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

TRIM4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs561952525	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99907258	AAGTAGCTGAGATTA[C/T]AGGTATGTGCCACCA	89122
rs561966658	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921534	AAGACTTACACAACC[A/G]TGTCTCTGTTGGGCT	89122
rs562094959	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99889998	TGTGTGTGGGCATGA[A/G]TGTGTGAACATATGC	89122
rs562137060	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911817	GAAAACATGTACCCA[C/T]AAATAGACCTGTACA	89122
rs562294651	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890928	GTCTTTACTGAAAAT[A/C]TGGGAGAAAATATAT	89122
rs562312934	snp	A/C	0.000399281	0.0141238	splice-donor-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919008	GCGACGGCCAGCTCA[A/C]CCGGTAGCTCTCGAA	89122
rs562324893	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899391	TGTCCAGCTGGCCAT[C/T]CCTGGACTGCCCTGC	89122
rs562484991	snp	A/G	1.64743e-05	0.00287	missense	TRIM4	GRCh38.p7	7:99892410	GCAGCACTCCAATAA[A/G]TCGCCCAGATGCCCA	89122
rs562555693	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905819	GAAGCCAGTACGAAA[A/G]AGTGCGTCCTGAAAG	89122
rs562886451	snp	A/T			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919710	CTATAGAGACCCAGA[A/T]ATGCCTGTGGAAAGC	89122
rs562935543	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99910764	TGTAATTTAAAAACC[C/T]GAGTAAGTTATTAAA	89122
rs562941358	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918725	CTATTGGACAGCAGC[A/G]GCACACACCCTCTCA	89122
rs562978464	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918200	CACCTGAAACGTGGA[C/T]ATTCCAAACTGCTAT	89122
rs563148677	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919572	AAAAAGAACGCACGG[A/G]CGTTGCCCGGCCTGA	89122
rs563316385	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99904681	AATTGTTCATTTTTT[A/T]AAAAAAACTGGTTAA	89122
rs563479984	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896944	GAGCTTGTGGCACAG[A/G]CAAGGGTGTACCACT	89122
rs563547844	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901614	TGTGGAGCAGCACCC[A/G]GTCAAGGGCTAAATA	89122
rs563588351	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908960	AAATTTCCATTACTC[C/G]TTTATTTATACCTAC	89122
rs563729607	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99917257	CTCATCCACTTATGT[C/T]CAGATTCTAAAACAA	89122
rs563783014	snp	A/C	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99894669	AAGACTCCATCCCCC[A/C]CCCAAAAAAAAAAAG	89122
rs563952107	snp	A/G	0.000159949	0.00894141	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919339	CTCGATGGACACCGG[A/G]TCCTGGAAATAGTCC	89122
rs564032232	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906277	GTTCTATTTTTTTGA[C/T]TTGGATAGTAGTTAC	89122
rs564112968	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99914965	CAGGTGCCCACCGCC[A/G]CACCTAGCTGATTTT	89122
rs564122658	snp	A/C			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918464	CAGCTACTCGGGAGG[A/C]TGAGGCAGGAGAACT	89122
rs564170776	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918882	TGCTTAACTTCTTTG[A/G]GTTTCAGGGGCTTTT	89122
rs564291431	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891028	CACATGACTTATATA[A/C]ACAGAGAAAAGCAAT	89122
rs564328498	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898101	GAGCCATGTCTATAT[C/T]TGGCATGATAAGTCT	89122
rs564337301	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895563	AATGGGATCAAGTTG[A/C]TTGATAATATTATTC	89122
rs564483782	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99896312	AGTGGCCAACTCAGA[G/T]ATCTGCTCCTTTTCT	89122
rs564484836	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902983	GTGTCTGTCTCTCCA[A/G]TGTGCTTACGAACTC	89122
rs564523164	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99902360	TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCGAG	89122
rs564964561	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914654	CAGAGACCTTCTTCC[C/T]ACCCCATAAACATAT	89122
rs564996599	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916593	AAGACTCCTCTCTCT[C/G]TCACCCACCAAGTCT	89122
rs565029901	snp	A/G	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99894596	CACTTGAACCTGGGA[A/G]GTGGAGGTTGCAGTA	89122
rs565062091	snp	G/T	0.000282521	0.0118819	missense	TRIM4	GRCh38.p7	7:99909641	GCCACGAGATTACGC[G/T]GAGACTTAAGAAGTT	89122
rs565063772	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896943	TGAGCTTGTGGCACA[A/G]GCAAGGGTGTACCAC	89122
rs565191049	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907915	ACATGAATTATTTCA[C/G]CAAAAAGAAAAAGCA	89122
rs565312699	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99893754	AGGTTCTTTTCCTCC[C/T]CTCCACTCCCATTGC	89122
rs565351244	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900812	AAGTGTAATGTCAAC[C/T]TCGTCTTTGTTCCAC	89122
rs565369885	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99901114	CCCACAGGTCACTGA[A/T]GCTCTTTGTGTTTTT	89122
rs565434724	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99900095	CCAGCCAGTGTATAA[G/T]ATTTAATATAAGGAA	89122
rs565621564	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916025	GAATAACAGAATCCA[C/T]CTAATAGGATGTCTA	89122
rs565805248	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99899715	TCCAAAGGAACAGAA[C/T]CAAAAGGATATATAT	89122
rs565874902	snp	C/T	0	0	intron-variant	TRIM4	GRCh38.p7	7:99895595	AGTCTACTATATCCC[C/T]GCTGATTTATTGCCT	89122
rs565951829	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901830	TGATCAGAACTCTGC[C/T]AAACAACTAGGAAGC	89122
rs566172816	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914712	TCCCACAGTTCCTCA[A/G]ATGGCAGACTCTGCA	89122
rs566298988	snp	C/G	0.00358779	0.0422022	intron-variant	TRIM4	GRCh38.p7	7:99897936	CTCACCTGTTGCCCA[C/G]AGATGGGGTGCAGCA	89122
rs566300714	in-del	-/TAAT	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99895610	TGCTGATTTATTGCC[-/TAAT]TATTCTAAAAATTAT	89122
rs566324521	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893891	TTTGAGGACTTTTTT[A/T]AAAAAAAATCAGGAA	89122
rs566633159	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921263	AGACACGAGCTGGTC[A/C]TTCTTTCACTGTCTC	89122
rs566680115	snp	C/G/T			intron-variant	TRIM4	GRCh38.p7	7:99895362	TGATATTTAGGGGGG[C/G/T]TTCTAAGGATATTTT	89122
rs566771524	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99907392	TGGGATTACAGGCGT[A/G]AGCCACTGCACCCGG	89122
rs566776265	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920465	TATTTGCTGAAGCTC[A/G]GCCGTGATTGGCTGA	89122
rs566794310	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919711	TATAGAGACCCAGAA[A/G]TGCCTGTGGAAAGCT	89122
rs566935282	snp	A/C	0.000399281	0.0141238	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919200	TCTCAGTCAGCCTGG[A/C]CAGGGCCCAGTTGGG	89122
rs567054180	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891352	GTGATGAGAGTCATA[A/T]GCAACAGCATATGAA	89122
rs567061396	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912856	GCACAATACCATCTG[C/T]GCTATTCTGTTTCTA	89122
rs567070733	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99899024	CTCAGGGAAGTTGCA[A/G]AGAATGACGTGATAA	89122
rs567105341	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905882	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	89122
rs567143847	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905124	ATACCTTTAGGAAGA[C/G]GGAAGGGGTGCTGAC	89122
rs567336044	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920237	AAATTTAATAGAAGC[C/T]ATTTGCACAAAGAAC	89122
rs567408132	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891006	TACAAACTTTCTACA[A/G]TAAGTACACATGACT	89122
rs567429161	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919767	AGCCGGACGTTGTGG[A/T]CCCTGGGGGAGCCAA	89122
rs567446367	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99908276	TGTTTTATTGTTTAA[C/T]AATTATAAATGTACA	89122
rs567498523	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915648	AACTTGGGGTGGGGA[C/T]GGAATGAAAGGTGGT	89122
rs567533431	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914963	TACAGGTGCCCACCG[C/T]CGCACCTAGCTGATT	89122
rs567679994	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99905208	TGACAAATCTAAGTA[C/T]TGGTGAGGATACACA	89122
rs567715778	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890529	ATACACCATGGAATA[C/G]TATGCAGCCATAAAA	89122
rs567716292	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99913055	ATTAGTTCCTTCAAA[C/T]AGGACCAAGTTTTTG	89122
rs567751603	snp	A/G	0	0	intron-variant	TRIM4	GRCh38.p7	7:99897129	TGTCCTGGAACCCTA[A/G]GTCCTGGGACCCCGT	89122
rs567875757	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899604	TTTCATCTCTCCTCT[C/G]CCAATCTTCACACTA	89122
rs567875893	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892041	ATACCAAACGGTACC[G/T]TTAGGGAGACCCAGA	89122
rs567903892	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906616	AAACAAAGGGGTAAA[C/T]ATAAAGGAGCCAAGC	89122
rs567913676	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906665	GAGAAAAGAGCTAGA[A/G]AAGAAACCCAAGGAC	89122
rs567976253	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99903038	TTTTTGTATCACTAG[C/G]ACCTTGTAACAGTGC	89122
rs568032408	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904204	ACTTAAAGACATAGA[C/T]GTGAAAATTCTAAGT	89122
rs568069156	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912067	TTGTGTTTGAAAAAA[A/T]ATCAGAACGGTGGTT	89122
rs568215134	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915724	ATATCAGGGAATTCC[A/G]CCCAGTGACCTGGCT	89122
rs568308106	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99903391	CGGTCAAAGGTTCTT[A/G]GCCCAAAGTTCAGAT	89122
rs568582996	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914639	TTGGTCCTCCAGGTG[C/T]AGAGACCTTCTTCCT	89122
rs568597875	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99897131	TCCTGGAACCCTAAG[A/T]CCTGGGACCCCGTGA	89122
rs568613435	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99895661	TGCAAACGTAATTGT[C/G]AATTTGTGTATTTCT	89122
rs568626132	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM4	GRCh38.p7	7:99910709	ACTAGAAATTTTATG[C/T]ATTTTTGCTTTAATT	89122
rs568666524	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917781	ACTTACTGCATATCA[A/T]TTCTGCTGGAGACCA	89122
rs568808557	in-del	-/T	0.0126979	0.078662	intron-variant	TRIM4	GRCh38.p7	7:99894974	TTCTGATCATTTTGA[-/T]TTAAAGGTGTGTCAA	89122
rs569330319	snp	C/G	0.00159617	0.0282053	intron-variant	TRIM4	GRCh38.p7	7:99902040	CTCAGGCAGAGGGTA[C/G]GGCAATCATAGGCTG	89122
rs569338254	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909742	TTGTTTTTTTTTTTT[G/T]TTTTTTTTGAGACAA	89122
rs569384712	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99917518	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	89122
rs569424445	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897217	CCTCTCAGCATGTCT[A/G]ATGGTCACTACCAAG	89122
rs569459512	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904259	CGTGTATTTAAAAAA[C/T]ACAGCTCCTCCAAAA	89122
rs569583297	snp	A/T	0.000798403	0.0199641	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919121	TCGCAGAAGAGCCGC[A/T]GCGGCTCCCAGTGGC	89122
rs569613953	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909196	TCTGTTTCTTTCCAC[A/G]ATGCCATGGGCCCAA	89122
rs569622841	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902617	AGAGCATGTACCTGC[C/T]TTGGTGCCTCCCTGG	89122
rs569732313	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99894007	GATATAAACTACATC[A/G]ATTTTCAAATATTAA	89122
rs569769018	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99896564	TATGTCTCATTCACC[A/G]GCTCCAGGTTTCTTC	89122
rs570089281	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99901061	CCTCTCTTTCAGGGA[C/T]GCCAATCACCATAGA	89122
rs570185791	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99902770	CACCTTAGCTCATGC[C/T]GCTGCTTCTGCTTGA	89122
rs570222951	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99909999	AGCCTCCCAAAGTGC[C/T]GGGATTACAGCCATG	89122
rs570410250	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919573	AAAAGAACGCACGGA[C/T]GTTGCCCGGCCTGAG	89122
rs570577001	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TRIM4	GRCh38.p7	7:99890293	GGGGAGGAGGGGAGG[A/G]GGAGTTAGGGAAGAT	89122
rs570597683	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99903371	GTAGCCAAGACCTCC[A/T]CTCCCGGTCAAAGGT	89122
rs571098437	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99904903	CAGGCATGATGGCGG[C/G]TGTCTGTAATCCCAG	89122
rs571240069	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890827	CCCCTGTGACATGTA[A/G]TTGATCTATAGAACA	89122
rs571304890	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99893189	GAAGAATCACTTAAA[C/T]CCAGAAGGCGGAGGT	89122
rs571311915	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915006	GTAAAGACAGGGTTT[C/T]ACCATGTTGGCCAGG	89122
rs571333262	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906763	AGGCAGGAAAATTAC[C/T]TGAGCCCAGCAGCTT	89122
rs571387857	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99901154	TTTATTCTGTGTATG[C/T]TTCATTTTTTTGTAG	89122
rs571417261	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99901678	CGCTACTCAGTGCCC[A/G]TGAACTACGAGTTTT	89122
rs571420461	snp	A/T	0.0111196	0.0737302	intron-variant	TRIM4	GRCh38.p7	7:99913661	GGGCAACACAGTGAG[A/T]CTCCATCTCAAATAA	89122
rs571577018	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99915763	CCTACGAAGTCAACC[C/T]TGTGACATTCAGCCC	89122
rs571725786	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921153	GGTTCATTCAGAGAA[G/T]TGGAATCACTATGTT	89122
rs571825933	snp	C/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99893214	GGAGGTTGTAGTGAC[C/G]CGAGATCGTGCCACT	89122
rs571964222	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99910521	AGCCATAAGACAATA[C/T]GTATTGTACAATTCT	89122
rs571966638	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906072	ATAGCTTGTACCCGG[A/G]AGGCAGAGGTTGCAG	89122
rs572052692	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907211	CAATCTCTGTCTCCC[A/G]GGTTCAAGTGATTCT	89122
rs572061550	snp	A/T	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99893623	TCTAAGGTGTCAGAG[A/T]CCCCTCCACCTGAAC	89122
rs572113308	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915089	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	89122
rs572342404	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99894384	AGAAAATCATCTGGG[G/T]ACCAGGCGCGGTGGC	89122
rs572594804	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914583	AAGCTGACCGCTGCC[A/T]ACATCTCGTTTCACA	89122
rs572705819	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919871	TTTAAGTTTTAGAGT[A/C]CCAGGAGTTCTGGGC	89122
rs572746514	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99906117	TCCACTGCACTCCAG[A/C]CTCGGCCACACAGCA	89122
rs572746774	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99898580	GTCCCATTGAGACAC[C/T]ATTCTTACTAACTGG	89122
rs572781651	in-del	-/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99900743	ACTCTAGGTTAACAG[-/T]TTTTTTCTTTCAGGA	89122
rs572876019	snp	A/G	6.66867e-05	0.00577398	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919394	TCCTGGATGTCCTCA[A/G]CTTCCATGCTGCTTC	89122
rs573073825	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913333	GGCAGGAGCGCAACA[C/G]CAAGCATTTCAATCT	89122
rs573273893	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918497	TTGAACCCCGGAGGA[A/G]GAGGTTGCAGTGAGC	89122
rs573332102	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902549	TTCGTGCCCGGCCTA[C/T]AACATGGTTCTTAAT	89122
rs573357785	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99911550	TTTAAATTCTTCCCC[A/G]GAAAACTAACAATTA	89122
rs573389579	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99896400	GAGGATCAAGGCCCT[C/T]TGATTCGGGTTAAAT	89122
rs573394948	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99910564	ATAAACGTGTCTATG[C/T]GCATACGTGTTTATC	89122
rs573494233	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99892981	AGACCAGGCGCAGTG[A/G]CTCATGCCTGTAATC	89122
rs573563115	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899312	GGTCCCAGGTGGAGA[C/T]TGCTAAATGAAAATG	89122
rs573697722	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917135	CTCAGTGATCACTCC[A/G]ACCTCAGACCTTCTG	89122
rs573719603	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99913922	GCCTTGCTTATTTCC[C/T]GGATCAAGGCTTCCT	89122
rs573722400	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900114	TAATATAAGGAACTG[A/G]CTTGTGTGATTATTG	89122
rs573765202	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920622	TTAACAGATTTTTCA[C/T]TCTTTTTATGTCCCA	89122
rs573834932	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99914254	CCTCGAACTCCTGAG[G/T]GCAAGTGATCCTCTA	89122
rs573855786	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99906226	GGGAAGAGGTACTGA[C/T]TGGGGACATGAGGAA	89122
rs574016996	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99904570	ATTAATTGTAACAAA[G/T]GAACTATATTAACAC	89122
rs574053769	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99912479	AGGTTTCAGTGAGCC[A/G]AGATCACACCACTGC	89122
rs574075331	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890950	AAAATATATTGAAAT[A/G]TTAGTAGTGCATAAC	89122
rs574113536	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99897903	AATGGCTTCCCCTTT[C/T]TTGTACCCACTAAAC	89122
rs574338332	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919260	GACATTCGGGGCAGG[A/G]GAACGGGCCGCCGCC	89122
rs574721026	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99895430	CATACTCTGAATGAT[C/T]GGAATCCTTTGAATT	89122
rs574772627	snp	G/T	0.02016	0.0983543	intron-variant	TRIM4	GRCh38.p7	7:99909135	TTAGGAGTGTGAGGG[G/T]GTGTGTGTGTGTGTG	89122
rs574817151	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916462	CTTCACACTCAGTAC[A/C]TTCCACAAGCATGGG	89122
rs574835825	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99906000	AAATAGAAAAATTAG[C/T]CAGGTGTGGTGGCAC	89122
rs574877214	in-del	-/A	0.00478085	0.0486577	intron-variant	TRIM4	GRCh38.p7	7:99897584	ACTAAAAAAAAGAAC[-/A]AAAAGATTTCTCAAG	89122
rs575082225	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99909462	CATCCAAGACTCTAC[A/G]TGAACTGCAAAACCC	89122
rs575184410	snp	C/G	0.000399281	0.0141238	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919285	GCCGCCCGGCGCCCA[C/G]TTGCGGTGCAGGCAG	89122
rs575190968	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921042	TGTCTTTATTCCTGC[C/T]ATACCAGAGATGACC	89122
rs575444934	snp	A/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99904682	ATTGTTCATTTTTTT[A/T]AAAAAACTGGTTAAT	89122
rs575505013	in-del	-/C	3.29557e-05	0.00405916	frameshift-variant, intron-variant	TRIM4	GRCh38.p7	7:99916729	ATGGTACAAGAGCAG[-/C]CTAATTAGTCTTCTC	89122
rs575677571	snp	C/T	0.00517822	0.0506191	intron-variant	TRIM4	GRCh38.p7	7:99895493	TTGGAAAATGTTTCA[C/T]GTACACTGAAAAAAA	89122
rs575789086	snp	A/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918037	CCAAATTCAAATGTT[A/G]CAGGATTTTCCCAAC	89122
rs575846554	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99896522	ACTGCTCCTGGACCA[C/G]CCAGCATATAAGTCC	89122
rs575911770	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99903473	AGACCCCCATTAGGG[C/T]GTGCCCAGACTGACC	89122
rs576051537	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM4	GRCh38.p7	7:99901435	TTTCCTATCTTTTTG[C/T]ATGCATATTTGACTG	89122
rs576059341	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900709	TTGTTTTTGAAGGAT[A/T]TTTTTTGCCAGTTCT	89122
rs576083704	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99893479	TTCACGGGTTCCAGT[G/T]GTTTATGGGGCATCT	89122
rs576097126	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM4	GRCh38.p7	7:99895186	AGTTTCTTCTTTCCA[A/G]TATAGCACTATACAC	89122
rs576183123	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913777	AACACAAGTGTAATA[A/G]AAGAGCATACTTTTA	89122
rs576268361	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99916155	TTTAAGGGCTATGTT[A/C]CCCTTTCATACCCAT	89122
rs576304653	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99915191	CTGTCTGCTATCTAC[C/T]TCCCACCCTCAGCCC	89122
rs576597156	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907862	TCTTCATTCACGTGA[C/T]ATGGAGGAAAGAGAG	89122
rs576660959	snp	A/C	1.64757e-05	0.00287012	missense	TRIM4	GRCh38.p7	7:99892379	TCCAGGGAAGCCTAT[A/C]AAGGGCCAATAGCCA	89122
rs576923805	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917956	GCCAGTATGGCTGAA[A/G]CAGAGTAAGGTAAAG	89122
rs577078878	snp	A/T	2.82466e-05	0.00375799	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919178	CCCAGGCGCCGGCGC[A/T]GCGTCTTCTCAGTCA	89122
rs577682344	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921487	CACCGTTTCAAGTAT[A/G]AAACTGGAGGGATGC	89122
rs577727331	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99905427	ATGTTCACACATATT[C/T]CTGTTTTTAATAATA	89122
rs577759174	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99907186	GCAGTGGCACAATCT[C/T]GGCTCACTGCAATCT	89122
rs577791728	snp	A/C	0.00279162	0.0372561	intron-variant	TRIM4	GRCh38.p7	7:99917513	TCACCTGAGGTCAGG[A/C]GTTCGAGACCAGCCT	89122
rs577835177	snp	C/T	0.00199481	0.0315187	intron-variant	TRIM4	GRCh38.p7	7:99914031	CTGTAACTTCTGCAA[C/T]TGATCCAAGCTGGTA	89122
rs577840887	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99900442	CTGGGCACTCTGTGG[C/G]CCAGTCAAGTTGATG	89122
rs577961314	snp	C/G/T	1.94744e-05	0.00312039	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892124	TGTGTCCCTCAGCTG[C/G/T]ACTACAGGGAAGGAG	89122
rs577991082	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99899137	GAATAACCCTATGGT[C/G]TAAGAAGACTGTGTA	89122
rs578014398	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM4	GRCh38.p7	7:99898536	TGGTAGATGCACCTG[C/G]GGTCGTCTTCACCTG	89122
rs578075919	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920675	TAATAATTTTTCTCA[C/G]TAAGTAGTATGATTA	89122
rs745362030	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897730	TGTGCAAGGGGACAA[C/T]CATCCTCTTATAGAA	89122
rs745386915	in-del	-/GTCCTAGAAATTCT	0.000239071	0.0109306	intron-variant	TRIM4	GRCh38.p7	7:99903198	TCTAAGGAGCCCCAA[-/GTCCTAGAAATTCT]GCTCACCTTGGAATC	89122
rs745388652	snp	C/T	6.58989e-05	0.00573978	missense	TRIM4	GRCh38.p7	7:99908661	GAAGCGATAGTTTGA[C/T]TGAGTTTTAACGTGT	89122
rs745391513	snp	A/G	1.64977e-05	0.00287203	synonymous-codon	TRIM4	GRCh38.p7	7:99892264	AAGAAAAGGTGTGCA[A/G]GTGCACTCCGTCCAC	89122
rs745454279	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99908016	AAAGGTAAAGATTAA[C/T]TCAAAGGAGGGGCTT	89122
rs745466857	snp	C/T	3.29679e-05	0.00405991	intron-variant	TRIM4	GRCh38.p7	7:99916699	AATTCAGGTCTTTAT[C/T]ACCTCCTGCTTAAAA	89122
rs745533816	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99894570	TACTTGGGAGGCTGA[A/G]GCAGGAGAATCACTT	89122
rs745590894	in-del	-/A			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890460	ATAGCAAAGACATGG[-/A]AATCAACCTAAATGC	89122
rs745620602	snp	A/G/T	0.000128562	0.00801669	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919360	GAAATAGTCCAGGCA[A/G/T]ATGGGGCAGGTCAAC	89122
rs745625537	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99896668	TGGAGAAAATTCCAC[G/T]AGTGCCAAGACAATG	89122
rs745676013	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916910	AAGGCCCTGCCTTTT[C/T]CTTCAAGCTCATGGC	89122
rs745851317	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99898826	CCCTATTACTCTCAC[A/T]TTATAACCGGGGTTA	89122
rs745906777	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99914349	TTTTTGTAGAGATGG[C/G]ATCTCACAGTTGCCT	89122
rs745912918	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99912771	GATGTATGCTTGAAA[G/T]TTTCATGGTAAAATG	89122
rs745931126	snp	C/T	6.60557e-05	0.0057466	missense	TRIM4	GRCh38.p7	7:99908793	GTGCTGATTCTCATT[C/T]GCTGACTCTTTATCT	89122
rs746150245	snp	A/G	1.78188e-05	0.00298481	intron-variant	TRIM4	GRCh38.p7	7:99909523	TGTCCCAGACCAAAA[A/G]GACCTCAGGAGCAAG	89122
rs746213386	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890926	AAGTCTTTACTGAAA[A/G]TCTGGGAGAAAATAT	89122
rs746233672	snp	C/T	2.19022e-05	0.00330917	intron-variant	TRIM4	GRCh38.p7	7:99902205	CAACTCGTTTATTTA[C/T]TCCATTTTGGCTAGA	89122
rs746266418	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902537	CAGACATGAGCCTTC[A/G]TGCCCGGCCTACAAC	89122
rs746326450	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915455	CTATTTCTCTTTCTC[C/T]TTTCTCTTTTTCTCC	89122
rs746436084	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901507	TTTGTTTATTTCTAC[C/T]AATTTTCTAGGGCTT	89122
rs746497973	snp	C/T	1.65414e-05	0.00287583	intron-variant	TRIM4	GRCh38.p7	7:99916821	TTCCCTGCCTTAAAA[C/T]CCTTTTATAACTCCC	89122
rs746501908	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99907814	ATGGTAGACAGAAAA[C/T]GTTCTTGAGAACACC	89122
rs746553111	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921043	GTCTTTATTCCTGCC[A/G]TACCAGAGATGACCT	89122
rs746561484	snp	C/G	1.64727e-05	0.00286986	missense	TRIM4	GRCh38.p7	7:99892452	ATTTTTGAACGATCA[C/G]TAATTCCCATGACGT	89122
rs746578552	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920105	TTCAGGGAATTATCT[A/G]TATCCCTTAAGTGGA	89122
rs746597075	snp	C/G	3.31428e-05	0.00407066	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919033	CTCGAAGGCCTCGTC[C/G]ATGGGTGCCATGGCG	89122
rs746668744	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919581	GCACGGACGTTGCCC[A/G]GCCTGAGCGCGCAAG	89122
rs746799872	snp	C/T	1.64746e-05	0.00287002	missense	TRIM4	GRCh38.p7	7:99908676	TTGAGTTTTAACGTG[C/T]TCTCATTCAGCTTCT	89122
rs746807948	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897501	ACCCTGATTTTATCA[C/T]TATGCACTGTATACA	89122
rs746968984	snp	C/G	1.64757e-05	0.00287012	missense	TRIM4	GRCh38.p7	7:99892386	AAGCCTATCAAGGGC[C/G]AATAGCCAGCAGCAC	89122
rs746981574	in-del	-/CT			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891827	CAACGGCAACAAAAA[-/CT]CTGTTTCTTCTACCT	89122
rs746994341	snp	G/T	1.64746e-05	0.00287002	missense	TRIM4	GRCh38.p7	7:99908760	TCAACCAGGAAGTTG[G/T]GCAGCTTTGAAAACT	89122
rs747041756	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99895183	AGAAGTTTCTTCTTT[A/C]CAATATAGCACTATA	89122
rs747088496	snp	A/G	1.66738e-05	0.00288732	missense	TRIM4	GRCh38.p7	7:99909650	TTACGCTGAGACTTA[A/G]GAAGTTTCTCCTGCC	89122
rs747105293	snp	A/G	1.7585e-05	0.00296517	intron-variant	TRIM4	GRCh38.p7	7:99909533	CAAAAGGACCTCAGG[A/G]GCAAGAAATATCCAA	89122
rs747159641	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99909354	GGTACTTCCTCTCCT[A/G]TCCCCGTATCTACAA	89122
rs747277577	in-del	-/AA			intron-variant	TRIM4	GRCh38.p7	7:99907570	CAGAGATTCTTTTAT[-/AA]GACACATATTTGGAT	89122
rs747291119	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904901	GACAGGCATGATGGC[A/G]GGTGTCTGTAATCCC	89122
rs747309716	snp	C/T	3.43914e-05	0.00414663	missense	TRIM4	GRCh38.p7	7:99892705	CTTCCTGGGAGAAGA[C/T]GAGTTTGGGATGAGC	89122
rs747314616	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901409	TATTTTCCTCCATTA[C/T]GGGTCACTGCTTTCC	89122
rs747409149	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914192	TGTCCTTCTCTCATA[C/T]AATATCCACAACGCA	89122
rs747434524	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99900084	AGCCACCACACCCAG[A/C]CAGTGTATAAGATTT	89122
rs747602136	in-del	-/AA			intron-variant	TRIM4	GRCh38.p7	7:99897585	ACTAAAAAAAAGAAC[-/AA]AAGATTTCTCAAGTC	89122
rs747656368	snp	A/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919927	GCCAGGAAGACTTGA[A/T]GGATCTGTGTTGGTA	89122
rs747665132	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899477	GCCTTTCAGACACGG[C/T]GCCATCCTTAATGAA	89122
rs747673886	snp	C/T	5.68521e-05	0.00533131	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919064	TGAGTCTGGTGCTCC[C/T]GGGACTCCCTGCACA	89122
rs747709181	snp	C/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918600	ATTGATAATTTTCAT[C/G]TCAGCTTTGAATATT	89122
rs747942576	snp	C/T	1.64727e-05	0.00286986	missense	TRIM4	GRCh38.p7	7:99892462	GATCAGTAATTCCCA[C/T]GACGTCCTCCCGACA	89122
rs747983581	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99909751	TTTTTTTTTTTTTTT[-/G]AGACAAAGTCTCACT	89122
rs748036612	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906562	AAATCTGTGGAATAC[A/G]GAGCAATAAAGGTAA	89122
rs748045334	snp	A/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918720	GGTTTCTATTGGACA[A/G]CAGCGGCACACACCC	89122
rs748052247	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921462	GCAGTAGCACCTAGT[A/G]TCCCTGCACCACCGT	89122
rs748092830	snp	A/C			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891871	TGTGTTCTCAGTTCC[A/C]ATATGGCTGCTAACA	89122
rs748132712	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	TRIM4	GRCh38.p7	7:99892538	GTAATGTTTCCCTGA[A/G]GTGAAAACGTTTTTT	89122
rs748178909	snp	C/G	1.65143e-05	0.00287348	intron-variant	TRIM4	GRCh38.p7	7:99916674	CTCTCCATCATCCCT[C/G]CCCTGAACTAATTCA	89122
rs748188638	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893855	AAATTCCCTTCCCTC[C/T]AACTCTCCATGTCTC	89122
rs748211481	snp	C/T	1.79425e-05	0.00299515	intron-variant	TRIM4	GRCh38.p7	7:99902090	TCTCAGGAATCACCG[C/T]CCTTCACTGCCTGAC	89122
rs748262536	snp	C/T			missense	TRIM4	GRCh38.p7	7:99903598	ACACTTCTTTTGGAT[C/T]CTGTGAAAAGAAGGA	89122
rs748313762	snp	C/T			synonymous-codon, intron-variant	TRIM4	GRCh38.p7	7:99916705	GGTCTTTATTACCTC[C/T]TGCTTAAAATGGTAC	89122
rs748343437	snp	C/G	0.00012279	0.00783453	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919370	AGGCAGATGGGGCAG[C/G]TCAACTCCTCCTGGA	89122
rs748364312	in-del	-/TT	3.353e-05	0.00409437	intron-variant	TRIM4	GRCh38.p7	7:99909561	CAACCACTTCTGCCA[-/TT]ACCTTCCACTGTGTG	89122
rs748486581	snp	A/G	4.97113e-05	0.00498529	synonymous-codon	TRIM4	GRCh38.p7	7:99892229	CCAAAAAAATGGCCG[A/G]AGGCGTGAGACAGAA	89122
rs748541595	in-del	-/TGT			intron-variant	TRIM4	GRCh38.p7	7:99917197	ACACACTGAAATTAA[-/TGT]TGTACACGCTTAAGT	89122
rs748642361	snp	A/C/T	5.06541e-05	0.00503239	intron-variant	TRIM4	GRCh38.p7	7:99909664	AAGAAGTTTCTCCTG[A/C/T]CAGCAGAAACACACA	89122
rs748779696	snp	C/T	1.75382e-05	0.00296121	intron-variant	TRIM4	GRCh38.p7	7:99908560	GTGAAGATGAGATCA[C/T]CCCCACTCGTAACTG	89122
rs748797738	snp	C/G	3.29598e-05	0.00405941	missense	TRIM4	GRCh38.p7	7:99903576	AACAGGAGTGCATAC[C/G]TGGTCAACACTTCTT	89122
rs748826350	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899001	CAATGCTACTGCACA[C/T]ACCTTGCCTCAGGGA	89122
rs748852814	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99905091	GAAAGGTGTACATAC[-/AT]ATATATATATATCCA	89122
rs748881573	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99911328	TTGGTGAAAAACCAA[C/G]AGAGAATGGTTTCTC	89122
rs749058299	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99905430	TTCACACATATTCCT[C/G]TTTTTAATAATAGAA	89122
rs749114697	snp	A/C			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919734	GGAAAGCTACAGAGG[A/C]CTTGGGCAAGGCGTT	89122
rs749135900	snp	C/T	1.64781e-05	0.00287033	missense	TRIM4	GRCh38.p7	7:99892563	TTTTTTCCCAGAACA[C/T]AGGGTAAGTGCTGAA	89122
rs749248469	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99915829	TGTTGGGCCATTGTG[-/T]TTAATCCTGAAATCC	89122
rs749293313	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99902630	GCCTTGGTGCCTCCC[G/T]GGAGATCCAATGAGT	89122
rs749294523	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99907064	GGTAGATAGATAAGT[A/C]CAGTAGTTCTCTCAG	89122
rs749345338	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915707	GATGGAGAGATGGGC[A/G]GATATCAGGGAATTC	89122
rs749355384	snp	C/T	6.349e-05	0.00563391	intron-variant	TRIM4	GRCh38.p7	7:99902195	GACAAGAAAACAACT[C/T]GTTTATTTACTCCAT	89122
rs749663373	snp	A/G	4.9476e-05	0.00497348	intron-variant	TRIM4	GRCh38.p7	7:99916690	CCCTGAACTAATTCA[A/G]GTCTTTATTACCTCC	89122
rs749678071	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892035	GGGCAGATACCAAAC[A/G]GTACCGTTAGGGAGA	89122
rs749684566	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99904771	GTACAGTGGCTCATG[A/C]CTGTAATCCCAGCAC	89122
rs749822439	in-del	-/T	1.64741e-05	0.00286998	frameshift-variant	TRIM4	GRCh38.p7	7:99908676	TTGAGTTTTAACGTG[-/T]TCTCATTCAGCTTCT	89122
rs749850405	snp	C/T	5.38189e-05	0.00518715	intron-variant	TRIM4	GRCh38.p7	7:99902105	TCCTTCACTGCCTGA[C/T]GTCTGGTGCTTTGAA	89122
rs749870184	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891032	TGACTTATATAAACA[A/G]AGAAAAGCAATCATT	89122
rs749901961	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99911046	GTAAATGGGAGGAAG[A/G]AAAATAAATTTCACC	89122
rs750116992	snp	A/G	3.29457e-05	0.00405854	missense	TRIM4	GRCh38.p7	7:99892447	GGGACATTTTTGAAC[A/G]ATCAGTAATTCCCAT	89122
rs750134898	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900768	TCAGGACTTTAAAGA[A/G]TTTGCTTACTGGCAT	89122
rs750161872	snp	G/T	1.87268e-05	0.00305991	intron-variant	TRIM4	GRCh38.p7	7:99902160	TGTTTTGTTTTTGTG[G/T]TTTTATTTTAGTTGC	89122
rs750168329	in-del	-/GCTTCCATGCT	1.65622e-05	0.00287764	frameshift-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919393	TCCTGGATGTCCTCA[-/GCTTCCATGCT]GCTTCCATGCTGCTT	89122
rs750249744	snp	C/T	1.79577e-05	0.00299642	intron-variant	TRIM4	GRCh38.p7	7:99902088	TTTCTCAGGAATCAC[C/T]GTCCTTCACTGCCTG	89122
rs750473005	snp	A/G	6.59554e-05	0.00574224	intron-variant	TRIM4	GRCh38.p7	7:99903620	AAAGAAGGAAGACAT[A/G]AGCAAATTACGAACC	89122
rs750517431	snp	C/T	1.64754e-05	0.00287009	missense	TRIM4	GRCh38.p7	7:99908650	GCTTCTTCAATGAAG[C/T]GATAGTTTGATTGAG	89122
rs750566940	snp	A/C	1.69502e-05	0.00291115	intron-variant	TRIM4	GRCh38.p7	7:99903363	CAACTAGGGTAGCCA[A/C]GACCTCCACTCCCGG	89122
rs750679141	snp	C/T	8.87524e-05	0.00666096	missense	TRIM4	GRCh38.p7	7:99892174	AGCCTCATTTCCTAT[C/T]AGTCACTGGTGGAAT	89122
rs750728653	in-del	-/TTTTCT			intron-variant	TRIM4	GRCh38.p7	7:99895202	TATAGCACTATACAC[-/TTTTCT]TTAAGTTTTGCTTTA	89122
rs750774318	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99917573	AAAAATACAAAATTA[G/T]CTGGGCATGCTGGCA	89122
rs750783368	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99916329	TCCTCCTAGGAGAAT[C/G]TCATCTTCTTACTTC	89122
rs750793753	snp	C/T			missense	TRIM4	GRCh38.p7	7:99903304	GAATAGTTCACATCC[C/T]GGATCTCACTCCTAA	89122
rs750814604	snp	A/C	1.65594e-05	0.0028774	stop-gained, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919020	TCACCCGGTAGCTCT[A/C]GAAGGCCTCGTCGAT	89122
rs750975177	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	TRIM4	GRCh38.p7	7:99892529	AACTTCCCAGTAATG[C/T]TTCCCTGAGGTGAAA	89122
rs751017679	snp	A/G	1.94676e-05	0.00311984	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919119	CCTCGCAGAAGAGCC[A/G]CAGCGGCTCCCAGTG	89122
rs751045462	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99903113	CCACCTTTCCTGACA[C/G]TCTATTAGCTGCATG	89122
rs751093780	snp	A/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890762	ATCAAAAAAGTATCT[A/T]TTGGGTACTATGCTT	89122
rs751200124	in-del	-/CCCTTCCC	1.93673e-05	0.00311179	intron-variant	TRIM4	GRCh38.p7	7:99892792	GCAGCTTATCATCAA[-/CCCTTCCC]CAGAAATGCCCATCT	89122
rs751265994	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912258	ACCATAGGCCAGGCA[C/T]GGTGGCTCACGCCTG	89122
rs751292429	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902260	TTTTAGTTTGTTTGT[C/T]TTTTGAGACAGAGTC	89122
rs751325934	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99916188	ACTTATATTTCCCTC[A/G]GCCCCCACCCACAAG	89122
rs751335448	in-del	-/C	3.30786e-05	0.00406672	intron-variant	TRIM4	GRCh38.p7	7:99916821	TTCCCTGCCTTAAAA[-/C]CCTTTTATAACTCCC	89122
rs751377646	snp	C/T	1.65373e-05	0.00287548	synonymous-codon	TRIM4	GRCh38.p7	7:99903249	CATTTCCTTCATCAA[C/T]GGTATCTGGCACACT	89122
rs751622753	snp	C/T	3.29598e-05	0.00405941	missense	TRIM4	GRCh38.p7	7:99892311	ACATTCCCAGTCCCA[C/T]GATCCAGGTAAACCC	89122
rs751643985	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99906096	GTTGCAGTGAGCCAA[G/T]ATCGCTCCACTGCAC	89122
rs751679112	snp	C/T	4.9543e-05	0.00497685	missense	TRIM4	GRCh38.p7	7:99908617	GAGCCTGGCTCTTCT[C/T]CCCCACCTCTAAGAT	89122
rs751710660	snp	A/G	3.36315e-05	0.00410057	missense	TRIM4	GRCh38.p7	7:99892206	ACTAAAGATGCTAAT[A/G]GACTCAACCAAAAAA	89122
rs751789824	snp	C/T			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919716	AGACCCAGAAATGCC[C/T]GTGGAAAGCTACAGA	89122
rs751831839	snp	A/T	3.30393e-05	0.0040643	intron-variant	TRIM4	GRCh38.p7	7:99916666	ATCCCTCCCTCTCCA[A/T]CATCCCTGCCCTGAA	89122
rs751859923	snp	C/G	0.000148776	0.00862357	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919289	CCCGGCGCCCAGTTG[C/G]GGTGCAGGCAGCCGC	89122
rs751951502	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915390	GGAAAAAAGAGCTGC[A/G]CTTGGAGGCCTTTTC	89122
rs751960914	snp	A/G/T	0.00066517	0.0182271	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919155	CGCACAGGCCCGGGG[A/G/T]CACGGGGCCCAGGCG	89122
rs752019648	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917612	TAATCCCAGCTACTC[A/G]GTAAGCTGAGGCAGG	89122
rs752112921	snp	G/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890785	CTATGCTTATTACCT[G/T]GGTAATGAAATAATA	89122
rs752126660	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896332	GCTCCTTTTCTAGGA[A/G]GGACATCTGAACATC	89122
rs752133575	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99895937	CTTTTCCAGTAAAAA[A/T]TTGGGTCTTATTTTT	89122
rs752156360	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915056	CTCAAGGGATCCTCG[C/T]GTCTCAGCCTCCCAA	89122
rs752170396	snp	A/G	1.83242e-05	0.00302684	intron-variant	TRIM4	GRCh38.p7	7:99909701	AGAAAACACATCTCC[A/G]ACCATCATCATCTTC	89122
rs752184466	snp	C/T	1.89651e-05	0.00307931	intron-variant	TRIM4	GRCh38.p7	7:99892782	AAGTAGTGCAGCAGC[C/T]TATCATCAACCCTTC	89122
rs752274217	snp	A/G	1.68185e-05	0.00289982	missense	TRIM4	GRCh38.p7	7:99892671	GAACTGGCTGATGCT[A/G]TATTTTTCACGTATC	89122
rs752364699	in-del	-/A	6.58903e-05	0.00573941	frameshift-variant	TRIM4	GRCh38.p7	7:99892483	CTCCCGACACACCCC[-/A]AACAGCAACCTCCAG	89122
rs752392295	snp	A/G	0.000113026	0.00751667	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919318	GCGGCAGAAGTTGTG[A/G]CCGCACTCGATGGAC	89122
rs752417758	snp	C/T	1.69542e-05	0.0029115	intron-variant	TRIM4	GRCh38.p7	7:99908847	GCTCACTCCTTTTTC[C/T]GCCTGACCCCAGCTA	89122
rs752621961	snp	A/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920831	TCTATGGAGAAGGGA[A/T]CTGGTTCTTTAATAG	89122
rs752751977	snp	G/T	7.32145e-05	0.00604995	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919345	GGACACCGGGTCCTG[G/T]AAATAGTCCAGGCAG	89122
rs752754182	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904718	CATGAAAAGTGCTCA[A/G]TCTCACTAGTTATCA	89122
rs752806534	snp	G/T	1.64762e-05	0.00287016	missense, intron-variant	TRIM4	GRCh38.p7	7:99916771	CACGTGGATGTCAAA[G/T]TTACCTGTCTAAAAC	89122
rs752919760	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897777	ACTGTCTTACTCTGG[C/T]CACTTGCAAAGCATT	89122
rs753001516	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	TRIM4	GRCh38.p7	7:99908636	CACCTCTAAGATGAG[C/T]TTCTTCAATGAAGCG	89122
rs753066490	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896194	AAGGTTTATGGTATC[A/G]TATGGCAGATGCACC	89122
rs753074823	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99907038	AAGGAAATCAATTTT[A/C]AAAATGGGTAGGTAG	89122
rs753091177	snp	C/T	7.56172e-05	0.00614841	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919409	GCTTCCATGCTGCTT[C/T]CCTGCCGCGGAGACG	89122
rs753173658	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911764	AACATACATTAATCC[C/T]AGGGTACAGCAATTC	89122
rs753207069	snp	C/T	6.59109e-05	0.0057403	missense	TRIM4	GRCh38.p7	7:99892332	AGGTAAACCCCCACT[C/T]GGTGGAGAGCTGGCT	89122
rs753315126	snp	C/T	7.241e-05	0.00601662	intron-variant	TRIM4	GRCh38.p7	7:99902141	TTGTTTCACATATTG[C/T]GCCTGTTTTGTTTTT	89122
rs753320916	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913802	CTTTTATAGAATGAA[A/G]ACATTTACTGACTTG	89122
rs753527282	snp	C/G/T	4.94233e-05	0.00497087	synonymous-codon, missense	TRIM4	GRCh38.p7	7:99908651	CTTCTTCAATGAAGC[C/G/T]ATAGTTTGATTGAGT	89122
rs753532034	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890429	GCATGTATATATTCA[C/T]TGCAGCACTATTCAC	89122
rs753581827	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99894977	CTGATCATTTTGATT[A/G]AAGGTGTGTCAATTT	89122
rs753626629	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99903053	CACCTTGTAACAGTG[C/T]GTTAAATAAATGTTT	89122
rs753651241	snp	A/G	1.80114e-05	0.00300089	intron-variant	TRIM4	GRCh38.p7	7:99902135	AAACGGTTGTTTCAC[A/G]TATTGTGCCTGTTTT	89122
rs753654930	snp	A/T	1.65507e-05	0.00287664	intron-variant	TRIM4	GRCh38.p7	7:99916652	CTCATTATCACTCCA[A/T]CCCTCCCTCTCCATC	89122
rs753835414	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99901093	AATAAGGCTGCATAA[A/T]GTTGTCCCACAGGTC	89122
rs753858337	snp	C/T	1.94517e-05	0.00311857	intron-variant	TRIM4	GRCh38.p7	7:99892794	AGCTTATCATCAACC[C/T]TTCCCCAGAAATGCC	89122
rs753982737	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99898398	CAATCCCTTCAAATA[C/G]CCAATAATATGTGGC	89122
rs754001362	snp	A/G	4.21594e-05	0.00459107	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919011	ACGGCCAGCTCACCC[A/G]GTAGCTCTCGAAGGC	89122
rs754050061	snp	A/G	1.69057e-05	0.00290733	intron-variant	TRIM4	GRCh38.p7	7:99903355	TTAGGGGACAACTAG[A/G]GTAGCCAAGACCTCC	89122
rs754078806	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897352	GGTGAAGCTGGGAAG[C/T]AAGTTCAAACAGAGT	89122
rs754099802	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99893968	ATCACATGGTTTTCC[-/T]TTTTTTTTTTTTTTT	89122
rs754155205	in-del	-/ATTT			intron-variant	TRIM4	GRCh38.p7	7:99895600	ACTATATCCCTGCTG[-/ATTT]ATTGCCTAATTATTC	89122
rs754210179	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893399	TAGAACCAAGGCTGC[C/T]GACTAGCTGGTTCTT	89122
rs754220704	snp	A/C/T	3.29545e-05	0.00405911	synonymous-codon, missense	TRIM4	GRCh38.p7	7:99892346	TCGGTGGAGAGCTGG[A/C/T]TCTTGCTGGGTGGGA	89122
rs754233219	snp	G/T	1.64741e-05	0.00286998	missense	TRIM4	GRCh38.p7	7:99908728	TGTTCAATCTCTGAA[G/T]AAACAGGTCCTCTTC	89122
rs754358547	snp	A/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917841	GGTGGGGCTACTCTG[A/G]AAAGGATGATCAGGG	89122
rs754467947	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99901251	CATCCAGTGCATTCT[A/T]CGCCTTAATCACATT	89122
rs754628346	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99901379	TGTGTCAATTCTAGG[A/T]CAGTTTCAGTTGATT	89122
rs754766924	in-del	-/CT			intron-variant	TRIM4	GRCh38.p7	7:99913195	TTCTACTACTCAAGA[-/CT]CTACCCAAGTTTTTT	89122
rs754886643	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920762	CCACTGAATATTTCT[A/G]AAACATTTAAATTGG	89122
rs754962071	in-del	-/AATTACATAT			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918693	ACCAGAAAGATTTTA[-/AATTACATAT]GTGGTTTCTATTGGA	89122
rs754985807	snp	A/C	1.64751e-05	0.00287007	synonymous-codon	TRIM4	GRCh38.p7	7:99908762	AACCAGGAAGTTGTG[A/C]AGCTTTGAAAACTCC	89122
rs755050023	in-del	-/TG			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920910	AGTGTTTATGGCATC[-/TG]TGTGTCTATATGTTT	89122
rs755115262	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99916476	CATTCCACAAGCATG[G/T]GATCTTCTGTCCTAA	89122
rs755129720	snp	A/G	6.58979e-05	0.00573974	synonymous-codon, intron-variant	TRIM4	GRCh38.p7	7:99916759	CTTCCATTCATCCAC[A/G]TGGATGTCAAAGTTA	89122
rs755217789	snp	C/G/T	0.000247774	0.0111281	intron-variant	TRIM4	GRCh38.p7	7:99916670	CTCCCTCTCCATCAT[C/G/T]CCTGCCCTGAACTAA	89122
rs755289921	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99894992	AAAGGTGTGTCAATT[C/T]TACTGAAATTCTCAA	89122
rs755367258	snp	A/G	1.648e-05	0.0028705	intron-variant	TRIM4	GRCh38.p7	7:99903554	GCCACCCAGGTCCCC[A/G]TAAGAGAACAGGAGT	89122
rs755394185	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99907741	GGTGGGTCCAGGTTT[C/T]TGACTTCCTTAAGAG	89122
rs755415544	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893440	CACACAGGTGTCACA[C/T]AGGACAGAATAATGA	89122
rs755434027	snp	A/G	0.000140361	0.0083762	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919297	CCAGTTGCGGTGCAG[A/G]CAGCCGCGGCAGAAG	89122
rs755474688	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99904634	GGTATGTGGGAACTC[C/T]GTCCCATCTTCTCAA	89122
rs755491586	snp	A/C			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917879	TCAAGCTAAAAGCTA[A/C]AAGGATCTAAAGGAT	89122
rs755501651	snp	C/G	1.66949e-05	0.00288915	missense	TRIM4	GRCh38.p7	7:99892215	GCTAATGGACTCAAC[C/G]AAAAAAATGGCCGGA	89122
rs755676392	in-del	-/C	6.74605e-05	0.00580738	frameshift-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919398	GGATGTCCTCAGCTT[-/C]CATGCTGCTTCCCTG	89122
rs755695366	snp	C/T	0.000186498	0.00965474	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919428	GCCGCGGAGACGGAG[C/T]CCGACGTGAGGCGCG	89122
rs755783128	snp	A/G	0.000109176	0.00738757	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919321	GCAGAAGTTGTGGCC[A/G]CACTCGATGGACACC	89122
rs755841618	snp	A/G	3.31603e-05	0.00407174	synonymous-codon	TRIM4	GRCh38.p7	7:99909631	CTTCATCTTGGCCAC[A/G]AGATTACGCTGAGAC	89122
rs755946853	snp	C/T			missense	TRIM4	GRCh38.p7	7:99892546	TCCCTGAGGTGAAAA[C/T]GTTTTTTCCCAGAAC	89122
rs755996620	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99914611	ACATCGCATGCCACC[-/T]TTCCCCTTGCTCTTG	89122
rs756003291	snp	A/G	1.72788e-05	0.00293923	intron-variant	TRIM4	GRCh38.p7	7:99908859	TTCTGCCTGACCCCA[A/G]CTACTAAATTCCTTA	89122
rs756059590	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99912586	GTTAATGATATACAT[A/G]CTGAAGTATTTTGTT	89122
rs756090052	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99898954	TTGTCTTTTGTTGCT[A/G]TAGTTTCTAACGCTG	89122
rs756193998	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99897152	GACCCCGTGAAGAGA[A/T]CTAGTGGCAGGGAGG	89122
rs756210577	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant	TRIM4	GRCh38.p7	7:99916773	CGTGGATGTCAAAGT[C/T]ACCTGTCTAAAACAA	89122
rs756312392	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918107	ACAAGCTAGGCTTTT[C/T]CCAAATCATCAGCTG	89122
rs756316095	snp	C/T	1.65296e-05	0.00287481	missense	TRIM4	GRCh38.p7	7:99903254	CCTTCATCAATGGTA[C/T]CTGGCACACTGTCTT	89122
rs756369331	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99907627	CATGTTGTAAAACTT[C/T]TACATAATTCTTGGA	89122
rs756402004	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891161	GTAACAAAATCAAAA[C/T]CTGAAACAAAGATCA	89122
rs756465619	snp	A/G	4.94352e-05	0.00497143	stop-gained	TRIM4	GRCh38.p7	7:99892333	GGTAAACCCCCACTC[A/G]GTGGAGAGCTGGCTC	89122
rs756527925	snp	A/G	1.6476e-05	0.00287014	synonymous-codon	TRIM4	GRCh38.p7	7:99908644	AGATGAGCTTCTTCA[A/G]TGAAGCGATAGTTTG	89122
rs756530604	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904307	ATCAAGAAAAAAACA[A/G]ACAAATTCCAATAGG	89122
rs756584084	snp	A/C	1.65135e-05	0.00287341	intron-variant	TRIM4	GRCh38.p7	7:99916676	CTCCATCATCCCTGC[A/C]CTGAACTAATTCAGG	89122
rs756622593	in-del	-/C	0.000214647	0.0103575	frameshift-variant	TRIM4	GRCh38.p7	7:99908616	GAGCCTGGCTCTTCT[-/C]CCCCCACCTCTAAGA	89122
rs756638722	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902542	ATGAGCCTTCGTGCC[C/T]GGCCTACAACATGGT	89122
rs756792761	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890852	AGAACAAACCTGCAC[A/G]TGTTCCCCTTAAACT	89122
rs756804064	in-del	-/TTTCTCT			intron-variant	TRIM4	GRCh38.p7	7:99915448	ATGAAGCTATTTCTC[-/TTTCTCT]TTTCTCTTTTCTCTT	89122
rs756832585	snp	A/C	5.05344e-05	0.00502639	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919440	GAGTCCGACGTGAGG[A/C]GCGGGAGAGGCCAGC	89122
rs756984489	snp	C/G	1.79615e-05	0.00299674	intron-variant	TRIM4	GRCh38.p7	7:99902081	TTTCACATTTCTCAG[C/G]AATCACCGTCCTTCA	89122
rs757008736	in-del	-/T	1.81519e-05	0.00301258	intron-variant	TRIM4	GRCh38.p7	7:99902145	TTCACATATTGTGCC[-/T]GTTTTGTTTTTGTGT	89122
rs757051663	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99898668	ACCTCGCTAAACATA[C/T]GGCTGCAGCCTTCAA	89122
rs757071882	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899635	CTGTCATGGATTTTA[C/T]TTTTAAATATAAGTT	89122
rs757082874	snp	C/T	7.04449e-05	0.00593443	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919349	ACCGGGTCCTGGAAA[C/T]AGTCCAGGCAGATGG	89122
rs757105115	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99910953	GGGTCCAGATTTAGC[C/T]CCTCAGTTGTGGTTT	89122
rs757111710	snp	C/T	1.65614e-05	0.00287757	intron-variant	TRIM4	GRCh38.p7	7:99916653	TCATTATCACTCCAT[C/T]CCTCCCTCTCCATCA	89122
rs757145672	snp	A/G	1.6951e-05	0.00291122	missense	TRIM4	GRCh38.p7	7:99892684	CTGTATTTTTCACGT[A/G]TCTCCCTTCCTGGGA	89122
rs757233379	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99909035	AACATTTCAGTCTCT[A/C]CTACTGACAAGTTTT	89122
rs757318936	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99907380	CTCCCAAAGTGTTGG[G/T]ATTACAGGCGTGAGC	89122
rs757337072	snp	C/T	1.64863e-05	0.00287104	missense	TRIM4	GRCh38.p7	7:99903284	TCACCTTTACAGCTT[C/T]AAGAGAATAGTTCAC	89122
rs757341685	snp	G/T	0.000169918	0.00921575	intron-variant	TRIM4	GRCh38.p7	7:99903356	TAGGGGACAACTAGG[G/T]TAGCCAAGACCTCCA	89122
rs757369892	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920494	GAAACCCAGCTGTTA[C/T]AAAAAATAAAGTAAG	89122
rs757450347	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906127	TCCAGCCTCGGCCAC[A/G]CAGCAAGACTCCATC	89122
rs757503450	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919719	CCCAGAAATGCCTGT[A/G]GAAAGCTACAGAGGA	89122
rs757588078	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99895947	AAAAAATTGGGTCTT[-/A]TTTTTTTTTTTTAGC	89122
rs757680360	snp	C/T	1.64732e-05	0.0028699	missense	TRIM4	GRCh38.p7	7:99892436	GCCCACATCTGGGGA[C/T]ATTTTTGAACGATCA	89122
rs757738094	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915394	AAAAGAGCTGCACTT[A/G]GAGGCCTTTTCCATG	89122
rs757770704	snp	C/G	1.65548e-05	0.002877	stop-gained, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919012	CGGCCAGCTCACCCG[C/G]TAGCTCTCGAAGGCC	89122
rs757778733	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890894	TAAAATAAAATCCTC[A/G]TTAAATCACTGCCTG	89122
rs757791044	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99914283	TAGTCTCGGCCTCCC[A/G]AATAGCTGGGACTAC	89122
rs757828171	snp	A/G	1.67337e-05	0.00289251	intron-variant	TRIM4	GRCh38.p7	7:99908826	TCCTAAGGCCACATG[A/G]GATTTGCTCACTCCT	89122
rs757860733	snp	A/G	4.9606e-05	0.00498002	intron-variant	TRIM4	GRCh38.p7	7:99916796	TAAAACAAAAAAAAC[A/G]ATCATATCATTCCCT	89122
rs757904380	snp	A/G	4.94189e-05	0.00497062	synonymous-codon	TRIM4	GRCh38.p7	7:99892448	GGACATTTTTGAACG[A/G]TCAGTAATTCCCATG	89122
rs757949169	snp	C/T	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892519	CTCTACTCTCAACTT[C/T]CCAGTAATGTTTCCC	89122
rs757977850	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902201	AAAACAACTCGTTTA[C/T]TTACTCCATTTTGGC	89122
rs757996629	snp	A/G	6.58979e-05	0.00573974	synonymous-codon	TRIM4	GRCh38.p7	7:99908753	CTCTTCTTCAACCAG[A/G]AAGTTGTGCAGCTTT	89122
rs758004077	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914138	TCTTTTGTCTGACAA[C/T]TACAATAACCTCCCG	89122
rs758082882	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99906807	GCTATGAGCACACCA[C/T]CGCACTCCAGTCTGG	89122
rs758210814	snp	C/T	3.29495e-05	0.00405877	synonymous-codon	TRIM4	GRCh38.p7	7:99908672	TTGATTGAGTTTTAA[C/T]GTGTTCTCATTCAGC	89122
rs758248623	snp	A/T	0.000267436	0.0115606	intron-variant	TRIM4	GRCh38.p7	7:99902167	TTTTTGTGTTTTTAT[A/T]TTAGTTGCTGCAGAC	89122
rs758257321	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99897379	GAGTGGGAGACAGTC[G/T]ATCCCACCCTCCCTG	89122
rs758310378	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99908822	CTTATCCTAAGGCCA[C/T]ATGAGATTTGCTCAC	89122
rs758313305	snp	A/T			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921525	CTCCCCTTCAAGACT[A/T]ACACAACCATGTCTC	89122
rs758443418	snp	G/T	0.000127089	0.00797047	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919447	ACGTGAGGCGCGGGA[G/T]AGGCCAGCAAGCTGC	89122
rs758516845	snp	C/T			upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919622	GCTGGGTATCCGCGC[C/T]GGAACCGCGAGGGGG	89122
rs758523386	snp	C/G	1.72943e-05	0.00294055	missense	TRIM4	GRCh38.p7	7:99892186	TATCAGTCACTGGTG[C/G]AATGACTAAAGATGC	89122
rs758729818	snp	A/G	4.24133e-05	0.00460487	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919021	CACCCGGTAGCTCTC[A/G]AAGGCCTCGTCGATG	89122
rs758831724	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911778	CTAGGGTACAGCAAT[C/T]CTACTCCTAGACCCT	89122
rs758909062	snp	A/C/T	4.94428e-05	0.00497186	intron-variant	TRIM4	GRCh38.p7	7:99903529	TCTGCTCAGCCTGTA[A/C/T]CTTTACCATGCCACC	89122
rs758923435	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914016	TATGAATTTCAGTCA[C/T]TGTAACTTCTGCAAT	89122
rs758969930	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99895947	AAAAATTGGGTCTTA[-/T]TTTTTTTTTTTTAGC	89122
rs758999657	snp	C/G	1.65446e-05	0.00287612	missense	TRIM4	GRCh38.p7	7:99903289	TTTACAGCTTCAAGA[C/G]AATAGTTCACATCCT	89122
rs759103702	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919750	CTTGGGCAAGGCGTT[A/G]GAGCCGGACGTTGTG	89122
rs759103780	snp	A/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890509	ATAAAGAAAACATAG[A/T]ACATATACACCATGG	89122
rs759189508	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99893078	ACATGGCGAAACCCC[A/G]TCTCTACTGAAAATA	89122
rs759211254	snp	G/T	1.79728e-05	0.00299768	splice-acceptor-variant	TRIM4	GRCh38.p7	7:99892748	TAGGTTTACAGCCAC[G/T]GTGGAGAAAATGAGA	89122
rs759292480	snp	A/C			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891633	TTCTATGCCTTTGTC[A/C]AATTTCACAAAAGTG	89122
rs759345449	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890522	AGTACATATACACCA[C/T]GGAATACTATGCAGC	89122
rs759351518	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99902912	CTGAATTTCTGTAAC[A/C]TTTTATTCCTACCAC	89122
rs759387451	snp	C/G	1.9971e-05	0.00315992	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919244	GGCGCCGATGGGTGC[C/G]GACATTCGGGGCAGG	89122
rs759406748	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902171	TGTGTTTTTATTTTA[A/G]TTGCTGCAGACAAGA	89122
rs759417256	in-del	-/TCAGGGGAAGAAAAGCC	1.87601e-05	0.00306263	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892146	GGGAAGGAGTTTTGG[-/TCAGGGGAAGAAAAGCC]TCATTTCCTATCAGT	89122
rs759462306	in-del	-/GC/GTGC			intron-variant	TRIM4	GRCh38.p7	7:99909157	TGTGTGTGTGTGTGT[-/GC/GTGC]GCGTGTGTGTGTGCA	89122
rs759515242	snp	A/G	1.92092e-05	0.00309907	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892133	CAGCTGGACTACAGG[A/G]AAGGAGTTTTGGTCA	89122
rs759544916	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99910024	GCCATGAGCCACCAC[A/G]CCTGGCAACTTCATT	89122
rs759653309	snp	C/G	1.64738e-05	0.00286995	missense	TRIM4	GRCh38.p7	7:99892423	AAATCGCCCAGATGC[C/G]CACATCTGGGGACAT	89122
rs759878981	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897601	AAAGATTTCTCAAGT[C/T]GGTTCTTGCACTCCA	89122
rs759934856	snp	C/T			synonymous-codon	TRIM4	GRCh38.p7	7:99909592	GGCGTTCTTCACTTC[C/T]ACATCCTGTAAATGC	89122
rs759944183	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920266	ACAGTTCATGAATTG[A/G]GCAGCACTCAGAACC	89122
rs759944808	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906816	ACACCACCGCACTCC[A/G]GTCTGGGTAACAAAG	89122
rs759968953	snp	C/G/T			intron-variant	TRIM4	GRCh38.p7	7:99899823	TTTGAGATGGGGTCT[C/G/T]GCTGTTGCCCATGCT	89122
rs759980325	snp	A/G	5.38721e-05	0.00518971	intron-variant	TRIM4	GRCh38.p7	7:99902120	CGTCTGGTGCTTTGA[A/G]AACGGTTGTTTCACA	89122
rs760093219	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99913848	AACAACATTAAACTT[C/G]CAAAGATCTTAGTTT	89122
rs760162721	snp	C/T	1.64765e-05	0.00287019	missense, intron-variant	TRIM4	GRCh38.p7	7:99916731	GGTACAAGAGCAGCC[C/T]AATTAGTCTTCTCTT	89122
rs760235661	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99895759	TTACATTCTCTTGAC[A/G]AACTGACCACTTTAT	89122
rs760304606	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99905723	GGGAGCAAAATCACC[C/T]TGATTCAAAACACTG	89122
rs760321781	snp	G/T	3.79817e-05	0.00435768	intron-variant	TRIM4	GRCh38.p7	7:99892783	AGTAGTGCAGCAGCT[G/T]ATCATCAACCCTTCC	89122
rs760331023	snp	A/G	5.15256e-05	0.00507544	intron-variant	TRIM4	GRCh38.p7	7:99903191	AAAGATTTCTAAGGA[A/G]CCCCAAGTCCTAGAA	89122
rs760379231	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901902	TCCGCTCCAGGATAC[C/T]GCCCAGTACTTTGCG	89122
rs760403674	snp	G/T	1.84783e-05	0.00303954	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892151	GGAGTTTTGGTCAGG[G/T]GAAGAAAAGCCTCAT	89122
rs760501339	in-del	-/TGTAT			intron-variant	TRIM4	GRCh38.p7	7:99910587	GTTTATCTATGTGTG[-/TGTAT]TGTATTTGTATGTGA	89122
rs760515312	snp	A/G	8.24531e-05	0.00642026	synonymous-codon	TRIM4	GRCh38.p7	7:99892274	GTGCAGGTGCACTCC[A/G]TCCACAGCGCTGTAG	89122
rs760560524	snp	A/G	1.71608e-05	0.00292918	intron-variant	TRIM4	GRCh38.p7	7:99908575	CCCCCACTCGTAACT[A/G]TCTCACCTGAAGCAG	89122
rs760619449	snp	A/C	1.86757e-05	0.00305573	intron-variant	TRIM4	GRCh38.p7	7:99909703	AAAACACATCTCCAA[A/C]CATCATCATCTTCTT	89122
rs760768618	snp	A/G	0.000102538	0.0071595	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919092	ACACCAGGCACACTG[A/G]CCGCTGGTCGTCCTC	89122
rs760786003	snp	A/G	1.65564e-05	0.00287714	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919002	GTCACCGCGACGGCC[A/G]GCTCACCCGGTAGCT	89122
rs760808584	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99898222	GAGCAGGTTAGTGCT[A/T]CCCCAGCTGTGGGGT	89122
rs760834782	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911751	CAGTGTAAAACTAAA[C/T]ATACATTAATCCTAG	89122
rs760883645	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99910283	TTTTGATGGACAACT[A/G]GCAGGATTTAACAAA	89122
rs760943805	snp	A/G			missense	TRIM4	GRCh38.p7	7:99892491	CACACCCCAACAGCA[A/G]CCTCCAGACTATCTC	89122
rs760981858	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917644	GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC	89122
rs760994998	snp	G/T	3.29468e-05	0.00405861	missense	TRIM4	GRCh38.p7	7:99908714	CTCTTCTTCTTCTTT[G/T]TTCAATCTCTGAAGA	89122
rs761085289	snp	A/C			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918808	GCACAATGATTGCTG[A/C]GGTTTGCACCTCCCC	89122
rs761132321	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99900675	CTTTAGTTTACCTCC[-/A]AACTTATTTATTTCA	89122
rs761136883	in-del	-/CC			intron-variant	TRIM4	GRCh38.p7	7:99894664	AGACCAAGACTCCAT[-/CC]CCCCCCCAAAAAAAA	89122
rs761177646	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99895258	GTATATTGTCTTTTC[C/T]TTTTCATTCCATTCA	89122
rs761245215	snp	C/T	6.81071e-05	0.00583515	intron-variant	TRIM4	GRCh38.p7	7:99903202	AGGAGCCCCAAGTCC[C/T]AGAAATTCTGCTCAC	89122
rs761348642	in-del	-/C			frameshift-variant	TRIM4	GRCh38.p7	7:99892563	TTTTTTCCCAGAACA[-/C]AGGGTAAGTGCTGAA	89122
rs761455176	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99904070	GAACTGAAAATACCC[G/T]AAGTTATAACACAAA	89122
rs761494839	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99916310	TTTTTTACTCTCTAT[A/G]TGGTCCTCCTAGGAG	89122
rs761498837	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913451	AGGCGGGCAGATTAC[A/G]AGGTCAGGAGTTCCA	89122
rs761501472	in-del	-/ACTG	4.56423e-05	0.00477693	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918969	ACTTTATCGGGCAAC[-/ACTG]ACAGCCCCGTCATAG	89122
rs761559474	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99913486	AGCCTGACCAACATG[C/G]TGAAACCCCGTCTTT	89122
rs761568983	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99916243	ATGGGTCCTCTCCAT[A/G]TCTTTTGCTGGCTAC	89122
rs761702045	snp	C/G	0.000231006	0.0107447	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918962	TAAGTAAACTTTATC[C/G]GGCAACACTGACAGC	89122
rs761718937	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912271	CACGGTGGCTCACGC[C/T]TGTAACCCCAGCATT	89122
rs761754125	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99894330	AGTTCTTGAAGAATT[A/G]GCATTTATTTCTTAA	89122
rs761770222	snp	C/T	1.82794e-05	0.00302314	intron-variant	TRIM4	GRCh38.p7	7:99902147	CACATATTGTGCCTG[C/T]TTTGTTTTTGTGTTT	89122
rs761967632	in-del	-/GAG			intron-variant	TRIM4	GRCh38.p7	7:99900766	TTTCAGGACTTTAAA[-/GAG]TTTGCTTACTGGCAT	89122
rs762053152	snp	A/C	1.84487e-05	0.0030371	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919110	GCTGGTCGTCCTCGC[A/C]GAAGAGCCGCAGCGG	89122
rs762090265	snp	G/T	1.64874e-05	0.00287113	intron-variant	TRIM4	GRCh38.p7	7:99903611	ATTCTGTGAAAAGAA[G/T]GAAGACATAAGCAAA	89122
rs762156933	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99909857	CCCACCTCAGCCTCC[A/C]AAGTAGCTGGACTAC	89122
rs762238470	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99896988	GCAACTAGGGAGATA[C/T]TAGCTCAGGCTAATT	89122
rs762258884	snp	C/T	1.64974e-05	0.00287201	missense	TRIM4	GRCh38.p7	7:99892588	GCTGAAATCTCTCTA[C/T]AAAAGCAGTCTTCTG	89122
rs762296876	snp	A/G	1.66765e-05	0.00288756	intron-variant	TRIM4	GRCh38.p7	7:99908821	TCTTATCCTAAGGCC[A/G]CATGAGATTTGCTCA	89122
rs762346990	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99905090	GAAAGGTGTACATAC[-/AT]ATATATATATATATC	89122
rs762420655	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916140	GCTGAAGATGGAAGA[C/T]TTAAGGGCTATGTTC	89122
rs762420815	snp	C/T			missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919053	GTGCCATGGCGTGAG[C/T]CTGGTGCTCCTGGGA	89122
rs762447808	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99909272	GAGGGGTGCTACCTT[-/A]AAGTAGAGACATGGG	89122
rs762555501	in-del	-/ATTA			intron-variant	TRIM4	GRCh38.p7	7:99898781	GGGTGGAAGCTGCAC[-/ATTA]ATTAAAACCAAATGT	89122
rs762624048	snp	C/T	1.65908e-05	0.00288012	missense	TRIM4	GRCh38.p7	7:99909579	CCTTCCACTGTGTGG[C/T]GTTCTTCACTTCTAC	89122
rs762773538	snp	C/T	6.04723e-05	0.00549841	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919072	GTGCTCCTGGGACTC[C/T]CTGCACACCAGGCAC	89122
rs762791443	snp	A/G	4.53628e-05	0.00476228	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918972	TTATCGGGCAACACT[A/G]ACAGCCCCGTCATAG	89122
rs762807748	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99913091	TTTCACTTTGCTTGA[C/T]AATGAAAAATATAAT	89122
rs762817835	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891681	GGGATGTTCACACTA[C/T]GTCCCTTTAGTGCAG	89122
rs762827898	snp	C/T	3.36293e-05	0.00410043	intron-variant	TRIM4	GRCh38.p7	7:99903340	TAGAGAAGACTGCTC[C/T]TAGGGGACAACTAGG	89122
rs762845805	in-del	-/C	0.00442861	0.0468475	intron-variant	TRIM4	GRCh38.p7	7:99916794	CTAAAACAAAAAAAA[-/C]CGATCATATCATTCC	89122
rs762890554	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99903931	AGCAGCTCCAGCTTT[C/G]AGCTTCCACTCTTCT	89122
rs762931584	in-del	-/ATTA			intron-variant	TRIM4	GRCh38.p7	7:99917421	CATTTTCACTGTGTC[-/ATTA]AATTCATGTGTTTGG	89122
rs763018220	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900451	CTGTGGCCCAGTCAA[A/G]TTGATGTATAAACTT	89122
rs763095395	snp	C/G	1.65425e-05	0.00287593	missense	TRIM4	GRCh38.p7	7:99908610	AGGGTGGGAGCCTGG[C/G]TCTTCTCCCCCACCT	89122
rs763102423	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99911382	AAATTACAAAACTAG[-/T]TGAATAGTGTCAAAT	89122
rs763155379	snp	C/G/T	0.000128653	0.00801953	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919389	ACTCCTCCTGGATGT[C/G/T]CTCAGCTTCCATGCT	89122
rs763220193	snp	G/T	5.31166e-05	0.0051532	missense	TRIM4	GRCh38.p7	7:99892735	CTGTGTCTTCAGCTA[G/T]GTTTACAGCCACTGT	89122
rs763306675	snp	C/G	0.000174749	0.00934579	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919275	GGAACGGGCCGCCGC[C/G]CGGCGCCCAGTTGCG	89122
rs763327068	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921494	TCAAGTATAAAACTG[A/G]AGGGATGCTTCAGTT	89122
rs763351309	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902373	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	89122
rs763355087	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99908291	TAATTATAAATGTAC[A/C]CATAAGATGAATGAA	89122
rs763387987	snp	A/G	1.65649e-05	0.00287788	missense	TRIM4	GRCh38.p7	7:99892615	TCTGAGGATTCCTCC[A/G]TCCAGCAAAGTAGTT	89122
rs763438855	in-del	-/AAAT			intron-variant	TRIM4	GRCh38.p7	7:99913674	GACTCCATCTCAAAT[-/AAAT]AAATAAATAAATAAA	89122
rs763591408	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917286	AATGTTTGGCAAATA[A/G]TAAGCATCAATAAAC	89122
rs763718940	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99903081	TTTCTTGAATGAAGT[C/G]TATACCCATTTATTA	89122
rs763750154	snp	C/G	9.98851e-05	0.0070663	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919430	CGCGGAGACGGAGTC[C/G]GACGTGAGGCGCGGG	89122
rs763801344	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99910937	TGGCTGCAGGAGGAA[A/G]GGGTCCAGATTTAGC	89122
rs763809208	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916180	ACCCATCCACTTATA[C/T]TTCCCTCGGCCCCCA	89122
rs763852214	in-del	-/G	1.64747e-05	0.00287003	frameshift-variant	TRIM4	GRCh38.p7	7:99892547	CCCTGAGGTGAAAAC[-/G]TTTTTTCCCAGAACA	89122
rs763861941	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915371	TCCTAGAGTCAGGCA[C/T]GAAGGAAAAAAGAGC	89122
rs763916647	in-del	-/C	0.00442861	0.0468475	intron-variant	TRIM4	GRCh38.p7	7:99916795	CTAAAACAAAAAAAA[-/C]GATCATATCATTCCC	89122
rs763935971	snp	C/T	1.94256e-05	0.00311647	intron-variant	TRIM4	GRCh38.p7	7:99892793	CAGCTTATCATCAAC[C/T]CTTCCCCAGAAATGC	89122
rs763952363	snp	C/T	6.1512e-05	0.00554547	intron-variant	TRIM4	GRCh38.p7	7:99909712	CTCCAACCATCATCA[C/T]CTTCTTTTTTCTTTT	89122
rs764031797	snp	C/T	4.21701e-05	0.00459165	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919010	GACGGCCAGCTCACC[C/T]GGTAGCTCTCGAAGG	89122
rs764088266	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, intron-variant	TRIM4	GRCh38.p7	7:99916737	AGAGCAGCCTAATTA[A/G]TCTTCTCTTCCATTC	89122
rs764096369	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891701	CTTTAGTGCAGTTAC[A/G]GTACTTCAGGCTGCA	89122
rs764222632	snp	C/T	1.65277e-05	0.00287464	missense	TRIM4	GRCh38.p7	7:99903256	TTCATCAATGGTATC[C/T]GGCACACTGTCTTCA	89122
rs764342795	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900473	TATAAACTTACCATC[A/G]CAATTCCTTTTTAAA	89122
rs764361139	snp	A/G	1.69143e-05	0.00290807	intron-variant	TRIM4	GRCh38.p7	7:99903353	TCTTAGGGGACAACT[A/G]GGGTAGCCAAGACCT	89122
rs764379499	snp	A/G	0.000106958	0.00731214	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919095	CCAGGCACACTGGCC[A/G]CTGGTCGTCCTCGCA	89122
rs764394942	snp	C/T	1.64735e-05	0.00286993	missense	TRIM4	GRCh38.p7	7:99908715	TCTTCTTCTTCTTTG[C/T]TCAATCTCTGAAGAA	89122
rs764499225	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99896931	AGCCCCCAAGGTTGA[C/G]CTTGTGGCACAGGCA	89122
rs764552117	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99908377	ATCAACTTATCTCCT[A/G]TGAGCTGAGCTCAGC	89122
rs764562450	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99896279	GTGGGTTCACACTTC[C/T]AAGCTAAGAAATGTG	89122
rs764574437	snp	A/G	3.29451e-05	0.00405851	missense	TRIM4	GRCh38.p7	7:99892474	CCATGACGTCCTCCC[A/G]ACACACCCCAACAGC	89122
rs764590844	snp	C/T	1.65798e-05	0.00287917	missense	TRIM4	GRCh38.p7	7:99908808	CGCTGACTCTTTATC[C/T]TATCCTAAGGCCACA	89122
rs764592930	snp	G/T	1.64738e-05	0.00286995	synonymous-codon	TRIM4	GRCh38.p7	7:99892433	GATGCCCACATCTGG[G/T]GACATTTTTGAACGA	89122
rs764750145	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99915054	ACCTCAAGGGATCCT[C/G]GCGTCTCAGCCTCCC	89122
rs764763229	snp	C/G			upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919925	AGGCCAGGAAGACTT[C/G]AAGGATCTGTGTTGG	89122
rs764796513	snp	G/T	6.68509e-05	0.00578114	intron-variant	TRIM4	GRCh38.p7	7:99908824	TATCCTAAGGCCACA[G/T]GAGATTTGCTCACTC	89122
rs764848920	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893207	AGAAGGCGGAGGTTG[C/T]AGTGACCCGAGATCG	89122
rs764872137	snp	C/T	0.000133485	0.00816851	missense	TRIM4	GRCh38.p7	7:99903226	TGCTCACCTTGGAAT[C/T]GCTTTAGCATTTCCT	89122
rs764956366	snp	C/T	3.29489e-05	0.00405874	synonymous-codon	TRIM4	GRCh38.p7	7:99908738	CTGAAGAAACAGGTC[C/T]TCTTCTTCAACCAGG	89122
rs765054352	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99910492	GACATGAAATACACA[A/G]TAAGTTGAAAGCAAG	89122
rs765091297	snp	C/T	1.84978e-05	0.00304114	intron-variant	TRIM4	GRCh38.p7	7:99902152	ATTGTGCCTGTTTTG[C/T]TTTTGTGTTTTTATT	89122
rs765102071	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99906530	TTTATTATGACAATA[A/T]ATATAACAATTTGTC	89122
rs765132809	snp	A/G	4.94181e-05	0.00497057	synonymous-codon	TRIM4	GRCh38.p7	7:99892466	AGTAATTCCCATGAC[A/G]TCCTCCCGACACACC	89122
rs765139914	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902944	AGCAAACACTGGCTC[C/T]TACTATATCACTGTG	89122
rs765166518	snp	A/G	4.59274e-05	0.00479182	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918963	AAGTAAACTTTATCG[A/G]GCAACACTGACAGCC	89122
rs765168431	in-del	-/T	1.64827e-05	0.00287073	frameshift-variant	TRIM4	GRCh38.p7	7:99892299	CTGTAGAAGGAGACA[-/T]TCCCAGTCCCACGAT	89122
rs765210148	snp	C/T	1.68335e-05	0.00290111	intron-variant	TRIM4	GRCh38.p7	7:99903215	CCTAGAAATTCTGCT[C/T]ACCTTGGAATCGCTT	89122
rs765360048	snp	A/C	0.000188947	0.0097179	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919268	GGGCAGGGGAACGGG[A/C]CGCCGCCCGGCGCCC	89122
rs765362192	snp	C/T	1.69642e-05	0.00291236	intron-variant	TRIM4	GRCh38.p7	7:99903361	GACAACTAGGGTAGC[C/T]AAGACCTCCACTCCC	89122
rs765508336	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99897611	CAAGTCGGTTCTTGC[A/T]CTCCATGGGGGAAAG	89122
rs765527347	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99912121	AGAATAACTGGGAAA[A/G]GGCATGAAAGAATTC	89122
rs765536179	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899331	TAAATGAAAATGCTA[C/T]ATATAACCTGCATGC	89122
rs765565036	snp	G/T	1.64871e-05	0.00287111	intron-variant	TRIM4	GRCh38.p7	7:99903612	TTCTGTGAAAAGAAG[G/T]AAGACATAAGCAAAT	89122
rs765639206	snp	A/C	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892493	CACCCCAACAGCAAC[A/C]TCCAGACTATCTCTA	89122
rs765746400	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905920	GAAGCCAAGGCAGGC[A/G]GATCACTCGAGGTCA	89122
rs765759563	snp	A/G			missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919226	TTGGGTCGCAGCGCG[A/G]CGGGCGCCGATGGGT	89122
rs765765867	snp	C/G/T	3.31045e-05	0.00406834	missense	TRIM4	GRCh38.p7	7:99892608	GCAGTCTTCTGAGGA[C/G/T]TCCTCCATCCAGCAA	89122
rs765915735	snp	A/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99889918	GACAGCATAACTCCA[A/G]TCCAATCTCTGCCTC	89122
rs765932327	snp	C/T	1.66172e-05	0.00288242	missense	TRIM4	GRCh38.p7	7:99892626	CTCCATCCAGCAAAG[C/T]AGTTCCATGCTGAAG	89122
rs765941379	snp	C/T	1.68525e-05	0.00290275	intron-variant	TRIM4	GRCh38.p7	7:99908837	CATGAGATTTGCTCA[C/T]TCCTTTTTCTGCCTG	89122
rs765981544	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905739	TGATTCAAAACACTG[A/G]TGTACAGCAATGAAA	89122
rs766007111	snp	C/T	3.29495e-05	0.00405877	missense, intron-variant	TRIM4	GRCh38.p7	7:99916754	CTTCTCTTCCATTCA[C/T]CCACGTGGATGTCAA	89122
rs766061909	snp	C/T	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892524	CTCTCAACTTCCCAG[C/T]AATGTTTCCCTGAGG	89122
rs766103827	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99894727	CGAAAGCCATTTGGA[A/G]GGTTTCTAATAGCAA	89122
rs766165161	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99893386	GTTGAATCAAAACTA[G/T]AACCAAGGCTGCCGA	89122
rs766210337	snp	A/G	1.65501e-05	0.00287659	missense	TRIM4	GRCh38.p7	7:99903244	TTTAGCATTTCCTTC[A/G]TCAATGGTATCTGGC	89122
rs766431344	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99898338	TAATAGCATGTCACA[A/G]GCTAAACTCTTAATG	89122
rs766484231	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99906010	ATTAGCCAGGTGTGG[A/T]GGCACACGCCTGTAA	89122
rs766560455	snp	C/T	1.65414e-05	0.00287583	intron-variant	TRIM4	GRCh38.p7	7:99916659	TCACTCCATCCCTCC[C/T]TCTCCATCATCCCTG	89122
rs766566332	snp	C/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920477	CTCGGCCGTGATTGG[C/G]TGAAACCCAGCTGTT	89122
rs766591771	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918832	CCTCCCCTCCTCTCA[C/T]TCCAGTTTTAACCCT	89122
rs766615194	snp	C/T	1.6884e-05	0.00290547	synonymous-codon	TRIM4	GRCh38.p7	7:99892202	AATGACTAAAGATGC[C/T]AATGGACTCAACCAA	89122
rs766659328	in-del	-/TTAG			intron-variant	TRIM4	GRCh38.p7	7:99902247	ACAACATGGTTCTTT[-/TTAG]TTTGTTTGTTTTTTG	89122
rs766737818	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	TRIM4	GRCh38.p7	7:99892295	AGCGCTGTAGAAGGA[A/G]ACATTCCCAGTCCCA	89122
rs766806455	snp	A/C	0.000733682	0.019139	missense	TRIM4	GRCh38.p7	7:99892740	TCTTCAGCTAGGTTT[A/C]CAGCCACTGTGGAGA	89122
rs766870187	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99897289	AGACTTGCCTCCACC[G/T]GAAAGAAGGCAGACC	89122
rs766917046	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99899249	GTCCATTCCTTGGAA[A/T]GCAGGCAATACAGGG	89122
rs767050420	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99913526	ACAAAAAAAAATTAG[C/T]CGGGCATGGTGGCAC	89122
rs767182091	snp	A/T	1.67618e-05	0.00289493	missense	TRIM4	GRCh38.p7	7:99892660	ACACTGGCCAAGAAC[A/T]GGCTGATGCTGTATT	89122
rs767245728	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904152	TGTTCCTTAAGCCAT[A/G]AAATGAAACAGTAGA	89122
rs767284207	in-del	-/G	9.86242e-05	0.00702156	frameshift-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919048	GATGGGTGCCATGGC[-/G]TGAGTCTGGTGCTCC	89122
rs767306914	snp	C/T	1.85806e-05	0.00304794	intron-variant	TRIM4	GRCh38.p7	7:99892770	AAAATGAGAGCTAAG[C/T]AGTGCAGCAGCTTAT	89122
rs767434735	snp	A/C/T	0.000260455	0.0114088	intron-variant	TRIM4	GRCh38.p7	7:99908568	GAGATCACCCCCACT[A/C/T]GTAACTGTCTCACCT	89122
rs767530595	snp	C/T	4.94205e-05	0.0049707	missense	TRIM4	GRCh38.p7	7:99892426	TCGCCCAGATGCCCA[C/T]ATCTGGGGACATTTT	89122
rs767643308	snp	C/T	9.88484e-05	0.00702954	missense, intron-variant	TRIM4	GRCh38.p7	7:99916764	ATTCATCCACGTGGA[C/T]GTCAAAGTTACCTGT	89122
rs767722088	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902745	GATACCCACCCCTCC[A/G]TGTTCTCCACACCTT	89122
rs767749747	in-del	-/CTGACA			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921314	TCCTTGCTAGAGGAG[-/CTGACA]CTTTTTGCCACAGGA	89122
rs767817520	snp	A/T	6.64209e-05	0.00576247	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919396	CTGGATGTCCTCAGC[A/T]TCCATGCTGCTTCCC	89122
rs767855511	snp	A/G			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917754	TAAATAAATAAATTC[A/G]TGTGTTCATGTACTT	89122
rs767897065	snp	C/T	4.94205e-05	0.0049707	missense	TRIM4	GRCh38.p7	7:99908707	TCTTCGTCTCTTCTT[C/T]TTCTTTGTTCAATCT	89122
rs767938033	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99897014	TAATTTCTGTCCCAC[C/T]TGTGGGAACAGGATG	89122
rs768053980	snp	C/G	1.64789e-05	0.0028704	synonymous-codon	TRIM4	GRCh38.p7	7:99892316	CCCAGTCCCACGATC[C/G]AGGTAAACCCCCACT	89122
rs768068498	snp	A/G	3.29641e-05	0.00405968	synonymous-codon	TRIM4	GRCh38.p7	7:99908629	TCTCCCCCACCTCTA[A/G]GATGAGCTTCTTCAA	89122
rs768103636	snp	A/G	4.96676e-05	0.00498311	intron-variant	TRIM4	GRCh38.p7	7:99916828	CCTTAAAACCCTTTT[A/G]TAACTCCCCACTGCC	89122
rs768178462	in-del	-/C	1.6473e-05	0.00286988	frameshift-variant	TRIM4	GRCh38.p7	7:99892509	TCCAGACTATCTCTA[-/C]TCTCAACTTCCCAGT	89122
rs768224292	snp	C/G	1.71082e-05	0.00292469	intron-variant	TRIM4	GRCh38.p7	7:99903195	ATTTCTAAGGAGCCC[C/G]AAGTCCTAGAAATTC	89122
rs768246973	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99899013	ACATACCTTGCCTCA[C/G]GGAAGTTGCAGAGAA	89122
rs768297424	snp	A/G	1.65979e-05	0.00288074	synonymous-codon	TRIM4	GRCh38.p7	7:99903300	AAGAGAATAGTTCAC[A/G]TCCTGGATCTCACTC	89122
rs768298237	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99911332	TGAAAAACCAAGAGA[C/G]AATGGTTTCTCCTAT	89122
rs768307282	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99899202	CAACCCAGAAATGCA[A/C]TCCTCATCTATAAAG	89122
rs768389447	snp	A/T	5.29479e-05	0.00514501	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919058	ATGGCGTGAGTCTGG[A/T]GCTCCTGGGACTCCC	89122
rs768402827	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919571	CAAAAAGAACGCACG[G/T]ACGTTGCCCGGCCTG	89122
rs768410130	snp	C/T	1.64727e-05	0.00286986	missense	TRIM4	GRCh38.p7	7:99892456	TTGAACGATCAGTAA[C/T]TCCCATGACGTCCTC	89122
rs768441027	in-del	-/ATT			intron-variant	TRIM4	GRCh38.p7	7:99897500	TACCCTGATTTTATC[-/ATT]ATGCACTGTATACAT	89122
rs768564777	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99894187	GAATTTAGGTATCTA[C/T]GTTCATGAGAGACAT	89122
rs768663046	snp	A/C	1.64754e-05	0.00287009	missense	TRIM4	GRCh38.p7	7:99892392	ATCAAGGGCCAATAG[A/C]CAGCAGCACTCCAAT	89122
rs768664529	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914488	AAAACTAATCAGATA[C/T]TGTCACTCTCCTGCT	89122
rs768719601	snp	A/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891515	AGAGAGAGTGCAACA[A/T]AGGCAGAGTGAGGGG	89122
rs768737130	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901677	ACGCTACTCAGTGCC[C/T]GTGAACTACGAGTTT	89122
rs768766939	snp	A/G	1.64822e-05	0.00287068	synonymous-codon	TRIM4	GRCh38.p7	7:99892571	CAGAACACAGGGTAA[A/G]TGCTGAAATCTCTCT	89122
rs768768697	snp	G/T	1.67108e-05	0.00289052	missense	TRIM4	GRCh38.p7	7:99909654	GCTGAGACTTAAGAA[G/T]TTTCTCCTGCCAGCA	89122
rs768790581	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99914542	CTTCACCAAGAAAAT[A/C]TGAACACTTCATTGT	89122
rs768840515	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915723	GATATCAGGGAATTC[C/T]GCCCAGTGACCTGGC	89122
rs768997182	snp	C/G	0.000204019	0.0100979	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919261	ACATTCGGGGCAGGG[C/G]AACGGGCCGCCGCCC	89122
rs769047308	in-del	-/CTT	1.64738e-05	0.00286995	cds-indel	TRIM4	GRCh38.p7	7:99908687	CGTGTTCTCATTCAG[-/CTT]CTTCTTCGTCTCTTC	89122
rs769067170	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99909461	GCATCCAAGACTCTA[C/T]GTGAACTGCAAAACC	89122
rs769109476	in-del	-/C	9.88533e-05	0.00702971	frameshift-variant, intron-variant	TRIM4	GRCh38.p7	7:99916768	TCCACGTGGATGTCA[-/C]AAGTTACCTGTCTAA	89122
rs769138861	snp	C/T	1.72597e-05	0.00293761	intron-variant	TRIM4	GRCh38.p7	7:99909542	CTCAGGAGCAAGAAA[C/T]ATCCAACCACTTCTG	89122
rs769225250	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921502	AAAACTGGAGGGATG[C/G]TTCAGTTCTCCCCTT	89122
rs769227818	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99897824	ACTTTGTATTATAAA[A/C]CAGGCGCCAGGCCAC	89122
rs769329171	snp	C/T	2.70691e-05	0.00367883	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919191	GCTGCGTCTTCTCAG[C/T]CAGCCTGGCCAGGGC	89122
rs769355334	in-del	-/TA			intron-variant	TRIM4	GRCh38.p7	7:99898006	CAGAACACAACAGAC[-/TA]TTGGGTCTGCAGAGA	89122
rs769372024	in-del	-/CA			intron-variant	TRIM4	GRCh38.p7	7:99893367	ATATTAACAAATTCT[-/CA]CACGTTGAATCAAAA	89122
rs769390069	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99909282	ACCTTAAAGTAGAGA[C/T]ATGGGGATGAAGTAT	89122
rs769443292	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99908034	AAAGGAGGGGCTTTT[A/G]ATAACAAACTGGCCT	89122
rs769457795	snp	A/G	1.64792e-05	0.00287042	intron-variant	TRIM4	GRCh38.p7	7:99903570	TAAGAGAACAGGAGT[A/G]CATACCTGGTCAACA	89122
rs769528584	in-del	-/AAAGA			intron-variant	TRIM4	GRCh38.p7	7:99894695	AAAAGAAAAGAAAAG[-/AAAGA]AAAGAAACAAAACGA	89122
rs769560760	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905534	ACAGTACTATACAGC[A/G]GGCACTACTGACATT	89122
rs769615191	in-del	-/AT			intron-variant	TRIM4	GRCh38.p7	7:99905092	AAGGTGTACATACAT[-/AT]ATATATATATATCCA	89122
rs769621409	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99896702	TCAGGGGAGAATCCA[C/T]GGTGGAAATCCTGGG	89122
rs769655366	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916082	AAATGCTTAGAACTG[C/T]GGGTGGTACGTAAGA	89122
rs769749528	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99917103	ATTTAACTCCTCAAC[A/G]GAGCCTTTCCTCACT	89122
rs769766371	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915554	TTAAAACACAGTCCA[C/T]CCATCTGAGTATATG	89122
rs769827119	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99912839	TACAGTTCTGTTAAA[A/T]GGCACAATACCATCT	89122
rs769972381	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99914484	TCTAAAAACTAATCA[C/G]ATATTGTCACTCTCC	89122
rs769980710	snp	C/T	1.79438e-05	0.00299526	intron-variant	TRIM4	GRCh38.p7	7:99902092	TCAGGAATCACCGTC[C/T]TTCACTGCCTGACGT	89122
rs770128143	snp	C/G	1.6674e-05	0.00288734	synonymous-codon	TRIM4	GRCh38.p7	7:99908597	CTGAAGCAGCTCCAG[C/G]GTGGGAGCCTGGCTC	89122
rs770148766	snp	A/C	6.11154e-05	0.00552756	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919374	AGATGGGGCAGGTCA[A/C]CTCCTCCTGGATGTC	89122
rs770230620	snp	C/T	1.7528e-05	0.00296036	missense	TRIM4	GRCh38.p7	7:99892726	TGGGATGAGCTGTGT[C/T]TTCAGCTAGGTTTAC	89122
rs770241327	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99902240	AACACCCACAACATG[C/G]TTCTTTTTAGTTTGT	89122
rs770246153	snp	G/T	1.66101e-05	0.0028818	synonymous-codon	TRIM4	GRCh38.p7	7:99909574	CATTACCTTCCACTG[G/T]GTGGCGTTCTTCACT	89122
rs770306624	in-del	-/TTC			intron-variant	TRIM4	GRCh38.p7	7:99896082	TTTGTCCTATATGTT[-/TTC]TTCTTTTTCTGCCTT	89122
rs770324244	snp	A/C			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890935	CTGAAAATCTGGGAG[A/C]AAATATATTGAAATG	89122
rs770361294	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99917325	GTGAAGGAATGAACA[-/T]ACACTTTCTAGTCCA	89122
rs770402442	snp	A/C	1.65091e-05	0.00287303	synonymous-codon	TRIM4	GRCh38.p7	7:99892250	TGAGACAGAAGAACA[A/C]GAAAAGGTGTGCAGG	89122
rs770413244	in-del	-/CATA			intron-variant	TRIM4	GRCh38.p7	7:99900931	TTTCTTCATATTTCT[-/CATA]CTCAGGGTTTGTTGA	89122
rs770417579	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99907892	GGTTCTGAGGCATCC[A/G]ATACTCAACATGAAT	89122
rs770428475	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901547	ATGCAGTTAAGTTAG[C/T]TGGAAAGAGTTTGAC	89122
rs770468534	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921155	TTCATTCAGAGAAGT[A/G]GAATCACTATGTTTC	89122
rs770492472	snp	C/T	1.75228e-05	0.00295991	intron-variant	TRIM4	GRCh38.p7	7:99908561	TGAAGATGAGATCAC[C/T]CCCACTCGTAACTGT	89122
rs770492567	snp	C/T	1.96077e-05	0.00313104	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892113	GCCCAGGGATGTGTG[C/T]CCCTCAGCTGGACTA	89122
rs770597775	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99906756	GAGATCAAGGCAGGA[A/C]AATTACTTGAGCCCA	89122
rs770636070	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99894390	TCATCTGGGGACCAG[G/T]CGCGGTGGCTCATGC	89122
rs770672061	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919693	GTGGCTCCTCCAAAC[A/G]GCTATAGAGACCCAG	89122
rs770677061	snp	C/T	6.24746e-05	0.00558869	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919074	GCTCCTGGGACTCCC[C/T]GCACACCAGGCACAC	89122
rs770690383	snp	C/T	1.7312e-05	0.00294205	intron-variant	TRIM4	GRCh38.p7	7:99909680	CAGCAGAAACACACA[C/T]AGGTAAGAAAACACA	89122
rs770772754	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99916032	AGAATCCACCTAATA[G/T]GATGTCTATGAAGAT	89122
rs770931167	snp	C/G	0.00035823	0.0133786	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919229	GGTCGCAGCGCGGCG[C/G]GCGCCGATGGGTGCC	89122
rs770997658	snp	A/C	3.2975e-05	0.00406035	missense	TRIM4	GRCh38.p7	7:99908781	TTTGAAAACTCCGTG[A/C]TGATTCTCATTCGCT	89122
rs771031368	in-del	-/T			intron-variant	TRIM4	GRCh38.p7	7:99906361	CCACGAGTGTCATAC[-/T]TTTTTTTTTTAAATA	89122
rs771053588	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99909448	CAGAGGTTCTGAGGC[A/T]TCCAAGACTCTACGT	89122
rs771064839	in-del	-/A	0	0	intron-variant	TRIM4	GRCh38.p7	7:99916786	TTACCTGTCTAAAAC[-/A]AAAAAAAACGATCAT	89122
rs771212971	snp	A/C/T	3.29464e-05	0.00405861	synonymous-codon	TRIM4	GRCh38.p7	7:99908696	ATTCAGCTTCTTCTT[A/C/T]GTCTCTTCTTCTTCT	89122
rs771219735	snp	A/G	1.64743e-05	0.00287	missense	TRIM4	GRCh38.p7	7:99892413	GCACTCCAATAAATC[A/G]CCCAGATGCCCACAT	89122
rs771296121	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900191	CCAGATAGAGCCAGC[A/G]TTCTAGTTGGAAGGC	89122
rs771359754	snp	A/G	5.38121e-05	0.00518683	intron-variant	TRIM4	GRCh38.p7	7:99902106	CCTTCACTGCCTGAC[A/G]TCTGGTGCTTTGAAA	89122
rs771399181	snp	C/T	2.11732e-05	0.00325364	intron-variant	TRIM4	GRCh38.p7	7:99902197	CAAGAAAACAACTCG[C/T]TTATTTACTCCATTT	89122
rs771461090	snp	A/G/T	3.29817e-05	0.00406078	intron-variant	TRIM4	GRCh38.p7	7:99916691	CCTGAACTAATTCAG[A/G/T]TCTTTATTACCTCCT	89122
rs771539380	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920036	AAGTAGCAACCATTT[C/T]GCTATCCCAAAGAAC	89122
rs771551934	snp	C/T	1.6477e-05	0.00287024	missense	TRIM4	GRCh38.p7	7:99892375	GAGTTCCAGGGAAGC[C/T]TATCAAGGGCCAATA	89122
rs771569348	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913259	AGGTGAGTTAACTTG[A/G]CAGCCTTGGTGGAAG	89122
rs771720064	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918702	ATTTTAAATTACATA[C/T]GTGGTTTCTATTGGA	89122
rs771763287	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99905660	TAACCACCCTCCAGT[A/T]GTGACAACCAAAAAT	89122
rs771773085	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99899903	TTAAGCCATCCTCCC[A/G]CCGTGGCCTCCCAAG	89122
rs771774530	in-del	-/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890709	GAACAACAGACACCA[-/G]GGACTACTTGAGGGT	89122
rs771789934	snp	C/T	5.39011e-05	0.00519111	intron-variant	TRIM4	GRCh38.p7	7:99902123	CTGGTGCTTTGAAAA[C/T]GGTTGTTTCACATAT	89122
rs771818194	in-del	-/TCT			intron-variant	TRIM4	GRCh38.p7	7:99916333	CCTAGGAGAATCTCA[-/TCT]TCTTACTTCTTCCAT	89122
rs771881648	snp	C/T	1.64833e-05	0.00287078	splice-donor-variant, intron-variant	TRIM4	GRCh38.p7	7:99916701	TTCAGGTCTTTATTA[C/T]CTCCTGCTTAAAATG	89122
rs772037279	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896604	GACACAGTGCCATCC[A/G]TACTGAAATCAATAG	89122
rs772082253	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99895587	ATTATTCAAGTCTAC[C/T]ATATCCCTGCTGATT	89122
rs772130314	snp	A/G	1.64779e-05	0.00287031	missense	TRIM4	GRCh38.p7	7:99892564	TTTTTCCCAGAACAC[A/G]GGGTAAGTGCTGAAA	89122
rs772216262	snp	A/G	0.000160284	0.00895076	intron-variant	TRIM4	GRCh38.p7	7:99909524	GTCCCAGACCAAAAG[A/G]ACCTCAGGAGCAAGA	89122
rs772301253	in-del	-/TCT	2.23097e-05	0.00333982	intron-variant	TRIM4	GRCh38.p7	7:99909712	CTCCAACCATCATCA[-/TCT]TCTTTTTTCTTTTTG	89122
rs772359447	snp	C/T	1.6473e-05	0.00286988	missense	TRIM4	GRCh38.p7	7:99892467	GTAATTCCCATGACG[C/T]CCTCCCGACACACCC	89122
rs772360594	in-del	-/G			downstream-variant-500B	TRIM4	GRCh38.p7	7:99890191	CAGCAAATATCCTGG[-/G]AAGTTGAGAACTCAG	89122
rs772382452	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99899069	TTCAAGGGTATGCTG[G/T]ACTGCAGTGTACGGC	89122
rs772608109	snp	C/G	8.84271e-05	0.00664874	intron-variant	TRIM4	GRCh38.p7	7:99902207	ACTCGTTTATTTACT[C/G]CATTTTGGCTAGAAG	89122
rs772661593	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99909884	CTACAGGCATGCTCC[A/G]TCAGGTCCAACTAAT	89122
rs772790425	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920081	TCAACAAATAATATG[C/T]TCACCTGTTTCAGGG	89122
rs772812340	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99894446	CAAGGCAGTGGATTA[C/T]GAGGTCAGGAGTTCA	89122
rs772930862	snp	G/T	4.61478e-05	0.00480331	intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918964	AGTAAACTTTATCGG[G/T]CAACACTGACAGCCC	89122
rs772937366	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914554	AATCTGAACACTTCA[C/T]TGTGGCCCAACATAA	89122
rs773110031	snp	G/T	6.32931e-05	0.00562517	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919384	GGTCAACTCCTCCTG[G/T]ATGTCCTCAGCTTCC	89122
rs773110679	snp	A/C	1.67576e-05	0.00289457	intron-variant	TRIM4	GRCh38.p7	7:99903328	CTCCTAAGAAGGTAG[A/C]GAAGACTGCTCTTAG	89122
rs773114128	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99909913	ATTTTTTTATGTTTC[A/G]TAGAGACAAAGTCTC	89122
rs773198656	snp	C/G	0.000114896	0.00757859	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919067	GTCTGGTGCTCCTGG[C/G]ACTCCCTGCACACCA	89122
rs773308938	in-del	-/G	7.65492e-05	0.00618617	utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892136	CTGGACTACAGGGAA[-/G]GAGTTTTGGTCAGGG	89122
rs773376523	snp	A/G	0.000185443	0.00962741	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919270	GCAGGGGAACGGGCC[A/G]CCGCCCGGCGCCCAG	89122
rs773415980	snp	C/T	0.000115307	0.00759211	missense	TRIM4	GRCh38.p7	7:99892446	GGGGACATTTTTGAA[C/T]GATCAGTAATTCCCA	89122
rs773556525	snp	A/G	3.39974e-05	0.00412281	intron-variant	TRIM4	GRCh38.p7	7:99909669	GTTTCTCCTGCCAGC[A/G]GAAACACACACAGGT	89122
rs773637171	snp	A/G	3.30918e-05	0.00406753	synonymous-codon	TRIM4	GRCh38.p7	7:99908609	CAGGGTGGGAGCCTG[A/G]CTCTTCTCCCCCACC	89122
rs773760737	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99899082	TGGACTGCAGTGTAC[A/G]GCAGACACACCTGAC	89122
rs773812051	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99911746	AGGTTCAGTGTAAAA[C/T]TAAACATACATTAAT	89122
rs773814499	snp	A/G	1.65091e-05	0.00287303	missense	TRIM4	GRCh38.p7	7:99892252	AGACAGAAGAACAAG[A/G]AAAGGTGTGCAGGTG	89122
rs773826216	snp	A/G	5.2849e-05	0.0051402	synonymous-codon	TRIM4	GRCh38.p7	7:99892730	ATGAGCTGTGTCTTC[A/G]GCTAGGTTTACAGCC	89122
rs773850068	snp	C/T	1.78245e-05	0.00298529	missense	TRIM4	GRCh38.p7	7:99892741	CTTCAGCTAGGTTTA[C/T]AGCCACTGTGGAGAA	89122
rs773862812	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99903990	TAAATTATAATCGCA[A/T]GGGATATTTTATCAT	89122
rs773948464	snp	A/C	4.34141e-05	0.00465888	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919234	CAGCGCGGCGGGCGC[A/C]GATGGGTGCCGACAT	89122
rs774000696	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99917206	AATTAATGTTGTACA[C/T]GCTTAAGTTCCTTAC	89122
rs774037696	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899032	AGTTGCAGAGAATGA[C/T]GTGATAAGAATGTGG	89122
rs774056397	in-del	-/TAGA			intron-variant	TRIM4	GRCh38.p7	7:99907051	TTAAAAATGGGTAGG[-/TAGA]TAGATAAGTACAGTA	89122
rs774171729	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916235	TTTATCTGATGGGTC[C/T]TCTCCATGTCTTTTG	89122
rs774210115	snp	G/T	1.648e-05	0.0028705	missense	TRIM4	GRCh38.p7	7:99903579	AGGAGTGCATACCTG[G/T]TCAACACTTCTTTTG	89122
rs774210818	snp	A/G	1.75742e-05	0.00296425	intron-variant	TRIM4	GRCh38.p7	7:99909687	AACACACACAGGTAA[A/G]AAAACACATCTCCAA	89122
rs774217720	snp	C/T	0.000192252	0.00980251	synonymous-codon, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919090	GCACACCAGGCACAC[C/T]GGCCGCTGGTCGTCC	89122
rs774387063	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99892819	AATGCCCATCTTTTC[C/T]AGCATCAGTTTCATC	89122
rs774468985	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99905557	CTGACATTTTGGGCT[A/G]GATAAGTCTTTGCTG	89122
rs774621750	in-del	-/TCT	6.58957e-05	0.00573964	cds-indel	TRIM4	GRCh38.p7	7:99908700	AGCTTCTTCTTCGTC[-/TCT]TCTTCTTCTTTGTTC	89122
rs774631581	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99902499	TGATCCGCCTGCCTC[A/G]ACCTCCCAAAGTGCT	89122
rs774655730	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99898080	TGCTGCTAACTTGAG[C/T]ACCTGGAGCCATGTC	89122
rs774679769	snp	C/T	3.29451e-05	0.00405851	missense	TRIM4	GRCh38.p7	7:99892465	CAGTAATTCCCATGA[C/T]GTCCTCCCGACACAC	89122
rs774733858	snp	C/G	1.7938e-05	0.00299478	intron-variant	TRIM4	GRCh38.p7	7:99902108	TTCACTGCCTGACGT[C/G]TGGTGCTTTGAAAAC	89122
rs774771548	snp	C/T	1.64738e-05	0.00286995	missense	TRIM4	GRCh38.p7	7:99892422	TAAATCGCCCAGATG[C/T]CCACATCTGGGGACA	89122
rs774787376	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99908384	TATCTCCTATGAGCT[A/G]AGCTCAGCATACCTA	89122
rs774791061	snp	C/T	0.000266427	0.0115387	stop-gained	TRIM4	GRCh38.p7	7:99909568	TTCTGCCATTACCTT[C/T]CACTGTGTGGCGTTC	89122
rs775007844	snp	C/G	1.64806e-05	0.00287054	missense, intron-variant	TRIM4	GRCh38.p7	7:99916707	TCTTTATTACCTCCT[C/G]CTTAAAATGGTACAA	89122
rs775071800	snp	C/T	1.65296e-05	0.00287481	intron-variant	TRIM4	GRCh38.p7	7:99916816	TATCATTCCCTGCCT[C/T]AAAACCCTTTTATAA	89122
rs775162479	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99909288	AAGTAGAGACATGGG[A/G]ATGAAGTATGCGGAA	89122
rs775182653	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99894744	GTTTCTAATAGCAAT[G/T]TCTTTCATAGAAATA	89122
rs775199072	snp	C/G			missense	TRIM4	GRCh38.p7	7:99892610	AGTCTTCTGAGGATT[C/G]CTCCATCCAGCAAAG	89122
rs775263357	snp	G/T	1.72886e-05	0.00294007	intron-variant	TRIM4	GRCh38.p7	7:99903179	TTCTCCTATTTGAAA[G/T]ATTTCTAAGGAGCCC	89122
rs775276542	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99903864	CTGCCGGCCTCCCCA[A/G]CTAGTCTCAATCACA	89122
rs775331530	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99917134	CCTCAGTGATCACTC[C/G]GACCTCAGACCTTCT	89122
rs775388976	snp	A/C/G	3.29458e-05	0.00405857	missense	TRIM4	GRCh38.p7	7:99892473	CCCATGACGTCCTCC[A/C/G]GACACACCCCAACAG	89122
rs775448654	snp	C/G	0.00018712	0.00967083	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919365	AGTCCAGGCAGATGG[C/G]GCAGGTCAACTCCTC	89122
rs775484485	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99916787	TTACCTGTCTAAAAC[-/A]AAAAAAACGATCATA	89122
rs775491130	in-del	-/TT			upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919923	GAAGGCCAGGAAGAC[-/TT]GAAGGATCTGTGTTG	89122
rs775671416	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99901598	TGATTTGTAAGGTGG[G/T]TGTGGAGCAGCACCC	89122
rs775724802	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99900405	CCTCAAAAAAACACC[C/G]AAAATAATTTTTGAC	89122
rs775778525	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99900106	ATAAGATTTAATATA[A/G]GGAACTGGCTTGTGT	89122
rs775842125	snp	A/G	8.23934e-05	0.00641794	synonymous-codon	TRIM4	GRCh38.p7	7:99892565	TTTTCCCAGAACACA[A/G]GGTAAGTGCTGAAAT	89122
rs775846360	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99913410	GCGGTGGCTCACGCC[C/T]GTAATCCCAGCACTT	89122
rs775847990	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921447	CAAAGTAGATGAGCC[A/G]CAGTAGCACCTAGTG	89122
rs775952000	snp	C/G	1.65359e-05	0.00287536	missense	TRIM4	GRCh38.p7	7:99908799	ATTCTCATTCGCTGA[C/G]TCTTTATCTTATCCT	89122
rs776042163	snp	C/T	1.64735e-05	0.00286993	missense	TRIM4	GRCh38.p7	7:99908712	GTCTCTTCTTCTTCT[C/T]TGTTCAATCTCTGAA	89122
rs776140734	snp	C/T	1.7047e-05	0.00291945	intron-variant	TRIM4	GRCh38.p7	7:99903201	AAGGAGCCCCAAGTC[C/T]TAGAAATTCTGCTCA	89122
rs776145999	snp	C/T	1.65567e-05	0.00287716	intron-variant	TRIM4	GRCh38.p7	7:99916829	CTTAAAACCCTTTTA[C/T]AACTCCCCACTGCCT	89122
rs776238214	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99916956	CCATGCTCCATGCTC[C/G]AGAAGTACTGAGCAA	89122
rs776334740	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99907993	GACACTTTACCTACA[C/G]AGGATATAAAGGTAA	89122
rs776426468	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916061	ATTAAAGAATTACAG[C/T]ATGAAAAATGCTTAG	89122
rs776473848	snp	C/T	1.6476e-05	0.00287014	stop-gained, intron-variant	TRIM4	GRCh38.p7	7:99916747	AATTAGTCTTCTCTT[C/T]CATTCATCCACGTGG	89122
rs776527653	snp	A/T	3.29478e-05	0.00405867	synonymous-codon	TRIM4	GRCh38.p7	7:99892409	AGCAGCACTCCAATA[A/T]ATCGCCCAGATGCCC	89122
rs776613877	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99914746	AGCAAGTTTCAGCTG[C/T]AATGTCACCTCCTAA	89122
rs776633231	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99906031	ACGCCTGTAATCCCA[G/T]CTACTTGGGAGGCTG	89122
rs776812909	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99913327	GGAGGTGGCAGGAGC[A/G]CAACACCAAGCATTT	89122
rs776861402	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99893818	ATGTGTTAATAATGT[C/G]CTCCCTGGCCTCCCT	89122
rs776923095	snp	A/C	4.98409e-05	0.00499179	splice-acceptor-variant	TRIM4	GRCh38.p7	7:99908813	ACTCTTTATCTTATC[A/C]TAAGGCCACATGAGA	89122
rs776933096	snp	C/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99920257	GCACAAAGAACAGTT[C/G]ATGAATTGGGCAGCA	89122
rs777022852	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99897423	TCCCACTTAGTAGAA[A/G]TGGATTTTGAATGTT	89122
rs777100871	snp	C/T	1.64906e-05	0.00287142	missense	TRIM4	GRCh38.p7	7:99892582	GTAAGTGCTGAAATC[C/T]CTCTACAAAAGCAGT	89122
rs777192846	snp	C/G	1.66994e-05	0.00288953	splice-donor-variant	TRIM4	GRCh38.p7	7:99909564	CCACTTCTGCCATTA[C/G]CTTCCACTGTGTGGC	89122
rs777205420	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890703	AAAAGGGAACAACAG[A/G]CACCAGGGACTACTT	89122
rs777206883	snp	G/T			intron-variant	TRIM4	GRCh38.p7	7:99902156	TGCCTGTTTTGTTTT[G/T]GTGTTTTTATTTTAG	89122
rs777225196	snp	C/G	1.64792e-05	0.00287042	splice-donor-variant	TRIM4	GRCh38.p7	7:99903575	GAACAGGAGTGCATA[C/G]CTGGTCAACACTTCT	89122
rs777466585	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921558	TTGGGCTATTCTAAC[C/G]AGAAACAAAAGGAAA	89122
rs777556590	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99893928	CTAGAGTTTGACAAA[C/T]GCTTTTCCTGCTTCC	89122
rs777573423	snp	C/T	3.3211e-05	0.00407485	missense	TRIM4	GRCh38.p7	7:99909638	TTGGCCACGAGATTA[C/T]GCTGAGACTTAAGAA	89122
rs777659820	snp	A/G	1.64749e-05	0.00287005	synonymous-codon	TRIM4	GRCh38.p7	7:99892547	CCCTGAGGTGAAAAC[A/G]TTTTTTCCCAGAACA	89122
rs777662129	snp	A/G	7.53703e-05	0.00613836	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919205	GTCAGCCTGGCCAGG[A/G]CCCAGTTGGGTCGCA	89122
rs777855742	snp	C/T	2.02251e-05	0.00317996	intron-variant	TRIM4	GRCh38.p7	7:99902182	TTTAGTTGCTGCAGA[C/T]AAGAAAACAACTCGT	89122
rs777906535	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918171	CCAATACAGTATCCA[C/T]TTAGCCATACAAGCA	89122
rs777909197	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99907790	CTTGCTTATGAAAAA[A/G]AAATAGTAATGGTAG	89122
rs777969263	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904800	ACTTTGGGAGGCTTA[A/G]GTGGGTGGATCACTT	89122
rs778045965	snp	C/G	1.64776e-05	0.00287028	missense	TRIM4	GRCh38.p7	7:99892342	CCACTCGGTGGAGAG[C/G]TGGCTCTTGCTGGGT	89122
rs778111419	snp	C/T	3.58725e-05	0.00423497	intron-variant	TRIM4	GRCh38.p7	7:99902093	CAGGAATCACCGTCC[C/T]TCACTGCCTGACGTC	89122
rs778194773	in-del	-/TTTT			intron-variant	TRIM4	GRCh38.p7	7:99899807	GTTTTCTGGGTTTTC[-/TTTT]GAGATGGGGTCTCGC	89122
rs778197411	snp	A/C	1.65116e-05	0.00287324	intron-variant	TRIM4	GRCh38.p7	7:99916677	TCCATCATCCCTGCC[A/C]TGAACTAATTCAGGT	89122
rs778308208	snp	A/T	3.29576e-05	0.00405928	splice-acceptor-variant, intron-variant	TRIM4	GRCh38.p7	7:99916781	TCAAAGTTACCTGTC[A/T]AAAACAAAAAAAACG	89122
rs778310599	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99914103	AACCCCACTGCCACC[A/G]CTAGTTGAAGCCACC	89122
rs778319787	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99899426	AGGTCTTCAATAAAC[C/T]CCATGTCTCATTCAC	89122
rs778340045	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99901252	ATCCAGTGCATTCTT[C/T]GCCTTAATCACATTT	89122
rs778528058	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99899850	TGCTGGAGTGCAGTG[A/G]TGCAATCACAGCTCA	89122
rs778552498	snp	A/G	1.64773e-05	0.00287026	missense	TRIM4	GRCh38.p7	7:99892359	GGCTCTTGCTGGGTG[A/G]GAGTTCCAGGGAAGC	89122
rs778608451	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99901537	TTATCCTGGGATGCA[C/G]TTAAGTTAGTTGGAA	89122
rs778674105	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99912685	GACAGCTATGTGATA[A/G]AAGAGTCAAATGTTA	89122
rs778779026	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99907671	AATTTTAACTGTTAG[C/G]TTATATCTATCATAT	89122
rs778812204	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918714	ATATGTGGTTTCTAT[C/T]GGACAGCAGCGGCAC	89122
rs778890595	snp	A/C/G	8.72252e-05	0.00660351	intron-variant	TRIM4	GRCh38.p7	7:99908564	AGATGAGATCACCCC[A/C/G]ACTCGTAACTGTCTC	89122
rs778900133	snp	A/C			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99917897	GGATCTAAAGGATAG[A/C]TGTGGGTAGAGAAAG	89122
rs778966370	snp	A/G	6.99962e-05	0.0059155	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919350	CCGGGTCCTGGAAAT[A/G]GTCCAGGCAGATGGG	89122
rs778971772	snp	A/G	1.78957e-05	0.00299124	intron-variant	TRIM4	GRCh38.p7	7:99909519	GAAATGTCCCAGACC[A/G]AAAGGACCTCAGGAG	89122
rs778977189	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99906455	TCTCAGTTTCCCAAA[C/G]TGCTGGAATTACAGA	89122
rs778988669	snp	C/T			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921114	CTCCATCACAAAATG[C/T]CTATAAGTCTGTATA	89122
rs779034190	snp	C/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919893	GTTCTGGGCGAGCTG[C/T]AGCCTAGGGGCCTGG	89122
rs779056387	in-del	-/A			intron-variant	TRIM4	GRCh38.p7	7:99894673	CTCCATCCCCCCCCC[-/A]AAAAAAAAAAGAAAA	89122
rs779092005	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916611	ACCCACCAAGTCTAA[C/T]TGATCACCAAGTCAT	89122
rs779102867	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99911360	TATGCCAAAGGAAGA[A/G]ACCATTTAAATTACA	89122
rs779143691	snp	A/T			intron-variant	TRIM4	GRCh38.p7	7:99915739	GCCCAGTGACCTGGC[A/T]CCTGAACACCTACGA	89122
rs779252807	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99893524	ACAGATCATTCAAAA[C/G]TGAACTAATTATCTT	89122
rs779269024	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99911728	TACCACCATTTTGGA[A/C]GAAGGTTCAGTGTAA	89122
rs779362890	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99898966	GCTGTAGTTTCTAAC[A/G]CTGCTGCAGCATCTG	89122
rs779366105	in-del	-/TA			intron-variant	TRIM4	GRCh38.p7	7:99907989	TAAGGACACTTTACC[-/TA]CAGAGGATATAAAGG	89122
rs779385274	snp	A/T	8.23621e-05	0.00641672	missense	TRIM4	GRCh38.p7	7:99892449	GACATTTTTGAACGA[A/T]CAGTAATTCCCATGA	89122
rs779472200	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99912587	TTAATGATATACATG[C/T]TGAAGTATTTTGTTT	89122
rs779483842	in-del	-/T	7.31288e-05	0.00604641	utr-variant-5-prime, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919404	CCTCAGCTTCCATGC[-/T]GCTTCCCTGCCGCGG	89122
rs779534019	snp	A/G	1.64876e-05	0.00287116	missense	TRIM4	GRCh38.p7	7:99903287	CCTTTACAGCTTCAA[A/G]AGAATAGTTCACATC	89122
rs779574778	snp	G/T	0.000106093	0.00728253	intron-variant	TRIM4	GRCh38.p7	7:99902198	AAGAAAACAACTCGT[G/T]TATTTACTCCATTTT	89122
rs779670752	snp	G/T			upstream-variant-2KB, nc-transcript-variant	TRIM4, LOC101927610	GRCh38.p7	7:99919726	ATGCCTGTGGAAAGC[G/T]ACAGAGGACTTGGGC	89122
rs779735420	snp	G/T	1.65614e-05	0.00287757	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919025	CGGTAGCTCTCGAAG[G/T]CCTCGTCGATGGGTG	89122
rs779833401	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99904966	GAACCTGGGGGGCGA[A/G]GTTGCAGTAAGCCAA	89122
rs779933063	in-del	-/GC			intron-variant	TRIM4	GRCh38.p7	7:99898982	CTGCTGCAGCATCTG[-/GC]AGCAATGCTACTGCA	89122
rs779987744	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99899784	CACGTGCATGCATGC[A/C]CCTGTGAGTTTTCTG	89122
rs780017157	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99900992	TATTATATTCAGAAA[A/C]TCTTTGGCCATTATG	89122
rs780029838	snp	C/T			intron-variant, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99918324	TTAATCCCAGCACTA[C/T]GGGAGGCCAAGCGGG	89122
rs780043118	snp	A/C	1.77735e-05	0.00298101	intron-variant	TRIM4	GRCh38.p7	7:99909527	CCAGACCAAAAGGAC[A/C]TCAGGAGCAAGAAAT	89122
rs780141349	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915643	TAACTAACTTGGGGT[A/G]GGGATGGAATGAAAG	89122
rs780158226	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99896551	CCTCAATAAATCCTA[C/T]GTCTCATTCACCGGC	89122
rs780288162	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99897325	AATGCAGGATTATAC[A/C]GCTGTGGAAATGGTG	89122
rs780394514	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99893528	ATCATTCAAAACTGA[A/C]CTAATTATCTTACTT	89122
rs780418450	snp	A/G	3.36927e-05	0.00410429	intron-variant	TRIM4	GRCh38.p7	7:99903346	AGACTGCTCTTAGGG[A/G]ACAACTAGGGTAGCC	89122
rs780471594	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99916439	CCTTGGACTTCCTGT[C/G]ACAATTACTTCACAC	89122
rs780511981	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99892029	CACAAAGGGCAGATA[C/T]CAAACGGTACCGTTA	89122
rs780530479	snp	A/G	1.65477e-05	0.00287638	missense	TRIM4	GRCh38.p7	7:99903290	TTACAGCTTCAAGAG[A/G]ATAGTTCACATCCTG	89122
rs780607265	in-del	-/TTGA	1.64749e-05	0.00287005	frameshift-variant	TRIM4	GRCh38.p7	7:99908657	CAATGAAGCGATAGT[-/TTGA]TTGAGTTTTAACGTG	89122
rs780616029	snp	A/C	1.66565e-05	0.00288583	missense, upstream-variant-2KB	TRIM4, LOC101927610	GRCh38.p7	7:99919060	GGCGTGAGTCTGGTG[A/C]TCCTGGGACTCCCTG	89122
rs780647349	in-del	-/TGTT			intron-variant	TRIM4	GRCh38.p7	7:99902248	AACATGGTTCTTTTT[-/TGTT]AGTTTGTTTGTTTTT	89122
rs780678449	snp	C/T			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99891908	TGTCTTCCCCGCACA[C/T]CTCTTTAAAAGCTAC	89122
rs780704246	snp	A/G			utr-variant-3-prime	TRIM4	GRCh38.p7	7:99890954	TATATTGAAATGTTA[A/G]TAGTGCATAACTTTA	89122
rs780802219	in-del	-/TTTA	2.11649e-05	0.003253	intron-variant	TRIM4	GRCh38.p7	7:99902197	CAAGAAAACAACTCG[-/TTTA]TTTACTCCATTTTGG	89122
rs780863209	snp	A/G			upstream-variant-2KB, intron-variant	TRIM4, LOC101927610	GRCh38.p7	7:99921161	CAGAGAAGTGGAATC[A/G]CTATGTTTCTTTATG	89122
rs780878344	in-del	-/ACA			intron-variant	TRIM4	GRCh38.p7	7:99896629	CAATAGGGGTCTAGC[-/ACA]ACAATTAGCCCAGCA	89122
rs781090856	snp	A/T	6.5925e-05	0.00574092	missense	TRIM4	GRCh38.p7	7:99908775	TGCAGCTTTGAAAAC[A/T]CCGTGCTGATTCTCA	89122
rs781098041	in-del	-/G			intron-variant	TRIM4	GRCh38.p7	7:99902963	TATATCACTGTGAGT[-/G]CTGTGTGTCTGTCTC	89122
rs781153083	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99898717	ATTACTCTTCTCACT[A/G]GGCAACTGTGTAAAA	89122
rs781257141	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99915048	CTCCTGACCTCAAGG[A/G]ATCCTCGCGTCTCAG	89122
rs781270811	snp	A/G	1.64732e-05	0.0028699	missense	TRIM4	GRCh38.p7	7:99892536	CAGTAATGTTTCCCT[A/G]AGGTGAAAACGTTTT	89122
rs781285227	snp	G/T	1.69075e-05	0.00290748	intron-variant	TRIM4	GRCh38.p7	7:99908842	GATTTGCTCACTCCT[G/T]TTTCTGCCTGACCCC	89122
rs781290710	snp	A/C	1.64727e-05	0.00286986	missense	TRIM4	GRCh38.p7	7:99892460	ACGATCAGTAATTCC[A/C]ATGACGTCCTCCCGA	89122
rs781316910	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99906218	GAGGAGAAGGGAAGA[A/G]GTACTGATTGGGGAC	89122
rs781361828	snp	A/C	1.64969e-05	0.00287196	intron-variant	TRIM4	GRCh38.p7	7:99903634	TAAGCAAATTACGAA[A/C]CTTCTCCTGGAGACC	89122
rs781389852	snp	C/G			intron-variant	TRIM4	GRCh38.p7	7:99895252	ATTCTGGTATATTGT[C/G]TTTTCCTTTTCATTC	89122
rs781552287	snp	C/T	1.66109e-05	0.00288187	synonymous-codon	TRIM4	GRCh38.p7	7:99892223	ACTCAACCAAAAAAA[C/T]GGCCGGAGGCGTGAG	89122
rs781634877	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99902498	ATGATCCGCCTGCCT[C/T]GACCTCCCAAAGTGC	89122
rs781651283	snp	C/T	1.67761e-05	0.00289617	synonymous-codon	TRIM4	GRCh38.p7	7:99909658	AGACTTAAGAAGTTT[C/T]TCCTGCCAGCAGAAA	89122
rs781760722	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99915408	TGGAGGCCTTTTCCA[C/T]GCAAACAATTTGCAT	89122
rs781763461	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99901499	GCTCTTTTTTTGTTT[A/C]TTTCTACCAATTTTC	89122
rs796201795	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99896496	TAGCAACTGGTTTTC[A/G]TGTCCAGCCCACTGC	89122
rs796604480	snp	A/C			intron-variant	TRIM4	GRCh38.p7	7:99909773	AGTCTCACTTTGTCA[A/C]CCAGGTTAGACTGCA	89122
rs796833423	in-del	-/TGC			intron-variant	TRIM4	GRCh38.p7	7:99908256	TGGGAGTTTTATGCT[-/TGC]TTTGTTTTATTGTTT	89122
rs796923104	snp	C/T			intron-variant	TRIM4	GRCh38.p7	7:99916226	TCCCTTCCATTTATC[C/T]GATGGGTCCTCTCCA	89122
rs796959237	snp	A/G			intron-variant	TRIM4	GRCh38.p7	7:99899991	GGGTCTCACTATGTT[A/G]CCCAGGCTGGCCTCA	89122
rs796983837	in-del	-/AA			intron-variant	TRIM4	GRCh38.p7	7:99894673	CTCCATCCCCCCCCC[-/AA]AAAAAAAAAGAAAAG	89122

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