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

RNF34

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs8462	snp	A/G	0.3512	0.228601	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424268	TCACTATACAAAACA[A/G]TGTAAACTGATTACA	80196
rs750008	snp	C/G	0.0486741	0.148216	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419701	TTTGTGTTTTCTAAA[C/G]TGTTCTGATTGAGAA	80196
rs889970	snp	C/T	0.47852	0.101384	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418414	TGTCCAAGGACCTCA[C/T]TGGGACAATATTATT	80196
rs1110337	snp	A/G	0	0	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420730	AAATGGGAACTGGTA[A/G]AGAAAGTAAACCGGT	80196
rs1177625	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408270	tatttttagtagaga[C/G/T]ggggtttcaccatgt	80196
rs1177626	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408190	gcctcccaaagtgtt[A/G]ggattacaggcgtga	80196
rs1177634	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410070	acctcccaggttcaa[C/G]cgattctcctgcctc	80196
rs1182952	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408229	ggtctcgaactcctg[A/G]cctcaggtgatctgc	80196
rs1305816	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410142	tttgagacggagttt[C/T]gctcttgtcacccag	80196
rs1305817	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410125	ctcttgttgcccagg[C/T]tggagtgcagtggcg	80196
rs1612971	snp	A/C/G	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410916	CCAAGCCAACCTCCA[A/C/G]AGTGTCCCAGGCAAA	80196
rs1706458	snp	A/G	0.200182	0.244986	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413641	gcagtgagcccagat[A/G]gcaccactgcactcc	80196
rs1706459	snp	A/G	0.390277	0.206936	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413428	caaaactccgtctca[A/G]aaaaaaaaaaaaGGA	80196
rs2293462	snp	C/T	0.350982	0.228698	intron-variant	RNF34	GRCh38.p7	12:121401051	ACTTTCAGACCTAGA[C/T]GGTTTCGTTAATCTC	80196
rs2293463	snp	A/G	0.350764	0.228794	intron-variant	RNF34	GRCh38.p7	12:121401153	TCAAAGATTTACTAT[A/G]GAAGATTGAAAAAGA	80196
rs2552078	snp	C/T					GRCh38.p7	12:121415017	cgtccgcctcccggg[C/T]tcaagcgattctcct	80196
rs2668257	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415000	gctggggaggctgag[A/G]caggagaatcgcttg	80196
rs2668258	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415038	gaggcggacgttgca[G/T]tgagccgagatcacg	80196
rs2695150	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414937	agctaattttttgta[C/G/T]ttttggtagacacag	80196
rs3080027	in-del	-/TA/TAG	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419578	GTGCCTGGCAATCAG[-/TA/TAG]GGTGGAATATTTGAA	80196
rs3751132	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423998	GAGCCACTGCTCAGC[A/C]TGTTCCATGTCGGCC	80196
rs3751133	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422743	TAAGAAAGACGATGA[A/G]TAAGTTAAAAAAAAG	80196
rs3751134	snp	A/C	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420409	CCTGTACTAATCTAG[A/C]GAATGTCCACAGGGC	80196
rs3751135	snp	A/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420405	TACTAATCTAGCGAA[A/T]GTCCACAGGGCACTG	80196
rs3763973	snp	C/T	0.350764	0.228794	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399338	TATTTTTGACAAGGT[C/T]TTGCTCTTGCCCAGG	80196
rs3842646	in-del	-/T	0.351418	0.228505	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422916	GAGCCTTAGTTCCCC[-/T]CTTAGGAAAGTTAGG	80196
rs4081775	snp	C/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409776	TTTTAGTCCTGTACC[C/T]TCGTAGCTGCTGTCA	80196
rs4640009	snp	C/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422116	ATGTACAGTGCACAA[C/T]GATAATGCCATTCCC	80196
rs7132130	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410581	TGGGAAAAAAAAAAA[A/T]ACTTCAAATATACTA	80196
rs7296507	snp	A/G	0.478603	0.101197	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409332	ACCAAAGTGGGATGC[A/G]AAATACTACATATCC	80196
rs7301132	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410410	ggtgtggtggtgggt[G/T]cctgtaatcccggct	80196
rs7311543	snp	A/C	0.350982	0.228698	intron-variant	RNF34	GRCh38.p7	12:121400757	ACGTCGGGGCCGCGA[A/C]CTAGAGAAGGCTGGA	80196
rs7311592	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421684	ttatttttttctttt[A/T]aattgtaaaaaaaat	80196
rs7311596	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421690	ttttctttttaattg[A/T]aaaaaaaatatatat	80196
rs7311769	snp	C/T	0.029116	0.117091	intron-variant	RNF34	GRCh38.p7	12:121400818	CAAGGAATTTGGCAG[C/T]TTGAGTTCTCCAAGG	80196
rs7961800	snp	A/G	0.00597247	0.0543191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422024	GAGCTTTCAGAGGTC[A/G]TAGGCTGCTGGCTGG	80196
rs10744761	snp	C/T	0.492727	0.0598633	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398223	TAAAAATACAAAAAA[C/T]TAGCCGGGCGCGGTG	80196
rs10744762	snp	A/C	0.492435	0.0610346	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401898	GACATCAGCCTGTGC[A/C]AGATGACAGTTATAA	80196
rs10774594	snp	A/G	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404917	CTTGAGGCCATTTGA[A/G]AATCCTGGCACTGTG	80196
rs10849875	snp	A/G	0.415891	0.18703	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398176	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG	80196
rs10849876	snp	A/G	0.479014	0.100263	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398302	gcgtgaacccaggag[A/G]cggagcttgcagtga	80196
rs10849877	snp	A/G	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404465	GGTGGCACCATCTCA[A/G]CTTACTGCAGTCTCC	80196
rs10849878	snp	A/G	0.417196	0.185864	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406489	ATGGCGTTTCACCAC[A/G]TTGCCCACGCTGGTC	80196
rs10849879	snp	A/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411512	TTGTATTCTTCCCTA[A/T]TTCATTGTAAAACTA	80196
rs10849880	snp	A/C	0.416708	0.186302	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422041	AGGCTGCTGGCTGGG[A/C]AATGGTTTTCTGGCA	80196
rs11065555	snp	A/T	0.444444	0.157135	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398385	TCAAAAAAAAAAAAA[A/T]TTTTTTTTTTAAGAA	80196
rs11065556	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398614	TTAACTCTGGAGGTA[A/G]ACCTGCCAGGCCTTT	80196
rs11065557	snp	A/C/G	0	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398664	GGCTTTGTACCCCAA[A/C/G]AACATTTTTATTGAG	80196
rs11065558	snp	A/G	0.00649344	0.0566088	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398813	GACTATTATGGATAA[A/G]AAGTGACATTATCTG	80196
rs11065559	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404658	AAAGTGCTGGGATTA[A/G]AGGTGTGAGCTACTG	80196
rs11065560	snp	A/G	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407760	AAGAACATGAACTTA[A/G]GTCTCTAAAGCTTTT	80196
rs11065561	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412169	TGGGTTCAAGCGATT[C/T]TCCTGCCTCAGCCTC	80196
rs11065562	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413101	TGCGATCTAGGCTCA[C/G]TGCAACCTCCGCCTC	80196
rs11065563	snp	C/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413466	GCCCAAGCTGGAGTG[C/T]GGTGGCACAATCTTG	80196
rs11065564	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414327	GGCAAAAGCCTATTC[A/G]TTCTAAACACTATAG	80196
rs11065565	snp	C/T	0.445196	0.1562	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415361	CATAGTGGCTCACAC[C/T]TGTAATCTGAGCACT	80196
rs11065566	snp	C/T	0.478354	0.101757	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415570	GCAGTGAGCCGAGAT[C/T]GCGCCACTGTACTCC	80196
rs11065567	snp	C/T	0.01233	0.0775433	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421247	TGAGGTTAAGAACTT[C/T]TGAACTAggctgggc	80196
rs11398833	in-del	-/A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421372	GAGATCCCATCTCTA[-/A/C]AAAAAAAAAAAAAAA	80196
rs11446752	in-del	-/A			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424725	AAAAAAAAAAAAAAA[-/A]GAAAAAAAAGAAAAA	80196
rs11545004	snp	A/G			intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417600	CACTTATTACAAGAG[A/G]CAGCATTTCAGCGCC	80196
rs11545005	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424187	TGTTCAGGTATAGCT[C/T]TTTATAGCAAGGGCT	80196
rs11610134	snp	A/G	0.00934559	0.067716	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417375	CATGAAAATACCTCT[A/G]GAAATAGTCTGGTGC	80196
rs11612856	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412706	TAAATTAACTCTTAG[G/T]GAATCTAGATGTTCA	80196
rs11615530	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401872	TCAGAAGCAAAATAT[A/G]GACCTGAATAGACAT	80196
rs11829166	snp	G/T	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404784	TTAAAAGTTTAGGGT[G/T]GAAAATTTGTGGTAA	80196
rs11830100	snp	A/G	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410150	caagagcgaaactcc[A/G]tctcaaaaaaaaaga	80196
rs11830307	snp	A/T	0.34659	0.230587	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398384	CTCAAAAAAAAAAAA[A/T]TTTTTTTTTTTAAGA	80196
rs11831204	snp	C/T	0.350764	0.228794	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408206	AACACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA	80196
rs11831315	snp	C/T	0.245452	0.249959	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402831	TGTATCTATAGCACA[C/T]GTTATTGTAATAATC	80196
rs11833355	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408127	CCTGGGCAGCATATC[A/G]AGACCCCGTCTCTAA	80196
rs11837988	snp	C/T	0.350764	0.228794	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398486	TCCACATCCTCACCA[C/T]CTATTTTCTTTCTTT	80196
rs12099579	snp	A/G	0.184838	0.241358	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412187	CTGCCTCAGCCTCCC[A/G]ACTAGCTGGGACTAC	80196
rs12314670	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404415	tttttttttttttga[A/G]atggagtctctcttt	80196
rs12321719	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404417	tttttttttttgaga[A/T]ggagtctctctttgt	80196
rs12368549	snp	A/T			intron-variant	RNF34	GRCh38.p7	12:121401352	CAGAAGGCTATAGGT[A/T]TCaaaaaaaaaaaaa	80196
rs12369641	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421285	ctcacaactgtaatt[C/T]taggactttgggagg	80196
rs12371831	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401344	TTACAAGGCAGAAGG[C/T]TATAGGTATCaaaaa	80196
rs12810275	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399544	AGAGCCCTTGGTTTT[C/G]TAAGTGTTTTCAATA	80196
rs12811672	snp	G/T	0	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399520	TTTTCAAAGAGCCCT[G/T]GGGATTTGAGAGCCC	80196
rs12812023	snp	A/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408913	AAAAGTTACAGGCCA[A/T]TCTGTGGTAAAAAGG	80196
rs12813638	snp	G/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408914	AAAGTTACAGGCCAA[G/T]CTGTGGTAAAAAGGA	80196
rs12815395	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412786	ctggagtgcagtggc[A/G]tgatctcggctcact	80196
rs28398328	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424737	AAAAGAAAAAAAAGA[A/G]AAAAACAATGCCACA	80196
rs28493526	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424726	AAAAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAA	80196
rs28557279	snp	A/C	0.255521	0.249939	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423621	CCCAAACTTGACCCC[A/C]AACATTTCAATGCAC	80196
rs34194877	snp	A/G	0.0704125	0.17392	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403128	GAGGCCGGGCGCGGT[A/G]GCTCACGCCTGTAGT	80196
rs34621569	in-del	-/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398881	ATTATTTCAGTCTAA[-/G]GGAAGTGGCCTGCCA	80196
rs34735211	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422155	GTACTTTGCGGCGTA[A/G/T]GATATAACATGGTTG	80196
rs34812514	snp	C/G			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420664	ATGAGCGTGCGCCAG[C/G]TGAAGGAAATTCTGG	80196
rs34892758	in-del	-/G			intron-variant	RNF34	GRCh38.p7	12:121400617	ACTAACCCAAGTGTT[-/G]GGGGACATCGTGGGA	80196
rs35270866	in-del	-/AGT	0.492484	0.0608394	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419576	TGGTGCCTGGCAATC[-/AGT]AGGGTGGAATATTTG	80196
rs35375423	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416859	AGACCCATCATATTG[-/G]GTAGGCCTCCTTGCT	80196
rs35628523	in-del	-/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407799	GTGCAGAAGAGGGAT[-/C]CCTTGTTGGTTATGA	80196
rs35917782	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413575	GCCACCATGCCCAGC[-/T]TTTTTTTTTTTTTTT	80196
rs35925457	in-del	-/A/ACAA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421371	AGAGATCCCATCTCT[-/A/ACAA]AAAAAAAAAAAAAAA	80196
rs36077205	in-del	-/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424549	TAGCTTGGACAACAT[-/G]GGCGAAACCCTGTCT	80196
rs41367546	snp	A/C	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417432	ATTAAATTTTAGTAG[A/C]AGGCRGAAAGAAAAC	80196
rs41422244	snp	C/T	0.00161617	0.0283809	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402846	YGTTATTGTAATAAT[C/T]GATCAGTTTGGCCAA	80196
rs41468645	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417437	ATTTTAGTAGMAGGC[A/G]GAAAGAAAACTCATG	80196
rs41507449	snp	A/G	0.00902168	0.0665541	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417808	CTAGCTTTTTTACAC[A/G]TTCGTTTTTTTCAAA	80196
rs55639228	snp	A/C	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409467	CTCAGGAATTTGTGG[A/C]GGGTGATGTCCCAGC	80196
rs56174403	snp	C/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403600	TTGAGTTTTAGCAAA[C/T]TGAAGGTTGTCCAGA	80196
rs56196633	snp	C/T	0.333261	0.235728	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406745	ATTTTTAGTAATCAC[C/T]GATGACTAGAAAATA	80196
rs57206363	snp	G/T	0.3512	0.228601	intron-variant, utr-variant-3-prime	RNF34, KDM2B	GRCh38.p7	12:121402436	CTTTCTCCCTTTGGC[G/T]TTTTGGTTTGGTTTG	80196
rs57222350	snp	C/T	0.0107246	0.0724382	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418926	TGGTCAGGCTGGTCT[C/T]GAATACCTGACCTCA	80196
rs57636873	snp	C/T	0.3512	0.228601	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402001	CTTAATGTTGATTTA[C/T]ATTGAAATTGTTTAA	80196
rs57703781	snp	C/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410253	TTTTCAAATATGCTG[C/G]ATGGGGCTGGCGTGG	80196
rs57800170	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421370	AGAGAGATCCCATCT[C/T]TAAAAAAAAAAAAAA	80196
rs57913468	snp	A/C	0.0596104	0.162024	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399906	GGTCTTCGCTCGGGG[A/C]GGAAAAGAATCCTCC	80196
rs58583717	snp	C/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411503	TTTGAAAAATTGTAT[C/T]CTTCCCTAATTCATT	80196
rs58750993	in-del	-/C	0.5	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399644	GCCCCGAGGTCATCA[-/C]CGAGCATGAACGCGG	80196
rs59183074	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410163	CGTCTCAAAAAAAAA[-/A]GAAAAGGAATTATGT	80196
rs59199848	snp	A/G	0.390651	0.206682	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403345	AGTTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	80196
rs59253955	in-del	-/A	0.487871	0.076925	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410546	TGTCTCAAAACCACC[-/A]AAAAAAAAAAAATGC	80196
rs59558352	snp	C/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412388	GGGACTACAGGTGCC[C/T]GCCACCACGCCAGGC	80196
rs59645029	snp	A/G	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409918	CCCAGCACTTTGGGA[A/G]GCCGAGGCGGGCGGA	80196
rs59697780	snp	A/G	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407566	TACGCCTAGTATGCT[A/G]TCTTTCCAGGAATTG	80196
rs59746769	in-del	-/AATAAA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408464	AAAAATAAAAATAAA[-/AATAAA]TAAAAACTAGAAAAT	80196
rs59834647	snp	C/G	0.0726307	0.176182	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398244	GGGCGCGGTGGCGGG[C/G]GCCTGTAGTCCCAGC	80196
rs59966462	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419018	CAAGAGTGTCTTTTA[A/G]TTAGTAAATGAATAA	80196
rs60270456	snp	C/T	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409814	TTCACTGAAGGGCAG[C/T]GGGGGTGGGTGTTAC	80196
rs60582822	snp	A/G	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411756	AAGAAGTTTTTGTCC[A/G]TGAGGAACTTTCACT	80196
rs60801024	snp	A/G	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410687	ATGATAACTATAAGT[A/G]GATTTGCCCTTCAAT	80196
rs60900182	in-del	-/A	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403426	AAACAAAAAAAAAAA[-/A]GGATAAAGATTTTGC	80196
rs60970745	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421368	ATAGAGAGATCCCAT[C/T]TCTAAAAAAAAAAAA	80196
rs61079975	snp	C/T	0.0134861	0.0810011	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414821	CTGGGAGGCTGGGCA[C/T]GGTGGCTCATGCCTG	80196
rs61201057	snp	A/G	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418229	AAGTAGCACATACAC[A/G]TTTGTAGTGTTATGT	80196
rs61221047	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399777	CCTCCCCGGAAACTT[G/T]ACCACCTAGCCCAGA	80196
rs61659403	in-del	-/TTG	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405405	GTATATTATCCAGAC[-/TTG]TTGGCTACAGAGCTA	80196
rs61733229	snp	A/G	0.029116	0.117091	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400138	CCGCCCAGAGGGAAG[A/G]AGGTCGGCAGTGTGA	80196
rs61739898	snp	A/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420310	TGAGGATGATGATGA[A/T]GAAGAAGAAAACGCA	80196
rs61751317	snp	A/T	0.000446488	0.0149347	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420313	GGATGATGATGATGA[A/T]GAAGAAAACGCAGAG	80196
rs61754471	snp	A/G	1.67604e-05	0.00289481	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423512	CCAAGTGCGGCAAGC[A/G]CATGAGTGAGTGTCC	80196
rs61760895	snp	A/C	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416316	ACCCACCAGCAGCTA[A/C]GGAAGGGCCCAACAT	80196
rs61955092	snp	A/T	0.416218	0.186739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415083	CCTGGGCAACAAGAG[A/T]GAAGTTCCATCTCAA	80196
rs61955093	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423365	CTGAAGCCGAGGCCT[A/T]AGCTCTCTGTTGCCT	80196
rs67472562	in-del	-/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404412	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTC	80196
rs68064188	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413595	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	80196
rs71454696	snp	G/T	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404452	CAGGCTGGAGTGCGG[G/T]GGCACCATCTCAGCT	80196
rs73407605	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402729	TTCCTTTTCCTTTTT[C/T]TTTCTCTGAAAGGTG	80196
rs73407607	snp	C/G	0.00716266	0.059414	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403614	ACTGAAGGTTGTCCA[C/G]AGTTTGAAACAAACC	80196
rs74709796	snp	A/G	0.021333	0.101051	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414248	ACTAATACCTCAGCT[A/G]TCTCGACTTCCATTA	80196
rs75522792	snp	A/G	0.0310518	0.120672	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408814	TTCACACAAGAAAAC[A/G]TGCAGAGGAGTTAAG	80196
rs75616931	snp	A/G	0.185155	0.241444	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421197	TAGTTCTTAGCATCA[A/G]CTATCTGTAGATTTC	80196
rs75714012	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424710	AGCCAGACCTTGTCT[A/C]AAAAAAAAAAAAAAA	80196
rs75734449	snp	A/C	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403397	CAAGACTCTGTCTCC[A/C]AAAAAAAAAACCAAA	80196
rs75804679	snp	A/C	0.0733688	0.176922	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405506	TTTTTCTTTTTGAGA[A/C]AGGGTCTTGCTCTGT	80196
rs75955894	snp	C/T	0.390651	0.206682	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409477	TGTGGAGGGTGATGT[C/T]CCAGCTGAAACAGTG	80196
rs76518376	snp	A/C	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421373	GAGATCCCATCTCTA[A/C]AAAAAAAAAAAAAAA	80196
rs76542175	snp	C/T	0.00358779	0.0422022	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414340	TCGTTCTAAACACTA[C/T]AGCTTTTATTTTAAG	80196
rs76598395	in-del	-/G	0.00279162	0.0372561	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423074	CTTTTTCTAGTTACA[-/G]AAGTAATATATCCCT	80196
rs76652312	snp	C/T	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403734	CTGAGACAATTATTT[C/T]TGAATTTAAAACTTC	80196
rs77286564	snp	A/G	0.00676609	0.0577691	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423650	ACAGAAGGGACTGGA[A/G]AGTTATGTTCAAAGG	80196
rs77443157	snp	A/G	0.0314385	0.121371	intron-variant	RNF34	GRCh38.p7	12:121401157	AGATTTACTATAGAA[A/G]ATTGAAAAAGAGTGT	80196
rs77507303	in-del	-/T	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413021	ATTGTGCCCAGGCTA[-/T]TTTTTTTTTCCTTCC	80196
rs77552790	snp	G/T	0.0111196	0.0737302	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415878	CATGCCTGTGTACAT[G/T]TATCTGTTTTGGGTG	80196
rs77730756	snp	A/C	0.350764	0.228794	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399517	AGCTTTTCAAAGAGC[A/C]CTTGGGATTTGAGAG	80196
rs77821626	snp	A/C	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409567	TGTATATCAGAATTA[A/C]CCAGGGAGTTTTCAA	80196
rs77970809	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412850	CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGATTAC	80196
rs78030102	snp	G/T	0.5	0	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420796	AGGTTTATCTTTTCA[G/T]TTTTTCCCTGTAGTA	80196
rs78071836	snp	C/T	0.0314385	0.121371	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422074	GAGGGGAGAAGTCAG[C/T]TGACTTCATAAATGT	80196
rs78146460	snp	C/T	0.0115144	0.0749975	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421844	CTAGCTTAAACAGCC[C/T]TCCCATCATTAACTT	80196
rs78166997	snp	C/T	0.0310518	0.120672	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417092	AGATCAGTTGCCTTT[C/T]TCTTTCCCTGTCAGT	80196
rs78205157	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399863	AAAGCAGCGCCGCAG[C/G]GCGCCTTCCGCCACG	80196
rs78415178	snp	A/T	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410580	ATGGGAAAAAAAAAA[A/T]TACTTCAAATATACT	80196
rs78570062	snp	A/G	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402951	AGAGAAATAATTTAG[A/G]ATGTAGAATTCCTTC	80196
rs78573621	in-del	-/T	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413137	TTCAAGCGATTCTCC[-/T]GCCTCGGCCTTCCAA	80196
rs78719350	snp	A/C	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416797	TTAGAGATTCAACAT[A/C]AAATACTTAGCTAAC	80196
rs78901279	snp	A/G	0	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403411	CAAAAAAAAAAACCA[A/G]AACAAAAAAAAAAAA	80196
rs79012375	snp	A/G	0.350982	0.228698	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405588	TCCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCACC	80196
rs79084421	snp	A/C	0.0807149	0.183963	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414270	CTTCCATTACCTATC[A/C]CATTATCTAGATTCT	80196
rs79123623	snp	G/T	0.3512	0.228601	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420940	TATAGATCTGGAAAG[G/T]AGTAACTTCATTATG	80196
rs79172008	snp	C/G	0.184838	0.241358	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419610	TTGGGAACCGACCTA[C/G]CTTATTGGAGAGCTA	80196
rs79330682	snp	A/C	0.5	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398371	AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAATT	80196
rs79540358	in-del	-/GTTGTTGTTGTTGTT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406304	GTTGTTGTTGTTGTT[-/GTTGTTGTTGTTGTT]TGAGACAGACTCTTG	80196
rs79602836	snp	A/G	0.0165278	0.0893908	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418255	TATGTGTTAGTGCAC[A/G]TGTTTCAGTGACCAC	80196
rs79716797	snp	A/C	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412645	TGGCCTCCCAAAGTG[A/C]TGAGATTACAGATGT	80196
rs79807208	in-del	-/T	0.0737376	0.17729	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406453	CCTGACTAATTTTTT[-/T]GTATTTCAGTAGAGA	80196
rs111378433	snp	A/G	0.0475351	0.146656	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407309	GGTTTTTTTCCCCCA[A/G]TGAACAAATAATGGA	80196
rs111388380	snp	G/T	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404636	CCTCAAGTGATTCTG[G/T]CCTCCTAAAGTGCTG	80196
rs111466028	snp	A/G	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420236	AGATACGTTGTATAA[A/G]TGTAGGTACAAAGTG	80196
rs111571472	snp	A/C/T	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423622	CCAAACTTGACCCCC[A/C/T]ACATTTCAATGCACA	80196
rs111780423	snp	A/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410095	GGAGGTAGAGGTTGC[A/G]GTGAGCCAAGATCGT	80196
rs111951207	snp	C/T	0.5	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399797	CCTAGCCCAGAAAGC[C/T]GCAGCAGCTTCCTCA	80196
rs112083066	snp	C/G	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403212	CCATCCTGGCTAACA[C/G]AGTGAAACCCTGTCT	80196
rs112104048	snp	A/G	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418023	CAAGTCATGTGCTGG[A/G]GTGAAGCTTCCACAC	80196
rs112166347	snp	A/G	0.0325976	0.123435	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424434	GGTGGGAGCACCTTC[A/G]AAGATGTCACATGGG	80196
rs112382698	snp	C/T	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412230	CCATGCCCAACTAAT[C/T]TTTTTTTTTTTTTTT	80196
rs112419342	snp	C/T	0.00953873	0.0683987	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404342	CATAAACTTTCTTTT[C/T]CCACTCTCCCCCTAT	80196
rs112532382	snp	G/T	0.00755907	0.0610114	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418897	TTTTTAGTAAAGATG[G/T]GGTTTCACCATGTTG	80196
rs112607887	snp	A/G	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402873	CCAATGTCTTGTCTA[A/G]AAGTATTACATTTTA	80196
rs112773484	snp	A/G	0.000181185	0.00951628	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416261	TTTGCAGGAGCCACC[A/G]GTCCATTCAGATTTA	80196
rs112786606	snp	C/G	0.5	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400010	GCCTCCCGAAAGTCG[C/G]CTTCCTATTGGTCGT	80196
rs112812260	in-del	-/A	0.5	0	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424710	GCCAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA	80196
rs112921407	snp	C/T	0.5	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398264	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	80196
rs113095218	in-del	-/A	0.350546	0.22889	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410154	GCGAAACTCCGTCTC[-/A]AAAAAAAAAGAAAAG	80196
rs113326640	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398838	TATCTGAGCAGCACT[C/T]GAAGCAAGAGAAATA	80196
rs113356293	snp	C/T	0	0	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400060	TTTTACCGGGGCACG[C/T]GGCGAGCGTGACCAC	80196
rs113384828	snp	C/G			intron-variant	RNF34	GRCh38.p7	12:121400375	CTTCAGGTGCCCCAA[C/G]CGAGCCAGGGCAGGC	80196
rs113432721	snp	A/G	0.5	0	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420734	GGGAACTGGTAGAGA[A/G]AGTAAACCGGTTATA	80196
rs113535252	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405903	GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCT	80196
rs113569984	snp	A/G	0.3512	0.228601	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413112	CTCACTGCAACCTCC[A/G]CCTCCCCGGTTCAAG	80196
rs113603645	snp	A/G	0.5	0	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404644	GATTCTGGCCTCCTA[A/G]AGTGCTGGGATTAGA	80196
rs113741957	snp	A/G	0.5	0	intron-variant	RNF34	GRCh38.p7	12:121401771	AGACGTGTGTTTTGA[A/G]TTGAAGTGGAAGGTA	80196
rs113850313	snp	C/T	0.0325976	0.123435	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424452	GATGTCACATGGGGG[C/T]CGGGTGCGGTGGCTC	80196
rs114043273	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419792	TAGATTGTCTAAGTA[C/T]GCTGTGGTAGGACTG	80196
rs114179027	snp	G/T	0.0547245	0.156101	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399908	TCTTCGCTCGGGGCG[G/T]AAAAGAATCCTCCCC	80196
rs114285155	snp	A/G	0.0607341	0.163335	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422518	TCCACACCAGTAGTC[A/G]TGGGCCATGAACTAA	80196
rs115198333	snp	G/T	0.0547245	0.156101	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405109	CTCTTACGCAGATTA[G/T]TTAGGTTTGTATTCT	80196
rs115618932	snp	C/T	0.0310518	0.120672	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404249	TGAGCTCAGGCAGTC[C/T]ACTTGCCTTGGCCTC	80196
rs115944827	snp	G/T	0.0554779	0.157039	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421602	TTGGCACAGAAATTC[G/T]TCCTCAGCTGGTAAC	80196
rs117056373	snp	C/T	0.021333	0.101051	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399919	GGCGGAAAAGAATCC[C/T]CCCCGCGCACTCCCA	80196
rs117120114	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402159	GCAAGTATACCTGGC[C/T]GGGTGCAATAGCTCA	80196
rs117160881	snp	G/T	0.0252325	0.109451	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414102	ATTTTAAGGTTGAGG[G/T]CTTTTTATTTGCTTT	80196
rs117220933	snp	C/T	0.0205511	0.0992634	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402983	TTTGTGGTATATGGT[C/T]GGATATTTGGTCACT	80196
rs117736614	snp	A/G	0.0825414	0.185628	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409219	TCCTGTCCTCAGGTG[A/G]CCTGCTGGCCTCGGC	80196
rs118005823	snp	A/G	0.0158469	0.0875917	intron-variant	RNF34	GRCh38.p7	12:121400624	CCAAGTGTTGGGGAC[A/G]TCGTGGGACCGAGGA	80196
rs137857947	snp	A/C	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403960	TGGCATTATTATTAC[A/C]TTGCTATTTACCTAG	80196
rs138143734	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422365	TGGCTCCTCTGCTTT[A/C]CTAAGTTCTAAAGAG	80196
rs138199363	snp	A/G	2.14034e-05	0.00327128	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420247	ATAAGTGTAGGTACA[A/G]AGTGAAATCACTTCA	80196
rs138299103	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405210	GGGAACAGTATGGGA[A/G]AAACACTGTCAGTCT	80196
rs138379218	snp	A/T	0.00358779	0.0422022	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417246	TATACCAAGGGGTGG[A/T]AAGGTTTTAATTCAT	80196
rs138434056	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419989	ACCTTCCTGAGAGAG[-/T]TAATACTCTGGTTAG	80196
rs138681520	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417994	TTTAGTGCTTGATGA[C/T]TTCTGATAAACTTCA	80196
rs139024381	snp	A/G	0.00835141	0.0640778	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419336	TACACTGTGATGTTC[A/G]CACAATGACAAAATC	80196
rs139160366	snp	C/T	0.0429648	0.14013	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406443	AGGCACTTGCCACCA[C/T]GCCTGACTAATTTTT	80196
rs139170044	in-del	-/CCCCCC/GAAACCCCC			cds-indel, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423422	GGATGAGGAAGACGA[-/CCCCCC/GAAACCCCC]CAGCCTGTGTCGCAT	80196
rs139288912	snp	G/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420602	TCTCCAAGGAGAGAG[G/T]GAGAGCTTCACTGTC	80196
rs139296354	snp	C/T	0.0314385	0.121371	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413702	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	80196
rs139336092	snp	C/T	0.00914312	0.0669923	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418456	TAACATGTAAAGGCT[C/T]GTAATTAATATTTAC	80196
rs139422249	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412882	GGTGCCTGGGCCAGC[C/T]ATTTTTGTATTTTTA	80196
rs139546535	snp	C/T	0.0107246	0.0724382	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422544	ACTAAGACCCCAGAT[C/T]ACAAGAATCTCTCCC	80196
rs139787083	snp	A/G			intron-variant	RNF34	GRCh38.p7	12:121401247	AGGGAGACATGGTGA[A/G]GAGAAGTAATTCAAA	80196
rs139825196	snp	G/T	0.0115144	0.0749975	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407031	AGGTAGTGAACACAG[G/T]ACCCAACAGTTAGTT	80196
rs140143041	in-del	-/C	0.445196	0.1562	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415089	AACAAGAGTGAAGTT[-/C]CCATCTCAAGAAAAA	80196
rs140213777	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423844	AGTCAGCCTGTTTGC[A/G]CCATGTGGGCATCAG	80196
rs140252700	snp	A/G	0.0547245	0.156101	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403297	GCTACTCTGGAGGCT[A/G]AGGCAGGAGAATGGC	80196
rs140742825	snp	C/T	0.00795532	0.062565	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415367	GGCTCACACTTGTAA[C/T]CTGAGCACTTCAGGA	80196
rs140745383	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400520	TGTGCGCCTCCTCGG[C/G]GGCCTGAGGCAGAGC	80196
rs140798762	snp	A/C	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408962	ATCAGATTGTTAAAA[A/C]CTCAGGTGACCCTTT	80196
rs141042508	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424305	ATTTTCAGTGCTACC[C/T]GCTAGCTGATTTTAA	80196
rs141081411	snp	A/G	0.0310518	0.120672	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410445	GGGAGGCTGAAGCAG[A/G]AGAATTGCTTGAACC	80196
rs141105657	snp	A/G	8.24654e-05	0.00642074	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417540	AAGGATTTTTGCTCC[A/G]TTTGTTCAGTCTTAC	80196
rs141404014	snp	C/T	0.00557542	0.0525036	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421619	CCTCAGCTGGTAACA[C/T]GATCAAGCCACGGAA	80196
rs141526270	in-del	-/TC	0.0185938	0.0946107	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418279	GACCACAGAAAACAA[-/TC]TCAGTAGTGTAAGTT	80196
rs141745301	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416634	TTTTATTTTCTATTA[C/T]GTTTATTTCCAAAAG	80196
rs141786813	snp	A/G	0.00438332	0.0466095	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419649	TATAGTCAAAAGAAA[A/G]TATGTGAAGGAAGGT	80196
rs141914430	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399855	CAACCGAGAAAGCAG[C/T]GCCGCAGCGCGCCTT	80196
rs142087959	snp	A/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419121	ATAGACCACATACAC[A/G]GCAGTGGTTCTGTAA	80196
rs142217962	snp	C/T	0.0107246	0.0724382	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398658	AACCATGGCTTTGTA[C/T]CCCAAGAACATTTTT	80196
rs142305118	in-del	-/A	0.0310518	0.120672	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411279	TAAGTGTTTTTCTTC[-/A]TTTTCTTTCTGGGGA	80196
rs142546121	snp	C/G	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418502	TCTAAACTGCTGAAA[C/G]AAATGTTTTGAACAA	80196
rs142639830	snp	A/G	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422407	CCTCCACACAGAAGG[A/G]GAGACCAAGGCCCAC	80196
rs142733577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407111	TGTTCTTTCTAAACT[A/G]TTAGAAAAAGGGTTA	80196
rs142943995	in-del	-/A			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398372	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAATTT	80196
rs143025348	in-del	-/AT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418014	GATAAACTTCAAGTC[-/AT]GTGCTGGAGTGAAGC	80196
rs143077452	snp	A/G	0.00398564	0.0444627	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406507	GCCCACGCTGGTCTC[A/G]AACTCCTGAGCTCAA	80196
rs143103429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403032	TGCATATTGTATTTC[A/G]GTTGAAGCAGCAGTT	80196
rs143117593	snp	C/T	0.0607341	0.163335	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412270	TTTGAGATGGAGTCC[C/T]GCTCTGTTGCCCAGG	80196
rs143210041	snp	A/G	1.64732e-05	0.0028699	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417696	GATACTTGTCGTGAG[A/G]AAGAAGACTTGGTGG	80196
rs143217753	snp	G/T	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420744	AGAGAAAGTAAACCG[G/T]TTATACAAAGAGAAT	80196
rs143285387	snp	A/G/T	6.59287e-05	0.00574113	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420583	TGGTTTCAGAACCCC[A/G/T]GGCTCTCCAAGGAGA	80196
rs143648835	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412260	TTTTTTTTTTTTTGA[A/G]ATGGAGTCCCGCTCT	80196
rs143834959	snp	A/G	0.0123036	0.0774623	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409582	CCCAGGGAGTTTTCA[A/G]AAAAATTCTGGTGCC	80196
rs144021288	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408305	AAATTACCAGGGTGT[A/G]ATGGCAGGCACTTGT	80196
rs144069576	snp	G/T	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413872	GAGCCACCGCGCCCG[G/T]CTTCACCTGACTTTT	80196
rs144086612	snp	C/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416329	TACGGAAGGGCCCAA[C/G]ATAGTTTGTAAAGCC	80196
rs144288733	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404191	TCTTCGTATTTAGTA[A/C/G]AGACGGAGTTTCACA	80196
rs144296164	in-del	-/AA			intron-variant	RNF34	GRCh38.p7	12:121401162	TACTATAGAAGATTG[-/AA]AAAGAGTGTCAGCTG	80196
rs144358195	in-del	-/GTTGTTGTTGTTGTT	0.416545	0.186448	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406283	TTATGGAATGTGTAA[-/GTTGTTGTTGTTGTT]GTTGTTGTTGTTGTT	80196
rs144493337	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423040	CAAAGCCCATCTACA[G/T]AAGACCAGCTGAGGG	80196
rs144605495	snp	A/G	0.0130921	0.0798413	intron-variant	RNF34	GRCh38.p7	12:121400725	ATGCCACCCGGAAGG[A/G]GTGCTTCGTAGGCTG	80196
rs144703856	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414501	CCTGGTGGCTCAAAG[A/G]GAGGGAAGAGACAAG	80196
rs144788428	snp	A/T	0.0310518	0.120672	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399306	CAGTGAGCCGAGATC[A/T]CACTATTGCACTCCA	80196
rs144819272	snp	A/G	0.00257381	0.035781	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423457	ATGGATGCCGTCATC[A/G]ACTGTGTCCTACTGG	80196
rs144970416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419386	AGAACGTCTCCTAGT[C/T]GTCAAGCAACACATA	80196
rs145004602	snp	A/G	0.0263992	0.111815	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402254	AACAGCTTGGCCAAC[A/G]TAGCAAAACCCTGTC	80196
rs145010576	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423147	ACATAGCTAACATTT[A/G]TTGGGTACGTCAAGC	80196
rs145447461	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415450	ACATGGTGAAACCCA[A/G]TCTCTACTAAAAATA	80196
rs145495936	snp	A/G	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416207	GGGCTGCTGAATGAA[A/G]TCATGGGAACTGGAG	80196
rs145599445	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422029	TTCAGAGGTCGTAGG[C/T]TGCTGGCTGGGAAAT	80196
rs145652750	in-del	-/T	0.00780721	0.0619891	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417484	ATCTTGCTGTCATCA[-/T]AATGCTTTTCTTTCT	80196
rs146001775	snp	C/T	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422454	GTTGCCTAGTGCCTT[C/T]TCCATTGGCATATCT	80196
rs146436628	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408617	ATTTCTGAAATTTAT[A/G]AGAAAGTACAGGAAG	80196
rs146497196	snp	A/G/T	0.000164724	0.00907396	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416350	TTGTAAAGCCTGTGG[A/G/T]CTTTCATTTTCAGTC	80196
rs146717385	snp	A/G	0.00398564	0.0444627	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408119	GAGATCAGCCTGGGC[A/G]GCATATCAAGACCCC	80196
rs146824763	in-del	-/AAAAAAA			intron-variant	RNF34	GRCh38.p7	12:121401353	GAAGGCTATAGGTAT[-/AAAAAAA]CAAAAAAAAAAAAAA	80196
rs147032853	in-del	-/AGT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419577	GGTGCCTGGCAATCA[-/AGT]GGGTGGAATATTTGA	80196
rs147069367	snp	A/C	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417234	TAATTACATGTTTAT[A/C]CCAAGGGGTGGAAAG	80196
rs147092139	snp	A/G	0.000473391	0.0153776	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420227	GACCTAATCAGATAC[A/G]TTGTATAAGTGTAGG	80196
rs147553178	snp	A/G/T	3.72682e-05	0.00431656	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423595	AGGCTCCCCTCACCA[A/G/T]GACAGTCACCCCCAA	80196
rs147866946	snp	C/T	0.00159617	0.0282053	intron-variant	RNF34	GRCh38.p7	12:121400786	GATGTGCCTCCATCG[C/T]CACTAGGTAAACGCA	80196
rs147940397	snp	C/T	0.00795532	0.062565	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415896	TCTGTTTTGGGTGGG[C/T]AGGGAGGTTTTTTGT	80196
rs147950606	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419547	GGGTGATGTGGATTG[C/T]TGGATGCTACAGTAT	80196
rs148275322	snp	C/G/T	4.94192e-05	0.00497067	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417740	CCATCATGGACTAGG[C/G/T]TCTGAGGACGACATG	80196
rs148311487	snp	A/G	0.0228947	0.104514	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421488	AGCCTGCAGGGAGCC[A/G]TGGTCATGCCACTGC	80196
rs148409841	snp	C/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423096	TATATCCCTATCACA[C/G]ATGTCTTGAATTAGA	80196
rs148549696	snp	A/T	0.0023933	0.0345097	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399475	CAAATTCTTTTATTA[A/T]GCTACGATTTTGGTT	80196
rs148644546	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419037	GTAAATGAATAAATG[C/T]AGAGGGAAATTTGGT	80196
rs148694694	snp	A/G	0.0607341	0.163335	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413224	TAGAGACGGCGTTTC[A/G]CCATGTTGTCCAGGC	80196
rs149083024	snp	A/G	0.00914312	0.0669923	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402927	CCTGCTTAATGTCCA[A/G]ATGGTATGAGAGAAA	80196
rs149335072	snp	A/G	0.00755907	0.0610114	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418115	GCTCCAAAGTCTGCT[A/G]TCTGAAGGGTCCCAA	80196
rs149598276	in-del	-/CC			intron-variant	RNF34	GRCh38.p7	12:121400227	CATGAAGGTGAGGGG[-/CC]GGTGGAGCCGGACAG	80196
rs149671327	snp	C/T	0.00993419	0.0697739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415412	GATCACTTGAGGCCA[C/T]GCATCTGAGACCAGC	80196
rs149715112	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407822	GGTTATGACCCTACC[A/G]GATATGGTAACTGGG	80196
rs150250138	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410971	ACAGGGTCTCACTCC[A/G]TCACCCAGGCTGGAG	80196
rs150408238	snp	C/T	1.65894e-05	0.00288	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417894	GACCAAACATCCAGA[C/T]CTGGAGTGCCGGCAC	80196
rs150480808	snp	C/T	0.0103295	0.0711199	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404590	GAGACCGGGTTTCAC[C/T]ATCTTGGCTAGGCTG	80196
rs150552544	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412358	CATTCTCCCACCTTA[A/G]CCTCCCGAGTAGCTG	80196
rs150587957	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407398	AAATTCAGAAGCCAA[A/G]AGGGTATGCCTAGTA	80196
rs151100805	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424042	CTTTATTAGTCATGT[A/G]TATTTTAAATGCTAA	80196
rs151144914	snp	C/T	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419252	CACTAACGTGATGTA[C/T]GGCTTCGTAGCCGGC	80196
rs151187360	in-del	-/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412230	CCATGCCCAACTAAT[-/C]TTTTTTTTTTTTTTT	80196
rs180874457	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418584	AGGAAAGCTGGATGC[A/G]GTGGTGTGAGCCTGC	80196
rs180884285	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403703	GCTCCTTGGTCCTTG[C/T]AGATTCATGTAGCAT	80196
rs181069525	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399501	TGGTTATTTTGAATA[A/C]AGCTTTTCAAAGAGC	80196
rs181081695	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421414	CCAAAAAAACCTGGT[A/G]TGGTGGCACCAGCCT	80196
rs181595445	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418432	AGGTCCTTGGACATC[A/C]TGATTGAATAACATG	80196
rs181602120	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411433	TTACCAGAGCTGTGT[A/G]GTTGAAAAAAAAATT	80196
rs181816892	snp	C/G	1.64735e-05	0.00286993	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417717	GACTTGGTGGATCTA[C/G]TACTGTGCCATCATG	80196
rs181975056	snp	C/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404761	TGATAATATATTTAA[C/T]GGAATCATTAAAAGT	80196
rs182001879	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421787	TGGGCCACCATGCCT[C/G]ACCCTCAGTGGTGTT	80196
rs182007925	snp	A/C	0.0142736	0.0832652	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398975	AATGTATATAAATAA[A/C]AGAACAGTCTTAGGT	80196
rs182031296	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400143	CAGAGGGAAGGAGGT[C/G]GGCAGTGTGAGGAGC	80196
rs182375659	snp	C/T	0.000445857	0.0149241	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402827	CATTTGTATCTATAG[C/T]ACATGTTATTGTAAT	80196
rs182581069	snp	A/G	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410869	GTTAATATGTGTCTG[A/G]GTTGTACTGAATATT	80196
rs182812926	snp	A/G	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405673	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	80196
rs182932415	snp	C/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407756	AGGAAAGAACATGAA[C/G]TTAGGTCTCTAAAGC	80196
rs182966689	snp	C/T	0.0244538	0.107838	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414797	CGTGCCTTTGGCCCT[C/T]GCTGAAAGCTGGGAG	80196
rs183191791	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418782	CTAGAGTGAAGTGGC[A/G]AGATCTTAGTTCACT	80196
rs183199831	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398233	AAAAACTAGCCGGGC[A/G]CGGTGGCGGGCGCCT	80196
rs183486512	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419100	CTAATAATGTTTTGG[C/T]CAGTGATAGACCACA	80196
rs183521191	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423826	CCCGTGAACACTCAT[G/T]GAAGTCAGCCTGTTT	80196
rs183599162	snp	A/G	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416645	ATTATGTTTATTTCC[A/G]AAAGCAAGAAATTTG	80196
rs183699148	snp	C/G	0.00119737	0.0244387	intron-variant	RNF34	GRCh38.p7	12:121400912	GTTTCCGGCCTACTT[C/G]TGAGAGATGATTCTC	80196
rs183786304	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408813	TTTCACACAAGAAAA[C/T]GTGCAGAGGAGTTAA	80196
rs183849858	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419410	ACACATACTGTAGTC[A/G]TAAATTAGATAAGTC	80196
rs183880893	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398359	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	80196
rs183982568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403342	CAGAGTTTGCAGTGA[A/G]CCAAGATTGCGCCAC	80196
rs184201950	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409680	AAGACTTGCCTGGTG[A/T]GTCCAACATGCAGCC	80196
rs184217302	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413864	ACAGGTGTGAGCCAC[C/T]GCGCCCGGCTTCACC	80196
rs184548290	snp	C/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410403	TTAGCCGGGTGTGGT[C/G]GTGGGTGCCTGTAAT	80196
rs184665845	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417924	CAGGTACGAGGGGGT[A/G]ACTAATTACACCCAG	80196
rs184732914	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415897	CTGTTTTGGGTGGGT[A/G]GGGAGGTTTTTTGTT	80196
rs184892121	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398479	CAAATTCTCCACATC[C/T]TCACCATCTATTTTC	80196
rs184904177	snp	A/C/T	6.96064e-05	0.00589901	synonymous-codon, missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420332	GAAAACGCAGAGGAT[A/C/T]GGGTGAGGCCACCTA	80196
rs184979349	snp	C/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418599	GGTGGTGTGAGCCTG[C/T]AGTCTGATACTTGGC	80196
rs184984405	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399089	AATCGGCTGGGCCCG[G/T]TGGCTAATCTCAGCA	80196
rs185096803	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421191	GTTACATAGTTCTTA[A/G]CATCAACTATCTGTA	80196
rs185211970	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399622	TTACCGGACCCACGA[A/G]TGAGGAGCCCCGAGG	80196
rs185216751	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421457	ACTTGGGAGGCTGAG[C/G]GGGGAGGATTGCTTG	80196
rs185345399	snp	A/G	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403123	ATAAAGAGGCCGGGC[A/G]CGGTGGCTCACGCCT	80196
rs185506667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411017	ATAGCTCACCATAGT[C/T]TCAACCTCCCAGGCT	80196
rs185731627	snp	C/T	0.0123036	0.0774623	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405973	TAATTTTTTGTATTT[C/T]TAGTAGAGACGGGGT	80196
rs185775166	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404074	GGCTGGAGTGCAGTG[A/G]CACGATCTCAGCTCA	80196
rs185979955	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412165	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	80196
rs186280175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422808	GCCAAGAGCCAGGAC[A/G]GCCCATCTCTTTCAA	80196
rs186317006	snp	G/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418453	GAATAACATGTAAAG[G/T]CTTGTAATTAATATT	80196
rs186646962	snp	G/T	0.00159617	0.0282053	intron-variant	RNF34	GRCh38.p7	12:121400920	CCTACTTCTGAGAGA[G/T]GATTCTCAACCCGAT	80196
rs186729070	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419704	GTGTTTTCTAAAGTG[C/T]TCTGATTGAGAAATT	80196
rs186833228	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424749	AGAAAAAAACAATGC[C/T]ACATGAGCAACAGTG	80196
rs186959684	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401411	CCAGAAAGGATACTT[C/T]TGGCTACAGAAAGCA	80196
rs187073342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405075	TTATAACCTTATTGG[C/T]TGGAAACTGTCATTC	80196
rs187266213	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414854	ATCCCAGCACTTCGG[A/G]AGGCCGAGGTGGGTG	80196
rs187357001	snp	G/T	0.00517822	0.0506191	intron-variant	RNF34	GRCh38.p7	12:121400475	GTCCCTAGCGTTCGC[G/T]CCGGGTGGGCCCCTC	80196
rs187480409	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418888	ATTTTTGTATTTTTA[A/G]TAAAGATGGGGTTTC	80196
rs187484706	snp	C/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408419	CGCACTCCAGCCTGG[C/G]TAACAAGAGTGAAAC	80196
rs187530348	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409190	TTACCATGTTGGCCA[G/T]GCTGGTCTCAAACTC	80196
rs187798086	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414337	TATTCGTTCTAAACA[C/T]TATAGCTTTTATTTT	80196
rs187985452	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419199	TTTAGATACACAAAT[A/G]CTTATTACTGTGTTA	80196
rs188015976	snp	C/T	1.64999e-05	0.00287222	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416398	TTGGATGAAATGTTA[C/T]ATAACAACACACATG	80196
rs188072787	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399859	CGAGAAAGCAGCGCC[A/G]CAGCGCGCCTTCCGC	80196
rs188076750	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421478	GGATTGCTTGAGCCT[A/G]CAGGGAGCCGTGGTC	80196
rs188311504	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398290	GGCAGGAGAATGGCG[C/T]GAACCCAGGAGACGG	80196
rs188318418	snp	C/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403360	AAGATTGCGCCACTG[C/T]ACTCCAGCCTGGGCA	80196
rs188565453	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409860	TAAAATGAATGTAAA[G/T]AAATTATGTTCATGG	80196
rs189063926	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402978	CTTCCTTTGTGGTAT[A/T]TGGTCGGATATTTGG	80196
rs189121012	snp	A/G	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410494	GTGAGCCGAGATTGC[A/G]CCACTGCATTCCATC	80196
rs189301389	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411085	AGCACAGGCACATGC[C/T]ACCACACCTGGCTAA	80196
rs189546046	snp	C/G/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416988	CCTCTTTAAGCTTCT[C/G/T]TAGTGGCAAGGCTTT	80196
rs189677321	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421200	TTCTTAGCATCAACT[A/C]TCTGTAGATTTCTGT	80196
rs189899657	snp	C/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418175	AATTTCTCTGTCTTA[C/T]ACAGTTAGACACTAA	80196
rs189926709	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399105	TGGCTAATCTCAGCA[C/G]TTTGGAAGGCCGAGG	80196
rs189929462	snp	A/C	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403245	ACTAAAAATACAAAA[A/C]ATTAGCTGGATGTGG	80196
rs190055090	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406569	TAGGATTACAGGCGT[A/G]AGCCACCGCGCCGGG	80196
rs190300694	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413223	GTAGAGACGGCGTTT[C/T]GCCATGTTGTCCAGG	80196
rs190315684	snp	C/G	0.00835141	0.0640778	intron-variant	RNF34	GRCh38.p7	12:121400932	AGATGATTCTCAACC[C/G]GATCACTGAGAGTTC	80196
rs190400029	snp	A/G	3.29837e-05	0.00406088	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420567	GCTAATGGATGCTCT[A/G]TGGTTTCAGAACCCC	80196
rs190612857	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405258	AGAGGGACTTGAATA[C/T]TGAGGAGTTTCAGTG	80196
rs190717761	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414457	CAGTAAAAAGGAGAC[A/G]GGTTACTCTGGGCAG	80196
rs190734520	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404421	TTTTTTTGAGATGGA[A/G]TCTCTCTTTGTTGCC	80196
rs190770382	snp	A/G	0.00676609	0.0577691	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413671	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	80196
rs190921881	snp	C/T	0.000172048	0.00927331	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420283	CACAGAAGATGATGA[C/T]GACGACGATGATGAG	80196
rs190962060	snp	G/T	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418709	GTACCCCCAGCCTGG[G/T]CAACATAGCAAGACT	80196
rs191269243	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418454	AATAACATGTAAAGG[C/T]TTGTAATTAATATTT	80196
rs191315620	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424793	CTTGCTTATCAGTAA[A/G]GTTAACTGCTGATGT	80196
rs191383778	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401455	GAATAGGTAACTTTG[A/G]AACTGTGCCTTGAAG	80196
rs191630627	snp	A/G	0.0275645	0.114116	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398357	AGCCTGGGCGACAGA[A/G]CGAGACTCCGTCTCA	80196
rs191800360	snp	A/G	0.0130921	0.0798413	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403321	GAATGGCGTGAACCC[A/G]GGAGGCAGAGTTTGC	80196
rs191830083	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398189	CCATCCTGGCTAACA[C/T]GGTGAAACCCGTCTC	80196
rs191831301	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121400640	TCGTGGGACCGAGGA[C/G]AACAGGAGGGGTGCA	80196
rs192062634	snp	C/T	0.00993419	0.0697739	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409331	AACCAAAGTGGGATG[C/T]AAAATACTACATATC	80196
rs192094523	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423050	CTACAGAAGACCAGC[C/T]GAGGGTTTCTTTTTC	80196
rs192352613	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416515	AGCCATTTTCCATCT[A/G]GAAAAATACTTAATT	80196
rs192604672	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419827	CTTTCAAATCAGATG[C/T]CCCTGATGCTTGGGC	80196
rs192617912	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410218	AAATATGGGGCTTAA[A/G]GGGGAGATGGAAATT	80196
rs192853497	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419396	CTAGTCGTCAAGCAA[C/T]ACATACTGTAGTCGT	80196
rs192923920	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420929	ATGAGCCTGTTTATA[A/G]ATCTGGAAAGGAGTA	80196
rs192985562	snp	A/T	0.00516221	0.0505416	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415248	GTTTTCCAAGTCATT[A/T]AAAAAATTATTTACA	80196
rs193045780	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403086	CTAAGGAGCATATGT[G/T]TCTCAAATGGCTCTA	80196
rs193286748	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408434	GTAACAAGAGTGAAA[C/T]TCTGTCTAAAAAATA	80196
rs199515654	snp	A/G	0.000181703	0.00952986	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400203	CGGCCGAGCTGAGGC[A/G]GTCGCGGCCATGAAG	80196
rs199695141	in-del	-/GCCT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413527	GCGATTCTCCTGCCT[-/GCCT]CAGCCTCCCGAGTAG	80196
rs199742513	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415840	AGACTTTTGTCCAGT[C/T]TTTTTTTTTTTTTTT	80196
rs200116682	snp	A/G	1.6486e-05	0.00287102	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417549	TGCTCCGTTTGTTCA[A/G]TCTTACAAGAAAATC	80196
rs200273600	snp	C/T	3.51624e-05	0.00419284	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423572	TGCACGTGTTCAAGT[C/T]CTGAAACAGGCTCCC	80196
rs200332742	snp	G/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417825	TCGTTTTTTTCAAAC[G/T]ATACAGCCCCCTCTG	80196
rs200478156	in-del	-/TTGGGA	0.030665	0.119967	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421443	TGTGGTCCCAGCTAC[-/TTGGGA]TTGGGAGGCTGAGGG	80196
rs200480167	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406318	TTTGAGACAGACTCT[A/T]GCTGTGTCGCCCAGG	80196
rs200513045	snp	C/T	0.000166503	0.00912271	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423390	TTGCCTTTCAGATGG[C/T]GAGCGGCTGCAGCTG	80196
rs200788702	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416290	TACACCAAACCCTGA[A/G]TTTTCCACCTACCCA	80196
rs201019913	snp	A/G	6.59055e-05	0.00574007	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420695	CTCGGAATTTTGTCA[A/G]CTATTCTGGCTGTTG	80196
rs201069572	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413020	CATTGTGCCCAGGCT[-/A]TTTTTTTTTTCCTTC	80196
rs201157520	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422915	TCCTAACTTTCCTAA[-/G]GGGGGAACTAAGGCT	80196
rs201172818	snp	C/T	0.000462008	0.0151918	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402836	CTATAGCACATGTTA[C/T]TGTAATAATCGATCA	80196
rs201204148	snp	C/G	0.000399281	0.0141238	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417770	GGACACAAGCAGTCT[C/G]AATTCTTCAAGGTCC	80196
rs201268373	in-del	-/A	0.386884	0.209196	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402557	GATTAAAAAAAAAAA[-/A]TCCAAATTGGTGCCC	80196
rs201362422	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403612	AAACTGAAGGTTGTC[A/C]AGAGTTTGAAACAAA	80196
rs201432830	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414167	ATTTTACATGCTATT[-/A]TAAAATGTTTGACAG	80196
rs201536085	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416124	AGCCCAGATTCCACT[C/T]AGCTTTAAACTGTGG	80196
rs201673963	snp	A/C/T	9.9148e-05	0.00704026	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420542	GAGGGTCTGGACTTA[A/C/T]GGGACCAGGGCTAAT	80196
rs201929209	snp	A/G	4.94181e-05	0.00497057	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416185	GTCTATGTGGGCTTC[A/G]TGCTGTGGGCTGCTG	80196
rs201968366	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418176	ATTTCTCTGTCTTAC[A/T]CAGTTAGACACTAAC	80196
rs202010836	snp	A/G	1.64732e-05	0.0028699	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417680	GAGAAATATACCCAT[A/G]GATACTTGTCGTGAG	80196
rs202069016	snp	A/C	0.00199792	0.0315431	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402764	AGTGGTACTAAGGAT[A/C]AAGTATACTGTTAAA	80196
rs202132357	snp	C/T	8.86171e-05	0.00665588	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420286	AGAAGATGATGATGA[C/T]GACGATGATGAGGAT	80196
rs367629594	snp	A/C/T	4.9498e-05	0.00497459	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417539	GAAGGATTTTTGCTC[A/C/T]GTTTGTTCAGTCTTA	80196
rs367644293	in-del	-/A	0.361684	0.223667	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403415	AAAAAAAACCAAAAC[-/A]AAAAAAAAAAAGGAT	80196
rs367731648	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422917	CCTAACTTTCCTAAG[A/G]GGGAACTAAGGCTCC	80196
rs368005152	snp	G/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420323	GATGAAGAAGAAAAC[G/T]CAGAGGATCGGGTGA	80196
rs368018624	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403224	ACACAGTGAAACCCT[C/G]TCTCTACTAAAAATA	80196
rs368030223	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403135	GGCGCGGTGGCTCAC[A/G]CCTGTAGTCCCAGCA	80196
rs368081105	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406575	TACAGGCGTGAGCCA[C/T]CGCGCCGGGCTGGTG	80196
rs368172717	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422915	TTCCTAACTTTCCTA[A/G]GGGGGAACTAAGGCT	80196
rs368256317	snp	A/T	0.000153988	0.00877328	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400164	TGTGAGGAGCTGCTA[A/T]GGTGCTGAGTTTCCT	80196
rs368392505	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407196	CAACTAAGGTCCCCA[A/G]GTAGGTCATGAAAGC	80196
rs368427013	snp	C/T	4.95421e-05	0.00497681	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417853	CTGCTACTATGTCTT[C/T]GTTTCAGGGAGAGCT	80196
rs368457083	snp	C/T	0.00438332	0.0466095	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404215	TTTCACAATGTTGCC[C/T]AGGCTGGTCCCAAAC	80196
rs368558209	snp	A/C	0.00279162	0.0372561	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407777	TCTCTAAAGCTTTTA[A/C]AAGGAGGGTGCAGAA	80196
rs368630147	snp	A/G	4.95127e-05	0.00497533	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402847	GTTATTGTAATAATC[A/G]ATCAGTTTGGCCAAT	80196
rs368767001	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34	GRCh38.p7	12:121401008	TGCCGAACTCAAACC[A/G]AGTGGGATGAGTCAT	80196
rs368822975	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417473	ATAATGGTTTATATC[G/T]TGCTGTCATCAAATG	80196
rs368849518	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418930	CAGGCTGGTCTCGAA[C/T]ACCTGACCTCAGGTT	80196
rs369125307	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413932	GGGTGTGAAGACTTA[C/T]AATATTGAAATCCTT	80196
rs369150251	snp	A/G			intron-variant	RNF34	GRCh38.p7	12:121401694	ATTAAGGAACTAGCT[A/G]TCGAAGGAAAGAATT	80196
rs369386826	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424735	AAAAAAGAAAAAAAA[A/G]AAAAAAACAATGCCA	80196
rs369500317	snp	A/G	1.64876e-05	0.00287116	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416386	AAAGAAGGTGAGTTG[A/G]ATGAAATGTTACATA	80196
rs369581058	snp	A/G	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405561	CAATCTCTGCTTACC[A/G]CAACCTCCGTCTCCC	80196
rs369707785	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406084	ATGAGCCACCGTGCC[C/T]GGCCTGTCTTATTTC	80196
rs369744462	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415578	CCGAGATTGCGCCAC[C/T]GTACTCCAGCCTGGT	80196
rs369744966	snp	A/G	0.000177289	0.00941346	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423395	TTTCAGATGGCGAGC[A/G]GCTGCAGCTGCAGGA	80196
rs369753490	snp	G/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398166	ATCACGAGGTCAGGA[G/T]ATCGAGACCATCCTG	80196
rs369952588	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412682	TTGTGCCTGGCTGAA[C/T]ACTAACTTTAAATTA	80196
rs370193799	snp	A/G	0.000153988	0.00877328	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402823	GTAACATTTGTATCT[A/G]TAGCACATGTTATTG	80196
rs370203859	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403071	AAATCCTTTCACATT[A/C]TAAGGAGCATATGTT	80196
rs370330071	snp	A/G	0.000206686	0.0101637	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423562	GTGCGAGCCGTGCAC[A/G]TGTTCAAGTCCTGAA	80196
rs370393586	snp	A/G	0.000181185	0.00951628	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416312	ACCTACCCACCAGCA[A/G]CTACGGAAGGGCCCA	80196
rs370473629	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403144	GCTCACGCCTGTAGT[C/G]CCAGCACTTTGGGAG	80196
rs370507061	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410230	TAAAGGGGAGATGGA[A/T]ATTAAAATTTTCAAA	80196
rs370548063	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399790	TTGACCACCTAGCCC[A/G]GAAAGCCGCAGCAGC	80196
rs370594485	snp	G/T	0.000155988	0.00883004	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420374	TTCCCTGACATGTCA[G/T]CCTGACAGGAAGGGA	80196
rs370713779	in-del	-/A			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399360	CAAAAATAAAAAAAA[-/A]GGTGTAGGAAAATAA	80196
rs370728950	snp	C/T	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405807	ATTTCTTTTTTTTTT[C/T]TCTTGAGACGGAGTC	80196
rs370742713	snp	C/T	0.000153988	0.00877328	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417944	ATTACACCCAGGGCC[C/T]GGCACGCTTATTCTT	80196
rs370848382	snp	C/T	1.675e-05	0.00289391	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423535	GAGTGTCCCATCTGC[C/T]GGCAGTATGTGGTGC	80196
rs370917565	in-del	-/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398385	TCAAAAAAAAAAAAA[-/T]TTTTTTTTTTAAGAA	80196
rs371007642	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412534	AGGGGTGAGCCACCA[C/T]GCCTGGCCTAATTTT	80196
rs371429893	snp	C/G	0	0	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400158	CGGCAGTGTGAGGAG[C/G]TGCTATGGTGCTGAG	80196
rs371610614	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411794	AGGAGGCAACATCAG[A/T]CATGAATTAGAAGGG	80196
rs371636385	snp	G/T	1.64738e-05	0.00286995	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417636	TTAATGCGACTGAAG[G/T]TGAAGGACCTGCGGC	80196
rs371660693	snp	A/G	1.65067e-05	0.00287282	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420555	TATGGGACCAGGGCT[A/G]ATGGATGCTCTGTGG	80196
rs371667128	snp	A/G	0.0154538	0.0865337	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424604	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTAGG	80196
rs371779349	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422916	TCCTAACTTTCCTAA[A/G]GGGGAACTAAGGCTC	80196
rs371889967	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398099	CATTTTTGGGCCGGG[C/T]GCGGTGGCTCACGCC	80196
rs371944541	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409232	TGACCTGCTGGCCTC[C/G]GCCTCCCAAACTGCT	80196
rs372006434	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416420	ACACACATGGGTCAG[C/T]ATTCTTGATTGTAGG	80196
rs372156640	in-del	-/T	0.384976	0.210431	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404163	GCCATGCCCGGCTAA[-/T]TTTTTTTTTTTTTCT	80196
rs372267828	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423631	ACCCCCAACATTTCA[A/G]TGCACAGAAGGGACT	80196
rs372273481	snp	A/G	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408032	AAATGTGGGCCAAGC[A/G]TGGTAGCTCATGCCT	80196
rs372445215	snp	C/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121400011	CCTCCCGAAAGTCGG[C/T]TTCCTATTGGTCGTC	80196
rs372493833	snp	C/T	4.3123e-05	0.00464323	intron-variant	RNF34	GRCh38.p7	12:121400258	GACCCTCCTCGCCAA[C/T]CCTATCCTGCCAGGG	80196
rs372732361	in-del	-/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401966	TTGAGGATTTGGGCT[-/G]TTAAATGTTTATTAT	80196
rs372744345	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34	GRCh38.p7	12:121400681	AGGCTAGGGCCAGGC[C/T]AACGGGTTAAAGAAC	80196
rs372804221	snp	G/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404991	ACCTTTCCTCTTGCT[G/T]TTGTTGACTGTAATG	80196
rs372856839	snp	C/T	3.39127e-05	0.00411767	stop-gained, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423550	CGGCAGTATGTGGTG[C/T]GAGCCGTGCACGTGT	80196
rs372895681	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403521	TTAAACTGTAAAACC[A/G]ATTATTTTATATCAC	80196
rs373171102	snp	C/T	1.92509e-05	0.00310243	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423450	CATCTGCATGGATGC[C/T]GTCATCGACTGTGTC	80196
rs373182097	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406195	AGAGGAGAACTGGCA[C/T]TGGATACCAGAATGA	80196
rs373273712	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398173	GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA	80196
rs373330201	snp	C/T	0.000153988	0.00877328	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417926	GGTACGAGGGGGTAA[C/T]TAATTACACCCAGGG	80196
rs373551359	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403117	AATAGGATAAAGAGG[C/T]CGGGCGCGGTGGCTC	80196
rs373568534	snp	A/G	4.95954e-05	0.00497948	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420743	TAGAGAAAGTAAACC[A/G]GTTATACAAAGAGAA	80196
rs373607538	snp	C/T	0.0107246	0.0724382	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411592	GTGTCATTTGAGATT[C/T]TTGGTTTTCTTTACC	80196
rs373649845	snp	A/G	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413288	TTCCTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	80196
rs373654787	snp	A/C	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421827	AAATCTTATGTTCCT[A/C]TCTAGCTTAAACAGC	80196
rs373863873	snp	C/G/T	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414343	TTCTAAACACTATAG[C/G/T]TTTTATTTTAAGCAT	80196
rs373896354	snp	G/T	3.31087e-05	0.00406857	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402753	AAAGGTGGGGGAGTG[G/T]TACTAAGGATCAAGT	80196
rs373942453	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407042	ACAGTACCCAACAGT[C/T]AGTTTTTCACCCCTT	80196
rs373966078	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402695	AGATATCAAGGAGAA[A/T]GTAATCTACTGAATG	80196
rs374047813	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399823	CCTCAGGGACGCTAT[C/T]TCCCATTTCAAACAC	80196
rs374173829	snp	C/T	1.6507e-05	0.00287284	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402850	ATTGTAATAATCGAT[C/T]AGTTTGGCCAATGTC	80196
rs374432244	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408070	CAGTGATTTGGGAGG[A/C]TGAAGCAGAAGGATC	80196
rs374454541	snp	A/G	0.000153988	0.00877328	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416356	AGCCTGTGGGCTTTC[A/G]TTTTCAGTCTTTAGA	80196
rs374643962	snp	A/G	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410966	TTGAGACAGGGTCTC[A/G]CTCCGTCACCCAGGC	80196
rs374654278	in-del	-/CT			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398901	GTGGCCTGCCACGCA[-/CT]CTCTCTCTCTCCGTG	80196
rs374677569	snp	A/G	0.000307953	0.0124049	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423615	GTCACCCCCAAACTT[A/G]ACCCCCAACATTTCA	80196
rs374827363	snp	G/T	1.65045e-05	0.00287263	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402838	ATAGCACATGTTATT[G/T]TAATAATCGATCAGT	80196
rs374975607	snp	A/G	0.000437904	0.0147905	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400119	TCCCGGGGCGCGGTA[A/G]TCACCGCCCAGAGGG	80196
rs375023523	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413866	AGGTGTGAGCCACCG[C/T]GCCCGGCTTCACCTG	80196
rs375145025	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409277	GGACCACAACACTTG[A/G]CCAAAACTTAGCTGA	80196
rs375234075	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406843	ATTCTCTTATTCTCT[A/G]TGTTGTTTTAAACTA	80196
rs375326843	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409128	TGGACCACAGGCGTG[C/T]ACCACCATGCCCGGC	80196
rs375341078	snp	A/G	1.75906e-05	0.00296564	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417950	CCCAGGGCCCGGCAC[A/G]CTTATTCTTGGCCGT	80196
rs375421973	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414891	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCATGGT	80196
rs375473478	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407682	AAAGAAAAATAAAGG[A/T]ATACAGGCTAATTTA	80196
rs375539157	snp	A/G	0.000437904	0.0147905	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400160	GCAGTGTGAGGAGCT[A/G]CTATGGTGCTGAGTT	80196
rs375929001	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420684	GGAAATTCTGGCTCG[A/G]AATTTTGTCAACTAT	80196
rs376080046	snp	C/G/T	6.58908e-05	0.0057395	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417690	CCCATAGATACTTGT[C/G/T]GTGAGAAAGAAGACT	80196
rs376390193	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403414	AAAAAAAAACCAAAA[A/C]AAAAAAAAAAAAGGA	80196
rs376437787	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405787	CCGTGTCCGGCCTCT[A/G]TCTTATTTCTTTTTT	80196
rs376542969	snp	A/G	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413089	GGAGTGCAATGGTGC[A/G]ATCTAGGCTCACTGC	80196
rs376656619	snp	A/C	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418429	GTGAGGTCCTTGGAC[A/C]TCCTGATTGAATAAC	80196
rs376706808	snp	C/T	6.73911e-05	0.0058044	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423504	TACCTGCACCAAGTG[C/T]GGCAAGCGCATGAGT	80196
rs376707194	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413414	TATAATTTTACCTGT[C/T]CTTTTTTTTTTTTTT	80196
rs376734127	snp	C/T	0.0107246	0.0724382	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401921	AGTTATAAATGATGC[C/T]TTTGTTTTTGTGAAA	80196
rs376776911	snp	A/C	0.0107246	0.0724382	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398148	GGAGGCCGAGGTGGG[A/C]GGATCACGAGGTCAG	80196
rs376909182	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405998	CGGGGTTTCACCATG[C/T]TAGCCAGGATGGTCT	80196
rs377017432	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420289	AGATGATGATGACGA[C/T]GATGATGAGGATGAT	80196
rs377078507	snp	C/T	1.72074e-05	0.00293316	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423561	GGTGCGAGCCGTGCA[C/T]GTGTTCAAGTCCTGA	80196
rs377206024	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416213	CTGAATGAAGTCATG[A/G]GAACTGGAGCTGTCA	80196
rs377270647	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423784	GACACGTGAGCTTCC[C/T]GGGCTCAGCTGGGCT	80196
rs377330563	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419946	GTGCTGTCCCATATC[C/T]TTAATGGCTTTGGCA	80196
rs377368194	in-del	-/GA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409978	TGACCAACATGGAGA[-/GA]AACCCTGCCTCTACT	80196
rs377482605	in-del	-/T	0.00350982	0.0417443	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402732	TTTTCCTTTTTTTTT[-/T]CTCTGAAAGGTGGGG	80196
rs377499687	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413385	GTATATAATCATTTA[A/G]AGGTATGGACTGTTA	80196
rs377505318	snp	C/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398401	TTTTTTTTTTAAGAA[C/T]TGTCAGGCATTTTCA	80196
rs377505774	snp	C/T	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407301	AACTGTAGGGTTTTT[C/T]TCCCCCAATGAACAA	80196
rs377533837	snp	C/T	0.000153988	0.00877328	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417937	GTAACTAATTACACC[C/T]AGGGCCCGGCACGCT	80196
rs377619856	in-del	-/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398607	GTGCTTATTAACTCT[-/G]GAGGTAGACCTGCCA	80196
rs377629063	in-del	-/A	0.0154538	0.0865337	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418361	TGAAAGAGCCATCTG[-/A]ATTAGTGAAAAAATG	80196
rs377645969	snp	A/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410637	ATTTCTGAACTTTCC[A/G]GAAGGCTGGAGTGTT	80196
rs386767036	multinucleotide-polymorphism	CA/TG			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409331	AACCAAAGTGGGATG[CA/TG]AAATACTACATATCC	80196
rs397850094	in-del	-/C			intron-variant, frameshift-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417644	ACTGAAGGTGAAGGA[-/C]CTGCGGCAGTATCTC	80196
rs397963490	in-del	-/TTG			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405408	TATTATCCAGACTTG[-/TTG]GCTACAGAGCTAAGG	80196
rs398098552	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406459	CCTGACTAATTTTTT[-/T]GTATTTCAGTAGAGA	80196
rs527273232	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400301	CTCCTTTCTTTCCGC[C/G]TTAGCGGTTACCTAG	80196
rs527296454	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407483	TGACTGCAAATGCAG[A/G]AGCCAAAGGCATATG	80196
rs527309225	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415801	AATTTTTAGTATATG[C/T]ATATCCCAAATATAC	80196
rs527332802	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401190	GCTGGTCACAGAAAT[G/T]CAGCACATGTTTTGT	80196
rs527338372	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415210	CAAAAAAATCTAGAG[A/T]GAGTTTCAGTTGGTG	80196
rs527477378	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422156	TACTTTGCGGCGTAG[A/G]ATATAACATGGTTGT	80196
rs527829751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406356	GCAGTGGCGTGATCT[C/T]AGCTCACTGCAGCCT	80196
rs527829798	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399265	CTGAGGCAGGAGAAT[C/G]CTTTGAACCCGGGAG	80196
rs527867628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405736	TGATCCTCCTGCCTC[A/G]GCCTCCCAAAGTGCT	80196
rs527905830	snp	C/T	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413434	TTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTT	80196
rs527937942	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413023	TGTGCCCAGGCTATT[A/T]TTTTTTTCCTTCCTC	80196
rs527945351	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420412	CTGTGGACATTCGCT[A/C]GATTAGTACAGGATG	80196
rs528021951	snp	A/G	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411721	CAGTCATACCATGGT[A/G]GAAAGAGGAGCAGGA	80196
rs528070903	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419710	TCTAAAGTGTTCTGA[C/T]TGAGAAATTTTAAAA	80196
rs528253912	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398363	GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA	80196
rs528419692	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405094	AAACTGTCATTCCTA[C/T]TCTTACGCAGATTAT	80196
rs528534112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418565	AGGGGGTTATTAAAA[A/G]TAGAGGAAAGCTGGA	80196
rs528862322	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421848	CTTAAACAGCCCTCC[C/T]ATCATTAACTTTTAT	80196
rs528916658	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402882	TGTCTAAAAGTATTA[C/T]ATTTTAGAGTTCATC	80196
rs529016037	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406996	ACGCTAAAGTTTGGG[A/G]TACAGTTGGTCCCGC	80196
rs529106684	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416640	TTTCTATTATGTTTA[C/T]TTCCAAAAGCAAGAA	80196
rs529154386	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415960	AAACAAGAGATCATG[A/G]GTATTGGCAATGCCA	80196
rs529293094	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412365	CCACCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC	80196
rs529430682	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121400762	GGGGCCGCGAACTAG[A/G]GAAGGCTGGATGTGC	80196
rs529512856	snp	A/G	1.98214e-05	0.00314806	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400163	GTGTGAGGAGCTGCT[A/G]TGGTGCTGAGTTTCC	80196
rs529650241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415052	AGTGAGCCGAGATCA[C/T]GCCATTACACTCCAG	80196
rs529671435	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414314	GAATTAGGACAAAGG[A/C]AAAAGCCTATTCGTT	80196
rs529685193	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422138	GCCATTCCCACCCTT[A/G]AGTACTTTGCGGCGT	80196
rs530061643	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398551	ATCCATGGATTTGAT[G/T]TGCATTTCCTTGATA	80196
rs530092259	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399179	AACACAGTGAAAACC[A/C]GTCTCTACTAAAAAT	80196
rs530170124	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413338	GGCCAGATTTTCATG[C/T]TTTTAAGCACACCAT	80196
rs530307748	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412898	ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC	80196
rs530347549	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419698	AGATTTGTGTTTTCT[A/G]AAGTGTTCTGATTGA	80196
rs530401918	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418528	AACAAATTTTTTCAC[A/G]CTTAATTTTCTTCTC	80196
rs530839243	snp	G/T	1.65231e-05	0.00287424	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417871	TTCAGGGAGAGCTTA[G/T]GGATGGAGACCAAAC	80196
rs531081110	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414332	AAGCCTATTCGTTCT[A/G]AACACTATAGCTTTT	80196
rs531162515	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423774	TCTGCCTGTGGACAC[C/G]TGAGCTTCCCGGGCT	80196
rs531194831	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401481	TGAAGTATGAGGATA[C/T]TGTAAAAGCTTATTT	80196
rs531346080	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409180	AGACGGGGTTTTACC[A/G]TGTTGGCCAGGCTGG	80196
rs531386204	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416521	TTTCCATCTAGAAAA[A/G]TACTTAATTGGAGGG	80196
rs531433780	snp	C/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423017	AAATTCCAATAGCAT[C/G]CTGACTCCAAAGCCC	80196
rs531521434	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415913	GGGAGGTTTTTTGTT[A/C]TGTAAAATTTGGATC	80196
rs531599397	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422352	CCTGACAAGATACTG[G/T]CTCCTCTGCTTTCCT	80196
rs531787629	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407278	TTGGGCTTTATTCAC[G/T]GAGGAGTAACTGTAG	80196
rs531789356	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407840	TATGGTAACTGGGTT[A/C]CAAGGAAATATAACA	80196
rs531846866	snp	A/T	0.0248432	0.108648	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414168	TTTTACATGCTATTA[A/T]AAAATGTTTGACAGA	80196
rs531910098	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399893	GCCCAGGTCCGCAGG[A/T]CTTCGCTCGGGGCGG	80196
rs531969313	snp	G/T	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413520	GGGTTCAAGCGATTC[G/T]CCTGCCTCAGCCTCC	80196
rs532006940	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420518	GGCCAGTGATGAGTT[C/T]AGAGTGGGGAGGGTC	80196
rs532311942	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398395	AAAAATTTTTTTTTT[A/T]AAGAATTGTCAGGCA	80196
rs532415138	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404309	ATGGCACCTGGCCTA[C/G]TTGTCTGTTTTCATA	80196
rs532448868	in-del	-/GGG	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416911	TTCTGAAATACTTAA[-/GGG]GGAAAAAAAATGTTA	80196
rs532472791	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403645	CTGGACATATAGTGG[G/T]TGAGTTCTCTGAGGA	80196
rs532514962	snp	C/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404910	GCTGAACCTTGAGGC[C/T]ATTTGAAAATCCTGG	80196
rs532561720	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412740	TTTTTTTTTTTTTTT[C/T]TTGAGATGGAGTCTC	80196
rs532752292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419120	GATAGACCACATACA[C/T]GGCAGTGGTTCTGTA	80196
rs532789510	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418624	CTTGGCAGGCTGAGG[C/T]AAGAGGATTGCTTTA	80196
rs532960766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402942	AATGGTATGAGAGAA[A/G]TAATTTAGGATGTAG	80196
rs533134411	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410850	TAGTATTTGGCTGAC[A/T]GTAGTTAATATGTGT	80196
rs533153209	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416792	ACTCTTTAGAGATTC[A/G]ACATCAAATACTTAG	80196
rs533191154	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423714	AAGTGGGGACAGAAA[C/G]ATCCATCCTGAGTTG	80196
rs533557952	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400003	GTGACCGGCCTCCCG[A/G]AAGTCGGCTTCCTAT	80196
rs533605067	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406590	CCGCGCCGGGCTGGT[G/T]TTAAGTTTTTAAATA	80196
rs533842380	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419375	ACACATTACTCAGAA[C/T]GTCTCCTAGTCGTCA	80196
rs533948661	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422096	CATAAATGTAAATAG[A/C]AACTATGTACAGTGC	80196
rs534053105	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420882	ATTTTTGAGAAAGCT[A/G]TGTACCATTTTACTG	80196
rs534090055	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424306	TTTTCAGTGCTACCC[A/G]CTAGCTGATTTTAAC	80196
rs534144227	snp	A/G			intron-variant, splice-acceptor-variant	RNF34, KDM2B	GRCh38.p7	12:121402741	TTTTTTTCTCTGAAA[A/G]GTGGGGGAGTGGTAC	80196
rs534393092	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418812	TGCAACCTCTGCCCC[C/G]CTGGGTTCAAGCAAT	80196
rs534409955	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405166	TTGCTCCTACAGAGG[C/G]GAGGGGGCTTCTAAT	80196
rs534410058	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398232	AAAAAACTAGCCGGG[C/T]GCGGTGGCGGGCGCC	80196
rs534447804	snp	G/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404531	AGCTGGGACTACAGT[G/T]GTGCACCACCACACC	80196
rs534749271	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402568	GGATTAAAAAAAAAA[A/G]TCCAAATTGGTGCCC	80196
rs534884139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409494	CAGCTGAAACAGTGT[A/G]GGCAGGAAGAAGACA	80196
rs534940579	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417174	GGAAAAGACCAGGAA[A/G]TGTGATTCTGCTTTC	80196
rs534977403	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423986	GTGTCCACAAGTGGC[C/T]GACATGGAACATGCT	80196
rs535074870	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410366	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	80196
rs535216026	snp	A/G	3.59479e-05	0.00423942	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417964	CGCTTATTCTTGGCC[A/G]TATATGGTGGGGCCT	80196
rs535514291	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422436	ACTCTGATTTCATCT[C/T]GAGTTGCCTAGTGCC	80196
rs535611735	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406244	TCTGAGGCAGTCCAG[C/G]CAGGTTTTAGAATTT	80196
rs535639770	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400942	CAACCCGATCACTGA[A/G]AGTTCTGAAGAGCTT	80196
rs535678224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408405	CAAGATCATACCACC[A/G]CACTCCAGCCTGGGT	80196
rs535703945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407711	TAACTGGAGGAAGAT[C/T]TTAAAGTATAGGGAA	80196
rs535742857	snp	C/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402033	TGTGGGTATGCTCAT[C/G]TGTAGATTTCTGGGC	80196
rs535875353	snp	C/T	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414758	GATCACAACAATCTC[C/T]GCCTCCCGAATTCAA	80196
rs535876851	snp	A/G	0.00438332	0.0466095	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405956	CTGCTACCACGTCCA[A/G]CTAATTTTTTGTATT	80196
rs535910696	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413670	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	80196
rs535912618	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405329	CTCACATTTGTCTTC[C/T]TGTAGTGAAGATGGA	80196
rs535948816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413142	GCGATTCTCCTGCCT[C/T]GGCCTTCCAAGTAGC	80196
rs536213548	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413328	CACTGAGCCTGGCCA[A/G]ATTTTCATGCTTTTA	80196
rs536489502	snp	A/T	1.86879e-05	0.00305673	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420211	ATACAGATTGATTCC[A/T]GACCTAATCAGATAC	80196
rs536709655	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398200	AACACGGTGAAACCC[A/G]TCTCTACTAAAAATA	80196
rs536876100	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412148	CTCACTGCAAACTCC[A/G]CCTCCTGGGTTCAAG	80196
rs536914107	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411290	CTTCATTTTCTTTCT[C/G]GGGAACAAAGAGGAA	80196
rs536956148	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418757	GCAGAGTCTCACTCT[A/G]TTGCCCAGGCTAGAG	80196
rs537087822	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418254	TTATGTGTTAGTGCA[C/T]GTGTTTCAGTGACCA	80196
rs537114455	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408744	AAAACACTTTGAACA[A/G]TGGCTGCTTTTGATA	80196
rs537289756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423335	CTGGGAGGGTGGCTG[A/G]CTGACTGGCCATGCC	80196
rs537333760	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410045	CTGTAATCCCAGCTA[C/T]TAGGAGGCTGAGGCA	80196
rs537504031	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400404	GCTGCCGGACCCTCT[C/G]GAGCTCCTCCAGTGC	80196
rs537636270	snp	A/G	1.64735e-05	0.00286993	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416170	TTAGGCGGGTGCCAC[A/G]TCTATGTGGGCTTCG	80196
rs537778311	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410743	GGGAGATCATGTTCT[C/T]ATTGGAAGATTTTGC	80196
rs538042011	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400057	CGCTTTTACCGGGGC[A/G]CGCGGCGAGCGTGAC	80196
rs538065666	snp	C/T	0.000174688	0.00934416	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415281	TGCTATAGTATATTA[C/T]ACCCAATTACAAATG	80196
rs538080699	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399366	ATAAAAAAAAGGTGT[A/G]GGAAAATAAACTGTC	80196
rs538140958	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421760	TTGCCCAGACTAGTG[A/C]TGAATTAGGCGTGGG	80196
rs538273518	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413056	TTCGAGGCAGAGTCT[C/T]ACTCTGTCACCCAAG	80196
rs538292340	snp	G/T	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404615	AGGCTGGTCTTGAAC[G/T]CCTGACCTCAAGTGA	80196
rs538310229	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419898	CAGGCTCCAGTTAAA[C/T]TAGCCATTTGCAGGT	80196
rs538310409	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412396	AGGTGCCCGCCACCA[C/T]GCCAGGCTAATTTTG	80196
rs538349327	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419335	GTACACTGTGATGTT[C/T]GCACAATGACAAAAT	80196
rs538989285	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419977	TTCCATTATGGGACC[C/T]TCCTGAGAGAGTTAA	80196
rs539222818	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411092	GCACATGCCACCACA[A/C]CTGGCTAATTTTATT	80196
rs539342428	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417267	TTTAATTCATTAACA[A/C]AAGAGTGTGTTTTTC	80196
rs539448073	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408579	GTAGAGATGCCTTTG[C/T]CCTGAGGAGGCATGC	80196
rs539486553	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416053	AATATAGTAATCTCA[A/G]AGTTATTGAGGGCAA	80196
rs539519797	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423238	AACCAAAGTGCAGAG[A/G]AGTTGGGATTATTTC	80196
rs539521866	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412821	CCTCTGCCTCCTGGG[C/T]TCAAGTAATTCTCCT	80196
rs539877379	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417204	CTGCTCTGTGTGGTT[C/T]AAGCTCTGTTTTGTT	80196
rs540029238	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399047	AAATACTGGTTAAGT[C/T]AGAGGTGAGATTAAA	80196
rs540081406	snp	A/C	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405471	CAAACATTTTAATTT[A/C]CATTTGTCTTCTTGC	80196
rs540130898	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413182	AGGCATCTGCCAATA[C/T]GCCCAGCTAATTTTT	80196
rs540172137	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417143	TGCTCTTTAAATGGA[A/G]GAAATTGTTCATGTA	80196
rs540231602	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399922	GGAAAAGAATCCTCC[C/G]CGCGCACTCCCAGCC	80196
rs540470027	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421108	CTAATGCCTTTGGCC[-/G]GGCCAGTACCTTGGT	80196
rs540532499	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412707	AAATTAACTCTTAGT[C/G]AATCTAGATGTTCAT	80196
rs540672550	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419498	ATAAGGCACAGCTGA[C/T]TTACATACCCCTTTT	80196
rs540784278	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423093	TAATATATCCCTATC[A/T]CAGATGTCTTGAATT	80196
rs541018409	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403757	AAAACTTCTAGGTTC[A/T]TCCTTAAAATAACTG	80196
rs541055430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403264	AGCTGGATGTGGTGG[C/T]GGGCGCCTGTAGTCC	80196
rs541217333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401326	TATTTGTAAGTAACC[A/G]TATTACAAGGCAGAA	80196
rs541255451	snp	C/T	0.0023933	0.0345097	intron-variant	RNF34	GRCh38.p7	12:121400778	GAAGGCTGGATGTGC[C/T]TCCATCGCCACTAGG	80196
rs541296878	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408131	GGCAGCATATCAAGA[C/T]CCCGTCTCTAAAAAA	80196
rs541370805	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415593	TGTACTCCAGCCTGG[G/T]TGACAATGAGACCCT	80196
rs541374474	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411222	TGTGAGCCACCATTC[C/T]TGGCCTGTTTTTAAT	80196
rs541509653	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422759	TCATCGTCTTTCTTA[C/T]TCACAGACTGGATTT	80196
rs541894466	snp	C/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422151	TTAAGTACTTTGCGG[C/T]GTAGGATATAACATG	80196
rs541930136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413918	TCTTGAGAATTATAG[A/G]GTGTGAAGACTTATA	80196
rs541967110	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421092	AAATGCTTATTTTCT[A/C]ACTAATGCCTTTGGC	80196
rs542072626	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412164	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	80196
rs542101589	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400101	TCCGGACGCTCGGTC[G/T]CCTCCCGGGGCGCGG	80196
rs542237745	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406982	GGGTATATTGAGTGA[C/T]GCTAAAGTTTGGGGT	80196
rs542272806	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406339	GTCGCCCAGGCTGGA[A/G]TGCAGTGGCGTGATC	80196
rs542290556	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398972	TATAATGTATATAAA[C/T]AACAGAACAGTCTTA	80196
rs542350542	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413346	TTTCATGCTTTTAAG[C/T]ACACCATGGCTGTAG	80196
rs542407829	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404752	CTGGCTGGTTGATAA[C/T]ATATTTAATGGAATC	80196
rs542442994	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404181	TTTTTTTTTTTCTTC[G/T]TATTTAGTAGAGACG	80196
rs542445003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412535	GGGGTGAGCCACCAC[A/G]CCTGGCCTAATTTTT	80196
rs542768426	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405480	TAATTTCCATTTGTC[G/T]TCTTGCTTTTTTTTT	80196
rs542816906	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407018	TGGTCCCGCCAGCAG[A/G]TAGTGAACACAGTAC	80196
rs542907333	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403240	TCTCTACTAAAAATA[C/G]AAAAAATTAGCTGGA	80196
rs542914194	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418911	GGGGTTTCACCATGT[C/T]GGTCAGGCTGGTCTC	80196
rs543410838	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406649	CAGGCAGACCATGGT[C/T]CTATGGTGGCTCTAC	80196
rs543435955	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405908	ACGCCATTCTCCTGC[C/G]TCAGCCTCCTGAGTA	80196
rs543515213	snp	C/T	0.00279162	0.0372561	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408055	TCATGCCTGTAATCC[C/T]AGTGATTTGGGAGGC	80196
rs543520616	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424379	CTTGGTCAGTTCCTA[A/C]ATCAAGTGACCTGGC	80196
rs543522964	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400726	TGCCACCCGGAAGGG[C/G]TGCTTCGTAGGCTGC	80196
rs543550025	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416560	ACTGCTCAAGTTTTA[C/T]AGACATTGTTTCTCA	80196
rs543650240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415540	AGAATCGCTTGAACC[C/T]AGGAGGTGGAGGTTG	80196
rs543778079	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422103	GTAAATAGCAACTAT[A/G]TACAGTGCACAACGA	80196
rs543904299	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400157	TCGGCAGTGTGAGGA[G/T]CTGCTATGGTGCTGA	80196
rs544074648	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422645	GTTCCAACTATTCAT[C/G]ATTCCCTTTGATCTC	80196
rs544095678	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413663	GCTCACTGCAAGCTC[C/G]GCCTCCCGGGTTCAC	80196
rs544113736	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399664	CATGAACGCGGGAAC[A/G]TCTGGGAAGGAAATC	80196
rs544151049	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406269	GAATTTGATTTCTTA[C/T]TATGGAATGTGTAAG	80196
rs544466350	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399156	AGGAGTTCTAGACCA[C/G]CCTGGCCAACACAGT	80196
rs544505005	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405510	TCTTTTTGAGACAGG[G/T]TCTTGCTCTGTCACC	80196
rs544658836	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413225	AGAGACGGCGTTTCG[A/C]CATGTTGTCCAGGCT	80196
rs544697639	snp	C/T	5.69071e-05	0.00533388	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420322	TGATGAAGAAGAAAA[C/T]GCAGAGGATCGGGTG	80196
rs544697783	snp	A/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412756	TTGAGATGGAGTCTC[A/G]CTGTGTCACCCAGGC	80196
rs544786415	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403303	CTGGAGGCTGAGGCA[A/G]GAGAATGGCGTGAAC	80196
rs544791890	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418365	AGAGCCATCTGAATT[A/C]GTGAAAAAATGTAGT	80196
rs544840841	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411864	TAGTAGGAAGCTAAA[C/G]TTGTAAAACTGCACT	80196
rs544843564	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418869	TAGGATTACACCCCA[A/G]TTAATTTTTGTATTT	80196
rs544957295	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424633	GGAGGATGGCTTGAG[C/T]CTTGGGTGTGGAGGT	80196
rs545020514	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398269	CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	80196
rs545076929	snp	A/G			intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417568	TACAAGAAAATCTCC[A/G]TAGATGTTCTACTTG	80196
rs545229348	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121400313	CGCCTTAGCGGTTAC[C/T]TAGTCGTCATCTCGG	80196
rs545379395	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409040	GCAGTGGTACAGTGG[C/T]GTGATATCTGCTCAC	80196
rs545596191	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405704	GACCAGGCTGGTCTG[A/G]AACTCCTGACCTCAG	80196
rs545893040	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423423	GGATGAGGAAGACGA[C/T]AGCCTGTGTCGCATC	80196
rs545927737	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422880	GATTCTAAGGCTAGG[C/G]AGGGAAGGATGCACA	80196
rs545992841	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414822	TGGGAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT	80196
rs546221864	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423640	ATTTCAATGCACAGA[A/G]GGGACTGGAAAGTTA	80196
rs546453476	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398100	ATTTTTGGGCCGGGC[A/G]CGGTGGCTCACGCCT	80196
rs546490493	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404224	GTTGCCCAGGCTGGT[C/G]CCAAACTCCTGAGCT	80196
rs546639457	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403456	CTTTTTTATCAACTG[G/T]TTTTTCTGCTTTGCT	80196
rs546726587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411847	TGGTTTAGTAGCTAC[A/G]TTAGTAGGAAGCTAA	80196
rs546990930	snp	A/G			intron-variant	RNF34	GRCh38.p7	12:121401470	GAACTGTGCCTTGAA[A/G]TATGAGGATATTGTA	80196
rs547046076	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411057	CTTTTGCCTCAGCCT[C/T]CGAGTAGCTGGGAGC	80196
rs547310761	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423687	CTATTTTAAAACATT[A/G]TTTTGACTACTAAGT	80196
rs547313369	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424307	TTTCAGTGCTACCCG[C/T]TAGCTGATTTTAACT	80196
rs547338011	snp	C/T	0.00438332	0.0466095	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411944	AGTTGAGGTATTTTT[C/T]TCCCCAAAAAATGTA	80196
rs547348227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423100	TCCCTATCACAGATG[C/T]CTTGAATTAGACAAA	80196
rs547399001	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415961	AACAAGAGATCATGG[G/T]TATTGGCAATGCCAG	80196
rs547546223	snp	C/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424579	TTTGGAAAAAATTAG[C/G]CAGGCGTGGTAGTCC	80196
rs547619569	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409289	TTGGCCAAAACTTAG[C/T]TGACCCTTTCTTAAA	80196
rs547687687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407421	GCCTAGTATACTGTC[A/G]GAAGCCAGAGGTGGG	80196
rs547749063	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405203	TTGGGGAGGGAACAG[G/T]ATGGGAGAAACACTG	80196
rs547820821	snp	C/T	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406576	ACAGGCGTGAGCCAC[C/T]GCGCCGGGCTGGTGT	80196
rs547928605	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421971	ATCCTACTTCAAAGA[C/T]GATGTCACAGTGGTA	80196
rs547962647	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414323	CAAAGGCAAAAGCCT[A/G]TTCGTTCTAAACACT	80196
rs548321215	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399188	AAAACCAGTCTCTAC[C/T]AAAAATAGAAAAAAT	80196
rs548327206	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420633	TGACTTGTCAAGCCT[C/T]GATGATGTGGAAGGA	80196
rs548629660	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398559	ATTTGATGTGCATTT[C/T]CTTGATAGTTAATGA	80196
rs548668886	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405617	CCCTTCTGAGTAGCT[A/G]GGATTACAGGCATCC	80196
rs548797351	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408587	GCCTTTGCCCTGAGG[A/G]GGCATGCAGAATAAA	80196
rs548846218	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412914	TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC	80196
rs548885650	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419206	ACACAAATACTTATT[A/T]CTGTGTTATAGCTGC	80196
rs548977121	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412380	GAGTAGCTGGGACTA[C/T]AGGTGCCCGCCACCA	80196
rs549087125	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417020	ATTGTGATTAGGCTG[C/T]GTAGTTTACAGATTA	80196
rs549153257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418478	AATATTTACTTGTAC[A/G]TGAGTGATTCTAAAC	80196
rs549441736	snp	C/G	1.66252e-05	0.00288311	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417900	ACATCCAGATCTGGA[C/G]TGCCGGCACAGGTAC	80196
rs549734944	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410149	ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAG	80196
rs549793312	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401780	TTTTGAATTGAAGTG[A/G]AAGGTACTACTTTCT	80196
rs549908728	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408319	TGATGGCAGGCACTT[A/G]TAATCCCAGCTACTT	80196
rs549987247	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412835	GTTCAAGTAATTCTC[C/T]TGCCTTAGCCTCCCA	80196
rs550042926	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407628	GGTTTGTAGAAGATG[C/T]TTCAATCTTACTATC	80196
rs550045118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415930	GTAAAATTTGGATCA[C/T]GTTCTCTTTTTGTTA	80196
rs550081780	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415290	ATATTATACCCAATT[A/G]CAAATGCGAAAACAG	80196
rs550116853	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413528	GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	80196
rs550156574	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407776	GTCTCTAAAGCTTTT[A/C]AAAGGAGGGTGCAGA	80196
rs550189865	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406529	TGAGCTCAAGCAATC[C/T]GCCCACTTCAGCCTC	80196
rs550280561	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419910	AAACTAGCCATTTGC[A/G]GGTACTTTGATAATG	80196
rs550468683	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405916	CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAC	80196
rs551113250	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412010	CAGTTTTAAGAGTGC[A/G]TACTCTAAAGAACTG	80196
rs551150356	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411166	GACCTGGCCTCAAAC[A/G]ATCCTCCCACCTTGG	80196
rs551402731	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409428	TAGGGCCACAGGCTT[C/T]CAAAGTAACCACAGC	80196
rs551491860	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423247	GCAGAGAAGTTGGGA[C/T]TATTTCTTGTACAAC	80196
rs551632043	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410108	GCGGTGAGCCAAGAT[A/C]GTGCCATCGCACTCC	80196
rs551662505	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412771	GCTGTGTCACCCAGG[C/T]TGGAGTGCAGTGGCG	80196
rs551804664	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400312	CCGCCTTAGCGGTTA[C/T]CTAGTCGTCATCTCG	80196
rs552001630	snp	G/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415221	AGAGAGAGTTTCAGT[G/T]GGTGTTTTGATGTTT	80196
rs552029784	snp	C/T			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417901	CATCCAGATCTGGAG[C/T]GCCGGCACAGGTACG	80196
rs552061403	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121400851	GGAGTGAGAGCGTGG[A/G]AGCATTACTGATGAG	80196
rs552183261	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412506	CCTTGTCCTCCCAAA[C/G]TGCTAGGATTACAGG	80196
rs552352113	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422253	ATCTCTGGCTTGGGT[A/G]GAACACACATTTTGT	80196
rs552464462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420466	CAGTATACTGAAACA[C/T]TTCTAGGACTGCTGA	80196
rs552543818	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405761	AGTGCTGGGATCACA[A/G]GCGTGAGCCACCGTG	80196
rs552570553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413464	TTGCCCAAGCTGGAG[C/T]GCGGTGGCACAATCT	80196
rs552640635	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419296	CTAGGTGTGTAGCAG[C/G]CTGTGCCATCTAGGT	80196
rs552647261	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412340	TGCCTCCCGGGTTCA[C/T]GCCATTCTCCCACCT	80196
rs552849269	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413038	TTTTTTTTCCTTCCT[C/G]TTTTCGAGGCAGAGT	80196
rs552964821	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403783	AACTGTGTAAATAAT[A/C]TATTTAACTTAGAGT	80196
rs553019955	in-del	-/GAGGTATATAATCATTTA	0.0807149	0.183963	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413366	ATGGCTGTAGAGTTT[-/GAGGTATATAATCATTTA]GAGGTATATAATCAT	80196
rs553022776	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411446	GTAGTTGAAAAAAAA[A/T]TTTTCAGCCTAGAAT	80196
rs553035564	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403122	GATAAAGAGGCCGGG[C/T]GCGGTGGCTCACGCC	80196
rs553059394	snp	C/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418832	GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTTCCG	80196
rs553074342	snp	G/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402670	TCTGGGTTCTTCCAA[G/T]CTCAAAATGAGATAT	80196
rs553205364	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410383	CTCTACTAAAAATAC[A/G]AAAATTAGCCGGGTG	80196
rs553219149	in-del	-/A	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414517	AGGGAAGAGACAAGG[-/A]AAAAAACCATAGAAA	80196
rs553418450	snp	C/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416298	ACCCTGAGTTTTCCA[C/G]CTACCCACCAGCAGC	80196
rs553482643	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409531	CTTTGACTGAGCAGG[A/T]CTTAAGCTTTTAACC	80196
rs553768457	snp	G/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424687	CTGAAATCCAACTTG[G/T]GTAACAGAGCCAGAC	80196
rs553999305	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421956	CAAAATATTTTGGCA[A/G]TCCTACTTCAAAGAT	80196
rs554046703	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121400961	TCTGAAGAGCTTTGT[C/G]AACAGCAGTCAGTTC	80196
rs554084808	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400547	GAGCCGCCAGGGCTC[G/T]CCTGAGCCTCGGTCC	80196
rs554086502	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415375	CTTGTAATCTGAGCA[C/G]TTCAGGAGGCCAAGG	80196
rs554182016	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399523	TCAAAGAGCCCTTGG[A/G]ATTTGAGAGCCCTTG	80196
rs554257671	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405366	GTCTCCACTCAACTA[A/C/G]CTGGTAAGCTGCTCT	80196
rs554329296	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419057	GGAAATTTGGTCTAA[C/T]TGCCTTCTAGATATA	80196
rs554382799	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405135	ATTCTTTCCCCTCCC[A/G]TTTGCTTCCTCTCCT	80196
rs554430671	snp	C/G	0.00517822	0.0506191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413143	CGATTCTCCTGCCTC[C/G]GCCTTCCAAGTAGCT	80196
rs554797649	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421631	ACACGATCAAGCCAC[A/G]GAACATTTATGGACA	80196
rs555022639	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418760	GAGTCTCACTCTGTT[A/G]CCCAGGCTAGAGTGA	80196
rs555050713	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422782	CTGGATTTTCTCAGA[A/T]GTAAAGGTGGGCCAA	80196
rs555243879	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424394	AATCAAGTGACCTGG[A/C]CTAGCACCCCTCTTC	80196
rs555279401	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403669	CTGAGGAAGCTTTCA[C/T]TGATGGAAGAACAGT	80196
rs555316463	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403228	AGTGAAACCCTGTCT[A/C/T]TACTAAAAATACAAA	80196
rs555324590	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411328	TCCTTGTATAGAAAC[A/G]TGAGGAATGGGACAA	80196
rs555363388	snp	C/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410544	TCTGTCTCAAAACCA[C/G]CAAAAAAAAAAAAAT	80196
rs555440509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418316	ATGCCCATTTGTCTT[A/G]CTACAGTGAAATTGT	80196
rs555463139	snp	G/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408747	ACACTTTGAACAATG[G/T]CTGCTTTTGATAGAC	80196
rs555501715	snp	A/G	0.00110307	0.0234589	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416231	ACTGGAGCTGTCAGG[A/G]GCCAGCAGTCAGCAT	80196
rs555555558	snp	C/T	0.00318978	0.0398085	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406326	AGACTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG	80196
rs555771925	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF34, KDM2B	GRCh38.p7	12:121402500	TAGGTCTTACCTCTC[A/G]GACTCAAGTAACTTT	80196
rs555823341	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422709	ATAGCCCTATGGCCA[A/G]ATCTCAGGCTGGGGT	80196
rs555865152	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402723	TGTAATTCCTTTTCC[-/T]TTTTTTTTTCTCTGA	80196
rs556023779	snp	C/T	0.000348129	0.0131888	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423357	GGCCATGCCTGAAGC[C/T]GAGGCCTTAGCTCTC	80196
rs556125439	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400091	GCCCCTTACGTCCGG[A/G]CGCTCGGTCGCCTCC	80196
rs556230423	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121400470	CGGGCGTCCCTAGCG[C/T]TCGCGCCGGGTGGGC	80196
rs556378668	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420984	GGCTGCGAGACCACC[A/G]CTGCCAAGTGAGTTA	80196
rs556518285	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414690	TTGTTGTTGTTTTTT[C/T]GAGATGGACTCTCGC	80196
rs556557001	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413870	GTGAGCCACCGCGCC[C/T]GGCTTCACCTGACTT	80196
rs556584334	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398904	GCCTGCCACGCACTC[A/T]CTCTCTCTCCGTGTG	80196
rs556657886	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412433	TTTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	80196
rs556701475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403201	GGAGGTTGAGACCAT[C/T]CTGGCTAACACAGTG	80196
rs556724817	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405306	GGCTCAGTACTTTCT[A/G]GGACCTTCTCACATT	80196
rs556981433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410961	TGTTTTTGAGACAGG[A/G]TCTCACTCCGTCACC	80196
rs556998348	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404714	TGGAAACTACCATAG[C/T]TTTTCTGATTCTTCG	80196
rs557321241	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404553	ACCACACCCAGCTAA[-/T]TTTTTTTTGGTATTT	80196
rs557485368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403132	CCGGGCGCGGTGGCT[C/T]ACGCCTGTAGTCCCA	80196
rs557821046	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416085	CTTACCTCTCCAGAA[G/T]AGCATTCCCTGAGGA	80196
rs557896634	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422588	AAAACATTTCTCTTA[A/C]ATCTAGAGACTACTG	80196
rs558215799	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400024	GGCTTCCTATTGGTC[A/G]TCGTGGCCGCCGCTC	80196
rs558250781	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399645	CCCCGAGGTCATCAC[A/C]GAGCATGAACGCGGG	80196
rs558330013	in-del	-/A	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405681	TAGAGACGGGGTTTC[-/A]CCATGTTGACCAGGC	80196
rs558426432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406096	GCCCGGCCTGTCTTA[C/T]TTCTTAATTAGCTCC	80196
rs558557741	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404907	ACAGCTGAACCTTGA[A/G]GCCATTTGAAAATCC	80196
rs558564784	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413722	AGCTGGGACTACAGG[C/T]CCCACCAGCATGCCC	80196
rs558641438	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406591	CGCGCCGGGCTGGTG[G/T]TAAGTTTTTAAATAC	80196
rs558920463	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420903	CATTTTACTGAGTAT[C/G]AGTTAGTTACATGAG	80196
rs558958221	snp	A/G	3.44489e-05	0.00415009	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420290	GATGATGATGACGAC[A/G]ATGATGAGGATGATG	80196
rs559212100	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410733	TTCTCTCACTGGGAG[A/T]TCATGTTCTCATTGG	80196
rs559243669	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398776	GAAAGGCTTTCTGTA[A/C/G]ATTTTTCCAAAAAAA	80196
rs559265552	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424460	ATGGGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	80196
rs559299836	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423707	GACTACTAAGTGGGG[A/G]CAGAAAGATCCATCC	80196
rs559449494	in-del	-/CAAC			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421385	TAAAAAAAAAAAAAA[-/CAAC]AAAAAAAAAAAAACC	80196
rs559481976	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401423	CTTCTGGCTACAGAA[A/T]GCAAGGAATATTTTT	80196
rs559487139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403265	GCTGGATGTGGTGGC[A/G]GGCGCCTGTAGTCCC	80196
rs559727039	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414162	CCAGCATTTTACATG[C/G]TATTATAAAATGTTT	80196
rs559896971	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415173	ATTAAAATCTATTCT[G/T]GTTTGTCTACAACTT	80196
rs560023039	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408154	CTAAAAAAATAAAAA[A/T]AAATGGCCAGGTGTG	80196
rs560059835	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415798	AAGAATTTTTAGTAT[A/G]TGCATATCCCAAATA	80196
rs560190992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422798	GTAAAGGTGGGCCAA[A/G]AGCCAGGACGGCCCA	80196
rs560193157	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401313	TCAAAAGAAGAGTTA[C/T]TTGTAAGTAACCATA	80196
rs560471513	snp	C/T	0.00478085	0.0486577	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400106	ACGCTCGGTCGCCTC[C/T]CGGGGCGCGGTAATC	80196
rs560481052	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399847	CAAACACCCAACCGA[C/G]AAAGCAGCGCCGCAG	80196
rs560567381	snp	C/T	0.00438332	0.0466095	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406348	GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC	80196
rs560661573	snp	A/C	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413931	AGGGTGTGAAGACTT[A/C]TAATATTGAAATCCT	80196
rs560698486	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421132	CCTTGGTTCTCTCAA[C/T]TTTTAAATCTAACAG	80196
rs560699835	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404756	CTGGTTGATAATATA[C/T]TTAATGGAATCATTA	80196
rs560795713	snp	A/C	0.00199481	0.0315187	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421155	TCTAACAGTAGGGGG[A/C]AAATTCCCTATAGCC	80196
rs560847736	snp	A/T	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412545	ACCACGCCTGGCCTA[A/T]TTTTTGTGTTTTTAG	80196
rs560873975	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411745	AGCAGGAGAAAAAGA[A/G]GTTTTTGTCCATGAG	80196
rs560910665	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410995	GCTGGAGTGCGGTGG[C/T]GTAAGCATAGCTCAC	80196
rs561190929	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407433	TCAGAAGCCAGAGGT[-/G]GGGGGTATGCCTAGT	80196
rs561412769	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424069	CTAACATTTGATGAA[C/T]GTAAGTTTCCACATT	80196
rs561455551	in-del	-/T	0.00706837	0.0590273	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420811	TTTTTCCCTGTAGTA[-/T]TTTTTCCTTAGGCTT	80196
rs561575037	in-del	-/TT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412231	CATGCCCAACTAATC[-/TT]TTTTTTTTTTTTTTT	80196
rs561619970	snp	A/C	6.60164e-05	0.0057449	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402851	TTGTAATAATCGATC[A/C]GTTTGGCCAATGTCT	80196
rs561803185	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409206	GCTGGTCTCAAACTC[C/G]TGTCCTCAGGTGACC	80196
rs561873903	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423071	TTTCTTTTTCTAGTT[A/G]CAGAAGTAATATATC	80196
rs562033009	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411262	TATAATGAGGGCTAA[A/G]TTAAGTGTTTTTCTT	80196
rs562141916	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423692	TTAAAACATTATTTT[A/G]ACTACTAAGTGGGGA	80196
rs562356831	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421456	TACTTGGGAGGCTGA[A/G]GGGGGAGGATTGCTT	80196
rs562656629	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399176	GCCAACACAGTGAAA[A/C]CCAGTCTCTACTAAA	80196
rs562781161	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399673	GGGAACGTCTGGGAA[A/G]GAAATCTGAGGCCCT	80196
rs562989707	snp	A/C	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404968	CTGCTCTTGCAAAGA[A/C]ACAGAACACCTTTCC	80196
rs563044413	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419689	AAACTGAAGAGATTT[A/G]TGTTTTCTAAAGTGT	80196
rs563070119	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407532	AGTGAACTGACTGCA[A/G]ATTCGGAAGCCCAAG	80196
rs563255908	snp	C/T	0.00597247	0.0543191	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404013	AGATCATTTAGTTTT[C/T]TGTTTCTTTTTTTTT	80196
rs563285897	in-del	-/AAAAAAAAA	0.492727	0.0598633	intron-variant	RNF34	GRCh38.p7	12:121401354	AAGGCTATAGGTATC[-/AAAAAAAAA]AAAAAAAAAAAAAAA	80196
rs563330029	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412324	GGCTCACTGCAAGCT[C/T]TGCCTCCCGGGTTCA	80196
rs563519344	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415508	GTAATCCTAGTTACT[C/T]GGGAGGCTGAGGCAG	80196
rs563595496	snp	C/T			intron-variant, synonymous-codon	RNF34, KDM2B	GRCh38.p7	12:121408659	TAAAGGAGAGCCAGG[C/T]AGATGGAGTCCAGGC	80196
rs563708245	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424725	CAAAAAAAAAAAAAA[A/G]GAAAAAAAAGAAAAA	80196
rs563945980	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403538	TTATTTTATATCACC[A/G]TTGCTAAGATTTAAT	80196
rs564021654	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408294	AAAAATACAAAAAAT[C/T]ACCAGGGTGTGATGG	80196
rs564026513	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34	GRCh38.p7	12:121401460	GGTAACTTTGGAACT[A/G]TGCCTTGAAGTATGA	80196
rs564067256	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409067	TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAAC	80196
rs564166371	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401592	AAAACCACCCTCTGC[C/T]GTGTTAAGATCCAAA	80196
rs564241770	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422943	GCTCCTTTTCCTACT[A/G]AGATGAGGCTCCAGA	80196
rs564309364	snp	A/G	0.00478085	0.0486577	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414852	TAATCCCAGCACTTC[A/G]GGAGGCCGAGGTGGG	80196
rs564509403	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420490	CTGCTGAGATGGCTG[G/T]GAGAATATTCAGGGC	80196
rs564599430	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400141	CCCAGAGGGAAGGAG[A/G]TCGGCAGTGTGAGGA	80196
rs564602418	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399888	GCCACGCCCAGGTCC[A/G]CAGGTCTTCGCTCGG	80196
rs564619232	snp	A/T	0.0248432	0.108648	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414167	ATTTTACATGCTATT[A/T]TAAAATGTTTGACAG	80196
rs564636012	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407197	AACTAAGGTCCCCAA[G/T]TAGGTCATGAAAGCC	80196
rs564742373	in-del	-/G	0.0023933	0.0345097	intron-variant	RNF34	GRCh38.p7	12:121400341	GGAGAGCTGCGCTGA[-/G]GGGGGGTCGCTTGCC	80196
rs564831922	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398386	CAAAAAAAAAAAAAT[A/T]TTTTTTTTTAAGAAT	80196
rs565065750	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404904	AAGACAGCTGAACCT[C/T]GAGGCCATTTGAAAA	80196
rs565102518	snp	C/T	0.00279162	0.0372561	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412725	TCTAGATGTTCATGC[C/T]TTTTTTTTTTTTTTT	80196
rs565110096	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412092	TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG	80196
rs565181731	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405497	CTTGCTTTTTTTTTC[C/T]TTTTGAGACAGGGTC	80196
rs565287200	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411909	AATGAAGAGAAGTTT[A/T]TCCTGGGAGTACTTT	80196
rs565340310	snp	C/T			intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417646	TGAAGGTGAAGGACC[C/T]GCGGCAGTATCTCAT	80196
rs565878281	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416700	TGATTTACTGTAACT[A/G]TGATTCAGATTCAAG	80196
rs565889491	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400989	TTCAGGGTATTGATT[C/G]ATTTGCCGAACTCAA	80196
rs565958374	snp	C/G	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415405	GTAGGCAGATCACTT[C/G]AGGCCACGCATCTGA	80196
rs565988493	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401916	ATGACAGTTATAAAT[A/G]ATGCTTTTGTTTTTG	80196
rs566045979	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415976	GTATTGGCAATGCCA[A/G]ATATTCTTTGGAAAT	80196
rs566065726	snp	C/G	4.24574e-05	0.00460727	intron-variant	RNF34	GRCh38.p7	12:121400241	GCCGGTGGAGCCGGA[C/G]AGACCCTCCTCGCCA	80196
rs566102452	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399973	CGCCCAATCCCTGTC[G/T]CTTCATTGGCTCTGG	80196
rs566102821	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407467	CAACAACTCAGTGAA[C/T]TGACTGCAAATGCAG	80196
rs566140739	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406582	GTGAGCCACCGCGCC[A/G]GGCTGGTGTTAAGTT	80196
rs566276345	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405983	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	80196
rs566339806	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418847	CTGCCTCAGCCTTCC[A/G]AGTAGCTAGGATTAC	80196
rs566527964	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413687	GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC	80196
rs566564625	snp	C/T	1.71228e-05	0.00292594	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420815	TTCCCTGTAGTATTT[C/T]TCCTTAGGCTTTTAA	80196
rs566637758	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421587	ATACATTGATGAAAT[C/T]TGGCACAGAAATTCT	80196
rs566968792	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399194	AGTCTCTACTAAAAA[C/T]AGAAAAAATTAGCCG	80196
rs567044208	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398229	TACAAAAAACTAGCC[A/G]GGCGCGGTGGCGGGC	80196
rs567057952	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413020	CATTGTGCCCAGGCT[A/G]TTTTTTTTTTCCTTC	80196
rs567079374	snp	C/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404477	TCAGCTTACTGCAGT[C/G]TCCGCCTCAAGTGAT	80196
rs567295692	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403055	CAGCAGTTTTGATAA[G/T]AAATCCTTTCACATT	80196
rs567324827	snp	G/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410259	AATATGCTGCATGGG[G/T]CTGGCGTGGTGGCTC	80196
rs567460066	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409485	GTGATGTCCCAGCTG[A/G]AACAGTGTAGGCAGG	80196
rs567695152	snp	A/G	0.000302867	0.0123021	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417916	TGCCGGCACAGGTAC[A/G]AGGGGGTAACTAATT	80196
rs567734553	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424806	AAGGTTAACTGCTGA[C/T]GTGCTGTTTCTTGTG	80196
rs567861217	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423960	ACTTCTGTCCTCTTT[G/T]GATGAGATCAGTGTC	80196
rs567926125	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415050	GCAGTGAGCCGAGAT[C/G]ACGCCATTACACTCC	80196
rs567955868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419243	TATTCAGTACACTAA[C/T]GTGATGTACGGCTTC	80196
rs568108928	snp	A/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409774	ACTGACAGCAGCTAC[A/G]AAGGTACAGGACTAA	80196
rs568162588	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415939	GGATCATGTTCTCTT[G/T]TTGTTAAACAAGAGA	80196
rs568184110	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400933	GATGATTCTCAACCC[G/T]ATCACTGAGAGTTCT	80196
rs568224604	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408341	CAGCTACTTGGGAGG[C/T]TGAGGCACAAGAATC	80196
rs568273746	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407658	CAGTATGGAAGCAAT[C/G]AATGAATAAAAGAAA	80196
rs568458511	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419930	CTTTGATAATGACAC[A/G]GTGCTGTCCCATATC	80196
rs568476746	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405918	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	80196
rs568571722	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418515	AAGAAATGTTTTGAA[C/G]AAATTTTTTCACGCT	80196
rs568585813	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419004	CAACCGCGCCTGGCC[A/G]AGAGTGTCTTTTAAT	80196
rs568859609	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416089	CCTCTCCAGAATAGC[A/G]TTCCCTGAGGATCCC	80196
rs568934658	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420076	GTAGGTTCTTCATGC[A/G]ATTTTGTAGGGCCCA	80196
rs569279560	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404346	AACTTTCTTTTCCCA[C/T]TCTCCCCCTATACTT	80196
rs569447439	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412111	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGCGCAA	80196
rs569482058	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419189	TTTAGATATGTTTAG[A/G]TACACAAATACTTAT	80196
rs569484009	snp	A/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411285	TTTTTCTTCATTTTC[A/T]TTCTGGGGAACAAAG	80196
rs569620270	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418755	AGGCAGAGTCTCACT[C/G]TGTTGCCCAGGCTAG	80196
rs569650243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410111	GTGAGCCAAGATCGT[A/G]CCATCGCACTCCAAC	80196
rs569726001	snp	C/G	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416836	TCACTAAGATGGAAA[C/G]TCATTCAGAGACCCA	80196
rs569901935	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423316	GTGGCTGCTCAGCTT[C/T]GGACTGGGAGGGTGG	80196
rs569923568	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404743	CGTTCTAGTCTGGCT[A/G]GTTGATAATATATTT	80196
rs569961240	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF34, KDM2B	GRCh38.p7	12:121402305	AAAGAAAAAAAGGAA[A/G]AAAAAAGTTAAGCAG	80196
rs570005587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409451	ACCACAGCCCTTTCC[A/G]CTCAGGAATTTGTGG	80196
rs570098861	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423813	CTTTATCACACATCC[C/T]GTGAACACTCATTGA	80196
rs570168559	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415591	ACTGTACTCCAGCCT[A/G]GTTGACAATGAGACC	80196
rs570517350	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121400370	CCCGGCTTCAGGTGC[C/T]CCAACCGAGCCAGGG	80196
rs570519893	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406714	AAGGGATTAGACTAT[C/G]AAGAACAAGTCATTT	80196
rs570530800	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412140	AATCTTGGCTCACTG[C/T]AAACTCCGCCTCCTG	80196
rs570556065	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407537	ACTGACTGCAAATTC[A/G]GAAGCCCAAGGGCTA	80196
rs570590000	snp	C/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424830	TCTTGTGTCCAGGTA[C/T]TGCGCTAGGTGCTGT	80196
rs570667681	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422301	TCTTTCCTAGCTTGA[C/T]TGGCTCCAAGTCACT	80196
rs570696212	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422157	ACTTTGCGGCGTAGG[A/C]TATAACATGGTTGTT	80196
rs570792463	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405362	TCTGGTCTCCACTCA[A/C]CTAGCTGGTAAGCTG	80196
rs570806194	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421630	AACACGATCAAGCCA[C/T]GGAACATTTATGGAC	80196
rs570822139	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407536	AACTGACTGCAAATT[C/T]GGAAGCCCAAGGGCT	80196
rs571056174	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419324	GGTTTGTGGAAGTAC[A/G]CTGTGATGTTCGCAC	80196
rs571085404	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419224	GTGTTATAGCTGCCT[A/G]CAGTATTCAGTACAC	80196
rs571087595	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405219	ATGGGAGAAACACTG[A/T]CAGTCTCTGCTATGG	80196
rs571126155	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413048	TTCCTCTTTTCGAGG[C/T]AGAGTCTCACTCTGT	80196
rs571155668	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398828	GAAGTGACATTATCT[A/G]AGCAGCACTTGAAGC	80196
rs571238898	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398140	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	80196
rs571558432	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403482	TTGCTTTTAGTTATG[C/T]AGGAAAGTTTAACCT	80196
rs571782647	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410399	AAAATTAGCCGGGTG[G/T]GGTGGTGGGTGCCTG	80196
rs571822272	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410688	TGATAACTATAAGTG[C/G]ATTTGCCCTTCAATA	80196
rs571877949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418022	TCAAGTCATGTGCTG[A/G]AGTGAAGCTTCCACA	80196
rs572055216	snp	C/T	0.00478085	0.0486577	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424041	ACTTTATTAGTCATG[C/T]ATATTTTAAATGCTA	80196
rs572090476	snp	A/G	9.54289e-05	0.00690691	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423415	CAGCTGCAGGATGAG[A/G]AAGACGACAGCCTGT	80196
rs572374805	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406349	CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT	80196
rs572409987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407105	GATTATTGTTCTTTC[C/T]AAACTGTTAGAAAAA	80196
rs572439985	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400111	CGGTCGCCTCCCGGG[G/T]CGCGGTAATCACCGC	80196
rs572514910	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399582	TTTTTAAAGGCCGCG[C/T]CCTAGCGAGTGCAGC	80196
rs572530134	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414034	CAACATTACTTCTGG[A/G]TAATAGCAGAAACAG	80196

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