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
rs555256094	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118051235	GGAACCTGAATCCAC[C/T]GCTGGTGGGAAAGTA	55884
rs555480128	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057254	TCTTGGTGAAAAGGC[A/C]TATGAATCAGGGTTT	55884
rs555623743	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044308	GACACTCAGTTTTTC[C/T]CATGAGTAAGAAAGC	55884
rs555661128	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037159	TGCACTCCAGCTTGG[A/G]CGAAAGAGTAAGACT	55884
rs555678658	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038784	CTCCCAAGTTGAAGC[A/G]ATTCTCCTGCCTCAG	55884
rs555711078	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044930	AAACTCAATGCATAC[G/T]TAGTTGAACATCTTT	55884
rs555779643	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118042302	CCCTTCACAGGACAT[A/G]GGGACTTTTTTGCTT	55884
rs555844276	snp	C/G	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118053144	CACATCACATCATTT[C/G]TTTCAAATACATTAG	55884
rs555881905	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034082	TACATTCTATTCACA[A/G]TCCCAAAGAAATGCT	55884
rs555916748	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040402	AGTGATTTCCAGAGC[C/T]ACTGCATGGACCTTC	55884
rs555981492	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052787	GAGAGACAGCCAGAC[A/C]AGGAATATGCTAGAC	55884
rs556013180	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044367	CTTAGAGGCTGAATA[G/T]CCACCACTCTCCTGC	55884
rs556061712	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051941	ATTGCGCCATTGCAC[C/T]CCAGCCTAGGAGACA	55884
rs556098406	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051386	AACCCAATGTCCATC[A/G]ACTGATAAATGTACG	55884
rs556116223	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040800	CGCCTGTAATCCCAG[A/C]ACTTTAGGAAGCCCA	55884
rs556228690	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046051	GTCAATAAAGTTTTA[C/T]TGGAACGCAGCCACA	55884
rs556363977	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059781	TAAAAAGAATTCTAC[A/G]GGTAACACTCACTGA	55884
rs556390971	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061308	GAAAATCGGGGAGGC[A/G]GTACGCTGACGGGAT	55884
rs556592808	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061979	CGGTAATGGGAGAGG[A/G]AAGTGAGGAGAACAC	55884
rs556626593	in-del	-/AA/AAA			intron-variant	WSB2	GRCh38.p7	12:118045364	GCAAGACTCCATCTC[-/AA/AAA]AAAAAAAAAAAAGAA	55884
rs556628208	snp	A/T	0.00597247	0.0543191	intron-variant	WSB2	GRCh38.p7	12:118054681	AAACTCTGTCTCAAA[A/T]AATAATAATAATAAT	55884
rs556726702	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063159	AAGGGTAAGGTCGCG[A/G]GGCGCGATGGCTCAT	55884
rs556742550	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039935	ATTTTTAGTAGAGCC[A/G]GAGTTTCACCATGTT	55884
rs556797701	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041894	CGAGTAGCTGGGACT[A/G]CAGGCGCCCACCACC	55884
rs556933225	snp	C/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118041732	GCATTGCAATAAATT[C/G]CCCTCTCTTATGTCA	55884
rs556983091	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054259	AGCCAGACATGGTGG[C/T]GGGCACCTGCAGTCC	55884
rs556993004	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043515	AGTGACACAATCATG[C/G]CTCACTGCAGCCTCG	55884
rs557113251	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036100	CTAGCTACTCGGGAG[A/G]CTCAGGCAGCAGAAT	55884
rs557126074	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050534	GTATCAGGTACTTGG[A/G]AGGCTAGGGCAGGAG	55884
rs557129726	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043032	GAGGTGTGCCTGCCA[C/T]GGCCACACCCCTTGG	55884
rs557151729	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118042260	AGGGACTTCTAGATC[A/G]GTGGTTCTCAACCTG	55884
rs557304967	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057106	CTGTCTCTTGGAGTC[A/T]GGGCCCAAACTAAAC	55884
rs557783529	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045094	CAAAAGAATTTTAAC[C/T]GGCCGGGTGCGGTGG	55884
rs557820227	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052019	GGTGATGGATGCACA[A/G]CTCTGTGGATAGACT	55884
rs557897111	in-del	-/TCCA	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118045331	ATCGCACCACTGCAC[-/TCCA]TCCAGCCTGGGCAAC	55884
rs557985812	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118053744	TTGACCATTATGACT[A/G]TGATACTTACTAATA	55884
rs558048610	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	WSB2, RFC5	GRCh38.p7	12:118032980	TGTTTTTCTTCAAGC[A/G]ACAAAGGTGGTAGAG	55884
rs558189413	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040965	GAGACACAAGAATGA[C/G]TTGAACCTGGGAGGC	55884
rs558269699	snp	A/C			utr-variant-3-prime, intron-variant, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118032760	GTTGCCCAGGCTGAT[A/C]TTGAACTCCTGGGCT	55884
rs558328273	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118040477	TTTAAAAAGGCACTG[C/T]CAGCCGAGCGTGGTA	55884
rs558328420	snp	A/C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118047327	CAAGGGATGAGTTAC[A/C/G]TGAAAAGCAGGGAGG	55884
rs558365084	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046656	GCCCCTGAGTTTGTT[G/T]TCACGAGAAGCAGCA	55884
rs558383149	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118038987	AAACCATATCAAAGG[A/G]ACCTTTGATAGCAGA	55884
rs558404911	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039753	TTTTTTATTTTTTTT[A/T]ATTTTTTTGAGACAG	55884
rs558504911	snp	A/C	1.64768e-05	0.00287021	missense	WSB2	GRCh38.p7	12:118035275	ACACAGATCTCAGTG[A/C]GCTAATGTGGACGTC	55884
rs558547361	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053233	CATCTGCCCCAGCCC[A/C]TCGGTCCAACCTCCT	55884
rs558587498	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060122	GGACTCCCGGAATCA[A/G]TTCTAAATCTATCCC	55884
rs558636821	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062685	TGGGTACGTCCTTCC[C/T]GTGTCCCGTTTGGCC	55884
rs558675061	in-del	-/AAG	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118057068	GAATCCAGGAGCTAA[-/AAG]AAGAACAAACCCAGT	55884
rs558703494	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057360	GCTCATTGCAACCTC[C/T]GCCCCCTGGGTTCAA	55884
rs558711889	in-del	-/A	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063133	ATGTACACGTCATGG[-/A]AAAAGAATAAAAGGG	55884
rs558756069	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048406	TGGCCTGGGCAACAT[A/G]GTGAAAACTTGTCTC	55884
rs558772930	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118062071	ACGGGGCAGGAGCGA[C/T]TCGGAAGAAGACTGT	55884
rs558792128	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118057266	GGCCTATGAATCAGG[G/T]TTTCTTTGTTTTCTC	55884
rs558862426	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118059594	CCCTGCCCACACCCT[C/G]AAAACGAAGTTGTCA	55884
rs558947577	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118049200	TGACCTTGGCATTAT[C/T]ATTAAACTGACCACA	55884
rs559196153	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055331	CAGGACAGCCCCCAG[C/G]AAAGAATCATCTGGC	55884
rs559337598	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049488	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCACG	55884
rs559414714	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064077	AGATTTTTTTTAAAG[C/G]ACAGTGTAACAACTT	55884
rs559505479	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063198	TCCCAGCACTTTGGG[A/T]GGCCAAGGCGGGCAG	55884
rs559541691	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062336	CAGCTCATTGTCCCC[A/C]AAATGCCTCCCCTTA	55884
rs559582084	snp	C/G	0.00318978	0.0398085	intron-variant	WSB2	GRCh38.p7	12:118043080	GGGAGGCGACATAGT[C/G]AGAACATGCACCCGA	55884
rs559591879	snp	C/T	0.000164832	0.00907682	missense	WSB2	GRCh38.p7	12:118036376	GGTGTAGGGGTCCCA[C/T]ATAATCACATTGGTA	55884
rs559592900	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032535	TACCGTGACACGATC[A/G]TGGCTCGCTACAGCC	55884
rs559619725	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042599	TATACAATATATCTT[C/T]GATATTAAAATAGCC	55884
rs559673032	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118052651	GCCACATTCCACCAC[A/G]GTTACTCAATCCTGG	55884
rs559796035	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050110	GAGGCTGAGGCAGGA[A/G]GGAAGTGGAGGTTGC	55884
rs559914404	in-del	-/G	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118050348	AAAGAAAGAAAAACT[-/G]GTATTAGAAACTAAA	55884
rs559992806	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044397	CCTGATGAGTTCCCT[C/T]ATCACTAGCTTAGAA	55884
rs560128975	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051614	GGAGAGTGCAGGGGG[A/G]TTGGGGGATCTAAAT	55884
rs560156254	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045146	CTTTGGGAGGCCAAG[A/G]TGGGCAGATCACGAG	55884
rs560262050	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118038454	GACTGGAGAACGGGA[A/G]AACTGGGGTGGTAAC	55884
rs560325950	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046146	ACAGGGACCTTATGG[C/T]CCACAAAGCCTAAAC	55884
rs560335177	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043964	TCTACTAAAAAAAAA[A/C]AACAATTCGCCGGGC	55884
rs560653434	snp	A/C/G	3.29871e-05	0.00406112	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052453	GGGGCGCCCGGGCTT[A/C/G]AGTTCGGCCAGCAGC	55884
rs560746928	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034858	ATCATTTGAGTTTTA[C/T]ATAATCTTGAATTGC	55884
rs560783230	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	WSB2	GRCh38.p7	12:118034304	CCGGCATAAGTGCTT[C/T]AGTGAGGACAGGACC	55884
rs560815214	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040511	CATACCTGTAATCCC[A/T]GCACTTTGGGAGGCC	55884
rs560851811	snp	C/T	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118040195	AAAGGTCAATCATGG[C/T]TTCTTCAGCTGTCAA	55884
rs561125963	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118037750	CCTGGGCTGTACCAA[A/C]TGGTGAACTCTCAAC	55884
rs561191784	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042441	AAATATCCATAGTGC[C/T]GATGAGAAAACCTGT	55884
rs561227656	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054863	CATTCTCAGAGGTTC[A/T]ATGTGTAAATTTGGG	55884
rs561283890	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041862	CAGGTTCAAGTGATT[A/C]TCCTGCCTCAGCCTC	55884
rs561709106	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050765	AAGCACCTGAAAAGA[C/T]GCTCGGCCAGGTGTG	55884
rs561747684	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050209	AAAAAGAAACTACGC[A/G]ACCAAGGCTGGCTGA	55884
rs561792508	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058113	TGGAAAGGTATATAT[C/T]ATAAGCCTCTTCTAG	55884
rs561896824	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118040332	CTCATAATTGGCCTA[C/T]TCCATCCCGCCCACT	55884
rs562207054	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040341	GGCCTACTCCATCCC[A/G]CCCACTCTTGGTCAC	55884
rs562249451	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043772	TTAAATCCTAGAAAC[A/G]AGCTGGCCTTCGGTG	55884
rs562413062	snp	C/T	0.000152834	0.00874034	intron-variant	WSB2	GRCh38.p7	12:118052277	GAGTGTTTGGAAATG[C/T]GCCGGATGGGGCCCC	55884
rs562449937	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051731	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGTGG	55884
rs562452002	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058540	TATTTTTTGCAGAGA[A/T]GGGGTTTTGCCATGC	55884
rs562499933	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033514	ATAATCTGACATACA[A/G]ATTTGTCATTTCCTG	55884
rs562536519	snp	A/G	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118039354	TGGTATATCTACCCC[A/G]TTAATGCAGTTGGAA	55884
rs562772821	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044510	TTGCAACTGATTAAT[A/G]AGGCTCCTTCATTTA	55884
rs562977707	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053415	CACCTAGATTCACAA[C/G]TAAGAAGCGTACCCT	55884
rs563063224	in-del	-/TATT	0.171253	0.237274	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032701	GTTTTTTTGGCTATT[-/TATT]TATTTATTTTTTAAA	55884
rs563120084	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118052944	CCCCATCATCAAGGC[C/T]AAAAACGTTCAGCCC	55884
rs563142758	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060386	CCTGATCATACATGT[C/T]ACCAGGGATCAGCGT	55884
rs563228319	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058118	AGGTATATATTATAA[A/G]CCTCTTCTAGGCAAA	55884
rs563296703	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118052263	GGCAAAAGAACAAGG[A/G]GTGTTTGGAAATGCG	55884
rs563345096	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118054945	GCACTTTGGTAGGCC[A/G]AGATGGGATGATAGC	55884
rs563586548	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036819	CTGCTTCTGAGTCCT[G/T]TTTGCCAATAGGGTA	55884
rs563609696	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049422	TTTTTTTTTTTTTGA[A/G]ATGGAATCTCGCTCT	55884
rs563650154	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048731	ATTTTCCTTAGCTAA[C/T]AGTGAAAAGATATAT	55884
rs563800587	snp	A/C	0.00358779	0.0422022	intron-variant	WSB2	GRCh38.p7	12:118041985	GGTCTTGAACTCCTG[A/C]CCTCAGGTGATCCAC	55884
rs563834485	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118055907	GGTGTAAACCACCAC[A/G]TCTGTTTTTTTTTTT	55884
rs563915792	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038280	AAGCAATAACGCTGG[A/C]GACTCACCGACTTCT	55884
rs564105231	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044288	TTGATGAGTGGAAGG[A/G]AAAAGACACTCAGTT	55884
rs564181159	snp	C/G/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118050791	GTGTGGTGGCTCACA[C/G/T]CTGTAATCCCAACAC	55884
rs564321034	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050320	CATTCTGACACTGGG[A/G]CTTGTCCATCCCAAA	55884
rs564393623	snp	A/G	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118056891	GGGTGACAGAGCAAG[A/G]CTCTGTCCCCAAAAA	55884
rs564428669	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063932	CAGAATTGTGGAGGC[C/T]CCCTTCCCAGGCTCC	55884
rs564627687	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058200	CTAGGTGATTTTTCC[C/T]GTATCAGGACATGTA	55884
rs564800779	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039400	CCATGGGGTACCTAC[A/G]GTTTAATGAAAAATG	55884
rs564812675	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118046110	GCTTTCACACTGTGA[C/T]AGCGGAGTTCAACAG	55884
rs564887539	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118040379	TGGTCTTTCCTTCCA[A/G]GTCATCAAGTGATTT	55884
rs564920911	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033605	AGGAGCACGGCCTCT[C/G]AGTCCCCTGTAATTT	55884
rs564999843	snp	C/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118052838	AATAGCAAGGCCTTC[C/G]AATGCATTTCAGGTT	55884
rs565161300	snp	A/C	0.000230738	0.0107385	missense	WSB2	GRCh38.p7	12:118035077	TTTTCAGTTCCAGGG[A/C]CCAGATCCTGAGGAG	55884
rs565215605	snp	G/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061401	GGGGCAGGGGTGGGG[G/T]GAGCTGAGCGGAAAC	55884
rs565268507	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118035564	TAATTTGCTTATGCA[A/T]AGTAGGTCAGCCCTC	55884
rs565376402	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042136	CTGTATATAGTTTGC[C/T]CGAGGCAGAATTTCA	55884
rs565389822	snp	C/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118047719	CCTTTTCTCTGCCCC[C/G]CAAAAAGCCCGATTA	55884
rs565454672	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118060564	CAGATCAAAACTGAG[A/G]CGTGGGTGGCGGTGG	55884
rs565517926	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046866	AGCCTTGAACTCCAG[A/G]GCTCGAGCAGTCCTT	55884
rs565522434	snp	C/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118054345	ACAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC	55884
rs565692742	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056935	AAAGCCCCTTAAACT[C/G]TGATGATGCTTATGC	55884
rs565782215	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048099	GCCAGGCTAATTTTT[A/C]AAACTTTTTTGTAGA	55884
rs565866866	snp	A/C	0.00835141	0.0640778	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063449	AGGAAAAAAAAAAAA[A/C]AAAAACAAAAAAGGC	55884
rs565995390	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048309	AATATGTGATTTTGC[C/T]AGGTGCAATGGCTCA	55884
rs566043233	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036069	TAGCCAGGCCTGGTG[G/T]CGCACGCTTGTAGTC	55884
rs566513178	in-del	-/CTTCTGAGTCTG	0.0111196	0.0737302	intron-variant	WSB2	GRCh38.p7	12:118036795	ACGCATGTGCAGAGA[-/CTTCTGAGTCTG]CTTCTGAGTCCTGTT	55884
rs566573086	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039665	AAATAATTGTTATAC[C/G]CCTGTACATGGTCAT	55884
rs566581135	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037697	AGAAAAGAAAAGAAA[A/C]GAAAACCCTCCAAAC	55884
rs566609900	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038759	GATCTCAGCTCACTG[C/T]AACCTCTGCCTCCCA	55884
rs566671144	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050507	TTGGCTGGGCATGGT[A/G]GCGCGCCTGTAGTAT	55884
rs566719779	snp	C/T	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118037135	TGCAGTGACCTGAGA[C/T]CACGTCACTGCACTC	55884
rs566867381	in-del	-/AT	0.316968	0.240864	intron-variant	WSB2	GRCh38.p7	12:118054683	ACTCTGTCTCAAAAA[-/AT]AATAATAATAATAAT	55884
rs566870616	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044825	TCTCCATGTGACCCT[A/G]ACCACACTCTGGTTG	55884
rs566877618	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053741	TTTTTGACCATTATG[A/T]CTGTGATACTTACTA	55884
rs566935110	in-del	-/A	0.00914312	0.0669923	intron-variant	WSB2	GRCh38.p7	12:118042733	AAGGGGCAATCACAG[-/A]AAAAAAACATCAAGA	55884
rs566935202	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045404	AGCTCATTTACAAAA[G/T]TAGAAGGGAGGGGCC	55884
rs567012408	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060749	AGTCCCACCCGGGAG[C/T]CCCCTCTGTCCCGGT	55884
rs567042940	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059634	AAAACCCCAGAACTG[G/T]AAACAGATTTCTGTT	55884
rs567082141	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058943	TCAAGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	55884
rs567139378	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051401	AACTGATAAATGTAC[A/G]AACAAAATTTGGCAT	55884
rs567195633	in-del	-/A	0.397994	0.201489	intron-variant	WSB2	GRCh38.p7	12:118055015	AGACTCCATCTCTTT[-/A]AAAAAAAAAAAAAAA	55884
rs567232488	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RFC5, WSB2	GRCh38.p7	12:118032615	CGGAACCACAGAACC[A/C]CAGGTAAATGCCACC	55884
rs567236281	in-del	-/A	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118059826	CTAGATGGGAAGGAG[-/A]AGAGAGCTGCCTTTA	55884
rs567355552	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053164	AAATACATTAGAAAG[C/T]TCCCGCCTGCCTACA	55884
rs567484487	snp	A/C			utr-variant-3-prime, downstream-variant-500B, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032238	TGCTGTTCTTTATAA[A/C]ATGTCAAATTCTTAA	55884
rs567622902	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061877	GGAAGGAAGGTGTAA[C/T]AACCGGGTGCTGGGG	55884
rs567767645	snp	A/G	1.65124e-05	0.00287331	intron-variant	WSB2	GRCh38.p7	12:118035186	AGCACTTGTTCTGAG[A/G]CCATGTAAAGAGAGT	55884
rs567806158	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041439	AAATAAATGTCTGTT[G/T]TTTAAGCCACCCAGT	55884
rs567966636	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046959	TAATTTTTGCAGAGA[C/T]AGGGTCTCACTATGC	55884
rs568155122	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118042236	TCTTTCTAACAGGAA[A/G]CACCCAACAGGGACT	55884
rs568160719	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118051058	CTCTGTCTCAAAAAA[A/G]GAAAAAAAAAAAGAA	55884
rs568197348	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118057555	GCTGGGATTGCAGGC[A/G]TGAGTCACCGCGTCC	55884
rs568199334	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118050521	TGGCGCGCCTGTAGT[A/G]TCAGGTACTTGGGAG	55884
rs568233717	snp	A/G	0.00993419	0.0697739	intron-variant	WSB2	GRCh38.p7	12:118057086	AAGAACAAACCCAGT[A/G]ACTCCTGTCTCTTGG	55884
rs568246692	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118048208	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC	55884
rs568291081	snp	C/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118048974	TACCCGGGAGCAGCT[C/G]TAGGTCATGTGACAG	55884
rs568345994	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055524	TGAGACCAGGAATTC[C/T]GGATCAAATGACCAG	55884
rs568383834	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118062540	CGCAGTGGTTCCATT[C/T]TAAATTTCTTTGCTT	55884
rs568721341	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058427	ATCACGGCTCACTGC[A/C]ACCTCGACCTCCCCA	55884
rs568917109	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118053634	TGGAGCTTCTTCATT[G/T]ACTGACCCACAGTTC	55884
rs569064303	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038605	TATTCTAATTCCCCA[C/T]GGAAACCAGTACCTA	55884
rs569177802	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062942	TTTTATCTCTGGCAC[C/T]AGTGTCGGCCTCCTC	55884
rs569261169	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039706	TTATTTAAGTTTATG[C/T]GGATGTATGGATCCA	55884
rs569263679	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033814	AGCCATCGTTCCCAG[C/T]GGAGGGAGTGTGAGC	55884
rs569304743	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040224	AAATCTCAGGGTGCT[A/G]GGAGTACTGAATAAA	55884
rs569359771	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118048011	AGCTCACTGCAGCCT[C/G]TAATTCCTGGGTGCA	55884
rs569397056	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118047303	AATACTTTGAGTTTG[C/T]TAATGAATCAAGGGA	55884
rs569398909	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118054469	TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA	55884
rs569518061	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118045500	GTCAGGAGTTCGAGA[C/G]CAGCCTGACCAATAT	55884
rs569553856	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058773	GAGATCTTGGTTCAC[C/T]GCAACCTCCACCTCT	55884
rs569794123	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118060784	GGATCTCCTCCCGCA[G/T]AAGCCCGATCTTCCC	55884
rs570063999	in-del	-/AT	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118051304	CTCAAATAGTTAAAC[-/AT]AGAAAACACAGGTTT	55884
rs570295403	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	WSB2	GRCh38.p7	12:118035228	CCTGTCATCTGCCAC[C/T]GTGGCAAGGTACAAG	55884
rs570746916	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049705	ACCGCGCCCAGCCCA[A/G]AAGAACATTTTTCAG	55884
rs570783791	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118049171	TTTCAGGTAGGGAAT[C/T]AGTAAACAATGTATG	55884
rs570874800	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118037975	AAGGAAATTTGGATT[C/T]ACATGTGGGCTGCAA	55884
rs570909831	snp	A/G	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118051795	CCTGGCCAACATGGC[A/G]AAACCTCGTCTCTAC	55884
rs570986534	in-del	-/TCCA	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118040375	CACTTGGTCTTTCCT[-/TCCA]AGTCATCAAGTGATT	55884
rs571022271	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041339	AGAGAGAAGGTGGCT[A/G]TTTACAAGCCAGGCA	55884
rs571106524	snp	A/T	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118052605	AGGGAGTTGTCACTT[A/T]AATGACCCAGGGCAA	55884
rs571151676	in-del	-/AT	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054747	TAGGAAAATAATAAC[-/AT]AGGTATATCTTGTTA	55884
rs571208614	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038665	AGGGTGAAGGGGTAC[A/G]TTGATCACTTTTTTG	55884
rs571243281	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118058885	ATTTTTAGTAGAGAC[A/G]GAGTTTCATTATGTT	55884
rs571466872	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118058553	GATGGGGTTTTGCCA[C/T]GCTGCCTAGACTGGT	55884
rs571863086	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118040484	AGGCACTGCCAGCCG[A/G]GCGTGGTACCTCATA	55884
rs571923441	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053061	ATCTCATCTCACCCA[A/G]ATCTTTTGCTACAGT	55884
rs571944998	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046286	GCCAACATGGTGATA[C/T]CCCATCTCTACTAAA	55884
rs571985581	snp	A/C	0.00557542	0.0525036	intron-variant	WSB2	GRCh38.p7	12:118045548	ACTAAAAATACAAAA[A/C]TTAGCTGGACGTGGT	55884
rs572009499	snp	A/G/T			intron-variant	WSB2	GRCh38.p7	12:118048964	CCCTTCCTTCTACCC[A/G/T]GGAGCAGCTCTAGGT	55884
rs572067248	snp	C/T	0.000214142	0.0103453	missense	WSB2	GRCh38.p7	12:118034206	GTTGCTTAAAAAGTC[C/T]TGTATGTGAGGAACT	55884
rs572310544	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118062096	GACTGTCCCCTTACC[C/T]ACCTACGGCGACAGC	55884
rs572448006	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061417	GAGCTGAGCGGAAAC[C/G]GGGTGGGGCGCGAAC	55884
rs572479181	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055783	CCACACCCAGCTAAT[C/T]TTTGTATTTTTAGTA	55884
rs572563915	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118041880	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	55884
rs572970489	snp	A/G	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118056717	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC	55884
rs573021372	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038118	CCTGTCTTTGGGTTC[A/G]TGTTAAAGTGCAAGT	55884
rs573079973	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033746	CACAGCAGGAGAGAA[C/T]TTGAACCAATGCTAC	55884
rs573138661	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062579	AACCTATGTTTTCTA[C/T]GGTAACTGAGGTTCC	55884
rs573158902	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036654	ACAGCTCTTCCAGAA[C/T]GTGTGGTGTAGGTTT	55884
rs573195798	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036170	TTGCGCCACTGCACT[C/G]CAGCCTGGGTGACAG	55884
rs573338021	in-del	-/T	0.00874735	0.0655527	intron-variant	WSB2	GRCh38.p7	12:118048238	CGGCCATATAGCCTG[-/T]TTTTTTTTCAATAAG	55884
rs573340675	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118044101	TCCAGCCTGGGGAAC[A/G]AAGGCAAAACTCTAT	55884
rs573467807	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118054642	AGATGGTGTCATTGC[A/G]CTCCAGCCTGGGCAA	55884
rs573487698	snp	A/T	0.0158469	0.0875917	intron-variant	WSB2	GRCh38.p7	12:118050643	GACCCTCTCTCTCTC[A/T]CAAAAAAAATAAATG	55884
rs573529794	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118040154	CTCCAGCCCATGCAA[C/T]ACAGTGAGACTCTGT	55884
rs573612644	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054323	TTGAACCCAGGAGGC[A/G]GAGGTTACAGTGAGC	55884
rs573630141	snp	A/G	0.00199481	0.0315187	intron-variant	WSB2	GRCh38.p7	12:118058025	TTCTCCTGCAGGCAT[A/G]AGCCATTGCACCTGG	55884
rs573711771	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052160	AATTGACTTTCACAT[A/G]TACAGAACTTGGGGC	55884
rs574040421	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118054053	TTCAATAAAACAGAT[A/G]GTAGAGATGCATATG	55884
rs574176472	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061250	AACGGAGGGGGGGTG[A/C]GGACGGGATAAAAAC	55884
rs574218634	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052579	CAAAGAGCCACACTA[C/T]CCATTCCCAGAGGGA	55884
rs574230914	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118049873	CTTATAAAAACCTTA[A/C]ATCTAATGTTATTTA	55884
rs574296014	snp	A/G	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118044532	CTTCATTTACTTCCT[A/G]ACTGATGGTAACCCG	55884
rs574392133	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033473	AGCCATCTGAATAGT[C/T]ATGCGGTTTAAGAAT	55884
rs574590451	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041701	CCCCATCCAGGGCTG[A/G]AGGAATTGAAAGATG	55884
rs574649971	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056464	TGATCGCCATCTGTC[C/T]CCCCTCCACTAGGAT	55884
rs574659653	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041080	ACCAAAAAAACACCT[A/G]GAGTTATCTTGGTGA	55884
rs574685059	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118037423	TGCAATCCCAGCACT[C/T]TGGGAGGCCCAGGCG	55884
rs574791198	snp	C/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118055857	TAGACTGAAGCAATC[C/G]GCCCACCTCGGACTC	55884
rs574840183	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118060241	CACCTTTCCCACTGA[G/T]ATTTTATGTTCATCT	55884
rs574879984	snp	C/G	0.00279162	0.0372561	intron-variant	WSB2	GRCh38.p7	12:118058733	TGGAGTTTCACTCTT[C/G]TTGCCCAGGCTGGAG	55884
rs574963818	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063394	GTGAGCTGAGATCTT[A/G]CCATTGCACACCAGC	55884
rs575067658	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	WSB2	GRCh38.p7	12:118063002	CCTGCCTCCTGAGGA[C/T]CCCCGTTTTATTGTC	55884
rs575410504	snp	C/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118057920	TACCACCACACTCAG[C/T]ATTTTTTTTTTTTTT	55884
rs575445879	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118057257	TGGTGAAAAGGCCTA[C/T]GAATCAGGGTTTCTT	55884
rs575498848	snp	C/T	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118037160	GCACTCCAGCTTGGG[C/T]GAAAGAGTAAGACTG	55884
rs575577354	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063949	CCTTCCCAGGCTCCA[C/T]CAGGGTTTGAGAAAA	55884
rs575792544	snp	A/C	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118053179	CTCCCGCCTGCCTAC[A/C]TCATAAAGGCAACTG	55884
rs575792865	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118046057	AAAGTTTTATTGGAA[C/T]GCAGCCACAGGCATT	55884
rs575835132	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118038880	GAGACAGGGTTTCAC[C/T]ATATTGGCCAGGCTG	55884
rs575860327	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045648	GCCAGGAGGCGGAGG[C/T]TGCACTGAGCCAAGA	55884
rs576081700	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039989	GACCTCGAGTGATCC[A/G]CCCGCCTTGGCCTCC	55884
rs576488518	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061997	GTGAGGAGAACACGG[G/T]GCGGTGGGGAGAGGA	55884
rs576600079	snp	A/G	0.0023933	0.0345097	intron-variant	WSB2	GRCh38.p7	12:118047617	CTTTAGGAAGCTGAG[A/G]TGGGAGGATCACTTG	55884
rs576665604	snp	A/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118034719	GGTTTCCCATATATT[A/T]TGCATCATCTCAATT	55884
rs576727023	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063682	CTCCCCCCACCACAT[C/T]TTAAAATGTAAATAA	55884
rs576735904	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118056066	AACCTTCCAGCTGCT[C/T]TCCCGGCTTCCCCTC	55884
rs576774668	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063174	GGGCGCGATGGCTCA[C/T]GCCTGTAATCCCAGC	55884
rs576938060	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118043529	GGCTCACTGCAGCCT[C/T]GACCTCCCTGTTCAA	55884
rs577001777	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118036156	GCAGTGATCCAAGAT[G/T]GCGCCACTGCACTCC	55884
rs577108685	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118050068	AGCTAGGGGTGGTGG[C/T]GCATGCCTGTAATCC	55884
rs577133730	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059832	TGGGAAGGAGAGAGA[A/G]CTGCCTTTAACTCAA	55884
rs577222198	snp	A/G	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118041744	ATTCCCCTCTCTTAT[A/G]TCACTTTTTTTTTTT	55884
rs577600276	in-del	-/TATTTATT	0.0074675	0.0606464	downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032697	CTAAGTTTTTTTGGC[-/TATTTATT]TATTTATTTTTTAAA	55884
rs577657678	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118052049	TAAAAGCCACTGTAT[C/T]GTATACTTAAATGGA	55884
rs577664286	snp	C/T	0.000798403	0.0199641	intron-variant	WSB2	GRCh38.p7	12:118045098	AGAATTTTAACTGGC[C/T]GGGTGCGGTGGCTCA	55884
rs577694104	snp	G/T	0.00159617	0.0282053	intron-variant	WSB2	GRCh38.p7	12:118058481	AGCCTCCCCAGTAGC[G/T]GGGACTACAGGCACA	55884
rs577838566	in-del	-/T	0.00119737	0.0244387	intron-variant	WSB2	GRCh38.p7	12:118037183	TAAGACTGTCTCAAA[-/T]TTTTTTTAAAGGGTC	55884
rs577964738	snp	G/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118059050	TTATTGTCTGTCTCT[G/T]TCTGAACCCACCCAA	55884
rs578158454	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	WSB2, RFC5	GRCh38.p7	12:118033058	CCATAAAGCACCGAT[C/T]AAGAAAGCTAAAGAA	55884
rs578244190	snp	C/T	0.000399281	0.0141238	intron-variant	WSB2	GRCh38.p7	12:118039827	CGGCTCACTGCAACC[C/T]CTGCCTCCTGGGTTC	55884
rs745473372	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118054853	AGAGACTATTCATTC[G/T]CAGAGGTTCTATGTG	55884
rs745656332	snp	A/G	1.65113e-05	0.00287322	intron-variant	WSB2	GRCh38.p7	12:118042984	AGCCCTGGCATGGGA[A/G]CAGGGGCACTGAGTC	55884
rs745723860	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044443	GAAAATAAACTCATC[C/T]TGCCAACACCGTTTG	55884
rs745731845	snp	A/G	1.65334e-05	0.00287514	intron-variant	WSB2	GRCh38.p7	12:118034970	CCACCCATCTGTTCA[A/G]CTAACAAATACATAC	55884
rs745760279	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118034893	AAGCTTTCCTCATAG[G/T]CAAGAAAATTCTAGA	55884
rs745822746	snp	A/C/T	1.64833e-05	0.00287078	missense	WSB2	GRCh38.p7	12:118036378	TGTAGGGGTCCCACA[A/C/T]AATCACATTGGTATC	55884
rs745920751	snp	G/T	1.67677e-05	0.00289544	intron-variant	WSB2	GRCh38.p7	12:118052519	AACACACACCCCCTT[G/T]CTCCCTGACCACCCA	55884
rs745959885	snp	A/C/T			intron-variant	WSB2	GRCh38.p7	12:118058328	CCTCACTATCTAAAG[A/C/T]GACCATACACTTTCC	55884
rs746175108	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118035914	GGCATCACTAAGAAG[A/C]AATGAACCAGGCCAG	55884
rs746232396	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038138	AAAGTGCAAGTCACA[A/G]GGGACTTTTGCAGGT	55884
rs746329003	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064033	ATAAATAGATCTCAT[A/G]GTCTCTAAGTTAACA	55884
rs746414800	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049433	TTGAGATGGAATCTC[A/G]CTCTGTTACCCAGGC	55884
rs746539522	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118047928	GGTTTTACAAACTGC[-/TT]TTTTTTTTGTTTTTT	55884
rs746582948	snp	A/C/G/T	4.96746e-05	0.00498352	intron-variant	WSB2	GRCh38.p7	12:118034391	CCGATGCTAAGACAG[A/C/G/T]GCTTGGATGTTCATG	55884
rs746614512	snp	A/C	1.64746e-05	0.00287002	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043185	GAGTCCCGTAGCAAG[A/C]ACCAGGCAAGAGACA	55884
rs746670897	snp	C/T	1.65211e-05	0.00287407	intron-variant	WSB2	GRCh38.p7	12:118043003	GGGCACTGAGTCAGC[C/T]AGAGAGGGGGCACGA	55884
rs746696467	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118042638	CACACAGTATATGTT[C/T]GGTATTAAACTCTAT	55884
rs746810951	snp	A/G	3.29609e-05	0.00405948	synonymous-codon	WSB2	GRCh38.p7	12:118035012	GACTCCACCATGTGG[A/G]AAAAATGTGCAGCAA	55884
rs746992813	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118054944	AGCACTTTGGTAGGC[C/G]GAGATGGGATGATAG	55884
rs747059967	snp	C/G	4.1377e-05	0.00454827	intron-variant	WSB2	GRCh38.p7	12:118038247	CACCACTTCAGACCT[C/G]CATGTCTCAGTGAAT	55884
rs747080018	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118047319	TAATGAATCAAGGGA[C/T]GAGTTACGTGAAAAG	55884
rs747308202	snp	A/G	8.60415e-05	0.00655846	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043330	CTGCCCCGCCCTTTC[A/G]TCTCATTTTTGCTAC	55884
rs747398141	in-del	-/AA			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063438	GCTCCGTCTGGAGGA[-/AA]AAAAAAAAAAAAAAA	55884
rs747422710	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118050729	AGACATTTATCCAAA[G/T]AACGTATACAAAGGA	55884
rs747489506	snp	C/T	3.29658e-05	0.00405978	missense	WSB2	GRCh38.p7	12:118035300	GACGTCACTGTCATC[C/T]ATGGCGGGGTCAACC	55884
rs747555031	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039515	CACAGGATTATACAA[A/G]TAGACAGAAAAATAT	55884
rs747656165	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051813	ACCTCGTCTCTACTA[A/G]TAATACAAAACTTAG	55884
rs747736569	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033375	GGTTTTTAGATAATC[A/G]AGAAAAACACAGTTG	55884
rs747772831	snp	A/G	1.65963e-05	0.0028806	intron-variant	WSB2	GRCh38.p7	12:118035134	ATATTAGCTGACCCA[A/G]GGCCAGACCAAGAGG	55884
rs747822435	snp	A/G	1.69444e-05	0.00291066	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043317	CTTCTCTTTTGGGCT[A/G]CCCCGCCCTTTCGTC	55884
rs747832884	in-del	-/AG			intron-variant	WSB2	GRCh38.p7	12:118036737	AAGGAGCTCACTATA[-/AG]AGAGAATAAACCAGA	55884
rs747974714	snp	C/T	0.000155426	0.00881412	intron-variant	WSB2	GRCh38.p7	12:118038423	AACAATGAGCCAGTC[C/T]TCAACAAAGCAGGAA	55884
rs748243520	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049104	GAATTTATAATTCAT[A/G]TAGTAAATTTACTTA	55884
rs748257814	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042866	CAGGTCCCAGATGCG[A/G]AGAGTCTTATCCCGT	55884
rs748269182	snp	A/G			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062614	TTCTTTTTCACCATG[A/G]TCTCTCCGTTTTAAT	55884
rs748354611	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118055608	TCCTCTACATTATCC[-/TT]TTTTTTTTTTTTTTT	55884
rs748421849	snp	A/T	3.29506e-05	0.00405884	missense	WSB2	GRCh38.p7	12:118034199	ATGTGGTGTTGCTTA[A/T]AAAGTCCTGTATGTG	55884
rs748596427	snp	C/G	1.64792e-05	0.00287042	synonymous-codon	WSB2	GRCh38.p7	12:118036388	CCACATAATCACATT[C/G]GTATCGTAAGAAGCC	55884
rs748682648	snp	C/T	1.67987e-05	0.00289811	intron-variant	WSB2	GRCh38.p7	12:118036317	CCCACAAAAAAGTCA[C/T]AGCAGGGATTCAGTC	55884
rs748723836	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041538	TGGCTGTGTGGAGCT[A/G]GACAGTCATAGCTTG	55884
rs748797166	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118041869	AAGTGATTCTCCTGC[C/T]TCAGCCTCCCGAGTA	55884
rs748861369	snp	C/T	3.295e-05	0.00405881	synonymous-codon	WSB2	GRCh38.p7	12:118036403	GGTATCGTAAGAAGC[C/T]GTGACAAGCAGGGCA	55884
rs748966165	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047600	GGGTGTGGCGGCTAC[A/G]CCTTTAGGAAGCTGA	55884
rs748989960	snp	A/G	3.2956e-05	0.00405918	synonymous-codon	WSB2	GRCh38.p7	12:118035288	TGAGCTAATGTGGAC[A/G]TCACTGTCATCCATG	55884
rs749061550	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118034663	AGTGCCACCTACTGA[A/C]TTATAGATGTTACCT	55884
rs749116250	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	WSB2	GRCh38.p7	12:118034214	AAAAGTCCTGTATGT[A/G]AGGAACTCTTTCATT	55884
rs749126558	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118059329	CTTTTTTTTAATGTG[A/G]CTACTTGAACATTTT	55884
rs749215668	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118046890	AGTCCTTCCATCTCA[A/G]CCTCCTGAGTAGCTG	55884
rs749263706	snp	A/G	1.64768e-05	0.00287021	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042882	AGAGTCTTATCCCGT[A/G]ACGCGGAGACCAAAA	55884
rs749367058	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038739	AGACTAGAATACAGT[A/G]GCGCGATCTCAGCTC	55884
rs749375520	snp	C/T	1.6522e-05	0.00287414	intron-variant	WSB2	GRCh38.p7	12:118034376	AAAATGAAACAGAAA[C/T]CGATGCTAAGACAGA	55884
rs749420020	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118056307	CCAACCATGCCCTTC[-/A]ACCTGGAATGCCTCT	55884
rs749466544	snp	A/G	1.65817e-05	0.00287933	missense	WSB2	GRCh38.p7	12:118036342	TCAGTCCTTACTGGA[A/G]TGACCTCAGCCTTTC	55884
rs749506636	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037874	TTTTCAATTAACAGG[A/G]TTTCAGGACAAAGTT	55884
rs749557473	snp	A/G	1.64838e-05	0.00287083	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052414	GCTCCAGGTTTCACA[A/G]CTGGACTTCCAATCA	55884
rs749844194	snp	A/G			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063113	AGTCTTACAGGCCTC[A/G]TTTTTATGTACACGT	55884
rs749945487	snp	A/G	4.95029e-05	0.00497484	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052467	TGAGTTCGGCCAGCA[A/G]CAGCGGTTCCTCTGG	55884
rs750000255	snp	C/T	1.65477e-05	0.00287638	missense	WSB2	GRCh38.p7	12:118036473	TGGCCCTCTAGCTTC[C/T]GAATTAACGTGTAGG	55884
rs750136114	snp	A/G	4.94442e-05	0.00497188	synonymous-codon	WSB2	GRCh38.p7	12:118036379	GTAGGGGTCCCACAT[A/G]ATCACATTGGTATCG	55884
rs750217575	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118050081	GGCGCATGCCTGTAA[A/T]CCCAGCTACTCAGGA	55884
rs750304066	snp	C/G	0.000247813	0.0111286	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043273	GGGCTGAAGGCCAGC[C/G]CCCAGACAATCTGAC	55884
rs750405602	snp	G/T	1.64743e-05	0.00287	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043169	TGATCTGCCCATCGT[G/T]GAGTCCCGTAGCAAG	55884
rs750567858	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118052612	TGTCACTTAAATGAC[C/T]CAGGGCAATAACAGC	55884
rs750783712	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118034047	AGATCCATGACTAGT[A/G]CACTGGAATCTGGTT	55884
rs750852854	snp	A/T	1.64792e-05	0.00287042	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034185	CAAAGAAGCACAAGA[A/T]GTGGTGTTGCTTAAA	55884
rs750874891	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118044725	GCGCCCAGGAAACAA[A/T]GTCTCAAATGCACAA	55884
rs750940948	snp	C/G	3.3248e-05	0.00407712	intron-variant	WSB2	GRCh38.p7	12:118042822	TGGAGTTGCCGAGTA[C/G]TTCCTTCACTTCCCA	55884
rs750969531	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044200	CCTGCAATGGGGTGA[C/T]CTGCCTTGTGGGATA	55884
rs750988945	snp	C/T			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032476	TGTTTTATGTGTTTA[C/T]TTTTTGAGGCAAGAT	55884
rs751103186	snp	A/G	1.66092e-05	0.00288172	synonymous-codon	WSB2	GRCh38.p7	12:118036484	CTTCCGAATTAACGT[A/G]TAGGACCTCATGCTC	55884
rs751198832	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118044803	TTTGCGGTACACAGC[A/T]CAAAGGTCTCCATGT	55884
rs751301258	snp	C/G	1.67435e-05	0.00289335	missense	WSB2	GRCh38.p7	12:118038298	CTCACCGACTTCTCT[C/G]CAGCTGCAGAGCACA	55884
rs751306909	snp	C/T	5.03554e-05	0.00501749	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043305	ACAGTCCAGCGTCTT[C/T]TCTTTTGGGCTGCCC	55884
rs751372901	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040059	GTGCCTGTAGTCCCA[A/G]CTACTCCAGAGACTG	55884
rs751388570	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050163	GCACTCCAGCCCGGG[C/T]GACAGAGCGAGACTC	55884
rs751498935	snp	A/G	1.65329e-05	0.0028751	intron-variant	WSB2	GRCh38.p7	12:118035107	GTCTGGATGGGGAGA[A/G]AGAACATCTGGATAT	55884
rs751562179	snp	A/G	1.79509e-05	0.00299585	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043375	TCAAACCCTTTAGGG[A/G]TGCTGGGAGAAGCAG	55884
rs751649287	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118037393	ACCCTCAGGCCAGGC[A/G]CGGTGGCTCACGCCT	55884
rs751681856	snp	A/C			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062461	ATTCCTTTCTCCCCG[A/C]CTTTCTTCGCTTCCC	55884
rs751709327	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118041289	CCTTAGAAGAAGAGA[C/T]ATGAAAGAGAGAGAT	55884
rs751709403	snp	A/G	1.65132e-05	0.00287339	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042842	TTCACTTCCCATACC[A/G]TGTTTATTCAGGTCC	55884
rs751799157	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118042368	AGAAGAGACCAGGCA[C/T]GCTGCTCAGTGTCTT	55884
rs751905316	snp	C/G	1.64874e-05	0.00287113	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042951	ACATCTTGGTGGCCG[C/G]AAAGATTCAAAAGCA	55884
rs751905390	snp	C/T	1.64779e-05	0.00287031	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034190	AAGCACAAGATGTGG[C/T]GTTGCTTAAAAAGTC	55884
rs752087366	in-del	-/A/AAAAAA			intron-variant	WSB2	GRCh38.p7	12:118037667	AGCGAAACTCTGTCT[-/A/AAAAAA]AAAAAAAAAAAAAAA	55884
rs752173598	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118036126	AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG	55884
rs752219451	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118042135	CCTGTATATAGTTTG[C/T]TCGAGGCAGAATTTC	55884
rs752281745	snp	A/G	1.8068e-05	0.00300561	intron-variant	WSB2	GRCh38.p7	12:118043392	GCTGGGAGAAGCAGA[A/G]ATTTCTTAATGAATC	55884
rs752284066	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118046593	TCACTTCGATCGGCT[G/T]CCTCTCCACAGACTG	55884
rs752337318	in-del	-/G	4.95741e-05	0.00497841	intron-variant	WSB2	GRCh38.p7	12:118043008	TGAGTCAGCCAGAGA[-/G]GGGGGCACGAGGTGT	55884
rs752369790	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047833	AATCCTAACACCACC[A/G]TTCTAAACGTCTCAC	55884
rs752372017	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118034535	AATTAAAGCTGCTGA[A/T]AGGATTAGAAAAACT	55884
rs752423016	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118052073	AAATGGACAAACTGT[A/G]TGGTATATAAATTAC	55884
rs752457905	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118060941	CAGCCCCCGCCCCAC[C/T]CCGCCCAGCCCGCCC	55884
rs752466225	snp	C/T	1.64876e-05	0.00287116	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034167	GGACGATTTACCCTG[C/T]TACAAAGAAGCACAA	55884
rs752672356	snp	A/C	1.66574e-05	0.0028859	intron-variant	WSB2	GRCh38.p7	12:118035353	AAACAGGATGGCAGG[A/C]CTGGAGTGATGGCTG	55884
rs752690318	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118041750	CTCTCTTATGTCACT[-/TT]TTTTTTTTTTTTTTT	55884
rs752697955	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118034889	CTTAAAGCTTTCCTC[A/C]TAGGCAAGAAAATTC	55884
rs752762627	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118060780	CGGGGGATCTCCTCC[C/T]GCAGAAGCCCGATCT	55884
rs752914591	snp	A/G	1.64993e-05	0.00287218	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042968	AAGATTCAAAAGCAG[A/G]AGCCCTGGCATGGGA	55884
rs753002816	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063872	TCCTGCGGCAATTAT[A/G]GGGCTTGTATGTGCT	55884
rs753089842	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055796	ATTTTTGTATTTTTA[A/G]TAGAGACAGGTTTTT	55884
rs753176620	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118043635	GTATTTTTTGTAGGA[C/T]GGAGTTTTGTCATGT	55884
rs753189965	snp	A/T	0.000125683	0.00792628	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062206	GACGCCCCCTTTTTA[A/T]CATTCCAGGGCCAGG	55884
rs753276067	snp	A/G	1.65652e-05	0.0028779	intron-variant	WSB2	GRCh38.p7	12:118052494	CTGGGGCAGGAGACA[A/G]CATGCTTCAAACACA	55884
rs753364137	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048750	GAAAAGATATATTCA[C/T]CTATACAAATTTATG	55884
rs753449809	snp	C/T	1.68835e-05	0.00290542	intron-variant	WSB2	GRCh38.p7	12:118035374	GTGATGGCTGCTCTC[C/T]ACCCTCCATCATCAC	55884
rs753578352	snp	A/C/T	4.95179e-05	0.00497563	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052324	CAACTGCTCCTCCAA[A/C/T]GGCCAGGGGATCAGT	55884
rs753615516	snp	A/G	1.64955e-05	0.00287184	synonymous-codon	WSB2	GRCh38.p7	12:118036364	CAGCCTTTCGCCGGT[A/G]TAGGGGTCCCACATA	55884
rs753646970	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048010	GAGCTCACTGCAGCC[C/T]CTAATTCCTGGGTGC	55884
rs753670682	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063723	GCTGCTTATTTTTCT[C/T]TGCAGCAGTTCCTGG	55884
rs753700587	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118036220	AGAGACCCACTGTGC[A/C]TTTTTATCCAGCTTG	55884
rs753736629	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118048911	CCACACTAGACCCTG[A/C]GCCACCCACAGTGCC	55884
rs753762782	snp	C/T	1.65023e-05	0.00287244	splice-acceptor-variant, intron-variant	WSB2	GRCh38.p7	12:118042974	CAAAAGCAGGAGCCC[C/T]GGCATGGGAGCAGGG	55884
rs753844373	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118051226	AGAGAATCTGGAACC[A/T]GAATCCACTGCTGGT	55884
rs753861413	snp	G/T			upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062239	AGGAGTCATCATGGA[G/T]GCTTTTCATGCCTGA	55884
rs753920450	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118057921	ACCACCACACTCAGC[-/A]TTTTTTTTTTTTTTA	55884
rs753932561	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118040127	ACAATAAGCCGAGAT[C/T]GCAGCATTGCACTCC	55884
rs753957866	snp	A/G	1.64825e-05	0.00287071	intron-variant	WSB2	GRCh38.p7	12:118043124	TTGTGCCAGCCAGGA[A/G]TGACCTACCTGTCTG	55884
rs754049741	snp	A/G	1.64773e-05	0.00287026	missense	WSB2	GRCh38.p7	12:118035061	GCAAATGCAATGGGA[A/G]TTTTCAGTTCCAGGG	55884
rs754049921	snp	A/G	4.97682e-05	0.00498815	intron-variant	WSB2	GRCh38.p7	12:118034951	GTATACTCAGCAGAA[A/G]GCACCACCCATCTGT	55884
rs754138879	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041293	AGAAGAAGAGACATG[A/G]AAGAGAGAGATCCCT	55884
rs754156594	snp	A/G	1.64969e-05	0.00287196	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043249	TTCCTGCTGGGTGGG[A/G]AAGGCCACGGGCTGA	55884
rs754189247	in-del	-/A	1.65689e-05	0.00287823	intron-variant	WSB2	GRCh38.p7	12:118052495	GGGGCAGGAGACAAC[-/A]ATGCTTCAAACACAC	55884
rs754230544	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118044661	CTACAATTCAACTTA[C/G]AGTGAAACAGGCCCA	55884
rs754260539	snp	A/T	1.6566e-05	0.00287797	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038323	AGCACAGCATGCTGC[A/T]GTCTGGGGAGATGGA	55884
rs754332768	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118056000	AAATCTAACCCCTCT[C/T]CATCTCTACTCTCAT	55884
rs754420603	snp	C/G/T			intron-variant	WSB2	GRCh38.p7	12:118043774	AAATCCTAGAAACAA[C/G/T]CTGGCCTTCGGTGAA	55884
rs754421578	snp	A/G	1.70525e-05	0.00291992	intron-variant	WSB2	GRCh38.p7	12:118036529	TGGAAAGTAAGAAGT[A/G]CCTGGTTAGGGCAGA	55884
rs754591325	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045081	GTGGTGAAATACACA[A/G]AAGAATTTTAACTGG	55884
rs754595287	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118058818	TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	55884
rs754604628	snp	A/G	1.69818e-05	0.00291387	intron-variant	WSB2	GRCh38.p7	12:118036523	GACCTGTGGAAAGTA[A/G]GAAGTGCCTGGTTAG	55884
rs754687066	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046411	GAGGTTGCAGTGAAC[C/T]GAGGTTGCACCACTG	55884
rs754713508	snp	A/G			utr-variant-3-prime	WSB2, RFC5	GRCh38.p7	12:118033116	TTTAAAATATATTAA[A/G]TTTTCCTAAGGCAGG	55884
rs754720181	snp	C/G	1.80335e-05	0.00300273	intron-variant	WSB2	GRCh38.p7	12:118043382	CTTTAGGGATGCTGG[C/G]AGAAGCAGAGATTTC	55884
rs754750224	snp	C/T	3.30885e-05	0.00406733	intron-variant	WSB2	GRCh38.p7	12:118035114	TGGGGAGAGAGAACA[C/T]CTGGATATTAGCTGA	55884
rs754879721	snp	C/G	1.64754e-05	0.00287009	missense	WSB2	GRCh38.p7	12:118035245	TGGCAAGGTACAAGC[C/G]TTCTGGAGAGAAGCA	55884
rs754928438	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118038600	TATGATATTCTAATT[C/T]CCCACGGAAACCAGT	55884
rs754984134	in-del	-/AT			intron-variant	WSB2	GRCh38.p7	12:118054685	CTGTCTCAAAAAATA[-/AT]ATAATAATAATAATA	55884
rs755006921	snp	C/G	1.70813e-05	0.00292239	intron-variant	WSB2	GRCh38.p7	12:118038414	AAAGAAGCAAACAAT[C/G]AGCCAGTCCTCAACA	55884
rs755038756	snp	A/G			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062581	CCTATGTTTTCTACG[A/G]TAACTGAGGTTCCCG	55884
rs755166958	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118056297	AGGCCTTTGCACCAA[C/T]CATGCCCTTCACCTG	55884
rs755309782	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	WSB2	GRCh38.p7	12:118034315	GCTTCAGTGAGGACA[A/G]GACCCTAGGAGCTGT	55884
rs755399702	snp	C/G	1.64942e-05	0.00287173	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042959	GTGGCCGGAAAGATT[C/G]AAAAGCAGGAGCCCT	55884
rs755524304	snp	A/G	0.000181337	0.00952028	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052345	GGGGATCAGTTTGAC[A/G]ATGCAGTGTCCTTGA	55884
rs755582838	snp	C/T	3.40565e-05	0.00412639	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043320	CTCTTTTGGGCTGCC[C/T]CGCCCTTTCGTCTCA	55884
rs755721286	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118037092	GAGGTTGAGGCAGAA[-/G]AATCACTTGAGCCTG	55884
rs755753149	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118047936	CAAACTGCTTTTTTT[G/T]GTTTTTTTAAGAGAC	55884
rs755774706	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047558	ATTCTCTCTTTTAAA[A/G]TACTTTTAAAATAGC	55884
rs755776264	in-del	-/G	1.7079e-05	0.00292219	intron-variant	WSB2	GRCh38.p7	12:118052260	ATGGCAAAAGAACAA[-/G]GGAGTGTTTGGAAAT	55884
rs755777268	snp	A/T	1.80935e-05	0.00300773	intron-variant	WSB2	GRCh38.p7	12:118043406	AGATTTCTTAATGAA[A/T]CTGCAATTGTTACCA	55884
rs755881831	snp	A/G	1.67801e-05	0.00289651	intron-variant	WSB2	GRCh38.p7	12:118035368	CCTGGAGTGATGGCT[A/G]CTCTCCACCCTCCAT	55884
rs755938709	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044546	TAACTGATGGTAACC[C/T]GCACAAGGATCAAAC	55884
rs755973915	snp	A/G	8.23839e-05	0.00641757	synonymous-codon	WSB2	GRCh38.p7	12:118035279	AGATCTCAGTGAGCT[A/G]ATGTGGACGTCACTG	55884
rs756056369	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058180	TGACCCCAGCCAGCA[A/G]GAAGCTAGGTGATTT	55884
rs756173373	snp	A/G	1.65015e-05	0.00287237	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042970	GATTCAAAAGCAGGA[A/G]CCCTGGCATGGGAGC	55884
rs756191937	snp	C/G	1.64814e-05	0.00287061	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042868	GGTCCCAGATGCGAA[C/G]AGTCTTATCCCGTGA	55884
rs756232566	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050171	GCCCGGGCGACAGAG[C/T]GAGACTCCATCTCAA	55884
rs756269708	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063873	CCTGCGGCAATTATG[A/G]GGCTTGTATGTGCTT	55884
rs756328867	in-del	-/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118063065	TTTTCTGAGTCTCCA[-/T]TTTTTTGTCTCCCAA	55884
rs756359973	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118049124	AAATTTACTTACATG[C/T]CAAGTCTAGAAATGA	55884
rs756396366	snp	C/T	1.65689e-05	0.00287823	intron-variant	WSB2	GRCh38.p7	12:118052495	TGGGGCAGGAGACAA[C/T]ATGCTTCAAACACAC	55884
rs756441286	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118043636	TATTTTTTGTAGGAC[A/G]GAGTTTTGTCATGTT	55884
rs756494714	snp	A/C	1.6617e-05	0.00288239	intron-variant	WSB2	GRCh38.p7	12:118034940	AAAGCTCCATGGTAT[A/C]CTCAGCAGAAAGCAC	55884
rs756503164	in-del	-/AAA			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063437	GGCTCCGTCTGGAGG[-/AAA]AAAAAAAAAAAAAAA	55884
rs756660139	snp	A/C	0.000412031	0.0143473	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062211	CCCCTTTTTAACATT[A/C]CAGGGCCAGGGCAGG	55884
rs756706012	snp	A/G	1.64784e-05	0.00287035	missense	WSB2	GRCh38.p7	12:118036389	CACATAATCACATTG[A/G]TATCGTAAGAAGCCG	55884
rs756733531	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118056061	TAGGCAACCTTCCAG[A/C]TGCTCTCCCGGCTTC	55884
rs756834666	snp	A/G	1.70904e-05	0.00292316	intron-variant	WSB2	GRCh38.p7	12:118052261	ATGGCAAAAGAACAA[A/G]GAGTGTTTGGAAATG	55884
rs756843136	snp	C/T	3.35132e-05	0.00409334	intron-variant	WSB2	GRCh38.p7	12:118042804	AAGCAAATACAGTAT[C/T]TTTGGAGTTGCCGAG	55884
rs756982128	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044304	AAAAGACACTCAGTT[C/T]TTCCCATGAGTAAGA	55884
rs757004162	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118054829	ATAAATCATATCAAG[C/G]CTTTGTAAAGAGACT	55884
rs757015369	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118036242	TCCAGCTTGTCCCCT[C/T]CCATGTCCCAGATTC	55884
rs757275778	snp	A/G	6.60333e-05	0.00574563	intron-variant	WSB2	GRCh38.p7	12:118042981	AGGAGCCCTGGCATG[A/G]GAGCAGGGGCACTGA	55884
rs757478575	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118039305	CTTTAAAAATAAAAA[A/C]GCCCGTCCATATAGA	55884
rs757481828	snp	A/C	3.29625e-05	0.00405958	intron-variant	WSB2	GRCh38.p7	12:118043128	GCCAGCCAGGAATGA[A/C]CTACCTGTCTGCACC	55884
rs757515142	snp	G/T	3.4408e-05	0.00414763	intron-variant	WSB2	GRCh38.p7	12:118036540	AAGTGCCTGGTTAGG[G/T]CAGAAGCAAAGTGCT	55884
rs757561303	in-del	-/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063632	TTATCTTTTAAAAAA[-/G]GCATATGATAACCTC	55884
rs757612275	snp	A/G			intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118061646	GAAGCGGCGATCCGG[A/G]GAGAACGGAGAGAGG	55884
rs757700971	snp	C/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032378	CCACCCAGAGGCTCA[C/G]CATCTGCTGTACCTG	55884
rs757793610	snp	C/T	3.29592e-05	0.00405938	missense	WSB2	GRCh38.p7	12:118036384	GGTCCCACATAATCA[C/T]ATTGGTATCGTAAGA	55884
rs757855158	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118044732	GGAAACAATGTCTCA[A/G]ATGCACAAGCACTTG	55884
rs757965840	snp	C/T	1.68801e-05	0.00290512	intron-variant	WSB2	GRCh38.p7	12:118036304	CCTCATCAGTCCCCC[C/T]ACAAAAAAGTCATAG	55884
rs758022060	snp	C/T	3.30109e-05	0.00406256	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052471	TTCGGCCAGCAGCAG[C/T]GGTTCCTCTGGGGCA	55884
rs758043510	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118056235	CCTGGCTCCAACACA[A/T]TGCCCTTCTCTCTAC	55884
rs758053164	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057584	CCAGCCTCTTCTTTT[C/T]TAAACTGATAAATAA	55884
rs758137333	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118043880	CCAGCACTTTGGGAG[G/T]CTAAGGCAGGTGGAT	55884
rs758168315	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043170	GATCTGCCCATCGTT[A/G]AGTCCCGTAGCAAGA	55884
rs758281992	snp	A/G	1.66233e-05	0.00288295	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043293	GACAATCTGACCACA[A/G]TCCAGCGTCTTCTCT	55884
rs758423211	snp	A/G	1.65031e-05	0.00287251	intron-variant	WSB2	GRCh38.p7	12:118034982	TCAGCTAACAAATAC[A/G]TACCCTGTGGCAATG	55884
rs758585332	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118040267	AGGTCAGTGGGGCAG[C/T]GCCTGTCAGCTGGGA	55884
rs758710414	snp	C/T			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032282	AAAAGTCACTATTCC[C/T]TTTGTTCATGGAGGA	55884
rs758713701	snp	C/T	1.66112e-05	0.00288189	intron-variant	WSB2	GRCh38.p7	12:118042825	AGTTGCCGAGTAGTT[C/T]CTTCACTTCCCATAC	55884
rs758741260	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118055609	CTCTACATTATCCTT[-/TT]TTTTTTTTTTTTTTT	55884
rs758781352	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118051487	GAACTGTGAAAACAT[C/T]ATGTAAAATGAAAGG	55884
rs758801638	snp	A/C	1.65888e-05	0.00287996	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038373	AGGTGGCCCGATAAC[A/C]CTTGAATCTGTTTAC	55884
rs758947412	snp	C/T	6.59141e-05	0.00574045	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034187	AAGAAGCACAAGATG[C/T]GGTGTTGCTTAAAAA	55884
rs758988539	snp	A/C			utr-variant-3-prime	WSB2	GRCh38.p7	12:118034088	CTATTCACAATCCCA[A/C]AGAAATGCTATTTCA	55884
rs759034471	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118038119	CTGTCTTTGGGTTCG[-/T]GTTAAAGTGCAAGTC	55884
rs759055348	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118047803	TGAAAATGAGACAAA[G/T]TAAAAATTACCTATA	55884
rs759057347	in-del	-/A	0.197531	0.244432	intron-variant	WSB2	GRCh38.p7	12:118036307	CATCAGTCCCCCCAC[-/A]AAAAAGTCATAGCAG	55884
rs759209052	snp	A/G	1.64914e-05	0.00287149	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034156	TCCCTTTGACAGGAC[A/G]ATTTACCCTGCTACA	55884
rs759293127	snp	A/G	1.67489e-05	0.00289381	intron-variant	WSB2	GRCh38.p7	12:118042808	AAATACAGTATTTTT[A/G]GAGTTGCCGAGTAGT	55884
rs759313603	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118058540	TATTTTTTGCAGAGA[-/T]GGGGTTTTGCCATGC	55884
rs759401258	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	WSB2	GRCh38.p7	12:118034244	TTTCTTGGGGATTGG[C/T]AGTGCTAGGACTTGG	55884
rs759535021	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118044318	TTTTCCCATGAGTAA[C/G]AAAGCATACTGCAGG	55884
rs759571250	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118052106	CTCAATAAAGCTATG[A/G]GAAAAAAAGCCAACT	55884
rs759599489	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118040117	GGCAGAGGCTACAAT[A/C]AGCCGAGATCGCAGC	55884
rs759726567	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118056987	TTCTTAAACACAAGC[C/G]CTACTCAGAATTCAC	55884
rs759835037	in-del	-/CAGGCCCTGCAGC			intron-variant	WSB2	GRCh38.p7	12:118036600	CCACCACCAAATCTG[-/CAGGCCCTGCAGC]CAGGGCTGATTCTCT	55884
rs759854797	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118043455	CTGGGACACGTAAGA[C/T]TTTTGGGGAGTGGAG	55884
rs759926319	snp	C/T	3.29815e-05	0.00406075	intron-variant	WSB2	GRCh38.p7	12:118043093	GTCAGAACATGCACC[C/T]GAGCCTCCCAGAACC	55884
rs759944291	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045230	TTAGCCGGGCGTGGT[A/G]GCGGGTGCCTGTAGT	55884
rs759983078	snp	A/G	3.29522e-05	0.00405894	missense	WSB2	GRCh38.p7	12:118035044	GCCCATTGGTCATAG[A/G]AGCAAATGCAATGGG	55884
rs760041221	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118035814	ATTGAGGCTTCATAA[C/T]GCTGATTCCGAAGAA	55884
rs760071172	snp	C/G/T	6.65706e-05	0.00576901	intron-variant	WSB2	GRCh38.p7	12:118034406	AGCTTGGATGTTCAT[C/G/T]TTTTCATGAGGATGA	55884
rs760162725	snp	A/C/G	6.66417e-05	0.00577211	intron-variant	WSB2	GRCh38.p7	12:118042817	ATTTTTGGAGTTGCC[A/C/G]AGTAGTTCCTTCACT	55884
rs760175175	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118037100	GGCAGAAGAATCACT[G/T]GAGCCTGGTAGGTGG	55884
rs760208697	snp	A/C	3.29527e-05	0.00405898	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042928	GTGTGAAGCTCAGAT[A/C]TCTCACGACATCTTG	55884
rs760235160	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118049810	GAGTACCCATCTCAA[A/C]AAACTCCTGTCAACA	55884
rs760239670	snp	A/G	3.29609e-05	0.00405948	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034181	GCTACAAAGAAGCAC[A/G]AGATGTGGTGTTGCT	55884
rs760295592	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118048706	GGTTAATACTCAAAT[A/C]CCTTTTTTCATTTTC	55884
rs760401465	in-del	-/TTT			intron-variant	WSB2	GRCh38.p7	12:118059308	ATTGTCACCTAGTTC[-/TTT]TTTCTTTTTTTTAAT	55884
rs760406844	snp	A/G	1.6473e-05	0.00286988	stop-gained	WSB2	GRCh38.p7	12:118034279	TTGTTAGGAAACTTC[A/G]AAGGGCTTTCCGGCA	55884
rs760443387	snp	A/G	6.59631e-05	0.00574258	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052447	CTGGTGGGGGCGCCC[A/G]GGCTTGAGTTCGGCC	55884
rs760487817	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040786	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	55884
rs760533303	snp	A/T	1.65299e-05	0.00287483	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052313	GAGAATACTTACAAC[A/T]GCTCCTCCAACGGCC	55884
rs760608509	snp	A/G	0.000393468	0.0140207	intron-variant, upstream-variant-2KB	WSB2	GRCh38.p7	12:118062069	AAACGGGGCAGGAGC[A/G]ATTCGGAAGAAGACT	55884
rs760659162	snp	A/G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033806	TAGGCAGAAGCCATC[A/G/T]TTCCCAGCGGAGGGA	55884
rs760714100	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118042215	CTGCTTCAAAAAGAA[A/T]GTCTTTCTTTCTAAC	55884
rs760800697	snp	C/T	1.64811e-05	0.00287059	missense	WSB2	GRCh38.p7	12:118036435	AGTCGGGGGAGAAGT[C/T]ACAAGAGACAACACT	55884
rs760815810	snp	A/G	6.5937e-05	0.00574144	intron-variant	WSB2	GRCh38.p7	12:118043111	GCCTCCCAGAACCTT[A/G]TGCCAGCCAGGAATG	55884
rs760985213	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118043792	GGCCTTCGGTGAAAT[C/T]TGCTGTGACTTTTCT	55884
rs760990002	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118040647	ACACCTGGAGGAGGC[G/T]CTGTCTCAAAAAAAA	55884
rs761020899	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118045960	AGTATTTGTCTCTCT[C/G]TGCCTAGTGCATTTC	55884
rs761071374	snp	A/C	1.64765e-05	0.00287019	missense	WSB2	GRCh38.p7	12:118035054	CATAGGAGCAAATGC[A/C]ATGGGAGTTTTCAGT	55884
rs761121665	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038163	GCAGGTGGTGGCCAT[A/G]GCCCACCAGCATGCC	55884
rs761163069	snp	A/G	1.64882e-05	0.00287121	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043239	TGCCCAGAGCTTCCT[A/G]CTGGGTGGGGAAGGC	55884
rs761327462	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118055863	GAAGCAATCCGCCCA[C/T]CTCGGACTCCCAAAG	55884
rs761328673	in-del	-/CCGT/CCGTCCTTCCTGTGTT			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062690	CGTCCTTCCTGTGTC[-/CCGT/CCGTCCTTCCTGTGTT]CCGTTTGGCCTCCTG	55884
rs761419402	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038228	ACACTCACACACACC[A/G]GGCCACCACTTCAGA	55884
rs761436488	in-del	-/TGTG/TGTGTCCCGTCCTTCA			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062684	TGGGTACGTCCTTCC[-/TGTG/TGTGTCCCGTCCTTCA]TGTGTCCCGTTTGGC	55884
rs761490694	snp	G/T	1.65269e-05	0.00287457	missense	WSB2	GRCh38.p7	12:118036468	TTTGATGGCCCTCTA[G/T]CTTCCGAATTAACGT	55884
rs761537318	snp	C/G	1.64969e-05	0.00287196	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052458	GCCCGGGCTTGAGTT[C/G]GGCCAGCAGCAGCGG	55884
rs761576567	snp	C/T	0.000188058	0.00969504	missense, upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062117	CGGCGACAGCCTCGC[C/T]TGTCCCCGTCCCCCT	55884
rs761837781	snp	A/G	2.01521e-05	0.00317422	intron-variant	WSB2	GRCh38.p7	12:118038259	CCTCCATGTCTCAGT[A/G]AATTAAAGCAATAAC	55884
rs761904232	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063745	AGTTCCTGGCCAGTC[C/T]CAACGTGAGAAATAT	55884
rs762077635	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033978	GTAAGGCTCTGTTGC[C/T]GTGCAAGTGGAATCT	55884
rs762127065	snp	C/T	1.73769e-05	0.00294757	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043340	CTTTCGTCTCATTTT[C/T]GCTACTTCGGCTTTT	55884
rs762163611	snp	A/G			missense	WSB2	GRCh38.p7	12:118035223	CGTTACCTGTCATCT[A/G]CCACCGTGGCAAGGT	55884
rs762272087	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118046229	ACTTTGGGAGGCTGA[A/G]GCGGGCGGATCACTT	55884
rs762325319	snp	C/T	1.64866e-05	0.00287106	intron-variant	WSB2	GRCh38.p7	12:118035208	AAAGAGAGTTCTCTT[C/T]GTTACCTGTCATCTG	55884
rs762437572	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118050753	CAAAGGACCAGTAAG[A/C]ACCTGAAAAGATGCT	55884
rs762463125	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058562	TTGCCATGCTGCCTA[A/G]ACTGGTCTCAAACTC	55884
rs762466374	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118044683	ACAGGCCCAGATAAG[A/C]TAAAACATGAGGCCC	55884
rs762649438	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039847	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	55884
rs762668888	snp	C/T	8.29731e-05	0.00644047	synonymous-codon	WSB2	GRCh38.p7	12:118036481	TAGCTTCCGAATTAA[C/T]GTGTAGGACCTCATG	55884
rs762716712	snp	A/C	1.69012e-05	0.00290694	missense	WSB2	GRCh38.p7	12:118038290	GCTGGAGACTCACCG[A/C]CTTCTCTCCAGCTGC	55884
rs762730100	in-del	-/C			intron-variant	WSB2	GRCh38.p7	12:118055605	CTTCCTCTACATTAT[-/C]CCTTTTTTTTTTTTT	55884
rs762739437	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118040496	CCGAGCGTGGTACCT[C/G]ATACCTGTAATCCCA	55884
rs762916772	in-del	-/C	1.65748e-05	0.00287874	intron-variant	WSB2	GRCh38.p7	12:118034958	CAGCAGAAAGCACCA[-/C]CCATCTGTTCAGCTA	55884
rs762917493	snp	A/G	3.31972e-05	0.004074	intron-variant	WSB2	GRCh38.p7	12:118052298	ATGGGGCCCCAGTAC[A/G]AGAATACTTACAACT	55884
rs762945854	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118055432	AGAGAAACATTTTCA[A/T]ATGACCTGGATGGCC	55884
rs763022454	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118042283	TCAACCTGGGGAGAC[C/G]TTGCCCTTCACAGGA	55884
rs763039882	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050147	CCGAGATCGCACCAT[C/T]GCACTCCAGCCCGGG	55884
rs763159456	snp	A/G	1.77197e-05	0.00297649	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043357	CTACTTCGGCTTTTG[A/G]CTTCAAACCCTTTAG	55884
rs763182008	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118036782	GACCCCTGCTGAAAC[A/G]CATGTGCAGAGACTT	55884
rs763212396	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048080	CACATGCACCTGCCA[C/T]CACGCCAGGCTAATT	55884
rs763218507	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118054084	TGTATATTTATAAAA[C/T]ATTTTTGCCAGGTGC	55884
rs763296549	snp	A/G	1.64904e-05	0.00287139	missense	WSB2	GRCh38.p7	12:118035313	TCCATGGCGGGGTCA[A/G]CCTGGGTGTGGCTGG	55884
rs763443886	snp	C/T	1.6473e-05	0.00286988	missense	WSB2	GRCh38.p7	12:118034290	CTTCGAAGGGCTTTC[C/T]GGCATAAGTGCTTCA	55884
rs763450621	snp	C/G	6.59217e-05	0.00574078	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042947	CACGACATCTTGGTG[C/G]CCGGAAAGATTCAAA	55884
rs763473827	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118046360	CCCAGCTACTCGGGA[A/G]GCTGAAGCAGGAGAA	55884
rs763533797	snp	A/G	8.23798e-05	0.00641741	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042935	GCTCAGATCTCTCAC[A/G]ACATCTTGGTGGCCG	55884
rs763625623	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038183	ACCAGCATGCCTTCT[A/G]TTGGGGTGGATTTGC	55884
rs763626482	snp	C/T	1.65181e-05	0.00287381	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052318	TACTTACAACTGCTC[C/T]TCCAACGGCCAGGGG	55884
rs763682338	snp	A/G	3.29598e-05	0.00405941	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034184	ACAAAGAAGCACAAG[A/G]TGTGGTGTTGCTTAA	55884
rs763687449	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118050653	CTCTCTCAAAAAAAA[-/T]AAATGAATAAAATAA	55884
rs763690791	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044155	TTAACACAGGCTATA[C/T]TGGCCATGGCTCAAT	55884
rs763796702	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118048710	AATACTCAAATACCT[G/T]TTTTCATTTTCCTTA	55884
rs763901403	snp	G/T	3.36706e-05	0.00410295	intron-variant	WSB2	GRCh38.p7	12:118035372	GAGTGATGGCTGCTC[G/T]CCACCCTCCATCATC	55884
rs763925412	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118042241	CTAACAGGAAGCACC[C/T]AACAGGGACTTCTAG	55884
rs763995989	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063606	ACTTACTTAAAAATA[A/G]CTTTATTCCATTATC	55884
rs764201866	snp	A/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032319	CCCTTAAGGACAGCG[A/G]CAAAGTATGAAGCTA	55884
rs764235292	in-del	-/AC			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063454	AAAAAAAAAAAAAAA[-/AC]AAAAAAGGCGGGGCT	55884
rs764416783	snp	A/C	1.64773e-05	0.00287026	synonymous-codon	WSB2	GRCh38.p7	12:118035060	AGCAAATGCAATGGG[A/C]GTTTTCAGTTCCAGG	55884
rs764587174	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118044586	GTCAAGAGAGAAAAC[A/G]AATTCACAGGGCTGT	55884
rs764698361	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057448	CCTGGCTAATTTTTG[C/T]ATTTTTAGTAGAGAT	55884
rs764772394	snp	A/G	1.65941e-05	0.00288041	intron-variant	WSB2	GRCh38.p7	12:118034400	AGACAGAGCTTGGAT[A/G]TTCATGTTTTCATGA	55884
rs764853364	snp	A/G	8.24817e-05	0.00642137	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052459	CCCGGGCTTGAGTTC[A/G]GCCAGCAGCAGCGGT	55884
rs764978984	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118037529	AAAAATTAGCCAGGC[G/T]TGGTGTAGCACGCCT	55884
rs765075770	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118048932	CCACAGTGCCCTTAG[A/G]GAGATGCAAGCCCAG	55884
rs765098048	snp	G/T	1.65386e-05	0.00287559	missense	WSB2	GRCh38.p7	12:118036471	GATGGCCCTCTAGCT[G/T]CCGAATTAACGTGTA	55884
rs765249908	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118052670	ACTCAATCCTGGCAC[A/T]CCTCACTGCTGGTTA	55884
rs765345901	snp	C/T	3.51685e-05	0.00419321	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043348	TCATTTTTGCTACTT[C/T]GGCTTTTGGCTTCAA	55884
rs765396411	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040828	CCAGGTAGGCAGATC[A/G]CTTGAGGTCAGGAGT	55884
rs765435058	in-del	-/AAT			intron-variant	WSB2	GRCh38.p7	12:118054691	TCAAAAAATAATAAT[-/AAT]AATAATAATAATAAT	55884
rs765435275	snp	A/G	1.65141e-05	0.00287346	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043266	AGGCCACGGGCTGAA[A/G]GCCAGCCCCCAGACA	55884
rs765580055	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118046330	TAGCCAGGCCTGGTG[A/G]GGGGTGCCTATAGTC	55884
rs765612547	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045495	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	55884
rs765725340	snp	A/C			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118034031	CATGCCAGGGAGAGA[A/C]AGATCCATGACTAGT	55884
rs765833900	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044711	CCCTGGCCACCACTG[C/T]GCCCAGGAAACAATG	55884
rs765927222	snp	A/G	0.000149332	0.00863965	missense	WSB2	GRCh38.p7	12:118036482	AGCTTCCGAATTAAC[A/G]TGTAGGACCTCATGC	55884
rs766016294	snp	A/T	0.000125889	0.00793276	upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062205	AGACGCCCCCTTTTT[A/T]ACATTCCAGGGCCAG	55884
rs766024003	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057680	AAGCTCATTACCATA[C/T]ATGCATTACCTCACA	55884
rs766128534	snp	C/G	1.68707e-05	0.00290432	missense	WSB2	GRCh38.p7	12:118038291	CTGGAGACTCACCGA[C/G]TTCTCTCCAGCTGCA	55884
rs766194417	snp	C/T	1.7887e-05	0.00299052	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043370	TGGCTTCAAACCCTT[C/T]AGGGATGCTGGGAGA	55884
rs766221300	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118051013	GCTGAGATCATGCCA[C/T]TGTACTCCAGCCTGA	55884
rs766221757	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118038564	ACCAGATTTGTCATT[A/T]AAACACCTGTAATCT	55884
rs766256018	in-del	-/C	1.69295e-05	0.00290937	intron-variant	WSB2	GRCh38.p7	12:118036289	AATCCCAGGCAGGTT[-/C]CTCATCAGTCCCCCC	55884
rs766285212	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118034580	TACCAAAGCGCTCTC[C/T]CTGTCTCTCTCTCGG	55884
rs766397606	snp	A/G	1.66763e-05	0.00288753	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043300	TGACCACAGTCCAGC[A/G]TCTTCTCTTTTGGGC	55884
rs766418280	snp	A/G	3.31318e-05	0.00406999	intron-variant	WSB2	GRCh38.p7	12:118035330	CTGGGTGTGGCTGGG[A/G]AGGAAAGAAACAGGA	55884
rs766442233	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118057922	CCACCACACTCAGCA[-/T]TTTTTTTTTTTTTAA	55884
rs766474376	snp	A/G	7.23903e-05	0.00601581	intron-variant	WSB2	GRCh38.p7	12:118043412	CTTAATGAATCTGCA[A/G]TTGTTACCAGTCTAT	55884
rs766504246	snp	C/T	3.31192e-05	0.00406921	intron-variant	WSB2	GRCh38.p7	12:118052303	GCCCCAGTACGAGAA[C/T]ACTTACAACTGCTCC	55884
rs766505517	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118054097	AATATTTTTGCCAGG[G/T]GCAGTGGCTCACATC	55884
rs766668778	snp	A/G	1.64852e-05	0.00287094	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042950	GACATCTTGGTGGCC[A/G]GAAAGATTCAAAAGC	55884
rs766702574	snp	C/T	1.64781e-05	0.00287033	missense	WSB2	GRCh38.p7	12:118035287	GTGAGCTAATGTGGA[C/T]GTCACTGTCATCCAT	55884
rs766898751	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118047678	TGATCATGCCACTGT[A/C]CTCCAGCCTGGGTGA	55884
rs766902724	snp	A/G	6.58913e-05	0.00573945	missense	WSB2	GRCh38.p7	12:118034312	AGTGCTTCAGTGAGG[A/G]CAGGACCCTAGGAGC	55884
rs766960906	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047809	TGAGACAAAGTAAAA[A/G]TTACCTATAATCCTA	55884
rs767046657	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048549	CGAGATGCGCCACTA[C/T]ACTCTGGCCTGGATG	55884
rs767069845	snp	C/T	1.6713e-05	0.00289072	intron-variant	WSB2	GRCh38.p7	12:118042813	CAGTATTTTTGGAGT[C/T]GCCGAGTAGTTCCTT	55884
rs767087585	in-del	-/A	1.65091e-05	0.00287303	intron-variant	WSB2	GRCh38.p7	12:118042981	GGAGCCCTGGCATGG[-/A]GAGCAGGGGCACTGA	55884
rs767125850	in-del	-/T			intron-variant	WSB2	GRCh38.p7	12:118036876	CCAAGTGCTATCTTA[-/T]TCCACTTAAAAATAA	55884
rs767157940	snp	G/T	1.65723e-05	0.00287852	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038320	CAGAGCACAGCATGC[G/T]GCAGTCTGGGGAGAT	55884
rs767158297	in-del	-/TT			intron-variant	WSB2	GRCh38.p7	12:118047209	TCTCCATTTTATGGG[-/TT]ATTAACTTTCCTGGG	55884
rs767191250	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033968	AAAATTTAACGTAAG[G/T]CTCTGTTGCCGTGCA	55884
rs767242892	snp	C/T	1.65477e-05	0.00287638	intron-variant	WSB2	GRCh38.p7	12:118052306	CCAGTACGAGAATAC[C/T]TACAACTGCTCCTCC	55884
rs767317293	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047040	GCCTCCCAAAGTGCT[A/G]AGATTACAGGCGTGT	55884
rs767351335	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118058904	TTTCATTATGTTGGT[A/G]AGGCTGGTCTCGAAC	55884
rs767355073	snp	A/C	1.6633e-05	0.00288378	intron-variant	WSB2	GRCh38.p7	12:118035349	AAAGAAACAGGATGG[A/C]AGGCCTGGAGTGATG	55884
rs767428120	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057903	ATCGGGCTACGGGGG[C/T]GTACCACCACACTCA	55884
rs767624762	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118043551	CCTGTTCAACTGATC[A/C]TCCTGCCTCAGATCC	55884
rs767750979	snp	A/G	1.6498e-05	0.00287206	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042966	GAAAGATTCAAAAGC[A/G]GGAGCCCTGGCATGG	55884
rs767798521	snp	C/T	1.64893e-05	0.0028713	intron-variant	WSB2	GRCh38.p7	12:118043097	GAACATGCACCCGAG[C/T]CTCCCAGAACCTTGT	55884
rs767812813	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118055759	AGCTGGGATTACAGG[C/T]GTGCACCACCACACC	55884
rs767857335	in-del	-/C			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033733	AAGCAACTCTGACCA[-/C]AGCAGGAGAGAACTT	55884
rs767895456	snp	C/T	1.64732e-05	0.0028699	missense	WSB2	GRCh38.p7	12:118034321	GTGAGGACAGGACCC[C/T]AGGAGCTGTCCAGAA	55884
rs768001950	snp	A/G	1.6476e-05	0.00287014	missense	WSB2	GRCh38.p7	12:118035046	CCATTGGTCATAGGA[A/G]CAAATGCAATGGGAG	55884
rs768121218	in-del	-/TC			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062842	TTTAGCATGCCCCGT[-/TC]TCTCTCTTCATTTTC	55884
rs768179325	snp	A/G	0.000115326	0.00759274	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043200	AACCAGGCAAGAGAC[A/G]TCGGGCACTTGGGGG	55884
rs768226722	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118059995	TGAAGCTTGAACTTG[A/G]CTGCAAGATTACCAT	55884
rs768240037	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050738	TCCAAAGAACGTATA[C/T]AAAGGACCAGTAAGC	55884
rs768369761	snp	A/G			missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043247	GCTTCCTGCTGGGTG[A/G]GGAAGGCCACGGGCT	55884
rs768371445	snp	A/T	1.64795e-05	0.00287045	synonymous-codon	WSB2	GRCh38.p7	12:118035018	ACCATGTGGAAAAAA[A/T]GTGCAGCAAAGCCCA	55884
rs768408616	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118054215	GTCTCTACTAAAAAT[-/A]CCAAAAAAAAAAAAA	55884
rs768566699	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055183	TTTCTATAGACCCAG[A/G]GTTCTCAACTGGGGG	55884
rs768574799	snp	C/T	1.64947e-05	0.00287177	synonymous-codon	WSB2	GRCh38.p7	12:118036454	AGAGACAACACTGCT[C/T]TGATGGCCCTCTAGC	55884
rs768772935	snp	A/G	2.05687e-05	0.00320686	intron-variant	WSB2	GRCh38.p7	12:118038249	CCACTTCAGACCTCC[A/G]TGTCTCAGTGAATTA	55884
rs768788822	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118047326	TCAAGGGATGAGTTA[C/T]GTGAAAAGCAGGGAG	55884
rs768871429	in-del	-/AGAG			intron-variant	WSB2	GRCh38.p7	12:118039372	AATGCAGTTGGAATT[-/AGAG]AGAGATTTTCCATGG	55884
rs769029649	snp	G/T	1.64844e-05	0.00287087	synonymous-codon	WSB2	GRCh38.p7	12:118035303	GTCACTGTCATCCAT[G/T]GCGGGGTCAACCTGG	55884
rs769107003	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118040297	AACCAACTTTATTCC[C/T]CTCCTCTCCTTGAAA	55884
rs769128657	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039703	AATTTATTTAAGTTT[A/G]TGCGGATGTATGGAT	55884
rs769162899	snp	A/T	1.72639e-05	0.00293796	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043333	CCCCGCCCTTTCGTC[A/T]CATTTTTGCTACTTC	55884
rs769272280	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118048130	AACCAAGTCTTGTTA[C/T]GTTGCCCATGCTGAT	55884
rs769453827	snp	C/T	1.66095e-05	0.00288175	intron-variant	WSB2	GRCh38.p7	12:118035137	TTAGCTGACCCAGGG[C/T]CAGACCAAGAGGGCC	55884
rs769593426	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033438	ATATGATGCTAATAA[A/G]TGGCCACTGATAACT	55884
rs769619575	in-del	-/AG	1.6507e-05	0.00287284	intron-variant	WSB2	GRCh38.p7	12:118034371	GTCCTAAAATGAAAC[-/AG]AAACCGATGCTAAGA	55884
rs769717186	snp	C/T	1.64743e-05	0.00287	synonymous-codon	WSB2	GRCh38.p7	12:118034205	TGTTGCTTAAAAAGT[C/T]CTGTATGTGAGGAAC	55884
rs769809793	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118046120	TGTGACAGCGGAGTT[A/C]AACAGTCAAGACAGG	55884
rs769908457	snp	C/G/T	1.65064e-05	0.00287279	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043257	GGGTGGGGAAGGCCA[C/G/T]GGGCTGAAGGCCAGC	55884
rs769995731	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118060100	AACTCGGGTCCTTCA[A/T]GACCTGGGACTCCCG	55884
rs770082332	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118047397	ATTGGCAGAATTTAG[C/G]TTCACTGAAGTTAAA	55884
rs770111131	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050139	GCAGTGAGCCGAGAT[C/T]GCACCATCGCACTCC	55884
rs770115903	snp	A/G	1.64776e-05	0.00287028	missense	WSB2	GRCh38.p7	12:118035229	CTGTCATCTGCCACC[A/G]TGGCAAGGTACAAGC	55884
rs770136073	snp	C/G	1.68136e-05	0.0028994	intron-variant	WSB2	GRCh38.p7	12:118052282	TTTGGAAATGCGCCG[C/G]ATGGGGCCCCAGTAC	55884
rs770203960	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118036702	TGGATTCTTGAGGAT[G/T]TAAAACAATGGGCAT	55884
rs770240745	snp	C/T	5.00764e-05	0.00500357	intron-variant	WSB2	GRCh38.p7	12:118036328	GTCATAGCAGGGATT[C/T]AGTCCTTACTGGAGT	55884
rs770242064	snp	A/G	3.29636e-05	0.00405964	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052396	ATCTGGGGAGAAGGC[A/G]ACGCTCCAGGTTTCA	55884
rs770328206	snp	A/G	4.94556e-05	0.00497246	synonymous-codon	WSB2	GRCh38.p7	12:118035306	ACTGTCATCCATGGC[A/G]GGGTCAACCTGGGTG	55884
rs770469774	snp	A/G	3.30458e-05	0.0040647	intron-variant	WSB2	GRCh38.p7	12:118035174	CCATTACTTGCAAGC[A/G]CTTGTTCTGAGGCCA	55884
rs770472484	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053264	TCCCTTGTCCCCTCC[C/T]TGCAGGCCACACTCT	55884
rs770594983	snp	G/T	0.000148467	0.00861461	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034145	ATTCCAGCAACTCCC[G/T]TTGACAGGACGATTT	55884
rs770688338	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118040507	ACCTCATACCTGTAA[G/T]CCCAGCACTTTGGGA	55884
rs770744494	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033607	GAGCACGGCCTCTGA[A/G]TCCCCTGTAATTTAG	55884
rs770850721	snp	A/G	1.64893e-05	0.0028713	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052438	CCAATCAAACTGGTG[A/G]GGGCGCCCGGGCTTG	55884
rs770871875	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046894	CTTCCATCTCAGCCT[C/T]CTGAGTAGCTGGGAC	55884
rs770882177	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118051990	AAATAAATAAATAAA[A/G]TAAGACTGATGATGG	55884
rs770916551	snp	C/T	8.23649e-05	0.00641683	missense	WSB2	GRCh38.p7	12:118034226	TGTGAGGAACTCTTT[C/T]ATTTTCTTGGGGATT	55884
rs770959744	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118034672	TACTGAATTATAGAT[A/G]TTACCTGTAAAGTGG	55884
rs770979160	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047866	TAAATTTTTGTGTAT[A/G]TACACAAATGTCTTT	55884
rs770983930	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118055435	GAAACATTTTCAAAT[A/G]ACCTGGATGGCCTGG	55884
rs771048773	snp	C/T	1.65778e-05	0.002879	synonymous-codon	WSB2	GRCh38.p7	12:118036343	CAGTCCTTACTGGAG[C/T]GACCTCAGCCTTTCG	55884
rs771172187	snp	A/C	3.34348e-05	0.00408855	intron-variant	WSB2	GRCh38.p7	12:118052511	ATGCTTCAAACACAC[A/C]CCCCCTTGCTCCCTG	55884
rs771214029	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118045192	CCACGGTGAAACCCC[G/T]TCTCTACTAAAAATA	55884
rs771224771	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118036791	TGAAACGCATGTGCA[C/G]AGACTTCTGAGTCTG	55884
rs771337820	in-del	-/AA	0.000135066	0.00821672	intron-variant	WSB2	GRCh38.p7	12:118036307	CATCAGTCCCCCCAC[-/AA]AAAAGTCATAGCAGG	55884
rs771353896	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118049265	CAAAATTTGATGGCT[A/G]CAAAAATATCATATG	55884
rs771403237	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118056942	CTTAAACTCTGATGA[A/T]GCTTATGCCAAACAT	55884
rs771416433	snp	C/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063162	GGTAAGGTCGCGGGG[C/T]GCGATGGCTCATGCC	55884
rs771429208	snp	C/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063534	ATTTTTTTTGGCAAG[C/T]TCGTTTTTCCAAGTC	55884
rs771744404	snp	A/G	1.64749e-05	0.00287005	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042913	TCAAACTGCCACTGG[A/G]TGTGAAGCTCAGATC	55884
rs771777990	in-del	-/ACAGCAGAG			cds-indel, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033255	ATCCAATGAAGTTAA[-/ACAGCAGAG]ACAGATCTCGTACAT	55884
rs771809505	snp	A/G	1.65121e-05	0.00287329	intron-variant	WSB2	GRCh38.p7	12:118042988	CTGGCATGGGAGCAG[A/G]GGCACTGAGTCAGCC	55884
rs771836387	snp	C/G/T			intron-variant	WSB2	GRCh38.p7	12:118053460	AAAACGGAAATAAGT[C/G/T]GCACCTTGTTTATTT	55884
rs771953194	snp	C/T	1.65332e-05	0.00287512	intron-variant	WSB2	GRCh38.p7	12:118034380	TGAAACAGAAACCGA[C/T]GCTAAGACAGAGCTT	55884
rs771996936	snp	A/C	4.94678e-05	0.00497307	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052444	AAACTGGTGGGGGCG[A/C]CCGGGCTTGAGTTCG	55884
rs772068681	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045845	TTATACCTTTGATCA[A/G]TATCTCCCCACTCCC	55884
rs772124498	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118044356	CTAGGGCAGAACTTA[G/T]AGGCTGAATATCCAC	55884
rs772167480	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118043501	CCAAGCTGGCGTACA[A/G]TGACACAATCATGGC	55884
rs772191141	snp	C/T	1.68414e-05	0.0029018	intron-variant	WSB2	GRCh38.p7	12:118052525	CACCCCCTTGCTCCC[C/T]GACCACCCAGACACA	55884
rs772410424	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118057070	ATCCAGGAGCTAAAA[A/G]AAGAACAAACCCAGT	55884
rs772414801	snp	A/C/G	4.94518e-05	0.00497231	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043229	GGTGGTGGCGTGCCC[A/C/G]GAGCTTCCTGCTGGG	55884
rs772448600	snp	A/C	1.7086e-05	0.00292279	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043323	TTTTGGGCTGCCCCG[A/C]CCTTTCGTCTCATTT	55884
rs772560392	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118040482	AAAGGCACTGCCAGC[C/T]GAGCGTGGTACCTCA	55884
rs772633787	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038157	ACTTTTGCAGGTGGT[A/G]GCCATGGCCCACCAG	55884
rs772859429	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118050854	GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT	55884
rs772928065	in-del	-/A	1.6625e-05	0.00288309	intron-variant	WSB2	GRCh38.p7	12:118034943	CTCCATGGTATACTC[-/A]AGCAGAAAGCACCAC	55884
rs772928345	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039813	CAATGGCATGATCCC[A/G]GCTCACTGCAACCTC	55884
rs772945289	snp	G/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033475	CCATCTGAATAGTCA[G/T]GCGGTTTAAGAATAC	55884
rs773013473	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118051834	CAAAACTTAGCCAGG[C/T]GTGGTGGTGTGTGCC	55884
rs773047994	snp	A/C	0.000187283	0.00967505	missense, upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062145	CCTGAGAAACCTGCT[A/C]TCCCTGTCTACCCGC	55884
rs773071261	snp	A/G	3.38708e-05	0.00411512	missense	WSB2	GRCh38.p7	12:118038289	CGCTGGAGACTCACC[A/G]ACTTCTCTCCAGCTG	55884
rs773205611	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118050831	CCAAGGCAGGTGGAT[C/G]ACCTGAGGTCAGGAG	55884
rs773346443	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118055386	TGAGAAACCCAGATG[C/T]AGTCAAGTATTAAAT	55884
rs773358250	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118045142	AGCACTTTGGGAGGC[C/T]AAGGTGGGCAGATCA	55884
rs773504825	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118048350	CCCAGCACTTTGGGA[G/T]GCCAAGGCAGGTAGA	55884
rs773652008	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033445	GCTAATAAATGGCCA[C/T]TGATAACTCAGTAGC	55884
rs773669341	snp	C/T	1.64768e-05	0.00287021	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042937	TCAGATCTCTCACGA[C/T]ATCTTGGTGGCCGGA	55884
rs773765973	snp	A/G			synonymous-codon	WSB2	GRCh38.p7	12:118035234	ATCTGCCACCGTGGC[A/G]AGGTACAAGCCTTCT	55884
rs773986149	snp	C/T			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033805	CTAGGCAGAAGCCAT[C/T]GTTCCCAGCGGAGGG	55884
rs773991056	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118052088	GTGGTATATAAATTA[C/T]ATCTCAATAAAGCTA	55884
rs774152243	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118057391	GTGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	55884
rs774174892	in-del	-/AA			intron-variant	WSB2	GRCh38.p7	12:118046467	GCAAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA	55884
rs774187397	in-del	-/AAAC			intron-variant	WSB2	GRCh38.p7	12:118057169	CAGAACTTAAAAACA[-/AAAC]AAACAAACAAAAACA	55884
rs774293317	snp	A/G	4.94271e-05	0.00497102	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042885	GTCTTATCCCGTGAC[A/G]CGGAGACCAAAATCA	55884
rs774346540	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040520	AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGC	55884
rs774460363	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118056962	ATGCCAAACATTTCA[C/T]ATGAAATGCTTCTTA	55884
rs774489730	snp	A/G	1.6473e-05	0.00286988	missense	WSB2	GRCh38.p7	12:118034237	CTTTCATTTTCTTGG[A/G]GATTGGCAGTGCTAG	55884
rs774503067	snp	C/T	1.64901e-05	0.00287137	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052442	TCAAACTGGTGGGGG[C/T]GCCCGGGCTTGAGTT	55884
rs774629883	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038047	AGCAATTGTTTTCCC[A/G]TTTTATAAAGGGAAA	55884
rs774705379	snp	C/T	0.000115887	0.00761119	missense	WSB2	GRCh38.p7	12:118036347	CCTTACTGGAGTGAC[C/T]TCAGCCTTTCGCCGG	55884
rs774740138	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118036838	GCCAATAGGGTAGTC[A/G]TATGTGCTGATGAAG	55884
rs774792520	snp	C/T	3.29652e-05	0.00405974	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043222	ACTTGGGGGTGGTGG[C/T]GTGCCCAGAGCTTCC	55884
rs774794578	snp	C/G	1.66349e-05	0.00288395	intron-variant	WSB2	GRCh38.p7	12:118034403	CAGAGCTTGGATGTT[C/G]ATGTTTTCATGAGGA	55884
rs774804277	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050550	AGGCTAGGGCAGGAG[A/G]ATAGCTTGAGACCAG	55884
rs774865158	snp	A/G			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032730	TTAAATAAAGATTGG[A/G]TCTTATCTCACTCTG	55884
rs774880686	snp	A/G	3.30589e-05	0.00406551	intron-variant	WSB2	GRCh38.p7	12:118043018	CAGAGAGGGGGCACG[A/G]GGTGTGCCTGCCACG	55884
rs774951819	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118048636	AACTTCTCACTTAAC[A/G]TATGAAACAATAACA	55884
rs775233620	snp	C/G	1.64732e-05	0.0028699	missense	WSB2	GRCh38.p7	12:118034252	GGATTGGCAGTGCTA[C/G]GACTTGGTAAGTTGT	55884
rs775234680	snp	C/T			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063544	GCAAGTTCGTTTTTC[C/T]AAGTCTTTCAATTTA	55884
rs775359005	snp	A/C/G	9.90568e-05	0.00703706	synonymous-codon	WSB2	GRCh38.p7	12:118036358	TGACCTCAGCCTTTC[A/C/G]CCGGTGTAGGGGTCC	55884
rs775361203	snp	C/T	1.68823e-05	0.00290532	intron-variant	WSB2	GRCh38.p7	12:118052528	CCCCTTGCTCCCTGA[C/T]CACCCAGACACAGGA	55884
rs775412924	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118043070	GAGTGGGGCAGGGAG[A/G]CGACATAGTCAGAAC	55884
rs775428123	snp	A/G	1.65504e-05	0.00287662	intron-variant	WSB2	GRCh38.p7	12:118034389	AACCGATGCTAAGAC[A/G]GAGCTTGGATGTTCA	55884
rs775451028	snp	C/T	1.64914e-05	0.00287149	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052446	ACTGGTGGGGGCGCC[C/T]GGGCTTGAGTTCGGC	55884
rs775589338	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118044403	GAGTTCCCTTATCAC[C/T]AGCTTAGAAATCCCC	55884
rs775600922	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118045895	ACCATTCTACTCTCT[C/G]TTTCTATGAGTTAGA	55884
rs775928558	snp	A/G	1.64765e-05	0.00287019	synonymous-codon	WSB2	GRCh38.p7	12:118035048	ATTGGTCATAGGAGC[A/G]AATGCAATGGGAGTT	55884
rs775973338	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118050746	ACGTATACAAAGGAC[C/G]AGTAAGCACCTGAAA	55884
rs776059314	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118039737	CAAAAATTAATATTT[A/C]TTTTTTATTTTTTTT	55884
rs776127878	snp	A/G	1.65231e-05	0.00287424	intron-variant	WSB2	GRCh38.p7	12:118043011	AGTCAGCCAGAGAGG[A/G]GGCACGAGGTGTGCC	55884
rs776173513	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038197	TATTGGGGTGGATTT[A/G]CGGACGATTTTGAGA	55884
rs776322376	snp	G/T	4.94368e-05	0.00497152	missense	WSB2	GRCh38.p7	12:118035019	CCATGTGGAAAAAAT[G/T]TGCAGCAAAGCCCAT	55884
rs776519153	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040191	AAATAAAGGTCAATC[A/G]TGGTTTCTTCAGCTG	55884
rs776558602	snp	A/G			synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043290	CCAGACAATCTGACC[A/G]CAGTCCAGCGTCTTC	55884
rs776589314	snp	C/G	1.64974e-05	0.00287201	missense	WSB2	GRCh38.p7	12:118036456	AGACAACACTGCTTT[C/G]ATGGCCCTCTAGCTT	55884
rs776870457	snp	A/G	3.29843e-05	0.00406092	intron-variant	WSB2	GRCh38.p7	12:118035200	GGCCATGTAAAGAGA[A/G]TTCTCTTCGTTACCT	55884
rs776923515	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118060014	CAAGATTACCATGAA[A/G]TTCTGGAACAAATTC	55884
rs776950499	snp	A/G	0.000120987	0.00777681	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043335	CCGCCCTTTCGTCTC[A/G]TTTTTGCTACTTCGG	55884
rs777144848	snp	C/T	3.37804e-05	0.00410963	intron-variant	WSB2	GRCh38.p7	12:118052280	TGTTTGGAAATGCGC[C/T]GGATGGGGCCCCAGT	55884
rs777270301	snp	C/T	1.70557e-05	0.0029202	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043321	TCTTTTGGGCTGCCC[C/T]GCCCTTTCGTCTCAT	55884
rs777378332	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118053176	AAGCTCCCGCCTGCC[G/T]ACATCATAAAGGCAA	55884
rs777391097	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118036197	ACAGAGCGAGACTCC[A/G]TCTCAAAAGAGACCC	55884
rs777464085	snp	A/G	1.66043e-05	0.00288129	intron-variant	WSB2	GRCh38.p7	12:118035140	GCTGACCCAGGGCCA[A/G]ACCAAGAGGGCCTTG	55884
rs777478043	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118041864	GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC	55884
rs777544682	snp	A/G	0.00010858	0.00736736	intron-variant	WSB2	GRCh38.p7	12:118043411	TCTTAATGAATCTGC[A/G]ATTGTTACCAGTCTA	55884
rs777660616	snp	C/T	1.64776e-05	0.00287028	missense	WSB2	GRCh38.p7	12:118034347	CAGAACTGGACGTGG[C/T]CATCTCTTGTCCTAA	55884
rs777666769	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118050213	AGAAACTACGCAACC[A/G]AGGCTGGCTGAATGA	55884
rs777747241	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042878	GCGAAGAGTCTTATC[C/T]CGTGACGCGGAGACC	55884
rs777750703	snp	C/T	3.3006e-05	0.00406226	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042971	ATTCAAAAGCAGGAG[C/T]CCTGGCATGGGAGCA	55884
rs777758763	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118038638	GCTTCAACACAATCT[A/G]TAAGATCAGTAAGGG	55884
rs777773963	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118059254	TTGATTACATGTAGC[A/C]GGAATATTTTAGACA	55884
rs777807817	snp	A/G	0.000115372	0.00759424	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052399	TGGGGAGAAGGCGAC[A/G]CTCCAGGTTTCACAG	55884
rs777967794	snp	C/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118063028	TTGTCCAGGCTCCCC[C/T]CTCCCATTTTTCTCT	55884
rs778170328	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063930	CACAGAATTGTGGAG[A/G]CCCCCTTCCCAGGCT	55884
rs778171538	in-del	-/AGG	1.65343e-05	0.00287521	intron-variant	WSB2	GRCh38.p7	12:118052486	CGGTTCCTCTGGGGC[-/AGG]AGACAACATGCTTCA	55884
rs778205866	snp	A/G	6.62844e-05	0.00575655	intron-variant	WSB2	GRCh38.p7	12:118052496	GGGGCAGGAGACAAC[A/G]TGCTTCAAACACACA	55884
rs778289414	snp	C/T	6.59196e-05	0.00574068	missense	WSB2	GRCh38.p7	12:118035293	TAATGTGGACGTCAC[C/T]GTCATCCATGGCGGG	55884
rs778396707	snp	A/G	0.000119152	0.00771763	intron-variant	WSB2	GRCh38.p7	12:118036527	TGTGGAAAGTAAGAA[A/G]TGCCTGGTTAGGGCA	55884
rs778421139	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118042660	AAACTCTATTTGGTA[C/T]AGTATTATCTTTGGG	55884
rs778484500	snp	A/G/T	9.88572e-05	0.00702993	stop-gained, synonymous-codon	WSB2	GRCh38.p7	12:118036394	AATCACATTGGTATC[A/G/T]TAAGAAGCCGTGACA	55884
rs778487854	snp	G/T	1.64961e-05	0.00287189	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052333	CTCCAACGGCCAGGG[G/T]ATCAGTTTGACGATG	55884
rs778613501	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118043822	TTTTTGTTTCTTTTT[A/C]AGAGTTGATGTAGGC	55884
rs778620944	snp	C/G			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062589	TTCTACGGTAACTGA[C/G]GTTCCCGTGTTCTTT	55884
rs778720443	snp	A/C					GRCh38.p7	12:118034825	AGAGAAAATGGGACA[A/C]CGTTATTAGCAAAAT	55884
rs778857440	in-del	-/A			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063979	AACAAGAAAAAAGTC[-/A]GTTGCAATGGACCTG	55884
rs778913192	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118048037	GTGCAGGTGATCCTC[C/G]CATCTCAGCCTCCTG	55884
rs778918891	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118058310	TCTCAGAGACCATCC[C/T]GGCCTCACTATCTAA	55884
rs778969119	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043167	CTTGATCTGCCCATC[A/G]TTGAGTCCCGTAGCA	55884
rs778982084	snp	C/T	1.6477e-05	0.00287024	missense	WSB2	GRCh38.p7	12:118036423	CAAGCAGGGCAGAGT[C/T]GGGGGAGAAGTCACA	55884
rs779052904	snp	A/G	1.65091e-05	0.00287303	intron-variant	WSB2	GRCh38.p7	12:118042982	GGAGCCCTGGCATGG[A/G]AGCAGGGGCACTGAG	55884
rs779163340	snp	C/G	1.65633e-05	0.00287774	intron-variant	WSB2	GRCh38.p7	12:118034963	GAAAGCACCACCCAT[C/G]TGTTCAGCTAACAAA	55884
rs779194145	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118039310	AAAATAAAAAAGCCC[A/G]TCCATATAGAGGATG	55884
rs779209168	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118049363	ATGCAACTAATTTCA[C/T]GATGAAGATCAGTGT	55884
rs779302949	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118050477	AAGACCCTGTCTCTA[C/T]AAAAAATTTAAAAGT	55884
rs779367800	snp	A/C/G	3.48324e-05	0.00417316	intron-variant	WSB2	GRCh38.p7	12:118036553	GGGCAGAAGCAAAGT[A/C/G]CTTAGGACTCAAACG	55884
rs779409537	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118064012	GTGTGTATCTTCCTG[A/G]TCCTGATAAATAGAT	55884
rs779421796	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118053666	TAGTTCAGTTCTCTA[C/T]TCTGATGGAAGATTC	55884
rs779507167	in-del	-/C			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033628	TGTAATTTAGTTAAG[-/C]TAAATTAATACCTCA	55884
rs779543876	snp	A/C/G	0.000752498	0.0193846	synonymous-codon, upstream-variant-2KB, intron-variant	WSB2	GRCh38.p7	12:118062115	TACGGCGACAGCCTC[A/C/G]CCTGTCCCCGTCCCC	55884
rs779578715	in-del	-/A			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063437	GGCTCCGTCTGGAGG[-/A]AAAAAAAAAAAAAAA	55884
rs779651889	snp	G/T			downstream-variant-500B, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032646	ACATCCTCAGCCCCC[G/T]GAGTAGCTGGGGCTA	55884
rs779706909	snp	C/T	1.6517e-05	0.00287372	intron-variant	WSB2	GRCh38.p7	12:118042994	TGGGAGCAGGGGCAC[C/T]GAGTCAGCCAGAGAG	55884
rs779713610	snp	C/T	4.94222e-05	0.00497078	synonymous-codon, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043176	CCCATCGTTGAGTCC[C/T]GTAGCAAGAACCAGG	55884
rs779739161	snp	C/T	3.29582e-05	0.00405931	missense	WSB2	GRCh38.p7	12:118036386	TCCCACATAATCACA[C/T]TGGTATCGTAAGAAG	55884
rs779789609	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118054929	CACGCCTATAATCCT[A/G]GCACTTTGGTAGGCC	55884
rs780053034	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118047137	AAAGAATTAAGGCAT[A/G]TTTATTATTTCATTT	55884
rs780105270	snp	G/T	1.6522e-05	0.00287414	intron-variant	WSB2	GRCh38.p7	12:118035100	CTGAGGAGTCTGGAT[G/T]GGGAGAGAGAACATC	55884
rs780222378	snp	A/G	3.29549e-05	0.00405911	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034189	GAAGCACAAGATGTG[A/G]TGTTGCTTAAAAAGT	55884
rs780226068	snp	C/T	1.66913e-05	0.00288883	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118038386	ACACTTGAATCTGTT[C/T]ACCTGGCAGGAAAAA	55884
rs780236887	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118051529	AAAGGCTACGTGTTG[C/T]ATGACTCCATTAATA	55884
rs780247765	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118041216	ATGGTATTAGGAGGC[A/G]GGGCTTTTGAGAAGT	55884
rs780319748	snp	C/G	4.16198e-05	0.0045616	intron-variant	WSB2	GRCh38.p7	12:118038245	GCCACCACTTCAGAC[C/G]TCCATGTCTCAGTGA	55884
rs780406245	snp	A/G	1.70153e-05	0.00291674	intron-variant	WSB2	GRCh38.p7	12:118052270	GAACAAGGAGTGTTT[A/G]GAAATGCGCCGGATG	55884
rs780443406	in-del	-/G			intron-variant	WSB2	GRCh38.p7	12:118054439	ACTTTGTGAGGCCAA[-/G]GCGGGCAGATCACCT	55884
rs780446055	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118040268	GGTCAGTGGGGCAGC[A/G]CCTGTCAGCTGGGAA	55884
rs780697348	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	WSB2	GRCh38.p7	12:118034313	GTGCTTCAGTGAGGA[C/T]AGGACCCTAGGAGCT	55884
rs780707023	snp	A/G			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033264	AGTTAAACAGCAGAG[A/G]CAGATCTCGTACATA	55884
rs780802086	snp	C/G	1.68858e-05	0.00290561	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118043313	GCGTCTTCTCTTTTG[C/G]GCTGCCCCGCCCTTT	55884
rs780811619	snp	A/C			intron-variant	WSB2	GRCh38.p7	12:118051739	AGCACTTCGGGAGGC[A/C]GAGGTGGGTGAATCA	55884
rs780822193	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118046584	CCATGAATGTCACTT[C/T]GATCGGCTGCCTCTC	55884
rs780884523	snp	C/T	1.65501e-05	0.00287659	intron-variant	WSB2	GRCh38.p7	12:118035115	GGGGAGAGAGAACAT[C/T]TGGATATTAGCTGAC	55884
rs781016549	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118045105	TAACTGGCCGGGTGC[A/G]GTGGCTCATGCTTGT	55884
rs781070269	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118048689	TAAATATGAAAAAAA[-/A]TGGTTAATACTCAAA	55884
rs781118957	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118056666	AACACTTTGGGAGGC[C/T]GAGGCAGGCAGGTCA	55884
rs781200933	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118047899	AAAACAAATCTGATA[C/T]CATACTGCATACATG	55884
rs781296637	in-del	-/TTT			intron-variant	WSB2	GRCh38.p7	12:118041749	CCTCTCTTATGTCAC[-/TTT]TTTTTTTTTTTTTTT	55884
rs781325042	snp	A/G	3.29663e-05	0.00405981	missense, intron-variant, utr-variant-5-prime	WSB2	GRCh38.p7	12:118042865	TCAGGTCCCAGATGC[A/G]AAGAGTCTTATCCCG	55884
rs781332487	snp	A/G	1.70921e-05	0.00292331	intron-variant	WSB2	GRCh38.p7	12:118038415	AAGAAGCAAACAATG[A/G]GCCAGTCCTCAACAA	55884
rs781357348	snp	A/G	1.64762e-05	0.00287016	utr-variant-3-prime	WSB2	GRCh38.p7	12:118034194	ACAAGATGTGGTGTT[A/G]CTTAAAAAGTCCTGT	55884
rs781359782	snp	C/T			intron-variant	WSB2	GRCh38.p7	12:118041537	ATGGCTGTGTGGAGC[C/T]GGACAGTCATAGCTT	55884
rs781376897	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118048203	CAATGTGCTGGGATT[A/T]CAGGCGTGAGCCACC	55884
rs781441613	snp	A/C/T	8.24268e-05	0.00641933	missense	WSB2	GRCh38.p7	12:118035305	CACTGTCATCCATGG[A/C/T]GGGGTCAACCTGGGT	55884
rs781468523	snp	C/G			intron-variant	WSB2	GRCh38.p7	12:118049024	ATACAAATTTGAAAA[C/G]AAGAGTGATTTTCAG	55884
rs781468673	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118036639	CTCTATCCCTTTTCT[A/G]CAGCTCTTCCAGAAC	55884
rs781489730	snp	A/G			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062584	ATGTTTTCTACGGTA[A/G]CTGAGGTTCCCGTGT	55884
rs781494935	in-del	-/A			upstream-variant-2KB, downstream-variant-500B	WSB2, VSIG10	GRCh38.p7	12:118063439	CTCCGTCTGGAGGAA[-/A]AAAAAAAAAAAAAAA	55884
rs781738117	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118040654	AGGAGGCTCTGTCTC[-/A]AAAAAAAAAAAAAAA	55884
rs781747420	snp	C/T			downstream-variant-500B, utr-variant-3-prime, intron-variant	RFC5, WSB2	GRCh38.p7	12:118032438	GTTGGCCAATCCATT[C/T]CCAGCTCTTCTGCTG	55884
rs781758176	snp	A/C	1.68241e-05	0.00290031	intron-variant	WSB2	GRCh38.p7	12:118036315	CCCCCACAAAAAAGT[A/C]ATAGCAGGGATTCAG	55884
rs781758614	snp	A/G	1.65083e-05	0.00287296	missense, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052472	TCGGCCAGCAGCAGC[A/G]GTTCCTCTGGGGCAG	55884
rs781781296	snp	A/G	1.64817e-05	0.00287064	synonymous-codon, utr-variant-5-prime	WSB2	GRCh38.p7	12:118052378	CCAAGCAAACCAGGA[A/G]CCATCTGGGGAGAAG	55884
rs796133340	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118046483	AAAAAAAAAAAAAAA[-/A]GAAAGAAAAAATTTG	55884
rs796232418	in-del	-/AA			intron-variant	WSB2	GRCh38.p7	12:118045715	GACACTGTCTCAAAG[-/AA]AAAAAAAAAAAAAAG	55884
rs796292236	in-del	-/A			intron-variant	WSB2	GRCh38.p7	12:118050190	ACTCCATCTCAAAAG[-/A]AAAAAAAAGAAACTA	55884
rs796404612	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118047882	TACACAAATGTCTTT[A/T]AAAAACAAATCTGAT	55884
rs796442403	snp	G/T			intron-variant	WSB2	GRCh38.p7	12:118035800	AAATAAAGAGTCATA[G/T]TGAGGCTTCATAATG	55884
rs796549670	snp	A/G			intron-variant	WSB2	GRCh38.p7	12:118034804	TTACATTTAGGTTAA[A/G]TATTCAGAGAAAATG	55884
rs796773753	in-del	-/A			utr-variant-3-prime, downstream-variant-500B	WSB2, RFC5	GRCh38.p7	12:118033547	ATGCACACCATTGTT[-/A]AAAAAAAAAAAAAAA	55884
rs796784032	snp	A/T			intron-variant	WSB2	GRCh38.p7	12:118054690	CTCAAAAAATAATAA[A/T]AATAATAATAATAAT	55884
rs796889449	in-del	-/T			upstream-variant-2KB	WSB2	GRCh38.p7	12:118062747	GCCGGTTTTTTTTTT[-/T]CTTTTCTTTGAACCT	55884
rs796906231	snp	G/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	WSB2, VSIG10	GRCh38.p7	12:118063953	CCCAGGCTCCACCAG[G/T]GTTTGAGAAAAACAA	55884

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