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
rs371045180	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913062	TTGTATTTTTAGTAG[A/G]GATGGGGTTTTGCCA	80227
rs371075483	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73919148	CCATGATTCTTTGGC[-/A]TATTGTACCTATCAA	80227
rs371142167	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73907092	TCTCTTTTTTTTTTT[-/T]CCATTGTAAGTCTTT	80227
rs371293248	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899400	TGTGTGTTTCTTTTT[C/T]TTTTTCTCTTTTTTT	80227
rs371301934	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73879209	CTAGATATTTCTGCT[G/T]AAAGGTCTCACTGTC	80227
rs371370801	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916332	ATATTATATAACCTG[C/T]TCAAGTCCTTAGTCA	80227
rs371376063	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73894644	AATAATAAAAAAAAA[A/T]CTACTAAAAAAAATA	80227
rs371421703	snp	A/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877139	GTCAAGGAGAGCCAT[A/G/T]CCTGGTCCAGGATAT	80227
rs371468192	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73885842	GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	80227
rs371478961	snp	A/C	0.000100746	0.00709666	intron-variant	PAAF1	GRCh38.p7	11:73909354	TCTGCCCTTGTAGTT[A/C]CTTTACTCCATCCTC	80227
rs371480509	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73914722	TTTTTTTTGGAGACA[-/A]GAGTCTCACTCTGTC	80227
rs371598116	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890679	ACTTTTAGACTTGTC[C/T]TTTAAGACCTAGGTT	80227
rs371609866	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73892347	AAAAAAAAAAAGAAA[A/G]AAAGAAAAAGAGCTC	80227
rs371684515	snp	G/T	0.000153988	0.00877327	intron-variant	PAAF1	GRCh38.p7	11:73927243	CTTTTTGAAATGGAA[G/T]AATCCCAGGCTTCCT	80227
rs371684962	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73910208	GACTACAGGCCTGCA[C/T]CACCATGCCTGGCAA	80227
rs371690311	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73927097	GCATCCCAACCATTG[G/T]TGATTGGGATGCATC	80227
rs371717982	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73880348	CTTAACATAAAAATT[C/G]AAGGAAAATACTGTA	80227
rs371746744	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73909998	GTGTTGGGCCTCATT[C/G]AGAGCCACCCTGGGC	80227
rs371747773	in-del	-/GTTT			intron-variant	PAAF1	GRCh38.p7	11:73906269	TTTGTTTGTTTGTTT[-/GTTT]TTTTGAGATTCCCTC	80227
rs371764877	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919751	TGTAGGAATGATGTA[A/G]GTCAGGAGGACTGGA	80227
rs371768448	in-del	-/CTGGA	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73921942	TTTGGAATTGCACTT[-/CTGGA]GTTCCTTCAGACACT	80227
rs371802088	snp	C/G	0.0123036	0.0774623	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876815	GCGGCTTGGGTTTCG[C/G]AGGCGGTTGGGGATC	80227
rs371803408	in-del	-/AAAAAAAAAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73900982	GCGAGACTCCGTCTC[-/AAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	80227
rs371819340	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881699	ACAACCAAGGAGTTT[G/T]TTTGTTTGTTTGTTT	80227
rs371839800	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886826	GAGGTAGGGCCTAAT[G/T]GGGGGTGTTTGGGTC	80227
rs371949979	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73914697	TTTAAATCCCAGTTC[-/T]TTTTTTTTTTTTTTT	80227
rs371999089	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926388	CAGGCGTGAGCCACC[A/G]CGCCCAGCCATCTAT	80227
rs372032974	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894503	AAATCGGAGGGAAGG[A/G]ATAGCATTAGGAGAT	80227
rs372073780	snp	C/G	0.0287284	0.116357	intron-variant	PAAF1	GRCh38.p7	11:73897471	TCACTTCTCAGACGG[C/G]GCGGCCGGGCAGAGA	80227
rs372196275	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73903850	GTACTTTGGGAGGCC[A/G]AGGTGGGAGGATCAC	80227
rs372199415	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73902654	CCTAAGAATATGTAT[-/T]GGACCTTTAGCTTAG	80227
rs372249591	snp	C/T	0.000153988	0.00877327	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909420	TGGATACAGCCATCG[C/T]TGATCGGGGGAGGAA	80227
rs372294739	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73920072	TTTAGGTGGTAGTAG[A/T]GTACCAATATTGGCA	80227
rs372500323	in-del	-/CTCT			intron-variant	PAAF1	GRCh38.p7	11:73926022	CGTAATTGAGACTAT[-/CTCT]ATATATTGCCCTGTG	80227
rs372616132	snp	A/T	1.65373e-05	0.00287548	intron-variant	PAAF1	GRCh38.p7	11:73909602	ATGCCCAGTAAGTTG[A/T]TAATGATATGTAGCA	80227
rs372649193	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73912688	TAAAACTCTCCAGTG[G/T]CCTCCCTTTATAAAT	80227
rs372692899	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73900777	CACGAGGTCAGGAGA[C/T]GGAGACCATCCCGGC	80227
rs372724683	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73922816	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs372732564	snp	C/T	0.000153988	0.00877327	intron-variant	PAAF1	GRCh38.p7	11:73918905	TATAGTCAAGTATTG[C/T]TTTTGAAGAAAGAAA	80227
rs372824046	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878545	ACTGTTGATGGATGA[G/T]CATTAATTTAACCAA	80227
rs372830004	in-del	-/C	0.00654925	0.0568483	intron-variant	PAAF1	GRCh38.p7	11:73883388	AACAGTCACTTTCCA[-/C]CCCCCAATCCTAGCA	80227
rs372928956	snp	C/T	1.8103e-05	0.00300852	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891169	AAGTTTTTGGCACCA[C/T]ATACTACTTTTTCCA	80227
rs372932744	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73911674	TGTTGCCCAGGCTGG[A/C]GTGCAGTGGTGCGAT	80227
rs373003660	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878150	GTGGGCTAAAATACA[A/G]ACTAGTTGCTAGTAC	80227
rs373094916	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73893260	TTCTAATGCATTGCC[A/G]CTTAACTGATGTATA	80227
rs373139313	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73912041	CTCTCCTCAAAAAAC[-/T]TTTTTTTTTCATGGC	80227
rs373155061	snp	A/C/G	0.000132096	0.00812592	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899185	AGAGGAGGTCTTGGT[A/C/G]TGTCTTCTAGTACTG	80227
rs373199616	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73899400	TGTGTGTTTCTTTTT[-/C]TTTTTCTCTTTTTTT	80227
rs373259714	snp	C/G/T	1.70446e-05	0.00291925	intron-variant	PAAF1	GRCh38.p7	11:73916519	TTAATCTTTAAACAG[C/G/T]ATTTTTGCCTCCTAC	80227
rs373309105	snp	C/T	7.19282e-05	0.00599658	intron-variant	PAAF1	GRCh38.p7	11:73899115	AGTATTTCATTATTT[C/T]TAACACATTGTTTGT	80227
rs373378642	snp	G/T	3.29484e-05	0.00405871	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909433	CGTTGATCGGGGGAG[G/T]AATGTGGTGTCTGCT	80227
rs373572986	snp	A/T	1.68778e-05	0.00290493	intron-variant	PAAF1	GRCh38.p7	11:73899249	GAGAACTCAGGGTAA[A/T]GGATTTGGATGTACT	80227
rs373737366	in-del	-/CT			intron-variant	PAAF1	GRCh38.p7	11:73921680	AGGTCTTGAAAGACT[-/CT]AGCATGAACTGTCTC	80227
rs373753555	in-del	-/C	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73922203	GGCATCTTGGTGGCG[-/C]CCGGGTTTCAACCCA	80227
rs373770304	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73900851	GCCGGGCGTAGTGGC[A/G]GGCGCCTGTAGTCCC	80227
rs373821773	snp	C/T	3.31027e-05	0.0040682	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878731	TGTAACTATGGGATC[C/T]TATTCAACTTTGGGT	80227
rs373988543	snp	A/G			downstream-variant-500B	PAAF1	GRCh38.p7	11:73927738	TGGAGGTGCCTGAAT[A/G]TGAAGAACTTTGTTA	80227
rs374027912	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73882266	TGATCCGCTCCCTGG[C/T]CTCCCAAAGTGCTGG	80227
rs374219375	snp	G/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876199	AAAGAGTTCAATAAA[G/T]GATAGTTTTCTCTTC	80227
rs374237947	snp	A/C/G	6.60447e-05	0.00574613	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899203	TCTTCTAGTACTGAC[A/C/G]GGACCATGAAAATCT	80227
rs374298608	snp	A/G	0.000307953	0.0124049	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900384	TGGTCAGCTGAAGAT[A/G]CTAGCTGCGTGGTGA	80227
rs374400300	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73898606	AGAATCACTTGAGCT[C/G]AGGAGTTTGAGACTA	80227
rs374430265	snp	G/T	0.00874735	0.0655527	intron-variant	PAAF1	GRCh38.p7	11:73909093	CGCCCGACCTCTTAA[G/T]TTTTCTTTTTAAAAA	80227
rs374444569	snp	G/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73896141	CTATAAAAGTGAGTT[G/T]GGAAAACAAAAAGTG	80227
rs374447936	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73913481	TTACATTTAAAGTTA[C/G]CCTCCCCATCTAGCC	80227
rs374452064	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884953	CAAGTTCCGCCTCCC[A/G]GGTTCACGCCATTCT	80227
rs374453272	snp	C/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73910944	GCAGTGAGCTGAGAT[C/T]GCTCCATTGCACTCC	80227
rs374470314	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73925560	ATTCATCTGTAAAGA[C/T]AGTAATCTGAAAACT	80227
rs374520072	snp	C/T	0.49681	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73897000	CCCCCACCTCCCTCC[C/T]GGACGGGGCGGCTGG	80227
rs374521546	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906043	GGAGTTGAAATAGAA[A/G]TGTAGATTTTCCAAA	80227
rs374529624	snp	A/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73924174	AATTGGCCCACATAG[A/G]CCGGGTATGGTGGCT	80227
rs374598425	snp	C/T	1.69913e-05	0.00291468	synonymous-codon, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900276	TTTTTCCAGAGAGTA[C/T]TGGAAGGACATGTGT	80227
rs374640159	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921725	TCCACCACTTGCAGC[A/G]TTTATCATTCTGAGG	80227
rs374754858	snp	G/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916579	CAGACGCTTTCAACT[G/T]CTGTACTTTTCTCTC	80227
rs374885062	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921035	CTGGGTGCAGTGGCT[C/T]ACATCTGTTATCCCA	80227
rs374913223	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73893888	ACATAGTAAGACCTC[A/G]TCTCTACAAAAAAAT	80227
rs374942641	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73905819	CCCTGCCTTGAATAC[A/G]TACTTTTCAGAATTT	80227
rs374954956	snp	G/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909509	TGCTTGGGAGTCCTT[G/T]CAGATTGTGGTTCTT	80227
rs375017829	snp	A/G	5.02256e-05	0.00501102	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927371	CCTCTGACTTCTTGG[A/G]AAGAGCAGTCCCGGT	80227
rs375023952	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914330	GCTAACAAAATCAGT[A/C]ATCAACCATCAGTAT	80227
rs375131054	snp	C/T	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73926514	GGAGATTGAGACCAT[C/T]CTGGCCAACACGGTG	80227
rs375133532	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73897549	ATCTCAGACGATGGG[C/T]GGCCGGGCAGAGACG	80227
rs375156920	snp	C/T	0.000164761	0.00907487	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909425	ACAGCCATCGTTGAT[C/T]GGGGGAGGAATGTGG	80227
rs375176783	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73900200	ATATAAGGGACCAGA[A/G]TATGGGAGGTAAGAG	80227
rs375229857	in-del	-/TGCAAC			intron-variant	PAAF1	GRCh38.p7	11:73914784	CTCGGTTCAGCTCAC[-/TGCAAC]CTCCACCTCCTAGGT	80227
rs375318183	snp	C/G	1.71852e-05	0.00293127	intron-variant	PAAF1	GRCh38.p7	11:73899129	TCTAACACATTGTTT[C/G]TTTTCTCTTTGAACA	80227
rs375335179	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73882825	AAGCAGGATGGTCTC[A/G]AACTCCTGACCTTGA	80227
rs375539744	in-del	-/AG			intron-variant	PAAF1	GRCh38.p7	11:73901098	AATAGAGAGAGAGAG[-/AG]TGAGAGAAAAGGAGA	80227
rs375559733	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73885842	AGTGAAACTCCATCT[A/C]AAAAAAAAAAAAAAA	80227
rs375573194	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911373	ATTTTTGTAGAGACA[A/G]GGTCTCACTATGTTG	80227
rs375723537	snp	A/T	0.0158469	0.0875917	intron-variant	PAAF1	GRCh38.p7	11:73916029	GGAAGACATGATCAG[A/T]TTGAGCTAACAGTAA	80227
rs375758223	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73897104	GCTGGCCGGGCAGAG[G/T]GGCTCCTCACTTCCC	80227
rs375837881	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73879797	AGGATCTCTTGAGCC[C/T]GGGAGGTTGAGGCTG	80227
rs375981692	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901990	TGCCTCAGCTTCTCA[A/G]GTAGCTGGGATCACA	80227
rs375986853	snp	A/G	1.6743e-05	0.0028933	intron-variant	PAAF1	GRCh38.p7	11:73909364	TAGTTCCTTTACTCC[A/G]TCCTCCATCTTAGGG	80227
rs376145942	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73882581	CCTCCCAAGTAGCTG[A/G]GATTTCAGACATGCG	80227
rs376222796	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73907947	TGTCCTGTCCAGGAC[A/G]TGTGGGAGGCAATAA	80227
rs376258948	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906519	GACTCCCAAAGTGCT[A/G]GGATTACAGTTGTGA	80227
rs376283946	snp	A/G	0.00010497	0.0072439	intron-variant	PAAF1	GRCh38.p7	11:73900471	TGATCCCCAGAAATG[A/G]ATCACTGAAAAGGTA	80227
rs376323821	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73879690	GGCAACAAAGTGAGA[-/C]CCCCCTCCCCATCTC	80227
rs376353396	snp	A/G	3.36604e-05	0.00410232	intron-variant	PAAF1	GRCh38.p7	11:73899247	TGGAGAACTCAGGGT[A/G]AAGGATTTGGATGTA	80227
rs376410690	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73894501	AAAAATCGGAGGGAA[C/G]GGATAGCATTAGGAG	80227
rs376518385	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893664	ATCGCTTGAACGCGG[A/G]AGGCAGAGGTTGCAG	80227
rs376566257	snp	A/G	0.000118027	0.0076811	splice-donor-variant	PAAF1	GRCh38.p7	11:73891202	ATTCATACAAAGAGT[A/G]TAAGTATTTTGATAA	80227
rs376568654	snp	C/T	1.65299e-05	0.00287483	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900316	ATTGTTGCAGGTTTT[C/T]CCCATCAGGCCTTGT	80227
rs376660007	snp	C/T	1.78976e-05	0.0029914	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891146	GTCCAAAGGAAAATG[C/T]ATCTTCTAAGTTTTT	80227
rs376697233	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73896666	AATTTTTCTTAGTAC[A/G]GAACAAAATGAAAAG	80227
rs376713911	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73905841	TCAGAATTTTTTTTT[-/T]CCAAAAGCATGTATC	80227
rs376974652	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73915969	AAATCAGGTTTTTTT[-/T]GTTTGTTTATTTTGT	80227
rs377033796	in-del	-/CAAA			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875007	AAACAAACAAACAAA[-/CAAA]GTGAAAGAGTGCCCA	80227
rs377108027	snp	A/G	1.6646e-05	0.00288491	intron-variant	PAAF1	GRCh38.p7	11:73909620	ATGATATGTAGCATT[A/G]TTTTATTTTCTTAGG	80227
rs377475132	in-del	-/G	0.00121125	0.0245796	intron-variant	PAAF1	GRCh38.p7	11:73909615	TGATAATGATATGTA[-/G]CATTGTTTTATTTTC	80227
rs377588874	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902113	GTGATCTGCCTACCT[C/T]GGCCTCCCAAAGTGC	80227
rs377632289	in-del	-/C	0.49423	0.0534032	intron-variant	PAAF1	GRCh38.p7	11:73897237	CGGGCGGGGGGCTGA[-/C]CCCCCCCACCTCCCT	80227
rs377635141	snp	A/T	0.000153988	0.00877327	intron-variant	PAAF1	GRCh38.p7	11:73914551	GAGGCAACCTGGGTC[A/T]CTCTGTGTCTTAGAA	80227
rs377643028	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73898641	GGGCAACATGGTGAA[A/G]CTCTGTCTCTACCGA	80227
rs377643711	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918537	GTTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	80227
rs377645343	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879922	ATAAAGGATGGACTT[C/T]ATAGTGCTGTGACTT	80227
rs377654398	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73922703	GCGCCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG	80227
rs377667435	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73920966	GAGGCCTTGATATTT[C/G]TCGCCTCCTCTGTCC	80227
rs377670122	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73902195	ATTTCTTTATAACAT[G/T]TTGCCAGATTACATG	80227
rs377733465	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73882311	GCACCGTGCCTGCAC[-/T]TTTTTTTTTTTTTTT	80227
rs386754962	multinucleotide-polymorphism	AG/GT			intron-variant	PAAF1	GRCh38.p7	11:73885627	TGGGTGGATCACCTG[AG/GT]GGGAGGAGCTCAAGA	80227
rs397748911	in-del	-/A	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73879723	AAAAAACAAAAAAAA[-/A]TTAGTCAGGCATAGT	80227
rs397838726	in-del	-/AGAG			intron-variant	PAAF1	GRCh38.p7	11:73901095	GGGAAATAGAGAGAG[-/AGAG]TGAGAGAAAAGGAGA	80227
rs398016652	in-del	-/T	0	0	intron-variant	PAAF1	GRCh38.p7	11:73921314	ACCTTGCAACAGAGA[-/T]TTTTTTTTTTTTTTG	80227
rs398045269	in-del	-/A	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73879884	CATTAAAAAAAAAAA[-/A]GACTATTGTTTATAT	80227
rs398045270	in-del	-/TT	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73901888	TTTTTTTTTTTTTTT[-/TT]AGTTTCGCTTGTTGC	80227
rs398045271	in-del	-/A	0.5	0	intron-variant	PAAF1	GRCh38.p7	11:73911011	AAAAAAAAAAAAAAA[-/A]GTACAGGGAGTTCTT	80227
rs527255019	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906906	ACTCTTAATTTATTG[G/T]GCACCTATACTAAGC	80227
rs527374786	snp	A/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921573	TTCTGTATAAAACTT[A/T]ATGAAATAAAGGCAA	80227
rs527463509	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927472	TTAATGTCTTGGGCA[C/T]CCCTTGGAAATCACA	80227
rs527536789	snp	A/C	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73884293	TTGCTTGAGCCCAGC[A/C]GTTCGAGACCAGTCT	80227
rs527613308	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73884778	GGGATTTATCCCTCA[A/G]CTATCATTTCCATGA	80227
rs527624856	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877482	GCTATATTAGGCATA[C/T]TGGACGATACTATTA	80227
rs527766166	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906247	TATAAATTGAATTTC[A/G]TTTAGTTTTGTTTGT	80227
rs527850540	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73911758	TGTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	80227
rs527896798	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890570	CCTACATATTTTATG[A/G]GTGTACCATAATTTA	80227
rs527912511	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912542	CTCTCCCTTCCTCCT[A/G]TCAACATCTGGTCCA	80227
rs527945936	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, splice-donor-variant, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876742	CTCCTGAAGAACGCG[C/G]TACGCGATGCTCACC	80227
rs527984762	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919440	GGTCTTCGTGAACTA[C/T]GTGACATGTAAACTG	80227
rs528085865	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888749	CTATGGGTATTATAG[A/G]TATCAGAAGATCTAA	80227
rs528147180	in-del	-/AT			intron-variant	PAAF1	GRCh38.p7	11:73908372	TGTGTATATATATAT[-/AT]GTATATATATGTGTG	80227
rs528236677	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896626	GGGGGTAAGGTCACC[C/G]ATCAACAGGATCCCA	80227
rs528447365	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922319	GGAGTAAGATTATAA[C/T]TCTGTTTTCAGAGGA	80227
rs528473113	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880318	TATATACACACACAC[A/T]TATACATATGTATAC	80227
rs528658196	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914590	TGGAAACATTTCTAC[C/T]TGCTCCCTGTGTTCA	80227
rs528695338	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894872	GCCTGTAGTCCCAGC[C/T]GCTCGAGAGGCTGGG	80227
rs528831434	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73894098	ATAAGCCACTGTGCC[G/T]GGCCTTTATACATCA	80227
rs528864743	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73895959	AAAAAAAAGTTAAAA[A/G]ATTAGCTGGACATGC	80227
rs528965058	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901807	ACTCTTGACCTCAGG[G/T]TGATCCACCAGCCTC	80227
rs529024412	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73885107	CTCGTGATCCACCCG[C/T]CTCGGCCTCCCAAAG	80227
rs529097205	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73908243	TATGTGTGTATATAT[A/G]TGTGTATATATATGT	80227
rs529123676	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915804	CTTTAGTGATTTGAT[G/T]TGGCCACAGGGTTTG	80227
rs529198891	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922227	CAACCCAGAGGAGCA[G/T]ATTTTTTGTACTTTT	80227
rs529254837	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73878966	CTGTATGGCCAACAC[C/T]CCAACTCCTCCATTC	80227
rs529277101	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875496	AGACTGGGACCACAG[C/T]GGAGGGATGCCTAAT	80227
rs529280852	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886477	TCAGGAGATCGAGTC[C/T]ATTCTGGCTAACATG	80227
rs529374946	snp	A/G/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73894008	GAGTCCTGCTCTGTT[A/G/T]CCCAGGCTGGTCTCA	80227
rs529398116	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885907	ATTTCTGCTTCTCTC[C/T]TGTAACTTCAGTTTG	80227
rs529514523	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900708	TGTTTTCTGGCCGGG[C/T]GCGGTGGCTCACGCC	80227
rs529516315	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893398	TAATTAAATCTTATG[A/T]TAAATCAATAAAATG	80227
rs529539893	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73906773	GATTGGCACTTGTAC[A/G]TTACGCTGAGTTGCT	80227
rs529630921	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899042	GGGAAACACAGGCTT[C/T]AGGAAGTCTTGGAAG	80227
rs529655963	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73899965	CACCTCAGCTCTTTA[A/G]CTAGATCTAGAGATG	80227
rs529673802	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876098	CGCCACTGCATTCCA[C/G]CCTGGGTTACAGCGG	80227
rs529784822	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890629	ATGTCAGTAGTCTAA[C/T]ATTCTCTCTAAAAGT	80227
rs529964126	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73900855	GGCGTAGTGGCGGGC[G/T]CCTGTAGTCCCAGCT	80227
rs529982739	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903532	GACCAGCCTGGCCAA[A/C]ATGGTGAAACCCAGT	80227
rs529989459	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904309	AAATGCACTTTAATC[A/G]GTTTGAAGTTAAATT	80227
rs529998118	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917495	CTCCTTTGATTTCCT[C/T]CCTTTTTTCAACTGA	80227
rs529999547	snp	A/G	0.000115334	0.00759299	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909419	CTGGATACAGCCATC[A/G]TTGATCGGGGGAGGA	80227
rs530057118	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910046	TGCTTTAAAACATTT[A/G]GAGAACAGTAACATT	80227
rs530062483	snp	C/G	0.0539704	0.155153	intron-variant	PAAF1	GRCh38.p7	11:73896972	GGCGGCTGGCCGGGC[C/G]GGGGGGCTGACCCCC	80227
rs530070604	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874793	AAGTTCAAGACCAGC[C/T]TGGCCGGGATGATGA	80227
rs530144041	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875155	CAAAAATGTGAGGTG[C/T]ATTTATTTGCCCAAA	80227
rs530249643	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73895060	AAAGATGATTCATCC[A/G]TTTATTAATCACCTA	80227
rs530267191	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923628	GCAACCTCTGCTTCC[C/T]GGGTTCAAGCGATTC	80227
rs530296345	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881121	TTATTATTACAAGGA[A/C]CTTGGCTATCTTGTA	80227
rs530296907	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888746	CAGCTATGGGTATTA[C/T]AGGTATCAGAAGATC	80227
rs530357250	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888639	TACTTTGTTTTTTAC[A/G]TAAGATTTTTAGCAA	80227
rs530486914	snp	G/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73880418	AAATCCTATTCTAAC[G/T]GCTTGAGCTAGGATT	80227
rs530512237	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881814	TGGGTTCAAGCAATT[A/C]TCCAGCCTCAGCCTC	80227
rs530726165	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73903482	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	80227
rs530730088	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896713	CTTTCTACACAGACA[C/T]GGCAACCATCCGATT	80227
rs530759958	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881443	GCTGGGACTACTACC[A/G]TGCCCAGCTAATTTT	80227
rs530869114	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902850	TACAGGCATGCGCCA[C/T]CATGCCCGGCTAATT	80227
rs530899439	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922944	AAATTTTTTGATGCA[A/G]ATTGCCAAACATATC	80227
rs530920856	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880860	AAAAAATTACCTGGG[C/T]GTGGTGGTGCATGCC	80227
rs531014368	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73910333	TTGAACCTTTAGAGG[A/G]TAAGTTGAAGTTGAA	80227
rs531074958	in-del	-/AAAC			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874989	GAGACTCCATCTCCA[-/AAAC]AAACAAACAAACAAA	80227
rs531075936	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902127	TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTA	80227
rs531077537	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73895000	AAAACAAACATAACT[C/G]TGCTCCTTTTCTATT	80227
rs531095788	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73879864	GGTGACAGAGTGAGA[C/T]CCCATCATTAAAAAA	80227
rs531121817	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887481	TTATGTCTTCTAGAT[A/G]GCATGATATTTAAAA	80227
rs531134444	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73883547	TTTTGAGAGTCTCAC[C/T]GTGTCGTCTAGGCTG	80227
rs531137334	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886908	GTGACTGAGTTCTCA[C/T]TCTGTTCTTTCCTGA	80227
rs531160652	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920956	TAGATCACCTGAGGC[C/T]TTGATATTTCTCGCC	80227
rs531262372	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917590	AAGGTACAGGCTCTG[A/G]GCTGGGCGTGGTGGC	80227
rs531294460	snp	A/G	0.00013231	0.0081325	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927340	ACGGTCTTGTACGAC[A/G]CTACCAGCTTTCTGA	80227
rs531296795	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912767	TTTCTGACCCCTACA[C/T]TTCTCTCCAGTCTCA	80227
rs531303891	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920306	TGGGAGGCTGAGGCG[A/G]GAGGATCACTTGAGC	80227
rs531338445	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73889547	TATCTTCCTTTGTAG[A/T]CTGTTTGTGGATTAA	80227
rs531428293	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73895517	TTAGAAAATGTTAGA[A/G]TTGATGGATATATCC	80227
rs531438426	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73926681	GTCACTGCACTCCAG[C/T]CTGAGCGACGGAGCA	80227
rs531494318	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73896920	GGGCGGCTGGCCGGA[C/T]GGGGGGGCTGACCCC	80227
rs531528827	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73892266	AGGTTGAGGCTGCAG[G/T]GAGCCATGATCATGC	80227
rs531545505	snp	A/C			intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919275	GAATTTAGCTCAATG[A/C]CCACCACTCTTCTGC	80227
rs531557142	in-del	-/A	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73921598	AGGCAAAAGATTCGT[-/A]TATCTTGCTGGAAAA	80227
rs531588087	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890808	ATTTTCTTCTTAAAA[C/T]GAATGCTCTAATGCT	80227
rs531600096	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898076	CAATTGCAGGCACTC[A/G]GCAAGCTGAGGCAGG	80227
rs531691877	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911708	TTGGCTCACTGCAGC[C/T]TCCACCTCCCAGGTT	80227
rs531809646	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904624	AGTAATAGGAGGTGC[G/T]TCAAGGCTTATTTTT	80227
rs531810825	in-del	-/A	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73881588	CACTGCCCCCGGCCT[-/A]AAAACAGTTTTAAAA	80227
rs531845247	in-del	-/T	0.240478	0.249819	intron-variant	PAAF1	GRCh38.p7	11:73921393	TTCTACTTTTTGTAC[-/T]TTTTTTTTTTTGGAA	80227
rs531858345	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875374	CCAGGCACTATGCTA[C/G]TGCTGAGGATTCAAG	80227
rs531883236	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882516	CAGTGGTGCGATCTC[C/T]GCTCACTGCAACCTC	80227
rs531892649	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875900	AAATGGGCTTTGAAA[C/G]AGACTTGGACCTAGC	80227
rs531893997	snp	A/T	0.000410762	0.0143252	intron-variant	PAAF1	GRCh38.p7	11:73918485	TTCTTTTTTTTTTTT[A/T]TTTTTTTTTGAGATG	80227
rs531987970	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919504	GACACTGAAAGCTGA[A/G]GCTATTGTATATGCA	80227
rs532007200	in-del	-/AGG	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73882224	TTCACTGTGTTAGTC[-/AGG]AGGATGGTCTCCATC	80227
rs532071084	snp	A/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73926187	TCTCAGCCCACAGCA[A/T]CCTCCGCCTCCCAGG	80227
rs532122664	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877216	GGTCCGGAAAAAGAA[A/G]TATCAAACCCGTATG	80227
rs532218204	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73891433	AGATTATATGAAATT[C/T]CCTTACATATGTTTT	80227
rs532228420	snp	G/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875403	AGACTGTCTAAGTCA[G/T]TTAAGTTCCTGGCTT	80227
rs532305709	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73897119	TGGCTCCTCACTTCC[C/T]AGTAGGGGCGGCCGG	80227
rs532508160	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903806	TAAAAAAAATTGGCC[A/G]GGCGCAGCGTCTCAC	80227
rs532619735	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881159	GTAACCAAAAGGCAC[A/G]GTTTCTTTAAAGCAA	80227
rs532667103	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889409	ATTTTATCTTAGTGC[A/G]GCATACTCACACTTT	80227
rs532673779	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890897	AAGATAATGGCATCT[C/T]AGCAATACCAAATTA	80227
rs532685325	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923704	CCATGCTCGGCTAAT[G/T]TTTTTTGTATTTTTA	80227
rs532706321	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881769	TGGAGTGCAGTGGTG[C/G]AATCTTGGCTCACTG	80227
rs532757084	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73917552	CATCAGGCTTGGTTC[A/G]AGGCACTGAAAACCA	80227
rs532766028	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901714	TAGCTGGGACTACGG[A/G]TACACGCCCCACACC	80227
rs532838816	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907504	TTGCCTTCTAGTGGC[A/G]TTATAAGCTTGGTTC	80227
rs533158371	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913607	TTCACTAGAATCCTT[A/G]AGAGTGAGGACCTTA	80227
rs533161164	snp	C/G	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73884863	TGACTTTCTTTTATT[C/G]TTTTTTTTTTTTTTG	80227
rs533164026	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902566	GTGCACATCCAGTTT[A/G]TAAATACCTTTGGAT	80227
rs533229652	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73885726	ACGTGCCTTTAATCC[C/T]AGGTACTTGGGAGGC	80227
rs533244040	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921151	CTAAAAATACCAATA[C/T]TAGCTAGGCATGGTG	80227
rs533282792	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73907740	GCCCCACTGAAACCA[C/T]GGGGGAGGGGAAGTA	80227
rs533349660	snp	C/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73893817	TAATCCCAGCACTTA[C/G]GGAGACCCAGAAAGG	80227
rs533362990	snp	A/G/T			intron-variant	PAAF1	GRCh38.p7	11:73904688	CCCATATACGCATGT[A/G/T]TGTATATTGCTCCCT	80227
rs533391519	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927589	GTTCCAACTTCTCCT[C/T]GTATAAACTCACCCC	80227
rs533438430	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912745	GGTTTACAACAAGCT[C/G]TTATACTTTCTGACC	80227
rs533500047	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876143	AAAAAAAAAAAAAAG[A/G]AAAAAAAAAAGGTAA	80227
rs533568855	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899005	TAACTCAACCTTTAC[A/C]TCAAACACAAGTCCT	80227
rs533771568	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912849	TTTCTTCTTTCAGTA[C/G]AGTAGACTCTCCCAG	80227
rs533794673	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892819	GCCTGCCACCACGCC[C/T]GGCTAATTTTTTTTG	80227
rs533961055	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920516	CCCTGGGTGACAAAG[C/T]GAGACTCTGTCTCAA	80227
rs533977386	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891365	TGTTTGGCAAAACTG[A/G]TACTCTAGTCCACAT	80227
rs534013820	snp	A/C	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73890876	AGCAGCTTATTTCAA[A/C]ACAAAAAGATAATGG	80227
rs534072772	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73891639	AATTAGCTGAGCGTG[C/G]TGGCACTTACCTGTA	80227
rs534213102	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876470	GCTGCTGTACTCTCC[C/T]CTCACCACCTTTTGG	80227
rs534342122	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73885200	CTGGAGTGCAATGGC[A/G]TGGTCTCGGCTCACT	80227
rs534401479	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887181	AAACAGACTAAGACA[A/C]CTAATCTAATTCTCT	80227
rs534436921	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879930	TGGACTTTATAGTGC[C/T]GTGACTTGCCAATCA	80227
rs534494944	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73911142	ATTATTGTCACCCAA[A/G]GTTCAGAGTTTACAT	80227
rs534645379	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73923091	ATTTTGAAATATATC[A/G]TGAGCGTCTTATTTC	80227
rs534842621	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895475	CAGTCCTTTTATTCC[A/G]AGGAAGCAAAATGAA	80227
rs534910737	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876822	GGGTTTCGCAGGCGG[C/T]TGGGGATCCTCTGTA	80227
rs535031370	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907676	TAGGGGAATGGGAGT[G/T]CTGCTGCCGGCTTCC	80227
rs535110838	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921891	AATGGGAAAGTTAGT[G/T]ATTCCCAGTGTATAC	80227
rs535161372	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894394	CCTGTAATCCCATCA[C/G]TTTGGGAGGCTGGGG	80227
rs535217604	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895237	AAAAAATTTTGGCCT[A/G]AGAAGTAGGTGAATT	80227
rs535217832	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886134	AGTATCTTACTTAGC[C/T]CATATCTCTGCAAAA	80227
rs535234384	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899678	TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT	80227
rs535288959	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73907508	CTTCTAGTGGCGTTA[C/T]AAGCTTGGTTCCCTG	80227
rs535304975	in-del	-/AAAC			intron-variant	PAAF1	GRCh38.p7	11:73926712	AGAGTCTGTCTCAAA[-/AAAC]AAACAAACAAAATTC	80227
rs535312662	snp	C/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73893598	AAAAATTAGCCAGGC[C/G]TGGTGGCGTGCACCT	80227
rs535361045	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916957	TTTAATTTTAAAGAG[C/T]TCAGTAATTTTCTCT	80227
rs535380411	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907122	TATGTCTATAATCAA[C/G]TCTATTTTTTTATGC	80227
rs535428239	in-del	-/TGTATATATG			intron-variant	PAAF1	GRCh38.p7	11:73908256	ATATGTGTATATATA[-/TGTATATATG]TGTATATATGTGTAT	80227
rs535594811	snp	A/C	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73907648	CCTACTTAACCTGGT[A/C]AACCCCACTGGGTAG	80227
rs535747200	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73914658	GTAATGATTAAGAGT[C/T]GTGGGATTTGGAATA	80227
rs535823980	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73921365	AGTGTAGGTGGAGAA[G/T]AGCTGACTCATGGTT	80227
rs535833069	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875776	TGTAGGACATAGTAG[A/G]GAGTTTAAGACTTTT	80227
rs535845341	snp	C/T	0.084728	0.187577	intron-variant	PAAF1	GRCh38.p7	11:73897276	GGGCGGCTGGCCGTG[C/T]GGGGGGCTGACCCCC	80227
rs535852144	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73927151	TGTAAGCACATAATT[A/T]TGGATGTAATTCTGT	80227
rs535909127	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73896100	AGCAACAGAGTGAGA[A/C]CCTGTCTTTAAAAAA	80227
rs535911442	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885069	TTTCACCGTTTTAGC[C/T]GGGATGGTCTCGATC	80227
rs535922082	snp	A/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73881883	GGCTAATTTTTTGTA[A/T]TTTTTTTTGAGATGG	80227
rs535964442	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920818	GAGCACGCCACTGCA[C/T]TCCAGCCTGGGTGAC	80227
rs536075502	snp	A/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925041	ATGCCTGTAGTTCCA[A/G]TTACTTGGGAGGCTG	80227
rs536208609	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73919132	GTTGGGGCATGGTCC[C/T]CCATGATTCTTTGGC	80227
rs536217644	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878056	TTTCAAATTGAAACA[A/G]TGGTGAAGATGAATG	80227
rs536269821	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73902965	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG	80227
rs536288917	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73910514	AGGAAATGGGTTGAA[C/T]AGCTGTGGTGAGAGA	80227
rs536298140	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874844	TACAAAAATTAGGCG[A/G]GCGTGATGGCAGGCA	80227
rs536360537	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917201	AATTTTTGTATATTT[A/T]GTAGAGACAGGGTTT	80227
rs536417624	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915619	GTCTCAAAAAAGGGA[C/G]TCATGCATTCAGGAC	80227
rs536417737	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922986	AGAATGGCACGATGA[A/G]CCTGTTATACCCATT	80227
rs536425541	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894095	GGTATAAGCCACTGT[A/G]CCTGGCCTTTATACA	80227
rs536463540	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881288	TTGCCGATACATACT[A/G]TTAAAGCAGTATTTT	80227
rs536483108	snp	A/G	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73908341	TGTATATATATGTGT[A/G]TATATGTGTATATAT	80227
rs536484845	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917350	AGTTCAAGGAACCCA[C/G]CTCTGTTAGTTATGT	80227
rs536485933	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916291	TGTGTTGAGTGGTAG[C/T]AGTTGGAAAACTGCT	80227
rs536535035	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73896725	ACACGGCAACCATCC[A/G]ATTCTCAATCTTTTC	80227
rs536556504	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73922512	TGTAGAGGGAGTTCT[G/T]TACTGGTTTAGAAGT	80227
rs536684710	snp	C/T	1.65151e-05	0.00287355	intron-variant	PAAF1	GRCh38.p7	11:73909393	GGAGTTTTTTTCTCT[C/T]GCTAGGTATCCTGGA	80227
rs536713575	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888866	CTGAGATCCTATTCT[A/G]CCTCCTAGAATGGTT	80227
rs536786786	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876638	CAGCCACGAGGCCTG[A/G]GGCGCCTCAGGCGTA	80227
rs536792355	snp	G/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73881260	ATCTTTTCCCTAATA[G/T]TTTGCATTTTTCTTG	80227
rs536831627	snp	C/G			utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927602	CTTGTATAAACTCAC[C/G]CCAGCAACACAGGGC	80227
rs536906650	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879827	GCAGTGAGTTATGAT[A/C]GAACCATTGCACTTT	80227
rs537084531	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917060	GAGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC	80227
rs537107185	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880618	AGTGAACCCGGGAGG[C/T]GGGGCTTGCAGTGAG	80227
rs537212783	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921923	TTTCTTTCTCACCTT[A/G]GCTTTTGGAATTGCA	80227
rs537273780	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914778	CGCAATCTCGGTTCA[A/G]CTCACTGCAACCTCC	80227
rs537316650	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73920038	AAGGAAAGACTGGTG[-/A]AAAAAAAAAAGCATG	80227
rs537321907	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73895722	ATTTGCAGCTGGTTG[C/T]TTTTTAATAAAAGTG	80227
rs537407209	snp	A/G/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73908317	TATATGTATATATAT[A/G/T]TGTATATATGTATAT	80227
rs537453025	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914287	AGATACAGAACATAA[C/T]AAATGTTTTCTTTGT	80227
rs537540697	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912047	TTTTTTTTTTCATGG[C/T]TTCTGTGATACCACA	80227
rs537541517	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73915564	AGTGAGCCAAGATTG[C/T]GCCACTGTACTCCAG	80227
rs537623318	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926351	CTGAGGCCTGCCTCA[A/G]CCTCCCAAAGTGCTC	80227
rs537623372	snp	C/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73918807	CAGTTAAGGTTCTTG[C/G]CAGGAAAGAAACCAT	80227
rs537633247	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880689	AAGACTCTGTCTCGA[A/G]AAAAAAAAAAAAAAA	80227
rs537646982	snp	G/T	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73897680	GCGGCCGGGCAGAGA[G/T]GCTCCTCACTTTCCA	80227
rs537685044	snp	G/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73919637	TCTAGGTAAAGCGAG[G/T]ATCTTAATGTAGCCA	80227
rs537701053	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878637	GTCTTAGAATGATCT[A/G]TACTCGATGAGAGGT	80227
rs537706548	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882759	AGGTGTCCGCCACCA[C/T]GCCCAGCTAATTTTT	80227
rs537715051	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886116	TGTGTTTATGTGTAG[A/G]ATAGTATCTTACTTA	80227
rs537737918	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73915033	CTTGTGCAGCACTTG[C/T]AGAGAATAAAAAAAT	80227
rs537757659	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73925585	AAAACTCTTTGTAAA[C/T]ACATTCTATAAATAT	80227
rs537857137	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890802	TATTAGATTTTCTTC[G/T]TAAAACGAATGCTCT	80227
rs537868463	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906399	CTGGGATTACAGGCA[A/C]CTGCCACCACACCTG	80227
rs537928363	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73897132	CCCAGTAGGGGCGGC[C/T]GGGCAGAGGCGCCCC	80227
rs537985153	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886566	GTAGTCCCAGCTGTT[C/T]GGAGGCTGAAGCAGG	80227
rs537992123	snp	A/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73897620	CTCCTCACTTCCTAG[A/T]TGGGATGGCGGCCGG	80227
rs538077319	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911413	GTGTTGAACTCATGG[C/T]CTCAAGTGATTCTCC	80227
rs538147777	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73917681	GTTCAAGACCAGCCT[A/G]GCCAACATGGCGAAA	80227
rs538189189	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876335	AATCCCAGCACTACG[C/T]CTTACTATGTAATCT	80227
rs538234818	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73922589	TTCGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	80227
rs538258201	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73882073	TTTAATAGAGACAGA[A/G]TTTCTCCATGTTGGT	80227
rs538314507	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73916940	ATTGATTGTCTAGAA[C/G]TTTTAATTTTAAAGA	80227
rs538349523	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918682	GTTTAACATACTGCT[A/G]ATATTGTTATCTTCA	80227
rs538373571	snp	A/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888587	TAAACTTTTTAGTTA[A/T]AAAAAATATTTTGGG	80227
rs538378734	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890161	CAGCTCCTCAGTTCC[A/T]TATAGGAGATCTATA	80227
rs538486699	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73925401	GGCCTGGGAAGTTGA[A/G]GCTGCAGTGAGCTGT	80227
rs538519945	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889909	GTTTGTGTAGATAGT[C/T]TAATTGTCATTTTAA	80227
rs538602486	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884360	AAAATAAAAAAAATA[A/G]CTGGGCATGGTGGCA	80227
rs538656885	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73897017	GACGGGGCGGCTGGC[C/G]GGGCAGAGGGGCTCC	80227
rs538725285	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902994	TGAGCCACTGCGCCC[A/G]GCCTAGAATGTTAAA	80227
rs538731710	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73910599	TGCATCTCTGTTCCA[C/T]AGGACAATGTTTTTT	80227
rs538799281	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908891	CCTCCCAGGTTCGAG[C/G]GATTCTCCTGCCTCA	80227
rs538828654	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914663	GATTAAGAGTTGTGG[A/G]ATTTGGAATAAGGGC	80227
rs538853416	snp	A/G	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73917858	CCTGGGCAACAGAGC[A/G]AGACTCTATCTCAAA	80227
rs538860653	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73902595	ATCACTGCAATTATT[C/G]TTCCCTTTACAGAAT	80227
rs538860940	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909496	TGGGCGCTCAGCCTG[C/T]TTGGGAGTCCTTGCA	80227
rs539084700	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927867	AATAAATGTCCTGTA[A/C]GCTGCCACCTGGGAG	80227
rs539161585	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73896827	GTACACCTCCCAGAC[G/T]GGGTGGTGGCCGGGC	80227
rs539185760	snp	G/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73900834	AAAAATACAAAAAAT[G/T]AGCCGGGCGTAGTGG	80227
rs539341430	snp	A/C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913002	CCGCCTCAGCCTCCC[A/C/G]AGTAACTGGGATTAC	80227
rs539342564	in-del	-/TA	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73904097	CAAAAAAAAAAAAAG[-/TA]TATATATATATACAT	80227
rs539420373	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73894167	ATTCACCTCTTGGGA[A/G]AGTTGGGAATGCCGC	80227
rs539435873	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877531	CCAGGCCCCATACTG[A/G]ATGCTTGGTGGAGCT	80227
rs539443954	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904580	CCAAGTCTTAAATAC[G/T]TTCTTAGAAATTGGC	80227
rs539591671	snp	G/T	0.000399281	0.0141238	splice-donor-variant, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877069	GGCGCAAGCCCTCAG[G/T]TGAATCCAGGCCCAG	80227
rs539628785	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886983	TTACTTCCTCTCTCA[C/T]CATGTGATCTCTGCA	80227
rs539646849	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891836	TGCTCATATTTTATT[C/T]CTTTTCCTATAGGAC	80227
rs539784287	snp	A/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73898390	TATATTTACTTTAAA[A/T]TTTTTTGTAGAGATG	80227
rs539785570	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920029	CAGGATGTTAAGGAA[A/G]GACTGGTGAAAAAAA	80227
rs539827001	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73901838	GGCCTCCCAAAGTGC[C/T]GGGATAACAGGCATT	80227
rs539890657	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73926630	AGGAGAATGGCGTGA[A/G]CCCGGGAGGCGGAGC	80227
rs539972390	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884317	CCAGTCTGAGCAACA[C/T]AGTGAGACTCTGTCT	80227
rs540069027	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73898009	AACACAGCGAATCCC[C/T]GTCTCCACCAAAAAA	80227
rs540103100	snp	C/T	0.00914312	0.0669923	intron-variant	PAAF1	GRCh38.p7	11:73897910	TGAGCACTGAGTGAA[C/T]GAGACTCCGTCTGCA	80227
rs540113967	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905472	TGTGATCCTCCCTCA[C/T]TGGCCTCCCAAAGTG	80227
rs540143230	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73902237	GCAAACACACACATT[A/G]ACCTAAGTACATAAA	80227
rs540260241	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919176	CAATAGTGTTTATCA[C/T]TCTACGTTGTGATTG	80227
rs540270550	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884612	TGGTAAACACAATAG[A/G]GAATCATGGAGTGGG	80227
rs540272384	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908399	TGTGTATATATATAT[A/G]TGTATATATATGTGT	80227
rs540318817	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73882340	TTTTTGAAGGTAACT[G/T]GTAGATTCAGTTTTC	80227
rs540331433	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73880892	GTAATCCCAGCTACT[C/T]GGAAGGCTGAGGCAG	80227
rs540400247	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875777	GTAGGACATAGTAGG[A/G]AGTTTAAGACTTTTT	80227
rs540429213	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881646	CAAACTTAATGTTGT[C/T]GTTGTTGTTGTTGTT	80227
rs540569272	snp	C/G/T	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73926465	CTCATGCCCAGCACT[C/G/T]TGGGAGGCGGAGGGG	80227
rs540570081	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73896923	CGGCTGGCCGGACGG[C/G]GGGGCTGACCCCCCA	80227
rs540686683	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879412	ATCAATTTTTCTTTT[G/T]AACAACAGTCTTATA	80227
rs540701633	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915698	CCTCTGAATTTTTGC[A/T]GGGCAGATTATGTTC	80227
rs540711749	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875169	GTATTTATTTGCCCA[A/G]ACTGTCTTGCCCGTC	80227
rs540852483	snp	C/G/T	6.597e-05	0.00574293	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878774	GCTTTTGTCTTTCTT[C/G/T]GTAGGAAGGATGAAG	80227
rs540907201	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921620	GCTGGAAAATGCTGC[C/T]CAGGGCTCTGGAGAT	80227
rs540942505	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73925722	TTTATATACGTTATC[G/T]CATGTAATCTTTGTT	80227
rs541019776	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73899687	AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCG	80227
rs541121559	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73922126	ATTGACTTCTGATAG[A/G]TAACAGTGCCATGTT	80227
rs541302821	in-del	-/TGTT	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73889549	TCTTCCTTTGTAGTC[-/TGTT]TGTGGATTAAAGATT	80227
rs541350203	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877175	GGGGTTACTTCGTCA[A/G]TTGTCGAGGGATATG	80227
rs541366746	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920267	GGCTGGGCACAGTGG[C/T]TCATGCCTATAATCC	80227
rs541389421	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907149	ATGCTGTGTATTCCT[C/G]AGGCTAGGGACCATA	80227
rs541408574	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921547	TTCAAGTAAAGACAT[A/G]GTCTTCTCTCTTCTG	80227
rs541550769	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877961	CATTTATTGATCTTA[G/T]ACTATTCCAGTTATT	80227
rs541582381	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893083	AATTTAACAGTTTTA[A/T]ATTACTGGACATTCA	80227
rs541582575	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920886	AAATTAAAAAATAAG[A/G]TTGGGTGTAGTGGCT	80227
rs541606326	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912651	CATTTAAGAAAATCA[C/T]AAGTCATGTCACATT	80227
rs541633424	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73881259	GATCTTTTCCCTAAT[A/G]TTTTGCATTTTTCTT	80227
rs541643753	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893777	GAAAGAAAAAACTAA[A/G]CGTGGGCGCGGTGGC	80227
rs541714592	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73927145	AATTTTTGTAAGCAC[A/C]TAATTATGGATGTAA	80227
rs541716209	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73899578	CACCACACACATCTA[A/G]TTTTTGTATTTTTAG	80227
rs541735261	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877754	AGTCGGGCTTGGTGG[C/T]GGGCGCCTATAATCC	80227
rs541832171	snp	A/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73906243	GCTGTATAAATTGAA[A/T]TTCGTTTAGTTTTGT	80227
rs541857172	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73898740	AATCACTTGAGCCTG[G/T]GAGGCAGAGGTTGCA	80227
rs541892395	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73885559	CTAGAAAGCCCTCCC[G/T]GCCTGGTCGTGGTGG	80227
rs541927336	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927991	GTCTCAAACCAACAT[A/G]ATTGGTCAGCCTATA	80227
rs541961040	in-del	-/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886826	GAGGTAGGGCCTAAT[-/G]GGGGGTGTTTGGGTC	80227
rs542190171	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876683	CTTTGAGGACGCATG[A/C]GCGCGCGCGGCCGCT	80227
rs542240821	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906546	GTGAGGCACTGTACC[C/T]GGCCTGGATTTAGTT	80227
rs542241943	snp	A/C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877153	TGCCTGGTCCAGGAT[A/C/T]TCAATAGGGGTTACT	80227
rs542315651	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73896714	TTTCTACACAGACAC[A/G]GCAACCATCCGATTC	80227
rs542425819	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926523	GACCATCCTGGCCAA[C/G]ACGGTGAAACCCTGT	80227
rs542504987	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73918891	TACTATATGTTGAAT[A/G]TAGTCAAGTATTGCT	80227
rs542573479	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73879372	GTTACTTGACCCTGC[A/C]ATATCCAGGAAGCTC	80227
rs542581373	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902757	GCTGGGGTGCAGTGG[C/T]GCGATCTTGGCTCAC	80227
rs542583407	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880672	AGCTTGGATGACTGA[A/G]CAAGACTCTGTCTCG	80227
rs542618471	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73909776	GAATCTACAAAGGAA[A/G]TATATGTCATAGCAC	80227
rs542640786	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912008	CAGTGGTATTTCACA[C/T]AGTAAACCCTCTCCT	80227
rs542753681	snp	A/C	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73909158	GATTTCTCTAGCACA[A/C]TCCACTAAAAATTAA	80227
rs542762740	snp	C/T	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73893112	CAGGTGTTTCCAGTT[C/T]TGTGATTTTGTATTT	80227
rs542795147	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921000	CTACAGGCCATTTTA[C/T]TGATTATTAACATCT	80227
rs542897653	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880232	CATGCTGCGTGGTCT[C/T]CTACCCTGGACCAGA	80227
rs542947593	snp	A/G	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73922690	GGCATCATGGCGGGC[A/G]CCTGTAGTCCCAGCT	80227
rs543003105	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895826	AATTACAAAAGTGAG[A/G]CTGGGCGCGGTGGCT	80227
rs543066163	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887256	GTGGGCCAATTTCAT[G/T]GGTATACTATTTATA	80227
rs543084234	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909044	CACCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT	80227
rs543180507	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907968	GAGGCAATAAGGAAA[C/T]CCAGGAACTCATTGC	80227
rs543258110	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914958	GATCCGCCTGCCTCA[A/G]TCTCCCAAAGTACTG	80227
rs543377706	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73908411	TATGTGTATATATAT[A/G]TGTGTATATATATAT	80227
rs543516189	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915775	TCTAGCTCCTGTGAT[C/T]GTCATCCAGACAACT	80227
rs543629268	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73922205	CATCTTGGTGGCGCC[C/T]GGGTTTCAACCCAGA	80227
rs543818799	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894696	GGGCATGGTGGCACA[C/T]GCCTGTAATCCCAGC	80227
rs543926227	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73900703	AAAGTTGTTTTCTGG[C/T]CGGGCGCGGTGGCTC	80227
rs543941487	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887830	TATTGGCTCACTGCA[A/G]CTTCTGTCTCCTGGG	80227
rs544003093	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906755	ATGTGGTTAATCACA[C/T]TGGATTGGCACTTGT	80227
rs544093891	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875941	CCTCATTTGGTGCCC[C/T]TGGACACATCATTTA	80227
rs544108750	snp	A/G	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73904276	GATTGTAACATATGA[A/G]TTCAATAAGTAATTC	80227
rs544111251	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918080	CTTGTTGAGTAGGAC[A/G]TTGCCAAGTAAAGAA	80227
rs544186794	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924283	AACATGGTGAAACCC[C/T]GTCTCTACAAAAATT	80227
rs544207689	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73889955	GTAAAGAGCATACTG[A/G]TTCAATGATGAGAAT	80227
rs544292029	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904866	TTTGGCTGGGATGCT[C/T]GTATGTGATTCTGCT	80227
rs544319816	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923473	GGGGTGATTTTTGTA[C/T]CTCTGCTTTGTTTAG	80227
rs544321249	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73897370	GCTGCTGGGCGGAGG[C/G]GCTCCTCACTTCTCA	80227
rs544356618	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73896508	GATGACTCTTAAGGA[C/G]CATGCTGCCTTCAAG	80227
rs544410244	snp	A/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73881455	ACCATGCCCAGCTAA[A/T]TTTTGTATTTTTAGT	80227
rs544501358	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909866	TGTCCGATCTTTTGG[C/T]TTCCCTGGGCCACAT	80227
rs544686883	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73880869	CCTGGGCGTGGTGGT[A/G]CATGCCTGTAATCCC	80227
rs544747088	snp	C/G/T	0.000155266	0.00880981	intron-variant	PAAF1	GRCh38.p7	11:73891067	TTAATTATAATACAT[C/G/T]GGAGGAGTTTTACTG	80227
rs544838960	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73917288	CCTCCGAAAGTGCTG[A/G]GATTACAGGCATGAG	80227
rs544942804	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73896943	CTGACCCCCCAGACC[C/T]CCCTCCCCGACGGGG	80227
rs544975013	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924207	CGCTTGTAATCCCAG[C/T]ACCTTGGGAGGCTGA	80227
rs544976369	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904119	TATATACATAAATTG[C/G]TCCCCCAATTGTGTG	80227
rs545088093	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878300	TAGAGGGTTGCTGTC[A/C]ACCTAGATCTTTCTG	80227
rs545149630	snp	A/C	0.00517822	0.0506191	intron-variant	PAAF1	GRCh38.p7	11:73896428	GTCTCTGGTTTTCCT[A/C]GGCAGAGGACCCTGC	80227
rs545190629	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883148	TTATTTTTTAATACA[G/T]GGGGTCTCGCTGTGT	80227
rs545210961	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888317	CAGTTGCCTGATACG[A/G]CCATTACCTACTACA	80227
rs545251915	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73890299	CGTGCTACCTTCAAA[C/T]GCCAATATTCTTACC	80227
rs545253549	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909841	GAGATAAATGCCTAT[A/G]AAGCAGGGGTGTCCG	80227
rs545283695	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73908397	TGTGTGTATATATAT[A/G]TGTGTATATATATGT	80227
rs545366605	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901707	TCCCAAGTAGCTGGG[A/G]CTACGGGTACACGCC	80227
rs545518872	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926641	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	80227
rs545528793	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73920929	CCCAGCACTTTGGGA[A/G]GCCAAGGCGGATAGA	80227
rs545547527	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898665	CTACCGAAAAATACA[A/G]AAATAAGGCACAGTG	80227
rs545554354	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880326	CACACACATATACAT[A/G]TGTATACTTAACATA	80227
rs545686461	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73898052	GTCAGGCGTGGCGGC[A/G]CGCGCCTGCAATTGC	80227
rs545718808	snp	A/C			synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924637	AAGCTGTTTTATTGT[A/C]CAGCAAGACTTAGAC	80227
rs545745545	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73884183	AGAAAACCAAGGCTG[A/C]GGTCATTTTAGTGAC	80227
rs545763321	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73881536	CAAGTGATCCGCCCG[C/T]CTTGGCCTCCCAAAG	80227
rs545795421	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73905940	TTGATTGCTTAATAA[G/T]AGCTGAAAGACCTTC	80227
rs545835928	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877816	GGTTGAACCCAGGAG[G/T]TGGAGGTTGCAGTGA	80227
rs545852636	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876627	AAAAATGCTGGCAGC[C/T]ACGAGGCCTGAGGCG	80227
rs545863388	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73892980	CTTGCTTTTTATTAC[C/T]TAATTATATGTCCAT	80227
rs545886437	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73879677	TCGAGACCAGCCTGG[C/G]CAACAAAGTGAGACC	80227
rs545924797	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884608	CAGTTGGTAAACACA[A/G]TAGGGAATCATGGAG	80227
rs545951287	in-del	-/AAAAAAA			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886692	AAAAAAAAAAAAAAA[-/AAAAAAA]GAAAATGTATTTTAG	80227
rs545954519	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877235	CAAACCCGTATGGTC[A/C]TTCTCTGAAAAGCTA	80227
rs546010509	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875840	GTTAGGCACTTTACA[A/C]AACTCATTTGCCTTG	80227
rs546010542	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882932	TGAGACAGGGTCTTG[A/C]CCTGTTGCCCAGGCT	80227
rs546156998	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890499	CAACCAGTCTATGAA[A/C]ATGTACAGTCAATTT	80227
rs546208452	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912245	CATTCCAAAGTTCAT[A/G]TAAAGCATAGACCTT	80227
rs546250605	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877326	GTTGGAGAAAGACAG[A/G]GATACTGGGAGGCAG	80227
rs546391425	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73925287	TAAGATGAGACCCCC[G/T]TCTCTACAAAAAATA	80227
rs546396840	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925046	TGTAGTTCCAGTTAC[C/T]TGGGAGGCTGAGGCA	80227
rs546413884	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876099	GCCACTGCATTCCAG[C/T]CTGGGTTACAGCGGG	80227
rs546460119	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926050	CCTGTGACTTTTTTT[A/T]AATTACCATCTTAGA	80227
rs546565284	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896977	CTGGCCGGGCGGGGG[G/T]GCTGACCCCCCCACC	80227
rs546595161	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73918550	GGCGCGATCTCGGCT[C/T]ACTGCAAGCTCCACC	80227
rs546618472	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919524	TTGTATATGCAAAGT[C/T]ATAGATGAGGCAAGC	80227
rs546670831	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73881960	GCTCACTGCAACCTC[C/T]GCCTCCCAGATTCAA	80227
rs546690583	snp	C/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909446	AGGAATGTGGTGTCT[C/G]CTTCTCGAGATGGGA	80227
rs546692960	snp	G/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73917534	GAAAATAGCTTCTGT[G/T]GGCATCAGGCTTGGT	80227
rs546705929	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903732	AAAAAAAAAAAAAAT[A/C]TCTTATGAGATTTTG	80227
rs546717750	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882615	CCACGCCTGGCTAAT[A/T]TTTTTGAGACGGAGT	80227
rs546768422	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889851	TCATTTAGTGAAAGG[C/G]CTGCAGGCAGCCAGG	80227
rs546833184	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916837	ATTCCTGGACTCATA[A/T]TAAAATATATGATTC	80227
rs546859436	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73923629	CAACCTCTGCTTCCC[A/G]GGTTCAAGCGATTCT	80227
rs546936441	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73902977	TGCCGGGATTACAGG[C/T]GTGAGCCACTGCGCC	80227
rs546953576	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917786	TGAGGCAGGAGGATC[A/G]CTTGAACCTGGGAAG	80227
rs547047230	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900180	GTTTAGCATGTAGGT[A/G]TTTCATATAAGGGAC	80227
rs547095796	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906957	GAAACAAATACTAGC[C/T]CTGCCTGGATCACCA	80227
rs547228622	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913649	ATCACTATTTCCTTA[A/G]CAGTTAGAATAGTGT	80227
rs547265598	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884803	CCATGACTGCTATTA[A/C]CAAACTGGTGTATTA	80227
rs547304980	snp	C/G	0.127254	0.217792	intron-variant	PAAF1	GRCh38.p7	11:73897125	CTCACTTCCCAGTAG[C/G]GGCGGCCGGGCAGAG	80227
rs547315131	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877554	GTGGAGCTCAGATGT[A/G]TACTCTAAATATAAG	80227
rs547326243	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926799	AACTGGGGCCTGGGG[A/G]GTTGAGAAAGTTGCC	80227
rs547397565	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73884302	CCCAGCAGTTCGAGA[C/T]CAGTCTGAGCAACAT	80227
rs547399849	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900767	GCGGGCGGATCACGA[G/T]GTCAGGAGATGGAGA	80227
rs547544266	snp	A/G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921095	AGCTGAGGTCAGGAG[A/G/T]TTAAGACCAGCCTGG	80227
rs547720668	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73892339	CCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	80227
rs547743091	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875685	AAAAAAAAAAAAGTT[C/T]AGTGATGGGAGAATA	80227
rs547764944	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877919	CGTCTTAATTAGGAA[C/T]ACACAGCAAACTATT	80227
rs547826563	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876076	GCAACACTGTGAGCC[A/G]TGATCACGCCACTGC	80227
rs547859907	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898893	ATAGGGAAAACTTTT[C/T]AGCTGAAGCATTAGA	80227
rs547901851	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920961	CACCTGAGGCCTTGA[C/T]ATTTCTCGCCTCCTC	80227
rs547903700	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912783	TTCTCTCCAGTCTCA[C/T]GTCATACCACCCTCT	80227
rs547974007	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905435	CACCATATTGGCAAG[G/T]CTGGTCTCAAACTCC	80227
rs548045017	snp	A/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73876970	GCACGCTTCTCGGGG[A/T]CTCACTTCCGGGAAG	80227
rs548077004	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73892276	TGCAGTGAGCCATGA[C/T]CATGCCACTGCACTC	80227
rs548150853	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898107	AGAATCAGGCAGGGA[A/G]GTTGCAGTGAGCTGA	80227
rs548166281	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73883426	GTTTACTTTCTAGCT[C/T]TGTGGATTTGCCTAC	80227
rs548203989	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73926389	AGGCGTGAGCCACCG[C/T]GCCCAGCCATCTATT	80227
rs548212773	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891635	CAAAAATTAGCTGAG[C/T]GTGGTGGCACTTACC	80227
rs548216620	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906793	GCTGAGTTGCTGTAG[A/G]GTTTTTGTCAAGGTT	80227
rs548224841	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897321	GACGAGGTGGCTGCC[A/G]GGCGGAGACGCTCCT	80227
rs548858410	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917750	GGTGGCACGTACCTA[C/T]AATCCCAGGTACTGG	80227
rs548860215	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73925212	CTGTAACCCCAGCAC[C/T]TTTGGAGGCTGAAGC	80227
rs549015614	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73886274	TTCATCCTGGAAGAA[-/T]TACATTTCACAGCCA	80227
rs549112213	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879634	ACTTTGGGAAGCTGA[A/G]GCAGGAGGATCACTT	80227
rs549248143	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893322	AAACATACCGTTAGG[C/T]TGAAAGTTTATCAAG	80227
rs549283839	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900727	GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG	80227
rs549323549	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879059	GTTGATGCATCTTAA[G/T]TAGTCACTTACCCTG	80227
rs549377568	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921847	GGTTTGGGATACATT[A/G]CATTAAGTGGAAAAC	80227
rs549399597	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895188	GATGACTTGGATGTT[A/C]AGTATGAGAGAAAAG	80227
rs549421019	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73883419	ACCACTAGTTTACTT[C/T]CTAGCTCTGTGGATT	80227
rs549441929	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73914307	GTTTTCTTTGTAATA[A/C]GTGAATCGCTAACAA	80227
rs549472973	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73900843	AAAAATTAGCCGGGC[A/G]TAGTGGCGGGCGCCT	80227
rs549526021	snp	C/T	0.00993419	0.0697739	intron-variant	PAAF1	GRCh38.p7	11:73911333	GACTCTAGGCATGCA[C/T]CACTACACCTAGCTA	80227
rs549635442	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885261	CTCCTGCTTCAGCCT[C/T]CTGAGTATCATAGCT	80227
rs549659083	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73878933	TAATAGTCTGCAAAC[A/G]TGCTTGACCAGTCTG	80227
rs549688369	snp	C/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875039	ATATGGGTAGGTTTT[C/G]ACACATGGGAAGGAT	80227
rs549752011	snp	G/T	0.0209421	0.100162	intron-variant	PAAF1	GRCh38.p7	11:73896922	GCGGCTGGCCGGACG[G/T]GGGGGCTGACCCCCC	80227
rs549768198	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878208	ATAACATGAAGTGCC[A/G]CTAGCTACCTATGAG	80227
rs549831885	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73913708	AAAAAAAGAAAAAAA[A/G]AAAGAAAAAAAGAAT	80227
rs549839445	snp	A/G	0.0178098	0.0926698	intron-variant	PAAF1	GRCh38.p7	11:73908259	TGTGTATATATATGT[A/G]TATATGTGTATATAT	80227
rs549955625	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902585	ATACCTTTGGATCAC[C/T]GCAATTATTGTTCCC	80227
rs549966541	snp	A/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888919	GGATGAATCTATAAA[A/T]TACTACAGAAGTTAG	80227
rs550003281	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73895524	ATGTTAGAGTTGATG[C/G]ATATATCCCTATAGT	80227
rs550105273	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884920	GCTGGAGTGCAGTGG[C/T]GGGATCTCGGCTCAC	80227
rs550140843	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892401	GATATATACTTAGTG[A/G]TGAAAATTTAGGACA	80227
rs550164042	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875448	CCTAGACAAGGAAAC[A/G]GGGCAGTTTACTACA	80227
rs550193889	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927686	AAGGACCTCAGTACT[A/G]AAGCCTGTTCTCTGG	80227
rs550195292	in-del	-/TGTC			intron-variant	PAAF1	GRCh38.p7	11:73890845	TTGTATCATATTGTT[-/TGTC]TGTCTTCTGTGGAGC	80227
rs550229985	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73901605	GATCAAGTTTTAAGA[-/T]TTTTTTTTTTTTTTT	80227
rs550629447	snp	G/T	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73881261	TCTTTTCCCTAATAT[G/T]TTGCATTTTTCTTGC	80227
rs550748404	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909344	CTCCATCTTCTCTGC[C/T]CTTGTAGTTCCTTTA	80227
rs550757104	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922445	AAGGTAGTGGGCACC[C/T]CTAACTCTGGAGATG	80227
rs550786225	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888927	CTATAAAATACTACA[C/G]AAGTTAGTTTTGGTT	80227
rs550852819	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887553	TTATCTGTGTATCTC[C/T]ACTTCATTTGTATGA	80227
rs550905063	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902857	ATGCGCCACCATGCC[C/T]GGCTAATTTTTTTTT	80227
rs550940192	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73908839	TCTGTTGAAGGCTGG[A/G]GTGCAGTGGCGTGAT	80227
rs550951192	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73904457	TATTTTAGTTAACTA[A/G]TTGGCTTTATTTTTA	80227
rs550970017	snp	G/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73881225	GAGCAAAACATCAAC[G/T]GGGGTTTATATTTTT	80227
rs551043897	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902431	GTCTAGAGGAACAGT[C/G]CAAGCTTCACCTCCG	80227
rs551071077	in-del	-/A	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73902706	TATTTATTTATTATT[-/A]TTTTTTTTGAGATGG	80227
rs551073111	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916216	GCAAGTGTTTCTCAG[A/G]AAGTTGTCATGAAAA	80227
rs551122079	snp	C/T	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73879790	CAATAGGAGGATCTC[C/T]TGAGCCCGGGAGGTT	80227
rs551179235	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73885207	GCAATGGCGTGGTCT[A/C]GGCTCACTGCAACCT	80227
rs551180276	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896671	TTCTTAGTACGGAAC[A/G]AAATGAAAAGTCTCC	80227
rs551200651	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73906346	CAACCTCTGCCTCTC[A/G]GGTTCAAGTGATTCT	80227
rs551242504	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73882364	AGTTTTCTTTATGAA[C/T]TGGAGTTAATGATGT	80227
rs551278405	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901753	TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC	80227
rs551463505	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73922812	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA	80227
rs551564699	in-del	-/C	0.0894459	0.191631	intron-variant	PAAF1	GRCh38.p7	11:73896982	GGGCGGGGGGGCTGA[-/C]CCCCCCCACCTCCCT	80227
rs551632623	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902825	CCGCAGCCTCCCCAG[C/T]AACTGGGATTACAGG	80227
rs551729676	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915405	TGAGTCCAGGAGTTC[C/G]AGACTGGCCTGGGCA	80227
rs551817297	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926255	GGGATTACAGGCATG[C/T]GCCACCACACCCGGC	80227
rs551867226	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922321	AGTAAGATTATAACT[C/G]TGTTTTCAGAGGACA	80227
rs551884659	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876707	GGCCGCTGATCGCAG[C/T]CCCGTTGTGCCCGCA	80227
rs551927930	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880543	ATACAAAAAATTAGC[C/T]GGATGTGGTGGTGGG	80227
rs551945841	snp	C/T	0.00993419	0.0697739	intron-variant	PAAF1	GRCh38.p7	11:73908112	CTAGGAGCAATGGGA[C/T]TACTCTTTCTTGGCC	80227
rs551953285	snp	A/T	0.0287284	0.116357	intron-variant	PAAF1	GRCh38.p7	11:73925462	CAGAGTGAGACCCTG[A/T]CTCAAAAAAAAAAAA	80227
rs552003600	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884510	AAATATTAAAAAAAT[A/G]CATATATATACATCC	80227
rs552019392	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886577	TGTTCGGAGGCTGAA[A/G]CAGGAGAATGGTGTG	80227
rs552135442	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73920303	TTTTGGGAGGCTGAG[A/G]CGGGAGGATCACTTG	80227
rs552183829	snp	G/T	0.0314385	0.121371	intron-variant	PAAF1	GRCh38.p7	11:73897554	AGACGATGGGCGGCC[G/T]GGCAGAGACGCTCCT	80227
rs552198639	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912748	TTACAACAAGCTCTT[A/G]TACTTTCTGACCCCT	80227
rs552205065	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878290	CGTCAAATGATAGAG[A/G]GTTGCTGTCAACCTA	80227
rs552370431	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882695	GCAAGCTCCGCCTTC[C/T]AGGTTCATGCCATTC	80227
rs552400625	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910266	AGGTTTTCAGAGGGA[C/T]GGAGTGTTCCCGGTT	80227
rs552407546	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876257	GGGCCAGGAGCAAAT[A/C]ATTTAGAGAAAGAAC	80227
rs552448149	snp	A/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73881771	GAGTGCAGTGGTGCA[A/T]TCTTGGCTCACTGCA	80227
rs552480490	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917598	GGCTCTGGGCTGGGC[A/G]TGGTGGCTCACGCCT	80227
rs552485018	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875217	CAGAAAGCAGCATAC[A/G]GAAGGAACTTAAGGT	80227
rs552514185	snp	A/G	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73897051	CTTCCCAGTAGGGGC[A/G]GCCGGGCAGAGGCGC	80227
rs552644349	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73910968	GCACTCCAGCCCAGG[C/T]GACAGTGTGAGACTC	80227
rs552796200	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923792	ATGATTCATTTGTTT[C/G]ATTTGTCCATGCTCT	80227
rs552882521	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73924192	GGGTATGGTGGCTCA[C/T]GCTTGTAATCCCAGC	80227
rs552898015	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886965	GCATCTCCCTTCTCT[C/G]TCTTACTTCCTCTCT	80227
rs552927886	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73924473	AAAAAGTTGGCCCAC[A/G]TAATAAGATCTATTT	80227
rs552983623	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924825	TTGTATAAGCAGTGT[A/G]GTAGGATGGCAAGAA	80227
rs553056657	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917235	CATGTTGGTCAGGCT[A/G]ATCTCGAATTCCTGA	80227
rs553088917	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73921647	AGATGGTGGCTGCCC[A/G]TGCTCCTTTCACTGT	80227
rs553118123	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917839	TCGTGCCACTGGACT[C/G]CAGCCTGGGCAACAG	80227
rs553122038	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909795	ATGTCATAGCACTGC[A/G]TTTCAGTAAGTACAA	80227
rs553131582	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73908363	TGTATATATGTGTGT[A/G]TATATATATGTATAT	80227
rs553133221	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73916323	CTTCAGAGTATATTA[C/T]ATAACCTGCTCAAGT	80227
rs553177289	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881300	ACTATTAAAGCAGTA[C/T]TTTTTAAACAGAATC	80227
rs553188675	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73908874	GGTCACTGCAACCTA[C/T]GCCTCCCAGGTTCGA	80227
rs553289786	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880727	AAAAAAGCCAGGCAC[A/G]GCAGCTCACGCCTGT	80227
rs553293874	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888994	AATTTCCATTTTGCA[A/G]ATAAGCAAACCAACT	80227
rs553342240	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922516	GAGGGAGTTCTGTAC[A/T]GGTTTAGAAGTTGGA	80227
rs553359887	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896752	TTTCCCCACCTTTCC[C/T]CCCTTTCTATTCTAC	80227
rs553411572	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893951	GTAGTCCCAGCTAGT[C/T]GCCTGGCTTAAAAAT	80227
rs553474622	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73892071	CTCATGCCCGTAATC[C/G]TAGCACTTTGAGAGG	80227
rs553474672	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916973	TCAGTAATTTTCTCT[C/T]ACATTAGACCCTGGC	80227
rs553529804	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906037	TATTATGGAGTTGAA[A/G]TAGAAATGTAGATTT	80227
rs553570259	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902052	TATTTTTTAGTAGAG[A/G]TGGGGTTTCGCTGTG	80227
rs553667275	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912160	TACTAGAGGGCCCCA[C/T]TATTAAGTTCTGGGC	80227
rs553694669	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73892850	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	80227
rs553722696	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883618	ACCTCCCAGGTTCAA[C/G]TGATTTTTGTGCCTC	80227
rs553726445	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73898627	TTTGAGACTAACTTG[A/G]GCAACATGGTGAAAC	80227
rs553737962	in-del	-/AAAAAAAAAAAAAAA	0.471768	0.115407	intron-variant	PAAF1	GRCh38.p7	11:73900982	GCGAGACTCCGTCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	80227
rs553789609	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73890740	TCTCTTTATGTCCTC[G/T]TCGCACTGATCCTGT	80227
rs553832195	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884524	TACATATATATACAT[C/T]CACAAATGTGGAGAA	80227
rs553833151	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882817	ACCGTGTTAAGCAGG[A/G]TGGTCTCGAACTCCT	80227
rs553869533	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919181	GTGTTTATCACTCTA[C/T]GTTGTGATTGTCTGT	80227
rs553914193	snp	A/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73890356	AAGTCATGTCTCCTG[A/T]ATCTAACATCTGGTT	80227
rs554001041	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73925960	AATTTGCACACTTAC[A/G]TCTTTATGTATTAAT	80227
rs554125149	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926425	TTTAAAAATTCTTGC[A/G]TAGTGTTCCGGCCGG	80227
rs554147808	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73876987	TCACTTCCGGGAAGG[G/T]GCGGAAGAGGTGGGC	80227
rs554173362	snp	A/G	0.0130921	0.0798413	intron-variant	PAAF1	GRCh38.p7	11:73897277	GGCGGCTGGCCGTGT[A/G]GGGGGCTGACCCCCC	80227
rs554263747	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73896110	TGAGACCCTGTCTTT[-/A]AAAAAAACACAAAAA	80227
rs554309446	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73897816	ATCTCGGCACTTTGG[A/G]AGGCCAAGGCAGGCT	80227
rs554316420	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899084	GGAAGTTTATAACAT[A/G]TTTCAAGGGAATAAG	80227
rs554445090	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911429	CTCAAGTGATTCTCC[C/G]ATCTTAGCCTCCCAA	80227
rs554569252	snp	G/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73898463	TCAAGTAATCTTCCT[G/T]CCTTGGCCTCCCAGA	80227
rs554569676	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73923650	AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA	80227
rs554618945	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882177	TGAGCCACTGTGCCC[C/T]GCAATTTTTTGTATT	80227
rs554650766	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905687	AGAGGGTGATAATTT[C/T]CCACTCTGCTTTTAT	80227
rs554785475	snp	C/T	0.0107246	0.0724382	intron-variant	PAAF1	GRCh38.p7	11:73926138	TGAGATGGAGTTTCG[C/T]TCTTGTTGCCCAGGC	80227
rs554789459	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912071	TACCACATAACACTG[A/G]TTTTCTTCCTATTTC	80227
rs554791326	snp	C/T	0.0283406	0.115616	intron-variant	PAAF1	GRCh38.p7	11:73897188	CGTGCGGGGGGCTGA[C/T]CCCCCCACCTCCCTC	80227
rs554893310	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886979	TCTCTTACTTCCTCT[C/G]TCACCATGTGATCTC	80227
rs555033621	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73886166	CAGTATTCTACTTAG[A/G]CAAATTTTACAGGTT	80227
rs555080325	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879868	ACAGAGTGAGACCCC[A/C]TCATTAAAAAAAAAA	80227
rs555129757	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903911	AAACATGGTAAAACC[C/G]TGTCTCTACAAAAAA	80227
rs555167833	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73894421	GGGGTGGGCAGATCA[A/G]TTGAGGCCAGGAATT	80227
rs555330184	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922054	TGGCCTTGAACTAAT[A/C]GATGGCTTCATCCAC	80227
rs555343944	in-del	-/T	0.0543581	0.155641	intron-variant	PAAF1	GRCh38.p7	11:73918485	TCTTTTTTTTTTTTA[-/T]TTTTTTTTTGAGATG	80227
rs555403206	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73883392	GTCACTTTCCACCCC[C/T]CAATCCTAGCAACCA	80227
rs555465293	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73881115	GTCCACTTATTATTA[C/T]AAGGACCTTGGCTAT	80227
rs555555939	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878270	TTGCCCAAGATCATG[C/T]ATCTCGTCAAATGAT	80227
rs555657333	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73891380	GTACTCTAGTCCACA[C/T]AGAATATGTGTTCAA	80227
rs555769853	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907129	ATAATCAACTCTATT[G/T]TTTTATGCTGTGTAT	80227
rs555812980	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73926532	GGCCAACACGGTGAA[A/G]CCCTGTCTCTACTAA	80227
rs555848513	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73893694	GTGAGCCAAGATTGC[A/G]CCATTGCACTCCAGC	80227
rs555852899	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920861	TGTCTCAAAAAAAAA[A/C]AAAAATTAAAAATTA	80227
rs555880407	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884471	CTGCACTCCAGCCTG[A/G]GTGACAGAGCGAGAC	80227
rs555916128	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73921374	GGAGAAGAGCTGACT[C/T]ATGGTTCTACTTTTT	80227
rs555919095	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73886120	TTTATGTGTAGGATA[A/G]TATCTTACTTAGCCC	80227
rs555919571	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73927114	GATTGGGATGCATCC[A/G]TCACTATGGGCCAAC	80227
rs555926070	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899528	GCGATTCTTGTGCCT[C/T]AGCCTCCCAAGTAGC	80227
rs555966288	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877663	AACTGAGATTGGTGG[A/T]TCAGTTGAGGTCAGA	80227
rs555980011	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73890100	ACCAGAGACTTTGAA[C/G]TACTACTGCAGAAGA	80227
rs555990512	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73910798	GCTCGAAACCAGTCT[A/G]GCCAACATAGTGAAA	80227
rs556062745	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906498	TCGAGTGATCTGCCC[A/G]CCTCAGACTCCCAAA	80227
rs556066272	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907003	TCTCTACTCCATACA[A/G]CTCTGTGTTTTTACA	80227
rs556095824	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885470	TCTTGATATGCTCCT[A/C]CTTGACTTGGAGTTT	80227
rs556105569	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877570	TACTCTAAATATAAG[C/T]GATGGTTCCTGCTCT	80227
rs556154739	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73891657	GCACTTACCTGTAGT[A/C]CTAGCTACTCAGGAG	80227
rs556214366	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914338	AATCAGTAATCAACC[A/G]TCAGTATTGGTGCTG	80227
rs556219943	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877074	AAGCCCTCAGGTGAA[A/T]CCAGGCCCAGAACAG	80227
rs556234921	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878643	GAATGATCTATACTC[A/G]ATGAGAGGTTGGACT	80227
rs556377943	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904341	CCCAGGCCATTTAAG[G/T]AAGCTTGTGAAATTT	80227
rs556380338	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73913004	GCCTCAGCCTCCCGA[A/G]TAACTGGGATTACAG	80227
rs556474529	in-del	-/CT	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73891753	GCACTGCAGCCTGGA[-/CT]CTGTCTCCAAAAAAT	80227
rs556631472	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73889583	GATTTGCAAGACTGC[A/G]AAGTAGGAGAAAAGT	80227
rs556633892	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886741	ATTCCCTTTCAAATT[A/G]GAGTTTAGTGCTATA	80227
rs556643525	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73923413	AAATAGGCACAAAAA[A/T]ATAGATCAAAATGTT	80227
rs556851324	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888047	GCTACCATGCCCAAG[C/T]GAAATTGATTTTAAT	80227
rs556902119	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898405	ATTTTTTGTAGAGAT[G/T]GAGTCTCATTATATT	80227
rs556906645	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73883981	GGCAGGATAGATGGC[A/G]TGAGAACCAGCTGCT	80227
rs556991706	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917082	CTGGAGTGCAGTGGT[G/T]CTATCTCGGCTTACT	80227
rs557000641	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909418	CCTGGATACAGCCAT[C/T]GTTGATCGGGGGAGG	80227
rs557050649	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923208	AAGGTACTACCTCGT[A/C]TATGCTGCTGCTTGA	80227
rs557095680	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912360	ACCCCAAACTGTTTT[C/T]TTCCATCTCAGAAGA	80227
rs557109813	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916483	TTCCTTTTTTGGTGC[C/G]TGTTTATTCTTGGAA	80227
rs557149764	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73907685	GGGAGTGCTGCTGCC[A/G]GCTTCCATGGGAGCG	80227
rs557169928	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73927210	TGGGACTAGTGTGTG[A/T]CAATCATAAGCCTCC	80227
rs557198471	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73908319	TATGTATATATATGT[A/G]TATATATGTATATAT	80227
rs557231773	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887239	GCACCTGTTTTTCTT[A/T]CGTGGGCCAATTTCA	80227
rs557265097	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921983	CGTAGACAGAGATAC[A/G]TATATCAAGGTCCTG	80227
rs557304099	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896192	TTTATTCTGAAAGAT[C/G]TATATCTGTATATTT	80227
rs557387002	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907913	CCTGTTAGCAGTTTT[A/G]TGTTGGAGGCTTCTG	80227
rs557433815	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73924382	ACCTGGGAGGTGGAG[A/G]TTGCAGTTTGCTGAG	80227
rs557498414	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886310	ATCAGGTTGAGATCA[C/T]TCTAAAAGCCCTCTC	80227
rs557698637	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887196	CCTAATCTAATTCTC[C/T]TTTTACTTCACCTGA	80227
rs557758423	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887238	GGCACCTGTTTTTCT[C/T]TCGTGGGCCAATTTC	80227
rs557900455	in-del	-/CT	0.0126979	0.078662	intron-variant	PAAF1	GRCh38.p7	11:73896252	GTGGAAATATCTGAA[-/CT]CTTTTTTTTTTTTTT	80227
rs557958962	snp	C/T	0.000399281	0.0141238	intron-variant, stop-gained, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889240	CCTGCTGAGTGGGTT[C/T]AGACAGTAAGTGCTT	80227
rs557992511	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914772	CAGTGGCGCAATCTC[A/G]GTTCAGCTCACTGCA	80227
rs558074306	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73909741	ATTTACTCTGTACCT[A/G]CTATGTTTCTATTAC	80227
rs558088511	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901932	GCAGTGATGCCAGCT[C/T]GGCTCACTGCAACCT	80227
rs558225499	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901410	TATTCCTATTTTACA[A/G]GTTTGAATATTTTAA	80227
rs558235141	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73900612	TTGCTATCTTGAACT[A/G]TCTTACACAGTTGGT	80227
rs558293529	snp	A/T			utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927629	GGGCAAGGATATAGA[A/T]GCTTTTAGTTTGTTC	80227
rs558301812	in-del	-/AA	0.0726307	0.176182	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876127	GGGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAAGA	80227
rs558305216	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907161	CCTGAGGCTAGGGAC[C/T]ATAGCAAATATTCAG	80227
rs558324912	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910606	CTGTTCCATAGGACA[A/G]TGTTTTTTCTACTGT	80227
rs558355685	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878415	AATAATAAAAGGAAT[C/T]TTGTTTGGTTATTGT	80227
rs558400371	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73924228	GGGAGGCTGAGGCAG[A/G]TGGATCACCTGAGGT	80227
rs558471580	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73917889	AAAAAAAAAAAAAAG[A/G]TACAGACTCTGCCTT	80227
rs558473808	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877763	TGGTGGTGGGCGCCT[A/G]TAATCCCAGCTACTC	80227
rs558568168	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73904839	CATCTAATGTTATTC[A/G]TATTTCCAGACTTTG	80227
rs558648323	snp	A/G	0.00362756	0.0424337	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889093	GATTCCAAGTTTAGC[A/G]CTACCATGCAAGCCT	80227
rs558705805	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904245	AAGTGGAAAGGTAGA[C/T]TAAAAGTAGTTTTGT	80227
rs558709663	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902614	CCTTTACAGAATCCT[A/G]AGTCTCCCAACATTC	80227
rs558772594	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902999	CACTGCGCCCGGCCT[A/C]GAATGTTAAATCAAT	80227
rs558790641	snp	A/G	0.00835141	0.0640778	intron-variant	PAAF1	GRCh38.p7	11:73896839	GACGGGGTGGTGGCC[A/G]GGCAGAGGGGCTCCT	80227
rs558873420	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882018	TAGCTGGGATTACAA[G/T]CATGTGCCACCATGC	80227
rs558941343	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889954	TGTAAAGAGCATACT[A/G]ATTCAATGATGAGAA	80227
rs558946842	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916409	GTGAATGTGTAATTT[A/C]CCATTTGAGAATAAT	80227
rs558966881	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888709	ACATGTTATTATATA[C/T]TTTATATTTGTTTTT	80227
rs559150747	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896438	TTCCTAGGCAGAGGA[A/C]CCTGCGGCCTTCCGC	80227
rs559218216	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877564	GATGTATACTCTAAA[C/T]ATAAGTGATGGTTCC	80227
rs559228724	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73899024	AACACAAGTCCTTTT[A/G]TTGGGAAACACAGGC	80227
rs559271722	in-del	-/T	0.257176	0.249897	intron-variant	PAAF1	GRCh38.p7	11:73901871	CCACTGCGCCTTGCC[-/T]TTTTTTTTTTTTTTT	80227
rs559341373	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73896931	CGGACGGGGGGGCTG[A/G]CCCCCCAGACCTCCC	80227
rs559444457	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909191	CCAGTACTTGTTTTT[C/T]CATGCCTGTCTTTCA	80227
rs559535742	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880290	AACACACACACAAAT[A/G]CACAAATATATATAT	80227
rs559577099	snp	A/T	5.1705e-05	0.00508427	intron-variant	PAAF1	GRCh38.p7	11:73916701	GCAGGTCTTCTGCAG[A/T]GTGGAAATTTTTATT	80227
rs559626816	snp	C/T	0.00358779	0.0422022	intron-variant	PAAF1	GRCh38.p7	11:73923382	ATTCGTTTATGCACA[C/T]GCTGTCAACCATGTA	80227
rs559671366	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901613	TTTTAAGATTTTTTT[G/T]TTTTTTTAAGATGGA	80227
rs559706586	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922300	CTGATGTCTAAAGGC[A/G]AAGGGAGTAAGATTA	80227
rs559712853	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915899	AGGAACATTACCATT[G/T]TTGCTAATATCGCCT	80227
rs559749036	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887310	AAGAGAAAAATAATA[A/C]ATTTTTCTTATTTTT	80227
rs559756881	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917250	GATCTCGAATTCCTG[A/G]CCTCGTGATCTGCCC	80227
rs559798984	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895832	AAAAGTGAGGCTGGG[C/T]GCGGTGGCTCACGCC	80227
rs559814129	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907981	AATCCAGGAACTCAT[G/T]GCTGTGTTGTTTTTT	80227
rs559815078	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902818	TCTCCTGCCGCAGCC[C/T]CCCCAGTAACTGGGA	80227
rs559818580	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874753	AGCAATTTGGGAGCC[C/T]GAGGCAGATGGATCA	80227
rs559823202	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896577	CCATTCAACCCTGAG[C/T]GGATACAGCACATGT	80227
rs559889605	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886542	TAGCCGACATGGTGG[C/T]GGGTGCCTGTAGTCC	80227
rs559897465	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918728	ACCTTAAAAACTCAG[G/T]ATTTGGGTGGTGACT	80227
rs559903759	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875717	AGTGTGAGAATAAGA[C/G]AATATTAAACTGGCG	80227
rs559951320	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73907469	GGACACAGTTGCACC[A/G]CCTGACTTGCATCAC	80227
rs559974199	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73904495	TCTCATAATGGTAGT[A/G]GAAATGCTTACATTT	80227
rs560013598	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900754	TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	80227
rs560030458	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73894784	AGCCGAGGTTGCGCC[A/G]CTGCACTCCAGCCTG	80227
rs560032155	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73905099	TAGCAATGGCACTCT[A/G]GTCTGGGCAATATAG	80227
rs560103944	snp	C/G	0.0115144	0.0749975	intron-variant	PAAF1	GRCh38.p7	11:73926631	GGAGAATGGCGTGAA[C/G]CCGGGAGGCGGAGCT	80227
rs560111105	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910904	CTAAGGCAGGAGAAT[C/T]GTGTGAACCTGGGAG	80227
rs560208512	snp	C/G/T	0.0091479	0.0670627	intron-variant	PAAF1	GRCh38.p7	11:73897553	CAGACGATGGGCGGC[C/G/T]GGGCAGAGACGCTCC	80227
rs560338518	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891406	TTCAAATCTACTCAC[A/T]GGTCATCTTAGAGAT	80227
rs560349401	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890375	TAACATCTGGTTCTA[A/G]GTATAGTTTCCTAAT	80227
rs560359974	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916081	ATTTTTTTTTTCAGA[C/T]TCATGGGGAGAATTG	80227
rs560410597	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73911837	TGAGGTTTCACCATG[C/T]TGGCCAGGCTGGTCA	80227
rs560492111	in-del	-/A	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878511	AATTAAATAACCTTG[-/A]ATTTTTCAAAGTGAG	80227
rs560531461	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924446	AACGAAACTCTGTCT[C/G]AAAAAACAAAAAAAA	80227
rs560569070	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875181	CCAAACTGTCTTGCC[C/T]GTCTGCATCAGAACA	80227
rs560613103	in-del	-/C	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73916909	AAGCTTAAATATAAA[-/C]TAACATTTCATTTAA	80227
rs560669860	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918349	CATCATTTCAGTTAC[C/T]TAATTTTTTTTTTTT	80227
rs560682879	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73882596	GGATTTCAGACATGC[A/G]CCACCACGCCTGGCT	80227
rs560771762	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876039	GAGGCTGAGGCGGGA[A/G]GATGGTTTGCGCCCA	80227
rs560887092	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73921136	GAAACGCCATCTCTA[A/C]TAAAAATACCAATAT	80227
rs560939435	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917394	ACCTTTCTAAACAGG[C/T]TTTTCTTTGGCCTTA	80227
rs560966920	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890615	TCTGGTCATTGTAAA[C/T]GTCAGTAGTCTAACA	80227
rs561013813	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923574	AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	80227
rs561041692	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73896971	GGGCGGCTGGCCGGG[C/T]GGGGGGGCTGACCCC	80227
rs561050971	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73896024	TCAGGCAGGAGGATC[A/G]CTTGTTCCTGAGAGG	80227
rs561075960	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924291	GAAACCCCGTCTCTA[C/T]AAAAATTAGCCAGGC	80227
rs561103229	snp	C/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73897424	GGGCTCCTCACTTCT[C/G]AGACGGGGCGGTTGC	80227
rs561128628	in-del	-/A	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73908787	ACTTAATTTTTATTT[-/A]TTTATTTATTTATTT	80227
rs561198936	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874996	CATCTCCAAAACAAA[C/G]AAACAAACAAAGTGA	80227
rs561214756	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919163	ATATTGTACCTATCA[A/G]TAGTGTTTATCACTC	80227
rs561241998	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73892151	AACATGGTGAAACTC[C/T]GTCTCTACAGAAAAA	80227
rs561249832	snp	G/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73910821	TAGTGAAACCCCATC[G/T]CTACTAAAAATACAA	80227
rs561262144	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876891	ACGGAAGGGGCGGGG[-/A]AATGTGAAAAAGTCA	80227
rs561286408	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875140	GCTTTGTAAACTATA[C/T]AAAAATGTGAGGTGT	80227
rs561302363	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73912286	TTCAGACTCTATTTC[A/G]ATGTCTAATAAATAA	80227
rs561335715	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73914116	ATTTGGATTTACTGA[G/T]GTATCTTTTACATAT	80227
rs561347960	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73880893	TAATCCCAGCTACTC[G/T]GAAGGCTGAGGCAGG	80227
rs561446842	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881462	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGAGACA	80227
rs561471948	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921558	ACATGGTCTTCTCTC[G/T]TCTGTATAAAACTTT	80227
rs561473830	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913445	ATAAAAAATATTTTA[A/G]AAAATAAATAAAGTT	80227
rs561510248	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884756	ACCCTAGACTTTGAG[G/T]TTCTCTGGGATTTAT	80227
rs561571816	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73885599	GTAATCCCAGCACTT[C/T]GGGAGGTTGAGGTGG	80227
rs561594454	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73928011	GTCAGCCTATATGTA[A/G]GTGAGGAAACTGAAT	80227
rs561614647	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878717	CTTCTTTCTTCCCTT[C/G]TAACTATGGGATCCT	80227
rs561786318	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73892281	TGAGCCATGATCATG[A/C]CACTGCACTCCAGCC	80227
rs561966896	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877992	TCTCTAGGCTTCAGG[A/G]TGAATATAGCAGTGC	80227
rs561978747	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899616	GGGCTTTCGCCATGT[C/T]GGCCAGGCTGGTTTC	80227
rs561995831	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73905305	CTCAGCTCAGTGCAA[C/T]CTCCGCCTCCTGGGT	80227
rs562120037	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73912533	CCTCCCCCTCTCTCC[C/T]TTCCTCCTGTCAACA	80227
rs562260307	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920221	AAAATATAATATTTT[G/T]TATATATTTTTTTAA	80227
rs562260358	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73911738	TCAAGTGTTCGAGTG[A/G]TTCTTGTGCCTCAGC	80227
rs562273508	snp	A/C/G	4.954e-05	0.00497674	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927319	AGATCTACACATGCT[A/C/G]TCGAGACGGTCTTGT	80227
rs562393602	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919360	AGTTTGATAAGGACT[A/G]CATCAGAAGACTGCA	80227
rs562405077	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906139	ATAGATCTGTTTTTG[A/C]AAGGAAGACTGAAAA	80227
rs562405113	snp	C/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73898075	GCAATTGCAGGCACT[C/G]GGCAAGCTGAGGCAG	80227
rs562453031	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884609	AGTTGGTAAACACAA[C/T]AGGGAATCATGGAGT	80227
rs562467039	in-del	-/A	0.190737	0.246058	intron-variant	PAAF1	GRCh38.p7	11:73894634	TTAAAGTATAATAAT[-/A]AAAAAAAAATCTACT	80227
rs562585318	snp	A/C	0	0	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877336	GACAGGGATACTGGG[A/C]GGCAGGAAGGCTTTT	80227
rs562608422	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888017	CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG	80227
rs562662733	snp	G/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73891545	CTTTGGGAGGCAGAG[G/T]CAGGAGGATCACTTG	80227
rs562697382	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875861	ATTTGCCTTGGAGGC[A/G]GTATAACTTAAGCAA	80227
rs562950120	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918484	TTTCTTTTTTTTTTT[A/T]ATTTTTTTTTGAGAT	80227
rs563035873	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911603	GAAATGGCTGTTGTT[A/G]AAGTCACCAGTGACC	80227
rs563083080	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926054	TGACTTTTTTTTAAT[A/T]ACCATCTTAGAGCTG	80227
rs563104797	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73900937	CAGTGAGCCGAGATC[C/G]CGCCACTGCACTCCA	80227
rs563212477	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73882485	GAGTTTCGCTCTTGT[C/T]GCCCAGGCTGGAGTG	80227
rs563221556	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925081	AATCGCTTGAACCTG[C/G]GAGGTGGAGGCTGCA	80227
rs563252992	snp	A/G	0.0103295	0.0711199	intron-variant	PAAF1	GRCh38.p7	11:73908417	TATATATATGTGTGT[A/G]TATATATATATGGGT	80227
rs563347466	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73908229	AATAAATATATATAT[A/G]TGTGTGTATATATAT	80227
rs563439291	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926390	GGCGTGAGCCACCGC[A/G]CCCAGCCATCTATTT	80227
rs563498805	in-del	-/GGAGAA	0.104504	0.2033	intron-variant	PAAF1	GRCh38.p7	11:73898245	GAGGGAGAGGGAGAG[-/GGAGAA]GGAGAGGGAGAGGGA	80227
rs563509978	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73906364	TTCAAGTGATTCTTG[G/T]GCCTCAGCCTCCCAA	80227
rs563580542	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886413	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	80227
rs563603746	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922208	CTTGGTGGCGCCCGG[A/G]TTTCAACCCAGAGGA	80227
rs563660072	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894718	AATCCCAGCTACTCC[A/G]GAGGCTAAGGCACAA	80227
rs563727165	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907215	AAAACTATAAAATCG[A/G]TAGGCATTTTGGACA	80227
rs563728418	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73878948	ATGCTTGACCAGTCT[A/G]TACTGTATGGCCAAC	80227
rs563733398	snp	C/T	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73909855	TAAAGCAGGGGTGTC[C/T]GATCTTTTGGCTTCC	80227
rs563764157	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874842	AATACAAAAATTAGG[C/T]GGGCGTGATGGCAGG	80227
rs563860902	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913998	AAGACTGTGGGGTGC[C/T]ATGTTTGTGCTTGTG	80227
rs563870239	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899911	CCTCCAACCTTTACA[A/G]AGGATTTTAAACAGA	80227
rs563983935	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879425	TTGAACAACAGTCTT[A/G]TATCATTCACAGGAT	80227
rs563994526	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902326	CAGAGCCTTCCTTAC[A/G]TTACTGAAGAACTCA	80227
rs563999420	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922160	AATGAGTTCAGTGTC[A/G]GGATCCATGAGAGAA	80227
rs564184379	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884811	GCTATTACCAAACTG[A/G]TGTATTAATTGATGA	80227
rs564306572	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73900509	GCTAGTTTATTCACA[A/G]ATACACAAATAATCC	80227
rs564348245	in-del	-/AA	0.320096	0.239972	intron-variant	PAAF1	GRCh38.p7	11:73893739	TGAAACTCTGTCTCC[-/AA]AAAAAAAAAAAAAAA	80227
rs564368978	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893812	GCTTATAATCCCAGC[A/G]CTTAGGGAGACCCAG	80227
rs564408338	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73884367	AAAAAATAGCTGGGC[A/G]TGGTGGCATGCAGGC	80227
rs564487760	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893240	ATTATGAGGCTTTGG[G/T]TGTGTTCTAATGCAT	80227
rs564529474	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73906680	TTTTTAAAGCTGTGG[C/T]ATTTTCTTAAACTCA	80227
rs564668576	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913246	TGACTGGTTTCTGTT[C/T]ACCATTCAGGTCTTG	80227
rs564711994	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73889604	GGAGAAAAGTACTGA[A/T]TATTGAAATCTGTCA	80227
rs564775661	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920276	CAGTGGCTCATGCCT[A/G]TAATCCCAGCATTTT	80227
rs564812960	snp	A/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924921	ACTTTGGGAGGCCGA[A/G]ACAGGTGGATCACTT	80227
rs564858603	snp	C/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73897348	TCCTCACTTCCCAGA[C/T]GGGGTGGCTGCTGGG	80227
rs564941645	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73890538	GGAGGGAATAGGCAC[C/G]GTAAGCCTGACCCAG	80227
rs564944457	snp	C/G	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73923420	CACAAAAAAATAGAT[C/G]AAAATGTTAACAGTA	80227
rs564996181	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896950	CCCAGACCTCCCTCC[C/T]CGACGGGGCGGCTGG	80227
rs565074251	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902845	GGGATTACAGGCATG[A/C]GCCACCATGCCCGGC	80227
rs565214384	in-del	-/TA	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73908328	ATATGTGTATATATG[-/TA]TATATATGTGTATAT	80227
rs565275890	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73913168	AGGCGTGAGCCACCG[C/T]ACCTGGCCTGACTTT	80227
rs565308856	snp	G/T	0.103794	0.20279	intron-variant	PAAF1	GRCh38.p7	11:73897224	CGGGGCGGCTGGCCG[G/T]GCGGGGGGCTGACCC	80227
rs565317300	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887854	TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	80227
rs565384199	snp	A/C	1.65132e-05	0.00287339	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887427	AGAGGTTACAGCTTC[A/C]GAAGGATTTACTGTG	80227
rs565421835	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896022	GCTCAGGCAGGAGGA[C/T]CACTTGTTCCTGAGA	80227
rs565455424	snp	A/G	0.000399281	0.0141238	splice-donor-variant, intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887100	ACAGTCTGCAGAACC[A/G]TGAGCCAAATAAACC	80227
rs565481899	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73919753	TAGGAATGATGTAGG[G/T]CAGGAGGACTGGACT	80227
rs565732545	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901823	TGATCCACCAGCCTC[A/G]GCCTCCCAAAGTGCT	80227
rs565951977	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73915343	GGGCATAGTGGCTCA[C/T]GCCTGTAATCCCAGC	80227
rs565998718	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901149	TTAGTCTTTTTGGCT[A/G]AGGGAACAGTAAAAG	80227
rs566014057	snp	A/G	0.00636936	0.0560724	intron-variant	PAAF1	GRCh38.p7	11:73908273	TATATATGTGTATAT[A/G]TGTGTATATATGTAT	80227
rs566088011	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921866	TAAGTGGAAAACCAG[G/T]TTCTCCAGGAATGGG	80227
rs566089468	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73914738	GAGTCTCACTCTGTC[A/G]CCCAGGTTGGATGGA	80227
rs566150125	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73921396	CTACTTTTTGTACTT[G/T]TTTTTTTTGGAATGT	80227
rs566153062	in-del	-/AC	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73880276	GCTCTAAAAAAAGAA[-/AC]ACACACACAAATACA	80227
rs566196461	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73900075	ACCTCTATAGCTGAA[C/T]TCGAGGAAACACCTT	80227
rs566245150	in-del	-/AAAAAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73880708	AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GCCAGGCACAGCAGC	80227
rs566272222	in-del	-/A	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73919724	AGTGTACATTAAGGG[-/A]CACTGGATCCTTGTA	80227
rs566285385	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927824	CTCCCTGTTGCCTGG[C/T]CATAGAGAAGGCCTG	80227
rs566317995	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73885960	AATAAATGAATGTAG[C/T]ACCCTGCTAGACTTA	80227
rs566333865	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73892812	TACAGGTGCCTGCCA[C/T]CACGCCCGGCTAATT	80227
rs566374612	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884211	GACTTCACAAATGTA[A/G]AGAAGTCAGCTGGGC	80227
rs566480906	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911264	CTTAGCCCTAATAAT[A/C]CTCTGTACTCTGTTC	80227
rs566545441	snp	C/T	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73925376	GAGGCCAAGATGGGA[C/T]GATTGCTTGGGCCTG	80227
rs566579938	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875500	TGGGACCACAGTGGA[A/G]GGATGCCTAATCCAG	80227
rs566611530	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918599	CTCCTGCCTCAGCCT[C/G]TTTCTTTTTAGAGTC	80227
rs566664727	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881961	CTCACTGCAACCTCC[A/G]CCTCCCAGATTCAAG	80227
rs566726805	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73882883	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	80227
rs566735156	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73916953	AACTTTTAATTTTAA[A/G]GAGCTCAGTAATTTT	80227
rs566746894	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896826	GGTACACCTCCCAGA[C/T]GGGGTGGTGGCCGGG	80227
rs566816068	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73909742	TTTACTCTGTACCTA[C/G]TATGTTTCTATTACT	80227
rs566907180	in-del	-/A	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73919619	ATGCTTTACATACAT[-/A]ATTCTAGGTAAAGCG	80227
rs567039530	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73923058	TACCCATTCCCTTGC[A/G]TTCCTCAGTCTTCAT	80227
rs567090932	in-del	-/TA	0.00279273	0.0372635	intron-variant	PAAF1	GRCh38.p7	11:73908248	GTGTATATATATGTG[-/TA]TATATATGTATATAT	80227
rs567202911	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923679	TATCTGGGATTACAG[A/G]CATGCACTACCATGC	80227
rs567208889	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914218	AGTATTTTTAATTGT[A/G]TAGTTCTGTGAGTTT	80227
rs567213112	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875460	AACAGGGCAGTTTAC[C/T]ACACAGTGTACAGAT	80227
rs567272849	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874829	CGTCTCTACTAAAAA[C/T]ACAAAAATTAGGCGG	80227
rs567378872	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881853	CTAGGACTACAGGCG[C/T]GTGCTACCATGCACG	80227
rs567386096	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916226	CTCAGAAAGTTGTCA[G/T]GAAAAAGGGGCAAAG	80227
rs567400670	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886466	GGATCACGAGGTCAG[C/G]AGATCGAGTCCATTC	80227
rs567410031	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924537	CTAGTGATCTACAGA[A/T]GCAAATAAAAATACT	80227
rs567446927	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888959	TTTTACCATAACAAT[C/T]CTGTGGGATTGGCAT	80227
rs567490149	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73916348	TCAAGTCCTTAGTCA[A/G]CCCCAGGTTCCTGAA	80227
rs567520732	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922953	GATGCAAATTGCCAA[A/T]CATATCTAAAAGTAG	80227
rs567520787	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915579	CGCCACTGTACTCCA[C/G]CCTGGGGAACAAGAG	80227
rs567547845	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73893566	ACATGGCGAAACCCC[A/G]TCTCTGTTAAAAATA	80227
rs567581305	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896719	ACACAGACACGGCAA[C/G]CATCCGATTCTCAAT	80227
rs567655757	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922502	TGCCATGTGCTGTAG[A/T]GGGAGTTCTGTACTG	80227
rs567780838	snp	A/G	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73912845	TCAGTTTCTTCTTTC[A/G]GTACAGTAGACTCTC	80227
rs567809944	snp	A/T	0.0193772	0.0965046	intron-variant	PAAF1	GRCh38.p7	11:73880483	AACCCTGTCTCAGTT[A/T]AAAAAAAAAAAAAAA	80227
rs567878835	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73914795	TCACTGCAACCTCCA[A/C]CTCCTAGGTTCAAGT	80227
rs567888833	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879798	GGATCTCTTGAGCCC[A/G]GGAGGTTGAGGCTGC	80227
rs567901889	snp	C/T	0.00993419	0.0697739	intron-variant	PAAF1	GRCh38.p7	11:73883520	AGTATAATGTTTCTT[C/T]CTTTCTTTTTTTTTT	80227
rs567923335	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912093	TCCTATTTCATTGAC[A/T]GCTACTTCTTAAAGG	80227
rs567955393	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906818	AAGGTTTGTGTATCT[C/G]AAGTCATTTCATTTT	80227
rs568092088	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891636	AAAAATTAGCTGAGC[A/G]TGGTGGCACTTACCT	80227
rs568170207	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73882020	GCTGGGATTACAAGC[A/C]TGTGCCACCATGCCT	80227
rs568233235	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890809	TTTTCTTCTTAAAAC[A/G]AATGCTCTAATGCTT	80227
rs568302115	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926718	TGTCTCAAAAAACAA[A/G]CAAACAAAATTCTTG	80227
rs568329783	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73926402	CGCGCCCAGCCATCT[A/G]TTTCATTTTTAAAAA	80227
rs568364042	snp	A/G	0.000132092	0.00812579	utr-variant-5-prime, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73876984	GACTCACTTCCGGGA[A/G]GGGGCGGAAGAGGTG	80227
rs568388037	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73924289	GTGAAACCCCGTCTC[C/T]ACAAAAATTAGCCAG	80227
rs568573700	snp	C/T			downstream-variant-500B	PAAF1	GRCh38.p7	11:73927787	AAAAGTTGGTCAGGA[C/T]GATGGAATTCCTTCC	80227
rs568579770	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919614	TGTTTGATGCTTTAC[A/G]TACATATTCTAGGTA	80227
rs568627352	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910477	GACTGGGCTAGAAAG[C/T]TGAATTAAGAGGGGT	80227
rs568688758	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903959	TGTAGTGGTGTGCGC[C/T]TGTAATCCCAGCTAC	80227
rs568734274	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918513	ATGGAGTCTTGCTCT[A/G]TAGCCCAGGTTGGAG	80227
rs568751273	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73912765	ACTTTCTGACCCCTA[C/T]ACTTCTCTCCAGTCT	80227
rs568813267	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899942	GATGAGTGAAAAAGT[C/T]CCCAAGCCACCTCAG	80227
rs568856238	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73925520	CTAGAAACTTAAAAA[C/T]TTACTTTACCTCACT	80227
rs568910980	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73897593	AGATGTGATGGCGGC[C/T]GGGAAGAGGCGCTCC	80227
rs568972790	in-del	-/T	0.0133239	0.0805258	intron-variant	PAAF1	GRCh38.p7	11:73920227	AATATTTTTTATATA[-/T]TTTTTTTAATTTAAA	80227
rs569043593	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73904616	CGCCTCCAAGTAATA[A/G]GAGGTGCTTCAAGGC	80227
rs569061729	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876311	CCTAAACCAAGAGAT[A/C]CGTGTTCAAATCCCA	80227
rs569109974	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901822	GTGATCCACCAGCCT[C/T]GGCCTCCCAAAGTGC	80227
rs569226361	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875369	ATGTACCAGGCACTA[C/T]GCTAGTGCTGAGGAT	80227
rs569285315	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895221	GGAGTTGGGATGATT[C/G]AAAAAATTTTGGCCT	80227
rs569361817	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73901031	TTGTTTTCTACAATT[C/G]ATAAAGGAAAAAAAA	80227
rs569428176	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73901801	TCTCAAACTCTTGAC[C/T]TCAGGGTGATCCACC	80227
rs569443245	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73910325	AAGTTGGCTTGAACC[G/T]TTAGAGGATAAGTTG	80227
rs569490326	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73880680	TGACTGAGCAAGACT[C/G]TGTCTCGAAAAAAAA	80227
rs569554849	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924481	GGCCCACGTAATAAG[A/T]TCTATTTGCCATTCT	80227
rs569580561	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73917629	GTAACCCCAGCACTT[C/T]GGAAGGTCAAGGTGG	80227
rs569610515	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886128	TAGGATAGTATCTTA[C/T]TTAGCCCATATCTCT	80227
rs569689774	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897478	TCAGACGGGGCGGCC[A/G]GGCAGAGACGCTCCT	80227
rs569712544	snp	A/G	1.76674e-05	0.0029721	intron-variant	PAAF1	GRCh38.p7	11:73899120	TTCATTATTTCTAAC[A/G]CATTGTTTGTTTTCT	80227
rs569739511	snp	A/G	0.00438332	0.0466095	intron-variant	PAAF1	GRCh38.p7	11:73907625	ACTGCTAGATCCTGT[A/G]ACAGTACCCTACTTA	80227
rs569935427	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921744	ATCATTCTGAGGGTC[A/G]AAAACTTTCTCACAA	80227
rs569959113	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73907006	CTACTCCATACAACT[C/T]TGTGTTTTTACACCT	80227
rs570011206	in-del	-/A	0.00478085	0.0486577	intron-variant	PAAF1	GRCh38.p7	11:73894665	AAAAAAAATAAAAAT[-/A]AAAAAAAAATCAGCT	80227
rs570070164	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921359	ATGAGGAGTGTAGGT[A/G]GAGAAGAGCTGACTC	80227
rs570141283	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73927086	ATAGTCATGGTGCAT[A/C]CCAACCATTGGTGAT	80227
rs570187936	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906985	CCATAGGGTTGCACT[A/G]CCTCTCTACTCCATA	80227
rs570266997	snp	C/G	0	0	intron-variant	PAAF1	GRCh38.p7	11:73884430	ATTCTGGGAGATAGA[C/G]GCTGCAGTGAACCAT	80227
rs570310581	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880363	CAAGGAAAATACTGT[A/G]TTTTATTTTACCTAT	80227
rs570313001	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898436	GCCCAGGCTGGTCTC[A/G]AACTCCTGGGCTCAA	80227
rs570378075	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899044	GAAACACAGGCTTCA[A/G]GAAGTCTTGGAAGAG	80227
rs570465345	snp	A/C/T	6.59222e-05	0.00574085	utr-variant-5-prime, upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878812	CTGGCTGAGCTGTCA[A/C/T]CCCCCAGGTAATACC	80227
rs570543001	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877529	GTCCAGGCCCCATAC[G/T]GGATGCTTGGTGGAG	80227
rs570700602	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73921110	TTTAAGACCAGCCTG[A/G]CCAACATAGCGAAAC	80227
rs570707635	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73920638	CGGGTGGATTCCTTG[A/G]GGTCAGGAATTTGAG	80227
rs570743052	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927511	GCTGTACTGGCCGTG[C/T]GGAACTCTCATCCCA	80227
rs570816978	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898968	GGTGTTTACTTCAGC[A/C]TTGTTGGGAGGTTGG	80227
rs570900439	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73881234	ATCAACTGGGGTTTA[C/T]ATTTTTTTAGATCTT	80227
rs570937386	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874721	GGCTGGGTGCAGTGG[C/G]TCACACATGTAATCC	80227
rs570955507	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917970	GCAGTGTGATCACTT[A/G]TCTGACAGGGCTAGC	80227
rs571021799	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73898293	AACTCTTGAATCCTC[C/G]TGGTGCATCTTAGAA	80227
rs571111786	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897867	GCGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC	80227
rs571129731	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73904778	ATACACCTGGGAATA[C/T]GAAATTTGCTTTATT	80227
rs571132447	in-del	-/TA	0.00079952	0.019978	intron-variant	PAAF1	GRCh38.p7	11:73908249	GTATATATATGTGTA[-/TA]TATATATGTATATAT	80227
rs571210018	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73923123	TCTGTTAGCATTTCT[A/G]TATGTCTCTCTAAAA	80227
rs571215371	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888009	TGTCTCGGCCTCCCA[A/G]AGTGCTGAGATTACA	80227
rs571266469	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923823	TTTAAGAATTAGATA[C/T]ACTTTTACTTTCTTA	80227
rs571278450	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912253	AGTTCATGTAAAGCA[C/T]AGACCTTTCACCTGA	80227
rs571538701	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73901993	CTCAGCTTCTCAAGT[A/G]GCTGGGATCACAGGC	80227
rs571540597	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908732	CTGAATTAGCTTAGG[G/T]GTCAACTTTTTTTTC	80227
rs571605960	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902294	CGGGTACATTGAGAG[A/G]GAATAGAAACAATAT	80227
rs571679941	snp	G/T	0.00279162	0.0372561	intron-variant	PAAF1	GRCh38.p7	11:73908316	ATATATGTATATATA[G/T]GTGTATATATGTATA	80227
rs571752447	snp	C/G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889047	ATAATCAAAGACAGA[C/G/T]TGTATGCTGGAATTG	80227
rs571765787	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73886189	TACAGGTTACTGAAG[C/T]TTAATTCTTTACTAT	80227
rs571795372	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886873	CATGAATAGATTAAT[A/G]TCCTCCCTGGAGAGT	80227
rs571806092	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73894152	CTGAGGGAGAAGGCA[A/G]TTCACCTCTTGGGAG	80227
rs571832021	snp	A/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73921922	ATTTCTTTCTCACCT[A/T]GGCTTTTGGAATTGC	80227
rs571861395	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879141	ATAATTTCTAGATCT[A/T]CAGCCCCAGCCCTGA	80227
rs571899690	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73879741	AGTCAGGCATAGTGG[C/T]ATGCGCATGTAGTCC	80227
rs571905282	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922086	GTATCTGTATCTTTT[G/T]TCTCTCTGGGGGCAG	80227
rs571927826	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902009	GCTGGGATCACAGGC[A/G]TGCACCACCACATCC	80227
rs572031553	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73922538	GAAGTTGGATATAGG[C/G]CGGGCACAGTGGCTC	80227
rs572041292	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893785	AAACTAAACGTGGGC[A/G]CGGTGGCTCATGCTT	80227
rs572239139	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73928020	TATGTAGGTGAGGAA[A/G]CTGAATCATAAGCAT	80227
rs572263643	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917020	GATTGAATTATTTTT[A/T]TTTATTTATTTATTT	80227
rs572546452	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906599	TGAAAAGTTACACTA[C/T]AGTGATTAGGTCCCA	80227
rs572556797	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73913180	CCGCACCTGGCCTGA[C/T]TTTGCCTTCTTTTTC	80227
rs572696658	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926535	CAACACGGTGAAACC[C/G]TGTCTCTACTAACAA	80227
rs572710227	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73884449	GCAGTGAACCATGAT[A/C]ATACCACTGCACTCC	80227
rs572746078	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883782	CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA	80227
rs572759617	snp	C/T	0.0283406	0.115616	intron-variant	PAAF1	GRCh38.p7	11:73896941	GGCTGACCCCCCAGA[C/T]CTCCCTCCCCGACGG	80227
rs572784762	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884481	GCCTGGGTGACAGAG[C/T]GAGACCCTGTCTCAA	80227
rs572887264	snp	A/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73904097	TCAAAAAAAAAAAAA[A/G]TATATATATATACAT	80227
rs572910482	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73916739	ACATTGATTTAGCCT[A/G]GCATATAGATAACTA	80227
rs572931975	snp	C/T	0.00398564	0.0444627	intron-variant	PAAF1	GRCh38.p7	11:73926167	GCTGGAGTGCAATGG[C/T]GCGATCTCAGCCCAC	80227
rs572949598	snp	A/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73924193	GGTATGGTGGCTCAC[A/G]CTTGTAATCCCAGCA	80227
rs573046055	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902007	TAGCTGGGATCACAG[A/G]CGTGCACCACCACAT	80227
rs573051194	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73923384	TCGTTTATGCACATG[C/G]TGTCAACCATGTAAA	80227
rs573059113	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901832	AGCCTCGGCCTCCCA[A/G]AGTGCTGGGATAACA	80227
rs573156945	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73889284	CATTTGTTTCCTAAC[G/T]GCCATGAGTCACTTT	80227
rs573170099	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73886033	GTGTTATGGGCTGTT[A/C]TAGACATGAATATAT	80227
rs573187978	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908026	TTAAGTGGTCCACCA[C/T]CTTCTTTCCATCATT	80227
rs573188130	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73915659	ATTAATGAACAGACC[A/G]TTAGTTGAAGTTTCT	80227
rs573227376	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73895833	AAAGTGAGGCTGGGC[A/G]CGGTGGCTCACGCCT	80227
rs573258423	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902567	TGCACATCCAGTTTA[C/T]AAATACCTTTGGATC	80227
rs573268985	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880861	AAAAATTACCTGGGC[A/G]TGGTGGTGCATGCCT	80227
rs573363625	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902053	ATTTTTTAGTAGAGA[G/T]GGGGTTTCGCTGTGT	80227
rs573662426	snp	A/C			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874868	GCAGGCACCTGTAAT[A/C]CCAGCTACTCGGGAG	80227
rs573693073	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887650	GTGCCATCAGACTTC[C/T]TCTTACTTCCCTTAT	80227
rs573706615	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908415	GTATATATATGTGTG[-/TA]TATATATATATATGG	80227
rs573754693	in-del	-/TGC	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73905221	AGGCATTCTTGAAAT[-/TGC]TGCTTTCTTTTTTTT	80227
rs573820778	snp	C/G	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73917115	AACCTTTGCCTCCCG[C/G]GTTCAAGCAATTCTC	80227
rs573841272	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73922685	AGCCGGGCATCATGG[C/T]GGGCGCCTGTAGTCC	80227
rs574046350	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73908325	TATATATGTGTATAT[A/G]TGTATATATATGTGT	80227
rs574251694	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914005	TGGGGTGCTATGTTT[G/T]TGCTTGTGAATGGCC	80227
rs574374430	snp	A/G	0.00142074	0.0266148	intron-variant	PAAF1	GRCh38.p7	11:73919061	CCAATTGAGAGAGAT[A/G]CTTCTCTGTAGTTCA	80227
rs574437768	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911434	GTGATTCTCCCATCT[G/T]AGCCTCCCAAAGTGC	80227
rs574439336	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73882751	GGGATTACAGGTGTC[C/T]GCCACCACGCCCAGC	80227
rs574444121	snp	C/G	0.00199481	0.0315187	intron-variant	PAAF1	GRCh38.p7	11:73897976	ACTCATGGTTAGGAG[C/G]TGCAGACCAGCCCAG	80227
rs574477923	snp	A/G	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73898551	AGCAGGGCTGGGCAC[A/G]GTGGCCTATAATCCC	80227
rs574478856	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73892064	ACAGTGGCTCATGCC[C/T]GTAATCCTAGCACTT	80227
rs574515300	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73918128	CTCGGTAGAATCCCA[C/T]GTATAGAATCCCATA	80227
rs574616095	snp	A/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73891266	TCATTTTATTTGCTT[A/G]TCTAGTGCTATAAAC	80227
rs574632652	in-del	-/A	0.0240643	0.107019	intron-variant	PAAF1	GRCh38.p7	11:73880519	TGCGGTGGCTCTACT[-/A]AAAAAAAAATACAAA	80227
rs574763079	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73925898	TCTTTTCCAGAAGTA[A/G]CTAGCATTAAAAGTT	80227
rs574771910	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875763	CATCACAAGGCTTTG[C/T]AGGACATAGTAGGGA	80227
rs574794467	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923370	ATGCATAAAGACATT[C/G]GTTTATGCACATGCT	80227
rs574863860	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73920892	AAAAATAAGGTTGGG[C/T]GTAGTGGCTCACGCC	80227
rs574885032	snp	C/T	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73882256	CCTGACCTCGTGATC[C/T]GCTCCCTGGCCTCCC	80227
rs574969506	snp	A/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924891	GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGTA	80227
rs575134834	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73890044	TAAAGAGGTTCAGAA[A/C]ATTTTGATTATTGAA	80227
rs575213722	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73911381	AGAGACAGGGTCTCA[C/T]TATGTTGCCCAGGCT	80227
rs575251126	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73924265	TTTGAGACCAGCCTG[A/G]CCAACATGGTGAAAC	80227
rs575285536	snp	G/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896849	TGGCCGGGCAGAGGG[G/T]CTCCTCACTTCCCAG	80227
rs575302952	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73897955	GGAGGCCGAGGCTGG[C/T]GGATCACTCATGGTT	80227
rs575318538	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886919	CTCACTCTGTTCTTT[C/T]CTGAGAAAGCTGATT	80227
rs575420820	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73896505	GGTGATGACTCTTAA[C/G]GAGCATGCTGCCTTC	80227
rs575422841	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73903152	TTTAGTAGATTGAAC[A/G]GAATGATATACTTTA	80227
rs575429882	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73917362	CCAGCTCTGTTAGTT[A/G]TGTAGTTTTGATCAT	80227
rs575439440	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73897369	GGCTGCTGGGCGGAG[A/G]GGCTCCTCACTTCTC	80227
rs575560310	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73902636	CCAACATTCCTTAAT[C/T]CTCCCTAAGAATATG	80227
rs575683498	snp	A/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73893768	AAAAAAAAAGAAAGA[A/G]AAAACTAAACGTGGG	80227
rs575724226	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877222	GAAAAAGAAGTATCA[A/G]ACCCGTATGGTCATT	80227
rs575821552	snp	C/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73893052	TGGTATTCTATTGAT[C/G]AGTTTACTATAATTT	80227
rs575859571	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73909041	ATCCACCTGCCTCGG[C/T]CTCCCAAAGTGCTGG	80227
rs575917753	snp	A/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925013	CAAAAAAATTAGCTG[A/G]GCGTGGTGGTACATG	80227
rs575957785	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899561	AGATTACAGGCATGT[A/G]CCACCACACACATCT	80227
rs576041419	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884707	CTTCCCTGTGAAAAG[C/T]GTCTTTACTAGGTCT	80227
rs576071634	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885522	AGCCAGCTCCTATCT[C/T]TCTTTGAGGCTCCTA	80227
rs576118167	snp	C/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924745	ATTCTCATGAGAGAT[C/G]TAGGGCTTTTATGAG	80227
rs576227797	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876650	CTGAGGCGCCTCAGG[A/C]GTATCGAGGACTTTG	80227
rs576358628	snp	C/G	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73913036	CGTGCACTACCATGC[C/G]TGGCTATTTTTTGTA	80227
rs576373689	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73915116	GTTACTTAACCTCTC[G/T]GAGCCTGCTTCCTCA	80227
rs576419298	in-del	-/TTTC	0.0023933	0.0345097	intron-variant	PAAF1	GRCh38.p7	11:73926095	ATGCATATAGATCTA[-/TTTC]TTTCTTTCTTTCTTT	80227
rs576560212	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883706	ATTTTCAGTAGAGAC[A/G]AACGAGGTTTCGACA	80227
rs576638480	snp	C/T	0.000798403	0.0199641	intron-variant	PAAF1	GRCh38.p7	11:73906440	GTATTTTAGTAGAGA[C/T]GGGTTTCGCTACGTT	80227
rs576677790	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73891903	GAGGAATAATTTTCA[A/T]AGGTCTTTGTGATAT	80227
rs576684986	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73883005	CCTGGGTTCAAGAGA[A/T]CCTCCCACTTCAGCC	80227
rs576773996	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73906097	TGCAAAATAAGAAAC[A/G]AGATGGCAGCAAACC	80227
rs576839500	snp	A/C	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73899358	GTGGGACCACTCTGC[A/C]TGTCAGTTGATCTCT	80227
rs576905686	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73884606	GGCAGTTGGTAAACA[C/T]AATAGGGAATCATGG	80227
rs576929551	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876500	GCTTCAGTCTCCTCT[A/G]GAGTAAAATGACGAC	80227
rs576963104	snp	A/G			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909500	CGCTCAGCCTGCTTG[A/G]GAGTCCTTGCAGATT	80227
rs577119886	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926434	TCTTGCGTAGTGTTC[C/T]GGCCGGGCGTGGTGG	80227
rs577128388	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73919235	TGAGGGTGGTGACTG[C/T]GCCTTATTCATTGTG	80227
rs577200125	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888125	TAAATAATACTAAAA[A/G]TTATTAGAGATATTT	80227
rs577264673	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73926008	ATCTTCAGTTTGTAC[A/G]TAATTGAGACTATCT	80227
rs577343634	snp	C/G	0.00159617	0.0282053	intron-variant	PAAF1	GRCh38.p7	11:73895975	ATTAGCTGGACATGC[C/G]AGCCCATGTTTGTAA	80227
rs577362947	snp	A/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73890885	TTTCAACACAAAAAG[A/T]TAATGGCATCTTAGC	80227
rs577439638	snp	A/G	0.0197687	0.0974348	intron-variant	PAAF1	GRCh38.p7	11:73897282	CTGGCCGTGTGGGGG[A/G]CTGACCCCCCCACTT	80227
rs577499689	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73897874	GAGATCACACCACTG[C/T]ACTCCAGCCTGGGGC	80227
rs577500614	snp	A/G	0.00119737	0.0244387	intron-variant	PAAF1	GRCh38.p7	11:73890456	CTAGGTAGAACACAT[A/G]GGGCATCAAAATATA	80227
rs577650481	in-del	-/ATT	0.00318978	0.0398085	intron-variant	PAAF1	GRCh38.p7	11:73891727	CTGCAGTGAGCTGAG[-/ATT]ATGCCACTGCACTGC	80227
rs577778258	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73911187	GGTGTTATATATCCT[A/G]TAGGGTCTGACAAGT	80227
rs577853726	snp	C/T	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73923147	TCTAAAAGACAAGGA[C/T]TCATTTTTGGAGAAG	80227
rs577896229	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	PAAF1	GRCh38.p7	11:73927860	CAGTAGCAATAAATG[A/T]CCTGTAAGCTGCCAC	80227
rs578036899	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73914777	GCGCAATCTCGGTTC[A/G]GCTCACTGCAACCTC	80227
rs578112910	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73913939	CCTGTAGTCCCAGCT[A/G]CTCAGGAGGCTGAGG	80227
rs578166299	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73885372	TGGTCTTGAACTCCT[A/G]ACCTTGTGATCCACC	80227
rs578177920	snp	A/G	0.000399281	0.0141238	intron-variant	PAAF1	GRCh38.p7	11:73907700	GGCTTCCATGGGAGC[A/G]GGGTAGATGATCACC	80227
rs578241325	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877813	ATCGGTTGAACCCAG[A/G]AGGTGGAGGTTGCAG	80227
rs578250752	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878568	TTAACCAACAGATAT[A/C]TATTCATTAAATAGT	80227
rs745366136	snp	C/T	1.64993e-05	0.00287218	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887420	GCATCCCAGAGGTTA[C/T]AGCTTCAGAAGGATT	80227
rs745438074	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875283	CACCATGATGGGCTG[C/T]AAAGCAACTAGGACT	80227
rs745532906	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73914079	AAAAGTACACACACA[C/G]ACAGGCACATTTTAA	80227
rs745536658	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73879691	GGCAACAAAGTGAGA[A/C]CCCCTCCCCATCTCT	80227
rs745753040	snp	C/T	1.64904e-05	0.00287139	intron-variant	PAAF1	GRCh38.p7	11:73914399	GTTATTAACATAGTT[C/T]ATTTGTCATGCAGGT	80227
rs745756906	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887969	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG	80227
rs745769421	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73890448	GATAATGACTAGGTA[C/G]AACACATGGGGCATC	80227
rs745807880	snp	A/G	1.66369e-05	0.00288412	intron-variant	PAAF1	GRCh38.p7	11:73914522	AAGTGGTTCCTATAT[A/G]ACCTTTGAACTCTGA	80227
rs745808276	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73886138	TCTTACTTAGCCCAT[A/C]TCTCTGCAAAATCAG	80227
rs746001860	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73895854	GCTCACGCCTGTGAT[A/C]CTAGCACTTTGGGAG	80227
rs746034538	snp	G/T	1.64844e-05	0.00287087	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918967	CTCCGGTACAAGTCA[G/T]CCACAGATCAGGAGC	80227
rs746056722	in-del	-/G	3.42179e-05	0.00413615	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927396	CCCGGTTAGTGAAAA[-/G]GTTTGACCCTGATCA	80227
rs746091940	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899192	GTCTTGGTGTGTCTT[C/T]TAGTACTGACGGGAC	80227
rs746097625	snp	C/T	3.34191e-05	0.0040876	intron-variant	PAAF1	GRCh38.p7	11:73924582	TGGATGCAGTTTTCT[C/T]TTAGTTATATGAATT	80227
rs746103116	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913049	GCCTGGCTATTTTTT[A/G]TATTTTTAGTAGAGA	80227
rs746342502	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909440	CGGGGGAGGAATGTG[A/G]TGTCTGCTTCTCGAG	80227
rs746351068	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926737	ACAAAATTCTTGTGT[A/G]GTGTTCCATATTTTG	80227
rs746362925	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890997	AGGAGAACGAGAGAG[A/G]GTACACTGAGAAGAT	80227
rs746392627	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73898384	ATTTTTTATATTTAC[G/T]TTAAAATTTTTTGTA	80227
rs746443798	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73915457	AATACAAAAAATTGG[C/G]TGGGCATGGTGGCAT	80227
rs746570638	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877834	GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG	80227
rs746626308	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73882107	GCTGGTCTCGAACTC[C/G]CAACCTCAGGTGACC	80227
rs746651103	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73903321	TGATAGCTTAACAGC[A/G]TATATATAGATAGAT	80227
rs746668545	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902639	ACATTCCTTAATTCT[C/T]CCTAAGAATATGTAT	80227
rs746724397	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73910857	TAGTTGGGTGTGGTA[G/T]TGTGTGCATGTAATC	80227
rs746762852	snp	A/G	3.34818e-05	0.00409143	missense, synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899242	TCCAATGGAGAACTC[A/G]GGGTAAAGGATTTGG	80227
rs746823899	in-del	-/TG			intron-variant	PAAF1	GRCh38.p7	11:73908356	ATATATGTGTATATA[-/TG]TGTGTATATATATAT	80227
rs746840324	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73892902	CCTGACCTTGTGATC[C/T]GCCCACCTCGGCCTC	80227
rs746884363	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888131	ATACTAAAAATTATT[A/G]GAGATATTTTACATT	80227
rs746944830	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73926713	GAGTCTGTCTCAAAA[A/C]ACAAACAAACAAAAT	80227
rs746987722	snp	A/G	4.94328e-05	0.00497131	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909558	TGGGTGCTGCTGACA[A/G]CTCCATAAACCTTGG	80227
rs747125170	in-del	-/TGC			intron-variant	PAAF1	GRCh38.p7	11:73881654	TGTTGTTGTTGTTGT[-/TGC]TGTTGTTTTAAATTA	80227
rs747167389	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73921743	TATCATTCTGAGGGT[C/G]GAAAACTTTCTCACA	80227
rs747173122	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73900620	TTGAACTGTCTTACA[C/T]AGTTGGTTTGATACC	80227
rs747199316	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906541	CAGTTGTGAGGCACT[A/G]TACCTGGCCTGGATT	80227
rs747230387	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73915911	ATTTTTGCTAATATC[A/G]CCTTTGTACTTGAGT	80227
rs747241518	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73883773	TGATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT	80227
rs747275280	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73920148	AAACTGATTAAGGGC[A/G]TATGGGAACCTTCTG	80227
rs747283483	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890902	AATGGCATCTTAGCA[A/G]TACCAAATTACACTG	80227
rs747324320	snp	A/C/G	3.34036e-05	0.00408667	intron-variant	PAAF1	GRCh38.p7	11:73916671	CCAAGGTGAGTCACC[A/C/G]TTCATTTACATGATG	80227
rs747342025	snp	C/T	1.65105e-05	0.00287315	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927308	ATGGGAGAAGCAGAT[C/T]TACACATGCTGTCGA	80227
rs747355997	in-del	-/A			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925156	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	80227
rs747429963	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73907718	GTAGATGATCACCTC[C/T]TGTTCAGCCCCACTG	80227
rs747442423	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73898541	AAAATAAAATAGCAG[A/G]GCTGGGCACGGTGGC	80227
rs747455089	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73895717	GGAGCATTTGCAGCT[-/G]GTTGTTTTTTAATAA	80227
rs747463138	snp	A/G	1.66427e-05	0.00288462	stop-lost, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927362	GCTTTCTGACCTCTG[A/G]CTTCTTGGAAAGAGC	80227
rs747463313	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893921	AAAGTTAGCCAGGTA[C/T]GGTGATGTACATCTG	80227
rs747467314	in-del	-/TG	1.71838e-05	0.00293114	intron-variant	PAAF1	GRCh38.p7	11:73914555	CAACCTGGGTCACTC[-/TG]TGTCTTAGAAAGCTA	80227
rs747497342	snp	C/G			utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73877018	TGGTGGAGGCGGGGT[C/G]GAGATGGCGGCGCCT	80227
rs747542047	in-del	-/TATA			intron-variant	PAAF1	GRCh38.p7	11:73893374	TATTATTTTTGAAAT[-/TATA]TAAATTAATTAAATC	80227
rs747605221	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917802	CTTGAACCTGGGAAG[C/T]GGAGGTTGCAGTGAG	80227
rs747605466	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73903448	TGGTCCGGGCACTGT[A/G]GCTCATGCCTGTAAT	80227
rs747754238	snp	G/T	8.2558e-05	0.00642434	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909543	TCAATGGAGTGGCGG[G/T]GGGTGCTGCTGACAA	80227
rs747795949	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73926801	CTGGGGCCTGGGGGG[C/T]TGAGAAAGTTGCCCT	80227
rs747809178	snp	C/T	1.65236e-05	0.00287429	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878755	TTTGGGTAAGCCTAA[C/T]TAGGCTTTTGTCTTT	80227
rs747817969	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73889351	TAGATCTGTCATTAT[A/G]CTTAAATGTCTAACC	80227
rs747881538	snp	A/G			downstream-variant-500B	PAAF1	GRCh38.p7	11:73928004	ATGATTGGTCAGCCT[A/G]TATGTAGGTGAGGAA	80227
rs747893587	in-del	-/AG			intron-variant	PAAF1	GRCh38.p7	11:73901089	TGTGCTGGGAAATAG[-/AG]AGAGAGAGTGAGAGA	80227
rs747953307	snp	C/T	1.8643e-05	0.00305305	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891117	CTTTGTTTAGAAAAG[C/T]ATTCATATTTCATGT	80227
rs747980877	in-del	-/TTTAGT			intron-variant	PAAF1	GRCh38.p7	11:73923484	TGTACCTCTGCTTTG[-/TTTAGT]TTTAAAGTTTTGTTC	80227
rs747988835	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906323	AGTGGTGCAATCTCC[A/G]CTCACTTCAACCTCT	80227
rs747999268	snp	A/C	3.64538e-05	0.00426914	intron-variant	PAAF1	GRCh38.p7	11:73899107	GGAATAAGAGTATTT[A/C]ATTATTTCTAACACA	80227
rs748066777	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912425	AGCCTGAGATTCACT[C/T]ACAGTCCACCCTCTC	80227
rs748154777	snp	C/G	1.65078e-05	0.00287291	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900342	CTTGTGGTCCTGAGT[C/G]GGGGAATGGATGCCC	80227
rs748192595	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921882	TTCTCCAGGAATGGG[A/G]AAGTTAGTGATTCCC	80227
rs748287594	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909078	AGGTGTGAGCCACCA[C/T]GCCCGACCTCTTAAT	80227
rs748341913	in-del	-/AAAAAAAAAAAAA			intron-variant	PAAF1	GRCh38.p7	11:73893739	TGAAACTCTGTCTCC[-/AAAAAAAAAAAAA]AAAAAAAAAAGAAAG	80227
rs748412835	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73894613	TTGTGCACGTGTACC[C/G]TAAAACTTAAAGTAT	80227
rs748510912	snp	C/T	1.64817e-05	0.00287064	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878814	GGCTGAGCTGTCATC[C/T]CCCAGGTAATACCCA	80227
rs748607662	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879455	TTCTTTTCAAATTGT[A/G]ACCGAGGTGGTACCA	80227
rs748640255	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924635	GGAAGCTGTTTTATT[A/G]TCCAGCAAGACTTAG	80227
rs748659007	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73895595	CAAAGTAAAATGGAA[A/C]GTTGGATAATTAAAG	80227
rs748661918	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73916744	GATTTAGCCTAGCAT[A/G]TAGATAACTATTGAA	80227
rs748669900	snp	A/G	3.30644e-05	0.00406585	splice-acceptor-variant	PAAF1	GRCh38.p7	11:73927284	AATTCTTGTGTTTTA[A/G]GTAGCCACATGGGAG	80227
rs748693157	snp	A/G	8.81127e-05	0.00663691	intron-variant	PAAF1	GRCh38.p7	11:73900239	GGGATGGACAAGAGA[A/G]CTAGCATGGAATTTT	80227
rs748778602	snp	C/T	1.69599e-05	0.00291199	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927383	TGGAAAGAGCAGTCC[C/T]GGTTAGTGAAAAGGT	80227
rs748808940	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73906273	TTTGTTTGTTTGTTT[G/T]TTTGAGATTCCCTCT	80227
rs748843987	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73923896	CAGATTGAGGAATAA[-/T]CTGGGAACATTTTAA	80227
rs748896577	snp	A/G	4.94205e-05	0.0049707	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909453	TGGTGTCTGCTTCTC[A/G]AGATGGGACAGCACG	80227
rs748901071	snp	C/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875186	CTGTCTTGCCCGTCT[C/G]CATCAGAACACTCAG	80227
rs748902487	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73901198	CATCATCAGACATTA[C/T]GATAGAGCTTGATGA	80227
rs748937042	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73912567	GGTCCAAACTATCAT[C/G]ATCTATTGCCTGTAC	80227
rs749135118	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876732	CCCGCAACGCCTCCT[G/T]AAGAACGCGGTACGC	80227
rs749159385	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73883877	GTAATACTCTGTTGT[A/T]TGGATATACTACATT	80227
rs749181405	snp	A/G	3.30426e-05	0.0040645	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887430	GGTTACAGCTTCAGA[A/G]GGATTTACTGTGAAT	80227
rs749183330	snp	A/G	3.3145e-05	0.0040708	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916659	GATGTGAGGAGTCCA[A/G]GGTGAGTCACCATTC	80227
rs749236315	snp	A/T	2.16064e-05	0.00328675	intron-variant	PAAF1	GRCh38.p7	11:73891083	GGAGGAGTTTTACTG[A/T]TGAATCTCATCTTTT	80227
rs749307642	snp	A/C/T	3.30424e-05	0.00406452	intron-variant	PAAF1	GRCh38.p7	11:73924600	AGTTATATGAATTTT[A/C/T]TTTCTGCCTTTCAGG	80227
rs749384075	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73894886	CTGCTCGAGAGGCTG[C/G]GATGGAAGGATTGCT	80227
rs749412406	in-del	-/T	0.000116071	0.00761721	intron-variant	PAAF1	GRCh38.p7	11:73909382	CTCCATCTTAGGGAG[-/T]TTTTTTCTCTTGCTA	80227
rs749442611	in-del	-/TATATATATGTA			intron-variant	PAAF1	GRCh38.p7	11:73908248	GTGTATATATATGTG[-/TATATATATGTA]TATATGTGTATATAT	80227
rs749556251	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73911136	TGACACATTATTGTC[A/C]CCCAAAGTTCAGAGT	80227
rs749608285	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73881229	AAAACATCAACTGGG[G/T]TTTATATTTTTTTAG	80227
rs749613115	in-del	-/AAAAAAAGAAAA			intron-variant	PAAF1	GRCh38.p7	11:73913692	ATAGAAGATGAGGGT[-/AAAAAAAGAAAA]AAAAAAAGAAAAAAA	80227
rs749650410	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909531	GTGGTTCTTCTATCA[A/G]TGGAGTGGCGGTGGG	80227
rs749701222	snp	C/T	1.65562e-05	0.00287712	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878736	CTATGGGATCCTATT[C/T]AACTTTGGGTAAGCC	80227
rs749775025	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73904902	TTTTCTTGAAGGCAA[A/T]TGCTTTTGTGTTCTG	80227
rs749919994	snp	A/G	1.64921e-05	0.00287155	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916628	TGGGACTCAAGATGG[A/G]AACATTTATCAGCTG	80227
rs749975168	snp	A/G	1.71182e-05	0.00292554	intron-variant	PAAF1	GRCh38.p7	11:73918916	ATTGCTTTTGAAGAA[A/G]GAAAGTAAAATTTCC	80227
rs750000396	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73895185	GCTGATGACTTGGAT[C/G]TTAAGTATGAGAGAA	80227
rs750053963	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877706	GCCTGACCAACATGG[C/T]GAAACTCCGTCTCTA	80227
rs750088030	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909894	CATTGGAAGACTTGT[C/T]TTGGGCCACACATAA	80227
rs750109971	snp	A/C	2.08266e-05	0.0032269	intron-variant	PAAF1	GRCh38.p7	11:73891216	TGTAAGTATTTTGAT[A/C]AAATGAAGAGAAAAT	80227
rs750239029	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73916294	GTTGAGTGGTAGTAG[C/T]TGGAAAACTGCTACT	80227
rs750308761	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73904553	CAGTATCAGCACTTG[C/T]GCCATTATTTTCCAA	80227
rs750492230	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876035	CTGGGAGGCTGAGGC[A/G]GGAGGATGGTTTGCG	80227
rs750512470	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891504	TGCTTGGCTAGGTGC[A/G]GTGGCTCACACCTGC	80227
rs750635279	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878672	CTATCTCATGTCTAA[A/G]TACTATGACCAAGCT	80227
rs750685355	snp	G/T	1.65214e-05	0.0028741	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899178	TTCCAGCAGAGGAGG[G/T]CTTGGTGTGTCTTCT	80227
rs750695464	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914120	GGATTTACTGAGGTA[C/T]CTTTTACATATGGTA	80227
rs750761480	snp	C/T			missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887099	TACAGTCTGCAGAAC[C/T]GTGAGCCAAATAAAC	80227
rs750905005	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73923021	AACTTAAGCTATTAT[C/G]AATATATTGCTAATC	80227
rs750905709	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909517	AGTCCTTGCAGATTG[C/T]GGTTCTTCTATCAAT	80227
rs750922728	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887220	CACCTGACTTTTAAC[A/C]CAGGCACCTGTTTTT	80227
rs751137146	snp	A/G	1.65696e-05	0.00287828	intron-variant	PAAF1	GRCh38.p7	11:73914511	AGGCAGCTGGCAAGT[A/G]GTTCCTATATGACCT	80227
rs751140307	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73895321	AAATAAAAGTTTTCT[C/T]TGGACATGTTCAGTT	80227
rs751226382	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73898650	GGTGAAACTCTGTCT[C/G]TACCGAAAAATACAG	80227
rs751233876	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917710	AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA	80227
rs751234829	snp	C/T	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916613	CTTCTTGCTATTGGC[C/T]GGGACTCAAGATGGA	80227
rs751242886	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879324	ATTTCTTAAGTTACC[A/G]TCATTTTTCTAGGCA	80227
rs751344512	in-del	-/ATTTTTC	2.46703e-05	0.00351206	intron-variant	PAAF1	GRCh38.p7	11:73891245	TGTAATAGCATGTTA[-/ATTTTTC]ATTTTTCATTTTATT	80227
rs751389405	snp	A/C	1.71264e-05	0.00292624	intron-variant	PAAF1	GRCh38.p7	11:73927235	GCCTCCATCTTTTTG[A/C]AATGGAAGAATCCCA	80227
rs751442580	snp	A/G	4.95405e-05	0.00497673	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927322	TCTACACATGCTGTC[A/G]AGACGGTCTTGTACG	80227
rs751469770	in-del	-/GAGGGA			intron-variant	PAAF1	GRCh38.p7	11:73898218	GGGGAGGGGAAGGGG[-/GAGGGA]GAGGGAGAGGGAGAG	80227
rs751486523	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73894538	CTAATGTTAAATGAC[A/G]AGTTAATGGGTGCAG	80227
rs751512100	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73925742	TAATCTTTGTTACTA[A/T]TTGTTGAGGTGTAGG	80227
rs751629541	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909426	CAGCCATCGTTGATC[A/G]GGGGAGGAATGTGGT	80227
rs751640575	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877433	ACCACTTTGTGTATG[C/T]GATGGAACCTTTGTA	80227
rs751674448	snp	C/G	0.000197661	0.00993939	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909501	GCTCAGCCTGCTTGG[C/G]AGTCCTTGCAGATTG	80227
rs751682487	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908361	GTGTATATATGTGTG[-/TA]TATATATATATGTAT	80227
rs751756694	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902790	CAACCTCTGCCTCCT[C/T]GGTTCAAGCAATTCT	80227
rs751786529	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73885712	CCAGGTGTGGTGGCA[C/T]GTGCCTTTAATCCCA	80227
rs752011822	snp	A/G	4.95675e-05	0.00497808	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887355	TTTGTACCATATAGG[A/G]AAACCATCTTTGTAT	80227
rs752037930	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73926091	GGTAAATGCATATAG[A/C]TCTATTTCTTTCTTT	80227
rs752065097	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908892	CTCCCAGGTTCGAGC[A/G]ATTCTCCTGCCTCAG	80227
rs752148085	snp	C/T	5.01316e-05	0.00500632	synonymous-codon, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900293	GGAAGGACATGTGTT[C/T]GATGTGAATTGTTGC	80227
rs752167580	in-del	-/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888833	TTCTCTGAGTCTCAG[-/T]TTTCCTCATCAATAA	80227
rs752211300	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73912325	TACCTTGTCTAACAA[A/G]GAGTGTTTGATCCCT	80227
rs752247001	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73881032	TAAAATAAAAATACA[C/T]AAAAGACCTACATTT	80227
rs752378442	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73921003	CAGGCCATTTTACTG[A/T]TTATTAACATCTCTG	80227
rs752431563	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919531	TGCAAAGTCATAGAT[A/G]AGGCAAGCGGGGGCA	80227
rs752467461	snp	A/C	3.29658e-05	0.00405978	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878788	TCGTAGGAAGGATGA[A/C]GGGGAGGCCTGGCTG	80227
rs752624408	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876479	CTCTCCTCTCACCAC[C/T]TTTTGGCTTCAGTCT	80227
rs752637138	snp	A/G	0.000116074	0.00761731	intron-variant	PAAF1	GRCh38.p7	11:73919076	GCTTCTCTGTAGTTC[A/G]GTTAATTAAACATAG	80227
rs752643047	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876298	AAAGTGCCTTGATCC[C/T]AAACCAAGAGATCCG	80227
rs752654262	in-del	-/T	4.95618e-05	0.00497779	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899178	TTCCAGCAGAGGAGG[-/T]CTTGGTGTGTCTTCT	80227
rs752674853	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899613	GATGGGCTTTCGCCA[C/T]GTCGGCCAGGCTGGT	80227
rs752694361	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891593	CCAGCCTGGGCAACA[A/G]AGTGAAACCCTGTCT	80227
rs752705181	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73883923	TCAATTAATGGACAC[A/T]TATTTCTAGTTTTTG	80227
rs752843931	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902900	GAGACTGGGTTTCAC[C/T]ATATTGGCCAGGCTG	80227
rs752927122	snp	C/G	1.72062e-05	0.00293306	intron-variant	PAAF1	GRCh38.p7	11:73900450	TTCTCCAAAAGGCTT[C/G]TCTAATGATCCCCAG	80227
rs752927798	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73904260	CTAAAAGTAGTTTTG[C/T]GATTGTAACATATGA	80227
rs752948987	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73922772	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	80227
rs753100261	snp	A/G	3.29636e-05	0.00405964	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914467	TGGCCCGGGAAGATA[A/G]GAAACTTCAGTGCTT	80227
rs753155466	snp	A/G	1.65644e-05	0.00287783	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887348	TGCTTCTTTTGTACC[A/G]TATAGGGAAACCATC	80227
rs753155492	snp	A/C	1.6492e-05	0.00287154	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916565	CCTCTTTATTGGCTC[A/C]GACGCTTTCAACTGC	80227
rs753195137	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73909604	GCCCAGTAAGTTGAT[A/G]ATGATATGTAGCATT	80227
rs753225864	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73904867	TTGGCTGGGATGCTC[A/G]TATGTGATTCTGCTG	80227
rs753227553	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73890290	ACCTCTACACGTGCT[A/T]CCTTCAAACGCCAAT	80227
rs753274099	snp	C/T	1.65119e-05	0.00287327	intron-variant	PAAF1	GRCh38.p7	11:73919050	GGGTCCATGGGCCAA[C/T]TGAGAGAGATGCTTC	80227
rs753281810	snp	C/T	0.000282845	0.0118888	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889095	TTCCAAGTTTAGCAC[C/T]ACCATGCAAGCCTAC	80227
rs753380716	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73908724	TTTTCAAACTGAATT[A/T]GCTTAGGTGTCAACT	80227
rs753434180	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884466	TACCACTGCACTCCA[A/G]CCTGGGTGACAGAGC	80227
rs753466853	in-del	-/CT			intron-variant	PAAF1	GRCh38.p7	11:73891603	CAACAGAGTGAAACC[-/CT]GTCTCCACAAAAAAA	80227
rs753601019	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73901653	TGTCGCCTAGGCCGG[A/T]GTCCAGTGGCATGAT	80227
rs753665283	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909488	TGGGATTGTGGGCGC[C/T]CAGCCTGCTTGGGAG	80227
rs753672835	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877589	GGTTCCTGCTCTTCA[A/G]GAAGCTGACATCCAG	80227
rs753718658	snp	C/T	0.000135217	0.00822134	utr-variant-5-prime, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73876971	CACGCTTCTCGGGGA[C/T]TCACTTCCGGGAAGG	80227
rs753757776	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73916006	CCTTTTCTTTTTAGT[A/G]TGTTTGGGGAAGACA	80227
rs753780250	snp	G/T	1.6821e-05	0.00290004	intron-variant	PAAF1	GRCh38.p7	11:73918928	GAAAGAAAGTAAAAT[G/T]TCCCCTTTCTCTGAA	80227
rs753802511	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914835	GCATCAGCCTCCTGA[A/G]TAGCTGGGATTACAA	80227
rs753806778	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73915115	AGTTACTTAACCTCT[C/T]TGAGCCTGCTTCCTC	80227
rs753808574	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878245	CAGCACCAGAATCAG[A/G]AGGCTTAATTTGCCC	80227
rs753826250	in-del	-/TGT			intron-variant	PAAF1	GRCh38.p7	11:73881642	CAACAAACTTAATGT[-/TGT]TGTTGTTGTTGTTGT	80227
rs753892889	in-del	-/C	0.00227535	0.0336526	intron-variant	PAAF1	GRCh38.p7	11:73924604	ATATGAATTTTCTTT[-/C]TGCCTTTCAGGTGAT	80227
rs753949097	snp	C/T	2.3807e-05	0.00345006	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887312	GAGAAAAATAATAAA[C/T]TTTTCTTATTTTTTG	80227
rs753958710	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73905310	CTCAGTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	80227
rs753987185	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73920239	ATATTTTTTTAATTT[-/A]AAAAAACAAGTAGGC	80227
rs754002765	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926486	GGCGGAGGGGGTGCG[A/G]ATCACGAGGTCAGGA	80227
rs754021347	snp	A/G	4.95577e-05	0.00497759	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927327	ACATGCTGTCGAGAC[A/G]GTCTTGTACGACGCT	80227
rs754025358	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899853	TCAGTGATCCATTTC[C/T]AAGACAGAATAGCTT	80227
rs754053510	snp	C/T	3.36157e-05	0.0040996	intron-variant	PAAF1	GRCh38.p7	11:73927259	AATCCCAGGCTTCCT[C/T]TGAACTGTGAATTCT	80227
rs754087218	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73912151	ACCTTTAAATACTAG[A/C]GGGCCCCACTATTAA	80227
rs754291397	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73885106	CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	80227
rs754294044	in-del	-/TTAT			intron-variant	PAAF1	GRCh38.p7	11:73882436	TTATTTTTATTTTTA[-/TTAT]TTATTTATTTATTTA	80227
rs754311438	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73900170	CAGCATGTGGGTTTA[G/T]CATGTAGGTATTTCA	80227
rs754315940	snp	A/G	3.29609e-05	0.00405948	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878811	CCTGGCTGAGCTGTC[A/G]TCCCCCAGGTAATAC	80227
rs754381349	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879379	GACCCTGCCATATCC[A/G]GGAAGCTCCCAAGTC	80227
rs754382858	snp	A/C	1.64808e-05	0.00287057	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914457	ATGCTGCTCTTGGCC[A/C]GGGAAGATAAGAAAC	80227
rs754539696	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73907942	TGCAGTGTCCTGTCC[A/T]GGACATGTGGGAGGC	80227
rs754691703	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73905895	TTTGAAATAGTGGTT[A/G]GAACTTCCAGTAGAG	80227
rs754717074	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917742	CTGGGCATGGTGGCA[C/T]GTACCTATAATCCCA	80227
rs754726989	snp	C/T	5.08884e-05	0.00504397	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909540	CTATCAATGGAGTGG[C/T]GGTGGGTGCTGCTGA	80227
rs754766252	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73889251	GGTTCAGACAGTAAG[A/T]GCTTATGGTTGAACA	80227
rs754783589	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894551	ACGAGTTAATGGGTG[C/T]AGCACACCAGCATGG	80227
rs754810940	in-del	-/AG	1.83382e-05	0.003028	intron-variant	PAAF1	GRCh38.p7	11:73899098	TATTTCAAGGGAATA[-/AG]AGTATTTCATTATTT	80227
rs754835251	snp	A/G			intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919306	CTTAAAGGAGCTCAC[A/G]GTAAGGCAGACAGAC	80227
rs754867830	snp	C/T	1.67736e-05	0.00289595	intron-variant	PAAF1	GRCh38.p7	11:73918930	AAGAAAGTAAAATTT[C/T]CCCTTTCTCTGAATC	80227
rs754907696	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73896730	GCAACCATCCGATTC[A/T]CAATCTTTTCCCCAC	80227
rs754909946	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874847	AAAAATTAGGCGGGC[A/G]TGATGGCAGGCACCT	80227
rs754923617	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73890591	CCATAATTTACTTTA[C/G]CAATTTCATCTGGTC	80227
rs754939986	snp	A/C			downstream-variant-500B	PAAF1	GRCh38.p7	11:73927950	GTTTTCTGTGACTTG[A/C]AACTTTCAATGCCAA	80227
rs754958028	snp	G/T	1.83216e-05	0.00302662	intron-variant	PAAF1	GRCh38.p7	11:73899101	TTCAAGGGAATAAGA[G/T]TATTTCATTATTTCT	80227
rs754990230	snp	A/T	1.65291e-05	0.00287476	intron-variant	PAAF1	GRCh38.p7	11:73919060	GCCAATTGAGAGAGA[A/T]GCTTCTCTGTAGTTC	80227
rs755036287	snp	G/T	5.03723e-05	0.00501833	intron-variant	PAAF1	GRCh38.p7	11:73927260	ATCCCAGGCTTCCTT[G/T]GAACTGTGAATTCTT	80227
rs755064556	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914895	ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT	80227
rs755150859	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887515	TGGTAGTACCCAAAC[A/G]TCTACCTTAGATATT	80227
rs755161935	snp	C/G/T	3.30618e-05	0.00406571	missense, stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927336	CGAGACGGTCTTGTA[C/G/T]GACGCTACCAGCTTT	80227
rs755288982	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909045	ACCTGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	80227
rs755416996	snp	A/G	1.66335e-05	0.00288383	intron-variant	PAAF1	GRCh38.p7	11:73909615	TGATAATGATATGTA[A/G]CATTGTTTTATTTTC	80227
rs755496093	snp	C/T	5.6879e-05	0.00533257	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887322	ATAAATTTTTCTTAT[C/T]TTTTGAGACATGCTT	80227
rs755649177	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73912470	ACATCAGCAAAGTCT[A/G]TCATCTCTAACTTCA	80227
rs755652415	snp	A/G	1.71015e-05	0.00292411	intron-variant	PAAF1	GRCh38.p7	11:73918917	TTGCTTTTGAAGAAA[A/G]AAAGTAAAATTTCCC	80227
rs755655278	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73917995	GCTAGCTACAGAAAT[A/C]TAAGGAAGCACCAAA	80227
rs755663607	snp	C/G	1.6501e-05	0.00287232	intron-variant	PAAF1	GRCh38.p7	11:73891226	TTGATAAAATGAAGA[C/G]AAAATGTAATAGCAT	80227
rs755666761	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73889637	TAGCTCCAAAGAAAT[-/G]AAGTCTTCTGAGAGC	80227
rs755699975	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887254	TCGTGGGCCAATTTC[A/C]TGGGTATACTATTTA	80227
rs755754910	in-del	-/A			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875666	TCTGACACATGAGAG[-/A]CAAAAAAAAAAAAAA	80227
rs755799652	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73917870	GCGAGACTCTATCTC[-/A]AAAAAAAAAAAAAAA	80227
rs755819556	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73907254	CTCGATCTTAATTCC[A/G]TCATCTTTTTTGGCA	80227
rs755875274	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73906229	AACAACCGTTGCCAG[C/G]TGTATAAATTGAATT	80227
rs755960728	in-del	-/A/TA	1.64757e-05	0.00287012	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924648	TGTCCAGCAAGACTT[-/A/TA]AGACTATGTCACTGA	80227
rs756012279	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874812	CCGGGATGATGAAAC[C/T]CCGTCTCTACTAAAA	80227
rs756028210	snp	A/C			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876342	GCACTACGCCTTACT[A/C]TGTAATCTTTTTCAT	80227
rs756065269	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876528	GACGACCCCTGCTCA[C/G]AGATCAGGGTAGGCT	80227
rs756091196	snp	C/T	3.29902e-05	0.00406128	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916631	GACTCAAGATGGAAA[C/T]ATTTATCAGCTGGAT	80227
rs756122360	in-del	-/AG	1.72225e-05	0.00293444	splice-acceptor-variant, intron-variant	PAAF1	GRCh38.p7	11:73900268	TTCTTTTGTTTTTCC[-/AG]AGAGTATTGGAAGGA	80227
rs756242252	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73923593	CAGGCTGGAGTGCAG[C/T]GGCACCATCTTGGCT	80227
rs756394623	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73895660	GGGAATTATTGTTGC[C/T]GGGAATGTGTCTGGA	80227
rs756403863	snp	A/T	5.00388e-05	0.00500169	intron-variant	PAAF1	GRCh38.p7	11:73924585	ATGCAGTTTTCTCTT[A/T]GTTATATGAATTTTC	80227
rs756451968	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73910867	TGGTAGTGTGTGCAT[A/G]TAATCCCAGCTACTC	80227
rs756456740	snp	C/T	5.13027e-05	0.00506445	intron-variant	PAAF1	GRCh38.p7	11:73927238	TCCATCTTTTTGAAA[C/T]GGAAGAATCCCAGGC	80227
rs756465474	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912081	CACTGGTTTTCTTCC[C/T]ATTTCATTGACTGCT	80227
rs756475037	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73926458	GTGGTGGCTCATGCC[C/T]AGCACTTTGGGAGGC	80227
rs756482117	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877086	GAATCCAGGCCCAGA[A/G]CAGAGTCAGAGGAGG	80227
rs756533670	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73907309	ATGAGGGCTGGGTAG[A/G]TAAGAATGTTCAGCC	80227
rs756592712	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73884025	GGGGTGAAAGGATTA[C/T]AAAACTGCTGAGTTT	80227
rs756602398	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73880909	GAAGGCTGAGGCAGG[A/T]GAATCGCTTAAACCC	80227
rs756607040	snp	C/G			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914431	AACGGGAGGTTGGAA[C/G]AGAGGCCAAAATGCT	80227
rs756635801	snp	A/G	1.65512e-05	0.00287669	intron-variant	PAAF1	GRCh38.p7	11:73909605	CCCAGTAAGTTGATA[A/G]TGATATGTAGCATTG	80227
rs756680014	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73907420	GGAAGTTCAGCTTCC[C/G]CCTTGGTCCTGTGTC	80227
rs756727736	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921118	CAGCCTGGCCAACAT[A/G]GCGAAACGCCATCTC	80227
rs756790463	snp	A/G	4.95536e-05	0.00497738	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916617	TTGCTATTGGCTGGG[A/G]CTCAAGATGGAAACA	80227
rs756801028	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73892645	TACATGCTATTTTAT[A/G]ACTTGCTTTTTGTTT	80227
rs756809991	snp	C/T	1.66178e-05	0.00288247	intron-variant	PAAF1	GRCh38.p7	11:73914519	GGCAAGTGGTTCCTA[C/T]ATGACCTTTGAACTC	80227
rs756864899	snp	A/G	1.64879e-05	0.00287118	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887392	CTGACTTGTCAAGGA[A/G]TTGGCCTAGATGGCA	80227
rs756965578	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73893660	GAGAATCGCTTGAAC[A/G]CGGGAGGCAGAGGTT	80227
rs756965775	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876746	TGAAGAACGCGGTAC[A/G]CGATGCTCACCGAAC	80227
rs757147116	snp	C/T	0.000297324	0.0121891	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900321	TGCAGGTTTTTCCCA[C/T]CAGGCCTTGTGGTCC	80227
rs757171095	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73903117	ATAACAGCCCTGACT[G/T]TTTTCTTGAGAAGGG	80227
rs757182121	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878246	AGCACCAGAATCAGA[A/C]GGCTTAATTTGCCCA	80227
rs757228655	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73902183	TTAAGTTTTAATATT[G/T]CTTTATAACATTTTG	80227
rs757230296	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73916207	GTGGGAATTGCAAGT[A/G]TTTCTCAGAAAGTTG	80227
rs757346123	in-del	-/GTAATCCCAGCACCTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAG	1.65488e-05	0.00287647	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924737	CTGGGTGATTCTCAT[lengthTooLong]GAGAGATCTAGGGCT	80227
rs757351591	in-del	-/T	0.000116071	0.00761721	intron-variant	PAAF1	GRCh38.p7	11:73909381	CTCCATCTTAGGGAG[-/T]TTTTTTTCTCTTGCT	80227
rs757409908	snp	C/G	0.000424133	0.0145563	utr-variant-5-prime, intron-variant, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73877043	GCGCCTTTGAGGATT[C/G]AGAGCGACTGGGCGC	80227
rs757496724	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73881319	TTAAACAGAATCTAG[C/G]TCTGTCACCTAGGCT	80227
rs757542707	snp	A/G	8.24804e-05	0.00642132	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918956	GAATCCTAGGGCTCC[A/G]GTACAAGTCATCCAC	80227
rs757562367	snp	C/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876794	CCGAACGCACGCTCC[C/T]ACGCGGCGGCTTGGG	80227
rs757572724	snp	C/G	1.66441e-05	0.00288474	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927363	CTTTCTGACCTCTGA[C/G]TTCTTGGAAAGAGCA	80227
rs757677431	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73885231	GCAACCTCTGCTTGC[C/T]AGGTTCAAGGTATTC	80227
rs757787147	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886782	TTGACCCCTCCAAAT[C/G]TCATGTTGAAATTTA	80227
rs758004302	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877778	ATAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	80227
rs758086151	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73917547	GTGGGCATCAGGCTT[G/T]GTTCAAGGCACTGAA	80227
rs758088665	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73895226	TGGGATGATTCAAAA[A/C]ATTTTGGCCTGAGAA	80227
rs758122159	snp	C/T	1.65141e-05	0.00287346	intron-variant	PAAF1	GRCh38.p7	11:73914363	GTGCTGTGTGGGCAC[C/T]ACCAGCTGATCAGCC	80227
rs758147099	snp	A/G	1.65814e-05	0.00287931	intron-variant	PAAF1	GRCh38.p7	11:73919077	CTTCTCTGTAGTTCA[A/G]TTAATTAAACATAGT	80227
rs758177157	snp	C/T	1.64977e-05	0.00287203	stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914490	CAGTGCTTGGGACTA[C/T]AGAGCAGGCAGCTGG	80227
rs758206562	snp	A/G/T	3.31643e-05	0.00407201	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899230	ATCTGGCAGGCTTCC[A/G/T]ATGGAGAACTCAGGG	80227
rs758207242	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73915474	GGGCATGGTGGCATG[A/C]ACCTGTAATCCCAGC	80227
rs758378368	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888048	CTACCATGCCCAAGC[A/G]AAATTGATTTTAATA	80227
rs758398601	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73882048	CTGGCTAATTTTGTA[-/T]TTTTTTTTTTTTAAT	80227
rs758415949	snp	A/G	4.99039e-05	0.00499495	synonymous-codon, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900299	ACATGTGTTTGATGT[A/G]AATTGTTGCAGGTTT	80227
rs758431806	snp	C/G/T	5.17088e-05	0.0050845	intron-variant	PAAF1	GRCh38.p7	11:73900452	CTCCAAAAGGCTTCT[C/G/T]TAATGATCCCCAGAA	80227
rs758460343	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876891	CACGGAAGGGGCGGG[C/G]AATGTGAAAAAGTCA	80227
rs758681804	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902003	CAAGTAGCTGGGATC[A/G]CAGGCGTGCACCACC	80227
rs758788058	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73894658	ATCTACTAAAAAAAA[-/T]AAAAATAAAAAAAAA	80227
rs758826692	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887130	CTCTTTTCTTTATAA[A/G]TTACCCAGCCTCAGG	80227
rs758841057	in-del	-/AAA			intron-variant	PAAF1	GRCh38.p7	11:73893749	TCTCCAAAAAAAAAA[-/AAA]AAAAAAAAAAGAAAG	80227
rs758893700	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908850	CTGGAGTGCAGTGGC[A/G]TGATCTCGGGTCACT	80227
rs758921153	snp	A/G	0.00233818	0.0341119	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889111	ACCATGCAAGCCTAC[A/G]TTTTTCCCAGGTGTT	80227
rs758942971	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73907562	GGTGGGCACCTCAGG[C/G]CACCTCTTTGTGCCT	80227
rs758983903	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73898654	AAACTCTGTCTCTAC[A/C]GAAAAATACAGAAAT	80227
rs758996947	snp	A/G	1.64866e-05	0.00287106	splice-donor-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924698	GACCCTGTGTACAAG[A/G]TACAGGCCTGAGACG	80227
rs759037665	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875938	CTGCCTCATTTGGTG[C/T]CCTTGGACACATCAT	80227
rs759133128	snp	A/G	1.68616e-05	0.00290353	missense, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900283	AGAGAGTATTGGAAG[A/G]ACATGTGTTTGATGT	80227
rs759157546	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73882772	CACGCCCAGCTAATT[G/T]TTTTGTATTTTTAGT	80227
rs759166346	snp	A/C/T	0.000148599	0.0086186	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927315	AAGCAGATCTACACA[A/C/T]GCTGTCGAGACGGTC	80227
rs759255577	snp	A/G	1.65211e-05	0.00287407	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900375	CTGAAGATATGGTCA[A/G]CTGAAGATGCTAGCT	80227
rs759305166	in-del	-/GCTGGCCTTGTGGCTGGCCTTGTGAATGGCCCCTGCACTCC	1.65985e-05	0.00288079	intron-variant	PAAF1	GRCh38.p7	11:73916663	GAGGAGTCCAAGGTG[lengthTooLong]AGTCACCATTCATTT	80227
rs759348601	snp	C/T	1.64789e-05	0.0028704	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909569	GACAACTCCATAAAC[C/T]TTGGCTCCCCTGAGC	80227
rs759361972	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73894080	AATGCTGGGATTATA[-/G]GTATAAGCCACTGTG	80227
rs759408328	snp	C/G			missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899182	AGCAGAGGAGGTCTT[C/G]GTGTGTCTTCTAGTA	80227
rs759455814	in-del	-/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888079	ATATATTTGATCTAA[-/C]CCAGTATATCTAAAA	80227
rs759456310	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73925841	CAATACAGAATGATA[C/T]AGATTTAAAAGTCTC	80227
rs759471442	snp	A/G	1.6486e-05	0.00287102	utr-variant-5-prime, splice-acceptor-variant, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878781	TCTTTCTTCGTAGGA[A/G]GGATGAAGGGGAGGC	80227
rs759518102	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73891533	GCAATCCTAGCACTT[C/T]GGGAGGCAGAGGCAG	80227
rs759576307	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73915964	AGAGGGAAATCAGGT[A/T]TTTTTGTTTGTTTAT	80227
rs759592281	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878530	TTTCAAAGTGAGCTC[A/G]CTGTTGATGGATGAG	80227
rs759597683	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73922063	ACTAATAGATGGCTT[A/C]ATCCACAGTATCTGT	80227
rs759626843	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73909802	AGCACTGCGTTTCAG[G/T]AAGTACAATCTAATG	80227
rs759660798	snp	C/T	1.68803e-05	0.00290515	intron-variant	PAAF1	GRCh38.p7	11:73916685	CATTCATTTACATGA[C/T]GCAGGTCTTCTGCAG	80227
rs759704225	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906932	TAAGCATCGTTAAAT[A/G]GGTTTTAATGAAACA	80227
rs759807427	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917156	CTCCTGAGTAGCTGG[A/G]ATTACAGGTGCGCGC	80227
rs759897489	in-del	-/CTAT	6.62153e-05	0.00575354	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878730	TGTAACTATGGGATC[-/CTAT]CTATTCAACTTTGGG	80227
rs759999168	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73927120	GATGCATCCATCACT[A/G]TGGGCCAACAATTTT	80227
rs760054035	snp	A/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914460	CTGCTCTTGGCCCGG[A/G]AAGATAAGAAACTTC	80227
rs760180623	snp	C/T	1.64958e-05	0.00287187	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916562	GTTCCTCTTTATTGG[C/T]TCAGACGCTTTCAAC	80227
rs760235963	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73922548	ATAGGCCGGGCACAG[G/T]GGCTCACACCTGTAA	80227
rs760253215	snp	G/T	1.64841e-05	0.00287085	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919023	AGAGATGGATTCATT[G/T]CTAGCCAAGGTGGGT	80227
rs760277562	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73918233	AGAAGTGATACCAGC[A/G]GGAAAACAGGAGCTG	80227
rs760315567	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879774	GCTACTTGGGAGGCT[A/G]CAATAGGAGGATCTC	80227
rs760328910	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921026	CATCTCTGGCTGGGT[A/G]CAGTGGCTCACATCT	80227
rs760377649	snp	C/T	0.000230624	0.0107359	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924655	GCAAGACTTAGACTA[C/T]GTCACTGAGCTCACT	80227
rs760418371	snp	C/T	1.64806e-05	0.00287054	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909414	GTATCCTGGATACAG[C/T]CATCGTTGATCGGGG	80227
rs760419018	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921037	GGGTGCAGTGGCTCA[C/T]ATCTGTTATCCCAGC	80227
rs760489021	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899744	AGAACCTTTCTCAAG[C/T]TCAGTGATTTGGCAG	80227
rs760558984	in-del	-/AAACTT			intron-variant	PAAF1	GRCh38.p7	11:73894616	TGCACGTGTACCCTA[-/AAACTT]AAAGTATAATAATAA	80227
rs760636407	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73901621	TTTTTTTTTTTTTTT[-/A]AGATGGAGTCTCACT	80227
rs760678177	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918791	AATTACCTTAATCTG[C/T]CAGTTAAGGTTCTTG	80227
rs760752064	snp	A/C	1.65718e-05	0.00287848	intron-variant	PAAF1	GRCh38.p7	11:73916540	TGCCTCCTACTTGTT[A/C]CCAGGTGTTCCTCTT	80227
rs760791288	in-del	-/AC			intron-variant	PAAF1	GRCh38.p7	11:73880309	AATATATATATATAC[-/AC]ACACACACATATACA	80227
rs760835804	snp	A/G	0.000105871	0.00727489	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887306	TTCAAAGAGAAAAAT[A/G]ATAAATTTTTCTTAT	80227
rs760874962	snp	A/G/T	3.35357e-05	0.00409472	splice-donor-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887458	AATGAAATAAACAAG[A/G/T]TATGTTTTTATGTCT	80227
rs760919158	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73890243	TGCAAGAGTCCTTGA[A/G]GGAGGGTTTACCAAG	80227
rs760993620	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908417	ATATATATGTGTGTA[-/TA]TATATATATATGGGT	80227
rs761047430	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73905230	GAAATTGCTGCTTTC[-/T]TTTTTTTTTTTGAGA	80227
rs761131280	snp	C/G			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927297	TAGGTAGCCACATGG[C/G]AGAAGCAGATCTACA	80227
rs761236205	in-del	-/T	3.3461e-05	0.00409016	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887339	TTTGAGACATGCTTC[-/T]TTTGTACCATATAGG	80227
rs761236941	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914220	TATTTTTAATTGTAT[A/G]GTTCTGTGAGTTTTG	80227
rs761257322	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73910410	TAGGTGTAGGGGCAG[C/T]TTGCATTATAGCTTG	80227
rs761376744	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909468	GAGATGGGACAGCAC[A/G]ACTTTGGGATTGTGG	80227
rs761403107	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894009	AGTCCTGCTCTGTTG[C/T]CCAGGCTGGTCTCAA	80227
rs761453777	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894965	TTCCAGGCTGGGTGA[C/T]AGAGTGAGACCATGT	80227
rs761571953	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73908787	TACTTAATTTTTATT[A/T]TTTATTTATTTATTT	80227
rs761582240	snp	C/T	1.72531e-05	0.00293705	intron-variant	PAAF1	GRCh38.p7	11:73918902	GAATATAGTCAAGTA[C/T]TGCTTTTGAAGAAAG	80227
rs761722548	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917442	TCACACAATCTCTCT[A/G]TTGCAGGATTTAACA	80227
rs761734273	snp	A/G	3.30306e-05	0.00406377	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927324	TACACATGCTGTCGA[A/G]ACGGTCTTGTACGAC	80227
rs761784691	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73880111	CTGTAGTCCCAGCTA[C/T]TCAAGAGGCAGAGGT	80227
rs761820784	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890470	TGGGGCATCAAAATA[C/T]AGCTGTGTTACAACA	80227
rs761845668	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908374	GTGTATATATATATG[-/TA]TATATATGTGTGTAT	80227
rs761961976	snp	C/G	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909577	CATAAACCTTGGCTC[C/G]CCTGAGCAGATGCCC	80227
rs761975004	in-del	-/CTTA			intron-variant	PAAF1	GRCh38.p7	11:73886124	TGTGTAGGATAGTAT[-/CTTA]CTTAGCCCATATCTC	80227
rs761994780	snp	A/C			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875911	GAAACAGACTTGGAC[A/C]TAGCTTTGTCACTGC	80227
rs762054737	snp	G/T	3.29592e-05	0.00405938	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919000	CAGTTCTATCCCTGC[G/T]AAGTGTCAGAGATGG	80227
rs762086926	snp	C/G	1.64803e-05	0.00287052	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878794	GAAGGATGAAGGGGA[C/G]GCCTGGCTGAGCTGT	80227
rs762088850	snp	G/T	1.648e-05	0.0028705	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914424	GCAGGTGAACGGGAG[G/T]TTGGAACAGAGGCCA	80227
rs762175614	snp	A/G	6.61255e-05	0.00574964	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899170	CTGGACATTTCCAGC[A/G]GAGGAGGTCTTGGTG	80227
rs762200333	snp	C/T	0.00016481	0.00907622	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914418	TGTCATGCAGGTGAA[C/T]GGGAGGTTGGAACAG	80227
rs762306968	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73911454	TCCCAAAGTGCTAGG[A/G]TTACAAGCATGAGCC	80227
rs762334840	snp	C/T	1.65787e-05	0.00287907	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900392	TGAAGATGCTAGCTG[C/T]GTGGTGACCTTCAAA	80227
rs762357223	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73925431	TGATTGTACCATTGC[A/C]CTCTAGTCTGGGCAA	80227
rs762371943	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73914053	ACAACATACTAGACT[C/G]TGTCTCAAAAAAAAG	80227
rs762378132	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73902719	TTATTTTTTTTGAGA[A/T]GGAGTCTCACTCTGT	80227
rs762409885	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73926998	CTCCTCCCTAGAGGC[A/C]GACCATCTGTGCTAA	80227
rs762412303	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73896099	GAGCAACAGAGTGAG[A/T]CCCTGTCTTTAAAAA	80227
rs762431495	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73901771	GATGGGGTTTCACCA[C/T]ATTGGTCAGGCTGGT	80227
rs762473752	in-del	-/TTAA	0.000145106	0.00851658	intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889018	ACCAACTCAGAGAGG[-/TTAA]TTAATCTCAAATAAT	80227
rs762538485	in-del	-/C	3.29788e-05	0.00406058	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916620	CTATTGGCTGGGACT[-/C]AAGATGGAAACATTT	80227
rs762602932	in-del	-/AT			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875660	GATAGAATCTGACAC[-/AT]GAGAGCAAAAAAAAA	80227
rs762653408	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73921758	CGAAAACTTTCTCAC[A/C]AAGTCTCAGCCCAGT	80227
rs762678409	in-del	-/AAG			intron-variant	PAAF1	GRCh38.p7	11:73910307	GGAAAGATGTCACAA[-/AAG]AAGTTGGCTTGAACC	80227
rs762713515	snp	C/G	0.000608828	0.0174368	missense, intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887066	CATCAGAAGCAGATG[C/G]TGGTGCCATGCTTCT	80227
rs762873945	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73883075	GGCTAATTTTTTAAA[-/T]TTTTTTGTAGAGACA	80227
rs762884602	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73893195	GAATACATTTGTAAA[A/G]GTGGAATTGCTAAGT	80227
rs762941466	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73905338	AAGTGATTCTTCTGC[C/G]TCAGCTTCCCAAGTA	80227
rs762996482	snp	C/G			stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918976	AAGTCATCCACAGAT[C/G]AGGAGCACCAGTTCT	80227
rs763116446	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877331	AGAAAGACAGGGATA[C/G]TGGGAGGCAGGAAGG	80227
rs763123240	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73904597	TCTTAGAAATTGGCT[A/G]TGCCGCCTCCAAGTA	80227
rs763126253	snp	C/T	0.000466994	0.0152735	intron-variant	PAAF1	GRCh38.p7	11:73914525	TGGTTCCTATATGAC[C/T]TTTGAACTCTGAGGC	80227
rs763344174	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73902759	TGGGGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	80227
rs763363623	snp	A/G	1.64814e-05	0.00287061	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914419	GTCATGCAGGTGAAC[A/G]GGAGGTTGGAACAGA	80227
rs763436282	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73925877	CGACCTTTTTGGTTC[C/T]CTTTCTCTTTTCCAG	80227
rs763451040	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73889772	TGGTACAAGAGGCAG[A/T]TCCAAATCCAGGCCA	80227
rs763506149	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891678	TACTCAGGAGGCTGA[A/G]GTGGGAGAATTTTTT	80227
rs763511268	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921067	CACTTTGGGAGGTCA[A/G]GGCGGGTGGATCAGC	80227
rs763596964	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918391	TTTTTTTTGCCTCCA[C/T]AGAGATAGGGAATCT	80227
rs763617103	snp	A/G	8.3111e-05	0.00644582	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900398	TGCTAGCTGCGTGGT[A/G]ACCTTCAAAGGTCAC	80227
rs763618203	snp	A/C	1.80396e-05	0.00300325	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891166	TCTAAGTTTTTGGCA[A/C]CATATACTACTTTTT	80227
rs763662175	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73883343	CATATATTATTTCTA[A/G]TATCACCCCCAAAAC	80227
rs763785437	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73907380	GCACTGACTCATACC[A/G]CCTCACACTGCAGAC	80227
rs763791020	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921408	CTTTTTTTTTTTGGA[A/G]TGTTAGAAATTTCTT	80227
rs763977788	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908695	TGTACCACTGCACCT[A/G]GCCAAGGCAGTGATT	80227
rs764011120	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73901652	CTGTCGCCTAGGCCG[G/T]AGTCCAGTGGCATGA	80227
rs764011133	in-del	-/GC			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876681	ACTTTGAGGACGCAT[-/GC]GCGCGCGCGCGGCCG	80227
rs764051708	snp	C/T	1.66156e-05	0.00288228	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924746	TTCTCATGAGAGATC[C/T]AGGGCTTTTATGAGA	80227
rs764094069	in-del	-/TA	1.6475e-05	0.00287006	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924647	TTGTCCAGCAAGACT[-/TA]TAGACTATGTCACTG	80227
rs764104830	snp	C/T	1.65132e-05	0.00287339	stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927321	ATCTACACATGCTGT[C/T]GAGACGGTCTTGTAC	80227
rs764136930	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73905309	GCTCAGTGCAACCTC[C/T]GCCTCCTGGGTTCAA	80227
rs764186304	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904331	AGTTAAATTGCCCAG[G/T]CCATTTAAGTAAGCT	80227
rs764475421	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875582	CTGAAACTTGACAGA[C/T]GGAACAGAAGTTAGC	80227
rs764517957	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73913038	TGCACTACCATGCCT[C/G]GCTATTTTTTGTATT	80227
rs764520402	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73907333	TTCAGCCACCTACTG[G/T]ACTCCCCTGACACTA	80227
rs764520434	snp	A/C	1.74139e-05	0.0029507	intron-variant	PAAF1	GRCh38.p7	11:73916707	CTTCTGCAGAGTGGA[A/C]ATTTTTATTGGCTTT	80227
rs764554707	snp	C/T	0.000136977	0.00827464	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889114	ATGCAAGCCTACGTT[C/T]TTCCCAGGTGTTTTG	80227
rs764579112	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73912108	TGCTACTTCTTAAAG[G/T]TCTCCTTTTATGAAA	80227
rs764631532	in-del	-/T	5.13044e-05	0.00506454	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887479	TTTATGTCTTCTAGA[-/T]TGGCATGATATTTAA	80227
rs764694549	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73925609	TAAATATTATTCATT[A/C]TTATTATTATTAAGA	80227
rs764752327	snp	C/T	1.65029e-05	0.00287248	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924712	GGTACAGGCCTGAGA[C/T]GACACCAGACCTGGG	80227
rs764755187	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73910865	TGTGGTAGTGTGTGC[A/C]TGTAATCCCAGCTAC	80227
rs764779247	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921960	GAGTTCCTTCAGACA[C/T]TCAGAAACGTAGACA	80227
rs764788014	snp	C/T	1.65466e-05	0.00287628	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900385	GGTCAGCTGAAGATG[C/T]TAGCTGCGTGGTGAC	80227
rs764813069	snp	C/T	1.67897e-05	0.00289733	synonymous-codon, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900287	AGTATTGGAAGGACA[C/T]GTGTTTGATGTGAAT	80227
rs764855704	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893680	AGGCAGAGGTTGCAG[C/T]GAGCCAAGATTGCGC	80227
rs764921049	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73904263	AAAGTAGTTTTGTGA[C/T]TGTAACATATGAGTT	80227
rs764951703	snp	G/T	1.64846e-05	0.0028709	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878783	TTTCTTCGTAGGAAG[G/T]ATGAAGGGGAGGCCT	80227
rs764967143	snp	G/T	3.29587e-05	0.00405934	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909570	ACAACTCCATAAACC[G/T]TGGCTCCCCTGAGCA	80227
rs764997700	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909881	CTTCCCTGGGCCACA[C/T]TGGAAGACTTGTCTT	80227
rs765023720	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73917466	TTTAACAATTTCTAC[A/G]ATTTTGTCCCTTCCT	80227
rs765046962	in-del	-/ATAA			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878491	TTTACAATAATCCTG[-/ATAA]ATAATTAAATAACCT	80227
rs765081577	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73895163	GATGTGGGACTAGAC[A/G]TGATTTGCTGATGAC	80227
rs765154444	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73919200	GTGATTGTCTGTGTC[A/C]CCCTCCAGTTCAAAC	80227
rs765282590	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73891465	GGAGAGTTACCAGCT[C/T]TCAGATAATGATATA	80227
rs765303228	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73890550	CACCGTAAGCCTGAC[C/G]CAGGCCTACATATTT	80227
rs765343890	in-del	-/G			intron-variant	PAAF1	GRCh38.p7	11:73926240	CCTCTCGAGCAGCTG[-/G]GGATTACAGGCATGC	80227
rs765390402	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906691	GTGGCATTTTCTTAA[A/G]CTCATCTTTTTCTAA	80227
rs765495666	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73913160	GGGATTACAGGCGTG[A/G]GCCACCGCACCTGGC	80227
rs765672458	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73901973	GGCTCATGCGATCCT[C/T]GTGCCTCAGCTTCTC	80227
rs765766048	snp	A/C	1.64806e-05	0.00287054	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914462	GCTCTTGGCCCGGGA[A/C]GATAAGAAACTTCAG	80227
rs765819607	snp	C/T	1.64936e-05	0.00287168	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916564	TCCTCTTTATTGGCT[C/T]AGACGCTTTCAACTG	80227
rs765826928	snp	C/T	1.68485e-05	0.00290241	intron-variant	PAAF1	GRCh38.p7	11:73918927	AGAAAGAAAGTAAAA[C/T]TTCCCCTTTCTCTGA	80227
rs765828556	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73927019	TCTGTGCTAAACCTG[A/C]ACAATACTAATGGGT	80227
rs765836335	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73885567	CCCTCCCGGCCTGGT[C/T]GTGGTGGCTCACACC	80227
rs765867314	in-del	-/TTTG	6.59587e-05	0.00574239	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916622	TTGGCTGGGACTCAA[-/TTTG]GATGGAAACATTTAT	80227
rs765897267	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73910253	ATGCAAATATAATAG[A/G]TTTTCAGAGGGACGG	80227
rs765906550	snp	C/T			intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889193	ATACAGTCTTTATCA[C/T]TTCAAACATGATTGC	80227
rs765939931	snp	G/T	1.6492e-05	0.00287154	intron-variant	PAAF1	GRCh38.p7	11:73919035	ATTGCTAGCCAAGGT[G/T]GGTCCATGGGCCAAT	80227
rs765958612	in-del	-/TT			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875788	TAGGGAGTTTAAGAC[-/TT]TTTATTCTGAGGGCA	80227
rs765993343	snp	A/G	1.651e-05	0.0028731	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899194	CTTGGTGTGTCTTCT[A/G]GTACTGACGGGACCA	80227
rs766057388	snp	C/T	4.94499e-05	0.00497217	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919019	TGTCAGAGATGGATT[C/T]ATTGCTAGCCAAGGT	80227
rs766205654	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880612	GAATGGAGTGAACCC[A/G]GGAGGCGGGGCTTGC	80227
rs766217915	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917637	AGCACTTTGGAAGGT[C/T]AAGGTGGGTGGATCA	80227
rs766284232	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73905515	GCATGAGCTACCATG[C/T]CTAGCCAAAATTGCT	80227
rs766304197	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73910989	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	80227
rs766374567	snp	A/G	2.41706e-05	0.00347631	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887311	AGAGAAAAATAATAA[A/G]TTTTTCTTATTTTTT	80227
rs766408128	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73925715	TGAACGTTTTATATA[C/T]GTTATCTCATGTAAT	80227
rs766456196	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73915844	TTTCATCTTGTTACT[C/G]CACTGTGCTGGTGAT	80227
rs766485805	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73893294	TCAATTGTTGCTCTT[A/C]ATTTCCTCTGTAAAA	80227
rs766610506	snp	A/G	1.69089e-05	0.0029076	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887468	ACAAGGTATGTTTTT[A/G]TGTCTTCTAGATGGC	80227
rs766650093	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73906598	TTGAAAAGTTACACT[A/G]TAGTGATTAGGTCCC	80227
rs766685731	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73902786	ACTGCAACCTCTGCC[G/T]CCTTGGTTCAAGCAA	80227
rs766691155	snp	A/G	1.70909e-05	0.00292321	synonymous-codon, intron-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900272	TTTGTTTTTCCAGAG[A/G]GTATTGGAAGGACAT	80227
rs766832548	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887242	CCTGTTTTTCTTTCG[C/T]GGGCCAATTTCATGG	80227
rs766886382	snp	C/T	1.65891e-05	0.00287998	intron-variant	PAAF1	GRCh38.p7	11:73909611	AAGTTGATAATGATA[C/T]GTAGCATTGTTTTAT	80227
rs766956442	in-del	-/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877634	TCATGCCTGTAATCC[-/T]CAGCACTTTGGAAAA	80227
rs766972498	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912827	CATTTCAGCCACAGG[C/T]CTTCAGTTTCTTCTT	80227
rs766995484	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899715	CCGCTCCTGGCCTCT[C/T]AGCTGTCAATTCGAG	80227
rs767132712	snp	A/G	1.71876e-05	0.00293147	intron-variant	PAAF1	GRCh38.p7	11:73918913	AGTATTGCTTTTGAA[A/G]AAAGAAAGTAAAATT	80227
rs767148734	in-del	-/AAAC			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874992	CTCCATCTCCAAAAC[-/AAAC]AAACAAACAAACAAA	80227
rs767226509	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73882827	GCAGGATGGTCTCGA[A/T]CTCCTGACCTTGAGA	80227
rs767401064	in-del	-/T	1.65214e-05	0.0028741	intron-variant	PAAF1	GRCh38.p7	11:73924600	GTTATATGAATTTTC[-/T]TTTCTGCCTTTCAGG	80227
rs767412356	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73891555	CAGAGGCAGGAGGAT[C/T]ACTTGAGGCCAAGAG	80227
rs767416690	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73894518	GATAGCATTAGGAGA[-/T]GTACCTAATGTTAAA	80227
rs767423239	snp	A/G	1.67638e-05	0.0028951	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900418	TCAAAGGTCACAAAG[A/G]AGGTATGAAGTGTGC	80227
rs767427605	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73896899	GCGCCCCTCACCTCC[C/T]GGACGGGGCGGCTGG	80227
rs767488920	in-del	-/TTGT	0.000140142	0.00836967	intron-variant	PAAF1	GRCh38.p7	11:73899123	ATTATTTCTAACACA[-/TTGT]TTGTTTTCTCTTTGA	80227
rs767533355	snp	C/T	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909514	GGGAGTCCTTGCAGA[C/T]TGTGGTTCTTCTATC	80227
rs767548143	snp	C/T	1.64974e-05	0.00287201	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909400	TTTTCTCTTGCTAGG[C/T]ATCCTGGATACAGCC	80227
rs767557700	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917169	GGGATTACAGGTGCG[C/T]GCTACCACACCCAGC	80227
rs767600114	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73880688	CAAGACTCTGTCTCG[-/A]AAAAAAAAAAAAAAA	80227
rs767608993	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73915965	GAGGGAAATCAGGTT[A/T]TTTTGTTTGTTTATT	80227
rs767668175	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886455	CTGAGGCGAGTGGAT[C/T]ACGAGGTCAGGAGAT	80227
rs767692374	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73904208	AAGCAGAGGTAAGGT[C/T]TCTGTGTATGCTGAA	80227
rs767713021	snp	C/T	3.29609e-05	0.00405948	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878796	AGGATGAAGGGGAGG[C/T]CTGGCTGAGCTGTCA	80227
rs767717524	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878588	CATTAAATAGTTAAT[C/T]CACAAATATTTCTTG	80227
rs767733173	snp	C/G	2.05941e-05	0.00320884	intron-variant	PAAF1	GRCh38.p7	11:73891213	GAGTGTAAGTATTTT[C/G]ATAAAATGAAGAGAA	80227
rs767766345	snp	C/T	0.000363736	0.0134809	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887114	CGTGAGCCAAATAAA[C/T]CTCTTTTCTTTATAA	80227
rs767779913	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888736	TTTTCATAAACAGCT[A/G]TGGGTATTATAGGTA	80227
rs767829334	snp	A/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73919012	TGCTAAGTGTCAGAG[A/G]TGGATTCATTGCTAG	80227
rs767872309	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73890222	TAGAGTAAGGGACTG[G/T]CATATTGCAAGAGTC	80227
rs768013157	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912011	TGGTATTTCACATAG[C/T]AAACCCTCTCCTCAA	80227
rs768062742	snp	C/T	3.3054e-05	0.00406521	intron-variant	PAAF1	GRCh38.p7	11:73909391	AGGGAGTTTTTTTCT[C/T]TTGCTAGGTATCCTG	80227
rs768139675	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73904768	TGTTAAGAATATACA[A/C]CTGGGAATATGAAAT	80227
rs768177356	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888209	CAGCTTATCTCAGCT[C/T]AGACTCTAATTTTTA	80227
rs768231462	snp	A/G			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916584	GCTTTCAACTGCTGT[A/G]CTTTTCTCTCTGGCT	80227
rs768284578	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73915538	ACCTTAGCCTGGAAG[G/T]TCGAGGCTGCAGTGA	80227
rs768348407	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909457	GTCTGCTTCTCGAGA[C/T]GGGACAGCACGACTT	80227
rs768391310	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886831	AGGGCCTAATGGGGG[G/T]TGTTTGGGTCATGGG	80227
rs768497391	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73893015	CTATGCTGTCTTTCA[A/T]TGTATCCTTCTAAGA	80227
rs768578603	snp	C/T	4e-05	0.00447196	intron-variant	PAAF1	GRCh38.p7	11:73891100	GAATCTCATCTTTTC[C/T]TCTTTGTTTAGAAAA	80227
rs768579544	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73903632	TGAGGCAGGAGAATC[A/G]CTTGAACTCAGGAGG	80227
rs768702105	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73911552	CCATTTACTCTTCAA[C/T]CCATTCTAGGATGGT	80227
rs768704732	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73891102	TCTCATCTTTTCCTC[-/T]TTTGTTTAGAAAAGC	80227
rs768821351	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73883843	TTTTTATCAGTACTT[C/T]GTTCCTTTTTGTGGC	80227
rs768878564	snp	A/G	3.71402e-05	0.00430914	intron-variant	PAAF1	GRCh38.p7	11:73899289	TAAACACAAAGGGTG[A/G]TCTGAGAAGCCTTGG	80227
rs768931532	snp	A/T	1.65422e-05	0.0028759	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878742	GATCCTATTCAACTT[A/T]GGGTAAGCCTAATTA	80227
rs768966931	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73892909	TTGTGATCCGCCCAC[C/G]TCGGCCTCCCAGAGT	80227
rs768989946	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921862	GCATTAAGTGGAAAA[C/T]CAGGTTCTCCAGGAA	80227
rs769018291	snp	A/G	0.000113912	0.00754606	intron-variant	PAAF1	GRCh38.p7	11:73891234	ATGAAGAGAAAATGT[A/G]ATAGCATGTTAATTT	80227
rs769020355	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73907742	CCCACTGAAACCATG[C/G]GGGAGGGGAAGTAAC	80227
rs769032408	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73901165	AGGGAACAGTAAAAG[C/G]TGGGTGGCTAATGGC	80227
rs769033401	snp	A/G	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918992	AGGAGCACCAGTTCT[A/G]TCCCTGCTAAGTGTC	80227
rs769087936	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877127	ATGTTGCTTTGCGTC[A/G]AGGAGAGCCATGCCT	80227
rs769114570	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887334	TATTTTTTGAGACAT[A/G]CTTCTTTTGTACCAT	80227
rs769196752	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877848	CCGAGATTGCACCAC[G/T]GCACTCCAGCCTGGG	80227
rs769239456	in-del	-/G	3.48864e-05	0.00417636	intron-variant	PAAF1	GRCh38.p7	11:73916495	TGCCTGTTTATTCTT[-/G]GAAACAAATTAATCT	80227
rs769324245	snp	A/G	1.66657e-05	0.00288662	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899148	TCTCTTTGAACAGAT[A/G]ACATGCCTGGACATT	80227
rs769379689	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73904815	AAATATTTATTTCAG[G/T]AATAGTTTCATCTAA	80227
rs769420768	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73901606	GATCAAGTTTTAAGA[-/T]TTTTTTTTTTTTTTA	80227
rs769434753	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73903483	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAT	80227
rs769481022	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73911732	CCAGGTTCAAGTGTT[A/C]GAGTGATTCTTGTGC	80227
rs769494625	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73926889	TCCTTGAGGAGTTGA[C/T]GAAATCCTCCTCAGA	80227
rs769521752	snp	A/C	3.35435e-05	0.0040952	intron-variant	PAAF1	GRCh38.p7	11:73909359	CCTTGTAGTTCCTTT[A/C]CTCCATCCTCCATCT	80227
rs769607993	snp	C/G			downstream-variant-500B	PAAF1	GRCh38.p7	11:73928155	AATCAGAAATTCTAC[C/G]GGTGCAGCCAGCAGT	80227
rs769609726	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73912525	TCCCTCTCCCTCCCC[C/G]TCTCTCCCTTCCTCC	80227
rs769615074	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73889745	AGAGGATTTAGCTGA[C/T]GCTTTAGTTTCTGGT	80227
rs769718630	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73882846	CTGACCTTGAGATCC[A/G]CCCACCTCGGCCTCC	80227
rs769739929	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73908114	AGGAGCAATGGGACT[A/G]CTCTTTCTTGGCCAA	80227
rs769839312	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899500	CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGCG	80227
rs769957647	snp	C/G	5.16622e-05	0.00508217	intron-variant	PAAF1	GRCh38.p7	11:73916700	TGCAGGTCTTCTGCA[C/G]AGTGGAAATTTTTAT	80227
rs769967577	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73920082	AGTAGTGTACCAATA[C/T]TGGCATCTTAGTTTT	80227
rs770010550	snp	C/T	1.79021e-05	0.00299177	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891150	AAAGGAAAATGCATC[C/T]TCTAAGTTTTTGGCA	80227
rs770012471	snp	C/T	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918971	GGTACAAGTCATCCA[C/T]AGATCAGGAGCACCA	80227
rs770026834	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921991	GAGATACGTATATCA[A/G]GGTCCTGTCAGCTTC	80227
rs770027256	in-del	-/TTTCTTTT			intron-variant	PAAF1	GRCh38.p7	11:73896276	TTTTTTTTTACGATG[-/TTTCTTTT]TTTCTTTTTTTCTTT	80227
rs770028332	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73918153	CCCATATATGAAGGC[A/T]TGTGAAGGGGATTGT	80227
rs770051699	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73903022	AAATCAATTTAGATA[C/T]AAGCTTTTATTCATG	80227
rs770105940	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878173	GCTAGTACACAGAAT[A/G]TGATAAGTAATAAAG	80227
rs770121634	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909115	TTTTAAAAAAGAGTT[C/T]TGAAGACAAAATAAA	80227
rs770159471	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877288	GAGCTGTGTGATCCC[C/G]GCGTCAGAACTAGTA	80227
rs770260876	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73915639	GCATTCAGGACTCTT[C/G]ATCAATTAATGAACA	80227
rs770374247	snp	C/T	1.65002e-05	0.00287225	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878849	TTATATATGCTGTGA[C/T]TTTAAAGGAGAAGGA	80227
rs770547570	snp	C/G	9.88517e-05	0.00702966	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924664	AGACTATGTCACTGA[C/G]CTCACTGGGGCTGAC	80227
rs770562837	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73901362	AGGTATGTTTTATCC[A/T]TAATTGGAGTATTAA	80227
rs770629537	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73912657	AGAAAATCATAAGTC[A/T]TGTCACATTCCTGCT	80227
rs770717402	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73899654	TCACGTCAAGTGATC[C/T]GCCCACCTTGGCCTC	80227
rs770731678	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912964	TCACTGCAACCTCCA[C/T]CTCCTAGGTTCAAGC	80227
rs770737633	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73886047	TATAGACATGAATAT[A/T]TAAGGTGTAGAAGAA	80227
rs770757520	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875225	AGCATACAGAAGGAA[C/T]TTAAGGTTTGAAGAG	80227
rs770786625	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73888036	TACAGGCGTGAGCTA[A/C]CATGCCCAAGCGAAA	80227
rs770818038	snp	C/G	1.65053e-05	0.0028727	intron-variant	PAAF1	GRCh38.p7	11:73914380	CCAGCTGATCAGCCT[C/G]ACTGTTATTAACATA	80227
rs770869078	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73894451	TCAAGACCAGCCTGG[C/T]CAACATAATGAAACC	80227
rs770891888	snp	C/G	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909562	TGCTGCTGACAACTC[C/G]ATAAACCTTGGCTCC	80227
rs771035871	snp	A/G	4.94752e-05	0.00497344	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878775	CTTTTGTCTTTCTTC[A/G]TAGGAAGGATGAAGG	80227
rs771037297	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73895130	ATAAAACTGCCCTTA[A/T]AGATCTTACATGCTA	80227
rs771049374	snp	C/T	1.65551e-05	0.00287702	intron-variant	PAAF1	GRCh38.p7	11:73916542	CCTCCTACTTGTTCC[C/T]AGGTGTTCCTCTTTA	80227
rs771082710	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73911268	GCCCTAATAATCCTC[G/T]GTACTCTGTTCAAGC	80227
rs771099914	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878423	AAGGAATCTTGTTTG[G/T]TTATTGTGAGGGTTA	80227
rs771170251	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879776	TACTTGGGAGGCTGC[A/G]ATAGGAGGATCTCTT	80227
rs771179997	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918139	CCCATGTATAGAATC[C/T]CATATATGAAGGCAT	80227
rs771223177	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73895778	TTTGTTATTCTGATA[A/G]TGGCTTATGCATGAA	80227
rs771234830	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73920614	TCCCAGCACTTTGGG[-/A]AGCTGAAGCGGGTGG	80227
rs771237926	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874839	AAAAATACAAAAATT[A/G]GGCGGGCGTGATGGC	80227
rs771242610	snp	A/G	8.25498e-05	0.00642402	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927312	GAGAAGCAGATCTAC[A/G]CATGCTGTCGAGACG	80227
rs771309025	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73903805	TTAAAAAAAATTGGC[C/T]GGGCGCAGCGTCTCA	80227
rs771361961	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73916902	GAAAATTAAGCTTAA[A/T]TATAAACTAACATTT	80227
rs771410805	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73904952	GTATCTATTTGGTTT[A/G]ATATCTAAAGCCTTT	80227
rs771669139	snp	C/T	3.29468e-05	0.00405861	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909485	CTTTGGGATTGTGGG[C/T]GCTCAGCCTGCTTGG	80227
rs771722549	snp	G/T	0.000879576	0.0209527	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909547	TGGAGTGGCGGTGGG[G/T]GCTGCTGACAACTCC	80227
rs771776176	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73901591	TAACTTGTGTGTGGA[C/G]ATCAAGTTTTAAGAT	80227
rs771812793	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73886359	TCTCTAAATCTTTGT[C/T]CTTAGCTTTTAGTCT	80227
rs771846952	snp	C/T	1.65064e-05	0.00287279	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878763	AGCCTAATTAGGCTT[C/T]TGTCTTTCTTCGTAG	80227
rs771866167	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73884143	GGTAAGTGGTTGGAT[G/T]GATCCTAGTTCTGCT	80227
rs771904194	snp	C/T	1.64814e-05	0.00287061	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878817	TGAGCTGTCATCCCC[C/T]AGGTAATACCCATGA	80227
rs771957222	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908375	GTATATATATATGTA[-/TA]TATATATGTGTGTAT	80227
rs772334166	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73918581	TCCCGGGTTCCCGCC[A/G]TTCTCCTGCCTCAGC	80227
rs772419613	in-del	-/G	6.70556e-05	0.00578993	intron-variant	PAAF1	GRCh38.p7	11:73909634	TGTTTTATTTTCTTA[-/G]GCCCCCTTCAGTGAT	80227
rs772427683	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73920022	TTGGATCCAGGATGT[A/T]AAGGAAAGACTGGTG	80227
rs772439889	snp	C/T	1.64754e-05	0.00287009	stop-gained, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924641	TGTTTTATTGTCCAG[C/T]AAGACTTAGACTATG	80227
rs772444313	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875411	TAAGTCAGTTAAGTT[C/T]CTGGCTTCATGGAGT	80227
rs772446378	snp	C/T	1.76331e-05	0.00296922	intron-variant	PAAF1	GRCh38.p7	11:73900240	GGATGGACAAGAGAA[C/T]TAGCATGGAATTTTC	80227
rs772467657	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73881531	GAGCTCAAGTGATCC[G/T]CCCGCCTTGGCCTCC	80227
rs772509129	in-del	-/C	6.59598e-05	0.00574243	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878835	TAATACCCATGAATT[-/C]ATATATGCTGTGACT	80227
rs772531653	in-del	-/TC	1.64817e-05	0.00287064	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916589	CAACTGCTGTACTTT[-/TC]TCTCTGGCTTCTTGC	80227
rs772553884	snp	A/C	1.65214e-05	0.0028741	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927292	TGTTTTAGGTAGCCA[A/C]ATGGGAGAAGCAGAT	80227
rs772614790	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73892736	GCAGTCTCGGCTCAC[C/T]GCAAGCTCCACCTCC	80227
rs772674202	snp	A/G	1.6507e-05	0.00287284	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900345	GTGGTCCTGAGTGGG[A/G]GAATGGATGCCCAGC	80227
rs772713018	snp	C/T	6.59011e-05	0.00573988	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909553	GGCGGTGGGTGCTGC[C/T]GACAACTCCATAAAC	80227
rs772721109	snp	A/G			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925057	TTACTTGGGAGGCTG[A/G]GGCAGGAGAATCGCT	80227
rs772738121	snp	A/G			downstream-variant-500B	PAAF1	GRCh38.p7	11:73927833	GCCTGGCCATAGAGA[A/G]GGCCTGCTTGGCAGT	80227
rs772802804	in-del	-/A	3.45173e-05	0.00415421	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887492	GATGGCATGATATTT[-/A]AAAACTATGGTAGTA	80227
rs772841186	in-del	-/GTTTT			intron-variant	PAAF1	GRCh38.p7	11:73923496	TTGTTTAGTTTTAAA[-/GTTTT]GTTCAGTGAGCATGT	80227
rs772864689	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73926902	GATGAAATCCTCCTC[A/G]GAAAAAAAGACACAT	80227
rs772865385	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908416	GTATATATATGTGTG[-/TA]TATATATATATGGGT	80227
rs772910995	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888450	ATGGGTAAGCAAAGC[A/G]TTGGAGAACCCATGA	80227
rs772924880	snp	A/C			intron-variant	PAAF1	GRCh38.p7	11:73906360	CGGGTTCAAGTGATT[A/C]TTGTGCCTCAGCCTC	80227
rs772972908	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73918855	CTTCACATTTTATCC[C/T]GTTTGCTCTTATGTG	80227
rs773031210	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912536	CCCCCTCTCTCCCTT[C/T]CTCCTGTCAACATCT	80227
rs773321203	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908327	ATATGTGTATATATG[-/TA]TATATATATGTGTAT	80227
rs773358854	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877291	CTGTGTGATCCCCGC[A/G]TCAGAACTAGTATCA	80227
rs773382573	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73908146	ACCAGAAGTCATGTC[C/G]TTTTTTCAAATGGGG	80227
rs773387650	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73893731	ACAAAAGTGAAACTC[-/T]TGTCTCCAAAAAAAA	80227
rs773452572	snp	A/G	1.64866e-05	0.00287106	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887304	TCTTCAAAGAGAAAA[A/G]TAATAAATTTTTCTT	80227
rs773625400	snp	A/G	1.65067e-05	0.00287282	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900348	GTCCTGAGTGGGGGA[A/G]TGGATGCCCAGCTGA	80227
rs773675190	snp	A/G	1.76058e-05	0.00296692	intron-variant	PAAF1	GRCh38.p7	11:73900242	ATGGACAAGAGAACT[A/G]GCATGGAATTTTCTT	80227
rs773848672	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73899012	ACCTTTACATCAAAC[A/G]CAAGTCCTTTTGTTG	80227
rs773864562	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73901423	CAAGTTTGAATATTT[A/T]AAAAATATGTGATAA	80227
rs773929541	snp	C/T	1.65195e-05	0.00287393	intron-variant	PAAF1	GRCh38.p7	11:73909392	GGGAGTTTTTTTCTC[C/T]TGCTAGGTATCCTGG	80227
rs773955502	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73914025	TGTGAATGGCCCCTG[C/T]ACTCCAGCCTGGACA	80227
rs773966424	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875253	GAGAAATGACTTCAG[C/T]CTTTGCAAAAATTTC	80227
rs774062055	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909460	TGCTTCTCGAGATGG[A/G]ACAGCACGACTTTGG	80227
rs774067420	snp	A/G	4.98045e-05	0.00498997	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887442	AGAAGGATTTACTGT[A/G]AATGAAATAAACAAG	80227
rs774090181	in-del	-/AGA			intron-variant	PAAF1	GRCh38.p7	11:73886056	GAATATATAAGGTGT[-/AGA]AGAAGAATGGAAACA	80227
rs774144898	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73886158	TGCAAAATCAGTATT[-/C]TACTTAGGCAAATTT	80227
rs774147476	in-del	-/AAC	1.64921e-05	0.00287155	cds-indel, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916628	GGGACTCAAGATGGA[-/AAC]AACATTTATCAGCTG	80227
rs774183952	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73901567	GTTTTTGTGAACCTC[A/G]GTACATTGTAACTTG	80227
rs774275693	in-del	-/TA			intron-variant	PAAF1	GRCh38.p7	11:73908363	GTATATATGTGTGTA[-/TA]TATATATATGTATAT	80227
rs774389880	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73917049	TTTTTGAGATGGAGT[C/T]TCCCTCTGTCGCCCA	80227
rs774436179	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73920643	GGATTCCTTGAGGTC[A/G]GGAATTTGAGACTAC	80227
rs774452954	snp	C/T	1.7367e-05	0.00294673	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927404	GTGAAAAGGTTTGAC[C/T]CTGATCAACAATGAG	80227
rs774484773	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878440	TATTGTGAGGGTTAA[C/T]GATTGTGTATGGAAA	80227
rs774574102	snp	C/T	3.2962e-05	0.00405954	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909574	CTCCATAAACCTTGG[C/T]TCCCCTGAGCAGATG	80227
rs774707299	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73920698	TCTCTACTAAAAATA[C/T]AGAAATTAGCTGGCA	80227
rs774742296	in-del	-/C			intron-variant	PAAF1	GRCh38.p7	11:73903452	CCGGGCACTGTGGCT[-/C]ATGCCTGTAATCCTA	80227
rs774752747	snp	G/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924628	AGGTGATGGAAGCTG[G/T]TTTATTGTCCAGCAA	80227
rs774760647	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73895230	ATGATTCAAAAAATT[G/T]TGGCCTGAGAAGTAG	80227
rs774768370	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73905152	AAAACAAAAATAACA[A/G]TAAAGCTTTTTGCAG	80227
rs774815427	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73896254	GAAATATCTGAACTC[-/T]TTTTTTTTTTTTTTT	80227
rs774829882	snp	C/T	3.29592e-05	0.00405938	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918994	GAGCACCAGTTCTAT[C/T]CCTGCTAAGTGTCAG	80227
rs774843277	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888575	TTTTTGTGTAATTAA[A/G]CTTTTTAGTTATAAA	80227
rs774914382	snp	C/T	6.76453e-05	0.00581533	utr-variant-3-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927380	TCTTGGAAAGAGCAG[C/T]CCCGGTTAGTGAAAA	80227
rs774934906	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73889988	TTTGACTTTGAAACC[A/G]TTCTTTCTAATGAAC	80227
rs774952455	snp	C/T	1.66502e-05	0.00288527	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73899150	TCTTTGAACAGATAA[C/T]ATGCCTGGACATTTC	80227
rs775025887	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877635	TCATGCCTGTAATCC[A/C]AGCACTTTGGAAAAC	80227
rs775034573	snp	C/T	5.02896e-05	0.00501421	intron-variant	PAAF1	GRCh38.p7	11:73909362	TGTAGTTCCTTTACT[C/T]CATCCTCCATCTTAG	80227
rs775054434	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884251	CACCCTGTAATCCAA[A/G]CACTTTGGGAGGCTG	80227
rs775096547	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73903439	AAAAAATCTTGGTCC[A/G]GGCACTGTGGCTCAT	80227
rs775111686	snp	G/T	1.65501e-05	0.00287659	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900386	GTCAGCTGAAGATGC[G/T]AGCTGCGTGGTGACC	80227
rs775138421	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902426	AAGTAGTCTAGAGGA[A/G]CAGTGCAAGCTTCAC	80227
rs775153595	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73879732	AAAAAAATTAGTCAG[A/G]CATAGTGGCATGCGC	80227
rs775196655	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73920226	ATAATATTTTTTATA[A/T]ATTTTTTTAATTTAA	80227
rs775307266	snp	A/C	1.65438e-05	0.00287605	intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73924736	ACCTGGGTGATTCTC[A/C]TGAGAGATCTAGGGC	80227
rs775318362	snp	A/C	3.30644e-05	0.00406585	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878871	GGAGAAGGATTAATA[A/C]CCTTAAAAGAAAGCT	80227
rs775560816	snp	G/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886472	CGAGGTCAGGAGATC[G/T]AGTCCATTCTGGCTA	80227
rs775648867	snp	G/T	1.64822e-05	0.00287068	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73918975	CAAGTCATCCACAGA[G/T]CAGGAGCACCAGTTC	80227
rs775712125	in-del	-/TGT			intron-variant	PAAF1	GRCh38.p7	11:73881640	AAGCAACAAACTTAA[-/TGT]TGTTGTTGTTGTTGT	80227
rs775730977	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73880295	ACACACAAATACACA[A/G]ATATATATATATACA	80227
rs775766800	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890238	CATATTGCAAGAGTC[C/T]TTGAGGGAGGGTTTA	80227
rs775843814	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73898485	CCTCCCAGAGTGTTG[G/T]GATTACACAGGTGTG	80227
rs775872174	in-del	-/CT	1.70129e-05	0.00291653	intron-variant	PAAF1	GRCh38.p7	11:73914552	AGGCAACCTGGGTCA[-/CT]CTGTGTCTTAGAAAG	80227
rs775878348	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73906500	GAGTGATCTGCCCGC[C/T]TCAGACTCCCAAAGT	80227
rs775917968	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891072	TATAATACATTGGAG[A/G]AGTTTTACTGATGAA	80227
rs775924556	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875420	TAAGTTCCTGGCTTC[A/G]TGGAGTTTACAACCT	80227
rs775960411	in-del	-/AG	3.14549e-05	0.00396566	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887296	GAATTGGGTCTTCAA[-/AG]AGAAAAATAATAAAT	80227
rs776020038	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73912945	GCAGTGGCACGTTCT[C/T]GGCTCACTGCAACCT	80227
rs776053213	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902718	ATTATTTTTTTTGAG[A/G]TGGAGTCTCACTCTG	80227
rs776173984	in-del	-/AAAAAAAA			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73886673	GCAAGACTCCATCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA	80227
rs776242790	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924670	TGTCACTGAGCTCAC[C/T]GGGGCTGACTGTGAC	80227
rs776244289	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73882342	TTTGAAGGTAACTTG[G/T]AGATTCAGTTTTCTT	80227
rs776274696	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73911687	GGAGTGCAGTGGTGC[A/G]ATCTCTTGGCTCACT	80227
rs776295828	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73925278	CCTAGGCAATAAGAT[A/G]AGACCCCCGTCTCTA	80227
rs776312744	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73924284	ACATGGTGAAACCCC[A/G]TCTCTACAAAAATTA	80227
rs776343282	snp	A/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909563	GCTGCTGACAACTCC[A/G]TAAACCTTGGCTCCC	80227
rs776418433	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73903738	AAAAAAAATCTCTTA[C/T]GAGATTTTGAAGCAT	80227
rs776467420	snp	A/G	1.64887e-05	0.00287125	splice-acceptor-variant, intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878778	TTGTCTTTCTTCGTA[A/G]GAAGGATGAAGGGGA	80227
rs776526648	snp	A/G	9.95405e-05	0.0070541	intron-variant	PAAF1	GRCh38.p7	11:73909612	AGTTGATAATGATAT[A/G]TAGCATTGTTTTATT	80227
rs776530559	snp	A/G			intron-variant, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73888861	TAAAGCTGAGATCCT[A/G]TTCTACCTCCTAGAA	80227
rs776553988	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73894807	CCAGCCTGTGTTACT[C/G]AGCAAGACTCTGTCT	80227
rs776624432	snp	A/G	1.72621e-05	0.00293781	intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887493	GATGGCATGATATTT[A/G]AAACTATGGTAGTAC	80227
rs776657726	snp	G/T	1.64912e-05	0.00287147	intron-variant	PAAF1	GRCh38.p7	11:73914398	TGTTATTAACATAGT[G/T]TATTTGTCATGCAGG	80227
rs776764830	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73891242	AAAATGTAATAGCAT[A/G]TTAATTTTTCATTTT	80227
rs776848342	snp	G/T	1.65021e-05	0.00287241	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916555	CCCAGGTGTTCCTCT[G/T]TATTGGCTCAGACGC	80227
rs776903258	snp	A/T	1.67072e-05	0.00289021	intron-variant	PAAF1	GRCh38.p7	11:73916673	AAGGTGAGTCACCAT[A/T]CATTTACATGATGCA	80227
rs776916751	snp	A/G	4.95536e-05	0.00497738	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900374	GCTGAAGATATGGTC[A/G]GCTGAAGATGCTAGC	80227
rs776945209	snp	C/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875655	GTTGAGATAGAATCT[C/G]ACACATGAGAGCAAA	80227
rs776947006	snp	C/G	1.79677e-05	0.00299725	missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73891139	ATTTCATGTCCAAAG[C/G]AAAATGCATCTTCTA	80227
rs776948523	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73926113	CTTTCTTTCTTTCTT[-/T]TCTTTTTTTTGAGAT	80227
rs776979896	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877100	AACAGAGTCAGAGGA[C/G]GCGGGTAGTGGATGT	80227
rs777028255	in-del	-/TGT			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925197	CTTCTGGCTGACAGC[-/TGT]TGTAACCCCAGCACT	80227
rs777031354	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73892911	GTGATCCGCCCACCT[C/T]GGCCTCCCAGAGTGC	80227
rs777099387	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887584	GAATCATAGTTTTTG[C/T]TGTCTGTGAGTGTCA	80227
rs777219265	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73914803	ACCTCCACCTCCTAG[A/G]TTCAAGTGATTCTCC	80227
rs777339475	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890284	TTTTTTACCTCTACA[C/T]GTGCTACCTTCAAAC	80227
rs777356011	snp	C/G			downstream-variant-500B	PAAF1	GRCh38.p7	11:73928200	GCATTCCAGGTGATT[C/G]TGATGTATGCTAAAG	80227
rs777383612	in-del	-/AT			intron-variant	PAAF1	GRCh38.p7	11:73908255	TATATGTGTATATAT[-/AT]GTATATATGTGTATA	80227
rs777454726	snp	A/G	1.64982e-05	0.00287208	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73914491	AGTGCTTGGGACTAC[A/G]GAGCAGGCAGCTGGC	80227
rs777462433	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73875149	ACTATACAAAAATGT[A/G]AGGTGTATTTATTTG	80227
rs777510591	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73890860	TGTCTGTCTTCTGTG[C/G]AGCAGCTTATTTCAA	80227
rs777518213	in-del	-/T			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877175	GGGTTACTTCGTCAA[-/T]TTGTCGAGGGATATG	80227
rs777541204	snp	A/C	3.29679e-05	0.00405991	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878826	ATCCCCCAGGTAATA[A/C]CCATGAATTATATAT	80227
rs777603917	snp	C/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876696	TGCGCGCGCGCGGCC[C/G]CTGATCGCAGCCCCG	80227
rs777649513	snp	C/T	3.35554e-05	0.00409592	intron-variant	PAAF1	GRCh38.p7	11:73924573	TTTAAACTCTGGATG[C/T]AGTTTTCTCTTAGTT	80227
rs777663009	in-del	-/GTG	4.95352e-05	0.00497646	cds-indel, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900330	TTCCCATCAGGCCTT[-/GTG]GTCCTGAGTGGGGGA	80227
rs777705677	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73909177	ACTAAAAATTAAATC[C/T]AGTACTTGTTTTTCC	80227
rs777770609	in-del	-/AAG			intron-variant	PAAF1	GRCh38.p7	11:73919548	GGCAAGCGGGGGCAA[-/AAG]AAGAAGAGCACTAGC	80227
rs777860415	snp	C/T			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887782	TGAGATGGAGTCTTG[C/T]TCTGTCGCCCAGGCT	80227
rs777872031	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73922920	CAGATGAAACAAAAT[-/A]AAAAAACAAAATTTT	80227
rs777966009	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73898971	GTTTACTTCAGCCTT[G/T]TTGGGAGGTTGGTGA	80227
rs777987378	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73911084	TATCAATATCCCCCA[C/G]CAGAGTGGTACATTT	80227
rs778042818	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73924147	TTCTAGGCAGCCACT[A/G]TAGATCATCATAATT	80227
rs778158196	snp	A/G	1.65211e-05	0.00287407	synonymous-codon, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927293	GTTTTAGGTAGCCAC[A/G]TGGGAGAAGCAGATC	80227
rs778282499	snp	C/G	1.65886e-05	0.00287993	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73927352	GACGCTACCAGCTTT[C/G]TGACCTCTGACTTCT	80227
rs778307529	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73890942	ACAGTTTAAAAGGAC[C/T]GCTGATCTATGGGGG	80227
rs778402095	in-del	-/AT			intron-variant	PAAF1	GRCh38.p7	11:73884511	ATATTAAAAAAATAC[-/AT]ATATATATACATCCA	80227
rs778455225	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73892183	ACAAAAATTAGCCAG[A/G]CATGGTGCCACATGT	80227
rs778504299	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73907441	GTCCTGTGTCATCTT[C/T]TTGGTGAAAGTAGGA	80227
rs778506070	snp	C/T	1.67063e-05	0.00289014	intron-variant	PAAF1	GRCh38.p7	11:73916670	TCCAAGGTGAGTCAC[C/T]ATTCATTTACATGAT	80227
rs778677362	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73902268	TGGTTTACTTCCATG[A/G]TGTAAGAAAACGGGT	80227
rs778739970	snp	A/G	9.88452e-05	0.00702942			GRCh38.p7	11:73909541	TATCAATGGAGTGGC[A/G]GTGGGTGCTGCTGAC	80227
rs778740445	snp	C/T	1.98088e-05	0.00314707			GRCh38.p7	11:73891102	ATCTCATCTTTTCCT[C/T]TTTGTTTAGAAAAGC	80227
rs778761043	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73903151	TTTTAGTAGATTGAA[C/T]GGAATGATATACTTT	80227
rs778761868	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73916208	TGGGAATTGCAAGTG[G/T]TTCTCAGAAAGTTGT	80227
rs778791683	snp	C/T	1.6473e-05	0.00286988	intron-variant	PAAF1	GRCh38.p7	11:73899105	AGGGAATAAGAGTAT[C/T]TCATTATTTCTAACA	80227
rs778827525	snp	A/T	1.65353e-05	0.00287531	intron-variant	PAAF1	GRCh38.p7	11:73918944	TCCCCTTTCTCTGAA[A/T]CCTAGGGCTCCGGTA	80227
rs778852527	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877630	GTGGCTCATGCCTGT[A/G]ATCCCAGCACTTTGG	80227
rs778853997	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73886115	GTGTGTTTATGTGTA[A/G]GATAGTATCTTACTT	80227
rs778972045	snp	C/G	5.13395e-05	0.00506627	intron-variant	PAAF1	GRCh38.p7	11:73900440	GAAGTGTGCTTTCTC[C/G]AAAAGGCTTCTCTAA	80227
rs779028916	in-del	-/CC	1.70542e-05	0.00292007	intron-variant	PAAF1	GRCh38.p7	11:73927246	TTGAAATGGAAGAAT[-/CC]CCCAGGCTTCCTTTG	80227
rs779052069	snp	C/T			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874941	TAGTGAGCCAAAGAT[C/T]GTGCCACTGCACTCC	80227
rs779057893	snp	A/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	PAAF1, COA4	GRCh38.p7	11:73876799	CGCACGCTCCTACGC[A/G]GCGGCTTGGGTTTCG	80227
rs779115471	snp	C/T	8.25416e-05	0.00642371	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73900337	CAGGCCTTGTGGTCC[C/T]GAGTGGGGGAATGGA	80227
rs779121243	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73883648	CAGCCTCCTGAGTAG[C/T]TGGGATTACAGGCGC	80227
rs779128477	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73912289	AGACTCTATTTCGAT[G/T]TCTAATAAATAAGTT	80227
rs779129896	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73895834	AAGTGAGGCTGGGCG[C/T]GGTGGCTCACGCCTG	80227
rs779152413	in-del	-/AC			intron-variant	PAAF1	GRCh38.p7	11:73880308	CAAATATATATATAT[-/AC]ACACACACATATACA	80227
rs779181342	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73911379	GTAGAGACAGGGTCT[C/T]ACTATGTTGCCCAGG	80227
rs779208612	in-del	-/T	1.64735e-05	0.00286993	frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73909477	AGCACGACTTTGGGA[-/T]TTGTGGGCGCTCAGC	80227
rs779231695	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919977	AAAGAGACTAAGGAA[A/G]CTTGACAACTAAGTC	80227
rs779271606	snp	A/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916557	CAGGTGTTCCTCTTT[A/T]TTGGCTCAGACGCTT	80227
rs779280266	snp	A/G	3.30748e-05	0.00406649	intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878747	TATTCAACTTTGGGT[A/G]AGCCTAATTAGGCTT	80227
rs779321779	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73921197	CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	80227
rs779395956	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73885441	GCCACCATGCCCGGC[C/T]GACTTTCTTTTATTC	80227
rs779488710	snp	C/T	2.18577e-05	0.00330581	intron-variant	PAAF1	GRCh38.p7	11:73891077	TACATTGGAGGAGTT[C/T]TACTGATGAATCTCA	80227
rs779589240	in-del	-/AA			intron-variant	PAAF1	GRCh38.p7	11:73893750	CTCCAAAAAAAAAAA[-/AA]AAAAAAAAAAGAAAG	80227
rs779589918	snp	A/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73877780	AATCCCAGCTACTCG[A/G]GAGGCTGAGGCAGGA	80227
rs779600152	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73915384	GCCCAGAAAGGGTGG[A/G]TTGCTTGAGTCCAGG	80227
rs779607197	snp	A/G	2.19952e-05	0.00331619	intron-variant	PAAF1	GRCh38.p7	11:73891229	ATAAAATGAAGAGAA[A/G]ATGTAATAGCATGTT	80227
rs779702531	in-del	-/GAGGGAGAGGGA			intron-variant	PAAF1	GRCh38.p7	11:73898218	GGGGAGGGGAAGGGG[-/GAGGGAGAGGGA]GAGGGAGAGGGAGAG	80227
rs779722763	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73905987	AGGATTCTTAAAAGC[G/T]CTAAGATACTTTCTA	80227
rs779735822	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73903320	CTGATAGCTTAACAG[C/T]GTATATATAGATAGA	80227
rs779848077	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919817	GCATTTCAGTATGTC[A/G]GTTAGGATGTTTTGG	80227
rs779901027	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73892859	TAGAGACGGGGTTTC[A/T]CTGTGTTAGCCAGGA	80227
rs779917032	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73907442	TCCTGTGTCATCTTC[-/T]TGGTGAAAGTAGGAC	80227
rs779934729	snp	A/T	1.65151e-05	0.00287355	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916645	ACATTTATCAGCTGG[A/T]TGTGAGGAGTCCAAG	80227
rs779964806	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73900554	TTAGATGAGCTGCCA[C/T]TTCCCTAAGGACCAG	80227
rs780110898	snp	C/T	1.70359e-05	0.0029185	intron-variant	PAAF1	GRCh38.p7	11:73927248	TGAAATGGAAGAATC[C/T]CAGGCTTCCTTTGAA	80227
rs780141111	snp	A/G	3.2962e-05	0.00405954	utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73878804	GGGGAGGCCTGGCTG[A/G]GCTGTCATCCCCCAG	80227
rs780301766	snp	A/G	1.75888e-05	0.00296548	intron-variant	PAAF1	GRCh38.p7	11:73899269	TTGGATGTACTTTTA[A/G]GTCTTAAACACAAAG	80227
rs780342463	snp	A/G	1.66134e-05	0.00288208	intron-variant	PAAF1	GRCh38.p7	11:73924589	AGTTTTCTCTTAGTT[A/G]TATGAATTTTCTTTC	80227
rs780392910	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73907661	GTCAACCCCACTGGG[G/T]AGGGGAATGGGAGTG	80227
rs780506637	snp	A/G	1.66275e-05	0.00288331	intron-variant	PAAF1	GRCh38.p7	11:73914520	GCAAGTGGTTCCTAT[A/G]TGACCTTTGAACTCT	80227
rs780581051	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73900527	ACACAAATAATCCAT[C/T]CAGCTGGGCATTTAG	80227
rs780631254	snp	A/G	6.59478e-05	0.00574191	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	PAAF1	GRCh38.p7	11:73887396	CTTGTCAAGGAATTG[A/G]CCTAGATGGCATCCC	80227
rs780757229	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73893357	ATTGTAATGCCAGTT[-/A]ATATTATTTTTGAAA	80227
rs780819586	snp	A/C	6.59587e-05	0.00574239	missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73916624	TGGCTGGGACTCAAG[A/C]TGGAAACATTTATCA	80227
rs780871147	snp	G/T	0.000790201	0.0198614	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	PAAF1	GRCh38.p7	11:73889175	CTTCATACTCAGACC[G/T]GGATACAGTCTTTAT	80227
rs781013767	snp	A/T			intron-variant	PAAF1	GRCh38.p7	11:73890607	CAATTTCATCTGGTC[A/T]TTGTAAATGTCAGTA	80227
rs781062125	snp	A/C			intron-variant, upstream-variant-2KB	PAAF1	GRCh38.p7	11:73887184	CAGACTAAGACACCT[A/C]ATCTAATTCTCTTTT	80227
rs781118042	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73912422	CAAAGCCTGAGATTC[A/G]CTCACAGTCCACCCT	80227
rs781158504	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73902067	ATGGGGTTTCGCTGT[G/T]TTGGCTGGGCTGGTC	80227
rs781166373	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73911622	CACCAGTGACCTTCC[-/T]TTTTTTTTTTTTTTT	80227
rs781250049	snp	A/G	0.000952532	0.0218027	utr-variant-5-prime, intron-variant, upstream-variant-2KB, missense, nc-transcript-variant	PAAF1, COA4	GRCh38.p7	11:73877067	TGGGCGCAAGCCCTC[A/G]GGTGAATCCAGGCCC	80227
rs781251422	snp	A/G			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73874928	GGGGCGGAGGTTGTA[A/G]TGAGCCAAAGATCGT	80227
rs781284036	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73921871	GGAAAACCAGGTTCT[C/T]CAGGAATGGGAAAGT	80227
rs781313034	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73893140	TTTTTATGAATACAT[C/T]TATAGCTAAAGTTTT	80227
rs781406902	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73910519	ATGGGTTGAATAGCT[A/G]TGGTGAGAGACTAAT	80227
rs781552454	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73919925	CAGAGTCCATTTCAG[A/G]TTATATTAATTTAGT	80227
rs781623448	snp	C/G			intron-variant, upstream-variant-2KB	PAAF1, COA4	GRCh38.p7	11:73878037	GCTACTACTAATAAG[C/G]GTTTTTCAAATTGAA	80227
rs781714124	snp	C/G			intron-variant	PAAF1	GRCh38.p7	11:73879523	GAAAGTTTTGTTTTG[C/G]TGATTATCTTTCATT	80227
rs796143029	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73910060	TAGAGAACAGTAACA[-/T]TTGGCTGAAATAATT	80227
rs796189326	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73897079	CGCCCCTCACCTCCC[A/G]GACGGGGCGGCTGGC	80227
rs796193554	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73884883	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	80227
rs796250321	snp	G/T			missense, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924653	CAGCAAGACTTAGAC[G/T]ATGTCACTGAGCTCA	80227
rs796306693	snp	A/C			intron-variant, downstream-variant-500B	PAAF1	GRCh38.p7	11:73925176	AAAAAAAAAAAAAAA[A/C]AAGTGACTTCTGGCT	80227
rs796334064	in-del	-/A			upstream-variant-2KB, intron-variant	PAAF1, COA4	GRCh38.p7	11:73876141	CAAAAAAAAAAAAAA[-/A]GAAAAAAAAAAAGGT	80227
rs796349252	in-del	-/TA			frameshift-variant, nc-transcript-variant	PAAF1	GRCh38.p7	11:73924648	TTGTCCAGCAAGACT[-/TA]GACTATGTCACTGAG	80227
rs796353778	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73918363	CTTAATTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	80227
rs796432942	snp	A/G			intron-variant	PAAF1	GRCh38.p7	11:73893758	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAAC	80227
rs796486704	in-del	-/AG			intron-variant	PAAF1	GRCh38.p7	11:73901086	TGTGTGCTGGGAAAT[-/AG]AGAGAGAGAGAGTGA	80227
rs796514515	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73900002	AAAGCCATGGAATTC[-/T]TTTTTTTTTTTTTTA	80227
rs796579769	in-del	-/A			intron-variant	PAAF1	GRCh38.p7	11:73903730	TCAAAAAAAAAAAAA[-/A]TCTCTTATGAGATTT	80227
rs796612922	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73912032	CTCTCCTCAAAAAAC[-/T]TTTTTTTTTCATGGC	80227
rs796629251	in-del	-/ACTTA			intron-variant	PAAF1	GRCh38.p7	11:73907636	CTGTGACAGTACCCT[-/ACTTA]ACCTGGTCAACCCCA	80227
rs796635145	in-del	-/T			intron-variant	PAAF1	GRCh38.p7	11:73881883	GGCTAATTTTTTGTA[-/T]TTTTTTTTGAGATGG	80227
rs796639337	snp	C/T			intron-variant	PAAF1	GRCh38.p7	11:73924413	ATCATGCCATTGTAC[C/T]CTAGCCTGGGCAAAA	80227
rs796806415	snp	G/T			intron-variant	PAAF1	GRCh38.p7	11:73880011	TGGGAGGCCAAGGCG[G/T]AGGATTGCTTGAGAC	80227
rs796857177	multinucleotide-polymorphism	AA/GG			intron-variant	PAAF1	GRCh38.p7	11:73880688	AAGACTCTGTCTCGA[AA/GG]AAAAAAAAAAAAAAA	80227

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