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

WSB2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs10638	snp	A/G	0.488241	0.0757703	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033955	CATAACTGGACTGAA[A/G]ATTTAACGTAAGGCT	55884
rs13649	snp	A/G	0	0	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033658	ATACCAAATGGCTCC[A/G]GGAAAACTGTCCTGC	55884
rs4128857	snp	A/G	0.318656	0.240388	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063760	AATAAGTGCCAACTG[A/G]TATTTCTCACGTTGG	55884
rs4128858	snp	C/T	0.456803	0.140473	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063793	ATCATCCTTACTAGG[C/T]AAAATGTATTATGAT	55884
rs4131122	snp	C/G	0.329084	0.237162	intron-variant	WSB2	GRCh38.p7	12:118059383	AGACTTCTGTTGGTC[C/G]GGGCTGGCCTAGAGG	55884
rs4767655	snp	A/C	0.356169	0.226336	intron-variant	WSB2	GRCh38.p7	12:118055717	CCTCCTGGGTTCAAG[A/C]AATTCTTATGCCTCA	55884
rs4767656	snp	C/T	0.460813	0.134379	intron-variant	WSB2	GRCh38.p7	12:118057313	agagtctcactctgc[C/T]gcccaggctggagtg	55884
rs5745897	snp	A/G	0.00199481	0.0315187	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032318	CCCCTTAAGGACAGC[A/G]GCAAAGTATGAAGCT	55884
rs5745898	snp	G/T	0.0360663	0.129354	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032333	GGCAAAGTATGAAGC[G/T]AAATATCTGATGGCC	55884
rs5745899	snp	C/T	0.0154538	0.0865337	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032386	AGGCTCAGCATCTGC[C/T]GTACCTGGAACTTCA	55884
rs5745900	snp	C/T	0.00795532	0.062565	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032491	ttttttgaggcaaga[C/T]catgctctgtcagtc	55884
rs5801265	in-del	-/A	0.325799	0.238232	intron-variant	WSB2	GRCh38.p7	12:118053601	GCACACCATCTTGTG[-/A]AAGAGTAGGCACCAG	55884
rs6144890	in-del	-/ACATT	0.488905	0.0736498	intron-variant	WSB2	GRCh38.p7	12:118059220	AAAAAAAAATCTAAA[-/ACATT]ACATTACAATTTATT	55884
rs7134751	snp	C/T	0.369142	0.219784	intron-variant	WSB2	GRCh38.p7	12:118057350	cgccatctcggctca[C/T]tgcaacctccgcccc	55884
rs7135150	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118049801	CAGCATGCAGAGTAC[C/G]CATCTCAACAAACTC	55884
rs7136393	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118052683	ACTCCTCACTGCTGG[G/T]TAACCATGACTCACA	55884
rs7300357	snp	C/T	0.0520825	0.152737	intron-variant	WSB2	GRCh38.p7	12:118055062	ATATTTTTATATATA[C/T]GGTCTGAGTAAATAG	55884
rs7300973	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118048289	CTCAGAATACTGTTC[A/T]TCAAAATATGTGATT	55884
rs7306158	snp	A/G	0.0663309	0.169604	intron-variant	WSB2	GRCh38.p7	12:118050085	catgcctgtaatccc[A/G]gctactcaggaggct	55884
rs7310726	snp	G/T	0.143959	0.226396	intron-variant	WSB2	GRCh38.p7	12:118054841	AAGCCTTTGTAAAGA[G/T]ACTATTCATTCTCAG	55884
rs7312586	snp	A/G	0.425277	0.178263	intron-variant	WSB2	GRCh38.p7	12:118043069	TGAGTGGGGCAGGGA[A/G]GCGACATAGTCAGAA	55884
rs7484385	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061377	AAGACGCGCGAACCA[G/T]ATAAAAATGGGGCAG	55884
rs7484410	snp	C/G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061446	ACGGGATAAAACCCA[C/G/T]GGGTTGTGCGGGGTC	55884
rs7485457	snp	A/C	0.0722614	0.17581	intron-variant	WSB2	GRCh38.p7	12:118056076	CTGCTCTCCCGGCTT[A/C]CCCTCTAGCCCCGCA	55884
rs7485548	snp	A/G	0.198324	0.244601	intron-variant	WSB2	GRCh38.p7	12:118051201	acagacaataacaac[A/G]gctggatgtagagaa	55884
rs7486055	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118055047	AAAAAAGAAAGAAAT[A/C]TATTTTTATATATAT	55884
rs7487673	snp	A/G	0	0	intron-variant	WSB2	GRCh38.p7	12:118054000	agtatttttttctca[A/G]ttatacatgatgata	55884
rs7488835	snp	A/C	0.270351	0.24917	intron-variant	WSB2	GRCh38.p7	12:118051376	acatgaaaacaaccc[A/C]atgtccatcaactga	55884
rs7963217	snp	C/G/T	0.0659589	0.169201	intron-variant	WSB2	GRCh38.p7	12:118051749	gaggccgaggtgggt[C/G/T]aatcacttgaggtca	55884
rs7967764	snp	A/G	0.49975	0.0111793	intron-variant	WSB2	GRCh38.p7	12:118043729	TGGGATTACTGGCAT[A/G]AGCCACCCCACCCGG	55884
rs9788041	snp	C/T	0.433675	0.169598	synonymous-codon	WSB2	GRCh38.p7	12:118035249	AAGGTACAAGCCTTC[C/T]GGAGAGAAGCACACA	55884
rs9888438	snp	A/G	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118054747	TAGGAAAATAATAAC[A/G]TAGGTATATCTTGTT	55884
rs10558297	in-del	-/TATT			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032697	CTAAGTTTTTTTGGC[-/TATT]TATTTATTTATTTTT	55884
rs10624358	in-del	-/TC			intron-variant	WSB2	GRCh38.p7	12:118034583	AAAGCGCTCTCTCTG[-/TC]TCTCTCTCTCGGCAC	55884
rs10774977	snp	A/G	0.489142	0.0728777	intron-variant	WSB2	GRCh38.p7	12:118058993	GAGCCACCCCGGCGC[A/G]TTTGGTTGATATTTT	55884
rs10850952	snp	G/T	0.482008	0.0931261	intron-variant	WSB2	GRCh38.p7	12:118040273	GTGGGGCAGCGCCTG[G/T]CAGCTGGGAACCAAC	55884
rs11068778	snp	A/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118037668	AGCGAAACTCTGTCT[A/T]AAAAAAAAAAAAAAG	55884
rs11068779	snp	C/T	0.284471	0.247612	intron-variant	WSB2	GRCh38.p7	12:118038162	TGCAGGTGGTGGCCA[C/T]GGCCCACCAGCATGC	55884
rs11068780	snp	C/T	0.29341	0.246202	intron-variant	WSB2	GRCh38.p7	12:118038274	GAATTAAAGCAATAA[C/T]GCTGGAGACTCACCG	55884
rs11068781	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039790	gttctgttgcctagg[C/T]gggagtgcaatggca	55884
rs11068782	snp	A/G	0.0887219	0.191022	intron-variant	WSB2	GRCh38.p7	12:118040487	CACTGCCagccgagc[A/G]tggtacctcatacct	55884
rs11068783	snp	A/G	0.0603597	0.1629	intron-variant	WSB2	GRCh38.p7	12:118041937	tttttgtatttttta[A/G]tagagatggggtttg	55884
rs11068784	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045117	TGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	55884
rs11068785	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118045118	GCGGTGGCTCATGCT[A/T]GTAATCCCAGCACTT	55884
rs11068786	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118045141	CAGCACTTTGGGAGG[C/G]CAAGGTGGGCAGATC	55884
rs11068787	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046879	agggctcgagcagtc[C/T]ttccatctcagcctc	55884
rs11068788	snp	A/G	0.347253	0.230308	intron-variant	WSB2	GRCh38.p7	12:118047635	GGAGGATCACTTGAG[A/G]CAAGGAGTTCAAGGC	55884
rs11068790	snp	C/T	0.35574	0.226537	intron-variant	WSB2	GRCh38.p7	12:118054339	gaggttacagtgagc[C/T]gagatcgtgccactg	55884
rs11068791	snp	A/T	0.330714	0.236612	intron-variant	WSB2	GRCh38.p7	12:118054684	CTCTGTCTCAAAAAA[A/T]AATAATAATAATAAT	55884
rs11068792	snp	C/T	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118054825	GTTAATAAATCATAT[C/T]AAGCCTTTGTAAAGA	55884
rs11068793	snp	A/C	0.0614824	0.164198	intron-variant	WSB2	GRCh38.p7	12:118057080	TAAAAGAAGAACAAA[A/C]CCAGTGACTCCTGTC	55884
rs11068794	snp	A/G	0.339203	0.233544	intron-variant	WSB2	GRCh38.p7	12:118057495	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	55884
rs11068795	snp	A/C	0.48955	0.071525	intron-variant	WSB2	GRCh38.p7	12:118057938	tttttttttttttaa[A/C]ttaaatttttagtag	55884
rs11068796	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058368	TTTTATTTTTTTTGA[A/G]ACAGGGTCTTGCTCT	55884
rs11068797	snp	C/T	0.378372	0.214524	intron-variant	WSB2	GRCh38.p7	12:118058416	GCAGTAGCACCATCA[C/T]GGCTCACTGCAACCT	55884
rs11068798	snp	A/G	0.489083	0.0730708	intron-variant	WSB2	GRCh38.p7	12:118058494	GCTGGGACTACAGGC[A/G]CATTCTACCATGCAC	55884
rs11068799	snp	G/T	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118059685	GATTGCTTTCAGATT[G/T]AACTGTAAGGAGGCA	55884
rs11308776	in-del	-/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118055924	CTGTTTTTTTTTTTT[-/T]AAATCTCCCAAACCA	55884
rs11426565	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118055016	AAAAAAAAAAAAAAA[-/A]GAAAAAAGAAAGAAA	55884
rs11540133	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033244	GCTGTTTAACTTCAT[G/T]GGATTAATCAGCTGG	55884
rs11540134	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033309	AATTGTGTAAAGAAT[G/T]GGTGTAGTCATGACT	55884
rs11540135	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033198	GAAACAAAAATAGCT[C/T]CTTAAAAGTACTGTT	55884
rs11550988	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063773	TACCAGTTGGCACTT[A/T]TTGCATCATAATACA	55884
rs11613209	snp	A/C	0.019353	0.0964467	intron-variant	WSB2	GRCh38.p7	12:118054216	GTCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA	55884
rs11832085	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118051589	agacaaagtagatta[C/G]tggttgcctggagag	55884
rs12228444	snp	A/G	0.000905611	0.0212599	synonymous-codon	WSB2	GRCh38.p7	12:118034246	TCTTGGGGATTGGCA[A/G]TGCTAGGACTTGGTA	55884
rs12229137	snp	C/T	0.161924	0.233971	intron-variant	WSB2	GRCh38.p7	12:118046355	ATAGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG	55884
rs12300828	snp	C/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118039143	AGACTGTCACCCTCC[C/T]AGCCTTGCCAGGATG	55884
rs12302795	snp	C/G	0.423257	0.180228	intron-variant	WSB2	GRCh38.p7	12:118040438	ATGGTGGCAAGCTGC[C/G]TCAGTACACACATTA	55884
rs12309202	snp	C/T	0.0944967	0.195752	intron-variant	WSB2	GRCh38.p7	12:118039293	CTCCAGCTCTTGCTT[C/T]AAAAATAAAAAAGCC	55884
rs12310685	snp	A/G	0.488424	0.0751925	intron-variant	WSB2	GRCh38.p7	12:118044115	CGAAGGCAAAACTCT[A/G]TCTCAAAAAAAAAAA	55884
rs12311489	snp	C/T	0.00396038	0.0443227	intron-variant	WSB2	GRCh38.p7	12:118048261	TCAATAAGCCTCATA[C/T]TGCAAACATTTCCTC	55884
rs12313999	snp	G/T	0.279195	0.248289	intron-variant	WSB2	GRCh38.p7	12:118039377	AGTTGGAATTAGAGA[G/T]AGATTTTCCATGGGG	55884
rs12319850	snp	C/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118034826	GAGAAAATGGGACAC[C/T]GTTATTAGCAAAATC	55884
rs12320789	snp	G/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118046396	tgagcccaggaggca[G/T]aggttgcagtgaacc	55884
rs12578639	snp	A/T	0.299411	0.245069	intron-variant	WSB2	GRCh38.p7	12:118051831	ATACAAAACTTAGCC[A/T]GGCGTGGTGGTGTGT	55884
rs12579444	snp	C/T	0.28052	0.24813	intron-variant	WSB2	GRCh38.p7	12:118058731	gatggagtttcactc[C/T]tgttgcccaggctgg	55884
rs12582265	snp	A/G	0.195837	0.244062	intron-variant	WSB2	GRCh38.p7	12:118044547	AACTGATGGTAACCC[A/G]CACAAGGATCAAACA	55884
rs12582327	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118051639	ctaaattaaggggta[C/T]agggtttctttctga	55884
rs12818975	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061313	TCGGGGAGGCGGTAC[G/T]CTGACGGGATAAAAG	55884
rs12819129	snp	G/T			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061392	GATAAAAATGGGGCA[G/T]GGGTGGGGGGAGCTG	55884
rs12823138	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049115	TCATATAGTAAATTT[A/G]CTTACATGTCAAGTC	55884
rs12828248	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118049113	ATTCATATAGTAAAT[A/T]TACTTACATGTCAAG	55884
rs12830847	snp	G/T	0.320814	0.239761	intron-variant	WSB2	GRCh38.p7	12:118039980	CGAACTCCTGACCTC[G/T]AGTGATCCGCCCGCC	55884
rs12833894	snp	A/C	0.33303	0.235809	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062721	GGTTACACTCCTGTT[A/C]ACCCCGCTTGGCCGG	55884
rs16948110	snp	G/T	0.1128	0.208988	utr-variant-3-prime, intron-variant	WSB2, RFC5	GRCh38.p7	12:118032917	CAAAAGCTTTTAACT[G/T]TTGTTTTTTTCTTTT	55884
rs33933604	in-del	-/TC			intron-variant	WSB2	GRCh38.p7	12:118034584	TCTSTSTCTCTCTCT[-/TC]CGGCACAGCCCTTTC	55884
rs34253698	snp	A/G	0.00848367	0.0645745	synonymous-codon	WSB2	GRCh38.p7	12:118036433	AGAGTCGGGGGAGAA[A/G]TCACAAGAGACAACA	55884
rs34549466	snp	C/T	0.000527209	0.0162273	missense	WSB2	GRCh38.p7	12:118035290	AGCTAATGTGGACGT[C/T]ACTGTCATCCATGGC	55884
rs34606067	snp	C/T	0.375	0.216506	intron-variant	WSB2	GRCh38.p7	12:118043026	GGGCACGAGGTGTGC[C/T]TGCCACGGCCACACC	55884
rs34646347	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118043477	GAGTGGAGGGAAGGG[-/G]TCTGTCACCCAAGCT	55884
rs34818152	in-del	-/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032373	TCAAACCACCCAGAG[-/G]CTCAGCATCTGCTGT	55884
rs34947187	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118045001	TACCACCATTACTTT[-/T]GCACCAACCCAATAT	55884
rs35299550	in-del	-/A/AA/AG			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033564	AAAAAAAAAAAAAAA[-/A/AA/AG]GCCAGTAATAGTGTC	55884
rs35369829	in-del	-/C			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063668	AATTTCTCCCAACCT[-/C]CCCCCCACCACATCT	55884
rs35426707	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053933	TTACATTTTGACCTC[A/G]CTGAAATCAGGATGT	55884
rs35499134	in-del	-/TTT			downstream-variant-500B, cds-indel, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032714	TTTATTTATTTATTT[-/TTT]AAATAAAGATTGGGT	55884
rs35749330	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118047124	CTACTTTATTCCAAA[-/A]GAATTAAGGCATATT	55884
rs36027266	in-del	-/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063428	GTGATGGAGGCTCCG[-/T]TCTGGAGGAAAAAAA	55884
rs55816764	snp	A/G	0.0941369	0.195465	intron-variant	WSB2	GRCh38.p7	12:118050771	CTGAAAAGATGCTCG[A/G]CCAGGTGTGGTGGCT	55884
rs55973710	snp	A/G	0.261884	0.249717	intron-variant	WSB2	GRCh38.p7	12:118041713	CTGGAGGAATTGAAA[A/G]ATGGCATTGCAATAA	55884
rs55982995	snp	C/T	0.0490535	0.14873	intron-variant	WSB2	GRCh38.p7	12:118053073	CCAGATCTTTTGCTA[C/T]AGTCTCCTGATCAGT	55884
rs56234244	snp	C/T	0.0490535	0.14873	intron-variant	WSB2	GRCh38.p7	12:118052835	CAAAATAGCAAGGCC[C/T]TCCAATGCATTTCAG	55884
rs56270657	snp	A/C	0.0832709	0.186283	intron-variant	WSB2	GRCh38.p7	12:118053096	TGATCAGTCTTCCTA[A/C]CCCTAGAGATGCTGC	55884
rs56882977	snp	C/G	0.338976	0.23363	intron-variant	WSB2	GRCh38.p7	12:118034583	CAAAGCGCTCTCTCT[C/G]TCTCTCTCTCGGCAC	55884
rs57072102	in-del	-/AATAAT			intron-variant	WSB2	GRCh38.p7	12:118054709	AATAATAATAATAAT[-/AATAAT]TCTAGTATATGCATT	55884
rs57072278	snp	C/G	0.0551013	0.156571	intron-variant	WSB2	GRCh38.p7	12:118053862	GGCTGTTACCAGATA[C/G]ATATTCATTTTTAAA	55884
rs57151947	snp	A/T	0.488965	0.0734569	intron-variant	WSB2	GRCh38.p7	12:118057921	ACCACCACACTCAGC[A/T]TTTTTTTTTTTTTTA	55884
rs57272444	in-del	-/TC/TCTCTCTC	0	0	intron-variant	WSB2	GRCh38.p7	12:118034593	CTCTGTCTCTCTCTC[-/TC/TCTCTCTC]GGCACAGCCCTTTCT	55884
rs57353139	snp	A/C	0.357664	0.225629	intron-variant	WSB2	GRCh38.p7	12:118056902	CAAGACTCTGTCCCC[A/C]AAAAATAAAAAATAA	55884
rs57427658	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118059204	TAGCACAAAAAAAAA[-/A]TCTAAAACATTACAT	55884
rs57493385	snp	C/T	0.300926	0.244758	intron-variant	WSB2	GRCh38.p7	12:118050849	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	55884
rs57540760	in-del	-/A	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118046467	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	55884
rs58116528	snp	C/T	0.348134	0.229934	intron-variant	WSB2	GRCh38.p7	12:118047959	TAAGAGACAGTGTCT[C/T]ACTGTTGCCCAGGCT	55884
rs58279660	in-del	-/T	0.448963	0.151372	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062737	ACCCCGCTTGGCCGG[-/T]TTTTTTTTTTCTTTT	55884
rs58436126	snp	C/T	0.27278	0.24896	intron-variant	WSB2	GRCh38.p7	12:118049230	AGAAGAAACTGAAAA[C/T]TCTGATTAAAAACAC	55884
rs58639682	snp	G/T	0.198014	0.244535	intron-variant	WSB2	GRCh38.p7	12:118052616	ACTTAAATGACCCAG[G/T]GCAATAACAGCAGCC	55884
rs58685107	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044018	CAGCTACTTAGGAGG[C/T]TGAGGCAGGAGAATC	55884
rs58958096	snp	G/T	0.030278	0.119257	intron-variant	WSB2	GRCh38.p7	12:118048929	CACCCACAGTGCCCT[G/T]AGGGAGATGCAAGCC	55884
rs58978542	in-del	-/TTACA			intron-variant	WSB2	GRCh38.p7	12:118059228	ATCTAAAACATTACA[-/TTACA]ATTTATTTGATTACA	55884
rs59151662	snp	C/T	0.0607341	0.163335	intron-variant	WSB2	GRCh38.p7	12:118047344	GAAAAGCAGGGAGGT[C/T]GTACCGTGGGAAAGA	55884
rs59196766	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118041907	CTACAGGCGCCCACC[A/C]CCACGCCCAGCTCAT	55884
rs59271270	snp	G/T	0.0509478	0.151255	intron-variant	WSB2	GRCh38.p7	12:118043494	CTGTCACCCAAGCTG[G/T]CGTACAGTGACACAA	55884
rs59687507	snp	C/T	0.0836354	0.186609	intron-variant	WSB2	GRCh38.p7	12:118052703	CATGACTCACAGTAA[C/T]CTTTGTGCCCATGAA	55884
rs59767459	in-del	-/AAA			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063452	AAAAAAAAAAAAAAA[-/AAA]CAAAAAAGGCGGGGC	55884
rs60129426	snp	A/G	0.030278	0.119257	intron-variant	WSB2	GRCh38.p7	12:118058630	CTGCTGGGCCACTGC[A/G]CCTGGCACCATTCAC	55884
rs60260780	snp	C/T	0.0622301	0.165053	intron-variant	WSB2	GRCh38.p7	12:118041899	AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC	55884
rs60389743	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118057935	ATTTTTTTTTTTTTT[-/T]AAATTAAATTTTTAG	55884
rs60432513	snp	A/G	0.0923359	0.194016	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061581	GGGCTCAGGGGAAAA[A/G]GGGGTGTTGGAGAGT	55884
rs60495286	snp	C/T	0.0836354	0.186609	intron-variant	WSB2	GRCh38.p7	12:118054427	TGTAATCCCAGCACT[C/T]TGTGAGGCCAAGGCG	55884
rs60550237	snp	A/G	0.347694	0.230122	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061689	TGTGGGGGTAAGGGG[A/G]ACCAAAGGGGCTGAA	55884
rs60706138	snp	A/C	0.0490535	0.14873	intron-variant	WSB2	GRCh38.p7	12:118053235	TCTGCCCCAGCCCAT[A/C]GGTCCAACCTCCTTC	55884
rs60777883	snp	A/T	0.199873	0.244923	intron-variant	WSB2	GRCh38.p7	12:118057162	ATTAGTGCAGAACTT[A/T]AAAACAAAACAAACA	55884
rs61091236	snp	A/G	0.0225045	0.103662	intron-variant	WSB2	GRCh38.p7	12:118059160	AGTCAGAATTCAGAT[A/G]GGCTGTAAGTAAAAA	55884
rs61094951	snp	A/G	0.301681	0.2446	intron-variant	WSB2	GRCh38.p7	12:118048836	AAAAAAATTGTTATT[A/G]TTTTCATTTACTGAT	55884
rs61421772	in-del	-/AA			intron-variant	WSB2	GRCh38.p7	12:118054241	AAAAAAAAAAAAAAA[-/AA]TTAGCCAGACATGGT	55884
rs61943488	snp	C/T	0.0217236	0.101931	intron-variant	WSB2	GRCh38.p7	12:118034659	GAAGAGTGCCACCTA[C/T]TGAATTATAGATGTT	55884
rs71069403	in-del	-/CCTTCCTGTGTCCCGT	0	0	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062694	CTTCCTGTGTCCCGT[-/CCTTCCTGTGTCCCGT]TTGGCCTCCTGGGTT	55884
rs71099102	in-del	-/T	0.43555	0.167544	intron-variant	WSB2	GRCh38.p7	12:118057776	GTTTTTTTTTTTTTT[-/T]GAGACCCAGGCTGGG	55884
rs71450252	in-del	-/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118039793	TGTTGCCTAGGTGGG[-/G]AGTGCAATGGCATGA	55884
rs71452628	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118043684	ACTCCTGAGCTCAAG[C/T]GATCTGCCCACCTTG	55884
rs71452629	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118062029	GGCAGGGTGAAAACC[A/G]GAGTGGGGGTGGGAA	55884
rs73217914	snp	C/G	0.0225045	0.103662	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033585	TAATAGTGTCTGGAT[C/G]GGTCAGGAGCACGGC	55884
rs73410742	snp	C/G	0.030278	0.119257	intron-variant	WSB2	GRCh38.p7	12:118036212	GTCTCAAAAGAGACC[C/G]ACTGTGCCTTTTTAT	55884
rs73410744	snp	G/T	0.485731	0.0832509	intron-variant	WSB2	GRCh38.p7	12:118036893	CCACTTAAAAATAAA[G/T]GTCAGCGGCCAGGCA	55884
rs73410750	snp	G/T	0.0356815	0.128715	intron-variant	WSB2	GRCh38.p7	12:118046780	GTTTTATTTATTTTG[G/T]TTTTTTTTAAAGACA	55884
rs73410755	snp	A/G	0.0279526	0.114869	intron-variant	WSB2	GRCh38.p7	12:118057871	TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCTGTG	55884
rs73410763	snp	C/T	0.0414363	0.137845	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062597	TAACTGAGGTTCCCG[C/T]GTTCTTTTTCACCAT	55884
rs74489012	snp	C/G	0.146314	0.227484	intron-variant	WSB2	GRCh38.p7	12:118044034	TGAGGCAGGAGAATC[C/G]CTTGAACCCAGTGGG	55884
rs74521854	snp	A/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118045717	CACTGTCTCAAAGAA[A/G]AAAAAAAAAAAAAGG	55884
rs74596198	snp	C/G	0.0221141	0.102801	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032427	GAAATGTAAACGTTG[C/G]CCAATCCATTCCCAG	55884
rs74803373	snp	C/T	0.112983	0.209108	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062252	GAGGCTTTTCATGCC[C/T]GAAAGACCCCATTTC	55884
rs74815768	snp	A/T	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118050180	ACAGAGCGAGACTCC[A/T]TCTCAAAAGAAAAAA	55884
rs74855911	snp	A/G	0.0178098	0.0926698	intron-variant	WSB2	GRCh38.p7	12:118058512	TTCTACCATGCACGC[A/G]CCTATAGTTCGGTAT	55884
rs75024859	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054588	GGCAGGAGAATCGCT[C/T]GAACCCGGGAGGCGG	55884
rs75092807	snp	A/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118050190	ACTCCATCTCAAAAG[A/G]AAAAAAAAGAAACTA	55884
rs75094309	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051907	TGAACCCAGGAGGCA[A/G]AGGTTGTAGTGAGCC	55884
rs75356056	snp	G/T	0.200801	0.245111	intron-variant	WSB2	GRCh38.p7	12:118060282	GAGGTATATCCAATA[G/T]CCTCTGACTTCCACG	55884
rs75436645	snp	C/T	0.0577344	0.159793	intron-variant	WSB2	GRCh38.p7	12:118045790	ACAGTCATCATGCCA[C/T]ACAATAGATCTTCTG	55884
rs75495835	snp	A/G	0.00795532	0.062565	intron-variant	WSB2	GRCh38.p7	12:118057685	CATTACCATATATGC[A/G]TTACCTCACATACTT	55884
rs75689617	snp	A/C	0.0865458	0.189163	intron-variant	WSB2	GRCh38.p7	12:118036837	TGCCAATAGGGTAGT[A/C]GTATGTGCTGATGAA	55884
rs75692718	snp	A/G	0.0456336	0.143994	intron-variant	WSB2	GRCh38.p7	12:118049835	TCAACATTCCCTCTT[A/G]TCAAGGCAAGTTTCA	55884
rs75734538	snp	C/T	0.0103295	0.0711199	intron-variant	WSB2	GRCh38.p7	12:118040340	TGGCCTACTCCATCC[C/T]GCCCACTCTTGGTCA	55884
rs75791403	snp	A/C	0.0589646	0.161423	intron-variant	WSB2	GRCh38.p7	12:118034617	CCTTTCTAAATCTGA[A/C]CACAGTTAGTTCAAA	55884
rs75808300	snp	A/G	0.207559	0.246371	intron-variant	WSB2	GRCh38.p7	12:118060297	TCCTCTGACTTCCAC[A/G]CTGTCTTCTGATGGG	55884
rs75879516	snp	C/T	0.104504	0.2033	intron-variant	WSB2	GRCh38.p7	12:118052802	CAGGAATATGCTAGA[C/T]GGTGCTGATTATGGG	55884
rs75905224	snp	A/G	0.0111196	0.0737302	intron-variant	WSB2	GRCh38.p7	12:118058988	GACGTGAGCCACCCC[A/G]GCGCATTTGGTTGAT	55884
rs75981097	snp	A/G	0.0611083	0.163768	intron-variant	WSB2	GRCh38.p7	12:118042590	ATAAGTAGATATACA[A/G]TATATCTTCGATATT	55884
rs76333372	snp	A/G	0	0	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033562	TAAAAAAAAAAAAAA[A/G]AAGCCAGTAATAGTG	55884
rs76419610	snp	C/G	0.00428376	0.0460818	intron-variant	WSB2	GRCh38.p7	12:118035188	CACTTGTTCTGAGGC[C/G]ATGTAAAGAGAGTTC	55884
rs76456222	snp	A/G	0.0456336	0.143994	intron-variant	WSB2	GRCh38.p7	12:118049819	TCTCAACAAACTCCT[A/G]TCAACATTCCCTCTT	55884
rs76486180	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118053133	TGAAATACCCACACA[C/T]CACATCATTTCTTTC	55884
rs76491900	snp	A/G	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118042724	AAGGCTCCTTAAGGG[A/G]CAATCACAGAAAAAA	55884
rs76540921	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118054583	GCTGAGGCAGGAGAA[G/T]CGCTTGAACCCGGGA	55884
rs77105984	snp	C/T	0.0349115	0.127424	intron-variant	WSB2	GRCh38.p7	12:118042414	GCCCACGACAAAGGG[C/T]TATCCAGCCCAAAAT	55884
rs77268631	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118034594	CTCTGTCTCTCTCTC[G/T]GCACAGCCCTTTCTA	55884
rs77274262	snp	C/T	0.00438332	0.0466095	intron-variant	WSB2	GRCh38.p7	12:118048509	GAGGACCACTTGAAT[C/T]CAGGAGGCAGAGGTT	55884
rs77294308	snp	A/G	0.0154538	0.0865337	intron-variant	WSB2	GRCh38.p7	12:118059356	TTTTAAATTACATAC[A/G]TGGCTCACATTAGAC	55884
rs77339760	snp	C/T	0.198014	0.244535	intron-variant	WSB2	GRCh38.p7	12:118036682	TTTAAATAAGGCAAC[C/T]GGTCTGGATTCTTGA	55884
rs77485549	snp	A/G	0	0	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063438	GCTCCGTCTGGAGGA[A/G]AAAAAAAAAAAAAAA	55884
rs77531942	snp	A/G	0.00448764	0.0471559	synonymous-codon, upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062151	AAACCTGCTCTCCCT[A/G]TCTACCCGCATAGCC	55884
rs77542352	snp	A/G/T	0.0170251	0.090679	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033979	TAAGGCTCTGTTGCC[A/G/T]TGCAAGTGGAATCTC	55884
rs77563909	snp	C/G	0.0955749	0.196603	intron-variant	WSB2	GRCh38.p7	12:118037951	GAGGGATTCAAATTT[C/G]ATGGTTCAAAGGAAA	55884
rs77739770	snp	A/G	0.0130921	0.0798413	intron-variant	WSB2	GRCh38.p7	12:118053424	TCACAACTAAGAAGC[A/G]TACCCTGATCTCACA	55884
rs77946506	snp	G/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118049419	AGATTTTTTTTTTTT[G/T]GAGATGGAATCTCGC	55884
rs78080789	snp	A/G	0.0607341	0.163335	intron-variant	WSB2	GRCh38.p7	12:118044169	ACTGGCCATGGCTCA[A/G]TCTATTTGCAACAGC	55884
rs78282389	snp	A/C	0.0433465	0.140692	intron-variant	WSB2	GRCh38.p7	12:118051565	TGTCTAGAATAGGCC[A/C]ATCTAGAGAGACAAA	55884
rs78454468	snp	A/G	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118040420	TGCATGGACCTTCCT[A/G]AGATGGTGGCAAGCT	55884
rs78502481	snp	A/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118054243	AAAAAAAAAAAAAAT[A/T]AGCCAGACATGGTGG	55884
rs78635633	snp	A/G	0.0236746	0.106192	intron-variant	WSB2	GRCh38.p7	12:118055027	CTTTAAAAAAAAAAA[A/G]AAAGAAAAAAGAAAG	55884
rs78825740	snp	A/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118040671	AAAAAAAAAAAAAAA[A/G]AGGCACTGCCTTGGA	55884
rs79091085	snp	C/T	0.00993419	0.0697739	intron-variant	WSB2	GRCh38.p7	12:118040192	AATAAAGGTCAATCA[C/T]GGTTTCTTCAGCTGT	55884
rs79113900	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118042421	ACAAAGGGTTATCCA[C/G]CCCAAAATATCCATA	55884
rs79168588	snp	C/T	0.0569829	0.158885	intron-variant	WSB2	GRCh38.p7	12:118046657	CCCCTGAGTTTGTTG[C/T]CACGAGAAGCAGCAC	55884
rs79232756	snp	C/T	0.201418	0.245234	intron-variant	WSB2	GRCh38.p7	12:118053912	TAAGACACATCTTTA[C/T]ATATCTTACATTTTG	55884
rs79240959	snp	C/T	0.199564	0.24486	intron-variant	WSB2	GRCh38.p7	12:118056391	AGAACTCTTCTGACC[C/T]CTAGTCAATCTCCTT	55884
rs79381352	snp	C/T	0.0633504	0.166319	intron-variant	WSB2	GRCh38.p7	12:118034890	TTAAAGCTTTCCTCA[C/T]AGGCAAGAAAATTCT	55884
rs79644006	snp	A/G	0	0	intron-variant	WSB2	GRCh38.p7	12:118040670	AAAAAAAAAAAAAAA[A/G]GAGGCACTGCCTTGG	55884
rs79870436	snp	A/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118045716	ACACTGTCTCAAAGA[A/G]AAAAAAAAAAAAAAG	55884
rs79950936	snp	A/G	0.0894459	0.191631	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061469	GCGGGGTCCTGAGGG[A/G]AACCAGCGCCGGATA	55884
rs80079700	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118056088	CTTCCCCTCTAGCCC[C/T]GCACCATCGGTTCTC	55884
rs80091626	snp	C/G	0.199564	0.24486	intron-variant	WSB2	GRCh38.p7	12:118056350	TCTACTCTTATTCAG[C/G]TCTGGCTCAAATGAC	55884
rs80122919	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118055923	TCTGTTTTTTTTTTT[-/TT]AAATCTCCCAAACCA	55884
rs80166352	snp	A/C	0.5	0	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063455	AAAAAAAAAAAAAAA[A/C]AAAAAAGGCGGGGCT	55884
rs80173055	snp	A/G	0.030278	0.119257	intron-variant	WSB2	GRCh38.p7	12:118037214	AGAAGTGAAATCTGC[A/G]GCCACCCCACAAAGT	55884
rs80198634	snp	C/T	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118048854	TTCATTTACTGATAC[C/T]AGTAATTAAAGTAAA	55884
rs111281422	snp	A/C	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118051112	CATAGCCATCAAGGA[A/C]ATGCAAATCGAAACC	55884
rs111330303	in-del	-/A	0.0948562	0.196037	intron-variant	WSB2	GRCh38.p7	12:118037949	AGAGGGATTCAAATT[-/A]TGATGGTTCAAAGGA	55884
rs111332602	snp	A/C	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118046665	TTTGTTGTCACGAGA[A/C]GCAGCACTTAAGAGG	55884
rs111337671	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118058110	GAATGGAAAGGTATA[C/T]ATTATAAGCCTCTTC	55884
rs111444077	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118052929	ACTCGCCTGCATCCT[C/T]CCCATCATCAAGGCT	55884
rs111518457	snp	A/G	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118054907	GTCTAGGCCAGGCAC[A/G]GTGGCTCACGCCTAT	55884
rs111723052	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118058804	CCAGTTCAAGCGGTT[C/T]TCCTGCCTCAGCCTC	55884
rs111860506	snp	A/C	0.0275645	0.114116	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061694	GGGTAAGGGGAACCA[A/C]AGGGGCTGAAGCGAA	55884
rs111918718	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118050496	AAATTTAAAAGTTGG[C/T]TGGGCATGGTGGCGC	55884
rs111983474	snp	C/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118059046	GTATTTATTGTCTGT[C/T]TCTTTCTGAACCCAC	55884
rs111998638	in-del	-/A	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118048582	GAGCAAGACTCTCTC[-/A]AAAAAAAAAAAAAAA	55884
rs112124316	snp	G/T	0.0115144	0.0749975	intron-variant	WSB2	GRCh38.p7	12:118036034	TGGTGAAACCCCATC[G/T]CTAATAAAAATACAA	55884
rs112227765	in-del	-/AC	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118034619	TTTCTAAATCTGACC[-/AC]AGTTAGTTCAAAAGT	55884
rs112272891	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118048030	TTCCTGGGTGCAGGT[G/T]ATCCTCCCATCTCAG	55884
rs112313151	snp	C/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118043526	CATGGCTCACTGCAG[C/G]CTCGACCTCCCTGTT	55884
rs112415267	in-del	-/T	0.298398	0.245271	intron-variant	WSB2	GRCh38.p7	12:118058700	GATATTTTCTTCTTC[-/T]TTTTTTTTTTTTTGA	55884
rs112510763	snp	C/T	0.267364	0.249396	intron-variant	WSB2	GRCh38.p7	12:118036989	GAGTTCAAGACCAGC[C/T]TGGTCAACATGGCAA	55884
rs112535980	snp	C/T	0.0287284	0.116357	intron-variant	WSB2	GRCh38.p7	12:118049105	AATTTATAATTCATA[C/T]AGTAAATTTACTTAC	55884
rs112890460	snp	C/T	0.030665	0.119967	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061450	GATAAAACCCAGGGG[C/T]TGTGCGGGGTCCTGA	55884
rs112919112	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118050631	ACAACAGAGCAAGAC[C/T]CTCTCTCTCTCTCAA	55884
rs113012207	snp	A/G	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118045775	ACATTATTAATAACC[A/G]CAGTCATCATGCCAT	55884
rs113338121	snp	A/C	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118049775	CACAAATTTATCCCC[A/C]TCAACTCTAGCAGCA	55884
rs113350351	snp	C/T	0.00761606	0.0612375	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043202	CCAGGCAAGAGACAT[C/T]GGGCACTTGGGGGTG	55884
rs113836288	in-del	-/T	0.5	0	intron-variant	WSB2	GRCh38.p7	12:118057920	ACCACCACACTCAGC[-/T]ATTTTTTTTTTTTTT	55884
rs114125609	snp	A/G	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118047350	CAGGGAGGTCGTACC[A/G]TGGGAAAGAGCTGAT	55884
rs114174660	snp	A/G	0.0150606	0.0854603	intron-variant	WSB2	GRCh38.p7	12:118040122	AGGCTACAATAAGCC[A/G]AGATCGCAGCATTGC	55884
rs114185419	snp	C/T	0.0150606	0.0854603	intron-variant	WSB2	GRCh38.p7	12:118040692	CTGCCTTGGAGAAGC[C/T]GTCCTGATCAGCAGC	55884
rs114259095	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056957	TGCTTATGCCAAACA[C/T]TTCACATGAAATGCT	55884
rs114370612	snp	A/G	0.0456336	0.143994	intron-variant	WSB2	GRCh38.p7	12:118049934	GCCTCAAGGGCAAGG[A/G]CCATGTCTGATTTAT	55884
rs114659592	snp	G/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118039346	ATAAATGGTGGTATA[G/T]CTACCCCATTAATGC	55884
rs114800227	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118044406	TTCCCTTATCACTAG[C/T]TTAGAAATCCCCAAG	55884
rs114803709	snp	C/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118038182	CACCAGCATGCCTTC[C/T]ATTGGGGTGGATTTG	55884
rs114833616	snp	C/T	0.0134861	0.0810011	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063652	ATGATAACCTCAGAA[C/T]TAATTTCTCCCAACC	55884
rs114879825	snp	C/T	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118043783	AAACAAGCTGGCCTT[C/T]GGTGAAATCTGCTGT	55884
rs115670279	snp	A/C	0.00676609	0.0577691	intron-variant	WSB2	GRCh38.p7	12:118053856	GACCCTGGCTGTTAC[A/C]AGATAGATATTCATT	55884
rs115684937	snp	C/T	0.0142736	0.0832652	intron-variant	WSB2	GRCh38.p7	12:118034734	ATGCATCATCTCAAT[C/T]TTATTCTCCCTTGTG	55884
rs115747678	snp	C/T	0.0178098	0.0926698	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032726	TTTTTTAAATAAAGA[C/T]TGGGTCTTATCTCAC	55884
rs115911603	snp	C/T	0.0111891	0.0739551	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042916	AACTGCCACTGGGTG[C/T]GAAGCTCAGATCTCT	55884
rs116310525	snp	C/T	0.0433465	0.140692	intron-variant	WSB2	GRCh38.p7	12:118051121	CAAGGAAATGCAAAT[C/T]GAAACCACTATGAAA	55884
rs116319493	snp	A/C	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118041620	CCCTCCTTCCAATCC[A/C]TCCAGCCCCTGATCC	55884
rs116646014	snp	C/G	0.0154538	0.0865337	intron-variant	WSB2	GRCh38.p7	12:118058122	ATATATTATAAGCCT[C/G]TTCTAGGCAAAGCAG	55884
rs116971725	snp	C/T	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118043642	TTGTAGGACGGAGTT[C/T]TGTCATGTTGCCCAG	55884
rs117266864	snp	A/G	0.00478085	0.0486577	intron-variant	WSB2	GRCh38.p7	12:118040153	ACTCCAGCCCATGCA[A/G]CACAGTGAGACTCTG	55884
rs117394766	snp	C/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118059261	CATGTAGCAGGAATA[C/T]TTTAGACATGTTGTA	55884
rs117570803	snp	C/G/T	0.00146986	0.02707	intron-variant	WSB2	GRCh38.p7	12:118034377	AAATGAAACAGAAAC[C/G/T]GATGCTAAGACAGAG	55884
rs117882038	snp	A/T	0.00897284	0.066377	missense	WSB2	GRCh38.p7	12:118035062	CAAATGCAATGGGAG[A/T]TTTCAGTTCCAGGGC	55884
rs118101112	snp	C/T	0.0165278	0.0893908	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061692	GGGGGTAAGGGGAAC[C/T]AAAGGGGCTGAAGCG	55884
rs118135632	snp	C/G	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118056164	CTAGCTCCTCACCCT[C/G]CCCTCAAAATCCAGC	55884
rs137858243	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118042672	GTATAGTATTATCTT[G/T]GGGGCGGGCAGGGGC	55884
rs137937049	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118055700	GCTCACTGCAACCTC[A/G]GCCTCCTGGGTTCAA	55884
rs137991542	snp	C/T	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118046394	CTTGAGCCCAGGAGG[C/T]AGAGGTTGCAGTGAA	55884
rs138098757	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040864	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCTGTC	55884
rs138163811	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054205	GGTGAAACCATGTCT[C/T]TACTAAAAATCCAAA	55884
rs138250029	snp	C/T	0.00874735	0.0655527	intron-variant	WSB2	GRCh38.p7	12:118056245	ACACATTGCCCTTCT[C/T]TCTACCCTCTGCCAA	55884
rs138362565	in-del	-/AATAATAATAAT			intron-variant	WSB2	GRCh38.p7	12:118054682	AACTCTGTCTCAAAA[-/AATAATAATAAT]AATAATAATAATAAT	55884
rs138366120	in-del	-/CGTCCTTCCTGTGTCC	0.459233	0.136827	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062675	TATGAGCCCTGGGTA[-/CGTCCTTCCTGTGTCC]CGTCCTTCCTGTGTC	55884
rs138412526	snp	A/G	0.0205511	0.0992634	intron-variant	WSB2	GRCh38.p7	12:118036582	CGGAGGGAGGGAAAG[A/G]TACCACCACCAAATC	55884
rs138563153	snp	C/T	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118053512	TTTCTCTCTGCCCCC[C/T]GCCCTCGTCATCAGT	55884
rs138639406	snp	A/G	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118045581	CAGGGACCTGGTGGC[A/G]CATGCCTGTAATCCC	55884
rs138737831	snp	A/G	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118037001	AGCTTGGTCAACATG[A/G]CAAAACCCCATCTCT	55884
rs138748807	snp	C/T	0.0126979	0.078662	intron-variant	WSB2	GRCh38.p7	12:118054441	TTTGTGAGGCCAAGG[C/T]GGGCAGATCACCTGA	55884
rs138971577	snp	G/T	0.000741406	0.0192394	synonymous-codon	WSB2	GRCh38.p7	12:118035009	AATGACTCCACCATG[G/T]GGAAAAAATGTGCAG	55884
rs138986796	snp	A/G	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061535	GGAAACCGGGAAAAG[A/G]GGAGCGATAGAAACC	55884
rs139061277	snp	A/G	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118037722	CCAAACCACAAAAAT[A/G]AATGATGAACCACCT	55884
rs139226769	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062258	TTTCATGCCTGAAAG[A/G]CCCCATTTCTTAGTT	55884
rs139297732	snp	C/T	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118048462	GAGTGTGGTGGCACA[C/T]GCCTGTAATCCCAGT	55884
rs139707510	snp	A/G	0.00755907	0.0610114	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064153	ATTTGGGCATGGATC[A/G]TCTTAAAGAAGCCCG	55884
rs139786952	snp	A/G	0.000149697	0.0086502	intron-variant	WSB2	GRCh38.p7	12:118034936	TTAAAAAGCTCCATG[A/G]TATACTCAGCAGAAA	55884
rs139873567	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118037540	AGGCGTGGTGTAGCA[C/T]GCCTATAATCCCAGC	55884
rs139990136	snp	A/G	0.180383	0.240111	intron-variant	WSB2	GRCh38.p7	12:118037593	GAATCGCTTGAACCC[A/G]GGAAGCGGAGGTTGC	55884
rs140009270	snp	C/G	0.0138799	0.0821421	intron-variant	WSB2	GRCh38.p7	12:118052820	TGCTGATTATGGGGC[C/G]AAAATAGCAAGGCCT	55884
rs140068044	snp	C/G	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118056566	AGTGAGTAAATATTT[C/G]TCTAATAAATACATA	55884
rs140175692	snp	C/T	3.29527e-05	0.00405898	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042884	AGTCTTATCCCGTGA[C/T]GCGGAGACCAAAATC	55884
rs140319130	in-del	-/AA	0.499992	0.00199679	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063437	GGCTCCGTCTGGAGG[-/AA]AAAAAAAAAAAAAAA	55884
rs140348648	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118046672	TCACGAGAAGCAGCA[C/T]TTAAGAGGCAGGCTA	55884
rs140529258	in-del	-/TTTA			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032699	AAGTTTTTTTGGCTA[-/TTTA]TTTATTTATTTTTTA	55884
rs140555955	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118036095	TAGTCCTAGCTACTC[A/G]GGAGGCTCAGGCAGC	55884
rs140815709	snp	G/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118058617	TTGGCCTCCCAAACT[G/T]CTGGGCCACTGCGCC	55884
rs140869577	snp	C/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118047593	GTTGGCAGGGTGTGG[C/T]GGCTACGCCTTTAGG	55884
rs140958597	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043843	TGATGTAGGCCAGGC[A/G]TGGTGGCTCATGCCC	55884
rs141032879	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118037683	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG	55884
rs141090224	snp	C/T	0.031825	0.122064	intron-variant	WSB2	GRCh38.p7	12:118054538	AGCCGGGCTTGGTGG[C/T]GCATGCCTGTAATCC	55884
rs141091370	snp	C/T	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118045425	GGGAGGGGCCGGGCA[C/T]GGTGGCTCACACCTG	55884
rs141172203	snp	A/G	3.29554e-05	0.00405914	synonymous-codon	WSB2	GRCh38.p7	12:118035231	GTCATCTGCCACCGT[A/G]GCAAGGTACAAGCCT	55884
rs141259738	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118049464	TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG	55884
rs141279657	snp	A/G	1.7704e-05	0.00297518	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043356	GCTACTTCGGCTTTT[A/G]GCTTCAAACCCTTTA	55884
rs141381417	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118034004	AATCTCTTCCTCTAA[A/G]ACTGACTTTCACATG	55884
rs141641701	snp	A/G	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118042600	ATACAATATATCTTC[A/G]ATATTAAAATAGCCT	55884
rs141679574	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050510	GCTGGGCATGGTGGC[A/G]CGCCTGTAGTATCAG	55884
rs141751040	snp	A/C/T	0.0131122	0.0800881	intron-variant	WSB2	GRCh38.p7	12:118046113	TTCACACTGTGACAG[A/C/T]GGAGTTCAACAGTCA	55884
rs142026288	snp	C/G	0.123452	0.215605	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061342	AGCTGAGGGGTTGCT[C/G]AGGGGAAACGGGGGC	55884
rs142029014	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061905	GGGAGGACGTAAGAA[A/T]TGGGGGGTGCGGCGA	55884
rs142325762	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036798	CATGTGCAGAGACTT[C/G]TGAGTCTGCTTCTGA	55884
rs142357330	in-del	-/C			intron-variant	WSB2	GRCh38.p7	12:118052516	CAAACACACACCCCC[-/C]TTGCTCCCTGACCAC	55884
rs142525009	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041490	CAAGTTTTCAGGCTC[A/C]TTGCTAAAAGAGCAG	55884
rs142701119	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118051467	GTATATGCTAGAATA[C/T]GGATGAACTGTGAAA	55884
rs142866164	snp	C/T	0.000281921	0.0118693	intron-variant	WSB2	GRCh38.p7	12:118052499	GCAGGAGACAACATG[C/T]TTCAAACACACACCC	55884
rs143188824	snp	G/T	0.00284672	0.0376199	synonymous-codon	WSB2	GRCh38.p7	12:118035222	TCGTTACCTGTCATC[G/T]GCCACCGTGGCAAGG	55884
rs143542122	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118050374	CTAAACTTGGCCAAG[C/T]GCCATGGCTCACACC	55884
rs143606734	snp	A/G	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118053236	CTGCCCCAGCCCATC[A/G]GTCCAACCTCCTTCC	55884
rs143663620	snp	A/G	0.0150606	0.0854603	intron-variant	WSB2	GRCh38.p7	12:118044208	GGGGTGACCTGCCTT[A/G]TGGGATAACTAAATA	55884
rs143802874	snp	C/T	0.00478085	0.0486577	intron-variant	WSB2	GRCh38.p7	12:118060722	TTTTAGGGCTTGGTG[C/T]CCCCCGCCCCGAGTC	55884
rs144088396	snp	G/T	0.00795532	0.062565	intron-variant	WSB2	GRCh38.p7	12:118046709	GAGGTTTAAGACAGC[G/T]TGGAACCACCAGTTA	55884
rs144108882	snp	C/T	0.141596	0.225274	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063207	TTTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA	55884
rs144429637	snp	G/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118058653	CCATTCACTTTCCTT[G/T]AACCATTTGATTTTC	55884
rs144500748	snp	C/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118042397	TTAGAATGCACAGGA[C/G]AGCCCACGACAAAGG	55884
rs144645720	snp	C/G	0.0134861	0.0810011	intron-variant	WSB2	GRCh38.p7	12:118037126	GGTGGAGGTTGCAGT[C/G]ACCTGAGATCACGTC	55884
rs144676365	snp	A/G	0.00478085	0.0486577	intron-variant	WSB2	GRCh38.p7	12:118043973	AAAAAAAAACAATTC[A/G]CCGGGCGTAGTGGCG	55884
rs144854804	snp	A/G	1.64814e-05	0.00287061	synonymous-codon	WSB2	GRCh38.p7	12:118035074	GAGTTTTCAGTTCCA[A/G]GGCCCAGATCCTGAG	55884
rs144930037	snp	C/G	0.0134861	0.0810011	intron-variant	WSB2	GRCh38.p7	12:118045525	CAATATGGTGAAACC[C/G]CATCTCTACTAAAAA	55884
rs145072233	snp	A/G	1.64901e-05	0.00287137	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052443	CAAACTGGTGGGGGC[A/G]CCCGGGCTTGAGTTC	55884
rs145093422	snp	A/G	0.000148276	0.00860907	synonymous-codon	WSB2	GRCh38.p7	12:118034343	TGTCCAGAACTGGAC[A/G]TGGCCATCTCTTGTC	55884
rs145096561	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061515	GGGAGGTGAACAGAG[C/G]TGAGGGAAACCGGGA	55884
rs145374747	snp	A/G	0.199564	0.24486	intron-variant	WSB2	GRCh38.p7	12:118055885	CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTAAAC	55884
rs145573797	snp	A/G	0.0205511	0.0992634	intron-variant	WSB2	GRCh38.p7	12:118038597	GAATATGATATTCTA[A/G]TTCCCCACGGAAACC	55884
rs145664213	snp	A/G	0.000181206	0.00951683	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042887	CTTATCCCGTGACGC[A/G]GAGACCAAAATCAAA	55884
rs145761893	snp	A/G	0.0205511	0.0992634	intron-variant	WSB2	GRCh38.p7	12:118043988	GCCGGGCGTAGTGGC[A/G]GGTGCCTGTAACCCC	55884
rs145786929	in-del	-/A	0.26326	0.249648			GRCh38.p7	12:118048583	GAGCAAGACTCTCTC[-/A]AAAAAAAAAAAAAAT	55884
rs145867861	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118038039	ATTTAAAAAGCAATT[A/G]TTTTCCCATTTTATA	55884
rs145960461	snp	A/C	0.0123036	0.0774623	intron-variant	WSB2	GRCh38.p7	12:118037419	CGCCTGCAATCCCAG[A/C]ACTTTGGGAGGCCCA	55884
rs145994764	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041635	CTCCAGCCCCTGATC[C/G]TCTTCATGACCCTTT	55884
rs146081023	snp	A/G	0.0134861	0.0810011	intron-variant	WSB2	GRCh38.p7	12:118056548	TCCTGGTGGAGGGCA[A/G]GCAGTGAGTAAATAT	55884
rs146092737	snp	C/T	0.00953873	0.0683987	intron-variant	WSB2	GRCh38.p7	12:118052561	GCCACTGTCTCCCTG[C/T]GGCAAAGAGCCACAC	55884
rs146098590	in-del	-/A/T			intron-variant	WSB2	GRCh38.p7	12:118037666	AGCGAAACTCTGTCT[-/A/T]TAAAAAAAAAAAAAA	55884
rs146239199	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053996	AGGTAGTATTTTTTT[C/T]TCAGTTATACATGAT	55884
rs146334925	snp	C/G	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062253	AGGCTTTTCATGCCT[C/G]AAAGACCCCATTTCT	55884
rs146455688	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118034618	CTTTCTAAATCTGAC[C/T]ACAGTTAGTTCAAAA	55884
rs146545770	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118049450	TCTGTTACCCAGGCT[A/G]GAGTGCAGTGGCGCG	55884
rs146625430	snp	G/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118035650	TTATAGGACTGCCTA[G/T]TATTTGCTTCATAAA	55884
rs146762379	snp	C/T	0.00478085	0.0486577	intron-variant	WSB2	GRCh38.p7	12:118049654	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	55884
rs146969934	snp	A/C	0.02016	0.0983543	intron-variant	WSB2	GRCh38.p7	12:118058990	CGTGAGCCACCCCGG[A/C]GCATTTGGTTGATAT	55884
rs147050380	snp	A/G	4.94336e-05	0.00497135	synonymous-codon	WSB2	GRCh38.p7	12:118036427	CAGGGCAGAGTCGGG[A/G]GAGAAGTCACAAGAG	55884
rs147184268	snp	A/G	0.000988158	0.0222059	synonymous-codon	WSB2	GRCh38.p7	12:118036424	AAGCAGGGCAGAGTC[A/G]GGGGAGAAGTCACAA	55884
rs147211979	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118032868	TAAAAGGGGACTTTT[G/T]TTTTTCTTAATGGAA	55884
rs147319000	snp	A/G	0.00755907	0.0610114	intron-variant	WSB2	GRCh38.p7	12:118051578	CCAATCTAGAGAGAC[A/G]AAGTAGATTAGTGGT	55884
rs147327624	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118047363	CCGTGGGAAAGAGCT[A/G]ATGAGGCAAGACAGA	55884
rs147490130	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118057953	ATTAAATTTTTAGTA[A/G]AGATGGGGGTCTGGC	55884
rs147728932	snp	A/G	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118038640	TTCAACACAATCTAT[A/G]AGATCAGTAAGGGTG	55884
rs147753824	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118035502	AAGGGTATCTCAGAA[A/G]GCTCCAGGTGTCCTG	55884
rs147823738	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063862	TCTTGTGTTTTCCTG[C/T]GGCAATTATGGGGCT	55884
rs148022824	snp	A/G	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118037139	GTGACCTGAGATCAC[A/G]TCACTGCACTCCAGC	55884
rs148041083	snp	C/T	0.0433465	0.140692	intron-variant	WSB2	GRCh38.p7	12:118050419	CTTGGGAGGCTGAGG[C/T]GGGAGGATTTCTTGA	55884
rs148170944	snp	G/T	0.123452	0.215605	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061338	TAAAAGCTGAGGGGT[G/T]GCTCAGGGGAAACGG	55884
rs148182603	in-del	-/G	0.157642	0.232314	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061825	GCCGAGAAGAAACCT[-/G]GGGAGAGCTGGGCTT	55884
rs148390736	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118042494	GGGGCAATTCACCCC[A/G]AGAGGGTACAAACTA	55884
rs148518097	snp	A/G	0.0225045	0.103662	intron-variant	WSB2	GRCh38.p7	12:118057400	CTGCCTCAGCCTCCC[A/G]AGTAGCTAGAATTAC	55884
rs148572352	snp	C/T	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118051864	CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC	55884
rs148687165	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063261	GGCCGATATGGCCAA[A/T]CCCAATCTCTACTAA	55884
rs148695294	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	WSB2, RFC5	GRCh38.p7	12:118032919	AAAGCTTTTAACTGT[C/T]GTTTTTTTCTTTTCT	55884
rs148974093	snp	A/T	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118038463	ACGGGAGAACTGGGG[A/T]GGTAACAGCCCCCAG	55884
rs149035616	snp	C/G	0.0205511	0.0992634	intron-variant	WSB2	GRCh38.p7	12:118060345	ATAGAGGCAAGGTCC[C/G]CACCCATCAGTGTAT	55884
rs149214065	snp	C/G	0.180064	0.240019	intron-variant	WSB2	GRCh38.p7	12:118036007	AGGAGTTTGAGACTA[C/G]CCTGGCCAACATGGT	55884
rs149322428	snp	A/G	0.00795532	0.062565	intron-variant	WSB2	GRCh38.p7	12:118037062	TGGTGCACGCCTGTA[A/G]GCCCAGCTATTTGGG	55884
rs149493367	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118046660	CTGAGTTTGTTGTCA[C/T]GAGAAGCAGCACTTA	55884
rs149740454	snp	C/T	0.000153988	0.00877328	synonymous-codon	WSB2	GRCh38.p7	12:118036502	GGACCTCATGCTCCA[C/T]AGAAAGACCTGTGGA	55884
rs149841002	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118037795	CAGCAAGTGACTCAA[C/T]GCAACACAAAATTCA	55884
rs149901700	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118034615	GCCCTTTCTAAATCT[A/G]ACCACAGTTAGTTCA	55884
rs149969035	snp	A/G	0.201418	0.245234	intron-variant	WSB2	GRCh38.p7	12:118054141	CTTTGGGAGGCCAAG[A/G]CAGGCAGATCACTTG	55884
rs150016816	snp	C/T	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118048998	GTGACAGAAAAAAGA[C/T]ATATTTATCTATACA	55884
rs150072011	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118041771	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTTGC	55884
rs150124134	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050577	CCAGCAGGTTGAGGC[C/T]GCAGTGAGCCGTGAC	55884
rs150363405	snp	C/T	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118040617	AATACGAAAATTAGC[C/T]AGGCATGGTGGCACA	55884
rs150617123	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055799	TTTGTATTTTTAGTA[A/G]AGACAGGTTTTTGCT	55884
rs150713183	snp	A/G	0.0205511	0.0992634	intron-variant	WSB2	GRCh38.p7	12:118037645	TGCACTCCAGCTTGG[A/G]CAACAACAGCGAAAC	55884
rs150766658	snp	G/T	0.000625906	0.0176794	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034192	GCACAAGATGTGGTG[G/T]TGCTTAAAAAGTCCT	55884
rs150895939	snp	A/G	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118042678	TATTATCTTTGGGGC[A/G]GGCAGGGGCGATTAG	55884
rs150915813	snp	C/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118056193	GCATAATCTGAACTT[C/G]CCTGGGCTTGTACTT	55884
rs151011671	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058397	CTGTTGCCCAGGCTG[C/G]AATGCAGTAGCACCA	55884
rs151045353	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044252	GGAGTCACATGCTTG[C/G]TCAGAAAGTTCTCTC	55884
rs151264861	snp	A/C	0.0162398	0.0886349	intron-variant	WSB2	GRCh38.p7	12:118048100	CCAGGCTAATTTTTA[A/C]AACTTTTTTGTAGAA	55884
rs151297944	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118036076	GCCTGGTGGCGCACG[C/G]TTGTAGTCCTAGCTA	55884
rs180956807	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033168	TGATTAGATAACTAC[A/G]TGCCACTGAAGGAGA	55884
rs180986627	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063567	TCAATTTACTAACCA[A/G]GTCTCAATCAAGATC	55884
rs181037480	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118043435	CAGTCTATCAACTTT[C/T]CATCCTGGGACACGT	55884
rs181216666	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062438	TTCAAGTCACTCTCC[C/T]GCCTCTCATTCCTTT	55884
rs181248693	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042639	ACACAGTATATGTTC[A/G]GTATTAAACTCTATT	55884
rs181357119	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045872	TCCCTCTCCCACCCC[C/T]GGTAACCACCATTCT	55884
rs181697142	snp	C/T	0.029116	0.117091	intron-variant	WSB2	GRCh38.p7	12:118045296	CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG	55884
rs181741311	snp	C/T	0.00874735	0.0655527	intron-variant	WSB2	GRCh38.p7	12:118039011	TAGCAGAGAATGTTC[C/T]TTTTAGGCTCCCCAA	55884
rs181849713	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118056704	CCAGGAGTTCAAGAC[C/T]AGCCTGGCCAACGTG	55884
rs181860920	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057107	TGTCTCTTGGAGTCT[A/G]GGCCCAAACTAAACT	55884
rs181946603	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033940	TCAACACTTGCTGTT[C/G]ATAACTGGACTGAAA	55884
rs181947644	snp	C/G	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118051945	CGCCATTGCACTCCA[C/G]CCTAGGAGACAGAGG	55884
rs182086362	snp	C/T	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118039668	TAATTGTTATACGCC[C/T]GTACATGGTCATATA	55884
rs182178608	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118042169	AAACCTGATGCCCCA[C/T]AGCCTGAGAGAATTA	55884
rs182347379	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118047778	ATAGTAGCGAAACAT[C/G]GGAGAAATGTGAAAA	55884
rs182415433	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035538	GAAGGGTTACTAACA[C/T]TTCCTTGTGCTAATT	55884
rs182485877	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060552	TATCCCATTTTGCAG[A/G]TCAAAACTGAGACGT	55884
rs182507094	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044607	ACAGGGCTGTGTAGA[A/G]GTATCCTGTCCTGGA	55884
rs182693275	snp	C/T	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118040198	GGTCAATCATGGTTT[C/T]TTCAGCTGTCAAATC	55884
rs182694886	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118057209	GGGGTGGGGTATCTA[G/T]CTTCAACTGGTATGG	55884
rs182960021	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034781	TGGCATGACTTACAG[A/G]TCTTTAATTACATTT	55884
rs183000724	snp	A/G	0.00676609	0.0577691	intron-variant	WSB2	GRCh38.p7	12:118048463	AGTGTGGTGGCACAC[A/G]CCTGTAATCCCAGTT	55884
rs183048002	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049208	GCATTATCATTAAAC[C/T]GACCACAGAAGAAAC	55884
rs183266018	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053288	ACACTCTGGCCACAA[A/T]ATCTCCTTGACATGC	55884
rs183298163	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058511	ATTCTACCATGCACG[C/T]GCCTATAGTTCGGTA	55884
rs183301802	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118049981	CCTAACTCAGTGTTA[C/T]GCAAAGAAACTATGT	55884
rs183394637	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054610	GGGAGGCGGAAGGCA[A/G]AGGTTGCGGTGAGCT	55884
rs183404329	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036592	GAAAGGTACCACCAC[C/T]AAATCTGCAGGCCCT	55884
rs183520638	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037929	TTTGAATGGGAAATC[C/T]GAATTAGAGGGATTC	55884
rs183522155	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056453	CTATCACCATTTGAT[C/T]GCCATCTGTCTCCCC	55884
rs183542798	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040893	TCTCTACTAAAAATA[C/G]AAAACATTAGCCAGG	55884
rs183875808	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118040581	GCCTGACCTTCATGG[C/T]AAAACCCCGTCTCTA	55884
rs183886474	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118043980	AACAATTCGCCGGGC[A/G]TAGTGGCGGGTGCCT	55884
rs184015223	snp	A/C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041173	ACTAAATGTGCCCCC[A/C/G]ACACATAAAGCCCTA	55884
rs184019484	snp	G/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118058891	AGTAGAGACGGAGTT[G/T]CATTATGTTGGTGAG	55884
rs184113269	snp	C/T	0.00953873	0.0683987	intron-variant	WSB2	GRCh38.p7	12:118045319	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC	55884
rs184302573	snp	C/T	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118045180	AGGAGATCGAGACCA[C/T]GGTGAAACCCCTTCT	55884
rs184670959	snp	A/C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037262	GCATTTTACACCCCC[A/C/G]ACCTTGTGTATGGAA	55884
rs184797363	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055317	CACTCTACAGCGCAC[A/G]GGACAGCCCCCAGCA	55884
rs184930673	snp	G/T	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118050542	TACTTGGGAGGCTAG[G/T]GCAGGAGGATAGCTT	55884
rs185058768	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032566	TCCATGTCCCAGGCT[C/T]GAGCAGTTCTCCCAC	55884
rs185153855	snp	C/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118040325	AAAAGCTCTCATAAT[C/T]GGCCTACTCCATCCC	55884
rs185159266	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057885	CGCCTCAGCCTCCTG[G/T]GTATCGGGCTACGGG	55884
rs185466918	snp	C/T	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118041648	TCCTCTTCATGACCC[C/T]TTACCACTGCCTCCT	55884
rs185628400	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118059491	CAACTGTTGCCCATT[G/T]TATTTCCTTTACAAT	55884
rs185710912	snp	A/G	0.000454679	0.0150709	intron-variant	WSB2	GRCh38.p7	12:118052281	GTTTGGAAATGCGCC[A/G]GATGGGGCCCCAGTA	55884
rs185717888	snp	A/G	0.0607341	0.163335	intron-variant	WSB2	GRCh38.p7	12:118045272	GGAGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC	55884
rs185877243	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118063029	TGTCCAGGCTCCCCC[C/T]TCCCATTTTTCTCTT	55884
rs185885493	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042687	TGGGGCGGGCAGGGG[C/T]GATTAGGAAAAAACT	55884
rs185891569	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046400	CCCAGGAGGCAGAGG[C/T]TGCAGTGAACCGAGG	55884
rs186025696	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043794	CCTTCGGTGAAATCT[A/G]CTGTGACTTTTCTTT	55884
rs186145451	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063705	GTAAATAATGGAGAA[A/G]GAGCTGCTTATTTTT	55884
rs186192951	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118051400	CAACTGATAAATGTA[A/C]GAACAAAATTTGGCA	55884
rs186203065	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033597	GATCGGTCAGGAGCA[C/T]GGCCTCTGAGTCCCC	55884
rs186282677	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039749	TTTCTTTTTTATTTT[G/T]TTTTATTTTTTTGAG	55884
rs186436240	snp	C/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118048218	ACAGGCGTGAGCCAC[C/T]GCACCCGGCCATATA	55884
rs186449120	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118056808	CGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAC	55884
rs186481709	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053299	ACAAAATCTCCTTGA[C/T]ATGCAAGGGGCTTAT	55884
rs186538987	snp	G/T	1.6574e-05	0.00287867	intron-variant	WSB2	GRCh38.p7	12:118034397	CTAAGACAGAGCTTG[G/T]ATGTTCATGTTTTCA	55884
rs186614285	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041274	GAATGGGATTAGTGC[C/T]CTTAGAAGAAGAGAC	55884
rs186646314	snp	C/T	0.00478085	0.0486577	intron-variant	WSB2	GRCh38.p7	12:118058903	GTTTCATTATGTTGG[C/T]GAGGCTGGTCTCGAA	55884
rs186884643	snp	G/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118035545	TACTAACACTTCCTT[G/T]TGCTAATTTGCTTAT	55884
rs186886281	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118054307	GAAGCAGGAGAAGCA[C/T]TTGAACCCAGGAGGC	55884
rs187038684	snp	A/G	0.0182019	0.0936463	intron-variant	WSB2	GRCh38.p7	12:118057132	TAAACTTGGCTACAC[A/G]GAGAGAAAGCCCTAA	55884
rs187111780	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118044877	ATGAGAAAGCTGAAC[A/G]CCAGGATGAGGTCAG	55884
rs187226001	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118044075	AGTGAACCAAGACCG[C/T]ACCATTGCACTCCAG	55884
rs187608611	snp	C/G	0.0138799	0.0821421	intron-variant	WSB2	GRCh38.p7	12:118045223	CAAAAAATTAGCCGG[C/G]CGTGGTGGCGGGTGC	55884
rs187833731	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049297	AAATGGTAAAATTTT[C/T]GTAACCATCCTCTCA	55884
rs188041386	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118050061	AAAAATTAGCTAGGG[A/G]TGGTGGCGCATGCCT	55884
rs188165086	snp	C/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118056680	CCGAGGCAGGCAGGT[C/G]ACTTGGGGCCAGGAG	55884
rs188340160	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118037054	AGGCATGGTGGTGCA[C/T]GCCTGTAAGCCCAGC	55884
rs188457734	snp	A/G	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118041004	CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA	55884
rs188549952	snp	C/T	0.0123036	0.0774623	intron-variant	WSB2	GRCh38.p7	12:118045524	CCAATATGGTGAAAC[C/T]CCATCTCTACTAAAA	55884
rs188746056	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058649	GGCACCATTCACTTT[C/T]CTTTAACCATTTGAT	55884
rs188875155	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118057952	AATTAAATTTTTAGT[A/G]GAGATGGGGGTCTGG	55884
rs189061222	snp	A/G	0.0283406	0.115616	intron-variant	WSB2	GRCh38.p7	12:118045282	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG	55884
rs189091218	snp	C/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118050216	AACTACGCAACCAAG[C/G]CTGGCTGAATGAATA	55884
rs189114662	snp	C/T	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118042429	TTATCCAGCCCAAAA[C/T]ATCCATAGTGCCGAT	55884
rs189171282	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118032803	CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	55884
rs189180289	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040723	ACATCTTAGACTGTG[G/T]GATTACAGGTTCCAC	55884
rs189185249	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033716	GCACTTGGCCAACAT[C/G]GAAGCAACTCTGACC	55884
rs189191718	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051697	ATGTGCCAGGCACAG[C/T]GGCTCATGGGAGAAA	55884
rs189431530	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050769	ACCTGAAAAGATGCT[C/T]GGCCAGGTGTGGTGG	55884
rs189728089	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118055807	TTTAGTAGAGACAGG[C/T]TTTTGCTATCTTGGC	55884
rs189747831	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063285	CTACTAAAAATACAA[A/C]AATTAGCTGGGTGTG	55884
rs189772207	snp	A/G	0.000280082	0.0118306	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043203	CAGGCAAGAGACATC[A/G]GGCACTTGGGGGTGG	55884
rs189974491	snp	A/C/G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039416	GTTTAATGAAAAATG[A/C/G/T]GAGATGCAGGGAAAA	55884
rs189989971	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037532	AATTAGCCAGGCGTG[A/G]TGTAGCACGCCTATA	55884
rs190000567	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057897	CTGTGTATCGGGCTA[C/T]GGGGGCGTACCACCA	55884
rs190010695	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118040526	AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCC	55884
rs190139240	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118039930	TACATATTTTTAGTA[A/G]AGCCGGAGTTTCACC	55884
rs190155267	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118056924	AAAAAATAAATAAAG[C/T]CCCTTAAACTCTGAT	55884
rs190255285	snp	A/G	0.00517822	0.0506191	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032402	GTACCTGGAACTTCA[A/G]GATAACCATGAAATG	55884
rs190258828	snp	C/G	0.00438332	0.0466095	intron-variant	WSB2	GRCh38.p7	12:118059580	GCAGCTCTCAACAAC[C/G]CTGCCCACACCCTCA	55884
rs190284903	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062230	GGCCAGGGCAGGAGT[A/C]ATCATGGAGGCTTTT	55884
rs190409681	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048418	CATGGTGAAAACTTG[C/T]CTCTTCTAAAAATAC	55884
rs190648757	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044453	TCATCTTGCCAACAC[C/T]GTTTGTTTGGTACAT	55884
rs190691817	snp	A/G	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118035512	CAGAAGGCTCCAGGT[A/G]TCCTGTGGATGAAGG	55884
rs190769739	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041912	GGCGCCCACCACCAC[A/G]CCCAGCTCATTTTTG	55884
rs190809868	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118047671	TGAGCTATGATCATG[A/C]CACTGTACTCCAGCC	55884
rs190979761	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118053461	AAACGGAAATAAGTC[A/G]CACCTTGTTTATTTC	55884
rs191079279	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057197	AAAACAGAGCTGGGG[C/G]TGGGGTATCTAGCTT	55884
rs191218680	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118045124	GCTCATGCTTGTAAT[C/T]CCAGCACTTTGGGAG	55884
rs191306993	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118048886	GAGCTTTCCCCAACC[A/G]ACACATGCTCCACAC	55884
rs191393274	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059159	AAGTCAGAATTCAGA[G/T]GGGCTGTAAGTAAAA	55884
rs191464363	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118041457	TAAGCCACCCAGTCT[C/T]TGGCATTGACTAAGA	55884
rs191482729	snp	A/C	0.00676609	0.0577691	intron-variant	WSB2	GRCh38.p7	12:118041058	CGTCTCAAGAAAAAA[A/C]AAACAAACCAAAAAA	55884
rs191484873	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058869	GCCTGGTTAATTTTG[C/T]ATTTTTAGTAGAGAC	55884
rs191746632	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056247	ACATTGCCCTTCTCT[C/T]TACCCTCTGCCAATG	55884
rs191754911	snp	A/T	0.00104174	0.0227988	intron-variant	WSB2	GRCh38.p7	12:118052307	CAGTACGAGAATACT[A/T]ACAACTGCTCCTCCA	55884
rs191764273	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118058465	ATGATCCTCCCATCT[C/T]AGCCTCCCCAGTAGC	55884
rs191868771	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063782	GCACTTATTGCATCA[C/T]AATACATTTTGCCTA	55884
rs191898027	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034687	GTTACCTGTAAAGTG[A/G]TCTTTTAGCCCTAAA	55884
rs192181011	snp	A/G	0.0150606	0.0854603	intron-variant	WSB2	GRCh38.p7	12:118043839	GAGTTGATGTAGGCC[A/G]GGCGTGGTGGCTCAT	55884
rs192360657	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118036074	AGGCCTGGTGGCGCA[C/T]GCTTGTAGTCCTAGC	55884
rs192368604	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054602	TTGAACCCGGGAGGC[A/G]GAAGGCAGAGGTTGC	55884
rs192513059	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118049454	TTACCCAGGCTGGAG[G/T]GCAGTGGCGCGATCT	55884
rs192560389	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032444	CAATCCATTCCCAGC[A/T]CTTCTGCTGTACTAC	55884
rs192572993	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032312	ACTCACCCCCTTAAG[A/G]ACAGCGGCAAAGTAT	55884
rs192576103	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118050172	CCCGGGCGACAGAGC[A/G]AGACTCCATCTCAAA	55884
rs192829866	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050509	GGCTGGGCATGGTGG[C/T]GCGCCTGTAGTATCA	55884
rs192876816	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040785	AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	55884
rs192990146	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054922	GGTGGCTCACGCCTA[C/T]AATCCTAGCACTTTG	55884
rs193203845	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037084	CTATTTGGGAGGTTG[A/G]GGCAGAAGAATCACT	55884
rs193214381	snp	C/T	0.0107246	0.0724382	intron-variant	WSB2	GRCh38.p7	12:118045236	GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	55884
rs199554251	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046484	AAAAAAAAAAAAAAA[C/T]AAAGAAAAAATTTGT	55884
rs199674891	in-del	-/A	0.0685596	0.171987	intron-variant	WSB2	GRCh38.p7	12:118048682	TAAATAATAAATATG[-/A]AAAAAAATGGTTAAT	55884
rs199720753	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118050857	AGGAGTTTGAGACCA[G/T]CCTGGCCAACATAGT	55884
rs199743615	snp	C/T	8.23757e-05	0.00641725	missense	WSB2	GRCh38.p7	12:118034342	CTGTCCAGAACTGGA[C/T]GTGGCCATCTCTTGT	55884
rs199804263	snp	C/T	5.15743e-05	0.00507784	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043329	GCTGCCCCGCCCTTT[C/T]GTCTCATTTTTGCTA	55884
rs199833026	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118040231	AGGGTGCTGGGAGTA[C/T]TGAATAAATTAAGGC	55884
rs199856963	in-del	-/AAT			intron-variant	WSB2	GRCh38.p7	12:118054682	AACTCTGTCTCAAAA[-/AAT]AATAATAATAATAAT	55884
rs200081022	snp	C/T	0.00050528	0.0158866	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043311	CAGCGTCTTCTCTTT[C/T]GGGCTGCCCCGCCCT	55884
rs200105998	snp	G/T			missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042893	CCGTGACGCGGAGAC[G/T]AAAATCAAACTGCCA	55884
rs200118115	snp	A/C/T	1.69378e-05	0.00291009	intron-variant	WSB2	GRCh38.p7	12:118036299	AGGTTCCTCATCAGT[A/C/T]CCCCCACAAAAAAGT	55884
rs200187600	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034370	TGTCCTAAAATGAAA[C/T]AGAAACCGATGCTAA	55884
rs200282967	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118054687	TGTCTCAAAAAATAA[A/T]AATAATAATAATAAT	55884
rs200311345	snp	C/T	1.66313e-05	0.00288364	intron-variant	WSB2	GRCh38.p7	12:118036335	CAGGGATTCAGTCCT[C/T]ACTGGAGTGACCTCA	55884
rs200548315	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050841	TGGATCACCTGAGGT[C/T]AGGAGTTTGAGACCA	55884
rs200618171	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034173	TTTACCCTGCTACAA[A/G]GAAGCACAAGATGTG	55884
rs200647044	snp	C/T	8.24069e-05	0.00641846	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052395	CATCTGGGGAGAAGG[C/T]GACGCTCCAGGTTTC	55884
rs200763211	snp	C/T	0.000514766	0.0160349	intron-variant	WSB2	GRCh38.p7	12:118035143	GACCCAGGGCCAGAC[C/T]AAGAGGGCCTTGCTG	55884
rs200790728	snp	C/G	8.41319e-05	0.00648528	intron-variant	WSB2	GRCh38.p7	12:118038396	CTGTTTACCTGGCAG[C/G]AAAAAGAAGCAAACA	55884
rs200814476	in-del	-/CT			intron-variant	WSB2	GRCh38.p7	12:118050632	CAACAGAGCAAGACC[-/CT]CTCTCTCTCTCAAAA	55884
rs200858825	snp	C/G	6.68784e-05	0.00578228	intron-variant	WSB2	GRCh38.p7	12:118052513	GCTTCAAACACACAC[C/G]CCCTTGCTCCCTGAC	55884
rs200962451	snp	G/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118057777	ATATATATATTTGGG[G/T]TTTTTTTTTTTTTGA	55884
rs201003855	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118050880	AACATAGTGAAATCT[C/G]GTCTCTACTAAAAAT	55884
rs201007359	snp	G/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118037664	CAACAGCGAAACTCT[G/T]TCTAAAAAAAAAAAA	55884
rs201312471	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118037060	GGTGGTGCACGCCTG[-/T]AAGCCCAGCTATTTG	55884
rs201689442	snp	A/G	1.65718e-05	0.00287848	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038367	CACTGCAGGTGGCCC[A/G]ATAACACTTGAATCT	55884
rs201738429	snp	A/C	0.000451441	0.0150172	intron-variant	WSB2	GRCh38.p7	12:118052289	ATGCGCCGGATGGGG[A/C]CCCAGTACGAGAATA	55884
rs201745633	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118039744	AATATTTCTTTTTTA[-/T]TTTTTTTTTATTTTT	55884
rs201745643	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056100	CCCCGCACCATCGGT[C/T]CTCCTTGCCTCCAGA	55884
rs201779847	in-del	-/T	0.00835141	0.0640778	intron-variant	WSB2	GRCh38.p7	12:118059314	CCTAGTTCTTTTTTC[-/T]TTTTTTTTAATGTGG	55884
rs201822111	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118051192	TAAAAAAAGACAGAC[A/T]ATAACAACGGCTGGA	55884
rs201888386	snp	A/C	0.00217466	0.0329029	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034164	ACAGGACGATTTACC[A/C]TGCTACAAAGAAGCA	55884
rs201907723	snp	G/T	1.64931e-05	0.00287163	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043243	CAGAGCTTCCTGCTG[G/T]GTGGGGAAGGCCACG	55884
rs202062993	snp	A/G	1.64838e-05	0.00287083	synonymous-codon	WSB2	GRCh38.p7	12:118035081	CAGTTCCAGGGCCCA[A/G]ATCCTGAGGAGTCTG	55884
rs202087094	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118059224	AAAAATCTAAAACAT[A/T]ACATTACAATTTATT	55884
rs202169586	snp	A/G	0.000626835	0.0176925	synonymous-codon	WSB2	GRCh38.p7	12:118036361	CCTCAGCCTTTCGCC[A/G]GTGTAGGGGTCCCAC	55884
rs367626923	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118057791	GTTTTTTTTTTTTTT[G/T]AGACCCAGGCTGGGG	55884
rs367751201	snp	C/G	1.64836e-05	0.0028708	intron-variant	WSB2	GRCh38.p7	12:118043118	AGAACCTTGTGCCAG[C/G]CAGGAATGACCTACC	55884
rs367755685	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	WSB2	GRCh38.p7	12:118034301	TTTCCGGCATAAGTG[C/T]TTCAGTGAGGACAGG	55884
rs367765070	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118036648	TTTTCTACAGCTCTT[C/T]CAGAACGTGTGGTGT	55884
rs367876002	snp	C/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118054573	TACTCAGAGGGCTGA[C/G]GCAGGAGAATCGCTT	55884
rs367940419	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053531	CTCGTCATCAGTGTC[C/T]AAGCACCTTGTTCCA	55884
rs368149295	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039390	GAGAGATTTTCCATG[A/G]GGTACCTACAGTTTA	55884
rs368150064	snp	C/T	0.000115486	0.007598	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034155	CTCCCTTTGACAGGA[C/T]GATTTACCCTGCTAC	55884
rs368155185	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118058070	GTTCTAATTAAACAA[C/T]GGGATGTGTTTGGAC	55884
rs368295246	in-del	-/AG			intron-variant	WSB2	GRCh38.p7	12:118039064	TCATTCCCAATTTTA[-/AG]AGAGTGTTTATCTTC	55884
rs368393260	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032546	GATCGTGGCTCGCTA[C/T]AGCCTCCATGTCCCA	55884
rs368398081	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118052874	AGAAGAACCTGCTGC[C/T]GTCAAAGAAGGAATA	55884
rs368400372	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118035931	ATGAACCAGGCCAGG[C/T]GCAGTGGCTCATGCC	55884
rs368402513	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055780	CCACCACACCCAGCT[A/G]ATTTTTGTATTTTTA	55884
rs368433007	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044953	ACATCTTTATGTATT[A/C]ATTGGTGCGAAAATA	55884
rs368496001	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050159	CATCGCACTCCAGCC[C/T]GGGCGACAGAGCGAG	55884
rs368521850	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062569	TTCCTAACGCAACCT[A/G]TGTTTTCTACGGTAA	55884
rs368540564	snp	A/G	0.000329592	0.0128331	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043223	CTTGGGGGTGGTGGC[A/G]TGCCCAGAGCTTCCT	55884
rs368558947	snp	C/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064034	TAAATAGATCTCATG[C/G]TCTCTAAGTTAACAA	55884
rs368652324	in-del	-/AATAAT			intron-variant	WSB2	GRCh38.p7	12:118054682	AACTCTGTCTCAAAA[-/AATAAT]AATAATAATAATAAT	55884
rs368693869	in-del	-/CT/CTCT/CTCTCT/CTCTCTCT	0.114953	0.215741	intron-variant	WSB2	GRCh38.p7	12:118034574	TGTGATACCAAAGCG[-/CT/CTCT/CTCTCT/CTCTCTCT]CTCTCTCTGTCTCTC	55884
rs368742788	snp	A/G	3.38301e-05	0.00411265	intron-variant	WSB2	GRCh38.p7	12:118036296	GGCAGGTTCCTCATC[A/G]GTCCCCCCACAAAAA	55884
rs368811902	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118050955	TACTTGGGAGGCTGA[C/G]GCAGGAGAATTGCTT	55884
rs368886729	snp	C/G/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118041128	AGGATGCATGTGCAC[C/G/T]GCCTTAGTTTGTCTG	55884
rs368891609	snp	A/G	0.000153988	0.00877328	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052406	AAGGCGACGCTCCAG[A/G]TTTCACAGCTGGACT	55884
rs369032562	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118052558	AAAGCCACTGTCTCC[C/T]TGTGGCAAAGAGCCA	55884
rs369151920	snp	A/C			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063492	AGAAGAATATTGTTA[A/C]CAATTTTTAAAAAGC	55884
rs369215956	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056757	AATACAAAAATTAGC[C/T]GGGCATAGTGGCGGG	55884
rs369228148	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062748	CCGGTTTTTTTTTTT[C/T]TTTTCTTTGAACCTG	55884
rs369228308	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118048430	TTGTCTCTTCTAAAA[A/G]TACAAAAAAATTAGC	55884
rs369386906	snp	A/G	4.96907e-05	0.00498426	intron-variant	WSB2	GRCh38.p7	12:118034961	CAGAAAGCACCACCC[A/G]TCTGTTCAGCTAACA	55884
rs369529630	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046916	AGCTGGGACTACAGG[C/T]GCATGCCACCATACC	55884
rs369543349	snp	A/G	3.38461e-05	0.00411362	intron-variant	WSB2	GRCh38.p7	12:118052278	AGTGTTTGGAAATGC[A/G]CCGGATGGGGCCCCA	55884
rs369585350	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118059499	GCCCATTGTATTTCC[C/T]TTACAATGGGCTTTA	55884
rs369755766	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058421	AGCACCATCACGGCT[C/T]ACTGCAACCTCGACC	55884
rs369806233	snp	A/G	3.30595e-05	0.00406554	intron-variant	WSB2	GRCh38.p7	12:118034378	AATGAAACAGAAACC[A/G]ATGCTAAGACAGAGC	55884
rs369830819	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118035493	GGGAAAAAAAAGGGT[A/G]TCTCAGAAGGCTCCA	55884
rs369847771	snp	A/G	0.000153988	0.00877328	synonymous-codon	WSB2	GRCh38.p7	12:118036442	GGAGAAGTCACAAGA[A/G]ACAACACTGCTTTGA	55884
rs369977350	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045419	TTAGAAGGGAGGGGC[C/T]GGGCACGGTGGCTCA	55884
rs369983698	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063184	GCTCATGCCTGTAAT[A/C]CCAGCACTTTGGGAG	55884
rs370046925	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118035902	CTTAATTGACAAGGC[A/T]TCACTAAGAAGCAAT	55884
rs370058374	snp	A/C	1.67964e-05	0.00289792	intron-variant	WSB2	GRCh38.p7	12:118042792	GTAAAGTGGAGAAAG[A/C]AAATACAGTATTTTT	55884
rs370201070	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118056035	GCAGCATCATCTCCC[A/G]CCTGGCCCAGTAGGC	55884
rs370278171	snp	A/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118060822	TCGCCGGCGGGAGTC[A/T]GGGTGGCGGCCACTG	55884
rs370303911	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118038837	AGGGATGTGCCACTG[C/T]GCCCAGCTCATTTTT	55884
rs370376135	snp	A/G	4.95864e-05	0.00497903	intron-variant	WSB2	GRCh38.p7	12:118043017	CCAGAGAGGGGGCAC[A/G]AGGTGTGCCTGCCAC	55884
rs370416239	snp	A/T	9.88517e-05	0.00702966	missense	WSB2	GRCh38.p7	12:118035041	AAAGCCCATTGGTCA[A/T]AGGAGCAAATGCAAT	55884
rs370440793	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118053620	AGTAGGCACCAGATT[A/G]GAGCTTCTTCATTGA	55884
rs370472205	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118052721	TTGTGCCCATGAACC[C/T]AGTGAATGGAGGCCT	55884
rs370512271	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118037655	CTTGGGCAACAACAG[C/T]GAAACTCTGTCTAAA	55884
rs370700415	snp	A/G	3.29685e-05	0.00405995	intron-variant	WSB2	GRCh38.p7	12:118035209	AAGAGAGTTCTCTTC[A/G]TTACCTGTCATCTGC	55884
rs370734147	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118056527	TATCCCCAGAGCTGG[C/T]AGAGTTCCTGGTGGA	55884
rs370986997	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118032829	ATTACAGGCATGTGC[C/T]GTCACACCCAGCCCT	55884
rs371103196	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035390	ACCCTCCATCATCAC[C/T]CTAGGCAGGAAGCCA	55884
rs371223023	snp	C/G	3.32071e-05	0.00407461	intron-variant	WSB2	GRCh38.p7	12:118042826	GTTGCCGAGTAGTTC[C/G]TTCACTTCCCATACC	55884
rs371247871	snp	A/G	4.94972e-05	0.00497455	intron-variant	WSB2	GRCh38.p7	12:118035193	GTTCTGAGGCCATGT[A/G]AAGAGAGTTCTCTTC	55884
rs371289132	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046168	AGCCTAAACTATTTA[C/T]AGAAAAAGTTGGCCA	55884
rs371352502	snp	A/G	0.0622301	0.165053	intron-variant	WSB2	GRCh38.p7	12:118060908	CGGACCTCCCAGGCC[A/G]GACGCCCCCGCCGCG	55884
rs371401263	snp	A/G	0.00874735	0.0655527	intron-variant	WSB2	GRCh38.p7	12:118052918	GGCTCCCTCTCACTC[A/G]CCTGCATCCTCCCCA	55884
rs371563655	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118041622	CTCCTTCCAATCCCT[C/G]CAGCCCCTGATCCTC	55884
rs371661725	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118042740	AATCACAGAAAAAAA[-/A]CATCAAGAAACACTG	55884
rs371694946	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045714	AGACACTGTCTCAAA[A/G]AAAAAAAAAAAAAAA	55884
rs371785935	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033673	AGGAAAACTGTCCTG[C/T]AGGTCAGAAGGGAGC	55884
rs371864468	snp	C/T	4.18121e-05	0.00457212	intron-variant	WSB2	GRCh38.p7	12:118038237	CACACCAGGCCACCA[C/T]TTCAGACCTCCATGT	55884
rs371896890	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051087	AAAGAAAGAAAAGAC[A/G]CTTGACATCCATAGC	55884
rs371908533	snp	C/G	0.000148386	0.00861227	missense	WSB2	GRCh38.p7	12:118035309	GTCATCCATGGCGGG[C/G]TCAACCTGGGTGTGG	55884
rs371935763	snp	C/T	0.000104205	0.00721744	intron-variant	WSB2	GRCh38.p7	12:118038428	TGAGCCAGTCCTCAA[C/T]AAAGCAGGAAGACTG	55884
rs371958499	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118058281	TCATTCAGGGATTGG[A/T]CCTCATGTCACCTTC	55884
rs372026056	snp	A/C			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062655	TTTTTACCCAGGCCC[A/C]TGTTTTATGAGCCCT	55884
rs372073086	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118054789	GTGTGTGTTCCTGAA[C/G]TTTCTGTCTTTAAAT	55884
rs372130606	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118048246	TAGCCTGTTTTTTTT[-/T]CAATAAGCCTCATAC	55884
rs372181768	snp	C/G	1.65321e-05	0.00287502	missense	WSB2	GRCh38.p7	12:118036352	CTGGAGTGACCTCAG[C/G]CTTTCGCCGGTGTAG	55884
rs372304637	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050280	AAACATACAGATGCT[A/G]GGCCATCTGAATGGG	55884
rs372440105	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039636	AAGGAAAGAGCCAAG[C/T]AAGAAAGAAGAAAAA	55884
rs372595865	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118041176	AAATGTGCCCCCCAC[A/T]CATAAAGCCCTAATC	55884
rs372880021	snp	C/T	0.0142736	0.0832652	intron-variant	WSB2	GRCh38.p7	12:118036728	GGCATGCTCAAGGAG[C/T]TCACTATAAGAGAGA	55884
rs372927594	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046639	CTCTGGCCCTGGCAC[C/T]GGCCCCTGAGTTTGT	55884
rs372929280	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118042229	AAGTCTTTCTTTCTA[A/G]CAGGAAGCACCCAAC	55884
rs373199546	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118052515	TTCAAACACACACCC[C/T]CTTGCTCCCTGACCA	55884
rs373392059	snp	A/G	0.000153988	0.00877328	intron-variant	WSB2	GRCh38.p7	12:118034978	CTGTTCAGCTAACAA[A/G]TACATACCCTGTGGC	55884
rs373415947	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063519	AAGCTAGTAAAAAAA[A/T]TTTTTTTTGGCAAGT	55884
rs373461745	snp	C/G/T	4.96909e-05	0.00498432	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038366	CCACTGCAGGTGGCC[C/G/T]GATAACACTTGAATC	55884
rs373493543	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051763	TGAATCACTTGAGGT[C/T]AGGAGTTTGAGACCA	55884
rs373702219	snp	C/T	0.00953873	0.0683987	intron-variant	WSB2	GRCh38.p7	12:118055778	CACCACCACACCCAG[C/T]TAATTTTTGTATTTT	55884
rs373782508	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032456	AGCTCTTCTGCTGTA[C/T]TACTTGTTTTATGTG	55884
rs373828240	snp	C/T	3.29679e-05	0.00405991	intron-variant	WSB2	GRCh38.p7	12:118043110	AGCCTCCCAGAACCT[C/T]GTGCCAGCCAGGAAT	55884
rs374117858	snp	C/G/T			intron-variant	WSB2	GRCh38.p7	12:118037404	AGGCGCGGTGGCTCA[C/G/T]GCCTGCAATCCCAGC	55884
rs374123497	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118058240	TTCCACCGGCCTCAA[A/C]AGCTTTCCTCAGTTG	55884
rs374137042	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118035439	AGGGCTCAAGATGCA[C/T]TGTGTGCCCCTCGTG	55884
rs374142056	snp	C/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118052730	TGAACCCAGTGAATG[C/G]AGGCCTCATTTTCCT	55884
rs374162595	snp	A/G	0.00636936	0.0560724	intron-variant	WSB2	GRCh38.p7	12:118048024	CTCTAATTCCTGGGT[A/G]CAGGTGATCCTCCCA	55884
rs374194363	snp	A/G			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062559	ATTTCTTTGCTTCCT[A/G]ACGCAACCTATGTTT	55884
rs374246644	snp	G/T	1.65252e-05	0.00287443	intron-variant	WSB2	GRCh38.p7	12:118043007	ACTGAGTCAGCCAGA[G/T]AGGGGGCACGAGGTG	55884
rs374294553	snp	A/G			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061631	AAAAACCAAGCAGGG[A/G]AAGCGGCGATCCGGG	55884
rs374370160	in-del	-/AG	0.00716266	0.059414	intron-variant	WSB2	GRCh38.p7	12:118042478	TCAAATATTTTTAAC[-/AG]GGGCAATTCACCCCA	55884
rs374451281	snp	C/T	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118049960	TTTATCTAACGACTC[C/T]CAGTCCCTAACTCAG	55884
rs374531933	snp	C/T	0.000117221	0.00765484	intron-variant	WSB2	GRCh38.p7	12:118042806	GCAAATACAGTATTT[C/T]TGGAGTTGCCGAGTA	55884
rs374539278	snp	C/G	1.64789e-05	0.0028704	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043213	ACATCGGGCACTTGG[C/G]GGTGGTGGCGTGCCC	55884
rs374676927	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049319	ATCCTCTCATCCCTG[A/G]ATTTCAAACTGTTTC	55884
rs374683699	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118057306	TTGAGACAGAGTCTC[A/T]CTCTGCTGCCCAGGC	55884
rs374731610	snp	A/C/T	4.9842e-05	0.00499189	intron-variant	WSB2	GRCh38.p7	12:118035346	AGGAAAGAAACAGGA[A/C/T]GGCAGGCCTGGAGTG	55884
rs374860011	snp	A/C	0.000153988	0.00877328	missense	WSB2	GRCh38.p7	12:118035241	ACCGTGGCAAGGTAC[A/C]AGCCTTCTGGAGAGA	55884
rs374964769	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046231	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTTGA	55884
rs374989488	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060836	CAGGGTGGCGGCCAC[C/T]GACAACGAAAGTGAA	55884
rs375019408	snp	A/C/G	0.00953873	0.0683987	intron-variant	WSB2	GRCh38.p7	12:118044793	AAGCTTACTGTTTGC[A/C/G]GTACACAGCACAAAG	55884
rs375021192	in-del	-/TTT	0.029116	0.117091	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063520	AGCTAGTAAAAAAAA[-/TTT]TTTTTGGCAAGTTCG	55884
rs375025061	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036240	TATCCAGCTTGTCCC[C/T]TCCCATGTCCCAGAT	55884
rs375121581	snp	A/G	1.66054e-05	0.00288139	intron-variant	WSB2	GRCh38.p7	12:118034944	CTCCATGGTATACTC[A/G]GCAGAAAGCACCACC	55884
rs375180176	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118059811	AAAAGAAAGCCCTTA[C/T]CTAGATGGGAAGGAG	55884
rs375339533	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033387	ATCGAGAAAAACACA[A/G]TTGTACCTTAACATC	55884
rs375350697	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045329	GAGATCGCACCACTG[C/T]ACTCCAGCCTGGGCA	55884
rs375373131	snp	C/T	0.0240643	0.107019	intron-variant	WSB2	GRCh38.p7	12:118056793	GTAGTCGCAGCTACT[C/T]GGGAGGCTGAGGCAG	55884
rs375427460	in-del	-/TC			intron-variant	WSB2	GRCh38.p7	12:118050643	GACCCTCTCTCTCTC[-/TC]AAAAAAAATAAATGA	55884
rs375468145	snp	A/C			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033285	CTCGTACATAAGAGT[A/C]TCAGCTAAAGTCATG	55884
rs375572140	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063404	ATCTTGCCATTGCAC[A/T]CCAGCCTGGGTGATG	55884
rs375700459	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056326	TGGAATGCCTCTCCT[C/T]GGCTGGCATCTACTC	55884
rs375723736	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118036047	TCTCTAATAAAAATA[C/T]AAAAATTAGCCAGGC	55884
rs375879070	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063375	CCAGGAGGTGGAGGT[C/T]GCAGTGAGCTGAGAT	55884
rs375957763	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050881	ACATAGTGAAATCTC[A/G]TCTCTACTAAAAATA	55884
rs376167607	snp	G/T	4.11336e-05	0.00453488	intron-variant	WSB2	GRCh38.p7	12:118038250	CACTTCAGACCTCCA[G/T]GTCTCAGTGAATTAA	55884
rs376185861	snp	A/G	1.80426e-05	0.00300349	intron-variant	WSB2	GRCh38.p7	12:118043386	AGGGATGCTGGGAGA[A/G]GCAGAGATTTCTTAA	55884
rs376192132	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118048527	GGAGGCAGAGGTTAA[A/G]GTGAGCCGAGATGCG	55884
rs376406600	snp	C/T	1.6476e-05	0.00287014	missense	WSB2	GRCh38.p7	12:118035039	GCAAAGCCCATTGGT[C/T]ATAGGAGCAAATGCA	55884
rs376566617	in-del	-/T	0.398534	0.201091	intron-variant	WSB2	GRCh38.p7	12:118055912	AAACCACCACGTCTG[-/T]TTTTTTTTTTTTAAA	55884
rs376577368	in-del	-/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062747	CCGGTTTTTTTTTTT[-/T]CTTTTCTTTGAACCT	55884
rs376595091	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118036812	TCTGAGTCTGCTTCT[G/T]AGTCCTGTTTGCCAA	55884
rs376677143	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118035823	TCATAATGCTGATTC[C/T]GAAGAAGTACACACA	55884
rs376688488	snp	A/G	0.00874735	0.0655527	intron-variant	WSB2	GRCh38.p7	12:118054527	AATACAAAATAAGCC[A/G]GGCTTGGTGGCGCAT	55884
rs376748690	snp	A/G	0.00795532	0.062565	intron-variant	WSB2	GRCh38.p7	12:118042631	AAATAGACACACAGT[A/G]TATGTTCGGTATTAA	55884
rs376760156	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118042046	CAGGCGTGAGCCACT[G/T]TGCCTGGCCTCTTAT	55884
rs376897864	snp	C/T	1.66902e-05	0.00288874	intron-variant	WSB2	GRCh38.p7	12:118042816	TATTTTTGGAGTTGC[C/T]GAGTAGTTCCTTCAC	55884
rs376973021	snp	C/G/T	4.96638e-05	0.00498296	intron-variant	WSB2	GRCh38.p7	12:118052305	CCCAGTACGAGAATA[C/G/T]TTACAACTGCTCCTC	55884
rs377017238	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118035452	CATTGTGTGCCCCTC[A/G]TGGAAAAGCTTGGGA	55884
rs377167512	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041414	ACTCCCCAACCTTCA[A/G]AACTGTGAGAAATAA	55884
rs377247037	snp	C/T	4.96126e-05	0.00498035	intron-variant	WSB2	GRCh38.p7	12:118043016	GCCAGAGAGGGGGCA[C/T]GAGGTGTGCCTGCCA	55884
rs377282783	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118046876	TCCAGGGCTCGAGCA[A/G]TCCTTCCATCTCAGC	55884
rs377344969	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118060197	GCGTGCATGCGTCTT[A/G]GGGTTTTTTTCCCCT	55884
rs377469213	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049350	CAATTTTCTTAACAT[A/G]CAACTAATTTCATGA	55884
rs377603158	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037561	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	55884
rs377605496	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118058413	AATGCAGTAGCACCA[C/T]CACGGCTCACTGCAA	55884
rs377656379	snp	A/G	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032531	GGAATACCGTGACAC[A/G]ATCGTGGCTCGCTAC	55884
rs377707762	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118037213	CAGAAGTGAAATCTG[C/T]GGCCACCCCACAAAG	55884
rs377725473	snp	C/T	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118047813	ACAAAGTAAAAATTA[C/T]CTATAATCCTAACAC	55884
rs377757315	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118060596	TCAGTGGCTTGTCCA[C/T]TGTCACGATCACACA	55884
rs386766822	in-del	ATC/TG			intron-variant	WSB2	GRCh38.p7	12:118037950	AGAGGGATTCAAATT[ATC/TG]ATGGTTCAAAGGAAA	55884
rs386766823	multinucleotide-polymorphism	AA/TC			intron-variant	WSB2	GRCh38.p7	12:118050643	GACCCTCTCTCTCTC[AA/TC]AAAAAAAATAAATGA	55884
rs397773927	in-del	-/T	0	0	intron-variant	WSB2	GRCh38.p7	12:118057790	GTTTTTTTTTTTTTT[-/T]GAGACCCAGGCTGGG	55884
rs397850089	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118058713	TCTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC	55884
rs397943553	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118059213	TAGCACAAAAAAAAA[-/A]TCTAAAACATTACAT	55884
rs527265053	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060628	CTTGTGAGGGACAGA[C/G]GTGACTCCCATCCAG	55884
rs527298809	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059393	TGGTCGGGGCTGGCC[G/T]AGAGGGTGCCTGGCA	55884
rs527344002	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118043942	GCCAACATGGTGAAA[C/T]CCCATCTCTACTAAA	55884
rs527392121	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118046661	TGAGTTTGTTGTCAC[A/G]AGAAGCAGCACTTAA	55884
rs527439308	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033633	TTTAGTTAAGCTAAA[C/T]TAATACCTCATACCA	55884
rs527572324	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118040156	CCAGCCCATGCAACA[C/T]AGTGAGACTCTGTCT	55884
rs527643176	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035627	TTTTAGGCTAAGATA[C/T]ATGATAATTATAGGA	55884
rs527817477	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041329	ATGAGGATGCAGAGA[C/G]AAGGTGGCTGTTTAC	55884
rs527844449	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040746	GGTTCCACAGTACTG[A/G]GCAGAAACCACCTAG	55884
rs527845385	in-del	-/T			utr-variant-3-prime, intron-variant, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118032864	GTTTTAAAAGGGGAC[-/T]TTTTTTTTTCTTAAT	55884
rs527849127	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047769	TAAATAAAAATAGTA[C/G]CGAAACATGGGAGAA	55884
rs527884878	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054388	AGAGCGAGACTCTGT[C/T]TCAAAAAAAAATTGG	55884
rs527981167	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046892	TCCTTCCATCTCAGC[C/T]TCCTGAGTAGCTGGG	55884
rs528020996	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053632	ATTGGAGCTTCTTCA[C/T]TGACTGACCCACAGT	55884
rs528168507	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049503	GCCTCCCAGGTTCAC[A/G]CGATTCTCCTACCTC	55884
rs528258819	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118055455	GGATGGCCTGGGGTA[A/G]TGGCTCATGCCTGTA	55884
rs528302911	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	WSB2	GRCh38.p7	12:118062393	TGCTTTGGGCCCAAG[C/T]TCTTCCCGCGGTTCT	55884
rs528380711	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058480	CAGCCTCCCCAGTAG[C/T]TGGGACTACAGGCAC	55884
rs528606624	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064090	AGCACAGTGTAACAA[C/T]TTGGACTTTGCCACA	55884
rs528741694	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036931	TCATGCCTGTAATCT[A/C]AGCACTTTGGGTGGC	55884
rs528801553	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043109	GAGCCTCCCAGAACC[A/T]TGTGCCAGCCAGGAA	55884
rs529170480	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043967	ACTAAAAAAAAAAAA[C/T]AATTCGCCGGGCGTA	55884
rs529206832	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118050921	TCTAGGCGTGGTGGT[A/G]TGTGCCTGTAGTCCC	55884
rs529326460	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037161	CACTCCAGCTTGGGC[A/G]AAAGAGTAAGACTGT	55884
rs529384737	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046155	TTATGGCCCACAAAG[A/C]CTAAACTATTTATAG	55884
rs529444458	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052887	GCTGTCAAAGAAGGA[A/G]TATGTGAAACTCAAA	55884
rs529484784	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059187	AAAAATACACAACAC[A/G]TTTTGAACACTTAGC	55884
rs529636080	snp	A/C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058007	TCTCCTGAGCTCAAG[A/C/T]GATTCTCCTGCAGGC	55884
rs529651038	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053759	GTGATACTTACTAAT[A/G]TAAAAACTGGCTTCC	55884
rs529787729	snp	C/G	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118060763	GCCCCCTCTGTCCCG[C/G]TCGGGGGATCTCCTC	55884
rs529940443	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118036589	AGGGAAAGGTACCAC[C/T]ACCAAATCTGCAGGC	55884
rs529953998	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033732	GAAGCAACTCTGACC[A/G]CAGCAGGAGAGAACT	55884
rs529964908	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040512	ATACCTGTAATCCCA[G/T]CACTTTGGGAGGCCG	55884
rs530082458	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062552	ATTTTAAATTTCTTT[C/G]CTTCCTAACGCAACC	55884
rs530137837	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118057978	TCTGGCTATGTTGAC[C/G]AAGCTGGTTTTGATC	55884
rs530233009	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035701	AAGGAGACCAAGTTT[A/G]TGAGAACATGAAACT	55884
rs530305271	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118042561	CATACAAAGCATAGA[C/T]ATGCATTCAGCACAT	55884
rs530325485	snp	A/C	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118048499	GCTGAAGCAGGAGGA[A/C]CACTTGAATCCAGGA	55884
rs530591347	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118041496	TTCAGGCTCATTGCT[A/C]AAAGAGCAGGAGAAA	55884
rs530698832	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118049692	ACAGGCATCAGGTAC[C/T]GCGCCCAGCCCAGAA	55884
rs530759782	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063306	GCTGGGTGTGGTGGC[A/G]GGCACCTGTAAACCC	55884
rs530947075	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057565	CAGGCGTGAGTCACC[A/G]CGTCCAGCCTCTTCT	55884
rs531250386	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118037601	TGAACCCGGGAAGCG[C/G]AGGTTGCAGTAAGCC	55884
rs531274010	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118043439	CTATCAACTTTTCAT[C/T]CTGGGACACGTAAGA	55884
rs531283043	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033577	AAAGCCAGTAATAGT[A/G]TCTGGATCGGTCAGG	55884
rs531449193	snp	C/T	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032523	CCCAGGCTGGAATAC[C/T]GTGACACGATCGTGG	55884
rs531693197	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034429	GAGGATGAATACTCA[C/T]GTTTCTGTTTTGACT	55884
rs531814826	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060526	CCACCCTCCGAGGAA[G/T]GTACTAGGATTATCC	55884
rs531868123	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046756	TATAAAATCCTGATT[C/T]CTGTATTTGTTTTAT	55884
rs531906916	snp	A/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118046214	GCCTGTAATCCCAGC[A/T]CTTTGGGAGGCTGAG	55884
rs531942295	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052950	CATCAAGGCTAAAAA[C/T]GTTCAGCCCTTGCCC	55884
rs531945065	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048791	AAATAGGATTTAAAT[G/T]TATGGTTTGTTCAGA	55884
rs532070510	snp	C/T	0.00517822	0.0506191	intron-variant	WSB2	GRCh38.p7	12:118059277	TTTAGACATGTTGTA[C/T]TGAAAGAGTTTTTAA	55884
rs532120682	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051485	ATGAACTGTGAAAAC[A/G]TTATGTAAAATGAAA	55884
rs532217066	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118038449	AGGAAGACTGGAGAA[C/T]GGGAGAACTGGGGTG	55884
rs532276381	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118054526	AAATACAAAATAAGC[C/T]GGGCTTGGTGGCGCA	55884
rs532329272	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	WSB2	GRCh38.p7	12:118035021	ATGTGGAAAAAATGT[A/G]CAGCAAAGCCCATTG	55884
rs532351741	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063973	GAGAAAAACAAGAAA[A/T]AAGTCAGTTGCAATG	55884
rs532498726	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054004	TTTTTTTCTCAGTTA[C/T]ACATGATGATAATAC	55884
rs532558348	snp	C/T	1.65258e-05	0.00287448	missense	WSB2	GRCh38.p7	12:118036353	TGGAGTGACCTCAGC[C/T]TTTCGCCGGTGTAGG	55884
rs532656190	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042580	CATTCAGCACATAAG[C/T]AGATATACAATATAT	55884
rs532694041	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042035	TACTGGGATTACAGG[C/T]GTGAGCCACTGTGCC	55884
rs532916232	snp	A/G	1.66707e-05	0.00288705	missense	WSB2	GRCh38.p7	12:118038304	GACTTCTCTCCAGCT[A/G]CAGAGCACAGCATGC	55884
rs533116157	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118050818	ACACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	55884
rs533126914	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043437	GTCTATCAACTTTTC[A/G]TCCTGGGACACGTAA	55884
rs533156102	snp	A/G	0.00636936	0.0560724	intron-variant	WSB2	GRCh38.p7	12:118057314	GAGTCTCACTCTGCT[A/G]CCCAGGCTGGAGTGC	55884
rs533213749	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045607	ATCCCAGCTACTCAG[A/G]AGGCTGATGTGGGAG	55884
rs533308058	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051822	CTACTAATAATACAA[A/G]ACTTAGCCAGGCGTG	55884
rs533342585	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058232	ATTAGATATTCCACC[A/G]GCCTCAAAAGCTTTC	55884
rs533366265	snp	C/T	9.89169e-05	0.00703197	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052344	AGGGGATCAGTTTGA[C/T]GATGCAGTGTCCTTG	55884
rs533525416	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053062	TCTCATCTCACCCAG[A/C]TCTTTTGCTACAGTC	55884
rs533651875	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118047704	GGTGACAGAGCAAGA[A/C]CTTTTCTCTGCCCCC	55884
rs534257926	snp	A/G	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118046290	ACATGGTGATACCCC[A/G]TCTCTACTAAAAATA	55884
rs534345652	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033962	GGACTGAAAATTTAA[C/T]GTAAGGCTCTGTTGC	55884
rs534407042	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042137	TGTATATAGTTTGCT[C/T]GAGGCAGAATTTCAC	55884
rs534445136	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041658	GACCCTTTACCACTG[C/T]CTCCTTCCAATCCCT	55884
rs534530320	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039860	GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	55884
rs534667901	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045167	AGATCACGAGGTCAG[A/G]AGATCGAGACCACGG	55884
rs534682575	snp	A/G	1.67618e-05	0.00289493	intron-variant	WSB2	GRCh38.p7	12:118042799	GGAGAAAGCAAATAC[A/G]GTATTTTTGGAGTTG	55884
rs534824367	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047349	GCAGGGAGGTCGTAC[C/T]GTGGGAAAGAGCTGA	55884
rs534875824	snp	A/C	0.00835141	0.0640778	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063451	GAAAAAAAAAAAAAA[A/C]AAACAAAAAAGGCGG	55884
rs534912184	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062814	CTGTCCCTTTCTCGC[C/T]GCCCATGTTAACTTT	55884
rs534962423	snp	A/G	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118053971	AATCAATGACTTTTC[A/G]TAGTTAAATAGGTAG	55884
rs535143043	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118048360	TGGGAGGCCAAGGCA[A/G]GTAGATCCCTTGAGG	55884
rs535775196	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043445	ACTTTTCATCCTGGG[A/G]CACGTAAGACTTTTG	55884
rs535775973	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036658	CTCTTCCAGAACGTG[A/T]GGTGTAGGTTTAAAT	55884
rs535822309	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118051385	CAACCCAATGTCCAT[C/T]AACTGATAAATGTAC	55884
rs535846438	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047096	GTATTTGAATTAAGG[A/C]ATACACCTGTAGCTA	55884
rs535855190	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118057777	TATATATATTTGGGT[-/T]TTTTTTTTTTTTTGA	55884
rs535968488	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118042175	GATGCCCCATAGCCT[A/G]AGAGAATTATTCTAG	55884
rs535971592	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038777	CCTCTGCCTCCCAAG[C/T]TGAAGCGATTCTCCT	55884
rs536056943	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058987	AGACGTGAGCCACCC[C/T]GGCGCATTTGGTTGA	55884
rs536065958	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051918	GGCAGAGGTTGTAGT[A/G]AGCCAAGATTGCGCC	55884
rs536208650	snp	C/T	1.64844e-05	0.00287087	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042862	TATTCAGGTCCCAGA[C/T]GCGAAGAGTCTTATC	55884
rs536255305	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046366	TACTCGGGAGGCTGA[A/G]GCAGGAGAATCACTT	55884
rs536423001	snp	C/G	0.00398564	0.0444627	intron-variant	WSB2	GRCh38.p7	12:118060233	AAGAGACACACCTTT[C/G]CCACTGAGATTTTAT	55884
rs536580435	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040788	CGCAGTGGCTCACGC[A/C]TGTAATCCCAGCACT	55884
rs536625647	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054617	GGAAGGCAGAGGTTG[A/C]GGTGAGCTGAGATGG	55884
rs536701756	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061300	AAAAGATGGAAAATC[A/G]GGGAGGCGGTACGCT	55884
rs536783773	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036096	AGTCCTAGCTACTCG[A/G]GAGGCTCAGGCAGCA	55884
rs536808580	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042253	ACCCAACAGGGACTT[C/G]TAGATCAGTGGTTCT	55884
rs536898357	in-del	-/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118046465	GAGCAAGACTCCATC[-/T]CAAAAAAAAAAAAAA	55884
rs536970955	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118034016	TAAGACTGACTTTCA[A/C]ATGCCAGGGAGAGAA	55884
rs537023752	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037172	GGGCGAAAGAGTAAG[A/C]CTGTCTCAAATTTTT	55884
rs537052341	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043512	TACAGTGACACAATC[A/G]TGGCTCACTGCAGCC	55884
rs537087674	in-del	-/CT			intron-variant	WSB2	GRCh38.p7	12:118050631	CAACAGAGCAAGACC[-/CT]CTCTCTCTCTCTCAA	55884
rs537124305	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118056716	GACCAGCCTGGCCAA[C/T]GTGGTGAAACCCCGT	55884
rs537138145	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036566	GTGCTTAGGACTCAA[A/G]CGGAGGGAGGGAAAG	55884
rs537188346	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050529	CTGTAGTATCAGGTA[C/T]TTGGGAGGCTAGGGC	55884
rs537224256	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057104	TCCTGTCTCTTGGAG[C/T]CTGGGCCCAAACTAA	55884
rs537296229	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063640	TAAAAAAGGCATATG[A/T]TAACCTCAGAACTAA	55884
rs537381274	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048215	ATTACAGGCGTGAGC[C/T]ACCGCACCCGGCCAT	55884
rs537383320	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055683	GCAATGGCACAATCT[C/T]GGCTCACTGCAACCT	55884
rs537418673	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058847	GATTACAGGTATGCA[C/G]CACCACGCCTGGTTA	55884
rs537464293	in-del	-/CA	0.00246812	0.0350424	intron-variant	WSB2	GRCh38.p7	12:118034618	CTTTCTAAATCTGAC[-/CA]CAGTTAGTTCAAAAG	55884
rs537516042	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039194	GAGTCACTAGGGGCA[C/T]ACATTCTAGAGTCAG	55884
rs537821639	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051998	AAATAAAGTAAGACT[A/G]ATGATGGTGATGGAT	55884
rs537909973	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057629	ATGGAATATAACATG[C/T]TTTGATATATGTATA	55884
rs538064699	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038932	GTGCTGATCACTTTT[G/T]TTATATAATCTTGAA	55884
rs538176114	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037930	TTGAATGGGAAATCC[A/G]AATTAGAGGGATTCA	55884
rs538206158	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062700	TGTGTCCCGTTTGGC[C/T]TCCTGGGTTACACTC	55884
rs538387833	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047312	AGTTTGCTAATGAAT[C/T]AAGGGATGAGTTACG	55884
rs538472874	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118060811	TCCCGATCCTGTCGC[C/T]GGCGGGAGTCAGGGT	55884
rs538504475	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052094	TATAAATTACATCTC[A/C]ATAAAGCTATGGGAA	55884
rs538577845	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118045068	TTTTGTCAATTGTGT[A/G]GTGAAATACACAAAA	55884
rs538671798	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055763	GGGATTACAGGCGTG[C/T]ACCACCACACCCAGC	55884
rs538711909	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062668	CCCTGTTTTATGAGC[A/C]CTGGGTACGTCCTTC	55884
rs538845478	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118053232	CCATCTGCCCCAGCC[C/T]ATCGGTCCAACCTCC	55884
rs538964267	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118052085	TGTGTGGTATATAAA[C/T]TACATCTCAATAAAG	55884
rs539001850	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056252	GCCCTTCTCTCTACC[C/T]TCTGCCAATGCTCAA	55884
rs539015180	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049185	TTAGTAAACAATGTA[C/T]GACCTTGGCATTATC	55884
rs539214663	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118062003	AGAACACGGGGCGGT[G/T]GGGAGAGGAGGGCAG	55884
rs539228233	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036618	GCCCTGCAGCCAGGG[C/T]TGATTCTCTATCCCT	55884
rs539327575	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118048464	GTGTGGTGGCACACG[A/C]CTGTAATCCCAGTTA	55884
rs539417721	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038741	ACTAGAATACAGTGG[C/T]GCGATCTCAGCTCAC	55884
rs539454407	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118044699	TAAAACATGAGGCCC[C/T]GGCCACCACTGCGCC	55884
rs539454513	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037988	TTCACATGTGGGCTG[C/T]AACTTTTAAAATCTT	55884
rs539649431	snp	G/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118042688	GGGGCGGGCAGGGGC[G/T]ATTAGGAAAAAACTG	55884
rs539786662	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042406	ACAGGAGAGCCCACG[A/G]CAAAGGGTTATCCAG	55884
rs539786825	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049741	TGATGCATTTTGCCA[A/G]GCTTCCTTCCAAAAA	55884
rs539790170	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057125	CCCAAACTAAACTTG[A/G]CTACACGGAGAGAAA	55884
rs540110826	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118042194	AATTATTCTAGGCTT[-/A]AGAGTCTGCTTCAAA	55884
rs540117137	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057330	CCCAGGCTGGAGTGC[A/G]GTGGCGCCATCTCGG	55884
rs540202432	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039083	AGTGTTTATCTTCAT[C/T]TAAACTCTGTAATGG	55884
rs540405459	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051611	CCTGGAGAGTGCAGG[A/G]GGGTTGGGGGATCTA	55884
rs540590496	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118058165	CAGAGATGAAAGCTA[C/T]GACCCCAGCCAGCAG	55884
rs540621991	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061449	GGATAAAACCCAGGG[G/T]TTGTGCGGGGTCCTG	55884
rs540640460	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047594	TTGGCAGGGTGTGGC[A/G]GCTACGCCTTTAGGA	55884
rs540754641	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034838	CACCGTTATTAGCAA[A/G]ATCGATCATTTGAGT	55884
rs540783980	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118037467	AGGTCAGGAGTTCAA[C/G]ACCAGCCTGGCTAAT	55884
rs540799294	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041044	ACACAGTGAGACTCC[A/G]TCTCAAGAAAAAACA	55884
rs540949838	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032423	CCATGAAATGTAAAC[A/G]TTGGCCAATCCATTC	55884
rs541155855	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118049061	GACAGATCTTCCATG[C/T]TGTGCTTTTTAAAAA	55884
rs541287831	snp	A/G	0.000187213	0.00967324	missense, upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062135	TCCCCGTCCCCCTGA[A/G]AAACCTGCTCTCCCT	55884
rs541401813	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036176	CACTGCACTCCAGCC[C/T]GGGTGACAGAGCGAG	55884
rs541438786	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035638	GATACATGATAATTA[C/T]AGGACTGCCTATTAT	55884
rs541620234	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118048818	AGAAATAGGATTCAG[-/A]AAAAAAAAATTGTTA	55884
rs541670637	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054390	AGCGAGACTCTGTCT[A/C]AAAAAAAAATTGGCT	55884
rs541796370	snp	A/C	0.0158469	0.0875917	intron-variant	WSB2	GRCh38.p7	12:118050644	ACCCTCTCTCTCTCT[A/C]AAAAAAAATAAATGA	55884
rs541812064	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058051	CCTGGCCCTGGATCA[A/G]GGTGTTCTAATTAAA	55884
rs542257834	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039965	TGGCTAGGCTGGTCT[C/G]GAACTCCTGACCTCG	55884
rs542356893	in-del	-/C	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118038471	CTGGGGTGGTAACAG[-/C]CCCCCAGCCCAGTAT	55884
rs542396687	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045963	ATTTGTCTCTCTGTG[C/T]CTAGTGCATTTCACT	55884
rs542426587	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052212	TTCCTGAACCATGAG[C/T]CACCTTCCCTCTCTC	55884
rs542465267	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058522	CACGCGCCTATAGTT[C/T]GGTATTTTTTGCAGA	55884
rs542559756	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043743	TAAGCCACCCCACCC[A/G]GCCACATAAGACTTT	55884
rs542608307	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033509	CTTGTATAATCTGAC[A/C]TACAAATTTGTCATT	55884
rs542803440	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118051067	AAAAAAAGAAAAAAA[A/G]AAAGAAAGAAAGAAA	55884
rs543007413	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054941	CCTAGCACTTTGGTA[A/G]GCCGAGATGGGATGA	55884
rs543019124	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047518	AAAATGTATAACTAC[C/G]CTAACTAGAATATAA	55884
rs543082034	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062248	CATGGAGGCTTTTCA[C/T]GCCTGAAAGACCCCA	55884
rs543094843	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053397	AGAAAAAAGTAATAA[C/T]CCCACCTAGATTCAC	55884
rs543224378	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034929	TCTTTCCTTAAAAAG[C/T]TCCATGGTATACTCA	55884
rs543269476	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059205	TTGAACACTTAGCAC[A/C]AAAAAAAATCTAAAA	55884
rs543390801	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041121	TCAGATGAGGATGCA[C/T]GTGCACTGCCTTAGT	55884
rs543394187	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	WSB2	GRCh38.p7	12:118063035	GGCTCCCCCCTCCCA[C/T]TTTTCTCTTCTCTAA	55884
rs543600492	snp	C/T	0.000220106	0.0104883	intron-variant	WSB2	GRCh38.p7	12:118036290	ATCCCAGGCAGGTTC[C/T]TCATCAGTCCCCCCA	55884
rs543623589	snp	A/G/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118049298	AATGGTAAAATTTTC[A/G/T]TAACCATCCTCTCAT	55884
rs543632682	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042503	CACCCCAAGAGGGTA[C/T]AAACTAGTTCTTGGT	55884
rs543667991	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118053829	CAAGGAATGTGGAAT[A/G]TGGAAGACTTTGACC	55884
rs543846999	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037621	TGCAGTAAGCCGAGA[C/T]TGCGTCATTGCACTC	55884
rs544106437	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056884	CCAGCCTGGGTGACA[C/G]AGCAAGACTCTGTCC	55884
rs544242637	snp	G/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118051518	AGCTAGTCAAAAAAG[G/T]CTACGTGTTGTATGA	55884
rs544272989	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058991	GTGAGCCACCCCGGC[A/G]CATTTGGTTGATATT	55884
rs544350322	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118059773	GGCCCTTTTAAAAAG[A/T]ATTCTACGGGTAACA	55884
rs544388199	snp	C/T	0.00636936	0.0560724	intron-variant	WSB2	GRCh38.p7	12:118057312	CAGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT	55884
rs544451693	snp	A/C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032350	AATATCTGATGGCCA[A/C/G]CCAGGCCTCAAACCA	55884
rs544621967	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058580	TGGTCTCAAACTCCT[A/G]AGCTCAAGTGATCTA	55884
rs544783358	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046480	TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAAT	55884
rs544822840	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046105	AGGCTGCTTTCACAC[C/T]GTGACAGCGGAGTTC	55884
rs544857698	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052803	AGGAATATGCTAGAC[A/G]GTGCTGATTATGGGG	55884
rs545003006	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118035451	GCATTGTGTGCCCCT[C/T]GTGGAAAAGCTTGGG	55884
rs545152439	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118054776	TTATATAAAATAGGT[-/G]TGTGTTCCTGAAGTT	55884
rs545315231	snp	A/G			intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118061191	GCTTCCCGTCACATG[A/G]CGGTGGGCGCGGGCG	55884
rs545343544	snp	C/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063536	TTTTTTTGGCAAGTT[C/T]GTTTTTCCAAGTCTT	55884
rs545402375	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041836	CTCAGCTCACTGCAA[C/T]TTCTGCCTCCCAGGT	55884
rs545426887	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041196	AAGCCCTAATCCCCA[A/G]TGTGATGGTATTAGG	55884
rs545435951	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048403	GACTGGCCTGGGCAA[C/G]ATGGTGAAAACTTGT	55884
rs545438794	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054746	ATAGGAAAATAATAA[C/G]ATAGGTATATCTTGT	55884
rs545501912	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056072	CCAGCTGCTCTCCCG[C/G]CTTCCCCTCTAGCCC	55884
rs545508789	snp	A/G			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063179	CGATGGCTCATGCCT[A/G]TAATCCCAGCACTTT	55884
rs545549452	snp	A/G			missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043217	CGGGCACTTGGGGGT[A/G]GTGGCGTGCCCAGAG	55884
rs545604067	snp	A/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118053432	AAGAAGCGTACCCTG[A/T]TCTCACACTATCAAA	55884
rs545823008	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035552	ACTTCCTTGTGCTAA[C/T]TTGCTTATGCAAAGT	55884
rs545835606	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063694	CATCTTAAAATGTAA[A/G]TAATGGAGAAGGAGC	55884
rs545924269	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118037333	CATCACTTTAAACCT[C/T]TGTGAGAAGCATTAA	55884
rs545955402	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036853	GTATGTGCTGATGAA[A/G]ACCTGAGCCAAGTGC	55884
rs545955635	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043623	TTAACTTTGTTTGTA[C/T]TTTTTGTAGGACGGA	55884
rs545987371	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118036158	AGTGATCCAAGATTG[C/T]GCCACTGCACTCCAG	55884
rs545998699	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118037616	GAGGTTGCAGTAAGC[C/T]GAGATTGCGTCATTG	55884
rs546134624	in-del	-/TTAA	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118034785	ATGACTTACAGATCT[-/TTAA]TTACATTTAGGTTAA	55884
rs546172263	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063785	CTTATTGCATCATAA[C/T]ACATTTTGCCTAGTA	55884
rs546409236	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039888	AGCTGGGATTACAGG[C/T]ATCTGCCACCATGCC	55884
rs546501556	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050843	GATCACCTGAGGTCA[C/G]GAGTTTGAGACCAGC	55884
rs546566168	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039448	TCGTGAAGATGTATG[A/G]TTCCATTTTTGTCAA	55884
rs546685424	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118056057	CCAGTAGGCAACCTT[A/C]CAGCTGCTCTCCCGG	55884
rs546700084	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045320	CAGTGAGCTGAGATC[A/G]CACCACTGCACTCCA	55884
rs546758234	snp	A/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118037675	CTCTGTCTAAAAAAA[A/T]AAAAAAAGAAAAGAA	55884
rs546801070	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118043896	CTAAGGCAGGTGGAT[C/T]GCCTGAGGTCTAGAA	55884
rs546838090	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043438	TCTATCAACTTTTCA[A/T]CCTGGGACACGTAAG	55884
rs546906451	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118043033	AGGTGTGCCTGCCAC[A/G]GCCACACCCCTTGGC	55884
rs547076076	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053699	ATGGCTGATGAAGCT[G/T]ATAAGTTAAAGGCCT	55884
rs547192171	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033640	AAGCTAAATTAATAC[C/T]TCATACCAAATGGCT	55884
rs547250613	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058274	CATCTTATCATTCAG[A/G]GATTGGTCCTCATGT	55884
rs547327935	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032601	GCCTCCTGAGTAGCC[A/G]GAACCACAGAACCAC	55884
rs547459751	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118051508	AAATGAAAGGAGCTA[G/T]TCAAAAAAGGCTACG	55884
rs547735290	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046903	CAGCCTCCTGAGTAG[C/T]TGGGACTACAGGCGC	55884
rs547992650	in-del	-/G	0.00993419	0.0697739	intron-variant	WSB2	GRCh38.p7	12:118035477	TGGGATTTGCACACT[-/G]GGGAAAAAAAAGGGT	55884
rs547994756	snp	A/G	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118047771	AATAAAAATAGTAGC[A/G]AAACATGGGAGAAAT	55884
rs547997709	snp	A/C	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041366	GGCAGCAGGTGCTCA[A/C]AGACACCAAAACTAC	55884
rs548034850	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040773	CTAGAGTAGGCCAGG[C/T]GCAGTGGCTCACGCC	55884
rs548167996	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051009	ATAAGCTGAGATCAT[A/G]CCACTGTACTCCAGC	55884
rs548181628	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042625	TAGCCTAAATAGACA[C/T]ACAGTATATGTTCGG	55884
rs548218845	snp	C/T	0.00676609	0.0577691	intron-variant	WSB2	GRCh38.p7	12:118049504	CCTCCCAGGTTCACG[C/T]GATTCTCCTACCTCA	55884
rs548319382	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118050512	TGGGCATGGTGGCGC[A/G]CCTGTAGTATCAGGT	55884
rs548432382	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055496	TCTGGGAGGCAGAGG[C/T]GGAAGAATTGCTTGA	55884
rs548508103	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036969	GGTGGATCACATGAG[G/T]CCAGGAGTTCAAGAC	55884
rs548663688	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064129	AATCCACTGTCAACA[A/G]GCTTGTGGATTTGGG	55884
rs548918765	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044500	ACTCACGATGTTGCA[A/C]CTGATTAATGAGGCT	55884
rs549124513	snp	A/C	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118040213	CTTCAGCTGTCAAAT[A/C]TCAGGGTGCTGGGAG	55884
rs549161277	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118046162	CCACAAAGCCTAAAC[C/T]ATTTATAGAAAAAGT	55884
rs549173254	in-del	-/AAAAA	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033548	ATGCACACCATTGTT[-/AAAAA]AAAAAAAAAAAAGCC	55884
rs549212902	snp	C/T	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118043972	AAAAAAAAAACAATT[C/T]GCCGGGCGTAGTGGC	55884
rs549285950	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050304	GAATGGGAGCTCACG[A/G]CATTCTGACACTGGG	55884
rs549305111	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053277	CCCTGCAGGCCACAC[C/T]CTGGCCACAAAATCT	55884
rs549357060	snp	A/C	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118047960	AAGAGACAGTGTCTT[A/C]CTGTTGCCCAGGCTG	55884
rs549395718	snp	A/G	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118054442	TTGTGAGGCCAAGGC[A/G]GGCAGATCACCTGAG	55884
rs549397267	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118047279	GGTATCCTGGCCTAA[C/T]GCTCAACAAATACTT	55884
rs549411241	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039680	GCCTGTACATGGTCA[C/T]ATATATGAATTTATT	55884
rs549432084	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053837	GTGGAATGTGGAAGA[C/G]TTTGACCCTGGCTGT	55884
rs549546226	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045471	GGGAGGCTGAGGTGG[A/G]TGGATCACCTGAGGT	55884
rs549562321	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048242	CCATATAGCCTGTTT[G/T]TTTTCAATAAGCCTC	55884
rs549614811	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060782	GGGGATCTCCTCCCG[C/T]AGAAGCCCGATCTTC	55884
rs549627720	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052509	ACATGCTTCAAACAC[A/C]CACCCCCTTGCTCCC	55884
rs549913318	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118058448	GACCTCCCCAGGCTC[A/T]GATGATCCTCCCATC	55884
rs550161560	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041479	TGACTAAGATACAAG[C/T]TTTCAGGCTCATTGC	55884
rs550333090	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035932	TGAACCAGGCCAGGC[G/T]CAGTGGCTCATGCCT	55884
rs550365677	snp	C/G	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118041984	TGGTCTTGAACTCCT[C/G]ACCTCAGGTGATCCA	55884
rs550521129	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118047729	GCCCCCCAAAAAGCC[C/T]GATTATTTTAAATTA	55884
rs550650687	snp	A/G	8.53672e-05	0.00653271	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043322	CTTTTGGGCTGCCCC[A/G]CCCTTTCGTCTCATT	55884
rs550697606	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118041638	CAGCCCCTGATCCTC[G/T]TCATGACCCTTTACC	55884
rs550724850	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061793	GGGGCGGGAGAAATA[C/G]GTTGGAGGGAATACT	55884
rs550756611	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058125	TATTATAAGCCTCTT[C/G]TAGGCAAAGCAGTTA	55884
rs550789008	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050224	AACCAAGGCTGGCTG[A/T]ATGAATAAATACAGA	55884
rs550825062	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118049695	GGCATCAGGTACCGC[A/G]CCCAGCCCAGAAGAA	55884
rs550856322	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063364	ATCACTTGAACCCAG[A/G]AGGTGGAGGTTGCAG	55884
rs551288277	in-del	-/T	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118054687	TGTCTCAAAAAATAA[-/T]AATAATAATAATAAT	55884
rs551306551	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039379	TTGGAATTAGAGAGA[C/G]ATTTTCCATGGGGTA	55884
rs551351918	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052583	GAGCCACACTATCCA[C/T]TCCCAGAGGGAGTTG	55884
rs551608616	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038650	TCTATAAGATCAGTA[A/G]GGGTGAAGGGGTACA	55884
rs551739336	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042118	TTCCTTATTGGGCCA[C/G]CCCTGTATATAGTTT	55884
rs551744417	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118053041	CTGTCTGGGGTTAAA[C/T]CTTCATCTCATCTCA	55884
rs551814822	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118048040	CAGGTGATCCTCCCA[C/T]CTCAGCCTCCTGAGT	55884
rs551877958	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118038560	TATGACCAGATTTGT[A/C]ATTTAAACACCTGTA	55884
rs551881564	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050511	CTGGGCATGGTGGCG[C/T]GCCTGTAGTATCAGG	55884
rs551893733	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033949	GCTGTTCATAACTGG[A/T]CTGAAAATTTAACGT	55884
rs551986811	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040240	GGAGTACTGAATAAA[C/T]TAAGGCATGTTAGGT	55884
rs552023430	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046246	CGGGCGGATCACTTG[A/G]GGTCGGGAGTTTGAG	55884
rs552118289	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061683	GAGGGCTGTGGGGGT[A/G]AGGGGAACCAAAGGG	55884
rs552126735	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053224	ACCACATGCCATCTG[C/T]CCCAGCCCATCGGTC	55884
rs552190119	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063975	GAAAAACAAGAAAAA[A/T]GTCAGTTGCAATGGA	55884
rs552698516	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118057309	AGACAGAGTCTCACT[C/G]TGCTGCCCAGGCTGG	55884
rs552923602	snp	C/G			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061557	ATAGAAACCGGAGTA[C/G]GGGAAGCCGGGCTCA	55884
rs552963620	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038743	TAGAATACAGTGGCG[C/T]GATCTCAGCTCACTG	55884
rs553139406	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118037395	CCTCAGGCCAGGCGC[A/G]GTGGCTCACGCCTGC	55884
rs553149988	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044100	CTCCAGCCTGGGGAA[C/T]GAAGGCAAAACTCTA	55884
rs553218449	snp	C/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118036632	GCTGATTCTCTATCC[C/G]TTTTCTACAGCTCTT	55884
rs553255126	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036159	GTGATCCAAGATTGC[A/G]CCACTGCACTCCAGC	55884
rs553265226	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042715	ACTGTCTAAAAGGCT[C/T]CTTAAGGGGCAATCA	55884
rs553327958	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118051351	AGCAGCACTATTTGT[A/G]ATAACCAAAACATGA	55884
rs553512738	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045589	TGGTGGCGCATGCCT[A/G]TAATCCCAGCTACTC	55884
rs553551534	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052652	CCACATTCCACCACG[G/T]TTACTCAATCCTGGC	55884
rs553676523	snp	A/C	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118057865	CCAGATTCAAGTGAT[A/C]CTCCCGCCTCAGCCT	55884
rs553717146	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046327	AACTAGCCAGGCCTG[C/G]TGGGGGGTGCCTATA	55884
rs553791125	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039901	GGTATCTGCCACCAT[A/G]CCCTGCTAATTTTTA	55884
rs553924044	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118049487	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAC	55884
rs554155598	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038940	CACTTTTTTTATATA[A/G]TCTTGAATTGCATTA	55884
rs554204521	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118035420	AAACTGCCCTGGCTA[C/T]AAAAGGGCTCAAGAT	55884
rs554246298	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061248	GAAACGGAGGGGGGG[G/T]GCGGACGGGATAAAA	55884
rs554283415	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060293	AATATCCTCTGACTT[C/T]CACGCTGTCTTCTGA	55884
rs554309249	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118039722	GGATGTATGGATCCA[C/T]AAAAATTAATATTTC	55884
rs554469013	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033236	AGTTGAAACCAGCTG[A/T]TTAATCCAATGAAGT	55884
rs554657138	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118043461	CACGTAAGACTTTTG[A/G]GGAGTGGAGGGAAGG	55884
rs554723911	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033692	TCAGAAGGGAGCCCA[A/G]GAAGAAAAGCACTTG	55884
rs554738576	snp	C/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041688	TCCAGCCCCTGAGCC[C/G]CATCCAGGGCTGGAG	55884
rs554769748	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049278	CTGCAAAAATATCAT[A/C]TGGAAATGGTAAAAT	55884
rs554777147	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048158	GATCTAGAACTCCTA[A/G]CCTCAAGTGATCCTC	55884
rs554784997	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055815	AGACAGGTTTTTGCT[A/G]TCTTGGCCAGGCTGG	55884
rs554823715	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062916	GCGCACCCCTTTTTT[G/T]GGGACTCCACTTTTA	55884
rs554884160	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060062	ACCTGCTCTGAAAAT[C/T]TCTCCTAAGGAAATT	55884
rs554887297	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037205	TAAAGGGTCAGAAGT[A/G]AAATCTGCGGCCACC	55884
rs554904037	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054042	GGTATCTTGGATTCA[A/G]TAAAACAGATGGTAG	55884
rs555041266	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118058459	GCTCAGATGATCCTC[C/G]CATCTCAGCCTCCCC	55884
rs555127812	snp	A/G			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063338	GCTACTCGGGAGACT[A/G]AGGCAGGAGAATCAC	55884

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