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

FBXO22

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs335675	snp	C/T	0.170084	0.236883	intron-variant	FBXO22	GRCh38.p7	15:75927944	TTCCTGTCCCCAAAG[C/T]ACCCGTTTGGTAATG	26263
rs335676	snp	C/T	0.13446	0.221699	intron-variant	FBXO22	GRCh38.p7	15:75928171	gtaaattagttcagc[C/T]attgtggaagatagt	26263
rs335677	snp	C/G	0.0777841	0.181223	intron-variant	FBXO22	GRCh38.p7	15:75929247	GGATTTAGAGCCCAC[C/G]TGGATAGACCAGATG	26263
rs335678	snp	A/G	0.0948562	0.196037	intron-variant	FBXO22	GRCh38.p7	15:75929595	GTACATAGCTGCTTC[A/G]TTATTTGTGTTGATT	26263
rs335679	snp	G/T	0.17138	0.237316	intron-variant	FBXO22	GRCh38.p7	15:75929799	TAAGGTGGAGTGCAA[G/T]TCAGTAACATTTCAT	26263
rs335680	snp	C/G	0.029116	0.117091	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930494	TGACAGTTCCCAAAT[C/G]TGTTTGGTCACAAAA	26263
rs335681	snp	A/G	0.329317	0.237084	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930927	CTTCTGGTTATCTCT[A/G]TGAGCTAGATCTGGG	26263
rs335682	snp	C/T	0.029116	0.117091	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902408	cccagccAGTTtttt[C/T]ccatagtctatttat	26263
rs335683	snp	C/T	0.172028	0.23753	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902145	cgttcatacctcccc[C/T]gcccctcagctaact	26263
rs335684	snp	A/G	0.172028	0.23753	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901963	cagtttaccagtgac[A/G]GCATCACtacatttt	26263
rs335685	snp	C/G	0.474992	0.108989	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901945	ATCACTACATTTTTG[C/G]AAATATTTAATTTGT	26263
rs335693	snp	A/G	0.133777	0.221342	intron-variant	FBXO22	GRCh38.p7	15:75921583	acctctgcctcccag[A/G]ttcaagcgattctcc	26263
rs335694	snp	A/G	0.169435	0.236663	intron-variant	FBXO22	GRCh38.p7	15:75921023	ggctgtaacatctag[A/G]tctgtgtaagtacta	26263
rs335695	snp	A/G	0.133435	0.221162	intron-variant	FBXO22	GRCh38.p7	15:75920786	acccaggctgcagta[A/G]agtggcgtgacttca	26263
rs335696	snp	C/T	0.029116	0.117091	intron-variant	FBXO22	GRCh38.p7	15:75919703	GGCCCATGTGACACA[C/T]AGTAAAGCCTGCCTA	26263
rs335697	snp	A/G	0.323671	0.238899	intron-variant	FBXO22	GRCh38.p7	15:75918026	TTCCTTGAGTAATTC[A/G]TTTGTTGTTTACTAT	26263
rs335698	snp	A/C	0.039522	0.134904	intron-variant	FBXO22	GRCh38.p7	15:75917795	AGAACTAACCCGCGT[A/C]TTCTAAAAACTTCTA	26263
rs335699	snp	A/G	0.021333	0.101051	intron-variant	FBXO22	GRCh38.p7	15:75916954	GGTATTTATCATGCT[A/G]TTCTATTATTCTTTC	26263
rs335700	snp	C/T	0.135484	0.22223	intron-variant	FBXO22	GRCh38.p7	15:75916568	tttaagccctaaccc[C/T]ccatgtgactatatt	26263
rs335701	snp	C/T	0.0980852	0.198549	intron-variant	FBXO22	GRCh38.p7	15:75915024	GTAGAGATCACGCCA[C/T]TGCACTCCAACCTTG	26263
rs335702	snp	A/G	0.0298908	0.118541	intron-variant	FBXO22	GRCh38.p7	15:75911748	gagaaagaataaagc[A/G]tattcaaataggaag	26263
rs335703	snp	A/G	0.0298908	0.118541	intron-variant	FBXO22	GRCh38.p7	15:75911377	aggataggaagaatc[A/G]atatcgtgaaaatgc	26263
rs335704	snp	A/T	0.0379877	0.132479	intron-variant	FBXO22	GRCh38.p7	15:75909789	tgtatcgcagaaatt[A/T]aaAAAAAAAAAAAAG	26263
rs335705	snp	C/T	0.0314385	0.121371	intron-variant	FBXO22	GRCh38.p7	15:75908913	AAGAGACAGATAGCA[C/T]GATGGCCTGTGGggc	26263
rs335706	snp	A/G	0.325327	0.238382	intron-variant	FBXO22	GRCh38.p7	15:75908490	CTGAGGCCAGGGTGA[A/G]ACCAGCCTGTCCAAC	26263
rs335707	snp	A/G	0.0399052	0.1355	intron-variant	FBXO22	GRCh38.p7	15:75908421	ACCGGGTATGGCTGC[A/G]TGCGCCTGTAGTCCC	26263
rs335724	snp	A/C	0.0962929	0.197165	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934664	TGAAAAGTTTTGACA[A/C]ATTTTTCTTTGGACT	26263
rs974718	snp	A/G	0.0970103	0.197722	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903623	GTGGCGGGAGCTTGT[A/G]GTTAAAGCTACGAGG	26263
rs1394122	snp	C/T	0.16976	0.236773	intron-variant	FBXO22	GRCh38.p7	15:75925270	TGTAACAACCTGTTA[C/T]GTATTGTTTTATTCC	26263
rs1617498	snp	A/G	0.029116	0.117091	intron-variant	FBXO22	GRCh38.p7	15:75924041	aaggtgcgggttgga[A/G]gatcagattatcagt	26263
rs1695372	snp	A/G	0.0379877	0.132479	intron-variant	FBXO22	GRCh38.p7	15:75924757	ATCTTGCCAACGCTC[A/G]GCAGTGCTAGGTCTG	26263
rs1695379	snp	A/C	0.00453512	0.0474025	utr-variant-3-prime, nc-transcript-variant	FBXO22, NRG4	GRCh38.p7	15:75935263	GGAGTATTAGCTAAA[A/C]ACAAACTAAATTCCT	26263
rs1699263	snp	A/G	0.326506	0.238006	intron-variant	FBXO22	GRCh38.p7	15:75906367	TTAGAGCCAAGGAAT[A/G]TAAGTATGTATATAC	26263
rs1699264	snp	A/T	0	0	intron-variant	FBXO22	GRCh38.p7	15:75906791	TATCATTTGGAAAAA[A/T]TCAAAATGCAAGCAG	26263
rs2201917	snp	A/G	0.499997	0.00119808	intron-variant	FBXO22	GRCh38.p7	15:75912174	cctcaataaaatact[A/G]gcagaccgaatccag	26263
rs2255701	snp	A/G	0.324619	0.238604	intron-variant	FBXO22	GRCh38.p7	15:75904368	TCCAAAGTCCCCGGG[A/G]TAGGTAGGTGTCAGT	26263
rs2455893	snp	A/C	0.039522	0.134904	intron-variant	FBXO22	GRCh38.p7	15:75915431	GCCCTTTAGAAACCA[A/C]AGCTAGAGCAACTGA	26263
rs2455895	snp	A/G	0.039522	0.134904	intron-variant	FBXO22	GRCh38.p7	15:75904333	GCGCTAGTTCGGAAG[A/G]AGAGCCAGATATGGA	26263
rs2460811	snp	A/G	0	0	intron-variant	FBXO22	GRCh38.p7	15:75926212	ATGGCGGGTGGCCCA[A/G]AACATTGGGTCCTTG	26263
rs2648435	snp	G/T	0.134119	0.221521	intron-variant	FBXO22	GRCh38.p7	15:75927424	TTTAGAAGTCATGAG[G/T]TTTCTAAAAGCTAAA	26263
rs2648436	snp	A/C	0.0295035	0.117819	intron-variant	FBXO22	GRCh38.p7	15:75926073	TAAACAGTGTAACCT[A/C]CTGGTGAACCTTTCA	26263
rs2655134	snp	C/T	0	0	intron-variant	FBXO22	GRCh38.p7	15:75916004	gaagtggtgcaacct[C/T]tgcctcccggtttcc	26263
rs2655135	snp	A/G	0.021333	0.101051	intron-variant	FBXO22	GRCh38.p7	15:75915963	ctgcctcagcctccc[A/G]agtagctggaattac	26263
rs3073843	in-del	-/AGA	0.030278	0.119257	intron-variant	FBXO22	GRCh38.p7	15:75904730	TTTCACGGAACGAGA[-/AGA]TGTTCCTTTAATTAA	26263
rs3833815	in-del	-/A	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930265	AATGTGACTCAAGGA[-/A]GTTCTTGAAGGACAA	26263
rs3991408	in-del	-/A/AA/AAA	0.469247	0.120128	intron-variant	FBXO22	GRCh38.p7	15:75904826	aaaaaanaaaaaaaa[-/A/AA/AAA]NGGCCCAACATTTGA	26263
rs4278711	snp	C/G	0	0	intron-variant	FBXO22	GRCh38.p7	15:75928434	cacgtcctttgcagg[C/G]acatggatggagctg	26263
rs4886466	snp	A/G	0.49681	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75907963	AAAAAAAATTTTTTT[A/G]AAGTCCACCAAAAGC	26263
rs4886750	snp	C/T	0.0980852	0.198549	intron-variant	FBXO22	GRCh38.p7	15:75915712	caagagcagcctggc[C/T]gacgtggtgaaaccc	26263
rs7177266	snp	C/T	0.496483	0.0417852	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903599	AAATACAAAAATTAG[C/T]TGGGCGTGGTGGCGG	26263
rs8038182	snp	A/C	0	0	intron-variant	FBXO22	GRCh38.p7	15:75919894	ACTGTGCTGCGCAGC[A/C]CTTCTAATCTTCACC	26263
rs10152926	snp	A/T	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75924114	tatagacagttggat[A/T]tgttggcctggagct	26263
rs10163130	snp	A/G	0.00636936	0.0560724	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932602	AGGCAGCAGCCTCCC[A/G]TCAGTGAATCAGGAG	26263
rs10468061	snp	A/T	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75915460	GCTTAACATTTTTTT[A/T]AAAAAAAGAGTTTAT	26263
rs10468062	snp	A/G	0.0980852	0.198549	intron-variant	FBXO22	GRCh38.p7	15:75915467	ATTTTTTTAAAAAAA[A/G]GAGTTTATTTCTTTT	26263
rs10591372	in-del	-/AAA	0	0	intron-variant	FBXO22	GRCh38.p7	15:75916077	AAAAAAAAAAAAAAA[-/AAA]GTTTATTTCTTTTTT	26263
rs11072563	snp	A/G	0.214541	0.247473	intron-variant	FBXO22	GRCh38.p7	15:75928332	ctattcacagtagca[A/G]agacatggaatcaac	26263
rs11378024	in-del	-/A	0.192715	0.243348	intron-variant	FBXO22	GRCh38.p7	15:75929309	CCAAAAAAAAAAAAA[-/A]TTTTTTTTAAAGATC	26263
rs11636664	snp	C/T	0	0	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902836	TTTCTGCCCAAGATC[C/T]GGCGATCAAATCAGG	26263
rs12437816	snp	C/G	0.49645	0.0419827	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902197	agacaagcaggcata[C/G]tccctgaacatgctg	26263
rs12440944	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75911137	tatatctgttttggt[A/C]ccagtaccatgctgt	26263
rs12441092	snp	C/G	0.00755907	0.0610114	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934008	GATGTgcagagagca[C/G]caattttccttcaat	26263
rs12910038	snp	A/C	0.300169	0.244914	intron-variant	FBXO22	GRCh38.p7	15:75931784	CAGGCAAATATAAAC[A/C]AAAACAAAGCATGAG	26263
rs12912046	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75912926	aatttccctgtaaac[A/T]ctgctttagctgtgt	26263
rs12912173	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75912879	caattttagatcttt[C/T]ctgctttctcctgtg	26263
rs12913306	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75912895	ctgctttctcctgtg[G/T]gcatttagtgctata	26263
rs16967642	snp	C/T	0.00914312	0.0669923	intron-variant	FBXO22	GRCh38.p7	15:75913467	CCTTTCTGCTTCAGA[C/T]TGATTTCTAAACCTT	26263
rs16967653	snp	C/T	0.0256043	0.110214	intron-variant	FBXO22	GRCh38.p7	15:75917226	TGTTTAACTTTTTCT[C/T]TAGTGACTCCAATGG	26263
rs17427842	snp	C/T	0.300169	0.244914	intron-variant	FBXO22	GRCh38.p7	15:75927820	CATCTGCATACCCTT[C/T]GTTTCCTTAAGTAAC	26263
rs17428029	snp	C/T	0.0205511	0.0992634	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933379	AGCTGCTGTGTAACA[C/T]GACCTTAAATAGTCT	26263
rs28411993	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75920080	GAAAAGGTCAGATAG[C/T]GCCCTTAAAACTGAC	26263
rs28579689	snp	A/C	0.0729998	0.176553	downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935510	AAGGCTTAAGCAAGG[A/C]ATATATTTCCATGCC	26263
rs28636006	snp	C/T	0.0633504	0.166319	intron-variant	FBXO22	GRCh38.p7	15:75917083	TTAAATGGCAAACAT[C/T]ATGACACTACACCCT	26263
rs34255722	snp	A/G	0.00164595	0.0286403	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932958	TCCATTTCCAAAGAA[A/G]CCGAATAAGGGAACA	26263
rs34335689	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75926465	CTTTAAGTTGGGGTA[-/G]GGGGAAAGTGATTCT	26263
rs34433647	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75926178	AAAATTCTAGAATAA[-/G]AATCTGTAGTCAGAT	26263
rs34494278	snp	A/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75913866	TTTGACATCACTGGG[A/G]CAAAAGCAATATATG	26263
rs34838406	in-del	-/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75935009	TTATAGCTGAGCCTT[-/T]GGAGCTTGTTATGAA	26263
rs34907942	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75926113	TAAATACTTTTCTGG[-/G]AATTGTTTTTAATGG	26263
rs35005442	in-del	-/A			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902926	GCTGTGCTTCCATTT[-/A]CTTGGTGGTTCTCAG	26263
rs35111597	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75913757	TGTCTAATTTGATCC[-/C]AGGTGACTGTTGATG	26263
rs35139316	in-del	-/T	0.375	0.216506	intron-variant	FBXO22	GRCh38.p7	15:75929515	TGTTTTTTTTTTTTT[-/T]GTTCCCTACTGAGAG	26263
rs35315141	in-del	-/A			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935466	ACTTTCAAAGCAAAA[-/A]TAATTTCTGGGGCTA	26263
rs35364874	snp	A/T	0.364193	0.222396	intron-variant	FBXO22	GRCh38.p7	15:75929323	CCAAAAAAAAAAAAA[A/T]TTTTTTTAAAGATCC	26263
rs35459926	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75918215	ACTTAAACCAGCTGG[-/G]AGTAAAAAATTGTGT	26263
rs35659477	snp	A/G	0.000832505	0.0203853	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932699	ACACCCGAGGCATCA[A/G]TATCCAGAGGGTTCC	26263
rs35775467	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75919820	GAGCATACATGTGTC[-/C]TGGGCTTGAAGTGAC	26263
rs35865885	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75924096	GAGATGGAGATATTG[-/T]ATTATAGACAGTTGG	26263
rs36061952	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75924111	ATTATAGACAGTTGG[-/T]ATATGTTGGCCTGGA	26263
rs36117562	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75921571	AGGCTGAGGCAGGAG[-/G]AATCGCTTGAATCTG	26263
rs55719276	snp	A/G	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75925865	GAAAAATTCCTAAGA[A/G]GATGGGGCAATTCTT	26263
rs55737257	in-del	-/TCT	0.53125	0.20492	intron-variant	FBXO22	GRCh38.p7	15:75904733	ATTAAAGGAACATCT[-/TCT]CGTTCCGTGAAAAGA	26263
rs55782145	snp	A/C	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75923813	ACTGTTGTAGTGGTT[A/C]AGGAAAGAGGAGATG	26263
rs55828994	snp	C/T	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75924001	GCAGCTGTATAGTAC[C/T]ATTGACTAAGGTGAA	26263
rs56311307	snp	A/G	0.0271762	0.113356	intron-variant	FBXO22	GRCh38.p7	15:75929798	TTAAGGTGGAGTGCA[A/G]GTCAGTAACATTTCA	26263
rs56676669	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75904174	CCCAGGCTGGCGGGG[G/T]GGGGGGAGAGACCCT	26263
rs56709997	in-del	-/AA			intron-variant	FBXO22	GRCh38.p7	15:75928740	AACTTAAAAAAAAAA[-/AA]TCAAATTGATAGTCT	26263
rs57011816	snp	A/C	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75926554	CTAGAGAAGATGTTG[A/C]AAGAACACCACTGGA	26263
rs57562463	snp	A/G	0.0119091	0.0762411	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931005	AGGAAGGCCAAGTAC[A/G]TTGAATCCCAGGCAG	26263
rs58314879	in-del	-/T/TT	0	0	intron-variant	FBXO22	GRCh38.p7	15:75904841	TTTTTTTTTTTTTTT[-/T/TT]GAGACGTAGTCTCGC	26263
rs58447748	in-del	-/T	0.0193772	0.0965046	intron-variant	FBXO22	GRCh38.p7	15:75909774	CTTTTTTTTTTTTTT[-/T]AAATTTCTGCGATAC	26263
rs59291761	in-del	-/C	0.169435	0.236663	intron-variant	FBXO22	GRCh38.p7	15:75921642	CTCCAGCCTGGGCGA[-/C]AGCGAGACTCTATCT	26263
rs59354278	snp	G/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903598	AAAATACAAAAATTA[G/T]CTGGGCGTGGTGGCG	26263
rs59613929	in-del	-/AATA			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902396	GCAGCTGCGCCTATA[-/AATA]GACTATGGGAAAAAA	26263
rs59994763	snp	G/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930176	TAGTTCATTCCATTT[G/T]GTAGTAGACATTGGC	26263
rs60155009	snp	C/T	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75925730	CAATGAGGCAGACTT[C/T]ATTTGGGAGACCACT	26263
rs60191258	snp	A/G	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75924285	GTTGGTACTGCTGTA[A/G]TATTATTTTGACATC	26263
rs60378247	snp	A/G	0.0422008	0.138995	intron-variant	FBXO22	GRCh38.p7	15:75909280	GGAGTTTAGGAAAAG[A/G]TTTTGGAGAGGAGGT	26263
rs60677043	in-del	-/TT	0.135484	0.22223	intron-variant	FBXO22	GRCh38.p7	15:75916863	ATTTTTAGGGTAAAC[-/TT]TTAAAAATTGGAATT	26263
rs60817295	snp	C/T	0.0558544	0.157504	intron-variant	FBXO22	GRCh38.p7	15:75925786	AGAGATCAGGCTCAA[C/T]TCCAAATGCACCAAC	26263
rs61087430	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930443	TTCTAATATGCCCAG[G/T]GCTGTGGAAATCTGG	26263
rs61753279	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929903	TTTAGATAACCCTGA[A/G]CTTCGTGTGGTCCTT	26263
rs62027569	snp	G/T			missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903973	TGAGGAATGGAGCCG[G/T]TAGGCTGCTGCGGCG	26263
rs62027570	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75922303	CTGGCTGTCCTTGAC[C/T]AAAGTGTTATGTGGT	26263
rs66480104	in-del	-/AC	0.172997	0.237846	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903258	TTTTCACACACTAAG[-/AC]AATTTTTTAAAAGCA	26263
rs66718032	in-del	-/TCT			intron-variant	FBXO22	GRCh38.p7	15:75904731	TAATTAAAGGAACAT[-/TCT]CTCGTTCCGTGAAAA	26263
rs71140183	in-del	-/A	0.0379877	0.132479	intron-variant	FBXO22	GRCh38.p7	15:75925458	GCCACCAAGAGGGGT[-/A]AAAATAGAACTTTAA	26263
rs71403522	snp	C/T	0.324145	0.238752	intron-variant	FBXO22	GRCh38.p7	15:75915768	AGCCAGGCATGATGG[C/T]GGGCACCTGTAATCC	26263
rs71444939	in-del	-/AAATT	0.324382	0.238678	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901932	GTCTTCTATTAAGAC[-/AAATT]AAATATTTGCAAAAA	26263
rs71444940	in-del	-/T	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75916087	AAAAAAAGTTTATTT[-/T]CTTTTTTTATACTAG	26263
rs72534047	in-del	-/TCT			intron-variant	FBXO22	GRCh38.p7	15:75904732	AATTAAAGGAACWTC[-/TCT]TCGTTCCGTGAAAAG	26263
rs72734553	snp	C/G	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75918726	CCTGGAGGATGTTAA[C/G]TGAAATAAGCCAGGC	26263
rs72734555	snp	C/G	0.156319	0.231784	intron-variant	FBXO22	GRCh38.p7	15:75927006	CTTGTGTTATGGGAG[C/G]ATGTACATCTTAAAG	26263
rs73447002	snp	A/G	0.0103295	0.0711199	intron-variant	FBXO22	GRCh38.p7	15:75916352	ACAGTTTGGGAGGCT[A/G]GAAGTCCAAGATCGG	26263
rs73449022	snp	C/G	0.00993419	0.0697739	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934173	ACGATTTTTTGTGTC[C/G]TTAAAATGGCATGAC	26263
rs74024018	snp	A/G	0.0329836	0.124112	intron-variant	FBXO22	GRCh38.p7	15:75906788	GTTTATCATTTGGAA[A/G]AATTCAAAATGCAAG	26263
rs74024019	snp	A/G	0.0622301	0.165053	intron-variant	FBXO22	GRCh38.p7	15:75908910	TGGGCCCCACAGGCC[A/G]TCATGCTATCTGTCT	26263
rs74024020	snp	A/G	0.0558544	0.157504	intron-variant	FBXO22	GRCh38.p7	15:75909539	GATACTGTGATGCCT[A/G]TTCAAATAAAGCAAG	26263
rs74024021	snp	C/T	0.0448871	0.142929	intron-variant	FBXO22	GRCh38.p7	15:75913319	GAAAAGCTTTTGCTT[C/T]TGTTTTTTTATCATG	26263
rs74024022	snp	A/C	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75913676	GCTTGCTGAGGGAAA[A/C]GGCAGAATGGGTATC	26263
rs74024023	snp	G/T	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75914002	TTATTTAGAGCATTC[G/T]CGTGTTAAATGACTT	26263
rs74664624	snp	G/T	1.64996e-05	0.0028722	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904625	TGGTAGCAGAGGAGC[G/T]TGAGGCAAGTAGCAA	26263
rs74689697	snp	C/T	0.00358779	0.0422022	intron-variant	FBXO22	GRCh38.p7	15:75920502	ACTATCTATATTCAA[C/T]TGGCTCATAATGTAG	26263
rs74819560	snp	A/G	0.0418186	0.138422	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902450	ATACCTGTAATCTCA[A/G]CGCTTTGGGAGGCGG	26263
rs75334901	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75908008	TGCCATTTGTAACTT[A/C]TTTGAACAGTGGAAT	26263
rs75552790	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75906314	TCTCTAAGTGTACTC[C/T]TTGCCATTGAGGGAT	26263
rs75629444	snp	C/T	0.0737376	0.17729	intron-variant	FBXO22	GRCh38.p7	15:75928941	ACTCTCACCTGCTTC[C/T]GTGGAGGAGGTGAAT	26263
rs75781160	snp	C/T	0.0535932	0.154675	intron-variant	FBXO22	GRCh38.p7	15:75918969	ATTCTTTTTTTTGTT[C/T]GTTTTGGAGACAGAG	26263
rs75830440	snp	A/G	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75920525	TAATGTAGAACTCCT[A/G]CATTAATTTTATTCA	26263
rs75847036	snp	A/G	0.0252325	0.109451	intron-variant	FBXO22	GRCh38.p7	15:75926556	AGAGAAGATGTTGAA[A/G]GAACACCACTGGAGA	26263
rs75881136	snp	C/T	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75914769	TTAGATACCTGGATT[C/T]GAATGCCGGCTGTAC	26263
rs76008182	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903181	GCCATTTTACTCATT[C/G]GAAACTTTAAACCTG	26263
rs76253651	snp	G/T	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75929514	TCTGTGTAAACCAGT[G/T]TTTTTTTTTTTTTGT	26263
rs76581427	snp	A/G/T	0.0410537	0.137264	intron-variant	FBXO22	GRCh38.p7	15:75917174	TTAGTGACCTAAACT[A/G/T]TAGTTATCTAGTTTT	26263
rs76586437	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924645	AAACCTTCATGTAAT[C/T]CAGGGAAGGGGCTCT	26263
rs76636379	snp	A/C	0.0138799	0.0821421	intron-variant	FBXO22	GRCh38.p7	15:75905724	TGCTTGATTTTTCCC[A/C]ATCTTGACACTTAGG	26263
rs76721113	snp	C/T	0.0174175	0.0916809	intron-variant	FBXO22	GRCh38.p7	15:75919641	GACTTTCATAAAACG[C/T]TTAGCAACAGTAGAT	26263
rs77063956	snp	A/G	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75905321	AACTTCTGATCCTGT[A/G]CTCTTTTGCTTCTCT	26263
rs77140102	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75925423	TTTTGAACCTTTAAC[G/T]ACTTGTCTTGAATTC	26263
rs77164215	snp	A/G	0.00358779	0.0422022	intron-variant	FBXO22	GRCh38.p7	15:75907793	TATTAAAGTACAAAA[A/G]TTGGCTGGGCATGTT	26263
rs77290423	snp	A/T	0.067446	0.170804	intron-variant	FBXO22	GRCh38.p7	15:75927274	GTCCTGAGATTTTTT[A/T]AAAATTTTCCTTTAC	26263
rs77975302	snp	A/G	0.00597247	0.0543191	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934297	AGAAGAAAAACAACA[A/G]AAGGATCCTGGTCCC	26263
rs78022571	snp	A/G	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75918589	GTTCACAATAGCTAG[A/G]ATATGGAATTAACCT	26263
rs78060086	snp	A/T	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75923126	CATCCTGGGAATCTT[A/T]GATGAGGCCCTGATA	26263
rs78449597	snp	A/G	0.00835141	0.0640778	intron-variant	FBXO22	GRCh38.p7	15:75918021	TTAATATAGTAAACA[A/G]CAAACGAATTACTCA	26263
rs78450543	snp	A/T	0.0023933	0.0345097	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902715	GATTTAATTTTTAAT[A/T]TGGTAAATATTGATA	26263
rs78531351	snp	C/G	0.02016	0.0983543	intron-variant	FBXO22	GRCh38.p7	15:75906089	GCTCAAATTACCCCT[C/G]TCACCCCCTAGTTTG	26263
rs78547036	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75931566	GTTTTACTACTAGCT[A/C]GCCTTATTACTTTAG	26263
rs78630828	snp	C/G	0.0103295	0.0711199	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903905	CCGGGCAACCCTATG[C/G]TGGCGTAATCGGGTT	26263
rs78653469	snp	A/G	0.0279526	0.114869	intron-variant	FBXO22	GRCh38.p7	15:75922879	GTTTTGATCCTAGGA[A/G]ACAAGGGTGATGGTG	26263
rs78767023	snp	C/G	0.0418186	0.138422	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903712	CCGCGCCACTCCACT[C/G]CCGCCTGGCCACAGC	26263
rs78909156	snp	A/G	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75907331	AATAATGAAAAGGTA[A/G]TGCATATAAACATTA	26263
rs79006436	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933918	GAATAGTTGGTATGT[C/T]AGCTAGTCATTCCTG	26263
rs79022260	snp	A/G	0.00676609	0.0577691	intron-variant	FBXO22	GRCh38.p7	15:75907426	TATTAAAGTTCACAT[A/G]GTTATAGTAATGCCC	26263
rs79483876	snp	C/T	0.0414363	0.137845	intron-variant	FBXO22	GRCh38.p7	15:75927260	TAAGGAGTTTGGAGG[C/T]CCTGAGATTTTTTTA	26263
rs79757311	snp	C/T			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930904	AAGTCATCCTAGTTA[C/T]AGTCTCTCTTCTGGT	26263
rs80197160	snp	C/T	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75906851	GTTTATAATAAGGGA[C/T]ACTAAAAACCTAATG	26263
rs80330090	snp	C/G	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75919341	ACAAAAATGGTAACT[C/G]TGAGATAATGCATAT	26263
rs111475770	snp	C/T	0.0414363	0.137845	intron-variant	FBXO22	GRCh38.p7	15:75912452	CAATTTCAGAACTTG[C/T]TATTGGTCTATTCAG	26263
rs111497654	snp	A/G	0.0360663	0.129354	intron-variant	FBXO22	GRCh38.p7	15:75920348	CCTGGCAGTCTGCCT[A/G]TAAAAGCATCAAGTG	26263
rs111499502	snp	A/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75909293	AGGTTTTGGAGAGGA[A/G]GTGGCACTTAAGGTG	26263
rs111633505	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934787	GCAAATATTTTTTAA[A/G]CTTTATTGTCCCTGA	26263
rs111749474	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75911512	TTCTTAGGTATTTTA[C/T]TCTCTTAGTAGCAAT	26263
rs111790547	in-del	-/ATATC	0.0414363	0.137845	intron-variant	FBXO22	GRCh38.p7	15:75907756	TATAAATATTTAAAA[-/ATATC]AAATATATAAATAAA	26263
rs111945324	snp	C/G	0.0414363	0.137845	intron-variant	FBXO22	GRCh38.p7	15:75911945	TACGTTCCATCAATA[C/G]CTAGTTTATTGAGAG	26263
rs112210662	snp	A/G	0.0178098	0.0926698	intron-variant	FBXO22	GRCh38.p7	15:75913700	GGGTATCCAAGATGC[A/G]CACACTCAGGTCCCA	26263
rs112276452	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931998	GCAGGAGGATTGCTT[C/G]AGCCCAGGAGTTTGA	26263
rs112804636	snp	A/C/T	3.29745e-05	0.00406031	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914149	CAGCACTTGCCCTTG[A/C/T]GAAGCTATTCCCCAA	26263
rs112978347	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921652	GGCGACAGCGAGACT[C/G]TATCTCAAAAAAATA	26263
rs113083073	snp	C/T	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75929302	CATAGCGAGACCCCA[C/T]CTCTACCAAAAAAAA	26263
rs113146835	snp	A/G	0.5	0	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933066	TCATAGCTATACAAC[A/G]ATAATGGCACTCATA	26263
rs113203125	snp	G/T	0.0111196	0.0737302	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903243	GAATAAAGGCAGTGA[G/T]TTTCACACACTAAGA	26263
rs113303781	snp	A/G	0.0414363	0.137845	intron-variant	FBXO22	GRCh38.p7	15:75910209	TCTTTGCTATTGTGA[A/G]TAGTGCTGCAGTAAA	26263
rs113399117	snp	C/T	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75928546	ATGAGAATACATCGA[C/T]GCAAAGAGGGGCACA	26263
rs113512124	snp	C/T	0.5	0	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933813	TATACCAATAAAACA[C/T]AGCGTGGAACTCATT	26263
rs113538816	snp	G/T	0.5	0	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903495	GAGCGGTGGCTTATG[G/T]CTGTAATTCCAGCAC	26263
rs113692448	snp	C/G/T	0.5	0	intron-variant	FBXO22	GRCh38.p7	15:75926654	GGTTGAGGGCGTATC[C/G/T]GGGAAAAACACTAGT	26263
rs113695642	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75916058	AGACTCTGTCTCCAA[A/G]AAAAAAAAAAAAAAA	26263
rs113911592	snp	C/G/T	0.021391	0.101607	intron-variant	FBXO22	GRCh38.p7	15:75904847	TTTTTTTTTTGAGAC[C/G/T]TAGTCTCGCTCTGTG	26263
rs114253696	snp	A/G	0.0193772	0.0965046	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902167	GTATGAACGGCATGC[A/G]CAGACTGGAGTTCCA	26263
rs114362346	snp	C/T	0.00853038	0.0647489	intron-variant	FBXO22	GRCh38.p7	15:75904650	TAGCAAGGGGTGTCA[C/T]GCACAGTCATTTGCA	26263
rs114544899	snp	C/G	0.0178098	0.0926698	intron-variant	FBXO22	GRCh38.p7	15:75915382	ACAGTGAGGTAAAAA[C/G]AATTTTACATGTTTA	26263
rs114667891	snp	A/T	0.0126979	0.078662	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933178	ACTTGGGCCATGTGT[A/T]TTTCAAACAAAAATA	26263
rs114894683	snp	C/T	0.0107246	0.0724382	intron-variant	FBXO22	GRCh38.p7	15:75904792	ACGGTAAGGATGTGT[C/T]ATGATTTATTTGACC	26263
rs115062753	snp	C/T	0.00557542	0.0525036	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931197	GATACCTCACTCAGA[C/T]TTATAACATCTGAGG	26263
rs115101510	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930801	CTTGTAAACACTACT[A/G]TTTGTTTCCCACTCT	26263
rs115167722	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75929309	AGACCCCATCTCTAC[A/C]AAAAAAAAAAAAATT	26263
rs115213056	snp	C/T	0.0217236	0.101931	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933394	TGACCTTAAATAGTC[C/T]TCCTGCATAGGAAGA	26263
rs115254038	snp	A/G	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75912072	ATATGTTTATATGAC[A/G]TGTATTGATTTGCAT	26263
rs115407087	snp	A/G	0.0611083	0.163768	intron-variant	FBXO22	GRCh38.p7	15:75915391	TAAAAAGAATTTTAC[A/G]TGTTTACAAATGAAT	26263
rs115818888	snp	A/G	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75919044	CTCACTGCTACTTCT[A/G]CTTCCTGGGTTCAAG	26263
rs115828439	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927108	TTTGCCTTTCCTGGT[C/T]GGGGGGAGGGGTGTG	26263
rs116259111	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934354	TAAGTGGCGTGGACT[A/G]TCTACCTCCAGACTG	26263
rs116366137	snp	A/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75916417	TCTCACTGTGTTCTC[A/C]TGTGGCCTTTTCTTC	26263
rs116604365	snp	C/G	0.0126979	0.078662	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902220	ACATGCTGCTTCATA[C/G]ATCCATGTTCGTAAG	26263
rs116749451	snp	C/T	0.00874735	0.0655527	intron-variant	FBXO22	GRCh38.p7	15:75931528	GAGGACTTCAGAAGA[C/T]GGATTTTGCCCCTCA	26263
rs117091386	snp	A/G	0.0158469	0.0875917	intron-variant	FBXO22	GRCh38.p7	15:75926604	ATGTGTGACTGAGGC[A/G]AGAATCTCCATCATT	26263
rs117323655	snp	A/G	0.0107246	0.0724382	intron-variant	FBXO22	GRCh38.p7	15:75927996	GCCAACAATCATAGG[A/G]AAAAAAGCTCCACAT	26263
rs117392811	snp	G/T	0.0107246	0.0724382	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930937	TCTCTATGAGCTAGA[G/T]CTGGGAAAATAGCTA	26263
rs117498241	snp	A/G	0.00358779	0.0422022	intron-variant	FBXO22	GRCh38.p7	15:75919828	CATGTGTCTGGGCTT[A/G]AAGTGACAATTAACG	26263
rs117526486	snp	C/T	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75915028	GTTGGAGTGCAATGG[C/T]GTGATCTCTACTCAC	26263
rs117674976	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75919888	CCAGATACTGTGCTG[C/T]GCAGCACTTCTAATC	26263
rs117729312	snp	A/C	0.0314385	0.121371	intron-variant	FBXO22	GRCh38.p7	15:75921184	AACATTAAAAAGGTA[A/C]AGTAAAAACATGGTA	26263
rs118004999	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75917581	TACATGTTTGGTAGA[A/G]TTGATTTACTTTTTA	26263
rs118060355	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75925474	AAAATAGAACTTTAA[G/T]GACTTGTCAGATTCC	26263
rs137901254	snp	A/G	0.0182019	0.0936463	intron-variant	FBXO22	GRCh38.p7	15:75921954	CTCCTTCTGGAATAC[A/G]TCCTGAAGGACCTGC	26263
rs137946219	snp	C/T	4.95086e-05	0.00497512	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917235	TTTTCTCTAGTGACT[C/T]CAATGGGATCAGGTA	26263
rs137973541	snp	C/G/T	0.000195642	0.00988883	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903994	TGCTGCGGCGAGTGC[C/G/T]GCGGCTCCTCCGTAG	26263
rs138410482	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920235	CAGCAAACTAGGTCT[C/T]TTTCAGAGTTGGTCA	26263
rs138491368	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75928421	AAAAGAATGAGATCA[C/T]GTCCTTTGCAGGGAC	26263
rs138543078	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934955	AGTCTGATACAGGGT[A/G]ATTTCATACAATATT	26263
rs138588233	snp	A/C	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75929212	CTTTGTACATCTTTC[A/C]TTATGAGGACACTGT	26263
rs138635967	snp	G/T	1.64732e-05	0.0028699	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904539	AGTATTGCGGACCCA[G/T]CGGAGCGTAACCTGG	26263
rs138944943	snp	G/T	0.00755907	0.0610114	intron-variant	FBXO22	GRCh38.p7	15:75914692	GTTTTTATTATTTTT[G/T]ATTCTTTTCTGTAGT	26263
rs139127277	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930657	AATATTTGCTCTTCT[C/G]TCTTGGGAGCCATTA	26263
rs139199045	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915059	TGCGACTTCTGCCTC[A/C]TGGATTCAAGCAATT	26263
rs139399078	snp	A/G	0.000263531	0.0114759	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932928	GGCTGATGCATTTAG[A/G]AAGTTTTTTCCTAGT	26263
rs139430756	in-del	-/C	0.0158469	0.0875917	intron-variant	FBXO22	GRCh38.p7	15:75928676	AATCTGCACAACAAA[-/C]CCCCATGACACACGT	26263
rs139502637	snp	C/T	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75906035	ACTCTCGGAGTCTTA[C/T]TTAATTCAGTGGGAT	26263
rs139841300	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75926711	AGAGGTTTTCAATAC[A/G]TGTTTTTAAAGGAGA	26263
rs139868423	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923273	ATAGTGCCAAGTATA[C/G]GAATGAGAAAACTGG	26263
rs140199998	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75905560	ATCACTGATACATTT[C/G]TACCATTTTATCCTC	26263
rs140383856	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902763	CTATTGGTCGTGTCA[A/G]TATTTTAGGGTGTAA	26263
rs140491531	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75919143	CTGGCTAATTTTTTT[-/T]GTCTTTTTATTAGAG	26263
rs140537639	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934159	GAATGTGAGGGGAAA[C/T]GATTTTTTGTGTCCT	26263
rs140556036	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75904845	TTTTTTTTTTTGAGA[-/C]CGTAGTCTCGCTCTG	26263
rs140618264	snp	A/C	0.00199481	0.0315187	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932520	ATTTTTTATGTATTA[A/C]TTTTGATTTTTGACC	26263
rs140801163	in-del	-/G			intron-variant	FBXO22	GRCh38.p7	15:75925779	AGGGGAGAGAGATCA[-/G]GCTCAACTCCAAATG	26263
rs140841328	snp	C/T	9.9557e-05	0.00705468	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904076	TGCTCACCTTCCTGC[C/T]CGCCAAGGCGTTGCT	26263
rs140854350	in-del	-/GGG	0.0256215	0.110247	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932281	TTGACAGCTGAAGTC[-/GGG]GGGAAGAGATGTTAA	26263
rs140893622	snp	A/G	0.000153988	0.00877327	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932782	AACGAGGACGTCAGT[A/G]ATGAGAAGACTGCTG	26263
rs141159167	snp	A/G/T	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75907858	TGAGGTACCAGAATC[A/G/T]CTTGAACCAGGGAGA	26263
rs141220458	snp	A/G/T	8.23752e-05	0.00641732	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932990	AAATTGGATGTGATC[A/G/T]GATAGTCACTGGGAA	26263
rs141297207	snp	A/C	0.000155988	0.00883005	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903971	GGTGAGGAATGGAGC[A/C]GGTAGGCTGCTGCGG	26263
rs141471437	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934423	GTATGATGTAACTAA[C/T]GTTACTTTTGTAACA	26263
rs141629665	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919771	ATAGTAGGGTTCTAA[A/G]TGTCCTTAGCTCATT	26263
rs141694406	snp	C/T	0.00636936	0.0560724	intron-variant	FBXO22	GRCh38.p7	15:75912918	GTGCTATAAATTTCC[C/T]TGTAAACACTGCTTT	26263
rs141884496	snp	A/G	0.00835141	0.0640778	intron-variant	FBXO22	GRCh38.p7	15:75908677	GGTAGCTCAATAGTC[A/G]TAGCACCATGGCAGT	26263
rs141910904	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903300	TATAAATCGAGCTTA[C/T]GCTATTTAAACAGGC	26263
rs142303922	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75928771	ATAAACAAGCTGCCA[A/G]AGGCTCCAGTGAAAC	26263
rs142372170	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922139	GCTATACTTTTATAC[A/G]ACTGGCACTGCAATA	26263
rs142413858	snp	A/G	3.29478e-05	0.00405867	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932797	GATGAGAAGACTGCT[A/G]AGGCTGCGATGCAGC	26263
rs142478614	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926892	GGGTGAATTACTGAT[C/G]TCTTGTTTTTGTGCA	26263
rs142488860	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920466	GAAGAAGATGATCAA[C/T]GTGTTGATGTTGACG	26263
rs142724325	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926612	CTGAGGCGAGAATCT[C/T]CATCATTCGAGGTTT	26263
rs142845079	in-del	-/CTTT	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75924901	CAAATATCCTTCTGA[-/CTTT]CTTCTAGGTGAAGCA	26263
rs143130005	snp	A/C/T	0.00319074	0.0398324	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902319	CGCCTGTTTATCTTC[A/C/T]TCTGGTATTCCGCAA	26263
rs143168422	snp	A/G	0.00478085	0.0486577	intron-variant	FBXO22	GRCh38.p7	15:75909815	ATACATGTGCAGAAC[A/G]TGCAGGTTTGTTACA	26263
rs143192799	in-del	-/TACAG	0.0418186	0.138422	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931160	AATGGTGATTCAACA[-/TACAG]TTTACCTTTGAAATG	26263
rs143240378	snp	C/G	0.0134861	0.0810011	intron-variant	FBXO22	GRCh38.p7	15:75912575	GGTGTTTATGGTATT[C/G]TCTGATGGTAGTCTG	26263
rs143346313	snp	C/T	0.0150606	0.0854603	intron-variant	FBXO22	GRCh38.p7	15:75921212	GTATGAAAGACAGTA[C/T]ACCTCTATAGGGCAC	26263
rs143480986	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929999	CAGTGATATGAATAT[C/T]ATCTTGGCTGGAGGC	26263
rs143665207	snp	A/T	0.000153988	0.00877327	stop-lost, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933102	GGGGTCATCTAAATA[A/T]TAATTAAAGTGGCTT	26263
rs143863360	snp	G/T	0.0287284	0.116357	intron-variant	FBXO22	GRCh38.p7	15:75910714	CCCATTCTGTAGGTT[G/T]CCTGTTCACTCTGAT	26263
rs144006488	snp	A/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75913526	AAGGTGTTGTTCTCA[A/G]TTTGAGATGCTTTAA	26263
rs144060443	snp	C/T	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75915503	TGGCGTGGTGGCTGA[C/T]ACCTGTAATCCCAGC	26263
rs144125274	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75910523	CTAATGACTAGTAAT[A/G]ATGAGCTTCTTTTCG	26263
rs144326532	snp	A/T	0.0146672	0.084371	intron-variant	FBXO22	GRCh38.p7	15:75904701	AGAACTATTTTTTTT[A/T]AAATCCCAGTTTTGT	26263
rs144439090	snp	C/T	0.000153988	0.00877327	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913281	GAAGAGTGTCGTGGC[C/T]ATAAGAGAGGTAAAT	26263
rs144464691	snp	A/G	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75915047	ATCTCTACTCACTGC[A/G]ACTTCTGCCTCCTGG	26263
rs144572221	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926258	TGAATTGGGGGGAAC[C/G]CAGAACCTTTCAGGA	26263
rs144589375	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934804	TTTATTGTCCCTGAT[A/G]TTAACCAGAATTGGT	26263
rs144610854	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929044	AACGAGAAATTTATT[C/T]TGCACAGTTCAGGAG	26263
rs145016468	snp	A/G	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75905588	CTCAGACTCGGTTCA[A/G]ATTTTGCCAGTTGTC	26263
rs145078162	snp	G/T	6.93217e-05	0.00588694	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903980	TGGAGCCGGTAGGCT[G/T]CTGCGGCGAGTGCCG	26263
rs145351222	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926821	CACTTTACATAAGAT[A/G]AGGTGAACCTTTTGA	26263
rs145456922	snp	G/T	0.00835141	0.0640778	intron-variant	FBXO22	GRCh38.p7	15:75906916	TGCAAATGCATTAAT[G/T]ACAAGAGAAAATGTT	26263
rs145521253	snp	A/T	0.00438332	0.0466095	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903041	GATAAGGACCGGGAA[A/T]GTGCTAAAACTTAGT	26263
rs145638487	snp	C/T	0.00835141	0.0640778	intron-variant	FBXO22	GRCh38.p7	15:75908335	TGGATTGCAGTGGCC[C/T]GATCTTGGCTCAGTG	26263
rs145642230	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75912516	GGGGTATGTGTCCAG[G/T]AATTTATCCATTTCT	26263
rs145644601	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903898	GCGCCGGCCGGGCAA[C/T]CCTATGCTGGCGTAA	26263
rs145722802	snp	G/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75919691	TGGCCTCCACCCTAG[G/T]CAGGCTTTACTGTGT	26263
rs145961451	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922702	TGTCATCGAGCAGAG[C/G]TGAATGTGGCCCTCC	26263
rs145995053	snp	A/G	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75915541	GAGGCCGAGGCAGGC[A/G]GATCACTTGAAGTCA	26263
rs146575958	in-del	-/C	0.0418186	0.138422	intron-variant	FBXO22	GRCh38.p7	15:75913790	ATAGTAGTTATACTG[-/C]CAATATCAGCTGAAC	26263
rs146624641	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934317	ATCCTGGTCCCTGTA[C/T]GACCTCATTGAAGAA	26263
rs147053273	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920209	GTAGGCTAGCTGGAG[C/T]GAACAAAGTTCAGCA	26263
rs147082526	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75912936	TAAACACTGCTTTAG[A/C]TGTGTCCCAGAGATT	26263
rs147206411	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932512	CCTTGTGCATTTTTT[A/G]TGTATTAATTTTGAT	26263
rs147523828	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75905243	CGGGAAGACAACTGG[A/G]TGTGTCTTGCTCAGT	26263
rs147572184	in-del	-/ATAA	0.021333	0.101051	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902393	TAAGCAGCTGCGCCT[-/ATAA]ATAGACTATGGGAAA	26263
rs147574665	snp	A/C	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75905985	AAACTATGTAAATAT[A/C]GTGTTTCAATTCATT	26263
rs147577770	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901979	GTCACTGGTAAACTG[G/T]CCTCTTTCCCTACTT	26263
rs147680022	snp	G/T	0.0154538	0.0865337	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932626	TCAGGAGGATTTTGC[G/T]TCTATACTTAAAAAT	26263
rs147682596	snp	C/T	0.00438332	0.0466095	intron-variant	FBXO22	GRCh38.p7	15:75926876	ATGTCTCAGAGTAGG[C/T]GGGTGAATTACTGAT	26263
rs148094403	snp	A/C	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75908667	AAGAGGGTCAGGTAG[A/C]TCAATAGTCGTAGCA	26263
rs148322195	snp	A/C	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75912813	TTCTGCTAGCTTTTG[A/C]ATTTGTTTGCTCTTG	26263
rs148602140	snp	G/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75911210	CATGATGCCTCCAGC[G/T]TTTTTCTTTTTGGTT	26263
rs148738256	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933816	ACCAATAAAACATAG[C/T]GTGGAACTCATTCAG	26263
rs148779868	snp	G/T	0.0146672	0.084371	intron-variant	FBXO22	GRCh38.p7	15:75904747	CTCGTTCCGTGAAAA[G/T]ATTTTGTAAACATCA	26263
rs148792228	in-del	-/GGGC	0.0178098	0.0926698	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903107	CTGGTGCACAGCTTG[-/GGGC]GTGCTTCACAGCAAT	26263
rs148868806	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75906686	CTGGAACTCTCATTC[C/T]AGGGAGCTGGCCAGT	26263
rs149003125	snp	C/G	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75928190	GTGGAAGATAGTGTG[C/G]TGATTCCTCAAAGAC	26263
rs149069906	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902175	GGCATGCACAGACTG[C/G]AGTTCCAGACAAGCA	26263
rs149131227	snp	G/T	0.0111196	0.0737302	intron-variant	FBXO22	GRCh38.p7	15:75912539	CCATTTCTTCTAGAT[G/T]TTCTAGTTTATTTGC	26263
rs149234743	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914946	TAGAGATACACAAAG[C/T]AGTAAGTAAATGTTA	26263
rs149248344	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935634	CAATCTAGTAGGCCA[A/G]TTCACATTACAGTTA	26263
rs149330812	snp	C/T	0.00453482	0.0474009	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75913225	GCATCTTACCACATA[C/T]AGTTCTTTACATGGC	26263
rs149528792	in-del	-/A	0.0718919	0.175435	intron-variant	FBXO22	GRCh38.p7	15:75928730	TGTATCCCTGAACTT[-/A]AAAAAAAAAATCAAA	26263
rs149601564	snp	G/T	0.0107246	0.0724382	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903906	CGGGCAACCCTATGC[G/T]GGCGTAATCGGGTTC	26263
rs149770482	snp	A/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75917798	AAGTTTTTAGAATAC[A/G]CGGGTTAGTTCTTTG	26263
rs150074021	snp	C/T	0.000153988	0.00877327	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932950	TTTCCTAGTGTTCCC[C/T]TATTCGGCTTCTTTG	26263
rs150157752	snp	C/T	0.000230605	0.0107354	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904537	AGAGTATTGCGGACC[C/T]ATCGGAGCGTAACCT	26263
rs150210484	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909121	TCCTTTTCATTTAAT[G/T]CAGCTGCTTTGCCGC	26263
rs150244660	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927620	ATATATTCTCTTAAA[A/G]TTTCGTGGGCTAGTC	26263
rs150417055	in-del	-/TT	0.0209421	0.100162	intron-variant	FBXO22	GRCh38.p7	15:75908440	GCCATACCCGGTTAC[-/TT]TTTGTATTTTTAGTA	26263
rs150457602	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934245	GATCTGGTAGTGAGC[C/T]ATCTTGGACCCTGAA	26263
rs150685027	snp	G/T	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75914663	GCTTGATTGCTGCTG[G/T]TGAATTTTTGCTGGT	26263
rs150713293	snp	C/T	0.00755907	0.0610114	intron-variant	FBXO22	GRCh38.p7	15:75921805	TTAAAAACTAAAACA[C/T]AGTCACACACATTAG	26263
rs150766833	snp	C/T	0.0460142	0.144533	intron-variant	FBXO22	GRCh38.p7	15:75929529	GTTTTTTTTTTTTTG[C/T]TCCCTACTGAGAGCC	26263
rs150887253	snp	A/C/G	0.00047764	0.0154469	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932823	GCAGCGCCTCAAAGC[A/C/G]GCCAACATTCCAGAG	26263
rs151202217	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902493	GTCTTGAGGCCAGGA[A/G]TTTGAGACCAGCCTG	26263
rs151278464	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934103	AATAAAGACTACATT[A/T]CCCAGTCTCCTGTGC	26263
rs180694717	snp	A/G	0	0	intron-variant	FBXO22	GRCh38.p7	15:75913950	AGCCAGGACCAAAAC[A/G]GGTAAAGTGTTTGTT	26263
rs180831394	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925204	TAATATGGATATAAT[A/T]TGCATGTTAAATGTG	26263
rs180852836	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906228	GGTTTTACCTGCCTT[C/G]GTCCTGGAATTGGCC	26263
rs180938043	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75910086	CCATGTCCCTGCAAA[A/G]GACATGAGTGCATCC	26263
rs180957319	snp	A/G			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930859	ACATGGGGACAGACT[A/G]TTGCAGATCAGTATC	26263
rs181291536	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75919749	GGCCTTGTAGTTTGT[A/G]GGGGGAATAGTAGGG	26263
rs181299040	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902153	GAGGGGCGGGGGAGG[C/T]ATGAACGGCATGCAC	26263
rs181406397	snp	A/G	0.00438332	0.0466095	intron-variant	FBXO22	GRCh38.p7	15:75929584	GTTGCTGCTCAGTAC[A/G]TAGCTGCTTCATTAT	26263
rs181540861	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909618	TCATTATGAAAATGA[A/C]CTTTTTGAGGGCTGG	26263
rs181590779	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923482	TAATTTTAGGTAGAG[C/T]TGGCCTTCCATATCC	26263
rs181602173	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905961	ATTGTTTTGTGAAGA[A/G]ATCATTTGAAACTAT	26263
rs181609401	snp	C/T	0.00636936	0.0560724	intron-variant	FBXO22	GRCh38.p7	15:75919557	ATTTTTCTAAACCTC[C/T]ATTTTCCTCATCTAT	26263
rs182020465	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75914640	CATGAGGTTGTGCCC[C/T]TTTCCATGCTTGATT	26263
rs182179245	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916251	CAATTTTCTGTAGAC[C/T]TGTAACCTACTGTGT	26263
rs182228924	snp	A/G	0.0107246	0.0724382	intron-variant	FBXO22	GRCh38.p7	15:75911451	TCCTTGAGCAGTGGT[A/G]TGTAGTACTCCTTGA	26263
rs182241233	snp	G/T	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75921530	TAGCTGGGCATAGTG[G/T]TGTGCGCCTGTAGTC	26263
rs182263467	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922740	GGAGACACTGGAAGC[A/G]GGAGACCACTTTAGA	26263
rs182535910	snp	A/G	0.00636936	0.0560724	intron-variant	FBXO22	GRCh38.p7	15:75908509	CCCTGGCCTCAGGCA[A/G]TCCACCCACCGTGGC	26263
rs182559244	snp	G/T	0.00755907	0.0610114	intron-variant	FBXO22	GRCh38.p7	15:75904954	TCAGCCTCCCGAGTA[G/T]CTGGGACTACAGGCG	26263
rs182774816	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927225	TGACTCAGCCTCTAG[G/T]CTAAACTTTCCCTTT	26263
rs182859526	snp	A/G	0.00874735	0.0655527	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932281	TTGACAGCTGAAGTC[A/G]GGGGGAAGAGATGTT	26263
rs182875558	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933430	AGGGTATTCATCAAT[A/G]GGATATAGATTTAAG	26263
rs182904437	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902396	GCAGCTGCGCCTATA[A/G]ATAGACTATGGGAAA	26263
rs183022417	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75910829	TGTTTTAGTCATGAA[A/G]TCTTTGCCCATGCCT	26263
rs183027114	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931409	ATAACCCAACTGACC[C/G]AGTGCCCCAAAAGGA	26263
rs183065172	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926756	GAAGGATAGGCATGA[A/G]GTGAATGGTTACATT	26263
rs183071841	snp	C/T	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75908164	CTCAGGACCAGACTT[C/T]TAATACTTGTTCAGG	26263
rs183146917	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75916384	GATGGTCTCTCTGAA[A/G]CTTACTTACAGCTGC	26263
rs183380747	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911348	GAATCTCTAAATTAC[C/T]TTGGGCAATATGGGC	26263
rs183407713	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902757	CATAAACTATTGGTC[C/G]TGTCAATATTTTAGG	26263
rs183494580	snp	C/T	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75915216	CCTCAGGTGATCCAC[C/T]GCCTCAGCCTCCCAA	26263
rs183617071	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921969	GTCCTGAAGGACCTG[A/C]CTGAGGCTGTTTTAC	26263
rs183717316	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918170	TAGATCAGCCAGCCT[A/G]TAGAGATAAACCTCT	26263
rs183994056	snp	C/T	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75926107	TGCCTTATAAATACT[C/T]TTCTGGAATTGTTTT	26263
rs184042146	snp	A/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75922456	ATTTAAGCCCTTGAA[A/G]GATGGGAAGCATATG	26263
rs184057589	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903586	CCGTCTCTACAAAAA[A/G]TACAAAAATTAGCTG	26263
rs184164566	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906664	TTCTCCTTACCTTGT[C/T]TGGGCTCTGGAACTC	26263
rs184274986	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934295	GTAGAAGAAAAACAA[C/T]AGAAGGATCCTGGTC	26263
rs184282266	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75912059	GTTTATATGATGTAT[A/G]TGTTTATATGACGTG	26263
rs184359567	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922591	CAAAGGTTATGTGCA[A/G]GGAAGTCATGGGAAC	26263
rs184484569	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904794	GGTAAGGATGTGTCA[C/T]GATTTATTTGACCGT	26263
rs184509585	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75909146	TGCCGCTTGTCTTCA[A/G]TTGGAAAGTTTAGTT	26263
rs184511307	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929087	AAATTGAGATGGCAG[G/T]AGGGGTAGTGCTACC	26263
rs184771169	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918929	GTCTGTTGTACAACA[C/T]GGAGACTATAGTCAG	26263
rs184983827	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902303	AAAGGTAACTGGAGG[A/G]CGCCTGTTTATCTTC	26263
rs185097565	snp	C/T	0.00835141	0.0640778	intron-variant	FBXO22	GRCh38.p7	15:75905178	CAACGCTGTGCAGAA[C/T]CTTCCCTTCACCTGC	26263
rs185190138	snp	C/G	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75916720	TTTAATGGCTATATT[C/G]TATGATACCAATGTA	26263
rs185200420	snp	A/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75922978	CAAACCCCATTAGAG[A/T]TGCTTGTTTTGGCTG	26263
rs185318903	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923979	GTCATGCGGGTATGT[A/G]GCTAGCGCAGCTGTA	26263
rs185324971	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905998	ATCGTGTTTCAATTC[A/G]TTTATTTATTTATAT	26263
rs185421282	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927648	GTCTATAAGGGAAAA[A/T]AGATGCTTTAGCAAT	26263
rs185490469	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75914266	GGGGTCCTTTGGATT[A/G]GTGAGTTATTTTTAG	26263
rs185559104	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75919776	AGGGTTCTAAGTGTC[C/G]TTAGCTCATTCAGAA	26263
rs185564976	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908853	TTTTCTGAAAATGCT[G/T]TGTGGACCAAGGAAA	26263
rs185866395	snp	C/T	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75909752	AAGAAGGTAGGGTAC[C/T]AGCAGTTTGGATGGG	26263
rs185986999	snp	A/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930245	TAATTACATTTTTAT[A/T]TATATTGTCCTTCAA	26263
rs185995931	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914785	GAATGCCGGCTGTAC[C/T]GCTTAGTATCTGTAT	26263
rs186108743	snp	A/G	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75925638	CCTTCGAAGTTGCCC[A/G]GCCCTTGAGAAAGCA	26263
rs186243718	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75910897	TTTTTATGGTTTTAG[C/G]TCTTACATTTAAGTC	26263
rs186257054	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75906446	AATTATATTTCTATA[C/T]ATATGTGGAGGCTCA	26263
rs186311041	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910453	TGACCTTTTAATGAT[C/T]GCCACTCTAACTGGC	26263
rs186335937	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915762	AAAATTAGCCAGGCA[A/T]GATGGCGGGCACCTG	26263
rs186777174	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916367	AGAAGTCCAAGATCG[G/T]GGATGGTCTCTCTGA	26263
rs186946594	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75919685	TAGTGTTGGCCTCCA[C/T]CCTAGGCAGGCTTTA	26263
rs186989629	snp	A/G	0.00993419	0.0697739	intron-variant	FBXO22	GRCh38.p7	15:75908272	TCTGTTTTTTGTTTT[A/G]TTTGGTTTTTTTTTT	26263
rs186989744	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75927109	TTGCCTTTCCTGGTC[A/G]GGGGGAGGGGTGTGA	26263
rs187011530	snp	A/G			downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931293	CCCACCCCAATCATT[A/G]CTCTTCACATGACCC	26263
rs187233518	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75922510	CTGGCTGAAGGAACA[C/T]AGAAACACAGGCACA	26263
rs187236887	snp	C/G	6.61616e-05	0.00575121	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904027	CCGCGGAGCACCTTC[C/G]TGTTGAGTAACCTGG	26263
rs187501194	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926463	GTTCTTTAAGTTGGG[G/T]TAGGGGAAAGTGATT	26263
rs187694850	snp	A/C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927512	GGGTAGTAGTCACTT[A/C/T]TCTGGCATTGGCAGT	26263
rs187752275	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911502	GTAAGTTGTATTCTT[A/C]GGTATTTTATTCTCT	26263
rs187756698	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933701	TTATTATAAGTAAAA[G/T]ATTTTTCTTCTTTCC	26263
rs187982805	snp	A/C	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75907149	TATACATTGTAGTGG[A/C]TGTTAATAGCCAGAC	26263
rs188003556	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908733	CTTAGTTAAGAGGCA[C/T]GTAGTCTAAGTGTTG	26263
rs188066432	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911353	TCTAAATTACTTTGG[C/G]CAATATGGGCATTTT	26263
rs188243514	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917526	CCTGTCACTGGAGAT[A/G]TGGCTAATTCAAACA	26263
rs188325115	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932645	ATACTTAAAAATTTT[A/G]ATGTTTCATGAGATA	26263
rs188383081	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75918578	ATTGCAGCACTGTTC[A/C]CAATAGCTAGGATAT	26263
rs188505990	snp	A/T	0.00438332	0.0466095	intron-variant	FBXO22	GRCh38.p7	15:75922312	CTTGACCAAAGTGTT[A/T]TGTGGTGCTTGACTG	26263
rs188516568	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929385	CAGAGGTTTGATGTG[C/G]ATATACCTTTGGCAT	26263
rs188518597	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909151	CTTGTCTTCAATTGG[A/C]AAGTTTAGTTGAAAA	26263
rs188597865	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902534	ACCCTGGGTCTACCA[A/G]AAAAAAGAAAAAAAC	26263
rs188797558	snp	G/T	0.00478085	0.0486577	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902916	AACCTGTGTCTGCTG[G/T]GCTTCCATTTCTTGG	26263
rs188851232	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916454	AAGCATGCTTGGTGT[C/T]TCTTCCTCCTCTTCT	26263
rs188878589	snp	C/T	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75921623	CCAAGATTACACCAC[C/T]GCACTCCAGCCTGGG	26263
rs189037798	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905228	TGTTGTCTGTTTTAC[C/T]GGGAAGACAACTGGG	26263
rs189041811	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934758	TCCTTGAATGTGCTC[A/G]TATAGCCCATAAGGC	26263
rs189048246	snp	A/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75912447	TGCCTCAATTTCAGA[A/C]CTTGTTATTGGTCTA	26263
rs189050631	snp	A/C/G	0	0	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930836	AATATTTGCATCCTA[A/C/G]AGTGGTGACATGGGG	26263
rs189354847	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75910051	GTTAGTTTGCTGAAA[A/G]TGATGGTTTCCAGCT	26263
rs189372059	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927949	GTCCCCAAAGCACCC[A/G]TTTGGTAATGCTGGC	26263
rs189376467	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908877	AAGGAAACTATATCC[A/G]TAGGTCTTGGGCAGC	26263
rs189421182	snp	C/T	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75914587	TTACTAGGAGACTTC[C/T]GTTTCTCTGCTTTGG	26263
rs189591440	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75921137	GGCAGTTGTAACACA[A/G]TGGTAAGTATTGGTG	26263
rs189597448	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902393	TAAGCAGCTGCGCCT[A/G]TAAATAGACTATGGG	26263
rs189879768	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923422	TTGAAGCTTTGCCCA[G/T]CTTAAAATGGCCATC	26263
rs190124049	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906026	TATCTGTACACTCTC[A/G]GAGTCTTATTTAATT	26263
rs190128043	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924299	AATATTATTTTGACA[C/T]CCCTCCCTTCTGCTA	26263
rs190164437	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932250	TATTATATTTTTAAT[A/G]TACATCTTTCAGAAT	26263
rs190419785	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919310	GCTAAGAGAGTGACT[A/G]TTAAGTGTTCTTACT	26263
rs190501265	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926685	CACAAACGAGTGGCT[C/G]TGTACTCTGAAGAGG	26263
rs190505745	snp	C/T	0.00557542	0.0525036	intron-variant	FBXO22	GRCh38.p7	15:75907661	AGCACTTTGGAAAGC[C/T]GAGGCAGGCAAATCA	26263
rs190619210	snp	C/T	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75922690	CTGTTACTCAGATGT[C/T]ATCGAGCAGAGGTGA	26263
rs190808867	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916371	GTCCAAGATCGGGGA[A/T]GGTCTCTCTGAAGCT	26263
rs191042884	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75910537	TGATGAGCTTCTTTT[C/T]GTATGTTTGTTGGCC	26263
rs191047025	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75931407	AGATAACCCAACTGA[C/G]CCAGTGCCCCAAAAG	26263
rs191106000	snp	C/T	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75911147	TTGGTACCAGTACCA[C/T]GCTGTTTTGGTTACT	26263
rs191188152	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915790	CTGTAATCCCAGCTG[C/T]TCAGGAGGCTAAGGC	26263
rs191258743	snp	G/T	0.000215273	0.0103726	intron-variant	FBXO22	GRCh38.p7	15:75904663	CATGCACAGTCATTT[G/T]CAGGTTGGTGGTTCA	26263
rs191262777	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75922546	AGGAAATCCCAGAGC[A/G]TGTTGGAGAAATAGT	26263
rs191364656	snp	A/C	0.00478085	0.0486577	intron-variant	FBXO22	GRCh38.p7	15:75919719	TGTGTCACATGGGCC[A/C]TTCATCTGCAGTGTG	26263
rs191693980	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922334	GCTTGACTGCATAAT[C/T]ATAACCCAAGTGAGT	26263
rs191704996	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903154	TACCTTAGAATGGCA[C/G]GTGCTATTTATGCCA	26263
rs191720357	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75914901	GGGTTGTGAGAATTA[A/C]ATGAGTTAACACTTG	26263
rs191902479	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75928765	TAGTCTATAAACAAG[C/T]TGCCAGAGGCTCCAG	26263
rs191911218	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75909021	TCCATTTAACTAACA[A/G]TGAGGCTTTGCTATA	26263
rs191922185	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75906568	GGGAAACCTGGTTCT[C/T]ATCATTCTTAATGTA	26263
rs191932514	snp	A/G	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75927128	GGAGGGGTGTGAGGC[A/G]GTAGGTCTGGCTAAT	26263
rs191934539	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75908418	GTTGGGACTACAGGC[A/G]CATGCAGCCATACCC	26263
rs192130613	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75921836	CCTAGGCCTATACAG[A/G]GTCAAGATAATATCA	26263
rs192172561	snp	A/G	3.29457e-05	0.00405854	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932902	TATTACAGAGCCAAG[A/G]GGAATGTTGAGGCTG	26263
rs192212825	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75925697	AAAAAAAAAAGCGAT[G/T]CTGACATCTATTCAA	26263
rs192510415	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902750	TAACACACATAAACT[A/G]TTGGTCGTGTCAATA	26263
rs192585594	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75911392	CGATTCTTCCTATCC[C/T]TGAGCATGGAATGTT	26263
rs192669101	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911705	TACAATCATGTCATC[C/T]GCAAACAGAGACAAT	26263
rs192670602	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933835	GAACTCATTCAGGTA[A/G]TGTTTTGCATTTCAT	26263
rs192760281	snp	A/G	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75927605	GTTCTAAAGAAGAAA[A/G]TATATTCTCTTAAAA	26263
rs192781247	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918055	AAAGCAGCGTTTAGC[C/T]TTTTATCTACATCTG	26263
rs192952363	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75913081	TGTGTGGTTTTGAGT[A/G]AGTTTCTTAATCCTG	26263
rs193033973	snp	C/G	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75916595	TAAACATGAATTTGG[C/G]GTAGGCAGTAGGGAG	26263
rs193053247	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75908737	GTTAAGAGGCACGTA[C/G]TCTAAGTGTTGCCAA	26263
rs193173720	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935555	AAATCTAAGGAAGAG[C/G]GAAAGTAAACCTTGA	26263
rs199545616	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75921642	CTCCAGCCTGGGCGA[A/C]AGCGAGACTCTATCT	26263
rs199549004	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75911944	ATACGTTCCATCAAT[A/T]CCTAGTTTATTGAGA	26263
rs199590150	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75904729	TGTTAATTAAAGGAA[C/G]ATCTCGTTCCGTGAA	26263
rs199887271	snp	G/T	1.65715e-05	0.00287845	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913278	CTGGAAGAGTGTCGT[G/T]GCCATAAGAGAGGTA	26263
rs199916349	snp	A/G	4.97154e-05	0.0049855	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913276	GTCTGGAAGAGTGTC[A/G]TGGCCATAAGAGAGG	26263
rs199926302	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75925457	CAGCCACCAAGAGGG[G/T]TAAAATAGAACTTTA	26263
rs199940270	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75916864	TTTTTAGGGTAAACT[C/T]TTAAAAATTGGAATT	26263
rs200086646	snp	A/C/G	0.000132592	0.00814124	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932724	GGGTGTGGTTGGACT[A/C/G]TCATTTAGTGGACAC	26263
rs200155248	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75909790	TTTTTTTTTTTTTTA[A/T]ATTTCTGCGATACAT	26263
rs200200794	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75917582	ACATGTTTGGTAGAA[C/T]TGATTTACTTTTTAA	26263
rs200360759	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75911895	GTATGATACTGGCTG[G/T]GGGTTTGTCATAAAT	26263
rs200534672	in-del	-/A			intron-variant	FBXO22	GRCh38.p7	15:75911604	CTTGTGATTTCTGCA[-/A]CATTGATTTTGTATC	26263
rs200646126	snp	A/C	1.64738e-05	0.00286995	intron-variant	FBXO22	GRCh38.p7	15:75904447	CTGTGGGAGAGACGA[A/C]AATGAACGTCCGTTC	26263
rs200729232	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75904730	GTTAATTAAAGGAAC[A/T]TCTCGTTCCGTGAAA	26263
rs200730179	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75931993	CTGAGGCAGGAGGAT[C/T]GCTTGAGCCCAGGAG	26263
rs200975657	snp	A/C	9.89805e-05	0.00703423	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917258	ATCAGGTAGCAATCG[A/C]CCTCAGGAAATAGAA	26263
rs200990698	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923068	GTCCAGAGAGGTGAC[A/G]TAGCTGTTTCCTGGG	26263
rs201138132	snp	C/T	0.000164731	0.00907405	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932839	GCCAACATTCCAGAG[C/T]ATAACACCATTGGCT	26263
rs201240859	in-del	-/T	0.0142736	0.0832652	intron-variant	FBXO22	GRCh38.p7	15:75917786	CAAGCATTTTAGAAG[-/T]TTTTAGAATACGCGG	26263
rs201530123	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75911935	TATTTTGAGATACGT[C/T]CCATCAATACCTAGT	26263
rs201567790	snp	A/G	0.000399281	0.0141238	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904541	TATTGCGGACCCATC[A/G]GAGCGTAACCTGGAT	26263
rs201681565	snp	A/T	0.0349115	0.127424	intron-variant	FBXO22	GRCh38.p7	15:75929324	CAAAAAAAAAAAAAT[A/T]TTTTTTAAAGATCCT	26263
rs201772334	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75916863	ATTTTTAGGGTAAAC[A/T]TTTAAAAATTGGAAT	26263
rs202137178	snp	C/G	0.000237381	0.0108919	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932701	AACCCTCTGGATATT[C/G]ATGCCTCGGGTGTGG	26263
rs202138375	snp	A/G	0.000745027	0.0192862	intron-variant	FBXO22	GRCh38.p7	15:75917200	GTTTTTACTGACTCT[A/G]TTGGTGAAACTGTTT	26263
rs202204059	snp	C/T	0.000556057	0.0166649	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930136	TAACAATTTAAAAAA[C/T]GTGTTTAAAGAATTA	26263
rs267604328	snp	A/C			synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932973	CTTCTTTGGAAATGG[A/C]GAAATTGGATGTGAT	26263
rs367582662	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75911725	ACAGAGACAATTTGA[A/C]TTCCTCTCTTCCTAT	26263
rs367627596	in-del	-/T	0.00631501	0.0558357	intron-variant	FBXO22	GRCh38.p7	15:75913183	GGGATCCAATTCCAA[-/T]TTTTTTTTTTTCTTT	26263
rs367802766	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933313	AGGAGTTGAGAGCTT[C/T]TGCATCAGGCAGAAG	26263
rs367909006	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927688	TATATGATGTCATGA[A/T]AGTAATATTCTTTTT	26263
rs368069379	snp	A/T	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75906320	AGTGTACTCCTTGCC[A/T]TTGAGGGATTTGCTG	26263
rs368080698	in-del	-/C			intron-variant	FBXO22	GRCh38.p7	15:75906698	TCCAGGGAGCTGGCC[-/C]AGTATCCAAAGGCAG	26263
rs368269850	snp	A/G	4.94972e-05	0.00497455	missense, intron-variant	FBXO22	GRCh38.p7	15:75930075	TGTGCTTCTGATTTC[A/G]TCTGTGAATGAAGGG	26263
rs368407042	snp	C/G	5.02803e-05	0.00501374	intron-variant	FBXO22	GRCh38.p7	15:75914086	ATGGATGATATTTAT[C/G]ATTTTGCTACTGTAT	26263
rs368514675	snp	A/C			utr-variant-3-prime, nc-transcript-variant	FBXO22, NRG4	GRCh38.p7	15:75935193	ATTTAACCAAAGTTA[A/C]ATCTGTGTAACTCAT	26263
rs368732068	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75913707	CAAGATGCGCACACT[C/G]AGGTCCCAAGTTAGA	26263
rs368858406	snp	A/C	0.000153988	0.00877327	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914159	CCTTGAGAAGCTATT[A/C]CCCAAACAATGCCAA	26263
rs368885606	snp	C/T	0.00874735	0.0655527	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930499	GTTCCCAAATGTGTT[C/T]GGTCACAAAACTTTT	26263
rs369003682	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75925372	TGATCTGGTGATCTA[C/G]CTTGTAGATTGTTCA	26263
rs369034975	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75909550	GCCTGTTCAAATAAA[C/G]CAAGTGCATCTTTTG	26263
rs369056609	in-del	-/TAAAT			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901936	TCTATTAAGACAAAT[-/TAAAT]ATTTGCAAAAATGTA	26263
rs369069053	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902597	ATGTCATACTATCCA[C/G]CAGTGGGGGAAGGAG	26263
rs369105490	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902218	GAACATGCTGCTTCA[C/T]ACATCCATGTTCGTA	26263
rs369304460	snp	C/T	0.0558544	0.157504	intron-variant	FBXO22	GRCh38.p7	15:75921639	GCACTCCAGCCTGGG[C/T]GACAGCGAGACTCTA	26263
rs369526303	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75924695	GCAGCTCTACAGTGC[C/G]TGGCAGCTCTACCTG	26263
rs369704912	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901996	CTCTTTCCCTACTTT[A/G]TATCAGCCACAAAGA	26263
rs369970655	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75915622	AAATGTAAAAATTGG[C/T]CAGGCGCAGTGGCTC	26263
rs370092942	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933680	TTGACAAGACTAATC[A/C]GTATTTTATTATAAG	26263
rs370275260	snp	C/T	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75914422	TGTATAAATATCCAG[C/T]AGTCATTCATAAGAG	26263
rs370298080	in-del	-/A	0	0	intron-variant	FBXO22	GRCh38.p7	15:75925691	AAAAAAAAAAAAAAA[-/A]GCGATGCTGACATCT	26263
rs370309625	snp	G/T	0.000153988	0.00877327	intron-variant	FBXO22	GRCh38.p7	15:75929857	TTTTAAGGCTGTCTT[G/T]AACTGTTGCTCTTCA	26263
rs370351523	snp	A/G	0.00019338	0.00983121	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903997	TGCGGCGAGTGCCGC[A/G]GCTCCTCCGTAGACC	26263
rs370353595	snp	A/G			missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932810	CTGAGGCTGCGATGC[A/G]GCGCCTCAAAGCGGC	26263
rs370355890	snp	A/G	5.62562e-05	0.00530329	intron-variant	FBXO22	GRCh38.p7	15:75917402	TGAAGTAGGTAAGTT[A/G]CTTTTATTTATCATT	26263
rs370425347	in-del	A/TC			intron-variant	FBXO22	GRCh38.p7	15:75925414	CTCCCTGCTTTTTGA[A/TC]CCTTTAACTACTTGT	26263
rs370561742	in-del	-/AT			intron-variant	FBXO22	GRCh38.p7	15:75918773	TGCATGATCTCACTC[-/AT]GTGTGGAATCTAAAA	26263
rs370607982	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75919127	GTATGCACCACCATG[C/T]CTGGCTAATTTTTTT	26263
rs370749301	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75921032	CACAGACCTAGATGT[C/T]ACAGCCTACTATATG	26263
rs370760274	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927031	TTAAAGGTTTTGAGG[C/G]CAGCAAAGATTTTCC	26263
rs370789019	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932411	TGTACTTTCTAATAA[C/T]CGGATATGGGTTTCA	26263
rs370808107	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75917141	CTCAGATAGTGGCTT[G/T]TTAGCTTAATGATTA	26263
rs370860872	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903685	GGAGGTAGAAGCTGC[A/G]GTGAGCAGAGGCCGC	26263
rs370914225	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904497	CGTCCTCAGCGTGTG[C/T]CGCTTATGGAGGGAG	26263
rs370970944	snp	C/T	0.000155988	0.00883003	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903929	TCGGGTTCCTCCGAG[C/T]CGCCGTAGGACTGGT	26263
rs370973879	snp	C/G	1.65545e-05	0.00287697	intron-variant	FBXO22	GRCh38.p7	15:75904658	GGTGTCATGCACAGT[C/G]ATTTGCAGGTTGGTG	26263
rs371032210	in-del	-/GGCG			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903108	TGGTGCACAGCTTGG[-/GGCG]TGCTTCACAGCAATC	26263
rs371276673	in-del	-/A	0.482683	0.0914256	intron-variant	FBXO22	GRCh38.p7	15:75925675	CAGGAAGCTAGTGTT[-/A]AAAAAAAAAAAAAAA	26263
rs371508950	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75923455	CATTCTTTCACTTGC[G/T]ATCTTGTGTCCTAAT	26263
rs371567157	snp	A/C	0.000108293	0.00735765	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932664	TTTCATGAGATATTG[A/C]CACTTTTCTAAATTT	26263
rs371666062	snp	C/T	1.65745e-05	0.00287871	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75913259	TTCAGAAACTTTCAT[C/T]AGTCTGGAAGAGTGT	26263
rs371755802	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75905753	GGAAAATCACAGGCT[A/G]TTTTGTAGAACATCC	26263
rs371817159	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915605	ACCCCATCTCTACTA[A/G]AAAATGTAAAAATTG	26263
rs371906644	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75929292	TCCTTACTAACATAG[C/T]GAGACCCCATCTCTA	26263
rs372084450	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75913771	CCAGGTGACTGTTGA[C/T]GCAAATAGTAGTTAT	26263
rs372091749	in-del	-/ATA	0.00478085	0.0486577	intron-variant	FBXO22	GRCh38.p7	15:75929675	TAATTAAGATTTTGC[-/ATA]ATGTTTGTAAAAAAT	26263
rs372221349	snp	C/T	3.29935e-05	0.00406149	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914178	AAACAATGCCAAGTC[C/T]TTGGGATTGTGACCC	26263
rs372421282	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75924214	AGGGACTGGCTTCAG[G/T]GATTTGAGGAGGAGG	26263
rs372437072	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75928681	GCACAACAAACCCCC[A/G]TGACACACGTTTGCC	26263
rs372505349	snp	A/T	9.71638e-05	0.00696939	intron-variant	FBXO22	GRCh38.p7	15:75917413	AGTTACTTTTATTTA[A/T]CATTAACTGCTCATT	26263
rs372803008	snp	C/G	0.00052727	0.0162283	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929886	CATTTCTCTGCAGGT[C/G]TTTTAGATAACCCTG	26263
rs372921927	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908026	TGAACAGTGGAATGT[A/G]GTGTCAGCTGTCTTA	26263
rs373017734	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75932177	TATGATTGTGCCACT[C/G]CACTTCAGCCTAGCT	26263
rs373192132	snp	C/T	6.58935e-05	0.00573955	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904560	CGTAACCTGGATCTC[C/T]GCAGGCCTGGCGGAG	26263
rs373305733	in-del	-/AA			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902676	CATCGGTTTTTTAAA[-/AA]GAGTTAAGCATTAAG	26263
rs373567025	snp	C/T	0.000115305	0.00759205	intron-variant	FBXO22	GRCh38.p7	15:75904484	CTTTGTGCGTTTGCG[C/T]CCTCAGCGTGTGCCG	26263
rs373608006	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75916084	AAAAAAAAAAAGTTT[A/T]TTTCTTTTTTTATAC	26263
rs373620939	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75925463	CCAAGAGGGGTAAAA[A/T]AGAACTTTAATGACT	26263
rs373656786	snp	A/G	3.29549e-05	0.00405911	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929908	ATAACCCTGAACTTC[A/G]TGTGGTCCTTGTCTT	26263
rs373750491	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75921992	TGTTTTACAGTTAAC[-/T]TTTTTTTTTTTTTAA	26263
rs373916662	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922733	TGTGTGGGGAGACAC[C/T]GGAAGCGGGAGACCA	26263
rs374074953	snp	A/G	0.022594	0.103858	intron-variant	FBXO22	GRCh38.p7	15:75904155	GGACACGCCGTGGGC[A/G]TGTCCCAGGCTGGCG	26263
rs374314567	in-del	-/CA			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903259	TTTCACACACTAAGA[-/CA]ATTTTTTAAAAGCAA	26263
rs374351360	snp	A/C	1.65658e-05	0.00287795	intron-variant	FBXO22	GRCh38.p7	15:75904665	TGCACAGTCATTTGC[A/C]GGTTGGTGGTTCAGT	26263
rs374526182	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75920767	GGCGGAGGTTGCCGT[C/G]AGCTGAAGTCACGCC	26263
rs374563948	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920925	AGGTATGAAGAATAC[A/G]TATACAGTCATATGT	26263
rs374585584	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905224	TTTTTGTTGTCTGTT[C/T]TACCGGGAAGACAAC	26263
rs374592067	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75926986	AGAGTTACAATTGAC[A/T]TGTCCTTGTGTTATG	26263
rs374683342	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75908519	AGGCAATCCACCCAC[C/T]GTGGCCTCCCAAAGT	26263
rs374719379	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75905351	TGGCCCCCAACTTCA[A/G]AAGGGGAGCCAACAC	26263
rs374990547	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915664	CCCAGCACTTTGGGA[A/G]GCCGAGGTGGGTGGA	26263
rs375075495	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929143	TTCTTTTTCTCTTCC[G/T]ACCGCTCCAGTTTCT	26263
rs375164156	snp	C/G/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933230	TAGCTTTGATTGATG[C/G/T]TCTAAGATCACATGA	26263
rs375247904	snp	C/T			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935544	TGATCCAAGTAAAAT[C/T]TAAGGAAGAGGGAAA	26263
rs375266753	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75904909	GCTCACCGCAAGCTC[C/T]GCCTCCCGGGTTCAC	26263
rs375440844	snp	A/G	1.65045e-05	0.00287263	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914124	GCAAGGAAAAGAACT[A/G]GTATGGAAACAGCAC	26263
rs375525033	snp	A/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932304	GAGATGTTAATGTAA[A/G]CAATAGCAGAAGGCT	26263
rs375635712	snp	A/C	1.79281e-05	0.00299394	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933131	TTTCATAATATGTAA[A/C]TTTTGGGTTCTGCCT	26263
rs375771467	snp	A/C	1.65652e-05	0.0028779	stop-gained, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932726	GTGTGGTTGGACTGT[A/C]ATTTAGTGGACACCG	26263
rs376056704	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75928352	ATGGAATCAACCTGA[A/C]TGCCCATCAGTGATA	26263
rs376075604	snp	C/G	0.000155988	0.00883005	utr-variant-5-prime, nc-transcript-variant	FBXO22	GRCh38.p7	15:75903957	GGTTCCGGCGGGCTG[C/G]TGAGGAATGGAGCCG	26263
rs376518881	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919019	CTGGAGTGCGGTGGC[A/G]TGATCTCAGCTCACT	26263
rs376548905	snp	C/T			missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917230	TAACTTTTTCTCTAG[C/T]GACTCCAATGGGATC	26263
rs376640099	snp	C/T	0.000280299	0.0118352	missense, intron-variant	FBXO22	GRCh38.p7	15:75930064	AGTATGTCTTGTGTG[C/T]TTCTGATTTCGTCTG	26263
rs376678567	snp	C/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901968	GTAGTGATGCCGTCA[C/G]TGGTAAACTGTCCTC	26263
rs376886278	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75931418	CTGACCCAGTGCCCC[A/T]AAAGGAAGATGTATA	26263
rs376994772	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75925464	CAAGAGGGGTAAAAT[A/T]GAACTTTAATGACTT	26263
rs377008334	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75928704	CGTTTGCCTGTGGAA[C/G]AAACCTGAACATGTA	26263
rs377048066	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920509	ATATTCAATTGGCTC[A/G]TAATGTAGAACTCCT	26263
rs377201583	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75925458	AGCCACCAAGAGGGG[A/T]AAAATAGAACTTTAA	26263
rs377274979	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923971	ACAGCGATGTCATGC[A/G]GGTATGTGGCTAGCG	26263
rs377482704	snp	A/T	3.30874e-05	0.00406726	intron-variant	FBXO22	GRCh38.p7	15:75904653	CAAGGGGTGTCATGC[A/T]CAGTCATTTGCAGGT	26263
rs377597293	snp	A/C/T			intron-variant	FBXO22	GRCh38.p7	15:75916088	AAAAAAAGTTTATTT[A/C/T]TTTTTTTATACTAGT	26263
rs377674818	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904491	CGTTTGCGTCCTCAG[C/T]GTGTGCCGCTTATGG	26263
rs386383507	in-del	-/A			intron-variant	FBXO22	GRCh38.p7	15:75925676	AGGAAGCTAGTGTTA[-/A]AAAAAAAAAAAAAAA	26263
rs386785464	multinucleotide-polymorphism	CT/GG			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903905	CCGGGCAACCCTATG[CT/GG]GGCGTAATCGGGTTC	26263
rs397695138	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75929527	TGTTTTTTTTTTTTT[-/T]GTTCCCTACTGAGAG	26263
rs397776614	in-del	-/A			intron-variant	FBXO22	GRCh38.p7	15:75929322	CCAAAAAAAAAAAAA[-/A]TTTTTTTTAAAGATC	26263
rs397805120	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75909788	CTTTTTTTTTTTTTT[-/T]AAATTTCTGCGATAC	26263
rs527337996	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912300	AAATGAGTTAGGGAC[A/G]AGTCCCTCTTTTTCT	26263
rs527469165	snp	A/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918836	GGCAGGCACCAGGAT[A/C]TGGGGTGGTTGGGAG	26263
rs527512592	snp	A/G	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75911577	GTTTGTCTGTTATTG[A/G]TGTTTAGAAATGCTT	26263
rs527634001	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927517	GTAGTCACTTCTCTG[A/G]CATTGGCAGTCCTTG	26263
rs527660583	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921397	CCGGGCACAGTGGCT[C/T]ATGCCTGTAATCCCA	26263
rs527824328	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929650	CATTTAGTTTTTTTA[A/G]TAGAAAAAATAATTA	26263
rs527977166	snp	A/G			downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935621	TGATAAAAGTGGGCA[A/G]TCTAGTAGGCCAGTT	26263
rs527999497	snp	A/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75904330	TTCTCCATATCTGGC[A/T]CTTCTTCCGAACTAG	26263
rs528015239	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75909645	CTGGAATGAAGAAAT[C/T]ATAGGTGTTTAGTAA	26263
rs528062376	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925962	ATCTCTTGGTGGACA[A/G]CTACAGTAGTTAACT	26263
rs528338516	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902096	CTCTAAAGGCACCTT[C/T]TCCCAGAGGGATGGG	26263
rs528361133	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75905681	TGTTTCTTTAATCTC[C/G]TTTGATCTGGAACAG	26263
rs528437231	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75916904	GTGTATTTACTACCC[C/T]CCCAACTTTTTAATT	26263
rs528497045	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935760	AACATGCAAAGAATT[A/T]CAATAGAAATAAACT	26263
rs528867395	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75909799	TTTTTAAATTTCTGC[A/G]ATACATGTGCAGAAC	26263
rs529030319	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75926784	ATTCCTGTGAGACTT[C/T]AGTTAGTACTCAGTA	26263
rs529057378	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933468	CTGACTACCCCTTGC[A/G]TTGTTAGGTGATGTC	26263
rs529086940	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75913122	TGATTGCACTATGGA[C/G]TGGGTGATACTTCAA	26263
rs529164976	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75917495	GGTTCCTTTGGGAGA[A/C]TCTGAATTAAGTACA	26263
rs529303987	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928128	GTTTGTGGAGAAAAA[A/G]GAACACTTATACACT	26263
rs529490017	snp	G/T	0.00279162	0.0372561	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903889	GCTCAGTGCGCGCCG[G/T]CCGGGCAACCCTATG	26263
rs529605221	snp	A/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903892	CAGTGCGCGCCGGCC[A/G]GGCAACCCTATGCTG	26263
rs529663576	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930843	GCATCCTAGAGTGGT[G/T]ACATGGGGACAGACT	26263
rs529666737	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75931536	CAGAAGACGGATTTT[A/G]CCCCTCACAAACTTG	26263
rs529724599	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75931938	AAAATTATCCTCTGA[A/G]TGCAGTGGCTCATGC	26263
rs529775163	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902182	ACAGACTGGAGTTCC[A/G]GACAAGCAGGCATAG	26263
rs530101938	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908658	AGGTAGCTGAAGAGG[G/T]TCAGGTAGCTCAATA	26263
rs530405597	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932456	TGTGCATTGCCCCTT[A/T]GTATTTGTGACTGAA	26263
rs530412834	snp	C/T			synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929957	GGTGGGAGCCAGTAA[C/T]TATCTGCAGCAAGTA	26263
rs530437568	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75910555	ATGTTTGTTGGCCAC[A/G]TAAATGTCTTCTTTT	26263
rs530442383	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924978	TTTGAGTTTTATTTG[C/T]GGAGAGTCCCATTAG	26263
rs530464240	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923789	AAAAAGTATATGCAG[G/T]AGACACAGACTGTTG	26263
rs530669634	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931595	AGTCACTTAACCTTT[C/T]TGCGTCTTAGTTTCT	26263
rs530682564	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908170	ACCAGACTTTTAATA[C/G]TTGTTCAGGAGTAAG	26263
rs530749843	snp	A/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901888	TTTTGCAACAGATTG[A/T]ATTCAGAAGCAAATA	26263
rs530894993	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75917134	ACTTTTACTCAGATA[G/T]TGGCTTGTTAGCTTA	26263
rs530930152	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933654	AACTATTTTTGTTTT[C/G]GTCAGATAAATTGAC	26263
rs530991342	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902464	AACGCTTTGGGAGGC[A/G]GAGGCAGAGGGATGT	26263
rs531148036	in-del	-/CTC	0.00636936	0.0560724	intron-variant	FBXO22	GRCh38.p7	15:75909918	TATCCCTTCCCTAAT[-/CTC]CTCCCACTCCCTGAC	26263
rs531564500	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913077	TAGTTGTGTGGTTTT[G/T]AGTGAGTTTCTTAAT	26263
rs531587912	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914977	GCTGTCATTTATGTA[C/T]TGTTTTTGAGATGGA	26263
rs531623488	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75907355	AACATTACTTACAAT[A/G]CCAGGAGCATAAGTT	26263
rs531645098	snp	G/T	1.6525e-05	0.00287441	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914113	GTATTTTTACAGCAA[G/T]GAAAAGAACTAGTAT	26263
rs531915669	snp	A/G			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932284	ACAGCTGAAGTCGGG[A/G]GGAAGAGATGTTAAT	26263
rs531952192	snp	A/G	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75927114	TTTCCTGGTCGGGGG[A/G]AGGGGTGTGAGGCGG	26263
rs531976298	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	FBXO22, NRG4	GRCh38.p7	15:75935390	TACATACTGAGCTGA[C/T]GATCAGATCATAGAA	26263
rs532056660	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75904210	CCCACCAGGGCCGTC[C/T]CCGGCTCGCTCGCCC	26263
rs532200259	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913861	CTAAATTTGACATCA[C/T]TGGGGCAAAAGCAAT	26263
rs532338131	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75905229	GTTGTCTGTTTTACC[A/G]GGAAGACAACTGGGT	26263
rs532363417	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908203	ACCTGAGGCCTAAAA[G/T]CTTGCTGAGGGTTAT	26263
rs532390140	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75913117	TAATTTGATTGCACT[A/G]TGGACTGGGTGATAC	26263
rs532427418	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907471	CCATTGTAGTAAACT[A/G]CTGGTGAGACAAAAA	26263
rs532454609	snp	A/G	0.00478085	0.0486577	intron-variant	FBXO22	GRCh38.p7	15:75915557	GATCACTTGAAGTCA[A/G]GAGTTGGAGACCAGC	26263
rs532580095	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75910814	TGCCATTGCTTTTGG[A/T]GTTTTAGTCATGAAG	26263
rs532673117	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75914417	TTACCTGTATAAATA[C/T]CCAGTAGTCATTCAT	26263
rs532698150	snp	A/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934974	TCATACAATATTTGA[A/T]GTTGTTAAAGCATTC	26263
rs532820041	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75910653	AGTTCCTTGTAGATT[C/G]TGGATATTAGCCCTT	26263
rs532862946	snp	A/T			utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930683	CATTACTTCCTTTCC[A/T]TCTTGAATGAAAATA	26263
rs532903598	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930715	ATATCATTTTGAGTT[C/T]GAAACAATTAGGTGG	26263
rs532994519	snp	G/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918832	GAATGGCAGGCACCA[G/T]GATCTGGGGTGGTTG	26263
rs533166079	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75927448	AGCTAAAGCCCTGAG[C/T]GTCAGGAGATGTGGG	26263
rs533181544	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75921657	CAGCGAGACTCTATC[C/T]CAAAAAAATAAAATA	26263
rs533410827	snp	C/G	1.6473e-05	0.00286988	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904498	GTCCTCAGCGTGTGC[C/G]GCTTATGGAGGGAGT	26263
rs533509354	snp	A/C			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932315	GTAAACAATAGCAGA[A/C]GGCTTCGTTTAGTGG	26263
rs533512851	snp	A/T	0.00517822	0.0506191	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934885	AGCCTTAGAATTGAA[A/T]GGATTATTTTAAACA	26263
rs533723753	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902835	GTTTCTGCCCAAGAT[C/T]TGGCGATCAAATCAG	26263
rs533788016	snp	C/G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918357	AGTCATTGGTGGATG[C/G/T]GAGGGGAAGCACAGA	26263
rs533962949	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905308	AGCCAAATATTTCAA[C/T]TTCTGATCCTGTACT	26263
rs533971843	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911005	AGTTTTCTGAACACC[A/G]TTTATTAAATAGTGA	26263
rs534096936	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928276	AGGAATATAAATTAT[A/T]CTGTTATAAAGACAC	26263
rs534097314	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919208	AACTCCTGGCCTCAA[A/G]TGATCCACCTGCCTC	26263
rs534147556	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918310	TTTTTACAACTATCC[A/C]TGACAATGTGGAAAA	26263
rs534483899	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75931719	ATGCTTTATTACTTT[G/T]ATCAATGTTGTATTT	26263
rs534484070	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75923055	TGCTGCCTTTTTTGT[C/T]CAGAGAGGTGACATA	26263
rs534491319	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902919	CTGTGTCTGCTGTGC[C/T]TCCATTTCTTGGTGG	26263
rs534521595	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924033	AAGATTTGAAGGTGC[A/G]GGTTGGAAGATCAGA	26263
rs534624125	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75905511	GGCTTACAGACAGAC[A/G]TAACTACGGTGCAGC	26263
rs534637256	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930980	CTGGACTGCCAGGGA[A/G]GAGGAAGAGAGGAAG	26263
rs534677493	in-del	-/CACCACA	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75910337	AGATCCTTGAGGAAT[-/CACCACA]CTGTCTTCCACAATG	26263
rs534720109	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917493	TAGGTTCCTTTGGGA[G/T]AATCTGAATTAAGTA	26263
rs534739131	in-del	-/T	0.330482	0.236691	intron-variant	FBXO22	GRCh38.p7	15:75929514	CTGTGTAAACCAGTG[-/T]TTTTTTTTTTTTTGT	26263
rs534871080	in-del	-/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75921762	TTTCTCCACCTTTAA[-/T]TTTTTTTTTAACTTT	26263
rs534985676	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926468	TTAAGTTGGGGTAGG[A/G]GAAAGTGATTCTACT	26263
rs535093734	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902263	TTTCTTTAGGGAGAG[A/G]ATTTTAGCATTATGT	26263
rs535116490	snp	C/T	0.000148262	0.00860865	synonymous-codon, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932868	CTTCATGTTTGCATG[C/T]GTTGGCAGGGGCTTT	26263
rs535250758	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925430	CCTTTAACTACTTGT[C/T]TTGAATTCTGCCAGC	26263
rs535259752	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75906179	TTGAGCACTTTTCTT[G/T]TTTTCTGGCACAAGA	26263
rs535282323	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75916556	GCCTTATCTCCAAAT[A/G]TAGTCACATGGGGGG	26263
rs535457769	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902586	TGCCACTGACAATGT[C/G]ATACTATCCACCAGT	26263
rs535545217	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75915857	GTGAGCCGAGATCAC[A/G]CCATTGCACTCCATC	26263
rs535654255	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75908433	GCATGCAGCCATACC[C/T]GGTTACTTTTTGTAT	26263
rs535850007	in-del	-/GTTAGC	0.00636936	0.0560724	intron-variant	FBXO22	GRCh38.p7	15:75920011	TATGTAAATAGCAGA[-/GTTAGC]GTTAGCAGAAATGTT	26263
rs535988118	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927096	TGCCTAAAGCCTTTT[C/G]CCTTTCCTGGTCGGG	26263
rs535992713	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917793	TTTAGAAGTTTTTAG[A/C]ATACGCGGGTTAGTT	26263
rs536050247	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934599	TATGATAAAAATGCT[G/T]GGAAGAGTCCTTTAA	26263
rs536253693	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75931824	TCAAATTAAGCTGAA[C/T]TCTAGACTCAAAGCA	26263
rs536392713	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921127	GAATACTGTAGGCAG[C/T]TGTAACACAATGGTA	26263
rs536618706	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931207	TCAGACTTATAACAT[C/G]TGAGGTGCTAGCTTG	26263
rs536690717	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75904370	TGACACCTACCTACC[C/T]CGGGGACTTTGGATC	26263
rs536714391	snp	A/G	3.30256e-05	0.00406346	missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933055	GATGATCTGTTTCAT[A/G]GCTATACAACAATAA	26263
rs536784247	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922919	CCAGAAATAGGAACA[A/C]TGGGACAGGAGGAGC	26263
rs536854870	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930891	ATAAGAATAATGTAA[A/G]TCATCCTAGTTATAG	26263
rs536915792	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908550	GCTGATATTACAGGC[A/G]TGAGCCACTGTGCCT	26263
rs536993502	snp	A/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75915157	TGTATTTTTAGTAGA[A/C]ACCGGGTTTCACCAT	26263
rs537024658	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915329	ATTGTCATTTTTAAT[C/G]TTCACTGAAAGATTT	26263
rs537063276	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75907692	CTTGAGGTCAGGAGT[C/T]AGAGAACAGCCTGGC	26263
rs537578449	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932224	TCTAAAAAAATAAAA[C/T]CACCCTCCATTATTA	26263
rs537702326	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903669	GGATCGCTTGAGCCT[A/G]GGAGGTAGAAGCTGC	26263
rs537881669	snp	A/C			intron-variant	FBXO22	GRCh38.p7	15:75927418	TTGAGATTTAGAAGT[A/C]ATGAGGTTTCTAAAA	26263
rs537906637	snp	A/C/T			intron-variant	FBXO22	GRCh38.p7	15:75918959	GTGACCATATATTCT[A/C/T]TTTTTTGTTTGTTTT	26263
rs537945620	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75922853	AGGGAAGCCTCAGTA[A/G]TTACTTTTGAGTTTT	26263
rs538035708	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904162	CCGTGGGCATGTCCC[A/G]GGCTGGCGGGGTGGG	26263
rs538036417	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920645	TGGACAATATAGTGA[A/G]ACCTCACCTCTACAA	26263
rs538062036	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75913411	CTGGGACTGCCACCT[A/G]TAGTATGCATCAATA	26263
rs538090135	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911744	CTCTCTTCCTATTTG[A/C]ATATGCTTTATTCTT	26263
rs538154128	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75919013	CCCAGGCTGGAGTGC[A/G]GTGGCATGATCTCAG	26263
rs538199048	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929165	CCAGTTTCTGCTTCT[A/G]TGGTCACACTGCCTT	26263
rs538498321	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75929549	TACTGAGAGCCAGCT[A/T]GCACCTTGGTCTACC	26263
rs538568286	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919974	TGAACTTTAATGGCA[A/G]TAGAGAGTTAAGGCT	26263
rs538612496	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75929244	ATTGGATTTAGAGCC[C/T]ACGTGGATAGACCAG	26263
rs538639540	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920835	CTCAAAAATAAATAA[A/G]TAAATAAAAATTTAT	26263
rs538775902	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928672	AAATAATCTGCACAA[C/T]AAACCCCCATGACAC	26263
rs538832007	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75905641	AAAGATCTGTTCCCA[A/G]TTGCAATTTGCTCTG	26263
rs538840705	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914259	TTAATGTGGGGTCCT[G/T]TGGATTGGTGAGTTA	26263
rs539099164	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905236	GTTTTACCGGGAAGA[C/T]AACTGGGTGTGTCTT	26263
rs539226094	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909060	ACTTCATTTTATTCT[G/T]GTAGTAAAAAATATT	26263
rs539265361	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909931	AATCTCCCACTCCCT[A/G]ACAGGCCCTGGTGTG	26263
rs539365402	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913505	AATTGAAACAAATTC[A/G]TTAGAAAGGTGTTGT	26263
rs539444799	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75912579	TTTATGGTATTCTCT[C/G]ATGGTAGTCTGTATT	26263
rs539598732	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917368	CAAAGAATTTAACAT[C/T]AGAAAGACATCAACT	26263
rs539654921	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927702	AAAGTAATATTCTTT[C/T]TACTGTCCAAGTCAG	26263
rs539826500	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911872	TGCTTCCAGCTTTTG[C/T]CCATCTAGTATGATA	26263
rs539845757	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917973	GAGGTAAAGGGTTGG[C/T]TTAATGTCTAAGCTT	26263
rs539858756	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75904302	CCTGAGGGGCGAAGT[C/T]CCCCTTAAGGTTTTC	26263
rs539970893	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919162	TTTTTATTAGAGATA[G/T]GGTTTTACCATGTTA	26263
rs540089722	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75924851	ATAGCAAACAGTTGA[C/T]TCACACCTGGGATCC	26263
rs540558759	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918719	GGATGAACCTGGAGG[A/T]TGTTAAGTGAAATAA	26263
rs540610272	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75910477	AACTGGCATGAGATG[A/G]TATCTCATTTTGGTT	26263
rs540621867	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75931605	CCTTTTTGCGTCTTA[A/G]TTTCTCACTAATCCA	26263
rs540658111	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934649	CTAGTTCCTGAGGCA[A/C]GTCCAAAGAAAAATT	26263
rs540695077	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927939	TCATTTTCCTGTCCC[C/G]AAAGCACCCGTTTGG	26263
rs540794351	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911372	TATGGGCATTTTCAC[A/G]ATATCGATTCTTCCT	26263
rs540833172	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903838	GGCGTTGCCACGCCC[A/C]CCTTCCCCGTCCAGC	26263
rs540958941	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922273	TGCATATGCTTACTG[G/T]GCGTGTCACCACGCC	26263
rs541038725	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902125	GGAGGCTGGGGAGTT[C/T]AAAGAGTTAGCTGAG	26263
rs541039902	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75908631	CAGATTCAGATGACT[C/T]GAAGGTCAGGCAGGT	26263
rs541202300	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916306	AAATACCACAGACTG[A/G]GTGACTTAAACAACG	26263
rs541289656	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903678	GAGCCTGGGAGGTAG[A/G]AGCTGCAGTGAGCAG	26263
rs541312602	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921375	TAATTGAAACATTTT[C/T]GTTTGGCCGGGCACA	26263
rs541532032	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75913426	GTAGTATGCATCAAT[A/G]TATCTATCTTTGAAC	26263
rs541597873	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932287	GCTGAAGTCGGGGGG[A/C]AGAGATGTTAATGTA	26263
rs541597972	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923623	TTCAAAATAACACTC[C/T]TGCTATGATGTGGTG	26263
rs541746699	snp	A/C/T	0.000283163	0.0118956	intron-variant	FBXO22	GRCh38.p7	15:75913299	AAGAGAGGTAAATAT[A/C/T]AAAAGAAAAGCTTTT	26263
rs541766464	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931495	AAGAGGAAATGTGAT[A/G]AAGTTTTAAGAGCAG	26263
rs541834387	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902424	AAAAAACTGGCTGGG[C/T]TTGGTGGCTCATACC	26263
rs541853231	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75920383	TGAAGGCCTTGGAGT[A/G]AGCCAGTCCAGGGCA	26263
rs541859823	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75901954	ATATTTGCAAAAATG[C/T]AGTGATGCCGTCACT	26263
rs542145728	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75907289	TAATAATTTTCCTAT[A/G]CCCTTATAGAGTTGT	26263
rs542184164	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75924844	TAGTTATATAGCAAA[C/G]AGTTGACTCACACCT	26263
rs542221439	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910177	TATCACTGATGGGCA[C/T]TTGAGTTGGTTTCAA	26263
rs542272179	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75905725	GCTTGATTTTTCCCA[A/G]TCTTGACACTTAGGA	26263
rs542371991	snp	A/G	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75925851	GGGGCTTGGTGGATG[A/G]AAAATTCCTAAGAGG	26263
rs542448394	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75917003	TTTAGCAGTTGAAAA[A/C]ATTTTGCAACATTTA	26263
rs542580758	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922436	GGCTTCCAGAAGCAG[A/G]TGGTATTTAAGCCCT	26263
rs542585015	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75905115	GGCGTGAGCCACCGC[G/T]CCCGGCATGTTGGGC	26263
rs542613012	snp	C/T	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75914939	TTTACAATAGAGATA[C/T]ACAAAGCAGTAAGTA	26263
rs542746382	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913057	CAGGTTGTTCAGTTT[C/G]CATGTAGTTGTGTGG	26263
rs542781060	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933577	TGCCTTTCAGTTTTA[C/T]GAATTTTTTCAGAAG	26263
rs542783871	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930381	GTTTCCTCCTTTAAA[A/G]GAAACACATGGTTAG	26263
rs542808924	snp	C/G	0.00478085	0.0486577	intron-variant	FBXO22	GRCh38.p7	15:75928761	TTGATAGTCTATAAA[C/G]AAGCTGCCAGAGGCT	26263
rs542835504	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75928080	CTAGGCAGAATGGCT[A/G]TTAAAAAGTCAAAAA	26263
rs542974228	snp	C/T	0.00517822	0.0506191	intron-variant	FBXO22	GRCh38.p7	15:75928037	TAGAGAAATGCAAAT[C/T]AAAACCACAATGAGA	26263
rs543100065	snp	A/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75929679	TAAGATTTTGCATAA[A/T]GTTTGTAAAAAATGG	26263
rs543312143	snp	C/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75909927	CCCTAATCTCCCACT[C/G]CCTGACAGGCCCTGG	26263
rs543378584	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929434	ACCACACTATAAGTG[C/G]TTAGCGCCTTTTCTC	26263
rs543419846	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908188	GTTCAGGAGTAAGAA[A/C]CCTGAGGCCTAAAAG	26263
rs543424214	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906695	TCATTCCAGGGAGCT[A/G]GCCAGTATCCAAAGG	26263
rs543588223	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923374	GATGTCAGCAGTTTT[G/T]GCTTATTCCAAGGCA	26263
rs543645948	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913794	GTAGTTATACTGCAA[C/T]ATCAGCTGAACAGAA	26263
rs543691615	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928844	TCTGCCACCTCCTAG[C/T]GGTAGCAGCTTTTAG	26263
rs543727647	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920393	GGAGTAAGCCAGTCC[A/G]GGGCAACATAGCCCA	26263
rs543764410	snp	C/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75924617	CTGGCAGTGCTCATG[C/G]ACTTCTTCCTCTAAA	26263
rs543769386	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918789	TGTGTGGAATCTAAA[A/G]ATGTTGCTCTCATAG	26263
rs543802714	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916139	AAAAATTAGAAGATT[C/G]AGATAAGCAAAAGCA	26263
rs543805724	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919467	AATAGAAGGTAGTCA[A/G]CCTTAAAAGATTGCA	26263
rs543809897	snp	A/G	0.0023933	0.0345097	intron-variant	FBXO22	GRCh38.p7	15:75911398	TTCCTATCCTTGAGC[A/G]TGGAATGTTTTTCCA	26263
rs544058598	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75916199	TATGATGTTAACCTC[C/T]ATTTATATATGTATG	26263
rs544282150	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75935060	ATGGTTGTAACCTTA[C/G]TGCAAAGTAAAAAGG	26263
rs544320220	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927360	AGGATGTTTAGTGGA[C/T]GTTGTAAAAGAGCAT	26263
rs544453404	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908821	GTGGAATTTTGAACA[C/T]TGGCATTCAGTTTAC	26263
rs544583079	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924549	GCTTTGCCCACCAAA[A/G]CACAGTCTGAAAGCC	26263
rs544612400	snp	C/G	1.6473e-05	0.00286988	synonymous-codon, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904533	GCGCAGAGTATTGCG[C/G]ACCCATCGGAGCGTA	26263
rs544686470	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912952	TGTGTCCCAGAGATT[C/G]TGGTACATTGTGTCC	26263
rs544773236	snp	A/C	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75904399	TCCCGCAGGGATCTC[A/C]TGCTGCTGCGCCAGC	26263
rs545125653	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919542	AGGGCAAGTTTTTCA[A/G]TTTTTCTAAACCTCC	26263
rs545181699	snp	C/G	0.00358779	0.0422022	intron-variant	FBXO22	GRCh38.p7	15:75927493	CTGTCATTATATTGT[C/G]CTGGGGTAGTAGTCA	26263
rs545249183	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903415	GCGGTGCCAGGGCAG[C/T]GAGAGGCACAGGCAC	26263
rs545302328	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75931974	ATCCCAGAACTTTGG[A/G]AGGCTGAGGCAGGAG	26263
rs545470204	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75908849	TACATTTTCTGAAAA[C/T]GCTGTGTGGACCAAG	26263
rs545574060	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902003	CCTACTTTATATCAG[C/T]CACAAAGAAAGAACG	26263
rs545828520	snp	A/T			missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75929959	TGGGAGCCAGTAATT[A/T]TCTGCAGCAAGTAGT	26263
rs545857307	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75906487	CAGGTGCATCCTTTT[C/T]GAATCAAACGCAGGA	26263
rs546179125	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925933	CAGTTTCATCCTATT[C/T]CAAAACCAAAGACAT	26263
rs546200952	snp	A/G	0	0	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903738	ACAGCATTAGACCCA[A/G]TCTCAAAAATGAAGA	26263
rs546212074	snp	C/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75917145	GATAGTGGCTTGTTA[C/G]CTTAATGATTATCTT	26263
rs546214249	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75914575	CAAAGCTGGGCCTTA[C/G]TAGGAGACTTCTGTT	26263
rs546318753	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926001	GTTGCCAATCCTACA[C/T]GGCAGGTCAGTTTAT	26263
rs546343103	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932566	ATGAGGGTGAGCCTC[A/C]GATTAACCATAGGCT	26263
rs546348911	snp	C/T	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75917799	AGTTTTTAGAATACG[C/T]GGGTTAGTTCTTTGT	26263
rs546364045	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903071	TAGTTTCCAGGTGAA[C/T]CTGATGTCCCTGGCG	26263
rs546405370	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916501	TTGGATTAGGGTCCT[A/G]CCCTTGTGACCTCAT	26263
rs546429412	snp	C/G	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75910320	ATGGTATTTCTCTTT[C/G]TAGATCCTTGAGGAA	26263
rs546508599	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931741	GTTGTATTTTCTTTT[G/T]TAAGGATATTTCATT	26263
rs546512193	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75926666	ATCCGGGAAAAACAC[C/T]AGTCACAAACGAGTG	26263
rs546577690	snp	C/G	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75909767	CAGCAGTTTGGATGG[C/G]GTGATACTTTTTTTT	26263
rs547088753	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934570	AAATATTTTTCTCTT[A/G]CTATTTATATATATA	26263
rs547356081	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902545	ACCAAAAAAAAGAAA[A/G]AAACCACAGCTACTC	26263
rs547373766	snp	C/G	3.45435e-05	0.00415579	intron-variant	FBXO22	GRCh38.p7	15:75913153	GGGACTATGCAGAAG[C/G]ACTGATGGATTCATG	26263
rs547428610	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75928794	AGTGAAACCTGGGAG[C/T]TGTGGGCAGAGCAAG	26263
rs547473771	in-del	-/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75905560	ATCACTGATACATTT[-/C]TACCATTTTATCCTC	26263
rs547572923	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907556	CTAGTGGACATGGGT[A/C]CTTTTATAGCCATAA	26263
rs547668889	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75907164	CTGTTAATAGCCAGA[C/T]AGACTTAGTTGTGAA	26263
rs547792168	snp	A/G			missense, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932776	CTCCTCAACGAGGAC[A/G]TCAGTGATGAGAAGA	26263
rs547866288	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915579	GAGACCAGCCTGGCC[A/C]ACATGGCAAAACCCC	26263
rs547905115	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908253	GTTGCCACTAAGACC[C/T]AAATCTGTTTTTTGT	26263
rs547994526	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930853	GTGGTGACATGGGGA[C/T]AGACTGTTGCAGATC	26263
rs548101168	snp	G/T	0.00318978	0.0398085	intron-variant	FBXO22	GRCh38.p7	15:75921678	AAATAAAATAAAATT[G/T]TTCTTTAATAATAAA	26263
rs548119373	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931563	CTTGTTTTACTACTA[C/G]CTAGCCTTATTACTT	26263
rs548160883	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922771	GTCCAGGCAAGAAAT[A/C]ACACTAGGGCATGAG	26263
rs548233279	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75915099	CAGCCTCCCAAGTAG[C/G]TGGGATCACAGGCGC	26263
rs548462482	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908312	AGAGTCTCGCCTGTC[A/G]CCCAGGCTGGATTGC	26263
rs548524923	in-del	-/A	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75906897	AAGCTATTAAATTAT[-/A]GACTGCAAATGCATT	26263
rs548845213	snp	A/G	3.29881e-05	0.00406115	missense, intron-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904619	TTCGCGTGGTAGCAG[A/G]GGAGCTTGAGGCAAG	26263
rs548890828	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915162	TTTTAGTAGAAACCG[G/T]GTTTCACCATGTTGG	26263
rs548929372	snp	A/C	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75915735	TGAAACCCCATCTCT[A/C]CTAAAAATACAAAAA	26263
rs548929834	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75914003	TATTTAGAGCATTCT[C/T]GTGTTAAATGACTTA	26263
rs548978499	snp	A/C	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75918333	GTGGAAAAAAAAAAA[A/C]AACTTGCAAGTCATT	26263
rs549054489	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920529	GTAGAACTCCTACAT[C/T]AATTTTATTCAGGCT	26263
rs549097371	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921460	TTGCGATCAGGAATT[A/T]GAGACAAGCCTGGTC	26263
rs549161797	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75904074	TGTGCTCACCTTCCT[A/G]CCCGCCAAGGCGTTG	26263
rs549183230	in-del	-/AG			intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932196	TTCAGCCTAGCTAAC[-/AG]AGAACCCTATCTCTA	26263
rs549287035	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75918318	ACTATCCCTGACAAT[C/G]TGGAAAAAAAAAAAA	26263
rs549293027	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927532	GCATTGGCAGTCCTT[A/G]TTTGTAAAATAAAAC	26263
rs549328097	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918905	GTTTTGGAGGAATAA[C/G]TTCTTGAGGTCTGTT	26263
rs549736579	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907404	AATATTCTTTTATTA[A/G]TATCATTATTAAAGT	26263
rs549857903	snp	A/G	1.64909e-05	0.00287144	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75914138	TAGTATGGAAACAGC[A/G]CTTGCCCTTGAGAAG	26263
rs549925455	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75929789	AAATTGCCCTTAAGG[G/T]GGAGTGCAAGTCAGT	26263
rs550005902	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905203	ACCTGCTTCCCTTGA[A/C]GCAACTTTTTGTTGT	26263
rs550132558	snp	C/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75912501	GTTTAGTGTTGGAAG[C/G]GGGTATGTGTCCAGG	26263
rs550213995	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907725	ACATGGTGAAACCCC[A/G]TCTCCACTAAAAAAA	26263
rs550231126	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929828	ATTTTGCAGCATGTA[C/T]AAAATAATTTCTGTT	26263
rs550252123	snp	A/G	1.65244e-05	0.00287436	synonymous-codon, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917297	ATCTGGTTTTGCTTT[A/G]TTATTCCCTCAAATT	26263
rs550275755	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902635	GAAATAATTGTTTTC[C/T]ATAAAAATATTTCGT	26263
rs550290646	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75918048	CTCAAGGAAAGCAGC[A/G]TTTAGCCTTTTATCT	26263
rs550474705	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75920668	CTCTACAAAAAAACT[A/G]AAAAACTAGCCAAGC	26263
rs550556461	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903470	AGGAGGCCTCCTAGA[A/G]AGTTGCCAGGAGCGG	26263
rs550623070	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925450	ATTCTGCCAGCCACC[A/G]AGAGGGGTAAAATAG	26263
rs550661672	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75928148	ACTTATACACTGTCG[A/G]TGGGAGTGTAAATTA	26263
rs550704447	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926211	TATGGCGGGTGGCCC[A/G]GAACATTGGGTCCTT	26263
rs550839325	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75917532	ACTGGAGATGTGGCT[A/G]ATTCAAACAGGTGAT	26263
rs550866527	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933559	GCTGGAGAAATTTTT[A/C]TCTGCCTTTCAGTTT	26263
rs550911856	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75919020	TGGAGTGCGGTGGCA[C/T]GATCTCAGCTCACTG	26263
rs550935253	snp	G/T	0	0	missense, nc-transcript-variant, utr-variant-5-prime	FBXO22	GRCh38.p7	15:75903992	GCTGCTGCGGCGAGT[G/T]CCGCGGCTCCTCCGT	26263
rs551006466	snp	C/T	0.00159617	0.0282053	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75930871	ACTGTTGCAGATCAG[C/T]ATCTATAAGAATAAT	26263
rs551151324	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75923646	ATGTGGTGATCATTT[G/T]GGAGTACAAGAGTGG	26263
rs551172658	in-del	-/CAGTGCCTGGCAGCTCTA	0.00279162	0.0372561	intron-variant	FBXO22	GRCh38.p7	15:75924671	GCTCTAGACTCAGAG[-/CAGTGCCTGGCAGCTCTA]CAGTGCCTGGCAGCT	26263
rs551182427	snp	G/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918833	AATGGCAGGCACCAG[G/T]ATCTGGGGTGGTTGG	26263
rs551224744	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75911558	ACTCATGATTTGGCT[C/T]TCTGTTTGTCTGTTA	26263
rs551368126	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926369	CCCTCTGTTATTTAC[C/T]GGTAGCACCAGGTAG	26263
rs551444829	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75928234	TACCATTTGACCCAG[C/T]AGTCCTATTACTGGG	26263
rs551445437	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75920480	ATGTGTTGATGTTGA[C/T]GAGATGACTATCTAT	26263
rs551481723	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929049	GAAATTTATTCTGCA[C/T]AGTTCAGGAGGCCAG	26263
rs551515555	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918214	GGACTTAAACCAGCT[A/G]GAGTAAAAAATTGTG	26263
rs551556187	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902478	CGGAGGCAGAGGGAT[A/G]TCTTGAGGCCAGGAG	26263
rs551683213	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934365	GACTATCTACCTCCA[A/G]ACTGTTTTACAAGAG	26263
rs551720383	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75926941	TTGCAATGGACATTA[C/T]CAGTGTGGAATTGAA	26263
rs551722189	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75904225	CCCGGCTCGCTCGCC[C/G]TACCTGAGGTGACCC	26263
rs551798595	in-del	-/T	0.0252718	0.109532	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933725	CTTTCCTTAAAAATA[-/T]TTTTTTTTTCACCTA	26263
rs551877750	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932499	TTCTCTTGATCTGCC[G/T]TGTGCATTTTTTATG	26263
rs552005687	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923994	GGCTAGCGCAGCTGT[A/G]TAGTACCATTGACTA	26263
rs552012513	in-del	-/TG	0.00557542	0.0525036	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932338	TTTAGTGGATATCTT[-/TG]TGTATATTAATAAAA	26263
rs552113168	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924979	TTGAGTTTTATTTGC[A/G]GAGAGTCCCATTAGA	26263
rs552285871	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75911186	GTAGTATAGTTTGAA[G/T]TCAGGTAGCATGATG	26263
rs552600664	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75908110	GTGAATTAGGAAGGA[A/G]AATTCAGCAGTTGCT	26263
rs552782243	snp	C/T	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75907936	GATAAAGAGTGAGAC[C/T]GTGTCTCAAAAAAAA	26263
rs552829008	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916401	TTACTTACAGCTGCT[C/G]TCTCACTGTGTTCTC	26263
rs552899409	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908357	GGCTCAGTGCAACCT[C/T]CACCTTCCTAGTTCA	26263
rs553003880	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902230	TCATACATCCATGTT[C/T]GTAAGATGCCAGTGA	26263
rs553022364	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75915856	AGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAT	26263
rs553515017	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75923915	GAATGGACAGGATGT[A/G]GTGACTGATGAGATG	26263
rs553522159	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916937	AAAAATATGGAGAAG[C/T]TGAAAGAATAATAGA	26263
rs553788095	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930183	TTCCATTTTGTAGTA[A/G]ACATTGGCTAAGGGG	26263
rs553849768	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75920097	CCCTTAAAACTGACC[C/T]ATTGTTAAGTGTAAA	26263
rs553883280	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75928689	AACCCCCATGACACA[C/T]GTTTGCCTGTGGAAC	26263
rs554105401	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904738	AAGGAACATCTCGTT[C/T]CGTGAAAAGATTTTG	26263
rs554159016	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913514	AAATTCGTTAGAAAG[A/G]TGTTGTTCTCAATTT	26263
rs554195819	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905671	GAGTAAGTCCTGTTT[C/G]TTTAATCTCCTTTGA	26263
rs554307257	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906443	TACAATTATATTTCT[A/G]TATATATGTGGAGGC	26263
rs554626056	snp	C/T	0.000164957	0.00908026	synonymous-codon, intron-variant	FBXO22	GRCh38.p7	15:75930074	GTGTGCTTCTGATTT[C/T]GTCTGTGAATGAAGG	26263
rs554682449	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921172	TGAACATATCTAAAC[A/T]TTAAAAAGGTACAGT	26263
rs554714335	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75923302	GGAAGGAAAAACAAC[C/T]CCAGAATTATTGTGC	26263
rs554775617	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	FBXO22	GRCh38.p7	15:75931214	TATAACATCTGAGGT[A/G]CTAGCTTGTAAGTGT	26263
rs555235809	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903637	TAGTTAAAGCTACGA[C/G]GGAGGCTGAGGCGGG	26263
rs555271206	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907670	GAAAGCCGAGGCAGG[C/G]AAATCACTTGAGGTC	26263
rs555400758	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75911068	TGTCAAAGATCAGAT[C/T]GTTGTAGATGTGTGG	26263
rs555433907	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912909	GTGCATTTAGTGCTA[C/T]AAATTTCCCTGTAAA	26263
rs555440806	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75934963	ACAGGGTAATTTCAT[A/G]CAATATTTGATGTTG	26263
rs555618737	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927821	ATCTGCATACCCTTT[A/G]TTTCCTTAAGTAACT	26263
rs555655485	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919349	GGTAACTGTGAGATA[A/G]TGCATATGTGAATTA	26263
rs555656660	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934012	TGCAGAGAGCACCAA[C/T]TTTCCTTCAATATCC	26263
rs555824722	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904334	CCATATCTGGCTCTT[C/T]TTCCGAACTAGCGCC	26263
rs555935208	snp	A/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75928583	ACTGGGGCCTACCAG[A/T]GGGTGGAGGGTGTGA	26263
rs556167489	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919478	GTCAACCTTAAAAGA[C/T]TGCAGGCTTGTAGCT	26263
rs556217547	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904221	CGTCCCCGGCTCGCT[C/T]GCCCTACCTGAGGTG	26263
rs556230813	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927941	ATTTTCCTGTCCCCA[A/G]AGCACCCGTTTGGTA	26263
rs556417122	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903674	GCTTGAGCCTGGGAG[G/T]TAGAAGCTGCAGTGA	26263
rs556458472	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912935	GTAAACACTGCTTTA[G/T]CTGTGTCCCAGAGAT	26263
rs556562789	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75908570	CCACTGTGCCTTGCC[C/T]GTAAATCTCTTTTTC	26263
rs556567660	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920042	AAAGCTATTCTAAAT[G/T]AAGGATGCCAAACTT	26263
rs556573247	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75904714	TTTAAATCCCAGTTT[G/T]GTTAATTAAAGGAAC	26263
rs556696797	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916558	CTTATCTCCAAATAT[A/C]GTCACATGGGGGGTT	26263
rs556858228	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916007	AACCGGGAGGCAGAG[A/G]TTGCACCACTTCGCT	26263
rs556876378	snp	C/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75912319	CCCTCTTTTTCTGTT[C/G]TTTGGAATAGTTTCA	26263
rs557049322	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902274	AGAGGATTTTAGCAT[C/T]ATGTTAATTATCTAA	26263
rs557344264	snp	G/T	7.30087e-05	0.00604144	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933147	TTTTGGGTTCTGCCT[G/T]TTTCAGAAAATGGAA	26263
rs557351222	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75911244	ATTGTCCTGGCTATA[C/T]AGGCTCTTTATTGGT	26263
rs557492232	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910038	TTTCTGTTCCTGTGT[G/T]AGTTTGCTGAAAATG	26263
rs557510338	snp	A/G	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75918382	CACAGAACAAGAGGC[A/G]TTAGCAGCAAAGACT	26263
rs557573184	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75916464	GGTGTCTCTTCCTCC[C/T]CTTCTCAGGACACTA	26263
rs557653085	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75909089	TTTGAAAATAGCTAG[C/G]TTGGAAAAATATATC	26263
rs557791076	snp	A/G	1.76129e-05	0.00296752	missense, nc-transcript-variant	FBXO22	GRCh38.p7	15:75917385	GAAAGACATCAACTC[A/G]CTGAAGTAGGTAAGT	26263
rs557889224	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75929580	AAGAGTTGCTGCTCA[C/G]TACATAGCTGCTTCA	26263
rs557955585	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919172	AGATAGGGTTTTACC[A/G]TGTTAGCCAGGGTGG	26263
rs557974868	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75927756	AAATGGACCAGAGGC[A/G]GTTTCCCAGAATAGG	26263
rs557992551	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911898	TGATACTGGCTGTGG[A/G]TTTGTCATAAATAGC	26263
rs558018496	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75916640	CAATCTGTAATATCT[A/G]CCTGTAAAATTCAGA	26263
rs558143960	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75904325	AGGTTTTCTCCATAT[C/T]TGGCTCTTCTTCCGA	26263
rs558284266	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918608	TGGAATTAACCTAAG[C/T]GTCCATTAGCTGATG	26263
rs558435651	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930145	AAAAAACGTGTTTAA[A/T]GAATTATTAAGATAA	26263
rs558492387	snp	C/T			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903546	GTATCGCTTGAGCCC[C/T]GGAGTTTCAGACCAG	26263
rs558493151	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75905397	CTCGAACTGTGGAGT[C/T]AGAGGGGCTGCAGGG	26263
rs558516288	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75922157	TGGCACTGCAATAGG[C/T]TTGTTTACAACAGCA	26263
rs558549811	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75907724	AACATGGTGAAACCC[C/T]GTCTCCACTAAAAAA	26263
rs558643582	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915347	CACTGAAAGATTTTT[A/G]ATCTGAATTTGAGTC	26263
rs558729433	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75916186	AGTTAACCACTCTTA[C/T]GATGTTAACCTCTAT	26263
rs558859523	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934155	AATGGAATGTGAGGG[A/G]AAACGATTTTTTGTG	26263
rs558955757	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925511	GTGTGAAGAAGAACA[A/G]AGTTTTAAAATTATC	26263
rs559207436	in-del	-/AA	0.00398564	0.0444627	intron-variant	FBXO22	GRCh38.p7	15:75906919	AAATGCATTAATGAC[-/AA]GAGAAAATGTTGATT	26263
rs559275709	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902126	GAGGCTGGGGAGTTT[A/G]AAGAGTTAGCTGAGG	26263
rs559450750	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75906958	TGAAAACAGATTATG[A/G]AATTATATATTTAGT	26263
rs559456170	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75914604	TTTCTCTGCTTTGGT[A/G]CCACTCTTCAATGTT	26263
rs559737243	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75915667	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	26263
rs559798044	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932322	ATAGCAGAAGGCTTC[A/G]TTTAGTGGATATCTT	26263
rs559815775	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908644	CTCGAAGGTCAGGCA[C/G]GTAGCTGAAGAGGGT	26263
rs559845545	in-del	-/C	0.00438332	0.0466095	intron-variant	FBXO22	GRCh38.p7	15:75916901	AAAGTGTATTTACTA[-/C]CCCCCCAACTTTTTA	26263
rs559866219	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75916307	AATACCACAGACTGG[A/G]TGACTTAAACAACGG	26263
rs560004898	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912200	TGAGGATTTTCATAT[C/T]GATATTCAGGGATAT	26263
rs560026502	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924807	AGAGCCTCTTTGCTC[C/T]TTTGAGAATGCTTGA	26263
rs560045662	snp	C/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75912977	GTGTCCTTGTTCTCA[C/T]TGGTTTCAAAGAACC	26263
rs560091105	snp	C/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75923736	TGAACATGATAAATA[C/T]ATGCCTTTTAAATTT	26263
rs560152532	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75921384	CATTTTTGTTTGGCC[A/G]GGCACAGTGGCTCAT	26263
rs560168040	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75911564	GATTTGGCTTTCTGT[C/T]TGTCTGTTATTGGTG	26263
rs560176676	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75929057	TTCTGCACAGTTCAG[C/G]AGGCCAGAAGTCTGA	26263
rs560204888	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75924012	GTACCATTGACTAAG[A/G]TGAAGAAGATTTGAA	26263
rs560217377	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75921622	GCCAAGATTACACCA[C/G]TGCACTCCAGCCTGG	26263
rs560338533	snp	A/T	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918835	TGGCAGGCACCAGGA[A/T]CTGGGGTGGTTGGGA	26263
rs560400559	snp	A/G	0.00597247	0.0543191	intron-variant	FBXO22	GRCh38.p7	15:75904969	GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC	26263
rs560431434	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75927975	CTGGCAGAAGACATA[C/T]ATGCGGCCAACAATC	26263
rs560489508	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75908277	TTTTTGTTTTGTTTG[G/T]TTTTTTTTTTTTTTG	26263
rs560726059	snp	A/G			upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903816	GCTCCAGACGAGGGA[A/G]CGCACCGGCGTTGCC	26263
rs560840021	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905155	ATCCACATTTTCACT[A/G]TTAACAACAACGCTG	26263
rs560895903	snp	C/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75905749	CTTAGGAAAATCACA[C/G]GCTATTTTGTAGAAC	26263
rs560948857	snp	G/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913065	TCAGTTTCCATGTAG[G/T]TGTGTGGTTTTGAGT	26263
rs561006220	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75928469	CCATTATCATTAGCA[A/G]ACTAACACAGAAACA	26263
rs561113841	snp	A/G	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75920325	TTTGAGAACCATTTT[A/G]TGTGTTGCCTGGCAG	26263
rs561177138	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75919686	AGTGTTGGCCTCCAC[C/T]CTAGGCAGGCTTTAC	26263
rs561372478	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75924709	CCTGGCAGCTCTACC[G/T]GTCTGTACCACAGAC	26263
rs561408224	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	FBXO22	GRCh38.p7	15:75930460	CTGTGGAAATCTGGA[A/C]GGAGAATAGCATTAC	26263
rs561450413	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75926768	TGAGGTGAATGGTTA[C/T]ATTCCTGTGAGACTT	26263
rs561593459	snp	C/T			intron-variant	FBXO22	GRCh38.p7	15:75907240	TCAACCTCTCTGAGC[C/T]TCAGGTGCTATCTCC	26263
rs562097772	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903863	TCCAGCCGGAAGTGG[C/G]GCGGACGCCTGCTCA	26263
rs562385233	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75910511	ATTTGCATTTCTCTA[A/G]TGACTAGTAATGATG	26263
rs562450942	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75918798	TCTAAAAATGTTGCT[C/T]TCATAGAAATATAGA	26263
rs562648545	snp	A/T			intron-variant	FBXO22	GRCh38.p7	15:75917674	TGTTGATGATAAACT[A/T]GTTTGTATTTAGTTC	26263
rs562669258	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75934347	AACACCATAAGTGGC[A/G]TGGACTATCTACCTC	26263
rs562829178	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75912135	GCCGACTTGATTGTG[A/G]TAGATAAGCTTTTTG	26263
rs562866418	snp	G/T	0.000798403	0.0199641	intron-variant	FBXO22	GRCh38.p7	15:75904400	CCCGCAGGGATCTCC[G/T]GCTGCTGCGCCAGCG	26263
rs562950349	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B	FBXO22, FBXO22-AS1, NRG4	GRCh38.p7	15:75935115	TAGTAGTATTGATAA[A/G]AACAAAAGTCATCCT	26263
rs563093265	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75904175	CCAGGCTGGCGGGGT[G/T]GGGGGAGAGACCCTT	26263
rs563131280	snp	A/C	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75931564	TTGTTTTACTACTAG[A/C]TAGCCTTATTACTTT	26263
rs563328820	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932440	CAGAAATCGTTATGG[A/G]TGTGCATTGCCCCTT	26263
rs563493565	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903045	AGGACCGGGAATGTG[C/G]TAAAACTTAGTAGTT	26263
rs563494766	in-del	-/ATT	0.00597247	0.0543191	intron-variant, downstream-variant-500B	FBXO22, FBXO22-AS1	GRCh38.p7	15:75932233	ATAAAATCACCCTCC[-/ATT]ATTATATTTTTAATA	26263
rs563684313	snp	G/T			intron-variant	FBXO22	GRCh38.p7	15:75910812	GTTGCCATTGCTTTT[G/T]GTGTTTTAGTCATGA	26263
rs563780854	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925955	CAAAGACATCTCTTG[A/G]TGGACAACTACAGTA	26263
rs563844235	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	FBXO22, FBXO22-AS1	GRCh38.p7	15:75933229	GTAGCTTTGATTGAT[A/G]CTCTAAGATCACATG	26263
rs563916918	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917055	AAAAATTTCTTTCTG[A/G]ACCATTTGAAAGTTA	26263
rs563921118	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908671	GGGTCAGGTAGCTCA[A/G]TAGTCGTAGCACCAT	26263
rs563977411	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75924857	AACAGTTGACTCACA[C/T]CTGGGATCCTCCCTC	26263
rs564025026	snp	A/G	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75908531	CACCGTGGCCTCCCA[A/G]AGTGCTGATATTACA	26263
rs564031878	snp	A/G	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75925149	CCAGTTCTGGGGTGT[A/G]TATTTAATTTTACTT	26263
rs564063703	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75902025	GAAAGAACGCCCACT[A/T]TGAAAGGCAGTCAGG	26263
rs564098027	in-del	-/T			intron-variant	FBXO22	GRCh38.p7	15:75917227	GTTTAACTTTTTCTC[-/T]AGTGACTCCAATGGG	26263
rs564425360	in-del	-/AA	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75918836	GCAGGCACCAGGATC[-/AA]TGGGGTGGTTGGGAG	26263
rs564476087	snp	A/C	0.00119737	0.0244387	intron-variant	FBXO22	GRCh38.p7	15:75910380	CTAATTTGCACTCCT[A/C]CAAACAGTGTGAAAG	26263
rs564559996	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903125	CGTGCTTCACAGCAA[C/T]CATCTCACTCAGCTA	26263
rs564598501	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FBXO22	GRCh38.p7	15:75903796	GAGTACACCTCGGAG[G/T]ACGGGCTCCAGACGA	26263
rs564639674	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75917849	GAACAAGTAAAGTGA[C/T]CCTGATGAGTCTTAG	26263
rs564732860	snp	C/G			intron-variant	FBXO22	GRCh38.p7	15:75931591	CTTTAGTCACTTAAC[C/G]TTTTTGCGTCTTAGT	26263
rs564888398	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75908196	GTAAGAAACCTGAGG[C/T]CTAAAAGCTTGCTGA	26263
rs565004935	snp	A/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75920461	GGAAGGAAGAAGATG[A/T]TCAATGTGTTGATGT	26263
rs565124584	snp	C/T	0.000399281	0.0141238	intron-variant	FBXO22	GRCh38.p7	15:75913797	GTTATACTGCAATAT[C/T]AGCTGAACAGAAAGG	26263
rs565187549	snp	C/T	0.00199481	0.0315187	intron-variant	FBXO22	GRCh38.p7	15:75913102	CTTAATCCTGAGTTC[C/T]AATTTGATTGCACTA	26263
rs565193860	snp	C/T	0.00159617	0.0282053	intron-variant	FBXO22	GRCh38.p7	15:75921301	GAGTGAATGTGAAGG[C/T]CTAGCCCTGTATACT	26263
rs565345366	snp	A/G			intron-variant	FBXO22	GRCh38.p7	15:75907119	AGGCATGATTTTTCT[A/G]TAGCTTTAAGAGTTT	26263

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