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

RCBTB2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs10076	snp	C/T	0.167484	0.23599	intron-variant	RCBTB2	GRCh38.p7	13:48505367	ATGTATTTCTAGTGA[C/T]CAATTCAAATTAGTA	1102
rs11861	snp	C/G	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48505141	GCTGCGTGACTAGCA[C/G]TAGGCTGCGTGACTA	1102
rs751334	snp	A/G	0.0387552	0.1337	intron-variant	RCBTB2	GRCh38.p7	13:48506228	AGACCTGACAGGGAC[A/G]GAGGCCAACGCCGGG	1102
rs752663	snp	G/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534833	TAGACTAAAAATTTA[G/T]ACTCTGAGAGAGTAT	1102
rs877938	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48512678	TCAATAAGATTATGT[A/T]GACTTCTATAGTAGT	1102
rs877939	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48512677	CAATAAGATTATGTA[G/T]ACTTCTATAGTAGTC	1102
rs943278	snp	A/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48496038	AGACAACGTATAAGC[A/G]AGTATTTATATAATG	1102
rs943279	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48493315	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	1102
rs943281	snp	C/T	0.0402882	0.136092	intron-variant	RCBTB2	GRCh38.p7	13:48514153	aattgcaagcatcac[C/T]actcttgcactttgg	1102
rs943282	snp	C/T	0.0596104	0.162024	intron-variant	RCBTB2	GRCh38.p7	13:48517696	ATCTTTTCTGAATAA[C/T]CTTCATGGCACTATT	1102
rs943283	snp	C/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48517929	CGTCCAATGACTAGT[C/G]TCCTTAAAAGAAGAC	1102
rs943284	snp	A/G	0.48692	0.0798058	intron-variant	RCBTB2	GRCh38.p7	13:48517982	AGGGAAGAAGGCCAG[A/G]TGACAACAGACACAG	1102
rs977097	snp	C/G	0	0	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488811	GGAAAGCCCACCCTA[C/G]ACCACAAATAGCTGA	1102
rs2026580	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48495629	TAATATGTATTAAGC[A/C]CCTAAATTAAAGACA	1102
rs2148515	snp	A/G	0.296109	0.245711	intron-variant	RCBTB2	GRCh38.p7	13:48511279	ATAGCAGTTTTCCAT[A/G]TCATTAAAAATTCTT	1102
rs2274400	snp	C/G/T	0.0358264	0.128972	intron-variant	RCBTB2	GRCh38.p7	13:48521886	GCTCCAAGGGCATGA[C/G/T]TTTTTTCTAACCTTG	1102
rs2406934	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48493313	CACACACACACACAC[A/T]CACTCTCTCTCTCTC	1102
rs2897588	snp	C/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48514318	TGGTTCATGTCCCAG[C/G]TGGGATGGAGCAAGA	1102
rs3085589	in-del	-/AC	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48493259	cacacacacacacac[-/AC]tcttctctctctcac	1102
rs3085593	in-del	-/C/CTC/CTCTCTCC/CTCTCTCT/CTCTCTCTCC			intron-variant	RCBTB2	GRCh38.p7	13:48493341	tctctctctctctct[lengthTooLong]tctcttctctctctc	1102
rs3215827	in-del	-/T	0.4021	0.198407	intron-variant	RCBTB2	GRCh38.p7	13:48515485	ACCTAATTTCCATGC[-/T]TTTTTTTTTAACCTT	1102
rs3990837	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48495626	TATGTCTTTAATTTA[A/G]GGGCTTAATACATAT	1102
rs5803440	in-del	-/T			frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512802	TGTTTGTTTGACAGA[-/T]TAGTAGAGATATGAC	1102
rs6561447	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48508693	acaggcgtgagtgcc[C/T]ggccCATCCATGATT	1102
rs6561448	snp	C/T	0.397452	0.201886	intron-variant	RCBTB2	GRCh38.p7	13:48510190	AATAACCCTATCCTT[C/T]TCAACTGGCAAATTT	1102
rs6561449	snp	C/G	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48510222	CATGTAGCTGAGTGA[C/G]CAGCTTTATACCCCA	1102
rs6561450	snp	C/T	0.00713116	0.0592851	intron-variant	RCBTB2	GRCh38.p7	13:48511981	CTGATGTGGCAAACA[C/T]GGTTTTTAAACAAGA	1102
rs6561451	snp	C/G	0.00707995	0.0590749	intron-variant	RCBTB2	GRCh38.p7	13:48512206	TCAGTAAATGAAACA[C/G]ATTAATTTATAAACT	1102
rs6561452	snp	C/G	0.0295753	0.118402	intron-variant	RCBTB2	GRCh38.p7	13:48512462	TTTTCCAGCATTTGG[C/G]GATTTTTCTTATTGC	1102
rs6561453	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48512463	TTTCCAGCATTTGGG[A/G]ATTTTTCTTATTGCA	1102
rs6561454	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48512505	TACTACAGCAACAGA[A/G]AAGGAACAATACCTC	1102
rs6561455	snp	A/G	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48518349	AAGACCTTGCCCTAA[A/G]AAGGACACCTTCTGT	1102
rs6561456	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518472	GCAAAAAAAAAAAAa[A/T]atatatatatatata	1102
rs6561457	snp	C/G	0.397452	0.201886	intron-variant	RCBTB2	GRCh38.p7	13:48523751	CAGAAGGGAAATCTT[C/G]CTAATGTGCTAAAAT	1102
rs7316991	snp	A/T	0.116138	0.211142	intron-variant	RCBTB2	GRCh38.p7	13:48491429	TAAGCCCTCAGTGAT[A/T]AACAGGGAAAATTCA	1102
rs7317090	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513145	ATAAGTTTTTAATAA[A/G]GAGCAGAGAAAAGGC	1102
rs7319069	snp	C/T	0.135825	0.222405	intron-variant	RCBTB2	GRCh38.p7	13:48491688	GTGTCTGGAGTTAGG[C/T]GGCTGGGCAGTTTGA	1102
rs7319392	snp	A/T	0.444444	0.157135	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499144	cacacacacacacac[A/T]ctctctctctctctc	1102
rs7321483	snp	C/T	0.00723129	0.0596938	intron-variant	RCBTB2	GRCh38.p7	13:48496164	ATTTCTCCAGGAGGC[C/T]GGCAGCTGGAAGCAA	1102
rs7322110	snp	A/G	0.151001	0.229563	intron-variant	RCBTB2	GRCh38.p7	13:48513402	aaatataaccttata[A/G]tcaccccccaaaagg	1102
rs7322265	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513408	aaccttataatcacc[C/T]cccaaaaggccctca	1102
rs7322788	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48526175	CCTTTACCAAGGACA[C/T]GGAAATTCAATAAAC	1102
rs7322855	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513735	TTCAAATAAtaaata[C/T]agctgtcttataatt	1102
rs7323517	snp	C/T	0.116488	0.211364	intron-variant	RCBTB2	GRCh38.p7	13:48491188	TATGAACATTACACA[C/T]GATAGTCTTTTCTTC	1102
rs7324752	snp	C/T	0.116138	0.211142	intron-variant	RCBTB2	GRCh38.p7	13:48491123	CTCTCCAAGCTACTG[C/T]AGGTAATTTATAAAA	1102
rs7325162	snp	A/G	0.030278	0.119257	intron-variant	RCBTB2	GRCh38.p7	13:48531630	agagcaataaggcct[A/G]agtggtggaagtggg	1102
rs7325962	snp	C/T	0.406986	0.194565	intron-variant	RCBTB2	GRCh38.p7	13:48492967	attcaaaaccaaatt[C/T]ctgatatttccccca	1102
rs7326934	snp	C/G	0.364193	0.222396	intron-variant	RCBTB2	GRCh38.p7	13:48496376	GCATCCTGATTTACA[C/G]TTGCTCACTCAGCCA	1102
rs7330657	snp	A/G	0.0263992	0.111815	intron-variant	RCBTB2	GRCh38.p7	13:48523659	GAAGAAAGAGGGAGA[A/G]AAGAGAAAAAAGAAG	1102
rs7331860	snp	C/T	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48532814	CCCCGGAACCTAGCT[C/T]TTAACTCCCGCCAGC	1102
rs7332828	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48511713	GTTTTTAATACATTG[A/G]TATCTTTGCCAGCGA	1102
rs7332852	snp	C/T	0.0387552	0.1337	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501298	CTGTGCTAGCCTCAC[C/T]ATAGACCTTTTTGGT	1102
rs7333474	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48518474	AAAAAAAAAAAAAAA[A/T]ATATATATATATATA	1102
rs7334590	snp	G/T	0.00716407	0.0594198	synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511772	ACAGTGGACGTACCC[G/T]CTGGACACGGATGCC	1102
rs7981750	snp	C/T	0.143284	0.226079	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489785	CAGCCAGCTGAATAA[C/T]GGAACATTTGGGCCA	1102
rs7981773	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48519914	ctgagcatccctaat[C/T]caaaaatctgaatcc	1102
rs7984198	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48508010	TTCTGGGAAAGATTT[A/T]AAAAGGTTTCCCTTG	1102
rs7984309	snp	C/T	0.0825414	0.185628	intron-variant	RCBTB2	GRCh38.p7	13:48516516	tgtcttctccctatg[C/T]ctgttcacatcatct	1102
rs7984753	snp	G/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48508311	GAATACGCCCGTGAT[G/T]GAGTGCCTGGTTGAA	1102
rs7987935	snp	A/G	0.140919	0.224948	intron-variant	RCBTB2	GRCh38.p7	13:48529950	GACTGGAGTGCAATG[A/G]TGTGATCATGACTCA	1102
rs7987986	snp	C/T	0.0240643	0.107019	intron-variant	RCBTB2	GRCh38.p7	13:48530108	tttgccatgttgtcc[C/T]ggctggtctctaact	1102
rs7988584	snp	A/G/T	0.00874735	0.0655527	intron-variant	RCBTB2	GRCh38.p7	13:48508647	gacctcaggtgatcc[A/G/T]cccgccttggcctcc	1102
rs7988909	snp	C/T	0.00678886	0.0578648	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501702	AATATAATTGTTGAA[C/T]GAATTACTTTTCTCA	1102
rs7989808	snp	C/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48502197	TAAAATTAAAAAGCA[C/G]TCAAATAAGGATAgg	1102
rs7990414	snp	C/T	0.039522	0.134904	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517503	AAGTCCTCAAACTTT[C/T]AAGTTTCCTTCTGAT	1102
rs7995216	snp	A/G	0.197703	0.244469	intron-variant	RCBTB2	GRCh38.p7	13:48524200	GTTTGTGCACTACAC[A/G]TGGAGATTACCTTAC	1102
rs7996186	snp	C/G	0.0644693	0.167566	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533368	TCACCCCCACCTTCT[C/G]CAGGGTTATGTTCTC	1102
rs7997110	snp	C/T	0.228494	0.249073	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533105	GGCCCGGCGCCGCGA[C/T]GAGTTGGCGCCTCCC	1102
rs8001241	snp	A/G	0.397633	0.201754	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533517	GCCCCTCTATCTGGG[A/G]GCTCCGATCACTTCA	1102
rs8002023	snp	A/G	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48519549	CTGGGATTCCAATGC[A/G]TGTGTTTTCTTTAAT	1102
rs9316381	snp	A/G	0.327445	0.237702	intron-variant	RCBTB2	GRCh38.p7	13:48494283	ATTTGCCTGGCTCAA[A/G]TAAGCAAGAAATGGG	1102
rs9316382	snp	A/G	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48495279	ATGGTGGGATTGTGG[A/G]TGATTTTTATTTTCT	1102
rs9316383	in-del	-/AAGGA	0.364193	0.222396	intron-variant	RCBTB2	GRCh38.p7	13:48495987	AGAAGCCATAAAGGA[-/AAGGA]TTTATAGCTCTGATT	1102
rs9316384	snp	G/T	0.222035	0.248431	intron-variant	RCBTB2	GRCh38.p7	13:48500233	TCATATTGGATTAGG[G/T]CCCACCCTAGTGACC	1102
rs9316385	snp	C/T	0.397633	0.201754	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503605	GCCAAGATCCAAGAT[C/T]GTGCCACTGCACTCT	1102
rs9316386	snp	A/G	0.315273	0.241329	intron-variant	RCBTB2	GRCh38.p7	13:48505515	TTGTTGAAAAGAATG[A/G]TGCTGATTGAGAAGC	1102
rs9316387	snp	G/T	0.222333	0.248464	intron-variant	RCBTB2	GRCh38.p7	13:48514287	TCCCTTTGTCCAGCA[G/T]CTCTGCCATAGACAC	1102
rs9316388	snp	A/G	0.32768	0.237625	intron-variant	RCBTB2	GRCh38.p7	13:48515087	TATGTTTTGGATACC[A/G]TAAAACATGAATGTA	1102
rs9316389	snp	A/G	0.0948562	0.196037	intron-variant	RCBTB2	GRCh38.p7	13:48517011	CCAGACCACATTCCC[A/G]GTAAGGTTGATTTAA	1102
rs9316390	snp	G/T	0.0955749	0.196603	intron-variant	RCBTB2	GRCh38.p7	13:48517783	gccattcaacccaCT[G/T]CAGCTCCTCTCTGGG	1102
rs9316391	snp	A/G	0.095934	0.196885	intron-variant	RCBTB2	GRCh38.p7	13:48517978	gtctgttgtcatctg[A/G]ccttcttccctgtgc	1102
rs9316392	snp	A/G	0.166832	0.235761	intron-variant	RCBTB2	GRCh38.p7	13:48519447	ATCATTTGTAGACAG[A/G]TATGTAAGAGCTGGC	1102
rs9316393	snp	C/T	0.328148	0.237472	intron-variant	RCBTB2	GRCh38.p7	13:48520790	TTAAATATACTGTAT[C/T]TTAAATTGAATTGCA	1102
rs9316394	snp	C/T	0.499218	0.0197529	intron-variant	RCBTB2	GRCh38.p7	13:48526428	GTAGTCCCAGCTACT[C/T]GGGAGGCTAAGATAG	1102
rs9316395	snp	A/T	0.49925	0.0193545	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533826	TGAGTGGGTTTTGGT[A/T]AAATGCTCAACAATT	1102
rs9316396	snp	A/G	0.335559	0.234904	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533874	CCTGTGAAGTAAGCT[A/G]CTTGCTTTTATACTG	1102
rs9331951	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48524935	TTACATTTTATAACT[C/T]TAGTATTTTTATAAT	1102
rs9331952	snp	A/G	0.0127383	0.0787839	intron-variant	RCBTB2	GRCh38.p7	13:48524640	CAAAAGTTTTTGGAG[A/G]GAATGCTCCCAGCCA	1102
rs9331953	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48524442	TGAATAAAATGGAGG[C/G]AATGATTAacctgtt	1102
rs9331954	snp	C/T	0.0244538	0.107838	intron-variant	RCBTB2	GRCh38.p7	13:48524431	GAGGCAATGATTAac[C/T]tgtttcatttggata	1102
rs9331955	snp	A/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48524144	TTTTCTTTATTATGT[A/T]TGCATCACATTGAAA	1102
rs9331956	snp	A/G	0.0341408	0.126114	intron-variant	RCBTB2	GRCh38.p7	13:48523968	CTTACATTTCATTCA[A/G]TTTGAATCCTGCATG	1102
rs9331957	snp	C/T	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48523918	AATTTCCATGACATA[C/T]ATACAATTATGTCTT	1102
rs9331958	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48523777	CAAAAGCCCAGGATC[A/G]GTTTTTCATGATTTT	1102
rs9331959	snp	C/G	0.0644693	0.167566	intron-variant	RCBTB2	GRCh38.p7	13:48523651	TTCTCTTCTCTCCCT[C/G]TTTCTTCTCCTCTCC	1102
rs9331960	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48523617	tattttttattcCAG[C/T]AAACTTGGGGCAAAT	1102
rs9331961	snp	C/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48523606	cCAGTAAACTTGGGG[C/T]AAATATGGAAAAAGT	1102
rs9331962	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48523582	AAAAAGTGTTTCCTG[A/G]TAGGGTGAGGCAGAA	1102
rs9331963	snp	C/T	0.0228947	0.104514	intron-variant	RCBTB2	GRCh38.p7	13:48523451	TGTGGGTTATAGCAA[C/T]GAAGGAATCGTCTGC	1102
rs9331964	snp	G/T	0.00398564	0.0444627	intron-variant	RCBTB2	GRCh38.p7	13:48523062	ATATCTTTTTTACTT[G/T]TTTCCAAATGTTAGA	1102
rs9331965	snp	A/G	0.0652144	0.168387	intron-variant	RCBTB2	GRCh38.p7	13:48522978	AAATTATGATTTCTC[A/G]TATTCTGAGAGATCT	1102
rs9331966	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48522733	TAGAAAAAGCAACAT[C/G]ATTAAATACAGCCTT	1102
rs9331967	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48522106	GCTGTTCATTCCCAT[A/G]CCTAAAGCTTAATTC	1102
rs9331968	snp	A/T	0.0112836	0.0742604	intron-variant	RCBTB2	GRCh38.p7	13:48521887	GCAAGGTTAGAAAAA[A/T]ATCATGCCCTTGGAG	1102
rs9331969	snp	A/T	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48521060	TAAAATAAAGAATAG[A/T]TTCACAGAATCAGCA	1102
rs9331970	snp	A/G	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48520976	acaaagtgttataat[A/G]aatgaatatgatata	1102
rs9331971	snp	A/G	0.0197866	0.0976138	intron-variant	RCBTB2	GRCh38.p7	13:48520821	CTAGGTATGCCTAAC[A/G]TAATTTTGATTCTCT	1102
rs9331972	snp	C/T	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48520238	AGATTGAGGCTCCTA[C/T]GGGGGACTATTGTGT	1102
rs9331973	snp	A/G	0.0644693	0.167566	intron-variant	RCBTB2	GRCh38.p7	13:48519825	TCAGTTCCCTATGTA[A/G]TAGTTGCCCTAACAA	1102
rs9331974	snp	A/G	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48519434	AGGTATGTAAGAGCT[A/G]GCTGGAATTTACAGC	1102
rs9331975	snp	A/G	0.0399052	0.1355	intron-variant	RCBTB2	GRCh38.p7	13:48519328	AAAAATGAAATAGCC[A/G]TCAGTCATTGTATCT	1102
rs9331976	snp	C/G	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48519289	GTGCTGTTTGTGGAA[C/G]ACAACCCACAGTAGG	1102
rs9331977	snp	C/T	0.0260105	0.111035	intron-variant	RCBTB2	GRCh38.p7	13:48519097	agaagctagtgatct[C/T]gaaagattacttagt	1102
rs9331978	snp	G/T	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48519082	TGAAAGATTACTTAG[G/T]CTCCCTGTGCCCCAG	1102
rs9331979	snp	C/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48518209	AGCTGCTTGTCTTCt[C/T]tgttagtttctttgt	1102
rs9331980	snp	C/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48518173	tgtaacaaatgacta[C/T]aattcaaacaacaga	1102
rs9331981	snp	C/T	0.0349115	0.127424	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517399	TTGGGGCCCAGTTTT[C/T]GGAATGGCTTCCGTG	1102
rs9331982	snp	C/T	0.0263992	0.111815	intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517394	GCCCAGTTTTCGGAA[C/T]GGCTTCCGTGTGAAG	1102
rs9331983	snp	A/C	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48516894	TGCCATTTGATAGAC[A/C]TATTGGCTGTTTATG	1102
rs9331984	snp	A/G	0.0678174	0.1712	intron-variant	RCBTB2	GRCh38.p7	13:48516789	GGTAAAACTCTTTCA[A/G]ACAAATTTATAACTT	1102
rs9331985	snp	A/G	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48516780	CTTTCAAACAAATTT[A/G]TAACTTCCTCTTATA	1102
rs9331986	snp	C/G/T	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48516770	AATTTATAACTTCCT[C/G/T]TTATAGGAGTGTGGG	1102
rs9331987	snp	C/T	0.00332778	0.0406548	intron-variant	RCBTB2	GRCh38.p7	13:48516698	accctgcaacattta[C/T]gtgttgaagtacagc	1102
rs9331988	snp	A/G	0.0573587	0.15934	intron-variant	RCBTB2	GRCh38.p7	13:48515931	TCCATCCGGGCCTCC[A/G]CTGCTCGATGGCTGT	1102
rs9331989	snp	C/T	0.00780038	0.0619625	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515263	GGATTCTTTAAATGG[C/T]AAAAAAATAGCCTGC	1102
rs9331990	snp	A/T	0.00051257	0.0160007	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515209	TATTGTCCTTGCAAC[A/T]ACAGGTAACCTAGGA	1102
rs9331991	snp	A/G	0.195214	0.243923	intron-variant	RCBTB2	GRCh38.p7	13:48515053	GAATGCCAGCATAAG[A/G]TGATGTGGCAGATGG	1102
rs9331992	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48515013	ATCATTGGCATTTTA[A/G]ATGTATGAATGACAA	1102
rs9331993	snp	A/G	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48514974	GCCCAGTAAACACTG[A/G]CGaactgattgtgga	1102
rs9331994	snp	A/G	0.0693013	0.172766	intron-variant	RCBTB2	GRCh38.p7	13:48514972	CCAGTAAACACTGAC[A/G]AACTGATTGTGGACT	1102
rs9331995	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48514938	gcaagtctgtctgaa[C/T]tttggattcttgatc	1102
rs9331996	in-del	-/T	0.0689305	0.172377	intron-variant	RCBTB2	GRCh38.p7	13:48514850	CTGTGATTCTTACAC[-/T]TAAAGAGTGACTGAT	1102
rs9331997	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48514304	agctgggacatgaac[C/T]atccctttgtccagc	1102
rs9331998	snp	A/G	0.0948562	0.196037	intron-variant	RCBTB2	GRCh38.p7	13:48514288	atccctttgtccagc[A/G]tctctgccatagaca	1102
rs9331999	snp	A/G	0.00636936	0.0560724	intron-variant	RCBTB2	GRCh38.p7	13:48511651	TGCTTGGATGTCTTC[A/G]TTAAAGTAAAGGTTA	1102
rs9332000	snp	A/G	0.000429376	0.0146459	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510768	TTTTCCTTCCAGGTC[A/G]CCTGTGGCTACGCAC	1102
rs9332001	snp	C/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48510559	CAGGACTTAGATATA[C/T]AGAGAATGGTGGGGA	1102
rs9332002	snp	A/G	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48510270	ATAACATTCAAGGTC[A/G]CTCTTCCCTGGCTTA	1102
rs9332003	snp	A/G	0.0399052	0.1355	intron-variant	RCBTB2	GRCh38.p7	13:48510131	ACGAGGAAGAGTAAA[A/G]TGGTTAGGAAATTAA	1102
rs9332004	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48509995	AAGCATGGTCAGATC[A/G]CTGCCTTTCCACTTT	1102
rs9332005	snp	C/T	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48509979	CTGCCTTTCCACTTT[C/T]CATTTCCTGATAGTA	1102
rs9332006	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48509967	TTTTCATTTCCTGAT[A/G]GTAGTGTAGAGCAAA	1102
rs9332007	snp	A/G	0.00687277	0.0582164	intron-variant	RCBTB2	GRCh38.p7	13:48509579	GCCCCTTCAGAATTG[A/G]GAGGAGGGACAATAA	1102
rs9332008	snp	C/T	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48509569	AATTGGGAGGAGGGA[C/T]AATAATGGAGGCAGG	1102
rs9332009	snp	A/G	0.0399052	0.1355	intron-variant	RCBTB2	GRCh38.p7	13:48509560	GAGGGACAATAATGG[A/G]GGCAGGAGGTGGTGC	1102
rs9332010	snp	A/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48509456	AGGCTTTGAATAACC[A/T]CAAAAGTGCCTCAGT	1102
rs9332011	snp	A/G	0.0256215	0.110247	intron-variant	RCBTB2	GRCh38.p7	13:48508649	tgggaggccaaggcg[A/G]gcggatcacctgagg	1102
rs9332012	snp	A/G	0.00341879	0.0412033	intron-variant	RCBTB2	GRCh38.p7	13:48508052	GAGAAATCTGTCTAC[A/G]TTGTTTTCTTTGCTG	1102
rs9332013	snp	A/C	0.0244538	0.107838	intron-variant	RCBTB2	GRCh38.p7	13:48508007	GGGAAACCTTTTAAA[A/C]TCTTTCCCAGAAAAA	1102
rs9332014	snp	C/T	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48507865	CTGAAGTTTCAGTAC[C/T]TTGGGGACAGATTGA	1102
rs9332015	snp	C/T	0.0611083	0.163768	intron-variant	RCBTB2	GRCh38.p7	13:48507753	TTTCTGAGAATTCTT[C/T]GACTTCTGAGGTAGT	1102
rs9332016	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48507748	GAGAATTCTTTGACT[C/T]CTGAGGTAGTTGGTA	1102
rs9332017	snp	C/T	0.00356505	0.0420692	intron-variant	RCBTB2	GRCh38.p7	13:48507558	CTAGTACTTCATAGC[C/T]AATAAGCTCAGCAGT	1102
rs9332018	snp	C/T	0.0391387	0.134304	intron-variant	RCBTB2	GRCh38.p7	13:48507402	GGTTAGCTCAGTTGA[C/T]AGTCATTGTCTGTCG	1102
rs9332019	snp	A/G	0.0267878	0.112589	intron-variant	RCBTB2	GRCh38.p7	13:48507270	TTGCTTGGGTCACAA[A/G]CCTAGACCTGAAAGT	1102
rs9332020	snp	C/T	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48507255	GCCTAGACCTGAAAG[C/T]ACCCTCTAAACTTTC	1102
rs9332021	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48507126	GGCCATGCCCCGGGA[C/T]GGGCAGCATCACATG	1102
rs9332022	snp	C/G	0.0539704	0.155153	intron-variant	RCBTB2	GRCh38.p7	13:48506928	GCTTTTCTGATGTTG[C/G]GCAGATCAGTGAAGG	1102
rs9332023	snp	A/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48506833	TTCCAAAAAATGTAG[A/G]AGTCTTTGCCTAGTA	1102
rs9332024	snp	A/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48506816	GTCTTTGCCTAGTAG[A/G]TCACTGCAAAGTGCT	1102
rs9332025	snp	A/G	0.095934	0.196885	intron-variant	RCBTB2	GRCh38.p7	13:48506240	TTGCCCTCCGATCCC[A/G]GCGTTGGCCTCCGTC	1102
rs9332026	snp	C/T	0.0112991	0.0743093	intron-variant	RCBTB2	GRCh38.p7	13:48506222	GTTGGCCTCCGTCCC[C/T]GTCAGGTCTTGTACG	1102
rs9332027	snp	C/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48506198	TTGTACGATGCTGCT[C/G]TCTGCCATCCTGCCG	1102
rs9332028	snp	A/G	0.0146672	0.084371	intron-variant	RCBTB2	GRCh38.p7	13:48506183	CTCTGCCATCCTGCC[A/G]TCTCCAGCTCTGCCT	1102
rs9332029	snp	G/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48505981	CATTTGGGAATTATT[G/T]GCAAAGTCACAGATC	1102
rs9332030	snp	A/G	0.0238061	0.106472	intron-variant	RCBTB2	GRCh38.p7	13:48505930	AATCATGAGTTCCTC[A/G]GCTAAATCACGGGCC	1102
rs9332031	snp	G/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48505802	CACAAACCGTGAGAG[G/T]ATTGCTGCCTGTATC	1102
rs9332032	snp	C/T	0.0322114	0.122752	intron-variant	RCBTB2	GRCh38.p7	13:48505648	CACGAAGACAGACCA[C/T]GTCGCTATCCTCACA	1102
rs9332033	snp	A/G	0.0681886	0.171594	intron-variant	RCBTB2	GRCh38.p7	13:48504856	GCCGGTACAAGCTCC[A/G]GGTTCTGTGATAACA	1102
rs9332034	snp	A/G	0.0425829	0.139564	intron-variant	RCBTB2	GRCh38.p7	13:48504777	CATCCTCACCCTTCA[A/G]GTGCTAGCCCGTGTC	1102
rs9332035	snp	A/C	0.0154538	0.0865337	intron-variant	RCBTB2	GRCh38.p7	13:48504589	TGAAACGGATGCATA[A/C]AGTAACAGGGCCAGG	1102
rs9332036	snp	A/G	0.153	0.230415	intron-variant	RCBTB2	GRCh38.p7	13:48504535	GCTGCAGGAGCTCAG[A/G]TGAGCGGGAGACCTC	1102
rs9332037	snp	C/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48504500	TTGGGGCAGTTTGAA[C/T]TGGGCCTTACAAGAT	1102
rs9332038	snp	G/T	0.0611083	0.163768	intron-variant	RCBTB2	GRCh38.p7	13:48504419	TGAAGTCATTGAAGG[G/T]CAATGAGAAAGCCTG	1102
rs9332039	snp	A/G	0.0232847	0.105357	intron-variant, synonymous-codon, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504387	TTGTTGAAACAGGGT[A/G]TGTGGACAAAATTGA	1102
rs9332040	snp	A/G	0.00344233	0.0413439	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503875	CCAGATCAACAAGAC[A/G]ATGTTTTCCATTAAG	1102
rs9332041	snp	C/T	0.0232847	0.105357	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503792	ggaggccaaggtggg[C/T]ggatcatttgagctc	1102
rs9332042	snp	G/T	0.0154538	0.0865337	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503663	tactacagaggctga[G/T]gtaggaggatcgctt	1102
rs9332043	in-del	-/T	0.484763	0.0859435	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502952	ACTTGTTTCTGCCCC[-/T]GGTCACTGTGCTTAT	1102
rs9332044	snp	A/C	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48502132	TTACTCAAATGTTTA[A/C]AATTTCATGCAAAAT	1102
rs9332045	snp	A/C	0.00410503	0.0451183	intron-variant	RCBTB2	GRCh38.p7	13:48501875	AGCATTTGCATTATT[A/C]TCCTAGAACCTGATG	1102
rs9332046	snp	A/G	0.00353981	0.0419211	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501649	CACCTCAGTAATCAA[A/G]AAAAATTGTAAGGCT	1102
rs9332047	snp	C/T	0.0232847	0.105357	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501592	GAGCGGGGAGAAATA[C/T]ACATGAAACAAGAAA	1102
rs9332048	snp	C/T	0.0252325	0.109451	intron-variant	RCBTB2	GRCh38.p7	13:48500977	AAATTCATTATGTTG[C/T]TGTGTAACAGATATT	1102
rs9332049	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48500836	CCTGCATGAAAGAAG[C/G]GGGGTGGATTTGTTt	1102
rs9332050	snp	C/T	0.166832	0.235761	intron-variant	RCBTB2	GRCh38.p7	13:48500421	acaggcgcacaccac[C/T]atgcctggctaattt	1102
rs9332051	snp	C/T	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48500402	cctggctaatttttg[C/T]atttttagtagagat	1102
rs9332052	snp	A/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48500375	agatggggtttcacc[A/G]tattggccaggctgg	1102
rs9332053	snp	C/T	0.151334	0.229706	intron-variant	RCBTB2	GRCh38.p7	13:48498429	GTGGCAGTTTTTTAT[C/T]ggcccaccactaaca	1102
rs9332054	snp	A/G	0.0368636	0.130663	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496209	TCTGCTCTCGGCTGC[A/G]GTGAAGTATGATGCA	1102
rs9332055	snp	A/G	0.0916144	0.193427	intron-variant	RCBTB2	GRCh38.p7	13:48495623	GTATTAAGCACCTTA[A/G]ATTAAAGACATAATT	1102
rs9332056	in-del	-/GT	0.364401	0.222289	intron-variant	RCBTB2	GRCh38.p7	13:48495402	ACTAAGTGAAAAACT[-/GT]TATCCTATTTTTATT	1102
rs9332057	snp	A/G	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48495076	GACATTTTAGTAGAT[A/G]AAAGGTTATAACTTT	1102
rs9332058	in-del	-/A	0.0748431	0.178382	intron-variant	RCBTB2	GRCh38.p7	13:48494659	GCACGTGGTGTTTGC[-/A]ATCTGAATCAGGCTT	1102
rs9332059	snp	A/G	0.0126979	0.078662	intron-variant	RCBTB2	GRCh38.p7	13:48494324	AAAATACAAGCTTTC[A/G]TAAATAAAGAACAGT	1102
rs9332060	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48494303	AAAGAACAGTGCTGT[A/G]TTTGATTTGCCTGGC	1102
rs9332061	snp	A/G	0.00340715	0.0411335	intron-variant	RCBTB2	GRCh38.p7	13:48493995	TAACTACAATTCTCC[A/G]TTGTCCTCAGTATTT	1102
rs9332062	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48491604	CAGCCAAAGAGATGA[C/T]GCATCTCTATCTGGT	1102
rs9332063	snp	C/T	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48491508	AAATGGACTCTGAGA[C/T]ATTCAGCATGTATCA	1102
rs9332064	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48491400	TACCTGGGACAGAGA[C/T]ACATCATATTGCTGG	1102
rs9332065	in-del	-/GAAAA	0.131723	0.220251	intron-variant	RCBTB2	GRCh38.p7	13:48491300	TTTCTTTTCTTAAAA[-/GAAAA]TGTACCGTAGGTTTA	1102
rs9332066	snp	G/T	0.184838	0.241358	intron-variant	RCBTB2	GRCh38.p7	13:48490830	GATTTCTTTAAAGCA[G/T]TTTCCCAGTTGAGAT	1102
rs9332067	snp	A/G	0.00336134	0.0408579	intron-variant	RCBTB2	GRCh38.p7	13:48490767	TCCATCCCATCCTGT[A/G]TCGTCTCATAAAGAG	1102
rs9332068	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48490764	ATCCCATCCTGTGTC[A/G]TCTCATAAAGAGAAA	1102
rs9332069	in-del	-/TG	0.0115603	0.0751433	intron-variant	RCBTB2	GRCh38.p7	13:48490742	AAAGAGAAAAAGCGG[-/TG]TGGCCTGTTAATGAC	1102
rs9332070	snp	C/T	0.0391387	0.134304	intron-variant	RCBTB2	GRCh38.p7	13:48490710	CAGAGCAGCAATTTC[C/T]TGGCATTACTGCTTT	1102
rs9332071	snp	A/G	0.0130921	0.0798413	intron-variant	RCBTB2	GRCh38.p7	13:48490672	TTACCTTTTTCTTCC[A/G]TCAACTCTTTATAGG	1102
rs9332072	snp	C/T	0.0154538	0.0865337	intron-variant	RCBTB2	GRCh38.p7	13:48490566	AACAGTTACAAATAC[C/T]GTCACTAGACAAAGG	1102
rs9332073	snp	A/G	0.0119091	0.0762411	intron-variant	RCBTB2	GRCh38.p7	13:48490433	TAAATTTTTACAAGC[A/G]TAGATGATTCATACT	1102
rs9332074	snp	C/G	0.0228947	0.104514	intron-variant	RCBTB2	GRCh38.p7	13:48490378	TTAGGTATTACCATG[C/G]CATCATTTCCTCCAC	1102
rs9332075	snp	C/G	1.64868e-05	0.00287109	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490223	TCTGCTTCAGGTTTT[C/G]CATAAACCATCTGAC	1102
rs9332076	snp	A/C/G	0.00174526	0.0294894	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490085	AGGAAAGTTTTTGAG[A/C/G]CTTTCCATTTCCCCT	1102
rs9332077	snp	C/T	0.0228947	0.104514	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489954	GTGGTCTTTGTCTGC[C/T]TAAACCCAGAGTTTA	1102
rs9332078	snp	A/C	0.0154538	0.0865337	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489744	GATAGCTTgacaagg[A/C]gtgctgtctgtcctt	1102
rs9332079	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489738	TTgacaaggagtgct[A/G]tctgtccttaccaca	1102
rs9332080	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489575	CAGCCTGTAATTATT[A/G]AGGTTCATATTCTTC	1102
rs9332081	snp	C/T	0.0228947	0.104514	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489212	AGTATAACTATAAAG[C/T]ACTAGCTGAGAAGGA	1102
rs9332082	snp	C/G	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489185	AGGAACTGATACTTA[C/G]ATTTCATGGACAGCA	1102
rs9332083	snp	A/T	0.00335007	0.0407899	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489124	TAGATCAAAACAAAT[A/T]ACCTAATTGCAAAAG	1102
rs9332084	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489020	CCTTTTGGAATTAGA[A/G]TTCTTGTTCTGATGC	1102
rs9332085	snp	C/T	0.0399052	0.1355	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488854	ATATTATGCTCTTAT[C/T]AAGCAGTTACTCGGA	1102
rs9332086	snp	C/T	0.115438	0.210697	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488752	TGTCTTGGTCTGCTC[C/T]TTATTGGTGAGGTGA	1102
rs9332087	snp	C/T	0.02016	0.0983543	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488736	TTATTGGTGAGGTGA[C/T]Ttttttgaagactat	1102
rs9535035	snp	A/G	0.499203	0.0199521	intron-variant	RCBTB2	GRCh38.p7	13:48497927	TCTGCCCCAAGCCCC[A/G]GCTCTGCGCCTCCTC	1102
rs9568046	snp	A/T	0.375	0.216506	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499146	CACACACACACACTC[A/T]CTCTCTCTCTCTCTC	1102
rs9591167	snp	G/T	0.152001	0.229992	intron-variant	RCBTB2	GRCh38.p7	13:48518698	AATTGAGGAATCCAA[G/T]AATCTTTATTTAAAA	1102
rs9591168	snp	C/T	0.0197687	0.0974348	intron-variant	RCBTB2	GRCh38.p7	13:48528376	AGATCAACTCTAAAG[C/T]TATGCTTGAGAAACA	1102
rs9591169	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48530733	TACATAGATGTCTGG[C/T]TAGCTCTTCCTTGTA	1102
rs9591170	snp	C/T	0.152001	0.229992	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533657	TTGGGGCCAAGGGCT[C/T]CGAAAACAGCCACCT	1102
rs9591171	snp	C/T	0.163236	0.234461	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534918	acatctgtacctgtg[C/T]actctattccttccc	1102
rs9595913	snp	A/C	0.16618	0.23553	intron-variant	RCBTB2	GRCh38.p7	13:48514462	cttgagaaagtaaaa[A/C]caaggataacgggag	1102
rs9595914	snp	C/T	0.223225	0.248562	intron-variant	RCBTB2	GRCh38.p7	13:48518536	CACAGGCATTTCCTA[C/T]AGGACAACCTTAATT	1102
rs9595915	snp	A/G	0.0182019	0.0936463	intron-variant	RCBTB2	GRCh38.p7	13:48526643	aaaTAGCctgggcgc[A/G]gtggctcatgcctgt	1102
rs9595916	snp	A/C/G			intron-variant	RCBTB2	GRCh38.p7	13:48527352	GATATATATATATAT[A/C/G]ATATATATTTATATA	1102
rs9595917	snp	C/T	0.152334	0.230133	intron-variant	RCBTB2	GRCh38.p7	13:48529978	tcactgcagcctcaa[C/T]cttcccggctccagt	1102
rs10129123	snp	A/G	0.0111196	0.0737302	intron-variant	RCBTB2	GRCh38.p7	13:48530236	CAAGTAAACCTCAAC[A/G]GTAGCAGTATCTTGG	1102
rs10567858	in-del	-/GAGA			intron-variant	RCBTB2	GRCh38.p7	13:48516108	AGACAGAGAGAGAGA[-/GAGA]GAGAGAGAGCTGCCA	1102
rs10680748	in-del	-/AC	0.296619	0.245615	intron-variant	RCBTB2	GRCh38.p7	13:48502169	AGTTAAAAGTAAAAA[-/AC]ACAGTTTCTCAGTAA	1102
rs10691494	in-del	-/CCTTT/TCCTT			intron-variant	RCBTB2	GRCh38.p7	13:48495988	AGCTATAAATCCTTT[-/CCTTT/TCCTT]ATGGCTTCTGCCTTT	1102
rs11617029	snp	G/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48491873	TTCCTGTGATTCTAA[G/T]AATTCAATAAATTGG	1102
rs11839027	snp	G/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48517676	AGCTTTGTTTTCAGG[G/T]TTCTATCTTTTCTGA	1102
rs12584452	snp	C/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48522000	AATCAGGATCCCTTA[C/T]GTTCGATGGAACCAG	1102
rs12585384	snp	A/G	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48528798	GACAAGTAACAGTAA[A/G]ATACCTACATGGCTA	1102
rs12857866	snp	A/G	0.067446	0.170804	intron-variant	RCBTB2	GRCh38.p7	13:48532144	TTATGTAATTTTTGC[A/G]AAGAACAAAAGCAAA	1102
rs12867099	snp	A/C	0	0	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502993	TCCCGCCAGGTTTAA[A/C]TGATGTGGGACATCA	1102
rs12867263	snp	G/T	0	0	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515661	ACGAATTAACTGTAG[G/T]TCTTCTTCAGAACAA	1102
rs12872844	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48527329	TTGGCTCatatatat[A/T]tatatatgatatata	1102
rs12874121	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48527391	atatatgatatatat[A/T]tatatTAAAAGGTGC	1102
rs17071843	snp	A/G	0.0611083	0.163768	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503532	ATTGATGAGGAGGTA[A/G]TTCTCAGAACAATTT	1102
rs34008611	in-del	-/C			intron-variant	RCBTB2	GRCh38.p7	13:48532884	GGTCGCGGCTCTAGT[-/C]CCCTGGGCCCCTCAG	1102
rs34188167	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48522199	TCCTGCTGAGGTCTG[-/A]AAAAGTAGTCTCAAA	1102
rs34271504	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48504493	CTACCCATCTTGTAA[-/G]GGCCCAGTTCAAACT	1102
rs34418781	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48526938	ATAATAATAAATAGA[-/T]TTTTTTTTAAATAGG	1102
rs34538329	in-del	-/C			intron-variant	RCBTB2	GRCh38.p7	13:48494996	ATGAGTCATTACCTT[-/C]CCTCACTTTTTGTCT	1102
rs34686966	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48508199	CTCCGGGGTTCCCCA[-/G]GGGATAAGTTATGAC	1102
rs34823603	in-del	-/T			frameshift-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490193	CTGCAAAACCTGATG[-/T]TTTGTGTTACTACAG	1102
rs35061928	multinucleotide-polymorphism	AA/CT			intron-variant	RCBTB2	GRCh38.p7	13:48512677	GACTACTATAGAAGT[AA/CT]ACATAATCTTATTGA	1102
rs35285230	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48506066	GCTCCTCAGGGAATA[-/T]TTTCAAGTAAAAGGG	1102
rs35294270	in-del	-/CA			intron-variant	RCBTB2	GRCh38.p7	13:48502170	TAAAAGTAAAAAACA[-/CA]GTTTCTCAGTAAAAT	1102
rs35298504	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489139	AATTTGTTTTGATCT[-/A]AAAAGTACAAATTTA	1102
rs35472352	in-del	-/C			utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48524720	CTGTTCCTTTTAGAT[-/C]CCTTGTAAAGTTGTC	1102
rs35653432	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48506360	TTTGTAAACAGGGCC[-/A]TGATGTGAGGAAATG	1102
rs35697351	in-del	-/CA			intron-variant	RCBTB2	GRCh38.p7	13:48493226	CTAAGTACCCTCCTT[-/CA]CACACACACACACAC	1102
rs35774425	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48497876	GGCCCCAAGCTTCAG[-/A]ACACACATGCAAGCT	1102
rs35929216	in-del	-/C	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48521657	TTGCGCCTCATCTGT[-/C]ACTGTCACCATCGCT	1102
rs36044425	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48504552	GAGCTCCTGCAGCAC[-/T]TTCCTGTCCACACCA	1102
rs36115156	in-del	-/G			intron-variant	RCBTB2	GRCh38.p7	13:48491436	CAGTGATAAACAGGG[-/G]AAAATTCACACACCC	1102
rs41284770	snp	A/G	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48490517	AACTTTTTCTTCCCA[A/G]AGATAGGCATGTGAG	1102
rs41284772	snp	G/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48515848	TTGGGAGGAACACAC[G/T]GCATCCATTTTTGAG	1102
rs41290412	snp	A/G/T	6.59783e-05	0.00574324	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502818	GTGCGGGAGGATCAC[A/G/T]GACTGACCCCGGCAC	1102
rs55686933	snp	A/G	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48514191	ATTAAGTAAAATAAG[A/G]GTGACTTGAACACAA	1102
rs55839837	snp	A/C	0.089084	0.191327	intron-variant	RCBTB2	GRCh38.p7	13:48528448	TTAAAATTATCCCAT[A/C]TGGGTGGGTAACACA	1102
rs56111734	snp	C/T			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489372	TTATGTAAGGCAGAT[C/T]AGCCCAGGAATTTCA	1102
rs56155028	snp	A/G	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48529557	AGCAAGGCTGAAGAC[A/G]TAAAAGAAACCCACT	1102
rs56318255	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490379	TGGAGGAAATGATGG[C/T]ATGGTAATACCTAAA	1102
rs57026972	snp	A/C/G	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48528131	AAAGCAAATACATGA[A/C/G]AGCAAACAGAATAAC	1102
rs57910291	snp	C/T	0.0279526	0.114869	intron-variant	RCBTB2	GRCh38.p7	13:48529938	CACTATTGCCCAGAC[C/T]GGAGTGCAATGGTGT	1102
rs58227630	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508650	CTCAGGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	1102
rs58286186	in-del	-/CA	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48495403	ATAAAAATAGGATAA[-/CA]GTTTTTCACTTAGTG	1102
rs58426997	in-del	-/AC			intron-variant	RCBTB2	GRCh38.p7	13:48493260	CACACACACACACAC[-/AC]TCTTCTCTCTCTCAC	1102
rs58455074	in-del	-/AAAAA			intron-variant	RCBTB2	GRCh38.p7	13:48518469	TTTGCAAAAAAAAAA[-/AAAAA]TATATATATATATAT	1102
rs59350616	in-del	-/AT			intron-variant	RCBTB2	GRCh38.p7	13:48525418	TATATATATATATAT[-/AT]TCAGTTATATATGTA	1102
rs60410511	snp	A/G	0.00737801	0.0602874	intron-variant	RCBTB2	GRCh38.p7	13:48510808	CAGGACTGCAAATAT[A/G]AGTAATTATTTCACT	1102
rs60546811	snp	A/C	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48507062	GTGGGACACTACTCT[A/C]TAGAGAAGGGCTGGG	1102
rs61447518	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529107	CCACACACGGCAAAA[C/G]TGTCATTTTCAAATA	1102
rs61948708	snp	A/C	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48504823	CTTTAGGCAGTTGCT[A/C]TCAAACCAGGAGGGA	1102
rs61948709	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48522696	AATAAAATATTCTCT[C/T]TCCTCCAAAAAGCAA	1102
rs61948710	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48525360	ACAATTCAAAAGTGA[G/T]CAAAGGATTCATGAT	1102
rs66711278	in-del	-/A			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502953	TAAGCACAGTGACCG[-/A]GGGCAGAAACAAGTT	1102
rs66947713	in-del	-/TATT	0.370772	0.218893	intron-variant	RCBTB2	GRCh38.p7	13:48527358	TATATATATGATATA[-/TATT]TATATATGATATATA	1102
rs67182812	in-del	-/GAGA			intron-variant	RCBTB2	GRCh38.p7	13:48516106	AGAGACAGAGAGAGA[-/GAGA]GAGAGAGAGAGCTGC	1102
rs67507423	in-del	-/AGAG	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48516097	AAAAGCAAGAGAGAC[-/AGAG]AGAGAGAGAGAGAGA	1102
rs67880636	in-del	-/T	0	0	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503545	CAATTTTTTTTTTTT[-/T]AAGACAGAGGAGTCT	1102
rs71076025	in-del	-/AA			intron-variant	RCBTB2	GRCh38.p7	13:48518459	TACAGAGTACTTTGC[-/AA]AAAAAAAAAAAAATA	1102
rs71076026	in-del	-/ATATAT	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48525414	TATATATATATATAT[-/ATATAT]TCAGTTATATATGTA	1102
rs71076027	in-del	-/ATGATATATATATATATGATATATATTTATAT	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48527396	GATATATATTTATAT[lengthTooLong]TAAAAGGTGCTTTGT	1102
rs71186310	in-del	-/AT	0.312348	0.242101	intron-variant	RCBTB2	GRCh38.p7	13:48527369	ATGATATATATATAT[-/AT]GATATATATTTATAT	1102
rs71960006	in-del	-/TT			intron-variant	RCBTB2	GRCh38.p7	13:48527360	TATATATGATATATA[-/TT]TATATATGATATATA	1102
rs72194233	in-del	-/AT			intron-variant	RCBTB2	GRCh38.p7	13:48527321	TATATGACTTGGCTC[-/AT]ATATATATATATATG	1102
rs72514717	in-del	-/A/T	0.000123548	0.00785868	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502951	CATAAGCACAGTGAC[-/A/T]CGGGGCAGAAACAAG	1102
rs73182514	snp	A/C	0.0091479	0.0670627	intron-variant	RCBTB2	GRCh38.p7	13:48520727	AGCAATATGAAGAAT[A/C]GAGTGTATAACCAAA	1102
rs73479220	snp	C/T	0.0748431	0.178382	intron-variant	RCBTB2	GRCh38.p7	13:48494684	CACGTGCCACCATCT[C/T]GACATCTGAGATGGC	1102
rs73479233	snp	A/T	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48509108	GACCGAGATAAGAGG[A/T]TCACTTGAGCCCAGG	1102
rs73479235	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48510883	AGAGGCAGCCTACCC[A/G]TAGGAGAGGCAAGCA	1102
rs73479239	snp	C/T	0.00246982	0.0350544	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511831	GGCTGGTTGCCACTG[C/T]TGCCGAGTCCAAGCT	1102
rs73479241	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48512631	GAATTTGAGGGAGGT[A/G]GTTATTTTAATCAAA	1102
rs73479247	snp	C/T	0.00755907	0.0610114	intron-variant	RCBTB2	GRCh38.p7	13:48515910	CCAGCTGCTTTTGGG[C/T]GGCTCACAGCCATCG	1102
rs73479252	snp	A/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48516550	CCCATGCCCTGCATA[A/T]CTCTGCATCTAAATT	1102
rs73486808	snp	C/T	0.0349115	0.127424	intron-variant	RCBTB2	GRCh38.p7	13:48520303	TGCAGAATGACCCAA[C/T]CAACTCCGTGCCCAA	1102
rs73486810	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48520701	TGATACCTGTATAAC[C/T]ATGCTTCTCCAGCAA	1102
rs73486816	snp	A/G	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48525264	AGATATTTGTAACAT[A/G]CATAATGGACAGCTT	1102
rs73486817	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48525359	CACAATTCAAAAGTG[A/G]GCAAAGGATTCATGA	1102
rs73486823	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48530279	TTACTTTAACCAACT[A/G]ATAAAACCAAACTTG	1102
rs73486824	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48531412	ATTAAGTGCTACAAA[A/G]CCGAACCAGCAGTAC	1102
rs73486825	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48532795	CGGCCTGGGCTGGGT[A/G]TAGCCCCGGAACCTA	1102
rs73486829	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533705	ATTTTGCAGTAATTT[A/G]TTATATTACACTGCA	1102
rs73486831	snp	A/G	0.0788843	0.182262	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535176	ATCAGCTACCAATGT[A/G]TTCTCTGGTCTCTTC	1102
rs74074903	snp	A/G	0.0275645	0.114116	intron-variant	RCBTB2	GRCh38.p7	13:48511092	TTTGATTATAAAAGT[A/G]AAACATGTTCAATTT	1102
rs74074904	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48514237	GAGAGTCAATCTAAT[A/G]ACTGAGACAGCTACT	1102
rs74074908	snp	C/T	0.0279526	0.114869	intron-variant	RCBTB2	GRCh38.p7	13:48515958	TGGAACCAGGTCTCC[C/T]CTACTCATTGTCCTC	1102
rs74074915	snp	G/T	0.0685596	0.171987	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533566	GTGGGGCGGAAGTCT[G/T]GTAGCCCCCTGTAGT	1102
rs74074916	snp	C/T	0.0685596	0.171987	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534577	CTGACAATTAGCTAA[C/T]AATAAAAACATGTCT	1102
rs74077637	snp	A/G	0.0279526	0.114869	intron-variant	RCBTB2	GRCh38.p7	13:48491770	GAAAGGACCCTAAAA[A/G]GTTATCACTTGGATC	1102
rs74077638	snp	A/G	0.0670745	0.170406	intron-variant	RCBTB2	GRCh38.p7	13:48493102	CCATCCGCACATCCT[A/G]TTGGCTCTACTTTCA	1102
rs74077639	snp	C/T	0.0275645	0.114116	intron-variant	RCBTB2	GRCh38.p7	13:48493152	ACCACTTTTTACCAT[C/T]CCCACAGGTGATAAC	1102
rs74077640	snp	C/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48493288	CACCCTCTCTCTCTC[C/T]CCACACACACACACA	1102
rs74077641	snp	A/C	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48493289	ACCCTCTCTCTCTCT[A/C]CACACACACACACAC	1102
rs74077645	snp	A/G	0.0256215	0.110247	intron-variant	RCBTB2	GRCh38.p7	13:48497885	GCTTCAGACACACAT[A/G]CAAGCTGCACTGCCC	1102
rs74077646	snp	A/G	0.0267878	0.112589	intron-variant	RCBTB2	GRCh38.p7	13:48498075	GTATTTCCTCCCTTA[A/G]ACCCCACCACCAATG	1102
rs74371188	snp	G/T	0.152001	0.229992	intron-variant	RCBTB2	GRCh38.p7	13:48532925	CGGGGAGGTCGGGCC[G/T]CAGGGGCGGGGAGGG	1102
rs74589555	snp	C/T	0.0275645	0.114116	intron-variant	RCBTB2	GRCh38.p7	13:48509139	AGCTACCAGCCTGGG[C/T]AATGTGGCAAAACCC	1102
rs74676300	snp	A/C	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489148	TGATCTAAAAAGTAC[A/C]AATTTATCTCATTCT	1102
rs74713432	snp	C/T	0.00835141	0.0640778	intron-variant	RCBTB2	GRCh38.p7	13:48516497	TTCTCAGCTTGTGGA[C/T]GGCTGTCTTCTCCCT	1102
rs74904583	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502407	CTAAGGCAAAAGGAT[C/T]GCTTGAACCCAGGGG	1102
rs74962194	snp	A/G	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48530052	TGTGCCACCATGCCT[A/G]GCTCATTTTTTTTTT	1102
rs75015682	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48531220	AAGGACAGGACGTGA[C/T]AGAAAATCAATTTTT	1102
rs75438861	snp	C/T	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48492646	GTGCAGACGTGCCAG[C/T]AGCATCTGGTGTGGT	1102
rs75489745	snp	A/G	0.0111196	0.0737302	intron-variant	RCBTB2	GRCh38.p7	13:48492414	GCTTCCATTTCCCAC[A/G]TCTTAAAAAAGTAAA	1102
rs75650024	snp	A/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48490697	AGGTAAGCCATAAAA[A/G]GCAGTAATGCCAAGA	1102
rs75695823	snp	C/T	0.118235	0.212457	intron-variant	RCBTB2	GRCh38.p7	13:48496668	ACTCCCAGGAGCACA[C/T]ACACATGCTGTAAGA	1102
rs75920133	snp	C/G	0.0158469	0.0875917	intron-variant	RCBTB2	GRCh38.p7	13:48493684	AGTCACCTGCTCACT[C/G]ATGTCTTGCCTCCCT	1102
rs76182128	snp	A/C			missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515322	CGTCACCTAACCCCA[A/C]ACAGCCACAGCAGTT	1102
rs76266061	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502505	CTTTCTCTCTTAAAG[A/G]AAAAAAAAAAAGTAG	1102
rs76300783	snp	A/C/T			missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512017	AATAACTTCCTTACC[A/C/T]CCCCCGTGTCTACTA	1102
rs76346016	snp	A/C	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48529391	GTTTTGTTCAGTATT[A/C]TATACATACATACAC	1102
rs76390499	snp	C/T	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48492449	TTTTACCTCAAATGC[C/T]CCAAAGCTCTTCCTT	1102
rs76558760	snp	C/T	0.0644693	0.167566	intron-variant	RCBTB2	GRCh38.p7	13:48524494	ATAGTCACCAACCAA[C/T]CAGTGTCAGAGCCAG	1102
rs76655313	snp	C/T	0.00835141	0.0640778	intron-variant	RCBTB2	GRCh38.p7	13:48524506	CAATCAGTGTCAGAG[C/T]CAGTATTTGAACCAG	1102
rs76662352	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514342	AGCAAGATGGTGAAA[A/T]ATCACCCTACTCAGA	1102
rs76717813	snp	A/G	0.030665	0.119967	intron-variant	RCBTB2	GRCh38.p7	13:48527688	CACATGACATTTCCT[A/G]TTTCAGCTGTTTTCC	1102
rs76881704	snp	G/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48528402	AAACACACTGATATT[G/T]TTAGAATTCTCTCAA	1102
rs76890985	snp	C/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48513780	TTAATGCCTGATATT[C/T]AGTAATCCGTTCTTG	1102
rs77237609	snp	C/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48498896	TTCTCTCTCAACTCA[C/G]ACCTCTCATCCCATC	1102
rs77589456	snp	A/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48516148	CTGCTCTCTAAGTCA[A/G]GAACAATGCTTGGTA	1102
rs77647251	snp	A/G	0.0441095	0.141807	intron-variant	RCBTB2	GRCh38.p7	13:48514510	TATCTCTGACTATGT[A/G]CTGCCTATTGCCACT	1102
rs77880565	snp	A/G	0.0387552	0.1337	intron-variant	RCBTB2	GRCh38.p7	13:48505781	AAAAAAGATGAGGGG[A/G]AACAGGATACAGGCA	1102
rs78008348	snp	C/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48531006	ATCCTTCAGACTCAC[C/T]GTACCCATGATGTTT	1102
rs78197458	snp	C/T	0.0670745	0.170406	intron-variant	RCBTB2	GRCh38.p7	13:48495222	TTATTATCATAACAA[C/T]ACATGGTCACTGTAA	1102
rs78440590	snp	C/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48518311	AAATCTAGTCATGTT[C/T]CCTCACGTGCCACTT	1102
rs78860799	snp	A/G	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48528575	TGAGCTGCAGACCAC[A/G]TAAATTTCAATAGGA	1102
rs79100622	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509217	CTGTAGTCCCAGCTA[C/T]TCCAGAGGCTAAGGT	1102
rs79148927	snp	C/G	0.0644693	0.167566	intron-variant	RCBTB2	GRCh38.p7	13:48493354	TCTTCTCTTCTCTCT[C/G]TCACCCTCTCTCTCT	1102
rs79553136	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534068	CTGCTACATAGGGCA[A/G]ACATTTATCTCTATT	1102
rs79682159	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48499009	CAACCCAGGAGACCA[A/T]CATCTCACACCTGAA	1102
rs79694885	snp	A/G	0.0244538	0.107838	intron-variant	RCBTB2	GRCh38.p7	13:48492204	AGCTCTCCCCACCAC[A/G]TCTCCTTGCCTATTA	1102
rs79727936	snp	G/T	0.0138799	0.0821421	intron-variant	RCBTB2	GRCh38.p7	13:48492463	CCCCAAAGCTCTTCC[G/T]TTTTATCTTTATAAT	1102
rs79776387	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520700	GTGATACCTGTATAA[A/C]TATGCTTCTCCAGCA	1102
rs79814507	snp	C/T	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48526190	TGGAAATTCAATAAA[C/T]GTTTGGTAATGAAAA	1102
rs80010455	snp	A/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48516792	TTATAAATTTGTTTG[A/T]AAGAGTTTTACCTAT	1102
rs80070363	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48521036	GTAGTAATAATATAG[C/T]AATTTCATTGCTGAT	1102
rs80167969	snp	A/C			missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515320	GACGTCACCTAACCC[A/C]AAACAGCCACAGCAG	1102
rs80311840	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48509337	CTCAAAAAATAAAAA[C/T]AAAAAAATAACAGGC	1102
rs80333011	snp	C/T	0.141258	0.225111	intron-variant	RCBTB2	GRCh38.p7	13:48531443	AAGAGTTTGGAGAGC[C/T]AGACATTTTAGGTGA	1102
rs111250183	snp	A/C/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48500506	GAGGTTGCAGTGAGC[A/C/G]GAGATCAGGCCACTG	1102
rs111267607	snp	A/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48512539	TTAAATTTTGCAATT[A/G]TGGAAGACCTTACTA	1102
rs111400966	snp	A/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48496883	TTTCATGGACACGTG[A/T]CTTCCTCCTGTTACC	1102
rs111449389	in-del	-/C	0.274574	0.248789	intron-variant	RCBTB2	GRCh38.p7	13:48532570	TCGGGACCTGTGACG[-/C]CCCCCCAGCCACACC	1102
rs111509190	snp	A/T	7.20279e-05	0.00600073	intron-variant	RCBTB2	GRCh38.p7	13:48496174	GAGGCCGGCAGCTGG[A/T]AGCAAGCTTTCCTTA	1102
rs111586084	snp	A/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48496084	TCATTTTTTAAAAAA[A/T]ATTAAATATTTCCTC	1102
rs111696012	snp	A/T	0.5	0	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534336	GCTGGCATTTTTTTT[A/T]TAAGCACCTATTGTG	1102
rs111794796	snp	C/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48492510	GCTGCCTCTATTCCC[C/T]ATCTTCAGTTCCTCT	1102
rs111796664	snp	A/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48499979	GCAGCCCCAATGGCC[A/G]TGCTAATGGGGACAG	1102
rs111842815	in-del	-/G	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48527352	GATATATATATATAT[-/G]ATATATATTTATATA	1102
rs111968475	snp	C/T	0.5	0	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502781	AGGCAAACACGTCGT[C/T]AGTGCAGGAGAAGTG	1102
rs112050421	snp	A/G	0.000598305	0.0172857	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502953	ATAAGCACAGTGACC[A/G]GGGCAGAAACAAGTT	1102
rs112173107	snp	A/C/T	0.000238765	0.0109241	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502952	CATAAGCACAGTGAC[A/C/T]GGGGCAGAAACAAGT	1102
rs112199329	snp	G/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48518423	TGAAACAGTGCTTAC[G/T]GTTTCTGCATTTACT	1102
rs112243542	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497241	TGACTTCCAAATGTT[C/T]GAGTGCCCCAGGGTT	1102
rs112374167	in-del	-/A	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48512423	AAAATGTAACACAAA[-/A]GTATCTACTTTGCCC	1102
rs112411782	snp	A/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48496085	CATTTTTTAAAAAAT[A/T]TTAAATATTTCCTCT	1102
rs112556730	snp	C/G	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48493674	TCTCTGCTTGAGTCA[C/G]CTGCTCACTGATGTC	1102
rs112567042	in-del	-/CAACA	0.140919	0.224948	intron-variant	RCBTB2	GRCh38.p7	13:48526727	CCAGCCTGGCCAACA[-/CAACA]TGGTGAAACCCCATC	1102
rs112656472	snp	C/T	0.0505692	0.150756	intron-variant	RCBTB2	GRCh38.p7	13:48492538	TCTACTTCCACGCTC[C/T]GATCAGACTTCCCGC	1102
rs112695839	snp	C/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48522165	TCTGGAACTACTGGA[C/T]GGCCTCTTACGGGAA	1102
rs112798179	in-del	-/CTCTCTCTCTCT	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48493316	ACACACACACACACA[-/CTCTCTCTCTCT]CTCTCTCTCTCTCTT	1102
rs112801132	snp	A/G	0.5	0	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512098	TGTAGGCAGCCAGTG[A/G]CTCTTCGAGGGATTG	1102
rs112897217	snp	G/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48526553	AAAAAATAAATAATT[G/T]TTTTAATGAGCTATG	1102
rs113264075	snp	A/G	0.000437904	0.0147905	intron-variant	RCBTB2	GRCh38.p7	13:48521820	ATTGATTTTCCTATC[A/G]GTGACCAATAGGTGC	1102
rs113264988	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502631	AAATAAATTATGATA[A/G]TGCACCTAACAAAAT	1102
rs113369470	snp	C/T			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534550	GGCCTTACGGTGTGC[C/T]TCAGCTGAAGCCTGA	1102
rs113468059	snp	C/T	0.00150094	0.0273535	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533046	CTCGCAGGCCGGAGC[C/T]TTGTCCGCTCCGCCT	1102
rs113469790	snp	A/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48511646	AGACTTAACCTTTAC[A/T]TTAATGAAGACATCC	1102
rs113540151	snp	A/C	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48500071	GGGTTTATTTTTATA[A/C]AATCTAAGTAATTCT	1102
rs113620619	snp	A/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48501272	TTCACAAATGTGATT[A/T]TTTAAAATCTCTGTG	1102
rs113701176	snp	C/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48522158	TAACTGTTCTGGAAC[C/T]ACTGGATGGCCTCTT	1102
rs113788449	snp	A/G	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48505671	TCTTCGTGGCCTGGT[A/G]CTGTGGGCAGGACAC	1102
rs113803113	snp	C/T	0.5	0	intron-variant	RCBTB2	GRCh38.p7	13:48496614	TGCGCCTTGAATGAC[C/T]CCTTCCCCTGCAATC	1102
rs113926349	snp	A/T	0.5	0	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499166	CTCTCTCTCTCTCTC[A/T]CTCACACACACACAC	1102
rs113977574	snp	A/G	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48516216	GAAGTTTTAGTTCAT[A/G]GGCAAGCTTTACTTG	1102
rs114037359	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48520554	CACCTCCCCTTCCTT[C/T]AAGACCTGGCATCTG	1102
rs114083040	snp	G/T	0.0310518	0.120672	intron-variant	RCBTB2	GRCh38.p7	13:48491605	CCAGATAGAGATGCA[G/T]CATCTCTTTGGCTGA	1102
rs114105848	snp	A/G	0.00701815	0.0588202	intron-variant	RCBTB2	GRCh38.p7	13:48510584	GTCCTGTTTAATCAC[A/G]ATCACCAAAGACCAG	1102
rs114272897	snp	A/G	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48507363	GCAGCAAACACCGAC[A/G]TTCCAATTTTCCAGC	1102
rs114436469	snp	A/G	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48500182	GTGACCTTACTAGGA[A/G]AGAGAGCCTTTAAAG	1102
rs114453263	snp	C/T	0.0310518	0.120672	intron-variant	RCBTB2	GRCh38.p7	13:48498086	CTTAGACCCCACCAC[C/T]AATGTGCAGACCCCC	1102
rs114454627	snp	C/T	0.0162398	0.0886349	intron-variant	RCBTB2	GRCh38.p7	13:48530685	CAATTGCAAAAACTG[C/T]GGAGACAACGTACAG	1102
rs114491347	snp	A/G	0.0162398	0.0886349	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534136	GCAAAATGGTACACA[A/G]GTATTTCTTGTAGAG	1102
rs114500570	snp	A/G	0.0162398	0.0886349	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501359	ACCATCTAAAAGTAC[A/G]CCACAAGTGATTATA	1102
rs114614401	snp	A/G	0.021333	0.101051	intron-variant	RCBTB2	GRCh38.p7	13:48492767	CAGTCTCCTTTGCTG[A/G]TGTCTCCTTATCTCC	1102
rs114658019	snp	A/G	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48509123	ATCACTTGAGCCCAG[A/G]AGCTACCAGCCTGGG	1102
rs115004436	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48514669	GAGATTTCTTGGACC[A/G]TTCAGTCTTGATGTG	1102
rs115005825	snp	C/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48513875	TATCTGCAGGAGATA[C/T]ATTCTAAGACTCTCG	1102
rs115007867	snp	C/G	0.0232847	0.105357	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502474	CTCCAGCCTGGGCAA[C/G]AGAGCAAGACCTCAT	1102
rs115147777	snp	A/G	0.0240643	0.107019	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534202	GGAAGTTGCAGCGAT[A/G]GTGCAGAGAGGCATC	1102
rs115187103	snp	A/G	0.0670745	0.170406	intron-variant	RCBTB2	GRCh38.p7	13:48495395	TTTCAAAAAATAAAA[A/G]TAGGATAAGTTTTTC	1102
rs115217624	snp	A/G	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48532429	GCCGGGCCGGTGCCC[A/G]GGACCTGGGGTACTA	1102
rs115231352	snp	A/C	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503506	ATATGCCCTACTGCT[A/C]TAAGTTCACGATTGA	1102
rs115238924	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48517248	AGTCTTTCACCACCA[C/T]GTCATCCATCCCTTG	1102
rs115276359	snp	C/T	0.0178098	0.0926698	intron-variant	RCBTB2	GRCh38.p7	13:48529270	AAAAAAATCTTAACA[C/T]GCCTGCTACAGAGAT	1102
rs115591753	snp	A/G	0.00503992	0.0499455	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502767	GGGCGTGGCAAAGCA[A/G]GCAAACACGTCGTCA	1102
rs115731845	snp	A/G	0.343579	0.231825	intron-variant	RCBTB2	GRCh38.p7	13:48496786	GAAGGGAGGGGAGAA[A/G]AGAAGAGGGGAGGGG	1102
rs115777431	snp	G/T	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48511147	TAAAAGTACTCTGAA[G/T]ATCAGAGGCATTTTT	1102
rs116061637	snp	C/T	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533640	GGATGACCTCAGTTA[C/T]CTTGGGGCCAAGGGC	1102
rs116068712	snp	A/C	0.0310518	0.120672	intron-variant	RCBTB2	GRCh38.p7	13:48500272	TTTATAAAAAGGGGA[A/C]ATTTGGACAGGGCGC	1102
rs116267343	snp	A/G	0.0236746	0.106192	intron-variant	RCBTB2	GRCh38.p7	13:48522427	AAAAAAGGAGAAATG[A/G]ATGAAAATGATGAAA	1102
rs116358336	snp	A/G	0.0322114	0.122752	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501483	ACACTTGGAGCGTGC[A/G]CTGGCTGCTCCCTGC	1102
rs116483946	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48531707	AACACGCATGTACTG[C/T]CTAGCAGGAAATAAA	1102
rs116493188	snp	C/G	0.00874735	0.0655527	intron-variant	RCBTB2	GRCh38.p7	13:48522016	GTTCGATGGAACCAG[C/G]CAGGTTAAAATTACT	1102
rs116579412	snp	G/T	0.0126979	0.078662	intron-variant	RCBTB2	GRCh38.p7	13:48491015	CCTGGAGAAGTGAGG[G/T]CAGGGTGCTGAGACC	1102
rs116580952	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48524260	TTAACAATATGTTGA[C/T]ATATATACTTAAAAT	1102
rs116653087	snp	A/T	0.0162398	0.0886349	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535075	TTAATTTTTGTATCA[A/T]TAATTTTTGGATCAT	1102
rs116654128	snp	A/G/T	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48506434	AGGCTGCAAGGGAGA[A/G/T]AAAGAATAGTCTGGA	1102
rs116973441	snp	G/T	0.0592355	0.161582	intron-variant	RCBTB2	GRCh38.p7	13:48531700	GCTTAATAACACGCA[G/T]GTACTGTCTAGCAGG	1102
rs117118911	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494187	AATGAAACATGAACT[C/G]TGCTTAGAATAATCC	1102
rs117147995	snp	A/G	0.0126979	0.078662	intron-variant	RCBTB2	GRCh38.p7	13:48532270	GCTGAGCAGAGCACT[A/G]TGTTGCGGCTTAAGA	1102
rs117248068	snp	C/T	0.00676609	0.0577691	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502546	TTACTTTTAGTTTAG[C/T]ACTGGTGTTGATTTC	1102
rs117393257	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48508776	GCAATAGATAACTCC[C/T]AATGTCCAGTTAAGC	1102
rs117406504	snp	A/G	0.0279526	0.114869	intron-variant	RCBTB2	GRCh38.p7	13:48521790	TGTGAGCCCCTCAAA[A/G]ATAGATAGTATCTCA	1102
rs117462801	snp	C/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48505584	CAAAGAGAAGTACGT[C/T]CACTGTTAGTATCGA	1102
rs117638990	snp	A/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48530936	GAACGTTTTCTCCCA[A/G]AAGAACATTTATTTC	1102
rs117731127	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514929	CAATTCATAGATCAA[G/T]AATCCAAAGTTCAGA	1102
rs117750847	snp	C/T	0.0130921	0.0798413	intron-variant	RCBTB2	GRCh38.p7	13:48525579	TTTTAAAAGAAAATG[C/T]TGATCTCAGCCCACT	1102
rs117888541	snp	A/G	0.0126979	0.078662	intron-variant	RCBTB2	GRCh38.p7	13:48531598	CTGGGATGAGGGTCC[A/G]CTTGGCGAGCCCAGC	1102
rs117919451	snp	C/G	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48499858	AGGTGCACGCTGGCA[C/G]GTCCCTGCTGTGGCT	1102
rs118114062	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48509790	ATTGTTAAGTATTCC[A/G]GCAGAAAATTAGAAA	1102
rs118137119	snp	C/T	0.00557542	0.0525036	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502656	CAAAATCCTCATTAT[C/T]AAAGTAAAGCCCTGA	1102
rs138014221	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513386	TACTACTTAAGTCAA[A/G]AAATATAACCTTATA	1102
rs138141288	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520415	AATGAGAGCATGGCA[A/G]TATGGTGTCCCTAGA	1102
rs138201857	snp	C/G	3.29788e-05	0.00406058	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511821	GCAAGGGGTTGGCTG[C/G]TTGCCACTGTTGCCG	1102
rs138261630	snp	A/C	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48526765	TACTAAAAATACAAA[A/C]ATTAGCCAGGCGTAA	1102
rs138411816	snp	C/T	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48494597	GAGCTGGAAGGTAGC[C/T]AGACAAATAATTCAC	1102
rs138460589	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496451	AGCACTGCATAGACT[A/G]ATGCTGACTGACACT	1102
rs138484907	snp	C/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48490762	TTTTTCTCTTTATGA[C/G]ACGACACAGGATGGG	1102
rs138520941	snp	C/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48531792	TCCAGCCCCCAAATA[C/T]CTGTATCAGCACATC	1102
rs138599279	snp	C/T	4.95111e-05	0.00497525	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510764	GTGTGTGCGTAGCCA[C/T]AGGCGACCTGGAAGG	1102
rs138743204	snp	A/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48514206	GGTGACTTGAACACA[A/G]GCACTATGAAACCAA	1102
rs138947822	snp	A/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499168	CTCTCTCTCTCTCTC[A/T]CACACACACACACAC	1102
rs138959406	snp	G/T	0.00795532	0.062565	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534806	TAAACTTCACTGTAT[G/T]GCTGAATTCAGTAGA	1102
rs139013532	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522037	TAAAATTACTTTACT[C/T]CTAATTAGCAGGGAA	1102
rs139113779	snp	A/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48520941	ATATCTTATAAATAT[A/T]TTCACTATGTAGTAT	1102
rs139137222	snp	G/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48527710	CTGTTTTCCTAATTG[G/T]ACGGTTCACTAATTT	1102
rs139142033	snp	A/C	0.0189856	0.0955633	intron-variant	RCBTB2	GRCh38.p7	13:48526494	TGAACCATGATCACA[A/C]CACTGCACTCAGCCC	1102
rs139171322	snp	A/G	4.94262e-05	0.00497098	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512827	TATGACAGGGCACTA[A/G]ACCATGATTAGTTGT	1102
rs139289423	snp	C/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48510209	ACTGGCAAATTTCCA[C/T]GTAGCTGAGTGACCA	1102
rs139359675	snp	A/G	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515245	ACCACTCCCATAGCT[A/G]AGGCAGGCTATTTTT	1102
rs139388448	snp	C/G	0.00795532	0.062565	intron-variant	RCBTB2	GRCh38.p7	13:48517152	TATTAACTTAGTAAG[C/G]CTCCCCTGTCCTCAT	1102
rs139502081	snp	A/G	0.0232847	0.105357	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501449	TCCAAGTATCAATAC[A/G]GTGTTCAGAGCACAG	1102
rs139627584	in-del	-/TATATTCAT	0.0729998	0.176553	intron-variant	RCBTB2	GRCh38.p7	13:48520907	TTATAACACTTCATA[-/TATATTCAT]TATATTCATTATATC	1102
rs139796076	snp	C/G	3.36129e-05	0.00409943	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515741	GAGTAGCCTGTACTG[C/G]CTGAAAAGGAAAAAA	1102
rs139812791	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48492539	CTACTTCCACGCTCC[A/G]ATCAGACTTCCCGCC	1102
rs139844871	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48523063	CTAACATTTGGAAAC[A/T]AGTAAAAAAGATATG	1102
rs140053479	snp	A/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48502066	AATCTCACAAATATC[A/T]GCTTATAAATCTGGC	1102
rs140144103	snp	A/C	0.000217557	0.0104274	intron-variant	RCBTB2	GRCh38.p7	13:48512911	CTGAAAATAAAAAGA[A/C]AGACAATCAGTTTTT	1102
rs140172279	snp	A/C	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515609	TTACTGTAGTGTATA[A/C]AACTTCATTGCCAGC	1102
rs140211811	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499724	TTCTACAATATCATC[C/T]TCGTTATCTTCCAAT	1102
rs140258547	snp	A/C	3.29457e-05	0.00405854	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510664	AGGAGTAGGATAGGA[A/C]TGGTTGCTTTTATTG	1102
rs140355761	snp	A/G	0.0119091	0.0762411	intron-variant	RCBTB2	GRCh38.p7	13:48519675	TGATCATTCTCTTCA[A/G]GGAGGTCACAATTTA	1102
rs140524314	snp	C/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48498809	TCCAGAGCAAGCCTG[C/T]TGTTCTCTATCTTCC	1102
rs140595889	snp	C/T	1.70304e-05	0.00291803	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496285	CAGAGCTTTTTCAAA[C/T]GATTTTCTCTATAAA	1102
rs140598599	in-del	-/AAAC			intron-variant	RCBTB2	GRCh38.p7	13:48498437	TGGGCCGATAAAAAA[-/AAAC]CTGCCACTCGCGGCC	1102
rs140643232	snp	A/G	0.00901601	0.0665361	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502779	GCAGGCAAACACGTC[A/G]TCAGTGCAGGAGAAG	1102
rs140735851	snp	A/C	0.0115144	0.0749975	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535186	AATGTGTTCTCTGGT[A/C]TCTTCCAAAATGTCT	1102
rs140807796	snp	C/T	8.25294e-05	0.00642323	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502854	CCACATGTACACGTG[C/T]CCACCCTGCGTCTTG	1102
rs140909247	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48516303	GACAGGAATTAACAC[C/T]CAGAAAACACGTGTA	1102
rs140924847	snp	A/G	1.648e-05	0.0028705	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490208	GTTTGTGTTACTACA[A/G]TCAGATGGTTTATGC	1102
rs141031461	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519128	CAGTGGATGAGCCAG[A/T]TTAAAGCCCAGAGTT	1102
rs141051136	snp	A/G	0.000834988	0.0204156	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502728	GACCAGCTTACCCAC[A/G]GAGAGGAGGCGCCAC	1102
rs141051527	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48530862	TATAAAAAATGGTGA[C/T]GTTTATCACAAGGGT	1102
rs141149048	snp	A/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48513759	TATAATTGGTGTCTG[A/T]TAATTTTAATGCCTG	1102
rs141150281	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503084	TCATACACCTCATCT[C/G]CTAAATTATCAGGCA	1102
rs141360429	snp	A/T			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499164	CTCTCTCTCTCTCTC[A/T]CTCTCACACACACAC	1102
rs141373575	snp	A/G	8.43433e-05	0.00649342	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502749	GAGGCGCCACGTGAC[A/G]GCGGGCGTGGCAAAG	1102
rs141381338	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48504506	TAAGGCCCAGTTCAA[A/G]CTGCCCCAAGTTTGA	1102
rs141393239	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489236	TTATACTGGTGCCAG[A/G]TTAAGAGACCTATTT	1102
rs141483632	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48509990	AATGAAAAGTGGAAA[A/G]GCAGTGATCTGACCA	1102
rs141636087	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48496012	GCTTCTGCCTTTGAT[A/G]TCCATCCCAACATTA	1102
rs141670973	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531987	TAAACAGTGTCTGGG[G/T]GAAAGAGCAACGATC	1102
rs141679808	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530438	CACACTTTACTTTCT[A/G]AAATTATTCCTCTCC	1102
rs141891385	snp	C/T	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48516200	ACCAAGGAAATGGTC[C/T]GAAGTTTTAGTTCAT	1102
rs142002915	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521836	GTGACCAATAGGTGC[C/T]TCATGAAGTATGTTT	1102
rs142047127	snp	C/G	3.3024e-05	0.00406336	intron-variant	RCBTB2	GRCh38.p7	13:48511880	CCCAGACATAGACCT[C/G]AGAGAAAATGAGACC	1102
rs142110650	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508202	CCGGGGTTCCCCAGG[A/G]ATAAGTTATGACATA	1102
rs142120538	snp	C/T	9.90802e-05	0.00703778	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521941	AGTTCTTCTTCCATA[C/T]GGACTCAGTCCTGGG	1102
rs142244617	snp	C/T	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48531468	AGGTGAGGTAGTCAC[C/T]TCTCTGAAATGATGG	1102
rs142277401	snp	A/C/G	0.00993419	0.0697739	intron-variant	RCBTB2	GRCh38.p7	13:48498126	AGGGTAACCTGGGTT[A/C/G]GGGGTGGATAGAGCT	1102
rs142354661	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48524721	CTGTTCCTTTTAGAT[C/T]CTTGTAAAGTTGTCT	1102
rs142360397	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48526999	TTTATACTATTGTAC[C/G]TGTAAGAAAAATCCA	1102
rs142443945	in-del	-/AC			intron-variant	RCBTB2	GRCh38.p7	13:48499112	CCGACCCCCACCCCA[-/AC]ACACACACACACACA	1102
rs142598206	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48507814	AGTTTAAAATATGCC[A/G]TTAGGGAACGTTAAG	1102
rs142622773	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532235	AAAGTTTTCAATGTC[C/T]GAAAACCTCTATTTC	1102
rs142750034	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496597	CCTAGGAAAAAAGCA[C/T]GTGCGCCTTGAATGA	1102
rs142769472	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48500297	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	1102
rs142770201	snp	C/T	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48505200	TTGGTTTCATCACAT[C/T]GCAAGGGTGGTGTGA	1102
rs142909477	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48506834	ACTAGGCAAAGACTT[C/T]TACATTTTTTGGAAT	1102
rs143013589	snp	A/G	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48491153	AAATAAAAGCCCCAA[A/G]TACTTTCTAAGCAAT	1102
rs143051786	snp	A/C	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48500175	TCAAAATGTGACCTT[A/C]CTAGGAAAGAGAGCC	1102
rs143079901	in-del	-/T	0.0232847	0.105357	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503471	AGCCCAGGAGAGCAG[-/T]TTCCTAGGATCACTA	1102
rs143122031	snp	A/G	0.000236574	0.0108734	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502744	GAGAGGAGGCGCCAC[A/G]TGACGGCGGGCGTGG	1102
rs143158335	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48504149	CCACTGGGGGGTCAG[A/G]TACACCCCACATCTG	1102
rs143282542	snp	A/C	0.00676609	0.0577691	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489940	CAATGCTTTCTACAT[A/C]AACTCTGGGTTTAGG	1102
rs143342113	in-del	-/AAAAAAAAAAAAAAC			intron-variant	RCBTB2	GRCh38.p7	13:48516884	AATAAGATACATAAA[-/AAAAAAAAAAAAAAC]CAGCCAATATGTCTA	1102
rs143366916	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534317	GCTCACTTCAGTGAT[A/G]ATAGCTGGCATTTTT	1102
rs143474947	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503740	TTTTTGTAGAGACAA[G/T]GTTTTGCCATGTTGC	1102
rs143528188	snp	A/G	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48509145	CAGCCTGGGCAATGT[A/G]GCAAAACCCTGGCCC	1102
rs143552627	in-del	-/TT	0.0685596	0.171987	intron-variant	RCBTB2	GRCh38.p7	13:48529801	AACTCTCTTTTAGTC[-/TT]TAACAAGAGTCCTTA	1102
rs143596230	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48523915	GTTAAGACATAATTG[C/T]ATGTATGTCATGGAA	1102
rs143605613	snp	A/G	0.000153988	0.00877328	missense, synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511781	GTACCCTCTGGACAC[A/G]GATGCCTTGCAAAGC	1102
rs143697932	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530615	ACAGAAAAGCAATGA[A/C]CATTCTTAGAAAAGA	1102
rs143833499	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48528362	AATTCAACTTAATGA[A/G]ATCAACTCTAAAGCT	1102
rs143963317	snp	A/C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48491898	AATTGGCATAGGGTG[A/C/G]TGGTACTGGTTATAG	1102
rs143973519	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48522359	ATCACGGGGAAGAGC[A/G]GACATCAATTCTCAG	1102
rs143982828	snp	G/T	0.000247066	0.0111118	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510665	GGAGTAGGATAGGAC[G/T]GGTTGCTTTTATTGC	1102
rs144002225	snp	A/T	8.24627e-05	0.00642063	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515640	ACTGCCAAAGACACA[A/T]GCCTGACGAATTAAC	1102
rs144174727	in-del	-/GTTT			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533893	CTTTTATACTGGCTG[-/GTTT]TTTCATGAGGACACT	1102
rs144186814	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501528	CGCCACTTTTCAAGC[C/T]TAAGGAACGCCTATG	1102
rs144402548	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526874	TGATCCAAGATCACA[C/T]CACTGCACTCCAGCC	1102
rs144508754	snp	A/T	0.0107246	0.0724382	intron-variant	RCBTB2	GRCh38.p7	13:48532101	AATGCGTTTTGTTAT[A/T]GTCCTGGTCTCGAAC	1102
rs144657295	snp	G/T	1.64906e-05	0.00287142	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515648	AGACACAAGCCTGAC[G/T]AATTAACTGTAGTTC	1102
rs144702097	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48501169	GTTCTCTGTCTGGAT[A/G]TGGGGCAGTGGTTTC	1102
rs144740669	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519254	CTATTCTCAGACTCC[C/T]TAAGGAACAGGCAAT	1102
rs144786903	in-del	-/GTTTTAGTTTTTTTT			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489590	AATAATTACAGGCTG[-/GTTTTAGTTTTTTTT]TTTTAAGTTTATTTT	1102
rs144797596	snp	C/T	8.2826e-05	0.00643476	synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502878	CGTCTTGGCCGCAGA[C/T]GTGTGTGTGGAGTGA	1102
rs144858453	snp	A/C/G	0.000297858	0.0122001	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502873	CCCTGCGTCTTGGCC[A/C/G]CAGACGTGTGTGTGG	1102
rs144859518	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48514079	TAACAACCTCAGCAT[C/G]GAAACTCTCCATTTT	1102
rs144919275	snp	C/T	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48511356	CTAATCATTAACTTA[C/T]GATTTGATTAGTAAA	1102
rs144955234	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48516338	TTTGTTAAGGCAGCC[A/G]TAACAAAGTAGTGAC	1102
rs145099808	in-del	-/T	0.0189856	0.0955633	intron-variant	RCBTB2	GRCh38.p7	13:48511386	TACACCTATTTTTTT[-/T]ATTAAAGTTATCCTC	1102
rs145149802	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48495199	AAGATTGGTTTTCTT[C/T]CCTTTCTTTATTATC	1102
rs145290900	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48492828	TAATCTTCAAACCTG[C/T]CTCACGTCACTGCCT	1102
rs145312321	snp	A/G	0.162909	0.23434	intron-variant	RCBTB2	GRCh38.p7	13:48496840	GGAGGGGAGAGGAGG[A/G]GAGGGGAGAGGAGGG	1102
rs145348673	snp	A/G	0.000165769	0.00910258	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501838	AATTCCCTCTTCAGT[A/G]ACTCAGCCACTGTGA	1102
rs145457559	snp	A/G	0.00557542	0.0525036	intron-variant, missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517312	TTGGTTAATGAACAA[A/G]TAAATGAATGGCTGT	1102
rs145466956	snp	A/G	6.58946e-05	0.0057396	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490114	CTGCAGATGGGATCA[A/G]TTTTTAAAGGCTCCA	1102
rs145469458	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499704	GGATATGAAAATTCA[C/T]TCATTTCTACAATAT	1102
rs145474851	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502982	TTGGGTCCTCCTCCC[A/G]CCAGGTTTAACTGAT	1102
rs145769891	snp	A/T	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48494178	TGAGGAGTAAATGAA[A/T]CATGAACTGTGCTTA	1102
rs145801442	snp	C/T	0.0023933	0.0345097	intron-variant	RCBTB2	GRCh38.p7	13:48494482	GGTATTTAGTAGGTA[C/T]CTACTCTGTGTCAGA	1102
rs145831644	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48506649	TGTACACATAGCTGA[A/G]CAATTAATAAAAGGA	1102
rs145924662	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527162	CAGAAGCTGGCAACA[A/G]TATTGGGAAGATTTT	1102
rs145951611	snp	A/G	0.02016	0.0983543	intron-variant	RCBTB2	GRCh38.p7	13:48531503	TGTTTCAAGACTTAA[A/G]TAAAGTTCTGTGCCA	1102
rs146045257	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505684	GTGCTGTGGGCAGGA[C/T]ACGCGGATCAGAGTC	1102
rs146073971	snp	G/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48509694	ACTTTTAAAACATAG[G/T]TTAAAGAAAGTCAGC	1102
rs146308003	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48526163	ATTCTAATTTTGCCT[C/T]TACCAAGGACATGGA	1102
rs146338388	snp	A/G	0.000807162	0.0200731	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512118	TCGAGGGATTGGCTG[A/G]TTAACTGTTGATCCA	1102
rs146429069	snp	C/T	4.94711e-05	0.00497324	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515647	AAGACACAAGCCTGA[C/T]GAATTAACTGTAGTT	1102
rs146456746	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48529225	TCCATTTTAAATCTC[A/G]GTCCTTATAGATTTA	1102
rs146458203	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48522655	TCATTATGTAGTTAA[C/T]GATTTCATCATTAAA	1102
rs146463569	snp	A/C/T	0.000461228	0.0151792	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510733	ATACACTTGGCCTTC[A/C/T]TCTGTTAATACTAAT	1102
rs146494175	snp	C/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48518972	TAATGTAGATGTTAA[C/T]AATCTAATAATGTCT	1102
rs146922249	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503518	GCTCTAAGTTCACGA[C/T]TGATGAGGAGGTAAT	1102
rs146931834	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48507819	AAAATATGCCGTTAG[A/G]GAACGTTAAGAACAA	1102
rs147261845	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490138	GGCTCCAACTCTGCT[C/T]GCTTTGCTGATAAAG	1102
rs147286833	snp	C/T	0.00153143	0.0276292	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510748	ATCTGTTAATACTAA[C/T]GTGTGTGCGTAGCCA	1102
rs147415321	snp	C/T	0.00716266	0.059414	intron-variant	RCBTB2	GRCh38.p7	13:48496601	GGAAAAAAGCATGTG[C/T]GCCTTGAATGACCCC	1102
rs147496668	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48521494	AGATGTGATGAAGAA[A/G]GAAATTAAAGAATGT	1102
rs147513042	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48493066	ACCTCCTCAGTCGTC[-/T]TTTTTTTCCTCACAT	1102
rs147542480	snp	C/T	0.00517822	0.0506191	intron-variant	RCBTB2	GRCh38.p7	13:48516837	GCATTTTTATTGATA[C/T]ACTTTTCAACTTGCC	1102
rs147562316	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507991	CATCATAAATAAAAT[A/C]TTTTTCTGGGAAAGA	1102
rs147572201	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48511393	TACACCTATTTTTTT[A/T]ATTAAAGTTATCCTC	1102
rs147666176	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489750	AGACAGCACTCCTTG[C/T]CAAGCTATCTATGTG	1102
rs147873740	snp	A/C	0.0178098	0.0926698	intron-variant	RCBTB2	GRCh38.p7	13:48530333	AAGCAAATTCCATGG[A/C]CTCCTTACATTTATG	1102
rs147883543	snp	C/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48532808	GTGTAGCCCCGGAAC[C/T]TAGCTCTTAACTCCC	1102
rs148106047	snp	C/G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530694	AAACTGTGGAGACAA[C/G/T]GTACAGTTTTTCTCA	1102
rs148190874	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48500287	AATTTGGACAGGGCG[C/T]GGTGGCTCACGCCTG	1102
rs148219295	in-del	-/A	0.039522	0.134904	intron-variant	RCBTB2	GRCh38.p7	13:48505762	ACCATCTTTTCAAAG[-/A]AAAAAAAAAGATGAG	1102
rs148244769	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48504420	AGGCTTTCTCATTGA[C/T]CTTCAATGACTTCAT	1102
rs148275628	snp	A/G	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48519536	ACTCTACTGGCTACT[A/G]GGATTCCAATGCGTG	1102
rs148279651	snp	C/T	0.00103073	0.0226782	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502748	GGAGGCGCCACGTGA[C/T]GGCGGGCGTGGCAAA	1102
rs148368922	snp	C/T	0.0232847	0.105357	intron-variant	RCBTB2	GRCh38.p7	13:48495337	CAGTCTTTTTTTCTA[C/T]GTAGATAATGAATTT	1102
rs148420633	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48532216	GCCAAGACGGAGCAC[C/T]TGGAAAGTTTTCAAT	1102
rs148551009	snp	A/G	0.000230665	0.0107368	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510631	ATGCCCGTGTTACCT[A/G]TCCTTTTCCACAGTG	1102
rs148554011	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506747	GGTTAGGGCAGCCCA[A/G]TGAACAATGTGAAGA	1102
rs148597426	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521553	AGATCAGACAGTTTA[A/T]AATTTTAAAAATCTC	1102
rs148628911	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491941	CATAGAAAACAAGGC[C/T]CCCATTATTTTTCAG	1102
rs148681694	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497933	CCAAGCCCCAGCTCT[A/G]CGCCTCCTCCACGCA	1102
rs148787709	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526976	AATAACATATCCAAT[C/G]AGTAGCATTTATACT	1102
rs148860305	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517728	AATGCTGTAGCTAAA[A/T]AGAGCTCAAAAGATA	1102
rs148945272	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48494392	TATTATACTAATTTA[C/G]GGTACAGCAATTAGC	1102
rs148994928	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499420	GCTCCACGGTGGTGA[C/T]GATTTGATTCTTCTC	1102
rs149152195	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534051	AATGTATAACTGCCT[G/T]TCTGCTACATAGGGC	1102
rs149175309	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489791	GCTGAATAATGGAAC[A/G]TTTGGGCCAGAATAG	1102
rs149323909	snp	A/T	0.00835141	0.0640778	intron-variant	RCBTB2	GRCh38.p7	13:48501027	AAAGAAGCCAAGCAC[A/T]AATGAATGCATCCTG	1102
rs149490973	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48491774	GGACCCTAAAAAGTT[A/G]TCACTTGGATCCATG	1102
rs149613565	snp	A/C	8.24192e-05	0.00641894	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515246	CCACTCCCATAGCTG[A/C]GGCAGGCTATTTTTT	1102
rs149647589	snp	A/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48526786	CCAGGCGTAAGAGTG[A/T]GTACCTGTAGTCCCA	1102
rs149664060	in-del	-/A	0.0287284	0.116357	intron-variant	RCBTB2	GRCh38.p7	13:48525092	TCCATGTGGAAATGT[-/A]AAAAAAAAGCAAAAC	1102
rs149667011	snp	C/T	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48517155	TAACTTAGTAAGCCT[C/T]CCCTGTCCTCATTAC	1102
rs149679609	snp	A/G			synonymous-codon, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501756	CCGAATCTTGAGAAG[A/G]ACTTTATGTGCATAA	1102
rs149711659	snp	A/G	0.00597247	0.0543191	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488617	ACCACTCTGGTGGGG[A/G]GTGTTGACAGCAGGG	1102
rs149764637	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493696	ACTGATGTCTTGCCT[C/T]CCTGACCATTCTATT	1102
rs149924456	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527866	ATAATGTGATAAACA[C/T]ATTCATTCTTAATCC	1102
rs149974463	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533635	CAGGGGGATGACCTC[A/G]GTTACCTTGGGGCCA	1102
rs150038571	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48510273	GCCAGGGAAGAGCGA[A/C]CTTGAATGTTATTGA	1102
rs150054311	snp	A/G	0.000131785	0.00811635	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499660	TGATGCTGTCTGTGT[A/G]TAGGTATTCCAGGAA	1102
rs150104825	in-del	-/CT			intron-variant	RCBTB2	GRCh38.p7	13:48493277	CTTCTCTCTCTCACC[-/CT]CTCTCTCTCTCCACA	1102
rs150107579	snp	A/C/T	0.00189423	0.030719	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510756	ATACTAATGTGTGTG[A/C/T]GTAGCCACAGGCGAC	1102
rs150361530	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512948	ATCTACTTCATTATA[C/T]GAAAATATATGTAGC	1102
rs150415091	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48519714	CAAATAATTACAATA[C/T]AACCTAAGTACAACA	1102
rs150466265	snp	C/T	0.00953873	0.0683987	intron-variant	RCBTB2	GRCh38.p7	13:48526589	ACCACTGCACATTAG[C/T]CTAAGCAACAGAGCA	1102
rs150478484	snp	A/G	0.0039699	0.0443756	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502797	AGTGCAGGAGAAGTG[A/G]GTGAGGTGCGGGAGG	1102
rs150498063	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48496445	CAGTGAAGCACTGCA[G/T]AGACTGATGCTGACT	1102
rs150551644	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48500821	GTACTGTGTTACAGC[A/G]AACAAATCCACCCCC	1102
rs150560967	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532259	CTATTTCCAGGGCTG[A/C]GCAGAGCACTATGTT	1102
rs150792784	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48504730	TGAGGAAGACTCAAC[A/G]ACACAGAGCAAAGGT	1102
rs150840418	snp	C/G/T	0.000131869	0.00811909	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515240	TGTGGACCACTCCCA[C/G/T]AGCTGAGGCAGGCTA	1102
rs151044853	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48523920	GACATAATTGTATGT[A/G]TGTCATGGAAATTAC	1102
rs151103661	snp	A/G	0.000131776	0.00811608	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510662	ACAGGAGTAGGATAG[A/G]ACTGGTTGCTTTTAT	1102
rs151171441	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512481	TTTTCTTATTGCAAA[C/T]AACCTCTTTACTACA	1102
rs151236604	snp	C/G	0.00676609	0.0577691	intron-variant	RCBTB2	GRCh38.p7	13:48498718	CTGGGCAACAAGAGT[C/G]AAACTCTGTCTCAAA	1102
rs151299421	snp	C/T	0.00787698	0.0622611	missense, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502727	TGACCAGCTTACCCA[C/T]GGAGAGGAGGCGCCA	1102
rs151336600	snp	A/G	3.37975e-05	0.00411067	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496272	GATAGTTTGTTGGCA[A/G]AGCTTTTTCAAACGA	1102
rs180677663	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48524708	GTCATCTTTAATCCT[A/G]TTCCTTTTAGATCCT	1102
rs180691951	snp	G/T	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48532954	GGGTGGCCTGCCCCA[G/T]TGGTACCTGACAGCA	1102
rs180760819	snp	G/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502504	TCTTTCTCTCTTAAA[G/T]AAAAAAAAAAAAGTA	1102
rs180894409	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48507197	TCAGGGGTGGGGCGC[A/G]GATTTGGTTGGCTGC	1102
rs180963624	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527601	CCAAATGGGACACTC[A/G]GTGGCCAGTAGTTCA	1102
rs180996591	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48519518	TATGGTACCCAGCCC[A/G]TAACTCTACTGGCTA	1102
rs181007368	snp	A/G	0.0046737	0.0481145	intron-variant	RCBTB2	GRCh38.p7	13:48496327	TCTAGCAGTCCTGGC[A/G]GAAAGAGGTGTTTAT	1102
rs181175856	snp	C/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502347	AGTTTCTTTAAATTA[C/G]CCAGGCATGGTAATG	1102
rs181203396	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491711	CAGTTTGATGCCTCA[C/G]AGATCTGGACAGCAT	1102
rs181230943	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513995	CAATAACTAATAATC[A/C]AAGAGAACAATTACA	1102
rs181245484	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534813	CACTGTATTGCTGAA[C/T]TCAGTAGACTAAAAA	1102
rs181271164	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48523895	TTCTGTTTATCTGAC[A/G]TCAGGTTAAGACATA	1102
rs181447042	snp	C/T	0.00636936	0.0560724	intron-variant	RCBTB2	GRCh38.p7	13:48508862	TTTCTCCCACCTTGA[C/T]GCCCCACAATCCATC	1102
rs181447182	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529516	CATAGGGAGATATAC[A/G]TAAGAGATATTAGCT	1102
rs181488250	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517959	CGAGAGGGCACACAG[C/T]GATGCACAGGGAAGA	1102
rs181580674	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513173	GGCTGCTGGGAGTAA[C/T]AGCAAAAACATTAGA	1102
rs181656247	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534180	AAAAAGTAAGTATAC[A/G]TTAACAGGAAGTTGC	1102
rs181667419	snp	C/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48495601	CTTGTGAGTGAATTC[C/T]TTGAAGAATTATGTC	1102
rs181812651	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48507823	TATGCCGTTAGGGAA[C/T]GTTAAGAACAAAGAT	1102
rs182012790	snp	A/C	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48490901	GTGTTTTCTGGCTTA[A/C]TGTAATGCACTCTGG	1102
rs182079819	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48528815	TACCTACATGGCTAA[A/T]TAAAATGGAACAATT	1102
rs182098644	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48514136	TCTCTTTGGCATATC[C/T]AAATTGCAAGCATCA	1102
rs182161161	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534961	GAGCTGTGCATGCTC[C/T]TATTTAAGTTCAACT	1102
rs182176115	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492391	GAGTCATTTGCATCA[C/T]TAGACAAGCTTCCAT	1102
rs182281411	snp	A/G	0.000557155	0.0166813	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48522349	AAAGTTCCAAATCAC[A/G]GGGAAGAGCGGACAT	1102
rs182354692	snp	A/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48500707	GAGGCAGGAACAGAT[A/T]CTCACTCACAGCCTC	1102
rs182439876	snp	C/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48526439	TACTTGGGAGGCTAA[C/G]ATAGGTGGATCGCTT	1102
rs182480139	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48504801	GAGGATGATCCTCCA[C/T]TGCCTCCTTTAGGCA	1102
rs182570432	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48526073	GATTTTAAGCTTAAA[G/T]TAATCATCTCAGGAT	1102
rs182632368	snp	A/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48505121	AATCCTCGCTCTACC[A/T]CTAGGCTGCGTGACT	1102
rs182741548	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509034	TGTAGGAGCACCATA[A/T]AAAGTAATGGGCCAG	1102
rs182964462	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48530431	GGGGAAACACACTTT[A/G]CTTTCTAAAATTATT	1102
rs183028282	snp	C/T	0.0387552	0.1337	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503468	TGGAGCCCAGGAGAG[C/T]AGTTTCCTAGGATCA	1102
rs183122214	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535154	GTTCCTTGATTATAT[A/G]TCCCCTATCAGCTAC	1102
rs183402380	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530771	AGTGTCTTCATTTGA[C/T]GTGCTAAGTTAAACT	1102
rs183472301	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498289	TCTTAATGAAATTAC[A/G]TTTTTCAAGGTGGGA	1102
rs183487866	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494383	CTTATAGTCTATTAT[A/G]CTAATTTAGGGTACA	1102
rs183493904	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48515865	CATCCATTTTTGAGA[A/G]GCCTCTCGCAGCTGC	1102
rs183626608	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514855	AGTCACTCTTTAGTG[A/T]AAGAATCACAGAATG	1102
rs183795175	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48525646	AACACTGCCCTAGAT[A/G]AACTCTAGAGCATAC	1102
rs183800930	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48497480	CATCTGAAAGATCCT[A/G]TTTGTTTTTCTGAAT	1102
rs183839974	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492685	CTTCCTTCCTGTTTC[C/G]CTTTCTTTCCCAGCC	1102
rs184014853	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48520867	AAAAAATGCCAACAC[C/T]TCAACTTTTGAGTAC	1102
rs184185332	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527547	TAAGTAACCTCTCCA[C/T]GCAGAAGTTCCTGCC	1102
rs184250517	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48527677	AGGTAATCTGTCACA[C/T]GACATTTCCTATTTC	1102
rs184254038	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506748	GTTAGGGCAGCCCAA[C/T]GAACAATGTGAAGAT	1102
rs184376882	snp	A/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48510913	ATTAAGTTAACCAAC[A/T]TCCTTCCAGAACATG	1102
rs184387476	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502241	CACCTGTGATCCCAA[C/T]ACTTTGGCAGGGGCA	1102
rs184433378	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48507262	TAGAGGGTACTTTCA[A/G]GTCTAGGCTTGTGAC	1102
rs184466397	snp	A/C	0.00438332	0.0466095	intron-variant	RCBTB2	GRCh38.p7	13:48511307	CTTTGTATACAATAC[A/C]TCATCTCCAGCATAT	1102
rs184476224	snp	C/T	0.00318978	0.0398085	intron-variant	RCBTB2	GRCh38.p7	13:48523109	ATTACTTAGAAGTTT[C/T]TCACTTAAAAATTTA	1102
rs184632603	snp	A/G	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48505880	AAGGCTTCCTTCCGT[A/G]ACTAAAAGTGTTTAC	1102
rs184660202	snp	C/T	0.0329836	0.124112	intron-variant	RCBTB2	GRCh38.p7	13:48532794	GCGGCCTGGGCTGGG[C/T]GTAGCCCCGGAACCT	1102
rs184714579	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526647	AGCCTGGGCGCGGTG[G/T]CTCATGCCTGTAATC	1102
rs184777282	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490821	CCTTCAATAATCTCA[A/G]CTGGGAAAATGCTTT	1102
rs184784769	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48512556	GGAAGACCTTACTAC[A/G]TACAGGTAAATGTCA	1102
rs184787187	snp	G/T	0.00835141	0.0640778	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533289	CGCCCCCTCCCCTCG[G/T]AGTTGACCCCCGGGA	1102
rs184834507	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48493891	TGTTTTGTTCATTTG[C/T]AGTACCCCAGTGCGT	1102
rs184999606	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489220	AGCTAGTGCTTTATA[G/T]TTATACTGGTGCCAG	1102
rs185291130	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48496855	AGAGGGGAGAGGAGG[A/G]GAGGGGAGACCCTTT	1102
rs185403592	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48494967	TTATATGAAAGTGCT[A/G]ATGTTCTCTGGTTGA	1102
rs185441493	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502469	CCGCACTCCAGCCTG[A/G]GCAACAGAGCAAGAC	1102
rs185458200	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491721	CCTCACAGATCTGGA[C/T]AGCATCAGGAAAATT	1102
rs185472569	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48524161	CATAATAAAGAAAAC[C/T]ATCATCCCCAATTTG	1102
rs185622409	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48500956	GACTCACTGCAGTAG[A/G]ATTTAAATATCTGTT	1102
rs185708193	snp	A/C	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48522756	TTTTTCTAATTGACG[A/C]GGTAGGGTCTATTTA	1102
rs185769818	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48525804	AAAACAATGTTCACC[A/G]AAATCACTAAGTCAC	1102
rs185796169	snp	C/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48495849	AACTGTTCCTATTGT[C/G]TTTTTGTTTTTCACT	1102
rs185857591	snp	C/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48504339	TAACTCCATCCATGA[C/T]TTGGCGTCACCTCTG	1102
rs186004270	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48508700	TGAGTGCCTGGCCCA[C/T]CCATGATTTTTATAA	1102
rs186109565	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48528888	AAACTAGCACACAAC[C/T]TCAAAGGAAATGGTA	1102
rs186206603	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514064	TCTTACCATAAATCT[C/T]AACAACCTCAGCATG	1102
rs186339767	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534894	TCACCACATCTCCCA[A/C]GTTTACCTACATCTG	1102
rs186369574	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508907	CCTGAATCAGAAGCC[C/T]TGGGTGATCATTCTG	1102
rs186480107	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534974	TCTTATTTAAGTTCA[A/C/G]CTCTTCCACCTTTGT	1102
rs186582750	snp	A/C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48500835	CAAACAAATCCACCC[A/C/T]CCTTCTTTCATGCAG	1102
rs186632005	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48522426	AAAAAAAGGAGAAAT[A/G]AATGAAAATGATGAA	1102
rs186657143	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48518330	CACGTGCCACTTGGA[A/T]CATAAGACCTTGCCC	1102
rs186671151	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534491	GATCTGTTTGCCTTG[C/T]GCACTTGGTCTTTTA	1102
rs186715630	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48491473	CATCACAGCATACTA[C/T]ACATAAAAATGTGCT	1102
rs186845088	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48526314	GCACTTTGAGGATCG[A/C]TTGAGGCCCCCAAAA	1102
rs186900066	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48493977	TAAATACTCCTGATT[G/T]CAAAATACTGAGGAC	1102
rs186907617	snp	C/T	0.000164864	0.00907771	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515285	AAAGAATCCAGTCTC[C/T]GAGGTTCAATGGTGC	1102
rs186940891	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513182	GAGTAATAGCAAAAA[C/T]ATTAGAATGAAGTCA	1102
rs187009773	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48521066	TTCTGTGAAACTATT[A/C]TTTATTTTATGAAAG	1102
rs187045637	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48498456	CCACTCGCGGCCGGG[C/T]GCAGTGGCTCACGCC	1102
rs187066325	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48522290	ACTTCCTGTGATAAG[C/G]AAAAATAAATTTTAG	1102
rs187189719	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502972	CAGAAACAAGTTGGG[A/T]CCTCCTCCCGCCAGG	1102
rs187239131	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497654	AAGGTACTTAATAGA[A/G]TGTACGAAGTATAAA	1102
rs187457974	snp	C/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48506278	TGCCAGGAACAGTGG[C/T]GTCGGCTTCAATCCA	1102
rs187488750	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48526964	ATAGGAGGATTAAAT[A/G]ACATATCCAATGAGT	1102
rs187506260	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48524934	TATTATAAAAATACT[A/G]AAGTTATAAAATGTA	1102
rs187588116	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48530647	CTTCACTAGTCATCC[A/G]CAGTCAGAGGGACAT	1102
rs187588171	snp	A/T	0.00358779	0.0422022	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488488	TGGACACAGGTCATT[A/T]TACATTTGTCCAAAC	1102
rs187698666	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48530795	TTAAACTGTAAACTC[C/T]TGAATAATTTGAACT	1102
rs187770018	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489134	TAGGTAATTTGTTTT[A/G]ATCTAAAAAGTACAA	1102
rs187770525	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48509042	CACCATAAAAAGTAA[C/T]GGGCCAGGCCAGGCG	1102
rs187778612	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48510338	AGGGCAAAAGGGTGA[C/T]TTGTAAGGCAGAAGA	1102
rs187927997	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514486	ACGGGAGACTACTGT[A/G]TATCTGGTTATCTCT	1102
rs188087751	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48490398	GTAATACCTAAAGAA[C/T]AGTCATAAAAAGTAT	1102
rs188133990	snp	A/C	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48505046	GTTTGTTTTTTATTT[A/C]TTTCTTTTTTTTTTT	1102
rs188140423	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48510971	TGAGTACCCTGGCGT[A/G]AGCACCTGCCCCAGT	1102
rs188281637	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48492729	CTGCTGGTTTCTCTC[C/T]TCCGTTACTGCTCAC	1102
rs188319200	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48524180	ATCCCCAATTTGCAT[A/G]TATAGTTTGTGCACT	1102
rs188394597	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48531457	CCAGACATTTTAGGT[A/G]AGGTAGTCACCTCTC	1102
rs188414907	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489224	AGTGCTTTATAGTTA[C/T]ACTGGTGCCAGGTTA	1102
rs188546049	snp	A/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48519398	ATAAAATCAAGTGGT[A/T]TTCTGGATGTCTAGA	1102
rs188574104	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48514973	GTCCACAATCAGTTC[A/G]TCAGTGTTTACTGGG	1102
rs188825828	snp	A/C	0.00358779	0.0422022	intron-variant	RCBTB2	GRCh38.p7	13:48505149	ACTAGCACTAGGCTG[A/C]GTGACTAGGGGAATG	1102
rs188848952	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48502261	TGGCAGGGGCAGAGA[C/T]AGAAAGATGGTCTGA	1102
rs189122870	snp	A/C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48532869	CTAGGCCTGTGGCAC[A/C/G]GTCGCGGCTCTAGTC	1102
rs189143509	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48490837	CTGGGAAAATGCTTT[A/G]AAGAAATCATGACTT	1102
rs189153804	snp	C/T	0.000115717	0.00760559	intron-variant	RCBTB2	GRCh38.p7	13:48512715	TCAATGAGCTTTATG[C/T]TGACTGTTCTCACCT	1102
rs189198733	snp	A/C	0.00319074	0.0398324	intron-variant	RCBTB2	GRCh38.p7	13:48526593	CTGCACATTAGCCTA[A/C]GCAACAGAGCAAGAC	1102
rs189202501	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533645	ACCTCAGTTACCTTG[A/G]GGCCAAGGGCTTCGA	1102
rs189229935	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502470	CGCACTCCAGCCTGG[G/T]CAACAGAGCAAGACC	1102
rs189452977	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48527548	AAGTAACCTCTCCAC[A/G]CAGAAGTTCCTGCCA	1102
rs189486101	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48494388	AGTCTATTATACTAA[C/T]TTAGGGTACAGCAAT	1102
rs189663470	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48507026	GGTAGCCTCTGCCCC[C/T]AGAGCAGCTGGTGAC	1102
rs189917050	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48492390	TGAGTCATTTGCATC[A/G]TTAGACAAGCTTCCA	1102
rs189927284	snp	A/C	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48514135	TTCTCTTTGGCATAT[A/C]CAAATTGCAAGCATC	1102
rs189933589	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48495227	ATCATAACAATACAT[A/G]GTCACTGTAAAAGTT	1102
rs190220741	snp	C/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48504449	ATACATGGTTGTTCA[C/G]GAATGTTCTTTCTCT	1102
rs190279179	snp	A/G	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48525970	GGGGAAGTTTTGGTG[A/G]AGGGAATACCAAAGA	1102
rs190281687	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522818	CATCAGAACATTTTA[C/T]CTGGTATTTTCTACA	1102
rs190292809	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48517231	CAGGAGGACAGAGAC[C/T]GAGTCTTTCACCACC	1102
rs190524242	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48529100	TTTTCAGCCACACAC[A/G]GCAAAAGTGTCATTT	1102
rs190532004	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48502009	GCAATGGATTTTTTC[C/T]CCTGAAGACAGATTT	1102
rs190566533	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48508750	TAACTGCAGTTTAAG[A/G]AGACAGAAATGCAAT	1102
rs190738449	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48528512	AAATTAAATAATATC[A/G]ATATCTTTTAGGGTA	1102
rs190790939	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534924	GTACCTGTGCACTCT[A/G]TTCCTTCCCATTACT	1102
rs190962273	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535114	GCATATTAACATTGC[A/G]CAACATTTGCCTATC	1102
rs190983601	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48492637	TCAGTCCTCGTGCAG[A/G]CGTGCCAGCAGCATC	1102
rs190997966	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514655	TAAATTCAAGGGTTG[A/G]GATTTCTTGGACCGT	1102
rs191124561	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48526364	AACATAGGAAGACAC[C/T]GTCTCTACAGAAAAC	1102
rs191155443	snp	C/T	0.00597247	0.0543191	downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488640	CAGCAGGGAAGGCTG[C/T]GCATGTGTAGGGCAT	1102
rs191161764	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48509776	GGTTCTTCATTTTCA[C/T]TGTTAAGTATTCCAG	1102
rs191215864	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48520822	GAGAATCAAAATTAC[A/G]TTAGGCATACCTAGC	1102
rs191273377	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48508917	AAGCCTTGGGTGATC[A/G]TTCTGGATCAGGGAC	1102
rs191284335	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48513223	GGCCACTTAACTCCC[C/T]TAGGTCTTAATTTCC	1102
rs191293822	snp	A/C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494017	TTGTAGTTAAACATG[A/C/T]GGTTTTAAAATGTGC	1102
rs191299766	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48515498	GCTTTTTTTTTTAAC[C/G]TTTTATTCCTTAGTT	1102
rs191606637	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48522348	GAAAGTTCCAAATCA[C/T]GGGGAAGAGCGGACA	1102
rs191614300	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534664	TAAAAGAATGTGTTT[A/C]ACTAAAGATTTTAAT	1102
rs191619828	snp	C/G	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48491707	TGGGCAGTTTGATGC[C/G]TCACAGATCTGGACA	1102
rs191643564	snp	A/G	0.00398564	0.0444627	intron-variant	RCBTB2	GRCh38.p7	13:48498716	GCCTGGGCAACAAGA[A/G]TGAAACTCTGTCTCA	1102
rs191672048	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48498046	CATAATTGGCCTTGA[A/G]GCCACATGTGTGGGT	1102
rs191880687	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48521259	TGCCATCTTTGTATA[C/T]AATGCTGGCTTTGCA	1102
rs191992451	snp	A/C	0.00597247	0.0543191	intron-variant	RCBTB2	GRCh38.p7	13:48527307	TGTTTGTTTTGGGAT[A/C]TATGACTTGGCTCAT	1102
rs192010450	snp	C/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48506479	GGCCAACCCAAGCTA[C/G]GTTGCCAAGGAGTAA	1102
rs192123271	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503252	TAGTGGTCCCCCCTA[A/C]CAAAAAAGGGTGGTT	1102
rs192243601	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48531288	AAAAATATCTCTGGA[A/G]TAAGTTAGTTTCCAA	1102
rs192258598	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489139	AATTTGTTTTGATCT[A/G]AAAAGTACAAATTTA	1102
rs192405814	snp	C/T	0.00279162	0.0372561	intron-variant	RCBTB2	GRCh38.p7	13:48497226	CTGGATCATTTTTCC[C/T]GACTTCCAAATGTTT	1102
rs192418075	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48505105	ACAAAAACTGGGTTT[A/G]AATCCTCGCTCTACC	1102
rs192471261	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48530658	ATCCACAGTCAGAGG[A/G]ACATTTAGAAGCAAT	1102
rs192491996	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48516264	TTGGTGGGTTTCCTC[A/G]TCCCTCAAGGAAGTT	1102
rs192629615	snp	A/C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532613	TTAGGATGAGAGCGG[A/C/T]CTCCGAGCAGATGAT	1102
rs192693021	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489861	GTGACTCAAAAAGAG[A/G]AAATGGTAAATAAGA	1102
rs192774779	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48515105	TATCCAAAACATAGT[A/C]AATTTCACAGGAAGA	1102
rs192906941	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48511020	TCACAGAAATCAAGG[A/G]GTATGAGGGGAATGT	1102
rs192914403	snp	C/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48502077	TATCTGCTTATAAAT[C/G]TGGCAAAATAACAAG	1102
rs193059758	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526613	CAGAGCAAGACTCTG[C/T]CTCTAAGAAAATAAA	1102
rs193094957	snp	A/G	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48494558	CCTGCCATGCCTCAA[A/G]GAGCTTACTTTCTAG	1102
rs193171565	snp	G/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48522948	TATTAGTAATTTTTT[G/T]CCTCAGCTATAAAAA	1102
rs193247728	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48505789	TGAGGGGGAACAGGA[C/T]ACAGGCAGCAATCCT	1102
rs193288647	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48500867	TTGATGTGATATAGA[A/G]AGAGTGAGCAAACGC	1102
rs199580568	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48530194	GGTGAGCCACCGCGC[C/G]CGGCCTGATTTGTAG	1102
rs199601338	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48493359	TCTTCTCTCTCTCAC[C/T]CTCTCTCTCTCTCCC	1102
rs199638083	snp	C/T	0.00199792	0.0315431	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512744	CTCTCCATCAGATGT[C/T]AGCACCAAAGAATGG	1102
rs199672673	in-del	-/CTC	0.0402882	0.136092	intron-variant	RCBTB2	GRCh38.p7	13:48527427	TCTTTGCAAAACAGT[-/CTC]CTATGTTATTTCCTC	1102
rs199723213	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535159	TTGATTATATGTCCC[A/G]TATCAGCTACCAATG	1102
rs199781376	snp	A/G	0.000462466	0.0151993	intron-variant	RCBTB2	GRCh38.p7	13:48521880	ACACATGCTCCAAGG[A/G]CATGATTTTTTTCTA	1102
rs199784122	in-del	-/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503545	TAATTCTCAGAACAA[-/T]TTTTTTTTTTTAAGA	1102
rs199842032	snp	C/T	1.68655e-05	0.00290387	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496263	GCCTTGCTTGATAGT[C/T]TGTTGGCAGAGCTTT	1102
rs199845827	snp	A/G	3.30677e-05	0.00406605	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502776	AAAGCAGGCAAACAC[A/G]TCGTCAGTGCAGGAG	1102
rs200179900	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516699	CTGTACTTCAACACA[C/T]AAATGTTGCAGGGTC	1102
rs200211132	in-del	-/GGCA	0.0166325	0.0896639	intron-variant	RCBTB2	GRCh38.p7	13:48532704	TGGGCCGGCGGCCTG[-/GGCA]GGCAGGATGTAGTCG	1102
rs200250178	snp	A/C			utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489606	TTTTAAGTTTATTTT[A/C]TGAAAGTTATTCCTT	1102
rs200254911	snp	G/T	1.6651e-05	0.00288535	intron-variant	RCBTB2	GRCh38.p7	13:48490272	AACAACAACAAAGAT[G/T]GTTTAATAAATTCAT	1102
rs200255608	snp	C/G/T	0.00875628	0.0656872	intron-variant	RCBTB2	GRCh38.p7	13:48527337	TATATATATATATAT[C/G/T]ATATATATATATATG	1102
rs200274959	snp	C/T	1.65004e-05	0.00287227	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502806	GAAGTGGGTGAGGTG[C/T]GGGAGGATCACGGAC	1102
rs200353992	snp	C/G	0.00199802	0.0315439	missense, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510716	GAATTGGCGCCCCAA[C/G]CATACACTTGGCCTT	1102
rs200382381	snp	C/T	1.70539e-05	0.00292005	intron-variant	RCBTB2	GRCh38.p7	13:48512932	ATCAGTTTTTTACAA[C/T]ATCTACTTCATTATA	1102
rs200525433	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48510646	GTCCTTTTCCACAGT[A/G]ACAGGAGTAGGATAG	1102
rs200532921	snp	A/G	0.000523659	0.0161727	intron-variant	RCBTB2	GRCh38.p7	13:48496158	GGTTCCATTTCTCCA[A/G]GAGGCCGGCAGCTGG	1102
rs200721128	snp	A/G	0.00478285	0.0486677	intron-variant	RCBTB2	GRCh38.p7	13:48521855	TGAAGTATGTTTCAT[A/G]CAACAGAACACACAT	1102
rs200728191	in-del	-/A			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502516	AAAGAAAAAAAAAAA[-/A]GTAGTCAAATAAAAT	1102
rs200758614	snp	C/T	0.00199792	0.0315431	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512757	GTTAGCACCAAAGAA[C/T]GGTAAGACCCACAGG	1102
rs200765786	snp	C/G/T	3.30863e-05	0.00406719	synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515712	TCCCACATCTAACAT[C/G/T]TTCAAAGATGACAGA	1102
rs200885019	snp	A/G	8.24002e-05	0.0064182	intron-variant	RCBTB2	GRCh38.p7	13:48510622	ACTGTGAAAATGCCC[A/G]TGTTACCTGTCCTTT	1102
rs200942045	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534640	AGTTAAAACTTTAAA[A/G]TATACCTATAAAAGA	1102
rs201034805	snp	G/T	0.00199792	0.0315431	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499719	CTCATTTCTACAATA[G/T]CATCCTCGTTATCTT	1102
rs201092222	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48527353	ATATATATATATATG[A/T]TATATATTTATATAT	1102
rs201107003	snp	C/G/T	0.000877781	0.0209318	intron-variant	RCBTB2	GRCh38.p7	13:48511921	TCAAGAGACAAATGG[C/G/T]CAGCAAGCTGTCTGT	1102
rs201108130	snp	C/T	3.29603e-05	0.00405944	intron-variant	RCBTB2	GRCh38.p7	13:48510621	GACTGTGAAAATGCC[C/T]GTGTTACCTGTCCTT	1102
rs201142463	snp	A/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502663	CTCATTATCAAAGTA[A/G]AGCCCTGAGCTCTTT	1102
rs201180519	snp	G/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48524077	ATACTATTAAAAAGT[G/T]TTTTGAATTTTTTAG	1102
rs201190377	snp	A/T	0.256619	0.249912	intron-variant	RCBTB2	GRCh38.p7	13:48527361	ATATATGATATATAT[A/T]TATATATGATATATA	1102
rs201227068	in-del	-/A	0.00557542	0.0525036	intron-variant	RCBTB2	GRCh38.p7	13:48528298	ACAGAAGAAGGGGTG[-/A]AAAAAAATAGCAATT	1102
rs201249325	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48517760	TTTTCTGAGAAACCC[A/G]AAGAAACCCCAGAGA	1102
rs201264399	in-del	-/TAT			intron-variant	RCBTB2	GRCh38.p7	13:48518478	AAAAAAAAAAATATA[-/TAT]ATATATATATATATA	1102
rs201305132	in-del	-/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535144	CTTTTAAAAAGTTCC[-/T]TGATTATATGTCCCC	1102
rs201477264	snp	A/G			synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490150	GCTTGCTTTGCTGAT[A/G]AAGTTCTTCAGGAGA	1102
rs201503910	in-del	-/C	0.0178098	0.0926698	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503467	TGGAGCCCAGGAGAG[-/C]CAGTTTCCTAGGATC	1102
rs201566957	snp	G/T	0.00179545	0.0299082	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515323	GTCACCTAACCCCAA[G/T]CAGCCACAGCAGTTT	1102
rs201714440	snp	A/G	1.66785e-05	0.00288773	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501858	AGCCACTGTGAGGTG[A/G]TCATCAGGTTCTAGG	1102
rs201775073	snp	C/T	3.76875e-05	0.00434077	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502932	AAATTCACAAACACA[C/T]ACCACATAAGCACAG	1102
rs201796149	snp	A/G	0.000148614	0.00861887	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48521920	CTGTCTCCAGAGAAA[A/G]GAGGAAGTTCTTCTT	1102
rs201960216	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48527369	TATATATTTATATAT[C/G]ATATATATATATGAT	1102
rs201996822	snp	C/T	9.89805e-05	0.00703423	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499746	TCTTCCAATGACGAA[C/T]GAAAATGCTCACATC	1102
rs367625524	snp	A/G	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48500813	GGGCCATAGTACTGT[A/G]TTACAGCAAACAAAT	1102
rs367684064	snp	A/C/T	3.33958e-05	0.0040862	intron-variant	RCBTB2	GRCh38.p7	13:48512180	AGGCAAATACCTGTT[A/C/T]AAAGGAAAGATCAGT	1102
rs367705717	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529427	ATAATACAGGACATA[C/T]TATAATGCAGTCAAA	1102
rs367772205	in-del	-/GAGAA			intron-variant	RCBTB2	GRCh38.p7	13:48523662	GAAAGAGGGAGAGAA[-/GAGAA]AAAAGAAGGGACCAA	1102
rs367818579	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529515	CCATAGGGAGATATA[C/T]ATAAGAGATATTAGC	1102
rs367863595	in-del	-/AA	0.00023165	0.0107597	intron-variant	RCBTB2	GRCh38.p7	13:48511908	ACCCTCAATCCTCTC[-/AA]GAGACAAATGGCCAG	1102
rs367868760	snp	C/G	0.000153988	0.00877328	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502945	CACACCACATAAGCA[C/G]AGTGACCGGGGCAGA	1102
rs368056169	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533495	CCCAGCTTTTCTTCT[A/G]TTGCTGGCCCCTCTA	1102
rs368227859	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48504910	TGTTCTCATGTGCGG[C/T]AATCTCACTGACTTA	1102
rs368326717	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48526552	TAAAAAATAAATAAT[G/T]TTTTTAATGAGCTAT	1102
rs368358334	snp	A/C/T	3.30542e-05	0.00406524	intron-variant	RCBTB2	GRCh38.p7	13:48521870	GCAACAGAACACACA[A/C/T]GCTCCAAGGGCATGA	1102
rs368376267	snp	C/T	0.000153988	0.00877328	intron-variant	RCBTB2	GRCh38.p7	13:48512690	GTCTACATAATCTTA[C/T]TGAAAAAAATCAATG	1102
rs368462354	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499712	AAATTCACTCATTTC[C/T]ACAATATCATCCTCG	1102
rs368714123	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48499868	TGGCACGTCCCTGCT[A/G]TGGCTCCTCACTTTC	1102
rs368746579	snp	A/C	1.64866e-05	0.00287106	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515236	AATATGTGGACCACT[A/C]CCATAGCTGAGGCAG	1102
rs368814361	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533348	CCAGGGAGTTCCTCC[A/G]TGGGTCACCCCCACC	1102
rs368856589	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48511539	TTAAGCTTCCTCAGG[A/G]AAGCTTGTAACAATT	1102
rs368955568	snp	C/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48526367	ATAGGAAGACACCGT[C/T]TCTACAGAAAACTTA	1102
rs369016397	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48516358	AAAGTAGTGACAAAC[A/G]AGGTGGCTTAACCAA	1102
rs369058000	snp	A/C	1.65312e-05	0.00287495	splice-acceptor-variant, intron-variant	RCBTB2	GRCh38.p7	13:48510772	GTAGCCACAGGCGAC[A/C]TGGAAGGAAAAAAAT	1102
rs369075672	snp	C/T			downstream-variant-500B	RCBTB2	GRCh38.p7	13:48488864	TGCTTGATAAGAGCA[C/T]AATATATCCAATTTA	1102
rs369101043	snp	C/T	0.000175282	0.00936003	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48502705	AGGCCATCCCCCAAA[C/T]GGACAGTGACCAGCT	1102
rs369329602	snp	A/C/G	1.69968e-05	0.00291515	synonymous-codon, downstream-variant-500B, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502731	CAGCTTACCCACGGA[A/C/G]AGGAGGCGCCACGTG	1102
rs369357506	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48490640	TATATTTATATCAGC[A/G]TCTTTAAGTATGTCT	1102
rs369373114	snp	A/G	1.67396e-05	0.00289301	intron-variant	RCBTB2	GRCh38.p7	13:48510810	GGACTGCAAATATAA[A/G]TAATTATTTCACTGC	1102
rs369460161	snp	A/G	1.64838e-05	0.00287083	intron-variant	RCBTB2	GRCh38.p7	13:48510610	ACCAGTGTGGGGACT[A/G]TGAAAATGCCCGTGT	1102
rs369465761	snp	C/T	0.00139503	0.0263736	intron-variant	RCBTB2	GRCh38.p7	13:48510577	TATCTAAGTCCTGTT[C/T]AATCACAATCACCAA	1102
rs369472476	in-del	-/CAGG			intron-variant	RCBTB2	GRCh38.p7	13:48532710	GGCGGCCTGGGCAGG[-/CAGG]ATGTAGTCGCGAGCA	1102
rs369587919	in-del	-/C			frameshift-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515323	TCACCTAACCCCAAA[-/C]CAGCCACAGCAGTTT	1102
rs369593207	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491376	ACTGGGCAGGCTGTT[A/G]GTACCACACCAGCAA	1102
rs369594536	snp	A/G	0.000153988	0.00877328	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490080	TTTGCAGGGGAAATG[A/G]AAAGGCTCAAAAACT	1102
rs369663278	snp	C/G/T	4.95184e-05	0.00497562	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515626	ACTTCATTGCCAGCA[C/G/T]TGCCAAAGACACAAG	1102
rs369737935	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508405	CTCATTTAAAACATT[C/T]ATCCATGTTTTTTTT	1102
rs369741042	snp	A/T	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48523825	TTTCAGTGTCTTTTA[A/T]CAATTTCAAGTAAAA	1102
rs369861410	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48496887	ATGGACACGTGTCTT[C/T]CTCCTGTTACCCTAT	1102
rs369939077	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48499412	CCTGCAATGCTCCAC[A/G]GTGGTGATGATTTGA	1102
rs369951741	snp	A/T			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503231	TTCAAGTATAACCCA[A/T]GAGAGTAGTGGTCCC	1102
rs370124110	snp	A/C/T			intron-variant	RCBTB2	GRCh38.p7	13:48525318	TATAAAGAATGCCTG[A/C/T]AAATCAGTAAGAATA	1102
rs370148586	snp	C/T	0.000206118	0.0101497	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496297	AAACGATTTTCTCTA[C/T]AAAATGTAGCCAAGT	1102
rs370178844	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48498326	GACATATTTTTATCT[G/T]AAGTTCACTAGCTTG	1102
rs370223570	snp	A/G	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512087	CTACTTTATTTTGTA[A/G]GCAGCCAGTGACTCT	1102
rs370339278	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526200	ATAAACGTTTGGTAA[C/T]GAAAACTCATAAACT	1102
rs370374256	snp	A/G	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48532747	CGGGCCCACGCCAGC[A/G]GAATTGCGCATGCGC	1102
rs370408375	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48491814	TTTATTCTAGAGTGG[A/G]ATCTTCCCCTAAATA	1102
rs370436397	snp	G/T	0.00478085	0.0486577	intron-variant	RCBTB2	GRCh38.p7	13:48518895	CTTCGTTTTTAATTT[G/T]TTTCCTATTTTAAGT	1102
rs370437070	in-del	-/CCACACACACACACACACACACACACA			intron-variant	RCBTB2	GRCh38.p7	13:48493289	ACCCTCTCTCTCTCT[-/CCACACACACACACACACACACACACA]CTCTCTCTCTCTCTC	1102
rs370486023	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48510825	GTAATTATTTCACTG[C/T]TTCCACAAAGTAGGT	1102
rs370601264	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48513788	TGATATTTAGTAATC[C/T]GTTCTTGCTGTCTGT	1102
rs370634938	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48499662	ATGCTGTCTGTGTAT[A/C]GGTATTCCAGGAAGG	1102
rs370686534	snp	C/G/T			utr-variant-5-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48533040	TACCTCCTCGCAGGC[C/G/T]GGAGCCTTGTCCGCT	1102
rs370708257	snp	A/G	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48500785	CCAGAACTTTATGTT[A/G]CTTAAGCCACCCGGG	1102
rs370784246	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48527061	ATTAAAATGGCAAAA[A/G]TGTGCTTTCTACTTA	1102
rs370938189	snp	A/G	0.000110365	0.00742768	intron-variant	RCBTB2	GRCh38.p7	13:48511745	GACTTAAAAATACAC[A/G]CACACAAACTGACAG	1102
rs371016980	snp	C/G/T	0.000166273	0.00911658	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48511780	CGTACCCTCTGGACA[C/G/T]GGATGCCTTGCAAAG	1102
rs371439325	snp	C/T	3.30077e-05	0.00406236	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502850	GGCCCCACATGTACA[C/T]GTGCCCACCCTGCGT	1102
rs371609964	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532113	TATAGTCCTGGTCTC[A/G]AACTGTTGCAACATT	1102
rs371615778	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48520436	TGTCCCTAGAATTCA[C/G]TCCTGGTTTGGCACA	1102
rs371651988	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48514278	CGGGTGGGAGTGTCT[A/G]TGGCAGAGATGCTGG	1102
rs371684107	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48505168	ACTAGGGGAATGTCA[C/T]TTAGCACCTAGGAGC	1102
rs371704336	snp	A/C/T	3.39462e-05	0.00411973	missense, utr-variant-3-prime, intron-variant, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502901	TGGAGTGACAGGCTG[A/C/T]AATCTCGATAATCCT	1102
rs371709025	snp	A/G	0.000153988	0.00877328	intron-variant	RCBTB2	GRCh38.p7	13:48512196	AAAGGAAAGATCAGT[A/G]AATGAAACAGATTAA	1102
rs371768944	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514882	AATGCTAAGAGTTGG[C/T]GGGGGGATGTTGGAC	1102
rs371775666	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48490209	TTTGTGTTACTACAG[A/T]CAGATGGTTTATGCA	1102
rs371776463	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48521374	GATATTATGTAAATT[-/T]AACAAAATAACACAA	1102
rs371792631	snp	A/G	0.00052322	0.0161659	intron-variant	RCBTB2	GRCh38.p7	13:48501877	TCAGGTTCTAGGAGA[A/G]TAATGCAAATGCTTC	1102
rs371840036	snp	A/T	3.33439e-05	0.00408299	intron-variant	RCBTB2	GRCh38.p7	13:48512691	TCTACATAATCTTAT[A/T]GAAAAAAATCAATGA	1102
rs371916892	in-del	-/ACTTCTTCCTTCCTGTTTCGC			intron-variant	RCBTB2	GRCh38.p7	13:48492686	TCCTTCCTGTTTCGC[-/ACTTCTTCCTTCCTGTTTCGC]TTTCTTTCCCAGCCT	1102
rs371947280	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48494154	TGCCTATGTCATATA[A/T]GGTTGTTTTGAGGAG	1102
rs372032127	snp	C/T	0.00199481	0.0315187	intron-variant	RCBTB2	GRCh38.p7	13:48498458	ACTCGCGGCCGGGCG[C/T]AGTGGCTCACGCCTG	1102
rs372243933	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48511477	TTGTTGGTTCCTCAG[C/G]GAAATTCCCTAGGAG	1102
rs372271541	snp	A/G	0.00029299	0.0121	intron-variant	RCBTB2	GRCh38.p7	13:48512937	TTTTTTACAACATCT[A/G]CTTCATTATACGAAA	1102
rs372400393	snp	A/C/T	7.08797e-05	0.00595278	intron-variant	RCBTB2	GRCh38.p7	13:48496326	GTCTAGCAGTCCTGG[A/C/T]GGAAAGAGGTGTTTA	1102
rs372463880	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48489055	CCTTTACATTACATG[A/G]CATTGTGAGATACAC	1102
rs372469541	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48514926	TTTCAATTCATAGAT[C/T]AAGAATCCAAAGTTC	1102
rs372505294	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48516738	CCCCCTAACAGCATA[C/T]ATTAAGATCACGAGC	1102
rs372568472	snp	A/T			intron-variant	RCBTB2	GRCh38.p7	13:48504471	TCTTTCTCTCTGCCT[A/T]ACAAACCCTACCCAT	1102
rs372650887	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48498548	CCAGCCTGACCAACA[C/T]GGAGAAACCTCGTTT	1102
rs372672305	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48534712	GTTTTTCCCAGGGCG[A/G]TCAAAATTAAAAGTA	1102
rs372873209	snp	A/G	6.59674e-05	0.00574277	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515641	CTGCCAAAGACACAA[A/G]CCTGACGAATTAACT	1102
rs372907752	snp	C/G/T	0.000137765	0.00829861	splice-donor-variant, downstream-variant-500B, intron-variant	RCBTB2	GRCh38.p7	13:48502723	ACAGTGACCAGCTTA[C/G/T]CCACGGAGAGGAGGC	1102
rs372933456	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48511268	TACCATTACACATAG[C/T]AGTTTTCCATGTCAT	1102
rs372942386	snp	A/C	0.000200237	0.0100039	intron-variant	RCBTB2	GRCh38.p7	13:48510801	ATCCACTCAGGACTG[A/C]AAATATAAGTAATTA	1102
rs373038751	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532666	CGACCCCTACCAGAG[A/G]ACTCGCGCATGCGCA	1102
rs373082263	snp	C/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48508435	TTTTTTTGAGACAGA[C/G]TCTCACTCTACTGCC	1102
rs373134067	snp	C/T	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48509877	AATATAATAAAGATA[C/T]ATGCAGTAAAAACAG	1102
rs373380665	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48516724	AGGGTCACAATTAAC[A/C]CCCTAACAGCATACA	1102
rs373421828	snp	A/G	5.07997e-05	0.00503957	intron-variant	RCBTB2	GRCh38.p7	13:48501882	TTCTAGGAGAATAAT[A/G]CAAATGCTTCCAGAG	1102
rs373503489	snp	A/C/G	0.000230869	0.0107417	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515642	TGCCAAAGACACAAG[A/C/G]CTGACGAATTAACTG	1102
rs373552083	snp	A/G	3.48596e-05	0.00417476	missense, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496216	TACTTCACCGCAGCC[A/G]AGAGCAGAGCGATGG	1102
rs373643779	in-del	-/TT			intron-variant	RCBTB2	GRCh38.p7	13:48493224	TCCTAAGTACCCTCC[-/TT]CACACACACACACAC	1102
rs373752194	snp	C/G	7.96876e-05	0.00631169	intron-variant	RCBTB2	GRCh38.p7	13:48511725	TTGATATCTTTGCCA[C/G]CGAAGACTTAAAAAT	1102
rs373914407	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48535113	AGCATATTAACATTG[C/T]GCAACATTTGCCTAT	1102
rs373929704	snp	C/G	1.6483e-05	0.00287076	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48515252	CCATAGCTGAGGCAG[C/G]CTATTTTTTTGCCAT	1102
rs373952680	snp	A/C	1.66671e-05	0.00288674	intron-variant	RCBTB2	GRCh38.p7	13:48490277	CAACAAAGATGGTTT[A/C]ATAAATTCATATTTA	1102
rs374054544	snp	C/T	3.98613e-05	0.0044642	intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48502935	TTCACAAACACACAC[C/T]ACATAAGCACAGTGA	1102
rs374055598	snp	A/C			intron-variant, utr-variant-3-prime	RCBTB2	GRCh38.p7	13:48503443	TTCTACCACACTGGG[A/C]TGTATGACCTGGAGC	1102
rs374097079	snp	C/T	0.000798403	0.0199641	intron-variant	RCBTB2	GRCh38.p7	13:48497457	CTCTAATTGAAGCAG[C/T]CAATCAGCATCTGAA	1102
rs374152919	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48530695	AACTGTGGAGACAAC[A/G]TACAGTTTTTCTCAG	1102
rs374169554	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48511357	TAATCATTAACTTAC[A/G]ATTTGATTAGTAAAT	1102
rs374388911	snp	A/G	5.39224e-05	0.00519214	intron-variant	RCBTB2	GRCh38.p7	13:48496346	AGAGGTGTTTATTAG[A/G]GGGAGTGATTTCAAG	1102
rs374434842	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532933	TCGGGCCGCAGGGGC[A/G]GGGAGGGGTGGCCTG	1102
rs374478911	snp	C/T	3.2956e-05	0.00405918	missense, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48512104	CAGCCAGTGACTCTT[C/T]GAGGGATTGGCTGAT	1102
rs374595662	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48531820	ATCATATAAGATTAC[A/G]AAGCACAGAGTAATG	1102
rs374839378	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48505642	AGCAAATGTGAGGAT[A/G]GCGACATGGTCTGTC	1102
rs374863544	snp	A/C	0.000399281	0.0141238	intron-variant	RCBTB2	GRCh38.p7	13:48498062	GCCACATGTGTGGGT[A/C]TTTCCTCCCTTAGAC	1102
rs374927238	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48525696	CAAAAAGCAAGAAAG[A/G]ACAAATTGATCAACA	1102
rs375015612	snp	A/G	0.00159617	0.0282053	intron-variant	RCBTB2	GRCh38.p7	13:48500798	TTGCTTAAGCCACCC[A/G]GGCCATAGTACTGTG	1102
rs375265001	snp	A/C	0.000153988	0.00877328	intron-variant	RCBTB2	GRCh38.p7	13:48510598	CAATCACCAAAGACC[A/C]GTGTGGGGACTGTGA	1102
rs375273668	snp	C/T	0.00119737	0.0244387	intron-variant	RCBTB2	GRCh38.p7	13:48522648	GGTTTAATCATTATG[C/T]AGTTAACGATTTCAT	1102
rs375367937	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48515872	TTTTGAGAGGCCTCT[C/T]GCAGCTGCAGGGATT	1102
rs375378897	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48529045	TACAAAGCAAAGCGG[C/T]ATTTAATTGAAAAGA	1102
rs375600248	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48505140	GGCTGCGTGACTAGC[A/C]CTAGGCTGCGTGACT	1102
rs375690650	snp	C/G			intron-variant	RCBTB2	GRCh38.p7	13:48498934	AAATCCCATCAGCAA[C/G]CTCTTTAAAATATAT	1102
rs375709474	snp	A/G			upstream-variant-2KB, intron-variant	RCBTB2	GRCh38.p7	13:48533436	GATAAGGCGTGTATG[A/G]TGCTGAGAGCAACCT	1102
rs375971438	snp	A/G	0.000100985	0.00710508	intron-variant	RCBTB2	GRCh38.p7	13:48515167	CTCAAGGGCAGCTGC[A/G]AATAAAGCTGAAATT	1102
rs376033979	snp	A/G	3.30071e-05	0.00406232	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502851	GCCCCACATGTACAC[A/G]TGCCCACCCTGCGTC	1102
rs376073113	snp	A/C	1.69083e-05	0.00290755	intron-variant	RCBTB2	GRCh38.p7	13:48501880	GGTTCTAGGAGAATA[A/C]TGCAAATGCTTCCAG	1102
rs376154524	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48526304	TGTAATCCCAGCACT[C/T]TGAGGATCGCTTGAG	1102
rs376157246	snp	A/G			intron-variant, downstream-variant-500B	RCBTB2	GRCh38.p7	13:48501671	ACTGAGGTGCCTAAT[A/G]TAGTTGGACACTTAG	1102
rs376160546	snp	A/C			intron-variant	RCBTB2	GRCh38.p7	13:48495403	AATAAAAATAGGATA[A/C]GTTTTTCACTTAGTG	1102
rs376370151	snp	A/G	1.69172e-05	0.00290832	synonymous-codon, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48496248	ATTCTCCTCGCAGAT[A/G]CCTTGCTTGATAGTT	1102
rs376527428	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48532723	AGGATGTAGTCGCGA[A/G]CAGCGCACCGGGCCC	1102
rs376537349	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48530193	AGGTGAGCCACCGCG[C/T]CCGGCCTGATTTGTA	1102
rs376658265	in-del	-/A/C/CC	0.0305019	0.119669	intron-variant	RCBTB2	GRCh38.p7	13:48532570	TCGGGACCTGTGACG[-/A/C/CC]CCCCCAGCCACACCA	1102
rs376690025	snp	A/G	8.2715e-05	0.00643045	missense, utr-variant-3-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48501814	AGGTCTGCAGTGTCC[A/G]GGTTGTCAAATTCCC	1102
rs376730128	snp	G/T	0.000234532	0.0108264	intron-variant	RCBTB2	GRCh38.p7	13:48496165	TTTCTCCAGGAGGCC[G/T]GCAGCTGGAAGCAAG	1102
rs376734414	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48524075	TAATACTATTAAAAA[G/T]TGTTTTGAATTTTTT	1102
rs376814058	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48508469	GCTAGAGTGCAGTGT[C/T]GCGATCTCACTGCAA	1102
rs376814631	snp	A/G			intron-variant	RCBTB2	GRCh38.p7	13:48506303	AATCCAGAGCCGAAG[A/G]GTTCTGATTTGATCT	1102
rs377109846	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48517600	ACGGAGCAGCTGTCC[C/T]AATGGCCACTGGACC	1102
rs377216181	snp	G/T	1.65173e-05	0.00287374	intron-variant	RCBTB2	GRCh38.p7	13:48521883	CATGCTCCAAGGGCA[G/T]GATTTTTTTCTAACC	1102
rs377300504	in-del	-/AG			intron-variant	RCBTB2	GRCh38.p7	13:48531431	AACCAGCAGTACAAG[-/AG]TTTGGAGAGCCAGAC	1102
rs377458172	snp	C/T	0.000153988	0.00877328	intron-variant	RCBTB2	GRCh38.p7	13:48512013	GTAAAATAACTTCCT[C/T]ACCTCCCCCGTGTCT	1102
rs377460175	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48532138	AACATTTTATGTAAT[C/T]TTTGCAAAGAACAAA	1102
rs377639963	snp	C/T	8.24804e-05	0.00642132	missense, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502828	ATCACGGACTGACCC[C/T]GGCACTGGCCCCACA	1102
rs377664749	snp	C/T	3.30857e-05	0.00406716	synonymous-codon, utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	RCBTB2	GRCh38.p7	13:48502872	ACCCTGCGTCTTGGC[C/T]GCAGACGTGTGTGTG	1102
rs377670396	snp	A/G	0.000178333	0.00944111	intron-variant	RCBTB2	GRCh38.p7	13:48511727	GATATCTTTGCCAGC[A/G]AAGACTTAAAAATAC	1102
rs377734272	snp	C/T			intron-variant	RCBTB2	GRCh38.p7	13:48524397	GCACTAAGTGCCTCA[C/T]CTTATTTAATCTTTA	1102
rs377738244	snp	G/T			intron-variant	RCBTB2	GRCh38.p7	13:48497739	ATAAATCTTATACAT[G/T]TGGTAGACTTTGGTT	1102
rs386379119	in-del	-/CA			intron-variant	RCBTB2	GRCh38.p7	13:48502171	TTAAAAGTAAAAAAC[-/CA]AGTTTCTCAGTAAAA	1102
rs386770809	multinucleotide-polymorphism	ACC/CCT			intron-variant	RCBTB2	GRCh38.p7	13:48504419	CAGGCTTTCTCATTG[ACC/CCT]TTCAATGACTTCATA	1102
rs386770810	multinucleotide-polymorphism	AA/GG			intron-variant	RCBTB2	GRCh38.p7	13:48512462	TTTTCCAGCATTTGG[AA/GG]ATTTTTCTTATTGCA	1102
rs397723038	in-del	-/T	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48515494	CCATGCTTTTTTTTT[-/T]AACCTTTTATTCCTT	1102
rs397851428	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48518459	TACAGAGTACTTTGC[-/A]AAAAAAAAAAAAAAT	1102
rs397851588	in-del	-/A			intron-variant	RCBTB2	GRCh38.p7	13:48518460	ACAGAGTACTTTGCA[-/A]AAAAAAAAAAAAATA	1102
rs398022688	in-del	-/AGAG	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48516117	GAGAGAGAGAGAGAG[-/AGAG]CTGCCATGTCATCTG	1102
rs398022689	in-del	-/AA	0	0	intron-variant	RCBTB2	GRCh38.p7	13:48518472	GCAAAAAAAAAAAAA[-/AA]TATATATATATATAT	1102
rs398077259	in-del	-/T			intron-variant	RCBTB2	GRCh38.p7	13:48515493	TCCATGCTTTTTTTT[-/T]TAACCTTTTATTCCT	1102

Page 1 | 2