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

PAAF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs11217	snp	C/T	0.0154538	0.0865337	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876788	GAGGGCCCGAACGCA[C/T]GCTCCTACGCGGCGG	80227
rs635962	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73917824	tgcagtgagccgaga[A/C]catgccactgtgctc	80227
rs825863	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917618	ggctcacgcctgtaa[C/T]cccagcactttggaa	80227
rs825864	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917632	accccagcactttgg[A/G]aggccgaggcaggca	80227
rs935985	snp	C/T	0.372181	0.21811	intron-variant	PAAF1	GRCh38.p7	11:73927261	CAAGAATTCACAGTT[C/T]AAAGGAAGCCTGGGA	80227
rs935986	snp	A/T	0.482394	0.0921585	intron-variant	PAAF1	GRCh38.p7	11:73920227	tttaaattaaaaaaa[A/T]atataaaaaatatta	80227
rs935987	snp	C/T	0.0663309	0.169604	intron-variant	PAAF1	GRCh38.p7	11:73920105	aatgttatcacctta[C/T]atttgtcaaaactaa	80227
rs935988	snp	A/C	0.441841	0.160303	intron-variant	PAAF1	GRCh38.p7	11:73919884	TAAGTGAAGCAGTAT[A/C]CTTTCCTAACTGTTT	80227
rs935989	snp	G/T	0.0872718	0.189788	intron-variant	PAAF1	GRCh38.p7	11:73914117	TTTGGATTTACTGAG[G/T]TATCTTTTACATATG	80227
rs1122373	snp	A/G	0.28052	0.24813	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877195	CGAGGGATATGGAGG[A/G]AACAGGGTCCGGAAA	80227
rs1132819	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880566	GTGGTGGGCCCCTGT[A/G]GTCCCAGCTACTCGG	80227
rs1132820	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880576	cctgtagtcccagct[A/G]ctcgggagcctgagg	80227
rs1466218	snp	A/C	0.127254	0.217792	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878139	TAGTCTGTATTTTAG[A/C]CCACCTAAATTAAGT	80227
rs1531001	snp	A/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73895918	tcaagaccaccctgg[A/G]caacatagggggacc	80227
rs1598044	snp	A/G	0.122758	0.215196	intron-variant	PAAF1	GRCh38.p7	11:73920523	ATTATTTTTGAGACA[A/G]AGTCTCGCTTTGTCA	80227
rs1618529	snp	C/T	0.122411	0.214991	intron-variant	PAAF1	GRCh38.p7	11:73921649	GGACAGTGAAAGGAG[C/T]ACGGGCAGCCACCAT	80227
rs1630713	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883894	gatgaatggataaac[A/C]aaatgtagtatatcc	80227
rs1630767	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883874	gtagtatatccatac[A/C]acagagtattaccgg	80227
rs1631659	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73883748	ggatcacttgaggcc[A/C]agagttcaagaccag	80227
rs1670539	snp	C/T	0.450609	0.149185	intron-variant	PAAF1	GRCh38.p7	11:73926696	tttgagacagactct[C/T]gctccgtcgctcagg	80227
rs1670543	snp	C/T	0.494057	0.0541878	intron-variant	PAAF1	GRCh38.p7	11:73879265	GACAACAAATGTACT[C/T]AGCTTGGTTTTGGAC	80227
rs1670545	snp	C/G	0.494315	0.0530107	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875067	TATGCTACAGCCACA[C/G]TGAACTCTTTCCATC	80227
rs1670550	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73902934	tcaaactcctgacct[A/T]gtgatcgcctgccgt	80227
rs1670551	snp	A/G	0.498547	0.0269177	intron-variant	PAAF1	GRCh38.p7	11:73904682	AATTTTCCCATATAC[A/G]CATGTATGTATATTG	80227
rs1670552	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904946	AGACTTGTATCTATT[G/T]GGTTTGATATCTAAA	80227
rs1670553	snp	A/G	0.122758	0.215196	intron-variant	PAAF1	GRCh38.p7	11:73913761	ctaaagaaatatttg[A/G]tgagtaaatgaatAA	80227
rs1670558	snp	G/T	0.496778	0.0400063	intron-variant	PAAF1	GRCh38.p7	11:73899065	TTATAAACTTCCCTT[G/T]TTTCACTCTTCCAAG	80227
rs1670560	snp	A/G	0.0875959	0.190066	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889122	CTACGTTTTTCCCAG[A/G]TGTTTTGGCACAGCC	80227
rs1670561	snp	A/G	0.127944	0.218179	intron-variant	PAAF1	GRCh38.p7	11:73890114	AGTACTACTGCAGAA[A/G]AGATAAAAGGTTAGG	80227
rs1792154	snp	G/T	0.498481	0.027514	intron-variant	PAAF1	GRCh38.p7	11:73910360	TGAACAGACAGTAAT[G/T]GTAAGGATAGGACAA	80227
rs1792162	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73883853	tacttcgttcctttt[G/T]gtggcccggtaatac	80227
rs1792169	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73925667	CAAATAGAGAAAAAC[A/C]AAAGGGGAATATTTA	80227
rs1792170	snp	G/T	0.50375	0.0473547	intron-variant	PAAF1	GRCh38.p7	11:73902812	AGCAATTCTCCTGCC[G/T]CAGCCTCCCCAGTAA	80227
rs1792171	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904696	CGCATGTATGTATAT[G/T]GCTCCCTAGCAACAT	80227
rs1792172	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904785	GGGGAATATGAAATT[G/T]GCTTTATTTCTTACA	80227
rs1792173	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904951	TGTATCTATTGGGTT[G/T]GATATCTAAAGCCTT	80227
rs1792188	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73920015	ctttccttaacatcc[G/T]ggatccaatccagaa	80227
rs1792197	snp	A/G	0.127254	0.217792	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874815	GGATGATGAAACCCC[A/G]TCTCTACTAAAAATA	80227
rs1792198	snp	A/G	0.49655	0.04139	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875505	CCACAGTGGAGGGAT[A/G]CCTAATCCAGACAAG	80227
rs1792199	snp	A/G	0.496714	0.0404017	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877525	CTGTGTCCAGGCCCC[A/G]TACTGGATGCTTGGT	80227
rs1792201	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73907225	AATCGATAGGCATTT[G/T]GGACATTATAACACT	80227
rs1792202	snp	A/G	0.123105	0.215401	intron-variant	PAAF1	GRCh38.p7	11:73907399	CACACTGCAGACAGG[A/G]GAGGTGGAAGTTCAG	80227
rs1792203	snp	A/G	0.408359	0.193449	intron-variant	PAAF1	GRCh38.p7	11:73908401	tgtatatatatatgt[A/G]tatatatatgtgtgt	80227
rs2010583	snp	C/G	0.280256	0.248162	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876952	CCCACCTCTGTCCTC[C/G]CCGCACGCTTCTCGG	80227
rs2060964	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73889645	AAGAAATGAAGTCTT[C/T]TGAGAGCAAATCCAA	80227
rs2067912	snp	C/G	0.156407	0.23182	missense, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900304	TGTTTGATGTGAATT[C/G]TTGCAGGTTTTTCCC	80227
rs2067913	snp	C/G	0.343219	0.23197	intron-variant	PAAF1	GRCh38.p7	11:73900433	GAGGTATGAAGTGTG[C/G]TTTCTCCAAAAGGCT	80227
rs2444601	snp	A/G	0.491987	0.0627894	intron-variant	PAAF1	GRCh38.p7	11:73899971	CACAGCCATCTCTAG[A/G]TCTAGTTAAAGAGCT	80227
rs2511260	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887139	ttataaattacccag[C/T]ctcaggtattccttt	80227
rs2511274	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73907082	TGTGTATTTTTTCTC[C/T]TTTTTTTTTTCCATT	80227
rs2515095	snp	A/G	0.123105	0.215401	intron-variant	PAAF1	GRCh38.p7	11:73907142	CCTAGCCTCAGGAAT[A/G]CACAGCATAAAAAAA	80227
rs2886812	snp	G/T	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73894114	GGCCTTTATACATCA[G/T]TTTTTATTATTTTCT	80227
rs3018335	snp	C/T	0.494272	0.053207	intron-variant	PAAF1	GRCh38.p7	11:73897966	CTGGCGGATCACTCA[C/T]GGTTAGGAGCTGCAG	80227
rs3019137	snp	A/T	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73894592	acgtgcacaatgtgc[A/T]ggttagttacatatg	80227
rs3076363	in-del	-/AGAG	0.123452	0.215605	intron-variant	PAAF1	GRCh38.p7	11:73901087	TGTGTGCTGGGAAAT[-/AGAG]AGAGAGAGTGAGAGA	80227
rs3211440	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73921405	AAATTTCTAACATTC[A/C]AAAAAAAAAAAGTAC	80227
rs3741138	snp	C/G	0.194819	0.243834	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909492	AGGACTCCCAAGCAG[C/G]CTGAGCGCCCACAAT	80227
rs3741139	snp	C/T	0.258288	0.249863	intron-variant	PAAF1	GRCh38.p7	11:73900475	TTTCTACCTTTTCAG[C/T]GATTCATTTCTGGGG	80227
rs3758930	snp	A/C	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73879119	TTCAACTGGGACTTT[A/C]Ttgatgataatttct	80227
rs3758932	snp	A/G	0.171704	0.237423	intron-variant	PAAF1	GRCh38.p7	11:73879608	CAGTGGCTCACACCT[A/G]TAATCCTAGCACTTT	80227
rs3758933	snp	A/G	0.171704	0.237423	intron-variant	PAAF1	GRCh38.p7	11:73879689	TGGGCAACAAAGTGA[A/G]ACCCCCTCCCCATCT	80227
rs3926010	snp	C/T	0.388587	0.208071	intron-variant	PAAF1	GRCh38.p7	11:73926350	agcactttgggaggc[C/T]gaggcaggcctcagt	80227
rs4362170	snp	G/T	0.494272	0.053207	intron-variant	PAAF1	GRCh38.p7	11:73894364	AACAAAATAGGCTGG[G/T]TGTAGTGGCTCACAC	80227
rs4944035	snp	A/G	0.0126979	0.078662	intron-variant	PAAF1	GRCh38.p7	11:73922602	gcgggcggatcacga[A/G]gtcaggagatcgaga	80227
rs5792635	in-del	-/T	0.49703	0.0384237	intron-variant	PAAF1	GRCh38.p7	11:73896307	TTTCTTTTTTATTTA[-/T]TTTTTTTTTTATTGA	80227
rs5792636	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73900982	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs6592541	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73909331	GTCATTTATGCAGCT[C/T]CATCTTCTCTGCCCT	80227
rs7102066	snp	A/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73902443	AGTGCAAGCTTCACC[A/T]CCGATCTGGCCATCC	80227
rs7105293	snp	A/G	0.496746	0.040204	intron-variant	PAAF1	GRCh38.p7	11:73881150	TAATAAACTGTAACC[A/G]AAAGGCACAGTTTCT	80227
rs7107228	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73913166	acaggcgtgagccac[C/T]gcacctggcctgact	80227
rs7114340	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73927142	AACAATTTTTGTAAG[C/T]ACATAATTATGGATG	80227
rs7115579	snp	A/G	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73915565	gtgagccaagattgc[A/G]ccactgtactccagc	80227
rs7119270	snp	A/G	0.0228947	0.104514	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888502	TGACTGCTGCAGTTA[A/G]TATGCTCTGGTGAGA	80227
rs7119602	snp	C/G	0.27278	0.24896	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888755	GTATTATAGGTATCA[C/G]AAGATCTAAGTCTTA	80227
rs7122397	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73904717	CTAGCAACATTAAAA[C/T]AGCTTAATATGATAG	80227
rs7123227	snp	A/G	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73922901	AGTGAGGAGATTTAA[A/G]TTGCCAGATGAAACA	80227
rs7123871	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73922644	aacatggtgaaaccc[C/T]gtctctactaaaaat	80227
rs7926863	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73906986	CATAGGGTTGCACTA[C/T]CTCTCTACTCCATAC	80227
rs7927396	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73900839	tacaaaaaattagcc[A/G]ggcgtagtggcgggc	80227
rs7934784	snp	C/T	0.4941	0.0539917	intron-variant	PAAF1	GRCh38.p7	11:73892752	gcaagctccacctcc[C/T]gggttcacaccattc	80227
rs7937252	snp	A/G	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73911877	ggcctcaagtgatcc[A/G]ccctcctaagcctcc	80227
rs7940614	snp	A/G	0.0707826	0.174302	intron-variant	PAAF1	GRCh38.p7	11:73912298	ttcgatgtctaataa[A/G]taagttgaacttacc	80227
rs7942963	snp	A/G	0.166506	0.235645	intron-variant	PAAF1	GRCh38.p7	11:73904554	AGTATCAGCACTTGC[A/G]CCATTATTTTCCAAG	80227
rs7944702	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73892729	cagtggtgcagtctc[A/G]gctcactgcaagctc	80227
rs9651759	snp	A/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73891905	GGAATAATTTTCAAA[A/G]GTCTTTGTGATATAA	80227
rs9705041	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894301	tgagcccaggagttt[A/G]agaccagcctaggca	80227
rs9705042	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894303	agcccaggagtttga[A/G]accagcctaggcaac	80227
rs9734960	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880688	caagactctgtctcg[A/G]aaaaaaaaaaaaaaa	80227
rs10128615	snp	C/T	0.372592	0.217879	intron-variant	PAAF1	GRCh38.p7	11:73926115	TTTCTTTCTTTCTTT[C/T]TTTTTTTTGAGATGG	80227
rs10543174	in-del	-/TA	0.103438	0.202533	intron-variant	PAAF1	GRCh38.p7	11:73908286	ATATGTGTATATATG[-/TA]TATATATGTGTGTAT	80227
rs10590637	in-del	-/TG	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73892695	GATGGAGTCTCGCTC[-/TG]TTGCCCAGGCTGGAG	80227
rs10656357	in-del	-/TAATT	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73904742	GATAGAGAAACTAAA[-/TAATT]TAAATACACTTGTTA	80227
rs10793067	snp	A/G	0.498547	0.0269177	intron-variant	PAAF1	GRCh38.p7	11:73918424	GATCACTATTATAAA[A/G]TCACACTTACATATA	80227
rs10898950	snp	A/G	0.455383	0.142541	intron-variant	PAAF1	GRCh38.p7	11:73889843	GCAAAAACTCATTTA[A/G]TGAAAGGCCTGCAGG	80227
rs10898952	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73918251	AAAACAGGAGCTGCT[C/T]TGACCTTACCTGCCA	80227
rs11235937	snp	C/T	0.298398	0.245271	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875484	TACAGATAGCAAAGA[C/T]TGGGACCACAGTGGA	80227
rs11235938	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879543	TATCTTTCATTTCAA[A/G]TGCTGCTGATATATT	80227
rs11235939	snp	A/G	0.209997	0.246779	intron-variant	PAAF1	GRCh38.p7	11:73892174	CAGAAAAATACAAAA[A/G]TTAGCCAGACATGGT	80227
rs11235940	snp	C/T	0.190205	0.242744	intron-variant	PAAF1	GRCh38.p7	11:73893315	CTCTGTAAAACATAC[C/T]GTTAGGTTGAAAGTT	80227
rs11235941	snp	A/G	0.190205	0.242744	intron-variant	PAAF1	GRCh38.p7	11:73894018	ctgttgcccaggctg[A/G]tctcaaactcctgac	80227
rs11235942	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73894658	ATCTACTAAAAAAAA[A/T]AAAAATAAAAAAAAA	80227
rs11235943	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73894665	AAAAAAAATAAAAAT[A/T]AAAAAAAAATCAGCT	80227
rs11235944	snp	A/G	0.25912	0.249834	intron-variant	PAAF1	GRCh38.p7	11:73896227	TAGCTATACCTATAT[A/G]TAGGTATATGTGGAA	80227
rs11235945	snp	C/T	0.203267	0.245593	intron-variant	PAAF1	GRCh38.p7	11:73896567	CGCCCTTAATCCATT[C/T]AACCCTGAGTGGATA	80227
rs11235946	snp	C/T	0.209693	0.246729	intron-variant	PAAF1	GRCh38.p7	11:73896581	TCAACCCTGAGTGGA[C/T]ACAGCACATGTTTCA	80227
rs11235947	snp	A/G	0.203267	0.245593	intron-variant	PAAF1	GRCh38.p7	11:73896605	TGTTTCAGAGAGCAC[A/G]GGGTTGGGGGTAAGG	80227
rs11235948	snp	C/T	0.213937	0.247385	intron-variant	PAAF1	GRCh38.p7	11:73915910	CATTTTTGCTAATAT[C/T]GCCTTTGTACTTGAG	80227
rs11235949	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918361	TACTTAATTTTTTTT[C/T]TTTTTTTTTTTTTTT	80227
rs11235950	snp	A/G	0.165527	0.235296	intron-variant	PAAF1	GRCh38.p7	11:73922577	AATCCCAGCACTTTC[A/G]GAGGCCGAGGCGGGC	80227
rs11235951	snp	C/T	0.170084	0.236883	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927813	CTTCCTCAGCACTCC[C/T]TGTTGCCTGGCCATA	80227
rs11235952	snp	A/C	0	0	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927940	GAACTAAGGGGTTTT[A/C]TGTGACTTGAAACTT	80227
rs11367834	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73922835	AAAAAAAAAAAAAAA[-/A]GAAGTTGGATATAGA	80227
rs11460827	in-del	-/T	0.38821	0.208322	intron-variant	PAAF1	GRCh38.p7	11:73902655	CTAAGAATATGTATG[-/T]GACCTTTAGCTTAGA	80227
rs11603390	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73916767	CTATTGAATCAAGGG[G/T]ATATTTTTCCATTTA	80227
rs11606863	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73894926	gaggtcagggctgca[C/G]tgagctgtgattgtg	80227
rs11821823	snp	C/G	0.0528381	0.153711	intron-variant	PAAF1	GRCh38.p7	11:73882960	gctggagtacagttg[C/G]atgattatggcttac	80227
rs12270286	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880413	TTCAAAAATCCTATT[C/T]TAACTGCTtgagcta	80227
rs12270333	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880476	AGAGCAAAACCCTGT[C/T]TCAGTTAAAAAAAAA	80227
rs12275878	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73918269	ACCTTACCTGCCATT[C/T]TAAGTTTATTCCAAG	80227
rs12280978	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896287	gatgtttcttttttt[C/T]tttttttctttttta	80227
rs12280981	snp	C/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73896295	tttttttcttttttt[C/T]ttttttatttatttt	80227
rs12281606	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886634	gctgagatcacgcca[C/T]tgcactccagcctgg	80227
rs12284235	snp	C/T	0.361684	0.223667	intron-variant	PAAF1	GRCh38.p7	11:73903364	CAACCTATAGATTGA[C/T]CGATCATCACTGTCT	80227
rs12287867	snp	C/T	0.00597247	0.0543191	intron-variant	PAAF1	GRCh38.p7	11:73905230	TGAAATTGCTGCttt[C/T]tttttttttttgaga	80227
rs12289171	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896286	cgatgtttctttttt[C/T]ctttttttctttttt	80227
rs12289172	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896294	ctttttttctttttt[C/T]cttttttatttattt	80227
rs12290910	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73927206	TCCATGGGACTAGTG[C/T]GTGTCAATCATAAGC	80227
rs12293218	snp	C/T	0.0444908	0.142359	intron-variant	PAAF1	GRCh38.p7	11:73898836	aaacaaacaaacaaa[C/T]aaataaaTGCAACAC	80227
rs12295206	snp	C/T	0.188	0.24219	intron-variant	PAAF1	GRCh38.p7	11:73889306	AGTCACTTTGCTAAT[C/T]TGATATTGCTACATT	80227
rs12362085	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894022	tgcccaggctggtct[C/T]aaactcctgacttca	80227
rs12363553	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894023	gcccaggctggtctc[A/G]aactcctgacttcaa	80227
rs12363562	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894066	ccttggcttcccaaa[A/G]tgctgggattatagg	80227
rs12366026	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901967	atcccaggctcatgc[A/G]atccttgtgcctcag	80227
rs12366229	snp	A/G	0.207253	0.246318	intron-variant	PAAF1	GRCh38.p7	11:73897911	gagcactgagtgaac[A/G]agactccgtctgcaa	80227
rs12576689	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73910203	gctgggactacaggc[C/T]tgcaccaccatgcct	80227
rs12786003	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73914134	ATCTTTTACATATGG[G/T]AAAAGTCACCCTTTT	80227
rs12786118	snp	A/G	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73880558	cggatgtggtggtgg[A/G]cccctgtagtcccag	80227
rs12787838	snp	C/G/T	0.0950157	0.199331	intron-variant	PAAF1	GRCh38.p7	11:73880649	accagatagtgccac[C/G/T]gcattccagcttgga	80227
rs12790445	snp	C/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73920008	agtggtattctggat[C/T]ggatccaggatgtta	80227
rs12791050	snp	A/G	0.118235	0.212457	intron-variant	PAAF1	GRCh38.p7	11:73898687	ggcacagtggtgtgc[A/G]cctgtagtcccagct	80227
rs12792711	snp	A/G	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73898454	ctcctgggctcaagt[A/G]atcttcctgccttgg	80227
rs12793555	snp	C/T	0.101301	0.200969	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888449	GATGGGTAAGCAAAG[C/T]GTTGGAGAACCCATG	80227
rs12793757	snp	C/T	0.100944	0.200705	intron-variant	PAAF1	GRCh38.p7	11:73880748	tcacgcctgtgatcc[C/T]agcactttaggaggc	80227
rs12793826	snp	C/G	0.100944	0.200705	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876114	cctgggttacagcgg[C/G]agaccctgtctcaaa	80227
rs12795932	snp	G/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73903445	TCTTGGTccgggcac[G/T]gtggctcatgcctgt	80227
rs12796341	snp	C/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73885016	aggcgcccgccacta[C/T]gcccggctaattttt	80227
rs12799686	snp	A/G	0.100944	0.200705	intron-variant	PAAF1	GRCh38.p7	11:73913843	cagtattgtatccca[A/G]ctcctagtgtggtgt	80227
rs12799745	snp	G/T	0.120674	0.21395	intron-variant	PAAF1	GRCh38.p7	11:73881270	TAATATTTTGCATTT[G/T]TCTTGCCGATACATA	80227
rs12801553	snp	A/G	0.100944	0.200705	intron-variant	PAAF1	GRCh38.p7	11:73882345	GAAGGTAACTTGTAG[A/G]TTCAGTTTTCTTTAT	80227
rs12802435	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917716	gtctctactaaaaat[A/G]caaaaattagctggg	80227
rs12802436	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917718	ctctactaaaaatac[A/G]aaaattagctgggca	80227
rs12803118	snp	A/G	0.101658	0.201233	intron-variant	PAAF1	GRCh38.p7	11:73896382	aggacaatagtggag[A/G]gaaggtcagcagata	80227
rs12804029	snp	C/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73914081	aaGTACACACACACA[C/T]AGGCACATTTTAAAA	80227
rs12807844	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896288	atgtttctttttttc[C/T]ttttttcttttttat	80227
rs12807851	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896296	ttttttctttttttc[C/T]tttttatttattttt	80227
rs12808007	snp	C/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73883675	gcgcctgccaccaca[C/T]ccgggtaatttttgt	80227
rs17132438	snp	C/T	0.0535932	0.154675	intron-variant	PAAF1	GRCh38.p7	11:73879458	TTTTCAAATTGTAAC[C/T]GAGGTGGTACCATTC	80227
rs17132488	snp	A/G	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73917011	AGATTGAAAGATTGA[A/G]TTATTTTTATTTATT	80227
rs17132495	snp	C/T	0.388398	0.208197	intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919292	CACCACTCTTCTGCC[C/T]TAAAGGAGCTCACAG	80227
rs17244692	snp	A/G	0.117886	0.21224	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887241	ACCTGTTTTTCTTTC[A/G]TGGGCCAATTTCATG	80227
rs17850051	snp	C/T	1.65034e-05	0.00287253	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887423	TCCCAGAGGTTACAG[C/T]TTCAGAAGGATTTAC	80227
rs28420543	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73900964	TCCAACCTGGGCGAC[A/C]GAGCGAGACTCCGTC	80227
rs28472323	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908415	TGTATATATATGTGT[A/G]TATATATATATATGG	80227
rs28495881	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908421	TATATGTGTGTATAT[A/G]TATATATGGGTCTTG	80227
rs28639780	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908413	TGTGTATATATATGT[A/G]TGTATATATATATAT	80227
rs28729523	snp	A/G	0.0663309	0.169604	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924847	TGGCAAGAAATCAAG[A/G]GCTTAACTCAGAAGT	80227
rs34028528	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73880579	TAGTCCCAGCTACTC[-/G]GGGAGCCTGAGGCAG	80227
rs34083941	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73879873	TGAGACCCCATCATT[-/A]AAAAAAAAAAAGACT	80227
rs34202768	snp	C/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73900778	ACGAGGTCAGGAGAT[C/G]GAGACCATCCCGGCT	80227
rs34217459	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73905225	ATTCTTGAAATTGCT[A/G]CTTTCTTTTTTTTTT	80227
rs34242715	in-del	-/T	0.158302	0.232576	intron-variant	PAAF1	GRCh38.p7	11:73882312	GCACCGTGCCTGCAC[-/T]TTTTTTTTTTTTTTT	80227
rs34255455	in-del	-/G	0.497329	0.0364438	intron-variant	PAAF1	GRCh38.p7	11:73897885	ACTGCACTCCAGCCT[-/G]GGGCACCATTGAGCA	80227
rs34258880	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73901571	TTGTGAACCTCAGTA[C/T]ATTGTAACTTGTGTG	80227
rs34308910	snp	A/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73891646	TGAGCGTGGTGGCAC[A/T]TACCTGTAGTCCTAG	80227
rs34408148	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73900705	AGTTGTTTTCTGGCC[-/G]GGCGCGGTGGCTCAC	80227
rs34408861	in-del	-/A			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925175	AAAAAAAAAAAAAAA[-/A]CAAGTGACTTCTGGC	80227
rs34481167	snp	A/C	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73897729	AGGGGCTCCTCACAT[A/C]CCAGAAGATGGGCGG	80227
rs34540814	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73894770	AGAGGTTGCAGTGAG[-/C]CCGAGGTTGCGCCAC	80227
rs34551219	in-del	-/A	0.391024	0.206427	intron-variant	PAAF1	GRCh38.p7	11:73903717	TGAAACTCTGTCTTC[-/A]AAAAAAAAAAAAATC	80227
rs34558585	in-del	-/A	0	0	intron-variant	PAAF1	GRCh38.p7	11:73880483	AACCCTGTCTCAGTT[-/A]AAAAAAAAAAAAAAA	80227
rs34578576	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73923255	AAATTTGGAAAACAG[C/T]TGTTCAGATTTCCAA	80227
rs34598736	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73921394	TTCTACTTTTTGTAC[-/T]TTTTTTTTTTGGAAT	80227
rs34616917	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73884264	AGCACTTTGGGAGGC[-/T]TGAGGCAGAAGGATT	80227
rs34659829	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73922264	TTCTGCTGGGAAGAA[A/G]GCAAGGCATAACTTC	80227
rs34895752	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73901566	TGTTTTTGTGAACCT[C/T]AGTACATTGTAACTT	80227
rs34941273	in-del	-/TGT	0.155656	0.231515	intron-variant	PAAF1	GRCh38.p7	11:73881639	AAGCAACAAACTTAA[-/TGT]TGTTGTTGTTGTTGT	80227
rs34995720	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876635	TGGCAGCCACGAGGC[A/C]TGAGGCGCCTCAGGC	80227
rs35017347	in-del	-/TCTC	0.22263	0.248497	intron-variant	PAAF1	GRCh38.p7	11:73926021	ACGTAATTGAGACTA[-/TCTC]TATATATTGCCCTGT	80227
rs35018990	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73907349	ACTCCCCTGACACTA[-/C]CCTGGCAAAAGTGGA	80227
rs35066247	snp	C/T	0.103082	0.202275	intron-variant	PAAF1	GRCh38.p7	11:73894537	CCTAATGTTAAATGA[C/T]GAGTTAATGGGTGCA	80227
rs35121677	in-del	-/TG			intron-variant	PAAF1	GRCh38.p7	11:73908298	ATATATGTATATATA[-/TG]TGTGTATATATGTAT	80227
rs35123949	snp	A/C	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73912701	TGGCCTCCCTTTATA[A/C]ATATGTTGAAATCCT	80227
rs35133035	snp	C/T	0.131038	0.219882	intron-variant	PAAF1	GRCh38.p7	11:73893786	AACTAAACGTGGGCG[C/T]GGTGGCTCATGCTTA	80227
rs35208638	snp	G/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73890743	CTTTATGTCCTCTTC[G/T]CACTGATCCTGTTCC	80227
rs35218096	in-del	-/TT			intron-variant	PAAF1	GRCh38.p7	11:73901871	CCACTGCGCCTTGCC[-/TT]TTTTTTTTTTTTTTT	80227
rs35248853	snp	A/C	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73885979	CTGCTAGACTTAAGG[A/C]CTTCACAGTCTGTTG	80227
rs35338762	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73891852	TTTTCCTATAGGACA[-/G]GGGATATTTTCTCAA	80227
rs35344902	snp	C/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73893778	AAAGAAAAAACTAAA[C/T]GTGGGCGCGGTGGCT	80227
rs35383903	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73912971	AACCTCCACCTCCTA[-/G]GTTCAAGCAATTCTC	80227
rs35481171	snp	A/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73903239	CTTTCCAGTTCGTTG[A/T]ATAAAGTAGCCCCAG	80227
rs35489844	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73900709	TTTTCTGGCCGGGCG[-/C]CGGTGGCTCACGCCT	80227
rs35531604	snp	C/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73897938	GCAATCCCGGCACCT[C/T]GGGAGGCCGAGGCTG	80227
rs35598792	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73916750	GCCTAGCATATAGAT[A/G]ACTATTGAATCAAGG	80227
rs35623031	in-del	-/A	0.496778	0.0400063	intron-variant	PAAF1	GRCh38.p7	11:73921300	GTGAGACTGCCTCGC[-/A]AAAAAAAAAAAAAAT	80227
rs35681608	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73899067	GGAAGAGTGAAAAAA[-/G]GGGAAGTTTATAACA	80227
rs35741071	snp	G/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73902715	ATTATTATTTTTTTT[G/T]AGATGGAGTCTCACT	80227
rs35766780	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894158	GAGAAGGCAATTCAC[C/T]TCTTGGGAGAGTTGG	80227
rs35940075	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73923671	TCCTGAGTATCTGGG[-/G]ATTACAGGCATGCAC	80227
rs35976844	snp	A/G	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73895406	GATACCACCTGTATC[A/G]GGACAGAACCTGAAG	80227
rs36076594	snp	A/G	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73882634	TTGAGACGGAGTCTC[A/G]CTCTGTTGCCCAGGC	80227
rs36097357	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73895411	ACCTGTATCAGGACA[-/G]GAACCTGAAGTATGT	80227
rs55697916	in-del	-/AA	0	0	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886697	AAAAAAAAAAAAAAA[-/AA]GAAAATGTATTTTAG	80227
rs55818010	in-del	-/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73918362	CTTAATTTTTTTTTT[-/G]TTTTTTTTTTTTTTT	80227
rs55865006	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916971	GCTCAGTAATTTTCT[C/T]TTACATTAGACCCTG	80227
rs55886322	in-del	-/CCCC			intron-variant	PAAF1	GRCh38.p7	11:73879700	TGAGACCCCCTCCCC[-/CCCC]ATCTCTATAAAAAAC	80227
rs56032404	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73879696	CAAAGTGAGACCCCC[C/T]CCCCATCTCTATAAA	80227
rs56077210	in-del	-/AT	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73908293	TATATATGTATATAT[-/AT]GTGTGTATATATGTA	80227
rs56117405	snp	A/G	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73901476	CCTTCTTCTGGAACC[A/G]TAATACATATTGCGT	80227
rs56403663	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73879717	CTCTATAAAAAACAA[-/A]AAAAAATTAGTCAGG	80227
rs56957343	snp	C/T	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73926169	TGGAGTGCAATGGCG[C/T]GATCTCAGCCCACAG	80227
rs57462976	snp	C/G	0.0146691	0.0843764	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889027	GAGAGGTTAATTAAT[C/G]TCAAATAATCAAAGA	80227
rs57736748	snp	A/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73893166	GTTTTGCTCCCAAAG[A/T]TGGGAAGAAATTAGA	80227
rs57825029	in-del	-/A			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875681	CAAAAAAAAAAAAAA[-/A]GTTCAGTGATGGGAG	80227
rs58199491	snp	C/T	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73908809	TATTTATTTATTTTT[C/T]GAGACGGAGTCTCCT	80227
rs58589518	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887714	TTAAAATTTTCTAGT[C/G]GCCACATTATAGAGA	80227
rs58934862	in-del	-/AAAAAAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73880707	AAAAAAAAAAAAAAA[-/AAAAAAAAAAA]GCCAGGCACAGCAGC	80227
rs59496736	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926595	GTGTGTGTAGTCCCA[A/G]CTACTTGGGAGGCTG	80227
rs59668637	snp	C/T			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925078	GAGAATCGCTTGAAC[C/T]TGGGAGGTGGAGGCT	80227
rs59875647	snp	A/G	0.0422008	0.138995	intron-variant	PAAF1	GRCh38.p7	11:73895800	ATGCATGAAGTGATT[A/G]CTGATACTGAAATTA	80227
rs60093210	snp	A/G	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73902144	TGGGATTACAGGTAT[A/G]AGCCACTGCGCCTGG	80227
rs60469198	in-del	-/A			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876127	TCAAAAAAAAAAAAA[-/A]ARAAAAAAAAAAAGG	80227
rs60520592	snp	C/T	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73915530	GGAATATCACCTTAG[C/T]CTGGAAGGTCGAGGC	80227
rs60646364	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902300	CATTGAGAGGGAATA[A/G]AAACAATATTCAGAG	80227
rs60812833	snp	A/C	0.178785	0.239642	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925168	TCTCAAAAAAAAAAA[A/C]AAAAAAACAAGTGAC	80227
rs60863026	snp	A/G	0.178785	0.239642	intron-variant	PAAF1	GRCh38.p7	11:73922734	AGGCAGGAGAATGGC[A/G]TGAACCTGGGAAGTG	80227
rs60965741	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919098	TAAACATAGTTTTAA[A/G]TGTCTGATCTATGGC	80227
rs61109105	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73911173	TAGGGCTTACTCTTG[A/G]TGTTATATATCCTAT	80227
rs61247788	snp	C/T			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925123	GATCGTACCACTACA[C/T]TCCAGCCTGGGCAAC	80227
rs61429432	in-del	-/A/AA	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73913711	AAAGAAAAAAAAAAA[-/A/AA]GAAAAAAAGAATAGT	80227
rs61616797	snp	A/G	0.0532157	0.154195	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878685	AAGTACTATGACCAA[A/G]CTGGAGGTTACATGA	80227
rs61720052	in-del	-/AAAAAAAAAAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73901000	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAA]GTTGTTTTCTACAAT	80227
rs61901161	snp	A/G	0.110519	0.207473	intron-variant	PAAF1	GRCh38.p7	11:73895876	CTTTGGGAGGCCAAG[A/G]CAGAAGGATAGCTTG	80227
rs61901162	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73897175	CGGGGCGGCTGGCCG[G/T]GCGGGGGGCTGACCC	80227
rs61901163	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904552	GCAGTATCAGCACTT[G/T]CGCCATTATTTTCCA	80227
rs61901164	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73905843	AGAATTTTTTTTTTC[C/T]AAAAGCATGTATCAC	80227
rs61901165	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73907405	GCAGACAGGGGAGGT[A/G]GAAGTTCAGCTTCCC	80227
rs61901166	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915368	CCCAGCTTTCTGGGA[A/G]GCCCAGAAAGGGTGG	80227
rs66992843	in-del	A/GGG/GGGG/GGGGG/GGGGGG	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73879696	TTTATAGAGATGGGG[A/GGG/GGGG/GGGGG/GGGGGG]GGGGGTCTCACTTTG	80227
rs71065053	in-del	-/A	0	0	intron-variant	PAAF1	GRCh38.p7	11:73899431	CAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs71065054	in-del	-/TTAAA	0	0	intron-variant	PAAF1	GRCh38.p7	11:73904745	TCTTAACAAGTGTAT[-/TTAAA]TTATTTAGTTTCTCT	80227
rs71272248	in-del	-/A	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73896269	AAAAAGAAACATCGT[-/A]AAAAAAAAAAAAAAA	80227
rs71464087	snp	C/T	0.100588	0.200439	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877406	TTACTTCCAGAAGTC[C/T]CTGTACTCACCACCA	80227
rs71464088	snp	A/G	0.0704125	0.17392	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877612	ACATCCAGGCCAGGC[A/G]CAGTGGCTCATGCCT	80227
rs71464089	snp	G/T	0.100588	0.200439	intron-variant	PAAF1	GRCh38.p7	11:73882871	GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA	80227
rs71464090	snp	G/T	0.304688	0.243945	intron-variant	PAAF1	GRCh38.p7	11:73885746	ACTTGGGAGGCTGAG[G/T]CATGAGAACTGCTTG	80227
rs71464091	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73892114	GATCACTTGAGCTCA[A/G]GAGTTCAAGACCAGC	80227
rs71464094	snp	A/C	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73900871	CCTGTAGTCCCAGCT[A/C]CTTGGGAGGCTGAGG	80227
rs71464095	snp	A/G	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73914970	TCAATCTCCCAAAGT[A/G]CTGGGAGTACAGATG	80227
rs71464096	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73923417	AGGCACAAAAAAATA[A/G]ATCAAAATGTTAACA	80227
rs71467813	multinucleotide-polymorphism	ATACTA/GTACTG	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73901566	CACACAAGTTACAAT[ATACTA/GTACTG]AGGTTCACAAAAACA	80227
rs71469477	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73879878	CCCCATCATTAAAAA[-/A]AAAAAAGACTATTGT	80227
rs71469481	in-del	-/A	0.121022	0.21416	intron-variant	PAAF1	GRCh38.p7	11:73901198	ATCATCAGACATTAT[-/A]GATAGAGCTTGATGA	80227
rs72477726	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897306	CCCACTTCMCTCCCG[A/G]ACGAGGTGGCTGCCA	80227
rs72982931	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876142	AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAGGTA	80227
rs72982937	snp	A/G	0.209693	0.246729	intron-variant	PAAF1	GRCh38.p7	11:73885464	TTTTATTCTTGATAT[A/G]CTCCTCCTTGACTTG	80227
rs72982939	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73889997	GAAACCATTCTTTCT[A/G]ATGAACTGTGAGGAC	80227
rs72982946	snp	A/G	0.114387	0.210022	intron-variant	PAAF1	GRCh38.p7	11:73911448	TTAGCCTCCCAAAGT[A/G]CTAGGATTACAAGCA	80227
rs73541941	snp	A/G	0.031825	0.122064	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878257	CAGAAGGCTTAATTT[A/G]CCCAAGATCATGCAT	80227
rs73541950	snp	A/G	0.00277861	0.0371697	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887329	TTTCTTATTTTTTGA[A/G]ACATGCTTCTTTTGT	80227
rs73549951	snp	C/G	0.031825	0.122064	intron-variant	PAAF1	GRCh38.p7	11:73895761	TGCATGTGTATAAAA[C/G]ATTTGTTATTCTGAT	80227
rs73549968	snp	C/T	0.213937	0.247385	intron-variant	PAAF1	GRCh38.p7	11:73907479	GCACCACCTGACTTG[C/T]ATCACCTCATTGCCT	80227
rs73549971	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73907692	CTGCTGCCGGCTTCC[A/G]TGGGAGCGGGGTAGA	80227
rs73549976	snp	A/G	0.00133345	0.0257866	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909519	TCCTTGCAGATTGTG[A/G]TTCTTCTATCAATGG	80227
rs73549981	snp	A/G	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73913256	CTGTTCACCATTCAG[A/G]TCTTGCCATTCAGTT	80227
rs73549983	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915250	TGTAAAATGATGAAG[C/T]TGTATAGATTTTCTT	80227
rs73549988	snp	C/G	0.0119091	0.0762411	intron-variant	PAAF1	GRCh38.p7	11:73915947	TGCTGGCTTTTACTT[C/G]CAGAGGGAAATCAGG	80227
rs73549995	snp	A/C	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73922019	TTCATTCTTAACTTC[A/C]TAGTTTTTGAAGAAG	80227
rs74441746	snp	A/G	0.0535932	0.154675	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875632	TTTGGTCAATGGAAG[A/G]GCAGGTGGTTGAGAT	80227
rs74454343	snp	A/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73921314	CAAAAAAAAAAAAAA[A/T]TCTCTGTTGCAAGGT	80227
rs74703265	snp	A/G	0.0537601	0.154887	intron-variant	PAAF1	GRCh38.p7	11:73883387	TAACAGTCACTTTCC[A/G]CCCCCCAATCCTAGC	80227
rs74728570	snp	G/T	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73907666	CCCCACTGGGTAGGG[G/T]AATGGGAGTGCTGCT	80227
rs74818755	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73894642	TAATAATAAAAAAAA[-/A]ATCTACTAAAAAAAA	80227
rs74944195	snp	C/G	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73915165	TAGGGTATGTGATGA[C/G]GATTAAATGGTCTAC	80227
rs75053025	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73914714	TTTTTTTTTTTTTTT[G/T]TGGAGACAGAGTCTC	80227
rs75236868	snp	C/G	0.00993419	0.0697739	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888530	AGATGATTCCGTAAG[C/G]GTGGACCAGCCTTTT	80227
rs75270088	snp	A/C	0.00835141	0.0640778	intron-variant	PAAF1	GRCh38.p7	11:73902192	AATATTTCTTTATAA[A/C]ATTTTGCCAGATTAC	80227
rs75351017	snp	A/T	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73915302	GGTAATGTGAAAAAA[A/T]TCTGAGTAAAGAACT	80227
rs75865129	snp	C/T	0.0232847	0.105357	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927988	GCAGTCTCAAACCAA[C/T]ATGATTGGTCAGCCT	80227
rs76061368	snp	A/C	0.0134861	0.0810011	intron-variant	PAAF1	GRCh38.p7	11:73884065	AATTGGATTGGTGAC[A/C]GTCGGCACAGTTGTG	80227
rs76092645	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73896275	TTTTTTTTTTACGAT[G/T]TTTCTTTTTTTCTTT	80227
rs76103145	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73917886	AAAAAAAAAAAAAAA[A/G]AGATACAGACTCTGC	80227
rs76147299	snp	C/T	0.0225045	0.103662	intron-variant	PAAF1	GRCh38.p7	11:73884068	TGGATTGGTGACAGT[C/T]GGCACAGTTGTGTTC	80227
rs76201855	snp	A/T	0.0244538	0.107838	intron-variant	PAAF1	GRCh38.p7	11:73896310	CTTTTTTATTTATTT[A/T]TTTTTTTATTGATCA	80227
rs76288991	snp	C/T	0.105569	0.204058	intron-variant	PAAF1	GRCh38.p7	11:73880559	GGATGTGGTGGTGGG[C/T]CCCTGTAGTCCCAGC	80227
rs76332820	snp	G/T	0.0189856	0.0955633	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876808	CTACGCGGCGGCTTG[G/T]GTTTCGCAGGCGGTT	80227
rs76561387	snp	A/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73885822	ACTCCAGCCTGGGCG[A/T]CAAGAGTGAAACTCC	80227
rs76569027	snp	A/G	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73879401	TCCCAAGTCTTATCA[A/G]TTTTTCTTTTGAACA	80227
rs76577804	snp	A/G	0.0337553	0.125452	intron-variant	PAAF1	GRCh38.p7	11:73907425	TTCAGCTTCCCCCTT[A/G]GTCCTGTGTCATCTT	80227
rs76689874	snp	A/G	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73926800	ACTGGGGCCTGGGGG[A/G]TTGAGAAAGTTGCCC	80227
rs76708424	snp	C/T	0.0539704	0.155153	intron-variant	PAAF1	GRCh38.p7	11:73883705	TATTTTCAGTAGAGA[C/T]GAACGAGGTTTCGAC	80227
rs76714306	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73892327	GACACTGTCTCACCA[A/C]AAAAAAAAAAAAAAA	80227
rs76761901	snp	C/T	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73927043	AATGGGTTTGCTTTC[C/T]ACTTGGGCCAATTAG	80227
rs76764350	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877340	GGGATACTGGGAGGC[A/C]GGAAGGCTTTTGGCC	80227
rs76789439	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73896272	TTTTTTTTTTTTTAC[G/T]ATGTTTCTTTTTTTC	80227
rs76906369	in-del	-/TT	0.178144	0.239451	intron-variant	PAAF1	GRCh38.p7	11:73926112	TTCTTTCTTTCTTTC[-/TT]TCTTTTTTTTGAGAT	80227
rs77001985	snp	G/T	0.030665	0.119967	intron-variant	PAAF1	GRCh38.p7	11:73905607	TTCTTTATTCTTGTC[G/T]TGTAAGTGTTAAGAG	80227
rs77070819	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73911640	TTTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTCA	80227
rs77125132	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73916794	TTTACAAAGGTTTTC[C/T]AGTCTGAATTTTCTG	80227
rs77162976	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917922	AGGCACCTGGAGTCT[A/C]ATGGTAAAGATGGAC	80227
rs77242966	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73925545	CTCACTAGTCTGTCA[A/G]TTCATCTGTAAAGAT	80227
rs77291934	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883953	GGCTATTATGAAGGA[A/G]GGAGATTTTGATGGC	80227
rs77296683	snp	C/T	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73921908	TTCCCAGTGTATACA[C/T]TTCTTTCTCACCTTG	80227
rs77303137	snp	A/G	0.128632	0.218563	intron-variant	PAAF1	GRCh38.p7	11:73915334	ACGCCCACTGGGCAT[A/G]GTGGCTCATGCCTGT	80227
rs77487130	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876128	GGAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAGA	80227
rs77545317	snp	A/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73879874	TGAGACCCCATCATT[A/T]AAAAAAAAAAGACTA	80227
rs77546964	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73914715	TTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTCA	80227
rs77574810	snp	C/T	0.0115144	0.0749975	intron-variant	PAAF1	GRCh38.p7	11:73890878	CAGCTTATTTCAACA[C/T]AAAAAGATAATGGCA	80227
rs77966831	snp	C/T	0.0425829	0.139564	intron-variant	PAAF1	GRCh38.p7	11:73886093	TTAACTTCATTCTAT[C/T]ATCTGCGTGTGTTTA	80227
rs78002088	snp	C/T	0.210301	0.246828	intron-variant	PAAF1	GRCh38.p7	11:73880773	GGAGGCTGTGGCGGG[C/T]GGATCACCTGAGGTC	80227
rs78104990	snp	C/T	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73892392	TACAAAACAGATATA[C/T]ACTTAGTGATGAAAA	80227
rs78235624	snp	A/C	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73927163	ATTATGGATGTAATT[A/C]TGTTGCCTTCATAAA	80227
rs78236555	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73904851	TTCGTATTTCCAGAC[C/T]TTGGCTGGGATGCTC	80227
rs78430125	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73922819	GAGACTCCGTCTCAA[A/C]AAAAAAAAAAAAAAA	80227
rs78485569	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73925468	GAGACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAG	80227
rs78499538	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875800	GACTTTTTATTCTGA[A/G]GGCAATGGGGAATCA	80227
rs78664341	snp	A/C	0.0657548	0.168978	intron-variant	PAAF1	GRCh38.p7	11:73914524	GTGGTTCCTATATGA[A/C]CTTTGAACTCTGAGG	80227
rs78699899	snp	C/T	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888240	TTAGAAATACTTGAT[C/T]TGTATTTAGGTTTTA	80227
rs78767496	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73913701	TGAGGGTAAAAAAAG[A/G]AAAAAAAAAAGAAAA	80227
rs78860005	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900464	TCTCTAATGATCCCC[A/G]GAAATGAATCACTGA	80227
rs78960781	snp	A/G	0.046775	0.145601	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876890	ACACGGAAGGGGCGG[A/G]GAATGTGAAAAAGTC	80227
rs79033493	snp	A/T	0.0228947	0.104514	intron-variant	PAAF1	GRCh38.p7	11:73923022	ACTTAAGCTATTATC[A/T]ATATATTGCTAATCT	80227
rs79064888	snp	A/T	0.0283406	0.115616	intron-variant	PAAF1	GRCh38.p7	11:73879107	CACTTCTGCAGCTTC[A/T]ACTGGGACTTTCTTG	80227
rs79192423	snp	G/T	0	0	splice-acceptor-variant	PAAF1	GRCh38.p7	11:73924614	TCTTTCTGCCTTTCA[G/T]GTGATGGAAGCTGTT	80227
rs79305023	snp	C/T	0.0528381	0.153711	intron-variant	PAAF1	GRCh38.p7	11:73880481	AAAACCCTGTCTCAG[C/T]TAAAAAAAAAAAAAA	80227
rs79386318	snp	G/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73914717	TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTCACT	80227
rs79654663	snp	A/C			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924684	CTGGGGCTGACTGTG[A/C]CCCTGTGTACAAGGT	80227
rs79697609	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73900529	ACAAATAATCCATCC[A/G]GCTGGGCATTTAGAT	80227
rs79797445	snp	A/G	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73913765	AGAAATATTTGGTGA[A/G]TAAATGAATAAATTT	80227
rs79864559	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73915755	TTAGATTTTTAAAAT[C/T]TCCTTCTAGCTCCTG	80227
rs79922652	snp	C/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73914699	TTAAATCCCAGTTCT[C/T]TTTTTTTTTTTTTTT	80227
rs79960388	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876126	CGGGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA	80227
rs80032736	snp	G/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73914716	TTTTTTTTTTTTTTT[G/T]GAGACAGAGTCTCAC	80227
rs80289114	snp	G/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73906297	TCCCTCTGTTACCCA[G/T]GCTGGAGTGTAGTGG	80227
rs80330409	snp	A/C	0.0134861	0.0810011	intron-variant	PAAF1	GRCh38.p7	11:73889887	ATATGCTGGCTAAGA[A/C]AGTGCTGTTTGTGTA	80227
rs80351473	snp	A/C	0	0	intron-variant	PAAF1	GRCh38.p7	11:73893742	AACTCTGTCTCCAAA[A/C]AAAAAAAAAAAAAAA	80227
rs111278886	snp	A/G	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73918762	TTCATGTTTAGAGAC[A/G]TGGATGGTTTTTGAA	80227
rs111278947	snp	C/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73910428	GCATTATAGCTTGGA[C/G]GTGAAACTAAGTGTT	80227
rs111281681	snp	C/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73899361	GGACCACTCTGCATG[C/T]CAGTTGATCTCTTTT	80227
rs111323701	snp	C/G/T	0.00462968	0.0478901	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899205	TTCTAGTACTGACGG[C/G/T]ACCATGAAAATCTGG	80227
rs111360384	snp	C/G/T	0.0267878	0.112589	intron-variant	PAAF1	GRCh38.p7	11:73898661	GTCTCTACCGAAAAA[C/G/T]ACAGAAATAAGGCAC	80227
rs111391827	snp	A/C	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73900244	GGACAAGAGAACTAG[A/C]ATGGAATTTTCTTTT	80227
rs111438930	in-del	-/A	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73894635	AATAATAAAAAAAAA[-/A]TCTACTAAAAAAAAT	80227
rs111523833	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878664	AGGTTGGACTATCTC[A/G]TGTCTAAGTACTATG	80227
rs111538179	snp	A/G	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73924485	CACGTAATAAGATCT[A/G]TTTGCCATTCTGGGT	80227
rs111690592	snp	A/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73893867	AGTTCAAGACCAGCC[A/T]GGACAACATAGTAAG	80227
rs111714301	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73892602	TCTGTCTTTTCCTTA[A/G]ATATTTTACCAAAAT	80227
rs111725624	snp	A/G	0.00835141	0.0640778	intron-variant	PAAF1	GRCh38.p7	11:73917535	AAAATAGCTTCTGTG[A/G]GCATCAGGCTTGGTT	80227
rs111727706	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73913993	GATTCAAGACTGTGG[A/G]GTGCTATGTTTGTGC	80227
rs111853342	snp	A/C	0.0547245	0.156101	intron-variant	PAAF1	GRCh38.p7	11:73882389	TGATGTCAACTCTTA[A/C]GGAGGAGGGTGGTTT	80227
rs111895245	snp	A/G	0.0325976	0.123435	intron-variant	PAAF1	GRCh38.p7	11:73922645	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	80227
rs111936110	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73910649	TCACATTTTAAAAAA[A/T]AGCCCTTATTTTTTA	80227
rs112122721	snp	A/G	0.00795532	0.062565	intron-variant	PAAF1	GRCh38.p7	11:73894462	CTGGCCAACATAATG[A/G]AACCCCATCTCTACT	80227
rs112146109	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876642	CACGAGGCCTGAGGC[G/T]CCTCAGGCGTATCGA	80227
rs112216714	snp	C/T	0.00835141	0.0640778	intron-variant	PAAF1	GRCh38.p7	11:73922053	TTGGCCTTGAACTAA[C/T]AGATGGCTTCATCCA	80227
rs112289987	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73913870	GTGTCTTATCATGGT[A/G]CAAACAACTTAATAT	80227
rs112321955	snp	C/T	0.00795532	0.062565	intron-variant	PAAF1	GRCh38.p7	11:73891056	TTTAAGAGGCTTTAA[C/T]TATAATACATTGGAG	80227
rs112351082	snp	A/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73912946	CAGTGGCACGTTCTC[A/G]GCTCACTGCAACCTC	80227
rs112565977	snp	C/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73883717	AGACGAACGAGGTTT[C/T]GACATGTTGGCCAGG	80227
rs112595258	snp	C/T	0.00318978	0.0398085	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927875	TCCTGTAAGCTGCCA[C/T]CTGGGAGAGATTCTT	80227
rs112617326	snp	G/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73914309	TTTCTTTGTAATAAG[G/T]GAATCGCTAACAAAA	80227
rs112764024	snp	C/G	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73921072	TGGGAGGTCAAGGCG[C/G]GTGGATCAGCTGAGG	80227
rs112768144	in-del	-/TA	0	0	intron-variant	PAAF1	GRCh38.p7	11:73908362	GTGTATATATGTGTG[-/TA]TATATATATGTATAT	80227
rs112863773	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73893766	AAAAAAAAAAAGAAA[A/G]AAAAAACTAAACGTG	80227
rs112906014	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73885952	TACTGAATAATAAAT[G/T]AATGTAGCACCCTGC	80227
rs112915411	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73910338	CCTTTAGAGGATAAG[C/T]TGAAGTTGAACAGAC	80227
rs112988997	snp	C/T	0.031825	0.122064	intron-variant	PAAF1	GRCh38.p7	11:73885679	AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATT	80227
rs113072187	snp	A/G	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73906861	AGTATGCTAAAGACC[A/G]CTAATTAGCTATGTG	80227
rs113093298	snp	C/T	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73899701	ACAGGTGTGAGCCAC[C/T]GCTCCTGGCCTCTCA	80227
rs113108741	snp	C/T	0.5	0	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891183	ATATACTACTTTTTC[C/T]AGAATTCATACAAAG	80227
rs113194077	snp	A/C	0.0267878	0.112589	intron-variant	PAAF1	GRCh38.p7	11:73909072	GATTACAGGTGTGAG[A/C]CACCACGCCCGACCT	80227
rs113202634	snp	C/T	0.5	0	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927517	CTGGCCGTGTGGAAC[C/T]CTCATCCCAAGACCT	80227
rs113283921	snp	A/G	0.0599851	0.162463	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924988	TGAAACCCCGTCTCT[A/G]CTAAAAATACAAAAA	80227
rs113331319	snp	G/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73909235	ATTCATTGGGAAGCT[G/T]GGACTCTATTTCTGT	80227
rs113413367	snp	A/G	0.172997	0.237846	intron-variant	PAAF1	GRCh38.p7	11:73914788	GTTCAGCTCACTGCA[A/G]CCTCCACCTCCTAGG	80227
rs113418808	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73910991	TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA	80227
rs113419662	snp	C/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73902153	AGGTATGAGCCACTG[C/T]GCCTGGCCCAAGTTT	80227
rs113474771	snp	A/G	0.00835141	0.0640778	intron-variant	PAAF1	GRCh38.p7	11:73899812	GTGAAGGTCTAAGTG[A/G]GTGTGCCCTTGTTTT	80227
rs113514363	in-del	-/T	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73921394	GTACTTTTTTTTTTT[-/T]GGAATGTTAGAAATT	80227
rs113555237	snp	C/T	0.00438332	0.0466095	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924935	AGACAGGTGGATCAC[C/T]TGAGGTCAGGAGTTC	80227
rs113606721	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886918	TCTCACTCTGTTCTT[C/T]CCTGAGAAAGCTGAT	80227
rs113738486	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73913441	CTCTATAAAAAATAT[C/T]TTAAAAAATAAATAA	80227
rs113790196	snp	A/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73892891	GGTCTCAATCTCCTG[A/T]CCTTGTGATCCGCCC	80227
rs113973014	in-del	-/AC/ACAC/ACACAC/ACACACAC	0.479119	0.264601	intron-variant	PAAF1	GRCh38.p7	11:73924004	GATAAGTTTATAAAT[-/AC/ACAC/ACACAC/ACACACAC]ACACACACACACACA	80227
rs114085374	snp	A/G	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73906113	AGATGGCAGCAAACC[A/G]TATGGGCTTGATAGA	80227
rs114140150	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73911710	GGCTCACTGCAGCCT[C/T]CACCTCCCAGGTTCA	80227
rs114238167	snp	A/G	0.100231	0.200173	intron-variant	PAAF1	GRCh38.p7	11:73908567	GAGCCACCATACCTA[A/G]ATTAAATTTTTTGTA	80227
rs114314206	snp	A/G	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73925698	TTGACCAGACACTGT[A/G]CTGAACGTTTTATAT	80227
rs114366942	snp	A/T	0.0414363	0.137845	intron-variant	PAAF1	GRCh38.p7	11:73901538	CCCTCTACTTCTGGG[A/T]TTTTTAACTCTGTGT	80227
rs114379925	snp	C/T	0.0322114	0.122752	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887221	ACCTGACTTTTAACA[C/T]AGGCACCTGTTTTTC	80227
rs114467183	snp	C/T	0.0248432	0.108648	intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919321	AGTAAGGCAGACAGA[C/T]GTGTGAACATTTGAT	80227
rs114596612	snp	A/G	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73923097	AAATATATCATGAGC[A/G]TCTTATTTCATCTGT	80227
rs114765540	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875003	AAAACAAACAAACAA[A/T]CAAAGTGAAAGAGTG	80227
rs114969408	snp	C/T	0.0221141	0.102801	intron-variant	PAAF1	GRCh38.p7	11:73905237	GCTGCTTTCTTTTTT[C/T]TTTTGAGACAGAATC	80227
rs115002983	snp	A/G	0.0225045	0.103662	intron-variant	PAAF1	GRCh38.p7	11:73893413	TTAAATCAATAAAAT[A/G]TGAATGTGAAAAGCG	80227
rs115085096	snp	A/C	0.0513262	0.151752	intron-variant	PAAF1	GRCh38.p7	11:73916819	TTTCTGATTTTTCTT[A/C]TTATTCCTGGACTCA	80227
rs115108334	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73906221	ATTTACCTAACAACC[A/G]TTGCCAGCTGTATAA	80227
rs115117795	snp	C/G	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73898617	AGCTCAGGAGTTTGA[C/G]ACTAACTTGGGCAAC	80227
rs115178552	snp	C/G/T	0.0287284	0.116357	intron-variant	PAAF1	GRCh38.p7	11:73925286	ATAAGATGAGACCCC[C/G/T]GTCTCTACAAAAAAT	80227
rs115191766	snp	C/T	0.0123036	0.0774623	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875962	ACATCATTTAATAAC[C/T]TCTCTGGAAGCACAG	80227
rs115195115	snp	A/G	0.031825	0.122064	intron-variant	PAAF1	GRCh38.p7	11:73901073	GGAAATCGTATACTT[A/G]TGTGCTGGGAAATAG	80227
rs115215084	snp	A/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73880225	CCGTGATCATGCTGC[A/G]TGGTCTCCTACCCTG	80227
rs115547074	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73907660	GGTCAACCCCACTGG[A/G]TAGGGGAATGGGAGT	80227
rs115663103	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73911882	CAAGTGATCCACCCT[C/T]CTAAGCCTCCCAAAG	80227
rs115673017	snp	A/C	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73884731	TAGGTCTTCTCTAGG[A/C]CAAACTTCTACCCTA	80227
rs115695777	snp	C/T	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73915653	TGATCAATTAATGAA[C/T]AGACCATTAGTTGAA	80227
rs115695940	snp	A/G	0.00415052	0.0453656	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878857	GCTGTGACTTTAAAG[A/G]AGAAGGATTAATACC	80227
rs115704212	snp	A/G	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73905672	TTTTATTTACTAAAG[A/G]GAGGGTGATAATTTT	80227
rs115730342	snp	C/T	0.0123036	0.0774623	intron-variant	PAAF1	GRCh38.p7	11:73883866	TTTGTGGCCCGGTAA[C/T]ACTCTGTTGTATGGA	80227
rs115766317	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73922952	TGATGCAAATTGCCA[A/G]ACATATCTAAAAGTA	80227
rs115910929	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73906452	AGACGGGTTTCGCTA[C/T]GTTGGCCAGGCTGGT	80227
rs115914792	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73890539	GAGGGAATAGGCACC[A/G]TAAGCCTGACCCAGG	80227
rs115997244	snp	A/G	0.0193772	0.0965046	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876455	TAGGACTCAGTAAAT[A/G]CTGCTGTACTCTCCT	80227
rs116022224	snp	A/C	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73919706	GGGAAATGCCTGGAG[A/C]AAAGTGTACATTAAG	80227
rs116140575	snp	A/G	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73911957	CCTTCTTCTTGCCTA[A/G]TCCACCTTGTTTCTC	80227
rs116313807	snp	A/G	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73911019	AAAAAAAAGTACAGG[A/G]AGTTCTTATATACCT	80227
rs116357699	snp	C/G	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73918342	TTTCTTCCATCATTT[C/G]AGTTACTTAATTTTT	80227
rs116388544	snp	C/T	0.208474	0.246527	intron-variant	PAAF1	GRCh38.p7	11:73882603	AGACATGCGCCACCA[C/T]GCCTGGCTAATTTTT	80227
rs116485660	snp	G/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73915878	TCCATTTTCAAAGTT[G/T]GTTTCAGGAACATTA	80227
rs116486537	snp	A/G	0.0123036	0.0774623	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876244	AACTCTTTAAATAGG[A/G]CCAGGAGCAAATAAT	80227
rs116541145	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902324	TTCAGAGCCTTCCTT[A/T]CATTACTGAAGAACT	80227
rs116558306	snp	A/G	0.0275645	0.114116	intron-variant	PAAF1	GRCh38.p7	11:73894881	CCCAGCTGCTCGAGA[A/G]GCTGGGATGGAAGGA	80227
rs116613500	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73922201	CTGGCATCTTGGTGG[C/T]GCCCGGGTTTCAACC	80227
rs116700386	snp	C/G	0.040671	0.13668	intron-variant	PAAF1	GRCh38.p7	11:73879960	ATCTTAAAAATAAGG[C/G]CAGACGTGGGGGCTC	80227
rs116909381	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886325	CTCTAAAAGCCCTCT[C/T]TACAAATGCTGTATC	80227
rs116922447	snp	C/T	0.0165278	0.0893908	intron-variant	PAAF1	GRCh38.p7	11:73915567	GAGCCAAGATTGCGC[C/T]ACTGTACTCCAGCCT	80227
rs116937815	snp	A/G	0.0267878	0.112589	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888971	AATCCTGTGGGATTG[A/G]CATTTTAAATTTCCA	80227
rs116967011	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73919574	CACTAGCATTTCCAG[A/G]GGGCCTGCTATGTAG	80227
rs117239839	snp	A/C	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73906596	ATTTGAAAAGTTACA[A/C]TATAGTGATTAGGTC	80227
rs117372893	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73919769	CAGGAGGACTGGACT[A/G]TACAGCCTGGAGGGA	80227
rs117503796	snp	C/T	0.00953873	0.0683987	intron-variant	PAAF1	GRCh38.p7	11:73899033	CCTTTTGTTGGGAAA[C/T]ACAGGCTTCAGGAAG	80227
rs117555858	snp	C/T	0.0228947	0.104514	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878327	TCTGTCTTAAATGCA[C/T]AGACCCTTTCCATTA	80227
rs117630947	snp	A/C	0.0119091	0.0762411	intron-variant	PAAF1	GRCh38.p7	11:73923178	GTGATTTTTAATAGT[A/C]ATGCAAAAAAGGGTA	80227
rs117784517	snp	C/T	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73919840	TGTTTTGGGCTGTTA[C/T]TTACAGAACACCCAG	80227
rs117939503	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73895835	AGTGAGGCTGGGCGC[A/G]GTGGCTCACGCCTGT	80227
rs118048881	snp	G/T	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73904669	AGTCATAGCCATTAA[G/T]TTTCCCATATACGCA	80227
rs118117526	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916466	AAAATATAGTGAAAT[G/T]TTTCCTTTTTTGGTG	80227
rs137994746	snp	A/G	0.0360663	0.129354	intron-variant	PAAF1	GRCh38.p7	11:73894781	GTGAGCCGAGGTTGC[A/G]CCACTGCACTCCAGC	80227
rs138053210	snp	G/T	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73915771	TCCTTCTAGCTCCTG[G/T]GATCGTCATCCAGAC	80227
rs138102344	snp	A/C	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73881337	TGTCACCTAGGCTGG[A/C]ATGCAGTGGCATGAT	80227
rs138138027	snp	C/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73883775	ATCCTCCCACCTCGG[C/G]CTCCCAAAGTGCTGG	80227
rs138170812	in-del	-/CT	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73898642	GGCAACATGGTGAAA[-/CT]CTGTCTCTACCGAAA	80227
rs138205134	snp	C/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73915180	GGATTAAATGGTCTA[C/T]TGTTTTGTGATCTTT	80227
rs138396182	snp	G/T	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73905260	ACAGAATCTCACTCT[G/T]TTGCCCAGGCTGGTG	80227
rs138443378	snp	A/G	0.000109041	0.00738301	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891129	AAGCATTCATATTTC[A/G]TGTCCAAAGGAAAAT	80227
rs138468906	snp	C/T	0.00720614	0.0595914	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909508	CTGCTTGGGAGTCCT[C/T]GCAGATTGTGGTTCT	80227
rs138539442	snp	A/T	1.65111e-05	0.0028732	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927314	GAAGCAGATCTACAC[A/T]TGCTGTCGAGACGGT	80227
rs138542789	snp	A/C	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73901830	CCAGCCTCGGCCTCC[A/C]AAAGTGCTGGGATAA	80227
rs138565259	snp	A/T	0.00795532	0.062565	intron-variant	PAAF1	GRCh38.p7	11:73890789	TTGAGAGTATTGGTA[A/T]TAGATTTTCTTCTTA	80227
rs138585730	snp	A/G	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73920305	TTGGGAGGCTGAGGC[A/G]GGAGGATCACTTGAG	80227
rs138610070	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878219	TGCCACTAGCTACCT[A/G]TGAGAAAATACAGCA	80227
rs138738477	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909856	AAAGCAGGGGTGTCC[G/T]ATCTTTTGGCTTCCC	80227
rs138744890	snp	C/G	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73884442	AGAGGCTGCAGTGAA[C/G]CATGATCATACCACT	80227
rs138762502	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910552	AGGTCCTAATAAGGC[A/G]ACTTTCCTTCTTATT	80227
rs138808072	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877684	TGAGGTCAGAAGTTC[C/G]AGACCAGCCTGACCA	80227
rs138861338	snp	C/T	0.0232847	0.105357	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924918	AGTACTTTGGGAGGC[C/T]GAGACAGGTGGATCA	80227
rs139018806	snp	C/T	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73892088	AGCACTTTGAGAGGC[C/T]GAGGTGGGTGGATCA	80227
rs139034390	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73886006	GTTGGGCAAGTCAGA[C/T]ATGTAAACAGTGTGT	80227
rs139234003	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73902280	ATGATGTAAGAAAAC[A/G]GGTACATTGAGAGGG	80227
rs139265499	snp	G/T	0.000363192	0.0134709	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900330	TTCCCATCAGGCCTT[G/T]TGGTCCTGAGTGGGG	80227
rs139272425	snp	C/T	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73904301	TAATTCTAAAATGCA[C/T]TTTAATCAGTTTGAA	80227
rs139355617	snp	C/G	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73892152	ACATGGTGAAACTCT[C/G]TCTCTACAGAAAAAT	80227
rs139429481	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73917277	GCCCGCCTCAGCCTC[C/T]GAAAGTGCTGGGATT	80227
rs139500702	snp	C/G	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73911785	ATTACGGGTGCCCAC[C/G]ACCATGCCTGGCTAA	80227
rs139526210	snp	A/G	0.0364509	0.129988	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874974	CCTGGGTGACAGAGT[A/G]AGACTCCATCTCCAA	80227
rs139565317	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73879108	ACTTCTGCAGCTTCA[A/G]CTGGGACTTTCTTGA	80227
rs139740653	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926752	AGTGTTCCATATTTT[C/G]AATCAACACATTTCC	80227
rs139905714	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903223	CAGGTCACAAAGGCT[C/G]CTTTCCAGTTCGTTG	80227
rs139939688	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73902561	CATCAGTGCACATCC[A/G]GTTTATAAATACCTT	80227
rs139955230	snp	C/T	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73908127	CTACTCTTTCTTGGC[C/T]AAAACCAGAAGTCAT	80227
rs139961047	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73917764	ATAATCCCAGGTACT[C/G]GGGGGCTGAGGCAGG	80227
rs140098568	snp	C/T	1.66813e-05	0.00288797	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927367	CTGACCTCTGACTTC[C/T]TGGAAAGAGCAGTCC	80227
rs140118936	snp	A/G	0.0126979	0.078662	intron-variant	PAAF1	GRCh38.p7	11:73882794	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	80227
rs140228089	snp	C/T	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73902061	GTAGAGATGGGGTTT[C/T]GCTGTGTTGGCTGGG	80227
rs140274405	snp	C/T	0.0528381	0.153711	intron-variant	PAAF1	GRCh38.p7	11:73903487	TTTGGGAGGCCGAGG[C/T]GGGTGGATCATCTGA	80227
rs140276370	snp	C/T	0.00495287	0.0495167	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909590	TCCCCTGAGCAGATG[C/T]CCAGTAAGTTGATAA	80227
rs140291926	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879465	ATTGTAACCGAGGTG[G/T]TACCATTCTAAAACA	80227
rs140330448	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73881778	GTGGTGCAATCTTGG[C/T]TCACTGCAACCTCTG	80227
rs140436852	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927822	CACTCCCTGTTGCCT[A/G]GCCATAGAGAAGGCC	80227
rs140474805	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914763	GATGGAGTGCAGTGG[C/T]GCAATCTCGGTTCAG	80227
rs140484840	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883299	TTATTGAGATAAAAA[G/T]GTGTGCTATCTATGT	80227
rs140585527	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73880009	TCTGGGAGGCCAAGG[C/T]GGAGGATTGCTTGAG	80227
rs140716201	snp	C/T	0.000560483	0.016731	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916568	CTTTATTGGCTCAGA[C/T]GCTTTCAACTGCTGT	80227
rs140858097	snp	C/G	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73895662	GAATTATTGTTGCTG[C/G]GAATGTGTCTGGAAT	80227
rs140949165	snp	C/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73900704	AAGTTGTTTTCTGGC[C/T]GGGCGCGGTGGCTCA	80227
rs141014525	snp	C/T	8.32051e-05	0.00644947	intron-variant	PAAF1	GRCh38.p7	11:73909618	TAATGATATGTAGCA[C/T]TGTTTTATTTTCTTA	80227
rs141120299	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73904091	TCCGTCTCAAAAAAA[A/G]AAAAAGTATATATAT	80227
rs141178319	snp	C/T	0.0325976	0.123435	intron-variant	PAAF1	GRCh38.p7	11:73885303	CACGTGCCACCACAC[C/T]TGGCTAATTTTTGTA	80227
rs141282994	snp	A/G	0.0194964	0.0967888	utr-variant-5-prime, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73876985	ACTCACTTCCGGGAA[A/G]GGGCGGAAGAGGTGG	80227
rs141635536	in-del	-/A	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73907844	CTCAGTCTTTGGGCT[-/A]GGGGCAACAGACTTT	80227
rs141765642	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73919542	AGATGAGGCAAGCGG[A/G]GGCAAAAGAAGAAGA	80227
rs141801030	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73907177	ATAGCAAATATTCAG[A/G]TTATAGATAATAAAG	80227
rs141810612	snp	C/T	0.029116	0.117091	intron-variant	PAAF1	GRCh38.p7	11:73910756	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGATTCA	80227
rs141899558	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73913379	GTGGGCGAATTGCTC[A/G]AGCCCAGGAGTTCAA	80227
rs141902974	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915320	TGAGTAAAGAACTCA[C/G]GCCCACTGGGCATAG	80227
rs141952274	snp	C/G	0.0532157	0.154195	intron-variant	PAAF1	GRCh38.p7	11:73896685	CAAAATGAAAAGTCT[C/G]CCATGTCTACCTCTT	80227
rs142036615	in-del	-/TG	0.0599851	0.162463	intron-variant	PAAF1	GRCh38.p7	11:73920574	TAAAAAGATAGTGAC[-/TG]GGCGTGGTGGCTCAC	80227
rs142243386	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889823	GCTTTATCACACAGT[G/T]AGAAGCAAAAACTCA	80227
rs142283080	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73893820	TCCCAGCACTTAGGG[A/G]GACCCAGAAAGGAGA	80227
rs142297899	snp	A/G	0.0166325	0.0896639	intron-variant	PAAF1	GRCh38.p7	11:73896386	CAATAGTGGAGAGAA[A/G]GTCAGCAGATAAACA	80227
rs142340655	snp	A/G	1.68148e-05	0.0028995	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927375	TGACTTCTTGGAAAG[A/G]GCAGTCCCGGTTAGT	80227
rs142453565	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921671	TCACTGTCCAGGTCT[G/T]GAAAGACTCTAGCAT	80227
rs142573514	snp	A/G	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914432	ACGGGAGGTTGGAAC[A/G]GAGGCCAAAATGCTG	80227
rs142578559	snp	C/T	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73911559	CTCTTCAACCCATTC[C/T]AGGATGGTTTGTGCC	80227
rs142619497	snp	C/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73899865	TTCCAAGACAGAATA[C/G]CTTGGCTGTTAGACT	80227
rs142630038	in-del	-/TTTG	0.0752113	0.178743	intron-variant	PAAF1	GRCh38.p7	11:73906254	TGAATTTCGTTTAGT[-/TTTG]TTTGTTTGTTTGTTT	80227
rs142646200	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875647	AGCAGGTGGTTGAGA[G/T]AGAATCTGACACATG	80227
rs142665451	snp	C/T	9.9108e-05	0.00703876	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927326	CACATGCTGTCGAGA[C/T]GGTCTTGTACGACGC	80227
rs142711222	snp	A/G	0.0236746	0.106192	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877835	AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	80227
rs142754328	in-del	-/AG	0.161596	0.233848	intron-variant	PAAF1	GRCh38.p7	11:73906159	AGACTGAAAAATCTT[-/AG]TTCTCTAGTGGCCTA	80227
rs142765476	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73920923	TGTAATCCCAGCACT[G/T]TGGGAGGCCAAGGCG	80227
rs142867864	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888315	CTCAGTTGCCTGATA[C/T]GGCCATTACCTACTA	80227
rs142970614	snp	C/T	0.0528381	0.153711	intron-variant	PAAF1	GRCh38.p7	11:73882625	CTAATTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	80227
rs143158016	snp	C/T	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73902445	TGCAAGCTTCACCTC[C/T]GATCTGGCCATCCCT	80227
rs143173464	snp	C/T	0.0178098	0.0926698	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924909	TGTAATCCCAGTACT[C/T]TGGGAGGCCGAGACA	80227
rs143228880	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73904602	GAAATTGGCTATGCC[A/G]CCTCCAAGTAATAGG	80227
rs143309456	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903266	CCAGGTTTGGGGTTG[C/T]CCATTCTTCCACAGC	80227
rs143325364	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73913868	TGGTGTCTTATCATG[A/G]TACAAACAACTTAAT	80227
rs143347434	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73902239	AAACACACACATTAA[C/T]CTAAGTACATAAATG	80227
rs143403393	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908194	CAATTATCAGTGAAA[C/G]CAGCAGCAGCATATA	80227
rs143448104	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73903499	AGGCGGGTGGATCAT[C/T]TGAGGTCAGGAGTTC	80227
rs143482857	snp	C/G	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73925275	CAGCCTAGGCAATAA[C/G]ATGAGACCCCCGTCT	80227
rs143544509	in-del	-/AGAGTATATTAT	0.213937	0.247385	intron-variant	PAAF1	GRCh38.p7	11:73916311	GAAAACTGCTACTTC[-/AGAGTATATTAT]AGAGTATATTATATA	80227
rs143571930	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881340	CACCTAGGCTGGAAT[A/G]CAGTGGCATGATCTC	80227
rs143610173	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73883844	TTTTATCAGTACTTC[A/G]TTCCTTTTTGTGGCC	80227
rs143826485	snp	A/C	1.65685e-05	0.00287819	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887438	CTTCAGAAGGATTTA[A/C]TGTGAATGAAATAAA	80227
rs143849479	snp	C/G	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73921505	CCCACTTTCTTTTCT[C/G]CCACCCAAATTCTTG	80227
rs143988079	snp	A/G	0.0178098	0.0926698	intron-variant	PAAF1	GRCh38.p7	11:73916464	TCAAAATATAGTGAA[A/G]TTTTTCCTTTTTTGG	80227
rs143998339	snp	A/G	0.00388617	0.0439088	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891195	TTCCAGAATTCATAC[A/G]AAGAGTGTAAGTATT	80227
rs144025109	in-del	-/GGGGGGGGGG			frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909540	TATCAATGGAGTGGC[-/GGGGGGGGGG]GGTGGGTGCTGCTGA	80227
rs144154138	snp	C/T	1.64743e-05	0.00287	stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909452	GTGGTGTCTGCTTCT[C/T]GAGATGGGACAGCAC	80227
rs144204919	snp	A/C/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73913092	ATGTTGGCCAGGCTG[A/C/G]TCTTAAACTCTTCAC	80227
rs144254333	snp	C/T	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73906510	CCCGCCTCAGACTCC[C/T]AAAGTGCTGGGATTA	80227
rs144295711	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916793	ATTTACAAAGGTTTT[C/G]CAGTCTGAATTTTCT	80227
rs144331277	snp	C/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73922335	TCTGTTTTCAGAGGA[C/T]AAAACTAAGACCAAT	80227
rs144427096	snp	C/T	0.0225045	0.103662	intron-variant	PAAF1	GRCh38.p7	11:73881999	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	80227
rs144506447	snp	G/T	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73894198	TCACCTTTTGAGAAG[G/T]AAGTCATTTTAAAAA	80227
rs144534581	snp	C/G/T	3.29616e-05	0.00405954	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878800	TGAAGGGGAGGCCTG[C/G/T]CTGAGCTGTCATCCC	80227
rs144552449	snp	C/T	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73899514	CCTCCTGGGTTCAAG[C/T]GATTCTTGTGCCTCA	80227
rs144610920	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73896094	AGCCTGAGCAACAGA[A/G]TGAGACCCTGTCTTT	80227
rs144638797	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893311	TTTCCTCTGTAAAAC[A/G]TACCGTTAGGTTGAA	80227
rs144673595	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73901667	GAGTCCAGTGGCATG[A/G]TCTCAGCTCAGTGTA	80227
rs144678394	snp	A/G	0.209693	0.246729	intron-variant	PAAF1	GRCh38.p7	11:73898158	GCTGGGCATCAGAGG[A/G]AGACCGTGGAAAGAG	80227
rs144695799	in-del	-/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877113	AGGCGGGTAGTGGAT[-/G]GTTGCTTTGCGTCAA	80227
rs144997865	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877381	TTAGCAAATATTGAT[C/T]AGTCGTCAGTTACTT	80227
rs145032822	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903186	GAAATGACATGAAGT[C/T]AGATCCAGGCTGGCC	80227
rs145053449	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880392	ATTTTATTGTGCTTA[A/C]TTATGTTCAAAAATC	80227
rs145086702	snp	C/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73879216	TTTCTGCTTAAAGGT[C/G]TCACTGTCACCTTAA	80227
rs145366626	snp	C/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73913672	AATAGTGTGTGATGT[C/G]ATCACATAGAAGATG	80227
rs145438242	in-del	-/G	0.0232847	0.105357	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927681	TTTACAAGGACCTCA[-/G]TACTAAAGCCTGTTC	80227
rs145643997	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914985	ACTGGGAGTACAGAT[A/G]TGAGCCACTGAGCCC	80227
rs145655288	snp	A/G	0.0182019	0.0936463	intron-variant	PAAF1	GRCh38.p7	11:73913661	TTAGCAGTTAGAATA[A/G]TGTGTGATGTCATCA	80227
rs145690792	snp	C/G/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73918511	AGATGGAGTCTTGCT[C/G/T]TGTAGCCCAGGTTGG	80227
rs145695943	snp	C/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73917377	ATGTAGTTTTGATCA[C/T]GACCTTTCTAAACAG	80227
rs145703656	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924405	TTGCTGAGATCATGC[C/G]ATTGTACTCTAGCCT	80227
rs145775059	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73892323	ATGAGACACTGTCTC[A/C]CCAAAAAAAAAAAAA	80227
rs145793470	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918108	GAAGGAGGAAAAGAG[C/T]TGGCCTCGGTAGAAT	80227
rs145837233	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876377	GTTTTCCCATTAATA[A/C]TATTTAATTCGCACA	80227
rs145915332	snp	C/G	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73884307	CAGTTCGAGACCAGT[C/G]TGAGCAACATAGTGA	80227
rs145931872	snp	G/T	0.0283406	0.115616	intron-variant	PAAF1	GRCh38.p7	11:73891689	CTGAGGTGGGAGAAT[G/T]TTTTGAGCCCAGGAG	80227
rs145962598	snp	A/G	0.00597247	0.0543191	intron-variant	PAAF1	GRCh38.p7	11:73890776	GCCCCACTGCTAATT[A/G]AGAGTATTGGTATTA	80227
rs146026715	snp	A/C	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73907534	CCCTGCTGACTGACA[A/C]CTGGGAAGGGGTGGT	80227
rs146109459	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73927197	TTCTCAGACTCCATG[A/G]GACTAGTGTGTGTCA	80227
rs146148572	snp	C/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73886334	CCCTCTCTACAAATG[C/G]TGTATCAAATCTCTA	80227
rs146255488	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73910848	ACAAAAAATTAGTTG[A/G]GTGTGGTAGTGTGTG	80227
rs146294518	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910221	CACCACCATGCCTGG[C/T]AAATTAGCAAGTCCT	80227
rs146377606	snp	A/G	0.00953873	0.0683987	intron-variant	PAAF1	GRCh38.p7	11:73892124	GCTCAGGAGTTCAAG[A/G]CCAGCCTGAGCAACA	80227
rs146429588	in-del	-/TTAA	0.0134861	0.0810011	intron-variant	PAAF1	GRCh38.p7	11:73879055	CATTGTTGATGCATC[-/TTAA]TTAGTCACTTACCCT	80227
rs146495282	in-del	-/TTTAA			intron-variant	PAAF1	GRCh38.p7	11:73904741	TGATAGAGAAACTAA[-/TTTAA]ATAAATACACTTGTT	80227
rs146555845	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918539	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	80227
rs146593067	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880181	AGCTGTGATTATGCT[A/G]CTGGACCTCCTACCC	80227
rs146736332	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909526	AGATTGTGGTTCTTC[C/T]ATCAATGGAGTGGCG	80227
rs146738446	snp	C/T	9.92178e-05	0.00704266	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927339	GACGGTCTTGTACGA[C/T]GCTACCAGCTTTCTG	80227
rs146821622	snp	C/T	0.00557542	0.0525036	intron-variant	PAAF1	GRCh38.p7	11:73883146	GTTTATTTTTTAATA[C/T]ATGGGGTCTCGCTGT	80227
rs146833784	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887612	TCATTGGTATTTTCT[A/G]TTGTAGTTACATATA	80227
rs146975513	snp	A/G	0.00914312	0.0669923	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924991	AACCCCGTCTCTACT[A/G]AAAATACAAAAAAAT	80227
rs146986148	in-del	-/GTT	0.0126979	0.078662	intron-variant	PAAF1	GRCh38.p7	11:73895718	GAGCATTTGCAGCTG[-/GTT]GTTTTTTAATAAAAG	80227
rs147008634	snp	C/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73883709	TTCAGTAGAGACGAA[C/T]GAGGTTTCGACATGT	80227
rs147018562	snp	A/G	0.00398564	0.0444627	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888654	ATAAGATTTTTAGCA[A/G]ATGTTCATTCATTAC	80227
rs147080781	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73904760	AATACACTTGTTAAG[A/G]ATATACACCTGGGAA	80227
rs147090224	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73909197	CTTGTTTTTCCATGC[C/T]TGTCTTTCACAGCTA	80227
rs147150069	snp	A/G	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73879430	CAACAGTCTTATATC[A/G]TTCACAGGATTCTTT	80227
rs147160088	snp	C/T	0.0158469	0.0875917	intron-variant	PAAF1	GRCh38.p7	11:73881414	CCTCAGCCTCCTGAA[C/T]AGCTGGGACTACAGC	80227
rs147312150	snp	A/G	1.67094e-05	0.0028904	splice-acceptor-variant	PAAF1	GRCh38.p7	11:73899145	TTTTCTCTTTGAACA[A/G]ATAACATGCCTGGAC	80227
rs147364177	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916796	TACAAAGGTTTTCCA[A/G]TCTGAATTTTCTGAT	80227
rs147373771	snp	A/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73920944	GGCCAAGGCGGATAG[A/T]TCACCTGAGGCCTTG	80227
rs147467793	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73898250	AGAGGGAGAGGGAGA[A/G]GGAGAGGGAGAGGGA	80227
rs147479329	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902514	AGTCATGACTCAGCA[C/T]GTTGAACTTAATTAA	80227
rs147550776	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875210	CACTCAGCAGAAAGC[A/G]GCATACAGAAGGAAC	80227
rs147645028	snp	A/G	0.000193817	0.00984231	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889164	TTCTTTCTTCCCTTC[A/G]TACTCAGACCTGGAT	80227
rs147760602	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73913369	GGAGGCTGAGGTGGG[C/T]GAATTGCTCGAGCCC	80227
rs147863969	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893661	AGAATCGCTTGAACG[C/T]GGGAGGCAGAGGTTG	80227
rs147962648	snp	A/G	0.0520825	0.152737	intron-variant	PAAF1	GRCh38.p7	11:73908888	ACGCCTCCCAGGTTC[A/G]AGCGATTCTCCTGCC	80227
rs147990569	snp	A/G	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73891521	TGGCTCACACCTGCA[A/G]TCCTAGCACTTTGGG	80227
rs148061252	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919322	GTAAGGCAGACAGAC[A/G]TGTGAACATTTGATT	80227
rs148117364	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876846	CTCTGTACATCCTTT[C/T]AGGAACCAGCCCCTC	80227
rs148279230	snp	C/T	0.0260105	0.111035	intron-variant	PAAF1	GRCh38.p7	11:73880611	AGAATGGAGTGAACC[C/T]GGGAGGCGGGGCTTG	80227
rs148331294	snp	A/C	0.0115144	0.0749975	intron-variant	PAAF1	GRCh38.p7	11:73914737	AGAGTCTCACTCTGT[A/C]GCCCAGGTTGGATGG	80227
rs148347769	in-del	-/AAAT	0.0456336	0.143994	intron-variant	PAAF1	GRCh38.p7	11:73898833	AACAAACAAACAAAC[-/AAAT]AAATAAATGCAACAC	80227
rs148454913	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73910882	GTAATCCCAGCTACT[C/T]GGGAGGCTAAGGCAG	80227
rs148478675	snp	C/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900318	TGTTGCAGGTTTTTC[C/T]CATCAGGCCTTGTGG	80227
rs148537189	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887983	TCGAACTCCTGACCT[C/T]GTGATCCACCTGTCT	80227
rs148586455	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73882358	AGATTCAGTTTTCTT[C/T]ATGAATTGGAGTTAA	80227
rs148640249	snp	A/G	0.000216322	0.0103978	intron-variant	PAAF1	GRCh38.p7	11:73916533	GCATTTTTGCCTCCT[A/G]CTTGTTCCCAGGTGT	80227
rs148715773	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73906772	GGATTGGCACTTGTA[C/T]GTTACGCTGAGTTGC	80227
rs148734141	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73893090	CAGTTTTATATTACT[A/G]GACATTCAGGTGTTT	80227
rs148800310	snp	C/T	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73921546	TTTCAAGTAAAGACA[C/T]GGTCTTCTCTCTTCT	80227
rs148912854	snp	A/G	0.0166325	0.0896639	intron-variant	PAAF1	GRCh38.p7	11:73883678	CCTGCCACCACACCC[A/G]GGTAATTTTTGTATT	80227
rs148974912	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876492	ACCTTTTGGCTTCAG[A/T]CTCCTCTGGAGTAAA	80227
rs148999050	snp	C/G	8.24763e-05	0.00642116	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887372	AACCATCTTTGTATG[C/G]CAGCCTGACTTGTCA	80227
rs149124136	snp	A/C	0.00318978	0.0398085	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924837	TGTGGTAGGATGGCA[A/C]GAAATCAAGAGCTTA	80227
rs149131885	in-del	-/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876819	TTGGGTTTCGCAGGC[-/G]GGTTGGGGATCCTCT	80227
rs149186632	snp	G/T	0.0107246	0.0724382	intron-variant	PAAF1	GRCh38.p7	11:73913810	TGTAAGATCTTTGAG[G/T]TCAGAGACTGTTTTT	80227
rs149248741	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73881851	AGCTAGGACTACAGG[C/T]GCGTGCTACCATGCA	80227
rs149282047	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890989	GGTGGGAAAGGAGAA[C/T]GAGAGAGGGTACACT	80227
rs149302262	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878741	GGATCCTATTCAACT[C/T]TGGGTAAGCCTAATT	80227
rs149355526	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73909921	ATAAAATACACAACA[C/T]TGATGATAGCTGAGC	80227
rs149515881	snp	A/G	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73915776	CTAGCTCCTGTGATC[A/G]TCATCCAGACAACTT	80227
rs149577547	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73905350	TGCCTCAGCTTCCCA[A/G]GTAGCTGGGACTACA	80227
rs149647921	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73886218	ATGTATTATGTGTAT[A/G]TACTGTAGATAAATA	80227
rs149848516	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875826	AATCACAAGAGGGAG[A/T]TAGGCACTTTACACA	80227
rs149948901	snp	A/G	0.000116892	0.00764409	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900409	TGGTGACCTTCAAAG[A/G]TCACAAAGGAGGTAT	80227
rs149954457	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902894	TTAGTAGAGACTGGG[A/T]TTCACCATATTGGCC	80227
rs149973774	snp	C/G	0.00358779	0.0422022	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927839	CCATAGAGAAGGCCT[C/G]CTTGGCAGTAGCAAT	80227
rs150041384	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73880177	AGTGAGCTGTGATTA[C/T]GCTACTGGACCTCCT	80227
rs150151107	snp	C/T	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73920282	CTCATGCCTATAATC[C/T]CAGCATTTTGGGAGG	80227
rs150194850	in-del	-/ACTGCA	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73914782	ATCTCGGTTCAGCTC[-/ACTGCA]ACCTCCACCTCCTAG	80227
rs150195524	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73923432	GATCAAAATGTTAAC[A/G]GTAATTGCCTTTGAA	80227
rs150212844	snp	C/T	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73909756	ACTATGTTTCTATTA[C/T]TTTGGAATCTACAAA	80227
rs150270418	snp	A/G	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73904248	TGGAAAGGTAGACTA[A/G]AAGTAGTTTTGTGAT	80227
rs150288675	snp	C/T	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73902093	TGGTCTTAAACTGGC[C/T]TCAAGTGATCTGCCT	80227
rs150332375	in-del	-/AAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73892326	AGACACTGTCTCACC[-/AAAAAAA]AAAAAAAAAAGAAAG	80227
rs150404250	snp	C/G	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73883379	ATACCCATTAACAGT[C/G]ACTTTCCACCCCCCA	80227
rs150469758	snp	A/G	6.59457e-05	0.00574182	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916607	CTCTGGCTTCTTGCT[A/G]TTGGCTGGGACTCAA	80227
rs150532100	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73911566	ACCCATTCTAGGATG[A/G]TTTGTGCCCAAGTAC	80227
rs150583440	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878094	GCCTTCTGCATTTAA[A/G]AAATTTACACCTTAC	80227
rs150602517	snp	C/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73902729	TGAGATGGAGTCTCA[C/G]TCTGTCTCCTAGGCT	80227
rs150721320	snp	C/T	0.0225045	0.103662	intron-variant	PAAF1	GRCh38.p7	11:73885810	TCACGCCATTGTACT[C/T]CAGCCTGGGCGACAA	80227
rs150724739	in-del	-/CA/CACACC/CACC			intron-variant	PAAF1	GRCh38.p7	11:73924027	ACACACACACACACA[-/CA/CACACC/CACC]CCTGTGGTTGCTTGC	80227
rs150741541	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874767	CCGAGGCAGATGGAT[C/T]ATAAGGTCAGAAGTT	80227
rs150774895	snp	A/G	0.0275645	0.114116	intron-variant	PAAF1	GRCh38.p7	11:73880859	CAAAAAATTACCTGG[A/G]CGTGGTGGTGCATGC	80227
rs150819008	snp	C/T	0.000153988	0.00877327	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900329	TTTCCCATCAGGCCT[C/T]GTGGTCCTGAGTGGG	80227
rs150921020	snp	A/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73903815	TTGGCCGGGCGCAGC[A/G]TCTCACCCCTGTAAT	80227
rs150921516	snp	C/G/T	0.000280123	0.0118317	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914450	GGCCAAAATGCTGCT[C/G/T]TTGGCCCGGGAAGAT	80227
rs151048167	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888351	AACAATGTAGCCTTA[C/T]AATCCATATCTGGTG	80227
rs151255226	snp	C/T	0.00478085	0.0486577	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927790	AGTTGGTCAGGACGA[C/T]GGAATTCCTTCCTCA	80227
rs151321723	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73879777	ACTTGGGAGGCTGCA[A/G]TAGGAGGATCTCTTG	80227
rs180784687	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73890720	TGTTGAAGAGTTTCC[G/T]TATATCTCTTTATGT	80227
rs180793731	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923967	AGACATTTTTTAGAC[A/G]TTCCCTATTAAATAT	80227
rs180795437	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906416	TGCCACCACACCTGG[C/T]TAATTTTTGTATTTT	80227
rs181039716	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908731	ACTGAATTAGCTTAG[C/G]TGTCAACTTTTTTTT	80227
rs181053511	snp	C/G/T	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73894876	GTAGTCCCAGCTGCT[C/G/T]GAGAGGCTGGGATGG	80227
rs181064496	snp	A/C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903280	GCCCATTCTTCCACA[A/C/G]CGTGGCAAAAATCAG	80227
rs181073959	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73920678	GCCAACATGGTGAAA[C/T]GCTGTCTCTACTAAA	80227
rs181093207	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924433	CCTGGGCAAAAAGAA[C/T]GAAACTCTGTCTCAA	80227
rs181301152	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73895702	TGGTCCATCATTTCT[A/G]GAGCATTTGCAGCTG	80227
rs181323442	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73926664	CAGTGAGCCAAGATG[A/G]CGTCACTGCACTCCA	80227
rs181325929	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904035	GTTGCATTGAGCCAA[C/G]ATTGCACTACTTCAC	80227
rs181329118	snp	C/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73920808	AGTAAGCTGAGAGCA[C/T]GCCACTGCACTCCAG	80227
rs181414634	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73908961	GCCTGGCTATTTTGT[A/G]TTTTTAGTAAAGACA	80227
rs181471448	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73895969	TAAAAAATTAGCTGG[A/G]CATGCCAGCCCATGT	80227
rs181621398	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885306	GTGCCACCACACCTG[C/G]CTAATTTTTGTATTT	80227
rs181644457	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73920145	CTGAAACTGATTAAG[A/G]GCATATGGGAACCTT	80227
rs181661975	snp	C/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73880579	GTAGTCCCAGCTACT[C/T]GGGAGCCTGAGGCAG	80227
rs181684818	snp	A/C	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73899317	TGGACTGGGACATGG[A/C]AGGAAGAATGGCCCA	80227
rs181720139	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902758	CTGGGGTGCAGTGGC[A/G]CGATCTTGGCTCACT	80227
rs181902797	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73907213	CAAAAACTATAAAAT[C/T]GATAGGCATTTTGGA	80227
rs181936489	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73890275	CTTTTTCTTTTTTTT[A/G]CCTCTACACGTGCTA	80227
rs181950187	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906404	ATTACAGGCACCTGC[C/T]ACCACACCTGGCTAA	80227
rs182164449	snp	C/G	4.95242e-05	0.0049759	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900359	GGGAATGGATGCCCA[C/G]CTGAAGATATGGTCA	80227
rs182168407	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891619	TGTCTCCACAAAAAA[A/T]CAAAAATTAGCTGAG	80227
rs182192460	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882703	CGCCTTCCAGGTTCA[C/T]GCCATTCTTCTGCCT	80227
rs182233181	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914587	TTTTGGAAACATTTC[C/T]ACTTGCTCCCTGTGT	80227
rs182436007	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73881867	GCGTGCTACCATGCA[C/T]GGCTAATTTTTTGTA	80227
rs182448925	snp	A/G	0.00716266	0.059414	intron-variant	PAAF1	GRCh38.p7	11:73913449	AAAATATTTTAAAAA[A/G]TAAATAAAGTTGAAG	80227
rs182495382	snp	A/C	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73901292	TCAGATTATAGATAT[A/C]CAGTGGGAACATCTT	80227
rs182507482	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73914948	TGACTCAAGTGATCC[A/G]CCTGCCTCAATCTCC	80227
rs182532951	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924924	TTGGGAGGCCGAGAC[A/G]GGTGGATCACTTGAG	80227
rs182742331	snp	A/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875752	AAGTAAGTGATCATC[A/T]CAAGGCTTTGTAGGA	80227
rs182747217	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897667	CTTTCCAGACTGGGC[A/G]GCCGGGCAGAGAGGC	80227
rs182787431	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908287	TATGTGTATATATGT[A/G]TATATATGTGTGTAT	80227
rs183013557	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911505	AATTTAAATGAGAAT[A/T]TTTTTTCTTGTTTTC	80227
rs183037052	snp	C/G	0.496681	0.0405994	intron-variant	PAAF1	GRCh38.p7	11:73896951	ccagacctccctccc[C/G]gacggggcggctggc	80227
rs183064695	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888361	CCTTATAATCCATAT[C/G]TGGTGAGGCCTTGAT	80227
rs183084287	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905440	TATTGGCAAGGCTGG[C/T]CTCAAACTCCTGACC	80227
rs183086437	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921473	TGCTGCAGAAAATTT[A/C]AAATCACTGTTGATA	80227
rs183320564	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886916	GTTCTCACTCTGTTC[C/T]TTCCTGAGAAAGCTG	80227
rs183340461	snp	A/C	0.0232847	0.105357	intron-variant	PAAF1	GRCh38.p7	11:73892288	TGATCATGCCACTGC[A/C]CTCCAGCCTGGGCAA	80227
rs183341517	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73907859	AGGGGCAACAGACTT[C/T]ACTGGGAGTTTTGTT	80227
rs183349843	snp	A/C			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924770	TATGAGACTGAATCC[A/C]GATACCTTGTGGTCA	80227
rs183353725	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911104	GTGGTACATTTATTA[C/T]AGCTGATGAACCTAC	80227
rs183362420	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888045	GAGCTACCATGCCCA[A/G]GCGAAATTGATTTTA	80227
rs183373688	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73920969	GCCTTGATATTTCTC[A/G]CCTCCTCTGTCCTAT	80227
rs183584905	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73883989	AGATGGCATGAGAAC[C/T]AGCTGCTGTGGGGAA	80227
rs183601291	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73902008	AGCTGGGATCACAGG[C/T]GTGCACCACCACATC	80227
rs183604350	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73905076	TGTGATATAATTGTG[C/T]CTGTGAATAGCAATG	80227
rs183606722	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73918398	TGCCTCCACAGAGAT[A/G]GGGAATCTCTGATCA	80227
rs183630096	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73883101	AGACAAGGTCTCACT[A/G]TGTTGCCCAGGCTGG	80227
rs183640990	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73910156	TTGAACTCCTGGGCT[C/T]AAGTGATGCTCCCAC	80227
rs183847696	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73919540	ATAGATGAGGCAAGC[A/G]GGGGCAAAAGAAGAA	80227
rs183962927	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73901724	TACGGGTACACGCCC[C/T]ACACCTGGCTAATTT	80227
rs183986287	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893629	ATAATCCCAGCTACT[C/T]GGGAGGTTGAGGCAG	80227
rs184092736	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880345	ATACTTAACATAAAA[A/G]TTCAAGGAAAATACT	80227
rs184094126	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73921767	TCTCACAAAGTCTCA[A/G]CCCAGTCTCTTGCCT	80227
rs184101289	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73898686	AGGCACAGTGGTGTG[C/T]GCCTGTAGTCCCAGC	80227
rs184102472	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912901	TTTTTTAAATTGAGA[C/T]GGAGTTTCCCTCTTT	80227
rs184129195	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883411	TCCTAGCAACCACTA[G/T]TTTACTTTCTAGCTC	80227
rs184151882	snp	A/C	0.0123036	0.0774623	intron-variant	PAAF1	GRCh38.p7	11:73916340	TAACCTGCTCAAGTC[A/C]TTAGTCAACCCCAGG	80227
rs184323191	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73895235	TCAAAAAATTTTGGC[C/T]TGAGAAGTAGGTGAA	80227
rs184345047	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73926473	CAGCACTTTGGGAGG[C/T]GGAGGGGGTGCGAAT	80227
rs184464246	snp	C/T	0.00557542	0.0525036	intron-variant	PAAF1	GRCh38.p7	11:73908849	GCTGGAGTGCAGTGG[C/T]GTGATCTCGGGTCAC	80227
rs184474149	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877606	AAGCTGACATCCAGG[A/C]CAGGCGCAGTGGCTC	80227
rs184585489	snp	A/G	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73908375	TGTATATATATATGT[A/G]TATATATGTGTGTAT	80227
rs184593092	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884502	CCTGTCTCAAATATT[A/T]AAAAAATACATATAT	80227
rs184721329	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902279	CATGATGTAAGAAAA[C/T]GGGTACATTGAGAGG	80227
rs184721702	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73925946	GACTATTTTCAGAGA[A/G]TTTGCACACTTACAT	80227
rs184769384	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890580	TTATGGGTGTACCAT[A/T]ATTTACTTTACCAAT	80227
rs184771062	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906408	CAGGCACCTGCCACC[A/T]CACCTGGCTAATTTT	80227
rs184774370	snp	G/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73922695	CATGGCGGGCGCCTG[G/T]AGTCCCAGCTACTTG	80227
rs184870247	snp	C/T	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73906246	GTATAAATTGAATTT[C/T]GTTTAGTTTTGTTTG	80227
rs184980023	snp	C/T	0.00119737	0.0244387	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889179	ATACTCAGACCTGGA[C/T]ACAGTCTTTATCACT	80227
rs185018164	snp	A/C	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73908584	TTAAATTTTTTGTAC[A/C]GACAGAGTCATGCTG	80227
rs185019783	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894606	CTGCACATTGTGCAC[A/G]TGTACCCTAAAACTT	80227
rs185033583	snp	C/T	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73926119	TTTCTTTCTTTCTTT[C/T]TTTTGAGATGGAGTT	80227
rs185134310	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889703	TTTGAAGCTCCTTGC[A/T]TCCTTGCTAATATGA	80227
rs185162880	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73922632	ACCATCCTGGCTAAC[A/G]TGGTGAAACCCCGTC	80227
rs185262005	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906348	ACCTCTGCCTCTCGG[A/G]TTCAAGTGATTCTTG	80227
rs185313176	snp	A/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73903792	ATAAAAAGAAACATT[A/T]AAAAAAATTGGCCGG	80227
rs185325049	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895845	GGCGCGGTGGCTCAC[A/G]CCTGTGATCCTAGCA	80227
rs185329069	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920686	GGTGAAACGCTGTCT[C/G]TACTAAAAATACAGA	80227
rs185342726	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909200	GTTTTTCCATGCCTG[A/T]CTTTCACAGCTAGAC	80227
rs185398788	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73879398	AGCTCCCAAGTCTTA[C/T]CAATTTTTCTTTTGA	80227
rs185403992	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912184	TCTGGGCCCTCAGCT[A/G]TAACTACAGTTTCTT	80227
rs185517599	snp	C/T	0.107341	0.205301	intron-variant	PAAF1	GRCh38.p7	11:73898048	ACCAGTCAGGCGTGG[C/T]GGCGCGCGCCTGCAA	80227
rs185819755	snp	C/T	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73920454	GAGGATCACTTGAAT[C/T]TAGGAGGTGAGGCTG	80227
rs185834581	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73882752	GGATTACAGGTGTCC[A/G]CCACCACGCCCAGCT	80227
rs185855522	snp	A/C	0.02016	0.0983543	intron-variant	PAAF1	GRCh38.p7	11:73899666	ATCTGCCCACCTTGG[A/C]CTCCCAAAGTGCTGG	80227
rs185868695	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913224	TATACTCCTGCAGGT[A/C]TTCACATGACTGGTT	80227
rs185870871	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891884	ATTTCAAATATACCA[C/T]ATTGAGGAATAATTT	80227
rs186109865	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910572	TCCTTCTTATTTTCC[C/T]ATAATAATAGTTGCA	80227
rs186235366	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887792	TCTTGCTCTGTCGCC[C/T]AGGCTGGAGTGCAAT	80227
rs186251722	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920875	AAAAAAATTAAAAAT[G/T]AAAAAATAAGGTTGG	80227
rs186390267	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926844	TAGTTGGTAGTAAAG[C/T]TGAGACTAACTCCAG	80227
rs186394962	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73904818	TATTTATTTCAGGAA[C/T]AGTTTCATCTAATGT	80227
rs186414695	snp	G/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73896136	AAAAACTATAAAAGT[G/T]AGTTTGGAAAACAAA	80227
rs186420411	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909808	GCGTTTCAGTAAGTA[C/T]AATCTAATGTAGAAG	80227
rs186421983	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927507	GTCAGCTGTACTGGC[C/T]GTGTGGAACTCTCAT	80227
rs186499049	snp	A/C	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73906633	GAGTTGCTTTTAATG[A/C]TATTTTCTCACACAG	80227
rs186681909	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888776	CTAAGTCTTAGTTAA[C/T]TCTGACACTTATTAG	80227
rs186695964	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905606	TTTCTTTATTCTTGT[C/T]GTGTAAGTGTTAAGA	80227
rs186697069	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921526	CAAATTCTTGATCAA[C/G]AGTTTTTCAAGTAAA	80227
rs186706660	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73890900	ATAATGGCATCTTAG[C/T]AATACCAAATTACAC	80227
rs186711100	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924127	AAATCCAGCCCAGCT[C/T]AGCATTCTAGGCAGC	80227
rs186787776	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924456	TGTCTCAAAAAACAA[A/C]AAAAAAGTTGGCCCA	80227
rs186950270	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73880826	TAACATGGTGAAGCC[C/G]TGTTTCTACTAAAAA	80227
rs186982227	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907477	TTGCACCACCTGACT[G/T]GCATCACCTCATTGC	80227
rs187057482	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73881943	GCAATGGTGCCATCT[C/T]GGCTCACTGCAACCT	80227
rs187070433	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913865	GTGTGGTGTCTTATC[A/G]TGGTACAAACAACTT	80227
rs187071361	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876719	CAGCCCCGTTGTGCC[A/C]GCAACGCCTCCTGAA	80227
rs187082202	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73911119	CAGCTGATGAACCTA[C/T]GTGACACATTATTGT	80227
rs187247600	snp	A/T	4.95446e-05	0.00497693	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900372	CAGCTGAAGATATGG[A/T]CAGCTGAAGATGCTA	80227
rs187351868	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73902760	GGGGTGCAGTGGCGC[C/G]ATCTTGGCTCACTGC	80227
rs187543740	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915126	CTCTCTGAGCCTGCT[G/T]CCTCATCACTAAACT	80227
rs187546908	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73893630	TAATCCCAGCTACTC[A/G]GGAGGTTGAGGCAGG	80227
rs187560573	snp	A/G	0.046775	0.145601	intron-variant	PAAF1	GRCh38.p7	11:73908409	TATATGTGTATATAT[A/G]TGTGTGTATATATAT	80227
rs187572857	snp	A/G	0.00953873	0.0683987	intron-variant	PAAF1	GRCh38.p7	11:73926058	TTTTTTTTAATTACC[A/G]TCTTAGAGCTGTTTC	80227
rs187596574	snp	A/G	0.0984431	0.198823	intron-variant	PAAF1	GRCh38.p7	11:73885627	TGGGTGGATCACCTG[A/G]GGGGAGGAGCTCAAG	80227
rs187607223	snp	C/T	0.0539704	0.155153	intron-variant	PAAF1	GRCh38.p7	11:73896954	GACCTCCCTCCCCGA[C/T]GGGGCGGCTGGCCGG	80227
rs187644157	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908175	GGAGGCTAACCCTTT[G/T]AATCAATTATCAGTG	80227
rs187645575	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892377	CTTTTTCACCCTTAT[G/T]ACAAAACAGATATAT	80227
rs187679541	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924885	GGGCCAGGCATGGTG[C/G]CTCACGCCTGTAATC	80227
rs187821251	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73905326	CCTCCTGGGTTCAAG[A/T]GATTCTTCTGCCTCA	80227
rs187885337	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874901	TCAGGCAGGAGAATC[A/G]CTTTAACCCAAGGGG	80227
rs187903420	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889336	TGTTCTCTTAAACAG[C/T]AGATCTGTCATTATG	80227
rs187904946	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888178	TCTTCAAAACTCCAT[A/G]TATATTTTACTTTTA	80227
rs187913162	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73922437	CTGCCCTTAAGGTAG[G/T]GGGCACCCCTAACTC	80227
rs187957699	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918518	GTCTTGCTCTGTAGC[C/T]CAGGTTGGAGTGCAG	80227
rs188080933	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911789	CGGGTGCCCACCACC[A/T]TGCCTGGCTAATTTT	80227
rs188152562	snp	A/G	0.0107246	0.0724382	intron-variant	PAAF1	GRCh38.p7	11:73908301	TATATATATGTGTGT[A/G]TATATGTATATATAT	80227
rs188194337	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73906322	TAGTGGTGCAATCTC[C/T]GCTCACTTCAACCTC	80227
rs188367416	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73906409	AGGCACCTGCCACCA[C/T]ACCTGGCTAATTTTT	80227
rs188367598	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890711	GGGGGATGGTGTTGA[A/G]GAGTTTCCTTATATC	80227
rs188380802	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73923575	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	80227
rs188404345	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901430	GAATATTTTAAAAAT[A/G]TGTGATAATATCCCC	80227
rs188426914	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73893005	GTCCATTATTCTATG[C/G]TGTCTTTCAATGTAT	80227
rs188474063	snp	G/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73880557	CCGGATGTGGTGGTG[G/T]GCCCCTGTAGTCCCA	80227
rs188494158	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73898757	AGGCAGAGGTTGCAG[C/T]GAGCTGAGATGGGGA	80227
rs188502281	snp	C/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73913001	CCCGCCTCAGCCTCC[C/T]GAGTAACTGGGATTA	80227
rs188685455	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883529	TTTCTTTCTTTCTTT[G/T]TTTTTTGAGAGTCTC	80227
rs188692490	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73883156	TAATACATGGGGTCT[C/T]GCTGTGTTTCCCAGG	80227
rs188722777	snp	A/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73884112	TACTCAGCAGCCTGC[A/T]TGTAGGAATGTAGAA	80227
rs188742931	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902036	ATCCAACTAATTTTT[C/G]TATTTTTTAGTAGAG	80227
rs188873604	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906388	CTCCCAAGTAGCTGG[A/G]ATTACAGGCACCTGC	80227
rs188939561	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73905079	GATATAATTGTGCCT[C/G]TGAATAGCAATGGCA	80227
rs188943496	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878137	TTACTTAATTTAGGT[A/G]GGCTAAAATACAGAC	80227
rs188975891	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901772	ATGGGGTTTCACCAT[A/G]TTGGTCAGGCTGGTC	80227
rs188987576	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908873	GGGTCACTGCAACCT[A/G]CGCCTCCCAGGTTCG	80227
rs189031874	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909278	TGAACATGGCCAGCA[C/T]GTGGTACCTGTTCAG	80227
rs189045996	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73927165	TATGGATGTAATTCT[G/T]TTGCCTTCATAAAGC	80227
rs189225733	snp	A/G	0.0107246	0.0724382	intron-variant	PAAF1	GRCh38.p7	11:73898164	CATCAGAGGGAGACC[A/G]TGGAAAGAGAGGGAG	80227
rs189227240	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73921190	CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAGGC	80227
rs189233664	snp	A/G	0.0532157	0.154195	intron-variant	PAAF1	GRCh38.p7	11:73897973	ATCACTCATGGTTAG[A/G]AGCTGCAGACCAGCC	80227
rs189260670	snp	C/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73895245	TTGGCCTGAGAAGTA[C/G]GTGAATTGTGTTCCA	80227
rs189287658	snp	A/G	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73926634	GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC	80227
rs189402247	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73894738	CTAAGGCACAAGAAT[C/T]GCTTGAACCCAGGAG	80227
rs189406150	snp	G/T	0.0966517	0.197444	intron-variant	PAAF1	GRCh38.p7	11:73885628	GGGTGGATCACCTGA[G/T]GGGAGGAGCTCAAGA	80227
rs189410588	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908628	GGTCTTAAACTCCTG[C/T]GCTCAAGAGATTCTC	80227
rs189417000	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73926183	GCGATCTCAGCCCAC[A/T]GCAACCTCCGCCTCC	80227
rs189426713	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902993	GTGAGCCACTGCGCC[C/T]GGCCTAGAATGTTAA	80227
rs189513543	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73879664	TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA	80227
rs189530578	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912267	ATAGACCTTTCACCT[C/G]AGTTTCAGACTCTAT	80227
rs189642902	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890274	CCTTTTTCTTTTTTT[G/T]ACCTCTACACGTGCT	80227
rs189668232	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886531	ATACAAAAAATTAGC[C/T]GACATGGTGGCGGGT	80227
rs189678148	snp	A/T	0.00716266	0.059414	intron-variant	PAAF1	GRCh38.p7	11:73903830	GTCTCACCCCTGTAA[A/T]CCCAGTACTTTGGGA	80227
rs189690610	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73920705	TAAAAATACAGAAAT[C/T]AGCTGGCATGGTGGC	80227
rs189796364	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881534	CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	80227
rs189816782	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73913320	AAAGTTTAGGCTGGA[C/T]GTGGTAGCTCACGCC	80227
rs189842885	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908265	TATATATGTATATAT[A/G]TGTATATATGTGTAT	80227
rs189848907	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924907	CCTGTAATCCCAGTA[C/T]TTTGGGAGGCCGAGA	80227
rs189945151	snp	A/C	0.00755907	0.0610114	intron-variant	PAAF1	GRCh38.p7	11:73882040	CCACCATGCCTGGCT[A/C]ATTTTGTATTTTTTT	80227
rs190055371	snp	A/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73902706	TATTTATTTATTATT[A/T]TTTTTTTTGAGATGG	80227
rs190059306	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73900134	CTAAGAGATCCTTTG[A/G]ATATCCTTAGTTTTA	80227
rs190213266	snp	A/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73882760	GGTGTCCGCCACCAC[A/G]CCCAGCTAATTTTTT	80227
rs190231819	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73901065	CCTCTCCAGGAAATC[A/G]TATACTTGTGTGCTG	80227
rs190235351	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914930	AGACTAGTCTCAAAC[C/T]CCTGACTCAAGTGAT	80227
rs190308909	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73885284	TCATAGCTGGGACTA[C/T]AGGCACGTGCCACCA	80227
rs190324995	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920050	GTGAAAAAAAAAAAG[C/T]ATGCTGTTTAGGTGG	80227
rs190333802	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892035	TTTTTTAAAAGAGCA[A/G]TTTTTGGCCAGGCAC	80227
rs190343556	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920502	GCCACTGCATTTCAC[C/G]CTGGGTGACAAAGCG	80227
rs190350408	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907499	CCTCATTGCCTTCTA[A/G]TGGCGTTATAAGCTT	80227
rs190351873	snp	A/T	0.000164739	0.00907428	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924645	TTATTGTCCAGCAAG[A/T]CTTAGACTATGTCAC	80227
rs190592980	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73895932	GGCAACATAGGGGGA[C/G]CCCATCTCTCCAAAA	80227
rs190627422	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875016	AAACAAAGTGAAAGA[G/T]TGCCCAAATATGGGT	80227
rs190645436	snp	C/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73910772	GAGGCGGGCGATTCA[C/T]AAGGTCAGGAGCTCG	80227
rs190878774	snp	A/G	0.0663309	0.169604	intron-variant	PAAF1	GRCh38.p7	11:73897434	CTTCTCAGACGGGGC[A/G]GTTGCCAGGCAGAGG	80227
rs190879605	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73905172	GCTTTTTGCAGCTTC[C/T]GGTAAGTCTTAGCTA	80227
rs190885434	snp	C/G	0.0236746	0.106192	intron-variant	PAAF1	GRCh38.p7	11:73900764	GAGGCGGGCGGATCA[C/G]GAGGTCAGGAGATGG	80227
rs190895511	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921435	TCTTTATTATTACTT[A/G]TTCTTACTAAGCGCC	80227
rs191137416	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914239	CTGTGAGTTTTGACA[A/G]ATATATCCAGTTGTA	80227
rs191149745	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892632	TGGGTTTTTACATTA[C/T]ATGCTATTTTATAAC	80227
rs191153038	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73905863	GCATGTATCACTTCC[A/G]TGGAACTCAGTAGCA	80227
rs191154344	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924181	CCACATAGGCCGGGT[A/G]TGGTGGCTCACGCTT	80227
rs191167000	snp	A/C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921541	GAGTTTTTCAAGTAA[A/C/G]GACATGGTCTTCTCT	80227
rs191168858	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879733	AAAAAATTAGTCAGG[C/T]ATAGTGGCATGCGCA	80227
rs191175052	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73898290	CTGAACTCTTGAATC[C/T]TCCTGGTGCATCTTA	80227
rs191388436	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906740	TAAGACTTGAGAGAC[A/G]TGTGGTTAATCACAT	80227
rs191408309	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73883939	TATTTCTAGTTTTTG[A/G]CTATTATGAAGGAAG	80227
rs191426936	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73901999	TTCTCAAGTAGCTGG[A/G]ATCACAGGCGTGCAC	80227
rs191591661	snp	A/T	0.0115144	0.0749975	intron-variant	PAAF1	GRCh38.p7	11:73926413	ATCTATTTCATTTTT[A/T]AAAATTCTTGCGTAG	80227
rs191684756	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73884489	GACAGAGCGAGACCC[C/T]GTCTCAAATATTAAA	80227
rs191696467	snp	C/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73902049	TTGTATTTTTTAGTA[C/G]AGATGGGGTTTCGCT	80227
rs191708588	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919346	TTTGATTGCAGTCCA[A/G]TTTGATAAGGACTAC	80227
rs191708737	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904896	TGAATCTTTTCTTGA[A/G]GGCAAATGCTTTTGT	80227
rs191944225	snp	A/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73896900	CGCCCCTCACCTCCC[A/G]GACGGGGCGGCTGGC	80227
rs191989211	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887970	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT	80227
rs192005320	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73920905	GGTGTAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	80227
rs192039345	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894194	CCGCTCACCTTTTGA[A/G]AAGTAAGTCATTTTA	80227
rs192041383	snp	A/G	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73908490	GCTTACTGTAGCCTT[A/G]AACTCCAGGGCTCAA	80227
rs192197374	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888778	AAGTCTTAGTTAACT[C/G]TGACACTTATTAGCT	80227
rs192221775	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912331	GTCTAACAAGGAGTG[G/T]TTGATCCCTCCCCAC	80227
rs192268545	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910148	GGCTGGCATTGAACT[A/C]CTGGGCTCAAGTGAT	80227
rs192274848	snp	A/C	0.0469222	0.145806	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877077	CCCTCAGGTGAATCC[A/C]GGCCCAGAACAGAGT	80227
rs192289645	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911138	ACACATTATTGTCAC[C/T]CAAAGTTCAGAGTTT	80227
rs192293319	snp	A/G	0.0252325	0.109451	intron-variant	PAAF1	GRCh38.p7	11:73897743	TCCCAGAAGATGGGC[A/G]GCCAGGCAGAGATGC	80227
rs192470848	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888184	AAACTCCATGTATAT[C/T]TTACTTTTACAGCTT	80227
rs192700222	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893529	ATCACCTGAGGTGAG[C/G]AGTTCAAGACCAGCC	80227
rs192716156	snp	C/T			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924981	AGCATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	80227
rs192786990	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917844	CCACTGGACTCCAGC[C/T]TGGGCAACAGAGCGA	80227
rs192832114	snp	C/G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883204	TGGTCTCCAGTGATC[C/G/T]TCCCTCAGCCTCCCA	80227
rs192840454	snp	C/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73916041	CAGTTTGAGCTAACA[C/G]TAAGGAGAAAATAAA	80227
rs192913183	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73908309	TGTGTGTATATATGT[A/G]TATATATGTGTATAT	80227
rs192979061	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73906324	GTGGTGCAATCTCCG[C/T]TCACTTCAACCTCTG	80227
rs193038057	snp	C/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73901711	AAGTAGCTGGGACTA[C/T]GGGTACACGCCCCAC	80227
rs193097428	snp	G/T	0.0532157	0.154195	intron-variant	PAAF1	GRCh38.p7	11:73898037	AAAACACGAAAACCA[G/T]TCAGGCGTGGCGGCG	80227
rs193189087	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889602	TAGGAGAAAAGTACT[A/G]ATTATTGAAATCTGT	80227
rs193251552	snp	C/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73879353	CATCAGAGTGAAAAA[C/G]CTAGTTACTTGACCC	80227
rs193257253	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912113	CTTCTTAAAGGTCTC[C/G]TTTTATGAAACTCCT	80227
rs199543691	in-del	-/G	0.0337553	0.125452	intron-variant	PAAF1	GRCh38.p7	11:73886024	TAAACAGTGTGTTAT[-/G]GGGCTGTTATAGACA	80227
rs199557887	snp	C/G	1.65102e-05	0.00287312	intron-variant	PAAF1	GRCh38.p7	11:73914374	GCACTACCAGCTGAT[C/G]AGCCTCACTGTTATT	80227
rs199668144	in-del	-/T	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73926042	ATATTGCCCTGTGAC[-/T]TTTTTTTTAATTACC	80227
rs199791399	snp	A/G	0.000115625	0.00760258	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887356	TTGTACCATATAGGG[A/G]AACCATCTTTGTATG	80227
rs199794515	in-del	-/AAAC	0.0275645	0.114116	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874988	GAGACTCCATCTCCA[-/AAAC]AAACAAACAAACAAA	80227
rs199993436	snp	A/G			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924651	TCCAGCAAGACTTAG[A/G]CTATGTCACTGAGCT	80227
rs200051596	in-del	-/G	0.150333	0.229274	intron-variant	PAAF1	GRCh38.p7	11:73880686	GCAAGACTCTGTCTC[-/G]GAAAAAAAAAAAAAA	80227
rs200122498	in-del	-/T	0.00953873	0.0683987	intron-variant	PAAF1	GRCh38.p7	11:73894644	AATAATAAAAAAAAA[-/T]CTACTAAAAAAAATA	80227
rs200223301	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73916310	TGGAAAACTGCTACT[A/T]CAGAGTATATTATAT	80227
rs200279777	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913700	ATGAGGGTAAAAAAA[A/G]AAAAAAAAAAAGAAA	80227
rs200366959	in-del	-/TATATATGTG			intron-variant	PAAF1	GRCh38.p7	11:73908330	ATGTGTATATATGTA[-/TATATATGTG]TATATATGTGTATAT	80227
rs200384305	in-del	-/TTTC			intron-variant	PAAF1	GRCh38.p7	11:73883514	TCACTTAGTATAATG[-/TTTC]TTTCTTTCTTTTTTT	80227
rs200387834	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73896255	GAAATATCTGAACTC[-/T]TTTTTTTTTTTTTTA	80227
rs200477261	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73900632	ACACAGTTGGTTTGA[C/T]ACCTAAAGCCTTTTC	80227
rs200566678	in-del	-/AAG			intron-variant	PAAF1	GRCh38.p7	11:73922834	AAAAAAAAAAAAAAA[-/AAG]AAGTTGGATATAGAT	80227
rs200575713	in-del	-/GAGT			intron-variant	PAAF1	GRCh38.p7	11:73901096	GGAAATAGAGAGAGA[-/GAGT]GAGAGAAAAGGAGAT	80227
rs200605106	snp	G/T	0.000921314	0.0214431	intron-variant	PAAF1	GRCh38.p7	11:73916705	GTCTTCTGCAGAGTG[G/T]AAATTTTTATTGGCT	80227
rs200644174	in-del	-/G	0.0185938	0.0946107	intron-variant	PAAF1	GRCh38.p7	11:73891638	AAATTAGCTGAGCGT[-/G]GTGGCACTTACCTGT	80227
rs200676919	snp	C/T	1.64996e-05	0.0028722	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918955	TGAATCCTAGGGCTC[C/T]GGTACAAGTCATCCA	80227
rs200740266	snp	C/T	1.66504e-05	0.0028853	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900401	TAGCTGCGTGGTGAC[C/T]TTCAAAGGTCACAAA	80227
rs200754781	snp	A/T	0.00095533	0.0218347	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909417	TCCTGGATACAGCCA[A/T]CGTTGATCGGGGGAG	80227
rs200800667	in-del	-/TG			intron-variant	PAAF1	GRCh38.p7	11:73908398	GTGTGTATATATATA[-/TG]TGTATATATATGTGT	80227
rs200805659	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73903281	CCCATTCTTCCACAG[C/T]GTGGCAAAAATCAGG	80227
rs200865801	in-del	-/AAT			intron-variant	PAAF1	GRCh38.p7	11:73904740	ATGATAGAGAAACTA[-/AAT]AATAAATACACTTGT	80227
rs200918630	snp	A/G			utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927373	TCTGACTTCTTGGAA[A/G]GAGCAGTCCCGGTTA	80227
rs201021789	snp	A/C	0.000106163	0.00728492	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877075	AGCCCTCAGGTGAAT[A/C]CAGGCCCAGAACAGA	80227
rs201097052	snp	C/T	4.94417e-05	0.00497176	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918984	CACAGATCAGGAGCA[C/T]CAGTTCTATCCCTGC	80227
rs201115285	in-del	-/TT			intron-variant	PAAF1	GRCh38.p7	11:73896296	TTTTTTCTTTTTTTC[-/TT]TTTTATTTATTTTTT	80227
rs201124232	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908339	TATGTATATATATGT[A/G]TATATATGTGTATAT	80227
rs201135154	in-del	-/TA	0.0146672	0.084371	intron-variant	PAAF1	GRCh38.p7	11:73908307	ATGTGTGTATATATG[-/TA]TATATATATGTGTAT	80227
rs201188947	snp	A/C	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73889802	AGCACTCTTGCAGCT[A/C]TATGGGCTTTATCAC	80227
rs201243167	snp	A/G	6.90131e-05	0.00587382	intron-variant	PAAF1	GRCh38.p7	11:73900455	CAAAAGGCTTCTCTA[A/G]TGATCCCCAGAAATG	80227
rs201296473	snp	A/T	6.59924e-05	0.00574385	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878851	ATATATGCTGTGACT[A/T]TAAAGGAGAAGGATT	80227
rs201364777	in-del	-/TT	0.464416	0.128553	intron-variant	PAAF1	GRCh38.p7	11:73900002	AAAGCCATGGAATTC[-/TT]TTTTTTTTTTTTTAA	80227
rs201406236	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888524	CTGGTGAGATGATTC[C/T]GTAAGGGTGGACCAG	80227
rs201497884	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73926115	TTTCTTTCTTTCTTT[-/C]TTTTTTTTGAGATGG	80227
rs201507993	in-del	-/TATATATATG			intron-variant	PAAF1	GRCh38.p7	11:73908389	ATATATATGTGTGTA[-/TATATATATG]TATATATATGTGTAT	80227
rs201521151	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916311	GGAAAACTGCTACTT[C/T]AGAGTATATTATATA	80227
rs201679598	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73882060	GTATTTTTTTTTTTT[-/T]AATAGAGACAGAGTT	80227
rs201696391	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913699	GATGAGGGTAAAAAA[A/G]GAAAAAAAAAAAGAA	80227
rs201699047	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899408	TCTTTTTCTTTTTCT[C/T]TTTTTTTTTTTTTTT	80227
rs201724282	snp	A/G	0.000125243	0.00791237	utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73876997	GAAGGGGCGGAAGAG[A/G]TGGGCTGGTGGAGGC	80227
rs201770537	snp	C/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927358	ACCAGCTTTCTGACC[C/T]CTGACTTCTTGGAAA	80227
rs201817390	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73920932	AGCACTTTGGGAGGC[C/T]AAGGCGGATAGATCA	80227
rs202038064	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73895393	AGCAATTGGATAGAT[-/A]ACCACCTGTATCAGG	80227
rs202040984	in-del	-/A	0.095934	0.196885	intron-variant	PAAF1	GRCh38.p7	11:73879715	ATCTCTATAAAAAAC[-/A]AAAAAAAATTAGTCA	80227
rs202080531	snp	A/C	0.000117699	0.00767046	intron-variant	PAAF1	GRCh38.p7	11:73900427	ACAAAGGAGGTATGA[A/C]GTGTGCTTTCTCCAA	80227
rs202088070	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908389	TATATATATGTGTGT[A/G]TATATATATGTGTAT	80227
rs202208997	in-del	-/CAAA			intron-variant	PAAF1	GRCh38.p7	11:73898812	GGAGTGAAACTCTGT[-/CAAA]CAAACAAACAAACAA	80227
rs367553624	snp	A/G	0.000131833	0.00811782	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914453	CAAAATGCTGCTCTT[A/G]GCCCGGGAAGATAAG	80227
rs367560238	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924513	GGTCTTTGGACCATC[C/T]TCTTTACACTAGTGA	80227
rs367594409	snp	A/G	0.000251896	0.0112198	intron-variant	PAAF1	GRCh38.p7	11:73909350	CTTCTCTGCCCTTGT[A/G]GTTCCTTTACTCCAT	80227
rs367695812	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73885568	CCTCCCGGCCTGGTC[A/G]TGGTGGCTCACACCT	80227
rs367760244	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73919569	AAGAGCACTAGCATT[C/T]CCAGAGGGCCTGCTA	80227
rs367777827	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73880307	ACAAATATATATATA[C/T]ACACACACACATATA	80227
rs367785352	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909718	TCTGTTTTCACCATA[C/T]GATTAATATTTACTC	80227
rs367823995	snp	A/G	0.000693207	0.0186044	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878863	ACTTTAAAGGAGAAG[A/G]ATTAATACCCTTAAA	80227
rs367844659	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899394	CCCATTTGTGTGTTT[C/T]TTTTTCTTTTTCTCT	80227
rs367870596	in-del	-/CTCCTAGAATGGTTA			intron-variant, cds-indel, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888868	GAGATCCTATTCTAC[-/CTCCTAGAATGGTTA]ATGGGGAATGAGACT	80227
rs367879089	in-del	-/A/AA	0.470313	0.216613	intron-variant	PAAF1	GRCh38.p7	11:73913700	TGAGGGTAAAAAAAG[-/A/AA]AAAAAAAAAAAGAAA	80227
rs367938813	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914697	ATTTAAATCCCAGTT[C/T]TTTTTTTTTTTTTTT	80227
rs368002175	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73914697	ATTTAAATCCCAGTT[-/C]TTTTTTTTTTTTTTT	80227
rs368106179	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876499	GGCTTCAGTCTCCTC[C/T]GGAGTAAAATGACGA	80227
rs368380344	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73886182	CAAATTTTACAGGTT[A/G]CTGAAGCTTAATTCT	80227
rs368394522	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913754	GTAGGCCCTAAAGAA[A/G]TATTTGGTGAGTAAA	80227
rs368403454	in-del	-/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876142	AAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAGGTA	80227
rs368538216	snp	C/G	3.57711e-05	0.00422898	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891152	AGGAAAATGCATCTT[C/G]TAAGTTTTTGGCACC	80227
rs368545851	snp	A/G	0.000330589	0.0128524	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924729	ACACCAGACCTGGGT[A/G]ATTCTCATGAGAGAT	80227
rs368549964	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890342	AAATGGCCCTTAGCA[A/G]GTCATGTCTCCTGAA	80227
rs368581380	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73900968	ACCTGGGCGACAGAG[C/G]GAGACTCCGTCTCAA	80227
rs368588922	snp	A/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73918477	CTTTCTCTTTCTTTT[A/T]TTTTTTTATTTTTTT	80227
rs368722847	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886672	AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	80227
rs368764579	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73908857	GCAGTGGCGTGATCT[C/T]GGGTCACTGCAACCT	80227
rs368784455	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73899741	TCGAGAACCTTTCTC[A/G]AGCTCAGTGATTTGG	80227
rs368836618	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73916317	CTGCTACTTCAGAGT[A/C]TATTATATAACCTGC	80227
rs368948648	in-del	-/AT	0.0146672	0.084371	intron-variant	PAAF1	GRCh38.p7	11:73880295	CACACAAATACACAA[-/AT]ATATATATATATACA	80227
rs368998868	snp	A/G	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73905990	ATTCTTAAAAGCTCT[A/G]AGATACTTTCTAATT	80227
rs369047733	snp	A/C/G/T	0.000230614	0.010736	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909486	TTTGGGATTGTGGGC[A/C/G/T]CTCAGCCTGCTTGGG	80227
rs369057155	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73882214	AGAGATGGGGTTTCA[C/G]TGTGTTAGTCAGGAT	80227
rs369147574	snp	C/T	6.60437e-05	0.00574608	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899202	GTCTTCTAGTACTGA[C/T]GGGACCATGAAAATC	80227
rs369208529	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73925465	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs369264165	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73882250	CCATCTCCTGACCTC[A/G]TGATCCGCTCCCTGG	80227
rs369297483	in-del	-/TTAAC			intron-variant	PAAF1	GRCh38.p7	11:73907638	GTGACAGTACCCTAC[-/TTAAC]CTGGTCAACCCCACT	80227
rs369326121	snp	C/G	3.29712e-05	0.00406011	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909406	CTTGCTAGGTATCCT[C/G]GATACAGCCATCGTT	80227
rs369343432	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878347	CCTTTCCATTATACC[C/T]TAAAAGTGCTAGGGT	80227
rs369384306	snp	C/T	0.00676609	0.0577691	intron-variant	PAAF1	GRCh38.p7	11:73881149	GTAATAAACTGTAAC[C/T]AAAAGGCACAGTTTC	80227
rs369416208	snp	C/T	6.94758e-05	0.00589348	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927403	AGTGAAAAGGTTTGA[C/T]CCTGATCAACAATGA	80227
rs369473709	in-del	-/AA	0.00288088	0.0378436	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891195	TTCCAGAATTCATAC[-/AA]AGAGTGTAAGTATTT	80227
rs369612455	snp	A/G	3.29511e-05	0.00405887	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909430	CATCGTTGATCGGGG[A/G]AGGAATGTGGTGTCT	80227
rs369668878	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877904	AAGAAGAAAAGCTGA[C/T]GTCTTAATTAGGAAT	80227
rs369694380	snp	C/G/T	8.45908e-05	0.00650301	intron-variant	PAAF1	GRCh38.p7	11:73899136	CATTGTTTGTTTTCT[C/G/T]TTTGAACAGATAACA	80227
rs369834550	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73914947	CTGACTCAAGTGATC[C/T]GCCTGCCTCAATCTC	80227
rs369844366	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73907083	GTGTATTTTTTCTCT[C/T]TTTTTTTTTCCATTG	80227
rs369849740	snp	A/G	0.0146672	0.084371	intron-variant	PAAF1	GRCh38.p7	11:73897323	CGAGGTGGCTGCCAG[A/G]CGGAGACGCTCCTCA	80227
rs369868262	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927835	CTGGCCATAGAGAAG[A/G]CCTGCTTGGCAGTAG	80227
rs370008556	snp	A/G	4.94572e-05	0.00497254	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878829	CCCCAGGTAATACCC[A/G]TGAATTATATATGCT	80227
rs370041392	snp	A/C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891268	ATTTTATTTGCTTGT[A/C/G]TAGTGCTATAAACAT	80227
rs370121823	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73893792	ACGTGGGCGCGGTGG[C/G]TCATGCTTATAATCC	80227
rs370214827	snp	A/G	1.76886e-05	0.00297389	intron-variant	PAAF1	GRCh38.p7	11:73900223	GGTAAGAGAACATCA[A/G]GGGATGGACAAGAGA	80227
rs370270657	in-del	-/TC	0.00716266	0.059414	intron-variant	PAAF1	GRCh38.p7	11:73921552	GTAAAGACATGGTCT[-/TC]TCTCTTCTGTATAAA	80227
rs370300231	snp	A/G	1.75489e-05	0.00296212	intron-variant	PAAF1	GRCh38.p7	11:73900245	GACAAGAGAACTAGC[A/G]TGGAATTTTCTTTTG	80227
rs370436633	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906577	TTTATTTTAAATTGG[A/G]TCTATTTGAAAAGTT	80227
rs370500568	snp	A/C	0.000115625	0.00760258	intron-variant	PAAF1	GRCh38.p7	11:73914365	GCTGTGTGGGCACTA[A/C]CAGCTGATCAGCCTC	80227
rs370558498	in-del	-/GT			intron-variant	PAAF1	GRCh38.p7	11:73892696	ATGGAGTCTCGCTCT[-/GT]TGCCCAGGCTGGAGT	80227
rs370657879	snp	A/G	4.94678e-05	0.00497307	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918961	CTAGGGCTCCGGTAC[A/G]AGTCATCCACAGATC	80227
rs370660361	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73880224	GCCGTGATCATGCTG[C/T]GTGGTCTCCTACCCT	80227
rs370774390	snp	A/G	1.72937e-05	0.0029405	intron-variant	PAAF1	GRCh38.p7	11:73918899	GTTGAATATAGTCAA[A/G]TATTGCTTTTGAAGA	80227
rs370880256	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73882768	CCACCACGCCCAGCT[A/G]ATTTTTTTGTATTTT	80227
rs370887715	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73905241	TTTCTTTTTTTTTTT[-/T]GAGACAGAATCTCAC	80227
rs370941319	snp	A/G	1.65141e-05	0.00287346	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900325	GGTTTTTCCCATCAG[A/G]CCTTGTGGTCCTGAG	80227
rs370990257	snp	A/G	8.26098e-05	0.00642636	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899175	CATTTCCAGCAGAGG[A/G]GGTCTTGGTGTGTCT	80227
rs371004920	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73908887	TACGCCTCCCAGGTT[C/T]GAGCGATTCTCCTGC	80227
rs371017911	snp	G/T	3.31675e-05	0.00407218	splice-donor-variant	PAAF1	GRCh38.p7	11:73916661	TGTGAGGAGTCCAAG[G/T]TGAGTCACCATTCAT	80227
rs371043533	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917517	TTCAACTGATATTTA[C/T]TGAAAATAGCTTCTG	80227

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