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

RNF123

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs4768	snp	C/T	0.392426	0.205462	downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721331	GTTCAAAGGTGGAGG[C/T]TCCAGGATGGCACAG	63891
rs1046598	snp	C/T	0	0	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721611	TTGGACACCTGCCTT[C/T]TCATGTGGACATCAT	63891
rs1491985	snp	C/G	0.250354	0.25	intron-variant	RNF123	GRCh38.p7	3:49702074	TCCACCACTGGAGGT[C/G]AGGTGAGGAACATGG	63891
rs1491986	snp	A/G	0.486889	0.0798969	intron-variant	RNF123	GRCh38.p7	3:49701653	AGATGCCCAGGCCAG[A/G]GGCCTTGCCATGACC	63891
rs2087730	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689378	CCGACCTCCGCCTGC[C/T]CTGGGGATGCTCCCA	63891
rs2291542	snp	A/G	0.395346	0.203408	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49714152	GCTGGGCAAATTGGC[A/G]TCCTCAAGTTTGGTT	63891
rs2291544	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720961	GCTATGTGGATGTCC[A/G]TTGTGCCTGTGTAGG	63891
rs2329012	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689485	GGCTGGGCGCGGGCC[A/G]GTGCGCGTGCGCGGC	63891
rs2329013	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689557	ACGGACGCCGTAGCC[A/G]AGAGGTTGGGCGGAT	63891
rs2329014	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689580	GGGCGGATGTTGTGA[A/G]CCGGGTCGCTGCGGC	63891
rs2329015	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689590	TGTGAGCCGGGTCGC[G/T]GCGGCCGAGGCTCCG	63891
rs2329016	snp	A/G	0.277778	0.248452	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689708	CAGCGCAGGGATCTG[A/G]GTGCGAAACTCCGAG	63891
rs2329017	snp	C/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696245	CGGACAGGTTATGTG[C/G]TATGCAGACAGCACT	63891
rs2329018	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49696409	actagagtgcagtgg[C/T]acgatcatggctcac	63891
rs2329019	snp	A/G	0.00597247	0.0543191	intron-variant	RNF123	GRCh38.p7	3:49696410	ctagagtgcagtggc[A/G]cgatcatggctcact	63891
rs2876714	snp	C/G/T	0.000548415	0.0165518	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687473	TGATGCAGGTCCGTA[C/G/T]GTAGTCTGGGAGCAA	63891
rs2876716	snp	C/G	0	0	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689604	CTGCGGCCGAGGCTC[C/G]GGGTGAGTGAGGGGC	63891
rs2933246	snp	C/T	0	0	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689548	ACCTCTTGGCTACGG[C/T]GTCCGTTCAGGGCCA	63891
rs2960545	snp	C/T	0.467744	0.122832	intron-variant	RNF123	GRCh38.p7	3:49692625	cttggaagggtagta[C/T]agggcttgtggggag	63891
rs2960546	snp	C/G	0	0	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691494	CTGCTGGTGGCTGCT[C/G]GGGGTGCATGTTCAG	63891
rs2960547	snp	C/G	0	0	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690409	TCACTGATGTGTAGc[C/G]gtgctgtccaacaca	63891
rs3020779	snp	A/G	0.244462	0.249939	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687375	GAGCCACAAGTTCCC[A/G]AATGATCACAAGTGA	63891
rs3201833	snp	A/C	0.0198	0.0975087	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720000	AGGCTCAGGCGAACC[A/C]CCTTAAGATAGTGAG	63891
rs3749240	snp	A/T	0.483121	0.0903023	intron-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49712755	CCCGCCCCCCACAGA[A/T]GTGTGTTGCTGGGCC	63891
rs3749241	snp	C/T	0.481087	0.0953875	intron-variant	RNF123	GRCh38.p7	3:49706959	AGGGCCCTGGCACAA[C/T]CTTGCTAGACCCGTG	63891
rs3872334	snp	A/G	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689339	GCGGCAGAACGCGAC[A/G]TGCTAACCGGAATCC	63891
rs3872335	snp	G/T	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689272	CGCTCAGACGGTCCT[G/T]AAAACGTCTGAAAGG	63891
rs3872336	snp	C/G	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689255	AAACGTCTGAAAGGC[C/G]GTTCCTGCCAGAGTC	63891
rs3966647	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49691785	CTGGCACCTACTCCA[C/T]ACCCAGCATCTGCCC	63891
rs4052554	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49691912	AAGTTTAATACTTTT[A/G]AGTGTAGTCAGTATA	63891
rs4052555	snp	A/G	0	0	intron-variant	RNF123	GRCh38.p7	3:49691925	TTAAGTGTAGTCAGT[A/G]TAAAAGTTACAAGTA	63891
rs4052556	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49692065	cctgagcaacatggc[A/C]agaccccatctctac	63891
rs4052557	snp	C/T	0	0	intron-variant	RNF123	GRCh38.p7	3:49695958	GCTCGGGTAGGTGGG[C/T]CATGTGCTCCGCTGA	63891
rs4052558	snp	C/T	0.00970851	0.0689927	intron-variant	RNF123	GRCh38.p7	3:49695968	GTGGGTCATGTGCTC[C/T]GCTGACCATTTATGG	63891
rs4052559	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49696046	CTTTCATACTTCCAG[A/G]ACATGTCCCATTCAA	63891
rs4052560	snp	A/C	0	0	intron-variant	RNF123	GRCh38.p7	3:49696213	CCAGACATCATCAGC[A/C]CAGCCACCTTTGAGA	63891
rs4052565	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689122	GGCAGGTCAGCCCAC[A/G]CCCGGCGGCAGAGCC	63891
rs4052568	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689295	TCTGAGCGGGGCCTC[C/T]AAGTATGGGTAGGAG	63891
rs4052570	snp	C/T	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689449	CCCGGTGGGAAGCCA[C/T]GGAGGGGGTCCCCTA	63891
rs4052571	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant	MST1, RNF123	GRCh38.p7	3:49689517	GGAGGCTCAGCGCGC[A/G]AGCGTGCGCGTGATT	63891
rs4855841	snp	C/T	0.489492	0.0717183	intron-variant	RNF123	GRCh38.p7	3:49708244	gggcacagtggcgca[C/T]gcctgtaaccccagc	63891
rs4855862	snp	A/G	0.485799	0.0830599	intron-variant	RNF123	GRCh38.p7	3:49711400	CAGACAGAGACCCTG[A/G]TGAGACTATTTCAGA	63891
rs4855865	snp	C/T	0.28578	0.247426	intron-variant	RNF123	GRCh38.p7	3:49709609	tctactaaaaaaaaa[C/T]acaaaattaggccag	63891
rs4855867	snp	A/G	0.485799	0.0830599	intron-variant	RNF123	GRCh38.p7	3:49708389	tgtcagggaagctgg[A/G]gaagggaggacagga	63891
rs4855880	snp	C/T	0.482979	0.0906686	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688252	GCCTAGCCAGGGCCC[C/T]TGGCTGGGTAATGTG	63891
rs6414619	snp	A/G	0	0	intron-variant	RNF123	GRCh38.p7	3:49695416	GTAACTGCTTTTGAG[A/G]AAGGCTCCTTTATCC	63891
rs6414620	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49695703	TCTGTGTGGATGAGT[A/G]GGGTAAGAACTGGCA	63891
rs6446288	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692192	tgaggctgcagtgag[C/T]tggcctctgcatgcc	63891
rs6446290	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49695709	TGGATGAGTGGGGTA[A/G]GAACTGGCATTAAAG	63891
rs6446291	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49695720	GGTAAGAACTGGCAT[G/T]AAAGGTGGAAGAGCA	63891
rs6446292	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49695746	GAGCAGGTGGTGGCA[C/G]CCTGTGGGCAGCCAG	63891
rs6785549	snp	A/G	0.486389	0.0813663	intron-variant	RNF123	GRCh38.p7	3:49699132	TGAAGATGGCTGTGG[A/G]CTGCTCAGAAGCTCT	63891
rs6793046	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49695727	ACTGGCATTAAAGGT[A/G]GAAGAGCAGGTGGTG	63891
rs6802347	snp	C/G	0	0	intron-variant	RNF123	GRCh38.p7	3:49695516	CTGCATAGCCACCAC[C/G]TGGCCTTGGCCTGGG	63891
rs6804655	snp	C/T	0.392752	0.205236	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701512	CGTGCTCCGCTCCGT[C/T]GTCTTCTTTTACATC	63891
rs7372727	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690581	TGTGTGAGTGGGAAT[A/G]GTGAAACTATCAGGA	63891
rs7372747	snp	A/G	0	0	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690774	CTTACAACTGAGATG[A/G]ATACAGGGGCTCTGC	63891
rs7373000	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49692216	gcatgccactgcact[C/G]tagcctgggtgacag	63891
rs7373192	snp	C/T			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690453	GACTCAGTGCAGGTT[C/T]TGGAGCAGCTGCAGC	63891
rs7373388	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690857	CATTTTGTTATGGTT[C/T]GGCAAAAATATATCT	63891
rs7373396	snp	C/G	0.277778	0.248452	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690967	GACCCTGGCTACCCT[C/G]CCTGTGTAGGAAGCT	63891
rs7373406	snp	C/T			intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691004	CCCTGCATTCCCCTG[C/T]CCTATGTGTTAGTGT	63891
rs7373640	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49691713	CAGTGCTAGTTCCTT[C/G]TGAGAGTCAGGGAGC	63891
rs7373744	snp	A/G			intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690873	GGCAAAAATATATCT[A/G]GTACCTGCTCTCTGC	63891
rs7373910	snp	C/T			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690580	ATGTGTGAGTGGGAA[C/T]GGTGAAACTATCAGG	63891
rs7373923	snp	C/T			intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690767	AGTATGGCTTACAAC[C/T]GAGATGGATACAGGG	63891
rs7374215	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692305	ATGACTATTCAAATG[C/T]GATTCTTTTCTGTTT	63891
rs7375140	snp	C/T	0	0	intron-variant	RNF123	GRCh38.p7	3:49695666	TGCTTGTCCAACCTT[C/T]GTCCCCTTCCAGAGC	63891
rs7432489	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49695193	ctgcaacctcaaagt[C/T]ccaggctcaaggaat	63891
rs7432997	snp	A/C	0	0	intron-variant	RNF123	GRCh38.p7	3:49695932	CAGACAGATTTTTCC[A/C]AACTCCTTTGGCTCG	63891
rs7433063	snp	C/T	0.375	0.216506	intron-variant	RNF123	GRCh38.p7	3:49696303	CTCTAACATAAGTCA[C/T]TATTCTGTTTTTACA	63891
rs7433242	snp	A/G	0	0	intron-variant	RNF123	GRCh38.p7	3:49695146	CTGttttcttttgag[A/G]cagggtctcgctatg	63891
rs7433245	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49695164	gggtctcgctatgtc[A/C]cagtcatagctcact	63891
rs7433259	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49695287	ttttttttttaagag[A/G]cagggtcttactgtg	63891
rs7433792	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49695303	cagggtcttactgtg[G/T]cacccaggctggtct	63891
rs7628207	snp	C/T	0.25634	0.24992	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717537	ACTCCTCGAGAGCTG[C/T]CTCAGCCCCTGAGGG	63891
rs7634466	snp	C/T	0	0	intron-variant	RNF123	GRCh38.p7	3:49692391	tatatttatagggta[C/T]atgagatactttgat	63891
rs7634945	snp	A/G	0.0095466	0.0684263	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720678	CTGGTGGGGCAGGTC[A/G]GGGAAATCTGGGGCT	63891
rs9852529	snp	A/G	0.314301	0.241589	intron-variant	RNF123	GRCh38.p7	3:49693192	tagctgggactgcag[A/G]tgcccgccaccatgc	63891
rs9856961	snp	A/G	0	0	intron-variant	RNF123	GRCh38.p7	3:49693627	gtcccaaagtgctga[A/G]attacaggcatgagc	63891
rs9858213	snp	G/T	0.314301	0.241589	intron-variant	RNF123	GRCh38.p7	3:49694428	CTGAGCATCTTTAGG[G/T]CCAGGGGGTCTGCTG	63891
rs9872539	snp	A/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49693378	tttttttttttgaga[A/T]ggagttttgctcttg	63891
rs9873183	snp	A/G	0.489492	0.0717183	intron-variant	RNF123	GRCh38.p7	3:49696796	GGATTATACGCATGC[A/G]CCACCACACTCAGCT	63891
rs10632591	in-del	-/CAA			intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720160	CTAAAAATACAACAA[-/CAA]TTAGCCGGGCGTGGT	63891
rs11130214	snp	C/G	0.3748	0.216622	intron-variant	RNF123	GRCh38.p7	3:49698313	GCTCAGAGAATACCT[C/G]TTACTCTTTCCCTCA	63891
rs11130216	snp	A/C	0.393665	0.204598	intron-variant	RNF123	GRCh38.p7	3:49698739	GTGCATCTGGTGAGG[A/C]CTCCTCTCATGGCAG	63891
rs11130217	snp	A/G	0.237882	0.249706	intron-variant	RNF123	GRCh38.p7	3:49699890	CAGCATCACCTGGCG[A/G]GGGCCCCATGTGACC	63891
rs11130218	snp	C/T	0.489318	0.0722982	intron-variant	RNF123	GRCh38.p7	3:49714939	ATTGCCGTGGTCCTG[C/T]GTCCAGGGCGGAACT	63891
rs11130219	snp	C/T	0.485596	0.0836329	intron-variant	RNF123	GRCh38.p7	3:49714994	GGGGCCAGGCCTGTC[C/T]TGCTGCTGCGGGAAC	63891
rs11309936	in-del	-/G	0.4776	0.103433	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688000	GGATCAAAGCTACAA[-/G]GCTTCTGGGATGGAC	63891
rs11436625	in-del	-/G			intron-variant	RNF123	GRCh38.p7	3:49695603	GGAGTGGCTTACACT[-/G]GGGGAATATGTGATC	63891
rs11447161	in-del	-/T			intron-variant	RNF123	GRCh38.p7	3:49696661	ACCTGGCCACATACT[-/T]TTTTTTTTTTTTTTT	63891
rs11706368	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49710486	ggtttcaccttgttg[G/T]tcaggctggtctcaa	63891
rs11709680	snp	C/T	0.485664	0.0834419	intron-variant	RNF123	GRCh38.p7	3:49707755	CACCTTTTTCCCATT[C/T]GTGACTCTCCTGCTA	63891
rs11709734	snp	A/G	0.257176	0.249897	intron-variant	RNF123	GRCh38.p7	3:49707802	TTACTGCCCCATGAC[A/G]GGAACTTCCTCTCCC	63891
rs11709749	snp	C/G	0.0115144	0.0749975	intron-variant	RNF123	GRCh38.p7	3:49708038	GTTGCCCAGGCTGGA[C/G]TGCAATGGCATGATC	63891
rs11710398	snp	A/T			intron-variant	RNF123	GRCh38.p7	3:49710480	agatggggtttcacc[A/T]tgttggtcaggctgg	63891
rs11710400	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49710487	gtttcaccttgttgg[G/T]caggctggtctcaaa	63891
rs11710675	snp	A/C	0.375797	0.216044	intron-variant	RNF123	GRCh38.p7	3:49714467	CACCATGTTCCTGGC[A/C]TGCTACAGCTCATGC	63891
rs11714024	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49710477	tagagatggggtttc[A/G]ccttgttggtcaggc	63891
rs11716575	snp	A/G	0.485731	0.0832509	intron-variant	RNF123	GRCh38.p7	3:49707457	AGCCTGGTCAGATAC[A/G]TGGATGGACAGACAG	63891
rs11720705	snp	A/G	0.250608	0.249999	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716355	CCTTGAAGCAGGAGC[A/G]TGTGGGTGGCTCATC	63891
rs12381242	snp	C/T	0.489492	0.0717183	intron-variant	RNF123	GRCh38.p7	3:49709386	gctcactgcaagctc[C/T]gcctcccgggttcac	63891
rs12496226	snp	G/T	0.373799	0.217195	intron-variant	RNF123	GRCh38.p7	3:49696607	CTCCCAAAGTGCTGG[G/T]ATTACAGGCATGAGC	63891
rs12497499	snp	A/T			intron-variant	RNF123	GRCh38.p7	3:49699596	TGGTGAGCTGGGGTC[A/T]GGGCCAGGCGGGGTG	63891
rs12715437	snp	C/T	0.23846	0.249734	intron-variant	RNF123	GRCh38.p7	3:49714423	CCCTTTGGGCCTGGA[C/T]GCTCTATGTGGGTCA	63891
rs13061156	snp	C/T	0.0437281	0.141251	intron-variant	RNF123	GRCh38.p7	3:49710127	aggcatgagccacca[C/T]acccggcaatttcta	63891
rs13082499	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49695583	TGCTCCTACAGCTCA[A/G]GGCTGGGAGTGGCTT	63891
rs13325326	snp	A/G	0.00993419	0.0697739	intron-variant	RNF123	GRCh38.p7	3:49714542	CTCCAGCCTTGTCCC[A/G]GCACCATGTCCTTCT	63891
rs28537122	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49691992	TTCACACCTGTAATC[C/G]CAGCACTTTGGGAGG	63891
rs34057616	snp	A/G	0.0112201	0.0740552	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718038	AGGGTTGTAGAGATC[A/G]AATTCCTCAGCTACT	63891
rs34127462	snp	C/T	0.00618831	0.0552799	downstream-variant-500B, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721064	CTGCTATGCCCACCC[C/T]ATCTCTGCTGTGTTC	63891
rs34128749	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49699929	CAGACCTCAGTCAGT[-/C]CCCTAGGGAAACAGG	63891
rs34154145	snp	C/T	0.000181901	0.00953506	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49704674	CTTCCAAAGCCAACA[C/T]TGTGATCGACCCACT	63891
rs34261514	in-del	-/C	0.364193	0.222396	intron-variant	RNF123	GRCh38.p7	3:49708508	CCAGCGGCTCACAGA[-/C]CCCCCAGCTGGGCCT	63891
rs34317316	in-del	-/G			intron-variant, frameshift-variant	RNF123, AMIGO3	GRCh38.p7	3:49718048	AGATCGAATTCCTCA[-/G]CTACTGCCAGCTGCA	63891
rs34324674	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49701002	ACTTTTGTTCATGTT[-/C]CCACAGTGGGGATTC	63891
rs34379671	snp	C/T	0.011569	0.0751708	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700227	CTGGCCTTGGTGCAG[C/T]GCAAGGTGTATCTGG	63891
rs34539806	snp	A/G	0.044462	0.142317	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705151	AGTGAAGGTCCGCAC[A/G]CTGAGCGTGGAGCAG	63891
rs34614773	snp	G/T	0.486988	0.0797579	intron-variant	RNF123	GRCh38.p7	3:49715570	CGCCTCCTGTCCCCC[G/T]GCAGAGCCCTGCCCT	63891
rs34615189	in-del	-/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688693	ACCACAGCCCCATCC[-/G]GGGAAGTTGTGAAAC	63891
rs34713511	in-del	-/G			intron-variant	RNF123	GRCh38.p7	3:49709412	TCACACCATTCTCCT[-/G]GCCTCAGCCTCCCGA	63891
rs34810303	snp	C/T	3.37302e-05	0.00410658	intron-variant, stop-gained	RNF123, AMIGO3	GRCh38.p7	3:49718533	CTGCTGCGGCGAAAC[C/T]CAGGCAATGCGCATG	63891
rs34821039	in-del	-/T			intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717346	GAAGCTTTCAGGAGG[-/T]TTGGGTGTTGGTGGA	63891
rs34823813	snp	A/G	0.141261	0.225113	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712543	TTGAGCACGGTGATC[A/G]CACAGGGTCTCTCTT	63891
rs35072697	in-del	-/G			frameshift-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49705007	CAGGCCCTGGCTGTT[-/G]GGGGGGCCACTGCCC	63891
rs35074575	in-del	-/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696642	CACCTGGCCACATAC[-/T]TTTTTTTTTTTTTTT	63891
rs35201844	snp	A/G/T	0.00597445	0.054328	intron-variant, missense, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718779	CCAGCGCTGTAGCAG[A/G/T]TGGTAGAGGCGGCAG	63891
rs35261769	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49700035	ACTGCGTGTGCCAAG[-/C]CTTAGAGGAGCCGTG	63891
rs35299211	in-del	-/C			intron-variant, frameshift-variant	RNF123, AMIGO3	GRCh38.p7	3:49718900	GGTTGGAGGAGAGGT[-/C]CCAGAGTAAGCAGGT	63891
rs35382348	in-del	-/C			intron-variant, frameshift-variant	RNF123, AMIGO3	GRCh38.p7	3:49719313	TGGCACGTCCTGCAG[-/C]CCTAGGCCAGTGCAG	63891
rs35440223	in-del	-/C			frameshift-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49703488	CTTTGACCTGCAGCG[-/C]CTGGGGGGCCTCCTC	63891
rs35504478	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49706253	GCCTGTGCCTAGGTG[-/C]CCCCCCACCCCCTGG	63891
rs35528046	in-del	-/G			intron-variant	RNF123	GRCh38.p7	3:49694479	TTTGGAAGGACTTTT[-/G]GCTTTTGTAAACAAT	63891
rs35542238	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49705802	GCATGGGAGCACATG[-/C]CTCAGCGAGGCTGGT	63891
rs35620248	snp	A/G	0.0944542	0.195718	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700521	TGATGTCTCTGCTTC[A/G]GCTGTACCGATTCTC	63891
rs35726701	snp	A/G	0.0305034	0.119671	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49703462	GTCTTCTATAATGGC[A/G]AGGTGGACTACTTTG	63891
rs35877975	in-del	-/G			intron-variant	RNF123	GRCh38.p7	3:49698620	GACTACAGGGCACCA[-/G]GGGAAGGGTCAGGGA	63891
rs35885157	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49696041	GAGCCTTTCATACTT[-/C]CCAGAACATGTCCCA	63891
rs35926560	snp	C/T	0.00641528	0.0562715	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719078	GCGCCCCCAGCCCGT[C/T]GAGGTCGTGGCGGCC	63891
rs35938648	in-del	-/T			intron-variant	RNF123	GRCh38.p7	3:49693348	CCAGTGTGCCTGGCC[-/T]TTTTTTTTTTTTTTT	63891
rs36012302	in-del	-/A			intron-variant	RNF123	GRCh38.p7	3:49692516	CTTTTAGTTATTTTT[-/A]AAATGTACAATTATT	63891
rs41291702	snp	A/T			missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687151	CGGCGCCGCTTACCC[A/T]CCCGGCAGGATTTGA	63891
rs41291704	snp	A/C/G	1.672e-05	0.00289132	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687206	CAGGGTCTGTTGTGT[A/C/G]GCACCAAGGACCTCC	63891
rs41291706	snp	A/C			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687273	CAGGCCATTCCGGAG[A/C]GTGGGCGTGTACCTG	63891
rs41291708	snp	A/G			missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687280	TTCCGGAGAGTGGGC[A/G]TGTACCTGAGGGCCC	63891
rs41291710	snp	C/T	1.66643e-05	0.0028865	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687328	TGTGCTGGGGGAAGG[C/T]CCCAGGCCGGGACGG	63891
rs41291712	snp	A/G	6.6357e-05	0.0057597	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687404	TCCAAGCCTGGCAGG[A/G]CAGGCCACCCACGGT	63891
rs55662945	snp	C/T	0.0592355	0.161582	intron-variant	RNF123	GRCh38.p7	3:49695266	TGCCACAGCACCCAG[C/T]TAATTTTTTTTTTTT	63891
rs55816606	snp	A/C/T	0.000894195	0.021126	synonymous-codon, intron-variant, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721956	ACCCAGCCCAGCCCA[A/C/T]AGGCTTACCCACTGA	63891
rs57447277	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49702465	TACACATGCCATGCC[A/C]TCAGCACCTGGCACT	63891
rs57982862	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49713163	GCTGTCAGGCCCCTA[A/G]CCTGCCCCCTGCCCA	63891
rs61415571	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49709142	GTGATTTTTTTTTTC[C/T]TTTTTTGAGGTGGAG	63891
rs61743872	snp	C/T	0.000264738	0.0115021	missense, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716468	TCCTGGTGCGTGGCC[C/T]AGCCTCAGAGTGAGT	63891
rs61745258	snp	C/T	0.00407692	0.0449649	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702671	TGAGTACATGGTCTG[C/T]TTCTTACACCGGCTG	63891
rs61760878	snp	A/G	9.79024e-05	0.00699583	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713534	AAGAGACCCTGACCC[A/G]CCTGGCTGCCATTCT	63891
rs62262685	snp	C/T	0.494957	0.0499584	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688595	AGGGTTGGGGGCACT[C/T]ACCAGGGACCCCTAA	63891
rs62262686	snp	A/G	0.478686	0.101008	MST1, RNF123	3	allele_origin=G(germline)/A(somatic)	3:49688637	GAAGCAGCAGGAGTG[A/G]GAGCCACCCCATCCT	63891
rs62262718	snp	A/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49695268	CCACAGCACCCAGCT[A/T]ATTTTTTTTTTTTAA	63891
rs62262719	snp	A/C	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49707682	TTGGTATCCCCATTT[A/C]TATCATCTCTGCTTG	63891
rs62262720	snp	C/G			intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718392	CTGGTTGTGGTGCAG[C/G]CGGGGCCCAGTGGCC	63891
rs62640368	snp	A/C/T	3.42843e-05	0.00414019	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718243	GCACGGCGGCAGCAG[A/C/T]GGCAGGGTGGGGCGA	63891
rs71324988	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49693541	TTGGTATTTTTAGTA[A/G]AGATGGGGTTTCGCC	63891
rs71324989	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49697284	CGTAGCGGGCCTGGA[A/G]ACGTCTGGTGAGCTC	63891
rs71324990	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49697470	GGGGTGAGTGAGGGT[A/G]AGGTGTGGAGACCCA	63891
rs71324991	snp	C/T	1.65647e-05	0.00287786	missense, intron-variant, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721937	ACTCCCCGCCCCTCT[C/T]CCCACCCAGCCCAGC	63891
rs72936043	snp	A/C	0.0185938	0.0946107	intron-variant	RNF123	GRCh38.p7	3:49711416	CAGGGTCTCTGTCTG[A/C]CCCCATCTCAATCCG	63891
rs73077157	snp	A/C	0.121022	0.21416	intron-variant	RNF123	GRCh38.p7	3:49712272	TCTGGCCTGGGTCAC[A/C]GTAATGCGCCCTCCA	63891
rs73834010	snp	A/C	0.00556925	0.0524748	intron-variant	RNF123	GRCh38.p7	3:49702309	TTCTCAGCTCAGCAC[A/C]GCCTCACTTTTCCCT	63891
rs74439046	snp	A/C	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49712216	GGGTGACTCCATCTC[A/C]AAAAAAAAAAAAACT	63891
rs74462720	snp	A/G	0.0260105	0.111035	intron-variant	RNF123	GRCh38.p7	3:49700085	CCTCAGTCAGACCCC[A/G]GAAGGGGTCATCTAT	63891
rs74470696	snp	A/C	0.00323779	0.040105	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698108	GGCAGCTGATGGTGC[A/C]CCAGCCGATCTGCAT	63891
rs74643638	snp	A/C	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49712217	GGTGACTCCATCTCA[A/C]AAAAAAAAAAAACTT	63891
rs74680554	snp	C/G/T	0.00456467	0.0475558	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716493	GTGAGTGTTGGGGAC[C/G/T]GTGGGCCCCTGTGGG	63891
rs74898056	snp	C/T	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688161	CAGATCTAACACATA[C/T]GCTCTGTGAGAGCAG	63891
rs74914221	snp	G/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49714568	CTTCTGCTTCTTTTT[G/T]GCTATCTGCTGGTGG	63891
rs74944821	snp	C/G	0.00336427	0.0408756	downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721347	CCTCCACCTTTGAAC[C/G]CAGAGCCAGGCTGGG	63891
rs74956716	snp	G/T	0.0260105	0.111035	intron-variant	RNF123	GRCh38.p7	3:49698374	GCATCCAAGGCTGGT[G/T]ATTGGTGGGCTCTGG	63891
rs74959466	snp	C/G	0.00303423	0.0388318	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720606	AGCCCCCAGCACCTG[C/G]CACTGCTCTGCCAGC	63891
rs74982520	snp	A/G	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688477	TGTGCTCAAGAGGGC[A/G]AGGTCACTGCCCCAT	63891
rs75180045	snp	A/C	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688432	GAGGCCTAAGTGGGC[A/C]ATGTCTATGTGTTCC	63891
rs75277930	snp	A/G	0.0178098	0.0926698	intron-variant	RNF123	GRCh38.p7	3:49712183	GTGAGCCAAGAGGGC[A/G]TCACTGCACTCCAGC	63891
rs75428743	snp	A/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49695270	ACAGCACCCAGCTAA[A/T]TTTTTTTTTTTAAGA	63891
rs75572071	snp	G/T	0	0	intron-variant	RNF123	GRCh38.p7	3:49696364	CTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTT	63891
rs75721665	snp	A/G	0.00478085	0.0486577	intron-variant	RNF123	GRCh38.p7	3:49707087	CTGTGGACTGAGGAA[A/G]CGCAGTTTCTGGACC	63891
rs75811992	snp	A/G	0.00993419	0.0697739	intron-variant	RNF123	GRCh38.p7	3:49699942	GTCCCCTAGGGAAAC[A/G]GGGACATTGCCAACC	63891
rs75965871	snp	A/G	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688301	GGCTCTCACCTGCAC[A/G]AAGGCATATGCTAGG	63891
rs75976238	snp	C/T	0.00114849	0.0239359	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687869	TGTGCCCCGGAGCAC[C/T]TGGAAGTCATTCAAT	63891
rs75993402	snp	A/G	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688304	TCTCACCTGCACAAA[A/G]GCATATGCTAGGTTA	63891
rs76100153	snp	C/T	0.0232847	0.105357	intron-variant	RNF123	GRCh38.p7	3:49703017	TTTCTTCCGTCCTTG[C/T]CCCCCCATTTCTCTG	63891
rs76210323	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688186	GAGCAGTGGGTGATG[A/G]AGCTTGCCCCACCTC	63891
rs76363176	snp	C/T	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688310	CTGCACAAAGGCATA[C/T]GCTAGGTTAGAGGGG	63891
rs76570343	snp	A/G	0.00914312	0.0669923	intron-variant	RNF123	GRCh38.p7	3:49712371	GAAATCCAGGTCTCA[A/G]TTGTGCTGTCGTAGG	63891
rs76646787	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688124	CACCGGTGCCTCTGT[G/T]TAGTGGCCCAGGCAC	63891
rs76705346	snp	C/G	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688475	GCTGTGCTCAAGAGG[C/G]CAAGGTCACTGCCCC	63891
rs76989089	snp	C/G	0.0557024	0.157316	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705577	GCTGCTGGGGCGGCC[C/G]CCCGAGGAGCCTGAG	63891
rs77162577	snp	C/T	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688295	AATCTGGGCTCTCAC[C/T]TGCACAAAGGCATAT	63891
rs77208503	snp	C/T	0.0520825	0.152737	intron-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49712828	ACGTCTGCACCCTGC[C/T]CTGGGACCTGCAGCC	63891
rs77231150	snp	A/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49709307	CAGCTAATTTTGTAT[A/T]TTTTTTTTTTTGAGA	63891
rs77308703	snp	C/T	0.00477753	0.0486409	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699104	GGCAGCCGTCCTCTG[C/T]GATATCATTTTGTGA	63891
rs77498109	snp	C/T			downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721398	TGCCCTTCTCCTGTA[C/T]CCCACACCACCACAT	63891
rs77599182	snp	A/G	0.00925307	0.0673863	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720630	TGCCAGCCCCTGACC[A/G]GAAGCGCTTCTCCCT	63891
rs77751846	snp	A/C	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49712215	TGGGTGACTCCATCT[A/C]AAAAAAAAAAAAAAC	63891
rs77858057	snp	A/G	0.0107246	0.0724382	intron-variant	RNF123	GRCh38.p7	3:49708714	GTTCATTCGTGTTAT[A/G]GCATGTGTCAGAATT	63891
rs78079533	snp	C/T	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717845	CAGGAAGCTGGGGGG[C/T]CAGGCACAGTGCTTC	63891
rs78115322	snp	C/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696944	GGCCACCACACCCGG[C/T]CTGGACTGGTTATAC	63891
rs78221771	snp	G/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49693050	AGTTTTTTTTTTTTT[G/T]AAAAATTTTTTTTTT	63891
rs78230571	snp	A/G	0.0176615	0.0922974	intron-variant	RNF123	GRCh38.p7	3:49714067	TGTCCCATTGACCTG[A/G]GCACTGACCCCCACC	63891
rs78703149	snp	G/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696660	TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTA	63891
rs78949214	snp	C/T	0.0228947	0.104514	intron-variant	RNF123	GRCh38.p7	3:49707230	GGGGCTCTGCAGTCT[C/T]TCCCGGAGGCACACT	63891
rs79102949	snp	A/G	0.0225045	0.103662	intron-variant	RNF123	GRCh38.p7	3:49703236	GCTCTGACCTGAAAT[A/G]GCAGGGGTGGAGAAG	63891
rs79329509	snp	A/G	0.00227591	0.0336567	intron-variant	RNF123	GRCh38.p7	3:49701936	CTTGGGCACGGGGTA[A/G]GGTGGGAGGTGTGTG	63891
rs79581555	snp	A/G	0.0240643	0.107019	intron-variant	RNF123	GRCh38.p7	3:49701383	CATGCCCCTGTGGTG[A/G]TGGGAGAGCTGTGGT	63891
rs79587292	snp	C/T	0.00956631	0.0684956	intron-variant	RNF123	GRCh38.p7	3:49698836	CTGTGAGTTTCCTAT[C/T]TCTATGCACAGGCCT	63891
rs79636656	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688198	ATGAAGCTTGCCCCA[C/T]CTCATCTCTCAAATG	63891
rs79992627	snp	A/G	0	0	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688382	CATCTGTGTGGTCCT[A/G]ACACTGCTTCAGTGC	63891
rs80131850	snp	C/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49707915	CCTCTCATCTCTCTG[C/T]CTTTTTTTAGTTATG	63891
rs80300762	in-del	-/TT			intron-variant	RNF123	GRCh38.p7	3:49695280	GCTAATTTTTTTTTT[-/TT]AAGAGACAGGGTCTT	63891
rs111339391	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49706685	GGAGCCCAATCCCTT[G/T]CCTGCTCCAGGCACT	63891
rs111400749	snp	A/G	0.0134861	0.0810011	intron-variant	RNF123	GRCh38.p7	3:49701755	TGTTCTGAGTGAAGG[A/G]GGCCTGGCTAGGTCC	63891
rs111602126	snp	C/T	0.0123036	0.0774623	intron-variant	RNF123	GRCh38.p7	3:49702025	TGGTGGAGCCCTGGC[C/T]CAAACCTGCCCCCCA	63891
rs111652965	snp	C/T	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49712297	CCTCCAGGCTGAGTG[C/T]GTCCCTCTTGCCTGC	63891
rs111918004	snp	C/T	0.0134861	0.0810011	intron-variant	RNF123	GRCh38.p7	3:49713165	TGTCAGGCCCCTAGC[C/T]TGCCCCCTGCCCAGC	63891
rs111942345	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49696632	ATGAGCCACCGCACC[C/T]GGCCACATACTTTTT	63891
rs111954367	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49697556	CTACTCATCTGATGG[A/G]GCTGCAGCCAAAACT	63891
rs111964069	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49704825	ATGGGCAGGGGTCTC[A/G]TCCAGGGCCACTTCC	63891
rs112017743	snp	C/T	0.0437281	0.141251	intron-variant	RNF123	GRCh38.p7	3:49709137	TTTTTGTGATTTTTT[C/T]TTTCTTTTTTTGAGG	63891
rs112159749	snp	C/T	0.0471551	0.14613	intron-variant	RNF123	GRCh38.p7	3:49694196	GTTCTTTTCTTAAAA[C/T]GTTTTTATTGAGCTA	63891
rs112176340	snp	C/T	0.0839998	0.186933	intron-variant	RNF123	GRCh38.p7	3:49706263	TAGGTGCCCCCCACC[C/T]CCTGGGCCCAATAAG	63891
rs112178147	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690195	CTAAGGCAGTGCTGC[A/G]GAGCGAAACTCTAGA	63891
rs112205092	snp	C/T	0	0	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716759	TGGGAGGCAGGACTC[C/T]GGAGGGTGTGCCGTC	63891
rs112475134	snp	A/G	1.72982e-05	0.00294088	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49703506	GGGGGGCCTCCTCTC[A/G]CACCTGCGGAAGACC	63891
rs112479874	snp	C/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696940	CATGGGCCACCACAC[C/G]CGGCCTGGACTGGTT	63891
rs112497172	snp	A/G	0.00318978	0.0398085	intron-variant	RNF123	GRCh38.p7	3:49700837	CCAGAGCTGCCCAAC[A/G]TGGCATTTTCTCTAC	63891
rs112572467	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720455	TGGCAATCCCAAGAG[A/G]GACTTTTAGCCAGGC	63891
rs112665180	snp	C/T	0.0185938	0.0946107	intron-variant	RNF123	GRCh38.p7	3:49710382	CCTCCCAGGTTCAAG[C/T]GATTCTTCCACCTCG	63891
rs112666024	snp	C/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49702628	TTCATGCCTGGTGTC[C/T]ACAGAACATGCCCAT	63891
rs112792847	snp	A/G	0.5	0	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713952	GGCGCCCTATGAGCA[A/G]CGGCCCTGGGCCCAG	63891
rs112848517	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696372	TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC	63891
rs112875354	snp	C/T	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49706777	GATTGTCCTCCTTTC[C/T]CCTTGGGTGGCAGAG	63891
rs112921749	snp	A/G	0.0551013	0.156571	intron-variant	RNF123	GRCh38.p7	3:49700812	GGGTCCCCTGGGAGC[A/G]TCAGGAGGACCAGAG	63891
rs112961152	snp	A/C	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49713602	GGTGAGGGGCCCCTA[A/C]AGAGGGTACAGGGGG	63891
rs113355022	snp	A/G	0.00118909	0.0243543	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687821	CTCCTGCCAAGGCCC[A/G]GGCACCACCGCATGT	63891
rs113355417	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49697738	GATACAAGCCTACCC[A/G]CTCCCACCGTCCTCA	63891
rs113390708	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49715137	CAAGGCCAGGCCAAG[A/G]GCAGCAGAGGACAGT	63891
rs113391621	in-del	-/A	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49712216	GGGTGACTCCATCTC[-/A]AAAAAAAAAAAAACT	63891
rs113477650	snp	A/G	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689185	TGTCATCCCAGGGAA[A/G]GTGAGCGAGGCTGTC	63891
rs113519872	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689699	GGGCACCTGCAGCGC[A/C]GGGATCTGGGTGCGA	63891
rs113546781	snp	C/G	0.0123036	0.0774623	intron-variant	RNF123	GRCh38.p7	3:49704567	CCTGCCCAGTGTGCT[C/G]GGCTCTCTCACCGTC	63891
rs113657583	snp	C/T	3.29538e-05	0.00405904	intron-variant	RNF123	GRCh38.p7	3:49700591	TACCCCTGCCCTGAG[C/T]CCCCTGGGACTCGCC	63891
rs113690780	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49696573	TGAACTACTGACCTC[A/G]TGATCTGCCCGCCTC	63891
rs113730703	snp	A/G/T	0	0	splice-acceptor-variant	RNF123	GRCh38.p7	3:49702631	ATGCCTGGTGTCCAC[A/G/T]GAACATGCCCATGCT	63891
rs113732946	snp	A/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49714224	CAGGCGGGGGCGCTT[A/G]CCTCCTACCCATGGG	63891
rs113762151	snp	C/G	0.5	0	intron-variant	RNF123	GRCh38.p7	3:49708665	CATACACTATTTGTT[C/G]TTTTGTGTATGGCTT	63891
rs113893148	snp	A/G	0.00200142	0.0315706	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687907	GCTGCCCTGCAGAGT[A/G]GGCATGAGTGGGTGC	63891
rs113941099	snp	C/T	0	0	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688885	GTTTGGTGGGGACAC[C/T]TGAGGTGCCCTGGGG	63891
rs114148721	snp	C/G	0.00100847	0.0224325	intron-variant	RNF123	GRCh38.p7	3:49697252	CTGGAGTGGGGTTGG[C/G]AGGTGCAGAGCTGGG	63891
rs114429531	snp	C/T	0.0803703	0.183646	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687588	TCACAGCGCCCAGAA[C/T]GCCGCAGCCTCGTGT	63891
rs114810238	snp	C/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714749	CAGCAAGGACTTTCC[C/G]CTAGGCCTGGCCCTT	63891
rs114836451	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721684	AGTCCAGGGTCTTCT[A/G]ATGTGTCAGGCCAGC	63891
rs115147086	snp	C/T	0.00835141	0.0640778	intron-variant	RNF123	GRCh38.p7	3:49694628	GAGGCACGGTTGTCC[C/T]TGTCTCTCACCCCCT	63891
rs115193604	snp	A/G	0.0174175	0.0916809	intron-variant	RNF123	GRCh38.p7	3:49708198	CAAACTCCTGGCCTC[A/G]TGTGATCCTGCCACC	63891
rs115380029	snp	A/G	0.0248432	0.108648	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720391	GGGAAGCAGGGAGAC[A/G]GAAAGGATGCAGGGG	63891
rs115455998	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690269	TACCTTTGTGCTGTC[C/T]AACAGAGTAACCATT	63891
rs115601674	snp	A/G	0.00318978	0.0398085	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716831	CGGAGGACCGCCATT[A/G]TCTGCAAAGGCTCTA	63891
rs115716820	snp	C/G	0.0260105	0.111035	intron-variant	RNF123	GRCh38.p7	3:49695663	GGGTGCTTGTCCAAC[C/G]TTTGTCCCCTTCCAG	63891
rs115720876	snp	A/G	3.37388e-05	0.0041071	intron-variant	RNF123	GRCh38.p7	3:49715536	GCAGAGGCCACTGCA[A/G]TGGAGTCCCTGATGA	63891
rs116643069	snp	C/T	0.0170251	0.090679	intron-variant	RNF123	GRCh38.p7	3:49706279	CCTGGGCCCAATAAG[C/T]GCTGAAGCACACCCA	63891
rs116834078	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714748	CCAGCAAGGACTTTC[C/T]CCTAGGCCTGGCCCT	63891
rs117758999	snp	A/G	0.00020394	0.010096	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713818	GTGGAGCGAATCCCC[A/G]AGGAGCAGTGAGTGG	63891
rs137904674	snp	A/G	0.000171365	0.0092549	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713744	TCCCCGCAGACATCC[A/G]AGACTCACTGATGCA	63891
rs137961367	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49712247	TGCTTACAAATATGC[C/T]GACCAGAGTTCTGGC	63891
rs138039032	snp	C/G	0.000360116	0.0134137	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718232	GGCAGCGGCAGGCAC[C/G]GCGGCAGCAGCGGCA	63891
rs138066462	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717528	TTGAGCACCACTCCT[C/T]GAGAGCTGTCTCAGC	63891
rs138168709	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689747	GGTCTGGCAGGTCCT[C/G]TGGAGCTTGGGGCCA	63891
rs138276149	snp	C/G	3.3745e-05	0.00410748	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718280	AGAGCAGCACGAGCA[C/G]AAGGCCCACGGCACA	63891
rs138311957	snp	A/G	8.25253e-05	0.00642307	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700311	ACACAGGCACAGTCC[A/G]TGGTGCACCAGGTCC	63891
rs138335505	snp	G/T	0.000132646	0.00814281	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718940	TCAGACCGTGCAGGT[G/T]GTCGAAGGAGAACGA	63891
rs138420075	snp	C/T	0.000527478	0.0162315	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699025	GAACCTGTCCAGGGG[C/T]CTGGGTATGGCCTAC	63891
rs138522949	snp	A/G	0.000556713	0.0166747	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49703491	TGACCTGCAGCGCCT[A/G]GGGGGCCTCCTCTCG	63891
rs138638527	snp	A/G	0.0142736	0.0832652	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689668	TCCCTTCGCGGTCCG[A/G]GCTAGTCCAGTGCGA	63891
rs138638683	in-del	-/ACA	0.481242	0.0950111	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720159	GTCTCTACTAAAAAT[-/ACA]ACAACAATTAGCCGG	63891
rs138710044	snp	G/T	0.00110105	0.0234374	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687365	GGTGTTTGTCTCACT[G/T]GTGATCATTTGGGAA	63891
rs138809316	snp	A/C/T	8.43482e-05	0.00649368	intron-variant, synonymous-codon, missense	RNF123, AMIGO3	GRCh38.p7	3:49718515	TGGCGCCCTGAGAAG[A/C/T]TCCTGCTGCGGCGAA	63891
rs138880499	snp	A/C	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49692032	GTAGATTGCTTGAGT[A/C]CAGGAGTTCAAGACC	63891
rs138920124	snp	A/G	9.99534e-05	0.00706871	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691175	TGAAGGATGGCATCC[A/G]AGGGGGCCGGCATGT	63891
rs139031213	snp	C/G	0.000215526	0.0103787	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718943	GACCGTGCAGGTGGT[C/G]GAAGGAGAACGAGGC	63891
rs139041816	snp	A/G	6.67958e-05	0.00577871	synonymous-codon, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721805	TAGACTTGTGGGGCA[A/G]CACGCTGGCTCCGTT	63891
rs139314219	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49689856	CCGGATACCCCGGCG[A/G]GGTTGGACGGGATAG	63891
rs139429214	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691010	ATTCCCCTGCCCTAT[A/G]TGTTAGTGTGCATGC	63891
rs139489151	snp	A/G	8.34843e-05	0.00646028	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719325	CAGCCCTAGGCCAGT[A/G]CAGCTTAGCAGGTCG	63891
rs139508388	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49710158	CTTTTTTAATAGTAA[A/G]TCCTAATGGGTAGGA	63891
rs139572865	snp	A/T	0.00755907	0.0610114	intron-variant	RNF123	GRCh38.p7	3:49714321	GTGTCCCCTGGGGTT[A/T]CCACTTTCCCTGCTT	63891
rs139665550	snp	C/T	3.4239e-05	0.00413743	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720635	GCCCCTGACCGGAAG[C/T]GCTTCTCCCTGCAGA	63891
rs139665652	snp	A/C/T	3.54197e-05	0.00420819	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687887	GAAGTCATTCAATGG[A/C/T]GAGCGCTGCCCTGCA	63891
rs139727863	snp	A/G	1.67086e-05	0.00289033	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719186	CATCTAGTTCGTTGT[A/G]GTCTAGGTGCAGGGC	63891
rs139814207	snp	G/T	0.000447839	0.0149572	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701516	CTCCGCTCCGTCGTC[G/T]TCTTTTACATCAAGA	63891
rs139815989	snp	C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49709728	ACAGGCGTGAGCCAT[C/T]GCGCCCTGCAATTTT	63891
rs140019398	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720079	CCAGCACTTTGGGAA[A/G]CCAAGGCAGGTGGAT	63891
rs140027250	snp	A/G	0.00188685	0.0306572	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718048	AGATCGAATTCCTCA[A/G]CTACTGCCAGCTGCA	63891
rs140057242	snp	C/T	0.000248133	0.0111357	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713964	GCAGCGGCCCTGGGC[C/T]CAGACCAACTGGATC	63891
rs140195661	snp	A/G	0.00398564	0.0444627	intron-variant	RNF123	GRCh38.p7	3:49714924	AGCAAGTCCTTGCCA[A/G]TTGCCGTGGTCCTGC	63891
rs140243208	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49711928	TTCACACACCTTGTA[C/T]TCCACTTTTCCACAC	63891
rs140316856	in-del	-/CCC/CCCC			intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717602	GGCTGTAGAAGAACA[-/CCC/CCCC]CAGCCACTTCCACAG	63891
rs140583719	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698065	AGGGAAATGGCTCTA[C/T]GAGGTCCTCATCTCC	63891
rs140587538	snp	C/T	0.00241749	0.0346829	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701843	GATGAAGGAGGAGAC[C/T]GCAGAGGAGCGGCTG	63891
rs140652730	snp	C/T	6.59924e-05	0.00574385	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698487	CTATGATGGCAACCG[C/T]GTGCGCAAGTGGAAT	63891
rs140696690	snp	C/T	4.99122e-05	0.00499536	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719403	GAAACCCTCGGAGTC[C/T]GGGGTGCCTAACCCA	63891
rs140746667	snp	C/T	0.0422008	0.138995	intron-variant	RNF123	GRCh38.p7	3:49696771	CCTGCCTCTGTCTCC[C/T]GAGTAGCTGGGATTA	63891
rs140760030	snp	C/T			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699072	TCTCTTTCAAGGAGT[C/T]CGTGGCCTTCAACTT	63891
rs140793082	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690321	TCTTGAAATGTGGCT[A/G]AGGCAACTGAGAAAT	63891
rs140939614	snp	C/T	0.0119091	0.0762411	intron-variant	RNF123	GRCh38.p7	3:49696992	AATTCGGCCTTCTGA[C/T]CTCCTGCATGCCAGA	63891
rs140994707	snp	C/T	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49706877	CCGTCTTGCCTGGGT[C/T]CATGCCACTGTCTAC	63891
rs141067038	snp	A/G	3.37587e-05	0.00410831	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718823	GGTTGTTGTGCAAGT[A/G]GAGGCCGTTCTTGAG	63891
rs141089085	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49694852	ACCAGAGATGGTCCT[A/G]CTGCTGCTGCTGCTG	63891
rs141098453	snp	A/G	0.000256553	0.011323	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718696	CGCACGCGGGACGCG[A/G]GTACCTTGAAGGCCA	63891
rs141133735	snp	C/G	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690421	CACCGCTACACATCA[C/G]TGAGGCCAGCACCAG	63891
rs141168573	snp	A/G	0.00478085	0.0486577	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718223	GCCAGCGGCGGCAGC[A/G]GCAGGCACGGCGGCA	63891
rs141355511	snp	A/G	5.10747e-05	0.00505319	intron-variant	RNF123	GRCh38.p7	3:49705712	CCCGCATTGGGTGGC[A/G]GGTGTTGTGCGTGTT	63891
rs141392638	snp	C/T	0.00113744	0.0238207	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720462	CCCAAGAGAGACTTT[C/T]AGCCAGGCCCCAAGC	63891
rs141398423	snp	A/G	0.0236746	0.106192	intron-variant	RNF123	GRCh38.p7	3:49710570	CAGGCTTCAGCAACC[A/G]CGCCTGGCCATATCC	63891
rs141435306	snp	C/T	0.00210145	0.0323467	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698802	GATTGACCTGGATGA[C/T]GGCACTCTGTCCTTC	63891
rs141491956	snp	A/G	0.00812554	0.0632198	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716344	AGGCCTGGAGCCCTT[A/G]AAGCAGGAGCATGTG	63891
rs141522050	snp	A/G	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49696506	GGCACATGCCACCGC[A/G]CCCAGCATTTTTAGT	63891
rs141658855	snp	A/G	5.02955e-05	0.0050145	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705591	CCCCCGAGGAGCCTG[A/G]GCAGCCCCTCACCGA	63891
rs141686006	snp	G/T			intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716605	TCAGGTTTTGAGGCA[G/T]AGGGAAGGTGGTGAG	63891
rs141735766	snp	C/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689772	GGGCCAGGCGGGGGC[C/G]ACTTGGGGGAGCCAT	63891
rs141881740	snp	C/T			intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688515	GAGCCTCTGGCTCCC[C/T]GACTTTTTTCTCATC	63891
rs142024139	snp	A/G	0.0029652	0.0383902	intron-variant	RNF123	GRCh38.p7	3:49715535	GGCAGAGGCCACTGC[A/G]GTGGAGTCCCTGATG	63891
rs142279352	snp	A/G	0.000959539	0.0218826	intron-variant	RNF123	GRCh38.p7	3:49704770	AGGTGCCGCAGTGGG[A/G]GCAGGCGGTGGGATT	63891
rs142334123	snp	C/T	0.000219509	0.0104741	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705146	GAGAAAGTGAAGGTC[C/T]GCACGCTGAGCGTGG	63891
rs142358513	snp	A/G	0.000234813	0.0108329	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687831	GGCCCGGGCACCACC[A/G]CATGTAGCAGGTGCT	63891
rs142417750	snp	C/T	6.64253e-05	0.00576266	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701567	GCCGGCCTGCAGGAG[C/T]TCATTCCCACCACCT	63891
rs142524923	snp	C/T	0.000167205	0.0091419	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699487	CCAGTGGCAGGCTAC[C/T]GGCCCCTGCAGGACC	63891
rs142656174	snp	A/G	0.0154538	0.0865337	intron-variant	RNF123	GRCh38.p7	3:49696688	TTACTCTTGTTGCCC[A/G]GGCTGAAGTACAATG	63891
rs142786034	snp	A/C	0.00199481	0.0315187	intron-variant	RNF123	GRCh38.p7	3:49714529	CTAGCTCCCTGACCT[A/C]CAGCCTTGTCCCAGC	63891
rs142815730	snp	A/G	0.0528381	0.153711	intron-variant	RNF123	GRCh38.p7	3:49709462	CCTGCCACCACGCCC[A/G]GCTAATTTTTTGTAT	63891
rs142819877	snp	C/T	8.31774e-05	0.00644839	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719133	TAGATCGAGCAGCCT[C/T]AGGCCGCTGGCGTTG	63891
rs142839075	snp	C/G	0.00358779	0.0422022	intron-variant, utr-variant-5-prime	RNF123, AMIGO3	GRCh38.p7	3:49719653	GGTGCGGCACTCTTA[C/G]CCGCGCTCCCTTCGG	63891
rs142964215	snp	A/T	0.282742	0.247847	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687601	AACGCCGCAGCCTCG[A/T]GTGGGGCGAGTGTTG	63891
rs143071861	snp	C/T	0.00198811	0.0314659	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713790	CGTGTGCTACCCACA[C/T]TCCCTGCGGGCTGTG	63891
rs143082669	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49697181	TGCCAGAACATTTGG[A/T]CCAGTTGCTACAGGT	63891
rs143218268	snp	C/T	0.000278459	0.0117963	synonymous-codon, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721770	CATGATGATACGAGG[C/T]TCTGGCACTGACTCG	63891
rs143394687	snp	A/G	0.00184359	0.0303051	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698766	GCAGGCGTGGGCAGC[A/G]GGGGACATCGTGAGC	63891
rs143460206	snp	C/T	0.00517822	0.0506191	intron-variant	RNF123	GRCh38.p7	3:49707659	GCATGACTGGGTGAT[C/T]GAGGCCTTTGGTATC	63891
rs143613334	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49690983	CCTGTGTAGGAAGCT[A/G]GGAGCCCCTGCATTC	63891
rs143695343	snp	A/G/T	3.31347e-05	0.00407019	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718057	TCCTCAGCTACTGCC[A/G/T]GCTGCACGCGGCCAT	63891
rs143707867	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49703099	AGTCCCCAAGGGTCA[G/T]TGGGAGCCTTACCTG	63891
rs143814901	snp	G/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49710607	TTTGCTGAATTTATT[G/T]ATTAATCCTAGTTGG	63891
rs144031061	snp	C/T	3.295e-05	0.00405881	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49706023	TGAATACGCTATGGC[C/T]CTGAGGGACACAGAG	63891
rs144040971	snp	C/T	0.000116024	0.00761567	missense, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49722029	GAATGGGAACGGATC[C/T]GGGCATCCCGCAGCA	63891
rs144189297	snp	C/T	1.64773e-05	0.00287026	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720803	ACCACTCCCCAGATG[C/T]GGATTATATCAGTGC	63891
rs144203279	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49691651	TGGCTGCGAGATCTC[C/T]GGCCAGAGAGTCTGC	63891
rs144274763	snp	C/T	0.00194637	0.0311352	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687830	AGGCCCGGGCACCAC[C/T]GCATGTAGCAGGTGC	63891
rs144365800	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49704065	CCTGCCAGAGGTTGT[G/T]TGGATGGGGTGCCAT	63891
rs144421130	snp	A/G	0.00077921	0.019723	missense, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721979	CCCACTGACCCACGC[A/G]GCAGCGCCAGCCCAC	63891
rs144506153	snp	C/G/T	5.13636e-05	0.0050675	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718685	GCTGGAAGAAGCGCA[C/G/T]GCGGGACGCGGGTAC	63891
rs144519280	snp	C/T	0.000153988	0.00877328	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718191	GCTCAGCTCTTGGAG[C/T]GGGCTGGGTGTTTGG	63891
rs144665985	snp	C/T	0.00318978	0.0398085	intron-variant	RNF123	GRCh38.p7	3:49700863	TCTACAGAGCAAGGA[C/T]GAGAGAGCAAAGGAC	63891
rs144744963	snp	A/G	3.29734e-05	0.00406025	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712572	TTTGCCTTCATGCCC[A/G]AGTTCTACCTGAGCG	63891
rs144756619	snp	C/T	0.00011969	0.00773502	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49697415	CCTGGACCACACAGG[C/T]GGCTTTGAGGGGCTT	63891
rs144900603	snp	C/T	3.41898e-05	0.00413446	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718702	CGGGACGCGGGTACC[C/T]TGAAGGCCAAGCATA	63891
rs145084266	snp	A/G	5.25426e-05	0.00512529	intron-variant	RNF123	GRCh38.p7	3:49705730	TGTTGTGCGTGTTTG[A/G]TTGTGTGTGTATTCC	63891
rs145107385	snp	C/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49692522	AGTTATTTTTAAATG[C/T]ACAATTATTATTTAC	63891
rs145265101	snp	C/G	0.00211327	0.0324372	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49697427	AGGCGGCTTTGAGGG[C/G]CTTCTCCTGGTGGAT	63891
rs145300894	snp	A/G	0.000307953	0.0124049	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687580	GGAAGAGGTCACAGC[A/G]CCCAGAACGCCGCAG	63891
rs145301034	snp	A/G	0.000250482	0.0111883	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719323	TGCAGCCCTAGGCCA[A/G]TGCAGCTTAGCAGGT	63891
rs145313760	in-del	-/G			frameshift-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49705008	AGGCCCTGGCTGTTG[-/G]GGGGGCCACTGCCCC	63891
rs145379690	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691109	CTGGCCCTGAGTAGA[C/T]AGGCTCTGTGTCTGG	63891
rs145408661	snp	A/G	0.0463947	0.145069	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688426	CTAATAGAGGCCTAA[A/G]TGGGCAATGTCTATG	63891
rs145452881	snp	C/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49693693	CCTCCAAACTGTTCT[C/T]GATAGTGATTGCACT	63891
rs145532818	snp	C/T	0.000116607	0.0076348	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719345	TTAGCAGGTCGGCAG[C/T]GCAGATACATTTGTA	63891
rs145575614	snp	A/C/T	0.000132695	0.00814441	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687579	TGGAAGAGGTCACAG[A/C/T]GCCCAGAACGCCGCA	63891
rs145678564	snp	C/T	1.65162e-05	0.00287365	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712528	TCTGCCTGCGGACCA[C/T]TGAGCACGGTGATCG	63891
rs145736690	snp	G/T	0.00199481	0.0315187	intron-variant	RNF123	GRCh38.p7	3:49713013	AAAGCGTAGCAGTTG[G/T]TCAGGGGCAGAATGG	63891
rs145802061	snp	C/T	4.95479e-05	0.0049771	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49715972	TTCCTTGACTGGACC[C/T]GGCCTACCTCTGAGA	63891
rs145834474	snp	A/C/G	0.00576922	0.0533996	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699474	CTCTGGCACCTACCC[A/C/G]GTGGCAGGCTACCGG	63891
rs145834718	snp	C/G	0.00716266	0.059414	intron-variant	RNF123	GRCh38.p7	3:49715356	TCAGGGCTGGACACA[C/G]CTGCAGCCTGGGGCT	63891
rs145875764	snp	C/T	0.00233623	0.0340978	intron-variant	RNF123	GRCh38.p7	3:49699123	ATCATTTTGTGAAGA[C/T]GGCTGTGGGCTGCTC	63891
rs145883512	snp	A/G	0.00858099	0.0649374	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691437	CAGGCATTGTGCAGG[A/G]GAAGCTGCTGAATGA	63891
rs146050098	snp	C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49714917	GTCACACAGCAAGTC[C/T]TTGCCAATTGCCGTG	63891
rs146075461	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RNF123, AMIGO3	GRCh38.p7	3:49719708	TTCCTGATCGGCTCC[C/T]AAATACTCCCCCCAG	63891
rs146225272	snp	C/G/T	0.00142576	0.0266621	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701540	ATCAAGAGCCCCCTG[C/G/T]GTGTGGAGGAGGCCG	63891
rs146292595	snp	C/G/T	8.33832e-05	0.00645643	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687241	TCGCCATCAGGGTTA[C/G/T]GGCAGAAGTTCTCTT	63891
rs146532174	snp	C/T	9.88321e-05	0.00702896	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702699	CTGATCTCTGCCCTG[C/T]GCTACTATTGGGATG	63891
rs146552927	snp	C/T	4.96364e-05	0.00498154	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713958	CTATGAGCAGCGGCC[C/T]TGGGCCCAGACCAAC	63891
rs146592630	snp	C/T	4.97426e-05	0.00498686	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699681	AGGAGGGGCGGCTGT[C/T]GGACAAGGAGAGCTC	63891
rs146610954	snp	A/G	1.64988e-05	0.00287213	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698490	TGATGGCAACCGCGT[A/G]CGCAAGTGGAATGTG	63891
rs146619038	snp	A/G	0.000315471	0.0125553	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705613	CCTCACCGAGAACTC[A/G]CTGCTGGAAGTCCTG	63891
rs146637200	snp	C/T	0.00557542	0.0525036	intron-variant	RNF123	GRCh38.p7	3:49710569	ACAGGCTTCAGCAAC[C/T]GCGCCTGGCCATATC	63891
rs146712306	snp	A/G	4.96192e-05	0.00498067	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713987	ACTGGATCCTGGTGC[A/G]GCTCTGGAGGGTAAG	63891
rs146833478	snp	A/G	3.29451e-05	0.00405851	downstream-variant-500B, missense, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721252	ACCACCATCGTGTCT[A/G]TAGAGGACTGGGAGA	63891
rs146969257	snp	A/G	1.67885e-05	0.00289724	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49716124	ACCAGGTGCTGAACC[A/G]GGTGACAGCTGAGAG	63891
rs147074020	snp	A/G	0.000497422	0.0157627	synonymous-codon, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721818	CAGCACGCTGGCTCC[A/G]TTGAGGTAGAGCTCA	63891
rs147272863	snp	C/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49704462	TGAGTGGCAGCTAGA[C/T]GGGGCCCTTGAGATG	63891
rs147517381	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49693549	TTTAGTAGAGATGGG[A/G]TTTCGCCATGTTGGC	63891
rs147594041	snp	C/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49715501	CCAAAGCCTCAATGG[C/G]CGAGGACAGAGGCAA	63891
rs147651287	snp	A/G	7.16397e-05	0.00598454	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687892	CATTCAATGGCGAGC[A/G]CTGCCCTGCAGAGTA	63891
rs147714661	snp	A/G	0.000265358	0.0115156	synonymous-codon, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721977	TACCCACTGACCCAC[A/G]CGGCAGCGCCAGCCC	63891
rs147766469	snp	C/T	0.0029345	0.0381921	intron-variant	RNF123	GRCh38.p7	3:49716084	CCATCCACCAATGGA[C/T]TCCTGCTCCCCTCAC	63891
rs147980322	snp	A/G	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49707684	GGTATCCCCATTTCT[A/G]TCATCTCTGCTTGCT	63891
rs147997200	snp	A/G	0.0759472	0.179459	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688745	GCTCTGGCTCCACAC[A/G]TCAGCTCAGGGCCTG	63891
rs148034082	snp	C/T	0.00350987	0.0417447	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713797	TACCCACACTCCCTG[C/T]GGGCTGTGGAGCGAA	63891
rs148158961	snp	A/G	0.00256761	0.0357381	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49717972	TGTCATGGGACCCTC[A/G]GAGCCTATGGAGCTG	63891
rs148209804	snp	G/T	0.0236746	0.106192	intron-variant	RNF123	GRCh38.p7	3:49701121	GGCTGGGAAGCCTCA[G/T]CTTGTAGCCGTTTTC	63891
rs148561345	snp	C/G/T	3.43377e-05	0.00414339	missense, synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49704717	AACCGCCATGGATGA[C/G/T]CTAGATGAGGATGAG	63891
rs148608408	snp	A/G	6.59055e-05	0.00574007	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720804	CCACTCCCCAGATGC[A/G]GATTATATCAGTGCC	63891
rs148678579	snp	A/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688035	TATGCACTTTCAAGG[A/G]CCAGTCTAGCCCCCT	63891
rs148735642	snp	C/T	0.000151584	0.00870454	intron-variant	RNF123	GRCh38.p7	3:49704609	CACTGTGGCCCCTTG[C/T]GCCACCACTGGCCTG	63891
rs148841955	snp	A/G	3.46687e-05	0.00416331	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688611	ACCAGGGACCCCTAA[A/G]CATTGAGTCAGAAGC	63891
rs148871026	snp	A/G	5.14275e-05	0.00507061	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49703433	TCCTCGCAGAGGCCT[A/G]CATCCCGCCCCAGGT	63891
rs149050592	snp	A/C	0.0134861	0.0810011	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689649	CCTGGCGGGTTCCGG[A/C]TATTCCCTTCGCGGT	63891
rs149103139	snp	C/G	0.00139604	0.0263832	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718125	CTTGTGGACGCTGGC[C/G]TTGCGGCTGGGTGCG	63891
rs149224835	in-del	-/A			intron-variant	RNF123	GRCh38.p7	3:49713209	GCAGGCTTTGTCTTC[-/A]AAGACAGAGCTGTGA	63891
rs149412652	snp	A/G	6.60753e-05	0.00574746	missense, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716404	TCAGGCCTAGAGAGC[A/G]TGGACCACTATCCCA	63891
rs149527081	snp	C/T	0.0260105	0.111035	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690728	AATGTGTAGGATTGT[C/T]GCTTCTGGTTGTGAG	63891
rs149587534	snp	C/T	3.32353e-05	0.00407634	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719103	GCGGCCAAGCGCCCG[C/T]AACGTGTTAGATGAT	63891
rs149674609	snp	A/T	0.000153988	0.00877328	splice-acceptor-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687899	TGGCGAGCGCTGCCC[A/T]GCAGAGTAGGCATGA	63891
rs149850921	snp	A/C	0.0236746	0.106192	intron-variant	RNF123	GRCh38.p7	3:49715088	ACTGCTGCCTGCCAG[A/C]CCAGACTTGGTGCCC	63891
rs149904191	snp	C/T	8.26412e-05	0.00642758	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698123	TGCACCATCAGCTGC[C/T]GCTTCAACCAGGAGG	63891
rs149909642	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49704687	CATTGTGATCGACCC[A/G]CTGGAGCTCCAGTCA	63891
rs149938600	snp	A/C	0.000153988	0.00877328	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718059	CTCAGCTACTGCCAG[A/C]TGCACGCGGCCATTG	63891
rs150039459	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721696	TCTGATGTGTCAGGC[C/T]AGCACTCCCCTTGCT	63891
rs150056608	snp	A/C			intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691049	TCACCTGCTCCCAAG[A/C]CTTCCTGCCATGGCA	63891
rs150074311	in-del	-/G			frameshift-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49699704	AGAGCTCCAAGTGGC[-/G]GGTTGCGGGGCCAGC	63891
rs150080768	snp	A/G	4.99164e-05	0.00499557	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49715612	GCAGCAGCACATGGC[A/G]GACCTCCTACAGCAG	63891
rs150180251	snp	C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49698319	AGAATACCTCTTACT[C/T]TTTCCCTCAGATCAT	63891
rs150267931	snp	A/G	4.97211e-05	0.00498579	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699688	GCGGCTGTTGGACAA[A/G]GAGAGCTCCAAGTGG	63891
rs150320753	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49712118	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG	63891
rs150374322	snp	A/G	0.0126979	0.078662	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49716909	AGGATGGCCATGGGG[A/G]CCCCCAGCTCGGCCC	63891
rs150377616	snp	A/G	1.64841e-05	0.00287085	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712632	AATTACTTTGGTCCC[A/G]TGCACAGCATGGAGG	63891
rs150478395	snp	A/T	1.764e-05	0.00296979	synonymous-codon, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721764	CCCTCACATGATGAT[A/T]CGAGGCTCTGGCACT	63891
rs150548886	snp	A/G	4.94279e-05	0.00497107	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49706003	GGTGTCTCCGATGAT[A/G]TCAATGAATACGCTA	63891
rs150551790	snp	C/G	1.69651e-05	0.00291243	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718589	GCCTCAGGGACCGAC[C/G]CACCAGCGCGTACAG	63891
rs150711622	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49702540	TGCTTTTCCCTCCCT[A/G]CTTAACCCTCGACCC	63891
rs150738623	snp	C/T	0.000141136	0.00839928	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49703513	CTCCTCTCGCACCTG[C/T]GGAAGACCCTCAAAG	63891
rs150794161	snp	C/T	1.66211e-05	0.00288275	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701509	CGACGTGCTCCGCTC[C/T]GTCGTCTTCTTTTAC	63891
rs150915433	snp	A/G	1.65853e-05	0.00287964	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713912	CTTGCCCTCACAGGC[A/G]TATCGCCATGGTGAG	63891
rs151132700	snp	C/T	0.000576925	0.0169744	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698101	GGGGCTCATGCAGAT[C/T]GGCTGGTGCACCATC	63891
rs151208351	snp	A/G	0.0244538	0.107838	intron-variant	RNF123	GRCh38.p7	3:49695757	GGCACCCTGTGGGCA[A/G]CCAGGTGTGTAATGG	63891
rs151244822	snp	C/T	3.78465e-05	0.00434992	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49704984	CTTTCTTCACTGCAG[C/T]GCCCCATGCAGGCCC	63891
rs151252055	snp	C/T	0.000281144	0.011853	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705150	AAGTGAAGGTCCGCA[C/T]GCTGAGCGTGGAGCA	63891
rs151294484	snp	A/G	0.0236746	0.106192	intron-variant	RNF123	GRCh38.p7	3:49711748	CCTGACATAGACTTT[A/G]TGGAAACCACATTGT	63891
rs180702572	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49701291	TCGTGCACCTGCTGG[A/G]TACTGGAGCTGGTGG	63891
rs180719032	snp	A/G	0.00358779	0.0422022	intron-variant	RNF123	GRCh38.p7	3:49710960	AATCCCATTATTAAT[A/G]GAGAGATTCACTCCT	63891
rs181013266	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720417	AGGGGGGGTGATCAT[A/G]TACGAGCCATGGCAC	63891
rs181052824	snp	C/T	0.000263562	0.0114766	intron-variant	RNF123	GRCh38.p7	3:49704807	GGGCTTATCCTGTAT[C/T]TTATGGGCAGGGGTC	63891
rs181075011	snp	A/C	0.0023933	0.0345097	intron-variant	RNF123	GRCh38.p7	3:49693308	CCACCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC	63891
rs181203125	snp	C/T			intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688349	GCTCAGGAGGGGTCA[C/T]TGCCTGCTGTGTGCG	63891
rs181213022	snp	A/G	0.00274826	0.0369673	intron-variant	RNF123	GRCh38.p7	3:49700458	CATGGCTGCCTTGGC[A/G]TCTCTTCCCCCAGGA	63891
rs181221894	snp	G/T	0.0138799	0.0821421	intron-variant	RNF123	GRCh38.p7	3:49713392	CAGATGCCACCCTGG[G/T]TCCAGGCTGGCCTTG	63891
rs181529239	snp	C/G/T	8.31879e-05	0.0064489	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719122	GTGTTAGATGATAGA[C/G/T]CGAGCAGCCTCAGGC	63891
rs181661411	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692669	TCCAGTACTTTGCCT[C/T]TATGAGTTCAATTGT	63891
rs181807071	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49705248	TACAGTCCCCGATCC[A/G]GGCAAAGCCAAAATA	63891
rs181910968	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49711436	ATCTCAATCCGGCCG[A/G]CACATTTCCATCTCC	63891
rs182031739	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49692219	TGCCACTGCACTGTA[A/G]CCTGGGTGACAGAGC	63891
rs182094431	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714474	TTCCTGGCCTGCTAC[A/G]GCTCATGCAGACTGA	63891
rs182125211	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689401	GAGGTCGGAGGTGGT[A/G]AGGCCTTTCGGCGAA	63891
rs182179992	snp	A/G	0.000397351	0.0140896	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687609	AGCCTCGTGTGGGGC[A/G]AGTGTTGAGTCCATG	63891
rs182273614	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49691930	TGTAGTCAGTATAAA[A/C]GTTACAAGTACATTT	63891
rs182307446	snp	C/T	0.00398564	0.0444627	intron-variant	RNF123	GRCh38.p7	3:49696203	CCTTCTTCTTCCAGA[C/T]ATCATCAGCACAGCC	63891
rs182605664	snp	C/T	0.00358779	0.0422022	intron-variant	RNF123	GRCh38.p7	3:49702499	CGGACTGCCTCATCC[C/T]TGCCTAGCCCCAAGC	63891
rs182626818	snp	C/T	0.00092333	0.0214665	intron-variant	RNF123	GRCh38.p7	3:49702801	CTGGACAGAGCCAGG[C/T]GTAGGGCAGCCCCTA	63891
rs182716766	snp	A/G	0.00755907	0.0610114	intron-variant	RNF123	GRCh38.p7	3:49695448	TGGGCCCACTGGGGT[A/G]TTCAGAGATGGGGTT	63891
rs182739180	snp	G/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49708619	TCTGTCTCTGAATTT[G/T]ACTATACTAAGCACC	63891
rs183025105	snp	A/G	3.30022e-05	0.00406202	intron-variant	RNF123	GRCh38.p7	3:49702442	CCACTGTGGATCCCC[A/G]GCTGCACTACACATG	63891
rs183478011	snp	A/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49708934	GAATTACTGTATCAT[A/T]TGGTAATTCTGTTTT	63891
rs183570498	snp	A/C	0.0023933	0.0345097	intron-variant	RNF123	GRCh38.p7	3:49714943	CCGTGGTCCTGCGTC[A/C]AGGGCGGAACTGAGC	63891
rs183609993	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691488	CCTCTTCTGAACATG[C/T]ACCCCCAGCAGCCAC	63891
rs183616173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716585	CTGGAAAATGGACCT[C/T]AGCATCAGGTTTTGA	63891
rs183795375	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49693988	GTTTGCGTTCTTTGT[A/G]TATTCTGGTTATTAA	63891
rs183827603	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689820	CTTGGGCTCCCAGAC[A/G]GAGTAGGTTCAGTTC	63891
rs184035563	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690238	AATAGAACTTTATAT[A/G]ATGGTGGGAACGTTC	63891
rs184127567	snp	C/T	0.00175869	0.0296015	missense, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721787	CTGGCACTGACTCGC[C/T]AATAGACTTGTGGGG	63891
rs184426850	snp	A/C	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49704833	GGGTCTCATCCAGGG[A/C]CACTTCCCGCTCCAT	63891
rs184454753	snp	C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49710226	TTAGTGACATTATGA[C/T]AAATAGTACCTTTAC	63891
rs184530129	snp	A/G	0.00254103	0.0355536	intron-variant	RNF123	GRCh38.p7	3:49699606	GGGTCTGGGCCAGGC[A/G]GGGTGGGGGGCTTCC	63891
rs184672885	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49703572	GTTCTGGGGCCAGGT[G/T]GGGGACTGTCCCTGA	63891
rs184741595	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49711197	AAAAATTAGCAGGGC[A/G/T]TGGTATCACATACCT	63891
rs184795905	snp	A/G	0.00358779	0.0422022	intron-variant	RNF123	GRCh38.p7	3:49704420	TAAATGAAAAAGAAG[A/G]GTGTGATGGGGAAGG	63891
rs184946730	snp	A/G	4.95299e-05	0.00497619	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49715953	CACACTGGTGCCTGA[A/G]ATATTCCTTGACTGG	63891
rs185245937	snp	C/T	1.64727e-05	0.00286986	downstream-variant-500B, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721251	AACCACCATCGTGTC[C/T]GTAGAGGACTGGGAG	63891
rs185264656	snp	C/T	0.00517822	0.0506191	intron-variant	RNF123	GRCh38.p7	3:49709772	CAGATGGGGTTTCAC[C/T]GTGTTGGTCAGGCTG	63891
rs185283000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49693663	CACCTGACCAATTTT[C/T]AGTTTTTTGAGGAAC	63891
rs185287736	snp	C/T	0.000399281	0.0141238	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718748	AGTCGCGCACGGCGC[C/T]CAGGCCCCGCTGGTG	63891
rs185394915	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49692364	AATTTTTGTGGGTAT[A/G]TAGTAGGTATATATA	63891
rs185420417	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689655	GGGTTCCGGCTATTC[C/T]CTTCGCGGTCCGGGC	63891
rs185433400	snp	C/T	0.00108681	0.0232857	intron-variant	RNF123	GRCh38.p7	3:49700630	CTGAACGCCCCCTCT[C/T]CACAGATCCATTACC	63891
rs185599246	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689251	CAGGGACTCTGGCAG[A/G]AACGGCCTTTCAGAC	63891
rs185616423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49698355	CCCTTCTGTAGAGCC[A/G]TATGCATCCAAGGCT	63891
rs185704507	snp	A/G	3.32901e-05	0.0040797	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719352	GTCGGCAGCGCAGAT[A/G]CATTTGTAGGGGCAG	63891
rs185743756	snp	A/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49692722	TAAGTGATAACATGC[A/T]ATGTTTGTCTTTTTC	63891
rs185801770	snp	C/T	0.00342662	0.0412501	intron-variant	RNF123	GRCh38.p7	3:49702447	GTGGATCCCCGGCTG[C/T]ACTACACATGCCATG	63891
rs186144778	snp	C/G/T	0.000288501	0.0120076	intron-variant	RNF123	GRCh38.p7	3:49705530	TCCCTCCCCAACTCC[C/G/T]CAGTTGAAGGCAGCC	63891
rs186251589	snp	A/T	0.000351502	0.0132524	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713791	GTGTGCTACCCACAC[A/T]CCCTGCGGGCTGTGG	63891
rs186365107	snp	C/T	0.0244538	0.107838	intron-variant	RNF123	GRCh38.p7	3:49707674	CGAGGCCTTTGGTAT[C/T]CCCATTTCTATCATC	63891
rs186715278	snp	G/T	1.65963e-05	0.0028806	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687738	TCTTATCTAGGCCCA[G/T]TGGCCACTCACCGGC	63891
rs186846417	snp	G/T	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690743	CGCTTCTGGTTGTGA[G/T]CTGGACTCAGTATGG	63891
rs186858183	snp	C/T	1.68644e-05	0.00290378	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49716163	TTGATCGTGTGGTCA[C/T]CCTACGGCTGCCTGG	63891
rs186934515	snp	G/T	0.00358779	0.0422022	intron-variant	RNF123	GRCh38.p7	3:49711646	GTGTGAAGCCCAGGT[G/T]CTGTGACCGCACTCC	63891
rs187177227	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49695724	AGAACTGGCATTAAA[A/G]GTGGAAGAGCAGGTG	63891
rs187234777	snp	C/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49694592	CTTCAAAGGATCAAG[C/T]AGGTTCTCCCTCCCT	63891
rs187714448	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49709013	CACTCTGTCACCCAG[A/G]CTGGAGTGCAATGGT	63891
rs187811282	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49708684	TGTGTATGGCTTTAG[C/T]ATAATGTCCTCAAGG	63891
rs188066975	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714796	GCCACACACTGTCCT[C/T]ACCCTTCATGGTGGC	63891
rs188115176	snp	A/G/T	3.35927e-05	0.00409822	intron-variant	RNF123	GRCh38.p7	3:49699792	GCGGCATTGGGAGGG[A/G/T]CATGGGAGGGGAGGA	63891
rs188127966	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702650	CATGCCCATGCTCTG[C/T]CCCCCTGAGTACATG	63891
rs188131188	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49709986	CATACATATCCTTAC[C/T]GACACTTCTTATTTT	63891
rs188238881	snp	C/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49710867	GATGTTAGATGGAGG[C/G]TTTTCATATATGGTC	63891
rs188322715	snp	C/T	0.0248432	0.108648	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49689945	ACTGACTCCCGGAGC[C/T]CACTCCGGGTGTCTG	63891
rs188496660	snp	C/G	0.00517822	0.0506191	intron-variant	RNF123	GRCh38.p7	3:49693119	AGGGGCACAATCTCA[C/G]CTCACTGCAAGCTCC	63891
rs188570998	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49715151	GGGCAGCAGAGGACA[A/G]TAGAGGACAGCAGGT	63891
rs188651373	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720189	GGCGTGGTGGTGGGC[A/G]TCTGCAATTCCAGCT	63891
rs188842898	snp	A/T	3.40009e-05	0.00412302	intron-variant	RNF123	GRCh38.p7	3:49699816	GGGAGGAGACAGGCC[A/T]TGCTAGACACGCCCG	63891
rs188965337	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49703072	GGTGGGTGCTGGGGG[A/G]CCCTGTGTTTGAGTC	63891
rs188997301	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49704361	CAGCAGGAAGGGCAT[A/G]ATGGGCTTACATCTA	63891
rs189135441	snp	C/T	1.65581e-05	0.00287728	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687608	CAGCCTCGTGTGGGG[C/T]GAGTGTTGAGTCCAT	63891
rs189145859	snp	G/T	0.00676609	0.0577691	intron-variant	RNF123	GRCh38.p7	3:49711319	AGTTATGCTCTCTCC[G/T]TCTTTCTCTGTCTTA	63891
rs189225350	snp	C/G	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49700789	GAAGGGGAGTGTCAT[C/G]AGGCCAGGGGTCCCC	63891
rs189455787	snp	A/G	0.00284676	0.0376202	intron-variant	RNF123	GRCh38.p7	3:49705217	AGGCAGGTCCCCGAA[A/G]GACCCTTCCACAGTG	63891
rs189486260	snp	C/T	0.0162398	0.0886349	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717469	CCCTGTGGGCCCACT[C/T]CCTCCCACCCCCTTG	63891
rs189656224	snp	A/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49704481	GCCCTTGAGATGCAG[A/T]GTGAAGGCTGGGTGG	63891
rs189910529	snp	G/T	0.0240643	0.107019	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689388	CCCAGAGCAGGCGGA[G/T]GTCGGAGGTGGTGAG	63891
rs190051026	snp	A/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689667	TTCCCTTCGCGGTCC[A/G]GGCTAGTCCAGTGCG	63891
rs190078232	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49692383	TAGGTATATATATTT[A/G]TAGGGTACATGAGAT	63891
rs190214961	snp	A/C	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49702477	GCCCTCAGCACCTGG[A/C]ACTTCTCGGACTGCC	63891
rs190335089	snp	A/G	8.30862e-05	0.00644486	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718913	GGTCCAGAGTAAGCA[A/G]GTGGGTGGCGCTCAG	63891
rs190557398	snp	C/T	9.88468e-05	0.00702948	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49706014	TGATGTCAATGAATA[C/T]GCTATGGCTCTGAGG	63891
rs190990707	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714921	CACAGCAAGTCCTTG[C/T]CAATTGCCGTGGTCC	63891
rs191157788	snp	A/G	0.00199481	0.0315187	intron-variant	RNF123	GRCh38.p7	3:49708766	AATATTCTGTTGTAC[A/G]GACACCACATTTCAT	63891
rs191284657	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691072	CCATGGCAGGACTGA[A/G]GTCAGGTGTGGGGGC	63891
rs191296119	snp	A/C/G	0.000297437	0.0121917	missense, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716402	CCTCAGGCCTAGAGA[A/C/G]CGTGGACCACTATCC	63891
rs191329875	snp	C/T	0.0023933	0.0345097	intron-variant	RNF123	GRCh38.p7	3:49713002	GCACTGGTCACAAAG[C/T]GTAGCAGTTGGTCAG	63891
rs191413135	snp	A/G	0.00716266	0.059414	intron-variant	RNF123	GRCh38.p7	3:49708248	GGGTTACAGGCGTGC[A/G]CCACTGTGCCCGGTC	63891
rs191554836	snp	A/G	8.76232e-05	0.00661845	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687883	CTTGGAAGTCATTCA[A/G]TGGCGAGCGCTGCCC	63891
rs191606042	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49694648	TCTCACCCCCTCATC[A/G]GCCTTAGCTGTTCTG	63891
rs191638724	snp	C/T	0.0252325	0.109451	intron-variant	RNF123	GRCh38.p7	3:49695937	AGATTTTTCCCAACT[C/T]CTTTGGCTCGGGTAG	63891
rs191964003	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, utr-variant-5-prime	MST1, RNF123	GRCh38.p7	3:49689723	GGTGCGAAACTCCGA[A/G]CGGAAGCTGGTCTGG	63891
rs191996618	snp	A/G	0.00036616	0.0135258	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687751	CAGTGGCCACTCACC[A/G]GCAGTCCATTAAGGG	63891
rs192049545	snp	C/T	0.00135217	0.0259665	downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721387	TGAGCTCCCTTTGCC[C/T]TTCTCCTGTATCCCA	63891
rs192053943	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49704366	GGAAGGGCATGATGG[G/T]CTTACATCTATGTAG	63891
rs192156005	snp	G/T	0.00755907	0.0610114	intron-variant	RNF123	GRCh38.p7	3:49709568	GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA	63891
rs192171818	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49699419	GCAGTGGAGAGGGAG[C/T]AGGCATGTCTGAGCC	63891
rs192270390	snp	C/T	6.59033e-05	0.00573997	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702363	GTATATCTTCCTGAC[C/T]AAGTTTCGCAAGTTT	63891
rs192360100	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702719	CTATTGGGATGAATA[C/T]AAGGCTTCCAATCCT	63891
rs192455832	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49693908	TATGTCTTCTTTTGA[A/G]AAATGTCTGTTCGTA	63891
rs192497276	snp	C/T	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49703198	CATGAGTACCCCCAT[C/T]ACCCCAAGTTATGCA	63891
rs192621468	snp	C/T	1.70831e-05	0.00292254	intron-variant	RNF123	GRCh38.p7	3:49697350	TGCCTGACCCCACCT[C/T]TCCTCTTTTCAGGAC	63891
rs192845183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49715374	GCAGCCTGGGGCTTG[C/T]CTAGTAGAAGGAGGG	63891
rs192880052	snp	A/G	0.00318978	0.0398085	intron-variant	RNF123	GRCh38.p7	3:49710132	TGAGCCACCACACCC[A/G]GCAATTTCTACTTTT	63891
rs193049564	snp	G/T			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690117	CCACAAGGGTTTGTG[G/T]CGGGAGTAGAGGGTC	63891
rs199514421	snp	C/T	0.000454236	0.0150636	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713565	CGCCAAACACTTTGC[C/T]GACGCACGCATTGTG	63891
rs199537166	snp	A/G	0.000642076	0.017906	intron-variant	RNF123	GRCh38.p7	3:49705700	GCACTCTTGGACCCC[A/G]CATTGGGTGGCGGGT	63891
rs199541925	snp	C/T	3.38822e-05	0.00411582	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720587	TATCTCCTGGGACAG[C/T]CAGAGCCCCCAGCAC	63891
rs199544911	snp	C/T	0.000417589	0.0144437	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701889	GAACGGGGCTGTCAG[C/T]GGCTCAGGAAGCGCA	63891
rs199566932	snp	A/G	1.67351e-05	0.00289263	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718394	GGTTGTGGTGCAGGC[A/G]GGGCCCAGTGGCCAG	63891
rs199572300	in-del	-/A			intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687999	GGGATCAAAGCTACA[-/A]GGCTTCTGGGATGGA	63891
rs199576148	snp	A/G	6.78012e-05	0.00582203	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705581	CTGGGGCGGCCCCCC[A/G]AGGAGCCTGAGCAGC	63891
rs199587729	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49694237	ACAATAAACTACACA[C/T]ACTTAAAGTGTACAA	63891
rs199639664	in-del	-/T			frameshift-variant, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691469	TACCTGAACCGCATC[-/T]TTTCCTCTTCTGAAC	63891
rs199664585	snp	C/T	0.000198886	0.00997013	intron-variant	RNF123	GRCh38.p7	3:49698967	TGGCTCACAGACCCA[C/T]CCTTCTCCCCAGGAA	63891
rs199670077	snp	C/G/T	0.000520309	0.0161211	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718440	CGCATGCTGCTCCTG[C/G/T]ACGTTGCCTATGGCC	63891
rs199686521	snp	C/G	1.67705e-05	0.00289568	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719260	TGGAGCGCGTTGTGG[C/G]TCAGGTCGAGGTCCG	63891
rs199763252	snp	C/T	2.53001e-05	0.0035566	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705127	GCGGCCTCTGAGCAC[C/T]TCGGAGAAAGTGAAG	63891
rs199818411	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49693158	GGTTCATGCCATTCT[C/T]CTGCCTCAGCCTCCC	63891
rs199836723	snp	A/G	4.96586e-05	0.00498265	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712512	TACTGGCTGCTGCGC[A/G]TCTGCCTGCGGACCA	63891
rs199876340	snp	C/T			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49706046	ACACAGAGGACAAGC[C/T]CCGCCGGTGCCCCAA	63891
rs199902925	snp	A/G	9.93164e-05	0.00704616	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49715661	AGCTTCCTCAACAGC[A/G]TCCTCAATCAGCTCA	63891
rs199922550	snp	C/T	0.000148749	0.00862279	GMPPB, RNF123	3	allele_origin=T(germline)/C(germline)	3:49721847	CATCATTAACTATGA[C/T]GTCCTCACCCAGCAC	63891
rs199930454	snp	C/T	4.94311e-05	0.00497123	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698070	AATGGCTCTACGAGG[C/T]CCTCATCTCCTCCCA	63891
rs199932717	snp	A/G	0.000166124	0.00911232	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699753	TGGCCCACATCTTCC[A/G]TCACTTTGCACCGCT	63891
rs199933786	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721197	TAGAGCCTGTATCAA[C/T]CAGCACCTGATGAAC	63891
rs199966236	in-del	-/A			intron-variant	RNF123	GRCh38.p7	3:49711058	GCAACCCATCTCTAC[-/A]AAAAAAAACAAAATT	63891
rs199982251	snp	C/T	0.000115379	0.00759449	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49712631	GAATTACTTTGGTCC[C/T]GTGCACAGCATGGAG	63891
rs199985742	snp	A/G			splice-donor-variant	RNF123	GRCh38.p7	3:49713826	AATCCCCGAGGAGCA[A/G]TGAGTGGGGCCTGGG	63891
rs199987645	snp	C/T	0.000632227	0.0177683	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49715611	TGCAGCAGCACATGG[C/T]GGACCTCCTACAGCA	63891
rs200056189	snp	A/G	1.65329e-05	0.0028751	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691200	GCATGTCTTTCTCCC[A/G]CAAGAGCTATAGGCT	63891
rs200065075	snp	A/G	1.71132e-05	0.00292511	intron-variant	RNF123	GRCh38.p7	3:49699598	GTGAGCTGGGGTCTG[A/G]GCCAGGCGGGGTGGG	63891
rs200083046	snp	A/G	0.000399281	0.0141238	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718808	AGTCGCAAGGCAAAG[A/G]GTTGTTGTGCAAGTA	63891
rs200083584	snp	C/T	1.77976e-05	0.00298303	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717942	CTGGGTGGGGGAGCC[C/T]TGGGCAGTCTAGGTT	63891
rs200136137	snp	C/T	0.00199792	0.0315431	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687799	ACTCTTCAGCATCTG[C/T]CACATCCTCCTGCCA	63891
rs200151379	snp	C/G	0.000399281	0.0141238	stop-gained, nc-transcript-variant	RNF123	GRCh38.p7	3:49700528	TCTGCTTCGGCTGTA[C/G]CGATTCTCACCCATT	63891
rs200170860	snp	A/C	0.000132273	0.00813136	downstream-variant-500B, intron-variant, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721115	CTGCAAGTAAGTGGG[A/C]CCCACAGCTTGGTGG	63891
rs200192424	snp	A/G			intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688000	GGATCAAAGCTACAA[A/G]GCTTCTGGGATGGAC	63891
rs200193624	snp	C/T	0.000798403	0.0199641	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719089	CCGTCGAGGTCGTGG[C/T]GGCCAAGCGCCCGCA	63891
rs200239238	snp	C/T			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702400	GAGAACGCCAGTGGC[C/T]GGGGGGTAGGTGTCC	63891
rs200240656	snp	A/G	1.6504e-05	0.00287258	missense, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716446	GTGACGGGCATCCTG[A/G]TGCAGCTCCTGGTGC	63891
rs200258927	snp	C/G	0.00333525	0.0407001	intron-variant	RNF123	GRCh38.p7	3:49704771	GGTGCCGCAGTGGGG[C/G]CAGGCGGTGGGATTT	63891
rs200266739	snp	A/G	0.000151272	0.00869558	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49719241	CCAGCCGGGGCGCAG[A/G]CGCTGGAGCGCGTTG	63891
rs200267865	snp	C/T	0.000266396	0.0115381	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701494	GACACCCGCCAGCTT[C/T]GACGTGCTCCGCTCC	63891
rs200279168	snp	A/G	0.00138418	0.0262712	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701844	ATGAAGGAGGAGACC[A/G]CAGAGGAGCGGCTGC	63891
rs200303852	snp	A/G/T	0.000265658	0.0115224	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691464	ATGACTACCTGAACC[A/G/T]CATCTTTTCCTCTTC	63891
rs200318545	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692540	AATTATTATTTACTA[C/T]AGTCACTCTGTTCTG	63891
rs200334203	snp	C/G	0.00322039	0.0399978	intron-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49712689	GCTGAGGCAGAAGCA[C/G]AAAAGGGGTCTCTAG	63891
rs200445705	snp	C/T	2.16847e-05	0.0032927	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713562	TCTCGCCAAACACTT[C/T]GCCGACGCACGCATT	63891
rs200446137	snp	A/C	3.31433e-05	0.0040707	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698821	ACTCTGTCCTTCTGC[A/C]TGTGAGTTTCCTATC	63891
rs200455167	snp	G/T	0.000302003	0.0122846	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718309	CAGCCCAGCAGTGTG[G/T]TGAAGCCTGTGTTGA	63891
rs200455397	snp	A/G			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49704667	GACCTTGCTTCCAAA[A/G]CCAACATTGTGATCG	63891
rs200497573	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49704783	GGGGCAGGCGGTGGG[C/T]TTTGTGTTGGGCTTA	63891
rs200529859	in-del	-/T			intron-variant	RNF123	GRCh38.p7	3:49692317	TGTGATTCTTTTCTG[-/T]TTTCTTTCTTTGTGT	63891
rs200547779	snp	C/G	1.64863e-05	0.00287104	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702403	AACGCCAGTGGCCGG[C/G]GGGTAGGTGTCCTCC	63891
rs200572214	snp	A/G	0.00199794	0.0315433	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718615	TACAGGTGCTCTTCC[A/G]GCCGCTCTAGGCCAA	63891
rs200586465	snp	C/T	0.000409417	0.0143018	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701853	GAGACCGCAGAGGAG[C/T]GGCTGCGGCGGCGAG	63891
rs200597948	snp	A/C	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720543	CAGTGCTCCTGGCAG[A/C]TCCCTGCTTCCAGCT	63891
rs200618925	snp	G/T	0.00199808	0.0315444	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705984	CCATGCTGTGTAGAT[G/T]GTGGGTGTCTCCGAT	63891
rs200716053	snp	A/G	0.00199798	0.0315436	intron-variant	RNF123	GRCh38.p7	3:49700223	GTGCCTGGCCTTGGT[A/G]CAGCGCAAGGTGTAT	63891
rs200779427	snp	A/C/G	0.00359989	0.0422727	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716370	ATGTGGGTGGCTCAT[A/C/G]TCTTTCCTCCCCTTC	63891
rs200802665	snp	A/G	0.000280289	0.0118349	intron-variant	RNF123	GRCh38.p7	3:49699446	AGCCACAGATAAGGC[A/G]TTGCTGGCTTAACTC	63891
rs200815465	snp	C/T	0.000283757	0.0119079	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687553	CTCTCCACCCCCACT[C/T]GCCTTTCTTCTGGAA	63891
rs200829190	snp	C/T	0.000313591	0.0125179	intron-variant	RNF123	GRCh38.p7	3:49714087	TGACCCCCACCTCCA[C/T]AGGGCTGTGGCTTCG	63891
rs200842697	snp	C/G			intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688065	TGCACAGATACTTGT[C/G]AAAAAAATTTCCCCT	63891
rs200850505	snp	A/G			missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691209	TCTCCCGCAAGAGCT[A/G]TAGGCTGACCTCAGA	63891
rs200858463	snp	C/T	1.6588e-05	0.00287988	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705652	GGTCATGATGTACAA[C/T]CTCAGCGTACACCAG	63891
rs200860833	snp	C/G	0.000397797	0.0140975	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712506	GACATCTACTGGCTG[C/G]TGCGCGTCTGCCTGC	63891
rs200902567	snp	C/G	0.000399281	0.0141238	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718987	CCCAGGTAGAGATGG[C/G]TGAGCGCGCGCAGGC	63891
rs200940783	in-del	-/A	0.0236746	0.106192	intron-variant	RNF123	GRCh38.p7	3:49713270	GTGTGTGCTGAGATG[-/A]GGTTTGAGCCCAGGT	63891
rs200992117	snp	A/G	0.00105817	0.0229775	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721716	CTCCCCTTGCTGATG[A/G]GAAAACCGGGGCTCG	63891
rs201060216	snp	A/G/T	0.000283579	0.0119045	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713551	CTGGCTGCCATTCTC[A/G/T]CCAAACACTTTGCCG	63891
rs201096152	snp	C/T	0.000347613	0.013179	intron-variant	RNF123	GRCh38.p7	3:49702069	GAGGGCCATGTTCCT[C/T]ACCTGACCTCCAGTG	63891
rs201104028	snp	C/T	1.65007e-05	0.00287229	intron-variant	RNF123	GRCh38.p7	3:49700380	ACCTCAGGCCTCAGG[C/T]CTGGCTGTCAGTCTT	63891
rs201130976	snp	A/G	3.30868e-05	0.00406723	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691434	GCTCAGGCATTGTGC[A/G]GGAGAAGCTGCTGAA	63891
rs201139383	snp	A/C	0.000449914	0.0149918	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687801	TCTTCAGCATCTGCC[A/C]CATCCTCCTGCCAAG	63891
rs201142400	snp	C/G	8.32799e-05	0.00645236	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719151	GCCGCTGGCGTTGAC[C/G]AAGACGCCGCGACCC	63891
rs201152067	snp	C/G/T	0.00201833	0.0317036	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691521	GCAGGTATGGCTGGG[C/G/T]GGGTGGCCCCTCCTC	63891
rs201194748	snp	C/T	6.62636e-05	0.00575564	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700258	TGGAGGCTGTGCTCA[C/T]GAGCTTCTTGCTGGG	63891
rs201209187	snp	C/T	0.000889313	0.0210681	intron-variant	RNF123	GRCh38.p7	3:49700620	CCTGTCCACTCTGAA[C/T]GCCCCCTCTCCACAG	63891
rs201247664	snp	A/G	8.32161e-05	0.00644989	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698757	CCTCTCATGGCAGGC[A/G]TGGGCAGCGGGGGAC	63891
rs201260267	snp	C/T	0.00199806	0.0315443	synonymous-codon, intron-variant, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721887	CTCCATGCGTACCTC[C/T]AGGAGAGGATAGGCC	63891
rs201261057	in-del	-/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49689889	TGACAGGGAGTCCCC[-/G]GGGCGGGGACAAGGT	63891
rs201279099	snp	A/C	1.64803e-05	0.00287052	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712609	TCAACAGCTACAGTG[A/C]TCTCAAGAATTACTT	63891
rs201346101	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49696922	AAGTGCTGGGATTAC[A/G]GGCATGGGCCACCAC	63891
rs201357944	snp	G/T	0.000557378	0.0166847	intron-variant	RNF123	GRCh38.p7	3:49713688	TGGGCATGAAGTATG[G/T]GTCCAGGGCTCATGC	63891
rs201373126	snp	A/G	1.66743e-05	0.00288736	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719419	GGGGTGCCTAACCCA[A/G]CGCGCAGCATGCAGA	63891
rs201383686	snp	A/G	3.29549e-05	0.00405911	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720820	GATTATATCAGTGCC[A/G]ATGAGCTGGCCCAAG	63891
rs201393611	snp	C/T	1.66389e-05	0.0028843	intron-variant	RNF123	GRCh38.p7	3:49699633	TTCCACAGCCTCCTG[C/T]CCCTCACACTTCTCC	63891
rs201466020	snp	G/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700677	CATCCTGAGGCATGA[G/T]AAGTCCCGCAAGTTT	63891
rs201473991	snp	C/T	0.000148776	0.00862357	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701824	AGGGCAAAGAGAGCA[C/T]GGAGATGAAGGAGGA	63891
rs201479576	snp	C/G/T	1.70936e-05	0.00292344	intron-variant, synonymous-codon, missense	RNF123, AMIGO3	GRCh38.p7	3:49718653	GGCCGACGAGCAGTT[C/G/T]TCAAAGACGCGGCTG	63891
rs201480353	snp	A/G	1.8541e-05	0.00304469	intron-variant	RNF123	GRCh38.p7	3:49697472	GGTGAGTGAGGGTGA[A/G]GTGTGGAGACCCAGG	63891
rs201494840	snp	G/T	1.6784e-05	0.00289685	intron-variant	RNF123	GRCh38.p7	3:49705692	AAGGTCGTGCACTCT[G/T]GGACCCCGCATTGGG	63891
rs201531875	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49705349	GAGATCAATGCCGCA[G/T]AAATAGGTCCTGGCA	63891
rs201534843	snp	A/G/T	6.59454e-05	0.00574187	intron-variant	RNF123	GRCh38.p7	3:49703556	CTGTGGGCCGGGAGC[A/G/T]GTTCTGGGGCCAGGT	63891
rs201540431	snp	C/T	3.3095e-05	0.00406773	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719018	CGTGGAAGGCATGCT[C/T]GTCCAAGTGCACCAA	63891
rs201567126	snp	A/T	0.00473907	0.0484466	intron-variant	RNF123	GRCh38.p7	3:49702040	CCAAACCTGCCCCCC[A/T]TCTCCTGGAGCCTGA	63891
rs201576562	in-del	-/A	0.00835141	0.0640778	intron-variant	RNF123	GRCh38.p7	3:49700038	CGTGTGCCAAGCCTT[-/A]AGAGGAGCCGTGGGG	63891
rs201611868	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49693672	AATTTTTAGTTTTTT[C/G]AGGAACCTCCAAACT	63891
rs201620892	snp	A/G	5.07799e-05	0.00503859	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718268	GGGCGAACAGGTAGA[A/G]CAGCACGAGCACAAG	63891
rs201729350	snp	A/G	8.2558e-05	0.00642434	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698987	CTCCCCAGGAACGGT[A/G]TATCACTGGGCACTG	63891
rs201733026	snp	C/T	0.000463814	0.0152214	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712509	ATCTACTGGCTGCTG[C/T]GCGTCTGCCTGCGGA	63891
rs201762043	snp	A/C	0.000585505	0.0171	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718871	CCAGCTCAGGTACGG[A/C]GATGTGTCCCAGCCG	63891
rs201809006	snp	A/G/T			missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691187	TCCAAGGGGGCCGGC[A/G/T]TGTCTTTCTCCCGCA	63891
rs201817210	snp	C/T	8.24722e-05	0.006421	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712546	AGCACGGTGATCGCA[C/T]AGGGTCTCTCTTTGC	63891
rs201822390	snp	A/G	1.75965e-05	0.00296613	intron-variant	RNF123	GRCh38.p7	3:49712453	ACTGGTGCGCAACCC[A/G]GCAGCACCCCGTGTG	63891
rs201830526	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49712696	CAGAAGCAGAAAAGG[C/G]GTCTCTAGTGTGAGC	63891
rs201833731	snp	A/G	0.00927396	0.0674609	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687653	ACCATGGCTGCTCAC[A/G]TTGTAGTGGAAGGCC	63891
rs201865623	snp	C/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49715902	CACCTGCTTTGACCT[C/G]TCGGTCAGCCTGCTG	63891
rs201901135	snp	A/G	7.68275e-05	0.00619741	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705130	GCCTCTGAGCACCTC[A/G]GAGAAAGTGAAGGTC	63891
rs201904749	snp	C/T	0.000181256	0.00951816	intron-variant	RNF123	GRCh38.p7	3:49700460	TGGCTGCCTTGGCAT[C/T]TCTTCCCCCAGGACT	63891
rs201961378	snp	A/G	0.00180346	0.0299746	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720671	GAGTGGGCTGGTGGG[A/G]CAGGTCAGGGAAATC	63891
rs202013612	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690107	TGGTGCAGACCCACA[A/G]GGGTTTGTGGCGGGA	63891
rs202032649	snp	A/G	0.0018272	0.0301706	intron-variant	RNF123	GRCh38.p7	3:49700571	GGCCTACAGGTGGGA[A/G]CCCCTACCCCTGCCC	63891
rs202035016	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49703498	CAGCGCCTGGGGGGC[C/T]TCCTCTCGCACCTGC	63891
rs202083771	snp	A/T			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713783	CCAGCTACGTGTGCT[A/T]CCCACACTCCCTGCG	63891
rs202116551	snp	C/T	4.95479e-05	0.0049771	intron-variant	RNF123	GRCh38.p7	3:49715734	GCTGTGGTGGGGCCT[C/T]GTGGGTTAGGGTGGT	63891
rs202151835	snp	G/T	0.000111516	0.00746629	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721712	AGCACTCCCCTTGCT[G/T]ATGGGAAAACCGGGG	63891
rs202178447	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49700115	TGTTTGGTGTTGCTC[A/G]AGTGGCTCAAGGCTC	63891
rs202201340	snp	C/G	1.66277e-05	0.00288333	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719120	ACGTGTTAGATGATA[C/G]ATCGAGCAGCCTCAG	63891
rs202217238	in-del	-/G			intron-variant	RNF123	GRCh38.p7	3:49695258	CAAGCACATGCCACA[-/G]CACCCAGCTAATTTT	63891
rs267599875	snp	C/T	2.68064e-05	0.00366094	RNF123	3	allele_origin=T(somatic)/C(germline)	3:49704681	AGCCAACATTGTGAT[C/T]GACCCACTGGAGCTC	63891
rs367664871	snp	C/G	6.68963e-05	0.00578305	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718172	TGAGTACTGAGGACT[C/G]TGCGCTCAGCTCTTG	63891
rs367682711	snp	C/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49697848	GAGATGCTCTGTGTG[C/T]CTGGGAGCTAGCCCA	63891
rs367730914	snp	A/G	1.65592e-05	0.00287738	downstream-variant-500B, missense, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721060	CCATCTGCTATGCCC[A/G]CCCCATCTCTGCTGT	63891
rs367737232	snp	C/T	4.94271e-05	0.00497102	intron-variant	RNF123	GRCh38.p7	3:49700603	GAGCCCCCTGGGACT[C/T]GCCTGTCCACTCTGA	63891
rs367752442	snp	C/T	6.60426e-05	0.00574604	intron-variant	RNF123	GRCh38.p7	3:49714078	CCTGGGCACTGACCC[C/T]CACCTCCACAGGGCT	63891
rs367820087	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721571	AGTGGGGTTTGTGGG[A/G]TGTGCCCAGCAGGGA	63891
rs367826196	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49696864	GTGGCCAGGCTGGTC[C/T]CGAACTCCTGACCTC	63891
rs367832292	snp	A/C/G	3.41723e-05	0.0041334	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718757	CGGCGCTCAGGCCCC[A/C/G]CTGGTGCCAGCGCTG	63891
rs367853996	snp	A/G	1.65985e-05	0.00288079	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687661	TGCTCACGTTGTAGT[A/G]GAAGGCCCTGGAGAG	63891
rs367894114	snp	C/T	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720506	TTGCACCCTCCCCTA[C/T]CTAGGAGAGAGCAAG	63891
rs367894311	snp	A/G	1.64882e-05	0.00287121	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712566	TCTCTCTTTGCCTTC[A/G]TGCCCGAGTTCTACC	63891
rs367898854	snp	C/T	3.40153e-05	0.0041239	intron-variant	RNF123	GRCh38.p7	3:49699605	GGGGTCTGGGCCAGG[C/T]GGGGTGGGGGGCTTC	63891
rs367919605	snp	A/G	0.00108758	0.023294	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720909	GGTGAGTGGGAACAC[A/G]GTGCACAGGTCCATG	63891
rs367919738	snp	A/C	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49716052	GGACCCTGGGGATGC[A/C]CCATTGATGACGCTC	63891
rs367942261	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49696750	CACCAAGGTTCAAGC[G/T]ATTCTCCTGCCTCTG	63891
rs367979932	snp	C/T	0.000165873	0.00910544	intron-variant	RNF123	GRCh38.p7	3:49702077	TGTTCCTCACCTGAC[C/T]TCCAGTGGTGGAAGA	63891
rs368028287	snp	C/T	9.22382e-05	0.00679048	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49704705	GGAGCTCCAGTCAAC[C/T]GCCATGGATGACCTA	63891
rs368043328	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49694473	GCCCTAGTTTGGAAG[G/T]ACTTTTGCTTTTGTA	63891
rs368089659	snp	A/G	1.64795e-05	0.00287045	intron-variant	RNF123	GRCh38.p7	3:49705976	ATGTGGTCCCATGCT[A/G]TGTAGATGGTGGGTG	63891
rs368090559	snp	A/G	9.92195e-05	0.00704272	intron-variant	RNF123	GRCh38.p7	3:49714011	GGGTAAGCCTGACTC[A/G]AGGGGAAGTGGCTGA	63891
rs368148913	snp	A/T	1.6525e-05	0.00287441	intron-variant	RNF123	GRCh38.p7	3:49698530	AATTATGGCAAGGTG[A/T]GAGCCAAGCCCCTGT	63891
rs368156906	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49698306	CACCCCAGCTCAGAG[A/C]ATACCTCTTACTCTT	63891
rs368207738	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49710441	TACGCCACCACGCCC[A/G]GCTAATTTTTGTATT	63891
rs368214804	snp	A/C	0.000153988	0.00877328	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718736	ACTCGCGCGCAAAGT[A/C]GCGCACGGCGCTCAG	63891
rs368223002	snp	A/G	8.59457e-05	0.00655481	intron-variant	RNF123	GRCh38.p7	3:49703550	ACAGGCCTGTGGGCC[A/G]GGAGCAGTTCTGGGG	63891
rs368287147	snp	C/T			intron-variant, utr-variant-5-prime	RNF123, AMIGO3	GRCh38.p7	3:49719609	TGCCAGCCGACGGCC[C/T]CTACTCTCCGGTTCC	63891
rs368324283	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49696617	GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT	63891
rs368358056	snp	C/G/T	0.000115495	0.00759846	intron-variant	RNF123	GRCh38.p7	3:49702445	CTGTGGATCCCCGGC[C/G/T]GCACTACACATGCCA	63891
rs368485481	snp	C/G/T	0.000121486	0.00779302	intron-variant	RNF123	GRCh38.p7	3:49705220	CAGGTCCCCGAAGGA[C/G/T]CCTTCCACAGTGTAC	63891
rs368572178	snp	A/C	3.36825e-05	0.00410367	intron-variant	RNF123	GRCh38.p7	3:49705697	CGTGCACTCTTGGAC[A/C]CCGCATTGGGTGGCG	63891
rs368579233	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49715503	AAAGCCTCAATGGGC[A/G]AGGACAGAGGCAAAC	63891
rs368682889	snp	C/T	1.66026e-05	0.00288115	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687703	GGGTAACGCCACAGC[C/T]CAGGCTTCCCTGCCC	63891
rs368696011	snp	C/T	0.00318978	0.0398085	intron-variant	RNF123	GRCh38.p7	3:49711540	TAGCAGCAGGATCAT[C/T]GCTGCCTAGGTTTGC	63891
rs368723431	snp	A/G	0.000132639	0.0081426	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713917	CCTCACAGGCGTATC[A/G]CCATGGTGAGGAACC	63891
rs368732012	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49715136	CCAAGGCCAGGCCAA[A/G]GGCAGCAGAGGACAG	63891
rs368742946	snp	C/T	0.000216603	0.0104046	intron-variant	RNF123	GRCh38.p7	3:49716063	ATGCCCCATTGATGA[C/T]GCTCCCCATCCACCA	63891
rs368745565	snp	G/T	1.66557e-05	0.00288575	intron-variant	RNF123	GRCh38.p7	3:49698404	GCCCAGACCCTGCCT[G/T]CCTCACCAGGGACCT	63891
rs368752247	snp	C/T	1.65965e-05	0.00288062	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687745	TAGGCCCAGTGGCCA[C/T]TCACCGGCAGTCCAT	63891
rs368796906	snp	C/T	3.30912e-05	0.00406749	intron-variant	RNF123	GRCh38.p7	3:49698975	AGACCCACCCTTCTC[C/T]CCAGGAACGGTGTAT	63891
rs368808320	snp	A/G	1.68778e-05	0.00290493	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718471	AAGCTGCCGTCGGCC[A/G]GCACCGCGATGCTGC	63891
rs368813031	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49706062	CCGCCGGTGCCCCAA[A/G]AGGGTAAGGCCCACA	63891
rs368827884	snp	A/G	0.000203163	0.0100767	intron-variant	RNF123	GRCh38.p7	3:49698710	GTTCAGAGTCAGCAG[A/G]CTGCTGGGCTTCTGT	63891
rs369008658	snp	A/G	4.97525e-05	0.00498736	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687421	AGGCCACCCACGGTC[A/G]TGGCCATGGTGCCCC	63891
rs369134155	snp	A/C/G	0.00278602	0.0372198	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687683	CCTGGAGAGAAGAAG[A/C/G]CACAGGGTAACGCCA	63891
rs369164501	snp	A/G	1.66479e-05	0.00288508	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701495	ACACCCGCCAGCTTC[A/G]ACGTGCTCCGCTCCG	63891
rs369165447	snp	C/G	4.94539e-05	0.00497238	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720903	CTCCCTGGTGAGTGG[C/G]AACACGGTGCACAGG	63891
rs369182780	snp	C/T	1.71425e-05	0.00292762	intron-variant	RNF123	GRCh38.p7	3:49700203	GGAAGGCCACCACCT[C/T]ACCAGTGCCTGGCCT	63891
rs369187602	snp	C/G	6.58892e-05	0.00573936	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702653	GCCCATGCTCTGCCC[C/G]CCTGAGTACATGGTC	63891
rs369192919	snp	C/T	0.00199481	0.0315187	intron-variant	RNF123	GRCh38.p7	3:49712087	AAAATTAGCCGAGCG[C/T]GGTATCACATACCTG	63891
rs369228844	snp	C/G	0.000153988	0.00877328	synonymous-codon, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721845	CTCATCATTAACTAT[C/G]ACGTCCTCACCCAGC	63891
rs369353080	snp	C/G	5.0048e-05	0.00500215	intron-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691266	AGAGCTGGCAGGGAA[C/G]GAAGGAGGCTCCTCT	63891
rs369359759	snp	C/T	5.06598e-05	0.00503263	intron-variant	RNF123	GRCh38.p7	3:49714219	CAAGGCAGGCGGGGG[C/T]GCTTACCTCCTACCC	63891
rs369371695	snp	C/T	3.29506e-05	0.00405884	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700648	CAGATCCATTACCTG[C/T]GGCTCACTATCGCCA	63891
rs369412191	snp	C/T	1.68926e-05	0.0029062	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49716168	CGTGTGGTCACCCTA[C/T]GGCTGCCTGGTGAGG	63891
rs369499883	snp	C/T	3.60023e-05	0.00424262	intron-variant	RNF123	GRCh38.p7	3:49712445	AAGACCCCACTGGTG[C/T]GCAACCCAGCAGCAC	63891
rs369530050	snp	C/G	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49698289	TCCCACCCAATCCCA[C/G]GCACCCCAGCTCAGA	63891
rs369539041	snp	C/T	0.000131835	0.00811788	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49712607	CATCAACAGCTACAG[C/T]GCTCTCAAGAATTAC	63891
rs369613782	snp	C/T	0.000899116	0.0211837	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687303	GAGGGCCCAGAGCAT[C/T]ACTATAGTGTGTGCT	63891
rs369643825	snp	C/T	2.28548e-05	0.00338037	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705061	TTCTCCAACTTTGGG[C/T]CGAGCCAACCGCTTC	63891
rs369735582	snp	A/G	0.000798403	0.0199641	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716782	GTGCCGTCCTGTGGT[A/G]GACAGGGCCAGGCCG	63891
rs369742686	snp	C/G/T	3.29507e-05	0.00405887	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700639	CCCTCTCCACAGATC[C/G/T]ATTACCTGCGGCTCA	63891
rs369743745	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49693953	TTTGATGGAATTATT[A/C]GTTTTTTTCCTATAG	63891
rs369784049	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49706657	TCAGTGGCAGAAGAA[C/G]GTTTTGAAAAATGGA	63891
rs369945756	snp	A/T	0.00636936	0.0560724	intron-variant	RNF123	GRCh38.p7	3:49711011	GCTGAAGCGGGAGGA[A/T]CACTTGAAGCCAAGA	63891
rs369974257	snp	A/C/G	0.000517516	0.016078	intron-variant	RNF123	GRCh38.p7	3:49699657	CTTCTCCCTCCTCCC[A/C/G]CTCCACACAGGAGGG	63891
rs370014658	snp	C/G	1.67385e-05	0.00289292	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718328	AGCCTGTGTTGAAAG[C/G]CTCGGGCTCTGGGCG	63891
rs370027636	snp	C/G	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49698014	GAGGCAAGAGGCAGT[C/G]TTTGTCCACCTCGTG	63891
rs370032522	snp	C/G	1.77316e-05	0.0029775	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720532	GCAAGCCACATCAGT[C/G]CTCCTGGCAGATCCC	63891
rs370078820	snp	C/T	3.29826e-05	0.00406082	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720921	CACGGTGCACAGGTC[C/T]ATGCCACTTGAATAT	63891
rs370096301	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702695	CCGGCTGATCTCTGC[C/T]CTGCGCTACTATTGG	63891
rs370100467	snp	G/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49697247	CACCTCTGGAGTGGG[G/T]TTGGGAGGTGCAGAG	63891
rs370111411	snp	G/T	6.0033e-05	0.0054784	intron-variant	RNF123	GRCh38.p7	3:49704767	CCCAGGTGCCGCAGT[G/T]GGGGCAGGCGGTGGG	63891
rs370209625	snp	A/G	0.000233372	0.0107996	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712483	GCCTCCTGCAGGAGA[A/G]GATGCTGGACATCTA	63891
rs370220989	snp	A/G	1.6604e-05	0.00288127	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698773	TGGGCAGCGGGGGAC[A/G]TCGTGAGCTGCCTGA	63891
rs370250116	snp	C/T	9.98502e-05	0.00706506	intron-variant	RNF123	GRCh38.p7	3:49716056	CCTGGGGATGCCCCA[C/T]TGATGACGCTCCCCA	63891
rs370283169	snp	C/G/T	5.26989e-05	0.00513295	missense, synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699571	GTGCTGAGTGTGGAG[C/G/T]TGGACCCTGTGGTGA	63891
rs370292979	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688693	CACCACAGCCCCATC[C/G]GGGAAGTTGTGAAAC	63891
rs370368339	snp	C/T	4.98517e-05	0.00499233	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705116	ATGACCCCACGGCGG[C/T]CTCTGAGCACCTCGG	63891
rs370438853	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720317	GAGACTCGTCTCAAG[-/AA]AAAAAAAAAAAAAAA	63891
rs370460760	snp	C/G	4.97624e-05	0.00498786	intron-variant	RNF123	GRCh38.p7	3:49702080	TCCTCACCTGACCTC[C/G]AGTGGTGGAAGAACT	63891
rs370494504	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49713122	CCAGGCTGGGCGTGG[C/T]AGTGTATGTCTGGAT	63891
rs370533536	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49692644	TACCCTTCCAAGCCT[C/G]TGGTAACCATCCAGT	63891
rs370548567	snp	G/T	1.65064e-05	0.00287279	intron-variant	RNF123	GRCh38.p7	3:49702457	GGCTGCACTACACAT[G/T]CCATGCCCTCAGCAC	63891
rs370553769	snp	C/T	6.23539e-05	0.00558328	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699523	AGTGCTGACCTGGTG[C/T]GGGCACAGAGGTTGC	63891
rs370680718	snp	A/G	5.67746e-05	0.00532767	intron-variant	RNF123	GRCh38.p7	3:49697478	TGAGGGTGAGGTGTG[A/G]AGACCCAGGTCCAGC	63891
rs370723406	snp	C/T	1.85527e-05	0.00304565	intron-variant	RNF123	GRCh38.p7	3:49691531	CTGGGTGGGTGGCCC[C/T]TCCTCACTCTGCTGG	63891
rs370738203	snp	C/G/T	0.000371105	0.0136171	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721723	TGCTGATGGGAAAAC[C/G/T]GGGGCTCGGCCAGCC	63891
rs370796813	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49695184	CATAGCTCACTGCAA[C/T]CTCAAAGTCCCAGGC	63891
rs370840348	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49706081	GTAAGGCCCACATAG[C/T]CTTGGTGAGGGGCAG	63891
rs370851925	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49715868	ACTTTGTGGACAGCC[A/G]GCAGCTCAAGGTATG	63891
rs370891487	snp	A/G/T	3.31078e-05	0.00406854	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687600	GAACGCCGCAGCCTC[A/G/T]TGTGGGGCGAGTGTT	63891
rs370922623	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49709102	TGGGACTACAGGTGC[G/T]CACCACCATGCTCGG	63891
rs371007145	snp	C/T	4.96537e-05	0.00498241	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719005	AGCGCGCGCAGGCCG[C/T]GGAAGGCATGCTCGT	63891
rs371025305	snp	C/T	3.30775e-05	0.00406665	intron-variant	RNF123	GRCh38.p7	3:49714010	AGGGTAAGCCTGACT[C/T]GAGGGGAAGTGGCTG	63891
rs371028552	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49714949	TCCTGCGTCCAGGGC[A/G]GAACTGAGCTGCAAG	63891
rs371035008	snp	A/G	3.29592e-05	0.00405938	intron-variant	RNF123	GRCh38.p7	3:49700456	GTCATGGCTGCCTTG[A/G]CATCTCTTCCCCCAG	63891
rs371085589	snp	C/G	1.82947e-05	0.00302441	intron-variant	RNF123	GRCh38.p7	3:49705490	GCAGGCTCAGGAGAG[C/G]CGGGATGGCCCTACC	63891
rs371105583	snp	G/T	3.67141e-05	0.00428435	intron-variant	RNF123	GRCh38.p7	3:49697468	TGGGGGTGAGTGAGG[G/T]TGAGGTGTGGAGACC	63891
rs371188899	snp	A/G	6.63658e-05	0.00576008	missense, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721985	GACCCACGCGGCAGC[A/G]CCAGCCCACAATGCA	63891
rs371213756	snp	C/T	0.000182735	0.00955688	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687530	GTCCCCTGTCTCCCA[C/T]CCTGCCCCTCTCCAC	63891
rs371254158	snp	A/T	1.65378e-05	0.00287552	downstream-variant-500B, missense, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721096	AGCCCTGTGGCCACA[A/T]GTCCTGCAAGTAAGT	63891
rs371278564	snp	A/G	1.79226e-05	0.00299349	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705539	AACTCCCCAGTTGAA[A/G]GCAGCCACTGGAATG	63891
rs371280884	snp	A/G	1.73727e-05	0.00294721	intron-variant	RNF123	GRCh38.p7	3:49705723	TGGCGGGTGTTGTGC[A/G]TGTTTGGTTGTGTGT	63891
rs371347770	snp	A/G	0.000155988	0.00883005	intron-variant	RNF123	GRCh38.p7	3:49701761	GAGTGAAGGAGGCCT[A/G]GCTAGGTCCCAGGTG	63891
rs371379790	snp	A/G/T	6.79827e-05	0.00582989	intron-variant, stop-gained, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718599	CCGACCCACCAGCGC[A/G/T]TACAGGTGCTCTTCC	63891
rs371440681	snp	C/T	9.91522e-05	0.00704033	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49698983	CCTTCTCCCCAGGAA[C/T]GGTGTATCACTGGGC	63891
rs371463148	snp	A/G			intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717059	GAGGCTCCTGCTCTC[A/G]AGGGACGTGGAGTTC	63891
rs371464906	snp	G/T	1.66062e-05	0.00288146	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687690	AGAAGAAGGCACAGG[G/T]TAACGCCACAGCCCA	63891
rs371501091	snp	C/G	0.00517822	0.0506191	intron-variant	RNF123	GRCh38.p7	3:49691595	GAAAGGGAGCCTGGG[C/G]TCTGGACAGATAGGC	63891
rs371586883	snp	C/G	0.000399281	0.0141238	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716594	GGACCTCAGCATCAG[C/G]TTTTGAGGCAGAGGG	63891
rs371594000	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690021	AACTACTCTGGTAGT[A/G]AAGGGGCACCGATCA	63891
rs371617721	snp	C/T	7.47021e-05	0.0061111	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713817	TGTGGAGCGAATCCC[C/T]GAGGAGCAGTGAGTG	63891
rs371632157	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49701078	TTGGGAACTGCATGA[C/G]TGAGTGAGAGCATAG	63891
rs371656831	snp	A/G			missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687613	TCGTGTGGGGCGAGT[A/G]TTGAGTCCATGGCAG	63891
rs371662347	snp	C/T	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49709551	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	63891
rs371665827	snp	A/C/T	0.000115521	0.00759931	synonymous-codon, missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49714117	GGGTACCGCTATACA[A/C/T]GGCTGCCACATCTGC	63891
rs371690410	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49703864	CAGCGAGAGCAAGGC[A/C]CTGAGCCGGGCACAA	63891
rs371778146	snp	C/T	1.83246e-05	0.00302687	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720508	GCACCCTCCCCTACC[C/T]AGGAGAGAGCAAGCC	63891
rs371862537	snp	C/T	1.78449e-05	0.00298699	intron-variant, utr-variant-5-prime	RNF123, AMIGO3	GRCh38.p7	3:49719497	GACAGTACAGAGCAG[C/T]TCTGTGCAGGTTGCA	63891
rs371924160	snp	C/G/T	6.6127e-05	0.00574976	missense, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716461	GTGCAGCTCCTGGTG[C/G/T]GTGGCCCAGCCTCAG	63891
rs371925287	snp	C/T	0.000153988	0.00877327	intron-variant	RNF123	GRCh38.p7	3:49704761	CTATGGCCCAGGTGC[C/T]GCAGTGGGGGCAGGC	63891
rs371933757	snp	A/T	0.00147974	0.0271603	intron-variant	RNF123	GRCh38.p7	3:49701946	GGGTAGGGTGGGAGG[A/T]GTGTGTGTGCACATG	63891
rs372013548	snp	A/G	0.000153988	0.00877328	downstream-variant-500B, missense, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721271	AGGACTGGGAGAAGG[A/G]AGCCAATACGAGTAC	63891
rs372022358	snp	A/G	0.0252325	0.109451	intron-variant	RNF123	GRCh38.p7	3:49708707	CCTCAAGGTTCATTC[A/G]TGTTATAGCATGTGT	63891
rs372026114	snp	A/G	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49714177	CCCAGCCTCCAGAGT[A/G]AGTATCTGGGTTGGG	63891
rs372030150	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49700645	CCACAGATCCATTAC[C/T]TGCGGCTCACTATCG	63891
rs372037773	snp	C/T	1.66305e-05	0.00288357	downstream-variant-500B, intron-variant, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49720999	CCAACTCCAGCCCAC[C/T]CTTCACTCTCCTCCC	63891
rs372040126	snp	C/T	8.23716e-05	0.00641709	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49706017	TGTCAATGAATACGC[C/T]ATGGCTCTGAGGGAC	63891
rs372044265	snp	C/T	0.000149423	0.0086423	intron-variant	RNF123	GRCh38.p7	3:49698554	CCCCTGTGGGTCATC[C/T]GCCCCATGACTGTTA	63891
rs372046511	snp	A/G	1.65302e-05	0.00287486	intron-variant	RNF123	GRCh38.p7	3:49714050	GGAGGGAGAGGGTGC[A/G]CTGTCCCATTGACCT	63891
rs372047131	snp	C/T	1.65803e-05	0.00287922	intron-variant	RNF123	GRCh38.p7	3:49698426	CAGGGACCTCATAGG[C/T]ATTTCCTCCCTAGGA	63891
rs372222420	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702370	TTCCTGACCAAGTTT[C/T]GCAAGTTTCTGCAGG	63891
rs372252354	snp	A/G	1.88642e-05	0.00307111	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699540	GGCACAGAGGTTGCT[A/G]GGCTGCTTCCGGGCA	63891
rs372289594	snp	A/C/G	7.08466e-05	0.00595133	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687888	AAGTCATTCAATGGC[A/C/G]AGCGCTGCCCTGCAG	63891
rs372306225	snp	C/T	0.000153988	0.00877328	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718754	GCACGGCGCTCAGGC[C/T]CCGCTGGTGCCAGCG	63891
rs372308351	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690200	GCAGTGCTGCAGAGC[A/G]AAACTCTAGACCTGC	63891
rs372312226	snp	A/G	0.000284306	0.0119194	intron-variant	RNF123	GRCh38.p7	3:49703562	GCCGGGAGCAGTTCT[A/G]GGGCCAGGTGGGGGA	63891
rs372368983	snp	C/T			intron-variant, utr-variant-5-prime	RNF123, AMIGO3	GRCh38.p7	3:49719617	GACGGCCCCTACTCT[C/T]CGGTTCCCAGGTTGT	63891
rs372415898	snp	A/G/T	0.000445081	0.0149116	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705030	CACTGCCCCTGCCCC[A/G/T]GCCCGGCTGGCTCAG	63891
rs372491482	snp	C/T	8.43519e-05	0.00649375	intron-variant	RNF123	GRCh38.p7	3:49705699	TGCACTCTTGGACCC[C/T]GCATTGGGTGGCGGG	63891
rs372512288	snp	C/T	1.65225e-05	0.00287419	missense, splice-acceptor-variant, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721885	TTCTCCATGCGTACC[C/T]CCAGGAGAGGATAGG	63891
rs372521579	snp	C/T	6.65657e-05	0.00576875	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701497	ACCCGCCAGCTTCGA[C/T]GTGCTCCGCTCCGTC	63891
rs372521905	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49695955	TTGGCTCGGGTAGGT[A/G]GGTCATGTGCTCCGC	63891
rs372575178	snp	C/T	8.71878e-05	0.00660199	intron-variant	RNF123	GRCh38.p7	3:49701918	CATCGAAGGTCAGCC[C/T]GCCTTGGGCACGGGG	63891
rs372588038	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49706515	CAGCTGGGGGAGCAG[C/T]GGTTCTGGCATCAGG	63891
rs372615638	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49715142	CCAGGCCAAGGGCAG[C/G]AGAGGACAGTAGAGG	63891
rs372660006	snp	A/G	3.68806e-05	0.00429406	utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721731	GGAAAACCGGGGCTC[A/G]GCCAGCCCCACTGCA	63891
rs372671110	snp	C/T	0.000214318	0.0103495	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720908	TGGTGAGTGGGAACA[C/T]GGTGCACAGGTCCAT	63891
rs372680929	snp	C/T	3.42296e-05	0.00413686	intron-variant	RNF123	GRCh38.p7	3:49700205	AAGGCCACCACCTCA[C/T]CAGTGCCTGGCCTTG	63891
rs372736168	snp	A/G	1.65233e-05	0.00287426	missense, intron-variant, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49721894	CGTACCTCCAGGAGA[A/G]GATAGGCCTTGTCAG	63891
rs372750601	snp	A/C/T	0.000272781	0.0116757	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720560	CCCTGCTTCCAGCTA[A/C/T]GCTCAATATGCTATC	63891
rs372770015	snp	C/T	0.0002324	0.0107771	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699674	TCCACACAGGAGGGG[C/T]GGCTGTTGGACAAGG	63891
rs372801805	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49702253	CCATGGCAGGGGCTG[A/G]GGGAAGGTGCAGCAC	63891
rs372834895	snp	C/G	5.06941e-05	0.00503433	intron-variant	RNF123	GRCh38.p7	3:49714221	AGGCAGGCGGGGGCG[C/G]TTACCTCCTACCCAT	63891
rs372846960	snp	C/T	0.000283416	0.0119007	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687341	GGCCCCAGGCCGGGA[C/T]GGAGGGAAGGTGTTT	63891
rs372914999	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49705476	TCTCCTGCTGTGAGG[C/T]AGGCTCAGGAGAGCC	63891
rs372952735	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49703023	CCGTCCTTGCCCCCC[-/C]ATTTCTCTGTGCGTC	63891
rs372982898	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49715591	GCCCTGCCCTTCCAC[C/T]CTGCTGCAGCAGCAC	63891
rs372986737	snp	C/T			intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717807	CAGTGAGCGAGAAGG[C/T]CCATTGTGTTTCGAG	63891
rs373043136	snp	C/G	0.000164766	0.00907502	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720835	GATGAGCTGGCCCAA[C/G]TGGAACAGATGCTGG	63891
rs373044849	snp	G/T	1.64803e-05	0.00287052	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49712608	ATCAACAGCTACAGT[G/T]CTCTCAAGAATTACT	63891
rs373099985	snp	A/G/T	0.000335565	0.012949	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705147	AGAAAGTGAAGGTCC[A/G/T]CACGCTGAGCGTGGA	63891
rs373109530	snp	A/G	0.000338543	0.013006	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705072	TGGGCCGAGCCAACC[A/G]CTTCCTCAGCACAGC	63891
rs373111160	snp	C/G/T	1.65949e-05	0.00288048	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718931	GGGTGGCGCTCAGAC[C/G/T]GTGCAGGTGGTCGAA	63891
rs373111527	snp	G/T	0.000153988	0.00877328	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687461	CCCCATTGTTCATGA[G/T]GCAGGTCCGTACGTA	63891
rs373111628	snp	A/C/G	3.33997e-05	0.00408643	intron-variant	RNF123	GRCh38.p7	3:49706937	CTTCCCGACCTCACT[A/C/G]TCTGGCCACGGGTCT	63891
rs373111955	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692626	TCCCCACAAGCCCTA[C/T]ACTACCCTTCCAAGC	63891
rs373123968	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49692862	TACCATGTTTTCTTT[A/C]TTTATTCATCTGTTG	63891
rs373126138	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49707172	CCCCTGCTCCCACCC[C/G]CTCCCAGTTTCTTGG	63891
rs373134885	snp	A/G	0.000437904	0.0147905	intron-variant	RNF123	GRCh38.p7	3:49702200	AGGGATGCTGCACTG[A/G]GCCTTAAGACCCAGA	63891
rs373220334	snp	C/G	1.65921e-05	0.00288024	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719081	CCCCCAGCCCGTCGA[C/G]GTCGTGGCGGCCAAG	63891
rs373223445	snp	A/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714249	CATGGGTTCTTTCAG[A/T]CTCTCCACTTCTTCC	63891
rs373323429	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700664	GGCTCACTATCGCCA[C/T]CCTGAGGCATGAGAA	63891
rs373340611	snp	A/G	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49714216	GGGCAAGGCAGGCGG[A/G]GGCGCTTACCTCCTA	63891
rs373347737	snp	C/T	0.000153988	0.00877327	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688665	CCTTCTGGCTGGAGG[C/T]TGCACTGTGACCCAC	63891
rs373359682	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49699630	GGCTTCCACAGCCTC[C/T]TGCCCCTCACACTTC	63891
rs373369688	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49710250	CCTTTACAAGCACTT[A/G]TTGGCCATTTGCATA	63891
rs373397647	snp	G/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49697094	ATTTAGTGTCATCTG[G/T]CTGATTTCAAGGACT	63891
rs373600066	snp	C/T	3.68861e-05	0.00429438	intron-variant	RNF123	GRCh38.p7	3:49713735	CACGGTGTGTCCCCG[C/T]AGACATCCGAGACTC	63891
rs373615078	snp	A/G			intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717366	GTGTTGGTGGATGGA[A/G]GGAGTCCCATTTCAC	63891
rs373626144	snp	A/T	1.6596e-05	0.00288058	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687739	CTTATCTAGGCCCAG[A/T]GGCCACTCACCGGCA	63891
rs373632493	snp	C/T	6.62252e-05	0.00575397	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49712511	CTACTGGCTGCTGCG[C/T]GTCTGCCTGCGGACC	63891
rs373687118	snp	A/G	3.30126e-05	0.00406266	intron-variant	RNF123	GRCh38.p7	3:49702158	GGGTGAGTGACTCCC[A/G]GGAGCCCTGGGTGGG	63891
rs373689365	snp	C/T			intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718598	ACCGACCCACCAGCG[C/T]GTACAGGTGCTCTTC	63891
rs373712162	snp	C/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49706946	CTCACTGTCTGGCCA[C/T]GGGTCTAGCAAGATT	63891
rs373786285	snp	A/G	0.000100078	0.00707313	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49701604	CCCACTGCTCCAGTA[A/G]GGAGGTGAGTGCACC	63891
rs373821315	snp	A/G	0.000233871	0.0108111	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718153	GCGTCTGGCGGTGTG[A/G]TGCTGAGTACTGAGG	63891
rs373872356	snp	G/T	0.00011733	0.0076584	intron-variant	RNF123	GRCh38.p7	3:49697487	GGTGTGGAGACCCAG[G/T]TCCAGCCCCTTCTGA	63891
rs373890576	snp	C/T	0.000182768	0.00955776	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687774	ATTAAGGGCCCACAG[C/T]GACCAGCACACTCTT	63891
rs373975236	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49701401	GGAGAGCTGTGGTAG[A/G]CACATCCAGGGATGG	63891
rs374069012	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49711308	ATGTGCCCAAAAGTT[A/G]TGCTCTCTCCTTCTT	63891
rs374092474	snp	C/T	4.92684e-05	0.00496304	intron-variant	RNF123	GRCh38.p7	3:49713625	ACAGGGGGAGGGGGA[C/T]GGGATGGCACCTCTG	63891
rs374107951	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688532	ACTTTTTTCTCATCC[C/T]AGAATAGGAGAATGG	63891
rs374143555	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689456	GGAAGCCATGGAGGG[A/G]GTCCCCTAGCGGAGG	63891
rs374181497	snp	G/T			intron-variant	RNF123	GRCh38.p7	3:49710818	GTTCTTGGTCTGAGG[G/T]AGGGAGGGATTATAG	63891
rs374268705	snp	G/T	3.32806e-05	0.00407912	intron-variant	RNF123	GRCh38.p7	3:49716057	CTGGGGATGCCCCAT[G/T]GATGACGCTCCCCAT	63891
rs374270205	snp	G/T	3.3145e-05	0.0040708	synonymous-codon, downstream-variant-500B	GMPPB, RNF123	GRCh38.p7	3:49722025	CCAGGAATGGGAACG[G/T]ATCCGGGCATCCCGC	63891
rs374283247	snp	G/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49715723	CCAAGAGGTGGGCTG[G/T]GGTGGGGCCTCGTGG	63891
rs374314448	snp	C/T	0.0134861	0.0810011	intron-variant	RNF123	GRCh38.p7	3:49691838	TGGCCCCAGCCTGGC[C/T]CCTTGTAGCTTCTGA	63891
rs374427687	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49694454	TGCTGTGGCCCATAC[A/C]AGTGCCCTAGTTTGG	63891
rs374505290	snp	A/G			synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49715672	CAGCGTCCTCAATCA[A/G]CTCAACTGGGCCTTC	63891
rs374538101	snp	A/G	0.000153988	0.00877328	intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718332	TGTGTTGAAAGCCTC[A/G]GGCTCTGGGCGCGGA	63891
rs374539027	snp	C/T	1.67497e-05	0.00289389	intron-variant	RNF123	GRCh38.p7	3:49705688	GGGCAAGGTCGTGCA[C/T]TCTTGGACCCCGCAT	63891
rs374545967	snp	C/T	0.000153988	0.00877328	intron-variant	RNF123	GRCh38.p7	3:49698163	GGGAGGGGACCCCTC[C/T]CTGGGCCCAGGGAGA	63891
rs374552015	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49714649	CAGATTGGAGGTTGG[C/T]CAGGTCCCCAGAGGG	63891
rs374618394	snp	C/T	0.000535968	0.0163614	intron-variant	RNF123	GRCh38.p7	3:49713869	TGGCCACAAGCACCA[C/T]GCCCAGCCTCACCCC	63891
rs374618991	snp	C/T	0.0356815	0.128715	intron-variant	RNF123	GRCh38.p7	3:49696610	CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC	63891
rs374640844	snp	C/T	6.65624e-05	0.0057686	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719144	GCCTCAGGCCGCTGG[C/T]GTTGACGAAGACGCC	63891
rs374656764	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49696713	ACAATGACACGATCT[C/T]GGCTTACTACAACCT	63891
rs374677545	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49707834	TCTGCCCTGAGATTT[C/T]CTGCCTGCCCACCTC	63891
rs374766777	snp	A/G/T	0.000788859	0.019846	intron-variant	RNF123	GRCh38.p7	3:49704762	TATGGCCCAGGTGCC[A/G/T]CAGTGGGGGCAGGCG	63891
rs374805608	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49696860	CCATGTGGCCAGGCT[C/G]GTCTCGAACTCCTGA	63891
rs374830783	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49711651	AAGCCCAGGTGCTGT[A/G]ACCGCACTCCAAGAC	63891
rs374989197	snp	A/G	3.3134e-05	0.00407012	downstream-variant-500B, missense, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721056	TGCCCCATCTGCTAT[A/G]CCCACCCCATCTCTG	63891
rs375006319	snp	C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49703928	CTGCCGCAGTGTATA[C/T]GCCGGAGTGCAGGGG	63891
rs375013985	snp	C/T	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49715127	GGCCATATGCCAAGG[C/T]CAGGCCAAGGGCAGC	63891
rs375015946	snp	A/G	1.67393e-05	0.00289299	intron-variant	RNF123	GRCh38.p7	3:49698149	GGAGGTACACGTTGG[A/G]GAGGGGACCCCTCCC	63891
rs375018446	snp	C/G	1.71935e-05	0.00293197	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720661	GCAGAGCTGTGAGTG[C/G]GCTGGTGGGGCAGGT	63891
rs375121480	snp	A/G	1.6764e-05	0.00289512	intron-variant	RNF123	GRCh38.p7	3:49714214	CTGGGCAAGGCAGGC[A/G]GGGGCGCTTACCTCC	63891
rs375127888	snp	C/T	8.26754e-05	0.00642891	downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721354	CTTTGAACCCAGAGC[C/T]AGGCTGGGCCCTATT	63891
rs375128236	snp	C/T	3.34057e-05	0.00408678	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687217	GTGTAGCACCAAGGA[C/T]CTCCGGGGTCGCCAT	63891
rs375162605	snp	C/G	8.23676e-05	0.00641693	downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721308	CTCAGCTGCCTAGCC[C/G]TCACAGCCTGTGCCA	63891
rs375193155	snp	C/G	0.000140023	0.00836613	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713538	GACCCTGACCCGCCT[C/G]GCTGCCATTCTCGCC	63891
rs375193532	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49708795	ATATATCCAGTCCTT[C/T]GCTGATGGACACTCG	63891
rs375249179	snp	C/T	1.6717e-05	0.00289106	intron-variant	RNF123	GRCh38.p7	3:49716092	CAATGGACTCCTGCT[C/T]CCCTCACAGCTGCTA	63891
rs375257714	snp	C/T	8.24097e-05	0.00641857	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49702390	GTTTCTGCAGGAGAA[C/T]GCCAGTGGCCGGGGG	63891
rs375280606	snp	C/T	3.54899e-05	0.00421233	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49699564	CCGGGCAGTGCTGAG[C/T]GTGGAGCTGGACCCT	63891
rs375330458	snp	C/G	0.00107307	0.0231384	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688581	GGCAGATGGGGATCA[C/G]GGTTGGGGGCACTTA	63891
rs375331414	snp	A/G	3.67769e-05	0.00428802	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720505	CTTGCACCCTCCCCT[A/G]CCTAGGAGAGAGCAA	63891
rs375394376	snp	A/G			upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690377	AATTTAAGTAACCTC[A/G]TGTGGATGACGGCTG	63891
rs375430415	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49707122	GTTCGCCTCATAGAC[C/G]TGTCCTTCGAGGAAC	63891
rs375433707	snp	G/T	4.94833e-05	0.00497385	intron-variant	RNF123	GRCh38.p7	3:49702435	GGCCAGCCCACTGTG[G/T]ATCCCCGGCTGCACT	63891
rs375544549	snp	C/T	0.000307953	0.0124049	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720973	CAACGGACATCCACA[C/T]AGCCAGGCATCCAAC	63891
rs375549143	snp	A/G	3.30071e-05	0.00406232	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49700321	AGTCCGTGGTGCACC[A/G]GGTCCTGGACCTCTT	63891
rs375706823	snp	A/G	1.70968e-05	0.00292371	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718676	CGCGGCTGTGCTGGA[A/G]GAAGCGCACGCGGGA	63891
rs375713809	snp	A/C/T	0.000424131	0.0145565	intron-variant	RNF123	GRCh38.p7	3:49703540	AAAGGTGTGTACAGG[A/C/T]CTGTGGGCCGGGAGC	63891
rs375733364	snp	C/T	1.73951e-05	0.00294911	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688551	ATAGGAGAATGGGGC[C/T]AACCCCCTCCTGAAG	63891
rs375743436	snp	A/G	8.29607e-05	0.00643999	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699711	CCAAGTGGCGGTTGC[A/G]GGGCCAGCCCACCGT	63891
rs375767853	snp	G/T	3.32242e-05	0.00407566	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687533	CCCTGTCTCCCACCC[G/T]GCCCCTCTCCACCCC	63891
rs375829243	snp	A/G	0.00018811	0.00969636	intron-variant	RNF123	GRCh38.p7	3:49712464	ACCCAGCAGCACCCC[A/G]TGTGCCTCCTGCAGG	63891
rs375884848	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49706224	CAGCAAGGCCTGGCA[C/T]CCATCACCAGTGTGG	63891
rs375914612	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49692457	AATGGGGTATCCATC[C/T]CCTCAAGCATTTATC	63891
rs375973851	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49698850	TCTCTATGCACAGGC[C/G]TGGCCCCTGGGGCCT	63891
rs375982983	snp	A/G	1.66877e-05	0.00288852	intron-variant	RNF123	GRCh38.p7	3:49699775	TGCACCGCTTCTGGT[A/G]AGCGGCATTGGGAGG	63891
rs376007228	snp	A/C	0.00018125	0.009518	missense, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720855	ACAGATGCTGGCGCA[A/C]CTGACCTCTGCATCT	63891
rs376012553	snp	C/T	0.000103536	0.00719424	intron-variant	RNF123	GRCh38.p7	3:49700195	ACCAGAGTGGAAGGC[C/T]ACCACCTCACCAGTG	63891
rs376062454	snp	C/T	0.000153988	0.00877327	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49705152	GTGAAGGTCCGCACG[C/T]TGAGCGTGGAGCAGA	63891
rs376153434	snp	C/G	2.18252e-05	0.00330335	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713582	ACGCACGCATTGTGG[C/G]CACTGGTGAGGGGCC	63891
rs376158230	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49713117	TGATTCCAGGCTGGG[A/C]GTGGCAGTGTATGTC	63891
rs376175713	snp	A/G			intron-variant, synonymous-codon	RNF123, AMIGO3	GRCh38.p7	3:49718281	GAGCAGCACGAGCAC[A/G]AGGCCCACGGCACAG	63891
rs376203503	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702634	CCTGGTGTCCACAGA[A/G]CATGCCCATGCTCTG	63891
rs376364940	snp	C/T	0.000200103	0.0100006	intron-variant	RNF123	GRCh38.p7	3:49701485	CCCTGCCTTGACACC[C/T]GCCAGCTTCGACGTG	63891
rs376417230	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49698458	GGGGTTGGAGATACA[C/T]ACAACTCCTATGCCT	63891
rs376458254	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49692633	AAGCCCTATACTACC[C/G]TTCCAAGCCTCTGGT	63891
rs376470918	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49702681	GTCTGCTTCTTACAC[C/T]GGCTGATCTCTGCCC	63891
rs376474937	snp	C/G	0.000179449	0.00947061	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49720523	TAGGAGAGAGCAAGC[C/G]ACATCAGTGCTCCTG	63891
rs376480604	snp	C/T	0.000452167	0.0150293	intron-variant	RNF123	GRCh38.p7	3:49697235	AGGGTATGTGGCCAC[C/T]TCTGGAGTGGGGTTG	63891
rs376506314	snp	A/G			missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49699725	CGGGGCCAGCCCACC[A/G]TCCTCCTCACACTGG	63891
rs376549022	snp	A/T	0.000170445	0.00923003	intron-variant	RNF123	GRCh38.p7	3:49697315	AGGACACCCTATGCA[A/T]CCTGTCAAATGCTCC	63891
rs376565252	snp	A/C			intron-variant	RNF123	GRCh38.p7	3:49704338	TCCTGGGAAACAAAG[A/C]CAGGGACCAGCAGGA	63891
rs376596236	snp	A/G	0.000153988	0.00877328	intron-variant	RNF123, AMIGO3	GRCh38.p7	3:49716519	GTGGGAGTTGGGTGT[A/G]TCTGGTGAGGAGGGG	63891
rs376599465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49695048	ACTGCCCACAGATAT[A/G]TGCAGTCTGCTCTCA	63891
rs376622853	snp	C/T	3.36287e-05	0.00410039	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719282	CGAGGTCCGCAGTAG[C/T]GGCAGGTAACTCGGC	63891
rs376631445	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, upstream-variant-2KB	RNF123, MST1	GRCh38.p7	3:49691478	CGCATCTTTTCCTCT[C/T]CTGAACATGCACCCC	63891
rs376634099	snp	C/G/T	3.29735e-05	0.00406028	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49712571	CTTTGCCTTCATGCC[C/G/T]GAGTTCTACCTGAGC	63891
rs376635007	snp	A/G	0.000437904	0.0147905	intron-variant	RNF123	GRCh38.p7	3:49702022	TGGTGGTGGAGCCCT[A/G]GCCCAAACCTGCCCC	63891
rs376660864	snp	C/T	2.15473e-05	0.00328225	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713572	CACTTTGCCGACGCA[C/T]GCATTGTGGGCACTG	63891
rs376679342	snp	A/G	0.000823615	0.0202763	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49706049	CAGAGGACAAGCTCC[A/G]CCGGTGCCCCAAGAG	63891
rs376685153	snp	A/G/T	6.6427e-05	0.0057628	intron-variant	RNF123	GRCh38.p7	3:49698555	CCCTGTGGGTCATCC[A/G/T]CCCCATGACTGTTAC	63891
rs376736320	snp	A/T	0.000153988	0.00877328	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718441	GCATGCTGCTCCTGT[A/T]CGTTGCCTATGGCCA	63891
rs376781574	snp	G/T	3.29783e-05	0.00406055	downstream-variant-500B, intron-variant, upstream-variant-2KB	GMPPB, RNF123, AMIGO3	GRCh38.p7	3:49721161	GTACATGCAGGGCAG[G/T]CCTCATCCCCTCCCC	63891
rs376893628	snp	C/T	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720494	TTCTGACTGCCCTTG[C/T]ACCCTCCCCTACCTA	63891
rs376897957	snp	A/G	4.97814e-05	0.00498881	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720975	ACGGACATCCACATA[A/G]CCAGGCATCCAACTC	63891
rs376922086	snp	A/G	2.77127e-05	0.00372231	splice-acceptor-variant	RNF123	GRCh38.p7	3:49704649	CTGCTCTTCCTCCCA[A/G]ATGACCTTGCTTCCA	63891
rs376946347	snp	A/C	0.000153988	0.00877328	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49718766	GGCCCCGCTGGTGCC[A/C]GCGCTGTAGCAGGTG	63891
rs376960690	snp	A/G	3.29761e-05	0.00406041	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720912	GAGTGGGAACACGGT[A/G]CACAGGTCCATGCCA	63891
rs376984502	snp	A/G	0.000155988	0.00883004	intron-variant	RNF123	GRCh38.p7	3:49701919	ATCGAAGGTCAGCCC[A/G]CCTTGGGCACGGGGT	63891
rs377011567	snp	A/G	0.000139053	0.0083371	intron-variant, nc-transcript-variant	RNF123	GRCh38.p7	3:49712892	GACAAGATGGAACAC[A/G]GTGGGTGTAGACCTC	63891
rs377063915	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49693518	CAAACCACCACACCC[A/G]GTTAATTTTGGTATT	63891
rs377076534	snp	A/G/T	0.000235747	0.0108548	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717933	GGTGGGGGCCTGGGT[A/G/T]GGGGAGCCCTGGGCA	63891
rs377106838	snp	A/G	5.05055e-05	0.00502496	intron-variant	RNF123	GRCh38.p7	3:49715556	GTCCCTGATGATGCC[A/G]CCTCCTGTCCCCCTG	63891
rs377114100	snp	A/T	0.000415769	0.0144122	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687344	CCCAGGCCGGGACGG[A/T]GGGAAGGTGTTTGTC	63891
rs377154911	snp	A/T			intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720261	GTGGAGGTTGCAGTG[A/T]GCCGAGATCGTGCCA	63891
rs377254073	snp	A/G	0.000146732	0.00856413	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705111	GCCTCATGACCCCAC[A/G]GCGGCCTCTGAGCAC	63891
rs377265906	snp	A/G	1.65562e-05	0.00287712	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719051	GGTTATTGAACAGAA[A/G]CAGCTTCTCCAGCGC	63891
rs377285213	snp	C/T	0.000116572	0.00763365	intron-variant	RNF123	GRCh38.p7	3:49698143	CAACCAGGAGGTACA[C/T]GTTGGGGAGGGGACC	63891
rs377456141	snp	C/T	6.61737e-05	0.00575174	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49713986	AACTGGATCCTGGTG[C/T]GGCTCTGGAGGGTAA	63891
rs377503467	snp	A/G	0.00119737	0.0244387	intron-variant	RNF123	GRCh38.p7	3:49692436	CGTAATAATCACATC[A/G]TGGTAAATGGGGTAT	63891
rs377522558	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49708390	CCTGTCCTCCCTTCC[C/T]CAGCTTCCCTGACAG	63891
rs377555174	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF123	GRCh38.p7	3:49710573	GCTTCAGCAACCGCG[A/C/T]CTGGCCATATCCTAT	63891
rs377611075	snp	A/G	0.000927047	0.0215096	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49705158	GTCCGCACGCTGAGC[A/G]TGGAGCAGAGGACCC	63891
rs377639906	snp	A/C/T	0.000181761	0.0095315	intron-variant	RNF123	GRCh38.p7	3:49715806	ACCACTGCATGCCCA[A/C/T]GTGTTGGTGGCTCAG	63891
rs377644714	snp	C/T	9.93443e-05	0.00704715	missense, upstream-variant-2KB, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49687591	CAGCGCCCAGAACGC[C/T]GCAGCCTCGTGTGGG	63891
rs377689362	snp	C/T	1.65004e-05	0.00287227	intron-variant	RNF123	GRCh38.p7	3:49700399	GCTGTCAGTCTTCAC[C/T]GGGGTCGGGAAGATA	63891
rs377690361	snp	C/T	6.61026e-05	0.00574865	synonymous-codon, intron-variant, nc-transcript-variant	RNF123, AMIGO3	GRCh38.p7	3:49716403	CTCAGGCCTAGAGAG[C/T]GTGGACCACTATCCC	63891
rs377691477	snp	C/T	0.000831124	0.0203684	intron-variant	RNF123	GRCh38.p7	3:49704645	CCTCCTGCTCTTCCT[C/T]CCAGATGACCTTGCT	63891
rs377714575	snp	A/G	0.000188058	0.00969504	intron-variant	RNF123	GRCh38.p7	3:49713734	GCACGGTGTGTCCCC[A/G]CAGACATCCGAGACT	63891
rs377740163	snp	A/G	3.32071e-05	0.00407461	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49687503	AGAGACAGAAGATCA[A/G]CTTGGGCTGAGGTCC	63891
rs397509422	snp	C/T	0.000148867	0.00862621	GMPPB, RNF123	3	allele_origin=T(germline)/C(germline)	3:49721835	TGAGGTAGAGCTCAT[C/T]ATTAACTATGACGTC	63891
rs397703513	in-del	-/C	0.375	0.216506	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688001	GGTCCATCCCAGAAG[-/C]CTTGTAGCTTTGATC	63891
rs397739513	in-del	-/A	0	0	intron-variant	RNF123	GRCh38.p7	3:49712229	CAAAAAAAAAAAAAA[-/A]CTTGCTTACAAATAT	63891
rs397874489	in-del	-/T			intron-variant	RNF123	GRCh38.p7	3:49693350	AGTGTGCCTGGCCTT[-/T]TTTTTTTTTTTTTTT	63891
rs397989558	in-del	-/A	0	0	intron-variant	RNF123	GRCh38.p7	3:49693373	GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	63891
rs398105858	in-del	-/C			intron-variant	RNF123	GRCh38.p7	3:49708513	GGCTCACAGACCCCC[-/C]AGCTGGGCCTTACTT	63891
rs527244878	snp	A/T			intron-variant	RNF123	GRCh38.p7	3:49704479	GGGCCCTTGAGATGC[A/T]GAGTGAAGGCTGGGT	63891
rs527254009	snp	A/G	0.000399281	0.0141238	intron-variant, missense	RNF123, AMIGO3	GRCh38.p7	3:49719219	GCAGCTGGAAGAGGG[A/G]CGCCAACCAGCCGGG	63891
rs527415145	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49704322	CCTGGAGAGCAGGAA[G/T]TCCTGGGAAACAAAG	63891
rs527502058	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49716297	GGTGCTCTGCAGTCT[C/G/T]GGCTCACCCTTCTGT	63891
rs527528541	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49688882	AAGGTTTGGTGGGGA[C/T]ACTTGAGGTGCCCTG	63891
rs527826548	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF123, AMIGO3	GRCh38.p7	3:49720040	GGTACCCCAGGCCGG[A/G]CGCGGTGGCTCACGC	63891
rs527838769	snp	C/G	5.01886e-05	0.00500917	intron-variant	RNF123	GRCh38.p7	3:49698390	ATTGGTGGGCTCTGG[C/G]CCAGACCCTGCCTGC	63891
rs527967674	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	MST1, RNF123	GRCh38.p7	3:49690700	CAGACCAGTGGTGGT[C/G]TGCACTTGGGGGAAT	63891
rs528256688	snp	C/T	1.65888e-05	0.00287996	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49701527	CGTCTTCTTTTACAT[C/T]AAGAGCCCCCTGCGT	63891
rs528361243	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49694260	GTGTACAATTTGATA[A/G]GTGTTAACATATATA	63891
rs528403324	snp	C/G	2.01286e-05	0.00317237	intron-variant	RNF123	GRCh38.p7	3:49702039	CCCAAACCTGCCCCC[C/G]ATCTCCTGGAGCCTG	63891
rs528435216	snp	C/T	0.000203739	0.010091	missense, nc-transcript-variant	RNF123	GRCh38.p7	3:49703439	CAGAGGCCTACATCC[C/T]GCCCCAGGTCTTCTA	63891
rs528599140	snp	C/T	0.00159617	0.0282053	intron-variant	RNF123	GRCh38.p7	3:49696505	AGGCACATGCCACCG[C/T]GCCCAGCATTTTTAG	63891
rs528634640	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	RNF123, AMIGO3	GRCh38.p7	3:49717004	TATGAAGCCAGGGTA[C/T]CGCCTCAGCCATTAG	63891
rs528679262	snp	C/G			intron-variant	RNF123	GRCh38.p7	3:49699325	GGAATGTGAAGCATC[C/G]TCCCTAGGGAGAATA	63891
rs528758272	snp	A/C	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49710737	TTCTTTTTCATGCTT[A/C]GTTGCTCTGGCTGGG	63891
rs528795123	snp	A/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49709964	TGCATGAGGGTTCCA[A/G]TTTCTCCATACATAT	63891
rs528821053	snp	A/G			intron-variant	RNF123	GRCh38.p7	3:49703821	TTCAGGGATGAGCAC[A/G]AGCTGCCCCGGTGCA	63891
rs529197399	snp	C/T	0.00199481	0.0315187	intron-variant	RNF123	GRCh38.p7	3:49695398	AGCCACCATGCTTGG[C/T]CTGTAACTGCTTTTG	63891
rs529249180	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MST1, RNF123	GRCh38.p7	3:49688290	CTCCAAATCTGGGCT[C/T]TCACCTGCACAAAGG	63891
rs529392117	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant	MST1, RNF123	GRCh38.p7	3:49689141	GGCGGCAGAGCCCAG[A/G]GAGGCTCGCTCATCT	63891
rs529620090	snp	C/G	0.00835141	0.0640778	intron-variant	RNF123	GRCh38.p7	3:49691671	AGAGAGTCTGCCTTC[C/G]GTACTCTGCTTCTTC	63891
rs529808427	snp	C/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49714264	ACTCTCCACTTCTTC[C/T]AGCCCCTCTCTGGTT	63891
rs529817046	snp	G/T	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49692505	TCTAGTTATACTCTT[G/T]TAGTTATTTTTAAAT	63891
rs529846709	snp	C/T	0.000125652	0.00792528	synonymous-codon, nc-transcript-variant	RNF123	GRCh38.p7	3:49713775	GGCCCTGGCCAGCTA[C/T]GTGTGCTACCCACAC	63891
rs529848791	snp	C/T			intron-variant	RNF123	GRCh38.p7	3:49710428	GGGACTATAGGCATA[C/T]GCCACCACGCCCGGC	63891
rs529945071	snp	C/G	0.000399281	0.0141238	intron-variant	RNF123	GRCh38.p7	3:49699925	CCCTCAGACCTCAGT[C/G]AGTCCCCTAGGGAAA	63891

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