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

RNFT2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs116551905	snp	C/T	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116808943	ATGGTCACTGTCTGG[C/T]GAGCTGGCCTGGCTC	84900
rs116615448	snp	A/G	0.0310518	0.120672	intron-variant	RNFT2	GRCh38.p7	12:116797454	AATCCCAGTACTTGG[A/G]AGACTGAGGCAGGAG	84900
rs116645516	snp	A/G	0.0471551	0.14613	intron-variant	RNFT2	GRCh38.p7	12:116811687	GGCATGCGTGCGCGT[A/G]CGTTTGTGCATGTGT	84900
rs116645620	snp	A/G	0.021333	0.101051	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852551	AATGGGGCCATGTGA[A/G]TGCAGCTGCTCTGTT	84900
rs116669686	snp	A/G	0.0883596	0.190715	intron-variant	RNFT2	GRCh38.p7	12:116747624	TCCTGCTGCCATTTC[A/G]GACTGAATAACATCT	84900
rs116673785	snp	C/T	0.10237	0.201756	intron-variant	RNFT2	GRCh38.p7	12:116795484	CTGCGCTGTCTAATA[C/T]AGTAGCTACAGGCCA	84900
rs116754010	snp	C/T	0.128359	0.218411	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750114	CCATTTCCACCATGG[C/T]GGCCACCGCGGGGGC	84900
rs116755370	snp	G/T	0.0368353	0.130617	intron-variant	RNFT2	GRCh38.p7	12:116760495	CTGCTGGGGGACCCA[G/T]TGAGCTCCCAGGGCC	84900
rs116782168	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845878	TTCCTATCTCAGGAG[C/G]TTTGCACAGGAGACT	84900
rs116858769	snp	A/C	0.0640965	0.167152	intron-variant	RNFT2	GRCh38.p7	12:116763195	AAAAAAAAAAATCTC[A/C]TCAGAAAGTGGCCTA	84900
rs116966306	snp	A/G	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116800171	ACAGTCTGCAGAACC[A/G]TGAGCCAAGATAAAC	84900
rs116982685	snp	A/G	0.0287284	0.116357	intron-variant	RNFT2	GRCh38.p7	12:116752079	TATCGGTCAGGTGTG[A/G]TGGCTCATGCCTATA	84900
rs116992776	snp	A/T	0.0333695	0.124785	intron-variant	RNFT2	GRCh38.p7	12:116767180	ATAATTGATTTTATT[A/T]AACCCAGTATATCAA	84900
rs116993723	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116845826	CCTGCACCCCCAACT[A/C]CAGCCACATCAGCTA	84900
rs116996945	snp	A/G	0.0236746	0.106192	intron-variant	RNFT2	GRCh38.p7	12:116843426	GAGCCCCAAAAGGTC[A/G]AGGCTGCAGTGAGCC	84900
rs117028867	snp	C/T	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116821319	CCCCTCCTGGCCGGG[C/T]GCTGCTGTGAAGTCA	84900
rs117059383	snp	C/T	0.0107246	0.0724382	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736449	GGGACTTACAACACT[C/T]AGCCTCTCTGTTTGC	84900
rs117062015	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116814067	CCTTGGAAAACATGA[C/T]CCCAGCCCTCCCCGT	84900
rs117118360	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738516	CGAAGTGCACCTGCC[A/G]GCTTCCAGTCCAAGT	84900
rs117158709	snp	C/T	0.10237	0.201756	intron-variant	RNFT2	GRCh38.p7	12:116812893	TTTCAGTACCTTGTC[C/T]ATAATCCCACGCCAT	84900
rs117172750	snp	C/T	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116816447	CACCAGAGGCGATCG[C/T]GGCCTCCTCCTCCCC	84900
rs117204594	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116780317	GGTGGGGATGGTTTC[A/G]GAATGAAACTGTTCC	84900
rs117218966	snp	A/C	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116799987	GGTGATGAGTGAGTT[A/C]TTGCTATATTAGTTC	84900
rs117250218	snp	G/T	0.0256215	0.110247	intron-variant	RNFT2	GRCh38.p7	12:116784493	TGGTACGAAAAAACA[G/T]GGCTGCCTAGGGAGG	84900
rs117263506	snp	A/T	0.0839998	0.186933	intron-variant	RNFT2	GRCh38.p7	12:116817633	TTGTCACTACTGTAG[A/T]ACACTTAAGAATTAA	84900
rs117351358	snp	C/T	0.0256215	0.110247	intron-variant	RNFT2	GRCh38.p7	12:116783187	TCAGAGATCCCCTCA[C/T]AGACACTTGTCAGAA	84900
rs117360286	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826956	GGCTGGGTGTGGTGA[A/G]TCATACCTGTAAACA	84900
rs117392636	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737542	AGGAGGAGGAAGGTG[A/G]GGAAGGTAAGGAAGG	84900
rs117411656	snp	A/G	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116767552	TTTCAACATACGATC[A/G]ATATAAAAATTATGT	84900
rs117471462	snp	A/C	0.0839998	0.186933	intron-variant	RNFT2	GRCh38.p7	12:116816643	AATCCCACCTCTGCT[A/C]CATCTGAGCTCTATA	84900
rs117581426	snp	A/C	0.0558544	0.157504	intron-variant	RNFT2	GRCh38.p7	12:116803707	GAATGAAATCACCAT[A/C]CCCCAGGATGTTCTC	84900
rs117584086	snp	C/T	0.13875	0.223883	intron-variant	RNFT2	GRCh38.p7	12:116849826	TGTTTCCCTCCCTCC[C/T]TCCTTCCTTCCTTCC	84900
rs117593718	snp	A/C	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116776487	CTCCCTGTATTATGA[A/C]CTGGATGACCACTCC	84900
rs117600660	snp	C/G	0.0352966	0.128072	intron-variant	RNFT2	GRCh38.p7	12:116839486	GTGAATGATGGACAG[C/G]TGGAGAAGTTGGTGG	84900
rs117717302	snp	A/G	0.00953873	0.0683987	intron-variant	RNFT2	GRCh38.p7	12:116805005	TTTACACTTCTTCCA[A/G]TGCTGGATACAAGTT	84900
rs117727938	snp	G/T	0.0221141	0.102801	intron-variant	RNFT2	GRCh38.p7	12:116753100	ATTGAACATTAAACT[G/T]GAATTCCTTATGGCG	84900
rs117734151	snp	C/T	0.0279526	0.114869	intron-variant	RNFT2	GRCh38.p7	12:116829376	CCAGAGGGAAACCAG[C/T]ATTTCCCTCCAGGGG	84900
rs117735574	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116781279	GCTCTCTGCCCAGGG[C/G/T]GCTGACCTGCGCGAA	84900
rs117805802	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738249	GCCGGACCCGGCGAC[G/T]CCAAGAAACCACCCA	84900
rs117811162	snp	C/T	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116780330	TCGGAATGAAACTGT[C/T]CCACTTCAGATCATC	84900
rs117865006	snp	A/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116837628	TTTGCATGAATCAAC[A/G]TTCAAAAAGAAGACT	84900
rs117866060	snp	A/G	0.0163485	0.0889211	intron-variant	RNFT2	GRCh38.p7	12:116851780	AGGGAGGGAGGGAGG[A/G]AGGAAGGAAGGAAGG	84900
rs117893408	snp	A/G	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116825678	GAAATTGGCAAACAC[A/G]CAAATCAGGGCCTTT	84900
rs117902853	snp	A/G	0.0399052	0.1355	intron-variant	RNFT2	GRCh38.p7	12:116811679	ACGCACCCGGCATGC[A/G]TGCGCGTGCGTTTGT	84900
rs117918140	snp	A/G	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116827335	AGGCTTTTCATAGGC[A/G]GTGACAGTTAGCTGA	84900
rs117921747	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737541	AAGGAGGAGGAAGGT[A/G]AGGAAGGTAAGGAAG	84900
rs117958367	snp	C/T	0.0236746	0.106192	intron-variant	RNFT2	GRCh38.p7	12:116792846	GCTGGGCCTCCGCAC[C/T]ATCCACTGAGAAGGT	84900
rs117968796	snp	A/G	0.0240643	0.107019	intron-variant	RNFT2	GRCh38.p7	12:116814694	TTTTTTTTTTTTTCC[A/G]ACAGAGTCTCACTCT	84900
rs117970574	snp	C/T	0.0217236	0.101931	intron-variant	RNFT2	GRCh38.p7	12:116815395	CCAAAATCTGTGTCA[C/T]TGGGCTAAAGCCAAG	84900
rs118009373	snp	C/T	0.0240643	0.107019	intron-variant	RNFT2	GRCh38.p7	12:116765418	TGCATCATAACAGTG[C/T]GTGGGGCACTGAGCT	84900
rs118010498	snp	C/T	0.0267878	0.112589	intron-variant	RNFT2	GRCh38.p7	12:116777700	TCATCACTGCTGCAC[C/T]GCAGGGTCTGTAATC	84900
rs118025463	snp	A/G	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116797893	GGTCACTGGGTGATG[A/G]TCATGGAAAGCGGTG	84900
rs118056840	snp	A/C	0.078151	0.181571	intron-variant	RNFT2	GRCh38.p7	12:116763899	GAAAAAAATACTTAC[A/C]TACTCATGTTTATAG	84900
rs118077904	snp	C/T	0.030278	0.119257	intron-variant	RNFT2	GRCh38.p7	12:116781498	GGAGTCCAAAGTGGG[C/T]TTTACTGCGGTGAAA	84900
rs137892384	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116850565	CCTCCCAGATAGCCC[A/G]GGCCTGCAGATTAGA	84900
rs137906145	in-del	-/GGGGGGGGG			intron-variant	RNFT2	GRCh38.p7	12:116820479	GTTACTGGATTGGCT[-/GGGGGGGGG]GTGGTGGATATGGAA	84900
rs137919437	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769283	GAATTGCTTGGACCC[A/G]GGAGGCAGAGGTTGC	84900
rs137928156	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833103	TTTGTATTTTTAGTA[A/G]AGTTGGGGGTTCGCC	84900
rs137999253	snp	A/C	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116797816	TTATACCTACTTTTA[A/C]TTACATGTAGATTAA	84900
rs138002666	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116825937	ATGTGTATAAAAGAG[A/G]TTCGTAAACAGGCAA	84900
rs138004465	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116743720	ATCCCATACCCCCTG[C/T]GACTCTGGGGTTGGC	84900
rs138012202	snp	A/G	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116766091	AGCCTGAGCCAAATA[A/G]CAAGACTCTGTCTCT	84900
rs138027941	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116823912	CCCCATTTTACTAGC[A/G]AGGAAACTGAGGCAC	84900
rs138037560	snp	C/T	0.0115144	0.0749975	intron-variant	RNFT2	GRCh38.p7	12:116786811	GTCAGCGGGGCTGCA[C/T]TGCCTCCGGAGGCTC	84900
rs138060669	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116801378	ATTCTAGAGCATGTA[A/G]CAAGAAAAGCAAGTA	84900
rs138101207	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116796989	GGGGTGTGCTACTGG[C/T]ATTTAGTGGACAGAG	84900
rs138109145	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739574	CCTCTGGGAAGAGAC[A/G]ACATTTGCCCTGCGG	84900
rs138109695	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853120	GTCCTAGGGAAAACA[A/G]TGTCTGATGAGGAGT	84900
rs138110309	snp	C/T	0.0154538	0.0865337	intron-variant	RNFT2	GRCh38.p7	12:116820059	TAAGACTTTGAAATT[C/T]CTTGTTTCTTTTGCT	84900
rs138132289	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116847298	AAGTGCCCTTTATAG[C/T]TGGCATTTTTTTTGC	84900
rs138152399	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116784293	GTGGTAGGCAGCATC[C/T]GCCGCACGTGTCGTG	84900
rs138264117	in-del	-/CAGCAGGA	0.0460142	0.144533	intron-variant	RNFT2	GRCh38.p7	12:116815860	GCAAAGTCACCCTCC[-/CAGCAGGA]CAGATCCACACTTGA	84900
rs138273117	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837384	TTCATGCAGTGTCTC[A/G]GGGGACTGAGGCAGA	84900
rs138326059	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116775330	CTTACTGAAGTCACC[A/T]GAAGTCACCAGTCTA	84900
rs138352922	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756756	TAAGGATTTTAGCAT[C/G]TATGTTCATCAAGGA	84900
rs138375516	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116849633	TCCTCTCTCGTTCTG[C/T]GGTATAGTGCGTGCC	84900
rs138384456	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116743245	AAAAAAAAAAAAAAA[A/C]CGGTTAAAAAACACT	84900
rs138416651	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748923	TCTTTATCTGTAAAG[C/T]GGGAATATCAGTAGG	84900
rs138423033	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116780731	CAACAGGCCTAGGGA[A/G]GTCCTAAGATGCCTC	84900
rs138424357	snp	A/G	0.0596104	0.162024	intron-variant	RNFT2	GRCh38.p7	12:116805464	AGGAGCTGATGCTGC[A/G]TTTTTTGTTGTTGTT	84900
rs138431200	in-del	-/AAA			intron-variant	RNFT2	GRCh38.p7	12:116832131	GCAAGACCTTGTCTC[-/AAA]AAAAAAAAAAAAAAA	84900
rs138437463	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116815915	TTTGAAGTCATGGGC[C/T]CCAGACCACCAGGAA	84900
rs138470562	snp	A/C	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116808608	CGCCTGGCTCCACAC[A/C]CCCCAAGCTGTTGTT	84900
rs138503525	snp	A/G	0.0244538	0.107838	intron-variant	RNFT2	GRCh38.p7	12:116777202	GGATTACAGTCGTGA[A/G]CCACCGTGCCCAGCC	84900
rs138521237	in-del	-/TTTG	0.382208	0.212182	intron-variant	RNFT2	GRCh38.p7	12:116842569	TATTTTATTTATTTA[-/TTTG]TTTGTTTGTTTGTTT	84900
rs138587979	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116816448	ACCAGAGGCGATCGC[A/G]GCCTCCTCCTCCCCC	84900
rs138627477	snp	G/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116801084	AACACTCTGAGAAGG[G/T]AGGTGCTGTTATTGT	84900
rs138653629	snp	C/T	1.64787e-05	0.00287038	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754053	TTCGAGAACAGGTCT[C/T]ACTGAAGGTGAGTCA	84900
rs138665171	snp	A/G	0.0372196	0.131242	intron-variant	RNFT2	GRCh38.p7	12:116769082	AAATAAAAGTTGGCC[A/G]GGCGCAGTGGCTCAC	84900
rs138670235	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850082	ACTCTTGACCTCAAA[C/T]GATCAGCTCGCCTCA	84900
rs138680311	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116792736	ATCCTCATCAATCCT[C/T]GTCTGTGGAGAAGAA	84900
rs138704289	snp	G/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116769814	AGGTGGGTGGATCAT[G/T]TGAGGTCAGGAGTTT	84900
rs138713511	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116828095	ATGAGACCAGGCAGA[C/T]GAAGCAGGAGGCTGC	84900
rs138742377	in-del	-/TGGAGTGCA			intron-variant	RNFT2	GRCh38.p7	12:116821890	CTCTGTCGCCCAGGC[-/TGGAGTGCA]TGGAGTGCATGGAGT	84900
rs138751697	snp	A/G	0.0607341	0.163335	intron-variant	RNFT2	GRCh38.p7	12:116773003	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA	84900
rs138771298	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116830853	AGGTTGCAGCGAGCT[A/G]AGATTGTGCCACTGC	84900
rs138783168	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827576	GCTACAGGCCAAATA[A/C]GTCCTGCCACTTGTT	84900
rs138784956	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116790334	TTCTAAACTCTGAGG[A/G]TACATCAGTGAACCA	84900
rs138823913	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835162	GCCCCCATTATTCCC[A/G]TTTTACAGGTTAAGA	84900
rs138847778	in-del	-/GAGGAAGGT			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737532	GGAGGAAGGAAGGAG[-/GAGGAAGGT]GAGGAAGGTAAGGAA	84900
rs138901309	snp	C/T	0.00755907	0.0610114	intron-variant	RNFT2	GRCh38.p7	12:116743413	TTGGGACCATAGGCA[C/T]GCACCACCACGTTTG	84900
rs138926826	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116781507	AGTGGGTTTTACTGC[A/G]GTGAAAACAGAAGTT	84900
rs138952218	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116752064	CTTTCCATGAGAAAA[C/T]ATCGGTCAGGTGTGG	84900
rs138966445	in-del	-/T	0.0256215	0.110247	intron-variant	RNFT2	GRCh38.p7	12:116838457	ACACAGTTTTGACAG[-/T]TATTGCTAAACTGCC	84900
rs138967408	snp	C/T	0.145642	0.227177	intron-variant	RNFT2	GRCh38.p7	12:116808031	TGGAGGGCAATGGCA[C/T]GATCTCACTACAACC	84900
rs139006872	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116838385	CATCCCATTTCACAC[A/G]CACATGAGCTCTTGG	84900
rs139021369	snp	C/T	0.0287284	0.116357	intron-variant	RNFT2	GRCh38.p7	12:116756054	TTATGTGGGCTCTTT[C/T]CTGGTTCCATATGAA	84900
rs139041103	snp	A/C	0.122411	0.214991	intron-variant	RNFT2	GRCh38.p7	12:116841623	CATGGTGGCACACAC[A/C]TGTAGTCCCAGCTAC	84900
rs139047008	in-del	-/AGAGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116845275	TATATATATATATAT[-/AGAGAGAG]AGAGAGAGAGAGAGC	84900
rs139050116	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813610	TGTCTCCCCCATTAG[A/G]ACTTAAAACTTGGCA	84900
rs139050345	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116848090	TTATGAGTGAGAACA[C/T]GTGGTGTTTGGTTTT	84900
rs139087667	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789956	ATGGATGGTGGATGG[A/G]TGGGTGGATGGATGG	84900
rs139096669	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116790834	TGGTGGCACTCACCT[G/T]TAGTCCCAGCTACTT	84900
rs139104136	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116784463	AACTGTTGCCAAGGA[A/G]GAGGCAATGTCAGCT	84900
rs139119687	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116842776	ACGGGGTTTCGCCAT[G/T]TTAGCCAGGCTAGTC	84900
rs139168434	snp	A/C	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116786575	GGCGCCTTCTGGGTT[A/C]TGTCTAGATTCTTTC	84900
rs139190298	snp	A/G	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116782184	CAAGGATGACACACA[A/G]ATTCATGAAGCATTC	84900
rs139196870	snp	A/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116845209	TGATCGCACCACTGC[A/T]CTCAAGCCTGGATGA	84900
rs139242977	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116787421	CTGTAAAGGTAAAAA[A/G]ACTTGACAGGGCACA	84900
rs139294758	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116835794	GGCAACAAGACAAAA[A/G]CCATGCAACACTGTT	84900
rs139298742	snp	C/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116778498	GAAAAATAGGCCTCA[C/G]CAGAAGCTAGTGCCA	84900
rs139305837	in-del	-/AAAAA			intron-variant	RNFT2	GRCh38.p7	12:116806378	GAGTGAGACTGTCTC[-/AAAAA]AAAAAAAAAATATAT	84900
rs139321200	snp	C/T	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116745882	TATGGTCTTTGACCT[C/T]GTGGAGTGGAGCTCT	84900
rs139322662	snp	G/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116758394	ACTTTGGTTTTTTCA[G/T]TTTTTGTTTTTGCTT	84900
rs139342998	in-del	-/AAC	0.0471551	0.14613	intron-variant	RNFT2	GRCh38.p7	12:116816837	ATAAAAACAAAAAAT[-/AAC]AAATACTCGTGTACC	84900
rs139369953	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787741	AAAAAAAAGATATAA[C/T]GTGTATAATGTGTGT	84900
rs139371729	snp	A/T	0.000451467	0.0150176	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766886	CTCTATGTGCTTTAT[A/T]CATTCAGCTCCCAGC	84900
rs139373884	snp	A/T	0.0923359	0.194016	intron-variant	RNFT2	GRCh38.p7	12:116759414	TGAACTAGTGTGATT[A/T]TGGGGGAGTGTTGAA	84900
rs139400012	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116831574	AATGCTGTAGTGACC[A/G]TTCCTATAGGCACAT	84900
rs139436315	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116740706	TCAACCCAGAATCCA[C/T]GTCTCCTGCCAGTCC	84900
rs139466630	snp	G/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116764062	GCAGCAACCTGGATG[G/T]GATTGGAGACTATTA	84900
rs139469766	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116844851	TCTTTTGTCCAGGGT[A/G]GCATAGTTAAGTCCC	84900
rs139516549	snp	A/C	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116770394	TAACTAGTTTTGTGT[A/C]AGTCAACTCTGTGGT	84900
rs139611270	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116810716	AATGATTAAGCAAGG[C/T]AGCCAGGCTCCCTGA	84900
rs139615772	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116753488	TTTATCACAAATTCT[A/G]TCTGATTCTATCAAT	84900
rs139624416	snp	C/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116843758	CCAGATTCTGTCCTC[C/G]CATTTCTCTGAGGAA	84900
rs139645560	snp	A/G	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116802821	ACAGGTGGGCCTGGC[A/G]CAGTGGCTCATGCCT	84900
rs139684138	snp	A/G	0.02016	0.0983543	intron-variant	RNFT2	GRCh38.p7	12:116753403	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	84900
rs139688365	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810142	GACCAGGAGTTTCAC[G/T]CTGAAAGCTCACAGT	84900
rs139738896	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774474	GATCACTGCATAAGC[A/G]AATGCTAATCAGAAC	84900
rs139756940	snp	A/G	0.0275645	0.114116	intron-variant	RNFT2	GRCh38.p7	12:116806237	TAGCCAGGCATGGTG[A/G]TGCATGCCTGTAATC	84900
rs139793020	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116817083	AGTGGTGCGATCGCA[G/T]CTCACCGCAACCTCC	84900
rs139821913	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774729	GCGTCAACACAGATC[C/T]CATACGCCGCATTCA	84900
rs139824657	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116820469	TGTGACCAGTGGTTA[C/T]TGGATTGGCTGTGGT	84900
rs139825617	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116785666	GCACTGGGCAGAGCT[C/T]TGTAAACGGTGAGTA	84900
rs139834463	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116851298	TTCAAACTCCTGGGC[C/T]CAAGTGATCCTCCCT	84900
rs139865313	snp	A/C	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116814249	TTCTGTACCAGGCCC[A/C]GGACTAGGTCCCAGA	84900
rs139900012	snp	A/G	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116817495	GCTGTTATTAAAGGT[A/G]AGAGCATAAGCTGTA	84900
rs139947917	in-del	-/GAAA	0.314268	0.241598	intron-variant	RNFT2	GRCh38.p7	12:116851795	AAGGAAGGAAGGAAG[-/GAAA]GAAAGAAAGGTCAGC	84900
rs139964408	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116787078	TGATTATTTTCTAAA[C/T]AATGTCACATTCACA	84900
rs140002109	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832592	GACTGGAATTTCTGG[A/G]TCATAAAGTAGGTAT	84900
rs140038761	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116822428	TTCCTACTAGATACT[A/G]TCAGATCCAGCATTT	84900
rs140049731	snp	C/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116776371	TCATGATCATGGAAG[C/G]ACTGGAGATTTGGCA	84900
rs140072696	snp	C/T	6.59055e-05	0.00574007	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835978	TTCGACATCTGTGGA[C/T]GTGTGGGCGGAGTTA	84900
rs140076656	snp	C/G	0.0314385	0.121371	intron-variant	RNFT2	GRCh38.p7	12:116829502	ACAAAAATCAGGCAG[C/G]GGGTGAGTGATGATT	84900
rs140087125	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116767769	ATTTTTAGTAGAGAC[A/T]GGGTTTCACCATATT	84900
rs140160330	snp	C/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116744700	CACAGCCTCTGTCCC[C/G]CTAAGGAATATTCTT	84900
rs140173217	snp	A/G	0.0505692	0.150756	intron-variant	RNFT2	GRCh38.p7	12:116802074	TGATCCACCTGCCTT[A/G]GCCTCCCAAAGTGGT	84900
rs140178133	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116834868	TTTTTTTTTTTTTTT[-/T]AGACCGAGTCTCGCT	84900
rs140193025	snp	A/T	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116808019	TGTTGCCCAGGCTGG[A/T]GGGCAATGGCACGAT	84900
rs140247334	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116829740	ACGTGCCACCATACC[C/T]GGCTATTTTTTTGTA	84900
rs140257670	snp	A/C/G	0.0240643	0.107019	intron-variant	RNFT2	GRCh38.p7	12:116771340	TGGCGTGCACCTATA[A/C/G]TCCCCGCTACCCTGG	84900
rs140267506	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852469	CAAGCTCCGTTACTA[C/T]GGCGATGGCCATGAT	84900
rs140277175	snp	C/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116785910	AAAAAAAAATTGGCC[C/T]GATGTGGTGTACATG	84900
rs140299150	snp	A/C	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739322	AACTGGGAGACCCAT[A/C]GATGTTTTATTCATT	84900
rs140306985	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116754216	CAGTGAGAACGTACA[A/T]TGTTTGGTTTTCCAT	84900
rs140349345	snp	A/G	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116796851	TGGAATAAGAACTTC[A/G]AGAAGAGCCAGCCAC	84900
rs140449652	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737614	AGGAGGGGAGGTAGG[A/C]AGAAGGGAAGGAAGG	84900
rs140455398	snp	A/C	0.0360663	0.129354	intron-variant	RNFT2	GRCh38.p7	12:116792238	TATTTTTAGTAGAGA[A/C]GGGGTTTCACCATGT	84900
rs140462895	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116815442	TCCTTTGGGAGGCTC[C/T]GGGGGACAATCCATT	84900
rs140507978	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116781983	ACTCGGGAGGCTGAC[A/G]CAGGAGAATTGCTTA	84900
rs140589156	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116800267	ATTGGGAGGCCAGGG[C/T]GGGCAGATCATTTGA	84900
rs140591014	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116765376	GGTGGATGGAGATGC[A/G]TTTGTTTCGTCCACT	84900
rs140601788	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783825	ACAGATTGTCAACAA[C/T]GGATCATTTTTCTGC	84900
rs140631597	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768547	CCATCATAACGCTGT[A/G]GCACAGTGCCTTACT	84900
rs140638341	snp	C/T	0.0755793	0.179102	intron-variant	RNFT2	GRCh38.p7	12:116808049	TCTCACTACAACCTC[C/T]GCCTCCCAGGTTCAA	84900
rs140649861	snp	A/G	0.0162398	0.0886349	intron-variant	RNFT2	GRCh38.p7	12:116846409	CCTCCCAAGTAGCTG[A/G]GACGGCACATGCCAC	84900
rs140650442	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779024	GGTTAAAAGATCCAC[A/G]TGAGGTCACACAGCA	84900
rs140709252	in-del	-/TTCCCC	0.495016	0.0496707	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852377	CACCAAACCAGGACT[-/TTCCCC]TTCCCCTTGGCTTGG	84900
rs140710868	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116841640	GTAGTCCCAGCTACT[C/T]GGGAGTCTAGGGCAG	84900
rs140759713	snp	A/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116783179	ATTGAGGCTCAGAGA[A/T]CCCCTCATAGACACT	84900
rs140773304	snp	C/T	0.00914312	0.0669923	intron-variant	RNFT2	GRCh38.p7	12:116757838	TGTATCTGTTAAATC[C/T]ATTTGTTCCAAGGTA	84900
rs140773538	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837318	GAGACAGACACTTAC[A/T]TAAATAACTGTGAAG	84900
rs140776745	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780368	GGATTCTCATAGGGA[C/G]CATACAACCTAGATC	84900
rs140807046	snp	A/G	0.143284	0.226079	intron-variant	RNFT2	GRCh38.p7	12:116800526	TAATCCCAGCTACTC[A/G]GGTGGCTGAGGCAGG	84900
rs140840432	in-del	-/C	0.120326	0.21374	intron-variant	RNFT2	GRCh38.p7	12:116831785	TTCAATGAGTTTTGG[-/C]AAACGTGCGCACCCA	84900
rs140867669	snp	A/G	0.0298908	0.118541	intron-variant	RNFT2	GRCh38.p7	12:116753220	CAGTGGTGTGATCTC[A/G]ATTCACTGCAGCCTC	84900
rs140879826	snp	C/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116828420	CTTCTCTTAGACTTT[C/G]TTGATCAGTTTCCCC	84900
rs140880449	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116833296	AGCTAGGAAGGACAC[A/G]TATCTCCCCGCTTTG	84900
rs140881648	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116791807	AGAGAATTCTGGATC[A/G]TGCTGTAATCCTATG	84900
rs140902139	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742685	CAGTGACTCACGCCT[A/G]TAATCCCAACACTTT	84900
rs140909976	in-del	-/GA			intron-variant	RNFT2	GRCh38.p7	12:116774795	GTGGAGGGTGGAGGG[-/GA]TGGAGGGTGGAGGAG	84900
rs140937262	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738414	TTTCTCCCATCATGG[C/T]CTGTGTAGTCTCCTG	84900
rs140944670	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795020	AGGCAAATCCTCTGT[A/C]CCAGAAACATACATA	84900
rs140951991	snp	A/G/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116846639	TGTTTAGATTTTTTT[A/G/T]TTATTATTTCCTCAA	84900
rs140982073	snp	A/G	0.0275645	0.114116	intron-variant	RNFT2	GRCh38.p7	12:116824362	TACTGAGTCCCAAAC[A/G]CTTTCTATTAGTTAG	84900
rs140998819	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116826419	GCTCATAATCTGATC[A/G]TATTCCTTGTTCTCT	84900
rs141048998	snp	C/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116827205	AGCCTAGGCAACAGG[C/G]TGAGACTCCATCTCA	84900
rs141057496	snp	A/C	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116761273	TCTGCCTCAGTCTCC[A/C]CAGTAGCTGGGACTA	84900
rs141094564	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116833720	CATCACTGCCCGGGG[C/T]GGGGGGCCCCCCAGC	84900
rs141094684	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116811743	CTCATGACCCTCGTG[A/G]AAATCCAGGCCCTGT	84900
rs141129361	in-del	-/TTTGTTTTGT/TTTGTTTTGTTTTGTTTTGT	0.0387552	0.1337	intron-variant	RNFT2	GRCh38.p7	12:116785293	GGGGGGGGTTGTTTG[lengthTooLong]TTTGTTTTGTTTTGT	84900
rs141131766	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116743414	TGGGACCATAGGCAC[A/G]CACCACCACGTTTGG	84900
rs141162465	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116837076	TCTGTATAATTATTA[A/T]TACCATTTGTTTTTA	84900
rs141166203	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116801173	CAGCAAAGCCAGGGG[G/T]TGCTGAGCCCAGGGG	84900
rs141170097	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766753	CCAGTCATCAGGGTA[C/T]ATTCTGGAAGGTTCT	84900
rs141276499	snp	A/C	0.046775	0.145601	intron-variant	RNFT2	GRCh38.p7	12:116819393	CGGCGGCGCGCAGAG[A/C]GGGGCGGCCCGGGGC	84900
rs141288077	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770834	AAATGGCTCACAGGT[A/G]TGAGCCATTGTGACC	84900
rs141314072	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739206	CCTCCAGAGACAAGA[A/G]GATATTCACGGAGGC	84900
rs141333689	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116837513	TTCCTTTTTAACATC[A/G]ACAAGCATTTTTGTT	84900
rs141358702	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783515	CAGCTGCCTCGTCAA[A/G]GTGGACCAGCTCCTG	84900
rs141366599	snp	A/G	0.0126979	0.078662	intron-variant	RNFT2	GRCh38.p7	12:116840590	GGAATCAGAGTTCTT[A/G]ACACCTACCTCTGAC	84900
rs141400770	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116778235	CCCCAGCAAAACTCA[C/T]GTTGAAATTTGATCC	84900
rs141430372	snp	C/T	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116747918	ACCCTCGGCCGGGCA[C/T]GGTGGCTCATGCCTG	84900
rs141435711	snp	C/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116803777	TCTGGAGAGCCTTGA[C/G]TAGCAGGGGGATGAG	84900
rs141473931	snp	A/G	0.0310518	0.120672	intron-variant	RNFT2	GRCh38.p7	12:116809858	TTTGTATTTTTTAGT[A/G]AAGACAGGGTTTCAC	84900
rs141495044	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116820631	TTTCTCTTTCTCCCA[C/T]ATCTTACTTTATCTC	84900
rs141495653	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116773620	CTTTCCCTGAGGATG[A/G]CAGTGGTGAGCACAT	84900
rs141503581	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831321	CAGAAGTGATACTGT[A/G]TCTTTTCAGGACATC	84900
rs141518407	snp	G/T	0.0026839	0.0365342	intron-variant	RNFT2	GRCh38.p7	12:116849275	CGAGGCAGACGCTCA[G/T]TAAAGAGTCCTGGTG	84900
rs141527456	snp	G/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740061	AAATACAAAAATTGG[G/T]TGGGCGTGGTGTCGC	84900
rs141560897	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116787179	TGTCCAAAAAACACC[C/T]AGTTGCTCAGTTATA	84900
rs141562865	snp	G/T	0.0275645	0.114116	intron-variant	RNFT2	GRCh38.p7	12:116824482	TAAGCAGCCCGAGCC[G/T]GGGAGTATGACACCT	84900
rs141563907	snp	A/G	0.0240643	0.107019	intron-variant	RNFT2	GRCh38.p7	12:116758701	CCCCAATCCCTTCTA[A/G]CTTGTAGGGTTTCTG	84900
rs141614443	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116828032	CAGCAGGCAGGGGCT[C/T]CCAGAGACACAGGGA	84900
rs141634009	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737081	ACCGGGCAGGTGAAA[A/T]GCAGGGAGGTGTTCA	84900
rs141695093	snp	G/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116793640	AAGCACCCAGCGCCT[G/T]CCTTCTCAGGCTTTT	84900
rs141763120	snp	C/T	0.029116	0.117091	intron-variant	RNFT2	GRCh38.p7	12:116762854	TGACCTCAGGTGATC[C/T]GACCACCTCAGCCTC	84900
rs141787461	snp	A/G	0.0452528	0.143452	intron-variant	RNFT2	GRCh38.p7	12:116844165	GAGGCTGCATCGCCT[A/G]CGAGGAGGTCATCAC	84900
rs141825883	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116750359	TTCACAGGCAGGCTG[C/T]CTGCAGCCGGTGGGG	84900
rs141836449	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761500	CCATTCCTCTTATGC[C/T]GCTGGGTGGACATAG	84900
rs141842063	snp	A/G/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116790654	TGAGATACAATTCAC[A/G/T]TAACATAAAATTAAC	84900
rs141891522	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116758868	TGCGATGAATTTCCC[A/G]GGTGTTCTTTGTGCT	84900
rs141894142	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116839045	GAATGACTTGGTTGC[A/G]ATGTTGCTTCCTCCA	84900
rs141915909	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116805245	TTTTCTTTGCCTAAC[A/G]GAGGTAATAGCGGGC	84900
rs141918610	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835269	GAACCCAGGCAGGCT[A/G]CCTCTAAAGCCATAA	84900
rs141929976	snp	C/T	0.102014	0.201495	intron-variant	RNFT2	GRCh38.p7	12:116801982	ACCTGCCACCATGCC[C/T]AGCTAATTTTTGTAT	84900
rs141964367	snp	A/G/T	0.0349115	0.127424	intron-variant	RNFT2	GRCh38.p7	12:116769943	GGGAGGCTGAGGCAG[A/G/T]AGAATCATTTGAACC	84900
rs141974041	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116807327	TGCCATTAGGGACCC[A/G]TGATAGTAATAAAGT	84900
rs141982973	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116802388	GTAAATAAAGTTCTG[C/T]TGGAAACCAGCCATG	84900
rs141983067	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116838525	CAGTATGACACAGCC[A/G]CTTGCTTCTTCCCTC	84900
rs142052163	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116807662	CAGCCACTGCTCCCT[A/G]TGCACCTGCAGAACC	84900
rs142101133	in-del	-/A	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116786287	CCACCACGCCTGGGT[-/A]ATTTTTGTATTTTTA	84900
rs142108226	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761239	CTGTAACCTCTGCCT[C/T]CCAGGTTCAAGCAAT	84900
rs142109517	snp	G/T	0.021333	0.101051	intron-variant	RNFT2	GRCh38.p7	12:116752455	TTTTTGTTTTGTTTT[G/T]TAATCAAAGAGAAGA	84900
rs142124579	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116840318	AATAGAGACAAAGAA[C/T]CAGGCTCAGAAAAAC	84900
rs142211650	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116757287	TCAGCTTCTTGTTTC[A/G]TTTATCTTTTGAATT	84900
rs142224073	snp	A/G	0.0603597	0.1629	intron-variant	RNFT2	GRCh38.p7	12:116749378	AACCTCCTGGGCTCA[A/G]GTGATCCTCCCACCT	84900
rs142234367	snp	C/T	0.0490535	0.14873	intron-variant	RNFT2	GRCh38.p7	12:116805582	CGGGTTCCAGCAAGT[C/T]TCGTGCCTCAGCCTC	84900
rs142249804	snp	C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116775903	TAAAAATTAGCCTGG[C/T]GTGGTGGTAGGCATC	84900
rs142287298	snp	A/G	0.0696718	0.173152	intron-variant	RNFT2	GRCh38.p7	12:116768321	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	84900
rs142295303	snp	A/C	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116826551	TGCTGGGATATGCCC[A/C]GTTTTCCTTGGTGGT	84900
rs142316057	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116818678	AAGCCTTCCTCTTTT[C/T]CTGGGGAAGGTGGTG	84900
rs142337491	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116850594	GAATCCCTGTGAGCC[C/T]TGTGAAGTATTTTTT	84900
rs142349408	snp	C/G	0.239614	0.249784	intron-variant	RNFT2	GRCh38.p7	12:116786352	CTGACTTCAGGTGAT[C/G]CACCCACCTCGGCCT	84900
rs142350220	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116822905	GGGAGGCTGAGGCAC[A/G]AGAATCACTTGAACC	84900
rs142404148	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816754	CTCATGGGGTTGTTA[C/T]AGTCTATTTTTAAAG	84900
rs142455219	in-del	-/TAAAA			intron-variant	RNFT2	GRCh38.p7	12:116800812	AGCAAGACTCCATCT[-/TAAAA]TAAAATAAAATAAAA	84900
rs142515924	snp	G/T	0.046775	0.145601	intron-variant	RNFT2	GRCh38.p7	12:116766125	AAAAAATAAAAATTT[G/T]TTTTTAATTAGCCAG	84900
rs142567774	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787554	TTATAATAAAAATAA[A/C]AATAAAAATCAATTA	84900
rs142597943	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116775484	TACCACTGAGCTTGA[A/G]TCTTCTCAGGATTTG	84900
rs142608398	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116833101	TTTTTGTATTTTTAG[C/T]AGAGTTGGGGGTTCG	84900
rs142614320	snp	A/G	0.00953873	0.0683987	intron-variant	RNFT2	GRCh38.p7	12:116788133	TGTTTCTCCATGTTG[A/G]TCAGGCTGGCCTCAA	84900
rs142641164	snp	A/G	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116742519	CGATCTGTCCGACTT[A/G]GCCGCCCAAGCTCCT	84900
rs142675687	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820342	CTGCCTCGGCCTCCC[A/G]TAGTTCTGGGTTTAT	84900
rs142679592	snp	A/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739877	CCCAATCAGGACTCT[A/T]AGTTTGACAATAGGA	84900
rs142704483	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116784965	AATTTAAACCCTCCA[C/G]GGGCTGCCCTTGTGC	84900
rs142757427	snp	A/G	0.0275645	0.114116	intron-variant	RNFT2	GRCh38.p7	12:116831078	GCCCCTTCAACTTGG[A/G]GCCAGGTGCAATGGC	84900
rs142782734	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116829383	GAAACCAGCATTTCC[C/T]TCCAGGGGATGTTTC	84900
rs142823028	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784605	TCCCCAAAGCCTGGG[C/T]TTCTTCTCATTGTTC	84900
rs142841506	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116843258	AGCATTTTGGGAGGC[C/T]GAGGCGATTGGATCC	84900
rs142842447	snp	C/T	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116795711	AGTACAGGTAGCAGA[C/T]GGAGAAACATAAAAG	84900
rs142899873	snp	C/T	0.0722614	0.17581	intron-variant	RNFT2	GRCh38.p7	12:116763003	AGGAGGATTGCTTGA[C/T]CCCAGGAGTTTGAGG	84900
rs142926115	snp	A/C/T	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116744184	CGAGCAGAGATCATG[A/C/T]GACTGCACTCTAGCC	84900
rs142936204	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791384	ATCATGATCTTGGCT[C/T]ACTGCAACCTCTGCC	84900
rs142946032	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116850937	CACACCTGGCCCAAA[A/G]TATTTTCAAAATACA	84900
rs142964268	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116748969	TGATGGGAGGATTTA[A/G]TAAGTTAATCAATGC	84900
rs143025126	in-del	-/C			intron-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116825031	TTGTCTCTCCTCCCC[-/C]ATGATATCTGCTGGG	84900
rs143048316	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116797245	CCAGGACCTCAGAAT[C/T]TGGCTATATTTGGAA	84900
rs143052631	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116777543	ATGGAGAACTGTAAC[G/T]GCAGCCAGGATGTCT	84900
rs143068431	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116834942	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATTC	84900
rs143089780	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116753293	GTAGCTGTGACTACA[A/G]GCACATGCCACCATG	84900
rs143103109	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786601	CTTTCTCATAGTCCA[C/G]CTCTTCCAAGGCTCT	84900
rs143121585	snp	C/T	0.0126979	0.078662	intron-variant	RNFT2	GRCh38.p7	12:116847019	GTTCAAACGATTCTC[C/T]TGCCTTAGCCTTCCA	84900
rs143130675	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116785695	TAAGTGAAATGGCAG[A/G]GAAACTGAAGTTAGC	84900
rs143272854	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116817126	CAAGCGATTCTCATG[C/T]ATCAGCTTCCCAAAC	84900
rs143274842	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783283	GAGAATCCTAGCCAG[A/G]TGATTATTTCCATAG	84900
rs143291595	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116762507	CTCAGGAGGCTGAGG[C/T]GGGAGGATCCCTTGA	84900
rs143299865	snp	G/T	0.00874735	0.0655527	intron-variant	RNFT2	GRCh38.p7	12:116819160	CTGACTTCAAGTTTA[G/T]GGGAGCTGATGAGGT	84900
rs143307928	snp	A/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116842771	TAGGGACGGGGTTTC[A/G]CCATGTTAGCCAGGC	84900
rs143372265	snp	A/G	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116769345	ACAGAGTGAGACTCC[A/G]TCTTAAAGTTAACTG	84900
rs143405309	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116814985	AGGTGACCCGCCTGC[A/G]TCGGCCTCCCAAAGT	84900
rs143419032	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829555	GTAGATGTGGGTGTA[C/T]GTGCTCCAAGGAATC	84900
rs143421255	snp	A/C/T	0.000335256	0.012943	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737838	CGACAGCCCGAAGAC[A/C/T]AGGGCGAGCACCCAC	84900
rs143426379	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116779860	ATAGAGAAAGGCCTC[C/T]AGGCAGGTGTTGGAA	84900
rs143515479	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801684	TTAAAGTGAGTAAGA[A/C]AGTTAGAATCTAACC	84900
rs143536947	snp	A/G	0.00755907	0.0610114	intron-variant	RNFT2	GRCh38.p7	12:116741636	AAGGCCCACCTTCCA[A/G]TACGATCAAATTACA	84900
rs143550824	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116799907	ATTGTTGGAGGTGGC[A/G]CTTAGTAGGAGTTGT	84900
rs143568878	in-del	-/TAGA	0.0505692	0.150756	intron-variant	RNFT2	GRCh38.p7	12:116789439	TGGGTGGATGGATGG[-/TAGA]TGGATGGATGGATGG	84900
rs143580547	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116827650	TTACCTATTGTCCAC[A/G]GCTATTTTCCTACTG	84900
rs143631617	snp	G/T	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116744998	CAGAAAAAGCTCAAG[G/T]CCCCTTGAGGATCAT	84900
rs143688702	snp	A/C	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116823649	AAATTGCACCACTGC[A/C]CTCCAGCCTGGGTAA	84900
rs143695481	snp	A/C	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116832867	AAGGTCAGGTTCAAT[A/C]CCAGCCCAGTGTGAG	84900
rs143697394	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796814	CATAACATTCTGTGT[A/G]TAAAGACACAGTGCC	84900
rs143723292	snp	A/G	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116789389	AGAGTGAGTAGATGG[A/G]TAGATGAGTGGATGA	84900
rs143785721	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116784297	TAGGCAGCATCCGCC[A/G]CACGTGTCGTGTCCT	84900
rs143819602	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116786085	TGATTACTCTTATCA[A/G]TGGATGAGGCGATGG	84900
rs143841382	snp	G/T	0.0372196	0.131242	intron-variant	RNFT2	GRCh38.p7	12:116845222	GCACTCAAGCCTGGA[G/T]GACAGAGCAAGACCC	84900
rs143908855	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816253	CAGTTGCTGGGGCAC[A/G]TGCGCTGGGCCCTTC	84900
rs143908897	snp	C/G	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116781934	ATACAAAAAAATTAG[C/G]TGGGCGTGGCAGCAT	84900
rs143911352	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826188	CTTCATTTCCCACCC[A/G]CTTCTGGAGCCAGCC	84900
rs143960161	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116791259	TGGCTTCTCTCATGC[C/T]GTGCTATGTTTTCGA	84900
rs143967639	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116813649	GATCAAGTCTCTTGT[A/G]TATTTCATTTTATTC	84900
rs144006862	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116759892	GTGGTAGCGTGGCGA[A/G]GAACCCGTGGAGCTC	84900
rs144027936	snp	C/G			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836489	ACCTCTCTGAGGCTT[C/G]GTTTCCTTAGTAAGA	84900
rs144034106	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116756909	AAAAGATTGGTACCA[A/G]TTCTTCGAATGTCTG	84900
rs144043107	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116848311	GCAGTGAACGTATGC[A/G]TGCATGTATCTGTTT	84900
rs144160406	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787038	CCTCCCCATGCCGAT[A/G]TCCTTAATCACATCT	84900
rs144185984	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770519	TGATGAATGTAACAG[C/G]TTTTAAAAGTTATTT	84900
rs144211077	snp	C/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779302	CCATCGCCCTCAAGT[C/G]CCTCATCGTGGCCCT	84900
rs144219791	snp	A/G	0.00795532	0.062565	intron-variant	RNFT2	GRCh38.p7	12:116774512	CTGTTTGTGGAAACT[A/G]TCAGAGCTGTCAGAA	84900
rs144230013	snp	A/G	0.0360663	0.129354	intron-variant	RNFT2	GRCh38.p7	12:116753182	TTGAGACAGAGTCTT[A/G]CTCTGTTGCCCAGGC	84900
rs144233958	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116809368	TTCGTTGTGAGGTTT[C/T]GGCAACTCCTTCATG	84900
rs144302629	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116802910	ACCCAGCCTGGGTGG[C/G]ATGGTGAAACTCTGT	84900
rs144342080	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831196	ATGACCTCGTCTCTC[C/T]ACAAAAAAAAAAAAG	84900
rs144362851	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747512	AGCCTGGGCAACAGA[A/G]TGAGACCCCCGTCTC	84900
rs144402236	in-del	-/ATTATTCCAAGTGCCTTCTTTTTTAT	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116846249	TACTATTTGCCAGTC[-/ATTATTCCAAGTGCCTTCTTTTTTAT]ATTATTGTTATTTTT	84900
rs144446658	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116814383	CATTGTTTGCAGGGC[A/G]GGGAAGGGAGGGCGA	84900
rs144457693	snp	G/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116750926	TTTTTTTGAGACAGG[G/T]TCTTGCTCTTTCAGC	84900
rs144482364	snp	G/T	0.00557542	0.0525036	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853790	ATTTATTACAGCAGT[G/T]CTCCCACGAGAAACC	84900
rs144486924	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116740914	ATACTTTGGAAAATG[A/C]CAGAGAGCACTAGGG	84900
rs144505609	snp	A/G	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116764279	AGGTGATGGGTGCAC[A/G]AAAATCTCACAAATC	84900
rs144513613	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116820856	CAGAGTCTGGGGACA[G/T]CCTGCAGGTACTAAG	84900
rs144527104	snp	A/C	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116779625	GCAATTTTCATCCAC[A/C]TTTCACCTGAGAGAG	84900
rs144535408	snp	A/G	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116784752	TCATTTTGCCTCCCC[A/G]GTGACGTGGGAGCCC	84900
rs144540144	snp	A/G	0.0640965	0.167152	intron-variant	RNFT2	GRCh38.p7	12:116836763	AACCCTGTCTCTACT[A/G]AAAAAAAAATACAAA	84900
rs144623565	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116816672	TAAGCTTAGGCAAAA[C/T]GGTGAACTTCTCTGA	84900
rs144676241	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116838844	CAGACAAGACACCCA[C/T]TGTCCCAGATCTAGG	84900
rs144757010	snp	G/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116827301	ACAGGAGCACCTGAT[G/T]CAATTAAAAAGTCAG	84900
rs144791182	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761305	AGACACACACCACCA[C/G/T]GCCTAGCTAATTTTG	84900
rs144802907	snp	C/T	0.0174175	0.0916809	intron-variant	RNFT2	GRCh38.p7	12:116743986	AATCCCAGCACTTTG[C/T]GGGGGTAAGGCAGGC	84900
rs144804369	snp	A/G	0.00517822	0.0506191	downstream-variant-500B	RNFT2	GRCh38.p7	12:116854010	GACTCTCCCCTAAGA[A/G]GCTCCAAGGGGAAGC	84900
rs144816926	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116770347	AGAGTAATAGGCTAT[A/C]TCATATAGCCTAGAT	84900
rs144822718	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116792658	GAATAGTCTTCCCCA[A/G]GATAAATTGCAGGCT	84900
rs144825117	snp	A/G	0.0189856	0.0955633	intron-variant	RNFT2	GRCh38.p7	12:116828932	GCAGGAGGATCACTT[A/G]AGCCCAAGAGATGGA	84900
rs144854262	snp	C/T	0.0722614	0.17581	intron-variant	RNFT2	GRCh38.p7	12:116764644	CGCCTATAATCCCAG[C/T]ACTTTGGGAGGCTGA	84900
rs144898957	snp	C/G	0.0225045	0.103662	intron-variant	RNFT2	GRCh38.p7	12:116839447	GATGGATGGATGGAT[C/G]GATGGATGGATGGAT	84900
rs144901530	snp	G/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116824439	TAAATTTAAAAAATG[G/T]ATCTCTTTCTCATGT	84900
rs144930883	snp	A/G	0.0240643	0.107019	intron-variant	RNFT2	GRCh38.p7	12:116792015	GAATTATTAGACCGC[A/G]GTCCTTCCCGTGTAT	84900
rs145009051	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837251	CCAGGAAGGAGAGGC[A/T]GAGGGCCCACAGATC	84900
rs145056283	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116830132	CGAGTTCCCATATAC[A/C]CTTCATTCCTCTTCC	84900
rs145060332	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116751421	CTGTTTGTTTGTTTT[A/G]ACATGGAGTTTTGCT	84900
rs145066579	in-del	-/AG	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116845459	GCAACATCATAAAAC[-/AG]GGGAGACATGATTGC	84900
rs145100722	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116783692	AGAAGTGGCAATGTC[C/T]TCCACCTTTCCTTAG	84900
rs145123916	snp	C/T	0.0298908	0.118541	intron-variant	RNFT2	GRCh38.p7	12:116752051	TTGTGGTCTACTACT[C/T]TCCATGAGAAAATAT	84900
rs145169344	snp	C/T	0.00914312	0.0669923	intron-variant	RNFT2	GRCh38.p7	12:116837572	GAAGGGGGAGGTTGT[C/T]TTTCATGTTCAATTG	84900
rs145174477	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781346	TTGGGTTCAGCTGAT[G/T]GGAAGCCCAAGAGGA	84900
rs145187695	snp	C/T	0.0287284	0.116357	intron-variant	RNFT2	GRCh38.p7	12:116761922	AATAGTGCATCCAGG[C/T]CGGTCGCGGTGGCTC	84900
rs145198263	snp	G/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116810205	ACTCCAAGGCCCTCT[G/T]GGAAAACAGAGAATG	84900
rs145260035	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116778588	GACAGCAGTGGCTTA[C/T]GCCTGTATCCCAGCA	84900
rs145271225	snp	C/T	0.0162398	0.0886349	intron-variant	RNFT2	GRCh38.p7	12:116792308	GCCCACCTCGGCCTC[C/T]CAAAGTGCTGGGATT	84900
rs145299038	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807034	TAGATCTCATTGGCC[A/T]CCACTCAGTCACACT	84900
rs145310761	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832925	TTTTTTTTTTTTTGA[A/G]ATGGAGTCTTGCTCT	84900
rs145322638	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803196	TTCACAACAGCAGAG[A/G]AAACACCTGGTCTTG	84900
rs145329004	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116758041	TTAGAATTGTGATAT[C/T]TTCCTGTTGGACAAG	84900
rs145415821	snp	A/G	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116767930	TATCTTACATATACA[A/G]CTCATGTCAGTTCCA	84900
rs145433436	snp	G/T	0.0463947	0.145069	intron-variant	RNFT2	GRCh38.p7	12:116762934	GTTTTTTTAAAAAGT[G/T]AGCCAGGTGTGGGGG	84900
rs145433631	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116848761	TAAAGTTGTCCTTAA[C/T]GTCCCAACCCGCCCA	84900
rs145453946	snp	C/T	0.0551013	0.156571	intron-variant	RNFT2	GRCh38.p7	12:116810985	TGGATTGGAAAGAGC[C/T]TGGGCTCTGGAGTCA	84900
rs145502729	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116765785	CTTTGAGAATTAGGT[A/G]TATAAGCTTGGATTT	84900
rs145509848	snp	A/G	0.000173762	0.00931938	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836229	ACAGAAGCTGGTGAC[A/G]TCTGCGCCATCTGTC	84900
rs145516316	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116826362	GCACGTCCTGCAACA[A/G]TTGCTACCGTTTCCC	84900
rs145584897	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116793800	AGTGCTTTTCTCCAA[C/G]CTGCAGTATTCCACC	84900
rs145599226	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853084	CTGAGGTTTTCTTCT[C/T]GGTGGGGGGATTTAA	84900
rs145665160	snp	A/G	0.0275645	0.114116	intron-variant	RNFT2	GRCh38.p7	12:116822731	AACTGGCTGGGTGCA[A/G]TGGCTCACACCTGTA	84900
rs145673228	snp	G/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116764800	GGGAGGCTGAGGCAG[G/T]AGAACCACTTGAACC	84900
rs145737339	snp	A/G	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116774984	GAGGAGCAACAGGCC[A/G]TGTGCGGTGGCTCAC	84900
rs145743159	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116830665	ATTTTAGCACTTTGG[A/G]AGGCTGAAGTGAAGT	84900
rs145776596	snp	A/G	0.0352966	0.128072			GRCh38.p7	12:116777127	TTCACCATGTTGGCC[A/G]GGCCGGTCTCAAACT	84900
rs145779043	snp	C/T	0.000399281	0.0141238			GRCh38.p7	12:116765226	TTTGGTTTGGATTCA[C/T]AGAGAATTAAACTGG	84900
rs145786463	snp	C/T	0.00795532	0.062565			GRCh38.p7	12:116823237	AGAGGCCCAGAATGG[C/T]GGAGCTGGGTCAACA	84900
rs145798126	snp	C/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739616	GCCACATTTAGAGGA[C/G]AAAGTATTCCAAGGG	84900
rs145808051	snp	A/G	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116786032	ACTCCAGCCTCGGCA[A/G]TAGAGCCAGCCTCTC	84900
rs145840731	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780439	AGGAGAATCTACTGC[C/T]GCAGCTGATCTGATG	84900
rs145868621	snp	A/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738871	TTCCCCCAAGGATTT[A/G]CAATGTGGGATAATG	84900
rs145879851	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116818157	CCCCCTCTCTACAAA[A/G]AAAGTCTTTAAAAAA	84900
rs145882549	in-del	-/G	0.26518	0.249539	intron-variant	RNFT2	GRCh38.p7	12:116790373	ACCCCTGTATTCGTG[-/G]AGTTTATATCCTCTT	84900
rs145906065	snp	A/G	0.0271762	0.113356	intron-variant	RNFT2	GRCh38.p7	12:116808050	CTCACTACAACCTCC[A/G]CCTCCCAGGTTCAAG	84900
rs145932622	snp	A/T	0.0368353	0.130617	intron-variant	RNFT2	GRCh38.p7	12:116759921	TCTAGAACTCTCGAG[A/T]TTCTATGGCCTTTGT	84900
rs145937056	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853401	AGGGAATAAGAAAGG[A/C]AAGCTTTGGACACAG	84900
rs145937515	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116816894	AGTTTCTTAGAAACC[C/T]CTTGTGTATATCTCC	84900
rs145950975	snp	A/G	0.0505692	0.150756	intron-variant	RNFT2	GRCh38.p7	12:116763783	GACTCCATCTCAAAA[A/G]AAAAAGGGGGCGGGG	84900
rs146016192	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116820446	ATTTCAAGTGCTCCA[C/T]AGCGACATGTGACCA	84900
rs146056537	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116832475	TCTTCCATTGATGGG[C/T]GTCTGGGCTGCTTCC	84900
rs146059966	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774613	CTCAAGTCAGCCTTT[C/G]AGATCACATCCATCT	84900
rs146138343	snp	C/T	0.00914312	0.0669923	intron-variant	RNFT2	GRCh38.p7	12:116835041	TTTTAGTAGAGATGG[C/T]GTTTTACCATGTTGG	84900
rs146141733	snp	C/G	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116777647	CTCATCTGCAAAATG[C/G]GGTGGATAAAAGTAC	84900
rs146142069	snp	C/T	0.00226816	0.0335996	intron-variant	RNFT2	GRCh38.p7	12:116741103	CTGAAAGGTAGGCAT[C/T]CCTGCTTCTGTTCCA	84900
rs146143668	in-del	-/AATAA			intron-variant	RNFT2	GRCh38.p7	12:116800831	ATAAAATAAAATAAA[-/AATAA]ATAAAATAAAATAAA	84900
rs146153464	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744544	CCAGGAAGTAGCAGG[G/T]CTGAGATTTGGGCCC	84900
rs146181982	snp	A/C	0.00874735	0.0655527	intron-variant	RNFT2	GRCh38.p7	12:116787418	ATACTGTAAAGGTAA[A/C]AAGACTTGACAGGGC	84900
rs146197790	snp	C/T	0.0193772	0.0965046	intron-variant	RNFT2	GRCh38.p7	12:116743039	TGAGCTATGATTGCA[C/T]CACTGCATTCCAGCC	84900
rs146258617	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116850524	GACTTGATGGTGCAG[A/G]CTGGGGAGGAGCCTA	84900
rs146260285	snp	C/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116790748	GATCTCTTGAGCCCA[C/G]GAGTTCAATACCAGC	84900
rs146270391	snp	C/G/T	0.00034196	0.0130718	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766871	CTGGCGGGGAACACC[C/G/T]TCTATGTGCTTTATA	84900
rs146279571	snp	C/G	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116759153	TTCAATTCTATTGCC[C/G]AGACTTTCCAGAGCA	84900
rs146300219	snp	C/G	0.0138799	0.0821421	intron-variant	RNFT2	GRCh38.p7	12:116802603	CAAACAATGCCACCA[C/G]CCACCAGGAACTGGG	84900
rs146332976	snp	G/T	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116786388	AGTGCTGGGATTACA[G/T]GCATGAGCCACCGCG	84900
rs146381180	snp	A/C	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116805840	TCTTGTTCTTACAGC[A/C]CTTCAGCTGATTGGA	84900
rs146399067	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116774346	AAAGATCATCTACCA[C/T]TGACATCATTTCATA	84900
rs146437921	in-del	-/TAAATGGGAGGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116788849	GGATGGATGGATGGA[-/TAAATGGGAGGAGAG]TGGATGGATGAATGG	84900
rs146444096	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848493	GCCAAAGACCTCACA[A/G]TGGCCCACAAGTACC	84900
rs146445043	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116811565	ATTTTTAGTAGAGAC[A/G]AGTTTTCGCCATGTT	84900
rs146445594	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116754631	TGTTCCCTGTCCACC[A/G]CATTCACACTAGCAT	84900
rs146463217	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814048	GTAAGCAGAGGAAAC[A/G]GGGCCTTGGAAAACA	84900
rs146468491	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816295	GCCGATGCTCTTAGA[C/T]CAAGGGAACCATGGC	84900
rs146539797	snp	A/C	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739186	TATCCACAATATTGG[A/C]TCTGCCTCCAGAGAC	84900
rs146567981	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116826890	GGGAGGGATGGATAG[C/T]AAAAATAATTTTTTA	84900
rs146572050	in-del	-/CGTTGGCCAGGCTGGC	0.0836354	0.186609	intron-variant	RNFT2	GRCh38.p7	12:116850834	GATGGGGTTTCACCA[-/CGTTGGCCAGGCTGGC]CTCAAACTCCTGACC	84900
rs146586612	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116829478	ACAACTGGAGGTGGC[A/G]AACTAGTCACAAAAA	84900
rs146679018	in-del	-/T	0.0441095	0.141807	intron-variant	RNFT2	GRCh38.p7	12:116823902	CTACCATTAGCCCCA[-/T]TTTACTAGCGAGGAA	84900
rs146687132	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783453	GAGAGCTATACTGTC[A/G]GCTTCCTGGGGACCA	84900
rs146703103	snp	C/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116844881	CATTTGGTTGGTCAA[C/T]AGATATTTACTGAGC	84900
rs146705795	snp	A/G	0.0134861	0.0810011	intron-variant	RNFT2	GRCh38.p7	12:116785751	TTATTTTCAGCAGAC[A/G]AAAATAAAACAGGAA	84900
rs146727689	snp	A/T	0.00914312	0.0669923	intron-variant	RNFT2	GRCh38.p7	12:116829608	AGCCCATCAAGATGG[A/T]ATATAAAAGTTGGCT	84900
rs146807201	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833076	CAGGTGCGCCACCAC[A/G]CTCAGCTAATTTTTG	84900
rs146807397	snp	G/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739255	GTAGATGGCCCTTAT[G/T]ACCTTGCTAGGGTGA	84900
rs146807588	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796845	CCATCCTGGAATAAG[A/G]ACTTCGAGAAGAGCC	84900
rs146819064	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742014	TCTGAGAAACAACAC[A/G]GAGAGGCTAATGACA	84900
rs146826466	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116800090	CCCCCTTCACCTTCT[A/G]CCATGAGTAAAAGCT	84900
rs146850072	snp	A/C	0.0310518	0.120672	intron-variant	RNFT2	GRCh38.p7	12:116845801	TCTCCTTTCCCCAAT[A/C]CCTCTCTCCCCTGCA	84900
rs146893965	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848793	GCCCTCCCTGTTCCT[C/T]CTCCCTCCTGCTTTT	84900
rs146920941	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116743424	GGCACGCACCACCAC[A/G]TTTGGCTAATTTTTT	84900
rs146925954	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801189	TGCTGAGCCCAGGGG[A/G]TGCCCTGTCTGCCTG	84900
rs146941648	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116803827	CCTCAACATCAGGGG[A/G]CCAATGAGGGAAGGG	84900
rs146943922	snp	C/G	0.0755793	0.179102	intron-variant	RNFT2	GRCh38.p7	12:116747983	ATCACATGAGGTCAG[C/G]AGTTCAATACCAGCC	84900
rs146945188	snp	C/G	0.0228947	0.104514	intron-variant	RNFT2	GRCh38.p7	12:116831095	CCAGGTGCAATGGCT[C/G]ATGCCTATAATCCCA	84900
rs147030244	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116815686	TTCATCACATCTGCA[C/T]GTGCACAAAATTCCT	84900
rs147046728	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116818363	GTCTGCAAACCTGGG[C/T]TGGTAATATCCCTCC	84900
rs147048841	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761618	CAGCAGGTTCATCCC[A/G]GCAACCTGGGAGGGA	84900
rs147050646	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116847154	CCTCAGTGATCCCCC[C/T]GCCTCAGCCTACCAA	84900
rs147065882	snp	C/T	0.00095183	0.0217947	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849467	CGAACACTGAGGACA[C/T]CCAGAAGGACGCCAA	84900
rs147170523	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828066	TTCATGGGGTAGCCG[C/T]GTCCTTACCTGTCAT	84900
rs147172449	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769479	ATGTGGAGGTGGAAG[A/T]CAGTGATATTGATGA	84900
rs147191776	snp	C/T	0.0279526	0.114869	intron-variant	RNFT2	GRCh38.p7	12:116812825	CAGCCCTAGCCAGGC[C/T]CAGTGGCTCACACCT	84900
rs147227760	snp	A/G	0.0217236	0.101931	intron-variant	RNFT2	GRCh38.p7	12:116810555	TCACAGGGCAAAGCA[A/G]GGAGACTCACGTTCT	84900
rs147260843	snp	G/T	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116781935	TACAAAAAAATTAGC[G/T]GGGCGTGGCAGCATG	84900
rs147277737	snp	C/T	0.029116	0.117091	intron-variant	RNFT2	GRCh38.p7	12:116784323	GTCCTCTTACAATTC[C/T]CCAGTTCAGCTCTTG	84900
rs147297000	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116828380	GCTGGTTCATGGCTC[A/G]CACTTTGGGTGGCTG	84900
rs147331031	in-del	-/A	0.0356815	0.128715	intron-variant	RNFT2	GRCh38.p7	12:116795115	CATTGCCTCTTTATG[-/A]AAAATGAAGGCCGGG	84900
rs147334791	snp	C/T	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116826397	ACGGTGGCAGGGAGG[C/T]GAGACAGCTCATAAT	84900
rs147383426	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797484	GACTCACTTGAACCC[A/G]GGAGGTGGAGGTTGC	84900
rs147384549	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739974	ACTTTGGGAGGCCAA[C/G]GCAGGCGGATCACTT	84900
rs147403142	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116843586	CCCATCAATCCACCC[A/G/T]ATCCTATCCTTCCCA	84900
rs147414728	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116753305	ACAGGCACATGCCAC[C/T]ATGTGTGGCTAATTT	84900
rs147483590	snp	C/T	0.0287284	0.116357	intron-variant	RNFT2	GRCh38.p7	12:116756713	ATCTTTTTGGTAATT[C/T]GTTGGATTCGGTTAG	84900
rs147487831	snp	A/G	0.0471551	0.14613	intron-variant	RNFT2	GRCh38.p7	12:116812596	CTGGAGTTCAGTGGC[A/G]CGATCTCAGCTCACT	84900
rs147565112	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116805192	CATCACTTCCTCTAT[C/T]GCCCACTGCTTGGTG	84900
rs147614092	snp	C/T	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116778798	GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG	84900
rs147634302	snp	A/G	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116807229	GAAGCTCAGCAAGGT[A/G]TGTTCACTTATCCAG	84900
rs147669904	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116818643	GAAGGGAGGGTGTAT[A/C]GTCCACTGTCAACAT	84900
rs147718121	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791486	CTGGCTAATGTTTGT[A/G]TTTTAGAGAGATGGG	84900
rs147720166	snp	A/G	0.000148269	0.00860886	utr-variant-3-prime, synonymous-codon	RNFT2	GRCh38.p7	12:116852685	GAAATTGGAGCTGGA[A/G]AAGATTGATGAAAGT	84900
rs147755621	snp	G/T	9.03644e-05	0.00672116	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737800	CTGACCTGCTTGAAG[G/T]TGCTGCTGAGGAAGT	84900
rs147768631	snp	G/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116776184	ATAGAAAAACACTTT[G/T]GCACCCACCCCCCAA	84900
rs147772582	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116833660	TAGGAGCTGGCCTGA[A/G]TGCTTTCCAGAGCTG	84900
rs147824017	snp	G/T	0.031825	0.122064	intron-variant	RNFT2	GRCh38.p7	12:116751131	ATATTGCCCAGGCTG[G/T]TCTCAAATTCCTGGG	84900
rs147837374	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779711	CCTAATAGGTTTTGA[C/T]TCTTCGTGGCTTCCA	84900
rs147841479	snp	A/T	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116836841	AAGCTGAGGCAGGAG[A/T]ATTGCTTGAACGCGG	84900
rs147853224	snp	A/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116747517	GGGCAACAGAGTGAG[A/G]CCCCCGTCTCACTCT	84900
rs147877999	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116849254	CCCTTCTCCTGCTCC[C/T]GAGACCGAGGCAGAC	84900
rs147879685	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788733	TATGTATACATGTGT[A/G]TTTGAGTGGGTAGAT	84900
rs147929757	snp	A/G	0.0256215	0.110247	intron-variant	RNFT2	GRCh38.p7	12:116764753	AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCGCCT	84900
rs147947093	snp	A/G/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116851603	AAATTAGCCGGGCGC[A/G/T]GTGGCGGGTGCCTGT	84900
rs147950156	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116792179	CTCAGCCTCCTGAGT[A/G]GCTGGGATTACAGCT	84900
rs147966690	snp	G/T	0.0337553	0.125452	intron-variant	RNFT2	GRCh38.p7	12:116761401	AATCCGCACACCTTG[G/T]CCTCCAAAAGTGCTG	84900
rs147976487	snp	C/T	0.0134861	0.0810011	intron-variant	RNFT2	GRCh38.p7	12:116748171	CTCCAGCCTGGGTGA[C/T]AGAGCAAGGCTCTGT	84900
rs147981527	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116827698	AGTGGTGCCACAGAC[C/T]GTATGGCCTGCAAAG	84900
rs147986988	snp	C/T	9.74453e-05	0.00697948	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750183	CTCGGAGGAGGGAGG[C/T]GACGAGCAGCCTGGG	84900
rs148047696	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736365	TGAGGAGGTGTCTGA[A/G]GTGGCAGAAAACACA	84900
rs148051283	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794139	GCATAGTGTCATGCA[C/T]CTGCAGTCCCAGCTA	84900
rs148124101	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116838990	TAGGTAAATGGGTCA[C/T]GCTGATTCCTAAAAG	84900
rs148141270	snp	C/T	0.0490535	0.14873	intron-variant	RNFT2	GRCh38.p7	12:116801907	GCTCATTGCCACCTC[C/T]GCCTCCCAGGTTCAA	84900
rs148143704	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116744182	AACGAGCAGAGATCA[C/T]GCGACTGCACTCTAG	84900
rs148178384	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834797	CTCACCATATGATAT[G/T]CTTTCCAATAGTCAT	84900
rs148195032	snp	C/T	0.0217236	0.101931	intron-variant	RNFT2	GRCh38.p7	12:116797357	TTGAGGTCAGAAGTT[C/T]AAGACCAGCCTAGCC	84900
rs148247078	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852462	CATCTTTCAAGCTCC[A/G]TTACTATGGCGATGG	84900
rs148264671	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116766646	CTTCTCCGTGACCAC[C/T]GCTTGGGTATCAGTG	84900
rs148315542	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116819345	TCGGGGGCCTGGTAC[C/T]GGCGCGGGACGCCCG	84900
rs148317681	snp	A/G	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116762804	TTTAGTAGAGATGGG[A/G]TTTCACCACGTTGGC	84900
rs148322297	in-del	-/TGGA			intron-variant	RNFT2	GRCh38.p7	12:116789636	TGGATGGGAGGAGAG[-/TGGA]TGGATGGATGGATGG	84900
rs148340092	snp	A/G	0.00381166	0.0434891	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750054	CAGGGAGGAAGGAGG[A/G]GGCCGGGGCGAGGGG	84900
rs148346574	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116819109	CTTCACTCAGTGGCT[-/G]GTGAAATCCTGCAGG	84900
rs148352755	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773496	TGGCATGACTTAGCC[A/G]TTCACTGGCAGTCTC	84900
rs148356725	snp	A/G	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116831189	ACACAGCATGACCTC[A/G]TCTCTCTACAAAAAA	84900
rs148384096	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783744	TTGTTGGCTCTCCAC[A/G]GCCAGCCAGGTCAGA	84900
rs148422989	snp	C/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116821073	CGTTCCTGGCCCCTG[C/G]TAAGCGCTTAATACG	84900
rs148425739	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116764518	AGCACATTGAGGTTC[A/G]GAGTTGGGGACAGAG	84900
rs148459517	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833092	CTCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGTT	84900
rs148461513	snp	C/T	0.0115144	0.0749975	intron-variant	RNFT2	GRCh38.p7	12:116774999	ATGTGCGGTGGCTCA[C/T]GCCTGTAATCCAAGC	84900
rs148476484	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116816728	GCAAAGTGGAGGTGA[A/C]AATTTCCCCCCTCAT	84900
rs148493180	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116784962	CCCAATTTAAACCCT[C/T]CAGGGGCTGCCCTTG	84900
rs148512260	snp	A/G	2.61928e-05	0.0036188	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750205	CAGCCTGGGACGCCC[A/G]CCCCCGCCCTGTCCG	84900
rs148512932	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829107	GAGACCATGGGTGAG[A/G]GCAATTTGGGAGACA	84900
rs148543249	in-del	-/GATG			intron-variant	RNFT2	GRCh38.p7	12:116839460	ATGGATGGATGGATG[-/GATG]AATGGAAGTGAATGA	84900
rs148546064	snp	C/T	0.0142736	0.0832652	intron-variant	RNFT2	GRCh38.p7	12:116781642	GCATCTCCTGATTCT[C/T]GCCCTCCTGCCTTCC	84900
rs148580320	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795561	CTCAGTTGCACCAAC[C/G]ACGTTTCAAGGGCTC	84900
rs148633252	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791272	GCCGTGCTATGTTTT[C/T]GAGGTTCATCCATGT	84900
rs148649877	snp	C/T	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116760449	CCTTGCTCCTACCCA[C/T]TGGATCCCCGTGGTG	84900
rs148652455	snp	C/T	0.00597247	0.0543191	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836606	CACTCTCTCTCTGAG[C/T]CTTGGTTTTTCTCAT	84900
rs148668942	snp	A/G	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116803229	ATGCCAGCAGTGGAG[A/G]TTATAAAGTCCTCTG	84900
rs148684270	snp	G/T	0.00953873	0.0683987	intron-variant	RNFT2	GRCh38.p7	12:116847713	TGTATTTTTAGTAGA[G/T]ATGGGGTTTCTCCAT	84900
rs148697836	snp	A/G	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116757091	TTATCCATCTCTTCT[A/G]GGTTTTCTAGTTTTT	84900
rs148718399	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116777701	CATCACTGCTGCACC[A/G/T]CAGGGTCTGTAATCT	84900
rs148722646	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799845	AGTGTGGTGATACAG[C/T]TTGGATGTTTGTCCC	84900
rs148725557	snp	A/G	9.885e-05	0.0070296	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779310	CTCAAGTGCCTCATC[A/G]TGGCCCTGCCCAAGA	84900
rs148775272	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853992	GGGACTTCCTGCACT[G/T]CAGACTCTCCCCTAA	84900
rs148812532	snp	A/G	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116811435	GGCTGGAGTGCAGTG[A/G]GGCCATCTCGGCTCA	84900
rs148829243	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116779837	GCAATGATGCTTTGC[A/G]GTGTATCATAGAGAA	84900
rs148899973	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116827577	CTACAGGCCAAATAC[A/G]TCCTGCCACTTGTTT	84900
rs148944093	in-del	-/A	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116815335	CAAACCTTGTGGCTT[-/A]AAACAACACAACTGT	84900
rs148952544	snp	C/T	0.0566069	0.158427	intron-variant	RNFT2	GRCh38.p7	12:116742429	CATGCACCACCATGC[C/T]CGGCTAATTTTTGTA	84900
rs148975226	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116754913	ATGTACAGATTGTGA[A/C]GATTTTCTCCCACTC	84900
rs149020176	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116839812	GGAGGGGCCCACTAG[A/G]CTAAAGCCACACCTT	84900
rs149041932	snp	G/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116830273	ATTGACATTATTTTG[G/T]TTTTCAATTTTTATT	84900
rs149043452	in-del	-/TT			intron-variant	RNFT2	GRCh38.p7	12:116821833	TTTTTTTTTTTTTTT[-/TT]GAGGCAGAGTCTTAC	84900
rs149110288	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116797224	ATGTGTGTTGGAGTC[C/T]AAACCCCAGGACCTC	84900
rs149162248	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116852331	CCTTCCCCCTGCCCC[A/G]CCGTAGATTCAGGAC	84900
rs149164442	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116792480	TAGGGCCGAGGAGGC[A/G]GGGATGGACCCAGCA	84900
rs149216574	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848762	AAAGTTGTCCTTAAC[A/G]TCCCAACCCGCCCAA	84900
rs149231826	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764204	TGGGGACTCTGGGGG[A/C]AAGAGTGGGAAGGGA	84900
rs149270249	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773198	AACTCCTGACCTCAG[A/G]TGATCTGCCCGCCTT	84900
rs149272600	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853782	TGCATGTGATTTATT[A/G]CAGCAGTGCTCCCAC	84900
rs149285369	snp	A/G	0.0923359	0.194016	intron-variant	RNFT2	GRCh38.p7	12:116759096	GGATTGGGTTAATTC[A/G]AAGACCTTGTCTTCG	84900
rs149289691	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816485	CCAGAAGAGCAGAGA[A/G]AGGATCTTTATAGGA	84900
rs149343238	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116812321	CCCGACATAAATACA[C/T]GTTGAGTGACAACGC	84900
rs149359804	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116781567	CCGAGTCAGTGATGG[C/T]AGGTTGAGCGTTCTC	84900
rs149387562	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116775328	TCCTTACTGAAGTCA[A/C]CAGAAGTCACCAGTC	84900
rs149412279	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116834441	ACTATTTTAAAGTGT[A/G]TAATTAAATGGCATT	84900
rs149431950	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116828605	CCAGAACCTGGCATT[C/G]TGTCTGGTGCATAGT	84900
rs149450099	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116791134	GTCACATTCCATTCC[C/T]GCTTCCCACAAGCTC	84900
rs149483911	snp	C/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116743885	ATACATGACTTCACC[C/T]CTAGGTCTCAGCTTC	84900
rs149485709	snp	C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116826132	CTTCCAAAAAATTCT[C/T]CTCTCTGTTCATTTC	84900
rs149500747	snp	A/C	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116847325	TTGCCACCCCTGGGA[A/C]CAATCAAGACTCATG	84900
rs149503340	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116786984	CTTATAAGGACACAT[A/G]TAACGGTATTTTGGG	84900
rs149535585	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739587	ACGACATTTGCCCTG[C/T]GGGACCAAGCCCTGC	84900
rs149537985	snp	C/G/T	0.000214142	0.0103456	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779294	GTACATCACCATCGC[C/G/T]CTCAAGTGCCTCATC	84900
rs149553939	snp	A/C	0.021333	0.101051	intron-variant	RNFT2	GRCh38.p7	12:116842698	CCTGCCTCAGCCTCC[A/C]GAATAGCTTGGATTA	84900
rs149565474	snp	A/T	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116753104	AACATTAAACTTGAA[A/T]TCCTTATGGCGTTGT	84900
rs149570588	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116809051	CACAGGGCCGGAGCC[A/G]TGGCTTTTTTGGTGC	84900
rs149575210	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116831819	ATCCCCCATCCCAAT[C/T]AAGATATAAAATATT	84900
rs149600088	snp	C/T	0.0391387	0.134304	intron-variant	RNFT2	GRCh38.p7	12:116847604	ACGATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC	84900
rs149623447	snp	G/T	0.0205511	0.0992634	intron-variant	RNFT2	GRCh38.p7	12:116805489	GTTGTTGTTGTTGTT[G/T]TTTGACACAGCGTCT	84900
rs149661836	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116844871	AGTTAAGTCCCATTT[C/G]GTTGGTCAATAGATA	84900
rs149678735	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810976	GTTCCAGAGTGGATT[C/G]GAAAGAGCTTGGGCT	84900
rs149837806	snp	A/C	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116785972	TGGGAAGATTGCTTG[A/C]GCCCAGGAGGCAGAG	84900
rs149960706	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116751260	TATTTAACATAGAGC[C/G]TGAATTGAAATATTC	84900
rs150015443	snp	A/C	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116826825	TGCTAGATGCTGGGA[A/C]TATACCCAGAGTCAA	84900
rs150030174	snp	A/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116848752	GTATCTCCGTAAAGT[A/T]GTCCTTAACGTCCCA	84900
rs150048414	snp	A/G	0.029116	0.117091	intron-variant	RNFT2	GRCh38.p7	12:116757995	CATTGTTTTATAAAT[A/G]TGGGAGCTCCAGTGT	84900
rs150064372	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799423	CCCTTTTATCGTGTA[A/G]CCTGTAATATGATCT	84900
rs150103132	snp	G/T	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116837369	GCCGTGTAAGAGAGA[G/T]TCATGCAGTGTCTCG	84900
rs150119308	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116748895	AGTTACTTTCTCTCT[C/T]TGAGCCTCCATTTCT	84900
rs150134771	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790082	AGCTCAAACCTCTTA[C/T]ATTTGGTAGGTGTCA	84900
rs150139492	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116850046	GACAGGGTTTTGCCA[C/T]GTTGGCCAGGCTGGT	84900
rs150184170	snp	A/G	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116765017	TCTGTATCCATGGAC[A/G]GGCCTCCAGGGGTCC	84900
rs150201099	snp	C/T	0.0150606	0.0854603	intron-variant	RNFT2	GRCh38.p7	12:116755946	TTTTTGTACCAGTAC[C/T]ATGCTGTTTTGGTGA	84900
rs150260558	snp	G/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116812053	TCCAGGAGGAGCCCG[G/T]TGAGGAACAAATGAG	84900
rs150338944	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739356	TAAATACTTGTTGAG[C/T]GCCACTCTGTGCCAA	84900
rs150349660	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116819545	ATCTCATCCGGGCCC[G/T]GGGGAGGAGGAGGCA	84900
rs150377390	snp	A/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116772082	TATTTGTCAAATAAA[A/T]GAGTATCTCAGATTT	84900
rs150381368	snp	A/G	0.0279526	0.114869	intron-variant	RNFT2	GRCh38.p7	12:116829849	GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA	84900
rs150413379	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116784173	CCAGTTACTGCACGG[C/G]GCATTGTACAGATTC	84900
rs150414188	in-del	-/AACTA			intron-variant	RNFT2	GRCh38.p7	12:116845822	CTCCCCTGCACCCCC[-/AACTA]CAGCCACATCAGCTA	84900
rs150471733	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116842112	CTGCATCCAAGCTCC[A/G]CCGTGTGGTTGCTGG	84900
rs150488983	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752604	TAAGTGCGACCAGGT[A/G]CGGTGGCTCACGCCT	84900
rs150503049	snp	C/T	0.0554779	0.157039	intron-variant	RNFT2	GRCh38.p7	12:116794490	GCAATCCCAGCTACG[C/T]GGGAGGCTGAGGTGG	84900
rs150577051	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785530	CTCCTGGGCTCAAGT[A/G]ATTTTCCTGTTTCAG	84900
rs150581070	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844794	TCACTTAACCAAGTC[C/T]ATGTGAACAGGGGTT	84900
rs150634090	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116839157	TTAGCACTTATTCCA[A/G]TTGTTAACTAGGTAG	84900
rs150642173	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116750390	TGGGGGCTCCTCCTC[C/T]GAAGCCCAGGGAGAG	84900
rs150647298	in-del	-/TTTG	0.452842	0.146134	intron-variant	RNFT2	GRCh38.p7	12:116801805	TTCTGTGGGGTTTTT[-/TTTG]TTTGTTTGTTTGTTT	84900
rs150661326	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116769990	CAGTAAGCCAAAATC[A/G]TGCCACTGCATCCAG	84900
rs150696631	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802050	TGGTTTTGAACTCCT[A/G]ACCTCAAGTGATCCA	84900
rs150717658	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825654	CCTTGTGGGAACATT[C/T]ATACCACAGAAATTG	84900
rs150784938	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813290	GCTTGCCTGGCCTTC[A/G]CCTCTCTTCCCAGCC	84900
rs150823687	snp	C/T	0.0410537	0.137264	intron-variant	RNFT2	GRCh38.p7	12:116745277	CCTCCCCGGTTCAAG[C/T]GATTCTCCTGCCGCA	84900
rs150838801	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116827615	AAAGTTTTATTGGAA[-/C]CACAGCCACACCCAT	84900
rs150841176	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116786693	CTGTGGTTGCAGTAA[C/G/T]GAAATACCACAAACT	84900
rs150855526	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778310	ATGGGTATGGATCCT[C/T]CATGAGTGGTTTGGT	84900
rs150860379	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116835574	ATCAGCCATTGGGGC[A/G]TACTGATTACTTGCT	84900
rs150876261	snp	G/T			utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740404	AGACGAAGAGGAGGG[G/T]GAGGCCTGTCCTCTC	84900
rs150914845	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116831426	TATGTTTCCTTTCTT[C/T]ACCATAAAGTTGCTA	84900
rs150944853	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116787656	GGAGTTGAGGTTGCA[A/G]TGAGCCATGATCATG	84900
rs150965997	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780083	GTTCAGAAAGCTGAG[A/T]CATGTCCCAGGCATT	84900
rs150970683	snp	C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116837268	AGGGCCCACAGATCC[C/T]GTCCCCTCCTCTGGA	84900
rs150978264	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742670	GAAGGAAGGGCCATG[C/T]AGTGACTCACGCCTG	84900
rs150980888	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116800424	GATCACCTGAGGTCA[C/T]GGGTTCAAGTCCAGC	84900
rs150990433	snp	C/T	0.0599851	0.162463	intron-variant	RNFT2	GRCh38.p7	12:116850295	AAGTAGCTGGGACTA[C/T]AGGTGTGTGCCACCA	84900
rs151017182	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833119	AGTTGGGGGTTCGCC[A/G]TGTTGGCCAGGCTGG	84900
rs151034388	snp	C/T	0.0637235	0.166737	intron-variant	RNFT2	GRCh38.p7	12:116796136	GTAGTCTTGAACTCC[C/T]GACCTCAAGTGATCC	84900
rs151112394	snp	A/G	0.0310518	0.120672	intron-variant	RNFT2	GRCh38.p7	12:116846566	AAGTGCTGGGGTTAT[A/G]GGCATGAGCCACTGT	84900
rs151158084	snp	C/T	0.0298908	0.118541	intron-variant	RNFT2	GRCh38.p7	12:116761263	AAGCAATTCCTCTGC[C/T]TCAGTCTCCCCAGTA	84900
rs151159612	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116840328	AAGAATCAGGCTCAG[A/G]AAAACAAAGGGATGG	84900
rs151162204	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116817276	CCTCAGCCTCCCAAA[C/G]TACTGGGATTACAGG	84900
rs151176583	snp	C/T	0.0260105	0.111035	intron-variant	RNFT2	GRCh38.p7	12:116807906	ACTCCTGGGCTCAAA[C/T]GATCCTCCCACCTCA	84900
rs151179707	snp	C/T	0.0178098	0.0926698	intron-variant	RNFT2	GRCh38.p7	12:116751903	TCCACCTGCCTTGGC[C/T]TCCCAAAGTGCTGGG	84900
rs151193570	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771174	AGACGTTAAACATGT[C/G]GATAGTCCAGGTGCG	84900
rs151230025	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116803704	ATGGAATGAAATCAC[C/T]ATCCCCCAGGATGTT	84900
rs151239492	in-del	-/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116851065	TCATCCTCACAACAG[-/C]CCCTGTGATGGGGGA	84900
rs151246961	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116768435	ACAGTCATGTGTCAC[A/G]TAATGATGTTTCTGT	84900
rs151250849	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826561	TGCCCAGTTTTCCTT[A/G]GTGGTTTGATCTCCT	84900
rs151279370	in-del	-/ATAGAGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116845273	AATATATATATATAT[-/ATAGAGAGAG]AGAGAGAGAGAGAGC	84900
rs151317531	snp	A/G	0.0142736	0.0832652	intron-variant	RNFT2	GRCh38.p7	12:116815368	TATCTTACAGTTCTG[A/G]AGGTCAGATGTCCAA	84900
rs180672739	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827805	GAAGTTTGGGATTTG[G/T]CCCAGAAACCAGCCT	84900
rs180690382	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116846625	TTAAAAAAACATTTT[A/G]TTTAGATTTTTTTAT	84900
rs180740743	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116792589	GATGATTATTTTATT[C/T]GGTGAGATTAATGTG	84900
rs180744893	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116747934	GGTGGCTCATGCCTG[C/T]AATCCCAGCACTTTG	84900
rs180746533	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116770198	GATAGTAAGTGTCCT[A/G]TATGGGTGTATCTTT	84900
rs180753248	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816524	GTGAGAGGGAGAAAA[C/T]GACACATTTTCATCA	84900
rs180764839	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803804	TGAGACCTCAGTCTC[C/T]ACTGGAACCTCAACA	84900
rs180767393	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758944	TCCTCGATTATTCCC[C/T]CAAATATGTTTTCCA	84900
rs180773456	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116838106	CTCTATCTTAGAGAT[C/T]GCTCCTTATCCTATT	84900
rs180782688	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116782919	AAATAGCACAGGTAT[G/T]AAACTCTTCAGTTAC	84900
rs180962952	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796348	TCTGAATAACACAGC[A/C]TTTGACCAACTTGCC	84900
rs180979170	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841856	ATATAAATATATATA[A/T]AAATATATATATAAA	84900
rs180980403	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116743721	TCCCATACCCCCTGC[A/G]ACTCTGGGGTTGGCT	84900
rs180984945	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116764721	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	84900
rs180984976	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116820754	ACTGTCTAGCAACTT[C/T]GAACAACATACCCTG	84900
rs181010755	snp	A/C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116809819	CTGGGACTACAGGCA[A/C/T]CCACCACCACGCTCA	84900
rs181011078	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787074	GACATGATTATTTTC[G/T]AAATAATGTCACATT	84900
rs181020421	snp	C/T	0.0115144	0.0749975	intron-variant	RNFT2	GRCh38.p7	12:116851608	AGCCGGGCGCGGTGG[C/T]GGGTGCCTGTAATCC	84900
rs181035562	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116833716	ATGTCATCACTGCCC[A/G]GGGCGGGGGGCCCCC	84900
rs181065920	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116752464	TGTTTTTTAATCAAA[A/G]AGAAGAGTACCAAAA	84900
rs181071011	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116776329	CTTCAAGATAAAATG[A/G]AAAGGATAAGTCAGA	84900
rs181157778	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832352	CTTCTTTGATTCGAC[A/G]TAATGTTTGTGACAT	84900
rs181166291	snp	A/G	0.021333	0.101051	intron-variant	RNFT2	GRCh38.p7	12:116850814	TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTC	84900
rs181313181	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742331	AGAATGCAGTGGCAC[A/G]ATCTCGGCTCACTGC	84900
rs181315340	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116841981	GAGAGAGAGAGAGAG[A/G]GAGAGGGAGGATCCA	84900
rs181412493	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763568	GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA	84900
rs181423154	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116808845	CGTCCTGTGCTCCCC[C/G]TGGCTCCCCCACTCT	84900
rs181430991	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785950	CCAGCTACTCAGGAG[A/G]TTGAGGTGGGAAGAT	84900
rs181439025	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116832063	TTGAACCTGGGAAGT[C/T]GAGGCTGCAGTGAGC	84900
rs181478004	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116841909	AATATATATATATAA[A/C]TATATATATAAAAAT	84900
rs181481118	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116741888	ACTCCTGGGCTCAAG[C/T]GATCTTCCTACCTTG	84900
rs181516678	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753238	TCACTGCAGCCTCCC[C/T]ATCCTGGGTTCAAGC	84900
rs181533211	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116797959	AACATGGCATACTGT[C/T]GGGCATGGCTTATGG	84900
rs181618293	snp	C/T	0.0901694	0.192235	intron-variant	RNFT2	GRCh38.p7	12:116782073	GACAGAGCGAGACTC[C/T]GTCTCCAAAAAAAAA	84900
rs181632367	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116757738	GGCTCGTTTTGTGGC[C/G]TATCATATAGTCTAT	84900
rs181632737	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802307	CCCTTTTATTGAGGA[A/G]CACAGCATCTTGCAG	84900
rs181643370	snp	A/C	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116845817	CCTCTCTCCCCTGCA[A/C]CCCCAACTACAGCCA	84900
rs181645514	snp	A/C	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116826839	AATATACCCAGAGTC[A/C]AATTATCTTCTCCCG	84900
rs181690612	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738241	GTCCTAGCGCCGGAC[C/T]CGGCGACGCCAAGAA	84900
rs181696507	snp	C/G/T	0.00358891	0.0422285	intron-variant	RNFT2	GRCh38.p7	12:116777662	GGGTGGATAAAAGTA[C/G/T]CTGCCTCATAATGTT	84900
rs181699321	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116821741	ATGCAGATTCCTGGC[C/T]CTGTGCTAGCTTGCT	84900
rs181890331	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768943	GCCATATTGGCCAGG[C/T]TGGTCTCAAACTCCT	84900
rs181893836	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792862	ATCCACTGAGAAGGT[A/G]GGTTGGTTTTAATAT	84900
rs181901983	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116838644	TCCCTAATTATGAGC[A/G]TGGTTGAGCATCTTT	84900
rs181904910	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116817115	CCTTCTGGGTTCAAG[C/T]GATTCTCATGCATCA	84900
rs181953040	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116771188	TGGATAGTCCAGGTG[C/T]GTTGGCTCACGCTGT	84900
rs182047421	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772486	TGATTTTTGTATTTT[C/T]AGTAGAGACAGAGTT	84900
rs182057088	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818557	GCTGCTGGCAAGTGA[C/G]TTGTGAAGCCTCTAA	84900
rs182062360	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116794600	GAGACTTTGTCTCAA[A/G]AAACAAAAGAAAGGA	84900
rs182109617	snp	C/T	0.00709101	0.0591204	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750123	CCATGGCGGCCACCG[C/T]GGGGGCTCCCTGCTG	84900
rs182123762	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737704	GAAAAAAGGAGGAAG[A/G]TAACGAAGGAAGGAA	84900
rs182157481	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116781335	TCAGCTTCCAGTTGG[C/G]TTCAGCTGATGGGAA	84900
rs182166461	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116826070	CTCTCCTCCCTTCCT[C/T]CCCACCCCCACAAGT	84900
rs182172004	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748336	CTCCGCCAGCAGTGG[C/G]TCTGCAAGAGCTACA	84900
rs182183967	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116747435	TACTCAGGAGGCTGA[A/G]GTGGGAGGATCACTT	84900
rs182251940	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116822771	CTTTGGGAGGCTGAG[A/G]CGGGCAGATCACCTG	84900
rs182259920	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116842770	GTAGGGACGGGGTTT[C/T]GCCATGTTAGCCAGG	84900
rs182316908	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798681	TGAAGTGATTCTCCC[A/G]CCTCAGCCTCCTGAA	84900
rs182345357	snp	A/T	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116845450	GGAATCGGGGCAACA[A/T]CATAAAACAGGGGAG	84900
rs182373537	snp	C/T	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116840607	CACCTACCTCTGACT[C/T]CTCCATCCAGTCATC	84900
rs182404345	snp	C/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116757348	TGATCTTGGTTATTT[C/G]CTTTCTTCTGCTGGG	84900
rs182437613	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116800775	GCTGAGATTGTGCCG[C/T]TGCACTCCAGCCCAG	84900
rs182485647	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778004	TTAGTGAGACACAGT[A/G]AGCAAAGAGCTTAGC	84900
rs182500955	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798260	CAGCAGCAGCAAATA[C/T]ATGTGCGTGTTCTTT	84900
rs182513093	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822352	TCTCTCTCTGTCTCT[C/G]TCTCTCTCTGTGGCA	84900
rs182558654	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116753781	AGGGACCTAAATCCT[C/G]TCCCTAAGTCAGAAT	84900
rs182585858	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852560	ATGTGAATGCAGCTG[C/T]TCTGTTCTCCCTACC	84900
rs182634024	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812868	GAGGAGGAAACCATC[A/G]TTCCAAGAGTTTCAG	84900
rs182664029	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853479	GTTAGGAAGACATCC[A/G]GGCTGCTGAGACTCG	84900
rs182667448	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739319	GGGAACTGGGAGACC[C/T]ATAGATGTTTTATTC	84900
rs182718917	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778307	GTCATGGGTATGGAT[A/C]CTCCATGAGTGGTTT	84900
rs182858711	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116810658	GGTGCTGGGGGAATT[A/T]ATCATCAAGCTAAGG	84900
rs182864070	snp	A/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116789247	AGTAGATGGATGGGT[A/G]GATGGGTAAATGGGA	84900
rs182865757	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116834179	GCTGGAGTTCGGTAG[C/T]GCAGTCTCGGCTCAC	84900
rs182884215	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116852114	TGGCACAGGTGACCA[C/T]GCAGAAGCCACCAGA	84900
rs182934012	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836091	GAAACAGCAGCGACC[C/G]CTTCCTCAGCCCACA	84900
rs182940427	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116765016	CTCTGTATCCATGGA[C/T]GGGCCTCCAGGGGTC	84900
rs182942425	snp	C/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116745136	TGGGGCTTGGTGAGG[C/G]AGGGAATCCAATCGT	84900
rs182942905	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744612	GCACATTTTGGCTGC[C/T]TAGTGTCTGAGCAGA	84900
rs182977375	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790092	TCTTATATTTGGTAG[A/G]TGTCAAAACACTTCT	84900
rs182989275	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835317	TACTGAATGTTTTCT[A/G]TCTCTCTTACCTCAA	84900
rs182992467	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754422	TCCACAATTTTAAAA[C/T]TGTGAATTGTGCTGC	84900
rs183081442	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116806480	TAAAGATGGTTGTTA[G/T]GGCCAGGCACAGTGT	84900
rs183095182	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829624	ATATAAAAGTTGGCT[A/C]TAAATCTCTGTCCAC	84900
rs183105421	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116848290	TTTGCTATTGTGAAT[A/G]GTGCTGCAGTGAACG	84900
rs183155028	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784305	ATCCGCCGCACGTGT[A/C]GTGTCCTCTTACAAT	84900
rs183158935	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841221	CTTTGGGAGGCCAAG[A/G]TGGGCAGATTGCTTG	84900
rs183160302	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818980	TCAAAGGGCTCATTC[A/T]CATCATGGAGGTCCG	84900
rs183160938	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116740284	CAACAATGTCCTAAG[A/G]CTTCTTAGCAGATTC	84900
rs183163468	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761199	TGTTGCCCAGACTGG[A/G]GTGCAGTGGCATGAT	84900
rs183230216	snp	A/C	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116794885	GTTTGCTTACAGGGG[A/C]AATGCTAGATCCTGA	84900
rs183239136	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766505	TGCCTGGAGTTGGAC[A/C]GCTCCCACACAGGAT	84900
rs183245688	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116755095	GTTTTTCCAATGTTA[C/T]CTTCTAGAATTTTTA	84900
rs183255702	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116799132	AATCAGTTCTGTGTG[A/T]TCGTAGGACTTGAGG	84900
rs183258516	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844126	CACTCTGGTTCTTTC[A/G]TGAGTATACAGTGGA	84900
rs183276905	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811964	GCCACTAGCTATATA[C/T]CCTCGGGTGAGTGAG	84900
rs183328513	snp	C/T	0.0209421	0.100162	intron-variant	RNFT2	GRCh38.p7	12:116760164	CCTCACCCAGCTCCC[C/T]TGCAAAACGAAGGGC	84900
rs183339011	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739606	ACCAAGCCCTGCCAC[A/G]TTTAGAGGAGAAAGT	84900
rs183481618	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779098	CAGTTCAGCGCTCTT[G/T]CTACAGGTGATACTT	84900
rs183490494	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822904	TGGGAGGCTGAGGCA[C/T]GAGAATCACTTGAAC	84900
rs183576563	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772114	TTTTTATTTTGGAGA[C/T]ACAGTCTTGCTCTGT	84900
rs183585558	snp	A/C	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116817896	ATGAAAGAAACAGAC[A/C]AAAACAGAGTCCCTG	84900
rs183646327	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116775468	CCTTGGAGGCGACAC[C/T]TACCACTGAGCTTGA	84900
rs183651341	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751846	TCACTGCAAACCTCT[A/G]CCCACTGAGTTCAAG	84900
rs183661613	snp	A/G	0.0209421	0.100162	intron-variant	RNFT2	GRCh38.p7	12:116790376	CCCCTGTATTCGTGA[A/G]TTTATATCCTCTTAA	84900
rs183666384	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116767618	AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	84900
rs183733570	snp	C/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116840399	GATTCAAATCCAGAG[C/G]CTCTGATGCCATTGG	84900
rs183740824	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116745540	TGCTGGGATTATAGG[C/T]ATGAGCCACCATGCC	84900
rs183771295	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749017	ATCTGACACGTAGTA[C/G]GTTTCAATAAAGGTT	84900
rs183778112	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116835586	GGCATACTGATTACT[C/T]GCTGGTTCTGATCAA	84900
rs183783005	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116845446	GGATGGAATCGGGGC[A/G]ACATCATAAAACAGG	84900
rs183793454	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794074	AGTTCGAGACCAGCC[A/T]GGCAACAAAGTGAGA	84900
rs183834429	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116783323	CCCCTACACTGGCTT[C/T]GTGTTCTTGGGCTGG	84900
rs183844249	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828967	AGCCTGGGCAACATA[C/G]ATAGACCCCATCTCT	84900
rs183859117	snp	C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116751004	TTACTGCAACTTTTG[C/T]CTCCCAGGTTGGTTA	84900
rs183876439	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116824573	AGCAAGAGCACCAGC[C/T]ATCACATCCAAGTTC	84900
rs184027804	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773936	TAAACACCCTGCGGT[A/G]TGTACATACAGTGGA	84900
rs184030788	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116805084	TATCTTCAAGGTGTA[C/T]TAGAGACACATTATC	84900
rs184078831	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116799506	TGCTGGGTGCCCACC[A/G]CACTATCTCAGAGGG	84900
rs184086309	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116844525	CAGGCGTGAGCTACC[A/G]TGCCTGGCCATTATG	84900
rs184087817	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823691	CTGTCTAAAAAAAAT[A/G]ATAATAATAATTCTT	84900
rs184124432	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116762977	ATCCTAGCTACTCAG[G/T]AGGCTGAAGCAGGAG	84900
rs184149227	snp	C/T	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116756366	GGGTTGAGTTCTTGA[C/T]GTGATTCTCTACTTG	84900
rs184157321	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807530	AGTGACTTGCCTGGG[A/G]TATGTAAATGACAGG	84900
rs184158572	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779999	AAAGGGAATCTGGAC[C/T]GAAGCAGGTGGACTA	84900
rs184192537	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116767836	ACCTGCCTTGGCCTC[C/T]CAAAGTGCTGGGATT	84900
rs184205438	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790538	GGGAGCAGCCAGTGT[A/G]GGGCCAGCCTTTCAC	84900
rs184272299	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741171	CAAAACTGGATTGAA[A/C]AATACCTCACCCTCA	84900
rs184280610	snp	C/G	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116784760	CCTCCCCAGTGACGT[C/G]GGAGCCCATCCTCCT	84900
rs184287239	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830226	TGTTACTACTAACCT[A/G]AAGACCTCATTCACA	84900
rs184313376	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796137	TAGTCTTGAACTCCC[A/G]ACCTCAAGTGATCCA	84900
rs184316933	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116848772	TTAACGTCCCAACCC[A/G]CCCAAGCCCTCCCTG	84900
rs184323853	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820380	AGCCACCATGCCCAG[C/G]TATCCCTGTGTATTT	84900
rs184335399	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116832239	ACCTCTCACCCCAGA[C/T]GACCAGGGATCTGAT	84900
rs184355945	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850756	CCTCAGCCTCCCGAG[C/T]AGTTGGGACAACAGA	84900
rs184408609	snp	A/C/G	0.0444908	0.142359	intron-variant	RNFT2	GRCh38.p7	12:116763766	CCTGGGTGACAGAGC[A/C/G]AGACTCCATCTCAAA	84900
rs184413436	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808878	CCCCCAGCACTGGGC[C/T]GTTGGAAATCGACCT	84900
rs184420579	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736913	CCAGGAGGACACAGA[A/G]CCCCCAAATTAAACG	84900
rs184421272	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786278	AGACACGTGCCACCA[C/T]GCCTGGGTAATTTTT	84900
rs184431463	snp	C/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116780908	ATGTTCAGATCCCAG[C/G]CATACGCCTCTCCAG	84900
rs184530567	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116757104	CTAGGTTTTCTAGTT[C/T]TTGTGCATAAAGGTG	84900
rs184549534	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800521	GCCTGTAATCCCAGC[C/T]ACTCGGGTGGCTGAG	84900
rs184610898	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116785818	CTTTGGGAGGCCAAG[A/G]TGGGTGGATCGCTCG	84900
rs184622749	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116763414	ACTTCTGCACTGCTG[G/T]TGGGAATGTAAACTA	84900
rs184663149	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116747835	GCACGTCGAGCACAT[C/T]GGCTCCGCTTGCATC	84900
rs184665199	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116791972	GATTTGAACTCAGGC[A/G]GTCCTCCTGCTCCAG	84900
rs184691080	snp	A/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116838023	CAAACATATTTTTTT[A/T]AAAAAAAACATAAGT	84900
rs184768675	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841858	ATAAATATATATAAA[A/T]ATATATATATAAATA	84900
rs184813417	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769698	AAAAATGTTACAGTA[A/G]GCTAAGGTCAATTTA	84900
rs184821322	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116815447	TGGGAGGCTCCGGGG[C/G]ACAATCCATTTTCTT	84900
rs184833695	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116836722	CTGAGGTCAGGAGTT[C/T]GAGACCAGCTGGGCC	84900
rs184842577	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814398	GGGGAAGGGAGGGCG[A/G]TGCTCTTTTAGACAG	84900
rs184854014	snp	A/G	0.00438332	0.0466095	downstream-variant-500B	RNFT2	GRCh38.p7	12:116854034	GGGAAGCCTCTGAAG[A/G]CCCCAGATACCAGCA	84900
rs185092682	snp	C/G/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116746587	AGTTGGGATGGGGTA[C/G/T]GGGTTAGGGGAGACA	84900
rs185229808	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742199	AAGAAAGGCAAGGCA[A/G]GGGCAATAGTTTAGG	84900
rs185246213	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116819751	TCCTTTTTCTTTTGT[A/T]TTGAGGCATAACTTA	84900
rs185317584	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116816848	AAATAACAAATACTC[A/G]TGTACCCAGCTTAAA	84900
rs185321647	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792656	GTGAATAGTCTTCCC[C/G/T]AAGATAAATTGCAGG	84900
rs185331711	snp	C/T	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116827334	AAGGCTTTTCATAGG[C/T]GGTGACAGTTAGCTG	84900
rs185338042	snp	C/T	0.0182019	0.0936463	intron-variant	RNFT2	GRCh38.p7	12:116846203	TAATAATCATTATTA[C/T]TATCATAATAGCTAA	84900
rs185349709	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794990	TATATTAACTTAGCC[C/T]AAACCTTGGTAAGAA	84900
rs185353736	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751590	TGTATTTTTTAGTAG[C/G]GACGGGGTTTCACCA	84900
rs185375567	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738984	AGATGCTGCTGCTGA[C/T]CGGTTTGTTACCTAA	84900
rs185380464	snp	A/G	0.030665	0.119967	intron-variant	RNFT2	GRCh38.p7	12:116841606	TACAAAAATTAGCCT[A/G]GCATGGTGGCACACA	84900
rs185393945	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782141	ATACTAAAACTGGAA[C/T]GATACAGAGATTAGC	84900
rs185405499	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116770973	ACCCATTTTTATTAG[C/T]AACATTTTGCTGAAA	84900
rs185407185	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116748104	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	84900
rs185409335	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116758083	TTATATAATGTCCCT[C/T]TTTGTCTCTTTTAAC	84900
rs185411785	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802681	GCCCAGCCAACACTT[G/T]GATTTGGGCCCAAGG	84900
rs185491357	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116831001	CCTTAATTCTCTCCA[A/G]CCTCACACTCCTTGG	84900
rs185575826	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842137	TGCTGGTAGGATTCC[A/G]TTCCTAATGGGCTGT	84900
rs185579279	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822462	AGCTGCGTCACCTGG[A/G]GCAGGTTATCTAACT	84900
rs185609993	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116807927	TCCCACCTCAGCCCC[C/T]TGAGTAGCTGGGACT	84900
rs185617001	snp	G/T	0.0182019	0.0936463	intron-variant	RNFT2	GRCh38.p7	12:116850181	TTTTTTTGAGACAGG[G/T]TCTGGGTCTTCACCC	84900
rs185646064	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116778165	CTTTTGCCTCCTCTC[A/G]TAAAGCCTGTTGTGG	84900
rs185658648	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116754119	ATAAGCCACAAGCCA[A/G]GCACAGTCTTCCCGG	84900
rs185666748	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798320	AGTAACATTCTATAT[A/G]CAGCTCCCACGTTGC	84900
rs185696553	snp	C/G			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738155	CCTAAGGAACGGCGG[C/G]CTCCTATTGGTTAAG	84900
rs185705234	snp	A/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116757402	TCTCTAGTTCCTTGA[A/G]GGGTGACCTTGGAGT	84900
rs185730655	snp	A/G	0.00795532	0.062565	intron-variant	RNFT2	GRCh38.p7	12:116845564	ACTAAAGTTGGTTGG[A/G]AGGCTGTGAATAAGC	84900
rs185842569	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116781633	TTCATTGTCGCATCT[C/T]CTGATTCTCGCCCTC	84900
rs185853040	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116826126	TGCGTTCTTCCAAAA[A/C]ATTCTCCTCTCTGTT	84900
rs185946832	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116753408	TGCCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT	84900
rs185976544	snp	A/G	0.0119091	0.0762411	intron-variant	RNFT2	GRCh38.p7	12:116782971	CCTACTCACTCTACC[A/G]TGAGACTTCCCTCAT	84900
rs185981285	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827983	CTGGCCTGCAAGGAA[A/G]AACAGAGAGAGGGGA	84900
rs186041209	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739530	AACAGGGCAATATTA[C/T]GGGGAGTCAGGAGAA	84900
rs186057054	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116852276	GGAGAAATGGAGGAG[C/G]TTTGTAGCCACCTCG	84900
rs186098907	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838374	TTATGGGCATGCATC[C/T]CATTTCACACACACA	84900
rs186105604	snp	C/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116760011	TTCTGACCTCTCACT[C/T]TCCTTGGGCGGGTCT	84900
rs186120456	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116803980	AACTTTTGTCTTACT[C/G]AGAGCCTGGGGGAAG	84900
rs186130538	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116834678	TAGGTGCCCTTTTGT[A/G]TCTGGCACTTTCATT	84900
rs186206335	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116794092	CAACAAAGTGAGACC[C/T]TGTCTCTATAAAAAA	84900
rs186237385	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840485	TTACAAGATCAGAGC[A/C]CTTTTTCCAGAAATT	84900
rs186280799	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116749610	GGGACAGCAGTCACA[C/T]TGGATTGGGACCCAC	84900
rs186315754	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810046	TTCTGGGTCACATGA[C/T]TTGTTTTCTCATGCA	84900
rs186364107	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116772376	CTGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	84900
rs186367994	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116818202	GTGGCACACACCTGT[G/T]GTCCCAGCTACTCGT	84900
rs186391089	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788086	GCATGCGCCACCACA[C/T]CCAGCTAATTTTATA	84900
rs186394288	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116743729	CCCCTGCGACTCTGG[A/G]GTTGGCTACAGAATC	84900
rs186396290	snp	C/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116764758	TTAGCTGGGCATGGT[C/G]GTGGGCGCCTGTAAT	84900
rs186505593	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763906	ATACTTACATACTCA[A/T]GTTTATAGCAGCACA	84900
rs186527022	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809766	CAACCTCCACCTCCC[A/G]GGTTCAAGCTATTCT	84900
rs186528553	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851118	TATAGATGAGGAAAC[G/T]TGGGCACAGAGCTTG	84900
rs186585546	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116793105	GGCTTCCTGGCCAGC[C/G]AAGACGGGTTAAAGG	84900
rs186593719	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116838677	ATATGCTTCAGAGCC[A/G]TCTGTAGTTCCTTCT	84900
rs186593871	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817381	TCTCAAACTCCTGGC[C/G]TCTAGCAATCCTCAT	84900
rs186615371	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840757	CTGCTGGGCAGCTTG[C/T]AGGACTTTTTTAAGA	84900
rs186663827	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750350	GCCATGGGCTTCACA[A/G]GCAGGCTGCCTGCAG	84900
rs186681866	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772507	AGACAGAGTTTCACC[A/G]TATTGGCCAGAATGG	84900
rs186690811	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116818618	TTTGATGGCGACCCT[A/G]TCGGAGAGAGAAGGG	84900
rs186692165	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794660	GAGAAGGAAGGAAGG[A/G]AGGGAGGAAGGAAGG	84900
rs186728935	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116743041	AGCTATGATTGCACC[A/C]CTGCATTCCAGCCTG	84900
rs186741493	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833031	CAATTCTCCTGCCTC[A/G]CTTGAGTAGCCTCCG	84900
rs186763097	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777715	CGCAGGGTCTGTAAT[C/G]TGTCCATTATCTCAT	84900
rs186774622	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116821930	GCCTCTGCCTCCCGG[A/G]TTCAAGCCATTCTCC	84900
rs186990058	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848382	GTTCTATTCTCAACC[G/T]AGAAGGCGGAGGGAT	84900
rs186990996	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798072	GCCTGCTACCTCACT[A/G]GGACGGGCCCTGGTC	84900
rs187005992	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841920	ATAAATATATATATA[A/T]AAATATATATATATA	84900
rs187050542	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761391	GACCTCCGGTAATCC[A/G]CACACCTTGGCCTCC	84900
rs187055144	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116806713	TCATGCCACTATACT[C/T]TCCACCCTGAGTGAT	84900
rs187060597	snp	A/G	0.000172571	0.00928739	intron-variant	RNFT2	GRCh38.p7	12:116833969	CAAGGCTGGAGGGCC[A/G]GCCTAAGGAGGGCCC	84900
rs187063098	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784500	AAAAAACATGGCTGC[C/T]TAGGGAGGCTCTTTC	84900
rs187064600	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829981	TTTTTTTTTGCATTC[C/T]CTATTATTTCCATTT	84900
rs187098399	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752675	TTGAGGTCAGGAATT[C/T]GAGACCAGCCTGGCC	84900
rs187126803	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796527	TCTAAGCACAGGGAC[A/G]GGGAGGGAAGGTGGA	84900
rs187228200	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844556	TTTTAAATATGTCTC[C/T]GTTTCTATTTCTAAA	84900
rs187258004	snp	C/G	0.000290318	0.0120447	intron-variant	RNFT2	GRCh38.p7	12:116851916	GGCCTGTCAGCAGCT[C/G]CTGTGGACATTGCCA	84900
rs187281277	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116777132	CATGTTGGCCGGGCC[A/G]GTCTCAAACTCCTGA	84900
rs187292408	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799542	GTGAAAATGCAATTG[C/T]ACATCTCTTAGTATG	84900
rs187311368	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116824160	TGGCCAACCCTCCCC[A/G]TCTCACTCCTACCCT	84900
rs187385987	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771226	GCACTTTGGGAGGCC[A/G]AGATGGGCAGATCAC	84900
rs187546906	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116779401	CATGGATCATGCAGA[G/T]GATTCAGGGTGCCTT	84900
rs187550090	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811041	TCCACCATTTCCATC[A/G]GTATCACTTCCAGTC	84900
rs187551349	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116755334	CTGTTCCATTGGTCT[A/G]TGTCCCTATTTTTTT	84900
rs187561457	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116785423	TCAGCCTCCTGAGTA[G/T]CTGGGACTGCTCAGT	84900
rs187569192	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116830490	ACAAGATCTTGCTCT[A/G]TTGCCCAGGCTGGTC	84900
rs187602117	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745708	GTCAAATAAGTTTGG[A/G]GAACACTGGGCTTAA	84900
rs187613465	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741371	CCATACAGGCTGCTA[C/T]CACAAAAATATCATA	84900
rs187630286	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748429	ACTGCAGGTCTTCCA[C/T]AGGAACTAGAGATAA	84900
rs187633909	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767636	CCAGGCTGGAGTGCA[A/G]TGGCACGATCTCAGC	84900
rs187643817	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813004	TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCACG	84900
rs187645433	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116843187	CGGGAGGCACGACCA[G/T]GGGGCAGTTAACAAT	84900
rs187646854	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790428	TAACAGTCCCAGGAG[A/G]GTAGATGCTGTTGAT	84900
rs187841748	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116807596	CTGCCTCTCCCCGCA[C/G]CATTCCCCACTCGCA	84900
rs187890928	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819029	CCCTACGTGGGTAAT[C/T]TGGGGCAGATTCCTT	84900
rs187899097	snp	C/T	0.188	0.24219	intron-variant	RNFT2	GRCh38.p7	12:116841522	GGAGGGTGAGGCAGG[C/T]GGATCACCTGAGGTC	84900
rs187905912	snp	A/C	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116762978	TCCTAGCTACTCAGG[A/C]GGCTGAAGCAGGAGG	84900
rs188080784	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739830	TTGCACTGGGCAGCC[A/G]TTGGAGGGTTTAAAA	84900
rs188080981	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783348	GGCTGGCAACCCTAG[A/G]GGGATGCTTCTGGTT	84900
rs188089061	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760918	GAGTCTTGCTCTGTT[A/G]TCCAGGCTGCAGTGC	84900
rs188102774	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116811969	TAGCTATATACCCTC[A/G]GGTGAGTGAGTTCAC	84900
rs188108216	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853056	TGCCCTACCCTCTGG[A/G]GGAACGTCCCATCTG	84900
rs188134222	snp	A/G	0.00636936	0.0560724	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740393	CATCCCTCTGGAGAC[A/G]AAGAGGAGGGGGAGG	84900
rs188162766	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116767476	CACCTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT	84900
rs188238153	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752429	CATTTTATTTTTCAC[G/T]TGGCAGGTTTTTTTT	84900
rs188254570	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776111	CTGACAATAAAATAT[A/C]TCAGTCCATTAAAGT	84900
rs188271107	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796288	TGGGTGGTTACTAGG[A/G]CTGGTTGTATCAGAA	84900
rs188277799	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841848	AAATATATATATAAA[A/T]ATATATAAAAATATA	84900
rs188280820	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116820458	CCATAGCGACATGTG[A/G]CCAGTGGTTACTGGA	84900
rs188331619	snp	C/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116823264	AACACCCCCATCACA[C/G]AGAACACTGAGGCCC	84900
rs188366249	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116790171	TGCTAGAAAAGACCA[C/T]ATAGGGCCTTTGAAA	84900
rs188370898	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116786331	GGCCAGGCTGGTCTC[A/G]AACTCCTGACTTCAG	84900
rs188375283	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116832247	CCCCAGACGACCAGG[A/G]ATCTGATTTCTATTA	84900
rs188396823	snp	C/T	1.64879e-05	0.00287118	intron-variant	RNFT2	GRCh38.p7	12:116835940	GGTACATTTCAGCCA[C/T]CACCCTGCTCTCCTT	84900
rs188397623	snp	G/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116850799	TGCCCAGCTAATTTT[G/T]TTTTTGTATTTTTAG	84900
rs188402028	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744699	GCACAGCCTCTGTCC[C/G]CCTAAGGAATATTCT	84900
rs188443884	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116745289	AAGCGATTCTCCTGC[C/T]GCAGCCTCCTGAGTA	84900
rs188574589	snp	C/T	0.00914312	0.0669923	intron-variant	RNFT2	GRCh38.p7	12:116751593	ATTTTTTAGTAGGGA[C/T]GGGGTTTCACCATGT	84900
rs188622842	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116799200	AGCTCCTAGAAGCCA[C/T]GCTCCAGTCCTTGTA	84900
rs188625049	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844161	TCCAGAGGCTGCATC[A/G]CCTGCGAGGAGGTCA	84900
rs188640802	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798813	ACTCCTAAGCTCAAG[C/T]GATCTACCTGCCTCC	84900
rs188645031	snp	C/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116754916	TACAGATTGTGAAGA[C/T]TTTCTCCCACTCTGT	84900
rs188676357	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116766089	CCAGCCTGAGCCAAA[C/T]AGCAAGACTCTGTCT	84900
rs188777350	snp	C/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116756870	GGAGGGTTCCTTCTT[C/T]CTCTATCTTGTGGAA	84900
rs188787518	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780000	AAGGGAATCTGGACC[A/G]AAGCAGGTGGACTAA	84900
rs188816680	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116747841	CGAGCACATCGGCTC[C/T]GCTTGCATCTGTGGT	84900
rs188877350	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116774066	GGACATTAAGTGTAT[G/T]ATTTCACTTACATGA	84900
rs188878409	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853720	AGCCCTTCGCGGAGT[G/T]GGTGGTTGTCTTATG	84900
rs188883643	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116805812	AATTTATTCTTCCTC[A/G]GGGAAACCTCAGTCT	84900
rs188892388	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116847991	CAATTTATCCTGATG[A/T]TCTCCCTCCCCCAGC	84900
rs188893049	snp	A/T			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738171	CTCCTATTGGTTAAG[A/T]GCCGGGAAAGGGGGC	84900
rs188901230	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757441	GTGCTCTTTCAGTCT[C/T]TTTGATGTAAGCATT	84900
rs188916813	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836950	AAAAAAAAAGGACAT[A/G]ATAATAACAGCTACT	84900
rs188917053	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116781749	AAAGTCTCTTTTGCC[A/G]CAGAAGGTAACATTC	84900
rs188920321	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814433	GGGGGGTAGGGAGAA[A/G]GTAACATTCATGCAA	84900
rs188928968	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116778621	TTGGAAGGCTGAGGC[A/G]GGTGGATCACTTGAG	84900
rs188933061	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116822772	TTTGGGAGGCTGAGG[C/T]GGGCAGATCACCTGA	84900
rs188933461	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801847	GTTTTTTTGAGACAG[A/G]GTCTCACTCTGTTGC	84900
rs189094477	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116833079	GTGCGCCACCACGCT[C/T]AGCTAATTTTTGTAT	84900
rs189172523	snp	C/T	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116751075	GTGTGCCACCACACC[C/T]GGCTAAATTTTAAAT	84900
rs189174591	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116794901	AATGCTAGATCCTGA[C/G]AATATAAAAGTGAGT	84900
rs189176296	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116829320	TGACGGCCACCCCCT[A/G]CATCTCTGTACTCCA	84900
rs189288673	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771104	AATATTTGCTCTCTG[C/T]TTTTAAAGGAAAAGG	84900
rs189299362	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116816860	CTCGTGTACCCAGCT[A/T]AAAAAGTAGAGAACT	84900
rs189305863	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792757	TGGAGAAGAAAAGGA[C/T]GGGTTTTCATCTGCA	84900
rs189308902	snp	C/T	0.0252325	0.109451	intron-variant	RNFT2	GRCh38.p7	12:116838461	AGTTTTGACAGTTAT[C/T]GCTAAACTGCCCTCT	84900
rs189371271	snp	A/G	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116851387	GCACTCTTAACCTCC[A/G]CACTGCTCTGCCCCT	84900
rs189377766	snp	A/C/G	0.0923359	0.194016	intron-variant	RNFT2	GRCh38.p7	12:116763794	AAAAAAAAAAGGGGG[A/C/G]GGGGGGGGAAAGAAC	84900
rs189383667	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116795134	ATGAAGGCCGGGCCC[C/G]GTGGCTCATGCCTGT	84900
rs189384319	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831436	TTCTTCACCATAAAG[A/T]TGCTATTTCTTCAGG	84900
rs189396100	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841794	AAATATATATATATA[A/T]ATATATATATAAATA	84900
rs189427767	snp	A/C	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116741662	TTACAGGTTAGGTTT[A/C]TTTTTTGAGAGAGAG	84900
rs189449794	snp	A/G	0.0107246	0.0724382	intron-variant	RNFT2	GRCh38.p7	12:116785843	CGCTCGAGTTCATGA[A/G]TTCGAGACAAGCCTG	84900
rs189456121	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763507	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	84900
rs189463373	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116808830	GAAATTCTTGCTCCC[C/T]GTCCTGTGCTCCCCC	84900
rs189616524	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778167	TTTGCCTCCTCTCGT[A/G]AAGCCTGTTGTGGAC	84900
rs189631810	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754380	ATTTCTTTATACACC[C/T]GTTGATTGGTGGGCA	84900
rs189633786	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798392	ATAGAGAAAACACTG[C/T]ACAGTGGTTAAATGC	84900
rs189635082	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816012	AGTGTTTTGGGAAAC[A/C]GCCAGGCTTGGGCAG	84900
rs189646295	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842285	TCCTCCTTGTTGGAA[A/G]CAGGTCACTAGGCGC	84900
rs189653629	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822540	ACCTGCCTCATAGTG[C/G]TGTGCACAGAGTGGT	84900
rs189656254	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116819763	TGTATTGAGGCATAA[C/T]TTACATACTGTGGAG	84900
rs189733347	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742330	TAGAATGCAGTGGCA[C/T]GATCTCGGCTCACTG	84900
rs189740878	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769782	CATGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC	84900
rs189742246	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116774990	CAACAGGCCATGTGC[A/G]GTGGCTCACGCCTGT	84900
rs189897676	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116826177	ATCCTACTCTCCTTC[A/G]TTTCCCACCCGCTTC	84900
rs189918393	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116838069	CTATGCTGTTTTCTG[A/C]ACCTTCCTTTTTAAC	84900
rs189920017	snp	A/G	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116753657	TTAGAGAGGTGCGGT[A/G]ACTTGCCCAAGCTCA	84900
rs189940406	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116777781	ATTCCCATTTTATTC[A/T]TGAGAACCCTGAGGC	84900
rs189948646	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746813	ATGGGAAGGAACACA[G/T]AATGGGAAGCCCTGG	84900
rs189957410	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116790756	GAGCCCAGGAGTTCA[A/G]TACCAGCTTGGGCAA	84900
rs189981914	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792054	AATTCCTTTGGAAAA[C/T]TTTCTTTTTTGTTTT	84900
rs190145717	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845766	ATCCAGTATGGTCTT[C/T]GCGGCTCTGTGTGGA	84900
rs190151881	snp	A/C	0.0314385	0.121371	intron-variant	RNFT2	GRCh38.p7	12:116843512	AAAAAAAAAAAAAAA[A/C]AAACCCCAAGAAACA	84900
rs190161021	snp	C/T	0.000573641	0.0169261	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749865	CCAGGCGCTCAGCTC[C/T]GAGGCGAGTGTGGAT	84900
rs190167122	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116803752	CAACTTGAGGTGTAT[A/G]TAAAAGTCATCTGGA	84900
rs190177503	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116782343	GGGCAAGATAAGCCT[A/G]CTGGCGAGACACTCT	84900
rs190186268	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116772463	AGGCATGTGCCACCA[C/T]GCCCGGCTGATTTTT	84900
rs190188385	snp	C/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116827558	CAGGTCAGAAAACTA[C/T]AGGCTACAGGCCAAA	84900
rs190193858	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768529	TACCTAGTGATATTG[C/T]AGCCATCATAACGCT	84900
rs190198581	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116846343	AGTGGCATGATCATA[A/G]CTCATACAGCCTCAA	84900
rs190209629	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116800773	GAGCTGAGATTGTGC[C/T]GTTGCACTCCAGCCC	84900
rs190223830	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116845447	GATGGAATCGGGGCA[A/G]CATCATAAAACAGGG	84900
rs190269526	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757175	TCACTTGAAATATCT[C/T]CTGTTTCGTTTCTTA	84900
rs190398421	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116847534	TCTCTCTCTCTCTCT[C/T]TTTTTTTTTTGAGGC	84900
rs190441826	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781292	GGGGCTGACCTGCGC[A/G]AACTATATCAATGGG	84900
rs190442423	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116850266	CCCAAGCCATCCTCC[C/T]GCCTCAGCCTCCCAA	84900
rs190448063	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116777274	GGGAAGACAACATGA[A/G]TTAAGACATATAAAA	84900
rs190448277	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825376	TAGTTCACCTTAGTT[A/C]ATTTGAACCTGCATT	84900
rs190451939	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116821403	CAGCTCATTAGCCCA[A/G]CCCTTCAAGCCTCCA	84900
rs190532374	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737604	AAGATAAGGAAGGAG[A/G]GGAGGTAGGAAGAAG	84900
rs190554466	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783396	ATCTGCTCAGGCCTC[A/T]CTCCCTTGTTAGATA	84900
rs190556581	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740021	GACCAGCCTGGCCAA[C/T]ATGGTGAAATCCCAT	84900
rs190560969	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760954	CATGACCATAGCTCA[C/T]TGTAGCCTCCAACTC	84900
rs190565926	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116806164	GGTGGGCAGATCACT[A/C]GAGGCCAGGAGTTCG	84900
rs190569983	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839349	AGGATGGATGGGATG[A/G]TTGGATGGAATGTTT	84900
rs190585250	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829576	CCAAGGAATCCTCTT[C/T]TGAGTGACATGTGCC	84900
rs190686949	snp	A/G	0.0494327	0.149241	intron-variant	RNFT2	GRCh38.p7	12:116797729	CAGTGTTACAGCACC[A/G]TGACTACTCCTGCAG	84900
rs190718246	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841892	ATATAAATATATATA[A/T]AAATATATATATATA	84900
rs190765531	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116752980	GAATTCCAAGATTGT[A/G]GCTTGGCAAACAGTG	84900
rs190774186	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743173	TAAATAACTTTGGCC[A/G]TTAGTTTGGCCCTGT	84900
rs190774571	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787028	GGCAGGGTAACCTCC[C/T]CATGCCGATATCCTT	84900
rs190804321	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116834880	TTTTAGACCGAGTCT[C/T]GCTCTGTTGCCCAGG	84900
rs190810717	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852425	TGGTACCCAGCAAGA[C/T]GTCTGTTCCAGGGCA	84900
rs190857470	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748188	GAGCAAGGCTCTGTC[C/T]CAAAAGAAAAAAAAA	84900
rs190939713	snp	C/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116809803	TCAGCCTCCTGAGTA[C/G]CTGGGACTACAGGCA	84900
rs190941798	snp	A/G	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116804722	ACGCCTGTAATCCCA[A/G]CATTTTGGGAGGCCA	84900
rs191021606	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116766117	TCTCTAAAAAAAAAT[A/T]AAAATTTTTTTTTAA	84900
rs191029889	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798181	AAATAGCCACCTACA[A/G]GCCAAGGAGAGAGAG	84900
rs191043302	snp	C/T	0.000179905	0.00948261	intron-variant	RNFT2	GRCh38.p7	12:116851946	ATCCCCTCTGGTAGC[C/T]TTCAGAGCAAACAGG	84900
rs191104410	snp	A/C	0.0588605	0.161139	intron-variant	RNFT2	GRCh38.p7	12:116744239	TCAAAAAAAAAAAAA[A/C]AAAAGAGTTGTTTAT	84900
rs191108433	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116810577	TCACGTTCTTGGCTC[C/T]GAGACCCACCCTGAC	84900
rs191117564	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116788666	AGTTTGTTTGTTGAT[C/G]GATCATCAGTATCTG	84900
rs191130336	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116834019	AGGGGGCTCCTGGGC[A/C]ACCTAGAATACCCAT	84900
rs191181702	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116828272	ACTCGGGTCACCTGG[A/G]GACCTTATTAAATTG	84900
rs191187243	snp	A/G	0.00795532	0.062565	intron-variant	RNFT2	GRCh38.p7	12:116745529	GCCTCCCAAAGTGCT[A/G]GGATTATAGGCATGA	84900
rs191251286	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116745087	CCAGTGGAGGAGGAG[C/T]GCATATTTCCTGGGC	84900
rs191267290	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116822332	CAGGAGAAACAGGGT[C/G]TGTCTCTCTCTCTGT	84900
rs191277214	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800165	CCCCCTACAGTCTGC[A/G]GAACCATGAGCCAAG	84900
rs191302048	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116824406	TAGTAACAGCAAAGA[A/G]TCCAAAATAATAAGA	84900
rs191312862	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845023	CAAGGTGGGAGGATC[A/T]CATGAAGCCAGGAGT	84900
rs191317562	snp	A/C	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739122	TCAACAGCCAATAAT[A/C]GTGCCCTAAACTGAA	84900
rs191431791	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116741530	TTGCTATGTCTTAAT[A/G]TGGTGAAGGGAAAGG	84900
rs191432178	snp	C/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116773511	GTTCACTGGCAGTCT[C/G]TGTTTCTCCTTTAAA	84900
rs191432516	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116840489	AAGATCAGAGCACTT[C/T]TTCCAGAAATTCCTG	84900
rs191442329	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750810	GTGTATATATATATA[A/T]TATATATATTATATA	84900
rs191450503	snp	C/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116794814	TTCCCACCGCATGGA[C/G]TTCGGCTCGGCCACT	84900
rs191458617	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116841055	TCACTACAAAGTCAG[A/C]TGCTTTTAGTATCAG	84900
rs191462234	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818895	GTTACCACTGTTTAC[A/G]CCAGAGCAAGGAGGA	84900
rs191487721	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116793248	GCAGGGTTTCATTGT[A/C]CAGGCTGGAGTGCAG	84900
rs191488070	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116758617	TTTCCTTCATATATG[A/G]TTGTTAGTTTCACTG	84900
rs191521170	snp	A/C	0.0554779	0.157039	intron-variant	RNFT2	GRCh38.p7	12:116794521	GAGGATTGCTTGAAC[A/C]CGGGAGGGGGAGGCT	84900
rs191557533	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748742	GGTCCTTGGGATCCC[A/G]AGGTAATTCTAGAAT	84900
rs191738235	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841950	AAATATATATATAAA[A/T]ATATATATAGAGAGA	84900
rs191756779	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811740	ACCCTCATGACCCTC[A/G]TGGAAATCCAGGCCC	84900
rs191761919	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817818	TTCTTTGCATTTACT[A/C]CAAAAATATTTCAGT	84900
rs191781588	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116848094	GAGTGAGAACATGTG[A/G]TGTTTGGTTTTCTGT	84900
rs191783526	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807391	AATAAATATCCAGTG[A/T]CCCTAGTACTGGTCT	84900
rs191793182	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830102	ACTTAAAGAAAAGTT[A/G]CAAAAGTAATGCTGC	84900
rs191799553	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775048	GGGCGGATCCCCTGA[A/G]GTCAGGAGTTTGAAC	84900
rs191802242	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751716	TAGTATACTGTTATT[G/T]TTATTATTAATCTTA	84900
rs191813133	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116848502	CTCACAATGGCCCAC[A/G]AGTACCTACACCATA	84900
rs191815635	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795600	AAATGGCTCACGGCT[A/G]CTAGGGTAGACAATG	84900
rs191830073	snp	A/G	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116771751	TCTACGCAATGTGGT[A/G]GGGCAAGTGGGGAGG	84900
rs191831071	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116760129	TGTCAGGGAAGTGGG[A/G]GAAAGCTGGCAGTCA	84900
rs191965403	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822900	TACTTGGGAGGCTGA[A/G]GCACGAGAATCACTT	84900
rs191979290	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116850502	TAACTTAGTACCTAG[C/T]ACCTAGGACTTGATG	84900
rs192043169	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789423	AATGGTAGGAGAGTG[A/G]TGGGTGGATGGATGG	84900
rs192125192	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739537	CAATATTACGGGGAG[C/T]CAGGAGAATGAGAAG	84900
rs192131413	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783079	GATGCTTTTAAATCA[C/T]TACTATGCCCATCTT	84900
rs192187826	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835986	CTGTGGACGTGTGGG[C/T]GGAGTTAGGAAAGCC	84900
rs192244923	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116790372	GAAACCCCTGTATTC[A/G]TGAGTTTATATCCTC	84900
rs192317700	snp	C/T	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116843555	AACAATCCAGGGCCA[C/T]CTGCCTTCCCCACTG	84900
rs192319443	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779667	ATGTTAGCATGCCCC[A/G]GGACCTGCTTCTCCC	84900
rs192326196	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116756015	ATGCCTCCAGCTTTT[C/T]CTTTTTGCTTAGTCT	84900
rs192333271	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799269	ATTCTTGTGTCTGAC[A/G]TTTCTCTGACTTCCT	84900
rs192344506	snp	A/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116823687	GACTCTGTCTAAAAA[A/T]AATAATAATAATAAT	84900
rs192424109	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849874	TTTAAAACAAGGTCT[C/T]GCTCTATCACCCAGG	84900
rs192486131	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763257	TATACAAATGGCCAA[C/T]AAACTTATGAAAAAA	84900
rs192498043	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116767665	GCTCACTGCAATCTC[C/T]GCCTCCCAGGTTCAA	84900
rs192512468	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813933	TAGTATTCATGATGT[G/T]AAGATTAAACAGGAC	84900
rs192517854	snp	C/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116807828	TTTTGTTTTGAGATA[C/G]GGTCTTGCTGTGTCA	84900
rs192521476	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116790522	ACAAACTTATAGCAG[C/T]GGGAGCAGCCAGTGT	84900
rs192523297	snp	C/T			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836572	TTTCAGCAGCATTCT[C/T]GACCCCCTGTGGGTC	84900
rs192546551	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853927	CATCTCAGAGTTTGT[A/C]CCATCCCACAAAATA	84900
rs192580599	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853195	GCAGCCAGGAGTCCC[C/T]GTTGGAAAAGAACAA	84900
rs192588831	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780815	CATGCAGGGTTCCAG[A/G]TCGGCACCACGCACT	84900
rs192590330	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746481	CAGTGAGAGCAAGGA[A/G]CAGGGGACTGTCATT	84900
rs192665080	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116767512	ACAGGTGTGAGTCGC[C/T]GCACCTGGCCCCGAA	84900
rs192667575	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116812031	ATGACTGATGATGTT[A/G]CCTGGCTCCAGGAGG	84900
rs192712291	snp	C/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116784585	CAAGAAGGAACTCAG[C/G]ATCTTCCCCAAAGCC	84900
rs192727254	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820051	TGTTTTTCTAAGACT[A/T]TGAAATTCCTTGTTT	84900
rs192753408	snp	C/T	0.00159617	0.0282053	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740415	AGGGGGAGGCCTGTC[C/T]TCTCTGGGATCCATT	84900
rs192769331	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116830646	GCGGTCGCTCACACC[C/T]GTAATTTTAGCACTT	84900
rs192804036	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116785475	TTTTTAATTCTTCTT[C/G]GGGATGGAGTCTCAC	84900
rs192839394	snp	G/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116841558	TTCGAGACCAGCCTG[G/T]CCAACATGGTGAAGC	84900
rs192873372	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794909	ATCCTGAGAATATAA[A/G]AGTGAGTAAGACATC	84900
rs192874885	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751381	ATACTCAACAGTCAA[G/T]AATTGGCCTCTAGTA	84900
rs192931515	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841798	ATATATATATAAATA[A/T]ATATATAAATATATA	84900
rs192958496	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116814622	AACTTCATGGGCAAG[C/T]ACCCTTTGCAGAAGG	84900
rs192959003	snp	C/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116762639	GGCTGGAGTGCAGTG[C/G]TGCAATCTCGGCTCA	84900
rs192998080	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844237	TTTTTTGTTTTGTTT[C/T]ATTTTGTTTTTCAGA	84900
rs193040393	snp	A/C	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116819737	TCTCTTGCCTTTTTT[A/C]CTTTTTCTTTTGTAT	84900
rs193084456	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774794	GGTGGAGGGTGGAGG[G/T]GATGGAGGGTGGAGG	84900
rs193123839	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116779091	TGACTCCCAGTTCAG[C/T]GCTCTTTCTACAGGT	84900
rs193180672	snp	A/T	0.0049977	0.049738	intron-variant	RNFT2	GRCh38.p7	12:116838022	ACAAACATATTTTTT[A/T]AAAAAAAAACATAAG	84900
rs193201944	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116791651	ATTCCATTGTGTGGA[G/T]AGACTACAATTTGTT	84900
rs193275761	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116799097	AAGTCTACTTCCAGG[C/G]TCATTAAGGTTGTTG	84900
rs193276872	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116755084	TGTCTAGAAGGGTTT[C/T]TCCAATGTTATCTTC	84900
rs199499363	in-del	-/CA			intron-variant	RNFT2	GRCh38.p7	12:116769901	TAGCCAGGTGTGGTG[-/CA]GCAGGATCCTGTAAT	84900
rs199510882	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741529	TTTGCTATGTCTTAA[G/T]GTGGTGAAGGGAAAG	84900
rs199536887	in-del	-/T	0.0349115	0.127424	intron-variant	RNFT2	GRCh38.p7	12:116796095	GTATTTTTAGTAGAG[-/T]AAGGGTTTTCACCAT	84900
rs199539227	snp	C/T	1.65094e-05	0.00287305	intron-variant	RNFT2	GRCh38.p7	12:116754101	CTGTGGCTGCTGCAA[C/T]AAATAAGCCACAAGC	84900
rs199555935	snp	A/G	0.000425411	0.0145782	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737810	TGAAGGTGCTGCTGA[A/G]GAAGTAGACGAGCGA	84900
rs199574468	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116849071	TGATCCGCCCATCTC[A/G]GCCTCCCAAAGTGCT	84900
rs199580893	snp	C/T	0.00121008	0.0245678	intron-variant	RNFT2	GRCh38.p7	12:116851863	TCTTTATGTCTTTCT[C/T]CTCTTCCTATTCTGT	84900
rs199589629	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842899	TTATAAGGGGTAGTG[A/G]CTCATAACTGCCTGT	84900
rs199590354	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808690	GCCACATGGCCCCCG[C/T]AGTTTAATTTCCTTT	84900
rs199608888	snp	A/C	0.000268451	0.0115825	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750166	GGGGACCACCGGGGG[A/C]ACTCGGAGGAGGGAG	84900
rs199648688	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116831548	ACTTTTTTTTTTTTA[A/C]TATTACAAAGAATGC	84900
rs199657033	snp	A/T	0.184203	0.241186	intron-variant	RNFT2	GRCh38.p7	12:116766123	AAAAAAAATAAAAAT[A/T]TTTTTTTAATTAGCC	84900
rs199672654	snp	A/T	0.000594099	0.0172249	intron-variant	RNFT2	GRCh38.p7	12:116754105	GGCTGCTGCAACAAA[A/T]AAGCCACAAGCCAGG	84900
rs199800369	in-del	-/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738386	TAAAAAGAGAACGCG[-/T]ATTTTTTTTTCTTTT	84900
rs199815064	in-del	-/TA	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116767053	CCTGCTGTTACTACT[-/TA]TATATATATCTAGAC	84900
rs199818565	snp	A/G	0.0501905	0.150254	intron-variant	RNFT2	GRCh38.p7	12:116827231	TCTCAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	84900
rs199859955	in-del	-/CTT			intron-variant	RNFT2	GRCh38.p7	12:116835297	AAGCTCCCAACCACA[-/CTT]CTTCTACTGAATGTT	84900
rs199882634	in-del	-/TAAAATAAAA			intron-variant	RNFT2	GRCh38.p7	12:116800813	AGCAAGACTCCATCT[-/TAAAATAAAA]TAAAATAAAATAAAA	84900
rs199882799	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116843705	TCCTCAGCTGGGCCC[C/T]GGGGTAAACCTGGTT	84900
rs199921921	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116763604	AACCCCATCTCAGTT[-/A]AAAAAAAAAAATAAC	84900
rs199924090	snp	G/T	0.18325	0.240924	intron-variant	RNFT2	GRCh38.p7	12:116850635	CTTTTTTTTTTTTTT[G/T]TTGTTGTTGTGAGAC	84900
rs199937412	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116780670	AAAATGGCATAAAGA[A/C]AAAAAAAAAAAAAAG	84900
rs199941109	in-del	-/AAAAAATATATAT			intron-variant	RNFT2	GRCh38.p7	12:116806377	TGTCTCAAAAAAAAA[-/AAAAAATATATAT]ATATATATATAGATA	84900
rs199952382	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753154	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	84900
rs199977367	snp	A/G	0.000115343	0.0075933	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779207	CAGCCTCATATTCCT[A/G]AAGCCCAACCTGGAG	84900
rs199982214	in-del	-/AATGGGTA			intron-variant	RNFT2	GRCh38.p7	12:116788874	GAGAGTGGATGGATG[-/AATGGGTA]GGTGGATGGGTAAAT	84900
rs199988962	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116794669	GAAGGAAGGGAGGAA[-/G]GGAAGGGAGGGAGGG	84900
rs199994553	snp	C/T	0.000340483	0.0130432	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849477	GGACACCCAGAAGGA[C/T]GCCAAGGGTCAGCAT	84900
rs200148806	snp	C/G	0.00194142	0.0310957	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737930	GGGGCGCGGCGGCCG[C/G]GGCGCGGAACGCGGC	84900
rs200161684	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852597	AAAAACCAAAGGGAA[A/G]CAACAGGAACTTCTG	84900
rs200221377	in-del	-/A	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116780910	GTTCAGATCCCAGCC[-/A]TACGCCTCTCCAGCT	84900
rs200242720	in-del	-/GGATGGATGGAT			intron-variant	RNFT2	GRCh38.p7	12:116788956	TAAATGGGAGGAGAG[-/GGATGGATGGAT]GGATGGATGGATGGA	84900
rs200244608	snp	A/C	0.492871	0.0592773	intron-variant	RNFT2	GRCh38.p7	12:116749288	CCTCTTTCCCCCCCC[A/C]CCACCCCTTTTGAGA	84900
rs200259830	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116797553	AAAAAAAAAAAAAAA[-/A]GTTATTAAGTTAGAG	84900
rs200260347	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805121	GGGTTAAGACATTGT[C/T]TTTTTTTTTTTTTTT	84900
rs200325455	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116803740	AGGACAATTTCTCAA[C/T]TTGAGGTGTATATAA	84900
rs200331112	snp	C/T	0.00103928	0.0227719	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750277	TTCATCCTGATCCTC[C/T]TGGCCAAACTGTGCT	84900
rs200341108	in-del	-/T	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116753072	GTCTGTTAGCTGGGA[-/T]TTTTTTTTTCTCATT	84900
rs200360671	in-del	-/CC			intron-variant	RNFT2	GRCh38.p7	12:116749280	AATCTCTTCCTCTTT[-/CC]CCCCCCACCACCCCT	84900
rs200438634	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813453	TCTGGCTGACCCCTC[A/G]TCACCCCATCACCCT	84900
rs200443875	snp	A/C/T			intron-variant	RNFT2	GRCh38.p7	12:116826305	AACTTGACACTCCCA[A/C/T]CCCCTTTATCTGAAT	84900
rs200527065	in-del	-/TAGAG	0.0352966	0.128072	intron-variant	RNFT2	GRCh38.p7	12:116831645	CAGACATAGAATTGT[-/TAGAG]TAAAGATTATACATA	84900
rs200564095	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841778	ATAAATATATATATA[A/T]AAATATATATATATA	84900
rs200616633	in-del	-/T	0.144296	0.226554	intron-variant	RNFT2	GRCh38.p7	12:116807856	TCACCCAAACCGGTG[-/T]GCTTTGATGCGATTG	84900
rs200706559	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116746106	GCCAAGCATAGTGGC[A/G]CACACCTGTAATCCC	84900
rs200711260	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116772103	TCTCAGATTTTTTTT[A/T]ATTTTGGAGACACAG	84900
rs200725673	snp	A/C/T	0.00463238	0.0479062	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836299	TGAGCAGGGCTCAGG[A/C/T]GGGACCATTGGAGAC	84900
rs200741708	snp	A/G	0.00119392	0.0244035	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750145	TCCCTGCTGCAGCAC[A/G]TGGGTGGGGACCACC	84900
rs200752325	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116850638	TTTTTTTTTTTTTTT[G/T]TTGTTGTGAGACAGA	84900
rs200800488	in-del	-/CTGT	0.0414363	0.137845	intron-variant	RNFT2	GRCh38.p7	12:116797528	CCACTGCACTCCAGC[-/CTGT]CTATCTCAAAAAAAA	84900
rs200814106	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116788959	ATGGGAGGAGAGGGA[G/T]GGATGGATGGATGGA	84900
rs200815684	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116832150	AAAAAAAAAAAAAAA[A/T]ATATATATATATATA	84900
rs200853523	in-del	-/GATG	0.0759472	0.179459	intron-variant	RNFT2	GRCh38.p7	12:116789440	GGTGGATGGATGGTA[-/GATG]GATGGATGGATGGAT	84900
rs200858485	snp	G/T	0.0850919	0.187897	intron-variant	RNFT2	GRCh38.p7	12:116801808	TGTGGGGTTTTTTTT[G/T]TTTGTTTGTTTGTTT	84900
rs200862754	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824906	TAGCACCAGCTGAGT[A/G]GCCTTAGATGGTACT	84900
rs200907895	in-del	-/ATATAGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116845271	AAAATATATATATAT[-/ATATAGAGAG]AGAGAGAGAGAGAGA	84900
rs200927040	snp	C/G	2.16368e-05	0.00328906	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737764	AGGAAGAAGGGAAGG[C/G]GAGGAGGGGAAGGGC	84900
rs200961313	in-del	-/G	0.00993281	0.0697692	intron-variant	RNFT2	GRCh38.p7	12:116811445	CAGTGGGGCCATCTC[-/G]GCTCACTGCAACCTC	84900
rs200992281	in-del	-/AGAT			intron-variant	RNFT2	GRCh38.p7	12:116789235	AAATGGGAGGAGAGT[-/AGAT]GGATGGGTGGATGGG	84900
rs200994790	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116843706	CCTCAGCTGGGCCCT[G/T]GGGTAAACCTGGTTT	84900
rs200999133	snp	A/C	1.91115e-05	0.00309118	upstream-variant-2KB, missense, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737878	AGAAGCCGGCGCCAC[A/C]CCATGGCCGCCAGGT	84900
rs201001033	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116798237	CTCAAAAAAAAAAAA[-/A]GAAGCAGCAGCAGCA	84900
rs201036467	in-del	-/AAAAT			intron-variant	RNFT2	GRCh38.p7	12:116806379	TCTCAAAAAAAAAAA[-/AAAAT]ATATATATATATATA	84900
rs201046821	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116832150	AAAAAAAAAAAAAAA[-/T]ATATATATATATATA	84900
rs201156070	in-del	-/GGCTTGGCA			cds-indel, intron-variant	RNFT2	GRCh38.p7	12:116852386	CAGGACTTTCCCCTT[-/GGCTTGGCA]TCCCTGGCTCTCTCC	84900
rs201179586	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775282	AAAAAAAAAAAAAGA[C/T]AGAGAGAAGAGCAAC	84900
rs201181081	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116768928	TAGAGAAAGTGTTTT[G/T]CCATATTGGCCAGGC	84900
rs201187787	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789952	ATGGATGGATGGTGG[A/G]TGGGTGGGTGGATGG	84900
rs201191790	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754991	AGCTCTTTAGTTTAA[C/T]TAGGTCCCAGCTATT	84900
rs201216733	snp	G/T	0.0126979	0.078662	intron-variant	RNFT2	GRCh38.p7	12:116774223	GTGGTTGGATAGTGG[G/T]GATGATTATGCAACA	84900
rs201247739	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116829974	GGATTTTTTTTTTTT[-/T]GCATTCTCTATTATT	84900
rs201250431	snp	C/T	1.64969e-05	0.00287196	intron-variant	RNFT2	GRCh38.p7	12:116835922	GGTCACGAGTGATCC[C/T]TGGGTACATTTCAGC	84900
rs201256496	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782093	CCAAAAAAAAAAAAA[A/G]ATGTGGACATCATGC	84900
rs201262887	snp	A/G			utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852377	CCACCAAACCAGGAC[A/G]TTCCCCTTGGCTTGG	84900
rs201263220	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116788907	AAATGGGAGGAGAGT[-/G]GATGGATGGATGGTG	84900
rs201303361	snp	G/T	0.0314385	0.121371	intron-variant	RNFT2	GRCh38.p7	12:116850629	TCTTTTCTTTTTTTT[G/T]TTTTTTTTGTTGTTG	84900
rs201317508	in-del	-/A	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116818153	AGACCCCCTCTCTAC[-/A]AAAAAAAGTCTTTAA	84900
rs201319926	in-del	-/TTTTTTG			intron-variant	RNFT2	GRCh38.p7	12:116756309	ATATTCCTAAGGTTT[-/TTTTTTG]TTTTTTGTTTTTTGT	84900
rs201488125	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116851230	ACATCTAAAAAAAAA[-/T]AAATTTATTAGAGAT	84900
rs201494908	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116795411	AGAAAAAAAAAAAAA[-/A]GAAAGAAGAAAGAAA	84900
rs201551601	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116820484	CTGGATTGGCTGTGG[G/T]GGATATGGAACATTT	84900
rs201587218	in-del	-/AA	0.10237	0.201756	intron-variant	RNFT2	GRCh38.p7	12:116797644	TTGGCTTTGCCCAAG[-/AA]AGAATTCAAGGGTGA	84900
rs201613636	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853074	AACGTCCCATCTGAG[G/T]TTTTCTTCTCGGTGG	84900
rs201616544	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116832146	AAAAAAAAAAAAAAA[A/T]AAATATATATATATA	84900
rs201622019	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116786269	TGGGATTATAGACAC[A/G]TGCCACCACGCCTGG	84900
rs201661781	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804865	CCAGCTATTCAGGAA[A/G]CCGAAGTGGGAGGAT	84900
rs201722595	snp	A/G/T	0.00166291	0.0287873	synonymous-codon, missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779210	CCTCATATTCCTGAA[A/G/T]CCCAACCTGGAGATG	84900
rs201724216	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116832898	TACCCAAGTCGTGTT[C/T]TTTTTTTTTTTTTTT	84900
rs201734984	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116822363	CTCTCTCTCTCTCTG[A/C]GGCAATTCCAGCTGT	84900
rs201754796	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116769876	GTCTCTACTAAAAAA[A/G]ATACCAAAATTAGCC	84900
rs201768000	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813546	TGCTTCCATAGCCCC[A/G]AGGCCACTTCTGTTG	84900
rs201801655	snp	A/G	0.00023065	0.0107365	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835981	GACATCTGTGGACGT[A/G]TGGGCGGAGTTAGGA	84900
rs201814580	in-del	-/TC			intron-variant	RNFT2	GRCh38.p7	12:116753152	TTTTCTTTTTCTTTT[-/TC]TTTTTTTTTTTTTTT	84900
rs201827707	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116797875	AAGGGGTAGTCACTT[C/T]TGGGTCACTGGGTGA	84900
rs201889434	snp	C/G/T	0.115088	0.210473	intron-variant	RNFT2	GRCh38.p7	12:116850632	TTTCTTTTTTTTTTT[C/G/T]TTTTTGTTGTTGTGA	84900
rs201896202	snp	A/C	0.000123293	0.00785055	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737823	GAGGAAGTAGACGAG[A/C]GACAGCCCGAAGACC	84900
rs201902456	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116801832	TTTGTTTGTTTGTTT[G/T]TTTTTTTGAGACAGA	84900
rs201927819	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116772104	CTCAGATTTTTTTTT[A/T]TTTTGGAGACACAGT	84900
rs201955977	in-del	-/AAAAAATAT			intron-variant	RNFT2	GRCh38.p7	12:116806377	TGTCTCAAAAAAAAA[-/AAAAAATAT]ATATATATATATATA	84900
rs202035087	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116825101	ATGCGTCAGCTGCAA[C/T]GGCAGGAATGGCCTT	84900
rs202072712	snp	C/G	0.000883302	0.0209969	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749871	GCTCAGCTCCGAGGC[C/G]AGTGTGGATGAAGGT	84900
rs202074743	in-del	-/AGAGAGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116845275	TATATATATATATAT[-/AGAGAGAGAG]AGAGAGAGAGAGCTC	84900
rs202079221	in-del	-/GTA			intron-variant	RNFT2	GRCh38.p7	12:116789970	GTGGGTGGATGGATG[-/GTA]GATGGATGGATGGAT	84900
rs202109683	snp	A/C/G			intron-variant	RNFT2	GRCh38.p7	12:116755001	TTTAATTAGGTCCCA[A/C/G]CTATTTATCTTTGTT	84900
rs202136948	in-del	-/AAAATAT			intron-variant	RNFT2	GRCh38.p7	12:116806379	TCTCAAAAAAAAAAA[-/AAAATAT]ATATATATATATATA	84900
rs202173486	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116803095	GCAAGACCCTGTCTT[A/T]AAAAAAAAAATCAAA	84900
rs202194187	in-del	-/TTCA	0.277733	0.248457	intron-variant	RNFT2	GRCh38.p7	12:116809188	TTAGAGCTGAGTTTG[-/TTCA]TTCATTCATTCATTC	84900
rs202238131	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791403	GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC	84900
rs367547840	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753551	GCATCATTCACTAAC[C/T]GCTAGGGATTATGAT	84900
rs367592439	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116813025	CAGTGGCACGATCAC[C/G]ATTCATTGCAGCCAT	84900
rs367598188	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116795125	TTTATGAAAATGAAG[G/T]CCGGGCCCGGTGGCT	84900
rs367615379	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780424	ACGGTTCCCACTCCT[A/G]GGAGAATCTACTGCC	84900
rs367645340	snp	C/T	9.24172e-05	0.00679706	missense, intron-variant	RNFT2	GRCh38.p7	12:116849381	GCCCGCTCTGCCGCT[C/T]GGTCGCCGTGGACAC	84900
rs367648587	snp	A/G	2.08327e-05	0.00322737	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750239	TGAAGGCTGTGATCT[A/G]CTGGCTCCAGAAAGG	84900
rs367827348	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768346	CCTCAGGTGATCCGC[C/T]GGCCTTGGCCTCCCA	84900
rs367845818	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116771492	AAAAAAAAAAAAAAA[A/T]AAATACGTATATGAG	84900
rs367865575	snp	C/T	2.58101e-05	0.00359227	intron-variant	RNFT2	GRCh38.p7	12:116740988	TGGCAATCTGACAGG[C/T]AGTGGGAGTGTTGGG	84900
rs367867485	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116785877	AGCATGGTGAAACCC[C/T]GTCTCTACAAAAAAT	84900
rs367883763	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833433	GGATGCGGAGGGCAG[A/G]GACTGTGCCCCCACC	84900
rs367888385	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116804960	TGATGAAGTGAAACC[C/T]TGTCAAAAAAGAAAA	84900
rs367899205	in-del	-/GTTA			intron-variant	RNFT2	GRCh38.p7	12:116801613	AGTGCTGGCTGGTTA[-/GTTA]ATTATTGTCATTCTG	84900
rs367983429	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116746374	CCAAGTGATTATAAT[A/G]TATGGCCAGGATTGA	84900
rs367993280	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116780267	TTTTGGCACCAGGAA[C/T]CGGTTTCATGGAAGA	84900
rs368005148	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116762562	GGCAACATAGCAAGA[C/T]CCCTTTCTTCTCTAC	84900
rs368057295	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752945	ACAAAAAGCAGGACT[C/T]GAAAATCATTATTTG	84900
rs368061393	snp	A/G	0.000153988	0.00877328	intron-variant	RNFT2	GRCh38.p7	12:116836034	CTCTCAGGTGAGTTG[A/G]CTTCAGGTGGTCCCC	84900
rs368062736	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794867	TGATGTTATTCAGGA[C/T]CTGTTTGCTTACAGG	84900
rs368078163	in-del	-/TT			intron-variant	RNFT2	GRCh38.p7	12:116846902	CTAGCATGCCCAGGA[-/TT]TTTTTTTTTTTTTTT	84900
rs368090730	in-del	-/AGGG			intron-variant	RNFT2	GRCh38.p7	12:116839794	GGGAGGGAGGGAGGG[-/AGGG]GCGGAGGGGCCCACT	84900
rs368225477	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749240	CCTGGGTCTTTACAT[C/G]GTCTACTCTCTGTAC	84900
rs368226731	in-del	-/GAG			intron-variant	RNFT2	GRCh38.p7	12:116775280	AAAAAAAAAAAAAAA[-/GAG]AGAGAGAAGAGCAAC	84900
rs368232252	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789706	TGGATGGGTGGATGG[A/G]TAAATGGGAGAAGAG	84900
rs368234341	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801756	TCTGGGCCCTTAGGG[A/G]GATGTTAATAGGCAT	84900
rs368240174	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116776051	CTCAAAAAAAAAACA[A/T]AAAAACTCGTAATTA	84900
rs368272123	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116775619	CAAAATTGGAACCAA[C/G]TCCACATTCTTCCCT	84900
rs368315311	snp	A/G	0.000329946	0.0128399	intron-variant	RNFT2	GRCh38.p7	12:116740529	TGAATCAGGTGACAC[A/G]TCTCCAAGAGAATTT	84900
rs368356015	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763776	AGAGCGAGACTCCAT[C/T]TCAAAAAAAAAAGGG	84900
rs368376444	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116746028	GATCACTTGAGCTCC[A/G]GAGTTCGAGACCAGC	84900
rs368390146	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116813438	GTCTCCCCAGCCCCA[C/T]CTGGCTGACCCCTCA	84900
rs368400939	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835178	TTTTACAGGTTAAGA[A/G]ACTGAGGTTCAGGGA	84900
rs368410299	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116744518	GAAGGAAATTACCTA[-/AA]GTCACACAGCCAGGA	84900
rs368451296	snp	A/G	0.000181239	0.00951769	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754036	CTATGCCAACTCCAC[A/G]CTTCGAGAACAGGTC	84900
rs368488607	snp	G/T	3.25781e-05	0.00403584	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750182	ACTCGGAGGAGGGAG[G/T]CGACGAGCAGCCTGG	84900
rs368489533	snp	A/G	6.59044e-05	0.00574002	missense, intron-variant	RNFT2	GRCh38.p7	12:116849402	CCGTGGACACCCTGC[A/G]CTGCTGGAAGGACGG	84900
rs368490362	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116788982	TGGATGGATGGATGG[A/G]TGGGTAGATAAATGA	84900
rs368494729	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116769138	GCCAAGGTGGGCAGA[C/T]CACGAGGTCAGGAGT	84900
rs368495506	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116825008	CAGTCAGGACACACC[A/G]GGTACAGCTTGTCTC	84900
rs368502100	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116832933	TTTTTGAGATGGAGT[C/T]TTGCTCTGTTGCCCA	84900
rs368502255	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811134	CATGATGGCTCACGC[C/T]ACTCGGAAGTTTGTC	84900
rs368507717	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768707	TTTACTATACTTTTC[A/G]TTGTCATTTTTTTTT	84900
rs368519851	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116740183	CTTAAAAAAAAAAAA[-/A]GGAGTTTCAAGGGGG	84900
rs368544434	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797211	TGCCCCCCAAAATAT[A/G]TGTGTTGGAGTCCAA	84900
rs368548679	in-del	-/TGGA			intron-variant	RNFT2	GRCh38.p7	12:116839426	GGATGGGTGGGTGGG[-/TGGA]TGGATGGATGGATGG	84900
rs368596004	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116787620	AATTGAGAGGCTGAA[C/G]TGGGAGGATCATTGA	84900
rs368634120	snp	A/G			missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754001	ATTGCTGTGTGCATC[A/G]GGATGGCCAGCACCT	84900
rs368676047	snp	C/T			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853061	TACCCTCTGGGGGAA[C/T]GTCCCATCTGAGGTT	84900
rs368723554	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849545	GGCCTCAAGCACTTA[C/T]ATCCTGCCTCTTGCC	84900
rs368772415	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116826187	CCTTCATTTCCCACC[C/T]GCTTCTGGAGCCAGC	84900
rs368775467	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116847927	GTGCCATGGTGGTTT[C/G]CTGCACCTATCAACC	84900
rs368800571	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116797483	AGACTCACTTGAACC[C/T]GGGAGGTGGAGGTTG	84900
rs368800835	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829132	GAGACATGAGGGAGG[C/T]ATGGGGCAGCTGAGG	84900
rs368827046	snp	C/T	5.14284e-05	0.00507066	intron-variant	RNFT2	GRCh38.p7	12:116741102	CCTGAAAGGTAGGCA[C/T]CCCTGCTTCTGTTCC	84900
rs368845183	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116827944	GCTGTGCTCTTGACC[A/G]CCAAGCCAGACTGGT	84900
rs368897674	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837002	TAAAGTAGATCATCC[A/G]TGGAAAGAACTAAAT	84900
rs368906849	in-del	-/CAA			intron-variant	RNFT2	GRCh38.p7	12:116816839	AAAAACAAAAAATAA[-/CAA]ATACTCGTGTACCCA	84900
rs368915136	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116747161	TCCTGGGCTCAAGCC[A/G]TCCTCCCACCTCAGC	84900
rs368933651	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116848995	GGCTAATTTTTGTAT[G/T]TTTTAGTAGAGACTG	84900
rs368983165	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116750862	ATATAATATATATTA[C/T]ATATATATAATATAT	84900
rs368997333	snp	A/G	0.000153988	0.00877327	intron-variant	RNFT2	GRCh38.p7	12:116741022	CTCTGGCTCACCCAT[A/G]TGTTGGGTTTTAGGT	84900
rs369018864	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775822	CCAAGGTGGGTGGAT[C/T]ACTTGAGGCCAGGAG	84900
rs369021183	snp	A/G	1.65111e-05	0.0028732	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833813	TTCTATCTGGTCATC[A/G]AGGAGCTGAGCCAGC	84900
rs369022525	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116792328	GTGCTGGGATTACAG[G/T]TATGAGCCACTGCGC	84900
rs369022617	in-del	-/CT			intron-variant	RNFT2	GRCh38.p7	12:116778886	CCACCTCTTTCCTCT[-/CT]ATAAGTTACCCAGCC	84900
rs369077863	snp	A/T	0.000180799	0.00950615	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836313	GCGGGACCATTGGAG[A/T]CCAAGGCTGGGGGAG	84900
rs369086225	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772390	CGGCTCACTGCAACC[C/T]CCAGCTCCCTGGTTC	84900
rs369097268	in-del	-/GCCTCTCTCT			intron-variant	RNFT2	GRCh38.p7	12:116786961	ATGATGCCTCTCTCT[-/GCCTCTCTCT]TATAAGGACACATGT	84900
rs369110791	snp	A/G	3.99768e-05	0.00447066	synonymous-codon, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836210	AGCCACCGGGCAGCA[A/G]TGCACAGAAGCTGGT	84900
rs369114069	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116829644	TCTCTGTCCACATGC[C/G]ACGCATACGATGTAA	84900
rs369134503	snp	A/G	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116769197	ACCCCTGTCTCTACT[A/G]AAAATACAAAAATTA	84900
rs369173206	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116811394	TTTTTTCCTTTTTTT[G/T]AGACAGAGTCTCACT	84900
rs369198479	in-del	-/AGAT			intron-variant	RNFT2	GRCh38.p7	12:116789440	GGGTGGATGGATGGT[-/AGAT]GGATGGATGGATGGA	84900
rs369200614	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796517	TTGGTTTTTCTCTAA[A/G]CACAGGGACGGGGAG	84900
rs369281917	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116848458	CCTACCATGGGCCCC[C/T]TACTTCTCTCAGAAT	84900
rs369296730	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116813988	TTTTGATCACTACAG[C/T]TTAGTAAGTGCTAGG	84900
rs369306386	in-del	-/ATGG			intron-variant	RNFT2	GRCh38.p7	12:116789441	TGGATGGATGGATGG[-/ATGG]GTGGATGGGTAAATG	84900
rs369315267	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765385	AGATGCATTTGTTTC[A/G]TCCACTCTCTGGAAA	84900
rs369325063	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836465	GGGTGGACTTGGGCA[C/G]GTTATTTCACCTCTC	84900
rs369446293	in-del	-/AC			intron-variant	RNFT2	GRCh38.p7	12:116749288	CCTCTTTCCCCCCCC[-/AC]CACCCCTTTTGAGAC	84900
rs369457621	snp	C/T	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116759785	GGGTGCAATGGACTC[C/T]GTGAGGGTTCTTAGC	84900
rs369460415	in-del	-/TAACTTTTG	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116796073	ACCACCACACCCAGC[-/TAACTTTTG]TATTTTTAGTAGAGA	84900
rs369498211	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116784339	CCAGTTCAGCTCTTG[C/G]GAGAAGGTCTGATTG	84900
rs369518779	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116828849	GGGAAGAGTGACAAA[-/A]GCAGGTTAAGGCCAG	84900
rs369542259	in-del	-/AT			intron-variant	RNFT2	GRCh38.p7	12:116750830	TATATTATATATATA[-/AT]ATATATATTATATAT	84900
rs369545531	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116818434	TTCAGCACTGCCGTT[C/G]AGTAAATGTCATGTC	84900
rs369551429	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794648	GGGAGGGGAGGGGAG[A/G]AGGAAGGAAGGAAGG	84900
rs369552376	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116801165	GCAGTGAGCAGCAAA[G/T]CCAGGGGGTGCTGAG	84900
rs369583636	in-del	-/TAT			intron-variant	RNFT2	GRCh38.p7	12:116750907	ATATATATATATATA[-/TAT]TTTTTTTTGAGACAG	84900
rs369665946	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781470	ATTTATTATCTTATC[A/G]TTCTGGAGGTTAGGA	84900
rs369678850	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765126	GTAAGCTTAGGCGTC[A/G]CAGCTGATTAGGAGA	84900
rs369720938	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116750851	ATATTATATATATAT[-/AA]TATATATTATATATA	84900
rs369732619	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116772976	TAGGACTACAGACAC[A/G]TGCCACCACATCCAG	84900
rs369734304	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779234	GGAGATGCTGGACTT[C/G]TTTGACCTGCTATGG	84900
rs369739801	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116780776	CAAGACCATGAATGA[C/T]GAGGACCTTTTGCCC	84900
rs369741261	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760971	GTAGCCTCCAACTCC[C/T]GGATTCAAGCAATCC	84900
rs369743645	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739034	GGCTTCACTGGCGGG[C/T]CATTTTTAATCAGTG	84900
rs369749000	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795554	TGAGTTCCTCAGTTG[C/T]ACCAACCACGTTTCA	84900
rs369772256	in-del	-/T	0.10237	0.201756	intron-variant	RNFT2	GRCh38.p7	12:116850795	ACCATGCCCAGCTAA[-/T]TTTTTTTTTGTATTT	84900
rs369789927	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116774935	AACTGGTGCACAGAA[-/AG]AGAGAGAGAGAGAGA	84900
rs369802544	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841894	ATAAATATATATAAA[A/T]ATATATATATATAAA	84900
rs369831352	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116785891	TGTCTCTACAAAAAA[-/A]TACAAAAAAAAATTG	84900
rs369848980	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786324	CCATATTGGCCAGGC[C/T]GGTCTCGAACTCCTG	84900
rs369883723	snp	C/T	9.44956e-05	0.00687305	intron-variant	RNFT2	GRCh38.p7	12:116836144	CGTAGTTCCCAAGGG[C/T]GCCCATAGCTGTATT	84900
rs369902412	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116747137	TCTTAACTCACTGCA[A/T]CCTCCACCTCCTGGG	84900
rs369908747	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116843269	AGGCTGAGGCGATTG[A/G]ATCCCTTGAGCCCAG	84900
rs369913393	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116788708	GAAGTGTTCATTGTA[G/T]GTATGTAAGTATGTA	84900
rs369916906	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116832666	CTCCATTTTACAACA[C/T]AGGCCACAGAAAGCT	84900
rs369937790	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116756132	TTGATGAGGATTGCA[C/T]TGAATTTGTAGATTG	84900
rs369942537	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852472	GCTCCGTTACTATGG[C/T]GATGGCCATGATGTT	84900
rs369994267	snp	A/C			stop-gained, intron-variant	RNFT2	GRCh38.p7	12:116849340	TGAGGAGTGCCTCTG[A/C]CTGTGGCTGGACCGT	84900
rs369994475	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116829017	TGGAAAAAAAAAAAA[-/A]CTGCAGGTCAAGACT	84900
rs370095125	in-del	-/GTCT			intron-variant	RNFT2	GRCh38.p7	12:116797530	ACTGCACTCCAGCCT[-/GTCT]ATCTCAAAAAAAAAA	84900
rs370109872	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805577	CCTCCCGGGTTCCAG[C/T]AAGTCTCGTGCCTCA	84900
rs370115729	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116776723	CTATGCTGAGTGTAC[C/T]TCTCCCTGCTTTGGA	84900
rs370119629	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116742681	CATGCAGTGACTCAC[A/G]CCTGTAATCCCAACA	84900
rs370134028	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808894	GTTGGAAATCGACCT[C/T]CAGGTTGAAAGATGA	84900
rs370168756	snp	A/C	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116786048	TAGAGCCAGCCTCTC[A/C]GTATTCTTCTGACAT	84900
rs370173024	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771406	TCAAGGCTGCAGTGA[A/G]CCATAATCACACCAC	84900
rs370183249	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116754210	ACATATCAGTGAGAA[C/T]GTACAATGTTTGGTT	84900
rs370190754	in-del	-/GTTGGCCAGGCTGGCC			intron-variant	RNFT2	GRCh38.p7	12:116850835	ATGGGGTTTCACCAC[-/GTTGGCCAGGCTGGCC]TCAAACTCCTGACCT	84900
rs370192277	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116801129	TGAGGAAACTGAGGG[C/T]CAGCAAGGGAATGCC	84900
rs370224894	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116804241	TGTGTATTCTTGCTT[C/G]TCAAAGTGCAGTCCC	84900
rs370232515	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116790813	ATACAAAGATTTAGC[C/T]GAGCATGGTGGCACT	84900
rs370265880	in-del	-/GAG	0.44252	0.159487	intron-variant	RNFT2	GRCh38.p7	12:116841966	ATATATATAGAGAGA[-/GAG]AGAGAGAGAGAGAGA	84900
rs370347412	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765855	GGCAGCGGGCCAGAG[A/G]TCTTCCCTAGAAAAA	84900
rs370361656	snp	G/T	0.00196122	0.0312532	intron-variant	RNFT2	GRCh38.p7	12:116753961	TCTAAGTGGGTGACA[G/T]CAGGCCCTTCTCTGT	84900
rs370363231	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833947	CCTCTGCAAGGTGAG[A/G]TGGCCCCAAGGCTGG	84900
rs370369031	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116758283	CTATTCTGTGATTCT[A/G]TGTCTTTTAAGTGGA	84900
rs370379723	snp	A/T			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836592	CCCTGTGGGTCAGTC[A/T]CTCTCTCTCTGAGCC	84900
rs370420491	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116850610	TGTGAAGTATTTTTT[A/C]TTTTCTTTTCTTTTT	84900
rs370425047	snp	A/C	1.6498e-05	0.00287206	intron-variant	RNFT2	GRCh38.p7	12:116836052	TCAGGTGGTCCCCAC[A/C]AGGGTCCTGAGAATC	84900
rs370436434	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116771175	GACGTTAAACATGTG[C/G]ATAGTCCAGGTGCGT	84900
rs370440873	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116777208	CAGTCGTGAGCCACC[A/G]TGCCCAGCCTCAAAA	84900
rs370456599	in-del	-/GGACATAATAAT			intron-variant	RNFT2	GRCh38.p7	12:116836944	CAAAGAAAAAAAAAA[-/GGACATAATAAT]AACAGCTACTTCATA	84900
rs370500377	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809927	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	84900
rs370512415	snp	A/G	0.000157988	0.00888644	upstream-variant-2KB, utr-variant-5-prime, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737920	GCGCGGACGTGGGGC[A/G]CGGCGGCCGGGGCGC	84900
rs370514912	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116753148	TTCTTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	84900
rs370520324	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116812526	TCTGTGTCTAGGCCT[C/G]TTCCTATCTTTTTTT	84900
rs370562862	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760180	TGCAAAACGAAGGGC[C/T]GGTCTCACTCCCACC	84900
rs370570848	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815664	TCCCCATCTCAGGAG[C/T]CTTAATTTCATCACA	84900
rs370576680	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116789602	TAGGAGAGTGGTGGG[C/T]GGATGGATGGTAGAT	84900
rs370589867	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853279	TTAATCGAGTATCAG[A/G]TTCACAGTATCCTGC	84900
rs370612079	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116787108	AGCTTCCTGGTATCC[C/T]TGAGTGGCCGTTATT	84900
rs370637465	snp	C/T	0.000169986	0.00921759	intron-variant	RNFT2	GRCh38.p7	12:116849309	GCTGATTGCTGTCCC[C/T]GCAGCACGTGTTCTG	84900
rs370708267	snp	C/G	0.000125392	0.00791708	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749902	GGCGTCTTTGAGAGT[C/G]TGAAGGCAGAGGCAG	84900
rs370793163	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849841	CTCCTTCCTTCCTTC[C/T]TTCCTTTTTTTTTTT	84900
rs370793327	snp	A/G	0.000115332	0.00759293	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835975	TCCTTCGACATCTGT[A/G]GACGTGTGGGCGGAG	84900
rs370819208	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116749260	ACTCTCTGTACCTGT[G/T]TCCTAATCTCTTCCT	84900
rs370851596	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853198	GCCAGGAGTCCCCGT[C/T]GGAAAAGAACAATGC	84900
rs370865454	snp	C/T			synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766885	CCTCTATGTGCTTTA[C/T]ACATTCAGCTCCCAG	84900
rs370870549	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116771488	AAAAAAAAAAAAAAA[A/T]AAAAAAATACGTATA	84900
rs370871551	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739633	AAGTATTCCAAGGGG[A/G]GGGCACAGCAAGTGC	84900
rs370907212	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809278	TCCATCAGAGGTTGC[A/G]TTTGAACTCGATTCC	84900
rs370953172	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116785276	GTGTGTGTGTGTGTG[G/T]CGGGGGGGGGTTGTT	84900
rs370982600	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750904	ATAATATATATATAT[A/T]TATATTTTTTTTTGA	84900
rs370990888	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116796427	CATCTTAACTAAGTT[C/G]TAGCTCAGTAGGCTC	84900
rs371010925	snp	A/G	0.000246139	0.0110909	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740475	CCTACCTCCAGTGTC[A/G]TCAACATGGAGTTCT	84900
rs371136755	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820112	TTTGTTTGTTTTTAA[A/G]GACAGTCTTACTGTG	84900
rs371158023	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116794523	GGATTGCTTGAACCC[A/G]GGAGGGGGAGGCTGC	84900
rs371166283	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116761089	GCAGCATCTCCTCCA[C/G/T]GTACACCTAGCCCAG	84900
rs371167096	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763651	GGATGTGGTGGCAGA[C/T]GCCTGTAGTCCCAGC	84900
rs371267022	snp	G/T	0.000181983	0.00953722	intron-variant	RNFT2	GRCh38.p7	12:116849280	CAGACGCTCAGTAAA[G/T]AGTCCTGGTGCCTGC	84900
rs371307819	in-del	-/TGCCTCTCTC	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116786950	CTCTTCTGTGAATGA[-/TGCCTCTCTC]TGCCTCTCTCTTATA	84900
rs371348401	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116822799	CTGAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT	84900
rs371362710	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116816581	GTTATCTAGTGGCAG[A/T]TGTTGTGGGTAAGAG	84900
rs371364134	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116849257	TTCTCCTGCTCCCGA[C/G]ACCGAGGCAGACGCT	84900
rs371373719	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116775261	GTGAAACTCCCGTCT[A/C]AAAAAAAAAAAAAAA	84900
rs371379791	snp	C/T	6.59196e-05	0.00574068	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116753997	AGGCATTGCTGTGTG[C/T]ATCGGGATGGCCAGC	84900
rs371456627	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116764023	TTCTACTCAGCCATA[A/T]AAAGGAATGAATTAA	84900
rs371473732	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116807899	GCCTCAAACTCCTGG[A/G]CTCAAACGATCCTCC	84900
rs371479059	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829438	CAGGAGGGGAAAGGA[A/G]GGCCCTTTGGGAAAC	84900
rs371479863	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787958	TTGAGATGGAGTGTC[A/G]CTCTTGTTGCCCAGG	84900
rs371480237	snp	A/C/G	0.000957517	0.0218615	intron-variant	RNFT2	GRCh38.p7	12:116766940	GAATCCAACCCCCAC[A/C/G]GTGGGAGAGTGGGGC	84900
rs371486786	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116794996	AACTTAGCCCAAACC[A/T]TGGTAAGAAGGCAAA	84900
rs371486905	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116821454	GACTCTGCCAGCTGT[C/G]GTCCCCACAACCCCA	84900
rs371490717	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772181	ACTGCAGCCTTGAAC[C/T]TCTGGGCTCAAGCGA	84900
rs371551672	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116846490	GGAGGAAGTCTCGCC[A/G]TGTTGCCCAGGCTGG	84900
rs371575320	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778799	AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC	84900
rs371581618	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116780270	TGGCACCAGGAACCG[G/T]TTTCATGGAAGACAG	84900
rs371622582	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116836804	GCATGGTGGCACACA[C/G]CTCTAGTCCCAGCTA	84900
rs371674780	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758700	GCCCCAATCCCTTCT[A/G]GCTTGTAGGGTTTCT	84900
rs371693356	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116742055	AGATTTTTATTTCTT[A/C]CATTTCTCAAGATGA	84900
rs371710601	snp	A/G	4.94319e-05	0.00497127	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754041	CCAACTCCACGCTTC[A/G]AGAACAGGTCTCACT	84900
rs371712573	in-del	-/TGGG			intron-variant	RNFT2	GRCh38.p7	12:116788983	GGATGGATGGATGGA[-/TGGG]TAGATAAATGAGAGG	84900
rs371726681	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116805056	AAGCTTTTCGCATTA[C/G]TTTGAAATCCCTTAT	84900
rs371736193	snp	C/G	0.000155988	0.00883005	intron-variant	RNFT2	GRCh38.p7	12:116741009	GAGTGTTGGGAGACT[C/G]TGGCTCACCCATGTG	84900
rs371786714	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116785903	AAAATACAAAAAAAA[-/A]TTGGCCTGATGTGGT	84900
rs371835904	snp	A/G	3.21105e-05	0.00400677	intron-variant	RNFT2	GRCh38.p7	12:116836145	GTAGTTCCCAAGGGC[A/G]CCCATAGCTGTATTT	84900
rs371911298	in-del	-/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116829292	TCATGCCCTTGTCCA[-/T]GTAAAACAAACATGA	84900
rs371928335	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754270	AATAGTTTCCAATCT[C/T]ATCCAGGTCACTGCA	84900
rs371930702	snp	A/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116763630	ATAACAAAAAAAAAA[A/T]TAGCTGGATGTGGTG	84900
rs371995073	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116788984	GATGGATGGATGGAT[A/G]GGTAGATAAATGAGA	84900
rs372050554	snp	A/G	3.17153e-05	0.00398204	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750184	TCGGAGGAGGGAGGC[A/G]ACGAGCAGCCTGGGA	84900
rs372110369	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116741188	ATACCTCACCCTCAG[C/T]GTTAGTTGTTAGAGT	84900
rs372124416	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116746244	CTGCTCAAAAAAAAA[-/A]CAAGAATCACTGAGG	84900
rs372135550	in-del	-/CCG			intron-variant	RNFT2	GRCh38.p7	12:116743245	AAAAAAAAAAAAAAA[-/CCG]GTTAAAAAACACTCA	84900
rs372156237	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116804829	AAAATTAGCCAGGCA[C/T]GGTGGTACATGCCTG	84900
rs372165868	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116801799	TTTGTTTTCTGTGGG[G/T]TTTTTTTTGTTTGTT	84900
rs372165950	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789717	ATGGATAAATGGGAG[A/G]AGAGTAGATGGATGG	84900
rs372188512	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116850267	CCAAGCCATCCTCCC[A/G]CCTCAGCCTCCCAAG	84900
rs372193811	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116811453	CCATCTCGGCTCACT[A/G]CAACCTCTGTTTCCC	84900
rs372220750	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116841675	GTCACTGGAACCTGG[A/G]AGGCAGAGGTTCCAG	84900
rs372235717	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804565	TATATTACAGTAATG[A/G]TCATCTCACTACATA	84900
rs372259920	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802820	AACAGGTGGGCCTGG[C/T]GCAGTGGCTCATGCC	84900
rs372263210	snp	A/G	0.000157987	0.00888644	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849453	AGGTGTACTAGGACC[A/G]AACACTGAGGACACC	84900
rs372313573	in-del	-/TT/TTTTCTT	0.108402	0.206034	intron-variant	RNFT2	GRCh38.p7	12:116850615	GTATTTTTTCTTTTC[-/TT/TTTTCTT]TTTTCTTTTTTTTTT	84900
rs372336840	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798366	ATCTTAGAGATTGTT[C/T]GGATAAATACATAGA	84900
rs372337762	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763727	GAACTTGCAGTGAGC[C/T]GAGATCGCGCCACTG	84900
rs372339023	snp	A/G	0.000165986	0.00910854	intron-variant	RNFT2	GRCh38.p7	12:116740553	AGAATTTGCATCTTT[A/G]TTACTACTTGATTAA	84900
rs372355178	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116824601	TTCCAGACAGTAGGA[C/T]AGAGAAAGTGGGGAA	84900
rs372366092	snp	A/G	0	0	intron-variant	RNFT2	GRCh38.p7	12:116835608	TCTGATCAACACAGT[A/G]GCTGACTGGAGTGCT	84900
rs372373686	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737584	GGAGAGGGGAAGGAA[A/G]GAGGAAGATAAGGAA	84900
rs372384400	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116755670	TGCCAACAGCATGCT[A/G]GGTAACATTGTAGAC	84900
rs372387554	snp	C/G	1.64879e-05	0.00287118	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852732	ATAGAACAGTCTGCT[C/G]GGAGTCAGACCTGGA	84900
rs372398448	snp	A/G	0.000153988	0.00877327	intron-variant	RNFT2	GRCh38.p7	12:116766774	GGAAGGTTCTGCCAC[A/G]TGCACCTTTGATATC	84900
rs372410395	snp	C/T	0.000461947	0.0151908	intron-variant	RNFT2	GRCh38.p7	12:116836058	GGTCCCCACCAGGGT[C/T]CTGAGAATCAGGAAC	84900
rs372431332	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798632	GGAGTGCAGTGGCGT[A/G]ATCTCAGCTCACTGC	84900
rs372451912	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116839417	GGATGGATGGGATGG[A/G/T]TGGGTGGGTGGATGG	84900
rs372543590	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116750859	ATATATAATATATAT[-/G]TATATATATATAATA	84900
rs372581679	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784020	AGATGTAGAAGCTAC[A/G]GCACAGCACAGAGAG	84900
rs372588701	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116750521	CTTCTCTGAGCCTCA[C/G]TTTCCTCATCTGTCT	84900
rs372592529	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116768800	CAGTGGTGTGATCTC[A/G]GCTCACTGCAACCTC	84900
rs372745411	in-del	-/CAGGACAG			intron-variant	RNFT2	GRCh38.p7	12:116815863	AAGTCACCCTCCCAG[-/CAGGACAG]ATCCACACTTGAGGA	84900
rs372796222	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116781604	CTCCCTCTCCCTCCC[C/G]CTACACCTCTGCCTT	84900
rs372810473	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116795182	AGGCCAAGACAGGTG[A/G]ATCACCTGGGGTCAG	84900
rs372811461	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116787352	CAAGTCGCTTAATGT[A/G]AGCATTTTCCTCCTG	84900
rs372813330	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116753593	ATCCCTCTATGAGGT[A/G]TAAGTAATGTTATTG	84900
rs372866437	snp	A/G	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116834712	CATTGTATTTTTGAG[A/G]TTCATCCACATTGTA	84900
rs372872497	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116847931	CATGGTGGTTTGCTG[C/T]ACCTATCAACCCATC	84900
rs372899663	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808046	CGATCTCACTACAAC[C/T]TCCGCCTCCCAGGTT	84900
rs372916624	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116742265	GTACCGAGGTGGTTT[C/T]TTTTTTTTTTTTTTT	84900
rs372970198	snp	C/T	0.000147951	0.00859962	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749939	CACCAGCGCTCTTCT[C/T]GGGCTTATCAGGCAG	84900
rs372975258	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116815615	AAGGATCCTTGTGAT[G/T]ATATTGGGCCCGTCC	84900
rs372998865	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116805121	GGTTAAGACATTGTC[-/T]TTTTTTTTTTTTTTT	84900
rs373018500	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794652	GGGGAGGGGAGAAGG[A/G]AGGAAGGAAGGGAGG	84900
rs373077323	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809287	GGTTGCGTTTGAACT[C/T]GATTCCTGGTGGTTC	84900
rs373082754	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822241	CAGGACTGACCAATC[A/G]TAGAACCCCATGACC	84900
rs373103198	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116829807	GCTGGTCTTGAACTC[C/G]TGGCCTCAAGAGATC	84900
rs373103209	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777505	TCATGGATAGGTTTA[C/G]ACTACTCAGCTGTAG	84900
rs373137842	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116831508	TAACATAATCAGACC[-/C]TCTTTTTTGTACATT	84900
rs373155380	in-del	-/AATT	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116775723	TTGGACATATATCAC[-/AATT]AATATGATTCTTTTA	84900
rs373172502	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848319	CGTATGCGTGCATGT[A/G]TCTGTTTATCGTAGC	84900
rs373209293	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116808981	GCTGCCATCAGCCCC[G/T]TTTAGGATGGCCGCC	84900
rs373261109	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845742	CCTGCCCTCCAGACC[A/G]TGATGAGAATCCAGT	84900
rs373270784	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833832	AGCTGAGCCAGCTGT[A/T]CCGATCCCTTGTCCC	84900
rs373283983	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116806609	ATTAAAAAATTAGCT[C/G]AGCACGGCGGTGCAC	84900
rs373324335	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116844277	ACCCTGTAGCCCAGG[C/G]TGGAATGTAGTGGCA	84900
rs373328195	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116799505	TTGCTGGGTGCCCAC[C/T]GCACTATCTCAGAGG	84900
rs373330776	in-del	-/TGTGTTGC			intron-variant	RNFT2	GRCh38.p7	12:116793519	GCTCATATGTGTTGC[-/TGTGTTGC]ATTTGCCTGGCCTGG	84900
rs373335253	snp	C/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116812255	CCTTATCCAGGGTGC[C/G]TGGCACATAGCAGCC	84900
rs373354466	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805596	TCTCGTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	84900
rs373438259	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116769344	GACAGAGTGAGACTC[A/C]GTCTTAAAGTTAACT	84900
rs373453800	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116784519	GGAGGCTCTTTCATC[C/T]GGGGCCTGGGTTGAA	84900
rs373496166	snp	C/T	6.62888e-05	0.00575674	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749874	CAGCTCCGAGGCGAG[C/T]GTGGATGAAGGTGGC	84900
rs373498686	in-del	-/GAAA			intron-variant	RNFT2	GRCh38.p7	12:116794717	GAGGAAAGAAAGAAA[-/GAAA]TGAATTACTCTTAGC	84900
rs373521166	in-del	-/ATTAC			intron-variant	RNFT2	GRCh38.p7	12:116750831	TATTATATATATAAT[-/ATTAC]ATATATATTATATAT	84900
rs373529961	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116830534	CTCAAGGGATCCTCC[-/C]ACCTTAGCCTCCCAA	84900
rs373530940	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116802731	GGCCTCCAGATCTGG[G/T]AGAGAATAAGTTTCT	84900
rs373549768	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116824493	AGCCTGGGAGTATGA[C/T]ACCTTCCAGCCCACT	84900
rs373574043	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116827135	TGAGGCAGGAGAATC[A/G]TTTGAATCCAGGAGG	84900
rs373613840	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739191	ACAATATTGGCTCTG[C/T]CTCCAGAGACAAGAA	84900
rs373658470	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116851601	AAAAATTAGCCGGGC[A/G]CGGTGGCGGGTGCCT	84900
rs373663559	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116760243	AGGTGGAGAGCGATA[A/G]GGGCTTGAAAACCTG	84900
rs373683977	in-del	-/AAAG			intron-variant	RNFT2	GRCh38.p7	12:116851804	AGGAAGGAAAGAAAG[-/AAAG]GTCAGCTTTGGCCCA	84900
rs373776826	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737193	CTGCAGGGACCAAGG[C/G]GGTGGGCAGGTCCCT	84900
rs373844649	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784816	AGTGCTCGCCACCAT[A/G]AGACCAAAGTAGTCT	84900
rs373867951	snp	A/C/G	9.37163e-05	0.00684466	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836322	TTGGAGACCAAGGCT[A/C/G]GGGGAGAGTAGGACC	84900
rs373872956	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116782893	TCCCCAAACCCTGCC[C/T]GCACCTTTGTAAATA	84900
rs373885060	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116851744	AGTGAGACTCTGTCT[-/A]AAAAAAAAAAGAAAG	84900
rs373915598	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116771490	AAAAAAAAAAAAAAA[A/T]AAAAATACGTATATG	84900
rs373962985	snp	A/C/T	6.59482e-05	0.00574198	intron-variant	RNFT2	GRCh38.p7	12:116754074	AGGTGAGTCACTTTC[A/C/T]GACCTAGTCTCCTGT	84900
rs374022378	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739531	ACAGGGCAATATTAC[A/G]GGGAGTCAGGAGAAT	84900
rs374043161	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116750878	ATATATATAATATAT[A/G]TATTATATATATAAT	84900
rs374056983	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116770261	CTTTCTGTTTAGATA[C/T]ACAGATACCATTGTG	84900
rs374059009	snp	C/T	0.00010313	0.00718014	missense, intron-variant	RNFT2	GRCh38.p7	12:116849359	TGGCTGGACCGTGAG[C/T]GCACCTGCCCGCTCT	84900
rs374064052	multinucleotide-polymorphism	GG/TT			intron-variant	RNFT2	GRCh38.p7	12:116767568	ATATAAAAATTATGT[GG/TT]TTTTTTTGTTTGTTT	84900
rs374092829	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116776048	ACTCTCAAAAAAAAA[-/A]CAAAAAAACTCGTAA	84900
rs374094278	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849061	CTGCCTCAGGTGATC[C/T]GCCCATCTCGGCCTC	84900
rs374118458	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116820729	GCTGGATTTAAATCC[C/T]GGCTCCACCACTGTC	84900
rs374122339	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780029	AAAGAGTGTTTGAAG[A/T]CTCCTGCTTTCCATT	84900
rs374125401	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116780914	AGATCCCAGCCATAC[A/G]CCTCTCCAGCTGTGT	84900
rs374141291	snp	C/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116762802	TTTTTAGTAGAGATG[C/G]GGTTTCACCACGTTG	84900
rs374144000	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747957	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC	84900
rs374167845	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823014	AAAGCAAAAAACGAA[A/G]AGACAAAAGGAAAAA	84900
rs374215054	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816143	CGTAGCTAACAGGGT[C/T]CCAGGCCACTATGGG	84900
rs374313939	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116748881	TGTGACTCTGGACAA[C/G]TTACTTTCTCTCTCT	84900
rs374362646	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828870	TTAAGGCCAGGCATG[A/G]TGGCTCACATCTGTA	84900
rs374388001	snp	A/C/T	8.23966e-05	0.00641813	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754000	CATTGCTGTGTGCAT[A/C/T]GGGATGGCCAGCACC	84900
rs374402526	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841896	AAATATATATAAAAA[A/T]ATATATATATAAATA	84900
rs374408722	snp	A/G/T	0.000170289	0.0092261	missense, intron-variant	RNFT2	GRCh38.p7	12:116849386	CTCTGCCGCTCGGTC[A/G/T]CCGTGGACACCCTGC	84900
rs374408966	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116834000	CATTCACTAGTCAGG[A/C]CTCAGGGGGCTCCTG	84900
rs374485873	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116847937	GGTTTGCTGCACCTA[A/T]CAACCCATCACCTAG	84900
rs374532454	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807057	GTCACACTTACCGCA[C/T]GGCAGGCTGGGGAGT	84900
rs374541211	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116846969	GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC	84900
rs374554917	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116776916	TCAGCTCAAAATGGG[A/T]TTTTTTTTTTTTTTT	84900
rs374588096	snp	G/T	6.11004e-05	0.00552689	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740503	TCTGAAGTCCATGTG[G/T]CTCTTCACAGTGAAT	84900
rs374612413	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789141	GTGGATGGGTAAATG[A/G]GAGGAGAGTGAGTAG	84900
rs374635345	in-del	-/ATA	0.471768	0.115407	intron-variant	RNFT2	GRCh38.p7	12:116750827	ATATATATTATATAT[-/ATA]ATATATATATTATAT	84900
rs374644417	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116843161	ACTGGTTTAACCCCA[A/G]TTCTGTGCTTCGGGA	84900
rs374653767	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116805568	TAACCTTCGCCTCCC[A/G]GGTTCCAGCAAGTCT	84900
rs374657676	snp	A/G	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116782066	CTTGGGCGACAGAGC[A/G]AGACTCCGTCTCCAA	84900
rs374665988	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116782266	GCTCAAACCTGTAAT[A/C]CCAGCACTTTGGGAG	84900
rs374670504	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116815792	AGCCTTCCATATCCC[C/G]TACTTTGCTAACGAG	84900
rs374692998	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740429	CCTCTCTGGGATCCA[C/T]TGGTCACATCCCCCT	84900
rs374732084	snp	C/G	9.89315e-05	0.00703249	intron-variant	RNFT2	GRCh38.p7	12:116753971	TGACATCAGGCCCTT[C/G]TCTGTCCCACAGGCA	84900
rs374757003	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774273	CATTGAACTGTGCGC[A/G]TAAAAATGGTTAAGA	84900
rs374770163	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116847563	GCAGAGTTTTGCTCT[C/T]GTTGCCCAGGCTGGA	84900
rs374778924	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116814322	TAGATAAAAAGATGC[G/T]GAAATCAGTAGGCAA	84900
rs374834316	snp	A/G	8.84979e-05	0.0066514	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737811	GAAGGTGCTGCTGAG[A/G]AAGTAGACGAGCGAC	84900
rs374838340	in-del	-/CTGT			intron-variant	RNFT2	GRCh38.p7	12:116826007	AGGTTTCATCTCTGT[-/CTGT]GCATTTTTCATACAT	84900
rs374875014	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116742160	AAAGCATAGGCCACA[G/T]CCTTTATTGTGTTTT	84900
rs374900190	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805256	TAACAGAGGTAATAG[C/T]GGGCAGTTCTCTCTT	84900
rs374951471	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849844	CTTCCTTCCTTCCTT[C/T]CTTTTTTTTTTTTTT	84900
rs375092573	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116755369	GCCCAGAGGTCTTTT[-/A]TTTTTTTTTTTTTTA	84900
rs375125940	snp	A/G/T	0.0271869	0.113447	intron-variant	RNFT2	GRCh38.p7	12:116821639	GCAAGGAAAAGTCTC[A/G/T]CAGGAGGCTGAGGGC	84900
rs375127266	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116757000	TACCATTTCAATCTC[A/G]CTGCTTGTTATTGGT	84900
rs375135560	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116773735	CATCTCTACATCAGA[G/T]ACAAAATTGTGTAAG	84900
rs375152145	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739866	TTTCTGGCTTCCCCA[A/G]TCAGGACTCTTAGTT	84900
rs375179483	snp	A/C/T	3.82256e-05	0.00437165	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836192	AAAGAACTATGGAGT[A/C/T]CGAGCCACCGGGCAG	84900
rs375215739	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742806	CTTTAAAACTAGCCA[C/T]GTATGGTGGTGCATA	84900
rs375215754	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751467	GGAGTGCAATGGCGC[A/G]ACCTCTGCTCACTGC	84900
rs375224137	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809220	TCATTCATTCATTCA[C/T]TCATCACCTGGGAGC	84900
rs375255080	in-del	-/AAATA	0.5	0	intron-variant	RNFT2	GRCh38.p7	12:116800814	CAAGACTCCATCTTA[-/AAATA]AAATAAAATAAAATA	84900
rs375265047	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116841494	GGCTCACACCTGTAA[C/T]CCCAGCACTTTGGGA	84900
rs375309420	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794680	AGGAAGGAAGGGAGG[A/G]AGGGAGGGAGGGAAG	84900
rs375312021	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811572	GTAGAGACGAGTTTT[C/T]GCCATGTTGGCCAGG	84900
rs375337851	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116749279	TAATCTCTTCCTCTT[-/T]CCCCCCCCACCACCC	84900
rs375373809	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116747981	AGATCACATGAGGTC[A/C]GGAGTTCAATACCAG	84900
rs375397213	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116812968	TGTTTTTGTTTTTTT[-/T]CTTTTGAAACAGGGT	84900
rs375421579	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116794587	TGGGTGACAGAGTGA[G/T]ACTTTGTCTCAAAAA	84900
rs375439137	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116836118	CACAGATCTCACAGT[A/G]CTCCTGAGGGCGTAG	84900
rs375444814	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116808100	TCCCAAATAACTGGG[A/G]TTACAGGCGCCCGCC	84900
rs375473841	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116771697	CCAAATACATGTCCC[A/G]TGATGTGGGCACCCT	84900
rs375474437	in-del	-/ATATA			intron-variant	RNFT2	GRCh38.p7	12:116750847	ATATATATTATATAT[-/ATATA]ATATATATTATATAT	84900
rs375480865	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116820240	GGTCTACAGGCGTGC[A/G]CCATCATGCCTGGCT	84900
rs375521371	multinucleotide-polymorphism	ACT/CCC			intron-variant	RNFT2	GRCh38.p7	12:116803707	GAATGAAATCACCAT[ACT/CCC]CCAGGATGTTCTCAT	84900
rs375545191	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837775	TAGTAACATATCAAC[A/G]TGGGTTTCTTAGCTT	84900
rs375608150	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757510	TATCCCAGAGGTTTT[A/G]ATAGGTTGTGTCATT	84900
rs375617001	snp	G/T	2.57749e-05	0.00358981	intron-variant	RNFT2	GRCh38.p7	12:116740987	TTGGCAATCTGACAG[G/T]CAGTGGGAGTGTTGG	84900
rs375636770	snp	A/C/G	3.29484e-05	0.00405871	synonymous-codon, missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779222	GAAGCCCAACCTGGA[A/C/G]ATGCTGGACTTCTTT	84900
rs375641490	snp	C/T	0.000159987	0.00894249	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750009	CTCCTCGGCTGGCGG[C/T]GGGGACGTGTTCATC	84900
rs375649607	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818406	TAGTAACAGGCCCTG[A/G]CTCAGTGCCTGGTTC	84900
rs375696049	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116741899	CAAGCGATCTTCCTA[C/G]CTTGATCTCTCAAAG	84900
rs375766560	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116793978	TGTGGGCTGAATTCA[A/G]AGTTTCTCTGGGTGC	84900
rs375803308	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116788861	GGATAAATGGGAGGA[C/G]AGTGGATGGATGAAT	84900
rs375817450	in-del	-/CAC			intron-variant	RNFT2	GRCh38.p7	12:116822603	CATCATCATCACCAC[-/CAC]TACTACCACCTGCAG	84900
rs375817842	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116827740	ACTACCTGGTTATTT[C/G/T]TAGAAAAAGTTTGCC	84900
rs375840798	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116848010	CCCTCCCCCAGCCCC[C/T]GCAACAGGCCCCAGT	84900
rs375875941	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790913	CTGCAGTGAACCCTG[A/G]TCGCAGCACTGCACT	84900
rs375894200	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116836855	GAATTGCTTGAACGC[A/G]GGAGGCAGAGGTTGC	84900
rs375987284	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776264	AAACCCAGATAGATG[A/G]ATTGAACACCAACTT	84900
rs375987904	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739969	CCAGCACTTTGGGAG[A/G]CCAAGGCAGGCGGAT	84900
rs375991778	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742553	CGCTGGGATTATAAG[C/T]GCAAGCCACCACGCC	84900
rs376018396	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116758153	AGCTACCCCTGCTTG[C/T]TTTTGGTGTCCATTT	84900
rs376022507	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116834776	CCTAATTTCTCACCT[A/G/T]TGAAGCTCACCATAT	84900
rs376026638	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813259	GAGCCTCCTGGCCAA[A/G]GGAGTCCTTTTGAAT	84900
rs376028373	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831863	CCAGGTGCAGCAGCT[C/T]ACACCAGTAATTCCA	84900
rs376030249	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778026	GAGCTTAGCACAGTT[C/T]CCGGCACATCAGCTT	84900
rs376035842	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116745497	AACTCCTGACCTCAA[A/G]TGATCTGCCCACCTC	84900
rs376040992	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800404	TTGGAAGGCTGAAGC[A/G]GGCAGATCACCTGAG	84900
rs376060936	snp	C/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116760332	TGGAGTCTGCACACT[C/G]GATTTGCACCCTCCC	84900
rs376157196	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825888	ATCCCACGCCTTTAA[A/G]CCACTAGGCTGTCCT	84900
rs376171238	in-del	-/TG			intron-variant	RNFT2	GRCh38.p7	12:116750887	TATATATATTATATA[-/TG]TATAATATATATATA	84900
rs376208903	snp	G/T	6.72834e-05	0.00579976	intron-variant	RNFT2	GRCh38.p7	12:116766775	GAAGGTTCTGCCACA[G/T]GCACCTTTGATATCA	84900
rs376227542	snp	G/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116765436	GGGGCACTGAGCTGT[G/T]TCTGGAGACACTGTG	84900
rs376248570	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116763632	AACAAAAAAAAAATT[A/T]GCTGGATGTGGTGGC	84900
rs376253656	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786416	GCGCCCGGCCGAGAT[C/T]GGGTAGTTCTTACAG	84900
rs376278483	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823536	TAAAAATATGAAAAT[A/G]AGCTGGGCGCCGTGG	84900
rs376279220	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116756315	CTAAGGTTTTTTTTT[-/T]GTTTTTTGTTTTTTG	84900
rs376283123	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754315	ATTCCTTTTTATGGC[C/T]GTGTAGCATTCCACC	84900
rs376300468	snp	C/G			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836589	ACCCCCTGTGGGTCA[C/G]TCACTCTCTCTCTGA	84900
rs376370799	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849845	TTCCTTCCTTCCTTC[C/T]TTTTTTTTTTTTTTT	84900
rs376387074	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116748271	GTTCGTAGGAAACTG[C/T]ACCCAATTCTGGGCT	84900
rs376533510	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765783	GGCTTTGAGAATTAG[A/G]TATATAAGCTTGGAT	84900
rs376541509	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805740	CGGCTTCCCAAAGTG[C/T]TGGGATTACAGGCGT	84900
rs376548421	snp	C/T	2.44215e-05	0.0034943	intron-variant	RNFT2	GRCh38.p7	12:116741021	ACTCTGGCTCACCCA[C/T]GTGTTGGGTTTTAGG	84900
rs376557134	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116806389	AAAAAAAATATATAT[-/AG]ATATATATATAGATA	84900
rs376574265	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116844314	TAGCTCACTGCAACC[A/T]CCACCTCCCAGGTCA	84900
rs376591247	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116829974	AGGATTTTTTTTTTT[-/T]GCATTCTCTATTATT	84900
rs376593118	in-del	-/TGGAGTGCA			intron-variant	RNFT2	GRCh38.p7	12:116821882	AGTGCATGGAGTGCA[-/TGGAGTGCA]GTGGCGCAACCTCAG	84900
rs376649498	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773205	GACCTCAGGTGATCT[A/G]CCCGCCTTGGCCTCC	84900
rs376650532	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116799490	TTAAGATGGGAAATT[C/T]TGCTGGGTGCCCACC	84900
rs376691025	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116755990	GTATAGGTTGAAATC[A/G]GGTAGTGTGATGCCT	84900
rs376718312	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116822373	CTCTGTGGCAATTCC[A/G]GCTGTAAGAGTGTTG	84900
rs376730197	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116743619	ACCTGGGGGCCTGTT[C/T]TCAGATTGGGACAGC	84900
rs376760449	snp	A/G	6.32611e-05	0.00562375	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749884	GCGAGTGTGGATGAA[A/G]GTGGCGTCTTTGAGA	84900
rs376814592	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116789876	ATAGATGGGTGGATG[G/T]GTAAATGGTAGGAGA	84900
rs376855207	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811915	ACCAGCCCTGGACTG[C/G]GTCCTGGGGCTGCCT	84900
rs376877783	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116761019	AGGGAGGCCATTCTT[C/T]GGTCTATCACCCCTG	84900
rs376904333	snp	A/G/T	0.000773968	0.0196569	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779262	TGGATTGTGGGGATC[A/G/T]CAGACTTTGTTCTGA	84900
rs376911182	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750223	CCCGCCCTGTCCGAG[C/T]TGAAGGCTGTGATCT	84900
rs376913056	snp	A/G			utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852445	GTTCCAGGGCAGTGT[A/G]GCATCTTTCAAGCTC	84900
rs376933012	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116809266	TCCCAGTCCTCCTCC[A/G/T]TCAGAGGTTGCGTTT	84900
rs376935571	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832382	TTCACCCATGTCATC[A/G]CGAATCTCAGGCATT	84900
rs376952027	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116788401	CCCACCTGCACCTAC[C/T]GATTCATCTGCCTCA	84900
rs376955759	snp	C/G/T	0.000166236	0.00911549	missense, synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833884	CATCATGGGTGACGA[C/G/T]TCCTCCAACAGCTAC	84900
rs376960900	snp	C/T	4.94556e-05	0.00497246	intron-variant	RNFT2	GRCh38.p7	12:116753981	CCCTTCTCTGTCCCA[C/T]AGGCATTGCTGTGTG	84900
rs376977883	snp	C/T	0.000153988	0.00877327	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836307	GCTCAGGCGGGACCA[C/T]TGGAGACCAAGGCTG	84900
rs376978684	snp	C/G	1.64988e-05	0.00287213	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852753	CAGACCTGGAATTCT[C/G]ATTCCAAACTCTTTA	84900
rs376986188	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808529	CTGGGATTTCCCACA[C/T]CCCACCCTCTACTGG	84900
rs377043417	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116841964	ATATATATATAGAGA[-/G]AGAGAGAGAGAGAGA	84900
rs377106125	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811139	TGGCTCACGCTACTC[A/G]GAAGTTTGTCTTTCC	84900
rs377129932	snp	C/T	2.3894e-05	0.00345636	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737906	GGTTCACCATCCCGG[C/T]GCGGACGTGGGGCGC	84900
rs377154469	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116844217	CTTGTGTATTATGGG[-/T]TTTTTTTTTTGTTTT	84900
rs377169774	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116762056	CGGGTGACAGAGTGA[C/G]ACTGTCTCAAAAAAA	84900
rs377188902	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833724	ACTGCCCGGGGCGGG[A/G]GGCCCCCCAGCTGGG	84900
rs377205083	in-del	-/AAGA			intron-variant	RNFT2	GRCh38.p7	12:116822711	AAGAGGAGAGATAGA[-/AAGA]GAACTGGCTGGGTGC	84900
rs377205522	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116780580	TGGTTTCTAGTTGAG[A/C]CAAAATCCTAGGCTG	84900
rs377294134	snp	G/T	0.000104841	0.00723944	intron-variant	RNFT2	GRCh38.p7	12:116741107	AAGGTAGGCATCCCT[G/T]CTTCTGTTCCATCTG	84900
rs377305571	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783479	GACCACATATGTTGA[C/T]CAGGAATAGGCTGCA	84900
rs377312847	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116768541	TTGCAGCCATCATAA[C/T]GCTGTAGCACAGTGC	84900
rs377441858	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815884	AGATCCACACTTGAG[A/G]ACCCTGTTTGTCAAG	84900
rs377455935	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116790641	TTTGTTTTCTTATTG[A/T]GATACAATTCACGTA	84900
rs377486851	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825152	GCCTCAGTTCTCACC[A/G]TTGGCTGGTTTTCAT	84900
rs377523917	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116743987	ATCCCAGCACTTTGC[A/G/T]GGGGTAAGGCAGGCT	84900
rs377546552	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845205	GCTGTGATCGCACCA[C/T]TGCACTCAAGCCTGG	84900
rs377553232	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116806232	AAAATTAGCCAGGCA[G/T]GGTGGTGCATGCCTG	84900
rs377578957	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116771486	AAAAAAAAAAAAAAA[A/T]AAAAAAAAATACGTA	84900
rs377637137	in-del	-/CT	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116761312	CACCACCACGCCTAG[-/CT]AATTTTGTATTTTTA	84900
rs377667002	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116743760	ACAAATGGTATCCCC[C/T]GGTCCCAGCACTGGG	84900
rs377668559	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116845258	CAAAAAAAAAAAAAA[A/T]ATATATATATATATA	84900
rs377678112	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116794697	GGGAGGGAGGGAAGG[-/G]AAGGGAGGAAAGAAA	84900
rs377692395	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750882	ATATAATATATATAT[A/T]ATATATATAATATAT	84900
rs377695876	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116807423	AATGCTTCATTAACA[A/T]GAACTCATTTCATTC	84900
rs377744600	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841760	CTCAAAAAATATATA[A/T]ATATAAATATATATA	84900
rs377745060	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809303	GATTCCTGGTGGTTC[A/G]GGTGCTGACAGGAGT	84900
rs386377851	in-del	-/TTT			intron-variant	RNFT2	GRCh38.p7	12:116750915	TATATATATTTTTTT[-/TTT]TTGAGACAGGGTCTT	84900
rs386377852	in-del	-/TT			intron-variant	RNFT2	GRCh38.p7	12:116776917	AGCTCAAAATGGGAT[-/TT]TTTTTTTTTTTTTTT	84900
rs386377853	in-del	-/TT			intron-variant	RNFT2	GRCh38.p7	12:116776934	TTTTTTTTTTTTTTT[-/TT]TGAGAAGGAGTCTCA	84900
rs386766714	multinucleotide-polymorphism	AG/GA			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737541	AAGGAGGAGGAAGGT[AG/GA]GGAAGGTAAGGAAGG	84900
rs386766716	multinucleotide-polymorphism	CCCAG/TCCAA			intron-variant	RNFT2	GRCh38.p7	12:116757579	TGATGTCATTTTTGA[CCCAG/TCCAA]TGCTCATTCAGGAGC	84900
rs386766717	multinucleotide-polymorphism	AAT/GAC			intron-variant	RNFT2	GRCh38.p7	12:116779913	CATTGGAGTTCAGAG[AAT/GAC]TGAGCAGGGCTCAGA	84900
rs386766718	in-del	AGA/GG			intron-variant	RNFT2	GRCh38.p7	12:116780684	ACAAAAAAAAAAAAA[AGA/GG]GATGTGGAGAAGAAA	84900
rs386766719	in-del	CCA/GC			intron-variant	RNFT2	GRCh38.p7	12:116780908	ATGTTCAGATCCCAG[CCA/GC]TACGCCTCTCCAGCT	84900
rs386766720	multinucleotide-polymorphism	AAAAAA/GTCTCC			intron-variant	RNFT2	GRCh38.p7	12:116782074	ACAGAGCGAGACTCC[AAAAAA/GTCTCC]AAAAAAAAAAAAAAA	84900
rs386766721	in-del	AA/GAG			intron-variant	RNFT2	GRCh38.p7	12:116794688	AGGGAGGGAGGGAGG[AA/GAG]GGAAGGGAAGGGAGG	84900
rs386766722	multinucleotide-polymorphism	ATG/GTA			intron-variant	RNFT2	GRCh38.p7	12:116808234	CCTCCTAAAGTGCTC[ATG/GTA]AGCCACCACACCTGG	84900
rs397704300	in-del	-/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738395	AACGCGATTTTTTTT[-/T]TCTTTTCTCCCATCA	84900
rs397734228	in-del	-/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116847544	CTCTTTTTTTTTTTT[-/T]GAGGCAGAGTTTTGC	84900
rs397737474	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116762415	AACAAAAAAAAAAAA[-/A]CAAAGAAAGAAATAG	84900
rs397771826	in-del	-/GT			intron-variant	RNFT2	GRCh38.p7	12:116840943	TGTGTGTGTGTGTGT[-/GT]CCTGTCTGGTAGTAG	84900
rs397782811	in-del	-/T	0	0	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738396	ACGCGATTTTTTTTT[-/T]CTTTTCTCCCATCAT	84900
rs397795741	in-del	-/GGAT	0	0	intron-variant	RNFT2	GRCh38.p7	12:116788846	GATGGATGGATGGAT[-/GGAT]AAATGGGAGGAGAGT	84900
rs397830747	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116831210	TACAAAAAAAAAAAA[-/A]GAGAGAGAGAGAGAT	84900
rs397838208	in-del	-/TAAAA			intron-variant	RNFT2	GRCh38.p7	12:116800853	taaaataaaataaaa[-/TAAAA]taaaaaCCATTTAAC	84900
rs398021218	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116744243	AAAAAAAAAAAAAAA[-/A]GAGTTGTTTATGGAT	84900
rs398021219	in-del	-/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116753168	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC	84900
rs398021220	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116763190	AGAAAAAAAAAAAAA[-/A]TCTCATCAGAAAGTG	84900
rs398021221	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116763629	ATAACAAAAAAAAAA[-/A]TTAGCTGGATGTGGT	84900
rs398021222	in-del	-/A	0	0	intron-variant	RNFT2	GRCh38.p7	12:116787733	GAAAAAAAAAAAAAA[-/A]GATATAATGTGTATA	84900
rs398021223	in-del	-/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116793229	TTTTTTTTTTTTTTT[-/T]GAGGCAGGGTTTCAT	84900
rs398021226	in-del	-/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116850336	ATTTTTTTTTTTTTT[-/T]AATTTTTAGTAGAGG	84900
rs398098522	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116803105	GTCTTAAAAAAAAAA[-/A]TCAAAAACAAATACA	84900
rs527270334	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116777131	CCATGTTGGCCGGGC[C/T]GGTCTCAAACTCCTG	84900
rs527301517	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847865	ATTTAATTTTAAGTT[C/G]CAGGATGCATGTGCA	84900
rs527312233	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822211	CAGTCACAGTGCTGC[C/T]CCCATGGTTGTGACC	84900
rs527353654	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116743996	CTTTGCGGGGGTAAG[A/G]CAGGCTGATCACCTG	84900
rs527369272	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742099	TGCTTGCAGGGCCAC[C/T]TGGGGAAGCACCAGC	84900
rs527409015	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116742539	CCCAAGCTCCTGCTC[A/G]CTGGGATTATAAGCG	84900
rs527428791	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116779680	CCGGGACCTGCTTCT[C/T]CCAGGGAAGGAGAGC	84900
rs527451489	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850571	AGATAGCCCAGGCCT[A/G]CAGATTAGAATCCCT	84900
rs527490986	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810139	GCAGACCAGGAGTTT[A/C]ACGCTGAAAGCTCAC	84900
rs527504382	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802796	TACAGGAGCTACAAG[A/G]AACTAATGAACAGGT	84900
rs527513139	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851031	CAAAGCATGCAGCAT[C/T]CTGCTTGGATTACGT	84900
rs527513144	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116844020	ACAGTGGTTCCCAAA[A/G]TGTGGCCAGGGTACC	84900
rs527530547	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757159	TTATATTTCAGTGGT[A/G]TCACTTGAAATATCT	84900
rs527597769	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770319	GTAACAAGCTATGTA[C/G]GTTTGTAATCTAAGA	84900
rs527621820	in-del	-/AAAG/AAG/AG	0.00953873	0.0683987	intron-variant	RNFT2	GRCh38.p7	12:116831209	CTACAAAAAAAAAAA[-/AAAG/AAG/AG]AGAGAGAGAGAGAGA	84900
rs527635176	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809626	GGTTCCTCAAAGACT[A/G]GGCTTCACCCCTGCC	84900
rs527637431	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762223	GTCTCTACTAAAAAG[A/T]TACAAAATTAGCCAG	84900
rs527664791	in-del	-/CT	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116778882	AAAACCACCTCTTTC[-/CT]CTCTATAAGTTACCC	84900
rs527695906	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808346	CCTCCTGCCTTGGCC[G/T]CCCAATGTGCTGGAA	84900
rs527717423	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849207	CGAGTGCAGGCGCCC[C/T]GAAGGCAGGGGTTGT	84900
rs527769008	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116809322	GCTGACAGGAGTTGA[A/G]AAGTGCTGATGAGAG	84900
rs527770088	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816385	CAACTCTTTTGGGGC[C/T]TCAGCCTGGCCCCAA	84900
rs527771677	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813918	CGTATATAATGGGGA[G/T]AGTATTCATGATGTG	84900
rs527773869	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820896	GAGAAACTCATCACT[A/G]AACTAGAAGCCAGCC	84900
rs527831551	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116846622	CTTTTAAAAAAACAT[G/T]TTGTTTAGATTTTTT	84900
rs527843937	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116796421	CTGAATCATCTTAAC[A/T]AAGTTCTAGCTCAGT	84900
rs527856454	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835319	CTGAATGTTTTCTAT[C/G]TCTCTTACCTCAAAA	84900
rs527856988	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842983	TTTCTCGGCTCACGC[C/T]GAACACCAAGTGCTA	84900
rs527857886	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795472	AAGATCCGGGAACTG[C/T]GCTGTCTAATATAGT	84900
rs527860319	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756231	TTGTTCGTGTCATCT[A/G]TGATTTCTTTCAGCA	84900
rs527887429	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741586	GGCACTAATCCCATT[C/T]GTGAAGAGCCCATCT	84900
rs527891492	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116769959	AGAATCATTTGAACC[C/T]GGGAGGCAGAGGCTA	84900
rs527954141	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755444	TCAGGCTCCTTCCCA[C/T]TGGCTCTCACAAAGT	84900
rs527998630	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849619	TCTGACCTTCATCTT[C/T]CTCTCTCGTTCTGTG	84900
rs527998748	snp	C/G/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116842453	GGCGCACAGCTCCCC[C/G/T]TCTCTTGAGTCTCAC	84900
rs528017200	in-del	-/GAGCTC			intron-variant	RNFT2	GRCh38.p7	12:116767447	TGGGCTCGGACCTCT[-/GAGCTC]AGGCAATCCACCTGC	84900
rs528027400	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758803	AAGATTGTTTCCTTC[A/G]TTTTAACTTTGGATA	84900
rs528028073	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766240	TGAGCTATGATCACA[C/G]TACTGTACTCCAGCC	84900
rs528060569	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116852014	GTGGCATGGAGCACC[A/G]TAACCATCTGTGCTT	84900
rs528122217	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116846487	GGTGGAGGAAGTCTC[A/G]CCATGTTGCCCAGGC	84900
rs528128336	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116759732	CTATGGGTCTCTCAG[C/T]CATGGATACCAGTGC	84900
rs528160810	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811114	AAAGGAAGTTATCCA[A/C]CAGGCATGATGGCTC	84900
rs528184135	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851611	CGGGCGCGGTGGCGG[A/G]TGCCTGTAATCCCAG	84900
rs528238089	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752910	TGCATCAGGTGAAAG[A/G]GGAATCCTGTCTACA	84900
rs528238703	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811670	CGTGAGCCAACGCAC[C/G]CGGCATGCGTGCGCG	84900
rs528245236	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116831313	GAATACCACAGAAGT[C/G]ATACTGTGTCTTTTC	84900
rs528249530	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792616	TGTGCCAGGTCAGCG[C/T]GTAATCTAGCCTGTA	84900
rs528306839	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746328	TTGGTCTCCAGTGGG[A/G]TCGGGGCACCTGTCT	84900
rs528319025	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116808109	ACTGGGATTACAGGC[A/G]CCCGCCACCATGCCC	84900
rs528350210	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806043	CCCCCTTTAAACAAG[A/T]GGGCAGCTTTGAAGC	84900
rs528352684	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760238	TTTCCAGGTGGAGAG[A/C]GATAGGGGCTTGAAA	84900
rs528363873	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752420	GAGTATGATCATTTT[A/G]TTTTTCACTTGGCAG	84900
rs528408030	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792307	TGCCCACCTCGGCCT[A/C]CCAAAGTGCTGGGAT	84900
rs528432098	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750953	CAGCCAGGCTGGAGC[A/G]CAGTGGTGCAGGTCT	84900
rs528445164	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775358	CTAGACGGTGCTTGT[A/G]TGTGACACCAACAAC	84900
rs528467946	snp	A/C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116751497	CAACCTCCACCTCCC[A/C/G]GGTTCAAGCAATTCT	84900
rs528478369	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743552	GGATTACAGGCATGA[A/G]CCACTGCACCCAGCC	84900
rs528503282	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838211	AGCTGATAATCTTTT[A/G]TTATTACAAATAAGG	84900
rs528542398	snp	G/T	2.16495e-05	0.00329003	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750229	CTGTCCGAGCTGAAG[G/T]CTGTGATCTGCTGGC	84900
rs528547545	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796526	CTCTAAGCACAGGGA[C/T]GGGGAGGGAAGGTGG	84900
rs528561907	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757853	CATTTGTTCCAAGGT[A/G]TAGTTTAAATCCATT	84900
rs528678890	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116779602	GGTTGTTCACAGCTA[C/T]CCTTGATGCAATTTT	84900
rs528759448	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791783	AATTTTTGTGGTAAA[C/T]ACATAGGCAGAGAAT	84900
rs528773424	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823040	AAAAATACAACTAGA[A/G]AACTAGAGAAGGCTC	84900
rs528783346	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116784878	TTCATTCTTTTCCCT[A/G]CCAGCGGAGCAGGAC	84900
rs528793630	in-del	-/T	0.178465	0.239547	intron-variant	RNFT2	GRCh38.p7	12:116768100	TTGCACAGTTTGGCC[-/T]TTTTTTTTTTTTTTT	84900
rs528817935	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738142	CTCACCATTGGTCCC[G/T]AAGGAACGGCGGCCT	84900
rs528841768	in-del	-/TATTTTC			intron-variant	RNFT2	GRCh38.p7	12:116850613	AAGTATTTTTTCTTT[-/TATTTTC]TCTTTTCTTTTTTTT	84900
rs528870144	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794768	TGCTGTCTAATATAG[C/T]AGCTAAAAAAACAAA	84900
rs528884476	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748362	CTACAGAATCCTTTG[A/C]CTGATTCCAACCCAA	84900
rs528901807	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827468	AAAGAAGCTGGTATT[A/G]GAGCCTTCTGGGAAA	84900
rs528948216	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841545	CTGAGGTCAGGAGTT[C/G/T]GAGACCAGCCTGGCC	84900
rs528953787	in-del	-/GGGTGGAGGGTGGA	0.0482946	0.147699	intron-variant	RNFT2	GRCh38.p7	12:116774770	AGAATGTCAAGGTCC[-/GGGTGGAGGGTGGA]GGGTGGAGGGTGGAG	84900
rs528956192	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800126	AAGCTTCACCAGAGG[C/G]CGAGCATATGCAGGT	84900
rs528963410	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116828306	ATTCTATTTCAGGAG[A/G]TCTGGGGTGAGGCCT	84900
rs528991928	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116824741	GTGGCAGAGAGATCT[C/T]TCATGTCTCTTCCTA	84900
rs529010720	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116777704	CACTGCTGCACCGCA[G/T]GGTCTGTAATCTGTC	84900
rs529033879	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116805672	AGAGACAGGGTTTTG[C/T]CATGTTGGCCAGGCT	84900
rs529037076	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116794380	AGGCAGGCGGATCCC[C/T]TGAGGTCAGGAGTTC	84900
rs529086992	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821485	CCATCCTAACAGGCC[C/T]GCAGGCCACCTTCCC	84900
rs529100776	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814583	AATGAGCCTGTGTGG[C/G]TGGAGCAGAAGAAGG	84900
rs529111916	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777032	AAGTGATTCTCCTGC[C/T]TCAGCCTTCCGAGTC	84900
rs529155436	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116828048	CCAGAGACACAGGGA[C/T]GTTTCATGGGGTAGC	84900
rs529197685	in-del	-/A	0.173965	0.238157	intron-variant	RNFT2	GRCh38.p7	12:116797539	CAGCCTGTCTATCTC[-/A]AAAAAAAAAAAAAAG	84900
rs529298241	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774047	AAATAAGCCAGATAA[A/G]AAAGGACATTAAGTG	84900
rs529306209	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116822346	TCTGTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT	84900
rs529349407	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786965	TGCCTCTCTCTGCCT[C/T]TCTCTTATAAGGACA	84900
rs529368386	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825989	CTTGATACAGAAAAA[A/T]AAAGGTTTCATCTCT	84900
rs529409629	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116826383	ACCGTTTCCCCTTCA[C/T]GGTGGCAGGGAGGCG	84900
rs529444853	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761161	ATTTTTTGTTTTTTT[A/C]TTTTTGAGACGGAAT	84900
rs529446307	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739605	GACCAAGCCCTGCCA[C/T]ATTTAGAGGAGAAAG	84900
rs529456076	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847933	TGGTGGTTTGCTGCA[C/T]CTATCAACCCATCAC	84900
rs529465268	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768391	CAGGCATGAGCCACC[A/G]CACCCAGCCCAGTTT	84900
rs529467755	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116827939	CTGGGGCTGTGCTCT[G/T]GACCACCAAGCCAGA	84900
rs529467840	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800219	CACCTAGTCTCAGCC[A/G]GGCATGGTGGCTCAT	84900
rs529477392	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799664	TCCTCAGCTGGGCAC[A/G]ATGGCTCATGCCTGT	84900
rs529531157	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116802500	AAATCTTAAAATATT[G/T]ACTGTCTGGTCCTTT	84900
rs529532577	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753747	CATCCCCTGATCCAG[G/T]GCTATAAAGTATCCC	84900
rs529569378	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813597	GTGTTTGCTGGTTTG[C/T]CTCCCCCATTAGGAC	84900
rs529615973	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786399	TACAGGCATGAGCCA[C/T]CGCGCCCGGCCGAGA	84900
rs529617693	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807179	AGCAATCTCTGTACC[A/G]GGGTGATTATCCCTT	84900
rs529618212	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770438	CCAGGTCACCTAAGG[A/T]TGTGTTTCTCAGAAC	84900
rs529633326	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116767814	CAAACTCCTGACCTC[A/G]TGATCCACCTGCCTT	84900
rs529649486	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116812566	TTGAGACAGGGTCTC[A/T]CTCTGTCACCCAGGC	84900
rs529676976	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116810322	CATCGCAAAGCCACA[A/G]GGGCACGGCAGGAAG	84900
rs529682248	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778529	TGCCCTTGAACTTTC[C/T]AGCCTGTAGAACCCT	84900
rs529719452	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761544	TCCTCCTGCATGTCC[C/T]CTGTGTCTGCTGAGC	84900
rs529721063	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770997	GCTGAAACACAGCTA[C/T]ACCCATCCATTTACG	84900
rs529773251	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116777728	ATCTGTCCATTATCT[C/T]ATCAAATCCTGCCAA	84900
rs529781826	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816400	CTCAGCCTGGCCCCA[A/T]GGACTCTGCCAGCTG	84900
rs529789914	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116777632	CTGTGCCTCAGTTTC[C/T]TCATCTGCAAAATGG	84900
rs529790507	in-del	-/G	0.00874735	0.0655527	intron-variant	RNFT2	GRCh38.p7	12:116789243	GGAGAGTAGATGGAT[-/G]GGTGGATGGGTAAAT	84900
rs529814049	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844912	ATCTGAGCAAGAACC[A/G]TACTCAGCATAAAAC	84900
rs529829453	in-del	-/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116816458	TCGCGGCCTCCTCCT[-/C]CCCCCTCCTCGCCAG	84900
rs529834561	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797176	TGAACTGTGCTCCCC[A/G]AATGTTATGGACTGA	84900
rs529835209	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822913	GAGGCACGAGAATCA[C/T]TTGAACCCAGGAGGC	84900
rs529887675	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804548	ATTTTTTTACCATTA[C/T]GTATATTACAGTAAT	84900
rs529903253	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810176	GTGGGGGTGTTGCAG[A/G]CAAGGAAGCAGTCAC	84900
rs529910439	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116740168	GCAGTGAGCCAAGAT[C/T]GCACCACTCCGTCTT	84900
rs529924478	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845595	CATGGGTTGAAGGTC[A/G]TGTGGCACGTCAATG	84900
rs529972629	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803517	GCTGACCCCACTTAC[A/G]TCCACTGTATTGTTT	84900
rs529977174	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754614	CACCAGCAGTGTAGA[C/T]GTGTTCCCTGTCCAC	84900
rs529984226	in-del	-/ACCGGGACAGGAATGCGC			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737222	CTCACCCGTGCTGAG[-/ACCGGGACAGGAATGCGC]ACCTCTCCCCACCCT	84900
rs529986056	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763919	CATGTTTATAGCAGC[A/G]CAATTCACAATTTCA	84900
rs529993616	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116763652	GATGTGGTGGCAGAC[A/G]CCTGTAGTCCCAGCT	84900
rs530048222	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNFT2, C12orf49	GRCh38.p7	12:116738345	ACCTGAATGATGCGG[C/T]TGTGATTGCTGAATT	84900
rs530081553	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756344	TGTTTTGCAGCTATT[A/G]TAAAAGGGGTTGAGT	84900
rs530144950	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843134	GATAGAATTTGGGGT[A/G]AGGGTGAGGTGACTG	84900
rs530149850	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762953	CAGGTGTGGGGGCAT[C/G]TGCCTGTCATCCTAG	84900
rs530151734	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769529	GAGGCTAAGGTGTAC[A/G]TTTATGTCTTAAGTT	84900
rs530165234	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116757625	TTTCCATGTGTTTGC[A/T]TGGTTTTGAAGGTTC	84900
rs530182853	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815297	CTGTGTTAGCTTCCT[A/G]TGAGTACTGTAACAA	84900
rs530231229	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790445	TAGATGCTGTTGATA[C/G/T]CTCTTTTCACAGAGA	84900
rs530263283	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116848248	ATCCAGTCTATCATT[C/G]ATAAGCATTTGGGTT	84900
rs530265301	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783894	AAACTCTTAGAGGCC[A/G]CTTAACCGTGTACTG	84900
rs530288508	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742166	TAGGCCACAGCCTTT[A/G]TTGTGTTTTCTGGGG	84900
rs530306684	in-del	-/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116845957	CAGTTAACTGCCAAA[-/T]TGTTCTTCAGGCTTC	84900
rs530308523	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749499	TGCCCAGGCTGGTTT[G/T]GAACAACTAGGCTCA	84900
rs530314082	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116838954	TGTGAGCTAGGCCTG[A/G]AAAGGCAGAGATGAT	84900
rs530339348	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789487	GGGTAAATGGGAGGA[A/G]AGTGGATGGGTGGAT	84900
rs530373311	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835816	AACACTGTTGGGAAG[A/G]AAGAAGTGCAAATGA	84900
rs530398769	snp	C/G	0	0	intron-variant	RNFT2	GRCh38.p7	12:116756968	CCTGAACTTTTTTTT[C/G]TTGGTAATTTTTAAA	84900
rs530405978	snp	A/G	8.2494e-05	0.00642185	intron-variant	RNFT2	GRCh38.p7	12:116836055	GGTGGTCCCCACCAG[A/G]GTCCTGAGAATCAGG	84900
rs530406394	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116843658	CGTTCATCCCTTTCT[C/T]CACATGCTGGAGGCA	84900
rs530437088	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116835352	AGTATCCGTGTTAAA[C/T]TGCACACCCTCAACT	84900
rs530448733	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847652	CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGATTA	84900
rs530464125	in-del	-/TC	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116849798	TTCTTTTCTTTTCTT[-/TC]TCTCTCTCTCTCTGT	84900
rs530502027	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847053	AGCTGGGACTATAGG[C/T]GTGTGCCACCATGCC	84900
rs530517308	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798893	TAACAGTACCTACAT[A/G]TGTTAGTTTTCATTT	84900
rs530520878	snp	A/G	1.64768e-05	0.00287021	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852637	TTTATCGGAAAGATC[A/G]TCCTGCCTGCAGATG	84900
rs530534550	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752992	TGTAGCTTGGCAAAC[A/G]GTGGCAATGAAATGA	84900
rs530587344	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116805506	TTGACACAGCGTCTC[G/T]CTCTGTCGCCCAGGC	84900
rs530588254	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116747145	CACTGCAACCTCCAC[C/T]TCCTGGGCTCAAGCC	84900
rs530589063	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812170	GAGAGGTGGGGCAGA[C/G]ACACACAAAAGAACA	84900
rs530612123	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784161	CAGAGATGCTGTCCA[A/G]TTACTGCACGGGGCA	84900
rs530619377	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809801	CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGG	84900
rs530651608	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116806094	GTTAACAAAGTATTC[A/G]TCTTGGCTGGGTGCT	84900
rs530669532	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799424	CCTTTTATCGTGTAG[A/C]CTGTAATATGATCTA	84900
rs530675740	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116833618	GTGGGCAGGGGCCGC[A/G]TCTCCCTGGCCATAT	84900
rs530681841	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815168	CTCAGAGGCCACTCC[C/T]AGGCCTGGGTGTGCT	84900
rs530695988	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753450	GCCACTGCACCCAGC[A/G]GTGAGTTTTTTCAAT	84900
rs530721688	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786408	GAGCCACCGCGCCCG[A/G]CCGAGATCGGGTAGT	84900
rs530724437	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116793393	GGTCTCACTGTCTTG[C/T]CCCAGGCTGGTCTCG	84900
rs530732334	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739639	TCCAAGGGGAGGGCA[C/T]AGCAAGTGCAAAGGC	84900
rs530740358	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826514	GGAATTATAAAACTG[C/G]TTAATTAGGGAGAGA	84900
rs530748372	in-del	-/ACAACCTCAG	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116808646	TAGAGAAGATGAAAA[-/ACAACCTCAG]ACAATGGAAGACAAG	84900
rs530766637	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838768	TCAGTCTGTTTGTCT[C/G]TCCTCCATTCTTCTC	84900
rs530798107	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758310	TGGAGCATTTAGGCC[A/C]CTTACATTCAATGTT	84900
rs530815654	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116764308	TCACCACAAAAGAAC[G/T]TATTCATGTAATACC	84900
rs530826850	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116746415	TCTCAAGGGAAAGAT[A/G]AGGAATAAAATAACA	84900
rs530828174	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116824091	CTGCACCCAGGGCCA[C/T]GTTTCTTTCCCAGGT	84900
rs530856900	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739388	CAGTGTCCTGGATGC[C/T]GAGGCAGAGGGGTGA	84900
rs530862785	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761132	GCAGACATTCAGCTC[A/G]TTAGCTCACTTTCAT	84900
rs530904069	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744383	CATGAGATCTCTTGC[A/G]GGCAGAGAGCACAGC	84900
rs530927805	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792207	GCTGTGCACCACCAC[A/G]CCCAGCTAATTTTTG	84900
rs531018275	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819012	GTTCCTGCGCCACCC[C/T]TCCCTACGTGGGTAA	84900
rs531050983	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116852236	AATCTGTGTGGCTAG[G/T]GGGCAGATTACCATG	84900
rs531055875	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766501	AACTTGCCTGGAGTT[C/G]GACAGCTCCCACACA	84900
rs531070419	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116751962	TTACTTATTAGATCA[C/T]GGTGTTGCTGTGCCC	84900
rs531092747	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116772919	CTGTAACCTCCGTCT[C/G]CTGGGTTCAAGCAAT	84900
rs531103530	in-del	-/TA	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116770424	GTTCACACAAGGACC[-/TA]AGGTCACCTAAGGAT	84900
rs531106681	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738670	ATGTACAGAGCAGAG[A/G]ATTAAAAAGCGTTTC	84900
rs531169932	snp	C/T	0.000725438	0.0190314	intron-variant	RNFT2	GRCh38.p7	12:116835929	AGTGATCCTTGGGTA[C/T]ATTTCAGCCACCACC	84900
rs531227554	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828590	GTTATCTTAGTACCT[A/C]CAGAACCTGGCATTG	84900
rs531287428	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116818611	AACTGGGTTTGATGG[C/T]GACCCTGTCGGAGAG	84900
rs531334915	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116743588	TTTATATCTATTGAA[A/G]CCCAAGAGGGAACAC	84900
rs531339805	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116740996	TGACAGGCAGTGGGA[A/G]TGTTGGGAGACTCTG	84900
rs531448679	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849796	TTTTTCTTTTCTTTT[A/C]TTTCTCTCTCTCTCT	84900
rs531481573	in-del	-/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116779922	TCAGAGGACTGAGCA[-/G]GGCTCAGACAAGGTA	84900
rs531491086	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821543	CTTGTCCTGGCCGCC[C/T]ACTTGGGAGCAGGAC	84900
rs531537529	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816070	CTATAGCTGACTTGG[C/G]GACAGATAAGCTCAT	84900
rs531541062	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116849555	ACTTACATCCTGCCT[C/G]TTGCCCTCCACCACC	84900
rs531542648	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809258	TGGCTGCATCCCAGT[C/G]CTCCTCCATCAGAGG	84900
rs531612664	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813664	ATATTTCATTTTATT[A/C]CCAGCACAGTGCATG	84900
rs531616421	snp	A/G	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116769774	TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	84900
rs531629650	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841546	TGAGGTCAGGAGTTC[A/C/G]AGACCAGCCTGGCCA	84900
rs531643597	in-del	-/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737540	GAAGGAGGAGGAAGG[-/T]GAGGAAGGTAAGGAA	84900
rs531657234	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777105	GTATTTTTAGTAGAG[A/G]CAGGGTTTCACCATG	84900
rs531687481	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767926	CTGGTATCTTACATA[C/T]ACAGCTCATGTCAGT	84900
rs531693676	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116843173	CCAATTCTGTGCTTC[A/G]GGAGGCACGACCAGG	84900
rs531703580	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116840522	AATAGTCTCTGCTGT[A/G]TCCAGCCAGGCCTGT	84900
rs531716296	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116781860	GGCGGGTGGACTGCC[C/T]GAGCTCAGCAGTTCA	84900
rs531744916	in-del	-/TA			intron-variant	RNFT2	GRCh38.p7	12:116791264	TCTCTCATGCCGTGC[-/TA]TGTTTTCGAGGTTCA	84900
rs531754254	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820367	GTTTATAGGTGTGAG[A/C/T]CACCATGCCCAGCTA	84900
rs531780398	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800711	CCCAGCTACTCAGGG[G/T]GCTGAGGCAAGAGAA	84900
rs531785487	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116849114	CTGAGCCACCACACC[A/T]GTCCCCTCCCCTGCT	84900
rs531809600	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819818	ATTTTTACAAACATA[C/T]GTAATCACTCAGATC	84900
rs531816805	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827282	GTCTTCAAAGGTGTA[C/T]ATAACAGGAGCACCT	84900
rs531852436	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116807852	TGTGTCACCCAAACC[A/G]GTGTGCTTTGATGCG	84900
rs531905958	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841575	CAACATGGTGAAGCC[C/T]GGTCTCTACTAAAAA	84900
rs531912007	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800159	CATGCTCCCCCTACA[G/T]TCTGCAGAACCATGA	84900
rs531913078	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754413	TGGGTTGGTTCCACA[A/G]TTTTAAAATTGTGAA	84900
rs531916643	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116794464	TTAGTCAGGTGTGGT[G/T]GTGCACACCTGCAAT	84900
rs531941617	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748016	GCCAACGCGGTGAAA[A/C]CCTATCTCTCTAAAA	84900
rs531950104	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116846436	CCACCATGCCCAGCT[A/G/T]ATTTTTTTTTTTTGT	84900
rs532003192	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116789941	GAGGAGAGTGGATGG[A/T]TGGATGGTGGATGGG	84900
rs532041572	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848449	GCTCCAAGCCCTACC[A/G]TGGGCCCCTTACTTC	84900
rs532091353	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817051	GGAGTCTCGCTCTGT[C/T]GCCCAGGCTAGAATA	84900
rs532094033	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771873	AAGTTCTTTTGAAAC[A/G]AGACGCTTCCTCCAC	84900
rs532134606	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766365	CTTGAGGTTTCTTAA[C/T]CTCTCTGTGCTTTAG	84900
rs532154063	snp	C/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116810318	CAGGCATCGCAAAGC[C/G]ACAAGGGCACGGCAG	84900
rs532156462	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116798212	GCCTGGGAAACAGAA[C/T]GAGACTCTGTCTCAA	84900
rs532230220	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116816503	GATCTTTATAGGAAA[A/T]TGGGGGTGAGAGGGA	84900
rs532245099	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804641	GAATTTTAGGATTGA[A/G]TAGCTTTAGCTTTAT	84900
rs532314692	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845725	CTTGCTGACCCCTGG[A/G]TCCTGCCCTCCAGAC	84900
rs532315813	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797838	GTAGATTAAGGGGCA[A/G]TTTATGCAGAAATTT	84900
rs532319394	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751684	GGGATTACAGGCGTG[A/C]GCTACTGTGCCTGGC	84900
rs532343154	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757068	AAGGGTTGTATTTTT[C/T]CAGGAATTTATCCAT	84900
rs532357104	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116752275	TGGTGACTGCCAGCT[C/T]GCTCAGATTCCTCCA	84900
rs532419192	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116781737	AATCACATCAGCAAA[G/T]TCTCTTTTGCCACAG	84900
rs532432492	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758755	ATGGGTTTTCCTTTA[C/T]AGGTTAGCTGGTGCT	84900
rs532437062	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836712	GGCAGATCACCTGAG[C/G]TCAGGAGTTCGAGAC	84900
rs532476827	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791744	CTGCTGTGAGCTTTC[A/G]CAGACAAGTATCTGT	84900
rs532563379	snp	A/C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116784360	GGTCTGATTGGCCCC[A/C/G]GTCATTTTGTGTACC	84900
rs532587750	in-del	-/TTTTT	0.39709	0.20215	intron-variant	RNFT2	GRCh38.p7	12:116850149	CGTGCCCAGGCTCAC[-/TTTTT]TTTTTTTTTTTTTTT	84900
rs532620166	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809585	AGATGGTCAGTTCCC[A/G]ATTCAGACATCCCGG	84900
rs532620532	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801864	TCTCACTCTGTTGCC[C/G]AGGCTGGAGTGCAGT	84900
rs532621243	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116764059	TTCGCAGCAACCTGG[A/G]TGGGATTGGAGACTA	84900
rs532714785	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830117	GCAAAAGTAATGCTG[C/T]GAGTTCCCATATACC	84900
rs532716375	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116810616	CCAAACTACATCATG[C/G]GTATGTGGTGGCAAC	84900
rs532723942	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737354	GAGGAAGAACGAAGT[C/G]AGGAAAGAGGATGTC	84900
rs532741032	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753503	ATCTGATTCTATCAA[C/T]CAGATTCTTTTTAAA	84900
rs532744164	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825451	TCTGGATTATCATGA[A/G]GGCCAGTACTAGCTG	84900
rs532757180	snp	A/G	0.000125581	0.00792304	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737771	AGGGAAGGGGAGGAG[A/G]GGAAGGGCGGCCACT	84900
rs532766235	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747257	GACAGGTTCTTGCAA[C/T]GTTGCCCAGGCTGGT	84900
rs532773250	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116822983	GGTTGGGCGATAGTG[C/T]GAGACTCTGTCTCAA	84900
rs532809535	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796974	TTGGCACCATTGGAG[G/T]GGGTGTGCTACTGGT	84900
rs532823558	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116841508	ATCCCAGCACTTTGG[A/G]AGGGTGAGGCAGGCG	84900
rs532858721	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116807118	AAGCAAAGATTGAGA[C/T]GCTTATTTTGAAAGA	84900
rs532871185	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847762	AAACTCCTGACCTCG[A/G]GTGATCCGCCCACCT	84900
rs532886738	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842256	AGAAGGGACACCCCA[C/T]CACCTTCACTGTATC	84900
rs532909843	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840844	TACCGATATTCAGTA[C/T]TAGTGTTTAATTCTA	84900
rs532936672	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116828074	GTAGCCGTGTCCTTA[C/T]CTGTCATGAGACCAG	84900
rs532973059	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781928	CTAAAAATACAAAAA[A/G]ATTAGCTGGGCGTGG	84900
rs532977937	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833675	GTGCTTTCCAGAGCT[A/G]ATTAATGGCCTGCCT	84900
rs532989633	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775490	TGAGCTTGAATCTTC[C/T]CAGGATTTGATGTCT	84900
rs533029880	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799064	CAGGCTGGGCTCTTA[C/T]CTGGAGGTTCTGGAG	84900
rs533055746	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747945	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	84900
rs533061358	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781508	GTGGGTTTTACTGCG[A/G]TGAAAACAGAAGTTT	84900
rs533082689	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787645	CATTGAGCCCAGGAG[C/T]TGAGGTTGCAGTGAG	84900
rs533102705	snp	C/T	0.0023933	0.0345097	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740384	CTGACTGTGCATCCC[C/T]CTGGAGACGAAGAGG	84900
rs533185592	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820396	TATCCCTGTGTATTT[A/T]AGACTTTCAGTACAT	84900
rs533202174	in-del	-/A	0.000196325	0.00990576	intron-variant	RNFT2	GRCh38.p7	12:116833944	AGCCTCTGCAAGGTG[-/A]AGGTGGCCCCAAGGC	84900
rs533230235	snp	A/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116794367	CTTTGGGAGGCCAAG[A/G]CAGGCGGATCCCTTG	84900
rs533245859	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739801	CTATGGACAGAGCTC[A/C/G]GGTTTGATTCTGATT	84900
rs533246796	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832047	GAGGTGGAAGGATTG[C/T]TTGAACCTGGGAAGT	84900
rs533259601	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116826594	TCAAAGTGGCCCACC[C/T]CCGGCAGCTAATTGC	84900
rs533289312	in-del	-/ATA			intron-variant	RNFT2	GRCh38.p7	12:116750849	ATATATTATATATAT[-/ATA]ATATATATTATATAT	84900
rs533316016	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116819947	TGACTTTAATTTTAA[C/T]ACTATATTTTATTTA	84900
rs533356619	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780326	GGTTTCGGAATGAAA[A/C]TGTTCCACTTCAGAT	84900
rs533400414	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780723	AGGGAAAACAACAGG[C/T]CTAGGGAAGTCCTAA	84900
rs533408252	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116767764	TTTGTATTTTTAGTA[A/G]AGACAGGGTTTCACC	84900
rs533412155	in-del	-/AG	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116779004	AGGGAACTAAGACTC[-/AG]AGAGGTTAAAAGATC	84900
rs533434187	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116770631	TGGTGTGATCACACT[C/T]ACTGAAACCTTGACC	84900
rs533529973	snp	A/C	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116767460	CTGAGCTCAGGCAAT[A/C]CACCTGCCTTGGCCT	84900
rs533561087	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772149	CTAGCTGGAAGGTAG[C/T]GGTGCCATCATGGCT	84900
rs533574750	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806234	AATTAGCCAGGCATG[A/G]TGGTGCATGCCTGTA	84900
rs533575668	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808727	TTTTCTATTGAACCA[A/C]ATGATACTGTTTGTT	84900
rs533579407	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763146	TAGGAAACATTTAAT[C/T]GAGCTAGTTTTCAAA	84900
rs533584064	snp	A/C/G	0.000364914	0.0135037	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849382	CCCGCTCTGCCGCTC[A/C/G]GTCGCCGTGGACACC	84900
rs533638512	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116821088	GTAAGCGCTTAATAC[A/G]GGGGTTACTCTTCCC	84900
rs533656004	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116742600	TTTAGTTTGGTGTCT[C/G]GCCCTAGATGATTTA	84900
rs533657856	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819048	GGCAGATTCCTTTAT[C/T]CCTCTGATCCCGTTT	84900
rs533689556	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116773933	GGATAAACACCCTGC[A/C/G]GTATGTACATACAGT	84900
rs533698309	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116794393	CCTTGAGGTCAGGAG[G/T]TCGAGACTAGCCTAG	84900
rs533747786	in-del	-/TCTTTC	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116820614	ATAGCTTGTATCTTT[-/TCTTTC]TCTTTCTCCCACATC	84900
rs533758033	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769302	GGCAGAGGTTGCAGT[A/G]AGCCGTGATCACGCC	84900
rs533777231	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749710	TCCTGGGAGGAAGGA[C/T]TTCATGTGAATTTGA	84900
rs533778630	snp	A/G	0.000101312	0.00711658	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836250	GCCATCTGTCAGGCC[A/G]AGTTCCGAGAGCCTC	84900
rs533790798	in-del	-/CCAGT	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116780542	GGCCACAGTCTAGTA[-/CCAGT]CTTCAGCCCCAGGAC	84900
rs533839294	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849956	TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCGAG	84900
rs533857573	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755829	TTCTAAAAGGCCTAG[A/G]GAACATATATCGGGT	84900
rs533872907	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116822173	AGCCCTCCTCTCTGT[A/C]CCCTTAGTTCTGATG	84900
rs534006550	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116771199	GGTGCGTTGGCTCAC[A/G]CTGTAATCCCAGCAC	84900
rs534074779	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799806	AGTCCAGTGATGAAA[A/G]TGATGGCCTGGATAA	84900
rs534080778	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116827697	TAGTGGTGCCACAGA[C/T]CGTATGGCCTGCAAA	84900
rs534092869	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116780671	AAATGGCATAAAGAC[-/A]AAAAAAAAAAAAAGA	84900
rs534106533	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116740929	CCAGAGAGCACTAGG[G/T]GTCTAAGATACGACT	84900
rs534106628	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795267	ACAAAAATTAGCCGG[C/G]TGTGGTGGCATGTGC	84900
rs534107653	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116763774	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAG	84900
rs534108504	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782004	GAATTGCTTAAACCC[A/G]GGAGGCGGAGGTTGC	84900
rs534145651	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801968	CTGGGATTACAGGCA[C/T]CTGCCACCATGCCCA	84900
rs534152208	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848570	TCCCTCTCCCATCCA[C/T]CCCAACAACCCCAGC	84900
rs534164788	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841349	TCCCAGCTACTCAGA[A/C]TGCTGAGGTGAGAGG	84900
rs534175040	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116794495	CCCAGCTACGCGGGA[A/G]GCTGAGGTGGGAGGA	84900
rs534215471	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837673	ACTAAACACAGTCTG[A/G]GACCTGGGTTGGATC	84900
rs534224406	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116754449	CTGCTATAAACTTGC[A/G]TGTGCAAGTATCTTT	84900
rs534262732	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739179	CACCCTATATCCACA[A/G]TATTGGCTCTGCCTC	84900
rs534264308	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116787878	CACTCCCTTACTCTT[A/T]CTCTGTTTTTTGTGC	84900
rs534281122	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116777197	TGCTGGGATTACAGT[C/T]GTGAGCCACCGTGCC	84900
rs534285009	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791583	CCAAAGTGCTGGAAT[C/T]ACAGGCATGAGCCAC	84900
rs534347946	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830561	CCAAAGTGTTGGGAG[C/T]ACAGGTGTCAGCCAT	84900
rs534458718	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787364	TGTGAGCATTTTCCT[C/T]CTGCAGAAAATCGAG	84900
rs534556759	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791869	CACAGTGCCTGCACC[A/G]TTTCACATGCCCAGC	84900
rs534563591	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837929	ATAAAAAGTTTACTT[A/T]AAAAAAAATCTTTGA	84900
rs534564530	snp	C/G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116751273	GCCTGAATTGAAATA[C/G/T]TCAACACAGCAAATG	84900
rs534596632	snp	C/G	0.00636936	0.0560724	upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738016	GGCAGGCGCCGGCCC[C/G]GCCGCCCGCAGCCCA	84900
rs534610898	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828782	GATGGGTGGAAGAAA[A/G]AAAGGTAAGGAAGGA	84900
rs534632861	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838464	TTTGACAGTTATTGC[C/T]AAACTGCCCTCTGTA	84900
rs534675461	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116777446	TGTTGTCTGTCTCCA[A/G]TGAGTTAAGTACAGA	84900
rs534677182	in-del	-/GGCCCCAA	0.00278634	0.037221	intron-variant	RNFT2	GRCh38.p7	12:116833949	TCTGCAAGGTGAGGT[-/GGCCCCAA]GGCTGGAGGGCCGGC	84900
rs534680888	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736755	TTTGGGTAAGATTTC[C/G]CCACCCGTGCTCCTT	84900
rs534732827	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758232	TGTTAGGTGAGTCAC[C/T]TGAAGGCAGCAGATG	84900
rs534759460	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116803258	TGGGTGCAACCGACA[C/T]CACCTGCCACGGGGG	84900
rs534764166	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116776113	GACAATAAAATATAT[C/G]AGTCCATTAAAGTTT	84900
rs534783147	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	RNFT2, C12orf49	GRCh38.p7	12:116738321	TGCGCGGGTGATTGG[C/T]TTGGCTGGACCTGAA	84900
rs534890666	in-del	-/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738881	ATTTGCAATGTGGGA[-/T]TAATGGAGGGAGGGG	84900
rs534900011	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116744736	GTCAGGCTGAAATCT[C/T]GGCTGGATGCAGGGG	84900
rs534918141	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764834	GAGGCGGAGGTTGCA[A/G]TGAGCTGAGATTGCG	84900
rs534957999	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785388	GCCTCAACCTCCCGG[A/G]CTCAAGTGATCCTCC	84900
rs534968683	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822024	ATTTTTGGTAGAGAC[A/G]GGATTTCACCGTGTT	84900
rs534993276	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784116	CAGGCCCCTGAGTCT[A/G]AGCTCTTAATCTGTC	84900
rs535053369	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739887	ACTCTTAGTTTGACA[A/G]TAGGATGAAATACAA	84900
rs535057017	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826704	TATTCTCTCTTCAGC[A/G]TTTCAACTCTCCTCC	84900
rs535109004	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836816	ACACCTCTAGTCCCA[A/G]CTACTCTGGAAGCTG	84900
rs535156958	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747399	GAGCCAATTGCAGTG[A/G]CACATGCCTATAATC	84900
rs535161448	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773380	ATTCTTCCTTTAGGC[A/G]TTGTTCCATGCAGGG	84900
rs535163261	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790690	GGCTGGGCTCAATGG[C/T]TCATGCCTGTTATCC	84900
rs535173990	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796042	GCCTCCCAAGTAGCT[A/G]ATATTACAGGCGCCC	84900
rs535230251	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761497	TGGCCATTCCTCTTA[C/T]GCTGCTGGGTGGACA	84900
rs535262061	snp	C/T	0.137527	0.223271	intron-variant	RNFT2	GRCh38.p7	12:116768738	TATTTTTCTCTCTCT[C/T]TTTTTTTTTTGAAAC	84900
rs535292972	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116807958	ACAGGTGTGCACCAC[A/G]CTCAGCTAATTTTTT	84900
rs535295570	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762427	AAAACAAAGAAAGAA[A/G]TAGTGCATACAAGGT	84900
rs535301902	in-del	-/TATG	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116750786	ACATTATTTTTACTA[-/TATG]TGTGTGTGTATATAT	84900
rs535309110	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116826005	AAAGGTTTCATCTCT[C/G]TCTGTGCATTTTTCA	84900
rs535328122	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848613	TCCTTCCTGTTCCTC[C/T]CGCACATCAAACACA	84900
rs535376996	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824071	TGAAGAGGCAGAGCT[A/G]GGATCTGCACCCAGG	84900
rs535395896	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116819592	CGCGCCGCCAGGAGG[A/G]GGATTAATGGCTGCC	84900
rs535414771	in-del	-/ACACTAA	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116756486	TAGATGGCTTTTATT[-/ACACTAA]GGTATGTCCCTTGTA	84900
rs535429738	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774427	CCTGTAAGCAGAATA[C/T]ATTTAGCTTCATTTA	84900
rs535459512	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812334	CACGTTGAGTGACAA[C/T]GCAGAGATGCAGGCA	84900
rs535476589	in-del	-/A	0.0471551	0.14613	intron-variant	RNFT2	GRCh38.p7	12:116763803	AGGGGGCGGGGGGGG[-/A]AAGAACTAAAAGTAG	84900
rs535580301	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116798909	TGTTAGTTTTCATTT[A/C]CTGCCTAACAAATGA	84900
rs535591229	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811841	GCTAAGATCAGAACC[C/G]TGAATGGAAGGAAGG	84900
rs535641524	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799886	CATGGTAAAAAGTGA[C/T]TCCCCATTGTTGGAG	84900
rs535697907	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746603	GGGTTAGGGGAGACA[A/T]CCGGTGAAGGTGATA	84900
rs535727209	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813243	CTGGGATTACAGGTG[A/T]GAGCCTCCTGGCCAA	84900
rs535746629	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116839392	TGGTTGGGTGGGTGG[A/G]TGGATGGATGGATGG	84900
rs535783311	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807422	AAATGCTTCATTAAC[A/G]TGAACTCATTTCATT	84900
rs535790429	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760595	GAAACTTCTCCTGCA[A/G]ACAGACCTTCAGCTT	84900
rs535840346	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766765	GTACATTCTGGAAGG[A/T]TCTGCCACATGCACC	84900
rs535843983	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116805756	TGGGATTACAGGCGT[C/G]AGCCACGGTGCCCAG	84900
rs535856976	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116744692	GTTGGAAGCACAGCC[C/T]CTGTCCCCCTAAGGA	84900
rs535873477	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116759941	ATGGCCTTTGTCTTC[C/T]GCTACCAGGGTGGGT	84900
rs535882519	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116767513	CAGGTGTGAGTCGCC[A/G]CACCTGGCCCCGAAA	84900
rs535935071	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768536	TGATATTGCAGCCAT[C/T]ATAACGCTGTAGCAC	84900
rs535958068	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773123	TGAGCCACCACGCCC[A/G]GCCAATTTTTCATAA	84900
rs535958125	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116765911	AGATCTGAATCTTCT[A/G]CTGGGTTGTAAACTC	84900
rs535983291	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809350	GAGGAGAGGTCCTTC[C/T]ACTTCGTTGTGAGGT	84900
rs535999023	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116771016	CATCCATTTACGTAT[C/T]ATTTATGAGTTCATC	84900
rs536012813	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116836886	AGTGAGCCGAGGTCA[C/T]GCCACTGCACTCCAG	84900
rs536014006	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765123	TTAGTAAGCTTAGGC[A/G]TCGCAGCTGATTAGG	84900
rs536116471	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795809	ACACAGCTGGAGTCA[A/G]CGAAACTGGGGTCAA	84900
rs536185862	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116850908	AGAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA	84900
rs536208920	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748223	GAAAAGAGGATGAAC[A/C]CGAGAATAGAAAGAT	84900
rs536213603	snp	A/T	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116763785	CTCCATCTCAAAAAA[A/T]AAAGGGGGCGGGGGG	84900
rs536299053	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116764316	AAAGAACTTATTCAT[C/G]TAATACCACCTGTTC	84900
rs536331864	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116756534	TGAGAGTTTTAATCA[A/T]AAAGGGATGCTGGAT	84900
rs536372871	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769792	ATCCCAGCACTTTGG[C/G]AGGCCAAGGTGGGTG	84900
rs536395226	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794527	TGCTTGAACCCGGGA[A/G]GGGGAGGCTGCAGTG	84900
rs536419640	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845647	GAGGATGGGGCTGGA[C/T]GGGAGACGGGCCATC	84900
rs536434504	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116790771	ATACCAGCTTGGGCA[A/G]CATGGTGAAACCCTG	84900
rs536444940	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776612	CAAAATAACCCAGAC[C/G]AATCCGTTCTTAGGA	84900
rs536454530	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116832348	CTGTCTTCTTTGATT[C/T]GACATAATGTTTGTG	84900
rs536514020	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802867	TGGGAGGCCGAGCCA[A/G]GAGGATCACTTGAAT	84900
rs536528012	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782021	GAGGCGGAGGTTGCA[A/G]TGAGCCAAGATCGCA	84900
rs536533073	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116757259	TATCAGTTTTATTTA[G/T]CTTTTCAAAGAATCA	84900
rs536534263	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828247	TAGTGCTTCTCAAAC[G/T]TGGATGTGCACTCGG	84900
rs536540988	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116751464	GCTGGAGTGCAATGG[C/T]GCGACCTCTGCTCAC	84900
rs536587659	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116838007	TATATTTATACACAC[A/C]CAAACATATTTTTTT	84900
rs536604143	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755503	CTTGAGTTGAACCCA[A/G]GTACCTTTCTCTTCC	84900
rs536611993	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842525	GCACATAAAGAACAT[G/T]GGCAGGGCCTGGTAT	84900
rs536632010	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785501	CTCACTTTGTTGCCC[A/G]GGTTAGTCTTGAACT	84900
rs536688543	snp	C/T	7.65004e-05	0.0061842	intron-variant	RNFT2	GRCh38.p7	12:116741100	CACCTGAAAGGTAGG[C/T]ATCCCTGCTTCTGTT	84900
rs536693401	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116748855	TCCCCTGCTCCATCC[C/T]TTACCAGCTCTGTGA	84900
rs536745179	snp	A/C	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116841963	AATATATATATAGAG[A/C]GAGAGAGAGAGAGAG	84900
rs536758528	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814049	TAAGCAGAGGAAACG[A/G]GGCCTTGGAAAACAT	84900
rs536804123	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828707	GGGCAGAGGAAAGGG[A/T]AGGAAGGCAGCATCA	84900
rs536804677	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116826123	AGGTGCGTTCTTCCA[A/G]AAAATTCTCCTCTCT	84900
rs536867836	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811936	GGGGCTGCCTGGTTT[G/T]AATCCTGCCTTTGCC	84900
rs536870280	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821684	GAGGCTGGAAGCAGT[C/G]CCTCCTGCTTATTTT	84900
rs536879903	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769341	CCAGACAGAGTGAGA[C/G]TCCGTCTTAAAGTTA	84900
rs536918220	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116785884	TGAAACCCTGTCTCT[A/G]CAAAAAATACAAAAA	84900
rs536928178	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116741639	GCCCACCTTCCAATA[C/T]GATCAAATTACAGGT	84900
rs536997788	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116781610	CTCCCTCCCCCTACA[C/G]CTCTGCCTTCATTGT	84900
rs537011690	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761289	CAGTAGCTGGGACTA[C/T]AGACACACACCACCA	84900
rs537017253	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744916	CACGGAGAGAGAGTG[A/G]CCTCCTCATGGACCA	84900
rs537018515	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839118	CTGGCTATATGGTCT[C/G]ATAGATGCCTGTGTT	84900
rs537059624	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778792	GAGGTGGAGGTTGCA[A/G]TGAGCCGAGATCATG	84900
rs537077895	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116832422	TTATTGCTGGACAGT[A/G]TCCTGTTGTATAAAT	84900
rs537107075	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797936	TTTTGCCATGGCAAT[A/G]GTAAACTAACATGGC	84900
rs537133836	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751874	AAGTGATTCTCAGCC[C/T]TAACCTCAAGTGATC	84900
rs537138964	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830313	TTGTTTTCGAGACAG[G/T]GTCTTACTCTGTCAC	84900
rs537161890	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778207	TAGAGGGGACTGTTA[C/T]GGTTGGGTTTGTCCC	84900
rs537197150	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116752854	CTGCACTCCAGCCTG[A/G]GCGACAGAGTGAGAC	84900
rs537204729	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765586	CAGAGGGATCTGCCT[A/G]TGTGTCCCAGGGTAC	84900
rs537209993	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116818753	ACAAGTCCCAGTTCT[A/G]CAGCAAGTAACTTGA	84900
rs537287464	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766977	CTGGGCTTGGGGCAC[A/G]TACCCTTTCACTTGA	84900
rs537294428	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758925	AGCAAGGCCGGGGAC[A/G]TTTTCCTCGATTATT	84900
rs537323164	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116817875	GTGTTGGGGATAAGA[C/T]GATAAATGAAAGAAA	84900
rs537349314	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825627	GTTAAATCATTGGTA[A/G]CTTGAAGCTGGCCTT	84900
rs537366273	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851366	CCGCTATCCCCAGCA[A/G]AGCCCGCACTCTTAA	84900
rs537386496	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829198	ATATTCTGCAGATCT[C/T]GGGGTCTGCAGCAGG	84900
rs537405625	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823158	TCCTTCTTTGTGGAA[C/G]CTACTTCATGTTAGC	84900
rs537414308	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776151	AATTTAGAAATGATT[A/G]GACTTGATGATGAAT	84900
rs537453296	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778894	TTTCCTCTATAAGTT[A/G]CCCAGCCTAAGGTAT	84900
rs537469921	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116817204	TTTTAGTACAGATGG[A/G]GTTTCACGATGTTGG	84900
rs537517530	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844385	GGGATTACAGGCACA[C/T]GCCACCATGCCCAGC	84900
rs537608927	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754836	TTTGATGGGATTGTT[A/T]GTTTTTTTCTTACTG	84900
rs537617828	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829355	CCCCCCATCTTCCCA[A/G]AAGTTCCAGAGGGAA	84900
rs537628668	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851615	CGCGGTGGCGGGTGC[C/T]TGTAATCCCAGCTAC	84900
rs537633828	snp	C/T	0.000104564	0.00722988	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849347	TGCCTCTGCCTGTGG[C/T]TGGACCGTGAGCGCA	84900
rs537652630	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814693	ATTTTTTTTTTTTTC[C/T]GACAGAGTCTCACTC	84900
rs537695690	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755573	AGGAAGCTATCTCGG[C/T]TCTCAGAGTGCTTAA	84900
rs537695905	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842667	CAACCTCTGCCTCCC[G/T]AGTTCAAGCGATTCT	84900
rs537721544	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810565	AAGCAGGGAGACTCA[C/T]GTTCTTGGCTCCGAG	84900
rs537773807	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762556	AGTCTGGGCAACATA[A/G]CAAGACCCCTTTCTT	84900
rs537855182	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116837403	GACTGAGGCAGAGAG[C/T]GATGAGTTCCAGGTT	84900
rs537857637	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116786363	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	84900
rs537899972	snp	C/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116848024	CCGCAACAGGCCCCA[C/G]TATGTTGTTCCCCTC	84900
rs537919030	snp	C/T	0.00636936	0.0560724	intron-variant	RNFT2	GRCh38.p7	12:116751466	TGGAGTGCAATGGCG[C/T]GACCTCTGCTCACTG	84900
rs537928242	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116784675	CACATCAATAACCTG[A/G]AAAGGACCTCTAACT	84900
rs537941882	snp	C/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116820052	GTTTTTCTAAGACTT[C/T]GAAATTCCTTGTTTC	84900
rs537947773	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781982	TACTCGGGAGGCTGA[C/T]GCAGGAGAATTGCTT	84900
rs537954251	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116775058	CCTGAGGTCAGGAGT[C/T]TGAACCAGCCTGGCC	84900
rs537992003	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806673	TCCCTTGAGCCTGAG[A/G]GTTCGAGGCTGCAGT	84900
rs538024963	snp	C/T	1.65233e-05	0.00287426	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833847	TCCGATCCCTTGTCC[C/T]CATCCAGCTGTGGTA	84900
rs538058063	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764629	AAGGACAGTGGCTCA[C/T]GCCTATAATCCCAGC	84900
rs538060398	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740050	ATCTCTACTAAAAAT[A/G]CAAAAATTGGGTGGG	84900
rs538064467	snp	G/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737610	AGGAAGGAGGGGAGG[G/T]AGGAAGAAGGGAAGG	84900
rs538086436	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834470	TTGAGCGGATTCACA[A/G]TGTCACACAACCACC	84900
rs538162724	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848715	CACTCCTCACTGTCC[C/T]GCAAGTTTTACCCAA	84900
rs538164394	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769220	AAAAATTAGCTGGGC[A/G]TGGTAGCAGGTGCCT	84900
rs538187382	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800346	TACTAAAAATACAAA[A/T]AATTGGCCGGGCACA	84900
rs538199710	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760903	TAATTTTTAGAGACA[C/G]AGTCTTGCTCTGTTG	84900
rs538200821	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794056	GGATCACTTGAGCCT[A/G]GGAGTTCGAGACCAG	84900
rs538220030	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853694	CAACTGTCTTAGATC[A/G]AAGGAGAAGAAGCCC	84900
rs538237337	snp	C/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116844405	CCATGCCCAGCTGAT[C/T]TGTGTATTTTTAGTG	84900
rs538289216	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116753253	CATCCTGGGTTCAAG[C/T]AGTTCTTGTGCCTCA	84900
rs538378963	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116840030	ACAGGCTACAGGGAG[C/G]CAGGGAAAGGGCATT	84900
rs538392116	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802957	AAAATTAGCCTAGCA[C/T]GGTAGCATATGCATA	84900
rs538424059	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787333	CCAGCCATGGTGCCT[C/T]GAGCAAGTCGCTTAA	84900
rs538456281	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116841296	CATCTCTACAAAAAA[C/T]ACAAAAATTAGCCAA	84900
rs538488204	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792939	GGCCCTGACGTGTGA[C/G]GTTGGGTGAGCCACC	84900
rs538534039	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743136	GTGGTTGGGGTTATG[C/G]GCTCTGGATCACAAG	84900
rs538603076	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116748308	TCCTGCAGGCCTAAC[C/T]CCGGGCTCTCTGCTC	84900
rs538620718	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851200	CAACAGAGGCCTGGT[A/T]CAGTTTCAGAACCCA	84900
rs538621505	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741776	GCCTCAGCCTCCTGA[C/G]TAGCTGGGACTACAG	84900
rs538685255	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758131	TTGTTTTGTCTGATA[C/T]AAGAATAGCTACCCC	84900
rs538687287	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750383	GGTGGGGTGGGGGCT[C/T]CTCCTCTGAAGCCCA	84900
rs538748714	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116764411	ATAATAATCACCAGC[C/T]TCACTGACCCTTCTA	84900
rs538757637	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116850713	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	84900
rs538807469	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116784485	ATGTCAGCTGGTACG[A/G]AAAAACATGGCTGCC	84900
rs538813730	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116815687	TCATCACATCTGCAC[A/G]TGCACAAAATTCCTT	84900
rs538829163	snp	A/C	0.0143877	0.0835874	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737951	GGAACGCGGCAGGCC[A/C]GGGTCCCGGGCGGCA	84900
rs538844275	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777996	CGTGAGGATTAGTGA[A/G]ACACAGTGAGCAAAG	84900
rs538855122	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769903	AGCCAGGTGTGGTGG[C/T]AGGATCCTGTAATCC	84900
rs538860794	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809084	CTCTCCCCTGCCTAT[C/T]GCTGGTAATCCTGAG	84900
rs538873240	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759018	GTTTGGTCATTTAAC[A/G]TAATCCCAGACTTCT	84900
rs538874314	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841028	CAGATTCCCTATAAT[G/T]AGTAAGGGTTTTCAC	84900
rs538911046	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814126	TCATTGTCATGGCAA[C/T]ATTGTAGAAGCCAGT	84900
rs538921301	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116751149	TCAAATTCCTGGGCT[C/T]AAGCAATCCTCCCAC	84900
rs538930331	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116837773	AATAGTAACATATCA[A/G]CGTGGGTTTCTTAGC	84900
rs538956212	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777278	AGACAACATGAGTTA[A/G]GACATATAAAATATA	84900
rs538962646	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116843908	CCCCTACTCTGTACC[A/C]GCTCAGGGCTGGACA	84900
rs538967003	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791461	GGATTACAGGAGTGC[A/G/T]CCACCAGGCCTGGCT	84900
rs538997531	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116836102	GACCCCTTCCTCAGC[C/T]CACAGATCTCACAGT	84900
rs539005860	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789818	GTAAATGGAAGGAGA[A/G]TGGATGGGTGGATGG	84900
rs539011239	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746563	CTGACAGATGAGCGT[A/G]CATTACCTAGTTGGG	84900
rs539026454	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742241	TGAATCATGTTGGTG[C/G]GCTCTGGGGTACCGA	84900
rs539027821	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780509	CTCACCTCCTGCTGT[A/G]CGACCTGGTTCCTAA	84900
rs539035053	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116833094	CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGTTGG	84900
rs539042892	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786530	GGTTTGGGACAAGAT[A/G]AGGAAGGCATTTGAG	84900
rs539063339	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739448	AATGGCATTTATATT[C/T]TAATGGGGAGGACAA	84900
rs539072246	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828890	TCACATCTGTAGTCC[C/T]TACAGGGGACTCAGG	84900
rs539124039	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116797573	TTAAGTTAGAGTGAG[G/T]TCACTAGTGATGCAA	84900
rs539130715	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843217	TCCAAGGCCAGCTGG[C/G]CACAGTGGCTTGCAC	84900
rs539136564	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822870	GCCATGGTGGTGCAC[A/G]CCTATAATCCCAGCT	84900
rs539192755	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116822453	GCATTTTCCAGCTGC[A/G]TCACCTGGGGCAGGT	84900
rs539240943	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116774927	CTGAGTCAAACTGGT[A/G]CACAGAAAGAGAGAG	84900
rs539283046	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116767986	ATGGTTAGTGAACAC[A/T]GTATGAATAGTGCAG	84900
rs539310374	in-del	-/AG	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116802467	TTGAGGAATGATGAC[-/AG]AGACTCTGTGGCCCA	84900
rs539317382	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781023	CACTTTGTAAGAACT[A/G]TTGGTTGTGGGAAAT	84900
rs539332380	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736621	GTAAAAAGGAGAGCT[C/T]TTTATAACCATGTCA	84900
rs539334459	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821884	TGCATGGAGTGCATG[C/G]AGTGCAGTGGCGCAA	84900
rs539354126	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774298	TTAAGACGGTACCTT[C/T]TATGTTATGTGTGTT	84900
rs539395900	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773078	GTGATCCACCTGCCT[C/T]GGCTTCCCAAAGTGC	84900
rs539473892	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792444	GCTACCTCACTTCCT[C/T]CTCCTTGAAACGGAC	84900
rs539515311	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785168	GCTCCTTCTCTAATG[A/G]ATCCTTGAGGCGTCA	84900
rs539528068	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832546	CATACATGTGGACAT[A/T]TGTTTTCATTTCTCT	84900
rs539538850	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833719	TCATCACTGCCCGGG[G/T]CGGGGGGCCCCCCAG	84900
rs539550928	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817467	TTTTTGTAGTTTTTA[C/T]GTCTTCTTCCTTGCT	84900
rs539560004	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116821000	TCTGTGTTTGAGCTT[A/T]CTCATCTAAGAAATG	84900
rs539564563	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116851550	TCAAGACTAGCCTGG[C/T]CAACATGGCAAAACC	84900
rs539580032	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116812633	TCCACCTCCTGGGTT[A/T]AAACGGTTCTCCTGC	84900
rs539595524	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116751982	TTGCTGTGCCCTGGC[A/G]GGCTTATACACTGTT	84900
rs539605994	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819881	AAGAGTAGTCACACA[A/G]ACGATTTTAAATGTT	84900
rs539607595	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759816	TTTGGTGGTTTAATG[C/T]GCTATTTTTGTGCTG	84900
rs539626685	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853137	GTCTGATGAGGAGTG[C/T]TTCCAACACAGGCTA	84900
rs539628968	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116747559	TCTCATATAATAGAT[G/T]ATATGAGATCAAGTA	84900
rs539650931	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828226	GCTCTTATTCATCCA[C/T]TAAAGTAGTGCTTCT	84900
rs539693788	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752558	AGTAGATCTGGAAAA[A/G]TAGCTGGAGTACACA	84900
rs539727412	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811753	TCGTGGAAATCCAGG[A/C]CCTGTTGCAGGGGGC	84900
rs539832918	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116767759	GAATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT	84900
rs539839712	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116844563	TATGTCTCCGTTTCT[A/G]TTTCTAAATATTTCT	84900
rs539841596	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116812598	GGAGTTCAGTGGCGC[A/G]ATCTCAGCTCACTGC	84900
rs539843503	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811392	TTTTTTTTCCTTTTT[C/T]TGAGACAGAGTCTCA	84900
rs539847581	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116765787	TTGAGAATTAGGTAT[A/G]TAAGCTTGGATTTAA	84900
rs539854804	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791743	GCTGCTGTGAGCTTT[C/T]GCAGACAAGTATCTG	84900
rs539907850	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779028	AAAAGATCCACGTGA[G/T]GTCACACAGCAGGTT	84900
rs539957760	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761761	CTGGGTAGTTGAGCC[C/T]GTGCTCATTCCAGGT	84900
rs539998807	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116741213	TAGAGTCACACTGAT[A/G]GCCTCATACTAAACA	84900
rs540022580	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828020	TCAGCCAGATGCCAG[C/G]AGGCAGGGGCTCCCA	84900
rs540054718	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798506	GTAGTTTGCATCTCT[C/T]GCATTCATTTTCTCA	84900
rs540099094	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116741951	CCACTGCACCTGGCA[C/T]GGGTTAGGTTTCAAC	84900
rs540138862	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759015	TAGGTTTGGTCATTT[A/T]ACATAATCCCAGACT	84900
rs540164665	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797965	GCATACTGTTGGGCA[C/T]GGCTTATGGAAAGCT	84900
rs540216368	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762649	CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC	84900
rs540233062	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116833388	TCGCCTGTGATGCTC[A/G]AGTCAGCCCTCTAAA	84900
rs540251958	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755055	CTTGGTCATGAAATC[C/G]TTGCCTAAGCCAATG	84900
rs540257215	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116794372	GGAGGCCAAGGCAGG[C/T]GGATCCCTTGAGGTC	84900
rs540260544	snp	A/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116826371	GCAACAATTGCTACC[A/G]TTTCCCCTTCACGGT	84900
rs540297567	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116792367	GAAAATTTCTGAGAA[A/T]TAATTTTGGAGAAAA	84900
rs540298976	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768337	AACTCCTGACCTCAG[A/G]TGATCCGCCGGCCTT	84900
rs540310227	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116742431	TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT	84900
rs540318637	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116792611	ATTAATGTGCCAGGT[C/T]AGCGCGTAATCTAGC	84900
rs540367657	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799992	TGAGTGAGTTATTGC[C/T]ATATTAGTTCATGCA	84900
rs540374693	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840561	CCTCCTCGGAATGAA[G/T]GAATGGCTAAGCTGG	84900
rs540380223	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820131	AGTCTTACTGTGTCT[C/T]CCAGGCTGGAGTGTA	84900
rs540391411	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116835767	AGGTAGCAGGGGAAA[C/T]TCTTGATATTAGGCA	84900
rs540436127	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788994	TGGATGGGTAGATAA[A/G]TGAGAGGAGAGTAGA	84900
rs540458208	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116820901	ACTCATCACTAAACT[A/G]GAAGCCAGCCCTAGT	84900
rs540465208	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763244	TCTCAAAAGAAGATA[C/T]ACAAATGGCCAACAA	84900
rs540485256	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842147	ATTCCGTTCCTAATG[C/G]GCTGTGAAATTGGAG	84900
rs540486003	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116813484	CAGGTGTTTAGATAT[A/C]ATTTCCACTTGGAAG	84900
rs540514032	snp	G/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116819717	TTTCCATCCTGGCTC[G/T]CCCTTCTCTTGCCTT	84900
rs540516022	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826893	AGGGATGGATAGTAA[A/G]AATAATTTTTTAATA	84900
rs540576063	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116770525	ATGTAACAGCTTTTA[A/G]AAGTTATTTTAAGTA	84900
rs540577123	in-del	-/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116838015	ACACACACAAACATA[-/T]TTTTTTTAAAAAAAA	84900
rs540578850	in-del	-/GA			intron-variant	RNFT2	GRCh38.p7	12:116752208	AAAAAGAGAGAGAGA[-/GA]AAGCTTCGAGAGGAG	84900
rs540580382	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739302	CAAGGGATCTAGAAA[A/G]GGGGAACTGGGAGAC	84900
rs540593157	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746902	GGGAATTGGTTCCAA[C/G]ACCCCACGGATATGA	84900
rs540631742	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116784860	CACTCCAACCCCCTC[C/G]ACTTCATTCTTTTCC	84900
rs540669962	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116754175	TTCTTATGCCTTTGC[A/G]TCCTCATAGCTTAAC	84900
rs540683310	in-del	-/TTATG			intron-variant	RNFT2	GRCh38.p7	12:116774298	TTAAGACGGTACCTT[-/TTATG]TTATGTGTGTTTTAC	84900
rs540776956	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790890	TAAGCCTAATAAGGT[C/T]AAGGCTGCTGCAGTG	84900
rs540778794	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817506	AGGTGAGAGCATAAG[C/T]TGTATAACCTTGTCC	84900
rs540805930	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775291	AAAAGAGAGAGAGAA[G/T]AGCAACATAGCTGAG	84900
rs540831254	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116756492	GCTTTTATTACACTA[A/T]GGTATGTCCCTTGTA	84900
rs540929126	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116802277	TGACACATTTCCAAC[A/T]TATTAAGCATGGGAC	84900
rs540959783	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781643	CATCTCCTGATTCTC[A/G]CCCTCCTGCCTTCCT	84900
rs540960565	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116823300	GGGAGAGCAGCTTGC[C/T]CAAAGTCACACAGAT	84900
rs540965759	snp	C/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116774690	AGGCTACCCATAAAA[C/G]CAATTTGAGGACTCA	84900
rs540972595	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116812434	GCAGGTCCCTGGGGC[A/G]TGGCATTACTGAAAG	84900
rs540985881	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116743232	AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAACCG	84900
rs541006101	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769424	GGAGATTACAGCTCC[A/G]TGGGTGTTATTGCCC	84900
rs541006899	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784324	TCCTCTTACAATTCC[A/C]CAGTTCAGCTCTTGG	84900
rs541032608	in-del	-/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116784895	AGCGGAGCAGGACTC[-/T]TAAAAGAAAATTAAT	84900
rs541066391	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737656	GAAGGGGAGAAAGAA[A/G]GGAAGGGAAGGGGTA	84900
rs541079523	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776357	AGATCTTCATTTGAT[C/T]ATGATCATGGAAGCA	84900
rs541121450	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837174	CCTCCTCCTCCTCCT[A/G]ACATCAGGGACTAGG	84900
rs541130218	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116851371	ATCCCCAGCAGAGCC[C/T]GCACTCTTAACCTCC	84900
rs541134636	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820600	CCCTCTCTACCCCCA[C/T]AGCTTGTATCTTTTC	84900
rs541145162	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750634	CACCCTAGCTCTGTC[C/T]CCTCCTAGTTGTGTG	84900
rs541167436	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116776927	TGGGATTTTTTTTTT[C/T]TTTTTTTTGAGAAGG	84900
rs541201868	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809957	TGGGCTTGCAGACGT[A/G]AGCCACCGTGCCTAG	84900
rs541202362	in-del	-/CC			intron-variant	RNFT2	GRCh38.p7	12:116803803	ATGAGACCTCAGTCT[-/CC]ACTGGAACCTCAACA	84900
rs541342479	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116770972	CACCCATTTTTATTA[A/G]TAACATTTTGCTGAA	84900
rs541387596	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815086	TTAATTTTACACTGG[A/G]TATCATAAATGATGT	84900
rs541420932	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767189	TTTATTTAACCCAGT[A/G]TATCAAAAATATTTG	84900
rs541450710	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815844	GATTGATATGACTTC[A/G]GCAAAGTCACCCTCC	84900
rs541486979	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116834239	TCTCTTGCCTCAGCC[C/T]CCAGAATAGCTGGGA	84900
rs541494359	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772893	GAGTGCAGTGGCACA[A/G]TCTCAGCTCACTGTA	84900
rs541515067	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116769601	AGGATATAAAGAAAA[C/T]ATTTCTGTACAGCTG	84900
rs541565528	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116849203	AACGCGAGTGCAGGC[G/T]CCCCGAAGGCAGGGG	84900
rs541616464	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116843629	CTCCTTCTTCCTCCC[C/G]CTTCCTCTGTAGACG	84900
rs541674444	snp	A/G	0.000293686	0.0121143	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750073	CGGGGCGAGGGGGGC[A/G]CCTACCACCACCGCC	84900
rs541686460	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844496	CACCTTGGCCTCCCA[A/C]AGTGTTGGGATTACA	84900
rs541689881	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809414	AGCGCTTCTTTGAAG[C/T]CCGAGAAGATCCACA	84900
rs541696734	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849622	GACCTTCATCTTCCT[C/T]TCTCGTTCTGTGGTA	84900
rs541701464	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116747082	TATTTATTGAGAAAG[A/C]ATCTTGCTCTGTCAC	84900
rs541738166	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806968	AAAGTTCTTAAGTGT[C/T]CCTCTCCCTTTTTAC	84900
rs541740936	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760978	CCAACTCCCGGATTC[A/T]AGCAATCCTCTGACC	84900
rs541749164	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802355	GGCAAACTACAGGTG[A/G]GCCCACTGCTTGTTT	84900
rs541760216	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850246	TGCAACCTTGAACTC[C/T]TGGGCCCAAGCCATC	84900
rs541797987	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846224	TAATAGCTAATAGTT[A/G]TAGAGCACTTACTAT	84900
rs541799542	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799361	GGGACAGCCTGCTAA[A/C]CAACTAAAGGGTAAC	84900
rs541822478	snp	A/G	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116801736	ACCGTTTTTCAAACT[A/G]TGTTTCTGGGCCCTT	84900
rs541841338	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760267	AAACCTGCCCCAGAC[C/T]ATCCGCCTCCCAGCT	84900
rs541859273	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838725	TGAACATGATGTCAA[C/G]GTGAAAGTCTGACAA	84900
rs541864374	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812648	TAAACGGTTCTCCTG[C/T]CTCAGCCTCCTGAGT	84900
rs541885625	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116773341	CTAAGGGCCCTTTGG[G/T]TTACTAACTTAAGCA	84900
rs541892277	in-del	-/AT	0.0020668	0.03208	splice-acceptor-variant	RNFT2	GRCh38.p7	12:116836178	TCTCCCCTCCCTCAA[-/AT]AGAACTATGGAGTCC	84900
rs541938189	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818999	CATGGAGGTCCGGGT[G/T]CCTGCGCCACCCTTC	84900
rs541955499	in-del	-/AAAAAAAAA/AAAAAAAAAAAAAAAAAAA/CCACAAAAAAAAAAAAAAAAAAAAAAA	0.116138	0.211142	intron-variant	RNFT2	GRCh38.p7	12:116782079	CGAGACTCCGTCTCC[lengthTooLong]AAAAAAAAAAAAAAA	84900
rs541975771	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738558	TGCTCCTCTGAGTGC[A/G]TTTCGGTGCAGTCCT	84900
rs541983273	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851690	AAGTTGCAGTGAGCC[A/G]AGATTGCACCACAGC	84900
rs541994626	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116847277	AGATGTCTCCAGTTG[C/T]CTTCAAAGTGCCCTT	84900
rs541997972	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116805099	CTAGAGACACATTAT[C/T]AAGAAAGGGTTAAGA	84900
rs542022427	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116832688	CAGAAAGCTTCAGGG[A/G]CTTGTCCAAGGTCAA	84900
rs542070035	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116847018	GGTTCAAACGATTCT[C/G]CTGCCTTAGCCTTCC	84900
rs542084889	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116841414	GCCGAGATTGCACCA[A/C]TACACCATAGCCTGG	84900
rs542086679	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798886	CCAATCATAACAGTA[C/T]CTACATGTGTTAGTT	84900
rs542093487	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833524	CTGCCCAAAGGTGTA[A/G]GGTTTCTCCTACCCT	84900
rs542136753	snp	C/T	0.00795532	0.062565	intron-variant	RNFT2	GRCh38.p7	12:116745013	GCCCCTTGAGGATCA[C/T]AGCCATGGTGTTTGC	84900
rs542154404	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817432	TGGGATTACAGGCAT[A/G]AGCCACTGCACCAGC	84900
rs542155368	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116831720	GATTTTATCAGCTTT[A/G]TAGAAGCAGGATTTA	84900
rs542191144	in-del	-/A/AA/AAA	0.430285	0.173197	intron-variant	RNFT2	GRCh38.p7	12:116744225	GTGAGACTCCTCCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	84900
rs542199304	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751544	GAGTGACTGGGATTA[C/G]AGGCAACCGCCACCA	84900
rs542202290	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835050	AGATGGTGTTTTACC[A/G]TGTTGGCCAGGCTGG	84900
rs542202354	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842838	CTTGGCTTCCCAAAG[C/T]TTTGGAATTACAGGT	84900
rs542213262	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116800307	TCGAGACCAGCCTGA[-/C]CCAACATGGTGAAGC	84900
rs542216894	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748377	CCTGATTCCAACCCA[A/G]GAGGCCCTTGCTTGG	84900
rs542222242	in-del	-/TTC	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116804478	CAGCAATATGTAATA[-/TTC]TTTGGTTTATTCATC	84900
rs542259277	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851460	AAGCACACGAGAGGC[C/T]GGGTGTGGTGGCCCA	84900
rs542286137	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804431	GATCTTTATTAATAT[A/G]TGTAGCTCTAGTTCT	84900
rs542301086	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116846543	CATCCTCCTGCCTTC[A/G]CCTCCCAAAGTGCTG	84900
rs542309590	snp	G/T	0	0	intron-variant	RNFT2	GRCh38.p7	12:116765161	TACCTCCTTTGTCCT[G/T]CAGTTTCTGTCTTCC	84900
rs542318961	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848832	TGTTTTTTGTTTTTT[G/T]GTTTTTAGACAGATT	84900
rs542337741	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800656	AAAAATGGTTTAAAA[A/C/T]TGCAAAAAATTAGCT	84900
rs542381621	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116742468	GACAGGGTTTTGTTA[C/T]GTTTCCCAGGCTAGT	84900
rs542390654	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116794775	TAATATAGTAGCTAA[A/G]AAAACAAAACCAGGC	84900
rs542396135	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780068	ACAGCCATCTTTCAA[C/G]TTCAGAAAGCTGAGA	84900
rs542418415	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736814	AAGAAAAATGAAAGG[A/G]TGCAGTGTGTTGGAG	84900
rs542429386	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116821486	CATCCTAACAGGCCC[A/G]CAGGCCACCTTCCCA	84900
rs542439833	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777042	CCTGCCTCAGCCTTC[C/T]GAGTCGCTAAGACTA	84900
rs542470844	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818339	AAAAAAAAAAAAATC[C/G]GCTTTTTCGTCTGCA	84900
rs542480044	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116796210	CACCATGCCCAGCCT[C/T]TCCAGTGGTCATTTC	84900
rs542493973	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741992	ACACAAACATTGAGA[G/T]CATAGCTCTGAGAAA	84900
rs542501410	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792162	TCAAGCAATTCTCCT[C/G]ACTCAGCCTCCTGAG	84900
rs542512815	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831817	GTATCCCCCATCCCA[A/G]TCAAGATATAAAATA	84900
rs542522756	snp	C/G	0.000909504	0.0213055	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836315	GGGACCATTGGAGAC[C/G]AAGGCTGGGGGAGAG	84900
rs542559642	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116785615	AAAAGTCTGTTTGGC[A/C]CACCAGTGTATCTGT	84900
rs542610941	snp	C/T			intron-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116825056	GCTGGGGCTGGACTG[C/T]CCAAGATGGCATCTT	84900
rs542628026	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795326	GTCAGAAGAATCGCT[G/T]GAACCCAGGAGGCAG	84900
rs542642568	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116781794	TTAAGGTGTGGACAT[C/T]GGCTGGGCACGGTGG	84900
rs542663598	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788406	CTGCACCTACTGATT[A/C]ATCTGCCTCAAAGAG	84900
rs542672233	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794138	AGCATAGTGTCATGC[A/T]CCTGCAGTCCCAGCT	84900
rs542704527	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831085	CAACTTGGGGCCAGG[C/T]GCAATGGCTCATGCC	84900
rs542730184	snp	C/T	0.00030839	0.0124137	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849427	GGACGGCGCCACGTC[C/T]GCACACTTCCAGGTG	84900
rs542749710	in-del	-/AAAG			intron-variant	RNFT2	GRCh38.p7	12:116827232	CTCAAAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA	84900
rs542765784	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763290	CTCAGCATCACTACC[A/G]ATCAGGGAAATGCAA	84900
rs542768193	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807812	TTTCTTGAGTCTGTG[C/T]TTTTGTTTTGAGATA	84900
rs542808139	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116782046	ATCGCACCACTGCAC[A/T]CCAGCTTGGGCGACA	84900
rs542831637	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808201	AACTCCTGACCTCAG[C/G]TGATCCACCTGCCTT	84900
rs542840556	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822136	CACCCTGCCTGGCCA[A/G]CCTCCTTCAACCAGA	84900
rs542843432	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116834627	TCTCTATGAATATAC[A/T]TATTATGAATGTTTC	84900
rs542861459	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116776980	TGGAGTACAGTGGCA[C/T]GATCTCGGCTCACTG	84900
rs542902694	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116789159	GGAGAGTGAGTAGAT[A/G]GATAGATGGGTGGAT	84900
rs542926642	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775348	AGTCACCAGTCTAGA[C/T]GGTGCTTGTATGTGA	84900
rs542988446	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782912	CCTTTGTAAATAGCA[C/T]AGGTATTAAACTCTT	84900
rs543000735	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116740175	GCCAAGATCGCACCA[C/T]TCCGTCTTAAAAAAA	84900
rs543084054	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116824514	CCAGCCCACTGCTTC[A/G]CCAGCTCTAGGGTGT	84900
rs543145519	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116834069	TATTTTAATTGAGGG[A/G]AAATTCATACGACAT	84900
rs543152892	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781382	AGGCAGAGGTATTTA[C/T]TCCCCCAGCATGTTA	84900
rs543160024	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784709	CCTCTTTCTTCCTTG[C/T]TTCTTCCAGTCAGCA	84900
rs543170825	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811510	TCTCCTGAGCAGCTG[C/G]GATTACAGGCGCCCA	84900
rs543238783	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761924	TAGTGCATCCAGGCC[A/G]GTCGCGGTGGCTCAC	84900
rs543259393	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116753310	CACATGCCACCATGT[A/G]TGGCTAATTTTTGTA	84900
rs543275673	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762751	TGAGTAGCTGAGATT[A/G]CAGGTGCATGCCACC	84900
rs543282874	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779949	GGTATCACCTGTAGG[A/T]CATAGTGATTGCCAG	84900
rs543297744	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820820	GGGCAAATAATTTCA[A/G]TGTCCATCTCCTGGG	84900
rs543317939	snp	A/C	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116776048	ACTCTCAAAAAAAAA[A/C]CAAAAAAACTCGTAA	84900
rs543351114	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116768432	ATTACAGTCATGTGT[C/T]ACGTAATGATGTTTC	84900
rs543375899	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116823530	CTCTACTAAAAATAT[A/G]AAAATGAGCTGGGCG	84900
rs543384792	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830091	GATAATTTTAGACTT[A/G]AAGAAAAGTTGCAAA	84900
rs543408182	snp	C/T	0	0	upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738040	CAGCCCAGTCTGCTC[C/T]CGGCAGCCTTGGGCG	84900
rs543411530	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764022	ATTCTACTCAGCCAT[A/G]AAAAGGAATGAATTA	84900
rs543431009	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811929	GGGTCCTGGGGCTGC[C/T]TGGTTTGAATCCTGC	84900
rs543437189	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116817594	ACAGAGGACACTACT[A/G]ATTGGGAAACCAGAA	84900
rs543444221	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764689	CTGAGTTCAGCAGTT[C/T]GAGACCAGCTTGGCC	84900
rs543446109	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770714	AGGCGCATGTTACCA[C/T]GCTCAGCTAAATTTT	84900
rs543449844	snp	A/T	0.242488	0.249887	intron-variant	RNFT2	GRCh38.p7	12:116850336	ATTTTTTTTTTTTTT[A/T]AATTTTTAGTAGAGG	84900
rs543517179	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116824697	CTCTTCCTGGCTTGC[A/C]GAAGGTTGTCTTCTC	84900
rs543522188	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737712	GAGGAAGGTAACGAA[A/G]GAAGGAAGGAGAAAG	84900
rs543629681	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116791060	TGTACAACCACCACC[C/T]CTGTCTAGTTCCAAG	84900
rs543633599	snp	C/T	0.000134021	0.00818491	intron-variant	RNFT2	GRCh38.p7	12:116851844	GTTACCCCTTGGTCT[C/T]CTGTCTTTATGTCTT	84900
rs543639074	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845372	AGGGGTTTTCACCAG[A/G]AAGAATGGCATAGGA	84900
rs543669044	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116833502	GGGTGACCCACTCTC[A/C]AGCCCTCTGCCCAAA	84900
rs543676546	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116759284	TCATATTTTGGAATT[C/T]GTTGCACTGGGCTTT	84900
rs543716990	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843689	GTCCACAGCCGTGAA[A/C]TCCTCAGCTGGGCCC	84900
rs543750818	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116765247	ATTAAACTGGAATCT[A/C]TTATTCATTGGAGTA	84900
rs543926608	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116822188	CCCCTTAGTTCTGAT[G/T]ACACCGTCAGTCACA	84900
rs543943649	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774528	TCAGAGCTGTCAGAA[C/T]TGAGGGAAGATTCTT	84900
rs543955215	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750726	TGATTTTATAGTCTT[C/T]ATGGGATCACAGTGA	84900
rs543966349	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812740	GGTTTTACCATGTTG[A/G]CCAGGCTGGTCTCTA	84900
rs543982313	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767702	CTCCTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAT	84900
rs544035643	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743406	CGAGTAGTTGGGACC[A/G]TAGGCACGCACCACC	84900
rs544074520	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116803177	GTCCATCTCATGAGC[A/G]ACATTCACAACAGCA	84900
rs544079155	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116830099	TAGACTTAAAGAAAA[G/T]TTGCAAAAGTAATGC	84900
rs544116038	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116740315	AAGGTATCGCAGGGA[C/T]TGTTCATCCAGGTGT	84900
rs544136009	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848277	TTGATTCCATGTCTT[C/T]GCTATTGTGAATAGT	84900
rs544168195	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801373	GGAAGATTCTAGAGC[A/G]TGTAGCAAGAAAAGC	84900
rs544186256	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807001	GGCTTCCCGGAAATG[A/G]CTCCCGTCACTTTCA	84900
rs544193522	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116768223	CTCCTGTCTCAGCCT[C/T]TTGAGTAGCTGGGAT	84900
rs544209341	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794313	GGTTTAAAACCAGGC[C/T]AGGGCTGGGCATAGT	84900
rs544246356	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116799503	TTTTGCTGGGTGCCC[A/G]CCGCACTATCTCAGA	84900
rs544263144	snp	A/G	0.0111196	0.0737302	intron-variant	RNFT2	GRCh38.p7	12:116839464	ATGGATGGATGGATG[A/G]ATGGAAGTGAATGAT	84900
rs544282827	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116805870	ATGAGGTTCACCCAG[C/G]ATATCAAGGAAAATC	84900
rs544297744	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116792550	AATGCCTCCCTGGCA[A/T]CTGTCCAGCTCCCTT	84900
rs544320668	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116746035	TGAGCTCCGGAGTTC[A/G]AGACCAGCTTGGCCA	84900
rs544321658	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838843	TCAGACAAGACACCC[A/G]TTGTCCCAGATCTAG	84900
rs544342362	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116782284	AGCACTTTGGGAGGC[C/T]GAGGCAGGAAGATTG	84900
rs544374814	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826291	GAATCCGCCTTCCCA[A/G]CTTGACACTCCCACC	84900
rs544380348	snp	C/T	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116842082	GGTCCTCTCCTGGCT[C/T]AACTTGGGGAGGAGC	84900
rs544413699	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116794571	CCACTGCACTCCAGC[C/G]TGGGTGACAGAGTGA	84900
rs544443735	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748293	TTCTGGGCTCTCCAT[C/T]CCTGCAGGCCTAACT	84900
rs544501538	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799944	CACAGGGGTGAATCT[C/T]ATGTGAATGGCGTGG	84900
rs544510270	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825879	GAATCCCAAATCCCA[C/T]GCCTTTAAACCACTA	84900
rs544510875	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819624	CCGGGTGGTGACGTC[A/G]CCGGCAGCACCCGTT	84900
rs544577265	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752695	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT	84900
rs544599231	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807866	CGGTGTGCTTTGATG[C/T]GATTGTGGCTCACTA	84900
rs544641424	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742041	GACATTGAAAGATGA[A/G]ATTTTTATTTCTTCC	84900
rs544651379	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116829252	TGGCCATACACTAAG[G/T]TGCTGTCCATTGGTC	84900
rs544685226	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116798090	ACGGGCCCTGGTCCA[A/G]TAGGACTGGTGTCCT	84900
rs544688028	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116802229	GCTCTGAGAAGTCCC[A/G]CAATAAAGAAATTCA	84900
rs544715730	snp	G/T	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116752137	GGAGGATTGCTTGAG[G/T]CTGGGAGTTCGAGAC	84900
rs544740809	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760069	CAGGTCACTGGTGTT[G/T]TGTACCAAGGAGGAT	84900
rs544767749	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795435	AAAAGAAAGAAGAAA[G/T]AAAATGAATTCCCCT	84900
rs544769526	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773674	AGAGGCCCTAAATGC[A/G]ACTACTTGGAAGAAT	84900
rs544803448	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789327	AGAGTGGATGGATGG[A/T]TGGGTAAATGGAAAG	84900
rs544805754	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116834874	TTTTTTTTTTAGACC[A/G]AGTCTCGCTCTGTTG	84900
rs544897627	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760810	ATGCGAGCTGCCGCC[C/T]GCTGCTCTCTCTGGA	84900
rs544912422	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822175	CCCTCCTCTCTGTCC[C/G]CTTAGTTCTGATGAC	84900
rs544966161	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786649	ACAATTCACTGTCAC[C/T]TCTTTCTGGATGAAA	84900
rs544973180	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836430	CTGGGTTCCAATCTC[A/G]CCTCTGCCTCTTAGT	84900
rs544980178	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776301	AAGATAAAATGGAAA[G/T]GATAAGGCAGATCTT	84900
rs544982619	snp	C/G/T	0.00037458	0.013681	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749970	CCTCCCCACCAGCTC[C/G/T]TTCCCCTCCAGCCTG	84900
rs545006069	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116790263	GAGGCAATGTGTTAA[A/G]CAATGCCATTTGTTC	84900
rs545047454	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820881	ACTAAGTGTTCAACC[A/G]AGAAACTCATCACTA	84900
rs545055224	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781901	GGGCTACACGGTGAA[A/T]CCCCGTCTCTACTAA	84900
rs545092245	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116804939	ACCACTGCACTCCAT[C/G]CTGGGTGATGAAGTG	84900
rs545117386	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796001	GAAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC	84900
rs545138627	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116749338	GCTGGAGTGCAGTGG[C/T]GAGATCTTGGCTCAC	84900
rs545149025	snp	A/C	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116756833	GGTATTAGGGTGATG[A/C]TGGCTTCATAGAATG	84900
rs545219872	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801563	GACTTAACTCATAAC[A/G]CTGTTGTGAGAATTA	84900
rs545226667	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116809680	CAGAAAGACCTTTTC[-/T]TTTTTTTTTGAGATG	84900
rs545263003	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776721	TTCTATGCTGAGTGT[A/T]CTTCTCCCTGCTTTG	84900
rs545264518	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736851	AATTCTACCAATCAA[C/G]TTATGCACAAAAAGC	84900
rs545279652	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116783592	CCTCACTTGAGCAAT[A/T]ACACCCCTCCCTGTG	84900
rs545342084	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769004	CCAAAGTGCTGAGAT[G/T]GCAGGCGTGAGCCAC	84900
rs545362059	snp	A/T	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116785714	ACTGAAGTTAGCTCA[A/T]TCCTGCCCTGTGCCT	84900
rs545362856	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753765	TATAAAGTATCCCCA[C/T]AGGGACCTAAATCCT	84900
rs545375722	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772669	GGACCAAAAACACCT[C/G]CAATTCTGTCACCTA	84900
rs545392136	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116749547	TGACTCCCAAAGTAC[A/G]GGGATTACAGGCATG	84900
rs545399456	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818784	CCTCTCCGAGCCTTG[C/T]GTTCTCATCTGTAAA	84900
rs545399493	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116792576	CCCTTTTTTTGATGA[C/T]GATTATTTTATTCGG	84900
rs545421558	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821316	CCACCCCTCCTGGCC[A/G]GGCGCTGCTGTGAAG	84900
rs545532635	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785551	CCTGTTTCAGCCTTC[A/C]AAAGTACTTGTGTAA	84900
rs545535285	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796093	TTTGTATTTTTAGTA[A/G]AGAAGGGTTTTCACC	84900
rs545567513	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738499	GCTCGCGACGTTGTT[C/T]CCGAAGTGCACCTGC	84900
rs545573133	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116763564	ACAAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	84900
rs545599295	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116849510	CCGGACCCAGCCCTG[C/T]GGGGGCTTCCTGAGA	84900
rs545656000	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773335	TATCAACTAAGGGCC[C/G]TTTGGGTTACTAACT	84900
rs545685789	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769359	CGTCTTAAAGTTAAC[C/T]GTAAGGCAGCCTTAG	84900
rs545690951	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116805357	GTAGAATATATGTAC[A/G]TAGATTTATTTTAAG	84900
rs545768728	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818279	AGTGAGCTGAGATCG[C/T]ACCACTGCACTCCAG	84900
rs545772526	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851403	CACTGCTCTGCCCCT[C/T]AGACATTCCAGGCAT	84900
rs545780248	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767163	AGGTGGAATCAATTA[C/T]AATAATTGATTTTAT	84900
rs545782808	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757769	CTTGGAGAAAGTTCC[A/G]TGCGCTGTTGAATAG	84900
rs545820102	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116750797	ACTATATGTGTGTGT[A/G]TATATATATATAATA	84900
rs545832171	in-del	-/AT	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116819815	TGGATTTTTACAAAC[-/AT]ATGTAATCACTCAGA	84900
rs545838850	in-del	-/TT	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739332	CCCATAGATGTTTTA[-/TT]CATTGAGTAAATACT	84900
rs545840231	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116767728	GGGATTACAGACATG[C/T]GCCACCACGCCCAGC	84900
rs545843435	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116826987	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	84900
rs545849996	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818913	AGAGCAAGGAGGAAC[A/T]GGGGTAAAGGTGCAG	84900
rs545890294	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739357	AAATACTTGTTGAGC[A/G]CCACTCTGTGCCAAA	84900
rs545999310	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846971	TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	84900
rs546020368	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839607	GGATGGACAGATGGA[C/T]GGATGGATGGAATGG	84900
rs546024114	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116840223	ACTCCTGTTGATTTC[C/G]TGCTTACAAGTTCTT	84900
rs546037385	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744988	CTTTGAAGTGCAGAA[A/G]AAGCTCAAGGCCCCT	84900
rs546055339	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815518	CTGGTCCCCTTCTCT[A/G]TCTTCAAAGTGCATC	84900
rs546062562	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847505	CCCATTGGTCTTTCC[A/C]ATCTCCCTGCCTTTC	84900
rs546102542	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751442	GAGTTTTGCTCTTGT[C/T]GCCCAGGCTGGAGTG	84900
rs546139562	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852503	ACAATCCCACTTGCC[A/T]GAATAATCAAGTGGG	84900
rs546180451	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803261	GTGCAACCGACACCA[C/T]CTGCCACGGGGGTGA	84900
rs546184644	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747340	GGATTATAGGCGTGA[A/G]CCACCATGGCTGGTC	84900
rs546221078	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796975	TGGCACCATTGGAGG[A/G]GGTGTGCTACTGGTA	84900
rs546221638	snp	A/G	0.0115144	0.0749975	intron-variant	RNFT2	GRCh38.p7	12:116765840	GAATGGTCAGTCCAG[A/G]GCAGCGGGCCAGAGG	84900
rs546242692	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116770760	GATGAGGTTTCTCCA[C/T]GTTGCCCAGGCTGGT	84900
rs546304546	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840985	GTAATGTCATTTTTC[A/G]TAATTAAATGCTTCA	84900
rs546374065	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775625	TGGAACCAAGTCCAC[A/C]TTCTTCCCTTATCTG	84900
rs546386706	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830692	AAGTAGGTGGATCAC[C/T]TGTGGTCAGGAATAT	84900
rs546391680	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784772	CGTGGGAGCCCATCC[C/T]CCTTCTATATCTCCA	84900
rs546446804	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116798326	ATTCTATATACAGCT[C/T]CCACGTTGCTTTTAT	84900
rs546509330	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797523	TGATGCCACTGCACT[A/C]CAGCCTGTCTATCTC	84900
rs546511083	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740392	GCATCCCTCTGGAGA[C/T]GAAGAGGAGGGGGAG	84900
rs546534484	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746381	ATTATAATATATGGC[C/T]AGGATTGAGAGCCAC	84900
rs546537183	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761908	AAAGGATTGAATGAA[A/G]TAGTGCATCCAGGCC	84900
rs546538303	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781533	AAGTTTTGGCAGGGC[C/T]GTGTTCTTCCTCCGT	84900
rs546575893	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116786406	ATGAGCCACCGCGCC[C/T]GGCCGAGATCGGGTA	84900
rs546614383	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834256	CAGAATAGCTGGGAC[G/T]ACAGGCATCCACCAC	84900
rs546656611	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116826619	AATTGCTACCTTTAA[C/T]GGGGTGCCACATAGG	84900
rs546754147	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116793561	CCTCTCCGACATCAT[C/G]ACCCATGACTCTGTC	84900
rs546770783	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116777892	CCTTTATGCTTATGT[A/C]GTGTGACTTTGGGCA	84900
rs546802040	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738788	TACAAGCATCCGAAA[A/G]TAGAGTTTCGAGCAT	84900
rs546853780	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810441	AGACTCTAAGCTCCA[C/T]GGGGGCAGAATAAGA	84900
rs546905413	in-del	-/T	0.444133	0.157519	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738387	AAAAAGAGAACGCGA[-/T]TTTTTTTTTCTTTTC	84900
rs546921568	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819897	ACGATTTTAAATGTT[A/C]TAGTAGTCACGTTAA	84900
rs546955783	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815443	CCTTTGGGAGGCTCC[A/G]GGGGACAATCCATTT	84900
rs546965776	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812303	GAGTGATGACCATAG[C/T]AGCCCGACATAAATA	84900
rs546994533	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116767858	GCTGGGATTACAGGC[A/G]TGAGCCACTGCCCCT	84900
rs547032630	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773049	GGCCAGGATGGTCTC[A/G]ATCTCTTGACCTTGT	84900
rs547184975	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807119	AGCAAAGATTGAGAC[A/G]CTTATTTTGAAAGAG	84900
rs547189771	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844065	TCAGGGGGTCTGTGA[A/G]GTCAAAACCATTTAT	84900
rs547227182	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116766661	CGCTTGGGTATCAGT[A/G]GAATAGAAAGGTGCC	84900
rs547230234	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116799087	TTCTGGAGACAAGTC[A/T]ACTTCCAGGCTCATT	84900
rs547274250	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851072	TCACAACAGCCCTGT[A/G]ATGGGGGAGGTACTG	84900
rs547290513	snp	A/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116803489	TTCCTTTTAGAGAAA[A/T]AAAAGCCACTCCGCT	84900
rs547426462	snp	A/G	0.00755907	0.0610114	intron-variant	RNFT2	GRCh38.p7	12:116850235	TCACAGCTCACTGCA[A/G]CCTTGAACTCCTGGG	84900
rs547458104	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768542	TGCAGCCATCATAAC[A/G]CTGTAGCACAGTGCC	84900
rs547470018	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754572	TCTCACACTGTTTTT[C/G]ATAGCGGTTGTACTA	84900
rs547489194	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736377	TGAGGTGGCAGAAAA[C/T]ACAAGTCACAGAAGT	84900
rs547527080	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769086	AAAAGTTGGCCGGGC[A/G]CAGTGGCTCACACCT	84900
rs547565101	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807914	GCTCAAACGATCCTC[C/T]CACCTCAGCCCCCTG	84900
rs547582998	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762246	TTAGCCAGCCATGGT[G/T]GCTCACACCTGTAAT	84900
rs547609895	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116744042	GACCAGCCTGGCCAA[C/T]ATGCTGAAACCCCAT	84900
rs547637430	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769960	GAATCATTTGAACCC[A/G]GGAGGCAGAGGCTAC	84900
rs547641343	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845523	ACCCAGCTGGTCAAG[A/G]TGGAGAAAGGGCATC	84900
rs547661978	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809641	GGGCTTCACCCCTGC[C/T]CTCTTTTTCACAGAC	84900
rs547697035	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116782537	GCCTCTTAAAAAAAA[A/T]AAAATAAAAAATGTA	84900
rs547706074	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850584	CTGCAGATTAGAATC[C/T]CTGTGAGCCCTGTGA	84900
rs547719822	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788686	ATCAGTATCTGCTGT[A/G]TATCCAGAAGTGTTC	84900
rs547719964	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116795473	AGATCCGGGAACTGC[A/G]CTGTCTAATATAGTA	84900
rs547722292	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808372	TGGAATTACAGGTGC[A/G]AGCCGCTGCATCCAG	84900
rs547736498	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743820	TGCAGGGAAGAACAC[A/G]GGGCTCAGCCAAACC	84900
rs547789131	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835360	TGTTAAATTGCACAC[C/T]CTCAACTCCTCAAAT	84900
rs547796933	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813111	CAGGCATGTGCCACC[A/G]TGCCTGGCTAATTTT	84900
rs547850850	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116765550	GTCTGAAAAAAGGCA[C/T]GAGCTGTTGAGAATC	84900
rs547873264	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116741297	TGATAGGTGAGCCAC[C/T]TGACTCATTGTATCA	84900
rs547873685	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759748	CATGGATACCAGTGC[C/T]TGTTGCCATGGAGGT	84900
rs547896459	in-del	-/GAAGGTAA	0.498813	0.0243321	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737544	GAGGAGGAAGGTGAG[-/GAAGGTAA]GGAAGGAAGGGAGGC	84900
rs547901225	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814438	GTAGGGAGAAGGTAA[C/T]ATTCATGCAAAGCCT	84900
rs547923534	in-del	-/TGGAGTGCA	0.0489382	0.148574	intron-variant	RNFT2	GRCh38.p7	12:116821864	CTCTGTCGCCCAGGC[-/TGGAGTGCA]TGGAGTGCATGGAGT	84900
rs548003487	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786402	AGGCATGAGCCACCG[C/T]GCCCGGCCGAGATCG	84900
rs548009215	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828634	GTAGGTGTCCAGAAA[G/T]GGAAGCAAGGATGGG	84900
rs548037701	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755459	TTGGCTCTCACAAAG[C/T]GTGCTTCTCTGGGTG	84900
rs548042455	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742147	AAGGACCGAGGAAAA[A/G]GCATAGGCCACAGCC	84900
rs548060988	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842490	GTCTGTTTGCTGTTA[C/T]GAGACTGGGGTGCAA	84900
rs548065874	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116833045	CGCTTGAGTAGCCTC[C/T]GAGTAGCTGGGATTA	84900
rs548111874	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792637	CTAGCCTGTAGAAAG[A/T]GATGTGAATAGTCTT	84900
rs548115040	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116748802	AGTGTGCTGGTTACT[A/G]AAGTGGGCTCTAGAG	84900
rs548122937	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842992	TCACGCTGAACACCA[A/C]GTGCTAGGTCCAGAA	84900
rs548134413	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116743565	GAGCCACTGCACCCA[A/G]CCTAGAATTTATATC	84900
rs548207328	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819610	ATTAATGGCTGCCGC[C/G]GGGTGGTGACGTCAC	84900
rs548221010	snp	A/G/T	3.51953e-05	0.00419484	upstream-variant-2KB, missense, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737832	GACGAGCGACAGCCC[A/G/T]AAGACCAGGGCGAGC	84900
rs548233102	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851612	GGGCGCGGTGGCGGG[C/T]GCCTGTAATCCCAGC	84900
rs548261107	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804744	GGGAGGCCACAGTGG[A/G]CAGATGACCCCTAGG	84900
rs548293344	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116742823	TATGGTGGTGCATAC[A/C]TATAGTCTCAGCACT	84900
rs548299405	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837535	ATTTTTGTTGCTGTT[G/T]TTATTGCTGTTTGGA	84900
rs548301539	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737164	CTCTGCCCTGGCCTA[C/G]CAACCCCTTCCCGCT	84900
rs548351539	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116825422	TAAGGCAGCAGTAAC[A/G]TAATGGCCACATTTC	84900
rs548358666	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738874	CCCCAAGGATTTGCA[A/G]TGTGGGATAATGGAG	84900
rs548385805	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780408	ATGTGCAGTTCACAA[C/T]ACGGTTCCCACTCCT	84900
rs548402971	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116767196	AACCCAGTATATCAA[A/C]AATATTTGTTTTTTG	84900
rs548412849	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116750986	GCTCACTGCAACCTT[C/T]GCTTACTGCAACTTT	84900
rs548413149	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816362	GAAGATTTTTACTCA[C/T]AGCCCAGCAACTCTT	84900
rs548426611	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116797055	GACAGCCCTCTACTG[C/T]AACCCAGAGTTATCC	84900
rs548528214	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116839859	CAATATGTCACTCCC[A/G]CTCCACCCACTACCC	84900
rs548540603	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116845272	AAATATATATATATA[G/T]ATAGAGAGAGAGAGA	84900
rs548560179	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784926	CTGATTGTCCTCTCC[G/T]ATCACTTCCCCTCAC	84900
rs548590939	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116840359	ACTTGCCTGAGGTCC[C/T]GTTGTTCCTCAGTCA	84900
rs548604087	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823805	TAACATTTATTGAGC[A/G]CTTACCATGCGCCAG	84900
rs548630309	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833729	CCGGGGCGGGGGGCC[C/T]CCCAGCTGGGTCCTT	84900
rs548651365	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779609	CACAGCTACCCTTGA[C/T]GCAATTTTCATCCAC	84900
rs548685563	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739913	TACAATACCTTAAGA[A/G]TTTCAAAGAGGGCCG	84900
rs548691984	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834414	ATGAGCCACCACGCC[C/T]GGCCTCCAGTAACTA	84900
rs548723150	in-del	-/GGCTTGCACCTGTA	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116843224	CCAGCTGGGCACAGT[-/GGCTTGCACCTGTA]ATCCCAGCATTTTGG	84900
rs548723827	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116781951	GGGCGTGGCAGCATG[C/T]GCCTGTAGTCCTACT	84900
rs548733297	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791273	CCGTGCTATGTTTTC[A/G]AGGTTCATCCATGTT	84900
rs548747150	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820514	TCCGGCATCTGGAAA[G/T]TTCCTGTGTCCTCAC	84900
rs548760469	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116791456	AGCTGGGATTACAGG[A/G]GTGCGCCACCAGGCC	84900
rs548820189	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116778832	TCCAGCCTGGGAGAC[A/G]GAGCAAGACTCCATC	84900
rs548829939	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116811120	AGTTATCCACCAGGC[A/G]TGATGGCTCACGCTA	84900
rs548904435	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116777764	CCATGAGGAAGGGAA[A/C]AATTCCCATTTTATT	84900
rs548913787	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768753	TTTTTTTTTTTGAAA[C/T]GAGTTTTGCCCTTGT	84900
rs548965571	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775722	ATTGGACATATATCA[C/T]AATTAATATGATTCT	84900
rs548979341	in-del	-/TC/TCTTTC/TCTTTTTC/TCTTTTTCTTTTTC			intron-variant	RNFT2	GRCh38.p7	12:116850625	TTTTCTTTTCTTTTT[lengthTooLong]TTTTTTTTTTTTGTT	84900
rs548988747	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116825971	TGTATAAATATTATT[C/G]ATCTTGATACAGAAA	84900
rs548999361	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812904	TGTCCATAATCCCAC[A/G]CCATTCAGAGGCAAG	84900
rs549073158	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116819226	TGTCCAAATAAGAGA[C/G]CGGGGAGTGGACGCG	84900
rs549084030	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747997	GGAGTTCAATACCAG[A/C]CTGGCCAACGCGGTG	84900
rs549094923	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787271	GAGATCATCTGCCAG[A/G]TCGGCCAGGTGCTAG	84900
rs549106363	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798213	CCTGGGAAACAGAAC[A/G]AGACTCTGTCTCAAA	84900
rs549131709	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787700	CCTGGGCAATAGAGG[C/G]ACATGTTGTCTCTAA	84900
rs549165764	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780826	CCAGGTCGGCACCAC[A/G]CACTTGACACTGGAA	84900
rs549168525	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814615	GCAGGGCAACTTCAT[A/G]GGCAAGCACCCTTTG	84900
rs549258311	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782290	TTGGGAGGCTGAGGC[A/G]GGAAGATTGCTTGAG	84900
rs549267597	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116799669	AGCTGGGCACGATGG[C/T]TCATGCCTGTAATCC	84900
rs549294920	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116781260	CCTCCATCTTTCTCA[C/G]CCTGCTCTCTGCCCA	84900
rs549304999	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776383	AAGCACTGGAGATTT[A/G]GCAGAGTGTGGAAAT	84900
rs549336719	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809658	TCTTTTTCACAGACC[A/G]GTAGACCCAGAAAGA	84900
rs549340016	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774771	AGAATGTCAAGGTCC[A/G]GGTGGAGGGTGGAGG	84900
rs549362388	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852974	CTGTTAACACTGTAA[A/G]GAATGTAACATGTGG	84900
rs549378004	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853540	GGTCCTGGAATCTTT[C/T]AGGACTTCTGCTGTA	84900
rs549385825	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116767525	GCCGCACCTGGCCCC[A/G]AAAGATTGTCATTTC	84900
rs549397926	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837806	TGACAAATGTACCAC[A/G]GTAATGCAAGATGAT	84900
rs549406645	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807212	CTATAAATGAGAGAC[C/T]GGAAGCTCAGCAAGG	84900
rs549426573	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746778	ATATTTGTACCTGTC[C/T]AGAGGGTTCCTCTGA	84900
rs549445160	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848011	CCTCCCCCAGCCCCC[A/G]CAACAGGCCCCAGTA	84900
rs549481819	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816876	AAAAAGTAGAGAACT[G/T]CTAGTTTCTTAGAAA	84900
rs549524043	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804549	TTTTTTTACCATTAT[G/T]TATATTACAGTAATG	84900
rs549552130	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848390	CTCAACCTAGAAGGC[A/G]GAGGGATCGCTTTAA	84900
rs549561173	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837610	TTTTAAATGGATAAT[A/G]TATTTGCATGAATCA	84900
rs549587042	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754391	CACCCGTTGATTGGT[C/G]GGCATTTGGGTTGGT	84900
rs549612128	in-del	-/A	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116838021	ACAAACATATTTTTT[-/A]TAAAAAAAAACATAA	84900
rs549616941	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822916	GCACGAGAATCACTT[A/G]AACCCAGGAGGCAGA	84900
rs549670579	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116760636	GGTGAGTGTTCGGGA[A/G]AGGAGGGTCTCCCTT	84900
rs549688166	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116833075	ACAGGTGCGCCACCA[A/C]GCTCAGCTAATTTTT	84900
rs549688813	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748824	GCTCTAGAGAGAGTC[A/G]GCCTGGGTTCGAATC	84900
rs549704627	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845604	AAGGTCATGTGGCAC[A/G]TCAATGACATCAGTT	84900
rs549709353	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761164	TTTTGTTTTTTTCTT[C/T]TTGAGACGGAATCTT	84900
rs549761560	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756354	CTATTGTAAAAGGGG[C/T]TGAGTTCTTGATGTG	84900
rs549801245	in-del	-/ATT			intron-variant	RNFT2	GRCh38.p7	12:116846901	ACTAGCATGCCCAGG[-/ATT]TTTTTTTTTTTTTTT	84900
rs549874370	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116763654	TGTGGTGGCAGACGC[C/T]TGTAGTCCCAGCTAC	84900
rs549874839	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795032	TGTCCCAGAAACATA[C/T]ATAGAAATATATCAT	84900
rs549885154	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116811432	CCAGGCTGGAGTGCA[A/G]TGGGGCCATCTCGGC	84900
rs549895642	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770471	GTCCCAGTCATTAAG[C/T]GATGTATGACTGTAT	84900
rs549896458	in-del	-/T	0.0387552	0.1337	intron-variant	RNFT2	GRCh38.p7	12:116756306	GGTATATTCCTAAGG[-/T]TTTTTTTTTGTTTTT	84900
rs549914285	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116797218	CAAAATATGTGTGTT[A/G]GAGTCCAAACCCCAG	84900
rs549951165	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791448	CCAAGAGTAGCTGGG[A/C]TTACAGGAGTGCGCC	84900
rs549952008	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116851755	GTCTAAAAAAAAAAA[A/G]AAAGAAAGAAGGGAG	84900
rs549978676	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783932	TCCCAAGTACTTTAC[A/C]TGTACAAACTCATTG	84900
rs549980977	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769557	GTTGTAACAAAAAAT[G/T]TTAAAAATAGGAAAA	84900
rs549990041	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116837202	AGGTGTCAATTCAGC[A/C]AATGTGTATTGGGGT	84900
rs550001691	snp	G/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116800931	TCACTGCTGGAAGGT[G/T]ACAAAGTAGGACTCA	84900
rs550016079	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755507	AGTTGAACCCAGGTA[C/T]CTTTCTCTTCCGCTT	84900
rs550019316	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851138	CACAGAGCTTGGTGC[A/G]GTAACTTTCCCAGGG	84900
rs550040483	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842623	CTGTCACCCAGGCTA[A/G]AGTGCAGTGGCATGG	84900
rs550055486	snp	C/T	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116789722	TAAATGGGAGAAGAG[C/T]AGATGGATGGATGGA	84900
rs550073432	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764782	CTGTAATCCCAGCCA[C/T]TTGGGAGGCTGAGGC	84900
rs550080863	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116750891	TATATTATATATATA[-/T]ATATATATATATATA	84900
rs550090460	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783133	CCCGGTAGGAGATAC[A/G]CACTCTTATACCCAT	84900
rs550090662	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790516	GCAGTAACAAACTTA[C/T]AGCAGCGGGAGCAGC	84900
rs550094110	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116821739	AAATGCAGATTCCTG[A/G]CCCTGTGCTAGCTTG	84900
rs550122857	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777207	ACAGTCGTGAGCCAC[C/T]GTGCCCAGCCTCAAA	84900
rs550160000	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753026	GTGGAAGAAAATTCA[A/G]TTCCGTTCTGCCATC	84900
rs550184783	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116749533	GATCTTCCCACCTCT[A/G]ACTCCCAAAGTACAG	84900
rs550200382	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116796268	AAGGTCAGGTATCTC[A/G]TTGCTGGGTGGTTAC	84900
rs550217295	snp	C/T	4.94271e-05	0.00497102	utr-variant-3-prime, missense	RNFT2	GRCh38.p7	12:116852690	TGGAGCTGGAGAAGA[C/T]TGATGAAAGTGCAGG	84900
rs550225182	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116759797	CTCCGTGAGGGTTCT[C/T]AGCTTTGGTGGTTTA	84900
rs550229046	snp	A/G	6.87782e-05	0.00586382	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750115	CATTTCCACCATGGC[A/G]GCCACCGCGGGGGCT	84900
rs550230458	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116770662	TCCCAGCCTCAAGCA[A/G]TCTTCCCACCTCAGA	84900
rs550262081	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116752510	CTCATTCTTGTTTTA[C/T]GTGCTTATAGTGAAG	84900
rs550262379	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760383	TTCTTACCCTGTTCA[A/T]ATTGTTACACAGTTC	84900
rs550267271	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116798056	TCTGGAGTCAAGTCC[C/T]GCCTGCTACCTCACT	84900
rs550267517	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798968	CATTTATGAGTTCAC[A/G]GTTCTGTAGGTCAGC	84900
rs550293067	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809221	CATTCATTCATTCAT[C/T]CATCACCTGGGAGCA	84900
rs550301879	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116840303	GTAGTTACCCTATTT[A/G]ATAGAGACAAAGAAT	84900
rs550310087	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792731	CCCGAATCCTCATCA[A/G]TCCTTGTCTGTGGAG	84900
rs550350405	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736463	TCAGCCTCTCTGTTT[A/G]CCTAAGGTGGCAGGT	84900
rs550379179	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829505	AAAATCAGGCAGGGG[A/G]TGAGTGATGATTGGA	84900
rs550380460	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781502	TCCAAAGTGGGTTTT[A/G]CTGCGGTGAAAACAG	84900
rs550422418	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847054	GCTGGGACTATAGGC[A/G]TGTGCCACCATGCCT	84900
rs550452335	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116786411	CCACCGCGCCCGGCC[A/G]AGATCGGGTAGTTCT	84900
rs550466314	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742179	TTATTGTGTTTTCTG[A/G]GGGAAAGAAAGGCAA	84900
rs550514059	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738244	CTAGCGCCGGACCCG[G/T]CGACGCCAAGAAACC	84900
rs550514893	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828744	AAAAGGCAGGAAGGG[A/G]GGGAAGGAAGAAAGG	84900
rs550518146	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116754133	AGGCACAGTCTTCCC[A/G]GCAAGTCTCCAGAGT	84900
rs550542679	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831920	GATTGCTTGAGCCCA[C/G]GAGTTTGAGACCAGC	84900
rs550549550	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819865	TGTCCGACAGAAATA[C/T]AAGAGTAGTCACACA	84900
rs550614609	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739391	TGTCCTGGATGCTGA[A/G]GCAGAGGGGTGATCC	84900
rs550618435	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830396	GGGCTCAAGCAATTC[A/T]CCCACCTCAGCCTCT	84900
rs550620304	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116838393	TTCACACACACATGA[A/G]CTCTTGGTAGGATAA	84900
rs550664990	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116786226	TCCCAGGTTCAAGGT[A/T]TTCTCCTGCCTCAGC	84900
rs550702562	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739670	CCTGAGGCAGGGACA[C/T]GCTGACACATTAGAG	84900
rs550706798	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736805	CTCACATGGAAGAAA[A/G]ATGAAAGGGTGCAGT	84900
rs550729480	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116784200	ATTCACTTCTGTAAG[C/T]AGACTCAGAGATGAG	84900
rs550742606	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116825019	CACCGGGTACAGCTT[A/G]TCTCTCCTCCCCATG	84900
rs550852056	snp	A/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116833084	CCACCACGCTCAGCT[A/T]ATTTTTGTATTTTTA	84900
rs550864726	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747203	CTGGGACTACAGGTG[C/T]GTGCCACCATGCCTG	84900
rs550886664	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761309	ACACACCACCACGCC[C/T]AGCTAATTTTGTATT	84900
rs550915041	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833630	CGCGTCTCCCTGGCC[A/G]TATCGCAGCCCCATT	84900
rs550927130	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116821078	CTGGCCCCTGGTAAG[C/G]GCTTAATACGGGGGT	84900
rs550928814	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828604	TCCAGAACCTGGCAT[C/T]GTGTCTGGTGCATAG	84900
rs551002100	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116818408	GTAACAGGCCCTGGC[C/T]CAGTGCCTGGTTCAG	84900
rs551010481	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831678	TATTTTTACAGATAT[A/G]GATGCTTGGGGCAGT	84900
rs551011249	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116785727	CAATCCTGCCCTGTG[C/T]CTTCTGGTTTATTTT	84900
rs551011316	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779666	CATGTTAGCATGCCC[C/T]GGGACCTGCTTCTCC	84900
rs551065721	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828123	TGCCCACCAAGATGG[C/T]GCTCAGACCAGTGAC	84900
rs551076732	in-del	-/GTTA	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116801609	GTCAAGTGCTGGCTG[-/GTTA]GTTAATTATTGTCAT	84900
rs551123587	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785082	CGCCTTGGTTCCCCC[C/T]CTGTTTCTTCCCTCT	84900
rs551128858	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736299	GGACGGAGTCCTGGC[A/G]CACCCCACCACTCAG	84900
rs551207096	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772138	GCTCTGTTGCCCTAG[C/G/T]TGGAAGGTAGTGGTG	84900
rs551213006	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116835363	TAAATTGCACACCCT[C/G]AACTCCTCAAATTAG	84900
rs551232454	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812203	AACAAGACAGAGGGA[A/G]ATGGCACCTGGAACA	84900
rs551323198	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809618	GTCTCTCTGGTTCCT[C/T]AAAGACTGGGCTTCA	84900
rs551327055	in-del	-/AA	0.0689305	0.172377	intron-variant	RNFT2	GRCh38.p7	12:116800859	AAAATAAAATAAAAT[-/AA]AAACCATTTAACAGA	84900
rs551395773	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807869	TGTGCTTTGATGCGA[C/T]TGTGGCTCACTACAG	84900
rs551446081	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788596	ATTGTTTGTTTAAAT[A/G]TCTGCCTTCTCTGCT	84900
rs551468869	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808233	GCCTCCTAAAGTGCT[C/T]GTAAGCCACCACACC	84900
rs551486637	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775476	GCGACACTTACCACT[A/G]AGCTTGAATCTTCTC	84900
rs551513372	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758282	TCTATTCTGTGATTC[C/T]GTGTCTTTTAAGTGG	84900
rs551528166	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782379	AAAAATTTAAAAAAT[C/T]AGCTGAGTGTGGTGA	84900
rs551530210	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116806024	ATTAAACTAAACATA[C/T]AGTCCCCCTTTAAAC	84900
rs551538934	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834534	ACCCTGAAAAGAAAT[A/G]CCCATTAAGCAGTCA	84900
rs551593977	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116813018	TGGAGTGCAGTGGCA[C/T]GATCACGATTCATTG	84900
rs551657400	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777109	TTTTAGTAGAGACAG[G/T]GTTTCACCATGTTGG	84900
rs551670697	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748067	TGATGGCAGGTGCCT[A/G]TAGTCCCAGCTACTC	84900
rs551686572	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787777	GAGTTATCACCTAGA[A/G]AGGAGGCAGGTGAGG	84900
rs551729626	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768514	GCTAGAAAATTCTAT[C/T]ACCTAGTGATATTGC	84900
rs551768120	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804671	TCCAGAATCCCAAGA[C/T]GGTTCTTTCTCGAGG	84900
rs551805901	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116841576	AACATGGTGAAGCCC[A/G]GTCTCTACTAAAAAT	84900
rs551896329	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116771878	CTTTTGAAACGAGAC[A/G]CTTCCTCCACAAATC	84900
rs551907573	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116740658	CAGAGGGGTTACTGA[-/T]TTGTCTAGGGTCACA	84900
rs551930747	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842384	AATGGAAATCTGCCT[C/G]TCACATGCCCGAGGT	84900
rs551992636	snp	A/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116755374	AGAGGTCTTTTTTTT[A/T]TTTTTTTTTAACACC	84900
rs552029550	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116748455	GATAACAGTTCCCAC[A/G]TATTGAGAACCTATT	84900
rs552053443	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797843	TTAAGGGGCAGTTTA[C/T]GCAGAAATTTCCAGG	84900
rs552068541	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116762194	GACCAGCCTGAACAA[C/T]GTGGTGAAACCCCGT	84900
rs552087543	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792270	GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAG	84900
rs552103395	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754419	GGTTCCACAATTTTA[A/G]AATTGTGAATTGTGC	84900
rs552129369	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758187	TGAAATGCCTTTTTC[C/T]ACCCCTTTAAGTTTA	84900
rs552206690	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850544	GGAGGAGCCTAGAGA[C/T]CACTGCCTCCCAGAT	84900
rs552218057	snp	C/T	0.0236746	0.106192	intron-variant	RNFT2	GRCh38.p7	12:116782798	CCTATCACAGGCAGC[C/T]CCTCCAGACAGCTTT	84900
rs552245723	in-del	-/T	0.0444908	0.142359	intron-variant	RNFT2	GRCh38.p7	12:116764352	AACCTATGGAAATAA[-/T]TTTTTTTTTTAAAGT	84900
rs552250388	in-del	-/TGGAGTGCA	0.172304	0.23762	intron-variant	RNFT2	GRCh38.p7	12:116821872	CCAGGCTGGAGTGCA[-/TGGAGTGCA]TGGAGTGCATGGAGT	84900
rs552255742	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749679	CCCTATCTTTAAACA[A/G]GGTCACATTCTGAGG	84900
rs552324080	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831360	GGGTTCAGGATGTCA[A/G]AATGACTTCTCACTG	84900
rs552327769	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851221	TCAGAACCCACATCT[A/G]AAAAAAAATAAATTT	84900
rs552360487	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116755757	TTCCCTTGATGTCTA[C/T]GATATCACCTTTCTT	84900
rs552367706	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778702	TAAAAATACAAAAAA[G/T]TAGCCAGCTGAGTTG	84900
rs552371230	snp	A/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116785212	TTCTAGATCCCCCTA[A/T]GTCCAGTTCTTTCAT	84900
rs552381469	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738302	AGTCACATGCTGCCC[A/G]GGCTGCGCGGGTGAT	84900
rs552408202	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116836934	GACTACATCTCAAAG[-/A]AAAAAAAAAGGACAT	84900
rs552413927	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816553	CAGCTCTGGTTTTAA[C/T]AGTGAGTGTCCAGTT	84900
rs552419305	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790243	TATTGCTGAGCATTT[A/G]TTATGAGGCAATGTG	84900
rs552436454	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745375	AGAGGGTTTTTTGCC[A/G]TATTGGCCAGGCTGG	84900
rs552465124	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116847094	TTGTATTTTTAGTAG[A/T]GACGGGATTTCACCA	84900
rs552482873	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116812972	TTTTGTTTTTTTCTT[C/T]TGAAACAGGGTCTCA	84900
rs552541385	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790686	ATTAGGCTGGGCTCA[A/G]TGGCTCATGCCTGTT	84900
rs552568874	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773386	CCTTTAGGCATTGTT[C/G]CATGCAGGGACTCAA	84900
rs552569096	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796409	CCCTTCCATATCCTG[A/G]ATCATCTTAACTAAG	84900
rs552620254	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745903	GTGGAGCTCTGTCCA[A/G]AGCTATGGTTTGCAG	84900
rs552620697	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116784401	TAGGTCAGCAGCTGG[C/T]CAATGAATGGGCTGC	84900
rs552656480	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843914	CTCTGTACCAGCTCA[G/T]GGCTGGACAGTAGGA	84900
rs552732839	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768020	TGGAATATTTCTGGA[A/C]GGACAACCAAGAAAC	84900
rs552768563	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116822986	TGGGCGATAGTGCGA[G/T]ACTCTGTCTCAAAAA	84900
rs552809890	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774303	ACGGTACCTTTTATG[C/T]TATGTGTGTTTTACC	84900
rs552824863	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783984	AACAGGGTCCTGTTA[C/T]TACCACCATCCCATT	84900
rs552829185	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780526	GACCTGGTTCCTAAC[A/G]GGCCACAGTCTAGTA	84900
rs552858180	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806798	AGCATTTGATTTTTC[C/T]CCTTTCATCTGTTGC	84900
rs552874127	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116760966	TCATTGTAGCCTCCA[A/G]CTCCCGGATTCAAGC	84900
rs552896144	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767596	GTTTTTTCTTGTTTT[C/T]TGAGACAGAGTCTCA	84900
rs552928404	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739467	TGGGGAGGACAAATC[A/G]TAAATAAATAAGCAA	84900
rs552949503	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851666	GAACTGCTTGAACTC[A/G]GGAGGTGAAAGTTGC	84900
rs552957203	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781026	TTTGTAAGAACTATT[G/T]GTTGTGGGAAATACA	84900
rs552981162	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826204	CTTCTGGAGCCAGCC[C/T]TCTGTTGTTTCGATG	84900
rs552983457	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818916	GCAAGGAGGAACTGG[A/G]GTAAAGGTGCAGAGG	84900
rs553000455	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832637	TAGACACTACAGAGT[A/G]GGTGTATTTTCATCT	84900
rs553031566	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853175	TCCCCTATACCAGTG[C/T]GAAAGCAGCCAGGAG	84900
rs553036622	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116759706	GCACAGAGTCCTGTG[A/T]TGTGAACTGTCTATG	84900
rs553046346	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819541	GGTGATCTCATCCGG[A/G]CCCGGGGGAGGAGGA	84900
rs553055773	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818043	GAAACGGGAAAGGGC[C/T]TTCTCTGTGGGATGG	84900
rs553076504	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765797	GGTATATAAGCTTGG[A/C]TTTAATTCTACACTG	84900
rs553118299	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825753	TATCTATATGTATGT[A/G]TGTATGTATGTGTGT	84900
rs553121638	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116805028	TACAAGTTGTTTTTT[C/T]TTGTTTTCCTTTAAG	84900
rs553133314	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116744989	TTTGAAGTGCAGAAA[A/C]AGCTCAAGGCCCCTT	84900
rs553161358	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807394	AAATATCCAGTGTCC[A/C]TAGTACTGGTCTAAA	84900
rs553183621	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838027	CATATTTTTTTAAAA[A/G]AAAACATAAGTTATA	84900
rs553215035	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846181	AATAAACTGTAAACA[C/G]ATAAGATAATAATCA	84900
rs553279248	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839345	AGGAAGGATGGATGG[A/G]ATGGTTGGATGGAAT	84900
rs553295037	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751990	CCCTGGCGGGCTTAT[A/G]CACTGTTGTTTTAGT	84900
rs553316621	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840542	GCCAGGCCTGTGCAC[A/G]TTGCCTCCTCGGAAT	84900
rs553320614	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809566	TTCACTGGGAGCCAT[A/G]CCAAGATGGTCAGTT	84900
rs553361248	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116759035	AATCCCAGACTTCTT[A/G]GAGGCTTTGTTCATA	84900
rs553405417	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820714	ACTCTGGAAAATCAG[A/G]CTGGATTTAAATCCC	84900
rs553454573	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814797	GATTCTCATGCTTCA[A/G]CCTCCCGAGTAGCTG	84900
rs553462846	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771562	ATTTTTTTGTAATGG[A/G]CACTTTTTTTTACAT	84900
rs553463252	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779798	TAGTGATGTCTGCCA[C/T]AGACCCTGCAGTGGG	84900
rs553466599	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817856	TATGACAGGCACTGC[A/G]AAGGTGTTGGGGATA	84900
rs553469715	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848130	TGTTAGTTTGCTGAG[A/G]ATAATGGCTTCCAGC	84900
rs553478138	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116765076	TTTGCCTGTATGTGC[A/G]TATCTTCCATAAGAG	84900
rs553551023	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116772293	ATTTCTAATTTCAAA[A/G]GTAATTTTTATTTTA	84900
rs553577309	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798507	TAGTTTGCATCTCTC[A/G]CATTCATTTTCTCAT	84900
rs553577399	snp	C/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116792132	TTGGCTCACAGCAAC[C/G]TCCACCTCCCAGGTT	84900
rs553581123	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742337	CAGTGGCACGATCTC[A/G]GCTCACTGCAGCCTC	84900
rs553614536	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792461	TCCTTGAAACGGACA[C/G]TGCTAGGGCCGAGGA	84900
rs553616697	snp	A/G	0.00993419	0.0697739	intron-variant	RNFT2	GRCh38.p7	12:116825761	TGTATGTGTGTATGT[A/G]TGTGTGTATTCAACC	84900
rs553621202	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116805631	AGGTGTGAGCCGCCA[C/G]ACTGGCTAATTTTTA	84900
rs553631938	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116762679	CTGCCTCCCAAGTAG[C/T]GAGATTACAGGTGTG	84900
rs553656812	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116771202	GCGTTGGCTCACGCT[C/G]TAATCCCAGCACTTT	84900
rs553659179	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749060	TATTAATATTATTTG[C/T]ATTAGTTCCTAGGAC	84900
rs553685703	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843314	CCTGGCCAACATAGC[A/G]AGACCCCAACTCTAC	84900
rs553696682	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808756	TTTTTAATGGCAAAC[A/G]GCAGGGAGGAGGGGC	84900
rs553717852	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116744815	GAGTCTTCCCTGGTT[A/G]TACTGGAGGCCCCTG	84900
rs553722480	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794116	TAAAAAACTAAAAAC[A/G]TATCCAAGCATAGTG	84900
rs553756695	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850000	AGGCACCCACCAACA[C/T]ACTTGGCTAATTTTT	84900
rs553784556	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116795761	TCTCTACAAGTCCCC[G/T]GTTCAGGGAGACAGC	84900
rs553791495	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756576	CTTTTTCTGCATCTA[C/T]TGAAATGATCATGTG	84900
rs553860453	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768891	GCTCACCACTACGCC[C/T]GGCTAATTTTTGTAT	84900
rs553864780	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116776590	TTGTCAGTAATTTTG[C/T]CCTACTCAAAATAAC	84900
rs553920818	in-del	-/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116823752	ACCAGACTTAATTTA[-/T]TTTTTTCATATTTCC	84900
rs553945719	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753402	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	84900
rs553965860	in-del	-/TTC			intron-variant	RNFT2	GRCh38.p7	12:116786052	GCCAGCCTCTCAGTA[-/TTC]TTCTGACATAGGTGC	84900
rs553979168	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795756	AGAACTCTCTACAAG[C/T]CCCCTGTTCAGGGAG	84900
rs554001103	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791655	CATTGTGTGGATAGA[C/T]TACAATTTGTTTAGC	84900
rs554006499	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755841	TAGAGAACATATATC[C/G]GGTGCCTCTCCTCTT	84900
rs554018097	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789917	GATGGATGGTAGATG[A/G]ATGGATGGGAGGAGA	84900
rs554108806	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763381	AAAAATAATAGATGT[C/T]GGCATGAATGCGGGA	84900
rs554114330	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791613	CCATGCCCGGCTTTC[A/G]TTCCTTCTTATGGCT	84900
rs554134751	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838991	AGGTAAATGGGTCAT[A/G]CTGATTCCTAAAAGC	84900
rs554149503	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791894	CCCAGCGGAAGAAAA[C/T]GAAAACAGCCAGAGG	84900
rs554151437	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784652	GCACCTCCCTCCACC[C/T]CACTGTTCACATCAA	84900
rs554165086	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781735	TTAATCACATCAGCA[A/G]AGTCTCTTTTGCCAC	84900
rs554203374	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747760	TTAGTGGTCTGTGGA[A/G]GTGCCTGCAGGGTGA	84900
rs554238475	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116740140	AATCGCTTGAACCTG[C/G]GAGGCAGAGGTTGCA	84900
rs554253798	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116844436	GAGACAGGCTTTCGC[C/T]ATGTTGGCCAGGCTG	84900
rs554337776	snp	A/G	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116795564	AGTTGCACCAACCAC[A/G]TTTCAAGGGCTCAAA	84900
rs554338887	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758253	GCAGCAGATGGTTGG[A/T]TGGTGAGTTCTTATC	84900
rs554344339	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841385	CTGAGCCCAAGAGGC[A/G]GAGGCTGCAGTGAGC	84900
rs554375890	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116751357	AGTGCTCAGCCTCCT[A/G]TCTGACACATACTCA	84900
rs554390347	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811498	CTTGTGCCTCAGTCT[A/C]CTGAGCAGCTGGGAT	84900
rs554407129	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834658	ATATAAATGGAATCA[C/T]GTAATAGGTGCCCTT	84900
rs554442264	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787898	GTTTTTTGTGCTCCA[A/G]ACAGACAGACCCTAC	84900
rs554485164	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116782047	TCGCACCACTGCACT[A/C]CAGCTTGGGCGACAG	84900
rs554498862	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737506	AAAGGGAAGGGGGAG[A/G]AAGGAAAGGGGGAGG	84900
rs554524136	snp	A/C	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116740940	TAGGGGTCTAAGATA[A/C]GACTAGTGCAGGTTT	84900
rs554548555	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830636	AGGGCTGGGCGCGGT[C/T]GCTCACACCTGTAAT	84900
rs554568192	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116770009	CACTGCATCCAGTCT[G/T]GGTGATAGAATGAGA	84900
rs554592316	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116795265	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCATGT	84900
rs554604120	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116838468	ACAGTTATTGCTAAA[C/T]TGCCCTCTGTAAAGA	84900
rs554621786	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750641	GCTCTGTCCCCTCCT[A/G]GTTGTGTGATGCTAG	84900
rs554650908	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822544	GCCTCATAGTGGTGT[A/G]CACAGAGTGGTGCCT	84900
rs554665866	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116786445	AGTCATGCAGCTGCT[C/T]GGTGGTGGGGTCAGG	84900
rs554729108	snp	C/G	0.0263992	0.111815	intron-variant	RNFT2	GRCh38.p7	12:116752808	ACTTGAACCCAGGAG[C/G]TGGAGGTTGCAGTGA	84900
rs554729698	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116764879	CCTGGGCAACAAGAG[C/T]GAAAGTCCGTCTCAA	84900
rs554736611	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749216	TGGCTTGTGGACAGC[C/G]GTCTTCTCCCTGGGT	84900
rs554741486	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116837947	AAAAAATCTTTGAAA[A/G]ATATAAAAAGGAGGC	84900
rs554741951	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786160	GAGTTTCACTTTTGT[C/T]CCCCAGGCTGGAGTG	84900
rs554798026	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784121	CCCTGAGTCTGAGCT[A/C]TTAATCTGTCTGCTG	84900
rs554805786	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823410	AAAATCAGGCCAAGC[A/G]TGGTAGCTCACACCT	84900
rs554841961	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116768799	GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT	84900
rs554844733	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779117	CAGGTGATACTTAGA[A/C]GGCTCCTGAGTGAGT	84900
rs554873938	snp	A/T	0.0205511	0.0992634	intron-variant	RNFT2	GRCh38.p7	12:116851234	CTAAAAAAAAATAAA[A/T]TTATTAGAGATGAGG	84900
rs554958572	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767654	GCACGATCTCAGCTC[A/G]CTGCAATCTCCGCCT	84900
rs554987149	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815857	TCGGCAAAGTCACCC[C/T]CCCAGCAGGACAGAT	84900
rs555008618	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116829003	ACACAATGTTTTAAG[C/T]GGAAAAAAAAAAAAC	84900
rs555057698	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116798914	GTTTTCATTTACTGC[A/C]TAACAAATGACCACT	84900
rs555064435	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736756	TTGGGTAAGATTTCC[C/G]CACCCGTGCTCCTTG	84900
rs555078717	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116777468	AAGTACAGAAACTGA[A/G]CATGAGGTTTCACAT	84900
rs555113673	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803025	TCTTGAGCCTGGGAG[A/G]CAGAGGATGCAGTGA	84900
rs555119379	in-del	-/TCTCT/TCTT	0.178465	0.239547	intron-variant	RNFT2	GRCh38.p7	12:116768736	TTATTTTTCTCTCTC[-/TCTCT/TCTT]TTTTTTTTTTTTGAA	84900
rs555122067	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116822034	GAGACGGGATTTCAC[C/T]GTGTTGGCCAGGCTG	84900
rs555125560	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826263	TCATCTTGGCAGTGA[A/G]GAAGTCGGAATAGAA	84900
rs555127096	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762467	AAGTACTGGGTATGG[G/T]GGCCTATGCCTGTAA	84900
rs555162035	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781098	GAGTGATTCACAATA[C/T]CTGTGTTGTCTAATC	84900
rs555171295	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116810445	TCTAAGCTCCATGGG[A/G]GCAGAATAAGAATCT	84900
rs555195000	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819594	CGCCGCCAGGAGGGG[A/G]ATTAATGGCTGCCGC	84900
rs555202481	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768176	TGCAATCCCGGCTCA[C/G]TGCAACCTATGCCTC	84900
rs555209991	snp	A/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116844508	CCAAAGTGTTGGGAT[A/T]ACAGGCGTGAGCTAC	84900
rs555258246	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754121	AAGCCACAAGCCAGG[C/T]ACAGTCTTCCCGGCA	84900
rs555324166	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116819995	TATTATTTCAACATG[C/T]AATCAACATAAAATT	84900
rs555325450	snp	C/T	0.00251219	0.0353523	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833929	CCTGATCGTTCTCTA[C/T]AGCCTCTGCAAGGTG	84900
rs555333483	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801423	CAGCCCTGTGGAATC[A/G]TCGAAAGAGCACATA	84900
rs555355617	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116853994	GACTTCCTGCACTTC[A/C]GACTCTCCCCTAAGA	84900
rs555388062	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812668	GCCTCCTGAGTAGCT[A/G]CGATTACAGCATGCG	84900
rs555419208	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848188	ATCTCGTTCCTTTTT[A/G]TGGCTGCATAGTATT	84900
rs555442691	in-del	-/GGAA	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116839760	GGTGAATGGATAGGT[-/GGAA]GGAAGGAAGGAAGGG	84900
rs555464406	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826744	CTGTAGGAAGTTGAC[C/T]TGAGTAATAAGGATG	84900
rs555464694	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116800583	AGGTTGCAGTGAGCC[A/G]AGATAATGCCACTGC	84900
rs555486373	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846795	CTAAACCAGTTAAGA[A/G]TAAGTGGTAGACATT	84900
rs555521176	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798596	TTATATTTTTGAGAC[A/G]GAGTCTCTGTCACCC	84900
rs555531192	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739146	AACTGAAGTCAGACA[A/C]CATCTGACTGATATA	84900
rs555535345	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833139	GGCCAGGCTGGTCTT[C/G]AACTCCTGACCTTAA	84900
rs555541708	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116777510	GATAGGTTTACACTA[C/T]TCAGCTGTAGAGTAT	84900
rs555573307	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116807999	TTTTAAGACAGTTTC[A/G]CTCTTGTTGCCCAGG	84900
rs555599728	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116767363	AGCTGGTACTACAAG[C/T]GCATGCCACCACACC	84900
rs555608137	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116841442	TGGGTGACAGAGGGA[A/G]ACCCTGTCTCAAAAA	84900
rs555612644	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839445	TGGATGGATGGATGG[A/G]TGGATGGATGGATGG	84900
rs555671966	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832789	CCTCAAAGCAACCCC[A/G]TAAGGTGGGAATTCT	84900
rs555674013	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840435	CCCATTCCACAAGGC[C/T]TGGTCTCAGGCTTTG	84900
rs555707894	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116807452	TCTCACAACAATCCT[A/G]TGAGGTAGACACTCT	84900
rs555781117	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116771457	AAAATGAGATCCTAT[C/T]GTTAAAAAAAAAAAA	84900
rs555786716	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746024	GGTGGATCACTTGAG[C/T]TCCGGAGTTCGAGAC	84900
rs555792165	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116773128	CACCACGCCCGGCCA[A/C]TTTTTCATAATTTTA	84900
rs555837871	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116805189	CTCCATCACTTCCTC[A/T]ATCGCCCACTGCTTG	84900
rs555936323	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829814	TTGAACTCCTGGCCT[C/T]AAGAGATCTGTCCAC	84900
rs555938416	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736830	TGCAGTGTGTTGGAG[A/G]GGTGGAATTCTACCA	84900
rs555963315	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786054	CAGCCTCTCAGTATT[A/C]TTCTGACATAGGTGC	84900
rs555966691	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737563	GTAAGGAAGGAAGGG[A/C]GGCAGGGAGAGGGGA	84900
rs555997237	snp	A/G	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116847398	ATTAATCTTCCAATG[A/G]GGGGGTTCTATCCCC	84900
rs556044499	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773211	AGGTGATCTGCCCGC[C/T]TTGGCCTCCCAAAGT	84900
rs556047166	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830324	ACAGGGTCTTACTCT[A/G]TCACCCAGGCTGGAG	84900
rs556051680	in-del	-/GT	0.00597247	0.0543191	intron-variant	RNFT2	GRCh38.p7	12:116747583	TCAAGTATGAAAACA[-/GT]GGAAAATTTCCACCA	84900
rs556051742	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790785	AACATGGTGAAACCC[A/T]GTCTCCACCAAAATA	84900
rs556056131	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829151	GGGCAGCTGAGGGTG[G/T]GTGGTTCAGGGAATG	84900
rs556072473	snp	A/C	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116836935	ACTACATCTCAAAGA[A/C]AAAAAAAAGGACATA	84900
rs556108477	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116804301	TGTTAGAAATGTAAA[C/G]CCTCAGACCCCACCC	84900
rs556117945	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843454	GCCTTAATCACACCA[C/T]TGCACTCCAGCCCAG	84900
rs556144367	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788738	ATACATGTGTGTTTG[A/G]GTGGGTAGATGGATG	84900
rs556165068	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795903	TCATCTCTCCAGTGG[C/T]CATTTCTTTTTCTTT	84900
rs556255432	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850091	CTCAAATGATCAGCT[C/T]GCCTCAGCCTCACGA	84900
rs556278700	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116827810	TTGGGATTTGGCCCA[A/G]AAACCAGCCTGCAGC	84900
rs556330974	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755958	TACCATGCTGTTTTG[A/G]TGACTATGGCCTTAT	84900
rs556391856	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116828622	GTCTGGTGCATAGTA[A/G]GTGTCCAGAAATGGA	84900
rs556397786	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784296	GTAGGCAGCATCCGC[A/C]GCACGTGTCGTGTCC	84900
rs556430555	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782665	CATGGGTCAATGCTA[G/T]TCCTTGTACTTCACA	84900
rs556452301	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116798469	ACCCTCTGCCATTTA[A/C]CAGCTTTGGGACCTT	84900
rs556539456	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820846	CTGGGATTGTCAGAG[G/T]CTGGGGACAGCCTGC	84900
rs556540354	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779972	ATTGCCAGTGGCTCT[G/T]TAAGGTGACCCAAAG	84900
rs556595082	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754772	CATGTTTGTTGGCCA[C/T]TTGTATATCTTCTTT	84900
rs556600913	snp	A/G	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116794542	GGGGGAGGCTGCAGT[A/G]AGCCGAGATTGTGCC	84900
rs556623688	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116764957	TCTCAAATGCAGTAA[C/T]ATCCAAATGGCACCT	84900
rs556664795	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842051	CAGGCTGCAGTCAAG[C/G]TATTACCAGGGCTGT	84900
rs556683636	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738443	TGCCCTTGCAGTCCC[A/G]GAGCGTTTTGCGCTG	84900
rs556737102	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838534	ACAGCCGCTTGCTTC[G/T]TCCCTCACCAACACA	84900
rs556759371	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792016	AATTATTAGACCGCG[A/G]TCCTTCCCGTGTATG	84900
rs556770535	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116838366	ATTAGCTCTTATGGG[C/T]ATGCATCCCATTTCA	84900
rs556773009	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828255	CTCAAACTTGGATGT[G/T]CACTCGGGTCACCTG	84900
rs556792057	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744924	GAGAGTGGCCTCCTC[A/C]TGGACCAACATGGGT	84900
rs556832296	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809242	CCTGGGAGCAGAGTC[A/G]TGGCTGCATCCCAGT	84900
rs556846192	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776679	CCAGCCCAGCTGAGT[A/G]TTTCCAAAGCATATA	84900
rs556851004	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807178	TAGCAATCTCTGTAC[C/T]GGGGTGATTATCCCT	84900
rs556856653	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116797539	AGCCTGTCTATCTCA[-/A]AAAAAAAAAAAAAAG	84900
rs556880967	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792356	CGCCCAGCCTAGAAA[A/G]TTTCTGAGAATTAAT	84900
rs556952771	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738942	TCTTGAAAAATATTT[A/G]TATAATGACCTTTTC	84900
rs556956927	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818210	CACCTGTGGTCCCAG[C/G]TACTCGTGGGGCTGA	84900
rs556975221	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832440	CTGTTGTATAAATAC[A/G]CCATCATTTGTTTAT	84900
rs557036503	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825650	CTGGCCTTGTGGGAA[C/T]ATTTATACCACAGAA	84900
rs557048187	snp	C/T	5.80052e-05	0.00538509	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737882	GCCGGCGCCACACCA[C/T]GGCCGCCAGGTTCAC	84900
rs557051672	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116801950	CCTCAGCCTCCTGAG[A/C]AGCTGGGATTACAGG	84900
rs557090337	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771375	TAGGGTGGGAGGATC[A/G]CATAAGCCTGGGAGG	84900
rs557109971	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831578	CTGTAGTGACCATTC[C/T]TATAGGCACATCTTT	84900
rs557264686	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851628	GCCTGTAATCCCAGC[C/T]ACTCAGGAGGCTAAG	84900
rs557265745	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845873	ACATCTTCCTATCTC[A/G]GGAGCTTTGCACAGG	84900
rs557272830	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116758300	GTCTTTTAAGTGGAG[C/T]ATTTAGGCCACTTAC	84900
rs557321764	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765007	TGAGAGGATCTCTGT[A/G]TCCATGGACGGGCCT	84900
rs557379604	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809944	CCTCCCAAAGTGCTG[G/T]GCTTGCAGACGTGAG	84900
rs557439433	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750871	ATATTATATATATAT[A/T]ATATATATATTATAT	84900
rs557454371	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770740	ATTTTTTTATTTTTA[A/G]TAGAGATGAGGTTTC	84900
rs557460290	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776354	GTCAGATCTTCATTT[A/G]ATCATGATCATGGAA	84900
rs557483659	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784523	GCTCTTTCATCTGGG[A/G]CCTGGGTTGAACCAG	84900
rs557507689	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116751408	AGTATACTGTTTTCT[A/G]TTTGTTTGTTTTGAC	84900
rs557508721	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755643	TGCCCTTAACTTGTT[G/T]GTTTACAACAATGCC	84900
rs557508736	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748310	CTGCAGGCCTAACTC[C/T]GGGCTCTCTGCTCCG	84900
rs557520267	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779018	CAGAGAGGTTAAAAG[A/G]TCCACGTGAGGTCAC	84900
rs557570465	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791672	ACAATTTGTTTAGCC[A/G]TTCCTCTGTCAATGG	84900
rs557571686	in-del	-/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116762614	AGATGAAGTCTCACT[-/C]TGTCACCCAGGCTGG	84900
rs557596633	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116768247	CTGGGATTACAGGCA[C/T]CTGCCACCATGCCCA	84900
rs557620090	in-del	-/TGGA	0.00953873	0.0683987	intron-variant	RNFT2	GRCh38.p7	12:116839293	TGTCTCAGTAAATAT[-/TGGA]TGGATGGATGGATGG	84900
rs557659149	snp	A/G	0.000208659	0.0102121	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849349	CCTCTGCCTGTGGCT[A/G]GACCGTGAGCGCACC	84900
rs557664317	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116845418	GTACTTACATTTGCA[A/G]GAGACAGTAACAGGA	84900
rs557674907	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765725	TCCTGGGGACTAGAC[A/G]GGAATGAGGCTGAAG	84900
rs557697480	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811165	TTTCCAGCTACTAGG[A/G]AGGCTGAGGTGGGAG	84900
rs557697911	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116804084	TAGACGTTACCACTG[A/G]TTCCTTACTTTTACT	84900
rs557701202	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116814081	ACCCCAGCCCTCCCC[A/G]TGTCATTCTCCAGGA	84900
rs557704515	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799201	GCTCCTAGAAGCCAC[A/G]CTCCAGTCCTTGTAC	84900
rs557765908	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799741	GTGGGCAGATCACCT[G/T]AGGTCACCTCGTGTC	84900
rs557768196	snp	A/C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116752613	CCAGGTACGGTGGCT[A/C/T]ACGCCTGTAATCCTG	84900
rs557795205	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842111	GCTGCATCCAAGCTC[C/T]GCCGTGTGGTTGCTG	84900
rs557809612	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116763044	CTATGATTGCACCAC[C/T]GCACTCTAGCCTGGG	84900
rs557812108	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808023	GCCCAGGCTGGAGGG[A/C]AATGGCACGATCTCA	84900
rs557841322	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116806678	TGAGCCTGAGAGTTC[A/G]AGGCTGCAGTGAGCC	84900
rs557864090	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116778437	GACGCCCCTGGGGTT[G/T]TGTCTGCTTCCCCTT	84900
rs557875588	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775175	TGAGGCAGGAAAATC[A/G]CCTGAACCGGGGAGG	84900
rs557903291	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116793006	CTTTCTTAATCATCC[C/T]GCTGCCAATGCCAAT	84900
rs557923538	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842686	TCAAGCGATTCTCCT[G/T]CCTCAGCCTCCCGAA	84900
rs557929332	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803881	TTTTTGGCCCAAGGC[A/G]GTGGTGCAGAACACT	84900
rs557934826	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801104	GCTGTTATTGTTCCC[A/C]TTCCACAGATGAGGA	84900
rs557944438	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116795145	GCCCGGTGGCTCATG[C/T]CTGTAATCCCAGCAC	84900
rs557955936	in-del	-/ACC	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116791051	TCACAGTGTTGTACA[-/ACC]ACCACCTCTGTCTAG	84900
rs557972411	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827593	TCCTGCCACTTGTTT[C/T]TATAAATAAAGTTTT	84900
rs557984800	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833374	GCCCCTGAGAGCAGT[C/T]GCCTGTGATGCTCGA	84900
rs557987538	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116762606	TTTTTTTGAGATGAA[A/G]TCTCACTCTGTCACC	84900
rs558072450	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808718	TTTAATTCATTTTCT[A/G]TTGAACCAAATGATA	84900
rs558103383	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796808	TGGCTGCATAACATT[A/C]TGTGTGTAAAGACAC	84900
rs558142078	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116797262	GGCTATATTTGGAAA[C/T]AGGGTCTATAAAGAT	84900
rs558162084	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753255	TCCTGGGTTCAAGCA[A/G]TTCTTGTGCCTCAGC	84900
rs558237936	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760104	GTTGCTTCTGCTGAG[C/T]CATGCAGGTTGTCAG	84900
rs558294380	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787349	GAGCAAGTCGCTTAA[C/T]GTGAGCATTTTCCTC	84900
rs558329043	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740055	TACTAAAAATACAAA[A/C]ATTGGGTGGGCGTGG	84900
rs558383180	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841315	AAAATTAGCCAAGTG[C/T]GGTGGTGCACGCCTG	84900
rs558429905	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747537	CGTCTCACTCTGTGG[A/C]TAATGGTCTCATATA	84900
rs558455756	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116843985	TAGAGGGCAGGGCAG[A/T]TGTTGACTAAGCATT	84900
rs558455874	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753865	TTTTTTTTATTTTTC[C/T]CTCTCTTCTGTCAAC	84900
rs558462862	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116827081	AAAAATTAGCTGGGT[C/G]TGGCAGCAGGTGCCT	84900
rs558469330	snp	C/G	0.00398564	0.0444627	upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116737983	GGCCCCTACGCGCCC[C/G]GCAGCCCCATCCCTC	84900
rs558514638	snp	A/G	0.00306807	0.0390464	intron-variant	RNFT2	GRCh38.p7	12:116748646	ACATTACTCTCTGCC[A/G]CCCACCCAATGTCAG	84900
rs558516768	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116846567	AGTGCTGGGGTTATA[A/G]GCATGAGCCACTGTG	84900
rs558522809	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116837797	TCTTAGCTTTGACAA[A/G]TGTACCACGGTAATG	84900
rs558530217	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783264	TCCCAGCTGTCTGAC[C/T]TCTGAGAATCCTAGC	84900
rs558550594	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776767	ATTCAGTCTGGCCCT[G/T]GCCCAGAGCCTGTAA	84900
rs558577166	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116814080	GACCCCAGCCCTCCC[C/T]GTGTCATTCTCCAGG	84900
rs558578008	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845115	CAGGCATGGTGGCAC[A/G]TGCCTATAGTTGTAG	84900
rs558582799	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116809119	CACCTAGTCCTTGCT[-/G]GAGCCATCCAGTGCC	84900
rs558592803	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830524	AACTCCTGGGCTCAA[A/G]GGATCCTCCCACCTT	84900
rs558611445	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842434	TTAGCAGCTGTGTAC[C/T]TTGGGCGCACAGCTC	84900
rs558643877	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116789824	GGAAGGAGAGTGGAT[A/G]GGTGGATGGGTAAAT	84900
rs558646892	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807833	TTTTGAGATAGGGTC[C/T]TGCTGTGTCACCCAA	84900
rs558661471	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782744	TTATTCCTACCACCC[C/T]CTTTCTCACATGCCG	84900
rs558676997	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116742278	TTCTTTTTTTTTTTT[C/T]TTTTTTTGAGATAGG	84900
rs558716998	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736654	ACAACAGCATAACCC[A/T]TTATCCTGGGTGCAC	84900
rs558727601	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829883	ACCATGCCCAGACTC[A/G]TTTCCCCTCTAATTT	84900
rs558754342	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802302	TGGGACCCTTTTATT[A/G]AGGAGCACAGCATCT	84900
rs558801551	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836104	CCCCTTCCTCAGCCC[A/G]CAGATCTCACAGTGC	84900
rs558810244	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779035	CCACGTGAGGTCACA[C/T]AGCAGGTTAGTAGCA	84900
rs558811670	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784318	GTCGTGTCCTCTTAC[A/G]ATTCCCCAGTTCAGC	84900
rs558814664	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116777329	ATCTAAAGCCAGGAT[A/G]TTTTAGCCACTATTA	84900
rs558823779	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737605	AGATAAGGAAGGAGG[G/T]GAGGTAGGAAGAAGG	84900
rs558859066	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116751223	CCCGGCCTACTATAT[C/T]TGTTATTAACACACA	84900
rs558894451	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116833167	TAAGTGATCCACCTG[C/T]CTGGGCCTCCCAAAG	84900
rs558917568	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116762813	GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	84900
rs558961788	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835724	GGAAATAGGCACTAT[A/G]CATGCCATATATTTG	84900
rs558972380	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828904	CCTACAGGGGACTCA[A/G]GAAGCCAAGCTGGCA	84900
rs559007574	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788821	AGTTTGGTGGATGGA[A/T]GGATAGATGGATGGA	84900
rs559023998	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771885	AACGAGACGCTTCCT[C/T]CACAAATCTGCCAAC	84900
rs559054261	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772739	ATATTTGTTGTGGAA[C/G]TTGTAGTGTGCAGAA	84900
rs559071988	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809392	CTTCATGTGGCCTGG[C/G]GGGTCCAGCGCTTCT	84900
rs559179012	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767169	AATCAATTATAATAA[C/T]TGATTTTATTTAACC	84900
rs559196311	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850212	AGGCTGGAGTGCAGT[A/T]GGCACAATCACAGCT	84900
rs559205021	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815763	TGGACATCTTTGGGG[C/G]GGGGGCATTATTCAG	84900
rs559224582	in-del	-/A/AA	0.116047	0.211085	intron-variant	RNFT2	GRCh38.p7	12:116800634	CAAGACTCTGTCTCA[-/A/AA]AAAAAAAAAAATGGT	84900
rs559338438	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784927	TGATTGTCCTCTCCT[A/G]TCACTTCCCCTCACC	84900
rs559341518	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811986	GTGAGTGAGTTCACC[A/G]GGTCAAACTCTGATG	84900
rs559343308	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116759509	TCAGACGGAAGGTCT[A/G]GGGCTGAAGGCTGTT	84900
rs559369679	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738509	TTGTTCCCGAAGTGC[A/T]CCTGCCGGCTTCCAG	84900
rs559396003	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116820628	TTCTTTCTCTTTCTC[A/C]CACATCTTACTTTAT	84900
rs559444276	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116824594	ATCCAAGTTCCAGAC[A/G]GTAGGATAGAGAAAG	84900
rs559448573	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817722	CTTTTGAACTTCCTA[G/T]AAAGTATGGAGTAAG	84900
rs559493557	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116831241	AATATCCTTCAACTT[C/G]GATATGTCTCTTGTT	84900
rs559507570	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818285	CTGAGATCGCACCAC[C/T]GCACTCCAGCCTGGG	84900
rs559546697	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764760	AGCTGGGCATGGTGG[C/T]GGGCGCCTGTAATCC	84900
rs559570959	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752857	CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACAGT	84900
rs559586423	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116743452	TTTTGTATTTTAGTA[A/G]AGATGGGGTTTCACC	84900
rs559598486	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839701	GTGACAGTGTGGGTG[A/G]GCAAATGAATGGACA	84900
rs559645336	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760184	AAACGAAGGGCCGGT[C/T]TCACTCCCACCATGC	84900
rs559660115	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784815	TAGTGCTCGCCACCA[C/T]GAGACCAAAGTAGTC	84900
rs559702004	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747978	GGCAGATCACATGAG[C/G]TCAGGAGTTCAATAC	84900
rs559727964	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842141	GGTAGGATTCCGTTC[C/T]TAATGGGCTGTGAAA	84900
rs559730639	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116752360	GAAAGCTGGCATCTT[C/T]CCCACTACCCTGAAT	84900
rs559769605	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838142	GCTGCATAATGTGCC[A/G]TTTTATGAATAGACC	84900
rs559779805	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791746	GCTGTGAGCTTTCGC[A/G]GACAAGTATCTGTTT	84900
rs559809128	in-del	-/GG	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116841986	AGAGAGAGAGAGAGA[-/GG]GAGGATCCAGGTACA	84900
rs559830478	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830766	AATACAAAAATTAGC[C/T]GGGCATGGTGGTGTG	84900
rs559861529	snp	A/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116841523	GAGGGTGAGGCAGGC[A/G]GATCACCTGAGGTCA	84900
rs559887702	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831753	TACAGTAAACTGCAC[A/G]TGTTAGGAGTGTATA	84900
rs559891206	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803268	CGACACCACCTGCCA[C/T]GGGGGTGATGTTTTA	84900
rs559908216	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785566	CAAAGTACTTGTGTA[A/C]TTATTACATTCATTC	84900
rs559937825	in-del	-/A	0.257176	0.249897	intron-variant	RNFT2	GRCh38.p7	12:116766116	TCTCTAAAAAAAAAT[-/A]AAAAATTTTTTTTTA	84900
rs559985366	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116823690	TCTGTCTAAAAAAAA[A/T]AATAATAATAATTCT	84900
rs559987745	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748357	AAGAGCTACAGAATC[C/T]TTTGCCTGATTCCAA	84900
rs560019648	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741244	TTCAACGCATAATAG[A/C]TTGCTCTTTCTTTTA	84900
rs560029078	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775781	GGCACAGTGGCTCAC[A/G]CCTGTATTCCCAACA	84900
rs560098511	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116782876	ACCACTCCTTGTTGG[C/T]TTCCCCAAACCCTGC	84900
rs560145577	snp	A/C	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116794378	CAAGGCAGGCGGATC[A/C]CTTGAGGTCAGGAGT	84900
rs560154224	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761814	ACCTGCAGACCCTCA[A/G]TTAGGTTACCTTGGT	84900
rs560232412	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116787685	TGTCACTACACTCAG[C/G]CTGGGCAATAGAGGG	84900
rs560234527	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794747	TAGCCCAAGATCCCA[G/T]AGCTATGCTGTCTAA	84900
rs560265315	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782258	GCTCAATGGCTCAAA[A/C]CTGTAATCCCAGCAC	84900
rs560271760	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116812638	CTCCTGGGTTTAAAC[A/G]GTTCTCCTGCCTCAG	84900
rs560281093	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116839443	GATGGATGGATGGAT[C/G]GATGGATGGATGGAT	84900
rs560304248	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776358	GATCTTCATTTGATC[A/G]TGATCATGGAAGCAC	84900
rs560369160	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834952	CCTCCCGGGTTCAAG[C/T]GATTCTCATGTCTCA	84900
rs560382635	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821023	AAGAAATGGGAACGC[A/G]TCATAACTACCTACA	84900
rs560435136	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820215	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGTCTA	84900
rs560435958	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853439	AGGTGCATCAGCTTC[A/G]GAAGAGAAGAATGAT	84900
rs560488717	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739593	TTTGCCCTGCGGGAC[A/C]AAGCCCTGCCACATT	84900
rs560544160	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761117	CAGTCCCTTTACGCC[A/G]CAGACATTCAGCTCA	84900
rs560579376	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116763197	AAAAAAAAATCTCAT[C/T]AGAAAGTGGCCTAAG	84900
rs560630198	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790986	AATAAAACAATAAAA[A/G]TAAACCATTAATCAT	84900
rs560669913	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116833442	GGGCAGGGACTGTGC[C/T]CCCACCTTGGGCTTT	84900
rs560689032	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784327	TCTTACAATTCCCCA[C/G]TTCAGCTCTTGGGAG	84900
rs560692610	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768380	TGCTGGGATTACAGG[C/T]ATGAGCCACCGCACC	84900
rs560762122	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116774691	GGCTACCCATAAAAG[C/T]AATTTGAGGACTCAG	84900
rs560772150	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116749683	ATCTTTAAACAGGGT[C/T]ACATTCTGAGGTCCT	84900
rs560798962	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775294	AGAGAGAGAGAAGAG[C/T]AACATAGCTGAGTCC	84900
rs560851909	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830021	ATATGAGCATTTGCT[G/T]GGGTCAAATGATATC	84900
rs560856703	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737667	AGAAAGGAAGGGAAG[A/G]GGTAGGAAGACAGGG	84900
rs560868146	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817523	GTATAACCTTGTCCC[C/T]TCCACGCCTAATTTC	84900
rs560871987	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810169	CAGTCCAGTGGGGGT[A/G]TTGCAGGCAAGGAAG	84900
rs560945881	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851514	GAGGCTGAAGCAGGC[A/G]GGTCACCTGAGGTCA	84900
rs560967227	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743346	ATCTCAGCTCACTAC[A/C]ACTTCCGCCTCCTGG	84900
rs561039559	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116765451	GTCTGGAGACACTGT[G/T]TATTGAGCATTTACC	84900
rs561044206	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769129	CTTTGGGAGGCCAAG[A/G]TGGGCAGATCACGAG	84900
rs561105431	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116740071	ATTGGGTGGGCGTGG[C/T]GTCGCATGCCTGTAA	84900
rs561121525	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116803499	AGAAATAAAAGCCAC[C/T]CCGCTGACCCCACTT	84900
rs561150171	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758029	GTGCATATATATTTA[C/G]AATTGTGATATTTTC	84900
rs561169395	snp	A/G	0	0	intron-variant	RNFT2	GRCh38.p7	12:116809430	CCGAGAAGATCCACA[A/G]TCTTTCCAAAGCCCC	84900
rs561193631	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116764765	GGCATGGTGGTGGGC[A/G]CCTGTAATCCCAGCC	84900
rs561209311	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116763989	TGGGTAAAGAAACTG[A/G]TATATGTATATGATG	84900
rs561320441	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809141	TCCAGTGCCCTCCCC[C/G]AGGAACTGAAGAACA	84900
rs561323058	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116745779	TTAGTATGCCTGTTC[A/G]TGTATTCTTTCAAAC	84900
rs561324130	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814453	CATTCATGCAAAGCC[C/T]TGAAGGAAGCAAGGG	84900
rs561359662	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760304	GAAGAGGGTTTAGTT[C/T]GTGCCGCCGCTGTGG	84900
rs561387153	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815089	ATTTTACACTGGGTA[C/T]CATAAATGATGTAGC	84900
rs561401879	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844330	CCACCTCCCAGGTCA[C/T]GGTTCAAGCAATTCT	84900
rs561448398	in-del	-/TTTT			intron-variant	RNFT2	GRCh38.p7	12:116850149	CGTGCCCAGGCTCAC[-/TTTT]TTTTTTTTTTTTTTT	84900
rs561458188	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116771801	TGGATTACTTAGCCC[C/T]GACTTATCATCAGCT	84900
rs561472974	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756917	GGTACCAATTCTTCG[A/G]ATGTCTGGTAGAATT	84900
rs561473520	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836540	ATGGTGTAACATCAA[A/T]ATATCCTGCATGTGA	84900
rs561474131	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767338	ATCCTCCCACCTCAG[C/T]TTCCCAAGTAGCTGG	84900
rs561512450	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116852282	ATGGAGGAGCTTTGT[A/G/T]GCCACCTCGCTGTCA	84900
rs561571904	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116779366	AGGCACTGGCTGCGG[C/T]CACAAGGTAGCCCCA	84900
rs561576219	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798892	ATAACAGTACCTACA[C/T]GTGTTAGTTTTCATT	84900
rs561614204	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843638	CCTCCCCCTTCCTCT[A/G]TAGACGTTCATCCCT	84900
rs561648755	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116845274	ATATATATATATATA[G/T]AGAGAGAGAGAGAGA	84900
rs561652738	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116806059	GGGCAGCTTTGAAGC[C/T]GGCGCTGATGTTTTA	84900
rs561673517	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116749441	CGCCACCATGCCTGG[A/C]TAATTTAGCTCTATT	84900
rs561707154	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763734	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	84900
rs561714943	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806974	CTTAAGTGTTCCTCT[C/T]CCTTTTTACATGGCT	84900
rs561722810	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116744288	GAAGATGCAGAAACA[A/G]CATCCGGCTTGTAAT	84900
rs561725496	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811683	ACCCGGCATGCGTGC[A/G]CGTGCGTTTGTGCAT	84900
rs561730496	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853330	CTGACTCAAGTTCCA[C/T]GAAGTCCTTAGAAAT	84900
rs561753467	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838740	GGTGAAAGTCTGACA[A/G]GCTCTCTAAGCCTCA	84900
rs561783749	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819002	GGAGGTCCGGGTTCC[C/T]GCGCCACCCTTCCCT	84900
rs561792334	snp	G/T	0.0460142	0.144533	intron-variant	RNFT2	GRCh38.p7	12:116806401	ATATATATATATATA[G/T]ATAGATAGATAGATA	84900
rs561812055	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773540	AAATTAAAGACAGAG[C/T]GCTTCTGGTTGGCTT	84900
rs561829629	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845577	GGAAGGCTGTGAATA[A/T]GCCATGGGTTGAAGG	84900
rs561852342	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116775848	AGGAGTCTGAGACCA[A/G]CCTGGCCAACATGGC	84900
rs561857023	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833593	GGCTGCTGGGTGGCG[A/G]GTGAGGGCAGTGGGC	84900
rs561874513	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116793268	CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTTACC	84900
rs561893265	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838375	TATGGGCATGCATCC[C/T]ATTTCACACACACAT	84900
rs561908594	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747108	GTCACCCAGCCTGGA[A/G]TGCAGTGGCGTGATC	84900
rs561932682	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116839887	CCCCCTGAGCTAGGG[C/T]TCAGGAAGCAGATTG	84900
rs561984999	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116847641	CAAGTGATTCTCCTG[C/G]CTCAGCTTCCCGAGT	84900
rs561992747	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840706	TTTCATTGTGACCCT[C/G]ACCCTCCATGTCATC	84900
rs562002061	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758636	TTAGTTTCACTGGAT[A/T]CAAAATTCTTGGCTA	84900
rs562008291	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738197	GGGGCGGACAATCGC[G/T]TGAGTGCTGCGGGCG	84900
rs562008605	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745033	ATGGTGTTTGCTGTT[A/G]TTGTCATTATTAATA	84900
rs562017207	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791788	TTGTGGTAAATACAT[A/G]GGCAGAGAATTCTGG	84900
rs562058011	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116797701	CTTTATTGAAGAGGC[A/G]TTACAGCTCAGGCAG	84900
rs562068876	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798064	CAAGTCCCGCCTGCT[A/G]CCTCACTAGGACGGG	84900
rs562100874	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752067	TCCATGAGAAAATAT[C/T]GGTCAGGTGTGGTGG	84900
rs562123361	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116831072	TGTTGGGCCCCTTCA[A/G]CTTGGGGCCAGGTGC	84900
rs562126180	in-del	-/AAAATAA			intron-variant	RNFT2	GRCh38.p7	12:116800854	AAAATAAAATAAAAT[-/AAAATAA]AAACCATTTAACAGA	84900
rs562144801	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772895	GTGCAGTGGCACAAT[C/G]TCAGCTCACTGTAAC	84900
rs562191094	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116792613	TAATGTGCCAGGTCA[C/G]CGCGTAATCTAGCCT	84900
rs562254763	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846283	TTTTTATATTATTGT[C/T]ATTTTTTTAGACAAG	84900
rs562271668	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116835135	GATTACAGGCATGAG[C/T]CACCCCACCTGGCCC	84900
rs562296842	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116795387	CACTCCAGCCTGGGC[A/G]GCAGAGTGAGACTCC	84900
rs562303216	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825797	TACAGATGAAGAAAC[C/T]GAGGGTCATAGAGGT	84900
rs562306853	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849122	CCACACCTGTCCCCT[C/T]CCCTGCTGTTTCATC	84900
rs562311673	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780618	TTTCTTAGATGAAGC[C/T]GCAGCTCTGGTACCC	84900
rs562386016	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116743391	CATGCCTCTGTCTCC[C/T]GAGTAGTTGGGACCA	84900
rs562397035	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116828579	ATGAGGTCTTAGTTA[C/T]CTTAGTACCTCCAGA	84900
rs562420925	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788492	CTTAGAAACCTACCC[G/T]GCCTCTTCAGGCTAG	84900
rs562475877	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842870	TGAGCCACTGTGCCC[A/G]GCGTGTTTATACTTT	84900
rs562491403	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741501	CACTTTCTGGTTCAC[C/T]GATGGCCATTCTTTT	84900
rs562506108	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782329	TTTGAGACCAGCTTG[A/G]GCAAGATAAGCCTGC	84900
rs562521422	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755284	TTATGTTCAGTTAGC[C/T]GTAAGTATTTTGGTT	84900
rs562621342	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787445	GGGCACAGTGGCTCA[C/T]ACCTGTAATCCCTGT	84900
rs562632952	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116830858	GCAGCGAGCTGAGAT[C/T]GTGCCACTGCACTCC	84900
rs562641355	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116748428	CACTGCAGGTCTTCC[A/G]TAGGAACTAGAGATA	84900
rs562679895	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815331	ACCACAAACCTTGTG[G/T]CTTAAAACAACACAA	84900
rs562722130	snp	C/G	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116840780	TTTTAAGAGTCATAT[C/G]AGATGATGTATAGGG	84900
rs562729519	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808206	CTGACCTCAGGTGAT[C/G]CACCTGCCTTGGCCT	84900
rs562822382	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781418	CTGTGGCTGCTGTGA[A/C]AAATTGCTACAAACT	84900
rs562847201	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738122	GGCTAGTCGCGCAAG[A/G]TCTTCTCACCATTGG	84900
rs562864417	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814257	CAGGCCCAGGACTAG[C/G]TCCCAGAAATACAGC	84900
rs562875872	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819815	TGGATTTTTACAAAC[A/C]TATGTAATCACTCAG	84900
rs562887009	snp	A/T	0.0134861	0.0810011	intron-variant	RNFT2	GRCh38.p7	12:116766121	TAAAAAAAAATAAAA[A/T]TTTTTTTTTAATTAG	84900
rs562906026	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775403	CCTGGGGACCCATTT[C/T]ACAGGTGAGGACACT	84900
rs562908964	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779268	GTGGGGATCGCAGAC[C/T]TTGTTCTGAAGTACA	84900
rs562927606	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800138	AGGCCGAGCATATGC[A/G]GGTGCCATGCTCCCC	84900
rs562956292	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116754401	TTGGTGGGCATTTGG[A/G]TTGGTTCCACAATTT	84900
rs563020917	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778619	CTTTGGAAGGCTGAG[A/G]CGGGTGGATCACTTG	84900
rs563050367	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815705	CACAAAATTCCTTTC[A/G]CCCTGTAAGGTACCA	84900
rs563065962	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116804529	GCAATTAGATTGTTT[C/G]TTTATTTTTTTACCA	84900
rs563080547	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848427	AATCATATCAGGTCA[C/T]TCCTCTGCTCCAAGC	84900
rs563088033	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762787	TGGCTAATTTTTATA[C/T]TTTTAGTAGAGATGG	84900
rs563101944	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849079	CCATCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	84900
rs563105658	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116805272	GGGCAGTTCTCTCTT[C/T]TTCCTAATCTTGATG	84900
rs563114928	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116817612	TGGGAAACCAGAATG[A/C]CAAACTTGTCACTAC	84900
rs563146805	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800658	AAATGGTTTAAAAAT[A/G]CAAAAAATTAGCTGG	84900
rs563242997	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804598	CACAAAAGTTTCTCT[A/G]ACACAGCCATCTAGA	84900
rs563252687	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116823571	TACCTATAATCCCAG[C/T]TACTCTGGTGGCTGA	84900
rs563261458	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771071	TATGGCAGAGACCAT[A/G]TAGCTTACAAAGCCA	84900
rs563426111	in-del	-/TGGCGTTG	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116753110	AACTTGAATTCCTTA[-/TGGCGTTG]TGGCGTTGTAAGTTT	84900
rs563434715	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763722	AGTTGGAACTTGCAG[C/T]GAGCCGAGATCGCGC	84900
rs563464772	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815097	CTGGGTATCATAAAT[A/G]ATGTAGCCGGTCCTA	84900
rs563467511	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764046	TGAATTAATGGAATT[C/T]GCAGCAACCTGGATG	84900
rs563471846	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830562	CAAAGTGTTGGGAGT[A/G]CAGGTGTCAGCCATT	84900
rs563489913	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759406	ATTGCTGGTGAACTA[A/G]TGTGATTTTGGGGGA	84900
rs563509107	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822320	GGCAAATGGCCCCAG[A/G]AGAAACAGGGTCTGT	84900
rs563528196	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116790915	GCAGTGAACCCTGAT[A/C]GCAGCACTGCACTCC	84900
rs563537240	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116850890	CACCTGCCTCAGCCT[C/T]CCAGAGTGCTGGGAT	84900
rs563550839	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851607	TAGCCGGGCGCGGTG[A/G]CGGGTGCCTGTAATC	84900
rs563600269	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116850323	CCAGGCCTGGCTAAT[-/T]TTTTTTTTTTTTTAA	84900
rs563607530	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818775	GTAACTTGACCTCTC[C/T]GAGCCTTGTGTTCTC	84900
rs563610687	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116805560	GCTCAGTATAACCTT[C/T]GCCTCCCGGGTTCCA	84900
rs563621734	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851852	TTGGTCTCCTGTCTT[C/T]ATGTCTTTCTCCTCT	84900
rs563624570	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770218	GGTGTATCTTTTTTC[A/C/T]TCCTTTATACAGTGT	84900
rs563660073	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802596	CACAAGACAAACAAT[A/G]CCACCAGCCACCAGG	84900
rs563681964	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116791108	GAAGGAAACCTTGTC[C/T]CCACTAAGCAGTCAC	84900
rs563691668	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116823552	AGCTGGGCGCCGTGG[C/T]GCATACCTATAATCC	84900
rs563708443	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116748295	CTGGGCTCTCCATTC[C/T]TGCAGGCCTAACTCC	84900
rs563736189	in-del	-/AGGG	0.0528381	0.153711	intron-variant	RNFT2	GRCh38.p7	12:116839774	GGAAGGAAGGAAGGA[-/AGGG]AGGGAGGGAGGGAGG	84900
rs563783383	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798057	CTGGAGTCAAGTCCC[A/G]CCTGCTACCTCACTA	84900
rs563796429	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844557	TTTAAATATGTCTCC[A/G]TTTCTATTTCTAAAT	84900
rs563816883	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824795	GAGCTCTACTCTCAT[A/G]ATCTAATTACCTTTC	84900
rs563857026	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821103	GGGGGTTACTCTTCC[C/G]CTGTTGCCTTCTCAC	84900
rs563867025	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116750727	GATTTTATAGTCTTC[A/C]TGGGATCACAGTGAT	84900
rs563876939	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847760	TCAAACTCCTGACCT[C/G]GGGTGATCCGCCCAC	84900
rs563887074	snp	C/G	0.00159617	0.0282053	downstream-variant-500B	RNFT2	GRCh38.p7	12:116854086	AGGAATCTGGCAAAA[C/G]GGATCAGAAAGGGCC	84900
rs563908044	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116825584	GTGAGAGCCAATGGT[C/T]ACATTTTCATGAAAT	84900
rs563912994	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751130	TATATTGCCCAGGCT[A/G]GTCTCAAATTCCTGG	84900
rs563923233	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116772352	TCGCTCTGTCACCAG[C/G]CTGAAGTGCTGTGGT	84900
rs563939463	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836645	TGGACATAATAGTGG[C/T]CAGGCACAGTGGCTC	84900
rs563948895	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116781927	ACTAAAAATACAAAA[A/G]AATTAGCTGGGCGTG	84900
rs563954810	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116799303	CCCCAAGCCCAAGAA[A/C]ACTCTGCTTTTAAAG	84900
rs563974624	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116793467	TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC	84900
rs563994036	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116754223	AACGTACAATGTTTG[A/G]TTTTCCATTCCTGAG	84900
rs563995056	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116776579	TTGTGAGTGACTTGT[C/G]AGTAATTTTGCCCTA	84900
rs564022396	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116790653	TTGAGATACAATTCA[C/T]GTAACATAAAATTAA	84900
rs564057213	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742638	AGAAATATTGGCTGC[A/G]TGTGTAAAACTTAGA	84900
rs564096983	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799959	CATGTGAATGGCGTG[A/G]TACCCTCCCCAAGGT	84900
rs564114331	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834881	TTTAGACCGAGTCTC[A/G]CTCTGTTGCCCAGGC	84900
rs564118812	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116767795	ATATTGGTCAAGCTG[A/G]TCTCAAACTCCTGAC	84900
rs564133088	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116832893	GTGAGTACCCAAGTC[A/G]TGTTCTTTTTTTTTT	84900
rs564183672	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747204	TGGGACTACAGGTGC[A/G]TGCCACCATGCCTGG	84900
rs564201042	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767743	CGCCACCACGCCCAG[C/T]GAATTTTTGTATTTT	84900
rs564236301	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116761025	GCCATTCTTCGGTCT[A/G]TCACCCCTGGGTAGA	84900
rs564255876	in-del	-/TC			intron-variant	RNFT2	GRCh38.p7	12:116822346	CTGTCTCTCTCTCTG[-/TC]TCTCTCTCTCTCTCT	84900
rs564262088	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116827333	GAAGGCTTTTCATAG[A/G]CGGTGACAGTTAGCT	84900
rs564266672	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116831956	CAACATGGTGAAATC[C/T]TGTCTCTACTAAAAA	84900
rs564281432	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787638	GGAGGATCATTGAGC[C/T]CAGGAGTTGAGGTTG	84900
rs564289637	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740379	CTCCCCTGACTGTGC[A/G]TCCCTCTGGAGACGA	84900
rs564378088	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116763004	GGAGGATTGCTTGAT[C/G]CCAGGAGTTTGAGGC	84900
rs564392002	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116794362	CAGCACTTTGGGAGG[C/T]CAAGGCAGGCGGATC	84900
rs564410993	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792246	GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG	84900
rs564439278	snp	A/G	0.000148447	0.00861404	intron-variant	RNFT2	GRCh38.p7	12:116836050	CTTCAGGTGGTCCCC[A/G]CCAGGGTCCTGAGAA	84900
rs564446884	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116785750	TTTATTTTCAGCAGA[C/T]GAAAATAAAACAGGA	84900
rs564525192	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116752143	TTGCTTGAGGCTGGG[A/G]GTTCGAGACCAGCCT	84900
rs564527963	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767393	CTGGCTAATTTTTAC[A/C]TTTTTTGTAGAGATG	84900
rs564606322	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116750787	CATTATTTTTACTAT[A/G]TGTGTGTGTGTATAT	84900
rs564611891	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752733	TAATTCAAAAATTAG[A/C]CAGGTGTGGTGGCAC	84900
rs564622976	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796053	AGCTGATATTACAGG[C/T]GCCCACCACCACACC	84900
rs564637730	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819044	CTGGGGCAGATTCCT[G/T]TATCCCTCTGATCCC	84900
rs564672629	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116774533	GCTGTCAGAATTGAG[A/G]GAAGATTCTTTTGTG	84900
rs564679314	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819663	ACGCGCGGCCACCAG[C/G]CCCGCCCCGCTGGCC	84900
rs564700413	in-del	-/TCTG	0.0134861	0.0810011	intron-variant	RNFT2	GRCh38.p7	12:116826002	AAAAAAGGTTTCATC[-/TCTG]TCTGTGCATTTTTCA	84900
rs564709566	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116806217	TCTACCAAAAATACA[A/G]AAATTAGCCAGGCAT	84900
rs564709903	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116742522	TCTGTCCGACTTGGC[C/T]GCCCAAGCTCCTGCT	84900
rs564713671	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796789	TAAGCCTCAGCTATG[A/G]TTTTGGCTGCATAAC	84900
rs564715557	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822021	TGTATTTTTGGTAGA[A/G]ACGGGATTTCACCGT	84900
rs564740612	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812796	GCCTTGGCCTCCCAA[A/G]GTGCTGGGATTACAG	84900
rs564790981	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843556	ACAATCCAGGGCCAC[C/G]TGCCTTCCCCACTGC	84900
rs564792283	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822193	TAGTTCTGATGACAC[C/T]GTCAGTCACAGTGCT	84900
rs564853593	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822869	AGCCATGGTGGTGCA[C/T]GCCTATAATCCCAGC	84900
rs564870798	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116783052	TGCTCAATACATGTT[A/G]GCTACCAGGGTGATG	84900
rs564880612	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736330	GGGTCACAAGACAGA[A/G]AAGGGACAACACGCG	84900
rs564929887	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749339	CTGGAGTGCAGTGGC[A/G]AGATCTTGGCTCACT	84900
rs564957085	snp	C/T	1.64863e-05	0.00287104	intron-variant	RNFT2	GRCh38.p7	12:116835943	ACATTTCAGCCACCA[C/T]CCTGCTCTCCTTTCA	84900
rs565014940	snp	A/G	0.000798403	0.0199641	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749985	GTTCCCCTCCAGCCT[A/G]GTGCTGGGCTCCTCG	84900
rs565036171	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742057	ATTTTTATTTCTTCC[A/G]TTTCTCAAGATGAAG	84900
rs565070795	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116760946	TGCAGTGGCATGACC[A/G]TAGCTCATTGTAGCC	84900
rs565108044	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764174	GCAAAGGCATAAGAA[C/T]GATACAGTGGACTTT	84900
rs565156349	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116839298	TCAGTAAATATTGGA[A/T]GGATGGATGGATGGA	84900
rs565186713	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795465	TTAGCCCAAGATCCG[C/G]GAACTGCGCTGTCTA	84900
rs565200383	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116816252	GCAGTTGCTGGGGCA[C/T]GTGCGCTGGGCCCTT	84900
rs565206719	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741182	TGAACAATACCTCAC[A/C]CTCAGCGTTAGTTGT	84900
rs565216419	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810239	ACCTAAACCAGTCCC[C/T]AGCAGAGACTTCCTG	84900
rs565263101	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814418	CTTTTAGACAGTGGT[C/G]GGGGGTAGGGAGAAG	84900
rs565303351	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769011	GCTGAGATTGCAGGC[A/G]TGAGCCACAGTGCCC	84900
rs565397749	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820893	ACCGAGAAACTCATC[A/G]CTAAACTAGAAGCCA	84900
rs565476171	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842981	GCTTTCTCGGCTCAC[A/G]CTGAACACCAAGTGC	84900
rs565488944	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842441	CTGTGTACCTTGGGC[A/G]CACAGCTCCCCCTCT	84900
rs565496011	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792276	GCTGGTCTTGAACTC[C/G]TGACCTCAGGTGATC	84900
rs565524025	in-del	-/A	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116769869	AACCCCGTCTCTACT[-/A]AAAAAAAATACCAAA	84900
rs565564639	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849191	CATTGTCTCCCCAAC[A/G/T]CGAGTGCAGGCGCCC	84900
rs565588802	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116748726	AGACTGCAGAGCCAG[C/T]GGTCCTTGGGATCCC	84900
rs565595329	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810356	GGACAGCCGCAGCCA[C/T]GGTGTGGAAGTGGAA	84900
rs565615997	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849566	GCCTCTTGCCCTCCA[C/T]CACCTCTGACCCCAA	84900
rs565632598	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116851610	CCGGGCGCGGTGGCG[C/G]GTGCCTGTAATCCCA	84900
rs565637751	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764827	AACCCAGGAGGCGGA[A/G]GTTGCAATGAGCTGA	84900
rs565646612	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116828416	ATAACTTCTCTTAGA[C/T]TTTGTTGATCAGTTT	84900
rs565652440	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116804672	CCAGAATCCCAAGAC[A/G/T]GTTCTTTCTCGAGGC	84900
rs565655491	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791856	TGTCAAACCTTCCCA[C/T]AGTGCCTGCACCATT	84900
rs565673750	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758203	ACCCCTTTAAGTTTA[C/T]GTGAGTCCTTATGTG	84900
rs565693348	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116758780	GGTGCTTCTGTCTCA[C/T]AGCTCTTAAGATTGT	84900
rs565696165	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116785325	TGAGACAAGGTCTTG[C/T]TCTGCTTCCCAGGCT	84900
rs565700052	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845763	AGAATCCAGTATGGT[C/T]TTCGCGGCTCTGTGT	84900
rs565708266	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825994	TACAGAAAAAAAAAG[A/G]TTTCATCTCTGTCTG	84900
rs565715528	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742768	CCTAGGTGACATGAG[A/G]AGATCCTGTCTCTAC	84900
rs565716734	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738311	CTGCCCAGGCTGCGC[A/G]GGTGATTGGCTTGGC	84900
rs565777061	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851229	CACATCTAAAAAAAA[A/T]TAAATTTATTAGAGA	84900
rs565788212	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811078	CTCCCTTCTCCATGC[C/T]TCAGTTTCCTCATCT	84900
rs565821348	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116843976	TTTACCACCTAGAGG[G/T]CAGGGCAGATGTTGA	84900
rs565860287	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745397	CCAGGCTGGTCTCAA[A/T]CTCCTGGCCTCAAGT	84900
rs565877916	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832118	CCTGGGCAACATAGC[A/T]AGACCTTGTCTCAAA	84900
rs565879865	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780777	AAGACCATGAATGAC[A/G]AGGACCTTTTGCCCA	84900
rs565880896	snp	C/G	0.00010016	0.00707602	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750210	TGGGACGCCCGCCCC[C/G]GCCCTGTCCGAGCTG	84900
rs565892967	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790689	AGGCTGGGCTCAATG[G/T]CTCATGCCTGTTATC	84900
rs565905320	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778741	CTGTAATCCAGCTAC[C/T]TGGGAAGCTGAGGCG	84900
rs565909343	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770563	CTTTTTTCTTTGTTT[C/T]TTCATTTTTTTTTTA	84900
rs565912190	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785833	ATGGGTGGATCGCTC[A/G]AGTTCATGAGTTCGA	84900
rs565939853	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751783	TTTTGTTTTTGAGAT[A/G]GAGTCTCACTCTGTC	84900
rs565952233	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829617	AGATGGAATATAAAA[C/G]TTGGCTATAAATCTC	84900
rs565987034	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784001	ACCACCATCCCATTT[C/T]CACAGATGTAGAAGC	84900
rs565995978	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116813125	CATGCCTGGCTAATT[G/T]TTTTTGTATTTTTTG	84900
rs566014957	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778143	TCCCTCCTTTCTTCC[C/T]TCCTTCCTTTTGCCT	84900
rs566019893	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116744735	AGTCAGGCTGAAATC[C/T]CGGCTGGATGCAGGG	84900
rs566062715	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116746977	GTCAGCCTTTTGTAT[A/C]TGTGGGTTTTGGTCC	84900
rs566125911	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748973	GGGAGGATTTAGTAA[A/G]TTAATCAATGCAAAA	84900
rs566181956	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746590	TGGGATGGGGTACGG[A/G]TTAGGGGAGACATCC	84900
rs566184702	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789834	TGGATGGGTGGATGG[A/G]TAAATGGGAGGAGAG	84900
rs566208802	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737490	AAGGGGAGGAAAGAA[A/G]AAAGGGAAGGGGGAG	84900
rs566214375	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840995	TTTTCGTAATTAAAT[A/G]CTTCAAACATCCTTT	84900
rs566270255	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747374	TATATATTTTAAAAC[A/G]TATTTCCTGGAGCCA	84900
rs566296692	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768023	AATATTTCTGGAAGG[A/G]CAACCAAGAAACTAG	84900
rs566296793	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775708	GTAAACAATAAAACA[G/T]TGGACATATATCACA	84900
rs566336582	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830147	CCTTCATTCCTCTTC[C/T]CCTAATGTTGATATC	84900
rs566339343	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768641	ATGCAATTATGTACA[C/G]TACCTAATGCTTGAT	84900
rs566344953	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116784407	AGCAGCTGGCCAATG[A/C]ATGGGCTGCACATGG	84900
rs566409749	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116823009	CTCAAAAAGCAAAAA[A/G]CGAAAAGACAAAAGG	84900
rs566409815	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816463	GGCCTCCTCCTCCCC[C/G]TCCTCGCCAGAAGAG	84900
rs566427460	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833108	ATTTTTAGTAGAGTT[A/G]GGGGTTCGCCATGTT	84900
rs566469632	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116826633	ACGGGGTGCCACATA[A/G]GCTCTCACTCTCCTA	84900
rs566517855	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738406	TTTTTTCTTTTCTCC[C/T]ATCATGGTCTGTGTA	84900
rs566523565	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116819207	AGGGGTCTTCGGGGT[G/T]AAATGTCCAAATAAG	84900
rs566588320	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116781489	TGGAGGTTAGGAGTC[A/C]AAAGTGGGTTTTACT	84900
rs566623429	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827355	CAGTTAGCTGAGACC[C/T]AAAAGATGAATAGAT	84900
rs566647493	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116843843	CAGACTTTCCTGTTT[-/G]GTCATTTGTCATCTG	84900
rs566695242	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116809034	GTGGTTATAACTGGA[G/T]GCACAGGGCCGGAGC	84900
rs566745407	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116840360	CTTGCCTGAGGTCCC[A/G]TTGTTCCTCAGTCAC	84900
rs566757984	snp	A/G			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836323	TGGAGACCAAGGCTG[A/G]GGGAGAGTAGGACCC	84900
rs566761675	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116746406	AGCCACAGGTCTCAA[G/T]GGAAAGATGAGGAAT	84900
rs566784040	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116852334	TCCCCCTGCCCCGCC[A/G]TAGATTCAGGACATT	84900
rs566883295	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774023	AACTTGAGGACATTT[C/T]GTGAATTGAAATAAG	84900
rs566919429	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809346	ATGAGAGGAGAGGTC[C/T]TTCCACTTCGTTGTG	84900
rs566924602	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738830	GTTAAATGTGTGGAT[A/G]AGAACTTTGGAATAT	84900
rs566981024	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808485	TCTGCCACCAAGGGA[C/T]GCAGCAGGGACAGGG	84900
rs567048587	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116743193	TTTGGCCCTGTGATT[A/G]ATAGATACCAGGTAG	84900
rs567093430	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739533	AGGGCAATATTACGG[A/G]GAGTCAGGAGAATGA	84900
rs567100950	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116792823	GGCTCACGGCACAGA[G/T]GCTCTTTGCTGGGCC	84900
rs567115231	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799663	TTCCTCAGCTGGGCA[C/T]GATGGCTCATGCCTG	84900
rs567128627	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836867	CGCGGGAGGCAGAGG[C/T]TGCAGTGAGCCGAGG	84900
rs567145745	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852878	GGTTACTAGTGAATA[C/T]CCCAATGGTTTCTCC	84900
rs567160101	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116784359	AGGTCTGATTGGCCC[C/T]GGTCATTTTGTGTAC	84900
rs567183450	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809645	TTCACCCCTGCCCTC[G/T]TTTTCACAGACCGGT	84900
rs567190707	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760498	CTGGGGGACCCAGTG[A/G]GCTCCCAGGGCCTTG	84900
rs567190942	snp	A/C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116808611	CTGGCTCCACACCCC[A/C/G]CAAGCTGTTGTTCCG	84900
rs567223665	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116821643	GGAAAAGTCTCGCAG[A/G]AGGCTGAGGGCCCCC	84900
rs567229775	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116777147	GGTCTCAAACTCCTG[A/G]CCTCAAGTGATCTGC	84900
rs567237794	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776030	CCTGGGCAACAGAGC[A/G]AGACTCTCAAAAAAA	84900
rs567265235	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844111	CATTATTGGCCTTTT[C/T]ACTCTGGTTCTTTCA	84900
rs567273818	snp	A/C	0.00795532	0.062565	intron-variant	RNFT2	GRCh38.p7	12:116763784	ACTCCATCTCAAAAA[A/C]AAAAGGGGGCGGGGG	84900
rs567334752	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736443	ATAAAAGGGACTTAC[A/G]ACACTCAGCCTCTCT	84900
rs567362276	snp	C/T	0.000347011	0.0131676	intron-variant	RNFT2	GRCh38.p7	12:116750339	TGGGTGTCCTAGCCA[C/T]GGGCTTCACAGGCAG	84900
rs567393407	in-del	-/TTCA	0.00430208	0.0461794	intron-variant	RNFT2	GRCh38.p7	12:116809191	AGCTGAGTTTGTTCA[-/TTCA]TTCATTCATTCATTC	84900
rs567455924	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762945	AAGTTAGCCAGGTGT[C/G]GGGGCATGTGCCTGT	84900
rs567473836	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789427	GTAGGAGAGTGGTGG[A/G]TGGATGGATGGTAGA	84900
rs567475235	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116757183	AATATCTCCTGTTTC[A/G]TTTCTTAGTGAGGTC	84900
rs567505855	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116849261	CCTGCTCCCGAGACC[A/G]AGGCAGACGCTCAGT	84900
rs567530784	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821156	TCTTTCTCTTCTGGC[C/T]TCTAACTCTGCCATT	84900
rs567540427	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756608	TTTTTGTTTTTAATT[A/C]TGTTTACGTGGTGTA	84900
rs567556135	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764295	AAAATCTCACAAATC[A/G]CCACAAAAGAACTTA	84900
rs567556234	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116840413	GCCTCTGATGCCATT[G/T]GCCATGCCCATTCCA	84900
rs567577557	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737212	GGGCAGGTCCCTCAC[C/T]CGTGCTGAGACCGGG	84900
rs567577973	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755487	GTGGAGCAGGCTGGC[A/G]CTTGAGTTGAACCCA	84900
rs567622750	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841651	TACTCGGGAGTCTAG[A/G]GCAGGAGAGTCACTG	84900
rs567635616	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116788689	AGTATCTGCTGTGTA[C/T]CCAGAAGTGTTCATT	84900
rs567639420	in-del	-/A	0.226779	0.248919	intron-variant	RNFT2	GRCh38.p7	12:116798225	ACGAGACTCTGTCTC[-/A]AAAAAAAAAAAAGAA	84900
rs567675064	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808559	GATGAAGATGGTGGG[A/G]AGGTTTTGGGTGATT	84900
rs567683416	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842514	GGTGCAATTATGCAC[A/C]TAAAGAACATTGGCA	84900
rs567745532	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792325	AAAGTGCTGGGATTA[C/T]AGGTATGAGCCACTG	84900
rs567747922	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116762293	GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA	84900
rs567768955	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800232	CCGGGCATGGTGGCT[C/T]ATGCCTGTAATCCCT	84900
rs567770224	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828643	CAGAAATGGAAGCAA[C/G]GATGGGAGGGAAGAA	84900
rs567804247	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116783096	ACTATGCCCATCTTT[C/T]CTCCTCCTACTGCTG	84900
rs567805318	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758924	TAGCAAGGCCGGGGA[C/T]GTTTTCCTCGATTAT	84900
rs567814658	in-del	-/TTTG	0.0096203	0.0686848	intron-variant	RNFT2	GRCh38.p7	12:116842572	TTATTTATTTATTTG[-/TTTG]TTTGTTTGTTTGTTT	84900
rs567835618	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742159	AAAAGCATAGGCCAC[A/G]GCCTTTATTGTGTTT	84900
rs567891669	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776611	TCAAAATAACCCAGA[A/C]CAATCCGTTCTTAGG	84900
rs567920585	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116748835	AGTCGGCCTGGGTTC[A/G]AATCTCCCCTGCTCC	84900
rs567944568	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835448	TAAAAATCCATACAT[C/T]CTTCTCTTTCTCTTT	84900
rs567986352	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744745	AAATCTCGGCTGGAT[A/G]CAGGGGAGAGGCCCA	84900
rs568017527	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116822491	CTTTTCTGTGCCTCC[A/T]TTTCCTTATCTGTAA	84900
rs568025072	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804785	CAGCCTAGGCAACAC[A/G]ACAAAACCTTGTCTC	84900
rs568064629	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116797930	CCTGGGTTTTGCCAT[A/G]GCAATGGTAAACTAA	84900
rs568068545	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839109	GTCACGTCCCTGGCT[A/G]TATGGTCTCATAGAT	84900
rs568089434	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751852	CAAACCTCTACCCAC[C/T]GAGTTCAAGTGATTC	84900
rs568113813	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116780411	TGCAGTTCACAATAC[A/G]GTTCCCACTCCTAGG	84900
rs568166278	snp	A/C	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116793926	TCATGTGAGCAAAGA[A/C]CCCTAGGTTGCTCTT	84900
rs568169862	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116805501	GTTTTTTGACACAGC[A/G]TCTCTCTCTGTCGCC	84900
rs568178700	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116742827	GTGGTGCATACCTAT[A/G]GTCTCAGCACTTTGG	84900
rs568199181	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837543	TGCTGTTGTTATTGC[C/T]GTTTGGAGATTTGGA	84900
rs568247332	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739365	GTTGAGCGCCACTCT[A/G]TGCCAAACAGTGTCC	84900
rs568253674	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116743677	ACATACATCCAAGGG[A/G]CGGGCAGCCAAGCCT	84900
rs568264127	snp	A/G	0.0193772	0.0965046	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737550	GAAGGTGAGGAAGGT[A/G]AGGAAGGAAGGGAGG	84900
rs568269050	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116797222	ATATGTGTGTTGGAG[C/T]CCAAACCCCAGGACC	84900
rs568278555	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116764880	CTGGGCAACAAGAGC[A/G]AAAGTCCGTCTCAAA	84900
rs568283191	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780862	CATGGCCTGATGGCT[A/G]TGCCCATGGACTTTG	84900
rs568293715	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825447	CATTTCTGGATTATC[A/T]TGAGGGCCAGTACTA	84900
rs568302024	in-del	-/T	0.00438332	0.0466095	intron-variant	RNFT2	GRCh38.p7	12:116827794	ATAGCAAGTGGGAAG[-/T]TTGGGATTTGGCCCA	84900
rs568316204	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765562	GCACGAGCTGTTGAG[A/G]ATCAACAGCAGAGGG	84900
rs568362548	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741463	GATGAAAGCTCCAGC[A/G]TATTCAGTGTCTGCG	84900
rs568372424	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823063	GAAGGCTCTTTGACT[A/G]TATTGTTTGACCTCC	84900
rs568394714	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833052	GTAGCCTCCGAGTAG[A/C]TGGGATTACAGGTGC	84900
rs568404875	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778889	ACCTCTTTCCTCTAT[A/C]AGTTACCCAGCCTAA	84900
rs568436479	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116764762	CTGGGCATGGTGGTG[A/G]GCGCCTGTAATCCCA	84900
rs568465669	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116813753	CAGATATTTCTCCCT[A/T]CACTATATTTTCTCT	84900
rs568497146	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116840421	TGCCATTGGCCATGC[C/T]CATTCCACAAGGCTT	84900
rs568507813	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116830300	TATTGTTGTTTTTTT[G/T]TTTTCGAGACAGGGT	84900
rs568565472	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116764553	AGGTCCTTCCTGACC[C/G/T]TTAGTCTCATCTTCT	84900
rs568585928	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791334	TTTCTTTTTTGAGAC[A/G]GAGTCTCACCGTGTT	84900
rs568601306	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116791485	CCTGGCTAATGTTTG[A/T]ATTTTAGAGAGATGG	84900
rs568616847	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116793442	CTCCTCCCACCTCAG[C/T]CTCCCAGAGTGCTGG	84900
rs568659256	snp	A/G/T	0.000434241	0.0147292	utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740455	CCCCTGAGGATTCCC[A/G/T]AATGCCTACCTCCAG	84900
rs568670682	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811132	GGCATGATGGCTCAC[A/G]CTACTCGGAAGTTTG	84900
rs568716483	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116779619	CTTGATGCAATTTTC[A/G]TCCACATTTCACCTG	84900
rs568743789	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817181	CCATGGCCGACTAAT[C/T]TTTGTATTTTTAGTA	84900
rs568823679	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781974	GTCCTACTTACTCGG[A/G]AGGCTGACGCAGGAG	84900
rs568824095	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820523	TGGAAAGTTCCTGTG[C/T]CCTCACTTCCCCCAC	84900
rs568843636	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116783778	AGGAGCAAGACAGGC[A/G]GAGCCCACAGAGTGC	84900
rs568909248	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812929	GGCAAGGGAGTCCTT[C/T]GGTTTTCTGTTTTGT	84900
rs568924130	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116847470	ACTTGTCCAAGTTAT[A/G]CAGCCAGAGAACGGT	84900
rs568926535	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116769219	CAAAAATTAGCTGGG[C/T]GTGGTAGCAGGTGCC	84900
rs568987493	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787740	AAAAAAAAAGATATA[A/T]TGTGTATAATGTGTG	84900
rs568987861	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781595	CTCTCCTCTCTCCCT[C/G]TCCCTCCCCCTACAC	84900
rs569016300	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116768342	CTGACCTCAGGTGAT[A/C]CGCCGGCCTTGGCCT	84900
rs569034080	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776399	GCAGAGTGTGGAAAT[C/G]CACCAACCAGCCTGG	84900
rs569048086	snp	A/G	0.000106174	0.00728531	missense, intron-variant	RNFT2	GRCh38.p7	12:116849317	CTGTCCCCGCAGCAC[A/G]TGTTCTGTGAGGAGT	84900
rs569062130	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844361	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	84900
rs569072425	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800995	GCTGATACGTCTAGG[A/T]TTCTCTTCTTGTTTG	84900
rs569112644	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833731	GGGGCGGGGGGCCCC[C/G]CAGCTGGGTCCTTTG	84900
rs569113292	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116768770	AGTTTTGCCCTTGTC[G/T]CCCAGGCTGGAGTGC	84900
rs569116234	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853000	TGTGGGGGACACACA[G/T]GGGCAGATGGGATGG	84900
rs569123241	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814079	TGACCCCAGCCCTCC[C/G]CGTGTCATTCTCCAG	84900
rs569173268	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847443	GGAACTGAGGCACAG[A/G]CAGGTTGCATTACTT	84900
rs569186258	snp	A/G	0.00716266	0.059414	intron-variant	RNFT2	GRCh38.p7	12:116818029	AGAATTCGTTTAGGG[A/G]AACGGGAAAGGGCTT	84900
rs569194735	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799141	TGTGTGATCGTAGGA[A/C]TTGAGGTCCTCCATC	84900
rs569242383	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116767531	CCTGGCCCCGAAAGA[G/T]TGTCATTTCAACATA	84900
rs569251943	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841150	TCTCACAGTTTTTAC[A/G]GGTCAAGAATCCAGG	84900
rs569275055	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116767894	TACATTCTTTTTTCA[C/T]GTTAACTCTTTGTAA	84900
rs569287345	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116810236	GACACCTAAACCAGT[C/T]CCCAGCAGAGACTTC	84900
rs569287959	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116819296	TTCGCAAACTGAGAT[C/T]TCCTTTGTCCGCGAA	84900
rs569288978	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802893	TGAATCCAGGAGTTC[A/G]AACCCAGCCTGGGTG	84900
rs569376820	snp	C/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116794429	GTGGCAAAATCCTGT[C/T]TCTACTAAAAACACA	84900
rs569379818	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116833300	AGGAAGGACACGTAT[C/T]TCCCCGCTTTGGGCC	84900
rs569427961	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809712	AGTCTTGCTCTTGTT[A/G]CTCAGGTTGGAGCAC	84900
rs569489177	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775742	AATATGATTCTTTTA[C/T]GATTAAATATCATAA	84900
rs569515737	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116823295	AGAGAGGGAGAGCAG[C/G]TTGCCCAAAGTCACA	84900
rs569516773	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116830412	CCCACCTCAGCCTCT[C/T]AAGTAGCTGGGACCA	84900
rs569538315	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116763178	GTCTGTGCTTTCAGA[-/A]AAAAAAAAAAAATCT	84900
rs569558219	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116799671	CTGGGCACGATGGCT[C/T]ATGCCTGTAATCCCT	84900
rs569561841	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753796	GTCCCTAAGTCAGAA[G/T]GGCTCAGAATTCCCA	84900
rs569601559	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116816446	GCACCAGAGGCGATC[A/G]CGGCCTCCTCCTCCC	84900
rs569629972	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116770472	TCCCAGTCATTAAGC[G/T]ATGTATGACTGTATT	84900
rs569637055	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764789	CCCAGCCACTTGGGA[A/G]GCTGAGGCAGGAGAA	84900
rs569651256	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116798784	TTTCACCATGTTGCC[A/C]AGGCTGGGCTCGAAC	84900
rs569667951	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116796749	AATCAGACATCTGTC[C/T]ATGCTGGGGCAGGTC	84900
rs569674355	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116757332	TCATTTAGTTCTGCT[C/G]TGATCTTGGTTATTT	84900
rs569695030	in-del	-/TA	0.00478085	0.0486577	intron-variant	RNFT2	GRCh38.p7	12:116756482	ATCATAGATGGCTTT[-/TA]TTACACTAAGGTATG	84900
rs569734886	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116825777	TGTGTGTATTCAACC[C/T]CATTTACAGATGAAG	84900
rs569782273	in-del	-/TCAAG	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116774599	GGACAGGGATGAAAC[-/TCAAG]TCAGCCTTTCAGATC	84900
rs569825842	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116845013	TTTGAGAGGCCAAGG[C/T]GGGAGGATCACATGA	84900
rs569857840	in-del	-/TAGA	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116789911	TGGGTGGATGGATGG[-/TAGA]TGGATGGATGGGAGG	84900
rs569881940	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791821	CATGCTGTAATCCTA[C/T]GTTGAACCTTTTGAG	84900
rs569912838	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795575	CCACGTTTCAAGGGC[C/T]CAAACGCAGAAATGG	84900
rs569915246	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116784524	CTCTTTCATCTGGGG[A/C]CTGGGTTGAACCAGG	84900
rs569926001	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116750362	ACAGGCAGGCTGCCT[A/G]CAGCCGGTGGGGTGG	84900
rs569933112	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761276	GCCTCAGTCTCCCCA[A/G]TAGCTGGGACTACAG	84900
rs569948896	snp	C/T			utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852587	TACCCTGAGGAAAAA[C/T]CAAAGGGAAGCAACA	84900
rs569954653	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116777792	ATTCATGAGAACCCT[G/T]AGGCTTCCAGAGATA	84900
rs569960052	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116758123	TTTAAAGTTTGTTTT[A/G]TCTGATATAAGAATA	84900
rs569999607	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116789767	AATGGGAGGAGAGTG[C/G]ATGGATGGATGGGTA	84900
rs570051786	snp	C/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116741675	TTCTTTTTTGAGAGA[C/G]AGTCTTGCTCTGTTA	84900
rs570053722	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771012	CACCCATCCATTTAC[A/G]TATCATTTATGAGTT	84900
rs570068567	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820130	CAGTCTTACTGTGTC[C/T]CCCAGGCTGGAGTGT	84900
rs570090815	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843197	GACCAGGGGGCAGTT[A/T]ACAATCCAAGGCCAG	84900
rs570113766	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116842666	GCAACCTCTGCCTCC[C/T]GAGTTCAAGCGATTC	84900
rs570137581	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822435	TAGATACTGTCAGAT[C/G]CAGCATTTTCCAGCT	84900
rs570156251	snp	C/T	0.00398564	0.0444627	intron-variant	RNFT2	GRCh38.p7	12:116795133	AATGAAGGCCGGGCC[C/T]GGTGGCTCATGCCTG	84900
rs570169660	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752519	GTTTTATGTGCTTAT[A/G]GTGAAGAAATACAGC	84900
rs570188579	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116767962	CTAACCACATTTCAA[A/G]TGTTCAAAATGGTTA	84900
rs570210606	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116820974	CCCACTCTGTTCTTC[A/C]CTCCCCTGCCTCTGT	84900
rs570240191	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769877	TCTCTACTAAAAAAA[A/G]TACCAAAATTAGCCA	84900
rs570243821	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116753081	GCTGGGATTTTTTTT[A/T]CTCATTGAACATTAA	84900
rs570249737	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737328	GGAAAAAGAGGAGGA[A/C]GGGAAGGAAGGAGGA	84900
rs570282012	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116774295	TGGTTAAGACGGTAC[C/T]TTTTATGTTATGTGT	84900
rs570296676	in-del	-/A	0.00517822	0.0506191	intron-variant	RNFT2	GRCh38.p7	12:116828846	GTAGGGAAGAGTGAC[-/A]AAAGCAGGTTAAGGC	84900
rs570310212	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116785944	GTAGTCCCAGCTACT[C/G]AGGAGGTTGAGGTGG	84900
rs570328001	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828866	CAGGTTAAGGCCAGG[A/C]ATGGTGGCTCACATC	84900
rs570341426	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116746723	TCATCTCTCTGAGCC[G/T]CAGTTTGTTTGTCAG	84900
rs570400427	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781014	CAAAGTACTCACTTT[C/G]TAAGAACTATTGGTT	84900
rs570408213	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736543	CTAAATGTAGAGTGA[C/G]CACATAGTTTTATCA	84900
rs570440792	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839167	TTCCAATTGTTAACT[A/G]GGTAGTTCATTTGGT	84900
rs570446325	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746561	ATCTGACAGATGAGC[A/G]TGCATTACCTAGTTG	84900
rs570455321	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116850753	CTGCCTCAGCCTCCC[A/G]AGTAGTTGGGACAAC	84900
rs570473915	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792390	GGAGAAAAGTCCTCC[C/T]AAACCATTCACATAA	84900
rs570498008	snp	C/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116745839	GGTGCATTGTGCCGG[C/G]TGGTAAAGATACAGT	84900
rs570500323	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116819338	CTCAGGCTCGGGGGC[C/T]TGGTACCGGCGCGGG	84900
rs570503193	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847077	CCATGCCTGGCTAAT[G/T]TTTGTATTTTTAGTA	84900
rs570565121	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798993	GTCAGCAGTCCAGGT[C/T]AGCTTGATTGAGTTT	84900
rs570578619	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823221	TGTTTTAACAGTGCA[C/T]AGAGGCCCAGAATGG	84900
rs570639783	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116758304	TTTAAGTGGAGCATT[C/T]AGGCCACTTACATTC	84900
rs570682843	snp	A/C	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116819381	CAGACCCGGAGCCGG[A/C]GGCGCGCAGAGCGGG	84900
rs570683666	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739413	GGGTGATCCAAGTAG[A/G]CAGGATCCCTACTTT	84900
rs570700661	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739696	TAGAGGAACAGAAGG[A/G]CCACTGTGGGTGGAC	84900
rs570726664	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116742265	GTACCGAGGTGGTTT[-/C]TTTTTTTTTTTTTTT	84900
rs570732146	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759811	TTAGCTTTGGTGGTT[C/T]AATGCGCTATTTTTG	84900
rs570765878	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116772219	ACCTCAGCCTCCCAA[A/G]GTGCTGGGAATACTG	84900
rs570798988	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851640	AGCTACTCAGGAGGC[C/T]AAGGCAGGGAGAACT	84900
rs570828751	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116816472	CTCCCCCTCCTCGCC[A/G]GAAGAGCAGAGAGAG	84900
rs570850093	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764363	AATAATTTTTTTTTT[A/G]AAGTCTGTGCTTTCT	84900
rs570858439	snp	G/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116846774	TTGACATCAATTTTT[G/T]TTTCCCTAAACCAGT	84900
rs570893524	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814114	AGATGATGATAGTCA[C/T]TGTCATGGCAACATT	84900
rs570965248	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116793847	CCTAGCATATACCAG[C/T]ATCTGAAATAATCAG	84900
rs570980057	in-del	-/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116846631	AACATTTTGTTTAGA[-/T]TTTTTTTATTATTAT	84900
rs570980854	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846596	TGCCCAGTTTCTTTT[C/T]TGTGGTTTTGCTTTT	84900
rs570981994	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820642	CCCACATCTTACTTT[A/G]TCTCCTAAGGTCTCC	84900
rs570982115	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828130	CAAGATGGCGCTCAG[A/G]CCAGTGACCATCTTT	84900
rs570987445	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116825880	AATCCCAAATCCCAC[A/G]CCTTTAAACCACTAG	84900
rs571011180	snp	A/C	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116811196	GATGGCTTGAGCCCA[A/C]GAGTTCAAGTCCAGG	84900
rs571043945	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821079	TGGCCCCTGGTAAGC[A/G]CTTAATACGGGGGTT	84900
rs571077102	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741950	ACCACTGCACCTGGC[A/G]TGGGTTAGGTTTCAA	84900
rs571081693	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818545	TGGGAGAAATCTGCT[G/T]CTGGCAAGTGAGTTG	84900
rs571090864	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798446	TGTGTTCAAATCCTG[C/T]TTGAGAAACCCTCTG	84900
rs571132690	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843263	TTTGGGAGGCTGAGG[C/T]GATTGGATCCCTTGA	84900
rs571156800	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116766600	TGCCTTTCTAGATAG[C/T]TTTTCAAGCAGATGT	84900
rs571190884	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831620	TGATTATTTTGTTAG[A/G]GTAAATTGCCAGACA	84900
rs571206253	snp	A/G	0.000307393	0.0123936	missense, intron-variant	RNFT2	GRCh38.p7	12:116849360	GGCTGGACCGTGAGC[A/G]CACCTGCCCGCTCTG	84900
rs571222876	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741573	TCTCCTTTTTAAGGG[C/T]ACTAATCCCATTCGT	84900
rs571231635	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116776536	TCCATGGAGACAGGG[A/C]AGGGATGTGGGAGGG	84900
rs571237104	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782431	ATTTGGGAGCCCAAG[A/C]TGGGAGGATTGCTTG	84900
rs571299297	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803561	ATCAGGGTATCCCAG[A/G]TGCTGCTGTCAACAA	84900
rs571346229	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116775863	GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	84900
rs571349386	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800169	CTACAGTCTGCAGAA[A/C]CATGAGCCAAGATAA	84900
rs571406007	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815434	ACTGTGGTTCCTTTG[C/G]GAGGCTCCGGGGGAC	84900
rs571448982	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116801908	CTCATTGCCACCTCC[A/G]CCTCCCAGGTTCAAG	84900
rs571474302	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808721	AATTCATTTTCTATT[A/G]AACCAAATGATACTG	84900
rs571483067	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116763772	TGACAGAGCGAGACT[C/T]CATCTCAAAAAAAAA	84900
rs571497951	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795719	TAGCAGATGGAGAAA[C/T]ATAAAAGCGGGCCCT	84900
rs571510387	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116802710	GGAAACTAATTTTGG[A/G]CTTCTGGCCTCCAGA	84900
rs571529798	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807896	ACAGCCTCAAACTCC[A/T]GGGCTCAAACGATCC	84900
rs571559305	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769723	AATTTATGATTGAAG[A/T]AATAAACATTTTAAA	84900
rs571573328	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762208	ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAAGA	84900
rs571577254	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841328	TGTGGTGGTGCACGC[C/T]TGTGGTCCCAGCTAC	84900
rs571585605	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116794078	CGAGACCAGCCTGGC[A/C]ACAAAGTGAGACCCT	84900
rs571629097	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848066	GTGTTCTCATTGTTC[A/G]GCTCTGATTTATGAG	84900
rs571660770	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775662	GGCTAGTTAGGAAGG[C/T]CACATGTCATAAGAC	84900
rs571692277	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848515	ACAAGTACCTACACC[A/G]TATGCACCCCTCACC	84900
rs571729894	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749714	GGGAGGAAGGACTTC[A/G]TGTGAATTTGAGGGG	84900
rs571776044	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116796100	TTTTAGTAGAGAAGG[G/T]TTTTCACCATTTTGG	84900
rs571793570	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788655	TGAATGCATCCAGTT[G/T]GTTTGTTGATGGATC	84900
rs571810488	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116755794	TCACATATACATGGC[C/T]AAAGGAACAACTCCA	84900
rs571894879	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116840664	AACAATATCCTAGGC[A/C]CTAACTCTGTAACCC	84900
rs571903463	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837141	CTGGCCGGTTCCTTT[G/T]AAATCCCTAAATGCA	84900
rs571908930	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116829197	GATATTCTGCAGATC[A/T]TGGGGTCTGCAGCAG	84900
rs571914028	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782003	AGAATTGCTTAAACC[C/T]GGGAGGCGGAGGTTG	84900
rs571920909	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817497	TGTTATTAAAGGTGA[C/G]AGCATAAGCTGTATA	84900
rs571928306	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747548	GTGGATAATGGTCTC[A/G]TATAATAGATGATAT	84900
rs571940112	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790879	GGAGGATCACTTAAG[C/G]CTAATAAGGTTAAGG	84900
rs571954286	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834553	ATTAAGCAGTCACTC[A/C]CCATTCTTCCAACCT	84900
rs572027501	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116837799	TTAGCTTTGACAAAT[A/G]TACCACGGTAATGCA	84900
rs572052625	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116776079	TTATTGGTGGAGGTG[C/T]CTAAGGAGGAGCAAA	84900
rs572057881	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116823291	GCCCAGAGAGGGAGA[A/G]CAGCTTGCCCAAAGT	84900
rs572064393	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116802990	GACCCAGCTACTCAG[G/T]AGGCTGAGGTGGGAG	84900
rs572103845	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836522	TAGAATGCCAAATTC[C/T]GTATGGTGTAACATC	84900
rs572111237	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790342	TCTGAGGATACATCA[A/G]TGAACCAGTAAATAG	84900
rs572154873	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116769411	CATTGCTATCGTAGG[A/G]GATTACAGCTCCATG	84900
rs572167756	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116844471	TCAACTCCTGACCTC[A/G]TGATCTGCCCACCTT	84900
rs572271116	in-del	-/G	0.0501905	0.150254	intron-variant	RNFT2	GRCh38.p7	12:116752198	CTACTGAAAAAAAAA[-/G]AGAGAGAGAGAAAGC	84900
rs572285870	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830526	CTCCTGGGCTCAAGG[A/G]ATCCTCCCACCTTAG	84900
rs572311125	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771626	GATAAAAATGTCTAC[C/T]CCATCTGGGTTGAGC	84900
rs572344765	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738010	CCTCCAGGCAGGCGC[C/T]GGCCCCGCCGCCCGC	84900
rs572376206	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116834079	GAGGGAAAATTCATA[C/T]GACATGAAATTAACC	84900
rs572383777	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736655	CAACAGCATAACCCA[A/T]TATCCTGGGTGCACC	84900
rs572403166	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741876	GACTGGCCTCAAACT[C/T]CTGGGCTCAAGCGAT	84900
rs572412005	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814988	TGACCCGCCTGCGTC[A/G]GCCTCCCAAAGTGCT	84900
rs572469096	snp	A/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116782762	TTCTCACATGCCGAA[A/T]ATAAGTCTGAACACA	84900
rs572478441	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116822009	CAGCTAATTTTTTGT[A/G]TTTTTGGTAGAGACG	84900
rs572519922	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116763950	AAAATGTAGAACCAT[C/T]CCAAATGCCCATCAA	84900
rs572554089	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739023	AAGAGAAAGGAGGCT[G/T]CACTGGCGGGTCATT	84900
rs572590128	in-del	-/A/AA			intron-variant	RNFT2	GRCh38.p7	12:116802932	AACTCTGTCTCTACC[-/A/AA]AAAAAAAAAAAAATT	84900
rs572593981	snp	C/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116809795	CTCCTGCCTCAGCCT[C/G]CTGAGTAGCTGGGAC	84900
rs572612066	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116785353	GCTGGAGTACAGAGG[C/T]GCAATCACAGTTCAC	84900
rs572612686	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116764587	TGCAAACTCCTTTCT[C/G]CTGTTGTTAAAACAG	84900
rs572620352	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116815836	AGAGAAGTGATTGAT[A/G]TGACTTCGGCAAAGT	84900
rs572623004	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782034	CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA	84900
rs572629472	in-del	-/TGGAGTGCA			intron-variant	RNFT2	GRCh38.p7	12:116821863	CTCTGTCGCCCAGGC[-/TGGAGTGCA]TGGAGTGCATGGAGT	84900
rs572645357	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116797863	AAATTTCCAGGGAAG[G/T]GGTAGTCACTTTTGG	84900
rs572670424	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808994	CCTTTTAGGATGGCC[A/G]CCCCATCCCAAGGCC	84900
rs572684295	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763585	CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	84900
rs572703608	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781055	CAGAGTGCTTTGCTC[A/C]ACGCTCTGCACATAG	84900
rs572711648	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116850736	GGGTTCAAGTGATTC[A/T]CCTGCCTCAGCCTCC	84900
rs572738465	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116749755	AACCCATAACATAAT[C/T]GATATTATTAGTCCC	84900
rs572772648	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823737	ACTGCCATCCTCTTT[A/G]ACCAGACTTAATTTA	84900
rs572857062	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116845456	GGGGCAACATCATAA[A/G]ACAGGGGAGACATGA	84900
rs572885353	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812052	CTCCAGGAGGAGCCC[A/G]GTGAGGAACAAATGA	84900
rs572896897	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116826250	ATTGTCCCACCCCTC[A/T]TCTTGGCAGTGAGGA	84900
rs572912991	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780575	ACCCCTGGTTTCTAG[C/T]TGAGCCAAAATCCTA	84900
rs572922191	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116827920	ATCCCAGCCTCTTTG[G/T]TTCCTGGGGCTGTGC	84900
rs572950567	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807401	CAGTGTCCCTAGTAC[C/T]GGTCTAAATGCTTCA	84900
rs572955768	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116760972	TAGCCTCCAACTCCC[A/G]GATTCAAGCAATCCT	84900
rs572971533	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818125	AATATTTACCAGCCT[A/G]GGCAACACAGGGGAG	84900
rs573017936	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822866	GCCAGCCATGGTGGT[A/G]CACGCCTATAATCCC	84900
rs573029267	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116847574	CTCTCGTTGCCCAGG[A/C]TGGAACACAATGGCA	84900
rs573058216	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116839352	ATGGATGGGATGGTT[A/G]GATGGAATGTTTAGA	84900
rs573089430	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116784936	TCTCCTATCACTTCC[C/T]CTCACCTTCACCCAA	84900
rs573092755	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116848092	ATGAGTGAGAACATG[G/T]GGTGTTTGGTTTTCT	84900
rs573115028	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116745948	TAGAATCACTGTAGC[A/G]GGGGGCAGTGGGGAA	84900
rs573125952	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806899	TTATTCTTTGAATGT[A/G]CTTCTGGATTCCGTG	84900
rs573136638	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763143	ATGTAGGAAACATTT[A/G]ATTGAGCTAGTTTTC	84900
rs573160366	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116851670	TGCTTGAACTCGGGA[A/G]GTGAAAGTTGCAGTG	84900
rs573201365	snp	C/T	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116759055	CTTTGTTCATATTTT[C/T]TTATTCCCTTTTCTT	84900
rs573229616	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116810818	CTGCTTTTTGCTTCC[A/G]TTGGGGTAGGGGGGA	84900
rs573233705	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116765129	AGCTTAGGCGTCGCA[C/G]CTGATTAGGAGAGAA	84900
rs573290582	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804317	CCTCAGACCCCACCC[C/G]AGACCTACTGATTCA	84900
rs573314869	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831767	CATGTTAGGAGTGTA[C/T]ATTTCAATGAGTTTT	84900
rs573317598	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842807	ACAAACTCCTGGCCT[A/C]AAGTGATCCACCCAC	84900
rs573319998	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811438	TGGAGTGCAGTGGGG[C/T]CATCTCGGCTCACTG	84900
rs573374673	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116814804	ATGCTTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	84900
rs573405961	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116832631	CTTTATTAGACACTA[C/T]AGAGTGGGTGTATTT	84900
rs573466542	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792466	GAAACGGACACTGCT[A/G]GGGCCGAGGAGGCGG	84900
rs573544189	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798045	TGAGCCCCATCTCTG[A/G]AGTCAAGTCCCGCCT	84900
rs573555833	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116801361	TTTCTGTTGCCAGGA[A/T]GATTCTAGAGCATGT	84900
rs573558325	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755913	CAGTTCCGGCTGAAA[A/G]GAAAAGATATGTCCT	84900
rs573579628	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116843316	TGGCCAACATAGCAA[G/T]ACCCCAACTCTACAA	84900
rs573579738	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835888	AGGGTCAGAGGATGG[A/G]GTGGGGTGATTGTGC	84900
rs573582930	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116792161	TTCAAGCAATTCTCC[C/T]GACTCAGCCTCCTGA	84900
rs573634133	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116741952	CACTGCACCTGGCAT[A/G]GGTTAGGTTTCAACA	84900
rs573640641	snp	A/G	0.000163693	0.00904542	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836300	GAGCAGGGCTCAGGC[A/G]GGACCATTGGAGACC	84900
rs573653779	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808157	GTTGTAGAGATGGGG[A/G]TTTCACCATGTTGGC	84900
rs573691458	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116808772	GCAGGGAGGAGGGGC[A/G]GTCAGGCCTCCTCCT	84900
rs573754482	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116762726	AAGTGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA	84900
rs573756682	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116769320	CCGTGATCACGCCAC[C/T]GCACTCCAGACAGAG	84900
rs573758532	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829102	GTTGAGAGACCATGG[A/G]TGAGAGCAATTTGGG	84900
rs573761576	snp	A/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116793237	TTTTTTTTGAGGCAG[A/G]GTTTCATTGTCCAGG	84900
rs573770128	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782894	CCCCAAACCCTGCCC[A/G]CACCTTTGTAAATAG	84900
rs573804158	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116756517	CTTGTATGCCATTTT[G/T]CTGAGAGTTTTAATC	84900
rs573815680	in-del	-/GG	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116844939	AACCAGGTTCTGCCC[-/GG]TCAGAAAGCTCTCAA	84900
rs573843523	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116749101	AAGTACCACACCCCA[A/G]GGGGCTTAAACAACA	84900
rs573903746	in-del	-/ATT	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116846733	CCAGATTTACTGATC[-/ATT]AACATTTTACATTTG	84900
rs573905465	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749717	AGGAAGGACTTCATG[A/T]GAATTTGAGGGGGAC	84900
rs573921309	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116828428	AGACTTTGTTGATCA[A/G]TTTCCCCTCCACATC	84900
rs573945102	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795323	TGAGTCAGAAGAATC[A/G]CTTGAACCCAGGAGG	84900
rs573977072	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116837953	TCTTTGAAAGATATA[A/T]AAAGGAGGCCTGTCA	84900
rs573983851	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116789123	TGGAAGGAGAGTGGA[C/T]GGGTGGATGGGTAAA	84900
rs574010769	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799860	TTTGGATGTTTGTCC[C/G]CTCCAAATCTCATGG	84900
rs574041230	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820761	AGCAACTTCGAACAA[C/T]ATACCCTGCCTCTTT	84900
rs574106812	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116776043	GCGAGACTCTCAAAA[A/G]AAAAACAAAAAAACT	84900
rs574116216	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803856	GGAAACTGGAGAATT[A/G]CATGAAAGGTTTTTG	84900
rs574129690	in-del	-/AAAA			intron-variant	RNFT2	GRCh38.p7	12:116775276	CAAAAAAAAAAAAAA[-/AAAA]GAGAGAGAGAAGAGC	84900
rs574158188	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790999	AAATAAACCATTAAT[C/G]ATTTTAGAGTATGCC	84900
rs574162417	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116841405	CTGCAGTGAGCCGAG[A/G]TTGCACCACTACACC	84900
rs574180494	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116747010	GACTCAAGGTTGGTT[A/G]AATCCTTAAATACAG	84900
rs574196623	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791625	TTCATTCCTTCTTAT[A/G]GCTAAATAATATTCC	84900
rs574235518	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827786	GCTGCCCAATAGCAA[A/G]TGGGAAGTTTGGGAT	84900
rs574269014	snp	G/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116782056	TGCACTCCAGCTTGG[G/T]CGACAGAGCGAGACT	84900
rs574283717	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811509	GTCTCCTGAGCAGCT[G/T]GGATTACAGGCGCCC	84900
rs574288282	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775309	CAACATAGCTGAGTC[C/T]TTGTCCTTACTGAAG	84900
rs574304978	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116830504	TATTGCCCAGGCTGG[A/T]CTTGAACTCCTGGGC	84900
rs574321662	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768930	GAGAAAGTGTTTTGC[C/T]ATATTGGCCAGGCTG	84900
rs574334048	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116740941	AGGGGTCTAAGATAC[A/G]ACTAGTGCAGGTTTG	84900
rs574353620	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116817539	TCCACGCCTAATTTC[C/T]TACTCAGTTCCTCTG	84900
rs574370348	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116804451	GCTCTAGTTCTCAGT[C/T]TATTCATTTTTCAGC	84900
rs574377628	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779252	TGACCTGCTATGGAT[C/T]GTGGGGATCGCAGAC	84900
rs574389835	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778818	TCATGCCACTGCACT[C/T]CAGCCTGGGAGACGG	84900
rs574437863	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797424	AATTAGCCAGGTTTG[C/G]TGGCGTGTGCCTGTA	84900
rs574441214	snp	A/C	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116814823	AGCTGGGATTACAGG[A/C]ATGCACCACCATGCC	84900
rs574447653	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116770101	TCTACAGCAGTGTAT[A/G]GTCATGTCCTAGGCC	84900
rs574465247	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116751371	TATCTGACACATACT[C/T]AACAGTCAATAATTG	84900
rs574490995	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116831565	ATTACAAAGAATGCT[A/G]TAGTGACCATTCCTA	84900
rs574507706	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738031	CGCCGCCCGCAGCCC[A/C]GTCTGCTCCCGGCAG	84900
rs574535702	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116763998	AAACTGGTATATGTA[C/T]ATGATGGAATTCTAC	84900
rs574535770	snp	A/G	0.00676609	0.0577691	intron-variant	RNFT2	GRCh38.p7	12:116770703	GCTGGGACTTCAGGC[A/G]CATGTTACCATGCTC	84900
rs574554125	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736780	CTCCTTGCTGTTTCT[A/C]CCAGAAATTCTCACA	84900
rs574564385	snp	G/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116837987	TATGTATGTATATGT[G/T]TGTATATATTTATAC	84900
rs574577863	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116792067	AATTTTCTTTTTTGT[A/T]TTTTGAGACAGAGTC	84900
rs574582925	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116743353	CTCACTACAACTTCC[A/G]CCTCCTGGGTTCAAG	84900
rs574619904	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743889	ATGACTTCACCCCTA[A/G]GTCTCAGCTTCTCCA	84900
rs574628291	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116830637	GGGCTGGGCGCGGTC[A/G]CTCACACCTGTAATT	84900
rs574661157	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771741	GACTCAGAGTTCTAC[A/G]CAATGTGGTGGGGCA	84900
rs574690560	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116779935	CAGGGCTCAGACAAG[G/T]TATCACCTGTAGGAC	84900
rs574702561	snp	A/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116818167	ACAAAAAAAGTCTTT[A/T]AAAAATTATCTGGGG	84900
rs574708092	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784852	TGTGTGTCCACTCCA[A/G]CCCCCTCCACTTCAT	84900
rs574726681	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116778187	CTGTTGTGGACCCAC[A/G]AAACTAGAGGGGACT	84900
rs574746025	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738384	AGGTAAAAAGAGAAC[A/G]CGATTTTTTTTTCTT	84900
rs574750350	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763089	CTTCTCTGTTTAAGA[A/G]AAAATAAAAAGAAGG	84900
rs574764236	snp	A/G	0.000123801	0.0078667	intron-variant	RNFT2	GRCh38.p7	12:116849270	GAGACCGAGGCAGAC[A/G]CTCAGTAAAGAGTCC	84900
rs574769170	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809382	TCGGCAACTCCTTCA[C/T]GTGGCCTGGGGGGTC	84900
rs574803941	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116822035	AGACGGGATTTCACC[A/G]TGTTGGCCAGGCTGA	84900
rs574812810	in-del	-/AAGAC	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737673	AAGGGAAGGGGTAGG[-/AAGAC]AAGACAGGGAGGAAG	84900
rs574817990	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116766030	TAATTCCAGTGTTTT[C/G]GGAGCCCAAGGCAGG	84900
rs574873611	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809503	CAGGTAAAGAGCACT[C/T]TGATATGCAACCAGC	84900
rs574875607	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816499	AGAGGATCTTTATAG[A/G]AAATTGGGGGTGAGA	84900
rs574925512	in-del	-/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116813122	ACCATGCCTGGCTAA[-/T]TTTTTTTTGTATTTT	84900
rs574994823	snp	A/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116845337	GAATTTGCAAATAAT[A/T]CCTCATGCAATGCTT	84900
rs575044940	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116803051	AGTGAGCCGAGATCA[C/T]GCCACTGCACCCCAG	84900
rs575064973	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754147	CGGCAAGTCTCCAGA[A/G]TTCATTGTATCATTC	84900
rs575082161	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116775037	GAGGCTGAGGTGGGC[A/G]GATCCCCTGAGGTCA	84900
rs575102760	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116754777	TTGTTGGCCATTTGT[A/G]TATCTTCTTTTGAAA	84900
rs575131098	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116787453	TGGCTCACACCTGTA[A/T]TCCCTGTTTTGGGAG	84900
rs575137631	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116809846	CTCAGCTAATTTTTT[A/G]TATTTTTTAGTAAAG	84900
rs575172748	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768183	CCGGCTCACTGCAAC[C/T]TATGCCTCCCAGGTT	84900
rs575175691	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116761513	GCTGCTGGGTGGACA[C/T]AGAGCTTCACCACCA	84900
rs575296209	snp	A/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848623	TCCTCCCGCACATCA[A/T]ACACAGTCCAGCCTC	84900
rs575301436	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813341	GCCAAGTGTTTTGAA[C/T]GCCTCTTAGGGCTGA	84900
rs575301708	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116806981	GTTCCTCTCCCTTTT[G/T]ACATGGCTTCCCGGA	84900
rs575322715	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116800295	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	84900
rs575345937	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116749308	CCCTTTTGAGACAGG[A/C]TCTCTGTCGCCCAGG	84900
rs575347746	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116841446	TGACAGAGGGAGACC[C/T]TGTCTCAAAAAAATA	84900
rs575362316	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842061	TCAAGGTATTACCAG[A/G]GCTGTGGTCCTCTCC	84900
rs575374562	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811985	GGTGAGTGAGTTCAC[C/T]GGGTCAAACTCTGAT	84900
rs575384781	snp	A/G	0.0103295	0.0711199	intron-variant	RNFT2	GRCh38.p7	12:116794547	AGGCTGCAGTGAGCC[A/G]AGATTGTGCCACTGC	84900
rs575393836	snp	C/T	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116794178	GCTGAGGTGGGAAGA[C/T]TGCTTGAGCCAAGCA	84900
rs575437590	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116812670	CTCCTGAGTAGCTGC[A/G]ATTACAGCATGCGCC	84900
rs575483237	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848210	CATAGTATTCCATGG[C/T]GTATATGTACCACAT	84900
rs575509133	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116832843	AACTAAGGGTCATGA[A/G]CATCCAGCAAGGTCA	84900
rs575509649	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116799912	TGGAGGTGGCGCTTA[A/G]TAGGAGTTGTTTGGG	84900
rs575546382	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116846803	GTTAAGAGTAAGTGG[C/T]AGACATTTAGATTCT	84900
rs575561354	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116807462	ATCCTATGAGGTAGA[C/T]ACTCTTAATGCCCCC	84900
rs575570555	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116833216	GAGCCACCACACCCG[A/G]CCCCTGTTCTTTCTC	84900
rs575572136	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116833360	CCCATCCTGCCCAGG[A/C]CCCTGAGAGCAGTCG	84900
rs575593540	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116798680	CTGAAGTGATTCTCC[C/T]GCCTCAGCCTCCTGA	84900
rs575610366	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116791825	CTGTAATCCTATGTT[A/G]AACCTTTTGAGGAAC	84900
rs575629926	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116771705	ATGTCCCATGATGTG[C/G]GCACCCTCTTCTGTG	84900
rs575632202	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792546	TATTAATGCCTCCCT[A/G]GCAACTGTCCAGCTC	84900
rs575639406	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116846314	GTCTCACTCTGTCTC[C/G]CAGGCTGGAGTGAAG	84900
rs575646238	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836401	AATCCGGTTAAGACC[A/G]GAGTCAGCCAGACCT	84900
rs575691080	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852458	GTAGCATCTTTCAAG[C/T]TCCGTTACTATGGCG	84900
rs575787105	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116759282	TATCATATTTTGGAA[C/T]TCGTTGCACTGGGCT	84900
rs575866489	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116780619	TTCTTAGATGAAGCC[A/G]CAGCTCTGGTACCCA	84900
rs575868411	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116786612	TCCAGCTCTTCCAAG[G/T]CTCTCAATACCCCTG	84900
rs575873324	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792917	TTTGCTATTTGGGTC[A/G]GTTGATGGCCCTGAC	84900
rs575875278	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116759313	TTGCCTTTCTCTGGT[C/G]CCTCCCTGATTAGCT	84900
rs575881872	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116746763	TGATATTTGGGAATG[A/G]TATTTGTACCTGTCT	84900
rs575885923	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116825811	CTGAGGGTCATAGAG[G/T]TTGAATTATTGTGCC	84900
rs575945336	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795992	CGGCTCACTGAAACC[C/T]CTGCCTCCCGGGTTC	84900
rs575954191	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749940	ACCAGCGCTCTTCTC[A/G]GGCTTATCAGGCAGC	84900
rs575956851	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797660	AGAATTCAAGGGTGA[A/G]CCAGTGGTAGGGTAG	84900
rs575957266	snp	A/G	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116781174	GAATTACTTAGCCTC[A/G]GTGCCCTCATCTGTA	84900
rs575963969	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736850	GAATTCTACCAATCA[A/G]GTTATGCACAAAAAG	84900
rs575971972	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116829815	TGAACTCCTGGCCTC[A/G]AGAGATCTGTCCACC	84900
rs575986921	snp	C/T	0.00835141	0.0640778	intron-variant	RNFT2	GRCh38.p7	12:116798777	GACGGGGTTTCACCA[C/T]GTTGCCCAGGCTGGG	84900
rs575988148	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116790198	GAAAGAAATCTGGCA[C/G]CCACACTTATAATAA	84900
rs576015151	snp	A/C	0.00279162	0.0372561	intron-variant	RNFT2	GRCh38.p7	12:116821418	GCCCTTCAAGCCTCC[A/C]GGTCGGTGCTGGGTC	84900
rs576055532	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116850113	GCCTCACGAAGTGCT[A/G]GGATTACAGGCATGA	84900
rs576075354	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116782693	ACACTCAGTAACCCA[A/C]TGAATCTCTACAACA	84900
rs576086420	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116842878	TGTGCCCGGCGTGTT[C/T]ATACTTTATAAGGGG	84900
rs576096732	snp	A/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116795420	CTCCAGAAAAAAAAA[A/G]AAAGAAAGAAGAAAG	84900
rs576133822	in-del	-/TTTGTT	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116751750	CTGTTTTTTTGTTTG[-/TTTGTT]TTTGTTTTTGTTTTT	84900
rs576151774	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116788021	CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT	84900
rs576200828	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116756011	TGTGATGCCTCCAGC[C/T]TTTTCTTTTTGCTTA	84900
rs576218161	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116745290	AGCGATTCTCCTGCC[A/G]CAGCCTCCTGAGTAG	84900
rs576263440	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116836938	ACATCTCAAAGAAAA[A/C]AAAAAGGACATAATA	84900
rs576316722	snp	A/C	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116743072	GGCAACAGAGTGAGA[A/C]CCTATCTCAAAAAAA	84900
rs576323167	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116831484	GTATGGCTTTCCATT[A/G]TAGATCTCTAACATA	84900
rs576354578	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116778262	ATCCCCAATGATGTT[A/G]GGAGGTGGGGCCTAG	84900
rs576356410	in-del	-/T	0.0197687	0.0974348	intron-variant	RNFT2	GRCh38.p7	12:116798561	CCTATCTGCATTAGG[-/T]TTTTTTTTATTTTTA	84900
rs576428489	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116783564	AGCCACCTGCAGGCA[C/T]AAGGCACATCATCCT	84900
rs576479474	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116780482	CAGGCGGTAATGCTT[A/G]CTCACCCACTGCTCA	84900
rs576484361	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739975	CTTTGGGAGGCCAAG[A/G]CAGGCGGATCACTTG	84900
rs576506614	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116828257	CAAACTTGGATGTGC[A/G]CTCGGGTCACCTGGG	84900
rs576519753	in-del	-/TCCTTTCTTCCT	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116778132	CTTTCTTTTCTTCCC[-/TCCTTTCTTCCT]TCCTTCCTTTTGCCT	84900
rs576628178	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116821285	CCCCAGTCCTGCCCC[A/G]TCACACTTGTTTCTC	84900
rs576649409	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116827873	AGTGACCAAAACTAA[A/G]CCTAAGGTGGCAAGT	84900
rs576694203	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116814937	AATGGGGTTTCACTA[C/T]GTTAGCCAGGCCGGT	84900
rs576707935	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116773319	CTATATTAAGAAAAC[A/G]TATCAACTAAGGGCC	84900
rs576771232	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116818228	CTCGTGGGGCTGAGA[C/G]GGGAGGCTCGCTTGA	84900
rs576797356	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848412	TCGCTTTAAACTGCA[A/G]ATCATATCAGGTCAC	84900
rs576807384	in-del	-/A	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737490	AGGGGAGGAAAGAAG[-/A]AAAGGGAAGGGGGAG	84900
rs576818649	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738044	CCAGTCTGCTCCCGG[A/C]AGCCTTGGGCGCAGC	84900
rs576828025	snp	C/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116744957	CTGCCAGGGCTCTTG[C/G]TTTCTGAGCTGAGCT	84900
rs576835270	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116757755	ATCATATAGTCTATC[C/T]TGGAGAAAGTTCCAT	84900
rs576913026	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738481	GTTGCAGGGATGAAA[A/G]GCGCTCGCGACGTTG	84900
rs576929360	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116838460	CAGTTTTGACAGTTA[G/T]TGCTAAACTGCCCTC	84900
rs576939228	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116767150	ACTAAACAGAAACAG[A/G]TGGAATCAATTATAA	84900
rs576957497	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116744923	AGAGAGTGGCCTCCT[C/G]ATGGACCAACATGGG	84900
rs576997197	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116831693	GGATGCTTGGGGCAG[C/T]GTTGTTTGTTTGATT	84900
rs577028036	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT2	GRCh38.p7	12:116769307	AGGTTGCAGTGAGCC[A/G]TGATCACGCCACTGC	84900
rs577038020	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759419	TAGTGTGATTTTGGG[A/G]GAGTGTTGAAGAGCC	84900
rs577050269	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116794674	GAAGGGAGGAAGGAA[-/G]GGAGGGAGGGAGGGA	84900
rs577058972	snp	A/C	0.0158469	0.0875917	intron-variant	RNFT2	GRCh38.p7	12:116824567	GATGGTAGCAAGAGC[A/C]CCAGCCATCACATCC	84900
rs577097118	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771284	GGGCAACATGGTGAG[A/G]CTCCATCTCTACAAA	84900
rs577097484	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116811968	CTAGCTATATACCCT[C/T]GGGTGAGTGAGTTCA	84900
rs577138878	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116771409	AGGCTGCAGTGAGCC[A/G]TAATCACACCACTGC	84900
rs577160511	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116810603	CTGACCCACCTTTCC[A/G]AACTACATCATGGGT	84900
rs577160821	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116764866	CACTACACTCCAGCC[C/T]GGGCAACAAGAGCGA	84900
rs577187941	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116848304	TAGTGCTGCAGTGAA[C/T]GTATGCGTGCATGTA	84900
rs577202581	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116787591	CATGGTGGAACGCAC[C/G]TGTAGTCCCAGCCAA	84900
rs577227848	snp	G/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116754308	TTAATTCATTCCTTT[G/T]TATGGCTGTGTAGCA	84900
rs577233542	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116816662	CTGAGCTCTATAAGC[A/C/T]TAGGCAAAATGGTGA	84900
rs577249469	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116770759	AGATGAGGTTTCTCC[A/G]TGTTGCCCAGGCTGG	84900
rs577294701	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763672	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	84900
rs577323968	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	RNFT2	GRCh38.p7	12:116854098	AAAGGGATCAGAAAG[C/G]GCCTCTGTGGGGCAC	84900
rs577362967	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116791690	CCTCTGTCAATGGAC[A/G]TCTAGGCTGTTTTTG	84900
rs577393020	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116838581	CTTTTGAGCTTTGCC[A/G]ATCTGACAGGTGACA	84900
rs577399866	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792025	ACCGCGGTCCTTCCC[A/G]TGTATGTTCCCTGAA	84900
rs577402218	snp	C/T	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116796681	TCCCATTGTTGGAGG[C/T]ATCTTCGCTCCTGGA	84900
rs577437026	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116749010	GAAGACTATCTGACA[C/T]GTAGTAGGTTTCAAT	84900
rs577466190	snp	A/G	0.00358779	0.0422022	intron-variant	RNFT2	GRCh38.p7	12:116765181	TTCTGTCTTCCCAGA[A/G]CATTGCTAATTCCCT	84900
rs577475524	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116797470	AGACTGAGGCAGGAG[A/G]CTCACTTGAACCCGG	84900
rs577513476	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116754933	TTCTCCCACTCTGTG[A/G]GTTGTCTGTTTACTC	84900
rs577541689	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116768840	GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC	84900
rs577548717	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116755678	GCATGCTGGGTAACA[C/T]TGTAGACTCTTCCAG	84900
rs577550642	snp	A/G	0.00557542	0.0525036	intron-variant	RNFT2	GRCh38.p7	12:116748311	TGCAGGCCTAACTCC[A/G]GGCTCTCTGCTCCGC	84900
rs577567386	snp	G/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116804240	GTGTGTATTCTTGCT[G/T]CTCAAAGTGCAGTCC	84900
rs577639375	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116813450	CCATCTGGCTGACCC[C/T]TCATCACCCCATCAC	84900
rs577671634	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116798765	TTTTTTGGTAGAGAC[A/G]GGGTTTCACCATGTT	84900
rs577723841	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116834936	CTCATTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	84900
rs577733460	snp	C/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116799204	CCTAGAAGCCACGCT[C/T]CAGTCCTTGTACACA	84900
rs577761381	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116788170	AACCTCAGGTGATCC[A/G]CCTGCTTTGGCCTCC	84900
rs577783490	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT2	GRCh38.p7	12:116741206	TAGTTGTTAGAGTCA[C/T]ACTGATGGCCTCATA	84900
rs577785148	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116835763	GCCTAGGTAGCAGGG[A/G]AAACTCTTGATATTA	84900
rs577795082	snp	A/G	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116788862	GATAAATGGGAGGAG[A/G]GTGGATGGATGAATG	84900
rs577824164	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116820096	GGATATTGTTTGTTT[A/G]TTTGTTTGTTTTTAA	84900
rs577859108	in-del	-/AAA	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116829920	TCACATGCTCAGTAT[-/AAA]AAAAAATCTGGAGAG	84900
rs577906681	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116795204	TGGGGTCAGGAGTTC[A/G]ACACCAGCCTGGCCA	84900
rs577937939	in-del	-/T	0.00119737	0.0244387	intron-variant	RNFT2	GRCh38.p7	12:116787960	GAGATGGAGTGTCGC[-/T]CTTGTTGCCCAGGCT	84900
rs577962093	snp	C/G	0.00318978	0.0398085	intron-variant	RNFT2	GRCh38.p7	12:116819664	CGCGCGGCCACCAGC[C/G]CCGCCCCGCTGGCCC	84900
rs577965707	snp	C/G	0.00199481	0.0315187	intron-variant	RNFT2	GRCh38.p7	12:116793062	GGTCTGTCAGGAATC[C/G]TCATACCTGGGCCTT	84900
rs577994316	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116786720	AACTTGGTGGCTTGA[A/C]ATAACAGAAATTTGT	84900
rs578030980	snp	C/G	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116760923	TTGCTCTGTTGTCCA[C/G]GCTGCAGTGCAGTGG	84900
rs578032511	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116839580	ATGGACAGATGAGTG[A/G]GTAAATAGGATGGAT	84900
rs578039431	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116792590	ATGATTATTTTATTC[A/G]GTGAGATTAATGTGC	84900
rs578054807	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116746162	GAATCACTTGAGCCC[A/G]GGAGGCAGAGGTTGC	84900
rs578080390	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749528	CAAGTGATCTTCCCA[C/G]CTCTGACTCCCAAAG	84900
rs578141687	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116752751	GGTGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT	84900
rs578161596	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739583	AGAGACGACATTTGC[C/T]CTGCGGGACCAAGCC	84900
rs578175959	snp	C/T	8.5341e-05	0.00653171	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833920	GGGCGGGGTCCTGAT[C/T]GTTCTCTACAGCCTC	84900
rs578228312	in-del	-/C	0.0023933	0.0345097	intron-variant	RNFT2	GRCh38.p7	12:116830532	GGCTCAAGGGATCCT[-/C]CCACCTTAGCCTCCC	84900
rs578236180	snp	A/G	0.0325976	0.123435	intron-variant	RNFT2	GRCh38.p7	12:116775278	AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAAGAG	84900
rs578249812	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774351	TCATCTACCACTGAC[A/G]TCATTTCATAAAAGA	84900
rs578255421	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT2	GRCh38.p7	12:116781289	CAGGGGGCTGACCTG[C/T]GCGAACTATATCAAT	84900
rs578256904	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116747453	GGGAGGATCACTTGA[A/G]CCCAGGAGTTTGAGG	84900
rs745306918	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828740	GGATAAAAGGCAGGA[A/G]GGGAGGGAAGGAAGA	84900
rs745379393	snp	G/T	8.97626e-05	0.00669875	missense, intron-variant	RNFT2	GRCh38.p7	12:116849383	CCGCTCTGCCGCTCG[G/T]TCGCCGTGGACACCC	84900
rs745380559	snp	A/G	3.29777e-05	0.00406051	intron-variant	RNFT2	GRCh38.p7	12:116754075	GGTGAGTCACTTTCC[A/G]ACCTAGTCTCCTGTG	84900
rs745386116	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116812137	ATAAGACCTGACCCT[G/T]ACTTCAAGGGGCTGA	84900
rs745400694	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116759029	TAACATAATCCCAGA[C/T]TTCTTGGAGGCTTTG	84900
rs745428193	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842634	GCTAGAGTGCAGTGG[C/T]ATGGTCTTGGCTCAC	84900
rs745432539	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736567	TTTATCAATGTTCTA[C/T]TCACTTATATATTTT	84900
rs745472634	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116757854	ATTTGTTCCAAGGTA[C/T]AGTTTAAATCCATTG	84900
rs745599888	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810380	AGTGGAAAACAGTTC[A/G]GGGTGTGCGTTTTTC	84900
rs745642693	in-del	-/TCTC			intron-variant	RNFT2	GRCh38.p7	12:116768728	TTTTTTTTTTATTTT[-/TCTC]TCTCTCTCTTTTTTT	84900
rs745659383	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751118	TCGAAGTCTCACTAT[A/G]TTGCCCAGGCTGGTC	84900
rs745682442	snp	A/C			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738076	CCACGTGACCCCGCC[A/C]TACGCCCCGCCTCCG	84900
rs745735140	snp	C/T	8.38293e-05	0.00647361	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766853	TTGTGGATCCTGGCC[C/T]TTCTGGCGGGGAACA	84900
rs745764169	snp	A/G	1.75925e-05	0.00296579	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737834	CGAGCGACAGCCCGA[A/G]GACCAGGGCGAGCAC	84900
rs745772595	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116749656	TTAACTTCATTGCCT[C/G/T]GTATAGACCCTATCT	84900
rs745792964	in-del	-/ACTTA			intron-variant	RNFT2	GRCh38.p7	12:116747064	ATTATTTATTCATTT[-/ACTTA]TTTATTGAGAAAGCA	84900
rs745807216	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800672	TGCAAAAAATTAGCT[A/G]GCACTGTGGTGCGTG	84900
rs745821209	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804341	TGATTCAGAAACTGT[A/G]AGGTGGGGCCAGCAG	84900
rs745827284	snp	A/G	2.23476e-05	0.00334265	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737937	GGCGGCCGGGGCGCG[A/G]AACGCGGCAGGCCCG	84900
rs745845873	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116769810	CCAAGGTGGGTGGAT[-/C]CATTTGAGGTCAGGA	84900
rs745869246	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116762947	GTTAGCCAGGTGTGG[C/G]GGCATGTGCCTGTCA	84900
rs745882354	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844672	AAATATAAAGGGGTC[C/T]TAGCACCAGAATATC	84900
rs745883089	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116813352	TGAATGCCTCTTAGG[G/T]CTGAATCATGCTCTT	84900
rs745902837	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771956	TCTCGAACGGTCAAC[A/G]GTTTCCCTCCTGAGT	84900
rs745912803	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845051	AGTTTGAGACCAGCC[C/T]GGGCAACAAAGTGAG	84900
rs745914213	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784306	TCCGCCGCACGTGTC[A/G]TGTCCTCTTACAATT	84900
rs745918547	snp	A/C/G	7.418e-05	0.00608978	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750211	GGGACGCCCGCCCCC[A/C/G]CCCTGTCCGAGCTGA	84900
rs745935581	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116806391	AAAAAATATATATAT[-/AG]ATATATATAGATAGA	84900
rs745943556	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116741382	GCTATCACAAAAATA[C/T]CATAGAATGGGTGGT	84900
rs746035712	snp	A/T	2.019e-05	0.0031772	intron-variant	RNFT2	GRCh38.p7	12:116833990	AGGAGGGCCCCATTC[A/T]CTAGTCAGGCCTCAG	84900
rs746038319	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797148	CTGGGTCAGCTCCCC[A/G]AATGTTATGGATTGA	84900
rs746042483	snp	A/G	3.29919e-05	0.00406138	intron-variant	RNFT2	GRCh38.p7	12:116754088	CCGACCTAGTCTCCT[A/G]TGGCTGCTGCAACAA	84900
rs746055487	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116838292	ATCGTGTTGATTAAA[C/G]GTTAATTCAAGGGAA	84900
rs746091249	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116796464	ATCCCTGGACAAGAG[C/G]TTCCAGTAGGGTGAG	84900
rs746100604	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835973	AGTCCTTCGACATCT[A/G]TGGACGTGTGGGCGG	84900
rs746113959	snp	A/G/T	8.01772e-05	0.00633114	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750162	GGGTGGGGACCACCG[A/G/T]GGGCACTCGGAGGAG	84900
rs746132479	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830845	AGAGGCAGAGGTTGC[A/G]GCGAGCTGAGATTGT	84900
rs746183888	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116828914	ACTCAGGAAGCCAAG[A/C]TGGCAGGAGGATCAC	84900
rs746199648	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116837049	TAGAAGTTGCTAGAA[C/T]TATCATTGTCATCTG	84900
rs746211212	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116765820	CTACACTGTGGCATT[C/G]CATGGAATGGTCAGT	84900
rs746220662	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795580	TTTCAAGGGCTCAAA[C/T]GCAGAAATGGCTCAC	84900
rs746234865	in-del	-/AGGA	0.00141283	0.0265409	intron-variant	RNFT2	GRCh38.p7	12:116851776	AGAAGGGAGGGAGGG[-/AGGA]AGGAAGGAAGGAAGG	84900
rs746262030	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116806004	CTAGCTAGCTGAATC[A/G]AGACATTAAACTAAA	84900
rs746319335	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116777294	GACATATAAAATATA[C/T]AGAGCAGGGCCTGCG	84900
rs746322527	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746797	GGGTTCCTCTGAGAC[C/T]ATGGGAAGGAACACA	84900
rs746329790	snp	G/T	3.40211e-05	0.00412425	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849484	CAGAAGGACGCCAAG[G/T]GTCAGCATGCCCGGA	84900
rs746417775	snp	C/T	0.000133824	0.00817888	intron-variant	RNFT2	GRCh38.p7	12:116851870	GTCTTTCTCCTCTTC[C/T]TATTCTGTCATCTCC	84900
rs746434486	snp	C/G	0.00026387	0.0114833	intron-variant	RNFT2	GRCh38.p7	12:116779185	CTGACTCTCTCAATC[C/G]TCCCCCCAGCCTCAT	84900
rs746438462	in-del	-/TGGATGGATGGA			intron-variant	RNFT2	GRCh38.p7	12:116789635	TGGATGGGAGGAGAG[-/TGGATGGATGGA]TGGATGGATGGATGG	84900
rs746443348	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116745599	CTGCAGGCCCAGTTT[G/T]TGCAGCCAGGGAAAC	84900
rs746464540	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116817927	CTCTCATTTCATTGG[C/G]GGAAATCACCATTAA	84900
rs746494387	snp	C/T	5.12116e-05	0.00505996	intron-variant	RNFT2	GRCh38.p7	12:116766942	ATCCAACCCCCACGG[C/T]GGGAGAGTGGGGCAC	84900
rs746498035	snp	G/T	4.35189e-05	0.0046645	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737948	CGCGGAACGCGGCAG[G/T]CCCGGGTCCCGGGCG	84900
rs746538804	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746999	TTTTGGTCCACGACT[C/T]AAGGTTGGTTGAATC	84900
rs746621497	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116828917	CAGGAAGCCAAGCTG[G/T]CAGGAGGATCACTTG	84900
rs746653274	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116844294	GGAATGTAGTGGCAC[A/G]ATCTTAGCTCACTGC	84900
rs746685210	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759111	AAAGACCTTGTCTTC[A/G]AGCTCTGAATTTCTT	84900
rs746690644	snp	C/T	0.000592116	0.0171962	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766860	TCCTGGCCTTTCTGG[C/T]GGGGAACACCCTCTA	84900
rs746690768	snp	C/T	3.41758e-05	0.00413361	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849458	TACTAGGACCGAACA[C/T]TGAGGACACCCAGAA	84900
rs746693104	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116800667	AAAAATGCAAAAAAT[A/T]AGCTGGCACTGTGGT	84900
rs746719456	in-del	-/T	2.05446e-05	0.00320498	frameshift-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750245	CTGTGATCTGCTGGC[-/T]CCAGAAAGGACTCCC	84900
rs746768877	snp	A/C/T			intron-variant	RNFT2	GRCh38.p7	12:116812051	GCTCCAGGAGGAGCC[A/C/T]GGTGAGGAACAAATG	84900
rs746773463	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116770431	ACAAGGACCAGGTCA[C/T]CTAAGGATGTGTTTC	84900
rs746811103	snp	G/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740067	AAAAATTGGGTGGGC[G/T]TGGTGTCGCATGCCT	84900
rs746812519	in-del	-/AAA			intron-variant	RNFT2	GRCh38.p7	12:116743083	GAGACCCTATCTCAA[-/AAA]AAAAAAAAAAAAAAA	84900
rs746818653	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835979	TCGACATCTGTGGAC[A/G]TGTGGGCGGAGTTAG	84900
rs746820102	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116822575	AGCACATAGTTAACA[C/G]CTAAGTCACCATCAT	84900
rs746835235	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116819696	GCCTCCTACCTGCTG[C/T]GCTTCTTTCCATCCT	84900
rs746863675	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811520	AGCTGGGATTACAGG[C/T]GCCCACCACCACACC	84900
rs746935413	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116768095	TTACTTTGCACAGTT[A/T]GGCCTTTTTTTTTTT	84900
rs746972623	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795299	TGTAATCCCAGCTAC[C/T]CCAGAGGCTGAGTCA	84900
rs746991284	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790308	GAATGCCAGCTACAT[A/G]CCCCACTCTGTTCTA	84900
rs747066161	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116773548	GACAGAGCGCTTCTG[C/G]TTGGCTTTTCATGGG	84900
rs747101863	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814397	CGGGGAAGGGAGGGC[A/G]ATGCTCTTTTAGACA	84900
rs747158701	in-del	-/AAA			intron-variant	RNFT2	GRCh38.p7	12:116845246	AAGACCCGGTTTCAA[-/AAA]AAAAAAAAAAATATA	84900
rs747201450	snp	C/G	8.61716e-05	0.00656341	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750230	TGTCCGAGCTGAAGG[C/G]TGTGATCTGCTGGCT	84900
rs747203185	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116749349	GTGGCGAGATCTTGG[C/T]TCACTACAGCCTCAA	84900
rs747258217	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116825455	GATTATCATGAGGGC[C/G]AGTACTAGCTGTATC	84900
rs747271884	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116756341	TTTTGTTTTGCAGCT[A/G]TTGTAAAAGGGGTTG	84900
rs747309447	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839622	CGGATGGATGGAATG[A/G]TGTCCAAGTGGAGGA	84900
rs747332480	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116795820	GTCAACGAAACTGGG[G/T]TCAAATCCTGGCTTC	84900
rs747429302	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116808633	GTTGTTCCGCCACTA[A/G]AGAAGATGAAAAACA	84900
rs747439789	snp	A/G	0.000146338	0.00855263	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750071	GCCGGGGCGAGGGGG[A/G]CGCCTACCACCACCG	84900
rs747455083	snp	C/T	0.00016472	0.00907375	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779270	GGGGATCGCAGACTT[C/T]GTTCTGAAGTACATC	84900
rs747457484	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736344	AGAAGGGACAACACG[C/T]GACTGTGAGGAGGTG	84900
rs747542052	snp	A/G	1.68417e-05	0.00290182	intron-variant	RNFT2	GRCh38.p7	12:116779387	GGTAGCCCCAGTCAC[A/G]TGGATCATGCAGAGG	84900
rs747545250	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116760973	AGCCTCCAACTCCCG[G/T]ATTCAAGCAATCCTC	84900
rs747574044	snp	A/G			downstream-variant-500B	RNFT2	GRCh38.p7	12:116854083	GATAGGAATCTGGCA[A/G]AAGGGATCAGAAAGG	84900
rs747615402	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831496	ATTATAGATCTCTAA[C/T]ATAATCAGACCCTCT	84900
rs747626578	snp	G/T	0.000190967	0.00976971	intron-variant	RNFT2	GRCh38.p7	12:116748694	CCCTCTGGGGAACTG[G/T]GGGCCATTGAACTTG	84900
rs747686159	snp	C/G	7.74743e-05	0.00622344	intron-variant	RNFT2	GRCh38.p7	12:116766960	GAGAGTGGGGCACTT[C/G]GCTGGGCTTGGGGCA	84900
rs747695497	snp	A/C			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736716	AAGCACTCAACCTGG[A/C]CTTCTAGACAAACTT	84900
rs747716773	in-del	-/AGAAC	3.29639e-05	0.00405966	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852719	GGTGTGTAAGGAAAT[-/AGAAC]AGTCTGCTGGGAGTC	84900
rs747735986	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116818933	TAAAGGTGCAGAGGT[G/T]TGGGGTACAGGTAAG	84900
rs747753788	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116748162	ACCACTGCACTCCAG[C/G]CTGGGTGACAGAGCA	84900
rs747754882	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116778736	GGTGCCTGTAATCCA[C/G]CTACTTGGGAAGCTG	84900
rs747759865	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116791216	ATTTTGTGTAAGTGG[A/T]ATAATACCCTATGTG	84900
rs747780143	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818047	CGGGAAAGGGCTTTC[C/T]CTGTGGGATGGACAT	84900
rs747791287	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791902	AAGAAAATGAAAACA[A/G]CCAGAGGCTAAGAAA	84900
rs747792080	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799702	TTTTTTGGTAGAGAC[A/G]GGGTTTCACCATGGG	84900
rs747820434	snp	C/T	1.64819e-05	0.00287066	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116741084	AACACGGATAACATT[C/T]CACCTGAAAGGTAGG	84900
rs747835031	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116830580	GGTGTCAGCCATTGC[A/C]CCTGGCCTATTGACA	84900
rs747846958	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818941	CAGAGGTTTGGGGTA[C/T]AGGTAAGGAGAAGAA	84900
rs747858577	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779240	GCTGGACTTCTTTGA[C/T]CTGCTATGGATTGTG	84900
rs747875432	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845468	TAAAACAGGGGAGAC[A/G]TGATTGCTTGGCTGA	84900
rs747876643	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761171	TTTTTCTTTTTGAGA[C/T]GGAATCTTGCTCTGT	84900
rs747884112	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116801605	ACAAGTCAAGTGCTG[G/T]CTGGTTAGTTAATTA	84900
rs747896982	in-del	-/AGTG			intron-variant	RNFT2	GRCh38.p7	12:116766144	TAATTAGCCAGGTAT[-/AGTG]AGTGACACCTGCCTG	84900
rs747898035	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116817043	TTTGAGATGGAGTCT[C/T]GCTCTGTCGCCCAGG	84900
rs747942440	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760271	CTGCCCCAGACTATC[C/T]GCCTCCCAGCTGCCA	84900
rs747948951	snp	A/G	1.65026e-05	0.00287246	intron-variant	RNFT2	GRCh38.p7	12:116753949	AGGCCTGATGAGTCT[A/G]AGTGGGTGACATCAG	84900
rs747988307	in-del	-/GGAT			intron-variant	RNFT2	GRCh38.p7	12:116788960	TGGGAGGAGAGGGAT[-/GGAT]GGATGGATGGATGGA	84900
rs747993905	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813197	CTCTTGGTCTCAAGC[A/G]ATCCACCCACCTTGG	84900
rs747998870	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844524	ACAGGCGTGAGCTAC[C/T]GTGCCTGGCCATTAT	84900
rs748016624	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116800279	GGGCGGGCAGATCAT[C/T]TGAGGTCAGGAGTTC	84900
rs748036421	snp	A/G	6.59044e-05	0.00574002	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835987	TGTGGACGTGTGGGC[A/G]GAGTTAGGAAAGCCC	84900
rs748056141	snp	G/T	2.60563e-05	0.00360936	intron-variant	RNFT2	GRCh38.p7	12:116741106	AAAGGTAGGCATCCC[G/T]GCTTCTGTTCCATCT	84900
rs748096887	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116764278	CAGGTGATGGGTGCA[C/T]GAAAATCTCACAAAT	84900
rs748142706	snp	A/G	0.000230858	0.0107413	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836194	AGAACTATGGAGTCC[A/G]AGCCACCGGGCAGCA	84900
rs748175778	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116835238	TCACTCAGGTAAAGA[C/T]AACAGAATAAGCATT	84900
rs748176929	snp	A/G	1.66821e-05	0.00288804	intron-variant	RNFT2	GRCh38.p7	12:116833760	TGGGTCTTTACTGCT[A/G]ATAATAATTGATGTT	84900
rs748270090	in-del	-/TG			intron-variant	RNFT2	GRCh38.p7	12:116822361	GTCTCTCTCTCTCTC[-/TG]TGGCAATTCCAGCTG	84900
rs748296437	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116834080	AGGGAAAATTCATAC[G/T]ACATGAAATTAACCA	84900
rs748335956	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116769989	ACAGTAAGCCAAAAT[C/T]GTGCCACTGCATCCA	84900
rs748393808	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791345	AGACGGAGTCTCACC[A/G]TGTTGCCCAGGCTTT	84900
rs748419536	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773945	TGCGGTATGTACATA[C/T]AGTGGAATATTATTC	84900
rs748450018	in-del	-/TTT			intron-variant	RNFT2	GRCh38.p7	12:116750909	ATATATATATATATA[-/TTT]TTTTTTGAGACAGGG	84900
rs748456401	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116826384	CCGTTTCCCCTTCAC[A/G]GTGGCAGGGAGGCGA	84900
rs748468190	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116744117	TGTAGTCCCAGCTAC[C/T]CAGGAGGCTGAGGAA	84900
rs748512415	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784486	TGTCAGCTGGTACGA[A/G]AAAACATGGCTGCCT	84900
rs748558319	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116757558	AGAATTTTTTAATTT[C/G]CATCTTGATGTCATT	84900
rs748615558	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116841189	AGGCATGGTAGCTCA[C/T]GCCTATAATCCCAAC	84900
rs748628665	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780363	GCATTGGATTCTCAT[A/G]GGGAGCATACAACCT	84900
rs748639507	in-del	-/AAAAA			intron-variant	RNFT2	GRCh38.p7	12:116743081	GTGAGACCCTATCTC[-/AAAAA]AAAAAAAAAAAAAAA	84900
rs748696972	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797429	GCCAGGTTTGGTGGC[A/G]TGTGCCTGTAATCCC	84900
rs748709554	snp	C/T	0.000145085	0.00851596	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750074	GGGGCGAGGGGGGCG[C/T]CTACCACCACCGCCA	84900
rs748817449	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116840198	AAGGCAAGAGGGCAA[A/G]AGAATGGTGACTCCT	84900
rs748833053	snp	A/C/G	1.77889e-05	0.00298231	intron-variant	RNFT2	GRCh38.p7	12:116749799	AGTAAGGTCTTTTCC[A/C/G]TCTGCCTGACTTCCT	84900
rs748867150	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116810289	TGAGTTTTAAAGCAG[C/G]GCTGGGAGTTACCCA	84900
rs748892916	snp	C/T	3.33433e-05	0.00408296	intron-variant	RNFT2	GRCh38.p7	12:116779363	GGTAGGCACTGGCTG[C/T]GGCCACAAGGTAGCC	84900
rs748900193	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768434	TACAGTCATGTGTCA[C/T]GTAATGATGTTTCTG	84900
rs748913106	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116809148	CCCTCCCCCAGGAAC[A/T]GAAGAACACAGAGGC	84900
rs748922655	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816812	CTTAAAAAAATAACA[C/T]GTATGAGGTATAAAA	84900
rs748939307	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116804784	CCAGCCTAGGCAACA[C/T]GACAAAACCTTGTCT	84900
rs749003724	snp	A/G	6.8299e-05	0.00584336	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749928	GGCAGCCTCCCCACC[A/G]GCGCTCTTCTCGGGC	84900
rs749014850	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116833634	TCTCCCTGGCCATAT[C/T]GCAGCCCCATTAGGA	84900
rs749015799	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736855	CTACCAATCAAGTTA[C/T]GCACAAAAAGCATAA	84900
rs749035535	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116792074	TTTTTTGTTTTTTGA[A/G]ACAGAGTCTCTGTTG	84900
rs749136175	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831793	GTTTTGGCAAACGTG[C/T]GCACCCATGTATCCC	84900
rs749151459	snp	C/G	3.15901e-05	0.00397417	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737918	CGGCGCGGACGTGGG[C/G]CGCGGCGGCCGGGGC	84900
rs749160124	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116791475	CGCCACCAGGCCTGG[A/C]TAATGTTTGTATTTT	84900
rs749228829	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782582	AATTTTCTAAAAGAC[A/G]TGGACATTTTTGGGT	84900
rs749233789	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116760422	ATTTGCTTCTCCCTG[A/T]GGAGTTTTAGCCCTT	84900
rs749258920	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116749071	TTTGTATTAGTTCCT[A/G]GGACTGCCGTAACAA	84900
rs749265577	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814232	TATTTTTTGGCCACC[C/T]ATTCTGTACCAGGCC	84900
rs749305045	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772743	TTGTTGTGGAAGTTG[C/T]AGTGTGCAGAACATG	84900
rs749312378	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822773	TTGGGAGGCTGAGGC[A/G]GGCAGATCACCTGAG	84900
rs749319745	snp	G/T	1.72377e-05	0.00293573	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750090	CTACCACCACCGCCA[G/T]CCCCACCACCATTTC	84900
rs749328913	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116850457	ATTACAGGTATGAGC[C/G]CCTGTGCCCAGCCCA	84900
rs749341757	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116752605	AAGTGCGACCAGGTA[C/T]GGTGGCTCACGCCTG	84900
rs749362874	snp	C/T	3.29544e-05	0.00405908	intron-variant	RNFT2	GRCh38.p7	12:116833973	GCTGGAGGGCCGGCC[C/T]AAGGAGGGCCCCATT	84900
rs749368652	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116796332	TAGCTGAACTGATTT[C/T]TCTGAATAACACAGC	84900
rs749419925	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116795352	GGCAGAGGTTGCAGT[A/G]AGCCGAGGTCACACC	84900
rs749501248	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116835401	TGCTTTTCTTTTCAT[C/T]ATTAGTACAAATCAG	84900
rs749546368	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116805882	CAGGATATCAAGGAA[A/G]ATCTTCATTGCTTAT	84900
rs749558734	snp	C/T	1.6766e-05	0.00289529	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833902	CTCCAACAGCTACTT[C/T]CTGGGCGGGGTCCTG	84900
rs749559021	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116787521	GACTAGCCTGGGCAA[C/T]ACAGCAAGATGCCAT	84900
rs749568089	in-del	-/TC			intron-variant	RNFT2	GRCh38.p7	12:116849799	TTCTTTTCTTTTCTT[-/TC]TCTCTCTCTCTGTTT	84900
rs749613995	snp	A/G	3.3757e-05	0.00410821	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849470	ACACTGAGGACACCC[A/G]GAAGGACGCCAAGGG	84900
rs749623776	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831271	TTTCTCATGATTAGA[C/T]TAGAATTTATTGCTG	84900
rs749656890	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116753873	ATTTTTCTCTCTCTT[-/C]TGTCAACTCTGAGGG	84900
rs749680372	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815786	TTATTCAGCCTTCCA[C/T]ATCCCCTACTTTGCT	84900
rs749715119	in-del	-/A	6.41457e-05	0.00566293	frameshift-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749910	TGAGAGTCTGAAGGC[-/A]GAGGCAGCCTCCCCA	84900
rs749725036	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116755088	TAGAAGGGTTTTTCC[A/G]ATGTTATCTTCTAGA	84900
rs749728040	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116828383	GGTTCATGGCTCACA[C/G]TTTGGGTGGCTGGAA	84900
rs749767692	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786825	ACTGCCTCCGGAGGC[C/T]CAAGGAGAGAATCTG	84900
rs749768243	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116799150	GTAGGACTTGAGGTC[C/G]TCCATCCTTGCTGGC	84900
rs749782479	in-del	-/CT			intron-variant	RNFT2	GRCh38.p7	12:116799305	CCAAGCCCAAGAAAA[-/CT]CTGCTTTTAAAGGGC	84900
rs749835130	in-del	-/CAGAAGTCAC			intron-variant	RNFT2	GRCh38.p7	12:116775329	CCTTACTGAAGTCAC[-/CAGAAGTCAC]CAGTCTAGACGGTGC	84900
rs749838206	snp	C/G	7.19243e-05	0.00599641	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849397	GGTCGCCGTGGACAC[C/G]CTGCGCTGCTGGAAG	84900
rs749884543	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116844117	TGGCCTTTTCACTCT[G/T]GTTCTTTCATGAGTA	84900
rs749929112	snp	A/G	3.4525e-05	0.00415467	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750175	CGGGGGCACTCGGAG[A/G]AGGGAGGCGACGAGC	84900
rs749932388	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116812923	TTCAGAGGCAAGGGA[A/G]TCCTTTGGTTTTCTG	84900
rs749933262	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783504	GCTGCAGCCATCAGC[C/T]GCCTCGTCAAGGTGG	84900
rs749987672	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811895	CTTACTAGTTACCAA[C/T]AGGCACCAGCCCTGG	84900
rs750064745	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739928	GTTTCAAAGAGGGCC[A/G]GGCATGGTGGCTTAT	84900
rs750068386	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116806618	TTAGCTGAGCACGGC[A/G]GTGCACACCTGTAGT	84900
rs750099505	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751508	TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	84900
rs750107156	snp	A/G	6.29901e-05	0.00561169	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750122	ACCATGGCGGCCACC[A/G]CGGGGGCTCCCTGCT	84900
rs750125843	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116822480	AGGTTATCTAACTTT[A/T]CTGTGCCTCCATTTC	84900
rs750154738	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116752167	CCAGCCTGGGAAACA[C/T]AGTGAGACCCTATCT	84900
rs750156381	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116796046	CCCAAGTAGCTGATA[C/T]TACAGGCGCCCACCA	84900
rs750172779	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116827048	AACATGGTGAAACCC[G/T]GTCTCTACTAAAATA	84900
rs750175095	snp	C/T			synonymous-codon, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836234	AGCTGGTGACATCTG[C/T]GCCATCTGTCAGGCC	84900
rs750193491	in-del	-/TTCCTTCCTTTTTTT/TTCCTTTTTTTTT			intron-variant	RNFT2	GRCh38.p7	12:116849845	TCCTTCCTTCCTTCC[lengthTooLong]TTTTTTTTTTTTTTT	84900
rs750198101	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116831196	TGACCTCGTCTCTCT[-/A]ACAAAAAAAAAAAAG	84900
rs750210083	snp	A/G	0.000202819	0.0100682	intron-variant	RNFT2	GRCh38.p7	12:116741003	CAGTGGGAGTGTTGG[A/G]AGACTCTGGCTCACC	84900
rs750211620	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795127	TATGAAAATGAAGGC[C/T]GGGCCCGGTGGCTCA	84900
rs750255395	snp	C/T	3.54755e-05	0.00421147	intron-variant	RNFT2	GRCh38.p7	12:116741144	CTAGGCTTCGGGTGG[C/T]GAGGGGCAACCCAAA	84900
rs750298657	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116764209	ACTCTGGGGGAAAGA[A/G]TGGGAAGGGAGTGAG	84900
rs750304995	snp	A/G	8.66288e-05	0.0065808	missense, intron-variant	RNFT2	GRCh38.p7	12:116849428	GACGGCGCCACGTCC[A/G]CACACTTCCAGGTGT	84900
rs750328272	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817328	TGTTTTTATTTTTTA[A/G]ATAGAGACAGGAGGT	84900
rs750364762	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848079	TCAGCTCTGATTTAT[A/G]AGTGAGAACATGTGG	84900
rs750378736	snp	A/G	0.00014299	0.00845426	intron-variant	RNFT2	GRCh38.p7	12:116851766	AAAAGAAAGAAAGAA[A/G]GGAGGGAGGGAGGAA	84900
rs750390917	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116795168	CCCAGCACTTTGGGA[A/G]GCCAAGACAGGTGGA	84900
rs750394255	in-del	-/AGA			intron-variant	RNFT2	GRCh38.p7	12:116774824	GAGGTGGAGTTTCCC[-/AGA]ACCTTGGATGAATTT	84900
rs750405591	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738003	CCCCATCCCTCCAGG[C/T]AGGCGCCGGCCCCGC	84900
rs750409986	snp	C/T	0.000203397	0.0100825	intron-variant	RNFT2	GRCh38.p7	12:116766939	GGAATCCAACCCCCA[C/T]GGTGGGAGAGTGGGG	84900
rs750412882	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116840594	TCAGAGTTCTTGACA[C/T]CTACCTCTGACTCCT	84900
rs750421485	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774661	TAAGGACTGAGTGGT[C/T]TTGCCATCTTCTGAG	84900
rs750430048	snp	C/T	0.00057241	0.0169079	intron-variant	RNFT2	GRCh38.p7	12:116851992	GATGTTTCCACCAAC[C/T]AGGGTAGTGGCATGG	84900
rs750439968	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116836822	CTAGTCCCAGCTACT[C/G]TGGAAGCTGAGGCAG	84900
rs750442598	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116744953	GTACCTGCCAGGGCT[C/G]TTGCTTTCTGAGCTG	84900
rs750457161	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116825188	TCCTCCAATTAGTCT[C/T]AGAGCTGCTCCCCTT	84900
rs750538512	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116756173	TAGGGTCATTTTCAC[A/C]GTATTGATTCTACCC	84900
rs750556917	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768884	TACAGGTGCTCACCA[C/T]TACGCCCGGCTAATT	84900
rs750580973	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839223	CTCCTGGTGAATCAC[A/G]AGCAACATGAGAGCA	84900
rs750581074	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116757577	CTTGATGTCATTTTT[C/G]ATCCAATGCTCATTC	84900
rs750608919	snp	C/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737249	ATGCGCACCTCTCCC[C/G]ACCCTCGGACGCCCC	84900
rs750611880	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116767859	CTGGGATTACAGGCG[A/T]GAGCCACTGCCCCTG	84900
rs750618645	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116808503	AGCAGGGACAGGGCC[A/C]CAGCAGGCACCTGGG	84900
rs750621237	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853400	GAGGGAATAAGAAAG[A/G]CAAGCTTTGGACACA	84900
rs750627259	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116833330	CTTATTGCCTGGCCT[C/T]ACCTGCATTCTGTGC	84900
rs750674190	snp	C/T	0.000136603	0.00826333	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749870	CGCTCAGCTCCGAGG[C/T]GAGTGTGGATGAAGG	84900
rs750701949	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116800625	GGTGACAGAGCAAGA[C/T]TCTGTCTCAAAAAAA	84900
rs750739050	snp	C/G	2.06956e-05	0.00321673	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737773	GGAAGGGGAGGAGGG[C/G]AAGGGCGGCCACTGA	84900
rs750804070	snp	A/C	1.64784e-05	0.00287035	utr-variant-3-prime, missense	RNFT2	GRCh38.p7	12:116852702	AGATTGATGAAAGTG[A/C]AGGTGTGTAAGGAAA	84900
rs750806345	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818695	TGGGGAAGGTGGTGT[C/T]GAGTAATTGAAAGGC	84900
rs750857776	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116743247	AAAAAAAAAAAAACC[-/G]GTTAAAAAACACTCA	84900
rs750859327	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831306	TTGGTGAGAATACCA[C/T]AGAAGTGATACTGTG	84900
rs750888806	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760944	AGTGCAGTGGCATGA[C/T]CATAGCTCATTGTAG	84900
rs750889029	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116767303	GCTCACTGCAGCCTC[A/G]ACCTCCCAGGGCTCA	84900
rs750901306	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116790492	AACTTGCAAAAGAGC[A/G]CAAACCTTGCAGTAA	84900
rs750962680	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116845041	TGAAGCCAGGAGTTT[C/G]AGACCAGCCTGGGCA	84900
rs750963535	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759926	AACTCTCGAGTTTCT[A/G]TGGCCTTTGTCTTCC	84900
rs750979582	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831593	CTATAGGCACATCTT[C/T]GCACCTATCTCTGAT	84900
rs750992647	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116846111	ACCCACTGTACACCA[G/T]GCTAGGAATGAAGGG	84900
rs751008964	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116772416	GGTTCAAGCGATTCT[C/G]CTGCCTCAGCCTCCT	84900
rs751014627	in-del	-/AGG			intron-variant	RNFT2	GRCh38.p7	12:116781985	TCGGGAGGCTGACGC[-/AGG]AGAATTGCTTAAACC	84900
rs751025661	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116846205	ATAATCATTATTACT[A/G]TCATAATAGCTAATA	84900
rs751065011	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116802647	GACTTTCTTCTCTAG[A/G]GTCTCCAGAGGGAAT	84900
rs751079932	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814009	AAGTGCTAGGCTCGA[C/T]TTATCAATTAGTGAA	84900
rs751089159	in-del	-/CAAA			intron-variant	RNFT2	GRCh38.p7	12:116775261	GTGAAACTCCCGTCT[-/CAAA]AAAAAAAAAAAAAAA	84900
rs751114822	in-del	-/GATGGATGGATG			intron-variant	RNFT2	GRCh38.p7	12:116788830	ATGGATGGATAGATG[-/GATGGATGGATG]GATGGATGGATGGAT	84900
rs751138070	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761102	CACGTACACCTAGCC[C/T]AGTCCCTTTACGCCG	84900
rs751163111	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801434	AATCGTCGAAAGAGC[A/G]CATACTATACCCTAA	84900
rs751183308	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116742124	ACCAGCAATAGTCAG[A/G]GGGCAGAAAGGACCG	84900
rs751191088	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116772592	TTACAGGTGTGAGCC[A/G]TTGCGCCCAGCCCAA	84900
rs751199532	in-del	-/CTTA			intron-variant	RNFT2	GRCh38.p7	12:116848457	CCCTACCATGGGCCC[-/CTTA]CTTCTCTCAGAATAA	84900
rs751200581	snp	C/T			intron-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116824997	GGTCAGGAGTTCAGT[C/T]AGGACACACCGGGTA	84900
rs751202230	in-del	-/AATATAT			intron-variant	RNFT2	GRCh38.p7	12:116771492	AAAAAAAAAAAAAAA[-/AATATAT]AAATACGTATATGAG	84900
rs751207207	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748325	CGGGCTCTCTGCTCC[A/G]CCAGCAGTGGCTCTG	84900
rs751228775	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771258	TGAGCCCAGGAGTTC[A/G]AGACCATCCTGGGCA	84900
rs751277788	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823561	CCGTGGCGCATACCT[A/G]TAATCCCAGCTACTC	84900
rs751288125	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116783915	CCGTGTACTGGCCAC[A/T]GTCCCAAGTACTTTA	84900
rs751330335	snp	A/G	6.34417e-05	0.00563177	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749883	GGCGAGTGTGGATGA[A/G]GGTGGCGTCTTTGAG	84900
rs751339257	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796905	AGGGGCTGGAAGAAG[A/G]TTAAGTAGTGATTCC	84900
rs751372760	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116782764	CTCACATGCCGAAAA[A/T]AAGTCTGAACACACA	84900
rs751411502	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116850286	CAGCCTCCCAAGTAG[C/T]TGGGACTACAGGTGT	84900
rs751425130	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794976	ATGAAACTTGGTTTT[A/G]TATTAACTTAGCCCA	84900
rs751436800	snp	A/G	1.64735e-05	0.00286993	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779230	ACCTGGAGATGCTGG[A/G]CTTCTTTGACCTGCT	84900
rs751447184	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808078	AAGTCGTTCTCCTGC[C/T]TCAGCCTCCCAAATA	84900
rs751449800	snp	C/G	1.64762e-05	0.00287016	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852642	CGGAAAGATCATCCT[C/G]CCTGCAGATGCTGTT	84900
rs751479528	in-del	-/TT			intron-variant	RNFT2	GRCh38.p7	12:116778131	CTTTCTTTTCTTCCC[-/TT]TCCTTTCTTCCTTCC	84900
rs751519586	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778145	CCTCCTTTCTTCCTT[C/T]CTTCCTTTTGCCTCC	84900
rs751526665	snp	C/T	0.000191186	0.00977531	intron-variant	RNFT2	GRCh38.p7	12:116748652	CTCTCTGCCGCCCAC[C/T]CAATGTCAGCTGTGA	84900
rs751526711	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779315	GTGCCTCATCGTGGC[C/T]CTGCCCAAGATCATC	84900
rs751619710	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116830150	TCATTCCTCTTCCCC[-/T]AATGTTGATATCTGA	84900
rs751624015	snp	A/G	3.29544e-05	0.00405908	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754019	ATGGCCAGCACCTTC[A/G]CCTATGCCAACTCCA	84900
rs751629786	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786557	TGAGGTTACTCATCA[C/T]CTGGCGCCTTCTGGG	84900
rs751646672	snp	C/T	6.77163e-05	0.00581838	intron-variant	RNFT2	GRCh38.p7	12:116766771	TCTGGAAGGTTCTGC[C/T]ACATGCACCTTTGAT	84900
rs751648419	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815492	CTAGAAGCTCCCTGC[C/T]CTCCTTGCCTCTGGT	84900
rs751677676	snp	A/G	3.76301e-05	0.00433747	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836185	CTCCCTCAAAGAACT[A/G]TGGAGTCCGAGCCAC	84900
rs751682562	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116842115	CATCCAAGCTCCGCC[A/G]TGTGGTTGCTGGTAG	84900
rs751682699	snp	A/C/G			intron-variant	RNFT2	GRCh38.p7	12:116826351	TCCATGCCCAAGCAC[A/C/G]TCCTGCAACAATTGC	84900
rs751721821	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116776449	GAGCAGAGCTAAAGA[C/T]GGGAGCTCAGGGCCG	84900
rs751742998	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798077	CTACCTCACTAGGAC[A/G]GGCCCTGGTCCAATA	84900
rs751748497	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116769838	GGAGTTTGAGACCAG[C/T]CTGACCAACATGGTG	84900
rs751756736	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798814	CTCCTAAGCTCAAGC[A/G]ATCTACCTGCCTCCG	84900
rs751803131	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116841023	TTTCCCAGATTCCCT[A/G]TAATGAGTAAGGGTT	84900
rs751804486	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799015	ATTGAGTTTTCTACA[A/G]AGGGTCTCACAAGGC	84900
rs751810566	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738412	CTTTTCTCCCATCAT[A/G]GTCTGTGTAGTCTCC	84900
rs751835373	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116810732	AGCCAGGCTCCCTGA[C/G]GGGGCCTTGGAGGTG	84900
rs751842654	snp	C/G	5.6823e-05	0.00532994	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836265	GAGTTCCGAGAGCCT[C/G]TGATTCTCCTGTGCC	84900
rs751851433	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116780410	GTGCAGTTCACAATA[C/T]GGTTCCCACTCCTAG	84900
rs751857298	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116818038	TTAGGGAAACGGGAA[A/G]GGGCTTTCTCTGTGG	84900
rs751934573	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768222	TCTCCTGTCTCAGCC[C/T]CTTGAGTAGCTGGGA	84900
rs751943376	snp	C/T	3.31268e-05	0.00406968	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833869	GCTGTGGTACAAATA[C/T]ATCATGGGTGACGAC	84900
rs751969718	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820962	CTTGCTGGGTCTCCC[A/G]CTCTGTTCTTCCCTC	84900
rs751983646	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737376	GAGGATGTCAGGGAA[A/G]AAAGGGAGTAAAGGA	84900
rs751987267	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116765364	CCTGGAATAATGGGT[A/G]GATGGAGATGCATTT	84900
rs751992488	in-del	-/TA			intron-variant	RNFT2	GRCh38.p7	12:116741519	TGGCCATTCTTTTGC[-/TA]TGTCTTAATGTGGTG	84900
rs751995696	snp	C/G			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738208	TCGCGTGAGTGCTGC[C/G]GGCGTAGCTGTGCCC	84900
rs752019905	snp	A/C			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853505	ACTCGGGATTAGAAG[A/C]AAGAGAGGTAAATAA	84900
rs752033014	snp	A/G/T	0.000108884	0.00737776	intron-variant	RNFT2	GRCh38.p7	12:116833950	CTGCAAGGTGAGGTG[A/G/T]CCCCAAGGCTGGAGG	84900
rs752070657	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116748046	AATACAAAAATTAGC[C/T]GCACATGATGGCAGG	84900
rs752083385	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116749096	TAACAAAGTACCACA[A/C]CCCAGGGGGCTTAAA	84900
rs752088757	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820236	GCTGGGTCTACAGGC[A/G]TGCGCCATCATGCCT	84900
rs752115358	snp	A/C/G	1.65067e-05	0.00287282	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779337	AAGATCATCCTGGCT[A/C/G]TCAAGTCCAAGGTAG	84900
rs752119590	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116793429	CTGGGCTCAAGTGCT[C/T]CTCCCACCTCAGCCT	84900
rs752133746	in-del	-/TATATATAT			intron-variant	RNFT2	GRCh38.p7	12:116750842	ATAATATATATATTA[-/TATATATAT]AATATATATTATATA	84900
rs752136998	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823318	AAGTCACACAGATAC[A/G]GAGGATGCGCACCTA	84900
rs752138662	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116800650	AAAAAAAAAAATGGT[A/T]TAAAAATGCAAAAAA	84900
rs752141069	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116834722	TTGAGGTTCATCCAC[A/G]TTGTAACATGTATCA	84900
rs752142368	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833233	CCCTGTTCTTTCTCA[A/G]CACAACTAGGTATTC	84900
rs752158146	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116792065	AAATTTTCTTTTTTG[-/T]TTTTTTGAGACAGAG	84900
rs752246152	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116803873	ATGAAAGGTTTTTGG[A/C]CCAAGGCAGTGGTGC	84900
rs752267740	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116833361	CCATCCTGCCCAGGC[A/C]CCTGAGAGCAGTCGC	84900
rs752286333	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116763936	AATTCACAATTTCAA[A/T]AATGTAGAACCATCC	84900
rs752308240	snp	C/T	1.65097e-05	0.00287308	stop-gained, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833834	CTGAGCCAGCTGTTC[C/T]GATCCCTTGTCCCCA	84900
rs752309601	snp	G/T	2.10577e-05	0.00324475	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737770	AAGGGAAGGGGAGGA[G/T]GGGAAGGGCGGCCAC	84900
rs752336938	in-del	-/AAAA			intron-variant	RNFT2	GRCh38.p7	12:116775262	TGAAACTCCCGTCTC[-/AAAA]AAAAAAAAAAAAAAG	84900
rs752339579	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116762244	AATTAGCCAGCCATG[A/G]TGGCTCACACCTGTA	84900
rs752413880	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116772655	AACCCATTTAAAAAG[G/T]ACCAAAAACACCTCC	84900
rs752428837	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791946	ACATAGCTCACAAGT[A/G]GCTATGTGGAGATTT	84900
rs752435359	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116743679	ATACATCCAAGGGGC[A/G]GGCAGCCAAGCCTTC	84900
rs752459496	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773241	TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC	84900
rs752512370	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116784681	AATAACCTGGAAAGG[A/T]CCTCTAACTCTTCCT	84900
rs752521038	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116742171	CACAGCCTTTATTGT[A/G]TTTTCTGGGGGAAAG	84900
rs752523858	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814151	GCCAGTCACCATGCA[C/T]GTACTACCTGCCAGC	84900
rs752533728	snp	A/G	6.60437e-05	0.00574608	intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836285	TCTCCTGTGCCAGGT[A/G]AGCAGGGCTCAGGCG	84900
rs752556856	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116756046	TGCTTCAGTTATGTG[A/G]GCTCTTTTCTGGTTC	84900
rs752595603	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839040	TGAATGAATGACTTG[A/G]TTGCGATGTTGCTTC	84900
rs752633551	snp	C/T	3.56182e-05	0.00421994	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750033	GTTCATCCAGATGCC[C/T]GCGTCCAGGGAGGAA	84900
rs752640392	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116806385	AAAAAAAAAAAATAT[-/AG]ATATATATATATATA	84900
rs752648000	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797001	TGGTATTTAGTGGAC[A/G]GAGACCAGGGGTGCT	84900
rs752749373	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116753895	CTCTGAGGGGACCAG[A/G]GATGTGCCTTTTCCC	84900
rs752760350	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116817500	TATTAAAGGTGAGAG[C/G]ATAAGCTGTATAACC	84900
rs752783684	snp	A/G	6.27805e-05	0.00560235	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740520	TCTTCACAGTGAATC[A/G]GGTGACACGTCTCCA	84900
rs752796355	snp	C/T	2.23811e-05	0.00334516	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737901	CGCCAGGTTCACCAT[C/T]CCGGCGCGGACGTGG	84900
rs752799821	snp	A/C	8.82379e-05	0.00664162	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766880	AACACCCTCTATGTG[A/C]TTTATACATTCAGCT	84900
rs752813445	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116816640	TCAAATCCCACCTCT[C/G]CTACATCTGAGCTCT	84900
rs752826066	in-del	-/CGCCACACCATGGC	1.8528e-05	0.00304362	upstream-variant-2KB, frameshift-variant	RNFT2, C12orf49	GRCh38.p7	12:116737872	TTCCGCAGAAGCCGG[-/CGCCACACCATGGC]CGCCAGGTTCACCAT	84900
rs752867808	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116762778	CACCATGCCTGGCTA[A/G]TTTTTATATTTTTAG	84900
rs752914188	in-del	-/AAA	0.000428082	0.0146239	intron-variant	RNFT2	GRCh38.p7	12:116851744	AGTGAGACTCTGTCT[-/AAA]AAAAAAAAGAAAGAA	84900
rs752936284	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116828251	GCTTCTCAAACTTGG[A/C]TGTGCACTCGGGTCA	84900
rs752941929	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116759671	TCTACCTGGCTCCAG[C/G]CTGGTACTGGGGGTT	84900
rs752969727	snp	C/T	5.44647e-05	0.00521818	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750132	CCACCGCGGGGGCTC[C/T]CTGCTGCAGCACGTG	84900
rs752982462	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116843348	AAATACAAAAATTAG[C/T]TGGGTGCCATGGTGC	84900
rs752985409	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799728	ATGGGAGGCTGATGT[A/G]GGCAGATCACCTGAG	84900
rs752998069	snp	A/G	6.73106e-05	0.00580093	intron-variant	RNFT2	GRCh38.p7	12:116766776	AAGGTTCTGCCACAT[A/G]CACCTTTGATATCAC	84900
rs753016301	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842869	GTGAGCCACTGTGCC[C/T]GGCGTGTTTATACTT	84900
rs753072383	snp	A/C	1.64857e-05	0.00287099	intron-variant	RNFT2	GRCh38.p7	12:116835944	CATTTCAGCCACCAC[A/C]CTGCTCTCCTTTCAG	84900
rs753083357	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116769917	GCAGGATCCTGTAAT[C/G]CCAGCTACTTGGGAG	84900
rs753163992	snp	C/T	5.56127e-05	0.00527288	intron-variant	RNFT2	GRCh38.p7	12:116833960	AGGTGGCCCCAAGGC[C/T]GGAGGGCCGGCCTAA	84900
rs753217565	snp	A/C			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738710	GATGCATCCCGCGTG[A/C]AAAAATTTATTCCAG	84900
rs753262932	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780461	GATCTGATGGGAGGC[A/G]GAGCTCAGGCGGTAA	84900
rs753316198	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116750563	GGATAGAAACTTCCT[C/T]GCTGGTTGGCTGGTG	84900
rs753351800	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116767390	CACCTGGCTAATTTT[C/T]ACATTTTTTGTAGAG	84900
rs753377670	snp	A/G	0.000274081	0.0117032	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833921	GGCGGGGTCCTGATC[A/G]TTCTCTACAGCCTCT	84900
rs753415287	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116764887	ACAAGAGCGAAAGTC[C/T]GTCTCAAAAACAAAC	84900
rs753476442	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116846548	TCCTGCCTTCGCCTC[C/T]CAAAGTGCTGGGGTT	84900
rs753499386	in-del	-/ATA			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738944	TTGAAAAATATTTAT[-/ATA]ATGACCTTTTCTTGA	84900
rs753510798	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116834943	CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT	84900
rs753511699	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116847532	TTTCTCTCTCTCTCT[-/C]TTTTTTTTTTTTGAG	84900
rs753512280	in-del	-/TCT			intron-variant	RNFT2	GRCh38.p7	12:116788440	TCCCTCTTTCTCATG[-/TCT]TGATAACTCCTGTTC	84900
rs753538771	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116793526	ATGTGTTGCATTTGC[C/G]TGGCCTGGCTCCTAC	84900
rs753546220	snp	C/T	9.28807e-05	0.00681408	missense, intron-variant	RNFT2	GRCh38.p7	12:116849423	GGAAGGACGGCGCCA[C/T]GTCCGCACACTTCCA	84900
rs753551304	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116805276	AGTTCTCTCTTTTTC[C/T]TAATCTTGATGGGAG	84900
rs753564245	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116764047	GAATTAATGGAATTC[A/G]CAGCAACCTGGATGG	84900
rs753581472	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116797538	CAGCCTGTCTATCTC[-/A]AAAAAAAAAAAAAAA	84900
rs753600365	in-del	-/A/AA			intron-variant	RNFT2	GRCh38.p7	12:116827219	GTGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA	84900
rs753600786	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116847982	ATGCATTAGCAATTT[A/T]TCCTGATGTTCTCCC	84900
rs753628730	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116806680	AGCCTGAGAGTTCGA[A/G]GCTGCAGTGAGCCAT	84900
rs753636513	snp	A/G	3.31312e-05	0.00406995	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766906	CAGCTCCCAGCAGCT[A/G]TACAACAGGTGAGCA	84900
rs753665307	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816259	CTGGGGCACGTGCGC[C/T]GGGCCCTTCCTGTTC	84900
rs753704727	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773355	GGTTACTAACTTAAG[C/T]AAACAGGGAATTCTT	84900
rs753706898	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116786475	GATGACAGCACAGGT[C/G]TTTACAACTTCAAGA	84900
rs753827140	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116785118	CCTCCCTCCTGTCTC[A/G]GCCTCTTGCACATGC	84900
rs753889956	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116757243	AATCTTGCTAATGGT[C/G]TATCAGTTTTATTTA	84900
rs753895288	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813143	TTTGTATTTTTTGTA[A/G]AGACAGGGTTTTGCC	84900
rs753961085	in-del	-/AGAGAGAGAG			intron-variant	RNFT2	GRCh38.p7	12:116841959	TATAAATATATATAT[-/AGAGAGAGAG]AGAGAGAGAGAGAGA	84900
rs754004611	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116851627	TGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTAA	84900
rs754032721	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116747939	CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG	84900
rs754044663	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778203	AAACTAGAGGGGACT[A/G]TTATGGTTGGGTTTG	84900
rs754058414	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116837383	ATTCATGCAGTGTCT[C/T]GGGGGACTGAGGCAG	84900
rs754070295	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746656	ATGATGAGAAAGGGG[C/T]ACATGATAAGATTGG	84900
rs754088192	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116839067	CTTCCTCCATAAAGT[C/G]TTTCCTGACTCTGCT	84900
rs754117493	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801025	GTGTATTTATCCACT[A/G]TGTGAAGTGCTTTAT	84900
rs754120178	snp	A/C	6.70803e-05	0.005791	intron-variant	RNFT2	GRCh38.p7	12:116740541	CACGTCTCCAAGAGA[A/C]TTTGCATCTTTATTA	84900
rs754120854	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116831034	TTCCCTTTGTCTTTC[A/C]TGATCTTGACATTTT	84900
rs754208596	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759831	CGCTATTTTTGTGCT[A/G]GTTGGCCTCCTGCCA	84900
rs754209218	snp	A/G	3.12241e-05	0.00395109	intron-variant	RNFT2	GRCh38.p7	12:116750318	GCTCGGTGAGTTCTG[A/G]GGGCATGGGTGTCCT	84900
rs754222060	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116787997	CAATGGCGCAATCTC[A/G]GCTCACCACAACCTC	84900
rs754254462	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116812826	GGTGTGAGCCACTGC[A/G]CCTGGCTAGGGCTGT	84900
rs754284223	snp	C/G	1.64795e-05	0.00287045	intron-variant	RNFT2	GRCh38.p7	12:116835957	ACCCTGCTCTCCTTT[C/G]AGTCCTTCGACATCT	84900
rs754289496	in-del	-/A/AA			intron-variant	RNFT2	GRCh38.p7	12:116775265	ACTCCCGTCTCAAAA[-/A/AA]AAAAAAAAAAAAAAG	84900
rs754320226	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116843779	CTCTGAGGAAGGGAT[C/T]GTGAGCTCCCGGAGG	84900
rs754325543	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116799814	GATGAAAATGATGGC[C/T]TGGATAATTAGGGGT	84900
rs754337669	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800631	AGAGCAAGACTCTGT[A/C]TCAAAAAAAAAAAAT	84900
rs754374099	snp	A/C	1.65209e-05	0.00287405	intron-variant	RNFT2	GRCh38.p7	12:116836068	AGGGTCCTGAGAATC[A/C]GGAACTGGAAACAGC	84900
rs754399587	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116833351	CATTCTGTGCCCATC[C/G]TGCCCAGGCCCCTGA	84900
rs754415647	in-del	-/AAG	0.000142116	0.0084284	intron-variant	RNFT2	GRCh38.p7	12:116851761	AAAAAAAAAGAAAGA[-/AAG]AAGGGAGGGAGGGAG	84900
rs754435808	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116766724	CTTCAAAATGTTGAC[-/A]AAGTGAAAAGCTGCC	84900
rs754478535	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116748050	CAAAAATTAGCCGCA[A/C]ATGATGGCAGGTGCC	84900
rs754486519	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779231	CCTGGAGATGCTGGA[C/T]TTCTTTGACCTGCTA	84900
rs754492550	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116846234	TAGTTATAGAGCACT[A/T]ACTATTTGCCAGTCA	84900
rs754525065	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831599	GCACATCTTTGCACC[C/T]ATCTCTGATTATTTT	84900
rs754533298	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116767439	GCCCAGGCTGGGCTC[C/G]GACCTCTGAGCTCAG	84900
rs754542093	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116790946	AGCCTAGGCAACAGA[C/G]GGAGACCCTGTCTGA	84900
rs754576344	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116802776	CTCAGCATGTGGCAA[C/T]TTCCTACAGGAGCTA	84900
rs754675543	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116783922	CTGGCCACTGTCCCA[A/C]GTACTTTACATGTAC	84900
rs754679581	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813167	TTTTGCCATGTTATC[C/T]AGGTTGGCCTTGAAC	84900
rs754745498	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116788522	GGTGTGGTGCTCCCA[C/T]GAGGACTCCTACAGC	84900
rs754765081	snp	A/G	0.000116191	0.00762116	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116741074	CCACAGCAGCAACAC[A/G]GATAACATTCCACCT	84900
rs754770584	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116813992	GATCACTACAGCTTA[-/G]TAAGTGCTAGGCTCG	84900
rs754800002	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116796963	ATCATTTTTAGTTGG[C/T]ACCATTGGAGGGGGT	84900
rs754850762	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116740122	AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC	84900
rs754852805	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753737	CTGCACAGCCCATCC[C/T]CTGATCCAGTGCTAT	84900
rs754857020	snp	A/G	0.000263539	0.0114761	intron-variant	RNFT2	GRCh38.p7	12:116748655	TCTGCCGCCCACCCA[A/G]TGTCAGCTGTGACCA	84900
rs754857107	snp	C/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779324	CGTGGCCCTGCCCAA[C/G]ATCATCCTGGCTGTC	84900
rs754922726	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116796249	TAAGGTTATCATAAG[G/T]TGCAAGGTCAGGTAT	84900
rs754947352	snp	C/T	0.000680714	0.0184362	intron-variant	RNFT2	GRCh38.p7	12:116766929	GGTGAGCATGGGAAT[C/T]CAACCCCCACGGTGG	84900
rs754958360	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774715	GACTCAGTTCTGAGG[C/T]GTCAACACAGATCTC	84900
rs754963175	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116822626	CCACCTGCAGTGAGT[C/T]CAACCTTGGCAGGAG	84900
rs755025888	snp	C/T	1.79094e-05	0.00299239	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737804	CCTGCTTGAAGGTGC[C/T]GCTGAGGAAGTAGAC	84900
rs755045547	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116816521	GGGGTGAGAGGGAGA[A/G]AATGACACATTTTCA	84900
rs755102246	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116745000	GAAAAAGCTCAAGGC[C/T]CCTTGAGGATCATAG	84900
rs755175596	in-del	-/GTGTGTGG/GTGTGTGTG			intron-variant	RNFT2	GRCh38.p7	12:116785274	TGTGTGTGTGTGTGT[-/GTGTGTGG/GTGTGTGTG]GGCGGGGGGGGGTTG	84900
rs755182220	snp	C/G	3.30098e-05	0.00406249	intron-variant	RNFT2	GRCh38.p7	12:116753945	GGCTAGGCCTGATGA[C/G]TCTAAGTGGGTGACA	84900
rs755189143	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116826370	TGCAACAATTGCTAC[C/T]GTTTCCCCTTCACGG	84900
rs755200093	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781754	CTCTTTTGCCACAGA[A/G]GGTAACATTCACAGG	84900
rs755220130	snp	C/G	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754027	CACCTTCGCCTATGC[C/G]AACTCCACGCTTCGA	84900
rs755224892	snp	C/T	5.86631e-05	0.00541554	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836271	CGAGAGCCTCTGATT[C/T]TCCTGTGCCAGGTGA	84900
rs755233086	in-del	-/G	2.11611e-05	0.00325271	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737770	AAGGGAAGGGGAGGA[-/G]GGGAAGGGCGGCCAC	84900
rs755257919	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757448	TTCAGTCTTTTTGAT[A/G]TAAGCATTTAGGGCT	84900
rs755312940	in-del	-/TGGATGGATGGGATGGGTGGGTGGG			intron-variant	RNFT2	GRCh38.p7	12:116839400	GGGTGGATGGATGGA[-/TGGATGGATGGGATGGGTGGGTGGG]TGGATGGATGGGATG	84900
rs755326859	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116798087	AGGACGGGCCCTGGT[C/T]CAATAGGACTGGTGT	84900
rs755340882	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768290	ATTTTTCATAGAGAT[A/G]GGGTTTCACCATGTT	84900
rs755353566	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810819	TGCTTTTTGCTTCCA[C/T]TGGGGTAGGGGGGAC	84900
rs755366975	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839686	GGTATAAGTGGGTGA[A/G]TGACAGTGTGGGTGA	84900
rs755371606	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737433	GGAGGAGGACGGAAG[A/G]AGGAAGGGAAGGAAG	84900
rs755376898	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780434	CTCCTAGGAGAATCT[A/G]CTGCCGCAGCTGATC	84900
rs755383787	snp	C/G			downstream-variant-500B	RNFT2	GRCh38.p7	12:116853690	AGTGCAACTGTCTTA[C/G]ATCAAAGGAGAAGAA	84900
rs755410229	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820139	TGTGTCTCCCAGGCT[A/G]GAGTGTAGAAGTACG	84900
rs755410798	snp	C/T	0.00014871	0.00862165	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750072	CCGGGGCGAGGGGGG[C/T]GCCTACCACCACCGC	84900
rs755451870	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809926	ATGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	84900
rs755502576	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800647	TCAAAAAAAAAAAAT[A/G]GTTTAAAAATGCAAA	84900
rs755530790	snp	A/G/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736676	TGGGTGCACCCTGGG[A/G/T]TGTAACCACCCTTTC	84900
rs755593155	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116846538	CGAGCCATCCTCCTG[C/T]CTTCGCCTCCCAAAG	84900
rs755600041	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810018	GAGGAAACCAAGTCC[C/T]CAAAGTGACCAGTTC	84900
rs755621855	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116834774	ACCCTAATTTCTCAC[C/T]TATGAAGCTCACCAT	84900
rs755648353	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116843960	GGCTGCCCTCATGGC[A/G]TTTACCACCTAGAGG	84900
rs755661370	snp	A/G	6.22995e-05	0.00558085	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749899	GGTGGCGTCTTTGAG[A/G]GTCTGAAGGCAGAGG	84900
rs755682653	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750569	AAACTTCCTCGCTGG[A/T]TGGCTGGTGTAAAGG	84900
rs755704514	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116792013	CTGAATTATTAGACC[A/G]CGGTCCTTCCCGTGT	84900
rs755725113	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116762755	TAGCTGAGATTACAG[A/G]TGCATGCCACCATGC	84900
rs755746609	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833477	CTTCCAAGCCACAGC[A/G]AGACCCAGAGGGTGA	84900
rs755771082	in-del	-/TC			intron-variant	RNFT2	GRCh38.p7	12:116849800	CTTTTCTTTTCTTTC[-/TC]TCTCTCTCTCTGTTT	84900
rs755772557	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116749394	GTGATCCTCCCACCT[C/T]AGCCTCCTGAATAGC	84900
rs755773486	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116803874	TGAAAGGTTTTTGGC[C/T]CAAGGCAGTGGTGCA	84900
rs755797304	snp	A/G	1.64754e-05	0.00287009	utr-variant-3-prime, missense	RNFT2	GRCh38.p7	12:116852689	TTGGAGCTGGAGAAG[A/G]TTGATGAAAGTGCAG	84900
rs755801652	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116846305	TTAGACAAGGTCTCA[A/C]TCTGTCTCCCAGGCT	84900
rs755829226	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116802837	CAGTGGCTCATGCCT[C/G]TAATCCTAGCACTTT	84900
rs755829392	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116751560	AGGCAACCGCCACCA[C/T]ACCCAGCTAATTTTT	84900
rs755846321	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773270	CCCAGCCGCAAGTAA[C/T]GTCTATTGACACTTC	84900
rs755921068	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116845589	ATAAGCCATGGGTTG[A/C]AGGTCATGTGGCACG	84900
rs755928648	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815105	CATAAATGATGTAGC[C/T]GGTCCTAGTAGTAGT	84900
rs755947029	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804831	AATTAGCCAGGCATG[A/G]TGGTACATGCCTGTA	84900
rs755966868	snp	C/T	0.000127445	0.00798163	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750035	TCATCCAGATGCCCG[C/T]GTCCAGGGAGGAAGG	84900
rs755975744	snp	A/G	5.20494e-05	0.00510118	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849370	TGAGCGCACCTGCCC[A/G]CTCTGCCGCTCGGTC	84900
rs755976409	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116772672	CCAAAAACACCTCCA[A/G]TTCTGTCACCTAACA	84900
rs755983783	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814152	CCAGTCACCATGCAC[A/G]TACTACCTGCCAGCC	84900
rs756023703	in-del	-/T			downstream-variant-500B	RNFT2	GRCh38.p7	12:116854005	CTTCAGACTCTCCCC[-/T]AAGAGGCTCCAAGGG	84900
rs756028151	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741207	AGTTGTTAGAGTCAC[A/G]CTGATGGCCTCATAC	84900
rs756051079	in-del	-/GGGGCCCT			intron-variant	RNFT2	GRCh38.p7	12:116815058	TTAGTATGTCAACAA[-/GGGGCCCT]GCATTTTAATTTTAC	84900
rs756062185	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116748834	GAGTCGGCCTGGGTT[C/T]GAATCTCCCCTGCTC	84900
rs756083120	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771785	AGCACAGGAAATTGA[A/G]TGGATTACTTAGCCC	84900
rs756086557	in-del	-/GGCGCGGACGTGGGGCGCGGCGGCCGG	4.65951e-05	0.00482653	upstream-variant-2KB, cds-indel	RNFT2, C12orf49	GRCh38.p7	12:116737904	CAGGTTCACCATCCC[-/GGCGCGGACGTGGGGCGCGGCGGCCGG]GGCGCGGAACGCGGC	84900
rs756144219	in-del	-/AAAA			intron-variant	RNFT2	GRCh38.p7	12:116827220	GTGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAGAAA	84900
rs756168878	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116824252	GCTCTCTATGAGCCA[C/T]GCCTATGGGAAACCC	84900
rs756190117	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116777009	TGCAACCTCTGCCTC[C/T]TAGGTTCAAGTGATT	84900
rs756224776	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746605	GTTAGGGGAGACATC[C/T]GGTGAAGGTGATAGC	84900
rs756246780	in-del	-/AAAG	0.00202928	0.0317887	intron-variant	RNFT2	GRCh38.p7	12:116851752	TCTGTCTAAAAAAAA[-/AAAG]AAAGAAAGAAGGGAG	84900
rs756282127	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829542	TTCTTGGTCCTTGGT[A/G]GATGTGGGTGTACGT	84900
rs756285750	in-del	-/CTTTTGTGTCTGG			intron-variant	RNFT2	GRCh38.p7	12:116791234	AATACCCTATGTGGC[-/CTTTTGTGTCTGG]CTTCTCTCATGCCGT	84900
rs756356494	snp	C/T	6.44641e-05	0.00567696	intron-variant	RNFT2	GRCh38.p7	12:116766791	GCACCTTTGATATCA[C/T]ATATCTCTTGCTTTG	84900
rs756398598	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116758174	GTGTCCATTTGCATG[-/A]AATGCCTTTTTCCAC	84900
rs756441563	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116826418	AGCTCATAATCTGAT[C/T]GTATTCCTTGTTCTC	84900
rs756447648	snp	A/G	2.75251e-05	0.00370969	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750201	CGAGCAGCCTGGGAC[A/G]CCCGCCCCCGCCCTG	84900
rs756519580	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116769920	GGATCCTGTAATCCC[A/C]GCTACTTGGGAGGCT	84900
rs756530774	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842392	TCTGCCTCTCACATG[C/T]CCGAGGTTGGATTCC	84900
rs756545564	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810861	CATATTTCCCCCAGA[C/T]GTTTCTCCTTCCCTG	84900
rs756568410	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116841273	CCTAAGCAACATAGC[A/G]AGACCCCCATCTCTA	84900
rs756587035	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116743352	GCTCACTACAACTTC[C/T]GCCTCCTGGGTTCAA	84900
rs756618870	snp	C/T	3.79384e-05	0.0043552	intron-variant	RNFT2	GRCh38.p7	12:116833968	CCAAGGCTGGAGGGC[C/T]GGCCTAAGGAGGGCC	84900
rs756645163	snp	C/T	1.64811e-05	0.00287059	intron-variant	RNFT2	GRCh38.p7	12:116835950	AGCCACCACCCTGCT[C/T]TCCTTTCAGTCCTTC	84900
rs756650185	snp	A/C			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852784	TTACTTTGGGAAGTC[A/C]CTCAGCCTCCCTGTA	84900
rs756675091	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116740783	CGCGTTATCCTCTCA[C/T]ATGAGGACTTTCTCC	84900
rs756707098	snp	A/T	5.1577e-05	0.00507797	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750137	GCGGGGGCTCCCTGC[A/T]GCAGCACGTGGGTGG	84900
rs756720179	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811804	TGCTGGCCTCTGGCT[C/T]TTCTCCTCGGGGCCC	84900
rs756754753	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799192	TCACTCTCAGCTCCT[A/G]GAAGCCACGCTCCAG	84900
rs756776691	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116822301	GAAGCAGGGCCATCA[G/T]TTTGGCAAATGGCCC	84900
rs756785220	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116841289	AGACCCCCATCTCTA[C/T]AAAAAATACAAAAAT	84900
rs756786611	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116843386	TAGTCGAGCTACTCA[-/G]GAGGCTGAGGTGGGA	84900
rs756793459	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804587	CACTACATATGCACA[A/G]AAGTTTCTCTAACAC	84900
rs756812845	snp	C/T	0.00014403	0.00848494	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749936	CCCCACCAGCGCTCT[C/T]CTCGGGCTTATCAGG	84900
rs756820758	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739857	AAAACATATTTTCTG[A/G]CTTCCCCAATCAGGA	84900
rs756907013	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116748383	TCCAACCCAAGAGGC[C/G]CTTGCTTGGAACTAG	84900
rs756907208	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116834953	CTCCCGGGTTCAAGC[A/G]ATTCTCATGTCTCAG	84900
rs756922767	snp	A/G	1.65485e-05	0.00287645	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833864	ATCCAGCTGTGGTAC[A/G]AATACATCATGGGTG	84900
rs756975373	snp	A/G	1.7904e-05	0.00299193	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750056	GGGAGGAAGGAGGGG[A/G]CCGGGGCGAGGGGGG	84900
rs757033770	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116848067	TGTTCTCATTGTTCA[G/T]CTCTGATTTATGAGT	84900
rs757041523	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116793605	GGACCAGCCATGCTG[A/G]TGACTTCTTGGTGCC	84900
rs757048916	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749565	GATTACAGGCATGAG[C/G]CACTGCATCAGCCCT	84900
rs757088438	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116769689	GTACCAAGTAAAAAT[A/G]TTACAGTAAGCTAAG	84900
rs757091299	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116774471	AGAGATCACTGCATA[A/C]GCGAATGCTAATCAG	84900
rs757158125	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116846617	TTTTGCTTTTAAAAA[A/C]ACATTTTGTTTAGAT	84900
rs757171985	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804291	CCTGGCAACTTGTTA[A/G]AAATGTAAAGCCTCA	84900
rs757209679	snp	C/G	5.1202e-05	0.00505948	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766819	TTGTCTTCAGGAGAA[C/G]AGGTCAGTGCTGGTC	84900
rs757254451	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753898	TGAGGGGACCAGGGA[C/T]GTGCCTTTTCCCCCA	84900
rs757257179	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116797026	GGTGCTGCTGAATAT[A/T]CTACAGTGCACAGGA	84900
rs757286866	snp	A/G	0.000136423	0.00825788	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849424	GAAGGACGGCGCCAC[A/G]TCCGCACACTTCCAG	84900
rs757310299	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116838279	CCAACCTGGGCCCAT[C/T]GTGTTGATTAAAGGT	84900
rs757334013	snp	C/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835961	TGCTCTCCTTTCAGT[C/T]CTTCGACATCTGTGG	84900
rs757335196	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808275	TTAAGTTTTTTATAG[C/T]AACGGGGTCTTGCTG	84900
rs757352417	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116830767	ATACAAAAATTAGCC[C/G]GGCATGGTGGTGTGT	84900
rs757493503	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116792651	GTGATGTGAATAGTC[-/T]TCCCCAAGATAAATT	84900
rs757532990	snp	A/G	1.92832e-05	0.00310504	intron-variant	RNFT2	GRCh38.p7	12:116833974	CTGGAGGGCCGGCCT[A/G]AGGAGGGCCCCATTC	84900
rs757579637	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116790422	TAATCTTAACAGTCC[A/C]AGGAGGGTAGATGCT	84900
rs757582809	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778234	TCCCCAGCAAAACTC[A/G]TGTTGAAATTTGATC	84900
rs757584423	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116765657	TTTCCTAGGATTGCT[C/G]TCAGGCTATGAAACT	84900
rs757589942	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817735	TAGAAAGTATGGAGT[A/G]AGACCACACTTTACA	84900
rs757603857	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116740229	CACTGAGAGGCTACC[C/T]AGAGATACTGAGCAG	84900
rs757676784	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116797771	CCCATAGGCAGAGAG[C/T]AGCACCTCAGGGCAA	84900
rs757679050	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799970	CGTGGTACCCTCCCC[A/G]AGGTGATGAGTGAGT	84900
rs757687391	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116828603	CTCCAGAACCTGGCA[C/T]TGTGTCTGGTGCATA	84900
rs757689527	in-del	-/AGGG	0.00255355	0.0356406	intron-variant	RNFT2	GRCh38.p7	12:116851764	AAAAAGAAAGAAAGA[-/AGGG]AGGGAGGGAGGGAGG	84900
rs757710906	snp	C/T	2.53264e-05	0.00355845	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750208	CCTGGGACGCCCGCC[C/T]CCGCCCTGTCCGAGC	84900
rs757713066	snp	A/T	1.65239e-05	0.00287431	intron-variant	RNFT2	GRCh38.p7	12:116836072	TCCTGAGAATCAGGA[A/T]CTGGAAACAGCAGCG	84900
rs757721361	snp	A/G	0.00013449	0.0081992	intron-variant	RNFT2	GRCh38.p7	12:116851855	GTCTCCTGTCTTTAT[A/G]TCTTTCTCCTCTTCC	84900
rs757757260	in-del	-/AGAA			intron-variant	RNFT2	GRCh38.p7	12:116822707	AAGAAGAGGAGAGAT[-/AGAA]AGAAAGAGAACTGGC	84900
rs757770957	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116787719	TGTTGTCTCTAAAAG[-/AA]AAAAAAAAAAAAAGA	84900
rs757802985	snp	A/G	0.000160418	0.00895452	intron-variant	RNFT2	GRCh38.p7	12:116750319	CTCGGTGAGTTCTGG[A/G]GGCATGGGTGTCCTA	84900
rs757823752	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116843839	TCGCCAGACTTTCCT[A/G]TTTGGTCATTTGTCA	84900
rs757835519	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116801348	AAATGTACCTCCCTT[C/T]CTGTTGCCAGGAAGA	84900
rs757868345	in-del	-/AGG			intron-variant	RNFT2	GRCh38.p7	12:116847619	GCAACCTCTGCCTCC[-/AGG]AGGGTTCAAGTGATT	84900
rs757908341	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116787720	GTTGTCTCTAAAAGA[-/A]AAAAAAAAAAAAAGA	84900
rs757911142	snp	A/G	3.66186e-05	0.00427878	missense, intron-variant	RNFT2	GRCh38.p7	12:116849440	TCCGCACACTTCCAG[A/G]TGTACTAGGACCGAA	84900
rs757932414	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116821450	GCAGGACTCTGCCAG[C/G]TGTGGTCCCCACAAC	84900
rs758000777	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116740769	GCTGCACAGTTTACC[A/G]CGTTATCCTCTCACA	84900
rs758004335	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116740012	GAAGTTTGAGACCAG[C/T]CTGGCCAATATGGTG	84900
rs758039300	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116823588	ACTCTGGTGGCTGAG[G/T]CAGGAGAATTGCTTG	84900
rs758063499	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796054	GCTGATATTACAGGC[A/G]CCCACCACCACACCC	84900
rs758099589	in-del	-/AAAA			intron-variant	RNFT2	GRCh38.p7	12:116743082	TGAGACCCTATCTCA[-/AAAA]AAAAAAAAAAAAAAA	84900
rs758148878	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782721	ACATCCCTGGGAAGC[A/G]GGCACTGTTATTCCT	84900
rs758156228	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116752229	TTCGAGAGGAGATGA[A/G]ACCATTCTTTATTTC	84900
rs758189753	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116744546	AGGAAGTAGCAGGGC[C/T]GAGATTTGGGCCCCC	84900
rs758240428	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116765184	TGTCTTCCCAGAACA[C/T]TGCTAATTCCCTCTT	84900
rs758244446	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751219	CTGCCCCGGCCTACT[A/G]TATTTGTTATTAACA	84900
rs758308765	snp	A/G	5.06239e-05	0.00503085	intron-variant	RNFT2	GRCh38.p7	12:116741005	GTGGGAGTGTTGGGA[A/G]ACTCTGGCTCACCCA	84900
rs758333680	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116805585	GTTCCAGCAAGTCTC[A/G]TGCCTCAGCCTCCTG	84900
rs758366985	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116764246	AAGACTACAAATTGG[G/T]TTCAGTGTATACTGC	84900
rs758398786	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849620	CTGACCTTCATCTTC[C/T]TCTCTCGTTCTGTGG	84900
rs758420558	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849613	TGTCCTTCTGACCTT[C/T]ATCTTCCTCTCTCGT	84900
rs758422059	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809044	CTGGATGCACAGGGC[C/T]GGAGCCATGGCTTTT	84900
rs758432803	in-del	-/ACTTACTTTGC			intron-variant	RNFT2	GRCh38.p7	12:116768078	CACTGGAGATCAGAA[-/ACTTACTTTGC]ACAGTTTGGCCTTTT	84900
rs758449957	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848209	GCATAGTATTCCATG[A/G]TGTATATGTACCACA	84900
rs758490172	snp	C/T	1.69375e-05	0.00291006	intron-variant	RNFT2	GRCh38.p7	12:116750356	GGCTTCACAGGCAGG[C/T]TGCCTGCAGCCGGTG	84900
rs758529808	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809729	TCAGGTTGGAGCACA[A/G]TGGCACAATCTCAGC	84900
rs758621090	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116797169	TATGGATTGAACTGT[C/G]CTCCCCGAATGTTAT	84900
rs758705123	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116760202	ACTCCCACCATGCCC[A/C]CCACAACAGCCCCCA	84900
rs758754616	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736345	GAAGGGACAACACGC[A/G]ACTGTGAGGAGGTGT	84900
rs758770855	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116748020	ACGCGGTGAAACCCT[A/C]TCTCTCTAAAAATAC	84900
rs758774164	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116779445	AATGGATGAGGGTGG[A/T]CTGATGTCAGCATAT	84900
rs758783568	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116851795	AAGGAAGGAAGGAAG[C/G]AAAGAAAGAAAGGTC	84900
rs758818729	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116767271	GCATCACCCAGGCTG[C/G]CAGTGGTGTGATCAT	84900
rs758836217	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760964	GCTCATTGTAGCCTC[C/T]AACTCCCGGATTCAA	84900
rs758838986	snp	A/C	1.67402e-05	0.00289306	intron-variant	RNFT2	GRCh38.p7	12:116779375	CTGCGGCCACAAGGT[A/C]GCCCCAGTCACATGG	84900
rs758851409	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116818751	GTACAAGTCCCAGTT[C/G]TGCAGCAAGTAACTT	84900
rs758880896	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116845131	TGCCTATAGTTGTAG[A/C]TACTTGGGAGATTGA	84900
rs758932618	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746847	GGCTTTTAGTGGGAT[C/T]GTGAAATAATCAAAT	84900
rs758954992	snp	A/G	9.93789e-05	0.00704837	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737780	GAGGAGGGGAAGGGC[A/G]GCCACTGACCTGCTT	84900
rs758966561	snp	A/G	2.13623e-05	0.00326813	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737767	AAGAAGGGAAGGGGA[A/G]GAGGGGAAGGGCGGC	84900
rs758971508	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116781905	TACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	84900
rs758972837	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116817761	TTACACTCAAACAAA[A/C]CTGAGTTTTGAGCAG	84900
rs758984739	snp	C/T	3.295e-05	0.00405881	utr-variant-3-prime, missense	RNFT2	GRCh38.p7	12:116852657	GCCTGCAGATGCTGT[C/T]GAAGGGGCACAAGAA	84900
rs759016943	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116816055	CATTTGTGCTTAAGA[C/T]TATAGCTGACTTGGG	84900
rs759024210	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829909	AATTTAAACATATCA[C/T]ATGCTCAGTATAAAA	84900
rs759025561	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814881	ATGGTGTTTCACCTG[C/T]GTGCAAGCATGCCCA	84900
rs759040331	snp	C/T	1.64844e-05	0.00287087	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852723	TGTAAGGAAATAGAA[C/T]AGTCTGCTGGGAGTC	84900
rs759108220	in-del	-/CTTT			intron-variant	RNFT2	GRCh38.p7	12:116778134	TTCTTTTCTTCCCTC[-/CTTT]CTTCCTTCCTTCCTT	84900
rs759111821	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774218	GGTCTGTGGTTGGAT[A/G]GTGGTGATGATTATG	84900
rs759149103	snp	A/G	8.86918e-05	0.00665868	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836235	GCTGGTGACATCTGC[A/G]CCATCTGTCAGGCCG	84900
rs759158631	snp	A/C	4.94531e-05	0.00497234	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116753985	TCTCTGTCCCACAGG[A/C]ATTGCTGTGTGCATC	84900
rs759165521	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116827507	ATGTGTTAGAATCCC[-/C]ATCGTGACTTATCTA	84900
rs759167444	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773162	GAGACAGGTTTCACC[A/G]TGTTGGCCAGGCTGG	84900
rs759186517	snp	C/G	2.89876e-05	0.00380696	intron-variant	RNFT2	GRCh38.p7	12:116750312	GCATAAGCTCGGTGA[C/G]TTCTGGGGGCATGGG	84900
rs759237267	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116742137	AGAGGGCAGAAAGGA[A/C]CGAGGAAAAAGCATA	84900
rs759262928	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116829962	CAAAGAGAATGAGGA[-/T]TTTTTTTTTTTTGCA	84900
rs759279763	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116832309	AGTATAAACCAGAAT[C/T]ATACAACAAATATTC	84900
rs759312702	snp	C/T	0.000117336	0.00765862	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750015	GGCTGGCGGCGGGGA[C/T]GTGTTCATCCAGATG	84900
rs759346903	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736960	GGGCTGGCCGACCCT[C/T]GCCACCTATGTCTTG	84900
rs759352198	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116840373	CCGTTGTTCCTCAGT[A/C]ACAGAACCAGGATTC	84900
rs759368012	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116744571	GCCCCCATCCCTGTG[-/T]CCCCCAGCACCTGTG	84900
rs759375442	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853270	TAAGTAGGGTTAATC[A/G]AGTATCAGGTTCACA	84900
rs759379827	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116777811	CTTCCAGAGATAACT[G/T]TATTTGCCCAGAGTC	84900
rs759395882	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116779182	CTTCTGACTCTCTCA[A/G]TCCTCCCCCCAGCCT	84900
rs759434754	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116748532	TATTCAGGAATAAAG[G/T]CCCATTTTTCAGGTG	84900
rs759434849	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800199	AACCTCTTTTCTTTA[A/C]AAATCACCTAGTCTC	84900
rs759445486	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116819680	CCGCCCCGCTGGCCC[C/T]GCCTCCTACCTGCTG	84900
rs759507233	snp	A/G	1.65083e-05	0.00287296	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833827	CGAGGAGCTGAGCCA[A/G]CTGTTCCGATCCCTT	84900
rs759618808	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116758702	CCCAATCCCTTCTAG[C/T]TTGTAGGGTTTCTGC	84900
rs759652278	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116774936	CTGGTGCACAGAAAG[-/AG]AGAGAGAGAGAGAGA	84900
rs759657174	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116759617	TGAGCCAAACTGCAG[A/T]GATTGTTGTCTGTCT	84900
rs759667232	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116842765	TTTTAGTAGGGACGG[A/G]GTTTCGCCATGTTAG	84900
rs759684250	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116769902	TAGCCAGGTGTGGTG[A/G]CAGGATCCTGTAATC	84900
rs759686857	snp	C/T	3.44364e-05	0.00414934	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750097	CACCGCCAGCCCCAC[C/T]ACCATTTCCACCATG	84900
rs759690045	in-del	-/TG			intron-variant	RNFT2	GRCh38.p7	12:116750788	ATTATTTTTACTATA[-/TG]TGTGTGTGTATATAT	84900
rs759695696	in-del	-/CTC			intron-variant	RNFT2	GRCh38.p7	12:116797735	ACAGCACCGTGACTA[-/CTC]CTCCTGCAGAGCAGG	84900
rs759735061	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116839180	CTAGGTAGTTCATTT[G/T]GTAATTAGATGGGCA	84900
rs759755039	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116770979	TTTTATTAGTAACAT[C/T]TTGCTGAAACACAGC	84900
rs759758162	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799645	AAGGATTTTTTAAAG[A/G]GATTCCTCAGCTGGG	84900
rs759760459	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116781960	AGCATGCGCCTGTAG[C/T]CCTACTTACTCGGGA	84900
rs759779705	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116821980	GCTGAGATTACAGGT[A/G]TGCACCTCTACACCA	84900
rs759821379	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116762271	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	84900
rs759828459	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835587	GCATACTGATTACTT[A/G]CTGGTTCTGATCAAC	84900
rs759881869	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738632	AAAAGTCTCGGTGCG[A/G]TCCTTCAAAGGGACA	84900
rs759919442	snp	A/G	0.000173333	0.00930786	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766875	CGGGGAACACCCTCT[A/G]TGTGCTTTATACATT	84900
rs759938322	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116794295	ATTAATGATCTATTA[G/T]AAGGTTTAAAACCAG	84900
rs759951069	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116801654	TAAGAGCATTAGCAG[A/C]CATCTGTTTATAATT	84900
rs759957234	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820973	TCCCACTCTGTTCTT[C/T]CCTCCCCTGCCTCTG	84900
rs760030095	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116848943	CTTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	84900
rs760114418	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116804915	GAGGCTGCAGTGATC[C/G]ACGATTACACCACTG	84900
rs760162727	in-del	-/AAG			intron-variant	RNFT2	GRCh38.p7	12:116827233	TCAAAAAAAAAAAAA[-/AAG]AAAGAAAGAAAGAAA	84900
rs760191484	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116776350	ATAAGTCAGATCTTC[A/C]TTTGATCATGATCAT	84900
rs760268690	snp	A/C	1.79236e-05	0.00299357	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737853	CAGGGCGAGCACCCA[A/C]CTCTTCCGCAGAAGC	84900
rs760297194	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116822459	CCAGCTGCGTCACCT[-/G]GGGGCAGGTTATCTA	84900
rs760324919	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763959	AACCATCCCAAATGC[C/T]CATCAACCAATGAGT	84900
rs760331993	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116817079	ATACAGTGGTGCGAT[C/T]GCAGCTCACCGCAAC	84900
rs760378408	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774290	AAAAATGGTTAAGAC[A/G]GTACCTTTTATGTTA	84900
rs760383329	snp	A/G	3.89188e-05	0.00441111	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750165	TGGGGACCACCGGGG[A/G]CACTCGGAGGAGGGA	84900
rs760424851	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775728	CATATATCACAATTA[A/G]TATGATTCTTTTACG	84900
rs760477970	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116798662	CAACCTCAGCCTCCC[A/C]GGCTGAAGTGATTCT	84900
rs760509242	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116758014	GAGCTCCAGTGTTAG[A/G]TGCATATATATTTAG	84900
rs760531519	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116841673	GAGTCACTGGAACCT[A/G]GGAGGCAGAGGTTCC	84900
rs760556718	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116826098	AGTCTTCAAATCATC[C/T]TTCCCATGTAGGTGC	84900
rs760621547	snp	G/T	1.69132e-05	0.00290797	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833912	TACTTCCTGGGCGGG[G/T]TCCTGATCGTTCTCT	84900
rs760630700	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832349	TGTCTTCTTTGATTC[A/G]ACATAATGTTTGTGA	84900
rs760646503	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116769578	AATAGGAAAAACCTT[A/T]TAGAATAAGGATATA	84900
rs760700175	snp	A/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739294	ACAGGGAGCAAGGGA[A/T]CTAGAAAAGGGGAAC	84900
rs760717481	snp	A/G	0.000144571	0.00850087	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750110	ACCACCATTTCCACC[A/G]TGGCGGCCACCGCGG	84900
rs760758657	snp	A/G/T	4.96882e-05	0.00498414	missense, intron-variant	RNFT2	GRCh38.p7	12:116849419	TGCTGGAAGGACGGC[A/G/T]CCACGTCCGCACACT	84900
rs760767251	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116782728	TGGGAAGCGGGCACT[A/G]TTATTCCTACCACCC	84900
rs760770810	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116800635	CAAGACTCTGTCTCA[-/A]AAAAAAAAAATGGTT	84900
rs760798541	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116747913	GATGAACCCTCGGCC[A/G]GGCACGGTGGCTCAT	84900
rs760822290	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791507	GAGAGATGGGGTTTC[A/G]CCATGTAGGCCAGCC	84900
rs760822677	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116831015	AACCTCACACTCCTT[C/G]GTCTTCCCTTTGTCT	84900
rs760824501	snp	C/G	1.64846e-05	0.0028709	intron-variant	RNFT2	GRCh38.p7	12:116779190	TCTCTCAATCCTCCC[C/G]CCAGCCTCATATTCC	84900
rs760843973	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116760736	TCCTTCAGAGAGTCT[C/G]TGGGTCCTCTCGGGA	84900
rs760846413	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801186	GGGTGCTGAGCCCAG[A/G]GGGTGCCCTGTCTGC	84900
rs760878870	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116812651	ACGGTTCTCCTGCCT[C/T]AGCCTCCTGAGTAGC	84900
rs760897001	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116772127	GACACAGTCTTGCTC[G/T]GTTGCCCTAGCTGGA	84900
rs760938508	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783099	ATGCCCATCTTTCCT[C/T]CTCCTACTGCTGCTA	84900
rs760945584	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116844863	GGTAGCATAGTTAAG[A/T]CCCATTTGGTTGGTC	84900
rs760969871	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116775260	GTGAAACTCCCGTCT[-/A]CAAAAAAAAAAAAAA	84900
rs761000327	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822976	CACTCCAGGTTGGGC[A/G]ATAGTGCGAGACTCT	84900
rs761005964	snp	C/T	3.58275e-05	0.00423231	intron-variant	RNFT2	GRCh38.p7	12:116849496	AAGGGTCAGCATGCC[C/T]GGACCCAGCCCTGCG	84900
rs761016977	snp	C/T	4.47057e-05	0.00472767	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766883	ACCCTCTATGTGCTT[C/T]ATACATTCAGCTCCC	84900
rs761021583	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771065	AATGGTTATGGCAGA[A/G]ACCATATAGCTTACA	84900
rs761050753	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800627	TGACAGAGCAAGACT[A/C]TGTCTCAAAAAAAAA	84900
rs761060893	in-del	-/AAAATATAT			intron-variant	RNFT2	GRCh38.p7	12:116806379	TCTCAAAAAAAAAAA[-/AAAATATAT]ATATATATATATAGA	84900
rs761103894	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820795	CCTCTCTCTCCTCAC[C/T]AGTTAACAGGGGCAA	84900
rs761137459	snp	A/G			utr-variant-5-prime, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740401	TGGAGACGAAGAGGA[A/G]GGGGAGGCCTGTCCT	84900
rs761156865	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811684	CCCGGCATGCGTGCG[C/T]GTGCGTTTGTGCATG	84900
rs761198941	snp	A/C	2.6e-05	0.00360546	intron-variant	RNFT2	GRCh38.p7	12:116741105	GAAAGGTAGGCATCC[A/C]TGCTTCTGTTCCATC	84900
rs761209951	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822097	GCCTCGGCCTCCCAA[A/G]GTGCTGGAGTTACAG	84900
rs761212567	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116782486	GAGCCATGATCGTGC[C/T]ACTGTACTCCAACCT	84900
rs761227605	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739744	GAATGGGAGGAAATG[C/T]AGTTGGAAACAGATG	84900
rs761227738	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116752898	ATAAACAGTAAGTGC[A/G]TCAGGTGAAAGAGGA	84900
rs761234553	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116769072	ACTTGTAAAAAATAA[-/C]AAGTTGGCCGGGCGC	84900
rs761277008	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823240	GGCCCAGAATGGCGG[A/G]GCTGGGTCAACACCC	84900
rs761286983	snp	C/G	1.67022e-05	0.00288978	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749844	CTTGGCACCCAGAAA[C/G]CGCAGCCAGGCGCTC	84900
rs761347103	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116838574	CAAGCCTCTTTTGAG[C/T]TTTGCCAATCTGACA	84900
rs761364209	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775377	GACACCAACAACCAT[C/T]ATCTTGGCCTCCTGG	84900
rs761368077	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116851172	CCCAGCCAGCATGGG[C/T]GGGCCAAGTTTCCAA	84900
rs761393244	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116796735	CCTTCCCTTCTCCCA[A/G]TCAGACATCTGTCTA	84900
rs761400237	in-del	-/C	3.2987e-05	0.00406108	intron-variant	RNFT2	GRCh38.p7	12:116779186	GACTCTCTCAATCCT[-/C]CCCCCCAGCCTCATA	84900
rs761448773	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795857	TATTCCCCAGGTAAC[C/T]TTGGCTGCTCTTTTG	84900
rs761515433	snp	C/T	0.000106028	0.00728029	intron-variant	RNFT2	GRCh38.p7	12:116851654	CTAAGGCAGGGAGAA[C/T]TGCTTGAACTCGGGA	84900
rs761558626	in-del	-/GAT			intron-variant	RNFT2	GRCh38.p7	12:116789944	GAGAGTGGATGGATG[-/GAT]GGTGGATGGGTGGGT	84900
rs761583829	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116788843	ATGGATGGATGGATG[A/G]ATGGATAAATGGGAG	84900
rs761643148	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116787347	TTGAGCAAGTCGCTT[A/G]ATGTGAGCATTTTCC	84900
rs761673093	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853625	TAAATACCATCTGTT[A/G]GTGCAACTTGTGTTT	84900
rs761686940	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799511	GGTGCCCACCGCACT[A/G]TCTCAGAGGGTTGTT	84900
rs761710513	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116842950	ATCCACCTGGACCCA[A/G]GCCTGGCTGCTTCCT	84900
rs761725722	in-del	-/TTTGTTTG			intron-variant	RNFT2	GRCh38.p7	12:116842569	TATTTTATTTATTTA[-/TTTGTTTG]TTTGTTTGTTTGTTT	84900
rs761729490	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116829041	CAAGACTCGCAGTTG[A/T]GAGAGGTTGGACAGT	84900
rs761745946	snp	A/G	3.61984e-05	0.00425416	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750171	CCACCGGGGGCACTC[A/G]GAGGAGGGAGGCGAC	84900
rs761769475	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116786524	GGAGTGGGTTTGGGA[C/G]AAGATAAGGAAGGCA	84900
rs761861083	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116762050	CCAACCCGGGTGACA[G/T]AGTGAGACTGTCTCA	84900
rs761861257	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116758148	AGAATAGCTACCCCT[C/G]CTTGCTTTTGGTGTC	84900
rs761887884	snp	A/C	2.06358e-05	0.00321208	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750265	AAAGGACTCCCCTTC[A/C]TCCTGATCCTCCTGG	84900
rs761940767	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800676	AAAAATTAGCTGGCA[A/C]TGTGGTGCGTGCCTG	84900
rs761941583	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116807392	ATAAATATCCAGTGT[-/C]CCTAGTACTGGTCTA	84900
rs761953430	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748676	GCTGTGACCAAGGCT[A/G]GCCCCTCTGGGGAAC	84900
rs761971306	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791684	GCCATTCCTCTGTCA[A/G]TGGACATCTAGGCTG	84900
rs761983753	snp	C/G	6.92593e-05	0.00588429	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749868	GGCGCTCAGCTCCGA[C/G]GCGAGTGTGGATGAA	84900
rs762013476	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116819869	CGACAGAAATATAAG[A/G]GTAGTCACACAGACG	84900
rs762013507	in-del	-/AAAAAAAAAAAAAAAAAAAAAA			intron-variant	RNFT2	GRCh38.p7	12:116743213	TACCAGGTAGAATCT[-/AAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84900
rs762039695	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761652	AAAATCATTTTTCTG[C/T]CATTTTCCCACTGAG	84900
rs762043905	snp	C/T	3.29582e-05	0.00405931	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852627	GCAACTGGTTTTTAT[C/T]GGAAAGATCATCCTG	84900
rs762083266	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116772997	CCACATCCAGCTAAT[G/T]TTTGTATTTTTAGTA	84900
rs762098067	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832771	CTGTTCATCTCCTTT[A/G]ATCCTCAAAGCAACC	84900
rs762154426	snp	C/T	0.00201362	0.0316663	intron-variant	RNFT2	GRCh38.p7	12:116849291	TAAAGAGTCCTGGTG[C/T]CTGCTGATTGCTGTC	84900
rs762179996	snp	G/T	2.77805e-05	0.00372686	intron-variant	RNFT2	GRCh38.p7	12:116741119	CCTGCTTCTGTTCCA[G/T]CTGAGGGCTCTAGGC	84900
rs762197284	in-del	-/GATG			intron-variant	RNFT2	GRCh38.p7	12:116789270	AATGGGAGAAGAGTA[-/GATG]GATGGATGGATGGAT	84900
rs762220902	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845852	AGCTATCTTCAAGTG[C/T]CTCAAACATCTTCCT	84900
rs762234429	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813692	ATGGTACATAGCAGG[C/T]ACTCAAAACACATAC	84900
rs762249650	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116818197	GCATGGTGGCACACA[-/C]CTGTGGTCCCAGCTA	84900
rs762264591	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845917	CCTGGAATGTTCTAT[C/T]TCTATCCCATCCCCT	84900
rs762289496	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824851	ACATTAGGGATTAGG[A/G]CTTCAACAAAGGAAC	84900
rs762342584	in-del	-/AAAAA			intron-variant	RNFT2	GRCh38.p7	12:116800859	AAAATAAAATAAAAT[-/AAAAA]CCATTTAACAGATAA	84900
rs762348769	snp	A/G	4.4961e-05	0.00474115	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836238	GGTGACATCTGCGCC[A/G]TCTGTCAGGCCGAGT	84900
rs762366073	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116741881	GCCTCAAACTCCTGG[C/G]CTCAAGCGATCTTCC	84900
rs762429112	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824971	AACCATTTAATTCTC[A/G]CAATTTTGCAGGTCA	84900
rs762429748	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754608	CATTCCCACCAGCAG[C/T]GTAGACGTGTTCCCT	84900
rs762455790	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116740594	TGGAAGGAAGTTTTG[A/G]TTTGACCACTCCACC	84900
rs762483049	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825802	ATGAAGAAACTGAGG[A/G]TCATAGAGGTTGAAT	84900
rs762535675	snp	C/T	2.55086e-05	0.00357122	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750300	ACTGTGCTTTCAGCA[C/T]AAGCTCGGTGAGTTC	84900
rs762592634	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783609	CACCCCTCCCTGTGC[C/T]CAGCTACAGCCAAGC	84900
rs762610225	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116791947	CATAGCTCACAAGTG[G/T]CTATGTGGAGATTTG	84900
rs762613920	snp	C/T	3.29761e-05	0.00406041	intron-variant	RNFT2	GRCh38.p7	12:116835941	GTACATTTCAGCCAC[C/T]ACCCTGCTCTCCTTT	84900
rs762673353	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736928	GCCCCCAAATTAAAC[A/G]AAGGGCACCCATGCG	84900
rs762700869	in-del	-/AAAAAT			intron-variant	RNFT2	GRCh38.p7	12:116806378	GTCTCAAAAAAAAAA[-/AAAAAT]ATATATATATATATA	84900
rs762706387	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116777950	CTTATTTATAAACTG[C/G]AGATAAGCAACACTC	84900
rs762714053	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116769977	GAGGCAGAGGCTACA[C/G]TAAGCCAAAATCGTG	84900
rs762714538	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116806984	CCTCTCCCTTTTTAC[A/G]TGGCTTCCCGGAAAT	84900
rs762734125	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766604	TTTCTAGATAGTTTT[C/T]CAAGCAGATGTCCAC	84900
rs762746332	snp	A/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779307	GCCCTCAAGTGCCTC[A/T]TCGTGGCCCTGCCCA	84900
rs762765019	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837747	ATCCAAATAGAGTCT[A/G]GAGTTGAGTTAATAG	84900
rs762793140	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818421	GCTCAGTGCCTGGTT[C/T]AGCACTGCCGTTCAG	84900
rs762804940	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778993	TTTAACTCTCAAGGG[A/G]ACTAAGACTCAGAGA	84900
rs762833947	snp	A/G	0.000140696	0.0083862	intron-variant	RNFT2	GRCh38.p7	12:116851771	AAAGAAAGAAGGGAG[A/G]GAGGGAGGAAGGAAG	84900
rs762842550	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116830846	GAGGCAGAGGTTGCA[G/T]CGAGCTGAGATTGTG	84900
rs762848830	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116851352	ACTACAGGCACACTC[C/T]GCTATCCCCAGCAGA	84900
rs762856543	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116817354	GAGGTCTCATGATGT[A/C]TCCCAGGCTAGTCTC	84900
rs762908924	in-del	-/GAG			intron-variant	RNFT2	GRCh38.p7	12:116841965	ATATATATAGAGAGA[-/GAG]GAGAGAGAGAGAGAG	84900
rs762940794	snp	A/G	1.64776e-05	0.00287028	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852630	ACTGGTTTTTATCGG[A/G]AAGATCATCCTGCCT	84900
rs762946401	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116747826	CCAACACATGCACGT[C/T]GAGCACATCGGCTCC	84900
rs762971761	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116842089	TCCTGGCTCAACTTG[A/G]GGAGGAGCTGCATCC	84900
rs762996549	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757393	CTTCTTGTTTCTCTA[A/G]TTCCTTGAGGGGTGA	84900
rs763003044	snp	G/T	4.34263e-05	0.00465954	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737763	AAGGAAGAAGGGAAG[G/T]GGAGGAGGGGAAGGG	84900
rs763032012	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746457	TCCTGTGCAGGTGAC[A/G]TGAGGGTGCAGTGAG	84900
rs763121208	snp	A/T			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738287	GCCGGAAGCATCGGA[A/T]GTCACATGCTGCCCA	84900
rs763132330	snp	A/T			missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750173	ACCGGGGGCACTCGG[A/T]GGAGGGAGGCGACGA	84900
rs763161435	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810715	CAATGATTAAGCAAG[A/G]CAGCCAGGCTCCCTG	84900
rs763193081	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794064	TGAGCCTAGGAGTTC[A/G]AGACCAGCCTGGCAA	84900
rs763242550	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116847278	GATGTCTCCAGTTGC[C/T]TTCAAAGTGCCCTTT	84900
rs763245573	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820750	CACCACTGTCTAGCA[A/G]CTTCGAACAACATAC	84900
rs763290339	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116819404	AGAGCGGGGCGGCCC[A/G]GGGCGCGGGGCTGTG	84900
rs763305705	snp	A/C	5.57916e-05	0.00528135	upstream-variant-2KB, missense, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737872	TTCCGCAGAAGCCGG[A/C]GCCACACCATGGCCG	84900
rs763321798	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845634	TACTCCAGGGTGTGA[A/G]GATGGGGCTGGACGG	84900
rs763333254	snp	A/G	7.25839e-05	0.00602384	intron-variant	RNFT2	GRCh38.p7	12:116849310	CTGATTGCTGTCCCC[A/G]CAGCACGTGTTCTGT	84900
rs763374541	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116834555	TAAGCAGTCACTCCC[C/G]ATTCTTCCAACCTCC	84900
rs763375346	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803388	TTATAAAATATTTCA[A/G]CTATACAGAAAATAA	84900
rs763428359	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833046	GCTTGAGTAGCCTCC[A/G]AGTAGCTGGGATTAC	84900
rs763455596	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116777740	TCTCATCAAATCCTG[-/C]CAATAACACCATGAG	84900
rs763470051	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761844	TGATCTCAGCCTCAG[A/G]TGCCGCCTCTGGAAA	84900
rs763472982	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116802555	GTTAGTGTAAAGATG[A/G]GGGCAGACATTGGGA	84900
rs763496780	in-del	-/GGAGGAGA			intron-variant	RNFT2	GRCh38.p7	12:116789925	GTAGATGGATGGATG[-/GGAGGAGA]GTGGATGGATGGATG	84900
rs763512935	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116846093	CACTGTCTACAATTA[A/G]GCACCCACTGTACAC	84900
rs763563108	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773115	TACAGGTATGAGCCA[C/T]CACGCCCGGCCAATT	84900
rs763571043	snp	C/T	0.000263913	0.0114842	intron-variant	RNFT2	GRCh38.p7	12:116836049	GCTTCAGGTGGTCCC[C/T]ACCAGGGTCCTGAGA	84900
rs763575550	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116750447	GATGTGGGATTCTGA[A/G]TCAGACCTGGGTTCA	84900
rs763588242	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829129	TGGGAGACATGAGGG[A/G]GGCATGGGGCAGCTG	84900
rs763608052	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823553	GCTGGGCGCCGTGGC[A/G]CATACCTATAATCCC	84900
rs763684205	snp	A/G	0.000129946	0.00805954	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750040	CAGATGCCCGCGTCC[A/G]GGGAGGAAGGAGGGG	84900
rs763715534	snp	A/G	1.8284e-05	0.00302352	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737861	GCACCCACCTCTTCC[A/G]CAGAAGCCGGCGCCA	84900
rs763723292	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116764849	ATGAGCTGAGATTGC[A/G]CCACTACACTCCAGC	84900
rs763753402	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116774309	CCTTTTATGTTATGT[A/G]TGTTTTACCACAATT	84900
rs763755624	snp	A/G	1.70766e-05	0.00292199	missense, intron-variant	RNFT2	GRCh38.p7	12:116849378	CCTGCCCGCTCTGCC[A/G]CTCGGTCGCCGTGGA	84900
rs763790042	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116794737	GAATTACTCTTAGCC[C/T]AAGATCCCAGAGCTA	84900
rs763821047	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116805193	ATCACTTCCTCTATC[A/G]CCCACTGCTTGGTGG	84900
rs763821246	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116827968	GACTGGTTGTTGAGA[C/T]TGGCCTGCAAGGAAG	84900
rs763907403	snp	C/T	0.000288122	0.0119991	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750111	CCACCATTTCCACCA[C/T]GGCGGCCACCGCGGG	84900
rs763998311	snp	A/C	4.69473e-05	0.00484473	missense, intron-variant	RNFT2	GRCh38.p7	12:116849422	TGGAAGGACGGCGCC[A/C]CGTCCGCACACTTCC	84900
rs764000557	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815106	ATAAATGATGTAGCC[A/G]GTCCTAGTAGTAGTA	84900
rs764046283	in-del	-/AAG	0.000144707	0.00850486	intron-variant	RNFT2	GRCh38.p7	12:116851753	CTGTCTAAAAAAAAA[-/AAG]AAAGAAAGAAGGGAG	84900
rs764065101	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116798022	AGCTCTCAACTTGGC[C/T]CCATATCTGAGCCCC	84900
rs764076990	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776145	TAGAGTAATTTAGAA[A/G]TGATTGGACTTGATG	84900
rs764110610	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757190	CCTGTTTCGTTTCTT[A/G]GTGAGGTCATTGGAT	84900
rs764144325	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810566	AGCAGGGAGACTCAC[A/G]TTCTTGGCTCCGAGA	84900
rs764148233	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116759236	TCTTTAAGCTATCTA[C/T]TTCCTTGAATATTTC	84900
rs764155069	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831018	CTCACACTCCTTGGT[C/T]TTCCCTTTGTCTTTC	84900
rs764190872	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116831534	CATTGTGTTTTTTAC[-/T]TTTTTTTTTTTTAGT	84900
rs764208769	in-del	-/CTC			intron-variant	RNFT2	GRCh38.p7	12:116832764	GCTTATCCTGTTCAT[-/CTC]CTTTAATCCTCAAAG	84900
rs764211506	snp	C/G	1.64846e-05	0.0028709	intron-variant	RNFT2	GRCh38.p7	12:116779191	CTCTCAATCCTCCCC[C/G]CAGCCTCATATTCCT	84900
rs764215148	snp	G/T	6.66778e-05	0.0057736	intron-variant	RNFT2	GRCh38.p7	12:116740539	GACACGTCTCCAAGA[G/T]AATTTGCATCTTTAT	84900
rs764307680	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116817672	GAAAAGCACCACAGG[G/T]ACTTCACTGTAAGTA	84900
rs764319273	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116760749	CTGTGGGTCCTCTCG[A/G]GATTGCTGGTTTGTC	84900
rs764353450	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116766261	TACTCCAGCCTAGGG[-/A]ACAGAAAAAAAAATT	84900
rs764376202	snp	A/G	4.95225e-05	0.00497582	intron-variant	RNFT2	GRCh38.p7	12:116836061	CCCCACCAGGGTCCT[A/G]AGAATCAGGAACTGG	84900
rs764387857	snp	A/G	3.11978e-05	0.00394942	intron-variant	RNFT2	GRCh38.p7	12:116750317	AGCTCGGTGAGTTCT[A/G]GGGGCATGGGTGTCC	84900
rs764391551	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746606	TTAGGGGAGACATCC[A/G]GTGAAGGTGATAGCC	84900
rs764402282	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116799766	CGTGTCTACTAAAAA[C/T]ATGTACCTGTCCCTT	84900
rs764403558	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116790269	ATGTGTTAAGCAATG[C/T]CATTTGTTCAAGAAA	84900
rs764439039	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116806130	TCATGCCTGTAATTT[C/G]AGCACTTTGGGAGGC	84900
rs764499067	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771069	GTTATGGCAGAGACC[A/G]TATAGCTTACAAAGC	84900
rs764519279	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116827931	TTTGGTTCCTGGGGC[C/T]GTGCTCTTGACCACC	84900
rs764519550	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783359	CTAGGGGGATGCTTC[C/T]GGTTGGCCTCCTCCT	84900
rs764519799	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116843691	CCACAGCCGTGAACT[A/C]CTCAGCTGGGCCCTG	84900
rs764570391	snp	C/T	0.00011536	0.00759387	intron-variant	RNFT2	GRCh38.p7	12:116835953	CACCACCCTGCTCTC[C/T]TTTCAGTCCTTCGAC	84900
rs764612654	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116801436	CGTCGAAAGAGCACA[-/T]TACTATACCCTAAAA	84900
rs764627135	in-del	-/TC			intron-variant	RNFT2	GRCh38.p7	12:116756607	ATTTTTGTTTTTAAT[-/TC]TGTTTACGTGGTGTA	84900
rs764650130	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116822137	ACCCTGCCTGGCCAA[A/C]CTCCTTCAACCAGAG	84900
rs764690298	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739871	GGCTTCCCCAATCAG[A/G]ACTCTTAGTTTGACA	84900
rs764705929	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739781	CATCAGGAAGAACCC[A/G]TAGGCTATGGACAGA	84900
rs764723083	in-del	-/AAC			intron-variant	RNFT2	GRCh38.p7	12:116816836	ATAAAAACAAAAAAT[-/AAC]AACAAATACTCGTGT	84900
rs764750540	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116740598	AGGAAGTTTTGGTTT[C/G]ACCACTCCACCCCTC	84900
rs764753883	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116823464	CGAAGTGTGTGGATC[G/T]CTTGAGGTCAGGAGT	84900
rs764774922	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116746335	CAGTGGGGTCGGGGC[-/A]ACCTGTCTTTTGCAA	84900
rs764779974	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116752116	ACACTTTGTGAGGCC[A/G]AGGCAGGAGGATTGC	84900
rs764785579	snp	C/T	0.000128386	0.00801103	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750121	CACCATGGCGGCCAC[C/T]GCGGGGGCTCCCTGC	84900
rs764785746	snp	C/T	1.64914e-05	0.00287149	intron-variant	RNFT2	GRCh38.p7	12:116835933	ATCCTTGGGTACATT[C/T]CAGCCACCACCCTGC	84900
rs764797954	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116783324	CCCTACACTGGCTTC[A/G]TGTTCTTGGGCTGGC	84900
rs764839794	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753242	TGCAGCCTCCCCATC[C/T]TGGGTTCAAGCAGTT	84900
rs764850638	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766544	GGATTTGAATGTGTG[C/T]CATGCTGCTCTGGAG	84900
rs764851295	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116796740	CCTTCTCCCAATCAG[A/T]CATCTGTCTATGCTG	84900
rs764857827	snp	A/G	0.000157307	0.00886728	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836202	GGAGTCCGAGCCACC[A/G]GGCAGCAGTGCACAG	84900
rs764873600	snp	C/G	3.5584e-05	0.00421791	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750172	CACCGGGGGCACTCG[C/G]AGGAGGGAGGCGACG	84900
rs764878579	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116837425	TTCCAGGTTGGGAAG[G/T]GTTTTTGGAGGAGGC	84900
rs764920635	in-del	-/TGGATGGG/TGGG			intron-variant	RNFT2	GRCh38.p7	12:116789972	GGGTGGATGGATGGA[-/TGGATGGG/TGGG]TGGATGGATGGATGG	84900
rs764941359	in-del	-/AAAC			intron-variant	RNFT2	GRCh38.p7	12:116764895	GAAAGTCCGTCTCAA[-/AAAC]AAACAAACAAAACAG	84900
rs764950950	snp	A/G	0.00035317	0.0132838	intron-variant	RNFT2	GRCh38.p7	12:116851721	ACTCCAACCTGGGTG[A/G]CAGAGTGAGTGAGAC	84900
rs764972989	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116817173	ACGCACTACCATGGC[C/T]GACTAATTTTTGTAT	84900
rs764978773	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835633	AGTGCTAGATGGAGA[A/G]GGGTTATCAGGGTGG	84900
rs764979823	snp	A/G	1.73881e-05	0.00294852	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833930	CTGATCGTTCTCTAC[A/G]GCCTCTGCAAGGTGA	84900
rs764981904	in-del	-/TGGGTGGA			intron-variant	RNFT2	GRCh38.p7	12:116839422	GATGGGATGGGTGGG[-/TGGGTGGA]TGGATGGATGGATGG	84900
rs765031642	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116776469	GCTCAGGGCCGCAAA[C/G]CTCTCCCTGTATTAT	84900
rs765048039	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757055	TGATTTAAGCGAGAA[A/G]GGTTGTATTTTTCCA	84900
rs765067096	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116772648	TTGGAAAACCCATTT[-/A]AAAAAGGACCAAAAA	84900
rs765105008	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829073	TAGTCCAGGGTAAGA[C/T]GGAATATGCAAGAGT	84900
rs765110872	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116788545	CCTACAGCACCCTAT[A/G]CTTCCCCTATTCTGG	84900
rs765122346	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116808828	TTGAAATTCTTGCTC[C/T]CCGTCCTGTGCTCCC	84900
rs765171424	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832620	TATGTATTCAACTTT[A/G]TTAGACACTACAGAG	84900
rs765190485	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746246	TGCTCAAAAAAAAAC[A/G]AGAATCACTGAGGGG	84900
rs765193630	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116756137	GAGGATTGCATTGAA[C/T]TTGTAGATTGCTTTT	84900
rs765199695	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116839142	CTGTGTTTTTCCTAC[G/T]TAGCACTTATTCCAA	84900
rs765225633	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116828064	GTTTCATGGGGTAGC[C/T]GTGTCCTTACCTGTC	84900
rs765269578	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116799547	AATGCAATTGCACAT[C/T]TCTTAGTATGCAGTA	84900
rs765278262	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116744951	GGGTACCTGCCAGGG[C/T]TCTTGCTTTCTGAGC	84900
rs765352102	snp	A/C	3.30819e-05	0.00406692	intron-variant	RNFT2	GRCh38.p7	12:116836073	CCTGAGAATCAGGAA[A/C]TGGAAACAGCAGCGA	84900
rs765364553	snp	C/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737247	GAATGCGCACCTCTC[C/G]CCACCCTCGGACGCC	84900
rs765393299	snp	C/T			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853378	ATATCTTGAGAATAA[C/T]AAATGTGAGGGAATA	84900
rs765410491	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116738042	GCCCAGTCTGCTCCC[C/G]GCAGCCTTGGGCGCA	84900
rs765437909	snp	C/G	6.87451e-05	0.00586241	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749869	GCGCTCAGCTCCGAG[C/G]CGAGTGTGGATGAAG	84900
rs765470056	snp	C/T	3.2594e-05	0.00403682	intron-variant	RNFT2	GRCh38.p7	12:116741137	GAGGGCTCTAGGCTT[C/T]GGGTGGTGAGGGGCA	84900
rs765528685	snp	A/G/T	3.29599e-05	0.00405944	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116753998	GGCATTGCTGTGTGC[A/G/T]TCGGGATGGCCAGCA	84900
rs765552185	snp	A/G	8.31947e-05	0.00644906	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737772	GGGAAGGGGAGGAGG[A/G]GAAGGGCGGCCACTG	84900
rs765574211	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116761763	GGGTAGTTGAGCCCG[C/T]GCTCATTCCAGGTTC	84900
rs765582788	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116760913	AGACAGAGTCTTGCT[C/G]TGTTGTCCAGGCTGC	84900
rs765646640	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116801276	GAAAGCCAGTGAGAT[A/G]CTAATCATTAGCAAT	84900
rs765676348	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116831126	GCACTTTGGGAGCCT[C/G]AGGTAGGAGGATCCC	84900
rs765740601	in-del	-/AAAAATATA			intron-variant	RNFT2	GRCh38.p7	12:116806378	GTCTCAAAAAAAAAA[-/AAAAATATA]TATATATATATATAG	84900
rs765747398	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116823140	TTTGTGACCTAATAC[A/G]TTTCCTTCTTTGTGG	84900
rs765771080	snp	A/G	4.71798e-05	0.00485672	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836245	TCTGCGCCATCTGTC[A/G]GGCCGAGTTCCGAGA	84900
rs765800893	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116845000	ATAATCCCAGCACTT[G/T]GAGAGGCCAAGGTGG	84900
rs765831537	in-del	-/AAA			intron-variant	RNFT2	GRCh38.p7	12:116806371	TGAGACTGTCTCAAA[-/AAA]AAAAAAAAATATATA	84900
rs765935061	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814006	AGTAAGTGCTAGGCT[C/T]GATTTATCAATTAGT	84900
rs765947843	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773122	ATGAGCCACCACGCC[C/T]GGCCAATTTTTCATA	84900
rs765959069	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116740818	CTGAGTCTCATCGTC[C/T]TCCTCTGTGAAATGG	84900
rs766000465	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824974	CATTTAATTCTCACA[A/G]TTTTGCAGGTCAGGA	84900
rs766004930	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116784626	CTCATTGTTCTAGAT[C/T]TCAGAGTGTAGCACC	84900
rs766033845	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116755508	GTTGAACCCAGGTAC[C/G]TTTCTCTTCCGCTTC	84900
rs766062464	in-del	-/CG			intron-variant	RNFT2	GRCh38.p7	12:116771497	AAAAAAAAAAAAATA[-/CG]CGTATATGAGCAATT	84900
rs766074070	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831943	AGACCAGCCTGGGCA[A/G]CATGGTGAAATCCTG	84900
rs766075288	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116757930	GTGGAATACTGAAGT[-/C]CCCTACTATTACTAT	84900
rs766126305	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116783636	AAGCTCTGACCCCAG[A/G]AACCCAGGATGGGAA	84900
rs766134239	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116753464	CGGTGAGTTTTTTCA[A/G]TGTATGCTTTTATCA	84900
rs766163291	in-del	-/CT			intron-variant	RNFT2	GRCh38.p7	12:116764858	GATTGCGCCACTACA[-/CT]CCAGCCTGGGCAACA	84900
rs766204947	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116838942	TTGCTCTGTTGCTGT[C/G/T]AGCTAGGCCTGGAAA	84900
rs766246889	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116818491	GTATGTTGCTGGAGG[C/T]CTTCTGAGGAGTGGT	84900
rs766248528	in-del	-/C	1.9812e-05	0.00314732	intron-variant	RNFT2	GRCh38.p7	12:116833981	CCGGCCTAAGGAGGG[-/C]CCCCATTCACTAGTC	84900
rs766281347	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116807095	TGTGGCTGGGTGCCA[A/G]TGGCCCTAAGCAAAG	84900
rs766287783	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779226	CCCAACCTGGAGATG[C/T]TGGACTTCTTTGACC	84900
rs766306785	snp	A/G	5.36553e-05	0.00517926	missense, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836257	GTCAGGCCGAGTTCC[A/G]AGAGCCTCTGATTCT	84900
rs766309887	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778116	CCCTCTCTTCCTCCC[C/T]CTTTCTTTTCTTCCC	84900
rs766315739	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116829653	ACATGCCACGCATAC[A/G]ATGTAATCTTGGCTC	84900
rs766467388	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116831789	ATGAGTTTTGGCAAA[-/C]GTGCGCACCCATGTA	84900
rs766475084	snp	A/G	0.000100893	0.00710185	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749993	CCAGCCTGGTGCTGG[A/G]CTCCTCGGCTGGCGG	84900
rs766483340	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781156	AGCTGTGCAATCTTG[A/G]ATGAATTACTTAGCC	84900
rs766548145	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116841004	TTAAATGCTTCAAAC[A/C]TCCTTTCCCAGATTC	84900
rs766548841	in-del	-/CTC			intron-variant	RNFT2	GRCh38.p7	12:116824165	ACCCTCCCCGTCTCA[-/CTC]CTCCTACCCTCATCA	84900
rs766577691	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116837216	CAAATGTGTATTGGG[A/G]TCAAAGCATCCTATC	84900
rs766594516	in-del	-/TTGTTG			intron-variant	RNFT2	GRCh38.p7	12:116759620	GCCAAACTGCAGTGA[-/TTGTTG]TCTGTCTTCTGGGTC	84900
rs766670718	snp	A/G	1.89106e-05	0.00307489	upstream-variant-2KB, missense	RNFT2, C12orf49	GRCh38.p7	12:116737876	GCAGAAGCCGGCGCC[A/G]CACCATGGCCGCCAG	84900
rs766680762	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737339	AGGAAGGGAAGGAAG[A/G]AGGAAGAACGAAGTG	84900
rs766689378	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746130	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATA	84900
rs766691845	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116749049	CGACCTATTGTTATT[A/C]ATATTATTTGTATTA	84900
rs766694981	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810721	TTAAGCAAGGCAGCC[A/G]GGCTCCCTGAGGGGG	84900
rs766702108	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116800628	GACAGAGCAAGACTC[A/T]GTCTCAAAAAAAAAA	84900
rs766716752	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116750342	GTGTCCTAGCCATGG[A/G]CTTCACAGGCAGGCT	84900
rs766740722	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116769073	ACTTGTAAAAAATAA[A/C]AGTTGGCCGGGCGCA	84900
rs766749950	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820858	GAGTCTGGGGACAGC[C/T]TGCAGGTACTAAGTG	84900
rs766754982	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116821059	AGCAATTGGTGTGCC[A/G]TTCCTGGCCCCTGGT	84900
rs766792296	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116834566	TCCCCATTCTTCCAA[C/G]CTCCCCTTCCCCCAG	84900
rs766818056	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116743415	GGGACCATAGGCACG[C/T]ACCACCACGTTTGGC	84900
rs766844937	in-del	-/GGATGGAT			intron-variant	RNFT2	GRCh38.p7	12:116788956	TAAATGGGAGGAGAG[-/GGATGGAT]GGATGGATGGATGGA	84900
rs767006824	snp	G/T	1.64743e-05	0.00287	utr-variant-3-prime, missense	RNFT2	GRCh38.p7	12:116852679	GCACAAGAAATTGGA[G/T]CTGGAGAAGATTGAT	84900
rs767088638	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116803802	GATGAGACCTCAGTC[C/T]CCACTGGAACCTCAA	84900
rs767100739	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116806575	ACATAGTGAGACACC[G/T]TCTCTATAAAAAAAA	84900
rs767104150	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116846237	TTATAGAGCACTTAC[C/T]ATTTGCCAGTCATTA	84900
rs767137679	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116814974	CTCCTGACCTCAGGT[C/G]ACCCGCCTGCGTCGG	84900
rs767165322	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116743589	TTATATCTATTGAAA[C/T]CCAAGAGGGAACACA	84900
rs767168477	snp	C/G	1.64822e-05	0.00287068	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116753992	CCCACAGGCATTGCT[C/G]TGTGCATCGGGATGG	84900
rs767194375	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116762163	GCAGGTGGATCACTT[C/G]AGGTCAGGAGTTTGA	84900
rs767240872	snp	A/G	1.76201e-05	0.00296812	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750016	GCTGGCGGCGGGGAC[A/G]TGTTCATCCAGATGC	84900
rs767251234	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116742138	GAGGGCAGAAAGGAC[C/T]GAGGAAAAAGCATAG	84900
rs767260651	snp	A/G	2.12366e-05	0.0032585	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737768	AGAAGGGAAGGGGAG[A/G]AGGGGAAGGGCGGCC	84900
rs767309607	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748481	CTATTATTGCAAAAC[A/G]TATTTTAAATTTAAC	84900
rs767329070	snp	C/T	0.000212269	0.0103	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750099	CCGCCAGCCCCACCA[C/T]CATTTCCACCATGGC	84900
rs767344101	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116768098	CTTTGCACAGTTTGG[-/C]CTTTTTTTTTTTTTT	84900
rs767351088	snp	C/T	1.65094e-05	0.00287305	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833833	GCTGAGCCAGCTGTT[C/T]CGATCCCTTGTCCCC	84900
rs767373896	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116814858	TAAGTTTTCTATTTT[A/T]AGTACAGATGGTGTT	84900
rs767375893	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116795118	TTGCCTCTTTATGAA[A/T]ATGAAGGCCGGGCCC	84900
rs767389962	in-del	-/AGG			intron-variant	RNFT2	GRCh38.p7	12:116787254	CTACTTCTGAGGACC[-/AGG]AGATCATCTGCCAGA	84900
rs767396971	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825112	GCAATGGCAGGAATG[A/G]CCTTCTTAAGGTCCT	84900
rs767414993	in-del	-/TGGCCT			intron-variant	RNFT2	GRCh38.p7	12:116825636	TTGGTAGCTTGAAGC[-/TGGCCT]TGTGGGAACATTTAT	84900
rs767437355	snp	C/G/T	0.000124885	0.00790125	synonymous-codon, missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749895	TGAAGGTGGCGTCTT[C/G/T]GAGAGTCTGAAGGCA	84900
rs767464992	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116767745	CCACCACGCCCAGCG[A/C]ATTTTTGTATTTTTA	84900
rs767477849	in-del	-/AGAA			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737648	AAGGAAGGGAAGGGG[-/AGAA]AGAAAGGAAGGGAAG	84900
rs767490857	in-del	-/TA			downstream-variant-500B	RNFT2	GRCh38.p7	12:116853688	CAAGTGCAACTGTCT[-/TA]GATCAAAGGAGAAGA	84900
rs767502373	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116787692	ACACTCAGCCTGGGC[A/C]ATAGAGGGACATGTT	84900
rs767516380	snp	C/T	1.97416e-05	0.00314172	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737886	GCGCCACACCATGGC[C/T]GCCAGGTTCACCATC	84900
rs767524197	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736965	GGCCGACCCTCGCCA[C/T]CTATGTCTTGGTTTC	84900
rs767534719	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116759648	TCTGGGTCTAGCCAC[C/G]CAGCGAGTCTACCTG	84900
rs767536274	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	RNFT2, C12orf49	GRCh38.p7	12:116737998	GGCAGCCCCATCCCT[C/T]CAGGCAGGCGCCGGC	84900
rs767591860	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116843181	GTGCTTCGGGAGGCA[C/T]GACCAGGGGGCAGTT	84900
rs767636195	snp	A/G	0.000104685	0.00723404	missense, intron-variant	RNFT2	GRCh38.p7	12:116849416	CGCTGCTGGAAGGAC[A/G]GCGCCACGTCCGCAC	84900
rs767647691	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116833295	GAGCTAGGAAGGACA[C/T]GTATCTCCCCGCTTT	84900
rs767727808	snp	A/G	4.38395e-05	0.00468165	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766879	GAACACCCTCTATGT[A/G]CTTTATACATTCAGC	84900
rs767744275	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116745019	TGAGGATCATAGCCA[C/T]GGTGTTTGCTGTTGT	84900
rs767765518	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116758708	CCCTTCTAGCTTGTA[A/G]GGTTTCTGCTGAGAA	84900
rs767770129	in-del	-/TTCTC			intron-variant	RNFT2	GRCh38.p7	12:116800461	AACATGGTGAAACTT[-/TTCTC]TACTATAAATATAAA	84900
rs767799763	in-del	-/TA			intron-variant	RNFT2	GRCh38.p7	12:116837990	GTATGTATATGTGTG[-/TA]TATATTTATACACAC	84900
rs767808752	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116818274	GCTGCAGTGAGCTGA[A/G]ATCGCACCACTGCAC	84900
rs767841244	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842200	TGTGGCCAGTAGATA[C/T]CCTGAGTTCTGGAAG	84900
rs767858590	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116743197	GCCCTGTGATTAATA[A/G]ATACCAGGTAGAATC	84900
rs767861531	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116851743	AGTGAGACTCTGTCT[-/A]AAAAAAAAAAAGAAA	84900
rs767866557	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116846108	GGCACCCACTGTACA[C/T]CATGCTAGGAATGAA	84900
rs767883383	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781297	TGACCTGCGCGAACT[A/G]TATCAATGGGCTCCT	84900
rs767890073	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116811656	GCTGGGATTACAGGC[A/G]TGAGCCAACGCACCC	84900
rs767989157	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116766136	ATTTTTTTTTAATTA[A/G]CCAGGTATAGTGACA	84900
rs767996793	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116835757	ATTCTGGCCTAGGTA[G/T]CAGGGGAAACTCTTG	84900
rs768008184	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116780447	CTACTGCCGCAGCTG[A/T]TCTGATGGGAGGCGG	84900
rs768025928	in-del	-/AGAAGTCACC			intron-variant	RNFT2	GRCh38.p7	12:116775330	CTTACTGAAGTCACC[-/AGAAGTCACC]AGTCTAGACGGTGCT	84900
rs768033580	snp	A/G	0.000123047	0.00784271	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116740512	CATGTGGCTCTTCAC[A/G]GTGAATCAGGTGACA	84900
rs768042315	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116829364	TTCCCAAAAGTTCCA[C/G]AGGGAAACCAGCATT	84900
rs768151661	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116750524	CTCTGAGCCTCAGTT[G/T]CCTCATCTGTCTAGT	84900
rs768157271	snp	C/T	2.41135e-05	0.0034722	intron-variant	RNFT2	GRCh38.p7	12:116741025	TGGCTCACCCATGTG[C/T]TGGGTTTTAGGTGTT	84900
rs768238825	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116816840	AAAACAAAAAATAAC[A/G]AATACTCGTGTACCC	84900
rs768243937	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116772856	TATTTTGAGACAGAG[A/T]CTTGCTCTGTCGCCC	84900
rs768273667	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116788776	GGATATATAGGTAGG[G/T]AGATAGATGAATTAG	84900
rs768286602	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817982	ACTTCAAGTTTCAAC[A/G]AGCACTAGAGACAAA	84900
rs768292012	in-del	-/CAT	1.64985e-05	0.0028721	intron-variant	RNFT2	GRCh38.p7	12:116753959	AGTCTAAGTGGGTGA[-/CAT]CAGGCCCTTCTCTGT	84900
rs768351635	snp	A/T	7.17849e-05	0.0059906	intron-variant	RNFT2	GRCh38.p7	12:116766946	AACCCCCACGGTGGG[A/T]GAGTGGGGCACTTGG	84900
rs768356270	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116746018	AAGGCGGGTGGATCA[C/T]TTGAGCTCCGGAGTT	84900
rs768400219	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116787307	CTAGGCCATTCCTAA[C/T]CTGCAATTTTCCAGC	84900
rs768413122	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116817090	CGATCGCAGCTCACC[A/G]CAACCTCCACCTTCT	84900
rs768451499	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116799417	CAAAATCCCTTTTAT[C/T]GTGTAGCCTGTAATA	84900
rs768459241	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781895	CAGCCTGGGCTACAC[A/G]GTGAAACCCCGTCTC	84900
rs768475435	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811551	TGGCTAATTTTTGTA[C/T]TTTTAGTAGAGACGA	84900
rs768520139	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116842872	AGCCACTGTGCCCGG[A/C]GTGTTTATACTTTAT	84900
rs768524763	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116821585	ATACCCTGGGGCTTT[C/T]GGGAGCCAACAGGCA	84900
rs768611278	snp	C/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739375	ACTCTGTGCCAAACA[C/G]TGTCCTGGATGCTGA	84900
rs768641645	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116770440	AGGTCACCTAAGGAT[A/G]TGTTTCTCAGAACAT	84900
rs768661034	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116756307	GGTATATTCCTAAGG[-/T]TTTTTTTTGTTTTTT	84900
rs768686671	snp	G/T	1.64972e-05	0.00287199	intron-variant	RNFT2	GRCh38.p7	12:116835925	CACGAGTGATCCTTG[G/T]GTACATTTCAGCCAC	84900
rs768760497	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116761539	CACCATCCTCCTGCA[A/T]GTCCTCTGTGTCTGC	84900
rs768763214	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116748585	AAGGCCCCTAGAACA[C/G]GTGGAGCTGGAGTTT	84900
rs768793575	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773719	AGGGTGATGGGAATC[A/G]CATCTCTACATCAGA	84900
rs768802130	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832474	TTCTTCCATTGATGG[A/G]CGTCTGGGCTGCTTC	84900
rs768813086	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813545	GTGCTTCCATAGCCC[C/T]GAGGCCACTTCTGTT	84900
rs768848887	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116756311	TATTCCTAAGGTTTT[A/T]TTTTGTTTTTTGTTT	84900
rs768868109	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116809599	CGATTCAGACATCCC[A/G]GAGGTCTCTCTGGTT	84900
rs768880616	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116846732	TCCAGATTTACTGAT[A/C]ATTAACATTTTACAT	84900
rs768885535	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116772921	GTAACCTCCGTCTCC[G/T]GGGTTCAAGCAATTC	84900
rs768889201	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779291	GAAGTACATCACCAT[C/T]GCCCTCAAGTGCCTC	84900
rs768922492	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116814541	AAAGGCCCTGAGGTG[C/G]AAACGTGCTTGGCAA	84900
rs768997890	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116818868	TGCGGGGGCACGCCG[-/C]CAAGTGGGACCGTTA	84900
rs769030718	snp	A/C/T	0.000178902	0.0094564	synonymous-codon, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836237	TGGTGACATCTGCGC[A/C/T]ATCTGTCAGGCCGAG	84900
rs769095913	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838442	ACTGGGTCAGAAGGC[A/G]CACAGTTTTGACAGT	84900
rs769117784	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741794	GCTGGGACTACAGGC[A/G]TGTGCCACCATACCT	84900
rs769122794	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116783105	ATCTTTCCTCCTCCT[A/G]CTGCTGCTACCACCC	84900
rs769132565	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116800854	AAAATAAAATAAAAT[-/AA]AATAAAAACCATTTA	84900
rs769135653	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116755123	TTATAGTTTTAGGTC[C/G]TAGGTTGAAATCCTT	84900
rs769174037	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116796699	CTTCGCTCCTGGAGG[A/T]CATACCTTCCCCTCT	84900
rs769213526	in-del	-/TGTGCCA			intron-variant	RNFT2	GRCh38.p7	12:116814471	AAGGAAGCAAGGGAG[-/TGTGCCA]TGTGGATATGTGGGG	84900
rs769238760	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768347	CTCAGGTGATCCGCC[A/G]GCCTTGGCCTCCCAA	84900
rs769256667	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116808731	CTATTGAACCAAATG[A/G]TACTGTTTGTTTTTA	84900
rs769264818	snp	C/G	7.71337e-05	0.00620974	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749856	AAACCGCAGCCAGGC[C/G]CTCAGCTCCGAGGCG	84900
rs769267063	snp	G/T	1.69991e-05	0.00291535	intron-variant	RNFT2	GRCh38.p7	12:116779395	CAGTCACATGGATCA[G/T]GCAGAGGATTCAGGG	84900
rs769274753	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736762	AAGATTTCCCCACCC[A/G]TGCTCCTTGCTGTTT	84900
rs769295475	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753030	AAGAAAATTCAATTC[C/T]GTTCTGCCATCTGCC	84900
rs769315898	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116818971	AAAAGGCTGTCAAAG[A/G]GCTCATTCACATCAT	84900
rs769316912	snp	C/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736749	TAATGCTTTGGGTAA[C/G]ATTTCCCCACCCGTG	84900
rs769414644	snp	C/T	2.44382e-05	0.0034955	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116741089	GGATAACATTCCACC[C/T]GAAAGGTAGGCATCC	84900
rs769414783	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778755	CTTGGGAAGCTGAGG[C/T]GGGAAAATCACTTGA	84900
rs769447000	snp	C/T	4.94336e-05	0.00497135	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836019	GAAGCTTCTCTGTAC[C/T]TCTCAGGTGAGTTGG	84900
rs769474028	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831706	AGTGTTGTTTGTTTG[A/G]TTTTATCAGCTTTAT	84900
rs769477013	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116823905	CCATTAGCCCCATTT[-/T]ACTAGCGAGGAAACT	84900
rs769491256	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116788867	ATGGGAGGAGAGTGG[A/C]TGGATGAATGGGTAG	84900
rs769502629	snp	A/G	0.000195484	0.00988453	intron-variant	RNFT2	GRCh38.p7	12:116748727	GACTGCAGAGCCAGC[A/G]GTCCTTGGGATCCCG	84900
rs769536116	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116818231	GTGGGGCTGAGAGGG[G/T]AGGCTCGCTTGAGCC	84900
rs769641368	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116771900	CCACAAATCTGCCAA[A/C]GTAAATGAAGCAGGC	84900
rs769646289	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116801701	GTTAGAATCTAACCA[A/C]AGTCAGGATCGAACA	84900
rs769657266	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116747118	CTGGAGTGCAGTGGC[A/G]TGATCTTAACTCACT	84900
rs769688626	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116747679	TGTGTGCCCTGGGTT[G/T]TGGGGTCCAGAGGAT	84900
rs769689859	in-del	-/TGG			intron-variant	RNFT2	GRCh38.p7	12:116788979	GGATGGATGGATGGA[-/TGG]ATGGGTAGATAAATG	84900
rs769733957	in-del	-/TTTTT			intron-variant	RNFT2	GRCh38.p7	12:116742265	TACCGAGGTGGTTTC[-/TTTTT]TTTTTTTTTTTTTTT	84900
rs769777775	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760309	GGGTTTAGTTCGTGC[C/T]GCCGCTGTGGAGTCT	84900
rs769793201	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842980	TGCTTTCTCGGCTCA[C/T]GCTGAACACCAAGTG	84900
rs769793828	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800673	GCAAAAAATTAGCTG[A/G]CACTGTGGTGCGTGC	84900
rs769820551	snp	C/T	3.87845e-05	0.00440349	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836198	CTATGGAGTCCGAGC[C/T]ACCGGGCAGCAGTGC	84900
rs769820698	snp	A/C	6.26586e-05	0.00559691	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750268	GGACTCCCCTTCATC[A/C]TGATCCTCCTGGCCA	84900
rs769840463	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751396	TAATTGGCCTCTAGT[A/G]TACTGTTTTCTGTTT	84900
rs769880355	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116780825	TCCAGGTCGGCACCA[C/T]GCACTTGACACTGGA	84900
rs769896467	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766649	CTCCGTGACCACCGC[C/T]TGGGTATCAGTGGAA	84900
rs769900128	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116812271	TGGCACATAGCAGCC[C/T]GACATAAATACACAC	84900
rs769906259	snp	A/G	1.65029e-05	0.00287248	intron-variant	RNFT2	GRCh38.p7	12:116753953	CTGATGAGTCTAAGT[A/G]GGTGACATCAGGCCC	84900
rs769931520	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116793952	CTCTTGACTCACAGG[A/G]AATGTACCACTGTGG	84900
rs769951828	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116820627	TTTCTTTCTCTTTCT[C/G]CCACATCTTACTTTA	84900
rs769959799	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116764420	ACCAGCTTCACTGAC[C/T]CTTCTATAGCATCGT	84900
rs769972002	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116839410	GATGGATGGATGGAT[-/G]GGATGGGTGGGTGGG	84900
rs769977065	snp	A/T	1.65067e-05	0.00287282	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852759	TGGAATTCTGATTCC[A/T]AACTCTTTATTACTT	84900
rs769989838	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116773994	AATTCTGACACATGC[C/T]GCAACATGGATGAAA	84900
rs770004036	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116752479	GAGAAGAGTACCAAA[A/C]AGGATTATGGGGCTA	84900
rs770005133	snp	A/G	1.76742e-05	0.00297268	upstream-variant-2KB, missense, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737812	AAGGTGCTGCTGAGG[A/G]AGTAGACGAGCGACA	84900
rs770022220	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116744169	AGGTGGAGGCTGCAA[C/T]GAGCAGAGATCATGC	84900
rs770028881	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116835343	CTCAAAAATAGTATC[C/T]GTGTTAAATTGCACA	84900
rs770084984	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116834161	TCTCACTCTGTCTCC[C/T]AGGCTGGAGTTCGGT	84900
rs770094031	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803309	CCTCTTGTTCCAGTT[A/G]TCATTAGTTGCCTGT	84900
rs770096066	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815704	GCACAAAATTCCTTT[C/T]GCCCTGTAAGGTACC	84900
rs770115475	snp	G/T	1.65266e-05	0.00287455	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833797	GTGGTTGCAGGGAAA[G/T]TTCTATCTGGTCATC	84900
rs770143150	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116805971	TCAGTGTTTGATTGC[A/G]TAACTAAATACTACA	84900
rs770148973	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814748	CAGTGGTGCAATCTC[A/G]GCTGGCTGCAACCTC	84900
rs770176100	snp	C/T	0.000257632	0.0113468	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750085	GGCGCCTACCACCAC[C/T]GCCAGCCCCACCACC	84900
rs770206623	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741889	CTCCTGGGCTCAAGC[A/G]ATCTTCCTACCTTGA	84900
rs770214964	snp	A/G			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852885	AGTGAATACCCCAAT[A/G]GTTTCTCCAATTATG	84900
rs770229793	snp	C/T	0.000658111	0.0181279	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849388	CTGCCGCTCGGTCGC[C/T]GTGGACACCCTGCGC	84900
rs770243719	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116824913	AGCTGAGTAGCCTTA[G/T]ATGGTACTTTAGTTT	84900
rs770285499	in-del	-/TCACCAGAAG			intron-variant	RNFT2	GRCh38.p7	12:116775325	TTGTCCTTACTGAAG[-/TCACCAGAAG]TCACCAGTCTAGACG	84900
rs770321976	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116825762	GTATGTGTGTATGTA[C/T]GTGTGTATTCAACCC	84900
rs770338103	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116756589	TATTGAAATGATCAT[G/T]TGATTTTTGTTTTTA	84900
rs770340748	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786008	AGTGAGCTGAGACCG[C/T]GCCACTGCACTCCAG	84900
rs770368401	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116825868	ATGTGACCTTAGAAT[C/G]CCAAATCCCACGCCT	84900
rs770375146	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116839865	GTCACTCCCACTCCA[C/T]CCACTACCCCCTGAG	84900
rs770394996	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838095	TTAACTTAAAACTCT[A/G]TCTTAGAGATTGCTC	84900
rs770486009	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116768487	ACAGTGGTCCCATAA[C/G]GTTATAATGGAGCTA	84900
rs770521628	in-del	-/CG			intron-variant	RNFT2	GRCh38.p7	12:116817955	TAAACTATATCAACA[-/CG]CAAATATAGAACTTC	84900
rs770561660	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791606	TGAGCCACCATGCCC[A/G]GCTTTCATTCCTTCT	84900
rs770638784	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768453	ATGATGTTTCTGTCA[A/G]CGATGGACCATATAG	84900
rs770638966	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116840243	TACAAGTTCTTCATA[C/T]TTGACCTTATCTGTC	84900
rs770663238	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809188	TTAGAGCTGAGTTTG[C/T]TCATTCATTCATTCA	84900
rs770691107	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748394	AGGCCCTTGCTTGGA[A/G]CTAGAGAAAGCAATA	84900
rs770709471	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116819724	CCTGGCTCGCCCTTC[C/T]CTTGCCTTTTTTCCT	84900
rs770731716	snp	A/G	1.65102e-05	0.00287312	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833823	TCATCGAGGAGCTGA[A/G]CCAGCTGTTCCGATC	84900
rs770732670	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800669	AAATGCAAAAAATTA[A/G]CTGGCACTGTGGTGC	84900
rs770739944	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116819357	TACCGGCGCGGGACG[C/T]CCGGAGGCCAGACCC	84900
rs770792955	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116832008	TGGTGGTGTGTACCC[A/G/T]TGATCCCATTTACTT	84900
rs770803600	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761481	TCCACCTTCATGCTT[A/G]TGGCCATTCCTCTTA	84900
rs770823068	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736898	GTCCTTTTGAGTCAC[C/T]CAGGAGGACACAGAG	84900
rs770836632	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845674	CATCATAGAGGGTAA[C/T]GGGTGCCATAGTGGG	84900
rs770852701	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116782989	AGACTTCCCTCATGG[C/T]GAGAACAGAGTTTAT	84900
rs770904770	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116792091	CAGAGTCTCTGTTGC[C/T]CAAGCTGGAGTTCAG	84900
rs770919443	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116830981	TTACATTATTTGTCA[C/T]GTCTCCTTAATTCTC	84900
rs770937021	in-del	-/TG			intron-variant	RNFT2	GRCh38.p7	12:116840924	AGGGGTATGTGTCTG[-/TG]TGTGTGTGTGTGTGT	84900
rs770978159	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116770796	ACTCCTTGCCTCAAG[A/T]GATCCACCCACCTCA	84900
rs771001546	snp	G/T	3.33951e-05	0.00408613	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750147	CCTGCTGCAGCACGT[G/T]GGTGGGGACCACCGG	84900
rs771016543	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116784888	TCCCTGCCAGCGGAG[C/T]AGGACTCTAAAAGAA	84900
rs771058587	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739540	TATTACGGGGAGTCA[A/G]GAGAATGAGAAGAGA	84900
rs771109793	snp	C/T	5.03529e-05	0.00501736	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833904	CCAACAGCTACTTCC[C/T]GGGCGGGGTCCTGAT	84900
rs771114118	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116795386	GCACTCCAGCCTGGG[C/T]GGCAGAGTGAGACTC	84900
rs771124890	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116836902	GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGCA	84900
rs771173770	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116848911	TGCAACCTCTGCCTC[C/T]GGGTTCAAACGATTC	84900
rs771236661	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116794115	ATAAAAAACTAAAAA[C/T]GTATCCAAGCATAGT	84900
rs771241845	snp	A/C	0.000117158	0.00765279	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750092	ACCACCACCGCCAGC[A/C]CCACCACCATTTCCA	84900
rs771271481	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116825655	CTTGTGGGAACATTT[A/T]TACCACAGAAATTGG	84900
rs771334993	snp	C/T	6.99227e-05	0.0059124	missense, intron-variant	RNFT2	GRCh38.p7	12:116849399	TCGCCGTGGACACCC[C/T]GCGCTGCTGGAAGGA	84900
rs771354229	snp	C/T	3.31433e-05	0.0040707	intron-variant	RNFT2	GRCh38.p7	12:116779158	GCTGAGGCCTGGCCC[C/T]AAGGGAACCTTCTGA	84900
rs771362167	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116770690	GACTCCCAAGTAGCT[-/G]GGGACTTCAGGCGCA	84900
rs771366276	in-del	-/G	6.26429e-05	0.00559621	frameshift-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750123	CATGGCGGCCACCGC[-/G]GGGGGCTCCCTGCTG	84900
rs771387714	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116851007	CCCAAATACTTCATG[C/T]GCAGCAGGCAAAGCA	84900
rs771433716	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116841630	GCACACACCTGTAGT[-/C]CCAGCTACTCGGGAG	84900
rs771450017	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786988	TAAGGACACATGTAA[C/T]GGTATTTTGGGCCCA	84900
rs771454256	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116815843	TGATTGATATGACTT[C/T]GGCAAAGTCACCCTC	84900
rs771509154	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116826986	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	84900
rs771543074	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116745693	AAAAAGAATTCTGTG[A/G]TCAAATAAGTTTGGG	84900
rs771543719	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116759069	TCTTATTCCCTTTTC[A/T]TTGTCTTTGTTGGAT	84900
rs771543997	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116788285	ATCCCTATGTGGTAG[A/G]TGCTGTTCTTATCCC	84900
rs771544638	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774121	AGACAGAAAGAATGG[C/T]GGTTGCCAGGGACTG	84900
rs771617567	snp	C/T	4.19789e-05	0.00458123	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766855	GTGGATCCTGGCCTT[C/T]CTGGCGGGGAACACC	84900
rs771630974	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116744541	CAGCCAGGAAGTAGC[A/G]GGGCTGAGATTTGGG	84900
rs771657446	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116799932	AGTTGTTTGGGTCAC[-/A]GGGGTGAATCTCATG	84900
rs771680424	snp	C/T	4.94841e-05	0.00497389	intron-variant	RNFT2	GRCh38.p7	12:116754085	TTTCCGACCTAGTCT[C/T]CTGTGGCTGCTGCAA	84900
rs771736773	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828743	TAAAAGGCAGGAAGG[A/G]AGGGAAGGAAGAAAG	84900
rs771759539	in-del	-/CATCTCTTAGTATGCAGTATTTATAAGTTAGCTGTG			intron-variant	RNFT2	GRCh38.p7	12:116799544	GAAAATGCAATTGCA[lengthTooLong]TTTTTTTTTAACAGC	84900
rs771763070	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116757898	TTTCTGTCTTGATGA[C/T]CTGTCTAGTGCTGCC	84900
rs771794940	snp	C/T	0.000115556	0.00760032	intron-variant	RNFT2	GRCh38.p7	12:116835912	ATTGTGCAGGGGTCA[C/T]GAGTGATCCTTGGGT	84900
rs771817602	snp	A/G			upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738104	CCGCTCCGCAGCGAC[A/G]AGGGCTAGTCGCGCA	84900
rs771821105	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116798614	GTCTCTGTCACCCAG[G/T]TTGGAGTGCAGTGGC	84900
rs771825822	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116768640	CATGCAATTATGTAC[A/G]GTACCTAATGCTTGA	84900
rs771835306	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116795234	AACATGGCAAAACCC[-/T]ATCTCTACCATAAAA	84900
rs771840416	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116769493	GACAGTGATATTGAT[A/G]ATTCTGACCCCACGT	84900
rs771842419	snp	A/G	1.68627e-05	0.00290363	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833910	GCTACTTCCTGGGCG[A/G]GGTCCTGATCGTTCT	84900
rs771865218	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739227	TCACGGAGGCTAAAC[C/T]TTTTCATGGGAAGTA	84900
rs771895891	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116819219	GGTGAAATGTCCAAA[G/T]AAGAGAGCGGGGAGT	84900
rs771946077	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116834003	TCACTAGTCAGGCCT[C/T]AGGGGGCTCCTGGGC	84900
rs771991304	in-del	-/GATG			intron-variant	RNFT2	GRCh38.p7	12:116789444	GATGGATGGTAGATG[-/GATG]GATGGATGGATGGAT	84900
rs771997715	snp	C/T	0.00177515	0.0297392	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737940	GGCCGGGGCGCGGAA[C/T]GCGGCAGGCCCGGGT	84900
rs772000489	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766361	GCCCCTTGAGGTTTC[C/T]TAACCTCTCTGTGCT	84900
rs772020919	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739051	ATTTTTAATCAGTGG[C/T]CCTAGTGACACCATT	84900
rs772029561	in-del	-/GATG			intron-variant	RNFT2	GRCh38.p7	12:116789615	GGTGGATGGATGGTA[-/GATG]GATGGATGGGAGGAG	84900
rs772055625	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116780744	GAAGTCCTAAGATGC[C/G]TCCCATTGACCCTCC	84900
rs772080709	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772796	ACCAGCATATCACTT[C/T]AATGCACAAGAAATG	84900
rs772112829	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116793704	TTCCTGGATGTTTCC[A/G]TGGCTGTCTCCTTCC	84900
rs772112873	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116780238	GTGTGACTTAACATG[A/G]TGGTCCCCAACCTTT	84900
rs772167466	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116844844	AAGTACCTCTTTTGT[A/C]CAGGGTAGCATAGTT	84900
rs772220172	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116822943	CAGAGATTGCAGTGA[A/G]CCAAGATTGAGCCAC	84900
rs772251219	in-del	-/C	5.02567e-05	0.00501257	intron-variant	RNFT2	GRCh38.p7	12:116779377	GCGGCCACAAGGTAG[-/C]CCCAGTCACATGGAT	84900
rs772271751	snp	C/G			utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852404	TTGGCATCCCTGGCT[C/G]TCTCCTGGTACCCAG	84900
rs772279709	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116796476	GAGGTTCCAGTAGGG[C/T]GAGATTCCATAGGCT	84900
rs772295715	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116793024	TGCCAATGCCAATTC[C/T]CACGTGCCTTGCAAC	84900
rs772310948	snp	A/G	3.46374e-05	0.00416143	intron-variant	RNFT2	GRCh38.p7	12:116849489	GGACGCCAAGGGTCA[A/G]CATGCCCGGACCCAG	84900
rs772340702	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807608	GCACCATTCCCCACT[C/T]GCACTCCCCTGACCC	84900
rs772344172	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116745551	TAGGCATGAGCCACC[-/A]TGCCTGGCCTCACTA	84900
rs772408143	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116812625	CTGCAACCTCCACCT[C/G]CTGGGTTTAAACGGT	84900
rs772447891	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116837067	TCATTGTCATCTGTA[C/T]AATTATTATTACCAT	84900
rs772463462	in-del	-/TTTT			intron-variant	RNFT2	GRCh38.p7	12:116846902	CTAGCATGCCCAGGA[-/TTTT]TTTTTTTTTTTTTTT	84900
rs772595496	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116840106	CCAAAGAGAAGAGTA[A/G]GAGTGCATTTAGAGA	84900
rs772621523	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116848944	TTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	84900
rs772651708	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116777345	TTTTAGCCACTATTA[A/C]AAAGAACATCCCCCT	84900
rs772651811	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116756618	TAATTCTGTTTACGT[C/G]GTGTATCACATTTAT	84900
rs772675497	snp	A/C/T	0.000131918	0.00812054	intron-variant	RNFT2	GRCh38.p7	12:116779187	GACTCTCTCAATCCT[A/C/T]CCCCCAGCCTCATAT	84900
rs772695468	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116753200	CTGTTGCCCAGGCTG[G/T]AGTGCAGTGGTGTGA	84900
rs772775969	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116824948	TGTTGTTGTTGTTGA[C/T]TTGAAAAAACCATTT	84900
rs772781242	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116778938	CACAAAAAAAGGACT[A/C]AAACAAGGACCTTAA	84900
rs772794629	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116755921	GCTGAAAGGAAAAGA[A/T]ATGTCCTTATTTTTG	84900
rs772821287	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116756394	TTGGTCGCCGTTGGT[A/G]TATAAAAGAGCTACT	84900
rs772828681	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116797625	GGCTTAGACTGTGAG[A/G]GTTCTTGGCTTTGCC	84900
rs772831438	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838910	ACATATGACCAGGCC[A/G]GGCACACATTTTAGT	84900
rs772880181	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116809017	CCAAGGCCCACCCTT[C/T]TGTGGTTATAACTGG	84900
rs772895046	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116766576	CTGCTGCGAACCATG[A/G]TGTTCTCTTGCCTTT	84900
rs772974486	in-del	-/TTG			intron-variant	RNFT2	GRCh38.p7	12:116824929	ATGGTACTTTAGTTT[-/TTG]TTGTTGTTGTTGTTG	84900
rs772986773	snp	C/T			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736778	TGCTCCTTGCTGTTT[C/T]TCCCAGAAATTCTCA	84900
rs773027326	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116795410	AGACTCCATCTCCAG[-/A]AAAAAAAAAAAAAGA	84900
rs773037369	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116830680	GAGGCTGAAGTGAAG[A/T]AGGTGGATCACCTGT	84900
rs773054527	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116815056	TCTTAGTATGTCAAC[A/G]AGGGGCCCTGCATTT	84900
rs773114033	snp	G/T	9.69509e-05	0.00696176	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749981	GCTCGTTCCCCTCCA[G/T]CCTGGTGCTGGGCTC	84900
rs773141443	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829149	TGGGGCAGCTGAGGG[C/T]GGGTGGTTCAGGGAA	84900
rs773169806	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116760356	CCCTCCCCTGAGTTC[G/T]GGCCAGGAGGCTTCT	84900
rs773171555	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116817340	TTAAATAGAGACAGG[A/T]GGTCTCATGATGTCT	84900
rs773197325	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116742133	AGTCAGAGGGCAGAA[A/G]GGACCGAGGAAAAAG	84900
rs773207167	snp	G/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739510	AAGTGCTATGAATAA[G/T]ATAAAACAGGGCAAT	84900
rs773230319	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116803162	CAGAGAAGGAAGTTG[C/G]TCCATCTCATGAGCG	84900
rs773242755	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116793984	CTGAATTCAGAGTTT[A/C]TCTGGGTGCTGTGGC	84900
rs773250582	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116746287	ACTTCAGGTGCTGGG[A/G]CCCACCCATAAAGAT	84900
rs773251483	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771940	CTCACTCCCATGAAC[A/G]TCTCGAACGGTCAAC	84900
rs773261114	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116800368	CCGGGCACAGTGGCT[G/T]ACACCTGTAATCCCA	84900
rs773302760	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116751465	CTGGAGTGCAATGGC[A/G]CGACCTCTGCTCACT	84900
rs773306690	snp	C/T	3.3024e-05	0.00406336	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833812	GTTCTATCTGGTCAT[C/T]GAGGAGCTGAGCCAG	84900
rs773351449	in-del	-/GAGGAAGGTA			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737541	AAGGAGGAGGAAGGT[-/GAGGAAGGTA]AGGAAGGAAGGGAGG	84900
rs773378544	snp	C/T	3.46159e-05	0.00416014	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750087	CGCCTACCACCACCG[C/T]CAGCCCCACCACCAT	84900
rs773404644	snp	A/G	0.00032305	0.0127051	missense, intron-variant	RNFT2	GRCh38.p7	12:116849389	TGCCGCTCGGTCGCC[A/G]TGGACACCCTGCGCT	84900
rs773481492	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804699	AGGCAGGCTGGGTGC[A/G]GTGGCTCACGCCTGT	84900
rs773484178	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116761803	CTCCTCCACCCACCT[A/G]CAGACCCTCAATTAG	84900
rs773490776	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116846025	CTACCCCTTGGATCA[A/G]ACTGGTCCCTCTGTC	84900
rs773499355	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116770367	ATAGCCTAGATGTGT[A/G]GTAGGCTATGCTAAC	84900
rs773511701	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116822531	ATTAATAGCACCTGC[C/G]TCATAGTGGTGTGCA	84900
rs773519972	snp	A/T	1.65021e-05	0.00287241	intron-variant	RNFT2	GRCh38.p7	12:116754102	TGTGGCTGCTGCAAC[A/T]AATAAGCCACAAGCC	84900
rs773520494	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820702	TGGCACAAAGCCACT[C/T]TGGAAAATCAGGCTG	84900
rs773534095	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763673	AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA	84900
rs773542796	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803351	ATTTTTCATTTTTAG[A/G]TTATTTTTGAATATT	84900
rs773544932	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116753054	ATCTGCCTGGGTCAT[G/T]TTTGTCTGTTAGCTG	84900
rs773545208	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116800960	CAACTCAGCTTGACT[-/G]GGTGACAATAAGAAT	84900
rs773586612	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116742852	CTTTGGGAAGCCAAG[C/G]TGAGAGGATTGCTTG	84900
rs773607139	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825787	CAACCCCATTTACAG[A/G]TGAAGAAACTGAGGG	84900
rs773608148	snp	C/T	1.82747e-05	0.00302275	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737862	CACCCACCTCTTCCG[C/T]AGAAGCCGGCGCCAC	84900
rs773615783	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116847098	ATTTTTAGTAGAGAC[A/G]GGATTTCACCATGTT	84900
rs773630501	snp	A/C/T	0.000126978	0.00796715	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766869	TTCTGGCGGGGAACA[A/C/T]CCTCTATGTGCTTTA	84900
rs773633254	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811781	GGCTTGGCAGCCCAC[C/T]GAGGCTTTGCTGGCC	84900
rs773658518	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116773996	TTCTGACACATGCTG[A/C]AACATGGATGAAACT	84900
rs773693254	in-del	-/T/TT/TTT			intron-variant	RNFT2	GRCh38.p7	12:116753148	TCTTTTTTCTTTTTC[-/T/TT/TTT]TTTTTTTTTTTTTTT	84900
rs773703301	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116847531	CTTTCTCTCTCTCTC[-/T]CTTTTTTTTTTTTGA	84900
rs773714795	in-del	-/TTT			intron-variant	RNFT2	GRCh38.p7	12:116846903	TAGCATGCCCAGGAT[-/TTT]TTTTTTTTTTTTTTT	84900
rs773765296	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116795373	AGGTCACACCACTGC[A/C]CTCCAGCCTGGGCGG	84900
rs773823509	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116772915	CTCACTGTAACCTCC[A/G]TCTCCTGGGTTCAAG	84900
rs773860912	snp	A/G	1.64846e-05	0.0028709	splice-acceptor-variant	RNFT2	GRCh38.p7	12:116753982	CCTTCTCTGTCCCAC[A/G]GGCATTGCTGTGTGC	84900
rs773875655	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116757799	GAATGTGTATTCTGC[A/G]GTTGTCAGATGAAAT	84900
rs773879049	snp	A/G	5.61908e-05	0.00530021	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750307	TTTCAGCATAAGCTC[A/G]GTGAGTTCTGGGGGC	84900
rs773905995	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814844	CCACCATGCCCAGCT[A/G]AGTTTTCTATTTTTA	84900
rs773923381	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116784552	AGGCAAAGCAATGAG[A/G]CATAGTAGACCCATT	84900
rs773948689	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775370	TGTATGTGACACCAA[C/T]AACCATTATCTTGGC	84900
rs773991112	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738952	TATTTATATAATGAC[C/T]TTTTCTTGATATATG	84900
rs773991742	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798371	AGAGATTGTTCGGAT[A/G]AATACATAGAGAAAA	84900
rs773994194	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116827017	CCTGACTCAGGAGTT[C/T]GAGACCAGCCTGGGC	84900
rs774041410	snp	A/G	2.15158e-05	0.00327985	upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737765	GGAAGAAGGGAAGGG[A/G]AGGAGGGGAAGGGCG	84900
rs774041553	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116750706	TCATCTATCAAGTGG[G/T]GGTATGATTTTATAG	84900
rs774044938	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116810328	AAAGCCACAAGGGCA[C/T]GGCAGGAAGAGGGGA	84900
rs774108432	snp	A/G	1.65094e-05	0.00287305	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833826	TCGAGGAGCTGAGCC[A/G]GCTGTTCCGATCCCT	84900
rs774149295	in-del	-/GATG			intron-variant	RNFT2	GRCh38.p7	12:116789441	GGTGGATGGATGGTA[-/GATG]GATGGATGGATGGAT	84900
rs774196399	snp	A/G/T	3.36997e-05	0.00410474	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833909	AGCTACTTCCTGGGC[A/G/T]GGGTCCTGATCGTTC	84900
rs774198334	snp	C/G	0.000107015	0.00731409	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750000	GGTGCTGGGCTCCTC[C/G]GCTGGCGGCGGGGAC	84900
rs774221347	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116829771	TTTTTGGTAGAGACA[-/G]GGTTTCACCATGTTG	84900
rs774231628	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116767642	TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG	84900
rs774243350	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842298	AAGCAGGTCACTAGG[C/T]GCCACCCTTACTTAA	84900
rs774265052	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116799635	TGGATTTATCAAGGA[A/T]TTTTTAAAGGGATTC	84900
rs774275843	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116818524	GAGTGAGCAGTCTCT[A/T]AGCGATGGGAGAAAT	84900
rs774284743	snp	A/G	1.65233e-05	0.00287426	intron-variant	RNFT2	GRCh38.p7	12:116779173	TAAGGGAACCTTCTG[A/G]CTCTCTCAATCCTCC	84900
rs774298339	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116838503	ATCCACTTAGGCTGT[A/T]AGTATGCAGTATGAC	84900
rs774326384	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116770800	CTTGCCTCAAGTGAT[C/T]CACCCACCTCAGCCT	84900
rs774340448	snp	C/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736947	GGCACCCATGCGAGG[C/G]CTGGCCGACCCTCGC	84900
rs774340847	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116745167	GAGTTTCCTCCATTG[C/T]ACCAGATTTTTTTTT	84900
rs774344831	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116740207	AAAAGGAGTTTCAAG[C/G]GGGGATCACTGAGAG	84900
rs774370824	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116792113	GGAGTTCAGTGGCAC[A/G]ATTTTGGCTCACAGC	84900
rs774385954	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116822860	AAATTAGCCAGCCAT[G/T]GTGGTGCACGCCTAT	84900
rs774493788	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791506	AGAGAGATGGGGTTT[C/T]GCCATGTAGGCCAGC	84900
rs774512648	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768769	GAGTTTTGCCCTTGT[C/T]GCCCAGGCTGGAGTG	84900
rs774513141	in-del	-/ATTT			intron-variant	RNFT2	GRCh38.p7	12:116846901	ACTAGCATGCCCAGG[-/ATTT]TTTTTTTTTTTTTTT	84900
rs774569513	snp	A/C	5.15761e-05	0.00507793	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750094	CACCACCGCCAGCCC[A/C]ACCACCATTTCCACC	84900
rs774569656	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116790998	AAAATAAACCATTAA[C/T]CATTTTAGAGTATGC	84900
rs774579079	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820073	TCCTTGTTTCTTTTG[C/T]TTTTAAGGGATATTG	84900
rs774623019	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781290	AGGGGGCTGACCTGC[A/G]CGAACTATATCAATG	84900
rs774630188	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116834652	TGTTTCATATAAATG[A/G]AATCATGTAATAGGT	84900
rs774665414	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811622	CTCAAATAATCTGCC[C/T]GCCTTGGCCTCCCAA	84900
rs774683143	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116804887	TGGGAGGATTGCTTG[A/G]GCCTGGGAAGTAGAG	84900
rs774716663	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116821951	GCCATTCTCCTGCCT[C/T]AGCCTCCAGAGTAGC	84900
rs774719551	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116751647	CTCAGGTGTTCCATC[C/T]GCCTCAGCCTCCCAA	84900
rs774723275	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116814678	TGTTGCCGTATGATA[-/T]TTTTTTTTTTTTTCC	84900
rs774730332	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116815975	TCTCCCTCCTTCCCT[G/T]GCACCTCTCCCTCCA	84900
rs774748594	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831386	CACTGGGGATGTTAA[C/T]CTTGATCACCTGATT	84900
rs774763852	in-del	-/CAGA			intron-variant	RNFT2	GRCh38.p7	12:116787896	CTGTTTTTTGTGCTC[-/CAGA]CAGACAGACCCTACC	84900
rs774813747	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116848913	CAACCTCTGCCTCCG[G/T]GTTCAAACGATTCTC	84900
rs774830955	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839421	GGATGGGATGGGTGG[A/G]TGGGTGGATGGATGG	84900
rs774859552	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116764690	TGAGTTCAGCAGTTC[A/G]AGACCAGCTTGGCCA	84900
rs774912310	snp	C/G	3.94454e-05	0.00444085	upstream-variant-2KB, utr-variant-5-prime, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737947	GCGCGGAACGCGGCA[C/G]GCCCGGGTCCCGGGC	84900
rs774921465	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116849082	TCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGT	84900
rs774946976	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774272	TCATTGAACTGTGCG[C/T]GTAAAAATGGTTAAG	84900
rs774984251	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116775770	TAATTAGGCTGGGCA[C/T]AGTGGCTCACGCCTG	84900
rs774986086	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116763869	ATCTACCCAGAGGAA[A/G]AGAAGTCATTATACG	84900
rs775014608	snp	A/G	3.40454e-05	0.00412572	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849478	GACACCCAGAAGGAC[A/G]CCAAGGGTCAGCATG	84900
rs775038321	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116804940	CCACTGCACTCCATC[C/G]TGGGTGATGAAGTGA	84900
rs775039537	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116774212	AAAAGAGGTCTGTGG[A/T]TGGATAGTGGTGATG	84900
rs775048738	in-del	-/TTTTTTTTTTTTT			intron-variant	RNFT2	GRCh38.p7	12:116846437	ACCATGCCCAGCTAA[-/TTTTTTTTTTTTT]TTTTTTTTTTTTGTA	84900
rs775137932	snp	C/T	1.6498e-05	0.00287206	intron-variant	RNFT2	GRCh38.p7	12:116754086	TTCCGACCTAGTCTC[C/T]TGTGGCTGCTGCAAC	84900
rs775183279	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116814545	GCCCTGAGGTGGAAA[C/T]GTGCTTGGCAAGGTT	84900
rs775203647	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116838433	GGAAGAATTACTGGG[C/T]CAGAAGGCACACAGT	84900
rs775208940	in-del	-/GTCCTCTAGAC			intron-variant	RNFT2	GRCh38.p7	12:116771152	AAAATATTAACAGTG[-/GTCCTCTAGAC]GTTAAACATGTGGAT	84900
rs775229712	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116816090	GATAAGCTCATCCAT[A/C]CACCTGGGACCAGGA	84900
rs775240352	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116798613	AGTCTCTGTCACCCA[A/G]GTTGGAGTGCAGTGG	84900
rs775283253	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116827699	GTGGTGCCACAGACC[A/G]TATGGCCTGCAAAGG	84900
rs775295041	snp	A/G	1.69006e-05	0.00290689	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833911	CTACTTCCTGGGCGG[A/G]GTCCTGATCGTTCTC	84900
rs775369648	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810517	AAGTGATGAGCAAAC[A/G]GCAGTGGTTGGTATG	84900
rs775374759	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116747912	GGATGAACCCTCGGC[C/T]GGGCACGGTGGCTCA	84900
rs775390302	snp	A/G/T			intron-variant	RNFT2	GRCh38.p7	12:116757117	TTTTTGTGCATAAAG[A/G/T]TGTTCATAGTAGCCT	84900
rs775394322	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116758945	CCTCGATTATTCCCC[C/T]AAATATGTTTTCCAA	84900
rs775396476	snp	G/T	7.81891e-05	0.00625208	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750164	GTGGGGACCACCGGG[G/T]GCACTCGGAGGAGGG	84900
rs775426132	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116769545	TTTATGTCTTAAGTT[C/G]TAACAAAAAATTTTA	84900
rs775464697	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116760665	TTTCCCACTTCCGCA[G/T]TTGGGGCATTCGCAG	84900
rs775465674	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116841832	AAAAATATATATATA[A/T]AAATATATATATAAA	84900
rs775478129	in-del	-/TTTTTT/TTTTTTCT/TTTTTTT			intron-variant	RNFT2	GRCh38.p7	12:116850620	TTTTCTTTTCTTTTC[-/TTTTTT/TTTTTTCT/TTTTTTT]TTTTTTTTTTTTTTT	84900
rs775513239	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116820482	TACTGGATTGGCTGT[A/G]GTGGATATGGAACAT	84900
rs775531792	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116813398	CCAGGCCTTTGCAGT[A/G]GCTGTTCCCTGTGCT	84900
rs775550108	in-del	-/AC			intron-variant	RNFT2	GRCh38.p7	12:116762406	CCATCTCAAAACAAA[-/AC]AAAAAAAAACAAAGA	84900
rs775551131	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116780747	GTCCTAAGATGCCTC[C/G]CATTGACCCTCCCCA	84900
rs775571129	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800674	CAAAAAATTAGCTGG[A/C]ACTGTGGTGCGTGCC	84900
rs775604171	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116780241	TGACTTAACATGGTG[G/T]TCCCCAACCTTTTTG	84900
rs775648061	in-del	-/TGGA			intron-variant	RNFT2	GRCh38.p7	12:116789639	TGGGAGGAGAGTGGA[-/TGGA]TGGATGGATGGATGG	84900
rs775679111	snp	A/G	1.6722e-05	0.00289149	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749841	CCCCTTGGCACCCAG[A/G]AACCGCAGCCAGGCG	84900
rs775681513	snp	A/C	3.5434e-05	0.00420901	intron-variant	RNFT2	GRCh38.p7	12:116849494	CCAAGGGTCAGCATG[A/C]CCGGACCCAGCCCTG	84900
rs775687591	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116750909	TATATATATATATAT[-/A]TTTTTTTTGAGACAG	84900
rs775694641	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116785993	GGAGGCAGAGGTTGC[A/G]GTGAGCTGAGACCGC	84900
rs775744487	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739689	GACACATTAGAGGAA[C/T]AGAAGGGCCACTGTG	84900
rs775791503	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116795728	GAGAAACATAAAAGC[A/G]GGCCCTTCCCTAAGA	84900
rs775833142	in-del	-/TCT			intron-variant	RNFT2	GRCh38.p7	12:116847531	CTTTCTCTCTCTCTC[-/TCT]TTTTTTTTTTTGAGG	84900
rs775849133	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845398	TAGGAGAGAAGACGC[A/G]ATCAGTACTTACATT	84900
rs775860513	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116740308	CAGATTCAAGGTATC[G/T]CAGGGACTGTTCATC	84900
rs775885886	snp	C/T	5.08091e-05	0.00504004	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849418	CTGCTGGAAGGACGG[C/T]GCCACGTCCGCACAC	84900
rs775915870	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116822950	TGCAGTGAGCCAAGA[C/T]TGAGCCACTGCACTC	84900
rs776007412	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835818	CACTGTTGGGAAGGA[A/G]GAAGTGCAAATGAGA	84900
rs776075345	snp	C/T	2.58977e-05	0.00359836	intron-variant	RNFT2	GRCh38.p7	12:116741104	TGAAAGGTAGGCATC[C/T]CTGCTTCTGTTCCAT	84900
rs776165399	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116817125	TCAAGCGATTCTCAT[C/G]CATCAGCTTCCCAAA	84900
rs776169571	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835539	CCTTCCAGCAGGACT[A/G]GCAAGGCAATCCATG	84900
rs776200509	in-del	-/CTGTACAA	4.96545e-05	0.00498245	frameshift-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766904	TTCAGCTCCCAGCAG[-/CTGTACAA]CAGGTGAGCATGGGA	84900
rs776226531	in-del	-/TGGG			intron-variant	RNFT2	GRCh38.p7	12:116839414	GATGGATGGATGGGA[-/TGGG]TGGGTGGGTGGATGG	84900
rs776240695	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116766348	GACTTAAAACACAGC[C/T]CCTTGAGGTTTCTTA	84900
rs776277804	snp	A/G	0.00315955	0.0396206	upstream-variant-2KB, utr-variant-5-prime, synonymous-codon	RNFT2, C12orf49	GRCh38.p7	12:116737953	AACGCGGCAGGCCCG[A/G]GTCCCGGGCGGCATG	84900
rs776286581	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828938	GGATCACTTGAGCCC[A/G]AGAGATGGAGACCAG	84900
rs776302515	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116776436	CCAGGAAGGGCAAGA[A/G]CAGAGCTAAAGACGG	84900
rs776349555	snp	A/G	1.64961e-05	0.00287189	intron-variant	RNFT2	GRCh38.p7	12:116835926	ACGAGTGATCCTTGG[A/G]TACATTTCAGCCACC	84900
rs776380394	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116806107	TCATCTTGGCTGGGT[G/T]CTGAGGCTCATGCCT	84900
rs776419763	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832240	CCTCTCACCCCAGAC[A/G]ACCAGGGATCTGATT	84900
rs776432193	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116787337	CCATGGTGCCTTGAG[C/T]AAGTCGCTTAATGTG	84900
rs776450199	snp	A/G	2.03838e-05	0.00319241	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750248	TGATCTGCTGGCTCC[A/G]GAAAGGACTCCCCTT	84900
rs776451024	snp	C/T	3.7349e-05	0.00432124	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750168	GGACCACCGGGGGCA[C/T]TCGGAGGAGGGAGGC	84900
rs776460863	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116842873	GCCACTGTGCCCGGC[A/G]TGTTTATACTTTATA	84900
rs776498011	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116749281	ATCTCTTCCTCTTTC[-/C]CCCCCCACCACCCCT	84900
rs776505708	in-del	-/TTTTTC/TTTTTCC			intron-variant	RNFT2	GRCh38.p7	12:116850621	TTTCTTTTCTTTTCT[-/TTTTTC/TTTTTCC]TTTTTTTTTTTTTTT	84900
rs776516259	in-del	-/TTTG			intron-variant	RNFT2	GRCh38.p7	12:116842568	TATTTTATTTATTTA[-/TTTG]TTTGTTTGTTTGTTT	84900
rs776516649	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116744746	AATCTCGGCTGGATG[C/G]AGGGGAGAGGCCCAG	84900
rs776528264	snp	A/G	3.29468e-05	0.00405861	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779292	AAGTACATCACCATC[A/G]CCCTCAAGTGCCTCA	84900
rs776565509	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116799446	TATGATCTAGATGTG[A/C]TATTTCATTACCTTC	84900
rs776583188	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842072	CCAGGGCTGTGGTCC[C/T]CTCCTGGCTCAACTT	84900
rs776596783	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116759408	TGCTGGTGAACTAGT[A/G]TGATTTTGGGGGAGT	84900
rs776622235	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116832625	ATTCAACTTTATTAG[A/G]CACTACAGAGTGGGT	84900
rs776630131	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116749817	TGCCTGACTTCCTGG[G/T]GTTTCTCTCCCCTTG	84900
rs776646720	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116785676	GAGCTCTGTAAACGG[C/T]GAGTAAGTGAAATGG	84900
rs776648903	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116803254	CCTCTGGGTGCAACC[A/G]ACACCACCTGCCACG	84900
rs776700389	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116770451	GGATGTGTTTCTCAG[A/C]ACATGTCCCAGTCAT	84900
rs776720013	snp	C/T	0.000192105	0.00979874	intron-variant	RNFT2	GRCh38.p7	12:116748645	CACATTACTCTCTGC[C/T]GCCCACCCAATGTCA	84900
rs776728911	snp	A/G	1.64814e-05	0.00287061	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852603	CAAAGGGAAGCAACA[A/G]GAACTTCTGCAACTG	84900
rs776753826	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116769753	AATAAATGTAACGGC[C/T]GGGCATGGTGGCTCA	84900
rs776770386	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116834042	ATACCCATGCTGATT[G/T]ATTTATTTATTTATT	84900
rs776884080	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116760811	TGCGAGCTGCCGCCC[A/G]CTGCTCTCTCTGGAG	84900
rs776888743	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116772233	AAGTGCTGGGAATAC[G/T]GGCATGGGCCACCAC	84900
rs776898350	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116814734	ACTGCTGGAGTGTGC[A/G]GTGGTGCAATCTCGG	84900
rs776918331	snp	A/C	1.64841e-05	0.00287085	intron-variant	RNFT2	GRCh38.p7	12:116779192	TCTCAATCCTCCCCC[A/C]AGCCTCATATTCCTG	84900
rs776921941	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116762224	CTCTACTAAAAAGAT[-/A]ACAAAATTAGCCAGC	84900
rs776923817	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116791595	AATTACAGGCATGAG[C/G]CACCATGCCCGGCTT	84900
rs776944944	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116803396	TATTTCAACTATACA[G/T]AAAATAATATATAAT	84900
rs776967383	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116802216	TCACATAGTAAAGGC[G/T]CTGAGAAGTCCCGCA	84900
rs776970219	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116754592	CGGTTGTACTAGTTT[A/G]CATTCCCACCAGCAG	84900
rs777010712	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794664	AGGAAGGAAGGAAGG[A/G]AGGAAGGAAGGGAGG	84900
rs777024113	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116845849	ATCAGCTATCTTCAA[A/G]TGCCTCAAACATCTT	84900
rs777049517	snp	C/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116753996	CAGGCATTGCTGTGT[C/G]CATCGGGATGGCCAG	84900
rs777057051	in-del	-/AAAA			intron-variant	RNFT2	GRCh38.p7	12:116845245	CAAGACCCGGTTTCA[-/AAAA]AAAAAAAAAAATATA	84900
rs777077460	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844896	TAGATATTTACTGAG[C/T]ATCTGAGCAAGAACC	84900
rs777078027	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824758	CATGTCTCTTCCTAT[A/G]AGGGAACCAATCCCA	84900
rs777111747	in-del	-/AAAAA			intron-variant	RNFT2	GRCh38.p7	12:116806369	AGTGAGACTGTCTCA[-/AAAAA]AAAAAAAAATATATA	84900
rs777123741	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116810091	ATATTGGACACCCCA[A/G]AGTGCCGAGACCTAT	84900
rs777150392	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116780510	TCACCTCCTGCTGTG[C/T]GACCTGGTTCCTAAC	84900
rs777190855	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116820910	TAAACTAGAAGCCAG[-/C]CCTAGTCCTTCTCTC	84900
rs777211877	snp	C/T	7.83116e-05	0.00625697	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836201	TGGAGTCCGAGCCAC[C/T]GGGCAGCAGTGCACA	84900
rs777237900	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116821203	CTGCCCCCAGCCCCA[C/T]TTCCCCCTCCTGTTT	84900
rs777258812	in-del	-/TATATATATA			intron-variant	RNFT2	GRCh38.p7	12:116750882	ATATAATATATATAT[-/TATATATATA]ATATATATATATATA	84900
rs777267449	snp	C/T	9.34623e-05	0.00683538	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749969	GCCTCCCCACCAGCT[C/T]GTTCCCCTCCAGCCT	84900
rs777270258	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116768421	TGGCCTTTTATATTA[C/T]AGTCATGTGTCACGT	84900
rs777276989	snp	A/G	6.60939e-05	0.00574827	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779341	TCATCCTGGCTGTCA[A/G]GTCCAAGGTAGGCAC	84900
rs777309182	in-del	-/GAGATG			intron-variant	RNFT2	GRCh38.p7	12:116802006	TTTGTATTTGTAGCA[-/GAGATG]GAGTTTCGCCATGTT	84900
rs777356378	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116800657	AAAATGGTTTAAAAA[A/T]GCAAAAAATTAGCTG	84900
rs777411951	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116833540	GGTTTCTCCTACCCT[A/G]AAACTCGATCCTCAA	84900
rs777437208	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116750908	TATATATATATATAT[A/T]TTTTTTTTTGAGACA	84900
rs777465666	snp	A/G			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737654	GGGAAGGGGAGAAAG[A/G]AAGGAAGGGAAGGGG	84900
rs777467199	snp	A/G	0.000591424	0.0171861	intron-variant	RNFT2	GRCh38.p7	12:116748734	GAGCCAGCGGTCCTT[A/G]GGATCCCGAGGTAAT	84900
rs777469388	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116779967	TAGTGATTGCCAGTG[A/G]CTCTGTAAGGTGACC	84900
rs777535875	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116790022	GTAATAACTCACTAC[C/G]TCCTCTTACAGCAAC	84900
rs777537480	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116831789	ATGAGTTTTGGCAAA[C/T]GTGCGCACCCATGTA	84900
rs777540224	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116847303	CCTTTATAGCTGGCA[-/T]TTTTTTTTGCCACCC	84900
rs777555731	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116749435	GGCATGCGCCACCAT[A/G]CCTGGCTAATTTAGC	84900
rs777561990	in-del	-/TTCA			intron-variant	RNFT2	GRCh38.p7	12:116809192	AGCTGAGTTTGTTCA[-/TTCA]TTCATTCATTCATTC	84900
rs777564958	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116772675	AAAACACCTCCAATT[C/G]TGTCACCTAACAGCA	84900
rs777626161	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116825172	CTGGTTTTCATGTTT[C/T]TCCTCCAATTAGTCT	84900
rs777679832	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116849936	GCAACCTCCACCTCC[C/T]GGGTTCAAGCGATTC	84900
rs777720261	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116792077	TTTGTTTTTTGAGAC[-/AG]AGTCTCTGTTGCTCA	84900
rs777757647	snp	A/G	3.52392e-05	0.00419742	upstream-variant-2KB, synonymous-codon, missense	RNFT2, C12orf49	GRCh38.p7	12:116737820	GCTGAGGAAGTAGAC[A/G]AGCGACAGCCCGAAG	84900
rs777758003	snp	C/G/T	0.000121148	0.00778216	intron-variant	RNFT2	GRCh38.p7	12:116766802	ATCACATATCTCTTG[C/G/T]TTTGTCTTCAGGAGA	84900
rs777778919	snp	A/G	1.66618e-05	0.00288628	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833892	GTGACGACTCCTCCA[A/G]CAGCTACTTCCTGGG	84900
rs777850378	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116807270	CAAGTCTGTGGCCAG[A/G]CTGTGACTTCAGAGG	84900
rs777883044	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749306	ACCCCTTTTGAGACA[C/G]GCTCTCTGTCGCCCA	84900
rs777913053	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116813300	CCTTCGCCTCTCTTC[C/G]CAGCCCGACACCTCA	84900
rs777931969	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116795331	AAGAATCGCTTGAAC[A/C]CAGGAGGCAGAGGTT	84900
rs777959807	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116745278	CTCCCCGGTTCAAGC[A/G]ATTCTCCTGCCGCAG	84900
rs777967909	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116828352	TAACCAGCTCCCAGG[C/T]GATGCTGATGGTGCT	84900
rs778002242	snp	C/T			utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116852501	TTACAATCCCACTTG[C/T]CTGAATAATCAAGTG	84900
rs778007665	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116850422	TCCTGTCCTGGCCTC[A/G]CAAAGTGCTGAGTGC	84900
rs778080195	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116815715	CTTTCGCCCTGTAAG[G/T]TACCAAATTCATAGG	84900
rs778088946	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842440	GCTGTGTACCTTGGG[C/T]GCACAGCTCCCCCTC	84900
rs778095251	in-del	-/ACCA			intron-variant	RNFT2	GRCh38.p7	12:116749288	CCTCTTTCCCCCCCC[-/ACCA]CCCCTTTTGAGACAG	84900
rs778117993	in-del	-/AGG			intron-variant	RNFT2	GRCh38.p7	12:116789414	GGATGAGTAAATGGT[-/AGG]AGAGTGGTGGGTGGA	84900
rs778129696	snp	A/C	0.000194515	0.00985999	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750144	CTCCCTGCTGCAGCA[A/C]GTGGGTGGGGACCAC	84900
rs778132458	snp	C/T	2.72387e-05	0.00369034	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750202	GAGCAGCCTGGGACG[C/T]CCGCCCCCGCCCTGT	84900
rs778134758	snp	A/G	6.13422e-05	0.00553781	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737915	TCCCGGCGCGGACGT[A/G]GGGCGCGGCGGCCGG	84900
rs778161907	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116758855	GCAAAGACCTTTTTG[C/T]GATGAATTTCCCGGG	84900
rs778190233	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116775189	CGCCTGAACCGGGGA[A/G]GTAGAGGTTGCAGTG	84900
rs778192255	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116787988	GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC	84900
rs778201442	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116846384	CAAGCAATCCTCCCA[-/C]CCACTTCAGCCTCCC	84900
rs778202197	in-del	-/TTTG			intron-variant	RNFT2	GRCh38.p7	12:116848807	TTCTCCCTCCTGCTT[-/TTTG]TTTGTTTGTTTTTTG	84900
rs778261476	snp	C/G	3.3998e-05	0.00412284	utr-variant-3-prime, intron-variant	RNFT2	GRCh38.p7	12:116849468	GAACACTGAGGACAC[C/G]CAGAAGGACGCCAAG	84900
rs778277779	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116760747	GTCTGTGGGTCCTCT[C/T]GGGATTGCTGGTTTG	84900
rs778287663	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799135	CAGTTCTGTGTGATC[A/G]TAGGACTTGAGGTCC	84900
rs778317054	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116786814	AGCGGGGCTGCACTG[C/T]CTCCGGAGGCTCAAG	84900
rs778345040	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116841401	GAGGCTGCAGTGAGC[C/T]GAGATTGCACCACTA	84900
rs778351462	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813738	TTCATGAGAATGTTG[C/T]AGATATTTCTCCCTT	84900
rs778361501	in-del	-/GGGGCGCGGCGGCC	5.60742e-05	0.00529471	upstream-variant-2KB, utr-variant-5-prime, frameshift-variant	RNFT2, C12orf49	GRCh38.p7	12:116737915	TCCCGGCGCGGACGT[-/GGGGCGCGGCGGCC]GGGGCGCGGAACGCG	84900
rs778422100	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116781586	TTGAGCGTTCTCTCC[C/T]CTCTCCCTCTCCCTC	84900
rs778474820	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116811026	AGCTGGAATTTTGGT[C/T]CCACCATTTCCATCA	84900
rs778506097	snp	C/T	6.64695e-05	0.00576457	intron-variant	RNFT2	GRCh38.p7	12:116766937	TGGGAATCCAACCCC[C/T]ACGGTGGGAGAGTGG	84900
rs778529515	in-del	-/GAGGAAGG			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737541	AAGGAGGAGGAAGGT[-/GAGGAAGG]TAAGGAAGGAAGGGA	84900
rs778562038	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116842474	TGAGTCTCACTGACC[C/T]GTCTGTTTGCTGTTA	84900
rs778597524	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116821315	CCCACCCCTCCTGGC[C/T]GGGCGCTGCTGTGAA	84900
rs778612690	snp	C/T			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116738930	GAGATTGCAAATTCT[C/T]GAAAAATATTTATAT	84900
rs778626639	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116749618	AGTCACACTGGATTG[C/G]GACCCACTCCAGTGA	84900
rs778665392	snp	A/G/T	3.30203e-05	0.00406316	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833835	TGAGCCAGCTGTTCC[A/G/T]ATCCCTTGTCCCCAT	84900
rs778709118	snp	A/G	0.000295508	0.0121518			GRCh38.p7	12:116750066	AGGGGGCCGGGGCGA[A/G]GGGGGCGCCTACCAC	84900
rs778733278	snp	C/T					GRCh38.p7	12:116751079	GCCACCACACCCGGC[C/T]AAATTTTAAATTTTT	84900
rs778734330	snp	G/T					GRCh38.p7	12:116764131	TTTGTATGTTCTCAC[G/T]CATAAGTGGTAGCTA	84900
rs778735680	snp	A/T					GRCh38.p7	12:116835059	TTTACCATGTTGGCC[A/T]GGCTGGTCTCAAACT	84900
rs778756445	snp	A/C					GRCh38.p7	12:116795062	TATACTCCTACTTCT[A/C]TAATACTAATACTAA	84900
rs778787133	snp	C/G	2.01072e-05	0.00317068	upstream-variant-2KB, utr-variant-5-prime, missense	RNFT2, C12orf49	GRCh38.p7	12:116737933	GCGCGGCGGCCGGGG[C/G]GCGGAACGCGGCAGG	84900
rs778898908	snp	A/G	0.000169693	0.00920965	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766849	CATCTTGTGGATCCT[A/G]GCCTTTCTGGCGGGG	84900
rs778922397	snp	C/G	1.65943e-05	0.00288043	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750161	TGGGTGGGGACCACC[C/G]GGGGCACTCGGAGGA	84900
rs778924468	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116835965	CTCCTTTCAGTCCTT[C/T]GACATCTGTGGACGT	84900
rs778934113	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116804313	AAAGCCTCAGACCCC[A/T]CCCCAGACCTACTGA	84900
rs778998087	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116783028	AGGGCTGGCCTGGCT[C/T]ATCATAAGTGCTCAA	84900
rs779000739	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116752615	AGGTACGGTGGCTCA[C/T]GCCTGTAATCCTGGC	84900
rs779002841	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116836972	ACAGCTACTTCATAG[C/G]GCTATTATTATGATT	84900
rs779015350	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741344	AATTTTGATTTATAG[A/G]GATGTCTTAGTCCAT	84900
rs779015555	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116824276	GAAACCCAGCTGTTT[A/C]AAAGCACAAGGCCAT	84900
rs779042183	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116747215	GTGCGTGCCACCATG[C/G]CTGGCTACTTTTTAA	84900
rs779066298	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807458	AACAATCCTATGAGG[C/T]AGACACTCTTAATGC	84900
rs779110439	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116851779	AAGGGAGGGAGGGAG[A/G]AAGGAAGGAAGGAAG	84900
rs779120574	snp	A/G	1.95888e-05	0.00312954	intron-variant	RNFT2	GRCh38.p7	12:116833979	GGGCCGGCCTAAGGA[A/G]GGCCCCATTCACTAG	84900
rs779121436	snp	C/G/T			intron-variant	RNFT2	GRCh38.p7	12:116817739	AAGTATGGAGTAAGA[C/G/T]CACACTTTACACTCA	84900
rs779143098	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116808486	CTGCCACCAAGGGAC[A/G]CAGCAGGGACAGGGC	84900
rs779147206	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116838283	CCTGGGCCCATCGTG[C/T]TGATTAAAGGTTAAT	84900
rs779158224	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116803106	TCTTAAAAAAAAAAA[-/T]CAAAAACAAATACAC	84900
rs779182607	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116834851	TACTATTATTACTCC[-/T]TTTTTTTTTTTTTTT	84900
rs779227298	in-del	-/CCCTGCTGCAGCACGTGGGTGGGGACCA	5.54124e-05	0.00526338	frameshift-variant, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750131	GCCACCGCGGGGGCT[-/CCCTGCTGCAGCACGTGGGTGGGGACCA]CCGGGGGCACTCGGA	84900
rs779301778	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116789239	GGGAGGAGAGTAGAT[A/G]GATGGGTGGATGGGT	84900
rs779369781	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116765808	TTGGATTTAATTCTA[C/T]ACTGTGGCATTCCAT	84900
rs779374430	snp	C/T	3.29473e-05	0.00405864	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779261	ATGGATTGTGGGGAT[C/T]GCAGACTTTGTTCTG	84900
rs779382959	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116759925	GAACTCTCGAGTTTC[C/T]ATGGCCTTTGTCTTC	84900
rs779382988	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116745569	CCTGGCCTCACTAGG[A/T]TTTTAGTAACATACC	84900
rs779386612	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116757759	TATAGTCTATCTTGG[-/A]GAAAGTTCCATGCGC	84900
rs779397194	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116787717	ATGTTGTCTCTAAAA[-/G]GAAAAAAAAAAAAAA	84900
rs779407495	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116800648	CAAAAAAAAAAAATG[A/G]TTTAAAAATGCAAAA	84900
rs779423913	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116777248	CACAGTACCTACTTC[A/G]TAGAGTCTTTGGGAA	84900
rs779449138	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116766045	GGGAGCCCAAGGCAG[A/G]AGGATCACTTGAGGC	84900
rs779488948	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116837583	TTGTTTTTCATGTTC[-/A]ATTGTATTTCTTTTT	84900
rs779502917	snp	A/G	7.20046e-05	0.00599976	synonymous-codon, intron-variant	RNFT2	GRCh38.p7	12:116849442	CGCACACTTCCAGGT[A/G]TACTAGGACCGAACA	84900
rs779502982	snp	A/G	8.41255e-05	0.00648504	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116766859	ATCCTGGCCTTTCTG[A/G]CGGGGAACACCCTCT	84900
rs779512115	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116799971	GTGGTACCCTCCCCA[A/G]GGTGATGAGTGAGTT	84900
rs779514882	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813081	CTGCCTCAGCCTCCC[C/T]GATAACTGGGACTAC	84900
rs779524713	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116844232	GTTTTTTTTTTGTTT[C/T]GTTTCATTTTGTTTT	84900
rs779532614	in-del	-/AGGA	0.00141283	0.0265409	intron-variant	RNFT2	GRCh38.p7	12:116851777	AGAAGGGAGGGAGGG[-/AGGA]AGGAAGGAAGGAAGG	84900
rs779570359	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116788390	CTGCCCTGTCTCCCA[C/G]CTGCACCTACTGATT	84900
rs779570382	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116801369	GCCAGGAAGATTCTA[C/G]AGCATGTAGCAAGAA	84900
rs779572915	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116828664	GAGGGAAGAAGAAAG[G/T]GAGTGGGCAAGGAAG	84900
rs779575246	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116843980	CCACCTAGAGGGCAG[C/G]GCAGATGTTGACTAA	84900
rs779637939	in-del	-/AAAAA			intron-variant	RNFT2	GRCh38.p7	12:116845244	GCAAGACCCGGTTTC[-/AAAAA]AAAAAAAAAAATATA	84900
rs779662794	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116843982	ACCTAGAGGGCAGGG[A/C]AGATGTTGACTAAGC	84900
rs779681589	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116829991	CATTCTCTATTATTT[C/T]CATTTGGAACAATAA	84900
rs779694840	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116811450	GGGCCATCTCGGCTC[A/T]CTGCAACCTCTGTTT	84900
rs779715475	in-del	-/TTTC			intron-variant	RNFT2	GRCh38.p7	12:116804526	TGAGCAATTAGATTG[-/TTTC]TTTATTTTTTTACCA	84900
rs779748319	in-del	-/AAAAAAAAAAAAAAA			intron-variant	RNFT2	GRCh38.p7	12:116771461	TGAGATCCTATCGTT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84900
rs779895591	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116805595	GTCTCGTGCCTCAGC[C/G]TCCTGAGTAGCTGGG	84900
rs779904694	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116782760	CTTTCTCACATGCCG[A/T]AAATAAGTCTGAACA	84900
rs779904817	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116770427	TCACACAAGGACCAG[A/G]TCACCTAAGGATGTG	84900
rs779979302	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116826335	TCCAAGCAGAGAACC[C/G]TCCATGCCCAAGCAC	84900
rs780029134	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781694	ACACTGGCCCCACCC[A/G]AATAATCTAGGCTCA	84900
rs780038036	snp	C/T	2.47626e-05	0.00351862	intron-variant	RNFT2	GRCh38.p7	12:116741017	GGAGACTCTGGCTCA[C/T]CCATGTGTTGGGTTT	84900
rs780057411	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773493	TCTTGGCATGACTTA[A/G]CCGTTCACTGGCAGT	84900
rs780077850	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116793724	TGTCTCCTTCCCATC[A/G]CTTGGATCTCGACTC	84900
rs780089083	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116827441	GTGTCCTTAAGCAAC[C/T]GAAAGACAGGGAAAG	84900
rs780103371	snp	C/T			intron-variant, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836405	CGGTTAAGACCGGAG[C/T]CAGCCAGACCTGGGT	84900
rs780108123	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116772826	GTCAACAAATGCAAG[A/G]AGCATTTCTTTATTT	84900
rs780118794	snp	A/G/T	3.30094e-05	0.00406249	intron-variant	RNFT2	GRCh38.p7	12:116753940	ACCTGGGCTAGGCCT[A/G/T]ATGAGTCTAAGTGGG	84900
rs780142237	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116824756	CTCATGTCTCTTCCT[A/G]TAAGGGAACCAATCC	84900
rs780154323	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116835229	TGCCCAAGGTCACTC[A/G]GGTAAAGACAACAGA	84900
rs780156470	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116849627	TCATCTTCCTCTCTC[A/G]TTCTGTGGTATAGTG	84900
rs780186129	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116785674	CAGAGCTCTGTAAAC[A/G]GTGAGTAAGTGAAAT	84900
rs780195961	in-del	-/AG			intron-variant	RNFT2	GRCh38.p7	12:116806395	AATATATATATATAT[-/AG]ATATAGATAGATAGA	84900
rs780262406	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116807875	TTGATGCGATTGTGG[C/T]TCACTACAGCCTCAA	84900
rs780270286	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116839601	TAGGATGGATGGACA[C/G]ATGGACGGATGGATG	84900
rs780286268	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116825329	TTAAGGCCTAGGCTT[A/G]GAAGTCCCAGATATC	84900
rs780289649	snp	A/T			intron-variant	RNFT2	GRCh38.p7	12:116779464	ATGTCAGCATATAAA[A/T]TAAACAGAGCCTGAG	84900
rs780312940	snp	C/T	3.53226e-05	0.00420239	intron-variant	RNFT2	GRCh38.p7	12:116836162	CCATAGCTGTATTTG[C/T]TTCTCCCCTCCCTCA	84900
rs780338462	snp	A/T	0.000159046	0.00891614	intron-variant	RNFT2	GRCh38.p7	12:116851931	CCTGTGGACATTGCC[A/T]TCCCCTCTGGTAGCC	84900
rs780393115	snp	C/T			utr-variant-3-prime	RNFT2	GRCh38.p7	12:116853493	CGGGCTGCTGAGACT[C/T]GGGATTAGAAGAAAG	84900
rs780428787	snp	A/C	1.64855e-05	0.00287097	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852727	AGGAAATAGAACAGT[A/C]TGCTGGGAGTCAGAC	84900
rs780476622	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116767276	ACCCAGGCTGGCAGT[G/T]GTGTGATCATGGCTC	84900
rs780498327	in-del	AAAAAAAAAAAAAAAA/T			intron-variant	RNFT2	GRCh38.p7	12:116771479	AAAAAAAAAAAAAAA[AAAAAAAAAAAAAAAA/T]TACGTATATGAGCAA	84900
rs780503951	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754174	ATTCTTATGCCTTTG[C/T]GTCCTCATAGCTTAA	84900
rs780517216	snp	A/C	0.000218047	0.0104392	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116749937	CCCACCAGCGCTCTT[A/C]TCGGGCTTATCAGGC	84900
rs780525030	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116779235	GAGATGCTGGACTTC[C/T]TTGACCTGCTATGGA	84900
rs780528415	snp	C/T	1.67809e-05	0.00289658	intron-variant	RNFT2	GRCh38.p7	12:116779380	GCCACAAGGTAGCCC[C/T]AGTCACATGGATCAT	84900
rs780546118	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116807611	CCATTCCCCACTCGC[A/G]CTCCCCTGACCCAGA	84900
rs780559130	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116754648	ATTCACACTAGCATC[C/T]ATTGTTTTTTGACTT	84900
rs780594813	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748044	AAAATACAAAAATTA[A/G]CCGCACATGATGGCA	84900
rs780604976	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116778411	GTGAGGGTGGGTTCT[C/T]ATAAAGCCAAGACGC	84900
rs780610428	in-del	-/AGA			intron-variant	RNFT2	GRCh38.p7	12:116776937	TTTTTTTTTTTTTTG[-/AGA]AGGAGTCTCACTCTG	84900
rs780616652	snp	A/G	4.9652e-05	0.00498232	missense, nc-transcript-variant	RNFT2	GRCh38.p7	12:116833865	TCCAGCTGTGGTACA[A/G]ATACATCATGGGTGA	84900
rs780616689	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116748083	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	84900
rs780644913	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116818770	AGCAAGTAACTTGAC[C/G]TCTCCGAGCCTTGTG	84900
rs780650482	in-del	-/CT			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116736453	CTTACAACACTCAGC[-/CT]CTCTGTTTGCCTAAG	84900
rs780667432	in-del	-/ACCAGAAGTC			intron-variant	RNFT2	GRCh38.p7	12:116775327	GTCCTTACTGAAGTC[-/ACCAGAAGTC]ACCAGTCTAGACGGT	84900
rs780669317	in-del	-/GT/GTT			intron-variant	RNFT2	GRCh38.p7	12:116776915	TCAGCTCAAAATGGG[-/GT/GTT]ATTTTTTTTTTTTTT	84900
rs780671970	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831655	ATTGTTAGAGTAAAG[A/G]TTATACATATTTTTA	84900
rs780674943	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116763669	CTGTAGTCCCAGCTA[C/T]TCGGGAGGCTGAGGC	84900
rs780712213	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116791884	ATTTCACATGCCCAG[C/T]GGAAGAAAATGAAAA	84900
rs780715226	snp	A/G	0.00013138	0.00810388	intron-variant	RNFT2	GRCh38.p7	12:116851826	AGCTTTGGCCCAGAT[A/G]TGGTTACCCCTTGGT	84900
rs780716001	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116778671	CCTCGCCAACATGGC[A/G]AAACCCTGTCTCTAC	84900
rs780726104	snp	A/C	0.000190313	0.00975296	intron-variant	RNFT2	GRCh38.p7	12:116748670	ATGTCAGCTGTGACC[A/C]AGGCTGGCCCCTCTG	84900
rs780767187	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116791025	ATGCCATTCAGTGGC[A/G]TTTAGTACATTCACA	84900
rs780834417	snp	A/G	1.72546e-05	0.00293718	intron-variant	RNFT2	GRCh38.p7	12:116766951	CCACGGTGGGAGAGT[A/G]GGGCACTTGGCTGGG	84900
rs780840602	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116845364	GCTTTGAGAGGGGTT[C/T]TCACCAGGAAGAATG	84900
rs780844973	in-del	-/G	0.00118304	0.0242924	intron-variant	RNFT2	GRCh38.p7	12:116851827	CTTTGGCCCAGATGT[-/G]GGTTACCCCTTGGTC	84900
rs780864703	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116838331	AACTGCTCCTGGCAC[A/G]TGGTCAGGGTTCAAT	84900
rs780865132	in-del	-/AAATA			intron-variant	RNFT2	GRCh38.p7	12:116806380	CTCAAAAAAAAAAAA[-/AAATA]TATATATATATATAT	84900
rs780886663	snp	G/T	1.65048e-05	0.00287265	intron-variant	RNFT2	GRCh38.p7	12:116753946	GCTAGGCCTGATGAG[G/T]CTAAGTGGGTGACAT	84900
rs780907792	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116802285	TTCCAACTTATTAAG[C/G]ATGGGACCCTTTTAT	84900
rs780915662	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830158	CTTCCCCTAATGTTG[A/G]TATCTGATATACCAG	84900
rs780919211	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116800670	AATGCAAAAAATTAG[A/C]TGGCACTGTGGTGCG	84900
rs780965066	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116801601	TAACACAAGTCAAGT[C/G]CTGGCTGGTTAGTTA	84900
rs780978722	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116782967	GGACCCTACTCACTC[C/T]ACCATGAGACTTCCC	84900
rs780993516	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116772646	AAATTGGAAAACCCA[C/T]TTAAAAAGGACCAAA	84900
rs781018133	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116813196	ACTCTTGGTCTCAAG[C/T]GATCCACCCACCTTG	84900
rs781074392	snp	A/C			intron-variant	RNFT2	GRCh38.p7	12:116760266	AAAACCTGCCCCAGA[A/C]TATCCGCCTCCCAGC	84900
rs781080639	snp	C/T	1.64917e-05	0.00287151	stop-gained, nc-transcript-variant	RNFT2	GRCh38.p7	12:116836193	AAGAACTATGGAGTC[C/T]GAGCCACCGGGCAGC	84900
rs781092237	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116740129	TGAGGCAGGAGAATC[C/G]CTTGAACCTGGGAGG	84900
rs781139911	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116771776	GGGAGGCAAAGCACA[A/G]GAAATTGAATGGATT	84900
rs781168947	snp	G/T	6.10184e-05	0.00552318	synonymous-codon, downstream-variant-500B	RNFT2	GRCh38.p7	12:116836276	GCCTCTGATTCTCCT[G/T]TGCCAGGTGAGCAGG	84900
rs781205884	in-del	-/GA			intron-variant	RNFT2	GRCh38.p7	12:116752198	CTACTGAAAAAAAAA[-/GA]GAGAGAGAGAAAGCT	84900
rs781234458	in-del	-/AAAAAA			intron-variant	RNFT2	GRCh38.p7	12:116806368	GAGTGAGACTGTCTC[-/AAAAAA]AAAAAAAAATATATA	84900
rs781235017	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116781906	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	84900
rs781259513	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116773904	AGCAACCCAGTGTCT[A/G]TTGACAGATGAATGG	84900
rs781272652	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116816569	AGTGAGTGTCCAGTT[A/G]TCTAGTGGCAGATGT	84900
rs781285505	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116838072	TGCTGTTTTCTGCAC[C/G]TTCCTTTTTAACTTA	84900
rs781289279	snp	G/T	1.64882e-05	0.00287121	utr-variant-3-prime	RNFT2	GRCh38.p7	12:116852733	TAGAACAGTCTGCTG[G/T]GAGTCAGACCTGGAA	84900
rs781305378	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116850395	TCTCAAACTCCTGGG[C/T]TCAAGCAATCCTCCT	84900
rs781325875	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116814076	CATGACCCCAGCCCT[-/C]CCCCGTGTCATTCTC	84900
rs781343511	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116757462	TGTAAGCATTTAGGG[C/T]TATGAGCTTTCCTAT	84900
rs781352982	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116804502	TTATTCATCCATTCC[C/T]CTAACTCATGAGCAA	84900
rs781371897	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116830773	AAATTAGCCGGGCAT[A/G]GTGGTGTGTAATCCC	84900
rs781375273	snp	A/G	1.6748e-05	0.00289374	intron-variant	RNFT2	GRCh38.p7	12:116833748	AGCTGGGTCCTTTGG[A/G]TCTTTACTGCTAATA	84900
rs781424998	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828351	CTAACCAGCTCCCAG[A/G]CGATGCTGATGGTGC	84900
rs781459006	snp	C/T	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116754030	CTTCGCCTATGCCAA[C/T]TCCACGCTTCGAGAA	84900
rs781483044	in-del	-/CCA	1.79361e-05	0.00299462	upstream-variant-2KB, cds-indel	RNFT2, C12orf49	GRCh38.p7	12:116737850	GACCAGGGCGAGCAC[-/CCA]CCTCTTCCGCAGAAG	84900
rs781498903	in-del	-/TGGATGGG			intron-variant	RNFT2	GRCh38.p7	12:116788979	GGATGGATGGATGGA[-/TGGATGGG]TAGATAAATGAGAGG	84900
rs781506349	snp	C/G			intron-variant	RNFT2	GRCh38.p7	12:116825702	GGCCTTTTCTTTCCC[C/G]CAGAGACCTAGTTTT	84900
rs781550721	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116744097	CCAGTGTGGTGGCAG[A/G]TGCCTGTAGTCCCAG	84900
rs781577434	snp	C/T	1.81965e-05	0.00301628	intron-variant	RNFT2	GRCh38.p7	12:116833951	TGCAAGGTGAGGTGG[C/T]CCCAAGGCTGGAGGG	84900
rs781650632	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116772473	ACCACGCCCGGCTGA[-/T]TTTTTGTATTTTTAG	84900
rs781691874	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116839698	TGAGTGACAGTGTGG[A/G]TGAGCAAATGAATGG	84900
rs781703385	snp	G/T			intron-variant	RNFT2	GRCh38.p7	12:116779869	GGCCTCCAGGCAGGT[G/T]TTGGAATGAAGAGGC	84900
rs781708193	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116798152	AGAGGAAAGATCACG[C/T]GAGGACACAGAGAAA	84900
rs781722123	snp	A/G	5.85086e-05	0.00540841	synonymous-codon, nc-transcript-variant	RNFT2	GRCh38.p7	12:116750126	TGGCGGCCACCGCGG[A/G]GGCTCCCTGCTGCAG	84900
rs781751136	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116820188	TCGACTTCCCTGGGC[C/T]CAGGTCATCCTCCTG	84900
rs781773996	in-del	-/GGT			intron-variant	RNFT2	GRCh38.p7	12:116743010	TGCTTGAGCCCAGGA[-/GGT]GGAGGTTGCAGTGAG	84900
rs796079797	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116741389	CAAAAATATCATAGA[A/G]TGGGTGGTTTAAACA	84900
rs796099588	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116760126	GGTTGTCAGGGAAGT[A/G]GGGGAAAGCTGGCAG	84900
rs796108681	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116843709	CAGCTGGGCCCTGGG[-/G]TAAACCTGGTTTTTT	84900
rs796142751	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116828993	TCTCTAAAACACACA[A/G]TGTTTTAAGTGGAAA	84900
rs796143925	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116818158	CCCCTCTCTACAAAA[A/G]AAGTCTTTAAAAAAT	84900
rs796193622	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116800634	GCAAGACTCTGTCTC[-/AA]AAAAAAAAAATGGTT	84900
rs796204279	in-del	-/AGGAAGGTA			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737542	AGGAGGAGGAAGGTG[-/AGGAAGGTA]AGGAAGGAAGGGAGG	84900
rs796267292	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116772103	TCTCAGATTTTTTTT[-/T]ATTTTGGAGACACAG	84900
rs796280736	in-del	A/CG			intron-variant	RNFT2	GRCh38.p7	12:116743246	AAAAAAAAAAAAACC[A/CG]TTAAAAAACACTCAT	84900
rs796356272	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116751209	GTATGAGCCACTGCC[C/T]CGGCCTACTATATTT	84900
rs796356587	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116825983	TTCATCTTGATACAG[-/A]AAAAAAAAAGGTTTC	84900
rs796363151	multinucleotide-polymorphism	CC/TT			intron-variant	RNFT2	GRCh38.p7	12:116849848	TTCCTTCCTTCCTTT[CC/TT]TTTTTTTTTTTAAAA	84900
rs796371299	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116774240	ATGATTATGCAACAA[C/T]GTGAATGTACTTAGC	84900
rs796390668	in-del	-/C			intron-variant	RNFT2	GRCh38.p7	12:116753153	TTTCTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	84900
rs796433098	in-del	-/AAAAT			intron-variant	RNFT2	GRCh38.p7	12:116790964	AGACCCTGTCTGAAA[-/AAAAT]AAAATAAAACAATAA	84900
rs796440574	in-del	-/AA			intron-variant	RNFT2	GRCh38.p7	12:116762065	GAGTGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAC	84900
rs796488941	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794107	CTGTCTCTATAAAAA[A/G]CTAAAAACGTATCCA	84900
rs796512848	in-del	-/A			intron-variant	RNFT2	GRCh38.p7	12:116749287	CCTCTTTCCCCCCCC[-/A]ACCACCCCTTTTGAG	84900
rs796520857	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116747230	CTGGCTACTTTTTAA[-/T]TTTTTTGTAGAGACA	84900
rs796543460	in-del	AG/GAGGAAGGTAA			upstream-variant-2KB, intron-variant	RNFT2, C12orf49	GRCh38.p7	12:116737541	AGGAGGAGGAAGGTG[AG/GAGGAAGGTAA]GAAGGAAGGGAGGCA	84900
rs796545112	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116831940	TTGAGACCAGCCTGG[A/G]CAACATGGTGAAATC	84900
rs796599399	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116772769	ACATGCCATTTTACA[A/G]CTCTTTCATTTACCA	84900
rs796600320	in-del	-/TTTGTTTG			intron-variant	RNFT2	GRCh38.p7	12:116801805	TTCTGTGGGGTTTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT	84900
rs796632031	in-del	-/TG			intron-variant	RNFT2	GRCh38.p7	12:116840923	TTAGGGGTATGTGTC[-/TG]TGTGTGTGTGTGTGT	84900
rs796641383	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116819218	GGGTGAAATGTCCAA[A/G]TAAGAGAGCGGGGAG	84900
rs796677794	snp	A/G			intron-variant	RNFT2	GRCh38.p7	12:116794668	AGGAAGGAAGGGAGG[A/G]AGGAAGGGAGGGAGG	84900
rs796726163	in-del	-/TATT			intron-variant	RNFT2	GRCh38.p7	12:116750829	TATATTATATATATA[-/TATT]ATATATATATTATAT	84900
rs796752640	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116756504	CTAAGGTATGTCCCT[C/T]GTATGCCATTTTGCT	84900
rs796759021	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116770403	TTGTGTAAGTCAACT[C/T]TGTGGTGTTCACACA	84900
rs796763608	in-del	-/ATTACACTA			intron-variant	RNFT2	GRCh38.p7	12:116756483	TCATAGATGGCTTTT[-/ATTACACTA]AGGTATGTCCCTTGT	84900
rs796778315	in-del	-/GGCCACATGTGGCTCT			intron-variant	RNFT2	GRCh38.p7	12:116795495	AATATAGTAGCTACA[-/GGCCACATGTGGCTCT]CTAAATTTAAATTAA	84900
rs796808893	in-del	-/G			intron-variant	RNFT2	GRCh38.p7	12:116763802	AAGGGGGCGGGGGGG[-/G]AAAGAACTAAAAGTA	84900
rs796829819	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116753148	TTCTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	84900
rs796909919	in-del	-/CT			intron-variant	RNFT2	GRCh38.p7	12:116826055	GATACTTGATTATGC[-/CT]CTCCTCCCTTCCTCC	84900
rs796938908	in-del	-/AAAAAAAAT			intron-variant	RNFT2	GRCh38.p7	12:116806375	ACTGTCTCAAAAAAA[-/AAAAAAAAT]ATATATATATATATA	84900
rs796968100	snp	C/T			intron-variant	RNFT2	GRCh38.p7	12:116827775	CTTGTTCTAGAGCTG[C/T]CCAATAGCAAGTGGG	84900
rs796983507	in-del	-/T			intron-variant	RNFT2	GRCh38.p7	12:116809848	AGCTAATTTTTTGTA[-/T]TTTTTTAGTAAAGAC	84900
rs796996479	snp	A/G			intron-variant, upstream-variant-2KB	RNFT2, C12orf49	GRCh38.p7	12:116739216	CAAGAAGATATTCAC[A/G]GAGGCTAAACCTTTT	84900
rs797018443	in-del	-/ATA			intron-variant	RNFT2	GRCh38.p7	12:116750889	ATATATATTATATAT[-/ATA]ATATATATATATATA	84900

Page 1 | 2