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
rs947932	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71945659	TGAGTCGTATTCTTC[C/T]TTGTATTTCAGAGAA	55298
rs1055452	snp	C/T	0.215446	0.2476	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996419	AAAGACTCAAAGGGG[C/T]GCTTGGGCCACTCAG	55298
rs1541306	snp	C/T	0.383053	0.211653	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996967	TGTCCCAAAACAAAT[C/T]TTCAATGAATTCTGA	55298
rs1892920	snp	C/T	0.211819	0.247067			GRCh38.p7	11:71991385	tttgtaattctggca[C/T]atagctatgtgtcta	55298
rs1892921	snp	C/T	0.284733	0.247575			GRCh38.p7	11:71991092	agatagtttttcaac[C/T]gttgtccccactccc	55298
rs1939240	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997733	CCTAGGGATGTCAGC[A/C/T]GGGGAACAGCTGGGA	55298
rs1939241	snp	C/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71994083	ggaggccaaggaggg[C/T]ggatcacgaggtcag	55298
rs2032352	snp	A/G	0.137867	0.223442	intron-variant	RNF121	GRCh38.p7	11:71932912	CCCCTTTTCAGGAGG[A/G]ATGATTAGCCTGTTG	55298
rs2155141	snp	C/G	0.321769	0.239477	intron-variant	RNF121	GRCh38.p7	11:71931530	CGGATTTCACCTGCT[C/G]TTTCACAAGCTAAGG	55298
rs2155142	snp	C/T	0.184521	0.241273	intron-variant	RNF121	GRCh38.p7	11:71931478	GACATTAGTAGAAAC[C/T]TGAATACCAACTAAG	55298
rs2187496	snp	C/G	0.390464	0.206809	intron-variant	RNF121	GRCh38.p7	11:71940915	gctggaccactcact[C/G]ttccttacctcactg	55298
rs2276383	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71990486	AAGGCCCAAAGGCTA[A/G]AGCAAGTGCGGGCAA	55298
rs2276384	snp	C/T	0.211212	0.246973	intron-variant	RNF121	GRCh38.p7	11:71990477	AGGCTAGAGCAAGTG[C/T]GGGCAAACTATGACC	55298
rs2276385	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71990456	AACTATGACCAAATC[C/G]AGTCTGCTGTCTATT	55298
rs2363736	snp	A/T	0.382666	0.211895	intron-variant	RNF121	GRCh38.p7	11:71945921	agttcaagaccagct[A/T]gggcaacatagagaa	55298
rs2363737	snp	A/G	0.212122	0.247114	intron-variant	RNF121	GRCh38.p7	11:71946117	ctctgccttaaaaaa[A/G]aaaagaaaagaaaag	55298
rs2885880	snp	A/G	0.382279	0.212137	intron-variant	RNF121	GRCh38.p7	11:71944801	GAAGGAAAAGATAGT[A/G]GATATATTTCTTACC	55298
rs3216157	in-del	-/A	1.76426e-05	0.00297001	intron-variant	RNF121	GRCh38.p7	11:71957317	CATATCACTCAATTA[-/A]GCTGGGTTAACCTGC	55298
rs3750914	snp	A/C	0.0930568	0.194599	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927995	CTGTAGCCCCAGCTC[A/C]CACGCCTCTGGGCGT	55298
rs3814722	snp	A/C	0.00597247	0.0543191	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997482	TATTCCCTAGAAACC[A/C]AATGCCGAAGGCCCA	55298
rs3829215	snp	A/G	0.184203	0.241186	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996443	CAGTCCGACACAGCC[A/G]GAGGGGTCCTGAGTG	55298
rs3841467	in-del	-/AC	0.272511	0.248984	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997204	CACACACACACACAC[-/AC]GCATACGCACTCTTA	55298
rs3886589	snp	G/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71958441	TAGGTCTAATGGACT[G/T]AAGCTATAAGAAGAT	55298
rs3887002	snp	C/T	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71970597	GGCCCAGGAGTTTAA[C/T]GCTTCAGTAAACTAT	55298
rs3898386	snp	C/T	0.0337553	0.125452	intron-variant	RNF121	GRCh38.p7	11:71975360	ATTTCTCACACCTTC[C/T]TCAAATACTAGTTGT	55298
rs3915628	snp	C/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71971567	AGATTAATATTtatc[C/T]agagaaactcctaca	55298
rs4121395	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71958196	GCATATTAAAAAGAT[C/T]TTTAACTGGATCATG	55298
rs4121396	snp	A/C	0	0	intron-variant	RNF121	GRCh38.p7	11:71958394	TGGGAAAGAAGAGTC[A/C]ATATGTCCTTTGTTG	55298
rs4399349	snp	C/T	0.213333	0.247296	intron-variant	RNF121	GRCh38.p7	11:71944327	AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAG	55298
rs4479013	snp	C/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71962686	AACTTAAACTCATAT[C/G]TTTAGAAAATAAGAA	55298
rs4491255	snp	G/T	0.407158	0.194426	intron-variant	RNF121	GRCh38.p7	11:71973575	gcagatcacctgagg[G/T]tgggagttcaagacc	55298
rs4944232	snp	C/T	0.283947	0.247685	intron-variant	RNF121	GRCh38.p7	11:71931212	TGAAGGACTTGAGAG[C/T]GTCTAGTAGTATAAT	55298
rs4944242	snp	G/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71956095	CAGTAGTAGAATGAA[G/T]TTCTACCTGTGTTAC	55298
rs4944243	snp	C/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71963308	ggtcatagagattac[C/T]cttatgttttctttg	55298
rs4945353	snp	C/T	0.283684	0.24772	intron-variant	RNF121	GRCh38.p7	11:71930993	ATGCACCACCACGCC[C/T]GGCTGATTTTTTGTA	55298
rs4945378	snp	A/G	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71957820	CATCATATATCTTAT[A/G]ATGATTGCTCATCAG	55298
rs4945382	snp	A/T	0.216649	0.247765	intron-variant	RNF121	GRCh38.p7	11:71962886	cactccgtttttttt[A/T]aaattttatttatta	55298
rs4945391	snp	A/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71981438	TGTTGTTGTTTTTTT[A/T]AAAAATATTCTTTGA	55298
rs4945392	snp	C/T	0.215446	0.2476	intron-variant	RNF121	GRCh38.p7	11:71983599	GTAATTTAATATCTG[C/T]ACTCAACAGAAAAAG	55298
rs5743655	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997858	CTGAGGACAGTGTCC[C/T]GCCACCACCTGCCTT	55298
rs5743656	snp	A/G	0.0337553	0.125452	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997914	TTCTCTTCCCCAGCT[A/G]TGGCTTCCCATGGTA	55298
rs5743657	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998091	CAAAGCTCTTTTCAT[A/G]TGTAACAGTTCTGAG	55298
rs5792563	in-del	-/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71948946	GCTGAACCTACCAGG[-/T]TTCATGAGCTAGCTA	55298
rs5792564	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71950421	AACCCTGTCTCTACT[-/A]AAAAATACAAAAATT	55298
rs5792566	in-del	-/A	0.470908	0.117046	intron-variant	RNF121	GRCh38.p7	11:71991236	TTATTAAAAAAAAAA[-/A]TTAGCCAGATCTCAG	55298
rs6592447	snp	A/T	0.211516	0.24702	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930047	GACTGGTGTATTAAA[A/T]TACCAGTGGTCCTTG	55298
rs6592448	snp	C/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71958998	TGTTTTTAAGTGTGC[C/T]CTACCCTCTTAGCCT	55298
rs6592449	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71959176	TTTCTGTCAGATTCT[C/T]CCACCCAGGGTAAAG	55298
rs6592450	snp	C/T	0.383053	0.211653	intron-variant	RNF121	GRCh38.p7	11:71960120	TCTCTAGTTACTAAA[C/T]TTCCTTGAGCCTTTG	55298
rs6592451	snp	A/G	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71963891	tctgttcttttgcag[A/G]taccacattgttatg	55298
rs6592452	snp	A/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71968330	CTCGCAAAGTGCTGG[A/G]ATGACAGGTGTGAGC	55298
rs6592453	snp	C/G	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71972185	AGAAAGCAATAAACA[C/G]TTTGCATGAACAGGT	55298
rs6592455	snp	A/G	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71978495	ACCTTATCACTTTTC[A/G]TATGTCAGTTATTTT	55298
rs7102192	snp	A/G	0.322483	0.239262	intron-variant	RNF121	GRCh38.p7	11:71937123	TATCAGTGAGTCATC[A/G]GCACTGCTTTCTGCT	55298
rs7102523	snp	C/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71987872	TGTGAGGGAATGAGA[C/T]GACACAGATGGGTGT	55298
rs7102639	snp	A/C/G	0.040671	0.13668	intron-variant	RNF121	GRCh38.p7	11:71958034	GGTGATTTTAAGCTT[A/C/G]GTATGAACCAGTTGT	55298
rs7103210	snp	C/G	0.357451	0.225731	intron-variant	RNF121	GRCh38.p7	11:71937920	CCTCTACTCCTCAGA[C/G]AAAAATCTGTAGGTA	55298
rs7106653	snp	A/G	0.215446	0.2476	intron-variant	RNF121	GRCh38.p7	11:71964800	GCTGTGTTTTAGTAC[A/G]AGTTAGCAACCTGTC	55298
rs7106730	snp	A/G	0.184521	0.241273	intron-variant	RNF121	GRCh38.p7	11:71938306	CATTTTACGTGTGTA[A/G]TCTCTTAATTTTTTT	55298
rs7106748	snp	A/C	0.283947	0.247685	intron-variant	RNF121	GRCh38.p7	11:71934757	GTAAACAGTGGGTTC[A/C]TATTCTAGACTagga	55298
rs7108458	snp	G/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71976837	ggtttcattttgtgg[G/T]tttgattcttcattt	55298
rs7113436	snp	A/T	0.215144	0.247558	intron-variant	RNF121	GRCh38.p7	11:71978553	TTGTATGTGTGACTT[A/T]ATGCATTTTTAATCA	55298
rs7113520	snp	A/G	0.212122	0.247114	intron-variant	RNF121	GRCh38.p7	11:71980900	tgagatattttgtat[A/G]tattggaataaataa	55298
rs7114081	snp	A/T	0.0581099	0.160244	intron-variant	RNF121	GRCh38.p7	11:71993301	cagtgttctgcaaca[A/T]tttcactgtctaatt	55298
rs7114483	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71950773	ttcccctgcctcagc[C/G]tccccagtagctggg	55298
rs7115513	snp	A/T	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71953449	AGATGCAATTTGTGA[A/T]TGTGAGTGCTGGGAT	55298
rs7121080	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71992889	CTGTTTATAAAAGTA[A/G]TATGTTCTCTTTGTA	55298
rs7121260	snp	A/G	0.357877	0.225527	intron-variant	RNF121	GRCh38.p7	11:71989520	TGGTGTAAGATCAAT[A/G]ATTTCTAGTGAGTTA	55298
rs7121292	snp	A/C	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71964701	ctaggctggtctcgc[A/C]ctcctgaactcaagc	55298
rs7123536	snp	C/T	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71939947	TAGAGTTATAAATTA[C/T]GTACAAGATGCCACA	55298
rs7124429	snp	G/T	0.0581099	0.160244	intron-variant	RNF121	GRCh38.p7	11:71993095	GAAAACAGTACATTG[G/T]ATCACTTTATTGACA	55298
rs7125718	snp	C/T	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71993380	actcattaccccttc[C/T]cacagccctggttta	55298
rs7126394	snp	A/G	0.215144	0.247558	intron-variant	RNF121	GRCh38.p7	11:71974383	ACCTACTCTGTTATA[A/G]CACTTATAATGAATT	55298
rs7128317	snp	A/G	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71990321	TCATTGTCACCAGTT[A/G]GGGGAGGCAAGGACT	55298
rs7128346	snp	A/G	0.32955	0.237006	intron-variant	RNF121	GRCh38.p7	11:71966205	tgtatttttagtaga[A/G]acagggtttctccac	55298
rs7128974	snp	C/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71965986	tcatttggcttcttt[C/G]aattatttgttcata	55298
rs7130215	snp	C/G	0.0622301	0.165053	intron-variant	RNF121	GRCh38.p7	11:71936904	GCACATAGCCCATAT[C/G]CATATATTTATTGAG	55298
rs7131230	snp	C/T	0.366885	0.220993	intron-variant	RNF121	GRCh38.p7	11:71990115	CGGAGTAATTTTCAG[C/T]CTCTGCACCAGTGAC	55298
rs7924516	snp	C/T	0.284995	0.247539	intron-variant	RNF121	GRCh38.p7	11:71956943	TTACGTCTGTCTTTC[C/T]CACTAGTCTGTGAGC	55298
rs7924834	snp	A/G	0.21695	0.247806	intron-variant	RNF121	GRCh38.p7	11:71933287	CCACTCTCAAGTCCT[A/G]TTTATCTGCCAAAAT	55298
rs7925196	snp	A/G	0.0599851	0.162463	intron-variant	RNF121	GRCh38.p7	11:71967167	tgagccaccgcgccc[A/G]gccAATATTTGTGTT	55298
rs7925411	snp	G/T	0.218151	0.247963	intron-variant	RNF121	GRCh38.p7	11:71967340	gtaataattATGTGG[G/T]ttttttttgtttttt	55298
rs7925604	snp	A/G	0.211516	0.24702	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930210	CATGCCAGCATATGG[A/G]CAAAGACATCACAGG	55298
rs7925901	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71967072	gagacggggtttcac[C/T]ttgttagccaggatg	55298
rs7926550	snp	C/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71985164	actcctgagctcaaa[C/G]aatcctcccacttca	55298
rs7929479	snp	C/T	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71981583	GGGAGTTAGGAGGCA[C/T]TGGAGAGAAGACTAG	55298
rs7931163	snp	A/G	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71986684	tgaggcagaagaatc[A/G]cttgaactcaggagg	55298
rs7931941	snp	C/T	0.408188	0.193589	intron-variant	RNF121	GRCh38.p7	11:71956558	GATGGCTAGTGATAT[C/T]GCTAGTTAATAGCAG	55298
rs7932163	snp	A/T	0.0600199	0.162504	intron-variant	RNF121	GRCh38.p7	11:71970818	AGCAACTACCAAGAC[A/T]GGGACTTACCTTGCC	55298
rs7932263	snp	A/G	0.0584853	0.160693	intron-variant	RNF121	GRCh38.p7	11:71940736	tgaggtaaaccagac[A/G]tgggaacagatggtt	55298
rs7937408	snp	A/G	0.184838	0.241358	intron-variant	RNF121	GRCh38.p7	11:71966904	gaatctcactctgtc[A/G]cccaggccggactgc	55298
rs7938496	snp	A/G	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71984632	gggtctcactctgtc[A/G]cccaggctggagtgc	55298
rs7939435	snp	A/G	0.0240643	0.107019	intron-variant	RNF121	GRCh38.p7	11:71949345	attgcttaggcctgg[A/G]aagtcgacactgcag	55298
rs7940392	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71967017	gctgggactacaggc[A/G]cccgccaccgcgccc	55298
rs7942626	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71992803	ATGGGTAAATTAACA[A/G]CCAATCTGAGAAACG	55298
rs7943227	snp	A/G	0.38286	0.211774	intron-variant	RNF121	GRCh38.p7	11:71959675	GAATCTCATTCTGTC[A/G]CCCAGGACGGAGTGC	55298
rs7945374	snp	A/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71985497	TTGTGATCAGTGCAA[A/T]CCCTGGAGAATAGAG	55298
rs7945535	snp	C/T	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71970473	ccagacaagcttggg[C/T]aatgcagggagaccc	55298
rs7948821	snp	A/G	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71941439	ATACTTGTGACTTCA[A/G]tgtcaaacatttttc	55298
rs7949480	snp	C/T	0.284471	0.247612	intron-variant	RNF121	GRCh38.p7	11:71986542	GGAGGCTGAGGCGAG[C/T]GGATCATGTGGTCAG	55298
rs7951194	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71966912	ctctgtcacccaggc[C/T]ggactgcggactgca	55298
rs7951564	snp	A/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71945160	ACTTGGCTAATTTTT[A/T]AATTTTTTGTAGAGA	55298
rs8181566	snp	C/G	0.0267878	0.112589	intron-variant	RNF121	GRCh38.p7	11:71934834	cttagaagcctgtgt[C/G]gagaaggattctgag	55298
rs10501408	snp	A/G	0.211516	0.24702	intron-variant	RNF121	GRCh38.p7	11:71969544	TTATCACACATATAC[A/G]TAATTTTAAAACATA	55298
rs10532049	in-del	-/TG			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997215	ATGCGTGTGTGTGTG[-/TG]TGTGTGTGTGTACGT	55298
rs10635678	in-del	-/AAAAA			intron-variant	RNF121	GRCh38.p7	11:71982350	CAAGACTCCATCTCA[-/AAAAA]AAAAAAAAAAAAAAA	55298
rs10654699	in-del	-/TTTG/TTTGTTTG	0.379686	0.22972	intron-variant	RNF121	GRCh38.p7	11:71989070	TCTGCATTATGGTTT[-/TTTG/TTTGTTTG]TTTTGTTTGTTTGTT	55298
rs10671705	in-del	-/A/AAG/AGA/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71936409	CTTTTTTATTTTTTA[-/A/AAG/AGA/G]GACAGAGTCTCGCTC	55298
rs10686485	in-del	-/T/TT/TTT	0.441021	0.161279	intron-variant	RNF121	GRCh38.p7	11:71968888	TTTTTTTTTTTTTTT[-/T/TT/TTT]GAGTCAGGCTCTTGC	55298
rs10707525	in-del	-/T	0.307423	0.243316	intron-variant	RNF121	GRCh38.p7	11:71965272	ATGACTGCATAGTAA[-/T]TTTTTTTTTTTTTTT	55298
rs10736780	snp	C/T	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71939195	AGGTGTGAGCCACTG[C/T]CCCTGGCTCATCTAA	55298
rs10736781	snp	C/T	0.407845	0.193868	intron-variant	RNF121	GRCh38.p7	11:71939322	CTTAGGCACACTTAC[C/T]GACTCCACAGTTGGA	55298
rs10736782	snp	A/G	0.407158	0.194426	intron-variant	RNF121	GRCh38.p7	11:71942966	GCAGAAGGGACACAC[A/G]GCCTCCCTAAAGCCA	55298
rs10736783	snp	A/G	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71943097	AGGTTAGGTTTCAAC[A/G]TACTAATTTTGGGGA	55298
rs10751188	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71943084	ACTATTGCATTGGAG[A/G]TTAGGTTTCAACGTA	55298
rs10751189	snp	C/G	0.383053	0.211653	intron-variant	RNF121	GRCh38.p7	11:71959532	AAGCTTATGACTCAA[C/G]TTACATTTGTATTTG	55298
rs10751190	snp	C/T	0.284733	0.247575	intron-variant	RNF121	GRCh38.p7	11:71969711	GGGACCACAGGTGTG[C/T]ACCACCCTTGCCTGG	55298
rs10751191	snp	C/T	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71969874	GCCAAGCCAAAACCA[C/T]ATTTTAAAAAGCAAG	55298
rs10751192	snp	C/T	0.184838	0.241358	intron-variant	RNF121	GRCh38.p7	11:71970107	aaccttgaagacatg[C/T]taagtgaaataagcc	55298
rs10793011	snp	C/T	0.243061	0.249904	intron-variant	RNF121	GRCh38.p7	11:71956415	TTTCAACTAGGGGGA[C/T]GCTATGGCAATATAC	55298
rs10793012	snp	A/G	0.0566069	0.158427	intron-variant	RNF121	GRCh38.p7	11:71974237	TGAGCCACCACGCCC[A/G]GCCAAGCCCTGTTGT	55298
rs10793013	snp	A/C	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71984480	TAGAGACAGGGTTTC[A/C]CCGTGTTAGCCAGGA	55298
rs10793014	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71987792	AAATTGACTTAGAAG[A/G]ATACAAAATAAATAA	55298
rs10793015	snp	C/T	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71989862	TTTTATCTTTTTTTC[C/T]TAAACCTGTGTTTGA	55298
rs10898812	snp	A/G	0.215747	0.247642	intron-variant	RNF121	GRCh38.p7	11:71987755	TCTACCTACATGACC[A/G]TGGTTGGCTACAGCT	55298
rs11235407	snp	G/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929953	TAAGTGTCTCTCTCT[G/T]CTTCTGGATTTATGA	55298
rs11235408	snp	A/C	0.401037	0.199218	intron-variant	RNF121	GRCh38.p7	11:71937387	gtgcgaccttggctc[A/C]ctgcaacctccgcct	55298
rs11235409	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71939123	tagccaggctgatct[C/T]gaactcctgatctca	55298
rs11235411	snp	A/G	0.0240643	0.107019	intron-variant	RNF121	GRCh38.p7	11:71976989	GTGCTGTCCACAGTT[A/G]GGAGGTTCTTTGTGT	55298
rs11235412	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71979711	TCACATTCCTCCTCA[A/G]AACATGCTATTGATG	55298
rs11235413	snp	A/G	0.0185938	0.0946107	intron-variant	RNF121	GRCh38.p7	11:71984328	GTCGCCCAGGCTGGA[A/G]TGCAGTGGCACGATC	55298
rs11235414	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71986602	gaaaccccgtctcta[C/G]taaaaaaaatataaa	55298
rs11235415	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71986765	cagagcgagactctc[A/T]tctcaaaaaaaaaaa	55298
rs11235416	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996773	TATAGAAGAGCTAAC[A/G]TACTCAGGCTTGTGC	55298
rs11315989	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71986789	AAAAAAAAAAAAAAA[-/A]GAAAAAAAATACAAA	55298
rs11332543	in-del	-/A	0.322245	0.239334	intron-variant	RNF121	GRCh38.p7	11:71974669	TTGTCAATTTCTGCC[-/A]TAGTCAGAAGTTTTT	55298
rs11366662	in-del	-/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71980351	CCTGTAAAATGACAC[-/T]TTTTTTTTTTTAAGA	55298
rs11376874	snp	A/G	0.188951	0.242431	intron-variant	RNF121	GRCh38.p7	11:71936831	ATATTTTAATGCTTT[A/G]ATGCAGGGACTATTT	55298
rs11377249	in-del	-/T	0.401457	0.237349	intron-variant	RNF121	GRCh38.p7	11:71968068	GATCTTTTTTTTTTT[-/T]AAGATGAAGTCCTGC	55298
rs11398516	in-del	-/A	0.219049	0.248077	intron-variant	RNF121	GRCh38.p7	11:71945798	CAACTCATCAATAAT[-/A]AAAAAAAATAACCTA	55298
rs11399586	in-del	-/T	0.499722	0.0117779	intron-variant	RNF121	GRCh38.p7	11:71961966	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC	55298
rs11433118	in-del	-/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71967350	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC	55298
rs11602419	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71942809	atatatatgtacaca[A/C]acacacacacacaca	55298
rs11605115	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71982258	agagaatcgcttaaa[A/C]ctgggaggcagaggc	55298
rs11819828	snp	A/G	0.0360663	0.129354	intron-variant	RNF121	GRCh38.p7	11:71994383	AATGGCTTGCCTGAC[A/G]CAGCTTTTGATCACC	55298
rs11826336	snp	A/G	0.0633504	0.166319	intron-variant	RNF121	GRCh38.p7	11:71971134	catgcctgtaatccc[A/G]gcactttgggaggct	55298
rs12099319	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967401	gtcacccaggctgga[A/G]tgcaatggcatggtc	55298
rs12226658	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71962043	tgcaatctctgctca[A/C]tgcaagctccgcctc	55298
rs12279363	snp	C/T	0.00953873	0.0683987	intron-variant	RNF121	GRCh38.p7	11:71943352	agttggaaatacgag[C/T]ttatagctcagggag	55298
rs12282197	snp	A/G	0.0839998	0.186933	intron-variant	RNF121	GRCh38.p7	11:71941016	gtatgactggaattt[A/G]ggttaaacgtaaggg	55298
rs12286617	snp	A/C	0	0	intron-variant	RNF121	GRCh38.p7	11:71977144	ATCTCTACCTTTATT[A/C]TACTACTTGGGCTTA	55298
rs12288772	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990231	CAAGGCAGCTCACTT[A/G]GTGTCCAGAAGTTAC	55298
rs12290168	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71984742	tgccgccacacccgg[C/G]taatttttttttttt	55298
rs12292971	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71982331	acagagcaagactcc[A/T]tctcaaaaaaaaaaa	55298
rs12360732	snp	G/T	0.166758	0.235735	intron-variant	RNF121	GRCh38.p7	11:71948737	TGGTGGCCTGAAAGG[G/T]GAGGTTTCCACTTCA	55298
rs12787981	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71984567	ttacaggcatgagcc[A/C]ccgtgcctggccAGT	55298
rs12790314	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71942811	atatatgtacacaca[A/C]acacacacacacata	55298
rs12805158	snp	G/T	0.00477324	0.0486193	intron-variant	RNF121	GRCh38.p7	11:71948624	CTGTAGCAGCTGTTA[G/T]AGCCAACATCTACTT	55298
rs12806517	snp	A/C	0	0	intron-variant	RNF121	GRCh38.p7	11:71990249	GTCCAGAAGTTACCA[A/C]CAGTGGAGTCCCCAC	55298
rs12807090	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71948517	gaaactgtctccaaa[A/C]aaaaaaaaaaaaaaa	55298
rs17161719	snp	G/T	0.188951	0.242431	intron-variant	RNF121	GRCh38.p7	11:71936830	AATATTTTAATGCTT[G/T]AATGCAGGGACTATT	55298
rs17161725	snp	A/G	0.040671	0.13668	intron-variant	RNF121	GRCh38.p7	11:71940479	GGAATGAACGCCCAA[A/G]GTCAATGTTGAGAAA	55298
rs17161751	snp	A/G	0.209084	0.246629	intron-variant	RNF121	GRCh38.p7	11:71977301	CTGTGGACTGGAAAG[A/G]CACCTGATGCACAGG	55298
rs17161758	snp	A/G	0.0391387	0.134304	intron-variant	RNF121	GRCh38.p7	11:71986203	CACATCATTTCTTTC[A/G]TTTTTGGCCTGTGGA	55298
rs28395798	snp	C/T	0.0215028	0.101435	upstream-variant-2KB, downstream-variant-500B, utr-variant-5-prime	IL18BP, RNF121	GRCh38.p7	11:71998040	TTCCCCCCACCCCCC[C/T]GTCAGGCTCAGGTGA	55298
rs33992126	in-del	-/T	0.386694	0.20932	intron-variant	RNF121	GRCh38.p7	11:71981215	CGGCTAATTTTTTTT[-/T]GTATTTTTAGTAGAG	55298
rs34075366	snp	A/G	0.125432	0.216755	missense, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71995498	CGTGGGAAAGAAGCA[A/G]ACGTGTCCCTACTGC	55298
rs34308211	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977722	GAATCATCCAGAGCT[C/T]TGCCTCTTCCAGGAA	55298
rs34319979	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71980831	TGATTTCAAAGCCTT[-/G]AGTACCAAAAAAAGT	55298
rs34395072	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71956100	TAGAATGAATTTCTA[-/C]CCTGTGTTACTATTT	55298
rs34428026	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71934961	TTTTTTTTTTTTTTT[-/TT]AGACAGTCTTGCTCT	55298
rs34454915	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71933565	ATGGATTCAACAGAA[-/C]CCCTAAGGTGCTTGA	55298
rs34596006	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71989564	ATAAGCAAATGCAGC[-/T]TTTGTATATAAATAT	55298
rs34611451	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71995052	ACAACCTGGCTGGGT[-/A]CTGAGAGGAACCTGA	55298
rs34646174	in-del	-/C			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996579	GGAGCATAGGAATTG[-/C]CCCCCTCCAGGCTTC	55298
rs34733327	in-del	-/AAG	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71936408	ACTTTTTTATTTTTT[-/AAG]AGACAGAGTCTCGCT	55298
rs34778760	in-del	-/TT/TTT/TTTT			intron-variant	RNF121	GRCh38.p7	11:71946867	CAGGTGCTCTGGCTC[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT	55298
rs34830792	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71971791	GCCAAGTGTTGGCAA[-/G]GGATCAAAGGCTGTA	55298
rs34870190	in-del	-/TTTG			intron-variant	RNF121	GRCh38.p7	11:71989091	TGTTTGTTTGTTTGT[-/TTTG]TTGTTTGTTTTGAGA	55298
rs34947570	in-del	-/A			utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996338	AGCATCAGTGGAAAA[-/A]CCCACCCCACACGCC	55298
rs34961303	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71936831	TATTTTAATGCTTTA[-/G]ATGCAGGGACTATTT	55298
rs34966470	snp	A/G	0.018048	0.0932645	synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71990705	TGCAGACTACATGGC[A/G]TCTACCATAGGGGTA	55298
rs34974965	in-del	-/AGAG	0.0566069	0.158427	intron-variant	RNF121	GRCh38.p7	11:71964440	CATCTGAGAGTAGAG[-/AGAG]TTTCACTTCTTCTTT	55298
rs35077599	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71960951	GACCCTTCCTAAGTA[-/T]TTCTAGGTCCCAGCC	55298
rs35167855	in-del	-/A	0.427879	0.175668	intron-variant	RNF121	GRCh38.p7	11:71947483	CTCAAAAAAAAAAAA[-/A]GGAATTGGGCAGTGA	55298
rs35229588	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71939614	TGTTATCTTAATTTT[-/C]CCAGATGAGAAAAAC	55298
rs35238262	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71992322	GCTTTACCAAAAATT[-/G]GGGGAAGCTTTCATA	55298
rs35334153	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71937888	TCTTTATGTTTTCCC[-/T]TTGAAGTCATTTGCT	55298
rs35417249	snp	C/T	9.92064e-05	0.00704225	missense, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71995483	CCGTGGCTGGTGCAT[C/T]GTGGGAAAGAAGCAA	55298
rs35441591	in-del	-/C			intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929357	GAAGATGGAGGACAG[-/C]AGAGAGAGGTCGGAG	55298
rs35483977	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71932475	ACTATTTGTGCTCTA[-/G]GGGGTGGGAACTTTA	55298
rs35525269	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71949875	GCGTGGTGGCACGTA[-/C]CCTGTAATCCCAACT	55298
rs35553015	in-del	-/T	0.391397	0.206172	intron-variant	RNF121	GRCh38.p7	11:71941950	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC	55298
rs35566006	in-del	-/AA/AAA	0.28052	0.24813	intron-variant	RNF121	GRCh38.p7	11:71951209	TCAAAAAAAAAAAAA[-/AA/AAA]TGCAATAATGAAAGT	55298
rs35648557	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71936836	TAATGCTTTAATGCA[-/G]GGGACTATTTTTCTC	55298
rs35678632	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71955413	TTCTATCAAGCACCC[-/A]AAATGATGCTGATAC	55298
rs35709836	in-del	-/A	0.381697	0.212499	intron-variant	RNF121	GRCh38.p7	11:71984938	GCACTTTTTAAAAAT[-/A]AGAGATGAGGTCGCA	55298
rs35710756	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71976373	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	55298
rs35712258	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71974573	TGACCATTAAATTGG[-/C]AGAGTTGGACCTAAA	55298
rs35794524	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71934939	AGTGTTCCAAATGCA[-/TT]CTTTTTTTTTTTTTT	55298
rs35844388	snp	A/G	0.0648734	0.168012	synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71990717	GGCATCTACCATAGG[A/G]GTAAGTTCATCCGGG	55298
rs35970528	in-del	-/A	0.490836	0.0670685	intron-variant	RNF121	GRCh38.p7	11:71988640	AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA	55298
rs35972144	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71961307	GCTCATGTTTGTAAT[-/C]CCTAGTACTTTGGGA	55298
rs36036687	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71936482	CAAGTTCCGCCTCCT[-/G]GGGTTCACACCATTC	55298
rs36125406	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71975438	TGCCTTTTTCTATCT[-/G]GGACCTATTGGCCAT	55298
rs55669226	in-del	-/G	0.407845	0.193868	intron-variant	RNF121	GRCh38.p7	11:71930543	ACCTCCCAATCACTA[-/G]AGACTACAGGTGTTT	55298
rs55673306	snp	A/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71967875	AGCTTGAGCCATATG[A/T]TATATTTGGTACATT	55298
rs55724289	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71979618	TTTGTCCAACTCAGA[A/G]TAGAATCCAGGATCT	55298
rs56097487	snp	A/G	0.381308	0.21274	intron-variant	RNF121	GRCh38.p7	11:71976495	CGAGTAGCTGGGACT[A/G]CAGGTGTGCGCCACT	55298
rs56134788	in-del	-/TTTT	0	0	intron-variant	RNF121	GRCh38.p7	11:71984767	TTTTTTTTTTTTTTT[-/TTTT]GTCTATTTTTAGTAG	55298
rs56160537	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71987670	ATAAAGACCATATGG[A/G]CTACAAAACCTAAAA	55298
rs56168103	in-del	-/TCTCTG	0	0	intron-variant	RNF121	GRCh38.p7	11:71993478	ATATTTGTCCCTTTG[-/TCTCTG]GCTTTTTTCACTTAG	55298
rs56304359	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71978650	TTATACATATTACTT[C/T]CATTTAAATATAAGA	55298
rs56409948	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948900	CCACAGTATCTGAAC[C/G]CCACCAGATAGAGAC	55298
rs56857710	snp	A/C			upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928630	TCACTACAACTCTTT[A/C]GTGGAGGGAGCGGAA	55298
rs56891737	snp	A/G	0.0584853	0.160693	intron-variant	RNF121	GRCh38.p7	11:71931106	CCCAAATGTGCTGGG[A/G]TTACAGGTGTGAGTC	55298
rs56950003	in-del	-/AACACA			intron-variant	RNF121	GRCh38.p7	11:71942808	ATATATATGTACACA[-/AACACA]CACACACACACACAC	55298
rs57198333	snp	A/G	0.0607341	0.163335	intron-variant	RNF121	GRCh38.p7	11:71977205	CAGCCAGGTATGGTG[A/G]GAGGGTGATCCCTAG	55298
rs57475283	in-del	-/T/TTT/TTTT	0.625	0.125	intron-variant	RNF121	GRCh38.p7	11:71938337	TTTTTTTTTTTTTTT[-/T/TTT/TTTT]GAGACAGAGTTTCGC	55298
rs57550396	in-del	-/T/TTT	0	0	intron-variant	RNF121	GRCh38.p7	11:71961985	TTTTTTTTTTTTTTT[-/T/TTT]GAGACAGAGTCTCGC	55298
rs57683667	snp	G/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71988297	CAGTGAGTCAATGAG[G/T]CAGATGAGGGTGGAA	55298
rs57734644	in-del	-/CACA			intron-variant	RNF121	GRCh38.p7	11:71950033	ACACACACACACACA[-/CACA]AAACTCGCACAAAAA	55298
rs57824459	in-del	-/C	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71980143	CTTTTTATGTAAGGT[-/C]AGACTGTTTTAGAAT	55298
rs57945872	in-del	-/GTTT	0	0	intron-variant	RNF121	GRCh38.p7	11:71989101	TTTGTTTGTTTGTTT[-/GTTT]TGAGATGGAGTCTTG	55298
rs58101667	in-del	-/AG/GA	0	0	intron-variant	RNF121	GRCh38.p7	11:71942788	ATATATATATATATA[-/AG/GA]TAGATATATATATGT	55298
rs58109845	snp	A/T	0.0603597	0.1629	intron-variant	RNF121	GRCh38.p7	11:71966567	GCTCACTGCAGCCTC[A/T]AACACCTGGGCCCAG	55298
rs58408933	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71985214	TTCCAGGTGTGAGCC[A/G]TTGTGCCTGCCCTCA	55298
rs58510802	snp	A/G	0.0244538	0.107838	intron-variant	RNF121	GRCh38.p7	11:71952287	CTATAGATAGAGACA[A/G]AATGTAAATTAGTGG	55298
rs58524951	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71948539	AAAAAAAAAAAAAAA[-/A]GCTTATCAACTCAGC	55298
rs58694482	in-del	-/TTTTTTTTT			intron-variant	RNF121	GRCh38.p7	11:71984762	TTTTTTTTTTTTTTT[-/TTTTTTTTT]GTCTATTTTTAGTAG	55298
rs58923802	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71955873	CCTGAGTCAGGGCAC[A/C]TGAATAAATTCTGTG	55298
rs59848440	in-del	-/TTTT	0.263401	0.249641	intron-variant	RNF121	GRCh38.p7	11:71992835	AAGTAAATATTTCTA[-/TTTT]TTTTTTCAGAATGGA	55298
rs60162352	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938503	TTTGCATTTTTAGTA[A/G]AGACGTGGTTTCTCC	55298
rs60170713	snp	A/C	0.0197687	0.0974348	intron-variant	RNF121	GRCh38.p7	11:71951294	GGCATAGAGAGAGGT[A/C]CCCTATTCATTGACA	55298
rs60435912	snp	C/T	0.0162398	0.0886349	intron-variant	RNF121	GRCh38.p7	11:71993114	ACTTTATTGACAGTT[C/T]ATTAGGTTCCTTTTT	55298
rs60446177	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71938632	CCTTAATTCTTCTAA[A/G]AAACCTTTTATTTGA	55298
rs60840528	snp	C/T	0.0599851	0.162463	intron-variant	RNF121	GRCh38.p7	11:71936615	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG	55298
rs61051812	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	LOC100133315, RNF121	GRCh38.p7	11:71926712	TTGAGACCAGCCTGG[C/G]CAACATGGTGAAACC	55298
rs61174237	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71944272	TAGGAGGTGGAGGTT[A/G]CAGTGAGCCGAGATT	55298
rs61495563	in-del	-/T/TT	0.625	0.125	intron-variant	RNF121	GRCh38.p7	11:71968903	TTTTTTTTTTTTTTT[-/T/TT]GAGTCAGGCTCTTGC	55298
rs61537950	snp	C/T	0.00194043	0.0310878	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929025	GCGGAAGCAGCTGGC[C/T]CGCGCGGGGACTGCG	55298
rs61749189	snp	A/G	0.0188638	0.0952682	intron-variant, synonymous-codon, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71957259	CTCTCCAGAAGAGCA[A/G]TGGAGGTAAGTGTGG	55298
rs61890882	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71934692	CTGGATTTTTTTTAG[G/T]CATGTAAAATGAGTG	55298
rs61890883	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71949520	AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGT	55298
rs61890884	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71955246	AGACAAGCTGTTAGA[C/T]CACTTAGAAAGGATG	55298
rs61890885	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71963616	AGAGCAAGACTCCTT[A/C]CCAAAAAAAAAAGAG	55298
rs61890894	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71982642	TGGAGTTAACTTTAT[C/T]CAAAGTTGTAAATAC	55298
rs61890895	snp	A/C	0.0558544	0.157504	intron-variant	RNF121	GRCh38.p7	11:71995712	CCTGCCCCCATGATA[A/C]AACCCCAGTTTCCCT	55298
rs63735061	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71934942	GTTCCAAATGCATTC[G/T]TTTTTTTTTTTTTTT	55298
rs67525256	in-del	-/TGTCTC			intron-variant	RNF121	GRCh38.p7	11:71993477	AATATTTGTCCCTTT[-/TGTCTC]GGCTTTTTTCACTTA	55298
rs71052836	in-del	-/GTGTGT	0	0	intron-variant	RNF121	GRCh38.p7	11:71942823	TATATACATATATAT[-/GTGTGT]GTGTGTGTGTGTGTT	55298
rs71052837	in-del	-/AA	0	0	intron-variant	RNF121	GRCh38.p7	11:71946887	GAGCGATACTGTCTC[-/AA]AAAAAAAAAAAAAAA	55298
rs71466344	snp	C/T	0.357877	0.225527	intron-variant	RNF121	GRCh38.p7	11:71934939	AGTGTTCCAAATGCA[C/T]TCTTTTTTTTTTTTT	55298
rs71467457	in-del	-/TAAAA	0.5	0	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926942	TAAAATAAAATAAAA[-/TAAAA]GACAAATAATTATAC	55298
rs71467458	multinucleotide-polymorphism	AG/TA	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71937439	TGCCTCAGCTTCTGG[AG/TA]TAGCTGGGATTACAG	55298
rs71467459	in-del	-/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71962017	TGTCGCCCAGGCGGG[-/G]AGTGCAGTGGTGCAA	55298
rs71477706	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71930924	CACAACCTCTGCCTT[C/T]TGGGTTCAAACAATT	55298
rs71958930	in-del	-/TTT			intron-variant	RNF121	GRCh38.p7	11:71938335	TTTTTTTTTTTTTTT[-/TTT]TTGAGACAGAGTTTC	55298
rs72477716	snp	A/C	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71974266	GTTTTGAGTAAGGTC[A/C]TACTGTATCTAAATT	55298
rs72521507	in-del	-/G	0.211819	0.247067	intron-variant	RNF121	GRCh38.p7	11:71936830	ATATTTTAATGCTTT[-/G]AATGCAGGGACTATT	55298
rs72952249	snp	C/T	0.0103295	0.0711199	intron-variant	RNF121	GRCh38.p7	11:71961090	GTGAAAAGGATAGAA[C/T]ATAAGACTATGTTCA	55298
rs72956138	snp	C/T	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71975878	GATTTTTCAGGTCAG[C/T]ATCAGGAAAGAGCTG	55298
rs72956140	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71977917	TGAACCAAATGTGTC[C/T]CCATAAATGTTGCCA	55298
rs72956144	snp	C/T	0.0588605	0.161139	intron-variant	RNF121	GRCh38.p7	11:71979195	TACAGAGCTAGTTGA[C/T]AGAAACTTAGCCTGT	55298
rs72956152	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71988523	TAAAAATAAATCCTG[G/T]CCAGGTGTGGTGGCT	55298
rs72956164	snp	A/G	0.0509478	0.151255	intron-variant	RNF121	GRCh38.p7	11:71992437	TTAAGAGACAATTTG[A/G]TGTCTCTTAAATAGA	55298
rs73527765	snp	A/G	0.0283406	0.115616	intron-variant	RNF121	GRCh38.p7	11:71933993	TGGCTCTAGCACTCT[A/G]TGTACTGTTTCTAAT	55298
rs73529832	snp	A/G	0.0248432	0.108648	intron-variant	RNF121	GRCh38.p7	11:71940978	TAAACAGCGTGGAAT[A/G]TTCTGGGACTGTACG	55298
rs73529869	snp	G/T	0.0225045	0.103662	intron-variant	RNF121	GRCh38.p7	11:71963830	ATTGATCAAAGATAT[G/T]TTGGCTTATTTTTGT	55298
rs73529872	snp	A/G	0.0248432	0.108648	intron-variant	RNF121	GRCh38.p7	11:71965628	TAACAGTTTATCACA[A/G]TTGCAAGCAACAATT	55298
rs73529874	snp	A/G	0.0248432	0.108648	intron-variant	RNF121	GRCh38.p7	11:71966405	AAGCAAAACACATTG[A/G]TCCCCTGCCCAACTC	55298
rs73531941	snp	G/T	0.0225045	0.103662	intron-variant	RNF121	GRCh38.p7	11:71972061	GTTAAAAGCAATACA[G/T]TAAGTACCTGTAGGA	55298
rs73531952	snp	C/T	0.282632	0.247861	intron-variant	RNF121	GRCh38.p7	11:71976604	ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	55298
rs73531955	snp	A/C	0.212728	0.247206	intron-variant	RNF121	GRCh38.p7	11:71976748	GGCAATTTGTGGTCA[A/C]CTGAAACCCCTAAGC	55298
rs73531963	snp	A/G	0.0248432	0.108648	intron-variant	RNF121	GRCh38.p7	11:71987198	AAGTCGTGGTTATTA[A/G]CAGGAGGGACGTAAT	55298
rs73531984	snp	C/T	0.0248432	0.108648	intron-variant	RNF121	GRCh38.p7	11:71993575	CATTGTGTGTGACAC[C/T]GCATTTGGTTTATTC	55298
rs74236639	snp	A/T	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71935591	TCATTCCTATATCCT[A/T]TGTGCCTGGCATAGA	55298
rs74236643	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71965580	TAGATCTCAAATAAA[A/G]TTTAATTTACCTTTA	55298
rs74236644	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71970859	CTATAAGAATAGACA[A/G]ACAGATCAGTGGGAC	55298
rs74319588	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71942303	TTTTAAAAGATCTTT[C/T]TGGCTGCTTTGAGAA	55298
rs74322193	snp	G/T	0.0376037	0.131863	intron-variant	RNF121	GRCh38.p7	11:71965613	GATTGACTTGTTAAT[G/T]AACAGTTTATCACAG	55298
rs74328773	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71981067	TTCTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT	55298
rs74387290	snp	A/T	0.0205511	0.0992634	intron-variant	RNF121	GRCh38.p7	11:71962866	TCAAGACTTCTTACT[A/T]CTTTCACTCCGTTTT	55298
rs74411661	snp	C/T	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71933278	TGGATGTGTCCACTC[C/T]CAAGTCCTATTTATC	55298
rs74427665	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71938529	TCACCGTGTTAGCCA[A/G]GATGGTCTCGATCTG	55298
rs74432654	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71955488	ATGCTGGAGAAAGGC[A/G]GAGGACCAAATTCCC	55298
rs74546937	snp	G/T	0.0763149	0.179815	intron-variant	RNF121	GRCh38.p7	11:71935490	CATTATGTACATTTG[G/T]GTCTTCCTTTCCGGA	55298
rs74571183	snp	G/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71942423	GGGGTGTTTTAGTCC[G/T]TTTGGGCTGCTATAG	55298
rs74642895	snp	C/T	0.357877	0.225527	intron-variant	RNF121	GRCh38.p7	11:71934941	TGTTCCAAATGCATT[C/T]TTTTTTTTTTTTTTT	55298
rs74712916	snp	A/G	0.0599851	0.162463	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929610	GGAACTGTTTTATTT[A/G]TCGTTCCATTCTAAG	55298
rs74828536	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71973334	CCAATCTCTTAAAAA[A/G]GAAAAAATTAGCTGG	55298
rs74828900	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71966881	TTTTGTTTTTTTTTT[G/T]TGAGACGGAATCTCA	55298
rs74847531	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71979241	TTTGAAAAATCAAGC[C/T]AATCCCTTCCTCCAA	55298
rs74853873	snp	A/C	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71944332	AGCGAGACTCTGTCT[A/C]AAAAAAAAAGAGGAA	55298
rs74854624	snp	A/C	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71977229	TCCCTAGCTTACAAC[A/C]TGAGGGGATGCAGAG	55298
rs74925573	snp	A/C	0.0763149	0.179815	intron-variant	RNF121	GRCh38.p7	11:71934609	AGAGATTTTTGGTCC[A/C]AGCCAATATCTTACT	55298
rs74983801	snp	A/G	0.0154538	0.0865337	intron-variant	RNF121	GRCh38.p7	11:71944558	GGAGCTGGGAGCAGA[A/G]GAAGGTAAAACTGGA	55298
rs75087014	snp	A/C	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71948516	TGAAACTGTCTCCAA[A/C]AAAAAAAAAAAAAAA	55298
rs75117483	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71993476	ACAATATTTGTCCCT[C/T]TGGCTTTTTTCACTT	55298
rs75133815	snp	A/T	0.0611083	0.163768	intron-variant	RNF121	GRCh38.p7	11:71976328	AGACCTGCTGCCCCC[A/T]CCATTCTGGGTATAT	55298
rs75193665	snp	A/C	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71949409	GGCGACAGAGTGAGA[A/C]CCTGTCTCAAAAAAA	55298
rs75208362	snp	A/T	0.040671	0.13668	intron-variant	RNF121	GRCh38.p7	11:71930609	GAAATGACCTCCAAG[A/T]CCCCTTCTAGCTTTT	55298
rs75281208	snp	A/G	0.0341408	0.126114	intron-variant	RNF121	GRCh38.p7	11:71995051	TTACAACCTGGCTGG[A/G]TCTGAGAGGAACCTG	55298
rs75287892	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71941952	TTTTTTTTTTTTTTG[A/G]GACGGAGTCTTGCTC	55298
rs75429718	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71992689	TAGGTTTCAAAGCTG[A/G]GATTTCTGATTCGGC	55298
rs75572933	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71959654	TTTTTTTTTTTTTTT[G/T]AGATGGAATCTCATT	55298
rs75605544	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71945081	CAGTCTGAACCTCCT[A/G]GGCTCAAGTGATCCT	55298
rs75638532	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71950644	TATACCTCACCACAC[C/T]AAAGGCATCTTACTT	55298
rs75700850	snp	G/T	0.0584853	0.160693	intron-variant	RNF121	GRCh38.p7	11:71942933	AAAGGGGGCTCCTTG[G/T]TGCTGTGTCTTCACA	55298
rs75718282	snp	C/T	0.0349115	0.127424	intron-variant	RNF121	GRCh38.p7	11:71956987	AGGATTCTTGTCCTC[C/T]TCTGCCCTTATTGCC	55298
rs75763230	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71958460	CTATAAGAAGATAGA[-/T]TTTTTTTTTGTCTCA	55298
rs75779997	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71958919	CACATCCGTTCACTG[A/G]TATGTTGTCTGAGAA	55298
rs75800455	snp	G/T	0.0168055	0.0901129	intron-variant	RNF121	GRCh38.p7	11:71960211	AAGCAGTCCAGACTT[G/T]TTAGGCTTTAACTAG	55298
rs75813068	snp	C/G	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71960434	AAATGGGCAATGATG[C/G]AGGTTTCTCCTGGGA	55298
rs75822536	snp	A/G	0.0520825	0.152737	intron-variant	RNF121	GRCh38.p7	11:71994468	CAGTTTATAGGTTCT[A/G]TTACATCTAACTTCC	55298
rs75845526	snp	A/G	0.093417	0.194889	intron-variant	RNF121	GRCh38.p7	11:71966001	CAATTATTTGTTCAT[A/G]TCATTGACTAGATTT	55298
rs75918152	snp	G/T	0.375	0.216506	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927718	GTTTAACTTTTATTG[G/T]ATTATCTAGCTTTTA	55298
rs75951882	snp	A/G	0.0185938	0.0946107	intron-variant	RNF121	GRCh38.p7	11:71952969	AACAGTATTAACCAT[A/G]CTGTGCAATAGAACT	55298
rs76143084	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71981066	TTTCTTTTTTTTTTT[G/T]GAGATGGAGTCTTGC	55298
rs76230847	snp	C/T	0.093417	0.194889	intron-variant	RNF121	GRCh38.p7	11:71980377	TAAGATGGAGTCTAA[C/T]ACTCTGTCACCTAGG	55298
rs76394075	snp	A/G	0.0479149	0.147179	intron-variant	RNF121	GRCh38.p7	11:71961635	AGAAAACAAATAGCA[A/G]AATGGCAGAAGTTAA	55298
rs76397783	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71941175	TTTTGGAAGGATCAG[A/G]TTGGAAAAAGGAGAA	55298
rs76430787	snp	A/G	0.077417	0.180873	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997154	GTGACACGTGCCAGC[A/G]GTCACTCTGCCACAT	55298
rs76458573	snp	A/G	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71938299	AAGTAAGCATTTTAC[A/G]TGTGTAGTCTCTTAA	55298
rs76609923	snp	C/T	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71934118	AGCTTGCTTGGCTTC[C/T]TGGACTATTCCGATC	55298
rs76706957	snp	G/T	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71934013	CTGTTTCTAATTACT[G/T]CCGGGCTTTGTTGGT	55298
rs76732256	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71987818	AATAATAGAGCAGAG[C/T]GGTGTCTGCAAGTCT	55298
rs76757342	snp	C/T	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71940945	CAAAATGAAAAGATA[C/T]GCAAGGCTTGGAGAC	55298
rs76766472	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71944459	ATCCAGGCAAGTAGG[A/G]CTTCCAAATTTATCT	55298
rs76905273	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71946428	AGATAAGGTCTTGCC[A/G]TGTTGCCCAGGCTGG	55298
rs76950159	snp	C/T	0.0862618	0.188932	intron-variant	RNF121	GRCh38.p7	11:71995409	CTGGGGCTGGAGTGC[C/T]GCCCTGGCTCTCACC	55298
rs76978892	snp	A/G	0.0528381	0.153711	intron-variant	RNF121	GRCh38.p7	11:71933148	CTAACCAACCTCTGA[A/G]AGGAATTAGATGCAC	55298
rs77045688	snp	C/T	0.0984431	0.198823	intron-variant	RNF121	GRCh38.p7	11:71974805	CAGCCTCTCCAGATT[C/T]CCCCACAAACTCAGT	55298
rs77110075	snp	C/T	0.0170251	0.090679	intron-variant	RNF121	GRCh38.p7	11:71934570	TTTAGTAAATGTTCC[C/T]TGTTGCCAGAGATTT	55298
rs77221646	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942302	TTTTTAAAAGATCTT[C/G/T]CTGGCTGCTTTGAGA	55298
rs77256982	snp	C/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71952170	AGTACATGCTACAAA[C/G]TGGATGAACCTTGAA	55298
rs77294058	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974177	CAATCTCCTGACCTC[A/C/G]TGATCCACCCTCCTC	55298
rs77453107	snp	A/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71984748	CACACCCGGCTAATT[A/T]TTTTTTTTTTTTTTT	55298
rs77480741	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71952116	AACGTGGTATTTATA[C/T]GATGGAATATTCTTT	55298
rs77585300	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71946665	TTTTTTTTTTTTTTA[A/G]AGTGACGGAAATGAT	55298
rs77683492	snp	A/G	0.0930568	0.194599	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927450	CGTTTGAACCCAGTA[A/G]GCGGAGGCTGCAGTG	55298
rs77708273	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957718	TTATTATCCATGATA[C/T]AGGATGGGGAGCTCT	55298
rs77713910	snp	A/G	0.0170251	0.090679	intron-variant	RNF121	GRCh38.p7	11:71972130	AACTAAGAAACAGAA[A/G]GATGTGTAACACAAT	55298
rs77759376	snp	A/G	0.0185938	0.0946107	intron-variant	RNF121	GRCh38.p7	11:71987494	CATGAATGGCCTTAC[A/G]TTCAACTAGGCCAGG	55298
rs77811421	snp	C/G	0.0919752	0.193722	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929704	TAAATGATTGTATGC[C/G]GGAATTCATGCATTT	55298
rs77822402	snp	A/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71994585	AGTTTAAAAAAAAAA[A/G]GATGTCCTCTAACTC	55298
rs77882289	snp	G/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71946662	GTTTTTTTTTTTTTT[G/T]TAGAGTGACGGAAAT	55298
rs77912446	snp	A/C	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71971396	TCAAAATAAATAAGT[A/C]AATGAACTTTTTTAA	55298
rs77916164	snp	C/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71981595	GCATTGGAGAGAAGA[C/T]TAGCGATGACTTCAA	55298
rs77964153	snp	C/T	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71955437	CTGATACTGCCAGTC[C/T]ATGGGCTACACTTTG	55298
rs77988220	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71956875	AGGTTAAAAGGCAAG[A/G]CACCTCTTTGTTCTA	55298
rs77996546	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71964252	CTTATTCCTAAGTAT[A/G]TTATTCTTTTTGATG	55298
rs77999297	snp	A/C	0.0599851	0.162463	intron-variant	RNF121	GRCh38.p7	11:71960399	CTTTCTCGTTCCAGC[A/C]TCAGGTTGAAATAGA	55298
rs78057754	snp	G/T	0.00049478	0.0157209	missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime	RNF121, LOC100133315	GRCh38.p7	11:71929121	GGAACGGGAGCTGGA[G/T]GAGGTAAGCGGAGTT	55298
rs78115570	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71988172	GATGGAATTTTGGCT[A/G]TTGCTTCAGTTGTCA	55298
rs78170050	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71956828	CCTCCATAAAGCCTT[C/T]CCTAGTCTAAAACAC	55298
rs78207798	snp	A/C	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71935415	AGTGCTTGTGCTGTT[A/C]ACCACAACGGGCAAT	55298
rs78236537	snp	A/G	0.0418186	0.138422	intron-variant	RNF121	GRCh38.p7	11:71952859	TAAATCAAGCTAGTA[A/G]CTTATCGATCACCTC	55298
rs78249973	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71966882	TTTGTTTTTTTTTTT[G/T]GAGACGGAATCTCAC	55298
rs78267463	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71939872	TCTCTGCTCTAAAGA[A/G]GTTATGGTCTAGTTG	55298
rs78302642	snp	A/C/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71930754	CCTTGAGACAATTAC[A/C/G]TATATCTCAAAGCTG	55298
rs78379377	snp	C/T	0.00755907	0.0610114	intron-variant	RNF121	GRCh38.p7	11:71937661	TGGATTAGATTCTTA[C/T]TTCTGTATTGCTTCA	55298
rs78411223	snp	A/G	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71931847	TATTGCCCCCTGTGT[A/G]GCACTTTCTGTTTTA	55298
rs78448866	snp	C/T	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71957635	AAAATCTTAGAAGAG[C/T]GCCTGGCATGTGGTA	55298
rs78483610	snp	A/G	0.00189292	0.0307063	intron-variant	RNF121	GRCh38.p7	11:71957282	AAGTGTGGTAGTTCG[A/G]GCCCTGCAGTCTAGG	55298
rs78636878	snp	C/T	0.0520825	0.152737	intron-variant	RNF121	GRCh38.p7	11:71990000	CTACCCTGTCCCACC[C/T]TCTTTGCCTGGGGAA	55298
rs78708286	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71960646	CAGCTATGAAGCAGG[C/G]AATGTGTTCTGAGCT	55298
rs78725368	snp	C/T	0.0930568	0.194599	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927474	TGCAGTGAGCCCAGA[C/T]TGAACCAGTGCATTC	55298
rs78736687	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71995700	TGAGCTGCTAGTCCT[A/G]CCCCCATGATACAAC	55298
rs78756020	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71986790	AAAAAAAAAAAAAAA[A/G]AAAAAAAATACAAAG	55298
rs78764135	snp	A/G	0.078151	0.181571	intron-variant	RNF121	GRCh38.p7	11:71982423	CATGGTGAAGATTTC[A/G]TGTTCGAGATACCAT	55298
rs78880558	snp	A/G	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71951239	GCAATAATGAAAGTC[A/G]TCTAAGCCAACTCTC	55298
rs78891018	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71939536	TCAAGTTAATAGCCA[A/G]CCATTTTCACAGATC	55298
rs78971578	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931581	GGTCTACTGTGTGTT[A/G]TGCACTGATAATTCA	55298
rs79000239	snp	A/C	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71995286	TTGTGAGATAGGGAT[A/C]ATTATCCTTACTTCA	55298
rs79013664	snp	C/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71952590	GAGGCAGGCAGGTCA[C/G]TTGAGGTCAGAAGTT	55298
rs79027059	snp	A/C	0.5	0	missense, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71960788	CCAAGCACCGTGGCC[A/C]TGAAGCTATGCATGC	55298
rs79074375	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71937631	TGAATGCCTCTATTG[C/G]AGTGTCCTTCAGATT	55298
rs79075276	snp	A/G	0.0603597	0.1629	intron-variant	RNF121	GRCh38.p7	11:71995140	GAGGACCCTCTAATG[A/G]GATCCCTCAGTTTAG	55298
rs79155552	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71955087	CAGGGCCAGGACTAG[A/G]GTGAGGGAAACAAGG	55298
rs79171896	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71941951	TTTTTTTTTTTTTTT[A/G]AGACGGAGTCTTGCT	55298
rs79173823	snp	A/G	0.0360663	0.129354	intron-variant	RNF121	GRCh38.p7	11:71975331	CTTTGAGTCTCATCT[A/G]CCTCTTTAGGCTCAT	55298
rs79174393	snp	C/T	0.0460142	0.144533	intron-variant	RNF121	GRCh38.p7	11:71951573	TGAGGCTCTAATGTA[C/T]AATGATCATGCCTGT	55298
rs79204966	snp	A/G	0.093417	0.194889	intron-variant	RNF121	GRCh38.p7	11:71964623	GCTGGGACTACACGC[A/G]CACACCACAGCACCA	55298
rs79234989	snp	C/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71946514	GTTTACAGGCATATG[C/G]TGTCACATTCAGCTG	55298
rs79270850	snp	A/T	0.02016	0.0983543	intron-variant	RNF121	GRCh38.p7	11:71951313	TATTCATTGACATAT[A/T]GCAAGTAAAGACCTG	55298
rs79278569	snp	A/G	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71943102	AGGTTTCAACGTACT[A/G]ATTTTGGGGAACACA	55298
rs79290098	snp	A/C	0	0	intron-variant	RNF121	GRCh38.p7	11:71980267	ACAGAATGGGAACCT[A/C]TAAAGCAAAGTGGTT	55298
rs79316353	snp	A/G	0.0539704	0.155153	intron-variant	RNF121	GRCh38.p7	11:71954424	AGTTCTTGCCCTTCC[A/G]AGCTGCCTTCCCTGA	55298
rs79333927	snp	C/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71940459	TGAATTTCATTAGAG[C/T]ATTAGGAATGAACGC	55298
rs79360732	snp	A/G	0.0607341	0.163335	intron-variant	RNF121	GRCh38.p7	11:71977934	CATAAATGTTGCCAC[A/G]AGATGGCACTAGAGG	55298
rs79366031	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71942853	ATTTCTCACAGTTCT[C/G]GAGGCTGGGAAGTCT	55298
rs79368633	snp	A/G	0.0584853	0.160693	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929940	TTTAAACGATAAATA[A/G]GTGTCTCTCTCTTCT	55298
rs79394464	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929766	CGGGTTCTGGGCCAG[G/T]TGCTAGGGAGACAAG	55298
rs79411337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934015	GTTTCTAATTACTTC[C/T]GGGCTTTGTTGGTGC	55298
rs79450267	snp	G/T	0.0349115	0.127424	intron-variant	RNF121	GRCh38.p7	11:71992245	CTTACAATTTTTACT[G/T]TGTGAACTCTTATTC	55298
rs79487915	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71994610	TAACTCTGGGCCTCC[C/T]GCTGCCACTGTGCCT	55298
rs79488726	snp	A/G	0.0279526	0.114869	intron-variant	RNF121	GRCh38.p7	11:71968575	GTCAGTTCTAGAGAG[A/G]AGAAGCAGAGCATAA	55298
rs79501661	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71966036	TTGATACATTTTTTT[G/T]GAGACAGAGTTTCCC	55298
rs79524029	snp	A/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71943947	GAGACTGGAAAGGGA[A/G]GCAGATGTGATGACA	55298
rs79544481	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71955824	CATGTGTCCCCTCAG[A/G]GTATCTGACCTCTAT	55298
rs79584709	snp	A/G	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71974492	GTAGTCAGGGTAGGT[A/G]TTTATCTTCAGTTTT	55298
rs79662301	snp	A/G	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71978473	CATTAATAAGAAATT[A/G]CTTATAACCTTATCA	55298
rs79664808	snp	C/T	0.0930568	0.194599	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996056	GGAAGTGAGGCTGGG[C/T]CCTTCCAGAAAGCAG	55298
rs79733620	snp	A/G	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71930553	CACTAGAGACTACAG[A/G]TGTTTGGATACCAGT	55298
rs79844647	snp	A/G	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71989468	GGAAAACAGAATTGA[A/G]AATCTTGATCATTTT	55298
rs79867100	snp	A/C	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71992135	CACAAAATGTATAAT[A/C]ATCATGCAAAGGCAC	55298
rs79926580	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71964699	GCCTAGGCTGGTCTC[A/G]CCCTCCTGAACTCAA	55298
rs79932181	snp	A/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71936712	TTCAGGTCACTTTTT[A/T]ATTATGACTTAATAA	55298
rs79965181	snp	C/T	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71944886	CCCTAAATCTTCCTT[C/T]AGTCCTAGCTGTATG	55298
rs80033501	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71960184	AGTCACTGTTGGATT[A/G]GTATAAAGTTGAAGC	55298
rs80038965	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71994390	TGCCTGACACAGCTT[C/T]TGATCACCAGCCCCA	55298
rs80043345	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71993264	ATTTTGAAGTATACA[A/G]TTCATGCATTAATTA	55298
rs80051260	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71959652	CTTTTTTTTTTTTTT[G/T]TGAGATGGAATCTCA	55298
rs80132940	snp	C/T	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71986024	AATTAGGTTGTACAC[C/T]GTCTTCATTGGCTCC	55298
rs80179673	snp	A/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71981437	TTGTTGTTGTTTTTT[A/T]TAAAAATATTCTTTG	55298
rs80213700	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71966880	TTTTTGTTTTTTTTT[G/T]TTGAGACGGAATCTC	55298
rs80221410	snp	A/C	0.0372196	0.131242	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928177	TGGCATGACAGCCTA[A/C]GTAAGACGCGGAATG	55298
rs80330432	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71980982	ACTAGAAGATTTTAA[A/G]CTATGTTTGTGACTT	55298
rs111370075	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71969689	CACCTCAGCCTCCCA[A/G]GTAAATGGGACCACA	55298
rs111421452	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71948463	GAGGTTGCAGTGACC[C/T]GAGATTGCGCCACTG	55298
rs111463214	in-del	-/ACAA/ACAAAA	0.0836354	0.186609	intron-variant	RNF121	GRCh38.p7	11:71942805	GATATATATATGTAC[-/ACAA/ACAAAA]ACACACACACACACA	55298
rs111500493	in-del	-/A	0.469642	0.119404	intron-variant	RNF121	GRCh38.p7	11:71952807	TCTCAAAAAAAAAAA[-/A]TTTCATAAATACAAT	55298
rs111511805	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71984731	CTACAGGTGTGTGCC[A/G]CCACACCCGGCTAAT	55298
rs111576125	snp	C/T	0.106987	0.205054	intron-variant	RNF121	GRCh38.p7	11:71942825	ACACACACACACACA[C/T]ATATATGTATATATT	55298
rs111610022	snp	G/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71944243	GAGACTGAGGCAGGA[G/T]AATCACTTAAAGCTA	55298
rs111650927	snp	A/G	0.5	0	stop-lost, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71995525	CTGCAAAGAGAAGGT[A/G]GACCTCAAGAGGATG	55298
rs111692765	snp	A/T	0.5	0	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927842	AAAAATGATTATTTT[A/T]AAGTAAATGGGATGC	55298
rs111746407	snp	G/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71937390	CGACCTTGGCTCACT[G/T]CAACCTCCGCCTCCT	55298
rs111821738	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71963792	TGGATGGTCGTGGCA[C/T]GTCACGACCTTGTCA	55298
rs111977319	snp	G/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71994958	TGCTGTCCAGACCCT[G/T]GAGTGTAGGAGAGCC	55298
rs111977851	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71968151	ACTGCAACCTCTGCC[C/T]CCGGTTCAAGCGATT	55298
rs111984209	snp	A/G	0.0777841	0.181223	intron-variant	RNF121	GRCh38.p7	11:71961999	TTGAGACAGAGTCTC[A/G]CTGTGTCGCCCAGGC	55298
rs112020702	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71936673	TGCTGAGATTACAGG[C/T]GTGAGCCACTGCGCC	55298
rs112026959	snp	A/C	0.0138799	0.0821421	intron-variant	RNF121	GRCh38.p7	11:71992571	TAAAGTCACAGTTTC[A/C]AAGAAACTGTCAGTG	55298
rs112039868	snp	A/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71977463	AGCTCTCAGTTAAGA[A/G]GCAATCCGTTTAAAT	55298
rs112081883	in-del	-/TGTCTC	0.216649	0.247765	intron-variant	RNF121	GRCh38.p7	11:71993476	CAATATTTGTCCCTT[-/TGTCTC]TGGCTTTTTTCACTT	55298
rs112128033	snp	A/G	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71932328	ATGAAACTGAGGCTA[A/G]AGAGGCTAAAGAACT	55298
rs112143075	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71936443	CACCCAGGCTGGAGC[A/G]CAGTGGCACGATCTC	55298
rs112200962	snp	C/T	0.0217236	0.101931	intron-variant	RNF121	GRCh38.p7	11:71974131	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	55298
rs112275668	snp	C/T	0.031825	0.122064	intron-variant	RNF121	GRCh38.p7	11:71935972	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	55298
rs112335672	snp	G/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71949156	GGCATGGTGGTTCAC[G/T]CCTGTAATCCTAGCA	55298
rs112341121	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71963189	TGATAGTGTCCTTTG[A/G]TGCATAAACAGTTTT	55298
rs112341777	in-del	-/T	0	0	intron-variant	RNF121	GRCh38.p7	11:71978070	AAAAAATTTTTTGTA[-/T]TTTTTTTTTTTTAAG	55298
rs112386846	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71966570	CACTGCAGCCTCAAA[C/T]ACCTGGGCCCAGGCA	55298
rs112447973	snp	C/T	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71950766	CACACCATTCCCCTG[C/T]CTCAGCCTCCCCAGT	55298
rs112501336	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71958398	AAAGAAGAGTCAATA[C/T]GTCCTTTGTTGTTAT	55298
rs112523066	snp	C/G	0.0178098	0.0926698	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997700	GTCTGGGGGTGGTTG[C/G]GCCTGCCTTTCTGCT	55298
rs112582426	snp	A/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71950499	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	55298
rs112587056	snp	A/G	0.0360663	0.129354	intron-variant	RNF121	GRCh38.p7	11:71976442	CTCACGGCAACCTCC[A/G]CCTCCCGGGTTCAAG	55298
rs112717596	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71956126	TATTTCAAATGTTCA[A/G]CTTATGGGACTTTCC	55298
rs112848434	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71939181	AGTGCTGGGATTACA[C/G]GTGTGAGCCACTGTC	55298
rs112904022	in-del	-/AA	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71973187	GTGAAACTCCATCTC[-/AA]AAAAAAAAAAGAGGG	55298
rs112911019	snp	C/T	0.078151	0.181571	intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962255	AGGCGTGAGCCACCG[C/T]GCCCGGCAGATTTTT	55298
rs112913215	in-del	-/AC/ACAC/ACACAC	0.0721257	0.176631	intron-variant	RNF121	GRCh38.p7	11:71950014	CAAAAACAAAACAGA[-/AC/ACAC/ACACAC]ACACACACACACACA	55298
rs112924905	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71975543	GTGCCTCTCCTCTGT[A/G]TTTTCTTGGTCACCA	55298
rs112943353	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71988932	CAGGCTCCTGAAGGG[C/T]TTAGAGGAATTCATC	55298
rs113007057	snp	C/T	0.0777841	0.181223	intron-variant	RNF121	GRCh38.p7	11:71967117	ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA	55298
rs113060936	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71962889	CCGTTTTTTTTTAAA[-/A]TTTTATTTATTATAG	55298
rs113063672	in-del	-/A	0.5	0	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927525	AAAGAAAAAAAAAAA[-/A]GCACTCAGATTAAAA	55298
rs113071721	snp	C/T	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71949157	GCATGGTGGTTCACG[C/T]CTGTAATCCTAGCAC	55298
rs113113024	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71934940	GTGTTCCAAATGCAT[C/T]CTTTTTTTTTTTTTT	55298
rs113137594	in-del	-/A	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71991955	ACAAAAAAATGAGAC[-/A]AAAAAAAAAAAAACC	55298
rs113148584	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71955552	CTGGGTTCTTAAAGG[A/G]TAACTAGGATGTAGA	55298
rs113171794	snp	A/G	0.0494327	0.149241	intron-variant	RNF121	GRCh38.p7	11:71930490	AATTGACAGGTGATC[A/G]CAGCAGGGGGATTTT	55298
rs113214462	snp	A/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71995276	CATAACAGTCTTGTG[A/G]GATAGGGATCATTAT	55298
rs113226088	in-del	-/CAAGCTCT	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71953581	TTTTCTGTTTCTTAA[-/CAAGCTCT]CAGGGTACTCTTGGT	55298
rs113242207	snp	C/G	0.0119091	0.0762411	intron-variant	RNF121	GRCh38.p7	11:71933265	GTGCCTGTGAATCTG[C/G]ATGTGTCCACTCTCA	55298
rs113308094	snp	A/G	0.0930568	0.194599	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926755	AAAATACAAAAATTA[A/G]CTGGGTGTGGTGGCA	55298
rs113447011	snp	A/C	0.077417	0.180873	intron-variant	RNF121	GRCh38.p7	11:71981201	CTACAGGTGCCTGCC[A/C]CCACACCCGGCTAAT	55298
rs113481955	snp	G/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71984815	CATGTTGGCCAGGCT[G/T]ACCTCAAGTGATCTG	55298
rs113534509	snp	A/G	0.0763149	0.179815	intron-variant	RNF121	GRCh38.p7	11:71966301	TGGGATTACAAGTGT[A/G]AGCCGCCGTGCCTGG	55298
rs113537506	snp	C/G	0.0930568	0.194599	intron-variant	RNF121	GRCh38.p7	11:71936424	AGACAGAGTCTCGCT[C/G]TGTCACCCAGGCTGG	55298
rs113610613	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71942048	TGCCATTCTCCTGCC[C/T]CAGCCTCCCGAGTAG	55298
rs113699392	snp	A/G	0.0174175	0.0916809	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996812	AGCACTGAGGCCCCA[A/G]GTGTCCTCCCTCCCC	55298
rs113720707	in-del	-/G	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71988652	CTTAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA	55298
rs113775649	in-del	-/A	0	0	intron-variant	RNF121	GRCh38.p7	11:71945162	TTGGCTAATTTTTAA[-/A]TTTTTTGTAGAGATG	55298
rs113808466	snp	A/T	0.0221141	0.102801	intron-variant	RNF121	GRCh38.p7	11:71947342	AAAATAACAAAAATT[A/T]CCCAGGCATGGTGGC	55298
rs113915506	snp	A/C	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71960969	CTAGGTCCCAGCCTA[A/C]CCCAGGCCACATGGA	55298
rs113931068	snp	C/G	0.5	0	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929058	GAGGGGGCGAGCCGT[C/G]AAGATGGCGGCAGTG	55298
rs113947803	snp	C/T	0.5	0	intron-variant	RNF121	GRCh38.p7	11:71946029	GGTGGGAGTATCACT[C/T]GAGCCCAGGAGGTTG	55298
rs114098317	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71959365	ACCTGGGTTCTACAC[C/T]TTTTGTTATATTTGC	55298
rs114164129	snp	A/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71959619	CTCTCTAATTCCTTC[A/T]CTTCTCTCTCTCTTC	55298
rs114190657	snp	C/T	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71931633	TTACCAATTTACAGT[C/T]GAGTGAAGAGACATG	55298
rs114399122	snp	G/T	0.0322114	0.122752	intron-variant	RNF121	GRCh38.p7	11:71967629	GGTTTCACCATGTTG[G/T]CCAGGATAGTCTCGA	55298
rs114501533	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71991236	AAAAGTTGAAATTAT[A/T]AAAAAAAAAATTAGC	55298
rs114532907	snp	A/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71937606	TTCCATGGTCAGCCT[A/T]TTCCTTCTTTGAATG	55298
rs114716742	snp	A/G	0.0599851	0.162463	intron-variant	RNF121	GRCh38.p7	11:71931081	TCAGGTGAGCCGCCG[A/G]TCTTGTCCTCCCAAA	55298
rs114794510	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71979877	GATTTAATTATTCTC[C/T]GGGCCTACTGTTTTG	55298
rs114823890	snp	A/T	0.0185938	0.0946107	intron-variant	RNF121	GRCh38.p7	11:71952020	ACAAAAATTTAAAGA[A/T]GGATGTTCATAGTAG	55298
rs114884910	snp	C/T	0.00835141	0.0640778	intron-variant	RNF121	GRCh38.p7	11:71982382	CCTATCCTTTGACTG[C/T]TTAAGGGTTTTAAGC	55298
rs114933962	snp	A/T	0.0414363	0.137845	intron-variant	RNF121	GRCh38.p7	11:71975941	ACTTATGTGGTAAGG[A/T]TTACTATGTGTAGGT	55298
rs114937549	snp	C/G	0.0123036	0.0774623	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927689	ATAGGCTTGAGAGTA[C/G]AAAAAACAGGTAAGT	55298
rs114991750	snp	A/C	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71949158	CATGGTGGTTCACGC[A/C]TGTAATCCTAGCACT	55298
rs115021526	snp	A/G	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71942240	GCCCGGCAATGAAAA[A/G]ATTTTGATTGGGTTT	55298
rs115131624	snp	C/T	0.0607341	0.163335	intron-variant	RNF121	GRCh38.p7	11:71946145	AAGAAAAGAAAAATC[C/T]GCACAGAAACTTATA	55298
rs115230148	snp	A/G	0.0189856	0.0955633	intron-variant	RNF121	GRCh38.p7	11:71991299	TTAGGGCCATTATAG[A/G]AAAGAGCCACTTTAT	55298
rs115259529	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984142	AATTGCTACCTCACA[C/T]AGGGTGATAAGATGA	55298
rs115259615	snp	G/T	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71933651	CCACTTCATGTTCCC[G/T]CAGCCCGCTTGTACT	55298
rs115322143	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71979450	TTCTCACACACAGTC[C/T]TTTTCTTTCTCTCGA	55298
rs115364895	snp	A/C	0.0614824	0.164198	intron-variant	RNF121	GRCh38.p7	11:71957895	CTGACCAATGAGGTG[A/C]TATCAACCTTAGAAT	55298
rs115432361	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997161	GTGCCAGCGGTCACT[C/T]TGCCACATCACTTCC	55298
rs115561667	snp	C/T	0.00755907	0.0610114	intron-variant	RNF121	GRCh38.p7	11:71966467	TTTTATTAATAACTT[C/T]TTTAGTTCATTTCTG	55298
rs115566969	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71942787	GTATATATATATATA[G/T]ATAGATATATATATG	55298
rs115637270	snp	C/T	0.00114047	0.0238523	intron-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71978196	GTGAGCCACCATGCC[C/T]GGCCTACAGTAGAAA	55298
rs115658031	snp	C/T	0.0123036	0.0774623	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928909	CCCTGAAACGTGCAG[C/T]AAGTAGATAACCTCC	55298
rs115823809	snp	A/G	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71973874	ATAAATTTAAAAGAA[A/G]AAATATAAAATTTAA	55298
rs115933128	snp	A/G	0.0329836	0.124112	intron-variant	RNF121	GRCh38.p7	11:71946417	ATTTATTTTTGAGAT[A/G]AGGTCTTGCCGTGTT	55298
rs116012482	snp	C/T	0.0667028	0.170006	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997411	TCTGAGAGGGGGCTT[C/T]TAGGAAGGCCCCAGC	55298
rs116046221	snp	A/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71981350	CCACCACGGCCAGCC[A/G]AGTAAATACTTTCTT	55298
rs116050637	snp	C/T	0.030278	0.119257	intron-variant	RNF121	GRCh38.p7	11:71950836	GGTAACTAGGGAAAC[C/T]ATAGCAGTTTTGAAG	55298
rs116203794	snp	A/G	0.00914312	0.0669923	intron-variant	RNF121	GRCh38.p7	11:71942229	TGAACCACCGTGCCC[A/G]GCAATGAAAAGATTT	55298
rs116205525	snp	A/C/G	0.0119091	0.0762411	intron-variant	RNF121	GRCh38.p7	11:71982985	ATGCATGGGAGGAGC[A/C/G]TAGGTTTAGACTGAA	55298
rs116279949	snp	C/T	0.0298908	0.118541	intron-variant	RNF121	GRCh38.p7	11:71979950	CAAAACCTTCCAGCC[C/T]TTCTTTCCATATGCC	55298
rs116376379	snp	A/C	0.0197687	0.0974348	intron-variant	RNF121	GRCh38.p7	11:71950906	ACAGATTTTATTTGA[A/C]TTATTATAGCATTTT	55298
rs116488882	snp	A/G	0.040671	0.13668	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930100	GATGTTGAGTGTGAA[A/G]GGAATGAAGGGACAG	55298
rs116568773	snp	G/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71957529	TTTGAGCAAGTTACT[G/T]AACTTCTCACAACCT	55298
rs116599233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994145	GCGCCCAGCCTCCTC[C/T]TATTTCTTTAAATTC	55298
rs116603454	snp	C/G	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71988799	TGCACTCCAGCTCAG[C/G]TGACAAAGGGAGACC	55298
rs116677569	snp	A/G	0.00716266	0.059414	intron-variant	RNF121	GRCh38.p7	11:71985752	CTCCCATCACAGATA[A/G]AATAGTGGCTCCTGA	55298
rs116765276	snp	A/G	0.0134861	0.0810011	intron-variant	RNF121	GRCh38.p7	11:71944362	ACTTAGGTGAATGAC[A/G]TGGATCAGATGTGCA	55298
rs116945033	snp	A/G	0.0134861	0.0810011	intron-variant	RNF121	GRCh38.p7	11:71941265	AGCAAAGACAGTAGG[A/G]TAGAGAGAAGTGAGC	55298
rs117030212	snp	C/T	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71971629	AACAGGCCAGAGATA[C/T]GAACACATTTACAGG	55298
rs117049677	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71988379	GAGCCCTAAGCCTAC[A/G]ACAGTGCACTGAAGC	55298
rs117176298	snp	A/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71961286	TAAAGAAGGATCGGG[A/T]GTGGTGGCTCATGTT	55298
rs117219949	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71955120	CTAGGGTATAAACTT[C/T]AGAGAGCCATTCACT	55298
rs117281243	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968576	TCAGTTCTAGAGAGG[A/G]GAAGCAGAGCATAAA	55298
rs117394335	snp	C/T	0.0170251	0.090679	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927331	TTAAGGTCAGGAGTT[C/T]GAGACCATGGCCATG	55298
rs117528628	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71940075	GTGGATAGGAGGCCA[A/C]TTTAGGCCAAGGTAA	55298
rs117770479	snp	C/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71968229	CATGCCTAGCTAACT[C/G]TTTGTATTTTAGTAG	55298
rs117876644	snp	A/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71940674	TACTGTGCTGGGGAC[A/G]CAAAGATGAAAATGT	55298
rs117887501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991667	TGAGAACCAGGCAGA[A/G]GAAAGAGCATTCATA	55298
rs117963208	snp	C/T	0.0170251	0.090679	intron-variant	RNF121	GRCh38.p7	11:71982295	GAGCCAGGATCACAC[C/T]GTTACACTCCAACCT	55298
rs117979147	snp	A/G	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71965807	CTATTATAGTTTACA[A/G]TCCATCAACACAGAT	55298
rs118005509	snp	A/G	0.00953873	0.0683987	intron-variant	RNF121	GRCh38.p7	11:71933324	AAATCATGCATATCA[A/G]TGAGGAGTTTCTAAC	55298
rs118006000	snp	A/T	0.00795532	0.062565	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71996975	CATTGAAGATTTGTT[A/T]TGGGACAACTGGAAG	55298
rs118010960	snp	A/G	0.0138799	0.0821421	intron-variant	RNF121	GRCh38.p7	11:71987964	CAGTCCAGATGTGTT[A/G]TACTAATCACAGGTC	55298
rs118045948	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928074	GTATACGTAGGGGTG[A/G]GACAGTGAATGGTGT	55298
rs118134741	snp	A/G	0.000214152	0.0103455	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990671	ATGGAGTTCTGGAAC[A/G]GGACTTTGCAGAAAT	55298
rs137900463	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71957950	ATTTTATTTAGATTA[A/G]AACTATTGACTATAA	55298
rs137968138	in-del	-/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927437	GAGACATGAGAATCG[-/T]TTGAACCCAGTAGGC	55298
rs137970270	in-del	-/TA			upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997227	GTGTGTGTGTGTGTG[-/TA]CGTGAGGCAGAAGAA	55298
rs137972494	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996772	GTATAGAAGAGCTAA[C/T]GTACTCAGGCTTGTG	55298
rs138053782	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987282	CATGATTTGTTCTGG[C/G]AGAAAGCAAGGAATG	55298
rs138093391	snp	C/T	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71943507	TACGCCAGCCTCGTG[C/T]ATGTTGGGAGAATCC	55298
rs138131011	snp	A/G	0.0298908	0.118541	intron-variant	RNF121	GRCh38.p7	11:71947257	TCACACCTGTAATCC[A/G]AGCACTTTGGGAGGC	55298
rs138169295	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71942900	CAGATATGATGTCTG[C/G]CAAAGGCTCTGTGCT	55298
rs138293171	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936945	TGCTTGTAGATGTGG[A/G]TTCTGTTAAGGATAA	55298
rs138320257	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71970318	TAACAGTATTGAACT[A/G]TATACTCAAAGATGA	55298
rs138326131	in-del	-/T			intron-variant	RNF121	GRCh38.p7	11:71938826	TTTGGTTTTGAGCTC[-/T]GTAAATATGGCAGTG	55298
rs138438224	snp	A/G	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71966069	TTGTTGCCCAGGCTG[A/G]AGTGCAATGGCACAA	55298
rs138452805	snp	C/T	3.29761e-05	0.00406041	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982829	GCACTGGTGGAGGTT[C/T]CTAGTGATCTGGATC	55298
rs138460444	snp	A/T	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71968196	TCCCAAGTAGCTGGG[A/T]TTACAGGCTCCTGCC	55298
rs138585980	snp	A/G	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71993495	CTTTTTTCACTTAGC[A/G]TAGTGTTTTCAGAGT	55298
rs138684224	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953002	AAGAAAAAACATATT[C/T]CTCTTGTCTGAGATT	55298
rs138704476	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957447	CTTGAATGTGTAAGC[A/G]GATGATTGCACCAAA	55298
rs138704812	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71948090	TGGAAAGCTGCAGTG[C/G]ATATAGGAAAGAGTG	55298
rs138736756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981827	TCTAGTTTAGAGGAA[A/G]TGGGAATATGGCCCA	55298
rs138742389	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952253	TCCCATTTATATGAA[C/T]TGTCTAGAATAGGCA	55298
rs138925738	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71962398	TCAATCTGGGAAACA[G/T]TTAAGAGGCTGCTCT	55298
rs138928751	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931315	TACTTGTTTCATTTC[C/G]TGAGAAAAGGTATAA	55298
rs138981712	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928504	TAGCACAGGAATGCG[C/T]TCTGGGGCTTCAAGA	55298
rs139071623	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71932530	ATGTAAAAATTGATA[C/G]CGTATATTTGATAAG	55298
rs139108240	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937183	GCACTTACCATGTCG[G/T]ATTGTCTTTTCCATT	55298
rs139112857	snp	C/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71972363	GATTAGCCATTAGAG[C/T]TTTTAAAAAAATGCC	55298
rs139162771	snp	A/C	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71939422	CACCGCCCCCCGCAA[A/C]TTCCCTCCACCCCTA	55298
rs139270352	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71964865	ATGGGATGGTTGACT[A/G]GACTTCTTGAAGTCC	55298
rs139288507	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928790	CTCCAAAGGGAAGAA[C/T]TGGTTAAATAGTTGC	55298
rs139298254	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71983725	TCAAGGAGTACTCTG[G/T]TTAATGGAGGAGATG	55298
rs139351100	snp	C/G	0.0217236	0.101931	intron-variant	RNF121	GRCh38.p7	11:71994122	TGGGGTTACAGGCGT[C/G]AGCCACCGCGCCCAG	55298
rs139370367	snp	A/G	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71950269	ATTTTTGATGTATGC[A/G]TATGGTAGTCCCTTG	55298
rs139443701	snp	A/G	0.0107246	0.0724382	intron-variant	RNF121	GRCh38.p7	11:71987884	AGATGACACAGATGG[A/G]TGTGGAAGCCACCTG	55298
rs139479899	in-del	-/G	0.00795532	0.062565	intron-variant	RNF121	GRCh38.p7	11:71947281	TGGGAGGCCAGCGCC[-/G]GAGGATCACTTGAGC	55298
rs139576826	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959343	AGTGAACACCTTTAT[A/G]CTTACCACCTGGGTT	55298
rs139602688	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933614	AAGGATTTTTCTGTT[A/G]TAGTCCACTGATTGG	55298
rs139684525	snp	A/G	0.00557542	0.0525036	intron-variant	RNF121	GRCh38.p7	11:71959872	AACTCCTGACCTCAC[A/G]TGATCCTCCGGCCTC	55298
rs139685106	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71962799	CACAGAAGCTGCACA[A/G]TTTTCCATTCTGTCC	55298
rs139723729	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71970807	GCAAGAAAGAAAGCA[A/G]CTACCAAGACAGGGA	55298
rs139743297	in-del	-/A			intron-variant	RNF121	GRCh38.p7	11:71971645	AACACATTTACAGGA[-/A]AAGGAAACCCAAAAG	55298
rs139860641	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71966337	TATTTCCATTTTTAT[C/T]GAAGTAATACATACC	55298
rs139872070	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71954692	GCACCTTCATGCCTG[G/T]CCCAGTATTCCAGAT	55298
rs139917427	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943664	CAGATGTAATAATTG[C/T]TATAATATGAAGAAG	55298
rs140013272	snp	A/G	9.8925e-05	0.00703226	missense, nc-transcript-variant	RNF121	GRCh38.p7	11:71990610	AGGATCAAACCAGAA[A/G]ATGCCATGGACTTTG	55298
rs140031620	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71994541	AAGATGAGGTCGATT[G/T]GACTTGTAAAAGATT	55298
rs140148002	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930416	GCCTGGTAGTGGGAT[A/G]AGTTGGAGGAGTTGG	55298
rs140266655	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71942803	ATAGATATATATATG[A/T]ACACACACACACACA	55298
rs140450388	snp	G/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71987270	AGACAGGCTCTCCAT[G/T]ATTTGTTCTGGCAGA	55298
rs140451226	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71985594	CATCACTGCTTGCCT[A/G]GCCACAGCAAGGAGG	55298
rs140469891	in-del	-/AGAC	0.0402882	0.136092	intron-variant	RNF121	GRCh38.p7	11:71971593	CTACAAATCAACAAA[-/AGAC]AGCAACTCCAATAGA	55298
rs140490589	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71951827	CAGAGATTATAAGTA[C/T]TGGGAAGGATATGGA	55298
rs140530953	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955376	GATTCAGTGGGTCTG[C/G]AGTGGTACCTGAGAT	55298
rs140557805	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979321	TGGAACTAGAACTCC[A/G]GTTTACTGGGCTTCT	55298
rs140564269	snp	A/C	0.0107246	0.0724382	intron-variant	RNF121	GRCh38.p7	11:71964142	ATCTTCCAGTACCTG[A/C]ACACAGGATATCTTT	55298
rs140708932	snp	A/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929434	GTAGGACCGAAGGGC[A/T]AAGAGGTAGTTTGAG	55298
rs140741370	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71965754	TGTGTTTTAATTATT[A/G]GTGGAACTTGCCAAA	55298
rs140786053	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71930804	TCATTGAGATAAACA[C/G]CAGAAGTTTTGGCAG	55298
rs140938945	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71990374	GTAGGAGGGGATACT[A/G]TAGCTTGGTCTTCAC	55298
rs140943548	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71946921	CACCCAGGCTGGAGT[A/G]CAGTTGCATGATCTC	55298
rs140974982	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993738	TTGGTCATTTGGTAA[C/T]TTTATGTTTAACTTT	55298
rs140977060	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945146	GTGTGTGCCACCACA[C/G]TTGGCTAATTTTTAA	55298
rs141017071	snp	C/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71992701	CTGAGATTTCTGATT[C/T]GGCAACTGCTTGGAT	55298
rs141151766	snp	A/G	0.00676609	0.0577691	intron-variant	RNF121	GRCh38.p7	11:71987691	AAACCTAAAATATTT[A/G]CCATCTGGCCCTTTA	55298
rs141161587	snp	A/G/T	0.000139782	0.00835891	intron-variant	RNF121	GRCh38.p7	11:71995570	TCCTTTATTGGGGTC[A/G/T]TTGTTGGGAGTGGGC	55298
rs141163143	snp	A/G	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71947454	TGATCAAGCCACTGC[A/G]CTACAACCTGAGTGA	55298
rs141194893	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71991631	TGACTTGAACAATGA[A/G]TAGCAGTTAAGTGGA	55298
rs141224189	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943866	AATGCCACCTTCAGG[C/G]AACTGTATGCAGTTT	55298
rs141275423	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71961133	ATAGGTTTTCCCTTC[A/G]AAACATTGTGGGACA	55298
rs141356177	in-del	-/ACAC/ACACAA/ACACAAAC/GTACACAA	0.483563	0.0891524	intron-variant	RNF121	GRCh38.p7	11:71942803	TAGATATATATATGT[lengthTooLong]ACACACACACACACA	55298
rs141383612	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938053	AAGAGGAAGCAGAGA[A/G]CACAATCCCTGCCAA	55298
rs141400626	in-del	-/ATA			intron-variant	RNF121	GRCh38.p7	11:71976340	CCCTCCATTCTGGGT[-/ATA]TTCTTTTTTTTTTTT	55298
rs141489303	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71968767	TGGAGAAACAACTTT[A/G]AAAAACAGTTTCAAA	55298
rs141501635	snp	C/T	1.6492e-05	0.00287154	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960819	TGAAATGGTCCTCAT[C/T]CTCATCGCAACCTTG	55298
rs141509647	snp	C/G/T	0.000571374	0.0168926	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928625	TTCACTCACTACAAC[C/G/T]CTTTCGTGGAGGGAG	55298
rs141575677	snp	C/G	0.0596104	0.162024	intron-variant	RNF121	GRCh38.p7	11:71993873	TGAGATGGAGTCTCG[C/G]TCTGTTGCCCAGGCT	55298
rs141698424	snp	A/G	0.0588605	0.161139	intron-variant	RNF121	GRCh38.p7	11:71942679	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	55298
rs141734424	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71946397	CTCAATGAATGAATT[C/T]ATTTATTTATTTTTG	55298
rs141753175	snp	A/G	0.00124479	0.0249168	intron-variant	RNF121	GRCh38.p7	11:71982960	GGTTTTCCGAAGCTA[A/G]TGGGTTGGAATGCAT	55298
rs141806411	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71975971	TGTGATAGGAGGGAA[A/G]CAACTCCAACCGTGT	55298
rs141925538	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997825	CTTCAGACTGAGGTT[A/G]CTCTATGTTCTCACT	55298
rs142067692	snp	A/G	0.000287701	0.0119903	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929061	GGGGCGAGCCGTGAA[A/G]ATGGCGGCAGTGGTG	55298
rs142113834	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71958880	TCTGGTCTTTTCTAG[A/C]TCATTCTTTGACTTC	55298
rs142149908	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930068	GTGGTCCTTGAAGGA[A/G]TCACTAGGAGGAAGG	55298
rs142152461	snp	A/T	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71962473	TCTGAAATCTCTAGG[A/T]CTCATCATAGCACTG	55298
rs142186579	snp	C/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71960554	GGTTGCTGGGGGGTC[C/T]GTAGAGCCTGTATTC	55298
rs142256289	snp	G/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71963745	TAGCCAGTTGTCCCA[G/T]CATCATTTATTGAAG	55298
rs142309121	in-del	-/AGA/TAA/TAAG	0.148996	0.228688	intron-variant	RNF121	GRCh38.p7	11:71936407	CACTTTTTTATTTTT[-/AGA/TAA/TAAG]TAGACAGAGTCTCGC	55298
rs142340886	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951322	ACATATAGCAAGTAA[A/C]GACCTGTGCCAGATT	55298
rs142356308	in-del	-/CA	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71979439	TCTCTCTTTTTTTCT[-/CA]CACACAGTCTTTTTC	55298
rs142437922	in-del	-/GGTAGGACT	0.0581099	0.160244	intron-variant	RNF121	GRCh38.p7	11:71957380	CAGTGGCTCATGACC[-/GGTAGGACT]GGTCTTTTGGGATCT	55298
rs142471229	snp	C/T	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71978766	CTTAACTCATTTAAC[C/T]CATACAACCTTCTGA	55298
rs142482538	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981525	TTATACCTGCTACTC[A/T]CTGGAGAAGGATGAC	55298
rs142490094	snp	A/G	0.00835141	0.0640778	intron-variant	RNF121	GRCh38.p7	11:71984316	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	55298
rs142516903	snp	A/G	0.0209421	0.100162	intron-variant	RNF121	GRCh38.p7	11:71984839	TGATCTGCCCGCCTC[A/G]GGCTCCCAAAGTGCT	55298
rs142520917	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71937098	TTTAAATTAATGCCA[A/G]ATTGTTCCTTATCAG	55298
rs142528431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987287	TTTGTTCTGGCAGAA[A/G]GCAAGGAATGTCTGA	55298
rs142530124	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939857	TGGACAAAGAGACTA[C/T]CTCTGCTCTAAAGAA	55298
rs142553959	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71941714	GCAATTTCGAGATTT[A/G]GAAGCAGATATGTTC	55298
rs142570212	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943524	TGTTGGGAGAATCCT[C/G]TTCACTTGTTTATTG	55298
rs142590831	snp	A/G	0.000115318	0.00759249	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994733	GTTCTACAGCGAGTC[A/G]GGCATGCCTACCAAA	55298
rs142682576	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71953497	CAAACTTTAATGTAC[A/G]TATGAATTATTTCAG	55298
rs142703953	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71957465	TGATTGCACCAAATC[A/G]TCTATCTGGGTTTCA	55298
rs142784216	in-del	-/G			intron-variant	RNF121	GRCh38.p7	11:71988532	ATCCTGGCCAGGTGT[-/G]GTGGCTCTCACTTGT	55298
rs142845451	snp	A/G	1.67758e-05	0.00289614	synonymous-codon, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71982901	CCGAAAACCTCTAGT[A/G]CAGACAACCCCAAGG	55298
rs142867071	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71991202	ACAAACCTGCACATG[C/T]ACCCTCTGAATCTAA	55298
rs142889212	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962942	CATTGTGGTGTTGAT[G/T]TGTATTTCCCTAATG	55298
rs142924670	snp	G/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71954246	AGTTTACTCCTTCCC[G/T]TATTTTTTTTTACTT	55298
rs142971367	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933236	ATAGGGCCAGCCAGG[A/G]CATTGCCTGGCTAGT	55298
rs142992592	snp	A/C	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71940949	ATGAAAAGATATGCA[A/C]GGCTTGGAGACGTTA	55298
rs143005474	snp	A/G	0.0422008	0.138995	intron-variant	RNF121	GRCh38.p7	11:71965520	CAAAGTGCTGGGATT[A/G]TAGGAGTGAGCCACC	55298
rs143012903	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71937248	CATTTTTTCATCTCT[A/G]TATTTTCAGCACCTA	55298
rs143110208	snp	A/C	0.0119091	0.0762411	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927880	TGATGTAGATAATTC[A/C]CTGTAATTTTCTGTT	55298
rs143169397	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940561	AAAAGGTAGGTTGGG[A/G]CCAACATGAGGTTGA	55298
rs143180387	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71995733	CAGTTTCCCTATTCT[A/G]GGATTATTGCCTATT	55298
rs143193541	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71982287	GCTACAGTGAGCCAG[A/G]ATCACACCGTTACAC	55298
rs143318416	snp	G/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71968577	CAGTTCTAGAGAGGA[G/T]AAGCAGAGCATAAAT	55298
rs143340960	in-del	-/T	0.0337553	0.125452	intron-variant	RNF121	GRCh38.p7	11:71992467	AGGTTTAGTGATGTC[-/T]TTGTGACAGAAATAT	55298
rs143381266	snp	C/T	0.0016636	0.0287929	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960753	TTTGGCTTTCAGGGT[C/T]GAGCACGCACGCATG	55298
rs143384859	snp	C/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71993625	CTTGAGTTGTTTCCA[C/G]TTTTTGGCTACTGTG	55298
rs143533411	in-del	-/C			intron-variant	RNF121	GRCh38.p7	11:71936905	ACATAGCCCATATCC[-/C]ATATATTTATTGAGT	55298
rs143542435	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71995016	CCCACAGATCAGAGC[C/T]ACTCTTAGGTAAACA	55298
rs143615453	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71943348	AGGCAGTTGGAAATA[C/T]GAGCTTATAGCTCAG	55298
rs143725515	snp	G/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71946654	AGCATGAGGTTTTTT[G/T]TTTTTTTTTAGAGTG	55298
rs143729507	snp	C/T	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71954727	CTAGTTTCCCCCTCA[C/T]TGGATTTGGTTTCTT	55298
rs143741564	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932107	CTCTAGAAGTTGAGA[C/T]GTAATTTAGGCTTTC	55298
rs143804002	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970371	TTTTGAAACCACAAA[A/T]GTAGTTTTGGTTGAC	55298
rs143842636	snp	A/G	0.0482946	0.147699	intron-variant	RNF121	GRCh38.p7	11:71974069	GCCTCAGCCTCCTGA[A/G]TAGCTGGGACTACAG	55298
rs143936937	snp	A/C	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71932294	ATGTGAATTAGATGG[A/C]GTTAACCCCATTTTA	55298
rs143958999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987417	GCTATCCATAATTCT[A/G]TCACCTTAACAGAGC	55298
rs143965563	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972624	CCTGTATATTATAGG[A/T]TGTTTAATAGCATCC	55298
rs144040662	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930422	TAGTGGGATGAGTTG[A/G]AGGAGTTGGATTACC	55298
rs144041745	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71977275	TCCTGAAAGTCAAAA[A/G]TGCCAAGCACCTGTG	55298
rs144063259	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935099	GGTGTGCACCACCAT[A/G]CCTGGCTAATTTTTG	55298
rs144242447	in-del	-/CTC	0.0345262	0.126772	intron-variant	RNF121	GRCh38.p7	11:71956811	CTGGATAATTCACAT[-/CTC]CTCCATAAAGCCTTC	55298
rs144274883	snp	A/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71962974	CTAATGATGTTGGGC[A/T]TCTTTTCCTGTGCTT	55298
rs144287522	snp	A/G	3.29723e-05	0.00406018	utr-variant-3-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996242	TGCTGGACTGGCTTC[A/G]ATACTTGGTAGCCTG	55298
rs144290848	snp	A/G	0.0607341	0.163335	intron-variant	RNF121	GRCh38.p7	11:71959797	TGCACCACCACACCC[A/G]GCTAATTTTTGTATT	55298
rs144380407	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71958699	TGACAGAGCGAGACT[C/G]TCTCCAAAAAAATAA	55298
rs144487188	snp	A/T	0.0130921	0.0798413	intron-variant	RNF121	GRCh38.p7	11:71993533	TGTATAGAATGTATC[A/T]TTCCTTTATATGGCT	55298
rs144506010	snp	A/G	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71949005	GCATTTTGTGTATAT[A/G]TCAAAGGTTATCCTT	55298
rs144512785	snp	A/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71964287	TGTTAATGGAATTTT[A/T]AAAAATTTCCTTTTT	55298
rs144573395	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934703	TTAGGCATGTAAAAT[A/G]AGTGGTGGCAAGTGT	55298
rs144623767	in-del	-/AG/GA	0.305685	0.24372	intron-variant	RNF121	GRCh38.p7	11:71942787	TATATATATATATAT[-/AG/GA]ATAGATATATATATG	55298
rs144703214	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71966327	CCTGGCCTGATATTT[C/G]CATTTTTATCGAAGT	55298
rs144745774	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71985014	GCAGCCTCATCCTCC[C/T]AGGCTCAACCAATTT	55298
rs144782808	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990421	TAGCCTCCTCAAGAG[A/G]TGTTCATGGGCCATA	55298
rs144844588	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984654	CTGGAGTGCAGTTCA[C/T]TGCAACCTCTGCCTC	55298
rs144909661	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952104	GAATGGATAAATAAC[A/G]TGGTATTTATACGAT	55298
rs144961061	snp	A/G	0.0360663	0.129354	intron-variant	RNF121	GRCh38.p7	11:71949495	CCAGGCAGGCAGATC[A/G]CTTGAGGTCAGGAGT	55298
rs145066347	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960215	AGTCCAGACTTTTTA[A/G]GCTTTAACTAGTCTT	55298
rs145158077	snp	C/T	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928012	AGCTGGGGCTACAGG[C/T]TTGCAAGGTATCGAG	55298
rs145178745	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968832	TTTAATTCCTAGATA[C/G/T]ATGCCAAGAGAAGAT	55298
rs145201424	snp	A/G	0.00874735	0.0655527	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926796	ATCCCAGCTACTGAG[A/G]AGGCTGAGGCAGGAG	55298
rs145317204	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929554	AGACCGGGAAAGAGT[A/G]CTAATCCACTAGTAG	55298
rs145413803	snp	G/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71944937	ATTTACTGCTGGCTA[G/T]TAAAGATCAAGTAGG	55298
rs145482978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940652	TTGAGTTCTGATATA[C/T]GCTAGATACTGTGCT	55298
rs145545817	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987271	GACAGGCTCTCCATG[A/G]TTTGTTCTGGCAGAA	55298
rs145582874	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71991980	AAAACCTAGCCGGGC[A/G]TGGTGGCACATGCCT	55298
rs145657041	snp	C/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71984833	CTCAAGTGATCTGCC[C/T]GCCTCGGGCTCCCAA	55298
rs145663728	in-del	-/TAT			intron-variant	RNF121	GRCh38.p7	11:71967821	GTTTACATTATTAAG[-/TAT]TATATGTAAGTATTA	55298
rs145697828	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71988412	GAGATCTAGGATTCA[A/C]ATTTAAGATAATGAA	55298
rs145763693	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990443	TGGGCCATATAAAAA[C/T]AGACAGCAGACTGGA	55298
rs145831280	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71973166	ACTCCAGCCTAGGCA[A/G]CAAGAGTGAAACTCC	55298
rs145885358	snp	C/G	0.0360663	0.129354	intron-variant	RNF121	GRCh38.p7	11:71966064	CCCTCTTGTTGCCCA[C/G]GCTGGAGTGCAATGG	55298
rs145905461	snp	G/T	0.000159987	0.00894247	utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929096	TGGAGGTTGGAGGTG[G/T]TGCTGCTGGGGAACG	55298
rs145907141	snp	A/G	0.0399052	0.1355	intron-variant	RNF121	GRCh38.p7	11:71968163	GCCCCCGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	55298
rs145914063	snp	C/T	0.000400541	0.014146	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960759	TTTCAGGGTCGAGCA[C/T]GCACGCATGCATGCC	55298
rs145985196	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71943608	CAAAGACATAGGCCT[A/T]GCTCTCAGGTTGCTC	55298
rs146102089	snp	C/G	1.64773e-05	0.00287026	missense, nc-transcript-variant, intron-variant	RNF121	GRCh38.p7	11:71987109	TCTTAACTTATTATT[C/G]AAGTGAGTACCCTTT	55298
rs146216796	snp	C/T	0.0178098	0.0926698	intron-variant	RNF121	GRCh38.p7	11:71976600	CTTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC	55298
rs146242450	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71967349	ATGTGGGTTTTTTTT[G/T]TTTTTTTTTTTTTTT	55298
rs146257271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983241	GATCTCTAAATTAGA[C/T]TTTCCATTATATTCT	55298
rs146272073	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975324	CAGCCTCCTTTGAGT[A/C]TCATCTACCTCTTTA	55298
rs146336959	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71959141	CTGAATCTAAGTTTC[A/G]AACTCCCAATCCTAT	55298
rs146378898	snp	A/G	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71962597	TTACTTGTTACTACC[A/G]CATCCTGTAAACATA	55298
rs146436579	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71930697	GAAAGGGTAAATACT[A/G]TATTGAAGTTCTTAT	55298
rs146437212	snp	C/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71977456	TGGTTCCAGCTCTCA[C/G]TTAAGAGGCAATCCG	55298
rs146447899	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71935375	GGTAAGTGACAGAAC[C/T]GGGGTTCAAATCCAA	55298
rs146517579	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71995171	CATCATCCTCTGTTC[G/T]GAATAACACTTGTAA	55298
rs146526952	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981639	AGTTAGAATTGTTTT[A/G]TGCCTTTAAAAAACT	55298
rs146554696	snp	C/T	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71980449	CCTCCCGGATTCAAG[C/T]GATTCTCCTGCCTCA	55298
rs146600939	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71937182	AGCACTTACCATGTC[A/G]TATTGTCTTTTCCAT	55298
rs146637376	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972711	GTCTCCAGACTGCCA[A/G]ATGTCCCCTGGGAAA	55298
rs146676136	snp	C/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71967753	CTGCTATACCTATAC[C/G]CGTTACATACTACAA	55298
rs146687075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71971716	TTAGAGAAATGCACA[C/T]AAAAATATGAGATAT	55298
rs146689179	snp	A/G	0.0205511	0.0992634	intron-variant	RNF121	GRCh38.p7	11:71942010	CGATCTTGGCTCGCT[A/G]CAAGCTCCGCCTCCT	55298
rs146757552	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956011	GCTGGAAAGGCCACC[C/T]TCAATAGTGATGGGC	55298
rs146799185	snp	G/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71951534	GGGTGGCTGGGGTGG[G/T]AGGATTGCTTGAGCC	55298
rs146808946	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71955110	AAACAAGGTGCTAGG[A/G]TATAAACTTTAGAGA	55298
rs146846008	in-del	-/CCCCCCC			intron-variant	RNF121	GRCh38.p7	11:71990886	GTTTGGAAAGCAACA[-/CCCCCCC]CAGCCATAAAAAAAG	55298
rs146918368	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957912	ATCAACCTTAGAATT[G/T]AATAGTGAGAAAAAA	55298
rs146954161	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961266	TACACTAATCTAAAT[C/T]TTTTTAAAGAAGGAT	55298
rs147067176	snp	A/G	0.00795532	0.062565	intron-variant	RNF121	GRCh38.p7	11:71973388	CCCAGCTACTTAGGA[A/G]GTTGAGATGGGAGGA	55298
rs147077630	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71979492	ATAGCTTTACGTACT[G/T]GATGTATATCTCTAG	55298
rs147153171	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71949174	TGTAATCCTAGCACT[C/T]TGGCAGGCTGGGGTG	55298
rs147162344	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71952902	TTTTTTGTGGTGACT[A/G]CATTTGAAAATTCAC	55298
rs147232257	snp	C/T	0.0270983	0.113203	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929024	AGCGGAAGCAGCTGG[C/T]TCGCGCGGGGACTGC	55298
rs147318628	snp	A/G	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71988823	GGAGACCCCCATCTC[A/G]AAAAAAATAAAAATA	55298
rs147328424	snp	A/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71993645	TGGCTACTGTGAGTA[A/T]CGCTGTGAGCACTGG	55298
rs147424648	snp	C/G	0.0170251	0.090679	intron-variant	RNF121	GRCh38.p7	11:71966541	GGCTGGAGGGCAGCA[C/G]CTCCATCATAGCTCA	55298
rs147435279	snp	A/G	0.00953873	0.0683987	intron-variant	RNF121	GRCh38.p7	11:71970700	CTTTAAAAAATTAAA[A/G]GTGGTCCATGCATGG	55298
rs147530840	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71950168	CTCAGCCAAAGAGGT[A/G]AAGGATTGGGTTTCA	55298
rs147540595	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953883	ACCTAAAAAAAATGT[A/G]GCAGTCAACTTCTCA	55298
rs147613491	snp	C/T	0.000214138	0.0103452	intron-variant, synonymous-codon, nc-transcript-variant	RNF121	GRCh38.p7	11:71994836	GAGAACACGTATAGG[C/T]TGTCCTGCAATCATG	55298
rs147662736	in-del	-/TT			intron-variant	RNF121	GRCh38.p7	11:71934942	GTTCCAAATGCATTC[-/TT]TTTTTTTTTTTTTTT	55298
rs147729700	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71984834	TCAAGTGATCTGCCC[A/G]CCTCGGGCTCCCAAA	55298
rs147798294	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960984	ACCCAGGCCACATGG[A/T]GGTGGAGAAAGACAA	55298
rs147834120	snp	C/T	0.00835141	0.0640778	intron-variant	RNF121	GRCh38.p7	11:71964631	TACACGCGCACACCA[C/T]AGCACCAGGCTAATT	55298
rs147904874	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942591	AACATGGTGAAACCC[C/T]GTTTCTACTAAAAAT	55298
rs147989622	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71961764	CGATATGCTGTCTAT[A/G]GTAAATTCACTTTAG	55298
rs147997368	snp	A/T			intron-variant	RNF121	GRCh38.p7	11:71949043	TATTTTATATTTAAT[A/T]GTCTGTCTCTCCCTA	55298
rs148086169	snp	C/T	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71937636	GCCTCTATTGGAGTG[C/T]CCTTCAGATTGGATT	55298
rs148113684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71932172	AAGAGGGTTTAGGAA[A/G]AGAGCTACCAGTAGA	55298
rs148208807	snp	A/C	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71987492	TGCATGAATGGCCTT[A/C]CGTTCAACTAGGCCA	55298
rs148297786	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975910	CTAGCAAATATATTC[A/G]TATTGGAGTGGCCTG	55298
rs148350608	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71968697	AGTCAGTAGATATTC[A/G]TTGATCCTTTCTAGT	55298
rs148377190	snp	C/T	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71965544	AGCCACCACGCCTGG[C/T]CTGCATAGTATTTTG	55298
rs148399749	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71940656	GTTCTGATATATGCT[A/G]GATACTGTGCTGGGG	55298
rs148565044	snp	G/T	0.00835141	0.0640778	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997765	GTGGTGGAATGCCAG[G/T]CTCCTGTCCTGTGGC	55298
rs148573740	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984693	AGGCGATTCTCCTGG[C/G]TTAGCCTCCCAAGTA	55298
rs148574980	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71954156	GAGTTAATGCTTGGC[C/T]CCAAATGAATAAACT	55298
rs148607097	snp	A/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71978014	TGAAGTTTAAACATA[A/T]TTACCAAGCAAAATG	55298
rs148670593	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929979	TATGAGTTCCTTGAA[A/G]GTGAGCTCCTTGAGA	55298
rs148723803	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71963159	CACATTTTATCGGTT[A/G]TCTTGACACTTTATT	55298
rs148777955	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958721	AAAAAATAATATATG[C/T]ATATGTACCTACAAT	55298
rs148915766	snp	C/T	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71956461	ACAGGGAATGAACCA[C/T]CCTAAAATATCAGTA	55298
rs148968024	snp	C/T	0.00244305	0.0348648	intron-variant	RNF121	GRCh38.p7	11:71990729	AGGGGTAAGTTCATC[C/T]GGGTTCTTAAATACT	55298
rs148985005	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71931656	GAGACATGCAAATAG[C/T]GTATTATAATACTAG	55298
rs149037029	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964995	ATGAGGTTTTCATTC[C/T]GCAAAAGTTATGTTT	55298
rs149284177	in-del	-/ACCAGCAGCCAGT	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71980227	CTTCAAGGCTCATGG[-/ACCAGCAGCCAGT]ACCCTCGGGTACACA	55298
rs149336214	in-del	-/A	0.0126979	0.078662	intron-variant	RNF121	GRCh38.p7	11:71995814	AGGCTGTGTTATCTT[-/A]ACACTGGCAGTTCCT	55298
rs149343344	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71981896	GAATTCAAGCCCAGC[C/T]GCATACTCTAGATAA	55298
rs149351812	snp	A/G	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71966306	TTACAAGTGTGAGCC[A/G]CCGTGCCTGGCCTGA	55298
rs149440923	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997603	GAAAGCTGAACATTT[A/G]TCTTGCTTTCTTCTT	55298
rs149495333	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71952866	AGCTAGTAACTTATC[A/G]ATCACCTCAAATACT	55298
rs149557083	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71943153	GATAGCAGAGACGAT[A/G]GAGAAAAGTGGATAA	55298
rs149564923	snp	C/G/T	0.00279162	0.0372561	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928966	TGATGCCCCGCCCCC[C/G/T]CTGCTGGAGTCCGAG	55298
rs149650405	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958079	AAAATATTCTGAATA[A/G]TTTAAAAGATGTTCG	55298
rs149690508	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71967624	TACGTGGTTTCACCA[C/T]GTTGGCCAGGATAGT	55298
rs149869687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944736	AGTGACTCGAGAAGT[A/G]CATGAGGTTGAAGGA	55298
rs149911448	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964769	CAGGCGTGAGCCACC[A/G]TGCCTGGTATTATAA	55298
rs149965526	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959960	TTTCTCATTCCTCTC[C/T]TTTGGATGACTGTGA	55298
rs150017652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994292	CACCAAACCAACATG[A/G]CACTTAATATTTCAC	55298
rs150027243	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71950445	AAAAATTAGCCAGGC[A/G]TGATGGCTTGCACCT	55298
rs150128016	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993076	TTCTCTACTGGATCA[A/G]ATTGAAAACAGTACA	55298
rs150182334	snp	A/G	0.039522	0.134904	intron-variant	RNF121	GRCh38.p7	11:71947017	GGATTACAGGCATGC[A/G]CCACCACACCTGGCT	55298
rs150268132	snp	A/G	0.0592355	0.161582	intron-variant	RNF121	GRCh38.p7	11:71973090	ACTCGGAAGGCTGAG[A/G]CAGGAGAATCGCTTG	55298
rs150276663	snp	C/T	0.0418186	0.138422	intron-variant, nc-transcript-variant, utr-variant-5-prime	RNF121	GRCh38.p7	11:71962253	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCAGATTT	55298
rs150328027	snp	A/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996103	CTGTGGAGCAGCTGG[A/G]AAGTGGGGCAGACCC	55298
rs150338201	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71952493	TTGTGTAAGTTTGTG[A/G]GATACAGACTGATGT	55298
rs150391040	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986034	TACACTGTCTTCATT[C/G]GCTCCTGGGGCACAC	55298
rs150457391	snp	C/T	0.000230859	0.0107413	synonymous-codon, nc-transcript-variant, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71960825	GGTCCTCATCCTCAT[C/T]GCAACCTTGGTGGTG	55298
rs150481339	snp	A/G	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71936872	TGTACATTCCTCAGT[A/G]CCTTGCTCAGTGCTT	55298
rs150583480	snp	A/G	0.0119091	0.0762411	intron-variant	RNF121	GRCh38.p7	11:71976193	TTTATTATAATCCTA[A/G]CTGCTCTCTTATGGC	55298
rs150645774	snp	G/T	0.0919752	0.193722	intron-variant	RNF121	GRCh38.p7	11:71966298	TGCTGGGATTACAAG[G/T]GTGAGCCGCCGTGCC	55298
rs150661655	in-del	-/TGA	0.0599851	0.162463	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71928033	GGTATCGAGTTCACC[-/TGA]GGCTGCTGAAAAATC	55298
rs150678996	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71954332	ATATTAAAGCCAGAT[C/T]ATGTCTTACTCTTAA	55298
rs150731016	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987866	CTTAGGTGTGAGGGA[A/T]TGAGATGACACAGAT	55298
rs150769926	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71942802	TATAGATATATATAT[A/G]TACACACACACACAC	55298
rs150794260	snp	A/C	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71939063	GCACCCGCCATCATG[A/C]CCGGCTAATTGTTGT	55298
rs150846468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970037	GTATTTATCATGTTA[C/T]TAAATAATTAATGTA	55298
rs150856765	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF121, LOC100133315	GRCh38.p7	11:71928706	CCTAGTCCCCACGTC[G/T]CGCTCCTTGGAGCCC	55298
rs150993626	snp	A/T	0.0103295	0.0711199	intron-variant	RNF121	GRCh38.p7	11:71956915	TTTATTATATAATAG[A/T]TAAATTTTCTGTTTA	55298
rs151013070	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963979	ATTATTTTTCAAGAT[G/T]GTTTCAGCTATTCTG	55298
rs151046245	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991329	TCCAGCAGGAAGTTA[A/G]CATTCATTCAGTAGA	55298
rs151047536	snp	A/C	0.0123036	0.0774623	intron-variant	RNF121	GRCh38.p7	11:71959851	ATGTTGGCCAGGCTC[A/C]TCGTTAACTCCTGAC	55298
rs151056056	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71946774	CTGGAGTGCAGTGGT[A/G]CAGTCTCAGCTCACT	55298
rs151110092	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71941031	AGGTTAAACGTAAGG[A/G]GATAGCAGTGAGTGA	55298
rs151318010	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978949	CATTTCATTTTGTTC[A/G]TTCTTTAATGATTCC	55298
rs180712430	snp	C/T	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71937930	TCAGAGAAAAATCTG[C/T]AGGTAAAATAAACTC	55298
rs180980375	snp	A/G	0.00201151	0.0316498	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996354	CCCACCCCACACGCC[A/G]TGGACCTCAGGGCAC	55298
rs180992563	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71976222	GCCTGCTGTCTTATG[A/G]CCATGCTTATTTGTT	55298
rs180995046	snp	C/T	0.000592944	0.0172081	intron-variant, synonymous-codon, utr-variant-5-prime, missense	RNF121	GRCh38.p7	11:71957244	TGATATGTCAGATCT[C/T]TCTCCAGAAGAGCAA	55298
rs181124629	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996668	CTTCTCATCTCTGGC[C/T]GAGAACACTGCTGGG	55298
rs181166384	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71984483	AGACAGGGTTTCCCC[A/G]TGTTAGCCAGGATGT	55298
rs181183004	snp	C/T	0.0611083	0.163768	intron-variant	RNF121	GRCh38.p7	11:71966887	TTTTTTTTTTTGAGA[C/T]GGAATCTCACTCTGT	55298
rs181188756	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948643	CAACATCTACTTTCA[C/T]TTCACTGCCCAAAGT	55298
rs181234552	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71977078	CTACCTCCAGTTGAC[A/T]GCAGTCTATTTCTCA	55298
rs181250634	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71938538	TGGTCAGGCTGGTCT[C/G]GAACTCCCGATCTCA	55298
rs181266970	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71957737	ATGGGGAGCTCTGGT[C/T]AAGAAAATGGGAGAT	55298
rs181284938	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71961390	ACATGGCAAAACCCT[A/G]TATCTACAAAAAATA	55298
rs181341185	snp	A/G	0.0023933	0.0345097	intron-variant	RNF121	GRCh38.p7	11:71992008	CCTGTAGTCCCAGCT[A/G]CTTTGGAGACCAAGG	55298
rs181342819	snp	A/G	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71972753	CTGATGAGAAACACT[A/G]TCCTAGGCTCTAGGA	55298
rs181355332	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953022	TGTCTGAGATTTTGT[A/G]CAGAATAGTACATTT	55298
rs181516450	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71951782	AAAACCACATTGAGA[A/C/T]ACCATTTCATAGTCA	55298
rs181641739	snp	A/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71962295	TCTGAAGAAAGTGAG[A/T]ATGCATATATGCACT	55298
rs181645484	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71990331	CAGTTAGGGGAGGCA[A/C]GGACTAAGAGCAGAG	55298
rs181652820	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71942763	TCCAAAAAAAAAATC[C/T]ATATATCTGTATATA	55298
rs181658883	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972150	TGTAACACAATGCCA[A/G]TTAATAAAAATACAA	55298
rs181662719	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71930900	TGCAGTATTGCAATC[C/T]CAGCTCACCACAACC	55298
rs181848936	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71981617	TGACTTCAAATTTCT[G/T]TCTTAGAGTTAGAAT	55298
rs181918476	snp	C/G	0.00215387	0.0327459	intron-variant	RNF121	GRCh38.p7	11:71960937	TGTCAGTCATCAAGA[C/G]ACCCTTCCTAAGTAT	55298
rs181922554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940744	ACCAGACATGGGAAC[A/G]GATGGTTGTAGTATA	55298
rs181944585	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71936994	TGCAAAGGTTGACTG[A/G]CATGCCTACTATCTG	55298
rs181955031	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71984950	AAATAGAGATGAGGT[C/T]GCACTCTGTCGCCCA	55298
rs181956623	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71967210	TGTTTATACTGATAT[A/G]AATTTCTACTTTATT	55298
rs182069451	snp	C/G	0.00636936	0.0560724	intron-variant	RNF121	GRCh38.p7	11:71972568	AACAGAGGAACTGTT[C/G]GCATTTTGGGCCATA	55298
rs182088922	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71931820	AGAGCAGTGGTTTAC[A/G]TGTGGCATTAATATT	55298
rs182136283	snp	A/G	0.00159808	0.0282221	intron-variant	RNF121	GRCh38.p7	11:71994622	TCCCGCTGCCACTGT[A/G]CCTCTTCTCTAGAAG	55298
rs182140954	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927603	GCTACATATAATTAT[G/T]AAAAATGGACTGGGA	55298
rs182151618	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71956331	TGGGTATGCTTCTGT[A/G]TGACTGCAAGGAGGT	55298
rs182284448	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71959374	CTACACTTTTTGTTA[C/T]ATTTGCTTTATTGTT	55298
rs182289314	snp	C/T	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71939407	GGCTTTTTGGATTTG[C/T]ACCGCCCCCCGCAAC	55298
rs182344487	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997476	CAAACATGGGCCTTC[A/G]GCATTGGGTTTCTAG	55298
rs182354644	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71979151	GTGAGTGGGTGAACA[C/T]TGCCTCTACTCTCCT	55298
rs182359067	snp	G/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71991707	TCACGGGAGAAAGTG[G/T]GGGTGTTTTTGAGGA	55298
rs182365735	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952782	CACTGCACTCTAGCT[A/G]GGGCGATAGAGCAAG	55298
rs182400336	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948983	CTTTTTCTCTGGGGC[C/T]TACACAGCATTTTGT	55298
rs182412447	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71975343	TCTACCTCTTTAGGC[C/T]CATTTCTCACACCTT	55298
rs182519871	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71986828	TCTTGAGTATATGGA[A/G]GCATTTCTGCAGTTA	55298
rs182533271	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968169	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	55298
rs182533642	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71950166	TGCTCAGCCAAAGAG[A/G]TGAAGGATTGGGTTT	55298
rs182634834	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928740	CTGAGGGAGCGTCGC[A/G]AAAGTTGCCCGTTTT	55298
rs182678449	snp	A/C			intron-variant	RNF121	GRCh38.p7	11:71986331	ACTAGCCTTCCCTGC[A/C]TGTTAATCTTCTGAG	55298
rs182679307	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71932859	GGTTTTTCCATACAG[C/G]TCCTTTAACTTACTG	55298
rs182697033	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949937	ACCTGGGAGGCAGAC[A/G]TTGCAGTGAGCCAAG	55298
rs182964142	snp	C/G/T			intron-variant	RNF121	GRCh38.p7	11:71967372	TTTTTTTTTTTGAGA[C/G/T]GGAGTCTCACTCTGT	55298
rs182984780	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71928545	TTTGAAAATGAGTCC[A/T]ACCGAGGCAAGATGG	55298
rs182985968	snp	A/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71988530	AAATCCTGGCCAGGT[A/G]TGGTGGCTCTCACTT	55298
rs183077143	snp	A/C	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71963624	ACTCCTTCCCAAAAA[A/C]AAAAGAGTTTTATAG	55298
rs183095668	snp	A/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71981780	TCTTACTTATCGGAA[A/T]TTATTGAGGACATAT	55298
rs183097244	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933701	ATTATAAAATTGTCT[A/G]CCTTCCTCACTAGAC	55298
rs183099854	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71963093	GTTAGAGTACTTTAT[A/G]TAATCTGGATAATAG	55298
rs183196293	snp	A/G	1.70035e-05	0.00291572	intron-variant	RNF121	GRCh38.p7	11:71982921	CAACCCCAAGGTGAG[A/G]GTTTAAGTAGTGGGA	55298
rs183198000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71944070	GGCACGGTAACTCAT[A/G]TCTGTAATCCCAGCA	55298
rs183200336	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71964207	GTTTTGTAGTTTTCA[A/G]TGTACAAGTCTTGCA	55298
rs183204516	snp	C/T	0.0119091	0.0762411	intron-variant	RNF121	GRCh38.p7	11:71992469	GTTTAGTGATGTCTT[C/T]GTGACAGAAATATGA	55298
rs183206381	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945879	GCACTTTGGGAGGCT[A/G]AGGAGGGTGGATCAC	55298
rs183256141	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71973987	TGCTCTTTCACCCAG[A/G]CCAGACTGCAGTGGC	55298
rs183320563	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981987	GGAAAGGAGACTAGA[C/T]GGAAGGCTTCGTGTG	55298
rs183349510	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71945092	TCCTGGGCTCAAGTG[A/G]TCCTCCTGCCTCAGC	55298
rs183358076	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71958211	CTTTAACTGGATCAT[A/G]TGTAGAAGAAGGCAA	55298
rs183363427	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938998	CAACCTTTGCCTCCC[A/G]AGTTCAAGCGATTCT	55298
rs183559886	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71953295	GCCTCAGACTCCCAA[A/G]GTGCTGGGATTACAG	55298
rs183574108	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993796	CTTAATTATGATAAT[A/G]CTTAAGTGAATATCT	55298
rs183583150	snp	A/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71974518	GTTTTCAGATTAGTA[A/G]ACCAAGGTACAGAAT	55298
rs183769759	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71973594	GAGTTCAAGACCAGC[C/G]TGACCAACATGGTAA	55298
rs183791116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933099	AAAAGCCAATCTACT[C/T]CTGGAGCTAGTGATT	55298
rs183797899	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930056	ATTAAAATACCAGTG[A/G]TCCTTGAAGGAATCA	55298
rs183808597	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71951736	TGAAAAGAAGTCCAA[C/T]GTCATTTAGCTGTCA	55298
rs183815846	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71930479	AGGGACTGAGAAATT[A/G]ACAGGTGATCACAGC	55298
rs183868843	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993138	CCTTTTTGAACAACT[C/G]TCTTGTGCTTTACCT	55298
rs183882781	snp	A/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71989761	GACTTGGACCAAAAT[A/T]TAACTTTGATGATAT	55298
rs183884423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71970009	TCACATCTTAGGTTC[A/G]TTTGTGGGTTCAGTA	55298
rs183888397	snp	A/C	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71954417	CAGCCTTAGTTCTTG[A/C]CCTTCCGAGCTGCCT	55298
rs183931561	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981036	ACTGGTCTAGAAATC[C/T]CTAAGAGTAAATACT	55298
rs183945062	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961007	AAAGACAATAACAAT[G/T]AACTTTATGTATGAA	55298
rs183946510	snp	C/T	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71968475	AGTTCTTCTGCCTGC[C/T]TAGGCATATTTTAGG	55298
rs183954725	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997029	CGTGGGCAGGGCTGT[G/T]GTCAGCCAAGAATAG	55298
rs183959624	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929419	GCTGGGTGTCTTAGG[A/G]TAGGACCGAAGGGCT	55298
rs184032037	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71955717	AGGTCCAAGTTGGAG[A/G]AGAAGAAGAAGAGTT	55298
rs184051285	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71935442	CAATATGAGTACTCT[A/G]TACTGTCCATCCTGT	55298
rs184114374	snp	A/G	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71950988	CCAGCACTTTGGGAG[A/G]CTGAGGTGGACGGAT	55298
rs184118409	snp	A/G	0	0	intron-variant	RNF121	GRCh38.p7	11:71977847	CATTAGCCAAGTCCT[A/G]GAGGGCCAAGGCTTT	55298
rs184248396	snp	C/G	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71966384	GATAGTTCTACAAGA[C/G]TTCAGAAGCAAAACA	55298
rs184389371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983976	CATAAGTTCCTCTCT[A/G]GCTTTGGTAGTTTAC	55298
rs184409097	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948251	CCAGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA	55298
rs184470828	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71980589	TGACCTAAGGTGATC[A/T]ACCTGCCTTGGCCTC	55298
rs184474260	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71960138	CCTTGAGCCTTTGAG[A/G]AGGCTGTTTACCTGT	55298
rs184525169	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989126	GTCTTGCTTTGTCGC[C/T]TAGGCTAGAGTGCAG	55298
rs184534876	snp	C/T	0.0107246	0.0724382	intron-variant	RNF121	GRCh38.p7	11:71951164	GGGAGGCAGAGGTTG[C/T]GGTAAGCCGAGATTG	55298
rs184567632	snp	A/C	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71979897	CTACTGTTTTGTAAA[A/C]AGCCCCATGAGCCTG	55298
rs184577464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71939779	TTATTTTCAAAAGTC[A/G]CTATGTATTTATTGT	55298
rs184650969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940960	TGCAAGGCTTGGAGA[C/T]GTTAAACAGCGTGGA	55298
rs184658369	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71969106	TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	55298
rs184701677	snp	A/G	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71959896	CGGCCTCAGCCTCTC[A/G]AAGTGCTGGGATTAC	55298
rs184725578	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71983408	AGGCCCTGCCATGGG[A/G]CCTGGCACATAGTAG	55298
rs184725835	snp	C/T			intron-variant	RNF121	GRCh38.p7	11:71937444	CAGCTTCTGGAGTAG[C/T]TGGGATTACAGACAC	55298
rs184727783	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71965075	CAAAAGTGTCCCAGA[A/G]GGAACCACTGTTAAT	55298
rs184809168	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956603	AATTCAGTTTGCCCA[C/G]GTCCAGTGTAGCCTA	55298
rs184965240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940300	TTGGAAAGATAGTGG[C/T]CATAATTCTAAAATA	55298
rs185086654	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972349	CATGAACTGTTTGAG[A/G]TTAGCCATTAGAGCT	55298
rs185094050	snp	C/T	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71981795	TTTATTGAGGACATA[C/T]CATATGCCAACAGTT	55298
rs185194114	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71991152	ACAGGATCATTCGCA[C/T]CCCAGACCTCAGTAT	55298
rs185226408	snp	C/G	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71976326	GTAGACCTGCTGCCC[C/G]CTCCATTCTGGGTAT	55298
rs185233155	snp	A/G	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71957712	TCATCATTATTATCC[A/G]TGATACAGGATGGGG	55298
rs185237145	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71938237	TTCTCCTATTTTAGT[A/G]ACAGGAATAGCTAAC	55298
rs185304890	snp	G/T	0.077417	0.180873	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996420	AAGACTCAAAGGGGT[G/T]CTTGGGCCACTCAGG	55298
rs185328843	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71994045	CGGGGTTTCACTGTG[C/T]TAGTTAGGATGCTCT	55298
rs185338509	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956018	AGGCCACCTTCAATA[A/G]TGATGGGCATTTCCA	55298
rs185356841	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71952904	TTTTGTGGTGACTAC[A/C]TTTGAAAATTCACTC	55298
rs185386986	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71947317	GTTTGTAGAGACCTC[A/G]TCTTTACAGAAAATA	55298
rs185438099	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71975429	CCCATCATGATGCCT[C/T]TTTCTATCTGGACCT	55298
rs185451814	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71975266	GAAGGAAAAACTTCT[A/G]TCTTCAGAATATAAC	55298
rs185464720	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71932387	GGAAGTACAGCTTCT[A/G]ATCCAGGCCTGCCTG	55298
rs185468267	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71936452	TGGAGCGCAGTGGCA[C/T]GATCTCGGCTCACTG	55298
rs185561766	snp	C/G	0.00597247	0.0543191	intron-variant	RNF121	GRCh38.p7	11:71992027	TGGAGACCAAGGTGG[C/G]AAGTCACTTGAGCCT	55298
rs185568725	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71972888	AACCTTCACATTAAG[A/G]GAAACATAGGCTGGG	55298
rs185570981	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71953214	AATTTATTTATTTTT[C/T]GTAGAGATGGGTTCT	55298
rs185571091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71994650	AAGGCCTGAGGTCTC[C/T]GTGGAGCTTCCTACT	55298
rs185584471	snp	C/T	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71932958	AGAGATGGGCCTAGC[C/T]AGCTCAGCTCAGGTA	55298
rs185773746	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71962739	ATTGCTGAGTCATGT[A/G]GTAACTCTGTGTTTA	55298
rs185778318	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71943223	TGGTGGATTGGATAT[A/G]TGATGTAAGGGAAAG	55298
rs185865757	snp	C/T	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71981621	TTCAAATTTCTGTCT[C/T]AGAGTTAGAATTGTT	55298
rs185943593	snp	A/G			intron-variant	RNF121	GRCh38.p7	11:71967539	ATTTTTAGTACAAAT[A/G]TATTTTAGTACAAAA	55298
rs185974538	snp	A/T	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71963255	TTTTATTGGTTGTGC[A/T]TTTAGTGTCATATCT	55298
rs185981404	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71991732	TGAGGAACTAAGACC[A/G]TTGCGGTTGTATGGC	55298
rs186024137	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948718	TCCAGCTGATTTATG[A/T]CTTTGGTGGCCTGAA	55298
rs186030120	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71926776	TGTGGTGGCACATGC[C/T]TGTAATCCCAGCTAC	55298
rs186070562	snp	C/T	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71986594	AATATGGTGAAACCC[C/T]GTCTCTACTAAAAAA	55298
rs186080937	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71950027	AGAACACACACACAC[A/G]CACACAAAACTCGCA	55298
rs186126609	snp	C/T	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71972598	ATAATTCTTTTTTTC[C/T]CGGGGGCTGTCCTGT	55298
rs186222097	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71981462	TCTTTGATTTTGTTG[A/G]TGGCATCAGGAAGAA	55298
rs186245279	snp	C/G	0.00517822	0.0506191	intron-variant	RNF121	GRCh38.p7	11:71942503	CACAGTGGCTCACGC[C/G]TGTAATCCCAGGACT	55298
rs186403194	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71961475	CTGAGAGGTGGGAAG[A/G]TTCCTTGAGCCTGGG	55298
rs186615187	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	IL18BP, RNF121	GRCh38.p7	11:71997600	TTGGAAAGCTGAACA[C/T]TTATCTTGCTTTCTT	55298
rs186664021	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71954623	TCTCTATTTTCTAGA[C/T]GGAGAAACTAAGCCA	55298
rs186669781	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71934671	GTCTTGGATATCTGA[C/T]TACCTCTGGATTTTT	55298
rs186684889	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71931126	AGGTGTGAGTCACCG[C/T]GCCCGGCTAAGAAAA	55298
rs186735599	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71974231	CAGGCGTGAGCCACC[A/G]CGCCCAGCCAAGCCC	55298
rs186780651	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996830	GTCCTCCCTCCCCCA[C/G]TGTCTGGGACACAGG	55298
rs186789865	snp	A/G	0.00438332	0.0466095	intron-variant	RNF121	GRCh38.p7	11:71957973	GACTATAAAAACATA[A/G]AATGGCAAAAATACC	55298
rs186889174	snp	C/T	0.00279162	0.0372561	intron-variant	RNF121	GRCh38.p7	11:71952179	TACAAAGTGGATGAA[C/T]CTTGAAAGAATTATG	55298
rs186997869	snp	G/T			intron-variant	RNF121	GRCh38.p7	11:71977165	CTTGGGCTTATAGTT[G/T]CATTTCATCCACTAT	55298
rs187015469	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71938571	TGATCCGCCTGCTTC[A/G]GCCTCCCAAAGTGCT	55298
rs187041964	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71985380	TTGTCTCAAAGAGGT[G/T]ATTTGACTTATCTGA	55298
rs187065075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71949101	CAAAGGTTGGGCTTA[C/T]TCCTCTTTAATGTTT	55298
rs187107729	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993904	GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC	55298
rs187137724	snp	A/G	0.00398564	0.0444627	intron-variant	RNF121	GRCh38.p7	11:71974527	TTAGTAAACCAAGGT[A/G]CAGAATCCTGAAGTG	55298
rs187143014	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71955777	ATTGTTATTTAGAAA[C/T]GTGATTCATAATTGC	55298
rs187253844	snp	G/T	0.0170251	0.090679	intron-variant	RNF121	GRCh38.p7	11:71967339	GGTAATAATTATGTG[G/T]GTTTTTTTTGTTTTT	55298
rs187262277	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927807	ATTTACAATATTCTC[C/T]GTATTAAGTGTCACA	55298
rs187477858	snp	A/G	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71983247	TAAATTAGATTTTCC[A/G]TTATATTCTGTCATT	55298
rs187492310	snp	A/G	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71964822	CAACCTGTCAGGAAT[A/G]TTGTGGAGGGGATGT	55298
rs187498629	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71945982	CAGACATGGTGGCTC[A/G]TTTCTGTAGTCCCTG	55298
rs187518509	snp	C/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71987343	TCATATTTTCCAAGG[C/G]TTTATATTTTAGTGG	55298
rs187522478	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71968206	CTGGGATTACAGGCT[C/T]CTGCCACCATGCCTA	55298
rs187531323	snp	A/C	0.0111196	0.0737302	intron-variant	RNF121	GRCh38.p7	11:71950738	GCTCACTGCAAGCTC[A/C]GCCCCCTGGGTTCAC	55298
rs187537564	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71929184	GGGGAGGGGCAGTGA[A/G]GTATCGGGAGGTGGG	55298
rs187585091	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71939471	GACTCTTAAAGTGAA[C/T]ATGAAGATTTTAATA	55298
rs187586254	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71959096	GATATACAGATGTGA[A/G]GTTAATTGGCCATGG	55298
rs187604631	snp	C/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71939007	CCTCCCGAGTTCAAG[C/T]GATTCTCCCACCTCA	55298
rs187671654	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71993182	ACCTATTTGTGTAGA[C/T]ATTGGATCTTCCTTT	55298
rs187718377	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71989289	TTTCACCATGCTGGC[A/G]AGGCTGGTTTCGAAC	55298
rs187834886	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71945380	TTAAACTTAGTAGCC[A/G]TTGGCTGTATCAGAT	55298
rs187845854	snp	A/G	0.00358779	0.0422022	intron-variant	RNF121	GRCh38.p7	11:71959697	ACGGAGTGCAGTGTT[A/G]CGATCTTGGCTGACT	55298
rs187898945	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	IL18BP, RNF121	GRCh38.p7	11:71997337	CCCTACATGATTTTT[A/G]TCATTCATGGGTCCT	55298
rs187899915	snp	C/G			intron-variant	RNF121	GRCh38.p7	11:71944192	CAAAAAATTAGCCAG[C/G]CGTGGTGGCATGCAC	55298
rs187902964	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71978057	AAAGTAGAAACTGAA[A/G]AAAATTTTTTGTATT	55298
rs188107954	snp	C/G	0.00478085	0.0486577	intron-variant	RNF121	GRCh38.p7	11:71969136	AGGTGATCCACCTGC[C/G]TCGGCCTCCCAAAGT	55298
rs188112444	snp	C/T	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71982422	ACATGGTGAAGATTT[C/T]GTGTTCGAGATACCA	55298
rs188116076	snp	A/C	0.00159617	0.0282053	intron-variant	RNF121	GRCh38.p7	11:71951550	AGGATTGCTTGAGCC[A/C]AGGGATTTGAGGCTC	55298
rs188124461	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF121, LOC100133315	GRCh38.p7	11:71930092	AGGAAGGAGATGTTG[A/G]GTGTGAAAGGAATGA	55298
rs188341542	snp	A/C/G/T	0.000439186	0.0148131	utr-variant-3-prime, nc-transcript-variant, upstream-variant-2KB	RNF121, IL18BP	GRCh38.p7	11:71996350	AAAACCCACCCCACA[A/C/G/T]GCCATGGACCTCAGG	55298
rs188343302	snp	C/T	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71975665	TTCCCCAGTCATTAG[C/T]ATGGCATCCAGTAAG	55298
rs188349740	snp	C/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71956702	TCATACTTTTTGCTC[C/T]AGCCATACTCAATTG	55298
rs188354641	snp	C/G	0.0115144	0.0749975	intron-variant	RNF121	GRCh38.p7	11:71973746	GAGTCAAGATCCTGC[C/G]ACTGCACTCTAGCCT	55298
rs188359371	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71937587	AATGATAGCGAACTA[A/G]TCGTTCCATGGTCAG	55298
rs188372137	snp	A/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71933202	TGGGAATTAAGGTAA[A/T]AAAGCACTTCAATAC	55298
rs188398737	snp	C/T	0.0232847	0.105357	intron-variant	RNF121	GRCh38.p7	11:71935852	ATTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	55298
rs188402775	snp	G/T	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71963913	ATTGTTATGATTACT[G/T]TAGCACTGTAGTAAG	55298
rs188474839	snp	A/C	0.00318978	0.0398085	intron-variant	RNF121	GRCh38.p7	11:71959897	GGCCTCAGCCTCTCA[A/C]AGTGCTGGGATTACA	55298
rs188633323	snp	A/C	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71992964	CCCAAGACCCCACCC[A/C]AAGAAGGAATATTTC	55298
rs188651902	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71954015	CCTAGTTGGGGAGCA[A/G]TTGGCTAGCATTAAG	55298
rs188658716	snp	A/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71948604	GGGTAAAGGGCAGGC[A/G]GCAGCTGTAGCAGCT	55298
rs188666215	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71940023	GAAGACTTCCGATAG[A/G]GTATGGCATTTAGGC	55298
rs188742030	snp	A/G	0.00199481	0.0315187	intron-variant	RNF121	GRCh38.p7	11:71979994	CATGAGTTGGGTTGC[A/G]TTTTCCCCAAATTTA	55298
rs188759211	snp	G/T	0.00119737	0.0244387	intron-variant	RNF121	GRCh38.p7	11:71984911	ACATTTGATAGTGCT[G/T]TACAATTTCAAAGCA	55298
rs188776246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF121	GRCh38.p7	11:71948733	ACTTTGGTGGCCTGA[A/G]AGGTGAGGTTTCCAC	55298
rs188784492	snp	C/T			upstream-variant-2KB, intron-variant	RNF121, LOC100133315	GRCh38.p7	11:71927165	AGGTGGGAGAATTGC[C/T]TGAGCCTGGGAGATG	55298
rs188896634	snp	C/G	0.000798403	0.0199641	intron-variant	RNF121	GRCh38.p7	11:71988769	CAAGGCTGCAGTGAG[C/G]TATGATTGTGCCACT	55298

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