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

RNF121

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs188912957	snp	A/C	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71951048	TGACCAACATGGAGA[A/C]ACCCTGTCTCTACTA	55298
rs189003747	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71989778	AACTTTGATGATATG[A/C]TACAGATTATTTATA	55298
rs189009840	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71970774	TATTTTTTTCTCTAC[C/G]TAAAGTTCAAAAATA	55298
rs189015742	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951737	GAAAAGAAGTCCAAC[A/G]TCATTTAGCTGTCAG	55298
rs189019269	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941147	CCAAGTCTAATTGAA[C/G]TTTGGAAGTTACTTT	55298
rs189024017	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71930642	ATTTCTGTGATTACA[A/G]TTGGCTGTGGTTCAG	55298
rs189192672	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968509	TAGCCATAGCTACCA[A/G]TTTTACAATTCTTGT	55298
rs189205797	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929471	GGACGTGAATTTCTT[C/T]AGGGGAAGGCTGGGC	55298
rs189257412	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71965437	TGTATTTTTTATAGA[A/G]ATGGTTTTATGTTGT	55298
rs189291826	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961283	TTTTAAAGAAGGATC[A/G]GGTGTGGTGGCTCAT	55298
rs189536704	snp	G/T	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71983794	TATGACAGAGGTTTG[G/T]GTAGGTCCAAGAGAG	55298
rs189547582	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947604	GATAGTTCAATGTGG[C/G]TGGAATGTAAGCCAT	55298
rs189576821	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980599	TGATCTACCTGCCTT[C/G]GCCTCCCAAAGTGCT	55298
rs189586565	snp	C/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71940473	GCATTAGGAATGAAC[C/G]CCCAAGGTCAATGTT	55298
rs189653266	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71991961	AAATGAGACAAAAAA[A/G]AAAAAAACCTAGCCG	55298
rs189659229	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972601	ATTCTTTTTTTCTCG[A/G]GGGCTGTCCTGTATA	55298
rs189674371	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71952997	ACTCAAAGAAAAAAC[A/G]TATTCCTCTTGTCTG	55298
rs189683306	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71932686	ACCAAGTGGTGTCAC[A/C]AAGATTTAAACCCAT	55298
rs189791343	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984346	CAGTGGCACGATCTC[A/G]GCTCACTCGTGCAAG	55298
rs189791739	snp	G/T	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71981472	TGTTGATGGCATCAG[G/T]AAGAAAACCTCCATT	55298
rs189832917	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975308	GCTGTGGTATCTTTA[C/T]CAGCCTCCTTTGAGT	55298
rs189944499	snp	C/T	0.00993419	0.0697739	intron-variant	RNF121	GRCh38.p7	11:71936461	GTGGCACGATCTCGG[C/T]TCACTGCAAGTTCCG	55298
rs189945457	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966639	GGTACACACCACCAC[A/G]CTTGGCTAATATATA	55298
rs190048978	snp	G/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71961974	TGCAAAGATTTTTTT[G/T]TTTTTTTTTTTGAGA	55298
rs190069417	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71994263	CTGCCACAAATGTCT[A/G]AGAATGCCCTTGTCA	55298
rs190088567	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956045	TCCAGTACACATACA[G/T]AAAGGATGCCTGGTA	55298
rs190166378	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71992279	GATTTAACCCACAGC[C/T]GCTACAACAACAGCC	55298
rs190182345	snp	C/T	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71973134	GAGGTTGTGGTGAGC[C/T]GAGACTGTGCCTTTG	55298
rs190408514	snp	A/G	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996471	CTGGGGAGGGATATG[A/G]TGGAGAGCCAGCCAG	55298
rs190412389	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71967820	TGTTTACATTATTAA[A/G]TATTATATGTAAGTA	55298
rs190417308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950146	AATTGTCTGAAATGC[C/T]AGGTTGCTCAGCCAA	55298
rs190419284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976530	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACG	55298
rs190426083	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF121, LOC100133315	GRCh38.p7	11:71928707	CTAGTCCCCACGTCT[C/T]GCTCCTTGGAGCCCA	55298
rs190487705	snp	C/T	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71952691	GCGCATGCCTGTAAT[C/T]CTAGCTACTCAGGAG	55298
rs190561615	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71942667	TACTCTGGAGGCTGA[A/G]GCAGGAGAATCGCTT	55298
rs190571160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991399	TATGCCAGAATTACA[A/G]AAGTGTACAAAAATA	55298
rs190589960	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71944720	TGAACTTGGGTGACA[C/T]AGTGACTCGAGAAGT	55298
rs190675636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981914	ATACTCTAGATAAGC[A/G]CTATAATAATGTTAG	55298
rs190742724	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71931292	AGCATTCATTCCAGG[A/G]ACCTTGTTACTTGTT	55298
rs190799345	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997368	CCCTGGGCCTGACAA[C/T]GGGAGTGGTGGGTGG	55298
rs190817488	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978728	CTGACATTATTAGGC[A/G]CTGTTGTAAGTGCTT	55298
rs190819159	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71959290	TACATTTTGTTATGA[A/C/G]AAACTTTAAACACAT	55298
rs190823765	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71972500	TTTAGTGGGCATCCA[A/G]TGACCACTGAGTGGA	55298
rs190833453	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939252	TTTTTAAGCATGTGC[A/C]GCAAAAATTCAGTCT	55298
rs190840465	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928511	GGAATGCGTTCTGGG[G/T]CTTCAAGAAGCTGCT	55298
rs190931905	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963287	AGAATCCATTGCCAA[A/G]TCCAAGGTCATAGAG	55298
rs191048296	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71981775	TTTCCTCTTACTTAT[C/T]GGAATTTATTGAGGA	55298
rs191065053	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71962915	TATAGCTACTTTAGT[A/G]GATGTAGATGTCATT	55298
rs191071926	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943486	TAAAATAATAAAGGC[A/G]TTTGTTACGCCAGCC	55298
rs191078568	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949696	CAGAGTAAGACTCCA[C/T]CTCAAAACACATGCA	55298
rs191129822	snp	A/C	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71933068	GGATAAGATGTGGGT[A/C]CCAGTTAGGTGGCCC	55298
rs191150749	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993708	CTTTTGGGTTTATAC[C/T]GAGAATGGAATTGCT	55298
rs191153046	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71974236	GTGAGCCACCACGCC[C/T]AGCCAAGCCCTGTTG	55298
rs191166594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955208	GAGCCCCAGGTCTCT[C/T]GCTTGCCCTATCCTG	55298
rs191170664	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71934710	TGTAAAATGAGTGGT[A/G]GCAAGTGTAGTGGGG	55298
rs191206420	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965413	GAGCCACCATGCCCA[A/G]CTCATTTTTGTATTT	55298
rs191333855	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986613	TCTACTAAAAAAAAT[A/G]TAAAAATTAGCCGGG	55298
rs191360626	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953265	TCTCAAATTCCTGGC[C/T]TCAAGAGATCCTCTG	55298
rs191397575	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938758	TAAGGAACAATTTTT[C/T]CCTTTTTGGTAGGAT	55298
rs191476855	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977638	GCTTTGTATTTGCAC[A/T]TTCAGGGAGAGAAGG	55298
rs191625190	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938397	AGATCTCTGCTCACC[A/G]TAACCTCCGCCTCCT	55298
rs191641761	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71958113	AAATATGCTGTCTGC[C/T]GTAAGAGAGGTGATA	55298
rs191665791	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994030	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	55298
rs191696857	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71989517	AAGTGGTGTAAGATC[A/G]ATGATTTCTAGTGAG	55298
rs191701674	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71969813	CTCAAGCAGTCCTCC[C/T]ACCTTGGCCTCTCAA	55298
rs191703564	snp	A/G	0.00755907	0.0610114	intron-variant	RNF121	GRCh38.p7	11:71964118	AATGTTTCCATCTTA[A/G]CAATATTAATCTTCC	55298
rs191705888	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997732	TTCCCAGCTGTTCCC[C/G]TGCTGACATCCCTAG	55298
rs191713169	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71951568	GGATTTGAGGCTCTA[A/T]TGTACAATGATCATG	55298
rs191716562	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945619	CATTTATTGAACACA[C/T]ACAGTATACCAGATT	55298
rs191723645	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930390	TGGACTTGGGAAGCA[A/G]TAAGACTGTTGCCTG	55298
rs191733941	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996936	TGACTTGGCCAACAA[A/G]GGAAGCCTTGGGGCC	55298
rs191922017	snp	G/T	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71967355	GTTTTTTTTGTTTTT[G/T]TTTTTTTTTTTTGAG	55298
rs191994569	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993117	TTATTGACAGTTTAT[G/T]AGGTTCCTTTTTGAA	55298
rs192032372	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71940253	TTCAGGGAATTTACA[A/G]TCTAGTTAGAAAAAT	55298
rs192036900	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71988121	TATTATCCCAGATAA[C/T]GCTGCTCTGTTGCTT	55298
rs192039571	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71968225	CCACCATGCCTAGCT[A/G]ACTCTTTGTATTTTA	55298
rs192047866	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71950863	GAAGGCCAGAGTATT[A/G]TAGCTCACTCCAGAA	55298
rs192094274	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71954286	GACTGGTTTGGATGT[A/G]ACTTAAATAACCTTT	55298
rs192195584	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71947646	TGGTGAAATAAGGTC[A/G]CTGGTTGGGCCATAT	55298
rs192217544	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986290	ATTCTACCTCTGATT[C/T]ATCTCTTGAATTCTG	55298
rs192462017	snp	A/C	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71973908	AGAAAATTTTGAAAA[A/C]TACAAAAAACAAAAG	55298
rs192466525	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983949	TCATTGTATAAGGTA[A/C]AATAGGTGATCCATA	55298
rs192500697	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71980815	AATGTAAAATAGATA[C/T]TTGATTTCAAAGCCT	55298
rs192540919	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983326	CCGTTTTGAGTATCT[A/G]TCTCCCTCACTAAAC	55298
rs192545930	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964985	TAGAGACAGGATGAG[G/T]TTTTCATTCTGCAAA	55298
rs192554970	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71946194	CATTACTCATAATAG[C/T]CCCAAGTAGAAATAA	55298
rs192585761	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71965603	TACCTTTATCGATTG[A/G]CTTGTTAATTAACAG	55298
rs192638293	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71936140	GCGTGAGATTATAGG[C/T]GTAAACTGCTGCGCC	55298
rs192697878	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71974640	AGGTTCCTCTCAAAG[A/G]CTTCAGGAAATTTTT	55298
rs192731045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959833	TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC	55298
rs192833333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980450	CTCCCGGATTCAAGC[A/G]ATTCTCCTGCCTCAG	55298
rs192865871	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955927	AGGAGGGATGTTGAC[G/T]TCATTACCTAGATTG	55298
rs192868800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982473	ATGGACACTGAATGC[A/G]GGGAGACTAAGAAAG	55298
rs192933588	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979808	TGAAAAACTGGCAGG[A/G]GAACAGGAGTTTCTG	55298
rs192991456	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71939533	GGGTCAAGTTAATAG[C/T]CAACCATTTTCACAG	55298
rs193012978	snp	C/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929258	ACTAGGGGGCGGGTG[C/T]GTGGAGAGCGAAGTC	55298
rs193046444	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959928	GGTGTGAGCCACCGC[A/G]CCCGGCCTCTAATTC	55298
rs193053615	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71968940	GCCCAGGCTGGAATG[C/T]AGTGGCGCGATCTCG	55298
rs193063749	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929995	GTGAGCTCCTTGAGA[C/T]TGTATGTTCCCTTTA	55298
rs193232439	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71951122	TCAACTACTCGGGAC[A/G]CTGAGGTGGGAGAAT	55298
rs193253012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989106	TTTGTTTGTTTTGAG[A/G]TGGAGTCTTGCTTTG	55298
rs193295788	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71933269	CTGTGAATCTGGATG[A/G/T]GTCCACTCTCAAGTC	55298
rs199545883	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71931496	TTCTACTAATGTCTC[C/T]CCAGCTGTTTCTTTG	55298
rs199553501	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71942789	ATATATATATATATA[G/T]AGATATATATATGTA	55298
rs199675182	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71948159	AATAGGAATTTGATG[G/T]GATAGCAATTGAAGA	55298
rs199684147	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71957317	GCAGGTTAACCCAGC[C/T]TAATTGAGTGATATG	55298
rs199753748	in-del	-/AAT			intron-variant	RNF121	GRCh38.p7	11:71951221	TCTCAAAAAAAAAAA[-/AAT]GCAATAATGAAAGTC	55298
rs199763160	snp	A/C	0.000690584	0.0185692	intron-variant	RNF121	GRCh38.p7	11:71960709	TCCCTTTATCACTAC[A/C]GCATCCCTGACTTGA	55298
rs199771921	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71974463	CTCTTGGAACCTCCT[A/G]ACAGCTCTGTAAGGT	55298
rs199790572	in-del	-/T	0.0376037	0.131863	intron-variant	RNF121	GRCh38.p7	11:71963628	TTCCCAAAAAAAAAA[-/T]GAGTTTTATAGTCTT	55298
rs199822208	snp	A/G	0.000101434	0.00712085	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996351	AAACCCACCCCACAC[A/G]CCATGGACCTCAGGG	55298
rs199955313	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976525	TATGCCCAGCTAATT[C/T]TTGTATTTTTAGTAG	55298
rs199994585	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71986786	AAAAAAAAAAAAAAA[A/G]AAAGAAAAAAAATAC	55298
rs200015957	snp	A/C/T			intron-variant	RNF121	GRCh38.p7	11:71974669	TTGTCAATTTCTGCC[A/C/T]TAGTCAGAAGTTTTT	55298
rs200036412	in-del	-/TAAAA			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926946	TAAAATAAAATAAAA[-/TAAAA]GACAAATAATTATAC	55298
rs200123731	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71992289	ACAGCCGCTACAACA[A/C]CAGCCACTGTCACTT	55298
rs200184330	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995363	GAGCTGATAAAGAGC[A/G]AAGGCAGGATTTGAA	55298
rs200245164	snp	C/T	1.64762e-05	0.00287016	intron-variant	RNF121	GRCh38.p7	11:71957280	GTAAGTGTGGTAGTT[C/T]GGGCCCTGCAGTCTA	55298
rs200253473	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969859	GGCATGAGCCACCGT[A/G]CCAAGCCAAAACCAC	55298
rs200323104	in-del	-/A	0.0341408	0.126114	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927094	CCACAAAATATTTTT[-/A]AAAATTAGCCAGGTG	55298
rs200466536	snp	A/G	0.0452528	0.143452	intron-variant	RNF121	GRCh38.p7	11:71988652	TCTTAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	55298
rs200467525	snp	C/T	0.00498756	0.0496881	missense, intron-variant	RNF121	GRCh38.p7	11:71995447	TTGACCAGCGGTGCT[C/T]AGCTTCCACGAGTTC	55298
rs200498282	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970308	TAGTAATACATAACA[G/T]TATTGAACTGTATAC	55298
rs200503159	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71954248	TTACTCCTTCCCTTA[-/T]TTTTTTTTTACTTGA	55298
rs200563413	in-del	-/AG			intron-variant	RNF121	GRCh38.p7	11:71942783	TCTGTATATATATAT[-/AG]ATATATAGATATATA	55298
rs200610641	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71991091	AGGGAGTGGGGACAA[A/C]GGTTGAAAAACTATC	55298
rs200643002	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71948946	GCTGAACCTACCAGG[A/C]TTCATGAGCTAGCTA	55298
rs200667512	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71966185	CCACCATGCCCAGCT[A/C]ATTTTGTATTTTTAG	55298
rs200780950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978558	TGTGTGACTTAATGC[A/G]TTTTTAATCATGCAA	55298
rs200825356	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71942793	ATATATATATATAGA[G/T]ATATATATGTACACA	55298
rs200831971	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71942791	ATATATATATATATA[C/G]ATATATATATGTACA	55298
rs200870132	in-del	-/G	0.0103356	0.0711407	intron-variant	RNF121	GRCh38.p7	11:71967358	TTTTTGTTTTTTTTT[-/G]TTTTTTTTTGAGACG	55298
rs200948289	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71973198	CTCAAAAAAAAAAAA[-/A]GAGGGAAATGTAGGC	55298
rs200999189	snp	C/T	0.00203774	0.0318547	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929020	GAGCAGCGGAAGCAG[C/T]TGGCTCGCGCGGGGA	55298
rs201080311	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71989860	ATTTTATCTTTTTTT[-/T]CTTAAACCTGTGTTT	55298
rs201169900	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954950	TTCCACAAGTACTCA[C/T]TGAGTGCTTAATATA	55298
rs201232790	snp	A/G	1.6525e-05	0.00287441	intron-variant	RNF121	GRCh38.p7	11:71957178	ACCTTATATTGGCAG[A/G]GACAGTTTTAAGACA	55298
rs201445177	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990713	ACATGGCATCTACCA[C/T]AGGGGTAAGTTCATC	55298
rs201461768	in-del	-/CTG			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928032	AGGTATCGAGTTCAC[-/CTG]CGGCTGCTGAAAAAT	55298
rs201489498	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71974027	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	55298
rs201521523	snp	A/G	0.00226142	0.0335499	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929044	GCGGGGACTGCGGTG[A/G]GGGGGCGAGCCGTGA	55298
rs201538961	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71957316	TGCAGGTTAACCCAG[C/G]TTAATTGAGTGATAT	55298
rs201565303	snp	A/G	6.62285e-05	0.00575412	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982798	GGGTTGTTCCCCTCT[A/G]TTTCACAGTGAAGCT	55298
rs201611382	snp	G/T	3.32989e-05	0.00408024	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996160	CACTCCTGGCAGCTC[G/T]TGCACAGAGTCTCTT	55298
rs201688560	snp	C/T			utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929084	CAGTGGTGGAGGTGG[C/T]GGTTGGAGGTGGTGC	55298
rs201746342	snp	A/G	0.000988044	0.0222046	intron-variant	RNF121	GRCh38.p7	11:71957271	GCAATGGAGGTAAGT[A/G]TGGTAGTTCGGGCCC	55298
rs201855470	snp	A/G	3.30464e-05	0.00406474	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996293	TAGTCCAAGGCATCA[A/G]CTACATCCTGGGCCT	55298
rs201859304	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71985941	TAGCCAAAAAAAAAC[-/A]AAAAAAAAAGGCCCT	55298
rs202044759	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71930543	ACCTCCCAATCACTA[A/G]AGACTACAGGTGTTT	55298
rs202044944	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71984178	AGAAAAAGTGCAATA[C/G]AACAATGTAAGAGTC	55298
rs202048779	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938793	TCAGTGTGGCAGGGG[A/G]GCTCATGTATAGGTT	55298
rs202051338	in-del	-/GAGC			intron-variant	RNF121	GRCh38.p7	11:71964443	TCATCTGAGAGTAGA[-/GAGC]GTTTCACTTCTTCTT	55298
rs202073512	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71981215	CACCACACCCGGCTA[A/T]TTTTTTTTGTATTTT	55298
rs202143487	snp	A/G	0.000102801	0.00716869	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929141	TAAGCGGAGTTGAGA[A/G]ACGAGGAGAGACTCA	55298
rs202159165	snp	A/G	0.00199792	0.0315431	intron-variant	RNF121	GRCh38.p7	11:71994867	TGTATCCTGCCTCGA[A/G]CTCCTGGGCCACATC	55298
rs202223294	in-del	-/TTTG			intron-variant	RNF121	GRCh38.p7	11:71989071	TCTGCATTATGGTTT[-/TTTG]TTTGTTTGTTTGTTT	55298
rs367564185	snp	C/G/T	3.33718e-05	0.00408473	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996149	CCATGCTAGATCACT[C/G/T]CTGGCAGCTCTTGCA	55298
rs367653048	in-del	-/AG			intron-variant	RNF121	GRCh38.p7	11:71986789	AAAAAAAAAAAAAAA[-/AG]AAAAAAAATACAAAG	55298
rs367671346	snp	A/G	1.67517e-05	0.00289406	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996336	AAGAGCATCAGTGGA[A/G]AACCCACCCCACACG	55298
rs367673376	snp	C/T	6.7667e-05	0.00581626	intron-variant	RNF121	GRCh38.p7	11:71960747	CATGTGTTTGGCTTT[C/T]AGGGTCGAGCACGCA	55298
rs367725611	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71969185	AGCCACCGTGCCTGG[A/C]CCCTCTTAGGATTTT	55298
rs367729587	snp	C/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928886	GCACGGTACTCCCCT[C/T]TCCTTGACCCTGAAA	55298
rs367770176	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71984044	AGATGAATGTGGATT[G/T]GGACCCCTAGCCCTG	55298
rs367784677	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71934941	TGTTCCAAATGCATT[-/C]TTTTTTTTTTTTTTT	55298
rs367968910	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71961433	AGGCGTGGTGGCATG[C/T]GCCTATAGTCTCAGC	55298
rs367990312	in-del	-/G	0.00953873	0.0683987	intron-variant	RNF121	GRCh38.p7	11:71963224	TTGATGAAGTTCAGT[-/G]ATATCTATTTTTTAA	55298
rs368035201	snp	C/T	0.000228302	0.0106817	missense, intron-variant	RNF121	GRCh38.p7	11:71995440	ATTTCCCTTGACCAG[C/T]GGTGCTCAGCTTCCA	55298
rs368054102	snp	C/T	1.64732e-05	0.0028699	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994828	GGATCATTGAGAACA[C/T]GTATAGGCTGTCCTG	55298
rs368061775	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71936408	CACTTTTTTATTTTT[G/T]AGACAGAGTCTCGCT	55298
rs368087714	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996000	CAGGCTGTGAGGAGG[-/AA]GAGGAGGGGGAGGGC	55298
rs368150981	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71961128	AAAAGATAGGTTTTC[C/G]CTTCGAAACATTGTG	55298
rs368163406	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71982709	TTTGGGACTGTGGAC[A/G]GAGCTGCAGAGGGAG	55298
rs368220887	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71944578	GTAAAACTGGAAAGA[C/G]AGCTAGGGGTCAGGT	55298
rs368223999	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938139	TCTGTTACTTAGAAG[C/G]CTCAACATTTTACTC	55298
rs368249883	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929171	AACCTGAGACTGAGG[A/G]GAGGGGCAGTGAGGT	55298
rs368325381	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71960462	GGACCTCCTTCATGC[C/T]ACAGGAAAGGTGTCA	55298
rs368347778	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71943838	CATGTGCAAGGTGGG[A/G]GGTGAGAAAGAGAAT	55298
rs368350624	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71965888	TTTTTAATCTTTGTC[A/G]GTGTGATAAGGTGAA	55298
rs368421573	snp	A/G	0.000236927	0.0108815	intron-variant	RNF121	GRCh38.p7	11:71960930	CTTTGTCTGTCAGTC[A/G]TCAAGAGACCCTTCC	55298
rs368450412	in-del	-/AA	0.0126979	0.078662	intron-variant	RNF121	GRCh38.p7	11:71939806	TGTGCACTTAATTAT[-/AA]GCCAGGTACTCTTTT	55298
rs368508269	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968873	CCTCCTAGGATTTTT[C/T]TTTTTTCTTTCTTTC	55298
rs368586037	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71932070	CTTTTCTCTTTTTTT[-/T]GTCTGGTTTCATTAA	55298
rs368646464	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996562	AAACCTTTTTTTATT[A/G]TGGAGCATAGGAATT	55298
rs368656006	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71956454	TTCCTCAACAGGGAA[G/T]GAACCACCCTAAAAT	55298
rs368693196	snp	C/T	0.00019192	0.00979404	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929066	GAGCCGTGAAGATGG[C/T]GGCAGTGGTGGAGGT	55298
rs368986250	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942228	ATGAACCACCGTGCC[C/T]GGCAATGAAAAGATT	55298
rs369033088	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71973508	AAACAAAAAACAGGC[C/T]GGGCGCGGTGGCTCA	55298
rs369035487	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71985383	TCTCAAAGAGGTGAT[C/T]TGACTTATCTGAGGT	55298
rs369048798	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963798	GTCGTGGCATGTCAC[A/G]ACCTTGTCAGAAATC	55298
rs369068934	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71945972	AAAAAATAGCCAGAC[A/G]TGGTGGCTCGTTTCT	55298
rs369100997	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71992843	ATTTCTATTTTTTTT[G/T]TCAGAATGGAAATAT	55298
rs369223579	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983998	GTAGTTTACTTTAAA[A/G]GCCACTGTGGAAGAT	55298
rs369401355	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71988920	TGAAGGAATAAACAG[C/G]CTCCTGAAGGGTTTA	55298
rs369628902	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996580	GAGCATAGGAATTGC[C/T]CCCCTCCAGGCTTCA	55298
rs369634116	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982128	GGTCGGGGCCATACC[A/G]TGGGGGATTTGACAG	55298
rs369643026	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973558	TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTGAG	55298
rs369702838	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71980494	TGGGATTATGGGTGC[A/C]CGCCACCATGCCTGG	55298
rs369711967	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71979486	CTTGATATAGCTTTA[C/T]GTACTTGATGTATAT	55298
rs369751219	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968888	CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	55298
rs369775219	snp	C/T	3.3e-05	0.00406189	intron-variant	RNF121	GRCh38.p7	11:71987124	CAAGTGAGTACCCTT[C/T]GTTTTTGTTTTTGCT	55298
rs370033904	snp	A/G	1.74184e-05	0.00295109	intron-variant	RNF121	GRCh38.p7	11:71982953	GAGCCCAGGTTTTCC[A/G]AAGCTAATGGGTTGG	55298
rs370145143	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71954613	AAGTCTTATTTCTCT[A/G]TTTTCTAGATGGAGA	55298
rs370174105	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71968596	CAGAGCATAAATATA[C/G]TTGGGACATTACCAC	55298
rs370291265	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976493	CCCGAGTAGCTGGGA[C/T]TGCAGGTGTGCGCCA	55298
rs370358136	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71954992	GTGCTGTTCTCCTTG[A/G]AAGACATAAATCACT	55298
rs370375234	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71948806	GGGGAAGAATGTGAA[C/T]GAGAGGAGAATGGGG	55298
rs370415897	in-del	-/ATT			intron-variant	RNF121	GRCh38.p7	11:71934938	AAGTGTTCCAAATGC[-/ATT]CTTTTTTTTTTTTTT	55298
rs370470198	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71954621	TTTCTCTATTTTCTA[-/G]ATGGAGAAACTAAGC	55298
rs370471232	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71948341	GTCAACGTGGTGAAA[C/T]CCCATCTTTACTAAA	55298
rs370477935	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992113	TGTCTCTAAATAAGT[A/T]AAAATTCACAAAATG	55298
rs370583452	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994537	AGCAAAGATGAGGTC[A/G]ATTTGACTTGTAAAA	55298
rs370587050	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931961	CTTTGGAAAGAAGTT[A/G]CACGCTGTGTATATT	55298
rs370815226	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71990537	GTGTGTCCCAGAGTA[G/T]TAATCCATAGAAGAT	55298
rs370833573	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71968108	GCTCTGTCGCCCAGT[G/T]TGGAGTGCAGTGGCA	55298
rs370844229	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948070	GGGTAAAAAGTTTGA[C/G]TATATGGAAAGCTGC	55298
rs370902927	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938603	GGATTACAGGCGTAA[A/G]TCACTGCTCCCGGCC	55298
rs370960988	snp	A/G	0.000148794	0.00862407	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960776	CACGCATGCATGCCA[A/G]GCACCGTGGCCATGA	55298
rs370988382	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71960002	AGGAGTGACTGTTCT[C/T]AGAACAAGTTTTTAG	55298
rs371035473	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947089	CATGTGGTCTCAACC[C/T]CCTGACCTCAGATGA	55298
rs371135660	snp	C/T	1.65083e-05	0.00287296	intron-variant	RNF121	GRCh38.p7	11:71994692	TCACATCTTTTCCTA[C/T]CTTTCCTTCCTGCTA	55298
rs371140470	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987735	CTGACTCTTGGGCTA[A/G]ACCGTCTACCTACAT	55298
rs371214589	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71956207	AGGAATGGTTGTTGA[C/T]TGATTTGAGTATTTC	55298
rs371225978	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71993707	TCTTTTGGGTTTATA[C/T]CGAGAATGGAATTGC	55298
rs371295709	snp	A/G			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996715	GGCCTCAGCCCACCC[A/G]CTCCCTTCTTCCCTG	55298
rs371406502	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71934924	CCTAGTCCTGTGCCA[A/C]GTGTTCCAAATGCAT	55298
rs371425432	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997205	AAGAGTGCGTATGCG[C/T]GTGTGTGTGTGTGTG	55298
rs371521377	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976584	AGTATGGTCTCGATC[C/T]CTTGACCTCGTGATC	55298
rs371605528	snp	C/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997353	TCATTCATGGGTCCT[C/G]CCTGGGCCTGACAAC	55298
rs371607441	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71956836	AAGCCTTCCCTAGTC[C/T]AAAACACCCCAGATT	55298
rs371624677	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71944241	GGGAGACTGAGGCAG[G/T]AGAATCACTTAAAGC	55298
rs371649136	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71983416	CCATGGGGCCTGGCA[A/C]ATAGTAGCCTGCTCT	55298
rs371694671	snp	A/C/G	1.7159e-05	0.00292903	intron-variant	RNF121	GRCh38.p7	11:71982938	TTTAAGTAGTGGGAA[A/C/G]AGCCCAGGTTTTCCG	55298
rs371703060	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71956667	GTTATATCTAACTCT[-/T]GTCTCCCACTAATCC	55298
rs371720265	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71971898	ATACACATACCCTGT[C/G]ACACATCCTAAGGGG	55298
rs371808017	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71957318	CAGGTTAACCCAGCT[A/T]AATTGAGTGATATGT	55298
rs371887600	in-del	-/TGATT			intron-variant	RNF121	GRCh38.p7	11:71932877	TTTAACTTACTGATA[-/TGATT]ACTGGTGGATTCTGC	55298
rs371966062	snp	G/T	0.000576868	0.0169735	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929040	TCGCGCGGGGACTGC[G/T]GTGAGGGGGCGAGCC	55298
rs371989729	snp	A/G	1.64757e-05	0.00287012	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994846	ATAGGCTGTCCTGCA[A/G]TCATGTGTATCCTGC	55298
rs372005344	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71934736	TGGGGAAAAAGCCAT[A/G]GGGTAGTAAACAGTG	55298
rs372019479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976638	GCTGGGGTTACAGGC[A/G]TGAGCCACGGCACCT	55298
rs372075971	in-del	-/A	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71946767	CCCAGGCTGGAGTGC[-/A]AGTGGTGCAGTCTCA	55298
rs372116180	snp	C/G	0.00835141	0.0640778	intron-variant	RNF121	GRCh38.p7	11:71950949	CAATAATGAGGCTGG[C/G]TATGGTGGCCCACAC	55298
rs372117578	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71962627	AATGCTGAATTTTAT[A/T]GGTGAGAGGATATGC	55298
rs372205906	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949990	TGGGCGACAGAGCAA[A/G]ACTCCATCTCAAAAA	55298
rs372328505	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71966387	AGTTCTACAAGACTT[C/G]AGAAGCAAAACACAT	55298
rs372344877	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934874	TAGCAGAAAAGAGTG[C/T]TGAGGGTGAAATAAT	55298
rs372354627	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956541	CGAGAACTTTGAAGT[A/C]GGATGGCTAGTGATA	55298
rs372372273	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71986790	AAAAAAAAAAAAAAA[-/G]AAAAAAAATACAAAG	55298
rs372422273	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968880	GGATTTTTCTTTTTT[C/T]TTTCTTTCTTTTTTT	55298
rs372440308	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71995965	CACCTTCTCTGCATT[C/T]AGCTCTTTACCCCAA	55298
rs372451541	snp	C/T	0.000218386	0.0104473	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996341	CATCAGTGGAAAACC[C/T]ACCCCACACGCCATG	55298
rs372482710	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929599	ATCTTAAAGTTGGAA[C/T]TGTTTTATTTATCGT	55298
rs372484163	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950520	ACCCAGGAGGTGGAG[A/G]TTGCAGTGAACCGAG	55298
rs372505806	in-del	-/C	0.0142736	0.0832652	intron-variant	RNF121	GRCh38.p7	11:71991192	TGCCCATGTAACAAA[-/C]CTGCACATGTACCCT	55298
rs372513453	in-del	-/AGCAGCTGT			intron-variant	RNF121	GRCh38.p7	11:71948613	GCAGGCAGCAGCTGT[-/AGCAGCTGT]TAGAGCCAACATCTA	55298
rs372586776	snp	C/T	1.65501e-05	0.00287659	intron-variant	RNF121	GRCh38.p7	11:71990743	CCGGGTTCTTAAATA[C/T]TGCTTCTTGACACCT	55298
rs372647587	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71982208	ACACGTGGTGGCACG[C/T]GCCTGTAATCCCAGC	55298
rs372675094	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71940141	CTAATCCTTGAGCAT[A/G]TGATTCCTCACTAAT	55298
rs372713354	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71946355	CATTTTGATGAGTGA[A/C]AGAAGACAGTCACAA	55298
rs372816511	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71944858	CCAGCCATGAACTTT[C/G]GTTTTCCCTTCTCCC	55298
rs372969078	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963313	TAGAGATTACTCTTA[C/T]GTTTTCTTTGAAGAG	55298
rs372972760	in-del	-/AGG			intron-variant	RNF121	GRCh38.p7	11:71941184	GATCAGGTTGGAAAA[-/AGG]AGAATAAATCAGTTA	55298
rs373012213	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71995562	AATCCGTATCCTTTA[C/T]TGGGGTCGTTGTTGG	55298
rs373014603	snp	C/G	3.32171e-05	0.00407522	intron-variant	RNF121	GRCh38.p7	11:71987157	AGTTTGGGGAGGAGT[C/G]ACTGTTGAGATGTAC	55298
rs373047681	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71962844	TTTTCATTCCTCCAC[A/G]TTCTTATCAAGACTT	55298
rs373049753	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981113	GAGTGCAGTGGTGTG[A/G]TCTCGGCTCCCTGCA	55298
rs373061842	snp	C/T	9.98652e-05	0.00706559	splice-donor-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929126	GGGAGCTGGATGAGG[C/T]AAGCGGAGTTGAGAG	55298
rs373196085	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71967026	ACAGGCACCCGCCAC[C/T]GCGCCCGGCTAATTT	55298
rs373205293	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983410	GCCCTGCCATGGGGC[C/T]TGGCACATAGTAGCC	55298
rs373259400	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954157	AGTTAATGCTTGGCC[C/G]CAAATGAATAAACTC	55298
rs373262124	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71984992	AGTGCCATGATCACA[A/G]CTCACTGCAGCCTCA	55298
rs373292280	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980679	GCCACAGAGAAATCT[A/G]TAAGAGAATGGTAGC	55298
rs373329690	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71992841	ATATTTCTATTTTTT[C/T]TTTCAGAATGGAAAT	55298
rs373399403	in-del	-/ACAG			intron-variant	RNF121	GRCh38.p7	11:71971595	ACAAATCAACAAAAG[-/ACAG]CAACTCCAATAGAAA	55298
rs373439500	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71957863	AGAGTGCCTGCCCCA[C/T]GAACTTCACAAGGTG	55298
rs373447136	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927161	GTTGAGGTGGGAGAA[C/T]TGCTTGAGCCTGGGA	55298
rs373508723	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947533	AAGGTGAGTAGAGAA[C/T]TCTAGAGAGAAAAGA	55298
rs373651746	snp	A/C			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929949	TAAATAAGTGTCTCT[A/C]TCTTCTTCTGGATTT	55298
rs373661417	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976277	CAAGCCCTGATCCTA[A/G]GGTCCCAGAGATACT	55298
rs373758192	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71963195	TGTCCTTTGATGCAT[A/C]AACAGTTTTTAATTT	55298
rs373851565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961193	TATTCAATTGGAGAG[A/G]GCAAAGATGAATTGA	55298
rs373981798	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961029	ATGTATGAATGATGA[A/G]TAGTGTATTGGCGAG	55298
rs374008711	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71991500	TAAAAATAAAATTAC[A/G]ACTTTAATAAGCATT	55298
rs374152322	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71968935	GTGTTGCCCAGGCTG[G/T]AATGCAGTGGCGCGA	55298
rs374164862	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71943681	ATAATATGAAGAAGC[A/G]GAGATTTCAGGGAGC	55298
rs374173236	snp	A/G	3.29457e-05	0.00405854	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994747	CGGGCATGCCTACCA[A/G]ACATCTTTCAGACAG	55298
rs374371060	snp	C/T	1.68057e-05	0.00289872	intron-variant	RNF121	GRCh38.p7	11:71960912	CCACTTTGCCTCTTA[C/T]TTCTTTGTCTGTCAG	55298
rs374375105	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71987442	CAGAGCTGTTTTTCT[C/T]GTCAGTGTGTACTGT	55298
rs374493484	in-del	-/TTT			intron-variant	RNF121	GRCh38.p7	11:71938314	TGTGTAGTCTCTTAA[-/TTT]TTTTTTTTTTTTTTT	55298
rs374546857	in-del	-/CTC	0.000362558	0.0134591	intron-variant	RNF121	GRCh38.p7	11:71994710	TTCCTTCCTGCTATT[-/CTC]CTTCAGTTCTACAGC	55298
rs374579709	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71937147	TTCTGCTCCCGTAGC[A/G]CCCTGTACAGATTTC	55298
rs374646984	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939441	CCTCCACCCCTATGG[A/C]CTGGGCAGTTTCTTG	55298
rs374731734	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71935404	AAGACTACTTCAGTG[C/T]TTGTGCTGTTAACCA	55298
rs374753695	snp	A/G	1.68199e-05	0.00289994	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982905	AAACCTCTAGTACAG[A/G]CAACCCCAAGGTGAG	55298
rs374942964	snp	A/G/T	4.85755e-05	0.00492802	utr-variant-3-prime, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995538	GTAGACCTCAAGAGG[A/G/T]TGTTCAGCAATCCGT	55298
rs374956143	in-del	-/AAAAAAAAA			intron-variant	RNF121	GRCh38.p7	11:71982346	ATCTCAAAAAAAAAA[-/AAAAAAAAA]GGAATGTTGGATCCT	55298
rs374963756	snp	C/G/T	5.15144e-05	0.00507494	intron-variant	RNF121	GRCh38.p7	11:71960727	ATCCCTGACTTGATT[C/G/T]ACCCCATGTGTTTGG	55298
rs374984580	snp	A/G	9.98768e-05	0.00706601	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996321	CCTGGAATAGTGATG[A/G]AGAGCATCAGTGGAA	55298
rs375019622	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934359	ATATGTCACAGGTGC[C/T]GTGATAGTGGGGTGG	55298
rs375045740	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71970069	AAAGTAAAGAAATTA[C/T]GTCATGTGGTACAGG	55298
rs375190407	in-del	-/AGGACTGGT			intron-variant	RNF121	GRCh38.p7	11:71957383	TGGCTCATGACCGGT[-/AGGACTGGT]CTTTTGGGATCTCTC	55298
rs375282295	snp	C/G/T	0.0006271	0.0176962	intron-variant	RNF121	GRCh38.p7	11:71995394	CCTTTCAAAGACTGT[C/G/T]TGGGGCTGGAGTGCC	55298
rs375334855	snp	A/C/G			intron-variant	RNF121	GRCh38.p7	11:71936063	CGTGTTAGCCAGGAC[A/C/G]GTCTCCATCTCCTGA	55298
rs375383986	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71993479	ATATTTGTCCCTTTG[G/T]CTTTTTTCACTTAGC	55298
rs375394937	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71935406	GACTACTTCAGTGCT[C/T]GTGCTGTTAACCACA	55298
rs375474913	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71989746	CCTTCTTGTTAAATA[A/G]ACTTGGACCAAAATT	55298
rs375480408	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976938	TTTCTTCTATTTTCC[A/G]TGTTCACTGCCTCCC	55298
rs375505999	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981942	TAGAAAAGAAAATGC[A/G]TTTGGAGCACTAGAA	55298
rs375507970	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952165	ACTACAGTACATGCT[A/T]CAAAGTGGATGAACC	55298
rs375513323	snp	A/G	3.29522e-05	0.00405894	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994728	CTTCAGTTCTACAGC[A/G]AGTCGGGCATGCCTA	55298
rs375558651	in-del	-/AGCTCTCA			intron-variant	RNF121	GRCh38.p7	11:71953583	TTCTGTTTCTTAACA[-/AGCTCTCA]GGGTACTCTTGGTGC	55298
rs375602656	snp	A/G	0.000260768	0.0114156	intron-variant	RNF121	GRCh38.p7	11:71995410	TGGGGCTGGAGTGCC[A/G]CCCTGGCTCTCACCA	55298
rs375655059	snp	C/T	0.000116054	0.00761668	intron-variant	RNF121	GRCh38.p7	11:71990754	AATACTGCTTCTTGA[C/T]ACCTCCAAATTGCTC	55298
rs375661763	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71982335	AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	55298
rs375681453	snp	C/T	0.000153988	0.00877327	intron-variant	RNF121	GRCh38.p7	11:71986959	CAGGACCATTAAGGC[C/T]AGAATCTCTGTGTCA	55298
rs375711695	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930203	TCTTGCACATGCCAG[C/T]ATATGGGCAAAGACA	55298
rs375902499	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931077	GACCTCAGGTGAGCC[A/G]CCGATCTTGTCCTCC	55298
rs376056779	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71964445	CATCTGAGAGTAGAG[A/T]TTCACTTCTTCTTTT	55298
rs376086660	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991622	CTATGGAGCTGACTT[A/G]AACAATGAATAGCAG	55298
rs376104254	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71948652	CTTTCACTTCACTGC[C/G]CAAAGTGTGCCACCC	55298
rs376137866	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71967484	CCTCCCAAGTAGCTG[A/G]GACTACAGGTTCATG	55298
rs376143838	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71947837	TTAGAGTCGGGGAGA[A/T]CATTTTGGAGGCCAC	55298
rs376156595	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927260	TCACTCAGGCTGGGC[A/G]CAGTGGTTCACACCT	55298
rs376190587	snp	C/G/T	0.0064842	0.0566137	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929050	ACTGCGGTGAGGGGG[C/G/T]GAGCCGTGAAGATGG	55298
rs376195118	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981474	TTGATGGCATCAGGA[A/G]GAAAACCTCCATTAT	55298
rs376209063	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967037	CCACCGCGCCCGGCT[A/G]ATTTTTTGTATTTTT	55298
rs376289574	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959925	ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCTCTAA	55298
rs376309998	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966482	TTTTAGTTCATTTCT[A/G]ATACTTTTTTTTTTT	55298
rs376316883	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968783	AAAAACAGTTTCAAA[C/T]TGTTTTTAAATTAAA	55298
rs376331292	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71962913	ATTATAGCTACTTTA[G/T]TGGATGTAGATGTCA	55298
rs376423109	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71992842	TATTTCTATTTTTTT[A/T]TTCAGAATGGAAATA	55298
rs376450806	snp	C/T	1.73945e-05	0.00294906	intron-variant	RNF121	GRCh38.p7	11:71982952	AGAGCCCAGGTTTTC[C/T]GAAGCTAATGGGTTG	55298
rs376468791	snp	A/G	6.70815e-05	0.00579105	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960754	TTGGCTTTCAGGGTC[A/G]AGCACGCACGCATGC	55298
rs376492085	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71974013	GTGGCGCTATCTCGG[C/T]TCACTGCAAGCTCCG	55298
rs376667004	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71991118	TATCTGTTAGGTAAC[C/T]GTGCTCATTACATGG	55298
rs376723210	snp	A/G	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71944653	GGAGGGCATTGTGTA[A/G]TCTACTAAGGAGTTC	55298
rs376826734	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929835	AGACAGACAAGAAGA[C/G]TAGTCATTGCATTAG	55298
rs376945162	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71975067	ACTACCAAATATAGT[A/G]TCTCTTCACATCTCT	55298
rs377022300	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71943149	CAGGGATAGCAGAGA[C/T]GATGGAGAAAAGTGG	55298
rs377025326	snp	A/G	0.000437904	0.0147905	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929187	GAGGGGCAGTGAGGT[A/G]TCGGGAGGTGGGGGT	55298
rs377191212	snp	A/G	0.000153988	0.00877327	synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71990693	TGCAGAAATGTGTGC[A/G]GACTACATGGCATCT	55298
rs377257567	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968884	TTTTCTTTTTTCTTT[C/T]TTTCTTTTTTTTTTT	55298
rs377347649	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71986105	ACCACCACCACACAC[A/T]TTCATCCAACTCAAA	55298
rs377348062	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954279	GCAGGAAGACTGGTT[C/T]GGATGTAACTTAAAT	55298
rs377489893	in-del	-/AGAG			intron-variant	RNF121	GRCh38.p7	11:71964441	GGTCATCTGAGAGTA[-/AGAG]GAGTTTCACTTCTTC	55298
rs377544751	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71964482	GATACCTTTTTTTTT[-/T]CCTGAGACAAGGTCT	55298
rs386374123	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71946868	AGGTGCTCTGGCTCT[-/TT]TTTTTTTTTTTTTTT	55298
rs386374124	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71946886	TTTTTTTTTTTTTTT[-/TT]TGAGACAGTATCGCT	55298
rs386374126	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71984939	CACTTTTTAAAAATA[-/A]GAGATGAGGTCGCAC	55298
rs386754839	multinucleotide-polymorphism	GC/TT			intron-variant	RNF121	GRCh38.p7	11:71949156	GGCATGGTGGTTCAC[GC/TT]CTGTAATCCTAGCAC	55298
rs386754840	multinucleotide-polymorphism	CCTGTAAAAATTTTTCCTGTAAAATGA/TTTTTAAGATGGAGTCTAACACTCTGT			intron-variant	RNF121	GRCh38.p7	11:71980358	AATGACACTTTTTTT[lengthTooLong]CACCTAGGCTGGAGT	55298
rs386754841	multinucleotide-polymorphism	CT/TG			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996419	AAAGACTCAAAGGGG[CT/TG]CTTGGGCCACTCAGG	55298
rs397701365	in-del	-/AAAAA	0	0	intron-variant	RNF121	GRCh38.p7	11:71982354	AAAAAAAAAAAAAAA[-/AAAAA]GGAATGTTGGATCCT	55298
rs397724016	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71947495	CTCAAAAAAAAAAAA[-/A]GGAATTGGGCAGTGA	55298
rs397730150	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71991246	TTATTAAAAAAAAAA[-/A]TTAGCCAGATCTCAG	55298
rs397750719	in-del	-/AGAG	0	0	intron-variant	RNF121	GRCh38.p7	11:71964444	CATCTGAGAGTAGAG[-/AGAG]TTTCACTTCTTCTTT	55298
rs397828827	in-del	-/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71968079	GATCTTTTTTTTTTT[-/T]AAGATGAAGTCCTGC	55298
rs397952111	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71988655	AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA	55298
rs398016596	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71948948	ATTAGCTAGCTCATG[-/A]AACCTGGTAGGTTCA	55298
rs398016597	in-del	-/TT	0	0	intron-variant	RNF121	GRCh38.p7	11:71951222	ACTTTCATTATTGCA[-/TT]TTTTTTTTTTTTTGA	55298
rs398016598	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71957318	ACATATCACTCAATT[-/A]AGCTGGGTTAACCTG	55298
rs398016601	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71980362	GTTAGACTCCATCTT[-/A]AAAAAAAAAAAGTGT	55298
rs398016602	in-del	-/AC	0	0	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997226	TCTTCTGCCTCACGT[-/AC]ACACACACACACACA	55298
rs398115493	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71945806	CAATAATAAAAAAAA[-/A]TAACCTAGTAAAAAA	55298
rs398115494	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71952818	TCTCAAAAAAAAAAA[-/A]TTTCATAAATACAAT	55298
rs527255189	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969107	GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	55298
rs527267676	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71976722	AGCAGCCCTGTTGGC[A/G]TATATTCCCTGGCAA	55298
rs527281749	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968872	TCCTCCTAGGATTTT[C/T]CTTTTTTCTTTCTTT	55298
rs527294602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962109	CATAGCTGGGACTAC[A/G]GGTGCCCACCATCAC	55298
rs527381827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932813	TGTCATCCCTGAGGG[A/G]ATCAAAATGAGGGTT	55298
rs527453198	in-del	-/T	0.192891	0.24339	intron-variant	RNF121	GRCh38.p7	11:71992838	TAAATATTTCTATTT[-/T]TTTTTTCAGAATGGA	55298
rs527467942	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956157	TGACGTTATCAGAAC[A/G]TGGGTAACAGGACCT	55298
rs527531189	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956710	TTTGCTCTAGCCATA[C/T]TCAATTGCTTGTGTA	55298
rs527540612	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948928	GACAGTTAGCCTGGT[A/T]GTGCTGAACCTACCA	55298
rs527543528	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939784	TTCAAAAGTCACTAT[A/G]TATTTATTGTGCACT	55298
rs527547255	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962885	TCACTCCGTTTTTTT[A/T]TAAATTTTATTTATT	55298
rs527548745	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939833	TTTTTAGTCTTGGGA[A/G]TTAATAAATGGACAA	55298
rs527634358	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985489	TCTCTCTTTTGTGAT[C/T]AGTGCAATCCCTGGA	55298
rs527693246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986155	TCTCCCTTCTCCCTC[A/G]GAAGAAAATTCATTT	55298
rs527695308	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977989	TTAGCCATTTATATG[A/C]CTTCCTTAATGAAGT	55298
rs527744071	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949489	GGAGGCCCAGGCAGG[C/G]AGATCACTTGAGGTC	55298
rs527763285	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998014	CTAGGGATCACCCTT[C/G]CTTTTACTTTTTCCC	55298
rs527776433	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71962818	TCCATTCTGTCCTAA[C/T]GTGGGTTGGGTTTTC	55298
rs527781587	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991034	TGGATATTCATGGAC[A/G]TAAAGATGGCAACAG	55298
rs527810739	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71941627	GAAGAGAAAGGCTAC[C/T]TTAAATAGGGTGATT	55298
rs527825116	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991976	AAAAAAAACCTAGCC[A/G]GGCGTGGTGGCACAT	55298
rs527877314	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71972060	AGTTAAAAGCAATAC[A/T]TTAAGTACCTGTAGG	55298
rs527891347	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964603	CCACCTCAGACTTCC[A/G]AGTAGCTGGGACTAC	55298
rs527987482	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71988216	AGATCTTTATTAGCT[C/T]ACAGGTCCTCCCACC	55298
rs527988732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935413	TCAGTGCTTGTGCTG[C/T]TAACCACAACGGGCA	55298
rs528008281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978592	CCATAATAAGAGCTC[C/T]CATTTACTGAGCGCT	55298
rs528120120	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937693	CTTTTTAGTCCTTGT[C/T]GTACCTTTTCCCAGA	55298
rs528130557	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71930839	GAAAATAACATTTTC[C/T]TTTTTTATTTGAGAT	55298
rs528137196	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952490	TATTTGTGTAAGTTT[A/G]TGGGATACAGACTGA	55298
rs528149330	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944318	TGCCTGGGCAACAGA[A/G]CGAGACTCTGTCTCA	55298
rs528298663	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967357	TTTTTTTGTTTTTTT[G/T]TTTTTTTTTTGAGAC	55298
rs528368721	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981630	CTGTCTTAGAGTTAG[A/G]ATTGTTTTATGCCTT	55298
rs528384631	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938477	GGCATGTGCCCCCAC[A/G]CCTGGCTAATTTTGC	55298
rs528397023	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931019	TTGTATTTTTAGTAG[A/C]GACAGGGTTTTTCCA	55298
rs528401066	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981840	AAGTGGGAATATGGC[C/T]CAGTCACTACCCACA	55298
rs528404732	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71956932	AAATTTTCTGTTTAC[C/G]TCTGTCTTTCTCACT	55298
rs528413283	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71974199	ACCCTCCTCGGCCTC[C/G]CAAAGTGCTGGGATT	55298
rs528472563	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953471	TGCTGGGATGTAGTA[G/T]CAGTGCTTCTCAAAC	55298
rs528560480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960664	TGTGTTCTGAGCTAT[A/G]TACTGGTGGGATATC	55298
rs528646477	snp	C/G	0.000133056	0.00815539	intron-variant	RNF121	GRCh38.p7	11:71990576	GGGTGGGTCTTTCTA[C/G]CTCTAATGCTTCCCT	55298
rs528647411	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976220	TGGCCTGCTGTCTTA[C/T]GGCCATGCTTATTTG	55298
rs528696748	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939933	TATAGTATGAGGAGT[A/G]GAGTTATAAATTACG	55298
rs528704024	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71950315	TATAGCCAGGCACGG[C/T]GGCTCACGCCTGTAA	55298
rs528742436	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963742	GGATAGCCAGTTGTC[C/T]CAGCATCATTTATTG	55298
rs528743157	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946863	GATTACAGGTGCTCT[A/G]GCTCTTTTTTTTTTT	55298
rs528782673	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939355	AATGGAATGGCTTAC[A/G]TGGCTTCTATAAAGT	55298
rs528789761	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71952774	CATCGTGCCACTGCA[C/T]TCTAGCTGGGGCGAT	55298
rs528805882	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947735	AAGTCATCAAAGTTT[G/T]TCAAAGTAGTAGGAT	55298
rs528832848	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990151	GATTCTGGCATGCCC[C/T]TTCCTCCTTATGGAT	55298
rs528970471	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971883	GCTGAGTCAGCGAAT[A/G]TACACATACCCTGTG	55298
rs529054184	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986353	TCTTCTGAGCATAGT[G/T]GTGTTTAATACTTTT	55298
rs529074832	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71982017	GTCTTGGATGTGATA[C/T]TGTCAGGCAGAAAGG	55298
rs529081994	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943378	GGGAGAGGTTTGGAC[A/C/G]TTGTTCTGGGACTCT	55298
rs529163147	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71959359	CTTACCACCTGGGTT[C/T]TACACTTTTTGTTAT	55298
rs529166003	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71942890	AAAGTTCTAGCAGAT[A/C]TGATGTCTGGCAAAG	55298
rs529179090	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950563	CACTCCAGTCTGGGC[A/G]ACACGACAGAGCAAG	55298
rs529261065	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980554	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTTAAA	55298
rs529337070	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936341	AGATTCCCATTTGAA[A/T]TCCCATTCCAATACC	55298
rs529416037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979547	TCAAGCCCAAAAACT[A/G]CAAAACAAAGCAAGA	55298
rs529507584	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71966115	ACCTCTGCCTCCCAG[A/G]TTCAAGTGATTCTCC	55298
rs529525249	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71960361	AGCGTATGAGACTTT[A/T]TGTCTATAACCTCTT	55298
rs529561996	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71956771	TAGTCCCTTTGCCTG[A/G]AATGTATTTCTCTTA	55298
rs529638814	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975501	CAGCCTTCCTTGGAG[C/G]GGGGTGGGTTCTCCA	55298
rs529642839	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976331	CCTGCTGCCCCCTCC[A/G]TTCTGGGTATATTCT	55298
rs529659796	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932639	GAAGCTGAGGTTCAG[A/G]GGATTTGAGATAGGC	55298
rs529702646	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976223	CCTGCTGTCTTATGG[C/T]CATGCTTATTTGTTA	55298
rs529730798	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71978850	AGAGTTAAACGATCT[G/T]CCTAAGTTAACGCAG	55298
rs529732439	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939254	TTTAAGCATGTGCAG[C/G]AAAAATTCAGTCTTT	55298
rs529758543	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931648	CGAGTGAAGAGACAT[A/G]CAAATAGCGTATTAT	55298
rs529777410	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953144	GCTTAAGCAGTCCTC[C/T]TGCCTTAGCCTCCCA	55298
rs529785581	snp	G/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71982637	ACTAGTGGAGTTAAC[G/T]TTATCCAAAGTTGTA	55298
rs529887026	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962811	ACAATTTTCCATTCT[C/G]TCCTAACGTGGGTTG	55298
rs529926967	in-del	-/TT	0.381962	0.212334	intron-variant	RNF121	GRCh38.p7	11:71980351	CCTGTAAAATGACAC[-/TT]TTTTTTTTTTAAGAT	55298
rs530042033	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71991681	GGAAAGAGCATTCAT[-/A]AAGAGTCCTGTCACG	55298
rs530142965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940944	GCAAAATGAAAAGAT[A/G]TGCAAGGCTTGGAGA	55298
rs530190393	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71983991	GGCTTTGGTAGTTTA[C/G]TTTAAAGGCCACTGT	55298
rs530232982	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948860	AACCTTTGGACTTCA[C/T]TTGTTATCTTAATCA	55298
rs530305088	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977872	GGCTTTCATGCTTTC[C/T]ACAGCATCAGGCACA	55298
rs530352792	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71977031	TCATTTATGAAAATA[C/T]TGAGCAGAGCCATGG	55298
rs530352941	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71935995	TGGGACTACAGGTGT[C/G]TGCCACCACGCCCGG	55298
rs530383898	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71993909	GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT	55298
rs530435695	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981502	TATGTATTATTTGCT[A/G]TCTTTTTTTATACCT	55298
rs530435782	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953424	CAAGTGTACAGATGC[A/G/T]TATGGCTGTAGATGC	55298
rs530441800	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71964148	CAGTACCTGAACACA[G/T]GATATCTTTTCATTT	55298
rs530444044	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71994487	CATCTAACTTCCCAA[C/T]TGTCTCTAGTCTGGT	55298
rs530453632	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944077	TAACTCATGTCTGTA[A/G]TCCCAGCACTTTGGG	55298
rs530455842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958417	CTTTGTTGTTATGGA[A/G]TATCGGATTAGGTCT	55298
rs530548680	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987585	TTTTACTGGAACATA[A/G]TCATGCCCATTCATT	55298
rs530550142	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944225	GTAATCCCAGCCACT[C/T]GGGAGACTGAGGCAG	55298
rs530574646	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71951111	TGCCTGTAATCTCAA[C/T]TACTCGGGACGCTGA	55298
rs530586165	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930359	ATTGAAGATGAGGTT[C/T]AGAGAAAGGGAGAAG	55298
rs530639267	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951633	TATAGCAAGACCCTG[A/T]CTCTTAAAAAAAAAA	55298
rs530736538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974155	ACCGTGTTAGCCAAG[A/G]TGGTCTCAATCTCCT	55298
rs530746395	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988134	AACGCTGCTCTGTTG[C/T]TTCCTAAGGGTGCAT	55298
rs530819107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945014	TTTTTTTTTTGAGAC[A/G]GGGTCTTCTGTCACC	55298
rs530839362	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929877	TGGCACTGAGAAGTG[C/T]GCAACATTTCAGCTT	55298
rs530870500	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980764	CATCAGTCCCATGTG[A/G]CTGCTGACTACTTGA	55298
rs530999285	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966674	TTTTAATTTTTTGTA[C/G]AGTTGGCTCTCACTA	55298
rs530999601	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974534	ACCAAGGTACAGAAT[C/T]CTGAAGTGATTTGCT	55298
rs531039191	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946697	TAAAATAAGATGGTT[A/G]CATCTTATTTTATTT	55298
rs531039493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938599	GCTGGGATTACAGGC[A/G]TAAGTCACTGCTCCC	55298
rs531065179	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71953420	GAGTCAAGTGTACAG[A/G]TGCGTATGGCTGTAG	55298
rs531086966	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989276	AGTAAGGATGGGGTT[C/T]CACCATGCTGGCGAG	55298
rs531124567	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946071	AGTTATGTTTGTGCC[A/G]CTGCACTCCAGCCTG	55298
rs531140400	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71973616	ACATGGTAAAACCCC[A/G]TCTCTACTAATAATA	55298
rs531190768	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962917	TAGCTACTTTAGTGG[A/T]TGTAGATGTCATTGT	55298
rs531230815	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71975589	AAGCACTTAATTGTG[A/G]TTATTTGTTTCTCCT	55298
rs531252240	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954385	GCTAATGATCCTCTA[A/G]GCCTCAAGTCTAGTC	55298
rs531268187	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71949714	CAAAACACATGCACA[C/T]GGCCGGGCACGGTGG	55298
rs531274231	snp	A/G	0.000149265	0.00863772	missense, intron-variant	RNF121	GRCh38.p7	11:71995441	TTTCCCTTGACCAGC[A/G]GTGCTCAGCTTCCAC	55298
rs531278702	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969822	TCCTCCCACCTTGGC[C/T]TCTCAAAGTATTGGG	55298
rs531314695	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970619	GTAAACTATGATCAC[C/G]TCACTGCACTCCAGC	55298
rs531316349	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927299	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	55298
rs531322432	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71990484	GTTTGCCCGCACTTG[C/G]TCTAGCCTTTGGGCC	55298
rs531353613	in-del	-/T	0.148661	0.22854	intron-variant	RNF121	GRCh38.p7	11:71993842	CTTTGACACTTCCTC[-/T]TTTTTTTTTTTTTTT	55298
rs531406616	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977830	TTCATGTGTTTATAT[C/T]GCATTAGCCAAGTCC	55298
rs531420259	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936546	AGGTGCCTGCCACCA[C/T]GCCTGGCTACTTTTT	55298
rs531432778	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950313	GATATAGCCAGGCAC[A/G]GTGGCTCACGCCTGT	55298
rs531519793	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949631	TAAGGCAGAAGAATC[A/G]CTTGAACCCAGGAGA	55298
rs531526301	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957375	GGAGGCAGTGGCTCA[C/T]GACCGGTAGGACTGG	55298
rs531554677	snp	A/G	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71992597	CAGTGAAGTGAGGAC[A/G]TACTGTATTTGAGAA	55298
rs531596007	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978751	AAGTGCTTTCCATGC[C/T]TTAACTCATTTAACC	55298
rs531608484	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986784	CAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAAT	55298
rs531680679	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966888	TTTTTTTTTTGAGAC[A/G]GAATCTCACTCTGTC	55298
rs531697331	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	RNF121, LOC100133315	GRCh38.p7	11:71928388	GTGGACCTCGAGGAG[C/T]CACCGTTGCCTCGGA	55298
rs531854399	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972727	ATGTCCCCTGGGAAA[C/T]AAAATCATCCCTGAT	55298
rs531859031	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939948	AGAGTTATAAATTAC[A/G]TACAAGATGCCACAA	55298
rs531865396	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986261	CGGGCCCAGGTACAA[A/C]CAACCTGTAGCTCAT	55298
rs531909502	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929019	TGAGCAGCGGAAGCA[G/T]CTGGCTCGCGCGGGG	55298
rs531978585	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958236	AGGCAACCTGGATTA[A/G]TAGTCTTCATATCAT	55298
rs531989760	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974823	CCACAAACTCAGTGA[A/G]TGATGATTGGTAGGC	55298
rs532130458	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989932	GGTCTTATGGGACAA[C/T]AGGCCAAATCTAGGA	55298
rs532143712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989192	GTCAAATGATTCTCC[C/T]GCCTCAGCCTCCTGA	55298
rs532189658	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71936122	AGAGTGCTGGGATTA[C/T]AGGCGTGAGATTATA	55298
rs532190468	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968142	TCTCGGCTCACTGCA[A/G]CCTCTGCCCCCGGTT	55298
rs532245126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975435	ATGATGCCTTTTTCT[A/G]TCTGGACCTATTGGC	55298
rs532251023	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961188	GGAACTATTCAATTG[G/T]AGAGAGCAAAGATGA	55298
rs532364485	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996713	AAGGCCTCAGCCCAC[C/T]CACTCCCTTCTTCCC	55298
rs532376810	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71940441	CGGCCTTCATGGATG[A/T]TTTGAATTTCATTAG	55298
rs532395085	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997198	AAAGCCTAAGAGTGC[A/G]TATGCGTGTGTGTGT	55298
rs532396311	in-del	-/AGAAT	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71979615	GTCTTTGTCCAACTC[-/AGAAT]AGAATCCAGGATCTC	55298
rs532404411	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967448	TCTGCCTTCTGGGTT[C/G]AAGCGATTCTTCTGC	55298
rs532410730	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968457	CTATCCTGGTTCTTA[C/T]AAAGTTCTTCTGCCT	55298
rs532456789	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980409	TGGAGTGCGATGGCG[C/T]GATCTCAGCTTGCCG	55298
rs532466268	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71943161	AGACGATGGAGAAAA[G/T]TGGATAAATTTAGAA	55298
rs532596606	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947994	CTTAGGAGTTCATAG[A/C]GGATAGTTCTGTTCT	55298
rs532607384	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954680	TGTCAAAGAGAGGCA[C/T]CTTCATGCCTGGCCC	55298
rs532641050	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946154	AAAATCCGCACAGAA[A/C]CTTATACACAAATAT	55298
rs532670534	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71947050	CTTGTATTTTAAGTA[A/G]AGACGGGGTTTCACC	55298
rs532684308	snp	C/T	1.64942e-05	0.00287173	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996210	CTGGGAGAGGCCTCA[C/T]GTCATGTATGGGCAA	55298
rs532760734	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976917	ACTTTTTTCATTTTG[A/T]TCTTATTTCTTCTAT	55298
rs532876486	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71991258	AAAATTAGCCAGATC[C/T]CAGATGTACCCTATA	55298
rs532965958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993369	ATTAAGCAGTAACTC[A/G]TTACCCCTTCCCACA	55298
rs533004301	snp	C/T	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71950999	GGAGGCTGAGGTGGA[C/T]GGATCACCTGAGGTC	55298
rs533015873	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937005	ACTGGCATGCCTACT[A/C/G]TCTGTTCTGGAAATA	55298
rs533099297	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71944011	GATTTTTATCTGTAG[C/G]TGATGATTAGCTGTA	55298
rs533165009	snp	A/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71974130	GTATTTTTAGTAGAG[A/T]CGGGGTTTCACCGTG	55298
rs533177538	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980619	CCCAAAGTGCTGGGA[G/T]TACAGGTGTGAGTCA	55298
rs533178949	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966584	ACACCTGGGCCCAGG[A/C]AATCCTCCTGCCTCA	55298
rs533248177	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71985106	TTTAATTTTTATTTT[C/T]AGTAGAGACAAGGTC	55298
rs533299668	snp	A/T	1.65141e-05	0.00287346	intron-variant	RNF121	GRCh38.p7	11:71986974	CAGAATCTCTGTGTC[A/T]GCTGCACTAACCTTC	55298
rs533301364	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937375	GCCCAGGCTGGAGTG[C/T]GACCTTGGCTCACTG	55298
rs533329177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960475	GCTACAGGAAAGGTG[C/T]CAGCTGTTTCTTCCA	55298
rs533331389	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952667	TACAAAAATTAGCCA[A/G]GCGTGGTGGCGCATG	55298
rs533393614	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71953247	CTGTGTTACCCAGGC[C/T]GGTCTCAAATTCCTG	55298
rs533536564	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961317	TGTAATCCTAGTACT[G/T]TGGGAGATTGAGGTG	55298
rs533551882	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954968	AGTGCTTAATATATG[C/T]TCAGCTCTGTGCTGT	55298
rs533597434	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988509	TATTTTAGGACAAGT[A/G]AAAATAAATCCTGGC	55298
rs533599232	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71930486	GAGAAATTGACAGGT[G/T]ATCACAGCAGGGGGA	55298
rs533618069	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945155	ACCACACTTGGCTAA[G/T]TTTTAAATTTTTTGT	55298
rs533700077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990848	CTTCAAGATGTGCAT[A/G]TGCATGGACATTCCT	55298
rs533700609	in-del	-/TTAC	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71931299	ATTCCAGGAACCTTG[-/TTAC]TTGTTTCATTTCCTG	55298
rs533759428	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984167	AGATGATATGAAGAA[A/G]AAGTGCAATAGAACA	55298
rs533809289	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955554	GGGTTCTTAAAGGAT[A/G]ACTAGGATGTAGATA	55298
rs533818424	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947288	CAGCGCCGGAGGATC[A/G]CTTGAGCCCAGAAGT	55298
rs533830383	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996418	GAAAGACTCAAAGGG[G/T]TGCTTGGGCCACTCA	55298
rs533882429	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990378	GAGGGGATACTGTAG[C/T]TTGGTCTTCACAGCC	55298
rs533912959	snp	A/C			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927589	ACTATATAGTCATGG[A/C]TACATATAATTATTA	55298
rs533935343	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71969260	TACTCACGTAAAGGT[A/G]AATGGGTGAGTTAGT	55298
rs533972172	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948279	CCAGCACTTTGAGAG[A/G]CCGAGGCAGTTGGAT	55298
rs534039182	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940377	AGGGGAAGTACCCTC[G/T]CATGGATATGGCTAG	55298
rs534066160	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976536	AATTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT	55298
rs534068461	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984702	TCCTGGCTTAGCCTC[C/T]CAAGTAGCTGGGACT	55298
rs534151697	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71977145	TCTCTACCTTTATTC[C/T]ACTACTTGGGCTTAT	55298
rs534168739	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986506	GGTGTGGTGGCTCAC[A/G/T]CCTATAATCCAAACA	55298
rs534202742	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71959946	CGGCCTCTAATTCCT[C/T]TCTCATTCCTCTCCT	55298
rs534215443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970220	GCTAGGGAGTAGGGG[A/G]AATTAGGGCCTATAG	55298
rs534215952	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926802	GCTACTGAGGAGGCT[A/G]AGGCAGGAGAATCAC	55298
rs534242633	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933000	ATGATGACTGCCTAA[A/G]CTCAGTTCTGTCTCT	55298
rs534278663	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71980875	AATAATTTTAATCTT[G/T]AATACATATTGAGAT	55298
rs534279605	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71932475	ACTATTTGTGCTCTA[C/G]GGGGTGGGAACTTTA	55298
rs534312896	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933653	ACTTCATGTTCCCTC[A/C]GCCCGCTTGTACTTT	55298
rs534339764	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71973711	AGTATTGCCTGAACC[C/T]GGGCAGTGGAGGTTG	55298
rs534389502	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987208	TATTAACAGGAGGGA[C/T]GTAATATCCAGGATA	55298
rs534390871	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71953294	TGCCTCAGACTCCCA[A/G]AGTGCTGGGATTACA	55298
rs534400516	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957085	TCAGTGTGAAATAGA[A/G]TGGTTGGTAAGGCTT	55298
rs534424382	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71993601	TATTCATTCATCTGT[A/G]GATAGGCACTTGAGT	55298
rs534485395	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976771	CCCTAAGCCTGTTTC[A/G]TGTGAGCTACTATTA	55298
rs534564953	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973100	CTGAGGCAGGAGAAT[C/T]GCTTGAATCCAAGAG	55298
rs534665251	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71936584	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	55298
rs534694454	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945427	CTGGATTCTTCTGCA[A/G]TATCATCCCCACTGT	55298
rs534739390	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929416	CTAGCTGGGTGTCTT[A/G]GGGTAGGACCGAAGG	55298
rs534744895	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938269	TTTTTAGTGCGTACT[A/G]TGTGCCAGGCAGTAA	55298
rs534757959	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71980307	CTTTTCTCTGTTCTG[C/T]TCTGTTCTCTTCTCA	55298
rs534801338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959419	CTGGGTTATTTTTGC[C/T]GTTAATGTTTAATTG	55298
rs534810067	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991383	TCTAGACACATAGCT[A/G]TATGCCAGAATTACA	55298
rs534814510	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960041	AGCCAAGGGAATCAC[C/T]TGCTGCCAGTCTTTA	55298
rs534822096	in-del	-/TCTGT			intron-variant	RNF121	GRCh38.p7	11:71980297	CTGCTTACCCTTTTC[-/TCTGT]TCTGTTCTGTTCTGT	55298
rs534824535	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952143	CTTTGGCAATACAAA[C/T]GAATGAACTACAGTA	55298
rs534859125	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975113	TTCCCTCCTGGAACC[A/G]GTGAGTGGCAAAATC	55298
rs534924898	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967653	GTCTCGATCTCCTGA[C/T]CTCGTGATCTGCCCA	55298
rs534947607	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938816	TATAGGTTAATTTGG[G/T]TTTGAGCTCTGTAAA	55298
rs535200338	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71947368	GTGGCATGTGCCTAT[A/G]GTCCTAGCTACTCAG	55298
rs535239574	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975735	CGTTTGCTTGAAGTG[C/G]AAAAGATGGGAAAGA	55298
rs535254013	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71995128	GTCACAGGGGAAGAG[A/G]ACCCTCTAATGGGAT	55298
rs535268787	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71954733	TCCCCCTCATTGGAT[A/T]TGGTTTCTTGAACAG	55298
rs535301432	snp	A/C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927300	GCACTTTGGGAGGCC[A/C/G]AGGCGGGTGGATCAC	55298
rs535303762	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978816	CATTTTACCATAGTT[C/T]AGAGAACTGAAGCTT	55298
rs535316639	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942175	CCTGACCTAATAATC[C/G]ATCTGCCTCGACCTC	55298
rs535367562	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984878	AAGTGTGAGCCACCA[C/T]GCCCAGCCCTGTAAC	55298
rs535381445	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71982209	CACGTGGTGGCACGC[A/G]CCTGTAATCCCAGCT	55298
rs535509347	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956427	GGACGCTATGGCAAT[A/G]TACAGGACACCTTCC	55298
rs535615876	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993567	TAGTATTCCATTGTG[C/T]GTGACACCGCATTTG	55298
rs535659087	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951142	GGTGGGAGAATCGCT[G/T]GAACCTGGGAGGCAG	55298
rs535669345	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927682	GAGGGTAATAGGCTT[A/G]AGAGTAGAAAAAACA	55298
rs535762950	snp	A/G	0.00486615	0.0490856	intron-variant	RNF121	GRCh38.p7	11:71978055	CTAAAGTAGAAACTG[A/G]AAAAAATTTTTTGTA	55298
rs535852036	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957731	TACAGGATGGGGAGC[C/T]CTGGTTAAGAAAATG	55298
rs535870574	snp	G/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71948019	TGTTCTGAAAGATTC[G/T]GGAGGAGGTGACACC	55298
rs535881615	snp	A/G	1.66693e-05	0.00288693	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960760	TTCAGGGTCGAGCAC[A/G]CACGCATGCATGCCA	55298
rs535900926	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71977509	CTGTTAGCATCTAAC[A/T]TCGTCATCTCAACTG	55298
rs535977283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974970	CTTCAGGGATGTTAG[A/G]GGAAGGGATAAGTTT	55298
rs536105081	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943621	CTTGCTCTCAGGTTG[A/C]TCATGGTGTAGTGGA	55298
rs536423133	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954878	TTTAAGCATCTCCAG[A/G]TGAGGTGCTGGTTTG	55298
rs536450618	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71967151	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	55298
rs536458308	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955726	TTGGAGAAGAAGAAG[A/G]AGAGTTTTGGCATGT	55298
rs536488766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947158	CTTGAGCCACTGTGC[C/T]TGGCTGGTTGCATCT	55298
rs536533636	in-del	-/G	0.0166325	0.0896639	intron-variant	RNF121	GRCh38.p7	11:71986786	AAAAAAAAAAAAAAA[-/G]AAAGAAAAAAAATAC	55298
rs536600581	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984125	CCTAAAAATGGGACA[A/G]TAATTGCTACCTCAC	55298
rs536601275	snp	C/T	1.64879e-05	0.00287118	intron-variant	RNF121	GRCh38.p7	11:71987121	ATTCAAGTGAGTACC[C/T]TTTGTTTTTGTTTTT	55298
rs536665257	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71976504	GGGACTGCAGGTGTG[C/T]GCCACTATGCCCAGC	55298
rs536678794	snp	C/G	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71936510	TTCTCCTGCCTCAGC[C/G]TCCCGAGTAGCTGGG	55298
rs536756766	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940233	AGAAAACCATGTTTC[C/T]TGCATTCAGGGAATT	55298
rs536794972	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993507	AGCGTAGTGTTTTCA[C/G]AGTTCATCCATGTAT	55298
rs536830331	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962391	GAAAAACTCAATCTG[A/G]GAAACAGTTAAGAGG	55298
rs536970978	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969172	GATTACAGACGTGAG[A/C]CACCGTGCCTGGCCC	55298
rs537027781	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71952082	ATGCCTACATTCATC[A/G]GCTGATGAATGGATA	55298
rs537087571	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944631	AGCTCACTGTCCGTG[C/T]TCCTGTGGAGGGCAT	55298
rs537097800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943047	AATCACCTCCTAAAG[A/G]TTCCCTCCACCTCTT	55298
rs537133865	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992946	CCTGTCTCAGTGTCA[C/T]CCCCCAAGACCCCAC	55298
rs537197152	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986568	GTCAGGAATTCGAGA[C/G]CAGCCTGGCCAATAT	55298
rs537201158	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71981582	AGGGAGTTAGGAGGC[A/G]TTGGAGAGAAGACTA	55298
rs537251337	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71965700	AGCAGTTTTATAGAA[G/T]GCACTCCTAGAAATG	55298
rs537298812	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945371	GAGTCACTTTTAAAC[G/T]TAGTAGCCGTTGGCT	55298
rs537377515	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71973043	AATACACTGTTAGCC[A/G]GACATGGTGGTGCAT	55298
rs537396704	in-del	-/TC	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71985035	CAACCAATTTTCCCA[-/TC]TCAGTCTCTGTAGTA	55298
rs537408857	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71994136	TCAGCCACCGCGCCC[A/G]GCCTCCTCTTATTTC	55298
rs537428204	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955676	ACGTGTCTTGGGACA[A/G]TTAATAGATAGGCTT	55298
rs537490505	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956393	AGTATTATTCTAGAG[C/T]AGTGGTTTTCAACTA	55298
rs537527389	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71976590	GTCTCGATCTCTTGA[C/T]CTCGTGATCTGCCTG	55298
rs537669019	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71985500	TGATCAGTGCAATCC[A/C]TGGAGAATAGAGCTG	55298
rs537673699	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981998	TAGACGGAAGGCTTC[C/G]TGTGTCTTGGATGTG	55298
rs537674470	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71977228	ATCCCTAGCTTACAA[C/T]ATGAGGGGATGCAGA	55298
rs537692357	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932946	GTTAGGGAGAGGAGA[C/G]ATGGGCCTAGCCAGC	55298
rs537700614	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937376	CCCAGGCTGGAGTGC[A/G]ACCTTGGCTCACTGC	55298
rs537719714	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994935	GAGGGTGGTCATGAC[C/G]CTAGGCATGCTGTCC	55298
rs537729320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987830	GAGTGGTGTCTGCAA[A/G]TCTTCACAGTAGACT	55298
rs537732542	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990952	GAGGCCTTTATCATA[A/T]GCCAGTTAATGCAGG	55298
rs537798071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984315	GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG	55298
rs537917524	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962260	TGAGCCACCGCGCCC[A/G]GCAGATTTTTACAAC	55298
rs537924933	in-del	-/TAAG	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71967817	CATTGTTTACATTAT[-/TAAG]TATTATATGTAAGTA	55298
rs537987939	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940825	CTCTGCTTCGGGAAT[C/T]CTTAAAGACTTAATG	55298
rs538020322	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71992308	CCACTGTCACTTACT[C/G]CTTTACCAAAAATTG	55298
rs538073319	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933904	TCTGCCTAATGGTAT[A/G]TGCTTTTTTATTAAA	55298
rs538089057	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71986708	CAGGAGGTGGAGGTT[A/G]CAGTGAGCTGAGATT	55298
rs538111710	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977858	TCCTGGAGGGCCAAG[A/G]CTTTCATGCTTTCCA	55298
rs538125789	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71988857	AAATCCTATTTTATA[C/T]AGTGAGAGTGCACTC	55298
rs538136036	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71960240	AGTCTTAAGGATTTC[A/T]GACTCTGGCAGAGAG	55298
rs538158968	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940992	TATTCTGGGACTGTA[C/T]GCAGTTCTGTATGAC	55298
rs538184207	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991513	ACAACTTTAATAAGC[A/G]TTATGTAGGAAAGGT	55298
rs538248016	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964057	ACAAACAAAATCAGT[A/T]GGAATTTTGATAAAG	55298
rs538264049	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966919	ACCCAGGCCGGACTG[C/T]GGACTGCAGAGGCGC	55298
rs538332233	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926870	CACCCCTCTGTACTC[C/T]AGCCTGGGTGACAAA	55298
rs538344613	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927657	TAATAGTTGCTTCTG[C/G]AGAGGATGAGAGGGT	55298
rs538377936	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973752	AGATCCTGCCACTGC[A/T]CTCTAGCCTGGGTGA	55298
rs538472609	in-del	-/AGAATAT	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71956371	GAGCCCTAAACTCAA[-/AGAATAT]AGTATTATTCTAGAG	55298
rs538482854	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950552	TCATGCCATCGCACT[C/G]CAGTCTGGGCGACAC	55298
rs538489317	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71964396	TAATAGTTTTTAAAG[-/T]TTTTTTTTAGGATTT	55298
rs538596430	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967991	TAATTTGCTACGGAT[A/G]TCTTTCCCCAGTTTG	55298
rs538599229	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71962315	ATATATGCACTGCAG[C/T]AATTTTCAATAAGAA	55298
rs538617863	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71938764	ACAATTTTTTCCTTT[A/T]TGGTAGGATCATCTC	55298
rs538695794	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930025	ACCTATCTAATAGGC[A/G]TTTAAAGACTGGTGT	55298
rs538729829	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944628	AAGAGCTCACTGTCC[A/G]TGCTCCTGTGGAGGG	55298
rs538774236	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938974	CAATGGTGTGATCTC[A/G]GCTCACTGCAACCTT	55298
rs538800785	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989628	GTACAAATATTTTAA[C/G]AGATAATTTTCTATA	55298
rs538808702	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930058	TAAAATACCAGTGGT[C/G]CTTGAAGGAATCACT	55298
rs538817183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952935	TCAGCAATTTTGAAA[C/T]GTACAATATTCTGTT	55298
rs538853105	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968290	ATCTCGAACTCTGGA[C/T]TTCAAGTGATCAAAC	55298
rs538879410	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953790	CCTACAGATGCAGAG[A/G]TCATAGGGTTTATGA	55298
rs538889856	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963345	TTCATAGTCTTGGCC[C/T]GGTGGGGTGGCTCAA	55298
rs538908113	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996527	TTTAAAAGAAAACTA[C/T]TTTGATGAATATATT	55298
rs538929137	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71965951	ATTAGTGAAGTTGAG[A/C]ATGTTTTCATGCTTA	55298
rs539022899	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992818	GCCAATCTGAGAAAC[A/G]CAAGTAAATATTTCT	55298
rs539052774	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71939417	ATTTGCACCGCCCCC[C/T]GCAACTTCCCTCCAC	55298
rs539059839	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975296	CAAAAACTTGTAGCT[C/G]TGGTATCTTTATCAG	55298
rs539091062	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946279	TGGAATATTATTTAG[C/T]AAGAAAAGGAGTGAA	55298
rs539092613	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934879	GAAAAGAGTGCTGAG[A/G]GTGAAATAATACAGA	55298
rs539179920	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71989453	TGAACTCTACAATGA[C/G]GAAAACAGAATTGAG	55298
rs539230153	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968987	GCCTCTTGGGTTCAA[A/G]TGATTCTCCTGCCTC	55298
rs539265690	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973003	ACCATCCTGACCAAC[A/G]TGGAGAAACCTTGTC	55298
rs539305452	snp	A/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71935909	CTAGAGTGCAGTGGC[A/G]TGACCTTGGCTCACT	55298
rs539310385	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931869	TCTGTTTTATTGATA[G/T]ACTCTAATGTGGAGC	55298
rs539359188	in-del	-/AC	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71970826	CCAAGACAGGGACTT[-/AC]CTTGCCTTAAGACAC	55298
rs539372655	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928645	CGTGGAGGGAGCGGA[A/C]TTTAAACTTCCGGGT	55298
rs539373262	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975815	GTTTACTTTGTGCTC[C/T]TCTGAAAGATAAGAG	55298
rs539397364	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71985909	ACCAGTCTGGGCAAC[A/G]TTGCAAGACCCCATC	55298
rs539429773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958514	CAAGGTATATTGAGA[A/G]GTAATGAGCTTTCTG	55298
rs539490061	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949962	GCCAAGATTGCGCCA[A/G]TGCACTCCAGTCTGG	55298
rs539570224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992274	TCCTTGATTTAACCC[A/G]CAGCCGCTACAACAA	55298
rs539612473	snp	A/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929724	TTCATGCATTTATTC[A/T]CTTAATAAACATTAT	55298
rs539719796	snp	G/T			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996883	TCTCCCCCTGTCCAA[G/T]AGCTATAGGCTGGTT	55298
rs539776556	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978862	TCTGCCTAAGTTAAC[A/G]CAGTAATTAGCTGTA	55298
rs539794077	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71994087	CCTCGTGATCCGCCC[G/T]CCTTGGCCTCCCAAA	55298
rs539801067	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980759	GTAGCCATCAGTCCC[A/G]TGTGGCTGCTGACTA	55298
rs539816676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989138	CGCCTAGGCTAGAGT[A/G]CAGTGGCTCACTGCA	55298
rs539837690	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71936004	AGGTGTGTGCCACCA[C/T]GCCCGGCTACTTTTT	55298
rs539837839	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954227	ACAGGTTAATTATAG[A/C]CATAGTTTACTCCTT	55298
rs539842700	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945902	TGGATCACTTGAACC[C/T]GGGAGTTCAAGACCA	55298
rs539923276	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71957456	GTAAGCAGATGATTG[C/T]ACCAAATCATCTATC	55298
rs539964064	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995362	AGAGCTGATAAAGAG[C/G]GAAGGCAGGATTTGA	55298
rs539986003	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71953165	TAGCCTCCCAAGTAG[C/G]TGGGACTACAGGCAC	55298
rs540007323	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71936668	CAAAGTGCTGAGATT[A/T]CAGGCGTGAGCCACT	55298
rs540012524	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975425	AACACCCATCATGAT[A/G]CCTTTTTCTATCTGG	55298
rs540073359	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968065	ATTAGATTTATGAAC[A/G]ATCTTTTTTTTTTTA	55298
rs540096692	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71943735	CAGAAAAGACTCCCT[A/G]GAAGTGATACCATAG	55298
rs540121394	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989797	AGATTATTTATATTT[G/T]TAGTTTATAATTTTA	55298
rs540181813	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71984790	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	55298
rs540181981	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982532	TAGCAAGAGCTCAAA[C/T]GGAAAGGAAAGAATA	55298
rs540191532	in-del	-/AAAA/AAAAA/AAAAAA	0.391397	0.206172	intron-variant	RNF121	GRCh38.p7	11:71982335	GCAAGACTCCATCTC[-/AAAA/AAAAA/AAAAAA]AAAAAAAAAAAAAAA	55298
rs540197714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995864	GGAGGCCCTCCCTGC[A/G]TGTTAGTCATGGGGA	55298
rs540242115	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938479	CATGTGCCCCCACGC[C/G]TGGCTAATTTTGCAT	55298
rs540262679	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71961451	CTATAGTCTCAGCTA[C/T]TGGGGAGGCTGAGAG	55298
rs540308829	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71978985	GGACTTCTAGAAATG[A/G]TCTGAAGGCTAACAG	55298
rs540411901	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931485	GGTATTCAGGTTTCT[A/G]CTAATGTCTCCCCAG	55298
rs540503024	snp	G/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71939078	CCCGGCTAATTGTTG[G/T]ATTTTTGTAGAGATG	55298
rs540539180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947757	TAGTAGGATGATGCA[A/G]TCAGGTGTGTGTCTA	55298
rs540596346	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927715	TAAGTTTAACTTTTA[C/T]TGTATTATCTAGCTT	55298
rs540637335	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955283	ATAACATGAGACTGA[A/G]TGACTAACATAGAAC	55298
rs540724596	snp	G/T	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71942938	GGGCTCCTTGTTGCT[G/T]TGTCTTCACATGGCA	55298
rs540727295	snp	A/G	0.00159617	0.0282053	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928907	GACCCTGAAACGTGC[A/G]GCAAGTAGATAACCT	55298
rs540796230	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991183	CACGCAGTATGCCCA[C/T]GTAACAAACCTGCAC	55298
rs540797314	in-del	-/C	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71942809	ATATATATGTACACA[-/C]ACACACACACACACA	55298
rs540813015	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972630	TATTATAGGATGTTT[A/G]ATAGCATCCCTACCC	55298
rs540848213	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71945203	ATGTTACCCAGCTGG[G/T]TCTCCCAACTCCTGG	55298
rs540937698	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71988171	GGATGGAATTTTGGC[C/T]GTTGCTTCAGTTGTC	55298
rs540959344	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955869	AAGGCCTGAGTCAGG[A/G]CACCTGAATAAATTC	55298
rs541013936	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937395	TTGGCTCACTGCAAC[C/T]TCCGCCTCCTGGGTT	55298
rs541033746	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981080	TTGAGATGGAGTCTT[A/G]CTCTGTCACCCAGGC	55298
rs541043205	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71965856	AGTGTTAAAGAAGGT[A/G]TAGGGTATAGTCAGT	55298
rs541045085	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71958060	GTTGTGTACCTCAGC[G/T]ACCAAAATATTCTGA	55298
rs541101109	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971987	GCAATCTGGATATCT[A/G]TCTCTGAGGGAGTAA	55298
rs541200674	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71993775	ACATGCCAAACTCTT[C/T]GCTTTCTTAATTATG	55298
rs541366923	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958719	CAAAAAAATAATATA[G/T]GTATATGTACCTACA	55298
rs541446360	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71932710	AACCCATGTTTCCAG[A/T]TTCCAGAGTGTTTGT	55298
rs541565077	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983642	TCATTCAAATAAGCA[C/G]CTACTGTGTGCCAGG	55298
rs541639303	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963509	CCTGTAATCCCAGCT[A/C]CTCGGAAGGCTGAGG	55298
rs541742448	snp	C/T	0.0138799	0.0821421	intron-variant	RNF121	GRCh38.p7	11:71938507	CATTTTTAGTAGAGA[C/T]GTGGTTTCTCCATGT	55298
rs541751478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974430	CCTCAGTAGACTTGA[A/G]TTCTTCTCATTTATT	55298
rs541763334	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969653	CTGCAGCCTCAACCT[C/G]CTGGGCTCTGTTGAT	55298
rs541777782	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984336	GGCTGGAGTGCAGTG[G/T]CACGATCTCGGCTCA	55298
rs541780858	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927209	CAGTTATCACGCCAC[C/T]GCACTCCAGCCTGGG	55298
rs541848965	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991772	CCTGGAGAAGTAGTG[A/C]CTAGACTAGAAAAAA	55298
rs541868980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950207	GGCCCTTTACAGTTA[A/G]CAGATACTTGAAGCC	55298
rs541907803	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71949206	GCGGGTCACTTGAGC[C/G]CAGAAGTTCAAGAGC	55298
rs541947967	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71987873	GTGAGGGAATGAGAT[A/G]ACACAGATGGGTGTG	55298
rs541983887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986643	GTGTGGTGGTGGGCA[C/T]CTGTGGTCCCAGCTA	55298
rs542044161	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983064	AAAACAAGCTGATTG[A/G]TAGAACCCCTCCCCT	55298
rs542197075	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71994129	ACAGGCGTCAGCCAC[C/T]GCGCCCAGCCTCCTC	55298
rs542205068	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949351	TAGGCCTGGAAAGTC[A/G]ACACTGCAGTGATCT	55298
rs542254435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941463	ATTTTTCTAGGTCCC[A/G]GTAATTCAGCAGTGA	55298
rs542255957	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71952401	TGGTGGTGATAGTGG[C/T]ACAACTTTGTGAATA	55298
rs542343416	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956636	GGCTACCATAGGGCC[A/T]TTTAGAGTCACATGG	55298
rs542364922	snp	G/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996938	ACTTGGCCAACAAGG[G/T]AAGCCTTGGGGCCTC	55298
rs542384325	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959824	TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT	55298
rs542407245	in-del	-/AG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929356	GTGAAGATGGAGGAC[-/AG]AGAGAGAGGTCGGAG	55298
rs542428083	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71935152	TGCTCAGACTGGTCT[C/T]GAACTCCTGGACTCA	55298
rs542491223	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936038	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	55298
rs542515746	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71942616	AAAAATATAAAAAAT[A/T]AGCTGGGCATGGTGG	55298
rs542521012	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71984123	TCCCTAAAAATGGGA[C/G]AATAATTGCTACCTC	55298
rs542533763	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71942885	AAGGCAAAGTTCTAG[A/C]AGATATGATGTCTGG	55298
rs542558610	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989123	GGAGTCTTGCTTTGT[C/T]GCCTAGGCTAGAGTG	55298
rs542595215	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960308	AGCACACATTTGCAG[C/T]GTTACTCCTTTACTG	55298
rs542655602	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945028	CAGGGTCTTCTGTCA[C/T]CCAGGCTGGAGTGCA	55298
rs542725512	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71994075	TCGATCTCCTGACCT[C/T]GTGATCCGCCCTCCT	55298
rs542784654	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71972367	GCCATTAGAGCTTTT[-/A]AAAAAAATGCCTCTT	55298
rs542829157	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938406	CTCACCATAACCTCC[A/G]CCTCCTGGGTTCAAG	55298
rs542917075	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945845	AGGCCAGGCCCAGTA[G/T]CTTACACCTGTAATC	55298
rs542987806	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954400	AGCCTCAAGTCTAGT[C/G]TCAGCCTTAGTTCTT	55298
rs542994847	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967833	AAGTATTATATGTAA[C/G]TATTATTCACAAGAT	55298
rs543059893	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968454	TTTCTATCCTGGTTC[G/T]TATAAAGTTCTTCTG	55298
rs543060932	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931398	TGTTTGAGAAAGTAA[A/G]CTCTGAGAAGCAGAA	55298
rs543083584	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71982458	GCACTCCTCAAAAGG[A/G]TGGACACTGAATGCA	55298
rs543120708	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974547	ATCCTGAAGTGATTT[G/T]CTGGGAACACATGAC	55298
rs543129503	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985992	TTTCTTGCTGAGTCT[A/G]GTAGCTGGGATCCAC	55298
rs543171853	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927982	CAGATCCAGGCGGAC[A/G]CCCAGAGGCGTGTGA	55298
rs543205011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955177	GTACCTGAGAGTGAG[C/T]GCTTCCTTAAATTTT	55298
rs543212014	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71950400	ACTGGCCTGGCCAAC[A/G]TGATGAAACCCTGTC	55298
rs543317095	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950476	GTAATCCCAGCTACT[A/G]GGGAGGCTGAGGCAG	55298
rs543323730	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71991912	GAGTTCAAGACCAGC[C/T]TGAGCACCATAGTGA	55298
rs543369376	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71961434	GGCGTGGTGGCATGC[A/G]CCTATAGTCTCAGCT	55298
rs543387221	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943837	GCATGTGCAAGGTGG[A/G]AGGTGAGAAAGAGAA	55298
rs543418824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964359	TTGTGTTAGTCTTCC[A/G]ACTTTGCTGAATTTA	55298
rs543419469	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987305	AAGGAATGTCTGAAT[A/G]TATACAAAGTCAGAG	55298
rs543465322	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972599	TAATTCTTTTTTTCT[C/T]GGGGGCTGTCCTGTA	55298
rs543475045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951314	ATTCATTGACATATA[A/G]CAAGTAAAGACCTGT	55298
rs543482255	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997010	AGCACCATGGATACT[C/T]GCCCGTGGGCAGGGC	55298
rs543529837	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71968265	GGGTTTCACCATGTT[C/G]GCCAGGCTGATCTCG	55298
rs543582706	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978335	ACCAGCAGCTGCTTT[A/C]TAGGCCCCAAGCAGA	55298
rs543621604	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71966428	CCCAACTCTGTCAGT[C/T]GCTGATTCTTCTGTG	55298
rs543687779	in-del	-/TTTTTTTTTTT	0.287867	0.247116	intron-variant	RNF121	GRCh38.p7	11:71938315	TGTGTAGTCTCTTAA[-/TTTTTTTTTTT]TTTTTTTTTTTTGAG	55298
rs543701648	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71945668	ATACAAAGAAGAATA[C/T]GACTCAAATGATCCT	55298
rs543709181	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929529	AGCCTAGGGTGGGGG[C/T]TGGGGACACAGACCG	55298
rs543737660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957380	CAGTGGCTCATGACC[A/G]GTAGGACTGGTCTTT	55298
rs543743518	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973235	TAGTGGCTCATGCCT[C/G]TAATTCCAGCATTTT	55298
rs543778443	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936141	CGTGAGATTATAGGC[A/G]TAAACTGCTGCGCCT	55298
rs543792466	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994265	GCCACAAATGTCTGA[A/G]AATGCCCTTGTCACC	55298
rs543902429	snp	A/G	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71986785	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAAAATA	55298
rs543909168	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71931616	TGAGTAAGACAGGAT[C/T]TTTACCAATTTACAG	55298
rs543940395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993726	GAATGGAATTGCTTG[A/G]TCATTTGGTAATTTT	55298
rs543958041	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71939333	TTACTGACTCCACAG[A/T]TGGAACAATGGAATG	55298
rs543976192	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989965	TCATGTAGGTACTTA[C/T]ATAACAAGAGAAAAA	55298
rs544026953	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969453	AGTTGACACTTTTTA[A/T]AGAAAGGTAAAAATA	55298
rs544101349	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961777	ATAGTAAATTCACTT[G/T]AGGTGGAAAGACACA	55298
rs544148182	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976152	GTGTCTTCAGTTGTT[C/G]CTTATGTGATTTGGT	55298
rs544238808	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939738	TAGTGTACACTATTG[C/G]TGGTATACACTATGA	55298
rs544240984	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71936967	TAAGGATAAAGGGAA[A/T]GTTGACTAAATTGCA	55298
rs544281560	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956598	AACTAAATTCAGTTT[G/T]CCCAGGTCCAGTGTA	55298
rs544316978	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71995996	CAGACAGGCTGTGAG[A/G]AGGAAGAGGAGGGGG	55298
rs544448409	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71988005	TGCCTGTAATATAGC[-/T]TGACATTCGACAAGA	55298
rs544480589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983482	ATAATTTTCCAATAA[A/G]CAATACTTCCTTCTT	55298
rs544538451	snp	C/G			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962190	AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT	55298
rs544571953	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991268	AGATCTCAGATGTAC[C/T]CTATAATTTTTCTCT	55298
rs544700095	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71980422	CGCGATCTCAGCTTG[C/G]CGCAACCTCCACCTC	55298
rs544795903	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941404	GGTCTGTATTAATTA[A/T]TCATTATTTCCTTCT	55298
rs544829577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934454	GTAAACCCCCAGTGG[A/G]CAGACTGTGGAAGTT	55298
rs544846980	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988117	TTAGTATTATCCCAG[A/G]TAACGCTGCTCTGTT	55298
rs544864863	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948211	GCTCCCAAATTTGAA[A/C]AGTTTAATTTAAAAA	55298
rs544874572	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930255	GATTGGTTGTCAGAG[A/G]TAGAACCAGTGAGAT	55298
rs544885315	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949329	AAACTGAGGTGGGAG[A/G]ATTGCTTAGGCCTGG	55298
rs544893219	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991728	TTTTTGAGGAACTAA[C/G]ACCATTGCGGTTGTA	55298
rs544954300	in-del	-/GTCA			intron-variant	RNF121	GRCh38.p7	11:71966422	CCCCTGCCCAACTCT[-/GTCA]GTCGCTGATTCTTCT	55298
rs544986699	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71939780	TATTTTCAAAAGTCA[C/T]TATGTATTTATTGTG	55298
rs545018238	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958743	ACCTACAATGTGCCA[G/T]ACACTGCTGGTTCTA	55298
rs545027144	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942736	GCCACTGCACTCCAG[C/T]GAGACTCTGTCTCCA	55298
rs545066726	in-del	-/C	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71942811	ATATATGTACACACA[-/C]ACACACACACACATA	55298
rs545115725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930817	CAGCAGAAGTTTTGG[C/T]AGAGGAGAAAATAAC	55298
rs545199601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954311	ACCTTTTTGGTCAGG[A/G]GGCAAATATTAAAGC	55298
rs545412359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960487	GTGTCAGCTGTTTCT[C/T]CCATGGGGGCAGGCA	55298
rs545437193	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71981509	TATTTGCTATCTTTT[G/T]TTATACCTGCTACTC	55298
rs545438592	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938360	AGTTTCGCTCTTGTT[G/T]CCCAGGCTGGAGTGC	55298
rs545440379	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927254	CCTGTATCACTCAGG[C/T]TGGGCACAGTGGTTC	55298
rs545467297	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988881	TGCACTCATGAAATT[C/T]TTTCTTCTAGGGGTA	55298
rs545472918	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71958554	CATTGGGATTTTATT[C/G]ATTTATAAGCAAATA	55298
rs545503362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981210	CCTGCCACCACACCC[A/G]GCTAATTTTTTTTGT	55298
rs545567324	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71991696	TAAGAGTCCTGTCAC[A/G]GGAGAAAGTGTGGGT	55298
rs545581359	snp	A/T	1.70542e-05	0.00292007	intron-variant	RNF121	GRCh38.p7	11:71960942	GTCATCAAGAGACCC[A/T]TCCTAAGTATTCTAG	55298
rs545586229	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956746	CAATTTTATTCCTTC[C/T]TGTCCATTTTAGTCC	55298
rs545598663	snp	C/T	0.000214244	0.0103478	intron-variant	RNF121	GRCh38.p7	11:71957294	TCGGGCCCTGCAGTC[C/T]AGGAACTGCAGGTTA	55298
rs545703007	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71986769	GCGAGACTCTCATCT[-/C]AAAAAAAAAAAAAAA	55298
rs545762255	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986202	ACACATCATTTCTTT[C/G]ATTTTTGGCCTGTGG	55298
rs545860960	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950271	TTTTGATGTATGCAT[A/G]TGGTAGTCCCTTGGT	55298
rs545896949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984404	CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACTA	55298
rs546030871	in-del	-/CCTCCCGCTGCCACTGTG	0.00239521	0.0345234	intron-variant	RNF121	GRCh38.p7	11:71994622	CCCGCTGCCACTGTG[-/CCTCCCGCTGCCACTGTG]CCTCTTCTCTAGAAG	55298
rs546069947	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986746	TGCACTCCAGCTTGG[G/T]TGACAGAGCGAGACT	55298
rs546112167	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963564	GTTGGAGGTTGCAAT[C/G]AGCCAAGATCGCACC	55298
rs546134200	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71936107	CCACCTTGGCCTCCC[A/G]GAGTGCTGGGATTAT	55298
rs546176397	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71952117	ACGTGGTATTTATAC[A/G]ATGGAATATTCTTTG	55298
rs546285480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992548	GTTTTGTTATATGTC[A/G]TTTCATTTAAAGTCA	55298
rs546300530	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988378	GGAGCCCTAAGCCTA[C/T]GACAGTGCACTGAAG	55298
rs546338926	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71972664	GTCCACTAGATGATA[C/T]TGGCACCCTTCTGCA	55298
rs546400144	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71965306	CCCAGGTTGGAGTGC[A/G]GTGGTGTGATCTTGG	55298
rs546466407	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929426	GTCTTAGGGTAGGAC[C/T]GAAGGGCTAAGAGGT	55298
rs546499325	snp	A/G/T	0.00676848	0.0578101	intron-variant	RNF121	GRCh38.p7	11:71949863	AAACATTAGCTGGGC[A/G/T]TGGTGGCACGTACCT	55298
rs546538214	snp	A/G	0.00880868	0.065778	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978144	GGGCTCAAGCGATCC[A/G]TCTGCCTCAGCCCCC	55298
rs546613808	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937694	TTTTTAGTCCTTGTC[A/G]TACCTTTTCCCAGAT	55298
rs546669175	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946146	AGAAAAGAAAAATCC[A/G]CACAGAAACTTATAC	55298
rs546732721	snp	G/T	0.00120361	0.0245022	intron-variant	RNF121	GRCh38.p7	11:71967358	TTTTTTGTTTTTTTT[G/T]TTTTTTTTTGAGACG	55298
rs546766877	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71965046	AACAATGTAACAGTA[C/T]GTGACATAGAAATCA	55298
rs546769966	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71931830	TTTACATGTGGCATT[A/G]ATATTGCCCCCTGTG	55298
rs546800219	snp	A/G	7.81953e-05	0.00625232	intron-variant	RNF121	GRCh38.p7	11:71995582	GTCGTTGTTGGGAGT[A/G]GGCTGTGGGAAGAAA	55298
rs546837732	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960692	ATCCCTGGAAAGCAC[C/T]GTCCCTTTATCACTA	55298
rs546853050	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975741	CTTGAAGTGGAAAAG[A/G]TGGGAAAGAAGACAT	55298
rs546887006	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931053	TGGTCAGGCTGGCCT[C/T]GAACTCCTGACCTCA	55298
rs546917913	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974743	TTTCCTTGGATCTCA[A/G]GTACTTTCTCAACCT	55298
rs547096612	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950460	GTGATGGCTTGCACC[C/T]GTAATCCCAGCTACT	55298
rs547102743	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71974233	GGCGTGAGCCACCAC[A/G]CCCAGCCAAGCCCTG	55298
rs547148455	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71961105	CATAAGACTATGTTC[A/G]TAGGCAGAAAAGATA	55298
rs547185792	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935617	ATAGAGTATGACTCA[A/G]TAAATGCTTAAATAT	55298
rs547191393	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71983889	TTCTTCCTATTCTTC[A/T]TATGTTCTACTTTCC	55298
rs547196349	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71936418	TTTTTTAGACAGAGT[C/T]TCGCTCTGTCACCCA	55298
rs547237702	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939364	GCTTACATGGCTTCT[A/G]TAAAGTGACATCTTT	55298
rs547308892	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71990162	GCCCTTTCCTCCTTA[C/T]GGATGGCTCAGCTGT	55298
rs547323589	snp	A/G	3.29511e-05	0.00405887	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990644	TCTCCCTTCTCTTCT[A/G]TGGCCTCTACTATGG	55298
rs547327108	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949873	TGGGCGTGGTGGCAC[A/G]TACCTGTAATCCCAA	55298
rs547407563	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966133	CAAGTGATTCTCCTG[C/G]CTCAGCATCCCGAGT	55298
rs547409216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942891	AAGTTCTAGCAGATA[C/T]GATGTCTGGCAAAGG	55298
rs547528470	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947591	GATGAAAGAGATAGA[C/T]AGTTCAATGTGGCTG	55298
rs547538208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978854	TTAAACGATCTGCCT[A/G]AGTTAACGCAGTAAT	55298
rs547557479	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964546	CAGTATGGCGATTTC[A/G]GCTCACTGCAGCCTC	55298
rs547560905	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71995157	ATCCCTCAGTTTAGC[A/G]TCATCCTCTGTTCTG	55298
rs547564387	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71943397	TTCTGGGACTCTGAA[G/T]ATCTGGCTTTTTATC	55298
rs547580394	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928595	AATACATTTCCGTGT[A/G]TTTTAATATTTATTT	55298
rs547587674	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71986915	ACCCTGGTGTCCCCA[C/T]TGATGTGAGAATAAA	55298
rs547620978	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972953	GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC	55298
rs547667528	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71946565	GAAAGGTCCAGAAAA[A/G]GCAAATATATAGCAG	55298
rs547706822	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994057	GTGTTAGTTAGGATG[C/G]TCTCGATCTCCTGAC	55298
rs547713385	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71992716	CGGCAACTGCTTGGA[C/T]GGTAGTACCTTTCAC	55298
rs547725481	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986449	TGCCTTTTTAGGAAT[C/G]TTTTCCTTGGTCTGA	55298
rs547728389	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973512	AAAAAACAGGCCGGG[C/T]GCGGTGGCTCATGCC	55298
rs547778317	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976394	GGAGTCTCGCTGTGT[C/T]GCCCGGGCTGGAGTG	55298
rs547845099	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976251	TTAGTGTTCTTTGTA[C/T]AGTGTGGCCCCAAGC	55298
rs547910698	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71950713	GCTGGAGTGCAGTGG[C/T]GCGGTCTTGGCTCAC	55298
rs547977600	in-del	-/T	0.0973687	0.197999	intron-variant	RNF121	GRCh38.p7	11:71946648	TAAATGAGCATGAGG[-/T]TTTTTTTTTTTTTTT	55298
rs548193943	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927225	GCACTCCAGCCTGGG[C/T]GACAGAGCCGGACCC	55298
rs548259028	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982650	ACTTTATCCAAAGTT[A/G]TAAATACAGGAGAGG	55298
rs548286721	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953190	AGGCACATGCCACCA[C/T]GCCTGGCTAATTTAT	55298
rs548297267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943475	GCTGTCAGCTTTAAA[A/G]TAATAAAGGCATTTG	55298
rs548324756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955512	AATTCCCTAGGCTAG[A/G]GAATCAGGAAAGTTG	55298
rs548426977	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948877	TGTTATCTTAATCAC[A/G]CAGAATACCACAGTA	55298
rs548438121	in-del	-/T	0.0376206	0.13189	intron-variant	RNF121	GRCh38.p7	11:71980352	CTGTAAAATGACACT[-/T]TTTTTTTTTTAAGAT	55298
rs548563299	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71962312	TGCATATATGCACTG[C/G]AGTAATTTTCAATAA	55298
rs548609528	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933625	TGTTATAGTCCACTG[A/G]TTGGGTGACCCCACT	55298
rs548729936	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987619	ATATTGCCTGTGGCT[C/G]TTTTTCCACTAAAAC	55298
rs548747055	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71993310	GCAACATTTTCACTG[C/T]CTAATTCCAAAATTT	55298
rs548846827	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977043	ATATTGAGCAGAGCC[A/G]TGGAGCATGTCCCAG	55298
rs548874674	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934604	TCTCTAGAGATTTTT[G/T]GTCCAAGCCAATATC	55298
rs548963163	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936538	GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC	55298
rs548979959	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929914	GGGAAGGCTTCCCGG[A/T]GTTGCTGAGTTTTAA	55298
rs549000268	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980837	TCAAAGCCTTAGTAC[C/G]AAAAAAAGTAAGCCA	55298
rs549009194	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937136	TCGGCACTGCTTTCT[G/T]CTCCCGTAGCGCCCT	55298
rs549076187	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987168	GAGTGACTGTTGAGA[G/T]GTACCTCTTGTTGCA	55298
rs549098570	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71951672	CCATGGACAAAGGCT[A/C]TGAATAGACTTTTCT	55298
rs549145821	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930363	AAGATGAGGTTCAGA[A/G]AAAGGGAGAAGTGGA	55298
rs549163038	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71946699	AAATAAGATGGTTGC[A/G]TCTTATTTTATTTAT	55298
rs549164861	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938614	GTAAGTCACTGCTCC[C/T]GGCCTTAATTCTTCT	55298
rs549166708	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974160	GTTAGCCAAGATGGT[C/G]TCAATCTCCTGACCT	55298
rs549266089	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981395	TGCCAGGAAACTAGC[A/C]GCTCTTTCCTCTCTA	55298
rs549302038	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946073	TTATGTTTGTGCCAC[G/T]GCACTCCAGCCTGGG	55298
rs549311358	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960637	GGTACCCTGCAGCTA[A/T]GAAGCAGGGAATGTG	55298
rs549339442	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982117	TCGAAATAGTAGGTC[A/G]GGGCCATACCATGGG	55298
rs549389532	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949078	TTGGACTGTGAATAC[A/G]TCAAGGGCAAAGGTT	55298
rs549438421	snp	C/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71990796	ACTTGTTTAATGGAA[C/G]AGAAAGGCACTAGGG	55298
rs549461524	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963654	GTCTTAGCTCTTACA[C/T]TTGGAGTTTTGGTCC	55298
rs549478292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966783	ATGAGCCACCACAAT[C/T]GGCCTTGCGTTTTTT	55298
rs549478647	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71935642	AAATATGTGAACTCA[C/G]GAAAGATTCCAGTCC	55298
rs549535175	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71956902	TCTATAGCTAGTCTT[C/T]ATTATATAATAGATA	55298
rs549539337	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71967341	TAATAATTATGTGGG[A/T]TTTTTTTGTTTTTTT	55298
rs549543314	in-del	-/CT	0.00159617	0.0282053	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998039	TTTCCCCCCACCCCC[-/CT]GTCAGGCTCAGGTGA	55298
rs549563180	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942032	CCGCCTCCTGGGTTC[A/G]TGCCATTCTCCTGCC	55298
rs549625397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990018	TTTGCCTGGGGAAGG[A/G]GCCAGGTCTCAGGTA	55298
rs549631329	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71960383	TAACCTCTTTGGGTT[A/G]CTTTCTCGTTCCAGC	55298
rs549649977	snp	A/G	4.89992e-05	0.00494946	synonymous-codon, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995484	CGTGGCTGGTGCATC[A/G]TGGGAAAGAAGCAAA	55298
rs549711772	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956412	GGTTTTCAACTAGGG[A/G]GACGCTATGGCAATA	55298
rs549713399	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996063	AGGCTGGGCCCTTCC[A/G]GAAAGCAGCCTCCAT	55298
rs549972687	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71935502	TTGGGTCTTCCTTTC[C/T]GGAGGTGATTTAACT	55298
rs549979379	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71985524	AGAGCTGTGTGTGTT[A/C]TTTAAGACAACACTA	55298
rs549994706	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71988935	GCTCCTGAAGGGTTT[A/G]GAGGAATTCATCACT	55298
rs550007628	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978755	GCTTTCCATGCCTTA[A/G]CTCATTTAACCCATA	55298
rs550058855	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71958262	ATCATGTTATATGAA[C/T]AGTGGTTAAAAGATC	55298
rs550100853	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71965461	ATGTTGTCCAGGCTG[A/G]TCAGGAACTCCTGGG	55298
rs550125276	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974846	TGGTAGGCAGCTTAA[A/G]AGACAGAAAATCTGG	55298
rs550180983	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71938389	GCAGTGGTAGATCTC[C/T]GCTCACCATAACCTC	55298
rs550219870	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927671	GGAGAGGATGAGAGG[A/G]TAATAGGCTTGAGAG	55298
rs550264211	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981983	GCCTGGAAAGGAGAC[G/T]AGACGGAAGGCTTCG	55298
rs550437932	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975453	TGGACCTATTGGCCA[C/T]CAAGACAGAGATCAA	55298
rs550525897	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71931096	ATCTTGTCCTCCCAA[A/C]TGTGCTGGGATTACA	55298
rs550613219	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938560	CCGATCTCAGGTGAT[C/T]CGCCTGCTTCGGCCT	55298
rs550641948	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71989223	ATAGCTGGGACTACA[A/G]GCATGAGCCACCACA	55298
rs550680412	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996750	GGGCTCAAGCCTGGT[A/G]CACTTAGTATAGAAG	55298
rs550689749	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71939418	TTTGCACCGCCCCCC[A/G]CAACTTCCCTCCACC	55298
rs550827081	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71959506	ACCCTGGTGTAATGG[A/G]AATTGTATAAAAGCT	55298
rs550872961	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71931135	TCACCGCGCCCGGCT[A/G]AGAAAATAACATTTT	55298
rs550954728	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940054	TGATTCTTAAAAGTT[C/T]ATCATGTGGATAGGA	55298
rs551100987	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71982116	CTCGAAATAGTAGGT[C/T]GGGGCCATACCATGG	55298
rs551116499	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71957100	ATGGTTGGTAAGGCT[C/T]CATAGAGATACTAAG	55298
rs551119831	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955427	CCAAATGATGCTGAT[A/G]CTGCCAGTCCATGGG	55298
rs551121586	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947066	AGACGGGGTTTCACC[A/G]TGTTGCCCATGTGGT	55298
rs551219468	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932916	TTTTCAGGAGGGATG[A/T]TTAGCCTGTTGGTAG	55298
rs551295954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976459	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	55298
rs551375137	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952021	CAAAAATTTAAAGAT[A/G]GATGTTCATAGTAGC	55298
rs551382491	snp	A/G	6.58935e-05	0.00573955	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987068	GGCATTGTTGGCTAC[A/G]TGGCTGTCATGTTTA	55298
rs551470815	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992828	GAAACGCAAGTAAAT[A/G]TTTCTATTTTTTTTT	55298
rs551528260	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71950532	GAGGTTGCAGTGAAC[C/T]GAGATCATGCCATCG	55298
rs551554982	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71962655	TGCTAACATGATAGC[A/T]CATCTTACACTGAGA	55298
rs551561630	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945994	CTCGTTTCTGTAGTC[A/C]CTGCTACTCGGGAGG	55298
rs551574760	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71980640	GTGTGAGTCACCACG[A/C]CTGGCCATCTAAGGC	55298
rs551575078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973013	CCAACATGGAGAAAC[C/T]TTGTCTCTACTAAAA	55298
rs551606036	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71988175	GGAATTTTGGCTGTT[G/T]CTTCAGTTGTCATAA	55298
rs551633495	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71966261	TGACCTCAGGTGATC[C/T]GCTCACCTTGGCCTC	55298
rs551683957	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952681	AGGCGTGGTGGCGCA[C/T]GCCTGTAATCCTAGC	55298
rs551747802	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972694	ACTTGTAACAACCAG[A/G]TGTCTCCAGACTGCC	55298
rs551771979	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955612	ATAGGGAAGGGCATT[A/G]TAAGTACAAGGAAGG	55298
rs551784359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989748	TTCTTGTTAAATAGA[C/T]TTGGACCAAAATTTA	55298
rs551787073	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985646	ACTTTCCTCCCTAGG[A/G]TTCAGCAGGGTTGGT	55298
rs551803731	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994892	CACATCTCTCCTGCA[A/G]TCTGCACACTGTAGT	55298
rs551833593	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928226	CGCAAGGCTCTTCAG[C/T]TCTCAGTTTCGGGAG	55298
rs551846611	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71969729	CACCCTTGCCTGGCT[A/G]ATTTAAAAATTTTTT	55298
rs551919536	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71959723	TGACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGT	55298
rs551968290	in-del	-/AAATA	0.131381	0.220067	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926908	CTGTCTCAAAAAATG[-/AAATA]AAATAAAATAAAATA	55298
rs551975248	in-del	-/AAGA	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71982482	GAATGCAGGGAGACT[-/AAGA]AAGAGCTCATTGCAG	55298
rs552081831	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956304	GCATTGAGTGACTTA[C/T]GTACTGAGACTTGGG	55298
rs552121968	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998037	TTTTTCCCCCCACCC[C/G]CCTGTCAGGCTCAGG	55298
rs552251322	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984801	AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGA	55298
rs552263856	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985492	CTCTTTTGTGATCAG[G/T]GCAATCCCTGGAGAA	55298
rs552278110	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71980488	AGTAGCTGGGATTAT[G/T]GGTGCCCGCCACCAT	55298
rs552297451	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968892	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTGAGT	55298
rs552338105	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933160	TGAGAGGAATTAGAT[A/G]CACCCTTTTGGCACA	55298
rs552354753	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940971	GAGACGTTAAACAGC[A/G]TGGAATATTCTGGGA	55298
rs552359075	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941688	ACCAAGTCCTGAATG[C/G]TGAAGACCTAGCAAT	55298
rs552385978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991979	AAAAACCTAGCCGGG[C/T]GTGGTGGCACATGCC	55298
rs552455944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964620	GTAGCTGGGACTACA[C/T]GCGCACACCACAGCA	55298
rs552461131	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71980114	ATTTGTTAGTACATC[C/T]TGGTGCTTCCACACT	55298
rs552585611	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934686	CTACCTCTGGATTTT[C/T]TTTAGGCATGTAAAA	55298
rs552642020	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927534	TCAAAGAAAAAAAAA[A/G]AGCACTCAGATTAAA	55298
rs552760328	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71944463	AGGCAAGTAGGGCTT[C/T]CAAATTTATCTAATT	55298
rs552760357	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71973907	CAGAAAATTTTGAAA[A/C]ATACAAAAAACAAAA	55298
rs552792709	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71980329	CTCTTCTCACTGTTT[C/T]TTTTTTCCTGTAAAA	55298
rs552804785	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71973105	GCAGGAGAATCGCTT[G/T]AATCCAAGAGGCGGA	55298
rs552820523	snp	A/G	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71971021	CTAGATTTGTACATA[A/G]TACTGAATACAAAGG	55298
rs552846302	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71947108	GACCTCAGATGACCC[A/G]CCTGCCTGGCCTCCC	55298
rs552856389	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928279	ACAGCTCATCGGGAA[C/G]AGGCTGCTCAGTTCA	55298
rs552871818	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926809	AGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC	55298
rs552903912	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973726	CGGGCAGTGGAGGTT[A/G]CAGTGAGTCAAGATC	55298
rs553096961	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938880	GGATATGTTTGATGA[C/G]CAGATAATCTATTAA	55298
rs553131139	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951469	TGTAGTCCTAGCTAC[G/T]TGGGAGGCTGAGGTA	55298
rs553162877	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71960104	AAGTTTCCAGCTGTA[C/T]TCTCTAGTTACTAAA	55298
rs553164788	in-del	-/CTT			intron-variant	RNF121	GRCh38.p7	11:71975261	TATGAGAAGGAAAAA[-/CTT]CTATCTTCAGAATAT	55298
rs553217480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931249	TACAGAGTATCATGC[A/G]TAGGAGTTAACTTTA	55298
rs553309475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941035	TAAACGTAAGGGGAT[A/G]GCAGTGAGTGACTGT	55298
rs553388014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974479	ACAGCTCTGTAAGGT[A/G]GTCAGGGTAGGTATT	55298
rs553390649	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995073	AGGAACCTGAGGCTG[C/T]AGCTAGTGAGGCTGT	55298
rs553432523	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71934201	TTCCCTCATTTCTCA[A/G]CTTAGTCCTCAAACT	55298
rs553460167	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945535	GTGTGAAGTGTGAAG[G/T]GGATGCTGAACAAGT	55298
rs553504810	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967719	AGCCACTGTGCCTGG[C/T]GGTAATAATTATCTT	55298
rs553510594	in-del	-/TTC			intron-variant	RNF121	GRCh38.p7	11:71983883	TTGCTCTTCTTCCTA[-/TTC]TTCTTATGTTCTACT	55298
rs553524510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988804	TCCAGCTCAGGTGAC[A/G]AAGGGAGACCCCCAT	55298
rs553641412	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975172	AGATTTTTCTTAGAC[C/G]AAGATATTAGGATTA	55298
rs553656803	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71971415	GAACTTTTTTAAAAA[G/T]AAAAATATAAGCAAG	55298
rs553736428	snp	G/T	0.000806777	0.0200683	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978096	TTAAGAGGTGGGGTT[G/T]CACCGTGTTGCCCAG	55298
rs553789323	snp	C/G/T	0.000192141	0.00979968	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978159	ATCTGCCTCAGCCCC[C/G/T]CAATGTGCTCGAATT	55298
rs553840290	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992234	AGGAGTTGCTCCTTA[A/C]AATTTTTACTTTGTG	55298
rs553860354	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991096	GTGGGGACAACGGTT[A/G]AAAAACTATCTGTTA	55298
rs553897365	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950716	GGAGTGCAGTGGCGC[A/G]GTCTTGGCTCACTGC	55298
rs553908607	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71993824	TCTGTATTCATGAAG[A/C]TTCTTTGACACTTCC	55298
rs553977949	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987211	TAACAGGAGGGACGT[A/G]ATATCCAGGATAGGA	55298
rs554001941	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71992989	TATTTCCATCACCTT[A/G]GGTAACTTTAATCTA	55298
rs554057097	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71938908	AATACATCTAAACTC[-/T]TTTTTTTTTTCTTTG	55298
rs554060808	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71963449	AACATGGTGAAACCC[C/G]GTCTCTAATAAAAAT	55298
rs554070026	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927226	CACTCCAGCCTGGGC[A/G]ACAGAGCCGGACCCT	55298
rs554112486	snp	A/G	3.30278e-05	0.0040636	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960782	TGCATGCCAAGCACC[A/G]TGGCCATGAAGCTAT	55298
rs554237025	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967040	CCGCGCCCGGCTAAT[G/T]TTTTGTATTTTTAGT	55298
rs554359418	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975046	AAGCTTTCATCATCT[C/G]TGTCTACTACCAAAT	55298
rs554373684	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71960398	ACTTTCTCGTTCCAG[C/T]ATCAGGTTGAAATAG	55298
rs554380180	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990358	AGAGTGAGGAAAAGG[G/T]GTAGGAGGGGATACT	55298
rs554399450	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936062	CCGTGTTAGCCAGGA[C/T]GGTCTCCATCTCCTG	55298
rs554403283	in-del	-/AT			intron-variant	RNF121	GRCh38.p7	11:71978061	TAGAAACTGAAAAAA[-/AT]TTTTTGTATTTTTTT	55298
rs554404977	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71995762	TTCTCAGCCTCCTTG[C/T]AGCCATTGTCACGGA	55298
rs554424704	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947256	CTCACACCTGTAATC[C/G]GAGCACTTTGGGAGG	55298
rs554488197	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71931470	TGGCAGACCTTAGTT[G/T]GTATTCAGGTTTCTA	55298
rs554546290	snp	G/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71948358	CCATCTTTACTAAAC[G/T]TACAAAAATTAGCCG	55298
rs554612785	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954918	TTGCTTCCCTTAATA[A/G]AGAGAATTTTCTTCA	55298
rs554630079	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71978071	AAAAAATTTTTTGTA[-/T]TTTTTTTTTTTAAGA	55298
rs554635307	in-del	-/A	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71950062	AACCCAAAAACAAAC[-/A]AAAAAATATAAAAAA	55298
rs554764093	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939054	GGATTACAGGCACCC[A/G]CCATCATGCCCGGCT	55298
rs554823968	snp	A/C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978101	AGGTGGGGTTTCACC[A/C/G]TGTTGCCCAGGCTGG	55298
rs554830481	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954076	CTCATGAATCAGTAA[A/G]TATCCTTATCTTGAG	55298
rs554859806	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939213	CTGGCTCATCTAAAC[C/G/T]GTTAAGTTCAGCATT	55298
rs554924240	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71933460	TGTTAAAAGAGAAGA[C/G]TGGACTAGATTGGTG	55298
rs554964529	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71940047	TTTAGGCTGATTCTT[A/T]AAAGTTTATCATGTG	55298
rs554997655	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932971	GCCAGCTCAGCTCAG[A/G]TATTAAACTGGCCAT	55298
rs555132669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932256	CTTTACCTGCATCAT[C/T]TCATTTATTATTAAC	55298
rs555162542	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948471	AGTGACCTGAGATTG[C/T]GCCACTGCACTCCAG	55298
rs555178660	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966162	GTAGCTGGGATTACA[A/G]GCGTGCGCCACCATG	55298
rs555186534	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979106	TCCTTTTCCCATTAA[A/T]TGCAAAATTAATACT	55298
rs555189220	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997050	CCAAGAATAGAGGTC[A/G]TATAGTTGGGCCATG	55298
rs555208995	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936031	TTTTTGTATTTTTAG[C/T]AGAGACAGGGTTTCA	55298
rs555239532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958717	TCCAAAAAAATAATA[C/T]ATGTATATGTACCTA	55298
rs555283686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969177	CAGACGTGAGCCACC[A/G]TGCCTGGCCCCTCTT	55298
rs555350457	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929296	CTCCTGACTTGGGGA[C/G]TCCGAGGCGGCCTTG	55298
rs555371012	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980177	TCATTCAGAGAGTCA[A/G]TTGTGGGTTCCTATG	55298
rs555381805	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71990106	TGTGGCCACCGGAGT[-/AA]TTTTCAGTCTCTGCA	55298
rs555411939	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71964187	CTTTAATCTCTTTCA[C/T]CAATGTTTTGTAGTT	55298
rs555487586	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71943841	GTGCAAGGTGGGAGG[A/T]GAGAAAGAGAATGCC	55298
rs555606564	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71983536	GTATAATTCTTTTTA[G/T]TTTATTCAAATTCGT	55298
rs555643340	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71986538	TTTGGGAGGCTGAGG[C/T]GAGTGGATCATGTGG	55298
rs555649438	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973985	CTTGCTCTTTCACCC[A/C]GGCCAGACTGCAGTG	55298
rs555672095	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71938211	TCATTTAGTGCCCTG[C/T]GAACAGTCTTTTCTC	55298
rs555691355	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973078	GTAATCCCAGCTACT[C/T]GGAAGGCTGAGGCAG	55298
rs555693596	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964904	AGCTCTGAAATCTGT[A/G]TCAAATTGAATTACC	55298
rs555700998	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71948410	GCCCCACCTACTTGG[A/G]AGGCTGAGGCATGAG	55298
rs555782266	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981052	CTAAGAGTAAATACT[C/T]TCTTTTTTTTTTTTG	55298
rs555795923	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930196	TTTGTGATCTTGCAC[A/G]TGCCAGCATATGGGC	55298
rs555889098	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947546	AATTCTAGAGAGAAA[A/C]GACGGCAGCAGCCAA	55298
rs555899089	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71974390	CTGTTATAACACTTA[C/T]AATGAATTGTGGTTG	55298
rs555921626	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930677	ATATATTTGAAGACA[C/G]TTTGGAAAGGGTAAA	55298
rs555938269	snp	G/T	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71934695	GATTTTTTTTAGGCA[G/T]GTAAAATGAGTGGTG	55298
rs555963668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962294	TTCTGAAGAAAGTGA[A/G]TATGCATATATGCAC	55298
rs555975024	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71977210	AGGTATGGTGGGAGG[G/T]TGATCCCTAGCTTAC	55298
rs556033425	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71955698	GATAGGCTTGGTAAG[A/T]TGCAGGTCCAAGTTG	55298
rs556082637	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933907	GCCTAATGGTATATG[C/G]TTTTTTATTAAATGT	55298
rs556092292	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988704	GTGTGCACCTGTATC[C/T]CCAGCTACTCAGGAG	55298
rs556092842	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926923	GAAATAAAATAAAAT[A/G]AAATAAAATAAAATA	55298
rs556135607	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991592	GGCTCAAAGATGGCT[A/T]CCTTGAAGAAGTGAC	55298
rs556163340	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990963	CATAAGCCAGTTAAT[G/T]CAGGAACAGAAAACC	55298
rs556192958	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71993118	TATTGACAGTTTATT[A/C]GGTTCCTTTTTGAAC	55298
rs556224834	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71939386	GACATCTTTCAGATA[C/T]TTTGTGGCTTTTTGG	55298
rs556230171	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71970393	TTGGTTGACACAGTG[C/G]CTTACACCTCTAATC	55298
rs556244175	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971260	GTGATGGTGCATGCC[A/T]GTAGTCCCAGCTACT	55298
rs556250124	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964093	TTTGATTCTCTAGAT[C/T]GTTTGGGGAAATGTT	55298
rs556334234	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71987188	CTCTTGTTGCAAGTC[A/G]TGGTTATTAACAGGA	55298
rs556369017	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71960471	TCATGCTACAGGAAA[G/T]GTGTCAGCTGTTTCT	55298
rs556379622	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992947	CTGTCTCAGTGTCAT[C/T]CCCCAAGACCCCACC	55298
rs556457986	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933141	GGGGAGGCTAACCAA[A/C]CTCTGAGAGGAATTA	55298
rs556458297	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963154	TTCCTCACATTTTAT[C/T]GGTTGTCTTGACACT	55298
rs556462403	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992338	GGGGAAGCTTTCATA[C/T]TTGCTTTGTTAATCT	55298
rs556623491	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71963329	GTTTTCTTTGAAGAG[C/T]TTCATAGTCTTGGCC	55298
rs556625271	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973815	AACAAACCAAAAAAA[A/C]CCCAAAAAACAAAAG	55298
rs556741920	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935035	CAACCTCAGCCTCCC[A/G]GGCTCAGGTGATTCT	55298
rs556752881	snp	C/T	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71942537	GGAGGCTGAGGCGGG[C/T]GGATTACTTGAGACT	55298
rs556756629	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71986010	AGCTGGGATCCACCA[A/G]TTAGGTTGTACACTG	55298
rs556776420	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995708	TAGTCCTGCCCCCAT[G/T]ATACAACCCCAGTTT	55298
rs556778298	snp	C/T			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996791	CTCAGGCTTGTGCCA[C/T]GGGTGAGCACTGAGG	55298
rs556840255	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71947877	TAGAGAAAGAGCAAG[C/G]GATAAAGTCTGAACT	55298
rs556879126	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71966920	CCCAGGCCGGACTGC[A/G]GACTGCAGAGGCGCA	55298
rs556910744	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929575	CCACTAGTAGTATAG[C/G]TTTGAGTTATCTTAA	55298
rs556914894	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988984	TGTCAAAGAAAACAG[A/G]TATCTCCTGGTAACT	55298
rs556977726	in-del	-/AGCAGCTGT	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71948604	GGGTAAAGGGCAGGC[-/AGCAGCTGT]AGCAGCTGTTAGAGC	55298
rs557081712	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932092	TTTCATTAATACTTT[C/T]TCTAGAAGTTGAGAC	55298
rs557091762	in-del	-/TCCTGCCTCAG	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71937420	GGGTTCAAGTGATTC[-/TCCTGCCTCAG]TCCTGCCTCAGCTTC	55298
rs557102243	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983049	GCATGGGGCCTCTCT[A/C]AAACAAGCTGATTGG	55298
rs557106589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952050	GCATTATTTATAATA[A/G]CCAAAAAGTAGAAAC	55298
rs557155187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953817	ATGATATTTTGGGGG[A/G]ACAGGAGACCTGTTT	55298
rs557216445	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946310	CTCCTGATAAGTGCT[A/G]TAACATGGGTGATGG	55298
rs557341065	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952941	ATTTTGAAATGTACA[A/G]TATTCTGTTATGAAC	55298
rs557376360	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989673	ACTCAAGGTTGCAAA[A/T]TATCGGTCCTTGGAA	55298
rs557435910	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71954760	ACAGGTAGTTGCTTT[A/G]TTTTGTTACATAGTT	55298
rs557457904	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934890	TGAGGGTGAAATAAT[A/G]CAGATTACTTATTCT	55298
rs557460844	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980539	TTTAGTAGAGACGGG[A/G]TTTCACCATGTTGGC	55298
rs557464570	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938996	TGCAACCTTTGCCTC[A/C]CGAGTTCAAGCGATT	55298
rs557495359	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961402	CCTATATCTACAAAA[A/T]ATAGAGAAATTAGCC	55298
rs557592620	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942348	AGGTGACTCAGTGAG[A/G]GGGTTAGGAAGTTAT	55298
rs557599945	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF121, LOC100133315	GRCh38.p7	11:71928705	TCCTAGTCCCCACGT[C/G]TCGCTCCTTGGAGCC	55298
rs557619138	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71949275	ATTTAAGAATTAGCT[G/T]GGTGTGGTGGCACGT	55298
rs557656458	in-del	-/A	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71985101	TATTTTTTAATTTTT[-/A]TTTTTAGTAGAGACA	55298
rs557677022	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975874	GGCAGATTTTTCAGG[G/T]CAGCATCAGGAAAGA	55298
rs557679226	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967804	TTAAATAAATATTCA[C/T]TGTTTACATTATTAA	55298
rs557689487	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968317	AAACTGCCTCGGCCT[C/T]GCAAAGTGCTGGGAT	55298
rs557864904	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71982549	GAAAGGAAAGAATAT[A/G]TCCAAGAGATAGTTG	55298
rs557879998	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950787	CCTCCCCAGTAGCTG[A/G]GACTACAGGCAGCAT	55298
rs557880177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958539	TTTCTGTCCCTAAAA[C/T]ATTGGGATTTTATTC	55298
rs557881071	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943794	CAGCTAAAGAAAGAA[C/T]AGAAGAGCCCTCTAG	55298
rs557895083	snp	A/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71993993	CTACAGGCGCCCCCC[A/T]CCATGCCTGGCTAAT	55298
rs557956076	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981009	ACTTGCATGATATTT[C/T]GTTTGGATAGCACTG	55298
rs558020718	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971598	AATCAACAAAAGACA[G/T]CAACTCCAATAGAAA	55298
rs558074330	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978907	TAGATAGCTTTAATT[A/C]TAAAATTTCTGATCA	55298
rs558172270	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71955663	AGAAATGAGTCCCAC[A/G]TGTCTTGGGACAATT	55298
rs558209024	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927507	GCCTTGGTAACACAG[C/T]GAGACACCGTTTCAA	55298
rs558215963	snp	C/T	9.95768e-05	0.00705539	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960880	AAGCAGAGGCACCCA[C/T]GCTCCTACAATGTAA	55298
rs558277366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961340	TTGAGGTGGGCAGAT[A/G]GCTTCAGCTCAGGAG	55298
rs558296940	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929890	TGTGCAACATTTCAG[C/T]TTGGGATAGGGAAGG	55298
rs558321110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937280	TCTTGCACAGTGGCT[A/G]GCATGGAGTAGTTAT	55298
rs558324769	snp	A/G			upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928503	GTAGCACAGGAATGC[A/G]TTCTGGGGCTTCAAG	55298
rs558357015	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71948702	CAGTGTCTGCATGAT[C/T]TCCAGCTGATTTATG	55298
rs558365009	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984257	ATATGTCTGTAATAC[A/G]GAGGATTTTTATAAT	55298
rs558386357	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930039	CATTTAAAGACTGGT[A/G]TATTAAAATACCAGT	55298
rs558386846	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71994119	TGCTGGGGTTACAGG[C/T]GTCAGCCACCGCGCC	55298
rs558442848	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983446	TGAATTTTTGTTGAA[G/T]GAATGAATCTCAGCA	55298
rs558549197	in-del	-/T	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71969396	TGAAGCTTAGCAGTA[-/T]AATATTGAGTGCAAA	55298
rs558599317	snp	A/C	0.162253	0.234095	intron-variant	RNF121	GRCh38.p7	11:71990886	AGTTTGGAAAGCAAC[A/C]CAGCCATAAAAAAAG	55298
rs558607420	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948288	TGAGAGGCCGAGGCA[C/G]TTGGATAACTTGAGG	55298
rs558628644	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971879	CATTGCTGAGTCAGC[A/G]AATATACACATACCC	55298
rs558635107	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977179	TTCATTTCATCCACT[A/G]TATTGCTTTTCAGCC	55298
rs558687939	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977528	TCATCTCAACTGTTT[C/T]AGCCTTGTGGAGGGA	55298
rs558743807	in-del	-/ACAT	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71989595	AATTTATAACTAAGC[-/ACAT]ACATACGGTTCTTTG	55298
rs558773234	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932336	GAGGCTAGAGAGGCT[A/G]AAGAACTTTCCTAGG	55298
rs558792004	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71933060	TGCTAGTAGGATAAG[A/T]TGTGGGTACCAGTTA	55298
rs558968558	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926845	GGCAAAGGTTGCAGT[A/G]AGCCAAGATCACCCC	55298
rs558986467	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979339	TTACTGGGCTTCTAC[A/T]CCACCATCTGGTTTC	55298
rs559022501	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969451	TAAGTTGACACTTTT[A/T]ATAGAAAGGTAAAAA	55298
rs559088199	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997827	TCAGACTGAGGTTGC[G/T]CTATGTTCTCACTGC	55298
rs559141973	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976235	TGGCCATGCTTATTT[A/G]TTAGTGTTCTTTGTA	55298
rs559144716	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949250	TGTGGAGACCCCTTA[C/T]CTACAAAAAATTTAA	55298
rs559144978	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957098	GAATGGTTGGTAAGG[C/G]TTCATAGAGATACTA	55298
rs559148794	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991698	AGAGTCCTGTCACGG[A/G]AGAAAGTGTGGGTGT	55298
rs559152542	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71944997	GTCACTTTTTTGTTG[-/T]TTTTTTTTTTTGAGA	55298
rs559305698	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944006	GTTTGGATTTTTATC[C/T]GTAGCTGATGATTAG	55298
rs559315876	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930101	ATGTTGAGTGTGAAA[A/G]GAATGAAGGGACAGG	55298
rs559399593	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972634	ATAGGATGTTTAATA[A/G]CATCCCTACCCTCTG	55298
rs559427198	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71943428	CTAGCTCTGCCATGC[A/G]GCTGTTATCTGTGAC	55298
rs559445470	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929684	TGAAGGAACAAGTGG[A/G]TGAATAAATGATTGT	55298
rs559451242	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937538	TGTTGAACATCCCCA[A/G]AAAATGGACACCAGT	55298
rs559479336	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71993781	CAAACTCTTTGCTTT[C/T]TTAATTATGATAATG	55298
rs559483992	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71952638	ACATGGTGAAACCCT[A/G]TCTTTACTAAAAATA	55298
rs559489370	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964567	CTGCAGCCTCTACTT[C/T]TGCAGGCTCAGGTGA	55298
rs559494342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960445	GATGCAGGTTTCTCC[C/T]GGGACCTCCTTCATG	55298
rs559605987	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71973552	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	55298
rs559627650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987443	AGAGCTGTTTTTCTC[A/G]TCAGTGTGTACTGTT	55298
rs559632265	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71959882	CTCACGTGATCCTCC[A/G]GCCTCAGCCTCTCAA	55298
rs559683919	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972906	AACATAGGCTGGGCG[A/G]CTGGGTGCGGTGGCT	55298
rs559732852	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71974092	GACTACAGGTGCCTG[C/T]CATCGTGTCTGGCTA	55298
rs559736874	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71963664	TTACATTTGGAGTTT[G/T]GGTCCATTTTGAGTT	55298
rs559753979	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71936048	GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGACG	55298
rs559845197	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940654	GAGTTCTGATATATG[C/G]TAGATACTGTGCTGG	55298
rs559845311	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932733	GTGTTTGTTTCCCTT[C/T]ATTTTAAAGACCCAA	55298
rs559886475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963512	GTAATCCCAGCTACT[C/T]GGAAGGCTGAGGCAG	55298
rs559907931	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71981127	GATCTCGGCTCCCTG[C/G]AAGCTCCACCTCTTG	55298
rs559929647	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976676	TCTGGGTATATTCTT[A/C]GTTAAGCAGGGTTGT	55298
rs559968505	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71975013	GTATCCATCCTATTT[A/T]TGAAGTTCTCCAGGG	55298
rs560025936	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962879	CTTCTTTCACTCCGT[A/T]TTTTTTTAAATTTTA	55298
rs560047581	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937965	GTTCCCTCTAAAGTG[C/T]AGCTTTCCCAAGAGG	55298
rs560154321	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71983674	CCTGTGCTGAGTGCT[A/G]GGGATACAGAGCTGG	55298
rs560162004	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985435	CTTAATCCATATTGA[G/T]TTTTTTGACCTAAAA	55298
rs560218387	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976253	AGTGTTCTTTGTATA[C/G]TGTGGCCCCAAGCCC	55298
rs560243632	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941593	TGAGAAAAGTAATGT[A/C]ATGTGATAAAGATGA	55298
rs560250621	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71984680	GCCTCCCAGGCTTAG[A/G]CGATTCTCCTGGCTT	55298
rs560259350	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956112	TCTACCTGTGTTACT[A/G]TTTCAAATGTTCAAC	55298
rs560300157	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997439	AGCCCTAGTCCTAGG[C/T]GACTTGAATAAAGTG	55298
rs560303566	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71933433	TACCTCTCTTTGGCC[C/G]TGTTTTGCTCTTGTT	55298
rs560354483	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997931	GGCTTCCCATGGTAC[C/T]CTGCTGCTTATGCCA	55298
rs560369309	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71966507	TTTTTTAAGATACAG[G/T]ATCTCAGTCTGTCAC	55298
rs560375629	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986114	ACACACTTTCATCCA[A/C]CTCAAAGGTACTTCT	55298
rs560404106	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970567	CTTGGGAGGCTGAGG[C/T]GGGAAGATTGCTTGG	55298
rs560450942	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950229	CTTGAAGCCAGGGTG[A/G]GAGGCCATCCTCTGA	55298
rs560468679	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71939818	TTATGCCAGGTACTC[G/T]TTTTAGTCTTGGGAA	55298
rs560503138	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931545	CAGCAGGTGAAATCC[A/G]TCTTTAATATGTAAT	55298
rs560560576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971996	ATATCTATCTCTGAG[A/G]GAGTAAATAGGTAAA	55298
rs560586062	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988209	TTCCAAAAGATCTTT[A/T]TTAGCTTACAGGTCC	55298
rs560599405	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995328	ACAGGTTCAGACACA[G/T]GGACTTGCCCAACAT	55298
rs560657819	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928117	GTAAGGCAGAAGCTG[A/G]GGCCGCAGGATGTGG	55298
rs560666380	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71986068	TCCTCCTTCAGGAGC[A/G]TGAACAACCCCATTC	55298
rs560730564	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968162	TGCCCCCGGTTCAAG[C/T]GATTCTCCTGCCTCA	55298
rs560799328	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977977	TCTGCATAACTTTTA[A/G]CCATTTATATGCCTT	55298
rs560811444	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989124	GAGTCTTGCTTTGTC[A/G]CCTAGGCTAGAGTGC	55298
rs560822105	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945076	CACTGCAGTCTGAAC[C/T]TCCTGGGCTCAAGTG	55298
rs560929314	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991171	AGACCTCAGTATCAC[A/G]CAGTATGCCCATGTA	55298
rs560986593	snp	G/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71981433	CTTTTTGTTGTTGTT[G/T]TTTTTAAAAATATTC	55298
rs561052484	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71966630	AGGACTACAGGTACA[C/T]ACCACCACGCTTGGC	55298
rs561081510	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952450	GTATACTTAATTTTT[A/T]AAAATTTTAAATTGA	55298
rs561097259	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930998	CCACCACGCCCGGCT[C/G]ATTTTTTGTATTTTT	55298
rs561102319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939327	GCACACTTACTGACT[C/T]CACAGTTGGAACAAT	55298
rs561161961	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71939899	GTTGGGAGAGGAACC[C/T]ATCAAGTGATAATGA	55298
rs561168515	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974572	CATGACCATTAAATT[A/G]GAGAGTTGGACCTAA	55298
rs561213629	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938423	CTCCTGGGTTCAAGC[A/G]ATTCTTCTGCCTCAG	55298
rs561220314	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975355	GGCTCATTTCTCACA[C/G]CTTCCTCAAATACTA	55298
rs561236532	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961052	TTGGCGAGTGTGTGT[A/C]TAAGGGTCAGGTGAT	55298
rs561379674	in-del	-/CA	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71995718	CCCATGATACAACCC[-/CA]GTTTCCCTATTCTAG	55298
rs561468153	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955178	TACCTGAGAGTGAGT[A/G]CTTCCTTAAATTTTG	55298
rs561536551	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996073	CTTCCAGAAAGCAGC[C/T]TCCATTCCTCTAGGC	55298
rs561697283	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964397	TAATAGTTTTTAAAG[G/T]TTTTTTTAGGATTTT	55298
rs561706189	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931076	TGACCTCAGGTGAGC[C/T]GCCGATCTTGTCCTC	55298
rs561772636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963707	GTGAGATAAGAATCT[A/G]AGTTCATTCTTTTGC	55298
rs561778047	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972786	TAGAGCAACATGGAT[A/G]TTGCAAGCTATGAGA	55298
rs561784474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971878	GCATTGCTGAGTCAG[C/T]GAATATACACATACC	55298
rs561829904	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957414	GATCTCTCTAAGTAT[C/G]TGGGTTGCTCTCTTA	55298
rs561842473	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950436	TAAAAATACAAAAAT[C/T]AGCCAGGCGTGATGG	55298
rs561890787	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71950890	AGAACTTTGGAGTTA[A/G]ACAGATTTTATTTGA	55298
rs561891645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936269	TATAACCTCTTATTC[C/T]ATCACCTTTGACTTT	55298
rs561914299	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993169	TCATTTCCCTCTTAC[C/G]TATTTGTGTAGACAT	55298
rs561942146	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71979514	TATCTCTAGATGTAG[A/T]TTTTTCATCCTAAAA	55298
rs561987494	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994229	AATCCTATCTGAAAG[A/G]CTTGAACCCCTTTTG	55298
rs562001992	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986798	AAAAAAAGAAAAAAA[A/T]TACAAAGCCCTAGTT	55298
rs562041200	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71973308	GACCAGCCTGGGCAA[C/T]GTAGTAAGACCCAAT	55298
rs562051315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966076	CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCAGC	55298
rs562058640	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71959181	GTCAGATTCTCCCAC[C/T]CAGGGTAAAGTTTTA	55298
rs562061935	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979537	TCCTAAAATTTCAAG[C/G]CCAAAAACTACAAAA	55298
rs562112090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959055	CAGAAAAAATATGGA[C/T]TCCTTTTGACAGATG	55298
rs562145550	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71980475	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTATGGG	55298
rs562186686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975478	GATCAAAGGATGCTT[C/T]CTTCAGGCAGCCTTC	55298
rs562196432	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71992662	ACTGAAGGGAAAAAT[A/G]CAAAGGAAATATAGG	55298
rs562234659	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987341	AATCATATTTTCCAA[G/T]GCTTTATATTTTAGT	55298
rs562292936	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71952989	GCAATAGAACTCAAA[G/T]AAAAAACATATTCCT	55298
rs562369040	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932597	TTGTGAGGAAGGTTT[C/T]ATTAGTATTCCCTAT	55298
rs562386065	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71983523	GCAGCCACTGCCTGT[A/G]TAATTCTTTTTATTT	55298
rs562426667	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939090	TTGTATTTTTGTAGA[A/G]ATGGAGTTTCACCAT	55298
rs562483144	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982602	GAGTCAAATATGGTC[C/G]TAAGTCTCTGACTTG	55298
rs562488667	in-del	-/AGTC			intron-variant	RNF121	GRCh38.p7	11:71987313	TCTGAATATATACAA[-/AGTC]AGAGTCCTAAATCAT	55298
rs562528192	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997351	TGTCATTCATGGGTC[C/T]TCCCTGGGCCTGACA	55298
rs562548510	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71988831	CCATCTCGAAAAAAA[C/T]AAAAATAAATAAATC	55298
rs562568211	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989995	AACTCCTACCCTGTC[C/T]CACCCTCTTTGCCTG	55298
rs562590963	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997859	TGAGGACAGTGTCCC[A/G]CCACCACCTGCCTTC	55298
rs562591026	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991296	TCTTTAGGGCCATTA[C/T]AGGAAAGAGCCACTT	55298
rs562644660	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979046	TTTTTCCTGCAGCTA[A/G]CCTGGTAACTCCTAG	55298
rs562657193	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71988116	TTTAGTATTATCCCA[A/G]ATAACGCTGCTCTGT	55298
rs562733060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961835	ATCCCACCTATTGAG[A/G]AGGCTGAGGTGGGAG	55298
rs562733790	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71958315	CACAGGAAAATAGTG[A/G]TAGGAACAGGATGGT	55298
rs562774271	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71964614	TTCCAAGTAGCTGGG[A/T]CTACACGCGCACACC	55298
rs562802342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991730	TTTGAGGAACTAAGA[C/T]CATTGCGGTTGTATG	55298
rs562803598	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71934661	CTGAAGTTTAGTCTT[G/T]GATATCTGACTACCT	55298
rs562841944	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948762	ACTTCAACTTATTAG[C/T]CTTGAATTCTTGGCA	55298
rs562897077	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934559	CCCTATAGACATTTA[A/G]TAAATGTTCCTTGTT	55298
rs563011109	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981458	ATATTCTTTGATTTT[A/G]TTGATGGCATCAGGA	55298
rs563048369	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954341	CCAGATCATGTCTTA[C/T]TCTTAACATTTGTAG	55298
rs563060722	snp	G/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71985183	CCTCCCACTTCAGCC[G/T]CCCAAAGTGTTGGGA	55298
rs563088256	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71981584	GGAGTTAGGAGGCAT[C/T]GGAGAGAAGACTAGC	55298
rs563089943	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928101	GTGTATAAAAAGGAG[A/G]GTAAGGCAGAAGCTG	55298
rs563155289	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984531	ATGATCTGCCTGCCT[C/G]AACCTCCCAAAGTGC	55298
rs563219718	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71941427	TTCCTTCTTCAAATA[C/T]TTGTGACTTCAGTGT	55298
rs563240674	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933591	CTTGAAGCCACCCTT[G/T]GAAAACCAAGGATTT	55298
rs563247237	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71951628	GGCACTATAGCAAGA[A/C]CCTGTCTCTTAAAAA	55298
rs563398616	snp	A/G	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71958911	ATTTTGTGCACATCC[A/G]TTCACTGATATGTTG	55298
rs563401366	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71987500	TGGCCTTACGTTCAA[C/T]TAGGCCAGGGGTTGG	55298
rs563457686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937627	TCTTTGAATGCCTCT[A/G]TTGGAGTGTCCTTCA	55298
rs563484705	snp	A/C	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71937112	AAATTGTTCCTTATC[A/C]GTGAGTCATCGGCAC	55298
rs563517371	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71981339	ACAAGTGTGAGCCAC[C/T]ACGGCCAGCCGAGTA	55298
rs563522380	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930261	TTGTCAGAGATAGAA[A/C]CAGTGAGATCTCTGA	55298
rs563559034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944175	CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA	55298
rs563621584	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945000	CACTTTTTTGTTGTT[G/T]TTTTTTTTGAGACAG	55298
rs563648582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966654	GCTTGGCTAATATAT[A/G]TATATTTTAATTTTT	55298
rs563667554	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71930955	CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAT	55298
rs563729337	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974153	TCACCGTGTTAGCCA[A/G]GATGGTCTCAATCTC	55298
rs563813304	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958656	CCTTGAGCCCAGCAG[C/T]TCGAGGCTGCAGTTC	55298
rs563830354	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960980	CCTAACCCAGGCCAC[A/G]TGGAGGTGGAGAAAG	55298
rs563874182	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996049	CTGAGTAGGAAGTGA[G/T]GCTGGGCCCTTCCAG	55298
rs563880034	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71956678	ACTCTGTCTCCCACT[A/T]ATCCTGATTCATACT	55298
rs563901860	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71984507	AGGATGTCTCGATCT[C/T]CTGACCTCATGATCT	55298
rs563913823	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957347	GTCTACCCATTTTGC[C/T]TTCTTGTCAGTAGGA	55298
rs563913885	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949500	CAGGCAGATCACTTG[A/G]GGTCAGGAGTTCAAG	55298
rs563954259	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970614	CTTCAGTAAACTATG[A/G]TCACGTCACTGCACT	55298
rs563976410	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975437	GATGCCTTTTTCTAT[C/T]TGGACCTATTGGCCA	55298
rs563997359	in-del	-/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71993698	AGTTTCATATCTTTT[-/G]GGTTTATACCGAGAA	55298
rs563999781	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71960551	CTTGGTTGCTGGGGG[C/G]TCCGTAGAGCCTGTA	55298
rs564121303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71976807	TTCCTTCCCCATTCT[A/G]TACTTTGGTAGTTAG	55298
rs564183457	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977683	TGTTTCTCCTTCTAC[C/T]TGGCCAAACCCATTC	55298
rs564213827	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963593	CCACTGCACCCCAGC[A/C]TGATAACAGAGCAAG	55298
rs564222194	snp	A/C	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71969730	ACCCTTGCCTGGCTA[A/C]TTTAAAAATTTTTTT	55298
rs564227859	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71950280	ATGCATATGGTAGTC[C/T]CTTGGTAGATTTTTA	55298
rs564234422	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71934129	CTTCTTGGACTATTC[C/T]GATCTACACTGCTAC	55298
rs564344568	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71945279	CAGGCATGAGCCAAC[A/G]TGTCTGGCCAAGATT	55298
rs564366533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973140	GTGGTGAGCCGAGAC[C/T]GTGCCTTTGCACTCC	55298
rs564407994	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71964282	GCCATTGTTAATGGA[A/T]TTTTTAAAAATTTCC	55298
rs564466669	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943176	GTGGATAAATTTAGA[A/G]TATGTTTTGAAATAG	55298
rs564493083	snp	C/G	0.00438332	0.0466095	upstream-variant-2KB, nc-transcript-variant	RNF121, LOC100133315	GRCh38.p7	11:71928376	TCACCCGGGACCGTG[C/G]ACCTCGAGGAGCCAC	55298
rs564518611	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71989179	CCCGAGTAGTGGGGT[A/C]AAATGATTCTCCTGC	55298
rs564528121	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936118	TCCCAGAGTGCTGGG[A/T]TTATAGGCGTGAGAT	55298
rs564542091	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986756	CTTGGGTGACAGAGC[A/G]AGACTCTCATCTCAA	55298
rs564552576	snp	A/C	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71965329	GATCTTGGCTCACTG[A/C]AACCTCTGCCTCCTG	55298
rs564588005	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978470	AAACATTAATAAGAA[A/G]TTGCTTATAACCTTA	55298
rs564677434	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71976067	TGTCTGTTTATTGGG[C/T]CTCTGGATGACTCTT	55298
rs564705910	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71995948	CCCCTCTATCTGCCT[C/G]CCACCTTCTCTGCAT	55298
rs564727502	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946024	GCTGAGGTGGGAGTA[A/T]CACTTGAGCCCAGGA	55298
rs564733939	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950261	TGATAGATATTTTTG[A/G]TGTATGCATATGGTA	55298
rs564739945	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939164	CCACCTTGGACTCCC[A/C]AAGTGCTGGGATTAC	55298
rs564765655	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975993	CAACCGTGTTTCTGC[C/G]TTGTAGAGTGTCCAG	55298
rs564769132	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71952675	TTAGCCAGGCGTGGT[A/G]GCGCATGCCTGTAAT	55298
rs564790329	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982538	GAGCTCAAATGGAAA[G/T]GAAAGAATATATCCA	55298
rs564797743	snp	A/G	0.00159617	0.0282053	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929018	TTGAGCAGCGGAAGC[A/G]GCTGGCTCGCGCGGG	55298
rs565114278	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968101	AAGTCCTGCTCTGTC[A/G]CCCAGTTTGGAGTGC	55298
rs565120904	in-del	-/A	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71963827	CAATTGATCAAAGAT[-/A]ATGTTGGCTTATTTT	55298
rs565222856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968549	ATTCTCAAATCTGCT[A/G]TAGGTTAAAGGTCAG	55298
rs565235023	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71961718	AGAAGACAGAAATTG[A/G]CAGATTGGTTTTAAA	55298
rs565254336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955302	CTAACATAGAACAGT[A/G]CTTCTCAAATTTAAT	55298
rs565286944	snp	C/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996709	GCTGAAGGCCTCAGC[C/G]CACCCACTCCCTTCT	55298
rs565288191	snp	A/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71940707	CTCCTGCTCTCACGA[A/G]ATTAATAGTCCTGTG	55298
rs565328190	in-del	-/AAAACA	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71979549	AAGCCCAAAAACTAC[-/AAAACA]AAGCAAGATTTTTCA	55298
rs565336727	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71943355	TGGAAATACGAGCTT[A/G]TAGCTCAGGGAGAGG	55298
rs565386238	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931441	CAAGCTCCAAAAATA[A/G]CAGAGGTCTGGTCTG	55298
rs565406832	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997164	CCAGCGGTCACTCTG[A/C]CACATCACTTCCTTC	55298
rs565516233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984420	AAGTAGCTGGGACTA[C/T]AGGCACCCGCCACCA	55298
rs565541180	snp	C/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71990651	TCTCTTCTATGGCCT[C/G]TACTATGGAGTTCTG	55298
rs565549238	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947815	TCATGAATCTGTGCT[A/G]GCAAAGTTAGAGTCG	55298
rs565556094	snp	C/T	9.70167e-05	0.00696412	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929102	TTGGAGGTGGTGCTG[C/T]TGGGGAACGGGAGCT	55298
rs565610685	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940018	TTAAAGAAGACTTCC[A/G]ATAGGGTATGGCATT	55298
rs565615231	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934858	TTCTGAGGCCAGGGC[C/T]TAGCAGAAAAGAGTG	55298
rs565635889	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950498	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	55298
rs565681379	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985821	GTTTGGCCAAGCACC[A/C]GTGGCTTATGCCTGT	55298
rs565714661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978861	ATCTGCCTAAGTTAA[C/T]GCAGTAATTAGCTGT	55298
rs565762286	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958464	AAGAAGATAGATTTT[A/T]TTTTTGTCTCATTGT	55298
rs565769022	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957012	ATTGCCTAGCACAGA[C/T]GTGCAACACATTCAG	55298
rs565777458	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972468	TCCTTCACTAGTGCA[C/G]GTTGGTGGCGCAGCC	55298
rs565787005	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964734	TCCGCCTGCCTCAGC[C/T]TCCCAAAGTGTTGGG	55298
rs565860316	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986939	GAATAAAGGATTCTG[A/G]TGATCAGGACCATTA	55298
rs565880584	snp	A/C			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996526	TTTTAAAAGAAAACT[A/C]TTTTGATGAATATAT	55298
rs565976935	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966161	AGTAGCTGGGATTAC[A/G]GGCGTGCGCCACCAT	55298
rs565991927	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71939012	CGAGTTCAAGCGATT[C/G]TCCCACCTCAGCCTC	55298
rs566033243	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951868	CCCTCACACACTGCT[G/T]GTGGGACTGTAAAAT	55298
rs566117478	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972963	AGGCCGAGGCAGGCG[A/G]ATCACGTGAGGTCAG	55298
rs566147682	snp	C/T	6.59033e-05	0.00573997	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994727	CCTTCAGTTCTACAG[C/T]GAGTCGGGCATGCCT	55298
rs566165677	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961311	CATGTTTGTAATCCT[A/C]GTACTTTGGGAGATT	55298
rs566192257	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71967632	TTCACCATGTTGGCC[A/G]GGATAGTCTCGATCT	55298
rs566242757	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71951166	GAGGCAGAGGTTGCG[A/G]TAAGCCGAGATTGTG	55298
rs566326766	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927394	CAGGCGTGGTGGCGC[A/G]TACGTAGTCCCAGCT	55298
rs566427249	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962085	CCATTCTCCTGCCTC[A/G]GCTTCCCGCATAGCT	55298
rs566469418	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71964499	CTGAGACAAGGTCTT[A/T]TTCTGATTGCCCATA	55298
rs566540209	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996792	TCAGGCTTGTGCCAC[A/G]GGTGAGCACTGAGGC	55298
rs566591634	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984159	GGGTGATAAGATGAT[A/T]TGAAGAAAAAGTGCA	55298
rs566593505	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991348	TCATTCAGTAGATAC[C/T]TTTTAATGCCTGCTA	55298
rs566657368	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955517	CCTAGGCTAGGGAAT[C/G]AGGAAAGTTGCAGTT	55298
rs566748180	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71954944	CTTCAATTCCACAAG[C/T]ACTCATTGAGTGCTT	55298
rs566767554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985943	AGCCAAAAAAAAACA[A/G]AAAAAAAGGCCCTGG	55298
rs566787622	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996379	GGGCACTCTCCTCCC[C/T]GCCCACAAAGACCTC	55298
rs566832974	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940159	ATTCCTCACTAATGA[C/T]ATATTTACTGATAAC	55298
rs567009420	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932988	ATTAAACTGGCCATG[A/T]TGACTGCCTAAGCTC	55298
rs567014671	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71970157	TGATTCCACTTATAT[A/G]AGATATCTAAAGTAG	55298
rs567019691	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931657	AGACATGCAAATAGC[A/G]TATTATAATACTAGA	55298
rs567095051	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956539	AACGAGAACTTTGAA[A/G]TCGGATGGCTAGTGA	55298
rs567103577	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929405	TTTTGTGATTACTAG[C/T]TGGGTGTCTTAGGGT	55298
rs567107014	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963868	GTTTTATTCCGTTGA[A/T]CTATATGTCTGTTCT	55298
rs567178229	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71970826	CCAAGACAGGGACTT[A/T]CCTTGCCTTAAGACA	55298
rs567178522	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927488	ATTGAACCAGTGCAT[C/T]CCAGCCTTGGTAACA	55298
rs567182386	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982562	ATATCCAAGAGATAG[C/G/T]TGAGTGAGGGATGAA	55298
rs567224715	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937164	CCTGTACAGATTTCC[A/G]TCAGCACTTACCATG	55298
rs567302888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980871	CATAAATAATTTTAA[C/T]CTTGAATACATATTG	55298
rs567350927	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943611	AGACATAGGCCTTGC[A/T]CTCAGGTTGCTCATG	55298
rs567475752	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71931195	AGCTTTTCTTTATTG[C/T]TTGAAGGACTTGAGA	55298
rs567504674	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959387	TATATTTGCTTTATT[A/G]TTTATAATTCATCCT	55298
rs567504736	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966848	CTTTATTATATTTAA[A/G]TATAATATTTGTGGG	55298
rs567513876	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71973644	ATACAAAAATTAGCC[A/G]GATGTGGTGGCAGGT	55298
rs567537131	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931742	ACTTGAGTCAGCTAG[G/T]GGGAGTCAGTAAAGT	55298
rs567589589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966321	GCCGTGCCTGGCCTG[A/G]TATTTCCATTTTTAT	55298
rs567618241	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945410	TGGCTTTCCCAGTTC[C/T]TCTGGATTCTTCTGC	55298
rs567622059	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71935779	ATGTTTCTTATAACT[A/C]TCATCAGGTACTGAG	55298
rs567660244	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995041	TAAACAGTGGTTACA[A/G]CCTGGCTGGGTCTGA	55298
rs567663777	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71988703	AGTGTGCACCTGTAT[C/G]CCCAGCTACTCAGGA	55298
rs567717802	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71965171	CCATTAGGTTCTGCG[G/T]CATTTTTCACCTAAT	55298
rs567752306	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952865	AAGCTAGTAACTTAT[C/T]GATCACCTCAAATAC	55298
rs567754230	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71938162	TTTTACTCCCTGTTG[C/G]CCATAGGATTGAGCC	55298
rs567758981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960010	CTGTTCTTAGAACAA[A/G]TTTTTAGCCAGTATT	55298
rs567895940	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71975112	TTTCCCTCCTGGAAC[C/T]GGTGAGTGGCAAAAT	55298
rs567930543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989419	ATTCTTCTATAATTA[C/T]AGTTTCTTTTTACTT	55298
rs567980654	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926826	GAATCACTTGAACCC[A/G]GGAGGCAAAGGTTGC	55298
rs567992947	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941028	TTTAGGTTAAACGTA[A/T]GGGGATAGCAGTGAG	55298
rs568055338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942089	AGGTGCCTGCCACCA[C/T]GCCCAGCTATTTTTT	55298
rs568058033	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997708	GTGGTTGGGCCTGCC[C/T]TTCTGCTGTTCCCAG	55298
rs568058521	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962949	GTGTTGATTTGTATT[G/T]CCCTAATGACTAATG	55298
rs568068653	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991630	CTGACTTGAACAATG[A/G]ATAGCAGTTAAGTGG	55298
rs568128331	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71977549	TGTGGAGGGATAAGC[A/G]GGATATTGCTATTCT	55298
rs568150055	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985548	AACACTAGAAGGAAG[A/T]TATTTGGGACCTTTC	55298
rs568150636	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964698	TGCCTAGGCTGGTCT[C/T]GCCCTCCTGAACTCA	55298
rs568174992	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71971286	CTACTCAGGAGGCTG[A/T]GGTGGAAGGATCACT	55298
rs568193231	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71946319	AGTGCTATAACATGG[G/T]TGATGGGTGATCCTT	55298
rs568199441	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935519	GAGGTGATTTAACTG[A/G]AGTCATGGTATTTGT	55298
rs568209292	snp	C/T	0.0028028	0.0373302	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978138	GCTCCTGGGCTCAAG[C/T]GATCCATCTGCCTCA	55298
rs568225855	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71954469	TACTGTCCTCTGCTT[C/T]ACCAACATTCAATTA	55298
rs568248266	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71991533	GTAGGAAAGGTTCAT[G/T]ATGCTGTAAACACAT	55298
rs568278632	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71944152	GCTTGGGCAACATGA[G/T]GAAACCCCGTCTCTA	55298
rs568295249	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986328	ACAACTAGCCTTCCC[C/T]GCCTGTTAATCTTCT	55298
rs568324565	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993563	TGAATAGTATTCCAT[C/T]GTGTGTGACACCGCA	55298
rs568446971	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927674	GAGGATGAGAGGGTA[A/C]TAGGCTTGAGAGTAG	55298
rs568545175	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71967575	TAGTATTTAGTATTT[C/T]GTATTTAGTACAAAT	55298
rs568571678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974362	TGATGATTTAAAAAA[C/T]ACTCCACCTACTCTG	55298
rs568606928	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951131	CGGGACGCTGAGGTG[G/T]GAGAATCGCTTGAAC	55298
rs568614005	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980423	GCGATCTCAGCTTGC[C/T]GCAACCTCCACCTCC	55298
rs568632489	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974960	TCTTTAGCTCCTTCA[A/G]GGATGTTAGGGGAAG	55298
rs568664034	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950714	CTGGAGTGCAGTGGC[G/T]CGGTCTTGGCTCACT	55298
rs568744350	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958343	GGTTTTGTTTTGTTT[C/G]AATAACATCATGATA	55298
rs568984392	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996762	GGTGCACTTAGTATA[A/G]AAGAGCTAACGTACT	55298
rs568989133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954858	TGTTTGTTTACTCTG[C/T]ACAATTTAAGCATCT	55298
rs569004926	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71936515	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	55298
rs569041335	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980879	ATTTTAATCTTGAAT[A/G]CATATTGAGATATTT	55298
rs569075294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961229	AAAACTAAGCATCTC[A/G]TGAATCTTACAGGAT	55298
rs569168788	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71970276	GTTCTGGAGATCTGT[C/T]ACAAAATAGTAACAG	55298
rs569173913	in-del	-/AAAAA	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71985942	TAGCCAAAAAAAAAC[-/AAAAA]AAAAGGCCCTGGTTC	55298
rs569201242	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71984103	TCTGAGCCTTGAAGT[C/T]TTCATCCCTAAAAAT	55298
rs569218077	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71983078	GGTAGAACCCCTCCC[C/T]TATTTATCGATTAAA	55298
rs569287203	snp	C/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71950715	TGGAGTGCAGTGGCG[C/G]GGTCTTGGCTCACTG	55298
rs569308842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990330	CCAGTTAGGGGAGGC[A/G]AGGACTAAGAGCAGA	55298
rs569368885	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947118	GACCCGCCTGCCTGG[C/T]CTCCCAAAGTGTTAA	55298
rs569378709	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71953208	TGGCTAATTTATTTA[-/T]TTTTTTGTAGAGATG	55298
rs569395811	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LOC100133315, RNF121	GRCh38.p7	11:71926714	GAGACCAGCCTGGCC[A/G]ACATGGTGAAACCCT	55298
rs569412788	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71957445	GTCTTGAATGTGTAA[A/G]CAGATGATTGCACCA	55298
rs569422966	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71984951	AATAGAGATGAGGTC[A/G]CACTCTGTCGCCCAG	55298
rs569466043	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71961967	CTAATCTGCAAAGAT[-/T]TTTTTTTTTTTTTTT	55298
rs569519751	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71936003	CAGGTGTGTGCCACC[A/G]CGCCCGGCTACTTTT	55298
rs569535773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71986543	GAGGCTGAGGCGAGT[A/G]GATCATGTGGTCAGG	55298
rs569635385	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987111	TTAACTTATTATTCA[A/G]GTGAGTACCCTTTGT	55298
rs569642928	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71943500	CATTTGTTACGCCAG[C/T]CTCGTGTATGTTGGG	55298
rs569713230	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929774	GGGCCAGGTGCTAGG[C/G]AGACAAGGGGCCCCT	55298
rs569763860	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950547	CGAGATCATGCCATC[A/G]CACTCCAGTCTGGGC	55298
rs569793051	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71965658	TTAGTAAGCTTCTCA[C/T]ACATAAATTACCTGC	55298
rs569845387	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71973042	AAATACACTGTTAGC[C/T]GGACATGGTGGTGCA	55298
rs569845429	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980713	AGACAACTAAACACT[A/G]AAACTGCTCTAAGCT	55298
rs569907498	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71973578	GATCACCTGAGGTTG[A/G]GAGTTCAAGACCAGC	55298
rs570008141	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944606	GGTCATGGCCTTGTG[C/T]GGTCCCAAGAGCTCA	55298
rs570022620	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945293	CATGTCTGGCCAAGA[C/T]TCACTTTTATTTATT	55298
rs570097798	snp	A/C/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71990451	ATAAAAATAGACAGC[A/C/G]GACTGGATTTGGTCA	55298
rs570148762	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955617	GAAGGGCATTGTAAG[A/T]ACAAGGAAGGGTATG	55298
rs570151719	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71959348	ACACCTTTATACTTA[C/G]CACCTGGGTTCTACA	55298
rs570184211	snp	C/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928318	ATGGCCACCCTCCTC[C/G]CTCTCGGCCACTCCC	55298
rs570201842	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989247	CACCACACCCGGCTA[A/T]TTTTTATATTTTTAG	55298
rs570217476	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988551	GCTCTCACTTGTAAT[C/T]CCAGCTATTTGGAAG	55298
rs570259711	snp	C/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71975659	TCTGAATTCCCCAGT[C/G]ATTAGCATGGCATCC	55298
rs570324070	snp	G/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929293	GCACTCCTGACTTGG[G/T]GACTCCGAGGCGGCC	55298
rs570336327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994934	AGAGGGTGGTCATGA[C/T]CCTAGGCATGCTGTC	55298
rs570349407	in-del	-/G	0.00123558	0.0248247	intron-variant	RNF121	GRCh38.p7	11:71970818	GCAACTACCAAGACA[-/G]GGGACTTACCTTGCC	55298
rs570411625	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948332	ACCAGCCTTGTCAAC[A/G]TGGTGAAACCCCATC	55298
rs570423619	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949004	AGCATTTTGTGTATA[C/T]GTCAAAGGTTATCCT	55298
rs570442062	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996932	TCAGTGACTTGGCCA[A/G]CAAGGGAAGCCTTGG	55298
rs570460156	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953500	ACTTTAATGTACATA[C/T]GAATTATTTCAGTAT	55298
rs570616558	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71980275	GGAACCTCTAAAGCA[A/C]AGTGGTTCTGCTTAC	55298
rs570764950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972127	AAAAACTAAGAAACA[A/G]AAAGATGTGTAACAC	55298
rs570798588	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971131	ACTCATGCCTGTAAT[C/G]CCGGCACTTTGGGAG	55298
rs570843728	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71933826	TAAGTATTTGATAAT[C/T]GTTGTTTTTGATTAA	55298
rs570929608	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71951000	GAGGCTGAGGTGGAC[A/G]GATCACCTGAGGTCG	55298
rs570973775	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980905	TATTTTGTATGTATT[C/G]GAATAAATAAAATAT	55298
rs571002338	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926865	AAGATCACCCCTCTG[A/T]ACTCCAGCCTGGGTG	55298
rs571043212	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71947196	AATATACTAACAATA[A/G]TTGAATTTCTTACTT	55298
rs571059326	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957583	AGGATCATAACAATA[G/T]CTATACCTCATAGAG	55298
rs571139659	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964622	AGCTGGGACTACACG[C/T]GCACACCACAGCACC	55298
rs571283995	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71938696	AAGCTTTTGTTTCAT[C/T]CATTTCTTCTGGGAT	55298
rs571295776	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937898	TTTCCCTTGAAGTCA[C/T]TTGCTACCTCTACTC	55298
rs571297112	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937219	GGGAACTCCTTGAGG[A/G]GACTGCACCTTATCA	55298
rs571370203	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71940226	GGTTGAGAGAAAACC[A/G]TGTTTCTTGCATTCA	55298
rs571406685	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930023	TTACCTATCTAATAG[A/G]CATTTAAAGACTGGT	55298
rs571459669	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932885	TACTGATAACTGGTG[G/T]ATTCTGCTGAACCCC	55298
rs571464473	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71967380	TTTGAGACGGAGTCT[C/T]ACTCTGTCACCCAGG	55298
rs571540038	snp	C/T	0.000116245	0.00762293	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996173	TCTTGCACAGAGTCT[C/T]TTTTCTTTAACACAC	55298
rs571550612	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990178	GGATGGCTCAGCTGT[G/T]TCAACTTGAGTGGCT	55298
rs571588410	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71938891	ATGACCAGATAATCT[A/G]TTAATACATCTAAAC	55298
rs571737987	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995615	ACTGGCCAGTGTGAC[A/C]TGCATTTGGGTCCTC	55298
rs571760805	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71988994	AACAGATATCTCCTG[A/G]TAACTTTCTAACCTG	55298
rs571767800	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953789	GCCTACAGATGCAGA[A/G]ATCATAGGGTTTATG	55298
rs571849514	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71975755	GATGGGAAAGAAGAC[A/G]TAGTTCTAGGTATTA	55298
rs571888040	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963558	CAGGGAGTTGGAGGT[A/T]GCAATGAGCCAAGAT	55298
rs571908076	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71976425	CAGTGGCACAATCTC[A/G]GCTCACGGCAACCTC	55298
rs571948329	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71977512	TTAGCATCTAACATC[A/G]TCATCTCAACTGTTT	55298
rs571988207	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927235	CTGGGCGACAGAGCC[A/G]GACCCTGTATCACTC	55298
rs572059217	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71984947	TAAAAATAGAGATGA[A/G]GTCGCACTCTGTCGC	55298
rs572184295	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971443	AAGTAAGAAAGATTC[A/C/G]ATAAATTTGATTTTA	55298
rs572192148	snp	C/G	0.00142573	0.0266615	intron-variant	RNF121	GRCh38.p7	11:71960742	CACCCCATGTGTTTG[C/G]CTTTCAGGGTCGAGC	55298
rs572202409	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71991691	ATTCATAAGAGTCCT[A/G]TCACGGGAGAAAGTG	55298
rs572202430	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71984355	GATCTCGGCTCACTC[A/G]TGCAAGCTCCGCCTC	55298
rs572211598	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970582	CGGGAAGATTGCTTG[A/G]GCCCAGGAGTTTAAC	55298
rs572238411	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994062	AGTTAGGATGCTCTC[A/G]ATCTCCTGACCTCGT	55298
rs572260952	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71968128	GTGCAGTGGCATGCT[C/G]TCGGCTCACTGCAAC	55298
rs572267430	snp	A/C/G	0.000191516	0.00978372	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978162	TGCCTCAGCCCCCCA[A/C/G]TGTGCTCGAATTACA	55298
rs572298305	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979255	CCAATCCCTTCCTCC[A/T]AGAAAGGACGGAGGA	55298
rs572301470	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992512	ACTCTTGTTTCTATC[A/G]ATTAGCCTGTGGTAA	55298
rs572384107	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71942678	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	55298
rs572460609	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71995346	ACTTGCCCAACATTA[C/T]AGAGCTGATAAAGAG	55298
rs572558873	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972656	TACCCTCTGTCCACT[A/G]GATGATACTGGCACC	55298
rs572628062	snp	C/G	1.64917e-05	0.00287151	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, stop-gained	RNF121	GRCh38.p7	11:71960822	AATGGTCCTCATCCT[C/G]ATCGCAACCTTGGTG	55298
rs572648805	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928953	TCTCCGCCTGTGTTG[A/G]TGCCCCGCCCCCTCT	55298
rs572649275	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936664	CTCCCAAAGTGCTGA[A/G]ATTACAGGCGTGAGC	55298
rs572690757	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71982499	GAAAGAGCTCATTGC[A/G]GTCAGCCAGCCAAGT	55298
rs572703243	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71983385	ATTTTGTTTGTCACT[G/T]TATATTCAGGCCCTG	55298
rs572755545	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987766	GACCGTGGTTGGCTA[C/T]AGCTAGCAACAAATT	55298
rs572769433	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995802	TTGTGTCAGCCTCAG[A/G]CTGTGTTATCTTACA	55298
rs572787215	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71936106	CCCACCTTGGCCTCC[A/C]AGAGTGCTGGGATTA	55298
rs572822644	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945884	TTGGGAGGCTGAGGA[G/T]GGTGGATCACTTGAA	55298
rs572907182	snp	C/G/T	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71953143	GGCTTAAGCAGTCCT[C/G/T]CTGCCTTAGCCTCCC	55298
rs573035919	in-del	-/CCT	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71979271	AGAAAGGACGGAGGA[-/CCT]CCTTAGGGTGACCTA	55298
rs573037509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939496	TTAATATCTTGATTT[A/G]CATGATTTTGTGGGG	55298
rs573041204	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946475	CACAGGATTTTCCCC[C/T]GTCACCCTCCACAGA	55298
rs573091914	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71959067	GGACTCCTTTTGACA[C/G]ATGAAGAAATTGTGA	55298
rs573126756	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71942883	TAAAGGCAAAGTTCT[A/G]GCAGATATGATGTCT	55298
rs573197495	snp	A/G	0.00133042	0.0257573	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978197	TGAGCCACCATGCCC[A/G]GCCTACAGTAGAAAT	55298
rs573211584	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71957548	TTCTCACAACCTTAC[G/T]TTGCCCCATTTGTAA	55298
rs573221613	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975943	TTATGTGGTAAGGAT[C/T]ACTATGTGTAGGTGT	55298
rs573228011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969251	AAATGACAATACTCA[C/T]GTAAAGGTGAATGGG	55298
rs573293824	snp	A/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927643	CTAATTCTAATTCAT[A/T]ATAGTTGCTTCTGGA	55298
rs573314140	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961593	AAAAACAGTAATGGT[G/T]GAAATTAGGTGGGGA	55298
rs573332575	in-del	-/TT			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929945	CGATAAATAAGTGTC[-/TT]TCTCTCTTCTTCTGG	55298
rs573394048	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71948551	AAAAGCTTATCAACT[C/T]AGCTGGCCAGGAGGT	55298
rs573490043	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71939133	GATCTCGAACTCCTG[-/A]TCTCAGGTGATCTGC	55298
rs573528029	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962434	ATATGAAGGTTGGGT[A/G]ACCCTAACACCTCTG	55298
rs573604973	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71955810	GCTCAGGTACCTCCC[A/G]TGTGTCCCCTCAGAG	55298
rs573727977	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71964953	GTCTTGTTCTTAGAG[A/G]ATGAAGCAGACCTGC	55298
rs573759123	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936032	TTTTGTATTTTTAGT[A/G]GAGACAGGGTTTCAC	55298
rs573795953	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936933	AGTAAATGAGAATGC[C/T]TGTAGATGTGGATTC	55298
rs573896925	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71993768	TTTGAGGACATGCCA[A/G]ACTCTTTGCTTTCTT	55298
rs573903318	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71958718	CCAAAAAAATAATAT[A/G]TGTATATGTACCTAC	55298
rs573955877	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71933145	AGGCTAACCAACCTC[C/T]GAGAGGAATTAGATG	55298
rs573980378	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981079	TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG	55298
rs574038839	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930679	ATATTTGAAGACACT[G/T]TGGAAAGGGTAAATA	55298
rs574138447	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71974425	TTTCTCCTCAGTAGA[C/G]TTGAGTTCTTCTCAT	55298
rs574185331	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947596	AAGAGATAGATAGTT[C/T]AATGTGGCTGGAATG	55298
rs574200801	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948422	TGGGAGGCTGAGGCA[A/C/T]GAGAATCGCTTGAAC	55298
rs574215596	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994220	ACCATGCTAAATCCT[A/G]TCTGAAAGGCTTGAA	55298
rs574220474	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71981276	AGGATGGTCTCAATC[A/T]CCTGACCTTGTGATC	55298
rs574277687	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969589	TTATTTTGAGACAGG[G/T]TCTTTCTCTGTCACC	55298
rs574340797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970407	GGCTTACACCTCTAA[C/T]CCCAGCACTTTGGAA	55298
rs574420854	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71937887	CTTCTTTATGTTTTC[C/G]CTTGAAGTCATTTGC	55298
rs574445968	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997896	ACCACACTCAGGCTC[A/G]GCTTCTCTTCCCCAG	55298
rs574480790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990964	ATAAGCCAGTTAATG[C/T]AGGAACAGAAAACCA	55298
rs574485850	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71979419	TTTCTCTCTCTCCTC[-/T]TTGTTCTCTCTTTTT	55298
rs574528312	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926927	TAAAATAAAATAAAA[G/T]AAAATAAAATAAAAT	55298
rs574552072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963491	TGGGCGTGGTGGCAC[A/G]TGCCTGTAATCCCAG	55298
rs574561197	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71977289	AGTGCCAAGCACCTG[A/T]GGACTGGAAAGGCAC	55298
rs574618004	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990470	TGGATTTGGTCATAG[C/T]TTGCCCGCACTTGCT	55298
rs574619132	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71976637	TGCTGGGGTTACAGG[C/T]GTGAGCCACGGCACC	55298
rs574688985	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992953	CAGTGTCATCCCCCA[A/G]GACCCCACCCCAAGA	55298
rs574717162	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933921	GCTTTTTTATTAAAT[G/T]TTTACGACATCCCCG	55298
rs574767209	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949347	TGCTTAGGCCTGGAA[A/G]GTCGACACTGCAGTG	55298
rs574780677	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937927	TCCTCAGAGAAAAAT[C/T]TGTAGGTAAAATAAA	55298
rs574827504	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992402	CAACATTTAATATTA[A/C]AAGTGTTTTGAGTCT	55298
rs574851495	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956624	GTGTAGCCTAGCGGC[C/T]ACCATAGGGCCATTT	55298
rs574983777	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71984019	TGTGGAAGATACAGG[A/T]TGTGGAGCCAGATGA	55298
rs575189072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995225	TCCCATTCTCTGCCT[A/G]TGTTGGGAAAGCCAT	55298
rs575360550	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989679	GGTTGCAAATTATCG[A/G]TCCTTGGAATTATTA	55298
rs575363078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938405	GCTCACCATAACCTC[C/T]GCCTCCTGGGTTCAA	55298
rs575408099	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981784	ACTTATCGGAATTTA[C/T]TGAGGACATATCATA	55298
rs575436982	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71971821	GGAGCTTTCTTGTAC[-/T]TTTTTTGTGGGTATG	55298
rs575439141	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71977756	TTCCTGACAGCTCCT[A/G]CCTCATCTTTCCACT	55298
rs575607139	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927958	GCCATCCTAGTTCCA[C/T]TCACCAGACAGATCC	55298
rs575616185	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945832	AAAAATGGGCAAAAG[A/G]CCAGGCCCAGTAGCT	55298
rs575658057	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931322	TTCATTTCCTGAGAA[A/G]AGGTATAATCTGTTG	55298
rs575673011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930983	GATTACAGGCATGCA[C/T]CACCACGCCCGGCTG	55298
rs575722648	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71980730	AACTGCTCTAAGCTG[C/T]ACTACCTATTATGGT	55298
rs575777836	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955163	CAAGTGCAGGGTAGG[C/T]ACCTGAGAGTGAGTG	55298
rs575930870	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996482	TATGATGGAGAGCCA[C/G]CCAGTGGGGCTGTCA	55298
rs576032111	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71978055	CTAAAGTAGAAACTG[-/A]AAAAAATTTTTTGTA	55298
rs576051170	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71934346	AAGTACATGCAAAAT[A/G]TGTCACAGGTGCTGT	55298
rs576059751	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71985954	AACAAAAAAAAAGGC[A/C]CTGGTTCCTTCAGGG	55298
rs576060819	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943817	CCCTCTAGGCAGGAG[A/G]AGCAGCATGTGCAAG	55298
rs576091001	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978307	TGCCCCTCCCCAGGA[A/G]CTGGGTCCTTCCACC	55298
rs576149335	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943302	TTGAGTAAATGGCAT[C/T]ACCATGGTACCATTA	55298
rs576196741	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71941857	ATGAGGTCAGGGAGT[C/T]TGGCAAGGTCAGATT	55298
rs576230666	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957928	AATAGTGAGAAAAAA[A/C]CTATTGATTTTATTT	55298
rs576384181	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993724	GAGAATGGAATTGCT[G/T]GGTCATTTGGTAATT	55298
rs576415035	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958659	TGAGCCCAGCAGTTC[A/G]AGGCTGCAGTTCATC	55298
rs576489595	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954281	AGGAAGACTGGTTTG[G/T]ATGTAACTTAAATAA	55298
rs576543421	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981014	CATGATATTTCGTTT[A/G]GATAGCACTGGTCTA	55298
rs576618651	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71984307	TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG	55298
rs576670679	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936838	AATGCTTTAATGCAG[A/G]GACTATTTTTCTCAT	55298
rs576673438	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937313	AAATATTTATTGAAC[C/T]TGAATTTTTATTTTT	55298
rs576681216	in-del	-/AGAT			intron-variant	RNF121	GRCh38.p7	11:71985747	ATTAGCTCCCATCAC[-/AGAT]AGAATAGTGGCTCCT	55298
rs576755477	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983470	CTCAGCAAATTTATA[A/G]TTTTCCAATAAACAA	55298
rs576784300	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71938474	ATAGGCATGTGCCCC[C/G]ACGCCTGGCTAATTT	55298
rs576826005	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961346	TGGGCAGATGGCTTC[A/G]GCTCAGGAGTTCAAG	55298
rs576892387	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71946653	GAGCATGAGGTTTTT[G/T]TTTTTTTTTTAGAGT	55298
rs576906714	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71995949	CCCTCTATCTGCCTC[C/T]CACCTTCTCTGCATT	55298
rs576957792	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71946117	CTCTGCCTTAAAAAA[-/G]AAAAGAAAAGAAAAG	55298
rs577057972	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939590	GGAAAAGCTAATTCT[A/G]TTTTAATACTGTTAT	55298
rs577097126	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71990902	CAGCCATAAAAAAAG[A/G]TAAAACCATGTGCGT	55298
rs577152857	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997848	TTCTCACTGCCTGAG[C/G]ACAGTGTCCCGCCAC	55298
rs577174446	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71989879	AAACCTGTGTTTGAC[-/A]AGCTGTTTCTGTAAA	55298
rs577235150	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71969452	AAGTTGACACTTTTT[A/T]TAGAAAGGTAAAAAT	55298
rs577357253	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955967	AGTCCTGGTAAATTT[A/G]TTTTTTGACTTAGCT	55298
rs577373430	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71985023	TCCTCCTAGGCTCAA[A/C]CAATTTTCCCATCTC	55298
rs577379065	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71992303	AACAGCCACTGTCAC[A/T]TACTGCTTTACCAAA	55298
rs577396739	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71941378	ATTCAGTAAACATTT[A/C]TTAAGTTTGTGGTCT	55298
rs577433389	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994032	TTTTTAGTAGAGACG[A/G]GGTTTCACTGTGTTA	55298
rs577439997	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71980013	TCCCCAAATTTAAAT[A/T]ATCTGCAGTTGTTTG	55298
rs577469936	snp	A/G/T			intron-variant	RNF121	GRCh38.p7	11:71991458	CTCTTAGGTGGGAGA[A/G/T]ATGGCTATTACAGTA	55298
rs577499108	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71941229	GTAGTTTAGGAGCGA[G/T]ATGATGCGGACCTGA	55298
rs577517788	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71934942	GTTCCAAATGCATTC[-/T]TTTTTTTTTTTTTTT	55298
rs577545463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71965922	ACCTGATTTTATTAA[A/G]TATTTCTCTGATTAT	55298
rs577547169	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950039	CACACACACAAAACT[C/T]GCACAAAAAACCCAA	55298
rs577571379	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956567	TGATATCGCTAGTTA[A/G]TAGCAGCAGGGCAAG	55298
rs577606131	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966379	AGTCAGATAGTTCTA[C/G]AAGACTTCAGAAGCA	55298
rs577633772	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949282	AATTAGCTGGGTGTG[A/G]TGGCACGTGCCTATA	55298
rs577635175	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973117	CTTGAATCCAAGAGG[C/T]GGAGGTTGTGGTGAG	55298
rs577697807	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954109	CCTTACCTAATTAGC[C/T]ACCTGAGCTTTGGAC	55298
rs577718414	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994362	GGAACCATAGTCTGG[C/T]GACAGAATGGCTTGC	55298
rs577737553	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967949	TTTGTAAGAGCTCTT[C/T]GTAGGTCAGGAATAA	55298
rs577752977	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958724	AAATAATATATGTAT[A/G]TGTACCTACAATGTG	55298
rs577775653	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71941445	GTGACTTCAGTGTCA[A/G]ACATTTTTCTAGGTC	55298
rs577796589	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929421	TGGGTGTCTTAGGGT[A/G]GGACCGAAGGGCTAA	55298
rs577902106	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931264	ATAGGAGTTAACTTT[A/G]TATGAAACCACTAGC	55298
rs577927113	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71988024	CATTCGACAAGATTT[C/T]TAAGGAAACAGTTCT	55298
rs578031164	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945610	TCTGTCTGTCATTTA[G/T]TGAACACATACAGTA	55298
rs578063475	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71981646	ATTGTTTTATGCCTT[C/T]AAAAAACTTCAGCTA	55298
rs578094449	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71967720	GCCACTGTGCCTGGC[A/G]GTAATAATTATCTTT	55298
rs745307870	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71942184	ATAATCCATCTGCCT[C/G]GACCTCCCAAAGTGC	55298
rs745353992	snp	C/T			upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997731	GTTCCCAGCTGTTCC[C/T]CTGCTGACATCCCTA	55298
rs745356715	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71987446	GCTGTTTTTCTCGTC[A/G]GTGTGTACTGTTCAT	55298
rs745388105	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71983324	ACCGTTTTGAGTATC[-/T]TATCTCCCTCACTAA	55298
rs745529973	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71935527	TTAACTGGAGTCATG[C/G]TATTTGTCTTTTCCA	55298
rs745551302	snp	C/T	1.64833e-05	0.00287078	intron-variant	RNF121	GRCh38.p7	11:71986992	TGCACTAACCTTCTC[C/T]CCTTTCCCCAGGTTG	55298
rs745589741	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963267	TGCTTTTAGTGTCAT[A/G]TCTAAGAATCCATTG	55298
rs745669645	snp	A/G	1.64743e-05	0.00287	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994838	GAACACGTATAGGCT[A/G]TCCTGCAATCATGTG	55298
rs745723660	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71981599	TGGAGAGAAGACTAG[A/C]GATGACTTCAAATTT	55298
rs745726166	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71975983	GAAACAACTCCAACC[A/G]TGTTTCTGCCTTGTA	55298
rs745760899	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71988720	CCAGCTACTCAGGAG[A/G]CTGAGGTGGGAGAAT	55298
rs745837665	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71943537	CTGTTCACTTGTTTA[C/T]TGATTGGTCACATAC	55298
rs745876094	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71973011	GACCAACATGGAGAA[A/G]CCTTGTCTCTACTAA	55298
rs745968605	snp	A/C/G	3.30127e-05	0.00406269	synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960861	GCTGCTCCTGGTGCA[A/C/G]TGGAAGCAGAGGCAC	55298
rs745982197	snp	A/G	1.64977e-05	0.00287203	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996271	TGGCAGCCTGTCATC[A/G]TTGGTGTAGTCCAAG	55298
rs746004604	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940338	CTAAATGTTTTTTTC[C/T]GGTAGAAAAAAACAA	55298
rs746040775	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71983771	GTTGCAGTGCAGTTG[G/T]TAAGTGCTATGACAG	55298
rs746098082	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978966	TCTTTAATGATTCCT[A/G]TTTGGACTTCTAGAA	55298
rs746124556	snp	C/G	0.00100553	0.0223999	intron-variant	RNF121	GRCh38.p7	11:71978068	TGAAAAAAATTTTTT[C/G]TATTTTTTTTTTTTA	55298
rs746174683	snp	C/G	0.000185822	0.00963724	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928564	GAGGCAAGATGGCAG[C/G]TGCTGCAGCCAGGAA	55298
rs746186345	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71991975	AAAAAAAAACCTAGC[C/T]GGGCGTGGTGGCACA	55298
rs746224448	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71934225	TCAAACTTCTGAAAC[A/G]TCTGTGTGCCAGGCA	55298
rs746290409	snp	C/T	1.66657e-05	0.00288662	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996157	GATCACTCCTGGCAG[C/T]TCTTGCACAGAGTCT	55298
rs746306784	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71991773	CTGGAGAAGTAGTGA[C/T]TAGACTAGAAAAAAG	55298
rs746471998	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976084	TCTGGATGACTCTTC[A/G]GATATCATTTATCTG	55298
rs746492154	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71974944	CAGAGTCTAACATTA[C/G]TCTTTAGCTCCTTCA	55298
rs746511310	snp	A/G	1.64751e-05	0.00287007	intron-variant	RNF121	GRCh38.p7	11:71957269	GAGCAATGGAGGTAA[A/G]TGTGGTAGTTCGGGC	55298
rs746562990	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71943742	GACTCCCTAGAAGTG[A/G]TACCATAGCTGAGTG	55298
rs746616687	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71987721	ATAGGAAAAGTTTGC[C/T]GACTCTTGGGCTAGA	55298
rs746773435	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997206	AGAGTGCGTATGCGT[A/G]TGTGTGTGTGTGTGT	55298
rs746862355	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71964554	CGATTTCGGCTCACT[A/G]CAGCCTCTACTTCTG	55298
rs746867519	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71957899	CCAATGAGGTGATAT[C/T]AACCTTAGAATTTAA	55298
rs746874319	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71951895	AAATGGTACAGCTGC[A/C]GTGGAAAACAGTTTG	55298
rs746917494	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976799	TTAAGCCATTCCTTC[C/T]CCATTCTATACTTTG	55298
rs746917639	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963472	ATAAAAATACAAAAA[C/T]AGCTGGGCGTGGTGG	55298
rs746977986	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933408	ATATTATTGCCTCAA[A/G]TGAATAATTTACCTC	55298
rs746991969	snp	C/T	6.60644e-05	0.00574698	intron-variant	RNF121	GRCh38.p7	11:71994689	TTCTCACATCTTTTC[C/T]TATCTTTCCTTCCTG	55298
rs747018887	snp	C/T			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962158	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	55298
rs747046461	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949187	CTTTGGCAGGCTGGG[A/G]TGAGCGGGTCACTTG	55298
rs747062188	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71992921	TTATTTAAACAACAC[A/G]GAAGTGCTCCCTGTC	55298
rs747071037	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71981949	GAAAATGCGTTTGGA[G/T]CACTAGAAAGCACTT	55298
rs747113117	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71940035	AGGGTATGGCATTTA[-/G]GGCTGATTCTTAAAA	55298
rs747173085	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961028	TATGTATGAATGATG[A/G]ATAGTGTATTGGCGA	55298
rs747206387	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927634	GAACACAAGCTAATT[C/T]TAATTCATAATAGTT	55298
rs747247994	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71941535	TAATGTGGTAAAGTA[G/T]ATAACAAATAAACAG	55298
rs747249542	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71956254	TCTGTAGATCAGATC[-/T]AAAGAACATTTTCAG	55298
rs747317165	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71984250	TTGAAAATATGTCTG[-/TT]TAATACAGAGGATTT	55298
rs747398553	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967749	TTTACTGCTATACCT[A/G]TACCCGTTACATACT	55298
rs747420472	snp	A/G	3.5108e-05	0.0041896	intron-variant	RNF121	GRCh38.p7	11:71982964	TTCCGAAGCTAATGG[A/G]TTGGAATGCATGGGA	55298
rs747449620	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71980191	AGTTGTGGGTTCCTA[G/T]GTAGTGAATTGTTAT	55298
rs747467128	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71994484	TTACATCTAACTTCC[C/G]AACTGTCTCTAGTCT	55298
rs747473068	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71981330	GCTGGGATTACAAGT[G/T]TGAGCCACCACGGCC	55298
rs747487239	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942339	GATTGTAGGAGGTGA[C/T]TCAGTGAGAGGGTTA	55298
rs747510704	snp	C/T	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987104	TTTGGTCTTAACTTA[C/T]TATTCAAGTGAGTAC	55298
rs747635558	snp	A/C	3.30721e-05	0.00406632	intron-variant	RNF121	GRCh38.p7	11:71994678	ACTTTGGCTGCTTCT[A/C]ACATCTTTTCCTATC	55298
rs747636641	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71978469	TAAACATTAATAAGA[A/C]ATTGCTTATAACCTT	55298
rs747638953	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71951548	GGAGGATTGCTTGAG[A/C]CCAGGGATTTGAGGC	55298
rs747648455	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71932963	TGGGCCTAGCCAGCT[C/G]AGCTCAGGTATTAAA	55298
rs747653905	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71947199	ATACTAACAATAATT[A/G]AATTTCTTACTTAAA	55298
rs747681181	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978256	TTCCCCTTTTATCAC[A/G]TGGTAGACTGTTCTG	55298
rs747698912	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71931569	ATGTAATTATGGGGT[C/G]TACTGTGTGTTATGC	55298
rs747728210	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949942	GGAGGCAGACGTTGC[A/G]GTGAGCCAAGATTGC	55298
rs747754046	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71990357	CAGAGTGAGGAAAAG[G/T]GGTAGGAGGGGATAC	55298
rs747806298	in-del	-/TTT			intron-variant	RNF121	GRCh38.p7	11:71984748	CACACCCGGCTAATT[-/TTT]TTTTTTTTTTTTTTT	55298
rs747860178	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71944904	TCCTAGCTGTATGCT[G/T]TGTTAAGTTTGGAAA	55298
rs747949909	snp	C/T	1.70171e-05	0.00291689	intron-variant	RNF121	GRCh38.p7	11:71960941	AGTCATCAAGAGACC[C/T]TTCCTAAGTATTCTA	55298
rs747958552	snp	C/G			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998035	ACTTTTTCCCCCCAC[C/G]CCCCTGTCAGGCTCA	55298
rs748117512	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71953118	GGCTCACTGCAGCCT[C/G]AAACTCCTGGGCTTA	55298
rs748149431	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71965503	CATCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT	55298
rs748193761	in-del	-/AAAAG			intron-variant	RNF121	GRCh38.p7	11:71946113	AAGACTCTGCCTTAA[-/AAAAG]AAAAGAAAAGAAAAG	55298
rs748236753	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951734	CATGAAAAGAAGTCC[A/G]ACGTCATTTAGCTGT	55298
rs748252591	snp	A/G	0.000247576	0.0111232	intron-variant	RNF121	GRCh38.p7	11:71995425	GCCCTGGCTCTCACC[A/G]TTTCCCTTGACCAGC	55298
rs748260731	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71993010	CTTTAATCTAGTACC[A/G]TTTAAGGCCAGGGAC	55298
rs748311006	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71951207	GAGCAAAACTCCGTC[-/AA]TCAAAAAAAAAAAAA	55298
rs748325130	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994912	CACACTGTAGTGAGA[A/G]AGAGAAAGAGGGTGG	55298
rs748383288	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930180	TTGATAGCTAGTGGT[C/G]TTTGTGATCTTGCAC	55298
rs748416545	snp	C/T			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962215	CCTTGTGATCCGCCT[C/T]GGCCTCCCAAAGTGC	55298
rs748464246	snp	A/G	8.24151e-05	0.00641878	intron-variant	RNF121	GRCh38.p7	11:71994865	TGTGTATCCTGCCTC[A/G]AGCTCCTGGGCCACA	55298
rs748592774	snp	A/C/G			intron-variant	RNF121	GRCh38.p7	11:71968687	TTATTTGTTCAGTCA[A/C/G]TAGATATTCGTTGAT	55298
rs748616567	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71937269	TCAGCACCTAATCTT[C/G]CACAGTGGCTAGCAT	55298
rs748681830	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954362	ACATTTGTAGTACTC[C/T]ATGAAGTGCTAATGA	55298
rs748704255	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71995148	TCTAATGGGATCCCT[C/G]AGTTTAGCATCATCC	55298
rs748715169	snp	C/G	1.64887e-05	0.00287125	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982852	TCTGGATCTTGTTCT[C/G]TGCTGTCACAGCCTT	55298
rs748768786	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982989	ATGGGAGGAGCATAG[A/G]TTTAGACTGAAAAAA	55298
rs748810534	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71965687	GCATACCTGTGCAAG[C/G]AGTTTTATAGAATGC	55298
rs748811900	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71988643	CTCTCAACTCTTAAA[-/A]AAAAAAAAAAAAGAA	55298
rs748830769	snp	C/G	1.65559e-05	0.00287709	intron-variant	RNF121	GRCh38.p7	11:71987148	TTTTGCTGGAGTTTG[C/G]GGAGGAGTGACTGTT	55298
rs748937106	snp	A/G	0.000193442	0.00983279	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928633	CTACAACTCTTTCGT[A/G]GAGGGAGCGGAATTT	55298
rs748991667	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71933198	AGCTTGGGAATTAAG[G/T]TAAAAAAGCACTTCA	55298
rs748992309	snp	C/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990637	TTTGGCATCTCCCTT[C/G]TCTTCTATGGCCTCT	55298
rs749062387	snp	A/G	1.66971e-05	0.00288934	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960758	CTTTCAGGGTCGAGC[A/G]CGCACGCATGCATGC	55298
rs749099774	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976309	TAACAGAGCAGAGAA[C/T]AGTAGACCTGCTGCC	55298
rs749108370	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71955341	TGATCACCTGGAGGT[C/T]TTATTAAAAGGCAGA	55298
rs749130093	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942039	CTGGGTTCGTGCCAT[C/T]CTCCTGCCTCAGCCT	55298
rs749198648	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985595	ATCACTGCTTGCCTG[A/G]CCACAGCAAGGAGGC	55298
rs749272222	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71955683	TTGGGACAATTAATA[C/G]ATAGGCTTGGTAAGA	55298
rs749365059	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71934128	GCTTCTTGGACTATT[C/G]CGATCTACACTGCTA	55298
rs749372463	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71938561	CGATCTCAGGTGATC[C/T]GCCTGCTTCGGCCTC	55298
rs749387570	snp	A/C/G			intron-variant	RNF121	GRCh38.p7	11:71982417	AAATGACATGGTGAA[A/C/G]ATTTCGTGTTCGAGA	55298
rs749410273	snp	A/C	1.64909e-05	0.00287144	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982824	AAGCTGCACTGGTGG[A/C]GGTTCCTAGTGATCT	55298
rs749434242	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961512	AGGCTGCAGTGAGTC[A/G]TGATCGTGCCATTGC	55298
rs749434440	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71952704	ATCCTAGCTACTCAG[C/G]AGGCTGAGGCGAGGG	55298
rs749502906	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71936686	GGCGTGAGCCACTGC[A/G]CCCGGCCTTTTTCAG	55298
rs749503394	in-del	-/TAA			intron-variant	RNF121	GRCh38.p7	11:71939306	AGCCTCACTGTTTGG[-/TAA]CTTAGGCACACTTAC	55298
rs749645354	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991478	CTATTACAGTAACAA[A/G]CACAGATAAAAATAA	55298
rs749664283	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71945153	CCACCACACTTGGCT[A/G]ATTTTTAAATTTTTT	55298
rs749667424	snp	C/T	9.62788e-05	0.00693759	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929087	TGGTGGAGGTGGAGG[C/T]TGGAGGTGGTGCTGC	55298
rs749761020	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971661	AAGGAAACCCAAAAG[A/G]CCATTAAGCATGAAA	55298
rs749886352	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969423	CAAAAGAAGAGTCCT[A/G]GAAGACCACTTATAA	55298
rs749916948	snp	A/G	0.000367721	0.0135545	intron-variant	RNF121	GRCh38.p7	11:71960899	CCTACAATGTAAGCC[A/G]CTTTGCCTCTTACTT	55298
rs749978838	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71956795	TCTCTTATTTCTTCT[G/T]CTGGATAATTCACAT	55298
rs750042598	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71937026	TCTGGAAATAATACA[A/G]TAGCCCCTATCAGTA	55298
rs750092412	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71951522	TCCCAGCTACTTGGG[C/T]GGCTGGGGTGGGAGG	55298
rs750206860	snp	A/G	4.95806e-05	0.00497874	intron-variant	RNF121	GRCh38.p7	11:71990730	GGGGTAAGTTCATCC[A/G]GGTTCTTAAATACTG	55298
rs750219758	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983891	CTTCCTATTCTTCTT[A/G]TGTTCTACTTTCCTG	55298
rs750281035	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958946	AGAACAAGAAACTTA[C/T]CTCTTGCTATCTTTA	55298
rs750324701	snp	C/G	5.3526e-05	0.00517302	utr-variant-3-prime, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995551	GGATGTTCAGCAATC[C/G]GTATCCTTTATTGGG	55298
rs750405545	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71957688	CTTTGAAGATGATTA[C/T]CATTAACATCATCAT	55298
rs750407679	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71971217	GGTCAAACCCTATCT[C/T]TACAAAAAATAAAAA	55298
rs750447584	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71968282	CCAGGCTGATCTCGA[A/T]CTCTGGACTTCAAGT	55298
rs750459975	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71941374	ATGTATTCAGTAAAC[A/C]TTTATTAAGTTTGTG	55298
rs750475798	snp	G/T	1.65244e-05	0.00287436	intron-variant	RNF121	GRCh38.p7	11:71957186	TTGGCAGGGACAGTT[G/T]TAAGACAGTAACGGA	55298
rs750650377	snp	A/G	1.70252e-05	0.00291759	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996358	CCCCACACGCCATGG[A/G]CCTCAGGGCACTCTC	55298
rs750667763	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966230	CTCCACGTTGGTCAG[A/G]CTGGTCTCGAATGCC	55298
rs750676003	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942035	CCTCCTGGGTTCGTG[C/T]CATTCTCCTGCCTCA	55298
rs750682676	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71978071	AAAAAATTTTTTGTA[-/TT]TTTTTTTTTTAAGAG	55298
rs750682747	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71954116	TAATTAGCTACCTGA[A/G]CTTTGGACAAGGTGC	55298
rs750690788	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71970604	GAGTTTAACGCTTCA[A/G]TAAACTATGATCACG	55298
rs750732255	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994363	GAACCATAGTCTGGC[A/G]ACAGAATGGCTTGCC	55298
rs750778348	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950142	GCTGAATTGTCTGAA[A/G]TGCTAGGTTGCTCAG	55298
rs750846267	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961762	ATCGATATGCTGTCT[A/G]TAGTAAATTCACTTT	55298
rs750908578	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929792	ACAAGGGGCCCCTCC[A/G]TTGAAGAGCCCACAG	55298
rs750967187	snp	A/G			upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928668	TTCCGGGTCAGCCTC[A/G]GTGCAGCTTGGGAAA	55298
rs750970841	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71974184	CTGACCTCGTGATCC[A/G]CCCTCCTCGGCCTCC	55298
rs751036545	snp	A/G	5.11697e-05	0.00505789	intron-variant	RNF121	GRCh38.p7	11:71960735	CTTGATTCACCCCAT[A/G]TGTTTGGCTTTCAGG	55298
rs751038246	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927156	ACAAGGTTGAGGTGG[A/G]AGAATTGCTTGAGCC	55298
rs751059038	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71990277	CACTATGTAGGTCCC[C/G]ATGAGCATAGGTCCT	55298
rs751072364	snp	A/T	4.54308e-05	0.00476585	stop-lost, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995524	ACTGCAAAGAGAAGG[A/T]AGACCTCAAGAGGAT	55298
rs751077424	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71959093	TGTGATATACAGATG[G/T]GAGGTTAATTGGCCA	55298
rs751106793	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951130	TCGGGACGCTGAGGT[A/G]GGAGAATCGCTTGAA	55298
rs751111590	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71974668	TTGTCAATTTCTGCC[-/A]ATAGTCAGAAGTTTT	55298
rs751127526	snp	G/T	8.94574e-05	0.00668736	intron-variant	RNF121	GRCh38.p7	11:71995395	CTTTCAAAGACTGTC[G/T]GGGGCTGGAGTGCCG	55298
rs751178048	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71938152	AGCCTCAACATTTTA[C/G]TCCCTGTTGCCCATA	55298
rs751236617	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71977786	TGAATTCCCATGTCC[A/G]TACTTGATGCTTTGT	55298
rs751243641	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71965255	ATGACTGCATAGTAA[-/TT]TTTTTTTTTTTTTTT	55298
rs751251017	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71983101	CGATTAAAAACCTCA[A/C]ATATTTCTGTATAGC	55298
rs751289660	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979283	GGACCTCCTTAGGGT[A/G]ACCTATTGAGTTGGA	55298
rs751289791	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965209	CTCAAATATCTATCC[A/G]TATTGGTGGGTATAT	55298
rs751292716	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71990509	TGGGCCTTCTCGCTT[G/T]GGGCCCTGCCTTGTG	55298
rs751379205	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933630	TAGTCCACTGATTGG[A/G]TGACCCCACTTCATG	55298
rs751415310	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71932769	TTTCTTTGTGTATAA[A/C]ATTTCCATTTTCAAA	55298
rs751485312	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71935932	GGCTCACTGCAGCCT[C/T]CGCCTCCTGGGTTCA	55298
rs751528410	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71960598	CTGTCTGTTAGGGTG[G/T]GTGTCCTAGCCCCTA	55298
rs751601971	snp	A/G/T			intron-variant	RNF121	GRCh38.p7	11:71987948	AGTTTCAAGAATGTC[A/G/T]CAGTCCAGATGTGTT	55298
rs751624761	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975703	TAAATGTTTATTAAA[C/T]GACTGCTTGACTGAC	55298
rs751625098	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71944299	GATTGTGCCACTGCA[C/T]TCCTGCCTGGGCAAC	55298
rs751636980	snp	C/G	9.57075e-05	0.00691698	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929047	GGGACTGCGGTGAGG[C/G]GGCGAGCCGTGAAGA	55298
rs751764809	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71986623	AAAATATAAAAATTA[A/G]CCGGGTGTGGTGGTG	55298
rs751772691	snp	C/G	3.29772e-05	0.00406048	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996249	CTGGCTTCGATACTT[C/G]GTAGCCTGGCAGCCT	55298
rs751814216	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982011	TCGTGTGTCTTGGAT[A/G]TGATATTGTCAGGCA	55298
rs751915657	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928079	CGTAGGGGTGGGACA[A/G]TGAATGGTGTATAAA	55298
rs751940875	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937181	CAGCACTTACCATGT[C/T]GTATTGTCTTTTCCA	55298
rs751960702	in-del	-/AATTA			intron-variant	RNF121	GRCh38.p7	11:71952841	AATACAATGTGGAAT[-/AATTA]AATCAAGCTAGTAAC	55298
rs751991383	in-del	-/TG	1.65266e-05	0.00287455	intron-variant	RNF121	GRCh38.p7	11:71986968	TAAGGCCAGAATCTC[-/TG]TGTCAGCTGCACTAA	55298
rs752014499	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963819	GTCAGAAATCAATTG[A/G]TCAAAGATATGTTGG	55298
rs752046995	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71949692	TGACAGAGTAAGACT[-/C]CCATCTCAAAACACA	55298
rs752131230	in-del	-/CTTC			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997172	CACTCTGCCACATCA[-/CTTC]CTTCTTGAAAGCCTA	55298
rs752135218	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71962852	CCTCCACATTCTTAT[A/C]AAGACTTCTTACTTC	55298
rs752239325	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71992486	TGACAGAAATATGAC[A/G]CAGGAACTGAACTCT	55298
rs752240382	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71948647	ATCTACTTTCACTTC[A/G]CTGCCCAAAGTGTGC	55298
rs752257957	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71991342	TAACATTCATTCAGT[A/G]GATACTTTTTAATGC	55298
rs752274898	snp	C/G	1.75702e-05	0.00296392	intron-variant	RNF121	GRCh38.p7	11:71995392	AACCTTTCAAAGACT[C/G]TCTGGGGCTGGAGTG	55298
rs752293937	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71960527	TTAGCTCTAATTCCA[A/G]TATCTAGGCTTGGTT	55298
rs752296904	in-del	-/TTC			intron-variant	RNF121	GRCh38.p7	11:71934939	AGTGTTCCAAATGCA[-/TTC]TTTTTTTTTTTTTTT	55298
rs752317937	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71959341	ACAGTGAACACCTTT[A/T]TACTTACCACCTGGG	55298
rs752371008	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71976218	ATGGCCTGCTGTCTT[-/A]ATGGCCATGCTTATT	55298
rs752432768	snp	C/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994813	ACGTCAGTGAAGAGG[C/G]GATCATTGAGAACAC	55298
rs752449405	snp	C/T	3.49357e-05	0.00417931	intron-variant	RNF121	GRCh38.p7	11:71982735	GGGAGCTGGCCAGAG[C/T]TGAAGTGCTTGTGTT	55298
rs752485129	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71970591	GCTTGGGCCCAGGAG[-/T]TTTAACGCTTCAGTA	55298
rs752604804	snp	C/T	1.68349e-05	0.00290123	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982906	AACCTCTAGTACAGA[C/T]AACCCCAAGGTGAGA	55298
rs752610202	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71979650	TGCTTCTCTCCTCAC[C/T]CAGAATGTACAGAGC	55298
rs752681788	in-del	-/TAAA			intron-variant	RNF121	GRCh38.p7	11:71953397	TCTCTGTAAAGTTGT[-/TAAA]TAAAGAGTCAAGTGT	55298
rs752687026	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933927	TTATTAAATGTTTAC[A/G]ACATCCCCGTGAGAA	55298
rs752696037	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71995800	ACTTGTGTCAGCCTC[A/G]GGCTGTGTTATCTTA	55298
rs752754206	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71932306	TGGAGTTAACCCCAT[C/T]TTATAAATGAAACTG	55298
rs752783188	snp	C/T	1.65499e-05	0.00287657	intron-variant	RNF121	GRCh38.p7	11:71990589	TAGCTCTAATGCTTC[C/T]CTTGCAGGATCAAAC	55298
rs752840273	snp	C/G	3.29478e-05	0.00405867	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987085	GGCTGTCATGTTTAC[C/G]CTCTTTGGTCTTAAC	55298
rs752846174	in-del	-/CCC			intron-variant	RNF121	GRCh38.p7	11:71992876	TTTATTGTTTTGCTG[-/CCC]TTTATAAAAGTAGTA	55298
rs752894615	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71964196	CTTTCATCAATGTTT[C/T]GTAGTTTTCAATGTA	55298
rs752991704	in-del	-/CA			intron-variant	RNF121	GRCh38.p7	11:71951221	CTCAAAAAAAAAAAA[-/CA]ATGCAATAATGAAAG	55298
rs752995345	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971584	GAGAAACTCCTACAA[A/G]TCAACAAAAGACAGC	55298
rs753052413	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71984640	CTCTGTCACCCAGGC[A/T]GGAGTGCAGTTCACT	55298
rs753054025	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960813	GCATGCTGAAATGGT[C/T]CTCATCCTCATCGCA	55298
rs753070867	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71983207	CATTTTAAATGTTTT[C/G]TTCTATGAACCCTTC	55298
rs753085689	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71971811	CAAAGGCTGTAGGAG[A/C]TTTCTTGTACTTTTT	55298
rs753151310	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71953824	TTTGGGGGGACAGGA[A/G]ACCTGTTTGTGGGGA	55298
rs753277810	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71952312	TAGTGGTTGCCTTGG[G/T]CTGCAGGGAACATGG	55298
rs753372984	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71935496	GTACATTTGGGTCTT[C/G]CTTTCCGGAGGTGAT	55298
rs753391519	snp	G/T	1.75529e-05	0.00296246	intron-variant	RNF121	GRCh38.p7	11:71982712	GGGACTGTGGACAGA[G/T]CTGCAGAGGGAGCTG	55298
rs753461296	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71979953	AACCTTCCAGCCCTT[C/G]TTTCCATATGCCACC	55298
rs753484509	snp	A/G	1.6591e-05	0.00288015	intron-variant	RNF121	GRCh38.p7	11:71990762	TTCTTGACACCTCCA[A/G]ATTGCTCAAGTTGAT	55298
rs753732009	snp	C/G/T			intron-variant	RNF121	GRCh38.p7	11:71969176	ACAGACGTGAGCCAC[C/G/T]GTGCCTGGCCCCTCT	55298
rs753748023	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71968350	CAGGTGTGAGCCACT[G/T]CCCCCAGCCCAATTT	55298
rs753759759	snp	C/T	1.6821e-05	0.00290004	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996344	CAGTGGAAAACCCAC[C/T]CCACACGCCATGGAC	55298
rs753762353	snp	C/T	1.64846e-05	0.0028709	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996226	GTCATGTATGGGCAA[C/T]TGCTGGACTGGCTTC	55298
rs753844508	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983550	ATTTTATTCAAATTC[A/G]TTTCTCATTTGATCC	55298
rs753926786	in-del	-/TA			intron-variant	RNF121	GRCh38.p7	11:71968669	TTATTGAGTACTGTC[-/TA]TTTATTTGTTCAGTC	55298
rs753947846	snp	G/T			upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997734	CCCAGCTGTTCCCCT[G/T]CTGACATCCCTAGGA	55298
rs753961621	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71933453	TTGCTCTTGTTAAAA[G/T]AGAAGACTGGACTAG	55298
rs754042130	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997082	GGCAATTGTTGGCAG[C/T]CATGACTGACGGCCC	55298
rs754080913	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71973964	TGTTTGTTTTTGAGA[C/T]GGAGTCTTGCTCTTT	55298
rs754087992	snp	G/T			intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978115	CGTGTTGCCCAGGCT[G/T]GTCTCAAGCTCCTGG	55298
rs754090495	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71932501	CTTTAAAATTGTATC[A/G]TCTTAATCATCTCAT	55298
rs754117227	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71964225	TACAAGTCTTGCACC[G/T]CCTTTGTTAAACTTA	55298
rs754122863	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71995780	CCATTGTCACGGATA[C/G]ATAGACTTGTGTCAG	55298
rs754170492	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71986460	GAATCTTTTCCTTGG[G/T]CTGAAACCATGAAAA	55298
rs754216475	snp	A/C	1.6473e-05	0.00286988	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994761	AAACATCTTTCAGAC[A/C]GTGTGTGTGCTGTGT	55298
rs754322735	snp	G/T	1.72698e-05	0.00293847	intron-variant	RNF121	GRCh38.p7	11:71960710	CCCTTTATCACTACA[G/T]CATCCCTGACTTGAT	55298
rs754359425	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927397	GCGTGGTGGCGCGTA[C/T]GTAGTCCCAGCTATT	55298
rs754450762	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71959144	AATCTAAGTTTCGAA[A/C]TCCCAATCCTATTCT	55298
rs754575280	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971483	GATTTCTGTTCTGTT[A/G]AAGATATGATAGGCA	55298
rs754578761	snp	A/G	0.000192623	0.00981194	utr-variant-5-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929091	GGAGGTGGAGGTTGG[A/G]GGTGGTGCTGCTGGG	55298
rs754591787	snp	A/G	1.65913e-05	0.00288017	intron-variant	RNF121	GRCh38.p7	11:71990763	TCTTGACACCTCCAA[A/G]TTGCTCAAGTTGATG	55298
rs754611342	snp	A/G	3.29451e-05	0.00405851	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994800	CAGATCTTTGTGGAC[A/G]TCAGTGAAGAGGGGA	55298
rs754649784	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71957851	TAAAAGGGTTTCAGA[G/T]TGCCTGCCCCACGAA	55298
rs754654677	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983112	CTCAAATATTTCTGT[A/G]TAGCTTACTTTATGG	55298
rs754708390	snp	A/C	1.64917e-05	0.00287151	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960843	AACCTTGGTGGTGGC[A/C]CAGCTGCTCCTGGTG	55298
rs754730402	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71954131	GCTTTGGACAAGGTG[C/G]CTTCAGACTGAGTTA	55298
rs754748369	snp	A/C	1.64846e-05	0.0028709	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996238	CAACTGCTGGACTGG[A/C]TTCGATACTTGGTAG	55298
rs754756205	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963789	CATTGGATGGTCGTG[A/G]CATGTCACGACCTTG	55298
rs754771936	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71933652	CACTTCATGTTCCCT[C/T]AGCCCGCTTGTACTT	55298
rs754813707	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71965505	CCACCTCGGCCTCCC[-/A]AAAGTGCTGGGATTA	55298
rs754880191	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933734	TAAGCTTCGTGAGAG[A/G]GCAGAGTCCAAGTGT	55298
rs754939173	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71978392	TGGCCTGGGGACCTG[A/C]AAATGGCCTCAAATC	55298
rs754963959	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71991200	TAACAAACCTGCACA[G/T]GTACCCTCTGAATCT	55298
rs755063989	snp	G/T	3.43696e-05	0.00414531	intron-variant	RNF121	GRCh38.p7	11:71982940	TAAGTAGTGGGAAGA[G/T]CCCAGGTTTTCCGAA	55298
rs755122639	snp	A/G			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962159	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	55298
rs755137459	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71944643	GTGCTCCTGTGGAGG[G/T]CATTGTGTAGTCTAC	55298
rs755177102	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71986626	ATATAAAAATTAGCC[A/G]GGTGTGGTGGTGGGC	55298
rs755305551	snp	C/G	1.64754e-05	0.00287009	intron-variant, missense, utr-variant-5-prime	RNF121	GRCh38.p7	11:71957235	TCTACAGGTTGATAT[C/G]TCAGATCTCTCTCCA	55298
rs755313221	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938212	CATTTAGTGCCCTGC[A/G]AACAGTCTTTTCTCC	55298
rs755318917	snp	A/G	3.29478e-05	0.00405867	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987077	GGCTACATGGCTGTC[A/G]TGTTTACCCTCTTTG	55298
rs755332974	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997281	CTGTGTCAGATGATA[C/T]GTCCTTGAAGCTGGC	55298
rs755367164	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71937213	TAGGCAGGGAACTCC[A/T]TGAGGGGACTGCACC	55298
rs755418582	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951711	GATACACAAATGGCC[A/G]AAGAACACATGAAAA	55298
rs755419082	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71967180	CGGCCAATATTTGTG[-/T]TTTTTTAAATAACAT	55298
rs755439812	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71952175	ATGCTACAAAGTGGA[C/T]GAACCTTGAAAGAAT	55298
rs755464935	in-del	-/GC	1.64893e-05	0.0028713	intron-variant	RNF121	GRCh38.p7	11:71994704	CTATCTTTCCTTCCT[-/GC]TATTCTCCTTCAGTT	55298
rs755487650	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71994536	CAGCAAAGATGAGGT[A/C]GATTTGACTTGTAAA	55298
rs755529478	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934011	TACTGTTTCTAATTA[C/T]TTCCGGGCTTTGTTG	55298
rs755540825	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971597	AAATCAACAAAAGAC[A/G]GCAACTCCAATAGAA	55298
rs755568908	in-del	-/ATAAAC			intron-variant	RNF121	GRCh38.p7	11:71955061	ATGGGATGGAAACAA[-/ATAAAC]ATAAACAGGGCCAGG	55298
rs755726071	snp	A/G	3.29739e-05	0.00406028	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990611	GGATCAAACCAGAAG[A/G]TGCCATGGACTTTGG	55298
rs755799879	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71972693	CACTTGTAACAACCA[C/G]ATGTCTCCAGACTGC	55298
rs755855216	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71941767	CAAATTAATGGGAAT[A/G]AACAAGGCATGTCCT	55298
rs755855569	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71956633	AGCGGCTACCATAGG[A/G]CCATTTAGAGTCACA	55298
rs755982572	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71966220	GACAGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT	55298
rs756046110	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71935485	ATTTCCATTATGTAC[A/G]TTTGGGTCTTCCTTT	55298
rs756064171	snp	G/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998041	TCCCCCCACCCCCCT[G/T]TCAGGCTCAGGTGAG	55298
rs756070327	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978386	TGGAGATGGCCTGGG[A/G]ACCTGAAAATGGCCT	55298
rs756071313	snp	A/G	4.94743e-05	0.0049734	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960826	GTCCTCATCCTCATC[A/G]CAACCTTGGTGGTGG	55298
rs756081951	snp	A/G	6.63592e-05	0.00575979	intron-variant	RNF121	GRCh38.p7	11:71995566	CGTATCCTTTATTGG[A/G]GTCGTTGTTGGGAGT	55298
rs756120070	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71979757	GAAAGAGGATCTTAG[C/T]GCAGGCTGGTTGTTT	55298
rs756221573	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71952396	CAACTTGGTGGTGAT[A/G]GTGGCACAACTTTGT	55298
rs756228456	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71964150	GTACCTGAACACAGG[A/G]TATCTTTTCATTTAT	55298
rs756243507	snp	A/G	1.70807e-05	0.00292234	intron-variant	RNF121	GRCh38.p7	11:71982931	GTGAGAGTTTAAGTA[A/G]TGGGAAGAGCCCAGG	55298
rs756254804	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71995848	TAGAGAAGGTGTTAC[A/G]GGAGGCCCTCCCTGC	55298
rs756280022	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963123	GACCATTATCAGATA[C/T]ATGATTTTAAAATAT	55298
rs756346458	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71965256	TGACTGCATAGTAAT[-/T]TTTTTTTTTTTTTTT	55298
rs756351186	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976659	CACGGCACCTGGCCC[A/G]TTCTGGGTATATTCT	55298
rs756422617	snp	A/G	1.65051e-05	0.00287267	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982811	CTATTTCACAGTGAA[A/G]CTGCACTGGTGGAGG	55298
rs756488942	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71971608	AGACAGCAACTCCAA[C/T]AGAAAAACAGGCCAG	55298
rs756508723	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983341	ATCTCCCTCACTAAA[C/T]TCTAACTCTGGGATC	55298
rs756583833	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71972010	GGGAGTAAATAGGTA[A/C]AATGTGACGGATGCA	55298
rs756590033	snp	A/T	4.96184e-05	0.00498063	intron-variant	RNF121	GRCh38.p7	11:71957188	GGCAGGGACAGTTTT[A/T]AGACAGTAACGGATT	55298
rs756612232	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71939951	GTTATAAATTACGTA[C/G]AAGATGCCACAAGTG	55298
rs756665035	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982251	TGAGGCAAGAGAATC[A/G]CTTAAACCTGGGAGG	55298
rs756667303	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953842	CTGTTTGTGGGGATA[C/T]GTTAGTGAGTCCCTG	55298
rs756698844	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71965019	ATGTTTATTTGTTAT[-/A]AAAAAAATTTGAACA	55298
rs756782139	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71935503	TGGGTCTTCCTTTCC[A/G]GAGGTGATTTAACTG	55298
rs756824488	in-del	-/CT	1.70148e-05	0.00291669	intron-variant	RNF121	GRCh38.p7	11:71995416	GGAGTGCCGCCCTGG[-/CT]CTCTCACCATTTCCC	55298
rs756847166	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967536	TGTATTTTTAGTACA[A/G]ATGTATTTTAGTACA	55298
rs756898594	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71979993	TCATGAGTTGGGTTG[C/T]GTTTTCCCCAAATTT	55298
rs756950075	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71944477	TCCAAATTTATCTAA[C/T]TCTAAAATGCACATA	55298
rs756951017	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71992694	TTCAAAGCTGAGATT[G/T]CTGATTCGGCAACTG	55298
rs756997951	in-del	-/AGAAT			intron-variant	RNF121	GRCh38.p7	11:71943790	TAACCAGCTAAAGAA[-/AGAAT]AGAAGAGCCCTCTAG	55298
rs757179442	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71986957	ATCAGGACCATTAAG[G/T]CCAGAATCTCTGTGT	55298
rs757204981	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71956824	ATCTCCTCCATAAAG[C/G]CTTCCCTAGTCTAAA	55298
rs757210628	snp	A/G	1.75059e-05	0.00295849	intron-variant	RNF121	GRCh38.p7	11:71995397	TTCAAAGACTGTCTG[A/G]GGCTGGAGTGCCGCC	55298
rs757261601	snp	A/G	0.000395283	0.0140529	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994829	GATCATTGAGAACAC[A/G]TATAGGCTGTCCTGC	55298
rs757296359	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71968396	GGCTAAGTACTCTAT[G/T]GTTTGCTATTCTGTT	55298
rs757360191	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954095	CCTTATCTTGAGAGC[C/T]TTACCTAATTAGCTA	55298
rs757397064	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71993697	TAGTTTCATATCTTT[C/T]GGGTTTATACCGAGA	55298
rs757404626	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71952759	GGTTGAGTGAGCTGA[C/T]ATCGTGCCACTGCAC	55298
rs757471299	snp	C/T	1.64961e-05	0.00287189	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996267	AGCCTGGCAGCCTGT[C/T]ATCATTGGTGTAGTC	55298
rs757471377	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938956	GTCGCCCAGGCTGGA[A/G]TGCAATGGTGTGATC	55298
rs757509828	snp	A/G			intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978137	AGCTCCTGGGCTCAA[A/G]CGATCCATCTGCCTC	55298
rs757517118	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950765	TCACACCATTCCCCT[A/G]CCTCAGCCTCCCCAG	55298
rs757558784	snp	C/T			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996530	AAAAGAAAACTATTT[C/T]GATGAATATATTTAA	55298
rs757577750	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71961730	TTGGCAGATTGGTTT[C/T]AAAAATCCCCTCATT	55298
rs757616109	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987105	TTGGTCTTAACTTAT[C/T]ATTCAAGTGAGTACC	55298
rs757644546	snp	A/C	0.00138518	0.0262806	upstream-variant-2KB, nc-transcript-variant	RNF121, LOC100133315	GRCh38.p7	11:71928411	GCCTCGGATCTCGGA[A/C]CACCAAACCTATTCT	55298
rs757697638	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972808	GCTATGAGACTGATG[A/G]TGAGCAGTATGCCAG	55298
rs757730099	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985058	TCTGTAGTAGCTGGG[A/G]CTACAGGCATGCTCC	55298
rs757750181	snp	C/G			upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928474	TGACCCCGAGAGCTA[C/G]TCTTCCGTCTTCCGT	55298
rs757761064	in-del	-/TTTG			intron-variant	RNF121	GRCh38.p7	11:71973938	CCCTGTATTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT	55298
rs757767187	snp	A/C	1.65029e-05	0.00287248	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990601	TTCCCTTGCAGGATC[A/C]AACCAGAAGATGCCA	55298
rs757803530	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71941307	TGTTAAATAGCAGTG[C/T]TTTCACTTATTTATG	55298
rs757824081	snp	C/G	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994821	GAAGAGGGGATCATT[C/G]AGAACACGTATAGGC	55298
rs757826941	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971910	TGTGACACATCCTAA[A/G]GGGATATGTAAGAGG	55298
rs757857034	in-del	-/CATTT			intron-variant	RNF121	GRCh38.p7	11:71992377	ATGTGTAAAGCTACA[-/CATTT]CATTTCAACATTTAA	55298
rs757933676	in-del	-/GA			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927617	TTAAAAATGGACTGG[-/GA]GAACACAAGCTAATT	55298
rs757981745	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71981915	TACTCTAGATAAGCA[C/T]TATAATAATGTTAGA	55298
rs757991601	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71956881	AAAGGCAAGGCACCT[C/G]TTTGTTCTATAGCTA	55298
rs757993567	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969507	TCTTTTTTTTGGCTA[A/G]GTTTGTGTTAGGCAT	55298
rs758009015	snp	A/C	1.70971e-05	0.00292374	intron-variant	RNF121	GRCh38.p7	11:71960732	TGACTTGATTCACCC[A/C]ATGTGTTTGGCTTTC	55298
rs758117187	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981024	CGTTTGGATAGCACT[A/G]GTCTAGAAATCCCTA	55298
rs758118330	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968500	TTTAGGTAATAGCCA[C/T]AGCTACCAATTTTAC	55298
rs758154577	snp	C/T	1.70743e-05	0.00292179	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982768	TGTTTCAGATGGTGA[C/T]CCTCTTTCAGATGTG	55298
rs758308199	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71983936	GCCTTCTGGAGTTTC[A/T]TTGTATAAGGTAAAA	55298
rs758329892	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71944646	CTCCTGTGGAGGGCA[C/T]TGTGTAGTCTACTAA	55298
rs758329942	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71990155	CTGGCATGCCCTTTC[C/T]TCCTTATGGATGGCT	55298
rs758348530	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71988859	ATCCTATTTTATATA[G/T]TGAGAGTGCACTCAT	55298
rs758354237	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929476	TGAATTTCTTCAGGG[A/G]AAGGCTGGGCTTCTA	55298
rs758407027	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71959906	CTCTCAAAGTGCTGG[G/T]ATTACAGGTGTGAGC	55298
rs758424666	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71942079	CTGGGACTACAGGTG[C/G]CTGCCACCACGCCCA	55298
rs758444423	snp	G/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928804	ATTGGTTAAATAGTT[G/T]CACTGAAAATAATGC	55298
rs758521085	snp	C/T	1.65463e-05	0.00287626	intron-variant	RNF121	GRCh38.p7	11:71990590	AGCTCTAATGCTTCC[C/T]TTGCAGGATCAAACC	55298
rs758528268	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71973045	TACACTGTTAGCCGG[A/T]CATGGTGGTGCATGC	55298
rs758531858	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71940385	TACCCTCTCATGGAT[A/G]TGGCTAGGGAAGACT	55298
rs758564695	snp	A/G			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71997971	CTGTTCCCCTCCTCA[A/G]AGAGGGGAATGGGGC	55298
rs758635655	in-del	-/A	1.75468e-05	0.00296194	intron-variant	RNF121	GRCh38.p7	11:71982718	TGGACAGAGCTGCAG[-/A]AGGGAGCTGGCCAGA	55298
rs758689981	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71985220	GTGTGAGCCATTGTG[C/G]CTGCCCTCAAAGCAC	55298
rs758718037	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71935557	ACCAGACTGTGTTCT[C/T]CTCGAAAGGAAGGCC	55298
rs758796654	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71962753	TGGTAACTCTGTGTT[G/T]AATGTTTTGAGGAAC	55298
rs758815885	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71953892	AAATGTAGCAGTCAA[C/G]TTCTCATAATTTTTC	55298
rs758821699	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71992838	TAAATATTTCTATTT[G/T]TTTTTTCAGAATGGA	55298
rs758839540	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71994467	CCAGTTTATAGGTTC[C/T]GTTACATCTAACTTC	55298
rs758850843	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71944932	AAAGTATTTACTGCT[-/G]GCTATTAAAGATCAA	55298
rs758858539	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929850	CTAGTCATTGCATTA[C/G]AGATATAATGGTGGC	55298
rs758924019	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996122	TGGGGCAGACCCAGG[A/G]AGCCCCACCACCCAT	55298
rs758925134	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71973627	CCCCGTCTCTACTAA[C/T]AATACAAAAATTAGC	55298
rs758925411	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987089	GTCATGTTTACCCTC[C/T]TTGGTCTTAACTTAT	55298
rs759013744	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71974188	CCTCGTGATCCACCC[G/T]CCTCGGCCTCCCAAA	55298
rs759083300	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71940745	CCAGACATGGGAACA[A/G]ATGGTTGTAGTATAG	55298
rs759092766	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71972541	CTCTGTTCTCCTAGA[C/G]CAAGGTTTCTCAACA	55298
rs759104522	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927191	AGATGAGACTACAGT[A/G]AGCAGTTATCACGCC	55298
rs759110278	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71985819	TGGTTTGGCCAAGCA[C/T]CAGTGGCTTATGCCT	55298
rs759128792	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71984520	CTCCTGACCTCATGA[C/T]CTGCCTGCCTCAACC	55298
rs759139637	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71967639	TGTTGGCCAGGATAG[G/T]CTCGATCTCCTGACC	55298
rs759143539	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940806	CAAAGGAGGGAGTGA[C/T]TAACTCTGCTTCGGG	55298
rs759214575	snp	A/C			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997571	CCCGTCTGAATAAAG[A/C]TCCATGAGCTGGGTT	55298
rs759265137	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979442	CTCTTTTTTTCTCAC[A/G]CACAGTCTTTTTCTT	55298
rs759316236	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71952301	AGAATGTAAATTAGT[A/G]GTTGCCTTGGGCTGC	55298
rs759332620	snp	C/G	1.75431e-05	0.00296163	intron-variant	RNF121	GRCh38.p7	11:71982720	GGACAGAGCTGCAGA[C/G]GGAGCTGGCCAGAGC	55298
rs759338049	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71935153	GCTCAGACTGGTCTC[A/G]AACTCCTGGACTCAA	55298
rs759338244	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980424	CGATCTCAGCTTGCC[A/G]CAACCTCCACCTCCC	55298
rs759345950	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950789	TCCCCAGTAGCTGGG[A/G]CTACAGGCAGCATCT	55298
rs759346532	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71941932	GCGTGTAATGAGAAT[-/TT]TTTTTTTTTTTTTTT	55298
rs759423940	snp	A/T	0.000111439	0.00746373	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929173	CCTGAGACTGAGGGG[A/T]GGGGCAGTGAGGTAT	55298
rs759464354	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949433	AAAAAAACAAAAACA[A/G]GCCAGGCATGGTGGC	55298
rs759492115	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71948242	GGTTTTTGGCCAGGT[G/T]CGGTGGCTCACGCCT	55298
rs759533522	snp	C/T	3.36814e-05	0.0041036	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996346	GTGGAAAACCCACCC[C/T]ACACGCCATGGACCT	55298
rs759600501	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71958498	AACTGTCTTTAATAG[G/T]CAAGGTATATTGAGA	55298
rs759646463	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976646	TACAGGCGTGAGCCA[C/T]GGCACCTGGCCCATT	55298
rs759776357	snp	C/T	3.32618e-05	0.00407797	intron-variant	RNF121	GRCh38.p7	11:71990577	GGTGGGTCTTTCTAG[C/T]TCTAATGCTTCCCTT	55298
rs759779524	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71957439	CTCTTAGTCTTGAAT[A/G]TGTAAGCAGATGATT	55298
rs759786162	snp	C/T	1.65056e-05	0.00287272	intron-variant	RNF121	GRCh38.p7	11:71994897	CTCTCCTGCAATCTG[C/T]ACACTGTAGTGAGAG	55298
rs759814234	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71950470	GCACCTGTAATCCCA[G/T]CTACTGGGGAGGCTG	55298
rs759815502	in-del	-/GAATG			intron-variant	RNF121	GRCh38.p7	11:71988425	CAAATTTAAGATAAT[-/GAATG]GGATGATCACTGGCC	55298
rs759903386	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71955839	AGTATCTGACCTCTA[C/T]CCTTCTGGGAGATGA	55298
rs759969079	snp	A/G	1.65007e-05	0.00287229	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960796	CGTGGCCATGAAGCT[A/G]TGCATGCTGAAATGG	55298
rs759977715	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71960738	GATTCACCCCATGTG[-/T]TTGGCTTTCAGGGTC	55298
rs760017952	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990382	GGATACTGTAGCTTG[A/G]TCTTCACAGCCTACA	55298
rs760047650	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71964835	ATGTTGTGGAGGGGA[A/T]GTTTGTGATTTTTTA	55298
rs760069025	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71932108	TCTAGAAGTTGAGAC[A/G]TAATTTAGGCTTTCC	55298
rs760093454	snp	A/T	1.72083e-05	0.00293323	intron-variant	RNF121	GRCh38.p7	11:71960719	ACTACAGCATCCCTG[A/T]CTTGATTCACCCCAT	55298
rs760102686	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71977903	AGTGTGCAAATTAGT[C/G]AACCAAATGTGTCTC	55298
rs760124488	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71962324	CTGCAGTAATTTTCA[A/G]TAAGAACTTTTTCCT	55298
rs760177041	snp	A/C	1.66045e-05	0.00288132	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982884	GTTACCTTCCGAGCC[A/C]CCCGAAAACCTCTAG	55298
rs760179878	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983721	GCCCTCAAGGAGTAC[C/T]CTGTTTAATGGAGGA	55298
rs760246595	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71986505	GGGTGTGGTGGCTCA[C/T]GCCTATAATCCAAAC	55298
rs760280940	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71986246	TGTATTCAGACTAAC[C/T]GGGCCCAGGTACAAA	55298
rs760284394	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929517	GGACTCTGTCTAAGC[C/G]TAGGGTGGGGGTTGG	55298
rs760298499	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71943226	TGGATTGGATATGTG[A/C]TGTAAGGGAAAGAAA	55298
rs760303990	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71973911	AAATTTTGAAAAATA[C/G]AAAAAACAAAAGCCC	55298
rs760449561	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71937493	ATTTTTGTATTTGAA[A/G]ATGAATCTTAAATCT	55298
rs760476299	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71969056	ATGCCCGGCTAATTT[C/T]TGTATTTTTTAGTAG	55298
rs760485369	snp	A/G	3.29848e-05	0.00406095	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996211	TGGGAGAGGCCTCAC[A/G]TCATGTATGGGCAAC	55298
rs760497906	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951015	GGATCACCTGAGGTC[A/G]GCAGTTTGAGACCAG	55298
rs760520410	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71980575	TGGTCTTAAACTCCT[C/G]ACCTAAGGTGATCTA	55298
rs760577745	snp	C/G	9.6567e-05	0.00694796	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929033	AGCTGGCTCGCGCGG[C/G]GACTGCGGTGAGGGG	55298
rs760615972	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927393	CCAGGCGTGGTGGCG[C/T]GTACGTAGTCCCAGC	55298
rs760626788	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965035	AAAAAAATTTGAACA[A/G]TGTAACAGTATGTGA	55298
rs760676417	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933398	TGAGGTATTAATATT[A/G]TTGCCTCAAGTGAAT	55298
rs760685269	in-del	-/GCCTTCTGACCTTC	0.000187776	0.00968776	upstream-variant-2KB	RNF121	GRCh38.p7	11:71928439	TCTCCCGCCAATTCG[-/GCCTTCTGACCTTC]GCCTTCTGACCCCGA	55298
rs760703019	snp	A/G	3.3983e-05	0.00412193	intron-variant	RNF121	GRCh38.p7	11:71957304	CAGTCTAGGAACTGC[A/G]GGTTAACCCAGCTTA	55298
rs760721586	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71948328	CGAGACCAGCCTTGT[C/G]AACGTGGTGAAACCC	55298
rs760721983	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994031	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	55298
rs760765831	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978845	TTTTCAGAGTTAAAC[A/G]ATCTGCCTAAGTTAA	55298
rs760803119	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71992108	GACGTTGTCTCTAAA[G/T]AAGTAAAAATTCACA	55298
rs760804009	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71953028	AGATTTTGTACAGAA[G/T]AGTACATTTTATTTA	55298
rs760805110	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71932409	GCCTGCCTGTGCTAT[A/G]TGGAGCTTAGCCCAT	55298
rs760917108	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71946107	CAGAGTAAGACTCTG[C/T]CTTAAAAAAGAAAAG	55298
rs761007970	snp	A/G	9.96578e-05	0.00705826	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960764	GGGTCGAGCACGCAC[A/G]CATGCATGCCAAGCA	55298
rs761113564	snp	A/C	1.64914e-05	0.00287149	intron-variant	RNF121	GRCh38.p7	11:71994886	CTGGGCCACATCTCT[A/C]CTGCAATCTGCACAC	55298
rs761184543	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71954715	TTCCAGATTTTCCTA[C/G]TTTCCCCCTCATTGG	55298
rs761242301	snp	C/T	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994749	GGCATGCCTACCAAA[C/T]ATCTTTCAGACAGTG	55298
rs761258666	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71952004	GAAAACATATATTCA[C/G]ACAAAAATTTAAAGA	55298
rs761378234	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71962684	GAAACTTAAACTCAT[A/G]TCTTTAGAAAATAAG	55298
rs761381369	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71963534	CTGAGGCAGGAGAAT[C/G]GCTTGAATCAGGGAG	55298
rs761414526	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71951940	GTTAAGCAGAGACTT[-/A]ACCATATGATCCAGC	55298
rs761431908	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71962591	TGCAGTTTACTTGTT[A/G]CTACCACATCCTGTA	55298
rs761457115	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71987309	AATGTCTGAATATAT[A/T]CAAAGTCAGAGTCCT	55298
rs761499465	snp	A/C	1.67089e-05	0.00289035	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996329	AGTGATGAAGAGCAT[A/C]AGTGGAAAACCCACC	55298
rs761501559	snp	C/T	1.66322e-05	0.00288371	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960885	GAGGCACCCACGCTC[C/T]TACAATGTAAGCCAC	55298
rs761557316	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71973352	AAAAATTAGCTGGTT[A/G]TAGTAGCATAGGCCT	55298
rs761577217	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71930792	ATATGTCAGGGTTCA[C/T]TGAGATAAACAGCAG	55298
rs761626174	snp	A/T	1.65993e-05	0.00288086	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996174	CTTGCACAGAGTCTC[A/T]TTTCTTTAACACACT	55298
rs761641468	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987045	TCTATAAAATCAGCT[A/G]TGCCACTGGCATTGT	55298
rs761691209	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71937678	TCTGTATTGCTTCAA[C/G]TTTTTAGTCCTTGTC	55298
rs761703685	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71970839	TTACCTTGCCTTAAG[A/C]CACACTATAAGAATA	55298
rs761715384	snp	C/T	1.67203e-05	0.00289134	intron-variant	RNF121	GRCh38.p7	11:71990554	AATCCATAGAAGATA[C/T]GTCTCAGGGTGGGTC	55298
rs761748054	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71955157	GTCCTGCAAGTGCAG[A/G]GTAGGTACCTGAGAG	55298
rs761801577	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71966180	GTGCGCCACCATGCC[C/T]AGCTAATTTTGTATT	55298
rs761826241	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71969285	GTTAGTTGTGATATA[G/T]TCACATAATGGAATA	55298
rs761850345	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71934719	AGTGGTGGCAAGTGT[A/C]GTGGGGAAAAAGCCA	55298
rs761886304	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980289	AAAGTGGTTCTGCTT[A/G]CCCTTTTCTCTGTTC	55298
rs762003529	snp	C/G	1.65748e-05	0.00287874	intron-variant	RNF121	GRCh38.p7	11:71957181	TTATATTGGCAGGGA[C/G]AGTTTTAAGACAGTA	55298
rs762020007	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944060	AGGTTGGCTGGGCAC[A/G]GTAACTCATGTCTGT	55298
rs762031644	snp	G/T	9.92572e-05	0.00704406	intron-variant	RNF121	GRCh38.p7	11:71957302	TGCAGTCTAGGAACT[G/T]CAGGTTAACCCAGCT	55298
rs762127412	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71992368	TTTAACTGTATGTGT[A/G]AAGCTACACATTTCA	55298
rs762129446	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71933586	AGGTGCTTGAAGCCA[C/T]CCTTTGAAAACCAAG	55298
rs762161580	snp	C/G/T			intron-variant	RNF121	GRCh38.p7	11:71949350	TTAGGCCTGGAAAGT[C/G/T]GACACTGCAGTGATC	55298
rs762190743	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979758	AAAGAGGATCTTAGC[A/G]CAGGCTGGTTGTTTT	55298
rs762385366	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939511	GCATGATTTTGTGGG[A/G]TGTTCTGGGTCAAGT	55298
rs762455275	snp	C/T	0.000265745	0.011524	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995500	TGGGAAAGAAGCAAA[C/T]GTGTCCCTACTGCAA	55298
rs762485320	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71971345	GCTGAGATCATGGCA[C/T]TTGACTACATTGTGG	55298
rs762486012	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71952103	TGAATGGATAAATAA[C/T]GTGGTATTTATACGA	55298
rs762510219	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71938006	ATGGCCATGGGGCTT[C/T]TGGCCCTGGGCAGCT	55298
rs762575268	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71992436	CTTAAGAGACAATTT[A/G]GTGTCTCTTAAATAG	55298
rs762581418	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953427	GTGTACAGATGCGTA[C/T]GGCTGTAGATGCAAT	55298
rs762602483	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963155	TCCTCACATTTTATC[A/G]GTTGTCTTGACACTT	55298
rs762617248	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71995572	CTTTATTGGGGTCGT[C/T]GTTGGGAGTGGGCTG	55298
rs762626824	snp	A/G/T			intron-variant	RNF121	GRCh38.p7	11:71950040	ACACACACAAAACTC[A/G/T]CACAAAAAACCCAAA	55298
rs762775090	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927821	CCGTATTAAGTGTCA[C/T]AAAATAAAAATGATT	55298
rs762779937	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71972340	TAGTAGAAACATGAA[C/T]TGTTTGAGATTAGCC	55298
rs762782614	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71948376	CAAAAATTAGCCGGG[C/T]GTGGTGGCTGCACTT	55298
rs762787173	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990858	TGCATATGCATGGAC[A/G]TTCCTTCCTTAAAGT	55298
rs762807606	snp	C/G	1.64749e-05	0.00287005	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987023	GTTTATAAGTGGTTC[C/G]TGCTAATCTATAAAA	55298
rs762899823	snp	G/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926973	ATACCTAAAAGGCTG[G/T]GTACAGTGGCTCACG	55298
rs762932889	snp	C/G	1.68946e-05	0.00290638	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982911	CTAGTACAGACAACC[C/G]CAAGGTGAGAGTTTA	55298
rs762975111	in-del	-/AAA			intron-variant	RNF121	GRCh38.p7	11:71986770	CGAGACTCTCATCTC[-/AAA]AAAAAAAAAAAAAAA	55298
rs763048651	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71951650	TCTTAAAAAAAAAAA[A/C]AAAAAACCATGGACA	55298
rs763087942	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71956531	CCAAATAGAACGAGA[A/G]CTTTGAAGTCGGATG	55298
rs763162954	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997092	GGCAGCCATGACTGA[C/T]GGCCCCTTGTGCAAG	55298
rs763197695	snp	G/T	0.000161668	0.00898933	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929042	GCGCGGGGACTGCGG[G/T]GAGGGGGCGAGCCGT	55298
rs763222159	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71932046	TCTGGAATGGCATTC[A/T]TTCATATTCCTTTTC	55298
rs763254619	snp	C/T	1.64925e-05	0.00287158	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960816	TGCTGAAATGGTCCT[C/T]ATCCTCATCGCAACC	55298
rs763321387	snp	A/C	1.65179e-05	0.00287379	intron-variant	RNF121	GRCh38.p7	11:71990725	CCATAGGGGTAAGTT[A/C]ATCCGGGTTCTTAAA	55298
rs763416386	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71976460	TCCCGGGTTCAAGCG[A/T]TTCTCCTGCCTCAGC	55298
rs763440714	snp	C/T	3.33039e-05	0.00408055	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996163	TCCTGGCAGCTCTTG[C/T]ACAGAGTCTCTTTTC	55298
rs763460790	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958762	CTGCTGGTTCTAAAA[C/T]AGATTACCTTAAAAG	55298
rs763523232	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983751	AGATGGACAAGAAAG[C/T]TCCTGTTGCAGTGCA	55298
rs763543711	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71949778	GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGTCCA	55298
rs763547433	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944258	GAATCACTTAAAGCT[A/G]GGAGGTGGAGGTTGC	55298
rs763625490	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71962437	TGAAGGTTGGGTAAC[C/G]CTAACACCTCTGCTT	55298
rs763674826	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961602	AATGGTTGAAATTAG[A/G]TGGGGAAAATGACAC	55298
rs763698859	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71961265	TTACACTAATCTAAA[-/T]TTTTTTAAAGAAGGA	55298
rs763739710	in-del	-/TCT			intron-variant	RNF121	GRCh38.p7	11:71943059	AAGGTTCCCTCCACC[-/TCT]TCTTAATACTATTGC	55298
rs763801254	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71973953	GTTTGTTTGTTTGTT[C/T]GTTTTTGAGACGGAG	55298
rs763804141	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71992581	GTTTCCAAGAAACTG[C/T]CAGTGAAGTGAGGAC	55298
rs763851138	snp	A/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928167	GTGTGTGAACTGGCA[A/T]GACAGCCTAAGTAAG	55298
rs763868892	snp	A/G	1.69746e-05	0.00291325	intron-variant	RNF121	GRCh38.p7	11:71982918	AGACAACCCCAAGGT[A/G]AGAGTTTAAGTAGTG	55298
rs763875195	in-del	-/AAA			intron-variant	RNF121	GRCh38.p7	11:71988641	AGACTCTCAACTCTT[-/AAA]AAAAAAAAAAAAGAA	55298
rs763897433	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71968093	TTAAGATGAAGTCCT[G/T]CTCTGTCGCCCAGTT	55298
rs764042875	snp	A/C	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987031	GTGGTTCCTGCTAAT[A/C]TATAAAATCAGCTAT	55298
rs764070374	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71981638	GAGTTAGAATTGTTT[C/T]ATGCCTTTAAAAAAC	55298
rs764086034	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71936843	TTTAATGCAGGGACT[A/G]TTTTTCTCATCTTTG	55298
rs764127526	snp	A/C/G			intron-variant	RNF121	GRCh38.p7	11:71980639	GGTGTGAGTCACCAC[A/C/G]CCTGGCCATCTAAGG	55298
rs764128553	snp	A/G/T	6.61675e-05	0.00575152	intron-variant	RNF121	GRCh38.p7	11:71990591	GCTCTAATGCTTCCC[A/G/T]TGCAGGATCAAACCA	55298
rs764199472	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965063	TGACATAGAAATCAA[A/G]AGTGTCCCAGAGGGA	55298
rs764226176	snp	C/G	1.65225e-05	0.00287419	intron-variant	RNF121	GRCh38.p7	11:71990728	TAGGGGTAAGTTCAT[C/G]CGGGTTCTTAAATAC	55298
rs764326149	snp	C/T	0.000534188	0.0163343	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978100	GAGGTGGGGTTTCAC[C/T]GTGTTGCCCAGGCTG	55298
rs764349418	snp	A/G	1.66029e-05	0.00288117	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960881	AGCAGAGGCACCCAC[A/G]CTCCTACAATGTAAG	55298
rs764375467	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71948344	AACGTGGTGAAACCC[C/T]ATCTTTACTAAACGT	55298
rs764415358	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71972720	CTGCCAAATGTCCCC[C/T]GGGAAACAAAATCAT	55298
rs764473509	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71986280	CCTGTAGCTCATTCT[A/T]CCTCTGATTCATCTC	55298
rs764557251	snp	A/T	1.64923e-05	0.00287156	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960817	GCTGAAATGGTCCTC[A/T]TCCTCATCGCAACCT	55298
rs764567757	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71966144	CCTGCCTCAGCATCC[C/T]GAGTAGCTGGGATTA	55298
rs764570012	snp	A/C			upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997703	TGGGGGTGGTTGGGC[A/C]TGCCTTTCTGCTGTT	55298
rs764619181	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71956791	TATTTCTCTTATTTC[C/T]TCTTCTGGATAATTC	55298
rs764626157	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940017	ATTAAAGAAGACTTC[C/T]GATAGGGTATGGCAT	55298
rs764629235	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981872	GGAGCTTACATACAG[A/G]TAGAGAATGAATTCA	55298
rs764673808	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71959825	ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT	55298
rs764675182	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71950687	AGGCGGAGTCTTGCT[C/G]TGTCTCCCAGGCTGG	55298
rs764685110	snp	G/T			missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960891	CCCACGCTCCTACAA[G/T]GTAAGCCACTTTGCC	55298
rs764751112	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71953942	TTTCCCTCTGCCTAG[C/G]ATTTATTTTTGGTTT	55298
rs764767610	snp	A/G	8.81329e-05	0.00663767	missense, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71995501	GGGAAAGAAGCAAAC[A/G]TGTCCCTACTGCAAA	55298
rs764801247	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951498	TAGTCTCAGCTACTT[A/G]GGAGGTAGTCCCAGC	55298
rs764828103	in-del	-/AAC			intron-variant	RNF121	GRCh38.p7	11:71955576	TGTAGATAAGAAACA[-/AAC]AACAACAACAACAAC	55298
rs764923634	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71935173	CCTGGACTCAAGCAA[C/T]CCACCTGCCTTGGCC	55298
rs764962423	in-del	-/AG			intron-variant	RNF121	GRCh38.p7	11:71948100	CAGTGCATATAGGAA[-/AG]AGTGAGAGAGGAGGG	55298
rs765039735	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944194	AAAAATTAGCCAGGC[A/G]TGGTGGCATGCACCT	55298
rs765153603	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958757	AGACACTGCTGGTTC[C/T]AAAATAGATTACCTT	55298
rs765161054	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71957469	TGCACCAAATCATCT[A/G]TCTGGGTTTCAATAC	55298
rs765203012	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937905	TGAAGTCATTTGCTA[C/T]CTCTACTCCTCAGAG	55298
rs765242853	snp	A/G	1.75059e-05	0.00295849	intron-variant	RNF121	GRCh38.p7	11:71982728	CTGCAGAGGGAGCTG[A/G]CCAGAGCTGAAGTGC	55298
rs765331481	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71969419	AGTGCAAAAGAAGAG[A/T]CCTAGAAGACCACTT	55298
rs765331989	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71968034	ATTTGTAGAATTGGT[A/G]GAAAAATTTTTATAG	55298
rs765341855	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987079	CTACATGGCTGTCAT[A/G]TTTACCCTCTTTGGT	55298
rs765348675	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71970445	GTGGAAGGATCACTT[G/T]ATTCCAGGAGTTCCA	55298
rs765356338	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71986770	CGAGACTCTCATCTC[-/AA]AAAAAAAAAAAAAAA	55298
rs765363558	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996097	TCTAGGCTGTGGAGC[A/G]GCTGGAAAGTGGGGC	55298
rs765390079	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927515	AACACAGCGAGACAC[C/T]GTTTCAAAGAAAAAA	55298
rs765415794	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71941845	AAATGGTTCTGTATG[A/G]GGTCAGGGAGTCTGG	55298
rs765419497	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71933627	TTATAGTCCACTGAT[C/T]GGGTGACCCCACTTC	55298
rs765435402	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997005	GAATCAGCACCATGG[A/T]TACTCGCCCGTGGGC	55298
rs765486015	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71934722	GGTGGCAAGTGTAGT[A/G]GGGAAAAAGCCATAG	55298
rs765486630	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71961756	TCATTTATCGATATG[C/G]TGTCTATAGTAAATT	55298
rs765510381	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71979264	TCCTCCAAGAAAGGA[C/T]GGAGGACCTCCTTAG	55298
rs765511327	snp	A/G	4.56423e-05	0.00477693	missense, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71995495	CATCGTGGGAAAGAA[A/G]CAAACGTGTCCCTAC	55298
rs765577173	snp	A/C	1.65531e-05	0.00287686	intron-variant	RNF121	GRCh38.p7	11:71990588	CTAGCTCTAATGCTT[A/C]CCTTGCAGGATCAAA	55298
rs765600229	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980081	GAAAATGACACCTGG[A/G]GCATTATTTGGGTAG	55298
rs765611739	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71974164	GCCAAGATGGTCTCA[A/G]TCTCCTGACCTCGTG	55298
rs765681050	snp	C/T	0.000165049	0.00908281	intron-variant	RNF121	GRCh38.p7	11:71994899	CTCCTGCAATCTGCA[C/T]ACTGTAGTGAGAGAG	55298
rs765706995	snp	G/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929740	CTTAATAAACATTAT[G/T]ACTTTTGCTCCGGGT	55298
rs765745536	snp	G/T	9.89544e-05	0.00703331	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960812	TGCATGCTGAAATGG[G/T]CCTCATCCTCATCGC	55298
rs765775487	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71971366	TACATTGTGGGTAAC[A/G]GATGAAACCCTGTCT	55298
rs765804126	snp	A/G	1.75526e-05	0.00296243	intron-variant	RNF121	GRCh38.p7	11:71982710	TTGGGACTGTGGACA[A/G]AGCTGCAGAGGGAGC	55298
rs765825980	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71941338	TTTTGCCCTTTATTT[A/C]TCTCCCTAATTCGTT	55298
rs765835119	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926987	GGGTACAGTGGCTCA[C/T]GCCTGTAATCTCAAC	55298
rs765859058	snp	C/T	1.6817e-05	0.0028997	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996343	TCAGTGGAAAACCCA[C/T]CCCACACGCCATGGA	55298
rs765912998	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71986533	AACACTTTGGGAGGC[C/T]GAGGCGAGTGGATCA	55298
rs765924350	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983069	AAGCTGATTGGTAGA[A/G]CCCCTCCCCTATTTA	55298
rs765963422	snp	C/T	1.68204e-05	0.00289999	intron-variant	RNF121	GRCh38.p7	11:71960915	CTTTGCCTCTTACTT[C/T]TTTGTCTGTCAGTCA	55298
rs766017709	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938130	TCAATGTATTCTGTT[A/G]CTTAGAAGCCTCAAC	55298
rs766059980	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71981941	TTAGAAAAGAAAATG[A/C]GTTTGGAGCACTAGA	55298
rs766070891	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71930542	ACCTCCCAATCACTA[-/G]GAGACTACAGGTGTT	55298
rs766181253	snp	C/T	0.000121322	0.00778759	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929039	CTCGCGCGGGGACTG[C/T]GGTGAGGGGGCGAGC	55298
rs766271130	in-del	-/TTTG			intron-variant	RNF121	GRCh38.p7	11:71934507	AGTAATCACTGGTTT[-/TTTG]TTTGTTTGTTTGTTC	55298
rs766303308	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71948387	CGGGCGTGGTGGCTG[A/C]ACTTGTAGCCCCACC	55298
rs766309796	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71990915	AGATAAAACCATGTG[C/T]GTTGCAGCAACATGC	55298
rs766330352	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71941933	CGTGTAATGAGAATT[-/T]TTTTTTTTTTTTTTT	55298
rs766352565	snp	A/G/T			intron-variant	RNF121	GRCh38.p7	11:71960391	TTGGGTTACTTTCTC[A/G/T]TTCCAGCATCAGGTT	55298
rs766354483	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71946538	TCAGCTGCTGAATGA[A/G]TTCATTTGTATGAAA	55298
rs766375215	snp	A/C	1.64898e-05	0.00287135	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996213	GGAGAGGCCTCACGT[A/C]ATGTATGGGCAACTG	55298
rs766399712	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71972377	GCTTTTAAAAAAATG[C/T]CTCTTATGGCATTCC	55298
rs766484045	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71959064	TATGGACTCCTTTTG[A/T]CAGATGAAGAAATTG	55298
rs766496157	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71970953	TAAGAAGGTATTCAT[C/T]GTTAAGTAGATTAGT	55298
rs766532322	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71981850	ATGGCCCAGTCACTA[-/C]CCACAAGGAGCTTAC	55298
rs766581247	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71974052	GTTCACGCCATTCTC[A/C]TGCCTCAGCCTCCTG	55298
rs766664470	snp	A/G	4.94173e-05	0.00497053	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994750	GCATGCCTACCAAAC[A/G]TCTTTCAGACAGTGT	55298
rs766672930	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71995656	CACTTCTGCCCCCAA[A/C]CAGAACATGTCAAAC	55298
rs766678152	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71986610	GTCTCTACTAAAAAA[A/T]ATATAAAAATTAGCC	55298
rs766738124	in-del	-/G	1.70621e-05	0.00292074	intron-variant	RNF121	GRCh38.p7	11:71982928	AAGGTGAGAGTTTAA[-/G]TAGTGGGAAGAGCCC	55298
rs766781794	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71931101	GTCCTCCCAAATGTG[C/T]TGGGATTACAGGTGT	55298
rs766802326	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963720	CTAAGTTCATTCTTT[C/T]GCATGTGGATAGCCA	55298
rs766813805	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71949373	CAGTGATCTGTGATT[-/G]CACTACGGCACTCCA	55298
rs766895501	snp	A/G	1.64947e-05	0.00287177	intron-variant	RNF121	GRCh38.p7	11:71994891	CCACATCTCTCCTGC[A/G]ATCTGCACACTGTAG	55298
rs766895638	snp	A/G/T	6.59015e-05	0.00573995	intron-variant, missense, utr-variant-5-prime	RNF121	GRCh38.p7	11:71957231	TCTTTCTACAGGTTG[A/G/T]TATGTCAGATCTCTC	55298
rs766912083	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71944293	AGCCGAGATTGTGCC[A/G]CTGCACTCCTGCCTG	55298
rs766950412	snp	C/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928027	CTTGCAAGGTATCGA[C/G]TTCACCGGCTGCTGA	55298
rs766996154	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71989485	ATCTTGATCATTTTT[A/G]TGCTACTGATCAAAT	55298
rs767048878	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71973643	AATACAAAAATTAGC[C/T]GGATGTGGTGGCAGG	55298
rs767061685	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975621	AGTAGACTTGTGTTC[C/T]TCAGGAGATTTTGGT	55298
rs767069777	snp	C/T	1.65946e-05	0.00288046	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996175	TTGCACAGAGTCTCT[C/T]TTCTTTAACACACTG	55298
rs767070708	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71940812	AGGGAGTGATTAACT[C/G]TGCTTCGGGAATCCT	55298
rs767071829	snp	A/G	1.64914e-05	0.00287149	missense, nc-transcript-variant, utr-variant-5-prime, synonymous-codon	RNF121	GRCh38.p7	11:71960823	ATGGTCCTCATCCTC[A/G]TCGCAACCTTGGTGG	55298
rs767128617	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71953991	GCATGACTGGGGGCC[G/T]TGTGAGATCCTAGTT	55298
rs767187597	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71980431	AGCTTGCCGCAACCT[C/T]CACCTCCCGGATTCA	55298
rs767195135	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927234	CCTGGGCGACAGAGC[C/T]GGACCCTGTATCACT	55298
rs767269061	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987054	TCAGCTATGCCACTG[A/G]CATTGTTGGCTACAT	55298
rs767340385	snp	G/T	1.67063e-05	0.00289014	intron-variant	RNF121	GRCh38.p7	11:71990561	AGAAGATATGTCTCA[G/T]GGTGGGTCTTTCTAG	55298
rs767380725	in-del	-/AC			intron-variant	RNF121	GRCh38.p7	11:71950016	AAAACAAAACAGAAC[-/AC]ACACACACACACACA	55298
rs767405956	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71948623	GCTGTAGCAGCTGTT[A/G]GAGCCAACATCTACT	55298
rs767420101	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949490	GAGGCCCAGGCAGGC[A/G]GATCACTTGAGGTCA	55298
rs767442030	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71935274	CATAACCTTATAAGA[G/T]ATGTACTATTATTAT	55298
rs767442359	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979464	CTTTTTCTTTCTCTC[A/G]ATGTGACTTGATATA	55298
rs767538042	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937971	TCTAAAGTGCAGCTT[C/T]CCCAAGAGGATGCTG	55298
rs767607088	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931131	TGAGTCACCGCGCCC[A/G]GCTAAGAAAATAACA	55298
rs767634045	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71950471	CACCTGTAATCCCAG[A/C]TACTGGGGAGGCTGA	55298
rs767634575	snp	G/T	4.96381e-05	0.00498162	intron-variant	RNF121	GRCh38.p7	11:71957184	TATTGGCAGGGACAG[G/T]TTTAAGACAGTAACG	55298
rs767687776	snp	A/C	1.64732e-05	0.0028699	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994745	GTCGGGCATGCCTAC[A/C]AAACATCTTTCAGAC	55298
rs767752991	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71989662	AAGATTTATAGACTC[A/G]AGGTTGCAAATTATC	55298
rs767809147	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71934739	GGAAAAAGCCATAGG[A/G]TAGTAAACAGTGGGT	55298
rs767817654	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983142	GTTTCAAGGTATTTT[C/T]ATATTAAAGGCAAAC	55298
rs767858945	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938683	ATTCTCCTACCATAA[A/G]CTTTTGTTTCATCCA	55298
rs767933325	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997358	CATGGGTCCTCCCTG[A/G]GCCTGACAACGGGAG	55298
rs767943902	snp	C/G	1.65367e-05	0.00287543	intron-variant	RNF121	GRCh38.p7	11:71990735	AAGTTCATCCGGGTT[C/G]TTAAATACTGCTTCT	55298
rs768024639	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71953639	TAGCAAGGCAGTAGA[A/G]GATGTTTGTTCTTCA	55298
rs768054953	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71932112	GAAGTTGAGACGTAA[C/T]TTAGGCTTTCCTAAT	55298
rs768071862	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71952279	AGGCAAATCTATAGA[C/T]AGAGACAGAATGTAA	55298
rs768170847	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990060	TTGTGCTCTGTTGTC[A/G]TAAGCTGAGACAATC	55298
rs768198727	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71964030	TAATTTTAATATCAA[C/T]GTTTCCATTTTACAA	55298
rs768199747	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71987726	AAAAGTTTGCTGACT[C/T]TTGGGCTAGACCGTC	55298
rs768229344	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71931533	TAGCTTGTGAAACAG[C/G]AGGTGAAATCCGTCT	55298
rs768236338	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71956949	CTGTCTTTCTCACTA[C/G]TCTGTGAGCGTCTTT	55298
rs768238812	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71975282	TCTTCAGAATATAAC[A/G]AAAACTTGTAGCTGT	55298
rs768242154	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71976192	TTTTATTATAATCCT[A/T]GCTGCTCTCTTATGG	55298
rs768342382	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71989115	TTTGAGATGGAGTCT[G/T]GCTTTGTCGCCTAGG	55298
rs768413390	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71943862	AGAGAATGCCACCTT[C/T]AGGGAACTGTATGCA	55298
rs768434800	in-del	-/TTAA			intron-variant	RNF121	GRCh38.p7	11:71955184	AGAGTGAGTGCTTCC[-/TTAA]ATTTTGAGCCCCAGG	55298
rs768471351	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951896	AATGGTACAGCTGCC[A/G]TGGAAAACAGTTTGC	55298
rs768533109	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997230	TGTGTGTGTGTGTAC[A/G]TGAGGCAGAAGAATA	55298
rs768533495	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71982558	GAATATATCCAAGAG[A/T]TAGTTGAGTGAGGGA	55298
rs768627892	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963505	CGTGCCTGTAATCCC[A/G]GCTACTCGGAAGGCT	55298
rs768634763	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71949192	GCAGGCTGGGGTGAG[C/T]GGGTCACTTGAGCCC	55298
rs768683021	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71992971	CCCCACCCCAAGAAG[C/G]AATATTTCCATCACC	55298
rs768683639	in-del	-/TA			intron-variant	RNF121	GRCh38.p7	11:71951617	CTCCAGCCTGGGCAC[-/TA]TATAGCAAGACCCTG	55298
rs768689391	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71979143	TTGAATGAGTGAGTG[C/G]GTGAACACTGCCTCT	55298
rs768696787	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996189	TTTTCTTTAACACAC[C/T]GACAGCTGGGAGAGG	55298
rs768716454	in-del	-/TATT			intron-variant	RNF121	GRCh38.p7	11:71984592	CCAGTAACTACTAGC[-/TATT]TATTTATTTATTTAT	55298
rs768729019	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929198	AGGTATCGGGAGGTG[A/G]GGGTCTTAGGAGAGA	55298
rs768744942	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71950514	GCTTGAACCCAGGAG[G/T]TGGAGGTTGCAGTGA	55298
rs768778164	in-del	-/TGAGATGGAGTCTTGCTTTGTCGCC			intron-variant	RNF121	GRCh38.p7	11:71989102	TTTGTTTGTTTGTTT[-/TGAGATGGAGTCTTGCTTTGTCGCC]TAGGCTAGAGTGCAG	55298
rs768790969	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71956256	CTGTAGATCAGATCA[A/C]AGAACATTTTCAGCT	55298
rs768824219	in-del	-/TTT			intron-variant	RNF121	GRCh38.p7	11:71941931	AGCGTGTAATGAGAA[-/TTT]TTTTTTTTTTTTTTT	55298
rs768910519	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71957914	CAACCTTAGAATTTA[A/G]TAGTGAGAAAAAACC	55298
rs768911991	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71933722	CTCACTAGACTGTAA[-/G]CTTCGTGAGAGAGCA	55298
rs768989195	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927427	TTGGGAGGCTGAGAC[A/G]TGAGAATCGTTTGAA	55298
rs769006751	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939704	GAACATGGTGATACA[A/G]CCTCATGTCTTCATG	55298
rs769127934	in-del	-/TTTTT			intron-variant	RNF121	GRCh38.p7	11:71984746	GCCACACCCGGCTAA[-/TTTTT]TTTTTTTTTTTTTTT	55298
rs769139149	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71967796	CCCAATTTTTAAATA[A/T]ATATTCATTGTTTAC	55298
rs769177336	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71966898	GAGACGGAATCTCAC[A/T]CTGTCACCCAGGCCG	55298
rs769181176	snp	A/G	6.65535e-05	0.00576822	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996164	CCTGGCAGCTCTTGC[A/G]CAGAGTCTCTTTTCT	55298
rs769208453	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980218	TTATTGAGGCTTCAA[A/G]GCTCATGGACCAGCA	55298
rs769264693	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963543	GAGAATCGCTTGAAT[C/T]AGGGAGTTGGAGGTT	55298
rs769277637	snp	C/T	1.64827e-05	0.00287073	intron-variant	RNF121	GRCh38.p7	11:71986993	GCACTAACCTTCTCT[C/T]CTTTCCCCAGGTTGG	55298
rs769411619	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71975901	AAGAGCTGTCTAGCA[A/G]ATATATTCGTATTGG	55298
rs769423332	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71977098	TCTATTTCTCAGCCT[A/G]TTTTCAAGCTGATTG	55298
rs769435418	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71986771	GAGACTCTCATCTCA[-/AA]AAAAAAAAAAAAAAA	55298
rs769477206	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926771	CTGGGTGTGGTGGCA[C/T]ATGCCTGTAATCCCA	55298
rs769496030	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933028	TCTCAGCCTGCCAAA[A/G]TACAGCATGCTTGAG	55298
rs769546656	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71994969	CCCTTGAGTGTAGGA[A/G]AGCCACAAGAGGGCC	55298
rs769546847	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931571	GTAATTATGGGGTCT[A/G]CTGTGTGTTATGCAC	55298
rs769580862	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927687	TAATAGGCTTGAGAG[C/T]AGAAAAAACAGGTAA	55298
rs769582313	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990397	GTCTTCACAGCCTAC[A/G]GTGCTAGCTAGCCTC	55298
rs769583280	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940472	AGCATTAGGAATGAA[C/T]GCCCAAGGTCAATGT	55298
rs769606217	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71983926	CCTTTCTCTGGCCTT[C/T]TGGAGTTTCATTGTA	55298
rs769624708	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997440	GCCCTAGTCCTAGGC[A/G]ACTTGAATAAAGTGG	55298
rs769670625	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71985499	GTGATCAGTGCAATC[C/T]CTGGAGAATAGAGCT	55298
rs769672896	snp	C/G	1.64743e-05	0.00287	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994840	ACACGTATAGGCTGT[C/G]CTGCAATCATGTGTA	55298
rs769709974	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71939434	CAACTTCCCTCCACC[C/T]CTATGGCCTGGGCAG	55298
rs769737667	snp	A/T	0.000741015	0.0192343	intron-variant	RNF121	GRCh38.p7	11:71978082	TGTATTTTTTTTTTT[A/T]AAGAGGTGGGGTTTC	55298
rs769741026	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972164	AATTAATAAAAATAC[A/G]AGCAGAGAAAGCAAT	55298
rs769766812	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71953388	TGAGTTAGATCTCTG[C/T]AAAGTTGTTAAATAA	55298
rs769893003	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71995020	CAGATCAGAGCCACT[C/G]TTAGGTAAACAGTGG	55298
rs769946355	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71980297	TCTGCTTACCCTTTT[C/G]TCTGTTCTGTTCTGT	55298
rs769953600	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71937344	TATTTTTTTGAGACA[A/G]AATCTTGCTCTGTTT	55298
rs770016233	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71945026	GACAGGGTCTTCTGT[C/T]ACCCAGGCTGGAGTG	55298
rs770060058	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71993015	ATCTAGTACCGTTTA[A/C]GGCCAGGGACTTTGT	55298
rs770068058	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71958102	GATGTTCGTAGAAAT[A/G]TGCTGTCTGCTGTAA	55298
rs770121817	in-del	-/T/TT/TTT			intron-variant	RNF121	GRCh38.p7	11:71967349	TGTGGGTTTTTTTTG[-/T/TT/TTT]TTTTTTTTTTTTTTT	55298
rs770159635	snp	A/G	1.65051e-05	0.00287267	utr-variant-3-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996279	TGTCATCATTGGTGT[A/G]GTCCAAGGCATCAAC	55298
rs770183445	snp	C/G			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962221	GATCCGCCTCGGCCT[C/G]CCAAAGTGCTGGGAT	55298
rs770242860	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71989301	GGCGAGGCTGGTTTC[A/G]AACTCCTGACCTCAG	55298
rs770251979	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71985372	CACCTCTCTTGTCTC[-/AA]AGAGGTGATTTGACT	55298
rs770335200	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71968747	CAGTTATATTGTTTC[A/C]TTTGTGGAGAAACAA	55298
rs770346530	snp	A/T	1.66504e-05	0.0028853	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996158	ATCACTCCTGGCAGC[A/T]CTTGCACAGAGTCTC	55298
rs770355451	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71982425	TGGTGAAGATTTCGT[C/G]TTCGAGATACCATTC	55298
rs770433991	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71984502	TAGCCAGGATGTCTC[A/G]ATCTCCTGACCTCAT	55298
rs770436184	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71940681	CTGGGGACACAAAGA[A/T]GAAAATGTGGCTCCT	55298
rs770450092	snp	C/G	4.95888e-05	0.00497915	intron-variant	RNF121	GRCh38.p7	11:71986965	CATTAAGGCCAGAAT[C/G]TCTGTGTCAGCTGCA	55298
rs770547802	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997480	CATGGGCCTTCGGCA[C/T]TGGGTTTCTAGGGAA	55298
rs770619304	in-del	-/AT			intron-variant	RNF121	GRCh38.p7	11:71959304	AAAAACTTTAAACAC[-/AT]AGAAAAGTTGAAAGA	55298
rs770628367	snp	A/G	6.65347e-05	0.0057674	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982888	CCTTCCGAGCCACCC[A/G]AAAACCTCTAGTACA	55298
rs770760726	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71942135	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	55298
rs770876177	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71961285	TTAAAGAAGGATCGG[G/T]TGTGGTGGCTCATGT	55298
rs770904090	in-del	-/AG	0.000149747	0.00865164	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996166	TGGCAGCTCTTGCAC[-/AG]AGTCTCTTTTCTTTA	55298
rs771042122	snp	G/T	0.0306376	0.119917	synonymous-codon, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71995478	TGCATCCGTGGCTGG[G/T]GCATCGTGGGAAAGA	55298
rs771120857	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71969045	TGTCTGCCACCATGC[C/T]CGGCTAATTTTTGTA	55298
rs771137658	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938679	ATTTATTCTCCTACC[A/G]TAAGCTTTTGTTTCA	55298
rs771223370	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71951835	ATAAGTACTGGGAAG[G/T]ATATGGAGAAATTGG	55298
rs771298012	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947926	AAAACTCAAGGGAGA[C/T]TTTATAGATGTTTAG	55298
rs771303913	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985519	AGAATAGAGCTGTGT[A/G]TGTTCTTTAAGACAA	55298
rs771341530	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71932085	TGTCTGGTTTCATTA[A/G]TACTTTCTCTAGAAG	55298
rs771353338	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71965254	ATGACTGCATAGTAA[-/T]TTTTTTTTTTTTTTT	55298
rs771441227	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71943610	AAGACATAGGCCTTG[C/T]TCTCAGGTTGCTCAT	55298
rs771456706	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71977328	CAGGGAAAGATATGA[A/T]CTATTTTCATGAATT	55298
rs771588907	snp	A/G	9.75087e-05	0.00698175	utr-variant-5-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929109	TGGTGCTGCTGGGGA[A/G]CGGGAGCTGGATGAG	55298
rs771619011	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71945810	TAATAAAAAAAATAA[C/T]CTAGTAAAAAATGGG	55298
rs771621898	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71942217	GGATTACAGGCATGA[A/G]CCACCGTGCCCGGCA	55298
rs771713037	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927362	ACCCCATCTCTGCTA[A/G]AAATATGAAATTTCC	55298
rs771783214	snp	A/C	3.34135e-05	0.00408725	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996330	GTGATGAAGAGCATC[A/C]GTGGAAAACCCACCC	55298
rs771834110	snp	A/G			intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962256	GGCGTGAGCCACCGC[A/G]CCCGGCAGATTTTTA	55298
rs771841262	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71955975	TAAATTTATTTTTTG[A/G]CTTAGCTGGGAGATG	55298
rs771898394	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954487	CAACATTCAATTATC[C/T]CTGGCCTCTTCTAGT	55298
rs771917842	snp	A/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990653	TCTTCTATGGCCTCT[A/G]CTATGGAGTTCTGGA	55298
rs771927462	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975986	ACAACTCCAACCGTG[C/T]TTCTGCCTTGTAGAG	55298
rs771949247	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71995153	TGGGATCCCTCAGTT[C/T]AGCATCATCCTCTGT	55298
rs771978247	snp	C/G			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996690	ACTGCTGGGCTCCCA[C/G]GTAGCTGAAGGCCTC	55298
rs771999630	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990522	TTTGGGCCCTGCCTT[A/G]TGTGTCCCAGAGTAG	55298
rs772003983	snp	A/G/T	6.61074e-05	0.00574891	intron-variant	RNF121	GRCh38.p7	11:71994681	TTGGCTGCTTCTCAC[A/G/T]TCTTTTCCTATCTTT	55298
rs772031081	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71955891	AATAAATTCTGTGAG[C/G]CAGTGTGGGTAGGAA	55298
rs772044450	snp	A/C	4.94727e-05	0.00497332	intron-variant	RNF121	GRCh38.p7	11:71994882	GCTCCTGGGCCACAT[A/C]TCTCCTGCAATCTGC	55298
rs772051833	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71974726	GACTTTTGCCCAAGT[C/G]CTTTCCTTGGATCTC	55298
rs772066606	snp	G/T	3.49999e-05	0.00418315	intron-variant	RNF121	GRCh38.p7	11:71995584	CGTTGTTGGGAGTGG[G/T]CTGTGGGAAGAAAGT	55298
rs772066814	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71959838	ACGGGGTTTCGCCAT[A/G]TTGGCCAGGCTCATC	55298
rs772107557	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927508	CCTTGGTAACACAGC[A/G]AGACACCGTTTCAAA	55298
rs772117830	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972095	TGGGAGGACCTTAAA[A/G]GCATAGTACTGAGTG	55298
rs772123476	in-del	-/TTG			intron-variant	RNF121	GRCh38.p7	11:71931372	CTGGTTCTATCTTTT[-/TTG]TTGTTGTATGTTTGA	55298
rs772182822	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71939506	GATTTGCATGATTTT[G/T]TGGGGTGTTCTGGGT	55298
rs772199873	snp	A/C/T	3.37452e-05	0.00410751	intron-variant	RNF121	GRCh38.p7	11:71957303	GCAGTCTAGGAACTG[A/C/T]AGGTTAACCCAGCTT	55298
rs772210918	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979148	TGAGTGAGTGGGTGA[A/G]CACTGCCTCTACTCT	55298
rs772299278	snp	A/G	7.63621e-05	0.00617861	splice-acceptor-variant, intron-variant	RNF121	GRCh38.p7	11:71995439	CATTTCCCTTGACCA[A/G]CGGTGCTCAGCTTCC	55298
rs772352811	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980127	TCCTGGTGCTTCCAC[A/G]CTTTTTATGTAAGGT	55298
rs772392566	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71970618	AGTAAACTATGATCA[A/C]GTCACTGCACTCCAG	55298
rs772407873	in-del	-/CT			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928226	CGCAAGGCTCTTCAG[-/CT]CTCAGTTTCGGGAGC	55298
rs772427460	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71934281	ATGGATAAAGTGTGA[A/T]AATTGTCCTCAGAAA	55298
rs772475549	in-del	-/TAAA			intron-variant	RNF121	GRCh38.p7	11:71967790	CCTCCTCCCAATTTT[-/TAAA]TAAATATTCATTGTT	55298
rs772552733	snp	A/G	1.64955e-05	0.00287184	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982863	TTCTCTGCTGTCACA[A/G]CCTTTGTTACCTTCC	55298
rs772560241	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71937085	TTCATTGGATTCATT[A/T]AAATTAATGCCAAAT	55298
rs772569770	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71978828	GTTTAGAGAACTGAA[A/G]CTTTTCAGAGTTAAA	55298
rs772593248	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71982972	CTAATGGGTTGGAAT[C/G]CATGGGAGGAGCATA	55298
rs772603092	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71948085	GTATATGGAAAGCTG[C/G]AGTGCATATAGGAAA	55298
rs772605045	in-del	-/TG			intron-variant	RNF121	GRCh38.p7	11:71938826	TTTGGTTTTGAGCTC[-/TG]TAAATATGGCAGTGC	55298
rs772613481	snp	A/C			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996579	GGAGCATAGGAATTG[A/C]CCCCCTCCAGGCTTC	55298
rs772641449	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71991876	TTGGGAGGCTGAGGC[A/C]GGCAGATTGCTTGAG	55298
rs772673787	snp	C/G/T	0.000115459	0.00759724	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960852	GGTGGCCCAGCTGCT[C/G/T]CTGGTGCAGTGGAAG	55298
rs772701448	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71964713	CGCCCTCCTGAACTC[A/G]AGCAATCCGCCTGCC	55298
rs772770281	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71986772	AGACTCTCATCTCAA[-/A]AAAAAAAAAAAAAAA	55298
rs772772293	snp	C/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997467	GTGGGAGGTCAAACA[C/T]GGGCCTTCGGCATTG	55298
rs772862648	in-del	-/AC			intron-variant	RNF121	GRCh38.p7	11:71952152	ACAAACGAATGAACT[-/AC]ACAGTACATGCTACA	55298
rs772932348	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71963574	GCAATGAGCCAAGAT[C/T]GCACCACTGCACCCC	55298
rs772954188	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71966908	CTCACTCTGTCACCC[A/T]GGCCGGACTGCGGAC	55298
rs772975251	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71931971	AAGTTACACGCTGTG[C/T]ATATTCAGGATATTA	55298
rs772997193	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71948513	AGTGAAACTGTCTCC[-/A]AAAAAAAAAAAAAAA	55298
rs773010298	in-del	-/TGTT			intron-variant	RNF121	GRCh38.p7	11:71934174	TTTTATGGTTTTCTC[-/TGTT]TAAGTTTGTTCCCTC	55298
rs773012443	snp	C/T	3.29489e-05	0.00405874	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990670	TATGGAGTTCTGGAA[C/T]GGGACTTTGCAGAAA	55298
rs773015044	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977142	GGATCTCTACCTTTA[C/T]TCTACTACTTGGGCT	55298
rs773039916	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71965607	TTTATCGATTGACTT[G/T]TTAATTAACAGTTTA	55298
rs773186287	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71950016	AAAAACAAAACAGAA[C/T]ACACACACACACACA	55298
rs773202694	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71939480	AGTGAATATGAAGAT[G/T]TTAATATCTTGATTT	55298
rs773203916	in-del	-/CTTA			intron-variant	RNF121	GRCh38.p7	11:71981766	TAGTTTTACTTTCCT[-/CTTA]CTTATCGGAATTTAT	55298
rs773252928	snp	C/G/T			intron-variant	RNF121	GRCh38.p7	11:71973615	AACATGGTAAAACCC[C/G/T]GTCTCTACTAATAAT	55298
rs773284647	snp	C/G	8.24504e-05	0.00642016	intron-variant	RNF121	GRCh38.p7	11:71994884	TCCTGGGCCACATCT[C/G]TCCTGCAATCTGCAC	55298
rs773317536	snp	C/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997044	GGTCAGCCAAGAATA[C/G]AGGTCATATAGTTGG	55298
rs773416873	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71931054	GGTCAGGCTGGCCTC[A/G]AACTCCTGACCTCAG	55298
rs773510541	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71936160	ACTGCTGCGCCTGGC[C/T]TATAATTATTCTTAA	55298
rs773545556	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71944256	GAGAATCACTTAAAG[C/T]TAGGAGGTGGAGGTT	55298
rs773622030	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976420	GAGTGCAGTGGCACA[A/G]TCTCGGCTCACGGCA	55298
rs773635802	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71956772	AGTCCCTTTGCCTGG[A/G]ATGTATTTCTCTTAT	55298
rs773661340	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958151	TGTGGTCTGCTCTGC[C/T]GAGGTCACAAATATT	55298
rs773723841	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71958732	TATGTATATGTACCT[A/G]CAATGTGCCAGACAC	55298
rs773725769	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71967452	CCTTCTGGGTTCAAG[C/T]GATTCTTCTGCCTCA	55298
rs773733361	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71989400	GCATTAAGTTTTAAA[G/T]ATAATTCTTCTATAA	55298
rs773733561	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71972489	TGGCGCAGCCTTTTA[A/G]TGGGCATCCAATGAC	55298
rs773781665	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985814	GGCTCTGGTTTGGCC[A/G]AGCACCAGTGGCTTA	55298
rs773782153	snp	A/G	3.31417e-05	0.00407059	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982879	CCTTTGTTACCTTCC[A/G]AGCCACCCGAAAACC	55298
rs773833880	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71954465	GCATTACTGTCCTCT[C/G]CTTCACCAACATTCA	55298
rs773980863	snp	C/T	3.29478e-05	0.00405867	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987032	TGGTTCCTGCTAATC[C/T]ATAAAATCAGCTATG	55298
rs774032448	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997495	TTGGGTTTCTAGGGA[A/G]TATGGCTCAGTAGGG	55298
rs774157778	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965815	GTTTACAATCCATCA[A/G]CACAGATTTAACAGA	55298
rs774218572	snp	C/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929341	GCATTAGCCTCAAGG[C/G]TGAAGATGGAGGACA	55298
rs774266571	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949357	TGGAAAGTCGACACT[A/G]CAGTGATCTGTGATT	55298
rs774308975	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71961294	GATCGGGTGTGGTGG[C/T]TCATGTTTGTAATCC	55298
rs774327551	snp	A/C	3.3451e-05	0.00408954	intron-variant	RNF121	GRCh38.p7	11:71990549	GTAGTAATCCATAGA[A/C]GATATGTCTCAGGGT	55298
rs774362061	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71973626	ACCCCGTCTCTACTA[A/C]TAATACAAAAATTAG	55298
rs774378740	in-del	-/GT			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997206	AGAGTGCGTATGCGT[-/GT]GTGTGTGTGTGTGTG	55298
rs774380785	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71992513	CTCTTGTTTCTATCA[A/G]TTAGCCTGTGGTAAA	55298
rs774437950	snp	C/T	3.29495e-05	0.00405877	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994732	AGTTCTACAGCGAGT[C/T]GGGCATGCCTACCAA	55298
rs774453195	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969047	TCTGCCACCATGCCC[A/G]GCTAATTTTTGTATT	55298
rs774483930	in-del	-/GTGT			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997204	TAAGAGTGCGTATGC[-/GTGT]GTGTGTGTGTGTGTG	55298
rs774518691	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71957412	GGGATCTCTCTAAGT[A/G]TCTGGGTTGCTCTCT	55298
rs774663469	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71978920	TTCTAAAATTTCTGA[C/T]CATTTCAGTGTATCA	55298
rs774679815	snp	A/G	0.00955302	0.0684489	intron-variant	RNF121	GRCh38.p7	11:71957180	CTTATATTGGCAGGG[A/G]CAGTTTTAAGACAGT	55298
rs774686922	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982500	AAAGAGCTCATTGCA[A/G]TCAGCCAGCCAAGTG	55298
rs774744219	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71933272	TGAATCTGGATGTGT[C/G]CACTCTCAAGTCCTA	55298
rs774777947	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71937399	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	55298
rs774786715	snp	C/T	1.66233e-05	0.00288295	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960884	AGAGGCACCCACGCT[C/T]CTACAATGTAAGCCA	55298
rs774790508	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947939	GATTTTATAGATGTT[C/T]AGATATGATCAGCAC	55298
rs774834573	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929475	GTGAATTTCTTCAGG[A/G]GAAGGCTGGGCTTCT	55298
rs774847414	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71978675	ATAAGAACTATTATA[A/T]CAAATGCTTGTATTT	55298
rs774861475	snp	A/C	3.33812e-05	0.00408528	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996327	ATAGTGATGAAGAGC[A/C]TCAGTGGAAAACCCA	55298
rs774900248	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977564	GGGATATTGCTATTC[C/T]TGTCCCTCAGTAAAT	55298
rs774935466	snp	C/T	1.65184e-05	0.00287384	intron-variant	RNF121	GRCh38.p7	11:71987136	CTTTGTTTTTGTTTT[C/T]GCTGGAGTTTGGGGA	55298
rs775023022	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71976499	TAGCTGGGACTGCAG[C/G]TGTGCGCCACTATGC	55298
rs775044183	snp	G/T	1.64773e-05	0.00287026	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987006	CTCCTTTCCCCAGGT[G/T]GGTTTATAAGTGGTT	55298
rs775122489	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71951861	ATTGGAACCCTCACA[C/T]ACTGCTGGTGGGACT	55298
rs775148486	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71985640	ACCTTGACTTTCCTC[C/G]CTAGGGTTCAGCAGG	55298
rs775231658	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71942225	GGCATGAACCACCGT[A/G]CCCGGCAATGAAAAG	55298
rs775241035	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71969678	GTTGATCCTCCCACC[G/T]CAGCCTCCCAGGTAA	55298
rs775269754	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71945903	GGATCACTTGAACCC[A/G]GGAGTTCAAGACCAG	55298
rs775283010	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71956015	GAAAGGCCACCTTCA[A/C]TAGTGATGGGCATTT	55298
rs775366009	snp	A/G			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927392	CCCAGGCGTGGTGGC[A/G]CGTACGTAGTCCCAG	55298
rs775457915	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71951009	GTGGACGGATCACCT[A/G]AGGTCGGCAGTTTGA	55298
rs775497547	snp	A/G	0.000115417	0.00759574	intron-variant	RNF121	GRCh38.p7	11:71957298	GCCCTGCAGTCTAGG[A/G]ACTGCAGGTTAACCC	55298
rs775570137	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977933	CCATAAATGTTGCCA[C/T]GAGATGGCACTAGAG	55298
rs775584923	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71958615	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG	55298
rs775610885	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71932678	TTGAGGCTACCAAGT[-/G]GTGTCACAAAGATTT	55298
rs775615269	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71948156	AAAAATAGGAATTTG[A/G]TGGGATAGCAATTGA	55298
rs775728292	snp	C/T			upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997631	CTTCCCACCTCTTTC[C/T]CTGGGGTCCCCAGGG	55298
rs775824472	snp	A/C	1.6569e-05	0.00287824	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960876	GTGGAAGCAGAGGCA[A/C]CCACGCTCCTACAAT	55298
rs775865812	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71972103	CCTTAAAAGCATAGT[A/C]CTGAGTGGAAAAACT	55298
rs775870781	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71979563	CAAAACAAAGCAAGA[-/T]TTTTCATTCCTCATG	55298
rs775881473	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71978844	CTTTTCAGAGTTAAA[C/T]GATCTGCCTAAGTTA	55298
rs775902389	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71952982	ATGCTGTGCAATAGA[A/C]CTCAAAGAAAAAACA	55298
rs775913337	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934444	CACTAGGTTGGTAAA[C/T]CCCCAGTGGGCAGAC	55298
rs775954993	snp	C/T	1.67307e-05	0.00289224	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982896	GCCACCCGAAAACCT[C/T]TAGTACAGACAACCC	55298
rs775984045	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71954609	TCAGAAGTCTTATTT[C/G]TCTATTTTCTAGATG	55298
rs776080401	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976735	GCATATATTCCCTGG[C/T]AATTTGTGGTCAACT	55298
rs776103373	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963513	TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG	55298
rs776158393	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71962502	TGTTAGAAAACCACT[C/G]ATGTGTTATTCATTA	55298
rs776196761	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71989206	CTGCCTCAGCCTCCT[A/G]AATAGCTGGGACTAC	55298
rs776240851	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71948077	AGTTTGAGTATATGG[-/A]AAAGCTGCAGTGCAT	55298
rs776361875	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71930733	GTTTGTTAGTCATGG[C/G]CTCTCCCTTGAGACA	55298
rs776365773	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71992032	ACCAAGGTGGGAAGT[C/T]ACTTGAGCCTTGCAG	55298
rs776366840	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71975327	CCTCCTTTGAGTCTC[A/T]TCTACCTCTTTAGGC	55298
rs776462128	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71990097	AGAGGGGCATGTGGC[C/T]ACCGGAGTAATTTTC	55298
rs776504713	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71946380	TCACAAAAGATCACA[-/T]ACTCAATGAATGAAT	55298
rs776504981	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71953025	CTGAGATTTTGTACA[G/T]AATAGTACATTTTAT	55298
rs776508403	snp	A/G	4.85107e-05	0.00492473	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929147	GAGTTGAGAGACGAG[A/G]AGAGACTCAACCTGA	55298
rs776550627	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71951998	AGAAATGAAAACATA[C/T]ATTCACACAAAAATT	55298
rs776592731	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982582	TGAGGGATGAAAGGG[A/G]GGAGGAGTCAAATAT	55298
rs776631497	snp	C/T	1.65004e-05	0.00287227	intron-variant	RNF121	GRCh38.p7	11:71994697	TCTTTTCCTATCTTT[C/T]CTTCCTGCTATTCTC	55298
rs776634140	snp	A/G	1.65061e-05	0.00287277	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960860	AGCTGCTCCTGGTGC[A/G]GTGGAAGCAGAGGCA	55298
rs776737560	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71981732	CAGAAATGTGCCTCT[C/G]TCTGAGGGAGTCCTA	55298
rs776766488	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966169	GGATTACAGGCGTGC[A/G]CCACCATGCCCAGCT	55298
rs776771502	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71957916	ACCTTAGAATTTAAT[A/G]GTGAGAAAAAACCTA	55298
rs776827161	in-del	-/TT	0.000251351	0.0112077	intron-variant	RNF121	GRCh38.p7	11:71957317	GCAGGTTAACCCAGC[-/TT]AATTGAGTGATATGT	55298
rs776943188	snp	C/G	1.64977e-05	0.00287203	intron-variant	RNF121	GRCh38.p7	11:71994894	CATCTCTCCTGCAAT[C/G]TGCACACTGTAGTGA	55298
rs776946089	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71953435	ATGCGTATGGCTGTA[A/G]ATGCAATTTGTGATT	55298
rs776966283	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71956196	TTAAGTACTAAAGGA[A/G]TGGTTGTTGATTGAT	55298
rs777035800	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71979463	TCTTTTTCTTTCTCT[A/C]GATGTGACTTGATAT	55298
rs777064565	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71936066	GTTAGCCAGGACGGT[A/C]TCCATCTCCTGACTT	55298
rs777117975	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71942273	AAATGGGAGTGATGT[A/G]AGCTGATTTTCATTT	55298
rs777139205	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982381	TCCTATCCTTTGACT[A/G]TTTAAGGGTTTTAAG	55298
rs777269663	snp	A/C	3.295e-05	0.00405881	intron-variant, synonymous-codon, utr-variant-5-prime	RNF121	GRCh38.p7	11:71957263	CCAGAAGAGCAATGG[A/C]GGTAAGTGTGGTAGT	55298
rs777309887	snp	A/G	3.41454e-05	0.00413177	intron-variant	RNF121	GRCh38.p7	11:71960733	GACTTGATTCACCCC[A/G]TGTGTTTGGCTTTCA	55298
rs777402890	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979839	TTTTTTTCTCAGAGA[A/G]AACAAATGTGACCAG	55298
rs777458631	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985503	TCAGTGCAATCCCTG[A/G]AGAATAGAGCTGTGT	55298
rs777466196	snp	A/C/G			intron-variant	RNF121	GRCh38.p7	11:71960576	CCTGTATTCTATCTC[A/C/G]ACATGCCTGTCTGTT	55298
rs777483783	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994823	AGAGGGGATCATTGA[A/G]AACACGTATAGGCTG	55298
rs777515580	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71955588	AACAAACAACAACAA[A/C]AACGAAAAATAGGGA	55298
rs777530948	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71978486	TTGCTTATAACCTTA[C/T]CACTTTTCATATGTC	55298
rs777576546	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71941874	GGCAAGGTCAGATTT[A/G]TAAGGCCTTGTAGCT	55298
rs777590601	snp	C/G	1.66721e-05	0.00288717	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982788	TTTCAGATGTGGGTT[C/G]TTCCCCTCTATTTCA	55298
rs777620022	snp	A/G			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998044	CCCCACCCCCCTGTC[A/G]GGCTCAGGTGAGAAG	55298
rs777719774	in-del	-/TTTG			intron-variant	RNF121	GRCh38.p7	11:71973935	AAAGCCCTGTATTTT[-/TTTG]TTTGTTTGTTTGTTT	55298
rs777742417	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71995892	GGAACTAGGATTTAT[C/T]TCTATACCTCTCTCA	55298
rs777767496	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965158	ATGTTTATGACATCC[A/G]TTAGGTTCTGCGGCA	55298
rs777831977	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71991346	ATTCATTCAGTAGAT[-/A]CTTTTTAATGCCTGC	55298
rs777831999	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961438	TGGTGGCATGCGCCT[A/G]TAGTCTCAGCTACTG	55298
rs777834912	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954320	GTCAGGAGGCAAATA[C/T]TAAAGCCAGATCATG	55298
rs777849190	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997011	GCACCATGGATACTC[A/G]CCCGTGGGCAGGGCT	55298
rs777968408	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71937383	TGGAGTGCGACCTTG[G/T]CTCACTGCAACCTCC	55298
rs777968561	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71952505	GTGGGATACAGACTG[A/T]TGTTATAATTTATAA	55298
rs778021166	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71931227	CGTCTAGTAGTATAA[C/T]AGACTTTACAGAGTA	55298
rs778023660	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927368	TCTCTGCTAAAAATA[C/T]GAAATTTCCCCAGGC	55298
rs778058822	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963225	TTGATGAAGTTCAGT[A/G]TATCTATTTTTTAAT	55298
rs778082363	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71959454	TGGAAATTCCATGAA[C/G]ACACTATTTATGTTG	55298
rs778087939	in-del	-/TGC			intron-variant	RNF121	GRCh38.p7	11:71953475	GGGATGTAGTAGCAG[-/TGC]TTCTCAAACTTTAAT	55298
rs778169305	in-del	-/C			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926949	AAATAAAATAAAAGA[-/C]AAATAATTATACCTA	55298
rs778214871	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990430	CAAGAGGTGTTCATG[A/G]GCCATATAAAAATAG	55298
rs778260036	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71970155	TATGATTCCACTTAT[A/T]TGAGATATCTAAAGT	55298
rs778354560	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990649	CTTCTCTTCTATGGC[C/T]TCTACTATGGAGTTC	55298
rs778370862	in-del	-/T	1.66549e-05	0.00288568	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996160	CACTCCTGGCAGCTC[-/T]TGCACAGAGTCTCTT	55298
rs778387332	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71972046	TGAAATTGTTTTACA[G/T]TTAAAAGCAATACAT	55298
rs778430660	snp	C/G	1.66297e-05	0.0028835	intron-variant	RNF121	GRCh38.p7	11:71990769	CACCTCCAAATTGCT[C/G]AAGTTGATGTCACTT	55298
rs778454103	snp	G/T	1.64749e-05	0.00287005	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987090	TCATGTTTACCCTCT[G/T]TGGTCTTAACTTATT	55298
rs778463198	snp	G/T	1.64727e-05	0.00286986	intron-variant, missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71994805	CTTTGTGGACGTCAG[G/T]GAAGAGGGGATCATT	55298
rs778480541	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71938528	TTCTCCATGTTGGTC[A/T]GGCTGGTCTCGAACT	55298
rs778485535	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934219	TAGTCCTCAAACTTC[C/T]GAAACGTCTGTGTGC	55298
rs778490482	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71948800	GGAGTTGGGGAAGAA[G/T]GTGAATGAGAGGAGA	55298
rs778503905	snp	A/C	1.70101e-05	0.00291629	intron-variant	RNF121	GRCh38.p7	11:71960939	TCAGTCATCAAGAGA[A/C]CCTTCCTAAGTATTC	55298
rs778504554	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929368	GACAGAGAGAGAGGT[C/T]GGAGGGGTGGGGGTG	55298
rs778568751	snp	C/T	9.68945e-05	0.00695973	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929099	AGGTTGGAGGTGGTG[C/T]TGCTGGGGAACGGGA	55298
rs778666353	snp	C/G/T			intron-variant	RNF121	GRCh38.p7	11:71967611	TTTGTATTTTTAGTA[C/G/T]GTGGTTTCACCATGT	55298
rs778751958	snp	A/G					GRCh38.p7	11:71975947	GTGGTAAGGATTACT[A/G]TGTGTAGGTGTGATA	55298
rs778827395	snp	C/G	1.64944e-05	0.00287175	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960849	GGTGGTGGCCCAGCT[C/G]CTCCTGGTGCAGTGG	55298
rs778843083	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71971925	GGGGATATGTAAGAG[C/G]GTGTTCACTGAAGTG	55298
rs778886419	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71940273	GTTAGAAAAATAAGA[C/T]ATGTAGTCCAGTTGG	55298
rs778943177	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71954110	CTTACCTAATTAGCT[A/G]CCTGAGCTTTGGACA	55298
rs778975745	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71966348	TTATCGAAGTAATAC[A/G]TACCATAGTTTTAAA	55298
rs779079554	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71985142	GAGTTTCCTAGGCTG[A/G]TCTCGAACTCCTGAG	55298
rs779111234	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71944781	GTAGACTGAGTAATA[-/G]GAAGGAAGGAAAAGA	55298
rs779113678	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71960565	GGTCCGTAGAGCCTG[C/T]ATTCTATCTCGACAT	55298
rs779135208	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938802	CAGGGGAGCTCATGT[A/G]TAGGTTAATTTGGTT	55298
rs779191955	snp	C/T	1.73249e-05	0.00294315	intron-variant	RNF121	GRCh38.p7	11:71982949	GGAAGAGCCCAGGTT[C/T]TCCGAAGCTAATGGG	55298
rs779213379	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71949105	GGTTGGGCTTATTCC[G/T]CTTTAATGTTTTGTG	55298
rs779297267	snp	C/G	1.64754e-05	0.00287009	intron-variant, missense, utr-variant-5-prime	RNF121	GRCh38.p7	11:71957239	CAGGTTGATATGTCA[C/G]ATCTCTCTCCAGAAG	55298
rs779330877	snp	A/T			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997160	CGTGCCAGCGGTCAC[A/T]CTGCCACATCACTTC	55298
rs779343873	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71960697	TGGAAAGCACTGTCC[C/G]TTTATCACTACAGCA	55298
rs779352290	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71964798	AAGCTGTGTTTTAGT[A/T]CAAGTTAGCAACCTG	55298
rs779362122	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71991757	TATGGCCAAGAAGTG[C/G]CTGGAGAAGTAGTGA	55298
rs779393135	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71959592	CCCACACATTCTGAT[A/G]TATTTGATTTTCTCT	55298
rs779450730	in-del	-/TTTT			intron-variant	RNF121	GRCh38.p7	11:71984747	CCACACCCGGCTAAT[-/TTTT]TTTTTTTTTTTTTTT	55298
rs779474275	in-del	-/A			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927524	GACACCGTTTCAAAG[-/A]AAAAAAAAAAAGCAC	55298
rs779477582	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71972864	TCCATAACTTAGGAG[C/T]TCAAGCCCAACCTTC	55298
rs779522244	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71991969	CAAAAAAAAAAAAAA[A/C]CTAGCCGGGCGTGGT	55298
rs779535922	snp	A/G	1.64868e-05	0.00287109	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982832	CTGGTGGAGGTTCCT[A/G]GTGATCTGGATCTTG	55298
rs779552869	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71988896	CTTTCTTCTAGGGGT[A/G]GTACAGGCTGAAGGA	55298
rs779620531	in-del	-/TGT			intron-variant	RNF121	GRCh38.p7	11:71972288	AGACTCCCCGGAGAA[-/TGT]TGTGTAAAGGAAAGG	55298
rs779652745	snp	C/G	1.64798e-05	0.00287047	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990621	AGAAGATGCCATGGA[C/G]TTTGGCATCTCCCTT	55298
rs779660406	snp	C/T	0.000269614	0.0116075	intron-variant	RNF121	GRCh38.p7	11:71995569	ATCCTTTATTGGGGT[C/T]GTTGTTGGGAGTGGG	55298
rs779672627	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71945438	TGCAATATCATCCCC[A/C]CTGTTTGTTCAAGAG	55298
rs779681891	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71957782	CAACTCTGCAACTAA[A/C]TTGTTTTGTAAATAG	55298
rs779732584	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937132	GTCATCGGCACTGCT[C/T]TCTGCTCCCGTAGCG	55298
rs779765755	in-del	-/CTTTA			intron-variant	RNF121	GRCh38.p7	11:71992416	AAAAGTGTTTTGAGT[-/CTTTA]CTTAAGAGACAATTT	55298
rs779784994	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71931510	CCCCAGCTGTTTCTT[G/T]GCAGCCTTAGCTTGT	55298
rs779801989	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71964540	GTGGTGCAGTATGGC[A/G]ATTTCGGCTCACTGC	55298
rs779889078	snp	A/G/T	0.000148405	0.00861289	missense, nc-transcript-variant, utr-variant-5-prime, stop-gained	RNF121	GRCh38.p7	11:71960841	GCAACCTTGGTGGTG[A/G/T]CCCAGCTGCTCCTGG	55298
rs779892715	in-del	-/TTTTTTTTTT			intron-variant	RNF121	GRCh38.p7	11:71984756	GGCTAATTTTTTTTT[-/TTTTTTTTTT]TTTTTTGTCTATTTT	55298
rs779901233	in-del	-/AAATG			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926913	TCAAAAAATGAAATA[-/AAATG]AAATAAAATAAAATA	55298
rs779915940	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71990218	AGAGACAGCTCAGCA[A/T]GGCAGCTCACTTAGT	55298
rs779917554	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71932612	TATTAGTATTCCCTA[G/T]TTGTGATTGAGGAAG	55298
rs779922569	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71963450	ACATGGTGAAACCCC[A/G]TCTCTAATAAAAATA	55298
rs779942557	snp	A/G	8.24817e-05	0.00642137	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982816	TCACAGTGAAGCTGC[A/G]CTGGTGGAGGTTCCT	55298
rs779966531	snp	C/T	1.70621e-05	0.00292074	intron-variant	RNF121	GRCh38.p7	11:71995414	GCTGGAGTGCCGCCC[C/T]GGCTCTCACCATTTC	55298
rs779969765	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71954513	TAGTAGTTTTAAAAT[-/A]ATGTCCACTTTGCCA	55298
rs779973203	snp	A/G	1.66624e-05	0.00288633	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960890	ACCCACGCTCCTACA[A/G]TGTAAGCCACTTTGC	55298
rs780011830	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942181	CTAATAATCCATCTG[C/T]CTCGACCTCCCAAAG	55298
rs780018072	snp	G/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928847	TCATTTTCCAAGAAC[G/T]CTCCCTTGCTGAAGC	55298
rs780075221	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71941495	CAAGACAACTGAGGT[C/T]CTTGCTCATATTAGG	55298
rs780201061	snp	G/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929574	TCCACTAGTAGTATA[G/T]CTTTGAGTTATCTTA	55298
rs780253436	snp	A/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927632	GAGAACACAAGCTAA[A/T]TCTAATTCATAATAG	55298
rs780267503	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71981118	CAGTGGTGTGATCTC[A/G]GCTCCCTGCAAGCTC	55298
rs780274121	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71984285	ATAGTAACTACTAGC[-/T]TTTTTTTTTGAGATG	55298
rs780333625	snp	C/T	9.60753e-05	0.00693025	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929072	TGAAGATGGCGGCAG[C/T]GGTGGAGGTGGAGGT	55298
rs780345042	snp	G/T	0.00153787	0.027687	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928631	CACTACAACTCTTTC[G/T]TGGAGGGAGCGGAAT	55298
rs780359657	snp	A/G	1.71167e-05	0.00292542	intron-variant	RNF121	GRCh38.p7	11:71982934	AGAGTTTAAGTAGTG[A/G]GAAGAGCCCAGGTTT	55298
rs780386171	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71968433	GCCCATCTTGCTGTT[C/T]CTGATTTTCTATCCT	55298
rs780458574	snp	A/G	3.31724e-05	0.00407248	intron-variant	RNF121	GRCh38.p7	11:71990761	CTTCTTGACACCTCC[A/G]AATTGCTCAAGTTGA	55298
rs780481653	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71985360	TACAAAGAAAATCAC[C/T]TCTCTTGTCTCAAAG	55298
rs780505242	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71980157	TCAGACTGTTTTAGA[A/G]TGCTTCATTCAGAGA	55298
rs780563124	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71994513	CTGGTCACTTCTCCC[C/T]ATCTGCCCAGCAAAG	55298
rs780574366	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71939513	ATGATTTTGTGGGGT[A/G]TTCTGGGTCAAGTTA	55298
rs780576769	snp	A/G	1.65119e-05	0.00287327	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996286	ATTGGTGTAGTCCAA[A/G]GCATCAACTACATCC	55298
rs780660279	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71966695	GCTCTCACTATATTG[C/T]CCAGGCTGGTCTTGA	55298
rs780678847	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71962093	CTGCCTCGGCTTCCC[A/G]CATAGCTGGGACTAC	55298
rs780784992	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71990333	GTTAGGGGAGGCAAG[A/G]ACTAAGAGCAGAGTG	55298
rs780793577	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71934938	AGTGTTCCAAATGCA[-/TT]TTCTTTTTTTTTTTT	55298
rs780872273	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997315	GGATTCCCAGTCCAG[A/G]GAATATCCCTACATG	55298
rs780878064	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71931555	AATCCGTCTTTAATA[C/T]GTAATTATGGGGTCT	55298
rs780894617	snp	G/T	1.69481e-05	0.00291098	intron-variant	RNF121	GRCh38.p7	11:71960744	CCCCATGTGTTTGGC[G/T]TTCAGGGTCGAGCAC	55298
rs780937066	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71954168	GGCCCCAAATGAATA[A/C]ACTCCTTAATGAGGG	55298
rs780940688	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71951639	AAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA	55298
rs780975178	snp	A/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71997997	GGGGCTGGTCAGAGG[A/T]CCTAGGGATCACCCT	55298
rs780997113	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71978414	CCTCAAATCCTTGGT[G/T]TGTGTCTTCTGATAA	55298
rs781059381	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71965498	TGATCCATCCACCTC[A/G]GCCTCCCAAAGTGCT	55298
rs781068333	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71983863	AAAGTCTTTCAAATT[A/G]TAGATTGCTCTTCTT	55298
rs781070814	snp	A/G	1.64958e-05	0.00287187	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996268	GCCTGGCAGCCTGTC[A/G]TCATTGGTGTAGTCC	55298
rs781101501	in-del	-/AC			intron-variant	RNF121	GRCh38.p7	11:71950015	CAAAAACAAAACAGA[-/AC]ACACACACACACACA	55298
rs781101522	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71950535	GTTGCAGTGAACCGA[A/G]ATCATGCCATCGCAC	55298
rs781104698	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71961046	AGTGTATTGGCGAGT[A/G]TGTGTCTAAGGGTCA	55298
rs781148111	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71933816	AGGCACCCAATAAGT[A/G]TTTGATAATCGTTGT	55298
rs781224663	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975812	TAAGTTTACTTTGTG[C/T]TCCTCTGAAAGATAA	55298
rs781388744	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71969857	CAGGCATGAGCCACC[A/G]TGCCAAGCCAAAACC	55298
rs781441390	snp	A/G			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929201	TATCGGGAGGTGGGG[A/G]TCTTAGGAGAGAAGG	55298
rs781517476	in-del	-/AGA			intron-variant	RNF121	GRCh38.p7	11:71944697	CAGCATTAGGACACC[-/AGA]AGATTTGAACTTGGG	55298
rs781549233	snp	C/G	4.94735e-05	0.00497336	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990607	TGCAGGATCAAACCA[C/G]AAGATGCCATGGACT	55298
rs781635986	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71982207	CACACGTGGTGGCAC[A/G]CGCCTGTAATCCCAG	55298
rs781673023	in-del	-/TG			intron-variant	RNF121	GRCh38.p7	11:71993311	AACATTTTCACTGTC[-/TG]TAATTCCAAAATTTT	55298
rs781696765	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71968587	GAGGAGAAGCAGAGC[A/G]TAAATATAGTTGGGA	55298
rs781701590	in-del	-/AATA	1.64874e-05	0.00287113	intron-variant	RNF121	GRCh38.p7	11:71994705	ATCTTTCCTTCCTGC[-/AATA]TATTCTCCTTCAGTT	55298
rs781731769	snp	A/G	0.00111421	0.0235767	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928537	CTGCTGTTTTTGAAA[A/G]TGAGTCCTACCGAGG	55298
rs781779261	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71951717	CAAATGGCCAAAGAA[C/T]ACATGAAAAGAAGTC	55298
rs796076712	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71973679	GTAATCCCAGCTACT[-/G]TGGAGGCTGAGGCAG	55298
rs796082356	snp	A/G			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997369	CCTGGGCCTGACAAC[A/G]GGAGTGGTGGGTGGG	55298
rs796109408	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942422	GGGGGTGTTTTAGTC[C/T]TTTTGGGCTGCTATA	55298
rs796115463	in-del	-/AT			intron-variant	RNF121	GRCh38.p7	11:71934938	AAGTGTTCCAAATGC[-/AT]TCTTTTTTTTTTTTT	55298
rs796247928	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71940113	TGTATAAAGGAATAA[A/G]GACATGAAGTCTCTA	55298
rs796277505	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71945655	CTAGTTCTCTGAAAT[A/G]CAAAGAAGAATACGA	55298
rs796302776	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71941237	GGAGCGAGATGATGC[A/G]GACCTGAGCTTGAGC	55298
rs796312687	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979840	TTTTTTCTCAGAGAG[A/G]ACAAATGTGACCAGA	55298
rs796402086	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71959853	GTTGGCCAGGCTCAT[C/T]GTTAACTCCTGACCT	55298
rs796413689	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71966882	TTTGTTTTTTTTTTT[-/T]GAGACGGAATCTCAC	55298
rs796415075	in-del	-/TTTT			intron-variant	RNF121	GRCh38.p7	11:71992841	ATATTTCTATTTTTT[-/TTTT]CAGAATGGAAATATA	55298
rs796430460	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71962057	ACTGCAAGCTCCGCC[-/T]CCCGGGTTCACGCCA	55298
rs796443345	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71976216	CTTATGGCCTGCTGT[C/T]TTATGGCCATGCTTA	55298
rs796453334	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71986254	GACTAACCGGGCCCA[C/G]GTACAAACAACCTGT	55298
rs796474265	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967376	TTTTTTTGAGACGGA[A/G]TCTCACTCTGTCACC	55298
rs796481168	snp	C/T			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930282	AGATCTCTGAGGGGT[C/T]AGAATCTTAGAGGCC	55298
rs796522442	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71956396	ATTATTCTAGAGCAG[G/T]GGTTTTCAACTAGGG	55298
rs796525542	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71964646	CAGCACCAGGCTAAT[A/T]TTTTGTATTTTTGGT	55298
rs796528429	in-del	-/AG			intron-variant	RNF121	GRCh38.p7	11:71938098	TTGTCCTCCTTTCAC[-/AG]AGTGTTATCAATAAC	55298
rs796549104	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976270	GTGGCCCCAAGCCCT[A/G]ATCCTAGGGTCCCAG	55298
rs796579287	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71967874	CAGCTTGAGCCATAT[G/T]ATATATTTGGTACAT	55298
rs796681507	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71982439	TGTTCGAGATACCAT[G/T]CTGGCACTCCTCAAA	55298
rs796727722	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927929	ACTTTTCTAGACGTT[C/T]TGTGGGCTCACAGGC	55298
rs796763226	in-del	-/AA			intron-variant	RNF121	GRCh38.p7	11:71948538	AAAAAAAAAAAAAAA[-/AA]GCTTATCAACTCAGC	55298
rs796795893	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71991198	TGTAACAAACCTGCA[C/T]ATGTACCCTCTGAAT	55298
rs796817108	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71958483	TTGTCTCATTGTCAG[A/G]ACTGTCTTTAATAGT	55298
rs796824713	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71936834	TTTTAATGCTTTAAT[G/T]CAGGGACTATTTTTC	55298
rs796874147	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71975418	ATCCTGGAACACCCA[C/T]CATGATGCCTTTTTC	55298
rs796973743	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71971227	ATCTCTACAAAAAAT[-/A]AAAAAAATTAGCCAG	55298
rs796992454	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71947276	ACTTTGGGAGGCCAG[C/T]GCCGGAGGATCACTT	55298

Page 1 | 2