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

TOLLIP

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs527327416	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281019	CCACTCTGCAGCTCC[A/G]TGGAAGAGAACATGC	54472
rs527341485	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297329	CACTTCAAAGGACCC[C/T]GAGAGGGTCTAGCTC	54472
rs527433983	in-del	-/TGAT	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291127	CCGTGGCAAGTAAGA[-/TGAT]TGATTGTTCAGCAAA	54472
rs527575690	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1283731	CAATGTTATCTGTCA[C/T]CTGAATGCTCTTTCA	54472
rs527724006	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287082	GATAAGTCACTGCAC[C/T]GCTGCCGTCTCTGAG	54472
rs527725597	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288798	GAGACAAGAGGGAGA[A/G]GCCCCAGGCATCAGG	54472
rs527762138	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292847	ACCAGCTAGGAGGAC[C/T]GGGTATGCGGGCTGC	54472
rs527767561	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275837	ATTCTCTTTCTGTCC[A/G]TTATCAGTGGGTTTA	54472
rs527806118	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298415	GTCACAGGGACGTGT[A/G]GGCGTGGGGTCCAGA	54472
rs527839476	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303356	AGGGACGGCATGTGA[C/T]GTGGCAGGCCCTGGG	54472
rs527978970	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308576	TCATCTCTGAGTCAG[G/T]CTACACCAGCTCTCC	54472
rs528015510	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308053	TGAAAAAGGACTTTT[C/T]CCACCCACGGCATGT	54472
rs528066905	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279030	GGCAACATGAGGAAC[C/G]GAGGCACCGTGCTCC	54472
rs528119342	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278742	TGCTCATCAGCCTTT[C/T]GGCAATGACGGAAAA	54472
rs528141153	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1288230	CTGTGGGGAGGAGCC[C/T]GGTGTCCTGCAGGGC	54472
rs528158121	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283330	AGGGAGGCAAGGCCA[C/T]GGAGGGCCAGTGACC	54472
rs528311908	snp	A/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1291858	CCCCGTCCTCACCGA[A/C]CCCCGAGGGCACGGC	54472
rs528348842	snp	C/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1291534	TCACCACCCACCCCC[C/T]GAAGGCACGGCCACC	54472
rs528358784	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297149	CTCGGTGTGTCGGAC[A/G]TGAGCTTAGGCAAAG	54472
rs528596551	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306863	CCAGACCCCACACCT[C/G]TCTTTCCGTGCCCTG	54472
rs528630262	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301822	GCTCGTGGCTAAAGG[C/G]ACAGAGGAAGCTAAT	54472
rs528633900	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306261	GGGCTGGCTAGCTTC[A/G]CACGTCCTCTCCACA	54472
rs528682166	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287654	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs528763394	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286677	ATAAGTCACTGCACC[A/G]CTGTCATCTCTAAGT	54472
rs528800054	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290772	GGTCCCGGGACAGAG[C/G]TGAGAGCCAGAGCAT	54472
rs528800382	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286368	AGAGAGGATGGTGAC[A/C]GGAGGGACATCCCAG	54472
rs528847501	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308646	TCAGGAGAGAATTCA[C/G]AGCAGGAAAGGTTCT	54472
rs528881976	snp	C/T	1.65274e-05	0.00287462	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277094	GCATCCTTGTTCCCT[C/T]GCTGGGCTTCCAGCA	54472
rs528885733	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279384	TCCTGGTTACCAAGC[A/G]CGGATGTGTCCATCA	54472
rs528886698	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308119	GACAGCCTGCCCCAG[C/T]CCAGCCTCAGTGAGT	54472
rs528919839	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284311	GAAGCATTCTTTCCT[C/T]GGTGACGGGGTGCAG	54472
rs528927870	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279092	GAAGGGACAGGAGGA[A/G]GGGAACTGCTGCAAA	54472
rs528933100	in-del	-/GAGCACAGGCAGCGTGCGCGGGGCTCAGCGACCAGTGAGGCACA	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1278168	ACCACGAGCAGCCCT[lengthTooLong]GAGCACAGGCAGCGT	54472
rs529162735	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1292480	TCTGCCACACTCAGC[A/G]TCATCCTCTCATTCC	54472
rs529175681	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1287963	CAGCACCATTTTTCA[A/G]TAACAGCCTGAAAAT	54472
rs529210168	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291883	CACGGCTGTCCCGTC[C/T]ACGCCAACCCTCGCC	54472
rs529256302	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297180	TGCACGTGCTGAGGC[C/T]GCCAGAACGCCTCTG	54472
rs529385139	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306288	CACACCTACCCACCC[A/G]GGCCCCTGAAGCTCC	54472
rs529417041	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276182	CCACCACACCCTCTC[A/G]GAATCATGCACAGTG	54472
rs529435647	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301627	GTCAATATCACCCCC[A/G]CATTGAGAACAAGCG	54472
rs529451752	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306915	TCCCATTCCTCCTCC[A/G]AGAGATGTCACGTCC	54472
rs529454471	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278486	CTGCAGGGGTGTAAA[C/T]GGAGCAGACAGGGCT	54472
rs529481463	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273894	GGCAGACACCCCACC[A/G]TGTCCATGGACGCTC	54472
rs529517240	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278169	CCACGAGCAGCCCTG[A/G]GCACAGGCAGCGTGC	54472
rs529614822	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281935	CTCTCCAAGGTCTCC[A/G]CAGACTTCGCCCTTC	54472
rs529676526	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284247	CCTCTAACTCTGAAC[C/G]CCTCAAGGCTGCTTC	54472
rs529695310	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291381	CCCGGGAGCCATCCC[A/G]GCCCTCCCACCCACA	54472
rs529754243	snp	A/C	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1286728	GTGGATAAGTCACTG[A/C]ACTGCTGTCTCCTGA	54472
rs529800311	snp	A/C	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301004	GCAAGCAAGGCTCAA[A/C]GAGTCTCAGCGCTAA	54472
rs529801614	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1295414	CCTACACAGAGCAGA[C/T]GCCCACCTACACCCA	54472
rs529927774	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300741	TGGAGTCCTGAACAC[A/G]TGCAGTCCTGGCCTC	54472
rs529964330	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1305866	CCGCGGTGGCTGCAG[C/T]GGAGTCTCCCGCAAA	54472
rs530063250	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281233	GGCCATGATCATGGC[A/G]TAAAAGCTTTAATAA	54472
rs530098365	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1280857	CAGTGGCTGCAGCCC[A/G]AGTGCCCCTCTGTGC	54472
rs530100385	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1286257	CTGAGTGCACAGGGG[A/G]CGCTGGGCCCTGCTC	54472
rs530137315	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285910	TGACGTCCCCACCCC[A/G]GCGCTCTAAGCCCCG	54472
rs530304635	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289555	CACCCAGTAGGCAGC[C/T]GCACTCTCTGGAAAT	54472
rs530406623	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1294219	GGCTCACAGTGTGTC[A/T]CCTTTCCCTGCATTT	54472
rs530540178	snp	C/T	0.00953873	0.0683987	intron-variant	TOLLIP	GRCh38.p7	11:1291404	CACCCACATGGAGCC[C/T]GCCAGTTCCTCCTTC	54472
rs530571441	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282568	CAACATGGCACACGG[A/G]TACATATGTAACAAA	54472
rs530574150	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296371	CCTATGTCTCCTCGA[A/C]CCTCTGTCCACCACT	54472
rs530613035	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287125	AGCTGTGGATAAGTC[A/G]CTGCACCGCTGTCTT	54472
rs530707621	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1295913	TCCTTATCAAGTCCT[A/G]GACTGTGCTCAGCCT	54472
rs530887663	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281801	CTTGAAACTGTGGGC[A/G]ACACACATGCTCTGG	54472
rs530899999	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306182	TGAAGCATCCCTTAG[A/T]GGCTATTCAGGGAAC	54472
rs530923286	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281333	ATGGTCTGACCTCAG[C/T]GCCCCGGCTTCTGAG	54472
rs531183465	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286290	ACCCCTGCACCACCT[C/T]CTCAAATCCAGGAGG	54472
rs531211166	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304144	GGAAAGCCGGAGGAA[C/G]GGACATCCACTCCCG	54472
rs531257194	in-del	-/C	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1288028	CTCTGCGTCTTGGAG[-/C]CTCTAACTGGCCCTC	54472
rs531285736	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1294415	GTGTCTCCTTTCCCT[A/G]CATTTCTACGAAAGC	54472
rs531405448	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300892	CGGAGCCTTTTTAAA[C/T]CTTCTCACCGTTCCC	54472
rs531426993	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300138	AAATAAAAAGGACAG[A/G]GTAGGGCTCTCATCC	54472
rs531462182	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299886	GCCTCACCAGGAGCC[A/G]GCGGTCCCTGCCGCG	54472
rs531493256	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1294092	TGTCTCCTTTCCCTG[A/C]ATTTCTACGAAAGCC	54472
rs531502298	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311345	CCATGCCTGGACCAA[A/T]CCCTTCCCTGTGAAA	54472
rs531531954	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276844	GGGAGGGGAGCCCCC[A/G]CCCCGTCCTGGACCG	54472
rs531570554	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276482	GCCAGGCCAGAGGCC[A/G]GCCCCACACCATCCA	54472
rs531648699	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279954	GTGGGGACGACCGTC[C/T]AGCTCAGAGACTGTT	54472
rs531658217	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285045	CCAGCACTGGCCTCA[C/T]AGCACTCTCGCCTGC	54472
rs531742987	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299008	AGGGGACAGTCATCG[A/G]AAAACCAGGACAGCC	54472
rs531781590	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289463	ACTCTGCCTCAGAAG[C/T]GCTGCAGGTGCAGCC	54472
rs531827605	snp	C/T	3.42483e-05	0.00413799	intron-variant	TOLLIP	GRCh38.p7	11:1288780	GGAGAAGGCTCTCTG[C/T]GGGAGACAAGAGGGA	54472
rs531893712	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292890	AAGAGCTGCAGGAAG[C/T]GGGAGGAGAACGGCC	54472
rs532022421	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304126	CAGAGGGCCAAAAAC[G/T]AAGGAAAGCCGGAGG	54472
rs532106962	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287626	CCGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs532129211	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1294836	TGTGTCTCCTTTTCC[C/T]GCATTTCTACGAAAG	54472
rs532131811	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305807	GAGCAGCCTGGACAC[A/G]GCACAGCGCACCCAC	54472
rs532166088	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300256	ACTTCAAATTTCTTG[A/G]AATTGCTGATTCTCC	54472
rs532217184	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295354	TGCCGGCGGGGGTCC[A/G]GGAGGTGTCCTTGGG	54472
rs532232106	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1286894	TGCACTGCTGTCTCC[G/T]GAGTTCAAAACTGTC	54472
rs532255815	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300700	CCTTGACAGAGCCCC[A/G]GAAGAGCCCAGCTCA	54472
rs532269566	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1305399	ATGCAGGAAAATCCA[C/T]GGGCTCTTCACAACA	54472
rs532341419	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310931	ACTCCCCATCCAGGA[C/T]ACCATGTGCTCTCAC	54472
rs532419888	snp	C/T	0.00402713	0.0446917	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276858	CGCCCCGTCCTGGAC[C/T]GCCAGGAACCGAAAA	54472
rs532430580	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280498	CGGGAGGGACTGCGC[C/T]GGTGAGGACGTGGGG	54472
rs532451685	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289806	TGGTGAGCGGCCAGA[C/T]GAGTGCCCAGTGGCG	54472
rs532466745	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285537	CAACAGACGCAACAG[C/T]GCAGTAGAGAGCACG	54472
rs532475655	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289489	CAGCCACGGACGGGA[C/T]TCAGGACCCTCAAGG	54472
rs532609674	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289282	GGGGAGAGAAAAGCC[A/G]GGAGGAAAAGGCAGG	54472
rs532643530	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299780	TGCTCACTCGGGCAC[A/G]TGAGCACAGGATGCC	54472
rs532647885	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293437	GGGCTGAGGACCAGA[C/G]CCCTTGGCATCCCAC	54472
rs532714018	snp	G/T	0.000798403	0.0199641	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299057	ACAGTCATGCCCCCA[G/T]CTCAGCGCCACAGCT	54472
rs532749598	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304178	TGCTCAGCAGCCACT[C/T]CAGGAGCCAGGAGAG	54472
rs532871403	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1279518	TGGGCAGAGAGGACG[C/T]CATGGGAGCCCGGGG	54472
rs533016231	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279835	CAGCATGGTAAGTCC[C/T]GGCCGCCGGTGGGCA	54472
rs533043514	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303563	GAAACAGGGCAAGGC[C/T]GGGTGGCAGGGGCAC	54472
rs533051357	in-del	-/ATTTA	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275007	GGAAAGAAGAATCTT[-/ATTTA]ATTAAAGGCCTTGCA	54472
rs533056780	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310131	GGGTGAACGGAACGG[A/G]GATGGAGGCGCTGCC	54472
rs533092073	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309045	CATTAGGGTGCGGGG[C/T]CCTCCTCCATTCGGG	54472
rs533133429	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304466	AAACAAGCGCTGACT[C/G]GAGAGAAGTAACACA	54472
rs533239567	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283950	CTTTCAGGTTGGCCA[C/T]TGGCCTCCAACTCAG	54472
rs533285296	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1292801	CGGCAGACACACAGC[A/G]CAGCAGACGGCGTTA	54472
rs533295828	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302838	CACATCCTCCTCCCA[C/T]GGCCGCTCAGCAGCC	54472
rs533322026	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1292651	GCTGTTCTGGTGCAG[C/G]AGACACTGTGGACAC	54472
rs533409851	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1305762	GACTCCATGGCCAAC[C/G]AGCACCTCCAGAAGC	54472
rs533436410	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276022	CCAAGATGCTACACG[C/T]AGCGCCCAGGCAGTC	54472
rs533465020	snp	C/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1283238	CTCAGCCCTACCCTG[C/G]AAGGCCACGTCAGCA	54472
rs533484841	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297359	CCTCACCTGTGTCCC[C/G]ATCTAAGGCCTGGAG	54472
rs533506541	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288887	TTATCTGTGGAACAG[A/G]GCTCCCACCTGCACC	54472
rs533521258	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279408	TCCATCAAGCCCTCC[A/G]GGAACGGTGAGCGTA	54472
rs533526100	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302239	GCAAGAGGGCGGGAA[C/T]GCGCACCAGGGCTGA	54472
rs533650906	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293039	GCTGCAGGGGCTGAG[C/T]GGGGGCAGTGGGTGG	54472
rs533673944	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307404	TGCCGCTCCCACTTC[C/T]TCATCGCGGGTGTAA	54472
rs533675050	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278203	GGGCTCAGCGACCAG[C/T]GAGGCACAGAGCACA	54472
rs533675688	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298743	CAGCCCCACGCAGCC[C/T]GGGGACCGCAGCCAG	54472
rs533731489	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293485	ACAAGGGGAAGCAGC[A/G]AGGGGACGCAAGCAG	54472
rs533977767	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309318	GTGTGGACGCCGCCG[C/T]TCCCCTCCGGCCGGC	54472
rs534055772	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279530	ACGCCATGGGAGCCC[A/G]GGGCAGCCCAGAGCC	54472
rs534122111	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308299	GATCTGGTCATTACA[A/G]TGTGTGGCACCTCCC	54472
rs534222553	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283995	ACTTCACTAGCCCCA[C/T]GAACTGCACATCACA	54472
rs534258433	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302370	GTGCCAGCCTGCACA[C/T]GCCCCAGGCCTGCAC	54472
rs534263699	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288516	GCCCTGCTGTTTTAT[A/G]GGCTCAGTGCCTCCA	54472
rs534292283	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307448	CGGTGCCCCTCAGAA[C/T]AGGAAGGGCCTGCCT	54472
rs534302346	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288061	GATGCCCCCAGGAGC[G/T]GCAGGTGCCCTGAGA	54472
rs534327214	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307187	ACACCTGAGACCCCC[A/G]TCGCTGACAACACCT	54472
rs534345387	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311463	ATTTCTCTTTCTCCT[A/C/T]GCTGCTATGTCTGCT	54472
rs534388981	snp	C/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1278239	CGTGCGCGGGGCTCG[C/G]CGACCAGCGAGGCAC	54472
rs534448092	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291153	GCAAACAAACTCAAC[A/G]TGGATGGCAGGTTCA	54472
rs534451177	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306518	TGCTTAACCTCCTGC[A/C]TCTCTGGCACCACAG	54472
rs534547188	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297043	GGTTGCTGGTGGAGT[G/T]GGGTGGAGACCCAGC	54472
rs534553641	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287699	CCGCAGCCTCCCCGC[C/T]GCAGCCTCCCCGCTG	54472
rs534581752	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286871	ACTGTCCACTGCAGA[C/T]AAGTCACTGCACTGC	54472
rs534589255	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274625	CTATCTCCGGAGCCC[C/T]GCCTGAGGCTCCAAG	54472
rs534619201	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286568	CTGCGGATAAGTCAC[C/T]GCACCGCTGTCGTCT	54472
rs534619377	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291001	CCCAATCACAAGGAG[C/G]CACATCACATGTAGA	54472
rs534628216	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274139	CACAGAACCACCCAG[A/T]GGGGAGAGGGTGCCT	54472
rs534651271	snp	C/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290519	CCTTTTCCTAACACA[C/G/T]AGACTACAGCCACTC	54472
rs534653364	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295979	GTCCAGCCTGGGGCC[C/T]GGCCCCCAGCGGTAC	54472
rs534716321	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1277921	GTGGGGCAGCAGGTG[C/T]GGTGTACAGTGGACC	54472
rs534737348	snp	A/T			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297764	GGTGCCTGAGCGGAG[A/T]GGGCCCATGCCAGGA	54472
rs534805595	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301149	ATGTATCAAATCACA[C/T]GTAGAAATAAACAAC	54472
rs534930332	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300799	GAGCCGCACCACAGT[C/T]GCCCCTGAAGCACGG	54472
rs534963622	in-del	-/CCCTCTTCCTATCACCCCCTC	0.0228947	0.104514	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302935	GACAGGGCTTTCCTT[-/CCCTCTTCCTATCACCCCCTC]CCCTCTTCCTATCAC	54472
rs535034425	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288315	GCTTGGAAGGGCTGT[A/G]GGGGTCCTCCGAGGA	54472
rs535038230	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308689	GCGCCTATCCTCTCA[C/T]TTGCAAATGAAGAAA	54472
rs535049794	snp	C/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1297494	GGGAAGCTCTCTGCA[C/G]GCTGCACCCCAACCT	54472
rs535049842	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302991	CAAAACACAACAGGC[A/G]CTTCAAAGCCAACAT	54472
rs535118717	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289269	AGCAGGTAGGGACGG[A/G]GAGAGAAAAGCCGGG	54472
rs535173152	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274755	CTGGGCCCTCAGACA[A/C]CAGGGGCCTAAACCC	54472
rs535185803	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278762	ATGACGGAAAACGAA[C/G]CGAACCATGGCCAGG	54472
rs535312492	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1283455	GGACGCCCCTGCTTA[C/T]TGGAAACGCATGCCT	54472
rs535314317	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278339	AAGCACGAACCATCT[A/C]CCAGCTAGGATCACT	54472
rs535349334	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282784	TTAAAGTATAATTAA[A/C]ATAAATAAATAAATA	54472
rs535545314	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274238	AATTCAATCTGGGAA[A/G]CAAAGGCCAGGCTTG	54472
rs535618594	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307264	CGTTTACCGGTCAAC[A/G]GGGGTGCCCCTGAAA	54472
rs535680600	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302907	CCTTGTCTCCCCTTC[C/T]GGGGCCTTCCTCAGA	54472
rs535713830	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289352	CCCCACACTGCTCCC[C/T]GGCCCCCACCCAGTC	54472
rs535802386	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286895	GCACTGCTGTCTCCT[A/G]AGTTCAAAACTGTCC	54472
rs535858349	snp	A/G	1.71422e-05	0.0029276	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290233	CCCTCTCACCTCATC[A/G]AAGATCTCGAGATAG	54472
rs535886968	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299268	GCTTCAGTCCTCCCC[A/G]TACAAATACTGGTTA	54472
rs535942323	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291073	GACATTTGAGGTCCT[C/T]GGGGTGGGAGTGAAC	54472
rs536059960	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300826	ACGGCTGGCCACACG[C/T]AGGCGGCAGGAGACC	54472
rs536156747	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277372	AGGAAGGGGCCACCT[C/T]GGGTCTCAGCAAACA	54472
rs536166702	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300341	TTCCTCCCTCACTGA[C/T]GCCAGAGCTCTAAAC	54472
rs536182091	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293995	TGAAGCCCCTGAAAG[C/G]AAGTCTTATTTGTGA	54472
rs536187965	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305964	CGCACGGTACCCCTC[A/G]CAGGGGCCCCCATGA	54472
rs536245550	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1305125	GCCTTTATCTTCCAA[A/G]AGGCCCGTGGGTCCC	54472
rs536301082	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281478	GGGCTCAGACACCAC[A/G]GGAGGCTCTCGGGGC	54472
rs536339764	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1286429	ACACTGCACTGCTGT[A/G]GTGTCTGAGTTTGAA	54472
rs536351307	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276280	CCCACGGAGCTGGCA[C/T]GAGCGCAGCAGGAGA	54472
rs536407110	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289973	CAGCGGAGGGGACAC[A/G]TGCACGCTGTATCCC	54472
rs536486864	snp	A/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1280284	TCTGGAACTCACAGG[A/C]GCTGCGAACGCCGGC	54472
rs536525462	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1285209	CTTGGCCACTTCCAT[A/G]GCCTGGGCCTCTGGC	54472
rs536536533	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1295053	AGCCTGCGTGGCTCA[C/T]AGTGTGTCTCCTTTC	54472
rs536675686	snp	C/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311540	CACTGGTAACACTTT[C/G]ACTCCTTAACATCGG	54472
rs536682689	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303324	GCAGCAGGCCAAGGG[C/T]GGACAGAGATCCAGA	54472
rs536718031	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276599	CGTCTGGGAAGTTCT[A/G]AAAAAAACCCACAGT	54472
rs536732199	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1282024	GGGCATCAGCTTCCA[A/G]TGAAGAAGGGTGCCT	54472
rs536766490	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286779	GATAAGTCATTGCAC[C/T]GCTGTTGTCTCTGAG	54472
rs536793400	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292986	CAGGACAGTGCCCAC[A/G]AGAAAGGCCCACGCG	54472
rs536980044	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295527	GGTTTCAGGAAAAGC[A/G]GGAATCAGAAGTTCT	54472
rs537016138	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295141	TACAGACGGTTTTCG[G/T]GTGATCAAAATCGGC	54472
rs537022895	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1306400	CTCCCCTTATCACTA[A/G]GGGGAGGCAACGGCT	54472
rs537087337	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287231	GTAAAATCACTGGAG[C/T]GTCATGATGGTTCTG	54472
rs537155268	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276982	ACAGCATTCCTTGGG[A/G]AGCGCCGGGTCGGCG	54472
rs537165221	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281546	CTGCACCCTGTGCGG[G/T]GGTCTCTGGGCAGCG	54472
rs537202234	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1287806	CCCTGCCGCAGCCTC[A/C]CCGCCGCAGCCTCCC	54472
rs537206326	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286452	AGTTTGAAAGTGTCA[A/G]CTTCACATAAGTCAC	54472
rs537292414	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280925	GCCCAGTGGCACCCG[C/T]GCTGGTCTCTCACGC	54472
rs537329822	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280566	GAAATGGAGGTGCAC[A/G]AGGGAACAGATGGAA	54472
rs537375892	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1304985	CTATCGATGGTGCAC[A/G]TGTCTTAAACAAAAG	54472
rs537400118	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285236	TGGCCTCCACCCTCC[A/G]TGCAGAGGGACCAGT	54472
rs537404567	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290946	TGTGCTATCGGAGTA[C/T]GTGGGGTTTTGGGGA	54472
rs537518692	snp	C/T			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311022	CCGGCAGCCTGGCCG[C/T]TTGCCTGTTTTGATG	54472
rs537540709	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289320	CAGGGAGGGCTGGCC[A/G]TCTGCTGGCCTGGCT	54472
rs537573874	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289321	AGGGAGGGCTGGCCG[C/T]CTGCTGGCCTGGCTG	54472
rs537598920	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306715	GCGTGTGCCAGGCAA[C/T]ACTTTACAGAGTGCT	54472
rs537830689	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309712	CTCGCGCGCACGCGC[A/G]CTCCAGGGTAGGGCA	54472
rs537843250	in-del	-/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311387	CCACCCCCTGGCGGC[-/G]GGGGCCCCCCACCGT	54472
rs537972138	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293520	CCACCTGTGTGGCCG[C/G]CCAGAAGCCAAGAGA	54472
rs538006433	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299326	AGAGGCGGCTTGCCT[A/G]CTGCTGCAATGCCCT	54472
rs538043140	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298770	CCAGCGCCATGTGGC[A/G]GGGCAGGTGCGCGTC	54472
rs538048182	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284963	AAGGTGGCCTTTCTG[C/T]ATCTGTGCAGGATGC	54472
rs538050878	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304408	AAATGGAAGGCCCGA[C/G]ACACCAGAAGGGATA	54472
rs538052042	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1307301	CTCGTCTACATGATG[G/T]AAACAGCCCAGGAGG	54472
rs538153901	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292704	TGCCTCCCCCACAAC[A/G]GGCAAGAGACGCACG	54472
rs538330034	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284505	AGGCGCCCACCACCG[C/T]GCCCGGCTAATTTGT	54472
rs538330104	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279261	GGGAGCAGGCACCCC[C/T]GGGGGAAGAGGTGGG	54472
rs538360226	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288834	GGCCACCCTGCCCCT[A/G]CAGCCGCACCATCGT	54472
rs538365239	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1284036	TGACCCCACGACGGC[A/G]GCTCTGGGCTGTCCC	54472
rs538660856	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310315	CGAACAGCGCTGGGT[A/G]AACTGAGGCTGAACC	54472
rs538679105	snp	C/T	3.65384e-05	0.00427409	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286077	GGGGTGGCATCACCA[C/T]GGCAGCTGGAAGCAG	54472
rs538717489	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289954	CGGCCAGACCCTGTG[C/T]GCCCAGCGGAGGGGA	54472
rs538760220	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279638	CACCTGCACGCACGC[A/G]GACGGATGTGCAGCA	54472
rs538797291	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309781	TCCTCGAGCCCTGCA[G/T]CCCGGCGAAATGGCT	54472
rs538920065	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299912	CCGCGAACACATGGA[G/T]ACTCGGGGGACGGAG	54472
rs538925553	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293605	CACCACTGGAGCTGC[A/G]CCACAGAAGGCTGGG	54472
rs538927132	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288856	CACCATCGTGGGCCC[A/G]CCTCGAGTCCCCGTC	54472
rs538964345	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293001	GAGAAAGGCCCACGC[A/G]GGAACGGACCTACTC	54472
rs539001180	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292747	CACCGTGGGGACACA[C/T]GGGCACCGCTGCTTT	54472
rs539018756	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305467	AAGCAACTCTCTCCT[C/T]GAGGTACGGGAAGAT	54472
rs539078513	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306791	CAGGACCCTCCGGCG[A/G]CCTCCAGCTCCTGCC	54472
rs539156782	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275238	GAGCCACATGTGCAC[A/G]CGTGTGGCAGTCTCA	54472
rs539193109	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303060	AACACTAGAATTTGT[A/G]TAAGGGAAGCTGGGA	54472
rs539293205	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279134	TGGCTGTGACGCTGC[A/G]ACGTCACGGCCTGGG	54472
rs539295107	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274861	CACACCTGACACAGG[C/T]GGGGGCGGGGGAGGG	54472
rs539299860	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273991	GGCGCTTTGCTCCCT[A/G]AGCATGAGCCAGTCA	54472
rs539359153	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280115	TGTGATAGTTTGTCT[C/T]GGAAACTTTTAAGCA	54472
rs539372242	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283507	CGGTGGGGCGTCAGG[G/T]GGACGAGTCCTCACA	54472
rs539408853	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1288000	GTTGATGATACAGAC[A/G]AGACGGCAGGAGCTC	54472
rs539495672	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1292449	CGATGCCTGCTCACA[C/T]TGGATCCTGCCTGCT	54472
rs539590395	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302591	ACCAGTACCTGACCC[C/T]GCAGCCCCTGGCACT	54472
rs539612443	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308171	CCCGCCAAATCTCAC[A/G]CTGAATTATGATCCC	54472
rs539651688	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307810	CGTAGGCTCCACACC[C/T]GAGTCTCATAAGTGT	54472
rs539739567	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301728	GTACCCTGAGCCCTA[G/T]GTTTCTCCAGTTCCT	54472
rs539752870	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309006	GGACCATTAGGGTTC[A/C]GGGCCCGCCTCCACC	54472
rs539777312	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287689	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs539779770	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307042	CAGCTGTCCTTATGT[A/G]CTGCCATGTCTACCG	54472
rs539863803	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282982	AAATTGTAAATCCAC[A/T]TTGCTGGGGAAGTCG	54472
rs539957480	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1291673	CCCCGTCCTCGCTGA[C/T]CCCCCGCTGAGGGCA	54472
rs539976105	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288254	GCAGGGCCCAGGGCT[C/G]TATCTCAGACCCTGG	54472
rs539995638	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1296518	AGGTCGCTGATGAGG[C/T]CCTGAGCATGGGTCT	54472
rs540054599	snp	A/C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297647	AGAGAAGCCGTACTG[A/C/T]GAGAACAAGCAGAGC	54472
rs540112009	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274073	CTCTCAGAACGGGGT[C/T]GTGTTCCACGCTCAC	54472
rs540132142	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296159	CCACAGCTAAAGGCA[A/G]GGCCACTGAACTGCA	54472
rs540157336	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301325	CAAAATGTCGACGAT[G/T]CTCATTCAATTCTCC	54472
rs540347173	snp	G/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278435	GGCAGCAGAAGCCAC[G/T]TCAATCCTGGCCTGA	54472
rs540359158	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292769	CGCTGCTTTCCCCAC[A/C]ATGGGCAAGAGATGC	54472
rs540448667	snp	C/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1291821	CCCCGTCCTCACCGA[C/G]CCACCTCTGAGGGCA	54472
rs540512514	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275044	TGTGATTTGTCTATT[-/A]AAAAAAATAAAGCGC	54472
rs540524758	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274956	TAAGCCACTTCTACA[A/G]TAAGCCTTCAAACAG	54472
rs540559420	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1297154	TGTGTCGGACGTGAG[C/T]TTAGGCAAAGTGCAC	54472
rs540572789	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302655	CTCCTGACACTCCCC[A/C]AAACCCACTCCAGCC	54472
rs540609006	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302053	CCTGCTGTGTCTGAG[A/G]GGCTGGCCCTGCCTT	54472
rs540643272	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307340	AAGAGGAGATTCTAA[C/T]GACACCTCAGCACTT	54472
rs540659337	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1307427	GGGTGTAACAGCGCT[A/G]CACGCCGGTGCCCCT	54472
rs540662364	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1278889	GCTTTTTGGGCGCCC[C/T]GGCTGGCAGGCGGGC	54472
rs540736958	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1278123	GCCGGACTTAAGACT[C/T]GCCTCCCAGCCTGGT	54472
rs540773806	snp	A/C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1282440	CAAACCTGCACATTG[A/C/T]GCACATGTACCCTAA	54472
rs540805500	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306077	AGGTACTCACCCATG[C/T]TTTCTGATAATATGC	54472
rs540916557	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1287039	CACTGCACCACTGTC[A/G]CCTCTGAGTTCAAAA	54472
rs540939436	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288550	AAGAGACAAGGGTGT[C/T]TGTGGGGCGGCATAG	54472
rs540943800	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281633	CCCTAAGAAGCCGGG[C/G]TCTCCTTTCCTGGCC	54472
rs540963716	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291365	AGCTGGTGATAGAGA[A/C]CCCGGGAGCCATCCC	54472
rs541002222	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290855	CCTCGCTCTAGGTGA[C/G]AGTGAGGACACCTGC	54472
rs541014711	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1297334	CAAAGGACCCCGAGA[C/G]GGTCTAGCTCCTCAC	54472
rs541021405	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295761	GTGTGGGCGTGATGC[A/G]GAGGAAGTCCTGCGG	54472
rs541021807	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280393	GCGTGTTTTGCTTTC[A/G]TACTTTGTGGACGGG	54472
rs541055438	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299088	GTGAGAGCTGTTCCC[A/G]GGGAGGGGAGCGTCG	54472
rs541114439	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290123	CAGGTGGGGAGCCAC[A/G]CCTCGAAGCCAGCCA	54472
rs541153238	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289821	CGAGTGCCCAGTGGC[A/G]GGGGACACATGCATG	54472
rs541160022	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300966	TGTGCCACGCATGCA[C/T]CTGCACTTGGCATGT	54472
rs541172310	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287582	CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs541203929	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1295169	GGCGTTCAATCTGCC[A/G]ATTTTGGCTTTCACT	54472
rs541331061	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281185	AAATAATACTTTGTT[C/T]AAAAAAATCAAAACT	54472
rs541431951	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291832	CCGACCCACCTCTGA[G/T]GGCACGGCCGCCCCG	54472
rs541557171	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1296181	TGAACTGCAGGTCAC[C/T]TGGTCAAACGAATGA	54472
rs541568331	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296286	AACAGCTGAAATTCA[A/G]AAGTATCCCAGAAGA	54472
rs541588705	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1294175	GGCTCAGTGTGTCTC[C/T]TTTCCCTGCATTTCT	54472
rs541675241	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306741	GTGCTGCGCTGAGCC[A/G]GTAAACTCCAGGGCA	54472
rs541794639	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305259	CAGAGAGAAAGGACT[C/T]GTGAGGAGGCGGTGA	54472
rs541918547	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286612	AAAACTGTCCACTGC[A/G]GATAAGTCACTGCAC	54472
rs541993502	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290658	GACAGCAGAAACCTA[C/T]GACGCTCACAGACAC	54472
rs542130102	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1297421	GTGAGTAAACAGAAG[A/G]GACCCGGACGATCCA	54472
rs542410247	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293939	GGGTCTGAGACACGC[C/T]GCGAGGAAGGGGTGA	54472
rs542450808	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280617	CAGCCACGGTGAGCA[C/T]AGAATGAGCTCATGC	54472
rs542554900	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289729	CTGCTGGTGTGCGGC[A/G]AGACCCTGTGCGCCC	54472
rs542613116	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299646	TCCCGATACATAATG[A/G]ATATTTTTCTAGAAT	54472
rs542624885	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305671	GCAGGAATTATCAAC[A/G]ATGTGAAGAGTGAGG	54472
rs542662628	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311224	CCTTCCTCATTTTCA[C/T]GCTAAAAATCACACC	54472
rs542806608	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285674	TCACCTGACAGGGGC[A/G]TGAGGTTCTCCTGCA	54472
rs542906513	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308600	GCTCTCCTGCAATAT[G/T]AATGCTATAGAAGAA	54472
rs542943394	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285375	CCGCCTGCTAAAGAC[A/G]GCTGGGCCCATCCAT	54472
rs542981238	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293668	GTGGGCTCCAGGGTG[C/T]GGGAGAGGACCAAGG	54472
rs543057589	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305985	GCCCCCATGATACTC[C/T]TCACAGGGGTCCACA	54472
rs543219569	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309905	TCCTCGGTCCTCTGT[C/T]GAGTGGCGACAGGGC	54472
rs543243316	snp	C/T			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310078	TTCTGTTTCACAGGG[C/T]TAAAGATGGGGCGCG	54472
rs543328314	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275231	ACCCACAGAGCCACA[C/T]GTGCACGCGTGTGGC	54472
rs543347600	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286152	ACCCATCAGAACCTC[A/G]GGAATCGCCCTCCCC	54472
rs543404325	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301015	TCAACGAGTCTCAGC[A/G]CTAACGCCAGGTTAG	54472
rs543414100	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1295345	TCCTCCAGCTGCCGG[C/T]GGGGGTCCGGGAGGT	54472
rs543436790	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286717	AACTGTCCACTGTGG[A/G]TAAGTCACTGCACTG	54472
rs543478836	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287615	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs543540489	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1293705	AGAGGCGTGGGCAAC[A/G]CCAGGGCCACCTCCA	54472
rs543542639	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300020	TTCAGGAATGGAACT[C/T]GAGGGAAACAGGCAG	54472
rs543545566	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289468	GCCTCAGAAGCGCTG[A/C]AGGTGCAGCCACGGA	54472
rs543549005	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305751	GCCTCCAGCTGGACT[C/T]CATGGCCAACCAGCA	54472
rs543555900	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1294034	GCGATTCTTCTGCCT[C/G]CTGTATTTGTGCATT	54472
rs543564370	snp	C/T	1.65504e-05	0.00287662	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277148	ATGTTGGGGAACATG[C/T]CCTGGATGGCTTTCA	54472
rs543601149	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281137	CCTACCACGAATTAT[C/T]TGAAATCTGTAAAGT	54472
rs543695091	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276313	CGGACGGCAGCCTCC[A/G]GCGGGCGAAGGACCC	54472
rs543717836	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285758	TCAACTCACCTCATT[C/T]CTGCCAACAATTAGA	54472
rs543729182	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276084	GCTTTTACAGGGCCA[C/T]GCTCGCCAGGCTTTC	54472
rs543755972	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289752	GTGCGCCCAGCGGGG[C/T]GGACACATGCATGCT	54472
rs544003519	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304722	CCTGTACTTTCCCAG[C/G]ACAGTGTGTATGTAC	54472
rs544009171	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1284312	AAGCATTCTTTCCTC[A/G]GTGACGGGGTGCAGG	54472
rs544140985	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310500	CAGATGCTTGCGGAG[A/G]ACAGGCGTTATGCAA	54472
rs544216435	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275324	CTGGACACCGAAGCC[A/C]CCAGCACAGTGAGGC	54472
rs544287679	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302709	CAGTCTCCTGGCACT[A/G]GCATGTTCAATAAAC	54472
rs544391175	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1293162	CCAGCAGCACGAGGG[C/T]TTTGGGCCTCAGCTT	54472
rs544425041	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308000	CCTCCACCACGTCCA[A/G]TACTGGGCTGCGCGA	54472
rs544434926	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288394	GAACACAAACAACCC[C/T]TATGCTGTTTCCCCA	54472
rs544574683	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303239	AGCCTTGCATCCTAA[A/G]TGCTGGGACGGTCAA	54472
rs544612877	snp	C/T	0.0652144	0.168387	intron-variant	TOLLIP	GRCh38.p7	11:1287722	CCCCGCTGCACCCTC[C/T]CTGCCGCAGCCTCCC	54472
rs544649082	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276319	GCAGCCTCCGGCGGG[C/T]GAAGGACCCGGCTTC	54472
rs544736774	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278974	AAGAGGAATGGGGCT[C/T]GGCCATCGCCTGTCC	54472
rs544774343	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283715	AAAGAGGTAAGCCAA[G/T]CAATGTTATCTGTCA	54472
rs544798767	snp	A/C/G	0.00037371	0.0136653	intron-variant	TOLLIP	GRCh38.p7	11:1283594	GTTCCAAAATTTACA[A/C/G]TGTCTATCAAAAGAA	54472
rs544826786	snp	G/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1284850	GTCCTGAACACCAGT[G/T]GACAGCCCAGAGTCT	54472
rs545006977	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304788	TTAATAAATTCAAAA[A/G]GCAATGAGAGAAAAA	54472
rs545019536	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294100	TTCCCTGCATTTCTA[C/T]GAAAGCCCGCGTGGC	54472
rs545064557	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1280332	CCACCGCGTGCACGT[C/T]CTCTATGGGCCTCCC	54472
rs545085068	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298411	GGTGGTCACAGGGAC[G/T]TGTGGGCGTGGGGTC	54472
rs545102838	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285287	CCCCAGAACGAGAGA[A/G]GCCACCTCAGCAGGA	54472
rs545175836	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289355	CACACTGCTCCCCGG[A/C]CCCCACCCAGTCTCT	54472
rs545181396	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308541	CAGTGAGCCAGGAGG[C/T]CACTCACGCCAGGAG	54472
rs545221244	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303332	CCAAGGGCGGACAGA[A/G]ATCCAGAGAGGGACG	54472
rs545221600	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285631	TGGGCGTGAGGTTCG[A/G]ACACGACGGCACAGT	54472
rs545300596	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293937	AAGGGTCTGAGACAC[A/G]CCGCGAGGAAGGGGT	54472
rs545313437	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289002	ACCAGGATGGGCCAG[G/T]GCCAGGGCCAGGGCC	54472
rs545359244	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298895	CAGTCGTCCTCAAAC[C/T]GTCAAGGTCCCAAAA	54472
rs545386472	snp	A/G	0.00835141	0.0640778	intron-variant	TOLLIP	GRCh38.p7	11:1292813	AGCGCAGCAGACGGC[A/G]TTACCACTGCAGGGA	54472
rs545394986	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303847	TCGAGAACAGCCTGG[C/T]CAACATGGTGAAACC	54472
rs545395779	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1283811	AAAAGACAGCCACAG[A/G]GCGCCCGGCCCAGAA	54472
rs545453130	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310512	GAGGACAGGCGTTAT[A/G]CAAAGATTGGCAATC	54472
rs545493272	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290099	CCTGTCATGCACCCA[A/G]TGAAACACCAGGTGG	54472
rs545521245	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291855	CCGCCCCGTCCTCAC[C/T]GACCCCCGAGGGCAC	54472
rs545596358	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287633	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs545654663	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275110	TGGTCATCGGCAAAG[A/G]GTTGCTCTCCCTCCA	54472
rs545657969	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274329	ATTCGTTACTCCTGC[A/G]TATTGTGAATTAAGT	54472
rs545665092	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284099	GGGGGGCAGCCAGGG[C/T]GCATCAGGGCCCCCA	54472
rs545696672	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278364	ATCACTGGAGCGCTA[C/G]AGCCCCAATCTTAGG	54472
rs545697334	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1278999	CTGTCCCTGCCCACA[C/T]GTCTCCCCACAGCGT	54472
rs545834378	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1278062	GAGCAGGAGACGCAC[A/G]GCGGTTCAGCCACTG	54472
rs545918454	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1297605	CGTTTTTGACTGGGA[C/T]ACGTCACGAGTGACC	54472
rs545959896	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1282266	CGCCTGAGGGGGCTC[C/T]CTCTGGCCAAATCTG	54472
rs546165561	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306826	TCCATCCTCGGCCCC[G/T]GGGGCTCCCTCCTCT	54472
rs546168163	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1307282	GGTGCCCCTGAAATA[C/T]CTGCTCGTCTACATG	54472
rs546181019	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302375	AGCCTGCACATGCCC[C/G]AGGCCTGCACACTCA	54472
rs546182601	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308081	TGTTCAGAGCCACTG[C/T]TGATAAAAACTGTAC	54472
rs546218474	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307475	GCCTCCCACTGCTCC[C/T]TGCCTGCTCAGCACC	54472
rs546361616	snp	C/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1287913	ACCCTCTCTGCTGCA[C/G]CCTCTCTGCTGTCAC	54472
rs546400323	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287186	TCACTGCACCACTGT[C/T]GTCTCTGAGTTCGAA	54472
rs546453429	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308422	GAGCAGATGCCGGCA[C/T]CATGCTACCTGTACA	54472
rs546466708	snp	A/G			synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290386	GTCCATGCGGGTCAT[A/G]CCGTAATTCTTGGCC	54472
rs546511315	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290759	GGAAAGAGGAGGAGG[A/T]CCCGGGACAGAGCTG	54472
rs546581631	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1282424	ACGGATACATATGTA[A/G]CAAACCTGCACATTG	54472
rs546783362	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291879	AGGGCACGGCTGTCC[C/T]GTCCACGCCAACCCT	54472
rs546987860	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296013	TGCAGCCCTCACTCA[C/G]GAGATCCCCAAATGC	54472
rs547030760	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301576	CGCCAAACCCCAGAA[G/T]TTTCCTCCCCCAAGA	54472
rs547070701	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301195	AAAAAATATCCTTAG[C/T]GAACTGAAGCTTTTG	54472
rs547117998	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304527	CCCACACAAGGCACA[A/G]CAGCACCCGCGCCAG	54472
rs547181725	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301280	GACATCATTAGCGAT[A/G]GGCTAAATACGTTCT	54472
rs547207914	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306265	TGGCTAGCTTCACAC[A/G]TCCTCTCCACACCTA	54472
rs547215325	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295396	CTGGTGGAAGAGCCA[C/G]GCCCTACACAGAGCA	54472
rs547375214	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311400	GGCGGGGCCCCCCAC[C/T]GTTTTCCTTTCATGG	54472
rs547390476	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286398	GTGTAGGTGTCGAGT[C/T]GGCCTGGGGGGAACC	54472
rs547390607	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276899	CCCAAGAACAGGTGT[A/G]GACGGGGCGGCACAG	54472
rs547512759	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285551	GCGCAGTAGAGAGCA[C/T]GCATCACCCAACAGG	54472
rs547516431	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294791	TGTCTCCTTTTCCTG[C/T]ATTTCTACGAAAGCC	54472
rs547546180	snp	C/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1294854	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG	54472
rs547549555	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289496	GGACGGGACTCAGGA[C/T]CCTCAAGGGTCACGA	54472
rs547584487	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300281	TTCTCCTCCCCCATG[C/T]GCCGCTCTCAGAGGA	54472
rs547596336	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289292	AAGCCGGGAGGAAAA[C/G]GCAGGGCCCAGGCAG	54472
rs547681609	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303009	TCAAAGCCAACATGC[C/T]GGGAGGTTCCCTGGC	54472
rs547859926	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280499	GGGAGGGACTGCGCC[A/G]GTGAGGACGTGGGGG	54472
rs547987390	snp	A/C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295443	CACTACTCATCACTT[A/C/G]AGTTATGTTTGGTAG	54472
rs547999376	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301014	CTCAACGAGTCTCAG[C/T]GCTAACGCCAGGTTA	54472
rs548123948	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300742	GGAGTCCTGAACACA[A/T]GCAGTCCTGGCCTCA	54472
rs548179239	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281943	GGTCTCCGCAGACTT[C/T]GCCCTTCAGCTGGCA	54472
rs548271007	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305887	CTCCCGCAAACGTCC[C/T]GAGATCTCACTGCAG	54472
rs548271786	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281289	TCCCTTCCTCACTGA[A/T]GCGGTCACACTTTAT	54472
rs548307538	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280859	GTGGCTGCAGCCCGA[A/G]TGCCCCTCTGTGCCA	54472
rs548345952	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285921	CCCCGGCGCTCTAAG[C/T]CCCGTTCCCTCCTCC	54472
rs548347428	snp	G/T	1.69069e-05	0.00290743	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290413	GGCCAACTTTGCCTG[G/T]AATGAAGCCAATGTC	54472
rs548372449	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287657	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs548447660	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299870	AGCGCATCGCCACGC[A/G]GCCTCACCAGGAGCC	54472
rs548483815	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301844	GAAGCTAATGAAACA[C/G]AGAGAAATAAATCCC	54472
rs548506591	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289871	ACCTGCTGGTGAGCG[C/G]CCAGATCAGTGCCCA	54472
rs548621386	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311640	CCATTCCTTTAAATG[A/C]CATCCATATGCTGAT	54472
rs548657558	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276938	GGGAGGGGGCGACAC[A/G]GGTGCTCTTTCACGG	54472
rs548686829	snp	C/T			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311008	CTCTCCTTTTAAAAC[C/T]GGCAGCCTGGCCGCT	54472
rs548722050	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1293493	AAGCAGCGAGGGGAC[A/G]CAAGCAGGGAACCAC	54472
rs548824756	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276431	TGCCTTCAGGCCGGA[A/G]TCTGTCACAAGGCTG	54472
rs548868512	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306449	CCCGAGCCAGAGTCC[C/T]GCCCCCGGACCCTGG	54472
rs548908160	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289560	AGTAGGCAGCCGCAC[C/T]CTCTGGAAATCCCAC	54472
rs548944544	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1293806	GGTGGCGGCTGAGGA[C/T]GGGTGATGGCACTGG	54472
rs549006677	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275865	TTACATCCGAAGGCC[A/G]GCGGCAAGACACTTG	54472
rs549052293	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1304851	AAAGAAAACATGTAA[A/C]AAATCTGTAAATCTG	54472
rs549056052	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299293	TGGTTACGCAACCTG[C/T]TGCCCCGCCTACCAG	54472
rs549066879	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276270	TGGGAGGACACCCAC[A/G]GAGCTGGCACGAGCG	54472
rs549081491	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289062	TGGGCTGCTGTCCTC[C/T]TTCAGTTCCACTTCA	54472
rs549144557	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298418	ACAGGGACGTGTGGG[C/T]GTGGGGTCCAGAGGC	54472
rs549183160	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303387	CGCCGGGCACAGGGC[A/G]CGCGCTGCGGCAGCC	54472
rs549190415	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310212	GCTCCGCAGGAGCCC[C/T]GCTCCTCTCCTGCTC	54472
rs549191280	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304288	GGAGTTCCACACACA[C/G]AAAAATAGCTGTCAG	54472
rs549294342	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292697	GCACCGCTGCCTCCC[C/T]CACAACGGGCAAGAG	54472
rs549297613	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279903	CCCTGGGCTCCAGAC[A/G]TCTCGCACCACAGTG	54472
rs549334236	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1285005	GGGTGCTGACCAGGC[C/T]TCTCCACTCCAGCTG	54472
rs549368813	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284437	CACTGCAAGCTCCAC[C/T]TCCTGGGTTCACACC	54472
rs549430326	snp	A/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301558	TGGGGAGGCACACAC[A/G]GCCGCCAAACCCCAG	54472
rs549471946	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1306306	CCCCTGAAGCTCCCT[C/G]TACCCAAGGACAAAA	54472
rs549623004	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302042	TCACCAGCCTCCCTG[C/T]TGTGTCTGAGGGGCT	54472
rs549626625	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310808	ACAACCACTCCACTA[A/T]AAACTCTTTGTCAGT	54472
rs549769561	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289905	GAGGGGACACGTGCA[C/T]GCTCTGTCCCTGGAA	54472
rs549812336	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1294425	TCCCTGCATTTCTAC[A/G]AAAGCCGCGTGGCTC	54472
rs549850842	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305337	CCCAGGAGCAGCCCA[C/T]CAGAGCCAGCGGAGA	54472
rs549860653	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285520	CTAACAGTGACACAC[A/G]ACAACAGACGCAACA	54472
rs549910405	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284265	TCAAGGCTGCTTCTG[C/T]GTTTCTGGCTCACCT	54472
rs549934423	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299888	CTCACCAGGAGCCGG[C/T]GGTCCCTGCCGCGAA	54472
rs550034044	in-del	-/CT	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1291582	CTCTGAGGGCACGGC[-/CT]CACCCTGTCCTCACT	54472
rs550072884	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288848	TGCAGCCGCACCATC[A/G]TGGGCCCGCCTCGAG	54472
rs550077610	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276498	GCCCCACACCATCCA[C/T]AGGAAGCTGCTCAGC	54472
rs550106687	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298460	CACTGTGGGTCCCTC[A/G]CTGCTCTGGATCCTG	54472
rs550113948	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276157	AGCTGTCAGCAGTCG[G/T]CTGGCAGTGCCACCA	54472
rs550152886	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279971	GCTCAGAGACTGTTC[C/T]GGAACTCCCAAGGCT	54472
rs550300369	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285638	GAGGTTCGGACACGA[C/T]GGCACAGTGCAGAGC	54472
rs550315342	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283911	CTTCCAGCCTCAGGA[A/G]GCTGGAGGGCCTGGG	54472
rs550361423	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308139	CCTCAGTGAGTGACA[C/T]GGTTTGAATCTGTGT	54472
rs550452242	snp	G/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1283477	CGCATGCCTGGGCAT[G/T]GGGGCTGGGGGCTCC	54472
rs550484007	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308206	GTTGGAGGTGGGGCC[C/T]GGCAGGGTGGGTGTG	54472
rs550509691	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275688	TTGACAAAAACCACC[C/T]CCAATCGATGGCAGA	54472
rs550534004	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303473	CTCCTGGGATGCTTA[A/C]ACGTGAGTGGAAGAA	54472
rs550570832	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308715	AGAAACTGAGGTTTT[C/G]CACGGTGGCCACTAA	54472
rs550667995	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291895	GTCCACGCCAACCCT[C/T]GCCGCACAGCTGAAC	54472
rs550833164	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287682	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs550844324	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288336	CCTCCGAGGACACAG[G/T]GGCCTGCAGTGGAGA	54472
rs550855114	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273945	GGTGCCAGGGTGGCT[C/T]GGGGTCTCTAGAGTG	54472
rs551041650	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276108	GGCTTTCCTCGCCCA[C/T]GCTGAACCCACGTCC	54472
rs551139886	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302181	AATGGCCCATCCACC[A/C]GATGCCCGCACACCT	54472
rs551140859	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303598	CACTTCCCACAGGGC[A/G]GCAAGGCAGGCCTCA	54472
rs551179565	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301642	ACATTGAGAACAAGC[A/G]TCAAGGACTCCTGAA	54472
rs551279077	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280801	CACCTTCCACCTCAG[C/T]GCCTGTCAGTCTCGT	54472
rs551291767	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278187	ACAGGCAGCGTGCGC[A/G]GGGCTCAGCGACCAG	54472
rs551328831	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1277831	ACCTCAGCAAAGCTG[C/T]AGCCGATGCCCAGAA	54472
rs551330441	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282538	TTAAATGATGAGTCA[A/G]TGGGTCCGGCACACC	54472
rs551331757	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299126	GACATGGGTGAGACA[C/T]ACAGGACCTCTTCGT	54472
rs551376139	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279137	CTGTGACGCTGCGAC[A/G]TCACGGCCTGGGGTG	54472
rs551410231	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304211	CGGGGTCCCACCTTC[A/G]AGGCACTGAGGACAA	54472
rs551414712	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1283957	GTTGGCCATTGGCCT[C/T]CAACTCAGGACAACC	54472
rs551423521	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311225	CTTCCTCATTTTCAC[A/G]CTAAAAATCACACCT	54472
rs551462416	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290963	TGGGGTTTTGGGGAC[A/T]GGAACTTGTCTTTCT	54472
rs551505193	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279519	GGGCAGAGAGGACGC[C/T]ATGGGAGCCCGGGGC	54472
rs551618843	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307437	GCGCTGCACGCCGGT[A/G]CCCCTCAGAACAGGA	54472
rs551640536	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284418	CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC	54472
rs551670252	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297372	CCCATCTAAGGCCTG[A/G]AGCGCACAAGCCAGT	54472
rs551711620	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302241	AAGAGGGCGGGAACG[C/T]GCACCAGGGCTGAGA	54472
rs551787135	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281232	GGGCCATGATCATGG[C/T]GTAAAAGCTTTAATA	54472
rs551800273	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292670	CACTGTGGACACCGT[A/G]GGGACACACGGGCAC	54472
rs551899938	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297740	ACGGACAATCGAGGA[A/G]GGTGCAGAGGTGCCT	54472
rs551955606	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290947	GTGCTATCGGAGTAC[A/G]TGGGGTTTTGGGGAC	54472
rs551963781	snp	A/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1296381	CTCGACCCTCTGTCC[A/C]CCACTGCCACTTCTG	54472
rs552013809	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287126	GCTGTGGATAAGTCA[C/G]TGCACCGCTGTCTTC	54472
rs552100447	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295967	GGGGTCAAGGGTGTC[C/T]AGCCTGGGGCCTGGC	54472
rs552106761	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283300	TAGGAGCAAGATGGG[A/G]ACCCCTCCAGGCCAA	54472
rs552154114	snp	A/C	0.00358779	0.0422022	intron-variant	TOLLIP	GRCh38.p7	11:1278228	AGCACAGGCAGCGTG[A/C]GCGGGGCTCGGCGAC	54472
rs552192675	snp	C/T	0.00438332	0.0466095	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299816	CTGCGTCACCTGTGC[C/T]GTCAAAACGCCCCGT	54472
rs552233059	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277685	TACACGGAATGTCAC[A/G]CCCGCTGATCCAAAC	54472
rs552271777	snp	A/C/T	0.000218629	0.0104532	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277245	CGGGGCTACAGACAG[A/C/T]GGGCATCCCTGGAAG	54472
rs552283135	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280013	CTCACTCCACAGAGC[A/G]TTATCACAAAGAAGA	54472
rs552313994	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286826	GTGGATAAGTCACTG[A/C]ACTGCTGTCGTCTCT	54472
rs552488563	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1284746	AGCCCTGGCACCTGC[A/G]CGGGCGGCTTCACAT	54472
rs552565803	snp	A/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300796	AAGGAGCCGCACCAC[A/T]GTCGCCCCTGAAGCA	54472
rs552586603	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286297	CACCACCTCCTCAAA[A/T]CCAGGAGGTGACATG	54472
rs552600543	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1305950	TCCTCGCGGGGGCCC[A/G]CACGGTACCCCTCGC	54472
rs552618102	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307256	TTACTATGCGTTTAC[C/T]GGTCAACGGGGGTGC	54472
rs552618343	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301437	CAGCAGGTCTGAGAT[C/T]GCACATGTGTCGCGG	54472
rs552686376	snp	G/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1297049	TGGTGGAGTGGGGTG[G/T]AGACCCAGCCGTCTG	54472
rs552760853	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282130	GGAACCAGGGCTCCT[A/G]GGAGAAACAGCTAAC	54472
rs552767639	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1286955	TCTCTGAGTTCAAAA[C/T]TGTCAACTGTGGATA	54472
rs552866388	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277957	TGCACTGGGGCCACC[A/G]TCCAGGGTTCCTGGC	54472
rs552894464	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1286878	ACTGCAGATAAGTCA[C/T]TGCACTGCTGTCTCC	54472
rs552910136	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287825	CCGCAGCCTCCCCGC[C/T]GCACCCTCCCCGCCG	54472
rs552932974	snp	C/T	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1286573	GATAAGTCACTGCAC[C/T]GCTGTCGTCTCTGAG	54472
rs552971763	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290551	GAGTCGCCTGAACAC[A/G]GCTGTGACCTGCTTC	54472
rs553069556	snp	A/C	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1278252	CGGCGACCAGCGAGG[A/C]ACAGAGCTCCTCCTG	54472
rs553200168	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1278225	CAGAGCACAGGCAGC[A/G]TGCGCGGGGCTCGGC	54472
rs553277901	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281655	TTCCTGGCCCACTCC[C/G]GCAGCCCCGTCTCAC	54472
rs553523460	snp	A/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1295170	GCGTTCAATCTGCCG[A/T]TTTTGGCTTTCACTT	54472
rs553595738	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300812	GTCGCCCCTGAAGCA[C/T]GGCTGGCCACACGCA	54472
rs553633772	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305955	GCGGGGGCCCGCACG[A/G]TACCCCTCGCAGGGG	54472
rs553672351	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305616	AAGTGATAAAGTTCA[A/G]AAACTACCCTCTGCC	54472
rs553698556	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276767	TTTTCCAGAACGGCA[C/T]GAGAAGGAGAGACGC	54472
rs553699616	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293963	GGGGTGACGGTGTAG[C/T]TGTGCTCACCACACC	54472
rs553736203	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299944	CGGAGGCGGAGGTGC[C/G]GCACGACCTGCTGCA	54472
rs553779754	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304546	CACCCGCGCCAGGAC[A/G]GGGCGGCCGAGGTCT	54472
rs553818470	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310319	CAGCGCTGGGTAAAC[C/T]GAGGCTGAACCCCGC	54472
rs553846050	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311138	TTAACCACAAGTTCC[C/T]GCTTTGGGGGCCTAG	54472
rs553994224	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293623	ACAGAAGGCTGGGTG[A/G]GCTCACGTGGAGGAA	54472
rs554075740	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291289	TCCTGCCTGGAATGC[A/T]GACGGCCTCCCTGTA	54472
rs554094100	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288860	ATCGTGGGCCCGCCT[C/T]GAGTCCCCGTCTTAT	54472
rs554216025	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284103	GGCAGCCAGGGCGCA[A/T]CAGGGCCCCCAGGGC	54472
rs554303873	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276226	CTCTCACCCCAGCCT[C/T]GCAAGGCCTGTTGAG	54472
rs554473822	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290003	CTGGGTCATGCTTGT[C/G]ACTGGGGATGTTTCC	54472
rs554555070	snp	A/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311496	TCTCTCTTTATTTCT[A/G]TCCTGGGAGATTACA	54472
rs554562384	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299999	GACACCAACTCTGGA[A/G]GAGCATTCAGGAATG	54472
rs554603093	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305140	GAGGCCCGTGGGTCC[C/T]CACACAGTGAAAAGA	54472
rs554604897	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293770	GGTGGAGTGCCCTGC[A/G]GTCACCAGGCCCTGC	54472
rs554690956	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1296039	AATGCAGGTTTCTGC[C/T]GCTAAAAATGGGTTC	54472
rs554695326	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286437	CTGCTGTGGTGTCTG[A/G]GTTTGAAAGTGTCAA	54472
rs554735172	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281052	CATGAGGCCACGCGG[G/T]CTCCAGATGCTTCAC	54472
rs554750390	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280285	CTGGAACTCACAGGC[A/G]CTGCGAACGCCGGCT	54472
rs554790585	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287703	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCTGCACC	54472
rs554889315	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285226	CCTGGGCCTCTGGCC[G/T]CCACCCTCCGTGCAG	54472
rs554891669	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289738	TGCGGCAAGACCCTG[C/T]GCGCCCAGCGGGGCG	54472
rs554926060	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284703	GCCCTCTCAGACACA[C/T]GCTCTGCTCTTTCCT	54472
rs554947163	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287584	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs555002842	in-del	-/ACA	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1307194	AGACCCCCGTCGCTG[-/ACA]ACACCTTCTTAAGAG	54472
rs555117751	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276284	CGGAGCTGGCACGAG[C/T]GCAGCAGGAGAGACG	54472
rs555138738	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300391	ACACGAAAGAAAAGA[C/G]GTCTCCAACATTCAC	54472
rs555177063	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310418	CCCGGAACTTAGGTC[C/T]CGATGTCCGGGTATC	54472
rs555217638	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1285153	TCCCCTAACACCACC[A/T]CCCCCAACACCACCA	54472
rs555343358	snp	A/C	0.00993419	0.0697739	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274520	GCGCACGTTCTGAGA[A/C]CACTCCTGCCTGGCA	54472
rs555449722	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274974	AGCCTTCAAACAGGA[A/G]ATAAAGCATAAAATG	54472
rs555594025	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298750	ACGCAGCCCGGGGAC[C/T]GCAGCCAGCGCCATG	54472
rs555620261	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298264	GGCAGACAGACAGGC[A/G]GCTCGTGCCCTCCTG	54472
rs555702183	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279226	GAATCCCAACAGCAC[A/G]GCCCCAACACACTCA	54472
rs555703479	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280296	AGGCGCTGCGAACGC[C/T]GGCTGCTCCCGTGCA	54472
rs555717418	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299342	CTGCTGCAATGCCCT[C/T]GTTTCTCAACTTAGA	54472
rs555728598	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308316	GTGTGGCACCTCCCC[A/C]CCCCCAACTCTCTTG	54472
rs555741554	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291782	CGCCCCGTCCTCACC[A/G]ACCCACCTCTGAGGG	54472
rs555805718	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1284030	GCACTTTGACCCCAC[A/G]ACGGCGGCTCTGGGC	54472
rs555851304	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285629	AATGGGCGTGAGGTT[C/T]GGACACGACGGCACA	54472
rs555948045	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292083	TTGGGTGGCCACAGC[A/G]TACTCCGGAATGCTA	54472
rs555981510	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288101	GCTGGGAGCCAGGGC[A/G]CTGACGTGCTGGCCC	54472
rs555985041	in-del	-/TGAA	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1291585	TGAGGGCACGGCCAC[-/TGAA]CCTGTCCTCACTGAA	54472
rs556016353	snp	C/G	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1287409	TGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs556065834	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1296517	AAGGTCGCTGATGAG[A/G]CCCTGAGCATGGGTC	54472
rs556124494	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285245	CCCTCCGTGCAGAGG[G/T]ACCAGTGCTCTGCCT	54472
rs556143806	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304481	CGAGAGAAGTAACAC[A/C]TTCCTGCGGGAGCCC	54472
rs556371533	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1293546	AGAGAAGCAGGAAAC[A/G]GGGGCTGAGCTACCT	54472
rs556458938	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298794	GCGCGTCCAGCTCCC[C/T]GAGATGACACACGCC	54472
rs556480767	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1292728	ACGCACGTCAGACAG[C/T]AGACACCGTGGGGAC	54472
rs556555945	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309731	CAGGGTAGGGCAGGC[A/G]CAGCCTCTCGCCCGG	54472
rs556560821	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297590	CCCCACACTTTACCC[C/T]GTTTTTGACTGGGAC	54472
rs556683286	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275475	GCGTAAGACCAGGCC[A/G]TCTGAGACAGGGAAT	54472
rs556685120	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1284048	GGCGGCTCTGGGCTG[C/T]CCCAGTTACAAATCA	54472
rs556726215	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279263	GAGCAGGCACCCCCG[A/G]GGGAAGAGGTGGGTG	54472
rs556779345	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279569	GCGGCCCTGGGAGGA[A/G]TGATGGGCGGCTTTG	54472
rs556829531	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278342	CACGAACCATCTCCC[A/G]GCTAGGATCACTGGA	54472
rs556830893	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274319	ATTCTGACTGATTCG[G/T]TACTCCTGCGTATTG	54472
rs556905095	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282260	AGATCCCGCCTGAGG[A/G]GGCTCCCTCTGGCCA	54472
rs556942702	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1277477	AGGGCCCTCTGTGAC[A/G]CCTCCTTCACTAACT	54472
rs556977898	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302515	CTGCAATTCCCCATG[C/T]CCACTCAGCTGCTGG	54472
rs557034755	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274831	GCCTGTCCTTCTGAG[A/T]GTGACGACCTCATCC	54472
rs557039943	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285569	ATCACCCAACAGGAG[C/T]GTGAGGTTCAGACAC	54472
rs557043840	snp	A/G	0.000152748	0.00873789	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290244	CATCGAAGATCTCGA[A/G]ATAGAAAGAGTCCAC	54472
rs557216717	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291164	CAACATGGATGGCAG[G/T]TTCAAATATAAAACC	54472
rs557259141	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287731	ACCCTCTCTGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs557395003	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298495	TCCCGGTATTTGAAG[A/G]CGTCCAGCGCTCCAT	54472
rs557438030	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306870	CCACACCTCTCTTTC[C/T]GTGCCCTGCCCTCCC	54472
rs557589005	snp	A/G	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1306343	TCCCAGGACCCCATT[A/G]GCGGCCCCTCTGCTC	54472
rs557609742	snp	C/T	0.000111262	0.00745777	intron-variant	TOLLIP	GRCh38.p7	11:1295603	CCCACCCCCACCGAG[C/T]GCACCAGCCCCAGGC	54472
rs557646504	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300862	TTCCTGGCCACTTCC[A/G]TGACTGGCCCCCTGC	54472
rs557877206	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1283060	GTGCCTCCCACACAG[A/G]ACATATTTTAGTTCC	54472
rs557923691	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303078	AGGGAAGCTGGGAGA[C/T]GACAGTATTGAAACG	54472
rs557959830	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1292686	GGGACACACGGGCAC[C/T]GCTGCCTCCCCCACA	54472
rs558008584	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308189	GAATTATGATCCCCA[A/G]TGTTGGAGGTGGGGC	54472
rs558047767	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307822	ACCTGAGTCTCATAA[C/G]TGTCAGGAGGTTTCC	54472
rs558059713	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278884	CCGTGGCTTTTTGGG[C/T]GCCCCGGCTGGCAGG	54472
rs558086205	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309390	GCCAGCCGCAGCTGA[A/G]CAGTAGCCCTGACCC	54472
rs558118456	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296164	GCTAAAGGCAGGGCC[A/C]CTGAACTGCAGGTCA	54472
rs558184727	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1288051	TGGCCCTCCTGATGC[C/T]CCCAGGAGCTGCAGG	54472
rs558310834	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1288468	CTGCCACCAAACCAC[C/G]CAGGGCCCCTGCCCT	54472
rs558344097	snp	A/G	0.0352966	0.128072	intron-variant	TOLLIP	GRCh38.p7	11:1296674	GGCCTGGTTGCTGGT[A/G]GAGTGGGGTGGAGGC	54472
rs558370274	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1291698	AGGGCACGGCCGCCC[C/T]GTCCTCGCTGACCCC	54472
rs558381109	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301782	CTTTCAGAGCTGGGA[C/T]CCACAGCAGGAAGAC	54472
rs558408762	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1291336	TCCTGCAGCCAACCC[A/G]GCTCACCCCCAGGAG	54472
rs558432579	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281571	GCAGCGATCAGCAGG[A/C]GACAGCTGAATGAAC	54472
rs558503708	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290116	GAAACACCAGGTGGG[A/G]AGCCACGCCTCGAAG	54472
rs558515225	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295532	CAGGAAAAGCGGGAA[G/T]CAGAAGTTCTGTTTG	54472
rs558617412	snp	A/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298822	GCCTCACATCTGGGT[A/T]TTCTTCCCAAAAACC	54472
rs558643762	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282039	GTGAAGAAGGGTGCC[C/T]TATTCACACTCTACA	54472
rs558673429	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277894	AAGAAAATGCTCACA[A/G]AACTCAAACAAGTGG	54472
rs558712141	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1277501	ACTAACTCATCTTCC[C/T]TCCATATAAAAATCA	54472
rs558847993	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280587	ACAGATGGAAACAGC[A/G]TCAACGGGCAGCTGC	54472
rs558851364	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1286159	AGAACCTCGGGAATC[A/G]CCCTCCCCACAATTG	54472
rs558882693	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305570	GGGAAAGCTAATCTT[C/T]ACAAACAATCCCAGT	54472
rs558949290	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280294	ACAGGCGCTGCGAAC[A/G]CCGGCTGCTCCCGTG	54472
rs559027121	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1280174	CGTATTTTAAATGGC[-/A]ATGTGCTGCTCAGCT	54472
rs559096159	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300093	AGTTATTTTTAGAAA[C/G]TTTTTAAAAACATTC	54472
rs559117125	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300993	ATGTAAACACTGCAA[A/G]CAAGGCTCAACGAGT	54472
rs559193349	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305855	CTCTGACGGCACCGC[A/G]GTGGCTGCAGCGGAG	54472
rs559331392	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296191	GTCACTTGGTCAAAC[A/G]AATGAGACAAAAGCT	54472
rs559359429	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287638	CCCCGCCGCAGCCTC[C/T]CCGCCGCACCCTCCC	54472
rs559380216	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290128	GGGGAGCCACGCCTC[A/G]AAGCCAGCCAGGAAC	54472
rs559470168	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281216	TAAAACTGTTCTCTT[C/T]GGGCCATGATCATGG	54472
rs559515062	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289831	GTGGCGGGGGACACA[G/T]GCATGCTCTGTCCCT	54472
rs559718623	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280814	AGCGCCTGTCAGTCT[C/T]GTGGGGACCCTCAGG	54472
rs559763873	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300106	AACTTTTTAAAAACA[C/T]TCGTGAATTACTTTT	54472
rs559830456	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299858	GCACATCCACCCAGC[A/G]CATCGCCACGCGGCC	54472
rs559899229	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276328	GGCGGGCGAAGGACC[C/T]GGCTTCAGATGCCCG	54472
rs560039218	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280374	CCAGCAGCGGCGTCC[A/G]CCTGCGTGTTTTGCT	54472
rs560048232	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290416	CAACTTTGCCTGGAA[G/T]GAAGCCAATGTCAGG	54472
rs560268071	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310637	CTCCTCGTGCTTTTG[A/G]GAACACCCTGCTCTA	54472
rs560277476	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279843	TAAGTCCCGGCCGCC[A/G]GTGGGCAGGGGAGCA	54472
rs560282749	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293208	GCCACCTGCGGACAC[A/G]GGGGAGAAGCCGGGA	54472
rs560298483	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310151	GAGGCGCTGCCAGAA[A/G]AGCCCGAGCTCGAGC	54472
rs560313521	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298914	AAGGTCCCAAAAACA[C/T]AAGGAAAGCCTGAGA	54472
rs560357534	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308553	AGGCCACTCACGCCA[G/T]GAGCCCATCATCTCT	54472
rs560376118	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285332	ACAGGCTCCCCCCTA[C/G]CACCTCCTCTCAGGG	54472
rs560409021	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284941	CTAGGGCGAGGTCCC[A/G]ACTCCCAAGGTGGCC	54472
rs560473227	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297447	ATCCAGGCACCGCTT[C/T]GAGCAGTTACGGACT	54472
rs560531584	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279288	TGGGTGCTTCCACGG[C/T]GTGGGCTGAGGGGCA	54472
rs560639925	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275560	TTCTTCTTCAAAGGA[A/T]CAAAGGCCTTTAGGA	54472
rs560664704	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285621	CGTCACCCAATGGGC[A/G]TGAGGTTCGGACACG	54472
rs560848172	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276791	GAGACGCACGTCCCA[A/G]GGACAGGAGAGCGCG	54472
rs560889833	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279000	TGTCCCTGCCCACAC[A/G]TCTCCCCACAGCGTG	54472
rs560901278	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300125	TGAATTACTTTTAAA[A/G]TAAAAAGGACAGGGT	54472
rs561142828	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293678	GGGTGCGGGAGAGGA[C/T]CAAGGGGGGCCAGAG	54472
rs561181955	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298431	GGCGTGGGGTCCAGA[A/G]GCCTCTGAGGGAGCA	54472
rs561184653	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310749	CTTCCACAAGATCCA[C/T]GAATCCTCTTTTGGG	54472
rs561187706	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1278843	AGGCTTGGGCGCTGT[C/G]TGTCCTGGAGGGACC	54472
rs561219579	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303388	GCCGGGCACAGGGCG[C/T]GCGCTGCGGCAGCCT	54472
rs561246731	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285016	AGGCCTCTCCACTCC[A/G]GCTGGGCTGGACACC	54472
rs561351011	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289248	TCTGAGGGCCAGGGA[A/G]GGGAAAGCAGGTAGG	54472
rs561387548	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293336	GGGTGGAGCTGAGTG[G/T]TCGGCTCAGGCTGGG	54472
rs561480784	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280436	GGTCTGGTTGGCTCC[A/G]CAGAAACCAGTGGGG	54472
rs561653438	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275677	CAACAGTATATTTGA[A/C]AAAAACCACCCCCAA	54472
rs561789162	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1291880	GGGCACGGCTGTCCC[A/G]TCCACGCCAACCCTC	54472
rs561932224	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297170	TTAGGCAAAGTGCAC[A/G]TGCTGAGGCCGCCAG	54472
rs561937551	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306336	AGAACCCTCCCAGGA[C/T]CCCATTAGCGGCCCC	54472
rs561965756	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287759	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs562077799	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287661	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs562123605	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274507	AAAATAATCAGAAGC[A/G]CACGTTCTGAGACCA	54472
rs562134018	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1307350	TCTAACGACACCTCA[A/G]CACTTGCCAGCACAG	54472
rs562145806	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1279789	CCATTCAGGAAAAAT[C/T]GCTCCGAGAAGGCCC	54472
rs562252019	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283118	TGAGGGACGAGCAAG[C/T]CACACCACTAGCCCT	54472
rs562288112	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1282474	TTAAAGTATAATTAA[A/G]ATAAATAAATAAATA	54472
rs562322023	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1280696	CCCACTTTCCAGGCC[A/G]ATTCTCCTCCCACCA	54472
rs562484322	snp	A/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1284760	CGCGGGCGGCTTCAC[A/T]TGGAAACAGAGTCTA	54472
rs562486467	in-del	-/C	0.0221141	0.102801	intron-variant	TOLLIP	GRCh38.p7	11:1294429	GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG	54472
rs562518688	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288968	ATCAGCCTCCGTAGG[G/T]GACTTCTTCCCTCTC	54472
rs562675977	snp	A/C			intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295680	GTCGGCCCACGGTGC[A/C]CACTGCGCCTCCGTA	54472
rs562680118	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284323	CCTCGGTGACGGGGT[A/G]CAGGTGCTACCTCTG	54472
rs562779947	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303267	CAAGCAAGGCAGAGG[C/T]GGAAAACCCCTTCTC	54472
rs562857927	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292649	ATGCTGTTCTGGTGC[A/G]GGAGACACTGTGGAC	54472
rs562870147	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298369	CCGGAGACAGCAGCA[C/T]GGAGAAGCCAGTCGG	54472
rs562890069	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289939	CCACCTGCTGGTGAG[C/T]GGCCAGACCCTGTGC	54472
rs562942040	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1283755	TCTTTCAGCCAGATA[C/T]ACCCTGGCGCTGTAT	54472
rs562959840	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1291833	CGACCCACCTCTGAG[A/G]GCACGGCCGCCCCGT	54472
rs562973418	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302782	GCAAGGCAGCTCCCA[C/T]GCCAGTGTGGACGGG	54472
rs563033782	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278981	ATGGGGCTCGGCCAT[C/T]GCCTGTCCCTGCCCA	54472
rs563041747	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310283	GGTCAGGCGCTCCAA[C/T]CAGAGCGACTCCAGC	54472
rs563141755	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296368	CATCCTATGTCTCCT[C/T]GACCCTCTGTCCACC	54472
rs563153436	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1287088	TCACTGCACCGCTGC[C/T]GTCTCTGAGTTCAAA	54472
rs563178913	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295854	CACAAAGCAGCCCGA[C/G]AGCAGCTGCCCCCGG	54472
rs563180581	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301474	GAGAACTCCGTATCC[A/G]TGTGCTGGGACACCC	54472
rs563188512	snp	A/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1291397	GCCCTCCCACCCACA[A/T]GGAGCCCGCCAGTTC	54472
rs563213511	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1283222	AGCAGCCCCGGGGAA[A/G]CTCAGCCCTACCCTG	54472
rs563254846	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287619	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs563272989	snp	C/T	0.0295035	0.117819	intron-variant	TOLLIP	GRCh38.p7	11:1287724	CCGCTGCACCCTCTC[C/T]GCCGCAGCCTCCCCG	54472
rs563273616	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278046	TGAGATGCAATCTAT[C/T]GAGCAGGAGACGCAC	54472
rs563331851	in-del	-/GGGGCCCGCACGGTACCCCTCGCA	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305943	TCGATACTCCTCGCG[-/GGGGCCCGCACGGTACCCCTCGCA]GGGGCCCCCATGATA	54472
rs563351183	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299672	AGAATTTTGCTTCCA[C/T]GTACAAGATGCACAT	54472
rs563445811	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306177	AGGGCTGAAGCATCC[C/T]TTAGTGGCTATTCAG	54472
rs563483445	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1281292	CTTCCTCACTGATGC[C/G]GTCACACTTTATTTT	54472
rs563571473	snp	C/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1306752	AGCCGGTAAACTCCA[C/G]GGCAAGTCCAGTCCT	54472
rs563745360	snp	C/T	0.000175649	0.00936983	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290190	AGCCACGCTCAGCCA[C/T]GTGCAGCCTCCATAA	54472
rs563799027	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287870	CACCCTCTCTGCTGC[A/G]GCCTCCCTGCTGCAC	54472
rs563846965	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286622	ACTGCGGATAAGTCA[C/T]TGCACTGCTGTCTCC	54472
rs563884078	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290683	AGACACAGCTGAGGC[C/T]GCCACTCACCCACCA	54472
rs563931387	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295259	GGAGGGAGGGTGCAG[A/G]CACCGGCACTGAGGC	54472
rs563936435	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1291856	CGCCCCGTCCTCACC[A/G]ACCCCCGAGGGCACG	54472
rs563937850	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299924	GGAGACTCGGGGGAC[A/G]GAGGCGGAGGCGGAG	54472
rs564149597	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278064	GCAGGAGACGCACGG[C/T]GGTTCAGCCACTGCA	54472
rs564228563	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301564	GGCACACACGGCCGC[C/T]AAACCCCAGAAGTTT	54472
rs564249862	in-del	-/A	0.00478085	0.0486577	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298691	TGTGGATAGAACACG[-/A]AAAGGGGAGAAGCAG	54472
rs564289063	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277688	ACGGAATGTCACGCC[C/T]GCTGATCCAAACACT	54472
rs564332740	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297145	AACCCTCGGTGTGTC[A/G]GACGTGAGCTTAGGC	54472
rs564506933	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281824	TGCTCTGGCCAAGAT[A/G]CACTTTGAGATTCCA	54472
rs564731895	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290763	AGAGGAGGAGGTCCC[A/G]GGACAGAGCTGAGAG	54472
rs564752868	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287769	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs564830181	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305802	AGTCAGAGCAGCCTG[C/G]ACACGGCACAGCGCA	54472
rs564901568	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295353	CTGCCGGCGGGGGTC[C/T]GGGAGGTGTCCTTGG	54472
rs564921164	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300888	CCTGCGGAGCCTTTT[C/T]AAACCTTCTCACCGT	54472
rs564988956	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1294073	AGCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs564992906	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280942	CTGGTCTCTCACGCA[C/T]GAAGAACGCACGGGA	54472
rs565072163	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280729	AAGCAGAAGGAGGTG[A/G]AAAGCAACAGGAGGA	54472
rs565076561	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276852	AGCCCCCGCCCCGTC[C/T]TGGACCGCCAGGAAC	54472
rs565090520	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281169	TCTAATTTGGTAATC[A/G]AAATAATACTTTGTT	54472
rs565110837	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285786	AGAAAAAAAAAAAAA[A/C]AACAATTCTATTTTC	54472
rs565136476	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293742	AGCCAGCTCTGGAGC[C/T]TGAACTGTGTGAGGT	54472
rs565137947	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1297086	CCCCGGTCAGCGCCA[A/G]TGCCCTGGGCAGTTG	54472
rs565186566	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290144	AAGCCAGCCAGGAAC[A/G]TGGCTGTGTTGGCAG	54472
rs565222404	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1283620	AAGAAAATTTCAAAG[C/T]TTGTCTAGCCTTTCC	54472
rs565268053	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276315	GACGGCAGCCTCCGG[C/T]GGGCGAAGGACCCGG	54472
rs565303601	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285529	ACACACGACAACAGA[C/T]GCAACAGCGCAGTAG	54472
rs565404526	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304730	TTCCCAGCACAGTGT[G/T]TATGTACTTGAGATA	54472
rs565536966	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299045	AACCTGGAGCCAACA[A/G]TCATGCCCCCAGCTC	54472
rs565573483	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304161	GACATCCACTCCCGG[G/T]CTGCTCAGCAGCCAC	54472
rs565608802	snp	A/C	0	0	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300316	GACGCAAGCCTGTGA[A/C]TGACGACCATTCCTC	54472
rs565643461	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305450	CACACATCTACAAAG[A/G]AAAGCAACTCTCTCC	54472
rs565735378	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286117	AGCGGAGATGGTCCC[A/G]GGGTCAAGGAGGAAC	54472
rs565780686	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305085	TGGCCATGCCAGTAT[C/G]AGACAAAATAATCAA	54472
rs565889600	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302619	ACTCCAGCCAGCCTC[A/G]GCCTCACGCTCCACA	54472
rs565950482	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1295867	GACAGCAGCTGCCCC[C/T]GGCATTCCCGCGGCC	54472
rs565965293	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289518	GGGTCACGACCATTC[A/G]CACCACCAAGAACAG	54472
rs565965390	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285201	GCCCGCAACTTGGCC[A/G]CTTCCATGGCCTGGG	54472
rs565974282	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299966	CCTGCTGCAGGGAGC[C/T]ATAAGGAGGCCTCTG	54472
rs565999518	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280508	TGCGCCGGTGAGGAC[A/G]TGGGGGCAGCAGAGA	54472
rs566071757	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306927	TCCGAGAGATGTCAC[A/G]TCCTCACCCCAACAC	54472
rs566100657	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306951	CCAACACCCAGCCCT[A/G]GTGAGGCCCATTTAC	54472
rs566111071	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311401	GCGGGGCCCCCCACC[G/T]TTTTCCTTTCATGGT	54472
rs566317197	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275817	CAGAAGACCCACTTG[C/T]GGGCATTCTCTTTCT	54472
rs566353449	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275306	GTGGCCACACCTGGG[C/T]GCCTGGACACCGAAG	54472
rs566376578	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299243	GAGCAAGAGAGGAGA[C/T]GGAGACCAGGCTTCA	54472
rs566423168	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289267	AAAGCAGGTAGGGAC[A/G]GGGAGAGAAAAGCCG	54472
rs566471272	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288310	GCAGAGCTTGGAAGG[C/G]CTGTGGGGGTCCTCC	54472
rs566493513	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293031	CTGGCCACGCTGCAG[A/G]GGCTGAGCGGGGGCA	54472
rs566530726	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298607	GGCCTAATGATCAAG[G/T]GTCATTTTTCAACAA	54472
rs566542774	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304264	GTCCACCTGGAGTAC[C/T]GCCCACCTGGAGTTC	54472
rs566569829	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279529	GACGCCATGGGAGCC[C/T]GGGGCAGCCCAGAGC	54472
rs566606562	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1284427	AATCTCGGCTCACTG[C/T]AAGCTCCACCTCCTG	54472
rs566719795	snp	C/T	0.0170251	0.090679	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309248	GCCCCGGCACGGCGG[C/T]GAGCTCAAGCCTCCT	54472
rs566756697	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308263	GCTTGGTGCTGTCCC[A/G]GTGATAGTGAGTTCT	54472
rs566840188	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307445	CGCCGGTGCCCCTCA[A/G/T]AACAGGAAGGGCCTG	54472
rs566855780	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283973	CAACTCAGGACAACC[A/G]GACAGAACTTCACTA	54472
rs566888938	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287787	AGCCTCCCCGCCGCA[C/G]CCTCCCTGCCGCAGC	54472
rs566903834	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1288497	CTCTGTCCTCAGAAC[A/G]TGAGCCCTGCTGTTT	54472
rs566940196	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288060	TGATGCCCCCAGGAG[C/G]TGCAGGTGCCCTGAG	54472
rs566945803	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1293219	ACACGGGGGAGAAGC[C/T]GGGAGGGTGGCCCGA	54472
rs566968888	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304535	AGGCACAGCAGCACC[C/T]GCGCCAGGACGGGGC	54472
rs567096725	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1297376	TCTAAGGCCTGGAGC[A/G]CACAAGCCAGTCAGC	54472
rs567140594	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289572	CACTCTCTGGAAATC[A/C]CACCTGCTGGTGAGC	54472
rs567214763	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274617	CCTGTCTTCTATCTC[C/T]GGAGCCCCGCCTGAG	54472
rs567246050	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279516	TGTGGGCAGAGAGGA[C/T]GCCATGGGAGCCCGG	54472
rs567306419	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293925	AGCTGCACAAGCAAG[A/G]GTCTGAGACACGCCG	54472
rs567379820	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299295	GTTACGCAACCTGCT[A/G]CCCCGCCTACCAGGG	54472
rs567389275	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281449	AGCTTGCACTCTCCA[C/T]AGAGGTGGCAGCTGG	54472
rs567401262	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290191	GCCACGCTCAGCCAC[A/G]TGCAGCCTCCATAAT	54472
rs567575112	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309595	CGGAGACAGTTGTCA[A/C]CTCGAGGCCGCCGCC	54472
rs567589021	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275915	GCAGGTGTCTCAATG[A/G]CATGCAGATTATTTA	54472
rs567629547	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297427	AAACAGAAGGGACCC[A/G]GACGATCCAGGCACC	54472
rs567629608	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302949	TTCCCTCTTCCTATC[A/C]CCCCCTCCCCTCTTC	54472
rs567713421	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284033	CTTTGACCCCACGAC[C/G]GCGGCTCTGGGCTGT	54472
rs567764650	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302449	CTCACTGGTGGCCAC[G/T]GCCATTGCCCTGTAA	54472
rs567836682	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288537	AGTGCCTCCAGGAAA[C/G]AGACAAGGGTGTCTG	54472
rs567867385	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292810	CACAGCGCAGCAGAC[A/G]GCGTTACCACTGCAG	54472
rs567928938	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275154	CCACTGTGTGGGTCC[C/T]TCGGGCCCCCACACG	54472
rs567931731	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1287918	CTCTGCTGCACCCTC[C/T]CTGCTGTCACATCTG	54472
rs567933322	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282762	TTGTGCACATGTACC[C/G]TAAAACTTAAAGTAT	54472
rs567953065	snp	C/T			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311500	TCTTTATTTCTATCC[C/T]GGGAGATTACAAGAT	54472
rs567968249	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1287232	TAAAATCACTGGAGC[A/G]TCATGATGGTTCTGT	54472
rs568049720	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274687	TGCCACGGAGCTGGC[A/G]ATCGGCCTGCATCTT	54472
rs568131009	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299986	GGAGGCCTCTGTCGA[C/T]ACCAACTCTGGAGGA	54472
rs568134734	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307564	CAGGAGGCAGAGGAT[A/G]TCTCCCAGACCACAC	54472
rs568189883	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278758	GGCAATGACGGAAAA[C/T]GAACCGAACCATGGC	54472
rs568245801	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297854	GCTCTGGCTCAGGAG[A/G]GCGCTGAGAGGCCCC	54472
rs568354113	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302889	GAGCACTCATTCGCC[A/G]TGCCTTGTCTCCCCT	54472
rs568516628	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275691	ACAAAAACCACCCCC[A/G]ATCGATGGCAGAAAG	54472
rs568530774	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290940	CCTGCCTGTGCTATC[A/G]GAGTACGTGGGGTTT	54472
rs568530858	in-del	-/GGAGA	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274572	GAGCATCTGCAGAGG[-/GGAGA]GGAGAGGAGGGGGAG	54472
rs568537938	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301620	TCTCAGGGTCAATAT[C/T]ACCCCCACATTGAGA	54472
rs568580930	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1286198	ACGCCAGCCCAGAAT[C/T]GCCCTCCCCATGCCA	54472
rs568620902	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302240	CAAGAGGGCGGGAAC[A/G]CGCACCAGGGCTGAG	54472
rs568652977	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275166	TCCCTCGGGCCCCCA[C/T]ACGGGCTGCTCAAGG	54472
rs568696257	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274835	GTCCTTCTGAGTGTG[A/C]CGACCTCATCCACAC	54472
rs568701008	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1277347	ACAACGCATCCCACC[A/G]GCCTCCCTGAGGAAG	54472
rs568733448	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278770	AAACGAACCGAACCA[C/T]GGCCAGGTGGGGACG	54472
rs568756479	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305959	GGGCCCGCACGGTAC[C/T]CCTCGCAGGGGCCCC	54472
rs568811630	snp	G/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1281929	GCCAGCCTCTCCAAG[G/T]TCTCCGCAGACTTCG	54472
rs568911654	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303010	CAAAGCCAACATGCC[A/G]GGAGGTTCCCTGGCT	54472
rs568947820	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308170	CCCCGCCAAATCTCA[C/T]GCTGAATTATGATCC	54472
rs568948928	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308991	CCGCATCCATCTAGG[A/G]GACCATTAGGGTTCA	54472
rs568971046	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283943	CTCTGTTCTTTCAGG[A/T]TGGCCATTGGCCTCC	54472
rs568971910	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276933	TCCACGGGAGGGGGC[A/G]ACACGGGTGCTCTTT	54472
rs569007730	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1288338	TCCGAGGACACAGGG[A/G]CCTGCAGTGGAGACC	54472
rs569094905	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1283492	GGGGGCTGGGGGCTC[C/T]GGTGGGGCGTCAGGT	54472
rs569194504	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287298	AGACATTTACACATC[A/G]TCACTCACGGCCGGG	54472
rs569253043	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302234	GGCGTGCAAGAGGGC[A/G]GGAACGCGCACCAGG	54472
rs569311084	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1291899	ACGCCAACCCTCGCC[A/G]CACAGCTGAACTCTC	54472
rs569374957	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1296492	GGGGTAAACCATGCT[C/T]CACAGGTGAAAGGTC	54472
rs569439151	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274067	TGGGCTCTCTCAGAA[C/T]GGGGTCGTGTTCCAC	54472
rs569473532	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301717	AGTGAAACTCTGTAC[C/G]CTGAGCCCTAGGTTT	54472
rs569493569	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1285773	TCTGCCAACAATTAG[-/A]AAAAAAAAAAAAAAA	54472
rs569511036	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1307012	ACAGACCCACCGGGC[C/T]GTCACCACACAGCTC	54472
rs569589994	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1295477	CCGGGGTCAATGCCA[A/G]TATCTTTCACACAGA	54472
rs569610069	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278194	GCGTGCGCGGGGCTC[A/G]GCGACCAGTGAGGCA	54472
rs569615226	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295115	CAGTGTGTTTCCTTT[C/T]CCTGCAGTCTTACAG	54472
rs569625665	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300761	GTCCTGGCCTCACGC[C/G]TGCCAGGAGACATCA	54472
rs569646403	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277836	AGCAAAGCTGCAGCC[A/G]ATGCCCAGAATGACA	54472
rs569719219	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281532	TGAGCCCCCGAGACC[C/T]GCACCCTGTGCGGGG	54472
rs569739440	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286450	TGAGTTTGAAAGTGT[A/C/T]AACTTCACATAAGTC	54472
rs569754487	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300365	TCTAAACCACTGCAG[C/T]GTACCTTTCCACACG	54472
rs569777034	snp	A/T	1.71997e-05	0.0029325	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290438	AATGTCAGGAAAAGG[A/T]GGTGCCAACCATCAG	54472
rs569852916	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276943	GGGGCGACACGGGTG[A/C]TCTTTCACGGGAATC	54472
rs569875255	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294645	CGGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA	54472
rs569891582	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280920	CTGAGGCCCAGTGGC[A/G]CCCGCGCTGGTCTCT	54472
rs569964981	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285608	AGCGCAGGGCACGCG[C/T]CACCCAATGGGCGTG	54472
rs569973905	snp	C/T			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309838	AGTCATGACGGTTGT[C/T]GGCGCGGGCCCTAGC	54472
rs570060916	in-del	-/C	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302324	TGCCCAGCTGACTGA[-/C]CCCTCAGTGCGCAGG	54472
rs570067032	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311659	CCATATGCTGATGAT[C/T]CTAAAATCTGTATCT	54472
rs570080722	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305904	AGATCTCACTGCAGA[A/C]GGCAGGGGTCCACAC	54472
rs570184745	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311021	ACCGGCAGCCTGGCC[A/G]CTTGCCTGTTTTGAT	54472
rs570211643	snp	A/C/T	0.000153787	0.00876755	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276637	ATTGTGTGTGCCTTA[A/C/T]ATCAACAGCTCTATT	54472
rs570244567	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1293269	CGGAGTCCGGAGTGC[C/T]CACGGAACACCTGGG	54472
rs570246245	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285938	CCGTTCCCTCCTCCC[A/G]CACCTGCCCTAGGCC	54472
rs570276364	snp	C/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1281733	CGCAGCCAGCACCGC[C/G]TAGCCAGGCAGAGCA	54472
rs570339006	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278702	CCACTGGACACCTCA[A/C]CTCACTGGGGAAGCA	54472
rs570347021	snp	C/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1291491	CTGTCCACACCAACC[C/G]CCCTCTGAGAGTACT	54472
rs570347057	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286836	CACTGCACTGCTGTC[A/G]TCTCTGAGTTTAGTT	54472
rs570384351	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290977	CTGGAACTTGTCTTT[C/T]TTGTGTCTCCCAATC	54472
rs570446266	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1278233	AGGCAGCGTGCGCGG[A/G]GCTCGGCGACCAGCG	54472
rs570485000	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282720	CACCAACATGGCACA[C/T]GGATACATATGTAAC	54472
rs570526988	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287685	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs570575737	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284740	AAAGGCAGCCCTGGC[A/C]CCTGCGCGGGCGGCT	54472
rs570640821	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288847	CTGCAGCCGCACCAT[C/T]GTGGGCCCGCCTCGA	54472
rs570654660	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306704	GGCCCTGCCTTGCGT[A/G]TGCCAGGCAACACTT	54472
rs570680916	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288173	CCCAGGCTTCCCCGA[C/T]ATCTCCAGAGATGCC	54472
rs570728391	snp	C/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1295970	GTCAAGGGTGTCCAG[C/G]CTGGGGCCTGGCCCC	54472
rs570736241	snp	C/T	1.68371e-05	0.00290143	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276988	TTCCTTGGGGAGCGC[C/T]GGGTCGGCGTGTCCA	54472
rs570837729	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300804	GCACCACAGTCGCCC[C/T]TGAAGCACGGCTGGC	54472
rs570864829	snp	C/T	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301091	AGCACTTCATGACTA[C/T]GCGCTGAGCAGCGCT	54472
rs570882420	snp	A/C			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302165	AGTCTGGCCCAGGAG[A/C]AATGGCCCATCCACC	54472
rs570938719	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306242	ATTCTCTCAGAACGA[C/T]GTCGGGCTGGCTAGC	54472
rs571017606	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1280972	AAATTGAGCAGTTGG[C/T]TGCTGTTGCCAGCCT	54472
rs571048771	snp	G/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1281387	TTTCACTGAGGAAAG[G/T]GGACGGTCCTCGTGA	54472
rs571085690	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286304	TCCTCAAATCCAGGA[A/G]GTGACATGGCTCGGG	54472
rs571251562	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291062	AGCTGGGCAGGGACA[C/T]TTGAGGTCCTCGGGG	54472
rs571289887	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276902	AAGAACAGGTGTGGA[C/T]GGGGCGGCACAGAAG	54472
rs571321116	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300166	TCCCACAGAGCTCAC[A/G]GCATTTTATCTTCTC	54472
rs571329791	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1294789	TGTGTCTCCTTTTCC[C/T]GCATTTCTACGAAAG	54472
rs571368891	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293945	GAGACACGCCGCGAG[A/G]AAGGGGTGACGGTGT	54472
rs571431741	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1304942	CTTAGTCTTCTTAGA[C/T]TTGACTTTTTAAAAA	54472
rs571439262	snp	C/G			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298117	TGCAGAAACAGACTC[C/G]TGCTAACCAAGTTCT	54472
rs571543481	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1293401	AGAAGTCACCGGGAT[A/G]TGTGGGCAGAGAGGG	54472
rs571582902	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293000	CGAGAAAGGCCCACG[C/T]GGGAACGGACCTACT	54472
rs571614847	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276516	GAAGCTGCTCAGCTC[A/T]CCAGACCCAAGCCCT	54472
rs571690639	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280090	ATAAACACAACAGCA[C/G]AGAGTTCCATGTGAT	54472
rs571746842	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289281	CGGGGAGAGAAAAGC[C/T]GGGAGGAAAAGGCAG	54472
rs571811563	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1284550	GAGACGGGGTTTCAC[C/T]GTGTTGGCCAGGATG	54472
rs571845638	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1288855	GCACCATCGTGGGCC[C/T]GCCTCGAGTCCCCGT	54472
rs571881988	in-del	-/AGC			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311306	GCAAAGCTACTGAGA[-/AGC]AGCACTAGACAAACC	54472
rs571960619	snp	C/G	0.000284819	0.0119301	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276778	GGCATGAGAAGGAGA[C/G]ACGCACGTCCCAGGG	54472
rs572001716	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280650	ACCCTGGTGCTGCCT[A/C]TGCGGGCCAGGCTGG	54472
rs572030590	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305279	GGAGGCGGTGAGTGC[A/G]TTCCCCGCTGGCTCA	54472
rs572044493	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311223	CCCTTCCTCATTTTC[A/C]CGCTAAAAATCACAC	54472
rs572085828	snp	C/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1291359	CCCAGGAGCTGGTGA[C/T]AGAGACCCCGGGAGC	54472
rs572176578	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285705	CAGAGCTGGGCACAA[A/C/T]GGGGTTTCAAAGCCA	54472
rs572189900	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304569	CGAGGTCTCCGCGTG[A/G]ATCCGGAGGTGGCAC	54472
rs572230566	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304031	ACAGAGCGAGCCTCC[A/C]TGTAAAAAAAAAAAA	54472
rs572254549	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293630	GCTGGGTGAGCTCAC[A/G]TGGAGGAAACAGGCT	54472
rs572260296	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1285673	GTCACCTGACAGGGG[C/T]GTGAGGTTCTCCTGC	54472
rs572267631	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309865	TAGCGTGGCGGCGCT[A/G]CAGTCTGGGCAGTGG	54472
rs572338129	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289393	CAATGCCACAGGTGC[A/G]AGGTGCCAGGACCAC	54472
rs572357492	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284624	AAGGTGCCGGGATTA[C/G]AGGCATGAGCCCCCA	54472
rs572375708	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293594	GGAATGTTTCCCACC[A/G]CTGGAGCTGCGCCAC	54472
rs572394757	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299465	TTCAGTGACGACACT[C/T]GGTCCTTCAGTAAAT	54472
rs572411826	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280329	GTGCCACCGCGTGCA[C/T]GTTCTCTATGGGCCT	54472
rs572432691	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291810	GGGCACGGCCGCCCC[A/G]TCCTCACCGACCCAC	54472
rs572463431	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276229	TCACCCCAGCCTCGC[A/G]AGGCCTGTTGAGAAG	54472
rs572496719	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1284226	ACTTACCCAGATGCC[C/T]ACCCTCCTCTAACTC	54472
rs572498569	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288861	TCGTGGGCCCGCCTC[A/G]AGTCCCCGTCTTATC	54472
rs572525838	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276025	AGATGCTACACGCAG[C/T]GCCCAGGCAGTCAGA	54472
rs572568621	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279686	CACGTTCTTCACGCT[A/G]TGTGAATCTGCTGTC	54472
rs572649311	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1282145	GGGAGAAACAGCTAA[C/T]GCCAGGGCTAAGGCC	54472
rs572654089	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279300	CGGTGTGGGCTGAGG[A/G]GCAGTGGCCTGGCTC	54472
rs572819056	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292754	GGGACACACGGGCAC[C/T]GCTGCTTTCCCCACA	54472
rs572858218	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298248	TCTCCTGGGCACACA[C/T]GGCAGACAGACAGGC	54472
rs572878007	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287750	CCCCGCCGCAGCCTC[C/T]CCGCCGCACCCTCCC	54472
rs573038654	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297640	CCCTGTGAGAGAAGC[C/T]GTACTGCGAGAACAA	54472
rs573118283	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303149	GGACAGAATGAGAAT[A/G]AGCATAGATTATAAA	54472
rs573145835	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303792	TGTAATCCCAAAACT[C/T]TGGGAGGCTGAGGTG	54472
rs573151232	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278885	CGTGGCTTTTTGGGC[A/G]CCCCGGCTGGCAGGC	54472
rs573158874	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302629	GCCTCGGCCTCACGC[C/T]CCACACCAGCCTCCT	54472
rs573193750	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307863	TCAGAAAAAGCAGCT[A/G]TGCCCAAAACCTGGG	54472
rs573290934	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279764	AGGAAAACCAAAACT[C/T]GTCCCTTTTCCATTC	54472
rs573292770	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285227	CTGGGCCTCTGGCCT[C/T]CACCCTCCGTGCAGA	54472
rs573329535	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284718	CGCTCTGCTCTTTCC[C/T]CTGGAGAAAGGCAGC	54472
rs573439114	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296829	GGAGTGGGGTGGAGG[C/T]CTGGTTGCTGGTGGA	54472
rs573488918	snp	C/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1296165	CTAAAGGCAGGGCCA[C/G]TGAACTGCAGGTCAC	54472
rs573507013	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1287016	GAAACTGTCAGCTGC[A/G]GATAAGTCACTGCAC	54472
rs573618573	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288927	TCGATGAGACCCCTC[A/G]GGCAGCGCAGGCTTC	54472
rs573654819	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293059	GCAGTGGGTGGGTGC[A/G]GGGGGCTCCAGGCCT	54472
rs573932447	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298764	CCGCAGCCAGCGCCA[C/T]GTGGCGGGGCAGGTG	54472
rs573967356	in-del	-/AG	0.00159617	0.0282053	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273871	CGGGGGTTGGGCAGC[-/AG]AGAGGGGGCAGACAC	54472
rs573996938	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275000	AAATGAAGGAAAGAA[G/T]AATCTTATTTAATTA	54472
rs573998177	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303219	CCAGGAACTCCACTG[C/G]AGGCAGCCTTGCATC	54472
rs574050852	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1307647	GGACACAACAGCAGG[A/G]TGCTGGTTCCCTTGT	54472
rs574070465	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307965	GGATACAGTGTTAAG[A/G]GTGGGGAGCCCTGGT	54472
rs574095821	snp	A/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279256	ACTTGGGGAGCAGGC[A/C]CCCCCGGGGGAAGAG	54472
rs574143830	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297069	CCAGCCGTCTGCAGG[A/G]GCCCCGGTCAGCGCC	54472
rs574179624	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288106	GAGCCAGGGCGCTGA[C/T]GTGCTGGCCCCACAG	54472
rs574182993	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301833	AAGGGACAGAGGAAG[C/T]TAATGAAACAGAGAG	54472
rs574237347	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1287412	CTCCCCGCCGCAGCC[C/T]CCCCGCCGCACCCTC	54472
rs574311497	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283215	CCCTGCCAGCAGCCC[C/T]GGGGAAACTCAGCCC	54472
rs574347097	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282141	TCCTGGGAGAAACAG[A/C]TAACGCCAGGGCTAA	54472
rs574416011	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291292	TGCCTGGAATGCAGA[C/T]GGCCTCCCTGTACCA	54472
rs574435713	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296276	TTCCACATGAAACAG[A/C]TGAAATTCAAAAGTA	54472
rs574450817	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299387	ACGAGGAGGGAGTGC[C/T]ACCAGTTCATGCTTC	54472
rs574489275	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300883	GGCCCCCTGCGGAGC[C/T]TTTTTAAACCTTCTC	54472
rs574519293	snp	C/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1286579	TCACTGCACCGCTGT[C/T]GTCTCTGAGTTTAGT	54472
rs574582790	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296126	CACCATGTGTGCCCA[C/T]GGCTTCTTTCTCCTT	54472
rs574593234	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1277996	CCCACAGCTACGCAG[A/G]CCCCTCGCCCCATGT	54472
rs574621415	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1282997	ATTGCTGGGGAAGTC[A/G]GATAAACTCAGGGGC	54472
rs574699846	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1295948	TTCCTCATCTCTAAA[A/C]GGAGGGGTCAAGGGT	54472
rs574776550	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287587	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs574838985	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290171	GCAGGTGTGTCCCCA[C/T]GGCAGCCACGCTCAG	54472
rs574942163	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292217	CTTACACTCCAAACT[C/G]TGCCCCTGTAAACTC	54472
rs574971772	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297602	CCCCGTTTTTGACTG[C/G]GACACGTCACGAGTG	54472
rs574983645	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288335	TCCTCCGAGGACACA[A/G]GGGCCTGCAGTGGAG	54472
rs575118508	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274328	GATTCGTTACTCCTG[C/T]GTATTGTGAATTAAG	54472
rs575133767	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300825	CACGGCTGGCCACAC[A/G]CAGGCGGCAGGAGAC	54472
rs575155708	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278359	CTAGGATCACTGGAG[C/T]GCTAGAGCCCCAATC	54472
rs575170466	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300569	AATATTCCTGTTGGT[A/G]ACACGTCTCCAACGG	54472
rs575231376	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278047	GAGATGCAATCTATC[A/G]AGCAGGAGACGCACG	54472
rs575235677	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1305638	CCCTCTGCCATCCCT[A/G]ATGAAGTCACCGATT	54472
rs575261081	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302588	TGGACCAGTACCTGA[C/G]CCTGCAGCCCCTGGC	54472
rs575350597	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301916	CAAAGCCTCTTGGGC[A/G]AGGTCTGAGTGTCTG	54472
rs575408206	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279326	GGCTCACTCCCCTCC[C/T]TCCTGCAGGGCAGAG	54472
rs575445589	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283600	AAATTTACAATGTCT[A/G]TCAAAAGAAAATTTC	54472
rs575481291	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306786	GTGCCCAGGACCCTC[C/T]GGCGGCCTCCAGCTC	54472
rs575547280	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1282938	ACTTAAAATATAATT[A/T]AAATAAATAAATAAA	54472
rs575796355	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307263	GCGTTTACCGGTCAA[C/T]GGGGGTGCCCCTGAA	54472
rs575819559	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291235	GCCCTCGTAAGCTGG[A/G/T]TTGGGTTCAGCCCTG	54472
rs575841958	snp	C/G	0.000186272	0.0096489	intron-variant	TOLLIP	GRCh38.p7	11:1283582	AAGTGCGGGGCTGTT[C/G]CAAAATTTACAATGT	54472
rs576060320	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300588	CGTCTCCAACGGAGA[C/G]AGCCGCTGCTTCCTT	54472
rs576066936	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1294062	ATTTCTATGAAAGCC[A/G]CGTGGCTCACAGTGT	54472
rs576114567	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293704	CAGAGGCGTGGGCAA[C/T]GCCAGGGCCACCTCC	54472
rs576121845	snp	A/G	0.00358779	0.0422022	intron-variant	TOLLIP	GRCh38.p7	11:1277449	CCCAGGCACAGCCAC[A/G]GGGAAGGTGGGCAGG	54472
rs576222040	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286150	CCACCCATCAGAACC[C/T]CGGGAATCGCCCTCC	54472
rs576261203	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290012	GCTTGTCACTGGGGA[A/T]GTTTCCAAATGTAAG	54472
rs576269041	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289750	CTGTGCGCCCAGCGG[A/G]GCGGACACATGCATG	54472
rs576280891	snp	C/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1280289	AACTCACAGGCGCTG[C/T]GAACGCCGGCTGCTC	54472
rs576440293	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293348	GTGGTCGGCTCAGGC[A/T]GGGGCCAGCACATGG	54472
rs576495566	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305146	CGTGGGTCCCCACAC[A/C]GTGAAAAGATGTGAT	54472
rs576511076	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304692	TAAGTGCATGTTACC[A/T]TTTCCAGGGGAGCCC	54472
rs576514565	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306498	GGAAAGCTGAGCGAG[C/T]GCCCTGCTTAACCTC	54472
rs576578561	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276303	GCAGGAGAGACGGAC[A/G]GCAGCCTCCGGCGGG	54472
rs576734578	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290500	CCTGAACCCTTCCAC[A/G]AGGCCTTTTCCTAAC	54472
rs576773317	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287736	CTCTGCCGCAGCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs576817740	snp	A/C	0.00398564	0.0444627	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301363	AGTCTCACACCAGCA[A/C]TGAGGATCCCACACA	54472
rs576834547	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279947	AGAGCAGGTGGGGAC[A/G]ACCGTCCAGCTCAGA	54472
rs576846336	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300937	CGAGGCTGTGGAGGT[A/G]CTGTTTGTGTCTGTG	54472
rs576856208	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301449	GATCGCACATGTGTC[A/G]CGGGCTTCCGAGAAC	54472
rs576871798	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290122	CCAGGTGGGGAGCCA[C/T]GCCTCGAAGCCAGCC	54472
rs576943773	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1294135	AGTGTGTCTCCTTTC[C/T]CTGCATTTCTACAAA	54472
rs577000072	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1281587	GACAGCTGAATGAAC[A/G]AGCGGCTGAAGGGGC	54472
rs577070169	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286173	CGCCCTCCCCACAAT[C/T]GCCCTCCCCACGCCA	54472
rs577217625	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276316	ACGGCAGCCTCCGGC[A/G]GGCGAAGGACCCGGC	54472
rs577321334	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300098	TTTTTAGAAACTTTT[C/T]AAAAACATTCGTGAA	54472
rs577459283	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305231	AAATCCAGCGCAAAG[C/G]TTCACAGGAACCCAG	54472
rs577565877	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280592	TGGAAACAGCGTCAA[C/T]GGGCAGCTGCAGCCA	54472
rs577598023	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280325	CATGGTGCCACCGCG[C/T]GCACGTTCTCTATGG	54472
rs577670776	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310602	TACATATAAACAAGC[C/G]TACCCAGGTGGACGC	54472
rs577707023	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309753	CTCGCCCGGCGCCTG[C/T]GCACCTGCTCTCTCC	54472
rs577848907	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299436	AGTCCAGGTGCTGAA[A/G]TAAACCCTATCGTTT	54472
rs577913129	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303833	TTGAGACCAGGAGTT[C/T]GAGAACAGCCTGGCC	54472
rs577924092	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298410	GGGTGGTCACAGGGA[C/T]GTGTGGGCGTGGGGT	54472
rs577926654	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292736	CAGACAGCAGACACC[A/G]TGGGGACACACGGGC	54472
rs577957541	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288969	TCAGCCTCCGTAGGG[A/G]ACTTCTTCCCTCTCT	54472
rs577986037	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293198	GTGTGGGGCAGCCAC[C/G]TGCGGACACGGGGGA	54472
rs578112558	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275479	AAGACCAGGCCATCT[A/G]AGACAGGGAATCCCA	54472
rs578115666	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279613	ATCTGCCGCGCTCAG[C/T]CCCACCAGCCACCTG	54472
rs578133277	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289433	CAGCCTCGCCACATC[C/T]CCTCTGACCTTCTGA	54472
rs578168030	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1288569	GGGGCGGCATAGCCC[C/T]GACGTGCTCCAACAT	54472
rs578176877	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283789	GTTGATGGAACTGCA[C/T]CCCCCAAAAAGACAG	54472
rs578216369	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1279264	AGCAGGCACCCCCGG[A/G]GGAAGAGGTGGGTGC	54472
rs745316051	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1297634	CCTTTGCCCTGTGAG[A/C]GAAGCCGTACTGCGA	54472
rs745333203	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1294244	GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG	54472
rs745355871	snp	A/G	0.000187494	0.00968049	intron-variant	TOLLIP	GRCh38.p7	11:1283501	GGGCTCCGGTGGGGC[A/G]TCAGGTGGACGAGTC	54472
rs745365179	snp	C/T			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274285	TTCCTGCTCCCAGTC[C/T]GTTGACGAGTGAACT	54472
rs745408327	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282321	ATTCATAAGGGATTC[C/T]GACCCAAGGAAAAAA	54472
rs745479963	snp	C/T	3.53369e-05	0.00420324	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295672	GATGTTCAGTCGGCC[C/T]ACGGTGCCCACTGCG	54472
rs745564863	snp	A/G	4.88424e-05	0.00494154	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295737	CCAGCTGGACCTGCC[A/G]CTGCTGCTGTGTGGG	54472
rs745642953	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279012	CACGTCTCCCCACAG[C/T]GTGGCAACATGAGGA	54472
rs745828096	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298538	CACTCTTTAGGTGTC[C/G]GTTAAAGACAGTGGG	54472
rs745831903	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287274	AGCGTCTGTTAAAGA[C/T]GTGTCATGAGACATT	54472
rs745863976	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1293305	CATGTGGCCATGGTC[C/T]GTACCTAGGGATCTG	54472
rs745892746	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1284318	TCTTTCCTCGGTGAC[A/G]GGGTGCAGGTGCTAC	54472
rs745957373	snp	A/G	0.000115895	0.00761144	missense, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309491	TGAGTGCTGACGGTG[A/G]TCGCCATGGTGCTGC	54472
rs746015012	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292712	CCACAACGGGCAAGA[A/G]ACGCACGTCAGACAG	54472
rs746054511	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304593	GTGGCACAGACAATG[A/T]TTAACTTCTTCTTTA	54472
rs746105178	snp	A/G	3.32784e-05	0.00407898	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277032	AAACGGCATCGAGGC[A/G]GAGGCTCTATGGCTC	54472
rs746113571	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279511	CAAAATGTGGGCAGA[A/G]AGGACGCCATGGGAG	54472
rs746207071	snp	C/T	1.66735e-05	0.00288729	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288694	CTCAGGCTGTACCAC[C/T]TGTCCTCCACCTTGC	54472
rs746335376	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310227	CGCTCCTCTCCTGCT[C/G]GCTCCGGAGAACCCC	54472
rs746384403	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1285198	CCTGCCCGCAACTTG[C/G]CCACTTCCATGGCCT	54472
rs746435542	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288476	AAACCACCCAGGGCC[C/T]CTGCCCTCTGTCCTC	54472
rs746448684	snp	A/G	8.68832e-05	0.00659045	intron-variant	TOLLIP	GRCh38.p7	11:1288615	ACCCCGCCCAGGCGT[A/G]CAGCTCACCGCGTAG	54472
rs746543908	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275159	GTGTGGGTCCCTCGG[A/G]CCCCCACACGGGCTG	54472
rs746556447	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298756	CCCGGGGACCGCAGC[C/T]AGCGCCATGTGGCGG	54472
rs746633236	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308057	AAAGGACTTTTTCCA[C/T]CCACGGCATGTTCAG	54472
rs746707461	snp	C/T	3.4845e-05	0.00417388	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290451	GGAGGTGCCAACCAT[C/T]AGGAGAGGGTGGGTT	54472
rs746801284	in-del	ACCTCTGAGGGCACGGCCGCCCCGTCCTCACCGACCCA/C			intron-variant	TOLLIP	GRCh38.p7	11:1291787	CGTCCTCACCGACCC[lengthTooLong]CCTCTGAGGGCACGG	54472
rs746886563	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304727	ACTTTCCCAGCACAG[A/T]GTGTATGTACTTGAG	54472
rs746904361	snp	A/G	3.53033e-05	0.00420124	missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277226	AGGGCCACGGGCACC[A/G]TGCCGGGGCTACAGA	54472
rs746987940	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274510	ATAATCAGAAGCGCA[C/T]GTTCTGAGACCACTC	54472
rs747030195	snp	C/G	0.000141453	0.00840871	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276868	TGGACCGCCAGGAAC[C/G]GAAAACCCACATGCA	54472
rs747137810	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285295	CGAGAGAGGCCACCT[C/T]AGCAGGAGAACCAGG	54472
rs747147065	in-del	-/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302790	CTCCCACGCCAGTGT[-/G]GGACGGGCAGTGGTG	54472
rs747168250	snp	A/G	1.79745e-05	0.00299782	intron-variant	TOLLIP	GRCh38.p7	11:1288813	GGCCCCAGGCATCAG[A/G]GAAGGGGCCACCCTG	54472
rs747260630	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293563	GGGCTGAGCTACCTG[A/G]CCCAGTGAGGAGGCA	54472
rs747375576	snp	A/G	3.98764e-05	0.00446504	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286092	TGGCAGCTGGAAGCA[A/G]CTGAAACACAGCGGA	54472
rs747426885	snp	C/T	3.49327e-05	0.00417913	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295760	TGTGTGGGCGTGATG[C/T]GGAGGAAGTCCTGCG	54472
rs747435406	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301687	CCACGGAGGCCCCAA[C/T]ACAGAAGCCCAACTA	54472
rs747453098	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302897	ATTCGCCGTGCCTTG[A/T]CTCCCCTTCCGGGGC	54472
rs747545736	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279631	CACCAGCCACCTGCA[C/T]GCACGCGGACGGATG	54472
rs747591575	snp	C/G	5.14681e-05	0.00507261	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309428	CGCCCGCAACCGCAG[C/G]TCACCGCCCCCGCCC	54472
rs747674247	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288948	CGCAGGCTTCACGAT[C/T]GTATATCAGCCTCCG	54472
rs747682221	snp	G/T	5.00805e-05	0.00500378	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290345	GTCTCGTACACCGCG[G/T]AGCCCAGGCGCAGTC	54472
rs747714909	snp	C/T	0.000122334	0.00781997	intron-variant	TOLLIP	GRCh38.p7	11:1288612	CCCACCCCGCCCAGG[C/T]GTGCAGCTCACCGCG	54472
rs747815447	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276020	GGCCAAGATGCTACA[C/T]GCAGCGCCCAGGCAG	54472
rs747839576	snp	C/G	1.91349e-05	0.00309307	intron-variant	TOLLIP	GRCh38.p7	11:1295834	CCAGTGAGTCAGGGT[C/G]GGGGCACAAAGCAGC	54472
rs747843055	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280675	GGCTGGGGAGGCGCC[A/G]GACGCCCCACTTTCC	54472
rs747921776	snp	C/T	6.99839e-05	0.00591499	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277218	CCGGGGGCAGGGCCA[C/T]GGGCACCATGCCGGG	54472
rs748072745	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1293050	TGAGCGGGGGCAGTG[G/T]GTGGGTGCGGGGGGC	54472
rs748102705	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291171	GATGGCAGGTTCAAA[C/T]ATAAAACCTAAAACT	54472
rs748152746	snp	A/C	1.75047e-05	0.00295839	intron-variant	TOLLIP	GRCh38.p7	11:1288800	GACAAGAGGGAGAGG[A/C]CCCAGGCATCAGGGA	54472
rs748152949	snp	A/G	1.65638e-05	0.00287778	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277156	GAACATGTCCTGGAT[A/G]GCTTTCAGGTCCTCC	54472
rs748173658	in-del	-/AG			intron-variant	TOLLIP	GRCh38.p7	11:1283677	GAAAGGCATCTACAA[-/AG]AGAATTAGGGATAGG	54472
rs748195691	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288821	GCATCAGGGAAGGGG[C/T]CACCCTGCCCCTGCA	54472
rs748203339	in-del	-/CT			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299758	TCAGGAGCCAGTCCC[-/CT]GTCAATGCTCACTCG	54472
rs748223536	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1277773	TGGCAAGTGTGTCAC[C/T]AAACTGTGTGCCGGT	54472
rs748276802	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287148	GCTGTCTTCTGAGTT[C/T]GAAACTGTCAACTGC	54472
rs748279004	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276908	AGGTGTGGACGGGGC[A/G]GCACAGAAGTCCACG	54472
rs748356234	snp	A/T			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310028	ATCCCCTGCAGGGCG[A/T]TCTTTCCCTCAGCTG	54472
rs748403718	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1286298	ACCACCTCCTCAAAT[A/C]CAGGAGGTGACATGG	54472
rs748439890	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1288206	GCCACACCACGGCCA[A/T]TGCCTGCCCTGTGGG	54472
rs748466457	snp	A/G	3.33389e-05	0.00408269	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288729	CCTCAGGGACTCCGG[A/G]ATGGTGATGTGGGTC	54472
rs748528354	snp	A/G	8.79752e-05	0.00663173	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295750	CCGCTGCTGCTGTGT[A/G]GGCGTGATGCGGAGG	54472
rs748563320	snp	A/C	0.000142501	0.0084398	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276725	CCAACACCCTGGCAG[A/C]AGCAGCTGCTCTCTA	54472
rs748637327	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290782	CAGAGCTGAGAGCCA[C/G]AGCATGACATGGAGT	54472
rs748791889	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281440	TCAGTCTCCAGCTTG[C/T]ACTCTCCATAGAGGT	54472
rs748842880	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290436	CCAATGTCAGGAAAA[A/G]GAGGTGCCAACCATC	54472
rs748844883	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280583	GGGAACAGATGGAAA[C/T]AGCGTCAACGGGCAG	54472
rs748967805	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289756	GCCCAGCGGGGCGGA[C/T]ACATGCATGCTCTGT	54472
rs748972033	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1287226	TGCAGGTAAAATCAC[A/T]GGAGCGTCATGATGG	54472
rs748987248	snp	G/T	0.00163332	0.0285305	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309636	GCTGACAGCCGCCGC[G/T]CCCCGCCCCCGGCAC	54472
rs748996297	snp	A/G	0.000106125	0.00728363	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286057	TGGCATCAGGACCAC[A/G]GGCTGGGGTGGCATC	54472
rs749010912	snp	C/T	3.31879e-05	0.00407343	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277042	GAGGCAGAGGCTCTA[C/T]GGCTCCTCCCCCATC	54472
rs749051977	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291053	CAGGTGCTCAGCTGG[G/T]CAGGGACATTTGAGG	54472
rs749138695	snp	C/T			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274202	CTGTTGAGGGAGGAG[C/T]ACCTGGGACTTCCCT	54472
rs749188185	snp	A/G	1.68539e-05	0.00290287	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290260	ATAGAAAGAGTCCAC[A/G]CCTGGGGGCACCGTG	54472
rs749210546	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295907	CCCATGTCCTTATCA[A/G]GTCCTGGACTGTGCT	54472
rs749210547	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1307257	TACTATGCGTTTACC[A/G]GTCAACGGGGGTGCC	54472
rs749248053	snp	A/G	0.00011687	0.00764339	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290342	GGCGTCTCGTACACC[A/G]CGTAGCCCAGGCGCA	54472
rs749337956	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309946	GGCGGGGGTGACCTT[C/G]GGACGTGCGACCCGC	54472
rs749455035	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303115	TGTAAGCTGAAGAGC[A/G]GTGAAAGGGAAGAGT	54472
rs749635021	snp	A/G	0.000713012	0.0188679	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276712	CGCTCCACCACCTCC[A/G]ACACCCTGGCAGAAG	54472
rs749721078	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1283885	GAGTGGCCCTGCCTA[C/T]GGGGCTTCGACTTCC	54472
rs749743149	snp	C/T	1.66668e-05	0.00288672	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288704	ACCACTTGTCCTCCA[C/T]CTTGCCCTGCCTCAG	54472
rs749808523	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1288091	AATGGAGATGGCTGG[C/G]AGCCAGGGCGCTGAC	54472
rs749858766	in-del	-/AG	0.000142197	0.00843079	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276746	CTGCTCTCTACAGCA[-/AG]AGCATTTTCCAGAAC	54472
rs749898213	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1293054	CGGGGGCAGTGGGTG[C/G]GTGCGGGGGGCTCCA	54472
rs749948104	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1283463	CTGCTTATTGGAAAC[C/G]CATGCCTGGGCATGG	54472
rs750262958	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279818	CCTGATCTCAGACCA[C/T]GCAGCATGGTAAGTC	54472
rs750343352	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1284596	CCTCACGATCTGCCC[A/G]CCTTGGCCTCCCAAG	54472
rs750357564	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309657	CCCCCGGCACCGCCC[C/G]ACTGCGCAGGCGCCG	54472
rs750385575	snp	C/T	1.79081e-05	0.00299228	intron-variant	TOLLIP	GRCh38.p7	11:1288589	TGCTCCAACATACCC[C/T]AATGCGCCCCACCCC	54472
rs750436133	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1277879	CATACAAACTACACC[-/A]AGAAAATGCTCACAA	54472
rs750467931	snp	A/C	1.65269e-05	0.00287457	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277122	GCACGGAGCGGATCA[A/C]CTCCTGGTCCATGTT	54472
rs750520175	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280926	CCCAGTGGCACCCGC[A/G]CTGGTCTCTCACGCA	54472
rs750543906	in-del	-/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299224	TTTAACCTGAAGACA[-/G]GAAGAGCAAGAGAGG	54472
rs750573151	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290127	TGGGGAGCCACGCCT[C/T]GAAGCCAGCCAGGAA	54472
rs750630501	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280142	AGCATCCAATTCTCA[C/T]TTTGAATGGAACCAT	54472
rs750664805	snp	A/C	1.67944e-05	0.00289775	missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290400	TGCCGTAATTCTTGG[A/C]CAACTTTGCCTGGAA	54472
rs750685650	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289464	CTCTGCCTCAGAAGC[A/G]CTGCAGGTGCAGCCA	54472
rs750775456	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301988	ACATAGAACAGCACA[A/G]TTGGTCCAGATGAAG	54472
rs750825110	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1296206	GAATGAGACAAAAGC[C/T]GAGCCTCAGGTCTAA	54472
rs750836999	snp	C/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311391	CCCCCTGGCGGCGGG[C/G]CCCCCCACCGTTTTC	54472
rs750868280	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275381	TGGGTTAGAGTTGTT[A/G]ATATCACGGAACATA	54472
rs750949656	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306902	GCCCAACCCCTACTC[C/T]CATTCCTCCTCCGAG	54472
rs751009667	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308580	CTCTGAGTCAGTCTA[C/T]ACCAGCTCTCCTGCA	54472
rs751025957	snp	A/G	0.000147308	0.00858092	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276824	GAGACCTCCCAGCAC[A/G]AGATGGGAGGGGAGC	54472
rs751122359	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284745	CAGCCCTGGCACCTG[C/T]GCGGGCGGCTTCACA	54472
rs751211641	snp	A/G	1.68658e-05	0.0029039	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288765	AATGCGGTCGTCCAT[A/G]GAGAAGGCTCTCTGC	54472
rs751224628	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308314	GTGTGTGGCACCTCC[C/G]CACCCCCAACTCTCT	54472
rs751227418	in-del	-/CGCCGGGCGACCTCCTGCGCCCC	0.000110748	0.00744055	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309541	GACCCGACAGTGACG[-/CGCCGGGCGACCTCCTGCGCCCC]CGCCGGGCGACCTCC	54472
rs751232717	snp	C/T	0.000299895	0.0122416	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276648	CTTAAATCAACAGCT[C/T]TATTCCAATTACATC	54472
rs751283160	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293157	GAGCACCAGCAGCAC[A/G]AGGGCTTTGGGCCTC	54472
rs751360385	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289510	ACCCTCAAGGGTCAC[A/G]ACCATTCGCACCACC	54472
rs751365751	snp	A/G	0.000101999	0.00714067	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290242	CTCATCGAAGATCTC[A/G]AGATAGAAAGAGTCC	54472
rs751369813	snp	A/G	0.000132319	0.00813277	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286009	ACACGCACCTGTGAT[A/G]GGCACATAGCCAACG	54472
rs751384463	snp	A/C	2.32393e-05	0.00340868	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295731	GGGCGTCCAGCTGGA[A/C]CTGCCGCTGCTGCTG	54472
rs751426226	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301541	AAATCCAGGAGCTGT[C/G]CTGGGGAGGCACACA	54472
rs751456325	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276181	GCCACCACACCCTCT[C/T]GGAATCATGCACAGT	54472
rs751526929	snp	A/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311554	TGACTCCTTAACATC[A/G]GAGTGCCTTACCTCA	54472
rs751558926	snp	A/C	4.70024e-05	0.00484758	intron-variant	TOLLIP	GRCh38.p7	11:1277304	AAAGTTCCAGAAGTG[A/C]CACACTAGCTCCTGC	54472
rs751591973	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299687	TGTACAAGATGCACA[C/T]ACTGAGTTCAACACT	54472
rs751648815	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1307020	ACCGGGCCGTCACCA[C/T]ACAGCTCAGCTGTCC	54472
rs751662283	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292336	TCTCTGCCTAGCTGC[C/T]ATGACTTATTTTTAT	54472
rs751669567	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273929	AACGCGTCCGTGCCC[A/G]GGTGCCAGGGTGGCT	54472
rs751847765	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1281040	GAGAACATGCTTCAT[C/G]AGGCCACGCGGTCTC	54472
rs752015473	snp	A/G	1.65228e-05	0.00287422	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277111	CTGGGCTTCCAGCAC[A/G]GAGCGGATCACCTCC	54472
rs752083742	snp	A/G			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297944	AGGCCAGGGCCCTTC[A/G]CCTGCCTCCCAGAAG	54472
rs752085961	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287031	GGATAAGTCACTGCA[C/T]CACTGTCGCCTCTGA	54472
rs752140732	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301408	GCGCCTGCCCACCCT[C/T]CCCACCCACCTCACA	54472
rs752238933	in-del	-/GCCGCAGCCTCCCCGCCGCAGCCTCCCC			intron-variant	TOLLIP	GRCh38.p7	11:1287795	CGCCGCACCCTCCCT[-/GCCGCAGCCTCCCCGCCGCAGCCTCCCC]GCCGCACCCTCCCCG	54472
rs752257387	snp	C/G	0.000156262	0.0088378	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276629	TGTGAGGGATTGTGT[C/G]TGCCTTAAATCAACA	54472
rs752258393	snp	C/T			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310863	TTCTCAGTCCTCGTC[C/T]TCCGGGAACTACAGC	54472
rs752357982	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1286915	CAAAACTGTCCACTG[C/T]GGATAAGTCACTGCA	54472
rs752410068	snp	A/C	1.67038e-05	0.00288992	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288666	GCCCTCCTTGTCGTC[A/C]CCCTGCCTCCCGCTC	54472
rs752477013	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281129	ACATGATGCCTACCA[C/T]GAATTATTTGAAATC	54472
rs752481801	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1307140	GCCACAGTTGGTAGC[A/G]CTGGTTGATTAAGTC	54472
rs752522549	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281967	GCTGGCAGTGGCTGC[C/T]GGGAGGATGGGCTGT	54472
rs752535779	snp	C/G	3.84741e-05	0.00438584	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295716	GCTGCTGGGCCGCCT[C/G]GGCGTCCAGCTGGAC	54472
rs752566191	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1285412	GGCCGGTCTTGCACC[A/T]GCAGCTACCACAGTC	54472
rs752568534	in-del	-/C	1.73993e-05	0.00294947	intron-variant	TOLLIP	GRCh38.p7	11:1295798	ACCGATGTACACCTG[-/C]GGGGCCGGGGACCAG	54472
rs752656167	snp	A/G	3.3592e-05	0.00409815	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290273	ACGCCTGGGGGCACC[A/G]TGCAGTGGATGACCT	54472
rs752716243	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288309	GGCAGAGCTTGGAAG[A/G]GCTGTGGGGGTCCTC	54472
rs752730324	snp	A/G	1.80866e-05	0.00300715	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295649	CCAAGGCCCACCTGT[A/G]CCACCGTGATGTTCA	54472
rs752812201	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274908	GCTAATTCTGGGGAC[C/T]GCTCGGAGGGGCTCA	54472
rs752968195	snp	C/T			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273996	TTTGCTCCCTAAGCA[C/T]GAGCCAGTCATCACT	54472
rs752973555	snp	A/G	6.03336e-05	0.0054921	intron-variant	TOLLIP	GRCh38.p7	11:1285977	TCTACCAGGGGAGAG[A/G]CACCCAGGGAGGGAG	54472
rs753002093	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307782	CAGAGGCCGTCCAGG[A/G]CCTCTGCCGACCCGT	54472
rs753157997	snp	C/T	1.67094e-05	0.0028904	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290315	GGATTCTTGGCGCCA[C/T]TGTGTGCCGTGGGCG	54472
rs753163109	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279334	CCCCTCCTTCCTGCA[A/G]GGCAGAGGCCATGTG	54472
rs753207564	snp	A/G	1.77896e-05	0.00298237	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290216	CATAATAGCTGGCAC[A/G]TCCCTCTCACCTCAT	54472
rs753216242	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1278890	CTTTTTGGGCGCCCC[A/G]GCTGGCAGGCGGGCA	54472
rs753314727	snp	C/T	1.77719e-05	0.00298088	intron-variant	TOLLIP	GRCh38.p7	11:1288598	ATACCCCAATGCGCC[C/T]CACCCCGCCCAGGCG	54472
rs753434222	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302692	GGCCTCATGCTCCAC[A/G]CCAGTCTCCTGGCAC	54472
rs753477389	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1278390	TTAGGATAGGACTTT[C/T]GTTCCTTTCTACACT	54472
rs753616897	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308667	GAAAGGTTCTCTGAA[A/G]TTCCTGGCGCCTATC	54472
rs753616952	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298465	TGGGTCCCTCGCTGC[C/T]CTGGATCCTGGTTGT	54472
rs753643659	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274979	TCAAACAGGAAATAA[A/G]GCATAAAATGAAGGA	54472
rs753643804	snp	A/G	1.70758e-05	0.00292192	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290426	TGGAATGAAGCCAAT[A/G]TCAGGAAAAGGAGGT	54472
rs753725179	snp	A/G	1.67548e-05	0.00289432	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288649	ATGACGAGGTTGATC[A/G]TGCCCTCCTTGTCGT	54472
rs753786197	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1292219	TACACTCCAAACTCT[G/T]CCCCTGTAAACTCCT	54472
rs753786267	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1282114	CAGTGTTCTCCTAAT[A/G]GGAACCAGGGCTCCT	54472
rs753798329	in-del	-/AGAA	1.69484e-05	0.002911	frameshift-variant, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290247	CGAAGATCTCGAGAT[-/AGAA]AGAGTCCACGCCTGG	54472
rs753866833	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282274	GGGGCTCCCTCTGGC[C/T]AAATCTGGAATAATT	54472
rs753947060	snp	A/C	2.08901e-05	0.00323181	intron-variant	TOLLIP	GRCh38.p7	11:1277282	TCAAGTTTGGTAAAA[A/C]CGTCGGAAAGTTCCA	54472
rs753965639	snp	C/G	0.000110867	0.00744454	intron-variant	TOLLIP	GRCh38.p7	11:1295616	AGCGCACCAGCCCCA[C/G]GCAGGCAGGAGGGTG	54472
rs754062309	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275593	CACAGCTGAAGAAGG[C/T]GCCTGCTGCCAGCAT	54472
rs754136374	snp	C/T	3.4647e-05	0.00416201	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295692	TGCCCACTGCGCCTC[C/T]GTACTGCAGCTGCTG	54472
rs754146163	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295513	TTCAACATCACACAG[A/G]TTTCAGGAAAAGCGG	54472
rs754280676	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293247	CGAGAGCTCCACCTT[A/G]GGCACACGGAGTCCG	54472
rs754283499	snp	G/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290023	GGGATGTTTCCAAAT[G/T]TAAGTATGTTCAAGG	54472
rs754370533	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279963	ACCGTCCAGCTCAGA[A/G]ACTGTTCCGGAACTC	54472
rs754515386	snp	C/T	1.67494e-05	0.00289386	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288650	TGACGAGGTTGATCA[C/T]GCCCTCCTTGTCGTC	54472
rs754558708	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309950	GGGGTGACCTTCGGA[C/G]GTGCGACCCGCTCGG	54472
rs754655632	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284940	TCTAGGGCGAGGTCC[C/T]GACTCCCAAGGTGGC	54472
rs754656564	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302513	AACTGCAATTCCCCA[C/T]GCCCACTCAGCTGCT	54472
rs754681451	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281048	GCTTCATGAGGCCAC[A/G]CGGTCTCCAGATGCT	54472
rs754769806	snp	A/G	3.42695e-05	0.00413927	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290431	TGAAGCCAATGTCAG[A/G]AAAAGGAGGTGCCAA	54472
rs754824984	snp	A/T	3.65344e-05	0.00427386	intron-variant	TOLLIP	GRCh38.p7	11:1295636	GCAGGAGGGTGCCCC[A/T]AGGCCCACCTGTACC	54472
rs754899704	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301382	GGATCCCACACAAAC[A/G]GCATCCGCAGGCGCC	54472
rs754949925	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300659	CCGACTGAGAGTGCC[A/G]CTGCTTCCTTGGGCC	54472
rs755015129	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287038	TCACTGCACCACTGT[C/T]GCCTCTGAGTTCAAA	54472
rs755167572	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273979	CTCACATTTATGGGC[A/G]CTTTGCTCCCTAAGC	54472
rs755200585	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275857	CAGTGGGTTTACATC[C/T]GAAGGCCGGCGGCAA	54472
rs755204095	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306221	TGAAGATCTAAACAC[A/G]GTATGATTCTCTCAG	54472
rs755225179	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1307051	TTATGTGCTGCCATG[A/T]CTACCGTGCTGCCCT	54472
rs755327679	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291870	CGACCCCCGAGGGCA[C/T]GGCTGTCCCGTCCAC	54472
rs755406670	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302883	CTCGCTGAGCACTCA[C/T]TCGCCGTGCCTTGTC	54472
rs755412103	in-del	-/AAC			intron-variant	TOLLIP	GRCh38.p7	11:1296325	AGTAAATCGATTCCA[-/AAC]AACCACGAAAGACCT	54472
rs755432979	snp	A/G	3.43601e-05	0.00414474	intron-variant	TOLLIP	GRCh38.p7	11:1288783	GAAGGCTCTCTGCGG[A/G]AGACAAGAGGGAGAG	54472
rs755460687	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288295	AGCTGGACCCTAAGG[A/G]CAGAGCTTGGAAGGG	54472
rs755555553	snp	A/G	1.93508e-05	0.00311047	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290193	CACGCTCAGCCACGT[A/G]CAGCCTCCATAATAG	54472
rs755566728	snp	C/G	3.74665e-05	0.00432803	intron-variant	TOLLIP	GRCh38.p7	11:1295822	GGACCAGAGAGGCCA[C/G]TGAGTCAGGGTGGGG	54472
rs755638226	snp	A/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301445	CTGAGATCGCACATG[A/T]GTCGCGGGCTTCCGA	54472
rs755652801	snp	A/G	7.3373e-05	0.00605649	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286033	GCCAACGCCCTGCTG[A/G]TACACTGTTGGCATC	54472
rs755740101	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1277402	ACCAGTCCCGCAAGA[C/T]ACCCTGGAAAGGCAA	54472
rs755763044	snp	A/T	2.783e-05	0.00373017	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295745	ACCTGCCGCTGCTGC[A/T]GTGTGGGCGTGATGC	54472
rs755806800	snp	C/T			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274004	CTAAGCATGAGCCAG[C/T]CATCACTAGGGGCTC	54472
rs756020760	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291165	AACATGGATGGCAGG[G/T]TCAAATATAAAACCT	54472
rs756046185	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1277886	ACTACACCAAGAAAA[C/T]GCTCACAAAACTCAA	54472
rs756054421	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281298	CACTGATGCGGTCAC[A/G]CTTTATTTTTGTGAA	54472
rs756335263	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297442	GGACGATCCAGGCAC[C/T]GCTTCGAGCAGTTAC	54472
rs756348964	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298344	GGGGGACAGACAGGC[A/G]ACTCATGTCCCGGAG	54472
rs756374711	snp	C/G	1.65296e-05	0.00287481	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277129	GCGGATCACCTCCTG[C/G]TCCATGTTGGGGAAC	54472
rs756485574	snp	C/T			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311438	TTCCTTGTGCACAAG[C/T]TAAATAAAGATTTCT	54472
rs756518479	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305312	TGCAGTCAGCAGGAA[C/T]GGACGCCCTCCCAGG	54472
rs756548591	snp	A/G	1.70907e-05	0.00292319	intron-variant	TOLLIP	GRCh38.p7	11:1288779	TGGAGAAGGCTCTCT[A/G]CGGGAGACAAGAGGG	54472
rs756565157	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292613	AGCATCTGCCCATTC[A/G]CTATGACTGCACACA	54472
rs756725002	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291316	TGTACCACTGCCACC[C/T]GCTCTCCTGCAGCCA	54472
rs756740577	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1292236	CCCTGTAAACTCCTT[A/T]GCAACTGCCCTATTT	54472
rs756820124	snp	A/C/T	0.00028401	0.0119132	intron-variant, utr-variant-5-prime, synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295732	GGCGTCCAGCTGGAC[A/C/T]TGCCGCTGCTGCTGT	54472
rs756843676	snp	C/T	0.000143709	0.00847549	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276690	TGCCATGAATGGAAT[C/T]GGAAGGCGCTCCACC	54472
rs756888211	in-del	-/G			intron-variant	TOLLIP	GRCh38.p7	11:1288224	CCTGCCCTGTGGGGA[-/G]GAGCCTGGTGTCCTG	54472
rs756916416	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290476	TGGGTTCTCTAGGCC[A/G]TCTGCCTCCCTGAAC	54472
rs756962046	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288326	CTGTGGGGGTCCTCC[A/G]AGGACACAGGGGCCT	54472
rs757013337	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308718	AACTGAGGTTTTGCA[A/C]GGTGGCCACTAACCG	54472
rs757063402	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276092	AGGGCCACGCTCGCC[A/G]GGCTTTCCTCGCCCA	54472
rs757073865	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299411	ATGCTTCACGAGTCA[C/T]AGGGGAGAGAGTCCA	54472
rs757128876	snp	A/C			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298503	TTTGAAGGCGTCCAG[A/C]GCTCCATCTCCTTGC	54472
rs757152762	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1283431	ATCTAGATGGCCGTA[C/T]TGTGCCAGGGACGCC	54472
rs757186826	snp	C/T	4.15584e-05	0.00455823	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286016	CCTGTGATGGGCACA[C/T]AGCCAACGCCCTGCT	54472
rs757207243	snp	C/T	0.000171615	0.00926164	intron-variant	TOLLIP	GRCh38.p7	11:1283482	GCCTGGGCATGGGGG[C/T]TGGGGGCTCCGGTGG	54472
rs757221969	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280069	AGCGACCAAGTTAGC[A/G]GGTTAATAAACACAA	54472
rs757362731	snp	A/G	6.69804e-05	0.00578668	synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290389	CATGCGGGTCATGCC[A/G]TAATTCTTGGCCAAC	54472
rs757362749	snp	A/G	1.66549e-05	0.00288568	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277030	CAAAACGGCATCGAG[A/G]CAGAGGCTCTATGGC	54472
rs757384582	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304545	GCACCCGCGCCAGGA[A/C]GGGGCGGCCGAGGTC	54472
rs757468926	snp	C/T	1.70159e-05	0.00291679	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290241	CCTCATCGAAGATCT[C/T]GAGATAGAAAGAGTC	54472
rs757526937	snp	A/G	1.66994e-05	0.00288953	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290330	TTGTGTGCCGTGGGC[A/G]TCTCGTACACCGCGT	54472
rs757689176	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293262	GGGCACACGGAGTCC[A/G]GAGTGCCCACGGAAC	54472
rs757740465	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1305415	GGGCTCTTCACAACA[C/G]TCAGGGGAGAGAAAG	54472
rs757765746	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1305942	CTCGATACTCCTCGC[C/G]GGGGCCCGCACGGTA	54472
rs757852980	snp	C/G	0.00148893	0.0272442	intron-variant	TOLLIP	GRCh38.p7	11:1283573	TTTTCTATGAAGTGC[C/G]GGGCTGTTCCAAAAT	54472
rs757867155	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308014	AGTACTGGGCTGCGC[A/G]AGGGCAGGGACCTTG	54472
rs757918277	in-del	-/G	8.64827e-05	0.00657525	intron-variant	TOLLIP	GRCh38.p7	11:1295799	CCGATGTACACCTGC[-/G]GGGCCGGGGACCAGA	54472
rs758143000	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300493	TTTTTGTCATGCAAT[A/G]TGTGTAGTCAATCCA	54472
rs758165263	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303928	GTAATCCCAGCTACT[C/T]GGGAGTCTGAGGCAG	54472
rs758206107	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297361	TCACCTGTGTCCCCA[C/T]CTAAGGCCTGGAGCG	54472
rs758303453	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275821	AGACCCACTTGTGGG[C/G]ATTCTCTTTCTGTCC	54472
rs758340141	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299466	TCAGTGACGACACTC[A/G]GTCCTTCAGTAAATG	54472
rs758378739	snp	C/G	1.80745e-05	0.00300615	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295650	CAAGGCCCACCTGTA[C/G]CACCGTGATGTTCAG	54472
rs758413376	snp	C/T	1.7403e-05	0.00294978	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290224	CTGGCACGTCCCTCT[C/T]ACCTCATCGAAGATC	54472
rs758468865	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290831	CATGATGACCCGGGA[A/G]AGGTGCATCCTCGCT	54472
rs758611901	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305470	CAACTCTCTCCTTGA[A/G]GTACGGGAAGATGAG	54472
rs758675362	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280217	TTCGCTGGAATTCCA[C/T]GTGCGAGGGGAAGCA	54472
rs758744443	in-del	-/CA			intron-variant	TOLLIP	GRCh38.p7	11:1294163	AAAGCCCGCATGGCT[-/CA]CAGTGTGTCTCCTTT	54472
rs758805454	snp	A/G	0.00012566	0.00792553	intron-variant	TOLLIP	GRCh38.p7	11:1285971	GGGGTTTCTACCAGG[A/G]GAGAGGCACCCAGGG	54472
rs758815028	snp	A/G	0.000144645	0.00850302	intron-variant	TOLLIP	GRCh38.p7	11:1295844	AGGGTGGGGGCACAA[A/G]GCAGCCCGACAGCAG	54472
rs758879462	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1296299	CAAAAGTATCCCAGA[A/G]GAACGCAGGAAGTAA	54472
rs759199631	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306654	AGAGGGGCTGGGGTG[A/G]GTCATGCTCAGCGAA	54472
rs759207750	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295576	TGCAGTATAAACGCC[A/G]AAATCCGAAATCCCA	54472
rs759284098	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285222	ATGGCCTGGGCCTCT[A/G]GCCTCCACCCTCCGT	54472
rs759330126	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290939	CCCTGCCTGTGCTAT[C/T]GGAGTACGTGGGGTT	54472
rs759333385	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1288306	AAGGGCAGAGCTTGG[-/A]AGGGCTGTGGGGGTC	54472
rs759344430	in-del	-/GAGA			intron-variant	TOLLIP	GRCh38.p7	11:1286352	AACTGGGATGTGACT[-/GAGA]GAGGATGGTGACAGG	54472
rs759445552	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307781	TCAGAGGCCGTCCAG[G/T]ACCTCTGCCGACCCG	54472
rs759488068	snp	A/C			synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277210	CACGGCGGCCGGGGG[A/C]AGGGCCACGGGCACC	54472
rs759496131	snp	C/T			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298092	TCTGCTCACCAGGAA[C/T]GGGTTATCTTGCAGA	54472
rs759537645	snp	C/T	0.000334392	0.0129261	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274611	CGGCGACCTGTCTTC[C/T]ATCTCCGGAGCCCCG	54472
rs759599269	in-del	-/C	1.83374e-05	0.00302793	intron-variant	TOLLIP	GRCh38.p7	11:1295632	GCAGGCAGGAGGGTG[-/C]CCCAAGGCCCACCTG	54472
rs759644394	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303283	GGAAAACCCCTTCTC[A/G]TTCAGATGAAACAAA	54472
rs759716943	snp	C/T	6.30034e-05	0.00561228	intron-variant	TOLLIP	GRCh38.p7	11:1277283	CAAGTTTGGTAAAAA[C/T]GTCGGAAAGTTCCAG	54472
rs759838134	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289106	CTCCTCCCCAGCCCT[C/T]GGGGCCCCATCCTTG	54472
rs759838249	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279188	TGACAATGAGGGGAT[A/G]TGGCGCCGACTGGCC	54472
rs760134367	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302351	CAGGGTTTCAGAGAC[C/T]GAAGTGCCAGCCTGC	54472
rs760209716	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286916	AAAACTGTCCACTGC[A/G]GATAAGTCACTGCAC	54472
rs760219268	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291368	TGGTGATAGAGACCC[C/T]GGGAGCCATCCCGGC	54472
rs760286482	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1287311	TCGTCACTCACGGCC[A/G]GGACATGATTTAAAA	54472
rs760460010	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283208	GCGGGGGCCCTGCCA[A/G]CAGCCCCGGGGAAAC	54472
rs760523188	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281813	GGCGACACACATGCT[C/T]TGGCCAAGATGCACT	54472
rs760671756	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299284	TACAAATACTGGTTA[C/T]GCAACCTGCTGCCCC	54472
rs760715472	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275619	AGCATGTCCCTCCCC[C/G]ACGGCCACCACACAC	54472
rs760800248	in-del	-/A	1.6676e-05	0.00288751	frameshift-variant, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288689	TCCCGCTCAGGCTGT[-/A]CCACTTGTCCTCCAC	54472
rs760961428	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308634	GCCAGGCAACTCTCA[C/G]GAGAGAATTCAGAGC	54472
rs760985550	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274939	GCAAGCTGCTTCTAC[A/G]GTAAGCCACTTCTAC	54472
rs761083128	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279908	GGCTCCAGACGTCTC[A/G]CACCACAGTGGAAAG	54472
rs761153223	snp	C/T	6.65181e-05	0.00576668	intron-variant	TOLLIP	GRCh38.p7	11:1285954	CACCTGCCCTAGGCC[C/T]TGGGGTTTCTACCAG	54472
rs761185521	snp	A/T	1.96423e-05	0.00313381	intron-variant	TOLLIP	GRCh38.p7	11:1277267	CCCTGGAAGCAAAGA[A/T]CAAGTTTGGTAAAAA	54472
rs761343792	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1278451	TCAATCCTGGCCTGA[A/G]CCAACACCAGCAACA	54472
rs761359436	in-del	-/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307947	GAAACACCAGGACTT[-/G]GTGGATACAGTGTTA	54472
rs761447147	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279141	GACGCTGCGACGTCA[C/T]GGCCTGGGGTGTCCC	54472
rs761498621	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288534	CTCAGTGCCTCCAGG[A/G]AAGAGACAAGGGTGT	54472
rs761541013	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1285511	TGCTCACTCCTAACA[C/G]TGACACACGACAACA	54472
rs761563594	snp	C/G	0.000454236	0.0150636	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276839	GAGATGGGAGGGGAG[C/G]CCCCGCCCCGTCCTG	54472
rs761623414	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293047	GGCTGAGCGGGGGCA[A/G]TGGGTGGGTGCGGGG	54472
rs761631158	snp	C/T			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310454	AACAAGAAGCATTCT[C/T]AGTTGAAGTTTCGCT	54472
rs761651237	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1284554	CGGGGTTTCACCGTG[G/T]TGGCCAGGATGGTCT	54472
rs761775355	snp	A/T	1.65644e-05	0.00287783	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277056	ATGGCTCCTCCCCCA[A/T]CTGCAGCAGGGAGTT	54472
rs761872443	snp	G/T	0.000197103	0.00992534	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309590	TGCGACGGAGACAGT[G/T]GTCACCTCGAGGCCG	54472
rs761880996	snp	C/T	3.40148e-05	0.00412386	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288628	GTGCAGCTCACCGCG[C/T]AGGACATGACGAGGT	54472
rs761923998	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285052	TGGCCTCACAGCACT[C/T]TCGCCTGCCAGCAGC	54472
rs761984410	in-del	-/C	6.49203e-05	0.00569701	intron-variant	TOLLIP	GRCh38.p7	11:1285966	GCCCTGGGGTTTCTA[-/C]CAGGGGAGAGGCACC	54472
rs762051229	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300984	GCACTTGGCATGTAA[A/G]CACTGCAAGCAAGGC	54472
rs762102583	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300351	ACTGACGCCAGAGCT[C/T]TAAACCACTGCAGCG	54472
rs762166944	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1306771	AAGTCCAGTCCTCCT[C/G]TGCCCAGGACCCTCC	54472
rs762285237	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298710	GGGGAGAAGCAGCTC[C/T]CTGCGGATGGAGCTC	54472
rs762377289	snp	C/T	1.704e-05	0.00291885	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277197	GGGGCTGGGCGTTCA[C/T]GGCGGCCGGGGGCAG	54472
rs762377396	snp	C/T	1.75391e-05	0.00296129	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295677	TCAGTCGGCCCACGG[C/T]GCCCACTGCGCCTCC	54472
rs762396044	snp	A/C	0.112256	0.20863	intron-variant	TOLLIP	GRCh38.p7	11:1288823	ATCAGGGAAGGGGCC[A/C]CCCTGCCCCTGCAGC	54472
rs762411425	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280776	CCCCAGAGGACAGCG[C/T]GGCCGGCACCACCTT	54472
rs762530134	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293079	GCTCCAGGCCTGGAC[A/G]GGCTGAAGGTGGCGC	54472
rs762560146	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305679	TATCAACGATGTGAA[A/G]AGTGAGGGGACCTGG	54472
rs762625625	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1279741	TACTGACAAACACAA[G/T]GATACCCAGGAAAAC	54472
rs762684163	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305276	TGAGGAGGCGGTGAG[C/T]GCGTTCCCCGCTGGC	54472
rs762710011	snp	A/G	1.68465e-05	0.00290223	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288763	GCAATGCGGTCGTCC[A/G]TGGAGAAGGCTCTCT	54472
rs762716399	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276168	GTCGGCTGGCAGTGC[C/T]ACCACACCCTCTCGG	54472
rs762734928	snp	A/G	3.49999e-05	0.00418315	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276804	CAGGGACAGGAGAGC[A/G]CGCTGAGACCTCCCA	54472
rs762769226	snp	A/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301170	AATAAACAACTTATA[A/T]AAACACAATAAAAAA	54472
rs762769513	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1285552	CGCAGTAGAGAGCAC[C/G]CATCACCCAACAGGA	54472
rs762771209	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289204	GCCTCCCACAGCTGA[C/T]TCTGCACTTCCCATG	54472
rs762808712	snp	A/C	5.69622e-05	0.00533646	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295784	TCCTGCGGGAGCTCA[A/C]CGATGTACACCTGCG	54472
rs762819049	snp	A/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311435	GACTTCCTTGTGCAC[A/G]AGCTAAATAAAGATT	54472
rs762865574	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286641	ACTGCTGTCTCCTGA[A/G]TTCAAAACTGTCAAC	54472
rs762911622	in-del	-/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304462	ATCTAAACAAGCGCT[-/G]ACTCGAGAGAAGTAA	54472
rs762922260	in-del	-/T			intron-variant	TOLLIP	GRCh38.p7	11:1287191	CACCACTGTCGTCTC[-/T]TGAGTTCGAAACTGT	54472
rs763010921	snp	A/G	8.39807e-05	0.00647945	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276995	GGGAGCGCCGGGTCG[A/G]CGTGTCCAAAGAGCG	54472
rs763034319	snp	C/G	0.00155279	0.0278206	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309536	CTCGCCGACCCGACA[C/G]TGACGCGCCGGGCGA	54472
rs763085247	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281711	CGTGCACACAGGCCC[A/G]AAGCCACGCAGCCAG	54472
rs763213773	snp	C/T	6.0033e-05	0.0054784	intron-variant	TOLLIP	GRCh38.p7	11:1285978	CTACCAGGGGAGAGG[C/T]ACCCAGGGAGGGAGC	54472
rs763255086	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298930	AAGGAAAGCCTGAGA[A/G]ACGGTCCCAGATTGG	54472
rs763255290	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1295884	GCATTCCCGCGGCCC[C/T]GCCCCCACCCATGTC	54472
rs763313968	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298419	CAGGGACGTGTGGGC[A/G]TGGGGTCCAGAGGCC	54472
rs763332463	snp	C/T	1.85606e-05	0.0030463	intron-variant	TOLLIP	GRCh38.p7	11:1295595	TCCGAAATCCCACCC[C/T]CACCGAGCGCACCAG	54472
rs763336098	snp	A/C/T	7.49485e-05	0.00612116	intron-variant	TOLLIP	GRCh38.p7	11:1286140	GGAGGAACATCCACC[A/C/T]ATCAGAACCTCGGGA	54472
rs763493280	snp	C/T	1.67186e-05	0.0028912	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290383	GGGGTCCATGCGGGT[C/T]ATGCCGTAATTCTTG	54472
rs763499190	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285857	TGGCCTGAAAGGATC[C/T]GTGTGCGGTCAGCAC	54472
rs763587191	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282620	CCCTAAAACTTAAAA[C/T]ATAATTAAGATAAAT	54472
rs763623332	snp	A/G	0.000115263	0.00759066	intron-variant	TOLLIP	GRCh38.p7	11:1288828	GGAAGGGGCCACCCT[A/G]CCCCTGCAGCCGCAC	54472
rs763646527	in-del	-/AA			intron-variant	TOLLIP	GRCh38.p7	11:1277423	GAAAGGCAAACCCCC[-/AA]AAACAGCAACCCCAG	54472
rs763646997	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287315	CACTCACGGCCGGGA[C/T]ATGATTTAAAATATC	54472
rs763706104	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1278367	ACTGGAGCGCTAGAG[C/G]CCCAATCTTAGGATA	54472
rs763715117	snp	C/T	0.000287646	0.0119892	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276805	AGGGACAGGAGAGCG[C/T]GCTGAGACCTCCCAG	54472
rs763753534	snp	C/T	5.72525e-05	0.00535004	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295785	CCTGCGGGAGCTCAC[C/T]GATGTACACCTGCGG	54472
rs763895447	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283247	ACCCTGCAAGGCCAC[A/G]TCAGCAGCCCCACCA	54472
rs763952628	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292188	TGCACACCCACACAT[C/T]TGCTAGATCAGCTCT	54472
rs763963866	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307796	GACCTCTGCCGACCC[A/G]TAGGCTCCACACCTG	54472
rs763995925	snp	C/T	0.000266276	0.0115355	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309561	GGGCGACCTCCTGCG[C/T]CCCCGCCGGAGCCTG	54472
rs764073212	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291272	CGGCTGCCTGTAAAG[C/T]GTCCTGCCTGGAATG	54472
rs764148191	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303638	TGCCAGGGCAGGGCC[C/T]GCAGGATCTGGAGAC	54472
rs764227120	snp	A/G	1.67052e-05	0.00289004	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290324	GCGCCATTGTGTGCC[A/G]TGGGCGTCTCGTACA	54472
rs764297378	snp	G/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300140	ATAAAAAGGACAGGG[G/T]AGGGCTCTCATCCCA	54472
rs764335602	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284530	ATTTGTTTGTATTTT[C/T]AGTAGAGACGGGGTT	54472
rs764352104	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299373	GCAAAGCCCTTCAAA[C/T]GAGGAGGGAGTGCTA	54472
rs764356549	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310352	GCTGCATCCCCAGGA[A/G]TCGGGCGTTTACGGT	54472
rs764361038	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275667	AAATATTTATCAACA[A/G]TATATTTGACAAAAA	54472
rs764384006	snp	C/T	5.07859e-05	0.00503889	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277191	TACAGCGGGGCTGGG[C/T]GTTCACGGCGGCCGG	54472
rs764463572	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305400	TGCAGGAAAATCCAC[A/G]GGCTCTTCACAACAC	54472
rs764473151	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308663	GCAGGAAAGGTTCTC[C/T]GAAGTTCCTGGCGCC	54472
rs764483427	snp	A/T	1.65241e-05	0.00287433	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277102	GTTCCCTCGCTGGGC[A/T]TCCAGCACGGAGCGG	54472
rs764545732	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1292278	TGTAGCAGGAAAGTC[A/T]GAGACCAGCATGATT	54472
rs764683709	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292385	TGAGCAAAGCCAGCT[C/T]TCTGGGTGGCACATG	54472
rs764764201	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283290	GAACATACCCTAGGA[A/G]CAAGATGGGGACCCC	54472
rs764810129	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305136	CCAAGAGGCCCGTGG[A/G]TCCCCACACAGTGAA	54472
rs764896585	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1286901	CTGTCTCCTGAGTTC[-/A]AAACTGTCCACTGCG	54472
rs764910941	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310496	GATACAGATGCTTGC[A/G]GAGGACAGGCGTTAT	54472
rs764966866	snp	C/T	0.000284981	0.0119335	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276780	CATGAGAAGGAGAGA[C/T]GCACGTCCCAGGGAC	54472
rs765041844	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275770	AAAAAGACTAAAATG[C/T]AAGCACTAACTTCCT	54472
rs765073678	in-del	-/GCT	4.80798e-05	0.00490281	intron-variant, cds-indel, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295737	CCAGCTGGACCTGCC[-/GCT]GCTGCTGTGTGGGCG	54472
rs765095016	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1284579	TGGTCTTGATCTCCT[C/G]ACCTCACGATCTGCC	54472
rs765129306	snp	A/C	0.000220192	0.0104903	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274813	TTGTGAGCTGGCAGA[A/C]AAGCCTGTCCTTCTG	54472
rs765163732	snp	C/T	5.57295e-05	0.00527841	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295711	CTGCAGCTGCTGGGC[C/T]GCCTGGGCGTCCAGC	54472
rs765279626	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1293053	GCGGGGGCAGTGGGT[G/T]GGTGCGGGGGGCTCC	54472
rs765348234	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280953	CGCACGAAGAACGCA[C/T]GGGAAATTGAGCAGT	54472
rs765365888	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1282181	TGCAGAGAGCCTGGG[A/G]CTTCCTGCAGTGCCA	54472
rs765378076	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1280104	AGAGAGTTCCATGTG[A/T]TAGTTTGTCTCGGAA	54472
rs765487474	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301036	GCCAGGTTAGCATAA[C/G]TAAGTCGAACGAAGT	54472
rs765534435	snp	A/G	4.22066e-05	0.00459364	intron-variant	TOLLIP	GRCh38.p7	11:1277284	AAGTTTGGTAAAAAC[A/G]TCGGAAAGTTCCAGA	54472
rs765578822	snp	A/G	3.33884e-05	0.00408572	stop-gained, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290361	AGCCCAGGCGCAGTC[A/G]GCAGTAGGGGTCCAT	54472
rs765673572	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306853	CTCTCCACCTCCAGA[C/T]CCCACACCTCTCTTT	54472
rs765753844	snp	C/T	5.01786e-05	0.00500867	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277020	AGAGCGGGGGCAAAA[C/T]GGCATCGAGGCAGAG	54472
rs765842689	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284715	ACACGCTCTGCTCTT[C/T]CCTCTGGAGAAAGGC	54472
rs766059349	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301274	CAAACTGACATCATT[A/G]GCGATGGGCTAAATA	54472
rs766071540	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293097	CTGAAGGTGGCGCCT[A/G]TGCTGAGGGTCAGGC	54472
rs766203053	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305278	AGGAGGCGGTGAGTG[C/T]GTTCCCCGCTGGCTC	54472
rs766211794	snp	A/G	0.000544218	0.0164867	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274577	TCTGCAGAGGGGAGA[A/G]GAGAGGAGGGGGAGC	54472
rs766263496	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303992	AGTGAGTTGAGATTG[C/T]GCCACTGCACTCCAG	54472
rs766281769	snp	C/T	1.67615e-05	0.0028949	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288648	CATGACGAGGTTGAT[C/T]ATGCCCTCCTTGTCG	54472
rs766316766	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1305584	TTACAAACAATCCCA[C/G]TTAATAAACACCGAA	54472
rs766331271	snp	A/G	3.46807e-05	0.00416403	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295687	CACGGTGCCCACTGC[A/G]CCTCCGTACTGCAGC	54472
rs766336771	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276178	AGTGCCACCACACCC[G/T]CTCGGAATCATGCAC	54472
rs766389620	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285596	ACACAACGGCGCAGC[A/G]CAGGGCACGCGTCAC	54472
rs766414183	snp	A/G	5.15681e-05	0.00507754	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277201	CTGGGCGTTCACGGC[A/G]GCCGGGGGCAGGGCC	54472
rs766415165	snp	C/T			missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277115	GCTTCCAGCACGGAG[C/T]GGATCACCTCCTGGT	54472
rs766425453	snp	A/G	2.03279e-05	0.00318803	intron-variant	TOLLIP	GRCh38.p7	11:1277275	GCAAAGATCAAGTTT[A/G]GTAAAAACGTCGGAA	54472
rs766439766	in-del	-/C	0.000458857	0.01514	intron-variant	TOLLIP	GRCh38.p7	11:1288820	GCATCAGGGAAGGGG[-/C]CCACCCTGCCCCTGC	54472
rs766450992	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1307007	AGATCACAGACCCAC[C/T]GGGCCGTCACCACAC	54472
rs766590329	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1281771	CAGGCTTCTCCACCA[A/T]GTGAGTCATAAACAC	54472
rs766643365	snp	C/G	1.85214e-05	0.00304309	intron-variant	TOLLIP	GRCh38.p7	11:1295608	CCCCACCGAGCGCAC[C/G]AGCCCCAGGCAGGCA	54472
rs766815911	snp	C/G			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297778	GTGGGCCCATGCCAG[C/G]AGTCCCAGGCCAGCC	54472
rs767009296	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1296063	TGGGTTCCTGTCCTC[A/G]AAGCCTGCTCAGGTG	54472
rs767035073	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273919	ACGCTCCAGCAACGC[A/G]TCCGTGCCCGGGTGC	54472
rs767088985	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288570	GGGCGGCATAGCCCC[A/G]ACGTGCTCCAACATA	54472
rs767157606	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286765	AACTGTCCACTGCGG[A/G]TAAGTCATTGCACTG	54472
rs767210686	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285691	GAGGTTCTCCTGCAC[A/G]GAGCTGGGCACAACG	54472
rs767250508	snp	A/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290944	CCTGTGCTATCGGAG[A/T]ACGTGGGGTTTTGGG	54472
rs767253596	snp	C/T	0.000151114	0.00869105	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276840	AGATGGGAGGGGAGC[C/T]CCCGCCCCGTCCTGG	54472
rs767255576	snp	C/T	8.37107e-05	0.00646903	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290297	ATGACCTTATTCCAG[C/T]GGGGATTCTTGGCGC	54472
rs767333579	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1295463	ATGTTTGGTAGAACC[C/T]GGGGTCAATGCCAAT	54472
rs767388195	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302189	ATCCACCCGATGCCC[A/G]CACACCTGTGTGATT	54472
rs767399615	snp	A/G	1.69571e-05	0.00291174	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288631	CAGCTCACCGCGTAG[A/G]ACATGACGAGGTTGA	54472
rs767462016	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279682	ACCTCACGTTCTTCA[C/T]GCTGTGTGAATCTGC	54472
rs767522924	snp	C/T	1.67483e-05	0.00289377	missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290393	CGGGTCATGCCGTAA[C/T]TCTTGGCCAACTTTG	54472
rs767682183	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281913	CCCTGAGCACGCAGC[C/T]GCCAGCCTCTCCAAG	54472
rs767732605	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307708	GCACTTGGCTGCCAC[A/G]GCAACTTGCGGGGAC	54472
rs767773440	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283034	GGGCGGGATCTTCAC[A/G]TGGTCCTGGGGTGCC	54472
rs767827904	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292099	TACTCCGGAATGCTA[C/T]GGAGTGACAGTTTTC	54472
rs767968862	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299102	CGGGGAGGGGAGCGT[C/T]GGCCAGGGGACATGG	54472
rs767974020	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308406	CCAGAGGCCTCCCCA[A/G]GAGCAGATGCCGGCA	54472
rs767987464	snp	A/G	3.41886e-05	0.00413438	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277198	GGGCTGGGCGTTCAC[A/G]GCGGCCGGGGGCAGG	54472
rs768032741	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275271	GCACCCCAGCAACGC[A/G]AAGGCAGAAACCGGT	54472
rs768071236	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1288303	CCTAAGGGCAGAGCT[A/T]GGAAGGGCTGTGGGG	54472
rs768075105	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299809	CCTGAGGCTGCGTCA[C/T]CTGTGCCGTCAAAAC	54472
rs768289079	snp	C/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298758	CGGGGACCGCAGCCA[C/G]CGCCATGTGGCGGGG	54472
rs768334174	snp	A/G/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275318	GGGCGCCTGGACACC[A/G/T]AAGCCCCCAGCACAG	54472
rs768385278	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276560	GCTCACAGCAAAGCG[C/G]GTTAGGGCAAGGGCG	54472
rs768430034	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291089	GGGGTGGGAGTGAAC[A/G]TGTGTTCAGAATAAG	54472
rs768444618	snp	C/T	0.00413359	0.0452737	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277049	AGGCTCTATGGCTCC[C/T]CCCCCATCTGCAGCA	54472
rs768461739	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292809	ACACAGCGCAGCAGA[C/T]GGCGTTACCACTGCA	54472
rs768680488	snp	C/T	6.67757e-05	0.00577784	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290343	GCGTCTCGTACACCG[C/T]GTAGCCCAGGCGCAG	54472
rs768705218	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279578	GGAGGAGTGATGGGC[A/G]GCTTTGCTGTGTCCC	54472
rs768718970	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298899	CGTCCTCAAACCGTC[A/G]AGGTCCCAAAAACAC	54472
rs768744957	snp	A/G	2.05489e-05	0.00320531	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276849	GGGAGCCCCCGCCCC[A/G]TCCTGGACCGCCAGG	54472
rs768890824	snp	A/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311319	AGAAGCACTAGACAA[A/G]CCCCTCCTATCCATG	54472
rs768914871	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290554	TCGCCTGAACACGGC[C/T]GTGACCTGCTTCCCA	54472
rs768971463	snp	A/C	1.85682e-05	0.00304693	intron-variant	TOLLIP	GRCh38.p7	11:1295597	CGAAATCCCACCCCC[A/C]CCGAGCGCACCAGCC	54472
rs768975507	in-del	-/TCC	1.66131e-05	0.00288206	cds-indel, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277166	TGGATGGCTTTCAGG[-/TCC]TCCTCGCTACAGCGG	54472
rs769026579	snp	C/T	7.04647e-05	0.00593527	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295674	TGTTCAGTCGGCCCA[C/T]GGTGCCCACTGCGCC	54472
rs769056964	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300037	AGGGAAACAGGCAGG[A/G]AAGATTCTATTTCAA	54472
rs769133619	snp	A/G	0.000373902	0.0136679	intron-variant	TOLLIP	GRCh38.p7	11:1283512	GGGCGTCAGGTGGAC[A/G]AGTCCTCACAGGCTC	54472
rs769175597	in-del	-/TAT			intron-variant	TOLLIP	GRCh38.p7	11:1284524	CGGCTAATTTGTTTG[-/TAT]TTTTAGTAGAGACGG	54472
rs769310531	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289740	CGGCAAGACCCTGTG[C/T]GCCCAGCGGGGCGGA	54472
rs769362054	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279646	CGCACGCGGACGGAT[A/G]TGCAGCACAGGACAG	54472
rs769551416	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293749	TCTGGAGCTTGAACT[A/G]TGTGAGGTGGAGTGC	54472
rs769583601	snp	C/T	0.000100939	0.00710346	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276993	TGGGGAGCGCCGGGT[C/T]GGCGTGTCCAAAGAG	54472
rs769586893	snp	A/G	3.37941e-05	0.00411046	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290254	CTCGAGATAGAAAGA[A/G]TCCACGCCTGGGGGC	54472
rs769590037	snp	C/G/T	0.000877463	0.0209281	intron-variant	TOLLIP	GRCh38.p7	11:1288820	GGCATCAGGGAAGGG[C/G/T]CCACCCTGCCCCTGC	54472
rs769789809	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1306409	TCACTAGGGGGAGGC[A/C]ACGGCTAGACCACAG	54472
rs769926714	snp	A/C/G	0.00108651	0.0232873	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309512	ATGGTGCTGCGGCGG[A/C/G]CCCCGTGGCTCGCCG	54472
rs769990375	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305270	GACTCGTGAGGAGGC[A/G]GTGAGTGCGTTCCCC	54472
rs769991375	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276937	CGGGAGGGGGCGACA[C/T]GGGTGCTCTTTCACG	54472
rs769993275	snp	A/G	3.32629e-05	0.00407803	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277034	ACGGCATCGAGGCAG[A/G]GGCTCTATGGCTCCT	54472
rs770016344	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274497	GGACCCCAGTAAAAT[A/C]ATCAGAAGCGCACGT	54472
rs770025043	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301858	AGAGAGAAATAAATC[C/T]CCCGTAGTAGGAACA	54472
rs770050518	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1306974	CCATTTACAAACTCT[-/C]CCAGCACCTGACGCT	54472
rs770099049	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286317	GAGGTGACATGGCTC[A/G]GGCTTACAGACCCCC	54472
rs770173867	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1307411	CCCACTTCCTCATCG[A/C]GGGTGTAACAGCGCT	54472
rs770286623	snp	C/T	1.78055e-05	0.00298369	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295667	ACCGTGATGTTCAGT[C/T]GGCCCACGGTGCCCA	54472
rs770420666	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291886	GGCTGTCCCGTCCAC[A/G]CCAACCCTCGCCGCA	54472
rs770422514	snp	A/G	0.000121094	0.00778024	intron-variant	TOLLIP	GRCh38.p7	11:1288618	CCGCCCAGGCGTGCA[A/G]CTCACCGCGTAGGAC	54472
rs770426227	snp	C/T	0.00018365	0.00958078	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277175	TTCAGGTCCTCCTCG[C/T]TACAGCGGGGCTGGG	54472
rs770431240	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281448	CAGCTTGCACTCTCC[A/G]TAGAGGTGGCAGCTG	54472
rs770473731	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290818	CCTGCCCCCGGAGCA[C/T]GATGACCCGGGAGAG	54472
rs770549876	in-del	-/GAC			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300318	CGCAAGCCTGTGACT[-/GAC]GACCATTCCTCCCTC	54472
rs770563507	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1295211	TAAGCAACCACGGGC[C/T]GGCCCCGAGGCTGAC	54472
rs770587684	snp	A/G	1.74042e-05	0.00294988	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290452	GAGGTGCCAACCATC[A/G]GGAGAGGGTGGGTTC	54472
rs770600258	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306488	TCTTTCTGCTGGAAA[A/G]CTGAGCGAGCGCCCT	54472
rs770718419	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1278173	GAGCAGCCCTGAGCA[A/C]AGGCAGCGTGCGCGG	54472
rs770727408	snp	A/G	3.61135e-05	0.00424917	intron-variant	TOLLIP	GRCh38.p7	11:1288814	GCCCCAGGCATCAGG[A/G]AAGGGGCCACCCTGC	54472
rs770770955	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1286653	TGAGTTCAAAACTGT[A/C]AACTGTGGATAAGTC	54472
rs770918842	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295207	CCACTAAGCAACCAC[A/G]GGCCGGCCCCGAGGC	54472
rs770942485	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292004	TCACTTCTAATCAAA[A/G]CTGTGGCCGGTCCTT	54472
rs770995599	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303244	TGCATCCTAAGTGCT[A/G]GGACGGTCAAGCAAG	54472
rs771092450	snp	A/G	3.80916e-05	0.00436398	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295765	GGGCGTGATGCGGAG[A/G]AAGTCCTGCGGGAGC	54472
rs771193459	snp	G/T	3.44382e-05	0.00414945	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276880	AACCGAAAACCCACA[G/T]GCACCCAAGAACAGG	54472
rs771337221	snp	C/T	5.18175e-05	0.0050898	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309430	CCCGCAACCGCAGGT[C/T]ACCGCCCCCGCCCGA	54472
rs771367841	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305029	GTAAAATCATAGAAG[A/G]AAAAAGTACTAGGTG	54472
rs771372814	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276021	GCCAAGATGCTACAC[A/G]CAGCGCCCAGGCAGT	54472
rs771413256	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308417	CCCAGGAGCAGATGC[C/T]GGCACCATGCTACCT	54472
rs771437658	snp	C/T	6.69411e-05	0.00578499	intron-variant	TOLLIP	GRCh38.p7	11:1285955	ACCTGCCCTAGGCCC[C/T]GGGGTTTCTACCAGG	54472
rs771495222	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279245	CCAACACACTCACTT[A/G]GGGAGCAGGCACCCC	54472
rs771579764	snp	A/C			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274350	TGAATTAAGTTAAAA[A/C]ATACTCGGGAACAAA	54472
rs771607986	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282745	TGTAACAAACCTGCA[C/T]GTTGTGCACATGTAC	54472
rs771630136	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1297641	CCTGTGAGAGAAGCC[A/G]TACTGCGAGAACAAG	54472
rs771667248	snp	A/G	1.66946e-05	0.00288912	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290353	CACCGCGTAGCCCAG[A/G]CGCAGTCGGCAGTAG	54472
rs771676395	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306667	TGGGTCATGCTCAGC[A/G]AAGCAGGCTGGTGCC	54472
rs771720197	snp	C/G	1.65436e-05	0.00287602	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277067	CCCATCTGCAGCAGG[C/G]AGTTGATGGCGGCAT	54472
rs771720658	snp	A/G	1.72133e-05	0.00293366	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290440	TGTCAGGAAAAGGAG[A/G]TGCCAACCATCAGGA	54472
rs771730262	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282325	ATAAGGGATTCTGAC[C/T]CAAGGAAAAAAATAG	54472
rs771882334	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303456	GTGCTGGGGCACCCC[G/T]GCTCCTGGGATGCTT	54472
rs772058499	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1284319	CTTTCCTCGGTGACG[A/G]GGTGCAGGTGCTACC	54472
rs772085030	in-del	-/CA			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300154	GTAGGGCTCTCATCC[-/CA]CAGAGCTCACAGCAT	54472
rs772120928	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1278268	ACAGAGCTCCTCCTG[C/T]AGCAGCAGCTGCAGC	54472
rs772126719	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288839	CCCTGCCCCTGCAGC[C/T]GCACCATCGTGGGCC	54472
rs772129338	snp	A/T	1.66228e-05	0.0028829	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277166	TGGATGGCTTTCAGG[A/T]CCTCCTCGCTACAGC	54472
rs772140957	snp	A/C	3.50594e-05	0.0041867	intron-variant	TOLLIP	GRCh38.p7	11:1288802	CAAGAGGGAGAGGCC[A/C]CAGGCATCAGGGAAG	54472
rs772148346	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1293484	AACAAGGGGAAGCAG[C/T]GAGGGGACGCAAGCA	54472
rs772152476	snp	C/T	1.66782e-05	0.0028877	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288737	ACTCCGGGATGGTGA[C/T]GTGGGTCCAGGCAAT	54472
rs772176226	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1287307	CACATCGTCACTCAC[A/G]GCCGGGACATGATTT	54472
rs772261080	snp	C/T	3.10573e-05	0.00394052	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295753	CTGCTGCTGTGTGGG[C/T]GTGATGCGGAGGAAG	54472
rs772273048	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1292714	ACAACGGGCAAGAGA[A/C]GCACGTCAGACAGCA	54472
rs772340970	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300777	TGCCAGGAGACATCA[C/T]CCCAAGGAGCCGCAC	54472
rs772343571	in-del	-/A	0.000194313	0.00985489	intron-variant	TOLLIP	GRCh38.p7	11:1285968	CCTGGGGTTTCTACC[-/A]GGGGAGAGGCACCCA	54472
rs772383397	snp	C/T	9.24855e-05	0.00679957	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277251	TACAGACAGCGGGCA[C/T]CCCTGGAAGCAAAGA	54472
rs772450266	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289182	GACTGGAAAGGACAC[A/G]GGGTCTGCCTCCCAC	54472
rs772606653	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276059	AAGTGAGCGCCTCCC[A/G]CCTCAGAAAGCTTTT	54472
rs772622731	snp	A/G	1.7403e-05	0.00294978	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295682	CGGCCCACGGTGCCC[A/G]CTGCGCCTCCGTACT	54472
rs772744383	snp	A/G	8.34759e-05	0.00645995	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290355	CCGCGTAGCCCAGGC[A/G]CAGTCGGCAGTAGGG	54472
rs772816013	snp	A/G			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311388	CCACCCCCTGGCGGC[A/G]GGGCCCCCCACCGTT	54472
rs772847038	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1305597	CAGTTAATAAACACC[G/T]AAGAAGTGATAAAGT	54472
rs772890199	snp	C/T	1.66793e-05	0.0028878	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277173	CTTTCAGGTCCTCCT[C/T]GCTACAGCGGGGCTG	54472
rs772949834	snp	A/G	5.0229e-05	0.00501118	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290298	TGACCTTATTCCAGC[A/G]GGGATTCTTGGCGCC	54472
rs772971966	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276156	AAGCTGTCAGCAGTC[A/G]GCTGGCAGTGCCACC	54472
rs772987032	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295868	ACAGCAGCTGCCCCC[A/G]GCATTCCCGCGGCCC	54472
rs773056185	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289480	CTGCAGGTGCAGCCA[C/T]GGACGGGACTCAGGA	54472
rs773105923	snp	G/T	0.000141955	0.00842361	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276759	CAAGAGCATTTTCCA[G/T]AACGGCATGAGAAGG	54472
rs773107962	in-del	-/CTT	1.67237e-05	0.00289164	cds-indel, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288657	GTTGATCATGCCCTC[-/CTT]GTCGTCCCCCTGCCT	54472
rs773108179	snp	A/T	1.66907e-05	0.00288879	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288743	GGATGGTGATGTGGG[A/T]CCAGGCAATGCGGTC	54472
rs773382907	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301943	TCTGCTAGGAAGGGA[A/G]CCCCAGACTCGGTCA	54472
rs773414168	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290845	AGAGGTGCATCCTCG[C/T]TCTAGGTGAGAGTGA	54472
rs773429643	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288294	CAGCTGGACCCTAAG[A/G]GCAGAGCTTGGAAGG	54472
rs773491764	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276991	CTTGGGGAGCGCCGG[A/G]TCGGCGTGTCCAAAG	54472
rs773537408	snp	C/T	1.73924e-05	0.00294888	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295684	GCCCACGGTGCCCAC[C/T]GCGCCTCCGTACTGC	54472
rs773540448	in-del	-/AGG			intron-variant	TOLLIP	GRCh38.p7	11:1279085	TGATGGGGAAGGGAC[-/AGG]AGGAGGGGAACTGCT	54472
rs773710266	snp	A/G	1.90293e-05	0.00308453	intron-variant	TOLLIP	GRCh38.p7	11:1277260	CGGGCATCCCTGGAA[A/G]CAAAGATCAAGTTTG	54472
rs773801820	snp	A/G	3.19514e-05	0.00399684	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295754	TGCTGCTGTGTGGGC[A/G]TGATGCGGAGGAAGT	54472
rs773864199	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281732	ACGCAGCCAGCACCG[C/T]GTAGCCAGGCAGAGC	54472
rs773956914	snp	C/T	1.67863e-05	0.00289704	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277009	GGCGTGTCCAAAGAG[C/T]GGGGGCAAAACGGCA	54472
rs773988681	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295990	GGCCTGGCCCCCAGC[A/G]GTACAGGTGCAGCCC	54472
rs774078781	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305702	GGACCTGGACAGGAA[C/T]AGGCCTCTCAGGGAG	54472
rs774220236	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291103	CGTGTGTTCAGAATA[A/C]GACAGAAGACCGTGG	54472
rs774377465	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281796	AAACACTTGAAACTG[C/T]GGGCGACACACATGC	54472
rs774432292	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1297631	TGACCTTTGCCCTGT[A/G]AGAGAAGCCGTACTG	54472
rs774633513	snp	A/G	8.51752e-05	0.00652536	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288627	CGTGCAGCTCACCGC[A/G]TAGGACATGACGAGG	54472
rs774743394	snp	A/C/G	3.67089e-05	0.00428408	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277246	GGGGCTACAGACAGC[A/C/G]GGCATCCCTGGAAGC	54472
rs774785537	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284317	TTCTTTCCTCGGTGA[C/T]GGGGTGCAGGTGCTA	54472
rs774847653	snp	C/G	1.8561e-05	0.00304633	intron-variant	TOLLIP	GRCh38.p7	11:1295598	GAAATCCCACCCCCA[C/G]CGAGCGCACCAGCCC	54472
rs774941253	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275500	GGGAATCCCAGGGGC[C/T]CCTCCGTCTGAGTGG	54472
rs774949064	snp	A/G			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297727	ACCCCCTGCCCTTAC[A/G]GACAATCGAGGAGGG	54472
rs775016530	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1307315	GGAAACAGCCCAGGA[A/G]GCACTGGGCAAGAGG	54472
rs775065741	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274583	GAGGGGAGAGGAGAG[A/G]AGGGGGAGCCTCCGG	54472
rs775250164	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292150	GCATGCTCAGCCTCT[A/G]GCAGCTTCCAATTCC	54472
rs775397228	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1285281	CCAGCTCCCCAGAAC[A/G]AGAGAGGCCACCTCA	54472
rs775506012	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279064	TCTCTCCAGCCTTTA[C/T]CAGTCTGATGGGGAA	54472
rs775579068	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283089	CCCGGGGAACAGCCA[A/G]GCAGAGCCCGCCGTG	54472
rs775607066	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275591	CCCACAGCTGAAGAA[G/T]GCGCCTGCTGCCAGC	54472
rs775632629	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288430	AGAACATGGGCAGGA[A/G]CAGTGGGCAGGGCAG	54472
rs775681599	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1281590	AGCTGAATGAACGAG[C/T]GGCTGAAGGGGCTGG	54472
rs775690258	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1292755	GGACACACGGGCACC[G/T]CTGCTTTCCCCACAA	54472
rs775712183	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310294	CCAACCAGAGCGACT[C/G]CAGCTCGAACAGCGC	54472
rs775765525	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308623	TAGAAGAAACTGCCA[A/G]GCAACTCTCAGGAGA	54472
rs775788200	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303535	ATGCTAACGGCAGGA[A/G]GCGCTGTGCAAAGAA	54472
rs775795961	snp	C/G	5.06855e-05	0.0050339	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295779	GGAAGTCCTGCGGGA[C/G]CTCACCGATGTACAC	54472
rs775919908	snp	A/G	1.66938e-05	0.00288905	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290362	GCCCAGGCGCAGTCG[A/G]CAGTAGGGGTCCATG	54472
rs775972833	snp	C/T	6.6107e-05	0.00574884	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277086	TGATGGCGGCATCCT[C/T]GTTCCCTCGCTGGGC	54472
rs776090376	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1284439	CTGCAAGCTCCACCT[C/G]CTGGGTTCACACCAT	54472
rs776207180	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1295415	CTACACAGAGCAGAC[A/G]CCCACCTACACCCAC	54472
rs776256118	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285189	CCCTAGCGCCCTGCC[C/T]GCAACTTGGCCACTT	54472
rs776278589	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293662	CCTGTGGTGGGCTCC[A/G]GGGTGCGGGAGAGGA	54472
rs776280277	snp	C/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298876	GACAAAATCCCTGAC[C/G]AGTCAGTCGTCCTCA	54472
rs776399459	snp	A/G	0.000110195	0.00742195	intron-variant	TOLLIP	GRCh38.p7	11:1288816	CCCAGGCATCAGGGA[A/G]GGGGCCACCCTGCCC	54472
rs776450739	snp	A/G	0.000284455	0.0119225	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276773	AGAACGGCATGAGAA[A/G]GAGAGACGCACGTCC	54472
rs776554465	snp	C/T	3.35374e-05	0.00409482	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288754	TGGGTCCAGGCAATG[C/T]GGTCGTCCATGGAGA	54472
rs776624473	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1285967	CCCTGGGGTTTCTAC[C/G]AGGGGAGAGGCACCC	54472
rs776821338	snp	A/C	4.18945e-05	0.00457662	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295770	TGATGCGGAGGAAGT[A/C]CTGCGGGAGCTCACC	54472
rs776836443	snp	A/C			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300917	GTTCCCACCCCATGA[A/C]GCTGCGAGGCTGTGG	54472
rs776885230	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303142	GAGTACAGGACAGAA[C/T]GAGAATAAGCATAGA	54472
rs776893062	snp	A/C			upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311369	TGTGAAACTAACCCA[A/C]GTGCCACCCCCTGGC	54472
rs776907739	snp	A/C	0.000541272	0.0164421	missense, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309471	GCTGCCTCACCGGCC[A/C]GCGCTGAGTGCTGAC	54472
rs776947983	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1279253	CTCACTTGGGGAGCA[C/G]GCACCCCCGGGGGAA	54472
rs777007400	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290080	TCCTTGGGGAGAGCA[A/G]GACCCTGTCATGCAC	54472
rs777020468	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1281534	AGCCCCCGAGACCTG[C/G]ACCCTGTGCGGGGGT	54472
rs777044667	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300918	TTCCCACCCCATGAC[A/G]CTGCGAGGCTGTGGA	54472
rs777046915	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1306728	AACACTTTACAGAGT[C/G]CTGCGCTGAGCCGGT	54472
rs777213812	snp	C/T	5.39593e-05	0.00519391	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295654	GCCCACCTGTACCAC[C/T]GTGATGTTCAGTCGG	54472
rs777263539	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1281399	AAGTGGACGGTCCTC[G/T]TGAGGGCTCAGCCAG	54472
rs777299495	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300750	GAACACATGCAGTCC[C/T]GGCCTCACGCCTGCC	54472
rs777358348	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289753	TGCGCCCAGCGGGGC[A/G]GACACATGCATGCTC	54472
rs777435443	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306264	CTGGCTAGCTTCACA[C/T]GTCCTCTCCACACCT	54472
rs777489826	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1283575	TTCTATGAAGTGCGG[G/T]GCTGTTCCAAAATTT	54472
rs777491500	in-del	-/G	0.000552029	0.0166045	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309510	CCATGGTGCTGCGGC[-/G]GCCCCCGTGGCTCGC	54472
rs777604288	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297478	CAGGACCCCCAAGTT[C/T]GGGAAGCTCTCTGCA	54472
rs777606086	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274397	TTAAAGGACTTTATT[C/T]CTCTATTTTTATATG	54472
rs777616624	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276623	CCACAGTGTGAGGGA[C/T]TGTGTGTGCCTTAAA	54472
rs777644883	snp	C/T			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274175	GGAAGAGCAGACCCA[C/T]GCCCACTGCCACTGT	54472
rs777645548	snp	A/C	4.35701e-05	0.00466724	intron-variant	TOLLIP	GRCh38.p7	11:1277289	TGGTAAAAACGTCGG[A/C]AAGTTCCAGAAGTGC	54472
rs777692372	snp	G/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299559	GATGGAGGAACTATT[G/T]CAATGGTCACATAAA	54472
rs777703622	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303038	GCTCTGCTAAAGTCT[C/G]AAAGCAAACACTAGA	54472
rs777772934	snp	C/G	1.71876e-05	0.00293147	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290232	TCCCTCTCACCTCAT[C/G]GAAGATCTCGAGATA	54472
rs777801988	snp	A/G/T			intron-variant	TOLLIP	GRCh38.p7	11:1288319	GGAAGGGCTGTGGGG[A/G/T]TCCTCCGAGGACACA	54472
rs777817100	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1307214	ACCTTCTTAAGAGAC[C/T]CTGGCAGCTCCGAGC	54472
rs777860701	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1278912	AGGCGGGCAGGAACT[C/T]GGCCATCACCTGTCC	54472
rs777868416	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1306420	AGGCAACGGCTAGAC[C/G]ACAGTCAGGGTCTCC	54472
rs777876240	snp	C/T	1.75925e-05	0.00296579	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277222	GGGCAGGGCCACGGG[C/T]ACCATGCCGGGGCTA	54472
rs777978307	snp	C/G	0.000154707	0.00879372	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309423	GGCCCCGCCCGCAAC[C/G]GCAGGTCACCGCCCC	54472
rs777978898	snp	A/G	0.000148732	0.00862229	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276859	GCCCCGTCCTGGACC[A/G]CCAGGAACCGAAAAC	54472
rs778002091	snp	A/G	1.76083e-05	0.00296712	intron-variant	TOLLIP	GRCh38.p7	11:1288804	AGAGGGAGAGGCCCC[A/G]GGCATCAGGGAAGGG	54472
rs778039315	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288904	CTCCCACCTGCACCA[A/G]CACCCCATCGATGAG	54472
rs778119896	snp	A/C/G	0.000116661	0.00763662	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277027	GGGCAAAACGGCATC[A/C/G]AGGCAGAGGCTCTAT	54472
rs778149966	snp	A/C	7.63126e-05	0.00617661	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286083	GCATCACCATGGCAG[A/C]TGGAAGCAGCTGAAA	54472
rs778210720	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298365	TGTCCCGGAGACAGC[A/G]GCATGGAGAAGCCAG	54472
rs778351050	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304459	GAAATCTAAACAAGC[A/G]CTGACTCGAGAGAAG	54472
rs778378867	in-del	-/CGCCGGA			intron-variant	TOLLIP	GRCh38.p7	11:1280671	GCCAGGCTGGGGAGG[-/CGCCGGA]CGCCCCACTTTCCAG	54472
rs778380034	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292631	ATGACTGCACACAAC[C/T]ACATGCTGTTCTGGT	54472
rs778692383	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302818	GTGACTTTGTCCCCA[A/G]TTCCCACATCCTCCT	54472
rs778792958	snp	C/T	1.82058e-05	0.00301705	intron-variant	TOLLIP	GRCh38.p7	11:1295641	AGGGTGCCCCAAGGC[C/T]CACCTGTACCACCGT	54472
rs778819526	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299416	TCACGAGTCACAGGG[A/G]AGAGAGTCCAGGTGC	54472
rs778867436	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274234	CTCTAATTCAATCTG[A/G]GAAGCAAAGGCCAGG	54472
rs778938620	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1305441	GAAAGCCCACACACA[A/T]CTACAAAGAAAAGCA	54472
rs779024062	snp	A/C	1.7169e-05	0.00292988	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290435	GCCAATGTCAGGAAA[A/C]GGAGGTGCCAACCAT	54472
rs779063448	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304573	GTCTCCGCGTGGATC[C/T]GGAGGTGGCACAGAC	54472
rs779088825	snp	A/G	6.8956e-05	0.00587139	intron-variant	TOLLIP	GRCh38.p7	11:1288788	CTCTCTGCGGGAGAC[A/G]AGAGGGAGAGGCCCC	54472
rs779129491	snp	A/G			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311074	AAGCCCCTTCCTCAA[A/G]TTGTAGCTTAACATC	54472
rs779176763	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285898	TTCTAGAATGGATGA[C/T]GTCCCCACCCCGGCG	54472
rs779251563	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1278991	GCCATCGCCTGTCCC[G/T]GCCCACACGTCTCCC	54472
rs779332552	snp	A/G	0.000417673	0.0144451	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288663	CATGCCCTCCTTGTC[A/G]TCCCCCTGCCTCCCG	54472
rs779418015	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285196	GCCCTGCCCGCAACT[C/T]GGCCACTTCCATGGC	54472
rs779418567	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287405	CTGCTGCCTCCCCGC[C/T]GCAGCCTCCCCGCCG	54472
rs779517141	snp	C/T			upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309701	CCCTTCCGGCTCTCG[C/T]GCGCACGCGCGCTCC	54472
rs779585038	snp	A/C	0.000153716	0.00876552	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276722	CCTCCAACACCCTGG[A/C]AGAAGCAGCTGCTCT	54472
rs779593872	snp	C/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298736	AGCTCATCAGCCCCA[C/G]GCAGCCCGGGGACCG	54472
rs779642849	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1282359	ATTGTTTAGGAGAAA[C/T]ACCTAATGTTAAATG	54472
rs779689281	snp	A/G	0.000132635	0.00814247	intron-variant	TOLLIP	GRCh38.p7	11:1295832	GGCCAGTGAGTCAGG[A/G]TGGGGGCACAAAGCA	54472
rs779750383	snp	C/T	1.70496e-05	0.00291967	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290425	CTGGAATGAAGCCAA[C/T]GTCAGGAAAAGGAGG	54472
rs779825248	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299981	CATAAGGAGGCCTCT[C/G]TCGACACCAACTCTG	54472
rs779870113	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289485	GGTGCAGCCACGGAC[A/G]GGACTCAGGACCCTC	54472
rs779882402	snp	C/T	0.00010019	0.00707709	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290341	GGGCGTCTCGTACAC[C/T]GCGTAGCCCAGGCGC	54472
rs779907424	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275965	AGCTTCTCAAATTTC[C/T]GACTGTCATAACCAG	54472
rs779921833	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299547	TTGCCATATGATGAT[A/G]GAGGAACTATTTCAA	54472
rs779936024	snp	A/G	1.66247e-05	0.00288307	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277035	CGGCATCGAGGCAGA[A/G]GCTCTATGGCTCCTC	54472
rs780149859	snp	C/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274055	CCACGGTCCCAGTGG[C/G]CTCTCTCAGAACGGG	54472
rs780158081	snp	C/T	1.65299e-05	0.00287483	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277131	GGATCACCTCCTGGT[C/T]CATGTTGGGGAACAT	54472
rs780248364	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306975	CATTTACAAACTCTC[C/T]CAGCACCTGACGCTT	54472
rs780256994	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301649	GAACAAGCGTCAAGG[A/G]CTCCTGAAGCCACAA	54472
rs780257979	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305474	TCTCTCCTTGAGGTA[C/T]GGGAAGATGAGGGAA	54472
rs780309998	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300640	ACCTGTTAGGAATAC[A/G]TTTCCGACTGAGAGT	54472
rs780318280	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1277558	AGTCTGTTTTATAAC[A/T]AGCAGGCTGGGGGTG	54472
rs780483707	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280323	TGCATGGTGCCACCG[C/T]GTGCACGTTCTCTAT	54472
rs780539691	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276785	GAAGGAGAGACGCAC[A/G]TCCCAGGGACAGGAG	54472
rs780628940	snp	C/T	0.000143421	0.00846698	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276697	AATGGAATCGGAAGG[C/T]GCTCCACCACCTCCA	54472
rs780637471	snp	G/T	0.000187564	0.00968231	intron-variant	TOLLIP	GRCh38.p7	11:1283497	CTGGGGGCTCCGGTG[G/T]GGCGTCAGGTGGACG	54472
rs780661093	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300704	GACAGAGCCCCGGAA[A/G]AGCCCAGCTCAGCCC	54472
rs780732936	snp	A/T	8.34676e-05	0.00645963	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288703	TACCACTTGTCCTCC[A/T]CCTTGCCCTGCCTCA	54472
rs780776582	in-del	-/AACCC			intron-variant	TOLLIP	GRCh38.p7	11:1281099	AAATTGAGGCTAAAA[-/AACCC]AACCCCCTATAACCA	54472
rs780858700	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1287270	TGAAAGCGTCTGTTA[A/G]AGACGTGTCATGAGA	54472
rs780899434	snp	A/G	3.55107e-05	0.00421356	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295669	CGTGATGTTCAGTCG[A/G]CCCACGGTGCCCACT	54472
rs781028380	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306274	TCACACGTCCTCTCC[A/G]CACCTACCCACCCGG	54472
rs781186627	snp	A/C	1.66504e-05	0.0028853	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277031	AAAACGGCATCGAGG[A/C]AGAGGCTCTATGGCT	54472
rs781396054	in-del	-/T			intron-variant	TOLLIP	GRCh38.p7	11:1292405	GGTGGCACATGGGAC[-/T]CCCCTGCCAGCATGC	54472
rs781418715	snp	C/T	1.70362e-05	0.00291853	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276885	AAAACCCACATGCAC[C/T]CAAGAACAGGTGTGG	54472
rs781483413	snp	A/G	8.61289e-05	0.00656179	intron-variant	TOLLIP	GRCh38.p7	11:1295799	CCGATGTACACCTGC[A/G]GGGCCGGGGACCAGA	54472
rs781671896	snp	C/T	1.66754e-05	0.00288746	stop-gained, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288690	CCCGCTCAGGCTGTA[C/T]CACTTGTCCTCCACC	54472
rs781674775	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291871	GACCCCCGAGGGCAC[A/G]GCTGTCCCGTCCACG	54472
rs781709423	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1277772	TTGGCAAGTGTGTCA[C/G]TAAACTGTGTGCCGG	54472
rs781743709	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305035	TCATAGAAGGAAAAA[A/G]TACTAGGTGAATACT	54472
rs781782582	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306838	CCCTGGGGCTCCCTC[C/T]TCTCCACCTCCAGAC	54472
rs796087440	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290786	GCTGAGAGCCAGAGC[A/G]TGACATGGAGTGTGA	54472
rs796201078	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304622	TATTTATTCTTTAGC[C/T]GGGCAGCCTCCGGAG	54472
rs796294448	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308865	GGGCCATCAGGGTGC[C/G]GGACCCGCCTCCACC	54472
rs796325427	in-del	-/GGGAGA			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274140	CAGAACCACCCAGTG[-/GGGAGA]GGGAGAGGGTGCCTG	54472
rs796345073	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1294249	TCTACGAAAGCCCGC[A/G]TGGCTCACAGTGTGT	54472
rs796400614	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308868	CCATCAGGGTGCGGG[A/G]CCCGCCTCCACCTGG	54472
rs796510139	in-del	-/GCTCATC			intron-variant	TOLLIP	GRCh38.p7	11:1278728	AAGCATCATCCCCAT[-/GCTCATC]AGCCTTTCGGCAATG	54472
rs796521391	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1278735	ATCCCCATGCTCATC[A/T]GCCTTTCGGCAATGA	54472
rs796577306	in-del	-/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299422	TCACAGGGGAGAGAG[-/T]TCCAGGTGCTGAAGT	54472
rs796611052	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283786	CCAGTTGATGGAACT[A/G]CACCCCCCAAAAAGA	54472
rs796616842	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302910	TGTCTCCCCTTCCGG[A/G]GCCTTCCTCAGACAG	54472
rs796652025	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286399	TGTAGGTGTCGAGTC[A/G]GCCTGGGGGGAACCA	54472
rs796714153	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1278449	CTTCAATCCTGGCCT[A/G]AACCAACACCAGCAA	54472
rs796812074	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1284933	AGGTGGGTCTAGGGC[A/G]AGGTCCCGACTCCCA	54472
rs796854154	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285560	AGAGCACGCATCACC[C/T]AACAGGAGCGTGAGG	54472
rs796861560	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1295431	CCACCTACACCCACT[-/A]ACTCATCACTTGAGT	54472
rs796978247	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308869	CATCAGGGTGCGGGA[A/C]CCGCCTCCACCTGGG	54472
rs796997564	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1305617	AGTGATAAAGTTCAG[A/T]AACTACCCTCTGCCA	54472

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