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
rs908225	snp	C/T	0.469346	0.119947	intron-variant	TOLLIP	GRCh38.p7	11:1291999	TCCTTTCACTTCTAA[C/T]CAAAGCTGTGGCCGG	54472
rs2271599	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298116	TTGCAGAAACAGACT[C/T]GTGCTAACCAAGTTC	54472
rs2292635	snp	C/T	0.0973687	0.197999	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289915	GTGCACGCTCTGTCC[C/T]TGGAAATCCCACCTG	54472
rs3168046	snp	C/T	0.481627	0.0940692	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275419	AATGAAGGTGTCAGG[C/T]GGGACTGGAACGTTC	54472
rs3750920	snp	C/T	0.480178	0.0975602	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288726	CTGCCTCAGGGACTC[C/T]GGGATGGTGATGTGG	54472
rs3793962	snp	C/G	0.174288	0.23826	intron-variant	TOLLIP	GRCh38.p7	11:1278274	CTCCTCCTGCAGCAG[C/G]AGCTGCAGCAGTGCA	54472
rs3793963	snp	C/T	0.176861	0.239062	intron-variant	TOLLIP	GRCh38.p7	11:1280678	TGGGGAGGCGCCGGA[C/T]GCCCCACTTTCCAGG	54472
rs3793964	snp	C/T	0.469839	0.119042	intron-variant	TOLLIP	GRCh38.p7	11:1280752	CAGGAGGAGGGAAAG[C/T]GAGGAGGGCCCCAGA	54472
rs3793965	snp	C/T	0.481319	0.0948228	intron-variant	TOLLIP	GRCh38.p7	11:1281477	TGGGCTCAGACACCA[C/T]GGGAGGCTCTCGGGG	54472
rs3793966	snp	C/T	0.495855	0.045338	intron-variant	TOLLIP	GRCh38.p7	11:1281718	ACAGGCCCGAAGCCA[C/T]GCAGCCAGCACCGCG	54472
rs3793967	snp	C/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1285002	CTGGGGTGCTGACCA[C/G]GCCTCTCCACTCCAG	54472
rs3793968	snp	C/T	0.126219	0.217206	intron-variant	TOLLIP	GRCh38.p7	11:1294063	TTTCTATGAAAGCCG[C/T]GTGGCTCACAGTGTG	54472
rs3793969	snp	A/T	0.487995	0.0765403	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297654	CCGTACTGCGAGAAC[A/T]AGCAGAGCACCCCGG	54472
rs3793970	snp	C/T	0.485118	0.0849685	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297667	ACAAGCAGAGCACCC[C/T]GGCTTCACCTCCGGA	54472
rs3817288	snp	A/C/G/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1285909	GGGGCTTAGAGCGCC[A/C/G/T]GGGTGGGGACGTCAT	54472
rs3829223	snp	C/T	0.495999	0.0445491	intron-variant	TOLLIP	GRCh38.p7	11:1279176	AACCTGCTCTGCTGA[C/T]AATGAGGGGATGTGG	54472
rs3838783	in-del	-/G	0.47767	0.103278	intron-variant	TOLLIP	GRCh38.p7	11:1283477	CGCATGCCTGGGCAT[-/G]GGGGCTGGGGGCTCC	54472
rs4963034	snp	C/T	0.00517822	0.0506191	intron-variant	TOLLIP	GRCh38.p7	11:1293207	AGCCACCTGCGGACA[C/T]GGGGGAGAAGCCGGG	54472
rs4963060	snp	A/G	0.299411	0.245069	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299830	CCGTCAAAACGCCCC[A/G]TCCACCAGCCAGGCA	54472
rs4963061	snp	A/G	0.333722	0.235565	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303350	CCAGAGAGGGACGGC[A/G]TGTGACGTGGCAGGC	54472
rs4963062	snp	A/G	0.332568	0.235971	intron-variant	TOLLIP	GRCh38.p7	11:1305411	CCACGGGCTCTTCAC[A/G]ACACTCAGGGGAGAG	54472
rs5743851	snp	C/T	0.0588605	0.161139	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310590	GTACGCTTGTTTATA[C/T]GTAAGATAAAAGCCA	54472
rs5743852	snp	C/T	0.0228947	0.104514	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310141	GGGCTCTTCTGGCAG[C/T]GCCTCCATCCCCGTT	54472
rs5743853	snp	A/G	0.0215028	0.101435	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310128	AGNGCCTCCATCCCC[A/G]TTCCGTTCACCCGGC	54472
rs5743854	snp	C/G	0.385741	0.209939	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310024	TGAGGGAAAGATCGC[C/G]CTGCAGGGGATGTCG	54472
rs5743855	in-del	-/T/TCCCG/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGC/TCCCGGCACCCTTATGGCCCCACAGGTGGAGGCGG	0.143457	0.22616	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308834	CCCAGGTGGAGGCGG[lengthTooLong]GGGCCTGCACTCTAG	54472
rs5743856	snp	A/G	0.093417	0.194889	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308608	CTGGCAGTTTCTTCT[A/G]TAGCATTAATATTGC	54472
rs5743857	snp	C/T	0.0984431	0.198823	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308340	TTACACGTCACATGG[C/T]GAAAGCAGCAAGAGA	54472
rs5743858	snp	A/G	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308097	CAGGCTGTCGTGAGC[A/G]GTACAGTTTTTATCA	54472
rs5743859	snp	C/T	0.144296	0.226554	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308045	TGGGTGGAAAAAGTC[C/T]TTTTTCACGATGCTC	54472
rs5743860	snp	C/G	0.0252325	0.109451	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308012	AGGTCCCTGCCCTCG[C/G]GCAGCCCAGTACTGG	54472
rs5743861	snp	A/G	0.0228947	0.104514	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307953	CACCCTTAACACTGT[A/G]TCCACAAGTCCTGGT	54472
rs5743862	snp	C/T	0.0228947	0.104514	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307792	TGTGGAGCCTACGGG[C/T]CGGCAGAGGTCCTGG	54472
rs5743863	snp	C/T	0.0588605	0.161139	intron-variant	TOLLIP	GRCh38.p7	11:1307682	AGTGCTCCTTTCTGC[C/T]TAACAGGAGACTCAG	54472
rs5743864	snp	C/T	0.332337	0.236052	intron-variant	TOLLIP	GRCh38.p7	11:1307641	GAACCAGCACCCTGC[C/T]GTTGTGTCCTCCTGG	54472
rs5743865	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1307373	GGAGATGTTCTCACA[C/T]GCAGGGCCTGTGCTG	54472
rs5743866	snp	A/C/G	0.00597534	0.0543715	intron-variant	TOLLIP	GRCh38.p7	11:1307266	TATTTCAGGGGCACC[A/C/G]CCGTTGACCGGTAAA	54472
rs5743867	snp	C/T	0.333722	0.235565	intron-variant	TOLLIP	GRCh38.p7	11:1307121	ACCAACTGTGGCGTT[C/T]AGGATGGCCATGATG	54472
rs5743868	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1306926	TGTTGGGGTGAGGAC[A/G]TGACATCTCTCGGAG	54472
rs5743869	snp	G/T	0.0865458	0.189163	intron-variant	TOLLIP	GRCh38.p7	11:1306522	ACACCTGTGGTGCCA[G/T]AGAGGCAGGAGGTTA	54472
rs5743870	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306346	AAGGAGCAGAGGGGC[C/T]GCTAATGGGGTCCTG	54472
rs5743871	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1306129	CGTTTCAAAAAGGCC[A/G]GTATTTTGGAAAGAT	54472
rs5743872	snp	C/G/T	0.0494526	0.149365	intron-variant	TOLLIP	GRCh38.p7	11:1306002	CCCTGCGAGGGGTAC[C/G/T]GTGTGGACCCCTGTG	54472
rs5743873	snp	A/G	0.00953873	0.0683987	intron-variant	TOLLIP	GRCh38.p7	11:1305980	ACCCCTGTGAGGAGT[A/G]TCATGGGGGCCCCTG	54472
rs5743874	snp	C/T	0.0930568	0.194599	intron-variant	TOLLIP	GRCh38.p7	11:1305954	CCCTGCGAGGGGTAC[C/T]GTGCGGGCCCCCGCG	54472
rs5743875	snp	A/G/T	0.0215028	0.101435	intron-variant	TOLLIP	GRCh38.p7	11:1305939	CGTGCGGGCCCCCGC[A/G/T]AGGAGTATCGAGGAG	54472
rs5743876	snp	A/G	0.0126979	0.078662	intron-variant	TOLLIP	GRCh38.p7	11:1305919	GTATCGAGGAGTACC[A/G]TGTGGACCCCTGCCT	54472
rs5743877	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1305735	AGTCCAGCTGGAGGC[A/G]GCCTGGCCCCTCCCT	54472
rs5743878	snp	C/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1305698	CTGAGAGGCCTGTTC[C/G]TGTCCAGGTCCCCTC	54472
rs5743879	snp	A/G	0.0912534	0.193131	intron-variant	TOLLIP	GRCh38.p7	11:1305596	CTTTATCACTTCTTC[A/G]GTGTTTATTAACTGG	54472
rs5743880	snp	C/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1305547	GCTTTCCCCATCAAC[C/T]GGTGTCGGCTGGCTG	54472
rs5743881	snp	C/T	0.131723	0.220251	intron-variant	TOLLIP	GRCh38.p7	11:1305516	TCCTGAAACACAATT[C/T]GTGAAAGAAAGGCAA	54472
rs5743882	snp	C/T	0.00438332	0.0466095	intron-variant	TOLLIP	GRCh38.p7	11:1305475	TTTCCCTCATCTTCC[C/T]GTACCTCAAGGAGAG	54472
rs5743883	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305317	CTGCTCCTGGGAGGG[C/T]GTCCGTTCCTGCNGA	54472
rs5743884	snp	C/T	0.0252325	0.109451	intron-variant	TOLLIP	GRCh38.p7	11:1305304	GGCGTCCGTTCCTGC[C/T]GACTGCACCTGAGCC	54472
rs5743885	snp	C/T	0.334412	0.235318	intron-variant	TOLLIP	GRCh38.p7	11:1305068	TACTGGCATGGCCAC[C/T]CCAGCTGTCTTTTAG	54472
rs5743886	snp	A/G	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1304984	TTTTGTTTAAGACAC[A/G]TGCACCATCGATAGC	54472
rs5743887	snp	A/G	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1304909	TTTTGATGGGAATGC[A/G]CTAGTTTCATCTTTC	54472
rs5743888	snp	A/G	0.0252325	0.109451	intron-variant	TOLLIP	GRCh38.p7	11:1304815	TTTTATTTGTCCTAC[A/G]TTTTCTTATTTTTTT	54472
rs5743889	snp	G/T	0.0228947	0.104514	intron-variant	TOLLIP	GRCh38.p7	11:1304802	ACNTTTTCTTATTTT[G/T]TTTCTCTCATTGCCT	54472
rs5743890	snp	A/G	0.0912534	0.193131	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304599	AATAAATAAAGAAGA[A/G]GTTAATCATTGTCTG	54472
rs5743891	snp	A/G	0.101301	0.200969	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304158	GCTGCTGAGCAGCCC[A/G]GGAGTGGATGTCCCT	54472
rs5743892	snp	A/C	0.0955749	0.196603	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304103	GCCCTCTGTTTGCTG[A/C]CTTCTGAATACGCTG	54472
rs5743893	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303810	ggtctcaagtgatcc[A/G]cccacctcagcctcc	54472
rs5743894	snp	A/G	0.138207	0.223612	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303542	GCCCTGTTTCTTTGC[A/G]CAGCGCCTCCTGCCG	54472
rs5743895	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303292	TGACTGGCTTTTGTT[C/T]CATCTGAATGAGAAG	54472
rs5743896	snp	C/G	0.0588605	0.161139	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303195	TTCCTGGCAGAGACC[C/G]CATTTAAAGTCGCTT	54472
rs5743897	snp	A/C	0.127599	0.217986	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302839	GGGCTGCTGAGCGGC[A/C]GTGGGAGGAGGATGT	54472
rs5743898	snp	C/T	0.0952156	0.196321	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302514	CAGCAGCTGAGTGGG[C/T]ATGGGGAATTGCAGT	54472
rs5743899	snp	A/G	0.44858	0.151875	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302334	TCTCTGAAACCCTGC[A/G]CACTGAGGGGTCAGT	54472
rs5743900	snp	C/G	0.127944	0.218179	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302054	CAAGGCAGGGCCAGC[C/G]CCTCAGACACAGCAG	54472
rs5743901	snp	C/T	0.332568	0.235971	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301982	CTGGACCAACTGTGC[C/T]GTTCTATGTGAGTCC	54472
rs5743902	snp	A/G	0.484561	0.0864924	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301981	TGGACCAACTGTGCT[A/G]TTCTATGTGAGTCCT	54472
rs5743903	snp	C/T	0.0352966	0.128072	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301806	CCTTTAGCCACGAGC[C/T]CAGCCCAGGTCTTCC	54472
rs5743904	snp	A/G	0.334871	0.235153	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301568	GAGGAAACTTCTGGG[A/G]TTTGGCGGCCGTGTG	54472
rs5743905	snp	C/G	0.0912534	0.193131	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301483	GGGTTTTCTGGGTGT[C/G]CCAGCACATGGATAC	54472
rs5743906	snp	A/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301458	GGATACGGAGTTCTC[A/G]GAAGCCCGCGACACA	54472
rs5743907	snp	C/T	0.334871	0.235153	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301391	GGGTGGGCAGGCGCC[C/T]GCGGATGCCGTTTGT	54472
rs5743908	snp	C/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301355	atcctcagtgctggt[C/G]tgagactctggcttg	54472
rs5743909	snp	A/C	0.333491	0.235646	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300805	GGCCAGCCGTGCTTC[A/C]GGGGCGACTGTGGTG	54472
rs5743910	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300763	GGTGATGTCTCCTGG[A/C]AGGCGTGAGGCCAGG	54472
rs5743911	snp	A/G	0.495745	0.0459295	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300719	AGGACTCCACGTCCT[A/G]GGCTGAGCTGGGCTC	54472
rs5743912	snp	A/G	0.0681886	0.171594	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300639	CTCTCAGTCGGAAAC[A/G]TATTCCTAACAGGTG	54472
rs5743913	snp	A/C	0.0490535	0.14873	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300456	ATTAAGACTTTATTT[A/C]TGTGCCAAAACTAAA	54472
rs5743914	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300379	GACCTCTTTTCTTTC[A/G]TGTGGAAAGGTANGC	54472
rs5743915	snp	C/T	0.489083	0.0730708	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300366	TCGTGTGGAAAGGTA[C/T]GCTGCAGTGGTTTAG	54472
rs5743916	snp	G/T	0.0228947	0.104514	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300145	CTCTGTGGGATGAGA[G/T]CCCTACCCTGTCCTT	54472
rs5743917	snp	C/T	0.0861826	0.188849	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300109	TTTAAAAGTAATTCA[C/T]GAATGTTTTTAAAAA	54472
rs5743918	snp	A/G	0.0785177	0.181917	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300108	TTAAAAGTAATTCAC[A/G]AATGTTTTTAAAAAG	54472
rs5743919	snp	A/G	0.107694	0.205546	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299900	AGTCTCCATGTGTTC[A/G]CGGCAGGGACCGCCG	54472
rs5743920	snp	C/T	0.127599	0.217986	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299868	CTCCTGGTGAGGCCG[C/T]GTGGCGATGCGCTGG	54472
rs5743921	snp	A/G	0.0345262	0.126772	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299719	TGTTGGCCTTCACAC[A/G]GGCATTTAGACTTGT	54472
rs5743922	snp	A/G	0.0588605	0.161139	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299442	TCACTGAAACGATAG[A/G]GTTTACTTCAGCACC	54472
rs5743923	snp	C/G	0.127599	0.217986	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299264	CAGTATTTGTACGGG[C/G]AGGACTGAAGCCTGG	54472
rs5743924	snp	A/G	0.0912534	0.193131	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299043	GCTGGGGGCATGACT[A/G]TTGGCTCCAGGTTTT	54472
rs5743925	snp	A/C	0.00119737	0.0244387	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298599	AAATGACACTTGATC[A/C]TTAGGCCTTTGGATA	54472
rs5743926	snp	A/G	0.021333	0.101051	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298511	AGTGCAGAGCAAGGA[A/G]ATGGAGCGCTGGACG	54472
rs5743927	snp	C/G	0.0228947	0.104514	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298286	CTGTCTGTCCCCTAC[C/G]TGTGCCCAGGAGGGC	54472
rs5743928	snp	A/G	0.00597247	0.0543191	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298263	AGGAGGGCACGAGCC[A/G]CCTGTCTGTCTGCCA	54472
rs5743929	snp	C/G	0.00953873	0.0683987	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298128	TGTTAGTCCTGAGAA[C/G]TTGGTTAGCACGAGT	54472
rs5743930	snp	A/G	0.0341408	0.126114	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297818	GTTGAGCTGTACAGC[A/G]CCTCGAGAGAGGCTG	54472
rs5743931	snp	A/G	0.137187	0.223099	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297665	CGGAGGTGAAGCCGG[A/G]GTGCTCTGCTTGTTC	54472
rs5743932	snp	C/T	0.0232847	0.105357	intron-variant	TOLLIP	GRCh38.p7	11:1296450	GCCGCTGCAGGTGTG[C/T]GGGTGGTTTCGGGAT	54472
rs5743933	snp	A/G	0.0678174	0.1712	intron-variant	TOLLIP	GRCh38.p7	11:1296109	GGGCACACATGGTGC[A/G]AGGGAGACCCTTTAA	54472
rs5743934	snp	C/T	0.0908922	0.192833	intron-variant	TOLLIP	GRCh38.p7	11:1295327	GGCAGCTGGAGGAGG[C/T]GCGGCCGGCACCCCC	54472
rs5743935	snp	C/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1295228	CCACAGAGCAGCCCT[C/T]GGTCAGCCTCGGGGC	54472
rs5743936	snp	C/T	0.387074	0.209071	intron-variant	TOLLIP	GRCh38.p7	11:1295201	GGGCCGGCCCGTGGT[C/T]GCTTAGTGGTCTTTC	54472
rs5743937	snp	C/T	0.441432	0.160792	intron-variant	TOLLIP	GRCh38.p7	11:1295157	AATCGGCAGATTGAA[C/T]GCCGATTTTGATCAC	54472
rs5743938	snp	C/T	0.0368353	0.130617	intron-variant	TOLLIP	GRCh38.p7	11:1293797	TCACCCGTCCTCAGC[C/T]GCCACCTCCTGGCAG	54472
rs5743939	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1293519	CTCTTGGCTTCTGGG[C/T]GGCCACACAGGTGGT	54472
rs5743940	snp	A/G	0.0271762	0.113356	intron-variant	TOLLIP	GRCh38.p7	11:1293243	CTCCGTGTGCCCAAG[A/G]TGGAGCTCTCGGGCC	54472
rs5743941	snp	C/T	0.0111196	0.0737302	intron-variant	TOLLIP	GRCh38.p7	11:1293189	TCCGCAGGTGGCTGC[C/T]CCACACTCTGGAAGC	54472
rs5743942	snp	C/T	0.475348	0.108251	intron-variant	TOLLIP	GRCh38.p7	11:1292798	CGCCGTCTGCTGCGC[C/T]GTGTGTCTGCCGCGC	54472
rs5743943	snp	C/G	0.0248432	0.108648	intron-variant	TOLLIP	GRCh38.p7	11:1292698	TCTCTTGCCCGTTGT[C/G]GGGGAGGCAGCGGTG	54472
rs5743944	snp	A/G	0.252421	0.249988	intron-variant	TOLLIP	GRCh38.p7	11:1292679	GAGGCAGCGGTGCCC[A/G]TGTGTCCCCACGGTG	54472
rs5743945	snp	A/G	0.0210502	0.100409	intron-variant	TOLLIP	GRCh38.p7	11:1292588	GATGCTTCCATAAAC[A/G]TNGAGGAGGTCACTT	54472
rs5743946	snp	C/T	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1292586	TGCTTCCATAAACNT[C/T]GAGGAGGTCACTTCA	54472
rs5743947	snp	A/G	0.182296	0.240658	intron-variant	TOLLIP	GRCh38.p7	11:1292434	ATGTGAGCAGGCATC[A/G]GTGACAGGCACGGGC	54472
rs5743948	snp	A/G	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1292407	GGGCATGCTGGCAGG[A/G]GAGTCCCATGTGCCA	54472
rs5743949	snp	C/T	0.0912534	0.193131	intron-variant	TOLLIP	GRCh38.p7	11:1292398	GGCAGGGGAGTCCCA[C/T]GTGCCACCCAGAAAG	54472
rs5743950	snp	A/C/T	0.00319098	0.0398384	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290892	GGAGGAAAGCAGCCA[A/C/T]GTGGNGTCTGAATTA	54472
rs5743951	snp	C/T	0.0912534	0.193131	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290887	AAAGCAGCCACGTGG[C/T]GTCTGAATTATGTGC	54472
rs5743952	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290684	ATGGTGGGTGAGTGG[C/T]GGCCTCAGCTGTGTC	54472
rs5743953	snp	C/T	0.00826041	0.0637336	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290202	ACGTGCCAGCTATTA[C/T]GGAGGCTGCACGTGG	54472
rs5743954	snp	A/G	0.0121054	0.0768516	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290180	TGCACGTGGCTGAGC[A/G]TGGCTGCCGTGGGGA	54472
rs5743955	snp	A/C	0.0460142	0.144533	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289967	CAGCGTGCACGTGTC[A/C]CCTCCGCTGGGCGCA	54472
rs5743956	snp	A/G	0.0364509	0.129988	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289888	GCACGTGTCCCCTCC[A/G]CTGGGCACTGATCTG	54472
rs5743957	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289798	GGCACTCGTCTGGCC[A/G]CTCACCAGCAGGTGG	54472
rs5743958	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289627	TTTCCAGGGACAGAG[C/T]GTGCATGTGTCCGCC	54472
rs5743959	snp	C/T	0.182296	0.240658	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289603	GTCCGCCCCGCTGGG[C/T]GCACAGGGTCCGGCC	54472
rs5743960	snp	C/T	0.0581099	0.160244	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289588	CGCACAGGGTCCGGC[C/T]GCTCACCAGCAGGTG	54472
rs5743961	snp	A/G	0.0919752	0.193722	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289484	AGGGTCCTGAGTCCC[A/G]TCCGTGGCTGCACCT	54472
rs5743962	snp	G/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289392	TGGTCCTGGCACCTC[G/T]CACCTGTGGCATTGT	54472
rs5743963	snp	A/G	0.18325	0.240924	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289351	ACTGGGTGGGGGCCG[A/G]GGAGCAGTGTGGGGC	54472
rs5743964	snp	C/T	0.0912534	0.193131	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289312	CAGCAGACGGCCAGC[C/T]CTCCCTGCCTGGGCC	54472
rs5743965	snp	C/T	0.0898077	0.191933	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289309	CAGACGGCCAGCCCT[C/T]CCTGCCTGGGCCCTG	54472
rs5743966	snp	C/T	0.0908922	0.192833	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289039	GCAGCCCAGGGCCCT[C/T]GCTTTCCCCAGCCCC	54472
rs5743967	snp	C/T	0.0126979	0.078662	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288934	CGATCGTGAAGCCTG[C/T]GCTGCCCGAGGGGTC	54472
rs5743968	snp	C/T	0.0209421	0.100162	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288914	CCCGAGGGGTCTCAT[C/T]GATGGGGTGTTGGTG	54472
rs5743969	snp	C/T	0.00318214	0.0397611	intron-variant	TOLLIP	GRCh38.p7	11:1288781	CTCCCTCTTGTCTCC[C/T]GCAGAGAGCCTTCTC	54472
rs5743970	snp	A/G	0.109108	0.206518	intron-variant	TOLLIP	GRCh38.p7	11:1288553	GGGCTATGCCGCCCC[A/G]CAGACACCCTTGTCT	54472
rs5743971	snp	C/T	0.0210502	0.100409	intron-variant	TOLLIP	GRCh38.p7	11:1288545	CCGCCCCNCAGACAC[C/T]CTTGTCTCTTTCCTG	54472
rs5743972	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1288325	GGCCCCTGTGTCCTC[A/G]GAGGACCCCCACAGC	54472
rs5743973	snp	A/C	0.111576	0.20818	intron-variant	TOLLIP	GRCh38.p7	11:1288217	CCAGGCTCCTCCCCA[A/C]AGGGCAGGCATTGGC	54472
rs5743974	snp	C/T	0.0142736	0.0832652	intron-variant	TOLLIP	GRCh38.p7	11:1288201	AGGGCAGGCATTGGC[C/T]GTGGTGTGGCAGGGC	54472
rs5743975	snp	C/T	0.0215028	0.101435	intron-variant	TOLLIP	GRCh38.p7	11:1288109	TGGCTGTGGGGCCAG[C/T]ACGTCAGCGCCCTGG	54472
rs5743976	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1286258	GGAGCAGGGCCCAGC[A/G]TCCCCTGTGCACTCA	54472
rs5743977	snp	C/T	0.000368019	0.01356	intron-variant	TOLLIP	GRCh38.p7	11:1286105	CCCCGGGACCATCTC[C/T]GCTGTGTTTCAGCTG	54472
rs5743978	snp	C/T	0.0894459	0.191631	intron-variant	TOLLIP	GRCh38.p7	11:1285892	GGTGGGGACGTCATC[C/T]ATTCTAGAATCCTGT	54472
rs5743979	snp	C/T	0.00636936	0.0560724	intron-variant	TOLLIP	GRCh38.p7	11:1285656	CCCTGTCAGGTGACA[C/T]GTGCTCTGCACTGTG	54472
rs5743980	snp	C/T	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1285591	GCGTGCCCTGCGCTG[C/T]GCCGTTGTGTCTGAA	54472
rs5743981	snp	A/C	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1285571	TTGTGTCTGAACCTC[A/C]CGCTCCTGTTGGGTG	54472
rs5743982	snp	C/T	0.0248432	0.108648	intron-variant	TOLLIP	GRCh38.p7	11:1285401	CTGCTGGTGCAAGAC[C/T]GGCCCCCACCATGGA	54472
rs5743983	snp	A/G	0.084364	0.187256	intron-variant	TOLLIP	GRCh38.p7	11:1285280	GAGGTGGCCTCTCTC[A/G]TTCTGGGGAGCTGGT	54472
rs5743984	snp	A/G	0.0883596	0.190715	intron-variant	TOLLIP	GRCh38.p7	11:1285054	GAGCTGCTGGCAGGC[A/G]AGAGTGCTGTGAGGC	54472
rs5743985	in-del	-/GAG	0.0966517	0.197444	intron-variant	TOLLIP	GRCh38.p7	11:1284877	GACGATGGGAAGGAG[-/GAG]ACGGCACTGGGAGAC	54472
rs5743986	snp	C/T	0.0225045	0.103662	intron-variant	TOLLIP	GRCh38.p7	11:1284656	GTCTTAGAAAACCAC[C/T]AGCCTGGGGGTGGGT	54472
rs5743987	snp	A/G	0.147656	0.228091	intron-variant	TOLLIP	GRCh38.p7	11:1284616	CATGCCTCTAATCCC[A/G]GCACCTTGGGAGGCC	54472
rs5743988	snp	A/G	0.0279526	0.114869	intron-variant	TOLLIP	GRCh38.p7	11:1284509	ACAAACAAATTAGCC[A/G]GGCGCGGTGGTGGGC	54472
rs5743989	snp	A/G	0.0368353	0.130617	intron-variant	TOLLIP	GRCh38.p7	11:1284409	gtgagccgagattgc[A/G]ccactgcactccagc	54472
rs5743990	snp	A/G	0.0210502	0.100409	intron-variant	TOLLIP	GRCh38.p7	11:1284071	CCCAGAGTGGCTCCT[A/G]GAGGTTCTGATTTGT	54472
rs5743992	snp	C/T	0.0919752	0.193722	intron-variant	TOLLIP	GRCh38.p7	11:1283444	TCCAATAAGCAGGGG[C/T]GTCCCTGGCACAGTA	54472
rs5743993	snp	A/G	0.0368353	0.130617	intron-variant	TOLLIP	GRCh38.p7	11:1283110	TGGTGTGACTTGCTC[A/G]TCCCTCACGGCGGGC	54472
rs5743994	snp	C/T	0.0422008	0.138995	intron-variant	TOLLIP	GRCh38.p7	11:1282865	ATCCATGTGCCATGT[C/T]GGTGTGCTGCACCCA	54472
rs5743995	snp	A/G	0.0244538	0.107838	intron-variant	TOLLIP	GRCh38.p7	11:1282730	gtgcaggtttgttac[A/G]tatgtatccgtgtgc	54472
rs5743996	snp	A/T	0.0209421	0.100162	intron-variant	TOLLIP	GRCh38.p7	11:1281508	GGGCTCACTGTGCAC[A/T]TTAGGTGGGCTCAGG	54472
rs5743997	snp	A/G	0.0221141	0.102801	intron-variant	TOLLIP	GRCh38.p7	11:1281067	AGGAAACATCTAGGC[A/G]TGAAGCATCTGGAGA	54472
rs5743998	snp	A/G	0.0368353	0.130617	intron-variant	TOLLIP	GRCh38.p7	11:1281047	GCATCTGGAGACCGC[A/G]TGGCCTCATGAAGCA	54472
rs5743999	snp	C/T	0.00874735	0.0655527	intron-variant	TOLLIP	GRCh38.p7	11:1280753	CTCTGGGGCCCTCCT[C/T]ACTTTCCCTCCTCCT	54472
rs5744000	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1280557	TTCCCTCGTGCACCT[C/G]CATTTCACACGGGCC	54472
rs5744001	snp	C/T	0.00874735	0.0655527	intron-variant	TOLLIP	GRCh38.p7	11:1280477	GTCCCTCCCGTCATC[C/T]TGGCCTGCGTCTCTG	54472
rs5744002	snp	A/G	0.497445	0.0356514	intron-variant	TOLLIP	GRCh38.p7	11:1280458	CCTGCGTCTCTGTGG[A/G]CACAACCCCCACTGG	54472
rs5744003	snp	C/T	0.0894459	0.191631	intron-variant	TOLLIP	GRCh38.p7	11:1279564	CCGCCCATCACTCCT[C/T]CCAGGGCCGCTACAG	54472
rs5744004	snp	C/T	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1279556	CACTCCTNCCAGGGC[C/T]GCTACAGGTGGGCTC	54472
rs5744005	snp	C/T	0.00557542	0.0525036	intron-variant	TOLLIP	GRCh38.p7	11:1279463	CAGGCCCCAGAGCTC[C/T]TGGTCTGTCCTCCTG	54472
rs5744006	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1279286	CCCCTCAGCCCACAC[C/T]GTGGAAGCACCCACC	54472
rs5744007	snp	C/T	0.0193772	0.0965046	intron-variant	TOLLIP	GRCh38.p7	11:1278764	CACCTGGCCATGGTT[C/T]GGTTCGTTTTCCGTC	54472
rs5744008	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1278651	GGGTGTGGAGGAAAG[A/G]TGGGCCTGGCCCTGA	54472
rs5744009	snp	C/G	0.0209421	0.100162	intron-variant	TOLLIP	GRCh38.p7	11:1278527	GAGTCCTGGCCTTTG[C/G]AGCAGGTGCAGGAGG	54472
rs5744010	snp	C/T	0.0210502	0.100409	intron-variant	TOLLIP	GRCh38.p7	11:1278499	AGGCTTGGTGGCAAG[C/T]CCTGTCTGCTCCGTT	54472
rs5744011	snp	A/G	0.0244538	0.107838	intron-variant	TOLLIP	GRCh38.p7	11:1278453	CTTGTTGCTGGTGTT[A/G]GTTCAGGCCAGGATT	54472
rs5744012	snp	G/T	0.00874735	0.0655527	intron-variant	TOLLIP	GRCh38.p7	11:1278161	CCTGTGCTCAGGGCT[G/T]CTCGTGGTTTTAGGG	54472
rs5744013	snp	A/G	0.0898077	0.191933	intron-variant	TOLLIP	GRCh38.p7	11:1277735	AAAGCATCTTCTAGA[A/G]TGCCTGATAAAGGAA	54472
rs5744014	snp	C/G	0.0905309	0.192535	intron-variant	TOLLIP	GRCh38.p7	11:1277309	CTTCAGCAGGAGCTA[C/G]TGTGGCACTTCTGGA	54472
rs5744015	snp	G/T	0.0789902	0.182367	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277200	GCCCTGCCCCCGGCC[G/T]CCGTGAACGCCCAGC	54472
rs5744016	snp	C/T	0.0013547	0.0259907	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277135	GGACATGTTCCCCAA[C/T]ATGGACCAGGAGGTG	54472
rs5744017	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276986	GACACGCCGACCCGG[C/T]GCTCCCCAAGGAATG	54472
rs5744018	snp	G/T	0.0144158	0.0836666	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276845	GCGGTCCAGGACGGG[G/T]CGGGGGCTCCCCTCC	54472
rs5744019	snp	G/T	0.000284374	0.0119208	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276744	CTGGAAAATGCTCTT[G/T]CTGTAGAGAGCAGCT	54472
rs5744020	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276343	CTGATTGCCAGCCAG[C/T]GGGCNTCTGAAGCCG	54472
rs5744021	snp	A/G	0.0210502	0.100409	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276338	TGCCAGCCAGNGGGC[A/G]TCTGAAGCCGGGTCC	54472
rs5744022	snp	C/T	0.0210502	0.100409	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276127	TTGGGAGCTGCTGTG[C/T]CCAGNANGTGGGTTC	54472
rs5744023	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276122	AGCTGCTGTGCCCAG[A/G]ACGTGGGTTCAGCGT	54472
rs5744024	snp	C/T	0.0970103	0.197722	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276120	CTGCTGTGCCCAGGA[C/T]GTGGGTTCAGCGTGG	54472
rs5744025	snp	A/G	0.0142736	0.0832652	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276105	CGTGGGTTCAGCGTG[A/G]GCGAGGAAAGCCTGG	54472
rs5744026	snp	C/T	0.021333	0.101051	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276089	GCGAGGAAAGCCTGG[C/T]GAGCGTGGCCCTGTA	54472
rs5744027	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276058	AAAGCTTTCTGAGGC[A/G]GGAGGCNCTCACTTA	54472
rs5744028	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276051	TCTGAGGCGGGAGGC[A/G]CTCACTTACCTCTGA	54472
rs5744029	snp	A/G	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275941	AGAAGCTTCTCACAA[A/G]TGATGCACTTTAAAT	54472
rs5744030	snp	C/T	0.0225045	0.103662	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275521	TATTTGTTCAGCAGA[C/T]GCCGACCACTCAGAC	54472
rs5744031	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275388	TAGATGGTATGTTCC[A/G]TGATATTAACAACTC	54472
rs5744032	snp	A/C	0.093777	0.195178	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275133	CACACAGTGGGGGCC[A/C]GCCTCGCTGGAGGGA	54472
rs5744033	snp	C/G	0.134802	0.221877	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275033	TTTTAATAGACAAAT[C/G]ACATTTTGCAAGGCC	54472
rs5744034	snp	C/T	0.134802	0.221877	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275007	AGGCCTTTAATTAAA[C/T]AAGATTCTTCTTTCC	54472
rs5744035	snp	A/C	0.0201999	0.0984476	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274832	TGGATGAGGTCGTCA[A/C]ACTCAGAAGGACAGG	54472
rs5744036	snp	A/G	0.277778	0.248452	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274596	AGAAGACAGGTCGCC[A/G]GAGGCTCCCCCTCCT	54472
rs5744037	snp	A/G	0.0916144	0.193427	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274366	GGGAAGGTTTACCAT[A/G]TTTGTTCCCGAGTAT	54472
rs5744038	snp	A/G	0.153332	0.230554	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274206	GAGGAGGGAAGTCCC[A/G]GGTGCTCCTCCCTCA	54472
rs5744039	snp	A/C	0.0337553	0.125452	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274104	CTTTTCATTTCCAGG[A/C]CATTTCCATCTGGGA	54472
rs6578971	snp	A/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287394	GCAGCTCCCTGCTGC[A/T]GCCTCCCCGCCGCAG	54472
rs7105761	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287465	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs7105782	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287535	AGCCTCCCCGCCGCA[C/G]CCTCACCGCCGCAGC	54472
rs7107064	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305419	TCTTCACAACACTCA[A/G]GGGAGAGAAAGCCCA	54472
rs7108920	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287479	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs7108928	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287493	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs7481348	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294235	CCTTTCCCTGCATTT[C/T]TACGAAAGCCCGCGT	54472
rs10839956	snp	C/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1279685	TCACGTTCTTCACGC[C/T]GTGTGAATCTGCTGT	54472
rs10840239	snp	A/G	0.461481	0.133325	intron-variant	TOLLIP	GRCh38.p7	11:1294352	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs10909565	snp	A/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294631	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs11041743	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1280987	CTGCTGTTGCCAGCC[C/T]GGCGGAGAGTCTCTG	54472
rs11042045	snp	C/T	0.123798	0.215808	intron-variant	TOLLIP	GRCh38.p7	11:1287015	CGAAACTGTCAGCTG[C/T]GGATAAGTCACTGCA	54472
rs11042249	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292478	CTTCTGCCACACTCA[A/G]CGTCATCCTCTCATT	54472
rs11042368	snp	A/G	0.277778	0.248452	intron-variant	TOLLIP	GRCh38.p7	11:1294537	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs11042394	snp	C/G	0.277778	0.248452	intron-variant	TOLLIP	GRCh38.p7	11:1294903	TTCTACGAAAGCCCG[C/G]GTGGCTCACAGTGTG	54472
rs11042484	snp	A/G	0.127254	0.217792	intron-variant	TOLLIP	GRCh38.p7	11:1297082	GGGGCCCCGGTCAGC[A/G]CCAGTGCCCTGGGCA	54472
rs11042542	snp	A/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299007	caggggacagtcatc[A/G]aaaaaccaggacagc	54472
rs11042781	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303935	cagctactcgggagt[C/T]tgaggcaggaaaatc	54472
rs11042783	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303950	ctgaggcaggaaaat[C/T]gcttgaacctgggag	54472
rs11043006	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308848	GCCCGCCTCCACCTG[G/T]GGGGCCATCAGGGTG	54472
rs11607136	snp	A/G	0	0	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274292	TCCCAGTCTGTTGAC[A/G]AGTGAACTCTGATTC	54472
rs11608022	snp	A/C	0.24449	0.249939	intron-variant	TOLLIP	GRCh38.p7	11:1287820	CCCCGCCGCAGCCTC[A/C]CCGCCGCACCCTCCC	54472
rs12278738	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1286199	CGCCAGCCCAGAATC[A/G]CCCTCCCCATGCCAG	54472
rs12279847	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299006	gcaggggacagtcat[C/T]gaaaaaccaggacag	54472
rs12280761	snp	C/T	0.324855	0.23853	intron-variant	TOLLIP	GRCh38.p7	11:1291965	TCTGTTTTCTATTCT[C/T]GTCCACATACAAGTT	54472
rs12290986	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303822	gggcggatcacttga[A/G]accaggagttcgaga	54472
rs12294518	snp	C/T	0.0912534	0.193131	intron-variant	TOLLIP	GRCh38.p7	11:1292185	TGCTGCACACCCACA[C/T]ATCTGCTAGATCAGC	54472
rs12365946	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1292253	CAACTGCCCTATTTT[C/T]TGGAGAGTATGTAGC	54472
rs12421317	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1306627	GGGTAAAGGCCCACT[A/G]TGGGTTAATTCAGAG	54472
rs12785349	snp	C/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294786	CGGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA	54472
rs12788138	snp	C/T	0	0	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309750	CCTCTCGCCCGGCGC[C/T]TGCGCACCTGCTCTC	54472
rs12789854	snp	A/G	0.492337	0.0614248	intron-variant	TOLLIP	GRCh38.p7	11:1294960	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs12793865	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294572	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG	54472
rs12793909	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294619	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG	54472
rs12793917	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294638	TGGCTCACGGTGTGT[C/T]TCCTTTCCCTGCATT	54472
rs12795602	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1281073	GATGCTTCACGCCTA[A/G]ATGTTTCCTTAAAAT	54472
rs12796761	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308915	CGGGGCCCGCCTCCA[C/T]CTAGGGTGCCATCAG	54472
rs12800885	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308904	CCATCAGGGTGCGGG[A/G]CCCGCCTCCATCTAG	54472
rs12800914	snp	C/T	0.291493	0.246533	intron-variant	TOLLIP	GRCh38.p7	11:1291707	CCGCCCCGTCCTCGC[C/T]GACCCCCCTCTGAGG	54472
rs12800917	snp	G/T	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308957	CGCCTCCACCTGGGG[G/T]GCCATCAGGGAGCAG	54472
rs12805480	snp	A/C	0.277778	0.248452	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308857	CACCTGGGGGGCCAT[A/C]AGGGTGCGGGACCCG	54472
rs12805687	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308950	CGGGACCCGCCTCCA[C/T]CTGGGGGGCCATCAG	54472
rs12808025	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308939	CCATCAGGGTGCGGG[A/G]CCCGCCTCCACCTGG	54472
rs28470184	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1296837	GTGGAGGCCTGGTTG[A/C]TGGTGGAGTGGGGTG	54472
rs28513839	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1296841	AGGCCTGGTTGCTGG[A/T]GGAGTGGGGTGGAGG	54472
rs34259532	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276869	GACCGCCAGGAACCG[-/A]AAAACCCACATGCAC	54472
rs34437291	in-del	-/AG	0.0839998	0.186933	intron-variant	TOLLIP	GRCh38.p7	11:1285668	CACGTGTCACCTGAC[-/AG]GGGCGTGAGGTTCTC	54472
rs34500638	in-del	-/A			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299819	GTCACCTGTGCCGTC[-/A]AAAACGCCCCATCCA	54472
rs34569007	in-del	-/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301675	ACAAAGCCAGCCCAC[-/G]GGAGGCCCCAACACA	54472
rs34589655	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1288287	GGCTGCTCAGCTGGA[-/C]CCTAAGGGCAGAGCT	54472
rs34703157	in-del	-/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290112	AATGAAACACCAGGT[-/G]GGGGAGCCACGCCTC	54472
rs34787245	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289602	CGGCCGGACCCTGTG[C/T]GCCCAGCGGGGCGGA	54472
rs34793197	in-del	-/A			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304762	ACAACTGAATTTTTT[-/A]AAAACTCCATTTAAT	54472
rs35045124	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276388	CCGTGCCAGGCCCCC[-/T]TTCCTCACTCCAGGT	54472
rs35194940	in-del	-/G			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299243	AGCAAGAGAGGAGAC[-/G]GGAGACCAGGCTTCA	54472
rs35279068	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1285519	CCTAACAGTGACACA[C/T]GACAACAGACGCAAC	54472
rs35290340	in-del	-/T			intron-variant	TOLLIP	GRCh38.p7	11:1292645	CACATGCTGTTCTGG[-/T]TGCAGGAGACACTGT	54472
rs35307059	in-del	-/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273945	GTGCCAGGGTGGCTC[-/G]GGGGTCTCTAGAGTG	54472
rs35365323	snp	C/T	0.0363512	0.129824	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277097	TCCTTGTTCCCTCGC[C/T]GGGCTTCCAGCACGG	54472
rs35395733	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1294622	TCTACGAAAGCCCGC[A/G]TGGCTCACAGTGTGT	54472
rs35446898	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1294899	GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG	54472
rs35483730	in-del	-/G			intron-variant	TOLLIP	GRCh38.p7	11:1293453	CCTTGGCATCCCACT[-/G]GGGGCCCCAGGAGAC	54472
rs35534043	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275249	CACGCGTGTGGCAGT[-/C]CTCACTGCACCCCAG	54472
rs35599839	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1283160	ACCTGCGCTGGGTGG[-/A]ATCTGCGGTGGTGGC	54472
rs35650910	in-del	-/C			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299825	TGTGCCGTCAAAACG[-/C]CCCCATCCACCAGCC	54472
rs35743811	snp	A/G	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1287164	GAAACTGTCAACTGC[A/G]GATAAGTCACTGCAC	54472
rs35791007	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287822	CCGCCGCACCCTCCC[C/T]GCCGCACCCTCCCTG	54472
rs41307082	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277478	GGGCCCTCTGTGACG[C/T]CTCCTTCACTAACTC	54472
rs41310328	snp	C/T	0.0182019	0.0936463	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275127	TTGCTCTCCCTCCAG[C/T]GAGGCTGGCCCCCAC	54472
rs41314515	snp	C/T	0.0166325	0.0896639	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276907	CAGGTGTGGACGGGG[C/T]GGCACAGAAGTCCAC	54472
rs41317292	snp	C/G	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276035	CGCAGCGCCCAGGCA[C/G]TCAGAGGTAAGTGAG	54472
rs41317294	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275679	ACAGTATATTTGACA[A/G]AAACCACCCCCAATC	54472
rs55646946	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294171	GCATGGCTCAGTGTG[C/T]CTCCTTTCCCTGCAT	54472
rs55647350	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275605	AGGCGCCTGCTGCCA[A/G]CATGTCCCTCCCCCA	54472
rs55660304	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308968	GGGGGGCCATCAGGG[A/T]GCAGGGCCCGCATCC	54472
rs55686144	snp	A/C/T	0.00159649	0.0282165	intron-variant	TOLLIP	GRCh38.p7	11:1291546	CCCCGAAGGCACGGC[A/C/T]ACCCCATCCTCACTG	54472
rs55686260	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287437	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs55764960	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291742	GGCCGCCCCGTCCTC[A/G]CCGACCCACCTCTGA	54472
rs55793034	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1294933	GTCTCCTTTCCCTGC[A/G]TTTCTACGAAAGCCC	54472
rs55809655	in-del	-/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308871	TCAGGGTGCGGGACC[-/C]GCCTCCACCTGGGGG	54472
rs55837816	snp	G/T	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309004	GGGGACCATTAGGGT[G/T]CAGGGCCCGCCTCCA	54472
rs55883441	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308922	CGCCTCCATCTAGGG[G/T]GCCATCAGGGTGCGG	54472
rs56000022	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308974	CCATCAGGGAGCAGG[A/G]CCCGCATCCATCTAG	54472
rs56038704	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287451	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs56128747	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1291545	CCCCCGAAGGCACGG[C/G]CACCCCATCCTCACT	54472
rs56156644	snp	C/T	0.0217236	0.101931	intron-variant	TOLLIP	GRCh38.p7	11:1292012	AATCAAAGCTGTGGC[C/T]GGTCCTTTTAGGTCA	54472
rs56178536	snp	A/C	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308980	GGGAGCAGGGCCCGC[A/C]TCCATCTAGGGGACC	54472
rs56199234	snp	A/G	0.0111196	0.0737302	intron-variant	TOLLIP	GRCh38.p7	11:1283818	AGCCACAGAGCGCCC[A/G]GCCCAGAAGTTGGAG	54472
rs56241462	in-del	-/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308864	GGGCCATCAGGGTGC[-/C]GGGACCCGCCTCCAC	54472
rs56362227	snp	A/C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291335	CTCCTGCAGCCAACC[A/C/T]GGCTCACCCCCAGGA	54472
rs56376537	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294277	TGTCTCCTTTCCCTG[C/T]ATTTCTACGAAAGCC	54472
rs56397575	snp	C/T	0.0217236	0.101931	intron-variant	TOLLIP	GRCh38.p7	11:1291755	TCACCGACCCACCTC[C/T]GAGGGCACGGCCGCC	54472
rs56733424	snp	A/G	0.277778	0.248452	intron-variant	TOLLIP	GRCh38.p7	11:1295007	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs56933202	in-del	-/TT			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299532	TCCTAAAATTTATTT[-/TT]GCCATATGATGATGG	54472
rs57461270	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1294305	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs57827674	snp	C/T	0.0869089	0.189476	intron-variant	TOLLIP	GRCh38.p7	11:1282597	AACCTGCACGTTGTG[C/T]ACATGTACCCTAAAA	54472
rs58677632	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1283418	CAGTGTCAGCTTCAT[A/C]TAGATGGCCGTACTG	54472
rs60020941	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308918	GGCCCGCCTCCATCT[A/G]GGGTGCCATCAGGGT	54472
rs60404204	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1292089	GGCCACAGCGTACTC[C/T]GGAATGCTATGGAGT	54472
rs61869685	snp	C/T	0.471673	0.115589	intron-variant	TOLLIP	GRCh38.p7	11:1287388	AGAAAAGCAGCTCCC[C/T]GCTGCTGCCTCCCCG	54472
rs71025719	in-del	-/CCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCCGCA	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287800	ACCCTCCCCGCCGCA[lengthTooLong]GCCTCCCCGCCGCAC	54472
rs71025722	in-del	-/TGGGGCCATAAGGGTGCCGGGACCGCCTCCACCTG	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308847	GCCCGCCTCCACCTG[lengthTooLong]GGGGGCCATCAGGGT	54472
rs71454080	snp	C/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287696	CCGCCGCACCCTCCC[C/T]GCCGCACCCTCCCCG	54472
rs71454081	snp	C/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287815	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs71454082	snp	C/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287871	ACCCTCTCTGCTGCA[C/G]CCTCCCTGCTGCACC	54472
rs71454083	snp	A/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294678	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs71454084	snp	C/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294833	CAGTGTGTCTCCTTT[C/T]CCTGCATTTCTACGA	54472
rs71454085	snp	A/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294866	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs71454087	snp	A/G	0.277778	0.248452	intron-variant	TOLLIP	GRCh38.p7	11:1294913	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs71472142	multinucleotide-polymorphism	CA/TG	0	0	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301981	AGGACTCACATAGAA[CA/TG]GCACAGTTGGTCCAG	54472
rs72846381	snp	A/G	0.0268816	0.112775	intron-variant	TOLLIP	GRCh38.p7	11:1285998	AGGGAGGGAGCACAC[A/G]CACCTGTGATGGGCA	54472
rs72846383	snp	C/T	0.135143	0.222054	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291288	GTCCTGCCTGGAATG[C/T]AGACGGCCTCCCTGT	54472
rs72846392	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1306441	CAGGGTCTCCCGAGC[C/G]AGAGTCCTGCCCCCG	54472
rs73397883	snp	C/T	0.0588605	0.161139	intron-variant	TOLLIP	GRCh38.p7	11:1287999	GGTTGATGATACAGA[C/T]GAGACGGCAGGAGCT	54472
rs73397894	snp	A/G	0.0912534	0.193131	intron-variant	TOLLIP	GRCh38.p7	11:1297340	ACCCCGAGAGGGTCT[A/G]GCTCCTCACCTGTGT	54472
rs73399804	snp	A/G	0.0980852	0.198549	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310652	GGAACACCCTGCTCT[A/G]TGGAGTAGCCATTCT	54472
rs74046285	snp	C/T	0.0345262	0.126772	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300104	GAAACTTTTTAAAAA[C/T]ATTCGTGAATTACTT	54472
rs74046287	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310856	TGGTCAGTTCTCAGT[C/T]CTCGTCCTCCGGGAA	54472
rs74503040	snp	A/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294725	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs74577337	snp	A/G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298010	CTGGCCACACAGGAC[A/G/T]TGCTTCCCTGCCAAC	54472
rs74692168	snp	C/T	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287867	CCGCACCCTCTCTGC[C/T]GCAGCCTCCCTGCTG	54472
rs74860345	snp	A/G	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309041	GGACCATTAGGGTGC[A/G]GGGCCCTCCTCCATT	54472
rs74929271	snp	C/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1287423	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs75239657	snp	A/C	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1283307	AAGATGGGGACCCCT[A/C]CAGGCCAAGGGAGGC	54472
rs75406859	snp	A/C	4.97475e-05	0.00498711	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277055	TATGGCTCCTCCCCC[A/C]TCTGCAGCAGGGAGT	54472
rs75621936	snp	C/T	0.0379877	0.132479	intron-variant	TOLLIP	GRCh38.p7	11:1286242	CTCGCTACACGAGCC[C/T]TGAGTGCACAGGGGA	54472
rs75980902	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294340	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG	54472
rs76167907	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274511	TAATCAGAAGCGCAC[A/G]TTCTGAGACCACTCC	54472
rs76729597	snp	G/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1280227	TTCCACGTGCGAGGG[G/T]AAGCATGCCTGGGCC	54472
rs77124907	snp	A/G	0.0383715	0.133092	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311132	AAGCTATTAACCACA[A/G]GTTCCTGCTTTGGGG	54472
rs77169890	snp	A/C	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309015	GGGTTCAGGGCCCGC[A/C]TCCACCTGGGGGACC	54472
rs77240435	snp	G/T	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309039	GGGGACCATTAGGGT[G/T]CGGGGCCCTCCTCCA	54472
rs77443790	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310097	AGATGGGGCGCGGTT[C/T]CTCCACGGGGCGGCT	54472
rs77825895	snp	C/T	0.0275645	0.114116	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303677	AGGGACAGGAAACAC[C/T]TGCACAGCAGGCCTA	54472
rs78406765	snp	A/C			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299726	TAAATGCCCGTGTGA[A/C]GGCCAACAATTCCAC	54472
rs78468814	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310786	ATCAGGACCCTTTTC[C/T]GGTAACACAACCACT	54472
rs78488441	snp	C/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1278677	CACCCACACCTGCCT[C/T]TTGTCCTGGCCACTG	54472
rs78736015	snp	A/G	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309023	GGCCCGCCTCCACCT[A/G]GGGGACCATTAGGGT	54472
rs78992644	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1306104	ATGCAGACTATATTG[A/G]AAAAAGGTTATCTTT	54472
rs79145389	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1294343	TCTACGAAAGCCCGC[A/G]TGGCTCACGGTGTGT	54472
rs79364943	snp	A/C			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298573	CTCATTACTGGGAGA[A/C]AATAAAATTATATCC	54472
rs79892483	snp	A/G	0	0	intron-variant	TOLLIP	GRCh38.p7	11:1294584	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs79983698	snp	G/T	0	0	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309048	TAGGGTGCGGGGCCC[G/T]CCTCCATTCGGGAGT	54472
rs80293662	snp	A/C	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1285788	AAAAAAAAAAAAAAA[A/C]CAATTCTATTTTCTA	54472
rs80326424	snp	C/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1307017	CCCACCGGGCCGTCA[C/G]CACACAGCTCAGCTG	54472
rs111163740	snp	A/C	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1296809	GTGGAGGCCTGGTTG[A/C]TGGAGGAGTGGGGTG	54472
rs111277153	snp	A/C	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1286709	TAGTTCAAAACTGTC[A/C]ACTGTGGATAAGTCA	54472
rs111352533	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1286885	ATAAGTCACTGCACT[A/G]CTGTCTCCTGAGTTC	54472
rs111521887	snp	C/G	0.134802	0.221877	intron-variant	TOLLIP	GRCh38.p7	11:1291476	GAGGGAACGGCCAAC[C/G]TGTCCACACCAACCC	54472
rs111539110	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1288883	CGTCTTATCTGTGGA[A/G]CAGGGCTCCCACCTG	54472
rs111550675	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1297074	CGTCTGCAGGGGCCC[C/T]GGTCAGCGCCAGTGC	54472
rs111555946	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1296738	TGCTGGAGGAGTGGG[A/G]TGGAGGCCTGGTTGC	54472
rs111561835	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1293576	TGGCCCAGTGAGGAG[A/G]CAGGAATGTTTCCCA	54472
rs111590044	snp	C/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1287890	CCCTGCTGCACCCTC[C/T]CTGCTGCACCCTCTC	54472
rs111658007	snp	C/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1279967	TCCAGCTCAGAGACT[C/G]TTCCGGAACTCCCAA	54472
rs111777511	snp	A/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1294258	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs111831428	snp	A/G	0.000730922	0.0191031	intron-variant	TOLLIP	GRCh38.p7	11:1288595	AACATACCCCAATGC[A/G]CCCCACCCCGCCCAG	54472
rs111866843	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289305	AAGGCAGGGCCCAGG[A/C]AGGGAGGGCTGGCCG	54472
rs111971432	snp	C/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1279198	GGGATGTGGCGCCGA[C/G]TGGCCCTCAAGTGAA	54472
rs111986008	snp	C/T	0.0100364	0.0701248	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277074	GCAGCAGGGAGTTGA[C/T]GGCGGCATCCTTGTT	54472
rs111992209	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297999	CCGGGGGACACCTGG[A/C]CACACAGGACGTGCT	54472
rs112045310	snp	C/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1295405	GAGCCAGGCCCTACA[C/T]AGAGCAGACGCCCAC	54472
rs112070965	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289736	TGTGCGGCAAGACCC[C/T]GTGCGCCCAGCGGGG	54472
rs112084278	in-del	-/CAA	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1285789	AAAAAAAAAAAAAAA[-/CAA]TTCTATTTTCTAGAT	54472
rs112321894	snp	G/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1279853	CCGCCGGTGGGCAGG[G/T]GAGCATCAGCCCTGC	54472
rs112434701	snp	A/G	0	0	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298715	GAAGCAGCTCCCTGC[A/G]GATGGAGCTCATCAG	54472
rs112445940	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1296608	TGCTGGTGGAGTGGG[G/T]TGGAGGCCTGGTTGC	54472
rs112719982	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287804	CTCCCTGCCGCAGCC[C/T]CCCCGCCGCAGCCTC	54472
rs112732933	snp	C/G	0	0	splice-donor-variant, intron-variant	TOLLIP	GRCh38.p7	11:1288623	CAGGCGTGCAGCTCA[C/G]CGCGTAGGACATGAC	54472
rs112740638	snp	C/T	0.00993419	0.0697739	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276155	CAAGCTGTCAGCAGT[C/T]GGCTGGCAGTGCCAC	54472
rs112842927	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1277689	CGGAATGTCACGCCC[A/G]CTGATCCAAACACTG	54472
rs112901594	in-del	-/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1284356	GGGCTGGTGGTTTTC[-/T]TTTTTTTTTTGAGAT	54472
rs112929704	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1291380	CCCCGGGAGCCATCC[C/T]GGCCCTCCCACCCAC	54472
rs113133696	snp	C/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1294948	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACGGTG	54472
rs113314204	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1279842	GTAAGTCCCGGCCGC[C/T]GGTGGGCAGGGGAGC	54472
rs113471882	in-del	-/G	0.5	0	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304158	GGGACATCCACTCCC[-/G]GGGCTGCTCAGCAGC	54472
rs113544269	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310639	CCTCGTGCTTTTGGG[A/G]ACACCCTGCTCTATG	54472
rs113644457	snp	C/T	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1287904	CCCTGCTGCACCCTC[C/T]CTGCTGCACCCTCTC	54472
rs113726728	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294403	GCATGGCTCAGTGTG[C/T]CTCCTTTCCCTGCAT	54472
rs113732307	snp	A/G/T	0	0	splice-acceptor-variant, intron-variant	TOLLIP	GRCh38.p7	11:1286094	GCAGCTGGAAGCAGC[A/G/T]GAAACACAGCGGAGA	54472
rs113801730	snp	A/G	0.0170251	0.090679	intron-variant	TOLLIP	GRCh38.p7	11:1292848	CCAGCTAGGAGGACC[A/G]GGTATGCGGGCTGCA	54472
rs113859207	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297648	GAGAAGCCGTACTGC[A/G]AGAACAAGCAGAGCA	54472
rs113959389	snp	A/G	0	0	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302335	CTGACCCCTCAGTGC[A/G]CAGGGTTTCAGAGAC	54472
rs113978854	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294744	TGTCTCCTTTCCCTG[C/T]ATTTCTACGAAAGCC	54472
rs113979255	snp	A/G	0.229429	0.249152	intron-variant	TOLLIP	GRCh38.p7	11:1295054	GCCTGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs114044218	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1277684	CTACACGGAATGTCA[C/T]GCCCGCTGATCCAAA	54472
rs114503583	snp	A/G	0.00874735	0.0655527	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274543	GCCTGGCACCCTGCA[A/G]GGTAGCGCCCAGGGA	54472
rs114959412	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311384	CGTGCCACCCCCTGG[C/T]GGCGGGGCCCCCCAC	54472
rs115040064	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303707	AACCAGGGGCCTGTC[A/G]GGCAGGTCAAGGGAC	54472
rs115050982	snp	A/G	0.00318978	0.0398085	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299797	GAGCACAGGATGCCT[A/G]AGGCTGCGTCACCTG	54472
rs115437483	snp	A/C/T	0.0119091	0.0762411	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300573	TTCCTGTTGGTGACA[A/C/T]GTCTCCAACGGAGAG	54472
rs115849875	snp	C/T	0.169061	0.236535	intron-variant	TOLLIP	GRCh38.p7	11:1287876	CTCTGCTGCAGCCTC[C/T]CTGCTGCACCCTCCC	54472
rs116033108	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1282546	TGAGTCAATGGGTCC[A/G]GCACACCAACATGGC	54472
rs116283238	snp	C/T	0.111606	0.2082	intron-variant	TOLLIP	GRCh38.p7	11:1287881	CTGCAGCCTCCCTGC[C/T]GCACCCTCCCTGCTG	54472
rs116593151	snp	C/T	0.00438332	0.0466095	intron-variant	TOLLIP	GRCh38.p7	11:1285587	GAGGTTCAGACACAA[C/T]GGCGCAGCGCAGGGC	54472
rs116701390	snp	A/G	0.0126979	0.078662	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299825	CTGTGCCGTCAAAAC[A/G]CCCCGTCCACCAGCC	54472
rs116844349	snp	A/G	0.0165278	0.0893908	intron-variant	TOLLIP	GRCh38.p7	11:1278487	TGCAGGGGTGTAAAC[A/G]GAGCAGACAGGGCTT	54472
rs116938768	snp	C/T	0.0185938	0.0946107	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310012	CAGTGACAGGCCCGA[C/T]ATCCCCTGCAGGGCG	54472
rs116939577	snp	A/G	0.0198696	0.0976729	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288639	CGCGTAGGACATGAC[A/G]AGGTTGATCATGCCC	54472
rs116941008	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293970	CGGTGTAGCTGTGCT[C/T]ACCACACCATGAAGC	54472
rs117392832	snp	C/T	0.00716266	0.059414	intron-variant	TOLLIP	GRCh38.p7	11:1305953	TCGCGGGGGCCCGCA[C/T]GGTACCCCTCGCAGG	54472
rs117431642	snp	C/T	0.0205511	0.0992634	intron-variant	TOLLIP	GRCh38.p7	11:1307357	ACACCTCAGCACTTG[C/T]CAGCACAGGCCCTGC	54472
rs117500947	snp	C/T	0.0984431	0.198823	intron-variant	TOLLIP	GRCh38.p7	11:1291384	GGGAGCCATCCCGGC[C/T]CTCCCACCCACATGG	54472
rs117572864	snp	C/T	0.0479149	0.147179	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303706	TAACCAGGGGCCTGT[C/T]GGGCAGGTCAAGGGA	54472
rs117595658	snp	A/G	0.00874735	0.0655527	intron-variant	TOLLIP	GRCh38.p7	11:1292013	ATCAAAGCTGTGGCC[A/G]GTCCTTTTAGGTCAA	54472
rs117663261	snp	A/G	0.0228947	0.104514	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310983	ACATCTTTGGGTCTC[A/G]GTTACCAGTCTCTCC	54472
rs117792684	snp	A/G	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1283840	AAGTTGGAGGAGACG[A/G]GGAGGATCCTCCTCA	54472
rs117924096	snp	C/T	0.0228947	0.104514	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311086	CAAGTTGTAGCTTAA[C/T]ATCCAGCCAATCCAC	54472
rs118054222	snp	C/G	0.0240643	0.107019	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309921	GAGTGGCGACAGGGC[C/G]TAGCCACCTGGCGGG	54472
rs118085196	snp	A/C	0.0221141	0.102801	intron-variant	TOLLIP	GRCh38.p7	11:1287905	CCTGCTGCACCCTCT[A/C]TGCTGCACCCTCTCT	54472
rs137867760	snp	C/T	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1278926	TTGGCCATCACCTGT[C/T]CCTGCCCATACAGCT	54472
rs137869091	snp	C/T	0.000153988	0.00877327	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295736	TCCAGCTGGACCTGC[C/T]GCTGCTGCTGTGTGG	54472
rs137973784	snp	A/C/T	0.000855554	0.0206651	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276784	AGAAGGAGAGACGCA[A/C/T]GTCCCAGGGACAGGA	54472
rs138201374	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301785	TCAGAGCTGGGACCC[A/G]CAGCAGGAAGACCTG	54472
rs138382715	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287839	CCGCACCCTCCCCGC[C/T]GCAGCCTCCCTGCCG	54472
rs138633100	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276923	GGCACAGAAGTCCAC[A/G]GGAGGGGGCGACACG	54472
rs138639196	snp	A/G	0.000297637	0.0121955	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277219	CGGGGGCAGGGCCAC[A/G]GGCACCATGCCGGGG	54472
rs138674686	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280674	AGGCTGGGGAGGCGC[C/T]GGACGCCCCACTTTC	54472
rs138690831	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302146	CACACCCAGGTCAGA[A/G]CTCAGTCTGGCCCAG	54472
rs138709550	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279086	GATGGGGAAGGGACA[G/T]GAGGAGGGGAACTGC	54472
rs138869815	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280991	TGTTGCCAGCCTGGC[A/G]GAGAGTCTCTGTCCA	54472
rs138899584	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291027	GTAGACCATGAGATT[C/T]GACTTCAGGCCAGGT	54472
rs139059803	snp	C/T	0.0111196	0.0737302	intron-variant	TOLLIP	GRCh38.p7	11:1295851	GGGCACAAAGCAGCC[C/T]GACAGCAGCTGCCCC	54472
rs139087935	snp	A/G	8.26685e-05	0.00642864	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277078	CAGGGAGTTGATGGC[A/G]GCATCCTTGTTCCCT	54472
rs139117968	snp	A/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1292748	ACCGTGGGGACACAC[A/G]GGCACCGCTGCTTTC	54472
rs139128352	snp	C/T	0.000188849	0.0097154	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288624	AGGCGTGCAGCTCAC[C/T]GCGTAGGACATGACG	54472
rs139149465	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292836	TGCAGGGAGTGACCA[A/G]CTAGGAGGACCGGGT	54472
rs139390926	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310217	GCAGGAGCCCCGCTC[C/T]TCTCCTGCTCGCTCC	54472
rs139507547	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303757	AACAGAGGTTAGGGC[C/T]GGGTGCAGTGGCTCA	54472
rs139544999	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276002	CCTAAAATCTGTCCT[A/G]TAGGCCAAGATGCTA	54472
rs139605906	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309234	CTCCCCAAAGCTCTG[C/T]CCCGGCACGGCGGTG	54472
rs139741446	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279763	CAGGAAAACCAAAAC[C/T]TGTCCCTTTTCCATT	54472
rs139750280	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281815	CGACACACATGCTCT[A/G]GCCAAGATGCACTTT	54472
rs139784409	snp	C/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279543	CCGGGGCAGCCCAGA[C/G]CCCACCTGTAGCGGC	54472
rs139965382	snp	C/T	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298530	TTGCTCTGCACTCTT[C/T]AGGTGTCCGTTAAAG	54472
rs139967607	snp	C/G	0.00517822	0.0506191	intron-variant	TOLLIP	GRCh38.p7	11:1277596	GATCCCTTCAGAACT[C/G]GTGAATTTGCACTGC	54472
rs140032126	snp	C/T	0.00716266	0.059414	intron-variant	TOLLIP	GRCh38.p7	11:1286659	CAAAACTGTCAACTG[C/T]GGATAAGTCACTGCA	54472
rs140337138	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1306474	CCCTGGGGAGCATCT[C/G]TTTCTGCTGGAAAGC	54472
rs140374060	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278492	GGGTGTAAACGGAGC[A/G]GACAGGGCTTGCCAC	54472
rs140439497	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277422	TGGAAAGGCAAACCC[C/T]CAAACAGCAACCCCA	54472
rs140442022	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301291	CGATGGGCTAAATAC[A/G]TTCTGTGGAATTAAA	54472
rs140514207	snp	C/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1277908	AAAACTCAAACAAGT[C/G]GGGCAGCAGGTGCGG	54472
rs140626415	snp	C/G	0.0166325	0.0896639	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310946	CACCATGTGCTCTCA[C/G]TTTCCTCTTATCCCA	54472
rs140857999	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311387	GCCACCCCCTGGCGG[C/T]GGGGCCCCCCACCGT	54472
rs140876532	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287834	CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs140929037	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304681	GCAGAAGCTGATAAG[C/T]GCATGTTACCATTTC	54472
rs140976602	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306162	AGGGAAGCACTGCAC[A/G]GGGCTGAAGCATCCC	54472
rs141097873	snp	C/T	0.00104498	0.0228342	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290259	GATAGAAAGAGTCCA[C/T]GCCTGGGGGCACCGT	54472
rs141149652	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275581	GCCTTTAGGACCCAC[A/G]GCTGAAGAAGGCGCC	54472
rs141188303	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280725	CACCAAGCAGAAGGA[A/G]GTGGAAAGCAACAGG	54472
rs141565986	snp	A/G	0.00113638	0.0238097	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290311	GCGGGGATTCTTGGC[A/G]CCATTGTGTGCCGTG	54472
rs141603148	in-del	-/C			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290173	GGTGTGTCCCCACGG[-/C]CAGCCACGCTCAGCC	54472
rs141700822	snp	A/C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285169	CCCCCAACACCACCA[A/C/T]GCATCCCTAGCGCCC	54472
rs141798689	snp	A/G	0.00597247	0.0543191	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302703	CCACGCCAGTCTCCT[A/G]GCACTGGCATGTTCA	54472
rs141833183	snp	A/G	0.000105448	0.00726037	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295675	GTTCAGTCGGCCCAC[A/G]GTGCCCACTGCGCCT	54472
rs142066785	snp	C/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274119	GCCTGGAAATGAAAA[C/G]GCACCACAGAACCAC	54472
rs142260383	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276630	GTGAGGGATTGTGTG[C/T]GCCTTAAATCAACAG	54472
rs142300746	snp	C/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280628	AGCACAGAATGAGCT[C/G]ATGCACACCCTGGTG	54472
rs142306287	snp	C/T	0.00676609	0.0577691	intron-variant	TOLLIP	GRCh38.p7	11:1282376	CCTAATGTTAAATGA[C/T]GAGTCAATGGGTGCA	54472
rs142573629	snp	C/T	0.0766824	0.180169	intron-variant	TOLLIP	GRCh38.p7	11:1294192	TTCCCTGCATTTCTA[C/T]GAAAGCCGTGTGGCT	54472
rs142610147	snp	G/T	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300606	CCGCTGCTTCCTTGG[G/T]CCACACTTTCTGCCC	54472
rs142637486	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274638	CCCGCCTGAGGCTCC[A/G]AGATGGCACAGTCAG	54472
rs142658126	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1295572	GAAATGCAGTATAAA[C/T]GCCGAAATCCGAAAT	54472
rs142714391	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289844	CATGCATGCTCTGTC[A/C]CTGGAAATCCCACCT	54472
rs142729339	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308039	ACCTTGGAGCATCGT[G/T]AAAAAGGACTTTTTC	54472
rs142776865	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305285	GGTGAGTGCGTTCCC[C/T]GCTGGCTCAGGTGCA	54472
rs142911670	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300393	ACGAAAGAAAAGAGG[A/T]CTCCAACATTCACTT	54472
rs142920490	snp	G/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1277536	TTGATCTTTCAAATC[G/T]CACCCGAGTCTGTTT	54472
rs142927331	in-del	-/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293458	GGCATCCCACTGGGG[-/C]CCCAGGAGACAACAA	54472
rs142928640	snp	A/G	0.00072164	0.0189815	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288755	GGGTCCAGGCAATGC[A/G]GTCGTCCATGGAGAA	54472
rs143013859	snp	C/T	0.00180058	0.0299508	intron-variant	TOLLIP	GRCh38.p7	11:1286138	AAGGAGGAACATCCA[C/T]CCATCAGAACCTCGG	54472
rs143078447	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1281887	CATGCTTGCCTAGTC[A/G]GCCCGAGACGCCCTG	54472
rs143124042	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278406	GTTCCTTTCTACACT[C/T]GGAGGATCCTAAAGG	54472
rs143125868	snp	C/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1292780	CCACAATGGGCAAGA[C/G]ATGCGCGGCAGACAC	54472
rs143130045	snp	C/T	1.67351e-05	0.00289263	missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290388	CCATGCGGGTCATGC[C/T]GTAATTCTTGGCCAA	54472
rs143144151	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293785	GGTCACCAGGCCCTG[A/C]CAGGAGGTGGCGGCT	54472
rs143210443	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290497	CTCCCTGAACCCTTC[C/T]ACGAGGCCTTTTCCT	54472
rs143406220	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1278997	GCCTGTCCCTGCCCA[C/T]ACGTCTCCCCACAGC	54472
rs143476615	snp	A/G	0.00190964	0.0308411	intron-variant	TOLLIP	GRCh38.p7	11:1277287	TTTGGTAAAAACGTC[A/G]GAAAGTTCCAGAAGT	54472
rs143558857	in-del	-/A	0.0640965	0.167152	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309727	GCTCCAGGGTAGGGC[-/A]GGCGCAGCCTCTCGC	54472
rs143573396	snp	C/T	0.00398564	0.0444627	intron-variant	TOLLIP	GRCh38.p7	11:1280495	TGACGGGAGGGACTG[C/T]GCCGGTGAGGACGTG	54472
rs143854023	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1307382	CCCTGCGTGTGAGAA[C/T]ATCTCCTGCCGCTCC	54472
rs143888433	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288496	CCTCTGTCCTCAGAA[C/T]GTGAGCCCTGCTGTT	54472
rs144024538	snp	C/T	3.37171e-05	0.00410578	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288638	CCGCGTAGGACATGA[C/T]GAGGTTGATCATGCC	54472
rs144146461	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274951	TACAGTAAGCCACTT[C/G]TACAGTAAGCCTTCA	54472
rs144191022	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279555	AGAGCCCACCTGTAG[C/T]GGCCCTGGGAGGAGT	54472
rs144249750	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1278002	GCTACGCAGGCCCCT[C/T]GCCCCATGTCTGATG	54472
rs144319382	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279128	TGACGGTGGCTGTGA[C/T]GCTGCGACGTCACGG	54472
rs144425237	snp	A/G	0.000687107	0.0185225	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277182	CCTCCTCGCTACAGC[A/G]GGGCTGGGCGTTCAC	54472
rs144473473	snp	C/T	0.0178098	0.0926698	intron-variant	TOLLIP	GRCh38.p7	11:1287310	ATCGTCACTCACGGC[C/T]GGGACATGATTTAAA	54472
rs144679601	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287836	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCTG	54472
rs144692249	snp	A/G	0.00636936	0.0560724	intron-variant	TOLLIP	GRCh38.p7	11:1286763	AAAACTGTCCACTGC[A/G]GATAAGTCATTGCAC	54472
rs144799396	snp	C/T	0.00271739	0.0367602	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309562	GGCGACCTCCTGCGC[C/T]CCCGCCGGAGCCTGC	54472
rs144901649	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287829	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs144956879	snp	C/T	0.000184804	0.00961082	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290272	CACGCCTGGGGGCAC[C/T]GTGCAGTGGATGACC	54472
rs145057686	snp	C/T	0.00358779	0.0422022	intron-variant	TOLLIP	GRCh38.p7	11:1306311	GAAGCTCCCTCTACC[C/T]AAGGACAAAAGAACC	54472
rs145151092	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310351	GGCTGCATCCCCAGG[A/G]GTCGGGCGTTTACGG	54472
rs145251117	snp	A/G	0.000116857	0.00764295	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290344	CGTCTCGTACACCGC[A/G]TAGCCCAGGCGCAGT	54472
rs145409553	snp	C/T	0.000153988	0.00877328	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277047	AGAGGCTCTATGGCT[C/T]CTCCCCCATCTGCAG	54472
rs145433418	snp	C/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274359	TTAAAAAATACTCGG[C/G]AACAAACATGGTAAA	54472
rs145435385	snp	A/G			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311040	GCCTGTTTTGATGGG[A/G]TGTAGAGAAAAAGAA	54472
rs145435743	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1284051	GGCTCTGGGCTGTCC[C/T]AGTTACAAATCAGAA	54472
rs145462738	snp	C/T	0.00517822	0.0506191	intron-variant	TOLLIP	GRCh38.p7	11:1287056	CTCTGAGTTCAAAAC[C/T]GTCAGCTGCGGATAA	54472
rs145505029	snp	C/T	0.00636936	0.0560724	intron-variant	TOLLIP	GRCh38.p7	11:1307166	AAGTCACATGTACTC[C/T]AAGCAACACCTGAGA	54472
rs145542060	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280420	CGGGCATTCATGTCC[C/T]GGTCTGGTTGGCTCC	54472
rs145578982	snp	C/T	0.000417079	0.0144349	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295686	CCACGGTGCCCACTG[C/T]GCCTCCGTACTGCAG	54472
rs145616541	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276214	TGCCTCTATCACCTC[C/T]CACCCCAGCCTCGCA	54472
rs145694209	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1277707	GATCCAAACACTGCA[C/T]GGTCTGAGCCTCTTC	54472
rs145715290	snp	C/T	0.000142035	0.008426	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276762	GAGCATTTTCCAGAA[C/T]GGCATGAGAAGGAGA	54472
rs145749182	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280632	CAGAATGAGCTCATG[C/T]ACACCCTGGTGCTGC	54472
rs145801768	in-del	-/TGGGGCCATAAGGGTGCCGGGACCGCCTCCACCTG			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308813	ACAGCCATCATCTAT[lengthTooLong]GGGACCAACTAGAGT	54472
rs145957069	snp	C/T	0.00306418	0.0390244	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295774	GCGGAGGAAGTCCTG[C/T]GGGAGCTCACCGATG	54472
rs146009358	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298324	ATGCCCTCCTGGCCA[C/T]ACGTGGGGGACAGAC	54472
rs146052031	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1282061	CACTCTACAGTACTG[C/T]TAGGATAATTAAAAA	54472
rs146156644	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1286277	GGGCCCTGCTCCCAC[C/T]CCTGCACCACCTCCT	54472
rs146173649	snp	A/G	0.0103295	0.0711199	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298996	TGCTGGGACAGCAGG[A/G]GACAGTCATCGAAAA	54472
rs146176131	snp	C/T	0.000140252	0.00837297	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286056	TTGGCATCAGGACCA[C/T]GGGCTGGGGTGGCAT	54472
rs146203970	snp	A/C	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1283430	CATCTAGATGGCCGT[A/C]CTGTGCCAGGGACGC	54472
rs146305309	snp	C/T	0.00525193	0.0509743	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295747	CTGCCGCTGCTGCTG[C/T]GTGGGCGTGATGCGG	54472
rs146354036	snp	C/T	4.96085e-05	0.00498014	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277077	GCAGGGAGTTGATGG[C/T]GGCATCCTTGTTCCC	54472
rs146373282	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1281769	CACAGGCTTCTCCAC[C/T]ATGTGAGTCATAAAC	54472
rs146395933	snp	C/G	0.0103295	0.0711199	intron-variant	TOLLIP	GRCh38.p7	11:1279438	ATGTGTCAAGGCTGC[C/G]TGGGGACTTCAGGAG	54472
rs146558058	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279743	CTGACAAACACAAGG[A/G]TACCCAGGAAAACCA	54472
rs146576090	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278102	CACCCCTGAAGGCAC[C/T]GTGTGGCCGGACTTA	54472
rs146674626	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1293958	AGGAAGGGGTGACGG[C/T]GTAGCTGTGCTCACC	54472
rs146695170	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290886	TGCACATAATTCAGA[C/T]GCCACGTGGCTGCTT	54472
rs146905441	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301055	GTCGAACGAAGTTCA[A/G]TTAAAAACTAAAATG	54472
rs146941932	in-del	-/CCC			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290525	CTAACACATAGACTA[-/CCC]CAGCCACTCAGAGTC	54472
rs147049561	snp	C/T	0.000116966	0.00764652	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290323	GGCGCCATTGTGTGC[C/T]GTGGGCGTCTCGTAC	54472
rs147065932	snp	A/G	0.000750932	0.0193624	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277174	TTTCAGGTCCTCCTC[A/G]CTACAGCGGGGCTGG	54472
rs147151682	snp	C/G/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279040	GGAACGGAGGCACCG[C/G/T]GCTCCCACTCTCTCC	54472
rs147169583	snp	C/T	0.00874735	0.0655527	intron-variant	TOLLIP	GRCh38.p7	11:1277341	AAGAAAACAACGCAT[C/T]CCACCGGCCTCCCTG	54472
rs147184845	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1287065	CAAAACTGTCAGCTG[C/T]GGATAAGTCACTGCA	54472
rs147274796	snp	A/C/G	0.00106201	0.0230194	intron-variant	TOLLIP	GRCh38.p7	11:1288613	CCACCCCGCCCAGGC[A/C/G]TGCAGCTCACCGCGT	54472
rs147375873	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308519	CAGCAATGCAAGAAG[A/G]CCCTAACAGTGAGCC	54472
rs147639903	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280562	GTGTGAAATGGAGGT[A/G]CACGAGGGAACAGAT	54472
rs147728317	snp	C/T	0.0115144	0.0749975	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300582	GTGACACGTCTCCAA[C/T]GGAGAGAGCCGCTGC	54472
rs147866259	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301199	AATATCCTTAGTGAA[C/T]TGAAGCTTTTGCTTG	54472
rs147873040	snp	C/T	0.000501655	0.0158296	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290303	TTATTCCAGCGGGGA[C/T]TCTTGGCGCCATTGT	54472
rs147955595	snp	A/G	0.00358779	0.0422022	intron-variant	TOLLIP	GRCh38.p7	11:1304898	TCTCTTAACTAGAAA[A/G]ATGAAACTAGCGCAT	54472
rs148001930	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1284972	TTTCTGCATCTGTGC[A/G]GGATGCTGGCAGGAC	54472
rs148038404	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311117	AGCACAAGACCCAAG[A/G]AGCTATTAACCACAA	54472
rs148070720	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302917	CCTTCCGGGGCCTTC[C/T]TCAGACAGGGCTTTC	54472
rs148251270	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278407	TTCCTTTCTACACTT[A/G]GAGGATCCTAAAGGC	54472
rs148253939	snp	C/T	0.0010734	0.0231419	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295659	CCTGTACCACCGTGA[C/T]GTTCAGTCGGCCCAC	54472
rs148370374	snp	C/T	0.202651	0.245475	intron-variant	TOLLIP	GRCh38.p7	11:1287850	CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCTCTG	54472
rs148472983	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289669	GGTGAGCGGCCAGAC[A/G]AGTGCCCAGTGGACA	54472
rs148529381	snp	A/C/G	0.00914312	0.0669923	intron-variant	TOLLIP	GRCh38.p7	11:1286985	AAGTCACTGCACCGC[A/C/G]GTTGTCTCTGAGTTC	54472
rs148650184	snp	A/G	0.00914312	0.0669923	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299984	AAGGAGGCCTCTGTC[A/G]ACACCAACTCTGGAG	54472
rs148701571	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275157	CTGTGTGGGTCCCTC[A/G]GGCCCCCACACGGGC	54472
rs148718519	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1282104	CTCCTAAAAGCAGTG[C/T]TCTCCTAATGGGAAC	54472
rs148775939	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279153	TCACGGCCTGGGGTG[C/T]CCCGAGAAACCTGCT	54472
rs148849410	in-del	-/G			intron-variant	TOLLIP	GRCh38.p7	11:1285772	TTCTGCCAACAATTA[-/G]AAAAAAAAAAAAAAA	54472
rs148880016	snp	G/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280429	ATGTCCTGGTCTGGT[G/T]GGCTCCACAGAAACC	54472
rs149013801	snp	A/C	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1304926	CATTCCCATCAAAAG[A/C]CTTAGTCTTCTTAGA	54472
rs149141495	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310607	ATAAACAAGCGTACC[A/C]AGGTGGACGCCTTCC	54472
rs149174945	snp	C/T	5.00856e-05	0.00500403	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290360	TAGCCCAGGCGCAGT[C/T]GGCAGTAGGGGTCCA	54472
rs149230501	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276536	ACCCAAGCCCTGGGC[A/T]GGGGCCAGGCTCACA	54472
rs149279819	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1279113	CTGCTGCAAAATCGA[C/T]GACGGTGGCTGTGAC	54472
rs149336361	snp	C/T	0.000198946	0.00997162	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286023	TGGGCACATAGCCAA[C/T]GCCCTGCTGGTACAC	54472
rs149350458	snp	A/G	0.0197687	0.0974348	intron-variant	TOLLIP	GRCh38.p7	11:1286727	TGTGGATAAGTCACT[A/G]CACTGCTGTCTCCTG	54472
rs149364877	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1296462	CCCGCACACCTGCAG[C/T]GGCCGAAGGGGCCTG	54472
rs149401232	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1281339	TGACCTCAGCGCCCC[A/G]GCTTCTGAGTTGCTT	54472
rs149526211	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293058	GGCAGTGGGTGGGTG[C/T]GGGGGGCTCCAGGCC	54472
rs149545648	snp	C/T	0.00875628	0.0656872	intron-variant	TOLLIP	GRCh38.p7	11:1307310	ATGATGGAAACAGCC[C/T]AGGAGGCACTGGGCA	54472
rs149598328	snp	C/G	0.00517822	0.0506191	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301890	CTAGGGATATGGGCG[C/G]AAGTCAGTCTCAAAG	54472
rs149804862	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280116	GTGATAGTTTGTCTC[A/G]GAAACTTTTAAGCAT	54472
rs149855698	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1277665	CTCTGCATCTGGGGA[C/T]GGACTACACGGAATG	54472
rs149893655	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299779	ATGCTCACTCGGGCA[C/T]GTGAGCACAGGATGC	54472
rs150068184	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310309	CCAGCTCGAACAGCG[A/C]TGGGTAAACTGAGGC	54472
rs150240433	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291010	AAGGAGCCACATCAC[A/G]TGTAGACCATGAGAT	54472
rs150377920	snp	C/G/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278751	GCCTTTCGGCAATGA[C/G/T]GGAAAACGAACCGAA	54472
rs150415585	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301448	AGATCGCACATGTGT[C/T]GCGGGCTTCCGAGAA	54472
rs150466681	snp	C/T	0.00358779	0.0422022	intron-variant	TOLLIP	GRCh38.p7	11:1295168	CGGCGTTCAATCTGC[C/T]GATTTTGGCTTTCAC	54472
rs150516908	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303446	CCATGGTGAGGTGCT[A/G]GGGCACCCCTGCTCC	54472
rs150577484	snp	C/T	0.00179301	0.029888	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277204	GGCGTTCACGGCGGC[C/T]GGGGGCAGGGCCACG	54472
rs150584968	in-del	-/CCACCCTGT			intron-variant	TOLLIP	GRCh38.p7	11:1291582	CCTCTGAGGGCACGG[-/CCACCCTGT]CCTCACTGAACCCTC	54472
rs150673853	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1277542	TTTCAAATCTCACCC[A/G]AGTCTGTTTTATAAC	54472
rs150726502	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275775	GACTAAAATGTAAGC[A/G]CTAACTTCCTCCTTC	54472
rs150764394	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1292787	GGGCAAGAGATGCGC[A/G]GCAGACACACAGCGC	54472
rs151017610	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1283801	GCACCCCCCAAAAAG[A/C]CAGCCACAGAGCGCC	54472
rs151039898	snp	C/G	0.0193772	0.0965046	intron-variant	TOLLIP	GRCh38.p7	11:1305354	AGAGCCAGCGGAGAC[C/G]GGTAAGTGCCACTGG	54472
rs151101451	snp	A/G	0.000201643	0.010039	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288759	CCAGGCAATGCGGTC[A/G]TCCATGGAGAAGGCT	54472
rs151185390	in-del	-/CA			intron-variant	TOLLIP	GRCh38.p7	11:1277856	CCAGAATGACAACCC[-/CA]CACACACATACAAAC	54472
rs151256822	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276670	AATTACATCACATCA[A/C]AAAATGCCATGAATG	54472
rs151272471	snp	C/T	0.0209421	0.100162	intron-variant	TOLLIP	GRCh38.p7	11:1282517	GTTTAGGAGAAATAC[C/T]TAATGTTAAATGATG	54472
rs180703833	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1278901	CCCCGGCTGGCAGGC[A/G]GGCAGGAACTTGGCC	54472
rs180764195	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304536	GGCACAGCAGCACCC[A/G]CGCCAGGACGGGGCG	54472
rs180879083	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1307928	GAAGAATTATCTCCT[C/T]GGGAGAAACACCAGG	54472
rs181257871	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276017	GTAGGCCAAGATGCT[A/G]CACGCAGCGCCCAGG	54472
rs181280088	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279372	TGAGCCGGCCCATCC[C/T]GGTTACCAAGCACGG	54472
rs181336373	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1287990	AAATCCTCTGGTTGA[C/T]GATACAGACGAGACG	54472
rs181411651	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1305161	AGTGAAAAGATGTGA[C/T]TTCCAGGCAAGCACA	54472
rs181414598	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287549	AGCCTCACCGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs181416898	snp	C/G/T	0.0103426	0.0713021	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276119	CCCACGCTGAACCCA[C/G/T]GTCCTGGGCACAGCA	54472
rs181419904	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1284434	GCTCACTGCAAGCTC[C/T]ACCTCCTGGGTTCAC	54472
rs181565656	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280113	CATGTGATAGTTTGT[C/T]TCGGAAACTTTTAAG	54472
rs181568209	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293458	GGCATCCCACTGGGG[C/T]CCCAGGAGACAACAA	54472
rs181571320	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1288529	ATGGGCTCAGTGCCT[C/T]CAGGAAAGAGACAAG	54472
rs181706951	snp	G/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308451	CAGCCTGCAGAACCG[G/T]GAGCCAATTAAATCT	54472
rs182004927	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287794	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs182032389	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1306552	TAACAGAAAGAGGAC[A/G]TGATAAATACTGTGT	54472
rs182088877	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304087	GGAGGCAGGCCAGAA[A/G]CAGCGTATTCAGAAG	54472
rs182108346	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274546	TGGCACCCTGCAGGG[C/T]AGCGCCCAGGGAGCA	54472
rs182118263	snp	A/C	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1305590	ACAATCCCAGTTAAT[A/C]AACACCGAAGAAGTG	54472
rs182130262	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287738	CTGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs182272730	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285105	GCAGCCCCTGAGCAC[A/G]AGCAGCCGGGGCCTC	54472
rs182300044	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1285620	GCGTCACCCAATGGG[C/T]GTGAGGTTCGGACAC	54472
rs182308113	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298884	CCCTGACCAGTCAGT[C/T]GTCCTCAAACCGTCA	54472
rs182394425	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1287306	ACACATCGTCACTCA[C/T]GGCCGGGACATGATT	54472
rs182446518	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1293950	ACGCCGCGAGGAAGG[G/T]GTGACGGTGTAGCTG	54472
rs182516011	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297975	GATTCACAGCCCAGA[A/G]CTCTCTCCCCGGGGG	54472
rs182606533	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310417	ACCCGGAACTTAGGT[C/T]CCGATGTCCGGGTAT	54472
rs182611353	snp	C/T	0.000142643	0.00844401	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276717	CACCACCTCCAACAC[C/T]CTGGCAGAAGCAGCT	54472
rs182713922	snp	C/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280927	CCAGTGGCACCCGCG[C/G]TGGTCTCTCACGCAC	54472
rs182822698	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1281907	GAGACGCCCTGAGCA[C/T]GCAGCCGCCAGCCTC	54472
rs182958165	snp	C/T	0.00358779	0.0422022	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299869	CAGCGCATCGCCACG[C/T]GGCCTCACCAGGAGC	54472
rs183058617	snp	C/T	0.00517822	0.0506191	intron-variant	TOLLIP	GRCh38.p7	11:1282761	GTTGTGCACATGTAC[C/T]CTAAAACTTAAAGTA	54472
rs183090346	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1295551	AAGTTCTGTTTGCCC[A/G]CTTAGGAAATGCAGT	54472
rs183400443	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276432	GCCTTCAGGCCGGAG[C/T]CTGTCACAAGGCTGG	54472
rs183430958	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289318	GGCAGGGAGGGCTGG[C/T]CGTCTGCTGGCCTGG	54472
rs183432839	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274176	GAAGAGCAGACCCAC[A/G]CCCACTGCCACTGTT	54472
rs183485200	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305316	GTCAGCAGGAACGGA[C/T]GCCCTCCCAGGAGCA	54472
rs183602541	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311075	AGCCCCTTCCTCAAG[C/T]TGTAGCTTAACATCC	54472
rs183669349	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1286683	CACTGCACCGCTGTC[A/G]TCTCTAAGTTTAGTT	54472
rs183679660	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301837	GACAGAGGAAGCTAA[A/T]GAAACAGAGAGAAAT	54472
rs183721096	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287801	ACCCTCCCTGCCGCA[C/G]CCTCCCCGCCGCAGC	54472
rs183732213	snp	A/C	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275802	CTTCTGCATCTTCCA[A/C]AGAAGACCCACTTGT	54472
rs183751330	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1306828	CATCCTCGGCCCCTG[A/G]GGCTCCCTCCTCTCC	54472
rs183814747	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1283893	CTGCCTACGGGGCTT[C/T]GACTTCCAGCCTCAG	54472
rs183821506	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1297422	TGAGTAAACAGAAGG[A/G]ACCCGGACGATCCAG	54472
rs184060576	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1286487	CTGCTGTCAACTCTG[A/G]GTTCAAAACTGTCCA	54472
rs184245356	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301021	AGTCTCAGCGCTAAC[A/G]CCAGGTTAGCATAAC	54472
rs184264076	snp	A/T			intron-variant	TOLLIP	GRCh38.p7	11:1296813	AGGCCTGGTTGATGG[A/T]GGAGTGGGGTGGAGG	54472
rs184375012	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283629	TCAAAGTTTGTCTAG[A/C]CTTTCCTAAAATAAA	54472
rs184409585	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1279349	GGGCAGAGGCCATGT[A/G]CCTGGCCTGAGCCGG	54472
rs184441602	snp	A/G	0.0107246	0.0724382	intron-variant	TOLLIP	GRCh38.p7	11:1291580	CCCCTCTGAGGGCAC[A/G]GCCACCCTGTCCTCA	54472
rs184460247	snp	C/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1277544	TCAAATCTCACCCGA[C/G]TCTGTTTTATAACTA	54472
rs184568508	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292687	GGACACACGGGCACC[A/G]CTGCCTCCCCCACAA	54472
rs184604196	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275404	GGAACATACCATCTA[A/G]AACGTTCCAGTCCCG	54472
rs184973113	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287764	CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs185068029	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305969	GGTACCCCTCGCAGG[G/T]GCCCCCATGATACTC	54472
rs185077564	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275156	ACTGTGTGGGTCCCT[C/T]GGGCCCCCACACGGG	54472
rs185092938	snp	A/C	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1277841	AGCTGCAGCCGATGC[A/C]CAGAATGACAACCCC	54472
rs185100415	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303773	GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAAA	54472
rs185101481	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1291847	GGGCACGGCCGCCCC[A/G]TCCTCACCGACCCCC	54472
rs185231686	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306222	GAAGATCTAAACACG[A/G]TATGATTCTCTCAGA	54472
rs185233508	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1287163	CGAAACTGTCAACTG[C/T]GGATAAGTCACTGCA	54472
rs185334616	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287780	CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCTG	54472
rs185370957	snp	C/T	0.147991	0.228242	intron-variant	TOLLIP	GRCh38.p7	11:1287391	AAAGCAGCTCCCTGC[C/T]GCTGCCTCCCCGCCG	54472
rs185389355	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1287470	CCCCGCCGCAGCCTC[A/C]CCGCCGCACCCTCCC	54472
rs185423253	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1304753	TTGAGATAAAACAAC[C/T]GAATTTTTTAAAACT	54472
rs185500124	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304279	CGCCCACCTGGAGTT[C/T]CACACACACAAAAAT	54472
rs185537236	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1285635	CGTGAGGTTCGGACA[C/T]GACGGCACAGTGCAG	54472
rs185541383	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298933	GAAAGCCTGAGAGAC[A/G]GTCCCAGATTGGAGA	54472
rs185803648	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1279773	AAAACTTGTCCCTTT[C/T]CCATTCAGGAAAAAT	54472
rs185839057	snp	A/G	0.00478085	0.0486577	intron-variant	TOLLIP	GRCh38.p7	11:1293233	CCGGGAGGGTGGCCC[A/G]AGAGCTCCACCTTGG	54472
rs185912389	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298459	GCACTGTGGGTCCCT[C/T]GCTGCTCTGGATCCT	54472
rs185939754	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297750	GAGGAGGGTGCAGAG[C/G]TGCCTGAGCGGAGTG	54472
rs185979803	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1288832	GGGGCCACCCTGCCC[C/T]TGCAGCCGCACCATC	54472
rs186053820	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1285362	GGCTGCGGTCTCCCC[A/G]CCTGCTAAAGACGGC	54472
rs186077489	snp	A/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280973	AATTGAGCAGTTGGC[A/T]GCTGTTGCCAGCCTG	54472
rs186107355	snp	A/C	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293769	AGGTGGAGTGCCCTG[A/C]GGTCACCAGGCCCTG	54472
rs186191440	snp	G/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1294004	TGAAAGCAAGTCTTA[G/T]TTGTGAGGTCCACGG	54472
rs186194176	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288107	AGCCAGGGCGCTGAC[A/G]TGCTGGCCCCACAGC	54472
rs186292000	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276023	CAAGATGCTACACGC[A/G]GCGCCCAGGCAGTCA	54472
rs186348700	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308013	CAGTACTGGGCTGCG[C/T]GAGGGCAGGGACCTT	54472
rs186644202	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276561	CTCACAGCAAAGCGC[A/G]TTAGGGCAAGGGCGT	54472
rs186650388	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289424	ACTGAGCAGCAGCCT[C/T]GCCACATCCCCTCTG	54472
rs186749964	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275094	GAGATGGCGGCAAGC[A/G]TGGTCATCGGCAAAG	54472
rs186752636	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305206	GTACAGACTCACAAC[C/T]CGGCCTAAAAAATCC	54472
rs186781358	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287745	AGCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs186856671	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1284584	TTGATCTCCTGACCT[C/T]ACGATCTGCCCGCCT	54472
rs186894039	snp	C/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302055	TGCTGTGTCTGAGGG[C/G]CTGGCCCTGCCTTGA	54472
rs186925025	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287680	CCCCGCCGCACCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs187220728	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1280190	ATGTGCTGCTCAGCT[A/G]CAAACTCCCTATTCG	54472
rs187500542	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1282262	ATCCCGCCTGAGGGG[A/G]CTCCCTCTGGCCAAA	54472
rs187505701	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1295397	TGGTGGAAGAGCCAG[A/G]CCCTACACAGAGCAG	54472
rs187565737	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274414	TCTATTTTTATATGG[A/G]TCATTTATTAAATTA	54472
rs187604555	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287710	CCGCCGCAGCCTCCC[C/T]GCTGCACCCTCTCTG	54472
rs187626472	snp	C/T	0.00953873	0.0683987	intron-variant	TOLLIP	GRCh38.p7	11:1291634	CCGCCCTGTTCTCAC[C/T]GCACCCCTCTGAGGG	54472
rs187637433	snp	C/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1277564	TTTTATAACTAGCAG[C/G]CTGGGGGTGGTGTTT	54472
rs187659344	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1311385	GTGCCACCCCCTGGC[A/G]GCGGGGCCCCCCACC	54472
rs187771180	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286627	GGATAAGTCACTGCA[C/G]TGCTGTCTCCTGAGT	54472
rs187834909	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290588	GGCCAGGAGCAAGAA[A/G]AGTGAGCCACAGATG	54472
rs187993992	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275270	TGCACCCCAGCAACG[C/T]GAAGGCAGAAACCGG	54472
rs188125954	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310442	GGGTATCTTAAGAAC[A/T]AGAAGCATTCTTAGT	54472
rs188284387	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287766	CCGCCGCACCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs188438557	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286982	GATAAGTCACTGCAC[C/T]GCGGTTGTCTCTGAG	54472
rs188442912	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287808	CTGCCGCAGCCTCCC[C/T]GCCGCAGCCTCCCCG	54472
rs188472459	snp	A/C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1306914	CTCCCATTCCTCCTC[A/C/T]GAGAGATGTCACGTC	54472
rs188487646	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286422	GGGAACCACACTGCA[C/T]TGCTGTGGTGTCTGA	54472
rs188587492	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1284254	CTCTGAACGCCTCAA[A/G]GCTGCTTCTGCGTTT	54472
rs188591370	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1297612	GACTGGGACACGTCA[C/T]GAGTGACCTTTGCCC	54472
rs188665751	snp	A/C/T	0.00199529	0.0315338	intron-variant	TOLLIP	GRCh38.p7	11:1296388	CTCTGTCCACCACTG[A/C/T]CACTTCTGAGGGGAA	54472
rs188794338	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301057	CGAACGAAGTTCAAT[G/T]AAAAACTAAAATGCT	54472
rs188801479	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300348	CTCACTGACGCCAGA[A/G]CTCTAAACCACTGCA	54472
rs188908264	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1283098	CAGCCAGGCAGAGCC[C/T]GCCGTGAGGGACGAG	54472
rs189127265	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1293395	GGATGCAGAAGTCAC[C/T]GGGATGTGTGGGCAG	54472
rs189304692	snp	C/T	0.00676609	0.0577691	intron-variant	TOLLIP	GRCh38.p7	11:1283817	CAGCCACAGAGCGCC[C/T]GGCCCAGAAGTTGGA	54472
rs189347303	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287792	CCCCGCCGCACCCTC[C/T]CTGCCGCAGCCTCCC	54472
rs189368477	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275462	GAAATCTACACAGGC[A/G]TAAGACCAGGCCATC	54472
rs189487745	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292797	TGCGCGGCAGACACA[C/T]AGCGCAGCAGACGGC	54472
rs189500855	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304373	TCTAGATGAACCTGA[A/G]GCTAAAGGAAAGTGA	54472
rs189527480	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310308	TCCAGCTCGAACAGC[A/G]CTGGGTAAACTGAGG	54472
rs189608452	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275992	CCAGGTGTCACCTAA[A/C]ATCTGTCCTGTAGGC	54472
rs189626375	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297075	GTCTGCAGGGGCCCC[A/G]GTCAGCGCCAGTGCC	54472
rs189733280	snp	C/T	0.00716266	0.059414	intron-variant	TOLLIP	GRCh38.p7	11:1279362	GTGCCTGGCCTGAGC[C/T]GGCCCATCCTGGTTA	54472
rs190156264	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287472	CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCCG	54472
rs190156697	snp	C/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1287246	CGTCATGATGGTTCT[C/G]TGTTTGTATGAAAGC	54472
rs190188684	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1305115	AAGGCAAGAGGCCTT[C/T]ATCTTCCAAGAGGCC	54472
rs190190620	snp	C/T	0.00636936	0.0560724	intron-variant	TOLLIP	GRCh38.p7	11:1281468	GGTGGCAGCTGGGCT[C/T]AGACACCACGGGAGG	54472
rs190291294	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297814	CAGGCAGCCTCTCTC[A/G]AGGCGCTGTACAGCT	54472
rs190296422	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285749	CTGAAAATTTCAACT[C/T]ACCTCATTTCTGCCA	54472
rs190334482	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299459	TATCGTTTCAGTGAC[A/G]ACACTCGGTCCTTCA	54472
rs190386031	snp	C/T	0.00636936	0.0560724	intron-variant	TOLLIP	GRCh38.p7	11:1278870	GACCCCTGGGATCCC[C/T]GTGGCTTTTTGGGCG	54472
rs190393396	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303879	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG	54472
rs190559648	snp	A/G	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1284829	CAGGCAGTTTTGTCC[A/G]AGAATGTCCTGAACA	54472
rs190607240	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289889	AGATCAGTGCCCAGC[A/G]GAGGGGACACGTGCA	54472
rs190647016	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1292090	GCCACAGCGTACTCC[A/G]GAATGCTATGGAGTG	54472
rs190839632	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289052	GCGAGGGCCCTGGGC[C/T]GCTGTCCTCCTTCAG	54472
rs190853042	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276585	AGGGCGTGAGTTTTC[A/G]TCTGGGAAGTTCTAA	54472
rs190956035	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274459	AAAAATATATTTTAC[A/T]ATCAAAGAAAAATCT	54472
rs190967838	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1305480	CTTGAGGTACGGGAA[A/G]ATGAGGGAAAAGCAT	54472
rs190984476	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287713	CCGCAGCCTCCCCGC[C/T]GCACCCTCTCTGCCG	54472
rs191108119	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1294120	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs191128433	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1286676	GATAAGTCACTGCAC[C/T]GCTGTCATCTCTAAG	54472
rs191135690	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301319	AAATCACAAAATGTC[A/G]ACGATTCTCATTCAA	54472
rs191256399	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308363	ACGTGTAAGCTCCCA[C/T]TTGGCCTTCCGCCAT	54472
rs191484187	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1288448	GTGGGCAGGGCAGCC[C/T]CTCTCTGCCACCAAA	54472
rs191639026	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1283838	AGAAGTTGGAGGAGA[C/T]GGGGAGGATCCTCCT	54472
rs191648050	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305269	GGACTCGTGAGGAGG[C/T]GGTGAGTGCGTTCCC	54472
rs191673686	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297117	TTTTCAGGAAATACC[A/G]AGTGGAACCTGGAAC	54472
rs191769402	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287694	CCCCGCCGCAGCCTC[C/T]CCGCCGCAGCCTCCC	54472
rs191787005	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303174	TATAAAAGCTGACTA[C/T]AGAACAAGCGACTTT	54472
rs191810125	snp	C/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1286984	TAAGTCACTGCACCG[C/T]GGTTGTCTCTGAGTT	54472
rs191959620	snp	G/T	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1282294	CTGGAATAATTTGAG[G/T]GAAAAAATAACATTC	54472
rs191964470	snp	C/T	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1295550	GAAGTTCTGTTTGCC[C/T]GCTTAGGAAATGCAG	54472
rs192017024	snp	A/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1280531	AGCAGAGAAAAGAGA[A/G]AAGCACTCCAGGCCC	54472
rs192063872	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOLLIP	GRCh38.p7	11:1274074	TCTCAGAACGGGGTC[A/G]TGTTCCACGCTCACT	54472
rs192193034	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1292289	AGTCTGAGACCAGCA[C/T]GATTTTCCAAAGCTT	54472
rs192349109	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1293936	CAAGGGTCTGAGACA[C/T]GCCGCGAGGAAGGGG	54472
rs192485607	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291670	CCGCCCCGTCCTCGC[C/T]GACCCCCCGCTGAGG	54472
rs192497372	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1277702	CCGCTGATCCAAACA[C/T]TGCACGGTCTGAGCC	54472
rs192682468	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275128	TGCTCTCCCTCCAGC[A/G]AGGCTGGCCCCCACT	54472
rs192753547	snp	G/T	0.0017025	0.0291264	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277021	GAGCGGGGGCAAAAC[G/T]GCATCGAGGCAGAGG	54472
rs192761656	snp	C/T	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310982	CACATCTTTGGGTCT[C/T]GGTTACCAGTCTCTC	54472
rs192817057	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287773	ACCCTCCCCGCCGCA[C/G]CCTCCCCGCCGCACC	54472
rs192898159	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287752	CCGCCGCAGCCTCCC[C/T]GCCGCACCCTCCCCG	54472
rs192952885	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290899	GACGCCACGTGGCTG[C/T]TTTCCTCCCTCGTGA	54472
rs193029043	snp	C/T	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1306220	CTGAAGATCTAAACA[C/T]GGTATGATTCTCTCA	54472
rs193030847	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275283	CGCGAAGGCAGAAAC[C/T]GGTGCTGGTGGCCAC	54472
rs193085344	snp	A/C	0.00874735	0.0655527	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300710	GCCCCGGAAGAGCCC[A/C]GCTCAGCCCAGGACG	54472
rs193120829	snp	C/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1283216	CCTGCCAGCAGCCCC[C/G]GGGAAACTCAGCCCT	54472
rs193236650	snp	G/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1286468	CTTCACATAAGTCAC[G/T]GCACTGCTGTCAACT	54472
rs193282571	snp	C/G/T	0.00159649	0.0282165	intron-variant	TOLLIP	GRCh38.p7	11:1296449	CATCCCGAAACCACC[C/G/T]GCACACCTGCAGCGG	54472
rs199524160	snp	A/G	0.00699995	0.058745	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276994	GGGGAGCGCCGGGTC[A/G]GCGTGTCCAAAGAGC	54472
rs199578390	snp	C/T	6.70758e-05	0.0057908	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277181	TCCTCCTCGCTACAG[C/T]GGGGCTGGGCGTTCA	54472
rs199603176	snp	C/T	0.000521232	0.0161352	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276996	GGAGCGCCGGGTCGG[C/T]GTGTCCAAAGAGCGG	54472
rs199606088	snp	C/T	0.000522647	0.016157	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288764	CAATGCGGTCGTCCA[C/T]GGAGAAGGCTCTCTG	54472
rs199788465	in-del	-/AC	0.0437281	0.141251	intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304305	AAAATAGCTGTCAGG[-/AC]ACAGAGAAAAGGCAT	54472
rs199855632	snp	C/T	0.00100197	0.0223602	intron-variant	TOLLIP	GRCh38.p7	11:1295599	AAATCCCACCCCCAC[C/T]GAGCGCACCAGCCCC	54472
rs199861074	snp	C/G	0.000153988	0.00877328	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295663	TACCACCGTGATGTT[C/G]AGTCGGCCCACGGTG	54472
rs199896670	snp	C/G	8.35582e-05	0.00646314	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288747	GGTGATGTGGGTCCA[C/G]GCAATGCGGTCGTCC	54472
rs199981907	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1286578	GTCACTGCACCGCTG[C/T]CGTCTCTGAGTTTAG	54472
rs200039884	snp	C/T	6.98934e-05	0.00591116	intron-variant	TOLLIP	GRCh38.p7	11:1286132	GGGGTCAAGGAGGAA[C/T]ATCCACCCATCAGAA	54472
rs200215863	in-del	-/ACAT			intron-variant	TOLLIP	GRCh38.p7	11:1282909	ACCTGCACGTTGTGC[-/ACAT]GTACCCTAAAACTTA	54472
rs200240822	snp	C/T	0.00114172	0.0238654	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288758	TCCAGGCAATGCGGT[C/T]GTCCATGGAGAAGGC	54472
rs200356789	in-del	-/ACCCA			intron-variant	TOLLIP	GRCh38.p7	11:1297052	TGGAGTGGGGTGGAG[-/ACCCA]GCCGTCTGCAGGGGC	54472
rs200578328	snp	A/C/G/T	0.00108878	0.02331	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277010	GCGTGTCCAAAGAGC[A/C/G/T]GGGGCAAAACGGCAT	54472
rs200790260	in-del	-/ATAA	0.0558544	0.157504	intron-variant	TOLLIP	GRCh38.p7	11:1282630	TAAAATATAATTAAG[-/ATAA]ATAAATAAATAAAAT	54472
rs200810723	snp	A/G	0.000165303	0.00908978	intron-variant	TOLLIP	GRCh38.p7	11:1288818	CAGGCATCAGGGAAG[A/G]GGCCACCCTGCCCCT	54472
rs200881444	snp	A/G	0.00548886	0.052099	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1286024	GGGCACATAGCCAAC[A/G]CCCTGCTGGTACACT	54472
rs200928462	in-del	-/A	0.021333	0.101051	intron-variant	TOLLIP	GRCh38.p7	11:1287973	TTCAGTAACAGCCTG[-/A]AAAATCCTCTGGTTG	54472
rs200993320	snp	C/T	1.67503e-05	0.00289393	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288752	TGTGGGTCCAGGCAA[C/T]GCGGTCGTCCATGGA	54472
rs201099751	snp	C/T	0.000138663	0.00832539	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290447	AAAAGGAGGTGCCAA[C/T]CATCAGGAGAGGGTG	54472
rs201137588	snp	A/G	0.00199806	0.0315442	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288720	CTTGCCCTGCCTCAG[A/G]GACTCCGGGATGGTG	54472
rs201166699	snp	C/T	0.000433377	0.014714	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288699	GCTGTACCACTTGTC[C/T]TCCACCTTGCCCTGC	54472
rs201193280	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1281408	GTCCTCGTGAGGGCT[C/T]AGCCAGCATTCAGCC	54472
rs201304072	snp	A/G	1.66946e-05	0.00288912	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290339	GTGGGCGTCTCGTAC[A/G]CCGCGTAGCCCAGGC	54472
rs201394513	in-del	-/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308942	TCAGGGTGCGGGACC[-/C]GCCTCCACCTGGGGG	54472
rs201435614	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309659	CCCGGCACCGCCCCA[A/C]TGCGCAGGCGCCGCG	54472
rs201436284	snp	G/T	3.31219e-05	0.00406938	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277155	GGAACATGTCCTGGA[G/T]GGCTTTCAGGTCCTC	54472
rs201791881	in-del	-/TG			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274525	GTTCTGAGACCACTC[-/TG]CTGCCTGGCACCCTG	54472
rs201951123	snp	A/G	0.000188319	0.00970176	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288625	GGCGTGCAGCTCACC[A/G]CGTAGGACATGACGA	54472
rs202103427	snp	A/G	7.41826e-05	0.00608981	intron-variant	TOLLIP	GRCh38.p7	11:1295600	AATCCCACCCCCACC[A/G]AGCGCACCAGCCCCA	54472
rs202211815	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1294552	GGTGTGTCTCCTTTC[-/C]CTGCATTTCTACGAA	54472
rs202220655	snp	A/C	0.004072	0.0449379	intron-variant, utr-variant-5-prime, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295730	TGGGCGTCCAGCTGG[A/C]CCTGCCGCTGCTGCT	54472
rs202232442	snp	A/C			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290151	CCAGGAACGTGGCTG[A/C]GTTGGCAGGTGTGTC	54472
rs202235332	in-del	-/A			intron-variant	TOLLIP	GRCh38.p7	11:1291750	CGTCCTCACCGACCC[-/A]CCTCTGAGGGCACGG	54472
rs207471622	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1307324	CCAGGAGGCACTGGG[C/T]AAGAGGAGATTCTAA	54472
rs367713230	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1292935	TCAGGAGTGACTAGG[A/G]TGAGGAAAACATGGG	54472
rs367871552	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1295031	CCTTTCCCTGCATTT[C/G]TACGAAAGCCTGCGT	54472
rs368059844	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302704	CACGCCAGTCTCCTG[A/G]CACTGGCATGTTCAA	54472
rs368114023	snp	C/T	0.00135821	0.0260242	intron-variant	TOLLIP	GRCh38.p7	11:1288594	CAACATACCCCAATG[C/T]GCCCCACCCCGCCCA	54472
rs368124186	snp	A/G	6.60928e-05	0.00574822	missense, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277116	CTTCCAGCACGGAGC[A/G]GATCACCTCCTGGTC	54472
rs368137609	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276077	TCAGAAAGCTTTTAC[A/G]GGGCCACGCTCGCCA	54472
rs368338912	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299557	ATGATGGAGGAACTA[C/T]TTCAATGGTCACATA	54472
rs368379685	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1294940	TTCCCTGCATTTCTA[C/T]GAAAGCCCGCGTGGC	54472
rs368399346	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275568	CAAAGGATCAAAGGC[C/T]TTTAGGACCCACAGC	54472
rs368436119	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276926	ACAGAAGTCCACGGG[A/G]GGGGGCGACACGGGT	54472
rs368492722	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289664	CTGCTGGTGAGCGGC[A/C]AGACGAGTGCCCAGT	54472
rs368531852	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299641	ATTACTCCCGATACA[C/T]AATGGATATTTTTCT	54472
rs368620685	snp	C/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297899	TAAGCACCTGTTCCT[C/G]TTGGCACACAGGAAA	54472
rs368636975	snp	C/G	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1284503	ACAGGCGCCCACCAC[C/G]GCGCCCGGCTAATTT	54472
rs368698979	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301277	ACTGACATCATTAGC[A/G]ATGGGCTAAATACGT	54472
rs368699497	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1278224	ACAGAGCACAGGCAG[C/T]GTGCGCGGGGCTCGG	54472
rs368708390	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309123	TCTGGAGACCATTGG[C/G]GAGCGGGGCCTGCCT	54472
rs368713777	snp	A/G	1.78159e-05	0.00298457	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277233	CGGGCACCATGCCGG[A/G]GCTACAGACAGCGGG	54472
rs368821055	snp	A/G	0.000190283	0.00975221	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295693	GCCCACTGCGCCTCC[A/G]TACTGCAGCTGCTGG	54472
rs368841341	snp	A/G	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1281968	CTGGCAGTGGCTGCC[A/G]GGAGGATGGGCTGTG	54472
rs368907142	snp	C/T	0.00438332	0.0466095	intron-variant	TOLLIP	GRCh38.p7	11:1280405	TTCATACTTTGTGGA[C/T]GGGCATTCATGTCCT	54472
rs368973742	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275878	CCGGCGGCAAGACAC[C/T]TGAACCACAAACACC	54472
rs369071402	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273878	TGGGCAGCAGAGAGG[A/G]GGCAGACACCCCACC	54472
rs369086687	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1297209	TGCCATGCACACCAG[A/C]AACCCGTACCTGCCT	54472
rs369144854	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1306369	TGCTCCTTCACGGCC[A/C]ATGGGATCTTGCCGT	54472
rs369149324	snp	A/G	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1295805	TACACCTGCGGGGCC[A/G]GGGACCAGAGAGGCC	54472
rs369154559	snp	C/T	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1288130	CCCACAGCCAGGCCT[C/T]GACTTCCTGACCCTG	54472
rs369270898	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1287275	GCGTCTGTTAAAGAC[A/G]TGTCATGAGACATTT	54472
rs369325002	snp	A/G	2.05662e-05	0.00320666	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295720	CTGGGCCGCCTGGGC[A/G]TCCAGCTGGACCTGC	54472
rs369336963	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309662	GGCACCGCCCCACTG[A/C]GCAGGCGCCGCGCCA	54472
rs369389832	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1284371	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	54472
rs369509985	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1282073	CTGCTAGGATAATTA[A/C]AAAATACTTCAAAGG	54472
rs369566335	snp	G/T	0.00676609	0.0577691	intron-variant	TOLLIP	GRCh38.p7	11:1292874	CTGCAGGATCTGGAG[G/T]AAGAGCTGCAGGAAG	54472
rs369619314	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308989	GCCCGCATCCATCTA[A/G]GGGACCATTAGGGTT	54472
rs369629471	snp	C/T	6.42915e-05	0.00566936	intron-variant	TOLLIP	GRCh38.p7	11:1277286	GTTTGGTAAAAACGT[C/T]GGAAAGTTCCAGAAG	54472
rs369695317	snp	C/T	0.000388651	0.0139347	intron-variant	TOLLIP	GRCh38.p7	11:1288604	CAATGCGCCCCACCC[C/T]GCCCAGGCGTGCAGC	54472
rs369750923	snp	A/C			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303138	GGAAGAGTACAGGAC[A/C]GAATGAGAATAAGCA	54472
rs369758521	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291992	AGTTCCCTCCTTTCA[C/T]TTCTAATCAAAGCTG	54472
rs369761966	snp	A/G	9.9553e-05	0.00705454	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290181	CCCCACGGCAGCCAC[A/G]CTCAGCCACGTGCAG	54472
rs369764814	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1282787	AAGTATAATTAAAAT[A/G]AATAAATAAATAAAT	54472
rs369775019	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1296628	GGCCTGGTTGCTGGT[A/G]GAGGCCTGGTTGCTG	54472
rs369775514	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289962	CCCTGTGCGCCCAGC[A/G]GAGGGGACACGTGCA	54472
rs369800147	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311020	AACCGGCAGCCTGGC[C/T]GCTTGCCTGTTTTGA	54472
rs369808375	in-del	-/AG			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273875	GGTTGGGCAGCAGAG[-/AG]GGGGCAGACACCCCA	54472
rs369809819	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291375	AGAGACCCCGGGAGC[C/T]ATCCCGGCCCTCCCA	54472
rs369829607	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300380	CGTACCTTTCCACAC[A/G]AAAGAAAAGAGGTCT	54472
rs369963945	snp	A/G	0.000367273	0.0135463	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290335	TGCCGTGGGCGTCTC[A/G]TACACCGCGTAGCCC	54472
rs369992898	snp	A/G	0.000187436	0.00967898	intron-variant	TOLLIP	GRCh38.p7	11:1286123	GATGGTCCCGGGGTC[A/G]AGGAGGAACATCCAC	54472
rs369996833	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1297391	GCACAAGCCAGTCAG[C/T]GCTCCACAACCAATG	54472
rs369999254	snp	A/G			upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310595	TTTATCTTACATATA[A/G]ACAAGCGTACCCAGG	54472
rs370002766	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1280667	GCGGGCCAGGCTGGG[C/G]AGGCGCCGGACGCCC	54472
rs370008179	snp	A/G	3.34891e-05	0.00409187	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277012	GTGTCCAAAGAGCGG[A/G]GGCAAAACGGCATCG	54472
rs370056014	snp	C/T	0.00438332	0.0466095	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301810	GACCTGGGCTGGGCT[C/T]GTGGCTAAAGGGACA	54472
rs370107634	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1294772	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTTC	54472
rs370160205	snp	A/G	1.75099e-05	0.00295883	intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290456	TGCCAACCATCAGGA[A/G]AGGGTGGGTTCTCTA	54472
rs370173941	snp	C/G	0.00159617	0.0282053	intron-variant	TOLLIP	GRCh38.p7	11:1283696	AATTAGGGATAGGAA[C/G]CAGAAAGAGGTAAGC	54472
rs370184466	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291500	CCAACCCCCCTCTGA[A/G]AGTACTGCCACCCTG	54472
rs370193997	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274868	GACACAGGCGGGGGC[A/G]GGGGAGGGTGGGGGT	54472
rs370240528	snp	A/G	0.000316664	0.012579	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288727	TGCCTCAGGGACTCC[A/G]GGATGGTGATGTGGG	54472
rs370301597	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1285825	CAAACAAAATTCAAA[C/T]GTAAGCCTTGGCTTC	54472
rs370310047	snp	A/G	8.69573e-05	0.00659326	synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277212	CGGCGGCCGGGGGCA[A/G]GGCCACGGGCACCAT	54472
rs370421950	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1281315	TTTATTTTTGTGAAG[C/G]AGATGGTCTGACCTC	54472
rs370518757	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308349	GCTTTCGCCATGTGA[C/T]GTGTAAGCTCCCACT	54472
rs370543921	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1291679	CCTCGCTGACCCCCC[G/T]CTGAGGGCACGGCCG	54472
rs370559443	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274605	AGCCTCCGGCGACCT[C/G]TCTTCTATCTCCGGA	54472
rs370562981	snp	C/G			intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1298059	AGCCCATGCCAGCAG[C/G]CTCTATGACTAGCTC	54472
rs370600804	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297169	CTTAGGCAAAGTGCA[C/T]GTGCTGAGGCCGCCA	54472
rs370752589	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300634	CCCGACACCTGTTAG[A/G]AATACGTTTCCGACT	54472
rs370840264	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308011	TCCAGTACTGGGCTG[C/T]GCGAGGGCAGGGACC	54472
rs370999509	snp	A/G	0.00557542	0.0525036	intron-variant, downstream-variant-500B	TOLLIP, LOC105376512	GRCh38.p7	11:1297706	CATAGGCCAGGGCCC[A/G]GAGGGACCCCCTGCC	54472
rs371085953	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300285	CCTCCCCCATGTGCC[A/G]CTCTCAGAGGATCAC	54472
rs371102731	snp	A/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289654	GAAATCCCACCTGCT[A/G]GTGAGCGGCCAGACG	54472
rs371392619	in-del	-/C			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308869	CATCAGGGTGCGGGA[-/C]CCGCCTCCACCTGGG	54472
rs371574523	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299923	TGGAGACTCGGGGGA[C/T]GGAGGCGGAGGCGGA	54472
rs371584235	snp	A/G	0.000172597	0.0092881	intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1295786	CTGCGGGAGCTCACC[A/G]ATGTACACCTGCGGG	54472
rs371661227	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1295042	ATTTCTACGAAAGCC[C/T]GCGTGGCTCACAGTG	54472
rs371762554	snp	A/C			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289988	GTGCACGCTGTATCC[A/C]TGGGTCATGCTTGTC	54472
rs371815197	snp	A/G	5.55993e-05	0.00527225	intron-variant	TOLLIP	GRCh38.p7	11:1295604	CCACCCCCACCGAGC[A/G]CACCAGCCCCAGGCA	54472
rs371832813	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280369	CCATCCCAGCAGCGG[C/T]GTCCACCTGCGTGTT	54472
rs371924457	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289887	CCAGATCAGTGCCCA[A/G]CGGAGGGGACACGTG	54472
rs371926120	snp	A/G	0.000798403	0.0199641	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299720	CAAGTCTAAATGCCC[A/G]TGTGAAGGCCAACAA	54472
rs371931657	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309212	AGGCCCCCTCCCCCG[C/G]GGCTGCCTCCCCAAA	54472
rs372005060	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1293696	AGGGGGGCCAGAGGC[A/G]TGGGCAACGCCAGGG	54472
rs372125723	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288868	CCCGCCTCGAGTCCC[C/T]GTCTTATCTGTGGAA	54472
rs372163559	snp	C/T	0.000183641	0.00958054	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290340	TGGGCGTCTCGTACA[C/T]CGCGTAGCCCAGGCG	54472
rs372240396	snp	A/T	0.00119737	0.0244387	intron-variant	TOLLIP	GRCh38.p7	11:1306145	GGCCTTTTTGAAACG[A/T]GAGGGAAGCACTGCA	54472
rs372244606	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1305854	TCTCTGACGGCACCG[C/T]GGTGGCTGCAGCGGA	54472
rs372252798	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1291080	GAGGTCCTCGGGGTG[A/G]GAGTGAACGTGTGTT	54472
rs372311105	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306597	AAAGCAGGGCTCCTC[C/T]AGGTGCTAGTAACTG	54472
rs372408377	snp	A/G	0.000162237	0.00900511	intron-variant	TOLLIP	GRCh38.p7	11:1288573	CGGCATAGCCCCGAC[A/G]TGCTCCAACATACCC	54472
rs372408628	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304022	GCCTGGGCTACAGAG[C/T]GAGCCTCCATGTAAA	54472
rs372447607	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1278050	ATGCAATCTATCGAG[C/T]AGGAGACGCACGGCG	54472
rs372485985	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300338	CCATTCCTCCCTCAC[C/T]GACGCCAGAGCTCTA	54472
rs372540291	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1302061	GTCTGAGGGGCTGGC[C/T]CTGCCTTGAAGGCCC	54472
rs372608430	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1296312	GAAGAACGCAGGAAG[G/T]AAATCGATTCCAAAC	54472
rs372617757	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1291713	CGTCCTCGCTGACCC[A/C]CCTCTGAGGGCACGG	54472
rs372802328	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303411	GGCAGCCTCTGCGTG[C/T]CACTGTGTGCCTGAG	54472
rs372869759	snp	C/T	0.00163836	0.0285744	intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290182	CCCACGGCAGCCACG[C/T]TCAGCCACGTGCAGC	54472
rs372933935	snp	C/T	5.12886e-05	0.00506376	missense, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288626	GCGTGCAGCTCACCG[C/T]GTAGGACATGACGAG	54472
rs372939460	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302982	TTAATTATACAAAAC[A/G]CAACAGGCGCTTCAA	54472
rs372968261	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1310197	CCTCCCCGCCGCGCC[C/G]CTCCGCAGGAGCCCC	54472
rs373098181	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309827	TGCGCATGCCCAGTC[A/T]TGACGGTTGTCGGCG	54472
rs373099776	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291565	CCATCCTCACTGACG[C/T]CCCTCTGAGGGCACG	54472
rs373185297	in-del	-/CCT			intron-variant	TOLLIP	GRCh38.p7	11:1284882	CCAGTGCCGTCTCCT[-/CCT]TCCCATCGTCAGGGC	54472
rs373191090	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303184	GACTACAGAACAAGC[A/G]ACTTTAAATGGGGTC	54472
rs373201520	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1283362	CGGCCTGGATGCTGC[A/G]GACTCAGACGGGCTC	54472
rs373210412	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1294490	GCCCGCGTGGCTCAC[A/G]GTGTGTCTCCTTTCC	54472
rs373267419	snp	A/G	7.05293e-05	0.00593799	intron-variant	TOLLIP	GRCh38.p7	11:1288605	AATGCGCCCCACCCC[A/G]CCCAGGCGTGCAGCT	54472
rs373319858	snp	C/T	0.000153988	0.00877327	intron-variant	TOLLIP	GRCh38.p7	11:1285999	GGGAGGGAGCACACG[C/T]ACCTGTGATGGGCAC	54472
rs373439059	snp	C/G	0.00139195	0.0263446	intron-variant	TOLLIP	GRCh38.p7	11:1295818	CCGGGGACCAGAGAG[C/G]CCAGTGAGTCAGGGT	54472
rs373469888	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1285392	CTGGGCCCATCCATG[G/T]TGGGGGCCGGTCTTG	54472
rs373516730	snp	C/G	0.00835141	0.0640778	intron-variant	TOLLIP	GRCh38.p7	11:1293025	CCTACTCTGGCCACG[C/G]TGCAGGGGCTGAGCG	54472
rs373521011	in-del	-/G	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1278467	CAACACCAGCAACAA[-/G]GACCTGCAGGGGTGT	54472
rs373551427	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300870	CACTTCCATGACTGG[A/C]CCCCTGCGGAGCCTT	54472
rs373569115	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1297214	TGCACACCAGAAACC[C/T]GTACCTGCCTGTGCC	54472
rs373630245	snp	A/C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279407	GTCCATCAAGCCCTC[A/C/T]GGGAACGGTGAGCGT	54472
rs373631889	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298209	CATGCACAGCTCTGA[A/G]GACATGGCAGGAAAA	54472
rs373719023	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1287261	GTGTTTGTATGAAAG[C/T]GTCTGTTAAAGACGT	54472
rs373785313	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299901	GGCGGTCCCTGCCGC[A/G]AACACATGGAGACTC	54472
rs373918504	in-del	-/CTCTT	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1297539	GCGTGTGCTCAACCG[-/CTCTT]CTCTAAAAAGCAAAA	54472
rs374029431	snp	A/G	1.67697e-05	0.00289561	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290281	GGGCACCGTGCAGTG[A/G]ATGACCTTATTCCAG	54472
rs374135029	in-del	-/C			intron-variant	TOLLIP	GRCh38.p7	11:1294476	GCATTTCTACGAAAG[-/C]CCGCGTGGCTCACAG	54472
rs374147650	snp	C/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289764	GGGCGGACACATGCA[C/T]GCTCTGTCCCTGGAA	54472
rs374198955	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1302626	CCAGCCTCGGCCTCA[C/T]GCTCCACACCAGCCT	54472
rs374243365	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275980	TGACTGTCATAACCA[A/G]GTGTCACCTAAAATC	54472
rs374335160	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275975	ATTTCTGACTGTCAT[A/T]ACCAGGTGTCACCTA	54472
rs374522426	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1293604	CCACCACTGGAGCTG[C/T]GCCACAGAAGGCTGG	54472
rs374555515	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308924	CCTCCATCTAGGGTG[C/T]CATCAGGGTGCGGGA	54472
rs374558966	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1291716	CCTCGCTGACCCCCC[G/T]CTGAGGGCACGGCCG	54472
rs374561701	in-del	-/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308882	GACCCGCCTCCACCT[-/G]GGGGGGCCATCAGGG	54472
rs374624012	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1306319	CTCTACCCAAGGACA[A/G]AAGAACCCTCCCAGG	54472
rs374648737	snp	C/T	7.10581e-05	0.0059602	missense, synonymous-codon, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277230	CCACGGGCACCATGC[C/T]GGGGCTACAGACAGC	54472
rs374889536	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276299	CGCAGCAGGAGAGAC[A/G]GACGGCAGCCTCCGG	54472
rs374900667	snp	A/G	6.77679e-05	0.0058206	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277192	ACAGCGGGGCTGGGC[A/G]TTCACGGCGGCCGGG	54472
rs374967831	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1306341	CCTCCCAGGACCCCA[C/T]TAGCGGCCCCTCTGC	54472
rs375034388	snp	A/G	0.00318978	0.0398085	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300001	CACCAACTCTGGAGG[A/G]GCATTCAGGAATGGA	54472
rs375043112	snp	G/T	0.000132183	0.0081286	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277117	TTCCAGCACGGAGCG[G/T]ATCACCTCCTGGTCC	54472
rs375082016	snp	C/T	0.000155988	0.00883004	intron-variant	TOLLIP	GRCh38.p7	11:1295798	ACCGATGTACACCTG[C/T]GGGGCCGGGGACCAG	54472
rs375094188	snp	C/G			intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1309280	CAGCGTGGGCGCGTC[C/G]GTCCGGCCCGCCCCG	54472
rs375157686	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1280002	TGTTGCTGCTTCTCA[C/T]TCCACAGAGCGTTAT	54472
rs375247428	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1305208	ACAGACTCACAACCC[A/G]GCCTAAAAAATCCAG	54472
rs375251753	snp	G/T			intron-variant, upstream-variant-2KB	TOLLIP	GRCh38.p7	11:1290737	CTCCTCAGAAGTGGC[G/T]GAGGAGGGAAAGAGG	54472
rs375254926	snp	G/T			upstream-variant-2KB, intron-variant	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1311155	CTTTGGGGGCCTAGG[G/T]ACTTCCCCGGGCCCC	54472
rs375335756	snp	A/G			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1304574	TCTCCGCGTGGATCC[A/G]GAGGTGGCACAGACA	54472
rs375337623	snp	C/T	1.67217e-05	0.00289147	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290385	GGTCCATGCGGGTCA[C/T]GCCGTAATTCTTGGC	54472
rs375415946	snp	A/G/T			intron-variant	TOLLIP	GRCh38.p7	11:1281561	GGGTCTCTGGGCAGC[A/G/T]ATCAGCAGGCGACAG	54472
rs375446535	snp	C/T			intron-variant, upstream-variant-2KB	TOLLIP, LOC105376512	GRCh38.p7	11:1303302	AGATGAAACAAAAGC[C/T]AGTCAAGCAGCAGGC	54472
rs375452637	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276584	AAGGGCGTGAGTTTT[C/T]GTCTGGGAAGTTCTA	54472
rs375469267	snp	A/G	0.00199481	0.0315187	intron-variant	TOLLIP	GRCh38.p7	11:1278562	GCAAGGAAGGCCACC[A/G]CTTCCCGGCTCCTTC	54472
rs375477714	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298256	GCACACATGGCAGAC[A/G]GACAGGCGGCTCGTG	54472
rs375482671	snp	C/T			intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299563	GAGGAACTATTTCAA[C/T]GGTCACATAAAAATA	54472
rs375495025	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291621	TCTGAGGGCACCGCC[A/G]CCCTGTTCTCACCGC	54472
rs375639703	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1296020	CTCACTCAGGAGATC[C/T]CCAAATGCAGGTTTC	54472
rs375659736	snp	C/T	5.37658e-05	0.0051846	intron-variant	TOLLIP	GRCh38.p7	11:1288587	CGTGCTCCAACATAC[C/T]CCAATGCGCCCCACC	54472
rs375663195	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1293462	TCCCACTGGGGCCCC[A/G]GGAGACAACAAGGGG	54472
rs375809794	snp	C/T	0.000368002	0.0135597	intron-variant	TOLLIP	GRCh38.p7	11:1286104	GCAGCTGAAACACAG[C/T]GGAGATGGTCCCGGG	54472
rs375835141	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1286835	TCACTGCACTGCTGT[C/T]GTCTCTGAGTTTAGT	54472
rs375844613	snp	C/T	0.000100219	0.00707809	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1290329	ATTGTGTGCCGTGGG[C/T]GTCTCGTACACCGCG	54472
rs375916147	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1291945	ATCTCTGGACTGCCA[A/G]GTCCTCTGTTTTCTA	54472
rs375938675	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1282508	TAGGAAATTGTTTAG[G/T]AGAAATACCTAATGT	54472
rs376080090	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1280924	GGCCCAGTGGCACCC[A/G]CGCTGGTCTCTCACG	54472
rs376099623	snp	C/G	1.72859e-05	0.00293984	synonymous-codon, missense, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277207	GTTCACGGCGGCCGG[C/G]GGCAGGGCCACGGGC	54472
rs376105942	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289148	GCCACCTGTCAAGCC[C/T]CAGAGCAGCCGGGGT	54472
rs376184285	snp	C/T	0.000112159	0.00748779	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1276843	TGGGAGGGGAGCCCC[C/T]GCCCCGTCCTGGACC	54472
rs376190069	snp	A/G	0.000153988	0.00877328	intron-variant	TOLLIP	GRCh38.p7	11:1288611	CCCCACCCCGCCCAG[A/G]CGTGCAGCTCACCGC	54472
rs376336431	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1274590	GAGGAGAGGAGGGGG[A/G]GCCTCCGGCGACCTG	54472
rs376349045	snp	A/C			intron-variant	TOLLIP	GRCh38.p7	11:1285930	TCTAAGCCCCGTTCC[A/C]TCCTCCCGCACCTGC	54472
rs376358531	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275883	GGCAAGACACTTGAA[A/C]CACAAACACCAGACA	54472
rs376369997	snp	A/C	0.000316381	0.0125734	intron-variant	TOLLIP	GRCh38.p7	11:1286143	GGAACATCCACCCAT[A/C]AGAACCTCGGGAATC	54472
rs376389813	snp	A/G	0.0023933	0.0345097	intron-variant	TOLLIP	GRCh38.p7	11:1281172	AATTTGGTAATCAAA[A/G]TAATACTTTGTTTAA	54472
rs376389910	snp	A/G	6.18028e-05	0.00555856	intron-variant	TOLLIP	GRCh38.p7	11:1285974	GTTTCTACCAGGGGA[A/G]AGGCACCCAGGGAGG	54472
rs376459543	snp	C/T	0.000399281	0.0141238	intron-variant	TOLLIP	GRCh38.p7	11:1285194	GCGCCCTGCCCGCAA[C/T]TTGGCCACTTCCATG	54472
rs376532852	in-del	-/C	0.498632	0.0261223	intron-variant, upstream-variant-2KB	TOLLIP, TOLLIP-AS1	GRCh38.p7	11:1308863	GGGGCCATCAGGGTG[-/C]CGGGACCCGCCTCCA	54472
rs376539979	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291638	CCTGTTCTCACCGCA[C/T]CCCTCTGAGGGCACG	54472
rs376669117	snp	C/T	0.00597247	0.0543191	intron-variant	TOLLIP	GRCh38.p7	11:1286762	CAAAACTGTCCACTG[C/T]GGATAAGTCATTGCA	54472
rs376895247	snp	C/T	0.000798403	0.0199641	intron-variant	TOLLIP	GRCh38.p7	11:1297357	CTCCTCACCTGTGTC[C/T]CCATCTAAGGCCTGG	54472
rs376897582	snp	C/T	0.000116786	0.00764065	utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1277026	GGGGCAAAACGGCAT[C/T]GAGGCAGAGGCTCTA	54472
rs376960196	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1283813	AAGACAGCCACAGAG[C/T]GCCCGGCCCAGAAGT	54472
rs377122220	snp	A/G	3.33806e-05	0.00408524	synonymous-codon, intron-variant, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1288678	GTCCCCCTGCCTCCC[A/G]CTCAGGCTGTACCAC	54472
rs377188815	snp	C/G			intron-variant, upstream-variant-2KB, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1289491	GCCACGGACGGGACT[C/G]AGGACCCTCAAGGGT	54472
rs377302132	in-del	-/TT	0.00318978	0.0398085	intron-variant	TOLLIP	GRCh38.p7	11:1304887	CCATCTAGGCATCTC[-/TT]AACTAGAAAGATGAA	54472
rs377336238	in-del	-/A			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300131	ACTTTTAAAATAAAA[-/A]GGACAGGGTAGGGCT	54472
rs377406606	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1307679	GCTCTGAGTCTCCTG[C/T]TAGGCAGAAAGGAGC	54472
rs377407901	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1291518	TACTGCCACCCTGTC[C/T]TCACCACCCACCCCC	54472
rs377495722	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1279116	CTGCAAAATCGATGA[C/T]GGTGGCTGTGACGCT	54472
rs377585391	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298413	TGGTCACAGGGACGT[A/G]TGGGCGTGGGGTCCA	54472
rs377618446	snp	C/T			intron-variant	TOLLIP	GRCh38.p7	11:1288258	GGCCCAGGGCTGTAT[C/T]TCAGACCCTGGAGGG	54472
rs377619944	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1283303	GAGCAAGATGGGGAC[C/G]CCTCCAGGCCAAGGG	54472
rs377636075	snp	C/T			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1300594	CAACGGAGAGAGCCG[C/T]TGCTTCCTTGGGCCA	54472
rs377664757	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1297608	TTTTGACTGGGACAC[A/G]TCACGAGTGACCTTT	54472
rs377668664	snp	G/T			intron-variant	TOLLIP	GRCh38.p7	11:1280968	CGGGAAATTGAGCAG[G/T]TGGCTGCTGTTGCCA	54472
rs377687186	snp	C/G			intron-variant	TOLLIP	GRCh38.p7	11:1287843	ACCCTCCCCGCCGCA[C/G]CCTCCCTGCCGCACC	54472
rs377719713	snp	A/G			downstream-variant-500B	TOLLIP	GRCh38.p7	11:1273949	CCAGGGTGGCTCGGG[A/G]TCTCTAGAGTGCTGC	54472
rs377736201	snp	A/G			intron-variant	TOLLIP	GRCh38.p7	11:1288171	CCCCCAGGCTTCCCC[A/G]ACATCTCCAGAGATG	54472
rs386749663	multinucleotide-polymorphism	CA/TG			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1301390	CACAAACGGCATCCG[CA/TG]GGCGCCTGCCCACCC	54472
rs397803441	in-del	-/G	0.5	0	intron-variant	TOLLIP	GRCh38.p7	11:1283481	TGCCTGGGCATGGGG[-/G]CTGGGGGCTCCGGTG	54472
rs527242058	snp	C/T	0.00279162	0.0372561	intron-variant	TOLLIP	GRCh38.p7	11:1294379	TTCCCTGCATTTCTA[C/T]GAAAGCCCGCATGGC	54472
rs527243866	snp	A/C	0.00159617	0.0282053	intron-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1299857	GGCACATCCACCCAG[A/C]GCATCGCCACGCGGC	54472
rs527282843	snp	A/G			intron-variant, nc-transcript-variant	TOLLIP, LOC105376512	GRCh38.p7	11:1298539	ACTCTTTAGGTGTCC[A/G]TTAAAGACAGTGGGA	54472
rs527320923	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOLLIP	GRCh38.p7	11:1275241	CCACATGTGCACGCG[C/T]GTGGCAGTCTCACTG	54472

Page 1 | 2