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

RNF128

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs368390485	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106736939	AACCTACTAGTGTTT[C/T]TATTGTGGCTGTTCA	79589
rs368464682	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106766833	AGGTTTTCTTCTAGG[A/G]TTTTTATGGTTTTAG	79589
rs368494859	snp	C/T	4.57159e-05	0.00478078	synonymous-codon	RNF128	GRCh38.p7	X:106791149	CTCCCATGAAGAGGA[C/T]AATCGCAGCGAGACC	79589
rs368523414	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106724023	CTCAACTGCCTATCA[C/T]ACAGTTCTACCTGGT	79589
rs368673263	snp	C/T	0.000251144	0.0112031	synonymous-codon	RNF128	GRCh38.p7	X:106795668	AACCTTTGAAGAAGA[C/T]GAAACTCCTAATCAA	79589
rs368716928	in-del	-/AAAG			intron-variant	RNF128	GRCh38.p7	X:106694429	TAATAATTGATTCAC[-/AAAG]AGAGTTAATGTCCGT	79589
rs368802194	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106791265	AAGGTTAACGAGTGC[A/C]CTGCAATCCATTGTA	79589
rs368803663	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106744304	ATATCACTATAGATC[C/T]CATGCAGAAACAGCT	79589
rs368821515	snp	C/G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106736452	TCTTACACATACATA[C/G/T]ACACCCCTCTTAGAG	79589
rs368829539	in-del	-/AATA			intron-variant	RNF128	GRCh38.p7	X:106784980	GACTTTTACCTGATA[-/AATA]TTTATTGATCCTCTC	79589
rs368852768	snp	A/G	6.83995e-05	0.00584765	missense	RNF128	GRCh38.p7	X:106773065	ATTTTTTTCGTTTCT[A/G]TGTCCTTTTTTATTA	79589
rs368861095	snp	C/G	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106743223	TGTTGCCAATGATAA[C/G]ATTTAAGTTTTTAAG	79589
rs368912696	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716646	AGCTAGGCAGCAAAC[C/T]AGATAGCCTGCCCTC	79589
rs368955217	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106770458	TCTTTTTACTCTTTT[A/T]TTTCCTCTAAACTTC	79589
rs369013611	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106759441	TGCTAGGTATATACC[C/G]AAAAGAAAGGAAATC	79589
rs369046996	in-del	-/GA			intron-variant	RNF128	GRCh38.p7	X:106704433	CGAGACTCTGTCTCA[-/GA]AAAAAAAAAAAAAAA	79589
rs369054303	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106766992	TTTCCCCATTTCTTG[C/T]TTTTGTCAGGTTTGT	79589
rs369054354	snp	C/T	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106704338	CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA	79589
rs369220463	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106717525	TTAATAGGGTTAACT[C/T]TTAATTTAACTTGTC	79589
rs369375431	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106767307	AATTACCTTGGGCAG[A/T]ATGGCCATTTTCACA	79589
rs369399897	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106758770	ATCTCCTGCCATATA[C/G]AAAAATCAAATCAAA	79589
rs369535012	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106704243	GATCAAAACCATCCT[A/G]GCTAATACGGTGAAA	79589
rs369541053	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106710148	CTGAACTATGAAAAA[A/C]ATAGATAATCTCAAT	79589
rs369547929	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106792172	AACTAGTTATAAGTA[C/T]CTTAATAATCTGTGG	79589
rs369567328	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106760095	AAAACTAAAAATTTT[A/C]TAAAAAGAATAAAAA	79589
rs369595554	snp	C/T	0.000241563	0.0109874	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795764	TAACAGAACTGCCAA[C/T]CAGGGCCTAGTTTCT	79589
rs369659290	in-del	-/G			intron-variant	RNF128	GRCh38.p7	X:106771656	GTACGGTCTGTCACG[-/G]CTTCCCTTTGCTAGG	79589
rs369678803	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106761320	AGGGAGCGCTTATAC[A/G]CTGCTCGTGGGAATG	79589
rs369794616	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106732291	CTTTTTGTTCCAATA[G/T]CACTTCCTCTCTTAT	79589
rs369798013	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106721457	TCTGCCACAATGGTT[C/T]CCTGCTGTTGCTCCT	79589
rs369836447	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106735892	CATTGTATCACTAGC[A/T]TTTTTTACCCTCCCC	79589
rs369840567	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106786910	ATGAAATACAACTAC[A/G]CATTCATTAGAATGG	79589
rs370041439	in-del	-/T/TT/TTT	0.254399	0.255354	intron-variant	RNF128	GRCh38.p7	X:106785049	GCTGTTTTTTTTTTT[-/T/TT/TTT]ACAGAGGCAATTAAA	79589
rs370042706	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106732880	TAAAATGCTTCCATT[A/G]AACATGTTGGTGAAT	79589
rs370066538	snp	A/C	0.00633741	0.0559334	intron-variant	RNF128	GRCh38.p7	X:106755375	ACTATTCTGAAAAAA[A/C]GGAGCAGGAAGAAAT	79589
rs370075392	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106704536	GGGCACGAACAGATG[A/G]GCTGCCTTACTGAAA	79589
rs370102440	snp	A/G	0.000189982	0.00974449	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727315	AGACAAGATCCATCT[A/G]GCTTATGAGAGAGGG	79589
rs370127729	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106750163	TCATCCCAATTCCAC[A/G]TTCACGTGGCTATGG	79589
rs370222953	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106773715	CAAATATTAATAGTT[G/T]CTACCATATTATAAC	79589
rs370231381	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106768605	TTTGATTCTTCTCTC[C/T]TTTCTTCTTTATTTG	79589
rs370328538	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106769546	TGCTACACCTGCTTT[G/T]TTTTTTTTTTTTTTT	79589
rs370426098	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106712034	TACAAATATGCTAAG[A/T]TTTGCCATTAATTTA	79589
rs370439617	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106722910	ATTTTAATGACTCAC[A/G]TTATCAAGCTATGGT	79589
rs370492938	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106792853	GTCTATCCAGCACCC[A/C]GCACATAGTAGATAC	79589
rs370518464	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106774993	TAAAAACTTCATAAA[G/T]ATTAGATACCAGCAT	79589
rs370608736	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106747407	TTCTTTGGGATGAGC[A/G]CTATGTTTGTTTAGA	79589
rs370671381	snp	C/T	0.00030709	0.0123875	intron-variant	RNF128	GRCh38.p7	X:106785032	TCTTTTAAAAAATAG[C/T]TTTTCTAATACCTGC	79589
rs370736559	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106768805	TCTTTTAATTGTGAT[A/G]TTAGGGTGTCAATTT	79589
rs370743721	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106763642	CTCCCGAGTAGCTGG[G/T]ACTACAGGCGCCCGC	79589
rs370777000	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106778663	AGCAGGATGCACCTA[C/G]TAAGCAGTCCCTTCA	79589
rs370856568	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774795	TTTCAGATGAAAATA[C/T]ATTTTTATATGTACT	79589
rs370860724	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106779668	TTCACCCTTTCTTCA[C/T]TGTTCTTCCTTATAG	79589
rs370922811	snp	A/G	0.00105904	0.0229869	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692610	GAACTGTTAATTCTC[A/G]CCTGCAGGGTCCACT	79589
rs370926653	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106694559	TGTAATTACTTTATT[A/G]TTATTTAATATTTTT	79589
rs370949109	snp	A/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106793670	TCTTTCATGACCTTG[A/T]CACTTCTGAAGATTA	79589
rs371009977	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106724450	ATTATATTACTCCTC[A/G]TTTTTGGATAAAGTC	79589
rs371011401	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746565	CCAGCAGGATCCTAC[A/G]GTGGATTTCTATACG	79589
rs371015713	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106705752	GCAAGATTAGCTGCA[A/G]TTGGAGGCCACAGTA	79589
rs371018455	in-del	-/GT			intron-variant	RNF128	GRCh38.p7	X:106710744	CCTGGACGAAAGTCT[-/GT]CAAAAAAAAAAAAAA	79589
rs371020089	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106722361	ATGCAGATCCCCTGG[A/G]GATCATGTTAAAAGA	79589
rs371045104	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106794190	CTATAGGATCCTAGA[C/T]GTTTCTTTCATTCTA	79589
rs371053898	in-del	-/T	0.233308	0.249442	intron-variant	RNF128	GRCh38.p7	X:106700029	AATTTATTTATTTAA[-/T]TTTTTTTTTTTGATA	79589
rs371096302	snp	A/G	0.000555846	0.0166618	intron-variant	RNF128	GRCh38.p7	X:106787864	CTGATCTTGTTCTGT[A/G]GTTTAATGTATTTTT	79589
rs371103952	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106762406	CCACAACCTCTGCCT[C/T]GGGTTCAAGCGATTC	79589
rs371182885	multinucleotide-polymorphism	AAA/GAG			intron-variant	RNF128	GRCh38.p7	X:106704232	CGAGGTCAGGAGATC[AAA/GAG]ACCATCCTAGCTAAT	79589
rs371230846	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106735874	CTTTCTCTTCTCTTT[A/G]CCCATTGTATCACTA	79589
rs371282965	snp	A/G/T	7.02302e-05	0.00592545	synonymous-codon	RNF128	GRCh38.p7	X:106694329	AAAAATTCAAACAGC[A/G/T]GGCAGAAGAAATGCT	79589
rs371283175	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106729357	TACTGAGCCTTGGAT[A/G]CCCCATCTGTAAGAT	79589
rs371328477	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106771102	AGATGTGGCTGCCTG[A/T]TCCTTCCTCTGGAAG	79589
rs371393322	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106705085	GAGAAGCATGTCAAT[A/G]TTTGGGCAGGGAGGT	79589
rs371417295	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106770014	TCACTTTTGAAGCTT[A/T]GTTTGGCTGGATATG	79589
rs371502158	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106741901	CTGTAGTAGATAGTG[C/T]AAAAGCAGGACATCT	79589
rs371528767	snp	C/T	0.0057231	0.0531864	intron-variant, missense	RNF128	GRCh38.p7	X:106726927	CCATGGGGCCGCCGC[C/T]TGGGGCCGGGGTCTC	79589
rs371598132	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106791838	TTTTAGGGAGTTCTG[C/T]TTTTCCCTATAAAGA	79589
rs371636020	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711190	TCCCCACCTACTCAC[C/T]GCCTAGCCCCATGGG	79589
rs371675793	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106772260	TAATAGGTAGTGAAT[A/G]GAAATGTGCATTTCT	79589
rs371724433	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106730838	AAGTGAATGAACCAA[A/G]CAGTTTAATTAATGA	79589
rs371841631	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106754453	TTTTGTAGCGACAGG[G/T]TCTCACCATATTGCC	79589
rs371959836	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106766283	CTAGATCCTTGAGGA[A/T]TCGCCACACTGTCTT	79589
rs371971816	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106767147	TTTGAAGTCAGGTAG[C/G]GTGATGCCTCCAGCT	79589
rs371984090	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106785446	ATAATTGCAGTGTCC[A/T]TATAAGAGGGAGAGA	79589
rs371986353	snp	A/G	0.000185179	0.00962056	intron-variant	RNF128	GRCh38.p7	X:106790304	ATTAATATGTTATTT[A/G]TATGAAGAATATATG	79589
rs371990974	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106752347	GCAGCACAGCATGGT[A/G]AGAGAGATTCCTTTT	79589
rs372147233	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106707453	TCCAGTCAATTACCA[A/G]TCAGTGGTATTGACA	79589
rs372220527	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796514	TGGTCATTGATCTTC[A/G]TTCATGAATTAGTCT	79589
rs372229752	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106700752	TTTTTGCATATATAC[G/T]TACAGAAAACACGTA	79589
rs372354474	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106766573	GTTGTTTGATTTTTT[A/C]TTGTAAATTTGTTCA	79589
rs372395931	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106766929	AGTTTCAGCTTTCTA[C/T]ATATGGCTAGCCAGT	79589
rs372431037	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740017	CAAATGCAATTTCCA[A/G]CCCAATCCCCATATT	79589
rs372480315	snp	A/C	0.000189982	0.00974448	intron-variant, missense	RNF128	GRCh38.p7	X:106727177	CCTGGTACCGCCCGA[A/C]GGGCCCGGGGCGCTT	79589
rs372570049	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106753547	CAGAGAGGGAACAAA[C/G]GAAGAGATCACAAAA	79589
rs372581583	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106703548	AGTACACAATACTAC[C/T]TCTCCAGTGAGCATA	79589
rs372585989	snp	A/C			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726243	GTAAGAAAGGGTAAC[A/C]GCGCGCTTTTCCTGC	79589
rs372607451	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106783659	CACACATGTATTAGT[C/T]GGGTTTGTGTTGCTG	79589
rs372616790	snp	A/G	7.16658e-05	0.00598563	intron-variant	RNF128	GRCh38.p7	X:106791259	ATACTAAAGGTTAAC[A/G]AGTGCCCTGCAATCC	79589
rs372634283	in-del	-/TTA			intron-variant	RNF128	GRCh38.p7	X:106704286	AAAAAATACAAAAAA[-/TTA]GCCAGGCGTGGTGGC	79589
rs372716238	in-del	-/GTGTGTGTGTGTGTGTGT			intron-variant	RNF128	GRCh38.p7	X:106779373	TGTGTGTGTGTGTGT[-/GTGTGTGTGTGTGTGTGT]TGAGGATACTTAAGA	79589
rs372722771	snp	A/G	0.0110639	0.0735497	intron-variant	RNF128	GRCh38.p7	X:106704290	AAATACAAAAAAGCC[A/G]GGCGTGGTGGCTGGC	79589
rs372846703	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106786331	TGAAGAAAGGATAGC[A/C]TTTTCAGGAGGATAG	79589
rs372889428	in-del	-/TTT			intron-variant	RNF128	GRCh38.p7	X:106704191	CTGTAATCCCAGCAC[-/TTT]GGGGGGCCAAGAAGG	79589
rs372892946	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106715319	CATTTAACATCTTTT[C/T]GCGTGCTTATTTTCC	79589
rs372905480	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106758951	AGATCACATCAAGCT[A/G]AAAAGCTTCTACCAG	79589
rs372924863	snp	A/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796177	AGCAATGCAAACTTA[A/G]GCGAGTACTTCTTGA	79589
rs372978875	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106730899	TATATAACACAGTTG[C/T]TTGTGTACATTGTTG	79589
rs373035444	in-del	-/ACTA			intron-variant	RNF128	GRCh38.p7	X:106707128	ATTCCTGAATTCCTA[-/ACTA]TTATAGACTAATAGA	79589
rs373074193	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106767985	AATCATGTGGTTTTT[A/G]TCTTTGGTTCTGTTT	79589
rs373106633	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106792782	CTTACTACACTGAGT[A/T]GTATTAAAACTTTTA	79589
rs373118337	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106720357	CACCAACACAATTTC[G/T]TTCTTTCTTATTTAA	79589
rs373134490	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106774274	ACTTCCACATCTTCT[C/T]ATCTATCTTCATCTG	79589
rs373149662	snp	C/G	0.000187977	0.00969293	intron-variant	RNF128	GRCh38.p7	X:106727405	TCACCCGGGTGAGTG[C/G]AGCTACTAGATTGCA	79589
rs373149711	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106733087	TACAGTATAACAACT[A/C]TTTACATAGCATTTA	79589
rs373186218	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106768755	TTTCTTGCCTTCTGC[C/T]AGCTTTTGAATGTGT	79589
rs373246565	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692168	TTGATGTTGAATTTA[C/T]CACAAAAGACTGTCC	79589
rs373258803	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106774326	TTGTCTTCTGTTTTT[A/G]TGGATGAACTGTTCC	79589
rs373259460	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106761010	TGGGAGAAAATATTT[A/G]CAAACTATGCATCCA	79589
rs373263175	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106741367	TTTAACTTGAGCTTT[C/G]GGCTAAAATGGCATG	79589
rs373298520	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106710264	AAAGCAGTGAAGATA[C/T]ACACAACAAAAGGCA	79589
rs373320786	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106732401	TTAATCTTTGTAATC[C/T]CTATAGAAACCTTTG	79589
rs373330951	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106735963	TTCTTTGTATTTTTG[G/T]TTTTTTTTCCCGTAA	79589
rs373435754	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106791442	TGAAATGCATCAGAG[C/T]GGGGATTATTTACAA	79589
rs373487234	snp	A/G	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106768412	GTTATTGGTCTATTC[A/G]GAGATTCAACTTCTT	79589
rs373519673	snp	A/G	0.0047581	0.0485429	intron-variant	RNF128	GRCh38.p7	X:106744759	CCACCAAGCCCAGCC[A/G]AATAAATAAATAAAT	79589
rs373584588	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106728427	TGAGAATGAATAATA[A/G]GAAAACTTATCCACA	79589
rs373627023	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106711433	CGACGGTTTTTTAAA[C/T]CTTCCTTTTGAAACT	79589
rs373677808	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106738685	TTAGGAATCAAATGG[A/C]TTTGGTATGAGTCCC	79589
rs373736767	snp	A/T	2.50272e-05	0.00353737	intron-variant	RNF128	GRCh38.p7	X:106785040	AAAATAGTTTTTCTA[A/T]TACCTGCTGTTTTTT	79589
rs373791741	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106773416	TTTAATTACATATAG[A/G]TGTAAATACATATGT	79589
rs373828059	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106751416	GGAGGAGAATTGTCC[A/G]TCCCTCTGGCAAGCC	79589
rs373863263	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106734423	AGGTAATGCCTTTTT[A/C]TTTTTCTTTTTTTAT	79589
rs373864013	snp	C/T			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795990	AAGAAGTCACGTTTT[C/T]CATTTATAACAATTT	79589
rs373865038	snp	A/G	2.28744e-05	0.00338182	synonymous-codon	RNF128	GRCh38.p7	X:106790234	GCTGTTAGAACACAG[A/G]ACTTGCCCCATGTGC	79589
rs373912729	in-del	-/CT			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693399	tctctctctctctct[-/CT]gtgtgtgtgtgtgtg	79589
rs373991994	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106765837	TAACTCGTCATTTAT[A/C]TTAGGTTTATCTCCT	79589
rs373992794	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106722197	TATACTTAAATTAAC[C/T]TCCCAACAAGAAAAG	79589
rs374004450	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106763806	GGGCCACCACGCCCG[A/G]CCAATTCAGGTTTTT	79589
rs374031219	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746429	AAGGTCCAGAGGCAC[A/G]GAACTTATTACATAG	79589
rs374100716	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106714412	TTTTTTAAAAATGTA[A/G]ATTTACATGCAGTTG	79589
rs374211264	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106701294	CTTTACTAAAAAGTG[C/T]TCCCACCGTTCTATC	79589
rs374223408	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106749918	TCAAAAAAAAAAAAA[-/A]GGAAATTAGGTATGC	79589
rs374255156	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106792008	AGATGACTTATGAAA[C/T]TTTCAGCTTCCTATT	79589
rs374274988	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106765455	ACTATTTTAATATTT[C/T]ACTGAGAAATGGCTT	79589
rs374275497	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765043	AAAATATAACAGAGG[A/G]TCTCTACATTTCAGA	79589
rs374318416	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106712695	TGAGTTAAAAGTTAA[G/T]TAAAAGGGTTATTTT	79589
rs374353627	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106723364	ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	79589
rs374385927	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106736372	TTCCTCTTAGAATGT[A/G]TTTTGTGTCATACTT	79589
rs374429077	snp	A/G	0.000361151	0.013433	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693998	TATACTCAAATGAAT[A/G]AGCAATGAACCAGGA	79589
rs374476933	snp	C/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106696943	TGCTTATGTGTTTTG[C/G]GGGAGAGTTGAAGGA	79589
rs374480205	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106764579	GGCTGAAGCAGGAGA[A/G]TCACTTGAACCCAGG	79589
rs374529846	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106742914	ATTGATATACATATA[A/T]GTATATGCACATATA	79589
rs374543950	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106793751	TCCGAGTGATTAAAT[G/T]TATTGTCCATTTTTG	79589
rs374544912	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722691	TGACTCACACTTAAC[C/T]AAATTCACGAGAGAC	79589
rs374546010	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106748739	CATGAAGATAGAGAG[A/T]AGATTGGTGGTTATC	79589
rs374553696	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106775354	AATAAATTTATTGAC[A/G]TGGCATTAAACCCCA	79589
rs374571146	snp	C/T	0.000967038	0.0219678	synonymous-codon	RNF128	GRCh38.p7	X:106787938	TGGCCCTGATGGAGA[C/T]AGTTGTGCTGTGTGC	79589
rs374577173	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106695178	AAGTAAACTTCTGAA[C/T]CCCATTTTGTTCACT	79589
rs374629704	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106770189	AACATTTTTTCCTTC[A/T]TTTCAACTTTGGTGA	79589
rs374649834	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106718663	CCCCATTAAAGTTCT[A/T]GTACTTTATACTGCA	79589
rs374755538	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106775520	AAGAATAGCATTAAA[A/T]CTTCTCATCTATTTG	79589
rs374818030	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106717163	AGCCGAGATCGCCTC[A/G]CTGCACTCAAGCCTG	79589
rs374932929	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106712471	GAGAAAGATCATTAG[A/C]GCTTTGATAAATCAC	79589
rs374933502	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106767300	ATCTATAAATTACCT[G/T]GGGCAGAATGGCCAT	79589
rs374964167	snp	A/G	0.0152462	0.0859689	intron-variant	RNF128	GRCh38.p7	X:106718180	CAAACATATGCTCTC[A/G]TCAGGTCTCTAAATA	79589
rs374988755	snp	G/T	0.0157677	0.0873799	intron-variant	RNF128	GRCh38.p7	X:106704302	GCCAGGCGTGGTGGC[G/T]GGCGCCTGTAGTCCC	79589
rs375024390	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106757667	TGCAGCGCACCAGCA[C/T]GGCACATGTATACAT	79589
rs375054299	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106753209	CCTTGAGTAGGAAGA[C/T]TAAGAGATGAACCTA	79589
rs375109476	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106773170	AAGCAGGTTTGTAAT[C/G]GTCCTTTCTTCCACT	79589
rs375128768	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106736525	ATTCCACTTCTTTTG[A/G]TGTAGTAGTAAACAT	79589
rs375223208	snp	A/G	7.14617e-05	0.0059771	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795750	TGAACCATTAGTAAT[A/G]ACAGAACTGCCAATC	79589
rs375240690	snp	A/C	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106768225	CAGGATGATGCTGGC[A/C]TCATAAAATGAGTTA	79589
rs375289835	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106712118	CTTTGATCACTCAAC[A/G]TACTTCAGAGTCACG	79589
rs375297842	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106703615	ATCATCATTGCCCTC[A/G]AGGAGGGAAATGTAG	79589
rs375378985	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106780053	AAGTACAGAAAAATC[C/T]AGTTTGCTTATATCT	79589
rs375407192	snp	C/T	2.29266e-05	0.00338567	synonymous-codon	RNF128	GRCh38.p7	X:106694296	GCTGATAGAAAGAGG[C/T]AATTGTACATTTTCA	79589
rs375413502	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106718783	GCTACCAACATAACC[A/G]TAACACTTGTCTAAT	79589
rs375534419	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106724530	ACCTCTCCAACATGA[C/T]CTGTTACCACCCTCC	79589
rs375594256	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106768978	TTTGTTATGTACCCA[G/T]TAGTCATTCAGGAGC	79589
rs375605611	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106749347	TTTGGAATTCGCTGG[C/T]GCATTATAAGAGACC	79589
rs375606491	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106723571	AAACTCTGTCTAAAA[A/T]ATATATATATATATG	79589
rs375630172	snp	C/T	0.00791544	0.0624105	intron-variant	RNF128	GRCh38.p7	X:106741538	TAAACCCAAGGTCTA[C/T]AGGATAGAATTAGTA	79589
rs375658024	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106729321	CAATAGCTTTGTGTC[A/C]TTGGTAGGATTATTT	79589
rs375709494	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106754830	TGAGTGCCTACATCA[A/G]AAATGTAGAAAACCT	79589
rs375750512	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106766962	TCCCAGCACCATTTA[G/T]TAAATAGGGAATCCT	79589
rs375809990	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106774829	CAGTTTCTCTAAAGG[C/T]GATCGATTTCTGGTC	79589
rs375825320	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106773512	AATTAGAAAGTACAC[A/G]GGAAAAAAACTCACC	79589
rs375830146	snp	C/G	0.000189982	0.00974449	intron-variant, missense	RNF128	GRCh38.p7	X:106727260	CCGTGCAAGTCTCTT[C/G]GTTGGCCCTCATCCA	79589
rs375900070	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106698210	TTGGAAGTTAAATAT[A/G]TTATTTTTAGGTAAA	79589
rs375904530	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106783760	TACAAGAAGCTTGGC[A/G]CCAACCTCCGCTTCT	79589
rs375994746	in-del	-/ATAA	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784977	ATTGACTTTTACCTG[-/ATAA]ATATTTATTGATCCT	79589
rs376155442	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106709800	ATCCCACCACCTCGG[C/T]CTCCCAAAGTGCTGG	79589
rs376171674	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106739102	CAATTTCTCTCTTCT[A/C]TTCTCTTCTCTTCTC	79589
rs376209535	snp	G/T	0.00499562	0.0497278	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106726931	GGGGCCGCCGCCTGG[G/T]GCCGGGGTCTCCTGC	79589
rs376290873	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106768444	CTGGTTTAGTCTTGG[A/G]AGGGTGTATGTGTCG	79589
rs376302276	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106743898	GAAAATGTGGCACAT[A/T]TACACCATGGAATAC	79589
rs376412008	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106711056	TTGAAAAATATTTTG[A/T]TCCACAGCAAATATA	79589
rs376418180	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106777952	TCCAGCCTGGGTGAC[A/T]GTGAGACCCTGTCTT	79589
rs376435759	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106761312	TAGAGAAAAGGGAGC[A/G]CTTATACACTGCTCG	79589
rs376450562	snp	A/G	9.43797e-05	0.00686884	synonymous-codon	RNF128	GRCh38.p7	X:106787935	AATTGGCCCTGATGG[A/G]GATAGTTGTGCTGTG	79589
rs376454194	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106743915	ACACCATGGAATACT[A/G]TGCAGCCATAAAACA	79589
rs376478820	snp	A/G			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692230	ACATTTATAATAACA[A/G]TAATAACATTTCTGT	79589
rs376505328	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791817	AATTTTATGCCAAAT[C/G]AGAAATTTTAGGGAG	79589
rs376568120	snp	G/T	0.000326569	0.0127741	missense	RNF128	GRCh38.p7	X:106791082	TGGATGTTGAAGATG[G/T]ATCAGTGTCTTTACA	79589
rs376569515	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106782607	TATTTTACTTTTTCA[A/G]CCCTCCACTTGAGCA	79589
rs376573582	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106774394	ATTTTTGTCTTTTGT[A/G]TACTCAAGGACATCA	79589
rs376663928	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106717112	GGAGGCTGAGGCAGG[A/G]GAATGGCGTGGACCC	79589
rs376667242	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106731990	ATTTTGGACTACATT[G/T]ATCAGCATGGCATAT	79589
rs376760842	snp	C/T			intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106726988	GCTGGCATGGTGCTT[C/T]CTGCTGGCCCTGAGT	79589
rs376813425	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106746928	TCTGTAACTACTATA[C/T]ACATTTGTTGTATCA	79589
rs376858780	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106768551	GTATTTCTGTGGGAT[C/T]GGTGGTGATATCCCC	79589
rs377016080	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106701454	ATATGTTTGTGTGTC[A/G]ATAGATACAGATAGA	79589
rs377024529	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711594	TTTTGTTCCAACCTT[A/G]TAAAAGAAAGGCCCA	79589
rs377067941	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106704891	GCAAGTATGGTACTT[A/G]GTTTATCAATGTAAA	79589
rs377180667	snp	C/T	0.000219874	0.0104828	intron-variant	RNF128	GRCh38.p7	X:106773202	TTAAAAAAAATTTAC[C/T]GTTCTAATTGTAGTT	79589
rs377215738	snp	A/C	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106720311	GCAATCAAGTGCATA[A/C]AATTTAGCTCAAGTT	79589
rs377253287	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106754748	GAAACAAGTGGAAAT[G/T]AAAACAAAATGTAAC	79589
rs377255350	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106704024	AAATGATAATGTCTT[C/T]GATAAATGTGTGAAA	79589
rs377265213	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106759787	CAGAGGCTGGGAAGG[A/G]TAGAGGTGGGTAGAA	79589
rs377271840	snp	C/T	0.000114098	0.00755221	synonymous-codon	RNF128	GRCh38.p7	X:106795650	TCCTCATGTTGACAA[C/T]CCAACCTTTGAAGAA	79589
rs377362745	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106793288	CACCTGGAGAGATTT[C/T]AAACTTTGCTGATGT	79589
rs377462229	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106735977	GTTTTTTTTTCCCGT[A/G]AGAGGCCTGCTTACC	79589
rs377524911	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106747131	ATATAAGATTTATGA[A/G]TAAATCCTTGATTGA	79589
rs377551899	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106768781	TGTGTTTGCTCTTGC[C/T]TCTCTAGTTCTTTTA	79589
rs377552030	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106723104	TATAAATTCACAATT[G/T]TAAACTCATTATTAC	79589
rs377608400	snp	A/G	0.0068637	0.0581785	intron-variant	RNF128	GRCh38.p7	X:106777049	ATAAATATTTCTGTG[A/G]CATTTCCGGATTTTT	79589
rs377610410	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106705731	TGCTCAGTTAACTTA[C/T]GTATAGCAAGATTAG	79589
rs377612644	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746510	TAGACAAAAACCATA[A/G]TATCATTAGCTTTTT	79589
rs377743326	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106762245	TGTACACATTGGCCA[A/G]CCTCTCTCCATCCTT	79589
rs386826792	multinucleotide-polymorphism	AA/GC			intron-variant	RNF128	GRCh38.p7	X:106704205	CTTTGGGGGGCCAAG[AA/GC]GGGCAGATCACGAGG	79589
rs386826793	multinucleotide-polymorphism	CG/TA			intron-variant	RNF128	GRCh38.p7	X:106704242	AGATCAAAACCATCC[CG/TA]GCTAATACGGTGAAA	79589
rs386826794	multinucleotide-polymorphism	GT/TA			intron-variant	RNF128	GRCh38.p7	X:106704590	CTCATGATAAGACGG[GT/TA]TTTGGTTGAGTCAGG	79589
rs386826795	multinucleotide-polymorphism	CT/TG			intron-variant	RNF128	GRCh38.p7	X:106753700	CAACTAGCTGCCATC[CT/TG]TAAGAAACACACTTC	79589
rs397968795	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106780378	AATCAAGAAAAAAAA[-/A]CCATGTAGTGGAGAT	79589
rs527600760	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772739	AACCAAATCTCATGC[A/G]TGTTTATATAACCTA	79589
rs528571308	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106696448	CTAGATGACCAGACA[C/T]TAGATCATTAAAGAC	79589
rs528611524	snp	C/T	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106731669	TCCTTGCCTCTCTTT[C/T]GTTTCATTACTATTT	79589
rs528655963	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106769584	TCCATTTGCTTGGTA[G/T]ATCTTCCTCCATCCC	79589
rs529249317	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106764245	GCTGGAATTACAGGC[A/G]TGAGCCACCACGCCC	79589
rs530313065	in-del	-/AATAT			intron-variant	RNF128	GRCh38.p7	X:106795386	AAGCAATTATAAATC[-/AATAT]AATAATGCCATATGT	79589
rs531012747	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106729133	TTACTTCTGTTAAGG[G/T]TATTTATCTGATAGT	79589
rs531939223	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751438	TGGCAAGCCTCACCA[C/T]TGTGAGCTAAAGTGC	79589
rs531948698	snp	A/G	0.00581083	0.0535878	intron-variant	RNF128	GRCh38.p7	X:106739055	TAACATCCGAAATAC[A/G]ATTTGGGTAGCACTG	79589
rs532551755	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772647	CTGTTGAATTATAGA[C/T]AGTTAATCTGAGGAG	79589
rs533083823	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696850	TACTTGTTGCAGCAA[C/T]TGGAAGAGCACACAC	79589
rs533493802	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763538	TTGAGACGGAGTCTC[A/G]CTCTGTCGTCCAGGC	79589
rs533694711	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106757903	GATATATCCACTTTT[A/G]CCACTGTTATGCAAC	79589
rs534283383	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106734306	ACTAGCCTTAAACAT[A/G]GTCTGATCTAACCCA	79589
rs534442699	snp	C/G	0.0261392	0.111294	intron-variant	RNF128	GRCh38.p7	X:106757970	GAGAAAGAAGGGCAA[C/G]AAAATTGGAAAGGAA	79589
rs534448541	in-del	-/GTAA			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796486	CTAATGACAGAGTAA[-/GTAA]CACTAATATTGGTCA	79589
rs535114910	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693147	TGTTAAAAATTAAAC[A/C]TTCAACAACCTTTTT	79589
rs535457790	in-del	-/TT			intron-variant	RNF128	GRCh38.p7	X:106719240	GGCATTTTTTTTTTT[-/TT]GAAACAGAGTCTCTG	79589
rs537199923	snp	C/T	0.0110639	0.0735497	intron-variant	RNF128	GRCh38.p7	X:106703665	GCAAGTCATAAAAGG[C/T]AGACTAGAAATGTTA	79589
rs537321004	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106792864	ACCCAGCACATAGTA[G/T]ATACTCAAATTTATG	79589
rs537336323	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106746246	GTTAATATTAGAAAA[C/T]GTTAGTTGAAAGAGA	79589
rs537373316	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106786276	AAACCCATATATATA[G/T]GGTCAGTTGATTTTC	79589
rs537775420	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106753854	TATAAAAAGAGATAA[A/T]GAAGGTCATTATATA	79589
rs538360204	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722774	TCCAAGTGGACCAGA[A/T]ACTAGTGTTTGCTAA	79589
rs538998444	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106738168	TTGAGTCAGACAGCT[A/T]GATTTGAATTCCAGC	79589
rs539770337	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106695889	CCTGTTTTCAAAACT[C/T]TCTTTGCAACCTGTA	79589
rs539794937	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106745404	TAATCTGTACTAATG[C/T]CTATTCTGCAACAGA	79589
rs540314909	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106724605	TAGTAATTGTAGCTT[A/C]CTAACATTTCTTTTT	79589
rs541107148	snp	C/G	0.0068637	0.0581785	intron-variant	RNF128	GRCh38.p7	X:106714157	CACTCCAGCCTGGGC[C/G]ACAGAGTGAGACTCC	79589
rs541702869	in-del	-/AC			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693364	GCCTGCTAAGAAAAC[-/AC]ACACACACACACACA	79589
rs541855621	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106766587	TCTTGTAAATTTGTT[A/C]AAGTTCATTGTAGAT	79589
rs543114219	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106794123	AACTTCTAATATAAG[A/G]AAGAGCTCTTCCTTC	79589
rs543252259	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106700493	AGCTACAAAACAATT[A/C]TCTTTTATATGTGAA	79589
rs543289546	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106766987	AATCCTTTCCCCATT[G/T]CTTGTTTTTGTCAGG	79589
rs543564120	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106770721	TTCAGAGAAGTTTGT[G/T]ATTACCGATCATCTG	79589
rs544557510	snp	G/T	0.0147244	0.0845304	intron-variant	RNF128	GRCh38.p7	X:106760026	ACAGATTGTATGTCT[G/T]TATCAAAATATCTCA	79589
rs545298487	snp	G/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725215	ACCATCAGTATTTGG[G/T]GGTACCATGCTATTG	79589
rs545311603	snp	C/G	0.0256233	0.11025	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725762	GAGGAAACTGAGCCA[C/G]AGGGAAGTTCCCCAA	79589
rs545432689	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106749071	ATGATATTTTAATCT[A/G]TCTTTGAAAAAAATG	79589
rs545468818	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106759211	TTGATCATCAGAAAT[A/G]CAAATAAAAACTACA	79589
rs546321893	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730860	AATTAATGATTTGGG[C/G]GTCTCCAATGGGATA	79589
rs546792011	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106771403	GTGGTGGGCTCCACC[A/C]AGTTTGAGCTTGCCC	79589
rs547047980	snp	A/G	0.00633741	0.0559334	intron-variant	RNF128	GRCh38.p7	X:106732704	TGCTGGCTAACTTCT[A/G]TGGTGATTAGCCTGG	79589
rs547277682	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720047	CTTTTGGAATCTTCA[C/T]CTTACTGGAAACCTG	79589
rs547293125	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106783611	TAGAAAGATCACTTA[C/T]CTTGCCATGCTGCAC	79589
rs548836215	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106751720	GCAGAGTCCTGAAGC[C/G]CACACTCCAGGCCCT	79589
rs548986093	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711830	GCAACTGCTTCAATT[A/G]TGAGAACACCAAGAC	79589
rs549212009	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106730372	GCAATCTCTGGATAT[A/T]TTTCAATCAAATCAG	79589
rs549233521	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791973	TTCTAGTATAAAAGT[A/C]AAACAAAAACTGATT	79589
rs549638729	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106697717	TACAGCCTCCCTACT[A/T]AGAGTGTTATTTTTC	79589
rs550234417	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106753673	AGAATGGCTGAATGC[A/G]TTAAAAAGCCCCAAC	79589
rs550271161	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106763752	ATCTCATGATCCGCC[C/T]GCCTCCTCGGCCTCC	79589
rs551037941	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106774802	TGAAAATACATTTTT[A/G]TATGTACTGAGCAGT	79589
rs551707349	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106739949	TGGATTTTGTGGCCA[G/T]GTCAAAATGAATACC	79589
rs552999941	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106758463	AAACCACAGAAGACC[C/T]AGAATAGCCAAAGCC	79589
rs553131973	snp	C/T	0.0026455	0.0362733	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693502	GGATCTTAACTTACT[C/T]CAGGCTGAACTGGTT	79589
rs553355084	snp	C/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106715100	GTTGGATGTTAGTTT[C/T]ATAAGAAACTGCCAG	79589
rs555059974	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767154	TCAGGTAGGGTGATG[C/T]CTCCAGCTTTGTTCT	79589
rs555140182	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106733927	GCTGGTCTCTAACGC[C/T]TGACCTCAAGTTATC	79589
rs555309003	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751943	TCCCAGCTGTAGTGG[C/T]CAAGGGGAGAGACTC	79589
rs555538101	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106706246	AGAGCAAGTTCTGGC[C/T]GACAATTGGATTTTC	79589
rs556183518	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106765910	TGTGTGATGTTCCCC[A/G]CCCTGTGTCCAAGTG	79589
rs556993387	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106705903	AGGACTCCTTGGAGC[A/C]GAACTCAGAGAGAGG	79589
rs557783780	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106694826	AACAGTTTCATTATG[C/T]TTAAATAATAGCATA	79589
rs558053889	snp	C/G	0.0100156	0.0700533	intron-variant	RNF128	GRCh38.p7	X:106696758	CAATGTTGTGTCTCT[C/G]TGCTTCTTTCTAATG	79589
rs559115671	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106718617	ATGCATCTGGGCTTT[C/T]TTTTCCTTTTGATGT	79589
rs559335986	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106716929	TATATATTGCCGGTC[A/G]CGGTGGCTCATGCTT	79589
rs559739479	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106738810	ATAGGGTTATTGTGA[G/T]GTGTAAATTAAATAA	79589
rs560091339	in-del	-/GTGT			intron-variant	RNF128	GRCh38.p7	X:106779352	TACACAGTTACGTGT[-/GTGT]GTGTGTGTGTGTGTG	79589
rs560776140	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106730539	GATTGTCACGAGACA[C/T]GTTAAGCATGTTCTC	79589
rs561349844	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106767104	ACCAGTACCATGCTA[G/T]TTTGGTTACTGTAGC	79589
rs561523339	snp	C/T	0.00581083	0.0535878	intron-variant	RNF128	GRCh38.p7	X:106730746	TCATAATTCATGAAA[C/T]ATTTACAACGTTATG	79589
rs562011609	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106719241	GCATTTTTTTTTTTT[-/T]GAAACAGAGTCTCTG	79589
rs562127240	snp	A/C	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106751317	TTTGCATCAGAACTC[A/C]GTGCTACCCTGTCAC	79589
rs562941593	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761052	ATATCCGAAATCTTT[A/G]AGGAACTTAAATTAA	79589
rs563599285	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106727407	ACCCGGGTGAGTGCA[G/T]CTACTAGATTGCACC	79589
rs564920137	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796568	ATTAGTCTGTTGAAA[A/G]TGTTTTCCAAACAAT	79589
rs565337949	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771644	CCGATTTTCCAGGTA[C/T]GGTCTGTCACGGCTT	79589
rs567606416	snp	A/C/G	0.00158814	0.0281345	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692180	TTATCACAAAAGACT[A/C/G]TCCATCAGCAATCTC	79589
rs568172903	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106755310	CCCAATGACTTCACT[A/G]CTGATTTTTGCCAAA	79589
rs568391745	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106764652	ACTCTGGGTAAGGAG[C/T]GAAACTCCGTCTCAA	79589
rs569262530	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777671	CTTCATGATAATCCA[C/T]GGCCTCTTAATTAAG	79589
rs569729896	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106785518	GAAGCAAGAGGGTGG[G/T]GTGATACAAGAAAGA	79589
rs569771669	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106773509	AGAAATTAGAAAGTA[C/T]ACGGGAAAAAAACTC	79589
rs570014951	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741816	TAGATACAGTGATGA[A/T]AGACCTAGTCCCTAA	79589
rs571571413	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106736244	TAAATTGAGTTACTT[C/G]TTTTTAAAATGAGCA	79589
rs571599825	snp	A/T			utr-variant-5-prime	RNF128	GRCh38.p7	X:106693934	CAGCAGGGACGTGAG[A/T]GGACAATGGTGACTG	79589
rs573318081	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106701598	AAGAAGAAACAATAG[C/G]TAAAAGGGACAATTT	79589
rs573697635	snp	C/T	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106710359	ATTATGGATAATACA[C/T]TAGGAAACTCAGAGA	79589
rs573759904	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106754166	TTGTCTCTTTGGCAC[A/G]TGGATCATTCTCAAG	79589
rs574485871	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106738458	TAGAAGCAGAAAAAA[C/T]GGAACATCCATATTG	79589
rs575271656	snp	C/G/T	0.000194826	0.00986805	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727183	ACCGCCCGACGGGCC[C/G/T]GGGGCGCTTAACGCC	79589
rs575572559	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106761351	TAAATTAGTTCAGCC[A/G]TTGTGGAAAGCAGTT	79589
rs575950236	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106765918	GTTCCCCACCCTGTG[C/T]CCAAGTGTTCTCATT	79589
rs576317400	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106697046	AAACCAGGAAATTCC[C/T]GGGAAAATTGTGACA	79589
rs576434545	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106748755	AGATTGGTGGTTATC[A/G]GAGGCCAGGAAGGGG	79589
rs576561499	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106759187	TATATGAAAAGATGC[G/T]CAACATAATTGATCA	79589
rs577229456	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106759774	GAAGGATGGTTACCA[G/T]AGGCTGGGAAGGGTA	79589
rs577539329	snp	G/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106721661	AATGGTCACAGTGCC[G/T]GAAATGCATACAAGA	79589
rs578222209	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106779955	AAGAATCCTCTTACT[A/G]TAATTCTTGATTTTA	79589
rs745358500	snp	A/G			downstream-variant-500B	RNF128	GRCh38.p7	X:106797298	ACTGAGTGAGAACTC[A/G]CTTATCACCAAGGGG	79589
rs745361413	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106720455	CTGGGCTCAAGCAAC[A/T]CTCCTGCCTCAGCCT	79589
rs745362482	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106701477	CAGATAGAGTCACCA[C/T]GTAGGATATGCCCAA	79589
rs745378500	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785211	AGGCTAAATGTTCTT[C/T]CTAAGTATGCTTTTA	79589
rs745399693	in-del	-/G			intron-variant	RNF128	GRCh38.p7	X:106712077	GGCTAGCCCACCGGT[-/G]GGTGGTTAAATCTCA	79589
rs745400434	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106749194	AACACACTGAAAATC[A/G]GGAGATTAAATATCT	79589
rs745407388	snp	G/T	5.04757e-05	0.00502348	splice-donor-variant	RNF128	GRCh38.p7	X:106694409	AGATGGCAAATTTTG[G/T]TAAGTAATAATTGAT	79589
rs745412738	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106703405	AGTGTCAGTATCTCC[A/G]TTTTATATATAAGAA	79589
rs745413317	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106774112	GGGCCCTTAATGCTA[C/T]CCAGGAATCACACTA	79589
rs745416928	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784500	CTTCATTAAGCAATC[A/G]TGGTTATAAGCACCA	79589
rs745422571	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796657	ACTAAAATTCTGTCC[A/G]TGTAACTATAAATTT	79589
rs745465290	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106750684	ACTCTTTCTGTAGAA[C/G]CAAGCTTGATTGTCT	79589
rs745477696	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106705114	GTAGGGTACGGTGGA[C/G]GGTAACAAGTGCTAA	79589
rs745516969	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728383	AACTTATTTCAAGTC[C/T]TAGAGTCTGGGTTCT	79589
rs745537838	snp	C/T	2.29505e-05	0.00338744	missense	RNF128	GRCh38.p7	X:106694300	ATAGAAAGAGGTAAT[C/T]GTACATTTTCAGAAA	79589
rs745545719	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106773571	GTCATCGCCCAAAGG[C/T]AACCACTATTATTTT	79589
rs745556949	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739252	TCAACCTCTACATCC[C/T]GGGTTCAAGCGATTC	79589
rs745561050	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106750785	AGAAGCAACAACTGA[A/C]GTGAGAACCTTCCTC	79589
rs745626032	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106707422	TTTTAAGTTGTCTTC[C/T]ATTTACTTTATATCA	79589
rs745629688	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106778329	ATAAATACTGTACAA[A/G]CAGTTACTGTACTGA	79589
rs745632417	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106761043	AAAGGTCTGATATCC[A/G]AAATCTTTAAGGAAC	79589
rs745647502	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768682	TCCTGGATTCATTGA[-/T]TTTTTTGAAGGGTTT	79589
rs745683070	in-del	-/AC			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796859	TTAGGCAAAAATAAA[-/AC]AGACATGTATTTTTG	79589
rs745685062	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106732956	GAGTCAGCCCCCTAT[A/G]TCTATGTCCACATCT	79589
rs745739526	snp	C/G	2.29637e-05	0.00338841	missense	RNF128	GRCh38.p7	X:106773144	TACGGAATGCAAGAG[C/G]TCAAAGCAGGAAGCA	79589
rs745740600	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106738802	TCTATGTCATAGGGT[C/T]ATTGTGAGGTGTAAA	79589
rs745789721	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106698033	AAAGGATATGTTTAC[A/C]ATGTTCTTAAGTAAG	79589
rs745793086	in-del	-/GAA	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106722153	AGAGGAGGGTGGAAG[-/GAA]GAAGAAGGACTGAAA	79589
rs745850379	in-del	-/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106733570	CTGTACATAGGCATA[-/T]ACTTTGTATTCTACT	79589
rs745851620	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106769362	CTAAGTCTCTTTGTA[G/T]GTCTCTAAGGACTTG	79589
rs745878720	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761547	TGCCCATCAATGGTG[A/G]ACTGAATAAAGAAAA	79589
rs745899251	snp	C/G	2.29938e-05	0.00339063	intron-variant, missense	RNF128	GRCh38.p7	X:106727335	ATGAGAGAGGGGCGT[C/G]TGGAGCCGTCATCTT	79589
rs745914582	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106770797	TGTTCTGTTGCTGGC[A/G]AGGAGCTGCATTCCT	79589
rs745940581	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106724484	ACTCCCTAGCTTTAC[C/T]CAAAGGACTCTCAAG	79589
rs745955923	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106746010	ATTTAGAAGTCCACT[C/T]GAATTGGTTCCAGAT	79589
rs745968964	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747446	ATGAAATTAATAAAT[G/T]ATTTGGAGAGATTCT	79589
rs745979005	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106778920	AAATTATCTGGAAGA[C/T]TCATTAAGTACCTGC	79589
rs745984646	in-del	-/AGAC			intron-variant	RNF128	GRCh38.p7	X:106753257	AAGTTTTGAAGACAT[-/AGAC]AGTATAATAAGATAT	79589
rs745995827	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106699381	ATAAGCGCAAGCTTT[C/T]GTACTTGCTGCCTCC	79589
rs745997623	snp	C/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725875	ATATAATAGTTGACA[C/G]GGTAGACAAAAATTG	79589
rs745998121	snp	A/G	2.87989e-05	0.00379455	intron-variant, missense	RNF128	GRCh38.p7	X:106727175	GTCCTGGTACCGCCC[A/G]ACGGGCCCGGGGCGC	79589
rs745999647	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710267	GCAGTGAAGATATAC[A/G]CAACAAAAGGCAAAT	79589
rs746006393	snp	C/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106752346	GGCAGCACAGCATGG[C/T]GAGAGAGATTCCTTT	79589
rs746050640	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106708618	CTTTTAAGTAGTATA[C/T]AGAAGCAACTGTTTT	79589
rs746055206	snp	C/T	2.28537e-05	0.00338029	synonymous-codon	RNF128	GRCh38.p7	X:106795677	AGAAGACGAAACTCC[C/T]AATCAAGAGACTGCT	79589
rs746081167	in-del	-/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725075	TGGCTGTCATTCAGG[-/T]TAATATCAATTGAAT	79589
rs746083215	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714883	TGCACATATTAATAG[C/T]TCCTTTCTTTCTATT	79589
rs746108405	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711322	TTAGTTGGTTTACAT[A/G]TTTATGGAGCAATCA	79589
rs746118783	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786496	AAACCTAGAACTATG[A/G]AATTTTTAGAACAAA	79589
rs746119417	in-del	-/TTTGA/TTTGGT			intron-variant	RNF128	GRCh38.p7	X:106763962	TTTGGTTTGGTTTGG[-/TTTGA/TTTGGT]TTTTTGTTTTTGTTT	79589
rs746131523	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106764210	GACCTCGTGATCCAC[C/T]CACCTCAGCCTCCCA	79589
rs746136715	in-del	-/CTT	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106724191	AATTTCTAACTCCTC[-/CTT]CTCTTTCATCCCCCA	79589
rs746146828	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106758313	ATATTCCATGTTCAT[G/T]GATTGGAAGTTTCAA	79589
rs746165661	snp	A/G	2.30859e-05	0.00339741	intron-variant	RNF128	GRCh38.p7	X:106790295	GAGGTAAACATTAAT[A/G]TGTTATTTATATGAA	79589
rs746176476	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106694865	GTGTAAAATGTTATA[A/G]AAATGAGAACTTGAC	79589
rs746185346	in-del	-/AC			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795732	CTGTGTAAATAGAAA[-/AC]TTGAACCATTAGTAA	79589
rs746209301	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106755789	AGGAAAAGAGGAAGT[A/C]AAATTGTCCCTGTTT	79589
rs746215146	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766628	AGCCCTTTGTCAGAT[A/G]GGTAAATTGTAAAAC	79589
rs746218472	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106787459	AAGGTTAACTACAAA[C/G]AGTTTAGAGGAGTTT	79589
rs746255794	snp	C/T	0.245168	0.249953	intron-variant	RNF128	GRCh38.p7	X:106756431	cctcagaaataatgc[C/T]gcatacctacaacta	79589
rs746260044	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106716401	AAACCATAGGGAAAG[A/G]AAACAACTGAGTAGT	79589
rs746263913	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704389	AGTGAGCTGAGATCG[C/T]GCCACGCACTCCAGC	79589
rs746269515	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106697514	CTGAAAATCTACTTC[A/C]CCCACCCTCGTACTG	79589
rs746289176	snp	C/T	4.68329e-05	0.00483883	intron-variant	RNF128	GRCh38.p7	X:106790147	TAGGTAAAGTGTTGC[C/T]ACTTTACAACTGATA	79589
rs746304709	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106743246	TTTTTAAGCAAAAAT[C/G]AGAATTTTGAAAAAC	79589
rs746324597	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106698546	AAACTAACTCAGATA[G/T]GTACATAAAGAAGAG	79589
rs746324606	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770150	CCTTTGTGGGTAACC[C/T]GACCTTTCTCTCTGG	79589
rs746331232	in-del	-/T	2.2805e-05	0.00337668	frameshift-variant	RNF128	GRCh38.p7	X:106773071	TTCGTTTCTGTGTCC[-/T]TTTTTATTATTACGG	79589
rs746425167	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106745309	GGTGATTTGGGTCAC[A/G]TTCCCTGCGATACAC	79589
rs746445611	snp	A/G	4.57854e-05	0.00478442	synonymous-codon	RNF128	GRCh38.p7	X:106694290	GATTGCGCTGATAGA[A/G]AGAGGTAATTGTACA	79589
rs746448404	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758248	GCTCTACAATGAAAA[C/G]TGTAAAACAATGATA	79589
rs746449944	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106792464	CCTCCTGTATTCTTA[A/G]TTTGGATGATAGTAA	79589
rs746450590	snp	A/T	0.0204488	0.0990265	intron-variant	RNF128	GRCh38.p7	X:106704445	TCAGAAAAAAAAAAA[A/T]AAAAAAAAAGAGCTG	79589
rs746494425	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774787	TTTAATGCTTTCAGA[C/T]GAAAATACATTTTTA	79589
rs746501150	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106770075	TTGAATATTGGCCCC[G/T]ACTCTCTTCTGATTT	79589
rs746511881	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716684	TGCCAATCATTTACT[C/T]GCACTTCAAGTGATG	79589
rs746536535	snp	A/C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704232	CGAGGTCAGGAGATC[A/C/G]AAACCATCCTAGCTA	79589
rs746562851	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106718730	TAGCTATAAAATACC[G/T]TATTGTTGAAGGCCT	79589
rs746563264	snp	C/G/T			intron-variant	RNF128	GRCh38.p7	X:106794462	AACCTTTTACAACCA[C/G/T]GATAAGCACTTTTAG	79589
rs746578887	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767235	CTTTAAAGTAGTTTT[G/T]TCCAATTCTATGAAG	79589
rs746598270	snp	C/T	4.56532e-05	0.0047775	missense	RNF128	GRCh38.p7	X:106694139	GCAACTACACTGCAA[C/T]AGAGACATGTGAATG	79589
rs746617808	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106700419	GTTTGCCATTGTATC[C/T]ATTGTACAGAGCATA	79589
rs746655143	snp	A/G	8.46227e-05	0.00650417	intron-variant	RNF128	GRCh38.p7	X:106788029	TCTTCTATATCTTCA[A/G]TAAAATAGCTGACCC	79589
rs746657816	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106718949	AGTCCTGTGCAGCTG[C/T]CACTAATCCTAATGC	79589
rs746669094	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106703039	AATGACATATATTCT[C/T]AGCATGACCTAGCTA	79589
rs746711148	in-del	-/TT	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106730274	CAGTTTATTTCTGTA[-/TT]TTGTTTGCAGAGTAT	79589
rs746719149	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746580	AGTGGATTTCTATAC[A/G]TTGTGAATAATAATT	79589
rs746737339	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766693	GACGGTAGTTTCTTT[C/T]GCTGTGCAGAAGCTC	79589
rs746738429	snp	A/T	2.28206e-05	0.00337784	missense	RNF128	GRCh38.p7	X:106772962	TCTGAAAGGCACAAA[A/T]ATTCTGCAATCTATT	79589
rs746764466	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706878	AGCAAGATGATGCTC[A/G]TGAAGTCATCCTTGT	79589
rs746766251	in-del	-/CCAC	0.0068637	0.0581785	intron-variant	RNF128	GRCh38.p7	X:106699214	GTGGAAAATGTAATT[-/CCAC]CCCAGTTAGAATAAA	79589
rs746779370	snp	C/T	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106762555	TGACCTCAGGTGATC[C/T]GCCCCCCATCGGCCT	79589
rs746796722	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778684	AGTCCCTTCATCTGA[A/G]TCTTGGACCCCAACA	79589
rs746849333	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106755634	TCAATGTCCTACATC[C/T]TATCAACACAATGAA	79589
rs746851799	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106734259	TTTAAATAAAAAATA[C/T]GCTTCACCGAGGTTT	79589
rs746854017	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698153	GTTATTCAAGCAGAA[C/G]ACGCGTAACATGTTA	79589
rs746862616	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106760960	TTTGCATAGCAAAAG[A/T]AACTATCAACAGAGT	79589
rs746863230	snp	A/G	1.6473e-05	0.00286988	intron-variant, missense	RNF128	GRCh38.p7	X:106727371	TCCCCGGGACCCGCA[A/G]TGAGGTCATCCCCAT	79589
rs746865755	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106708143	GATTGGGGTTCCTCG[A/G]CTTGATGACACCATG	79589
rs746872953	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106773822	GGTTGTATGGCATTG[-/T]TCCTGCCACCATTAA	79589
rs746906749	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106734911	TCCTCAGCTACATAC[C/T]GTAGGGAGTTATTAC	79589
rs746907172	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786079	TGACAGGCTGATTCT[A/C]AGCTTAGATGAAAAT	79589
rs746920244	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723713	TGAATGCTAGTTCCC[C/T]GAATGTTCTTTGGAG	79589
rs746953958	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785338	GAACCTGTGCATATT[A/G]CCTTATATGGCAAAA	79589
rs747023043	snp	C/T	2.28251e-05	0.00337817	missense	RNF128	GRCh38.p7	X:106795655	ATGTTGACAACCCAA[C/T]CTTTGAAGAAGACGA	79589
rs747027230	snp	C/G	0.00015178	0.00871015	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106726949	CGGGGTCTCCTGCCG[C/G]GGTGGCTGCGGCTTT	79589
rs747041405	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692592	CCCTCTGCTGAGTGG[C/T]GTGAACTGTTAATTC	79589
rs747058776	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715494	AATGGGGATTTTTTT[A/T]AATTGGCTATCTGCT	79589
rs747082055	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787358	CTCAAAAGCTAGATA[A/G]TGCATGATTCCATTT	79589
rs747082714	in-del	-/AACAAC			intron-variant	RNF128	GRCh38.p7	X:106764677	TCTCAAAAAAAACAA[-/AACAAC]AACAACAACAACAAA	79589
rs747104837	in-del	-/GGAGAGTGA			intron-variant	RNF128	GRCh38.p7	X:106777220	CAGTGTGATACCAAG[-/GGAGAGTGA]CTGGCATGAAGAAGA	79589
rs747106547	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106742788	ACCTCCATGCACTTC[A/G]GGAAACAGAAAGTGC	79589
rs747130799	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106724246	CACCAAAGAACATTC[C/T]CATTCTGCCCACTTC	79589
rs747131877	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106722082	GAGCAAAGGTCCTGG[C/T]GGAGTAGTGATATGG	79589
rs747160559	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106701777	AAACAAGATGAAGTA[C/T]CATGGTGAATAGTAA	79589
rs747178595	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106754410	CAATGTTTTCTTTCT[C/T]TTTTTTTTTTTTTTT	79589
rs747203326	snp	C/T	2.28561e-05	0.00338046	synonymous-codon	RNF128	GRCh38.p7	X:106791134	ATCTAATAGTGCCTC[C/T]TCCCATGAAGAGGAT	79589
rs747246887	snp	A/G	0.00105904	0.0229869	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726830	CCTTCCCCACCTGGC[A/G]CGCACCTGCTCAAGA	79589
rs747265264	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106753258	AGTTTTGAAGACATA[C/G]ACAGTATAATAAGAT	79589
rs747291820	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710383	TCAGAGAACTACAGT[G/T]TATTGAGGATATTGA	79589
rs747300090	snp	C/T	2.50894e-05	0.00354176	intron-variant	RNF128	GRCh38.p7	X:106787871	TGTTCTGTAGTTTAA[C/T]GTATTTTTTCTTATC	79589
rs747303029	in-del	-/C	2.34447e-05	0.00342371	intron-variant, frameshift-variant	RNF128	GRCh38.p7	X:106727266	AAGTCTCTTGGTTGG[-/C]CCTCATCCAACGCGG	79589
rs747331066	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106782719	AACTGTATAACAACT[C/G]TATATTGTAAGGAAA	79589
rs747344514	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106783970	AATACCTCCCACCAC[A/G]CCCCACCTCCAACAT	79589
rs747353462	in-del	-/AG			intron-variant	RNF128	GRCh38.p7	X:106700386	AAGTTCCAGGAAGAC[-/AG]AGACCACGTCTGTCA	79589
rs747366838	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106729555	AGAATCTAACTATGG[A/G]TGTTGTGTTTCAGGA	79589
rs747373769	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106696163	ACACATTGAAAAAGA[C/T]AGCATAATGATCATA	79589
rs747381001	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719604	CACTTCCTTCTACAG[C/T]TCTTCTCTCATTTGT	79589
rs747419654	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106713971	AAGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	79589
rs747425876	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106731942	CATGCCATCAGAACA[C/T]AGCTCTGATCACATA	79589
rs747437382	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106695758	AGGAACCAACTTGCT[A/G]TACATTTAAACTTAG	79589
rs747463519	in-del	-/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106700566	ATTGTATTTTTTAAA[-/G]TTGTTTTTATTTTTA	79589
rs747475495	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771725	GCGATGGCCTGCCCT[G/T]CTCCGTGGGCTGTAC	79589
rs747477494	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764295	ACCTTCATCTGACCA[C/T]AATGGCCCATGTGTT	79589
rs747477802	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106715492	TCAATGGGGATTTTT[C/T]TTAATTGGCTATCTG	79589
rs747505147	in-del	-/TTA	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106737223	GTAGATTTTCTTTTT[-/TTA]TTATTATTATTATTA	79589
rs747523823	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711352	ACCAGACAGTAAGAT[C/G]ATTTTGTTTCATAAA	79589
rs747530518	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771181	TCTGGGAAGTGTCTC[C/T]TAGTTAGGCTACTGA	79589
rs747534982	snp	G/T	3.22794e-05	0.0040173	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727141	CGGCCAGGACTCGCC[G/T]CTGGAGCCTGTGGCT	79589
rs747545487	snp	C/G	2.73654e-05	0.00369891	intron-variant	RNF128	GRCh38.p7	X:106788018	AAGTTTGATTTTCTT[C/G]TATATCTTCAATAAA	79589
rs747560268	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106747593	ATTTGAGTTACTTTG[A/G]CTACATTATACTGTT	79589
rs747566953	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783332	ACAAATATTTGTAGC[A/G]TTTGTAGCAAATATA	79589
rs747574880	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106765166	ACTCAGTAGAGTTTT[A/G]AAAAGGGCTTAACTA	79589
rs747601804	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106787324	CTCAAATGCATTATA[C/G]TAAGTTTAAAAAGCC	79589
rs747627695	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106755354	ACTAATGCCAACCCT[A/G]CTGAAACTATTCTGA	79589
rs747647547	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731547	TTAACCAATGTAAAA[C/T]ACTATTCCCAAAGCC	79589
rs747658563	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106732422	GAAACCTTTGTACTA[C/T]ACATGCTCTAGAAAT	79589
rs747661852	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705411	ACTGGTAGAAACTTA[A/G]TCAAGGCCTTAGGAT	79589
rs747680672	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106734860	CCACAGAAATATTCT[C/G]CTCTTCACTGCACTG	79589
rs747688195	snp	A/C	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106761098	CAACCCCATTAAAAA[A/C]TGGACAAAGAACATG	79589
rs747758027	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106783561	GGGCCTACTTTTTGC[C/T]GAATTTCTAAGTTTG	79589
rs747768876	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106747716	TTTGTTATTTTACAA[A/G]TCATTGGACATTGAA	79589
rs747768915	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106716612	TACCTCAACAAAAAC[C/G]TTAGGAAAAAATCAT	79589
rs747795740	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720824	GATATCATTACCTGT[C/T]GTGAAAATCAAATGA	79589
rs747844912	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106791520	CTTATTAACTAATTA[C/T]AGAGGGTAAGGAGAA	79589
rs747859158	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106767434	AGGTCCTTCACATCC[G/T]TTTTAAGTTAGATTC	79589
rs747927883	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714782	ACCTCAAAAAATGTT[A/G]TATAAATTGAATCTC	79589
rs747932465	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751301	ACAGTGATTGTGGGA[C/G]TTTGCATCAGAACTC	79589
rs747934273	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764168	GACGGGGTTTCACCA[G/T]GTTAGCCAGGATAGT	79589
rs747957566	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786319	AAAGCAATTCAATGA[A/G]GAAAGGATAGCCTTT	79589
rs747980887	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741140	ATATAATTACAGAAT[A/G]CCCTATTTATCAATA	79589
rs747984682	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106705611	ATAGGATGTTTGATA[C/T]TGTTTTAGCTCTAAA	79589
rs748010503	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106776807	CTAGTAGGAATAGAA[C/T]TAATACTGAATGATA	79589
rs748023021	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106723632	GTTCTGGCACAAGTT[A/G]TTTGACTAGCTTCAC	79589
rs748052639	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787017	GAGAATGCAAAATGT[-/A]TAGCCAATTTGAAAA	79589
rs748089358	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106778629	GGGTCCTCAGTTTCC[G/T]GCAACATGGCCAGTT	79589
rs748101006	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106774852	TTCTGGTCACTTCAT[A/G]TACTCTTCCTCCAAT	79589
rs748109366	snp	G/T	2.35646e-05	0.00343246	missense	RNF128	GRCh38.p7	X:106694054	CTTGTAATTTTTACC[G/T]TTTTACTTAAAATTA	79589
rs748160862	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789919	TGAACAAAGTCTTAG[G/T]TCAGGTAGTGTCCTA	79589
rs748161424	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752238	CATAAGCCTTGGGCA[A/C]AACCCAGAACTATGC	79589
rs748194045	in-del	-/AA	7.70456e-05	0.00620619	intron-variant	RNF128	GRCh38.p7	X:106694429	TAATAATTGATTCAC[-/AA]AGAGAGTTAATGTCC	79589
rs748203258	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754562	AGCATGCCCAGCCAA[A/C]ATTTTTTTTAAATTG	79589
rs748212761	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706804	AATTACATAATGCAT[A/G]TAAAGAAGGCACTTT	79589
rs748258674	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106741422	TGAAACTGAGGTATA[C/T]CAAAGCCCCATGTTG	79589
rs748261163	in-del	-/ACAAAA	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106733575	CATAGGCATAACTTT[-/ACAAAA]GTATTCTACTTTTGT	79589
rs748268094	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106716451	GAAGGGGTTTTGACT[A/G]TAAAGGCATAGCATG	79589
rs748273121	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106696996	CTAGTTTGCTTGAGA[C/T]TGAAGGTTTCTTGGG	79589
rs748288456	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106739267	CGGGTTCAAGCGATT[A/C]TCCTGCCTCAGCCTC	79589
rs748296944	snp	A/T	0.0495675	0.149422	intron-variant	RNF128	GRCh38.p7	X:106788381	ATATATATTATATAT[A/T]ATATATAATATATAT	79589
rs748300945	snp	C/G	0.283335	0.247768	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693397	ACACACACACACACA[C/G]ACAGAGAGAGAGAGA	79589
rs748302662	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106695684	ACGAGTGACTTTCAT[C/T]TTTGTAGAAAGAAAC	79589
rs748313304	in-del	-/AATA	0.000530926	0.0162844	intron-variant	RNF128	GRCh38.p7	X:106744760	CACCAAGCCCAGCCG[-/AATA]AATAAATAAATATTT	79589
rs748476987	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106748384	GCAACATAAACAACA[C/T]AGATTCAGTGATATG	79589
rs748481855	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106749016	AACTATGATACATCA[A/G]TTTTTAAAAAAGGAA	79589
rs748526213	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711840	CAATTATGAGAACAC[C/G]AAGACACTCAGCCAA	79589
rs748528622	snp	A/G	0.00018558	0.00963098	intron-variant, missense	RNF128	GRCh38.p7	X:106726938	CCGCCTGGGGCCGGG[A/G]TCTCCTGCCGCGGTG	79589
rs748534186	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106728025	GAGTTGCAAAACAGG[A/T]GACTAACGTTCTTGA	79589
rs748534247	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106750327	AACAGCTTTAGGTTT[A/C]ATTGAAGATAACTAG	79589
rs748534806	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106712069	CCTGCATGTGGCTAG[C/T]CCACCGGTGGTGGTT	79589
rs748535226	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106736329	CAAGAAACTGTCAAG[-/T]TCCAAGGTTGCTTTG	79589
rs748572168	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106749905	GCGAGACCTTGTTTC[-/A]AAAAAAAAAAAAAGG	79589
rs748583455	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106729330	TGTGTCCTTGGTAGG[A/T]TTATTTAACTTTACT	79589
rs748646337	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765846	ATTTATATTAGGTTT[A/T]TCTCCTAATGCTATC	79589
rs748652053	in-del	-/GC	0.000428816	0.0146364	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726902	CTAGGGAACTGCGGA[-/GC]GCGCGCGCGCCATGG	79589
rs748670788	snp	A/G	2.61736e-05	0.00361747	intron-variant	RNF128	GRCh38.p7	X:106694446	AGAGAGTTAATGTCC[A/G]TTTATCTTAGAATGG	79589
rs748674931	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702902	CTCAGGACATGCTTT[A/G]AGCACACAAATATTC	79589
rs748706946	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106738397	TCTCCATTGGTTATT[A/G]TAGATATTTACTACC	79589
rs748728638	snp	C/T	2.35178e-05	0.00342904	intron-variant	RNF128	GRCh38.p7	X:106773175	GGTTTGTAATGGTCC[C/T]TTCTTCCACTATTAA	79589
rs748750556	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772478	TAGTAGTGAGCTCTT[G/T]AGATAATTTATCATC	79589
rs748751415	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720940	AGTTTTAGATACAGC[A/G]TATCTACTGTTTGTA	79589
rs748774073	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106729981	TTGCTGTGAATTACG[A/C]AGGGGCCACCAAATG	79589
rs748776501	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751087	CAAATTGAACAACTC[C/T]CCACACAAGAAAGCA	79589
rs748778487	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106776289	AATAGCCACAATGCA[C/T]GTGTTGGATTAAACA	79589
rs748781359	snp	C/T	0.0152462	0.0859689	intron-variant	RNF128	GRCh38.p7	X:106721751	TCTCCAGAGGGAAAA[C/T]AGTTAAGTCATTATC	79589
rs748792220	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696930	CAGGATTTGGGCTTG[C/T]TTATGTGTTTTGGGG	79589
rs748802554	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106793903	GTCTGCCAGGTTTCT[C/T]CCTTTAAAGTTACTA	79589
rs748807369	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733461	TAAAATTAACTGTTA[C/T]AGAAAACTTGAAAAA	79589
rs748829895	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106752481	TGCAAGAGCCACAGC[A/G]TTACTGGGCTTGGGG	79589
rs748877779	snp	A/G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750084	CTGAGTGAATAATCA[A/G/T]TTGTACTTAAGTTTT	79589
rs748978170	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106795306	GGAAGAAGTAGAAGA[C/T]ATAATTTTTGCTCTT	79589
rs749004317	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762350	GATGGAGTTTTGCTC[C/T]TGTTGCCCAGGCTGG	79589
rs749026234	in-del	-/G	0.00896606	0.0663524	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726751	CATCTGCGGCAACCT[-/G]TGTGCTGACGCTACG	79589
rs749067247	snp	C/G	2.37113e-05	0.00344312	intron-variant	RNF128	GRCh38.p7	X:106791247	CAAGTAAGCATCATA[C/G]TAAAGGTTAACGAGT	79589
rs749081209	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106739097	CTTAACAATTTCTCT[C/G]TTCTATTCTCTTCTC	79589
rs749130379	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106720494	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	79589
rs749134039	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106740659	ACTGCAGCCTTGAAC[C/T]CCTGGGCTCAAGCAT	79589
rs749138937	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768529	TAGTATTCTCTGATG[A/G]TAGTTTGTATTTCTG	79589
rs749139694	snp	C/T			downstream-variant-500B	RNF128	GRCh38.p7	X:106797376	CCCCACCAGGCCTCA[C/T]CCCCGACATTGAGAA	79589
rs749155323	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706396	TATGTGAAAAAAAAA[A/C]AAAAAAAAACAAGGG	79589
rs749181064	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760368	CATACAAATAGCCAA[A/C]AGTTACATGAAAAAA	79589
rs749194806	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777278	TTACTATATTAAATT[A/G]CTCTGTGCAAGTCTA	79589
rs749197154	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106705362	CTAATGCTAATTACC[C/T]ATCTGCATTGAGGAG	79589
rs749210957	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106703859	TTTTGGAGGTTTAGC[A/G]GATTAGGATGCTGAT	79589
rs749220813	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732766	GGTAACAAGAAAATA[A/C]TGACAAATGACTTTT	79589
rs749221818	in-del	-/TGT			intron-variant	RNF128	GRCh38.p7	X:106778207	TGCCTATAACTGCCA[-/TGT]TGTTCAAGGGTCAAC	79589
rs749239363	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696344	AATAGTGTGCCATTG[A/G]ATTTTTTCCTTCCTA	79589
rs749261938	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767689	ACTTCCTCTTTTCCT[A/G]ATTGAATACTCTTTA	79589
rs749298086	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106774254	AAATTGAAGCAATCA[A/G]TAATACTTCCACATC	79589
rs749319766	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106781134	TCTAGCCACTGGGGA[A/T]TTTTTTTCTAAGTGA	79589
rs749366217	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106709172	AATAATTTCATAATG[A/C]AAGTAGGCTTCTATT	79589
rs749373168	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106781930	CTGTTCTCCTGGGCA[G/T]AGACTCAGACATTAC	79589
rs749375544	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106727538	ACGGAGTGGGGCAGG[A/G]TCCTCCCCGAGATTC	79589
rs749390711	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106718578	AGATGTGATTTTATA[G/T]ATGCCAGGGTGTGCT	79589
rs749392654	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106707731	AAAATTTCATCCTTC[A/T]TTAAAACAGCATTCT	79589
rs749413876	snp	G/T	2.41453e-05	0.00347448	intron-variant	RNF128	GRCh38.p7	X:106791023	ATGTCGAGGAAAAGC[G/T]TGTACACTGAGAGGC	79589
rs749418395	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106761433	CCATTATTGGGTATA[C/T]ACCCAAAGGAATATA	79589
rs749419584	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711589	CATTTTTTTGTTCCA[A/G]CCTTATAAAAGAAAG	79589
rs749451330	snp	A/G	2.30203e-05	0.00339258	intron-variant, missense	RNF128	GRCh38.p7	X:106727361	ATCTTTAACTTCCCC[A/G]GGACCCGCAATGAGG	79589
rs749457865	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106699248	ATCCAGGCCTTGAGC[C/T]TAGGCCTACAAGGTT	79589
rs749459493	in-del	-/TTTGCCATA	0.0126344	0.0784702	intron-variant	RNF128	GRCh38.p7	X:106723210	ATCACTTGTTGTCAT[-/TTTGCCATA]TTTGCCATATTTGCT	79589
rs749472463	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693482	GCCATAGCAATTAAA[C/T]TCATGGATCTTAACT	79589
rs749482330	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770113	TTCTGCCGAGAGATC[C/T]GCTGTTAGTCTGATG	79589
rs749483591	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770684	TTACTTCTTTGCGAT[A/G]GGTTCGAACATCCTC	79589
rs749572717	in-del	-/TTAG			intron-variant	RNF128	GRCh38.p7	X:106737195	AACTTGATTTGTGGC[-/TTAG]TTAGTCATCAGTAGA	79589
rs749612435	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106745690	TGATAGTAAATACAT[-/A]TATATATTGCAAGAA	79589
rs749614382	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693450	GAGAAAAAAGCAATA[A/C]AATTCATTCTACTAA	79589
rs749624331	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106769429	TATATTTAGGATAGT[C/T]AGCTCTTCTTGTTGA	79589
rs749638937	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106773446	TCTTTTAAATAAACA[-/T]TTTTTTTCTAAATTA	79589
rs749641912	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746098	TTCTGGATATCAGCA[A/G]ATTCAGAAGTGCTGA	79589
rs749657356	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106718478	ATATTTTGATGTTAA[C/T]TGCACCCAAAGCTAC	79589
rs749680552	snp	C/T	2.29798e-05	0.0033896	missense	RNF128	GRCh38.p7	X:106791103	TGTCTTTACAAGTCC[C/T]TGTATCCAATGAAAT	79589
rs749692774	snp	C/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726185	ATACACATGTATGAG[C/G]CTTCTTAGGAGCAGG	79589
rs749734139	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106755759	GCAGGAGAAGGAAAT[A/G]AAGGGTATTCAATTA	79589
rs749734953	snp	C/T	0.000140415	0.00837781	missense	RNF128	GRCh38.p7	X:106694328	AAAAAATTCAAACAG[C/T]GGGCAGAAGAAATGC	79589
rs749779005	snp	C/T	2.32358e-05	0.00340843	intron-variant	RNF128	GRCh38.p7	X:106790318	TATATGAAGAATATA[C/T]GCCTGGGCTTTGGAG	79589
rs749795237	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106729681	AAGGCTATACCAAAG[C/T]TTGCCATCAAGCTAA	79589
rs749806791	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717652	TTATTTTAAATCACT[A/G]AAACTCCAAAATAGA	79589
rs749864044	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766160	ATGCTATTGTGAATA[A/G]TGCCGAAATAAACAT	79589
rs749924401	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106765818	GTGTGCTGCACCCAT[G/T]AACTAACTCGTCATT	79589
rs749937431	snp	A/C	3.72356e-05	0.00431468	intron-variant, missense	RNF128	GRCh38.p7	X:106726921	CGCGCGCCATGGGGC[A/C]GCCGCCTGGGGCCGG	79589
rs749954563	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735850	ACTTTTCCTATTTTA[A/T]TATGGAATCTTTCTC	79589
rs749980305	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770507	TTCATTTGATCTTCA[A/G]TCACTGATACCCTTT	79589
rs749984429	in-del	-/TTTGG/TTTGGTTTGG	0.363972	0.222509	intron-variant	RNF128	GRCh38.p7	X:106763927	TGCCTATCCTTGTTT[-/TTTGG/TTTGGTTTGG]TTTGGTTTGGTTTGG	79589
rs749990844	snp	A/C/G/T	9.21089e-05	0.00678586	missense	RNF128	GRCh38.p7	X:106791193	ATGCTTCAGTACAGG[A/C/G/T]AACAGATGAACCGCC	79589
rs749993356	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106721423	CATCTCTATAGAGTC[A/G]GTGTGATGGGAAACT	79589
rs749994431	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106722857	AAGTAGGGTTGCTCG[A/G]TGAGGATGAACTCAG	79589
rs750003819	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709629	TGGGCTCACCGCAAC[C/T]TCTGCCTCCCGGGTT	79589
rs750004331	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774621	TATTATTTCTACCTT[A/C]ATTATATATCCAGAA	79589
rs750034610	in-del	-/CA			intron-variant	RNF128	GRCh38.p7	X:106730530	AAAATGTAAGATTGT[-/CA]CGAGACACGTTAAGC	79589
rs750049490	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106706270	GATTTTCCAAATTGG[C/G]AATAAAAGAAGGCAA	79589
rs750065527	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751931	GACCCAGCACATTCC[A/C]AGCTGTAGTGGCCAA	79589
rs750121546	snp	G/T	2.36055e-05	0.00343543	missense	RNF128	GRCh38.p7	X:106791067	CATGTTCTTTAAAGG[G/T]GGATGTTGAAGATGG	79589
rs750124343	snp	C/T	4.63575e-05	0.00481421	missense	RNF128	GRCh38.p7	X:106785113	GGAAGGCTTCAACTA[C/T]GCACACTGAAACAAG	79589
rs750148941	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717929	AACTGGACAATAGCA[A/G]GCAGTATAAATCTAC	79589
rs750199924	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106729350	TTAACTTTACTGAGC[C/T]TTGGATACCCCATCT	79589
rs750248715	snp	A/G	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106717362	AAGGCTATTTACAAT[A/G]ATCTAAAAAAAATTA	79589
rs750251807	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766350	GTTAAAGGAGTTCCT[A/G]TTTCTCCACATCCTC	79589
rs750302145	in-del	-/GACCACAACACTGAGTTTAGTAATACTAA	2.28363e-05	0.003379	frameshift-variant	RNF128	GRCh38.p7	X:106694237	AACTACCAAGCTTGT[lengthTooLong]GAAGCCCTGGATTGC	79589
rs750304585	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106694908	TTGTAAGATTTGAAT[C/G]TTTTTGCGGGACTGA	79589
rs750308193	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106770050	GTGGGTTGAAAATTC[C/T]TTAAGAATGTTGAAT	79589
rs750322564	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106734099	CTATTGTAAGAATTT[A/C]TCCATGTATCTAGAA	79589
rs750341566	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708556	AAATGTGGGGTTAGC[A/C]CTTAGAGGAGTGAGG	79589
rs750361218	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106745810	ACTTTGAAGAAAGAG[A/T]GGCTAGTTTGGCTTA	79589
rs750364745	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106714706	AGCCAAAAGGACCTC[C/T]GCCCCGTAACCCCTT	79589
rs750387439	snp	A/G	7.4898e-05	0.0061191	intron-variant, missense	RNF128	GRCh38.p7	X:106727058	ACCGCGTACCTCAAC[A/G]TGTCCTGGCGGGTTC	79589
rs750399082	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106757643	AATGCTAGATGACGA[G/T]TTAGTGGGTGCAGCG	79589
rs750406005	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106696660	CCTCAGGCCCTTGTA[C/T]TCTTCTACTCTTCTC	79589
rs750467415	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106771232	GGAGGCAGTCTGTCC[A/G]TTCTCAGATCTCAAA	79589
rs750470189	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106783259	ACAGGTTTGGGCATC[A/G]ATGAGATTCCTCACC	79589
rs750493151	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106794244	CCTTGCTCATATCAT[C/T]CTAGATTTGGTCATT	79589
rs750522360	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106747833	TAGATATATACAATT[A/C]ATTTCACTGGCTTGG	79589
rs750534701	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696572	TACAATAAAGCTCAC[A/G]ATTTCACCTTCTGTC	79589
rs750562960	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760814	ACTATTCAGCATTTA[A/G]AAAGCAGCAAATCGT	79589
rs750627275	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106734706	TGTGTGACCAGCGCC[A/C]TGCTCAAGGAATAAA	79589
rs750634375	snp	C/T			intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727342	AGGGGCGTCTGGAGC[C/T]GTCATCTTTAACTTC	79589
rs750640268	snp	C/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106712216	AAAGCCAACTTCGAG[C/T]GTCTTTTTATTATCT	79589
rs750689534	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106728625	TTATGACTGAACCTG[C/T]CTAGAGAGCACTTGT	79589
rs750692897	snp	A/G	2.2837e-05	0.00337905	missense	RNF128	GRCh38.p7	X:106694246	GCTTGTGACCACAAC[A/G]CTGAGTTTAGTAATA	79589
rs750702545	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784114	CTACTTCAATTCATA[C/T]GTATATTATATTCAC	79589
rs750737241	in-del	-/AC	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106741806	CTAGTTGCTATAGAT[-/AC]AGTGATGAAAGACCT	79589
rs750740477	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106734641	ATACATCCCAAAAAG[A/G]TACATAAATCATTGA	79589
rs750749827	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731088	ATAATGCAGATAAAG[C/T]GTTTAGCACAGTGTC	79589
rs750756385	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106705108	AGGGAGGTAGGGTAC[A/G]GTGGAGGGTAACAAG	79589
rs750780462	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775861	TTCAAGAATTTCTTC[C/T]TTCTGAAGGTTATGA	79589
rs750805340	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752659	CAAGCACCAAGAAAT[A/G]TCCACAAGCATCCAG	79589
rs750808283	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106759341	TGTTGGTTGGAATGT[A/G]AATTACTACAGCCAC	79589
rs750852715	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106737949	TTTTGCTGCTCCTCT[A/G]TGGCTGATGCTTTTT	79589
rs750856615	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106793292	TGGAGAGATTTTAAA[C/T]TTTGCTGATGTTTGG	79589
rs750860158	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692370	AAATTGACCATAAGC[C/T]AATACACAAGACCTT	79589
rs750877894	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106715120	GAAACTGCCAGACTG[C/T]TTTCCAGATTGGCTG	79589
rs750880106	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106793796	GAAGTGATGTTGTGC[C/T]CCTTTCAGTGCCCCC	79589
rs750895153	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106717897	GCAATGAGTGACAAG[A/G]GTAAGATTCTGTTGC	79589
rs750906473	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106768144	GAGGATTTTTGCATC[A/G]TTGTTCATCAGGGAT	79589
rs750918154	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706111	CACGACATGGGAGAC[A/C]AAGGGATGAAGAGAA	79589
rs750922463	snp	A/G	2.29801e-05	0.00338962	missense	RNF128	GRCh38.p7	X:106772933	GTAGACATTGTTGCA[A/G]TCATGATCGGCAATC	79589
rs750934789	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106699609	CAAAACATATAGGTC[A/G]ATCACATCACTCCTC	79589
rs750950110	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106695876	ACTAAATAGTAGTCC[A/T]GTTTTCAAAACTTTC	79589
rs750961717	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106776774	CTGATCTGGACCAAA[A/G]GATGGGCCAAAATAA	79589
rs750996000	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725947	AGTGAATCGCCTAGG[C/T]GAGTCAGGCTCCTTT	79589
rs751021304	snp	A/T	7.16692e-05	0.00598577	intron-variant	RNF128	GRCh38.p7	X:106791051	GGCTTTTAATTTGTT[A/T]CATGTTCTTTAAAGG	79589
rs751037901	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106767192	TAGGATTGTCTTGGC[A/G]ATGCGGGCTCTTTGG	79589
rs751044216	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786908	CAATGAAATACAACT[A/G]CGCATTCATTAGAAT	79589
rs751048257	in-del	-/AGG	0.00581083	0.0535878	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692081	TGAGAAGATTTTTTA[-/AGG]AGTAATTTAATTGGC	79589
rs751075604	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106762473	CATGCACTGCCACGC[C/G]TGGCTAATTTTGTAC	79589
rs751085545	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106741873	AATAAACCAGATAAC[-/T]TTTAAGGGAAGTCTG	79589
rs751094465	snp	C/T	2.28841e-05	0.00338253	synonymous-codon	RNF128	GRCh38.p7	X:106790249	GACTTGCCCCATGTG[C/T]AAATGTGACATACTC	79589
rs751102026	snp	C/G	0.00949095	0.0682305	intron-variant	RNF128	GRCh38.p7	X:106752082	TTCCTGACTCCAGAC[C/G]CTACCTCCCAGACAG	79589
rs751128549	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106738535	ATCAAGAAACTGAAA[C/T]GACTATATTATCTTC	79589
rs751148814	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777056	TTTCTGTGACATTTC[C/T]GGATTTTTTTTGTAA	79589
rs751159853	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741919	AAGCAGGACATCTAA[C/T]GCAGTCAGGTCAGAA	79589
rs751213689	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106719978	TCCCCAAATAGTTGT[A/T]TTTCTTTCTTTAATA	79589
rs751223071	snp	A/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796927	CTGATTTGAAATGCT[A/G]TAAATATGTCCCAAT	79589
rs751245709	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709773	CTGATCTCGAACTCT[C/T]GACCTCAGGTGATCC	79589
rs751272994	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106721294	CATCACTTAGATGCC[A/T]GGATACCGTTTGTCC	79589
rs751273232	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106775960	AGCCCCCAGACAGAA[A/T]AGCCTCATATGTTGT	79589
rs751278131	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106782272	GACATCATCAACTAC[A/G]TTACATTTTTTCCCC	79589
rs751360133	snp	C/T	1.91075e-05	0.00309085	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726908	GAACTGCGGAGCGCG[C/T]GCGCCATGGGGCCGC	79589
rs751361392	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106781189	CAAGAGAGAAAGGCA[C/T]ATTAATAATACAATT	79589
rs751383527	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759157	TCAAAAGAAGACATA[C/T]AAAAGGCAAACAGGT	79589
rs751389606	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106746032	GTTCCAGATTTTATA[A/G]TGGAGGAAATGTTTG	79589
rs751429346	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708613	AAACTCTTTTAAGTA[C/G]TATATAGAAGCAACT	79589
rs751450955	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106783091	TTTAGGGTCTAGGCC[C/T]TCCTATTCACTGTTT	79589
rs751473097	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771560	CTCTGAGCCAGGCGC[A/G]GGTTATAATCTCCTG	79589
rs751473247	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764123	GCCCGCCACCACGCC[C/T]GACTAATTTTTTTTT	79589
rs751497480	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106728290	TAGCAGTGTATCATA[A/G]TTTTTAAGAGCTGGG	79589
rs751501240	snp	A/C	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106735910	TTTTACCCTCCCCCC[A/C]ACACACACACACATA	79589
rs751512996	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106736693	TGATAAATTTGATGT[A/G]CCTTTGTTTTACTTT	79589
rs751544934	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747165	CTACAAATCAGATAG[A/G]CATTTAACAAATAAA	79589
rs751545562	snp	A/G	2.46783e-05	0.00351262	missense	RNF128	GRCh38.p7	X:106694390	ACTGGCAATCAGACG[A/G]TACAGATGGCAAATT	79589
rs751552070	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702725	GGGGGAAAGATTTAC[G/T]TGTTGCACCTAGAAA	79589
rs751587609	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106790987	TCCAATGAGTCACCT[A/G]TAAAGAAACTTTGAA	79589
rs751640141	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784798	CCATTAGGGGTGGGG[A/G]AAATGTATTTTTACC	79589
rs751649027	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106712258	TCATCTGCATCACTG[A/C]TTCCCATCTACTGGT	79589
rs751718996	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749809	ACTCAGGAAGCTGAG[A/G]TGGGAGTATCACTTG	79589
rs751754851	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106749447	CAGAAACACACAACA[C/G]CACACAAAAAAGCAC	79589
rs751763770	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106745673	TCTTTGATGAGGTAC[A/G]CTGATAGTAAATACA	79589
rs751790578	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789581	ATAATATGTAGTATA[G/T]ATAGTTACACATGTA	79589
rs751803593	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728050	TCTTGAAAAAGAAGA[C/G]GTTTCTGCATGAGGA	79589
rs751808979	in-del	-/CAGT	2.33984e-05	0.00342033	frameshift-variant	RNF128	GRCh38.p7	X:106791225	CTGGAGGAACACGTG[-/CAGT]CAACAAGTAAGCATC	79589
rs751838290	snp	A/C	2.40422e-05	0.00346706	missense	RNF128	GRCh38.p7	X:106787970	TTGAATTGTATAAAC[A/C]AAATGATTTGGTACG	79589
rs751843573	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693274	CACTATACTTGAAAG[A/G]AAAGGAATTCTAGCT	79589
rs751867916	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106752367	AGATTCCTTTTGTTT[A/G]AGAGAAAGTAAGGGA	79589
rs751877459	snp	A/G	0.000206119	0.0101497	missense	RNF128	GRCh38.p7	X:106773132	CTGCTCGAAGGCTAC[A/G]GAATGCAAGAGCTCA	79589
rs751879833	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739047	CAAATACTTAACATC[C/T]GAAATACGATTTGGG	79589
rs751907525	snp	A/G	2.50269e-05	0.00353735	intron-variant	RNF128	GRCh38.p7	X:106772879	TACTAAGAATGTTTC[A/G]CCAAACTAAAACTGA	79589
rs751925917	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732515	GAAAAGTATCTAGTG[G/T]ATCGGAATTCAATTC	79589
rs751939017	in-del	-/TT			intron-variant	RNF128	GRCh38.p7	X:106767202	TGGCGATGCGGGCTC[-/TT]TTTGGGTTCCATATG	79589
rs751951683	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106761954	TGTCTTTTTTTTTTT[A/T]AAGACCCTTAATTTA	79589
rs751960500	snp	G/T	2.3161e-05	0.00340294	intron-variant, missense	RNF128	GRCh38.p7	X:106727295	GGCGGGGGCTGCACC[G/T]TCGCAGACAAGATCC	79589
rs751969638	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106777921	GTTGCAGTGAGCCGA[A/G]ATCATGCCACTGCTC	79589
rs751974108	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784213	TTCAAATTGACAAAT[A/T]TCTTAACAAATATCA	79589
rs751979338	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768285	GAATAGTTTCAGAAG[C/G]AATGGTACCAGCTTC	79589
rs752013671	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106697382	CATAGTCACAGATTG[A/G]CCTTCTCTAATGTTG	79589
rs752019942	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707507	TGTTAGAATTTCAAT[A/G]TTTTTACCACTAAAA	79589
rs752021246	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106735767	TCCATATGATAGTTG[A/G]TGTTACCTTTTATTG	79589
rs752025412	snp	A/T	2.41651e-05	0.00347591	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795763	ATAACAGAACTGCCA[A/T]TCAGGGCCTAGTTTC	79589
rs752069027	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106734067	ATACTATATATACTA[A/G]TTTTGTATACTGCTT	79589
rs752077431	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106716281	CACTCTTTTGTTTAA[A/G]TACCACACCAACGCA	79589
rs752080641	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717130	ATGGCGTGGACCCGG[A/G]AGGCGGAGCTCGCAG	79589
rs752112993	in-del	-/TCTGTAAG	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794351	GATTAGCCAACTTTT[-/TCTGTAAG]GGGCCACATAGTAAA	79589
rs752129514	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789234	TAAATTCCAACTAAG[C/G]AGTGAACACTTCCAA	79589
rs752148767	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106761032	ATGCATCCAACAAAG[G/T]TCTGATATCCGAAAT	79589
rs752169556	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777185	AAATATATTTGAGAC[A/G]TTGAACTAAAAACTC	79589
rs752221749	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106762231	CCTAACTGTAAGTTT[A/G]TACACATTGGCCAAC	79589
rs752250891	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106780526	AATATTCTTAGACCA[C/G]GTATCTCTTAGGATT	79589
rs752269360	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106760865	TGAACCTGGAGGAAA[G/T]TAAGTGCCAAAAGCA	79589
rs752279870	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769244	TCTGCTTGGTGCAGC[A/G]CTAAGTTCAGTTCCT	79589
rs752291117	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733327	AATAACTTTTCCCCC[A/C]TCAGTCCCTGGAAGA	79589
rs752327200	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692740	TTTCGGTTGTCCTGT[C/T]CCCTTGACTCTAGTA	79589
rs752354004	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106794599	TTACTGGAGAATAGT[A/G]TTTCAAAACCAGGAT	79589
rs752402392	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106777774	CAGGAGTTCCAGACC[A/G]ACCTGTGCAACATGG	79589
rs752411932	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106771645	CGATTTTCCAGGTAC[A/G]GTCTGTCACGGCTTC	79589
rs752413321	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696826	TGTAGTTTAAAAAGG[G/T]AGATTTATTACTTGT	79589
rs752477232	snp	A/G	2.41351e-05	0.00347375	intron-variant	RNF128	GRCh38.p7	X:106791025	GTCGAGGAAAAGCGT[A/G]TACACTGAGAGGCTT	79589
rs752477999	snp	A/C	2.45438e-05	0.00350304	missense	RNF128	GRCh38.p7	X:106694387	GAGACTGGCAATCAG[A/C]CGATACAGATGGCAA	79589
rs752483433	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106745090	GTGTCATTTCTAATT[C/T]CCTAATGTCTTTAAT	79589
rs752489321	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106699371	ACAAAGAGAAATAAG[C/T]GCAAGCTTTTGTACT	79589
rs752490402	in-del	-/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106736927	TTTTAAAACATAACC[-/T]TACTAGTGTTTCTAT	79589
rs752528648	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106742545	CGTTTGAGGATCATC[A/G]ATCCAGCACAATGGT	79589
rs752529435	snp	C/T	2.28412e-05	0.00337936	synonymous-codon	RNF128	GRCh38.p7	X:106694260	CACTGAGTTTAGTAA[C/T]ACTAAGAAGCCCTGG	79589
rs752534202	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725482	AAATTTAACAAATGT[C/T]GAGCTGCATAAAGTA	79589
rs752618888	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765760	CTAGGCTACATGTGC[A/T]CAACATGCAGGTTTG	79589
rs752621755	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752973	CAAGCAGAAGAAAAA[A/G]GTATTGAGCTTGAAG	79589
rs752640592	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764890	TGGCTCTTAGAGAAA[A/G]GACAAATAATGTCTG	79589
rs752641926	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106708013	TGATGAATGAATAAA[G/T]GAGTGTATGAAAATG	79589
rs752643017	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106707079	TTTTGCCTTTTTGCC[-/T]ATTTTTATGTATTCT	79589
rs752643261	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787763	ACTTTTAAATCACCT[C/T]TGGGAACTTTACAGT	79589
rs752675066	snp	A/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795943	CCTCTCAGTAGTGAT[A/G]ACAACATTTTTAGAC	79589
rs752688195	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702464	AATACACACAGAACA[A/G]TGCCTGAGCCTATAT	79589
rs752695942	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106766113	CTTAATCCAGTCTAT[C/T]ATTGAAGGACATTTG	79589
rs752745403	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106772171	CAAAACTTATATAAT[C/T]GGTGGTAGAGAGGTA	79589
rs752796382	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774291	TCTATCTTCATCTGC[A/G]TCTATCCTATTCCCC	79589
rs752815451	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704025	AATGATAATGTCTTC[A/G]ATAAATGTGTGAAAA	79589
rs752819161	in-del	-/TT			intron-variant	RNF128	GRCh38.p7	X:106795034	AGAGTCAAAATACTG[-/TT]TTCCAAAGTTATTTA	79589
rs752832234	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106786941	CTAAAATGCATACAA[C/T]TGAAAATACCAAGAG	79589
rs752832507	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739827	TAGATTTTTTGGTAC[C/T]TATATGATACCAAAA	79589
rs752839851	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106714276	TGATTTTTTTTTATG[C/T]TTTAAGAAAATATGC	79589
rs752862792	snp	A/G	4.62829e-05	0.00481033	missense	RNF128	GRCh38.p7	X:106785092	GCAGATGCTAAAAAA[A/G]CTATTGGAAGGCTTC	79589
rs752900867	in-del	-/T/TT/TTTT	0.49161	0.0642225	intron-variant	RNF128	GRCh38.p7	X:106769546	GCTACACCTGCTTTG[-/T/TT/TTTT]TTTTTTTTTTTTTTT	79589
rs752920220	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106789946	CCTAGCCATTTTCAA[A/G]TGAGTACTGAAAATA	79589
rs752929172	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106780803	AGATAGAACCTGGGC[G/T]TGAATTGAATCACAG	79589
rs752938738	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730923	ATTGTTGAAAGATAG[C/T]GGAACAGATTAGTTA	79589
rs752964327	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790856	ATGAGAGTGCACTCC[A/G]CCTATAGCATCTTTC	79589
rs752968456	in-del	-/TTA	0.0105399	0.0718252	intron-variant	RNF128	GRCh38.p7	X:106694553	CAACTTGTAATTACT[-/TTA]TTATTATTATTTAAT	79589
rs752972418	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106698083	CTTTTCCGAGCACTG[A/C]AGACATGGCCTTTCA	79589
rs753005437	snp	A/G	2.37169e-05	0.00344353	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795741	TAGAAAACTTGAACC[A/G]TTAGTAATAACAGAA	79589
rs753018876	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106721650	ATATCTCCCTCAATG[A/G]TCACAGTGCCTGAAA	79589
rs753064286	in-del	-/CC	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106722554	AAAACCAGTGGGTTA[-/CC]CAGGCAAGTCTCCAT	79589
rs753102174	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796179	CAATGCAAACTTAGG[C/T]GAGTACTTCTTGAAA	79589
rs753102578	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106773271	AATGATCTCCCCATA[C/T]GTTTTACAAAATCTG	79589
rs753115544	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733985	GAATTACAGGCGTGA[G/T]CCACAGTGCCCAGCT	79589
rs753123809	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762285	GTACCCTCCCCAGCC[C/T]CTGGTAATCACTATT	79589
rs753129012	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750562	AGAAATCCAGTGCAT[A/C]GCCAGGATTCAGGAA	79589
rs753132059	snp	A/C	2.28264e-05	0.00337826	missense	RNF128	GRCh38.p7	X:106795636	GCAGTGGATGTTATT[A/C]CTCATGTTGACAACC	79589
rs753179493	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106713347	AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA	79589
rs753183809	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106704810	AGCTAAGGATGGAAT[C/G]AATGTGATACCAGGT	79589
rs753225208	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708272	TAGGCTGTTTCTATA[C/T]AAAGCTCTGGCAGTA	79589
rs753236963	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706141	AACCCTAGGGTATGA[A/G]CCCCTGGGTTGCTAT	79589
rs753238726	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763022	TGAGATCAGATCATA[G/T]ATGGCTTTACATGTT	79589
rs753245428	in-del	-/TTCC	0.080205	0.183493	intron-variant	RNF128	GRCh38.p7	X:106739133	TCCTTCCTTCCTTTT[-/TTCC]TTCCTTCCTTCCTTC	79589
rs753261320	snp	C/T	2.5344e-05	0.00355969	synonymous-codon	RNF128	GRCh38.p7	X:106694008	TGAATGAGCAATGAA[C/T]CAGGAGAATAGGTCC	79589
rs753265795	in-del	-/TCTA	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784997	TATTTATTGATCCTC[-/TCTA]TCTTTTTCATCATAC	79589
rs753298412	in-del	-/G			intron-variant	RNF128	GRCh38.p7	X:106744893	AAGGGGTCCTGAGAC[-/G]CAAAAAATTGGAGAA	79589
rs753331181	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106723092	CATTGACTTCAATAT[A/G]AATTCACAATTTTAA	79589
rs753333499	snp	C/G	3.55379e-05	0.00421517	intron-variant, missense	RNF128	GRCh38.p7	X:106727092	ACACGGGAGTGAACC[C/G]TACGGTGTGGGAGCT	79589
rs753382735	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707879	GATGGCAACCTGAGT[A/G]TAAAACAGCAGATTG	79589
rs753428147	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706431	CTTATTCACTCAACA[A/G]ATGTTTACTGAGAGC	79589
rs753442150	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698741	AAGCCAAAGTGGCTT[C/T]TTAGAGAAAATAAAT	79589
rs753456117	snp	C/T	2.283e-05	0.00337853	synonymous-codon	RNF128	GRCh38.p7	X:106795629	TTCTGTGGCAGTGGA[C/T]GTTATTCCTCATGTT	79589
rs753477949	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106755048	AAGAAAAAGAGAAAA[C/T]CCAAATAGATAAAGA	79589
rs753498066	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106780404	GAGATTCTTCACTAA[C/T]TAGAGCGAATGCAGC	79589
rs753541993	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106786773	AGAATACAAACAACC[G/T]AATAGAAAACTGGCA	79589
rs753574614	snp	A/G	4.57582e-05	0.00478299	synonymous-codon	RNF128	GRCh38.p7	X:106790216	GACATGTGTTGACCC[A/G]TGGCTGTTAGAACAC	79589
rs753588997	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106727885	CTGTGCCCTGTTAAC[C/T]TCATTGCAATTTTGG	79589
rs753589442	in-del	-/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106738957	TAGAGCCTCTAATAT[-/G]GCAAAAGAAACCCTG	79589
rs753617760	in-del	-/AA			intron-variant	RNF128	GRCh38.p7	X:106710747	GGACGAAAGTCTGTC[-/AA]AAAAAAAAAAAAAAA	79589
rs753639969	in-del	-/TA			intron-variant	RNF128	GRCh38.p7	X:106729409	GTGATTATTAAGGAT[-/TA]TATATATATATACTA	79589
rs753642473	snp	C/T	0.000529661	0.016265	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726749	TGCATCTGCGGCAAC[C/T]TGTGTGCTGACGCTA	79589
rs753702369	snp	C/T	2.54013e-05	0.00356371	missense	RNF128	GRCh38.p7	X:106787994	TGGTACGCATCTTAA[C/T]GTGCAAGTAAGTTTG	79589
rs753737410	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106742226	ACATTACATACTGAG[A/G]AAAACAAAATAATTC	79589
rs753751376	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106717246	ATATTGTATTCAATA[C/T]GCAATGAAAAGTGAC	79589
rs753779285	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790563	TCTGTTTTTGTAATC[G/T]TTTACTATTGCATAG	79589
rs753808109	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106697938	CAAACATATATGTAT[A/G]TATACATATATTTTC	79589
rs753828605	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693728	ATAAGTTGACATGTA[A/G]AATAAAGTTGATGGT	79589
rs753834713	in-del	-/T	1.64757e-05	0.00287012	intron-variant	RNF128	GRCh38.p7	X:106790169	CAACTGATAATTATG[-/T]TTTTTTCCTGAATTA	79589
rs753858324	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765939	TGTTCTCATTGTTCA[A/G]TTCCCACCTATGAGT	79589
rs753873288	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730967	TGCCAATTAGTATTT[C/T]TTAAATCTTAGGCCA	79589
rs753904937	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791664	TCTCTGGAACCCATG[C/T]TTTGCAAGTAGGAAA	79589
rs753912285	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106729114	TACTTAGACCATTTT[C/T]CTTTTACTTCTGTTA	79589
rs753928789	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719302	TCAACTCACTTCAAC[A/C]TCCCCCACCCTGGGT	79589
rs753962892	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106751613	CAACTCCAGGCAGTA[C/G]AGCTCACAGCTCTGG	79589
rs753986803	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767128	CTGTAGCCTTGTAGT[A/G]TAGTTTGAAGTCAGG	79589
rs753987362	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106694666	TTTCCTCAGTGGGCA[G/T]TATATCGTGAGTTGC	79589
rs753988816	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106704981	AGGAGCTGGCAAGGG[A/C]AGAGCTGAACAGATT	79589
rs754038469	snp	A/G	2.28946e-05	0.00338331	missense	RNF128	GRCh38.p7	X:106772943	TTGCAATCATGATCG[A/G]CAATCTGAAAGGCAC	79589
rs754039283	snp	C/G	0.000140649	0.00838478	intron-variant	RNF128	GRCh38.p7	X:106785144	GAGACAAGGTACATT[C/G]ATGACTTTTAAATGC	79589
rs754051394	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106731131	AGCTACTATTATGTT[C/T]TAATCACAGTTAAAT	79589
rs754082208	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747405	TTTTCTTTGGGATGA[A/G]CGCTATGTTTGTTTA	79589
rs754087121	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720144	GGGGAGTAAAGACCA[C/T]TCATCTCCATAGTTC	79589
rs754089239	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710120	AAGCTAAACAGTAAA[A/G]TACCATGTTCTACTG	79589
rs754102545	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106714895	TAGCTCCTTTCTTTC[C/T]ATTGCTAAGTGATAT	79589
rs754113653	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106730831	AAAAAAAAAGTGAAT[A/G]AACCAAGCAGTTTAA	79589
rs754127155	snp	C/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106759531	ATGATTTGGAAGCAA[C/T]CTAAGTGTCCATCAA	79589
rs754162033	snp	A/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106714402	AAACTTTTTATTTTT[A/T]AAAAATGTAGATTTA	79589
rs754209164	in-del	-/A	0.0068637	0.0581785	intron-variant	RNF128	GRCh38.p7	X:106785884	AATCTTACCAAAGTC[-/A]TGAAACTGTAAAACA	79589
rs754235228	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750749	CACACAAAAAAAAAG[A/T]GAGAGAGGAGAGATG	79589
rs754235274	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106763994	TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC	79589
rs754237762	snp	C/T			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795843	CTCAGATGACTAATA[C/T]TATGCTATAGTTAAA	79589
rs754247570	in-del	-/TTGGT/TTGGTTTGGC			intron-variant	RNF128	GRCh38.p7	X:106763938	GTTTTTTGGTTTGGT[-/TTGGT/TTGGTTTGGC]TTGGTTTGGTTTGGT	79589
rs754262408	in-del	-/GA			intron-variant	RNF128	GRCh38.p7	X:106771518	TGCTGTGTTAGCAGT[-/GA]GAGCGAGGCTCCATG	79589
rs754293867	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106719684	TTTGTTAGGCTTTCA[A/T]CTAATGGAATATTAA	79589
rs754301683	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106704559	TACTGAAAATATCTG[A/C]AGGAGAAGTCGTGTC	79589
rs754319394	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106702698	ATATTCAGGTGCTAT[C/T]TTGATAAAGTTGGGG	79589
rs754328692	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106775775	ATTATCTCCATTTTA[A/C]TGGTAGAAATGATGA	79589
rs754344659	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106721058	CTAACTTGAGCTGAC[C/T]GAGGTTTAATCTTCA	79589
rs754387063	in-del	-/TAAT			intron-variant	RNF128	GRCh38.p7	X:106742843	ATGAATCAAAAAGAA[-/TAAT]TAATTTTATTAAATC	79589
rs754394573	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751763	ACATTTCTAGACACA[C/T]CCTGGGCCAGAAGGG	79589
rs754409707	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778540	ACACCTGGAAAAATG[A/G]ACCATGTTGTACCAG	79589
rs754431286	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787710	GTTCTGTTCCCCTTT[C/T]GTTTCAGTTTATTCT	79589
rs754461775	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106706505	CTGAAACTTCAAGCA[C/T]GCATGGCTTCTACCA	79589
rs754469115	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106715292	AATTTGCATTTCCCT[A/G]ATGGCTAATGACATT	79589
rs754495516	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106752111	AGCATTTCTAGACCC[A/G]CCCTGGGCCAGAAGG	79589
rs754513784	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106707929	GCAGTACAACACTGA[C/T]GGAGATCCAGGGACT	79589
rs754530651	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752930	TATACCGAAGAATGC[A/C]TCAGAGTCTTTCAAC	79589
rs754536259	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106786909	AATGAAATACAACTA[C/T]GCATTCATTAGAATG	79589
rs754585267	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732536	AATTCAATTCATCGA[G/T]CATTTATCAAAGGTC	79589
rs754640529	snp	A/C/G	0.000774649	0.0196675	intron-variant, missense	RNF128	GRCh38.p7	X:106726936	CGCCGCCTGGGGCCG[A/C/G]GGTCTCCTGCCGCGG	79589
rs754644343	snp	A/G	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106777057	TTCTGTGACATTTCC[A/G]GATTTTTTTTGTAAC	79589
rs754653464	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106696165	ACATTGAAAAAGATA[A/G]CATAATGATCATAAC	79589
rs754654235	snp	C/T	3.51766e-05	0.00419369	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727093	CACGGGAGTGAACCG[C/T]ACGGTGTGGGAGCTG	79589
rs754663796	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706298	CAAAACTGTGATTTT[C/T]GTAAATCTAAAAAAC	79589
rs754674545	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741920	AGCAGGACATCTAAC[A/G]CAGTCAGGTCAGAAT	79589
rs754693002	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767328	CATTTTCACAATATT[A/G]ATTCTTCCTATCCAT	79589
rs754709329	snp	A/G	2.28258e-05	0.00337822	missense	RNF128	GRCh38.p7	X:106795633	GTGGCAGTGGATGTT[A/G]TTCCTCATGTTGACA	79589
rs754732938	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699219	AAATGTAATTCCACC[C/T]CAGTTAGAATAAAAT	79589
rs754734053	snp	C/T	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106747368	CTCATCAGATACTTT[C/T]AGCAAATTAAGGACT	79589
rs754743562	in-del	-/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106705178	TCCAAATGGAACTGC[-/T]TTTATAGTCTTAATC	79589
rs754747640	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106759484	AGATGTCTACACCCC[C/T]GTGTTTATTGCAGCA	79589
rs754758518	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106766002	TGATAGTTTGCTCAG[A/G]ATGATGGTTTCTAGC	79589
rs754759836	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770632	CTCTACACTGTTTAT[C/T]CTAGTTAGCCATTCG	79589
rs754775118	snp	C/T	9.47261e-05	0.00688143	synonymous-codon	RNF128	GRCh38.p7	X:106694050	GCTCCTTGTAATTTT[C/T]ACCTTTTTACTTAAA	79589
rs754792313	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106696882	ATGGAAAACCACAGG[G/T]CATCCTACTAAGAGG	79589
rs754808399	snp	G/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106724898	GTCTTATTTGATTTT[G/T]CACCACAATGCTCAG	79589
rs754831983	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106710044	AACAAACACTCCAAT[A/G]TTCTAAATTTACTTT	79589
rs754863895	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770104	TTGTAGAGTTTCTGC[C/T]GAGAGATCCGCTGTT	79589
rs754955962	snp	C/T	2.36418e-05	0.00343807	intron-variant	RNF128	GRCh38.p7	X:106785159	CATGACTTTTAAATG[C/T]TATTTATTTTAAAGC	79589
rs754995855	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764149	TTTTTGTATTTTTAG[A/T]AGAGACGGGGTTTCA	79589
rs755000666	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699946	CATATTATTTTCTAT[A/C]AAAACCTTCAGGTCG	79589
rs755016576	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106776446	CAGATTAGAAGGAAA[C/T]CATCTTCCAAGAGGA	79589
rs755017807	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106731257	TAATTTGATCCCTTT[A/G]GGTACGGAGGGTAGA	79589
rs755035407	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106729140	TGTTAAGGGTATTTA[A/T]CTGATAGTTTTAGGA	79589
rs755088335	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106713482	CTGCACTCCAGCCTG[A/G]GCAACAGAGTGAGAC	79589
rs755116654	snp	A/G	6.84619e-05	0.00585032	synonymous-codon	RNF128	GRCh38.p7	X:106773088	TTTTATTATTACGGC[A/G]GCAACTGTGGGCTAT	79589
rs755122272	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693830	GGAATGTAGATAACT[A/G]AAGTGAAATAGAGCT	79589
rs755123916	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106789660	AGAAAAAAATAAAAT[A/G]AAATCATGCATCTGT	79589
rs755129449	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772416	TTGGGTTTGTAAACA[C/T]TGTTTGGCTCAAATT	79589
rs755145929	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106755533	AAATATTAACAAACC[A/G]AATTCAGCAACACAT	79589
rs755147500	in-del	C/TTTGTTTTTTTTTTT			intron-variant	RNF128	GRCh38.p7	X:106769543	GATTGCTACACCTGC[C/TTTGTTTTTTTTTTT]TTTTTTTGCTTTCCA	79589
rs755160358	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106792769	TCGATCATTGCACTT[-/A]ACTACACTGAGTTGT	79589
rs755165874	in-del	-/TGGGTATA	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106729442	CAGCTGATAATAGTC[-/TGGGTATA]ACTGAATGTTATAAT	79589
rs755197356	snp	C/G	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106754449	TTTTTTTTGTAGCGA[C/G]AGGGTCTCACCATAT	79589
rs755211985	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106714925	TTCCATGGTATAGAT[C/G]TACCACAGTTTGTTT	79589
rs755213860	snp	A/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106703923	ATAAAGTGGAATGGC[A/T]ACAAAAATTCCTGAA	79589
rs755224835	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106785218	ATGTTCTTCCTAAGT[A/G]TGCTTTTATTGGCAT	79589
rs755234321	in-del	-/TACT	0.00896606	0.0663524	intron-variant	RNF128	GRCh38.p7	X:106783449	AGACATTATACTAAA[-/TACT]TACATTATCTCTAAT	79589
rs755237340	snp	A/G	4.56595e-05	0.00477783	missense	RNF128	GRCh38.p7	X:106772957	GGCAATCTGAAAGGC[A/G]CAAAAATTCTGCAAT	79589
rs755263033	snp	A/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795963	CATTTTTAGACATTC[A/G]AAACTGTCTTCAAGA	79589
rs755308710	snp	C/T	0.00844089	0.0644143	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693371	AAGAAAACACACACA[C/T]ACACACACACACACA	79589
rs755317802	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106720732	CCCCACCACCTACCA[A/G]CTGTGTGACCTTCAG	79589
rs755326557	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106702708	GCTATTTTGATAAAG[C/T]TGGGGGAAAGATTTA	79589
rs755336562	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768324	CCTCTGGTAGACCTC[A/G]GCTGTGAATCCATCT	79589
rs755368112	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106719747	CAGTAGTATTACTAT[G/T]TTAGTTGAGAAAGAA	79589
rs755452011	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106704597	TAAGACGGGTTTTGG[C/T]TGAGTCAGGAAGCAC	79589
rs755460921	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106773331	CAAAGGTTTATTTTC[C/T]ATATTTGTCAAAGAA	79589
rs755461129	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106748222	AATCTATGTATTAGC[A/G]TATCAACATTGGTTT	79589
rs755492525	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749847	GAGGTGGAGACTGCA[A/G]TGAGCCGTGATCGTG	79589
rs755534907	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784248	GGATTTTTTCCTCTG[G/T]CTAGTTCACCATACA	79589
rs755546464	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106721596	TAGGATTTGAAGAAT[A/T]CAAAAAGGCTCCTGG	79589
rs755558070	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106721604	GAAGAATTCAAAAAG[G/T]CTCCTGGCCCATATA	79589
rs755558711	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768494	CTAGATTTTCTAGTT[C/T]ATTTGCGTAGAGGGG	79589
rs755575634	in-del	-/TTACTTGTTTT			intron-variant	RNF128	GRCh38.p7	X:106736238	CTCATTTAAATTGAG[-/TTACTTGTTTT]TAAAATGAGCATTTC	79589
rs755591676	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777777	GAGTTCCAGACCAAC[C/T]TGTGCAACATGGCAA	79589
rs755609097	in-del	-/AAAAAAAAAC	0.000607533	0.0174183	intron-variant	RNF128	GRCh38.p7	X:106706387	ATGCTTCCTTATGTG[-/AAAAAAAAAC]AAAAAAAAACAAGGG	79589
rs755683564	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106722868	CTCGGTGAGGATGAA[C/T]TCAGAGCAAGGGGGG	79589
rs755696931	snp	C/T	0.000245791	0.0110831	intron-variant, missense	RNF128	GRCh38.p7	X:106726926	GCCATGGGGCCGCCG[C/T]CTGGGGCCGGGGTCT	79589
rs755734798	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106706320	CTAAAAAACAATGTG[C/G]ATTTGTTTATACACA	79589
rs755793684	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769245	CTGCTTGGTGCAGCG[A/C]TAAGTTCAGTTCCTG	79589
rs755815087	snp	A/G	0.00033868	0.0130087	missense	RNF128	GRCh38.p7	X:106787973	AATTGTATAAACCAA[A/G]TGATTTGGTACGCAT	79589
rs755815671	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106776165	TTATGGCATACACAA[A/G]TTAAACTACATTCAG	79589
rs755819851	snp	A/C	0.00015246	0.00872966	intron-variant	RNF128	GRCh38.p7	X:106694415	CAAATTTTGGTAAGT[A/C]ATAATTGATTCACAA	79589
rs755865531	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106762675	GGTTTGTTGTATAGG[C/T]AAATTGTGTGTCACA	79589
rs755868837	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106784911	TTATATCAGGTAAAT[A/G]GGACATTTATTATGG	79589
rs755873220	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106777943	CCACTGCTCTCCAGC[C/T]TGGGTGACAGTGAGA	79589
rs755877966	snp	C/T	0.00317376	0.039709	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725052	TGTTTCTTCAAAGTA[C/T]AATATAGTTGGCTGT	79589
rs755891244	in-del	-/AC			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693362	GAGCCTGCTAAGAAA[-/AC]ACACACACACACACA	79589
rs755893104	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787047	ATGTTTGGCAGTTCC[-/T]TATGAAGTTAAAAAT	79589
rs755916929	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106738908	TCTATAGCCCAGCTT[G/T]GGAGATTGGCAGTGT	79589
rs755918987	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106764391	AAAACTTATGGCCAG[G/T]TGCAGTGGCTGACGC	79589
rs755921274	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764992	ATTATCTCCAGATCC[A/G]TAAGGGATATTTGGG	79589
rs755942887	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106712703	AAGTTAAGTAAAAGG[G/T]TTATTTTAATAACCC	79589
rs755975162	in-del	-/GT			intron-variant	RNF128	GRCh38.p7	X:106708310	CCTAGGTTACCAACA[-/GT]GATTCACACAGCTAC	79589
rs755976265	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771654	AGGTACGGTCTGTCA[C/T]GGCTTCCCTTTGCTA	79589
rs756007610	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765783	CAGGTTTGTCACATA[A/T]GTTTACATGTGCCAT	79589
rs756057483	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106696688	CTCTGGCTCCCCCTA[C/T]CTCTTCATTCCTTCA	79589
rs756063323	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106754099	AGTAGAGAACAAATG[A/G]ACCTAATAGATATTT	79589
rs756086214	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790917	TGACTGGGGCTAACA[A/C]GAGACTTGTGATCAT	79589
rs756113894	in-del	-/AAATTC	2.31241e-05	0.00340022	cds-indel	RNF128	GRCh38.p7	X:106694316	GTACATTTTCAGAAA[-/AAATTC]AAACAGCGGGCAGAA	79589
rs756115006	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106740450	CCCAGTTTCATTGTA[A/T]GTCTAGGCTATGACC	79589
rs756130706	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766485	ATGAACATTTTTTCA[C/T]GTGTCTTTTGGCTGC	79589
rs756135713	snp	C/T			downstream-variant-500B	RNF128	GRCh38.p7	X:106797339	ATCATTCATGAGGGA[C/T]CCACCTTCATGATCC	79589
rs756140770	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715351	TCTGTATTTCCTCTT[C/T]GGTGAAATGTTTATT	79589
rs756149422	snp	C/G	4.59733e-05	0.00479422	intron-variant, missense	RNF128	GRCh38.p7	X:106727343	GGGGCGTCTGGAGCC[C/G]TCATCTTTAACTTCC	79589
rs756155301	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106749945	ATGCACAAGTGAAAA[G/T]AATAGCAAAGTAAAA	79589
rs756173473	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106747993	ATTCAGTAAAACACT[C/T]AATGAATGAAATTAA	79589
rs756219332	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704326	TAGTCCCAGCTACTC[C/G]GGAGGCTGAGGTAGG	79589
rs756233148	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708637	AGCAACTGTTTTCTG[C/T]AAACAATCTTTGCCT	79589
rs756248957	snp	C/T	2.7182e-05	0.0036865	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693954	AATGGTGACTGATAG[C/T]TGGAAATATCAGCAA	79589
rs756257109	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106766118	TCCAGTCTATTATTG[A/T]AGGACATTTGGGTTG	79589
rs756299393	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774344	GATGAACTGTTCCTT[A/T]GCAAAGGCTAACTCT	79589
rs756302792	snp	A/C	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106791601	ATAAAGGAGTTCTGA[A/C]ATGATAAAACAGAAT	79589
rs756316767	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106780903	TGGATATTAAAATAG[C/T]TATTTCACAATGTTG	79589
rs756344576	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719259	AACAGAGTCTCTGTT[C/G]CCCTGGCTGGAGTGC	79589
rs756347605	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106783492	ACATAAATGTCAGCT[C/G]GGGACGGGGGTACAT	79589
rs756427152	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749911	CCTTGTTTCAAAAAA[A/C]AAAAAAAGGAAATTA	79589
rs756429632	snp	C/T	2.4131e-05	0.00347346	intron-variant	RNF128	GRCh38.p7	X:106791276	GTGCCCTGCAATCCA[C/T]TGTAGATCATATGCC	79589
rs756464893	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711376	TCATAAAACACAGGA[A/G]AGTTCCTAAGCACAT	79589
rs756464915	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106728727	CTTCTTTGCCTCTAC[C/T]GACTTTGTAACCTTG	79589
rs756473158	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106718317	AATTTCTGCCCTCTT[A/T]TTCCCCCTCTCGAAA	79589
rs756479766	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716502	AAACCATTCTATATC[C/T]TGACTGTGATGGTAG	79589
rs756492880	snp	G/T	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106712701	AAAAGTTAAGTAAAA[G/T]GGTTATTTTAATAAC	79589
rs756495702	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106736306	ATTCCACTAGTTGGT[A/G]GTTTATACAAGAAAC	79589
rs756504896	snp	A/G	0.00158814	0.0281345	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796276	TATTTTTAAAATTAG[A/G]CTGAATGTACTTCAT	79589
rs756515596	in-del	-/T	0.177827	0.239355	intron-variant	RNF128	GRCh38.p7	X:106762317	ATTCTCCACTTTTGA[-/T]TTTTTTTTTTTTTTT	79589
rs756588947	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106793848	GATGTTGGTGTCTTA[C/T]TAGTGATGATTCAAA	79589
rs756594947	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739134	TCCTTCCTTCCTTTT[C/T]TCCTTCCTTCCTTCC	79589
rs756601722	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106784365	CTTCTGACTCAATTA[C/T]GCATAATGTTTTAGT	79589
rs756653008	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728241	TAAAGGACAAAGGGG[-/A]AAAAAATGGAGAAAA	79589
rs756654202	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750633	ACAGAGGGTACTTGC[C/T]CTGAAGCCCCCAAGC	79589
rs756669368	in-del	-/AA			intron-variant	RNF128	GRCh38.p7	X:106745290	TTAAAAAATGGTAAT[-/AA]AAAGGTGATTTGGGT	79589
rs756672086	snp	A/T	2.50595e-05	0.00353965	missense	RNF128	GRCh38.p7	X:106694402	ACGATACAGATGGCA[A/T]ATTTTGGTAAGTAAT	79589
rs756688592	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106771252	CAGATCTCAAACTCC[A/G]TGCTGGGAGAACCAC	79589
rs756706411	in-del	-/GTA	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106773287	GTTTTACAAAATCTG[-/GTA]GTTTTTAAAAGTATG	79589
rs756715130	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106694664	AGTTTCCTCAGTGGG[C/T]ATTATATCGTGAGTT	79589
rs756722645	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106720079	AAAGGAAAGATAGGA[C/G]ACTGCATGAGACAAG	79589
rs756750058	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106762351	ATGGAGTTTTGCTCT[C/T]GTTGCCCAGGCTGGA	79589
rs756751415	in-del	-/TTTGA			intron-variant	RNF128	GRCh38.p7	X:106763937	TGTTTTTTGGTTTGG[-/TTTGA]TTTGGTTTGGTTTGG	79589
rs756759809	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769319	GACAGTGGGGTTTTA[A/T]AGTCTCCCATTATTA	79589
rs756779416	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769972	TCTCTCAGCATTTGT[C/T]TGTCTGTAAAGAATT	79589
rs756795176	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708449	TTATCTACATAAGCT[A/G]TTGTAGATGTAGTGA	79589
rs756797623	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106740131	TGCTGAATGTTGTAG[C/T]AGGAGAAGGGGAGTG	79589
rs756804506	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106734078	ACTAGTTTTGTATAC[A/T]GCTTTCTATTGTAAG	79589
rs756856646	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106750771	GGAGAGATGCTGCTA[A/G]AAGCAACAACTGAAG	79589
rs756881027	in-del	-/TG			intron-variant	RNF128	GRCh38.p7	X:106696020	ATAATCATTTGAATA[-/TG]TGACTCTGAACAGAG	79589
rs756895567	snp	C/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796825	TTGTTTTAGAATTTT[C/G]TTCAAATTATAGCAG	79589
rs756904111	snp	A/C			downstream-variant-500B	RNF128	GRCh38.p7	X:106797094	AAGGAAAACAGGATT[A/C]ATTGGCTCATGGTTT	79589
rs756911714	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750168	CCAATTCCACATTCA[C/G]GTGGCTATGGTGGGA	79589
rs756953772	snp	C/G	2.29024e-05	0.00338389	synonymous-codon	RNF128	GRCh38.p7	X:106790264	CAAATGTGACATACT[C/G]AAAGCTTTGGGAATT	79589
rs756981585	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106773742	TAACAGTGTATAAAA[A/T]GGTACAAGGTACACA	79589
rs756982923	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106708355	ACCCACACAGGGTTA[C/T]GGAGTGAAGGAAACA	79589
rs757010140	snp	A/G/T	0.00211738	0.0324783	intron-variant	RNF128	GRCh38.p7	X:106777285	ATTAAATTGCTCTGT[A/G/T]CAAGTCTATCACAAA	79589
rs757033111	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106703102	GTAGTTAAGTGAATT[C/T]GTCTCTAGCAATAAT	79589
rs757033338	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722713	ACGAGAGACCAATAT[A/G]TAAGCCAGAATGCCA	79589
rs757038390	in-del	-/T	0.000152528	0.0087316	frameshift-variant	RNF128	GRCh38.p7	X:106694026	GGAGAATAGGTCCAG[-/T]TTTTTTTGGCTCCTT	79589
rs757061251	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789515	TATAGTGTATATATT[A/C]TATACATTATACACT	79589
rs757064735	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716222	TTCCTGCCTCTATTC[C/T]AGCACAGGACTTTGT	79589
rs757074051	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754165	ATTGTCTCTTTGGCA[C/T]GTGGATCATTCTCAA	79589
rs757096408	snp	A/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106727998	CTTCTGAAAAATCTG[A/T]TTTAGGTTATTGAGT	79589
rs757100105	snp	A/C	6.97885e-05	0.00590672	intron-variant, missense	RNF128	GRCh38.p7	X:106726947	GCCGGGGTCTCCTGC[A/C]GCGGTGGCTGCGGCT	79589
rs757101071	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106744665	GGGGTTTCACCGTGT[C/T]AACCAGGATGGTCTC	79589
rs757109011	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711154	TAGGAAGATGTGCTT[A/G]TTTATAGGAGCCAGC	79589
rs757146268	in-del	-/A			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796389	CAAAAAATTCCTTAC[-/A]AAAAATACTGTGTAA	79589
rs757165102	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106783224	AAATATCTTCCACAA[A/G]ATGATATCTTATATA	79589
rs757173287	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106760978	CTATCAACAGAGTAA[A/G]CAGACAACCTACAGA	79589
rs757186030	in-del	-/C	0.000147078	0.00857424	intron-variant	RNF128	GRCh38.p7	X:106788046	AAAATAGCTGACCCA[-/C]AAAAATGACTGTGAT	79589
rs757216942	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733500	AGTGTAAAACTAAAA[A/T]ACCCATAATTCTACA	79589
rs757222432	snp	A/C	0.0100156	0.0700533	intron-variant	RNF128	GRCh38.p7	X:106706397	ATGTGAAAAAAAAAC[A/C]AAAAAAAACAAGGGT	79589
rs757222498	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717250	TGTATTCAATATGCA[A/G]TGAAAAGTGACATAA	79589
rs757224557	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106762538	AGCTGGTCTTGAACT[C/G]CTGACCTCAGGTGAT	79589
rs757229587	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106743384	TCACCATATAACTGC[A/G]TAACTCAGTGAATCT	79589
rs757271449	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106793052	CTAAGTTCTATTAGA[C/G]CACTGGTTTTCAAAC	79589
rs757283071	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759585	TGGTACTTACACACA[A/G]TGGAGTACTATTCAG	79589
rs757296139	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106717540	CTTAATTTAACTTGT[C/T]GCATTCATGTTTTTA	79589
rs757319664	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106769078	GCACTGTGATCTGAG[A/G]CAGTTTGTTATAATT	79589
rs757356572	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106695716	AATGCCATTTTCTGA[C/T]AAAACTTAGGAATTA	79589
rs757395794	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791668	TGGAACCCATGTTTT[A/G]CAAGTAGGAAACTGT	79589
rs757403303	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758239	AAGAAGAGAGCTCTA[A/C]AATGAAAACTGTAAA	79589
rs757426879	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106745764	ACTGAGACCAATCAA[A/G]AGGAAACAAAAAAAG	79589
rs757430922	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719356	CTCTCGAGTACCTGG[A/G]ATTACAGGTGTGCTC	79589
rs757441665	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770685	TACTTCTTTGCGATG[A/G]GTTCGAACATCCTCC	79589
rs757491601	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783087	CCTTTTTAGGGTCTA[C/G]GCCTTCCTATTCACT	79589
rs757537473	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711075	ACAGCAAATATAAAA[A/G]TAATTTTTGCTAAAA	79589
rs757540590	in-del	-/GA	0.000190628	0.00976103	intron-variant	RNF128	GRCh38.p7	X:106795537	TTTGTCTTAAAAGAG[-/GA]GAGGGGCAAAATCAT	79589
rs757590862	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710224	TGTCTTTGATATACC[A/C]CTAGAATTTGTTTTG	79589
rs757595918	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106732192	AAATGCAACACAAAT[A/G]CCTCCTCATCTTTGA	79589
rs757619588	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106747816	ACTACTGGCCATAAT[A/G]GTAGATATATACAAT	79589
rs757623430	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725807	CATAACTATCAGACA[A/G]CAGGTATATTAATTC	79589
rs757631142	snp	G/T	2.42574e-05	0.00348255	intron-variant	RNF128	GRCh38.p7	X:106772898	AACTAAAACTGAATT[G/T]GTTTTATTTTACAGG	79589
rs757637702	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774423	CACTCCAGAAATTTT[C/T]CTCTCTCACTCTCCT	79589
rs757675118	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106787362	AAAGCTAGATAATGC[A/G]TGATTCCATTTATAT	79589
rs757712330	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730995	CCAGTTATTTTACTT[C/T]TCTAAGTCTCAGTTT	79589
rs757733363	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106694695	GCTTTTTAATAAACT[C/G]TGCCTTTACCTCTAA	79589
rs757741595	snp	A/G	4.77048e-05	0.00488366	intron-variant	RNF128	GRCh38.p7	X:106791053	CTTTTAATTTGTTAC[A/G]TGTTCTTTAAAGGTG	79589
rs757755090	in-del	-/AG			intron-variant	RNF128	GRCh38.p7	X:106771582	ATCTCCTGGTGTGCC[-/AG]ATTTGCTAAGGCTGT	79589
rs757757655	snp	A/G	2.31104e-05	0.00339922	intron-variant, missense	RNF128	GRCh38.p7	X:106727301	GGCTGCACCTTCGCA[A/G]ACAAGATCCATCTGG	79589
rs757762558	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106773454	AATAAACATTTTTTT[C/T]TAAATTACAAAAACA	79589
rs757766914	snp	C/T	0.0142023	0.083063	intron-variant	RNF128	GRCh38.p7	X:106704381	GAGCTTGCAGTGAGC[C/T]GAGATCGCGCCACGC	79589
rs757772512	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106718608	TCTGATTCAATGCAT[C/G]TGGGCTTTTTTTTCC	79589
rs757809113	snp	A/G	3.04326e-05	0.00390069	intron-variant, missense	RNF128	GRCh38.p7	X:106727160	GAGCCTGTGGCTGGG[A/G]TCCTGGTACCGCCCG	79589
rs757816968	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106740637	TGCAGTGGTGCAATC[A/G]TAGTTCACTGCAGCC	79589
rs757842848	snp	A/G	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106750820	AAAGAAAATTATCCA[A/G]TGTGAGAACTCAAAA	79589
rs757845546	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786003	TCGGTTCCCCACCAA[A/G]CTAATTTATGGATTT	79589
rs757857920	in-del	-/C			intron-variant	RNF128	GRCh38.p7	X:106713172	GATTACAGGTGTGAG[-/C]CGCTGTCCCCAGCCC	79589
rs757866929	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766595	ATTTGTTCAAGTTCA[G/T]TGTAGATTCTGGATA	79589
rs757870059	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106710469	CAGGGATACGAAAAG[C/T]TGATCTGGCTGGGCA	79589
rs757922904	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764119	AGGTGCCCGCCACCA[C/T]GCCCGACTAATTTTT	79589
rs757929692	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692784	CCAGATTACCTGACT[C/T]GGACCTTGGACTACC	79589
rs757933869	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699782	AACCACTCTGATCTT[C/T]GGACATTTTCTCCAA	79589
rs757954881	in-del	-/ATG			intron-variant	RNF128	GRCh38.p7	X:106730850	CAAGCAGTTTAATTA[-/ATG]ATTTGGGGGTCTCCA	79589
rs757961745	snp	A/G	3.3036e-05	0.0040641	intron-variant	RNF128	GRCh38.p7	X:106788020	GTTTGATTTTCTTCT[A/G]TATCTTCAATAAAAT	79589
rs757962818	in-del	-/TATG	0.00633741	0.0559334	intron-variant	RNF128	GRCh38.p7	X:106723582	AAATATATATATATA[-/TATG]TATGTATGTATGTAT	79589
rs758016961	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704400	ATCGCGCCACGCACT[A/C]CAGCCTGGGCGACAG	79589
rs758034229	snp	A/C	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106770546	TGATCAAATCGGCTA[A/C]TGAAGCTTGTGCATG	79589
rs758069162	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715170	CAAAAAAAAATGTAC[A/G]TATGATCCAGCTTCT	79589
rs758075864	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106723792	TGCTTGGGTCACTCC[A/T]TTTGTACTTAAAGAC	79589
rs758094477	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774694	AAGCCACCATAATTT[A/C]TTACCTCCTCCTCCC	79589
rs758162206	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106745226	TCTAGAGGTGCAGGG[A/C]AGAAAGGCAACTTGC	79589
rs758180655	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106744758	GCCACCAAGCCCAGC[C/T]GAATAAATAAATAAA	79589
rs758191460	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106718499	CCAAAGCTACACAGA[A/G]ACAGCTTAGAAAAAA	79589
rs758282202	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106745816	AAGAAAGAGAGGCTA[A/G]TTTGGCTTAAAAGTT	79589
rs758307925	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796711	TGAAAAAGAAGGGGG[A/G]GAGAATTCCAGGTGC	79589
rs758328376	snp	C/G	2.28511e-05	0.0033801	missense	RNF128	GRCh38.p7	X:106694270	AGTAATACTAAGAAG[C/G]CCTGGATTGCGCTGA	79589
rs758328994	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106780562	GGAGGAGGGGAAAGG[C/T]AAAAGGCGTTTGACA	79589
rs758336782	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106778648	ACATGGCCAGTTGCT[A/G]GCAGGATGCACCTAG	79589
rs758348080	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106778656	AGTTGCTAGCAGGAT[G/T]CACCTAGTAAGCAGT	79589
rs758353599	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784123	TTCATATGTATATTA[C/T]ATTCACTTGAGGCAT	79589
rs758373337	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708600	CTTTCAGAGAAAGAA[A/G]CTCTTTTAAGTAGTA	79589
rs758407763	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106755484	ACTACTACAGGCAAG[A/T]CTCTCTGATGAACAT	79589
rs758416725	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771712	CTTCCTGGGTGAGGC[A/G]ATGGCCTGCCCTGCT	79589
rs758445640	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106770055	TTGAAAATTCTTTAA[A/G]AATGTTGAATATTGG	79589
rs758453278	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106733982	CTGGAATTACAGGCG[C/T]GAGCCACAGTGCCCA	79589
rs758471424	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106737101	ACTACATTTTGTTTT[C/T]TTAATCTTTGAGGAT	79589
rs758479148	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106715200	TCCACATCCTTAACA[A/G]CATTTGGTGTAGACA	79589
rs758487225	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106698088	CCGAGCACTGCAGAC[A/G]TGGCCTTTCAGTTCT	79589
rs758508447	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106716251	GTACTCCCTCACAGC[A/G]CTTATCTCTCTGACC	79589
rs758515179	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106787155	ACACAACTGTTCATA[A/G]CAGCTTTATTCATAA	79589
rs758522829	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106783982	ACGCCCCACCTCCAA[-/T]CATTGGGGGTCACAC	79589
rs758523157	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106748667	ATGAAATAAGCAAGG[A/C]ACAGAAAGACAAATG	79589
rs758530694	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711202	CACCGCCTAGCCCCA[A/T]GGGAGTGGAGGGTTG	79589
rs758540726	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106697038	TTAATGTTAAACCAG[C/G]AAATTCCTGGGAAAA	79589
rs758542218	snp	A/G	6.94067e-05	0.00589055	missense	RNF128	GRCh38.p7	X:106785095	GATGCTAAAAAAGCT[A/G]TTGGAAGGCTTCAAC	79589
rs758549676	in-del	-/C	2.31e-05	0.00339845	intron-variant	RNF128	GRCh38.p7	X:106790176	TAATTATGTTTTTTT[-/C]CTGAATTAGCCATAT	79589
rs758582729	in-del	-/C	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106765068	TCAGACTCCTTCACT[-/C]CCCCATTGTTTTTGA	79589
rs758588549	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106742580	AAATTATGATCTGGG[G/T]ACTACTAGTCTCTGA	79589
rs758590783	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106712236	TTTTATTATCTGCTC[C/T]TTTGTATCATCTGCA	79589
rs758649885	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106775929	CCATAAATTCTGATG[A/G]CTGAATGCTCAGATG	79589
rs758650708	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772378	GAAAAATGGTACATC[A/G]TGGACATATGTAGTT	79589
rs758669244	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702566	TACCCCAGCTACCTC[C/T]CTTCCTTCATTCGAA	79589
rs758676769	snp	G/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106767208	ATGCGGGCTCTTTGG[G/T]TTCCATATGAACTTT	79589
rs758677651	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106766217	ATGATTTATAATCCT[A/T]TGGGTATATGCCCAG	79589
rs758681489	in-del	-/TT			intron-variant	RNF128	GRCh38.p7	X:106773743	ACAGTGTATAAAAAG[-/TT]GTACAAGGTACACAA	79589
rs758692763	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705153	AATATAAAACTAACC[C/T]GCCCTAGGTTTCCAA	79589
rs758694278	snp	C/T	4.57959e-05	0.00478496	missense	RNF128	GRCh38.p7	X:106773131	TCTGCTCGAAGGCTA[C/T]GGAATGCAAGAGCTC	79589
rs758696918	snp	A/G	3.37838e-05	0.00410984	intron-variant, missense	RNF128	GRCh38.p7	X:106727121	CTGAGCGAGGAGGGC[A/G]TGTACGGCCAGGACT	79589
rs758722160	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106750420	CACTTACTAGCTTGT[G/T]TTACCCTAGGCAGTT	79589
rs758731694	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775880	TGAAGGTTATGATAC[A/G]TGGTATATAATGTCA	79589
rs758732799	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106768164	TCATCAGGGATTTTC[A/G]TCTAAAATTTTCTTT	79589
rs758738374	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731226	AGTACTTCAAAGTCC[A/G]CATTACCTGAAATTC	79589
rs758757212	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106701717	GTTGTAAGACACAAA[C/T]AAACAGTAAAAGCAT	79589
rs758790541	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106694874	GTTATAGAAATGAGA[A/G]CTTGACTCTACTGTA	79589
rs758808393	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106704911	ATCAATGTAAAGGGC[C/T]GGCATTGTATATGAA	79589
rs758837788	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766673	GTAGGTTGCCTGTTC[A/G]CTCTGACGGTAGTTT	79589
rs758876274	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106720405	GTTTTGTAGAGACAG[A/G]ATCTCGCTATGTTGC	79589
rs758892089	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719499	GTGCTGGGATTACAG[A/G]GGTGAGCCACTGCAC	79589
rs758895951	snp	C/T	2.2823e-05	0.00337801	synonymous-codon	RNF128	GRCh38.p7	X:106795641	GGATGTTATTCCTCA[C/T]GTTGACAACCCAACC	79589
rs758928310	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747533	AGAAACCTAGCACAG[A/C]CTGACCTCCTTCATG	79589
rs758979309	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759630	GAGTTCCTGTCATTT[G/T]CAACAACACATATGG	79589
rs758989599	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106785342	CTGTGCATATTACCT[C/T]ATATGGCAAAAAGGA	79589
rs759036898	in-del	-/TA			intron-variant	RNF128	GRCh38.p7	X:106729410	GATTATTAAGGATTA[-/TA]TATATATATATACTA	79589
rs759049586	snp	C/T	1.648e-05	0.0028705	intron-variant	RNF128	GRCh38.p7	X:106727431	TTGCACCCCTCCAGA[C/T]CTCTGCCATGGCCAG	79589
rs759065473	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106738813	GGGTTATTGTGAGGT[A/G]TAAATTAAATAATAT	79589
rs759073755	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726486	CCAGAAAGCTTTATG[C/T]TTGCGGACTTTATCG	79589
rs759095195	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716868	AGGAGGAAGTGGTCA[A/G]ATTGACTTAGATTGT	79589
rs759104711	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106780446	CAGAATAGTCACATT[A/G]AGCTTCTGTTAAGAA	79589
rs759110955	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702362	CTCCTAAATTTTTAA[C/T]GTTTCATTTATTATG	79589
rs759111259	snp	A/C	2.3553e-05	0.00343161	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795729	AATCTGTGTAAATAG[A/C]AAACTTGAACCATTA	79589
rs759128696	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106709967	TAGGGAAAGAAAATA[G/T]TACTCAGAAGAGAAG	79589
rs759146300	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789106	TAGTATATATATACT[A/G]TATACTATATATACT	79589
rs759148405	snp	A/G	7.00664e-05	0.00591847	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727276	GTTGGCCCTCATCCA[A/G]CGCGGCGGGGGCTGC	79589
rs759178027	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693542	TTTCAGCAGGGCTTG[A/G]CAAACCAGTTTAGTG	79589
rs759192549	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783036	ACAATTATGTCCCAA[A/G]ATGGGAGTGAAAGTG	79589
rs759218182	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106735306	TTAACCCTATTCATT[C/T]TGACCTTTTTTGAAA	79589
rs759219537	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754737	TAAAATTTCTTGAAA[C/T]AAGTGGAAATGAAAA	79589
rs759261036	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106767997	TTTATCTTTGGTTCT[C/G]TTTATATGATGGATT	79589
rs759261711	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794021	TACTTTTAGCAATCA[C/T]TGATGCTTCTTGCTT	79589
rs759267543	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716968	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	79589
rs759272490	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106753877	ATTATATAATGATAA[A/G]AGGATCAATTCAGCA	79589
rs759282079	snp	C/T	2.4173e-05	0.00347648	intron-variant	RNF128	GRCh38.p7	X:106791022	TATGTCGAGGAAAAG[C/T]GTGTACACTGAGAGG	79589
rs759331145	snp	A/G	2.28723e-05	0.00338166	missense	RNF128	GRCh38.p7	X:106790230	CATGGCTGTTAGAAC[A/G]CAGGACTTGCCCCAT	79589
rs759340155	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106789759	TTTAGCTATTTAATA[C/T]AATAGTGATGCTCTT	79589
rs759342343	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716114	TGAAATACCTTCCCT[C/T]ACCATTTGTGTCCAT	79589
rs759386494	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106792951	GTTTAAGAATCTTGC[A/G]TATTAGCCATTGATT	79589
rs759429884	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106698059	GTAAGTATGTAACTT[C/G]CTAACAATCTTTTCC	79589
rs759438993	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710867	TCTCTCTAGGTTTAG[A/T]CTAGCTTCATGATTT	79589
rs759455301	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106744999	GATCAGGTGTTTTAT[A/G]TAATATTTCTAAGAA	79589
rs759471541	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106738116	GTGTTCCATTTGAAA[-/T]TTGGGGGACAGCATA	79589
rs759483226	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106699161	TTCTCTCTTGCTATT[C/T]TCGCCCCTCTGTAGC	79589
rs759502198	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106750548	TATCTGGCAACCTCA[A/G]AAATCCAGTGCATAG	79589
rs759508739	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106791006	AGAAACTTTGAAGTG[A/T]TATGTCGAGGAAAAG	79589
rs759510108	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106712077	TGGCTAGCCCACCGG[G/T]GGTGGTTAAATCTCA	79589
rs759523386	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106748029	CTGTCTGTCTTCTGT[A/G]TAACCGGTCCACAAG	79589
rs759562080	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106777465	TGTGTTGTTCTTATG[A/G]CACCTTATATAAAAA	79589
rs759578277	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784916	TCAGGTAAATGGGAC[A/G]TTTATTATGGCTAAT	79589
rs759581808	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106770386	TTCAGGTACACCAAT[C/G]AGACGTAGATTTGGT	79589
rs759591472	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106721108	TATTTGGAAGTATGC[C/T]GTTGGCATCATGCTT	79589
rs759598207	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785554	GGAGCTAAGGGATGC[A/G]GACAGCCTCTAGAAG	79589
rs759615596	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106753548	AGAGAGGGAACAAAG[G/T]AAGAGATCACAAAAC	79589
rs759641816	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723307	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	79589
rs759642668	snp	A/T	2.33478e-05	0.00341663	intron-variant	RNF128	GRCh38.p7	X:106785061	GCTGTTTTTTTTTTT[A/T]CAGAGGCAATTAAAG	79589
rs759741760	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106707102	TGTATTCTTATGTAT[G/T]CATTTGTATAATTCC	79589
rs759773263	snp	A/T	0.0110639	0.0735497	intron-variant	RNF128	GRCh38.p7	X:106704295	CAAAAAAGCCAGGCG[A/T]GGTGGCTGGCGCCTG	79589
rs759781388	snp	A/G	9.06372e-05	0.0067313	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106726973	CGGCTTTTCCAGATT[A/G]CTGGCATGGTGCTTC	79589
rs759856939	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106733513	AATACCCATAATTCT[A/G]CAACACAGATGACAC	79589
rs759857147	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751429	CCATCCCTCTGGCAA[G/T]CCTCACCACTGTGAG	79589
rs759877180	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106696263	ACATTGTTTTTTAAC[A/G]TATGATGATATCAAC	79589
rs759899064	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735138	CCGATAGTCTTAGTG[C/T]AATATTGATTTATTT	79589
rs759926574	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106744457	ATTACTTTAACATGA[A/G]CTTATGATTATTTTA	79589
rs759928589	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769133	AGTGTTTTACTTCCA[A/C]CTATGTCGTCCATTT	79589
rs759930078	snp	A/T	0.00791544	0.0624105	intron-variant	RNF128	GRCh38.p7	X:106777731	TACCAGCACTTTGGG[A/T]GGCCGAGGCGGGTGG	79589
rs759948977	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717701	GCCCAATGATAGTTA[C/T]TGCTTACAATTTTAT	79589
rs759979360	in-del	-/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106722551	GGTAAAACCAGTGGG[-/T]TACCCAGGCAAGTCT	79589
rs759982392	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706990	AGAAGTCTTTTTTGG[C/T]TAACAGTTTATCCTG	79589
rs759996222	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790288	GGGAATTGAGGTAAA[C/T]ATTAATATGTTATTT	79589
rs760008669	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106721199	TGCTATCTACATAGA[A/G]CAGCTGCCTGGAGTG	79589
rs760008800	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106741927	CATCTAACGCAGTCA[A/G]GTCAGAATCTTATAA	79589
rs760036525	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769792	TTTGATCCTGTCATT[A/G]TGATGTTAGCTGGTT	79589
rs760037850	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790463	ATCTCCATTTTCCTT[C/T]TTCCTCCCTCTTTCC	79589
rs760059821	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106722432	TGCATTTCTAACCAG[C/T]TCCCTGATGATGCTG	79589
rs760073216	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106775496	TAATTAACCTCTGTA[A/G]AAATGGTCAAGAATA	79589
rs760076748	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766195	GTGCATGTGTCTTTA[A/T]AGCAGCATGATTTAT	79589
rs760086444	snp	A/T	4.98126e-05	0.00499037	intron-variant	RNF128	GRCh38.p7	X:106787884	AATGTATTTTTTCTT[A/T]TCTGTCAGAGTAACA	79589
rs760147738	snp	A/C	0.000529661	0.016265	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795773	TGCCAATCAGGGCCT[A/C]GTTTCTATTAATAAA	79589
rs760159213	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106742143	ATGGTGACAATGGAG[A/T]TATAATATAACAGGA	79589
rs760189195	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725174	CCTACCCATTTTTCC[C/T]CTAGGTAATTTTTAT	79589
rs760208055	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728537	TTAGCTGATAGGATT[A/T]GCCTTCTGGGAGTCA	79589
rs760209041	in-del	-/AG			intron-variant	RNF128	GRCh38.p7	X:106770926	TGGTGACGTACTGAC[-/AG]GGTTTTGGTGTGGAT	79589
rs760214509	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106767697	TTTTCCTAATTGAAT[A/G]CTCTTTATTTCCTTC	79589
rs760217253	snp	A/G	3.30426e-05	0.0040645	intron-variant, missense	RNF128	GRCh38.p7	X:106727068	TCAACGTGTCCTGGC[A/G]GGTTCCGCACACGGG	79589
rs760222144	snp	A/G	3.30967e-05	0.00406783	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693979	CAGCAAACATCTTAA[A/G]TTTTATACTCAAATG	79589
rs760235624	in-del	-/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106754951	AGAAATAAATTGAAA[-/T]AAAAAAACACAAAAC	79589
rs760236256	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106708141	AAGATTGGGGTTCCT[C/T]GGCTTGATGACACCA	79589
rs760259757	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717209	CTCCGTCTCAAAAAA[A/C]AAAAAAGAAAGAAAG	79589
rs760313279	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106698985	AAGTAACCCCTGATG[C/G]CTTCCTCATCCTCGC	79589
rs760367343	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717792	AATGTAAAGATTAAG[C/T]GGGATTCGTCTAGCA	79589
rs760373179	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772306	TGCTAACCTGATCAC[A/G]TCTGTGTAAAACCTT	79589
rs760406041	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106786669	AAGAAGGAAAAGATA[A/T]GGTACAGACTGGGAG	79589
rs760417993	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106732599	AGTATACAAAATAAT[G/T]AAGGTAAAGTCCCTG	79589
rs760449536	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784581	ATAGATAAGTAAACA[A/G]GCTCAAAGAATTAAA	79589
rs760458515	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106744564	TCCCAGGTTCAAGTG[A/T]TTCTCCTGTCTCAGC	79589
rs760464719	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106756085	CTCAAAGAAATAAAA[C/G]AGGATACAAACAAAT	79589
rs760485958	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106768347	atccatctggtcctg[C/G]actttttttggttgg	79589
rs760493094	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702468	CACACAGAACAATGC[C/T]TGAGCCTATATAAAG	79589
rs760502509	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784041	TCACCATTTCAACAC[A/G]GCATCTACCAAGTGT	79589
rs760504541	in-del	-/CA			intron-variant	RNF128	GRCh38.p7	X:106707610	ACTTTACTTTTGTGT[-/CA]CTTGGAGAAGGATTT	79589
rs760547497	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106727683	TTCCCTTTTCCTGGT[G/T]TTTCACAAGGGTGTC	79589
rs760601145	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739454	ATGAGCAACCATGCC[C/T]GGCCCTCATATTTTA	79589
rs760630082	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106715857	CAGAATTACCTGCAG[G/T]CTAAACTACTCTTCT	79589
rs760654744	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106703546	TCAGTACACAATACT[A/G]CCTCTCCAGTGAGCA	79589
rs760662700	snp	C/T	2.59514e-05	0.00360209	intron-variant, missense	RNF128	GRCh38.p7	X:106727197	CCGGGGCGCTTAACG[C/T]CTGTAACCCGCACAC	79589
rs760691671	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704796	CCATTTGGGAAACTA[C/G]CTAAGGATGGAATGA	79589
rs760691770	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106704365	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	79589
rs760722905	in-del	-/TA			intron-variant	RNF128	GRCh38.p7	X:106721393	TTAAAAGCTGAACAC[-/TA]TCATCCATCTCAACA	79589
rs760746914	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713085	GGGATTTCACCATGT[C/T]GGCCAGGCTGGTCTC	79589
rs760758298	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106767927	TTTTTAGCATGAAGC[A/G]CTGTTGAATTTTGTC	79589
rs760789933	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752394	GGGAAGAGAACAACA[C/T]ATTCTGCCTGGTAAT	79589
rs760803126	snp	A/G	2.63366e-05	0.00362872	intron-variant	RNF128	GRCh38.p7	X:106694456	TGTCCGTTTATCTTA[A/G]AATGGTATTTCCATC	79589
rs760822380	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106775526	AGCATTAAAACTTCT[C/T]ATCTATTTGGAGAAG	79589
rs760851937	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705917	CAGAACTCAGAGAGA[A/G]GTGGGTAAATCACAT	79589
rs760881947	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106705798	TGTAGTACCATTTCA[A/C]CCATACACACAGGCA	79589
rs760887851	snp	A/C	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106786536	AAAAATATTTTCATG[A/C]CTTGGGTGACAAATA	79589
rs760898424	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759293	AATAATGAATGCTGG[C/T]GAGGATGTAGAGGAA	79589
rs760918312	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106731972	ATATGCTATTACTTA[C/T]AAATTTTGGACTACA	79589
rs760946334	snp	A/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692526	ATATTTGTATTATAC[A/T]TCTGCTGGGATTTAT	79589
rs761021494	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106763046	ACATGTTAGGCTAAG[A/G]AGTCAGATTGTAATG	79589
rs761022025	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741471	CCATTAATGCAGCTC[A/T]GGAAGTATGGTAATT	79589
rs761025528	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770288	TGAATTTGAATGTTG[G/T]CCTGCCTTGCTAGAT	79589
rs761038572	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699476	TCTATCTACTACCAC[C/T]AGTCTAGTACAGGCT	79589
rs761043369	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730956	AGGTTGTGCTCTGCC[A/T]ATTAGTATTTTTTAA	79589
rs761046546	snp	A/G	0.000529661	0.016265	downstream-variant-500B	RNF128	GRCh38.p7	X:106797469	AATTTTTCTCATATA[A/G]TATGTCTGGATTTGG	79589
rs761069651	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106724322	CCTGTAGCACTGCCA[A/G]CCATCTTCTGTATGG	79589
rs761083830	snp	A/G	2.28107e-05	0.00337711	missense	RNF128	GRCh38.p7	X:106773083	TCCTTTTTTATTATT[A/G]CGGCGGCAACTGTGG	79589
rs761110166	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709377	ATGTTAGCAAACTGA[C/T]AAATATTGATAAAAC	79589
rs761123257	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106763800	AGGCGTGGGCCACCA[C/T]GCCCGGCCAATTCAG	79589
rs761147825	in-del	-/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698637	TGCATCTCCAAGACA[-/C]CACTCACTCTATCTT	79589
rs761232403	snp	A/G	0.000115405	0.00759536	missense	RNF128	GRCh38.p7	X:106795697	AAGAGACTGCTGTTC[A/G]AGAAATTAAATCTTA	79589
rs761254459	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106786145	AAGAACAACTTTGGA[A/T]GATTCATGCTACCTG	79589
rs761264737	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106764280	TTGTTTTGTTTTTCA[A/T]CCTTCATCTGACCAC	79589
rs761297271	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785704	TTAAGCCACTGAATT[A/G]TGATAATTTGTTACA	79589
rs761300150	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106719643	ATGGCAAGATCATAG[A/G]TATTTATTTTAGATA	79589
rs761317708	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106739594	TATGGTAGCTTTTAT[A/G]TCAGGTTTATGTGGC	79589
rs761327244	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764002	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	79589
rs761331425	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106697742	TTTTTCTGAAGGGGA[A/T]AATTTCAGTTTGAGA	79589
rs761358178	snp	C/T	4.57593e-05	0.00478305	missense	RNF128	GRCh38.p7	X:106791166	ATCGCAGCGAGACCG[C/T]ATCATCTGGATATGC	79589
rs761378133	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770390	GGTACACCAATCAGA[C/T]GTAGATTTGGTCTTT	79589
rs761383999	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106714541	AGTTGATACAATCCA[C/T]CCACCTTACTCGAAT	79589
rs761384347	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106735925	AACACACACACACAT[-/A]AAAAAATGCACATTC	79589
rs761397508	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106781654	CACTTGTCTTGCATC[C/T]ATATTTAAAGAAAAT	79589
rs761425796	snp	C/G	2.43629e-05	0.00349011	intron-variant	RNF128	GRCh38.p7	X:106773201	ATTAAAAAAAATTTA[C/G]TGTTCTAATTGTAGT	79589
rs761439629	snp	A/C	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106746857	GCATGAAACTCTAGC[A/C]ATGTCTCGTTATTAT	79589
rs761448970	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106780464	CTTCTGTTAAGAAAA[C/T]TGGCCAACAACCAGC	79589
rs761452445	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106710683	AATTGCTTGAACCCA[A/G]GAGGCAGAGGTTGCA	79589
rs761481824	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106771459	TCAGCAATGGCGTAC[A/G]CCCCTCCCCCAGCCC	79589
rs761494579	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106774619	CCTATTATTTCTACC[C/T]TCATTATATATCCAG	79589
rs761504209	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106709522	GTGTTGTTTTATATT[G/T]ACTTGGAACATTTTT	79589
rs761519470	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713951	GAGGCTGAGGCAGGC[A/G]GATCAAGAGGTCAGG	79589
rs761564525	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785412	AGATTATCCTGGATT[A/C]TCCAGATAGATTCAA	79589
rs761568189	snp	A/G	0.000124769	0.00789739	intron-variant, missense	RNF128	GRCh38.p7	X:106727028	CCCGGTTCCCGGGGG[A/G]CTGAAGCAGTGTGGA	79589
rs761591875	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106704226	AGATCACGAGGTCAG[C/G]AGATCAAAACCATCC	79589
rs761596064	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106774103	AATCAGAGTGGGCCC[A/T]TAATGCTACCCAGGA	79589
rs761622262	snp	A/G	0.00791544	0.0624105	intron-variant	RNF128	GRCh38.p7	X:106735740	TTTGGCCTTTTGAAT[A/G]TAGCTATCTAATCCA	79589
rs761630654	in-del	-/TTCCTTCCTTCCTTTT			intron-variant	RNF128	GRCh38.p7	X:106739118	TTCTCTTCTCTTCTC[-/TTCCTTCCTTCCTTTT]TTCCTTCCTTCCTTC	79589
rs761642293	in-del	-/ATT	0.01368	0.0815649	intron-variant	RNF128	GRCh38.p7	X:106704285	TAAAAAATACAAAAA[-/ATT]AGCCAGGCGTGGTGG	79589
rs761642447	snp	C/T	0.00105904	0.0229869	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693743	GAATAAAGTTGATGG[C/T]GTTATTTATTACTAA	79589
rs761679294	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106749660	CCTGTAATCCCAGCT[C/G]TTTAGGAGGCCATGG	79589
rs761683703	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717868	TACTTATTCACTGCT[A/C]CCTATTACAACTTGC	79589
rs761723984	snp	A/C	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106728711	TGAGTTCTTTTAGCC[A/C]CTTCTTTGCCTCTAC	79589
rs761730215	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106703759	ATAGAAGGTGATAGC[A/C]GAGAAGTCAAAGACC	79589
rs761731982	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106793775	ATTTTTGTCAAGAAT[A/G]CTACAGAAGTGATGT	79589
rs761736296	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751400	TAGACCAGCCCTAGC[C/T]GGAGGAGAATTGTCC	79589
rs761753435	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766316	ACAATGGTTGAACTA[C/G]TTTACACTCCCACCA	79589
rs761762390	snp	A/T	2.35112e-05	0.00342856	missense	RNF128	GRCh38.p7	X:106694335	TCAAACAGCGGGCAG[A/T]AGAAATGCTGATGCT	79589
rs761770229	snp	A/G	0.0570788	0.159001	intron-variant	RNF128	GRCh38.p7	X:106757478	TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC	79589
rs761774551	snp	G/T	0.00060423	0.0173709	intron-variant, missense	RNF128	GRCh38.p7	X:106726918	GCGCGCGCGCCATGG[G/T]GCCGCCGCCTGGGGC	79589
rs761785575	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106730747	CATAATTCATGAAAC[A/G]TTTACAACGTTATGC	79589
rs761786008	in-del	-/ACAAAAGG			intron-variant	RNF128	GRCh38.p7	X:106759155	CTCAAAAGAAGACAT[-/ACAAAAGG]ACAAAAGGCAAACAG	79589
rs761787310	snp	A/G			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693733	TTGACATGTAGAATA[A/G]AGTTGATGGTGTTAT	79589
rs761806265	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106784626	TTATTCATTGAGTAA[C/G]TGATAAAGTCAGATT	79589
rs761811887	snp	C/G	2.41368e-05	0.00347388	intron-variant	RNF128	GRCh38.p7	X:106791278	GCCCTGCAATCCATT[C/G]TAGATCATATGCCTG	79589
rs761813737	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106770727	GAAGTTTGTTATTAC[C/T]GATCATCTGAAGCCT	79589
rs761820925	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696514	GCTGTCTTTTCACTC[A/G]TGTTTTGTTTTGTTT	79589
rs761878680	snp	G/T	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106740203	CCAGGGACCTCACAT[G/T]TTTAGCCTCTGTTGT	79589
rs761896553	snp	C/G	6.98007e-05	0.00590724	intron-variant	RNF128	GRCh38.p7	X:106790321	ATGAAGAATATATGC[C/G]TGGGCTTTGGAGAAA	79589
rs761906470	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106719303	CAACTCACTTCAACC[A/T]CCCCCACCCTGGGTT	79589
rs761964005	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106720820	ATAGGATATCATTAC[C/T]TGTTGTGAAAATCAA	79589
rs761968673	snp	A/G	2.28381e-05	0.00337913	missense	RNF128	GRCh38.p7	X:106694220	GCATCCCTAAGAACA[A/G]TAACTACCAAGCTTG	79589
rs761974410	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106795362	TAAGCACATGTACGT[G/T]AATCAAAAAAGCAAT	79589
rs762035020	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106776720	CAAATTTATGGAATT[A/T]TTTTTTGTAAAATTG	79589
rs762054047	in-del	-/ATA	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794205	CGTTTCTTTCATTCT[-/ATA]ATATCATTCTCATCG	79589
rs762062578	snp	C/G	2.3091e-05	0.00339779	intron-variant	RNF128	GRCh38.p7	X:106790176	TAATTATGTTTTTTT[C/G]CTGAATTAGCCATAT	79589
rs762079603	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707614	TTACTTTTGTGTCTT[A/G]GAGAAGGATTTGGGG	79589
rs762090247	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106761622	GAATGAGATCATGTA[C/T]GATCTCATGAGTACT	79589
rs762113077	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106760755	TAAGTATCCATCAAT[G/T]GATGAATGGATATAG	79589
rs762123904	snp	A/T	2.27975e-05	0.00337612	missense	RNF128	GRCh38.p7	X:106773050	GTGAATCACTATTCA[A/T]TTTTTTTCGTTTCTG	79589
rs762133845	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726272	GCCCTTCCCCCCTCT[A/G]GAGAATCAGTAAATA	79589
rs762170423	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786656	AGGCACTGTTAAAAG[-/A]AAGGAAAAGATAAGG	79589
rs762171747	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106702239	AGCCCTTTCAAGTAC[-/A]ATTTCATCTCCCTTT	79589
rs762207107	snp	C/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106764583	GAAGCAGGAGAATCA[C/G]TTGAACCCAGGAGGC	79589
rs762208573	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106779964	CTTACTATAATTCTT[C/G]ATTTTAAATATCTTG	79589
rs762216178	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106715610	GCCTTTCTGATACCT[A/T]GACTGTAGACAGAAT	79589
rs762245949	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106759134	CAAAAGATCTGAATA[A/G]ACATTTCTCAAAAGA	79589
rs762248869	snp	C/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106787447	GGGATGAGAGGAAAG[C/G]TTAACTACAAAGAGT	79589
rs762260070	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106700765	ACGTACAGAAAACAC[A/G]TAGTCAATTTGTGTT	79589
rs762281789	in-del	-/AT			intron-variant	RNF128	GRCh38.p7	X:106780770	TACAATAGTGGAGAG[-/AT]CATGGGCTTTAAAGC	79589
rs762289795	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106761595	ATGGAATATTATACA[G/T]CCATAAAAAAAGAAT	79589
rs762296495	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106782352	GATGTCCAACTGACT[C/T]ATGATCTATGTGGAA	79589
rs762367174	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106752548	ACTTAGATCACAACA[C/T]TCAATTCCCTTTGAA	79589
rs762381291	in-del	-/G	2.44272e-05	0.00349471	intron-variant	RNF128	GRCh38.p7	X:106785049	TTTCTAATACCTGCT[-/G]TTTTTTTTTTTACAG	79589
rs762394057	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106784195	TGCAGCATCACCAGT[A/C]ACTTCAAATTGACAA	79589
rs762444313	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106735811	CTTCATGTGCCTTGA[C/T]GACTAAAAGAATTTT	79589
rs762451778	snp	A/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725385	AAGAGTATCAAGTAC[A/T]GAATTGGTCCATGCT	79589
rs762460582	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106782824	GGGCTGACACTAGCT[C/T]TGATATTTCAAGCAA	79589
rs762503728	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106736610	CTCCCATAAATTCTA[C/T]AAAAACCACCCATTA	79589
rs762503938	snp	A/G	6.83862e-05	0.00584709	synonymous-codon	RNF128	GRCh38.p7	X:106773022	AGAAGTAGGGAAAAA[A/G]CATGGCCCTTGGGTG	79589
rs762514948	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106764660	TAAGGAGCGAAACTC[C/T]GTCTCAAAAAAAACA	79589
rs762522478	snp	A/G			synonymous-codon	RNF128	GRCh38.p7	X:106694356	TGCTGATGCTGTTGT[A/G]ATTTACAATGCTCCA	79589
rs762529987	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106710806	GGAGAAATTCACAAA[A/G]AAAATAGCCAACTAT	79589
rs762550694	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106712385	AAAGAAAAAAGTTAA[C/T]TTTAAGATCTCAAGA	79589
rs762581901	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106737540	TTGTTAATAGCATTG[C/T]TTAGGGAATAATGAC	79589
rs762585764	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791399	CCCCTACCTTAATAT[A/G]CATATATTCAAATGT	79589
rs762587844	in-del	-/CAAAAA			intron-variant	RNF128	GRCh38.p7	X:106760893	CAATTGCAACAAAAG[-/CAAAAA]CAAAAACAAAAACAA	79589
rs762591009	in-del	-/GAAAA	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106691966	CCTACACAAAATAAT[-/GAAAA]GAAATCTTAAGATAA	79589
rs762604790	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106782976	AAAATAGAAGGGAAG[A/T]TATTTGTGCTGAAAT	79589
rs762615935	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765603	ATATTTGGATAATAC[A/C]CTCATATTGGAAGAA	79589
rs762659396	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106747386	CAAATTAAGGACTTT[C/T]TTCTTTTCTTTGGGA	79589
rs762720173	in-del	-/TGT			intron-variant	RNF128	GRCh38.p7	X:106740213	CACATTTTTAGCCTC[-/TGT]TGTTGTTGTTGTTGT	79589
rs762728051	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766852	TTATGGTTTTAGGTC[G/T]AATATTTAGGTCTTT	79589
rs762735979	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106719146	AGGAGCCCCAGCCTT[A/G]TTAGAAATTATCCAG	79589
rs762764321	snp	A/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106724751	GGTGCTTCTCTGTTA[A/T]CCACTACTACCCTGT	79589
rs762783279	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766368	TCTCCACATCCTCTC[C/T]AGTACCTGTTGTTTC	79589
rs762831067	snp	C/T	5.21492e-05	0.00510606	intron-variant	RNF128	GRCh38.p7	X:106694445	AAGAGAGTTAATGTC[C/T]GTTTATCTTAGAATG	79589
rs762853997	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726646	CCAGCCACCTCTACC[C/T]CCAGTCGGCTGGGCG	79589
rs762937180	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720064	TTACTGGAAACCTGA[A/G]AAGGAAAGATAGGAG	79589
rs762945759	snp	A/G	4.79634e-05	0.00489687	intron-variant	RNF128	GRCh38.p7	X:106791044	ACTGAGAGGCTTTTA[A/G]TTTGTTACATGTTCT	79589
rs762964411	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106697278	AGAGAAATATTTGGT[A/G]GTTTTTGTGGCGAGG	79589
rs762966167	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106792927	TTTGTCTGGGATTAC[A/G]TATTACTAGTTTAAG	79589
rs762999468	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106794278	AACTTGTTCAAGTTG[G/T]TTTTTGTGTTCTTTC	79589
rs763021355	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106795468	GGAATGAATATGGTA[A/C]TCAGTGTATGTTGAA	79589
rs763023453	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698355	TTAGAGTCAAGTGTG[C/T]GGCATTCAGAATCTC	79589
rs763027759	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106731740	ACTCCTAGCACTCCT[C/T]CTCCAGTAAATAGAT	79589
rs763053302	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106735721	ATGAGAATTTAAGAA[C/T]TGCTTTGGCCTTTTG	79589
rs763080663	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769662	AATACAGCACACTGA[C/T]GGGTCTTGATTCTTT	79589
rs763085267	snp	A/G	0.000125761	0.00792872	missense	RNF128	GRCh38.p7	X:106694012	TGAGCAATGAACCAG[A/G]AGAATAGGTCCAGTT	79589
rs763095274	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761744	TCCCTGTCCTCTGCT[C/T]ATCTATGTATTACTT	79589
rs763104837	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106737610	TTTTCCCAAACATTT[C/T]TGATCCTTGGTTAGT	79589
rs763167914	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106738985	CTGTTTGACTTTGTT[A/C]AATGCATTATTTTCT	79589
rs763199995	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106722677	GGGTTTCTGGGGACT[A/G]ACTCACACTTAACCA	79589
rs763225428	in-del	-/AAA	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106713201	CCGATGAAGTTAATT[-/AAA]AAAAAAAAATACAAG	79589
rs763227072	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750329	CAGCTTTAGGTTTCA[C/T]TGAAGATAACTAGTG	79589
rs763247543	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106790065	TTTTATGAATAGTGT[A/G]TTTAAAAGGAAAGGC	79589
rs763280607	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722347	TCAAACATATATACA[C/T]GCAGATCCCCTGGGG	79589
rs763296124	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106788886	AATGTATAATATATT[A/C]TATATTATACATTAT	79589
rs763302148	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106793120	ACGGAAAGGTCACCA[C/T]CAGAGTTTCTGACTC	79589
rs763323144	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106769004	GGAGCAGGTTGTTCA[A/G]TTTCCATGTGGTTGT	79589
rs763325537	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749475	CACACACACTAAAAG[C/G]GTTTCTTTCTTGTTC	79589
rs763349308	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106744452	GGTTAATTACTTTAA[C/T]ATGAACTTATGATTA	79589
rs763354783	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787606	ATACCTTAATTTTTT[A/T]AAAATGAGAAAAGTT	79589
rs763358986	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692707	CACCTCCATCAACAA[A/C]GTCTCCTATTTTTTT	79589
rs763365576	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106776853	GGGAGGGAAATGGCC[C/T]TGCTGTACAAAGTTA	79589
rs763378444	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777655	AAAGAAGGATGGAGG[C/T]CTTCATGATAATCCA	79589
rs763383666	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733117	ACATCATATTAGGTA[-/T]TATAAATAATCTAGA	79589
rs763385558	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106744114	GTTGGGTGGGGGAAG[G/T]GGGGAGGGATAGCAT	79589
rs763389879	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106777781	TCCAGACCAACCTGT[A/G]CAACATGGCAAAACC	79589
rs763409082	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106779719	ACAGTTATGTTCTTC[A/G]TGAGAGTGGTCTGCA	79589
rs763410428	snp	A/G	3.4568e-05	0.00415726	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727105	CCGTACGGTGTGGGA[A/G]CTGAGCGAGGAGGGC	79589
rs763474393	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106712390	AAAAAGTTAATTTTA[A/G]GATCTCAAGAAGAAA	79589
rs763489630	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707412	ATAGGACATATTTTA[A/G]GTTGTCTTCTATTTA	79589
rs763515253	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777923	TGCAGTGAGCCGAGA[C/T]CATGCCACTGCTCTC	79589
rs763524890	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106768216	CTTTGGTATCAGGAT[G/T]ATGCTGGCCTCATAA	79589
rs763550932	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106706857	GACAGTAAAAACTAC[A/G]GTAGTAGCAAGATGA	79589
rs763560731	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717799	AGATTAAGTGGGATT[C/T]GTCTAGCACATTTTT	79589
rs763636645	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106744569	GGTTCAAGTGATTCT[C/T]CTGTCTCAGCCTCCC	79589
rs763676743	in-del	-/AAAT	2.62812e-05	0.0036249	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693990	TTAAATTTTATACTC[-/AAAT]GAATGAGCAATGAAC	79589
rs763766205	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698712	TCCCCTTCCAAGCCC[A/T]ATCTCCAGACTGTAA	79589
rs763768486	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106769899	GTACCAGTTGTTCCT[C/T]TCCATGTTTAGTGCT	79589
rs763799304	snp	C/T	2.50828e-05	0.00354129	intron-variant	RNF128	GRCh38.p7	X:106772878	ATACTAAGAATGTTT[C/T]ACCAAACTAAAACTG	79589
rs763831784	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106737852	CATTTTGGCAAAAGG[G/T]CAGGATATGTAAGAA	79589
rs763836387	snp	C/G	2.28271e-05	0.00337832	missense	RNF128	GRCh38.p7	X:106772958	GCAATCTGAAAGGCA[C/G]AAAAATTCTGCAATC	79589
rs763865973	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106734015	TTATCATTTTATTCT[G/T]TTGCTCTGTATATAG	79589
rs763894815	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693621	CCCCAGAGTCCAGTT[C/T]CTCTTTCCAATCCAC	79589
rs763912306	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765784	AGGTTTGTCACATAT[A/G]TTTACATGTGCCATG	79589
rs763923095	snp	A/G			utr-variant-3-prime	RNF128	GRCh38.p7	X:106796707	TGTTTGAAAAAGAAG[A/G]GGGGGAGAATTCCAG	79589
rs763966902	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717210	TCCGTCTCAAAAAAA[A/G]AAAAAGAAAGAAAGA	79589
rs763968965	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106728562	GAGTCACTGGAAGGA[A/G]GAAGCTGCTTATTTG	79589
rs763973487	in-del	-/AAC			intron-variant	RNF128	GRCh38.p7	X:106764680	CAAAAAAAACAAAAC[-/AAC]AACAACAACAACAAA	79589
rs763990808	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106728280	ACACGTGTAATAGCA[C/G]TGTATCATAGTTTTT	79589
rs763991892	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106749392	AAGGATAGAAAAAAG[A/C]TAAAGGGAAAAAGAG	79589
rs763992994	snp	G/T	2.39538e-05	0.00346068	intron-variant	RNF128	GRCh38.p7	X:106791046	TGAGAGGCTTTTAAT[G/T]TGTTACATGTTCTTT	79589
rs764020902	snp	A/G/T	4.57621e-05	0.00478324	missense	RNF128	GRCh38.p7	X:106791165	AATCGCAGCGAGACC[A/G/T]CATCATCTGGATATG	79589
rs764022203	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106727715	AGCCTTGGATTAAGT[A/G]GTGGTGGGCATCGGG	79589
rs764038304	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767103	TACCAGTACCATGCT[A/G]TTTTGGTTACTGTAG	79589
rs764051025	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106782952	CTCTATTATTATCTT[A/T]CAAGTAACAAAATAG	79589
rs764073863	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754136	CATTTCATCCAACAG[A/C]TACAGAAGACACAAT	79589
rs764095583	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106735765	AATCCATATGATAGT[C/T]GGTGTTACCTTTTAT	79589
rs764097993	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716274	CTCTGACCACTCTTT[C/T]GTTTAAATACCACAC	79589
rs764125236	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106749591	ATTTGGGAATGTGCA[C/T]GGGTTTTCACTAGTT	79589
rs764138144	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693005	AGTTGACCCCGTAGC[A/G]TATGTGTCCTAATGC	79589
rs764144586	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106710495	GGGCACTGTGAATCA[C/T]GCCTGTAATCCCAGC	79589
rs764149438	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704938	TGAAATGTAAGAGCA[C/T]TATTCACAAGGGAGC	79589
rs764149551	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106694655	AGCAATATAAGTTTC[C/T]TCAGTGGGCATTATA	79589
rs764155164	snp	C/T	2.35997e-05	0.00343501	synonymous-codon	RNF128	GRCh38.p7	X:106787941	CCCTGATGGAGATAG[C/T]TGTGCTGTGTGCATT	79589
rs764197956	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106759475	ATATCAAAGAGATGT[C/T]TACACCCCCGTGTTT	79589
rs764244367	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766530	TTGAGAAGTGTCTGT[C/T]CATATCCTTTGCCCA	79589
rs764257658	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696424	AGGAATCAAGTGTGG[A/G]TATGAAAACTAGATG	79589
rs764270893	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740507	TAAATAAACAATTGA[A/G]TAAACAGTGGAATTC	79589
rs764282749	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775570	CTTTTAAAAATTACT[C/T]AATGGACTATATCTG	79589
rs764287121	snp	A/G	2.49492e-05	0.00353185	missense	RNF128	GRCh38.p7	X:106694018	ATGAACCAGGAGAAT[A/G]GGTCCAGTTTTTTTT	79589
rs764302414	snp	C/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106750738	AAGCATGACATCACA[C/G]AAAAAAAAAGAGAGA	79589
rs764351781	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106791627	AGAATTCAATTTATA[A/C]AAGTTTGATTTATAC	79589
rs764356983	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767969	CTGCATCTACTGAGA[A/T]AATCATGTGGTTTTT	79589
rs764378317	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763993	TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG	79589
rs764419162	snp	C/T	0.000139943	0.00836374	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727282	CCTCATCCAACGCGG[C/T]GGGGGCTGCACCTTC	79589
rs764424856	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106777862	GTAGTCCCAGCTACT[A/T]GGGAGGCTGAGGTGG	79589
rs764426772	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106770365	GGTTCCATTCTCCCC[A/G]TCACTTTCAGGTACA	79589
rs764479860	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106753953	AGGTGTATAAAGCAA[A/G]TATTATACAAACTAG	79589
rs764515794	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706254	TTCTGGCTGACAATT[A/G]GATTTTCCAAATTGG	79589
rs764519002	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714336	GTTGAATTCAAATAA[C/T]GCATTATACAATTCT	79589
rs764521358	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704336	TACTCGGGAGGCTGA[C/G]GTAGGAGAATGGCGT	79589
rs764544886	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106727870	TACTAGATTGTGCTA[C/T]TGTGCCCTGTTAACC	79589
rs764583922	in-del	-/TGTT			intron-variant	RNF128	GRCh38.p7	X:106767511	CGTGATTTGGCTTTC[-/TGTT]TGTCTGTTATTGGTG	79589
rs764601655	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735512	AGTATTTGTTCTCTT[C/T]ATTATTATTTTTCTA	79589
rs764618363	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715007	ATGAGTGAAGTTGCT[A/G]TGAAAATTTGTGAAT	79589
rs764647422	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698780	GTTTAAAATCCTTCC[A/G]TGGCTTCCCATGACA	79589
rs764658178	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726559	AGCCACACAGCCTCA[A/G]ATCCTATTCTAACAT	79589
rs764668150	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770029	AGTTTGGCTGGATAT[A/G]AAATTGTGGGTTGAA	79589
rs764672523	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106724387	TTATCCACAGAGAAG[C/G]ATCTCTAAACTTCAG	79589
rs764673641	snp	C/T	0.00021657	0.0104038	intron-variant	RNF128	GRCh38.p7	X:106727437	CCCTCCAGACCTCTG[C/T]CATGGCCAGTTTCTC	79589
rs764685226	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106759028	GAAAATATTTGCAAA[C/G]TATTCATCTGACAAG	79589
rs764685541	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786545	TTCATGACTTGGGTG[A/G]CAAATATTTCTTAGA	79589
rs764693562	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774391	ATTATTTTTGTCTTT[G/T]GTATACTCAAGGACA	79589
rs764694014	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106745788	AAAAAAGTTGCCACT[A/T]AACAGGACTTTGAAG	79589
rs764696954	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709558	TTATAACTTCTTTTT[C/T]TTTTTTAGATGGAGT	79589
rs764698162	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106780472	AAGAAAATTGGCCAA[C/G]AACCAGCTTCTTTGA	79589
rs764740512	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785803	CAGTTGAAAACTACC[A/G]TTCATGGGTAAAACA	79589
rs764826308	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735746	CTTTTGAATATAGCT[A/G]TCTAATCCATATGAT	79589
rs764854497	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106710177	ATTCCTTTAATATGG[C/T]TGTTTTCCTGACCCT	79589
rs764878701	snp	A/G	0.000118097	0.0076834	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727249	TTGGGGAAGCACCGT[A/G]CAAGTCTCTTGGTTG	79589
rs764905900	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106712213	TTCAAAGCCAACTTC[A/G]AGTGTCTTTTTATTA	79589
rs764917784	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699630	ATCACTCCTCTTCTC[A/T]GAACTCCCCAGTGAC	79589
rs764921435	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764025	TGGAGTGCAGTGGCA[C/T]GATATCAGCTCACTG	79589
rs764930185	snp	C/T	2.36097e-05	0.00343574	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795733	TGTGTAAATAGAAAA[C/T]TTGAACCATTAGTAA	79589
rs764933587	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106782661	TCTTCTGGGGGTTGT[C/T]GTGAGGATTAAATGA	79589
rs764957297	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106760104	AATTTTATAAAAAGA[A/G]TAAAAAATTTAGGAA	79589
rs764994796	snp	A/C	1.64749e-05	0.00287005	missense	RNF128	GRCh38.p7	X:106694258	AACACTGAGTTTAGT[A/C]ATACTAAGAAGCCCT	79589
rs765010574	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106762171	ACATTGCTGTTTGCT[A/G]TAGTCACCCTACTGT	79589
rs765014661	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106736524	GATTCCACTTCTTTT[C/G]ATGTAGTAGTAAACA	79589
rs765018123	snp	A/C	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106755271	GCCATGACAAATAGT[A/C]CCCCAGTAAAGAAAA	79589
rs765038572	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106717046	TCTCTACTAAAAATA[C/T]ATAAAAATTAGCCTG	79589
rs765069060	snp	A/G	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106728912	TATCTCTCTTGGCCG[A/G]TAATTCATTGATTAG	79589
rs765078214	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106774127	CCCAGGAATCACACT[A/G]TGTTTTCTTGGCCAT	79589
rs765089695	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106699191	CACATAGCAGCCAGA[A/G]TGATCCTGTGGAAAA	79589
rs765109505	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106747192	TAAATTTTATAGTTT[A/G]TGTTAATGATTTTTG	79589
rs765109699	snp	C/T	0.00528398	0.051128	intron-variant	RNF128	GRCh38.p7	X:106757510	AACACCGCATATTCT[C/T]ACTCATAGGTGGGAA	79589
rs765110730	snp	C/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693755	TGGTGTTATTTATTA[C/G]TAAGGTAGTCCTGGT	79589
rs765113366	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708488	ATACCATGTGAATTT[C/G]AGTAGAGTATTAAAA	79589
rs765119517	snp	A/C	2.28747e-05	0.00338183	missense	RNF128	GRCh38.p7	X:106790231	ATGGCTGTTAGAACA[A/C]AGGACTTGCCCCATG	79589
rs765134685	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106768029	CATTTATTGATTTGC[G/T]TATGTTGAACCAGCC	79589
rs765168261	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717907	ACAAGGGTAAGATTC[C/T]GTTGCAAACTGGACA	79589
rs765180735	snp	C/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725392	TCAAGTACAGAATTG[C/G]TCCATGCTTAATCTT	79589
rs765185877	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106745055	CATCCACAAATTATT[C/T]ATCTGTGACCTTTTG	79589
rs765219997	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733075	TCCCCTAAATGATAC[A/C]GTATAACAACTATTT	79589
rs765239750	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106731331	GTTGTACTTTTCTCA[A/G]ATAACTGCTTCTCCC	79589
rs765241755	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106753612	TAAGAACTTATCAAT[A/G]ATAACATTGAATTTA	79589
rs765251558	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791316	CTCTTGCTTTTTAGC[A/G]TTTGTTCCATTCAGC	79589
rs765263816	in-del	-/GAG	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106780545	TCTCTTAGGATTAGA[-/GAG]GAGGAGGGGAAAGGC	79589
rs765284830	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696538	TTTGTTTTGACACAG[A/G]GGATGGGGGAAATCC	79589
rs765304673	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790697	GATACAACATAAAAT[C/T]GAGCTCAAATCTTGA	79589
rs765345593	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106760812	ATACTATTCAGCATT[A/T]AAAAAGCAGCAAATC	79589
rs765351459	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720295	ATTTGATCTCCCAGT[A/G]GCAATCAAGTGCATA	79589
rs765388603	snp	G/T	2.3153e-05	0.00340234	missense	RNF128	GRCh38.p7	X:106785083	CAATTAAAGGCAGAT[G/T]CTAAAAAAGCTATTG	79589
rs765402114	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106748533	ATGGAATCAGTCATC[A/G]AAAGATGAATGGATA	79589
rs765404711	in-del	-/ATAGG	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732270	AAAACAAAGTATAGT[-/ATAGG]AATCTCTTTTTGTTC	79589
rs765412930	in-del	-/GT			intron-variant	RNF128	GRCh38.p7	X:106779349	TCCCTACACAGTTAC[-/GT]GTGTGTGTGTGTGTG	79589
rs765423132	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716164	TCAAGGTCCTGCAGT[C/T]ATCCATGAAACAGCC	79589
rs765438139	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106733825	CATGCCTCAGCCTCT[C/T]GAGTAGCTGGGATTA	79589
rs765455947	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106741952	TTATAAAAGGAGGTT[C/G]AATTTTATTCCGTAG	79589
rs765470307	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775825	TTTGGCTTCATTAGA[A/T]TGTTAGGCAAATTTA	79589
rs765501604	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106786929	TCATTAGAATGGCTA[A/G]AATGCATACAACTGA	79589
rs765511610	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106712212	TTTCAAAGCCAACTT[C/T]GAGTGTCTTTTTATT	79589
rs765528621	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752552	AGATCACAACACTCA[A/G]TTCCCTTTGAATGCT	79589
rs765531773	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106691857	CAAAGCATTGTCTAC[A/G]AAGATTATAAGATAA	79589
rs765533524	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786741	AGAATATAAAGAACT[C/T]TTAAAACTTAACAGT	79589
rs765559218	snp	A/T	6.84752e-05	0.00585089	missense	RNF128	GRCh38.p7	X:106795634	TGGCAGTGGATGTTA[A/T]TCCTCATGTTGACAA	79589
rs765565100	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106711095	TTTTGCTAAAAAAAA[A/T]CACTGAATCTAATTC	79589
rs765579205	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761652	TCAGATACAGCCACA[C/T]AGGACTATTGTCATT	79589
rs765591304	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106789904	TAAGATTTGAAATAA[G/T]GAACAAAGTCTTAGG	79589
rs765594791	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787527	ATAAGGATTAAGTGA[C/T]GACATATTTTTCAAA	79589
rs765627485	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106721285	TGTATCCAGCATCAC[C/T]TAGATGCCAGGATAC	79589
rs765638326	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106775629	TATATGGCTGATAAT[C/T]CTTTTTGCTTATAAA	79589
rs765749648	in-del	-/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106724655	TTGTGTTGTTTTCTG[-/C]CTAGAAAAGTTTACT	79589
rs765763718	snp	C/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106741641	TATATAGAGAGAGGA[C/T]GCACACCTTAGACTG	79589
rs765803552	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106777673	TCATGATAATCCACG[G/T]CCTCTTAATTAAGAT	79589
rs765809225	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106767169	CCTCCAGCTTTGTTC[C/T]TTTGACTTAGGATTG	79589
rs765814863	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106744695	CTATCTCCTGACCTC[A/G]TGATCCACCCACCTC	79589
rs765821524	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106704621	GAAGCACAGGGAACC[C/T]ACAGTGAAGAGAAGA	79589
rs765829542	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106722576	AAGTCTCCATAGAGT[A/G]GAAGTACTTTGTTGC	79589
rs765850913	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106736654	CCTGATTAAATACAC[A/G]TTTCCTTCATGTACC	79589
rs765888495	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706099	ACATGATACCTCCAC[A/G]ACATGGGAGACCAAG	79589
rs765901824	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106737592	GTTCAGTACAGGCAC[C/T]TTTTTTCCCAAACAT	79589
rs765908726	snp	C/T	2.43005e-05	0.00348563	intron-variant	RNF128	GRCh38.p7	X:106787904	TCAGAGTAACAATAA[C/T]TACTTGCTTGTAGGA	79589
rs765968288	snp	C/T	7.10038e-05	0.00595792	intron-variant, missense	RNF128	GRCh38.p7	X:106727091	CACACGGGAGTGAAC[C/T]GTACGGTGTGGGAGC	79589
rs765996955	snp	C/T	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106771559	CCTCTGAGCCAGGCG[C/T]GGGTTATAATCTCCT	79589
rs765999230	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106787624	AATGAGAAAAGTTAT[A/G]GAGCTTGCACAAATG	79589
rs766009727	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725235	CCATGCTATTGGTCT[C/T]ATATACCCACTTTGA	79589
rs766017076	snp	A/G	2.2836e-05	0.00337898	missense	RNF128	GRCh38.p7	X:106795627	AATTCTGTGGCAGTG[A/G]ATGTTATTCCTCATG	79589
rs766033255	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752871	GAGATTGAAATACTT[C/T]AAAAAAATCAAGCAT	79589
rs766058359	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786904	GCCACAATGAAATAC[A/C]ACTACGCATTCATTA	79589
rs766083332	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715746	TCCTTGGTATGCTTT[A/G]GATATATTTAGATGT	79589
rs766095240	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759094	ACTAAATAGGAAAAT[A/G]TCTAATAATCCGATT	79589
rs766104912	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707752	ACAGCATTCTTTCAG[A/G]TTTTAAAAGCTGTAG	79589
rs766110046	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778102	CTGTTTATGTTATCA[A/G]TAAGGCTTCCAGTCA	79589
rs766131422	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106732882	AAATGCTTCCATTGA[A/C]CATGTTGGTGAATGT	79589
rs766134904	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106715217	ATTTGGTGTAGACAC[A/G]TTATTTTTTTTAATT	79589
rs766138256	snp	C/T	4.96555e-05	0.0049825	missense	RNF128	GRCh38.p7	X:106787984	CCAAATGATTTGGTA[C/T]GCATCTTAACGTGCA	79589
rs766153926	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106781913	CCTTAATGCAAGTTC[C/T]ACTGTTCTCCTGGGC	79589
rs766186431	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710822	AAAATAGCCAACTAT[A/G]TTCTGGCCAATTTAA	79589
rs766193471	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106719201	CCATTGCCTGTAGAT[A/T]AAAAAAAAAAATTAC	79589
rs766218301	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106757886	ATACCTGGAACAGGA[C/G]AGATATATCCACTTT	79589
rs766239302	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720083	GAAAGATAGGAGACT[A/G]CATGAGACAAGATGT	79589
rs766255584	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106767853	ATTGGCTGTGGGTTT[C/G]TCATAGATAGCTCTT	79589
rs766285192	in-del	-/TA	2.32264e-05	0.00340773	intron-variant	RNF128	GRCh38.p7	X:106790165	TTTACAACTGATAAT[-/TA]TGTTTTTTTCCTGAA	79589
rs766300694	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106736978	GCCCCATCGAGTATG[A/G]ATTATTATATTATTC	79589
rs766380398	snp	A/G	0.00142426	0.0266478	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795744	AAAACTTGAACCATT[A/G]GTAATAACAGAACTG	79589
rs766426636	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106750061	AGAATAAGCAGTTCA[A/G]TCTGTAACTGAGTGA	79589
rs766438952	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106704537	GGCACGAACAGATGA[G/T]CTGCCTTACTGAAAA	79589
rs766443158	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722469	CTGATCAACAGACCT[C/G]ACTCTTGGTAGCAAG	79589
rs766462496	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106697907	ATTGGTGAGTATATC[C/T]CTATCTATCTACACA	79589
rs766476933	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106751610	CCCCAACTCCAGGCA[C/G]TACAGCTCACAGCTC	79589
rs766479448	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106712253	TTGTATCATCTGCAT[C/G]ACTGCTTCCCATCTA	79589
rs766487646	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784124	TCATATGTATATTAT[A/G]TTCACTTGAGGCATT	79589
rs766496219	snp	C/G	7.4297e-05	0.0060945	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727213	CTGTAACCCGCACAC[C/G]AATTTCACGGTGCCC	79589
rs766498753	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749613	TCACTAGTTTTTAAA[C/G]ATAAGTATGAGGCCA	79589
rs766499265	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106775033	AGTGATGGTTATCTC[A/T]GTGTTTAAAGTTAAT	79589
rs766500058	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106757919	CCACTGTTATGCAAC[A/G]TAGTACTGGAGGTCC	79589
rs766525910	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713244	CCGGGTGCGGTGGCT[C/T]ACACCTGTAATCCCA	79589
rs766538262	snp	A/G			synonymous-codon	RNF128	GRCh38.p7	X:106785067	TTTTTTTTTACAGAG[A/G]CAATTAAAGGCAGAT	79589
rs766595719	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106743093	TCAAACAACTCTTTA[A/G]CTTGAAGATCCACTG	79589
rs766623055	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106761931	ACTTTTTTATTTTGG[G/T]CAGACACTGTCTTTT	79589
rs766685099	snp	A/G			missense	RNF128	GRCh38.p7	X:106694148	CTGCAATAGAGACAT[A/G]TGAATGTGGCGTTTA	79589
rs766820481	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706213	TTTGCAGTGTGGCTA[G/T]GAGGAAATCTCTTAG	79589
rs766835099	snp	A/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106741836	CTAGTCCCTAACATG[A/T]AGTTCATAGTTTATG	79589
rs766842118	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106702578	CTCTCTTCCTTCATT[C/T]GAAGAGTACATTCCC	79589
rs766843999	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696682	ACTCTTCTCTGGCTC[C/T]CCCTACCTCTTCATT	79589
rs766868094	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106697337	ACCTGATTATGGAGT[G/T]GTCTTTTTTGTTTGT	79589
rs766887111	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106696659	CCCTCAGGCCCTTGT[A/G]CTCTTCTACTCTTCT	79589
rs766902958	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794284	TTCAAGTTGGTTTTT[A/G]TGTTCTTTCAACTTT	79589
rs766907592	snp	A/G	2.28815e-05	0.00338234	missense	RNF128	GRCh38.p7	X:106773123	TCTTTTATTCTGCTC[A/G]AAGGCTACGGAATGC	79589
rs766968168	snp	C/T	6.84361e-05	0.00584922	missense	RNF128	GRCh38.p7	X:106773084	CCTTTTTTATTATTA[C/T]GGCGGCAACTGTGGG	79589
rs766982832	snp	C/T	0.00105904	0.0229869	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726136	AGAAGAGGCATCTGA[C/T]GCGGTACATGAAACC	79589
rs767045898	snp	A/C	2.35866e-05	0.00343405	intron-variant	RNF128	GRCh38.p7	X:106727410	CGGGTGAGTGCAGCT[A/C]CTAGATTGCACCCCT	79589
rs767051390	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706869	TACGGTAGTAGCAAG[A/G]TGATGCTCATGAAGT	79589
rs767061032	in-del	-/AATT	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106738816	TTATTGTGAGGTGTA[-/AATT]AAATAATATATGTAC	79589
rs767065886	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106753911	AGATAGAACAAGTGT[A/G]TATATGCACCCAAAG	79589
rs767114551	snp	C/T	2.29295e-05	0.00338588	missense	RNF128	GRCh38.p7	X:106791181	CATCATCTGGATATG[C/T]TTCAGTACAGGGAAC	79589
rs767181313	in-del	-/TT	4.14293e-05	0.00455115	intron-variant	RNF128	GRCh38.p7	X:106785050	TTCTAATACCTGCTG[-/TT]TTTTTTTTTACAGAG	79589
rs767194989	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106742095	CTTGGAGACCAGCTA[A/G]GGGGTTGTTAATGGT	79589
rs767203200	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106775977	GCCTCATATGTTGTA[A/G]TGTGATGTGTAAGAA	79589
rs767211581	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106717059	TATATAAAAATTAGC[C/T]TGGCGTGGTGGCGGG	79589
rs767225574	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106743230	AATGATAAGATTTAA[A/G]TTTTTAAGCAAAAAT	79589
rs767237388	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106707037	GCACCTATTCAAAAT[G/T]TACATACATAGTTCG	79589
rs767242257	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789134	ACTATATACTATATA[C/G]TATATAGTGTATATA	79589
rs767246876	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106736757	TTATTACAAATATGG[G/T]TTAAATAATAATTTA	79589
rs767246926	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106748085	TCTTATTAGTGCTAC[A/G]TTTTAATCAACTGAG	79589
rs767326205	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772166	TTCCACAAAACTTAT[A/G]TAATTGGTGGTAGAG	79589
rs767346387	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783052	ATGGGAGTGAAAGTG[C/T]CTTGATTATCACCTC	79589
rs767355773	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106728384	ACTTATTTCAAGTCT[C/T]AGAGTCTGGGTTCTC	79589
rs767388526	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710868	CTCTCTAGGTTTAGT[C/G]TAGCTTCATGATTTG	79589
rs767401263	in-del	-/T	0.000152528	0.0087316	frameshift-variant	RNF128	GRCh38.p7	X:106694025	GGAGAATAGGTCCAG[-/T]TTTTTTTTGGCTCCT	79589
rs767415948	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760632	TAATCTGGCAATTCA[A/G]TTACTGGGTATCTAT	79589
rs767418194	snp	C/T	1.86604e-05	0.00305448	intron-variant, missense	RNF128	GRCh38.p7	X:106726920	GCGCGCGCCATGGGG[C/T]CGCCGCCTGGGGCCG	79589
rs767445268	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106786445	TCTTCATACCCTATG[C/T]AAACATTATTTCAAT	79589
rs767475995	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106764286	TGTTTTTCAACCTTC[A/G]TCTGACCACAATGGC	79589
rs767479007	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106712612	TTTCTGCCTACACAT[C/T]TAAAATGTTACTCAA	79589
rs767501215	snp	A/C	8.05088e-05	0.00634413	intron-variant, missense	RNF128	GRCh38.p7	X:106727035	CCCGGGGGGCTGAAG[A/C]AGTGTGGACCGCGTA	79589
rs767530048	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106694863	GTGTGTAAAATGTTA[C/T]AGAAATGAGAACTTG	79589
rs767550303	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106730821	AGGGCTGTAAAAAAA[A/C]AAAGTGAATGAACCA	79589
rs767553769	in-del	-/A	0.19611	0.244123	intron-variant	RNF128	GRCh38.p7	X:106714178	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	79589
rs767571463	snp	G/T	2.28363e-05	0.003379	missense	RNF128	GRCh38.p7	X:106694235	ATAACTACCAAGCTT[G/T]TGACCACAACACTGA	79589
rs767594320	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106694489	GAACTGGTCTAGGAT[A/C]TGGCAACAAGGTTGT	79589
rs767595650	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106719355	CCTCTCGAGTACCTG[A/G]GATTACAGGTGTGCT	79589
rs767598522	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106702164	GTTTATAAGGAAATC[A/G]AGATATAGTACCTCT	79589
rs767602314	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766401	GACTTTTTAATGATC[A/G]CCATTCTAAGTCGTG	79589
rs767603355	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106714581	TTTACATGCAATTAT[A/G]TGCATGTTCTGCACA	79589
rs767617789	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106712080	CTAGCCCACCGGTGG[C/T]GGTTAAATCTCAGGC	79589
rs767627809	snp	A/G	4.59374e-05	0.00479235	synonymous-codon	RNF128	GRCh38.p7	X:106795599	AAGTCTACAGCTGGT[A/G]AACCATGAAGCAAAT	79589
rs767650194	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739804	GGTACTAGAATGTTC[-/T]TTTTTTATAGATTTT	79589
rs767659380	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106749687	ATGGTGGGAGGATAG[C/G]TTGAAGCCAGAAGTT	79589
rs767661159	snp	C/T	2.36532e-05	0.0034389	missense	RNF128	GRCh38.p7	X:106694343	CGGGCAGAAGAAATG[C/T]TGATGCTGTTGTGAT	79589
rs767682122	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704296	AAAAAAGCCAGGCGT[A/G]GTGGCTGGCGCCTGT	79589
rs767695914	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106770858	AATTTTCAGCTTTTC[C/T]GCTCTGGTTTCTCCC	79589
rs767705699	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785568	CAGACAGCCTCTAGA[A/G]GCTGGGAAAGATAAG	79589
rs767732838	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106709623	CCAATCTGGGCTCAC[C/T]GCAACCTCTGCCTCC	79589
rs767733068	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762113	TTTGTTTGTGGTAAC[A/T]TCATTCAAAATCTTT	79589
rs767747634	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708080	CAGTCAAATATTTCC[C/T]ACTTCATAATCTTAT	79589
rs767786663	snp	A/G	0.000320476	0.0126545	synonymous-codon	RNF128	GRCh38.p7	X:106790204	TATTTTCCATAAGAC[A/G]TGTGTTGACCCATGG	79589
rs767816803	in-del	-/AT	0.0157677	0.0873799	intron-variant	RNF128	GRCh38.p7	X:106744477	GATTATTTTAAATGA[-/AT]ATATATATATATATT	79589
rs767829071	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106769800	TGTCATTATGATGTT[A/G]GCTGGTTATTTTGCT	79589
rs767877278	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106769156	GTCCATTTTGGAATA[C/T]GTGTTATGTGGTGCT	79589
rs767881080	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106779663	TCAAATTCACCCTTT[C/T]TTCACTGTTCTTCCT	79589
rs767887846	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740364	GGTACAGAGTACAGG[C/T]ACCTTTCATGCATTG	79589
rs767909290	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106736018	CCCTTCAGTATCCAT[C/T]CTACTCAATACTGTT	79589
rs767937203	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106759210	ATTGATCATCAGAAA[C/T]GCAAATAAAAACTAC	79589
rs767960495	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106717576	CCCAGCAAATTTGTA[A/G]GACTTTGTAGACAGC	79589
rs767997227	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766700	GTTTCTTTTGCTGTG[A/C]AGAAGCTCTTTAGTT	79589
rs768000642	snp	A/G	2.42207e-05	0.00347991	intron-variant	RNF128	GRCh38.p7	X:106772899	ACTAAAACTGAATTT[A/G]TTTTATTTTACAGGT	79589
rs768018295	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106722552	GTAAAACCAGTGGGT[G/T]ACCCAGGCAAGTCTC	79589
rs768043546	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762913	TACCTATTGGGCACT[A/G]TGCTTATTACATGGA	79589
rs768084162	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106766811	ATGGCCTGAATGGTA[-/T]TTGCCTAGGTTTTCT	79589
rs768098860	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106793794	CAGAAGTGATGTTGT[A/G]CCCCTTTCAGTGCCC	79589
rs768137438	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106761844	TTTGGTCCCCTGTCA[C/G]TTGGTTTCTAACCTC	79589
rs768156257	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106756400	AGAGATATAGATCAA[C/T]GGAACAGAACAGAGC	79589
rs768156855	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709415	ATTCAAGCAATAATA[C/T]GTTATGAATCTTCTA	79589
rs768175963	snp	G/T	0.000529661	0.016265	utr-variant-3-prime	RNF128	GRCh38.p7	X:106796110	AGCTTGGGCTACATG[G/T]GTCAGGGTTTTTCTC	79589
rs768176561	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106730150	TGCTTTAAAATTTTT[A/G]TTTAGGAGAAAGAAA	79589
rs768182083	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698526	GATGACAAAAAACTT[C/T]GGTAAAACTAACTCA	79589
rs768185608	snp	A/T	2.40929e-05	0.00347072	intron-variant	RNF128	GRCh38.p7	X:106773195	TCCACTATTAAAAAA[A/T]ATTTACTGTTCTAAT	79589
rs768220666	in-del	-/T	0.00464035	0.0479441	intron-variant	RNF128	GRCh38.p7	X:106785050	TTCTAATACCTGCTG[-/T]TTTTTTTTTTACAGA	79589
rs768221747	snp	A/G	2.41485e-05	0.00347472	synonymous-codon	RNF128	GRCh38.p7	X:106694371	GATTTACAATGCTCC[A/G]GAGACTGGCAATCAG	79589
rs768224215	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758757	AAACTAGACCCGTAT[C/T]TCCTGCCATATACAA	79589
rs768227939	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106714360	CAATTCTACAATCAA[C/T]ATGTATTCCTCTTTT	79589
rs768239174	snp	A/G	2.27967e-05	0.00337607	missense	RNF128	GRCh38.p7	X:106773024	AAGTAGGGAAAAAAC[A/G]TGGCCCTTGGGTGAA	79589
rs768259122	in-del	-/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106695130	TATTTAAAAAAACAG[-/T]TTCCAAGTAAATAGA	79589
rs768283040	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766246	AGTAATGGGATGGCT[A/G]GATCAAATGGTATTT	79589
rs768292277	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106785990	TGTTGTTAAGATGTC[A/G]GTTCCCCACCAAACT	79589
rs768292786	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106704469	AGAGCTGGGGAGTAG[C/T]CTGGAAACAACAATG	79589
rs768310757	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731310	TCTTTTGGTCCTCCT[A/G]TGTTTGTTGTACTTT	79589
rs768324230	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750249	ACCCTGAGAGCAGAT[C/T]TCTAAACATTTACTA	79589
rs768399081	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792553	CCTTCTGTGTTCTCA[A/G]TTCTGTCCCCTAATT	79589
rs768445561	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106721649	TATATCTCCCTCAAT[A/G]GTCACAGTGCCTGAA	79589
rs768453795	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784719	AATTGGAAAAAAAAT[A/G]CATATTAATGTCCTC	79589
rs768481881	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106739458	GCAACCATGCCCGGC[A/C]CTCATATTTTAACTG	79589
rs768499803	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106702541	GCAGTCCTCAGTTCA[A/T]AAGTGCTCTTACCCC	79589
rs768511071	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106763549	TCTCGCTCTGTCGTC[A/C]AGGCTGGAGTGCACT	79589
rs768543781	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713086	GGATTTCACCATGTT[G/T]GCCAGGCTGGTCTCG	79589
rs768546297	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786106	AAATGCAAAAGAACT[A/G]GAATGAACAAAACAA	79589
rs768560217	in-del	-/A	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106773960	TGTTATAGTTGCTGG[-/A]AAAAACAAATCCAAC	79589
rs768569457	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106711609	ATAAAAGAAAGGCCC[A/T]ACAGACAGCATGTTG	79589
rs768573318	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106714659	TCAGAACGATTCCAT[G/T]GCAACAGAGCTCCTT	79589
rs768622810	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106787370	ATAATGCATGATTCC[A/G]TTTATATGACATTCG	79589
rs768669349	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751165	TAACATCATATTAAG[A/G]AAAGAGGCACTGGAT	79589
rs768672332	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704249	AACCATCCTAGCTAA[C/T]ACGGTGAAACCCCGT	79589
rs768710748	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106743605	TAGTATTTAAGAAAC[G/T]ACCATTTGTTGAGTT	79589
rs768732397	snp	A/C	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106788334	TTAATATTATATATA[A/C]TATATATAATATATA	79589
rs768751202	snp	A/G	0.00582661	0.0536596	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726892	TGCCAGGGGCGCTAG[A/G]GAACTGCGGAGCGCG	79589
rs768764178	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106751173	TATTAAGGAAAGAGG[C/G]ACTGGATAGGATAGG	79589
rs768764632	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765267	GTTTAAATTAATAAC[C/T]TCAAATAAAGAGAGA	79589
rs768766876	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752416	CCTGGTAATCCAGGG[A/T]ATTCTCCTAGATATT	79589
rs768802300	snp	A/G	4.65219e-05	0.00482274	intron-variant	RNF128	GRCh38.p7	X:106790162	TACTTTACAACTGAT[A/G]ATTATGTTTTTTTCC	79589
rs768813309	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106783737	TTACCTCATGGTTCT[A/G]CAGGCTATACAAGAA	79589
rs768817443	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106776656	AATGACCTTCCATTT[C/T]TAGCTGTAGAAGCTC	79589
rs768856804	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106737684	TACATCTCTTATCTT[C/T]GAAGATTTCAACAGT	79589
rs768873566	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732981	ACATCTATGGATTCA[A/G]CCAACTGAGGAGGAA	79589
rs768907743	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106719163	TAGAAATTATCCAGT[C/T]AGGTTTCTATCAGAA	79589
rs768924961	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106742444	GCAGATTCCCAAGCC[C/T]CACCCCAGACATACT	79589
rs768926948	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106795359	AAATAAGCACATGTA[C/T]GTGAATCAAAAAAGC	79589
rs768928411	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106705959	GAAGGAGTGTGATTT[C/G]ATTGTTTCACAAGGA	79589
rs768971223	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746219	TTGTGAATAACCTCT[A/G]TTTTCTAATATGTTA	79589
rs768983855	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716294	AAATACCACACCAAC[A/G]CAATAACATGGATGA	79589
rs768994497	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106701872	GCAAAATATTTGACA[A/G]CTACATTGTACCACA	79589
rs768998420	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771188	AGTGTCTCCTAGTTA[G/T]GCTACTGAGGGGTCA	79589
rs769042021	snp	G/T	2.30577e-05	0.00339534	intron-variant, missense	RNF128	GRCh38.p7	X:106727368	ACTTCCCCGGGACCC[G/T]CAATGAGGTCATCCC	79589
rs769045516	snp	C/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106710462	GGAGTTTCAGGGATA[C/T]GAAAAGCTGATCTGG	79589
rs769054145	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106782081	GATTCAGACATTTAT[A/G]TTGTATTGAATCAAA	79589
rs769080258	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726186	TACACATGTATGAGG[C/T]TTCTTAGGAGCAGGG	79589
rs769082574	snp	C/G/T	0.000139621	0.00835421	intron-variant	RNF128	GRCh38.p7	X:106790320	TATGAAGAATATATG[C/G/T]CTGGGCTTTGGAGAA	79589
rs769098648	snp	C/T	0.000153955	0.00877232	intron-variant	RNF128	GRCh38.p7	X:106694426	AAGTAATAATTGATT[C/T]ACAAAGAGAGTTAAT	79589
rs769149771	snp	G/T	0.000137615	0.00829388	missense	RNF128	GRCh38.p7	X:106791108	TTACAAGTCCCTGTA[G/T]CCAATGAAATATCTA	79589
rs769236739	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106760175	AAACTAAGTATTTGT[A/G]TAAAACCTTTTGTTA	79589
rs769274092	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106709438	ATCTTCTACTTTAGG[A/C]TTTCATTTCACTGAA	79589
rs769299667	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106737289	TGCAGGTTAGTTACA[C/T]ATGTATACATGTGCC	79589
rs769313494	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771466	TGGCGTACGCCCCTC[C/T]CCCAGCCCCACTGCT	79589
rs769319629	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106750859	GACTGCTTGATTGCT[A/G]AGATCTGTTCCATTT	79589
rs769327533	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106703522	ATAATTAAGAGTCTG[G/T]GCTCTTAATCAGTAC	79589
rs769338267	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106784081	CCTCTACTTCAATTC[A/G]TATGTATATTATATT	79589
rs769357474	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767620	AGAATTTGGGCTGAG[A/T]CGATGGGGTTTTCTA	79589
rs769360871	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747720	TTATTTTACAAATCA[C/T]TGGACATTGAAGGAA	79589
rs769371637	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106711878	CAAATTGATTTGAAT[A/G]AAACAAAAATCAATC	79589
rs769374914	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106729588	CCATATAGGAATAAA[G/T]CCCTAAATATTGATC	79589
rs769375586	snp	G/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106793730	AATTTGGGCTAGTCT[G/T]CTGTTTCCGAGTGAT	79589
rs769391749	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106782880	TTTTCTTCTCTGTCT[A/G]ATTAGATGTCGGGCT	79589
rs769394498	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106700778	ACGTAGTCAATTTGT[A/G]TTTTATTTTTAATAT	79589
rs769411265	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758997	CAAGTAGAAGAGACT[-/A]ACCCATAGAATGGGA	79589
rs769430717	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792810	TTAAAGTTCTTTTGG[A/T]TAAGAACAGTGTCTT	79589
rs769432216	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774899	AATTTATTTAGGGGG[C/T]GGAAGGAGCAGTGAG	79589
rs769432845	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106696224	CTATATTTCAGGCAC[G/T]GTTATAGTGTGTTTA	79589
rs769452645	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714849	TCAGTATAATTCTCG[A/G]GAGATTCATCCAGAT	79589
rs769470702	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106728204	GGTATCCATACCTTA[C/T]GTATATAGTTATCCT	79589
rs769485335	in-del	-/GGCTATCCATAT	0.00581083	0.0535878	intron-variant	RNF128	GRCh38.p7	X:106786356	GATAGCCCTTTGTTG[-/GGCTATCCATAT]GCTATCCATATGCAG	79589
rs769491648	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106719081	AGCTTAATAGGTGAT[G/T]GTGATTACATACTAC	79589
rs769539532	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106737342	TCAAGTACAGTTGTC[C/T]ATTGGTGTCTGTGGA	79589
rs769602082	snp	C/G	2.32466e-05	0.00340922	intron-variant	RNF128	GRCh38.p7	X:106773165	GCAGGAAGCAGGTTT[C/G]TAATGGTCCTTTCTT	79589
rs769615159	snp	C/T	2.29706e-05	0.00338892	synonymous-codon	RNF128	GRCh38.p7	X:106694302	AGAAAGAGGTAATTG[C/T]ACATTTTCAGAAAAA	79589
rs769622958	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730758	AAACATTTACAACGT[C/T]ATGCATAAAACATAT	79589
rs769690353	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106701570	TAGATGATCTCCATA[A/C]ATTAGGTATGGAAAG	79589
rs769694033	snp	G/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106766739	TCCCATTTGTCAATT[G/T]TGGCTTTTGTTGCCA	79589
rs769695030	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752264	TATGCTGGTTTCTGG[C/T]CTAATGCAGCTCAGT	79589
rs769700828	in-del	-/TGT	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106740212	CACATTTTTAGCCTC[-/TGT]TGTTGTTGTTGTTGT	79589
rs769714160	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778955	TGTACCACTATTAAC[A/G]TATATACATTTGCAG	79589
rs769723096	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705453	AATCATTAAATGCCC[A/G]GATACCCTGCATTCC	79589
rs769726998	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731668	TTCCTTGCCTCTCTT[C/T]TGTTTCATTACTATT	79589
rs769741853	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706827	GGCACTTTGCACAAT[G/T]TCTATTCTATAGTAG	79589
rs769761413	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106793026	TTCATGTCGTGTGTC[A/G]CATCATTGGGCTAAG	79589
rs769806448	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106695370	TTTTAGAATTATGAA[A/T]AGGAGAAAATCAAAC	79589
rs769806806	snp	A/G	2.27983e-05	0.00337618	synonymous-codon	RNF128	GRCh38.p7	X:106772995	AAGAGGCATACAAGT[A/G]ACAATGGTCATAGAA	79589
rs769825693	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777633	CCCCAGTCTAGTGAA[C/T]GTGAAGAAAGAAGGA	79589
rs769841261	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106720456	TGGGCTCAAGCAACT[A/C]TCCTGCCTCAGCCTC	79589
rs769849616	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106778919	GAAATTATCTGGAAG[A/T]TTCATTAAGTACCTG	79589
rs769850989	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106795155	ATTCAATTTTGGGCA[C/T]CCTTCCAACTTCCTG	79589
rs769852495	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106743876	CAACAATGATAGACT[A/G]GATTAAGAAAATGTG	79589
rs769861590	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741207	CAATAGCATATCTTA[A/T]TTTTTTCCTCAGTAT	79589
rs769910027	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106742814	AGTGCTAGTTTCACT[A/T]AAGAATGCCCTTGAT	79589
rs769929267	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106761606	TACAGCCATAAAAAA[-/A]GAATGAGATCATGTA	79589
rs769945461	snp	A/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726007	TAGTTAAGGTCATGA[A/T]TAGCGCAGGAACATC	79589
rs769948599	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106697152	AATAAACCTTTTTTG[C/T]AAGTGGGGAAGACTA	79589
rs769948985	snp	C/G	5.24576e-05	0.00512114	intron-variant, missense	RNF128	GRCh38.p7	X:106727002	TCCTGCTGGCCCTGA[C/G]TCCGCAGGCACCCGG	79589
rs769949159	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106707344	AAACTATGCCAAAAT[A/G]TGCCTTCCTCTAACT	79589
rs769973935	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717624	TTATTCTAATGAATA[A/G]AGCAGATGAATTTTA	79589
rs769980481	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790008	TACATTTAAAAGTAC[C/T]GTATTATGGAATTTC	79589
rs769997572	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106758335	AAGTTTCAATTTTAT[A/T]AAAAGGTTCATACTA	79589
rs770000429	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106708685	CAGCAGTGCTTCTTT[A/T]TGGCATCATTTTAGT	79589
rs770011372	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106722243	GATGGGATGCTTGGT[A/G]AGGTAGTGAGCTCTG	79589
rs770025667	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106781713	GCTATTGAAAATACT[C/G]AAATTTTCTTTTAAA	79589
rs770043961	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106795379	ATCAAAAAAGCAATT[A/T]TAAATCAATATAATA	79589
rs770048799	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106735325	CCTTTTTTGAAAGAA[A/G]ATAGTCCTTGAGCTC	79589
rs770051021	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106761223	CCAATCCAAATCACA[A/G]TGCAATACCATCTCC	79589
rs770055831	in-del	-/TTTTAGGATG			utr-variant-3-prime	RNF128	GRCh38.p7	X:106795731	CTGTGTAAATAGAAA[-/TTTTAGGATG]ACTTGAACCATTAGT	79589
rs770137336	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106719230	ACTGCCCATGGGCAT[-/T]TTTTTTTTTTTGAAA	79589
rs770157229	in-del	-/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702097	ACAAATGCCCAGGTG[-/C]CCCCCTCCCCTGGGT	79589
rs770176124	in-del	-/TT	0.112567	0.208835	intron-variant	RNF128	GRCh38.p7	X:106788396	TATATATAATATATA[-/TT]ATATATAATATATAA	79589
rs770214039	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772504	TCATCTTATAAATTG[G/T]GAAATATTTCTGTAT	79589
rs770223385	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765859	TTATCTCCTAATGCT[A/C]TCCCCCCCAGCCCCC	79589
rs770241894	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749056	TTTCTCAGGCAAAAG[A/G]TGATATTTTAATCTA	79589
rs770243874	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106746051	AGGAAATGTTTGTTA[C/T]GTTGGAACTCTTTAC	79589
rs770264367	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771956	ACCCAGATTAGCACC[C/T]TAACTTAATATCAGT	79589
rs770279320	snp	G/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725461	TTGAGGGGAGTAATT[G/T]ATCAGAAATTTAACA	79589
rs770285263	in-del	-/A	2.40422e-05	0.00346706	intron-variant	RNF128	GRCh38.p7	X:106773189	CTTTCTTCCACTATT[-/A]AAAAAAATTTACTGT	79589
rs770313898	snp	C/T	2.31254e-05	0.00340032	intron-variant	RNF128	GRCh38.p7	X:106790301	AACATTAATATGTTA[C/T]TTATATGAAGAATAT	79589
rs770314042	snp	C/T	2.28308e-05	0.00337859	synonymous-codon	RNF128	GRCh38.p7	X:106694191	ACCAGTGGCTAATGC[C/T]ATGGGAGTGGTAGGC	79589
rs770321867	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106743275	ACTTTTATCTACTAT[A/G]TAAGCATAACTTCCC	79589
rs770325248	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106721946	AAACATATAGTAAAT[A/G]CTCAATGAACAGTAG	79589
rs770353348	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702928	TATTCAACAGTATAG[G/T]AATGTTAATAGTCAT	79589
rs770363339	snp	A/G	2.34137e-05	0.00342145	intron-variant	RNF128	GRCh38.p7	X:106790148	AGGTAAAGTGTTGCT[A/G]CTTTACAACTGATAA	79589
rs770410675	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106749236	TGAACATGACCACAT[C/T]TATATTGCTTATAAT	79589
rs770413626	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106770344	CTGAAGAGTATTTTC[C/T]GACGTGGTTCCATTC	79589
rs770442738	snp	G/T	0.000529661	0.016265	intron-variant, missense	RNF128	GRCh38.p7	X:106726917	AGCGCGCGCGCCATG[G/T]GGCCGCCGCCTGGGG	79589
rs770465829	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747960	CAGGCTAGCATAGTG[C/T]CAGGCATGTGTGTAG	79589
rs770465935	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761470	TCTACCATAAAGACA[C/T]ATGCACATGTATGTT	79589
rs770467592	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106724654	CTTGTGTTGTTTTCT[A/G]CCTAGAAAAGTTTAC	79589
rs770482953	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106771729	TGGCCTGCCCTGCTC[C/T]GTGGGCTGTACCCAC	79589
rs770485344	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106783809	CTACCTATCATGGCA[G/T]AAAGGAAAGGGGAAG	79589
rs770497324	in-del	-/TA	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106738789	TAATATAATTGTCTC[-/TA]TGTCATAGGGTTATT	79589
rs770518776	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106698996	GATGCCTTCCTCATC[C/G]TCGCTCCCACATCTC	79589
rs770523320	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106703042	GACATATATTCTCAG[C/T]ATGACCTAGCTAATG	79589
rs770554444	in-del	-/T	0.247056	0.249983	intron-variant	RNF128	GRCh38.p7	X:106712882	AGTAGATAAAGTTAC[-/T]TTTTTTTTTTTTTTT	79589
rs770564523	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106758100	TGCAGAATGCAAAAT[A/C]AACATATATAAATCA	79589
rs770564539	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767771	ATAGGAGTGGTGAGA[A/G]AGGGCATCCCTGTCT	79589
rs770565728	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106700506	TTCTCTTTTATATGT[A/G]AAAAGATGGACAAGT	79589
rs770615224	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106749059	CTCAGGCAAAAGATG[A/G]TATTTTAATCTATCT	79589
rs770619071	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726401	TGGCACCGTAAGCCC[A/G]AAATGTCCTTTAGGC	79589
rs770659029	snp	C/T	0.000106283	0.00728903	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693983	AAACATCTTAAATTT[C/T]ATACTCAAATGAATG	79589
rs770685023	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106753165	AATAATATTATAACA[A/C]TGTAGTTGTGGTGTG	79589
rs770731808	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705742	CTTATGTATAGCAAG[A/G]TTAGCTGCAGTTGGA	79589
rs770756712	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106735005	CCACCTTGGAGCCCT[A/G]TGGGCAAAGTGGAAC	79589
rs770841525	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106742243	AAACAAAATAATTCT[A/G]TTGGCAGAGTTTTTC	79589
rs770843296	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731845	TTTCAGTTCCTGTGT[C/T]TTCTCATGGGAAAAA	79589
rs770844573	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696360	ATTTTTTCCTTCCTA[G/T]AAATTTCCTTTATAT	79589
rs770848434	in-del	-/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762647	TTATTTTAGGCTCAA[-/G]GACACATGTGTTGGT	79589
rs770884311	snp	A/G	4.56199e-05	0.00477576	synonymous-codon	RNF128	GRCh38.p7	X:106772971	CACAAAAATTCTGCA[A/G]TCTATTCAAAGAGGC	79589
rs770890216	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106793983	TACACAAATGTCCTG[A/G]TACTTATCATACTTC	79589
rs770894697	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106741390	ATGGCATGTGTACCA[A/G]CATCTGAATGGAAGT	79589
rs770910374	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106792654	ACCCAAGAAGTTAGG[C/G]GAGCCCAGTATAACT	79589
rs770922558	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768609	ATTCTTCTCTCTTTT[A/C]TTCTTTATTTGTCTT	79589
rs770926113	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106705802	GTACCATTTCAACCA[C/T]ACACACAGGCAAATG	79589
rs770997178	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106734583	ATAGGTATTTCCTGG[G/T]AATAAATAATTTTTG	79589
rs770998471	snp	A/G	0.00105904	0.0229869	downstream-variant-500B	RNF128	GRCh38.p7	X:106797231	CAAGAGCAGGAGGAA[A/G]AGAGAGAGAAGCAAG	79589
rs771028080	snp	A/G	0.000125471	0.00791956	intron-variant, missense	RNF128	GRCh38.p7	X:106726957	CCTGCCGCGGTGGCT[A/G]CGGCTTTTCCAGATT	79589
rs771045094	in-del	-/TATATAA			intron-variant	RNF128	GRCh38.p7	X:106737436	ATGGCATAGTATTTG[-/TATATAA]TATATGCATCTCCTC	79589
rs771092844	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106742970	ATATGTATTTCTGTG[A/T]CATGAAATGGGAAGT	79589
rs771103761	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106724031	CCTATCACACAGTTC[C/T]ACCTGGTTACATCAT	79589
rs771107830	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106777202	TGAACTAAAAACTCC[C/T]CACAGTGTGATACCA	79589
rs771145387	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714035	AAAAAAATTAGTCGG[A/G]TGGTGGCAGGCACTC	79589
rs771145853	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106724292	CCTGTCTATCCAAGC[C/T]ATCTTCATCTCTCAC	79589
rs771156194	in-del	-/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106709111	CAATTATAGAACTTG[-/C]CTACTTCAAGCAAGT	79589
rs771156783	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723238	GCTTTATGTATGTGT[A/G]TACACATGTGCATGC	79589
rs771156994	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106778724	GTTCCCTGGGCAGAG[A/T]TATGCCACACATTTC	79589
rs771157704	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106785417	ATCCTGGATTATCCA[C/G]ATAGATTCAAAATAT	79589
rs771158825	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735964	TCTTTGTATTTTTGT[G/T]TTTTTTTCCCGTAAG	79589
rs771188190	in-del	-/C	4.83238e-05	0.00491524	intron-variant	RNF128	GRCh38.p7	X:106727443	AGACCTCTGCCATGG[-/C]CAGTTTCTCTTATTT	79589
rs771192626	in-del	-/AGAC			intron-variant	RNF128	GRCh38.p7	X:106748813	CACAAAAATACAGTT[-/AGAC]AGAAGAAATAAGCTC	79589
rs771206732	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106763728	AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCAT	79589
rs771240377	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106713983	GATCGAGACCATCCT[A/G]GCTAACATGGTGAAA	79589
rs771247684	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106707081	TTGCCTTTTTGCCTA[A/T]TTTTATGTATTCTTA	79589
rs771248841	snp	C/T	0.000529661	0.016265	missense	RNF128	GRCh38.p7	X:106790214	AAGACATGTGTTGAC[C/T]CATGGCTGTTAGAAC	79589
rs771278640	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106785905	CTGTAAAACACTAAT[C/G]AAAGAGATAAATCAA	79589
rs771285482	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106695783	ACTTAGAGATCCTGA[A/G]TACTCTGGGTTTCCT	79589
rs771285592	in-del	-/TA	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106789086	ATATATACTATATAG[-/TA]TATATAGTATATATA	79589
rs771292959	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728302	ATAGTTTTTAAGAGC[G/T]GGGCCTCAAGTCAGA	79589
rs771293690	snp	A/T	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693481	TGCCATAGCAATTAA[A/T]CTCATGGATCTTAAC	79589
rs771352034	snp	C/T	2.50257e-05	0.00353726	intron-variant	RNF128	GRCh38.p7	X:106787875	CTGTAGTTTAATGTA[C/T]TTTTTCTTATCTGTC	79589
rs771360743	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106763804	GTGGGCCACCACGCC[C/T]GGCCAATTCAGGTTT	79589
rs771391948	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106779475	TTTATTCATCTAAAA[A/C]ATTTGAACTCATAGA	79589
rs771481969	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106697436	TCAACAAGAAAATGT[A/C]AAGGCTTAATTGAGA	79589
rs771489954	snp	A/C/G	9.96447e-05	0.00705789	missense	RNF128	GRCh38.p7	X:106694019	TGAACCAGGAGAATA[A/C/G]GTCCAGTTTTTTTTG	79589
rs771497614	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106707799	TTAAAAAGGCAAATG[A/G]TCCCAGGAAAAAAAA	79589
rs771558502	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106787775	CCTTTGGGAACTTTA[C/T]AGTTACATAATCATT	79589
rs771563495	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106739262	CATCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	79589
rs771572334	snp	C/G/T	0.000273972	0.0117011	synonymous-codon	RNF128	GRCh38.p7	X:106694200	TAATGCTATGGGAGT[C/G/T]GTAGGCATCCCTAAG	79589
rs771580448	snp	A/C/T	0.00105918	0.022993	intron-variant	RNF128	GRCh38.p7	X:106717772	GTTCCTTAATTTGTA[A/C/T]ACTTAATGTAAAGAT	79589
rs771588664	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106791881	AAAAATTATTTTCCC[C/T]TTCTTTTACCTCAAT	79589
rs771614186	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106741711	ATTAAATCAAAATTC[A/G]AATTATCACTAAATA	79589
rs771622177	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717659	AAATCACTGAAACTC[C/T]AAAATAGAAAATTAT	79589
rs771625736	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106697754	GGATAATTTCAGTTT[A/G]AGAATAGCTTCCACT	79589
rs771629901	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106703357	GAGCATTCTTCTCAG[C/T]GTAATCATCCCAACA	79589
rs771638788	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765911	GTGTGATGTTCCCCA[C/T]CCTGTGTCCAAGTGT	79589
rs771664653	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750207	ACCATGGAAACTGGC[A/G]CACACTACACATTAG	79589
rs771667233	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106734874	TCCTCTTCACTGCAC[C/T]GGGGTTATTTTATGG	79589
rs771667305	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106715666	GAGAGCTTTTAGCAG[G/T]TATCAGATTCAATAA	79589
rs771701186	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106777114	TCTGATATGGTGTAA[A/T]ACTGGTATTGTTAGT	79589
rs771709094	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106761564	CTGAATAAAGAAAAT[A/G]TGGTGCAAATACACC	79589
rs771710690	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106767529	TTGTCTGTTATTGGT[G/T]TATAAGAATGCTTGT	79589
rs771723145	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740069	TGCACATAAGAAGAA[A/G]CACCAATTTCAATAA	79589
rs771725083	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728485	ATGCCTTAAAGAGTT[C/T]AGTGCAGTAAAGCAC	79589
rs771731505	snp	A/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106733571	CTGTACATAGGCATA[A/T]CTTTGTATTCTACTT	79589
rs771764065	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106744614	ACAGGCACGTGCCAC[C/T]ATGCCCAGCTAATTT	79589
rs771804581	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106705677	ATAATTTTTCAACTG[A/G]TTTTTTTAGCCTCAT	79589
rs771814902	in-del	-/GT	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794977	TGTAAAACAATGTCA[-/GT]AACTAGTGTACAGTT	79589
rs771836263	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751474	GGTCCTAAATAAATA[C/T]GAAAGGCAGTCTAGA	79589
rs771855945	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106706800	ATTAAATTACATAAT[G/T]CATATAAAGAAGGCA	79589
rs771865526	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106779390	GTGTGTGTGTGTGTG[-/T]TGAGGATACTTAAGA	79589
rs771893227	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106752964	AGAACTGATCAAGCA[A/G]AAGAAAAAAGTATTG	79589
rs771935104	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769498	TCTTTTGATCTTTGT[G/T]GGTTTAAAGTCTGTT	79589
rs771955535	in-del	-/A			downstream-variant-500B	RNF128	GRCh38.p7	X:106797028	TTAACTATCTGTATT[-/A]GGATGTTTCTTGTGT	79589
rs771976769	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106739316	AGGAGTGTGCTACCA[C/T]GTCCAGCTAATTTTT	79589
rs772023458	in-del	-/A	0.223598	0.248602	intron-variant	RNF128	GRCh38.p7	X:106706386	ATGCTTCCTTATGTG[-/A]AAAAAAAAACAAAAA	79589
rs772025958	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106695725	TTCTGATAAAACTTA[A/G]GAATTAAATCTGTTC	79589
rs772047874	snp	C/T	2.29474e-05	0.0033872	missense	RNF128	GRCh38.p7	X:106694082	TTACAGCATCTTTTT[C/T]AATGAGTGCCTATGT	79589
rs772061591	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768696	GATTTTTTGAAGGGT[G/T]TTTTGTGTCTCTATC	79589
rs772062057	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106698036	GGATATGTTTACCAT[A/G]TTCTTAAGTAAGTAT	79589
rs772063886	snp	G/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106712975	AACCTCTGCCTCCTG[G/T]GTTCAAACGATTCTC	79589
rs772069845	snp	A/T	4.60989e-05	0.00480076	missense	RNF128	GRCh38.p7	X:106795694	ATCAAGAGACTGCTG[A/T]TCGAGAAATTAAATC	79589
rs772081684	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762471	GGCATGCACTGCCAC[A/G]CCTGGCTAATTTTGT	79589
rs772107820	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763884	TGAAGCACAGCATTG[C/T]TGCTAAGATGTATAC	79589
rs772162432	snp	A/G	6.86358e-05	0.00585774	missense	RNF128	GRCh38.p7	X:106791117	CCTGTATCCAATGAA[A/G]TATCTAATAGTGCCT	79589
rs772169136	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106720837	GTTGTGAAAATCAAA[C/T]GATAACATTAATATA	79589
rs772182605	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106732463	TTGCCTTAAACACTC[A/G]AGAACTCTAATGCCA	79589
rs772205303	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770829	TGGAGGAGAAGAGGC[A/G]CTCTGATTTTTAGAA	79589
rs772209021	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106764919	TGTGATTTTAGTGCC[A/G]TAGCTAAAAATTTAA	79589
rs772215670	snp	A/G	4.662e-05	0.00482782	intron-variant	RNF128	GRCh38.p7	X:106790324	AAGAATATATGCCTG[A/G]GCTTTGGAGAAAATA	79589
rs772241546	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786510	GAAATTTTTAGAACA[A/G]AACGTTAAAGAAAAA	79589
rs772286563	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106700513	TTATATGTGAAAAGA[C/T]GGACAAGTTGAAATG	79589
rs772298610	in-del	-/GAGTAGTACAGAGA	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704731	GTAGAAGAAAGTAAT[-/GAGTAGTACAGAGA]GAGGAGCACAGAAGT	79589
rs772304315	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106775393	TAATAAGGTTTATAA[A/G]GAACTTTGTCTGGTG	79589
rs772336327	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714919	GTGATATTCCATGGT[A/G]TAGATGTACCACAGT	79589
rs772365620	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106774661	TTCTTATTACCTTCA[G/T]TGCTTCTGCCCCAGT	79589
rs772378443	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106721813	TGGAATCCTTCTTCT[A/G]TTCCTAGCTATATGG	79589
rs772384922	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106728030	GCAAAACAGGTGACT[A/G]ACGTTCTTGAAAAAG	79589
rs772397408	in-del	-/TC	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710323	GCACCTGTTATATAT[-/TC]TGTTAAAATGGTATA	79589
rs772465863	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106745317	GGGTCACATTCCCTG[C/T]GATACACCCTCCCTC	79589
rs772496929	snp	C/T	3.3741e-05	0.00410723	intron-variant	RNF128	GRCh38.p7	X:106694452	TTAATGTCCGTTTAT[C/T]TTAGAATGGTATTTC	79589
rs772498083	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106712137	TTCAGAGTCACGTCT[C/T]TATATGTCTGAAGAG	79589
rs772512041	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106782402	GTGTGTGGGCCAGGG[C/T]CAGGACCCTGTAGGC	79589
rs772543774	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770175	CTCTGGCTGCCCTTA[A/G]CATTTTTTCCTTCTT	79589
rs772576149	in-del	-/ATCTATCTAC			intron-variant	RNF128	GRCh38.p7	X:106697910	GGTGAGTATATCTCT[-/ATCTATCTAC]ACACAAACATATATG	79589
rs772608217	snp	A/G	0.00528398	0.051128	intron-variant	RNF128	GRCh38.p7	X:106755965	ACAGAGAGCCAAATC[A/G]TGAGTGAACTCCCAT	79589
rs772635033	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735378	TTAAATGTTAACTTG[A/T]CATTTCAGACAAAAT	79589
rs772652035	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106710735	GCACTCCAGCCTGGA[C/T]GAAAGTCTGTCAAAA	79589
rs772656537	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106697803	GCCTAATAATTGGAG[A/G]TAAACTTCTAACTCA	79589
rs772661424	in-del	-/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106699390	AGCTTTTGTACTTGC[-/T]GCCTCCTCTGCCTGA	79589
rs772706402	snp	A/G			utr-variant-5-prime	RNF128	GRCh38.p7	X:106693862	ATGTATCCAGAGGTT[A/G]TGTTGCTAGAGGTGA	79589
rs772708129	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106746542	AAGGAAATGAAAGAA[G/T]TTGGCCACCAGCAGG	79589
rs772713217	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760215	TTTACTTTTATGGAA[C/T]ATCTAATTCCTAAAA	79589
rs772724649	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106763559	TCGTCCAGGCTGGAG[A/T]GCACTGGCACGATCT	79589
rs772727194	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106747804	TTATTATTTTCTACT[A/G]CTGGCCATAATAGTA	79589
rs772753936	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106767622	AATTTGGGCTGAGAC[A/G]ATGGGGTTTTCTAGA	79589
rs772805412	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106744637	GCTAATTTCTTGTAT[C/T]TTTAGTAGAGACGGG	79589
rs772834680	snp	A/G	4.56991e-05	0.0047799	missense	RNF128	GRCh38.p7	X:106795621	GAAGCAAATTCTGTG[A/G]CAGTGGATGTTATTC	79589
rs772856226	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106700788	TTTGTGTTTTATTTT[C/T]AATATTAACAAAGTT	79589
rs772858509	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106746507	GATTAGACAAAAACC[A/G]TAATATCATTAGCTT	79589
rs772890747	snp	A/G	0.00422943	0.0457911	intron-variant	RNF128	GRCh38.p7	X:106737534	AAATAGTTGTTAATA[A/G]CATTGTTTAGGGAAT	79589
rs772913241	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106716682	CTTGCCAATCATTTA[C/T]TTGCACTTCAAGTGA	79589
rs772926393	snp	A/C	0.000528999	0.0162548	intron-variant	RNF128	GRCh38.p7	X:106785183	TTAAAGCAGTGCTAC[A/C]AAGCCATTGTTCAGG	79589
rs772939569	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772032	CTTCTTTTGCTTAAG[A/T]TTATTGGTCTCAGGT	79589
rs772946520	snp	A/C	0.0110639	0.0735497	intron-variant	RNF128	GRCh38.p7	X:106704293	TACAAAAAAGCCAGG[A/C]GTGGTGGCTGGCGCC	79589
rs772960767	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792911	TTAAACCAGATTTAA[-/T]TTTGTCTGGGATTAC	79589
rs772966491	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106717245	TATATTGTATTCAAT[A/G]TGCAATGAAAAGTGA	79589
rs773041789	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771530	CAGTGAGCGAGGCTC[C/T]ATGGGCATGGGACCC	79589
rs773042801	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106777160	TATATAAATAAATCA[C/T]ATGGTAATCAAATAT	79589
rs773053872	in-del	-/AGAT			intron-variant	RNF128	GRCh38.p7	X:106759747	ATTTTAAACAGTTGG[-/AGAT]AGATATCAGAAGGAT	79589
rs773062210	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783648	CCATTATATTCCACA[C/T]ATGTATTAGTCGGGT	79589
rs773075857	in-del	-/C			intron-variant	RNF128	GRCh38.p7	X:106768917	TCTGGTATGTTGTGT[-/C]TTTGTTCTCATTGGT	79589
rs773077752	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775016	ACCAGCATATGGTAA[C/T]AAGTGATGGTTATCT	79589
rs773116798	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767621	GAATTTGGGCTGAGA[C/T]GATGGGGTTTTCTAG	79589
rs773137829	snp	A/G	4.61297e-05	0.00480237	intron-variant, missense	RNF128	GRCh38.p7	X:106727370	TTCCCCGGGACCCGC[A/G]ATGAGGTCATCCCCA	79589
rs773152733	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106707705	TTCTCCTCCCTATTA[A/G]CATGCTGTCTAAAAT	79589
rs773170301	snp	C/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106766799	TTGCCCATGCCTATG[C/G]CCTGAATGGTATTTG	79589
rs773233917	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106732490	GCCAGAAGGGTCACA[A/G]GATTCACTAGAAAAG	79589
rs773264536	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106791371	TACTTAAAATAATGC[C/T]GTGAAGGATGCACCC	79589
rs773276486	snp	C/T	2.62612e-05	0.00362352	intron-variant	RNF128	GRCh38.p7	X:106694453	TAATGTCCGTTTATC[C/T]TAGAATGGTATTTCC	79589
rs773283929	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106721857	GCTGTAATTCTCTCT[A/G]GGCCAGTTTTCCCTT	79589
rs773285844	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106715802	CAAGTTGTATACCTA[C/T]CTGGACAGAGAGCTG	79589
rs773294806	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106744079	GGACACAGGAAGGGG[A/G]ACATCACACACTGGG	79589
rs773295020	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106733104	TTACATAGCATTTAC[A/G]TCATATTAGGTATTA	79589
rs773316137	snp	C/G/T	0.000161476	0.00898424	missense, stop-gained	RNF128	GRCh38.p7	X:106795696	CAAGAGACTGCTGTT[C/G/T]GAGAAATTAAATCTT	79589
rs773322885	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106751540	GTTCTGTGCTGGGCT[C/T]AGAACCAGAGGACTT	79589
rs773333989	snp	A/G	2.3677e-05	0.00344063	missense	RNF128	GRCh38.p7	X:106694345	GGCAGAAGAAATGCT[A/G]ATGCTGTTGTGATTT	79589
rs773337153	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698341	TCCAACGAAGTGGAT[G/T]AGAGTCAAGTGTGCG	79589
rs773357667	snp	C/G	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106769611	TCCCTTTATTTTGAG[C/G]CTATGTGTGTCTCTG	79589
rs773371960	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106795394	ATAAATCAATATAAT[A/G]ATGCCATATGTGCTT	79589
rs773376509	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768986	GTACCCATTAGTCAT[G/T]CAGGAGCAGGTTGTT	79589
rs773382691	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706848	TCTATAGTAGACAGT[A/G]AAAACTACGGTAGTA	79589
rs773409024	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106720910	TAAAGTTATGGATAT[A/G]AAAAGATTGTTCTTA	79589
rs773416742	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787595	GTATGTGAATTATAC[A/C]TTAATTTTTTAAAAA	79589
rs773423415	snp	A/G	0.00422943	0.0457911	downstream-variant-500B	RNF128	GRCh38.p7	X:106797099	AAACAGGATTAATTG[A/G]CTCATGGTTTTATAA	79589
rs773437178	snp	A/G	2.44735e-05	0.00349802	intron-variant	RNF128	GRCh38.p7	X:106773203	TAAAAAAAATTTACT[A/G]TTCTAATTGTAGTTT	79589
rs773452613	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106705716	CAGCCAGCATCTAAA[G/T]GCTCAGTTAACTTAT	79589
rs773454849	snp	A/G	2.41633e-05	0.00347579	intron-variant	RNF128	GRCh38.p7	X:106791015	GAAGTGATATGTCGA[A/G]GAAAAGCGTGTACAC	79589
rs773478312	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765554	TAGAAAAAAGGGGCA[C/T]TCTCTGGCAAAATTA	79589
rs773492001	in-del	-/CCT			intron-variant	RNF128	GRCh38.p7	X:106702473	AGAACAATGCCTGAG[-/CCT]ATATAAAGTAGGCTA	79589
rs773508377	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106715510	AATTGGCTATCTGCT[-/A]AGACAGATGCCCTAA	79589
rs773509109	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106738546	GAAACGACTATATTA[C/T]CTTCCTTCTCCCTGG	79589
rs773564269	snp	C/T			utr-variant-5-prime	RNF128	GRCh38.p7	X:106693891	GAGATCAGTTACCTA[C/T]GTGCAACTGAAATTT	79589
rs773618970	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761663	CACATAGGACTATTG[C/T]CATTCACTTTTCTTA	79589
rs773639816	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106753687	CATTAAAAAGCCCCA[A/G]CTAGCTGCCATCCTT	79589
rs773681339	snp	G/T	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106691906	TATTAAATGAAAAAC[G/T]AATTTAAAAATATAT	79589
rs773684407	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106782492	ATCAAAAGACAGATG[A/C]GTTATGGATGGTTGT	79589
rs773704230	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106742832	GAATGCCCTTGATGA[A/G]TCAAAAAGAATAATT	79589
rs773713508	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702279	TAAAATCAAAGAACA[-/T]TTTGAAAGCATCTAA	79589
rs773713794	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777645	GAATGTGAAGAAAGA[A/G]GGATGGAGGCCTTCA	79589
rs773751968	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106737685	ACATCTCTTATCTTC[A/G]AAGATTTCAACAGTC	79589
rs773757769	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106761928	AGAACTTTTTTATTT[G/T]GGGCAGACACTGTCT	79589
rs773762892	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754625	ATAAAACTAAGTCAA[C/T]AATAACAGAAACTTT	79589
rs773763344	in-del	-/T	0.11768	0.212112	intron-variant	RNF128	GRCh38.p7	X:106788625	ACTCTATATTATATA[-/T]ACTATATAATATAGT	79589
rs773772629	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106711989	CTCTTTAGTGGCTAC[A/G]TGCTCATGGGAGTAA	79589
rs773774111	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106783882	TTTTAAACAACCAGC[A/G]GGAACTGAGAACTCA	79589
rs773779237	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106739327	ACCATGTCCAGCTAA[A/T]TTTTGGATTTTAGTA	79589
rs773795376	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106695750	CTGTTCTAAGGAACC[A/C]ACTTGCTATACATTT	79589
rs773810998	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106763786	AGTGCTGGAATTAAA[G/T]GCGTGGGCCACCACG	79589
rs773820554	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106784603	AGAATTAAATGACTC[A/G]TGCAGGGTTATTCAT	79589
rs773844520	in-del	-/TTAAA			intron-variant	RNF128	GRCh38.p7	X:106761059	AAATCTTTAAGGAAC[-/TTAAA]TTAACAAGCAAAAAT	79589
rs773869434	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749261	TATAATAAATGGCTA[A/C]CTTTACATCTGAATG	79589
rs773878334	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716534	GGTTAAATGACTGTA[C/T]ATATTTGTAAAAACT	79589
rs773908362	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106786045	AATAAAAATCCTAGT[A/G]TAAATCTTTTATAGA	79589
rs773932531	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784499	TCTTCATTAAGCAAT[C/T]GTGGTTATAAGCACC	79589
rs773943071	snp	C/T	2.4214e-05	0.00347942	intron-variant	RNF128	GRCh38.p7	X:106773198	ACTATTAAAAAAAAT[C/T]TACTGTTCTAATTGT	79589
rs773947592	in-del	-/TATATATAC	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106789096	ATATAGTATATAGTA[-/TATATATAC]TATATACTATATATA	79589
rs774006362	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106767285	TGGGGATGGCATTGA[A/G]TCTATAAATTACCTT	79589
rs774015393	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106765793	ACATATGTTTACATG[C/T]GCCATGTTGGTGTGC	79589
rs774024471	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692728	CTATTTTTTTATTTT[C/T]GGTTGTCCTGTCCCC	79589
rs774074542	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106697683	TACAGAATGTCCTTA[C/T]TCTTGAGTCCAGTCT	79589
rs774086987	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106703165	AAAGAGAAATGAAAA[A/T]TTCCTTAATAATTCA	79589
rs774087336	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783829	GAAAGGGGAAGCACG[C/T]GTGTCACAGGGAGAG	79589
rs774166715	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696397	TATTCAGTGATGCAG[C/G]TGACAAACATAAGGA	79589
rs774177041	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792949	TAGTTTAAGAATCTT[A/G]CGTATTAGCCATTGA	79589
rs774177730	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106705772	AGGCCACAGTAGTTA[C/T]ATCTGAGAAATGTAG	79589
rs774186514	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772666	TAATCTGAGGAGGGG[A/G]AGGTGTTTGTTGTAT	79589
rs774186607	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765673	TTTTGTATTTAAATT[A/C]TAGTCTAAAAGTCCT	79589
rs774187189	snp	A/C	4.93986e-05	0.00496959	intron-variant, missense	RNF128	GRCh38.p7	X:106727007	CTGGCCCTGAGTCCG[A/C]AGGCACCCGGTTCCC	79589
rs774219095	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732833	TTTTGATCTTTTAAA[A/T]ACTACACCAGCATTA	79589
rs774223466	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794004	ATCATACTTCTACCC[A/T]CTACTTTTAGCAATC	79589
rs774231517	in-del	-/TTCAAAGGGAATGCTTCCAGTTTTTGCCCA	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106767797	TGTCTTGTGCCAGTT[lengthTooLong]TTCTGTATAATATTG	79589
rs774243981	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106774396	TTTTGTCTTTTGTAT[A/G]CTCAAGGACATCACT	79589
rs774263738	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106748018	AATTAAGAGTACTGT[C/T]TGTCTTCTGTATAAC	79589
rs774273460	in-del	-/TG			intron-variant	RNF128	GRCh38.p7	X:106719241	GCATTTTTTTTTTTT[-/TG]AAACAGAGTCTCTGT	79589
rs774287570	snp	A/G	4.5672e-05	0.00477848	missense	RNF128	GRCh38.p7	X:106694201	AATGCTATGGGAGTG[A/G]TAGGCATCCCTAAGA	79589
rs774324661	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770141	ATGGGCTTCCCTTTG[A/T]GGGTAACCCGACCTT	79589
rs774328118	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106749618	AGTTTTTAAACATAA[A/G]TATGAGGCCAGCCAT	79589
rs774342754	snp	A/G	2.32062e-05	0.00340625	intron-variant	RNF128	GRCh38.p7	X:106790166	TTACAACTGATAATT[A/G]TGTTTTTTTCCTGAA	79589
rs774344167	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731914	TTTTTTTCCTAGTAT[A/G]CAGTTCTTCCTCCAT	79589
rs774381789	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774170	TGTTGGATAACCATA[C/T]GTGTTCCTTTCCCTT	79589
rs774385364	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106751210	AGTCATTAATTTCTT[A/C]CACCACCCCTCCCTC	79589
rs774401078	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783022	AATTTTTTTAGTTCA[C/T]AATTATGTCCCAAAA	79589
rs774418256	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106739174	TCTTTCTGACTTTTT[G/T]TTTGAGACGCAGTCT	79589
rs774452634	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106721038	TGTTTCCTAATGGTT[A/G]TATACTAACTTGAGC	79589
rs774459561	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106714072	AGTCCCAGCTACTGG[A/G]GAGGCTGAGGCGGGA	79589
rs774521118	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106762660	AGGACACATGTGTTG[-/A]GTTTGTTGTATAGGC	79589
rs774538429	snp	A/G	0.00581083	0.0535878	downstream-variant-500B	RNF128	GRCh38.p7	X:106797279	ATAAGCAGATCTTGC[A/G]TGAACTGAGTGAGAA	79589
rs774544672	in-del	-/TC	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699341	CAGCGACTCTGGTTT[-/TC]TCTCTGTTTTTTAAC	79589
rs774581018	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754694	CTGAATGACCAGTGG[C/G]TTAATGTAGAAATTA	79589
rs774588237	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106701966	TATATAACATGTTAC[A/G]CCTGGAAAATAACTC	79589
rs774588306	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106720769	ACTTCATTTTTCTGA[G/T]TCTCATTTTCCTCAT	79589
rs774632597	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106698404	AGAGTAGTGAAGTGC[A/C]TGAAAAGGAAGGGTT	79589
rs774642346	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728337	GGTTTAAATTCCTAC[A/T]CTGTTGCTTACTAGT	79589
rs774644216	snp	A/C			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726245	AAGAAAGGGTAACAG[A/C]GCGCTTTTCCTGCCC	79589
rs774672113	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777689	CCTCTTAATTAAGAT[A/G]AAATTTATTTTCTCT	79589
rs774681352	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106759066	TAACCAGAATACTTA[A/T]GGAGCTGAAATCACT	79589
rs774697585	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106709450	AGGCTTTCATTTCAC[G/T]GAACTGTGCCATTTA	79589
rs774725409	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106755766	AAGGAAATAAAGGGT[A/G]TTCAATTAGGAAAAG	79589
rs774813013	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733868	AACACACCCGGCTAA[G/T]TGTTATAGTTTTAGC	79589
rs774838302	snp	A/C	0.00105904	0.0229869	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693597	CTTTCAGCCTTGTCA[A/C]GTGGGATTCCCCAGA	79589
rs774854829	snp	A/G	2.27975e-05	0.00337612	missense	RNF128	GRCh38.p7	X:106773005	CAAGTGACAATGGTC[A/G]TAGAAGTAGGGAAAA	79589
rs774895139	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106745135	GGACTCCATCTACCA[A/G]AGAATTTTTGTGCTA	79589
rs774902905	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106779477	TATTCATCTAAAAAA[C/T]TTGAACTCATAGATG	79589
rs774912490	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106779904	ACAGCTACATGGCTC[A/G]GACTTTTATTTTGTC	79589
rs774913188	snp	G/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106728489	CTTAAAGAGTTTAGT[G/T]CAGTAAAGCACATCA	79589
rs774929040	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106782249	CAAAGAGCAAAACGA[C/T]TGTGAAAGACATCAT	79589
rs774952675	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711961	ATGAATAAGATCAGT[A/G]AGTTCATAGAATCTC	79589
rs775028949	in-del	-/A	0.0540818	0.155294	intron-variant	RNF128	GRCh38.p7	X:106707806	GCAAATGGTCCCAGG[-/A]AAAAAAAAAACACCA	79589
rs775030985	snp	A/G			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692295	CTTTATTGTGATCCT[A/G]AAAACACATCAAAAT	79589
rs775037839	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106739314	ATAGGAGTGTGCTAC[C/T]ATGTCCAGCTAATTT	79589
rs775095014	in-del	-/TGT			intron-variant	RNF128	GRCh38.p7	X:106740215	ATTTTTAGCCTCTGT[-/TGT]TGTTGTTGTTGTTGT	79589
rs775105318	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106712302	TCAATTCCCTTCTAA[A/G]GACTAATAAGCAGCA	79589
rs775111922	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106727442	CAGACCTCTGCCATG[A/G]CCAGTTTCTCTTATT	79589
rs775140304	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106779748	CACTCTTGTTTATCC[C/T]CTCATCTGTAGTTCC	79589
rs775144296	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730161	TTTTGTTTAGGAGAA[A/G]GAAACTCCACTATAT	79589
rs775145588	in-del	-/GGA			intron-variant	RNF128	GRCh38.p7	X:106770815	GAGCTGCATTCCTTT[-/GGA]GGAGAAGAGGCGCTC	79589
rs775158488	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106714064	TCCCCAGTAGTCCCA[C/G]CTACTGGGGAGGCTG	79589
rs775171044	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106784087	CTTCAATTCATATGT[A/G]TATTATATTCACTAC	79589
rs775189524	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106729630	CTACATTCAGAAAAG[C/T]ATTTTGATACTTTAA	79589
rs775234963	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772830	TTTGTCTCATTGAGA[C/G]CCATTTAAAATCATT	79589
rs775236799	snp	A/C	0.000529661	0.016265	missense	RNF128	GRCh38.p7	X:106694245	AGCTTGTGACCACAA[A/C]ACTGAGTTTAGTAAT	79589
rs775261366	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750218	TGGCACACACTACAC[A/G]TTAGGGCTTTCTCCA	79589
rs775280261	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106790372	TTTTTTCGCTATGTA[A/G]TACACCATACTTATA	79589
rs775281227	snp	C/T	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106756045	GGATGTGAAGGACCT[C/T]TTCAAGGAGAACTAC	79589
rs775308779	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749361	GCGCATTATAAGAGA[C/T]CCTTTCCAATATTTT	79589
rs775318614	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106697080	TGGCCACCCTAGCTG[G/T]CTTTGTTCTGAACTT	79589
rs775334453	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106754916	ATTAGTAGAAGAAAA[G/T]AATTAATAAAGATCA	79589
rs775388661	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752383	AGAGAAAGTAAGGGA[A/G]GAGAACAACACATTC	79589
rs775395669	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106793106	GAGGGCTTATTAAAA[C/T]GGAAAGGTCACCACC	79589
rs775417136	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106719082	GCTTAATAGGTGATT[A/G]TGATTACATACTACA	79589
rs775421025	snp	G/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106733574	TACATAGGCATAACT[G/T]TGTATTCTACTTTTG	79589
rs775455986	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106747263	AATTACCTTTGAAAC[A/G]AAGTACAGATTTAGA	79589
rs775470117	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106701577	TCTCCATAAATTAGG[C/T]ATGGAAAGAAGAAAC	79589
rs775473190	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106770626	GGACTTCTCTACACT[C/G]TTTATTCTAGTTAGC	79589
rs775473479	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784564	GGTACTACCCTCATT[G/T]TATAGATAAGTAAAC	79589
rs775485265	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106795239	AATTTTTTAAGTGCC[A/C]AGGTGATTGAAATGT	79589
rs775487922	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714920	TGATATTCCATGGTA[C/T]AGATGTACCACAGTT	79589
rs775489659	snp	C/T	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106721169	CTTCTCTCCACACAC[C/T]CACCATTTTCTTCTT	79589
rs775517485	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766971	CATTTATTAAATAGG[A/G]AATCCTTTCCCCATT	79589
rs775583186	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106717234	AGAAAGAAATTTATA[A/T]TGTATTCAATATGCA	79589
rs775585163	snp	A/G	2.83455e-05	0.00376456	intron-variant, missense	RNF128	GRCh38.p7	X:106727178	CTGGTACCGCCCGAC[A/G]GGCCCGGGGCGCTTA	79589
rs775594740	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740396	TTTACTAGTTCCACC[A/T]GGTCTGAAAGGTTCA	79589
rs775595934	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713065	TTTGTATTTTTATTA[A/G]AGATGGGATTTCACC	79589
rs775617352	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106779210	AAATTTATACCACTA[A/C]TTCTTTTTCCAGCTT	79589
rs775655008	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106709021	AGAACTTATATACAG[C/T]ATGAATTTTCTTTAT	79589
rs775673010	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735389	CTTGTCATTTCAGAC[-/A]AAATGTTGAAATAGC	79589
rs775683526	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106786520	AACAAAACGTTAAAG[-/A]AAAAATATTTTCATG	79589
rs775694588	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106737491	CTCTAAAATACTTAT[A/C]ATACCTAATACAATG	79589
rs775696520	snp	C/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106704787	AATTAGCTTCCATTT[C/G]GGAAACTAGCTAAGG	79589
rs775738541	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106781442	AATGTTGTTCAAACA[C/T]GTGTTGAATATAATC	79589
rs775785377	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106743586	TCAAATTCTACCTTG[C/T]ACATAGTATTTAAGA	79589
rs775795916	snp	C/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106776577	GGGAAAGAGAATATA[C/G]TCTAACACAACAGAA	79589
rs775823485	in-del	-/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106692722	CGTCTCCTATTTTTT[-/T]ATTTTCGGTTGTCCT	79589
rs775838364	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723339	TTTGGGAGGCCGAGG[C/T]GGGCAGATCATGAGG	79589
rs775854034	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769846	TTTCTTCCTAGCATC[A/G]ATGGTCTTTACAATT	79589
rs775914527	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787314	ATGGATGAATCTCAA[A/T]TGCATTATACTAAGT	79589
rs775955378	in-del	-/AAT	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106746586	TTTCTATACGTTGTG[-/AAT]AATAATTTTTCCCCA	79589
rs775960545	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106708138	AGAAAGATTGGGGTT[C/G]CTCGGCTTGATGACA	79589
rs775961908	snp	C/G	2.32596e-05	0.00341017	missense	RNF128	GRCh38.p7	X:106694321	TTTTCAGAAAAAATT[C/G]AAACAGCGGGCAGAA	79589
rs775964318	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770918	TTTGATGATGGTGAC[A/G]TACTGACAGGGTTTT	79589
rs775987874	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106770364	TGGTTCCATTCTCCC[C/T]GTCACTTTCAGGTAC	79589
rs775989046	in-del	-/GAA	2.4214e-05	0.00347942	intron-variant	RNF128	GRCh38.p7	X:106773198	CTATTAAAAAAAATT[-/GAA]TACTGTTCTAATTGT	79589
rs776006863	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106745324	ATTCCCTGCGATACA[C/T]CCTCCCTCCAAAAGA	79589
rs776015279	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770262	ATCTTTGTGGCATTC[C/T]CTGTACTTCCTGAAT	79589
rs776040236	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106736246	AATTGAGTTACTTGT[C/T]TTTAAAATGAGCATT	79589
rs776065029	snp	A/G	2.33419e-05	0.00341619	intron-variant	RNF128	GRCh38.p7	X:106790156	TGTTGCTACTTTACA[A/G]CTGATAATTATGTTT	79589
rs776066210	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106722581	TCCATAGAGTGGAAG[C/T]ACTTTGTTGCAGTCA	79589
rs776184943	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106767103	TACCAGTACCATGCT[-/A]TTTTGGTTACTGTAG	79589
rs776191784	snp	A/T	2.46421e-05	0.00351005	intron-variant, missense	RNF128	GRCh38.p7	X:106727215	GTAACCCGCACACGA[A/T]TTTCACGGTGCCCAC	79589
rs776216812	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726426	TTAGGCAAATGTTAG[A/G]AGGGAAAAATGTATT	79589
rs776219587	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106700747	ATTCATTTTTGCATA[C/T]ATACGTACAGAAAAC	79589
rs776248877	snp	A/T	0.000187756	0.00968725	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795725	TTAAAATCTGTGTAA[A/T]TAGAAAACTTGAACC	79589
rs776265879	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106728044	TAACGTTCTTGAAAA[A/G]GAAGAGGTTTCTGCA	79589
rs776289824	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770384	CTTTCAGGTACACCA[A/G]TCAGACGTAGATTTG	79589
rs776297794	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106749193	TAACACACTGAAAAT[C/T]GGGAGATTAAATATC	79589
rs776350375	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106709638	CGCAACCTCTGCCTC[C/T]CGGGTTCAAGAAATT	79589
rs776358671	snp	A/G	4.56538e-05	0.00477753	missense	RNF128	GRCh38.p7	X:106694154	TAGAGACATGTGAAT[A/G]TGGCGTTTATGGATT	79589
rs776359413	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713132	GTCGTCCCCCACCCC[C/T]CGCCTTGGGCACCCA	79589
rs776402093	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740185	TGATAGTGTTTTTTC[C/T]TTCCAGGGACCTCAC	79589
rs776420423	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106766248	TAATGGGATGGCTAG[A/G]TCAAATGGTATTTCT	79589
rs776421074	in-del	-/GT/GTGT			intron-variant	RNF128	GRCh38.p7	X:106779348	TCCCTACACAGTTAC[-/GT/GTGT]GTGTGTGTGTGTGTG	79589
rs776434222	snp	A/G	2.2799e-05	0.00337624	synonymous-codon	RNF128	GRCh38.p7	X:106772992	TCAAAGAGGCATACA[A/G]GTGACAATGGTCATA	79589
rs776446177	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106739475	TCATATTTTAACTGT[A/G]TCAAAGCTTTGTCAA	79589
rs776461523	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106718975	AATGCATATAGTTGG[A/C]AGCTGTGAATTTGTG	79589
rs776483746	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792655	CCCAAGAAGTTAGGG[A/G]AGCCCAGTATAACTC	79589
rs776501986	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106788122	TTATTTTTTAACTTA[C/T]CTTCATTTAAATATA	79589
rs776515358	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106703745	GAAGGGTCATCAACA[C/T]AGAAGGTGATAGCAG	79589
rs776517274	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751272	AAAATCTGTGTGTTT[A/G]GGGGAAGGAGAGCAC	79589
rs776532385	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106742555	TCATCGATCCAGCAC[A/G]ATGGTTCTGAAATTA	79589
rs776553280	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106735103	CATGCACCATAGCAC[A/G]TAGTTACTGCTTGAA	79589
rs776580730	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750265	TCTAAACATTTACTA[C/G]TGCACCCATGAATGT	79589
rs776602417	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728658	TGAGTGGCTGGATGG[C/T]GTAATGGAAAGAACA	79589
rs776606670	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106716771	CTGTCTCTAATGAAG[A/G]AGATAGGCATGTAAG	79589
rs776685175	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106775202	ATTTGTATATTGTGC[A/G]GTTTTTTATCTGCGA	79589
rs776690113	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106707088	TTTGCCTATTTTTAT[G/T]TATTCTTATGTATTC	79589
rs776693863	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106732997	CCAACTGAGGAGGAA[C/T]AATATTTGGGGGAAA	79589
rs776706482	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760637	TGGCAATTCAATTAC[C/T]GGGTATCTATCCAAA	79589
rs776712889	in-del	-/A	0.01368	0.0815649	intron-variant	RNF128	GRCh38.p7	X:106704272	AACCCCGTCTCTACT[-/A]AAAAATACAAAAAAG	79589
rs776743767	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106698999	GCCTTCCTCATCCTC[A/G]CTCCCACATCTCATT	79589
rs776753071	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106706716	TACTACTTTAAACGG[C/T]GAAAGATGTATAGGA	79589
rs776769059	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778914	TACACGAAATTATCT[A/G]GAAGATTCATTAAGT	79589
rs776783530	snp	A/G	3.36225e-05	0.00410001	intron-variant, missense	RNF128	GRCh38.p7	X:106726969	GCTGCGGCTTTTCCA[A/G]ATTGCTGGCATGGTG	79589
rs776816766	in-del	-/AC			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693363	GCCTGCTAAGAAAAC[-/AC]ACACACACACACACA	79589
rs776825867	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106706033	AGGGCAGCTTAAAGG[C/T]TTAAAGAAGGCCTAC	79589
rs776837790	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106785986	TTGCTGTTGTTAAGA[C/T]GTCGGTTCCCCACCA	79589
rs776841169	snp	C/T	3.89219e-05	0.00441128	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726896	AGGGGCGCTAGGGAA[C/T]TGCGGAGCGCGCGCG	79589
rs776851509	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106758258	GAAAACTGTAAAACA[A/T]TGATATAAGAAATTG	79589
rs776856092	snp	A/C	0.00105736	0.0229687	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693986	CATCTTAAATTTTAT[A/C]CTCAAATGAATGAGC	79589
rs776873021	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106776719	TCAAATTTATGGAAT[A/T]TTTTTTTGTAAAATT	79589
rs776911695	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106724464	CGTTTTTGGATAAAG[A/T]CTAAACTCCCTAGCT	79589
rs776948858	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106790386	AATACACCATACTTA[C/T]AGTTTATACCTAAAA	79589
rs776963528	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106772152	TGTACTTTATTTTTT[-/T]CCACAAAACTTATAT	79589
rs777023046	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106710529	TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG	79589
rs777023398	in-del	-/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106715023	TGAAAATTTGTGAAT[-/G]GCTTTCTGTGAATGT	79589
rs777039019	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106763879	AGGACTGAAGCACAG[A/C]ATTGTTGCTAAGATG	79589
rs777110638	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106714810	TCATTGTATGTAAAC[-/T]TTTTTGGGATTGGCT	79589
rs777115258	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106697507	TTTCTCACTGAAAAT[A/C]TACTTCACCCACCCT	79589
rs777117445	snp	A/G	0.000182932	0.00956205	missense	RNF128	GRCh38.p7	X:106694094	TTTCAATGAGTGCCT[A/G]TGTGACTGTGACTTA	79589
rs777119379	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752514	CCCCCTAATGCATAT[A/G]TGGCTAAAGTGACCA	79589
rs777128457	snp	A/G	2.34549e-05	0.00342446	intron-variant	RNF128	GRCh38.p7	X:106790145	ATTAGGTAAAGTGTT[A/G]CTACTTTACAACTGA	79589
rs777137224	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787406	AGCCAAAACTATAAA[A/T]ACAGATCAGTGGTTG	79589
rs777137269	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	RNF128	GRCh38.p7	X:106692635	TCCACTCCAACACTG[A/G]TATTTCAGATGTTTA	79589
rs777175326	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106739799	TACTCAGGTACTAGA[A/G]TGTTCTTTTTTATAG	79589
rs777176148	snp	C/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106764406	GTGCAGTGGCTGACG[C/T]CTCTAATCCCTGCAC	79589
rs777187489	snp	C/T	7.49756e-05	0.00612227	intron-variant	RNF128	GRCh38.p7	X:106787881	TTTAATGTATTTTTT[C/T]TTATCTGTCAGAGTA	79589
rs777212957	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106761282	GTCAAAAAATAACAG[A/G]TGTTAACAAGGTTTT	79589
rs777215080	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106769276	GATATCCTTGTTAAC[G/T]TACTGTCTCGTTGAT	79589
rs777246285	snp	A/G	2.7715e-05	0.00372247	intron-variant	RNF128	GRCh38.p7	X:106788022	TTGATTTTCTTCTAT[A/G]TCTTCAATAAAATAG	79589
rs777257225	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725337	TTGTTTGGTATATGA[C/T]GTTAATTTTCCTCTA	79589
rs777258392	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106749070	GATGATATTTTAATC[C/T]ATCTTTGAAAAAAAT	79589
rs777268562	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768501	TTCTAGTTTATTTGC[G/T]TAGAGGGGTTTATAG	79589
rs777279629	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106722407	TTGGTCTGGGTGGAA[A/C]CTGTGATTCTGCATT	79589
rs777311545	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106700395	GAAGACAGAGACCAC[A/G]TCTGTCATGTTTGCC	79589
rs777312458	snp	G/T	0.000357058	0.0133567	intron-variant	RNF128	GRCh38.p7	X:106785050	TTCTAATACCTGCTG[G/T]TTTTTTTTTTACAGA	79589
rs777344389	snp	C/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106697823	CTTCTAACTCAGTTT[C/G]CCATTGTGCTGTGTC	79589
rs777351737	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794646	CTTATTGCTACCGGG[G/T]TGTCATTGCTATTGG	79589
rs777370635	snp	A/T	0.00819179	0.0634727	intron-variant	RNF128	GRCh38.p7	X:106762317	CATTCTCCACTTTTG[A/T]TTTTTTTTTTTTTTT	79589
rs777371089	snp	A/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725604	TATTTTAGAATTGTG[A/T]CTCTGAACCTGTTTA	79589
rs777411423	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732724	GATTAGCCTGGTTTT[A/G]TGGATTTTTAATGGC	79589
rs777440199	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764998	TCCAGATCCATAAGG[C/G]ATATTTGGGTCATAT	79589
rs777466553	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106778671	GCACCTAGTAAGCAG[A/T]CCCTTCATCTGAGTC	79589
rs777488290	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106743327	GGATCAATGGTGATA[A/T]TAACAACTGACTTTT	79589
rs777506485	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106784402	TCCATAAATGAGCCT[A/G]TGGCTTGCTTTTGCA	79589
rs777517964	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106755498	GTCTCTCTGATGAAC[A/G]TCAATGCAAAACCTC	79589
rs777531288	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106715360	CCTCTTTGGTGAAAT[A/G]TTTATTCATGTCTTT	79589
rs777531354	snp	C/T	0.000529661	0.016265	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726639	CTCCCTCCCAGCCAC[C/T]TCTACCCCCAGTCGG	79589
rs777533056	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106718694	TGATTTGTGGTGAAG[C/T]CAAAACCGAAGTCAT	79589
rs777562783	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106708130	ATAACACCAGAAAGA[C/T]TGGGGTTCCTCGGCT	79589
rs777580711	snp	C/T	0.00105904	0.0229869	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725064	GTACAATATAGTTGG[C/T]TGTCATTCAGGTAAT	79589
rs777609563	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106776425	GGATTTACTAACTAA[A/C]ATAGACAGATTAGAA	79589
rs777631807	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106780844	TACCAGCTGTCTGGA[A/C]TTTAGTCAAGCTTCT	79589
rs777688885	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716208	GTCAGAGGCAAACAT[G/T]CCTGCCTCTATTCTA	79589
rs777721179	snp	A/C	0.00581083	0.0535878	intron-variant	RNF128	GRCh38.p7	X:106752265	ATGCTGGTTTCTGGT[A/C]TAATGCAGCTCAGTC	79589
rs777728010	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106755728	ACGATTAAAAACCCT[-/A]AAAAAGGGCAATTAG	79589
rs777751375	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106777249	ATGAAGAAGAAGTAG[A/G]ATGATTTAGTTCATT	79589
rs777767610	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106760959	TTTTGCATAGCAAAA[G/T]AAACTATCAACAGAG	79589
rs777816844	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106787844	TGGTTAAGTACATGT[A/C]TGTTCTGATCTTGTT	79589
rs777826820	snp	A/G	2.28671e-05	0.00338127	synonymous-codon	RNF128	GRCh38.p7	X:106694281	GAAGCCCTGGATTGC[A/G]CTGATAGAAAGAGGT	79589
rs777828109	snp	C/G	9.3124e-05	0.006823	missense	RNF128	GRCh38.p7	X:106791216	GAACCGCCTCTGGAG[C/G]AACACGTGCAGTCAA	79589
rs777856226	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106734882	ACTGCACTGGGGTTA[C/T]TTTATGGTGGTGATC	79589
rs777866580	snp	C/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106790933	GAGACTTGTGATCAT[C/G]AAAAGGGATCATAGG	79589
rs777867546	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758135	TATTTCTAGATGCCA[A/G]TGGCACACAATCTGA	79589
rs777952973	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106746147	ATGTTTGGACAGTAT[A/T]GAATGTAGTTTTATA	79589
rs777953095	snp	A/C	0.00475684	0.0485365	intron-variant	RNF128	GRCh38.p7	X:106734463	ACAATTGAGGTTTGC[A/C]CCTGGTTTCCCTGTT	79589
rs777984996	in-del	-/A	0.00581083	0.0535878	intron-variant	RNF128	GRCh38.p7	X:106718508	ACAGAGACAGCTTAG[-/A]AAAAAATGTACCTCC	79589
rs777995303	snp	C/T	0.0068637	0.0581785	intron-variant	RNF128	GRCh38.p7	X:106699220	AATGTAATTCCACCC[C/T]AGTTAGAATAAAATC	79589
rs778038667	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106698209	TTTGGAAGTTAAATA[C/T]GTTATTTTTAGGTAA	79589
rs778041011	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106717631	AATGAATAGAGCAGA[C/T]GAATTTTATTTTAAA	79589
rs778059271	in-del	-/TTTAA	7.20833e-05	0.00600304	intron-variant	RNF128	GRCh38.p7	X:106791040	GTACACTGAGAGGCT[-/TTTAA]TTTGTTACATGTTCT	79589
rs778065330	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106766238	ATATGCCCAGTAATG[G/T]GATGGCTAGATCAAA	79589
rs778077810	in-del	-/G	0.000261826	0.0114387	intron-variant, frameshift-variant	RNF128	GRCh38.p7	X:106727022	AGGCACCCGGTTCCC[-/G]GGGGGGCTGAAGCAG	79589
rs778080481	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702929	ATTCAACAGTATAGT[A/G]ATGTTAATAGTCATG	79589
rs778083396	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106724067	CCTCAAAATCGACAT[A/C]TCTAAAGTGAACTCA	79589
rs778118536	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106742655	TACTTACACATTGTT[C/T]GCCTTATTCACTGTG	79589
rs778138133	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106766119	CCAGTCTATTATTGA[A/T]GGACATTTGGGTTGG	79589
rs778159883	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106712808	ACTTTTAGCCAGTTG[C/T]TTTGGTGTTATGTAA	79589
rs778166120	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106729421	GATTATATATATATA[C/T]ACTACCCAGCTGATA	79589
rs778166905	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106787259	GTATACTATTTAGCA[A/G]TAAAAGTGTGATGGG	79589
rs778171638	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106745472	GTTCATTTGTGTGGC[C/T]ATAAAGAAATACGTG	79589
rs778182371	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790074	TAGTGTGTTTAAAAG[G/T]AAAGGCATCCATTCA	79589
rs778211076	snp	A/G	3.32276e-05	0.00407586	intron-variant, missense	RNF128	GRCh38.p7	X:106727131	AGGGCGTGTACGGCC[A/G]GGACTCGCCGCTGGA	79589
rs778217481	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106713902	ATAGCAAGGCCGGGC[A/G]CGGTGGCTCACGCCT	79589
rs778219393	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106731884	CCTCTTGATTGGTCT[C/T]CTTGCCTCCAGTAGT	79589
rs778250585	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763446	ACAGATATTTTCAAG[C/T]GCATGGGAAGTATCA	79589
rs778257215	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106752353	CAGCATGGTGAGAGA[A/G]ATTCCTTTTGTTTGA	79589
rs778268208	snp	A/G	0.000465766	0.0152534	intron-variant, missense	RNF128	GRCh38.p7	X:106726948	CCGGGGTCTCCTGCC[A/G]CGGTGGCTGCGGCTT	79589
rs778310805	snp	A/G	2.31715e-05	0.0034037	synonymous-codon	RNF128	GRCh38.p7	X:106785109	TATTGGAAGGCTTCA[A/G]CTACGCACACTGAAA	79589
rs778358350	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750169	CAATTCCACATTCAC[A/G]TGGCTATGGTGGGAG	79589
rs778392227	in-del	-/CCCC/CCCT	0.00158842	0.0281444	intron-variant	RNF128	GRCh38.p7	X:106765860	ATCTCCTAATGCTAT[-/CCCC/CCCT]CCCCCCCAGCCCCCC	79589
rs778392960	snp	C/T	0.000310756	0.0124612	intron-variant	RNF128	GRCh38.p7	X:106785179	TATTTTAAAGCAGTG[C/T]TACCAAGCCATTGTT	79589
rs778430380	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106713534	AAAGCAAATCTTATT[C/G]TGAATGTTCTAGAGA	79589
rs778435294	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106764996	TCTCCAGATCCATAA[A/G]GGATATTTGGGTCAT	79589
rs778447764	in-del	-/T			intron-variant	RNF128	GRCh38.p7	X:106754411	AATGTTTTCTTTCTC[-/T]TTTTTTTTTTTTTTT	79589
rs778449792	snp	A/C	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106728276	AGAGACACGTGTAAT[A/C]GCAGTGTATCATAGT	79589
rs778456484	in-del	-/TC			intron-variant	RNF128	GRCh38.p7	X:106697488	ATCAGGGGCAACTTG[-/TC]TCTTTCTCACTGAAA	79589
rs778468912	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106787685	AAATCAGTGCTACAT[C/G]TTTCCCTTTGTTCTG	79589
rs778511428	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106739251	TTCAACCTCTACATC[C/T]CGGGTTCAAGCGATT	79589
rs778517667	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106750782	GCTAGAAGCAACAAC[A/T]GAAGTGAGAACCTTC	79589
rs778556410	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106791405	CCTTAATATACATAT[A/G]TTCAAATGTATTTGA	79589
rs778575877	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714419	AAAATGTAGATTTAC[A/C]TGCAGTTGTAAGAAA	79589
rs778626824	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106742468	ACATACTGAATGAAG[C/G]AATGGGGCCCAGAGA	79589
rs778627441	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106755265	AAGAAAGCCATGACA[A/G]ATAGTCCCCCAGTAA	79589
rs778669633	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106776497	CTTGCAAAGGTCATA[A/T]AGCTTTGATAAACTG	79589
rs778678918	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106734844	GTAGGAGCCCAGTCA[A/C]CCACAGAAATATTCT	79589
rs778736144	snp	A/G					GRCh38.p7	X:106736587	ACCTTGAAGGTGTCC[A/G]TAACTTACTCCCATA	79589
rs778763356	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106768663	GATCTTTTCAAAAAA[C/T]CAGCTCCTGGATTCA	79589
rs778785751	snp	C/T	2.36105e-05	0.0034358	synonymous-codon	RNF128	GRCh38.p7	X:106694053	CCTTGTAATTTTTAC[C/T]TTTTTACTTAAAATT	79589
rs778791462	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106705573	TCAATTCAGCAGAGG[A/C]AGAGAAGTGTACAAT	79589
rs778836497	snp	G/T	2.65954e-05	0.0036465	intron-variant	RNF128	GRCh38.p7	X:106788009	CGTGCAAGTAAGTTT[G/T]ATTTTCTTCTATATC	79589
rs778842720	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106706508	AAACTTCAAGCATGC[A/G]TGGCTTCTACCAGAA	79589
rs778848006	snp	A/G	0.0026455	0.0362733	intron-variant	RNF128	GRCh38.p7	X:106697966	TTCATATTCTAGCTT[A/G]CCAGAAGGAATAATG	79589
rs778904532	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106719388	ACCACACTCAGCTAA[C/T]TTTTGTACTTTTAGT	79589
rs778919147	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106778544	CTGGAAAAATGGACC[A/G]TGTTGTACCAGCCTG	79589
rs778931114	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106763503	TGATTAGGAAGCCAA[C/T]TCAGGGTTTTTTGTT	79589
rs778931458	snp	C/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106744680	TAACCAGGATGGTCT[C/G]TATCTCCTGACCTCG	79589
rs779003532	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106752803	GGAAGCTCAGTGAAA[C/T]TCCAGATAACACAGA	79589
rs779015907	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106733526	CTACAACACAGATGA[C/T]ACCATTAATATTCCT	79589
rs779042644	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106778292	ACTATACTGACTACT[A/G]TACCAACTGAAGTGA	79589
rs779128407	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106710237	CCACTAGAATTTGTT[C/T]TGAACAGAAGGAAAG	79589
rs779188066	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106764205	CTCCTGACCTCGTGA[C/T]CCACCCACCTCAGCC	79589
rs779198358	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106741325	CATCCAAGCCATCAG[C/T]CTACTAGTGAACCAG	79589
rs779240710	snp	C/T	4.57169e-05	0.00478083	synonymous-codon	RNF128	GRCh38.p7	X:106773118	TTTTATCTTTTATTC[C/T]GCTCGAAGGCTACGG	79589
rs779243567	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770712	CTCCTTTAGTTCAGA[A/G]AAGTTTGTTATTACC	79589
rs779247842	in-del	-/GTTTTTT	0.00802943	0.062851	frameshift-variant	RNF128	GRCh38.p7	X:106694025	AGGAGAATAGGTCCA[-/GTTTTTT]TTGGCTCCTTGTAAT	79589
rs779275484	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106695671	TTCCTGTGTTTTTAC[A/G]AGTGACTTTCATTTT	79589
rs779275828	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106730055	CACTCACTCTCATAG[C/G]GGCCTGCACTTGAAT	79589
rs779293673	snp	A/C	2.29166e-05	0.00338493	synonymous-codon	RNF128	GRCh38.p7	X:106791110	ACAAGTCCCTGTATC[A/C]AATGAAATATCTAAT	79589
rs779300758	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106704382	AGCTTGCAGTGAGCT[A/G]AGATCGCGCCACGCA	79589
rs779313532	snp	A/G	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106740030	CAACCCAATCCCCAT[A/G]TTAAAAACTATACCT	79589
rs779315257	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106748374	GCAAAACTCAGCAAC[A/G]TAAACAACATAGATT	79589
rs779318068	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731042	GGCATAATAATAAAC[-/T]TGCCTCCTAAGGTTG	79589
rs779319823	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106729191	CTTGGCTCCCACTAT[A/T]TGCCAGGCACTCTAC	79589
rs779327713	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106791690	GGAAACTGTTTAAGA[A/T]TGGTATGTGCTGCCA	79589
rs779331767	in-del	-/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106781336	GTTCTTGAAATTCTG[-/T]TTTTTTAAGGAGTAA	79589
rs779341406	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774513	ATTGCTCCCATTTTC[A/T]AAAGATTTTCTCTTG	79589
rs779350973	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106702816	AGAACAGTGGAAGAG[C/T]GAATTCCAGGAGATG	79589
rs779365047	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106752024	TGCAATTTGGGTACC[A/G]GTTCAGCCACAGTAA	79589
rs779373747	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766622	GATATTAGCCCTTTG[C/T]CAGATGGGTAAATTG	79589
rs779411570	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106694817	AAACTGCAAAACAGT[C/T]TCATTATGCTTAAAT	79589
rs779421689	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106766164	TATTGTGAATAGTGC[A/C]GAAATAAACATACGT	79589
rs779428165	snp	A/C/G/T	6.95499e-05	0.00589672	synonymous-codon	RNF128	GRCh38.p7	X:106791206	GGGAACAGATGAACC[A/C/G/T]CCTCTGGAGGAACAC	79589
rs779451058	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106727817	CAGATTTTCCCCTCC[C/T]CTCCCTGTTTTTCTC	79589
rs779457844	snp	A/G	2.32418e-05	0.00340886	synonymous-codon	RNF128	GRCh38.p7	X:106791086	TGTTGAAGATGGATC[A/G]GTGTCTTTACAAGTC	79589
rs779490175	snp	A/G	0.00317376	0.039709	intron-variant	RNF128	GRCh38.p7	X:106764120	GGTGCCCGCCACCAC[A/G]CCCGACTAATTTTTT	79589
rs779505813	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106718750	GTTGAAGGCCTGCTT[C/G]TTCCTTGCCTGTTTC	79589
rs779510750	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106694889	ACTTGACTCTACTGT[A/G]TGCTTGTAAGATTTG	79589
rs779534348	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106758242	AAGAGAGCTCTACAA[C/T]GAAAACTGTAAAACA	79589
rs779551470	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106752447	ACCCAAGACCACCAA[A/C]ACAGTACCTCTACTA	79589
rs779581267	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106783769	CTTGGCGCCAACCTC[C/T]GCTTCTGGTGAAAGC	79589
rs779608546	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106732196	GCAACACAAATGCCT[C/T]CTCATCTTTGAAGCC	79589
rs779623191	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106774733	TTCTCAGTATAACAG[A/C]GGAATGGTGTGCCAC	79589
rs779659617	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723690	ATATCCCAACCATAC[C/G]GAACTACTGAATGCT	79589
rs779674011	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106751079	AGGAACACCAAATTG[A/G]ACAACTCCCCACACA	79589
rs779684192	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106750953	GTTAAATAATGGCAT[A/C]CAAAGATAATCCACT	79589
rs779700237	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714507	TAACGATAGTACAAT[A/C]TCACAACCAGGAAAT	79589
rs779703598	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106740897	TATATCTTGTTAGTC[A/G]TAGTTGTTTCACCTT	79589
rs779755817	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106775923	CTGTAACCATAAATT[A/C]TGATGACTGAATGCT	79589
rs779762567	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106718057	CTGACACATGTTAGC[C/T]TGCTTACTGGAATGT	79589
rs779772952	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106764606	CAGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATT	79589
rs779778114	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106776236	ACATTTTCGGGTACC[A/G]TAAATGTATCCTAAC	79589
rs779825874	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106720464	AGCAACTCTCCTGCC[A/T]CAGCCTCTCAAAATG	79589
rs779881123	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106723145	AAATACTGTATAAGA[A/G]AAGTAGGAAAAAAAG	79589
rs779888040	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106754645	ACAGAAACTTTGGAA[A/G]CTATACAAATACATG	79589
rs779891340	in-del	-/AGA	2.3467e-05	0.00342534	cds-indel	RNF128	GRCh38.p7	X:106694333	ATTCAAACAGCGGGC[-/AGA]AGAAATGCTGATGCT	79589
rs779908432	snp	C/T	2.55376e-05	0.00357325	intron-variant	RNF128	GRCh38.p7	X:106694420	TTTGGTAAGTAATAA[C/T]TGATTCACAAAGAGA	79589
rs779929012	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106695319	TATTGCCAAATTTGG[C/T]CTCTAAGAAAATTAA	79589
rs779949635	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106770074	GTTGAATATTGGCCC[C/T]GACTCTCTTCTGATT	79589
rs779968781	snp	A/G	6.86986e-05	0.00586043	missense	RNF128	GRCh38.p7	X:106772942	GTTGCAATCATGATC[A/G]GCAATCTGAAAGGCA	79589
rs779989843	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106721610	TTCAAAAAGGCTCCT[G/T]GCCCATATATATCCT	79589
rs780002635	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106780584	CGTTTGACATCATAT[A/G]CTTGCTTTTTAAAAT	79589
rs780002928	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106769538	ACTAGGATTGCTACA[C/T]CTGCTTTGTTTTTTT	79589
rs780011566	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106763529	TTGTTTTCGTTGAGA[C/T]GGAGTCTCGCTCTGT	79589
rs780034741	in-del	-/A	0.00528398	0.051128	intron-variant	RNF128	GRCh38.p7	X:106793334	GAGCAACTGTGATTT[-/A]ACATGAGGTGCAGGG	79589
rs780061306	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772404	TAGTTTGTACATTTG[G/T]GTTTGTAAACATTGT	79589
rs780062733	in-del	-/A	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106735898	TCACTAGCTTTTTTT[-/A]ACCCTCCCCCCAACA	79589
rs780063521	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106765086	CCATTGTTTTTGAGA[C/T]TTTCCTTTTGTAAAT	79589
rs780070019	snp	A/G			downstream-variant-500B	RNF128	GRCh38.p7	X:106797375	CCCCCACCAGGCCTC[A/G]CCCCCGACATTGAGA	79589
rs780112210	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106771723	AGGCGATGGCCTGCC[C/T]TGCTCCGTGGGCTGT	79589
rs780154499	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106774237	ATTTTATTTTACTGA[C/G]AAAATTGAAGCAATC	79589
rs780216388	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106698612	TGAGCCTCAAATCTG[A/T]CTAATTCTGTGCATC	79589
rs780248296	in-del	-/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106701770	TTATTAAAAACAAGA[-/T]GAAGTACCATGGTGA	79589
rs780263589	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106783627	CTTGCCATGCTGCAC[A/T]TGCTACCATTATATT	79589
rs780280332	snp	C/G	2.30168e-05	0.00339233	intron-variant, synonymous-codon	RNF128	GRCh38.p7	X:106727360	CATCTTTAACTTCCC[C/G]GGGACCCGCAATGAG	79589
rs780290319	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106728897	TTAAAGGAGAAACTG[C/T]ATCTCTCTTGGCCGA	79589
rs780329238	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106762844	CATGGACACAAAGAA[A/G]GGAACAACGGACACC	79589
rs780340165	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732497	GGGTCACAAGATTCA[C/G]TAGAAAAGTATCTAG	79589
rs780343435	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702581	TCTTCCTTCATTCGA[A/G]GAGTACATTCCCTAG	79589
rs780348754	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106748690	GACAAATGTCACATG[A/T]TCTCACTCATGTGGG	79589
rs780353543	snp	C/G	0.00211696	0.0324653	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726751	CATCTGCGGCAACCT[C/G]TGTGCTGACGCTACG	79589
rs780356868	snp	A/T	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106788198	TTGGTATAAGTCTAA[A/T]TGTAATCTGCTTCAA	79589
rs780406769	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106718155	TATGCCCTAAACACC[A/G]TATAGAGGCCAAACA	79589
rs780412597	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106783325	ATTTGCTACAAATAT[C/T]TGTAGCATTTGTAGC	79589
rs780420032	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106711418	CATTTATTTGGATCT[C/T]GACGGTTTTTTAAAT	79589
rs780444893	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106712842	AGCCTGACTCTTGAC[C/T]ACCTCCTAATATTCT	79589
rs780459528	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106748035	GTCTTCTGTATAACC[A/G]GTCCACAAGAAAGTT	79589
rs780461983	in-del	-/AG	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106696033	TATGTGACTCTGAAC[-/AG]AGTTTTAAAAAGGAG	79589
rs780464872	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106731285	AGACTGAATTTTAAC[A/G]GGAAAAAGATCTTTT	79589
rs780466548	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106769353	TGTGCGTGTCTAAGT[A/C]TCTTTGTAGGTCTCT	79589
rs780471403	snp	A/G			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693472	TTCTACTAATGCCAT[A/G]GCAATTAAACTCATG	79589
rs780484612	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106767230	ATGAACTTTAAAGTA[A/G]TTTTTTCCAATTCTA	79589
rs780498675	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106792078	GATACCACTTCTGAA[A/G]ATATCACAATGAATA	79589
rs780526543	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106759653	ACATATGGAACTGGA[C/G]AATTATTATGTTAAG	79589
rs780533936	in-del	-/TTAG	1.64749e-05	0.00287005	utr-variant-3-prime	RNF128	GRCh38.p7	X:106795735	GTAAATAGAAAACTT[-/TTAG]GAACCATTAGTAATA	79589
rs780581836	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106758522	GAAACATATTACCTG[A/T]CTTTAAATTATACTA	79589
rs780592673	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106746085	TAGATCTTGTTCATT[C/G]TGGATATCAGCAAAT	79589
rs780605315	snp	A/G/T			intron-variant	RNF128	GRCh38.p7	X:106699817	TGAAGCTTTTCCTGC[A/G/T]TGGGACACTTTTTAC	79589
rs780634322	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106767342	TGATTCTTCCTATCC[A/G]TGAACACGGAATGTT	79589
rs780643843	snp	A/G			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106726139	AGAGGCATCTGATGC[A/G]GTACATGAAACCTAG	79589
rs780658001	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106773938	TTCCCGTGGCCCTTC[A/T]TTCTCTTTGTTATAG	79589
rs780668011	snp	A/G	4.58574e-05	0.00478817	missense	RNF128	GRCh38.p7	X:106694297	CTGATAGAAAGAGGT[A/G]ATTGTACATTTTCAG	79589
rs780686915	snp	A/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106731414	TACTACTTAATCACC[A/T]CCCAATCCCTTCTCA	79589
rs780702817	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106760004	CATTTACCCTGATGT[A/G]ATTATTACAGATTGT	79589
rs780707116	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106721422	ACATCTCTATAGAGT[C/T]GGTGTGATGGGAAAC	79589
rs780710958	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106750563	GAAATCCAGTGCATA[A/G]CCAGGATTCAGGAAA	79589
rs780733602	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106732544	TCATCGAGCATTTAT[A/C]AAAGGTCTGCTGTCT	79589
rs780790438	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106711191	CCCCACCTACTCACC[A/G]CCTAGCCCCATGGGA	79589
rs780792920	snp	A/C	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106723957	CTTTTGTCTCTCTAC[A/C]CCCCTGTCTCTCCCA	79589
rs780793147	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106771828	GCATCACTCACACTG[A/G]GAGCTACAGACTGGA	79589
rs780815498	in-del	-/ATAA	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106741024	ATTCCTCTAGAAAAC[-/ATAA]ATAAATAGCAACTGC	79589
rs780828905	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106794642	CATGCTTATTGCTAC[C/T]GGGGTGTCATTGCTA	79589
rs780846063	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106699952	ATTTTCTATCAAAAC[C/T]TTCAGGTCGTTCTTG	79589
rs780904581	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752971	ATCAAGCAGAAGAAA[A/C]AAGTATTGAGCTTGA	79589
rs780918837	snp	G/T			downstream-variant-500B	RNF128	GRCh38.p7	X:106797098	AAAACAGGATTAATT[G/T]GCTCATGGTTTTATA	79589
rs780947727	snp	A/G	2.36186e-05	0.00343639	missense	RNF128	GRCh38.p7	X:106791066	ACATGTTCTTTAAAG[A/G]TGGATGTTGAAGATG	79589
rs780976424	snp	C/T			upstream-variant-2KB	RNF128	GRCh38.p7	X:106693259	CTGCCATGGGCAAGG[C/T]ACTATACTTGAAAGG	79589
rs780990660	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106703307	CCCTTTATGAAGGCA[A/G]TTGTTAATTGTAAGT	79589
rs781004506	snp	A/T			intron-variant	RNF128	GRCh38.p7	X:106783420	AACATTTTATTGAGT[A/T]TCTGCTATATGCCAG	79589
rs781004715	snp	A/G	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106706325	AAACAATGTGGATTT[A/G]TTTATACACATTTTA	79589
rs781023492	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106714669	TCCATTGCAACAGAG[C/T]TCCTTCGTATTGTCC	79589
rs781036853	snp	C/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106735914	ACCCTCCCCCCAACA[C/T]ACACACACATAAAAA	79589
rs781043569	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106705078	AGGGATGGAGAAGCA[C/T]GTCAATGTTTGGGCA	79589
rs781078979	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106716372	ACATGTATATGACAA[C/T]CCAGAAAAGGCAAAA	79589
rs781084480	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106764151	TTTGTATTTTTAGAA[A/G]AGACGGGGTTTCACC	79589
rs781126067	snp	C/G	0.116753	0.211531	upstream-variant-2KB	RNF128	GRCh38.p7	X:106693391	ACACACACACACACA[C/G]ACACACACAGAGAGA	79589
rs781137435	snp	C/T	0.00158814	0.0281345	intron-variant	RNF128	GRCh38.p7	X:106763696	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	79589
rs781138449	snp	A/G	2.27988e-05	0.00337622	missense	RNF128	GRCh38.p7	X:106772991	TTCAAAGAGGCATAC[A/G]AGTGACAATGGTCAT	79589
rs781160215	snp	C/T	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106788380	AATATATATTATATA[C/T]TATATATAATATATA	79589
rs781207335	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106699528	TACTGCAAATAGCCT[C/T]CAAACTGGGCTCCCT	79589
rs781209313	snp	A/T	0.00105904	0.0229869	intron-variant	RNF128	GRCh38.p7	X:106754556	TGAGCCAGCATGCCC[A/T]GCCAAAATTTTTTTT	79589
rs781217437	snp	G/T	0.000923876	0.0214729	intron-variant, missense	RNF128	GRCh38.p7	X:106727161	AGCCTGTGGCTGGGG[G/T]CCTGGTACCGCCCGA	79589
rs781222964	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106738629	TAACAATGGAAATGG[C/T]TATGACCCTTTTGCT	79589
rs781223135	snp	A/G	0.00105904	0.0229869	intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106724975	AATGGAAAAACATTA[A/G]TAAATGTCTCTCTGA	79589
rs781242378	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106752143	ACACCACCACCCTGA[A/G]GGGAAAGACACAAGC	79589
rs781263401	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106790813	ATTATTTTATGAAGT[A/G]CTGGTATCACCCAAA	79589
rs781282314	snp	A/C	0.00370173	0.0428621	intron-variant	RNF128	GRCh38.p7	X:106766092	GGTATATATGTGCCA[A/C]ATTTTCTTAATCCAG	79589
rs781290648	in-del	-/A	4.76485e-05	0.00488078	intron-variant	RNF128	GRCh38.p7	X:106795540	GTCTTAAAAGAGGAG[-/A]GGGGCAAAATCATCC	79589
rs781362696	snp	A/C	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106728141	TGGTATGAGGTTACT[A/C]TTTTTCCCCGTCGGT	79589
rs781422363	snp	A/G	0.000114181	0.00755497	missense	RNF128	GRCh38.p7	X:106795669	ACCTTTGAAGAAGAC[A/G]AAACTCCTAATCAAG	79589
rs781427142	in-del	-/TCT			intron-variant	RNF128	GRCh38.p7	X:106769433	TTTAGGATAGTCAGC[-/TCT]TCTTGTTGAATTGAT	79589
rs781453184	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106743645	TATCAAAGGATAATA[A/T]CTACAGTTATCTGAA	79589
rs781481233	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106745949	AGAGTTTGGGATATA[A/G]GAGGAAAAGCCAAGC	79589
rs781481841	snp	C/T			intron-variant	RNF128	GRCh38.p7	X:106715514	GGCTATCTGCTAAGA[C/T]AGATGCCCTAACATT	79589
rs781489345	snp	C/T	0.00091659	0.0213882	intron-variant, utr-variant-5-prime	RNF128	GRCh38.p7	X:106726899	GGCGCTAGGGAACTG[C/T]GGAGCGCGCGCGCCA	79589
rs781492897	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106702846	GATGTTTCAGAGTGT[C/T]CCTCATCACATCATG	79589
rs781502035	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106708594	TAAGTGCTTTCAGAG[A/G]AAGAAACTCTTTTAA	79589
rs781512100	snp	A/G	0.0105399	0.0718252	intron-variant	RNF128	GRCh38.p7	X:106717456	TATTGCTGATAATCT[A/G]GATATGTGAAAGTAA	79589
rs781526670	snp	A/G	0.000529661	0.016265	utr-variant-5-prime	RNF128	GRCh38.p7	X:106693929	CTGTTCAGCAGGGAC[A/G]TGAGTGGACAATGGT	79589
rs781527320	snp	A/G	0.00211696	0.0324653	intron-variant	RNF128	GRCh38.p7	X:106749880	ACTGCACTCCAGCCT[A/G]GGCAACAGAGCGAGA	79589
rs781536294	snp	C/T			intron-variant, upstream-variant-2KB	RNF128	GRCh38.p7	X:106725812	CTATCAGACAGCAGG[C/T]ATATTAATTCAGCTT	79589
rs781540939	snp	G/T			missense	RNF128	GRCh38.p7	X:106694025	AGGAGAATAGGTCCA[G/T]TTTTTTTTGGCTCCT	79589
rs781548224	snp	C/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106772462	AAATCCTTATACATG[C/G]TAGTAGTGAGCTCTT	79589
rs781554606	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106778673	ACCTAGTAAGCAGTC[C/T]CTTCATCTGAGTCTT	79589
rs781556054	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106769098	TTGTTATAATTTCTG[G/T]TCTTTTACATTTGCT	79589
rs781563084	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106734640	TATACATCCCAAAAA[A/G]GTACATAAATCATTG	79589
rs781576294	snp	G/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106720751	TGTGACCTTCAGCAA[G/T]ATACTTCATTTTTCT	79589
rs781646056	snp	A/G	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106783477	TCTAATTTTCATGTA[A/G]CATAAATGTCAGCTG	79589
rs781657503	in-del	-/TA	2.48645e-05	0.00352585	intron-variant	RNF128	GRCh38.p7	X:106772886	AATGTTTCACCAAAC[-/TA]AAACTGAATTTGTTT	79589
rs781663344	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106716304	CCAACGCAATAACAT[G/T]GATGAATCTCAACTG	79589
rs781669130	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106787429	AGTGGTTGCCAGGAG[A/G]TGGGGATGAGAGGAA	79589
rs781687097	snp	A/G			intron-variant	RNF128	GRCh38.p7	X:106760797	CGTGTATACAATGGA[A/G]TACTATTCAGCATTT	79589
rs781689107	snp	A/C			intron-variant	RNF128	GRCh38.p7	X:106766825	ATTTGCCTAGGTTTT[A/C]TTCTAGGATTTTTAT	79589
rs781703895	snp	A/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106794577	AGCCACTTCTTCAGG[A/T]GGCCTTTTACTGGAG	79589
rs781737272	snp	C/T	0.000529661	0.016265	intron-variant	RNF128	GRCh38.p7	X:106701922	CAGTTATTTAAAAAA[C/T]TGACATGATTATGGG	79589
rs781766181	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106743088	CCACTTCAAACAACT[C/G]TTTAACTTGAAGATC	79589
rs796197742	snp	C/G			intron-variant	RNF128	GRCh38.p7	X:106707475	GTATTGACATGTTGG[C/G]TTTTTTTCTTAACTA	79589
rs796775898	in-del	-/A			intron-variant	RNF128	GRCh38.p7	X:106750739	AGCATGACATCACAC[-/A]AAAAAAAAGAGAGAG	79589
rs797001782	snp	G/T			intron-variant	RNF128	GRCh38.p7	X:106756306	CCAAAAGAACAAAGC[G/T]GGAGGCATCACACTA	79589

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