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

TRIM3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs10606	snp	A/G	0.303741	0.244155	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456601	CGGCACGCGCCTTCC[A/G]GTGCCAGTGGTGGAC	10612
rs1057364	snp	C/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6471558	CTGAAGGACCTGGCC[C/T]ACAGTGTGCCCAGAG	10612
rs1060067	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458091	GTGGCTGGCCGCCCT[C/T]TCTCCTGCCCCAACC	10612
rs1060069	snp	C/G/T	0.00321672	0.0399767	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456787	GGTGCTCAATCTGGG[C/G/T]GCACTGCTCACCACG	10612
rs1060070	snp	A/G	0	0	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456687	TCGCTCACTGTCACT[A/G]CCAAAGACAAGGACG	10612
rs1137113	snp	C/T			synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465638	ATGGACAAGCAGTTC[C/T]TGGTATGCAGCATCT	10612
rs1137114	snp	C/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457019	AGAAGGTGTTGCAAA[C/G]CCAGCTGGACACACT	10612
rs2303491	snp	A/C	0.209084	0.246629	intron-variant	TRIM3	GRCh38.p7	11:6457151	GTAGGTGCTGTGGGC[A/C]TCTGTGTCCTCTGTC	10612
rs2306897	snp	A/C/T	0.000133129	0.00815776	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450903	ATACCTGCAAAGTGG[A/C/T]GGTCAGTGGCCCCAC	10612
rs2344827	snp	A/G	0.295088	0.245901	intron-variant	TRIM3	GRCh38.p7	11:6464439	ctgattctccaaacT[A/G]TAACAGATTCCATAT	10612
rs2555165	snp	C/T	0.0248432	0.108648			GRCh38.p7	11:6474145	ATCCGGCTCGCCGGC[C/T]CGCCGGCTCCCTAGC	10612
rs2555166	snp	C/T					GRCh38.p7	11:6461190	CActgggcatggtgg[C/T]tcatgcctgtaatcc	10612
rs2555167	snp	A/G	0.015066	0.0854751			GRCh38.p7	11:6457891	GGAGGGGACAAAGAA[A/G]TGTGATGTCTAGCCA	10612
rs2634204	snp	C/T	0.0418186	0.138422	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449991	GACTCCCCATAGCTC[C/T]TGGGAGGAGAGCAAG	10612
rs2723617	snp	A/G	0.0441095	0.141807	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475297	ACTGGAGCATCTTGT[A/G]CTATGTGCTGAACTC	10612
rs2723627	snp	A/G	0.0256215	0.110247	intron-variant	TRIM3	GRCh38.p7	11:6464944	gtgagccgagatcgt[A/G]ccactacactccacc	10612
rs2723628	snp	A/G	0	0	intron-variant	TRIM3	GRCh38.p7	11:6465061	catacccaatgccta[A/G]aacagggtctggcac	10612
rs2723630	snp	C/T	0.0414363	0.137845	intron-variant	TRIM3	GRCh38.p7	11:6468309	gtacaatgtgtctct[C/T]tgatgtccaggtaga	10612
rs2723634	snp	C/G	0.0256215	0.110247	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473239	ACAGGAGAACCAGAG[C/G]GGTCCTTTCCTACAA	10612
rs2723636	snp	C/T	0.445893	0.155325	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448827	TGGTGACTGGGTGAG[C/T]CTGGACTGTGGTCCC	10612
rs2723637	snp	A/G	0.209084	0.246629	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448352	GCTGGGAAGGATTGT[A/G]GGGTTGGGGGGGTGA	10612
rs2723647	snp	C/T	0.456332	0.141164	intron-variant	TRIM3	GRCh38.p7	11:6458833	ACTTGTCAGGGGTCA[C/T]ACAGTATAACAGGTG	10612
rs2723650	snp	C/T	0.00398564	0.0444627	intron-variant	TRIM3	GRCh38.p7	11:6453647	TTATCAGCTCTTCTG[C/T]GAAAACTCCCTCATT	10612
rs2723663	snp	A/C	0.499598	0.0141716	intron-variant	TRIM3	GRCh38.p7	11:6462280	tgcccactagaacat[A/C]ctctgagagcaggga	10612
rs2859516	snp	C/T			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473349	cgccccTTCCATCCT[C/T]TGGTACCCACAGGCC	10612
rs3830325	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6451243	CAGCTGGACACCAGG[-/G]TAAGTAAAGTGACAG	10612
rs4758106	snp	C/G	0.498182	0.0300969	intron-variant	TRIM3	GRCh38.p7	11:6461483	cttccattacccccc[C/G]caccactctgccatc	10612
rs4758419	snp	C/G	0.298905	0.24517	intron-variant	TRIM3	GRCh38.p7	11:6466871	TGCTGTAATGTTCTT[C/G]TTACTTCTCTGCTTT	10612
rs7123791	snp	C/T	0.0908922	0.192833	intron-variant	TRIM3	GRCh38.p7	11:6472770	GAGACCTCTGCTTAA[C/T]ATAAGGAAGCTTTTC	10612
rs7129720	snp	C/T	0.0256215	0.110247	intron-variant	TRIM3	GRCh38.p7	11:6453973	GGCTCCTAGCAGTGG[C/T]GACATAGAGGGCAGG	10612
rs7932604	snp	C/T	0.0539704	0.155153	intron-variant	TRIM3	GRCh38.p7	11:6452338	CTAAGCTTTCTGGCT[C/T]TTCCTTCATAGTCAA	10612
rs7933690	snp	A/G	0.0119091	0.0762411	intron-variant	TRIM3	GRCh38.p7	11:6453478	cttcagggatctcac[A/G]gtctagtgggggaga	10612
rs7936920	snp	A/G	0.480618	0.0965156	intron-variant	TRIM3	GRCh38.p7	11:6453870	GAGAGGAGGAGGGGG[A/G]TCAGACCTCATCAGG	10612
rs7945770	snp	A/G/T	0.0670712	0.171961	intron-variant	TRIM3	GRCh38.p7	11:6452762	AAGGTACAGTTTAGC[A/G/T]GTGAGGTAATGCCCC	10612
rs7950251	snp	A/G	0.144632	0.226711	intron-variant	TRIM3	GRCh38.p7	11:6454097	CTGAAACAATGGGGA[A/G]gccaggtgcagtggc	10612
rs10128723	snp	A/C	0.00486615	0.0490856	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456833	TCCACCTCAAGGACC[A/C]GTTCCAGCTGTGCAT	10612
rs10665333	in-del	-/A/AA/AAA	0	0	intron-variant	TRIM3	GRCh38.p7	11:6454403	AAAAAAAAAAAAAAA[-/A/AA/AAA]CTATGAGGAAGTTCA	10612
rs10839566	snp	A/G	0.469544	0.119585	intron-variant	TRIM3	GRCh38.p7	11:6463257	AAATTAAAATGAAAA[A/G]TTACATTAAAAAATT	10612
rs11040895	snp	G/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6457501	GAATATCTCATTCCA[G/T]AGTTGCTGAGGGTGG	10612
rs11040896	snp	A/G	0.469642	0.119404	intron-variant	TRIM3	GRCh38.p7	11:6463049	ATCTCTACTAAAAAT[A/G]CAAAAATTAACCGGA	10612
rs11040897	snp	A/G	0.299916	0.244966	intron-variant	TRIM3	GRCh38.p7	11:6463078	GATGTGGTGGCGTGC[A/G]CCTGTAGTCCCAGCT	10612
rs11601210	snp	C/G	0.287085	0.247234	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475447	TTTCTCAACTCTATA[C/G]TTCTCCCATGCAGTC	10612
rs11601975	snp	C/T	0.285257	0.247501	intron-variant	TRIM3	GRCh38.p7	11:6471486	CAATGAAATTCATGG[C/T]CATCTCCCCCAACAT	10612
rs11603021	snp	A/G	0.284471	0.247612	intron-variant	TRIM3	GRCh38.p7	11:6463881	CTTGAATGGACAGGA[A/G]AACTGAGGCCATTTC	10612
rs11603308	snp	A/G	0.315516	0.241263	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475103	TTCCAGAGGTGGGGA[A/G]AATCCTGAAAAATTC	10612
rs11605141	snp	C/T	0.305436	0.243776	intron-variant	TRIM3	GRCh38.p7	11:6457154	AGAGGACACAGATGC[C/T]CACAGCACCTACCGA	10612
rs11605777	snp	C/T	0.473909	0.111197	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473556	AACCCCGCGCTCCCC[C/T]AAGGAACCATCACCC	10612
rs11605881	snp	A/G	0.286303	0.24735	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474370	GGAATATGCTAGTCT[A/G]TCGGCTGACCAGGAA	10612
rs11607223	snp	C/G	0.264358	0.249587	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473678	CGCCTCACGTGGGCA[C/G]AGAGAGGCACAGCTT	10612
rs11607224	snp	A/G	0.264358	0.249587	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473685	CGTGGGCAGAGAGAG[A/G]CACAGCTTTTGAAAA	10612
rs11821001	snp	C/G	0.0111196	0.0737302	intron-variant	TRIM3	GRCh38.p7	11:6452423	ACACAAGATGAACGA[C/G]AGCCAGGAGCAGCCT	10612
rs12280082	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6461090	tttgtatttttagta[A/G]agatggggttttgtc	10612
rs12294726	snp	C/G	0.309648	0.24278	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474634	AAGTGGAAAATAATT[C/G]TAACAGTTTACAGGG	10612
rs12419488	snp	A/G	0.02016	0.0983543	intron-variant	TRIM3	GRCh38.p7	11:6467864	actctggcaagctgt[A/G]agaattgaagacaaa	10612
rs12790018	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463212	tctgtctcaaaaaaa[A/C]aaaaacaaaaacaaa	10612
rs12790725	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463225	aacaaaaacaaaaac[A/C]aaaaacaaaCCaaaa	10612
rs12807424	snp	A/T	0.0314385	0.121371	intron-variant	TRIM3	GRCh38.p7	11:6461980	atttcacctcatccc[A/T]ctttactcctcactt	10612
rs13343175	snp	C/T	0.306683	0.243489	intron-variant	TRIM3	GRCh38.p7	11:6456225	TCATTCAGAGGTCAT[C/T]TTGAACCTCCCTTCC	10612
rs16913704	snp	C/T	0.0425829	0.139564	intron-variant	TRIM3	GRCh38.p7	11:6452623	CTACTAAGCTCTTCT[C/T]TGGCTGACCAGCACA	10612
rs16913732	snp	A/T	0.32627	0.238082	intron-variant	TRIM3	GRCh38.p7	11:6454709	TAGAAATAGGGTAGG[A/T]GTAAAGGACGACTGG	10612
rs16913748	snp	A/G	0.302114	0.244508	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457389	CTCGAACGCTGCACT[A/G]ATCTGGGCCAGGGCC	10612
rs17821052	snp	G/T	0.295343	0.245854	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450492	TAAAATAGAGAGGAG[G/T]CTTGTGGAAGAGGAA	10612
rs34252093	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475697	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCCCGC	10612
rs34253484	snp	A/G	0.440927	0.161391	intron-variant	TRIM3	GRCh38.p7	11:6452943	GACTAATGACCAAGT[A/G]CCACCCTCCGCCCTA	10612
rs34438642	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468082	TGAGCTCAGGAGTTC[A/G]AGATCAGTCTGGGCA	10612
rs34910224	in-del	-/C			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473494	ACCACCACCACCACC[-/C]TCGGCCGCAGCGTTC	10612
rs34965324	in-del	-/C			intron-variant	TRIM3	GRCh38.p7	11:6467185	ATGCTGTGAGAAAGA[-/C]ACACTTTTGATTGAG	10612
rs35040531	in-del	-/C			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450381	CATCACTGTATCTCC[-/C]AGCTTCTAGCATACT	10612
rs35117064	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475280	CAACCTCTTATCCAC[C/T]TGAGTTCAGCACATA	10612
rs35345984	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6468946	GCTGTGCCTTATGTT[-/G]TGTGTAAGGGTGGGC	10612
rs35484484	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475680	CTTCAGGTCTCAGCT[-/T]TTTTTTTTTTTTTTT	10612
rs35562657	in-del	-/C			intron-variant	TRIM3	GRCh38.p7	11:6450789	GGAAGTGGGATCTCC[-/C]AGAGCCAAGATATAG	10612
rs35587539	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6456009	TACATTCTATCTTTT[-/T]CAGTAGCCTGTAGCT	10612
rs35638708	in-del	-/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449789	AACACAACTCTTGAT[-/T]CCATCTCAAATCCCT	10612
rs35717222	snp	A/G	0.284471	0.247612	intron-variant	TRIM3	GRCh38.p7	11:6462533	CCACCTCAGCCTCCC[A/G]ATTAGCTAGAACTAC	10612
rs41275188	snp	A/C	0.000694839	0.0186262	intron-variant	TRIM3	GRCh38.p7	11:6457257	GCAATAACACCATCA[A/C]AATGGACGATGGTAG	10612
rs41275190	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6457531	GCTTTGCCGAACTTT[C/T]CCTTCTCCCTGGGGA	10612
rs41275192	snp	C/T	0.0409577	0.137118	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458257	GCATACTGGACAGGA[C/T]AGCGTCAGGCTCTGG	10612
rs55664515	snp	C/T	0.287346	0.247195	intron-variant	TRIM3	GRCh38.p7	11:6464941	GCAGTGAGCCGAGAT[C/T]GTGCCACTACACTCC	10612
rs55996316	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453385	TTGCTTCCTTAATAT[C/G]TCTAGAATCTGCTGG	10612
rs56024253	snp	C/G	0.114036	0.209795	intron-variant	TRIM3	GRCh38.p7	11:6468489	GCCTGGCACAAGAGA[C/G]GGGAGCCAGCAAAGG	10612
rs56046525	snp	C/G/T	0.00266112	0.0363806	intron-variant	TRIM3	GRCh38.p7	11:6457680	CCACCAGCCCAGGAC[C/G/T]CTGCCCAGTGCCTAC	10612
rs56146361	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6474034	CCCCGCCCGCCGCCG[C/T]GGAGGCCCCGCCCAC	10612
rs56202623	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453251	AGCTATCTCAAACAT[C/G]TGCAAAAGTGAATTC	10612
rs56716552	snp	C/T	0.319856	0.240042	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448323	TGGCTGTGTGCTGGG[C/T]AGAGGTCATTCCCTC	10612
rs56752241	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6461972	TCTCTCCAATTTCAC[C/T]TCATCCCACTTTACT	10612
rs58121083	snp	A/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6468742	CATGGCAGGGATTTG[A/G]TCATGAAGGGTGGCA	10612
rs58262951	in-del	-/AT	0.428182	0.17536	intron-variant	TRIM3	GRCh38.p7	11:6455268	TTCCTAATTTTACAC[-/AT]GAGTTAACTGAAGCT	10612
rs58804533	snp	A/G	0.285257	0.247501	intron-variant	TRIM3	GRCh38.p7	11:6471717	CAAATTGCTACAGCA[A/G]CAAACTGGAGGAAGT	10612
rs59935341	snp	C/T	0.0607341	0.163335	intron-variant	TRIM3	GRCh38.p7	11:6472590	TTCTCTCGGCAAGAA[C/T]GCCATTGTCTCCTAA	10612
rs60487402	snp	A/C/G	0.039204	0.134763	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475301	TCAGCACATAGCACA[A/C/G]GATGCTCCAGTGCTT	10612
rs60616451	snp	C/T	0.287346	0.247195	intron-variant	TRIM3	GRCh38.p7	11:6471923	AAAAGGCAGAGGTTA[C/T]ACATGATGCTTTTAC	10612
rs60959926	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6459906	CTGTAACAATAAACA[C/T]CCAGGTTGAGGTCAC	10612
rs61148475	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467797	GATTTTATCCTAAGT[C/T]GGAGGGGGGGATGAT	10612
rs61613299	snp	C/T	0.209084	0.246629	intron-variant	TRIM3	GRCh38.p7	11:6455231	TCATTTAACACTCCC[C/T]GCAACCCTATCAGAT	10612
rs61758091	snp	C/T	1.65999e-05	0.00288091	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457460	CTAAGGCAATTGCTG[C/T]GGACAGCTGTGGCAA	10612
rs61876782	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6455436	ACTACAAGAAACAGA[A/G]GGAAAAAAAGGCACA	10612
rs61876783	snp	A/G/T	4.94222e-05	0.00497078	missense, synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456147	ACCTTGTAAATTGGT[A/G/T]AATTCACCTTTCTCC	10612
rs61876784	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6457072	GAGCAGACTGGCACA[G/T]GGGGAGTCTCTGTGA	10612
rs61876785	snp	C/G	0.150667	0.229419	intron-variant	TRIM3	GRCh38.p7	11:6459524	TTACGTTTCTGTTAG[C/G]AGGAGAAAGGGCAAG	10612
rs61876786	snp	A/T	0.0228947	0.104514	intron-variant	TRIM3	GRCh38.p7	11:6465201	AGCAGGGAAGGACAG[A/T]CCTAACTTCAAATAT	10612
rs61876787	snp	C/G	0.145978	0.227331	intron-variant	TRIM3	GRCh38.p7	11:6466570	TCATGTCTCATAAGT[C/G]TATGATCAATCATTC	10612
rs71470010	in-del	-/A	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6454387	CAGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	10612
rs71490196	snp	C/G	0.0364509	0.129988	intron-variant	TRIM3	GRCh38.p7	11:6462979	TGGGAGGCTGAGGCG[C/G]GCAGATCACAAGGTC	10612
rs72898241	snp	A/C/T			intron-variant	TRIM3	GRCh38.p7	11:6453157	ATGGCATTTGGCACA[A/C/T]AGTAGGCATTCAACA	10612
rs72898243	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453803	TCCTCCACCATAGAA[G/T]TGTCCAAAAGAGAAA	10612
rs73400810	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6453542	AGACAAAAACAAAAA[C/T]AAACCAGTGATTCCA	10612
rs73400813	snp	A/T	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6455642	AGCCAACCTGATAAC[A/T]GCAGAGACTCCAGAC	10612
rs73400818	snp	A/C	0.00265071	0.0363088	intron-variant	TRIM3	GRCh38.p7	11:6456246	CCTCCCTTCCCTCCC[A/C]ACCCACTACCTGAGC	10612
rs73400824	snp	C/T	0.0185938	0.0946107	intron-variant	TRIM3	GRCh38.p7	11:6461691	GAATCTAGTGTTTCC[C/T]CATGCAAAACACCTT	10612
rs73400829	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6463578	CCACAGGGTCCAGGA[C/T]GGGCAGGAAAGACAG	10612
rs73400831	snp	A/C/T	0.00518109	0.0506754	intron-variant	TRIM3	GRCh38.p7	11:6465944	ATTGGGTTTCAAACC[A/C/T]GGCTCAGTCTCTCAC	10612
rs74053392	snp	C/G	0.204189	0.245767	intron-variant	TRIM3	GRCh38.p7	11:6453187	AAATGAATGAACTCC[C/G]CAGCTCAATCTCAGA	10612
rs74053396	snp	C/T	0.27861	0.248358	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465715	CCCACAGATGGCTCC[C/T]GCCACTCACACCAGC	10612
rs74053397	snp	C/T	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6465983	TGAGCTTGGACAATC[C/T]ATGTAACTTCTCTGA	10612
rs74053398	snp	A/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6469463	AGAGATTTGCCCCCA[A/G]GATCCTATAGGTGGT	10612
rs74053399	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6470669	CGCTGAAGCCTAAGA[A/G]AGAGGTCTGGCCTGG	10612
rs74053401	snp	C/T	0.0337553	0.125452	intron-variant	TRIM3	GRCh38.p7	11:6470846	AGTCTGCAAAGAAGA[C/T]TGAGAAGGCACAACC	10612
rs74055803	snp	C/T	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6471791	GAAGGGGTATTTGAG[C/T]TGGGTCTTGAGAGAC	10612
rs74055804	snp	C/G	0.0569829	0.158885	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474638	GGAAAATAATTGTAA[C/G]AGTTTACAGGGACTG	10612
rs74055805	snp	C/T	0.0821764	0.185298	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476131	GGTTACTTCTTTCCC[C/T]CAGTAGGCCCTAAGC	10612
rs74431800	snp	C/T	0.179425	0.239831	intron-variant	TRIM3	GRCh38.p7	11:6468611	GGGTGAAGTAAGAAA[C/T]GGACTGAAGAGTGCC	10612
rs74466635	snp	C/T	0.0618563	0.164627	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451897	GGTGTAATGAGGAGT[C/T]TCTTAACATTTCTAG	10612
rs74471800	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457317	TTTGGCCCCACAAAT[A/G]GTCTCCAGGTCGCTG	10612
rs74910393	snp	C/T	0.0490535	0.14873	intron-variant	TRIM3	GRCh38.p7	11:6471545	TTCAATCAAACTTCT[C/T]TGGGCACACTGTGGG	10612
rs74961578	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6463610	GAGGCCAGGACGCAG[C/T]TGGTGACTGGGAAAA	10612
rs75098223	snp	A/G	0.0314385	0.121371	intron-variant	TRIM3	GRCh38.p7	11:6453821	TCCAAAAGAGAAAAC[A/G]GTCATGTCGTGAGGA	10612
rs75321957	snp	A/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460469	ACAAAACTGAGAGGA[A/G]AAGATCTTGAGGATT	10612
rs75322667	snp	C/T	0.0260105	0.111035	intron-variant	TRIM3	GRCh38.p7	11:6461999	TACTCCTCACTTGGC[C/T]ACACTGGTTTCTTTT	10612
rs75343386	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6459176	GTGCAGGCAGAGGGG[A/G]AAGGGTAGTCCAGAT	10612
rs75363996	snp	C/T	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6461218	GTGTAACTTATTTAA[C/T]TGTGACTTACTTTTC	10612
rs75553923	snp	A/G	0.00214947	0.0327126	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457443	CTGGCTGATGCCCCC[A/G]ACTAAGGCAATTGCT	10612
rs75729314	snp	A/T	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6462211	TGTTTATATCCTGTA[A/T]AACATTAATACAAGC	10612
rs75760556	snp	A/G	0.0766824	0.180169	intron-variant	TRIM3	GRCh38.p7	11:6464030	CGGATAGAGGCAGTG[A/G]TGGTGAGAAGACCTA	10612
rs75784934	snp	A/G	0.284209	0.247648	intron-variant	TRIM3	GRCh38.p7	11:6462935	AAACAAGCTGGGCAC[A/G]GTGACTCACGCCTGG	10612
rs75833231	snp	C/T	0.0520825	0.152737	intron-variant	TRIM3	GRCh38.p7	11:6453364	ATTTAGCAAAATCTG[C/T]CATTCTTGCTTCCTT	10612
rs76070574	snp	A/C	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6470738	AAGCCATGGGCGTGG[A/C]TGACATTACCCTGAG	10612
rs76115799	snp	A/G	0.0197687	0.0974348	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473230	GCTCAGGCTACAGGA[A/G]AACCAGAGGGGTCCT	10612
rs76337493	snp	A/G	0.030665	0.119967	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448881	TGCAACCGTGGGGGT[A/G]GGGGTAGGAGAGGGA	10612
rs76906154	in-del	-/TT	0.473543	0.111932	intron-variant	TRIM3	GRCh38.p7	11:6462236	CAAGCTGCAGCTCTC[-/TT]GTTTTCTTGATTGCT	10612
rs76916255	snp	A/T	0.0611083	0.163768	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475188	AAAGTGCTGTTAGGG[A/T]TCTTTCTTGTGACCT	10612
rs77177994	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6453059	ATAACTGTTAAATAT[C/T]GGTGTCCCCTTCTAA	10612
rs77383305	snp	A/C	0.0836354	0.186609	intron-variant	TRIM3	GRCh38.p7	11:6457533	TTTGCCGAACTTTCC[A/C]TTCTCCCTGGGGAAC	10612
rs77678743	snp	A/G	0.0185938	0.0946107	intron-variant	TRIM3	GRCh38.p7	11:6454805	GGTCAGAGAGTAGCC[A/G]TCACTGAGGGAAAGG	10612
rs77730316	snp	A/C	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460797	ATAACTTAGGATCTT[A/C]ATTAAAATCTGACAA	10612
rs77737416	snp	G/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6464420	CTCCTCAGGGAAACC[G/T]TCCCTGATTCTCCAA	10612
rs77786989	snp	C/G	0.0126979	0.078662	intron-variant	TRIM3	GRCh38.p7	11:6458908	GAAGTACAGACTTCA[C/G]AGAGTGTTAGAGGAT	10612
rs77814124	snp	C/G	0.0322114	0.122752	intron-variant	TRIM3	GRCh38.p7	11:6452176	AATTAGTCCATTCAG[C/G]CTATGGGGCTGACAA	10612
rs77979367	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6466594	ATCATTCCTGCTGGG[-/T]TTTTTTTTTTTTTTT	10612
rs78015141	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6455797	CTTTGCAGTCCAGGA[A/G]CTGACCTGCCCTAAG	10612
rs78095922	snp	C/T	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6461243	CTTTTCCTTGCAGTC[C/T]TCTCAAGTAGAGTGG	10612
rs78296120	snp	C/T	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6462400	CCTTGGAAATATTTC[C/T]TTTTTTTTATTTGTT	10612
rs78406550	snp	G/T	0.0425829	0.139564	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451823	TGAGGACTTGTCCAG[G/T]GTGGCTGGACTGCAG	10612
rs78515653	snp	C/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450000	TAGCTCTTGGGAGGA[C/G]AGCAAGCCCCTTAAG	10612
rs78619512	snp	C/T	0.0252325	0.109451	intron-variant	TRIM3	GRCh38.p7	11:6463290	AATAAAAAAATAAAA[C/T]GAAGTTAATAAAGTA	10612
rs78663546	snp	A/G	0.0287284	0.116357	intron-variant	TRIM3	GRCh38.p7	11:6471900	GATGGACAAGATTGC[A/G]AATCTCCAAAAGGCA	10612
rs78667117	snp	C/T	0.0425829	0.139564	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450360	CACAGAATACATTTG[C/T]TTTGTGCATCACTGT	10612
rs78747926	snp	A/C			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473252	AGGGGTCCTTTCCTA[A/C]AAAAAAACAGCCTCC	10612
rs78811052	snp	C/T	0.108399	0.206032	intron-variant	TRIM3	GRCh38.p7	11:6456213	AAACAAAATAATTCA[C/T]TCAGAGGTCATCTTG	10612
rs79056107	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470728	ATGGTTCCTGAAGCC[A/G]TGGGCGTGGATGACA	10612
rs79199689	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468363	CAGGAGCTCAAGAGA[A/G]AAGTCTGGACTGGTT	10612
rs79355991	snp	A/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6454879	TCAGGAAGTTTAAAC[A/G]TATAGGTGTTTAGAA	10612
rs79627971	snp	C/T	0.0197687	0.0974348	intron-variant	TRIM3	GRCh38.p7	11:6467790	AAAAAGTGATTTTAT[C/T]CTAAGTTGGAGGGGG	10612
rs79663332	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475119	AATCCTGAAAAATTC[C/T]GGTTTCCTTGGCCAA	10612
rs79743696	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460220	GGACAGGAAAATGTC[C/T]ACTGAATTTGGCAAA	10612
rs79771020	snp	A/G	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6458794	TCCTGGAGCTAGGCT[A/G]CCCAGGCCCAACACC	10612
rs79794373	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454258	TAGCCAGGTATAGTG[A/G]CATGCGCCTGTAGTC	10612
rs80119108	snp	C/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6455269	TCCTAATTTTACACA[C/T]GAGTTAACTGAAGCT	10612
rs80160718	snp	A/T	0.5	0	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475105	CCAGAGGTGGGGAAA[A/T]TCCTGAAAAATTCTG	10612
rs111269723	snp	C/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6462235	TACAAGCTGCAGCTC[C/T]CGTTTTCTTGATTGC	10612
rs111290321	in-del	-/TGAA/TGAATGAA	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6468854	TTTTTCTAAAGACTG[-/TGAA/TGAATGAA]TGAATGAATGAATGA	10612
rs111380265	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6470066	TACCTGCTAGGGGAT[A/G]AAGGATTTATCCAAA	10612
rs111522761	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6455187	AATAGCTAACATCAG[A/G]AGTTTCACTAGATGT	10612
rs111604826	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475766	CTCCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	10612
rs111604890	snp	A/G	0.00597247	0.0543191	intron-variant	TRIM3	GRCh38.p7	11:6453539	ACCAGACAAAAACAA[A/G]AACAAACCAGTGATT	10612
rs111623164	snp	C/T	0.0138799	0.0821421	intron-variant	TRIM3	GRCh38.p7	11:6452308	CACCTCCTTTAATCC[C/T]CCTTCCCACTTTAGC	10612
rs111646180	snp	C/T	0.5	0	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475784	CTCCCGGGTTCACAC[C/T]ATTCTCCTGCCTCAG	10612
rs111654174	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470047	GGAGTTTAGACTTTA[C/T]GCTTACCTGCTAGGG	10612
rs111821687	snp	C/T	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6465401	TTCTTGCCCTCAAAA[C/T]CTCATTTCCTGCAGG	10612
rs111832290	snp	C/T	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6460948	TCCTGCTCTGTCACC[C/T]AGGTGTGAGTGCAGT	10612
rs111998176	snp	A/G	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6455677	TACATACATTCAGGA[A/G]CCAGGCATGCATGTT	10612
rs112139838	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6468397	GATTTGGGATCACTA[A/G]CATATAAATGGCACT	10612
rs112260825	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6463954	GAGCAGGGCTGGCAG[A/G]GAAGCAGTATCTCTG	10612
rs112489177	snp	C/T	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6469533	GCCTTGGTCTCAGAG[C/T]CAGACTTTACTCTCC	10612
rs112508925	in-del	-/T	0.5	0	frameshift-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456680	AACCGCCCGTCCTTG[-/T]CTTTGGTAGTGACAG	10612
rs112670582	snp	C/T	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6463061	AATGCAAAAATTAAC[C/T]GGATGTGGTGGCGTG	10612
rs112673053	in-del	-/TT	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6472565	CCCAACGATGGACTC[-/TT]TGCTCAAGTTCTCTC	10612
rs112833667	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6469279	GTCACACAGGGGCGG[A/G]GATTGGGCTATGTCC	10612
rs112882524	in-del	-/A	0.328148	0.237472	intron-variant	TRIM3	GRCh38.p7	11:6454387	CAGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	10612
rs113111457	snp	C/T	0.00716266	0.059414	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448394	TAGGCAAAGGACTTG[C/T]CTACTTCTGTAGGGC	10612
rs113113422	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6460991	GCTCACTGCAACCTC[C/T]ACCTCCCGGGTTCAA	10612
rs113209476	snp	A/T	0.5	0	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475193	GCTGTTAGGGATCTT[A/T]CTTGTGACCTCTCCA	10612
rs113232884	snp	C/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6462669	CTCCCACCTTGGCCT[C/G]CCAAAGTGCTGGGAT	10612
rs113523380	in-del	-/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6463554	ACTGCAGGGGAGCCA[-/G]TCGGTCAGCCACAGG	10612
rs113552781	snp	C/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6455954	ACTGCTCTTAAGGAA[C/T]GGTACTATCTGTAGG	10612
rs113596771	snp	A/T	0.5	0	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452108	GGAGGTAGGCTCATG[A/T]GACTTAGTAGCAGAC	10612
rs113625582	snp	A/G	0.00676609	0.0577691	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474862	AGCATTTGGAGACTC[A/G]GTACCTTTCATGTTG	10612
rs113740103	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473942	GGACTAGCCGCACAG[C/G]CCGGAGGGAGGGGCC	10612
rs113764375	snp	A/C	0.00636936	0.0560724	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475560	CCCTCTTCATTTTTC[A/C]TTCCAAGCAATTCCT	10612
rs113790992	snp	A/G	0.5	0	intron-variant	TRIM3	GRCh38.p7	11:6457168	CCCACAGCACCTACC[A/G]AGGGCATGTCAGGAG	10612
rs113883114	snp	C/T	0.13446	0.221699	intron-variant	TRIM3	GRCh38.p7	11:6462236	ACAAGCTGCAGCTCT[C/T]GTTTTCTTGATTGCT	10612
rs114241674	snp	C/G	1.64814e-05	0.00287061	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451334	GTCTGCCACAATTAT[C/G]TCTCCATTGGTGTCC	10612
rs114388264	snp	A/C	0.0387552	0.1337	intron-variant	TRIM3	GRCh38.p7	11:6453459	TCTGAAAGTAGATCC[A/C]TGACTTCAGGGATCT	10612
rs114701536	snp	A/G	0.0130921	0.0798413	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451657	GGATGAAGGGGAATG[A/G]TGAGAAAAGGCTCCA	10612
rs114906593	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6459317	TTAGAAGTTATCCTG[C/T]CAGCAATAGGAAGCT	10612
rs115071836	snp	C/T	0.0107246	0.0724382	intron-variant	TRIM3	GRCh38.p7	11:6470733	TCCTGAAGCCATGGG[C/T]GTGGATGACATTACC	10612
rs115111926	snp	A/G	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6469131	GAAGGACCAGGAGGC[A/G]GGAGGCAAGCTGAAG	10612
rs115283984	snp	C/T	0.00011602	0.00761554	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450918	CGGTCAGTGGCCCCA[C/T]GGCCCCCAAAACGGC	10612
rs115913709	snp	C/T	8.5081e-05	0.00652175	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457712	GGCCACGCACAGCCT[C/T]GAGCTGGCGCTGCAG	10612
rs116021814	snp	C/T	0.0244538	0.107838	intron-variant	TRIM3	GRCh38.p7	11:6460851	TAAGTGCTTCACAAG[C/T]ATTAACTTATTTAAT	10612
rs116192611	snp	A/G	0.0107246	0.0724382	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451821	CTTGAGGACTTGTCC[A/G]GTGTGGCTGGACTGC	10612
rs116277611	snp	C/T	0.0244538	0.107838	intron-variant	TRIM3	GRCh38.p7	11:6452949	TGACCAAGTACCACC[C/T]TCCGCCCTACCAAAT	10612
rs116462813	snp	C/T	1.67626e-05	0.002895	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457731	CTGGCGCTGCAGGGC[C/T]GCCTTGTGCTGCTCC	10612
rs116616770	snp	A/G	0.0146672	0.084371	intron-variant	TRIM3	GRCh38.p7	11:6462059	TTCCTCAAGGCCTTT[A/G]CACAGATTTTTCTAT	10612
rs116630862	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449134	CCATACAGTGGTTCT[A/G]CAGATGTGTTGATAT	10612
rs116989614	snp	A/C/T	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6465202	GCAGGGAAGGACAGA[A/C/T]CTAACTTCAAATATC	10612
rs117106307	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475614	ATTATATGCTAGCCT[C/T]TCTGCCTGGGATGCT	10612
rs117190058	snp	A/G	0.0178098	0.0926698	intron-variant	TRIM3	GRCh38.p7	11:6472397	CTAAATGTGTTAGAG[A/G]ATGGTCTTAGTTGCC	10612
rs117255402	snp	C/T	0.0142736	0.0832652	intron-variant	TRIM3	GRCh38.p7	11:6462910	AAAAAAAATAAAATT[C/T]AAAAAATTGAAACAA	10612
rs117376787	snp	A/G	0.0146672	0.084371	intron-variant	TRIM3	GRCh38.p7	11:6467546	CAAAGCAGGAAGATC[A/G]TTTGAGCCCAGGAAT	10612
rs117547924	snp	G/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449785	AATTAACACAACTCT[G/T]GATTCCATCTCAAAT	10612
rs117733335	snp	C/T	0.0138799	0.0821421	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451783	ACAGATTGTAAAAGG[C/T]ACAAAGTCCAGTATG	10612
rs117778770	snp	C/G	0.0260105	0.111035	intron-variant	TRIM3	GRCh38.p7	11:6458514	CCTCTCAGAAGAGCA[C/G]ACTATCCACATTCCT	10612
rs118074546	snp	A/G	0.0165278	0.0893908	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448267	AGGCTTGAACTTCAA[A/G]GATTGCTTTCATAGC	10612
rs118170613	snp	A/G	0.0189856	0.0955633	intron-variant	TRIM3	GRCh38.p7	11:6467804	TCCTAAGTTGGAGGG[A/G]GGGATGATGTGGTTT	10612
rs138000007	snp	A/G	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6454719	GTAGGAGTAAAGGAC[A/G]ACTGGACAGAACTGG	10612
rs138144597	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6468049	AGCACTTCGAGAGGC[C/T]GAGGAAGGAGGTTCA	10612
rs138160606	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448125	CACTGCAGGGAGGGG[C/T]AGCAGTCTTGGAAAT	10612
rs138183758	in-del	-/G	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6472251	TGGGAGAAGAGGGAT[-/G]TTTTCTCAAAATCTG	10612
rs138201440	snp	C/T	6.86036e-05	0.00585637	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457702	AGTGCCTACCGGCCA[C/T]GCACAGCCTCGAGCT	10612
rs138225427	snp	C/T	1.9698e-05	0.00313825	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456495	CGCGGAAGGGGCTGC[C/T]GCGCACTGGCTGTCC	10612
rs138392059	snp	A/C/G	0.000281471	0.0118603	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457791	CTCACGATGCTCCCC[A/C/G]GCGCGGCACTCACCA	10612
rs138411738	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6464451	ACTATAACAGATTCC[A/G]TATGCCAATCTCTCA	10612
rs138494974	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467251	AGCAGAATTCTGGGT[A/G]GATGGGAGAAAAATG	10612
rs138597075	snp	A/G	5.68209e-05	0.00532984	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456446	TTCACATCGTCCGGG[A/G]AAGGTGGCAGGTCCC	10612
rs138600522	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6460211	GTAAGGTAAGGACAG[C/G]AAAATGTCCACTGAA	10612
rs138673014	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6455152	TTTACAGCCTCCACC[C/T]GGACGATGATATTTT	10612
rs138688599	snp	C/T	0.000115528	0.00759938	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449021	GCCAGGCAGGGCCTC[C/T]GTACAGCTACTGGAG	10612
rs138883961	snp	C/T	0.00835141	0.0640778	intron-variant	TRIM3	GRCh38.p7	11:6462700	TACAGGCATGAGCAA[C/T]TGCACCTGGCCAGAG	10612
rs138963805	snp	C/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460333	GGAGCTTGAAAGTTC[C/G]AATGAGGAGCTGGTT	10612
rs138970540	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467686	GGGAGGATTGCTTGA[A/G]CCCAGGAGGTCGAGG	10612
rs139033769	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475979	CAGGAGTGAGCCACC[A/G]CACCTGGCCAGGTCT	10612
rs139143465	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6472031	ACCCACCCACACAAG[C/T]GAGAACCCTGGTAGT	10612
rs139185130	snp	A/G	0.0142736	0.0832652	intron-variant	TRIM3	GRCh38.p7	11:6462799	TGGTAGCCTGCACCT[A/G]TAATCCCAGCTACTC	10612
rs139291756	snp	A/G	1.65792e-05	0.00287912	intron-variant	TRIM3	GRCh38.p7	11:6457852	AACTCCATCGTCTGC[A/G]GTACAAGGACTCCAG	10612
rs139690689	in-del	-/GGA	0.0425829	0.139564	intron-variant	TRIM3	GRCh38.p7	11:6452600	ACTTTCTTCTAATGT[-/GGA]GGACCTTCTACTAAG	10612
rs139706383	snp	A/G	0.0279526	0.114869	intron-variant	TRIM3	GRCh38.p7	11:6460999	CAACCTCCACCTCCC[A/G]GGTTCAAGCGATTCT	10612
rs139735764	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465616	GGGCACTGGTACCGA[C/T]CCAGGCAGATGCTGC	10612
rs139782267	snp	A/G	0.000232825	0.0107869	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456982	GCTGCAGCTACTGCC[A/G]ATGTGTTCCTGACCC	10612
rs139873545	in-del	-/TAAGGAACGGTACTATCTG	0.306679	0.24349	intron-variant	TRIM3	GRCh38.p7	11:6455947	TTGATTCACTGCTCT[-/TAAGGAACGGTACTATCTG]TAGGGTTCCATCTTC	10612
rs139889881	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451904	TGAGGAGTTTCTTAA[C/T]ATTTCTAGGCATAGC	10612
rs139906539	snp	C/T	0.000256724	0.0113268	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456809	TTGAGCACCGATCGC[C/T]GCAGACCGTCCACCT	10612
rs140019131	snp	A/T	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6461641	CATTTCAACCATTCT[A/T]CTCTATTCTTCAGCA	10612
rs140026591	snp	C/T	0.00636936	0.0560724	intron-variant	TRIM3	GRCh38.p7	11:6458581	TACAAATGCTTCTCA[C/T]AGGAATGTGCAACTA	10612
rs140345752	snp	C/T	0.0134861	0.0810011	intron-variant	TRIM3	GRCh38.p7	11:6454076	GTTCCCTCTCAATTC[C/T]CCACTCTGAAACAAT	10612
rs140488584	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451025	GTCTACGGCCACTCC[C/T]TTGGGGCCCATGAGG	10612
rs140581811	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468917	AGATTTGGGGAGGGA[C/T]AGAAGGGCTGAGTTG	10612
rs140688200	snp	C/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6470028	GCCTTGTTGGTCTTA[C/T]TAAGGAGTTTAGACT	10612
rs140986079	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448209	TAGCCATGGAGTCTC[C/T]CACACGTAGCTACCA	10612
rs141102807	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6463904	GCCATTTCCAGTTGA[C/T]AAAGGAGAGTGGGCA	10612
rs141194112	snp	G/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6466017	TCAGTCTCTTAATTT[G/T]TAATTACAGGAATAA	10612
rs141209929	snp	C/T	0.00205078	0.031956	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456700	GGTAGTGACAGTGAG[C/T]GAGGCAGGCTGGCCC	10612
rs141315675	snp	A/T	1.65222e-05	0.00287417	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457420	TCTGCCTTGCGCTCC[A/T]GCAGCTGCTGGCTGA	10612
rs141337426	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6467276	AAAATGGTATGGGTG[A/G]GGGTGAGAAACAACA	10612
rs141388409	snp	A/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6470630	AATTCAAGTGGAGAG[A/G]TCCAGTTGGCAGTTG	10612
rs141446698	snp	A/G	0.0107246	0.0724382	intron-variant	TRIM3	GRCh38.p7	11:6467934	TACCAAAGTTCTTTG[A/G]GTAAGATAATGTAGG	10612
rs141459407	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475743	GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCCACTG	10612
rs141555418	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6464210	TAGGTGGTCTGGCCT[C/T]CACCTACCTCTCCAG	10612
rs141650905	snp	A/G	0.00438332	0.0466095	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450016	AGCAAGCCCCTTAAG[A/G]GGGCACACAAGCCTC	10612
rs141904195	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6471375	ATGACTGCAGGTTAC[A/G]GTCTTTGGGCTTTCT	10612
rs142025706	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6459907	TGTAACAATAAACAC[C/G]CAGGTTGAGGTCACC	10612
rs142278707	snp	A/T	0.000307953	0.0124049	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457726	TCGAGCTGGCGCTGC[A/T]GGGCCGCCTTGTGCT	10612
rs142505859	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6455551	TTATGGGAGAGGCAG[G/T]GGGAGGACCACCTGC	10612
rs142562495	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469827	AGCAGGGGTGGGTCC[A/G]GAGGTTGGAGGCCAA	10612
rs142644625	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6465335	AGAGAAGGCCCTATT[C/T]TTGACAGGAACCATG	10612
rs142721039	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460215	GGTAAGGACAGGAAA[A/G]TGTCCACTGAATTTG	10612
rs142846935	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6471951	TACATCCTAAAAGCA[C/T]AAAAATAAATATGCT	10612
rs142997277	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464569	TTCACTATACTGTTA[C/G]CTCTTTAAGAGTAAG	10612
rs143283093	snp	C/G	0.0126979	0.078662	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474766	AAAAATAGGGATCTT[C/G]CTCCCCAGACGTTAG	10612
rs143396438	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454939	CCCAGTAAAATGTTT[C/T]GAAGAAGTAAAGTGC	10612
rs143408397	snp	C/T	3.49046e-05	0.00417745	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456571	GTACACTAGCTCATA[C/T]GTGCCATTCTTGTGG	10612
rs143432611	snp	C/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6463926	GAGTGGGCAGTGGAG[C/G]TGGAATCTCAAAGAG	10612
rs143479802	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459076	CTGGCTCAAGCAGGT[A/G]GAGAGGGTGTCCAGG	10612
rs143565609	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6459278	AAAGTCCAAGGCAAG[A/G]AATGGTGACAGAAGT	10612
rs143625444	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461657	CTCTATTCTTCAGCA[A/G]CTTTCTTCCAAGCTC	10612
rs143703656	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471185	GGACTTCCTCCTACA[A/G]TCTCACAGGATTCCC	10612
rs143814557	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467222	GGGAAGGCTCTCCAA[C/G]GAGGTAACTTTTAAG	10612
rs143831223	snp	A/G	3.39599e-05	0.00412053	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456871	TGGCCGCTCCGGGAA[A/G]GCCTGTGCCGCCAAT	10612
rs143896388	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474999	GACTGTCTGGGAGCT[A/G]CAGTATCCATGACAA	10612
rs143918493	snp	C/T	3.29712e-05	0.00406011	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451008	ATGATATGTCCATTC[C/T]GGTCTACGGCCACTC	10612
rs143939747	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6472350	CATCTTGTACTACCT[C/T]GATGATTTGACTTCT	10612
rs144053629	snp	A/C	0.0111196	0.0737302	intron-variant	TRIM3	GRCh38.p7	11:6455595	CACTGAAAGATACCC[A/C]CTTTGGCCAAGATAC	10612
rs144175951	snp	C/T	8.33841e-05	0.0064564	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456988	GCTACTGCCGATGTG[C/T]TCCTGACCCTGGCGC	10612
rs144312526	snp	A/G/T	0.000205769	0.0101412	intron-variant	TRIM3	GRCh38.p7	11:6458053	GCCTCACTGGGCCTC[A/G/T]CTTGGGCCCACCTTG	10612
rs144485396	snp	A/G	3.31005e-05	0.00406807	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457796	GATGCTCCCCGGCGC[A/G]GCACTCACCACACAT	10612
rs144496745	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449793	CAACTCTTGATTCCA[C/T]CTCAAATCCCTCTCT	10612
rs144521953	snp	C/T	0.000577096	0.0169769	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465684	GCCAGGGCTGTCCTC[C/T]CTCTTTGCCATGGCG	10612
rs144532138	snp	C/G	0.00716266	0.059414	intron-variant	TRIM3	GRCh38.p7	11:6468925	GGAGGGATAGAAGGG[C/G]TGAGTTGCTGTGCCT	10612
rs144660078	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465067	CAATGCCTAGAACAG[A/G]GTCTGGCACATAGTA	10612
rs144748926	snp	C/T	0.0592508	0.161601	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448857	AAAGCAAGAACCGAA[C/T]AAATAAAGTGCAACC	10612
rs144792317	in-del	-/AG	0.0142736	0.0832652	intron-variant	TRIM3	GRCh38.p7	11:6460371	TGGATGGTGCTAGAA[-/AG]AGTTTTTACCTGTTT	10612
rs144869958	snp	C/T	0.0130921	0.0798413	intron-variant	TRIM3	GRCh38.p7	11:6466985	GCACAGAGCCTGACA[C/T]AAAGATTGATCTATA	10612
rs144893330	snp	C/T	0.00874735	0.0655527	intron-variant	TRIM3	GRCh38.p7	11:6453826	AAGAGAAAACGGTCA[C/T]GTCGTGAGGACCCCA	10612
rs145092543	snp	G/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6467341	AAACAGCATGATAAA[G/T]GTTCTTAGGCAGAAG	10612
rs145167262	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6470655	CAGTTGGAAAGATAC[A/G]CTGAAGCCTAAGAGA	10612
rs145197784	snp	C/T	3.36899e-05	0.00410412	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457001	TGTTCCTGACCCTGG[C/T]GCAGTGTGTCCAGCT	10612
rs145293689	in-del	-/G	0.0539704	0.155153	intron-variant	TRIM3	GRCh38.p7	11:6458814	GCCCAACACCCCGTT[-/G]GGTCACCTGTTATAC	10612
rs145361707	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475246	CACCTGGGTGCAGCA[G/T]GAGCTTTGGGAACCG	10612
rs145658560	snp	A/G	1.65168e-05	0.00287369	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451043	GGGGCCCATGAGGCG[A/G]CCAGCTCCAATCTTG	10612
rs145666188	snp	C/T	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6459147	TAAATAATTGTTAGC[C/T]TGACCAAAGAATGGT	10612
rs145866294	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6463350	GTATAAATCACTTAG[C/T]CAGTCCCTGGCAAAC	10612
rs145877594	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460074	GCAAAAACTGAATGA[C/G]GACAACAAAGAAGAC	10612
rs146086652	snp	G/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6464660	TAACAATGTATCACA[G/T]GTTCCCCATAAATAT	10612
rs146306442	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6471692	ATAAGTACCATGATA[C/T]TGACATGTTCAAATT	10612
rs146379181	snp	C/T	0.000115303	0.00759199	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465613	TTGGGGCACTGGTAC[C/T]GATCCAGGCAGATGC	10612
rs146535285	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6458554	CACACAGGCTCACCT[G/T]TCACAGGTGTTTACA	10612
rs146553443	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6453060	TAACTGTTAAATATC[A/G]GTGTCCCCTTCTAAG	10612
rs146563028	snp	C/T	0.0821764	0.185298	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475879	CATTTTTAGTAGAGA[C/T]GGGTTTTCACCGTGT	10612
rs146652084	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474791	CGTTAGCCCTCATCA[C/T]TCAGCTAGAAAGTGG	10612
rs146671401	snp	C/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6470575	CACCCAGCTAGAGTT[C/T]ACTGTTTAATGTGAT	10612
rs146779434	snp	A/G	0.000164861	0.00907764	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451016	TCCATTCCGGTCTAC[A/G]GCCACTCCCTTGGGG	10612
rs146874288	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456938	AACACCTCCGGGGCC[A/G]AGCCCAGGCGCAGTG	10612
rs146890491	snp	A/G	0.00835141	0.0640778	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475064	ATGGGAATCTGCTGA[A/G]TGGGTCTTCCCCTTC	10612
rs147004081	snp	C/T	3.85023e-05	0.00438744	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456463	AGGTGGCAGGTCCCC[C/T]GGACGCAGGGCACGC	10612
rs147132011	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6455054	ACCCCTGGCTTCTAA[C/T]AGTAATCTACCTCCA	10612
rs147152602	snp	A/G	5.20784e-05	0.00510259	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456586	TGTGCCATTCTTGTG[A/G]TCCACCACTGGCACC	10612
rs147289402	snp	A/C/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451659	ATGAAGGGGAATGGT[A/C/G]AGAAAAGGCTCCAAG	10612
rs147338905	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6455702	CATGTTGGAAGACAC[A/G]GAGGGCAGGCCACCA	10612
rs147394898	snp	G/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6469604	CCACCATACTTTATG[G/T]CTTAGTTCTCAAGGC	10612
rs147444184	snp	A/G	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6471975	ATATGCTAAAAATAA[A/G]TAAATCTAAATAAAT	10612
rs147830004	snp	A/C	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6465929	CAGACGTAGGATTAG[A/C]TTGGGTTTCAAACCT	10612
rs147980395	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449849	GTCTCGTCTTTCTCA[C/T]GGTCCAGGCTCACAT	10612
rs147986331	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6464035	AGAGGCAGTGGTGGT[A/G]AGAAGACCTAGGGAC	10612
rs148017282	snp	A/G	4.99771e-05	0.0049986	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458185	CATGAGGCTGCTGAT[A/G]AAGAAGTTGTTCTGC	10612
rs148051054	in-del	-/GGGGGGGGT			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452008	CCCAGTCAGAGGCTG[-/GGGGGGGGT]TTGCAGTATTCCAGT	10612
rs148121496	snp	C/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6471191	CCTCCTACAATCTCA[C/G]AGGATTCCCAGTACA	10612
rs148234600	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454059	GTGGAGCTATACCAG[A/G]TGTTCCCTCTCAATT	10612
rs148456994	snp	A/T	0.00478085	0.0486577	intron-variant	TRIM3	GRCh38.p7	11:6469659	ACTTGACACTGCTGC[A/T]AGGCCTGGGGACACA	10612
rs148630114	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473742	TCCGACCCAGACCCG[C/G]GCTGACAGGAATACA	10612
rs148768534	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6455901	GGCCTATGGGAATGG[A/G]GTGGCTGGTGGGTGC	10612
rs148786669	snp	C/T	4.94548e-05	0.00497242	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449041	AGCTACTGGAGGTAG[C/T]GATAGGCTTTAAAGC	10612
rs148872360	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459207	ACAGAAGGCAGCAAG[A/C]AGCAGCATAGTATGA	10612
rs148925589	snp	C/T	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6452514	ATGGACTGGTCTCCC[C/T]GCCCCGGCCCCACCC	10612
rs148981301	in-del	-/TA	0.0138799	0.0821421	intron-variant	TRIM3	GRCh38.p7	11:6461854	TACATTATTTCCCTG[-/TA]TATATATATATTTTT	10612
rs148993071	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471152	CTCCAAATTCTCAAA[C/T]AGCATTAATTTTCCC	10612
rs149045793	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6467127	GTGGCAGATATTTTA[A/G]AAGTAAATAATAGTG	10612
rs149154084	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475394	AGATGAGGGAACTGG[A/T]GTCTAGATGACACTA	10612
rs149155205	snp	A/C/T	0.000151976	0.00871587	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457003	TTCCTGACCCTGGCG[A/C/T]AGTGTGTCCAGCTGG	10612
rs149261007	snp	C/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449047	TGGAGGTAGCGATAG[C/G]CTTTAAAGCAGTGGT	10612
rs149264225	snp	A/G	0.000860457	0.0207241	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457794	ACGATGCTCCCCGGC[A/G]CGGCACTCACCACAC	10612
rs149316010	snp	A/G	3.79535e-05	0.00435607	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456450	CATCGTCCGGGGAAG[A/G]TGGCAGGTCCCCCGG	10612
rs149437579	snp	A/C	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460665	AGCAGAGGACACTTA[A/C]TAGAAACAGACATCA	10612
rs149519775	snp	A/G	0.0138799	0.0821421	intron-variant	TRIM3	GRCh38.p7	11:6472141	AGGTTTAAAAAGTTA[A/G]GAGATCTAGGATCTA	10612
rs149673466	snp	A/C	0.00597247	0.0543191	intron-variant	TRIM3	GRCh38.p7	11:6470323	AGGAATTAACAGATG[A/C]TTCTTTGGAAACTCT	10612
rs149702440	in-del	-/G	0.123798	0.215808	intron-variant	TRIM3	GRCh38.p7	11:6461298	TTAGGGCCAGAAGGT[-/G]GGCTTGAGCCCTCCC	10612
rs149798087	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452166	AGTATACAAGAATTA[A/G]TCCATTCAGGCTATG	10612
rs149908022	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6466067	AGTGCCTGTTGAGTG[C/T]ATGGTACAGAGATGT	10612
rs150077237	snp	C/T	0.000442184	0.0148626	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457767	ATCCCTCAGCAGCAC[C/T]GTGCCATGCTCACGA	10612
rs150129017	snp	A/G	3.7696e-05	0.00434127	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456439	ACGGCGCTTCACATC[A/G]TCCGGGGAAGGTGGC	10612
rs150267584	snp	C/T	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460332	GGGAGCTTGAAAGTT[C/T]CAATGAGGAGCTGGT	10612
rs150320888	snp	C/T	0.0228947	0.104514	intron-variant	TRIM3	GRCh38.p7	11:6454646	ACTATCCAGGCTGGG[C/T]CCAAATGCCTTCCTG	10612
rs150448892	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475197	TTAGGGATCTTTCTT[C/G]TGACCTCTCCACAAG	10612
rs150600851	snp	A/C	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6465409	CTCAAAACCTCATTT[A/C]CTGCAGGTTGGGGTT	10612
rs150851901	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6468032	CTCACATCTGTAATC[C/T]CAGCACTTCGAGAGG	10612
rs150968755	snp	C/T	0.00914312	0.0669923	intron-variant	TRIM3	GRCh38.p7	11:6470015	TATATCATGCAATGC[C/T]TTGTTGGTCTTATTA	10612
rs150988781	snp	A/C	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6459366	CAGGTTTATATTTTA[A/C]CAAGCTCCTCTTCAC	10612
rs151061340	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456373	CATGGAGCTGGGCCT[A/C]CGCACTGCCTTCTGG	10612
rs151216179	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462123	GAACTCAGGTCAAAT[A/G]TCACCTCCTCAGGGA	10612
rs151281368	snp	C/T	6.60731e-05	0.00574736	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457417	GCCTCTGCCTTGCGC[C/T]CCTGCAGCTGCTGGC	10612
rs180776352	snp	G/T	0.00734815	0.0601671	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451469	AAGGGGAGGGAGCAG[G/T]TAGGAGGGGAGACAC	10612
rs180790537	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6467001	AAAGATTGATCTATA[C/T]TTACTGAATTGATTT	10612
rs180897793	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6463472	GTGCAGAGACATCCA[A/G]TTTCAGCTCTGATCC	10612
rs180916961	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454363	AGCACTGTACTCCAG[A/C]CTGGACAACAGAGAC	10612
rs180928266	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6470422	GTTTTTGTTTTTTAA[A/G]AGACAGGGTCTTACT	10612
rs181426324	snp	C/G/T	0.00159649	0.0282165	intron-variant	TRIM3	GRCh38.p7	11:6466362	TGGAATACAGCAATA[C/G/T]CCTCTTAACTGGTGT	10612
rs181427131	snp	A/C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460686	ACAGACATCAGAACT[A/C/G]AAGGCAGCTGTATTT	10612
rs181544792	snp	G/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6463076	CGGATGTGGTGGCGT[G/T]CGCCTGTAGTCCCAG	10612
rs181564363	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450202	TTGTGCTTGAGGTCC[C/T]CCTCATATAGTCTTT	10612
rs181652113	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450138	GGCTCTTCCTGTGTC[C/T]TTTGTCTCAAACACT	10612
rs181661649	snp	C/G	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6465959	TGGCTCAGTCTCTCA[C/G]CAGCTATGTGAGCTT	10612
rs182013197	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471106	AGATCCTGGACATCT[A/G]CAAAGGATGTGTTTC	10612
rs182067650	snp	C/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6460132	TGTTAGGGCAGAAAA[C/G]TGAGTGGTACATTTC	10612
rs182145604	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452765	GTACAGTTTAGCGGT[A/G]AGGTAATGCCCCTCC	10612
rs182156263	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6468965	GTAAGGGTGGGCCTG[A/G]GTAGAGTGTGAAGGG	10612
rs182330978	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6457199	GCAGAATATCTAGGC[C/T]GGGGAATGGGGAGCT	10612
rs182414650	snp	A/G	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6461009	CTCCCGGGTTCAAGC[A/G]ATTCTCTTGCCTCAG	10612
rs182575269	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454791	AGGTGAAAAGCAGGG[A/G]TCAGAGAGTAGCCGT	10612
rs182752207	snp	C/G	0.00676609	0.0577691	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448321	ACTGGCTGTGTGCTG[C/G]GCAGAGGTCATTCCC	10612
rs182768378	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464617	ACCTTAAATACCCTA[C/T]TTGATTGTTACCCAT	10612
rs182895382	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468044	ATCCCAGCACTTCGA[A/G]AGGCTGAGGAAGGAG	10612
rs182908714	snp	G/T	0.00914312	0.0669923	intron-variant	TRIM3	GRCh38.p7	11:6461296	CCTTAGGGCCAGAAG[G/T]TGGGCTTGAGCCCTC	10612
rs183113349	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468509	GCCAGCAAAGGTGAC[C/T]CTGAGAAAGAGAACC	10612
rs183453539	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463984	GGTGCAGAGCCAGGT[C/T]TCCGTTGGGGCAGAA	10612
rs183454862	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451973	TGGCTGTAGGGAGAA[A/G]TCAAGACTACAAGCT	10612
rs183536970	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6472376	CTTCTAGTTTCCACT[A/G]TTAGGCTAAATGTGT	10612
rs183957813	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475987	AGCCACCGCACCTGG[C/T]CAGGTCTCAGCTTTC	10612
rs183966912	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459654	AAGAAGACCTGGATT[G/T]AGGCAATAGTAATGT	10612
rs184016105	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475282	ACCTCTTATCCACCT[G/T]AGTTCAGCACATAGC	10612
rs184159667	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6458397	TTCCCTCACAGGTGT[A/G]CCATTACACTTCATT	10612
rs184205866	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462435	TAATTTAAGATAGAG[C/T]CTCTCTCTGTCACCC	10612
rs184346980	snp	C/T	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6466069	TGCCTGTTGAGTGCA[C/T]GGTACAGAGATGTCC	10612
rs184397491	snp	A/G	0.00121581	0.0246257	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448715	GACTCCTGTCCTGGG[A/G]TAGGCTGTTCTGGCC	10612
rs184516732	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464853	TTAGCTGGGCGTGGC[A/G]GCGTGCGCCTGTAGT	10612
rs184882339	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454576	AAGGAGCTGGAAGGT[G/T]TAACTGAGTAGGGAA	10612
rs184892920	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470772	GTAAAGAGAGAAAGG[A/G]GGGTCTATCACCAAG	10612
rs184925803	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470278	AACTTGGTGGCTGGG[C/T]ATTTACATGTGAAGA	10612
rs185013122	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454207	AATATAGTGAAACCC[C/T]GTCTTTACTAAAAAT	10612
rs185030029	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449920	TCTCAGTCTTGCCTC[A/G]GCCTGAGTGATCTAA	10612
rs185046787	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465217	CCTAACTTCAAATAT[C/T]CTCCAACTAGTCATA	10612
rs185047751	snp	C/T	0.00478085	0.0486577	intron-variant	TRIM3	GRCh38.p7	11:6459065	AGGAAATGCATCTGG[C/T]TCAAGCAGGTGGAGA	10612
rs185092587	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450167	CTCTCGTCCTCCTCT[A/G]CCTTCCATTTAATTC	10612
rs185180967	snp	C/G	0.0252325	0.109451	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475749	CAGTGGCGCAATCTT[C/G]GCTCCACTGCAAGCT	10612
rs185517959	snp	C/T	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6453481	CAGGGATCTCACAGT[C/T]TAGTGGGGGAGAAAG	10612
rs185612717	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460720	GACCTCAAATTTGTG[A/G]AGTGAAGATCTGCAT	10612
rs185640983	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469353	GTTCCCCTCCCAGAC[G/T]TACTGGGCATGCAGC	10612
rs185754556	snp	A/G	0.0256215	0.110247	intron-variant	TRIM3	GRCh38.p7	11:6463113	GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC	10612
rs185763130	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6455742	GGGAGAAAGTAAGAG[A/G]CTCAAGGAGAGGCAG	10612
rs185781400	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463629	TGACTGGGAAAAGAG[A/G]GAGCAGTCAAAGGGG	10612
rs185913022	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460278	ACAGGGAGGGAGTGG[C/T]AGGAGAAGGAAAGCT	10612
rs186310483	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451711	TAGCCTAATGAGGAT[A/G]CCACATAAACCAAAT	10612
rs186333370	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450322	ACCTTTTTCTCTTCC[C/T]TACTAGACTATAATC	10612
rs186341297	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467005	ATTGATCTATATTTA[C/T]TGAATTGATTTCAGG	10612
rs186456628	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6472494	GTGACACTCTATGAA[C/T]GCTCTCTATTCTAAC	10612
rs186544522	snp	C/T	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6466476	TACTCTGTTTAAATT[C/T]CTTCAAATGTTATCC	10612
rs186583525	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468236	TGATGGGCCATGAAT[A/G]GAGACAGTGAAAGCT	10612
rs186825935	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452037	GTTGAGAAATGATGA[C/T]GGCTTGGACCAAGGA	10612
rs186942381	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474488	AAAGGTGGGGGATTT[A/G]ATTAGGCTTTGGGCG	10612
rs186948111	snp	A/C	8.46547e-05	0.00650539	intron-variant	TRIM3	GRCh38.p7	11:6457259	AATAACACCATCACA[A/C]TGGACGATGGTAGGA	10612
rs186960024	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462023	TTCTTTTCTGGTATC[C/T]GAACATGTCCTGTCT	10612
rs187176627	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6454958	GAAGTAAAGTGCATG[C/G]TAGTTAGAAACAATC	10612
rs187277973	snp	A/G	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6471447	CCAATGAATCCTTTA[A/G]ATAAGATTAGCAGGG	10612
rs187520110	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461634	ATCACTGCATTTCAA[C/G]CATTCTACTCTATTC	10612
rs187616012	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460051	AAGAGAGAGGGACAG[A/C]GCACTTAGCAAAAAC	10612
rs187684985	snp	A/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6464581	TTAGCTCTTTAAGAG[A/T]AAGCATTGTAAGTGA	10612
rs187767587	snp	A/G	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6464881	AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAGGA	10612
rs187896522	snp	A/G	0.0193772	0.0965046	intron-variant	TRIM3	GRCh38.p7	11:6468992	AGGGCATGCCTGAAA[A/G]TATCCTCTGCTGATG	10612
rs187897518	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452642	CTGACCAGCACAGCT[C/T]TTGGGTTCTGCAGTG	10612
rs187982646	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453050	TGCAGCTAAATAACT[A/G]TTAAATATCGGTGTC	10612
rs188034413	snp	A/G	0.00243309	0.034794	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448722	GTCCTGGGGTAGGCT[A/G]TTCTGGCCCCAGGCT	10612
rs188057665	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448341	AGGTCATTCCCTCAC[C/T]CCCCCAACCCCACAA	10612
rs188201710	snp	G/T	0.00716266	0.059414	intron-variant	TRIM3	GRCh38.p7	11:6468645	TAGATTTGGCTGTGG[G/T]GGGGTGGCAGGGGCA	10612
rs188342366	snp	A/C	0.00279162	0.0372561	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476374	GAGAGAAGACTGGGC[A/C]TTCAAACCATCTCTG	10612
rs188343949	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6459674	AATAGTAATGTAGAC[C/T]ATGAGGTGGAAATAA	10612
rs188355556	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464702	TGTATCAGTTTTTAA[A/G]AAGAGTAAGCACGGT	10612
rs188404021	snp	A/T	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6454261	CCAGGTATAGTGGCA[A/T]GCGCCTGTAGTCCCA	10612
rs188547530	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459219	AAGAAGCAGCATAGT[A/G]TGAATAAGCAACTGT	10612
rs188703950	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458770	TAGCATGATGATTAA[G/T]GGAATGGGTCCTGGA	10612
rs188998195	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475412	CTAGATGACACTATC[A/T]TAAGCCTCAGAGGAC	10612
rs189136749	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6461112	GGTTTTGTCATGTTG[G/T]CCAGGCTGGTCTCAA	10612
rs189175118	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6462923	TTTAAAAAATTGAAA[C/G]AAGCTGGGCACGGTG	10612
rs189290571	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466688	TCCTGGGATCCTTTT[C/T]CTGGCCCCTTTTCCT	10612
rs189329074	snp	C/T	0.000494389	0.0157146	intron-variant	TRIM3	GRCh38.p7	11:6465554	CCTCCCCAGTACACA[C/T]ATCCCCTCACCTCTC	10612
rs189366106	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6470993	CATTAACCTCAGAGC[A/C]TGTGGTTTTCAGGGG	10612
rs189370194	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454747	TGGGAATATGGCCAC[A/G]GAAGAGTCCCTTGCA	10612
rs189406285	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450064	TCCCCTCCTCAAGCT[A/G]AGTCTGAACTACTTG	10612
rs189609373	snp	A/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450180	CTGCCTTCCATTTAA[A/T]TCCCACTTGTGCTTG	10612
rs189719182	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470369	TGGATGAGAGGGTGA[C/T]AAGTTTGGTGTTTAT	10612
rs189817013	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6451204	CCAGACCCTGACCAC[C/T]AAGAGGCACTAGACT	10612
rs189874529	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466192	GCAGCTCTTCCATTT[A/G]TACCCTGACCCACCT	10612
rs190048743	snp	A/C/T	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6472623	GGCTGTGGCAGTACC[A/C/T]GGCACACAGGAAGTA	10612
rs190136933	snp	C/G	0.000342836	0.0130882	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456780	TGGCGCTCGTGGTGA[C/G]CAGTGCGCCCAGATT	10612
rs190184939	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6469705	AGCTCAGCCTTCATG[A/G]ATTCCACAATCTAAT	10612
rs190254456	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6460096	AAAGAAGACCAGGCC[A/G]AGAGGCAGGAAGAGC	10612
rs190598327	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460385	AAGAGTTTTTACCTG[C/T]TTGGCATGGGAGTTT	10612
rs190626266	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448152	AAATGTGAGAAAGGG[G/T]ATATGTCAGGGCTCC	10612
rs190642490	snp	A/T	0.0107246	0.0724382	intron-variant	TRIM3	GRCh38.p7	11:6464594	AGTAAGCATTGTAAG[A/T]GATGGATACCTTAAA	10612
rs190650732	snp	C/T	0.0193772	0.0965046	intron-variant	TRIM3	GRCh38.p7	11:6462660	CAAGTGATCCTCCCA[C/T]CTTGGCCTCCCAAAG	10612
rs190773101	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451856	AGCACCCAGGTGAAC[A/C]AAAGAAGGAATTATG	10612
rs190783700	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6467086	GATAAAACAGACAGG[G/T]TCACTGTCCCTGTGG	10612
rs191002116	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6463835	AACCAACAGGCACAA[A/G]AGGGTGGTTGTCCCC	10612
rs191061882	snp	A/C	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6463211	CTCTGTCTCAAAAAA[A/C]CAAAAACAAAAACAA	10612
rs191161133	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6460990	GGCTCACTGCAACCT[A/C]CACCTCCCGGGTTCA	10612
rs191405500	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474948	CCCAAAAATCAAGCT[C/T]TAGTCAGATGATTGC	10612
rs191422512	snp	C/T	0.000132072	0.00812518	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449349	ACAATGATGTTTCCA[C/T]TGGAGTCCACAGCTA	10612
rs191487212	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6468818	GTCACCATTGTCTGT[A/G]CTGTTGGATGCATTA	10612
rs191515540	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475817	TCCCGAGTAGCTGGG[A/G]CTACAGGACTACAGG	10612
rs191524521	snp	A/G	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6459427	AATGAGACAGCAGAT[A/G]GGGTTGGGGGGCGAG	10612
rs191549566	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452392	CATACACTCTGCTTT[A/G]TTATAGGCTCTGGGG	10612
rs191567735	snp	C/T	0.00478085	0.0486577	intron-variant	TRIM3	GRCh38.p7	11:6452715	ATACCATGAGCTCCA[C/T]GAGCTAAATAGTAGA	10612
rs191721767	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471891	TATGGAACAGATGGA[A/C]AAGATTGCAAATCTC	10612
rs191787959	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461280	TCTCATACTCCACAC[C/T]CCTTAGGGCCAGAAG	10612
rs191824278	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468329	GTCCAGGTAGAGCTG[C/T]CAAGTAAGAAACAGA	10612
rs192002688	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455184	AACAATAGCTAACAT[C/T]AGAAGTTTCACTAGA	10612
rs192093653	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461759	ACCTGGCTCACGATA[A/G]CTTCCTAACTGGTCT	10612
rs192376535	snp	A/C	0.00517822	0.0506191	intron-variant	TRIM3	GRCh38.p7	11:6469276	ACTGTCACACAGGGG[A/C]GGGGATTGGGCTATG	10612
rs192381016	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453381	ATTCTTGCTTCCTTA[A/G]TATCTCTAGAATCTG	10612
rs192537705	snp	C/T	0.00557542	0.0525036	intron-variant	TRIM3	GRCh38.p7	11:6464852	GTTAGCTGGGCGTGG[C/T]GGCGTGCGCCTGTAG	10612
rs192639396	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6464939	TTGCAGTGAGCCGAG[A/G]TCGTGCCACTACACT	10612
rs192749030	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6462062	CTCAAGGCCTTTGCA[A/C]AGATTTTTCTATTGC	10612
rs192825592	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448594	TGCAGCCCCACCCCA[A/C]AAGAACCCAGCAAAA	10612
rs192858052	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6453817	AGTGTCCAAAAGAGA[A/G]AACGGTCATGTCGTG	10612
rs192939933	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475741	CTGGAGTGCAGTGGC[A/G/T]CAATCTTGGCTCCAC	10612
rs193069514	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469942	TTTTGCATCAGGAGG[C/T]TGAATCAGACACTGT	10612
rs193168499	snp	G/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6458883	AAGGACTCTTCCTTT[G/T]TAAGATGGAGAAGTA	10612
rs199550708	in-del	-/A	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473252	GGGGTCCTTTCCTAC[-/A]AAAAAAACAGCCTCC	10612
rs199586229	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456309	TACCAACACGGAAGA[C/G]GAGCTCATCCTCAAT	10612
rs199634071	in-del	-/C	0.0146672	0.084371	intron-variant	TRIM3	GRCh38.p7	11:6454420	TATGAGGAAGTTCAG[-/C]CCCCTCACCAGGACA	10612
rs199667872	in-del	-/AATG			intron-variant	TRIM3	GRCh38.p7	11:6468888	ATGAATGAATGAATG[-/AATG]CAGGAGCGAGTCTAG	10612
rs199812847	snp	C/T	3.30551e-05	0.00406528	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465712	GCGCCCACAGATGGC[C/T]CCCGCCACTCACACC	10612
rs199921289	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6450624	ACAAAATGGGGCCCT[A/G]AAAATACAAAGTGGT	10612
rs200119903	snp	A/G	6.65812e-05	0.00576942	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449399	CTGCCCATTGCCCTC[A/G]CCATGGGAGCCAAAC	10612
rs200144942	snp	C/T	0.000372402	0.0136405	intron-variant	TRIM3	GRCh38.p7	11:6457264	CACCATCACAATGGA[C/T]GATGGTAGGAAAGGG	10612
rs200203203	snp	C/T	0.000100624	0.00709238	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465713	CGCCCACAGATGGCT[C/T]CCGCCACTCACACCA	10612
rs200239046	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457696	CTGCCCAGTGCCTAC[C/T]GGCCACGCACAGCCT	10612
rs200316045	snp	C/T	0.000249362	0.0111633	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458206	GTTGTTCTGCAGTGC[C/T]GAGACGCCCTGCTCT	10612
rs200372830	snp	A/C	0.006978	0.0586542	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465725	GCTCCCGCCACTCAC[A/C]CCAGCCTCTGTATGG	10612
rs200430322	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6466591	TCAATCATTCCTGCT[-/G]GGTTTTTTTTTTTTT	10612
rs200480674	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474471	AAGGAGTTAAGGGGT[A/G]GAAAGGTGGGGGATT	10612
rs200528455	snp	A/G	3.30022e-05	0.00406202	intron-variant	TRIM3	GRCh38.p7	11:6456057	GTGGTGGAGGAGAGC[A/G]GTAAAGGTGCTTACC	10612
rs200552983	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6469345	CTGCTTCAGTTCCCC[-/T]CCCAGACTTACTGGG	10612
rs200613645	in-del	-/CT			intron-variant	TRIM3	GRCh38.p7	11:6462231	TAATACAAGCTGCAG[-/CT]CTCTCGTTTTCTTGA	10612
rs200710201	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475881	TTTTTAGTAGAGATG[A/G]GTTTTCACCGTGTTA	10612
rs200727893	snp	A/C	1.69378e-05	0.00291009	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456880	CGGGAAGGCCTGTGC[A/C]GCCAATGCAGCCAGC	10612
rs200787297	snp	A/G	9.9425e-05	0.00705001	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457781	CTGTGCCATGCTCAC[A/G]ATGCTCCCCGGCGCG	10612
rs200914624	snp	A/G	0.00443152	0.0468628	intron-variant	TRIM3	GRCh38.p7	11:6457524	GAGGGTGGCTTTGCC[A/G]AACTTTCCCTTCTCC	10612
rs201064815	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6466593	AATCATTCCTGCTGG[G/T]TTTTTTTTTTTTTTT	10612
rs201134419	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6456042	AAAACTCTTATTTTG[A/G]TGGTGGAGGAGAGCG	10612
rs201189234	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6472613	TCTCCTAAGTGGCTG[G/T]GGCAGTACCTGGCAC	10612
rs201406536	snp	A/G	0.000652724	0.0180537	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458087	TCATGGTTGGGGCAG[A/G]AGAGAGGGCGGCCAG	10612
rs201483503	in-del	-/CC			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475804	TCCTGCCTCAGCCTC[-/CC]GAGTAGCTGGGACTA	10612
rs201517377	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6456240	CTTGAACCTCCCTTC[A/C]CTCCCCACCCACTAC	10612
rs201616021	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6466592	AATCATTCCTGCTGG[-/T]GTTTTTTTTTTTTTT	10612
rs201671612	snp	C/G	0.000102638	0.00716299	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456813	GCACCGATCGCCGCA[C/G]ACCGTCCACCTCAAG	10612
rs201759803	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6472689	AATCTCTGCAGTTCC[C/G]TTTCATCAGAGAGAG	10612
rs201984032	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6457075	CAGACTGGCACAGGG[G/T]GAGTCTCTGTGATTA	10612
rs202036047	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6462892	AAGACACTCATCTCT[-/A]AAAAAAAAAATAAAA	10612
rs202101398	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6464028	TGCGGATAGAGGCAG[G/T]GGTGGTGAGAAGACC	10612
rs202246105	snp	C/T	1.71779e-05	0.00293064	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457700	CCAGTGCCTACCGGC[C/T]ACGCACAGCCTCGAG	10612
rs267603105	snp	C/G			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456493	CACGCGGAAGGGGCT[C/G]CCGCGCACTGGCTGT	10612
rs367637221	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450024	CCTTAAGGGGGCACA[C/T]AAGCCTCACTCTCAG	10612
rs367705048	snp	G/T	5.29984e-05	0.00514746	intron-variant	TRIM3	GRCh38.p7	11:6456260	CCACCCACTACCTGA[G/T]CCTGGCCCATCTGGC	10612
rs367777871	snp	C/T	6.61813e-05	0.00575207	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457440	CTGCTGGCTGATGCC[C/T]CCGACTAAGGCAATT	10612
rs367890878	snp	C/T	1.64817e-05	0.00287064	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450547	AGGGAGGGAAGACAC[C/T]GACCTTCACTGAATG	10612
rs367956214	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474512	TTGGGCGCTTCAGGA[A/G]CCCCCTCCTGAGGAA	10612
rs368017492	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471689	GTGATAAGTACCATG[A/G]TATTGACATGTTCAA	10612
rs368057290	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6459439	GATGGGGTTGGGGGG[C/T]GAGGGCAGTGGCATC	10612
rs368164162	snp	C/G	9.25215e-05	0.0068009	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456410	TGGCTGCCGGGGCCG[C/G]CAGGGGACTTGACAC	10612
rs368225353	in-del	-/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449907	ATTGATCTTCCTGTC[-/T]CAGTCTTGCCTCAGC	10612
rs368232244	snp	A/G	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6454617	CCTCATTACTCCCCC[A/G]CAATCCCCTCCTCAC	10612
rs368338923	snp	A/C	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6468109	GGCAACATAATGAGA[A/C]CCCATCTCTATAAAA	10612
rs368340141	snp	C/T	4.96266e-05	0.00498105	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457815	CTCACCACACATGGC[C/T]GTCTCACAGGCCTCA	10612
rs368500294	snp	A/G	3.29571e-05	0.00405924	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449060	AGGCTTTAAAGCAGT[A/G]GTTGCCAGCATCAGC	10612
rs368527287	snp	A/C	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6454901	TGTTTAGAAGTAAGG[A/C]TCTTCAGCGAAAAGT	10612
rs368530909	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476357	GCTCCAACTGAGGCT[A/G]GGAGAGAAGACTGGG	10612
rs368628123	snp	C/T	3.29565e-05	0.00405921	intron-variant	TRIM3	GRCh38.p7	11:6449193	TACCTGGGGAAGGAG[C/T]GCAGAAAGGAGGGAG	10612
rs368637616	snp	C/T	0.00835141	0.0640778	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451943	GATCAATTTTGCTTT[C/T]AAGAAAGAACATTCT	10612
rs368647461	in-del	-/CT	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476148	AGTAGGCCCTAAGCA[-/CT]GTGGGCAGGGACCGT	10612
rs368687872	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450151	TCTTTTGTCTCAAAC[A/G]CTCTCGTCCTCCTCT	10612
rs368755396	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6460306	GCTTGACTGCTGGAA[-/G]TTGAGTGAAGGGGAG	10612
rs369119820	snp	A/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450951	ACCAGTTTGCCATTG[A/G]GCTGGAAGGTAAAGA	10612
rs369174014	in-del	A/GCCACCCT			intron-variant	TRIM3	GRCh38.p7	11:6452943	GACTAATGACCAAGT[A/GCCACCCT]CCACCCTCCGCCCTA	10612
rs369204101	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452155	AGAGAGGAGAAAGTA[C/T]ACAAGAATTAGTCCA	10612
rs369209345	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6468663	GTGGCAGGGGCAGAA[-/A]GCCACGTCAGAGTGA	10612
rs369222896	snp	A/G/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6466912	TGCAGTGTTATTGAG[A/G/T]ATAGGCATTTTATTT	10612
rs369226155	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452978	ATCAATATGCACATA[C/T]AAACTTAGGTCACCA	10612
rs369340382	snp	A/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6455161	TCCACCTGGACGATG[A/T]TATTTTTAACAATAG	10612
rs369363384	snp	C/T	1.69289e-05	0.00290933	intron-variant	TRIM3	GRCh38.p7	11:6457260	ATAACACCATCACAA[C/T]GGACGATGGTAGGAA	10612
rs369443709	in-del	-/C			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475258	CAGGAGCTTTGGGAA[-/C]CCGCCTCAACCTCTT	10612
rs369541577	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475361	TGCAGTTTTGGGCTG[C/G]GGCTACTATGCTACC	10612
rs369544681	snp	A/T	1.71985e-05	0.0029324	intron-variant	TRIM3	GRCh38.p7	11:6458310	ATCTGTCCAGGAAGG[A/T]GAGTCAAAGAACAGA	10612
rs369634962	snp	C/T	1.84422e-05	0.00303657	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456402	GGCGCACATGGCTGC[C/T]GGGGCCGCCAGGGGA	10612
rs369726925	snp	A/G	8.83619e-05	0.00664629	intron-variant	TRIM3	GRCh38.p7	11:6457057	AGGGGAGGAGTGGGT[A/G]AGCAGACTGGCACAG	10612
rs369751213	snp	A/G			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TRIM3	GRCh38.p7	11:6448641	ATTTATTTAATATGG[A/G]GGGTGGGGTATTGCT	10612
rs369765128	snp	A/G	1.66023e-05	0.00288113	intron-variant	TRIM3	GRCh38.p7	11:6451220	AAGAGGCACTAGACT[A/G]GTCAGTTCAGCTGGA	10612
rs369781461	snp	A/G	1.64909e-05	0.00287144	intron-variant	TRIM3	GRCh38.p7	11:6456063	GAGGAGAGCGGTAAA[A/G]GTGCTTACCTGAATA	10612
rs369916626	snp	A/G	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6470659	TGGAAAGATACGCTG[A/G]AGCCTAAGAGAGAGG	10612
rs369921459	snp	C/T	3.29614e-05	0.00405951	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451341	ACAATTATGTCTCCA[C/T]TGGTGTCCACTGCCA	10612
rs370197917	in-del	-/TGAATGAA			intron-variant	TRIM3	GRCh38.p7	11:6468855	TTTTTCTAAAGACTG[-/TGAATGAA]TGAATGAATGAATGA	10612
rs370205863	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6460285	GGGAGTGGCAGGAGA[-/A]GGAAAGCTTGACTGC	10612
rs370231567	snp	A/G	3.53269e-05	0.00420265	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458086	TTCATGGTTGGGGCA[A/G]GAGAGAGGGCGGCCA	10612
rs370231602	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466732	CCTACTCATCTTTCA[A/G]GTCCCCATATAAATG	10612
rs370343478	snp	C/T	1.66568e-05	0.00288585	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457473	TGCGGACAGCTGTGG[C/T]AATCTGGAGGGGGAA	10612
rs370378188	snp	C/T	0.000155209	0.00880796	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456610	TGGCACCGGAAGGCG[C/T]GTGCCGTCCGGGCCG	10612
rs370455474	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6462790	ACCTGGGTGTGGTAG[C/G]CTGCACCTGTAATCC	10612
rs370579436	snp	A/G	5.02938e-05	0.00501442	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465699	CCTCTTTGCCATGGC[A/G]CCCACAGATGGCTCC	10612
rs370596015	in-del	-/G/GGG	0.00255273	0.0356349	frameshift-variant, cds-indel, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449317	CACCTGGATGCGGCT[-/G/GGG]GTTGCCCCAGTCAGC	10612
rs370607471	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6468794	AAAATAGGCAATGAA[C/T]AGGACCAGGTCACCA	10612
rs370831106	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6453195	GAACTCCCCAGCTCA[A/G]TCTCAGACCTGAACT	10612
rs370929567	in-del	-/GAAAG			intron-variant	TRIM3	GRCh38.p7	11:6459861	GAGGAGTAGCTATAG[-/GAAAG]TTCAGCCTTGTCCTG	10612
rs370951694	snp	A/G	3.2956e-05	0.00405918	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449175	GGAGCCAGAGCTGTC[A/G]AATACCTGGGGAAGG	10612
rs370984008	snp	A/G	0.00755907	0.0610114	intron-variant	TRIM3	GRCh38.p7	11:6463085	TGGCGTGCGCCTGTA[A/G]TCCCAGCTACTTGGG	10612
rs371008569	snp	C/T	1.75182e-05	0.00295953	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449451	GCACTGTACACCTGG[C/T]GGGGGAAGGGGCTAG	10612
rs371055478	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6469887	ACTCCTAAAGAAAGT[A/G]ACGTTCAAGCTGAGG	10612
rs371126337	snp	A/C	1.65214e-05	0.0028741	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457311	CTTCTGTTTGGCCCC[A/C]CAAATGGTCTCCAGG	10612
rs371131254	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456126	GCCGCTGCTGGCTGC[A/G]GACACACCTTGTAAA	10612
rs371161551	snp	C/T	0.000461893	0.0151899	intron-variant	TRIM3	GRCh38.p7	11:6465517	GGAGGAGGATCCTCA[C/T]CCTCCCCACAGGGTC	10612
rs371457884	snp	A/G	1.70755e-05	0.00292189	intron-variant	TRIM3	GRCh38.p7	11:6458303	TGGAGACATCTGTCC[A/G]GGAAGGAGAGTCAAA	10612
rs371527147	multinucleotide-polymorphism	GGG/TGT			intron-variant	TRIM3	GRCh38.p7	11:6470537	GCCTGCCAAAGCGTG[GGG/TGT]GTTGCAGGCATGAGC	10612
rs371544938	snp	G/T	5.33946e-05	0.00516667	intron-variant	TRIM3	GRCh38.p7	11:6456272	TGAGCCTGGCCCATC[G/T]GGCTCTGCCCTCGGC	10612
rs371550914	snp	A/C	8.26112e-05	0.00642641	intron-variant	TRIM3	GRCh38.p7	11:6449265	GCATATGGGACACAC[A/C]AGGAAACCGCCCCCT	10612
rs371742245	snp	A/G	3.372e-05	0.00410595	intron-variant	TRIM3	GRCh38.p7	11:6457500	GGAATATCTCATTCC[A/G]GAGTTGCTGAGGGTG	10612
rs371884729	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470524	TCCTCCTGCCTTGGC[C/T]TGCCAAAGCGTGGGG	10612
rs372054040	snp	C/G	0.000115814	0.0076088	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457825	ATGGCCGTCTCACAG[C/G]CCTCACAGTAAAACT	10612
rs372091658	snp	A/G	1.65622e-05	0.00287764	intron-variant	TRIM3	GRCh38.p7	11:6450650	GTGGTCTTCAGGGCA[A/G]TAAGCTGGGATGCTG	10612
rs372204401	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6459882	TCAGCCTTGTCCTGG[C/T]TGAATTTACTGTAAC	10612
rs372217012	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6472660	ATATGTTGGTTACAG[A/G]AGAGCTCTGTTTAAA	10612
rs372283699	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6449254	TGGGGGAACGGGCAT[A/G]TGGGACACACCAGGA	10612
rs372369027	snp	C/T	3.32779e-05	0.00407895	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456981	AGCTGCAGCTACTGC[C/T]GATGTGTTCCTGACC	10612
rs372591012	snp	A/G	1.65559e-05	0.00287709	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457447	CTGATGCCCCCGACT[A/G]AGGCAATTGCTGCGG	10612
rs372611156	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6472579	CTTTGCTCAAGTTCT[C/T]TCGGCAAGAATGCCA	10612
rs372680385	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449682	TGGGAAATCAGTTCT[C/G]TTAGTTCTCTATCTC	10612
rs372693830	snp	A/G	5.09264e-05	0.00504585	intron-variant	TRIM3	GRCh38.p7	11:6457245	GGAACAATGGAGGCA[A/G]TAACACCATCACAAT	10612
rs372856589	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476434	GCTCTTTTGACTTGA[C/T]AGGGTTCTGGTGTTT	10612
rs372879493	snp	C/T	0.000149508	0.00864474	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458260	TACTGGACAGGATAG[C/T]GTCAGGCTCTGGGCA	10612
rs372891120	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6466663	GGAGATCAGGCATTC[A/G]TTCTCTCTGTCCTGG	10612
rs372969093	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464835	GTAATAAAATACAAA[A/G]AGTTAGCTGGGCGTG	10612
rs372977800	snp	A/C/G	0.00043777	0.0147891	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458098	GCAGGAGAGAGGGCG[A/C/G]CCAGCCACTACACTG	10612
rs373202919	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6467779	TCTCAAAAAAAAAAA[-/A]GTGATTTTATCCTAA	10612
rs373213679	snp	A/T	8.79237e-05	0.00662979	intron-variant	TRIM3	GRCh38.p7	11:6457654	CGAGCTAAGACACCA[A/T]CCCTGTGGCCCCACC	10612
rs373259054	snp	C/G	0.000153988	0.00877328	intron-variant	TRIM3	GRCh38.p7	11:6451241	TTCAGCTGGACACCA[C/G]GGTAAGTAAAGTGAC	10612
rs373279475	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6461445	TTCCAATTGTGGACA[C/T]CTTTCTCTTGGCTCA	10612
rs373456046	in-del	-/CTTT			intron-variant	TRIM3	GRCh38.p7	11:6460898	TTGTTTTTTTGGTGG[-/CTTT]TTTTTTTTTTTTTTT	10612
rs373498059	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6467698	TGAGCCCAGGAGGTC[A/G]AGGCTGCAGTGAGCC	10612
rs373524727	snp	A/G	1.81086e-05	0.00300898	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456545	AGCAGCTCGCCTTCC[A/G]TGCGCGCTGTGTACA	10612
rs373644501	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449001	CAATGTCTGTCCCTC[C/T]ACAAGCCAGGCAGGG	10612
rs373731291	in-del	-/AGGAACGGTACTATCTGTA			intron-variant	TRIM3	GRCh38.p7	11:6455949	GATTCACTGCTCTTA[-/AGGAACGGTACTATCTGTA]GGGTTCCATCTTCCA	10612
rs373823449	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6463449	CAGTGATCTGGGCAC[A/T]GGAGAAAGTGCAGAG	10612
rs373824947	snp	C/T	1.72359e-05	0.00293558	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456659	TCAGCGCTGCCTGTG[C/T]GCACCAACCGCCCGT	10612
rs373855786	snp	C/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6461565	ACCTTCTCACCCCCA[C/G]TGATCTTTTCCCCCA	10612
rs373938787	in-del	-/CTT	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6465770	CCAGGGAGTCCAGAA[-/CTT]CTTCTCCCCACCCAA	10612
rs374021380	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464563	TTCTCTTTCACTATA[C/T]TGTTAGCTCTTTAAG	10612
rs374170222	snp	C/G	0.000330126	0.0128434	intron-variant	TRIM3	GRCh38.p7	11:6465522	AGGATCCTCATCCTC[C/G]CCACAGGGTCCTCAT	10612
rs374241194	snp	C/T	3.60711e-05	0.00424668	intron-variant	TRIM3	GRCh38.p7	11:6458339	GAGTGGGTGGGGTGG[C/T]ATAAGTGCACCCTTC	10612
rs374643027	snp	C/T	1.80071e-05	0.00300054	intron-variant	TRIM3	GRCh38.p7	11:6457080	TGGCACAGGGGGAGT[C/T]TCTGTGATTACTGAA	10612
rs374709046	snp	A/G	0.000125968	0.00793526	intron-variant	TRIM3	GRCh38.p7	11:6456285	TCTGGCTCTGCCCTC[A/G]GCTGTCTGTACCAAC	10612
rs374991437	snp	C/T	0.000116699	0.00763779	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458180	GCCTCCATGAGGCTG[C/T]TGATGAAGAAGTTGT	10612
rs375086522	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6460892	TTGTTTTTGTTTTTT[A/T]GGTGGCTTTTTTTTT	10612
rs375190700	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470410	TTTTTCAGTTTTGTT[C/T]TTGTTTTTTAAGAGA	10612
rs375381622	snp	C/T	5.01375e-05	0.00500662	intron-variant	TRIM3	GRCh38.p7	11:6457889	AATGGCTAGACATCA[C/T]ACTTCTTTGTCCCCT	10612
rs375414839	snp	C/T	0.000153988	0.00877328	intron-variant	TRIM3	GRCh38.p7	11:6450852	GGGAGTTCTCTGGAA[C/T]AGGGGTATCAGCATA	10612
rs375500679	snp	C/G	0.00019771	0.00994062	intron-variant	TRIM3	GRCh38.p7	11:6449189	CGAATACCTGGGGAA[C/G]GAGTGCAGAAAGGAG	10612
rs375600890	snp	A/G	0.000168118	0.00916683	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457000	GTGTTCCTGACCCTG[A/G]CGCAGTGTGTCCAGC	10612
rs375726390	snp	A/G	3.29794e-05	0.00406061	intron-variant	TRIM3	GRCh38.p7	11:6456064	AGGAGAGCGGTAAAG[A/G]TGCTTACCTGAATAC	10612
rs375910885	snp	A/C/T	0.000154762	0.00879547	intron-variant	TRIM3	GRCh38.p7	11:6457523	TGAGGGTGGCTTTGC[A/C/T]GAACTTTCCCTTCTC	10612
rs376023603	snp	A/C	0.000153988	0.00877327	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456548	AGCTCGCCTTCCGTG[A/C]GCGCTGTGTACACTA	10612
rs376098931	snp	C/G	3.29897e-05	0.00406125	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457347	GACCAGAGCCTGCTT[C/G]CGCTGCTGCAGTGCT	10612
rs376138614	snp	A/G	0.00795532	0.062565	intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6473102	CCTGGGGTGCAGCCT[A/G]CCCCTCCAACCTGCA	10612
rs376209359	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474511	TTTGGGCGCTTCAGG[A/G]GCCCCCTCCTGAGGA	10612
rs376260971	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6455949	GATTCACTGCTCTTA[A/G]GGAACGGTACTATCT	10612
rs376417069	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6468475	GTGATAAGAAAAGGG[C/T]CTGGCACAAGAGAGG	10612
rs376476239	snp	C/T			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456991	ACTGCCGATGTGTTC[C/T]TGACCCTGGCGCAGT	10612
rs376501688	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470922	AGAAGAGAACTTCAT[A/G]AACAAGGGAGTGAAA	10612
rs376602675	in-del	-/CCCTCCCCACAGGGGAGGAGGATCCTCA			intron-variant	TRIM3	GRCh38.p7	11:6465489	ACACATGCTCCCTCA[-/CCCTCCCCACAGGGGAGGAGGATCCTCA]TCCTCCCCACAGGGT	10612
rs376638019	snp	A/G	6.60295e-05	0.00574547	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449342	GTCAGCCACAATGAT[A/G]TTTCCATTGGAGTCC	10612
rs376689505	snp	A/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451288	TGAACTTGCCCTCAG[A/G]GGAGAAGATGCTGAC	10612
rs376703451	snp	G/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6460223	CAGGAAAATGTCCAC[G/T]GAATTTGGCAAATGT	10612
rs376959049	snp	A/G	0.00996239	0.0698709	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448680	CAGTGTGTATAGGGT[A/G]GTAGGGAGACAACTA	10612
rs377025537	snp	A/G	4.98178e-05	0.00499063	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458254	CCGGCATACTGGACA[A/G]GATAGCGTCAGGCTC	10612
rs377385285	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6469679	CTGGGGACACAAAGA[C/G]AAATAGTCACAGCTC	10612
rs377571948	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6468241	GGCCATGAATAGAGA[A/C]AGTGAAAGCTGAGGT	10612
rs377606044	snp	A/G	1.7081e-05	0.00292237	intron-variant	TRIM3	GRCh38.p7	11:6458304	GGAGACATCTGTCCA[A/G]GAAGGAGAGTCAAAG	10612
rs377655559	snp	A/G	1.68846e-05	0.00290552	intron-variant	TRIM3	GRCh38.p7	11:6457266	CCATCACAATGGACG[A/G]TGGTAGGAAAGGGTG	10612
rs377709390	snp	A/G	1.80182e-05	0.00300146	intron-variant	TRIM3	GRCh38.p7	11:6458340	AGTGGGTGGGGTGGC[A/G]TAAGTGCACCCTTCC	10612
rs386373014	in-del	-/AA			intron-variant	TRIM3	GRCh38.p7	11:6454402	AAAAAAAAAAAAAAA[-/AA]ACTATGAGGAAGTTC	10612
rs386750277	multinucleotide-polymorphism	CT/GC			intron-variant	TRIM3	GRCh38.p7	11:6461483	CTTCCATTACCCCCC[CT/GC]ACCACTCTGCCATCA	10612
rs397724929	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475697	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCCCGC	10612
rs397835884	in-del	-/TT			intron-variant	TRIM3	GRCh38.p7	11:6466608	TTTTTTTTTTTTTTT[-/TT]TCCAGTTCCTGGAAA	10612
rs397849221	in-del	-/TT			intron-variant	TRIM3	GRCh38.p7	11:6466609	TTTTTTTTTTTTTTT[-/TT]CCAGTTCCTGGAAAA	10612
rs527248016	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6470664	AGATACGCTGAAGCC[C/T]AAGAGAGAGGTCTGG	10612
rs527313471	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471473	CAGGGAAGGAAAGCA[A/G]TGAAATTCATGGCCA	10612
rs527314652	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464530	TAATCTGGCTATATG[A/G]TTATTTGATGACTAT	10612
rs527372859	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458424	CATTTTAAAACCTCT[C/T]TGCTTGACACATCTC	10612
rs527373586	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6464882	GTCCCAGCTACTCCG[A/G]AGGCTGAGGCAGGAG	10612
rs527434404	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458818	CAACACCCCGTTGGT[C/T]ACCTGTTATACTGTA	10612
rs527510158	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6453108	GCATAAGGACTGCAT[C/T]TGTTTTGTTTGCTGC	10612
rs527576579	in-del	-/AAGTA	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6454944	TAAAATGTTTCGAAG[-/AAGTA]AAGTGCATGGTAGTT	10612
rs527634110	in-del	-/CCTCACCCTCCCCACAGGGGAGGAGGAT	0.00597247	0.0543191	intron-variant	TRIM3	GRCh38.p7	11:6465484	GGTTTACACATGCTC[-/CCTCACCCTCCCCACAGGGGAGGAGGAT]CCTCATCCTCCCCAC	10612
rs527782809	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468612	GGTGAAGTAAGAAAC[A/G]GACTGAAGAGTGCCC	10612
rs527787671	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472315	TCCACAGATTGTACC[A/G]TGAGCCCATGATTAA	10612
rs527845427	snp	C/T	1.65373e-05	0.00287548	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465700	CTCTTTGCCATGGCG[C/T]CCACAGATGGCTCCC	10612
rs527911024	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6466057	AGTGTGACATAGTGC[C/T]TGTTGAGTGCATGGT	10612
rs527922211	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466268	GTATCAAGGTCGGGA[C/T]TGCTTCCTGAATATC	10612
rs528033541	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463268	AAAAGTTACATTAAA[A/C]AATTAAAATAAAAAA	10612
rs528196542	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475711	TTGAGATGGAGTCCC[G/T]CTCTGTTGCCCAGGC	10612
rs528235329	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468577	AAAGAAATCAACAGA[A/G]CAGTGCAAGAAAAAG	10612
rs528242042	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476275	GGTCAGCAAACCCAA[C/T]CCCCTCTGGATCTGG	10612
rs528295682	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6469024	AGACACTGGCATCCT[A/G]ATGTTCTCTCTACAG	10612
rs528501149	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6451180	AGGAGGAGGTAGGAT[C/T]GGATCAGTCCAGACC	10612
rs528554494	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451766	GCATTCAAGCAGAGT[G/T]AACAGATTGTAAAAG	10612
rs528918313	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476426	TGGCCCCAGCTCTTT[G/T]GACTTGATAGGGTTC	10612
rs529037984	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469941	CTTTTGCATCAGGAG[A/G]CTGAATCAGACACTG	10612
rs529074054	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463746	ATAAGATTCTGGATT[A/T]TAAGATTCAGGGCAT	10612
rs529133913	snp	C/T	1.7105e-05	0.00292441	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457704	TGCCTACCGGCCACG[C/T]ACAGCCTCGAGCTGG	10612
rs529205816	snp	C/T	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458143	CTCCGGGTCGTGGGC[C/T]CCATCAGGTGCCTGC	10612
rs529226832	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6458625	CAACTTCTTTAACTC[A/T]TTAACACTACTGTCT	10612
rs529267740	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452370	ACATTACTCACTACA[A/T]AAGTCTCATACACTC	10612
rs529521832	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470726	AGATGGTTCCTGAAG[A/C]CATGGGCGTGGATGA	10612
rs529600929	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6468068	GAAGGAGGTTCACTT[G/T]AGCTCAGGAGTTCGA	10612
rs529612802	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6454378	CCTGGACAACAGAGA[C/T]CCTGTCTCAAAAAAA	10612
rs529780217	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448682	GTGTGTATAGGGTGG[C/T]AGGGAGACAACTAGA	10612
rs529858374	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471242	ATGGAGGTAACCAAG[A/G]CATTGTTGAAAATGG	10612
rs530212344	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455634	AACTGTCTAGCCAAC[C/T]TGATAACTGCAGAGA	10612
rs530270482	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6469343	TCCTGCTTCAGTTCC[C/T]CTCCCAGACTTACTG	10612
rs530336279	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450156	TGTCTCAAACACTCT[C/T]GTCCTCCTCTGCCTT	10612
rs530429606	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6449248	CTGTTTTGGGGGAAC[A/G]GGCATATGGGACACA	10612
rs530592686	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475225	AAGGTTCAGATTTAG[G/T]CTCAACACCTGGGTG	10612
rs530654511	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475561	CCTCTTCATTTTTCA[A/T]TCCAAGCAATTCCTC	10612
rs530895491	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462279	CTGCCCACTAGAACA[C/T]CCTCTGAGAGCAGGG	10612
rs530952287	snp	G/T	0.00117953	0.0242564	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456400	CTGGCGCACATGGCT[G/T]CCGGGGCCGCCAGGG	10612
rs531074874	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450945	CGGCCAACCAGTTTG[C/T]CATTGGGCTGGAAGG	10612
rs531136673	snp	A/T	0.00279162	0.0372561	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451684	TCCAAGAGAAGAAGA[A/T]GTCTGAACAAATAGC	10612
rs531164964	in-del	-/T/TT/TTTT	0.00398564	0.0444627	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475679	CCTTCAGGTCTCAGC[-/T/TT/TTTT]TTTTTTTTTTTTTTT	10612
rs531354163	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458847	TATGACCCCTGACAA[A/G]TTACATAACTTTGAC	10612
rs531357872	snp	C/T	0.000132035	0.00812404	intron-variant	TRIM3	GRCh38.p7	11:6465523	GGATCCTCATCCTCC[C/T]CACAGGGTCCTCATC	10612
rs531416855	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459400	CTCTGTGTGGGGAGT[C/G]AATTTAAAGGGAATG	10612
rs531459723	in-del	-/C	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6454611	CACCACCTCATTACT[-/C]CCCCCGCAATCCCCT	10612
rs531540837	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6454259	AGCCAGGTATAGTGG[C/T]ATGCGCCTGTAGTCC	10612
rs531554456	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458139	GGTCCTCCGGGTCGT[A/G]GGCCCCATCAGGTGC	10612
rs531703151	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467431	GAGTTTGGGAAGATA[A/G]GTAGAGATGAGATCA	10612
rs531836794	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6474150	GGAGCCGGCGGGCCG[A/G]CGAGCCGGATCCCGG	10612
rs531895339	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461547	TGATTTCTTAATTCC[C/T]TGACCTTCTCACCCC	10612
rs531926651	snp	A/G	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6455465	CATTTCCTGGCTTTG[A/G]AAAGGAGCTCACAGT	10612
rs531953948	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6461021	AGCGATTCTCTTGCC[C/T]CAGCCTCCCGAGCAG	10612
rs531963704	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459570	ACAGCAGTAGGTGCT[A/G]AAGCCTGTCTTCAAA	10612
rs532157026	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460173	TGAGTAGTCATCAGC[A/G]TTAAAAGCAGCTGAC	10612
rs532221340	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454288	CCCAGCTACTCGGGA[G/T]GCTGAAGTAGGAGGA	10612
rs532348959	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448566	AGCTAGTCCCACCAT[C/T]CCATCTCCTCACTGC	10612
rs532487167	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6461080	CTGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	10612
rs532513527	snp	C/G	0.00438332	0.0466095	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474306	GGAGCCTGTCTGGGC[C/G]GCCTGCCTCCTGGAG	10612
rs532654098	snp	A/C	3.30338e-05	0.00406397	intron-variant	TRIM3	GRCh38.p7	11:6449292	CCCTCATGTCATTCC[A/C]AGGCCTTACTCACCT	10612
rs532690352	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461640	GCATTTCAACCATTC[C/T]ACTCTATTCTTCAGC	10612
rs532755069	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455519	GTGCGGTTGATGCCA[C/T]AATCAGGTGTATGAG	10612
rs532991049	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470012	AGATATATCATGCAA[C/T]GCCTTGTTGGTCTTA	10612
rs533043169	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452506	CTTCCTTAATGGACT[C/G]GTCTCCCCGCCCCGG	10612
rs533045311	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463878	GAACTTGAATGGACA[A/G]GAAAACTGAGGCCAT	10612
rs533058603	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470654	GCAGTTGGAAAGATA[C/T]GCTGAAGCCTAAGAG	10612
rs533190354	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452952	CCAAGTACCACCCTC[C/T]GCCCTACCAAATCAA	10612
rs533281321	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6455761	AAGGAGAGGCAGAAG[C/G]AAAGGAGGAATGAGC	10612
rs533738325	snp	A/C	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6463910	TCCAGTTGATAAAGG[A/C]GAGTGGGCAGTGGAG	10612
rs533741821	snp	C/T			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451412	GACCCCAAAACGGAA[C/T]TTGAACTGGCCCTCA	10612
rs533750138	snp	A/G/T	4.97157e-05	0.00498556	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457450	ATGCCCCCGACTAAG[A/G/T]CAATTGCTGCGGACA	10612
rs533836683	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451884	ATGTTTTATCCTGGG[C/T]GTAATGAGGAGTTTC	10612
rs533894793	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6472380	TAGTTTCCACTGTTA[A/G]GCTAAATGTGTTAGA	10612
rs533912653	snp	G/T	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6471130	GTGTTTCAAGGCTTT[G/T]CAGTTTCTCCAAATT	10612
rs533942283	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452533	CCGGCCCCACCCCAA[C/T]TCCATCTCTTAGTCC	10612
rs533965126	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464715	AAAAAGAGTAAGCAC[A/G]GTAGCTCACGCCTGT	10612
rs534094887	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459109	AGTCTTCAGAGAGTT[C/G]ATGCAAACTAAATCT	10612
rs534158729	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453437	ATCTCTCTCCTATAC[C/G]ATGGTATCTGAAAGT	10612
rs534238431	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471860	TAAAGAAACAGAAAC[A/G]TGAGAAACTAAGAAA	10612
rs534359029	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6467316	GAAGGGAAATCATTC[C/T]AGGCTGAAGAAACAG	10612
rs534417173	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468034	CACATCTGTAATCCC[A/G]GCACTTCGAGAGGCT	10612
rs534428381	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6470460	CCAGGCTGGAATGTG[A/G]TGTTATGATCATAGC	10612
rs534535915	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462498	CTGCAGCCTCCACCT[C/T]CCAGGCTCAAATGAT	10612
rs534603455	snp	A/G	0.000395961	0.014065	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456652	ACGCAGCTCAGCGCT[A/G]CCTGTGCGCACCAAC	10612
rs534670133	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450346	TATAATCAAGAAGAC[A/G]CAGAATACATTTGCT	10612
rs534913875	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449839	TGCATACACTGTCTC[A/G]TCTTTCTCACGGTCC	10612
rs535080237	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475757	CAATCTTGGCTCCAC[C/T]GCAAGCTCCGCCTCC	10612
rs535113956	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462030	CTGGTATCTGAACAT[A/G]TCCTGTCTACTTCTT	10612
rs535174150	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462599	TCTTTTTTAGAGACT[C/G]CATCTCACTATGTTG	10612
rs535276380	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469540	TCTCAGAGCCAGACT[C/T]TACTCTCCTTTCTCA	10612
rs535609973	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449743	TCACTCTTGACTCCA[A/G]TTTCTTCTCTGTTTG	10612
rs535647902	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470235	AGACAGGCCAAGATA[A/T]ATCAATTTTGCAGGG	10612
rs535656209	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450434	ATAAATGTGTAAATG[C/T]GTATTGTTTGAGTGA	10612
rs535700718	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454467	TTTTTCTGTGCATGT[A/G]AGCAGTGAGCACACC	10612
rs536143101	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6472618	TAAGTGGCTGTGGCA[C/G]TACCTGGCACACAGG	10612
rs536210960	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454716	AGGGTAGGAGTAAAG[A/G]ACGACTGGACAGAAC	10612
rs536401963	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449559	ACCCAGATCTACAGC[C/T]ACAGCCCAAATCTGC	10612
rs536417329	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473445	CCCTTCAGACAAGAT[A/G]GGCCACAATATTCCA	10612
rs536484613	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466282	ATTGCTTCCTGAATA[C/T]CTTAAACCCTTCTCT	10612
rs536545266	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460529	AGGACTGGACGTCAG[C/T]CTCTGAATGGAGGGA	10612
rs536731342	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448876	TAAAGTGCAACCGTG[A/G]GGGTGGGGGTAGGAG	10612
rs536758217	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466423	ATCTTCCTTGAAGCC[A/C]GAATGAATTTTCTAA	10612
rs536759628	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474554	GACCATCCAGCGACT[A/C]CCTTCCTCACACCAA	10612
rs536813800	in-del	-/AT			intron-variant	TRIM3	GRCh38.p7	11:6471208	GGATTCCCAGTACAC[-/AT]GAGTTACACAGTTGT	10612
rs537289173	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461268	GAGTGGTTTCTGTCT[C/T]ATACTCCACACTCCT	10612
rs537342328	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455181	TTTAACAATAGCTAA[C/T]ATCAGAAGTTTCACT	10612
rs537393745	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448959	GTCTGGCCCACCTCC[C/T]AGCCAGACCCTCTTG	10612
rs537402751	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455669	AGACAGACTACATAC[A/C]TTCAGGAGCCAGGCA	10612
rs537456154	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449759	TTTCTTCTCTGTTTG[A/G]TAGGCCAATGAATTA	10612
rs537468194	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450259	TCCCACAGTTCCCTG[C/G]ACCTTCCTATCACAG	10612
rs537744058	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468680	CCACGTCAGAGTGAC[A/T]GAAGAGTAAATGGGA	10612
rs537799435	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458475	GCCTTGCCCCTTACA[A/G]CTGAGTAGGAACACA	10612
rs537947148	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6459745	TGTCTGATTAGATAT[A/G]GGGAGCAAGAGAGAT	10612
rs537951196	in-del	-/TAC	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6455420	TAGGCTCTGAGCTTT[-/TAC]TACAAGAAACAGAGG	10612
rs538076467	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6458887	ACTCTTCCTTTGTAA[G/T]ATGGAGAAGTACAGA	10612
rs538125090	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6453612	CTGAGAAGAATGTGA[C/T]TTAACATTCTGCCTA	10612
rs538127762	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448174	CAGGGCTCCAGGGAT[C/T]CAGGGATGACTTTTA	10612
rs538328055	in-del	-/TGAA			intron-variant	TRIM3	GRCh38.p7	11:6468858	TCTAAAGACTGTGAA[-/TGAA]TGAATGAATGAATGA	10612
rs538612143	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6467074	TAGGAATGGAATGAT[-/A]AAACAGACAGGGTCA	10612
rs538747432	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464048	GTGAGAAGACCTAGG[A/G]ACCAGGCCACCCAAG	10612
rs538870437	snp	A/G	0.000202532	0.0100611	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448854	ACCAAAGCAAGAACC[A/G]AATAAATAAAGTGCA	10612
rs538873992	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472446	TGCCCCCTCGCCCCC[A/G]TAAATAAATGTTTGC	10612
rs538935326	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465861	AAGACAGGGCAGTGA[C/T]TGGAAGGATCAGGGT	10612
rs538935400	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473233	CAGGCTACAGGAGAA[C/G]CAGAGGGGTCCTTTC	10612
rs539210070	snp	A/G	1.68627e-05	0.00290363	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451472	GGGAGGGAGCAGGTA[A/G]GAGGGGAGACACTGT	10612
rs539412764	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469320	AGCTCCTCCCCCACT[A/C]CTCCCCTTCCTGCTT	10612
rs539487162	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470346	GAAACTCTCAAAGAA[A/G]AGCAGTTTGGATGAG	10612
rs539671459	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6458580	TTACAAATGCTTCTC[A/C]TAGGAATGTGCAACT	10612
rs539817669	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6450805	AGAGCCAAGATATAG[A/G]AGGAGAGGGCCTTTA	10612
rs540051695	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465101	GCTCAATAAATGAAT[A/G]TTTGTTAAATGAATA	10612
rs540099992	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469861	TTCTCCTAAAGAAAG[C/T]AACTTTAGTAACTCC	10612
rs540125977	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6452740	AGTAGAAGTGAGGGG[A/G]CACTAAAAGGTACAG	10612
rs540205552	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464253	ATACTCTCAGTCACA[C/T]TCACTCTGCTCTAGC	10612
rs540252196	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451507	ACAGACAGAAGGGAG[G/T]AGGATCCTGAGGGAG	10612
rs540324662	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458655	TACTCTTGCCAAATT[C/T]ATGCCAAGCCCTGGG	10612
rs540528710	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470466	TGGAATGTGGTGTTA[C/T]GATCATAGCTCACTG	10612
rs540603568	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466561	TCTACAACCTCATGT[C/G]TCATAAGTCTATGAT	10612
rs540772515	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6461361	ACTCTAGCTCCTTTG[A/T]AGCTCATGCCTTCTA	10612
rs540900580	in-del	-/A	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6455439	ACAAGAAACAGAGGG[-/A]AAAAAAGGCACATTT	10612
rs541064301	snp	G/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6460880	ATTGTGTTTTCTTTG[G/T]TTTTGTTTTTTTGGT	10612
rs541113706	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475413	TAGATGACACTATCT[C/T]AAGCCTCAGAGGACT	10612
rs541125396	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454848	CTGGATCGATGACAT[A/G]AGTACTCAAGCAGGG	10612
rs541396158	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6461479	TCTTCTTCCATTACC[C/G]CCCGCACCACTCTGC	10612
rs541457809	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6455369	CCTGAGCTTTTAACT[G/T]CTCTGCTGTGTCAAC	10612
rs541519152	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455917	GTGGCTGGTGGGTGC[A/G]TAAGGGGTGATCCTT	10612
rs541613978	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449919	GTCTCAGTCTTGCCT[C/T]AGCCTGAGTGATCTA	10612
rs541616612	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468805	TGAATAGGACCAGGT[C/T]ACCATTGTCTGTGCT	10612
rs541618521	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462142	CCTCCTCAGGGAAGC[A/C]TTCCTTGATGACTAT	10612
rs541654171	snp	A/T	0.000249052	0.0111563	intron-variant	TRIM3	GRCh38.p7	11:6456224	TTCATTCAGAGGTCA[A/T]CTTGAACCTCCCTTC	10612
rs541686692	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462772	CCTCTCTAATATGGG[A/G]ATACCTGGGTGTGGT	10612
rs541750655	snp	A/C/G	1.67607e-05	0.00289483	intron-variant	TRIM3	GRCh38.p7	11:6457488	CAATCTGGAGGGGGA[A/C/G]TATCTCATTCCAGAG	10612
rs541804095	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475962	CCAAAGTGCTGGGAT[C/T]ACAGGAGTGAGCCAC	10612
rs541900491	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6449233	CAGGCAGATGAGAGT[C/T]TGTTTTGGGGGAACG	10612
rs542129818	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475507	CTTCTCCAGAGGGCA[A/G]AAGTCCTTAACCAGC	10612
rs542365700	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459966	AAGAGATGGGCATGC[C/T]ATCAACATTTAGATG	10612
rs542383879	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6463436	CTCCAGGAGTGCTCA[A/G]TGATCTGGGCACAGG	10612
rs542421414	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6466662	GGGAGATCAGGCATT[C/T]GTTCTCTCTGTCCTG	10612
rs542445243	snp	A/G	3.3145e-05	0.0040708	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450919	GGTCAGTGGCCCCAC[A/G]GCCCCCAAAACGGCC	10612
rs542490766	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453684	AAGCTTAGACAATTA[C/T]ACAAGGACATAATAT	10612
rs542612482	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6460589	GCACTAGGGACATAG[A/G]AGAGTGAAGGATGGA	10612
rs542652331	snp	A/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6471990	ATAAATCTAAATAAA[A/T]AAATAAATAAAAGGC	10612
rs542745367	snp	A/G	6.65192e-05	0.00576673	intron-variant	TRIM3	GRCh38.p7	11:6457870	ACAAGGACTCCAGTC[A/G]GGTAATGGCTAGACA	10612
rs542751353	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465490	CACATGCTCCCTCAC[C/T]CTCCCCACAGGGGAG	10612
rs542874309	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6460050	TAAGAGAGAGGGACA[G/T]AGCACTTAGCAAAAA	10612
rs542909687	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6469926	CAGAGAGTATGGTGC[A/C]TTTTGCATCAGGAGG	10612
rs542928947	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474861	CAGCATTTGGAGACT[C/T]GGTACCTTTCATGTT	10612
rs543028948	snp	C/T	3.29707e-05	0.00406008	intron-variant	TRIM3	GRCh38.p7	11:6465548	CTCATCCCTCCCCAG[C/T]ACACACATCCCCTCA	10612
rs543193014	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6474120	CTGCGGACGCTGCCT[C/T]CTTGGTGCTGCTAGG	10612
rs543445342	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465956	ACCTGGCTCAGTCTC[G/T]CACCAGCTATGTGAG	10612
rs543708668	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455507	CATGTTCATTCAGTG[A/C]GGTTGATGCCATAAT	10612
rs543759736	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462115	TATCCTCAGAACTCA[A/G]GTCAAATGTCACCTC	10612
rs543888034	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474231	TGTAGTCGGTCTCAG[A/G]GATTGAGATGAGACT	10612
rs543940066	snp	A/G	3.35059e-05	0.0040929	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457732	TGGCGCTGCAGGGCC[A/G]CCTTGTGCTGCTCCA	10612
rs543971634	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467578	GGAGATCAGCCTGGG[A/C]AACATAATGAGACCA	10612
rs544016290	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471989	AATAAATCTAAATAA[A/G]TAAATAAATAAAAGG	10612
rs544126030	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6464416	ATTGCTCCTCAGGGA[A/G]ACCTTCCCTGATTCT	10612
rs544174819	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6458732	TACAGAGAAAAAAGT[C/T]ACAGGAATAGTACAG	10612
rs544188719	in-del	-/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6467760	GAGACAAAGTTGAGA[-/T]TCTGTCTCAAAAAAA	10612
rs544194455	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6459254	AGTTTGATGTGGCTG[A/G]CTAGAGACAAAGTCC	10612
rs544235422	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452945	CTAATGACCAAGTAC[A/C]ACCCTCCGCCCTACC	10612
rs544280823	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470773	TAAAGAGAGAAAGGA[A/G]GGTCTATCACCAAGT	10612
rs544342304	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6467019	ACTGAATTGATTTCA[G/T]GAATTCAATAAATAT	10612
rs544505181	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6464804	ACAGCCTGAGCAACA[C/T]GGTGAAACCCCATCT	10612
rs544518543	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472012	ATAAAAGGCACCACC[A/C]CTCACCCACCCACAC	10612
rs544917447	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458799	GAGCTAGGCTGCCCA[C/G]GCCCAACACCCCGTT	10612
rs544959608	in-del	-/AA			intron-variant	TRIM3	GRCh38.p7	11:6465010	AAAAAAAAAAAAAAA[-/AA]GAGTAAGGATCTTAT	10612
rs545100486	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454053	AAGAGAGTGGAGCTA[C/T]ACCAGGTGTTCCCTC	10612
rs545142792	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471388	ACAGTCTTTGGGCTT[C/T]CTCTGAAACAAATGA	10612
rs545204320	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471936	TATACATGATGCTTT[C/T]ACATCCTAAAAGCAT	10612
rs545204389	snp	A/G	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6464856	GCTGGGCGTGGCGGC[A/G]TGCGCCTGTAGTCCC	10612
rs545250816	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472704	CTTTCATCAGAGAGA[A/G]ATGCAAAAGTAATGG	10612
rs545265667	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465422	TTCCTGCAGGTTGGG[A/G]TTCACCTGCTCTCCT	10612
rs545292952	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6459312	GGAGCTTAGAAGTTA[C/T]CCTGCCAGCAATAGG	10612
rs545311526	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466011	TGAGCCTCAGTCTCT[G/T]AATTTGTAATTACAG	10612
rs545311712	snp	A/C	0.00159617	0.0282053	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TRIM3	GRCh38.p7	11:6473935	CGCCGCCGGACTAGC[A/C]GCACAGGCCGGAGGG	10612
rs545357561	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455964	AGGAACGGTACTATC[C/T]GTAGGGTTCCATCTT	10612
rs545433268	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471696	GTACCATGATATTGA[C/T]ATGTTCAAATTGCTA	10612
rs545494291	snp	A/C/G	0.000263719	0.0114801	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450530	TGGGACAGTGGTCAC[A/C/G]GAGGGAGGGAAGACA	10612
rs545700638	in-del	-/T/TT	0.300926	0.244758	intron-variant	TRIM3	GRCh38.p7	11:6466593	ATCATTCCTGCTGGG[-/T/TT]TTTTTTTTTTTTTTT	10612
rs545710947	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468991	AAGGGCATGCCTGAA[A/C]GTATCCTCTGCTGAT	10612
rs545768238	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469734	ATAAATAGATTACTG[C/T]AATGTAAAGTGGTGA	10612
rs545915303	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6463556	TGCAGGGGAGCCAGT[C/T]GGTCAGCCACAGGGT	10612
rs545982703	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457627	CCCAGACCCTTTATT[A/C]CCCTCCCCGCCCGAG	10612
rs545988655	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6450695	GAGTATCTGGGAAGA[C/T]AAAAGCTAGGGTGTT	10612
rs546155317	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6462972	AGAACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	10612
rs546156881	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463561	GGGAGCCAGTCGGTC[A/C]GCCACAGGGTCCAGG	10612
rs546197830	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475792	TTCACACCATTCTCC[C/T]GCCTCAGCCTCCCGA	10612
rs546292125	snp	A/G			synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465627	CCGATCCAGGCAGAT[A/G]CTGCATACCAGGAAC	10612
rs546310365	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468592	ACAGTGCAAGAAAAA[G/T]AAGGGGTGAAGTAAG	10612
rs546342967	snp	C/T	0	0	intron-variant	TRIM3	GRCh38.p7	11:6457977	ATCCAGAGCAGTACC[C/T]TGTCACCCAGCCACT	10612
rs546371933	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469044	TCTCTCTACAGTTGT[A/C]ATGGGTTCTGGAGTC	10612
rs546373692	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462530	CTCCCACCTCAGCCT[A/C]CCGATTAGCTAGAAC	10612
rs546384583	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451704	GAACAAATAGCCTAA[C/T]GAGGATGCCACATAA	10612
rs546433325	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463063	TGCAAAAATTAACCG[A/G]ATGTGGTGGCGTGCG	10612
rs546546997	in-del	-/CTGG	0.00557542	0.0525036	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448307	TTCTCTCTGCACCTA[-/CTGG]CTGTGTGCTGGGCAG	10612
rs546698623	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476287	CAACCCCCTCTGGAT[A/C]TGGTGCTCTTAAGAT	10612
rs546718494	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6458574	AGGTGTTTACAAATG[C/T]TTCTCATAGGAATGT	10612
rs546939081	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6470181	TTTAAAGGGCAAGGA[C/T]GGAAAATTAAGAAAC	10612
rs546953043	snp	A/G	1.65373e-05	0.00287548	intron-variant	TRIM3	GRCh38.p7	11:6456047	TCTTATTTTGGTGGT[A/G]GAGGAGAGCGGTAAA	10612
rs547119159	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454298	CGGGAGGCTGAAGTA[A/G]GAGGATTGCTTGAGC	10612
rs547644815	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6455593	GCCACTGAAAGATAC[A/C]CCCTTTGGCCAAGAT	10612
rs547655203	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6466392	TTCTTGTCTCCTCAC[C/T]GACACCTTTTCATTT	10612
rs547706472	snp	A/G	3.30327e-05	0.0040639	intron-variant	TRIM3	GRCh38.p7	11:6449293	CCTCATGTCATTCCC[A/G]GGCCTTACTCACCTG	10612
rs547878124	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455017	CTCCATCTCCAAAAC[C/T]AATTACAATCTGACC	10612
rs547893884	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6472788	AAGGAAGCTTTTCCA[C/T]AGCAGAAAGTAGCAA	10612
rs548133754	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448164	GGGGATATGTCAGGG[C/T]TCCAGGGATTCAGGG	10612
rs548356261	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474509	GCTTTGGGCGCTTCA[A/G]GAGCCCCCTCCTGAG	10612
rs548406391	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475260	AGGAGCTTTGGGAAC[C/T]GCCTCAACCTCTTAT	10612
rs548423926	in-del	-/GCC	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6452942	GACTAATGACCAAGT[-/GCC]ACCACCCTCCGCCCT	10612
rs548458216	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450157	GTCTCAAACACTCTC[C/G]TCCTCCTCTGCCTTC	10612
rs548589169	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461731	CAATATCCCCTTCCT[A/G]TTTGTCAAGTGTACC	10612
rs548663775	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449738	ATGAGTCACTCTTGA[C/T]TCCAATTTCTTCTCT	10612
rs548814484	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452610	TAATGTGGACCTTCT[A/C]CTAAGCTCTTCTCTG	10612
rs548943430	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455311	TGTGACTTGTTAGTA[A/T]GTGACAGAGCTAGGA	10612
rs548986424	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464560	TCTTTCTCTTTCACT[A/G]TACTGTTAGCTCTTT	10612
rs549047850	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458449	CATCTCATCTGCCAG[C/T]AGGTATAATGGCCTT	10612
rs549079408	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6458705	GTGCCTACCCTTAAA[A/G]TACTTCCCATCTACA	10612
rs549133149	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453116	ACTGCATCTGTTTTG[C/T]TTGCTGCTGCACTTG	10612
rs549212232	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460230	ATGTCCACTGAATTT[A/G]GCAAATGTGAGGGTA	10612
rs549265561	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6468295	TCTATGTATGCTAAG[C/T]ACAATGTGTCTCTCT	10612
rs549277263	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454397	GTCTCAAAAAAAAAA[A/C]AAAAAACTATGAGGA	10612
rs549298449	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6466059	TGTGACATAGTGCCT[A/G]TTGAGTGCATGGTAC	10612
rs549417672	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472347	TCCCATCTTGTACTA[A/C]CTCGATGATTTGACT	10612
rs549478722	snp	A/G	0.00022291	0.0105549	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465707	CCATGGCGCCCACAG[A/G]TGGCTCCCGCCACTC	10612
rs550072003	snp	A/T	0.00540606	0.0517089	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448848	CCAGTCACCAAAGCA[A/T]GAACCGAATAAATAA	10612
rs550085104	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6461030	CTTGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA	10612
rs550187348	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473159	CCAGGATCTGAAGCC[A/G]ATTGCAGAAGGGAGG	10612
rs550262661	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460322	TTGAGTGAAGGGGAG[C/T]TTGAAAGTTCCAATG	10612
rs550319754	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6469312	GGACCAATAGCTCCT[A/C]CCCCACTCCTCCCCT	10612
rs550337750	snp	A/G	0.00074209	0.0192482	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457370	GCAGTGCTTGCTCCA[A/G]GTCCTCGAACGCTGC	10612
rs550357357	snp	G/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6469155	GCTGAAGCCTCTGTC[G/T]GGTGAAGGGAAAGGC	10612
rs550517273	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6469559	TCTCCTTTCTCATAC[G/T]GCCTTCTGCTATCCC	10612
rs550727346	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6463752	TTCTGGATTATAAGA[A/T]TCAGGGCATGGTTGG	10612
rs550812685	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6471588	GCTGTGAAATAGAGA[C/T]ACAAAGCTGAATCAG	10612
rs551272257	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464974	CTTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA	10612
rs551481803	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471775	AAGAAGGCTTCCAGA[A/G]GAAGGGGTATTTGAG	10612
rs551551650	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472150	AAGTTAGGAGATCTA[A/G]GATCTAGTCCTAATG	10612
rs551613146	snp	A/G/T	4.94176e-05	0.00497059	synonymous-codon, missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465614	TGGGGCACTGGTACC[A/G/T]ATCCAGGCAGATGCT	10612
rs551881137	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6470094	AAAAAGCAAAGGAAA[A/C]CTTTGGTAGTGGTGA	10612
rs551947265	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467996	CTGATTTGAGAAATA[A/T]TCATTGGCCGAGCAA	10612
rs552580251	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457215	GGGGAATGGGGAGCT[A/G]GTGTGGAAGACAGAG	10612
rs552610392	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461435	TTGCCCCCACTTCCA[A/G]TTGTGGACATCTTTC	10612
rs552795993	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6472421	AGTTGCCTCCCCTCC[A/T]CACTCCCCCTGCCCC	10612
rs552932799	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475287	TTATCCACCTGAGTT[C/T]AGCACATAGCACAAG	10612
rs553162698	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475904	CCGTGTTAGCCAGGA[C/T]GGTCTTGATCTCCTG	10612
rs553164222	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454673	CCTGTGCTGCACAGG[A/G]CCTCTCCATTCCTCT	10612
rs553188263	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474596	AATTCTCAGAATCAT[C/T]GCCTTGTGCAAAAAG	10612
rs553236952	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450359	ACACAGAATACATTT[G/T]CTTTGTGCATCACTG	10612
rs553294152	in-del	-/CCCT	0.00237388	0.0343701	intron-variant	TRIM3	GRCh38.p7	11:6452943	ACTAATGACCAAGTA[-/CCCT]CCACCCTCCGCCCTA	10612
rs553531313	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469557	ACTCTCCTTTCTCAT[A/G]CTGCCTTCTGCTATC	10612
rs553717033	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457543	TTTCCCTTCTCCCTG[A/G]GGAACCTACTGCTGC	10612
rs553853555	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448345	CATTCCCTCACCCCC[C/T]CAACCCCACAATCCT	10612
rs554003639	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472483	TTAAGTCACCTGTGA[C/T]ACTCTATGAACGCTC	10612
rs554003885	snp	C/T	0.00478085	0.0486577	intron-variant	TRIM3	GRCh38.p7	11:6465479	CTACAGGTTTACACA[C/T]GCTCCCTCACCCTCC	10612
rs554066427	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465875	ACTGGAAGGATCAGG[G/T]TGATGTGACCTCTGA	10612
rs554127860	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6466231	AACTGCCTGAAACTG[C/T]ACTCTTTTTCACACC	10612
rs554194269	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470713	GATGTTGGTGCAGAG[A/G]TGGTTCCTGAAGCCA	10612
rs554395941	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473519	GCGTTCAGCACCCTC[C/T]GCCAACACACACAAG	10612
rs554457480	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467596	CATAATGAGACCAAT[A/G]TCTACAAAAAAATTA	10612
rs554679964	snp	G/T	0.00159617	0.0282053	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448400	AAGGACTTGCCTACT[G/T]CTGTAGGGCCTGGGG	10612
rs554916152	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6454718	GGTAGGAGTAAAGGA[C/T]GACTGGACAGAACTG	10612
rs554926548	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461234	TGTGACTTACTTTTC[C/T]TTGCAGTCCTCTCAA	10612
rs554935853	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448368	ACAATCCTTCCCAGC[C/T]CCAGGGCAGATAGGC	10612
rs554989449	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455155	ACAGCCTCCACCTGG[A/C]CGATGATATTTTTAA	10612
rs554989688	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468204	CAATTATGACTTAGC[G/T]TTCTCATTTTAGCAA	10612
rs555053773	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451564	GTCATTCAACAAGCA[C/T]TTACTGACAAAATCA	10612
rs555136437	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474808	CAGCTAGAAAGTGGC[A/G]GAACCTGGAGTTGAG	10612
rs555243090	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6469271	CCCAGACTGTCACAC[-/A]GGGGCGGGGATTGGG	10612
rs555339946	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464724	AAGCACGGTAGCTCA[C/T]GCCTGTAATCCCAGC	10612
rs555403318	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458686	GACAAAAAGATAAAG[C/T]ACAGTGCCTACCCTT	10612
rs555476137	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471863	AGAAACAGAAACATG[A/G]GAAACTAAGAAATAT	10612
rs555731520	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453896	TCAGGGAGCCCAGCC[C/T]ATGCCAGCCCTAAGG	10612
rs556173636	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6452665	CTGCAGTGGTCCCCT[A/G]TGGCAGGACAGCACT	10612
rs556193238	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453519	CCAAAATAAAACAAA[A/G]CAAAACCAGACAAAA	10612
rs556254794	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6453974	GCTCCTAGCAGTGGC[A/G]ACATAGAGGGCAGGT	10612
rs556276373	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465728	CCCGCCACTCACACC[A/G]GCCTCTGTATGGAGA	10612
rs556337794	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459856	AGAAAGAGGAGTAGC[C/T]ATAGGAAAGTTCAGC	10612
rs556397653	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471223	ATGAGTTACACAGTT[A/G]TGAATGGAGGTAACC	10612
rs556451922	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465419	CATTTCCTGCAGGTT[A/G]GGGTTCACCTGCTCT	10612
rs556591351	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6455950	ATTCACTGCTCTTAA[C/G]GAACGGTACTATCTG	10612
rs556673662	snp	C/T	0.00318978	0.0398085	intron-variant	TRIM3	GRCh38.p7	11:6462046	TCCTGTCTACTTCTT[C/T]CTCAAGGCCTTTGCA	10612
rs556725006	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450443	TAAATGTGTATTGTT[G/T]GAGTGAATGATCTCA	10612
rs556776193	snp	A/G/T	3.34696e-05	0.00409071	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451457	GAGCAGAGGAGCAAG[A/G/T]GGAGGGAGCAGGTAG	10612
rs556905829	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468647	GATTTGGCTGTGGTG[A/G]GGTGGCAGGGGCAGA	10612
rs556967125	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6462614	GCATCTCACTATGTT[A/G]TTTCCCAAGCTACTC	10612
rs557449284	snp	C/G	8.43576e-05	0.00649397	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451473	GGAGGGAGCAGGTAG[C/G]AGGGGAGACACTGTG	10612
rs557450092	snp	A/G	1.67565e-05	0.00289447	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456913	CTCTCGCATGTGCTT[A/G]CGCACCAGCAACACC	10612
rs557640250	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457918	CTCCCCACCTGCCCT[C/G]CCTGCCCCTCACCTT	10612
rs557701917	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452157	AGAGGAGAAAGTATA[C/T]AAGAATTAGTCCATT	10612
rs557789973	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464214	TGGTCTGGCCTCCAC[A/C]TACCTCTCCAGCTTC	10612
rs557926167	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6459028	TACTTATTATTAATA[C/T]AAGGAATGATAGAAA	10612
rs557990346	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457981	AGAGCAGTACCCTGT[C/G]ACCCAGCCACTCGGC	10612
rs558197421	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474622	AAAAGCAGCCCCAAG[G/T]GGAAAATAATTGTAA	10612
rs558258979	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6467275	AAAAATGGTATGGGT[A/G]AGGGTGAGAAACAAC	10612
rs558571664	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6454531	TCTCAACTTTTATGC[C/T]AGGAAGCATTCCCAG	10612
rs558635592	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6467318	AGGGAAATCATTCTA[A/G]GCTGAAGAAACAGCA	10612
rs559128250	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475402	GAACTGGAGTCTAGA[C/T]GACACTATCTTAAGC	10612
rs559145813	snp	A/C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454855	GATGACATGAGTACT[A/C/T]AAGCAGGGTCAGGAA	10612
rs559190435	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468244	CATGAATAGAGACAG[C/T]GAAAGCTGAGGTGGA	10612
rs559192373	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475821	GAGTAGCTGGGACTA[C/T]AGGACTACAGGCGCC	10612
rs559253620	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468694	CTGAAGAGTAAATGG[A/G]AGATGAAGTTAACAC	10612
rs559420498	snp	C/G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455320	TTAGTATGTGACAGA[C/G/T]CTAGGATTCAAGCTC	10612
rs559429260	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475118	AAATCCTGAAAAATT[C/T]TGGTTTCCTTGGCCA	10612
rs559858297	snp	C/T	0.00358779	0.0422022	intron-variant	TRIM3	GRCh38.p7	11:6468313	AATGTGTCTCTCTGA[C/T]GTCCAGGTAGAGCTG	10612
rs559959376	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476151	AGGCCCTAAGCACTG[C/T]GGGCAGGGACCGTGT	10612
rs560263913	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464495	TATTTGCAGCACTTA[C/T]TAAAAGTTATATTTA	10612
rs560284095	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461866	CCTGTATATATATAT[A/T]TTTAAAAACTCCAAT	10612
rs560292219	snp	A/G	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6458812	CAGGCCCAACACCCC[A/G]TTGGTCACCTGTTAT	10612
rs560508865	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6460539	GTCAGTCTCTGAATG[A/G]AGGGAAGGAGGAAAG	10612
rs560531646	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472747	AAGTGAATAAAGTCC[C/G]AAGAAGAGAGACCTC	10612
rs560683827	snp	A/G	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6472241	ATTTGTAAATTGGGA[A/G]AAGAGGGATGTTTTC	10612
rs560723678	snp	A/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6471994	ATCTAAATAAATAAA[A/T]AAATAAAAGGCACCA	10612
rs560934635	in-del	-/T	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6464573	CTATACTGTTAGCTC[-/T]TTAAGAGTAAGCATT	10612
rs560993523	snp	A/C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459384	AGCTCCTCTTCACCC[A/C/T]CTCTGTGTGGGGAGT	10612
rs560998585	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6462350	CTCTGCAGTGAAAAC[C/T]GGATTCAGATCTCAG	10612
rs561053378	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453708	ATAATATATACAAAT[C/G]AAATTATTAATTCAG	10612
rs561117925	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454228	TACTAAAAATAAAAA[G/T]AAAATAAAATAAATT	10612
rs561274586	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454910	GTAAGGATCTTCAGC[A/G]AAAAGTTTTGCTACC	10612
rs561329624	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466860	CTTATAAGCTATGCT[A/G]TAATGTTCTTGTTAC	10612
rs561414277	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472828	CACTGGAGGCATACA[A/G]GCCCAAGGAGGCAGG	10612

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