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

CDC20B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs173041	snp	A/G			intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172838	TACGACCAGGGCTTA[A/G]AGTTTCGTACCACCT	166979
rs173042	snp	G/T	0	0	missense, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172979	CCCTCCGAGGCGCGG[G/T]GCGCTCCAGTTTCCA	166979
rs182858	snp	A/G	0.490007	0.0699769	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137248	TAATTGCCTGTGGCA[A/G]TTTCTAGAAGGTCCT	166979
rs186762	snp	A/G	0	0	intron-variant	CDC20B	GRCh38.p7	5:55135248	tctttctctctctGT[A/G]TATATATATATATAG	166979
rs191396	snp	G/T	0.289039	0.246933	intron-variant	CDC20B	GRCh38.p7	5:55143685	TCAAAGTGATTATCT[G/T]GTTTTAAAAACCAAA	166979
rs193104	snp	G/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55131457	ttttttgctgatttg[G/T]gtttctcttccattt	166979
rs193105	snp	C/T	0.299916	0.244966	intron-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170174	GACTTCACTGAAAAT[C/T]TGGGGACACATTGTA	166979
rs233625	snp	A/G	0.48178	0.0936921	intron-variant	CDC20B	GRCh38.p7	5:55157548	TTTGAAAACTTACGT[A/G]TATATCTCCTGTCAA	166979
rs336061	snp	A/G	0	0	intron-variant	CDC20B	GRCh38.p7	5:55120340	AGAGAAAGAGAGCTT[A/G]TTGGGGGCATAGGCT	166979
rs336062	snp	C/T	0.282105	0.24793	intron-variant	CDC20B	GRCh38.p7	5:55121058	GTTCAGAAAATAAAA[C/T]TGCCTTCTATTTATT	166979
rs336071	snp	A/T	0.261608	0.24973	intron-variant	CDC20B	GRCh38.p7	5:55146202	ctgaagctcagcttc[A/T]gtgattggcggagac	166979
rs336072	snp	A/G	0.26078	0.249767	intron-variant	CDC20B	GRCh38.p7	5:55145737	agaggaggaggagga[A/G]gaagaAAGAAGAAAG	166979
rs336073	snp	C/T	0.480931	0.0957637	intron-variant	CDC20B	GRCh38.p7	5:55144757	TGTATATAACTGTGA[C/T]GATTGTCAGTACTAG	166979
rs336074	snp	G/T	0.280328	0.248154	intron-variant	CDC20B	GRCh38.p7	5:55144191	TTCTGCAATAGAAAG[G/T]GGGAGAGAGGCAAAG	166979
rs336075	snp	A/G	0.26078	0.249767	intron-variant	CDC20B	GRCh38.p7	5:55144122	CAAAGCAAGCATCCC[A/G]TAATGTTTTCCTTGC	166979
rs336076	snp	A/G	0.481087	0.0953875	intron-variant	CDC20B	GRCh38.p7	5:55144064	CCATAGTTTTAAATG[A/G]TAGTGGAAAGAGTAT	166979
rs336077	snp	C/T	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55141562	tgtttacattcttcg[C/T]gactcagtgagtata	166979
rs336078	snp	A/G	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55141069	aacatGACCTTTGGC[A/G]TAGTTCTGAACCTGA	166979
rs336079	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55138225	TGTAGTGAGCCGAAA[C/T]CACGCCACTGCACTC	166979
rs336080	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55137776	CTATATTCACTCCCA[C/T]AGTGTTTGTTCTTGT	166979
rs336081	snp	C/T	0.488184	0.0759499	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137565	GACTAATTGAGAGGC[C/T]CTCTGAATACTCTAT	166979
rs336082	snp	A/G	0.299664	0.245017	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159611	GGCAATCAAATACCA[A/G]GTGAATACAGTCAAA	166979
rs336083	snp	A/T	0.481473	0.0944461	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159189	GTCTCTAAAAAAGAA[A/T]TTTAATTAGCTGGTT	166979
rs336084	snp	A/T	0.299916	0.244966	intron-variant	CDC20B	GRCh38.p7	5:55156954	ATATGAGAACACACA[A/T]GAAACGGAAGGATTA	166979
rs336085	snp	A/G	0.471673	0.115589	intron-variant	CDC20B	GRCh38.p7	5:55156046	GCCATGTGGAACTGT[A/G]AGTCCATTAAATCTC	166979
rs336086	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55154852	actaacaaatgagta[A/T]ttaaatacaatttat	166979
rs336087	snp	A/G	0.471004	0.116864	intron-variant	CDC20B	GRCh38.p7	5:55154174	ccttggatgtgctgg[A/G]gtgttgtcccattac	166979
rs336088	snp	C/T	0.278133	0.248412	intron-variant	CDC20B	GRCh38.p7	5:55152425	aataaacactccctc[C/T]gattcatatatccca	166979
rs336089	snp	C/T	0.330249	0.23677	intron-variant	CDC20B	GRCh38.p7	5:55149445	tgatgagtgtttggg[C/T]tgtctgcaccttctt	166979
rs336090	snp	C/T	0.262159	0.249704	intron-variant	CDC20B	GRCh38.p7	5:55148673	tctcactttgtcgcc[C/T]aggctggagtgcagc	166979
rs336099	snp	C/G	0.325799	0.238232	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55135984	tgctctctagcttgg[C/G]tgacagagtgagact	166979
rs336100	snp	C/T	0.326035	0.238157	intron-variant	CDC20B	GRCh38.p7	5:55135012	cattagagttcattc[C/T]tgatgttatgtattc	166979
rs336101	snp	A/G	0.33875	0.233717	intron-variant	CDC20B	GRCh38.p7	5:55134373	GCAGTTTTGCCCTCA[A/G]CTACAGGTTTTCATA	166979
rs336102	snp	A/G	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55134146	GTTTGAACTTAGTAT[A/G]GTCTTTTGATGAGAA	166979
rs336103	snp	A/G	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55131360	GTTCTATTTTAATTG[A/G]TCTTAGCTTTTTGGC	166979
rs336104	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55131327	TATCTCTTTGTATTG[G/T]GTTTTGTCGTCATTT	166979
rs336105	snp	A/G	0.490007	0.0699769	intron-variant	CDC20B	GRCh38.p7	5:55130447	gagaaCCCCATGGTC[A/G]CCTTGTTATCCTGCT	166979
rs336106	snp	A/G	0.489434	0.0719116	intron-variant	CDC20B	GRCh38.p7	5:55130420	TGCTTCTAAGACCTG[A/G]CTCTACTTACACATA	166979
rs336114	snp	C/T	0.277867	0.248442	intron-variant	CDC20B	GRCh38.p7	5:55167894	Taaattagccaggtg[C/T]ggtagcacacacctg	166979
rs336115	snp	C/T	0.446902	0.154045	utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173093	GTCTTGACGCCTAAT[C/T]GTCAAACCCCTGGAG	166979
rs336116	snp	A/G	0.438386	0.164349	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55174247	TTTTTTTTTTTTTTG[A/G]ATCACTGACCCTTTT	166979
rs368003	snp	A/G	0	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172794	AACTAGGCACCTTCA[A/G]AATATAACTAAATTA	166979
rs369527	snp	A/G			upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159266	actttgggaggccta[A/G]atgggaggatcactt	166979
rs381852	snp	C/T	0.308378	0.243088	missense, intron-variant, utr-variant-3-prime, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164133	ATGGGCTCCTCTGGC[C/T]TCCAGAACTTCACAA	166979
rs382402	snp	G/T	0.322607	0.239224	synonymous-codon	CDC20B	GRCh38.p7	5:55124971	AGCCCAGCATCATGT[G/T]GGAACACTTCGCCAC	166979
rs384818	snp	C/T	0.289683	0.24683	intron-variant	CDC20B	GRCh38.p7	5:55115997	AGGGGCCTGCATTGT[C/T]GTTATAAATGTAAAC	166979
rs389075	snp	C/T	0.336017	0.234736	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113759	CTTGAAAAACACTTA[C/T]TAAAATCTCACTATA	166979
rs390074	snp	G/T			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137205	ATTTGGAGCTCTCAG[G/T]GCtttctttcttttt	166979
rs391112	snp	G/T	0.281841	0.247964	intron-variant	CDC20B	GRCh38.p7	5:55117261	GTCATGATTTTTTTT[G/T]GGGGGAAAATTTCAG	166979
rs396335	snp	C/T	0.0711525	0.174681	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112678	TAATTTGTCAATATA[C/T]ATTTTTATTTTTCCT	166979
rs402018	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55153165	tggaacctttgcctt[C/T]tgggcttaagccatc	166979
rs403881	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55153236	atagccagaccttgt[C/T]tcataaaaaaaaaaa	166979
rs409095	snp	A/G	0.390651	0.206682	intron-variant	CDC20B	GRCh38.p7	5:55139704	CATCAGTTTCTCGAC[A/G]TGCTTATATCACACT	166979
rs417992	snp	C/T	0.323197	0.239044	intron-variant	CDC20B	GRCh38.p7	5:55139707	GTGATATAAGCATGT[C/T]GAGAAACTGATGAAA	166979
rs423074	snp	C/T	0	0	missense, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172952	CCCACAGCATCTCCT[C/T]TTCCGTGCGGACCCT	166979
rs423451	snp	A/G	0	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162322	aatcgcttgaaccca[A/G]aggcagaggttgcag	166979
rs424203	snp	A/G	0.376195	0.215812	intron-variant	CDC20B	GRCh38.p7	5:55116469	ATTTATTTATTTTGA[A/G]ACAGGGTCTCACTCT	166979
rs426722	snp	G/T	0	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162126	aaaggccgggcgcgg[G/T]ggctcacgcctgtaa	166979
rs433328	snp	A/T	0.34303	0.232046	intron-variant	CDC20B	GRCh38.p7	5:55123737	AAACAAAACAAAAAA[A/T]TAGTTGAAAACCCAA	166979
rs434658	snp	A/G	0.481932	0.0933148	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163076	tttgaagcacggagc[A/G]tacattaatctggca	166979
rs436282	snp	C/T	0.481932	0.0933148	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162935	aggcccgtatatcaa[C/T]cctggctcaaccact	166979
rs444527	snp	C/T	0.321308	0.239615	missense	CDC20B	GRCh38.p7	5:55114271	AGTCCAGACCAGACC[C/T]GGGTGTTTTCTGCTG	166979
rs903887	snp	C/T	0.282632	0.247861	intron-variant	CDC20B	GRCh38.p7	5:55125463	TTAGATATTTATTTC[C/T]TTTTTCTATGTCTAA	166979
rs903888	snp	C/G	0.297382	0.245469	intron-variant	CDC20B	GRCh38.p7	5:55125344	CCTGTATATAAACTA[C/G]TCTTTGGGAAAATCT	166979
rs963748	snp	C/T	0.367708	0.220556	intron-variant	CDC20B	GRCh38.p7	5:55146134	TGAGTCCCTACATCT[C/T]AAACTGCAACCTAAC	166979
rs1021580	snp	C/T	0.305591	0.243741	missense	CDC20B	GRCh38.p7	5:55143638	TTTCTTGTAGGATCC[C/T]GCAAAGAACAACTGA	166979
rs1047689	snp	A/G	0.000155552	0.0088177	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164231	TGAGAATGCCATTGC[A/G]TTTCTAATAGAACAG	166979
rs1335673	snp	A/G	0.315273	0.241329	intron-variant	CDC20B	GRCh38.p7	5:55150222	TTTAAAAATGGTAAC[A/G]TAGGATAATAGTGAA	166979
rs1393163	snp	A/C	0	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136777	TTGGGAGCCAGAATT[A/C]TGTGTGAGAATCCTC	166979
rs1414365	snp	G/T	0.0558544	0.157504	intron-variant	CDC20B	GRCh38.p7	5:55126642	TTAAAAAGAAGCAGT[G/T]AAACTAAATCACTAG	166979
rs1414366	snp	C/T	0.0372196	0.131242	intron-variant	CDC20B	GRCh38.p7	5:55126885	TGAATTGGAAATGTG[C/T]CCCAGAGAGCTTAAC	166979
rs1501829	snp	C/T	0.0103295	0.0711199	intron-variant	CDC20B	GRCh38.p7	5:55146296	taggaattggaagtg[C/T]gtaggagccggcctg	166979
rs1692473	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55126427	taggctggagttcag[G/T]ggcgtgatctcagct	166979
rs1692474	snp	C/T	0.332337	0.236052	intron-variant	CDC20B	GRCh38.p7	5:55126185	ATGTATTTAAGTAAT[C/T]TGATGTAAACTTGAG	166979
rs1697945	snp	A/C	0.297382	0.245469	intron-variant	CDC20B	GRCh38.p7	5:55125597	AGACATTATCCACTG[A/C]TTAGGAATCATATTG	166979
rs2062703	snp	C/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55142529	TAAGACTTCCTTTTC[C/T]TTCCTCTTATCCTTT	166979
rs2270910	snp	C/G	0.234401	0.249513	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160906	ATCCTAAACAATTTG[C/G]GGGGGACTATAACCT	166979
rs2407932	snp	A/G	0.300673	0.244811	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164768	AATCCTTATATATGT[A/G]TGCTTGTTTTGTGTA	166979
rs2645032	snp	C/T	0.0197687	0.0974348	intron-variant	CDC20B	GRCh38.p7	5:55122078	CTTAATTAGTGGGAG[C/T]AGAAGTGTGGAGCAT	166979
rs2783480	snp	C/T	0.0368353	0.130617	intron-variant	CDC20B	GRCh38.p7	5:55132886	CTTTCCAAGTTCTAA[C/T]GATCTTCCAAGACCC	166979
rs2783487	snp	C/T	0.490007	0.0699769	intron-variant	CDC20B	GRCh38.p7	5:55121565	TGCTCTCATAAAGTA[C/T]ATTGTAATGAATACA	166979
rs2935260	snp	A/T	0.363776	0.222609	intron-variant	CDC20B	GRCh38.p7	5:55149052	TCTCCACTGGTAAAC[A/T]CTTAGTCTCTGTCTC	166979
rs2937583	snp	C/T	0.366885	0.220993	intron-variant	CDC20B	GRCh38.p7	5:55148793	aaaaccctgtacata[C/T]ggtttcatacatagt	166979
rs2937584	snp	A/G	0.0414363	0.137845	intron-variant	CDC20B	GRCh38.p7	5:55142898	TTTGAAGGAATCCAT[A/G]TTTCAGTTCGAAAGC	166979
rs2937585	snp	A/G	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55121402	TAATCAGGATATAAC[A/G]ACACGATGGAATATT	166979
rs2992406	snp	A/G	0.363359	0.222822	intron-variant	CDC20B	GRCh38.p7	5:55149155	ggaaatgtaaactaa[A/G]ccacaccaaagcacc	166979
rs3068520	in-del	-/A	0	0	intron-variant	CDC20B	GRCh38.p7	5:55144011	AAAAAAAAAAAAAAA[-/A]CCAGATTTGCACATT	166979
rs3104230	snp	G/T	0.0325213	0.123301	missense	CDC20B	GRCh38.p7	5:55114292	AGAGTGCTGCACCTG[G/T]CTTTGAGTCCAGACC	166979
rs3104237	snp	A/G	0.380138	0.213458	intron-variant	CDC20B	GRCh38.p7	5:55145323	TCTGCAGATTGAAAG[A/G]GAGCCCAGATTTTTT	166979
rs3105152	snp	C/G	0.0387552	0.1337	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136426	GATTACAGGCCTGTG[C/G]TACCACACCTGGCCA	166979
rs3105153	snp	A/G	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55115410	TGAGAAGTACTGCCT[A/G]TTGTTGCCTCATCTC	166979
rs3111178	snp	C/T	0.0414363	0.137845	intron-variant	CDC20B	GRCh38.p7	5:55152436	aatcggagggagtgt[C/T]tattttagtttcatc	166979
rs3111179	snp	C/T	0.467946	0.122472	intron-variant	CDC20B	GRCh38.p7	5:55153129	CTATAGTCCCAGCTG[C/T]TCAGGAGACTGAGGT	166979
rs3111197	snp	C/G	0.0372196	0.131242	intron-variant	CDC20B	GRCh38.p7	5:55132159	ACATTTTTTGAAAAT[C/G]CATCCTTCTTAGTTG	166979
rs3111198	snp	A/T	0.152778	0.230321	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136576	AAAAAAAAAAAAAAA[A/T]TAGGACAAGCCATAA	166979
rs3111199	snp	C/G	0.0387552	0.1337	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137339	TTTCCTACCAGCTTT[C/G]GGCAAAGAGGTACAC	166979
rs3747725	snp	A/G	0.215144	0.247558	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166162	TGCATTCACGTTAGG[A/G]GCATGAGCAGAACTG	166979
rs4547887	snp	C/T	0.00159617	0.0282053	intron-variant, splice-acceptor-variant	CDC20B	GRCh38.p7	5:55137637	TGCCACTAAAGTGAT[C/T]TATGGGAAGGGGAGA	166979
rs5867963	in-del	-/G			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137493	AATTACTTGGCTTAT[-/G]GTGGGATCTGTTTCA	166979
rs5867965	in-del	-/TCTCTT	0.245916	0.249967	intron-variant	CDC20B	GRCh38.p7	5:55145769	TCTCCTCCTCTCTTC[-/TCTCTT]TCTCTTTGTCTCTCT	166979
rs5867967	in-del	-/A	0.438105	0.164671	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55174311	CATACTGAAAGCAAG[-/A]AAAAAATGGCATTAG	166979
rs5867968	in-del	-/C	0.416545	0.186448	upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174516	CAAATTCCAGTAAAT[-/C]CTTTCAGCAAACATT	166979
rs6450294	snp	A/G	0.303438	0.244222	intron-variant	CDC20B	GRCh38.p7	5:55157819	GGGCCCTGCCTAAGC[A/G]GTGGTCAGTCAACAT	166979
rs6450295	snp	C/T	0.289165	0.246913	intron-variant	CDC20B	GRCh38.p7	5:55168788	GGGTACACATGGACA[C/T]GAAGATGGAAACAGT	166979
rs6450296	snp	A/G	0.0962929	0.197165	intron-variant	CDC20B	GRCh38.p7	5:55168851	aggaatacaaggact[A/G]aaaaactatctattg	166979
rs6866944	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55155605	CCAAAATGTTCATCG[C/T]CTCATGTTTGAACTT	166979
rs6873626	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55149235	gcattggtaaggatg[C/T]gaagaaactggaatc	166979
rs6883587	snp	G/T	0.356597	0.226135	intron-variant	CDC20B	GRCh38.p7	5:55121353	TTCCACGTTTTAATA[G/T]ACTTTTCACAATTAT	166979
rs6887333	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55140072	agtttaccaatatta[C/T]ttagaaaatagatgt	166979
rs6893188	snp	A/T	0.0744748	0.178019	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112542	ATTAGGAAGATCAAA[A/T]TAAAACCATTAAAGA	166979
rs6894721	snp	A/C	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55149357	ccacatgaccaagca[A/C]gtccactcataggta	166979
rs6894744	snp	A/C	0.296873	0.245566	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158173	GTCTGGGGTGGGGCC[A/C]AAAATGCTGTGTTTC	166979
rs7444185	snp	A/G			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137529	TAAGTTCCCTTAAAA[A/G]AATCAACAACAGAGC	166979
rs7702771	snp	A/G	0.0513262	0.151752	intron-variant	CDC20B	GRCh38.p7	5:55119214	CTGGGCTGGGTAGAG[A/G]AGATACTCTACTCAC	166979
rs7710215	snp	A/G	0.079617	0.182947	intron-variant	CDC20B	GRCh38.p7	5:55153610	ataaatccccccggg[A/G]tggactgaaggttta	166979
rs7711346	snp	C/T	0.0209421	0.100162	intron-variant	CDC20B	GRCh38.p7	5:55131125	gtgacagagtgaaaa[C/T]ctccctcaaaacctc	166979
rs7712791	snp	G/T	0.0482946	0.147699	intron-variant, upstream-variant-2KB, downstream-variant-500B	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172067	CTCTTTATGAAACAC[G/T]TTTATAAAACCATTT	166979
rs7713889	snp	C/G	0.29789	0.24537	intron-variant, upstream-variant-2KB, downstream-variant-500B	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172054	AAGCAGATGAAGGCT[C/G]TTTATGAAACACGTT	166979
rs7716364	snp	C/T	0.0460142	0.144533	intron-variant	CDC20B	GRCh38.p7	5:55154498	ctgcagcctgggtga[C/T]agagtgagaccgtgt	166979
rs7720107	snp	C/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55122992	cactaagtttttgag[C/T]aatttgttgcacagc	166979
rs7725958	snp	C/T	0.0441095	0.141807	intron-variant	CDC20B	GRCh38.p7	5:55168968	atgtaccccctggat[C/T]taaaataaaaTAAAG	166979
rs7727157	snp	C/T	0.0566069	0.158427	intron-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170382	GTAATTGTAATACTT[C/T]CCTTACCATTATAAA	166979
rs7729370	snp	A/C	0.0821764	0.185298	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113355	GAGCCAAGGCAAAAA[A/C]AGATCTCCTAACTTC	166979
rs10043273	snp	C/G	0.245061	0.249951	intron-variant	CDC20B	GRCh38.p7	5:55127204	CTGTTTACTCAGGCC[C/G]CATAATCAATTGTTA	166979
rs10043664	snp	A/C	0.244776	0.249945	intron-variant	CDC20B	GRCh38.p7	5:55132482	TCAAGCATAGTCTTT[A/C]CTCTCCAAATCACCT	166979
rs10045164	snp	A/G	0.247905	0.249991	intron-variant	CDC20B	GRCh38.p7	5:55153997	AGTGTCCAGAACAGG[A/G]GCAATCTAAACTCTG	166979
rs10050963	snp	A/G	0.243633	0.249919	intron-variant	CDC20B	GRCh38.p7	5:55147097	ACATAAATATGTTAT[A/G]TTTTATATATTTATA	166979
rs10051621	snp	G/T	0.0659589	0.169201	intron-variant	CDC20B	GRCh38.p7	5:55126805	ttctgatacatgttc[G/T]agtttgagaactact	166979
rs10054014	snp	C/T	0.214843	0.247516	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165756	GAAAGCCTGCTCCTA[C/T]CTCTCGCCAGCTGCG	166979
rs10057041	snp	A/G	0.104938	0.20361	intron-variant	CDC20B	GRCh38.p7	5:55127142	ATATTAAGTCCAATG[A/G]CCTATTTTGTTTTAT	166979
rs10057543	snp	A/G	0.300421	0.244863	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163786	GTGCTGGGATTACAG[A/G]CTGAGCCACGGCTCC	166979
rs10059517	snp	C/T	0.214843	0.247516	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164338	GCTGGAGTGCAGTAG[C/T]GCGTTCTCAGCTCAT	166979
rs10061133	snp	A/G	0.197446	0.244414	intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170716	AAGCAGCCAGCTAAC[A/G]ATACACTGCCTACCT	166979
rs10061396	snp	A/G	0.0744748	0.178019	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112560	AAACCATTAAAGAAG[A/G]GTGTGCATTGCAGAA	166979
rs10067483	snp	A/C	0.0228947	0.104514	intron-variant	CDC20B	GRCh38.p7	5:55129809	ttgaaacaccaccca[A/C]aaatggcaagacaaa	166979
rs10068463	snp	A/G	0.0744748	0.178019	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112788	TGTGTTGATTTTGGG[A/G]GCATAGGGAATAGGT	166979
rs10072079	snp	A/G	0.0543475	0.155628	intron-variant	CDC20B	GRCh38.p7	5:55142446	ATAACAATTGCTAAG[A/G]AGTATCTTGCCAACA	166979
rs10073140	snp	C/T	0.0733688	0.176922	intron-variant	CDC20B	GRCh38.p7	5:55122819	gcatgcccaggcagc[C/T]ggcaaacaagtggtc	166979
rs10075758	snp	C/T	0.243347	0.249911	intron-variant	CDC20B	GRCh38.p7	5:55147215	AACATAAATATGTTA[C/T]GTTTTATATATTTAT	166979
rs10076652	snp	C/T	0.030665	0.119967	intron-variant	CDC20B	GRCh38.p7	5:55129764	agacccaaaccagca[C/T]ggtcaaagtttaaga	166979
rs10078539	snp	C/G	0.24449	0.249939	intron-variant	CDC20B	GRCh38.p7	5:55123328	TTTGCAATTTCAAGA[C/G]GCTCAGAAATTCCCC	166979
rs10079519	snp	G/T	0.0733688	0.176922	intron-variant	CDC20B	GRCh38.p7	5:55125912	ttgaaaaaacaaaat[G/T]gaggataagagacca	166979
rs10079928	snp	C/G	0.0543475	0.155628	intron-variant	CDC20B	GRCh38.p7	5:55135590	ACTCAATTTTTTTCC[C/G]CTTTTTACTGCTGGG	166979
rs10940456	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147186	tgttgttttatatat[A/T]tatatattatataaa	166979
rs10940457	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147188	ttgttttatatattt[A/T]tatattatataaaca	166979
rs10940458	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147194	tatatatttatatat[A/T]atataaacataaata	166979
rs10940459	snp	A/C			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162708	GGAAAGAAAAGCCCA[A/C]GCACATGCCATTGAA	166979
rs11452247	in-del	-/G	0.308414	0.24308	intron-variant	CDC20B	GRCh38.p7	5:55153619	GGGGTGGACTGAAGG[-/G]TTTAGTCTCTGGCCT	166979
rs11741721	snp	G/T			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163687	aattttttgtatttt[G/T]agtagagatggggtt	166979
rs11743987	snp	A/G			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163697	atttttagtagagat[A/G]gggtttcaccgtgtt	166979
rs11744515	snp	C/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55151484	TTGCTCAAAAGTTTC[C/T]TTAGAGCAAAATTCC	166979
rs11746173	snp	A/T	0.0352966	0.128072	intron-variant	CDC20B	GRCh38.p7	5:55150148	aaaaaaataaataaa[A/T]aattaaaaaataaag	166979
rs11748182	snp	C/G			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161409	CATCCTTTGTAACTT[C/G]TAGGAGTTATGCTCC	166979
rs11750703	snp	A/C			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163667	gcacaccaccacacc[A/C]ggctaattttttgta	166979
rs12332290	snp	C/T	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55120664	ACCTGTCACAGCTCT[C/T]CTGGGCCTGCTATCT	166979
rs12518179	snp	C/T	0.489722	0.0709447	intron-variant	CDC20B	GRCh38.p7	5:55117714	TACTTCAAGATGTCA[C/T]CCACTACAGATTTCC	166979
rs12521559	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147149	ttgttttatatattt[A/T]tatattatataaaca	166979
rs12522100	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55147111	tgttttatatattta[C/T]atattatataaacat	166979
rs12522119	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147147	tgttgttttatatat[A/T]tatatattatataaa	166979
rs12522120	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147155	tatatatttatatat[A/T]atataaacataaata	166979
rs12653221	snp	G/T	0.253544	0.249975	intron-variant	CDC20B	GRCh38.p7	5:55157027	CTTGCACCTTATTTG[G/T]ATCCTTTCCAGTGCT	166979
rs12653368	snp	C/T	0.297128	0.245518	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166921	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGTCA	166979
rs12655604	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55146145	atctcaaactgcaac[C/T]taacttgggatgtaa	166979
rs12657420	snp	A/G	0.215144	0.247558	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55167106	GAGTATTCAGCTGTC[A/G]TTCTTGTGAAAAAGG	166979
rs12658369	snp	C/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55127660	CATTTCTAGCTCCTT[C/T]TAAATTGTGAGAATT	166979
rs13353841	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55152139	caccagaaaccagaa[A/G]aggcaaggaatggat	166979
rs13354729	snp	A/G	0.234401	0.249513	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161928	TCTTTTGTTTTTGCT[A/G]TGTGGCTTCTTAACT	166979
rs13356730	snp	A/G	0.234401	0.249513	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161883	ACAGCATAGGCTTTG[A/G]CCTCAAGCTACCTGG	166979
rs13358398	snp	A/G	0.095934	0.196885	intron-variant	CDC20B	GRCh38.p7	5:55114964	ttatcagcctaccac[A/G]CCCTTCATGCCCTAT	166979
rs13359463	snp	C/T	0.244776	0.249945	intron-variant	CDC20B	GRCh38.p7	5:55130645	aactgctaaaggaag[C/T]tcttcaggctaaagg	166979
rs13362299	snp	C/T	0.0607341	0.163335	intron-variant	CDC20B	GRCh38.p7	5:55125472	GAAAAAGGAAATAAA[C/T]ATCTAACAGGTAGAG	166979
rs16883844	snp	A/G	0.0912534	0.193131	intron-variant	CDC20B	GRCh38.p7	5:55119353	AGTAAAAGTTTGTAG[A/G]ACGAAGCTGAGAAGA	166979
rs16883856	snp	A/G	0.0667028	0.170006	intron-variant	CDC20B	GRCh38.p7	5:55128924	TAGACTTCGTTTAAC[A/G]GATCAGTAAAAGTTA	166979
rs16883884	snp	A/C	0.292523	0.246357	intron-variant	CDC20B	GRCh38.p7	5:55151147	CCCAGAAACTGAGGG[A/C]ATCTCTCAAACTTTA	166979
rs17682812	snp	C/T	0.304188	0.244057	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159474	GTTTGTACCCAGTTA[C/T]GTTGTAAAGTGCACT	166979
rs28375271	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55147256	AACATAAATATGTTA[C/T]GTTTTATATATTTAT	166979
rs28521699	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55132585	TTCATTTCTCATCCC[A/C]TTTCTTTTCTTCATG	166979
rs28548699	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55147289	ATTATATAAACATAA[A/G]TATGTTATGTTTTAT	166979
rs28571652	snp	A/T	0.0228947	0.104514	intron-variant	CDC20B	GRCh38.p7	5:55144739	AAAAGTTGCAGTCAG[A/T]GGCTAGTACTGACAA	166979
rs28579660	snp	A/G	0.328382	0.237395	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136380	CCTGGGCAACATGGT[A/G]AAACCCTGCCTCTAC	166979
rs28602836	snp	A/C	0.0146672	0.084371	intron-variant	CDC20B	GRCh38.p7	5:55154347	CAAGTGAGACCCCAT[A/C]TCTAAAATAAAAATC	166979
rs28687802	snp	A/T	0.331642	0.236293	intron-variant	CDC20B	GRCh38.p7	5:55123529	TACTCCTGCTCCACC[A/T]GTTGGTTAGCTGGTG	166979
rs28816080	snp	A/G	0.266273	0.24947	intron-variant	CDC20B	GRCh38.p7	5:55149669	GGAAAATCCATAGGC[A/G]GAGAACACAGATTGG	166979
rs33958487	in-del	-/A/AA/AAA	0.43088	0.172575	intron-variant	CDC20B	GRCh38.p7	5:55138165	AATAGATTTTGAGTT[-/A/AA/AAA]AAAAAAAAAAAAAAA	166979
rs33980647	in-del	-/T	0.0839998	0.186933	intron-variant	CDC20B	GRCh38.p7	5:55121598	TACATTCTACATGTC[-/T]TTTTTTCTGACAAAT	166979
rs34091778	in-del	-/A			intron-variant	CDC20B	GRCh38.p7	5:55137666	AGACATAGGTAAGTC[-/A]AAGTCAAGTTGGAGG	166979
rs34132730	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55147137	AACATAAATATGTTG[G/T]TTTATATATTTATAT	166979
rs34132993	snp	A/T	0.0136462	0.0814671	missense	CDC20B	GRCh38.p7	5:55146694	CTTCTGGGAGGTAGG[A/T]GGTTGACTGCTCTTC	166979
rs34230578	in-del	-/A			utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113883	TTTGGAGCTGGGGAG[-/A]AAAGTCATACGGGAA	166979
rs34235172	in-del	-/C			intron-variant	CDC20B	GRCh38.p7	5:55149880	GCTCACACCTGTAAT[-/C]CCCAACACTTTGGGA	166979
rs34286995	in-del	-/A			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162091	TAAACCATATTAGTC[-/A]AAAAAAAAAAAAAAA	166979
rs34298950	in-del	-/T			intron-variant	CDC20B	GRCh38.p7	5:55116167	AATCTCTTTTTTTTA[-/T]GGAAGACCACTGTCT	166979
rs34343764	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55127604	TTTTAAAGCTCCCCA[G/T]GTGAATTCAATGTGC	166979
rs34351422	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55153050	TCAAGACCAGCCTCG[A/C]CAATGTGGCGAAACC	166979
rs34532996	in-del	-/C			intron-variant	CDC20B	GRCh38.p7	5:55169084	ACTAGGTCAGTGATT[-/C]CTTTATAGAAAATAA	166979
rs34565399	in-del	-/C			intron-variant	CDC20B	GRCh38.p7	5:55123846	CATCATTCTCAATAT[-/C]CCTGTAGACATGAAA	166979
rs34581363	in-del	-/A	0.499987	0.00259581	intron-variant	CDC20B	GRCh38.p7	5:55126467	GTGAGATTCCATGTC[-/A]AAAAAAAAAAAAAAA	166979
rs34645934	in-del	-/C	0.399432	0.200425	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173692	CTCTTCGTTTTCAGA[-/C]AGGCAAGAAAACGTG	166979
rs34776567	in-del	-/T	0.472616	0.113763	intron-variant	CDC20B	GRCh38.p7	5:55122274	TGGAAGTCTTTTCTC[-/T]TTTTTTTTTTTTTAA	166979
rs35334058	in-del	-/T			intron-variant	CDC20B	GRCh38.p7	5:55127064	CACACATGATACATG[-/T]GGCCACCAAGACACT	166979
rs35378535	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55167115	GCTGTCGTTCTTGTG[-/A]AAAAGGAAAAGGACA	166979
rs35428146	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55153726	AATATAGTTAAAATA[C/T]TAAAGGACAGAATAG	166979
rs35551438	in-del	-/C			intron-variant	CDC20B	GRCh38.p7	5:55157236	TGATATATGTATAGT[-/C]CTGAGAATAGAGTTA	166979
rs35647524	in-del	-/A			downstream-variant-500B	CDC20B	GRCh38.p7	5:55112814	TAGGTATGTATTAGT[-/A]AAAAAAATTCATGTC	166979
rs35681848	in-del	-/T			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162943	TATCAACCCTGGCTC[-/T]AACCACTCATTAGCC	166979
rs35686230	snp	C/T	0.0569829	0.158885	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166652	CTATATTGGACAATC[C/T]TCCTTCAGTCTTGTT	166979
rs35770269	snp	A/T	0.382643	0.21191	intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172296	AGGAGTGCAACTAGC[A/T]ACTGTTAAAATCATT	166979
rs35911935	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55153266	AAAAAAAAAAAAAGA[A/C]CAATTTTCAAATTGT	166979
rs35920691	in-del	-/A			intron-variant	CDC20B	GRCh38.p7	5:55126033	TGCTATTATTATAAG[-/A]AAAGGATCTGCTCAT	166979
rs35962660	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55140000	CCACTGCACTCCAGC[C/T]TGAGCAACACCAAAA	166979
rs35963631	in-del	-/A	0.462253	0.132093	intron-variant	CDC20B	GRCh38.p7	5:55143995	TTTATCTCTGTATGG[-/A]AAAAAAAAAAAAAAA	166979
rs35990267	snp	A/G	0.0498117	0.149749	intron-variant	CDC20B	GRCh38.p7	5:55124537	GCTGTATGTACCCAG[A/G]ACTCCAAAGTTACAT	166979
rs56678420	in-del	-/AA			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137193	AAAAAAAAAAAAAAA[-/AA]GAAAGAAAGCACTGA	166979
rs56878092	snp	A/G	0.0707826	0.174302	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136893	TGGGGCTCAGGGTCA[A/G]AAGACTTTGGGAGGC	166979
rs57177129	snp	C/T	0.0322114	0.122752	intron-variant	CDC20B	GRCh38.p7	5:55129623	CACACATCTCAGCCT[C/T]ACCCCTAAATCACCT	166979
rs57281778	in-del	-/A			intron-variant	CDC20B	GRCh38.p7	5:55146367	GTTGCCCATTGGCCA[-/A]CGGTTCTTTGCACAA	166979
rs57826543	in-del	-/C	0.0944967	0.195752	intron-variant	CDC20B	GRCh38.p7	5:55116479	TTTGAGACAGGGTCT[-/C]ACTCTGTCACCCAGA	166979
rs58112193	snp	A/C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130240	GGAAAAATATAATAT[A/C/G]TGAAAAATTCCTTGG	166979
rs58116822	in-del	-/A	0	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162113	AAAAAAAAAAAAAAA[-/A]GGCCGGGCGCGGTGG	166979
rs58433852	snp	C/T	0.197082	0.244335	intron-variant	CDC20B	GRCh38.p7	5:55131006	ATGTGCCTGTGGGCC[C/T]AGCTACTTGGGAGGC	166979
rs58598160	in-del	-/A/AA	0	0	intron-variant	CDC20B	GRCh38.p7	5:55138181	AAAAAAAAAAAAAAA[-/A/AA]GACAGAGCTCACTCT	166979
rs58599409	snp	A/G	0.031825	0.122064	intron-variant	CDC20B	GRCh38.p7	5:55139192	TCAACAGCAACAGTG[A/G]ATACTAGAAAACCAT	166979
rs59266503	snp	A/T	0.0948562	0.196037	intron-variant	CDC20B	GRCh38.p7	5:55155869	TTCAGTACACACAGA[A/T]AAGCCTTTTGGTGGT	166979
rs59652613	snp	A/G	0.0130921	0.0798413	intron-variant	CDC20B	GRCh38.p7	5:55155719	CGCCAGCAGCTGCCC[A/G]CAGGGTCTACAGAGC	166979
rs59934100	in-del	-/ATATGTTATGTTTTATATATTTATATATTATATAAACATAA			intron-variant	CDC20B	GRCh38.p7	5:55147289	ATTATATAAACATAA[lengthTooLong]GTATGTTGTTTTATA	166979
rs60267501	snp	C/T	0.0707826	0.174302	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137131	GCAGTGAACTGAGAT[C/T]GCGCCACTGCACTCC	166979
rs61446128	snp	A/C	0.0599851	0.162463	intron-variant	CDC20B	GRCh38.p7	5:55115603	GAGAATGAGGGAGGA[A/C]AGGAGGTCAGATATG	166979
rs61603090	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55150611	GGTTTTTGAGTAGGA[A/G]TGGGAAGGATGAAAA	166979
rs61742528	snp	C/T	0.00359589	0.0422494	synonymous-codon, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55161023	AAACGTGGCCAGTGA[C/T]TGCCAACTCACAGAC	166979
rs62360381	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55116018	GCAGGCCCCTTATTT[A/T]ATAGGTGAGGGAAAA	166979
rs62360382	snp	C/T	0.24449	0.249939	intron-variant	CDC20B	GRCh38.p7	5:55118914	CACTACCTAACATTG[C/T]ATATATTTGTTTTCT	166979
rs62360383	snp	A/G	0.24449	0.249939	intron-variant	CDC20B	GRCh38.p7	5:55122375	CCCTGGGGCTCAAGC[A/G]ATCCACCTACCTCAG	166979
rs62360384	snp	C/T	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55133011	TTATTATTTATAATC[C/T]ACCTTGGCATATGGT	166979
rs62360385	snp	C/T	0.24449	0.249939	intron-variant	CDC20B	GRCh38.p7	5:55133852	TATTTATTCTGTTAT[C/T]TGGGATTTTAAAACC	166979
rs62360386	snp	A/G	0.24449	0.249939	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136093	GGACTACAGGCACCC[A/G]CCACCACGCCTGGCT	166979
rs62360387	snp	A/T	0	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136578	AAAAAAAAAAAAAAT[A/T]GGACAAGCCATAAAA	166979
rs62360412	snp	C/G			intron-variant	CDC20B	GRCh38.p7	5:55154452	ATCCTGGGAGGTCGA[C/G]GCTGCAGTGAGCCAT	166979
rs62360413	snp	C/T	0.283421	0.247756	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158792	TTGCCTCCCCATACC[C/T]ACCCCTAAAATTCAT	166979
rs62360414	snp	G/T	0.289165	0.246913	intron-variant	CDC20B	GRCh38.p7	5:55169656	ATCTTCCAAAAAAAT[G/T]TAAACCATCCCCCAC	166979
rs62360415	snp	G/T	0.251014	0.249998	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171175	AAAAATTAGCCCAGC[G/T]TGGTGGTGCTGCCTG	166979
rs62360416	snp	C/G	0.208169	0.246476	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173631	TCTCCGGCCTCTGTC[C/G]GTTGGTAATCGCTGT	166979
rs66541009	in-del	-/AA			intron-variant	CDC20B	GRCh38.p7	5:55138166	ATAGATTTTGAGTTA[-/AA]AAAAAAAAAAAAAAA	166979
rs66625938	in-del	-/C			upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173693	TCTTCGTTTTCAGAA[-/C]GGCAAGAAAACGTGG	166979
rs66937344	in-del	-/A	0	0	intron-variant	CDC20B	GRCh38.p7	5:55153263	AAAAAAAAAAAAAAA[-/A]GAACAATTTTCAAAT	166979
rs70989700	in-del	-/A	0	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137177	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	166979
rs70989702	in-del	-/TTTTTTT	0	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172769	TTTTTTTTTTTTTTT[-/TTTTTTT]GGCAACTAGGCACCT	166979
rs71622162	snp	A/G	0.5	0	synonymous-codon	CDC20B	GRCh38.p7	5:55140369	TCCATTAGCCTGCTG[A/G]ACCACGTTCTGGGTT	166979
rs71622163	snp	A/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55141114	GTGGGTGGATGAGCA[A/G]AAAGAACACTTTGGG	166979
rs71622164	snp	A/C	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55157271	AGACAGAACATGAAA[A/C]CAATAATGGTGGATC	166979
rs72764178	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55114765	ACATCTCCTCCTCTT[C/G]TGTGTGTCTTTTCTC	166979
rs72766130	snp	A/C	0.288906	0.246954	intron-variant	CDC20B	GRCh38.p7	5:55117713	GTACTTCAAGATGTC[A/C]CCCACTACAGATTTC	166979
rs72766134	snp	C/T	0.322671	0.239205	intron-variant	CDC20B	GRCh38.p7	5:55127247	CTGTCTCCAACAAGA[C/T]GCTTCTTACCTGCTG	166979
rs72766139	snp	G/T	0.0244538	0.107838	intron-variant	CDC20B	GRCh38.p7	5:55143038	CCTAAATGTAATAAA[G/T]GTACTTAACCAAGAA	166979
rs72766151	snp	A/T	0.303688	0.244167	intron-variant	CDC20B	GRCh38.p7	5:55156897	ATAATAATAAATAAA[A/T]AAATAAGTCATTTAT	166979
rs72766156	snp	C/T			intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163987	TCATTTATGCAGATA[C/T]TAATAGAAGTGAAAA	166979
rs73115893	snp	C/T	0.0603597	0.1629	intron-variant	CDC20B	GRCh38.p7	5:55117361	GACCACAATCCACAG[C/T]CAAAACTATATTTTA	166979
rs73115896	snp	A/G	0.0962929	0.197165	intron-variant	CDC20B	GRCh38.p7	5:55121807	TTTATTTTCTTCTTA[A/G]CAAGAATGAACTTTT	166979
rs73115899	snp	C/T	0.0611083	0.163768	intron-variant	CDC20B	GRCh38.p7	5:55124098	ACTATGGAATTTTTT[C/T]ACTAGAAATAAGAAT	166979
rs73115900	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55124358	TGGCTTCTTATCCAG[C/T]GCCCATCTGGAAGAA	166979
rs73118113	snp	C/T	0.0741063	0.177655	intron-variant	CDC20B	GRCh38.p7	5:55133185	TTCTTTCTAATACAG[C/T]AACATAAAATGTATA	166979
rs73118122	snp	C/G	0.0704125	0.17392	intron-variant	CDC20B	GRCh38.p7	5:55140842	CACAAAAATCTGGGT[C/G]CCATCCCTTTGGGCC	166979
rs73118138	snp	A/T	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55151338	CTGTGGGCCACATTC[A/T]GTGGGCTACATTTGC	166979
rs73118139	snp	A/G	0.0539704	0.155153	intron-variant	CDC20B	GRCh38.p7	5:55151996	GGATGAGCCCTAAAT[A/G]CAATCACATGTATCC	166979
rs73118145	snp	A/G	0.0452528	0.143452	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159805	CTATTGCTGAGCATC[A/G]TACTCCATCCTCTGC	166979
rs73118146	snp	A/G	0.0368353	0.130617	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173656	CGCTGTGTCAGCTAT[A/G]GATGTGAGGCGTGTT	166979
rs74270743	in-del	-/TT			intron-variant	CDC20B	GRCh38.p7	5:55122286	CTCTTTTTTTTTTTT[-/TT]AAGACACAGTCTCAC	166979
rs74442797	snp	C/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55119026	CCAAAAAGTACCTCC[C/G]ACATAATAGATGCTT	166979
rs74561680	snp	A/C	0.0364509	0.129988	intron-variant	CDC20B	GRCh38.p7	5:55157840	CAGTCAACATCCCTG[A/C]CAAAGATAAATCACT	166979
rs74569494	snp	A/C	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55116221	TATAAATGAAAAGCA[A/C]CTTGATTTAGTTGTT	166979
rs74693792	snp	C/T	0.0189856	0.0955633	intron-variant	CDC20B	GRCh38.p7	5:55144485	TCATTTGGACAACCA[C/T]GAGCTTGATAAATTC	166979
rs74763420	snp	C/T	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55139615	GAAGCATAATTATAT[C/T]ATTTGGCTTGATAGT	166979
rs74810060	snp	A/T	0.288646	0.246995	intron-variant	CDC20B	GRCh38.p7	5:55169681	CCCCACCCAAAAAAA[A/T]TCCCCAATATTCTTG	166979
rs75041468	in-del	-/A			intron-variant	CDC20B	GRCh38.p7	5:55128811	AGTGTCAACACTCAC[-/A]GTCTAATAAGCAATA	166979
rs75044480	snp	C/T	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55145871	CTCCTGCTTCTGTCT[C/T]TTTCTTCCATTTCAC	166979
rs75067711	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449B, MIR449C	GRCh38.p7	5:55172654	CATGATACTTTCCTT[A/T]GAAAACACAGATAAC	166979
rs75159460	snp	A/C	0	0	intron-variant	CDC20B	GRCh38.p7	5:55144011	AAAAAAAAAAAAAAA[A/C]CCAGATTTGCACATT	166979
rs75195433	snp	G/T	0.0138799	0.0821421	intron-variant	CDC20B	GRCh38.p7	5:55144099	TTTGCCCGAGCTATG[G/T]TCATCCTGCAAGGAA	166979
rs75288520	snp	A/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55149301	GCAGTCATTGTGGAA[A/G]ATTAGTTTGGTGATA	166979
rs75361334	snp	C/T	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55134148	CTCATCAAAAGACCA[C/T]ACTAAGTTCAAACCA	166979
rs75479297	snp	G/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55134217	GATCAAACTGAGAAT[G/T]ATAAAATCAAAAGAA	166979
rs75483192	snp	A/G	0.0119091	0.0762411	intron-variant, downstream-variant-500B	GPX8, CDC20B	GRCh38.p7	5:55167488	GCATTTGCCAGCTCA[A/G]TGTAAATGCTCATGC	166979
rs75545550	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172752	TGTCAGATTACACTT[C/T]TTTTTTTTTTTTTTT	166979
rs75594005	snp	A/C	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55145907	ATTATTCCATTACTA[A/C]CGCATAATTTTTTCT	166979
rs75609221	snp	A/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55125824	AATATGGGCTCTGGA[A/G]CCAGACCAGCTGGGT	166979
rs75661995	snp	C/T	0.0022618	0.0335527	intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172338	GCAATACACTGCCTA[C/T]CTGACACATCCCAGC	166979
rs75703256	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136558	AGCAAGACTTCATCT[A/C]AAAAAAAAAAAAAAA	166979
rs76372728	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55126969	TCCCTTTAGTACCTA[C/T]TACTTAGCACAGAGA	166979
rs76409372	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137180	AGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAG	166979
rs76432642	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55127689	TTCCAAATCTGGAAA[A/T]CTACCCACAGTTACC	166979
rs76501360	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55129680	TAGTAAAGGCTTTAA[A/G]AAACGAACTGAGATT	166979
rs76635142	snp	A/T	0	0	intron-variant, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172751	TTGTCAGATTACACT[A/T]TTTTTTTTTTTTTTT	166979
rs76668286	snp	A/T			utr-variant-3-prime	CDC20B	GRCh38.p7	5:55114125	GAGTATTTCAACTTG[A/T]TTGATACTCATAAAA	166979
rs76798369	snp	A/C	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55142493	GATGGAGCCACTAAC[A/C]TTGCTGCCACCAGTT	166979
rs76824240	snp	A/T	0.0267878	0.112589	intron-variant	CDC20B	GRCh38.p7	5:55139580	CTTTTAATACTCAGC[A/T]AAACAATTATACTAG	166979
rs76889883	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113258	GCGAACTGATCAAGT[C/T]TGAAGGAACCTTAGC	166979
rs76966008	snp	G/T			utr-variant-3-prime	CDC20B	GRCh38.p7	5:55114127	GTATTTCAACTTGTT[G/T]GATACTCATAAAAAC	166979
rs77009149	snp	A/C	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55131427	CTTGGGTACTCCAAC[A/C]TTTAGAGGTCAGGGA	166979
rs77030260	snp	C/T	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55153487	ATGCCCCCTGATAGA[C/T]ATATGTATTATTTTT	166979
rs77077846	snp	C/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55140725	ATACACCATAGGCCA[C/G]TGATATCAGCAAAGC	166979
rs77213512	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159482	CCAGTTATGTTGTAA[A/C]GTGCACTGCTGACTG	166979
rs77251251	snp	A/G	0.0399052	0.1355	intron-variant	CDC20B	GRCh38.p7	5:55143129	AATTCAACTTTTCCT[A/G]AGAGACCCCAAAGGA	166979
rs77302920	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136559	GCAAGACTTCATCTC[A/C]AAAAAAAAAAAAAAA	166979
rs77365330	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55152568	GCAGCTGTACACTAC[A/G]TACAGCTGTATAGAT	166979
rs77377577	snp	C/T	0.0283406	0.115616	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165060	ATCATTTAACTTGAT[C/T]CCTTATAGGCTGATT	166979
rs77408136	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55144052	ATAGAAACAGTTCCA[C/T]AGTTTTAAATGATAG	166979
rs77427891	snp	C/T	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55114911	GGTCCCAGTCTGAGG[C/T]TCCAGAGATTTAGCA	166979
rs77476120	snp	A/T	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164402	TGTGGCAATGAAGGA[A/T]TTTTTTTTAATGTTA	166979
rs77491383	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55135618	GGGAAACAGACGCTT[G/T]AGGAATAAACATGCA	166979
rs77492347	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55143268	TTTGTAAAGATAAAA[C/T]AGTTATTCTCATTTT	166979
rs77495563	snp	A/G	0.000757725	0.0194496	synonymous-codon	CDC20B	GRCh38.p7	5:55128529	TATGTTTTCAATCCC[A/G]TTGTGGTTCTCCCCA	166979
rs77523524	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113616	CTGAGGAAGCACAGA[A/G]CAGAATAATCAGGAG	166979
rs77593363	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55121062	AGAAAATAAAATTGC[A/C]TTCTATTTATTTATA	166979
rs77778701	snp	G/T	0.0111196	0.0737302	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160486	TTTTGCTGTTACATG[G/T]TCATAAGTTGGAATT	166979
rs77905343	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55132186	GTTGGTCATGACAAT[A/T]CATTCTCTTGGAGAA	166979
rs77905858	snp	A/G	0.0441095	0.141807	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165828	TCACCTGTAAATTGA[A/G]CAGGGGTTGAATGGA	166979
rs78001619	snp	G/T	0.0244538	0.107838	intron-variant	CDC20B	GRCh38.p7	5:55145967	ATTAAAATTCTATAC[G/T]TTGCAAAACAAAAGC	166979
rs78127224	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55119044	ATAATAGATGCTTCA[C/T]AAATAAATAATCAAT	166979
rs78225738	snp	A/G	0.0543475	0.155628	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173908	AGGCGTGAAGAGGGG[A/G]CCAGAAAGCTGAGCA	166979
rs78392493	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55125146	GGACAGATTCAAAAC[A/G]CAGGTGGAGATTCCT	166979
rs78414307	in-del	-/A	0.29278	0.246313	intron-variant	CDC20B	GRCh38.p7	5:55138954	AAAATAAATGACAAT[-/A]AAAAAAATATTAAAA	166979
rs78516858	snp	A/T	0.5	0	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158323	TTAAACAATTCAGCC[A/T]GAGAACACCAAAGTA	166979
rs78616733	snp	C/G	0.00676609	0.0577691	intron-variant	CDC20B	GRCh38.p7	5:55151824	CCCGATTCCAAACTA[C/G]ATTAGGCAGCCAATG	166979
rs78692665	snp	C/T	0.0101479	0.070505	synonymous-codon	CDC20B	GRCh38.p7	5:55128538	AATCCCATTGTGGTT[C/T]TCCCCATTCCAGATG	166979
rs78739422	snp	C/T	0.277778	0.248452	intron-variant	CDC20B	GRCh38.p7	5:55156246	GTATCAAGGGTGGGG[C/T]CAGGTGGACATAATT	166979
rs78770785	snp	C/T	0.0513262	0.151752	intron-variant	CDC20B	GRCh38.p7	5:55151636	TTAACAATATCCTAC[C/T]GCCTTAGCAGGTCTG	166979
rs78868754	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55121999	AAATTTACCAAAGTT[C/T]TCCACTCCTTCTGTA	166979
rs78917332	snp	G/T	0.5	0	missense	CDC20B	GRCh38.p7	5:55119854	CACACAGTCACATCA[G/T]TCTTGGGAGTACCTT	166979
rs78932953	snp	A/G	0.0327778	0.123752	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165941	ACCTGGATTGTTAGC[A/G]AAGAAAACAGAAGCC	166979
rs78980121	snp	C/T	0.0267878	0.112589	intron-variant	CDC20B	GRCh38.p7	5:55169117	TGTTGAAATTTAACC[C/T]TAAAAAAAGACAAGA	166979
rs78991208	snp	A/G/T	0.00518061	0.050666	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136841	GAATAACACAAAAAC[A/G/T]TCCATGATGGCAACA	166979
rs78997595	snp	C/T	0.0189856	0.0955633	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113044	TGATACAGGCTAATG[C/T]CAAGAACTCAAACCC	166979
rs79253431	snp	G/T			upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174867	GCCATTAATTCCACA[G/T]CATACATATACACAG	166979
rs79341083	snp	A/G	0.0244538	0.107838	intron-variant	CDC20B	GRCh38.p7	5:55142414	TTCAGTGATGCTGGG[A/G]TGATGTTCCAGCTGG	166979
rs79399956	snp	A/C	0.5	0	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137176	AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	166979
rs79459970	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	CDC20B, MIR449A	GRCh38.p7	5:55170114	GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAGAAA	166979
rs79482045	snp	C/G	0.00795532	0.062565	intron-variant	CDC20B	GRCh38.p7	5:55127482	ACCCAGCACATCTAG[C/G]CAGCAGTTCTCAATT	166979
rs79495092	snp	A/C	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159908	AGCACCATCTTCTGG[A/C]GAAATATTTTCTTTG	166979
rs79568704	snp	A/G	0.0275645	0.114116	intron-variant	CDC20B	GRCh38.p7	5:55150678	AAACCTTGACTAGGG[A/G]GCAGCAGGTAAGGTG	166979
rs79646005	snp	A/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55115580	CTATGAAAGGAGCCT[A/G]AGGCTAGGAGAATGA	166979
rs79690975	snp	A/C	0	0	intron-variant	CDC20B	GRCh38.p7	5:55144010	AAAAAAAAAAAAAAA[A/C]ACCAGATTTGCACAT	166979
rs79811005	snp	C/T	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55119003	TTCACCTGTGTATCC[C/T]CAGCACCCCAAAAAG	166979
rs79869755	snp	A/C	0.0168055	0.0901129	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113255	ACAGCGAACTGATCA[A/C]GTTTGAAGGAACCTT	166979
rs79876330	snp	A/C	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55144013	AAAAAAAAAAAAAAC[A/C]AGATTTGCACATTTG	166979
rs79988884	snp	A/G	0.0441095	0.141807	intron-variant	CDC20B	GRCh38.p7	5:55154243	TCAAAAGGGTCTGGC[A/G]CAGTGGCTTACACCT	166979
rs80128065	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	CDC20B, MIR449A	GRCh38.p7	5:55170113	AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAGAA	166979
rs80175920	snp	A/C	0.00914312	0.0669923	intron-variant	CDC20B	GRCh38.p7	5:55127103	CAGCAGATCTGAATA[A/C]CTGAGAGGGTGGGAT	166979
rs80248266	snp	C/T	0.0197687	0.0974348	intron-variant	CDC20B	GRCh38.p7	5:55122007	CAAAGTTCTCCACTC[C/T]TTCTGTAAAACATAC	166979
rs80260782	snp	C/T	0.0209421	0.100162	intron-variant	CDC20B	GRCh38.p7	5:55117159	TACCTACTCCTATTT[C/T]AAAGCTTAAAAATTA	166979
rs111217509	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55147358	TATATTTATATATTA[A/T]ATAAACATAAGTATG	166979
rs111273780	snp	C/G			upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173369	GCCTCCGGCCGAGGC[C/G]CGCACCCGGGCGCCA	166979
rs111323130	in-del	-/ACC	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55127641	GGGTTGAGAATTATT[-/ACC]ACATTTCTAGCTCCT	166979
rs111329620	snp	C/T	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55148402	CTACTGACCCAGCAA[C/T]ATCACCTCTAAGAAT	166979
rs111416873	snp	C/G	0.214843	0.247516	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171205	GTAATCCCAGCTACT[C/G]AGGAGGCTGAGACAT	166979
rs111438994	snp	A/G	0.000148993	0.00862985	intron-variant	CDC20B	GRCh38.p7	5:55127228	ATTGTTAATACAAAC[A/G]TAACTGTCTCCAACA	166979
rs111444363	snp	C/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55144234	GATAGTTTAAGATGG[C/T]ATCAGTGAAATACTT	166979
rs111518577	snp	A/G	0.5	0	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160344	GCTTTTATGCCTTTG[A/G]AGTGAAGGATGCAAA	166979
rs111635857	snp	C/T	0.0217236	0.101931	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158906	GATGACGTGCCCAAG[C/T]AGAGGTGGGTTTTGC	166979
rs111684551	snp	C/T	0.00536086	0.0514946	utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173008	CACTCCATCTCCGGC[C/T]GACTTCGCCCTGCCT	166979
rs111701167	snp	C/T	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55124667	TGTCTTTCAGGAGAG[C/T]GATGACAAACTCCAA	166979
rs111773909	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55128721	ATAATACCATCCCCA[C/T]GGTTAGCTGGAAAAT	166979
rs111880486	snp	A/G	0	0	intron-variant	CDC20B	GRCh38.p7	5:55134688	GATCACTTGAGCCAG[A/G]AGCGCCACTCCACAT	166979
rs112037158	snp	A/G	0.0535932	0.154675	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173475	GGTTGGCGGGCGAAG[A/G]AGCGGGTTCTGGGAG	166979
rs112057021	in-del	-/T	0.331325	0.236403	intron-variant	CDC20B	GRCh38.p7	5:55139057	TTGATTTACAATGAG[-/T]TTTTTTTTTTAATGC	166979
rs112139051	snp	A/C	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55158102	AGGTTCTCAAACTTA[A/C]ACGTGTGTATGTGTC	166979
rs112310158	snp	A/G	0.00413789	0.0452971	intron-variant, nc-transcript-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170550	ATATGCAATAAGACA[A/G]CAGTTGCATGTTAGC	166979
rs112314770	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55127530	TCAGCTGGGGAGTCT[A/G]TAACACTATGGATGC	166979
rs112481458	snp	A/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55148993	CAACTGAGAACATGA[A/G]GGTGTGTACTGCATT	166979
rs112505464	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55155378	AGACATCCCAGAAAA[A/G]ACCTGCTGGCGATGC	166979
rs112510692	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55135409	TTTAGGACAAAAGAC[A/G]AGGGAGCTGAGGAAA	166979
rs112521266	snp	C/G	0.0232847	0.105357	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173774	AAATTATTCCCTGCT[C/G]TATACATTGGGAGTA	166979
rs112560342	snp	C/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55147785	ACATATGATATAACA[C/G]TATGTACTGAACATG	166979
rs112564103	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55155496	CTCTGAGTGTGTGCC[A/G]CTCCCACCCACCACC	166979
rs112601145	snp	C/T	0.00993419	0.0697739	intron-variant	CDC20B	GRCh38.p7	5:55140591	ATATTATGAACAGTG[C/T]TGAGCATTTTACATA	166979
rs112705432	snp	C/T	0.0171574	0.0910182	intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172266	TTGGGGGGCGTGCTT[C/T]TGAATGCAACAGAGA	166979
rs112733977	snp	C/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55138786	AAAAAATTAAAAGTA[C/G]GATAGCCAAAATAAA	166979
rs112781656	snp	G/T	0	0	intron-variant	CDC20B	GRCh38.p7	5:55143164	TCACATCATCAAATA[G/T]TTGGAAATGATGACA	166979
rs112830930	snp	C/T			upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174518	AAATTCCAGTAAATC[C/T]TTCAGCAAACATTAA	166979
rs112856433	snp	A/G	0.031825	0.122064	intron-variant	CDC20B	GRCh38.p7	5:55148462	CTCATGCTTGAAATC[A/G]TAGCTCTTTGTGAGG	166979
rs112881078	snp	C/T	0.0256215	0.110247	intron-variant	CDC20B	GRCh38.p7	5:55126463	CAGAGTGAGATTCCA[C/T]GTCAAAAAAAAAAAA	166979
rs112921377	snp	A/C/G	0.00875412	0.0656548	intron-variant	CDC20B	GRCh38.p7	5:55155042	AAGGAAATGCCTGTC[A/C/G]CATAGTTTTGAATGA	166979
rs112985916	in-del	-/G	0.5	0	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136380	CCTGGGCAACATGGT[-/G]AAACCCTGCCTCTAC	166979
rs113040678	snp	C/T	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55148502	GCAGATTGCTTGAGC[C/T]CAGGTGTTCGGGACC	166979
rs113082788	snp	C/T	0.00755907	0.0610114	intron-variant	CDC20B	GRCh38.p7	5:55129426	TTCACACCTTTGCCC[C/T]GAGGACAGGCCCCAT	166979
rs113145409	snp	C/G	0.5	0	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161397	GAGCCAGAATCTCAT[C/G]CTTTGTAACTTCTAG	166979
rs113221751	snp	C/T	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55169352	GTACAGTAGAGAATG[C/T]GAAATATTTCTTATA	166979
rs113241145	snp	A/G	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55154050	CATCTGGAGAACCAC[A/G]TCCAGTCCCAGAACT	166979
rs113400974	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170427	GTATTACTGTATTAT[A/G]AGCTAATGGCAATAA	166979
rs113526736	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55128923	GTAGACTTCGTTTAA[C/T]GGATCAGTAAAAGTT	166979
rs113527284	snp	G/T	0.00151241	0.0274575	intron-variant	CDC20B	GRCh38.p7	5:55143658	CCTACAAGAAAGACA[G/T]TTATCTTTGAATTTG	166979
rs113544222	snp	A/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55140422	TCTGAAAATAAACAC[A/G]CATAAGGAGAATATT	166979
rs113643112	snp	A/G/T	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55119487	CACCCATTCTACACC[A/G/T]CTGGTTTTTCTTCAA	166979
rs113666396	in-del	-/G	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55168851	AGGAATACAAGGACT[-/G]AAAAACTATCTATTG	166979
rs113703917	snp	C/G			upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173368	CGCCTCCGGCCGAGG[C/G]GCGCACCCGGGCGCC	166979
rs113710264	snp	A/T	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55150806	CTGGAGTGCAGCGGC[A/T]CAATCATGGCTCACC	166979
rs113724429	snp	C/T	0.5	0	synonymous-codon	CDC20B	GRCh38.p7	5:55125022	AACACGCCCCAGTCT[C/T]GACCCACTGCGAGTT	166979
rs113758505	snp	C/T	0.0209421	0.100162	intron-variant	CDC20B	GRCh38.p7	5:55139019	ATGGATCTCCAAGAA[C/T]GAAAATATCCACCAA	166979
rs113917144	snp	C/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55128695	ACAACTTTATAGGTA[C/G]GGGGAAAAGAATAAT	166979
rs113964214	snp	A/G	0.00557542	0.0525036	intron-variant	CDC20B	GRCh38.p7	5:55114867	TTCCAGATCCTTAAT[A/G]ACATCTCCAAATGCA	166979
rs113965532	snp	A/C	0.5	0	intron-variant	CDC20B	GRCh38.p7	5:55117745	CAAATGTGTTTGGGA[A/C]ACAACAAATGCTATC	166979
rs114009904	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55155820	CATCTGGACCTGCTG[C/T]TCTGCAGACCTCCCG	166979
rs114021023	snp	A/G	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55129578	AAAGCCAAAAGAAAG[A/G]GATCCTCTGAGTGTG	166979
rs114050396	snp	G/T	0.0130921	0.0798413	intron-variant	CDC20B	GRCh38.p7	5:55152958	GAGAACAATTCTCAG[G/T]GCAGGCACGGTGGCT	166979
rs114062874	snp	C/T	0.00350533	0.0417178	synonymous-codon, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55161140	AGAATCGGAGCCCCG[C/T]CCAAGCAAGGAAGTA	166979
rs114065334	snp	A/C	0.0107246	0.0724382	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137216	AAGCACTGAGAGCTC[A/C]AAATGTAGCATGGAA	166979
rs114100267	snp	A/G	0.0221141	0.102801	intron-variant	CDC20B	GRCh38.p7	5:55153607	TGAATAAATCCCCCC[A/G]GGGTGGACTGAAGGT	166979
rs114104603	snp	A/G	0.0217236	0.101931	intron-variant	CDC20B	GRCh38.p7	5:55147709	TCTGTAGGTATACCA[A/G]TGTAGTTTAGGGAGT	166979
rs114198407	snp	C/G	0.0980852	0.198549	intron-variant	CDC20B	GRCh38.p7	5:55154326	GGAGTTCCAGACCAG[C/G]CTGGGCAAGTGAGAC	166979
rs114213312	snp	G/T	0.260504	0.249779	intron-variant	CDC20B	GRCh38.p7	5:55147039	ATATTTTTGTATATA[G/T]TTATACGTAAAATGT	166979
rs114390454	snp	A/C	0.0788843	0.182262	intron-variant	CDC20B	GRCh38.p7	5:55141421	AACAGGGCAATTATA[A/C]CTTTTACGGACAATA	166979
rs114413175	snp	C/T	0.0130921	0.0798413	intron-variant	CDC20B	GRCh38.p7	5:55168690	TTCTAAAAAAGAAAA[C/T]TTAAAAAAATTTAAG	166979
rs114529695	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55119508	TTTTCTTCAAAATAA[C/G]ATGATTTGTGATGCT	166979
rs114595843	snp	A/T	0.0410537	0.137264	intron-variant	CDC20B	GRCh38.p7	5:55140240	TAAAAATAATATATT[A/T]TAAGATTAGGAAGAA	166979
rs114657161	snp	C/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137458	TTGGATAACATTTGT[C/T]CCCGTGATCCACTGA	166979
rs114660358	snp	A/G	0.0337553	0.125452	intron-variant	CDC20B	GRCh38.p7	5:55156436	TTTGGTTATGAAGTC[A/G]AAAGTTCAAAACTCT	166979
rs114725777	snp	A/C	0.030665	0.119967	intron-variant	CDC20B	GRCh38.p7	5:55135829	TATGTGGCCCAAAAC[A/C]ATCCTTCTTCCAATG	166979
rs114794772	snp	A/C	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55126766	GAAGCCAGCAATCTG[A/C]ATTTTGAGGAGCTCT	166979
rs114987242	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55146261	CACGTGCAAATAAGG[C/G]GAACTGAGCTGTAGC	166979
rs115013696	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113330	AAGGTTACAGGGTGT[A/G]TTTATGGCAGAGCCA	166979
rs115040273	snp	A/G	8.27863e-05	0.00643322	synonymous-codon	CDC20B	GRCh38.p7	5:55128436	TTGCACTTCTCCCTC[A/G]CTGGTGCCAACTGCC	166979
rs115091611	snp	C/T	0.00597247	0.0543191	intron-variant	CDC20B	GRCh38.p7	5:55122567	ATCTAATTCCTCTAC[C/T]TTTGAATGTGGGACT	166979
rs115117963	snp	A/C	0.0103295	0.0711199	intron-variant	CDC20B	GRCh38.p7	5:55148888	GTGAAGAAACTGAGG[A/C]TTAGAGGTCAAGTGA	166979
rs115138214	snp	C/T	0.031825	0.122064	intron-variant	CDC20B	GRCh38.p7	5:55141265	CTGCAAGACTGGCTC[C/T]CCCTTGCCTTCAGGG	166979
rs115168074	snp	C/T	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55142021	AGTAGTTCAATGAAC[C/T]CTTCACAGACTCACT	166979
rs115181301	snp	G/T	0.0376037	0.131863	intron-variant	CDC20B	GRCh38.p7	5:55135970	TTTTTTTGAGACAGA[G/T]TCTCACTCTGTCAGC	166979
rs115216276	snp	A/C	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55118477	GGAAATACACCTGGT[A/C]AGTACATTCTTTATT	166979
rs115292016	snp	C/G	0.0788843	0.182262	intron-variant	CDC20B	GRCh38.p7	5:55154323	CCAGGAGTTCCAGAC[C/G]AGGCTGGGCAAGTGA	166979
rs115460301	snp	C/T	0.0130921	0.0798413	intron-variant	CDC20B	GRCh38.p7	5:55168140	GCCTAGAAACTAATC[C/T]ACCACACTCCTTCCC	166979
rs115462932	snp	C/G	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55141313	TCTTTCTCTGGGCAC[C/G]AGCAAGCCAAGCTGT	166979
rs115522787	snp	C/T	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55145013	CTTGTAAAATCCTTT[C/T]TGTTAATATCTGATT	166979
rs115600713	snp	A/G	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55118565	CCATACCTAGCTGCT[A/G]GAATTAGTTTTGTAA	166979
rs115692904	snp	C/G	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55119649	ATTCAACTATACGCT[C/G]TCTGAGGTAGGGTGG	166979
rs115709575	snp	G/T	0.00199481	0.0315187	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161707	AATATTCTCAAAGAT[G/T]AATATGTCAGCTTAC	166979
rs115805522	snp	A/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55153834	TTAGATTTTTTTTCT[A/T]CATTGCACAGGCATA	166979
rs115936217	snp	A/G	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55129457	TGATGGAGTGCCAGC[A/G]AAGACTCTGACAAAA	166979
rs115980462	snp	A/G	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55132048	TGGGTGACAAAGCAA[A/G]ACTCTGTTTAAAAAA	166979
rs115993370	snp	A/C	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55115830	CTTATTCTTCTACAC[A/C]CATCACTCCCAACAC	166979
rs115997273	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166184	GCAGAACTGCATATG[C/T]CAGCACCACATGGGC	166979
rs116242976	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55133799	GTAGAAGATAGATCT[C/T]GTGAGGAGTACACAG	166979
rs116336340	snp	A/T	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55147940	TCTGTCCATCTTCTC[A/T]AAGAAACACCAGGAG	166979
rs116371799	snp	C/T	0.0123036	0.0774623	intron-variant	CDC20B	GRCh38.p7	5:55125684	AGATAATGAACGCTT[C/T]CTGGATTAATTTAAT	166979
rs116391542	snp	A/C	0.0441095	0.141807	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55174185	CTCTAAGGCAATGTG[A/C]GTTTGTGTGTTTTTC	166979
rs116453449	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55142317	TCACCACTCTCGATG[C/T]TATTTGACTTCTAAC	166979
rs116508854	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55117608	GTTCTTGACCCACAA[A/T]GGAAACACAGCCTCA	166979
rs116521801	snp	A/G	0.0221141	0.102801	intron-variant	CDC20B	GRCh38.p7	5:55156658	AGGCGGGCAGCTCAC[A/G]AGATCAGGAGTTCAT	166979
rs116551354	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55127404	GTTTTCACAGCCCAC[C/T]GTCTTCTCAAAGGCC	166979
rs116617945	snp	A/T	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55118644	GGTCCAGGGAATTGC[A/T]TGTCTTTTGATTAAA	166979
rs116684705	snp	A/G	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55123775	TTGTTTTCAGACAGC[A/G]TATTTTACATATATT	166979
rs116737877	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55126631	AATTTTTCTGGTTAA[A/G]AAGAAGCAGTTAAAC	166979
rs117139946	snp	C/G	0.00914312	0.0669923	intron-variant	CDC20B	GRCh38.p7	5:55149230	AATAAGCATTGGTAA[C/G]GATGCGAAGAAACTG	166979
rs117232689	snp	A/G	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55149693	AGATTGGTCATTGTC[A/G]GGGATTAGGGGAGGA	166979
rs117290678	snp	C/T	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55121283	TAAAGTAGCAAACAT[C/T]GTGTTTATACTATTT	166979
rs117375044	snp	A/C	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55155772	CTTCCATCATGCTGG[A/C]CAAGGCTACCTTCAC	166979
rs118037834	snp	C/T	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55135628	CGCTTGAGGAATAAA[C/T]ATGCACAAAGTTCTA	166979
rs137937126	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55118764	ACAGAGTGTGACAGC[C/T]GAAGAATACAAAGGT	166979
rs137940833	in-del	-/CTTCT	0.00627293	0.0556517	frameshift-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172604	TTGGCGGAATCTTGA[-/CTTCT]CTTCTGCTTCAAGTC	166979
rs137951101	snp	C/T	3.29788e-05	0.00406058	missense	CDC20B	GRCh38.p7	5:55146648	GTCAAGGTCTCTTTC[C/T]CAGGCGGTGTCTTCA	166979
rs137956574	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55144133	ATTATGGGATGCTTG[C/T]TTTGCCAGCATTGAC	166979
rs137978597	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55115104	TTTCAATAAACTAAT[C/T]AGATAAACTGAAGCA	166979
rs138075912	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55140756	CTGCCACAGCTGAAT[A/G]GCCATCTTAAGGTCC	166979
rs138217641	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136734	GTTTCCTTGGCATTT[A/C]TGAAATGAACCACGC	166979
rs138294281	snp	C/G	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55148669	CGCTGCTGCACTCCA[C/G]CCTGGGCGACAAAGT	166979
rs138334108	snp	A/C/G	0.000149257	0.00863772	missense	CDC20B	GRCh38.p7	5:55124813	CTTACCTTGACTGCC[A/C/G]TAGACTGGGTTATGA	166979
rs138334673	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB, downstream-variant-500B	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55171797	TTTTATAAAGACAAG[G/T]TCTCCCTGTGTTGTC	166979
rs138373093	snp	A/G	0.0103295	0.0711199	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166802	GGGAGGCCGAGGCGG[A/G]TGGATCACTTCAGGT	166979
rs138413379	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112518	TTTCTTACAGGTAAT[A/G]CCTGGCATATTAGGA	166979
rs138428700	snp	A/G	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55122460	TTTTAAAGATTCTGC[A/G]GCAGATTGTATTTTC	166979
rs138448688	snp	A/C	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55122846	GGTCCAGCCTCCCAC[A/C]CTTTTAGCTTCCGAT	166979
rs138460198	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55119193	CAGTTTTGTCTTCCT[A/G]TTTCCCTGGGCTGGG	166979
rs138468422	snp	C/T	0.00279162	0.0372561	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160647	AAGTTGTTTGGAAAA[C/T]ACTTATAGTTAGTAA	166979
rs138483465	snp	A/C	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55156194	AGACTTATTCACTAC[A/C]ACAAGAACAGTATAG	166979
rs138693203	snp	A/G	0.00636936	0.0560724	intron-variant	CDC20B	GRCh38.p7	5:55151666	GAGTTTCTGTGATTC[A/G]TCTACCGTCACTCTG	166979
rs138761732	snp	C/T	0.0225045	0.103662	intron-variant	CDC20B	GRCh38.p7	5:55141188	TCAACAGCTTTCTTA[C/T]ACTAGCTCTCTACAC	166979
rs138811807	snp	C/T	0.0227646	0.104231	missense, upstream-variant-2KB	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172622	CTCTTCTGCTTCAAG[C/T]CTTTGGAGAGCACAC	166979
rs138926486	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55125466	GACATAGAAAAAGGA[A/C]ATAAATATCTAACAG	166979
rs138939335	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55114812	CAAGGATACTTGCCA[C/T]TGGATTTAGGGCCAC	166979
rs138949806	snp	A/T	0.0123036	0.0774623	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165751	TGTCAGAAAGCCTGC[A/T]CCTACCTCTCGCCAG	166979
rs138979071	snp	A/G	8.23839e-05	0.00641757	intron-variant, synonymous-codon	CDC20B	GRCh38.p7	5:55120479	ATTTATATCCAAGAT[A/G]TGTAAGCGTCCATCC	166979
rs138988848	snp	G/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55156009	AAAGACATACCTGAG[G/T]CTGGGTAATTTATAA	166979
rs139046434	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174755	ATCCATGTAAATTGG[G/T]ATTTTTAGAATCCAA	166979
rs139108097	snp	A/G	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55132241	AGAACTGTTCCCTTC[A/G]GGGATTTTTCTTTTT	166979
rs139188549	snp	C/T	0.0023933	0.0345097	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163002	ATCTCATCTGCAAAA[C/T]GGGGATGATAATAAT	166979
rs139297833	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55123884	AGCCAGGAATATTGG[A/G]CCAGTACAATGTAGT	166979
rs139417777	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55142368	CTCCTTAACACCATA[A/G]AACAGCTTCCATTAT	166979
rs139430650	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55133118	TTGTTTGACTGATTC[A/G]ATTTACCCATATTTA	166979
rs139560554	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113495	TGTTCAACCTAGCAG[C/T]GGTGTGGAGTCAAGA	166979
rs139560619	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55153566	CAGTGTCCTAGATGG[C/T]ACAAGTCAGCAGATC	166979
rs139561220	snp	A/T	0.00318978	0.0398085	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55112994	AATAAAAGATTTTTT[A/T]AAACAGCTATAATAG	166979
rs139599398	snp	C/T	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55150848	CTCCCAGAGCTCAAG[C/T]GATCCTCCTGCCTCA	166979
rs139614717	snp	A/C	0.00225516	0.0335036	missense	CDC20B	GRCh38.p7	5:55128506	TAGTTACAAGTGAGA[A/C]TTAAGTCTATGTTTT	166979
rs139630234	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55169484	ATATCTATGCTACTT[C/G]GTGGGTCAAAATGCC	166979
rs139633736	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173160	CTCCAGGTCCCCCAC[C/T]CCTCCCACCGCCGCT	166979
rs139671231	snp	C/T	0.00597247	0.0543191	intron-variant	CDC20B	GRCh38.p7	5:55146167	GGGATGTAAACTAAC[C/T]GAAAGCCTAACTTAG	166979
rs139705751	snp	C/T	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55124155	GAACATGGTGGAGCA[C/T]TGATCTAATTCCACA	166979
rs139708732	in-del	-/A			intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136577	AAAAAAAAAAAAAAT[-/A]AGGACAAGCCATAAA	166979
rs139712337	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55119626	CAATCTTAGGCAAAT[G/T]CAGAAACATTCAACT	166979
rs139760853	snp	C/G	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55115941	AAGGATGCCTCCAAG[C/G]GGACATGGGATTGGC	166979
rs139783718	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158393	TTTGTTCTTTACTAG[A/G]AATTATGTTTAAAAG	166979
rs139834697	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137438	TTGCTTTATATACAC[A/G]GCATTTGGATAACAT	166979
rs139932263	snp	G/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55115753	GTACTCTGATACAAG[G/T]TTCTCAGCAGAAAGG	166979
rs140002330	snp	A/T	0.00755907	0.0610114	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162753	GTTACAGCAGCCAGA[A/T]ACGTGGGTGCAATAG	166979
rs140191094	snp	C/G/T	0.000164767	0.00907531	missense	CDC20B	GRCh38.p7	5:55124960	ACAGCTTGCTTGTGG[C/G/T]GAAGTGTTCCAACAT	166979
rs140258031	snp	A/G	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55151251	AGACTTTTCATATGA[A/G]TTTTCCCACTTTTTA	166979
rs140305863	snp	G/T	0.00755907	0.0610114	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163979	TAAAGTTATCATTTA[G/T]GCAGATACTAATAGA	166979
rs140422306	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55145280	CAGTATTAAAGCCTG[C/T]CGTTACATGGGAATT	166979
rs140463370	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55157483	CTTCATTATTTGAAG[C/G]TCTTAAGCCTTAGGA	166979
rs140602628	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55130893	TGGGAGGCCAAGGTG[A/G]GAGGATCACTTGAGC	166979
rs140619698	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55146374	ATTGGCCAACGGTTC[C/T]TTGCACAATTAACTT	166979
rs140640730	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159525	AGAAATTTGAAAAAC[A/T]CTGGACTATAGTTTG	166979
rs140643849	snp	G/T	0.000317087	0.0125874	missense	CDC20B	GRCh38.p7	5:55143514	TTCTCTTTACCTACC[G/T]GCCCTTTTGAGGCAA	166979
rs140665812	snp	C/T	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55121953	CTGAATATACAATAG[C/T]TGCTCTCATTCTTCA	166979
rs140700063	in-del	-/C	0.0429648	0.14013	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160900	ATCAGAGGTTATAGT[-/C]CCCCCCCAAATTGTT	166979
rs140714150	in-del	-/A	0.215144	0.247558	intron-variant	CDC20B	GRCh38.p7	5:55169013	CTTGCTCTTTAATTT[-/A]AAAAAACTAACACAC	166979
rs140776511	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158996	TACTACTTTATTATC[A/G]AGTTCAATTTTTGCT	166979
rs140807412	snp	C/T	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55118011	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	166979
rs140875803	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55141815	TGGGCAACAATTCAT[A/T]GTTGTGGGAGCTGTT	166979
rs140919639	snp	A/C	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55129839	AACTTAAAATGTGAA[A/C]CTAACTAGAACAAAA	166979
rs140959552	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55143310	TTAATCCCAACTCAA[A/C]ATTTTCTCATATATT	166979
rs141008499	snp	A/C	0.00564704	0.0528359	intron-variant	CDC20B	GRCh38.p7	5:55140439	ATAAGGAGAATATTT[A/C]TTTAAAAACATACAT	166979
rs141097109	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165547	CTACCTCAGTATATA[A/G]TTCTGTATACGTATT	166979
rs141219356	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55152083	GACCAAAGAGGCAGT[A/G]ACCGGAGTGATAGGG	166979
rs141262172	in-del	-/TG			intron-variant	CDC20B	GRCh38.p7	5:55135218	AAATAATAAAGTGTA[-/TG]TGTGTGTGTGTGTCT	166979
rs141262315	snp	A/C	0.0115144	0.0749975	intron-variant	CDC20B	GRCh38.p7	5:55132956	ACACCGAAGCTCACT[A/C]AGCTCCTTCTAGTCT	166979
rs141310624	snp	A/G	0.00251872	0.035398	missense	CDC20B	GRCh38.p7	5:55114237	TAGCAATTCCATACA[A/G]AGGCCGTCCCATCAG	166979
rs141381352	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55143816	AAGCCCAGGCTCTCG[C/T]CGCTCCAAAGTCCAT	166979
rs141399778	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55123828	ACTGGGAATTTGGAC[C/T]GATCATCATTCTCAA	166979
rs141417756	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55120606	AAGGAGGTGCACTCA[C/T]GAATGTGATGCACTT	166979
rs141419363	snp	C/T	0.00119737	0.0244387	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162373	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGCCTG	166979
rs141454156	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55118679	TGAGGATTGACTCAT[A/G]CTCTTCCTACACTTG	166979
rs141698836	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55141586	GTAAACATCCTACCT[C/T]GGCCTATCCTTGACC	166979
rs141701152	snp	A/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55115702	ACCAGTACTGCCTAC[A/G]ACTCAATTGAGAGCT	166979
rs141735662	snp	A/G	0.00358779	0.0422022	intron-variant	CDC20B	GRCh38.p7	5:55168330	CAGTGAACAGCCAAG[A/G]GACTGCCCCAAGAGA	166979
rs141811772	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173163	CAGGTCCCCCACTCC[C/T]CCCACCGCCGCTGCA	166979
rs141820709	snp	G/T	0.00914312	0.0669923	intron-variant	CDC20B	GRCh38.p7	5:55156283	ATTATTACAATTCAA[G/T]GTGAGATTTGGGTGG	166979
rs141898628	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173746	AGGGAGAGCGTTGAC[A/G]TATTTATGCAATAAA	166979
rs141929599	snp	A/G	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55147988	CTGTAGTAGTGAACC[A/G]TCCCATGTAGCCATG	166979
rs141931383	snp	C/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55152780	AGACCAGGGACTTTG[C/T]CTTTTATCTTACTAT	166979
rs142043925	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55124706	CTAGAGAAAGAAAAA[A/T]CTCAAAATATTGGCT	166979
rs142064238	snp	A/T	0.0441095	0.141807	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163636	CTCAGCCTCCCGAGT[A/T]GCTGGGATTACAGGT	166979
rs142066315	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137461	GATAACATTTGTCCC[C/T]GTGATCCACTGATGA	166979
rs142147842	snp	A/C	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55120351	GCTTGTTGGGGGCAT[A/C]GGCTCTGTTGTAAAC	166979
rs142234339	snp	A/G	0.000115339	0.00759318	intron-variant, missense	CDC20B	GRCh38.p7	5:55120487	CCAAGATGTGTAAGC[A/G]TCCATCCTTCATTCC	166979
rs142277886	snp	G/T	0.0422008	0.138995	intron-variant	CDC20B	GRCh38.p7	5:55153106	TAGCTGGGCACGGTG[G/T]TGTGTGCCTATAGTC	166979
rs142306128	snp	C/T	0.0130921	0.0798413	intron-variant	CDC20B	GRCh38.p7	5:55151439	AAGATAAACTTAGTT[C/T]GCAGAAAACATGGCA	166979
rs142374060	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55117420	ATGTACTACATAACT[A/G]TAACATAAGTTTCAT	166979
rs142412762	snp	A/G	0.0441095	0.141807	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171073	AATGCCAGCACTTTG[A/G]GAGGCCAAGGTTGGC	166979
rs142428554	snp	C/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB, downstream-variant-500B	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55171884	TGCCGGGATTACAGG[C/G]ATGAGCCACAGTGCC	166979
rs142472226	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113481	ACAGGACTTTTAGAT[A/G]TTCAACCTAGCAGTG	166979
rs142503105	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158816	AATTCATGACCGTTA[C/G]CAACAGCAAAGTTAG	166979
rs142607522	snp	A/C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55154024	TCTGTGTCTCTGCAC[A/C/T]GCTCAGAACACATCT	166979
rs142620160	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55138933	GGATATTTCATAAAG[A/G]AGGAAAAAATAAATG	166979
rs142652948	snp	A/G	0.00914312	0.0669923	intron-variant	CDC20B	GRCh38.p7	5:55135418	AAAGACGAGGGAGCT[A/G]AGGAAAGACATGTCC	166979
rs142655416	snp	C/G			intron-variant	CDC20B	GRCh38.p7	5:55140972	TCCTAAAAACATAGT[C/G]ATAAATGATTAAAGC	166979
rs142691673	snp	A/G	0.00517822	0.0506191	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137228	CTCCAAATGTAGCAT[A/G]GAACAGGACCTTCTA	166979
rs142724357	snp	C/G	0.000153988	0.00877328	missense, intron-variant, splice-donor-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160244	GGGCCCAGAGCAAAG[C/G]TATTTGCAGTTTTGC	166979
rs142746819	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112882	GGCATATGCAGAACA[C/T]ATGAAGGAGCACCAA	166979
rs142766265	snp	A/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55148514	AGCCCAGGTGTTCGG[A/G]ACCAGCCTGGGCAAC	166979
rs142787221	snp	C/T	0.00874735	0.0655527	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162829	TCTTAGCCTGTGTAA[C/T]CAAAAAGGTAACAGT	166979
rs142867992	in-del	-/TT	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55145837	CTTCCTTCCTCTTAC[-/TT]TCTCTTCCTCTCATT	166979
rs142925687	snp	C/T	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55135043	TAAACTATGGACTTT[C/T]GGTGACCATGATGTG	166979
rs142999092	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55146022	ATATACATATATACA[C/T]ATACATTCATACAAT	166979
rs143048755	snp	G/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55123395	AATAATTTTTTATAT[G/T]TATTAATAATCATTT	166979
rs143100758	snp	C/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55119018	CCAGCACCCCAAAAA[C/G]TACCTCCCACATAAT	166979
rs143144203	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55169523	AATGAGAATATATTT[A/G]AGGTCATATTGTATG	166979
rs143148343	snp	A/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55132657	TAAGTGCATTCTGCA[A/T]ACTCTGCCATGAATT	166979
rs143173016	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55145613	TCCTGCCCATCACAC[A/T]GGTGGTTTGGAGCCC	166979
rs143206749	snp	G/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55114583	ACCCATTGGGTGGCT[G/T]AAAACAACAGAAATT	166979
rs143235379	snp	C/T	0.0107246	0.0724382	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161330	CAGGACAATACTTTC[C/T]TATTTCATTTGAAAC	166979
rs143330752	snp	A/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55155835	CTCTGCAGACCTCCC[A/G]TGGCCCCTTCCAGAT	166979
rs143476257	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55152240	TGGACCTCTGGCCTC[C/T]GTAACTAGAAGAGAA	166979
rs143552710	snp	C/T	0.00676609	0.0577691	intron-variant	CDC20B	GRCh38.p7	5:55150438	CCCTGCCTGCAGCCC[C/T]CAGGGGGCGAGGCCG	166979
rs143593161	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55146289	AGCCAATCAGGCCGG[A/C]TCCTACGCACTTCCA	166979
rs143602859	snp	A/G	0.00138052	0.0262365	synonymous-codon, intron-variant, missense, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164062	TATTTTAGATTCTTC[A/G]AAGAAGGAACCAAGG	166979
rs143629208	in-del	-/TA			intron-variant	CDC20B	GRCh38.p7	5:55135234	GTGTGTGTGTGTGTC[-/TA]TATATATATATATAC	166979
rs143644476	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55125790	AAACTATGCAATGCT[A/G]AACAGCATTGTGATT	166979
rs143666801	snp	A/G	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55140153	TGGGACTTGGAGGTA[A/G]GGGTAGTTAGAACAG	166979
rs143787798	snp	A/G	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55131715	ATGGGGAGAGAAATA[A/G]AAAATTATAAGTATA	166979
rs143909865	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55126670	TAGTTCTCAAAGGGA[C/T]GTATCATCAGCATCA	166979
rs143928946	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123978	TGTAATAAATTTGCT[G/T]ACTGTTAATAAGGTA	166979
rs143967833	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55133682	ACAAAGAGCCGGGGA[A/G]GGAAGGAAATGAAGA	166979
rs143989680	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55129264	CCTACAATACATTCC[A/G]TCCCCATGATAAATA	166979
rs144017962	snp	C/G	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55132871	CCTTCTCCTCTATAC[C/G]TTTCCAAGTTCTAAT	166979
rs144021850	in-del	-/AT	0.0543475	0.155628	intron-variant	CDC20B	GRCh38.p7	5:55142746	TTCACTTCCAATTGC[-/AT]ATGAGTTCAGATAAC	166979
rs144070234	snp	C/G	0.0275645	0.114116	intron-variant	CDC20B	GRCh38.p7	5:55169969	ATACAAAAAAATTAG[C/G]CGGGCATGGTAGCAG	166979
rs144188909	snp	C/T	0.00914312	0.0669923	intron-variant	CDC20B	GRCh38.p7	5:55116175	TTTTTTATGGAAGAC[C/T]ACTGTCTATTATTTA	166979
rs144209209	snp	A/C	0.00279162	0.0372561	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113734	TGCATGCTTAACATA[A/C]TGCCTAGCATATAGT	166979
rs144209268	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55153584	AAGTCAGCAGATCCA[C/T]GTTAGCCTGAATAAA	166979
rs144269941	snp	A/G	0.0142736	0.0832652	intron-variant	CDC20B	GRCh38.p7	5:55153752	AATAGAATTCAGAAT[A/G]AAGTCTGGGACAAGG	166979
rs144347290	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55151083	TTTTTTATTTCTCTC[C/T]GCTAAGAAAAAAACC	166979
rs144365507	snp	A/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55149190	CACACCCACGAGGAT[A/G]GCTAGAATTTTTTTA	166979
rs144376943	snp	A/G	0.00835141	0.0640778	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164331	CACCCAGGCTGGAGT[A/G]CAGTAGTGCGTTCTC	166979
rs144412288	snp	C/T	0.000329783	0.0128368	missense	CDC20B	GRCh38.p7	5:55128468	GGCAAGTTCCCTCTT[C/T]TATCCAGGACACAGA	166979
rs144412327	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55157728	TCTCTGGATCACTTG[A/G]TAAGAGTTTCTGTAC	166979
rs144451408	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55141401	GCCAGCTTCTGCACA[A/G]TGTCAACAGGGCAAT	166979
rs144555883	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137085	CCCAAGCTGAGACAG[A/G]AGAATCGCTTGAACC	166979
rs144558322	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55154817	GTAAAGTTTTCCTTA[A/G]AAAAATTAATTTTAG	166979
rs144559225	snp	C/G	1.6489e-05	0.00287128	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160229	CCGCTAAAATGTTCC[C/G]GGCCCAGAGCAAAGG	166979
rs144707266	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55120023	ATGACCCAACCTCCA[A/G]TACAGCTGGGGTAGG	166979
rs144763244	snp	C/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55146438	GTTTTTGTTTTTAAA[C/T]ACATACAGTACCTTT	166979
rs144819903	snp	C/T	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55115918	CACCACACACACACG[C/T]ACCAGTAAAGGATGC	166979
rs144823475	snp	C/T	0.021333	0.101051	intron-variant	CDC20B	GRCh38.p7	5:55141952	GGTGAGTAAAATCAC[C/T]CTGAGTTGAGAACCG	166979
rs144841149	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55141089	AAGGTCATGTTGAGG[C/T]CTGGAGGGAGTGGGT	166979
rs144888812	snp	C/T	0.0103295	0.0711199	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163070	GATCAATTTGAAGCA[C/T]GGAGCGTACATTAAT	166979
rs144930251	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55155654	AGTAGGCAATATGAC[A/C]CACACACTGTCAAGG	166979
rs144949536	snp	C/T	0.00289821	0.0379566	intron-variant, nc-transcript-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170534	CTCTGATGTTCATTG[C/T]ATATGCAATAAGACA	166979
rs145015277	snp	A/G	0.000132655	0.00814308	intron-variant	CDC20B	GRCh38.p7	5:55114356	TTCATACTCCTCCAC[A/G]TTACATGGGCTGCTG	166979
rs145045639	in-del	-/T			intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170693	GTTGTGGCTGCTGAC[-/T]TTGACCCAAGCAGCC	166979
rs145074910	snp	C/T	1.65408e-05	0.00287578	missense	CDC20B	GRCh38.p7	5:55140374	TAGCCTGCTGAACCA[C/T]GTTCTGGGTTACAAA	166979
rs145077113	snp	A/C/G	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55143074	CAAACAACAAGAAAG[A/C/G]CTTAAGGGAAATATT	166979
rs145096410	snp	C/T	4.94385e-05	0.0049716	intron-variant, synonymous-codon	CDC20B	GRCh38.p7	5:55120455	TGGGGTCTGGATGCT[C/T]TTCCCAGCATTTATA	166979
rs145100634	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130285	AGGATAGAGGTGATA[C/G]AGGAAAGAGTAAACT	166979
rs145120281	snp	G/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55125197	GTTCTGCCTGGAGGA[G/T]TCTTTTCACAAGTGA	166979
rs145168670	snp	A/G	0.00848715	0.0645875	missense	CDC20B	GRCh38.p7	5:55127327	GCATATTTCTCAGCC[A/G]CTTTTTAGTTACCAC	166979
rs145208610	snp	A/G	0.000198288	0.00995514	missense	CDC20B	GRCh38.p7	5:55133466	CTGGTTGGAGTATGG[A/G]ATCGTTTATATCACC	166979
rs145246156	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55124304	AAAGGCAGACTAGAG[C/T]CCTCCCTGGCACATT	166979
rs145321611	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55120909	GCCCTTGCAAATTGG[C/T]TCTGAAAATGCAGGC	166979
rs145386958	snp	A/G/T	0.000510699	0.015972	missense	CDC20B	GRCh38.p7	5:55124961	CAGCTTGCTTGTGGC[A/G/T]AAGTGTTCCAACATG	166979
rs145502791	in-del	-/AAG	0.297128	0.245518	intron-variant	CDC20B	GRCh38.p7	5:55135403	TGCTGTTTAGGACAA[-/AAG]AAGACGAGGGAGCTG	166979
rs145527631	in-del	-/C	0.24449	0.249939	intron-variant	CDC20B	GRCh38.p7	5:55142305	CGCTTTGAGTCTTCA[-/C]CACTCTCGATGCTAT	166979
rs145581265	snp	C/G	0.00657837	0.0569729	intron-variant	CDC20B	GRCh38.p7	5:55146594	TCTTTTATTCACGTT[C/G]CAAAACGGGGCTGTG	166979
rs145742942	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55151525	TAAACTTTAAATATA[C/T]ATTTTTAAAATTCTG	166979
rs145770739	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55122795	GATGCTCTGGAATTA[C/T]AAGAAGGAGCATGCC	166979
rs145781904	snp	C/T	0.000399281	0.0141238			GRCh38.p7	5:55148094	CATAAAGAGCTCTTA[C/T]AGAAATTGACAAGTT	166979
rs145810338	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159777	GTAGGTCACATTTAA[C/T]CTACATTCTAAACTA	166979
rs145816473	snp	A/T	1.66081e-05	0.00288163	synonymous-codon	CDC20B	GRCh38.p7	5:55143522	ACCTACCTGCCCTTT[A/T]GAGGCAACACTTTCT	166979
rs145860916	snp	C/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55156193	GAGACTTATTCACTA[C/T]CACAAGAACAGTATA	166979
rs145938890	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137301	AGCTTCCCTGATAAC[A/G]CTCACAACACCACCA	166979
rs145949887	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55134084	TGTCTGCTTTTGGTT[A/C]ATTTTACCCATGACT	166979
rs146070790	snp	A/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55116276	GACACAGTGGCACAC[A/G]CCTGCAGTCCCAGCT	166979
rs146140375	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55123623	GCTTGCTCTGGTTTC[C/T]GGAGACTCTCTCTTA	166979
rs146182381	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55174283	AACCTAAAACTCACT[C/T]CCCTGCTTTCCTTCA	166979
rs146193549	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55169614	ACCTGTGATTTTACA[A/G]AAAATGAAGTGAAAG	166979
rs146312964	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55150514	AAGAGAACTTCTTTC[A/G]CAGAAGACAGGAGCC	166979
rs146347858	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55135605	CCTTTTTACTGCTGG[A/G]AAACAGACGCTTGAG	166979
rs146416940	snp	C/G	0.0189856	0.0955633	intron-variant	CDC20B	GRCh38.p7	5:55131896	ATGGTGAAACTCCAT[C/G]TCTACTAAAAATACA	166979
rs146438904	in-del	-/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164799	CAGGATTTTGTTTTT[-/T]CTTTTTAAGTACAGG	166979
rs146445240	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55129325	ACCTGGAGATCCTGT[A/G]AAGTAAGGAAAAGCA	166979
rs146455578	snp	A/C	0.0119091	0.0762411	intron-variant	CDC20B	GRCh38.p7	5:55125098	AACATGGAGGAAAGC[A/C]TAGTTCAAAGTAAAA	166979
rs146466616	snp	A/G	0.000284941	0.0119327	intron-variant, upstream-variant-2KB, nc-transcript-variant	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172322	TCATTAACAGCCGCT[A/G]GCAATACACTGCCTA	166979
rs146563953	snp	A/C/G	2.00082e-05	0.00316286	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55114209	ACTGAAACCTAGAGG[A/C/G]GCTGGGTGCTAGTAG	166979
rs146687664	snp	A/G	0.00199481	0.0315187	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163916	CTTGAGTTTCACTTC[A/G]TTTGGGTGTTTTGTT	166979
rs146698439	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159513	GGGGTCATGAGTAGA[A/C]ATTTGAAAAACACTG	166979
rs146819666	snp	C/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55143252	TTTTAACCTTTACCT[C/G]TTTGTAAAGATAAAA	166979
rs146927201	snp	A/C	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55118724	AATGGCTCTGCTAAG[A/C]GTTCCCTGTATTCTG	166979
rs147032015	snp	C/T	0.0170251	0.090679	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171261	GAGTTTGCAGTGAGC[C/T]GAGATTGCACCACTG	166979
rs147041984	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166456	AGGAGATTTGAAAGC[A/G]TGTCATACATATTGC	166979
rs147153466	snp	C/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55145137	AAATTCTTCCAAAAA[C/G]AATCAGCATCAAAAC	166979
rs147154351	snp	A/G	0.000263613	0.0114777	synonymous-codon	CDC20B	GRCh38.p7	5:55146686	TCCGGAAGCTTCTGG[A/G]AGGTAGGTGGTTGAC	166979
rs147189931	snp	A/G	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55157399	CCAATGCTGTCCAGC[A/G]CACAAGTTCTCCAAA	166979
rs147298969	snp	G/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55141688	TTGGTATTTTGTTTT[G/T]CTTCCTTGATGTTAT	166979
rs147367813	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112969	CAAAACAACCAACGA[C/T]TCAAACAGTAATAAA	166979
rs147402057	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166985	CAATGAGCCAAGATT[A/G]CACCACTGCACTCCA	166979
rs147404433	snp	G/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55124094	GGAAACTATGGAATT[G/T]TTTTACTAGAAATAA	166979
rs147414097	snp	C/T	0.000399281	0.0141238	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162990	AGGCTTCCATTTATC[C/T]CATCTGCAAAACGGG	166979
rs147443662	in-del	-/T	0.0111196	0.0737302	intron-variant	CDC20B	GRCh38.p7	5:55122133	GTTTTGCCAAACCTG[-/T]TTATGACAGGTGAAC	166979
rs147470963	snp	G/T	0.00159617	0.0282053	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162455	TATTCTGATGACATC[G/T]TCAGTCCTATTTTCA	166979
rs147509306	snp	A/G	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55148535	CCTGGGCAACAAGAC[A/G]AAACCCTGTCTCTAC	166979
rs147560078	snp	A/C	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55121679	TAACTTTTTACAGCA[A/C]CAGCATCCAATGAGT	166979
rs147728811	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55138692	ATTGTCAGAGATATA[A/G]GAGAAGATAGTATAT	166979
rs147787652	in-del	-/T			intron-variant	CDC20B	GRCh38.p7	5:55167970	CCAGGAGGTAGAGGC[-/T]GTAGTGAGCCATGAT	166979
rs147833348	snp	A/G	0.000148301	0.00860978	intron-variant	CDC20B	GRCh38.p7	5:55120413	AAGATGAAGCCCAGA[A/G]GAGATATTAACCTGT	166979
rs147842515	snp	A/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55118492	AAGTACATTCTTTAT[A/T]CTAAGCATCAGCAAA	166979
rs147842883	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158332	TCAGCCAGAGAACAC[C/T]AAAGTAAAATTATCA	166979
rs147852565	snp	C/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55155219	GAATTCAGAGCACCA[C/G]TGCCAAAAATAATTA	166979
rs147948849	snp	C/T	0.0189856	0.0955633	intron-variant	CDC20B	GRCh38.p7	5:55141966	CCCTGAGTTGAGAAC[C/T]GTTAGTATAAAATAA	166979
rs147958782	snp	C/G	0.00151439	0.0274754	intron-variant	CDC20B	GRCh38.p7	5:55139056	TTTGATTTACAATGA[C/G]TTTTTTTTTTTAATG	166979
rs148008399	snp	C/T	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55152769	TACACTCCTTAAGAC[C/T]AGGGACTTTGTCTTT	166979
rs148045992	snp	G/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	GPX8, CDC20B	GRCh38.p7	5:55167347	GTTTAACAATTACAC[G/T]GTATCAATAGTATAT	166979
rs148060474	snp	A/G	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55147781	TATGACATATGATAT[A/G]ACACTATGTACTGAA	166979
rs148099529	snp	C/T	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55125947	ATCATGTTACTGCAG[C/T]GATTAAAATGAAATT	166979
rs148103908	snp	A/G	0.00419355	0.0455981	synonymous-codon	CDC20B	GRCh38.p7	5:55140375	AGCCTGCTGAACCAC[A/G]TTCTGGGTTACAAAG	166979
rs148160140	snp	C/T	0.000478607	0.015462	missense	CDC20B	GRCh38.p7	5:55143571	GCATGAGGTGCCTTG[C/T]AAAAATGGAGAGCAG	166979
rs148220250	snp	A/G	0.0107246	0.0724382	intron-variant	CDC20B	GRCh38.p7	5:55125680	TCAAAGATAATGAAC[A/G]CTTTCTGGATTAATT	166979
rs148223415	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55119021	GCACCCCAAAAAGTA[A/C]CTCCCACATAATAGA	166979
rs148256683	snp	C/T	0.0115144	0.0749975	intron-variant	CDC20B	GRCh38.p7	5:55132944	TCTTTCTGGACAACA[C/T]CGAAGCTCACTAAGC	166979
rs148264209	snp	C/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55143699	CAAGATAATCACTTT[C/G]ATTGTAGGTCTGGCT	166979
rs148269554	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173578	ACTTCTCTTTCTCCA[A/G]CCACACCCTGCCTTT	166979
rs148309182	snp	A/G	0.000399281	0.0141238	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161568	ATTCTCCTCTCTTGT[A/G]ACTAGCATCTGGAGA	166979
rs148377415	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123759	GTTTTGTTTTTGTAT[A/G]TTGTTTTCAGACAGC	166979
rs148425524	snp	C/T	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55141476	TTCCCGGTGTTATAA[C/T]TATAGTGGTGAGCTT	166979
rs148475851	snp	A/G	8.24273e-05	0.00641926	synonymous-codon, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160243	CGGGCCCAGAGCAAA[A/G]GTATTTGCAGTTTTG	166979
rs148539416	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55120334	CTCAATAGAGAAAGA[A/G]AGCTTGTTGGGGGCA	166979
rs148601699	snp	A/T	0.000399281	0.0141238	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163390	CAAAATAAGGTGATT[A/T]TTCACTTTGGGAGGC	166979
rs148697238	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55124561	GTTACATGAAAAAAA[C/T]AGATTTACTTTTTTG	166979
rs148747264	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55154000	GTCCAGAACAGGAGC[A/T]ATCTAAACTCTGTGT	166979
rs148793418	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113395	GCTGAGGACTCCAGA[A/G]GTTGAGGTCAAAGGT	166979
rs148803238	snp	G/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55150382	GTAAGCATTGGTTCA[G/T]TTTGGGTTTTTTACT	166979
rs148855088	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55122535	AGCCTCGCCCATTCC[C/T]TCCATCAATAGGTAC	166979
rs148902887	snp	A/T	0.00164669	0.0286467	missense	CDC20B	GRCh38.p7	5:55146663	TCAGGCGGTGTCTTC[A/T]GCACTGATCCGGAAG	166979
rs148916070	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55139386	GAAGACAACTGTGCA[A/G]CTGGCCAAGAAAGCA	166979
rs148916672	snp	A/T	3.54447e-05	0.00420964	missense	CDC20B	GRCh38.p7	5:55114222	GGGGCTGGGTGCTAG[A/T]AGCAATTCCATACAG	166979
rs148920190	snp	C/T	0.0142736	0.0832652	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166253	CTGCACTGGGAACAA[C/T]CAGGACTGTCCCAGT	166979
rs148970916	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55134937	GCATTTTTAGGGAAA[C/T]GAAACTATTCTGTAT	166979
rs149058507	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55118898	AGAGTCATGGTATTA[C/T]CACTACCTAACATTG	166979
rs149068775	snp	C/G	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55155771	CCTTCCATCATGCTG[C/G]CCAAGGCTACCTTCA	166979
rs149110408	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55114535	TGCTCTTGCCCCTGT[A/G]TCAGTGTCCTGTGGC	166979
rs149160251	snp	A/G	0.00016521	0.00908723	synonymous-codon	CDC20B	GRCh38.p7	5:55133479	GGAATCGTTTATATC[A/G]CCAGAACTTTTAAGA	166979
rs149163981	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55142888	CTAGTTCAAAGCTTT[C/T]GAACTGAAATATGGA	166979
rs149236400	snp	C/T	1.65121e-05	0.00287329	missense	CDC20B	GRCh38.p7	5:55124832	ACTGGGTTATGACTT[C/T]CAGCGGTTGGCCCTG	166979
rs149237876	snp	A/C/T	0.00874735	0.0655527	intron-variant	CDC20B	GRCh38.p7	5:55141312	TTCTTTCTCTGGGCA[A/C/T]GAGCAAGCCAAGCTG	166979
rs149289777	snp	A/G	0.0221141	0.102801	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136912	ACTTTGGGAGGCCAA[A/G]CACAGTGGCTCATGC	166979
rs149389207	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55156677	TCAGGAGTTCATGAC[A/C]AGCCTGACTAATATG	166979
rs149429121	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55115866	TTTGTGCCTGTCCAC[A/G]TGCATGCGCAAGCAC	166979
rs149439990	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55125733	AAATGATGTTCCACA[A/G]TTATTTCAGACATTT	166979
rs149500494	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CDC20B, MIR449B, MIR449C	GRCh38.p7	5:55172711	AATCATAATTTCAGG[C/T]GTGGAATTTTTCTAG	166979
rs149617089	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55148802	GAAACCATATGTACA[G/T]GGTTTTACACGTTTG	166979
rs149647224	snp	A/G	0.00914312	0.0669923	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160828	GGCCTTAACCCAGGC[A/G]TCTAGGTTACAGTTT	166979
rs149719965	snp	C/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55118309	GTTAGAGATAAAAAT[C/G]AGTGTCTAAGAGCTC	166979
rs149774264	snp	A/G	0.000181247	0.00951792	missense	CDC20B	GRCh38.p7	5:55119836	GACACAGTGGGACAG[A/G]TCCACACAGTCACAT	166979
rs149936032	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55151329	AGAGCATGTCTGTGG[A/G]CCACATTCAGTGGGC	166979
rs149969948	snp	G/T	0.00478085	0.0486577	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163037	ACCTCATAGGGTCCC[G/T]GTAAGATTAAAAGAG	166979
rs149975868	snp	C/T	0.000153988	0.00877328	missense	CDC20B	GRCh38.p7	5:55133414	AATGATAACTTACAG[C/T]AGTCATTTCGAAGAC	166979
rs150018562	in-del	-/AT	0.00795532	0.062565	intron-variant	CDC20B	GRCh38.p7	5:55125584	TCACAGCAAACTGCA[-/AT]ATGATTCCTAAGCAG	166979
rs150027446	snp	A/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55138288	GCCTCAATCTCCCAA[A/G]TAGCTGGGATTACAG	166979
rs150038954	in-del	-/CA			intron-variant	CDC20B	GRCh38.p7	5:55115879	ACGTGCATGCGCAAG[-/CA]CACACACACACACGC	166979
rs150302909	snp	C/T	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55155508	GCCGCTCCCACCCAC[C/T]ACCAGCCCAATGCAG	166979
rs150319128	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173167	TCCCCCACTCCTCCC[A/C]CCGCCGCTGCAAGGT	166979
rs150345313	snp	C/G	0.00148554	0.0272133	intron-variant	CDC20B	GRCh38.p7	5:55114325	CCCTGTGGCCTGGGG[C/G]AAGAAGGAAAGACAG	166979
rs150417634	snp	C/T	0.0263992	0.111815	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136411	TAAAAGTACAAAAAT[C/T]GGCCAGGTGTGGTAC	166979
rs150450893	snp	C/T	0.000377822	0.0137393	missense, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55172960	ATCTCCTCTTCCGTG[C/T]GGACCCTCCGAGGCG	166979
rs150493868	snp	A/C	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55131321	CTAGAAAAATGACGA[A/C]AAAACACAATACAAA	166979
rs150567358	snp	C/T	0.00993419	0.0697739	intron-variant	CDC20B	GRCh38.p7	5:55128224	GTGGTGGAAACTAAC[C/T]AGAGTATCCTTACGT	166979
rs150577590	snp	A/G	0.0103295	0.0711199	intron-variant	CDC20B	GRCh38.p7	5:55169353	TACAGTAGAGAATGC[A/G]AAATATTTCTTATAT	166979
rs150661497	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55115709	CTGCCTACGACTCAA[A/T]TGAGAGCTGGAATTT	166979
rs150671352	snp	A/C	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55152822	TGGTATCTAGAAACC[A/C]CATAATGAATAAATA	166979
rs150714957	snp	C/T	0.00100563	0.022401	synonymous-codon	CDC20B	GRCh38.p7	5:55146644	TAGAGTCAAGGTCTC[C/T]TTCTCAGGCGGTGTC	166979
rs150733135	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55137517	TGTTTCATAGTTTAA[A/G]TTCCCTTAAAAGAAT	166979
rs150828492	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123876	AAACTACAAGCCAGG[A/C]ATATTGGGCCAGTAC	166979
rs150939041	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158899	GCAATTAGATGACGT[A/G]CCCAAGTAGAGGTGG	166979
rs150980687	snp	G/T	0.0126979	0.078662	intron-variant	CDC20B	GRCh38.p7	5:55117493	TATTTCACTTTTTAT[G/T]GCTGATCTTGACTCA	166979
rs151033849	snp	C/T	0.00557542	0.0525036	intron-variant	CDC20B	GRCh38.p7	5:55146129	TAGGATGAGTCCCTA[C/T]ATCTCAAACTGCAAC	166979
rs151152852	snp	A/G	0.00159725	0.0282147	missense	CDC20B	GRCh38.p7	5:55124879	TCGTGGGGCCATATT[A/G]TCAGCAGTCCATCAC	166979
rs151193749	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55151181	CTTGTGTTTTAGCCA[C/T]AGCAAGAACACATTG	166979
rs151247368	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113486	ACTTTTAGATGTTCA[A/G]CCTAGCAGTGGTGTG	166979
rs151307348	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55130585	TCATCAACTGGAAGA[C/T]GGAAAATCTAACAGA	166979
rs151318869	snp	C/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171190	GTGGTGGTGCTGCCT[C/G]TAATCCCAGCTACTC	166979
rs180755454	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55124731	TTGGCTTAATGATTT[C/T]CTTTTTATATGTGAA	166979
rs180774876	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55133830	AGATACTACATCATG[C/T]TTTGAATATTTATTC	166979
rs180778936	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55169636	AAGTGAAAGGATTGA[G/T]GTAGATCTTCCAAAA	166979
rs180793642	snp	A/C	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55145971	AAATTCTATACTTTG[A/C]AAAACAAAAGCACAT	166979
rs180807084	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55117235	TAGTCAGGTGGGTGA[A/G]GTCTCTTTAACTGAA	166979
rs180843259	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159407	TTAAAAATGCAACAG[G/T]TGGGGGTGCATCACA	166979
rs180890600	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55153886	CAGTGAAAAAGATTG[A/G]CAGTGTTAGGCAGAC	166979
rs180903821	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55121558	TGCTGTTTGCTCTCA[G/T]AAAGTACATTGTAAT	166979
rs180924842	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165649	ACCCAGCTATGAATG[C/T]ATTTAGAAAGATATT	166979
rs180937602	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55140004	TGCACTCCAGCCTGA[A/G]CAACACCAAAAACAA	166979
rs180956374	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55128699	CTTTATAGGTAGGGG[A/G]AAAAGAATAATACCA	166979
rs181330070	snp	A/C	0.0111196	0.0737302	intron-variant	CDC20B	GRCh38.p7	5:55116124	AATGCTGTGACTATT[A/C]AGACCACACTCCAAA	166979
rs181426960	snp	A/G	0.00597247	0.0543191	intron-variant, downstream-variant-500B	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55170444	GCTAATGGCAATAAT[A/G]TATTATGGTAAATAG	166979
rs181464727	snp	G/T	0.000305639	0.0123582	intron-variant	CDC20B	GRCh38.p7	5:55125053	TACATAACAAAAAAA[G/T]TAAGCCCTGTTGCTA	166979
rs181540054	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166388	CAACCTACAGACTCT[A/G]TGTCAGTGCTGGATT	166979
rs181575501	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55133078	AGATTACAAGCTGGG[A/C]ACATAACAAGTAGAC	166979
rs181578355	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55117059	TCTTCTTTCTGCAAC[G/T]ATAGTCATAAATGAG	166979
rs181594785	snp	A/G	0.0154538	0.0865337	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159214	AGAGACAGGGGTATC[A/G]CTTTCTTGCCCAAGT	166979
rs181598185	snp	C/G	1.64749e-05	0.00287005	missense	CDC20B	GRCh38.p7	5:55146703	GGTAGGTGGTTGACT[C/G]CTCTTCCCCAAAGGA	166979
rs181654966	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55130345	TAAAGAATGTGGAGA[A/C]AAAATTTCTTAAAGA	166979
rs181737937	snp	C/G	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55154212	CCTGGGGTGCTTAGT[C/G]TAGGAGAAAGAAGAT	166979
rs181786675	snp	A/C	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55148179	AGAGATATATAAATG[A/C]CCAAAAGATATTTAA	166979
rs182023868	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55154494	TGCACTGCAGCCTGG[A/G]TGACAGAGTGAGACC	166979
rs182026098	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130839	ATAAAATGCATGACA[A/G]GCCAGACACAGTGTC	166979
rs182036095	snp	A/T			intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171409	AGACAGTAAAATATC[A/T]AGGAGTCGTGATAAT	166979
rs182044182	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55125775	GTGTCGCATTGTTTA[A/G]AACTATGCAATGCTG	166979
rs182140207	snp	A/C	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55149451	GTGCAGACAACCCAA[A/C]CACTCATCAACAGAT	166979
rs182152132	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55126059	CTCATTTTCCTCGTG[G/T]ATAATGAAACTAAAT	166979
rs182175369	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B, MIR449C	GRCh38.p7	5:55172515	AAACTTCCTACAAAT[A/G]CATTATTTACCAAGA	166979
rs182271772	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55143296	TTTCACTTTTTTAAT[G/T]AATCCCAACTCAACA	166979
rs182275938	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55123202	GTCAAAATAAAATAT[C/T]TACAATATATATCAT	166979
rs182291907	snp	C/G	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55121393	CAATCCCATAATATT[C/G]CATCGTGTCGTTATA	166979
rs182295606	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55167961	TGCTTAAGCCCAGGA[A/G]GTAGAGGCTGTAGTG	166979
rs182327441	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165490	CAAATTCTGACCTGA[C/T]GGATGAAAGTGAAGA	166979
rs182510529	snp	A/C	3.29804e-05	0.00406068	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55161082	ACAAAGAGTTTGGAC[A/C]ATCCCACTTCAGCGT	166979
rs182515510	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55135334	TGGCTTCATAGAACA[C/T]ATATTTTTTTATTCT	166979
rs182540876	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136406	TCTACTAAAAGTACA[A/G]AAATTGGCCAGGTGT	166979
rs182554397	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55139088	CAAGCTTTATCATCA[G/T]GAAATCTTAGAACAC	166979
rs182664477	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55155603	GACCAAAATGTTCAT[C/T]GTCTCATGTTTGAAC	166979
rs182782996	snp	G/T	0.00159617	0.0282053	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162514	TATTACCTCACTCAG[G/T]CAATCAAGCTTCTAA	166979
rs182785967	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55126918	ATTCCATAGTATAGA[C/T]ACTGACAGCAATAAA	166979
rs182816197	snp	C/T	0.0158469	0.0875917	upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174418	ATATATCAAAATGTT[C/T]GATAGTCAAATAACT	166979
rs182817661	snp	C/G	0.000281534	0.0118612	intron-variant	CDC20B	GRCh38.p7	5:55119940	TAATGATCAAAAATA[C/G]AGAATTCTTGCAATT	166979
rs182837144	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55117980	AAAAATTAGCCAGGC[A/G]TGGTAGTTGGCGCCT	166979
rs182900349	snp	C/T	0.00279162	0.0372561	intron-variant	CDC20B	GRCh38.p7	5:55131151	ACCTCCCTCAAAAAA[C/T]AATAACAAACAAACA	166979
rs182972305	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55131499	AGTGAACAAAAGACA[C/T]TCTTGGACAAAACCC	166979
rs182979649	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113668	GATAAGGATGAGACC[A/C]TCAGGAGGGGAAAGG	166979
rs182980711	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55140481	ATGTAATGTATAATA[C/T]AGAATTACAACTGGT	166979
rs183106727	snp	C/T	0.000798403	0.0199641	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161648	GGCATTATTAGTTAA[C/T]ATATGTTTGTGGCTA	166979
rs183116583	snp	C/T	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55149986	TAAAAATACAAAAAT[C/T]AGCCAGCCGTGGTGG	166979
rs183118987	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55135825	TCTATATGTGGCCCA[A/G]AACAATCCTTCTTCC	166979
rs183243812	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55156730	AATACAAAAATTAGC[C/T]GGGCATTTTGGCGCG	166979
rs183256129	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131653	GGAAGAGTAGTTTCA[A/G]TTGAATGATGAGACT	166979
rs183491507	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55118957	TCACAAAAGTGTAGG[A/C]TCCCTGAGGGCAAGA	166979
rs183572107	snp	A/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55122227	TTTGGACTAAAGATG[A/T]CTGTTACTTCTATGA	166979
rs183628630	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55156075	GCTAGGGAGTCCTCA[C/T]AATCATGGCAGAAGG	166979
rs183646817	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	GPX8, CDC20B	GRCh38.p7	5:55167698	AAACCCTGTCTCCAC[A/G]AAAAAAATCAAAAAA	166979
rs183659950	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55123153	TGGTGAATTAATGTA[C/T]GGTTTAATAAATCTG	166979
rs183774027	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55127539	GAGTCTATAACACTA[C/T]GGATGCTGATTTAGT	166979
rs183828429	snp	C/G	0.000798403	0.0199641	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163176	CATAAATCTTGAGTG[C/G]TATAAATAGAAAAAA	166979
rs183833710	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136917	GGGAGGCCAAGCACA[A/G]TGGCTCATGCCTATA	166979
rs183836791	snp	A/G	0.00478085	0.0486577	intron-variant	CDC20B	GRCh38.p7	5:55120272	CTCACAAATGAAGAG[A/G]TTTTTACAATAAAAA	166979
rs183863991	snp	C/T	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55142420	GATGCTGGGATGATG[C/T]TCCAGCTGGTATAAC	166979
rs183888133	snp	C/G/T	1.65416e-05	0.00287586	synonymous-codon	CDC20B	GRCh38.p7	5:55125013	GTGATGATAAACACG[C/G/T]CCCAGTCTTGACCCA	166979
rs183911473	snp	A/G	0.0154538	0.0865337	intron-variant	CDC20B	GRCh38.p7	5:55169971	ACAAAAAAATTAGCC[A/G]GGCATGGTAGCAGGC	166979
rs183920791	snp	A/G	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55146036	ATATACATTCATACA[A/G]TCTTTACAAAAGTAA	166979
rs184313745	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158748	AGCAGAATTGAAAGT[A/G]AATGGCTTTTAGGAT	166979
rs184317508	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55132770	CACCTATTCACCAGT[C/T]CCCAATGTATCTTCT	166979
rs184329117	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55116194	GTCTATTATTTAAAA[A/C]ATAATAAACCATATA	166979
rs184332684	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55168588	CTTCCCTCTTTTCTC[A/C]TCATCTCGATAATAT	166979
rs184425681	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55114785	TGTCTTTTCTCCTCT[A/G]TGTGTCTCTCACAAG	166979
rs184462078	snp	A/C	0	0	intron-variant	CDC20B	GRCh38.p7	5:55157577	AAGTTGTATTCATAT[A/C]ATATGGAATTTTGTG	166979
rs184465320	snp	C/G	0.000798403	0.0199641	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163547	GTTTCACTCTTGTCC[C/G]CCAGGCTGGAGGGCA	166979
rs184592796	snp	A/C	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55132206	CTCTTGGAGAAGGAG[A/C]TGAAGGAATAGGGAG	166979
rs184612303	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55129196	AACTCCTGACTGACA[C/T]GTATCAGTATAAAAC	166979
rs184725765	snp	A/C			utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113911	GAAAGAAGTAGAAAT[A/C]TTTGCTATAGATGTT	166979
rs184742768	snp	A/T			intron-variant	CDC20B	GRCh38.p7	5:55153912	CAGACCCCACTACAA[A/T]ATGAGCAAACAGTAT	166979
rs184900926	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55153101	AAAATTAGCTGGGCA[C/T]GGTGGTGTGTGCCTA	166979
rs185122305	snp	C/G	0.00557542	0.0525036	intron-variant	CDC20B	GRCh38.p7	5:55144519	CTAATGTTCCTAGAG[C/G]CTAGTACCTTAAGTA	166979
rs185241116	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123640	GAGACTCTCTCTTAG[C/T]GAAAAGGACTCCCAT	166979
rs185285606	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55121144	AATTGAAATTACTAA[C/T]AATAATCACTTTAAA	166979
rs185294302	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55150437	ACCCTGCCTGCAGCC[C/T]CCAGGGGGCGAGGCC	166979
rs185386485	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55137978	GAGAGGTGGGTTAGT[G/T]AAAAGACTGTCAAGT	166979
rs185394315	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55124548	CCAGGACTCCAAAGT[A/T]ACATGAAAAAAATAG	166979
rs185427568	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55168913	CACTAGAAGCCCAAA[A/C]CCCAGCATCGCCTAT	166979
rs185555738	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55121696	AGCATCCAATGAGTA[C/T]ACTAATTTCACCCTG	166979
rs185558189	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55145752	CTCCTCCTCCTCCTC[C/T]GTCTCCTCCTCTCTT	166979
rs185586413	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165699	ACCAGAGGTCAAGAG[A/G]ATTTGTAGGGATAGC	166979
rs185704686	snp	C/T	0.0158469	0.0875917	intron-variant	CDC20B	GRCh38.p7	5:55118050	CTTGAACTTGGGAGG[C/T]GGAGGTTGCAGTGAG	166979
rs185745382	snp	C/T	0.000247262	0.0111162	synonymous-codon, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55161110	CGTGTTGGCTTTTCC[C/T]TGCAATCAGTTTGGA	166979
rs185747403	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55135397	AACTTGTTGCTGTTT[A/G]GGACAAAAGACGAGG	166979
rs185989708	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55154399	GGCACGCACCTGTGG[C/T]CCAGCTACTTGGGAG	166979
rs186004109	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130419	ATATGTGTAAGTAGA[A/G]TCAGGTCTTAGAAGC	166979
rs186070571	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55121468	TTTTGTTGTATTGTG[A/G]TTTGATTTGTATTGG	166979
rs186089820	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55117491	TCTATTTCACTTTTT[A/T]TTGCTGATCTTGACT	166979
rs186116844	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159666	AGCCTTTTTCAGATA[C/T]TTCCCTGCTCTTTCC	166979
rs186121444	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55133369	AGCACAGGATGCATT[G/T]TGTCATTTCAACTTT	166979
rs186146537	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55125796	TGCAATGCTGAACAG[C/T]ATTGTGATTAACAAT	166979
rs186154730	snp	A/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159321	CATGCCCGGCCTCAG[A/T]TTTTTCCATCTACAG	166979
rs186215631	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55134291	CTTCTGATAAAAGCA[C/T]GAGAGCTTCACAATG	166979
rs186267016	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131003	GATATGTGCCTGTGG[A/G]CCCAGCTACTTGGGA	166979
rs186432082	snp	C/T	0.00517822	0.0506191	intron-variant	CDC20B	GRCh38.p7	5:55155613	TTCATCGTCTCATGT[C/T]TGAACTTTCAACGCC	166979
rs186565461	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171304	GGCAACAAAGTGAGA[C/T]TCTGTCTCAAAAAAA	166979
rs186580357	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55125242	GCAGAGTTTGAAGTC[C/T]AGATTTAAAAATATC	166979
rs186789651	snp	A/G/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55149491	AACAAATCATGGGAC[A/G/T]TATCTACATATGCAA	166979
rs186794627	snp	A/G	0.0103295	0.0711199	intron-variant	CDC20B	GRCh38.p7	5:55126186	TCAAGTTTACATCAG[A/G]TTACTTAAATACATT	166979
rs186819371	snp	C/T	0.000198033	0.00994873	intron-variant, upstream-variant-2KB	CDC20B, MIR449B, MIR449C	GRCh38.p7	5:55172698	AACTATTTAGGAAAA[C/T]CATAATTTCAGGTGT	166979
rs186915023	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55143820	CCAGGCTCTCGTCGC[C/T]CCAAAGTCCATTGCA	166979
rs186928634	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123267	AATAACCATTCTCCA[C/T]CTCTGATTAGGCTGG	166979
rs186939952	snp	A/C	0.00438332	0.0466095	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55167021	GGCAACAGAGCGAGA[A/C]CCCATCTTAAAGACC	166979
rs186949692	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55122667	AATAAAAGGTGTTAA[C/T]GCTTTCACCTTGCTC	166979
rs186951754	snp	A/C/G			intron-variant	CDC20B	GRCh38.p7	5:55168267	GCTATCACTATAATA[A/C/G]TGACAGGTTCAGAGG	166979
rs187114827	snp	C/T			intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171549	AAATGACATTAGTAA[C/T]CGAGTTCTGAAAATG	166979
rs187136098	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55140995	ATTAAAGCAGAGAAG[A/T]TTCTGTTTTGCTTCT	166979
rs187197738	snp	A/C	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55139193	CAACAGCAACAGTGG[A/C]TACTAGAAAACCATA	166979
rs187243670	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55117104	CATGGAATGATGAAA[A/C]CAAGCCAAAGGCCAG	166979
rs187260935	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55149116	AGGGACTGCTCTGCT[A/G]CCATCAGAAATGACA	166979
rs187409767	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165512	AAGTGAAGATGTTTC[A/G]TATGGCAAATTCAGT	166979
rs187652455	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113697	GGGATTCCTACAGAA[C/T]TGATTTTTAGAGAGA	166979
rs187674729	snp	C/T	0.00953873	0.0683987	intron-variant	CDC20B	GRCh38.p7	5:55156142	GGCAAAAGCTTGTGC[C/T]GAAGAACTCCCATTT	166979
rs187679130	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131577	ATAGTTGTTAGGGTT[C/T]GGTATGAAGTCTAAG	166979
rs187761039	snp	A/G	0.00159617	0.0282053	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162961	CCACTCATTAGCCAC[A/G]TGACCTTGTGTCTAG	166979
rs187782683	snp	A/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55119991	GTTAAACTGGTTACA[A/G]GCAGTATGCACTGTC	166979
rs187796177	snp	C/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55123161	TAATGTACGGTTTAA[C/T]AAATCTGGTGAATGT	166979
rs187801864	snp	A/T	0.00398564	0.0444627	intron-variant	CDC20B	GRCh38.p7	5:55127432	GCCTGAGAGCCAATT[A/T]CTGCTGATATTGTTA	166979
rs187806120	snp	C/T	0.00636936	0.0560724	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161863	AAAGGTCATGAGGCA[C/T]ACAGACAGCATAGGC	166979
rs187858175	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55131269	GTACAATAGTAACTC[C/T]ACGTAGACTAAGAAA	166979
rs187951390	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55156913	AAATAAGTCATTTAT[G/T]TAGCACTCAGTTATT	166979
rs188048135	snp	A/C	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136529	ACACTACTGCACTCC[A/C]GCCTGGACGATAGAG	166979
rs188051735	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55150047	GCTGACAAGAGAATC[A/G]CTTGAACCCAGGAGG	166979
rs188099139	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55121530	TTTTTTGTTTTTGTG[C/T]GTGTGTTTTATTTGC	166979
rs188107259	snp	A/C	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55153796	AATTTAATTCAATAA[A/C]GTTGCATGAACAATA	166979
rs188109429	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55127553	ATGGATGCTGATTTA[A/G]TTGGTAGAGTAGAGC	166979
rs188197879	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55168699	AGAAAACTTAAAAAA[A/T]TTTAAGTTGGCATTT	166979
rs188298965	snp	A/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55126954	GATTTCAGCAAAATA[A/T]CCCTTTAGTACCTAT	166979
rs188332770	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB	CDC20B	GRCh38.p7	5:55175167	CCAAGTGATCAAAGT[C/T]AACATCACCATTAGT	166979
rs188605874	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55137689	GTTGGAGGAATGGCC[A/G]TGTAAGTTTATTTCC	166979
rs188607678	snp	G/T	0.000247168	0.0111141	intron-variant	CDC20B	GRCh38.p7	5:55120402	AGATCAAAATGAAGA[G/T]GAAGCCCAGAGGAGA	166979
rs188629473	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	CDC20B, MIR449A	GRCh38.p7	5:55170070	AGTGAGCCGAGATCG[C/T]GCCACTGTACTCCAG	166979
rs188637986	snp	A/T	0.000399281	0.0141238	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163264	GTAGCTCATGCATGT[A/T]ATCCCAGCACTTTGG	166979
rs188644639	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55146551	ACACTCCTTAGTTCT[A/G]CAAGACAAAGATTCT	166979
rs188649993	snp	A/T	0.00348466	0.0415955	intron-variant	CDC20B	GRCh38.p7	5:55125052	TTACATAACAAAAAA[A/T]TTAAGCCCTGTTGCT	166979
rs188687645	snp	A/G	0.0391387	0.134304	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136101	GGCACCCGCCACCAC[A/G]CCTGGCTAATTTTTG	166979
rs188746675	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158924	AGGTGGGTTTTGCAG[G/T]GTTTGTTTGTTTTCA	166979
rs188748739	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55132771	ACCTATTCACCAGTC[A/C]CCAATGTATCTTCTT	166979
rs188757565	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55116431	TAAATATATAATAGA[A/G]CATTACTCTAATGCT	166979
rs188806817	snp	A/T	0.00110845	0.0235159	intron-variant	CDC20B	GRCh38.p7	5:55114342	AGAAGGAAAGACAGT[A/T]CATACTCCTCCACGT	166979
rs188809016	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55142645	CAGTGCACCCTAATT[A/G]TCTCAGTAGGACTCC	166979
rs188837526	snp	A/G	0.00557542	0.0525036	intron-variant	CDC20B	GRCh38.p7	5:55144604	AAAATATGAAATGCT[A/G]GTCAAAGTTTTAGAT	166979
rs188935179	snp	C/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55119251	GCCCCCTTTAACATT[C/T]TAGATGCACAAAAGA	166979
rs189016851	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55165576	TTTGGACCAAAGTTA[C/T]TAGATAAACCAAAAA	166979
rs189088390	snp	C/T	0.00318978	0.0398085	intron-variant	CDC20B	GRCh38.p7	5:55167833	GGCTCCACTGAACTC[C/T]AGGCTGGGCAACAGA	166979
rs189127908	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131876	TCGAGACTAGCCTGG[C/T]CAATATGGTGAAACT	166979
rs189304174	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55139708	TGATATAAGCATGTC[A/G]AGAAACTGATGAAAC	166979
rs189514488	snp	G/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55132432	ATAATCTGCCAAACT[G/T]CTTCTATGTCTGATT	166979
rs189516308	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55124550	AGGACTCCAAAGTTA[C/T]ATGAAAAAAATAGAT	166979
rs189560333	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55145927	TAATTTTTTCTGACT[C/T]TGTATACCAGTAACC	166979
rs189577944	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55142747	TCACTTCCAATTGCA[C/T]ATGAGTTCAGATAAC	166979
rs189610080	snp	A/T	0.00835141	0.0640778	intron-variant	CDC20B	GRCh38.p7	5:55167880	ACAAAAAAAATTTTT[A/T]AATTAGCCAGGTGCG	166979
rs189668826	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55153983	ATTAACAGAAAAATA[A/G]TGTCCAGAACAGGAG	166979
rs189737339	snp	A/G	0.00438332	0.0466095	utr-variant-5-prime, upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173054	TGCTCGACTGCCTCT[A/G]GTTTTCTTCCCAGGT	166979
rs189771467	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55157900	GACTTGGGTTTACAC[A/G]GCTCAAATTACAGCA	166979
rs189793965	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55115893	GCACACACACACACA[C/T]GCACACACACACCAC	166979
rs189899120	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174823	AGAATGCAATTATCT[A/G]TAAAAATACATTTAT	166979
rs189932791	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130280	ATAGCAGGATAGAGG[C/T]GATAGAGGAAAGAGT	166979
rs190087487	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55149585	TTGAAAGCATTATGC[C/T]AAGTGAAAGAAGCCA	166979
rs190174793	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55124209	TGATCTCTTTTCTTA[C/T]GTGTGAGCTTGTGAC	166979
rs190202983	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55117979	CAAAAATTAGCCAGG[C/T]GTGGTAGTTGGCGCC	166979
rs190316273	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55138093	TCTCTGGATAAATAA[A/G]AATGACAATTTTTTA	166979
rs190324265	snp	C/T	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55121708	GTATACTAATTTCAC[C/T]CTGGCTAAAGGTTAC	166979
rs190346779	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55166074	TGTTGGTGCCAGAGC[A/G]CTCTTGCCTTGTATC	166979
rs190357029	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55140140	CACCTATAGAGAATG[A/G]GACTTGGAGGTAGGG	166979
rs190467060	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55118629	TCTCTAATCTGAAAA[A/G]GTCCAGGGAATTGCA	166979
rs190475275	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55117174	TAAAGCTTAAAAATT[A/G]CAACTCTTGAGTAGG	166979
rs190496732	snp	C/T	0.00199481	0.0315187	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55161499	TTCCTTATTACCATC[C/T]TCCTGAAGAATTTAC	166979
rs190508455	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55159334	AGTTTTTTCCATCTA[C/T]AGGTTGTAGTGCATC	166979
rs190513868	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55135656	CTAGCTAGAAGCTTG[C/T]CCAATCTGCAGCCCA	166979
rs190569407	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55121251	GCATCCTCTCTTCTA[C/T]ACATAAAAATATTTT	166979
rs190612331	snp	C/T	0.00438332	0.0466095	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163754	CTTAGGTGATCCACC[C/T]GCCTCAGCCTCCCAA	166979
rs190619529	snp	A/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131090	CAGCCTCCAGCCTGA[A/T]CCACTGCACTCCAGC	166979
rs190714444	snp	A/C	5.18264e-05	0.00509024	intron-variant	CDC20B	GRCh38.p7	5:55133386	GTCATTTCAACTTTT[A/C]ATTCCCAATCTAAAT	166979
rs190716557	snp	A/G	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55169239	AAAGTAGTAAAATGC[A/G]TAAGAATCAAATTAT	166979
rs190845874	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55154440	GAGGATTGCTTGATC[C/T]TGGGAGGTCGACGCT	166979
rs190851875	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55130804	CGTTTACAATTGGAT[G/T]GTTTTCAGTGTATGT	166979
rs190989580	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55149184	CCACTTCACACCCAC[A/G]AGGATGGCTAGAATT	166979
rs191003837	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55125937	AGACCACCTTATCAT[A/G]TTACTGCAGTGATTA	166979
rs191028170	snp	A/G			intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171594	ATATAGGATGTTACC[A/G]CTTGAATACTGAATT	166979
rs191135875	snp	C/T	0.00716266	0.059414	intron-variant	CDC20B	GRCh38.p7	5:55134493	TGGGGCTGGGCACGG[C/T]GGCTCATGCCTGTAA	166979
rs191146783	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55123183	GGTGAATGTAATGTT[C/T]TCAGTCAAAATAAAA	166979
rs191287787	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	CDC20B	GRCh38.p7	5:55136671	TGCCAAAGCACCCCA[C/T]GGATATGCTTACCAG	166979
rs191295413	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113018	ATAATAGTATAATAA[C/T]ACCAAATAGATGATA	166979
rs191301834	snp	A/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55120141	TGAAGAATTTAAGTG[A/T]ACTGTGATCATTGGC	166979
rs191333670	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55155668	CCCACACACTGTCAA[G/T]GTCATTTTCAGGTAA	166979
rs191403032	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55126377	GGTGGTGGGCGCCTG[C/T]AGTCCCAGCTACTCG	166979
rs191411128	snp	A/T	0.000399281	0.0141238	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55160663	ACTTATAGTTAGTAA[A/T]GTGAACATGATGACA	166979
rs191414220	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CDC20B, MIR449A, MIR449B	GRCh38.p7	5:55171332	AAATAAATAAAAAGT[C/T]ACTTAACTATAGCTT	166979
rs191527422	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55131314	GTAATCCCTAGAAAA[A/G]TGACGACAAAACACA	166979
rs191814199	snp	A/G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55144070	TTTTAAATGATAGTG[A/G/T]AAAGAGTATCTGGTT	166979
rs191820477	snp	C/T	0.00199481	0.0315187	intron-variant	CDC20B	GRCh38.p7	5:55123305	GGCTATTTCACAGAA[C/T]ACAAAATTTTGCAAT	166979
rs191851461	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55168281	AGTGACAGGTTCAGA[A/G]GGCAGCGATGGGAAG	166979
rs191853240	snp	A/T	0.00119737	0.0244387	intron-variant	CDC20B	GRCh38.p7	5:55132727	AATCTAAATTTCTGA[A/T]TTTGAATTTTTCTCC	166979
rs191958337	snp	G/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55137836	AGACAGTGGATAAAG[G/T]ATTAATAACTGACCA	166979
rs191959466	snp	C/G	0.00557542	0.0525036	intron-variant	CDC20B	GRCh38.p7	5:55142278	CACGTTTACTCTACA[C/G]GGGAAAGACCTCGCT	166979
rs192011376	snp	A/G	0.00199481	0.0315187	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55163296	AGGCCAAGACAGGAG[A/G]ATCACTTTAGTGCCC	166979
rs192171984	snp	C/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55156657	GAGGCGGGCAGCTCA[C/T]GAGATCAGGAGTTCA	166979
rs192173812	snp	A/G	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55131578	TAGTTGTTAGGGTTC[A/G]GTATGAAGTCTAAGA	166979
rs192215292	snp	A/T	0.000798403	0.0199641	intron-variant	CDC20B	GRCh38.p7	5:55132130	TTGTTTCTTTTTAAT[A/T]TAACAGTTTTTTAAC	166979
rs192277517	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55167203	TGTTTTCTTTGGTGC[A/G]TAGAGAAGAATACTT	166979
rs192285730	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55122958	CATAAAAGATAATGA[A/G]ATGATTATTGTTTTA	166979
rs192506798	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CDC20B	GRCh38.p7	5:55113825	CTAAAGACAGGAAAG[C/T]ATCTCAAAAGGGAAC	166979
rs192576633	snp	C/G			intron-variant	CDC20B	GRCh38.p7	5:55114649	CATGGGGTCACAGGG[C/G]CTGTGCTCCCTAGGG	166979
rs192613470	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55157223	GAAATGTGCCATTTT[C/G]ATATATGTATAGTCT	166979
rs192617449	snp	C/G	0.00159617	0.0282053	intron-variant	CDC20B	GRCh38.p7	5:55127518	TGTGTATTAGGATCA[C/G]CTGGGGAGTCTATAA	166979
rs192664327	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55151781	GCCATCAACTCCTTC[A/G]GGAAGGTGTCTCTGA	166979
rs192715689	snp	A/G	0.00119737	0.0244387	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162999	TTTATCTCATCTGCA[A/G]AACGGGGATGATAAT	166979
rs192780330	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	GPX8, CDC20B	GRCh38.p7	5:55158158	ATTCTGACTCGGGAA[G/T]TCTGGGGTGGGGCCC	166979
rs192830129	snp	A/C	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55127123	GAGGGTGGGATCATA[A/C]CTGATATTAAGTCCA	166979
rs192924825	snp	C/T	0.0023933	0.0345097	intron-variant	CDC20B	GRCh38.p7	5:55145388	AAGAGTTGGCACTTC[C/T]ATTAACATTTGTCTT	166979
rs193059017	snp	A/G	0.00874735	0.0655527	intron-variant	CDC20B	GRCh38.p7	5:55150081	AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC	166979
rs193134942	snp	A/G	0.00438332	0.0466095	intron-variant	GPX8, CDC20B	GRCh38.p7	5:55162209	GAGACTAGCCTGGCC[A/G]ATATGGTGAAACCCC	166979
rs193137296	snp	C/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55119744	TCAGGGCTTTTCCCC[C/G]CAACAACAGCTCACT	166979
rs193157292	snp	A/G	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55124210	GATCTCTTTTCTTAC[A/G]TGTGAGCTTGTGACC	166979
rs193166318	snp	A/C	0.00438332	0.0466095	intron-variant	CDC20B	GRCh38.p7	5:55168899	TTGGGTGATAGGTTC[A/C]CTAGAAGCCCAAACC	166979
rs193288615	snp	A/G	0.0103295	0.0711199	intron-variant, downstream-variant-500B	CDC20B	GRCh38.p7	5:55136105	CCCGCCACCACGCCT[A/G]GCTAATTTTTGTGTG	166979
rs199553657	snp	A/G	0.000596748	0.0172632	intron-variant	CDC20B	GRCh38.p7	5:55127395	AGCATTGGAGTTTTC[A/G]CAGCCCACTGTCTTC	166979
rs199582524	snp	A/C/T	0.00199795	0.0315434	synonymous-codon	CDC20B	GRCh38.p7	5:55124986	AACATGATGCTGGGC[A/C/T]ACCCGAACATCGTGA	166979
rs199620096	in-del	-/GGTCA			intron-variant	CDC20B	GRCh38.p7	5:55126275	CAGGCCGAGGCAGGT[-/GGTCA]GGATCACAAGGTCAG	166979
rs199678706	in-del	-/A			upstream-variant-2KB	CDC20B, MIR449C	GRCh38.p7	5:55173691	GCTCTTCGTTTTCAG[-/A]AAGGCAAGAAAACGT	166979
rs199683421	snp	A/G	0.000164753	0.00907465	missense	CDC20B	GRCh38.p7	5:55146792	GCAACAGGAACCTCT[A/G]CGGACAGCCTCTTCG	166979
rs199708696	snp	A/C			upstream-variant-2KB	CDC20B	GRCh38.p7	5:55174994	CTTAACTTCAGAATG[A/C]TGGAAACAGAAACTC	166979
rs199820748	snp	A/G	8.37402e-05	0.00647017	splice-donor-variant	CDC20B	GRCh38.p7	5:55143511	TTTTTCTCTTTACCT[A/G]CCTGCCCTTTTGAGG	166979
rs199855280	snp	A/C	0.00199792	0.0315431	intron-variant	CDC20B	GRCh38.p7	5:55120600	GCTTCAAAGGAGGTG[A/C]ACTCATGAATGTGAT	166979
rs199869863	snp	A/C			intron-variant	CDC20B	GRCh38.p7	5:55153622	GGGGTGGACTGAAGG[A/C]TTAGTCTCTGGCCTT	166979
rs199870902	snp	C/T			intron-variant	CDC20B	GRCh38.p7	5:55145774	TCCTCTCTTCTCTCT[C/T]TCTCTTTGTCTCTCT	166979
rs199921362	snp	C/T	0.000231934	0.0107663	missense	CDC20B	GRCh38.p7	5:55128435	CTTGCACTTCTCCCT[C/T]GCTGGTGCCAACTGC	166979
rs199929070	in-del	-/CTTTG			intron-variant	CDC20B	GRCh38.p7	5:55145778	CTCTTCTCTCTTTCT[-/CTTTG]TCTCTCTCCCCCCAT	166979
rs199941681	snp	A/G	3.32397e-05	0.00407661	intron-variant	CDC20B	GRCh38.p7	5:55119769	CTCACTTTGCTATAG[A/G]TGCATGGCATTTTAC	166979
rs200007497	snp	C/T	0.000412211	0.0143505	missense	CDC20B	GRCh38.p7	5:55128469	GCAAGTTCCCTCTTT[C/T]ATCCAGGACACAGAA	166979
rs200031751	snp	C/T	3.43525e-05	0.00414428	intron-variant	CDC20B	GRCh38.p7	5:55143671	CATTTATCTTTGAAT[C/T]TGGTTTTTAAAACAA	166979
rs200090685	snp	C/T	0.000399281	0.0141238	intron-variant	CDC20B	GRCh38.p7	5:55168613	TAATATGAGACTAAA[C/T]CACAACTTTAAATGT	166979
rs200102780	in-del	-/ATG			intron-variant	CDC20B	GRCh38.p7	5:55147774	TGTAAAATATGACAT[-/ATG]ATATAACACTATGTA	166979
rs200179703	snp	A/G	0.00199806	0.0315443	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160196	GAATCCTCCAACATG[A/G]AGCCTCTTGCAGCTT	166979
rs200188938	in-del	-/A	0.0225045	0.103662	downstream-variant-500B	CDC20B	GRCh38.p7	5:55112813	TAGGTATGTATTAGT[-/A]AAAAAAAATTCATGT	166979
rs200204975	snp	A/G	0.000718073	0.0189346	stop-gained	CDC20B	GRCh38.p7	5:55133424	TACAGTAGTCATTTC[A/G]AAGACCAGTAATATG	166979
rs200310069	snp	A/G			intron-variant	CDC20B	GRCh38.p7	5:55116300	CCCAGCTACTCAGGA[A/G]GGTCACTTGAAGCAA	166979
rs200376474	snp	C/G	3.29473e-05	0.00405864	missense	CDC20B	GRCh38.p7	5:55146749	CCTAGTTTGACTTTG[C/G]TGCCACCTTGTGGTA	166979
rs200385932	snp	G/T	1.6574e-05	0.00287867	intron-variant	CDC20B	GRCh38.p7	5:55127392	TGTAGCATTGGAGTT[G/T]TCACAGCCCACTGTC	166979
rs200586286	snp	C/T	0.000511024	0.0159766	synonymous-codon, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160342	CAGCTTTTATGCCTT[C/T]GAAGTGAAGGATGCA	166979
rs200610318	in-del	-/TCTC			intron-variant	CDC20B	GRCh38.p7	5:55145767	TGTCTCCTCCTCTCT[-/TCTC]TCTTTCTCTTTGTCT	166979
rs200612430	snp	A/C/T	4.95768e-05	0.00497859	synonymous-codon	CDC20B	GRCh38.p7	5:55125007	AACATCGTGATGATA[A/C/T]ACACGCCCCAGTCTT	166979
rs200678088	snp	C/T	0.00199808	0.0315444	stop-gained	CDC20B	GRCh38.p7	5:55124930	CTGCCATCCGGTGAC[C/T]ACTTCAGAGCACACA	166979
rs200784518	snp	A/G	0.00199792	0.0315431	missense, intron-variant, synonymous-codon, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164099	TTTTGGAAGTATCTT[A/G]TCAACCCTGAGGGTC	166979
rs200843551	snp	A/G	0.00199792	0.0315431	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55161178	TTGCAAGAAAAAACT[A/G]CGGAGTAACTTTCCC	166979
rs200897647	in-del	-/TG	0.0166325	0.0896639	intron-variant	CDC20B	GRCh38.p7	5:55156635	AATCCCAGCACTTTG[-/TG]AGGCCGAGGCGGGCA	166979
rs200898156	snp	C/T	0.000430414	0.0146636	missense	CDC20B	GRCh38.p7	5:55114253	AGGCCGTCCCATCAG[C/T]TGCAGCAGAAAACAC	166979
rs200917900	snp	C/T	8.69044e-05	0.00659125	utr-variant-3-prime, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55164239	CCATTGCGTTTCTAA[C/T]AGAACAGAGAAATGT	166979
rs200952851	snp	C/T	0.000560363	0.0167292	missense	CDC20B	GRCh38.p7	5:55127326	AGCATATTTCTCAGC[C/T]GCTTTTTAGTTACCA	166979
rs200973022	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55150581	GGGGGTCAGTTTTTC[G/T]GTCTTGTAGTTCTTG	166979
rs201050183	in-del	-/GTC			intron-variant	CDC20B	GRCh38.p7	5:55119281	GGATTTAAGGCCCAG[-/GTC]AGGACAGGGCCTGGG	166979
rs201051311	snp	C/T	0.00199792	0.0315431	intron-variant, synonymous-codon	CDC20B	GRCh38.p7	5:55120440	CTGTGAGTTTGTGCT[C/T]GGGGTCTGGATGCTC	166979
rs201110630	in-del	-/A	0.259951	0.249802	intron-variant	CDC20B	GRCh38.p7	5:55147424	TGTTATATTTTATAT[-/A]TTTTTATATTGATAT	166979
rs201143912	snp	C/G	0.000399281	0.0141238	splice-acceptor-variant	CDC20B	GRCh38.p7	5:55128618	CTAGGATATTCAGAT[C/G]TATAAGAAAAGCACT	166979
rs201161421	snp	C/T	1.64792e-05	0.00287042	missense	CDC20B	GRCh38.p7	5:55146673	TCTTCAGCACTGATC[C/T]GGAAGCTTCTGGGAG	166979
rs201240526	snp	A/T	0.00199792	0.0315431	missense, intron-variant, nc-transcript-variant	GPX8, CDC20B	GRCh38.p7	5:55160197	AATCCTCCAACATGG[A/T]GCCTCTTGCAGCTTA	166979
rs201285408	snp	G/T			intron-variant	CDC20B	GRCh38.p7	5:55114715	GGCAGTCATTGATTT[G/T]TGGCCACATCACTCC	166979

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