAATACACCTTGTT	89122
rs79915538	snp	C/T	0.0919752	0.193722	intron-variant	TRIM4	GRCh38.p7	7:99911028	TAGGAAGAAGAGCAG[C/T]GTGTAAATGGGAGGA	89122
rs111280845	snp	C/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99905465	AAATCATCCAAATTT[C/T]CCTCAAAAGAAAAAT	89122
rs111307420	snp	C/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921446	ACAAAGTAGATGAGC[C/T]GCAGTAGCACCTAGT	89122
rs111526571	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893041	ATCACTGGAGGTCAC[A/G]AGAGTGAGACCAGCC	89122
rs111848151	snp	G/T	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99904735	CTCACTAGTTATCAG[G/T]AAAATGCTTTATCTG	89122
rs112221624	snp	G/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99902782	TGCTGCTGCTTCTGC[G/T]TGAAACAGTCATCCC	89122
rs112247190	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99901347	TTTTAAAGTCCTTCC[A/G]TGCTTATTCTAACAT	89122
rs112346531	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915055	CCTCAAGGGATCCTC[A/G]CGTCTCAGCCTCCCA	89122
rs112374410	in-del	-/C	0	0	intron-variant	TRIM4	GRCh38.p7	7:99916795	TAAAACAAAAAAAAC[-/C]GATCATATCATTCCC	89122
rs112509575	snp	C/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99903700	GTTGCATTTGCTCAT[C/G]TCACATATGATCTCC	89122
rs112701839	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99911019	TAGAAAATATAGGAA[A/G]AAGAGCAGTGTGTAA	89122
rs112782613	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM4	GRCh38.p7	7:99904675	AACCTAAATTGTTCA[C/T]TTTTTTAAAAAAACT	89122
rs112791366	in-del	-/A	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99893268	CAAGATTCTATCTTT[-/A]AAAAAAAAAAGACTA	89122
rs112871293	snp	A/G	0.00337267	0.0409263	intron-variant	TRIM4	GRCh38.p7	7:99903566	CCCATAAGAGAACAG[A/G]AGTGCATACCTGGTC	89122
rs112979582	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99909262	GTAGGAAGGAGAGGG[A/G]TGCTACCTTAAAGTA	89122
rs113130415	snp	C/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921306	TATGAGTATCCTTGC[C/T]AGAGGAGCTGACACT	89122
rs113716901	snp	G/T	0	0	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917818	TTACACCATCAGTAA[G/T]GGGAGGGGGTGGGGC	89122
rs113894613	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99917517	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	89122
rs113980790	snp	A/G	0.5	0	intron-variant	TRIM4	GRCh38.p7	7:99903059	GTAACAGTGCGTTAA[A/G]TAAATGTTTCTTGAA	89122
rs114204935	snp	A/T	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99917024	CACCACATTTGGAAT[A/T]TGCTGTTCCTTTGGC	89122
rs114259666	snp	C/G	0.0185938	0.0946107	intron-variant	TRIM4	GRCh38.p7	7:99905582	TTGCTGGGAGCTGAA[C/G]GCAGGCATGTCCTGT	89122
rs114408406	snp	C/T	0.0248432	0.108648	intron-variant	TRIM4	GRCh38.p7	7:99897057	CACTGGTTTGTTGCA[C/T]AGCCTGTTTGAAGGG	89122
rs114512362	snp	A/G	0.0103295	0.0711199	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921292	TCCAACTTTAAAGAT[A/G]TGAGTATCCTTGCTA	89122
rs114572556	snp	C/T	0.00914312	0.0669923	downstream-variant-500B	TRIM4	GRCh38.p7	7:99889921	AGCATAACTCCAATC[C/T]AATCTCTGCCTCCAT	89122
rs114852114	snp	A/G	0.00676609	0.0577691	intron-variant	TRIM4	GRCh38.p7	7:99912656	TGATGTATTCAGAGA[A/G]ATACAGACAAATGGA	89122
rs115410208	snp	C/T	0.0256215	0.110247	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891134	TGAGGAAAATATACA[C/T]AGTATAAAAAAGTAA	89122
rs115702402	snp	C/T	0.0146672	0.084371	intron-variant	TRIM4	GRCh38.p7	7:99903752	GACAGAATCTGGTCC[C/T]TTCTTTCACGTGGCC	89122
rs115819978	snp	G/T	0.0103295	0.0711199	intron-variant	TRIM4	GRCh38.p7	7:99895809	TTATCTCTGGTAATA[G/T]CCTTTGCTCAGAAAT	89122
rs115928585	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919507	CGAACCGCCGTCACC[A/G]CCTCACGTAAAAGGG	89122
rs115952343	snp	C/T	0.0119091	0.0762411	intron-variant	TRIM4	GRCh38.p7	7:99903463	ATTTTTCCTCAGACC[C/T]CCATTAGGGTGTGCC	89122
rs116112293	snp	A/G	0.0248432	0.108648	intron-variant	TRIM4	GRCh38.p7	7:99912315	GCAGGTGGACAGCTT[A/G]AGGCCAAGAGTTCGA	89122
rs116497166	snp	A/G	0.0154538	0.0865337	intron-variant	TRIM4	GRCh38.p7	7:99912119	AGAGAATAACTGGGA[A/G]AGGGCATGAAAGAAT	89122
rs116526345	snp	A/G	0.0170251	0.090679	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890363	CCCAGCAATCCCATT[A/G]TTCGGTATATGCCCA	89122
rs116587478	snp	C/T	0.0248432	0.108648	intron-variant	TRIM4	GRCh38.p7	7:99914000	CCCAGCTCTTGAGTT[C/T]TATGAATTTCAGTCA	89122
rs116599183	snp	C/T	0.0103295	0.0711199	intron-variant	TRIM4	GRCh38.p7	7:99898369	TGGGGTGGCTACCCC[C/T]ACAGCAATGCAACCA	89122
rs117029319	snp	A/G	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99902840	ATCCCTCAAATCTCA[A/G]AACTGTCGCCTCTGC	89122
rs117360193	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99900848	GTAACTATCCTCTCC[C/G]CTGGTTGCATTTAAG	89122
rs117384638	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894780	ATTCCAGTTATCTCT[A/G]TCTTCATGAGTCAGC	89122
rs117490236	snp	C/T	0.0107246	0.0724382	intron-variant	TRIM4	GRCh38.p7	7:99905517	TAATATAATGGAATA[C/T]GACAGTACTATACAG	89122
rs117578328	snp	A/G	0.0134861	0.0810011	intron-variant	TRIM4	GRCh38.p7	7:99893922	TGTATGCTAGAGTTT[A/G]ACAAATGCTTTTCCT	89122
rs117656934	snp	C/T	0.0584853	0.160693	intron-variant	TRIM4	GRCh38.p7	7:99916474	TACATTCCACAAGCA[C/T]GGGATCTTCTGTCCT	89122
rs117674278	snp	C/T	0.0458787	0.144342	intron-variant	TRIM4	GRCh38.p7	7:99902176	TTTTATTTTAGTTGC[C/T]GCAGACAAGAAAACA	89122
rs118033517	snp	C/T	0.00835141	0.0640778	intron-variant	TRIM4	GRCh38.p7	7:99895419	TGATCAGAGAACATA[C/T]TCTGAATGATCGGAA	89122
rs137963443	snp	A/C	0.00557542	0.0525036	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891275	ATACTGAGCTAGTTA[A/C]TCTAAAGAGTTCAGT	89122
rs138022548	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905155	TGAGGGCAGGAGATG[A/C]CATTTTGCACCTTTC	89122
rs138155062	snp	C/T	3.29473e-05	0.00405864	missense	TRIM4	GRCh38.p7	7:99908704	TCTTCTTCGTCTCTT[C/T]TTCTTCTTTGTTCAA	89122
rs138275683	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912232	TGGTATTAAATTTTA[C/T]CTCAAAAAATACCAT	89122
rs138276586	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921407	TTCTGCCCCATCCCA[A/G]CAAGGTGAACCAGCT	89122
rs138279977	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99893369	ATTAACAAATTCTCA[-/AT]CGTTGAATCAAAACT	89122
rs138338434	snp	C/T	0.00318978	0.0398085	intron-variant	TRIM4	GRCh38.p7	7:99917046	TCCTTTGGCCTGAAA[C/T]ACCTTCTTTCCTACC	89122
rs138409466	snp	G/T	0.0248432	0.108648	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917690	CACCACTGCATTCCA[G/T]CCTGGGCAACAAGAG	89122
rs138636663	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890143	AGGTAGCTCTTCAAC[A/G]TATGTTTTTGGGGAA	89122
rs138659765	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911179	AAGCACAGGTGGCAG[C/T]TGGAGCCTTGGGTGA	89122
rs138664606	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896187	GTGGTTTAAGGTTTA[C/T]GGTATCGTATGGCAG	89122
rs138692069	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99893695	CCTTCAATAGCTAGT[C/T]AGTCACCAAGTCCTA	89122
rs138817966	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99917207	ATTAATGTTGTACAC[A/G]CTTAAGTTCCTTACA	89122
rs139002692	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902080	GTTTCACATTTCTCA[A/G]GAATCACCGTCCTTC	89122
rs139038907	snp	A/G/T	0.000148316	0.00861034	missense	TRIM4	GRCh38.p7	7:99903585	GCATACCTGGTCAAC[A/G/T]CTTCTTTTGGATTCT	89122
rs139083210	snp	C/T	0.00755907	0.0610114	intron-variant	TRIM4	GRCh38.p7	7:99914295	CCCGAATAGCTGGGA[C/T]TACAGATGTGCATCA	89122
rs139121700	snp	A/G	8.25866e-05	0.00642546	stop-gained	TRIM4	GRCh38.p7	7:99908794	TGCTGATTCTCATTC[A/G]CTGACTCTTTATCTT	89122
rs139360113	snp	C/T	0.00993419	0.0697739	intron-variant	TRIM4	GRCh38.p7	7:99896885	CTGTGGCAGCTGCAG[C/T]TGGCCGGCCAGTCCT	89122
rs139506127	snp	G/T	1.67049e-05	0.00289002	missense	TRIM4	GRCh38.p7	7:99892651	CTGAAGAAAACACTG[G/T]CCAAGAACTGGCTGA	89122
rs139655643	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918654	TATATTATTACAATT[A/G]ACGTCACCTCGTTTC	89122
rs139691178	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99902435	GTATTTTAGTAGAGA[C/T]AGGGTTTCACCATGT	89122
rs139777850	snp	C/T	0.0150606	0.0854603	intron-variant	TRIM4	GRCh38.p7	7:99914102	AAACCCCACTGCCAC[C/T]GCTAGTTGAAGCCAC	89122
rs139839742	in-del	-/TTTCTTCATATTTCTCAGGG			intron-variant	TRIM4	GRCh38.p7	7:99900915	GAGCCTTGGCATATT[-/TTTCTTCATATTTCTCAGGG]TTTCTTCATATTTCT	89122
rs139880372	snp	A/G/T	0.00397884	0.0444256	missense, synonymous-codon	TRIM4	GRCh38.p7	7:99908681	TTTTAACGTGTTCTC[A/G/T]TTCAGCTTCTTCTTC	89122
rs139927414	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99902988	TGTCTCTCCAATGTG[C/T]TTACGAACTCATGAA	89122
rs139980143	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891827	CAACGGCAACAAAAA[C/T]TCTGTTTCTTCTACC	89122
rs139998899	snp	C/T	0.0209421	0.100162	intron-variant	TRIM4	GRCh38.p7	7:99907340	GTCTCAAACTCCTGA[C/T]CTCAGGTGATCCACC	89122
rs140032652	in-del	-/GT/GTGT/GTGTGTGT	0.430434	0.173042	intron-variant	TRIM4	GRCh38.p7	7:99909133	TTTAGGAGTGTGAGG[-/GT/GTGT/GTGTGTGT]GTGTGTGTGTGTGTG	89122
rs140157786	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917899	ATCTAAAGGATAGAT[A/G]TGGGTAGAGAAAGAG	89122
rs140270136	snp	A/T	0.0134861	0.0810011	intron-variant	TRIM4	GRCh38.p7	7:99904312	GAAAAAAACAGACAA[A/T]TTCCAATAGGGGAGC	89122
rs140303682	snp	C/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99909938	AGTCTCCCTATGTTG[C/G]CCAGGCTGGTCTTGA	89122
rs140455029	snp	C/T	6.66334e-05	0.00577168	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919395	CCTGGATGTCCTCAG[C/T]TTCCATGCTGCTTCC	89122
rs140523056	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920732	GTATCTGTTTGGGGG[C/T]TATTGATGAAAGTTC	89122
rs140716138	snp	A/G	3.2993e-05	0.00406145	intron-variant	TRIM4	GRCh38.p7	7:99903631	ACATAAGCAAATTAC[A/G]AACCTTCTCCTGGAG	89122
rs140835365	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910878	GGAAGCAGAAATGTT[A/G]GAGAAACACACAAGA	89122
rs141082898	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898541	GATGCACCTGGGGTC[A/G]TCTTCACCTGCCGGA	89122
rs141405683	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911691	GGAACTCTTACACAA[C/T]ATTAGCAGGCGAATG	89122
rs141470627	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916883	ACTATGGCAAACAAG[A/T]TCCTTCATGATAAGG	89122
rs141574557	snp	C/T	1.64814e-05	0.00287061	synonymous-codon	TRIM4	GRCh38.p7	7:99903593	GGTCAACACTTCTTT[C/T]GGATTCTGTGAAAAG	89122
rs141641564	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918241	TGTAAAATACACACC[A/G]ATTTCAGACCTATTA	89122
rs141664999	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895684	GTATTTCTTCTTGCA[G/T]CTCTATTAGTTTTTG	89122
rs141750801	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901258	TGCATTCTTCGCCTT[A/T]ATCACATTTTTCATC	89122
rs141777922	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99901442	TCTTTTTGCATGCAT[A/G]TTTGACTGGATGCCA	89122
rs141890007	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99893563	CCCCTTCTATACTCT[C/T]GGGACTAATCCACTT	89122
rs141894695	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896395	GTACAGAGGATCAAG[G/T]CCCTTTGATTCGGGT	89122
rs142024611	in-del	-/TTTCT	0.389152	0.207694	intron-variant	TRIM4	GRCh38.p7	7:99900934	TTCATATTTCTCATA[-/TTTCT]CTCAGGGTTTGTTGA	89122
rs142235251	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920049	TTTGCTATCCCAAAG[A/G]ACATCCATGGAGGCT	89122
rs142477002	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99909729	TTCTTTTTTCTTTTT[-/G]TTTTTTTTTTTTTTT	89122
rs142778277	snp	A/G	0.0150606	0.0854603	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890957	ATTGAAATGTTAGTA[A/G]TGCATAACTTTAATT	89122
rs143101950	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917790	ATATCAATTCTGCTG[A/G]AGACCACTGGAGTTA	89122
rs143181233	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99905789	ATTCATCTCACAAAC[A/G]TAATGTGAGCAAAAG	89122
rs143253996	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920076	GGCTTTCAACAAATA[A/G]TATGCTCACCTGTTT	89122
rs143421330	snp	C/T	0.0592355	0.161582	intron-variant	TRIM4	GRCh38.p7	7:99894414	CTCATGCCTGTAATC[C/T]CAATGCTTTGGGAGG	89122
rs143468149	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891972	CCTGTCCCATCTCCA[C/T]TGGCCAGACCCACCT	89122
rs143668456	snp	A/G	0.000153988	0.00877328	stop-gained	TRIM4	GRCh38.p7	7:99909600	TCACTTCTACATCCT[A/G]TAAATGCATGACTTT	89122
rs143906902	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907603	GTACTTGCAACTGCA[C/T]TGCTTAAGCATGTTG	89122
rs143939233	snp	A/T	0.00636936	0.0560724	intron-variant	TRIM4	GRCh38.p7	7:99912541	CATATTAAAAAAAAA[A/T]AATAATACCATAAAC	89122
rs144009655	snp	A/C/G	0.00159617	0.0282053	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891666	TTAAGCCTATACTGC[A/C/G]GGATGTTCACACTAC	89122
rs144039788	snp	C/T	0.00953873	0.0683987	intron-variant	TRIM4	GRCh38.p7	7:99910318	TAAATGGGTATAATG[C/T]TACTTCTAATAATCT	89122
rs144290324	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99912620	AATTGAATTTTAAAA[G/T]CATCAAAAGGAAATA	89122
rs144482802	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914242	AGCTCACTGCAGCCT[C/T]GAACTCCTGAGTGCA	89122
rs144561678	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903975	TTACAAGATTGCTTT[C/T]AAATTATAATCGCAA	89122
rs144663712	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99900380	AAATGTTAATCTTAT[C/G]CAAAATCACCCTCAA	89122
rs144840385	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99908980	TTTATACCTACTTGA[C/T]AGCTCTGTCTAGTCA	89122
rs144885495	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM4	GRCh38.p7	7:99899186	AGAATCCAGGAGTGG[C/T]CAACCCAGAAATGCA	89122
rs145184590	snp	C/G	0.00795532	0.062565	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919751	TTGGGCAAGGCGTTA[C/G]AGCCGGACGTTGTGG	89122
rs145207825	snp	A/G	1.64738e-05	0.00286995	missense	TRIM4	GRCh38.p7	7:99892434	ATGCCCACATCTGGG[A/G]ACATTTTTGAACGAT	89122
rs145419408	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99901366	TTATTCTAACATCTG[C/T]GTCAATTCTAGGTCA	89122
rs145490538	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99904990	AAGCCAAGATGGTGC[C/T]ACTGCACTCCAGCCT	89122
rs145514018	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898411	TAGCCAATAATATGT[G/T]GCTAGGGTGGCACAG	89122
rs145581950	snp	A/G	0.00438332	0.0466095	intron-variant	TRIM4	GRCh38.p7	7:99903054	ACCTTGTAACAGTGC[A/G]TTAAATAAATGTTTC	89122
rs146010613	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895994	TGCCTTTTGATTAGC[A/G]CATGCAGACCATTTA	89122
rs146156432	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917798	TCTGCTGGAGACCAC[C/T]GGAGTTACACCATCA	89122
rs146196299	snp	A/G	0.00676609	0.0577691	intron-variant	TRIM4	GRCh38.p7	7:99914243	GCTCACTGCAGCCTC[A/G]AACTCCTGAGTGCAA	89122
rs146275737	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99896692	GACAATGGGATCAGG[A/G]GAGAATCCACGGTGG	89122
rs146288386	in-del	-/T/TT			intron-variant	TRIM4	GRCh38.p7	7:99896746	GTATGTGGGGCCCAA[-/T/TT]TAGCCACTATCCTTG	89122
rs146316052	snp	G/T	0.00102079	0.0225689	synonymous-codon	TRIM4	GRCh38.p7	7:99892463	ATCAGTAATTCCCAT[G/T]ACGTCCTCCCGACAC	89122
rs146700824	snp	A/G	0.0107246	0.0724382	intron-variant	TRIM4	GRCh38.p7	7:99904245	GTAACCAATGGCAAC[A/G]TGTATTTAAAAAATA	89122
rs147009839	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99916963	CCATGCTCCAGAAGT[A/G]CTGAGCAACCTCCAG	89122
rs147045951	snp	C/G	0.0134861	0.0810011	intron-variant	TRIM4	GRCh38.p7	7:99911952	TTGCACCAACCTATA[C/G]AAAAATGGATAAATC	89122
rs147113938	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893593	TCATATGCAGACATC[G/T]TGCCTTCTATGTTCT	89122
rs147278816	snp	A/G	0.000428491	0.0146309	missense	TRIM4	GRCh38.p7	7:99908778	AGCTTTGAAAACTCC[A/G]TGCTGATTCTCATTC	89122
rs147449966	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99906283	TTTTTTTGACTTGGA[C/T]AGTAGTTACATGAAT	89122
rs147646529	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919911	CCTAGGGGCCTGGAA[G/T]GCCAGGAAGACTTGA	89122
rs147711327	snp	C/G/T	0.00104649	0.0228509	synonymous-codon, missense	TRIM4	GRCh38.p7	7:99903303	AGAATAGTTCACATC[C/G/T]TGGATCTCACTCCTA	89122
rs147725446	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99898138	CTTCCCTTCAGCACC[A/C]CCACCACATTATGCA	89122
rs147836848	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918614	TCTCAGCTTTGAATA[A/T]TTGGGGTAATCAGAT	89122
rs147925490	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893432	GCTAGATACACACAG[A/G]TGTCACATAGGACAG	89122
rs148013546	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895063	GTATTTCACTGCAAT[A/G]ATTTCTGCTCTGATT	89122
rs148063847	snp	A/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99901388	TCTAGGTCAGTTTCA[A/G]TTGATTATTTTCCTC	89122
rs148312296	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912719	GTAGAATCTACATGT[A/G]GGTACACTGGTGTTA	89122
rs148475353	in-del	-/AAAT	0.461812	0.168597	intron-variant	TRIM4	GRCh38.p7	7:99913670	GTGAGACTCCATCTC[-/AAAT]AAATAAATAAATAAA	89122
rs148577892	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99909078	ACTTTCACATCTACT[A/G]CTTAGTTTAGCCTTC	89122
rs148752309	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897067	TTGCATAGCCTGTTT[A/G]AAGGGTCACTGACTG	89122
rs148812488	snp	A/G	0.00173618	0.0294122	synonymous-codon	TRIM4	GRCh38.p7	7:99892706	TTCCTGGGAGAAGAC[A/G]AGTTTGGGATGAGCT	89122
rs148827190	snp	C/T	0.0130921	0.0798413	intron-variant	TRIM4	GRCh38.p7	7:99893715	ACCAAGTCCTACCAA[C/T]TCTACCTCTGAAATT	89122
rs149051969	snp	C/G	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99915609	AAGCAGCTTCACCCA[C/G]GGGCAGTTTATGTTT	89122
rs149067205	snp	A/C	0.0475351	0.146656	intron-variant	TRIM4	GRCh38.p7	7:99899878	TCACTGCGGCCTCAA[A/C]CTCCTGGGCTTAAGC	89122
rs149372276	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99917366	TGTTTCCTGTTCATA[A/G]TCAGCTGGTACAACT	89122
rs149511014	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891514	GAGAGAGAGTGCAAC[A/G]TAGGCAGAGTGAGGG	89122
rs149548454	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905635	TCCTACACACAAGAG[A/G]TGCTGGTAGTAACCA	89122
rs149554361	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	TRIM4	GRCh38.p7	7:99908744	AAACAGGTCCTCTTC[C/T]TCAACCAGGAAGTTG	89122
rs149678278	snp	C/T	1.68573e-05	0.00290316	missense	TRIM4	GRCh38.p7	7:99892675	TGGCTGATGCTGTAT[C/T]TTTCACGTATCTCCC	89122
rs149716453	in-del	-/TTT	0.0898077	0.191933	intron-variant	TRIM4	GRCh38.p7	7:99910038	CGCCTGGCAACTTCA[-/TTT]TTTAAGAGCTAAAAG	89122
rs149813794	snp	A/G	0.0154538	0.0865337	intron-variant	TRIM4	GRCh38.p7	7:99908920	TAATCAAACCCTCTT[A/G]AAAAGCTCCTGCCCA	89122
rs149868005	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914404	CAAGCAATCCTCCTG[C/T]CTCAGCCTCCCAAAG	89122
rs149988368	snp	A/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99896916	GACTGTGCTTAGAGC[A/G]GCCCCCAAGGTTGAG	89122
rs150185282	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99917077	TCTACTCACCCTTGA[A/G]GAGCTAACACATTTA	89122
rs150301437	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898628	GCACTTCCAGAAGTG[G/T]GCATTCTGGAGTTGC	89122
rs150426427	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921180	TGTTTCTTTATGTTC[A/G]CAGGGCAAGCAGTTA	89122
rs150500542	snp	C/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918264	ACCTATTATGAAAAA[C/G]GAGTATAAAATATCT	89122
rs150621890	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99901779	GTTTTAGAAGCTTCT[A/G]TCTCCAGCCTTGAGT	89122
rs150674848	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907873	GTGATATGGAGGAAA[A/G]AGAGGTTCTGAGGCA	89122
rs150743321	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890980	CTTTAATTTTTATAC[C/T]TTTTGCATCTTACAA	89122
rs150941537	snp	G/T	1.648e-05	0.0028705	synonymous-codon	TRIM4	GRCh38.p7	7:99903577	ACAGGAGTGCATACC[G/T]GGTCAACACTTCTTT	89122
rs150994864	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910557	GAAAAGAATAAACGT[A/G]TCTATGCGCATACGT	89122
rs151063246	snp	A/G	0.0119091	0.0762411	intron-variant	TRIM4	GRCh38.p7	7:99893117	CAAACAAACAAAAAA[A/G]CTGGCCCGGCATGAT	89122
rs151192287	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99915742	CAGTGACCTGGCTCC[C/T]GAACACCTACGAAGT	89122
rs151242279	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920464	TTATTTGCTGAAGCT[C/T]GGCCGTGATTGGCTG	89122
rs151324191	in-del	-/C			utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919495	CAGACGACTTCCGAA[-/C]CCGCCGTCACCGCCT	89122
rs180807851	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891395	AGATATTTAACAAGC[A/G]TTCAACATTCTCATG	89122
rs180818448	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912857	CACAATACCATCTGT[A/G]CTATTCTGTTTCTAC	89122
rs180842714	snp	A/C/T	0.0023933	0.0345097	intron-variant	TRIM4	GRCh38.p7	7:99915504	AGGATGGGGATATTT[A/C/T]CCATGGATTTAGGGA	89122
rs180845267	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901415	CCTCCATTATGGGTC[A/G]CTGCTTTCCTATCTT	89122
rs180859912	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907718	TTTCTTATTGATAAT[A/T]ACTACTGGGTGGGTC	89122
rs180894186	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920039	TAGCAACCATTTTGC[C/T]ATCCCAAAGAACATC	89122
rs180998204	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99896926	AGAGCAGCCCCCAAG[G/T]TTGAGCTTGTGGCAC	89122
rs181066161	snp	A/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99913372	AATACCAGAAATTTT[A/T]AAAATCACTCTCTCA	89122
rs181314267	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893029	TGAGGCAGGGAGATC[A/C]CTGGAGGTCACGAGA	89122
rs181391079	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99904689	ATTTTTTTAAAAAAA[A/C]TGGTTAATTACCACA	89122
rs181415983	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918367	AGGTCAGCAGTTCGA[A/G]ACCAGCCTGGCCAAG	89122
rs181525934	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900144	GCTACTGACAAGTCC[A/G]AATCTGCTGTGTGAG	89122
rs181561515	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906018	GGTGTGGTGGCACAC[A/G]CCTGTAATCCCAGCT	89122
rs181607507	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900472	GTATAAACTTACCAT[C/T]GCAATTCCTTTTTAA	89122
rs181613442	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918741	GCACACACCCTCTCA[A/G]TATGTTTTTCTTTAT	89122
rs181705142	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99897487	TGAATATGCTAATTA[A/C]CCTGATTTTATCATT	89122
rs181864095	snp	A/G	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99916092	AACTGTGGGTGGTAC[A/G]TAAGAAGTAATGAAC	89122
rs182066032	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890841	AATTGATCTATAGAA[C/T]AAACCTGCACGTGTT	89122
rs182180137	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894198	TCTATGTTCATGAGA[C/G]ACATTGATGTATAAT	89122
rs182190592	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913586	TGAGGCAGGAAAATC[A/G]CTTGAACCCGGGAGG	89122
rs182531807	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907010	ATTAGAAGTGGGTCA[C/T]GGGGTAAAAGTAAAG	89122
rs182577615	snp	A/G	0.00636936	0.0560724	intron-variant	TRIM4	GRCh38.p7	7:99913628	GTGAGCTGGGATCGC[A/G]CCACTGCACTCCAGC	89122
rs182618754	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99916475	ACATTCCACAAGCAT[A/G]GGATCTTCTGTCCTA	89122
rs182845160	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920676	AATAATTTTTCTCAG[C/T]AAGTAGTATGATTAA	89122
rs182853942	snp	C/T	0.0150606	0.0854603	intron-variant	TRIM4	GRCh38.p7	7:99894537	CCAGGCATGGTGGCG[C/T]GCACCTGCAGTCCCA	89122
rs182885987	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM4	GRCh38.p7	7:99898792	GCACATTAATTAAAA[C/T]CAAATGTTGTGTATA	89122
rs182926807	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902196	ACAAGAAAACAACTC[A/G]TTTATTTACTCCATT	89122
rs183141558	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901663	AGATTTTCCTGAGTA[C/T]GCTACTCAGTGCCCG	89122
rs183263774	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99898400	ATCCCTTCAAATAGC[C/G]AATAATATGTGGCTA	89122
rs183267718	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916320	TCTATGTGGTCCTCC[G/T]AGGAGAATCTCATCT	89122
rs183344817	snp	A/G	0.00676609	0.0577691	intron-variant	TRIM4	GRCh38.p7	7:99899156	GAAGACTGTGTATTC[A/G]GAGTTCTGAGCTAAA	89122
rs183467954	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99913404	CTAGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA	89122
rs183582188	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99896609	AGTGCCATCCGTACT[A/G]AAATCAATAGGGGTC	89122
rs183589072	snp	A/G/T	0.00021455	0.0103553	intron-variant	TRIM4	GRCh38.p7	7:99916800	ACAAAAAAAACGATC[A/G/T]TATCATTCCCTGCCT	89122
rs183704238	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99893110	CAAAAAACAAACAAA[A/C]AAAAAAACTGGCCCG	89122
rs183929896	snp	A/C	0.00279162	0.0372561	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890088	ACCTTATCTTGTTTA[A/C]ATCTGCAAATATCCT	89122
rs183936802	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909438	ATGGAGGAAACAGAG[C/G]TTCTGAGGCATCCAA	89122
rs183938931	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910411	ATTATCCACTAATTA[C/G]GAATTATTAAATAAA	89122
rs183980964	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904244	GGTAACCAATGGCAA[C/T]GTGTATTTAAAAAAT	89122
rs184229032	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900246	GCAGTGAAGGCCAAG[A/G]TAGTATGCTTTAGAA	89122
rs184250391	snp	A/C/G	0.000593447	0.0172156	intron-variant	TRIM4	GRCh38.p7	7:99903621	AAGAAGGAAGACATA[A/C/G]GCAAATTACGAACCT	89122
rs184476493	snp	A/G	0.0130921	0.0798413	intron-variant	TRIM4	GRCh38.p7	7:99911384	AATTACAAAACTAGT[A/G]AATAGTGTCAAATGC	89122
rs184534968	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917907	GATAGATGTGGGTAG[A/G]GAAAGAGAACAGACT	89122
rs184604724	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899666	CCAAAATACACCATA[C/T]TTTGTCTGTTGAAAT	89122
rs184658102	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899962	CACTAATTATTTTAT[G/T]TTTTGTAGAGACAGG	89122
rs184714508	snp	A/G	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99906100	CAGTGAGCCAAGATC[A/G]CTCCACTGCACTCCA	89122
rs184755530	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99915123	CCTAGGATAGCACTT[C/T]CTTTTTCTTTCCCAG	89122
rs184948908	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918527	CCAAGATCACGCCAC[C/T]GTGCTCCAGCCTGGG	89122
rs185175569	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912892	ATGTTTCCTAACATT[A/G]TATCATCTATTTACT	89122
rs185217391	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890647	CATCACATGTTCTCA[C/G/T]GTATAAGGGAGAGCT	89122
rs185316821	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99907857	TTTCATCTTCATTCA[C/T]GTGATATGGAGGAAA	89122
rs185340323	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99914519	CAAGATTCTTCACTG[A/G]CTTTCCTCTTCACCA	89122
rs185376539	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891122	AGAAGGGTAGACTGA[A/G]GAAAATATACACAGT	89122
rs185449770	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99895449	ATCCTTTGAATTTGA[C/T]ACTTGCTTTACAGCC	89122
rs185511942	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912597	ACATGCTGAAGTATT[C/T]TGTTTGCAATTGAAT	89122
rs186077836	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920190	CTTTTCTTGTGAATA[A/T]TTGTTTAAAACAAAA	89122
rs186174817	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99897045	ACAAAATGGAGACAC[C/T]GGTTTGTTGCATAGC	89122
rs186203188	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99901486	TATATTGTTAGGTGC[C/T]CTTTTTTTGTTTATT	89122
rs186301877	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900599	TTCCTTCTGTCTGAA[C/G]GACTTCCTTTAAGAC	89122
rs186311047	snp	C/T	0.00119737	0.0244387	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919118	TCCTCGCAGAAGAGC[C/T]GCAGCGGCTCCCAGT	89122
rs186335927	snp	C/G	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99915785	ATTCAGCCCATCCCA[C/G]TGTAACCCTTACCCA	89122
rs186450411	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99913397	CTCTCAGCTAGGTGC[A/G]GTGGCTCACGCCTGT	89122
rs186502791	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99898418	TAATATGTGGCTAGG[A/G]TGGCACAGTAACTGT	89122
rs186509873	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916375	AACAGGCTGAGGATT[A/C]TAAAATATTATCTCT	89122
rs186625110	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893066	CCAGCCTGGCCAACA[C/T]GGCGAAACCCCGTCT	89122
rs186890552	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99916246	GGTCCTCTCCATGTC[G/T]TTTGCTGGCTACCAA	89122
rs186921711	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99894230	CTTTTCTCTTGTGAC[A/G]TCTTTGTCTGATTTT	89122
rs186927849	snp	C/T	0.00795532	0.062565	intron-variant	TRIM4	GRCh38.p7	7:99913594	GAAAATCGCTTGAAC[C/T]CGGGAGGTGGAGGTT	89122
rs187021316	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921588	AGGAAATTCTGGGAA[A/G]CATAGTTTAGCTTAG	89122
rs187076225	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897544	TCACACTGTACCTCA[C/T]AAATATGTAAAATTA	89122
rs187097631	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901710	TGGTGTGGCTGATAG[A/G]AACTGGCACTGTTCC	89122
rs187136992	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890214	GAACTCAGTAGAAAC[C/T]GTTGAATGAGGGGGC	89122
rs187143706	snp	C/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99910960	GATTTAGCCCCTCAG[C/T]TGTGGTTTAAGTAAC	89122
rs187144345	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893165	CCAGTTACTGGGGAG[A/G]CTGAGGCAGAAGAAT	89122
rs187247930	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916842	TATAACTCCCCACTG[C/T]CTGAAAGAGAAAGTT	89122
rs187273255	snp	A/C	0.0596104	0.162024	intron-variant	TRIM4	GRCh38.p7	7:99907353	GACCTCAGGTGATCC[A/C]CCCACCTCAACCTCC	89122
rs187345898	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913439	TTTGGGAGGCCAAGG[C/T]GGGCAGATTACGAGG	89122
rs187483585	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99909131	ATCTTTAGGAGTGTG[A/T]GGGTGTGTGTGTGTG	89122
rs187490347	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899498	CCTTAATGAAGTCAG[C/T]AGGGGACTGGCACAA	89122
rs187734694	snp	C/T	0.00716266	0.059414	intron-variant	TRIM4	GRCh38.p7	7:99903853	CTCCTGGCTTCCTGC[C/T]GGCCTCCCCAACTAG	89122
rs187739383	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902491	ACCTCAAATGATCCG[A/C]CTGCCTCGACCTCCC	89122
rs187787589	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917530	TTCGAGACCAGCCTG[A/G]CCAACATAGTGAAAC	89122
rs187945874	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898860	GAACCCTAGAAACCC[A/G]TATTTCAGTAAAAAT	89122
rs188000176	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99914045	ATTGATCCAAGCTGG[C/T]AGGTGTACTTTGGAA	89122
rs188021204	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99896771	TCCTTGATGGGTGGG[G/T]CCCACCAGGTGAGTA	89122
rs188033322	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915283	GCTGCATCTGGTGCC[A/G]TGCCACAGCATCTGA	89122
rs188235272	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99916582	AACTACCATCCAAGA[C/T]TCCTCTCTCTCTCAC	89122
rs188272733	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99894538	CAGGCATGGTGGCGC[A/G]CACCTGCAGTCCCAG	89122
rs188464488	snp	C/G	0.0023933	0.0345097	intron-variant	TRIM4	GRCh38.p7	7:99892887	CCCAACTGATCCTCA[C/G]CCAGGCCTAGCAGGC	89122
rs188474055	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913062	CCTTCAAATAGGACC[A/C]AGTTTTTGAAAGTTT	89122
rs188711037	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905174	TTTGCACCTTTCAGG[A/G]TGGCTAAAGTTAAAG	89122
rs188783002	snp	A/C	0.000496106	0.0157419	missense	TRIM4	GRCh38.p7	7:99909607	TACATCCTGTAAATG[A/C]ATGACTTTCTTCATC	89122
rs188954713	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99900458	CCAGTCAAGTTGATG[C/T]ATAAACTTACCATCG	89122
rs188964843	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918605	TAATTTTCATCTCAG[C/T]TTTGAATATTTGGGG	89122
rs189315665	snp	A/C	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99895623	CCTAATTATTCTAAA[A/C]ATTATTAAAAGGTAC	89122
rs189348196	snp	C/T	0.00755907	0.0610114	intron-variant	TRIM4	GRCh38.p7	7:99899699	TCAATTATTAGGGTT[C/T]TCCAAAGGAACAGAA	89122
rs189475434	snp	C/G/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99900080	TGTGAGCCACCACAC[C/G/T]CAGCCAGTGTATAAG	89122
rs189663704	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898469	CCTCCCCTTGGGGAT[A/G]GCTACAGGTAGACGG	89122
rs189670072	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99916391	TAAAATATTATCTCT[A/T]GCCTCCAAGGCACCC	89122
rs189753117	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915957	TAGTTCTGTGACCTC[C/G]GGGGCATGTAACCTC	89122
rs189758880	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918040	AATTCAAATGTTACA[C/G]GATTTTCCCAACTGA	89122
rs189847370	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890656	TTCTCACGTATAAGG[C/G]AGAGCTAAACATTGA	89122
rs189996241	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897203	ATAGAGGTTCCCATC[C/T]TCTCAGCATGTCTGA	89122
rs190111197	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911825	GTACCCATAAATAGA[A/C]CTGTACAAGAATATT	89122
rs190277184	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908426	AATTTCCTTTGAATG[A/G]TGAATCTTTGGCTTT	89122
rs190299802	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99906474	TGGAATTACAGACGT[A/G]AGCCACTGTACCTGG	89122
rs190325613	snp	A/C/G	8.97358e-05	0.00669782	intron-variant	TRIM4	GRCh38.p7	7:99902089	TTCTCAGGAATCACC[A/C/G]TCCTTCACTGCCTGA	89122
rs190435975	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912792	TGGTAAAATGAAATA[A/G]GAAAACAAAATTAAA	89122
rs190636801	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99914682	TATCCAGCTCTCCCC[C/T]GCCTCAGGGCCTCTT	89122
rs190928092	snp	C/T	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99907483	TTTTTGTAAACATTC[C/T]GCTGGCTCACATGTA	89122
rs190962195	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99898248	GGGGTATTCCATACA[C/T]GATGGACAAGGGTGA	89122
rs190974374	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916287	TTCCCAAGCTTCTCT[C/T]TGTGCCTTTTTTTAC	89122
rs191080853	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920378	CTAACATCTAGGTGT[C/T]TGCCTTATTTGACAA	89122
rs191120915	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99901573	TTGACCCCTTTGGGT[C/T]TTGCTTTCATGATTT	89122
rs191202803	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919847	GTGTTCGCCTGCTGG[G/T]TAGACCGATTTAAGT	89122
rs191209539	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893621	TCTCTAAGGTGTCAG[A/G]GTCCCCTCCACCTGA	89122
rs191215589	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99913528	AAAAAAAAATTAGCC[A/G]GGCATGGTGGCACAC	89122
rs191241299	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917787	TGCATATCAATTCTG[A/C]TGGAGACCACTGGAG	89122
rs191380095	snp	C/G/T	0.000560019	0.0167248	missense, intron-variant	TRIM4	GRCh38.p7	7:99916758	TCTTCCATTCATCCA[C/G/T]GTGGATGTCAAAGTT	89122
rs191480966	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893077	AACATGGCGAAACCC[C/T]GTCTCTACTGAAAAT	89122
rs191493582	snp	A/G	0.00438332	0.0466095	intron-variant	TRIM4	GRCh38.p7	7:99913596	AAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC	89122
rs191634691	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913398	TCTCAGCTAGGTGCG[A/G]TGGCTCACGCCTGTA	89122
rs191638127	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99909160	TGTGTGTGTGTGTGC[A/G]TGTGTGTGTGCATCC	89122
rs191864705	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890615	TAAGCAAACCAACAC[A/G]TGAACAGAAAACCAA	89122
rs191873639	snp	C/T	0.00597247	0.0543191	intron-variant	TRIM4	GRCh38.p7	7:99911101	TGTGGGACATCCAAG[C/T]GGATATGTTAGCAAT	89122
rs192169150	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899565	TTATACCACTTCACA[C/T]ATGAGAACTGTATCA	89122
rs192175407	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99917476	TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGTG	89122
rs192181427	snp	A/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99899860	CAGTGGTGCAATCAC[A/T]GCTCACTGCGGCCTC	89122
rs192401171	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99903899	CTGCTCCTTTGCGTG[C/T]CTTTTGGTGGGTCCT	89122
rs192471383	snp	A/T	0.00318978	0.0398085	intron-variant	TRIM4	GRCh38.p7	7:99900918	GCCTTGGCATATTTT[A/T]CTTCATATTTCTCAT	89122
rs192555811	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909714	CCAACCATCATCATC[A/T]TCTTTTTTCTTTTTG	89122
rs192621263	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99895839	TCTACTTTGATACTA[A/C]TATACCCACTCCAGA	89122
rs192823235	snp	C/G	0.00438332	0.0466095	intron-variant	TRIM4	GRCh38.p7	7:99895447	GAATCCTTTGAATTT[C/G]ACACTTGCTTTACAG	89122
rs192950303	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99912125	TAACTGGGAAAGGGC[A/G]TGAAAGAATTCTCTG	89122
rs193006106	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899081	CTGGACTGCAGTGTA[C/T]GGCAGACACACCTGA	89122
rs193033970	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99914322	ATCACTACATCCAGC[C/T]AATTTTTGTATTTTT	89122
rs193278743	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902827	CAAACTCCTACTAAT[A/C]CCTCAAATCTCAAAA	89122
rs199938053	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99894684	CCCCAAAAAAAAAAA[-/G]AAAAGAAAAGAAAGA	89122
rs199977056	snp	C/T	0.000214399	0.0103515	synonymous-codon	TRIM4	GRCh38.p7	7:99908621	CTGGCTCTTCTCCCC[C/T]ACCTCTAAGATGAGC	89122
rs200322330	snp	A/G	0.000686012	0.0185077	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919108	CCGCTGGTCGTCCTC[A/G]CAGAAGAGCCGCAGC	89122
rs200387833	in-del	-/ATAC			intron-variant	TRIM4	GRCh38.p7	7:99900932	TTCTTCATATTTCTC[-/ATAC]TCAGGGTTTGTTGAG	89122
rs200389520	snp	A/G	6.58979e-05	0.00573974	missense	TRIM4	GRCh38.p7	7:99908755	CTTCTTCAACCAGGA[A/G]GTTGTGCAGCTTTGA	89122
rs200520150	snp	C/G/T			intron-variant	TRIM4	GRCh38.p7	7:99900933	TCTTCATATTTCTCA[C/G/T]ACTCAGGGTTTGTTG	89122
rs200534198	snp	A/C/G/T	0.000237001	0.0108833	stop-gained, synonymous-codon	TRIM4	GRCh38.p7	7:99892682	TGCTGTATTTTTCAC[A/C/G/T]TATCTCCCTTCCTGG	89122
rs200547987	in-del	-/CT			intron-variant	TRIM4	GRCh38.p7	7:99907202	GGCTCACTGCAATCT[-/CT]GTCTCCCGGGTTCAA	89122
rs200685456	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891816	CAACAATTTCACAAC[A/G]GCAACAAAAACTCTG	89122
rs201008072	snp	C/G	1.68471e-05	0.00290228	intron-variant	TRIM4	GRCh38.p7	7:99903345	AAGACTGCTCTTAGG[C/G]GACAACTAGGGTAGC	89122
rs201126235	snp	C/G	8.23621e-05	0.00641672	missense	TRIM4	GRCh38.p7	7:99892516	TATCTCTACTCTCAA[C/G]TTCCCAGTAATGTTT	89122
rs201165325	snp	A/G	0.000198992	0.00997278	synonymous-codon	TRIM4	GRCh38.p7	7:99909580	CTTCCACTGTGTGGC[A/G]TTCTTCACTTCTACA	89122
rs201183043	in-del	-/G	0.0150606	0.0854603	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890189	AACAGCAAATATCCT[-/G]GGAAGTTGAGAACTC	89122
rs201191696	snp	G/T	8.52915e-05	0.00652981	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918999	ATAGTCACCGCGACG[G/T]CCAGCTCACCCGGTA	89122
rs201293187	snp	A/G	0.000194307	0.00985473	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919124	CAGAAGAGCCGCAGC[A/G]GCTCCCAGTGGCGGC	89122
rs201446854	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99909159	GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGCATC	89122
rs201510808	snp	A/G	3.32939e-05	0.00407993	missense	TRIM4	GRCh38.p7	7:99892635	GCAAAGTAGTTCCAT[A/G]CTGAAGAAAACACTG	89122
rs201644203	in-del	-/C			intron-variant	TRIM4	GRCh38.p7	7:99894663	AGACCAAGACTCCAT[-/C]CCCCCCCCCAAAAAA	89122
rs201685946	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99897472	AAATGTTTGAGGTGA[G/T]GAATATGCTAATTAC	89122
rs201741037	snp	A/C	0.00056339	0.0167743	synonymous-codon	TRIM4	GRCh38.p7	7:99909628	TTTCTTCATCTTGGC[A/C]ACGAGATTACGCTGA	89122
rs201814883	snp	C/T	4.94735e-05	0.00497336	missense	TRIM4	GRCh38.p7	7:99892273	TGTGCAGGTGCACTC[C/T]GTCCACAGCGCTGTA	89122
rs201955132	snp	A/G	6.72993e-05	0.00580044	intron-variant	TRIM4	GRCh38.p7	7:99903343	AGAAGACTGCTCTTA[A/G]GGGACAACTAGGGTA	89122
rs201965995	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	TRIM4	GRCh38.p7	7:99908657	CAATGAAGCGATAGT[C/T]TGATTGAGTTTTAAC	89122
rs201996639	in-del	-/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917772	GTTCATGTACTTACT[-/G]GCATATCAATTCTGC	89122
rs202173362	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99909723	ATCATCTTCTTTTTT[C/T]TTTTTGTTTTTTTTT	89122
rs202208817	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912478	AAGGTTTCAGTGAGC[C/T]GAGATCACACCACTG	89122
rs202245014	in-del	-/GGACACAAAAAA	0.0248432	0.108648	cds-indel	TRIM4	GRCh38.p7	7:99890680	ACATTGAGTACCCAT[-/GGACACAAAAAA]GGGAACAACAGACAC	89122
rs267601667	snp	A/C/G	3.46472e-05	0.00416204	TRIM4	7	allele_origin=G(germline)/A(somatic)	7:99892714	AGAAGACGAGTTTGG[A/C/G]ATGAGCTGTGTCTTC	89122
rs367623110	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919797	ACCGGGGAGGTGCCT[A/G]TGATCTTTCTTTCCA	89122
rs367662743	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99895527	GTAGTATATAGCTGT[C/T]GGGTAGAGTGTTCTA	89122
rs367762588	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99897346	GGAAATGGTGAAGCT[A/G]GGAAGTAAGTTCAAA	89122
rs367835499	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99898779	CTGGGTGGAAGCTGC[A/T]CATTAATTAAAACCA	89122
rs367887507	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99900946	CATACTCAGGGTTTG[C/T]TGAGCATCTTGGATC	89122
rs367924591	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99913118	TAATAATCTACTAAA[C/T]AGAGATTTTCTATGT	89122
rs367926968	snp	A/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890286	ATAAGAAGGGGAGGA[A/G]GGGAGGAGGAGTTAG	89122
rs368014413	snp	C/T	3.29462e-05	0.00405857	missense	TRIM4	GRCh38.p7	7:99892534	CCCAGTAATGTTTCC[C/T]TGAGGTGAAAACGTT	89122
rs368130614	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891866	ATTCCTGTGTTCTCA[A/G]TTCCAATATGGCTGC	89122
rs368392933	in-del	-/ACT			intron-variant	TRIM4	GRCh38.p7	7:99907895	TCTGAGGCATCCGAT[-/ACT]CAACATGAATTATTT	89122
rs368393126	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905280	TAAACTGGAACAATC[A/G]CTTTGTACCAGTTTG	89122
rs368423262	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920333	CTGCTAGCTTTTATA[A/G]GAAGCAAAGTAGAGA	89122
rs368498146	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99892784	GTAGTGCAGCAGCTT[A/G]TCATCAACCCTTCCC	89122
rs368508476	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99904586	GAACTATATTAACAC[A/T]AGATGTTGACAATAG	89122
rs368545704	snp	C/G	0.000153988	0.00877327	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919427	TGCCGCGGAGACGGA[C/G]TCCGACGTGAGGCGC	89122
rs368717124	snp	C/G	1.64798e-05	0.00287047	intron-variant	TRIM4	GRCh38.p7	7:99903558	CCCAGGTCCCCATAA[C/G]AGAACAGGAGTGCAT	89122
rs368772685	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99894670	AGACTCCATCCCCCC[C/G]CCAAAAAAAAAAAGA	89122
rs368949940	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897904	ATGGCTTCCCCTTTC[C/T]TGTACCCACTAAACA	89122
rs369025688	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891690	ACACTACGTCCCTTT[A/G]GTGCAGTTACGGTAC	89122
rs369035666	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99915446	TTTATGAAGCTATTT[A/C]TCTTTCTCTTTTCTC	89122
rs369061930	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901493	TTAGGTGCTCTTTTT[C/T]TGTTTATTTCTACCA	89122
rs369230261	snp	A/G	1.72335e-05	0.00293538	intron-variant	TRIM4	GRCh38.p7	7:99909677	TGCCAGCAGAAACAC[A/G]CACAGGTAAGAAAAC	89122
rs369241114	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909921	ATGTTTCGTAGAGAC[A/G]AAGTCTCCCTATGTT	89122
rs369363025	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896737	TTGTCCACATGTATG[C/T]GGGGCCCAATAGCCA	89122
rs369610109	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99893614	TCTATGTTCTCTAAG[A/G]TGTCAGAGTCCCCTC	89122
rs369611332	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99908572	TCACCCCCACTCGTA[A/G]CTGTCTCACCTGAAG	89122
rs369675920	snp	C/T	0.000153988	0.00877328	missense	TRIM4	GRCh38.p7	7:99892471	TTCCCATGACGTCCT[C/T]CCGACACACCCCAAC	89122
rs369816367	snp	C/T	1.79845e-05	0.00299865	synonymous-codon	TRIM4	GRCh38.p7	7:99892166	GGAAGAAAAGCCTCA[C/T]TTCCTATCAGTCACT	89122
rs369963284	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902263	TAGTTTGTTTGTTTT[C/T]TGAGACAGAGTCTCA	89122
rs370107280	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919994	TCTGAGATGCAGATA[C/T]ATTGCCTTTTTGGTA	89122
rs370168345	snp	A/C/T	0.00535709	0.0514841	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919264	TTCGGGGCAGGGGAA[A/C/T]GGGCCGCCGCCCGGC	89122
rs370272153	snp	A/G	5.3903e-05	0.00519121	intron-variant	TRIM4	GRCh38.p7	7:99902124	TGGTGCTTTGAAAAC[A/G]GTTGTTTCACATATT	89122
rs370407788	in-del	-/A			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918566	GAGACTCCATCTCAG[-/A]AAAAAAAAAAAAAAT	89122
rs370444448	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99895450	TCCTTTGAATTTGAC[A/G]CTTGCTTTACAGCCA	89122
rs370532553	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898620	AAAGCCAGGCACTTC[C/T]AGAAGTGTGCATTCT	89122
rs370713921	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913544	GGCATGGTGGCACAC[A/G]CCTGTAATCCCAGCT	89122
rs370775904	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896752	TGGGGCCCAATAGCC[A/G]CTATCCTTGATGGGT	89122
rs370781205	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912222	GTGTTTTTCATGGTA[C/T]TAAATTTTACCTCAA	89122
rs370829745	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912019	ACAATGGAATTCCAT[C/T]TATATGAAGTTCTGG	89122
rs370852015	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99911468	AAAAAATTAAAAAAA[G/T]TAAAAATAAATTTAA	89122
rs371074357	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99895045	GGTTTCTGTTGGCTT[C/T]CTGTATTTCACTGCA	89122
rs371077279	snp	A/C	0.000193981	0.00984647	intron-variant	TRIM4	GRCh38.p7	7:99903166	ACTTCTCTCTTTATT[A/C]TCCTATTTGAAAGAT	89122
rs371222863	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899110	GACAGCAGTAACTCC[A/C]GCACACCCTGAGAAT	89122
rs371305209	snp	C/T	3.3089e-05	0.00406736	synonymous-codon	TRIM4	GRCh38.p7	7:99908801	TCTCATTCGCTGACT[C/T]TTTATCTTATCCTAA	89122
rs371342093	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906452	CCATCTCAGTTTCCC[A/G]AAGTGCTGGAATTAC	89122
rs371473702	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99905543	TACAGCGGGCACTAC[C/T]GACATTTTGGGCTGG	89122
rs371479368	multinucleotide-polymorphism	AA/TG			intron-variant	TRIM4	GRCh38.p7	7:99895544	GGTAGAGTGTTCTAT[AA/TG]ATAATGGGATCAAGT	89122
rs371480222	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99911094	AGATGCCTGTGGGAC[-/A]TCCAAGTGGATATGT	89122
rs371571216	snp	A/G	1.90751e-05	0.00308823	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892137	TGGACTACAGGGAAG[A/G]AGTTTTGGTCAGGGG	89122
rs371606014	snp	G/T	0.000545751	0.0165099	intron-variant	TRIM4	GRCh38.p7	7:99908552	TTCAGTTAGTGAAGA[G/T]GAGATCACCCCCACT	89122
rs371639163	snp	C/T			synonymous-codon	TRIM4	GRCh38.p7	7:99892205	GACTAAAGATGCTAA[C/T]GGACTCAACCAAAAA	89122
rs371660284	snp	A/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890367	GCAATCCCATTATTC[A/G]GTATATGCCCAATAC	89122
rs371711542	snp	C/T	4.25777e-05	0.00461379	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919018	GCTCACCCGGTAGCT[C/T]TCGAAGGCCTCGTCG	89122
rs371969809	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893664	TTAAATCTTTATTTT[C/T]GACTCTTTCCTCTAA	89122
rs372112864	snp	A/G	0.000284464	0.0119227	intron-variant	TRIM4	GRCh38.p7	7:99903319	TGGATCTCACTCCTA[A/G]GAAGGTAGAGAAGAC	89122
rs372185941	snp	C/T	3.92511e-05	0.0044299	intron-variant	TRIM4	GRCh38.p7	7:99902175	TTTTTATTTTAGTTG[C/T]TGCAGACAAGAAAAC	89122
rs372246449	snp	C/T	1.6599e-05	0.00288084	missense	TRIM4	GRCh38.p7	7:99903299	CAAGAGAATAGTTCA[C/T]ATCCTGGATCTCACT	89122
rs372374118	snp	C/T	1.64882e-05	0.00287121	missense	TRIM4	GRCh38.p7	7:99892279	GGTGCACTCCGTCCA[C/T]AGCGCTGTAGAAGGA	89122
rs372624872	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99897598	ACAAAAGATTTCTCA[A/G]GTCGGTTCTTGCACT	89122
rs372638521	snp	A/G			missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919305	GGTGCAGGCAGCCGC[A/G]GCAGAAGTTGTGGCC	89122
rs372808047	snp	A/G	8.65539e-05	0.00657795	intron-variant	TRIM4	GRCh38.p7	7:99908569	AGATCACCCCCACTC[A/G]TAACTGTCTCACCTG	89122
rs372949570	snp	A/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918566	TGAGACTCCATCTCA[A/G]AAAAAAAAAAAAAAT	89122
rs372978358	snp	C/T	0.000103003	0.0071757	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919433	GGAGACGGAGTCCGA[C/T]GTGAGGCGCGGGAGA	89122
rs373018289	snp	A/C/T	4.97404e-05	0.0049868	missense	TRIM4	GRCh38.p7	7:99909630	TCTTCATCTTGGCCA[A/C/T]GAGATTACGCTGAGA	89122
rs373106721	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99901105	TAAAGTTGTCCCACA[A/G]GTCACTGATGCTCTT	89122
rs373119343	snp	G/T	1.75903e-05	0.00296561	intron-variant	TRIM4	GRCh38.p7	7:99908555	AGTTAGTGAAGATGA[G/T]ATCACCCCCACTCGT	89122
rs373409531	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918422	AAACAAAAATTAACC[A/G]GGTGTGGTGGCGTGT	89122
rs373474956	snp	C/T	1.65578e-05	0.00287726	missense	TRIM4	GRCh38.p7	7:99892233	AAAAATGGCCGGAGG[C/T]GTGAGACAGAAGAAC	89122
rs373581152	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99897298	TCCACCTGAAAGAAG[G/T]CAGACCACCACAATG	89122
rs373686349	snp	G/T	0.000153988	0.00877328	synonymous-codon	TRIM4	GRCh38.p7	7:99903306	ATAGTTCACATCCTG[G/T]ATCTCACTCCTAAGA	89122
rs373703372	snp	A/G	3.61298e-05	0.00425013	intron-variant	TRIM4	GRCh38.p7	7:99902140	GTTGTTTCACATATT[A/G]TGCCTGTTTTGTTTT	89122
rs373721214	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99913625	GCAGTGAGCTGGGAT[C/T]GCGCCACTGCACTCC	89122
rs373750692	snp	A/G	3.30431e-05	0.00406454	intron-variant	TRIM4	GRCh38.p7	7:99916812	ATCATATCATTCCCT[A/G]CCTTAAAACCCTTTT	89122
rs374082358	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99917176	AAATACTTCAGCTAC[C/T]CTCACACACACTGAA	89122
rs374083501	snp	A/C			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918845	CATTCCAGTTTTAAC[A/C]CTAGCTCTGAAATTC	89122
rs374182247	snp	A/G	0.00597247	0.0543191	intron-variant	TRIM4	GRCh38.p7	7:99904790	TAATCCCAGCACTTT[A/G]GGAGGCTTAGGTGGG	89122
rs374262278	snp	C/T	0.000971473	0.022018	missense	TRIM4	GRCh38.p7	7:99908688	GTGTTCTCATTCAGC[C/T]TCTTCTTCGTCTCTT	89122
rs374362576	snp	C/T	6.59794e-05	0.00574329	intron-variant	TRIM4	GRCh38.p7	7:99903630	GACATAAGCAAATTA[C/T]GAACCTTCTCCTGGA	89122
rs374510134	in-del	-/TG			intron-variant	TRIM4	GRCh38.p7	7:99896041	TAGTATGATTAGATT[-/TG]TGTCTATTATTTTGC	89122
rs374536807	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99912955	CCCTGCTACTCTCTC[A/T]TGTAATTTCACTTTA	89122
rs374955547	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99895490	ATCTTGGAAAATGTT[C/T]CACGTACACTGAAAA	89122
rs374963870	snp	A/G	4.94597e-05	0.00497266	synonymous-codon	TRIM4	GRCh38.p7	7:99892283	CACTCCGTCCACAGC[A/G]CTGTAGAAGGAGACA	89122
rs374965082	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905793	ATCTCACAAACGTAA[C/T]GTGAGCAAAAGAAGC	89122
rs375065820	snp	C/T	4.94597e-05	0.00497266	missense	TRIM4	GRCh38.p7	7:99892282	GCACTCCGTCCACAG[C/T]GCTGTAGAAGGAGAC	89122
rs375223839	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99898566	GCCGGACACATTCTG[G/T]CCCATTGAGACACCA	89122
rs375225704	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99894671	GACTCCATCCCCCCC[C/T]CAAAAAAAAAAAGAA	89122
rs375295210	snp	A/G	1.6477e-05	0.00287024	missense	TRIM4	GRCh38.p7	7:99892368	TGGGTGGGAGTTCCA[A/G]GGAAGCCTATCAAGG	89122
rs375475849	snp	C/T	1.64817e-05	0.00287064	intron-variant	TRIM4	GRCh38.p7	7:99903538	CCTGTATCTTTACCA[C/T]GCCACCCAGGTCCCC	89122
rs375527938	snp	A/G/T	0.000120257	0.00775334	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919443	TCCGACGTGAGGCGC[A/G/T]GGAGAGGCCAGCAAG	89122
rs375761581	in-del	-/CA			intron-variant	TRIM4	GRCh38.p7	7:99894672	ACTCCATCCCCCCCC[-/CA]AAAAAAAAAAGAAAA	89122
rs375776910	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99895478	CCAGCTTAGTCTATC[C/T]TGGAAAATGTTTCAC	89122
rs375931857	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99914172	GCCCTCCCTACTTAC[A/C]GTCATGTCCTTCTCT	89122
rs375945745	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906918	CACTGCAGCATTATT[C/T]GTAGTGGTAATGGTG	89122
rs376124922	snp	C/T	0.000387855	0.0139204	intron-variant	TRIM4	GRCh38.p7	7:99916795	CTAAAACAAAAAAAA[C/T]GATCATATCATTCCC	89122
rs376192236	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911634	AAGTTAAATAACTGA[C/T]AAGGTTGATAACATC	89122
rs376233157	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99895205	AGCACTATACACTTT[C/T]CTTTAAGTTTTGCTT	89122
rs376234532	snp	A/C/G	3.32227e-05	0.00407559	missense	TRIM4	GRCh38.p7	7:99909639	TGGCCACGAGATTAC[A/C/G]CTGAGACTTAAGAAG	89122
rs376427270	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920093	ATGCTCACCTGTTTC[A/G]GGGAATTATCTATAT	89122
rs376720616	snp	C/T	4.9525e-05	0.00497595	missense	TRIM4	GRCh38.p7	7:99908789	CTCCGTGCTGATTCT[C/T]ATTCGCTGACTCTTT	89122
rs376793435	snp	C/G	1.65971e-05	0.00288067	synonymous-codon	TRIM4	GRCh38.p7	7:99909577	TACCTTCCACTGTGT[C/G]GCGTTCTTCACTTCT	89122
rs376896164	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99917288	TGTTTGGCAAATAGT[A/T]AGCATCAATAAACGT	89122
rs376972342	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99908527	ATTCAGCTCTAAAGA[C/T]AAGAGAGAGTTCAGT	89122
rs377019955	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99912581	ATCTGGTTAATGATA[C/T]ACATGCTGAAGTATT	89122
rs377119923	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99898490	AGGTAGACGGCAACC[A/G]CAGCTGGCCTTACTT	89122
rs377177279	snp	A/G	5.68392e-05	0.0053307	stop-gained, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919065	GAGTCTGGTGCTCCT[A/G]GGACTCCCTGCACAC	89122
rs377304266	in-del	-/GGGTTTCTTCATATTTCTC			intron-variant	TRIM4	GRCh38.p7	7:99900932	TCTTCATATTTCTCA[-/GGGTTTCTTCATATTTCTC]TACTCAGGGTTTGTT	89122
rs377336090	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902477	GTCTCGAACTCCTGA[C/T]CTCAAATGATCCGCC	89122
rs377376905	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920942	ACCTAAGTATTGAAT[A/G]AGAAGTTTCAGCATT	89122
rs377457227	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99894270	GTAATACAGGCCTCA[A/C]AGAAAGAATTGGGAA	89122
rs377523897	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896563	CTATGTCTCATTCAC[C/T]GGCTCCAGGTTTCTT	89122
rs377540227	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99894509	TCTACTAAAAAAAAA[-/A]TACAAAAATTAGCCA	89122
rs377553249	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99910851	TAGGATGTCAGCTGC[A/G]AGTGCAGAGATGGAA	89122
rs377580456	snp	C/T	0.000125638	0.00792486	intron-variant	TRIM4	GRCh38.p7	7:99902087	ATTTCTCAGGAATCA[C/T]CGTCCTTCACTGCCT	89122
rs377701784	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904158	TTAAGCCATGAAATG[A/G]AACAGTAGAAAAAAA	89122
rs377709959	snp	C/T	1.65004e-05	0.00287227	intron-variant	TRIM4	GRCh38.p7	7:99903638	CAAATTACGAACCTT[C/T]TCCTGGAGACCTGGA	89122
rs397791409	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99900715	TGAAGGATATTTTTT[-/T]GCCAGTTCTAGAACT	89122
rs397974281	in-del	-/A			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918580	GAAAAAAAAAAAAAA[-/A]TCTCATTGATAATTT	89122
rs398005571	in-del	-/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99905062	TCCTTGATAAAGCTA[-/T]TTTTTTTTTTTAATT	89122
rs527311351	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893125	CAAAAAAACTGGCCC[A/G]GCATGATGGTGGGCA	89122
rs527362351	snp	C/T	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892492	ACACCCCAACAGCAA[C/T]CTCCAGACTATCTCT	89122
rs527492074	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900901	CCAGCAAGTTATGAT[A/G]AGCCTTGGCATATTT	89122
rs527621849	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99907079	ACAGTAGTTCTCTCA[C/G]GCTCTGAGATTCTAT	89122
rs527794525	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891733	GTAACCAAATACAAC[C/T]AAAATTGTCTTATAC	89122
rs527965753	snp	A/C	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99914086	AATCTACCTACATGC[A/C]AAACCCCACTGCCAC	89122
rs527967373	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905883	GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	89122
rs528118434	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904134	CAGAGACTATTATAA[A/C]CTTGTTCCTTAAGCC	89122
rs528154903	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911931	TGGCAAAAACCGCAA[C/T]TACATTTGCACCAAC	89122
rs528193906	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918890	TTCTTTGAGTTTCAG[G/T]GGCTTTTCATGCTTC	89122
rs528389863	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99904836	CAGGAGTTCAAGACC[A/G]GCCTGGCCAACATGA	89122
rs528436247	in-del	-/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99901495	AGGTGCTCTTTTTTT[-/G]TTTATTTCTACCAAT	89122
rs528523536	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896338	TTTCTAGGAAGGACA[C/T]CTGAACATCTGAACC	89122
rs528616947	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902386	CCGAGTAGCTGGGAT[G/T]ACAGGTGCACACCAC	89122
rs528643720	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918358	GATCACTTGAGGTCA[A/G]CAGTTCGAGACCAGC	89122
rs528705765	snp	A/G/T			intron-variant	TRIM4	GRCh38.p7	7:99896731	GGCTGGTTGTCCACA[A/G/T]GTATGTGGGGCCCAA	89122
rs528724668	in-del	-/A	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99893194	ATCACTTAAACCCAG[-/A]AGGCGGAGGTTGTAG	89122
rs528809824	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99889966	TTCACGTTGTTTCCA[C/T]CTGGCATTTTTCTGT	89122
rs528828673	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99895159	GTGGAAGCTGAGGTC[A/G]GTGATTTGAGAAGTT	89122
rs528845380	in-del	-/AAAG	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99894691	AAAAAAAAGAAAAGA[-/AAAG]AAAGAAAAGAAACAA	89122
rs528855585	in-del	-/TA			intron-variant	TRIM4	GRCh38.p7	7:99904681	AATTGTTCATTTTTT[-/TA]AAAAAACTGGTTAAT	89122
rs528992914	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99912648	ATAAGAATTGATGTA[C/T]TCAGAGAGATACAGA	89122
rs529116359	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891772	CGTAATTATCTCATA[C/T]AACAAGAAGCTTGGC	89122
rs529117564	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99911330	GGTGAAAAACCAAGA[C/G]AGAATGGTTTCTCCT	89122
rs529151516	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99898702	TACCTGTGCCATGCC[A/G]TTACTCTTCTCACTG	89122
rs529237537	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99907299	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	89122
rs529336417	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890034	TTTCCTTCTTTTTAT[A/G]AGGACACCAGTCATA	89122
rs529471876	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919526	CACGTAAAAGGGTAC[A/G]ACGCAGTTTCTCTTC	89122
rs529722079	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901657	GAGGCAAGATTTTCC[C/T]GAGTACGCTACTCAG	89122
rs529744043	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99900374	TGACTTAAATGTTAA[A/T]CTTATCCAAAATCAC	89122
rs529886676	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903108	ATTAACCACCTTTCC[C/T]GACACTCTATTAGCT	89122
rs529960174	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918081	TAGTAACAAAACCCA[C/G]CCTCATCATTACAAG	89122
rs530079849	snp	A/C/T	5.07398e-05	0.00503664	intron-variant	TRIM4	GRCh38.p7	7:99908840	GAGATTTGCTCACTC[A/C/T]TTTTTCTGCCTGACC	89122
rs530189819	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908222	AGTGTCTCTTAATTG[C/T]TGATAACAGTTATGT	89122
rs530333112	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901583	TGGGTCTTGCTTTCA[C/T]GATTTGTAAGGTGGG	89122
rs530333197	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893892	TTGAGGACTTTTTTT[A/T]AAAAAAATCAGGAAT	89122
rs530451054	snp	A/G	0.00557542	0.0525036	intron-variant	TRIM4	GRCh38.p7	7:99902631	CCTTGGTGCCTCCCT[A/G]GAGATCCAATGAGTT	89122
rs530511093	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918217	TTCCAAACTGCTATG[C/T]GTTGTAAATGTAAAA	89122
rs530548296	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99917636	AGGCAGGAGAATCAC[C/T]TGAACCCGGGAGGTG	89122
rs530737141	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911830	CATAAATAGACCTGT[A/G]CAAGAATATTCATCG	89122
rs530858499	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99902321	GATACAATCTCAGCT[C/T]ACTGCAACCTCCACC	89122
rs530861593	snp	A/C	0.0667028	0.170006	intron-variant	TRIM4	GRCh38.p7	7:99894672	ACTCCATCCCCCCCC[A/C]AAAAAAAAAAAGAAA	89122
rs531081329	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99895007	TTACTGAAATTCTCA[A/G]AGGACCAGCTTTTGG	89122
rs531220503	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99894042	ACTATGCTCTTCTGG[C/G]ATAAATCTCACATAT	89122
rs531398709	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893701	ATAGCTAGTTAGTCA[C/T]CAAGTCCTACCAATT	89122
rs531437380	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893176	GGAGGCTGAGGCAGA[A/C]GAATCACTTAAACCC	89122
rs531484110	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916544	CTGACAGTCATCTAC[C/T]TGCCATCTGAAGCAG	89122
rs531486074	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99906607	TTTACCAGCAAACAA[A/T]GGGGTAAATATAAAG	89122
rs531550150	snp	C/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917971	GCAGAGTAAGGTAAA[C/G]TGATTTATTCAACCG	89122
rs531635684	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915706	GGATGGAGAGATGGG[C/T]GGATATCAGGGAATT	89122
rs531680673	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920892	TTACTGATGTTTACC[A/G]TGAGTGTTTATGGCA	89122
rs531897299	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899611	TCTCCTCTCCCAATC[C/T]TCACACTACTGTCAT	89122
rs531935222	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99906687	CCCAAGGACCAATTT[A/T]AAAAAAAACAGCTGG	89122
rs531972348	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900217	AAGGCCATTAGGCAG[A/G]AAGAGCCAATGCTGC	89122
rs532007893	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907301	TTTTAGTAGAGACGG[A/G]GTTTCACCATGTTGG	89122
rs532098198	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99905236	ACAGCAACTGGAACT[C/G]TTAATTTTACACACT	89122
rs532114950	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99894628	GCTGAGATTGCACCA[C/T]TGCGCCCCAGCCTAG	89122
rs532302474	snp	A/T	1.74805e-05	0.00295634	intron-variant	TRIM4	GRCh38.p7	7:99909688	ACACACACAGGTAAG[A/T]AAACACATCTCCAAC	89122
rs532332071	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907378	ACCTCCCAAAGTGTT[A/G]GGATTACAGGCGTGA	89122
rs532362139	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915316	CAAAGCCAGTGCTCA[A/G]TAAACATCTTAAATT	89122
rs532423787	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99899722	GAACAGAACCAAAAG[G/T]ATATATATGTCTGTG	89122
rs532465882	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914679	ACATATCCAGCTCTC[C/T]CCCGCCTCAGGGCCT	89122
rs532713700	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99900253	AGGCCAAGGTAGTAT[A/G]CTTTAGAAATCCATC	89122
rs532784850	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893854	CAAATTCCCTTCCCT[C/G]TAACTCTCCATGTCT	89122
rs532838102	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891860	TCCACCATTCCTGTG[C/T]TCTCAGTTCCAATAT	89122
rs532869534	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898913	GAAAAGCTTTCTGTA[C/G]AGTATGATTGCTACT	89122
rs532992592	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899411	GACTGCCCTGCATGT[A/G]GGTCTTCAATAAACC	89122
rs533045952	snp	A/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99906313	TGGTCACTTTGTGAT[A/T]ATCTGTCAAGCTTAT	89122
rs533068290	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99913495	AACATGGTGAAACCC[C/T]GTCTTTACTAAAAAT	89122
rs533081115	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905824	CAGTACGAAAGAGTG[C/T]GTCCTGAAAGATACT	89122
rs533112875	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99914520	AAGATTCTTCACTGG[C/T]TTTCCTCTTCACCAA	89122
rs533438018	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890987	TTTTATACTTTTTGC[A/G]TCTTACAAACTTTCT	89122
rs533476321	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898035	AGAGTTGCCCCTCTC[C/T]TCCACAATGGGCCTG	89122
rs533485564	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919596	GGCCTGAGCGCGCAA[A/G]ACCGGAAGCTGCTGG	89122
rs533524384	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913522	AAATACAAAAAAAAA[A/T]TAGCCGGGCATGGTG	89122
rs533664253	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912787	TTTCATGGTAAAATG[A/G]AATAGGAAAACAAAA	89122
rs533668120	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920077	GCTTTCAACAAATAA[C/T]ATGCTCACCTGTTTC	89122
rs533869806	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913753	ACCAGAAAATTATAC[A/G]TATATGAAAACACAA	89122
rs533892832	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891976	TCCCATCTCCATTGG[C/T]CAGACCCACCTCCCA	89122
rs533940509	snp	A/T	0.0023933	0.0345097	intron-variant	TRIM4	GRCh38.p7	7:99906873	AAATAAAAATAAAGA[A/T]AAACAATAAAGAGCA	89122
rs534024815	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99912356	GGCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA	89122
rs534067962	snp	A/C	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919222	CCAGTTGGGTCGCAG[A/C]GCGGCGGGCGCCGAT	89122
rs534133682	snp	C/G	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99904500	AATACTAGGTAAAAA[C/G]TGAGGAAATGGAAAT	89122
rs534171565	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891353	TGATGAGAGTCATAT[G/T]CAACAGCATATGAAG	89122
rs534272019	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905030	AGCGAGACGCTGTCT[A/G]AAAAATAAAAAATAA	89122
rs534297345	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919715	GAGACCCAGAAATGC[C/T]TGTGGAAAGCTACAG	89122
rs534844166	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910023	AGCCATGAGCCACCA[C/T]GCCTGGCAACTTCAT	89122
rs535003002	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917732	CTCAAAAACAATAAT[A/C]ATAAAATAAATAAAT	89122
rs535154974	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897189	ACTGGGATGAGTCCA[C/T]AGAGGTTCCCATCCT	89122
rs535235868	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919772	GACGTTGTGGTCCCT[C/G]GGGGAGCCAACCGGG	89122
rs535321010	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906234	GTACTGATTGGGGAC[A/G]TGAGGAAGCTTCTAG	89122
rs535824192	snp	C/T	0.0134861	0.0810011	intron-variant	TRIM4	GRCh38.p7	7:99909161	GTGTGTGTGTGTGCG[C/T]GTGTGTGTGCATCCA	89122
rs535966554	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99911856	CATCGCAGCTTTATT[C/T]ACAATAGCTAGAAGC	89122
rs535972880	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99897678	ATCCTACTCCCCAAC[A/C]CCCTGTATTTCCAAA	89122
rs535979330	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99893368	TATTAACAAATTCTC[-/AT]ACGTTGAATCAAAAC	89122
rs536180667	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918379	CGAGACCAGCCTGGC[A/C]AAGATGGTGAAACCC	89122
rs536183163	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910377	AATATGTAAAGAAAT[A/G]GTCACTATAGCATTA	89122
rs536285203	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893455	TAGGACAGAATAATG[A/T]GGTCTCTTTTCACGG	89122
rs536322131	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99892911	AGCAGGCCACAGCAT[A/G]GCCTTTAGCAACCTG	89122
rs536332903	snp	C/T	1.65244e-05	0.00287436	missense	TRIM4	GRCh38.p7	7:99908613	GTGGGAGCCTGGCTC[C/T]TCTCCCCCACCTCTA	89122
rs536360671	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899763	GTGGGTGGGTGTGTG[G/T]GCGCACACGTGCATG	89122
rs536384752	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99894998	GTGTCAATTTTACTG[A/T]AATTCTCAAAGGACC	89122
rs536528779	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895132	TTGCTCCTCTTTCTC[C/T]AGTGTCTTAAGGTGG	89122
rs536563569	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901867	ATAGATGGCGAGGGT[C/T]CTCTCTGTGTCCGGC	89122
rs536653239	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902406	GTGCACACCACTATG[C/T]TCAGCTAATTTTTGT	89122
rs536784427	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909198	TGTTTCTTTCCACAA[C/T]GCCATGGGCCCAAAC	89122
rs536969590	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895710	TTTTGCTTAATATGT[G/T]TGAAGCACTGTTAAG	89122
rs537009123	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895189	TTCTTCTTTCCAATA[C/T]AGCACTATACACTTT	89122
rs537034924	snp	A/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920014	CCTTTTTGGTATCCA[A/T]TTTGAAAAGTAGCAA	89122
rs537047269	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99916860	GAAAGAGAAAGTTCA[A/T]TCTTTTTACTATGGC	89122
rs537133131	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894048	CTCTTCTGGGATAAA[C/T]CTCACATATTGTGAT	89122
rs537146193	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902042	CAGGCAGAGGGTAGG[A/G]CAATCATAGGCTGAC	89122
rs537171945	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893529	TCATTCAAAACTGAA[A/C]TAATTATCTTACTTA	89122
rs537255305	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916178	ATACCCATCCACTTA[G/T]ATTTCCCTCGGCCCC	89122
rs537339110	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896603	AGACACAGTGCCATC[C/T]GTACTGAAATCAATA	89122
rs537747194	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99895653	CTGAAAACTGCAAAC[A/G]TAATTGTGAATTTGT	89122
rs537785697	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907058	TGGGTAGGTAGATAG[A/G]TAAGTACAGTAGTTC	89122
rs537810336	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898482	ATGGCTACAGGTAGA[C/T]GGCAACCACAGCTGG	89122
rs537813570	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914440	GGATTATAGGCATAA[A/G]CCACCACACCTGGCC	89122
rs537843209	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921410	TGCCCCATCCCAACA[A/G]GGTGAACCAGCTGAT	89122
rs537952778	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99905379	CAGGTATACAACTGA[C/T]AGAAATGTATATAAA	89122
rs538007231	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900410	AAAAAACACCCAAAA[C/T]AATTTTTGACCAATA	89122
rs538178285	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914964	ACAGGTGCCCACCGC[C/T]GCACCTAGCTGATTT	89122
rs538200725	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99905929	GCAGGCGGATCACTC[A/G]AGGTCAGGAGTTCAA	89122
rs538523116	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892064	GACCCAGAAGATGGA[C/T]CATCCAGGATAGAGA	89122
rs538594150	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907727	GATAATAACTACTGG[A/G]TGGGTCCAGGTTTCT	89122
rs538641461	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99895443	ATCGGAATCCTTTGA[A/T]TTTGACACTTGCTTT	89122
rs538646374	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99898632	TTCCAGAAGTGTGCA[C/T]TCTGGAGTTGCAATT	89122
rs538720470	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99915007	TAAAGACAGGGTTTC[A/C]CCATGTTGGCCAGGC	89122
rs538741490	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906774	TTACTTGAGCCCAGC[A/G]GCTTGAGGGTGCAGT	89122
rs538780813	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914259	AACTCCTGAGTGCAA[C/G]TGATCCTCTAGTCTC	89122
rs538983112	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899693	AAATAGTCAATTATT[A/G]GGGTTCTCCAAAGGA	89122
rs539166716	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890658	CTCACGTATAAGGGA[C/G]AGCTAAACATTGAGT	89122
rs539215762	snp	A/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99913713	AATAATAATTTTTTT[A/T]AAAATCACTTTCTCT	89122
rs539384229	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919811	TATGATCTTTCTTTC[C/T]AAGTTTGAGGGTTCA	89122
rs539486473	snp	C/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919837	GTTCAGGTCTGTGTT[C/T]GCCTGCTGGTTAGAC	89122
rs539603499	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897234	TGGTCACTACCAAGA[C/T]AAAAGAAGACCAACC	89122
rs539625383	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920422	CATTTGCCTTATTGG[G/T]GCATGGTCTGATCAG	89122
rs539770825	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99916382	TGAGGATTCTAAAAT[A/G]TTATCTCTAGCCTCC	89122
rs539787680	snp	A/G	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919141	CTCCCAGTGGCGGCC[A/G]CACAGGCCCGGGGGC	89122
rs539812426	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911206	GTGAGCGTAAAATCA[C/T]CCAGTAAGATTCTAT	89122
rs539846666	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918492	ACTGCTTGAACCCCG[C/G]AGGAGGAGGTTGCAG	89122
rs539848809	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912626	ATTTTAAAAGCATCA[A/G]AAGGAAATAAGAATT	89122
rs539988636	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899269	GCAATACAGGGAATC[A/G]AGGCCCTTTCTTTTG	89122
rs539997585	snp	A/T	0.0146672	0.084371	intron-variant	TRIM4	GRCh38.p7	7:99905043	CTAAAAAATAAAAAA[A/T]AAAAATTAAAAAAAA	89122
rs540004128	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919474	CTGCGAGCGGCCGCG[A/G]GGAGGCCAGACGACT	89122
rs540147175	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99906130	AGCCTCGGCCACACA[A/G]CAAGACTCCATCTCA	89122
rs540162146	snp	A/G	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99905687	AAATGTCTCTATATA[A/G]TATCAGATTTTGCCC	89122
rs540234433	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919908	CAGCCTAGGGGCCTG[A/G]AAGGCCAGGAAGACT	89122
rs540459499	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902689	TCTCAACCTCAACCT[C/T]TACCTTTCCTCAAAA	89122
rs540583618	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99889984	GGCATTTTTCTGTGT[A/G]TGTGTGGGCATGAGT	89122
rs540720193	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903653	CTCCTGGAGACCTGG[A/C]ATACAACTGTGTGAG	89122
rs540758849	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902993	CTCCAATGTGCTTAC[A/G]AACTCATGAAGAAGT	89122
rs540788463	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895361	TTGATATTTAGGGGG[G/T]TTTCTAAGGATATTT	89122
rs540822778	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899746	GTCTGTGTCTGTGTA[C/T]GGTGGGTGGGTGTGT	89122
rs540833517	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910570	GTGTCTATGCGCATA[C/T]GTGTTTATCTATGTG	89122
rs540878831	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918000	CGGAGCTTCTTAACC[A/C]ATGAGATAGGACAGA	89122
rs540900616	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99904510	AAAAACTGAGGAAAT[G/T]GAAATAAACTACAAA	89122
rs540909291	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99899805	GAGTTTTCTGGGTTT[A/T]CTTTTGAGATGGGGT	89122
rs540915481	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99914275	TGATCCTCTAGTCTC[A/G]GCCTCCCGAATAGCT	89122
rs541181603	snp	G/T	1.94759e-05	0.00312051	intron-variant	TRIM4	GRCh38.p7	7:99902173	TGTTTTTATTTTAGT[G/T]GCTGCAGACAAGAAA	89122
rs541193006	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918522	GTGAGCCAAGATCAC[A/G]CCACTGTGCTCCAGC	89122
rs541207143	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99917146	CTCCGACCTCAGACC[C/T]TCTGTACACTTGGTA	89122
rs541316978	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909360	TCCTCTCCTATCCCC[A/G]TATCTACAAGGGGCC	89122
rs541318911	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901533	GGCTTTATCCTGGGA[C/T]GCAGTTAAGTTAGTT	89122
rs541353597	snp	A/G	0.000197674	0.00993972	synonymous-codon	TRIM4	GRCh38.p7	7:99908735	TCTCTGAAGAAACAG[A/G]TCCTCTTCTTCAACC	89122
rs541402821	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99893760	TTTTCCTCCCCTCCA[C/G]TCCCATTGCCACTGC	89122
rs541404242	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918093	CCAGCCTCATCATTA[C/T]AAGCTAGGCTTTTCC	89122
rs541410712	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906001	AATAGAAAAATTAGC[C/T]AGGTGTGGTGGCACA	89122
rs541417484	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99915345	TTAATTAACAGAATG[C/G]AGGGATTAGCTCCTA	89122
rs541569862	snp	A/C	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99894637	GCACCACTGCGCCCC[A/C]GCCTAGGCAACAGAC	89122
rs541632671	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99903708	TGCTCATGTCACATA[G/T]GATCTCCTGCTGCCA	89122
rs541645504	in-del	-/TT			intron-variant	TRIM4	GRCh38.p7	7:99909749	TTTTTTTTTTTTTTT[-/TT]GAGACAAAGTCTCAC	89122
rs541669031	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99911808	TGGAAAAATGAAAAC[A/G]TGTACCCATAAATAG	89122
rs541772398	in-del	-/TC	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99907199	CTCGGCTCACTGCAA[-/TC]TCTGTCTCCCGGGTT	89122
rs541832124	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909483	TGCAAAACCCCATGA[C/G]CAAAAGGACCTCAGA	89122
rs541900988	in-del	-/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99907299	ATTTTTAGTAGAGAC[-/G]GGGTTTCACCATGTT	89122
rs541979917	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896166	AGCTACATCTCTTTT[A/G]TTTTAGTGGTTTAAG	89122
rs542384323	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907792	TGCTTATGAAAAAAA[A/T]ATAGTAATGGTAGAC	89122
rs542420422	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99893624	CTAAGGTGTCAGAGT[A/C]CCCTCCACCTGAACA	89122
rs542588395	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920814	TTTGCAAATTGGAAT[A/G]CTCTATGGAGAAGGG	89122
rs542598033	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893662	TTTTAAATCTTTATT[C/T]TCGACTCTTTCCTCT	89122
rs543115417	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99899112	CAGCAGTAACTCCAG[C/G]ACACCCTGAGAATAA	89122
rs543180536	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907244	TGCCTCAGCCTCCCA[A/C]GTAGCTGAGATTACA	89122
rs543217701	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914590	CCGCTGCCTACATCT[C/T]GTTTCACATCGCATG	89122
rs543226741	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99896537	CCCAGCATATAAGTC[C/G]TCAATAAATCCTATG	89122
rs543370717	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892103	GCAGAAGAGGGCCCA[A/G]GGATGTGTGTCCCTC	89122
rs543395551	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921255	GGAACCTAAGACACG[A/G]GCTGGTCATTCTTTC	89122
rs543454836	snp	A/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918207	AACGTGGATATTCCA[A/T]ACTGCTATGTGTTGT	89122
rs543581335	snp	A/G	3.29489e-05	0.00405874	missense	TRIM4	GRCh38.p7	7:99908673	TGATTGAGTTTTAAC[A/G]TGTTCTCATTCAGCT	89122
rs543611500	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99917363	GTCTGTTTCCTGTTC[A/C]TAGTCAGCTGGTACA	89122
rs543751374	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915208	CCCACCCTCAGCCCA[A/G]CTGGACTGTGAGCTC	89122
rs543764546	snp	A/G	0.00795532	0.062565	intron-variant	TRIM4	GRCh38.p7	7:99896703	CAGGGGAGAATCCAC[A/G]GTGGAAATCCTGGGC	89122
rs543874400	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905815	AAAAGAAGCCAGTAC[A/G]AAAGAGTGCGTCCTG	89122
rs543967699	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99900725	TTTTTTGCCAGTTCT[A/G]GAACTCTAGGTTAAC	89122
rs544095744	snp	A/G	6.59185e-05	0.00574064	missense	TRIM4	GRCh38.p7	7:99892312	CATTCCCAGTCCCAC[A/G]ATCCAGGTAAACCCC	89122
rs544363252	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920641	TTTTATGTCCCAATA[C/T]CAAATACTGCCTTTC	89122
rs544369077	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913428	AATCCCAGCACTTTG[A/G]GAGGCCAAGGCGGGC	89122
rs544471541	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902847	AAATCTCAAAACTGT[C/T]GCCTCTGCTGTGAAA	89122
rs544527654	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899319	GGTGGAGATTGCTAA[A/G]TGAAAATGCTATATA	89122
rs544718063	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897918	CTTGTACCCACTAAA[C/T]ATCTCACCTGTTGCC	89122
rs544974341	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900067	TTGGGATTACAGATG[G/T]GAGCCACCACACCCA	89122
rs545014116	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99908213	AGAAAGTTAAGTGTC[-/T]CTTAATTGTTGATAA	89122
rs545033661	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892132	TCAGCTGGACTACAG[C/G]GAAGGAGTTTTGGTC	89122
rs545116295	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907189	GTGGCACAATCTCGG[C/T]TCACTGCAATCTCTG	89122
rs545137440	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99894548	GGCGCGCACCTGCAG[C/T]CCCAGCTACTTGGGA	89122
rs545153119	snp	A/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99906371	CATACTTTTTTTTTT[A/T]AAATAGAGACAAGAT	89122
rs545178691	snp	G/T			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890335	TGTAAGAATCCTCAC[G/T]ACCACCATTCAACCC	89122
rs545361593	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99911845	ACAAGAATATTCATC[A/G]CAGCTTTATTCACAA	89122
rs545424439	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920085	CAAATAATATGCTCA[C/T]CTGTTTCAGGGAATT	89122
rs545463220	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891642	TTTGTCAAATTTCAC[A/G]AAAGTGACTTAAGCC	89122
rs545481671	in-del	-/GTTTA	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99909101	TAGCCTTCAGAACTC[-/GTTTA]GTTTTACCAAATCTT	89122
rs545489747	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918851	AGTTTTAACCCTAGC[C/T]CTGAAATTCGTGTTT	89122
rs545593441	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920678	TAATTTTTCTCAGTA[A/G]GTAGTATGATTAAAT	89122
rs545602483	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99905345	CACATGTATGTCCTA[C/T]GACCAGGAATTGTTC	89122
rs545634822	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898044	CCTCTCCTCCACAAT[A/G]GGCCTGCCATGGGGC	89122
rs545686470	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904758	TTTATCTGGATGAGT[A/C]CAGTGGCTCATGCCT	89122
rs545753250	snp	C/G	0.000114345	0.00756037	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919317	CGCGGCAGAAGTTGT[C/G]GCCGCACTCGATGGA	89122
rs545846978	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99906166	AAAAGTAAAAAAAAA[-/G]TTAGAGTGTGAGAAG	89122
rs546152143	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904884	TAAAACTACAAAAAT[C/T]AGACAGGCATGATGG	89122
rs546186081	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902336	CACTGCAACCTCCAC[C/T]TCCCAGGTTCAAGCG	89122
rs546225428	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99910478	GCTGTCTATATATTG[A/G]CATGAAATACACAAT	89122
rs546317952	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901892	TCCGGCTCTCTCCGC[C/T]CCAGGATACTGCCCA	89122
rs546473407	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896822	CAAAAGTTCTGGAAG[A/G]ACTGCTGCAGGGGGT	89122
rs546516962	snp	A/C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898119	GCATGATAAGTCTCA[A/C/T]CCACTTCCCTTCAGC	89122
rs546553401	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895316	TCTTCTTTAATTCAA[A/G]GGTTACTAAAAAGTC	89122
rs546612219	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890447	CAGCACTATTCACAA[C/T]AGCAAAGACATGGAA	89122
rs546862977	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891119	AGCAGAAGGGTAGAC[G/T]GAGGAAAATATACAC	89122
rs547057308	in-del	-/TC	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99914805	CACTTTTTCTTTTTT[-/TC]TTTTTTTCTTTTTTT	89122
rs547103691	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896359	CATCTGAACCTCTGG[C/T]CCATTCTTGGAATGC	89122
rs547144308	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895575	TTGATTGATAATATT[A/T]TTCAAGTCTACTATA	89122
rs547146260	snp	A/G	0.00188501	0.0306423	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918995	CGTCATAGTCACCGC[A/G]ACGGCCAGCTCACCC	89122
rs547350403	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900295	GCCTTTTTTTTCTAT[C/T]CAAGCCTTCAACTGA	89122
rs547352253	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908020	GTAAAGATTAACTCA[A/G]AGGAGGGGCTTTTGA	89122
rs547523192	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906796	GGGTGCAGTGAGCTA[C/T]GAGCACACCACCGCA	89122
rs547570227	snp	C/T	1.834e-05	0.00302815	intron-variant	TRIM4	GRCh38.p7	7:99909700	AAGAAAACACATCTC[C/T]AACCATCATCATCTT	89122
rs547577422	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902401	TACAGGTGCACACCA[A/C]TATGCTCAGCTAATT	89122
rs547615365	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901733	ACTGTTCCTGGCCCT[A/G]TGTGAGCACCAGGAA	89122
rs547630036	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99911404	GTGTCAAATGCTGGA[C/G]GGTGGCCTGGGCAAC	89122
rs547714806	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99916064	AAAGAATTACAGTAT[A/G]AAAAATGCTTAGAAC	89122
rs547751972	snp	C/T	0.0209421	0.100162	intron-variant	TRIM4	GRCh38.p7	7:99909157	GTGTGTGTGTGTGTG[C/T]GCGTGTGTGTGTGCA	89122
rs547761638	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893858	TTCCCTTCCCTCTAA[A/C]TCTCCATGTCTCTTG	89122
rs547842412	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99900591	CTGGCATTTTCCTTC[G/T]GTCTGAAGGACTTCC	89122
rs547861447	snp	G/T	0.00478085	0.0486577	intron-variant	TRIM4	GRCh38.p7	7:99909736	TTCTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTTG	89122
rs548019377	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921116	CCATCACAAAATGTC[C/T]ATAAGTCTGTATACC	89122
rs548085339	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902848	AATCTCAAAACTGTC[A/G]CCTCTGCTGTGAAAA	89122
rs548096011	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893409	GCTGCCGACTAGCTG[A/G]TTCTTTGGCTAGATA	89122
rs548188715	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99901042	TTCCATCTCCCTCCC[A/C]ACTCCTCTCTTTCAG	89122
rs548441623	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908268	GCTTGCTTTGTTTTA[C/T]TGTTTAATAATTATA	89122
rs548507863	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894658	GGCAACAGACCAAGA[A/C]TCCATCCCCCCCCCA	89122
rs548509638	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910728	TTTGCTTTAATTTCT[A/G]CAAGTGGCATATGCC	89122
rs548537201	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99901606	AAGGTGGGTGTGGAG[C/T]AGCACCCAGTCAAGG	89122
rs548621158	in-del	-/T	0.491936	0.0629843	intron-variant	TRIM4	GRCh38.p7	7:99909730	TCTTTTTTCTTTTTG[-/T]TTTTTTTTTTTTTTT	89122
rs548980815	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920277	ATTGGGCAGCACTCA[A/G]AACCAAAAGAGGTTC	89122
rs549035941	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920128	TAAGTGGATTTTCGA[C/T]CTTGTGTTTCTGAGG	89122
rs549147403	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99907504	CTCACATGTATCTTC[A/G]AGGTTTCAGATTCTA	89122
rs549182425	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99914723	CTCAGATGGCAGACT[C/T]TGCATCCAGCAAGTT	89122
rs549323160	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906556	TTGTCAAAATCTGTG[G/T]AATACAGAGCAATAA	89122
rs549572042	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99899583	GAGAACTGTATCATA[A/G]TATACTTTCATCTCT	89122
rs549608963	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899064	GGCCATTCAAGGGTA[C/T]GCTGGACTGCAGTGT	89122
rs549697538	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905904	AATCCCAGCACTTTG[C/T]GAAGCCAAGGCAGGC	89122
rs549819096	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920951	TTGAATGAGAAGTTT[C/T]AGCATTCCTGCAAAG	89122
rs549905047	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913631	AGCTGGGATCGCGCC[A/G]CTGCACTCCAGCCTG	89122
rs549914144	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901128	ATGCTCTTTGTGTTT[C/T]TGTAAATTGTTTTAT	89122
rs549969743	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908999	TCTGTCTAGTCATTA[C/T]AGTATTCATTCATTC	89122
rs550006285	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908424	TTAATTTCCTTTGAA[C/T]GGTGAATCTTTGGCT	89122
rs550046898	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906923	CAGCATTATTTGTAG[C/T]GGTAATGGTGTTGGA	89122
rs550085637	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918763	TTTCTTTATTATGAG[C/T]TCCCCAAGGGCCAGT	89122
rs550116452	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900231	GGAAGAGCCAATGCT[C/G]CAGTGAAGGCCAAGG	89122
rs550131286	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891234	ACTGGATTTTAATCC[C/G]AACACTGCCATTTAC	89122
rs550131614	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906739	ATCCCCGAACACTTT[C/G]GGAGATCAAGGCAGG	89122
rs550341996	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920383	ATCTAGGTGTCTGCC[G/T]TATTTGACAATGATA	89122
rs550498401	in-del	-/AAAT	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99913671	GTGAGACTCCATCTC[-/AAAT]AAATAAATAAATAAA	89122
rs550556680	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898260	ACACGATGGACAAGG[A/G]TGAGTAACAAGAGTG	89122
rs550640309	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99894547	TGGCGCGCACCTGCA[C/G]TCCCAGCTACTTGGG	89122
rs551182228	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899461	CCAGATCTCCTCTTC[A/G]GCCTTTCAGACACGG	89122
rs551214084	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919542	ACGCAGTTTCTCTTC[C/T]GGGGTTCAGGACCCA	89122
rs551216229	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912090	CGGTGGTTGCCCTGG[C/T]AGGGGAAGGGTGCAG	89122
rs551277402	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896790	ACCAGGTGAGTATGG[A/G]GATACCCCCAAAATG	89122
rs551484717	snp	A/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99898963	GTTGCTGTAGTTTCT[A/T]ACGCTGCTGCAGCAT	89122
rs551507004	snp	A/C	0.00045798	0.0151255	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919169	GGCACGGGGCCCAGG[A/C]GCCGGCGCTGCGTCT	89122
rs551529965	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914274	GTGATCCTCTAGTCT[C/T]GGCCTCCCGAATAGC	89122
rs551576564	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921254	TGGAACCTAAGACAC[A/G]AGCTGGTCATTCTTT	89122
rs551737773	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919697	CTCCTCCAAACAGCT[A/G/T]TAGAGACCCAGAAAT	89122
rs551759944	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910875	GATGGAAGCAGAAAT[A/G]TTAGAGAAACACACA	89122
rs551774982	snp	A/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890083	AAATGACCTTATCTT[A/G]TTTACATCTGCAAAT	89122
rs551970560	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905857	CTCAAAAATAAGCAC[A/C]ACGAGTGCTGGGTGT	89122
rs552005268	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905044	TAAAAAATAAAAAAT[A/T]AAAATTAAAAAAAAA	89122
rs552058150	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919454	GCGCGGGAGAGGCCA[A/G]CAAGCTGCGAGCGGC	89122
rs552083919	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903937	TCCAGCTTTGAGCTT[C/T]CACTCTTCTCCTTCC	89122
rs552135203	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903671	ACAACTGTGTGAGCA[C/G]GTATTTTCTGACGGT	89122
rs552303678	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890243	GCTGCTCAGGCTGAA[C/T]AGGAAGACAAGCCAA	89122
rs552332666	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99911795	TACTCCTAGACCCTG[A/G]AAAAATGAAAACATG	89122
rs552391216	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99901195	TCTGTCTTCAAGTTC[A/C]CCAATTTTTTCTTTT	89122
rs552420380	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901664	GATTTTCCTGAGTAC[A/G]CTACTCAGTGCCCGT	89122
rs552480181	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917677	TGAGTTGAGATCTCA[C/T]CACTGCATTCCAGCC	89122
rs552515940	snp	A/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99895536	AGCTGTTGGGTAGAG[A/T]GTTCTATAAATAATG	89122
rs552560485	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99896704	AGGGGAGAATCCACG[C/G]TGGAAATCCTGGGCT	89122
rs552594257	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99908176	TTTATCAAGCTGTGA[C/T]TGTAATGATTAAAAA	89122
rs552632576	in-del	-/TT			intron-variant	TRIM4	GRCh38.p7	7:99893968	TCACATGGTTTTCCT[-/TT]TTTTTTTTTTTTTTT	89122
rs552662770	in-del	-/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99914107	CACTGCCACCGCTAG[-/T]TTGAAGCCACCATCA	89122
rs552699902	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99903377	AAGACCTCCACTCCC[A/G]GTCAAAGGTTCTTAG	89122
rs552733341	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99893007	TAATCCCAGCACTTT[A/G]GGAGGCTGAGGCAGG	89122
rs552740274	snp	C/T	0.000403796	0.0142033	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919224	AGTTGGGTCGCAGCG[C/T]GGCGGGCGCCGATGG	89122
rs552985552	snp	A/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890014	TGTGTGAACATATGC[A/G]TAAGTTTCCTTCTTT	89122
rs553049346	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920389	GTGTCTGCCTTATTT[A/G]ACAATGATATGATGA	89122
rs553082636	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99917052	GGCCTGAAATACCTT[A/C]TTTCCTACCTCTACT	89122
rs553117729	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99903140	CATGCTGTTTCCTCT[C/T]TCCTCTCCAGACTTC	89122
rs553139340	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902810	CCCTGTTTTCCACCT[A/G]CCAAACTCCTACTAA	89122
rs553291415	snp	A/C	0.00636936	0.0560724	intron-variant	TRIM4	GRCh38.p7	7:99907479	TAATTTTTTGTAAAC[A/C]TTCTGCTGGCTCACA	89122
rs553555889	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99910290	GGACAACTGGCAGGA[C/T]TTAACAAAATTTTAA	89122
rs553582605	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917767	TCATGTGTTCATGTA[A/C]TTACTGCATATCAAT	89122
rs553687428	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99894256	ATTTTGGCATCATGG[C/T]AATACAGGCCTCACA	89122
rs553887816	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899161	CTGTGTATTCAGAGT[C/T]CTGAGCTAAAGAATC	89122
rs554139347	snp	A/T	1.90293e-05	0.00308453	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892138	GGACTACAGGGAAGG[A/T]GTTTTGGTCAGGGGA	89122
rs554342049	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914576	CCAACATAAGCTGAC[C/T]GCTGCCTACATCTCG	89122
rs554380213	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99895916	TTCTTCATATTTAAT[G/T]TGTTTCTTTTCCAGT	89122
rs554394581	in-del	-/TAGT			intron-variant	TRIM4	GRCh38.p7	7:99893691	CTAACCTTCAATAGC[-/TAGT]TAGTCACCAAGTCCT	89122
rs554534036	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901930	GCGAACTCTCACTAC[G/T]TTGTTCTCCGTGAAC	89122
rs554555977	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893469	GAGGTCTCTTTTCAC[A/G]GGTTCCAGTTGTTTA	89122
rs554687132	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99892951	TTTCCCTTCTGCTCT[A/G]AAAGACTAAGCCCTA	89122
rs554691222	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99900386	TAATCTTATCCAAAA[C/T]CACCCTCAAAAAAAC	89122
rs554774641	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915126	AGGATAGCACTTTCT[C/T]TTTCTTTCCCAGCAT	89122
rs555113938	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899584	AGAACTGTATCATAG[C/T]ATACTTTCATCTCTC	89122
rs555124833	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899766	GGTGGGTGTGTGTGC[A/G]CACACGTGCATGCAT	89122
rs555292522	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906956	CAACGCAGGTAGCCA[C/T]TACCGGAAAAAGAAA	89122
rs555331472	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99914366	TCTCACAGTTGCCTA[A/G]GCTGGTCTTGAACTC	89122
rs555338246	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913882	TCTAGACCTTCAAAC[A/C]AGCTGTGCATCTGTG	89122
rs555393895	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921310	AGTATCCTTGCTAGA[G/T]GAGCTGACACTTTTT	89122
rs555431000	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920482	CCGTGATTGGCTGAA[A/G]CCCAGCTGTTATAAA	89122
rs555498531	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916929	CAAGCTCATGGCCCA[C/T]CATCCTCCTTCCCAT	89122
rs555595536	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906178	AAAATTAGAGTGTGA[A/G]AAGTCCAGAGGGAGG	89122
rs555791951	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912465	GAACCCAGAGGCAAA[A/G]GTTTCAGTGAGCCGA	89122
rs555822074	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904502	TACTAGGTAAAAACT[A/G]AGGAAATGGAAATAA	89122
rs555945473	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921476	TGTCCCTGCACCACC[A/G]TTTCAAGTATAAAAC	89122
rs555969627	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891999	ACCTCCCATGGGACT[A/G]CCTCTTGTGAAGCAC	89122
rs556053608	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99893535	AAAACTGAACTAATT[A/G]TCTTACTTACACCCC	89122
rs556090720	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900430	TTTGACCAATATCTG[C/G]GCACTCTGTGGCCCA	89122
rs556145308	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99898440	AGTAACTGTCTCCAC[A/G]TAGGGGCCCATGCCC	89122
rs556175719	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907081	AGTAGTTCTCTCAGG[C/T]TCTGAGATTCTATGT	89122
rs556175732	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915000	TTTTTAGTAAAGACA[A/G]GGTTTCACCATGTTG	89122
rs556210814	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914475	AATAACTTTTCTAAA[A/C]ACTAATCAGATATTG	89122
rs556251894	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899118	TAACTCCAGCACACC[C/G]TGAGAATAACCCTAT	89122
rs556375779	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99908986	CCTACTTGATAGCTC[C/T]GTCTAGTCATTATAG	89122
rs556464170	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899941	GACTACAGGCACACA[C/T]CAGCACACTAATTAT	89122
rs556538758	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907693	CTATCATATAAAACC[C/T]AGCTAGCAATTTCTT	89122
rs556546583	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890648	ATCACATGTTCTCAC[A/G]TATAAGGGAGAGCTA	89122
rs556563421	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891516	GAGAGAGTGCAACAT[A/G]GGCAGAGTGAGGGGG	89122
rs556660544	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905387	CAACTGATAGAAATG[C/T]ATATAAATGTGCACC	89122
rs556717232	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99913071	AGGACCAAGTTTTTG[A/G]AAGTTTTCACTTTGC	89122
rs556757989	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919785	CTGGGGGAGCCAACC[A/G]GGGAGGTGCCTATGA	89122
rs556795007	snp	G/T	0.000399281	0.0141238	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919265	TCGGGGCAGGGGAAC[G/T]GGCCGCCGCCCGGCG	89122
rs556910709	snp	A/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890613	CCTAAGCAAACCAAC[A/T]CATGAACAGAAAACC	89122
rs556924697	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892082	TCCAGGATAGAGACA[A/G/T]GAAGGGCAGAAGAGG	89122
rs557059403	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910386	AGAAATGGTCACTAT[A/G]GCATTATTCATTATC	89122
rs557115749	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99896774	TTGATGGGTGGGGCC[C/T]ACCAGGTGAGTATGG	89122
rs557171802	snp	A/G			synonymous-codon	TRIM4	GRCh38.p7	7:99892619	AGGATTCCTCCATCC[A/G]GCAAAGTAGTTCCAT	89122
rs557399698	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894816	TAATTTGTGTCTTTT[A/T]AGGACTTCATCCATT	89122
rs557411089	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902857	ACTGTCGCCTCTGCT[A/G]TGAAAACTTTCCCAT	89122
rs557464995	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM4	GRCh38.p7	7:99914715	CACAGTTCCTCAGAT[A/G]GCAGACTCTGCATCC	89122
rs557581620	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913248	TCTAAACTGGGAGGT[A/G]AGTTAACTTGACAGC	89122
rs557680473	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99913723	TTTTTAAAAATCACT[C/T]TCTCTTAATTTAGCA	89122
rs558192514	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918494	TGCTTGAACCCCGGA[G/T]GAGGAGGTTGCAGTG	89122
rs558205909	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896840	TGCTGCAGGGGGTGG[A/C]TCCAACTAAGGGAAA	89122
rs558234936	in-del	-/TTTTTCTT			intron-variant	TRIM4	GRCh38.p7	7:99914793	TCTCTGGCATAGCAC[-/TTTTTCTT]TTTTTCTTTTTTTCT	89122
rs558294449	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890711	ACAACAGACACCAGG[A/G]ACTACTTGAGGGTAG	89122
rs558331694	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897393	CGATCCCACCCTCCC[C/T]GGGATTTTACACTCT	89122
rs558408077	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99902071	ACCTCATTTGTTTCA[C/T]ATTTCTCAGGAATCA	89122
rs558703541	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909248	ATATTTAGGAAAAAG[G/T]AGGAAGGAGAGGGGT	89122
rs558830056	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99896101	TCTTTTTCTGCCTTA[-/T]TTTTTATTAATCTTT	89122
rs558978858	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99903376	CAAGACCTCCACTCC[C/T]GGTCAAAGGTTCTTA	89122
rs559039457	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99894182	TCTGAGAATTTAGGT[A/G]TCTATGTTCATGAGA	89122
rs559317865	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900878	GATTTTCTTTTTAAC[A/G]CTGGTTTCCAGCAAG	89122
rs559354607	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908196	ATGATTAAAAATAAG[C/T]GAGAAAGTTAAGTGT	89122
rs559390862	in-del	-/AAAAG	0.00517822	0.0506191	intron-variant	TRIM4	GRCh38.p7	7:99911490	TAAATTTAAAAAACT[-/AAAAG]AAAAGAAATGATTAG	89122
rs559392680	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99917478	TAATCCCAGCACTTT[A/G]GGAGGCCAAGGTGGG	89122
rs559496141	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99899906	AGCCATCCTCCCGCC[A/G]TGGCCTCCCAAGTAA	89122
rs559532549	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910627	AAATCTGGAAGGATG[C/T]ATACCCAAGTATTAA	89122
rs559560688	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915488	TCACCATAACGGGTA[C/T]AGGATGGGGATATTT	89122
rs559592782	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99914419	CCTCAGCCTCCCAAA[A/G]TGCCAGGATTATAGG	89122
rs559661882	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918874	TCGTGTTTTGCTTAA[C/T]TTCTTTGAGTTTCAG	89122
rs559982588	in-del	-/TCTC	0.00398564	0.0444627	intron-variant	TRIM4	GRCh38.p7	7:99903154	TTTCCTCTCCAGACT[-/TCTC]TCTTTATTCTCCTAT	89122
rs560091741	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99901973	TCCTCAACTCAGCAA[G/T]TCTCCCTGGCTCTAC	89122
rs560118241	snp	A/C	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892476	ATGACGTCCTCCCGA[A/C]ACACCCCAACAGCAA	89122
rs560251676	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907190	TGGCACAATCTCGGC[G/T]CACTGCAATCTCTGT	89122
rs560558676	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914075	AATATACCTCAAATC[C/T]ACCTACATGCCAAAC	89122
rs560587105	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920716	AAAAGGGGTTCTTGA[A/G]GTATCTGTTTGGGGG	89122
rs560812005	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99913534	AAATTAGCCGGGCAT[A/G]GTGGCACACGCCTGT	89122
rs560842874	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920125	CCTTAAGTGGATTTT[C/T]GATCTTGTGTTTCTG	89122
rs560861961	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891116	TAGAGCAGAAGGGTA[A/G]ACTGAGGAAAATATA	89122
rs560978307	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920844	GATCTGGTTCTTTAA[C/T]AGGGACCAAGCAGGA	89122
rs560998008	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900665	TTCTTTTAAGCTTTA[A/G]TTTACCTCCAAACTT	89122
rs561202605	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914600	CATCTCGTTTCACAT[C/T]GCATGCCACCTTTCC	89122
rs561328771	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914142	TTGTCTGACAACTAC[A/G]ATAACCTCCCGACTG	89122
rs561461433	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900190	CCCAGATAGAGCCAG[A/C]GTTCTAGTTGGAAGG	89122
rs561528559	snp	A/G	1.64958e-05	0.00287187	missense	TRIM4	GRCh38.p7	7:99892267	AAAAGGTGTGCAGGT[A/G]CACTCCGTCCACAGC	89122
rs561565438	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899302	TTAAATGGAAGGTCC[C/T]AGGTGGAGATTGCTA	89122
rs561565599	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891758	TTATACAATAAGGGC[A/G]TAATTATCTCATATA	89122
rs561584275	in-del	-/TCAGGGTTTCT	0.389152	0.207694	intron-variant	TRIM4	GRCh38.p7	7:99900929	TTTTCTTCATATTTC[-/TCAGGGTTTCT]TCATACTCAGGGTTT	89122
rs561755093	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904891	ACAAAAATTAGACAG[G/T]CATGATGGCGGGTGT	89122
rs561791794	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912635	GCATCAAAAGGAAAT[A/G]AGAATTGATGTATTC	89122
rs561837653	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918213	GATATTCCAAACTGC[C/T]ATGTGTTGTAAATGT	89122
rs561839231	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99911193	GTTGGAGCCTTGGGT[A/G]AGCGTAAAATCACCC	89122

Page 1 | 2