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
rs572552878	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405433	CTAAGGTTCTGTTCT[C/G]CAGTTGATGCTATCA	80196
rs572646435	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398990	CAGAACAGTCTTAGG[G/T]CCTCATGAAGAGCGA	80196
rs572685125	snp	A/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405372	ACTCAACTAGCTGGT[A/T]AGCTGCTCTTGGTCA	80196
rs573011714	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413170	AGCTGGGATTACAGG[C/T]ATCTGCCAATACGCC	80196
rs573048643	snp	A/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420274	TTCAGCAAACACAGA[A/T]GATGATGATGACGAC	80196
rs573149055	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419433	GATAAGTCCAAGCCA[C/G]GAGTTTTATTATTCT	80196
rs573560314	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411356	CAAAATTGTCCCCCT[C/T]CAAAATTGGTATCTA	80196
rs573608438	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418330	TGCTACAGTGAAATT[A/G]TTCTAATTTAGTTAA	80196
rs573625777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403727	GTAGCATCTGAGACA[A/G]TTATTTTTGAATTTA	80196
rs573708418	snp	A/C	0.000399281	0.0141238	intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402520	CAAGTAACTTTTTAA[A/C]CTTGCAGTAACATCC	80196
rs573719835	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411337	AGAAACGTGAGGAAT[G/T]GGACAAAATTGTCCC	80196
rs573738844	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413415	TAATTTTACCTGTCC[-/T]TTTTTTTTTTTTTTG	80196
rs573759044	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409365	CAACAGAAAAACATG[C/T]AGACAGGTCTTGGGG	80196
rs573772329	snp	A/C	3.29462e-05	0.00405857	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417701	TTGTCGTGAGAAAGA[A/C]GACTTGGTGGATCTA	80196
rs574203979	snp	C/T	4.33154e-05	0.00465358	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423373	GAGGCCTTAGCTCTC[C/T]GTTGCCTTTCAGATG	80196
rs574370245	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416817	ACTTAGCTAACAGTT[A/G]TTTTCACTAAGATGG	80196
rs574587139	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400096	TTACGTCCGGACGCT[C/G]GGTCGCCTCCCGGGG	80196
rs574738251	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424052	CATGTATATTTTAAA[C/T]GCTAACATTTGATGA	80196
rs574828140	snp	A/G	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421067	CTAATTAAATTCCTC[A/G]TCTCTGTAAAAATGC	80196
rs574834467	snp	A/T	0.00159617	0.0282053	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406937	ATTTCAACTTTTAGA[A/T]TTGGGGGTACACGTA	80196
rs574861290	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414691	TGTTGTTGTTTTTTC[A/G]AGATGGACTCTCGCT	80196
rs574871411	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406327	GACTCTTGCTGTGTC[A/G]CCCAGGCTGGAGTGC	80196
rs574905270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405316	TTTCTGGGACCTTCT[C/T]ACATTTGTCTTCCTG	80196
rs574924801	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420340	AGAGGATCGGGTGAG[A/G]CCACCTATAAAATTT	80196
rs575071234	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412531	TACAGGGGTGAGCCA[C/T]CACGCCTGGCCTAAT	80196
rs575111071	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411663	TTTATAATGTTACAT[G/T]GTCTGTGAAGAGATA	80196
rs575140723	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121398933	TGTTTTAATCTAATA[C/T]AGCACAACTTGTCGA	80196
rs575295882	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404751	TCTGGCTGGTTGATA[A/G]TATATTTAATGGAAT	80196
rs575748777	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422489	TCTCATCCCATAGAT[C/T]CTTTCTCCCCAGGTC	80196
rs576056549	snp	C/T	0.000798403	0.0199641	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410490	TGCAGTGAGCCGAGA[C/T]TGCGCCACTGCATTC	80196
rs576095104	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409696	GTCCAACATGCAGCC[A/G]AGGCTGAAAACCATT	80196
rs576216040	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415484	TAGCCAAGTGTGTGG[C/T]GTGTGCCTGTAATCC	80196
rs576251902	snp	A/G	0.00398564	0.0444627	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422643	CTGTTCCAACTATTC[A/G]TGATTCCCTTTGATC	80196
rs576252310	snp	C/T	0.00119737	0.0244387	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414875	GAGGTGGGTGGATCA[C/T]CTGAGGTCAGGAGTT	80196
rs576268689	snp	C/T	0.00358779	0.0422022	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403320	AGAATGGCGTGAACC[C/T]GGGAGGCAGAGTTTG	80196
rs576321768	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401122	GCTGCTAGATTAACG[C/T]TGTCTCCATAAAGCG	80196
rs576368857	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408723	TCCTGGAGGTGAAGA[A/G]GGACAAAAACACTTT	80196
rs576402603	in-del	-/A	0.00438332	0.0466095	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399352	GACCTTGTCAAAAAT[-/A]AAAAAAAAGGTGTAG	80196
rs576528278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408046	CGTGGTAGCTCATGC[C/G]TGTAATCCCAGTGAT	80196
rs576894097	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	RNF34	GRCh38.p7	12:121400054	CTGCGCTTTTACCGG[G/T]GCACGCGGCGAGCGT	80196
rs576933400	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF34	GRCh38.p7	12:121399658	ACCGAGCATGAACGC[A/G]GGAACGTCTGGGAAG	80196
rs576971015	snp	G/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406208	CATTGGATACCAGAA[G/T]GACATGAGGATATCT	80196
rs576972624	snp	A/T	0.0023933	0.0345097	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402893	ATTACATTTTAGAGT[A/T]CATCATCTGTTTTTG	80196
rs577533185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404593	ACCGGGTTTCACCAT[C/T]TTGGCTAGGCTGGTC	80196
rs577570233	snp	A/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403843	AGAGTCTATGGGTTT[A/G]TTATTACATTGCTAT	80196
rs577819925	snp	C/T	0.000399281	0.0141238	intron-variant	RNF34	GRCh38.p7	12:121401425	TCTGGCTACAGAAAG[C/T]AAGGAATATTTTTGG	80196
rs578205815	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408526	CAGTATAGGACACTT[A/C]AAGCACTGTTAGGTG	80196
rs578228067	snp	C/G	0.000399281	0.0141238	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408998	TTTTTTTGAGATGGA[C/G]TCTTGCTCGGTCACC	80196
rs745411327	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413738	CCCACCAGCATGCCC[A/C]GCTAATTTTTTGTAT	80196
rs746245342	snp	C/G			intron-variant	RNF34	GRCh38.p7	12:121400328	CTAGTCGTCATCTCG[C/G]AGAGCTGCGCTGAGG	80196
rs746350761	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402583	ATCCAAATTGGTGCC[C/T]TGTGTTAATTTGATT	80196
rs747056457	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400107	CGCTCGGTCGCCTCC[C/T]GGGGCGCGGTAATCA	80196
rs747093876	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402146	CATTAAAAGCTAAGC[A/G]AGTATACCTGGCCGG	80196
rs747380183	snp	A/C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422507	TTCTCCCCAGGTCCA[A/C/G]ACCAGTAGTCGTGGG	80196
rs747981257	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416383	TAGAAAGAAGGTGAG[C/T]TGGATGAAATGTTAC	80196
rs748168400	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422228	CACTGCATAATCTAA[A/C]CCTAGTTCAATCTCT	80196
rs749148963	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414220	AACTGTATTATTATA[C/T]GCTGCCATTTTAACT	80196
rs749605399	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403058	CAGTTTTGATAAGAA[A/G]TCCTTTCACATTCTA	80196
rs750020705	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415573	GTGAGCCGAGATTGC[A/G]CCACTGTACTCCAGC	80196
rs750156975	snp	A/G	6.58946e-05	0.0057396	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417750	CTAGGCTCTGAGGAC[A/G]ACATGGACACAAGCA	80196
rs750534159	snp	A/C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405862	GCAGTGGTGCAATCT[A/C/T]GGCTCACTGCAAGCT	80196
rs751792028	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405584	CGTCTCCCAGGTTCA[A/G]GCAGTTCTCCTGCCT	80196
rs752736240	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421358	CCTGGGCAACATAGA[A/G]AGATCCCATCTCTAA	80196
rs753125287	in-del	-/GCCATG			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413224	TAGAGACGGCGTTTC[-/GCCATG]TTGTCCAGGCTGTTC	80196
rs753139753	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409943	GGCGGATCATCTGAG[A/G]TCAGGAGTTCGAGAC	80196
rs753331968	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416079	GGCAAACTTACCTCT[C/T]CAGAATAGCATTCCC	80196
rs753638123	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403932	CAAGATAGACTCTTA[C/T]GAGAAGAGTCTATGG	80196
rs754118434	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424016	TGAGCAGTGGCTCCT[C/T]TGAATGTTCACTTTA	80196
rs754375315	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406477	ATTTCAGTAGAGATG[G/T]CGTTTCACCACGTTG	80196
rs754455052	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409812	GTTTCACTGAAGGGC[A/G]GCGGGGGTGGGTGTT	80196
rs754730303	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403948	GAGAAGAGTCTATGG[C/G]ATTATTATTACCTTG	80196
rs755689737	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415594	GTACTCCAGCCTGGT[A/T]GACAATGAGACCCTG	80196
rs755897351	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399657	CACCGAGCATGAACG[C/G]GGGAACGTCTGGGAA	80196
rs756699957	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404533	CTGGGACTACAGTTG[G/T]GCACCACCACACCCA	80196
rs757030775	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421620	CTCAGCTGGTAACAC[A/G]ATCAAGCCACGGAAC	80196
rs757315133	in-del	-/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402179	GCAATAGCTCACGCC[-/T]ATAATCCCAGCACTT	80196
rs757317110	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404108	CAACCTCTGCCTCTC[G/T]GGTTCAAACAGTTCT	80196
rs758332533	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418899	TTTAGTAAAGATGGG[G/T]TTTCACCATGTTGGT	80196
rs758841599	in-del	-/AAC			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413232	CGTTTCGCCATGTTG[-/AAC]TCCAGGCTGTTCTTG	80196
rs759154976	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421156	CTAACAGTAGGGGGA[A/G]AATTCCCTATAGCCC	80196
rs759496408	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413216	ATTTTTAGTAGAGAC[G/T]GCGTTTCGCCATGTT	80196
rs759714259	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414698	GTTTTTTCGAGATGG[A/T]CTCTCGCTCTGTCGC	80196
rs760114118	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405272	ATTGAGGAGTTTCAG[C/T]GAAGGAACTGACATG	80196
rs761059150	snp	A/G	3.29457e-05	0.00405854	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420655	GTGGAAGGAATGAGC[A/G]TGCGCCAGCTGAAGG	80196
rs762215953	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417359	TTCATGGCTTTTGAA[A/G]CATGAAAATACCTCT	80196
rs762688343	snp	G/T			intron-variant	RNF34	GRCh38.p7	12:121400737	AGGGGTGCTTCGTAG[G/T]CTGCACGTCGGGGCC	80196
rs763664819	snp	G/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398886	TTTCAGTCTAAGGAA[G/T]TGGCCTGCCACGCAC	80196
rs764249193	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403949	AGAAGAGTCTATGGC[A/T]TTATTATTACCTTGC	80196
rs764523507	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415297	ACCCAATTACAAATG[C/T]GAAAACAGAGGTTTA	80196
rs765046782	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405569	GCTTACCGCAACCTC[C/T]GTCTCCCAGGTTCAA	80196
rs765799232	in-del	-/CGT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413218	TTTTAGTAGAGACGG[-/CGT]TTCGCCATGTTGTCC	80196
rs766651702	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413183	GGCATCTGCCAATAC[A/G]CCCAGCTAATTTTTT	80196
rs767023354	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403448	AGATTTTGCTTTTTT[A/G]TCAACTGTTTTTTCT	80196
rs767575553	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405672	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	80196
rs767838289	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417418	CACTAAGAACTAAAA[G/T]TAAATTTTAGTAGAA	80196
rs769917409	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419102	AATAATGTTTTGGTC[A/G]GTGATAGACCACATA	80196
rs771294589	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422524	CCAGTAGTCGTGGGC[A/C]ATGAACTAAGACCCC	80196
rs771762729	in-del	-/TT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407353	TAAAGAAGGCACCAC[-/TT]TTTGGAATTGAGGCC	80196
rs772794475	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405078	AACCTTATTGGCTGG[-/A]AAACTGTCATTCCTA	80196
rs773091228	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403537	ATTATTTTATATCAC[C/T]GTTGCTAAGATTTAA	80196
rs774880457	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419904	CCAGTTAAACTAGCC[A/G]TTTGCAGGTACTTTG	80196
rs775149559	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423275	AACACTGGGGTGGCA[C/T]TGGGCCTGCAGGGGT	80196
rs775317969	snp	G/T			intron-variant	RNF34	GRCh38.p7	12:121400630	GTTGGGGACATCGTG[G/T]GACCGAGGAGAACAG	80196
rs775365907	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409169	ATTTTTAGTAGAGAC[A/G]GGGTTTTACCATGTT	80196
rs775441979	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416979	CTTAGTGCCCTCTTT[-/A]AAGCTTCTCTAGTGG	80196
rs776856513	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413208	TTTTTTGTATTTTTA[C/G]TAGAGACGGCGTTTC	80196
rs776946519	in-del	-/TGT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414669	AAAAAAATACTTTCC[-/TGT]TGTTGTTGTTGTTGT	80196
rs777159728	in-del	-/A	0.00253793	0.035532	intron-variant	RNF34	GRCh38.p7	12:121400269	CAATCCTATCCTGCC[-/A]AGGGCACCTGAAGCG	80196
rs777254368	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407415	GGGTATGCCTAGTAT[A/G]CTGTCAGAAGCCAGA	80196
rs777414244	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418995	GGCATGAGCCAACCG[C/T]GCCTGGCCAAGAGTG	80196
rs777819504	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121400027	TTCCTATTGGTCGTC[C/G]TGGCCGCCGCTCTGC	80196
rs778951199	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422143	TCCCACCCTTAAGTA[C/T]TTTGCGGCGTAGGAT	80196
rs780639141	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404550	CACCACCACACCCAG[C/G]TAATTTTTTTTGGTA	80196
rs780728725	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406468	ATTTTTTGTATTTCA[A/G]TAGAGATGGCGTTTC	80196
rs781324081	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404109	AACCTCTGCCTCTCG[G/T]GTTCAAACAGTTCTC	80196
rs781520353	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416532	AAAAATACTTAATTG[A/G]AGGGATTATATTACT	80196
rs781783420	snp	G/T	1.65518e-05	0.00287674	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402760	GGGGAGTGGTACTAA[G/T]GATCAAGTATACTGT	80196
rs781788623	snp	C/T	1.7154e-05	0.0029286	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420818	CCTGTAGTATTTTTC[C/T]TTAGGCTTTTAAAAA	80196
rs781788991	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418865	TAGCTAGGATTACAC[C/T]CCAGTTAATTTTTGT	80196
rs781790379	snp	A/C	1.64754e-05	0.00287009	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416362	TGGGCTTTCATTTTC[A/C]GTCTTTAGAAAGAAG	80196
rs781795598	snp	A/G	1.64735e-05	0.00286993	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417602	CTTATTACAAGAGAC[A/G]GCATTTCAGCGCCCT	80196
rs781796282	snp	A/G	1.84708e-05	0.00303892	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423458	TGGATGCCGTCATCG[A/G]CTGTGTCCTACTGGA	80196
rs781801477	in-del	-/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421377	CCCATCTCTAAAAAA[-/C]AAAAAAAAAAAAAAA	80196
rs781802564	snp	A/G	5.85394e-05	0.00540983	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420326	GAAGAAGAAAACGCA[A/G]AGGATCGGGTGAGGC	80196
rs781810169	snp	A/G/T	0.000130035	0.00806239	intron-variant	RNF34	GRCh38.p7	12:121400262	CTCCTCGCCAATCCT[A/G/T]TCCTGCCAGGGCACC	80196
rs781817053	snp	C/T	1.9344e-05	0.00310993	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423608	CAGGACAGTCACCCC[C/T]AAACTTGACCCCCAA	80196
rs781818253	snp	C/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402043	CTCATCTGTAGATTT[C/T]TGGGCAGAGACTGAT	80196
rs781822735	snp	G/T	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420625	TCACTGTCTGACTTG[G/T]CAAGCCTTGATGATG	80196
rs781825686	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414315	AATTAGGACAAAGGC[-/A]AAAGCCTATTCGTTC	80196
rs781828156	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421946	AGAATATGCACAAAA[G/T]ATTTTGGCAATCCTA	80196
rs781830461	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409608	GTGCCCAGGCTGCAC[C/T]ACAGACCAGTGAAAT	80196
rs781834809	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399883	CTTCCGCCACGCCCA[C/G]GTCCGCAGGTCTTCG	80196
rs781837530	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424265	ATGTGTAATCAGTTT[A/G]CATTGTTTTGTATAG	80196
rs781839357	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407917	CCCATCCCTTGTCCC[C/T]CTCTCCACTGTAAGA	80196
rs781840338	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403247	TAAAAATACAAAAAA[C/T]TAGCTGGATGTGGTG	80196
rs781843715	snp	C/T	1.99249e-05	0.00315627	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400179	TGGTGCTGAGTTTCC[C/T]GGTAGAGCCGGCCGA	80196
rs781845352	snp	A/T	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416216	AATGAAGTCATGGGA[A/T]CTGGAGCTGTCAGGG	80196
rs781849586	snp	A/G			intron-variant	RNF34	GRCh38.p7	12:121401094	TGCTGGGGGTGGGTA[A/G]TCTAGCAGGTGAGCT	80196
rs781851364	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416140	AGCTTTAAACTGTGG[G/T]ATTTGTGTTCCTTTT	80196
rs781853828	snp	C/T	1.69186e-05	0.00290844	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423497	ACATGGTTACCTGCA[C/T]CAAGTGCGGCAAGCG	80196
rs781855288	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403067	TAAGAAATCCTTTCA[C/T]ATTCTAAGGAGCATA	80196
rs781856945	snp	A/G	1.64735e-05	0.00286993	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416348	GTTTGTAAAGCCTGT[A/G]GGCTTTCATTTTCAG	80196
rs781857887	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404883	GATTATACACACACA[C/G]AAGCAAAGACAGCTG	80196
rs781859261	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415781	TTTCAGATGAAAAAC[-/A]AAAGAATTTTTAGTA	80196
rs781859896	snp	C/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416200	GTGCTGTGGGCTGCT[C/G]AATGAAGTCATGGGA	80196
rs781862877	snp	A/G	9.92861e-05	0.00704508	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400165	GTGAGGAGCTGCTAT[A/G]GTGCTGAGTTTCCTG	80196
rs781865188	snp	A/T	1.64757e-05	0.00287012	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417581	CCGTAGATGTTCTAC[A/T]TGTCACTTATTACAA	80196
rs781865204	in-del	-/CACA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418081	CCTGATGTATAGTGT[-/CACA]CTGCTGAGGTGCTAG	80196
rs781867072	snp	G/T	2.19957e-05	0.00331623	intron-variant	RNF34	GRCh38.p7	12:121400267	CGCCAATCCTATCCT[G/T]CCAGGGCACCTGAAG	80196
rs781869526	snp	A/G	1.91247e-05	0.00309224	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423451	ATCTGCATGGATGCC[A/G]TCATCGACTGTGTCC	80196
rs781873284	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402188	CACGCCTATAATCCC[A/G]GCACTTTGGGAGGCC	80196
rs781874488	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424213	GGGCTGCATCTAGCT[G/T]CTTTTATTAGAAGTG	80196
rs781875827	snp	A/G	1.64732e-05	0.0028699	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417753	GGCTCTGAGGACGAC[A/G]TGGACACAAGCAGTC	80196
rs781876092	snp	A/G	0.000173656	0.00931654	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415286	TAGTATATTATACCC[A/G]ATTACAAATGCGAAA	80196
rs781878065	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406563	AAGTGCTAGGATTAC[A/C]GGCGTGAGCCACCGC	80196
rs781878227	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422763	CGTCTTTCTTATTCA[C/T]AGACTGGATTTTCTC	80196
rs781880331	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414629	TAAAAATTATGTTTA[A/G]TATCTTCAGTTTGAA	80196
rs781880399	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411207	TGCTGGGATTACAGG[C/T]GTGAGCCACCATTCC	80196
rs781884055	snp	C/G	1.65072e-05	0.00287286	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402859	ATCGATCAGTTTGGC[C/G]AATGTCTTGTCTAAA	80196
rs781891541	snp	C/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402140	AAATTACATTAAAAG[C/G]TAAGCAAGTATACCT	80196
rs781893046	snp	C/T	1.65323e-05	0.00287505	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420295	TGATGACGACGATGA[C/T]GAGGATGATGATGAT	80196
rs781901877	snp	C/T	1.65696e-05	0.00287828	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417890	TGGAGACCAAACATC[C/T]AGATCTGGAGTGCCG	80196
rs781904596	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421697	TTTAATTGTAAAAAA[A/T]ATATATATGTACTTA	80196
rs781904957	in-del	-/G	1.64741e-05	0.00286998	frameshift-variant, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420623	TTCACTGTCTGACTT[-/G]GTCAAGCCTTGATGA	80196
rs781905745	snp	A/G	6.56879e-05	0.00573059	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423342	GGTGGCTGGCTGACT[A/G]GCCATGCCTGAAGCC	80196
rs781912708	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412070	AACTTTATTATTATT[A/T]ATTTTTTTTGAGATG	80196
rs781913200	snp	A/G	0.000167567	0.00915181	intron-variant	RNF34	GRCh38.p7	12:121400229	TGAAGGTGAGGGGCC[A/G]GTGGAGCCGGACAGA	80196
rs781917741	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407616	AGGAAATGGAGTGGT[C/T]TGTAGAAGATGCTTC	80196
rs781918832	snp	C/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401839	TGGCAATTGAAATTA[C/T]AGAAAAGATACGTAT	80196
rs781924694	snp	C/G			intron-variant	RNF34	GRCh38.p7	12:121400372	CGGCTTCAGGTGCCC[C/G]AACCGAGCCAGGGCA	80196
rs781926683	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416190	TGTGGGCTTCGTGCT[A/G]TGGGCTGCTGAATGA	80196
rs781928373	snp	G/T	3.55688e-05	0.00421701	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417464	CATGCTTTCATAATG[G/T]TTTATATCTTGCTGT	80196
rs781929620	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416077	AGGGCAAACTTACCT[C/G]TCCAGAATAGCATTC	80196
rs781936618	snp	A/G	4.95995e-05	0.00497969	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417877	GAGAGCTTATGGATG[A/G]AGACCAAACATCCAG	80196
rs781939092	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416317	CCCACCAGCAGCTAC[A/G]GAAGGGCCCAACATA	80196
rs781939625	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419325	GTTTGTGGAAGTACA[C/T]TGTGATGTTCGCACA	80196
rs781940964	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409449	TAACCACAGCCCTTT[C/T]CACTCAGGAATTTGT	80196
rs781942399	snp	C/G	3.29832e-05	0.00406085	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417824	TTCGTTTTTTTCAAA[C/G]TATACAGCCCCCTCT	80196
rs781943892	snp	C/T	1.65269e-05	0.00287457	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420540	GGGAGGGTCTGGACT[C/T]ATGGGACCAGGGCTA	80196
rs781944892	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402938	TCCAAATGGTATGAG[A/G]GAAATAATTTAGGAT	80196
rs781945425	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406442	CAGGCACTTGCCACC[A/G]CGCCTGACTAATTTT	80196
rs781945749	snp	C/T	1.6473e-05	0.00286988	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416175	CGGGTGCCACGTCTA[C/T]GTGGGCTTCGTGCTG	80196
rs781953057	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415565	AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGT	80196
rs781956471	snp	C/T	2.14475e-05	0.00327464	intron-variant	RNF34	GRCh38.p7	12:121400249	AGCCGGACAGACCCT[C/T]CTCGCCAATCCTATC	80196
rs781958306	snp	C/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399223	CGGGTGTGGGGCGGG[C/T]GCACGAAGTCCCAGC	80196
rs781958744	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404481	CTTACTGCAGTCTCC[A/G]CCTCAAGTGATTCTC	80196
rs781959840	snp	A/G	1.73453e-05	0.00294489	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417940	ACTAATTACACCCAG[A/G]GCCCGGCACGCTTAT	80196
rs781963154	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420000	AGAGTTAATACTCTG[A/G]TTAGATTTTATAACT	80196
rs781968854	snp	G/T	1.65403e-05	0.00287574	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417528	TGTGACTGCAAGAAG[G/T]ATTTTTGCTCCGTTT	80196
rs781970364	snp	C/T	2.30726e-05	0.00339643	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423420	GCAGGATGAGGAAGA[C/T]GACAGCCTGTGTCGC	80196
rs781984773	in-del	-/TTCTTCAAGGTCCCAGAC	1.64738e-05	0.00286995	intron-variant, cds-indel, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417772	CACAAGCAGTCTGAA[-/TTCTTCAAGGTCCCAGAC]TTCTTCAAGGTCCCA	80196
rs781986943	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414326	AGGCAAAAGCCTATT[A/C]GTTCTAAACACTATA	80196
rs781988288	snp	C/T	1.65105e-05	0.00287315	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417847	CCCCCTCTGCTACTA[C/T]GTCTTCGTTTCAGGG	80196
rs781989497	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423773	GTCTGCCTGTGGACA[C/T]GTGAGCTTCCCGGGC	80196
rs781990387	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407864	TATAACAGAGGCAGA[C/G]TGTGAAGAGCTCAGA	80196
rs781991432	snp	C/G	1.67899e-05	0.00289736	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423540	TCCCATCTGCCGGCA[C/G]TATGTGGTGCGAGCC	80196
rs781992788	snp	C/T	5.1013e-05	0.00505014	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420807	TTCATTTTTTCCCTG[C/T]AGTATTTTTCCTTAG	80196
rs781997639	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407358	GAAGGCACCACTTTG[G/T]AATTGAGGCCAGTGA	80196
rs782000917	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121401708	TATCGAAGGAAAGAA[C/T]TAGAGACAGGTCCAG	80196
rs782013133	snp	C/G	1.65647e-05	0.00287786	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420756	CCGGTTATACAAAGA[C/G]AATGAAGAAAACCAA	80196
rs782015770	snp	A/C			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399026	CTTTTTTATGTTTAA[A/C]ATCTTAAATACTGGT	80196
rs782017510	snp	C/G	2.16242e-05	0.0032881	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423426	TGAGGAAGACGACAG[C/G]CTGTGTCGCATCTGC	80196
rs782019491	snp	C/T	5.26357e-05	0.00512982	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417949	ACCCAGGGCCCGGCA[C/T]GCTTATTCTTGGCCG	80196
rs782023464	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422468	TCTCCATTGGCATAT[A/C]TGCCATCTCATCCCA	80196
rs782026372	snp	C/T	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416287	ATTTACACCAAACCC[C/T]GAGTTTTCCACCTAC	80196
rs782029863	snp	A/C			intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417669	TATCTCATTCTGAGA[A/C]ATATACCCATAGATA	80196
rs782031315	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405632	AGGATTACAGGCATC[C/T]ACCACCATACCTGGC	80196
rs782033115	snp	G/T	1.69942e-05	0.00291493	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417927	GTACGAGGGGGTAAC[G/T]AATTACACCCAGGGC	80196
rs782039121	snp	G/T	2.09264e-05	0.00323462	intron-variant	RNF34	GRCh38.p7	12:121400231	AAGGTGAGGGGCCGG[G/T]GGAGCCGGACAGACC	80196
rs782039888	snp	C/G	1.69836e-05	0.00291402	intron-variant, splice-acceptor-variant	RNF34, KDM2B	GRCh38.p7	12:121417503	GCTTTTCTTTCTTCA[C/G]CATGTTTGCTGTGAC	80196
rs782049545	snp	A/G	1.74619e-05	0.00295477	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417945	TTACACCCAGGGCCC[A/G]GCACGCTTATTCTTG	80196
rs782050623	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420087	ATGCAATTTTGTAGG[G/T]CCCAACTTTTTGGAA	80196
rs782051620	snp	A/G	4.6321e-05	0.00481231	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423421	CAGGATGAGGAAGAC[A/G]ACAGCCTGTGTCGCA	80196
rs782051790	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414374	GGGAAAATGCCTTTG[G/T]CCCTCGCTGAAAATT	80196
rs782052357	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418369	CCATCTGAATTAGTG[A/G]AAAAATGTAGTTATT	80196
rs782055171	snp	C/T	3.29723e-05	0.00406018	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420580	CTGTGGTTTCAGAAC[C/T]CCGGGCTCTCCAAGG	80196
rs782055401	snp	C/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423946	CTCAGATGTTTGAAA[C/T]TTCTGTCCTCTTTGG	80196
rs782055965	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407979	TCTTTTAAATAGTTC[C/T]CCAATTGCTTTTATA	80196
rs782058682	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121401851	TTATAGAAAAGATAC[A/G]TATTTTCAGAAGCAA	80196
rs782059035	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412397	GGTGCCCGCCACCAC[G/T]CCAGGCTAATTTTGT	80196
rs782061310	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407723	GATCTTAAAGTATAG[A/G]GAAGACAGAAATGGA	80196
rs782086917	snp	C/T	9.88338e-05	0.00702902	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416260	ATTTGCAGGAGCCAC[C/T]GGTCCATTCAGATTT	80196
rs782099725	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409171	TTTTAGTAGAGACGG[A/G]GTTTTACCATGTTGG	80196
rs782099773	snp	A/G	8.23879e-05	0.00641772	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416161	TGTTCCTTTTTAGGC[A/G]GGTGCCACGTCTATG	80196
rs782101945	in-del	-/T	1.64808e-05	0.00287057	intron-variant, frameshift-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417812	TTTTTTACACGTTCG[-/T]TTTTTTTCAAACTAT	80196
rs782102408	snp	A/G	2.15038e-05	0.00327894	intron-variant	RNF34	GRCh38.p7	12:121400253	GGACAGACCCTCCTC[A/G]CCAATCCTATCCTGC	80196
rs782104066	snp	A/C			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399315	GAGATCACACTATTG[A/C]ACTCCAGCCTGGGCA	80196
rs782106482	snp	C/T	1.64803e-05	0.00287052	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417811	GCTTTTTTACACGTT[C/T]GTTTTTTTCAAACTA	80196
rs782112773	snp	C/T	1.82227e-05	0.00301845	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423586	TCCTGAAACAGGCTC[C/T]CCTCACCAGGACAGT	80196
rs782114147	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410634	CAAATTTCTGAACTT[C/T]CCAGAAGGCTGGAGT	80196
rs782114728	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406079	ATTACATGAGCCACC[A/G]TGCCCGGCCTGTCTT	80196
rs782117201	snp	C/T	1.69499e-05	0.00291112	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417504	CTTTTCTTTCTTCAG[C/T]ATGTTTGCTGTGACT	80196
rs782117384	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418298	TAGTGTAAGTTAGCC[-/T]TAATGCCCATTTGTC	80196
rs782121780	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421211	AACTATCTGTAGATT[G/T]CTGTGTAAGTCACAA	80196
rs782124184	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404286	TGCTAGGATTACAGG[C/T]TTGAGCCATGGCACC	80196
rs782134256	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407867	AACAGAGGCAGAGTG[G/T]GAAGAGCTCAGAAAA	80196
rs782138638	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416204	TGTGGGCTGCTGAAT[A/G]AAGTCATGGGAACTG	80196
rs782139970	snp	G/T	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416194	GGCTTCGTGCTGTGG[G/T]CTGCTGAATGAAGTC	80196
rs782141810	snp	C/T	3.30077e-05	0.00406236	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420557	TGGGACCAGGGCTAA[C/T]GGATGCTCTGTGGTT	80196
rs782145626	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411088	ACAGGCACATGCCAC[A/C]ACACCTGGCTAATTT	80196
rs782149925	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421180	ATAGCCCAGATGTTA[C/T]ATAGTTCTTAGCATC	80196
rs782152650	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424096	CATTGTTGCTGTTTC[G/T]GCATTTAAACATAAT	80196
rs782153356	snp	C/T	1.64958e-05	0.00287187	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417827	GTTTTTTTCAAACTA[C/T]ACAGCCCCCTCTGCT	80196
rs782154002	snp	C/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399578	CTTGTTTTTAAAGGC[C/T]GCGTCCTAGCGAGTG	80196
rs782154595	snp	A/C	5.03478e-05	0.00501711	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420789	GTCCTGTAGGTTTAT[A/C]TTTTCATTTTTTCCC	80196
rs782158662	in-del	-/TA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416631	CATTTTATTTTCTAT[-/TA]TATGTTTATTTCCAA	80196
rs782160334	snp	C/T	1.64798e-05	0.00287047	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417567	TTACAAGAAAATCTC[C/T]GTAGATGTTCTACTT	80196
rs782167758	snp	G/T			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420298	TGACGACGATGATGA[G/T]GATGATGATGATGAA	80196
rs782170558	snp	C/T	1.99094e-05	0.00315505	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423441	CCTGTGTCGCATCTG[C/T]ATGGATGCCGTCATC	80196
rs782177003	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413316	ACAGGCATAAGCCAC[G/T]GAGCCTGGCCAGATT	80196
rs782178088	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408726	TGGAGGTGAAGAAGG[A/T]CAAAAACACTTTGAA	80196
rs782178280	snp	C/G	1.64969e-05	0.00287196	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416139	TAGCTTTAAACTGTG[C/G]GATTTGTGTTCCTTT	80196
rs782187277	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406827	GGCAGACAGTTGCCT[A/C]ATTCTCTTATTCTCT	80196
rs782188719	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420656	TGGAAGGAATGAGCG[C/T]GCGCCAGCTGAAGGA	80196
rs782191729	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416266	AGGAGCCACCGGTCC[A/G]TTCAGATTTACACCA	80196
rs782192475	snp	A/G	1.64749e-05	0.00287005	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417795	AGGTCCCAGACTTCT[A/G]GCTTTTTTACACGTT	80196
rs782195428	snp	A/C/G	6.26473e-05	0.00559646	intron-variant	RNF34	GRCh38.p7	12:121400230	GAAGGTGAGGGGCCG[A/C/G]TGGAGCCGGACAGAC	80196
rs782197100	snp	A/C			intron-variant	RNF34	GRCh38.p7	12:121400568	GCCTCGGTCCCTTGG[A/C]GCGCGGCGTGCCCTT	80196
rs782201451	snp	C/T	1.71976e-05	0.00293232	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417497	TCAAATGCTTTTCTT[C/T]CTTCAGCATGTTTGC	80196
rs782203826	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417101	GCCTTTCTCTTTCCC[G/T]GTCAGTCTGTTATGC	80196
rs782203874	snp	A/G	3.37684e-05	0.0041089	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423388	TGTTGCCTTTCAGAT[A/G]GCGAGCGGCTGCAGC	80196
rs782204217	snp	A/G/T	5.05798e-05	0.0050287	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417919	CGGCACAGGTACGAG[A/G/T]GGGTAACTAATTACA	80196
rs782205285	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420475	GAAACACTTCTAGGA[C/T]TGCTGAGATGGCTGG	80196
rs782205340	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404117	CCTCTCGGGTTCAAA[C/T]AGTTCTCCTGCCTCA	80196
rs782205927	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415191	TTGTCTACAACTTCA[A/G]GTACAAAAAAATCTA	80196
rs782208010	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407435	CAGAAGCCAGAGGTG[A/G]GGGTATGCCTAGTAT	80196
rs782208714	snp	C/T	2.0253e-05	0.00318215	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400206	CCGAGCTGAGGCGGT[C/T]GCGGCCATGAAGGTG	80196
rs782210356	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416255	TCAGCATTTGCAGGA[A/G]CCACCGGTCCATTCA	80196
rs782212928	snp	A/G	4.22833e-05	0.00459781	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420244	TGTATAAGTGTAGGT[A/G]CAAAGTGAAATCACT	80196
rs782213405	snp	G/T	1.65181e-05	0.00287381	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416414	ATAACAACACACATG[G/T]GTCAGCATTCTTGAT	80196
rs782215452	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412031	TAAAGAACTGTGGAT[C/G]AATCCTTTACTTAAA	80196
rs782215822	snp	A/T			intron-variant	RNF34	GRCh38.p7	12:121401739	TGTTGAAATTTTTAA[A/T]CAAGTTCTTTGAAAA	80196
rs782218789	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410107	TGCGGTGAGCCAAGA[A/T]CGTGCCATCGCACTC	80196
rs782219449	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405452	TTGATGCTATCAGTA[A/G]AAACAAACATTTTAA	80196
rs782220675	snp	A/T	1.64732e-05	0.0028699	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417674	CATTCTGAGAAATAT[A/T]CCCATAGATACTTGT	80196
rs782224495	snp	C/T	1.67685e-05	0.00289551	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423511	ACCAAGTGCGGCAAG[C/T]GCATGAGTGAGTGTC	80196
rs782224901	snp	A/G	1.79223e-05	0.00299346	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420386	TCAGCCTGACAGGAA[A/G]GGACAGTGCCCTGTG	80196
rs782225104	in-del	-/TT/TTT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404387	GGCTGTCATTTAATC[-/TT/TTT]TTTTTTTTTTTTTTT	80196
rs782235201	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421029	TTGGTTTTTCTTACT[A/G]TAATTAACTATTTGT	80196
rs782237373	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413871	TGAGCCACCGCGCCC[A/G]GCTTCACCTGACTTT	80196
rs782239539	snp	A/G	1.64779e-05	0.00287031	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417806	TTCTAGCTTTTTTAC[A/G]CGTTCGTTTTTTTCA	80196
rs782242124	snp	C/T	1.6473e-05	0.00286988	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417679	TGAGAAATATACCCA[C/T]AGATACTTGTCGTGA	80196
rs782242313	snp	A/C	1.70417e-05	0.002919	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417928	TACGAGGGGGTAACT[A/C]ATTACACCCAGGGCC	80196
rs782245420	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424722	TCTCAAAAAAAAAAA[A/G]AAAGAAAAAAAAGAA	80196
rs782246335	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408968	TTGTTAAAAACTCAG[A/G]TGACCCTTTCTTTTT	80196
rs782252587	snp	A/G	2.8014e-05	0.00374248	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423399	AGATGGCGAGCGGCT[A/G]CAGCTGCAGGATGAG	80196
rs782258361	in-del	-/AAAAAT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408448	CTCTGTCTAAAAAAT[-/AAAAAT]AAAAATAAAAATAAA	80196
rs782276767	in-del	-/TAAC			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403893	TGAATGACTGTGTAG[-/TAAC]TAACATATTAGAGTT	80196
rs782277096	snp	G/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399939	GCGCACTCCCAGCCA[G/T]GAGGAACGCCAGAGG	80196
rs782277334	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423534	TGAGTGTCCCATCTG[C/T]CGGCAGTATGTGGTG	80196
rs782279180	snp	C/T			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420270	TCACTTCAGCAAACA[C/T]AGAAGATGATGATGA	80196
rs782282024	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419380	TTACTCAGAACGTCT[C/T]CTAGTCGTCAAGCAA	80196
rs782287651	snp	C/G			intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402803	AAAACCCAAGCATGA[C/G]GAAGGTAACATTTGT	80196
rs782288414	snp	A/C	2.006e-05	0.00316695	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400191	TCCTGGTAGAGCCGG[A/C]CGAGCTGAGGCGGTC	80196
rs782292139	snp	C/G			intron-variant	RNF34	GRCh38.p7	12:121401220	TTGAACGTTTTCTGT[C/G]CGTTAGCCAAGAGGG	80196
rs782302427	snp	C/T	3.92519e-05	0.00442994	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420226	TGACCTAATCAGATA[C/T]GTTGTATAAGTGTAG	80196
rs782303457	snp	C/T	3.29462e-05	0.00405857	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417675	ATTCTGAGAAATATA[C/T]CCATAGATACTTGTC	80196
rs782303635	snp	A/G	1.65288e-05	0.00287474	intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402799	AACAAAAACCCAAGC[A/G]TGAGGAAGGTAACAT	80196
rs782304541	snp	C/G	4.95913e-05	0.00497928	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420536	AGTGGGGAGGGTCTG[C/G]ACTTATGGGACCAGG	80196
rs782305735	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405216	AGTATGGGAGAAACA[A/C]TGTCAGTCTCTGCTA	80196
rs782306563	snp	A/T	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416189	ATGTGGGCTTCGTGC[A/T]GTGGGCTGCTGAATG	80196
rs782308425	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421047	ATTAACTATTTGTTA[C/T]AACCCTAATTAAATT	80196
rs782314946	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420214	CAGATTGATTCCTGA[A/C]CTAATCAGATACGTT	80196
rs782316300	snp	A/G	3.29611e-05	0.00405949	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417812	CTTTTTTACACGTTC[A/G]TTTTTTTCAAACTAT	80196
rs782317245	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414049	GTAATAGCAGAAACA[C/G]CCATTATCCTTCTGT	80196
rs782319381	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121419303	TGTAGCAGGCTGTGC[C/T]ATCTAGGTTTGTGGA	80196
rs782319399	in-del	-/A			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398371	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAATT	80196
rs782322280	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121413136	TTCAAGCGATTCTCC[-/T]TGCCTCGGCCTTCCA	80196
rs782325933	snp	C/T			intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402521	AAGTAACTTTTTAAC[C/T]TTGCAGTAACATCCA	80196
rs782325994	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422458	CCTAGTGCCTTCTCC[A/G]TTGGCATATCTGCCA	80196
rs782326655	snp	C/G	1.64879e-05	0.00287118	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416147	AACTGTGGGATTTGT[C/G]TTCCTTTTTAGGCGG	80196
rs782338312	snp	A/C			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398794	TTTTCCAAAAAAAAC[A/C]TAGGACTATTATGGA	80196
rs782338601	snp	C/T	3.41361e-05	0.00413121	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423555	GTATGTGGTGCGAGC[C/T]GTGCACGTGTTCAAG	80196
rs782340715	in-del	-/CTCTTTAAATGGAGGAAATTGTTCATGTAGGAAAAGACCAGGA	1.66136e-05	0.00288211	frameshift-variant, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417898	AACATCCAGATCTGG[lengthTooLong]AGTGCCGGCACAGGT	80196
rs782340848	snp	A/G	0.000151023	0.00868843	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420287	GAAGATGATGATGAC[A/G]ACGATGATGAGGATG	80196
rs782352386	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412062	AGAACATTAACTTTA[C/T]TATTATTAATTTTTT	80196
rs782353997	snp	C/G	2.03163e-05	0.00318712	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400212	TGAGGCGGTCGCGGC[C/G]ATGAAGGTGAGGGGC	80196
rs782358887	snp	A/T			intron-variant	RNF34	GRCh38.p7	12:121401747	TTTTTAAACAAGTTC[A/T]TTGAAAACAGACGTG	80196
rs782360505	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410109	CGGTGAGCCAAGATC[A/G]TGCCATCGCACTCCA	80196
rs782361765	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121400277	ATCCTGCCAGGGCAC[C/T]TGAAGCGCCTCCTTT	80196
rs782364026	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402826	ACATTTGTATCTATA[A/G]CACATGTTATTGTAA	80196
rs782367588	snp	A/G	1.66335e-05	0.00288383	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416428	GGGTCAGCATTCTTG[A/G]TTGTAGGTTATTTTG	80196
rs782372317	snp	A/C			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399080	GTGTAGGAAAATCGG[A/C]TGGGCCCGGTGGCTA	80196
rs782378053	snp	A/T			intron-variant	RNF34	GRCh38.p7	12:121401569	TCTAGAAGTAGCTTT[A/T]TTTCCTGAAAACCAC	80196
rs782378708	snp	A/G	1.64738e-05	0.00286995	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417638	AATGCGACTGAAGGT[A/G]AAGGACCTGCGGCAG	80196
rs782380765	snp	A/G	1.65263e-05	0.00287452	intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402805	AACCCAAGCATGAGG[A/G]AGGTAACATTTGTAT	80196
rs782381492	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415558	GAGGTGGAGGTTGCA[A/G]TGAGCCGAGATTGCG	80196
rs782385808	snp	C/T	3.29549e-05	0.00405911	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417807	TCTAGCTTTTTTACA[C/T]GTTCGTTTTTTTCAA	80196
rs782391840	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422152	TAAGTACTTTGCGGC[A/G]TAGGATATAACATGG	80196
rs782392508	snp	C/T	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416296	AAACCCTGAGTTTTC[C/T]ACCTACCCACCAGCA	80196
rs782393122	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405082	CTTATTGGCTGGAAA[C/T]TGTCATTCCTACTCT	80196
rs782395750	snp	A/G			intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420970	GTGATGTTCATTATG[A/G]CTGCGAGACCACCAC	80196
rs782395778	snp	A/G	3.45507e-05	0.00415622	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417939	AACTAATTACACCCA[A/G]GGCCCGGCACGCTTA	80196
rs782397455	in-del	-/TGT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414672	AAAATACTTTCCTGT[-/TGT]TGTTGTTGTTGTTTT	80196
rs782399360	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422055	GAAATGGTTTTCTGG[C/T]AGTGAGGGGAGAAGT	80196
rs782401806	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409009	TGGAGTCTTGCTCGG[G/T]CACCCAGGCTGGAGT	80196
rs782402058	snp	A/T	3.29451e-05	0.00405851	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416274	CCGGTCCATTCAGAT[A/T]TACACCAAACCCTGA	80196
rs782402719	snp	C/T	1.64754e-05	0.00287009	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417801	CAGACTTCTAGCTTT[C/T]TTACACGTTCGTTTT	80196
rs782408381	snp	A/G	1.65034e-05	0.00287253	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402841	GCACATGTTATTGTA[A/G]TAATCGATCAGTTTG	80196
rs782409165	snp	C/G	1.70577e-05	0.00292037	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417501	ATGCTTTTCTTTCTT[C/G]AGCATGTTTGCTGTG	80196
rs782409830	snp	C/T			intron-variant	RNF34	GRCh38.p7	12:121400590	CGTGCCCTTTCCCGC[C/T]CCGAGTCCTTGAACT	80196
rs782410315	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410453	GAAGCAGGAGAATTG[C/G]TTGAACCCGGGAGGC	80196
rs782410446	snp	A/T	1.6504e-05	0.00287258	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402842	CACATGTTATTGTAA[A/T]AATCGATCAGTTTGG	80196
rs782413627	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412139	CAATCTTGGCTCACT[A/G]CAAACTCCGCCTCCT	80196
rs782425854	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406705	TGGGTAGGAAAGGGA[C/T]TAGACTATCAAGAAC	80196
rs782426715	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121404994	TTTCCTCTTGCTTTT[C/G]TTGACTGTAATGATG	80196
rs782436084	snp	C/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423749	AACATTGGTCCATGC[C/G]GTGAGCCTGTCTGCC	80196
rs782438126	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412453	TTCACCGTGTCAGCC[-/A]AGGATGGTCTTGATC	80196
rs782440713	snp	C/T	1.99471e-05	0.00315803	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400182	TGCTGAGTTTCCTGG[C/T]AGAGCCGGCCGAGCT	80196
rs782446452	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418887	AATTTTTGTATTTTT[A/G]GTAAAGATGGGGTTT	80196
rs782447197	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402053	GATTTCTGGGCAGAG[A/G]CTGATTCCTGATGTC	80196
rs782451567	snp	C/T	1.65468e-05	0.00287631	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402773	AAGGATCAAGTATAC[C/T]GTTAAAAGAAAACAA	80196
rs782451830	snp	C/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416229	GAACTGGAGCTGTCA[C/G]GGGCCAGCAGTCAGC	80196
rs782452243	snp	C/G/T	4.94306e-05	0.00497124	intron-variant, synonymous-codon, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416368	TTCATTTTCAGTCTT[C/G/T]AGAAAGAAGGTGAGT	80196
rs782453199	snp	C/T	1.71764e-05	0.00293051	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420820	TGTAGTATTTTTCCT[C/T]AGGCTTTTAAAAACT	80196
rs782455220	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416399	TGGATGAAATGTTAC[A/G]TAACAACACACATGG	80196
rs782456613	snp	C/T	1.82111e-05	0.00301749	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423462	TGCCGTCATCGACTG[C/T]GTCCTACTGGAGTGT	80196
rs782458947	snp	C/T	3.54089e-05	0.00420752	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417955	GGCCCGGCACGCTTA[C/T]TCTTGGCCGTATATG	80196
rs782463794	snp	C/T	1.64738e-05	0.00286995	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417612	GAGACAGCATTTCAG[C/T]GCCCTCAGTTAATGC	80196
rs782465912	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411538	AACTATCCCTGATAC[A/G]AAGGTCATAATCTCT	80196
rs782471050	snp	A/G	0.000172667	0.00928997	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415293	TTATACCCAATTACA[A/G]ATGCGAAAACAGAGG	80196
rs782472432	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412891	GCCAGCTATTTTTGT[A/C]TTTTTAGTAGAGACG	80196
rs782475094	in-del	-/TA	6.60797e-05	0.00574765	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402817	GGAAGGTAACATTTG[-/TA]TATCTATAGCACATG	80196
rs782478784	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411424	CTATTCCCTTTACCA[C/G]AGCTGTGTAGTTGAA	80196
rs782480505	in-del	-/GG	1.67273e-05	0.00289195	frameshift-variant, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423523	AGCGCATGAGTGAGT[-/GG]GTCCCATCTGCCGGC	80196
rs782484568	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422023	AGAGCTTTCAGAGGT[C/T]GTAGGCTGCTGGCTG	80196
rs782485225	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409571	TATCAGAATTACCCA[-/G]GGAGTTTTCAAAAAA	80196
rs782485681	snp	C/T	0.000543492	0.0164758	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417591	TCTACTTGTCACTTA[C/T]TACAAGAGACAGCAT	80196
rs782486109	snp	G/T	3.29478e-05	0.00405867	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417769	TGGACACAAGCAGTC[G/T]GAATTCTTCAAGGTC	80196
rs782487943	snp	C/T	1.87131e-05	0.00305879	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423456	CATGGATGCCGTCAT[C/T]GACTGTGTCCTACTG	80196
rs782488001	snp	C/G	3.29457e-05	0.00405854	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420647	TTGATGATGTGGAAG[C/G]AATGAGCGTGCGCCA	80196
rs782491327	snp	C/T	1.68151e-05	0.00289953	splice-donor-variant, intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417913	GAGTGCCGGCACAGG[C/T]ACGAGGGGGTAACTA	80196
rs782491533	snp	A/G	7.72648e-05	0.00621502	utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423610	GGACAGTCACCCCCA[A/G]ACTTGACCCCCAACA	80196
rs782494061	snp	C/T	3.88599e-05	0.00440777	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423379	TTAGCTCTCTGTTGC[C/T]TTTCAGATGGCGAGC	80196
rs782501176	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415069	CCATTACACTCCAGC[C/G]TGGGCAACAAGAGTG	80196
rs782502665	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411873	GCTAAACTTGTAAAA[C/T]TGCACTTCTGTTAAC	80196
rs782505600	snp	C/G	1.68755e-05	0.00290473	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423501	GGTTACCTGCACCAA[C/G]TGCGGCAAGCGCATG	80196
rs782509234	snp	C/G	2.01278e-05	0.0031723	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400196	GTAGAGCCGGCCGAG[C/G]TGAGGCGGTCGCGGC	80196
rs782510013	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410069	TGAGGCAGCAGAATC[A/G]GTTGAACCTGGGAGG	80196
rs782510647	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405231	CTGTCAGTCTCTGCT[A/G]TGGGAGGAAAAAGAG	80196
rs782512450	snp	C/T			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399858	CCGAGAAAGCAGCGC[C/T]GCAGCGCGCCTTCCG	80196
rs782512887	snp	G/T			intron-variant	RNF34	GRCh38.p7	12:121401105	GGTAATCTAGCAGGT[G/T]AGCTGCTAGATTAAC	80196
rs782521223	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421818	CAGACTAACAAATCT[C/T]ATGTTCCTATCTAGC	80196
rs782526012	snp	G/T			intron-variant	RNF34	GRCh38.p7	12:121401039	AAGGTGATGATAACT[G/T]TCAGACCTAGATGGT	80196
rs782526621	snp	A/G	0.000159087	0.00891729	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400172	GCTGCTATGGTGCTG[A/G]GTTTCCTGGTAGAGC	80196
rs782537938	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414686	GTTGTTGTTGTTGTT[G/T]TTTCGAGATGGACTC	80196
rs782545231	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420480	ACTTCTAGGACTGCT[A/G]AGATGGCTGGGAGAA	80196
rs782546188	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416244	GGGGCCAGCAGTCAG[C/T]ATTTGCAGGAGCCAC	80196
rs782547630	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RNF34	GRCh38.p7	12:121400102	CCGGACGCTCGGTCG[C/T]CTCCCGGGGCGCGGT	80196
rs782547969	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408965	GATTGTTAAAAACTC[-/A]AGGTGACCCTTTCTT	80196
rs782550295	snp	C/G	1.64732e-05	0.0028699	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420676	CAGCTGAAGGAAATT[C/G]TGGCTCGGAATTTTG	80196
rs782550390	snp	A/G			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121424470	GGTGCGGTGGCTCAC[A/G]CCTGTAATCCTAGGA	80196
rs782557827	snp	C/T	3.29468e-05	0.00405861	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417778	GCAGTCTGAATTCTT[C/T]AAGGTCCCAGACTTC	80196
rs782566488	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398611	TTATTAACTCTGGAG[A/G]TAGACCTGCCAGGCC	80196
rs782570149	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406530	GAGCTCAAGCAATCC[A/G]CCCACTTCAGCCTCC	80196
rs782574437	snp	C/T	1.67321e-05	0.00289236	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423531	GAGTGAGTGTCCCAT[C/T]TGCCGGCAGTATGTG	80196
rs782574942	snp	G/T	3.68738e-05	0.00429366	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423382	GCTCTCTGTTGCCTT[G/T]CAGATGGCGAGCGGC	80196
rs782575372	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420417	GACATTCGCTAGATT[A/G]GTACAGGATGTTTCT	80196
rs782583004	snp	A/G	4.723e-05	0.0048593	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420265	TGAAATCACTTCAGC[A/G]AACACAGAAGATGAT	80196
rs782588944	snp	A/G	5.98534e-05	0.0054702	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400183	GCTGAGTTTCCTGGT[A/G]GAGCCGGCCGAGCTG	80196
rs782591120	snp	C/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398523	TTACCCATCCTTGCA[C/G]GCGCACAGCGGTATC	80196
rs782594419	snp	A/G			intron-variant	RNF34	GRCh38.p7	12:121401132	TAACGCTGTCTCCAT[A/G]AAGCGTCAAAGATTT	80196
rs782596188	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421027	ATTTGGTTTTTCTTA[C/T]TATAATTAACTATTT	80196
rs782600448	snp	C/T	7.97162e-05	0.00631282	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420354	GGCCACCTATAAAAT[C/T]TGGTTTCCCTGACAT	80196
rs782602298	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121403975	CTTGCTATTTACCTA[C/G]TTTAATAAAAAGTGA	80196
rs782608817	in-del	-/TT/TTT			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415840	GACTTTTGTCCAGTC[-/TT/TTT]TTTTTTTTTTTTTTT	80196
rs782611921	snp	G/T			intron-variant, synonymous-codon	RNF34, KDM2B	GRCh38.p7	12:121408698	ATTTATCTTCTGGAT[G/T]GATTCTTCATCCTGG	80196
rs782614643	snp	A/C	1.64743e-05	0.00287	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417594	ACTTGTCACTTATTA[A/C]AAGAGACAGCATTTC	80196
rs782615108	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398842	TGAGCAGCACTTGAA[A/G]CAAGAGAAATACATA	80196
rs782619597	snp	C/T	1.65551e-05	0.00287702	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402756	GGTGGGGGAGTGGTA[C/T]TAAGGATCAAGTATA	80196
rs782620616	snp	C/T			intron-variant, utr-variant-3-prime	RNF34, KDM2B	GRCh38.p7	12:121402471	GGTTTGGTTTAGAAA[C/T]TGATGTTTTGAAATA	80196
rs782628145	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398647	TAATGAGGGACAACC[A/G]TGGCTTTGTACCCCA	80196
rs782630807	in-del	-/CT			upstream-variant-2KB	RNF34	GRCh38.p7	12:121398902	GGCCTGCCACGCACT[-/CT]CTCTCTCTCTCCGTG	80196
rs782631536	snp	C/T	1.65105e-05	0.00287315	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416130	GATTCCACTTAGCTT[C/T]AAACTGTGGGATTTG	80196
rs782635682	snp	A/G	1.6609e-05	0.0028817	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417897	CAAACATCCAGATCT[A/G]GAGTGCCGGCACAGG	80196
rs782642706	snp	G/T	1.64751e-05	0.00287007	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420609	GGAGAGAGTGAGAGC[G/T]TCACTGTCTGACTTG	80196
rs782643365	snp	C/T	0.000121421	0.00779074	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420233	ATCAGATACGTTGTA[C/T]AAGTGTAGGTACAAA	80196
rs782647439	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411883	TAAAACTGCACTTCT[C/G]TTAACCCTGGAATGA	80196
rs782648150	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421905	TGGTTATAATACAGC[A/G]TTTGTTGATGAACAG	80196
rs782648816	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416253	AGTCAGCATTTGCAG[A/G]AGCCACCGGTCCATT	80196
rs782649938	snp	G/T	1.65211e-05	0.00287407	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402815	TGAGGAAGGTAACAT[G/T]TGTATCTATAGCACA	80196
rs782650657	in-del	-/C	5.30124e-05	0.00514815	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423361	TGCCTGAAGCCGAGG[-/C]CCTTAGCTCTCTGTT	80196
rs782650665	snp	A/G			missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423391	TGCCTTTCAGATGGC[A/G]AGCGGCTGCAGCTGC	80196
rs782652346	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121424161	GGCCTTAGACTCCAC[A/G]TGTCCATTTTTGTTC	80196
rs782654219	snp	A/T			intron-variant, missense	RNF34, KDM2B	GRCh38.p7	12:121402800	ACAAAAACCCAAGCA[A/T]GAGGAAGGTAACATT	80196
rs782654843	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416879	GCCTCCTTGCTCTCT[C/T]TGATCTTTAGTTTAG	80196
rs782657826	in-del	-/TG			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410871	AATATGTGTCTGAGT[-/TG]TGTACTGAATATTGG	80196
rs782659625	snp	A/G	5.60994e-05	0.0052959	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423358	GCCATGCCTGAAGCC[A/G]AGGCCTTAGCTCTCT	80196
rs782660123	snp	A/C	1.65348e-05	0.00287526	intron-variant, utr-variant-5-prime	RNF34, KDM2B	GRCh38.p7	12:121402792	AAAAGAAAACAAAAA[A/C]CCAAGCATGAGGAAG	80196
rs782660604	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423155	AACATTTGTTGGGTA[C/T]GTCAAGCATTTTATT	80196
rs782662202	snp	A/G	1.64817e-05	0.00287064	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416159	TGTGTTCCTTTTTAG[A/G]CGGGTGCCACGTCTA	80196
rs782662795	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408272	ATGGTGAAACCCCGT[C/T]TCTACTAAAAATACA	80196
rs782662844	snp	C/G	6.58913e-05	0.00573945	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417663	CGGCAGTATCTCATT[C/G]TGAGAAATATACCCA	80196
rs782664752	snp	A/T	4.95029e-05	0.00497484	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416400	GGATGAAATGTTACA[A/T]AACAACACACATGGG	80196
rs782666196	snp	A/G	8.23649e-05	0.00641683	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417632	TCAGTTAATGCGACT[A/G]AAGGTGAAGGACCTG	80196
rs782668008	in-del	-/AC			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421382	CTCTAAAAAAAAAAA[-/AC]AAAAAAAAAAAAAAA	80196
rs782669486	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121416501	AGCTTAGTTCCATTA[C/G]CCATTTTCCATCTAG	80196
rs782675008	snp	C/T	1.8882e-05	0.00307256	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420215	AGATTGATTCCTGAC[C/T]TAATCAGATACGTTG	80196
rs782675815	snp	C/G/T	4.94208e-05	0.00497075	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420682	AAGGAAATTCTGGCT[C/G/T]GGAATTTTGTCAACT	80196
rs782675978	in-del	-/TTTA/TTTTA			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121415861	TTTTTTTTTTTTTTT[-/TTTA/TTTTA]ACATGCCTGTGTACA	80196
rs782676250	snp	A/C/G	1.73497e-05	0.00294527	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420333	AAAACGCAGAGGATC[A/C/G]GGTGAGGCCACCTAT	80196
rs782679258	snp	C/G	1.69934e-05	0.00291486	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423492	TGGGCACATGGTTAC[C/G]TGCACCAAGTGCGGC	80196
rs782681044	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121405015	TGTAATGATGTTTCA[C/T]GGGCTTATATTGTTT	80196
rs782682116	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411008	GGCGTAAGCATAGCT[C/T]ACCATAGTCTCAACC	80196
rs782683123	snp	C/G/T	1.6477e-05	0.00287024	intron-variant, synonymous-codon, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417803	GACTTCTAGCTTTTT[C/G/T]ACACGTTCGTTTTTT	80196
rs782683567	in-del	-/A	1.64838e-05	0.00287083	intron-variant, frameshift-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417553	CGTTTGTTCAGTCTT[-/A]ACAAGAAAATCTCCG	80196
rs782684013	in-del	-/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414499	CCCTGGTGGCTCAAA[-/G]GAGAGGGAAGAGACA	80196
rs782688135	in-del	-/T	3.29894e-05	0.00406123	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420565	GGCTAATGGATGCTC[-/T]TGTGGTTTCAGAACC	80196
rs782689740	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408867	CAAAGGCAAAGAGCA[A/G]ATAAAATCAAGGAGA	80196
rs782698389	snp	A/G	1.65053e-05	0.0028727	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121402852	TGTAATAATCGATCA[A/G]TTTGGCCAATGTCTT	80196
rs782698670	snp	A/G	1.64738e-05	0.00286995	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420683	AGGAAATTCTGGCTC[A/G]GAATTTTGTCAACTA	80196
rs782701935	snp	A/G			utr-variant-3-prime, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423990	CCACAAGTGGCCGAC[A/G]TGGAACATGCTGAGC	80196
rs782706106	snp	A/G	1.64732e-05	0.0028699	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416230	AACTGGAGCTGTCAG[A/G]GGCCAGCAGTCAGCA	80196
rs782707476	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121414385	TTTGGCCCTCGCTGA[A/G]AATTTATTCTTTTAT	80196
rs782708145	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412402	CCGCCACCACGCCAG[A/G]CTAATTTTGTTTTTG	80196
rs782712832	snp	C/T	3.50533e-05	0.00418634	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417947	ACACCCAGGGCCCGG[C/T]ACGCTTATTCTTGGC	80196
rs782712897	snp	A/C	0.000329551	0.0128323	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423422	AGGATGAGGAAGACG[A/C]CAGCCTGTGTCGCAT	80196
rs782716204	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121408057	ATGCCTGTAATCCCA[G/T]TGATTTGGGAGGCTG	80196
rs782717878	in-del	-/T	5.97699e-05	0.00546639	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400179	TGGTGCTGAGTTTCC[-/T]GGTAGAGCCGGCCGA	80196
rs782717990	snp	C/T	1.65999e-05	0.00288091	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417521	TGTTTGCTGTGACTG[C/T]AAGAAGGATTTTTGC	80196
rs782718487	snp	C/T	0.000206668	0.0101632	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420292	TGATGATGACGACGA[C/T]GATGAGGATGATGAT	80196
rs782719902	snp	A/T			intron-variant, downstream-variant-500B	RNF34, KDM2B	GRCh38.p7	12:121402127	TTCTGTGGAATTAAA[A/T]TTACATTAAAAGCTA	80196
rs782731813	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121407914	CCCCCCATCCCTTGT[A/C]CCCCTCTCCACTGTA	80196
rs782732941	snp	A/G	5.96819e-05	0.00546236	utr-variant-5-prime, nc-transcript-variant	RNF34	GRCh38.p7	12:121400173	CTGCTATGGTGCTGA[A/G]TTTCCTGGTAGAGCC	80196
rs782733770	snp	A/G	1.65151e-05	0.00287355	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417854	TGCTACTATGTCTTC[A/G]TTTCAGGGAGAGCTT	80196
rs782734327	snp	G/T	1.73099e-05	0.00294188	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121423565	CGAGCCGTGCACGTG[G/T]TCAAGTCCTGAAACA	80196
rs782735228	snp	A/C	1.64732e-05	0.0028699	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417698	TACTTGTCGTGAGAA[A/C]GAAGACTTGGTGGAT	80196
rs782736436	snp	C/T	1.64732e-05	0.0028699	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417720	TTGGTGGATCTAGTA[C/T]TGTGCCATCATGGAC	80196
rs782737126	snp	C/T	1.6495e-05	0.0028718	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121420565	GGGCTAATGGATGCT[C/T]TGTGGTTTCAGAACC	80196
rs782737185	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121422173	TATAACATGGTTGTT[A/G]TTATGACAGCATGGT	80196
rs782740391	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121421219	GTAGATTTCTGTGTA[A/G]GTCACAAAAAGCTGA	80196
rs782742672	snp	C/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409607	GGTGCCCAGGCTGCA[C/G]CACAGACCAGTGAAA	80196
rs782744096	snp	C/T	1.71252e-05	0.00292614	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420816	TCCCTGTAGTATTTT[C/T]CCTTAGGCTTTTAAA	80196
rs782745947	snp	C/G/T	5.27814e-05	0.00513696	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417951	CCAGGGCCCGGCACG[C/G/T]TTATTCTTGGCCGTA	80196
rs782751804	snp	C/T	2.18912e-05	0.00330834	intron-variant	RNF34	GRCh38.p7	12:121400265	CTCGCCAATCCTATC[C/T]TGCCAGGGCACCTGA	80196
rs782753057	in-del	-/GAT	3.70165e-05	0.00430196	cds-indel, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420298	GACGACGATGATGAG[-/GAT]GATGATGATGATGAA	80196
rs782756762	snp	C/T	0.000430092	0.0146581	intron-variant	RNF34, KDM2B	GRCh38.p7	12:121417963	ACGCTTATTCTTGGC[C/T]GTATATGGTGGGGCC	80196
rs782757591	snp	A/G	1.64784e-05	0.00287035	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417571	AAGAAAATCTCCGTA[A/G]ATGTTCTACTTGTCA	80196
rs782765678	snp	A/C			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121418463	TAAAGGCTTGTAATT[A/C]ATATTTACTTGTACG	80196
rs782766685	snp	C/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406562	AAAGTGCTAGGATTA[C/T]AGGCGTGAGCCACCG	80196
rs782769692	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121411167	ACCTGGCCTCAAACA[A/G]TCCTCCCACCTTGGC	80196
rs782771158	snp	A/T	1.68496e-05	0.0029025	intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420795	TAGGTTTATCTTTTC[A/T]TTTTTTCCCTGTAGT	80196
rs782771959	snp	A/G	1.66513e-05	0.00288537	missense, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420311	GAGGATGATGATGAT[A/G]AAGAAGAAAACGCAG	80196
rs782773518	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121412805	TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCTGGG	80196
rs782774085	snp	G/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121406086	GAGCCACCGTGCCCG[G/T]CCTGTCTTATTTCTT	80196
rs782776114	in-del	-/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409146	ACCATGCCCGGCTAA[-/T]TTTTTGTATTTTTAG	80196
rs782782316	snp	C/T	6.59413e-05	0.00574163	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121420582	GTGGTTTCAGAACCC[C/T]GGGCTCTCCAAGGAG	80196
rs782800076	snp	A/T	2.17026e-05	0.00329406	intron-variant	RNF34	GRCh38.p7	12:121400244	GGTGGAGCCGGACAG[A/T]CCCTCCTCGCCAATC	80196
rs782801022	snp	A/G			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121423330	TCGGACTGGGAGGGT[A/G]GCTGGCTGACTGGCC	80196
rs782803170	snp	A/C	3.29989e-05	0.00406182	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417830	TTTTTCAAACTATAC[A/C]GCCCCCTCTGCTACT	80196
rs782806965	snp	A/G	1.65627e-05	0.00287769	synonymous-codon, intron-variant, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121417887	GGATGGAGACCAAAC[A/G]TCCAGATCTGGAGTG	80196
rs782810265	snp	A/T			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121409540	AGCAGGTCTTAAGCT[A/T]TTAACCTGGCCTGTA	80196
rs782812909	snp	A/G			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399815	AGCAGCTTCCTCAGG[A/G]ACGCTATCTCCCATT	80196
rs782816324	snp	C/T	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416195	GCTTCGTGCTGTGGG[C/T]TGCTGAATGAAGTCA	80196
rs782820111	snp	A/T	1.6473e-05	0.00286988	intron-variant, missense, nc-transcript-variant	RNF34, KDM2B	GRCh38.p7	12:121416341	CAACATAGTTTGTAA[A/T]GCCTGTGGGCTTTCA	80196
rs796097661	in-del	-/C			upstream-variant-2KB	RNF34	GRCh38.p7	12:121399645	CCCCGAGGTCATCAC[-/C]GAGCATGAACGCGGG	80196
rs796983470	in-del	-/A			intron-variant	RNF34, KDM2B	GRCh38.p7	12:121410558	ACCAAAAAAAAAAAA[-/A]TGCTGGATGGGAAAA	80196
rs199870385	snp	G/T						:	GGTATTTTCATGTTT[G/T]AAAAGCCATGAAAAT	80196

Page 1 | 2